CRISPRimmunity

Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP010833	Streptomyces sp. Tue 6075 strain Tue6075 chromosome, complete genome	23 crisprs	csa3,DEDDh,DinG,cas3,WYL,cas8e,cse2gr11,cas7,cas5,cas6e,cas1,cas2,cas4	9	54	2	0

1. NZ_CP010833

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP010833_1

• CRISPR_ID: NZ_CP010833_1
• CRISPR_location: 26976-27060
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: csa3

Consensus repeat of NZ_CP010833_1

Consensus_repeat	Method
CGTAGTGCTCTCCGCGCGAGCGGAG	CRISPRCasFinder

spacers of NZ_CP010833_1

>1.1|27001|34|NZ_CP010833|CRISPRCasFinder
GTGGCCACCCGGAGGCCACGGACACCGTGACCGG

CRISPR arrays and Neighbor proteins around NZ_CP010833_1

CRISPR arrays

The CRISPR arrays of NZ_CP010833_1

>merge|NZ_CP010833|1|26976-27060|CRISPRCasFinder
CCACGTGCTCTCCGCGCGAGCGGAGGTGGCCACCCGGAGGCCACGGACACCGTGACCGGTCGGGTGCTCTCCGCGCGAGCGGAGA

>NZ_CP010833|1|1|26976-27060|CRISPRCasFinder
CCACGTGCTCTCCGCGCGAGCGGAG	GTGGCCACCCGGAGGCCACGGACACCGTGACCGG
TCGGGTGCTCTCCGCGCGAGCGGAGA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075262739.1|17100_18387_-|hypothetical-protein	unknown	unknown	gnl|CDD|224588
NZ_CP010833.1|WP_079181388.1|35589_36105_-|HAD-hydrolase-like-protein	unknown	unknown	gnl|CDD|319809
NZ_CP010833.1|WP_075262751.1|31246_31690_-|polyketide-cyclase	unknown	unknown	gnl|CDD|176909
NZ_CP010833.1|WP_075262740.1|18404_18584_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262759.1|38032_38416_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262753.1|32433_32655_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_159027389.1|14648_15626_+|hypothetical-protein	unknown	unknown	gnl|CDD|376279
NZ_CP010833.1|WP_075262745.1|24294_24852_+|DNA-binding-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262744.1|22173_24291_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|238045
NZ_CP010833.1|WP_079181386.1|26397_26787_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262741.1|18818_19655_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl|CDD|223713
NZ_CP010833.1|WP_075262749.1|29534_30536_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381378
NZ_CP010833.1|WP_159027390.1|21948_22110_+|hypothetical-protein	unknown	unknown	gnl|CDD|367510
NZ_CP010833.1|WP_075262755.1|34904_35606_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262750.1|30821_31250_-|SnoaL-like-domain-containing-protein	unknown	unknown	gnl|CDD|226769
NZ_CP010833.1|WP_079181385.1|15694_16423_+|DUF4145-domain-containing-protein	unknown	unknown	gnl|CDD|372658
NZ_CP010833.1|WP_075262754.1|33841_34438_-|hypothetical-protein	unknown	unknown	gnl|CDD|215059
NZ_CP010833.1|WP_075268175.1|16639_16891_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262748.1|29035_29515_-|hypothetical-protein	unknown	unknown	gnl|CDD|379151

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	1.1e-15	52.7	0.5

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075262739.1|17100_18387_-|hypothetical-protein	gnl|CDD|224588	COG1674, FtsK, DNA segregation ATPase FtsK/SpoIIIE and related proteins [Cell division and chromosome partitioning].	0.000337943
NZ_CP010833.1|WP_159027390.1|21948_22110_+|hypothetical-protein	gnl|CDD|367510	pfam03457, HA, Helicase associated domain. This short domain is found in multiple copies in bacterial helicase proteins. The domain is predicted to contain 3 alpha helices. The function of this domain may be to bind nucleic acid.	0.000106453
NZ_CP010833.1|WP_079181388.1|35589_36105_-|HAD-hydrolase-like-protein	gnl|CDD|319809	cd07506, HAD_like, uncharacterized family of the haloacid dehalogenase-like (HAD) hydrolase superfamily. The haloacid dehalogenase-like (HAD) hydrolases are a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members include 2-L-haloalkanoic acid dehalogenase (C-Cl bond hydrolysis), azetidine hydrolase (C-N bond hydrolysis); phosphonoacetaldehyde hydrolase (C-P bond hydrolysis), phosphoserine phosphatase and phosphomannomutase (CO-P bond hydrolysis), P-type ATPases (PO-P bond hydrolysis) and many others. Members are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	2.29208e-12
NZ_CP010833.1|WP_159027389.1|14648_15626_+|hypothetical-protein	gnl|CDD|376279	pfam18860, AbiJ_NTD3, AbiJ N-terminal domain 3. Alpha + beta domain. Found fused to AbiJ-like HEPN. Fused to other domains presumably involved in defense.	0.00700082
NZ_CP010833.1|WP_075262750.1|30821_31250_-|SnoaL-like-domain-containing-protein	gnl|CDD|226769	COG4319, COG4319, Ketosteroid isomerase homolog [Function unknown].	9.14713e-17
NZ_CP010833.1|WP_075262744.1|22173_24291_+|helix-turn-helix-domain-containing-protein	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	7.28547e-08
NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|223713	COG0640, ArsR, Predicted transcriptional regulators [Transcription].	8.93066e-11
NZ_CP010833.1|WP_075262749.1|29534_30536_-|aldo/keto-reductase	gnl|CDD|381378	cd19152, AKR_AKR15A, AKR15A family of aldo-keto reductase. The AKR15 family includes Microbacterium luteolum pyridoxal 4-dehydrogenase (PLD), Pseudomonas sp. D-threo-aldose 1-dehydrogenase (FDH), and similar proteins. PLD (EC1.1.1.107) catalyzes irreversible oxidation of pyridoxal. FDH(EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose. FDH (EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose.	9.52791e-108
NZ_CP010833.1|WP_075262754.1|33841_34438_-|hypothetical-protein	gnl|CDD|215059	PLN00111, PLN00111, accumulation of photosystem one; Provisional.	0.00394884
NZ_CP010833.1|WP_075262751.1|31246_31690_-|polyketide-cyclase	gnl|CDD|176909	cd08900, SRPBCC_CalC_Aha1-like_7, Putative hydrophobic ligand-binding SRPBCC domain of an uncharacterized subgroup of CalC- and Aha1-like proteins. SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of a functionally uncharacterized subgroup of CalC- and Aha1-like proteins. This group shows similarity to the SRPBCC domains of Micromonospora echinospora CalC (a protein which confers resistance to enediynes) and human Aha1 (one of several co-chaperones which regulate the dimeric chaperone Hsp90), and belongs to the SRPBCC domain superfamily of proteins that bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands.	6.95583e-49
NZ_CP010833.1|WP_079181385.1|15694_16423_+|DUF4145-domain-containing-protein	gnl|CDD|372658	pfam13643, DUF4145, Domain of unknown function (DUF4145). This domain is found in a variety of restriction endonuclease enzymes. The exact function of this domain is uncertain.	1.6799e-10
NZ_CP010833.1|WP_075262748.1|29035_29515_-|hypothetical-protein	gnl|CDD|379151	pfam13378, MR_MLE_C, Enolase C-terminal domain-like. This domain appears at the C-terminus of many of the proteins that carry the MR_MLE_N pfam02746 domain. EC:4.2.1.40.	1.08212e-37

Protein sequences

>NZ_CP010833.1|WP_079181386.1|26397_26787_+|hypothetical-protein
MAYVPQFRRDVLDTAAWLRSGEGSPLPFAGLSAEATHRRLMQRAGDDDEPEADYQLRGRFRVLLWGPTTDNVTAYLFRQEDHLVITLSFWREEHLLSHPEDAGTVFVVEIPAKEFVGILEGIAAALGTS
>NZ_CP010833.1|WP_075262745.1|24294_24852_+|DNA-binding-protein
MGEIEDAIERADRESFTREPPKTLKGQIGYLLKQMGSAKAVAAELGVTADSVNRYRRGARRHARADVAAKIDDAVRQRWQPMVRKRRQKQAAASGGITVETRARFGYTSSAGSTDDGRFRRLTVKLPATYAQRLFDARDTGASDQQMRQIIAEGFKEIYFQDGGGRAAGLSDVTLNDIDYLDVDY
>NZ_CP010833.1|WP_075262744.1|22173_24291_+|helix-turn-helix-domain-containing-protein
MASEEELFASVDALLEEEPQLPPPAERARLREAAGITQARLAVALKTSTQTVKNYENGRSEPKSPRLEAYQRLLKGWAAKYPAHASSAASAPAVAPQPEVPGTFTGSAAPEQAEAATPVQAPAAALAAPERPERSATSRRPAATTAAAPAVDPRFPHGPLAVLDGDGSAYGAGGIVLDCPATTIPELVEWTLRESGLGTAKLNRYGKDSDPLIVLTAAAAVKLGLPERLEGHEQRRSLRLPEDHPVVKQVAKAKWQLTQRGFGPWARIYRKAQGRERQCVQLAILSWDALDERSWPGVSEMEPADIARVLGVYAMRVITPRGSTAVSGLELMTALRPPTKAVRDEETGNWVSGHNAGSLGTEPMDPAPPEATPEHPVVVDSGWKGGFLNEEAYQWVRDVDTLSDEECTLPFAVGLDLNTAFLAAAARLVVGLSAPDHFHAPKFNPKIPGSWLADLSHIELDPRLPSPFTPDGTRPTGAAWYQTHTLAYAQELGHDVHPIEAYLRRETGAYLDPWHDRLKNAYVDTLADMGVTKDLNDVGFLAAMEQHKQNDPALAAVLSAIKATVKGGVGKLRERPQGKSYKEGETWPALSRPTWRPDIRAAVISKARVNMHRKLNNMVKMTGLYPLAVLSDCVVYPSPGESPIDFLPYAASGKPQPGAFRLGPTPGLAKLEGVQSMLWAVDLMEKGLNPARHIKGGDAVMDEGE
>NZ_CP010833.1|WP_159027390.1|21948_22110_+|hypothetical-protein
MTVPRGHVEGVKVGGQEYPVKLGVWIMNQKGRRAKLTPDKLQALAALGLEWAR
>NZ_CP010833.1|WP_075262741.1|18818_19655_+|hypothetical-protein
MTNDFEAHLAATLGAATENIRQTMAASIRPAPKVELPTSLRETLAKAVAPLLPVLERLDAMMPGNWRGQHLDYERMVRLMQEGVPLAWVPPADVIRQLLAADDASSRSKVIDDSHPAILASCREALAEVTDARLTPQRTLLEECARAIENGMFNSAQALAANVWDTLMRGIAFANPDLLTSKGTWNYRHIRRNVPSVDAEEDATLGELRRAAVFLPVAKVLEDFWHPQPVPFGFNRHATAHAAGTVQYTASNAMTALMLAVSVLREIDDQAYVVHIHA
>NZ_CP010833.1|WP_075262740.1|18404_18584_-|hypothetical-protein
MARTKFDKQVDESADTFACGLARMLAGRDLDGVRRTDATFWRSGTRVLPKVEGKVRRRS
>NZ_CP010833.1|WP_075262739.1|17100_18387_-|hypothetical-protein
MSFRLTLCGGLAESGYLTTRDLDATGETLRDLTELWEHREAALAALEPAGIGAASVLTVGTAAYMVLTRERRELMRQWVGPLHEALHQPLGLAEQTDPRRYLHIPKNFSDDDAQIRIDLPTRLGFSRDVVADLITQKLALQGVTFSWHPEGRKPYVLVKKTRKPPAISLFKGPKTRELVAKAKEFAPVIGFGAGGRIVSVDLDAESPHILVNASTGGGKSVILRCIACQMLHHGSRVFVLDTKRISHLWAKALPTVTHRGNIAGIHDALLGLATELERRLDLDGDLDTVPRLIVAIDEANTTLPRLARYWETFRQKDDPKTSPAIAALEQALWFGRAARVHVIFDGRPQATVLRSAARELFATVILARFTTDTWQVLAPDAGPAPKQRHPQQGHFHVIQHGEVDETQAIRMTDADVVAWLTDPDDPTA
>NZ_CP010833.1|WP_075268175.1|16639_16891_-|hypothetical-protein
MRCGSADTRVTRLDPTSAEGTCFRCDKPFHATPCQNCGGFRIDGSFGASGTRFEILPETVRCWDCRHRNPLRDPGPEETASAR
>NZ_CP010833.1|WP_079181385.1|15694_16423_+|DUF4145-domain-containing-protein
MNEQELTSLEQRRAVCPYSDCATGTVMDMVDQRMLAPESREYALAEFGEEGEGALPVYPHSSWTQQECWVCQLCGRSILEVIECKKTGAGREARIEELTRLVLWPSPAPRVLDPDVPERIRSAYEEASRAENAGAARLAGVGYRSAVEELCKDQGATHKTLHGKIRELAAQGLPGDIITALDETRVVGNDSVHQGVAYSAEELADIAELVAEAAVLLYVQPAQRRRMAESRKKRHETAQQNP
>NZ_CP010833.1|WP_159027389.1|14648_15626_+|hypothetical-protein
MNLPSGVPVFKLRDAIAEALWGHVKANRLAAVCEYLGLAPQGADEDPYNSKRGYVLARLEDKSLPDLMDVARRVIKEYGDDDLQQLLAQLGLQGVSGELKNLIFAADGPKPQIVLPDSISNTIRIVKNEQYCLVYDQPLEGRGLSWQDLVTWWVRQHPEHADDPTQARISLRDRLRRSLGDNGAELLVFDTYVKLGFDLPALIPQVYLHYDPYSMSELGGARRLARQRMDFLLLMNHRARAVIEIDGIQHYARPADRAAGQRPDANWLADTGRYASMVAEDRELTLQGYEVYRIGGHELCDAAAPKMLTAFFERLLRRHDHTDSS
>NZ_CP010833.1|WP_075262748.1|29035_29515_-|hypothetical-protein
MAEDPATVDAVRDAGPALRIAVDAHRAYRPAQARKLAAALADRGCWFLEASLVPEDLDGHRRLAGHSPLPLAVGEALRNRYEFAHWLRAGALEIAQPDVTRTGITEAMAIAEISGAHHIPAAPHHSVGLGVALAAGLQVSIRAAHSACESNVMTSFHCF
>NZ_CP010833.1|WP_075262749.1|29534_30536_-|aldo/keto-reductase
MRADDPVSLGRTGLRVSRLGLGLASLGGLFAPVSDTQAAEVLERAWQLGIRLYDTAPVYGYGRSERRTGAALAGRPRDAFVLCTKVGRLIERGGPDTQPIWADPPEEMGPRKDYSFAGVMRSVAESLERLGMDRVDVLHVHDPDEEFGAAVGEAYRALAVLRDRGTIGAVSIGVNHAPVAARFLREAAAPGPDCVLLAGRYGLLDQSGLDELLPLCAERGVAVLAAGVYHGGLLTEPSPGTPHAHTTLPSRTTARIAGWQKLCSRFEVPLLAAAVQLPFGHPAVAAVLVGARTATQVEQSAAWLAHPVPTALWDQARRAGLLPAMCPIPTSCS
>NZ_CP010833.1|WP_075262750.1|30821_31250_-|SnoaL-like-domain-containing-protein
MTPDSERQIRDLLAARTRAFGRRDAATAAADYDDGLVLYDAVGPFVRRGEDQADRLERWIASYRTGIGHEIRDLEITAGTDLAFCHFLVRISGSMRDGTEVGMWVRATCCLRRMDDAWTIVHEHASVPFDADTGQAVLRGEL
>NZ_CP010833.1|WP_075262751.1|31246_31690_-|polyketide-cyclase
MTGHSVKHSTFTLERTYAAPPAAVFAAWSDRDRKAKWFAAGDGRYSLDFRVGGTEAVHGGDGTGLVARSAYHDIVLDERIVYTTALFTGEVLSTVSLTTVRFSPDGERTLLVLTEQGTFLDDQEQPQWREQGTGEWLDALGQEVDER
>NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator
MLKREVESADRVFHALADPNRRAMIERLTLGPAAVSELAAHLGVTLAATVQHLRVLQDSELVRSEKSGRVRTCRIDTSGLRDAEAWLQHQRTAWEHRLDRLGAVLDDQPKESES
>NZ_CP010833.1|WP_075262753.1|32433_32655_+|hypothetical-protein
MGRPLLPLRSALVPVMAVISGLVAGWLCWIAEGSVPRGDLAGLGAVGLAAPFFNRLLAAEAAERTGEEVRGRG
>NZ_CP010833.1|WP_075262754.1|33841_34438_-|hypothetical-protein
MRIATASAAATFCAAALALTFGTAVAVTPADGAPAEQAGGQPACGSVESYRLGAPYSGNINRNGNEMPVHLTPGAEQHRIGRISTGPVTGPATTPDGKTFTIENEWTALDDMITKAVANYQVRDADGVEVGKVTCDPATGAVTGVVAHDIDATFGGHELQTCESSICSGGSGAHSWTPERIDRHIVGTLTLTSDQAAN
>NZ_CP010833.1|WP_075262755.1|34904_35606_+|hypothetical-protein
MRFPRFNEDGPLVGYELEAMRSLSSAFLTARYEWQAACTMWDRLYTAGETAELRRSPASFSFYEEAVGRLAGGVRDYERQAALVAWRYTAASLVLGVTVLRRIAEGKPPLTVTGVEELCQEPALGQLHEALSVPVPDLVPERRHPADIPGDRECSAREWGTVREGVADVIDLVLELAIDEDAAHPRTRDEAATCLLTQHCPPHTEPVHDGVLQPLFQLAEQVPYGIARIIDHG
>NZ_CP010833.1|WP_079181388.1|35589_36105_-|HAD-hydrolase-like-protein
MRAGDADAGAATGHLIEYVNVPIGGYTSDSPHRPNLVGISQSRAVERHGKMFGSSNTVIIGDSLQDVTTGIEAGAKVIGVTSGTTSAQQLADAGAHLVIPGLRNSESLLSLIRSLSSQWHLAGAGPVAPTLPSSPFRLGFDALVSAPAERSRGVRHRAPSQTATRCFNRGR
>NZ_CP010833.1|WP_075262759.1|38032_38416_-|hypothetical-protein
MGLVLFPGDGDNSSPDVSWSYSGFAAFRQRLAEAEGFALSEMWGFGGERPWSEVSTALEPLLDHPDAGGDDLSPTECASVLIRLEAITDQWARKSGDQLHQQHIEDARQLAGILRLCIEKDVPLVFL

Crispr_ID: NZ_CP010833_2

• CRISPR_ID: NZ_CP010833_2
• CRISPR_location: 27744-28013
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 4 spacers
• Cas_protein_info: csa3

Consensus repeat of NZ_CP010833_2

Consensus_repeat	Method
GNGCTCTCCGCGCGAGCGGAGGTGAG	CRT
CGTAGTGCTCTCCGCGCGAGCGGAG	CRISPRCasFinder

spacers of NZ_CP010833_2

>2.1|27770|35|NZ_CP010833|CRT
CCAGTCCTCAGCTATTACGTAGCGCCAGGCAGTTC
>2.2|27831|35|NZ_CP010833|CRT
CCACGGCGTCTCACGTGCTCGTTGGCCCTCTCGTA
>2.3|27892|35|NZ_CP010833|CRT
CCGACCCGGCCGATGCGCTCGATCAGCACTGCGTC
>2.4|27953|35|NZ_CP010833|CRT
TCCTACCGCCTTAGCGGCAAGGGTGTGCCGCCCTT
>2.5|27826|36|NZ_CP010833|CRISPRCasFinder
GTAAGCCACGGCGTCTCACGTGCTCGTTGGCCCTCT
>2.6|27887|36|NZ_CP010833|CRISPRCasFinder
GTGAGCCGACCCGGCCGATGCGCTCGATCAGCACTG
>2.7|27948|36|NZ_CP010833|CRISPRCasFinder
ATGATTCCTACCGCCTTAGCGGCAAGGGTGTGCCGC

CRISPR arrays and Neighbor proteins around NZ_CP010833_2

CRISPR arrays

The CRISPR arrays of NZ_CP010833_2

>merge|NZ_CP010833|2|27744-28013|CRT,CRISPRCasFinder
TGGCTCACCACGCCAGCGGAGGTGAGCCAGTCCTCAGCTATTACGTAGCGCCAGGCAGTTCGTGCTCTCCGCGCGAGCGGAGGTAAGCCACGGCGTCTCACGTGCTCGTTGGCCCTCTCGTAGTGCTCTCCGCGCGAGCGGAGGTGAGCCGACCCGGCCGATGCGCTCGATCAGCACTGCGTCGTGCTCTCCGCGCGAGCGGAGATGATTCCTACCGCCTTAGCGGCAAGGGTGTGCCGCCCTTGCACTCTCCGCATGAGCGGAGGCGGG

>NZ_CP010833|2|1|27744-28013|CRT
TGGCTCACCACGCCAGCGGAGGTGAG	CCAGTCCTCAGCTATTACGTAGCGCCAGGCAGTTC
GTGCTCTCCGCGCGAGCGGAGGTAAG	CCACGGCGTCTCACGTGCTCGTTGGCCCTCTCGTA
GTGCTCTCCGCGCGAGCGGAGGTGAG	CCGACCCGGCCGATGCGCTCGATCAGCACTGCGTC
GTGCTCTCCGCGCGAGCGGAGATGAT	TCCTACCGCCTTAGCGGCAAGGGTGTGCCGCCCTT
GCACTCTCCGCATGAGCGGAGGCGGG

>NZ_CP010833|2|2|27801-28008|CRISPRCasFinder
GTTCGTGCTCTCCGCGCGAGCGGAG	GTAAGCCACGGCGTCTCACGTGCTCGTTGGCCCTCT
CGTAGTGCTCTCCGCGCGAGCGGAG	GTGAGCCGACCCGGCCGATGCGCTCGATCAGCACTG
CGTCGTGCTCTCCGCGCGAGCGGAG	ATGATTCCTACCGCCTTAGCGGCAAGGGTGTGCCGC
CCTTGCACTCTCCGCATGAGCGGAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075262739.1|17100_18387_-|hypothetical-protein	unknown	unknown	gnl|CDD|224588
NZ_CP010833.1|WP_079181388.1|35589_36105_-|HAD-hydrolase-like-protein	unknown	unknown	gnl|CDD|319809
NZ_CP010833.1|WP_075262751.1|31246_31690_-|polyketide-cyclase	unknown	unknown	gnl|CDD|176909
NZ_CP010833.1|WP_075262740.1|18404_18584_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262759.1|38032_38416_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262753.1|32433_32655_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_159027389.1|14648_15626_+|hypothetical-protein	unknown	unknown	gnl|CDD|376279
NZ_CP010833.1|WP_075262745.1|24294_24852_+|DNA-binding-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262744.1|22173_24291_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|238045
NZ_CP010833.1|WP_079181386.1|26397_26787_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262741.1|18818_19655_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	gnl|CDD|223713
NZ_CP010833.1|WP_075262749.1|29534_30536_-|aldo/keto-reductase	unknown	unknown	gnl|CDD|381378
NZ_CP010833.1|WP_159027390.1|21948_22110_+|hypothetical-protein	unknown	unknown	gnl|CDD|367510
NZ_CP010833.1|WP_075262755.1|34904_35606_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262750.1|30821_31250_-|SnoaL-like-domain-containing-protein	unknown	unknown	gnl|CDD|226769
NZ_CP010833.1|WP_079181385.1|15694_16423_+|DUF4145-domain-containing-protein	unknown	unknown	gnl|CDD|372658
NZ_CP010833.1|WP_075262754.1|33841_34438_-|hypothetical-protein	unknown	unknown	gnl|CDD|215059
NZ_CP010833.1|WP_075268175.1|16639_16891_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262748.1|29035_29515_-|hypothetical-protein	unknown	unknown	gnl|CDD|379151

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator	csa3	COG0640_csa3_CAS-I-A	1.1e-15	52.7	0.5

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075262739.1|17100_18387_-|hypothetical-protein	gnl|CDD|224588	COG1674, FtsK, DNA segregation ATPase FtsK/SpoIIIE and related proteins [Cell division and chromosome partitioning].	0.000337943
NZ_CP010833.1|WP_159027390.1|21948_22110_+|hypothetical-protein	gnl|CDD|367510	pfam03457, HA, Helicase associated domain. This short domain is found in multiple copies in bacterial helicase proteins. The domain is predicted to contain 3 alpha helices. The function of this domain may be to bind nucleic acid.	0.000106453
NZ_CP010833.1|WP_079181388.1|35589_36105_-|HAD-hydrolase-like-protein	gnl|CDD|319809	cd07506, HAD_like, uncharacterized family of the haloacid dehalogenase-like (HAD) hydrolase superfamily. The haloacid dehalogenase-like (HAD) hydrolases are a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members include 2-L-haloalkanoic acid dehalogenase (C-Cl bond hydrolysis), azetidine hydrolase (C-N bond hydrolysis); phosphonoacetaldehyde hydrolase (C-P bond hydrolysis), phosphoserine phosphatase and phosphomannomutase (CO-P bond hydrolysis), P-type ATPases (PO-P bond hydrolysis) and many others. Members are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	2.29208e-12
NZ_CP010833.1|WP_159027389.1|14648_15626_+|hypothetical-protein	gnl|CDD|376279	pfam18860, AbiJ_NTD3, AbiJ N-terminal domain 3. Alpha + beta domain. Found fused to AbiJ-like HEPN. Fused to other domains presumably involved in defense.	0.00700082
NZ_CP010833.1|WP_075262750.1|30821_31250_-|SnoaL-like-domain-containing-protein	gnl|CDD|226769	COG4319, COG4319, Ketosteroid isomerase homolog [Function unknown].	9.14713e-17
NZ_CP010833.1|WP_075262744.1|22173_24291_+|helix-turn-helix-domain-containing-protein	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	7.28547e-08
NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|223713	COG0640, ArsR, Predicted transcriptional regulators [Transcription].	8.93066e-11
NZ_CP010833.1|WP_075262749.1|29534_30536_-|aldo/keto-reductase	gnl|CDD|381378	cd19152, AKR_AKR15A, AKR15A family of aldo-keto reductase. The AKR15 family includes Microbacterium luteolum pyridoxal 4-dehydrogenase (PLD), Pseudomonas sp. D-threo-aldose 1-dehydrogenase (FDH), and similar proteins. PLD (EC1.1.1.107) catalyzes irreversible oxidation of pyridoxal. FDH(EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose. FDH (EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose.	9.52791e-108
NZ_CP010833.1|WP_075262754.1|33841_34438_-|hypothetical-protein	gnl|CDD|215059	PLN00111, PLN00111, accumulation of photosystem one; Provisional.	0.00394884
NZ_CP010833.1|WP_075262751.1|31246_31690_-|polyketide-cyclase	gnl|CDD|176909	cd08900, SRPBCC_CalC_Aha1-like_7, Putative hydrophobic ligand-binding SRPBCC domain of an uncharacterized subgroup of CalC- and Aha1-like proteins. SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain of a functionally uncharacterized subgroup of CalC- and Aha1-like proteins. This group shows similarity to the SRPBCC domains of Micromonospora echinospora CalC (a protein which confers resistance to enediynes) and human Aha1 (one of several co-chaperones which regulate the dimeric chaperone Hsp90), and belongs to the SRPBCC domain superfamily of proteins that bind hydrophobic ligands. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands.	6.95583e-49
NZ_CP010833.1|WP_079181385.1|15694_16423_+|DUF4145-domain-containing-protein	gnl|CDD|372658	pfam13643, DUF4145, Domain of unknown function (DUF4145). This domain is found in a variety of restriction endonuclease enzymes. The exact function of this domain is uncertain.	1.6799e-10
NZ_CP010833.1|WP_075262748.1|29035_29515_-|hypothetical-protein	gnl|CDD|379151	pfam13378, MR_MLE_C, Enolase C-terminal domain-like. This domain appears at the C-terminus of many of the proteins that carry the MR_MLE_N pfam02746 domain. EC:4.2.1.40.	1.08212e-37

Protein sequences

>NZ_CP010833.1|WP_079181386.1|26397_26787_+|hypothetical-protein
MAYVPQFRRDVLDTAAWLRSGEGSPLPFAGLSAEATHRRLMQRAGDDDEPEADYQLRGRFRVLLWGPTTDNVTAYLFRQEDHLVITLSFWREEHLLSHPEDAGTVFVVEIPAKEFVGILEGIAAALGTS
>NZ_CP010833.1|WP_075262745.1|24294_24852_+|DNA-binding-protein
MGEIEDAIERADRESFTREPPKTLKGQIGYLLKQMGSAKAVAAELGVTADSVNRYRRGARRHARADVAAKIDDAVRQRWQPMVRKRRQKQAAASGGITVETRARFGYTSSAGSTDDGRFRRLTVKLPATYAQRLFDARDTGASDQQMRQIIAEGFKEIYFQDGGGRAAGLSDVTLNDIDYLDVDY
>NZ_CP010833.1|WP_075262744.1|22173_24291_+|helix-turn-helix-domain-containing-protein
MASEEELFASVDALLEEEPQLPPPAERARLREAAGITQARLAVALKTSTQTVKNYENGRSEPKSPRLEAYQRLLKGWAAKYPAHASSAASAPAVAPQPEVPGTFTGSAAPEQAEAATPVQAPAAALAAPERPERSATSRRPAATTAAAPAVDPRFPHGPLAVLDGDGSAYGAGGIVLDCPATTIPELVEWTLRESGLGTAKLNRYGKDSDPLIVLTAAAAVKLGLPERLEGHEQRRSLRLPEDHPVVKQVAKAKWQLTQRGFGPWARIYRKAQGRERQCVQLAILSWDALDERSWPGVSEMEPADIARVLGVYAMRVITPRGSTAVSGLELMTALRPPTKAVRDEETGNWVSGHNAGSLGTEPMDPAPPEATPEHPVVVDSGWKGGFLNEEAYQWVRDVDTLSDEECTLPFAVGLDLNTAFLAAAARLVVGLSAPDHFHAPKFNPKIPGSWLADLSHIELDPRLPSPFTPDGTRPTGAAWYQTHTLAYAQELGHDVHPIEAYLRRETGAYLDPWHDRLKNAYVDTLADMGVTKDLNDVGFLAAMEQHKQNDPALAAVLSAIKATVKGGVGKLRERPQGKSYKEGETWPALSRPTWRPDIRAAVISKARVNMHRKLNNMVKMTGLYPLAVLSDCVVYPSPGESPIDFLPYAASGKPQPGAFRLGPTPGLAKLEGVQSMLWAVDLMEKGLNPARHIKGGDAVMDEGE
>NZ_CP010833.1|WP_159027390.1|21948_22110_+|hypothetical-protein
MTVPRGHVEGVKVGGQEYPVKLGVWIMNQKGRRAKLTPDKLQALAALGLEWAR
>NZ_CP010833.1|WP_075262741.1|18818_19655_+|hypothetical-protein
MTNDFEAHLAATLGAATENIRQTMAASIRPAPKVELPTSLRETLAKAVAPLLPVLERLDAMMPGNWRGQHLDYERMVRLMQEGVPLAWVPPADVIRQLLAADDASSRSKVIDDSHPAILASCREALAEVTDARLTPQRTLLEECARAIENGMFNSAQALAANVWDTLMRGIAFANPDLLTSKGTWNYRHIRRNVPSVDAEEDATLGELRRAAVFLPVAKVLEDFWHPQPVPFGFNRHATAHAAGTVQYTASNAMTALMLAVSVLREIDDQAYVVHIHA
>NZ_CP010833.1|WP_075262740.1|18404_18584_-|hypothetical-protein
MARTKFDKQVDESADTFACGLARMLAGRDLDGVRRTDATFWRSGTRVLPKVEGKVRRRS
>NZ_CP010833.1|WP_075262739.1|17100_18387_-|hypothetical-protein
MSFRLTLCGGLAESGYLTTRDLDATGETLRDLTELWEHREAALAALEPAGIGAASVLTVGTAAYMVLTRERRELMRQWVGPLHEALHQPLGLAEQTDPRRYLHIPKNFSDDDAQIRIDLPTRLGFSRDVVADLITQKLALQGVTFSWHPEGRKPYVLVKKTRKPPAISLFKGPKTRELVAKAKEFAPVIGFGAGGRIVSVDLDAESPHILVNASTGGGKSVILRCIACQMLHHGSRVFVLDTKRISHLWAKALPTVTHRGNIAGIHDALLGLATELERRLDLDGDLDTVPRLIVAIDEANTTLPRLARYWETFRQKDDPKTSPAIAALEQALWFGRAARVHVIFDGRPQATVLRSAARELFATVILARFTTDTWQVLAPDAGPAPKQRHPQQGHFHVIQHGEVDETQAIRMTDADVVAWLTDPDDPTA
>NZ_CP010833.1|WP_075268175.1|16639_16891_-|hypothetical-protein
MRCGSADTRVTRLDPTSAEGTCFRCDKPFHATPCQNCGGFRIDGSFGASGTRFEILPETVRCWDCRHRNPLRDPGPEETASAR
>NZ_CP010833.1|WP_079181385.1|15694_16423_+|DUF4145-domain-containing-protein
MNEQELTSLEQRRAVCPYSDCATGTVMDMVDQRMLAPESREYALAEFGEEGEGALPVYPHSSWTQQECWVCQLCGRSILEVIECKKTGAGREARIEELTRLVLWPSPAPRVLDPDVPERIRSAYEEASRAENAGAARLAGVGYRSAVEELCKDQGATHKTLHGKIRELAAQGLPGDIITALDETRVVGNDSVHQGVAYSAEELADIAELVAEAAVLLYVQPAQRRRMAESRKKRHETAQQNP
>NZ_CP010833.1|WP_159027389.1|14648_15626_+|hypothetical-protein
MNLPSGVPVFKLRDAIAEALWGHVKANRLAAVCEYLGLAPQGADEDPYNSKRGYVLARLEDKSLPDLMDVARRVIKEYGDDDLQQLLAQLGLQGVSGELKNLIFAADGPKPQIVLPDSISNTIRIVKNEQYCLVYDQPLEGRGLSWQDLVTWWVRQHPEHADDPTQARISLRDRLRRSLGDNGAELLVFDTYVKLGFDLPALIPQVYLHYDPYSMSELGGARRLARQRMDFLLLMNHRARAVIEIDGIQHYARPADRAAGQRPDANWLADTGRYASMVAEDRELTLQGYEVYRIGGHELCDAAAPKMLTAFFERLLRRHDHTDSS
>NZ_CP010833.1|WP_075262748.1|29035_29515_-|hypothetical-protein
MAEDPATVDAVRDAGPALRIAVDAHRAYRPAQARKLAAALADRGCWFLEASLVPEDLDGHRRLAGHSPLPLAVGEALRNRYEFAHWLRAGALEIAQPDVTRTGITEAMAIAEISGAHHIPAAPHHSVGLGVALAAGLQVSIRAAHSACESNVMTSFHCF
>NZ_CP010833.1|WP_075262749.1|29534_30536_-|aldo/keto-reductase
MRADDPVSLGRTGLRVSRLGLGLASLGGLFAPVSDTQAAEVLERAWQLGIRLYDTAPVYGYGRSERRTGAALAGRPRDAFVLCTKVGRLIERGGPDTQPIWADPPEEMGPRKDYSFAGVMRSVAESLERLGMDRVDVLHVHDPDEEFGAAVGEAYRALAVLRDRGTIGAVSIGVNHAPVAARFLREAAAPGPDCVLLAGRYGLLDQSGLDELLPLCAERGVAVLAAGVYHGGLLTEPSPGTPHAHTTLPSRTTARIAGWQKLCSRFEVPLLAAAVQLPFGHPAVAAVLVGARTATQVEQSAAWLAHPVPTALWDQARRAGLLPAMCPIPTSCS
>NZ_CP010833.1|WP_075262750.1|30821_31250_-|SnoaL-like-domain-containing-protein
MTPDSERQIRDLLAARTRAFGRRDAATAAADYDDGLVLYDAVGPFVRRGEDQADRLERWIASYRTGIGHEIRDLEITAGTDLAFCHFLVRISGSMRDGTEVGMWVRATCCLRRMDDAWTIVHEHASVPFDADTGQAVLRGEL
>NZ_CP010833.1|WP_075262751.1|31246_31690_-|polyketide-cyclase
MTGHSVKHSTFTLERTYAAPPAAVFAAWSDRDRKAKWFAAGDGRYSLDFRVGGTEAVHGGDGTGLVARSAYHDIVLDERIVYTTALFTGEVLSTVSLTTVRFSPDGERTLLVLTEQGTFLDDQEQPQWREQGTGEWLDALGQEVDER
>NZ_CP010833.1|WP_075262752.1|31686_32031_-|helix-turn-helix-transcriptional-regulator
MLKREVESADRVFHALADPNRRAMIERLTLGPAAVSELAAHLGVTLAATVQHLRVLQDSELVRSEKSGRVRTCRIDTSGLRDAEAWLQHQRTAWEHRLDRLGAVLDDQPKESES
>NZ_CP010833.1|WP_075262753.1|32433_32655_+|hypothetical-protein
MGRPLLPLRSALVPVMAVISGLVAGWLCWIAEGSVPRGDLAGLGAVGLAAPFFNRLLAAEAAERTGEEVRGRG
>NZ_CP010833.1|WP_075262754.1|33841_34438_-|hypothetical-protein
MRIATASAAATFCAAALALTFGTAVAVTPADGAPAEQAGGQPACGSVESYRLGAPYSGNINRNGNEMPVHLTPGAEQHRIGRISTGPVTGPATTPDGKTFTIENEWTALDDMITKAVANYQVRDADGVEVGKVTCDPATGAVTGVVAHDIDATFGGHELQTCESSICSGGSGAHSWTPERIDRHIVGTLTLTSDQAAN
>NZ_CP010833.1|WP_075262755.1|34904_35606_+|hypothetical-protein
MRFPRFNEDGPLVGYELEAMRSLSSAFLTARYEWQAACTMWDRLYTAGETAELRRSPASFSFYEEAVGRLAGGVRDYERQAALVAWRYTAASLVLGVTVLRRIAEGKPPLTVTGVEELCQEPALGQLHEALSVPVPDLVPERRHPADIPGDRECSAREWGTVREGVADVIDLVLELAIDEDAAHPRTRDEAATCLLTQHCPPHTEPVHDGVLQPLFQLAEQVPYGIARIIDHG
>NZ_CP010833.1|WP_079181388.1|35589_36105_-|HAD-hydrolase-like-protein
MRAGDADAGAATGHLIEYVNVPIGGYTSDSPHRPNLVGISQSRAVERHGKMFGSSNTVIIGDSLQDVTTGIEAGAKVIGVTSGTTSAQQLADAGAHLVIPGLRNSESLLSLIRSLSSQWHLAGAGPVAPTLPSSPFRLGFDALVSAPAERSRGVRHRAPSQTATRCFNRGR
>NZ_CP010833.1|WP_075262759.1|38032_38416_-|hypothetical-protein
MGLVLFPGDGDNSSPDVSWSYSGFAAFRQRLAEAEGFALSEMWGFGGERPWSEVSTALEPLLDHPDAGGDDLSPTECASVLIRLEAITDQWARKSGDQLHQQHIEDARQLAGILRLCIEKDVPLVFL

Crispr_ID: NZ_CP010833_3

• CRISPR_ID: NZ_CP010833_3
• CRISPR_location: 157998-158088
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_3

Consensus_repeat	Method
GGTGCGTCACGGGCCGTGCGTCGTCGCGCGTCA	CRISPRCasFinder

spacers of NZ_CP010833_3

>3.1|158031|25|NZ_CP010833|CRISPRCasFinder
CGGGCCGTGGTGCGTCACGGGCCGT

CRISPR arrays and Neighbor proteins around NZ_CP010833_3

CRISPR arrays

The CRISPR arrays of NZ_CP010833_3

>merge|NZ_CP010833|3|157998-158088|CRISPRCasFinder
GGTGCGTCACGGGCCGTGCGTCGTCGCGCGTCACGGGCCGTGGTGCGTCACGGGCCGTGGTGCGTCACGGGCCGTGCGTCGTCGCGCGTCA

>NZ_CP010833|3|3|157998-158088|CRISPRCasFinder
GGTGCGTCACGGGCCGTGCGTCGTCGCGCGTCA	CGGGCCGTGGTGCGTCACGGGCCGT
GGTGCGTCACGGGCCGTGCGTCGTCGCGCGTCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_029182475.1|168823_169003_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262849.1|169094_169529_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075262847.1|166976_167864_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224048
NZ_CP010833.1|WP_075262837.1|147839_148964_-|DeoR/GlpR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|380483
NZ_CP010833.1|WP_075262848.1|167898_168399_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_CP010833.1|WP_075262845.1|162638_164168_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|173861
NZ_CP010833.1|WP_075262838.1|149339_151754_+|polysaccharide-lyase-8-family-protein	unknown	unknown	gnl|CDD|238517
NZ_CP010833.1|WP_075268187.1|145178_145982_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP010833.1|WP_075262839.1|151764_152619_-|aminoglycoside-3-N-acetyltransferase	unknown	unknown	gnl|CDD|376807
NZ_CP010833.1|WP_079181591.1|161643_162387_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_075262850.1|169699_170674_-|sporulation-protein	unknown	unknown	gnl|CDD|369195
NZ_CP010833.1|WP_075262843.1|157268_157895_+|TetR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|274678
NZ_CP010833.1|WP_075262842.1|155965_157258_+|family-1-glycosylhydrolase	unknown	unknown	gnl|CDD|274539
NZ_CP010833.1|WP_107472854.1|152729_153242_+|DinB-family-protein	unknown	unknown	gnl|CDD|368218
NZ_CP010833.1|WP_075262841.1|154047_155685_-|family-20-glycosylhydrolase	unknown	unknown	gnl|CDD|119336
NZ_CP010833.1|WP_079181395.1|165144_166980_+|dipeptide/oligopeptide/nickel-ABC-transporter-permease/ATP-binding-protein	unknown	unknown	gnl|CDD|223521
NZ_CP010833.1|WP_075262846.1|164206_165148_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|223674
NZ_CP010833.1|WP_079181394.1|160739_161654_+|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl|CDD|238861
NZ_CP010833.1|WP_075262836.1|146281_147586_-|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270303
NZ_CP010833.1|WP_075262840.1|153343_154108_+|transporter-substrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|270341

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075262850.1|169699_170674_-|sporulation-protein	gnl|CDD|369195	pfam07070, Spo0M, SpoOM protein. This family consists of several bacterial SpoOM proteins which are thought to control sporulation in Bacillus subtilis.Spo0M exerts certain negative effects on sporulation and its gene expression is controlled by sigmaH.	5.90264e-97
NZ_CP010833.1|WP_075262847.1|166976_167864_+|ABC-transporter-ATP-binding-protein	gnl|CDD|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	1.49591e-110
NZ_CP010833.1|WP_075262837.1|147839_148964_-|DeoR/GlpR-family-transcriptional-regulator	gnl|CDD|380483	cd01541, PBP1_AraR, ligand-binding domain of DNA transcription repressor specific for arabinose (AraR) which is a member of the LacI-GalR family of bacterial transcription regulators. Ligand-binding domain of DNA transcription repressor specific for arabinose (AraR) which is a member of the LacI-GalR family of bacterial transcription regulators. The ligand-binding domain of AraR is structurally homologous to the periplasmic sugar-binding domain of ABC-type transporters and both domains contain the type 1 periplasmic binding protein-like fold. The LacI-GalR family repressors are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the type 1 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	1.08874e-45
NZ_CP010833.1|WP_075262848.1|167898_168399_-|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	8.5785e-27
NZ_CP010833.1|WP_075262845.1|162638_164168_+|ABC-transporter-substrate-binding-protein	gnl|CDD|173861	cd08496, PBP2_NikA_DppA_OppA_like_9, The substrate-binding component of an uncharacterized ABC-type nickel/dipeptide/oligopeptide-like import system contains the type 2 periplasmic binding fold. This CD represents the substrate-binding domain of an uncharacterized ATP-binding cassette (ABC) type nickel/dipeptide/oligopeptide-like transporter. The oligopeptide-binding protein OppA and the dipeptide-binding protein DppA show significant sequence similarity to NikA, the initial nickel receptor. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA can bind peptides of a wide range of lengths (2-35 amino-acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	7.47061e-143
NZ_CP010833.1|WP_075262838.1|149339_151754_+|polysaccharide-lyase-8-family-protein	gnl|CDD|238517	cd01083, GAG_Lyase, Glycosaminoglycan (GAG) polysaccharide lyase family. This family consists of a group of secreted bacterial lyase enzymes capable of acting on glycosaminoglycans, such as hyaluronan and chondroitin, in the extracellular matrix of host tissues, contributing to the invasive capacity of the pathogen. These are broad-specificity glycosaminoglycan lyases which recognize uronyl residues in polysaccharides and cleave their glycosidic bonds via a beta-elimination reaction to form a double bond between C-4 and C-5 of the non-reducing terminal uronyl residues of released products. Substrates include chondroitin, chondroitin 4-sulfate, chondroitin 6-sulfate, and hyaluronic acid. Family members include chondroitin AC lyase, chondroitin abc lyase, xanthan lyase, and hyalurate lyase.	0
NZ_CP010833.1|WP_075268187.1|145178_145982_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.33555e-51
NZ_CP010833.1|WP_075262839.1|151764_152619_-|aminoglycoside-3-N-acetyltransferase	gnl|CDD|376807	pfam02522, Antibiotic_NAT, Aminoglycoside 3-N-acetyltransferase. This family consists of bacterial aminoglycoside 3-N-acetyltransferases EC:2.3.1.81, these catalyze the reaction: Acetyl-Co + a 2-deoxystreptamine antibiotic <=> CoA + N3'-acetyl-2-deoxystreptamine antibiotic. The enzyme can use a range of antibiotics with 2-deoxystreptamine rings as acceptor for its acetyltransferase activity, this inactivates and confers resistance to gentamicin, kanamycin, tobramycin, neomycin and apramycin amongst others.	6.56178e-93
NZ_CP010833.1|WP_079181591.1|161643_162387_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	3.74163e-14
NZ_CP010833.1|WP_075262843.1|157268_157895_+|TetR-family-transcriptional-regulator	gnl|CDD|274678	TIGR03613, RutR, pyrimidine utilization regulatory protein R. This protein is observed in operons extremely similar to that characterized in E. coli K-12 responsible for the import and catabolism of pyrimidines, primarily uracil. This protein is a member of the TetR family of transcriptional regulators defined by the N-teminal model pfam00440 and the C-terminal model pfam08362 (YcdC-like protein, C-terminal region).	6.5328e-11
NZ_CP010833.1|WP_075262842.1|155965_157258_+|family-1-glycosylhydrolase	gnl|CDD|274539	TIGR03356, BGL, beta-galactosidase.	2.59893e-79
NZ_CP010833.1|WP_107472854.1|152729_153242_+|DinB-family-protein	gnl|CDD|368218	pfam04978, DUF664, Protein of unknown function (DUF664). This family is commonly found in Streptomyces coelicolor and is of unknown function. These proteins contain several conserved histidines at their N-terminus that may form a metal binding site.	7.12197e-40
NZ_CP010833.1|WP_075262841.1|154047_155685_-|family-20-glycosylhydrolase	gnl|CDD|119336	cd06568, GH20_SpHex_like, A subgroup of the Glycosyl hydrolase family 20 (GH20) catalytic domain found in proteins similar to the N-acetylhexosaminidase from Streptomyces plicatus (SpHex). SpHex catalyzes the hydrolysis of N-acetyl-beta-hexosaminides. An Asp residue within the active site plays a critical role in substrate-assisted catalysis by orienting the 2-acetamido group and stabilizing the transition state. The GH20 hexosaminidases are thought to act via a catalytic mechanism in which the catalytic nucleophile is not provided by solvent or the enzyme, but by the substrate itself. Proteins belonging to this subgroup lack the C-terminal PKD (polycystic kidney disease I)-like domain found in the chitobiases.	1.78457e-122
NZ_CP010833.1|WP_079181395.1|165144_166980_+|dipeptide/oligopeptide/nickel-ABC-transporter-permease/ATP-binding-protein	gnl|CDD|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.17402e-121
NZ_CP010833.1|WP_075262846.1|164206_165148_+|ABC-transporter-permease	gnl|CDD|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.20734e-95
NZ_CP010833.1|WP_079181394.1|160739_161654_+|SGNH/GDSL-hydrolase-family-protein	gnl|CDD|238861	cd01823, SEST_like, SEST_like. A family of secreted SGNH-hydrolases similar to Streptomyces scabies esterase (SEST), a causal agent of the potato scab disease, which hydrolyzes a specific ester bond in suberin, a plant lipid. The tertiary fold of this enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles two of the three components of typical Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxylic acid.	5.63846e-63
NZ_CP010833.1|WP_075262836.1|146281_147586_-|sugar-ABC-transporter-substrate-binding-protein	gnl|CDD|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.71624e-71
NZ_CP010833.1|WP_075262840.1|153343_154108_+|transporter-substrate-binding-domain-containing-protein	gnl|CDD|270341	cd13623, PBP2_AA_hypothetical, Substrate-binding domain of putative amino-acid transport system; the type 2 periplasmic binding protein fold. This putative amino acid-binding protein belongs to the type 2 periplasmic-binding fold protein (PBP2) superfamily, whose members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. PBP2 typically comprises of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two receptor cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	1.39104e-85

Protein sequences

>NZ_CP010833.1|WP_075262843.1|157268_157895_+|TetR-family-transcriptional-regulator
MAKRGPYEKGEAKRTEILHAALEIFAAEGYRGTSLRKVAAKCSLSLPGLMHYFSSKEDLLTQVLRMRDETARARQNERTDPESYREIIREGARTPGLVELFVSMAAAAGDPEHPAHAHFAERYPVLRERVARYVQQRMDDGRITTLIPAERLAVLLLAVADGIQLQWLIDRSTNMEQPIDDIMRLLALDQEGARNDEGQGGTADRAED
>NZ_CP010833.1|WP_075262842.1|155965_157258_+|family-1-glycosylhydrolase
MTPPTGPRLALPEGFLMGASTSAHQVEGNNVGSDWWAAENRPGSFVAERSGDAADSFHRWPEDMDLLHELGFNAYRFSIEWARIEPERGHVSRAAVAHYRAMVRGALDRGLTPVVTLHHFTSPKWFSALGGWASPEAPALFAGYAEVATEILAAGARYVATINEPNMIALMHTVIRRLGSGGEAGGTEDGEEAGAGAFDASGVEPDAEVTRSLIRAHRAAYDVLKAADPGLRVGWTVANQVYQPEPGATEVAEAHAYPREDVFLEAAREDDWIGVQAYTRHRIGPDGPLPVEPGTETTLTGWEFYPEALGLAIRHTVAVVGPHVPVLVTENGIATDDDERRIAYTTGALASLASALRDGIDVRGYLHWSALDNYEWGSYRPTFGLIAVDPRTFARTPKPSARWLGALARAAHIPDGRPAAGVPAGAHSAG
>NZ_CP010833.1|WP_075262841.1|154047_155685_-|family-20-glycosylhydrolase
MNAVIPQPRQAIRTASTAGPRTTGAWQVHSADARLMGLAATVHALLAPHLGDRLQPLGASPDPGAATLTLALGDAAAADFPAPVGIAPTGEAEPVDESYRLTVGPRGIACRAATPAGVFRAATTALQLLGASGDRIPCQELTDAPHFAWRGLLVDPARGYLAPGELRSLIDLAALYKLNVLHLHLTDNEGWRLEIPGVPELTAPAPDGTPRAFYTADDYRELQAYAAERFVTLVPEIDLPGHCATLREALPGLPDAPAPEGLTGRFPFVPPLDLADPATAKAVATILDDVCRLTDGPFVHIGGDEAVGATEDSFVGSIRELRSLVRGFGKRPVGWQESSRAGIGPEDIAQFWVDVPMMDLPDTAEELAARPELLAAGQTVEFIAALKAFFAPADQDLARILDGGGRVLLSPQSHLYLDRAYAPQVVPSGQASAAARLGFPTYRPLGVEHAARWDPASHNIPDDRIAGVEATVFAESITSLDDVTTLLLPRLPSVAAAAWSGRAPDWNDHRIRLAHHGRLWEQRGLAYLASTEISWAGATDAPSTP
>NZ_CP010833.1|WP_075262840.1|153343_154108_+|transporter-substrate-binding-domain-containing-protein
MTQQPTPSALVSAFAPDGALRASINLGNPILAHRDPASGEPAGVSVDLAREFGRRLGVPVELVAFERATLSVDAVRAERADIGFFAVDPARSEGLRFTAPYVLIEGSYLVPERATIAENGQVDREGTRISVGAGSAYDLFLTREIRHAEVVRLEGAPRALAALRAGEVEVAAGIRQLLEAEAAREAGVRVLPGRFMVIQQAMGVPAGRGAAAQELLASFVEEMKADGFVADALERHGVEGASVAPAQEISVDAR
>NZ_CP010833.1|WP_107472854.1|152729_153242_+|DinB-family-protein
MMRDDRVGPPLLGGERETLRAFLDYHRGTLAMKCAGLSDEQLRERSMEPSTLSLLALLRHMAEVERAWFRRVFEDEAAPMVWSEKPFDFQAAYDASASTGAEAFAAWEAEVETSRRIERKAASLDLVGRQPRWEKDVSLRMVMVHVLLEYGRHNGHADLLREGVDGTVGA
>NZ_CP010833.1|WP_075262839.1|151764_152619_-|aminoglycoside-3-N-acetyltransferase
MDVRELLRRSGGPVTRDRIGDDLAALGLGPGDTVMFHTRLSAIGYVPGGPQTVIDALLDVVGPTGTLMVSCGWNDAPPYDFTTWPGAWQDAVRAHHPAYDPALSEADHNNGRLPEALRRRPGAVRSRHPDASLAALGPSAAALMADHPWDDPHGPGSPLARLVALGGRVLLLGAPGETMTLLHLAESLARAPGKRFVTYEQPVRVDGVREWRTFHDIDSTDGAFDYSRVVPEGQDPFAVIVRAMLDAGIGRTGTVGAADSRLFDAGPAVDFGVRWIEEQLNAPG
>NZ_CP010833.1|WP_075262838.1|149339_151754_+|polysaccharide-lyase-8-family-protein
MTSAWSRRTFLATSAVLTAAGGGALMLAAPGAASAAPEDDPYAALRTTWSALILGEGFSPTAEPFKSRLADLGAKASQWLDTMAPAEGSLWPDAVFADPDPDTDPESYVFSGRMADSFIRLNTMAQAYRQQGTGLTGNTALSDAVLTGLEHLNTQVYNDGQTRYGNWYSWQIGAPQALLDVCVLMYDAIAPEARARYCAAVDHFVPDSAVASYTGTSTGANRVDLCRVLALRGVVGGTAAKIALARDALSPVFPLVTKGDGLYADGSFIQHTTVPYTGSYGSVMLGGLGLLFALLKGTTWEVTDPNRQVVFDAVENAWAPFLYNGLVMDSVAGRAISRGEVDDHRRGHPIMASIVLLGQGASAAENARWRALVKGWAQRDYYSPPLSNPSLGLTALARIKSVLDDTSLTRVAEPTGHRLFPDMARATHRRPGWAASLSMADRRITFYETGNGENLRGWHTGNGMLYWWGDTFANGQYSDAFWPTVDPYRLPGTTVSRKALADGAGGDWGVALPDVNWVGGVTDRKRAAVGQYLKGLTSTLMAKKSWFFLDDTVVCLGAGIHGRDGAAVETTVDNRNLGPTGNAPFTVDGSAKPVAAPWSATLSGASWAHLAGHGGYVFPGGATVKALRENRTGRWRDINRAGSTDPVSRKYLTLWFDHGTDPSGATYAYQLLPGASEQRTAARAADSGWLRVLANTDDQQGVAVPSLGLTAVNFWFGGSVGPLVADAPCSVMVTEHGDGTATVLVSDPMRARTSLTLTWNRAVASVVSMPATVTSATTGGSLRLVFGDLSGTRGATQTVKVRLA
>NZ_CP010833.1|WP_075262837.1|147839_148964_-|DeoR/GlpR-family-transcriptional-regulator
MRLHVDQRHERVLELVRERGSLRVAELAEELGMSAVTLRRDVEALAAQGLVERLHGAVVWPSGQSRSAPAPAPSAEGLVVGMVVPTTEYYYADVVRGARETVEAAGARLTIGLSRYLPDEDAAQARRLLSTGADGLLLTPSWERGCPEQGEGLWTVEQKTPVVLVERSAPLGHPAARLDRVRSDHAHGAAEAVAHLAGLGHRAIALAVQDSPTAPRLRVGYRAAVEALGLTPVSPSPLDEAPSRSEADRFERTLEYLCQGVASGYVTAAIVHSDADAIVLIPRLQARGVRVPEDLAVIAYDDEVASLADLPLTAVAPDKHAVGAAAARLLLARLGVDDPGATDTTGPGAGARRHLDILPTLRVRVSCGAAAAAS
>NZ_CP010833.1|WP_075262836.1|146281_147586_-|sugar-ABC-transporter-substrate-binding-protein
MPCIARTSRLALVASAASLALLVTACGGSGSDASGPGDGKPVTLTFWSATAGAKETADAFNKTHTDIKVKFSMVPAGPEGVTKLSNAVKGGNAPDVATMDYSALPEYASEGNLENLTPSSGDLVKKEFPEAVQSLVNLGGSTWAVPFDVTPIQLFYRKDLFKKHGVDVPTTWAEYRTAAEKIHAGDPDVTITNFGGGDPALLSGLAWQAGARWYGTSGDAWKVNIDDPASRKVAAYWDDLLADGLASKTPLWGEGENKERATGKVATIIGAAWSAGNFPVSYPDAKGKWGIAPLPTWDGKASTGMYGGTSYIVPKGSEHTEAAAEFIKWVTTDPAAMTARLSSLKAPSSALPANEGMRAAAAKEFDSSYFGDQDVYALAGEAAGTIVPGWTWGPVQQQVTSVQMAAGGDHTKMLSTGQAKGESAVTDRGLKLDK
>NZ_CP010833.1|WP_075268187.1|145178_145982_-|sugar-ABC-transporter-permease
MVYAAWMSLYREESSGLGFGGTERVFAGFGNFTEALGNEAFLRSFGNIALYCALYIPAMVGGALVLALLVDSAMARARRFFQIAYFLPHAVPGLIASLIWLYLYTPGLSPVTDALDAVGAHWNFFGESEAIFSVVNISAWQWTGYNMIIFYAGLQAVPREVLEAATVDGAGALRTALQVKIPMIRPTVVLTLLFTCVGAIQLFDAPKLVQLRANTMGEDWSPTMFIYTVAFKGHDYGLAAASSLLLALVAGLLSFVVTKLGNRWKAS
>NZ_CP010833.1|WP_079181394.1|160739_161654_+|SGNH/GDSL-hydrolase-family-protein
MPFPIRRSAPVASRHLPTTTTLAVASATALLAGTAATASAAPASVRTDDAAPLHYVALGDSFSSGPGIPDQTDEACGRSSRNYPTLVAASLGAASFTDVTCAGADTRHMTTPQGAANPQFDALRPDTTLVTLGIGGNDLDLAGVLTRCVLLGKLAPLGAPCKRSYTLLGTDEIGSRIDATAPRVAAALDEIHGRSPQARVLVVGYPAIVPDDGTACRATVPLAEGDFAWFRDKQKQLNSMLAREAGNGRDTYVDAYAPSIGHDACKPRGVRWIEPEQTAEAAGFHPNAAGHRSTADAALATLTH
>NZ_CP010833.1|WP_079181591.1|161643_162387_-|TetR/AcrR-family-transcriptional-regulator
MHLPSEADTHRPSETGTHRPAKGDVHRPSKGERTRARILGSATELFSRSGFHAVSLRDIAAHAGLTHAGLLHHFPGKESLLIEVLERRDRIDARELFPGVARPGAPVPPPAERLRLLIGVVARNTRTPGLVALYAKLSAEATDPAHPAHRYFTRRYRLLRAELSDLVRALQDEAGRPGDLDPAVVAGQLLALMDGLQTQWLLEPGAVPMEELVCDFLDRLGLLPADGPEGTDRPEEADGAGAAGVSG
>NZ_CP010833.1|WP_075262845.1|162638_164168_+|ABC-transporter-substrate-binding-protein
MSRTTRSGALAACLATVLTLAGCADTGARGGAGTQLSIATLSYPQSLDPAQAVGSALPFFQAAYDTLLKREPDGSFSPMLATKWTYNDKGTELALTLREDVKFADGTAFDAAAVKANLERFKKGGGADAKWLDGLASVKVVDSSHVTLKLAGPDPAMLFYLSDAAGLMANPTAFAKGDSLKTTPDGTGPYRLVKARTTIGTKWVYERNTGYWGEELPYKDLSISFFDNETAIVNGIRTGQVNAALLQNADQQISVESDPRVKTTEQEFDFQGLLLFDRDGKLTPALKDPRVRQALNHAVDRKTMLATIRQNRGATTAQVFGPDTEGYDAKLDTHYAHDPAKAEALLKAAGYAKGFTLKLPRITAIVNDALAASLATDFKAVGVTLKWDDLDGGSAVQKVFTDRAYSGMVMNMGQAASDWIVVNELVTPGAFNMFGTTDATVQKLVPRIRGGSGDDAKQAAKDLNRHLVENGWFLPFYRMSYLHVSDGTVEITPQSGMAVPSIYNYAPTG
>NZ_CP010833.1|WP_075262846.1|164206_165148_+|ABC-transporter-permease
MLNFIARRIAAGALLLLVISLLSYLLLSIPALDVGRQLLGQGADQAAVDAKNASLGLDRPVLVQYGDWLAHAVRGDLGTSWFTSEDVATTVSARLPVTASLMVGVTLVATVVSFLLGVWAGVRRGVVDRFVQVLGVVGYALPGFLVTLVIVLVFAVNLNWFPAIGYTPFAASPSGWLSTITLPVLSLSVASVAGVSQQVRGAVIDVLRQDYVRTLRARGLPMSRIVFRHVLRNASAPALSVLGMQFVGLLGGAVLVEQIFGLPGIGSMTVTYTTRGDIPVIMALVMLTVIGVVLINLLVDVMIGWLNPKARVA
>NZ_CP010833.1|WP_079181395.1|165144_166980_+|dipeptide/oligopeptide/nickel-ABC-transporter-permease/ATP-binding-protein
MSGNLPTGAAAPPRTAHEAEAEAGSGSGAAAPGRGGAVRRLLRNPLGAASAAVLLLLLVAVLLAPLLAPQAPDVSSLGDAFAGPDAAHPLGMDSAGRDILSRILYGGRNTLGGALIALAVALALGVPAGLYAGYYGGRFDSVAGWGVNLVMALPAMVVLLASRAILGPNVWVLMIVLGVLAAPSFFRLVRGIVAGVRKELYVDAARVSGLSDTRIVVRHILIVVRGPVIIQVALVAGVAIGLQAGLEFLGVGSGSSATWGAMLNEAFQNIQRAPLLMLWPGLALGLTNGALVLLAGALRDVLEERGGPDGGRAAHRTQKEPTPPAAPTESGARSPLLSVRGLTVVYGKPDGTRKQVVHGVDLDVHPGEIVGLVGESGSGKTQTAFSVLGILPEGGRIGEGSITVGGREVAGLPERAHRALRGGTVAYVPQEPMSNLDPAFTIGSQLVEPIRHVLGLSRQEAAARALDLLRLVEIPDPERTMRLYPHEISGGMAQRVLIAGAMSCDPELLIADEPTTALDVLVQAEILNLLRRLQQDRGLGVLLVTHNLGVVADLCDRVAVMSEGRIVETGTAEHIVHSPGHPYTRSLLGAVLDDAPAREPWQPREARSTTV
>NZ_CP010833.1|WP_075262847.1|166976_167864_+|ABC-transporter-ATP-binding-protein
MTSTADRDAPAEASDGLPDALLRVRDLRVSYPGRGRRAPRAEILKGVCLDIRPGETLGLVGESGSGKTTIGRAVLGLAPVQSGSITFAGERIERAGAARRRALSRDLQVVFQDPYTSLNPSRTVGDTLGEPLLGQGVGAKEARARITELLDRVRLPADAADRLPREFSGGQRQRVAIARALALRPRLVICDEPVSALDLTTQRTVLELLLEIQEESGVAYLFVTHDLSVVRFMSHRVAVIRGGELVETGDARSVTSEPRHPYTRALMLAAPVADVMEQRRRREAVQATAQASAPS
>NZ_CP010833.1|WP_075262848.1|167898_168399_-|GNAT-family-N-acetyltransferase
MTPTLRTERLLLEPYAPEDEEDFVALFQDTRVSRWMGDGPSSEAEDRALFGRIFTKVYAQNLFAVWAVRRDGRLVGHAEIKRTDTVDGHEIIYALAPAAWGSGLGTELARAVVVHGFDTLGLDEVHATVAAANEASLTLLDRMGFVYVRDIEEEDGSTTRVLTLRR
>NZ_CP010833.1|WP_029182475.1|168823_169003_-|hypothetical-protein
MLGIAAAVLFFIAFLINAADISTNDVFASTNVMLLGLMLLALHVAGVGAGTRIGGSRRR
>NZ_CP010833.1|WP_075262849.1|169094_169529_-|hypothetical-protein
MNPGTPPPDPRHRRPEGVTDTTVEALGALSKALETAERARGALYDFHQLTGSADLALDDAVRLLRAAGHGHRADQVEREILGRNVIPGHWTFQIVEEYNDTYYDVFRAVEREIRQELAEGRDHLHEAGMKAARRTQGHPDHTAD
>NZ_CP010833.1|WP_075262850.1|169699_170674_-|sporulation-protein
MVFKKLLGALGVGGPSVDTVLQPGPALPGGLLSGEVRLRGGGSDVTVDRISLLLVARVEREGQEEEDEATVVLERFTVGGGFRLAEEADHTVPFTVTLPWETPITELHGQHLGPVLGIRTELEIAGARDKGDLDALAVGPLPAQEAILEAFGQLGYAFRSADLELGHIRGTGQQLPCYQEIEILPPAGHAHTVNEIEVTFIAAPGGLEIVIEADKRAGLFSEGHDTVHRFTASHHAAPQTDWNAQVDAWLKEVIAGHESHGAPSSYGDEHGDRHRSGPGAGAVVAGVAAGVAVGVVGGMVAAEVVDEIGDAFEGEEDEEGEDEG

Crispr_ID: NZ_CP010833_4

• CRISPR_ID: NZ_CP010833_4
• CRISPR_location: 840009-840090
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_4

Consensus_repeat	Method
CAGGGATGACGGGACAGCCCTTAG	CRISPRCasFinder

spacers of NZ_CP010833_4

>4.1|840033|34|NZ_CP010833|CRISPRCasFinder
GTCCTGTCGTCAAACTGCCGTCGTCGCCCGAATA

CRISPR arrays and Neighbor proteins around NZ_CP010833_4

CRISPR arrays

The CRISPR arrays of NZ_CP010833_4

>merge|NZ_CP010833|4|840009-840090|CRISPRCasFinder
CAGGGATGACGGGACAGCCCTTAGGTCCTGTCGTCAAACTGCCGTCGTCGCCCGAATACAGGGATTACGGGACAGCCCTTAG

>NZ_CP010833|4|4|840009-840090|CRISPRCasFinder
CAGGGATGACGGGACAGCCCTTAG	GTCCTGTCGTCAAACTGCCGTCGTCGCCCGAATA
CAGGGATTACGGGACAGCCCTTAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075263289.1|829760_831272_-|hypothetical-protein	unknown	unknown	gnl|CDD|237057
NZ_CP010833.1|WP_075263304.1|846604_847951_-|6-phospho-beta-glucosidase	unknown	unknown	gnl|CDD|133432
NZ_CP010833.1|WP_010058123.1|835666_835930_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_093812656.1|837816_838353_+|excalibur-calcium-binding-domain-containing-protein	unknown	unknown	gnl|CDD|377566
NZ_CP010833.1|WP_075263302.1|845617_846094_+|ATP-binding-protein	unknown	unknown	gnl|CDD|340413
NZ_CP010833.1|WP_075263294.1|836480_837695_+|acyl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173847
NZ_CP010833.1|WP_075263290.1|831624_832281_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_010058136.1|844313_844550_-|DUF397-domain-containing-protein	unknown	unknown	gnl|CDD|377231
NZ_CP010833.1|WP_075263296.1|839007_839868_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075263298.1|842272_842860_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_CP010833.1|WP_075263293.1|836002_836476_+|SCP2-sterol-binding-domain-containing-protein	unknown	unknown	gnl|CDD|376720
NZ_CP010833.1|WP_075263305.1|848074_849655_-|cytochrome-P450	unknown	unknown	gnl|CDD|225035
NZ_CP010833.1|WP_075263303.1|846087_846525_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_159024699.1|838701_838878_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075263299.1|842922_843357_-|hypothetical-protein	unknown	unknown	gnl|CDD|225557
NZ_CP010833.1|WP_075263297.1|840156_842247_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075263300.1|843456_844266_-|SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|252734
NZ_CP010833.1|WP_075263301.1|844549_845410_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379262
NZ_CP010833.1|WP_075263291.1|832506_833442_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075263292.1|834250_835465_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379258

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075263289.1|829760_831272_-|hypothetical-protein	gnl|CDD|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	2.51765e-05
NZ_CP010833.1|WP_075263304.1|846604_847951_-|6-phospho-beta-glucosidase	gnl|CDD|133432	cd05296, GH4_P_beta_glucosidase, Glycoside Hydrolases Family 4; Phospho-beta-glucosidase. Some bacteria simultaneously translocate and phosphorylate disaccharides via the phosphoenolpyruvate-dependent phosphotransferase system (PEP-PTS). After translocation, these phospho-disaccharides may be hydrolyzed by the GH4 glycoside hydrolases such as the phospho-beta-glucosidases. Other organisms (such as archaea and Thermotoga maritima ) lack the PEP-PTS system, but have several enzymes normally associated with the PEP-PTS operon. The 6-phospho-beta-glucosidase from Thermotoga maritima hydrolylzes cellobiose 6-phosphate (6P) into glucose-6P and glucose, in an NAD+ and Mn2+ dependent fashion. The Escherichia coli 6-phospho-beta-glucosidase (also called celF) hydrolyzes a variety of phospho-beta-glucosides including cellobiose-6P, salicin-6P, arbutin-6P, and gentobiose-6P. Phospho-beta-glucosidases are part of the NAD(P)-binding Rossmann fold superfamily, which includes a wide variety of protein families including the NAD(P)-binding domains of alcohol dehydrogenases, tyrosine-dependent oxidoreductases, glyceraldehyde-3-phosphate dehydrogenases, formate/glycerate dehydrogenases, siroheme synthases, 6-phosphogluconate dehydrogenases, aminoacid dehydrogenases, repressor rex, and NAD-binding potassium channel domains, among others.	0
NZ_CP010833.1|WP_093812656.1|837816_838353_+|excalibur-calcium-binding-domain-containing-protein	gnl|CDD|377566	pfam05901, Excalibur, Excalibur calcium-binding domain. Extracellular Ca2+-dependent nuclease YokF from Bacillus subtilis and several other surface-exposed proteins from diverse bacteria are encoded in the genomes in two paralogous forms that differ by a ~45 amino acid fragment, which comprises a novel conserved domain. Sequence analysis of this domain revealed a conserved DxDxDGxxCE motif, which is strikingly similar to the Ca2+-binding loop of the calmodulin-like EF-hand domains, suggesting an evolutionary relationship between them. Functions of many of the other proteins in which the novel domain, named Excalibur (extracellular calcium-binding region), is found, as well as a structural model of its conserved motif are consistent with the notion that the Excalibur domain binds calcium. This domain is but one more example of the diversity of structural contexts surrounding the EF-hand-like calcium-binding loop in bacteria. This loop is thus more widespread than hitherto recognized and the evolution of EF-hand-like domains is probably more complex than previously appreciated.	1.54447e-17
NZ_CP010833.1|WP_075263302.1|845617_846094_+|ATP-binding-protein	gnl|CDD|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	2.00611e-16
NZ_CP010833.1|WP_010058136.1|844313_844550_-|DUF397-domain-containing-protein	gnl|CDD|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	9.45906e-18
NZ_CP010833.1|WP_075263294.1|836480_837695_+|acyl-CoA-dehydrogenase	gnl|CDD|173847	cd01158, SCAD_SBCAD, Short chain acyl-CoA dehydrogenases and eukaryotic short/branched chain acyl-CoA dehydrogenases. Short chain acyl-CoA dehydrogenase (SCAD). SCAD is a mitochondrial beta-oxidation enzyme. It catalyzes the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of SCAD is reoxidized in the oxidative half-reaction by electron-transferring flavoprotein (ETF), from which the electrons are transferred to the mitochondrial respiratory chain coupled with ATP synthesis. This subgroup also contains the eukaryotic short/branched chain acyl-CoA dehydrogenase(SBCAD), the bacterial butyryl-CoA dehydorgenase(BCAD) and 2-methylbutyryl-CoA dehydrogenase, which is involved in isoleucine catabolism. These enzymes are homotetramers.	1.02239e-120
NZ_CP010833.1|WP_075263301.1|844549_845410_-|helix-turn-helix-domain-containing-protein	gnl|CDD|379262	pfam13560, HTH_31, Helix-turn-helix domain. This domain is a helix-turn-helix domain that probably binds to DNA.	3.84603e-09
NZ_CP010833.1|WP_075263293.1|836002_836476_+|SCP2-sterol-binding-domain-containing-protein	gnl|CDD|376720	pfam02036, SCP2, SCP-2 sterol transfer family. This domain is involved in binding sterols. It is found in the SCP2 protein, as well as the C-terminus of the enzyme estradiol 17 beta-dehydrogenase EC:1.1.1.62. The UNC-24 protein contains an SPFH domain pfam01145.	1.48731e-09
NZ_CP010833.1|WP_075263305.1|848074_849655_-|cytochrome-P450	gnl|CDD|225035	COG2124, CypX, Cytochrome P450 [Secondary metabolites biosynthesis, transport, and catabolism].	1.11541e-41
NZ_CP010833.1|WP_075263299.1|842922_843357_-|hypothetical-protein	gnl|CDD|225557	COG3012, COG3012, Uncharacterized protein conserved in bacteria [Function unknown].	1.97787e-41
NZ_CP010833.1|WP_075263297.1|840156_842247_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.29683e-74
NZ_CP010833.1|WP_075263300.1|843456_844266_-|SAM-dependent-methyltransferase	gnl|CDD|252734	pfam04672, Methyltransf_19, S-adenosyl methyltransferase. This family contains a SAM (S-adenosyl methyltransferase) domain, with a central beta sheet with 3 alpha-helices on both sides. Crystal packing analysis of the structure Structure 3giw suggests that a monomer is the solution state oligomeric form. An unidentified ligand (UNL, cyan) was found at the putative active site surrounded by the residues His57, His170, Phe171, Tyr216 and Met22. The UNL is likely to be a phenylalanine or phenylalanine-like molecule. (details derived from TOPSAN).	1.39695e-130
NZ_CP010833.1|WP_075263298.1|842272_842860_-|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	2.68855e-21
NZ_CP010833.1|WP_075263292.1|834250_835465_+|helix-turn-helix-domain-containing-protein	gnl|CDD|379258	pfam13556, HTH_30, PucR C-terminal helix-turn-helix domain. This helix-turn-helix domain is often found at the C-terminus of PucR-like transcriptional regulators such as Bacillus subtilis pucR and is likely to be DNA-binding.	2.27278e-11

Protein sequences

>NZ_CP010833.1|WP_075263296.1|839007_839868_+|hypothetical-protein
MSPVLLTGGEDHRPSLLLVTDLGYEARGRRYCDEDIFLASRLREAFDVALCHPRDAAVLLDRFDLALVRNSGPVLHYREAYDAFRARALELRVPVYNPLDGRGDMAGKEYLVEMSAAGLPVIPTVDRAAELPGLPDVARYVVKPKLGADSVGLRFVTAAEARAELEAAAEGSLLVQPRIDFRHEVSFYFVDHDFQYALYAPDPERRWVLEPYAASTEDLEFARRFIAWNTLDHGIQRVDACRTADGALLLVELEDLNPYLSLERVGEDVREAFVARLKTSIASLPR
>NZ_CP010833.1|WP_159024699.1|838701_838878_+|hypothetical-protein
MTSTSTQPTPARPMVELNAEIRALVADGGVVSPEGRREYERLLVEWVAAVRGSSAEAV
>NZ_CP010833.1|WP_093812656.1|837816_838353_+|excalibur-calcium-binding-domain-containing-protein
MDWNSSQHPSRQPGWGQGGNFTPQPPSTGGPRWARKRVVLPAAGVLFLLGVGIGATGEQPQEVRTVAAKAKPGPTVTVTETATVTVTATPEPAPTVTKVKKVRVTVTAAPPEPEPKPAKKPVARDDSTGGSGGSGSGGSSAYYKNCDAVRAAGAAPIRSGQPGYGRHLDRDGDGVGCE
>NZ_CP010833.1|WP_075263294.1|836480_837695_+|acyl-CoA-dehydrogenase
MSFFSLALTEEQRDLRDWVHGFAAQVVRPAAAEWDAREETPWPVIQEAARIGLYGFESLADLYGDPTGLSLQIANEELFWGDAGIGMALFGTSLAVAGIFASGTPDQLAEWVPQCYGDEEDPKVAAFCVSEPGAGSDVSAMTTRARYDEAADAWVISGQKAWITNGGIAEVHVVVASVDPSLGSRGQAAFIVPPGTKGLTAGRTVKKLGLRASHTADLFLDDVRVPGHCLLGGKEKLDARLARAREGSTAKGQAAMATFEVSRPTVAAQALGIARAAYEYALEYAGEREAFGRPIIENQSIAFALADIRTEIEAVRLLIWQAAWMARNDRTFDAGQGSMSKLRAGELAVAATEKAVQILGGAGYSREHPVERMYRDAKIYTIFEGTSEIQRLVIARAISGRQIR
>NZ_CP010833.1|WP_075263293.1|836002_836476_+|SCP2-sterol-binding-domain-containing-protein
MDGTSSGNLTDDLSALDFAAVAPEEFARIVKGLSAKQLAEVMRGDLRTRILGEVFGRMRQQFRSEAAGGLTALIRWKITGESDAVYETAIADGACRVTAGRSDAEPRTTLVMADAEFLKLVSGNGNPVTMFMTRRLKVAGDVGLASGLTRYFDIPKA
>NZ_CP010833.1|WP_010058123.1|835666_835930_+|hypothetical-protein
MTASHLLVPVPIPDRVAALIGSCIPPHILQAEFDADCAAREVRRFRGPRLGVEDQADREQALSELARANKVLAAHHPHLAVLPGSPF
>NZ_CP010833.1|WP_075263292.1|834250_835465_+|helix-turn-helix-domain-containing-protein
MPHLIQPLDTEDPLGPLPQEFAAIMRPELPSLIKEIGVEVTRAYPEYARLLDGPNGQAIRVGVEQSLASFVDLVAEPSSPTTLRDDMCRRFGRFEAYEGRSMDTLQGAYRLGARVALRRAKKVGQSYHLSPTLMLSFADALFAYVDELESLSREGFLEAQSQSGEHSEALRRRLLHLILAGRPAPGSAIADLCEQTRWTLPEEVTLIAVRAPAELDRLSADRDLLVDLSAPQPHLLVPGALDDARRSMLTQALPAGRMAIGLTVPTALACESLRWARRVLELVDSGVIEDAPLIRCEDHLLTLWLLSDPALLDQLAQRELAAVAGISATRRERLVETLRIWLDTRGTAAQMGALLDVHPQTVRYRMRSLETIFGDQLVDPESRFATEAVLRALRLRSRATGTSP
>NZ_CP010833.1|WP_075263291.1|832506_833442_-|hypothetical-protein
MRSVSNRTRVGLLAAFTAFSALLSTGSATAATQLNGDWAPFDRCPVDAPAMLAADGVNTIAACIASSSATGSITLGKSVVSTGHTDLQLGVVQRADGTASLVAPPEGALTADPAEIPGGLLGLMCPSGIPLVSGICRQLTDNNLNRVTATIEPAGAPRDFNMSAAFSTGEPILTIPVRIHLKNPFLGDKCYIGTTANPVLLKPQNVTAPTLSLQRFGADGTPNDDEGEMGRYTFDGADQGDATFAVPGASGCGAGLLDWAVNLKTGLPSAAGKNSVTLDATTTYFGSPYDPAGLAPNEGRKLSEFWHSAKR
>NZ_CP010833.1|WP_075263290.1|831624_832281_-|hypothetical-protein
MFKRTGFLTAIGAAAASVVLAAPSAVAAPTSWTITPTGNFNGSAGVTVLTDNNGNKIQCATSAASGNAPTSPVAGSPAKLASITAISFNSPCTGPFSSTWTVTTTPPWEIWGLDYTAGAGTNSTGQVTGEIRAIKAKVSGSSILGPCTFDVTGKVAAKYNNPTAGGSNGTLNTAGGGLTLSIANKVGGGCGIVGTTASFQGLYTLVSATTGKSPVISG
>NZ_CP010833.1|WP_075263289.1|829760_831272_-|hypothetical-protein
MTVDARAAARRPIHWAVGGALVVATALVPSAESTAAEQKSEVSLRYTCPFPSGPEEVDVVVSAVLPTSARTGEEIRPAEAAVEVTLPPTALARFADLDAATLSAVARLTVRNTVGDKSADASWQDLTAPPADLPAPGEGDGQDPGALTLTATGDVPTVAFGSPGRATLAPDALALALTSLTEAGEPTTPPGLDVACTPAPGQEPELAAIAIRGDQDPTAPAPRPGESDPVPDPTPTRPAEGLPPTAREKIDALTGKRREALEDDPGSCPIEIPPEWVMTTAETYAAGYANAAKLDGAAALGPAFMKVVLNKRYINDSCASTVDVSSEVNFDYQGKRQLPPTKATFLSYGFMPTTATMTLEQVGPPAAIHTHTVTNTPTYPEETTVTARLVMRLSDVEVNGVPLDVGPDCRTERPFEQVLKGYGQSYPPAGYLVAYGGTLTGYAHIPPFEGCGATEDLDPIFTSAISSPGKKADNYTKMTQAPLCVATNPEGPDCPPRAPDPER
>NZ_CP010833.1|WP_075263297.1|840156_842247_+|MFS-transporter
MTTASEQAPAAQSAAPPPVLDRRRRNIVFTTIVLGMLLAALDQTIVGTALPTIVSDLGGASHMSWVVTAYLLAETVATVLVGKFGDLFGRKLVFQVSAIIFITGSFLCGLASDMLLLIIWRGMQGIGAGGLMVTSMALIADVIPLRERGKYQGAIGAVFGISTVIGPLLGGLFTDHLTWRWAFYVNVPIAIVVVIAAARNIPSVKAAGRPSIDYTGIALVSVGASALILATSWGGNEYAWGSAVIIGLFVGGLIALALFCVVETRAKEPMLPMRLFRNPVFTVCSILSFIVGFAMLGSMIFLPTYLQYVDGDSATLSGVRTLPLVAGLLAASIFSGNVVSKTGRYRVFPIVGTLVMAAGLFLLSRMGPGTGVWLESLYMVVLGLGIGLAMQVLTIAVQNTVDYEDLGTATSGVTFFRTLGSAFGTAVFGTIYANALKPNLTDGVAQAVAAGGDPAVLARASESPQALHALPAAQSEPLAQAYADTLHTVFLWTVPVALIGFVIALFLKEVKLRDSARLGSTDMGEGFAQPGSGDSAKVLEYSVATILHNAGPETARRITAECDTRLDMAGAWAVMQVDLFTRMVGHAGLGLIAARHRIPPEVLVPVFDRMIEEGYLTGDGRIFSHTAAGRREAAVISDAWGRWLNDRLAEDGARPDDRQLRATVDVIAKRLLAEDLAQELSPAAGPGGSSRVGAPV
>NZ_CP010833.1|WP_075263298.1|842272_842860_-|GNAT-family-N-acetyltransferase
MDEDEAATPYAARERFWRGRDVAFTPLEPDDAELIHSWRAEPVAAHEMGVWPGSLHEFRERVEAHVENRDRDDFLVLLPDGTPVGHIALIEEDLVDGTAEACLLLAAAHRRRGLGADALAALTDLAFGELGLHRVEAVTHTDNTAALATLRGAGFVHEGVRRSSCLHRGRRYDNAILGLLRAEWETLERPRSWEH
>NZ_CP010833.1|WP_075263299.1|842922_843357_-|hypothetical-protein
MSRRTPRPRGTAAPRITPASPCPCGLPAAYGECCGRYHSGSAAAPTCEALMRSRYAAFVVQDAAYLLRTWHPETRPPGVDFDPSMRWLGLDILDTTEGSAFHSTGTVTFRAHYTDDGRPDSLHEKSRFVRHEGAWVYATAVFVD
>NZ_CP010833.1|WP_075263300.1|843456_844266_-|SAM-dependent-methyltransferase
MTGQEPPSTEIDTSRPHPARMYDWFLGGKDNYPVDEQMARQLLTLDARGRDMARVNRAFMHRATRWLAERGVRQFLDIGTGIPTEPNLHQIAQQAAPEARVVYCDNDPIVLAHAAALLRSTPEGATEYIQADARRPETILAEAGKVLDFEQPIALSLLALLHFIDDEDGAAALVGKLVDQLPSGSYLVLSHTTGDFDPEGAAQARAMYKARGMTLRPRSRAELTAFFDGLELVEPGVSLSADWHPELGEVIDVPGDEPIPGYAGVARKP
>NZ_CP010833.1|WP_010058136.1|844313_844550_-|DUF397-domain-containing-protein
MNHIYNGMPAGDLGSEGWYKPWSGGNGGNCIEAMKLADGRVAVRQSADPDGPALIYSNGEIAAFIQGAKAGQADFLLT
>NZ_CP010833.1|WP_075263301.1|844549_845410_-|helix-turn-helix-domain-containing-protein
MSEPRSAPTVGQVVLGKRLQDLRERAGLTRDQAAKVLRVAPATIRRMETAEVGLKIPYVQLLLKAYGVADQEAEAFVDLAEEANRPGWWQRFHDVLPDWFSMYVSLEGAASLLRMYEPHFVPGLLQTEDYARSVMRTGAVGQTRPEDIERHVALRMERQSLLAKEDAPRLWVIMDETVLRRPVESAQVMRGQIDKLLEATELPHVTLQIAEFASGHHPGTYGPFVLFRFAVPELPDMVYSEYLTGAVYFDARPEVASYLEVMDRMAAQAATAQRTKEILRDFRKEL
>NZ_CP010833.1|WP_075263302.1|845617_846094_+|ATP-binding-protein
MAPGSALIPRLTDLSPGTEALRYCFALPAHPESVAGARELTRARLDAWKLGRDACDATVLIVSELVTNAVVHTASTRVVCELSRFGRRLRIAVQDQGHQPCGPRLRPSSDDEHGRGLLLVDAMSSAWGSHDAGDSSGRIVWAELPHGAEQLSGAERAC
>NZ_CP010833.1|WP_075263303.1|846087_846525_+|hypothetical-protein
MLRNALARLRAAHRGRTPEQVGGGRVRLALPASMSATLGCDAVGVPARHGFRLMSHLPRTGCVFADADRWWWIVPAGSDLDLDWPEQVTYARDAAVPGSRPRLIHSPDALTPYTPPIPLFLMVCQVTGVTPSWAAPGRRSVVASG
>NZ_CP010833.1|WP_075263304.1|846604_847951_-|6-phospho-beta-glucosidase
MKLTILGGGGFRVPLVYGALLGDHAEGRVSRVTLYDTDADRLTAVARVLAEQGRDIADAPAVVATTELDEALRGADFVFSAIRVGGLAGRAADERVALDEGVLGQETVGAGGIAYGLRTVPVALDLARRIARLAPRAWVINFTNPAGLVTEAMSRHLGDRVIGICDSPVGLGRRIARVLGADPDRAWIDYAGLNHLGWVRGLYVDGRDELPRLLADPKLLESFEEGRLFGAELLRSLGAIPNEYLHYYYVNREAVRAYQEAEQTRGAFLRDQQEGFYARMREPGTPAWATWDRTRAEREATYMAENREVAGAGEREESDLESGGYEQVALALMRAVARNERTSLILNVRNRTTLSVLDADAVVEVPCLVDANGAHPVTVSPLPYHAVGLVTAVKAVERAVLEAAGSGSRAAAVQAFALHPLVDSVTVARRLLDRYTEVHPGLAYLGRA
>NZ_CP010833.1|WP_075263305.1|848074_849655_-|cytochrome-P450
MTTPFHHEPGTVPPPQCPAHNLDIGPGGLRRLHGPEAENNPAGLYDKLRAEHGTVAPVLLHGDVPAWLVLGHSENLHLTRTPSQFSRDSRRWRALQDGSVAPDHPLAPIFTWQPVCVFADGAKHERQRGAVTDSMERIDTRGVRRHINRFSNRLVNDFCEKGTADLVSQFAEHLPMMVMCAIFGMPEEYDERLVQAARDMTRGTETAVASNAHIVAVLTRLVERRRAEPAHDFASWLVEHPATMTDIEVVEHLRLILIAAYESTANLIANVLRMVLTDPRFRARLSGGHMTVPEAVEQTLWDEPPFTAVFGRWAVGDTELGGQQIKAGDALLVGIAPANTDPTVRPDLNADMGGNRAHLAFSGGPHECPGQDIGRAIADVGVDALLMRLPDLELGVGESELRWVGNIMSRHLVELPVTFAPSPQQKLDADPLSVMARTPRPADAWEISSPARTVPEPRHEAAAGAQSADAPGTTPRPTPAAAPPAAQPAPAAPAPEAAPVATIPRQRRPAAPARLWQAVTRWWNGY

Crispr_ID: NZ_CP010833_5

• CRISPR_ID: NZ_CP010833_5
• CRISPR_location: 962292-962419
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_5

Consensus_repeat	Method
CGGCCCGCTCCCGTTCGGGGGCACGCTCCCGCCCA	CRISPRCasFinder

spacers of NZ_CP010833_5

>5.1|962327|58|NZ_CP010833|CRISPRCasFinder
CCCGCCGGGCCCTGTGCGCCGGCCCGGCCCCAACCGTGCGCCCCGCCTTCCGACTCAC

CRISPR arrays and Neighbor proteins around NZ_CP010833_5

CRISPR arrays

The CRISPR arrays of NZ_CP010833_5

>merge|NZ_CP010833|5|962292-962419|CRISPRCasFinder
CGGCCCGCTCCCGTTCGGGGGCACGCTCCCGCCCACCCGCCGGGCCCTGTGCGCCGGCCCGGCCCCAACCGTGCGCCCCGCCTTCCGACTCACCGGCCCGCTCCCGTTCGGAGGCACGCTCCCGCCCA

>NZ_CP010833|5|5|962292-962419|CRISPRCasFinder
CGGCCCGCTCCCGTTCGGGGGCACGCTCCCGCCCA	CCCGCCGGGCCCTGTGCGCCGGCCCGGCCCCAACCGTGCGCCCCGCCTTCCGACTCAC
CGGCCCGCTCCCGTTCGGAGGCACGCTCCCGCCCA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075263385.1|968811_969051_-|LapA-family-protein	unknown	unknown	gnl|CDD|377648
NZ_CP010833.1|WP_075263375.1|952021_954154_-|NAD-dependent-DNA-ligase-LigA	unknown	unknown	gnl|CDD|236137
NZ_CP010833.1|WP_075263379.1|957129_959298_-|hypothetical-protein	unknown	unknown	gnl|CDD|377198
NZ_CP010833.1|WP_003965046.1|965314_965668_+|glyoxalase/bleomycin-resistance/dioxygenase-family-protein	unknown	unknown	gnl|CDD|319911
NZ_CP010833.1|WP_075263376.1|954370_955309_+|DUF1996-domain-containing-protein	unknown	unknown	gnl|CDD|370451
NZ_CP010833.1|WP_075268230.1|961005_962157_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl|CDD|99734
NZ_CP010833.1|WP_075263381.1|962792_964307_+|bifunctional-phosphatase-PAP2/diacylglycerol-kinase-family-protein	unknown	unknown	gnl|CDD|224513
NZ_CP010833.1|WP_075263380.1|960330_960969_+|hypothetical-protein	unknown	unknown	gnl|CDD|223659
NZ_CP010833.1|WP_075263383.1|965707_967693_-|DUF5107-domain-containing-protein	unknown	unknown	gnl|CDD|375006
NZ_CP010833.1|WP_075263384.1|967826_968723_-|arginase-family-protein	unknown	unknown	gnl|CDD|212523
NZ_CP010833.1|WP_075263382.1|964435_965245_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|181382
NZ_CP010833.1|WP_075263374.1|950743_951460_-|rod-shape-determining-protein-MreC	unknown	unknown	gnl|CDD|212668
NZ_CP010833.1|WP_075263386.1|969192_970950_-|CocE/NonD-family-hydrolase	unknown	unknown	gnl|CDD|334820
NZ_CP010833.1|WP_075263388.1|974219_975563_-|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|181163
NZ_CP010833.1|WP_075263373.1|950075_950747_-|hypothetical-protein	unknown	unknown	gnl|CDD|237057
NZ_CP010833.1|WP_075263378.1|956089_957142_+|LacI-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224525
NZ_CP010833.1|WP_075268229.1|959557_960334_+|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|225130
NZ_CP010833.1|WP_075263377.1|955428_956055_+|DUF305-domain-containing-protein	unknown	unknown	gnl|CDD|367619
NZ_CP010833.1|WP_075263387.1|971170_972133_-|LD-carboxypeptidase	unknown	unknown	gnl|CDD|132882
NZ_CP010833.1|WP_075268231.1|972129_974148_-|prolyl-oligopeptidase-family-serine-peptidase	unknown	unknown	gnl|CDD|224423

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075263385.1|968811_969051_-|LapA-family-protein	gnl|CDD|377648	pfam06305, LapA_dom, Lipopolysaccharide assembly protein A domain. This family includes a domain found in lipopolysaccharide assembly protein A (LapA). LapA functions along with LapB in the assembly of lipopolysaccharide (LPS). Domains in this family are also found in some uncharacterized bacterial proteins.	0.00456315
NZ_CP010833.1|WP_075263375.1|952021_954154_-|NAD-dependent-DNA-ligase-LigA	gnl|CDD|236137	PRK07956, ligA, NAD-dependent DNA ligase LigA; Validated.	0
NZ_CP010833.1|WP_075263379.1|957129_959298_-|hypothetical-protein	gnl|CDD|377198	pfam04020, Phage_holin_4_2, Mycobacterial 4 TMS phage holin, superfamily IV. These proteins are predicted transmembrane proteins with probably four transmembrane spans. The 1.E.40 is represented by the mycobacterial 4 phage holin, but it also contains many cyanobacterial. proteobacterial and firmicute proteins. Holins are encoded within the genomes of Gram-positive and Gram-negative bacteria as well as in those of the bacteriophage of these organisms. The primary function of holins appears to be transport of murein hydrolases across the cytoplasmic membrane to the cell wall where these enzymes hydrolyze the cell wall polymer as a prelude to cell lysis. When chromosomally encoded the enzymes are therefore autolysins. Holins may also facilitate leakage of electrolytes and nutrients from the cell cytoplasm, thereby promoting cell death. Some may catalyze export of nucleases.	1.53667e-10
NZ_CP010833.1|WP_003965046.1|965314_965668_+|glyoxalase/bleomycin-resistance/dioxygenase-family-protein	gnl|CDD|319911	cd07247, SgaA_N_like, N-terminal domain of Streptomyces griseus SgaA and similar domains. SgaA suppresses the growth disturbances caused by high osmolarity and a high concentration of A-factor, a microbial hormone, during the early growth phase in Streptomyces griseus. A-factor (2-isocapryloyl-3R-hydroxymethyl-gamma-butyrolactone) controls morphological differentiation and secondary metabolism in Streptomyces griseus. It is a chemical signaling molecule that at a very low concentration acts as a switch for yellow pigment production, aerial mycelium formation, streptomycin production, and streptomycin resistance. The structure and amino acid sequence of SgaA are closely related to a group of antibiotics resistance proteins, including bleomycin resistance protein, mitomycin resistance protein, and fosfomycin resistance proteins. SgaA might also function as a streptomycin resistance protein.	2.53569e-08
NZ_CP010833.1|WP_075263376.1|954370_955309_+|DUF1996-domain-containing-protein	gnl|CDD|370451	pfam09362, DUF1996, Domain of unknown function (DUF1996). This family of proteins are functionally uncharacterized.	3.93734e-63
NZ_CP010833.1|WP_075268230.1|961005_962157_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl|CDD|99734	cd00609, AAT_like, Aspartate aminotransferase family. This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). Pyridoxal phosphate combines with an alpha-amino acid to form a compound called a Schiff base or aldimine intermediate, which depending on the reaction, is the substrate in four kinds of reactions (1) transamination (movement of amino groups), (2) racemization (redistribution of enantiomers), (3) decarboxylation (removing COOH groups), and (4) various side-chain reactions depending on the enzyme involved. Pyridoxal phosphate (PLP) dependent enzymes were previously classified into alpha, beta and gamma classes, based on the chemical characteristics (carbon atom involved) of the reaction they catalyzed. The availability of several structures allowed a comprehensive analysis of the evolutionary classification of PLP dependent enzymes, and it was found that the functional classification did not always agree with the evolutionary history of these enzymes. The major groups in this CD corresponds to Aspartate aminotransferase a, b and c, Tyrosine, Alanine, Aromatic-amino-acid, Glutamine phenylpyruvate, 1-Aminocyclopropane-1-carboxylate synthase, Histidinol-phosphate, gene products of malY and cobC, Valine-pyruvate aminotransferase and Rhizopine catabolism regulatory protein.	1.76635e-20
NZ_CP010833.1|WP_075263381.1|962792_964307_+|bifunctional-phosphatase-PAP2/diacylglycerol-kinase-family-protein	gnl|CDD|224513	COG1597, LCB5, Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase [Lipid metabolism / General function prediction only].	3.62591e-21
NZ_CP010833.1|WP_075263380.1|960330_960969_+|hypothetical-protein	gnl|CDD|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	5.01357e-17
NZ_CP010833.1|WP_075263383.1|965707_967693_-|DUF5107-domain-containing-protein	gnl|CDD|375006	pfam17128, DUF5107, Domain of unknown function (DUF5107). This family is found in range of different bacterial species. In many proteins it lies N-terminal to a TPR-repeat region at the C-terminus.	6.25477e-34
NZ_CP010833.1|WP_075263384.1|967826_968723_-|arginase-family-protein	gnl|CDD|212523	cd09999, Arginase-like_1, Arginase-like amidino hydrolase family. This family includes arginase, also known as arginase-like amidino hydrolase family, as well as arginase-like proteins and are found in bacteria, archaea and eykaryotes, but does not include metazoan arginases. Arginase is a binuclear Mn-dependent metalloenzyme and catalyzes hydrolysis of L-arginine to L-ornithine and urea (Arg, EC 3.5.3.1), the reaction being the fifth and final step in the urea cycle, providing the path for the disposal of nitrogenous compounds. Arginase controls cellular levels of arginine and ornithine which are involved in protein biosynthesis, and in production of creatine, polyamines, proline and nitric acid.	1.65506e-76
NZ_CP010833.1|WP_075263382.1|964435_965245_+|methyltransferase-domain-containing-protein	gnl|CDD|181382	PRK08317, PRK08317, hypothetical protein; Provisional.	3.79971e-33
NZ_CP010833.1|WP_075263374.1|950743_951460_-|rod-shape-determining-protein-MreC	gnl|CDD|212668	cd10225, MreB_like, MreB and similar proteins. MreB is a bacterial protein which assembles into filaments resembling those of eukaryotic F-actin. It is involved in determining the shape of rod-like bacterial cells, by assembling into large fibrous spirals beneath the cell membrane. MreB has also been implicated in chromosome segregation; specifically MreB is thought to bind to and segregate the replication origin of bacterial chromosomes.	6.12329e-08
NZ_CP010833.1|WP_075263386.1|969192_970950_-|CocE/NonD-family-hydrolase	gnl|CDD|334820	pfam02129, Peptidase_S15, X-Pro dipeptidyl-peptidase (S15 family).	3.43886e-22
NZ_CP010833.1|WP_075263388.1|974219_975563_-|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|181163	PRK07906, PRK07906, hypothetical protein; Provisional.	0
NZ_CP010833.1|WP_075263373.1|950075_950747_-|hypothetical-protein	gnl|CDD|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	0.000169505
NZ_CP010833.1|WP_075263378.1|956089_957142_+|LacI-family-transcriptional-regulator	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	3.30743e-102
NZ_CP010833.1|WP_075268229.1|959557_960334_+|MBL-fold-metallo-hydrolase	gnl|CDD|225130	COG2220, COG2220, Predicted Zn-dependent hydrolases of the beta-lactamase fold [General function prediction only].	2.10163e-30
NZ_CP010833.1|WP_075263377.1|955428_956055_+|DUF305-domain-containing-protein	gnl|CDD|367619	pfam03713, DUF305, Domain of unknown function (DUF305). Domain found in small family of bacterial secreted proteins with no known function. Also found in Paramecium bursaria chlorella virus 1. This domain is short and found in one or two copies. The domain has a conserved HH motif that may be functionally important. This domain belongs to the ferritin superfamily. It contains two sequence similar repeats each of which is composed of two alpha helices.	1.10739e-20
NZ_CP010833.1|WP_075263387.1|971170_972133_-|LD-carboxypeptidase	gnl|CDD|132882	cd07025, Peptidase_S66, LD-Carboxypeptidase, a serine protease, includes microcin C7 self immunity protein. LD-carboxypeptidase (Muramoyltetrapeptide carboxypeptidase; EC 3.4.17.13; Merops family S66; initially described as Carboxypeptidase II) family also includes the microcin c7 self-immunity protein (MccF) as well as uncharacterized proteins including hypothetical proteins. LD-carboxypeptidase hydrolyzes the amide bond that links the dibasic amino acids to C-terminal D-amino acids. The physiological substrates of LD-carboxypeptidase are tetrapeptide fragments (such as UDP-MurNAc-tetrapeptides) that are produced when bacterial cell walls are degraded; they contain an L-configured residue (L-lysine or meso-diaminopimelic acid residue) as the penultimate residue and D-alanine as the ultimate residue. A possible role of LD-carboxypeptidase is in peptidoglycan recycling whereby the resulting tripeptide (precursor for murein synthesis) can be reconverted into peptidoglycan by attachment of preformed D-Ala-D-Ala dipeptides. Some enzymes possessing LD-carboxypeptidase activity also act as LD-transpeptidase by replacing the terminal D-Ala with another D-amino acid. MccF contributes to self-immunity towards microcin C7 (MccC7), a ribosomally encoded peptide antibiotic that contains a phosphoramidate linkage to adenosine monophosphate at its C-terminus. Its possible biological role is to defend producer cells against exogenous microcin from re-entering after having been exported. It is suggested that MccF is involved in microcin degradation or sequestration in the periplasm.	4.3196e-94
NZ_CP010833.1|WP_075268231.1|972129_974148_-|prolyl-oligopeptidase-family-serine-peptidase	gnl|CDD|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	8.51297e-56

Protein sequences

>NZ_CP010833.1|WP_075268230.1|961005_962157_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MPVLPELAAVLAAASARTRPEPPGGGPVLREAARGYWERRGLHGTAGGIAAAPGAQPLLLALIGAHGGDVLMPRPCPATWMPQARLLGRPAYHVPTPAECGGIPDPYALLETVRRVRAEGGRPKLLLLSVVDDPTATVAPPELVREACEAAVGEGLHIISDETWRDTVHRPRDTVLLSPAEMCPDDVTVLADLSGALAPAAWPVAVARFPDNPRAAVRHARTLDILTALGALVAGPVAHAAAHALGEPDSVRDRIRRAAALQTEVAAAAHRAVLGSGALARPPQAGRHLYTDLGPLRSRLADLGVTDSMELEEYLTDRLGAPAPGGHRFGDELGALRVRLGTGPLLGATPQQQTESLAAAKPLELPHVAQALDGLAAVFAELR
>NZ_CP010833.1|WP_075263380.1|960330_960969_+|hypothetical-protein
MIQEIQQVVRELPTESTQQAVGYPTLFALVSLGSLVPVVPTGALVSSAAVVAFHQTSPLALLFVFLVASAAAFLGDVCLYWLGQRGVRSNHGSKWLAAITRRAAPERLAQAQEKLAEHGGTVLVLSRLVPAGRIPVMLACLLGRMPLRQFARGDVPACLAWAATYQLIGILGGSLFPEPWQGVVAAVALTLLISGAPAVWRRLRERFGPASS
>NZ_CP010833.1|WP_075268229.1|959557_960334_+|MBL-fold-metallo-hydrolase
MEVTWWGHATCTIEDSGVRVLTDPLFVRRFAHLRRRRGEVPPPEAAVAEVVLVSHLHSDHLHLPSLARLAPGSRLIVPSGAVAAVPGLRMLRRVRQLHITEVRPGDTVRIGEVRVRAVPALHDGRRLPVGPHRSPALGYVVEGEARTYFAGDTGLFDAMADAVGPVDMALLPVGGWGPYLGHSHLDPARAAEALTRLAPRSAVPVHYGTYWPIGMDAVRPHEFHAPGDEFVRHAAKRAPEVAVHLLGHGERVRPEAGR
>NZ_CP010833.1|WP_075263379.1|957129_959298_-|hypothetical-protein
MGDGKWRTAGRALLRVTAVWAVSTLTMLVLAGALPDFQLQSDDGDTITKTAFTAAWGAGAFGLLSALVWPVLVRALLIVPALVLGALVFFLNGSLLLIALRLIPDGRGDAAPETAVVVAAVMSAVASATSTALAVRDDEAYRRRLSRLADRRRRRGRSPDPAEPGREGPPGTVFLQLDGVGHDVLVKAAAAGLMPTVAGWLADSSGHRLTPWRTDWSSQTGASQLAILHGSNHDVPAFRWYEKETRTVMVSSRPASALEMQRRAIRRTHDGGLLTVDGASRGNLFSGGAGQLALVLSMAARRGKGRRSRAGYFAYFSDPANATRTALSFVAEVFREIGQSTRARARKVTPRIKRGGLYPFIRAFATVVERDVVVAAVLGDMFAGRTAVYADLVAYDEVAHHSGPHSRDAEKVLVRLDRSLALIAKIADHTPRAYRIVLLSDHGQSPGETFAGKYGLMLKDLVRAGCGLPVPRRAQRTRSASEARDAVRIALHRPVEGQQDEHPAKPSDPIVLASGNLGLISFPDIEGRATREQIERRHPALLSTLANHPGIGFLLVGGEDGSVVLGRGGAEVPVAELTDGEGPLAGFDTGAADAVRRTDTFPHVADVMVNSMYDPGTGTVHAFEEQIGSHGGLGGEQSRPFLLWPRGLTDPLDIVAAETAEGAPPPPGGGLVGAEAVHRVLTRWLHESSGPQVPVRAEGFAGAGPADVPFPTGAPVPDAQAD
>NZ_CP010833.1|WP_075263378.1|956089_957142_+|LacI-family-transcriptional-regulator
MTAEVPQPVRPTTLEDVAAVAGVSRATVSRVINGATTVDPALRTVVEQAVATTGYVPNRAARSLVTRRTDSVALVVSERERRPMSEPFVGRMFSDPYFGRVVSGLLEVLRPAGIQMVVMLADDEASRTQLLSYLRHGHVDGVVLITTHADDPLPGLLQETRMPAVLAGRPHRPSPLAYVEVDQHAGARLAADHLAAQGRWRIGTITGPQDMPAGQVRLTGFLEACAAHGIEDVACAEGDFTHLGGAAAMRRLLADRPDLDGVFIASDLMALGALPVLLRAGRDVPSDVAVVGFDDSSAAAACDPPLTTVRQPVEEMAAEMARLLLKQIGEPGGPSPSVLFPPALVRRQSA
>NZ_CP010833.1|WP_075263377.1|955428_956055_+|DUF305-domain-containing-protein
MNPVSLPLPPLRRAAVLVLLCAPALGGAAGCSPPPGTPPPTPTATSTPTATATATATATDVGWVQLMTPMNQQAVKLLTLAATRAAEPRVRGFAGRLRTEQEAELDRLRSLLTRMGLPGTDVHAGHDMPGMVTVRDLEAARAAEGPAFDRLVLVQIRDHLRQSAQVSRSEITSGGRADARELAAALVTAREASLAELERLPGAGRALG
>NZ_CP010833.1|WP_075263376.1|954370_955309_+|DUF1996-domain-containing-protein
MLFRHRRNPDHRRPRSLPSWRYRIAGLAAAALALSFLQANVGNAAAERAAADATPKAAADVVRVAEFLAECPYTHRLPDDPIVFPGLPGASHMHSFFGNDTTHAGSDLASLEKGRTSCAPDTDLSSYWVPTLYDGDKEVEPTGTTFYYLGEGVSDDVIRQIKPFPRGLRIVAGNAKATGPQDNTIARWSCLHAGEVNPSQNFVNCPPGTMMESYLDFPQCWNGTDLDSPDHKSHMAYPVNGGCPSTHPVPVPKLRQVLRYPVNGDPARFRLASGPGYTMHGDFFNVWPEEEMAQRVRDCINAIVKCGFDGKP
>NZ_CP010833.1|WP_075263375.1|952021_954154_-|NAD-dependent-DNA-ligase-LigA
MVVMTNSAAVLADAAAYAAAVEEASVAAAAYYATGESGLDDDAYDRLARGIAAYEADHPEEVLAASPTGKVAGGAAVGDVPHTVPMLSLDNVFSAEQFAAWTASLERRIGRPVTAWSVEPKLDGLAVAARYRDGRFERLITRGDGTAGEDVSHAAGAVVGLPERLAEPVTIEVRGEILMTNDQFDQGNAIRTEHGGAPFANPRNGAAGTLRAKDRAYRVETTFFAYGALPLPDSGEFGETLAELPHSEVLSYVAGLGVHTAAGTDVAPVLAATAEEVQARVDAIGSLRAALPFGIDGIVIKADLAADQREAGSGTRAPRWAIAYKLPAVEKITRLVSVEWNVGRTGIIAPRAVLEPVEIDGSTVGYATLHNPADITRRDLRLGDQVMVYKAGDIIPRIEAPVVHLRTGDETPIDFPESCPQCGSAIDTSEQRWRCTRGRNCRLVASVSYAAGRDQLDIEGLGATRVVQLVDAGLVADFADLFTLEREQLLALDRMGETSTDNLLAAIETARTRPLSRVFCALGVRGTGRSMSRRIARYFATMDRIVAADVETLQRVDGIGTEKAAAVVAELVELAPLIAKLVAAGVNMTEPGATPPPEPGTEEVATAGADAEAGGDGGTGPMLPLAGMTVVVTGAMTGALEKLSRNQMNELIERAGGKSSSGVSKRTSLLVAGDKAGSKRTKAEDLGVRIAVPEEFAELVGAFLAAGEDG
>NZ_CP010833.1|WP_075263374.1|950743_951460_-|rod-shape-determining-protein-MreC
MPGRGLLLDPFPGSGLHGGAGRPVRRGRIVDPESCGLLLGRIADVALGPDRSDSVIVLSHPVLAGAEHRTAARALLAGLGTTRVVVLSSARAAAAYAGPRAAGPLLVVDMGAELTEVTLLVGGLVADARQAESGLDDLDGLDPATLPAVLVRTVLDMITSMWRHDRHGAIRGALRKGPVLAGGGALRSDVTDHLARCLGSRVRLADDPSTTVVRGAGQILSAVLRHRPTPPERSGRPR
>NZ_CP010833.1|WP_075263373.1|950075_950747_-|hypothetical-protein
MTPYPWPGRPRAYTPRVRCVLATLLLTVLTLVGGAATANGAAPAALASRSLAPAATAAAAPPPAAPRTHDSALASRHRPGHESALASRHRTGHDGAPDSRHHHAGPGPAHDVRHVVAQAEHEQPRAAADPAQAPRAGTGRAYLLLHAPPPPHDALTPAPAGPAAPRGGVHRVAAESFDAPGSRRGALPGVRGPPGRTTGPTTGHPPSCSDRSAPSADQASHPR
>NZ_CP010833.1|WP_075263381.1|962792_964307_+|bifunctional-phosphatase-PAP2/diacylglycerol-kinase-family-protein
MATPRTSPTASSAPAVARLRGWLQGRDLAVFRSVADRHWPGADPLLPRLSRSANHGLLWFGAAAGIAALGSSARSRRAALRGVASLAVASAAINTVGKGAVRRDRPILDAVPVMRQLKRQPVTTSFPSGHAASAAAFATGVALESKGWGAVVAPVAVAVAASRVYTGVHYPSDVLAGAALGVGAAFALRGVVPTRGQLPAPGRPPGEAPALPAGKDLVVVVNRESGTATATASLVREALPMATVMEVAPADLPTAFDEAAGQGRALGVCGGDGTVNLAASVAATHGLPLAVFPGGTLNHFAYDLGIETVHDTAVALTAGDAIRVDLGRFRPGPKGPDGADGYFLNAFSLGVYPELVNTREHWSSRIGGWPAGVLAAFHVLRGQRPLEAEFQGRRRPLWLVFVGNGLFRRVGPNPGRRHNLADGLLDVRVIHGGRGPALRLLAAAVAGPLTRSPVHAAVRRRRVRIGGLAPGTPYAYDGEVAHSGTELLIDKLPEALTVYCPMPV
>NZ_CP010833.1|WP_075263382.1|964435_965245_+|methyltransferase-domain-containing-protein
MSKDTAVYTHGHHESVLRSHRWRTAANSAAYLLDELRPGLAVLDVGCGPGTITADLAALVAPGRVTAVDAATDILGQAAAVADERGLENVEFAVADVHALEFPDDSFDVVHAHQVLQHVGDPVQALREMRRVCRPGGVVAARDSDYAAMTWYPETPGLDTWLDVYGRVARGNGGEPDAGRRLLSWARQAGFTDITPTAAAWCFATPESRAWWSGLWADRTTDSVYAELAVAGGHASAGQLTEIAGAWRSWGGEGDGWFMVPHGEVLCRV
>NZ_CP010833.1|WP_003965046.1|965314_965668_+|glyoxalase/bleomycin-resistance/dioxygenase-family-protein
MEILGTTLRICVDDLEAAVAFYEGLTGTSALRFERGGVSVAAIGCFLLMSGPESELEVLRKVGATIAVKDVDEANEALTRAGARVIAGPVPTPAGRNLIALHPDGSVFEYVDRNVTV
>NZ_CP010833.1|WP_075263383.1|965707_967693_-|DUF5107-domain-containing-protein
MATTVRRTVLNLPAAPLGPENPLPPLRPPAPPPVLDPRERAGLPRDMARQLGHRPLRTLLPTRLLDGYGRERTPTDLDAVVIENDRLRVTVLPGLGGRIHSLHHKPTGRELLHRNPVLQPAAFALNGAWFSGGIEWNIGATGHTTLTCAPLHAALVPAPDGGTMVRLWEWERLRDLPFQVDLWLPDDSDFLHVGVRIRNPHEQSAPVYWWSNIAVPETPDTRVLVPAGEAWHFGYDHTLTRVAVPESGGLDHTYPLRSEYPADHFYELPDGARRWIAALDADGHGLAQTSTDLLRGRKLFRWGHGKGGRRWQEWLNGPEGGGYAEIQAGLARTQLEHVPLEPSAAFSWLESYGPLSADPAAVHGGDWAAATGEAAARLEEALPRAAVEEAYAAWLPYADTEPGEVLATGSGWGALEVLRGGLRLPGTPFPTATLGEQQKPWRELLEHGILPKPDPEEPPCPTPVSRPWRDMLETADADPHTEYHLGIAQWHAGDRAQAVRSWERGLEKGPVPRWPLLRCLAVAAEESGRPDHAAELYAEAFADLGAPGTRDLAASEAGGALLVALARETVEAHLSAGRPGEARALLAGLPEAVRERGRFRLLLARALVAEGDTGAARAIFDAGFEVADLREGAGILGELWALVSDEPLPDAYDFRMSPPGA
>NZ_CP010833.1|WP_075263384.1|967826_968723_-|arginase-family-protein
MRTIVVLDAPSNLGLRPPAPGTVPGCYKLAGALREQRIVARLGALEGGVVVPPRYDLGDWQEGDGVFNAAAIARYTRTLADRIEGHVRAGEFALVLGGDCSIQLGAALALRRIGRYGLAAVDGSADFRHTGNSDRIGAAGGEELAIATGRGQADLSDIEGLGPYLKDEDVRLFGMRDEDEDQAELAALRIPNATVGQIRERGAADLARATVESLETPALDGYWVHLDADVLDPSVMPAVDSPDDGGLLPDELAPLLRTLVSSPRCVGLNVTIYDPDLDPDGTAGALLADLVVGALKEA
>NZ_CP010833.1|WP_075263385.1|968811_969051_-|LapA-family-protein
MSPKDVSSDSGRAQGWFTPGRIAVGVVVVLVIVFICVNTNDVTIRVLIPEVTMPLWSALAAMFLIGLGCGGYLFRRRGK
>NZ_CP010833.1|WP_075263386.1|969192_970950_-|CocE/NonD-family-hydrolase
MRGPLVAVAGAALVAPLVLAAPARADAAPYTVTPLTFTVDAGDRTCTVDADLYRPAGADADNPAPAVLATNGFGGSKSDGSTDTIGKAFAERGYVGLVYSGLGFGKSGCLITLDDPAVDGQAASELLDFLGGVRAADDGTRADFVTRDADGDPRVGMIGGSYGGAIQLATAAVDPRVDALVPLITWNDLAYALAPNNTGARTGVTSDTPGVFKWQWANGFYLIGEGQPLLNPSLDPSRINRLDCLHFATRACETIRLLNSGRYPADKTQEMLAYARSVSPVSYLDRVKAPTLIVQGQADSLFNLNEATATYRTLKAQGTDTKMIWQSWGHSGGQVPGELDLSQGNLETSHVGQRVLAWFDRYLHKNTGADTGPAFSYYRDWQSGYGTAADVPALSQSLYLSGDGKLVDNRSKVARGSRQYTNWLVPTSHSESSIAPLIGLPDPKPYDTKGTYLGWRSEPLTAPLDVVGAPKATLKVVSPKAERVQHSGDASDKLVLFAKVYDVAPDGSRKLVNRLVSPVRVPDVTRPFTVELPGIVHRYEKGHRLEFVIAASDTAYFGNRGIKPVTVLHAPEDTGVLELPVVPAG
>NZ_CP010833.1|WP_075263387.1|971170_972133_-|LD-carboxypeptidase
MTRQDDGPATPLARPARLRPGSRVAVVAPSGPVPADRLEEGLAVLRDWGLEPVVGPHASSTHPELDYLAGTDADRAADLQAAWCDPSVEAVFCARGGFGAHRMVDLVDWAAIRAAGPKAFVGYSDITVLHEAFALRAGFATLHGPMVATETFLKDAPTREHLRATLFEPETVRTLGLASAGTLVPGRAEGVLYGGCVSLLAADTGTPGGRSHARGNLLVIEDTGEEPYRLDGILTRLLRSGALTGVAGVACGSWQECGPYEKIRAVLADRLGPLGIPVVEELGFGHGTTALTIPLGLPAVLDAPSDGGRCTLTVKAPALL
>NZ_CP010833.1|WP_075268231.1|972129_974148_-|prolyl-oligopeptidase-family-serine-peptidase
MNTVPAAAPYGTWPSPIDAALAASRDGRPDHLGTVGDEIWWTEPRPAEGGRRALIRRRADGTTAPALPAPWDARSRVIEYGGQPWAGTVREDGGLLVVFVHFTDQRLYAYAPDGPDEPWPLTPVSEVGGGLRWVDPQVRPEQGAAGEVWCVLEEFTGPGPTDVRRVVAAVPLDGSAADDRTAVRELSDGRHRFVTGPKVSHDGRRAAWIAWDHPAMPWDGTVVMLADLTEAGEFTGVRPLVGDLDESVCQVEWDRDGSLLFVSDLSGWWELQRIRPDAVTGGAVPSSRLLPPRGEEFGGPLWKIGLRWFHPLDNGLIAVLHGKGDHRLGILDPETGELADAPGPWTVWSDTLAVHGSRVVGVAASPRSAPEVVELDTTTGRPRTIGAPHEDPVDPAYYPVPEHRTVTGPDGREIHAHIHPPHHPEHTGAQGEKPPYVVWAHGGPTGHTPLVLDLEIAYFTSRGIGVAEVNYGGSTGYGRAYRERLRGEWGLVDVADCAAVASALVEEGAADPDRLAIRGGSAGGWTAAASLTSTDLYACGTILYPILDLEGWATDETHDFESRYLESLVGPFAEVPERYRERSPMNRTDRLTTPFLLLQGLDDVICPPAQSERFLAAVSGRGIAHAYIAFAGESHGFRRVETLIRALEAELSLYAQTFCFDRSDVPPLELTT
>NZ_CP010833.1|WP_075263388.1|974219_975563_-|M20/M25/M40-family-metallo-hydrolase
MAEAPDLLGPVDQQALDEVVAFTSGLIRIDTTNRGGGDCRERPAAEYVAERLADAGIEPTLLERTPGRTNVVARIPGTDPSADALLVHGHLDVVPAEPADWTVHPFSGEVRDGVVWGRGAVDMKNMDAMVLSVVRGWAREGFRPPRDIVIAYTADEEDSAADGSGFLAEQHADLFEGCTEGISESGAFTFHAGDGLALYPIAAGERGTGWLKLTAEGRAGHGSKVNRENAVSALAAAVARIGEHEWPIRLTPTVRAAITEIAALHGITADLDDPGFDVAQLLGKLGPAASLVENTIRNSSNPTMLDAGYKVNVIPGHATAYVDGRMVPGGDEEFHTTLDRLTGPSVSWEFYHREQALTAPVDSPTYAKLRAAVERFDPGAHTVPYCMSGGTDAKQFSRLGITGYGFTPLKLPVGFDYQRLFHGVDERVPVDALHFGVRVLDHYLRTA

Crispr_ID: NZ_CP010833_6

• CRISPR_ID: NZ_CP010833_6
• CRISPR_location: 1086576-1086691
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_6

Consensus_repeat	Method
TGCGCGGCGACGCGGAACCGCCACACCG	CRISPRCasFinder

spacers of NZ_CP010833_6

>6.1|1086604|60|NZ_CP010833|CRISPRCasFinder
CTGAGCCCGCCTCCGGTGCGCGGCGACGCGGACCCGCCACGCCGGTGAGCCCGCCCTCGG

CRISPR arrays and Neighbor proteins around NZ_CP010833_6

CRISPR arrays

The CRISPR arrays of NZ_CP010833_6

>merge|NZ_CP010833|6|1086576-1086691|CRISPRCasFinder
TGCGCGGCGACGCGGAACCGCCACACCGCTGAGCCCGCCTCCGGTGCGCGGCGACGCGGACCCGCCACGCCGGTGAGCCCGCCCTCGGTGCGCGGCGACGCGGACCCGCCACACCG

>NZ_CP010833|6|6|1086576-1086691|CRISPRCasFinder
TGCGCGGCGACGCGGAACCGCCACACCG	CTGAGCCCGCCTCCGGTGCGCGGCGACGCGGACCCGCCACGCCGGTGAGCCCGCCCTCGG
TGCGCGGCGACGCGGACCCGCCACACCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075263450.1|1078586_1079234_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_075263451.1|1079701_1080571_-|precorrin-6A-synthase-(deacetylating)	unknown	unknown	gnl|CDD|236218
NZ_CP010833.1|WP_075263454.1|1083763_1084831_+|enoyl-CoA-hydratase/isomerase-family-protein	unknown	unknown	gnl|CDD|235533
NZ_CP010833.1|WP_075263456.1|1085753_1086563_+|enoyl-CoA-hydratase	unknown	unknown	gnl|CDD|180295
NZ_CP010833.1|WP_075263455.1|1084827_1085757_+|3-hydroxyisobutyrate-dehydrogenase	unknown	unknown	gnl|CDD|130753
NZ_CP010833.1|WP_075263459.1|1088888_1090538_+|pentachlorophenol-monooxygenase	unknown	unknown	gnl|CDD|235728
NZ_CP010833.1|WP_075263462.1|1094647_1096072_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP010833.1|WP_075263453.1|1082612_1083767_+|acyl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173851
NZ_CP010833.1|WP_075263458.1|1087940_1088807_+|DUF2236-domain-containing-protein	unknown	unknown	gnl|CDD|378343
NZ_CP010833.1|WP_075263464.1|1096845_1098000_+|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase	unknown	unknown	gnl|CDD|234825
NZ_CP010833.1|WP_075263465.1|1099311_1100139_+|RNA-polymerase-sigma-factor-SigF	unknown	unknown	gnl|CDD|274373
NZ_CP010833.1|WP_075268237.1|1098038_1099046_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|275033
NZ_CP010833.1|WP_010064026.1|1079493_1079691_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_079181415.1|1096068_1096731_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816
NZ_CP010833.1|WP_075263460.1|1090550_1092134_-|molybdopterin-dependent-oxidoreductase	unknown	unknown	gnl|CDD|239028
NZ_CP010833.1|WP_075263461.1|1092292_1094515_-|NADP-dependent-isocitrate-dehydrogenase	unknown	unknown	gnl|CDD|377178
NZ_CP010833.1|WP_075263448.1|1074394_1076719_-|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	unknown	unknown	gnl|CDD|235367
NZ_CP010833.1|WP_075263452.1|1081113_1082616_+|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|143404
NZ_CP010833.1|WP_079181599.1|1077129_1078524_-|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075263457.1|1086835_1087900_+|lipoate--protein-ligase-family-protein	unknown	unknown	gnl|CDD|223173

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075263450.1|1078586_1079234_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	3.45049e-09
NZ_CP010833.1|WP_075263451.1|1079701_1080571_-|precorrin-6A-synthase-(deacetylating)	gnl|CDD|236218	PRK08284, PRK08284, precorrin 6A synthase; Provisional.	6.21616e-145
NZ_CP010833.1|WP_075263454.1|1083763_1084831_+|enoyl-CoA-hydratase/isomerase-family-protein	gnl|CDD|235533	PRK05617, PRK05617, 3-hydroxyisobutyryl-CoA hydrolase; Provisional.	0
NZ_CP010833.1|WP_075263456.1|1085753_1086563_+|enoyl-CoA-hydratase	gnl|CDD|180295	PRK05862, PRK05862, enoyl-CoA hydratase; Provisional.	2.82368e-157
NZ_CP010833.1|WP_075263455.1|1084827_1085757_+|3-hydroxyisobutyrate-dehydrogenase	gnl|CDD|130753	TIGR01692, 3-hydroxyisobutyrate_dehydrogenase_mitochondrial, 3-hydroxyisobutyrate dehydrogenase. 3-hydroxyisobutyrate dehydrogenase is an enzyme that catalyzes the NAD+-dependent oxidation of 3-hydroxyisobutyrate to methylmalonate semialdehyde of the valine catabolism pathway. In Pseudomonas aeruginosa, 3-hydroxyisobutyrate dehydrogenase (mmsB) is co-induced with methylmalonate-semialdehyde dehydrogenase (mmsA) when grown on medium containing valine as the sole carbon source. The positive transcriptional regulator of this operon (mmsR) is located upstream of these genes and has been identified as a member of the XylS/AraC family of transcriptional regulators. 3-hydroxyisobutyrate dehydrogenase shares high sequence homology to the characterized 3-hydroxyisobutyrate dehydrogenase from rat liver with conservation of proposed NAD+ binding residues at the N-terminus (G-8,10,13,24 and D-31). This enzyme belongs to the 3-hydroxyacid dehydrogenase family, sharing a common evolutionary origin and enzymatic mechanism with 6-phosphogluconate. HIBADH exhibits sequence similarity to the NAD binding domain of 6-phosphogluconate dehydrogenase above trusted (pfam03446). [Energy metabolism, Amino acids and amines].	1.13878e-107
NZ_CP010833.1|WP_075263459.1|1088888_1090538_+|pentachlorophenol-monooxygenase	gnl|CDD|235728	PRK06184, PRK06184, hypothetical protein; Provisional.	8.96614e-101
NZ_CP010833.1|WP_075263462.1|1094647_1096072_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.7039e-56
NZ_CP010833.1|WP_075263453.1|1082612_1083767_+|acyl-CoA-dehydrogenase	gnl|CDD|173851	cd01162, IBD, Isobutyryl-CoA dehydrogenase. Isobutyryl-CoA dehydrogenase (IBD) catalyzes the alpha, beta- dehydrogenation of short branched chain acyl-CoA intermediates in valine catabolism. It is predicted to be a homotetramer.	0
NZ_CP010833.1|WP_079181415.1|1096068_1096731_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	5.07171e-82
NZ_CP010833.1|WP_075263464.1|1096845_1098000_+|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase	gnl|CDD|234825	PRK00726, murG, undecaprenyldiphospho-muramoylpentapeptide beta-N- acetylglucosaminyltransferase; Provisional.	1.82968e-114
NZ_CP010833.1|WP_075263465.1|1099311_1100139_+|RNA-polymerase-sigma-factor-SigF	gnl|CDD|274373	TIGR02980, SigBFG, RNA polymerase sigma-70 factor, sigma-B/F/G subfamily. This group of similar sigma-70 factors includes clades found in Bacilli (including the sporulation factors SigF:TIGR02885 and SigG:TIGR02850 as well as SigB:TIGR02941), and the high GC gram positive bacteria (Actinobacteria) where a variable number of them are found depending on the lineage.	2.03848e-107
NZ_CP010833.1|WP_075263458.1|1087940_1088807_+|DUF2236-domain-containing-protein	gnl|CDD|378343	pfam09995, DUF2236, Uncharacterized protein conserved in bacteria (DUF2236). This domain, found in various hypothetical bacterial proteins, has no known function. This family contains a highly conserved arginine and histidine that may be active site residues for an as yet unknown catalytic activity.	6.66261e-58
NZ_CP010833.1|WP_075268237.1|1098038_1099046_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|275033	TIGR04180, NAD-dependent_epimerase/dehydratase, NAD dependent epimerase/dehydratase, LLPSF_EDH_00030 family. This clade within the NAD dependent epimerase/dehydratase superfamily (pfam01370) is characterized by inclusion of its members within a cassette of seven distinctive enzymes. These include four genes homologous to the elements of the neuraminic (sialic) acid biosynthesis cluster (NeuABCD), an aminotransferase and a nucleotidyltransferase in addition to the epimerase/dehydratase. Together it is very likely that these enzymes direct the biosynthesis of a nine-carbon sugar analagous to CMP-neuraminic acid. These seven genes form the core of the cassette, although they are often accompanied by additional genes that may further modify the product sugar. Although this cassette is widely distributed in bacteria, the family nomenclature arises from the instance in Leptospira interrogans serovar Lai, str. 56601, where it appears as the 30th gene in the 91-gene lipopolysaccharide biosynthesis cluster.	5.79726e-163
NZ_CP010833.1|WP_075263460.1|1090550_1092134_-|molybdopterin-dependent-oxidoreductase	gnl|CDD|239028	cd02110, SO_family_Moco_dimer, Subgroup of sulfite oxidase (SO) family molybdopterin binding domains that contains conserved dimerization domain. This molybdopterin cofactor (Moco) binding domain is found in a variety of oxidoreductases, main members of this family are nitrate reductase (NR) and sulfite oxidase (SO). .	1.55699e-82
NZ_CP010833.1|WP_075263461.1|1092292_1094515_-|NADP-dependent-isocitrate-dehydrogenase	gnl|CDD|377178	pfam03971, IDH, Monomeric isocitrate dehydrogenase. NADP(+)-dependent isocitrate dehydrogenase (ICD) is an important enzyme of the intermediary metabolism, as it controls the carbon flux within the citric acid cycle and supplies the cell with 2-oxoglutarate EC:1.1.1.42 and NADPH for biosynthetic purposes.	0
NZ_CP010833.1|WP_075263448.1|1074394_1076719_-|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase	gnl|CDD|235367	PRK05222, PRK05222, 5-methyltetrahydropteroyltriglutamate--homocysteine S-methyltransferase; Provisional.	0
NZ_CP010833.1|WP_075263452.1|1081113_1082616_+|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase	gnl|CDD|143404	cd07085, ALDH_F6_MMSDH, Methylmalonate semialdehyde dehydrogenase and ALDH family members 6A1 and 6B2. Methylmalonate semialdehyde dehydrogenase (MMSDH, EC=1.2.1.27) [acylating] from Bacillus subtilis is involved in valine metabolism and catalyses the NAD+- and CoA-dependent oxidation of methylmalonate semialdehyde into propionyl-CoA. Mitochondrial human MMSDH ALDH6A1 and Arabidopsis MMSDH ALDH6B2 are also present in this CD.	0
NZ_CP010833.1|WP_079181599.1|1077129_1078524_-|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	9.61058e-47
NZ_CP010833.1|WP_075263457.1|1086835_1087900_+|lipoate--protein-ligase-family-protein	gnl|CDD|223173	COG0095, LplA, Lipoate-protein ligase A [Coenzyme metabolism].	1.10118e-59

Protein sequences

>NZ_CP010833.1|WP_075263456.1|1085753_1086563_+|enoyl-CoA-hydratase
MSEKNESAATSGPYSTILVERRGRTALLTLNRPKALNALSLDVMRETVEATEALDRDPDVGCIVITGSGEKAFAAGADIKEMQPQSYMDMYLSDWFTAWDRLGQLRTPTIAAVRGYALGGGCELAMLCDLVIASKSAVFGQPEIRLGVIPGIGGSQRLTRAVGKAKAMDLCLTGRNMDAEEAERAGLVSRIVPDADLLEEALAVAGTVSGMSAPVAMMAKEAVNRAFETTLAEGVRFERRLFHAVFATADQKEGMKAFTEKRPAEFTHR
>NZ_CP010833.1|WP_075263455.1|1084827_1085757_+|3-hydroxyisobutyrate-dehydrogenase
MTTTVAFIGLGHMGGPMAANLVRAGHRVLGHDLVESCLAAAVESGVEQAGNAAEAAAIADVVITMLPAGRHVLSLYGPEGLLAAARPGTLFIDCSTVDVADSRAAHAAASAAGHRSLDAPVSGGVVGAEAGTLAFMAGGEEAAFAEAEPLLTVMGKKAVHCGAAGAGQAAKICNNMILGVSMIAVSEAFVLAESLGLSDQALFDVASAASGQCWALTVNCPVPGPVPGSPANRDYRPGFAAPLMAKDLGLAANAVRAGGVDAELGLRAAELYARFAEGGGADQDFSGIVRAIRAASSTTAADTEKGATP
>NZ_CP010833.1|WP_075263454.1|1083763_1084831_+|enoyl-CoA-hydratase/isomerase-family-protein
MTGEHVLVHTEGRTGVVTLNRPKALNALTHPMVETIAAALDRWEHDPGVAAVVITGAGERGLCAGGDIRSIHEDARAGGKASVAFWRDEYRLNARIARYPKPYVAVMDGIVMGGGVGVSAHGSVRIVTERSKVAMPETGIGFVPDVGGTYLLALAPGELGTHLALTGAVVGARDALLCGLADHFVPADGLPAFLAALRTEPPAAVLHRHVREAPPGVLEDNRAWIDHCYAADTVEEIVERLLASDAPAAGEAAATILGRSPVALKVTLAALRRARELGPLERVLEQEYRVSCAALSSADLVEGIRAQVIDKDRDPHWTPGTLVEVTDADVARYFAPTGDEGLSLAVSDSPQEVPW
>NZ_CP010833.1|WP_075263453.1|1082612_1083767_+|acyl-CoA-dehydrogenase
MSTVTTLLTDDQFAVVETTLDFAQEHLAPHAVAWDQDKHFPVDVLRKAAGLGLGGVYVREDLGGSGLTRSDGVLVFEALATGCPSIAGYLSIHNMVGWMIDRYGTEDQRARYLPGLCTMEQLGSYCLTEPGAGSDAAALRTRAVRDGDHWVLTGTKQFISGAGASHLYIVLARTGEDGPRGISAFVVERDDPGLSFGANEKKMGWNAQPTRQVLMDGVRIPADRLLGEKGGGFRIAMNGLNGGRLGIAACSLGGAQSALDRSLAHLADREAFGGRLLDAQALQFRLADMATELAAARALVRQAAEALDRNTTGAPQLCAMAKHFATDTGYSVADRALQLHGGYGYLAEYGIEKIVRDLRVHQILEGTNEIMRVMVARSLTGALR
>NZ_CP010833.1|WP_075263452.1|1081113_1082616_+|CoA-acylating-methylmalonate-semialdehyde-dehydrogenase
MVRELTHFIGGKHTSGTSGGFGDVFDPNTGRVQARVPLADRAETEAAIADAVEAQREWGEWNPQRRARVLLRFLQLVEKEKDSLARLLSSEHGKTVADAHGDIARGLDVVEFAAGVPHLLKGEFSDNAGAGIDVHSLRRPLGVVAGITPFNFPAMIPLWKAAPALACGNAFILKPSERDPSVPLRLAELFLEAGLPPGVLNVVNGGKESVDTLLEDPRVKALGFVGSTPIAAHIYATAAAHGKRAQCFGGAKNHMIVMPDADLDQAVDALIGAGYGSAGERCMAISVAVPVGEATADALVARLTERIGELRIGRSDDPDADFGPLVGRDAVDRVRGYVDLGVEEGAELVVDGRDFTLEGHEDGFFAGASLFDRVTPDMRIYQEEIFGPVVCVVRAADYEEALRLPSEHPYGNGVALFTRDGDTARDFTRRVDTGMVGVNVPIPVPVAYHTFGGWKRSGFGDLNQHGPDAIRFYTRTKTVTSRWPASGIRDGASFTIPTMG
>NZ_CP010833.1|WP_075263451.1|1079701_1080571_-|precorrin-6A-synthase-(deacetylating)
MADAGEAPRHILVIGMGAGDPDHLTLAAVKAMRRADVFFVLGKGKEKESLTRLRRDILDEHLTGPYRVVEADDPWRDRTQDDATRYTSAVHDWRHRRADICEHLIIEELAPGQCGAFLVWGDPALYDSTLAILDDIRGRGTVEFGHEVIPGISSVSALAARHRVTLNQVGRPIHITPGRRLAQGFPEDDGDIVVMLDGHETFTHLTGRGLWIHWGAYIGTPDEILVSGPLDEVAGEISRVRAEARERHGWIMDTYLLRQGPRDEKAAAGEGAAGRPADGADGSVGGPLG
>NZ_CP010833.1|WP_010064026.1|1079493_1079691_+|hypothetical-protein
MKKTVGWAQDGDDWTITVNGTQYRAVERPTDGRVDNYLVRGDDLSAECPSLGHGLGVIREHESRR
>NZ_CP010833.1|WP_075263450.1|1078586_1079234_-|TetR/AcrR-family-transcriptional-regulator
MEDETPLRERLVDVGVEIVAAEGIAALGLREIARRAGVSHGAPRRYFPTHRSLLSAIAGRGFDALKGRLDTSLRPDGDPRAQVCLLADVYVGFAVEHRPMFELMFRHDLLDGGDEADGRPRLREKTLPLFASLVALVARHQQTGAARRPSPGPEPAPDVVAAALWANLHGIAQLWSWGSLSLTLDAPSPGDPHAHESLAPLIARTVDAHLGPANL
>NZ_CP010833.1|WP_079181599.1|1077129_1078524_-|MFS-transporter
MIVALDGSVLFVAQPSLQRDLSASLAQVQWTSTAYLLAVASLLVLAGRLGDRYGHTRLLLIGSLGFGAASAGIAVAPSVGWVIALRAVQGVCGALLQPATLALLRQVYPPDRLGPPVALRTSAIGAAAAAGPLLGGFLVEEFGWRSVFVINVPAALVIGLLCLAARVPAARGDRDASHRLEAGGALLLAVALALLVNALAGVELHGWADGRTVGGLLASSAAAAVLVRHQRRSHHPLVPAAVARSVPVTASMAMLLFTASGMFGALFVSTYFLQYALGLDPLDSVLRSLPLTAMMIVGAPVAGRLLRVLGARTTALGGVLLVVLGTGWLAGTGSGTGPVAMGAAFALLGAGYATVMVTATGTVVGDAPAGYAGVVGGLKQTAVNIGPVLGIAVAAGLLPAAGGVRAQQWEGSMGTAFLVLAAAAALALVPAALLPGARTGPPPGDTGRGRPERATPCLTSPSEV
>NZ_CP010833.1|WP_075263448.1|1074394_1076719_-|5-methyltetrahydropteroyltriglutamate---homocysteine-S-methyltransferase
MTAKPAAAAARATVYGYPRQGQNRELKKAVEGYWKGRVSADALRQTAADLRRETWQQLAEAGVHEVPTGDFSYYDHVLDTSVMVGAVPERHRDAVRADALDGYFAMARGTQDVAPLEMTKWFDTNYHYLVPELGPDTVFTADSAKQVAEFKEALALGHTPRPVLVGPVTYLLLAKAAPGVAADFEPLTLLDRLLPVYAEVLADLRAAGAEWVQLDEPALVQDRTSAELNAAARAYRDLGGLTDRPKLLVASYFGRLGEALAVLAKAPVDGLALDFTETGAGNLDDLAAAGGLPGKRLVAGVVNGRNIWINDFEKSLATLGTLLGLADRVDVSASCSLLHVPLDAKAERDIDPQIARWLAFARQKTEEIVVLARGLASGTDAITAELAANRADLASRTDAAITRDPAVRARTAAVTDADGRRSQPYAERTAAQRSHLGLPLLPTTTIGSFPQTTELRTARADLRAGRIDEAGYEERIRDEIREVLSFQEKAGIDVLVHGEPERNDMVQYFAEQLTGYLATQHGWVQSYGTRYVRPPVLAGDISRPEPMTVRWTAYAQSLTDRPVKGMLTGPVTMLAWSFVRDDQPLGETARQVALALRDEVNDLEANGTSVIQVDEPALRETLPLRAADHAAYLEWATESFRLATAGVRPDTQIHTHMCYAEFGDIVQAIDDLDADVISLEAARSHMQVARELAAHGYPREAGPGVYDIHSPRIPSTEEAAELLRKGLEAIPATRLWVNPDCGLKTRGWPETRASLENLVAAAREIRAELPTEAV
>NZ_CP010833.1|WP_075263457.1|1086835_1087900_+|lipoate--protein-ligase-family-protein
MHGEYKVPGGKLVVVDLDVEGGALRNVRVAGDFFLEPDEAILAIDAALEGAPATTDTAGLAARIEAALPDSTVMLGLSAEGVAIAVRRALARATEWSDYDWQLIHDAPQSPALHMALDEVITAEVAAGLRPPTLRVWEWDSPAVIIGSFQSLRNEVDPAGVERHGVDVVRRISGGGAMFAEPSSTITYSLAVPQALVSGLSFADSYAYLDDWVLEALADMGIKAWYQPLNDIATEVGKIAGAAQKRVVGPDGGPGAVLHHVTMAYDIDADKMLEVLRIGKEKMSDKGTRSAKKRVDPLRRQTGLPRQVVIERMIDSFRRRHGLTTGSVTDAELARAEELVRTKFATPEWTARVP
>NZ_CP010833.1|WP_075263458.1|1087940_1088807_+|DUF2236-domain-containing-protein
MDKTASGSGVRERLGRSLFARVAGPSGPENRARIHQTPGPRWFGPDRPVRRVHGDASMFIGGLRALLLQSLHPLAMAAVAGHSGFKGDPWGRLQRTSTFLAVTTFGTAEHAQEAVDRVRSVHERVRGTAPSGEPYHAADPHLLCWVHVAEVDSFLRAHQRYGARPLDGAGCDGYIHDMATVAHALGIPDPPHDRAELAERIAAYRPELRATREALDAARFILLHPPLPWPVRPPYAVLAANAVAALPPWAREPLRLPRVPGVEEICVRPAGKALTRTIRWAMTPPAGG
>NZ_CP010833.1|WP_075263459.1|1088888_1090538_+|pentachlorophenol-monooxygenase
MARSESTDVLVVGAGPVGLTLAAELRRAGVDCRIVDRLPARLPYAKAVGVQPRTLELFERMGLVREVLDAAVPMRGQLTYENGAERGRVELVLPPEVPYGFASLPQCDTERLLEEFLGRYGTGIERSTALVGFAQDPAGVTSRLTTTSGDEVEVRSRFLVGCDGAHSAVRKGLGLSFEGGAFPEEYMLADVEVGWDLPAGYGVRSMHRGEDGAIDDLLVCIPLPGNGRYRMSMLVPPELSAARQAESAGTTGGGDGVAHGLEGGTAPALPDIQKVLDRLAPEPVTASALRWSSVFRISHRLVDRYGEGRVFVAGDAAHIHPPTGAQGMNTGIQDACNLAWKLALAVEGAAGPQVLAGYDAERHPVGEEVVGRTVRHAAEGVQADPDDRETLLLREAQLLVGYRESPLVTPLAPDAPAPLRPGDRAPDCGGLTGDIAAHPVRLFEVLRGRGHVLLVYGDHPAGDPPLDLASAARELTGGRMETHRILPTVAPDRWTGIPHHHDSRGEFALQYGAGEGAAFVLRPDGYLTACLRPPTVGGLKGALGRVFLP
>NZ_CP010833.1|WP_075263460.1|1090550_1092134_-|molybdopterin-dependent-oxidoreductase
MRTVRINRTALTRNTLAALSGLLAGFAALTVAELVSAAVRPEASPVTAVGGAAIDRTPTGVKDWAIRTFGENDKIVLQLGIVATLALFAVAVGLLALRHRRTGSAAVLVFGAVGTAAAVSRPDSTGFTDGLPSLVGAVAGAILLYVLVGRLTRPRTVAGEEGESGWDRRGFLIAATAAAAASTAAGAVGRALNSRSAQDAIASRDAVRLPAPASAAKPIPAGAQPRVRGISSFTTPNDDFYRVDTALVIPKVDANTWRLRIHGKGVRRDLEFSYQDLLDRPLIEREITLCCVSNEVGGPYIGHARWIGVRLADLLKEAGVKPPSRGGEADQIVARSVDGMTLGTPVEDVMDGRDAMLAVGMNGEPLPFVNGFPVRMLVPGLYGYVSACKWIEDIELTTFDDYDAYWVKRNWAREAPIKTQSRIDTPKPFGRPEAGTVMVAGVAWAQHRGIEKVEIRVDDGPWKPAQLAEQATVDTWRQWTYPWKATPGSHTLTVRATDGTGETQTEKRTKTVPDGASGWHSVVVSVD
>NZ_CP010833.1|WP_075263461.1|1092292_1094515_-|NADP-dependent-isocitrate-dehydrogenase
MTDSTIIYTHTDEAPALATYSFLPVIEAYASTAGVTVERRDISLAGRIIASFPEHLKAEQRIDDALAELGELARTPGANIIKLPNISASIPQLKAAIAELQEQGYALPDYPDDPRTDADKDVRARYDKVKGSAVNPVLREGNSDRRAPASVKNYAKAHPHRMGAWTADSKTNVATMGVDDFRSTEKSAVVAEDGTLRIELHGDDGTTTVLRESVPVLKGEVVDAAVMRVAALREFFTAQVARAKAEGVLFSLHLKATMMKVSDPIIFGHAVRAFFPNTFAKYGEQLAAAGLTPNDGLGGILKGLGSLPDVGAEIQASFEAELAEGPALAMVDSDKGITNLHVPSDVIVDASMPAMIRTSGHMWGPDGDEADTIAVLPDSSYAGVYQVVIDDCRANGAFDPATMGSVPNVGLMAQKAEEYGSHDKTFEIPATGTVRVVDASGTVVLEQAVGAGDIFRMCQTKDLPIQDWVKLAVTRARATGNPAVFWLDETRAHDANLIAKVKTYLADHDTDGLDISVKSPEEATAFSLERIRRGEDTISVTGNVLRDYLTDLFPILELGTSAKMLSVVPLMNGGGLFETGAGGSAPKHVQQLVKENYLRWDSLGEFLALAVSFEHLATTTDNARAQVLADTLDRATGTFLNEDKSPSRRLGGIDNRGSHFYLALYWAQELAQQTDDAKLAEAFAPLAKTLAEQEETIVAELIAVQGSPAEIGGYFQPDPAKAAAVMRPSATFNNAIASLA
>NZ_CP010833.1|WP_075263462.1|1094647_1096072_-|HAMP-domain-containing-histidine-kinase
MSGVRRLGARWRRRRPLRTRLAVAASAAVALVAVGVCAAAFFVIRYELLHQLDLSLTQSATRVIQENRGEGPQTVAGECRYLSAPACAQIVPADPAADPDAAYLLPVATPVREVAAGKRAPYYSNVSRFGQPLRMLTTPFGDGRALQVALRADPVEKGVRQAAVLLTAVGGAGVLLAGLLGYAVSRTGLAPVARLTSTAERIAATRDPRHRIELPPGPPGRQDEVTRLAASFNTMLGELEQSVSSQRRLVADASHELRTPLTALRTNAELLARGDRLTPAQRERASGALGRGIREVTGLVNDLIELARDEEPLPLLEEVRIAEVAEHTVAVARTHWPQTPFLLEAGAGAAEAVRPGVPARLARLLTNLLDNAAKFSPPGTPVEVGLTTHGGGLELTVRDHGPGIPAEDVPYVFDRFYRAEAARALPGSGLGLAMARQIARAHGAELTAGAAPGGGALFTLTFGGQGPPGGSHAP
>NZ_CP010833.1|WP_079181415.1|1096068_1096731_-|response-regulator-transcription-factor
MAEDEPDVRAAVEDGLSVEGYEVRGVGDGLAALSAVAAWEPDALVLDVMMPALDGLAVCRRLRAMEDRTPVLVLTALSSVSERVDGLEAGADDYLVKPFALDELVARVRALLRRAAPPVPDGNLAFADLTLDPVTRTGRRGGRPVEFSRTEAALLELLLRHPGQVLAREVILERVWGQDFGPDSNSLAVYVGYLRRKLEAGGEPRLVHTVHGLGYRLDVA
>NZ_CP010833.1|WP_075263464.1|1096845_1098000_+|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase
MRTPLSVVIGAGGTGGHIYPGLALAEALRRADPDAVISFIGTERGLETTLIPAAGYRLHTVDMIPFDPALGAKRFLLPAALLRSGAQARSVLRTQKAQVVVGMGGYPSAPAIVGAKMAGLPSVIHESNAVPGRANQFAARLTEHLTVAFDGSRAHLSGGERARTVGMPIAASLAALDRPALREEARRAFGIPEGARVVLFNGGSLGAARLTAAAVGLAARWRGREDVHLLIKTGPAALAETRHKLIDAGAGPVAAQAVPYLDRMDLAYAVADLVVCRAGSATIAELATTGVPAVLVPYPYAPGDHQTHNARVLSDAGAAYLVPDAETTADRLAGLIDPLLADPARLAVMGRAAGPGHHARAADLLAETVIRLAGQPTTEREFTP
>NZ_CP010833.1|WP_075268237.1|1098038_1099046_+|NAD-dependent-epimerase/dehydratase-family-protein
MNSTAVDWTGRTVLVTGAEGFIGSTLVDLLVERGARVRAFVHYKPYADKGHLARYLDDPHGPVEFIAGDVGDAGRVMDAVEGCDTVFHLAALIGIPYSYDSPGAYVRTNVVGTENIAEACRRHSVRRLLHTSTSEVYGTALTAPIGEDHPLQPQSPYSASKIGADMMALSHWHAFELPVTVVRPFNTYGPRQSARAVIPAILAQLHSGAREIRLGSLTPTRDFTYVTDTAAGFLALADCDRALGESVNLGTGREISVGDLAKALIAASGRDAEIVVDPARLRPSGSEVHRLLSDNTRARTWAGWEPEVGLEEGLERTSAWVAEHLHLFAPGRYQV
>NZ_CP010833.1|WP_075263465.1|1099311_1100139_+|RNA-polymerase-sigma-factor-SigF
MPAAPAALPLIDDPGKIAPKDARKLAVLFFDQLQVLEEGTHEYQYARNTLIEMNLSLVHFAAKRFRNRGSGEMEDIIQVGTIGLIKAIDRFELSREVEFTSFAIPYIVGEIKRFFRDSTWAVHVPRRLQELRVTLAKTREALSTRLDREPTVAELAQHLELTEEEVIEGLIAANGYTAGSLDLPIGADQNSAETVTYGDIKGDVDPAMELVEDLHTLAPLLEQLDEREREIVAMRFGQEMTQAQIGEHLGISQMHVSRLLSRLLTKLRKDMLTEK

Crispr_ID: NZ_CP010833_7

• CRISPR_ID: NZ_CP010833_7
• CRISPR_location: 2052416-2052505
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_7

Consensus_repeat	Method
CAAGTCCAGCTACAGCAACGGTGACGGCGG	CRISPRCasFinder

spacers of NZ_CP010833_7

>7.1|2052446|30|NZ_CP010833|CRISPRCasFinder
GGCCTGCGTCGAAGTCGCCTACCACTGGCG

CRISPR arrays and Neighbor proteins around NZ_CP010833_7

CRISPR arrays

The CRISPR arrays of NZ_CP010833_7

>merge|NZ_CP010833|7|2052416-2052505|CRISPRCasFinder
CAAGTCCAGCTACAGCAACGGTGACGGCGGGGCCTGCGTCGAAGTCGCCTACCACTGGCGCAAGTCCAGTTACAGCAACGGTGACGGCGG

>NZ_CP010833|7|7|2052416-2052505|CRISPRCasFinder
CAAGTCCAGCTACAGCAACGGTGACGGCGG	GGCCTGCGTCGAAGTCGCCTACCACTGGCG
CAAGTCCAGTTACAGCAACGGTGACGGCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075264050.1|2056144_2056690_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264047.1|2054052_2055000_-|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224995
NZ_CP010833.1|WP_075264039.1|2045608_2045905_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264043.1|2049936_2050905_-|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|223566
NZ_CP010833.1|WP_075264044.1|2051001_2051415_-|ATP-binding-protein	unknown	unknown	gnl|CDD|340413
NZ_CP010833.1|WP_075264046.1|2053151_2054027_-|AraC-family-transcriptional-regulator	unknown	unknown	gnl|CDD|214874
NZ_CP010833.1|WP_075264053.1|2058621_2060004_-|hypothetical-protein	unknown	unknown	gnl|CDD|374433
NZ_CP010833.1|WP_006127822.1|2052716_2052959_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264042.1|2049231_2049837_-|deaminase	unknown	unknown	gnl|CDD|334719
NZ_CP010833.1|WP_075264054.1|2060062_2063164_-|glycosyl-hydrolase	unknown	unknown	gnl|CDD|224389
NZ_CP010833.1|WP_079181434.1|2045935_2046535_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|223532
NZ_CP010833.1|WP_006127827.1|2048773_2049040_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	unknown	unknown	gnl|CDD|182475
NZ_CP010833.1|WP_075264049.1|2055802_2056036_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264052.1|2057862_2058489_+|SMI1/KNR4-family-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264037.1|2042711_2043785_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	unknown	unknown	gnl|CDD|182464
NZ_CP010833.1|WP_075268290.1|2044642_2044984_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264038.1|2044052_2044631_+|hypothetical-protein	unknown	unknown	gnl|CDD|274926
NZ_CP010833.1|WP_075264041.1|2047113_2048637_-|catalase	unknown	unknown	gnl|CDD|163712
NZ_CP010833.1|WP_075264048.1|2055147_2055735_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_075264051.1|2056779_2057784_+|YdcF-family-protein	unknown	unknown	gnl|CDD|99750

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075264054.1|2060062_2063164_-|glycosyl-hydrolase	gnl|CDD|224389	COG1472, BglX, Beta-glucosidase-related glycosidases [Carbohydrate transport and metabolism].	2.60513e-78
NZ_CP010833.1|WP_075264038.1|2044052_2044631_+|hypothetical-protein	gnl|CDD|274926	TIGR04025, hypothetical_protein, PPOX class probable FMN-dependent enzyme, DR_2398 family. Members of the PPOX family (see pfam01243) may contain either FMN or F420 as cofactor. This subfamily consists of proteins mostly from species that lack the capability to synthesize F420, and therefore most likely all bind FMN.	3.60285e-82
NZ_CP010833.1|WP_075264043.1|2049936_2050905_-|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|223566	COG0492, TrxB, Thioredoxin reductase [Posttranslational modification, protein turnover, chaperones].	1.10671e-46
NZ_CP010833.1|WP_075264044.1|2051001_2051415_-|ATP-binding-protein	gnl|CDD|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	2.14816e-22
NZ_CP010833.1|WP_075264046.1|2053151_2054027_-|AraC-family-transcriptional-regulator	gnl|CDD|214874	smart00871, AraC_E_bind, Bacterial transcription activator, effector binding domain. This domain is found in the probable effector binding domain of a number of different bacterial transcription activators.and is also present in some DNA gyrase inhibitors. The absence of a HTH motif in the DNA gyrase inhibitors is thought to indicate the fact that these do not bind DNA.	2.3227e-27
NZ_CP010833.1|WP_075264042.1|2049231_2049837_-|deaminase	gnl|CDD|334719	pfam01872, RibD_C, RibD C-terminal domain. The function of this domain is not known, but it is thought to be involved in riboflavin biosynthesis. This domain is found in the C-terminus of RibD/RibG, in combination with pfam00383, as well as in isolation in some archaebacterial proteins. This family appears to be related to pfam00186.	8.83457e-21
NZ_CP010833.1|WP_079181434.1|2045935_2046535_-|GNAT-family-N-acetyltransferase	gnl|CDD|223532	COG0456, RimI, Acetyltransferases [General function prediction only].	2.17067e-07
NZ_CP010833.1|WP_075264048.1|2055147_2055735_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.03675e-12
NZ_CP010833.1|WP_006127827.1|2048773_2049040_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	gnl|CDD|182475	PRK10457, PRK10457, hypothetical protein; Provisional.	2.1845e-13
NZ_CP010833.1|WP_075264053.1|2058621_2060004_-|hypothetical-protein	gnl|CDD|374433	pfam16208, Keratin_2_head, Keratin type II head.	6.62655e-08
NZ_CP010833.1|WP_075264037.1|2042711_2043785_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit	gnl|CDD|182464	PRK10441, PRK10441, Fe(3+)-siderophore ABC transporter permease.	2.30832e-88
NZ_CP010833.1|WP_075264047.1|2054052_2055000_-|NAD(P)-dependent-oxidoreductase	gnl|CDD|224995	COG2084, MmsB, 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases [Lipid metabolism].	4.82992e-36
NZ_CP010833.1|WP_075264041.1|2047113_2048637_-|catalase	gnl|CDD|163712	cd08156, catalase_clade_3, Clade 3 of the heme-binding enzyme catalase. Catalase is a ubiquitous enzyme found in both prokaryotes and eukaryotes, which is involved in the protection of cells from the toxic effects of peroxides. It catalyzes the conversion of hydrogen peroxide to water and molecular oxygen. Catalases also utilize hydrogen peroxide to oxidize various substrates such as alcohol or phenols. Clade 3 catalases are the most abundant subfamily and are found in all three kingdoms of life; they have a relatively small subunit size of 43 to 75 kDa, and bind a protoheme IX (heme b) group buried deep inside the structure. Clade 3 catalases also bind NADPH as a second redox-active cofactor. They form tetramers, and in eukaryotic cells, catalases are located in peroxisomes.	0
NZ_CP010833.1|WP_075264051.1|2056779_2057784_+|YdcF-family-protein	gnl|CDD|99750	cd06259, YdcF-like, YdcF-like. YdcF-like is a large family of mainly bacterial proteins, with a few members found in fungi, plants, and archaea. Escherichia coli YdcF has been shown to bind S-adenosyl-L-methionine (AdoMet), but a biochemical function has not been idenitified. The family also includes Escherichia coli sanA and Salmonella typhimurium sfiX, which are involved in vancomycin resistance; sfiX may also be involved in murein synthesis.	3.13832e-42

Protein sequences

>NZ_CP010833.1|WP_075264044.1|2051001_2051415_-|ATP-binding-protein
MNETTQLPYFRAAFYCRERRSIPVVRKFARKALVEWECEQRADDVLLCVTELATNALRHGVPPGRGFKLHIYLERVESIIRVEMHDSGGGVVRAADGPPEADDEGGRGLLLVAALADKWGVAERNPGKIVWCEFSIV
>NZ_CP010833.1|WP_075264043.1|2049936_2050905_-|NAD(P)/FAD-dependent-oxidoreductase
MKQQRYDVVIVGGGAAGLSGALALGRARRSVLVIDAGEPRNAPASHVHNYLGRESTPPGELLAIGRSEAAGYGAEIVEGRVASAEKLPEDGGEQGFRVVTEGGRSVEARRLLVTTGLVDELPPVPGLAARWGREVLHCPYCHGHEVADRPIGVLATGPLAVHQALMWRQWSDDVALFLHTGPEPTEEEYEQLAARGVAVVDGEVTGLEVADDRFTGVTLASGRVVPREALVVQARFTARSAVLESLGLKPVAQEMGGVVIGTYIPTDPTGATEVPGVWAAGNVTRLTEQVIGAAAAGLMAAGAVNGDLIAEDTRLAVAARRA
>NZ_CP010833.1|WP_075264042.1|2049231_2049837_-|deaminase
MSELLVDFITSLDGYASGEGWPGFWGLEGPEYLAWLGEQPEVTHLMGANTYRLMSGFAAGEVPSGQDEFRPEEEASVDELTQAPKVVFSSSLEEPLAWANSTLVRGDAVEAVRAMKENGSGLLSTIGSLSLCRSLLRAGLVDRFRVVMFPVITGATGSERIYDGYPDVALEMIEHRTFDGRTQLVEYKPRVLEHPPLGAPA
>NZ_CP010833.1|WP_006127827.1|2048773_2049040_-|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein
MGIIAWILIGLLAGAIAKALMPGKDPGGCLITMLLGIAGGLLGGWLGKVIFGVDSIDGFFSLSTWIAAVVGSVILLALYRLIAGNRSR
>NZ_CP010833.1|WP_075264041.1|2047113_2048637_-|catalase
MTDTTRKPTTSDSGAPVESDEHSLTVGPGGPILLQDSYLIEQMAQFNRERIPERQPHAKGSGAFGKFEVTADVSAYTKAALFQPGTTTDLVVRFSTVAGERGSPDTWRDPRGFAVKFYTSEGNYDMVGNNTPVFFVKDPMKFQHFIRSQKRRADNNLRDHDMQWDFWTLSPESAHQVTWLMGDRGIPRTWRHMNGYTSHTYMWINAQGERFWVKYHFKTDQGVETFTQDEADQMAAADTDYHTRDLFEHIRDGDFPSWTLKVQIMPFEDAKDYRFNPFDLTKVWPHGDYPLIEVGRMTLDRNPTDNHAEIEQAAFQPNNFVPGIGPSPDRMLLARLFSYADAHRHRIGGNYQQLPVNAPVAPVHTYSKDGAMAYRKTSDPVYAPNSKGGPEADTARYGTPPSWYADGDITRAAYVDHAEDDDWGQAGTMVREVLDDAARDRLVDNVVGHLVNGVTEPILQRAFQYWSNIDAGIGKRIEEGVRAKAGEKDPKAGEQGNPARSSMQRKA
>NZ_CP010833.1|WP_079181434.1|2045935_2046535_-|GNAT-family-N-acetyltransferase
MPITNTPQAATLDDAPEVSRTLARAFADDPMMEWFFPGGASREPDLVRYFTTIFTRQYGRHGVCERTASAAAFWVAPEGQEKTVPDAETVAELEEILGDRASLFRDAVAAAAEQGPKEPHWYLAVVGADPAARGQGHGAALLRSGLAQADAAGLPVYLESSKPDNLPFYERFGFTVLGEARLPGGGPALWVMRREPRAV
>NZ_CP010833.1|WP_075264039.1|2045608_2045905_+|hypothetical-protein
MTEETILLRDFLATMNRLQAEFERRLDGIEQDAPPGPPPHAGSRAVADPWQPRGSHDLDRPLGLEAIWTEGRRSPVARADGSGARPWAEKAFFTAYPD
>NZ_CP010833.1|WP_075268290.1|2044642_2044984_-|hypothetical-protein
MGSLTFPLLWLALACVAGPLFGIAGAWSRRGTQPWRRYVALGALGGLFGSEGLHYWLGLGYAPQAVACGALACGLPLLLGRTWKERGLSLAVAAPASFFTYQVLYGVLNAVSG
>NZ_CP010833.1|WP_075264038.1|2044052_2044631_+|hypothetical-protein
MSYAADPTAPATDPLAGAVPLGSADELRELLGTPHPIVIDKVHDRLTDDDLALLARSPFCTLATSDADGNCDATPRGDTPGFTHVLDRGTIALPDRPGNRRADSFHNILSNPRVGLLYLIPGAMDVLRVNGRARILTDAPFFDAMTLRGQRPKLALVVEIDEIFRHCPASLKRSGVWAPETWAGAEPRVGGE
>NZ_CP010833.1|WP_075264037.1|2042711_2043785_-|iron-chelate-uptake-ABC-transporter-family-permease-subunit
MSGSTLLAKGEETPADGGREARRKRSRPVLALGLLAALAVLFLTAVASLAIGSGDVPFRDVVDGVLDPDTAVKGQLIVQEVRIPRTVAGLLAGAALGLAGTVMQGVARNPLADPQLLGINAGASVAVVCSITLLGFTVATQFIWFGFLGALLAALLVYGVGSLGREGATPVKLALAGAATAAVLTSVTSAILLQDRGSYDQFRFWQLGALTARSSEVLWQVSPFILVGTVLALALGPQLNALSLGDDLARGLGQRVGAIRMVSALAVVILCGAATVVAGPIGFVGLAVPHAARLITGPDYRWVLPYSMVLAPVMLLVADIVGRVVARPGEVQVGVITAAIGCIPFIWLVRRRKLVEL
>NZ_CP010833.1|WP_006127822.1|2052716_2052959_-|hypothetical-protein
MHRRIAALAVTVATAGAMLLGTASTASATGPGFWLRSHHASLAECQAVGNAGADNGLWSRVFICNPFAGKPGVYELWIRY
>NZ_CP010833.1|WP_075264046.1|2053151_2054027_-|AraC-family-transcriptional-regulator
MLERLNDAMEHIEAHLGERIEAADLARIAMTSEYHFRRMFSALAGLPLSEYIRRRRMTVAGAEVLGVRDRSLLDVATRYGYDTGEGFARAFRAVHGIGPGEARRTGAALRSQQRLTFRLVVEGSSAMRYSLVEKNAFRVVGRKARVPLIHEGPNPAIAEFIRGIGREELDRIAALSDQEPAGIVGVSDQLDPSRAEGTELDYWHGVVTGEAEPPEDLDALEVPAGTWAVFESEGEFPQALQYLWRDVFTQWFPSNPYASRPGPEILRVRLTEDGKRAEAELWIPVERSAES
>NZ_CP010833.1|WP_075264047.1|2054052_2055000_-|NAD(P)-dependent-oxidoreductase
MNSTATKRPGSVTVMGLGPMGRAMAGALLDRGYGVTVWNRTASRADGLVARGAVLAPTPADAVAANEVVILSLTDYVAVDAVLESAAQALNGRVLVNLTSATPEEARAGARRAAERGAVQLTGGVASPPSGIGQPDSATFYSGQREAFDRHRPVLETLTGRVEHQGEDPGLAALSYQLGMVMFWTSMLSFWQAVALARANGLKAADILPHATDTANSLAQFFGFYAERIDAGVHAGDVDRLAMGVASVEHVLHTHTEAGVDTTLPAAVVDLFRQGMEAGHAEESFSSLVGLLAKPGDPTGPGTDGRVREDGLSLR
>NZ_CP010833.1|WP_075264048.1|2055147_2055735_+|TetR/AcrR-family-transcriptional-regulator
MQTSTRDRIVVATARLLQRQGYVGTGIKQIAKESQATLGSIYHFFPGGKEAVAVAAIRHGDQEFAALLKDALDSEPDPAEAVFSCTRRLAAELKESGWVDGCPVTAAALETLGADSELQKACADALNGWERLVLDKLLGCGFPADDARELATTVISAIEGAEVTAQVNRSEEPLLAAGRQLARLIRSYGTETARR
>NZ_CP010833.1|WP_075264049.1|2055802_2056036_-|hypothetical-protein
MKKRSVLAAVTLATGAVIAAIAPHPGGADSAHAAEPAVSLGALDEVGDLGTLVDGAAGATTSTAGTVTSTVEGAKLS
>NZ_CP010833.1|WP_075264050.1|2056144_2056690_-|hypothetical-protein
MRWSFTLHGGAAAVLSAAALALAGLTWLPGRGALPLFEPAWPMAVVIIPAFLLFLAALVRQFATGADRSAQWQAFRCLPGRVQAGLGLLAVTSVAVMVIGAVAGAGERLQDAEVREGRYVAYDTSVTTDRAVELTQDEYLALLPSSRRMMFAVPGLLGAAAAAIVLAAGELRRADDASAAR
>NZ_CP010833.1|WP_075264051.1|2056779_2057784_+|YdcF-family-protein
MLAFAPAALLFLVFCVSALLERRKFSNAVVLGLAVLCALGALLYRLVSSESPSVPYVVGALVALGAMALLVLVCFLFLNGVRMLRKEGRSPSNLLSLLAALAILGVVALLATAAAVRTPVLIGLATAAGGLTLYFAFLFLCFVCYAFLYGRLRVRRKADFVVVLGSGLIGGTTVPPLLASRLKRGQTVHARLAKRGGSPVLITSGGQGPDEKLPESHAMADHLVAHGFPAELIEREDRSTNTEENLRFSKAIMEKAKPDYRCVVVTNNYHAFRAALTARRVGIRGQVVGSPTAAYFWPNAMLREFTAILVDYRQSNAAMCVIIVLGGVAAWYAS
>NZ_CP010833.1|WP_075264052.1|2057862_2058489_+|SMI1/KNR4-family-protein
MIGVTETTEPEENEVAAAPTTPEEWRVFLERYGELYVKVRADEEELVDLLDEDQLDALDQGERVEAWLGEAPAREEALAASEERLGVRFPAGLRGFFLASDGWTRLDGWVDGVHPCDRVVWMRDSEAGESVIEVYASIPGNEEVVELFRRSIEIARGEDFWLLDPTDVGPDGEWAAYEFTPKYGDTTKYPSFSALFHSGFESMEEDED
>NZ_CP010833.1|WP_075264053.1|2058621_2060004_-|hypothetical-protein
MRKRLFPALLAGLLLILAAAALALTSPASAAPAAKIQDAAQALRDDPVYVDPGARDQLSVADEKALENKITDADKPVFVAVFPDTSAFPEEGLLQTLRSDTGITGVYAIRLGDGFDAGADPQVMPTRAVENLTAAVENPTTAGNADTQLNAFVDRAVEQARGTAPASWSGGGGAADESGAPVGGLITLGALVAAGGAGAYAISRRNKRRKEEEERVALDKLRVVVDEDITAYGETLERLDFHPAEKGADDTMRADYERALDSYESAKTKMDKATHPSDVRGVTQSLEDGRYSLAVLEARRTGGQIPARRPPCFFDPRHGPSIADVLWTPSGGAAREVPVCGADEIRLSRGEDPMSRTVDTGDGNRRPYWEAGPAYGPWAGGYFGGGLLPGLLVGTMLGSMLATPAYASEYGGGDFGDGGAGGDWGGGDFSGSDFDSSGFGGGGFGDGGGFGGGGFDGGGF
>NZ_CP010833.1|WP_075264054.1|2060062_2063164_-|glycosyl-hydrolase
MPRIPYTRPRKGRSRPATAAFAAAAVLATLLAGSATGPAAAADEPAPVLIDRFEGEVPLGNNPPADAIFTWGGDADDHPQLKLARRADAPEGEQVLEGSYDISAYGGFSHEFAVDTPPQNWTAHKGIRFWWYGQNTAPLPPGSGKRVNFEIKDGGANGGASELWTTSFTDDWEGWHLVEIPFADFVYRADYQPVGGIDQVLGLNEMWGYALTLPGGAPGEFALDAVELYGKAEPALTASVVTDTAVRPVKNGATAELTLSVATTGSVPTEEPVTVTYATKGGTAEAGKDYTPVTGSHTFPAGTASGTTHKVTVRTAKASKPAEAKTIPLELTVTGAKAPRENPQVVIDAHGLPYQNAKLPVKQRVADLLGRLSLAEKAGQMTQAERNALRAPGDIAAYDLGSLLSGGGSVPTPNTAAAWAKMVDAYQLRAQATRFQIPLIYGVDAVHGHNNVVGATIMPHNIGIGAGRDPKSAEKTGAITAKEVRSTGVPWDFAPCVCVTRDERWGRSYEAFGEDPALVEAMETVIQGMQGSPSGKDLHRNDKVLGSAKHFVGDGGTEFGSSTTGSYTTDQGVTKVTREELEAVHLSPFEESVKRGVGTIMPSYSSLDILGDDQGPVKMHANAEMINGVLKDRMGFEGFVISDWQAIDQIPGDYPSDVRTSVNAGLDMIMVPTAYQDFTKTLKDEVTAGRISETRIDDAVARILTQKFRLGLFEKPYADTTHLDKVGSAEHRAVAREAAAKSQVLLKNDGAVLPLKPNQKVYVAGSNADDIGNQAGGWTISWQGSSGKTTTGTTILEGMKKAAKNPESVTYSRDASAATDGHDVGVVVVGETPYAEGIGDVGNGHDLELTAADKAAVDKVCAAMKCAVLIVSGRPQLIGDQLGDMDALVASWLPGSEGDGVADVLYGKRAFTGQLPVTWPKSEAQLPINVGDGTYDPQFPYGWGLTTLKKPPAGGELTLTALAVAAQIAEKAKLGKTPAGKAIVDQARLLVQQKIDGKFGQAVAKPFAEADHLLLKGDLTGAVAKLRTAYRAA

Crispr_ID: NZ_CP010833_8

• CRISPR_ID: NZ_CP010833_8
• CRISPR_location: 3350060-3350149
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_8

Consensus_repeat	Method
CTACAGCGGCAGCGAGGGCGGCGACTGCGT	CRISPRCasFinder

spacers of NZ_CP010833_8

>8.1|3350090|30|NZ_CP010833|CRISPRCasFinder
AGAGGTGGCGCTCACCTGGTCCAAGTCCAC

CRISPR arrays and Neighbor proteins around NZ_CP010833_8

CRISPR arrays

The CRISPR arrays of NZ_CP010833_8

>merge|NZ_CP010833|8|3350060-3350149|CRISPRCasFinder
CTACAGCGGCAGCGAGGGCGGCGACTGCGTAGAGGTGGCGCTCACCTGGTCCAAGTCCACCTACAGCGGCAGCCAGGGCGGCGACTGCGT

>NZ_CP010833|8|8|3350060-3350149|CRISPRCasFinder
CTACAGCGGCAGCGAGGGCGGCGACTGCGT	AGAGGTGGCGCTCACCTGGTCCAAGTCCAC
CTACAGCGGCAGCCAGGGCGGCGACTGCGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_079181463.1|3349203_3350031_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379262
NZ_CP010833.1|WP_075264902.1|3356116_3357571_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379258
NZ_CP010833.1|WP_075264896.1|3351883_3352504_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264890.1|3346152_3347055_-|CPBP-family-intramembrane-metalloprotease	unknown	unknown	gnl|CDD|376806
NZ_CP010833.1|WP_075264888.1|3345170_3345770_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_075264897.1|3352612_3353083_+|pyridoxamine-5'-phosphate-oxidase	unknown	unknown	gnl|CDD|132706
NZ_CP010833.1|WP_075264889.1|3345797_3346136_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264900.1|3354376_3355246_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|379262
NZ_CP010833.1|WP_075264894.1|3350263_3351196_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_CP010833.1|WP_107472797.1|3357644_3358565_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264899.1|3353680_3354109_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_032784107.1|3347492_3348278_+|methyltransferase	unknown	unknown	gnl|CDD|252734
NZ_CP010833.1|WP_075264887.1|3342726_3345012_-|beta-glucosidase	unknown	unknown	gnl|CDD|185053
NZ_CP010833.1|WP_075264901.1|3355220_3356027_+|S-adenosyl-methyltransferase	unknown	unknown	gnl|CDD|252734
NZ_CP010833.1|WP_075264895.1|3351310_3351838_+|sugar-O-acetyltransferase	unknown	unknown	gnl|CDD|100047
NZ_CP010833.1|WP_075264898.1|3353107_3353626_-|proline-dehydrogenase	unknown	unknown	unknown
NZ_CP010833.1|WP_075264886.1|3341910_3342633_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075264885.1|3340749_3341718_+|EamA-family-transporter	unknown	unknown	gnl|CDD|273359
NZ_CP010833.1|WP_075264891.1|3348413_3348608_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075268380.1|3348686_3349121_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_079181463.1|3349203_3350031_+|helix-turn-helix-domain-containing-protein	gnl|CDD|379262	pfam13560, HTH_31, Helix-turn-helix domain. This domain is a helix-turn-helix domain that probably binds to DNA.	5.98781e-08
NZ_CP010833.1|WP_075264902.1|3356116_3357571_+|helix-turn-helix-domain-containing-protein	gnl|CDD|379258	pfam13556, HTH_30, PucR C-terminal helix-turn-helix domain. This helix-turn-helix domain is often found at the C-terminus of PucR-like transcriptional regulators such as Bacillus subtilis pucR and is likely to be DNA-binding.	3.68165e-09
NZ_CP010833.1|WP_075264890.1|3346152_3347055_-|CPBP-family-intramembrane-metalloprotease	gnl|CDD|376806	pfam02517, Abi, CAAX protease self-immunity. Members of this family are probably proteases (after a isoprenyl group is attached to the Cys residue in the C-terminal CAAX motif of a protein to attach it to the membrane, the AAX tripeptide being removed by one of the CAAX prenyl proteases). The family contains the CAAX prenyl protease. The proteins contain a highly conserved Glu-Glu motif at the amino end of the alignment. The alignment also contains two histidine residues that may be involved in zinc binding. While they are involved in membrane anchoring of proteins in eukaryotes, little is known about their function in prokaryotes. In some known bacteriocin loci, Abi genes have been found downstream of bacteriocin structural genes where they are probably involved in self-immunity. Investigation of the bacteriocin-like loci in the Gram positive bacteria locus from Lactobacillus sakei 23K confirmed that the bacteriocin-like genes (sak23Kalphabeta) exhibited antimicrobial activity when expressed in a heterologous host and that the associated Abi gene (sak23Ki) conferred immunity against the cognate bacteriocin. Interestingly, the immunity genes from three similar systems conferred a high degree of cross-immunity against each other's bacteriocins, suggesting the recognition of a common receptor. Site-directed mutagenesis demonstrated that the conserved motifs constituting the putative proteolytic active site of the Abi proteins are essential for the immunity function of Sak23Ki - thus a new concept in self-immunity.	3.63425e-12
NZ_CP010833.1|WP_075264888.1|3345170_3345770_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.25339e-12
NZ_CP010833.1|WP_075264897.1|3352612_3353083_+|pyridoxamine-5'-phosphate-oxidase	gnl|CDD|132706	TIGR03667, Rv3369, PPOX class probable F420-dependent enzyme, Rv3369 family. A Genome Properties metabolic reconstruction for F420 biosynthesis shows that slightly over 10 percent of all prokaryotes with fully sequenced genomes, including about two thirds of the Actinomycetales, make F420. A variant of the Partial Phylogenetic Profiling algorithm, SIMBAL, shows that this protein likely binds F420 in a cleft similar to that in which the homologous enzyme pyridoxamine phosphate oxidase (PPOX) binds FMN. [Unknown function, Enzymes of unknown specificity].	3.6787e-07
NZ_CP010833.1|WP_075264900.1|3354376_3355246_+|helix-turn-helix-domain-containing-protein	gnl|CDD|379262	pfam13560, HTH_31, Helix-turn-helix domain. This domain is a helix-turn-helix domain that probably binds to DNA.	1.08449e-07
NZ_CP010833.1|WP_075264894.1|3350263_3351196_-|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	3.94064e-31
NZ_CP010833.1|WP_032784107.1|3347492_3348278_+|methyltransferase	gnl|CDD|252734	pfam04672, Methyltransf_19, S-adenosyl methyltransferase. This family contains a SAM (S-adenosyl methyltransferase) domain, with a central beta sheet with 3 alpha-helices on both sides. Crystal packing analysis of the structure Structure 3giw suggests that a monomer is the solution state oligomeric form. An unidentified ligand (UNL, cyan) was found at the putative active site surrounded by the residues His57, His170, Phe171, Tyr216 and Met22. The UNL is likely to be a phenylalanine or phenylalanine-like molecule. (details derived from TOPSAN).	2.04674e-117
NZ_CP010833.1|WP_075264887.1|3342726_3345012_-|beta-glucosidase	gnl|CDD|185053	PRK15098, PRK15098, beta-glucosidase BglX.	7.07216e-159
NZ_CP010833.1|WP_075264901.1|3355220_3356027_+|S-adenosyl-methyltransferase	gnl|CDD|252734	pfam04672, Methyltransf_19, S-adenosyl methyltransferase. This family contains a SAM (S-adenosyl methyltransferase) domain, with a central beta sheet with 3 alpha-helices on both sides. Crystal packing analysis of the structure Structure 3giw suggests that a monomer is the solution state oligomeric form. An unidentified ligand (UNL, cyan) was found at the putative active site surrounded by the residues His57, His170, Phe171, Tyr216 and Met22. The UNL is likely to be a phenylalanine or phenylalanine-like molecule. (details derived from TOPSAN).	8.3807e-113
NZ_CP010833.1|WP_075264895.1|3351310_3351838_+|sugar-O-acetyltransferase	gnl|CDD|100047	cd03357, LbH_MAT_GAT, Maltose O-acetyltransferase (MAT) and Galactoside O-acetyltransferase (GAT): MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively at the C6 position of the nonreducing end glucosyl moiety. GAT specifically acetylates galactopyranosides. Furthermore, MAT shows higher affinity toward artificial substrates containing an alkyl or hydrophobic chain as well as a glucosyl unit. Active MAT and GAT are homotrimers, with each subunit consisting of an N-terminal alpha-helical region and a C-terminal left-handed parallel alpha-helix (LbH) subdomain with 6 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X).	2.52998e-72
NZ_CP010833.1|WP_075264885.1|3340749_3341718_+|EamA-family-transporter	gnl|CDD|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	6.97796e-41

Protein sequences

>NZ_CP010833.1|WP_079181463.1|3349203_3350031_+|helix-turn-helix-domain-containing-protein
MHSSDQPESTAEMFGLLLRHFRVLAGLSQDQLGKRIGYSKSQVAMVERGARPPTDIFVQRADEVLRAQGALIVAAPKPPKQTERRNPLPGWFTPFADEEEKAWARHSYENQVIPGLLQTEAYAQAVFASHYPTYDDDEIEAKVAARLERQKLLSRRPLADISFVLEMIVLTRPIGGRRVMKAQLHHLAEVARLRHVRIQLMDPDREDHAALDGPFVLLETDKRQQLAYIEGQGGSFFVTEQPELGDLFGQYGVTRAQAYTPERTLEKIEKMAEEL
>NZ_CP010833.1|WP_075268380.1|3348686_3349121_-|hypothetical-protein
MELKNSPDPVPYCPSWIPASGHALRHVGIHFDAVRAIGLLGEEIAYEVMQFTDFQAGPIVRSGIGERSMYFLLAPGSAADHRWPPGVEAMSRSARGDAFVGVPALGGGTWPLDWRSRPTAEDPFVDSALLHEMAWLRAGCTVKE
>NZ_CP010833.1|WP_075264891.1|3348413_3348608_+|hypothetical-protein
MAHRISALISAFGVFASVLLLALAVREYRSGATVLWLVFGAAAFLGAVYALVVDVRRLRTEPTA
>NZ_CP010833.1|WP_032784107.1|3347492_3348278_+|methyltransferase
MTAQAPHPPIDTSKPHSARVYDALLGGKDNYPVDQQVAELLPVEAKIGAHQQRAFMHRATAWLAGQGVTQFLDIGTGIPTEPNLHQIAQEIRPSARIVYCDNDPIVLRHAEALLVSRPDGVTDYVHADVREPAIILDAARETLDFDRPIALSVLGLLHFLPDTEKPIDILRTFTDAMAPGSYVVLSHGASDVNEEKGEQSADEYKKGGIQLALRTREEFSRFFEGLEIVTPGLVKAPEWFNGTPAPEQEHSGMYVAVARVP
>NZ_CP010833.1|WP_075264890.1|3346152_3347055_-|CPBP-family-intramembrane-metalloprotease
MRAPSGSRYDEQGRNGQGGRFGWIGELSAVVGLVVAGVLVVSIGGFVLAELLDAGPADADSDLFFEDPVADLVVQLLGIAIAIPIVLWGARVIGRRPAGTVSSVVGRLRWGWLGRCAAVGFPLMVVQIGVLIAWTWNDEPVGESGSGFPGWPVFLLSLAVILALVPFQAAAEEYVFRGWLVQVIGRVVRTPWPAVVVASLLFALAHGFGELSGFLLLLYSALWWGWLVIRTGGLEAVIVMHVANNLLAFGLAAGFGELASTETAADAPWQAMVAELVFAPLYCLTVARIAGRRGIERVSP
>NZ_CP010833.1|WP_075264889.1|3345797_3346136_-|hypothetical-protein
MKGARLWKSCVPVAANLLLGIPAIVPAFLIWYVLSNGPLAELGWTRREPTENDGMWLWLVFVVPVVACFGGLWILLNLWMRRRLSAAVPPGPYWSLALVLTLSPYLLGVAFG
>NZ_CP010833.1|WP_075264888.1|3345170_3345770_+|TetR/AcrR-family-transcriptional-regulator
MTPGTRRGYAKGRAKRTEILDQAMTLFGEAGYRGASLRVIATRCGISHPGLLHHFPTKEALLLAVLQRRDDVDDEWLALGVTRGVDHLRRLVDLAELNAKRRGIVELFSVVAAEATAPDHPAHAYFEARYRTSVANTERAYLQAREAGELRDDVDPSAAGQQLIALMDGLQIQWLISDCTTDMAGVLRAHVRAQLTVDF
>NZ_CP010833.1|WP_075264887.1|3342726_3345012_-|beta-glucosidase
MGPKPPYLDPALPVVERVADLLGRMTLPEKVGQMLQLNAKEGVRHLVEDLHAGSILHASPERVREAAELTARTRLRIPLLVAEDCIHGHSFWEGATIYPTQLGMAATWDPELVERIARATAVEVAATGVHWTFSPVLCITRDLRWGRVSETFGEDPFLIGELASAMVRGYQGEGLDDPTAILACAKHFAGYSETQGGRDASEADISRRKLRSWFLPPFERVAKEGCRTFMLGYQSMDGVPITVNNWLLNEVLRGEWGYTGTLVTDWDNVGRMVWEQKVYADYAQASAAAVRAGNDMVMTTSNFFEGAQEAVAQGSLKEAEIDAAVRRILTLKFELGLFENPRHPDAGRQAEVIGSGAHAALNLEAARRSLVLLTNDGTLPFAGGLEAGGEGRRAVGPGPRTVAVIGPNADDAQTQLGDWAGSSGQADWLPDGQPRAMIRTVLDGFRDQVPADWAVSYAPGARILEVGPDPEGEFFPDGQPRPEVVHPASPDAELIAEAVAAAEAADHVVAVVGDRIELIGEGKSTATLELVGDQVALLDALAATGKPLVVVVISSKPLVLPPSALGAAAIVYAANPGMLGGRAIAELLLGLIEPTGRLPLSFARHAGQQPTYYNQVRGQHGTRYADLTQRPAFAFGEGLSYSTVAYTDLEVPTAVVDESETVRARVTVTNTGARPALETVQVYVSDTVTSVTWAEKELKAYRQVALAPGESREILFELPVADCTLVDAEGVRTVEPGRFELLVGPSSRDEALLRGEFTVKG
>NZ_CP010833.1|WP_075264886.1|3341910_3342633_+|hypothetical-protein
MRISKNLIGLAAVGILVAGCGSSSGDDSARTSASAGSAGKAPSEEAKAPEPGADLAVPVTGPQADVVASSSDPKLKVLPKPANGASFTEKVEHKLQEDLLGRLKVPGKTSANCPDGVTQKASAVSICNVTYEGATVPYEIEISEKYKPGSFLTFYNSTPKQGLLVAKNAYDRLWTSHKGRTDISKLSCEELPAAKAVDEETETGFHCQYWGKYAGEDRKGGFVKLGIKVNRHNVDFFEVR
>NZ_CP010833.1|WP_075264885.1|3340749_3341718_+|EamA-family-transporter
MEGNARWALTTAVAPVAWGATYFVTREFLPAGNPLYGAAIRALPAGLLLLAVCRKLPHGNWWVKSLILGALNMSGFFALVYVAAQRLPTSMASIIMAVAPLAMMLLAWGLVGERPGPRHLAGAGAGIAGVCLMVFTATGPVDPLGILASVAAMAVSSFGYVLAKRWSGEVDVLASTGWQLTGGGLLLLPFAALTEGAPPSLDGPALLGFAYVTVVATAFAFAVWFAGLARLPAGTVGLLGLLNPVTGVLLGVLIADETLSGRQICGLLLTLCGVLLGRQTARPRRTPDRNGGRAAGRATGPAGDRDVVECARGDGRSGHSRK
>NZ_CP010833.1|WP_075264894.1|3350263_3351196_-|LysR-family-transcriptional-regulator
MDAEALRTFVTVAETGQFQAAADELGISQQAVSKRIAALERHLGVMLLVRTSRGSRPSPDGQVFLPHAKRILAVVEQAEQAVRPGSRPLRVDVLNRRISPAQAVHRFYRSHPEMELDVVTLSTENAAQAARAVLEGTVDASFRALPADQVPAGISAERLMDAPLELLVGPGHPLADAPHVRPAELAGHRIWIPGIMPGTEWAAFYRTLSEAFGLSIDALGPDFGPEALMDTLADSDSLATLVGRGDRYLWPQAHDLRRIPLRDPTPVYPHVLLFRSGDQHPVLTALRDYLRTAGPRTPQDVWAPEWVETA
>NZ_CP010833.1|WP_075264895.1|3351310_3351838_+|sugar-O-acetyltransferase
MHVQTPEFARHAQRIVEVTDATSRLNALPFSDTEGRAELLSVVFGGPLPPSVTIYPPFFTEYGLNTTFGENVFVNQGCTFMDKGGIRIGNGVMIAPKVSLITGGHPLPLAERREFLSFAPIVIEDDVWIGTAAVITQGVTIGAGAVVAAGAVVTRDVPAGTVVAGVPARVVKTID
>NZ_CP010833.1|WP_075264896.1|3351883_3352504_-|hypothetical-protein
MGTDISGFIEYRAPGDDQEPVWFGAHDLSPLNDDVRNYDAFGCLFGVRNYANFRPLAADRGFPSDASGELSARFAQLAEWYGEDGFHSATWITWAEVNAVDWDEPAEKPDSRLHQYRQTPSGLRMTGKASWSAEFAEAVGLERGDVREWPEGAEWLIGDTLYRSVTLRRRDAVTETGEWRPVWEAMRSLAEQHGDDNVRLVVWFDD
>NZ_CP010833.1|WP_075264897.1|3352612_3353083_+|pyridoxamine-5'-phosphate-oxidase
MTAVGSPPHGPRSPEQRKREALERLVRDNDVWVATADATGEPCLVPLAFWWDGEAVWLATRDTNPTGRNLCSSGRARLSFGHTRDVVLVHGTARMLTREELPTEVGDAFAAKDGWDPRKDHPSYVFFRVTPQVLQAWGTVPEMAGRTLMRDGKWLV
>NZ_CP010833.1|WP_075264898.1|3353107_3353626_-|proline-dehydrogenase
MDSGLAALLGAAVGSAATLGAAIVSGRAQARSQHAQQSRQHRRDAYTRYLSALHDRDLAMDAVLDALRPDRPDLTAVEERTARFVTLAREVHRTCEVVILEGPATVAAVAERVTNASADLSYVMRTMADDARVGDTSRKAERSALAAERERVLYEAVKEFRLAARAAIGQAV
>NZ_CP010833.1|WP_075264899.1|3353680_3354109_-|hypothetical-protein
MNHPTGLTDPTPLNRLADVTPLVHPKLRSVVTAPRPAQPRPLDLRVRAQRIQIDELVVDDPHQVLAHARQAALDDPETAEQLGYSTTEPLPLPDAAALLCALYDTDVLTAMGLRLTRHTTRVSASNQQTEPVSLVRSTTPED
>NZ_CP010833.1|WP_075264900.1|3354376_3355246_+|helix-turn-helix-domain-containing-protein
MARERSGRTARHLVLVARLRHLREGAGLSVPQAATQLGWHPSTLRRLEQAQTSLDVGQVSALLALYGAGAAETDDIMGRLNAANMPGWWHPWRDAMAPWLMDLMSVESAASVVRTWHPALVPLLLRTPAYAMAVDEVMFPEREAAERQRRADFLVERQNRLQEQQTRLWAVLPVTALRCRVGDDEVMREQVRALQQTAERGDVTMQLHPEYAPPHPLTGVPALSLYRVEIREIADHVVREGGLPGTAEVWDSPHPVQTYQGMLDVSCVMAIRPARTREVLQDEYDRKWA
>NZ_CP010833.1|WP_075264901.1|3355220_3356027_+|S-adenosyl-methyltransferase
MSTTGNGPELPAQIDTSVAHSARVWNYWLGGKDNFPADRAAGDAYRGKYPLIETFAKESRDFLRRTVTYLARDAGIRQFLDVGAGLPTANNTHEVAQRIAPESRIVYVDHDPLVLLHVHALLTSTPEGATAYVEADMRDTETVLTGAAKTLDLTQPVALVISDVLGHIVDWDDALSLVRRLVERLPSGSYLSLSHSTASDEAHRAVQDEYNASGAIPYIFREPETTVAFFDGLEMVEPGMVSWPNWRPDANTGTTTARAGWGAVARIP
>NZ_CP010833.1|WP_075264902.1|3356116_3357571_+|helix-turn-helix-domain-containing-protein
MSTTGTTGHEAACPGGARQARETTDRLLRAATRSGAHLIAEAALLVQGWAVLADPIAGAVYSTPAAAAADGVHAAADPHEHPYCLQRPAAGAVLVLAPGPTVPPERAARVATTTAALLDVRGQRAAELRGEQMRLHTTLVRLLLAGHTTAVADTLGGNRLTHATVYRLTGADVPTAHQVLWRAVRPSLAPHADACTLLGRLDGELVVAELHRGGDDGRVLRLVSRVSERHQLLAGMGGPLPLAEMPTAHSDAAAARHSATADRRIVPADAVGTSRLTPLLPAAPYARWAGAVLRPLTAAHQHLLLVWLRTGSKPRAAAALGLSAGTVRARIRELSRLLRADLEDATVQAHLLLALRAPASADPDESEHGDGGGARLEALPAGILDTEAVRAWAHGLVGGLEPHLRIALACWLDHHARTAPAAAELHVHRTTLSNWLAQCAEHLAQNLGDATVRAEVHLALRATRTGPDDPAALPRRGGRTYRRL
>NZ_CP010833.1|WP_107472797.1|3357644_3358565_+|hypothetical-protein
MDGNAGRNLWERVRGGRRREPDKMKLSVGIGYGALAGLYSTLGVALSLLVGGPSPGAAALCVLILATGPTVAALLFGRPAYRRRPLWATGQGLLSVLWQVVWLAPFSVLVGAVLQAGSPLWPALLLWLLNSCYCTFWAFHVNREEPGRHSGAKRHGHPTVRNDRPAPPEPRPSRPPLPRSKQEERAITEFGELLAVHPFSPTLPGVDYVQVADHSLALDAYERAKVASAGEVLDTLAEGKVALARLDARMGLDTVRSRTGCFFDPRHGPGVVDVEWAPRGGTSRTVQVCRADAVRLADKRRRRRAG

Crispr_ID: NZ_CP010833_9

• CRISPR_ID: NZ_CP010833_9
• CRISPR_location: 3636680-3637012
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP010833_9

Consensus_repeat	Method
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	PILER-CR
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	CRISPRCasFinder

spacers of NZ_CP010833_9

>9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder
CGACTCCGTCGCCGCGGCCGCAGCCAGATCGGG
>9.2|3636769|33|NZ_CP010833|PILER-CR,CRISPRCasFinder
GTACCTGGCGGCCGTGGACGCGGTGCGGAAGGC
>9.3|3636830|33|NZ_CP010833|PILER-CR,CRISPRCasFinder
GGTGTTGAGGGTGTCGAGCTTCGACACTTTTTG
>9.4|3636891|33|NZ_CP010833|PILER-CR,CRISPRCasFinder
CAGGGCCTCAAACCCCGGAAGTTGACGAAGAAG
>9.5|3636952|33|NZ_CP010833|CRISPRCasFinder
CTTCTCAAGTAGGGCGGCGAGTTGAGGCATCCC

CRISPR arrays and Neighbor proteins around NZ_CP010833_9

CRISPR arrays

The CRISPR arrays of NZ_CP010833_9

>merge|NZ_CP010833|9|3636680-3637012|PILER-CR,CRISPRCasFinder
GTGGTCCCCGCGTGCGCGGGGGTGTTCCCGACTCCGTCGCCGCGGCCGCAGCCAGATCGGGGTGGTCCCCGCGTGCGCGGGGGTGTTCCGTACCTGGCGGCCGTGGACGCGGTGCGGAAGGCGTGGTCCCCGCGTGCGCGGGGGTGTTCCGGTGTTGAGGGTGTCGAGCTTCGACACTTTTTGGTGGTCCCCGCGTGCTCGGGGGTGTTCCCAGGGCCTCAAACCCCGGAAGTTGACGAAGAAGGTGGTCCCCGCGTGCTCGGGGGTGTTCCCTTCTCAAGTAGGGCGGCGAGTTGAGGCATCCCGTGGTCCCCGCGTGCGCGGGGCCGGTCC

>NZ_CP010833|9|1|3636680-3636951|PILER-CR
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	CGACTCCGTCGCCGCGGCCGCAGCCAGATCGGG
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	GTACCTGGCGGCCGTGGACGCGGTGCGGAAGGC
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	GGTGTTGAGGGTGTCGAGCTTCGACACTTTTTG
GTGGTCCCCGCGTGCTCGGGGGTGTTCC	CAGGGCCTCAAACCCCGGAAGTTGACGAAGAAG
GTGGTCCCCGCGTGCTCGGGGGTGTTCC

>NZ_CP010833|9|9|3636680-3637012|CRISPRCasFinder
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	CGACTCCGTCGCCGCGGCCGCAGCCAGATCGGG
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	GTACCTGGCGGCCGTGGACGCGGTGCGGAAGGC
GTGGTCCCCGCGTGCGCGGGGGTGTTCC	GGTGTTGAGGGTGTCGAGCTTCGACACTTTTTG
GTGGTCCCCGCGTGCTCGGGGGTGTTCC	CAGGGCCTCAAACCCCGGAAGTTGACGAAGAAG
GTGGTCCCCGCGTGCTCGGGGGTGTTCC	CTTCTCAAGTAGGGCGGCGAGTTGAGGCATCCC
GTGGTCCCCGCGTGCGCGGGGCCGGTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075265105.1|3641987_3642647_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|366102
NZ_CP010833.1|WP_075265094.1|3630393_3630576_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265099.1|3633675_3634554_+|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|366166
NZ_CP010833.1|WP_006126349.1|3639822_3640143_-|multidrug-efflux-SMR-transporter	unknown	unknown	gnl|CDD|224987
NZ_CP010833.1|WP_075265092.1|3628907_3629495_-|RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|224511
NZ_CP010833.1|WP_075265096.1|3631549_3632131_+|hypothetical-protein	unknown	unknown	gnl|CDD|380217
NZ_CP010833.1|WP_075265097.1|3632221_3632662_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670
NZ_CP010833.1|WP_075265106.1|3642700_3643360_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_010063236.1|3640294_3640681_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265108.1|3645093_3645474_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265098.1|3633041_3633569_-|CGNR-zinc-finger-domain-containing-protein	unknown	unknown	gnl|CDD|378696
NZ_CP010833.1|WP_075265093.1|3629783_3630326_+|Asp23/Gls24-family-envelope-stress-response-protein	unknown	unknown	gnl|CDD|377129
NZ_CP010833.1|WP_079181482.1|3640894_3641695_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|238045
NZ_CP010833.1|WP_075265107.1|3643537_3644965_+|hypothetical-protein	unknown	unknown	gnl|CDD|214549
NZ_CP010833.1|WP_075265095.1|3630572_3631553_+|hypothetical-protein	unknown	unknown	gnl|CDD|380217
NZ_CP010833.1|WP_075265101.1|3637279_3639127_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|224926
NZ_CP010833.1|WP_075265102.1|3639292_3639754_-|multidrug-efflux-SMR-transporter	unknown	unknown	gnl|CDD|224987
NZ_CP010833.1|WP_075265104.1|3641691_3641928_+|DUF397-domain-containing-protein	unknown	unknown	gnl|CDD|377231
NZ_CP010833.1|WP_075265091.1|3628254_3628911_-|hypothetical-protein	unknown	unknown	gnl|CDD|377129
NZ_CP010833.1|WP_075265100.1|3635402_3636431_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|237030

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075265105.1|3641987_3642647_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	5.76759e-08
NZ_CP010833.1|WP_075265099.1|3633675_3634554_+|alpha/beta-hydrolase	gnl|CDD|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	1.48774e-34
NZ_CP010833.1|WP_006126349.1|3639822_3640143_-|multidrug-efflux-SMR-transporter	gnl|CDD|224987	COG2076, EmrE, Membrane transporters of cations and cationic drugs [Inorganic ion transport and metabolism].	3.1665e-19
NZ_CP010833.1|WP_075265092.1|3628907_3629495_-|RNA-polymerase-sigma-factor	gnl|CDD|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	2.95609e-43
NZ_CP010833.1|WP_075265096.1|3631549_3632131_+|hypothetical-protein	gnl|CDD|380217	NF033218, anchor_AmaP, alkaline shock response membrane anchor protein AmaP. The founding member of this family, AmaP (Asp23 membrane anchoring protein), is related to Asp23 through part of its length, but includes a highly hydrophobic N-terminal region that should make it an integral membrane protein. Asp23 (alkaline shock protein of 23 kDa), described in PMID:7864904, is a cytosolic protein in Staphylococcus aureus, strongly induced by a pH shift from 7 to 10, and also recruited to the membrane. AmaP appears to be the partner protein with an integral membrane segment and the ability to anchor Asp23 to the membrane. This model was built to identify full-length homologs of AmaP, while excluding Asp23. Some but not all members of this family score above the cutoffs of Pfam model version PF03780.11, but full-length homologs of Asp23 score considerably higher. Asp23 family members previously were known as DUF322.	0.00473393
NZ_CP010833.1|WP_075265097.1|3632221_3632662_+|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	1.43113e-14
NZ_CP010833.1|WP_079181482.1|3640894_3641695_+|helix-turn-helix-domain-containing-protein	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	0.00834109
NZ_CP010833.1|WP_075265098.1|3633041_3633569_-|CGNR-zinc-finger-domain-containing-protein	gnl|CDD|378696	pfam11706, zf-CGNR, CGNR zinc finger. This family consists of a C-terminal zinc finger domain. It seems likely to be DNA-binding given the conservation of many positively charged residues. The domain is named after a highly conserved motif found in many members of the family.	1.05903e-15
NZ_CP010833.1|WP_075265093.1|3629783_3630326_+|Asp23/Gls24-family-envelope-stress-response-protein	gnl|CDD|377129	pfam03780, Asp23, Asp23 family, cell envelope-related function. The alkaline shock protein Asp23 was identified as an alkaline shock protein that was expressed in a sigmaB-dependent manner in Staphylococcus aureus. Following an alkaline shock Asp23 accumulates in the soluble protein fraction of the S. aureus cell. Asp23 is one of the most abundant proteins in the cytosolic protein fraction of stationary S. aureus cells, with a copy-number of >25000 per cell. A second Asp23-family protein, AmaP, which is encoded within the asp23-operon, is required to localize Asp23 to the cell membrane. The overall function for the family is thus a cell envelope-related one in Gram-positive bacteria.	9.56194e-34
NZ_CP010833.1|WP_075265107.1|3643537_3644965_+|hypothetical-protein	gnl|CDD|214549	smart00191, Int_alpha, Integrin alpha (beta-propellor repeats). Integrins are cell adhesion molecules that mediate cell-extracellular matrix and cell-cell interactions. They contain both alpha and beta subunits. Alpha integrins are proposed to contain a domain containing a 7-fold repeat that adopts a beta-propellor fold. Some of these domains contain an inserted von Willebrand factor type-A domain. Some repeats contain putative calcium-binding sites. The 7-fold repeat domain is homologous to a similar domain in phosphatidylinositol-glycan-specific phospholipase D.	1.79795e-05
NZ_CP010833.1|WP_075265102.1|3639292_3639754_-|multidrug-efflux-SMR-transporter	gnl|CDD|224987	COG2076, EmrE, Membrane transporters of cations and cationic drugs [Inorganic ion transport and metabolism].	2.89798e-25
NZ_CP010833.1|WP_075265101.1|3637279_3639127_-|MBL-fold-metallo-hydrolase	gnl|CDD|224926	COG2015, COG2015, Alkyl sulfatase and related hydrolases [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP010833.1|WP_075265095.1|3630572_3631553_+|hypothetical-protein	gnl|CDD|380217	NF033218, anchor_AmaP, alkaline shock response membrane anchor protein AmaP. The founding member of this family, AmaP (Asp23 membrane anchoring protein), is related to Asp23 through part of its length, but includes a highly hydrophobic N-terminal region that should make it an integral membrane protein. Asp23 (alkaline shock protein of 23 kDa), described in PMID:7864904, is a cytosolic protein in Staphylococcus aureus, strongly induced by a pH shift from 7 to 10, and also recruited to the membrane. AmaP appears to be the partner protein with an integral membrane segment and the ability to anchor Asp23 to the membrane. This model was built to identify full-length homologs of AmaP, while excluding Asp23. Some but not all members of this family score above the cutoffs of Pfam model version PF03780.11, but full-length homologs of Asp23 score considerably higher. Asp23 family members previously were known as DUF322.	1.42465e-06
NZ_CP010833.1|WP_075265104.1|3641691_3641928_+|DUF397-domain-containing-protein	gnl|CDD|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	1.09605e-17
NZ_CP010833.1|WP_075265091.1|3628254_3628911_-|hypothetical-protein	gnl|CDD|377129	pfam03780, Asp23, Asp23 family, cell envelope-related function. The alkaline shock protein Asp23 was identified as an alkaline shock protein that was expressed in a sigmaB-dependent manner in Staphylococcus aureus. Following an alkaline shock Asp23 accumulates in the soluble protein fraction of the S. aureus cell. Asp23 is one of the most abundant proteins in the cytosolic protein fraction of stationary S. aureus cells, with a copy-number of >25000 per cell. A second Asp23-family protein, AmaP, which is encoded within the asp23-operon, is required to localize Asp23 to the cell membrane. The overall function for the family is thus a cell envelope-related one in Gram-positive bacteria.	0.00222454
NZ_CP010833.1|WP_075265100.1|3635402_3636431_+|MarR-family-transcriptional-regulator	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	5.09711e-11

Protein sequences

>NZ_CP010833.1|WP_075265100.1|3635402_3636431_+|MarR-family-transcriptional-regulator
MVTQHFSSALSAPAVPTAYPMAKPGYGKRSAPDQQPRTRDDFATLPTRERYVAGFVDHLPEGAAMSVKQLAKQLPLYGQQAISTALNALSVAGHLRRVRCAVGAGDETRWAFRTFWSRTARDNEWWNAYLATEKAARTAAPAEPAAASAPPAPAPVAVPQQRTAPEAAPAPAPATAPTAPAAAPTVPPTAPSPAYLALAELGRKDIRLALSADDCAALEAQAAEWLARGVSTDYLTTALTAGLPAQVDCPPRFVRRRLTDKIPPQLPGGPASPGTGTPPPVARILVECTDCGRPGQPEALPDGLCRPCRATHSPGGQLAPDPTEVAAVKAHMANLRDLLKPV
>NZ_CP010833.1|WP_075265099.1|3633675_3634554_+|alpha/beta-hydrolase
MTEVRHRYTSVHEHRVFYREAGPAGAPTVVLLHGFPTSSRMFRHLIPALADRYHVIAPDHLGFGQSDTPPADTFDYTFDSLADVTQALLAQLGVERYAIYVQDYGAPIGWRLALRNPDAVTAIVSQNGNAYDEGFVPEFWAPVWAYAHSQDPSTEEAVRGALSEEAIRWQYTHGVAEPELVDPDTWATDHREISRPGLDRIQLDLFRDYASNPPLYPRLHEYFRSSQVPLLAIWGAEDEIFGPDGARAFAKDLKNAHIQLVPGGGHFLLESHLDTVVDAMRGFLGQNASVRA
>NZ_CP010833.1|WP_075265098.1|3633041_3633569_-|CGNR-zinc-finger-domain-containing-protein
MIGEEALLEALNSTPVRDGVPTDLWQDERELSRWAIRYGGGAPSEQACLRRTRGALQAVVRGESGPDVLTPVLAEVRKVPRLDAGRLEWHLEVEAERRLAVELVLAWARVQEESPGRLRPCANSECRLFLLDRSRANTARWCSMKTCGNRIKARRHHARQRPAGSPEPADTEGRA
>NZ_CP010833.1|WP_075265097.1|3632221_3632662_+|MarR-family-transcriptional-regulator
MTTKQQPRTASDQAMWDSVLGLHTFVERQLAHALQRRFGVGLSEYRALEVLTRAEKGEHRMQELADRIGLGQSSVTRLVGRLENAGYAYKDTCDDDKRGVYAVITDAGRKHYQDARSTYADVLGSALDAASDDDQLARAVQALRGA
>NZ_CP010833.1|WP_075265096.1|3631549_3632131_+|hypothetical-protein
MNSPSAVNRTLTALAGIALLGAGLWLLGATRAVVDHLPARWPAPPADGVLLDRQGLASLRETSWWAPAVMAAGTVLTLLCLAWAVSRTPVRRLRPTGPLSTARTQLRLTALEDAVCEDARRIEGVAQARCRIALSRTSAHLALRVRTLPGYAAKDVLDSLGTVSTTVEHALHPRELNTRTRVSAQRHAAPHVR
>NZ_CP010833.1|WP_075265095.1|3630572_3631553_+|hypothetical-protein
MIPAAARGTTTVSARAVARIAQQAATETPNAVGTVRGTATVRGQRAQVSVRLGLPWPADLGRRAGEVQRHVASRTGELTGLSVRVSRLRVVRLQRPTGAGPAAVFETTASAVEGRVPRRWWSARPTPVVVAALLGAAAAGLLTADMAAVHLFGHAPAAWRTGLIDRLATTSPAAGSVTVAAAAMAVAGLWLLLLACTPGLRKRHVVAGFSARRSIALDRSAVASAVRDRVLDTDGVDSVRVRVGRRRVRVRADLAFGDRAAAREQAGAAARDALADCRLNRPLRVGLRLRTTSTWDPAPPGPEPASAGGTVGTGGTVGEAKLKESP
>NZ_CP010833.1|WP_075265094.1|3630393_3630576_+|hypothetical-protein
MNGRSMGLLVGIALGFAAYFGGFAAFLLVGALGAVGWGAGAWLDREGAAHLRDLFDRDRR
>NZ_CP010833.1|WP_075265093.1|3629783_3630326_+|Asp23/Gls24-family-envelope-stress-response-protein
MVATDTKTTPSTDSVTNSGKAARFEQPAGTGRSAGTSLSAGATGAEAPAGDRGRTSIADVVVVKIAGMAAREIPGVHDMGGGLSRTIGAVRDRVPGGRPNVGRGVKVEVGERQTAIDLELVVEYGVSIKELASEVRENVILAVERITGLEVVEVNIAIDDVRLPDDEDSSASGGDQSRVA
>NZ_CP010833.1|WP_075265092.1|3628907_3629495_-|RNA-polymerase-sigma-factor
MTGNPPPGEPPDVEGGRSDDTLMTERAAEGDEDAFAVLVRRHAPSLLRLATRLLGDRAEAEDAVQEAFVGAWRSLPEFQGRSSFGTWMYRIVTNRCLNILRARRPQAPLNELPDLPAPAHATAPDRITEGRAALHDVQEALSTLSPEQRICWTLRTLDGRSYAFIAKTVGISEQAVRARVFRARRQLTHSLGAWQ
>NZ_CP010833.1|WP_075265091.1|3628254_3628911_-|hypothetical-protein
MNNLPPETRTDPDDETLPCGRLLSQVWADWEDDVHDDHTAQCAHCRLAVADLERLESQVRSLDADPAQQPVDATYFIDRVMDVVRLELRPGQPLPLGEADEDLRIMENVAARALRRAAEEVPGVRAGSCRLGGRPVNVDLSVHVPLTTSDVQALAEEIRDRVDATAREGLGLHLGEINVRITDLVDDDASPRSPRSARSSRSPRSPQSPRSAQEGSAP
>NZ_CP010833.1|WP_075265101.1|3637279_3639127_-|MBL-fold-metallo-hydrolase
MTTAATSPDSTRDSSTPDFADRTDFEDADRGLVAGPANAKITAEDGRVVWDFDATAFLREDCPDTADPSLWRQSQLCARAGLYEVTEGVYQIRGFDLSNMTLIEGERGVVVVDPLVSQECAAEGLALYRAHRGDQPVTAVVFTHSHIDHFGGTLGVIGPDDDVPIVAPAGFMENSVAENVYAGTAMLRRGAYHTGWELDPDPRGLIGVGLGFAASTGMPSLLPPTLEVTRTGQEERLDGVLFRFQLTPGTEAPSELNFHLPERRALCMAENASHNLHNIQTLRGALVRDARIWSRYLTESITLYAADSDVLFASHHWPTWDTERLTAFLSEQRDLYGYLHDQTLRLLNQGYTGIEIAEMIELPPRLARAWHARGYYGSVSHNVKAIYHRYMGWYDGHPASLWEHPPTESAHRYVDCMGGLGAVLAKARSYLDAGDLRFAAQLLKHATFAAPGDSRAKELLAETFERLGYGAECGTWRNNYLVGAQELRNGVQPVPIAADSMSAALSVDQVFDSLAIRVNGPRAWDHDLAVVWRFTDLDTTYRTSLRNGVLVHHPVADGSAADSADLTLTLTKAQLMDLLGGLGFDGIEQTGDPGALTALMSVLDDPDPGFAIVTP
>NZ_CP010833.1|WP_075265102.1|3639292_3639754_-|multidrug-efflux-SMR-transporter
MSNAAQNTAAAATATATKNSSTNAWLSLLLAGVFEIGYALAVGGSEGFTVLTWSLVAVVFFLLTLYALSLALRTIDVSIGYAVWAGIGAVGAAVLGPLFFDETLTVAKGVWLAVIIVGVIWLKLADRTKPAAEAVAPARSTGRLADRADAVRA
>NZ_CP010833.1|WP_006126349.1|3639822_3640143_-|multidrug-efflux-SMR-transporter
MHWLYLAVAVAFEILVAIAAGKAEGFKNRKWTSITLASGAAATFFLSKALLTFDVGVGYALWTSVAGVGITVLGALFFGQRLNLHKAIGIVLVIGGVVGLQLSGSA
>NZ_CP010833.1|WP_010063236.1|3640294_3640681_-|hypothetical-protein
MTADWIPEYGFHLRKAGVQFDAIRVDGDAGRRLADLMEELVGGEPGPVVSESNGRRGVYFLVPPGSTAGRPWPREVTTFNSATGRISYVPVPALGGDTWPLMWRYPPTRAGRFVHTLILFNAAYALLS
>NZ_CP010833.1|WP_079181482.1|3640894_3641695_+|helix-turn-helix-domain-containing-protein
MARMVAEMARTLRVQRGWTQEQEGKEIGYSAAAISAMETCAQPASDAMLVELQRVHGKGTRIFETARQYMRMERLPEQFKDYALLEEAALSLQLFVTNVVHGLFQTEAYARALIGGGHPPLPDARVEELVQLRMARTALFDRDPLPMIEIIIDESVLRRVIGSEEIMREQLLHLVQCARRRNVTLLVLPLNAGKDGEYDGGRGSMSVLETPEHERLVYLEPQDESLLISDPAKVSVYAQRYAKIRSQALGPRESLDLIKRLAGVTE
>NZ_CP010833.1|WP_075265104.1|3641691_3641928_+|DUF397-domain-containing-protein
MSSTLRWFKSSYSSESGGECIEVAFDWRTSSYSSDSGGECVEVAACPHSVHVRDSKVTDGPVFAVAPDAWSAFVTWAE
>NZ_CP010833.1|WP_075265105.1|3641987_3642647_+|TetR/AcrR-family-transcriptional-regulator
MAVQRAGDAEPEPEPESAHPTPPEGLKSRDRILWAASTMLGEGAGSALSVRAVAERAGVSTGSLRHHFPTQRALMEAMLKVIFDLVLPEASFRDTSISPRDRLLGCVQGLLVPPDSARGAREAWLTVHERYIAQEPTQAMRAEYQAMQREVTRRVEECLNVLVEEGALAPGDTTRRARFLLTLANGVAVEQVLPSEDAHLATELDMLRTGVDLVLDNRV
>NZ_CP010833.1|WP_075265106.1|3642700_3643360_-|hypothetical-protein
MGLSWNDRRLERRVKPGDGKPLKPFRWWQMTRRSLLSIALPVGGGLSATYTVEVKHGGDPETGVVRARLYRDGLCEAESKLPARFPVPGGTIEVRRSEVGMRRCHFVADGDGSETRLVPDSRSAEGRRMNFAREHPAASALIGAVSVVLLLIGVGLNLLQAAQPISEIPAIAESLGTFESPLRLPIWLNVTLGLGAAFGATERAMRMRYHWLLDSGAGT
>NZ_CP010833.1|WP_075265107.1|3643537_3644965_+|hypothetical-protein
MAGHTARTRRFAALAATAAMTVAATTLSGGTAGATALPVPHDINGDGYGDIVLPAPGATVAGKPYAGAIVVLYGSAKGVSAAKRAVITQNSPGVPGTAEEGDSFGASIALADLDKDGFADIVVGSPQEKIGSKQSAGAVTVLWGGKKGPVSGVALPTREEKLGQAGQDVAAWSGPDGAQVIVVNRNDSTRLTGPFKRSGKIVASSYHHNETGFMNAAAYGDLNGDKAADRVLVGGRSDDKSGGSVFVNSTWEKINRLHGGDGLFAAVGDVNGDGYGDVVLGDPDDPRPDAPLGHLGGAVHVWFGSKTGVAYDKAPMTIHQDTAGVPGGGERGDAFGASVAVADLNKDGAAEIIVGTPGEAIGKKADAGGVVVIPGRRTGQLGAGSYAFTQDTAGVPGAVEAGDRFGATVSAGDLNKDGRPDLVVGAAQENGQGAVWVLPGGKSGLPLYTSSASYGPGSLGLSKNQWLLLGGDHRQ
>NZ_CP010833.1|WP_075265108.1|3645093_3645474_-|hypothetical-protein
MRLIRGTITRTAMAATVLATGAMLTMGGTAGAAEAAGTIHGCPSGAVCVYPGAGWNGDKPIYRFYSYGVHKIYNQFGTDRIFNNQTGGAKAYACKGANGTNCLGNQAAGTYWDYDITPINSIKLAK

Crispr_ID: NZ_CP010833_10

• CRISPR_ID: NZ_CP010833_10
• CRISPR_location: 3670086-3670169
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_10

Consensus_repeat	Method
AGCCCCTCCGGCGATCGAGGAGC	CRISPRCasFinder

spacers of NZ_CP010833_10

>10.1|3670109|38|NZ_CP010833|CRISPRCasFinder
CCTCGGAGAGCCCGCACGGGACAAGAGCCCGTATTTCA

CRISPR arrays and Neighbor proteins around NZ_CP010833_10

CRISPR arrays

The CRISPR arrays of NZ_CP010833_10

>merge|NZ_CP010833|10|3670086-3670169|CRISPRCasFinder
AGCCCCTCCGGCGATCGAGGAGCCCTCGGAGAGCCCGCACGGGACAAGAGCCCGTATTTCAAGCCCCTCCGGCGATTGAGGAGC

>NZ_CP010833|10|10|3670086-3670169|CRISPRCasFinder
AGCCCCTCCGGCGATCGAGGAGC	CCTCGGAGAGCCCGCACGGGACAAGAGCCCGTATTTCA
AGCCCCTCCGGCGATTGAGGAGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075268407.1|3663797_3664619_-|NAD(P)H-binding-protein	unknown	unknown	gnl|CDD|187578
NZ_CP010833.1|WP_075265120.1|3660035_3660377_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265128.1|3672661_3673201_-|orotate-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234771
NZ_CP010833.1|WP_075265134.1|3678045_3679209_+|pyridoxal-phosphate-dependent-aminotransferase	unknown	unknown	gnl|CDD|236095
NZ_CP010833.1|WP_075265123.1|3664750_3665668_-|alpha/beta-hydrolase	unknown	unknown	gnl|CDD|223730
NZ_CP010833.1|WP_006126322.1|3668054_3668468_-|DUF3151-domain-containing-protein	unknown	unknown	gnl|CDD|378646
NZ_CP010833.1|WP_075265122.1|3662323_3663661_-|two-component-sensor-histidine-kinase	unknown	unknown	gnl|CDD|226951
NZ_CP010833.1|WP_075265125.1|3668555_3670064_-|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075265129.1|3673258_3674065_-|aldose-epimerase	unknown	unknown	gnl|CDD|185698
NZ_CP010833.1|WP_075265130.1|3674085_3674982_-|carbon-monoxide-dehydrogenase	unknown	unknown	gnl|CDD|176865
NZ_CP010833.1|WP_006126329.1|3661658_3662327_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP010833.1|WP_075265127.1|3671484_3672516_-|class-II-fructose-bisphosphate-aldolase	unknown	unknown	gnl|CDD|236406
NZ_CP010833.1|WP_075265133.1|3677603_3677906_-|hypothetical-protein	unknown	unknown	gnl|CDD|226728
NZ_CP010833.1|WP_030722149.1|3667075_3667924_-|tryptophan-2,3-dioxygenase	unknown	unknown	gnl|CDD|188272
NZ_CP010833.1|WP_075265131.1|3675094_3676693_-|polyamine-aminopropyltransferase	unknown	unknown	gnl|CDD|235139
NZ_CP010833.1|WP_075265124.1|3665856_3667083_-|kynureninase	unknown	unknown	gnl|CDD|226363
NZ_CP010833.1|WP_075265126.1|3670204_3671386_-|pyridoxal-phosphate-dependent-aminotransferase	unknown	unknown	gnl|CDD|224090
NZ_CP010833.1|WP_075265121.1|3660387_3661593_-|cytochrome-P450	unknown	unknown	gnl|CDD|225035
NZ_CP010833.1|WP_159027426.1|3679305_3679533_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265132.1|3676760_3677282_-|DUF2617-family-protein	unknown	unknown	gnl|CDD|378512

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075268407.1|3663797_3664619_-|NAD(P)H-binding-protein	gnl|CDD|187578	cd05269, TMR_SDR_a, triphenylmethane reductase (TMR)-like proteins, NMRa-like, atypical (a) SDRs. TMR is an atypical NADP-binding protein of the SDR family. It lacks the active site residues of the SDRs but has a glycine rich NAD(P)-binding motif that matches the extended SDRs. Proteins in this subgroup however, are more similar in length to the classical SDRs. TMR was identified as a reducer of triphenylmethane dyes, important environmental pollutants. This subgroup also includes Escherichia coli NADPH-dependent quinine oxidoreductase (QOR2), which catalyzes two-electron reduction of quinone; but is unlikely to play a major role in protecting against quinone cytotoxicity. Atypical SDRs are distinct from classical SDRs. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.41348e-55
NZ_CP010833.1|WP_075265128.1|3672661_3673201_-|orotate-phosphoribosyltransferase	gnl|CDD|234771	PRK00455, pyrE, orotate phosphoribosyltransferase; Validated.	1.55706e-60
NZ_CP010833.1|WP_075265134.1|3678045_3679209_+|pyridoxal-phosphate-dependent-aminotransferase	gnl|CDD|236095	PRK07777, PRK07777, putative succinyldiaminopimelate transaminase DapC.	0
NZ_CP010833.1|WP_075265123.1|3664750_3665668_-|alpha/beta-hydrolase	gnl|CDD|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	4.4934e-15
NZ_CP010833.1|WP_006126322.1|3668054_3668468_-|DUF3151-domain-containing-protein	gnl|CDD|378646	pfam11349, DUF3151, Protein of unknown function (DUF3151). This family of proteins with unknown function appears to be restricted to Actinobacteria.	3.75583e-74
NZ_CP010833.1|WP_075265122.1|3662323_3663661_-|two-component-sensor-histidine-kinase	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.99946e-34
NZ_CP010833.1|WP_075265125.1|3668555_3670064_-|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.52624e-75
NZ_CP010833.1|WP_075265129.1|3673258_3674065_-|aldose-epimerase	gnl|CDD|185698	cd09021, Aldose_epim_Ec_YphB, aldose 1-epimerase, similar to Escherichia coli YphB. Proteins similar to Escherichia coli YphB are uncharacterized members of the aldose-1-epimerase superfamily. Aldose 1-epimerases or mutarotases are key enzymes of carbohydrate metabolism, catalyzing the interconversion of the alpha- and beta-anomers of hexose sugars such as glucose and galactose. This interconversion is an important step that allows anomer specific metabolic conversion of sugars. Studies of the catalytic mechanism of the best known member of the family, galactose mutarotase, have shown a glutamate and a histidine residue to be critical for catalysis; the glutamate serves as the active site base to initiate the reaction by removing the proton from the C-1 hydroxyl group of the sugar substrate, and the histidine as the active site acid to protonate the C-5 ring oxygen.	1.32638e-55
NZ_CP010833.1|WP_075265130.1|3674085_3674982_-|carbon-monoxide-dehydrogenase	gnl|CDD|176865	cd07823, SRPBCC_5, Ligand-binding SRPBCC domain of an uncharacterized subfamily of proteins. Uncharacterized group of the SRPBCC (START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC) domain superfamily. SRPBCC domains have a deep hydrophobic ligand-binding pocket and they bind diverse ligands. SRPBCC domains include the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domains of mammalian STARD1-STARD15, the C-terminal catalytic domains of the alpha oxygenase subunit of Rieske-type non-heme iron aromatic ring-hydroxylating oxygenases (RHOs_alpha_C), Class I and II phosphatidylinositol transfer proteins (PITPs), Bet v 1 (the major pollen allergen of white birch, Betula verrucosa), CoxG, CalC, and related proteins. Other members of the superfamily include PYR/PYL/RCAR plant proteins, the aromatase/cyclase (ARO/CYC) domains of proteins such as Streptomyces glaucescens tetracenomycin, and the SRPBCC domains of Streptococcus mutans Smu.440 and related proteins.	4.33846e-20
NZ_CP010833.1|WP_075265127.1|3671484_3672516_-|class-II-fructose-bisphosphate-aldolase	gnl|CDD|236406	PRK09197, PRK09197, fructose-bisphosphate aldolase; Provisional.	0
NZ_CP010833.1|WP_075265133.1|3677603_3677906_-|hypothetical-protein	gnl|CDD|226728	COG4278, COG4278, Uncharacterized conserved protein [Function unknown].	5.17621e-08
NZ_CP010833.1|WP_030722149.1|3667075_3667924_-|tryptophan-2,3-dioxygenase	gnl|CDD|188272	TIGR03036, trp_2_3_diox, tryptophan 2,3-dioxygenase. Members of this family are tryptophan 2,3-dioxygenase, as confirmed by several experimental characterizations, and by conserved operon structure for many of the other members. This enzyme represents the first of a two-step degradation to L-kynurenine, and a three-step pathway (via kynurenine) to anthranilate plus alanine. [Energy metabolism, Amino acids and amines].	5.45809e-145
NZ_CP010833.1|WP_075265131.1|3675094_3676693_-|polyamine-aminopropyltransferase	gnl|CDD|235139	PRK03612, PRK03612, polyamine aminopropyltransferase.	0
NZ_CP010833.1|WP_075265124.1|3665856_3667083_-|kynureninase	gnl|CDD|226363	COG3844, COG3844, Kynureninase [Amino acid transport and metabolism].	7.19905e-142
NZ_CP010833.1|WP_075265126.1|3670204_3671386_-|pyridoxal-phosphate-dependent-aminotransferase	gnl|CDD|224090	COG1168, MalY, Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities [Amino acid transport and metabolism].	6.38446e-145
NZ_CP010833.1|WP_075265121.1|3660387_3661593_-|cytochrome-P450	gnl|CDD|225035	COG2124, CypX, Cytochrome P450 [Secondary metabolites biosynthesis, transport, and catabolism].	1.06071e-97
NZ_CP010833.1|WP_006126329.1|3661658_3662327_-|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	9.31051e-75
NZ_CP010833.1|WP_075265132.1|3676760_3677282_-|DUF2617-family-protein	gnl|CDD|378512	pfam10936, DUF2617, Protein of unknown function DUF2617. This bacterial family of proteins has no known function.	1.29172e-66

Protein sequences

>NZ_CP010833.1|WP_075265125.1|3668555_3670064_-|DHA2-family-efflux-MFS-transporter-permease-subunit
MAAAGSAPGEIRVASPVGRWVVLTTVLGSGMAMLDSTVINVALPRIGEDLGTDMAALQWTVNAYMLTLAGLILLGGALGDRYGRRRVFVVGVVWFAVASLLCGIAPNAGVLIAARALQGVGGALLTPGSLALIQASFHPDDRARAVGLWSGFGGVGAAVGPFVGGWLVDGPGWRWVFLLNLPLAAICVPVALRHVPESRDPAAHGRFDVLGAALGALALAGVTYALIEAPEQGASPLVIGSAVGGLLLGAAFVRVERRRADPMLPPSIFRSRLFTSVNLVTFCVYAALGGFFFLSAIQLQVVAGYSALGAGTALLPTTVLMLLFSAQAGELGRRIGPRIPLTAGPLLAAAGMLLMLRVGPDSASFGGYVTEVLPAVLVLGAGLVVVVAPLTATVLAAVDTGRAGLASGINNAAARAAGLIAVAALPLLAGMGPEAYRDAGEFATTFRRAMPMCAGLLVAGAFLAWWTVRTPAATAAVRSERPECAVHCGVTAPPLEPQRREG
>NZ_CP010833.1|WP_006126322.1|3668054_3668468_-|DUF3151-domain-containing-protein
MSIHENLLGGPAPTHLPDDPEPRELLAAGTPPAEVAAKYPTSSLAWAQLADEAYEGGRVVESYAYARTGYHRGLDSLRRAGWKGHGPVPFEHEPNRGFLRALHALARAAGSIGETEEHERCTTFLRDSSPTAADILG
>NZ_CP010833.1|WP_030722149.1|3667075_3667924_-|tryptophan-2,3-dioxygenase
MSTNHPDPEATGADTPYLDFAGTTPYEDYVQADVLTHLQHLRSDDPGEMVFLVTTQVMELWFTVIVHEWETATRALREDRIPVARDALKRSLRELEALNESWRPLAGLTPAQFNSYRGSLGEGSGFQSAMYRRMEFLLGDKSASMLVPHRGAPRVYAELEKALGEPSLYDETLALLARRGYAIPEAVTTRDLTKRYEPSPEVEAVWAEIYASDDQNDELVRLGELLTDVGELVWRWRNDHLVATRRAMGSKTGTGGSAGVAWLEKRATKNVFPELWTARSHV
>NZ_CP010833.1|WP_075265124.1|3665856_3667083_-|kynureninase
MSETTTATTTEALRERALKLDAADPLADRRELFALDDGVYLDGNSLGALPAHVPARVQDVLTRQWGELRIRSWDESGWWTAPERIGDRIAPLVGAAAGQIVVGDSTSVNVFKAVVAAARIAGEGRDEILVDATTFPTDGYIAASAARLTGHRLVPVAPADVPAALGPRTAVVLLNHVDYRSGRLHDLPGLTAAVHAAGAVAVWDLCHSAGALPVGLDEHGVDLAVGCTYKYLNGGPGSPAYLYVAERHQAAFDSPLPGWNSHADPFGMTPGYAPADGSVRGRVGTPDIVSMLTLEAALDVWDGVAVDTVRAKSLALTDFFLECVEAYVPAGRVTSVTPAAHAERGSQVALRCDDAEPVMRRLIERGVVGDLRRPDVLRFGFTPLYVGFADAERAARVLAEVLAGERAA
>NZ_CP010833.1|WP_075265123.1|3664750_3665668_-|alpha/beta-hydrolase
MSDSPGSPDAAARARDEAESASAFAHPPVAPDATAAYGDHPDQVVDFHAPRDGRTAAPLVVLLHGGAWRAPYDRAHVSPLADFLARRGFAVANVEYRRGGDDIPQQRGGEESTAGAGPVAGRWPETFDDVAAALDAMPVLAARALPGADVRRIVVTGHSAGGHLALWAAARHVLPEGSPWRLPAPPPLRGVVALAPIADFAAAVGLGVCGGAVTQLLGGEAGFADRAAHADPGVLLPTGIATAIVQGVEDIVVPEAVSEAYVDAAAKAGETVGLTLLGGVGHFPLIDPAADACAVVAEEITQLAW
>NZ_CP010833.1|WP_075268407.1|3663797_3664619_-|NAD(P)H-binding-protein
MTVLVTGATGTVGRRVVEQLLERGEQVRALTRDPERAEFPAGVEVVGGDLTDPASLAPALHGVTGLHLITFGGEYFAPLETGDEILALAEEAGVRRVTVLHGGGDTPVETAVRASGFAWTVVMPVEFMANALEWAPGIRSEGVVREPFVDRLSAMVHESDIGAVAAVALTEDGHGGQAYLVTGPQVLTVRDRTAAVGEARGADVELVELTEEQALENWRGQGMAEDVIAFLIDVYRDTPLEGRTVSGTVEKVTGRPARTFAQWAQEHAEHFRA
>NZ_CP010833.1|WP_075265122.1|3662323_3663661_-|two-component-sensor-histidine-kinase
MTETQTKTSSPESRAAAGAIDALRDDLLRNVFAYRPLPPLSPDGRLIRRLPEGLRKGVVWTPHALVLFAAFIVMMIGFAEWDYRFLMGVVPAIPVAMTLIRPVAAFWASMLATVFCGILSSQLWGPSAFVAQVVVLVVVAARTRPRAAAWMWLLTLFFGMLLEGGDPSITAPLVTLSALALLVVAVVQIRRDAEREVTVQRTVTAVERDRRTLLEERTTIARELHDVVAHHMSVVAIQAEAAPYRVENPPPELEQAFVTIRENAVAALTELRRVLGVVRAEDYEAPDAPQPTLAALDGLLDNVRETGLETEKVITGAVRELPQGVELSAYRIVQEALSNSLRHAPGASARVELSYVLGGLGLRVVNGPPQGLVKPSPGAGHGITGMRERVAMLNGEMTAGTTADGGYEVAVFLPVPLSEQPERAESGDTAEGNADTVVIDRDGRA
>NZ_CP010833.1|WP_006126329.1|3661658_3662327_-|response-regulator-transcription-factor
MSDTDIRVLIVDDQMMVREGFSVLLNAMPGITVVGEALDGRQALDQVAALRPDVVLMDIRMPEMNGIEATREIVARDADAKVLVLTTFDLDEYVYQALRAGASGFLLKDASARQLADGVRVVASGEALLAPTVTRRLITEFSKLAETPRPPALARIGDLTERETEVLVLIAQGLSNAEIASHLIVAESTIKTHVSRILVKLGLRDRTQAAVFAYEARLVTPG
>NZ_CP010833.1|WP_075265121.1|3660387_3661593_-|cytochrome-P450
MHVSFDPWSPAFVADPYPAYTALRAAGRAHWFEPTGQWLIPHHSDVSALLRDRRLGRTYLHRFSHEEFGRTPPPPEHEPFTTLNGQGILDLEAPDHPRIRRLISKAFTPRTVENLAPTVRRLAAELVEAFVAKGGGDLLAEVAEPLPVAVIAEMLGVPEADRGLLRPWSAAICGMFELNPSEETAAAAVSASVDFSAYLRGLISERRANPGDDLISALIAAHDEGERLTEQEMISTCVLLLNAGHEATVNTTVNGWRTLFHHPEQLAALRADPALLPTAIEELLRYDTPLQMFERWVLDDIEIDGQVIGRGAEVALLFGSANRDPERFARPDVLDLSRTDNPHITFGAGIHFCLGAPLARLELAASFGELLRKAPALRMTAEPEWQPGYVIRGLKELRAEV
>NZ_CP010833.1|WP_075265120.1|3660035_3660377_+|hypothetical-protein
METQTPRREAAVGTAGCLTAFVGALAGLALWAPYGKDGLLDGFEGATNWDVVRYGLPLMVIGGVAAALAVFAALRGRWLWALGLVAAVAGLVAVGHAVDALAGPPRPECSDPC
>NZ_CP010833.1|WP_075265126.1|3670204_3671386_-|pyridoxal-phosphate-dependent-aminotransferase
MGAPYDFDTVVDRRGTWCVQWDGVADRFGVDGLLPFTISDMDFATAPEVLAALRARLDHGVLGYTTWWQDDFRSAIAHWYATRYGTEIDTGQLVYGPSVLSQLSQLLQMWTGEGDGVVVHTPVYDGFRKAITGLGRELRGVPVGDEEALERELARPDAKVLVLCSPHNPTGRVWTADELARTAALAERYGVAVISDEIHADFVHEDGAGRVHVPWTRVAGEGRWALITSGSKAFNFPALTGSYGFIGDPADRTEFLRRMETAEGLASPAVLSLTAHIAAYREGAAWLDAVRSYVAGNLAYVAERLGAAFPELGWVPPQAGYLAWIDLRPLGVEESALQRVLVERERVAIMGGSVYGAPGFVRLNAGCPREKVVRGVEALVRAVESLKTSPSGD
>NZ_CP010833.1|WP_075265127.1|3671484_3672516_-|class-II-fructose-bisphosphate-aldolase
MPIATPEAYAEMLDRAKAGKFAYPAINVTSSQTLHAALRGFAEAESDGIVQISTGGAEFLGGQHNKDMVTGAVALAEFAHIVAAKYDVTIALHTDHCPKDKLDGYVRPLLDVSAERVAKGLNPLFQSHMWDGSAETLADNLAIGQELLAKAAAAKIILEVEITPTGGEEDGVTHEINDELYTTVDDALRTAEALGLGEKGRYLLAASFGNVHGVYKPGNVVLRPELLKDLQAGVSEKYGKPVGSQPFDFVFHGGSGSTAEEIATALENGVVKMNLDTDTQYAFTRPVADHMFRNYDGVLKVDGEVGNKKTYDPRTWGKLAEAGMAARVTEACANLRSTGTKLK
>NZ_CP010833.1|WP_075265128.1|3672661_3673201_-|orotate-phosphoribosyltransferase
MTDVRADLLQQIKDKAVVHGKVTLSSGLEADWYIDLRRVTLDGKAAPLVGQVMLDATAELDYDCVGGLTLGADPVATSMLHASAARGKSLDAFVVRKAQKAHGMQRRIEGTDVKGRRCLVVEDTSTTGGSPLTAVEAVREAGGEVVAVAVIVERGAAPAIAEAGLPYVHVYSVADLDLS
>NZ_CP010833.1|WP_075265129.1|3673258_3674065_-|aldose-epimerase
MSRSEENVRLTVGAAELTVDPVHGCRISSLRIGSTELLRQGDRYGCFPMVPWCGRTGYGQFRNGDELHELPLNSPPHAIHGTGRDTSWNPAYTAADLAEGRAAFYYDLAKPWPYEGRVTQTFELTEDTLTLGLAVETYGDSFPAQAGWHPWFLRTLDGRDAELSFDAAWQEERGGDHLPTGRRIDPQPGPWDDCFGMPDGVDVKLTWPERLELTVKSRSEWVVVYDEQDEAVCVEPQSGPPNGLNTVPRLVTPIDPLEMTTTWSWTRL
>NZ_CP010833.1|WP_075265130.1|3674085_3674982_-|carbon-monoxide-dehydrogenase
MEHEVFVPVPVPTLLRTLGDPARVARCIPGLQQDADASASPLAGRLKLRAGGHTITYRGELLLTGPERDRFSVSGKGVEARGTGAVELALTIGLTATDGGTTIAYSGTADGDGRLVELEEGAALAAAHRLLDRFTQQLVTESLAVREVEDGDGGGGGADADTAADADDAVAAEGLEGDEDDADADAVGEDDVDSGAGGDDDPGSVFDSPVPPPSLDPVAGVEFTVPDEPPAEAAHARRTMIGRSAEEVDHAPPRGRYAPVPSPEAGGASTALRWVAPAAALALASAVVLGRALRRRRP
>NZ_CP010833.1|WP_075265131.1|3675094_3676693_-|polyamine-aminopropyltransferase
MIDQQMPLRGGAARLPVRPRTGRFLVLAAVFVCAACGLVYELELVALASYLIGDSVTQASVVLSVMVFAMGIGSLLAKRLRCRAAVGFGMIEAALALIGGSSALVLYASFAWLGDSQYALVGFSLAIGVLIGAEIPLLMTLIQRVDRQDAGGAVADLFAADYVGALVGGLAFPFLLLPMLGQLTGALFTGAVNAAAGGALVLWVFRRDLSPRSRWLLVLANVSVIAVLATATALVDDFERAARRAVYGDQVRVAVQTGVQEVVVTGTGRDSLGLYLDGRLRVSARDEYRYHEALVHPAMNGPRARVLILGGGDGLAAREVLRYGDVRTVTVVELDPAVTRLARTDPALSELNGHALRDPRLTVVGADAFPWLRADHGRYDVVVSDLPDPGITASTKLYSAEFYGLIAEALAPDGRLVVHAGPLGARAQTFWTVEASVRAGGLATRPYRVTGRYAGLAASPDRGGGGRRDREDWGFLLAAAGRAPQAALAAGGPEPRSLRGRELREGARAAAEARLPGLLPSTLIHPRYWEDA
>NZ_CP010833.1|WP_075265132.1|3676760_3677282_-|DUF2617-family-protein
MLTTLQTAYSDTRAADLAWMLGREPLPALAVLDLRFDGAELQLRLLGASHQVLLHEEHGVCSETVACMPGSSTPLPLGVSKRLGDREYEFAARVESLTQGQFAGRAQELLALVSDHPHGLVGTFPGSPYAFTAMLAQRTEGQVRWRTWHAYPQEGQLVVTRTRVGARIPAAAA
>NZ_CP010833.1|WP_075265133.1|3677603_3677906_-|hypothetical-protein
MDVFIAIVIAAVVVGGLLVVLRATGGSKPAHSRTRGRRSSAASAGGESLTGGDSGGGWWSSWGDSGSGGDSGSGGHSGGHSCGGGSSCGGGGGGCGGGSS
>NZ_CP010833.1|WP_075265134.1|3678045_3679209_+|pyridoxal-phosphate-dependent-aminotransferase
MTQGRPLLNRRLATFGTTIFAEMSALAGRTGSINLGQGFPDTDGPEEIREAAVRALRTGHGNQYPPGPGVPELRNAVAAHQERFYGLTWSPETEVLVTTGATEAIAASLLALLEPDDEVIAFEPYYDSYAACIAMAGAKRVPLTLRAPDFRPDLDELRTLITPRTRLLLLNTPHNPTGTVLTPDELSGIAALAVEHDLLVVTDEVYEHLVFTGGHHPIAALPGMRERTVSISSSGKTFSYTGWKIGWVTGDAPLVAAVRAAKQYLTFVSGGPFQYAIAEALALPDTFFTGFREDMRRKRDLLAEGLRTAGFRVYEPEGTYFITTDISPFGDEDAYAFCRALPERCGVAAVPNSVFYDDPEAGRSQVRFTFCKREEVLRRAVERLCDM
>NZ_CP010833.1|WP_159027426.1|3679305_3679533_-|hypothetical-protein
MKQLRISRRASAAGFSPVPAAGVQFPGDAAPLMESFVRNAFRQRPMACFPVDVDAQDEGARKQLDEMYFPYEQEE

Crispr_ID: NZ_CP010833_11

• CRISPR_ID: NZ_CP010833_11
• CRISPR_location: 3782744-3782889
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP010833_11

Consensus_repeat	Method
GTGGTCCCCGCGCACGCGGGGGTG	CRISPRCasFinder

spacers of NZ_CP010833_11

>11.1|3782768|37|NZ_CP010833|CRISPRCasFinder
TTCCGGCGTTGGACATCCGGACCCACTCCTCCGCAAT
>11.2|3782829|37|NZ_CP010833|CRISPRCasFinder
TTCCCGAGACCGGGCTCGCCTGGCTCCCGTTCATCGC

CRISPR arrays and Neighbor proteins around NZ_CP010833_11

CRISPR arrays

The CRISPR arrays of NZ_CP010833_11

>merge|NZ_CP010833|11|3782744-3782889|CRISPRCasFinder
GTGGTCCCCGCGCACGCGGGGGTGTTCCGGCGTTGGACATCCGGACCCACTCCTCCGCAATGTGGTCCCCGCGCACGCGGGGGTGTTCCCGAGACCGGGCTCGCCTGGCTCCCGTTCATCGCGTGGTCCCCGCGCACGCGGGGGCG

>NZ_CP010833|11|11|3782744-3782889|CRISPRCasFinder
GTGGTCCCCGCGCACGCGGGGGTG	TTCCGGCGTTGGACATCCGGACCCACTCCTCCGCAAT
GTGGTCCCCGCGCACGCGGGGGTG	TTCCCGAGACCGGGCTCGCCTGGCTCCCGTTCATCGC
GTGGTCCCCGCGCACGCGGGGGCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_003967677.1|3772746_3773043_+|type-II-toxin-antitoxin-system-VapB-family-antitoxin	unknown	unknown	gnl|CDD|227737
NZ_CP010833.1|WP_010063062.1|3773920_3774556_-|uracil-phosphoribosyltransferase	unknown	unknown	gnl|CDD|234653
NZ_CP010833.1|WP_069737694.1|3788364_3788877_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224759
NZ_CP010833.1|WP_075268418.1|3774658_3774910_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265210.1|3784923_3785811_+|RNA-polymerase-sigma-factor-SigF	unknown	unknown	gnl|CDD|274373
NZ_CP010833.1|WP_075265201.1|3773226_3773829_+|LytR-C-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|379163
NZ_CP010833.1|WP_010063059.1|3775203_3775755_+|hypothetical-protein	unknown	unknown	gnl|CDD|274869
NZ_CP010833.1|WP_075265211.1|3787002_3787848_+|hypothetical-protein	unknown	unknown	gnl|CDD|236090
NZ_CP010833.1|WP_075265202.1|3777271_3778375_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|275041
NZ_CP010833.1|WP_107472872.1|3783506_3783806_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|316153
NZ_CP010833.1|WP_010063058.1|3775909_3776338_+|nucleoside-deaminase	unknown	unknown	gnl|CDD|223663
NZ_CP010833.1|WP_075265205.1|3780155_3780899_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265207.1|3782997_3783489_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_032776631.1|3791741_3792560_+|hypothetical-protein	unknown	unknown	gnl|CDD|377274
NZ_CP010833.1|WP_075265204.1|3779316_3780159_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|238045
NZ_CP010833.1|WP_075265213.1|3788908_3791440_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075265212.1|3787867_3788083_-|hypothetical-protein	unknown	unknown	gnl|CDD|184256
NZ_CP010833.1|WP_075265209.1|3784421_3784715_+|Dabb-family-protein	unknown	unknown	gnl|CDD|369566
NZ_CP010833.1|WP_030579030.1|3786045_3786912_+|RNA-polymerase-sigma-factor-SigF	unknown	unknown	gnl|CDD|274373
NZ_CP010833.1|WP_075265206.1|3781519_3782476_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|237030

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_003967677.1|3772746_3773043_+|type-II-toxin-antitoxin-system-VapB-family-antitoxin	gnl|CDD|227737	COG5450, COG5450, Transcription regulator of the Arc/MetJ class [Transcription].	9.4912e-09
NZ_CP010833.1|WP_075265201.1|3773226_3773829_+|LytR-C-terminal-domain-containing-protein	gnl|CDD|379163	pfam13399, LytR_C, LytR cell envelope-related transcriptional attenuator. This family appears at the C-terminus of members of the LytR_cpsA_psr, pfam03816, family.	1.33626e-12
NZ_CP010833.1|WP_069737694.1|3788364_3788877_+|MarR-family-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	1.21146e-14
NZ_CP010833.1|WP_075265210.1|3784923_3785811_+|RNA-polymerase-sigma-factor-SigF	gnl|CDD|274373	TIGR02980, SigBFG, RNA polymerase sigma-70 factor, sigma-B/F/G subfamily. This group of similar sigma-70 factors includes clades found in Bacilli (including the sporulation factors SigF:TIGR02885 and SigG:TIGR02850 as well as SigB:TIGR02941), and the high GC gram positive bacteria (Actinobacteria) where a variable number of them are found depending on the lineage.	3.29054e-116
NZ_CP010833.1|WP_010063059.1|3775203_3775755_+|hypothetical-protein	gnl|CDD|274869	TIGR03941, conserved_hypothetical_protein, putative tRNA adenosine deaminase-associated protein. This model describes a protein family about 200 amino acids in length with only five invariant residues, including an Arg, a Ser-Asp pair, and two Gly residues. Members always are found exclusively in Actinobacteria, and always adjacent to homologs of TadA, a tRNA-specific adenosine deaminase from Escherichia coli. Homology, phyletic pattern, and gene neighborhood together suggest a housekeeping function in tRNA metabolism. [Unknown function, General].	2.01291e-14
NZ_CP010833.1|WP_075265211.1|3787002_3787848_+|hypothetical-protein	gnl|CDD|236090	PRK07764, PRK07764, DNA polymerase III subunits gamma and tau; Validated.	2.53511e-09
NZ_CP010833.1|WP_075265202.1|3777271_3778375_-|methyltransferase-domain-containing-protein	gnl|CDD|275041	TIGR04188, conserved_hypothetical_protein, methyltransferase, ATP-grasp peptide maturase system. Members of this protein family are predicted SAM-dependent methyltransferases that regularly occur in the context of a putative peptide modification ATP-grasp enzyme (TIGR04187, related to enzymes of microviridin maturation) and a putative ribosomal peptide modification target (TIGR04186).	6.75015e-95
NZ_CP010833.1|WP_107472872.1|3783506_3783806_+|helix-turn-helix-domain-containing-protein	gnl|CDD|316153	pfam13601, HTH_34, Winged helix DNA-binding domain.	2.85366e-17
NZ_CP010833.1|WP_010063058.1|3775909_3776338_+|nucleoside-deaminase	gnl|CDD|223663	COG0590, CumB, Cytosine/adenosine deaminases [Nucleotide transport and metabolism / Translation, ribosomal structure and biogenesis].	9.82852e-66
NZ_CP010833.1|WP_010063062.1|3773920_3774556_-|uracil-phosphoribosyltransferase	gnl|CDD|234653	PRK00129, upp, uracil phosphoribosyltransferase; Reviewed.	3.53565e-120
NZ_CP010833.1|WP_032776631.1|3791741_3792560_+|hypothetical-protein	gnl|CDD|377274	pfam04264, YceI, YceI-like domain. E. coli YceI is a base-induced periplasmic protein. The recent structure of a member of this family shows that it binds to poly-isoprenoid. The structure consists of an extended, eight-stranded, antiparallel beta-barrel that resembles the lipocalin fold.	2.07884e-54
NZ_CP010833.1|WP_075265204.1|3779316_3780159_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	2.31367e-07
NZ_CP010833.1|WP_075265213.1|3788908_3791440_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	3.76531e-64
NZ_CP010833.1|WP_075265212.1|3787867_3788083_-|hypothetical-protein	gnl|CDD|184256	PRK13700, PRK13700, conjugal transfer protein TraD; Provisional.	0.00211098
NZ_CP010833.1|WP_075265209.1|3784421_3784715_+|Dabb-family-protein	gnl|CDD|369566	pfam07876, Dabb, Stress responsive A/B Barrel Domain. The function of this family is unknown, but it is upregulated in response to salt stress in Populus balsamifera. It is also found at the C-terminus of an fructose 1,6-bisphosphate aldolase from Hydrogenophilus thermoluteolus. Arthrobacter nicotinovorans ORF106 is found in the pA01 plasmid, which encodes genes for molybdopterin uptake and degradation of plant alkaloid nicotine. The structure of one has been solved and the domain forms an a/b barrel dimer. Although there is a clear duplication within the domain it is not obviously detectable in the sequence.	8.94513e-19
NZ_CP010833.1|WP_030579030.1|3786045_3786912_+|RNA-polymerase-sigma-factor-SigF	gnl|CDD|274373	TIGR02980, SigBFG, RNA polymerase sigma-70 factor, sigma-B/F/G subfamily. This group of similar sigma-70 factors includes clades found in Bacilli (including the sporulation factors SigF:TIGR02885 and SigG:TIGR02850 as well as SigB:TIGR02941), and the high GC gram positive bacteria (Actinobacteria) where a variable number of them are found depending on the lineage.	1.77418e-123
NZ_CP010833.1|WP_075265206.1|3781519_3782476_+|MarR-family-transcriptional-regulator	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	1.46447e-05

Protein sequences

>NZ_CP010833.1|WP_075265206.1|3781519_3782476_+|MarR-family-transcriptional-regulator
MAKPGYGKRSAPDQQPRTRHDFALLPTRERYVAGFVDHLPDGASMSVKQLAKQLPLYGQQAISTALKALSVAGHLRRVRCSVGAGDETRWVFRTFWSRTAHDNEWWSIYLATETASQAAAPTPEAPAPPPARPESPAVAGQAPEPTAVPPQRTPPQAPDADPTQTTAPSPSYLALARLGRNDHRLGLSADDCTALEPLAAQWLDRGVTTDYLTNALTAGLPAQIDSPVGLLRRRLIDKLPPRLPAIPSTAADTPTPTRRLLVECTDCGRPGQPEALPDGLCRPCHTAHSAGGQPSPDPTQIAAVKAHMANLRTLLKPV
>NZ_CP010833.1|WP_075265205.1|3780155_3780899_-|hypothetical-protein
MTRLRFLGTTSDDGDCPTLYEIEGTTDILVQGDRVTDPEQLAQLRDVKARETFVLVPRDLLLRFAPRTMATEMVPFTAIASLFREFRHTAFRLETRRGYASDRNSPKWARWKSGADIATEPDNAWRENVRAQTAEGKRFERVRLVDQPLTEGQEFLLDSGLGNVAAGEDIRNLPRTQADRLGLPDHDFWLFDSRLVARFVFDEDDTTLGVVVSEDPAEVALACQARDVAWHHATRTADFAKAVASTG
>NZ_CP010833.1|WP_075265204.1|3779316_3780159_-|helix-turn-helix-transcriptional-regulator
MSTDFQTARVALGARLRELRSEAGLNGKGVAEVLGWQRSKVSRLETGKQTPTASDLAQWSQAVGRPDVATELRGRLVGLESQYRSWRRQLAGGHRARQELAVSETTTTQLIRGVEVSRIPGLFQTADYARHTFEANAEFRRIPRDIEAAVRARMRRQEALYEAGKLFRFVVWEAALYVLTCPREVMAAQLDRLAGLIGMDTVEISVLPLGAQLRRAPGHGFWIYDRRRVIVETINTEMWLDDEESVALYERAWDLMAEAAVQGPQARRLIGRARASLGLE
>NZ_CP010833.1|WP_075265202.1|3777271_3778375_-|methyltransferase-domain-containing-protein
MSSAPQASTYPDLVRDLADRGLLNGRWLQVFEAVPRSRFVPAAVWRQFPDRCEPVMGTEAWLALVNSDEPVVTQLDDGAEGGPGVATSSNSMPSMVARMLGLLDIEDGQRVLEIGTGTGYVAALLCERLGDDLVHSVELDPVVARQAAEALAQSGYRPQLRVGDGEQPWPGLGLVDRLIATCALRYVPYALLRQVRPGGIVVAPLAREFWSGAMVRLRVQDDGTAVGPFCGGATYMPMRSHRVPDLHGVQGKGRARAAGLDPAELLDLGFALFAGARLPGVRLIHQDTEEGVQVWVTRENGSAATAATGDEVWQYGPGFLWEEIEQTWWEYETAGRPDAGQFGLTVTDRRQQVWLRDPSEIIRPCRT
>NZ_CP010833.1|WP_010063058.1|3775909_3776338_+|nucleoside-deaminase
MRRALAEAARAASAGDVPVGAVVLGPDGTELATGHNEREATGDPTAHAEILALRRAAEAVGEWRLTDCTLVVTLEPCTMCAGALVQSRVARVVYGARDEKAGAAGSLWDVIRDRRLNHRPEVIAGVLEPECAEQLTAFFRTL
>NZ_CP010833.1|WP_010063059.1|3775203_3775755_+|hypothetical-protein
MYFAALLARTEDGWEASDTELDDVETLSDLTDLAREASVDEDTVLVYIEQEDAWFGVVRVDGEEDPRIYVSDASAAARSSYGEILLTDEMLGREPGAEDEIAALEELVDLDGTEDGEPERTAPAADTDDDAPDPDAVPAGPIGELGVLADLGMSEKELLTLQTDALAEIAEAVGAAEVLESVR
>NZ_CP010833.1|WP_075268418.1|3774658_3774910_+|hypothetical-protein
MADGDLRDNPAARGPREGRDAEGMAGATGDVEDAQESDAARRRRRAQFLRELHEAKQLRDRVQPRRARAARMRQQMRMRTFRW
>NZ_CP010833.1|WP_010063062.1|3773920_3774556_-|uracil-phosphoribosyltransferase
MRIHVVDHPLVAHKLTTLRDKRTDSPTFRRLADELVTLLAYEATRDVRTEQVDIETPVTPTTGVKLSHPRPLVVPILRAGLGMLDGMVRLLPTAEVGFLGMIRNEETLQAETYATRMPEDLSGRQVYVLDPMLATGGTLVAAIQELIKRGADDVTAVVLLAAPEGVEVMERELAGTPVTVVTASVDERLNEHGYIVPGLGDAGDRMYGTAE
>NZ_CP010833.1|WP_075265201.1|3773226_3773829_+|LytR-C-terminal-domain-containing-protein
MGGKYRITGDTYPRMRRPRHRRRLVLAGIGAVVVLGLVGWGSLQLIEVFTGGDKSASAADHKRDCPTAKPSVAPAKALPKPAAIKVNVYNATTRTGLAKAAAEELKKRGFTIGEVGNAPKEYDKKVPGAGVLLGAPAAKNGSFTVLGTQLAGTVQKTDTRKTGEVDLILGAKFKAFSTPKEATAAMAALTKPTPAPSPSC
>NZ_CP010833.1|WP_003967677.1|3772746_3773043_+|type-II-toxin-antitoxin-system-VapB-family-antitoxin
MIFKRIGNGKPYPDHGRESTRQWADVAPRPVRLDQLVTTKGQLDLETLLAEDSTFYGDLFAHVVKWQGDLYLEDGLHRAVRAALQQRQVLHARVLDLG
>NZ_CP010833.1|WP_075265207.1|3782997_3783489_+|hypothetical-protein
METNGGRPTPEQAQSALAEAEQIQASAAVLSATPWPNWFFATLTLYIAVVPIVYGGVMADEDWLLPSPAWTGIMLAITALYLGLFALAAKTWREKTGVALRLDVLPKRATVPLAVGLPSILVGAAFAFRFTGSPVWLFAASVIGAAASVGFHLAFVRLHRASA
>NZ_CP010833.1|WP_107472872.1|3783506_3783806_+|helix-turn-helix-domain-containing-protein
MPAGFDATIHAPNRLRICALLDTAGEAEFGLVQKQLGLSASVLSKHATVLMDAGYVEQRKAVRDTRQRVWLRLTRAGRDAYQGHLAALRAIVGPADPAS
>NZ_CP010833.1|WP_075265209.1|3784421_3784715_+|Dabb-family-protein
MIRHLVLFKLNDGVERDEPRVVAGDRAFRELEGQIPELEFWECAWNITDRPIAYDYAINSAVADEDALKRYIEHPAHQAAAGQWREFATWVIADYPF
>NZ_CP010833.1|WP_075265210.1|3784923_3785811_+|RNA-polymerase-sigma-factor-SigF
MPASTAPQVPPQSVQASPAVPPVPAEDIQTETPDPSARPARARGADTRALTQVLFGQLKNLEPGTPEHRRVRAALIEANLPLVRYAAARFRSRNEPMEDVVQVGTIGLINAIDRFDPERGVQFPTFAMPTVVGEIKRYFRDNVRTVHVPRRLHELWVQVTGATEDLTTAHGRSPTTAEIAERLRISEDEVLACIEAGRSYHATSLEAAQEGDGLPGLLDRLGYEDPALAGVEHRDLVRHLLVQLPEREQRILLLRYYSNLTQSQISAELGVSQMHVSRLLARSFARLRSANRIEA
>NZ_CP010833.1|WP_030579030.1|3786045_3786912_+|RNA-polymerase-sigma-factor-SigF
MSEEQGSSKVLTLTKSVPAPAVLTSSPEAIDTRTLSRSLFLRLAALGPASGPEGTDSPERTYVRDTLIELNLPLVRYAAARFRSRNEPMEDIVQVGTIGLIKAIDRFDCERGVEFPTFAMPTVVGEIKRFFRDTSWSVRVPRRLQELRLALTKTSDELAQKLDRSPTVPELARALGVSEEDVVDGLAVGNAYTASSLDSPSPEDDGGEGSLADRLGYEDTALEGVEYRESLKPLLAKLAPRERQIIMLRFFANMTQSQIGEEVGISQMHVSRLLTRTLAQLREGLIAD
>NZ_CP010833.1|WP_075265211.1|3787002_3787848_+|hypothetical-protein
MRRQTYGFTGRRGTAIAASAAALCLGTGLLSGCGSGPGDGYTAVGAAAGSSKPPADGAPSGDVTLTPLDGSDKGGGGGTSPGPGTSPSAGSPGDGRSGDAQDGSGGARTATPPGGRQAAGSSGGPGEAPSQPAGPSTPSKPGGSGGAGSPPGDSTGNPSPPGPGSPGTPSSPKPPDPPATPAALTLSAPQRAAADKRWCEKVTVEFRNTGGSAARSGTVTFATHIIGALGVDWATITSSQPLPAPIGAGSTRSKTYTVCVESWRVPLGMRVETQDVSAVWE
>NZ_CP010833.1|WP_075265212.1|3787867_3788083_-|hypothetical-protein
MAHNPHAPQPGPEGNHDPAGSTQMFRAFVDEGEPQRRQQPAATSSGPRVGVIAAVIAVVAVLGAVAWLALS
>NZ_CP010833.1|WP_069737694.1|3788364_3788877_+|MarR-family-transcriptional-regulator
MAARSSYEELARQLSAVGAVKRGLARALPPECPAGSAAVLTLLDRHGEMRISRLAELLSVDMSVTSRHVAHVADRGWIERSADPADKRSRILRLTPGGHAQLDELTRRTTEVFAHNLQDWSDDDVGRLIALLSRLRDSFACRGSGGCVPGRHTGECRTGLGDEAHARTPV
>NZ_CP010833.1|WP_075265213.1|3788908_3791440_+|MFS-transporter
MATTTPTGVRGGHAKHGGHGGGNASGAPDGTPMTHRQIMEALTGLLLGMFVAILSSTVVSNALPEIISDLGGGQSAYTWVVTASLLAMTATTPLWGKLADLFSKKLLVQIALVIYVLGSVVAGLSTSSGMLIACRVIQGIGVGGLSALAQIVMAAMIAPRERGRYSGYLGAVFAVATVGGPLLGGVITDTSWMGWRWCFYVGVPFAVIALIVLQKTLKLPVVKREGVKVDWSGAFFISAAVSLLLVWVTFAGDKYDWLSWQTYVMVAGSVLLGLIFVFIESRAKEPIIPLRLFRNRTITLASIASLFVGIAMFAGTVFFSQYFQLARGKSPTMSGVMTIPMIAGLFLSSTISGQVITKTGRWKAWLVTGGFLVTAGLGLLGTIRYDTPYWHVAVFMFVMGLGIGMMMQNLVLATQNQVAPEDLGSASSVVTFFRSLGGAIGVSALGAVLGNRVTQYVKDGLAALGPEGAKLGHGGTGGGGIPDLDKLPEPFRLVMESAYGHGVGDVFLYAAPCALVAFIVTIFIKEVALKTSAANDAPTEASDQAPAPAAVETAELPVPATVGAAGLVSEGAAGVTSVDTAEAPQDTVQGTPVHGVVRGAEGAPVARAAVTLISLGGRQLGRSVARTDGGYTLDAPGSGSYVLIASADGFQPQASTVVVGDEPLAFDILLSGTSGLAGTVRAAESGAPVDGAMVIVTDVRGDVLATGASGPTGEFAFGELIPGSVTVAVNAAGFRPLALPVEIGGQGVTRVEAALRSGALVRGTVRAGSARGPLGDARVTLIDAAGNVVATATTGEDGAYAFTDLDAGEYAVIATGYPPVAGSLTVSGTGVDGHDIELAHPGE
>NZ_CP010833.1|WP_032776631.1|3791741_3792560_+|hypothetical-protein
MGLRAQVRTRDGWAVQHAVVTVTDMTGAQVLRAAADEDGTVRTDGALTAGAYTVIVTAVGYAPAASTALVTASGRIEAGQIVLARQGGVELPPPGAWSLDPAHSSVGAVAQHLGISSVHGRFTDFGGRIEIAEEINSSRVDAVIRAASIDTGNGMRDKHLRSPDFLDVDRYPEIAYSSTALAPAGPDRWTVHGELTMHGVSRPVDLDLTYLGTGPDPWGGVRAAFHATAELRRDDFAMNYNQVVQAGISAIGTTLRVELDIQAVQGEALPMA

Crispr_ID: NZ_CP010833_12

• CRISPR_ID: NZ_CP010833_12
• CRISPR_location: 4115422-4115831
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 10 spacers

Consensus repeat of NZ_CP010833_12

Consensus_repeat	Method
GGGGCCNTCGCCGGTGTNGG	CRT

spacers of NZ_CP010833_12

>12.1|4115442|19|NZ_CP010833|CRT
TCGGTGTGGTGGTTCGGTT
>12.2|4115481|19|NZ_CP010833|CRT
AGGCGGCGGCGATGACGTT
>12.3|4115520|19|NZ_CP010833|CRT
TCGGTGTGGTGGTTCGGTT
>12.4|4115559|19|NZ_CP010833|CRT
AGGCGGCGGCGATGACGTT
>12.5|4115598|19|NZ_CP010833|CRT
TCGGTGTGGTGGTTCGGTT
>12.6|4115637|19|NZ_CP010833|CRT
AGGCGGCGGCGATGACGTT
>12.7|4115676|19|NZ_CP010833|CRT
TCGGTGTGGTGGTTCGGTT
>12.8|4115715|19|NZ_CP010833|CRT
AGGCGGCGGTGATGACGTT
>12.9|4115754|19|NZ_CP010833|CRT
TCGGTGTGGTGGTTCGGTT
>12.10|4115793|19|NZ_CP010833|CRT
AGGGGGCGGCGATGACGTT

CRISPR arrays and Neighbor proteins around NZ_CP010833_12

CRISPR arrays

The CRISPR arrays of NZ_CP010833_12

>merge|NZ_CP010833|12|4115422-4115831|CRT
GGGGCCTTCGCCGGTGTCGGTCGGTGTGGTGGTTCGGTTGGGGCCCTCGCCGGTGTTGGAGGCGGCGGCGATGACGTTGGGGCCTTCGCCGGTGTCGGTCGGTGTGGTGGTTCGGTTGGGGCCCTCGCCGGTGTTGGAGGCGGCGGCGATGACGTTGGGGCCTTCGCCGGTGTCGGTCGGTGTGGTGGTTCGGTTGGGGCCCTCGCCGGTGTTGGAGGCGGCGGCGATGACGTTGGGGCCTTCGCCGGTGTCGGTCGGTGTGGTGGTTCGGTTGGGGCCCTCGCCGGTGTTGGAGGCGGCGGTGATGACGTTGGGGCCTTCGCCGGTGTCGGTCGGTGTGGTGGTTCGGTTGGGGCCCTCGCCGGTGTCGGAGGGGGCGGCGATGACGTTCGGGCCCTCGCCGGTGTCCG

>NZ_CP010833|12|2|4115422-4115831|CRT
GGGGCCTTCGCCGGTGTCGG	TCGGTGTGGTGGTTCGGTT
GGGGCCCTCGCCGGTGTTGG	AGGCGGCGGCGATGACGTT
GGGGCCTTCGCCGGTGTCGG	TCGGTGTGGTGGTTCGGTT
GGGGCCCTCGCCGGTGTTGG	AGGCGGCGGCGATGACGTT
GGGGCCTTCGCCGGTGTCGG	TCGGTGTGGTGGTTCGGTT
GGGGCCCTCGCCGGTGTTGG	AGGCGGCGGCGATGACGTT
GGGGCCTTCGCCGGTGTCGG	TCGGTGTGGTGGTTCGGTT
GGGGCCCTCGCCGGTGTTGG	AGGCGGCGGTGATGACGTT
GGGGCCTTCGCCGGTGTCGG	TCGGTGTGGTGGTTCGGTT
GGGGCCCTCGCCGGTGTCGG	AGGGGGCGGCGATGACGTT
CGGGCCCTCGCCGGTGTCCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075265416.1|4112224_4115287_+|AfsR/SARP-family-transcriptional-regulator	unknown	unknown	gnl|CDD|276938
NZ_CP010833.1|WP_075265425.1|4124324_4125416_+|hypothetical-protein	unknown	unknown	gnl|CDD|367900
NZ_CP010833.1|WP_075265414.1|4105081_4108687_+|cobaltochelatase-subunit-CobN	unknown	unknown	gnl|CDD|235663
NZ_CP010833.1|WP_075265418.1|4116213_4117212_-|hypothetical-protein	unknown	unknown	gnl|CDD|235010
NZ_CP010833.1|WP_079181494.1|4100349_4101117_+|cobalt-precorrin-6A-reductase	unknown	unknown	gnl|CDD|236144
NZ_CP010833.1|WP_075265413.1|4103410_4104715_-|cobalamin-biosynthesis-protein-CobG	unknown	unknown	gnl|CDD|274131
NZ_CP010833.1|WP_075265412.1|4102734_4103361_-|precorrin-8X-methylmutase	unknown	unknown	gnl|CDD|181352
NZ_CP010833.1|WP_075265415.1|4108777_4109896_+|DUF4037-domain-containing-protein	unknown	unknown	gnl|CDD|379078
NZ_CP010833.1|WP_075265409.1|4099213_4100323_-|cobalt-precorrin-5B-(C(1))-methyltransferase	unknown	unknown	gnl|CDD|234615
NZ_CP010833.1|WP_075265426.1|4125394_4126639_+|acyl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173847
NZ_CP010833.1|WP_075265420.1|4118637_4119618_+|cysteine-synthase-family-protein	unknown	unknown	gnl|CDD|107204
NZ_CP010833.1|WP_075265423.1|4121632_4122460_+|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|369571
NZ_CP010833.1|WP_075265419.1|4117208_4117448_-|4-oxalocrotonate-tautomerase-family-protein	unknown	unknown	gnl|CDD|224853
NZ_CP010833.1|WP_075265408.1|4098544_4099159_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265411.1|4101217_4102732_-|precorrin-2-C(20)-methyltransferase	unknown	unknown	gnl|CDD|381173
NZ_CP010833.1|WP_075265424.1|4122468_4124328_+|asparagine-synthase-(glutamine-hydrolyzing)	unknown	unknown	gnl|CDD|273676
NZ_CP010833.1|WP_075268438.1|4117913_4118504_+|serine-acetyltransferase	unknown	unknown	gnl|CDD|200082
NZ_CP010833.1|WP_075268437.1|4109989_4111789_-|protein-lysine-6-oxidase	unknown	unknown	gnl|CDD|366506
NZ_CP010833.1|WP_075265422.1|4120300_4121251_+|DMT-family-transporter	unknown	unknown	gnl|CDD|223769
NZ_CP010833.1|WP_075268439.1|4126635_4128096_+|dihydroorotase-family-protein	unknown	unknown	gnl|CDD|223122

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075265416.1|4112224_4115287_+|AfsR/SARP-family-transcriptional-regulator	gnl|CDD|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	5.19517e-39
NZ_CP010833.1|WP_075265425.1|4124324_4125416_+|hypothetical-protein	gnl|CDD|367900	pfam04303, PrpF, PrpF protein. PrpF is a protein found in the 2-methylcitrate pathway. It is structurally similar to DAP epimerase and proline racemase. This protein is likely to acts to isomerise trans-aconitate to cis-aconitate.	5.78365e-22
NZ_CP010833.1|WP_075265414.1|4105081_4108687_+|cobaltochelatase-subunit-CobN	gnl|CDD|235663	PRK05989, cobN, cobaltochelatase subunit CobN; Reviewed.	0
NZ_CP010833.1|WP_075265418.1|4116213_4117212_-|hypothetical-protein	gnl|CDD|235010	PRK02186, PRK02186, argininosuccinate lyase; Provisional.	5.54553e-06
NZ_CP010833.1|WP_079181494.1|4100349_4101117_+|cobalt-precorrin-6A-reductase	gnl|CDD|236144	PRK08057, PRK08057, cobalt-precorrin-6x reductase; Reviewed.	1.03639e-106
NZ_CP010833.1|WP_075265413.1|4103410_4104715_-|cobalamin-biosynthesis-protein-CobG	gnl|CDD|274131	TIGR02435, Precorrin-3B_synthase, precorrin-3B synthase. An iron-sulfur protein. An oxygen atom from dioxygen is incorporated into the macrocycle at C-20. In the aerobic cobalamin biosythesis pathway, four enzymes are involved in the conversion of precorrin-3A to precorrin-6A. The first of the four steps is carried out by EC 1.14.13.83, precorrin-3B synthase (CobG), yielding precorrin-3B as the product. This is followed by three methylation reactions, which introduce a methyl group at C-17 (CobJ; EC 2.1.1.131), C-11 (CobM; EC 2.1.1.133) and C-1 (CobF; EC 2.1.1.152) of the macrocycle, giving rise to precorrin-4, precorrin-5 and precorrin-6A, respectively. [Biosynthesis of cofactors, prosthetic groups, and carriers, Heme, porphyrin, and cobalamin].	1.0005e-52
NZ_CP010833.1|WP_075265415.1|4108777_4109896_+|DUF4037-domain-containing-protein	gnl|CDD|379078	pfam13228, DUF4037, Domain of unknown function (DUF4037). This presumed domain is functionally uncharacterized. This domain family is found in bacteria and eukaryotes, and is approximately 100 amino acids in length. There is a single completely conserved residue P that may be functionally important.	1.02352e-36
NZ_CP010833.1|WP_075265409.1|4099213_4100323_-|cobalt-precorrin-5B-(C(1))-methyltransferase	gnl|CDD|234615	PRK00075, cbiD, cobalt-precorrin-6A synthase; Reviewed.	1.81841e-154
NZ_CP010833.1|WP_075265426.1|4125394_4126639_+|acyl-CoA-dehydrogenase	gnl|CDD|173847	cd01158, SCAD_SBCAD, Short chain acyl-CoA dehydrogenases and eukaryotic short/branched chain acyl-CoA dehydrogenases. Short chain acyl-CoA dehydrogenase (SCAD). SCAD is a mitochondrial beta-oxidation enzyme. It catalyzes the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of SCAD is reoxidized in the oxidative half-reaction by electron-transferring flavoprotein (ETF), from which the electrons are transferred to the mitochondrial respiratory chain coupled with ATP synthesis. This subgroup also contains the eukaryotic short/branched chain acyl-CoA dehydrogenase(SBCAD), the bacterial butyryl-CoA dehydorgenase(BCAD) and 2-methylbutyryl-CoA dehydrogenase, which is involved in isoleucine catabolism. These enzymes are homotetramers.	3.74643e-62
NZ_CP010833.1|WP_075265420.1|4118637_4119618_+|cysteine-synthase-family-protein	gnl|CDD|107204	cd01561, CBS_like, CBS_like: This subgroup includes Cystathionine beta-synthase (CBS) and Cysteine synthase. CBS is a unique heme-containing enzyme that catalyzes a pyridoxal 5'-phosphate (PLP)-dependent condensation of serine and homocysteine to give cystathionine. Deficiency of CBS leads to homocystinuria, an inherited disease of sulfur metabolism characterized by increased levels of the toxic metabolite homocysteine. Cysteine synthase on the other hand catalyzes the last step of cysteine biosynthesis. This subgroup also includes an O-Phosphoserine sulfhydrylase found in hyperthermophilic archaea which produces L-cysteine from sulfide and the more thermostable O-phospho-L-serine.	5.78717e-137
NZ_CP010833.1|WP_075265423.1|4121632_4122460_+|cupin-domain-containing-protein	gnl|CDD|369571	pfam07883, Cupin_2, Cupin domain. This family represents the conserved barrel domain of the 'cupin' superfamily ('cupa' is the Latin term for a small barrel).	3.18992e-10
NZ_CP010833.1|WP_075265419.1|4117208_4117448_-|4-oxalocrotonate-tautomerase-family-protein	gnl|CDD|224853	COG1942, COG1942, Uncharacterized protein, 4-oxalocrotonate tautomerase homolog [General function prediction only].	3.09675e-14
NZ_CP010833.1|WP_075265412.1|4102734_4103361_-|precorrin-8X-methylmutase	gnl|CDD|181352	PRK08285, cobH, precorrin-8X methylmutase; Reviewed.	7.67157e-131
NZ_CP010833.1|WP_075265411.1|4101217_4102732_-|precorrin-2-C(20)-methyltransferase	gnl|CDD|381173	cd11646, Precorrin_3B_C17_MT, Precorrin-3B C(17)-methyltransferase (also named CobJ or CbiH). Precorrin-3B C(17)-methyltransferase participates in the pathway toward the biosynthesis of cobalamin (vitamin B12). There are two distinct cobalamin biosynthetic pathways. The aerobic pathway requires oxygen, and cobalt is inserted late in the pathway; the anaerobic pathway does not require oxygen, and cobalt insertion is the first committed step towards cobalamin synthesis. This model includes CobJ of the aerobic pathway and CbiH of the anaerobic pathway, both as stand-alone enzymes and when CobJ or CbiH form part of bifunctional enzymes, such as in Mycobacterium tuberculosis CobIJ where CobJ fuses with a precorrin-2 C(20)-methyltransferase domain, or Bacillus megaterium CbiH60, where CbiH is fused to a nitrite and sulfite reductase-like domain. In the aerobic pathway, once CobG has generated precorrin-3b, CobJ catalyzes the methylation of precorrin-3b at C-17 to form precorrin-4 (the extruded methylated C-20 fragment is left attached as an acyl group at C-1). In the corresponding anaerobic pathway, CbiH carries out this ring contraction, using cobalt-precorrin-3b as a substrate to generate a tetramethylated delta-lactone.	7.00577e-116
NZ_CP010833.1|WP_075265424.1|4122468_4124328_+|asparagine-synthase-(glutamine-hydrolyzing)	gnl|CDD|273676	TIGR01536, Asparagine_synthetase_1, asparagine synthase (glutamine-hydrolyzing). This model describes the glutamine-hydrolysing asparagine synthase. A poorly conserved C-terminal extension was removed from the model. Bacterial members of the family tend to have a long, poorly conserved insert lacking from archaeal and eukaryotic sequences. Multiple isozymes have been demonstrated, such as in Bacillus subtilis. Long-branch members of the phylogenetic tree (which typically were also second or third candidate members from their genomes) were removed from the seed alignment and score below trusted cutoff. [Amino acid biosynthesis, Aspartate family].	3.02993e-103
NZ_CP010833.1|WP_075268438.1|4117913_4118504_+|serine-acetyltransferase	gnl|CDD|200082	TIGR01172, Serine_acetyltransferase, serine O-acetyltransferase. Cysteine biosynthesis [Amino acid biosynthesis, Serine family].	2.3268e-58
NZ_CP010833.1|WP_075268437.1|4109989_4111789_-|protein-lysine-6-oxidase	gnl|CDD|366506	pfam01186, Lysyl_oxidase, Lysyl oxidase.	4.6325e-15
NZ_CP010833.1|WP_075265422.1|4120300_4121251_+|DMT-family-transporter	gnl|CDD|223769	COG0697, RhaT, Permeases of the drug/metabolite transporter (DMT) superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / General function prediction only].	3.58111e-21
NZ_CP010833.1|WP_075268439.1|4126635_4128096_+|dihydroorotase-family-protein	gnl|CDD|223122	COG0044, PyrC, Dihydroorotase and related cyclic amidohydrolases [Nucleotide transport and metabolism].	5.11412e-126

Protein sequences

>NZ_CP010833.1|WP_075265416.1|4112224_4115287_+|AfsR/SARP-family-transcriptional-regulator
MNELAESGRVQFRILGSFECWDGNDRIRVGGPVHEKVLVTLLLEPQRVLPVFRLVEAAWDENAPATAAHQVRKAVAELRQRIPGGRELIVTEGPGYRILAEPAQVDLGRFTEGLKQAREAAVAGQSSAAIATLREALALWRGPLLSGTGGSVLSAASAALEERRLTAVEQLFDLRLAVGESSEIIGELREFIDAHPLRETLRGQLMLALFRTGRQADALEEFAKIRDHLIEELGIGPGDALSELHNAVLRNSPELAAPQPPAAAPFTPEGNPSTLPYDLRDFTGREAEVSELLGFVEEASGSGPLIVAIDGMGGSGKTSLAVRAAHRLAEKYPDAQLYIDLRGFTPNGRPMSAGAAAEALLRMLGVPADRIPEDAEGRIALWRRTMSTHRMILLLDNVMDDSQVRPLLTSPTETLVLVTSRALLVDLDAAHTVSLGVMPPGDSVALVEGVLGRSRAENEPEAVAQLTELCGHLPLALRIAAARLRKRPRWTVRYLVDRLRDDAHRLAELNSGERSVEVTLRLSYEGLAAETREAFRLLGQYPGAEINTYAAGALLGIGPREAEKVLEYLLDMHLLQQHETGHYAFHDLVRSFAQNLSRSGARRQPEAGGEQHATAGGDDEIMHAVGRLLDFALAATDAACDLLFPGRARIGGAGPPAWVAELPPLETVEQARDWLEREQDSLLAIVSLAYRWEMDRHVGLLTANVVFPLDLRGRLEEFRELGRVAVAASRRLGDAALLRLSLSNLSVACWKLGRLTEGITMSEEALALSIGLDDRRGEAKDTGVLGLLLSTLGRYDEALPRLQQSIDIKRQLGAERAEAESLTNLSSLYAEWGRYPEAVEAATRSITLSRSIGSVDKEVEGLTDLAVARIGLGEIAAASELLALARKLAGETMSPADLSLVLALSAEVADRLGESVQAAEWGESALSLGDLSGVPMREAAVGNIIGRFHTRNGRYSAAFELHARARDAASRIGYRVEEARALAGMADALDRMGEEQAASIHRESAREAFDAMGVPTPRAA
>NZ_CP010833.1|WP_075268437.1|4109989_4111789_-|protein-lysine-6-oxidase
MTRSPQGRTNRLTRPSVAIAAAVAVTAGVVAAAPDAKTAEPSPKLSLIAATTSVTLDSWKEDPGVYLDLGTYLTSENGAFELKVTRKSYKDPVLAAQVLRNGKKTTTKALPAGLVKDFSGLPDFAQISVTDAAGKTVLKQTEAFCPNNASGRVRPDAPANSKYPQSCPVNPFTLGSVWGVENGWASNTYAGYYAKPVQLAAGTYTAKISVTKKYRDLFGIANKPQTVKVTVRERSWEEEEQGGDAAARSAAPRSAKSAAGHQGHGGHEGHQQAADAPAASAHAAHGAPARPEAPAARTTGATPTFNVGHGPYPPAPPALPWALKKESLQRQAFSAAKVGDRPGQTDGSRQAPAAEPNAKRPTGKATVPDVPKPDLRSLPAYGITVSDGYEDAPGKDYLAFSANVWNAGPAKLVVDGFRSPGKKLMDAYQYFYDAKGKQVGYTPTGTMEWDPRPGHEHWHFTDFASYRLLKADKKESVRSGKEAFCLANTDAVDYTVKNANWHPDNTDLSTACGQENSISVREVLDVGSGDTYTQDLPGQSFDITGLPNGTYYIQVLANPENRLKETDYKNNSALRKVVLGGKKGARTVKVPAHDLVNAN
>NZ_CP010833.1|WP_075265415.1|4108777_4109896_+|DUF4037-domain-containing-protein
MTTPARAFLPGLELSRILYEEAVRPILDAELPGLRYAAARVGPGSEVLGFDTARSADHEWGPRLDLFLEPADANAHGERIHRLLAERLPKQVRGWPTHFRHADPADPVGHMELTDGPVDHRVGVRVAGGWLHGQLGLRRPAAPGGDLPELTVRDWLAVPQQKLAEVTGGAVFHDGVGTLTRAREALAWYPDQVWRYLLACQWQRIAQEEAFVGRCAEVGDDLGSAVVAGRSVRDLMRLCLLLEREYAPYSKWLGSAFARLPRAGELLLSLRGAVTAGDYATRERHLCDAYERVAAAQNRTGLTEVVDPARRPYHDRPFQVLHAERFARALARTVTDPELRDLPLTGAVDQWADSTDFLGRPEAVRAAVEALG
>NZ_CP010833.1|WP_075265414.1|4105081_4108687_+|cobaltochelatase-subunit-CobN
MILLLSTSDTDLLSARASEGPVSYRYANPSRVDLGGLPELLDGVDLVVVRLLGGVRAWQEGLDAVLATGRPVVVLTGEQAPDAQLMAASTVPIGIAAEAHAYLAHGGPANLEQLARFLSDTVLLTGHGFEPPAPAPAWGPLEREARAVPEGAPTVAVLYYRAHHMSGNTAFVDALCTAVEDAGARPLPLYVASLRTPETELIDALRAADAIVTTVLAAGGTKPAEASAGGDDESWDAGALTQLDVPILQALCLTSPRTAWEENDEGVSPLDAATQIAVPEFDGRLITVPFSFKEIDEDGLPAYVPDAERAARVAGIAVRHAKLRNIPNAEKRIALVLSAYPTKHSRIGNAVGLDTPASAVALLRRLRAEGYDFGPEEDIPGLVSGDGDELIYALIEAGGHDQEWLTEEQLAKNPVRIPAADYRRWFAELPQELRESVEEHWGPAPGGMFVDRSANPEGDIVLAALRRGNLLILIQPPRGFGENPIAIYHDPDLPPSHHYLAAYRWIAASAEDNGFGADAMIHLGKHGNLEWLPGKNAGLSAACGPDAALGDLPLVYPFLVNDPGEGTQAKRRVHATLIDHLVPPMARADSYGDIARLEQLLDEHAQIAAMDPAKLPAIRAQIWTLIQAAKLDHDLGVEDRPEDEGFDDFIMHLDGWLCEIKDVQIRDGLHVLGNPPAGNDRVNLVLAVLRARQIWGGTASLPGLREALGLDESAATRTAADEIEEQARALVQAMDDADWAPAAVATVAAGLPEAVADILTFAATEVVPRMAATTDELTHAVHALNGGFVPAGPSGSPLRGLVNVLPTGRNFYSVDPKAVPSKLAWETGQALAESLLTRYRTDNGDWPTSVGLSLWGTSAMRTAGDDIAEAFALLGIRPVWDDASRRVTGLEPIPYAELGRPRIDVTLRISGFFRDAFPHTVGLLDDAVRLAASLDEPAERNYVRAHTQADLAEHGDERRATTRIFGSRPGTYGAGLLQLIDSRDWRTDADLAEVYTVWGGFAYGRELDGRPAREEMESAYKRIEVAAKNTDTREHDIADSDDYFQYHGGMVATVRALKGTAPEAYIGDSTRPETVRTRTLVEETSRVFRARVVNPKWIEAMRRHGYKGAFELAATVDYLFGYDATTGVVADWMYDKLTQTYVLDPENKQFLQEANPWALHGIAERLLEAESRGMWAKPDPAVLEALRQVYLETEGNLEGED
>NZ_CP010833.1|WP_075265413.1|4103410_4104715_-|cobalamin-biosynthesis-protein-CobG
MLAAMPDSAPSPLSAGGPALRGSGDACPGTLRLHRADDGALARVRVPGGVLSADRADALLTAAGRFGDGELHLTSRGNIQLRGLGAECGGGLAELLTAAGLLPSAAHERARNIVASPLAGLDGSPALGHLLAELDGLVCGSAAAASLSGRFLFALDDGRGDVDALGADVTLIAAGDRCLLRIGAADEVFRVPSGEGPRAALLAAEAFLRAARDAGAWRVKDLPDDVQAGVRADVRAELIRTVRAAAGPAVHRPRPRTATPPAPGAHGSPNAISVDVPLGRLTPAQWRLLTETARRYGNELRLTPWRGIVVPGPFAHDEAVEALRTLDAAGLISAPDSPWTGVGACIGHPGCAKSLSDVRAEAGAAVGPVGRLPVYWSGCERRCGHPHGEWIDVVATPDGHRISHVRGERRDPRTTVRNGDPARLAAAVAEARAL
>NZ_CP010833.1|WP_075265412.1|4102734_4103361_-|precorrin-8X-methylmutase
MHQYEKDGPAIYRQSFATIRAEADLAGLPADVSQVAVRMIHACGMVDLVKDLAFSPNAVADARAALRAGAPILCDVAMVASGVTRKRLPADNDVVCTLSDPSVPELAAKMGTTRSAAALELWRDRMEGAVIAVGNAPTALFRLLEMIEEGAPRPAAVIGVPVGFVGAMESKEALAEHPSGLEHLIVRGRRGGSAIAAAALNAIASEEE
>NZ_CP010833.1|WP_075265411.1|4101217_4102732_-|precorrin-2-C(20)-methyltransferase
MSESSGSTGRLYGVGLGPGDPNLMTLRAVQAIGEADVVAYHSARHGRSIARSIAAAHLRPDHIEEALVYPVTTETTDHPGGYRGALEEFYEAAAARLAAHLDAGRTVAVLAEGDPMFYGSYMHMHKRLADRYATEVIPGVTSVSAAAARLGTPLVEGEEILTILPGTLPEEELTARLTATDTAVVMKLGRTFPAVRGAFEASGRLPEARYVERATMAGERTGELADIEPESVPYFSVAVLPSRIDASRPSGRAAGEVVVVGTGPAGPLWLTPETRGALAAADALVGYTTYLDRVPVRPGQARHGSDNKVESERAEFALDLARRGHRVAVVSGGDPGVFAMATAVLEVASQDAYADIPVRVLPGVTAANAAAARAGAPLGHDYATISLSDRLKPWEVIAERLRAAASADLVLALYNPGSKSRTWQVGQARDLLLEHRSPDTPVVLARDVGGPAESVRTVRLADVDPAEVDMRTLLIVGSSQTRWVKRGEGGGRDIVWTPRRYPEA
>NZ_CP010833.1|WP_079181494.1|4100349_4101117_+|cobalt-precorrin-6A-reductase
MPVSAVHVLVLGGTTEARRLAESLAGDRSVRVTTSLAGRVAAPRLPPGEVRVGGFGGPEGLAAWMREHDVDALIDATHPFAAAMSRNAAEAAALARVPLLALCRPGWVAQDGDRWHSAGSLAEAAGLLPALGERVFLTTGRMGLAAFEGAGLDALWFLVRSVDAPEPPCPARMEVLLDRGPFDLDGERELLRRHRIDVLVTKDSGGDATAPKLTAAREAGIPVVVVRRPPVPEGVPVARTPDEAARWVVRLHASG
>NZ_CP010833.1|WP_075265409.1|4099213_4100323_-|cobalt-precorrin-5B-(C(1))-methyltransferase
MNAETQGGRSAQLKHTGLRPGWTTGACATAATTAAYTALLTGDFPDPVSITLPKGQTPAFALAVEELAPGQASAGVVKDAGDDPDVTHGALVRATVRRLPPGSGVVFRAGSGVGTVTLPGLPLEVGEPAVNPVPRRLMREHVERVAAEHGAAGDVEITVSVDHGEEIARSTWNGRLGILGGLSILGTTGVVVPYSCSAWIDSIRRGVDVARAAGLTHVAGCTGSTSERTVRAEHDLPDIALLDMGDFAGAVLKYVRRHPVDRLTICGGFAKLSKLAAGHLDLHSARSQVDKAFLADLARRGGADEDLATRITSANTGLEALRLCEAAGVPLGDLVAARARDEALSVLRGAPVAVDVLCIDRAGVVVGRG
>NZ_CP010833.1|WP_075265408.1|4098544_4099159_+|hypothetical-protein
MLIEGYGHGPVVAGESLVGRRGFWASHLLAMCADGTCAGQADPEWFGGDGADADALAEVLFDPEQWLVFRVPVPDGHPVPGVVVVYRNLVDEFGVDYLPGAPGTGACLSSGPVSGLSWQELTRVADCPRPPAEGVQDASGRFLLLLPLLSGEWSDEVVRERIVAALVAVGAPEDSVGRAAGHLLGHLERRALHDAGWGSPLSGG
>NZ_CP010833.1|WP_075265418.1|4116213_4117212_-|hypothetical-protein
MTVPTGSGTADPRRLLLVAPSRRLAAAAEEAGFHVVTVPDTTGFTEEELRAHLRETVLTQRVGRLIACGDASTHPAVLEAAEELGVSPNPASAARLLADAAEVRNLLNRSGPQWQALALPDEPGHRPPLCDVGYGVETLTVEGMHRVTGIVEFRRDDGGFGDRGERGAGHGPDGADRGGTTPPGSGPAVHTFPAPITGAEEAEIRALATGLLDLVGYEFGYAFTRIARTGRGPQIVDAVPRQASWPVSRLIELTTGLVAERELVQALSGKPLKAAVPVGCAAALPLSDPPGAPGRITAPGDVREARDGYVVLTALTPTELATRRAAVLGCPT
>NZ_CP010833.1|WP_075265419.1|4117208_4117448_-|4-oxalocrotonate-tautomerase-family-protein
MPVISVDWWKGNDRAQRQELVEELTACVSRIAGCPEDAVTVIVRDVETDHWGKGGVLADALLAGAVSRPGPQDTGGQQP
>NZ_CP010833.1|WP_075268438.1|4117913_4118504_+|serine-acetyltransferase
MLAALREDLAVVVARDPSVRGGKEAILHPALTALWAHRVAHRLHGRGLRIPARLLARWARRVTAVEIHPGAVLGRRVFIDHGAGVVIGETAVVGDDVTMYHQVTLGAVGWWSDNKRPEGDRRHPVVGSGVILGANATVLGPVTVGDRAVIGAQALVNKDVPGGARVLAPTAVIKEPGRRPELMEDVFTVIASAGSW
>NZ_CP010833.1|WP_075265420.1|4118637_4119618_+|cysteine-synthase-family-protein
MTTTAHAPLTSVAPARPAVASRIEDLVGSTPLLELRLRDLAPGARVLAKLESANPMSSSKDRAALYMLRAAEERGALRPGGTVIEATSGNTGISLAAFAASRGYRCVIVLPDNATAERVRLLRAFGAEIVQTPSSLGYPGAIAEAERLHAATPDSWFPCQHENLDNVRAHYETTGPEIQAAVSSLGRRVAAFVCGVGTGGTLTGVARALKEHDPDVRVIAVEPEKSPILSKGYAGQHRIPGLNGGFVADTTDVSLIDEVVTVSDEDALLTARRLATGQGLFAGVSSGAAAYASERVAQRPELSDGIVVTLLPDTGERYLSMWEDQA
>NZ_CP010833.1|WP_075265422.1|4120300_4121251_+|DMT-family-transporter
MNLANWGRFGLLAALWGCSFAFIKMSLEAFAPLQLASGRLVVGALVVAAMLALKRLPLPGRPLWGHIAVASVFGNVIPFTLFAIGEQHTTATIAGVIQGATPLITMGVAALALSEEKPTRRKVIGLVGGFVGLIIVVGPWNTDGFGSIGGQLACVGAAASYAVSFVYIRRFIGPHKLPALSVTAAQLGMASVITVVLTTFVTGWSLHGDLTAKPLLALLVLGAASTGIAFALLNRLIADAGPTTASGVNYLVPVFSVVVGVLALGEPMSWNVPVGGVLVIAALALAEGRISSLSRAGKPKPTSPVAPDRVPEKSRP
>NZ_CP010833.1|WP_075265423.1|4121632_4122460_+|cupin-domain-containing-protein
MTRTTTSPSPSAPSLGDARIISTGDFVFTPLAGRLTEIATPVSPAAGSTHVTLHVVRIAPGETFSPESSADEENTAVVFDGRGTATVGSRGRSVERAHAAYAPTGQALSLTADEDGLTVYIWRTPLTPGRRPGTSPEPFSTLWDETTQLRGFGGTGQIAPDADRATMNFVFWPGNGSSQLCLHCGIQQPGQTFNVHLHPDSDEAFIAFEGIGQMYLRDRWIDVAAGDVLYAAPGVLHGARNPHTGPDARRFVTCGGPSPYDPALYSAAGLSSDVR
>NZ_CP010833.1|WP_075265424.1|4122468_4124328_+|asparagine-synthase-(glutamine-hydrolyzing)
MCRIHGSFHARTTDDEMRRVAALQHHGGPDAQSFARQSGWALGNNRLSIMDPEGGDQPYRLGDITVVFNGEIYNHDRLRTELMRQGFHFDDRCDGSILPALYLTYGDRFAEHLDGMFSVAVMDLRREPRLVIATDASGMKPLYYHWDERSDQFHFASELPALLGFDGVRPYEDELGLHTYLSAKTPFGQRTMFEGIDVLPPATTAVVTREDGLRLTSRRMGYESAPPVDEDRSLSRAGESLRELLSREVSRLLVADAPVAAITSGGLDSSLVTALAARILFDRGSSEALHTFNIAYTGNWPGDERAFASEVSRHTGTVHHQVEIDPATFPDLMGDVVRHLGQPNADPITLSTFSLFRAVRDAGFKVALTGDAADELFGGYSRMTQALAAPEGADWAGPYLDHLAAVPQSLRRQLYTPEYAARVLAPGASPLPPGLTDVLAHGEGSRLQRITRIEQRYRLPAYHLRRVDHLSMASSVEARLPFCQPSVVRFAASLPDQHRTVPGVGVKRALYRAAEGLLPASVLNRPKQPFTLPITAMLAPGQRLWAMARDVLSPQALRADGRLRYEVVDALFAEQEARPSDGTSLALWALMSHQMWRSEFFGPSAGAHRGTRELAVMAG
>NZ_CP010833.1|WP_075265425.1|4124324_4125416_+|hypothetical-protein
MIVSLVKATGAPCPTAVLDGRDLPESDPQLLSALADLRADLTLQGSADVLKNAIVRPSRHPLFDLDYRFVQSLPQSPDSFDLRGSCGHSILAAVEAAARTGMIQPLVPGCRVRVNVLNNGDNVVCEAEETSGGGTRFTAHFLCSPPLELPELLMTGEPVTYVPFEGRSVPVSLVSMGNPYAFVDATQLGVDGPDALFGDDPALFDTMTRLRVAVCASQGWETFGAFPKIAAVLPQDGGGLYVRAVSVPSWHPTVALTGAICLGAAAGITGTVPWSLAGSAARDPDALLQVRTPGGCVRVAAHSTSGPDGRRELAWVSVAEKQVEYRGLLPRPRSANGLQPSAGPRLTPTAPLPEENSWVPLTA
>NZ_CP010833.1|WP_075265426.1|4125394_4126639_+|acyl-CoA-dehydrogenase
MGSADSLTAVRDDIGSGALSDPFTVDPFPGSHRGAARDVTAPPAPLLPAPPVLARLAACAEAADLSGEPDREAVAVLRESGLLALVVPECYGGAGADAVALNTCVEQVASVNASAAIMLFQHCAVTSRIVENGSPAQHREVLPRLADGRWLAASAWSESGAGADKKNLATRAHRTPEGDWLLDGAKSFTTSAGLADVYLVLAQTPDEAPAAASSRDTGYGAAGQTFFLVPGDHPGLVPDTSMRLTGMRGSATGFVSVHACVVPDSARLGATGIAASIIGRVRDSGASLGAVAVGLAQAALDAAHAHAERRGLYAHQAVRHRLVDLATEVESARAVVERAGRRTAADPGMATLHSKLAASAAAERVVADVARFLGSAGYVETHPINRFGRDARAVALMGPTNDLCKELVSLPWNR
>NZ_CP010833.1|WP_075268439.1|4126635_4128096_+|dihydroorotase-family-protein
MNSSSRISSDSSPADLVVEGGRLVTPDGVTEGSVVVRDGRVAAIVAPGAPLPAGPRLSAAGRYVLPGLIDSHVHFRTPGLEHKETWENGSRAALAGGVTTVMDMPNTRPPSLDEATLREKAALIAGRSYVDHRFHMGADPDHPEVLADLAPEVATSAKAFMAGHHTAPVVFREAHQLEAAFAAAARGGVRLVLHAEDQHVFDLLDSRAGDPESYDAYEPHRPRSGAIVAVAKVVQLVRTYGTKTHILHVSSAEETDLLVAAAAEGLPISFEVTGHHLAFTDHDTALRGPRTRLSPAIRAPRDRDRLWQAVLSGEASTIGSDHAPHTVEEKNRPPAEAPPGLPGVQELAVSVWTGMLARGIAPDDAAVHLTRLMGTGPADLFDLAGKGRLAVGSDADLALLDPAARWQLSASHVASLCGWSAYEGWMFTGRFTTVVRGGNVVWDLERGTLGEPLGRWLGGPAPSEQALPTARIPASEPARELEGATR

Crispr_ID: NZ_CP010833_13

• CRISPR_ID: NZ_CP010833_13
• CRISPR_location: 4698724-4698809
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_CP010833_13

Consensus_repeat	Method
CGGCTGACCCCGTACGCGCCGGGGCC	CRISPRCasFinder

spacers of NZ_CP010833_13

>13.1|4698750|34|NZ_CP010833|CRISPRCasFinder
TGCGTTCTTCCGCCGCCCACCGCCGCCTTGATGG

CRISPR arrays and Neighbor proteins around NZ_CP010833_13

CRISPR arrays

The CRISPR arrays of NZ_CP010833_13

>merge|NZ_CP010833|13|4698724-4698809|CRISPRCasFinder
CGGCTGACCCCGTACGCGCCGGGGCCTGCGTTCTTCCGCCGCCCACCGCCGCCTTGATGGCGGCTGACCCCGTACGTGCCGGGGCC

>NZ_CP010833|13|12|4698724-4698809|CRISPRCasFinder
CGGCTGACCCCGTACGCGCCGGGGCC	TGCGTTCTTCCGCCGCCCACCGCCGCCTTGATGG
CGGCTGACCCCGTACGTGCCGGGGCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075265815.1|4710860_4711634_+|Rieske-(2Fe-2S)-protein	unknown	unknown	gnl|CDD|239550
NZ_CP010833.1|WP_032766835.1|4700313_4701315_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|235640
NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_CP010833.1|WP_079181509.1|4690399_4691608_-|MFS-transporter	unknown	unknown	gnl|CDD|340882
NZ_CP010833.1|WP_075268491.1|4698814_4699840_-|DUF4243-domain-containing-protein	unknown	unknown	gnl|CDD|372882
NZ_CP010833.1|WP_075268488.1|4687598_4687976_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265805.1|4689135_4690356_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|238045
NZ_CP010833.1|WP_075265814.1|4707928_4710256_+|molybdopterin-oxidoreductase-family-protein	unknown	unknown	gnl|CDD|239155
NZ_CP010833.1|WP_159027439.1|4686420_4687383_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_107472812.1|4702607_4704200_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075265812.1|4705202_4706294_-|P1-family-peptidase	unknown	unknown	gnl|CDD|239070
NZ_CP010833.1|WP_075265806.1|4691851_4693126_+|acyl--CoA-ligase	unknown	unknown	gnl|CDD|223395
NZ_CP010833.1|WP_075265808.1|4694656_4695367_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_075265813.1|4706822_4707932_+|MFS-transporter	unknown	unknown	unknown
NZ_CP010833.1|WP_010059620.1|4710261_4710864_+|4Fe-4S-binding-protein	unknown	unknown	gnl|CDD|319891
NZ_CP010833.1|WP_075265811.1|4704214_4704970_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075268490.1|4695592_4697125_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075268487.1|4682914_4686295_+|ATP-binding-protein	unknown	unknown	gnl|CDD|224400
NZ_CP010833.1|WP_075265807.1|4693112_4694390_-|M6-family-metalloprotease-domain-containing-protein	unknown	unknown	gnl|CDD|274507
NZ_CP010833.1|WP_075265809.1|4697167_4697680_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	4.1e-55	182.2	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075265815.1|4710860_4711634_+|Rieske-(2Fe-2S)-protein	gnl|CDD|239550	cd03467, Rieske, Rieske domain; a [2Fe-2S] cluster binding domain commonly found in Rieske non-heme iron oxygenase (RO) systems such as naphthalene and biphenyl dioxygenases, as well as in plant/cyanobacterial chloroplast b6f and mitochondrial cytochrome bc(1) complexes. The Rieske domain can be divided into two subdomains, with an incomplete six-stranded, antiparallel beta-barrel at one end, and an iron-sulfur cluster binding subdomain at the other. The Rieske iron-sulfur center contains a [2Fe-2S] cluster, which is involved in electron transfer, and is liganded to two histidine and two cysteine residues present in conserved sequences called Rieske motifs. In RO systems, the N-terminal Rieske domain of the alpha subunit acts as an electron shuttle that accepts electrons from a reductase or ferredoxin component and transfers them to the mononuclear iron in the alpha subunit C-terminal domain to be used for catalysis.	2.65332e-20
NZ_CP010833.1|WP_032766835.1|4700313_4701315_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|235640	PRK05901, PRK05901, RNA polymerase sigma factor; Provisional.	4.74687e-114
NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	2.14827e-50
NZ_CP010833.1|WP_079181509.1|4690399_4691608_-|MFS-transporter	gnl|CDD|340882	cd17324, MFS_NepI_like, Purine ribonucleoside efflux pump NepI and similar transporters of the Major Facilitator Superfamily. This family is composed of purine efflux pumps such as Escherichia coli NepI and Bacillus subtilis PbuE, sugar efflux transporters such as Corynebacterium glutamicum arabinose efflux permease, multidrug resistance (MDR) transporters such as Streptomyces lividans chloramphenicol resistance protein (CmlR), and similar proteins. NepI and PbuE are involved in the efflux of purine ribonucleosides such as guanosine, adenosine and inosine, as well as purine bases like guanine, adenine, and hypoxanthine, and purine base analogs. They play a role in the maintenance of cellular purine base pools, as well as in protecting the cells and conferring resistance against toxic purine base analogs such as 6-mercaptopurine. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The NepI-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.0158e-49
NZ_CP010833.1|WP_075268491.1|4698814_4699840_-|DUF4243-domain-containing-protein	gnl|CDD|372882	pfam14027, DUF4243, Protein of unknown function (DUF4243). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and eukaryotes. Proteins in this family are typically between 348 and 477 amino acids in length.	6.32418e-13
NZ_CP010833.1|WP_075265808.1|4694656_4695367_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	8.52204e-08
NZ_CP010833.1|WP_075265805.1|4689135_4690356_+|helix-turn-helix-domain-containing-protein	gnl|CDD|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	2.12877e-09
NZ_CP010833.1|WP_075265814.1|4707928_4710256_+|molybdopterin-oxidoreductase-family-protein	gnl|CDD|239155	cd02754, MopB_Nitrate-R-NapA-like, Nitrate reductases, NapA (Nitrate-R-NapA), NasA, and NarB catalyze the reduction of nitrate to nitrite. Monomeric Nas is located in the cytoplasm and participates in nitrogen assimilation. Dimeric Nap is located in the periplasm and is coupled to quinol oxidation via a membrane-anchored tetraheme cytochrome. Members of the MopB_Nitrate-R-NapA CD belong to the molybdopterin_binding (MopB) superfamily of proteins.	0
NZ_CP010833.1|WP_107472812.1|4702607_4704200_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.05953e-68
NZ_CP010833.1|WP_075265812.1|4705202_4706294_-|P1-family-peptidase	gnl|CDD|239070	cd02252, nylC_like, nylC-like family; composed of proteins with similarity to Flavobacterium endo-type 6-aminohexanoate-oligomer hydrolase (EIII), the product of the nylon oligomer degradation gene, nylC. EIII is an amide hydrolase that catalyzes the degradation of highly-polymerized 6-aminohexanoate oligomers. Together with other nylon degradation enzymes, such as 6-aminohexanoate cyclic dimer hydrolase (EI) and 6-aminohexanoate dimer hydrolase (EII), EIII plays a role in the detoxification and biological removal of the synthetic by-products of nylon manufacture. EIII shows sequence similarity to L-aminopeptidase D-amidase/D-esterase (DmpA), an aminopeptidase that releases N-terminal D and L amino acids from peptide substrates. Like DmpA, EIII undergoes autocatalytic cleavage in front of a nucleophile to form a heterodimer. DmpA shows similarity in catalytic mechanism to N-terminal nucleophile (Ntn) hydrolases, which are enzymes that catalyze the cleavage of amide bonds through the nucleophilic attack of the side chain of an N-terminal serine, threonine, or cysteine.	5.7322e-92
NZ_CP010833.1|WP_075265806.1|4691851_4693126_+|acyl--CoA-ligase	gnl|CDD|223395	COG0318, CaiC, Acyl-CoA synthetases (AMP-forming)/AMP-acid ligases II [Lipid metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	2.72159e-50
NZ_CP010833.1|WP_010059620.1|4710261_4710864_+|4Fe-4S-binding-protein	gnl|CDD|319891	cd16369, DMSOR_beta_like, uncharacterized subfamily of DMSO Reductase beta subunit family. This family consists of the small beta iron-sulfur (FeS) subunit of the DMSO Reductase (DMSOR) family. Members of this family also contain a large, periplasmic molybdenum-containing alpha subunit and may have a small gamma subunit as well. Examples of heterodimeric members with alpha and beta subunits include arsenite oxidase, and tungsten-containing formate dehydrogenase (FDH-T) while heterotrimeric members containing alpha, beta, and gamma subunits include formate dehydrogenase-N (FDH-N), and nitrate reductase (NarGHI). The beta subunit contains four Fe4/S4 and/or Fe3/S4 clusters which transfer the electrons from the alpha subunit to a hydrophobic integral membrane protein, presumably a cytochrome containing two b-type heme groups. The reducing equivalents are then transferred to menaquinone, which finally reduces the electron-accepting enzyme system.	2.31489e-100
NZ_CP010833.1|WP_075268490.1|4695592_4697125_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.73283e-69
NZ_CP010833.1|WP_075268487.1|4682914_4686295_+|ATP-binding-protein	gnl|CDD|224400	COG1483, COG1483, Predicted ATPase (AAA+ superfamily) [General function prediction only].	1.84962e-63
NZ_CP010833.1|WP_075265807.1|4693112_4694390_-|M6-family-metalloprotease-domain-containing-protein	gnl|CDD|274507	TIGR03296, hypothetical_protein, M6 family metalloprotease domain. This model describes a metalloproteinase domain, with a characteristic HExxH motif. Examples of this domain are found in proteins in the family of immune inhibitor A, which cleaves antibacterial peptides, and in other, only distantly related proteases. This model is built to be broader and more inclusive than pfam05547.	1.26424e-53
NZ_CP010833.1|WP_075265809.1|4697167_4697680_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	5.97915e-14

Protein sequences

>NZ_CP010833.1|WP_075265809.1|4697167_4697680_-|MarR-family-transcriptional-regulator
MESMTTASTSAPRWLSDEEQRVWRAYLHATTLLEDHFDRQLQRDAGMPHIYYGLLVQLSQAPRRRMRMTELARNAKITRSRLSHAIARLEKNGWVRREDCPSDKRGQNAVLTDDGLDMLRRSAPGHVEAVRQAMFDRLTDEQVRSLGEIMRTLATGLEPEGADADLPWLR
>NZ_CP010833.1|WP_075268490.1|4695592_4697125_+|MFS-transporter
MSRTADTALPDPSRWRALAFIALAQLMVVLDATIVNIALPSAQTDLGISDGNKQWVITAYALAFGGLLLFGGRIADLWGRKRTFVVGLIGFALASALGGAAQNEAMMFGSRALQGVFGALLAPAALSLLAVMFTDAKERAKAFGIYGAIAGGGGAVGLILGGFLTEYLNWRWTFFVNIPFAVVAAVGAYFVIREPSGTRNRAPLDIPGVVLSTLGLVALVYGFTRAESAGWSDSLTVSMFIAAAVLLLAFVVTEARVKSPLLPLRVLTERNRGGVYLSLGLAIIAMFGLFLFLTYYLQVVKGYSPVKTGFAFLPMIAGMITGSTQIGTRLMTRVPPRLLMGPGFLVAAVGMLLLTQLDLNTSYAAVILPGMLLLGLGMGTAFMPAMSLATHGIEPRDAGVASAMVNTSQQVGGAIGTALLNTIAASATTAYVADHAARATDPKLLELQAMVSGFAAAIWWAVGILVAAAVIAIALINTGRPGTGQGGTESASGEGAEGAEDEFRIPVVAH
>NZ_CP010833.1|WP_075265808.1|4694656_4695367_+|TetR/AcrR-family-transcriptional-regulator
MKSVAKAVAQAVTGSAAQAVAGKGAAPAGSCRVARPRADALRNRERIVSAARELFVESGPDVPLDDVARRAGVGNATLYRNFPDRAALTHEVVLAVTSRTTLRAEEAVAAESDPFAALSRFVHAAADERIGALCPMISGVFDKDHPDLLAERDRLEEAVAGLVSRAQSAGRLRTDIAVGDVLVALSQLTRPLPGIACQGIDRFTHRHLQLFLDGLETPARSELPGSAATLEDLRRP
>NZ_CP010833.1|WP_075265807.1|4693112_4694390_-|M6-family-metalloprotease-domain-containing-protein
MQQPRHRIRRHRRPVALAGATALVIAAMASASTTLHSGGRASAGPAATAQDSALAPCRISATMGVQMSEGLPTPPGYARSTGEIRALNLMIDFPDAEGTEPATDRFAEFFPQTSDWFRTSSYGRLVYRPEAPVKDWLRMPMAFTEYGIERGSPFEPGYRQLVKDIVAAADPRVDFSEYDLVNILVSPNAGPSALDTVLSVTFSGNDEAPEADGVPLANTSFVYSRQDDGSGSYAETGYRVLPHENGHVFGLPDLYTMEGGGSVGHWDIMSEDWGANNDFLAWHKWKLGWLDNEQISCASQPGVSEHTLGPLATEGGTKLAFVPLSAQSGYAVEVRTAAGNDEAVCRPGVLIYKVSSDVDTGQGPVSVADATEDSGGCTRRPNVHAELSDAPFRPGQTFTDRANGVRISVLDEDDDGNYRVRVTRP
>NZ_CP010833.1|WP_075265806.1|4691851_4693126_+|acyl--CoA-ligase
MPHTVPPPEPEAAVSAEFARRAARVETSLTAPGAPFAAVLGERGAPEYADGPRTLREFVETTWAYGEAPFLIAGERACSYGEFFAAASALAVRLREGYGLHPGDRAVIASGNRPEWQIAFWAAQLAGLVAVPLDAGWAEDAFTYVLEDCEPGVLLVDGERLERVAGWARRTGTRVVLFPGSGDESASGPRVEFPGGDQAADGLRVERYEDFPAPDPLAAPPDVEPRPEDDATILYTSGATGRLRGAVATHLAQAGAALNARYHAAASARARGAIPGLEPVPVSLMAAPFSDAAAFTGFYGAMAGGGALALKDDAAAGAGPVGYDLAETCGVVLAPIGDDRRAESGGAGRPAPVTEVRIAGPSGEELPDGEPGELWLRGQSLFRGYWRDAAATGAAFADGGWFRTGDRAVRRDGWVSVVGRLTGA
>NZ_CP010833.1|WP_079181509.1|4690399_4691608_-|MFS-transporter
MTSVVPSAAPPAAPSRSGLGRPAALAFAGAGALTVSNIYFPQPLLDAIASGLDVSGPAASLIATAAQVGYALGIALVVPLADAARLRRLATTLLLLTTAGLLVAAAAPNLATLTVATLALSTTTVLPQILVPTAASLAGPGHSGRAVGAIGIGITLGSTLSRTLSGAVAGLSGDWRTAYLVAAALTGGLVFVLPRLLPASRDGRSVPYRELIGSLPRLVRAHPGLRFSAFLGATVFAAFSAFWATLAFHLAGPPFDRGVAWAGLFGLFGLPAALLSYTAGRLSDRRGPRYVNTVALVCVSAAFLVLGVGGDSLTALVIGTNLLVYGTSSSQVANQVRVFRLGEQVRARLNTLFMLASFTGGSVGSLTGAALYAHWGWTGMVLGCGGFLLPAAVALARGRHLG
>NZ_CP010833.1|WP_075265805.1|4689135_4690356_+|helix-turn-helix-domain-containing-protein
MLEQPHFGRRLKQLRSERGLSQAALAGEGMSTGYVSRLESGARQPTARAAQHLASRLGIGVAAFEEESPADSLAQALATAASATSDTTLEALERVLYPGEGQDPLLRWQGLWLVAQGRRQHSDHARERVVLEELVALGDELGLPALRARGLTQLARCLRAGGEIVPAVEAATAAHALARDHDLPVPDVAAGLLALVSAESEAGRLTEARAHADELTALNVPRSEPLGAEALWTAAAVRVRQGDLDAAQKLLEEALDGFAGAEDLTLWTRLRVAAARLHLQKSPPEPDASERYAEQAETGMVFVGIPALEQEVTSIKAEISFHRGQFADARVLLDRVCAADPRMTYRNRVRLEVLDSRLLVIEGREQEGLERMRALAEEAQAAASIDLAADIWRLLAETLAAARAMP
>NZ_CP010833.1|WP_075268488.1|4687598_4687976_+|hypothetical-protein
MEVYTTGATVVAVVGSFVTAAIAQYAAASGRRMRTLRTAEHLASQFRRNWVSILSATLLIAGVCLLATVLDVTEGDSGGVHWMVEAALILGVARSYRLLWLFNAVIMATDRDLAERASDSSQLRT
>NZ_CP010833.1|WP_159027439.1|4686420_4687383_+|hypothetical-protein
MAVRNRDRTVHFYEIADAKEPASRMGPRDWAAELRQLRDLPLAQRTVDSAGETLIGAVDPLQPAPHLLVAKVRKDKPQQINFDDGSFSYLQLAANKGLIDVTTVYFLSFGNVVATMGGGISAPRVRAIQRWFNGMHLIGEEIALRPVVDARSRDKLARASAVEKVTIRVLPEPHDSPSALRSSSDIGTALSRMHEEYPDMTITLTLEVPRKPRWYSLRRRARGHRQLLDSTSALASDISDWLDNTDAVDTARAVAHIEEWDQQATDEKIDFVAERITAKCRVPLEATDGHSIDLHVALTELERVALEHERVLRAAVGADI
>NZ_CP010833.1|WP_075268487.1|4682914_4686295_+|ATP-binding-protein
MALSNRDRIGRMIELLSDGLLPLVEREMTKRQGEGWFGDAVAEEREKGRSLTSKRDPQFLLNLLQRYWGSYFRHFLPGATRGYASEVNDVRNRWAHNEPFSADDTVRALDTAERLFTSVGATADLVEQVRKSRINLQRDMIEVETKRQTRRAAAMPSIAAEGLKSWRDVLVPHQDVARGDFNASEFAANLAEVAKGEGAPEYTDPEEFFQRTYLTEGLRDLLGKSLRRISGDNNASPTVNLQTNFGGGKTHSMLALYHLYSSGLQPQRLPQEMQELIAASPSGLPQEEVRRAVLVGTALAPGQPHEKVDGTKVNTLWGELAWQLGGRRAYDVIAEADKTRTSPGSELLQDLLAAYAPCLILIDEWVVYARQLVSNDDLAAGTFETHFSFAQSLTEAVEAVAGAQLVLSIPASEDGKDDKGDTDEIGGEAGQIALDRLQKVIHRKADAWRPASSDESFEIVRRRLFETPSGAVQAEINKVARLFSQFYGTYKRDFPAGVDGTDYERRIKSTYPIHPELFSRLYEDWSTLDRFQRTRGVLRLMSAVIHALWRDQNKSPMIMPGDIPLDDQRVASELTHYLEDRWKPIIDADVDGPDSTPVSVDNEKTVLGQRAMSRRIARTVFMGSAPTIKAAKKGLSEPYIRLGMAIPGDALGNFRTALNTLADRSTYLYSDADRYWYDTHANITRTAKDEAERLIGRDDDVWAEIVRRLSPIQHRRGDFGAVHIAPQHTKEVPDLDQARLVLLHPKYVHRGGKDIPDTPALEFAAEALSSHGTRNRKHQNTLVFLAPDKKDMGDLMEAAREYLGWKKVLDRQMELDLTESQRRQAQTRRDQANEKVELRVGDAYRWALIPEQDAGAPIVWEHLKVDGGRADDAAVRTADRLRREGLLYLQQAPALLYQKLSGPLSRIWEQDGHISVGRLWELHTAYPYMNRLVNRLVLDQGVEDVLSMVTWETEGFALASGYDENDGCYQGLVLPSGNAKFGQITDATLLVRPDAAIRQRQQAEEEAAQKREAASGISSSKSEEPAPTGGISSVGTTRPPTSQGQPVIPKVPTRFYATAQLTPEQYSKNASKYVFEILQPLDVIGTEVEITIEIQAKRPDGFAEDKVRVLTENANTLKLKAEFEVE
>NZ_CP010833.1|WP_075268491.1|4698814_4699840_-|DUF4243-domain-containing-protein
MDDTTGTLDEALERIHLSGPERDGWLSNHAPMAVEALVRHGQASAVHRWLDRYGPKLEEMPDGTGSPVTARNWREALGDPRRIADWTGYFDRETAERPWRDVLVEWWPRLLPGIAAGATHAVIRVGHSVRTLLAGEETAPRVRELAHALGYWAARHQPLSVPALLGPAPSAAAALDRVPLVPEQSGGIRDRFAQLTAFPEWPAREAASAEAARSALRELVRASTHRYATHAHGEPIMLVHAATAPNAVLRTLPALPGELWEPSLRASWAASAAVTAAYAPREAAPAPASATGAADAGELFARAAAHGDDHTIKFTDTALDVGDALAFSAARRAIELNPPVF
>NZ_CP010833.1|WP_032766835.1|4700313_4701315_+|sigma-70-family-RNA-polymerase-sigma-factor
MATRAVARRTSAASGETDRASSVRAVGGEIADRDLVGMYLDEIARTPLLDAAKEVDLSQTIEAGVYAQQILDGEVESDAGDAKREELEALVADGERAKDIFIRSNLRLVVAVARRYPRAGLPLLDLIQEGNAGLVRAVEKFDYAKGFKFSTYATWWIRQAITRSIADQSRTIRLPVHLVEELGRIRRVQREFNREHGRDPEHAEIAAELDSNAERVGNVLDWARDPVSLNMSVDDDGDTQFGDLLEDTSAVSPEQSVMTLLRSEELEDLIGKLDNRTASIIKMRYGIEDGRERTLTEVGKQHGLTRERIRQIEKHALLELKRMAHDTGFDAAA
>NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator
MSDTPARLLKLLSLLQTPREWPGGELAERLDVSPRTIRRDVDRLRDLGYPVEASRGSVGGYRLVAGAAMPPLLLDDEEAVAIAVGLRAGAGHAIEGVDEASVRALAKLEQVLPSRLRHRVSVLQNATVPLTRGDGSTIDPRTLTTLASAATGRERLRFAYRSGDGTRTKRQVEPYRLVSTGQRWYLVAYDIGREDWRTFRVDRVGEPYATGARFTPRPLPVEGAGSDAGGGTGSEGGGGTGSGDAATFLARSMRRMQPELRLDVWFGGPAEFVAARLPAHLGAPEPDGEGGCRLRASCTDSLEWVALRLALVDCEFSVQGPPQLVAYLESLGARLTRAARPADRHRRPGDRHRPACPEQGERGEQG
>NZ_CP010833.1|WP_107472812.1|4702607_4704200_+|MFS-transporter
MPSSAPPPPAASQLAPPTSPGSVKTPIASVPVTAPVSVPAPADRRRWFALAIVMTAAFMDLVDVTIVNIAIPSITRETGASVSAIQWITAGYALAFAAGLITGGRLGDIYGRKRLFLIGIGGFTLASALCGFAPNPEILVAARILQGATAALMVPQVLSIVHATFPAHERGKVFGLFGAVVGLGAVSGPLLGALLTEWDLFGLGWRPIFLINLPVGIAGLILGAKFITESRAPKAVRLDLPGVALITLAMLMLIYPLTRGHELGWPLWGHLSMVGSLLVFAALVIHQRRKALTDGSPLIELSLFRVKSFAAGIAVQLTFGVGLGIFFLVWTLYMQMGLGWSVLRAGVTGIPFSVAVSVAAGISVQKLVPRFGRKVLQSGALLMIAGLLIYLWESEQYGMGISSWQMAVPLVVMGVGMGLIVAPLTDTVLSEVPKEHAGSASGLINTVQQMGTALGLGLVSVVFFGAVGDRPAPEAVGPAFVDAFQGALWWVAGVLSVIFLVMFALPARPRAHGEGDVNTEADANPKADAN
>NZ_CP010833.1|WP_075265811.1|4704214_4704970_-|hypothetical-protein
MSDPYETTEHHLDRLLRRALNSFDLPDSTVDRLGTALAHSSSLHSSHHSSVLHRETYRHTYLLADGSALTLWELVHSGGRDARSPRRHELYDDEGDARIAASRLAGSLSDSPAFGDEGMQEAPGDLEMLTVLMSAPPAPLPRTYAPDNSADHARRVLRRAENADRPGEERARLLRAAFAHHITQIFGRQCDVDGRPAGFTLYEHAFLLLDGSETSLWEVEHTATPDGRHMCEVYEDEHTARAAMESRTRIC
>NZ_CP010833.1|WP_075265812.1|4705202_4706294_-|P1-family-peptidase
MTHEDKAPELPSLLDALTDVAGIRVGHAEVAGAGAGALSGTTVVLAPEGGAVAAVDVRGGGPGTRETDALDPRNLVQRVDAVVLTGGSAFGLDTASGVMAWLEEQGRGVRVGPGPTQVVPVVPAAALFDLGRGGDWRARPDASTGRAAVEAAAATGPGEPFAEGSVGAGTGAVAGQLKGGIGTASVRLASGVTVAAVVAVNAAGSVVDPRTGVLFGEYGAGEPPVHPPAGVHAAAEQRLAQEREAMEAAGGGVPPFNTTIAVVATDADLTRAQAQKLAGTAHDGLARAVRPVHMLTDGDTVFTLATGQVPVEPGNPLAVNEILAAGADVLARAIVKAVRAARSVEGPGGTFLSYTELYGARMR
>NZ_CP010833.1|WP_075265813.1|4706822_4707932_+|MFS-transporter
MTEPSEATAAAEPPAPGEPAATPPAPTGPRSVTTRATLAGVVVSALLILAIVLGSRMLRNFDSALLPYAVATVFLAFGVAYRYTVWISAPGARRLFKQGWRSLFSVENFRRAPTALPRMIATYLGFQKFLGARSHARWAAHQLIFWGCVLAALITFPLTWGWFTFTSSTGSGPGYEMRIWGFKILGFDSLNLLGWLMFHGLDIAAVLVIPGASYFLWRRMKDRGAITGQRFAYDLVPLIALIVISVTGLLLTFSSVFLHGGGYQFLAILHMVSVVFTLIYIPFGKFFHIVQRPAAVGMQLFKYTGRKDDEVFACRRCEEPIDTGPYVENLRGTMRDLSLDFDAWAEYCPRCKRVLRGSAYLSHVKKGFK
>NZ_CP010833.1|WP_075265814.1|4707928_4710256_+|molybdopterin-oxidoreductase-family-protein
MTADPRAAADRRTFIPLDPSLAPPGTRAFRDAGGIPADRWHADQNGETLVPTHCCFCGVQCGMYLRVDHGGKVFGVEPRNHDINRMRLCPKGINAYQQVNHPDRLTAPLMRRSRDEEFREVSWGEALDFTVSEIKRIQQTYGNDAFGLLGGASLFSEKTYLVGKFARVALKSRHVDYNGRLCMVSAAGANKLAFGIDRAGNPFSDILLTDCLLIAGSNVGECFPVMTQYVWGARDRGATLIVVDPRETAIARTADIHVALKPGTDSAFFTSVLNVVIEEGLTDENFLADHATGWEELKAKAAEYPPSRAAAICGIPAEQIVQVARAFARAPKAMAWHARGIEHHSQGVENCLSVINLCAATGHIGKPGAGYGTITGQGNGQGGREHGQKSDLLPGGRSIMNEEHRRQICEIWGIEESELPPAGTSMMEMVWQMQRREIRGLIGICNNPFVSLPNYRVVKEGYDTTEFHAQFDFFLSETAANAHVVFPVTTWAEDEGVMANAEARVVKHNKAQDPPPGVRTDTWVICELARRLGAGDKFDFPDSRSVFDELRVASAGTVNDYYGITYERLEETGGIAWPCPATDHPGTPRLFEDGKTYHPDGRIHLQVVEWHPPMDPYDDEHPMSLTTGRTVAHFLSGNQTRRLGALVEQTPRPWAEIHPSHGFRNGEPVRIVTRRGSEVFPALVTEAIRPDTVFVPYHWPVPTAANALTIDALDPRSKIPEYKVCACRIEHAERIDEVPAPPVAPGHVAYPETQVSRTDPLPPTAPQGRGTSERS
>NZ_CP010833.1|WP_010059620.1|4710261_4710864_+|4Fe-4S-binding-protein
MMGRTIFIDPGRCIGCQACVSACRECDSHRGKSMIHLDYTDEGQSVASLPTVCMHCEDPVAPCAEVCPADAILVTADGVVQQADTTRCIGCSNCVNACPFGVPKIDLQAKLQMKCNLCYDRTAYGLAPMCATVCPTGALFYGTVEELQAERPGVQVADTFVFGETEVRTGVAMVVPAERVQWPVPGGLPVVEINGKDVRR
>NZ_CP010833.1|WP_075265815.1|4710860_4711634_+|Rieske-(2Fe-2S)-protein
MSVTDQQPGGEHPAGGDPREALQDRIAADSLTTRRDYLRIVTTVSGGLAVGGIGVAAGILHRHGDGEDGKAPEPKRIAGGLLPGESIAFRYPGEEDRAVAVRLDDGTLVGYSAVCTHLACAVLWRKDRGTEGELYCPCHEGVFDARSGEVTAGPPPRGLPKVVVVEQDDGSVWAVGTTRSGESIEEGLCRQLGGERPDLAARIGCPGIDGGAESPPRAAGPRTRNRTTGERPAPRAGGAPQATGVTSATVENPGGRA

Crispr_ID: NZ_CP010833_14

• CRISPR_ID: NZ_CP010833_14
• CRISPR_location: 4706395-4706489
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_CP010833_14

Consensus_repeat	Method
CCCCAAGCTCTCGGCTTCGCTCGAGCAGGG	CRISPRCasFinder

spacers of NZ_CP010833_14

>14.1|4706425|35|NZ_CP010833|CRISPRCasFinder
AGGGGCCCCTCCGGTGTTGTCGTCCATCACCACTT

CRISPR arrays and Neighbor proteins around NZ_CP010833_14

CRISPR arrays

The CRISPR arrays of NZ_CP010833_14

>merge|NZ_CP010833|14|4706395-4706489|CRISPRCasFinder
CCCCAAGCTCTCGGCTTCGCTCGAGCAGGGAGGGGCCCCTCCGGTGTTGTCGTCCATCACCACTTCCCCAAGCTCCCGGCTTCGCTCGAGCAGGG

>NZ_CP010833|14|13|4706395-4706489|CRISPRCasFinder
CCCCAAGCTCTCGGCTTCGCTCGAGCAGGG	AGGGGCCCCTCCGGTGTTGTCGTCCATCACCACTT
CCCCAAGCTCCCGGCTTCGCTCGAGCAGGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075265815.1|4710860_4711634_+|Rieske-(2Fe-2S)-protein	unknown	unknown	gnl|CDD|239550
NZ_CP010833.1|WP_075265819.1|4712972_4713491_-|hypothetical-protein	unknown	unknown	gnl|CDD|215257
NZ_CP010833.1|WP_032766835.1|4700313_4701315_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|235640
NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_CP010833.1|WP_075265814.1|4707928_4710256_+|molybdopterin-oxidoreductase-family-protein	unknown	unknown	gnl|CDD|239155
NZ_CP010833.1|WP_075268491.1|4698814_4699840_-|DUF4243-domain-containing-protein	unknown	unknown	gnl|CDD|372882
NZ_CP010833.1|WP_075268494.1|4713717_4714536_-|S-methyl-5'-thioadenosine-phosphorylase	unknown	unknown	gnl|CDD|236107
NZ_CP010833.1|WP_075265808.1|4694656_4695367_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_010059620.1|4710261_4710864_+|4Fe-4S-binding-protein	unknown	unknown	gnl|CDD|319891
NZ_CP010833.1|WP_075265817.1|4712087_4712309_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265810.1|4697947_4698730_+|dioxygenase	unknown	unknown	gnl|CDD|153375
NZ_CP010833.1|WP_032766860.1|4714743_4715085_-|FmdB-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225210
NZ_CP010833.1|WP_075265812.1|4705202_4706294_-|P1-family-peptidase	unknown	unknown	gnl|CDD|239070
NZ_CP010833.1|WP_075265818.1|4712325_4712859_-|large-conductance-mechanosensitive-channel-protein-MscL	unknown	unknown	gnl|CDD|376605
NZ_CP010833.1|WP_075265813.1|4706822_4707932_+|MFS-transporter	unknown	unknown	unknown
NZ_CP010833.1|WP_075265811.1|4704214_4704970_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075268490.1|4695592_4697125_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075265816.1|4711630_4712026_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_107472812.1|4702607_4704200_+|MFS-transporter	unknown	unknown	gnl|CDD|129794
NZ_CP010833.1|WP_075265809.1|4697167_4697680_-|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197670

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator	WYL	COG2378_WYL_CAS-I:CAS-III	4.1e-55	182.2	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075265815.1|4710860_4711634_+|Rieske-(2Fe-2S)-protein	gnl|CDD|239550	cd03467, Rieske, Rieske domain; a [2Fe-2S] cluster binding domain commonly found in Rieske non-heme iron oxygenase (RO) systems such as naphthalene and biphenyl dioxygenases, as well as in plant/cyanobacterial chloroplast b6f and mitochondrial cytochrome bc(1) complexes. The Rieske domain can be divided into two subdomains, with an incomplete six-stranded, antiparallel beta-barrel at one end, and an iron-sulfur cluster binding subdomain at the other. The Rieske iron-sulfur center contains a [2Fe-2S] cluster, which is involved in electron transfer, and is liganded to two histidine and two cysteine residues present in conserved sequences called Rieske motifs. In RO systems, the N-terminal Rieske domain of the alpha subunit acts as an electron shuttle that accepts electrons from a reductase or ferredoxin component and transfers them to the mononuclear iron in the alpha subunit C-terminal domain to be used for catalysis.	2.65332e-20
NZ_CP010833.1|WP_075265819.1|4712972_4713491_-|hypothetical-protein	gnl|CDD|215257	PLN02464, PLN02464, glycerol-3-phosphate dehydrogenase.	0.00364323
NZ_CP010833.1|WP_032766835.1|4700313_4701315_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|235640	PRK05901, PRK05901, RNA polymerase sigma factor; Provisional.	4.74687e-114
NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	2.14827e-50
NZ_CP010833.1|WP_075268491.1|4698814_4699840_-|DUF4243-domain-containing-protein	gnl|CDD|372882	pfam14027, DUF4243, Protein of unknown function (DUF4243). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and eukaryotes. Proteins in this family are typically between 348 and 477 amino acids in length.	6.32418e-13
NZ_CP010833.1|WP_075268494.1|4713717_4714536_-|S-methyl-5'-thioadenosine-phosphorylase	gnl|CDD|236107	PRK07823, PRK07823, S-methyl-5'-thioadenosine phosphorylase.	5.28085e-159
NZ_CP010833.1|WP_075265808.1|4694656_4695367_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	8.52204e-08
NZ_CP010833.1|WP_010059620.1|4710261_4710864_+|4Fe-4S-binding-protein	gnl|CDD|319891	cd16369, DMSOR_beta_like, uncharacterized subfamily of DMSO Reductase beta subunit family. This family consists of the small beta iron-sulfur (FeS) subunit of the DMSO Reductase (DMSOR) family. Members of this family also contain a large, periplasmic molybdenum-containing alpha subunit and may have a small gamma subunit as well. Examples of heterodimeric members with alpha and beta subunits include arsenite oxidase, and tungsten-containing formate dehydrogenase (FDH-T) while heterotrimeric members containing alpha, beta, and gamma subunits include formate dehydrogenase-N (FDH-N), and nitrate reductase (NarGHI). The beta subunit contains four Fe4/S4 and/or Fe3/S4 clusters which transfer the electrons from the alpha subunit to a hydrophobic integral membrane protein, presumably a cytochrome containing two b-type heme groups. The reducing equivalents are then transferred to menaquinone, which finally reduces the electron-accepting enzyme system.	2.31489e-100
NZ_CP010833.1|WP_075265810.1|4697947_4698730_+|dioxygenase	gnl|CDD|153375	cd07363, 45_DOPA_Dioxygenase, The Class III extradiol dioxygenase, 4,5-DOPA Dioxygenase, catalyzes the incorporation of both atoms of molecular oxygen into 4,5-dihydroxy-phenylalanine. This subfamily is composed of plant 4,5-DOPA Dioxygenase, the uncharacterized Escherichia coli protein Jw3007, and similar proteins. 4,5-DOPA Dioxygenase catalyzes the incorporation of both atoms of molecular oxygen into 4,5-dihydroxy-phenylalanine (4,5-DOPA). The reaction results in the opening of the cyclic ring between carbons 4 and 5 and producing an unstable seco-DOPA that rearranges to betalamic acid. 4,5-DOPA Dioxygenase is a key enzyme in the biosynthetic pathway of the plant pigment betalain. Homologs of DODA are present not only in betalain-producing plants but also in bacteria and archaea. This enzyme is a member of the class III extradiol dioxygenase family, a group of enzymes which use a non-heme Fe(II) to cleave aromatic rings between a hydroxylated carbon and an adjacent non-hydroxylated carbon.	1.29135e-103
NZ_CP010833.1|WP_032766860.1|4714743_4715085_-|FmdB-family-transcriptional-regulator	gnl|CDD|225210	COG2331, COG2331, Uncharacterized protein conserved in bacteria [Function unknown].	1.22142e-26
NZ_CP010833.1|WP_075265812.1|4705202_4706294_-|P1-family-peptidase	gnl|CDD|239070	cd02252, nylC_like, nylC-like family; composed of proteins with similarity to Flavobacterium endo-type 6-aminohexanoate-oligomer hydrolase (EIII), the product of the nylon oligomer degradation gene, nylC. EIII is an amide hydrolase that catalyzes the degradation of highly-polymerized 6-aminohexanoate oligomers. Together with other nylon degradation enzymes, such as 6-aminohexanoate cyclic dimer hydrolase (EI) and 6-aminohexanoate dimer hydrolase (EII), EIII plays a role in the detoxification and biological removal of the synthetic by-products of nylon manufacture. EIII shows sequence similarity to L-aminopeptidase D-amidase/D-esterase (DmpA), an aminopeptidase that releases N-terminal D and L amino acids from peptide substrates. Like DmpA, EIII undergoes autocatalytic cleavage in front of a nucleophile to form a heterodimer. DmpA shows similarity in catalytic mechanism to N-terminal nucleophile (Ntn) hydrolases, which are enzymes that catalyze the cleavage of amide bonds through the nucleophilic attack of the side chain of an N-terminal serine, threonine, or cysteine.	5.7322e-92
NZ_CP010833.1|WP_075265818.1|4712325_4712859_-|large-conductance-mechanosensitive-channel-protein-MscL	gnl|CDD|376605	pfam01741, MscL, Large-conductance mechanosensitive channel, MscL.	3.63042e-45
NZ_CP010833.1|WP_075268490.1|4695592_4697125_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.73283e-69
NZ_CP010833.1|WP_075265809.1|4697167_4697680_-|MarR-family-transcriptional-regulator	gnl|CDD|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	5.97915e-14
NZ_CP010833.1|WP_107472812.1|4702607_4704200_+|MFS-transporter	gnl|CDD|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.05953e-68
NZ_CP010833.1|WP_075265814.1|4707928_4710256_+|molybdopterin-oxidoreductase-family-protein	gnl|CDD|239155	cd02754, MopB_Nitrate-R-NapA-like, Nitrate reductases, NapA (Nitrate-R-NapA), NasA, and NarB catalyze the reduction of nitrate to nitrite. Monomeric Nas is located in the cytoplasm and participates in nitrogen assimilation. Dimeric Nap is located in the periplasm and is coupled to quinol oxidation via a membrane-anchored tetraheme cytochrome. Members of the MopB_Nitrate-R-NapA CD belong to the molybdopterin_binding (MopB) superfamily of proteins.	0

Protein sequences

>NZ_CP010833.1|WP_075265812.1|4705202_4706294_-|P1-family-peptidase
MTHEDKAPELPSLLDALTDVAGIRVGHAEVAGAGAGALSGTTVVLAPEGGAVAAVDVRGGGPGTRETDALDPRNLVQRVDAVVLTGGSAFGLDTASGVMAWLEEQGRGVRVGPGPTQVVPVVPAAALFDLGRGGDWRARPDASTGRAAVEAAAATGPGEPFAEGSVGAGTGAVAGQLKGGIGTASVRLASGVTVAAVVAVNAAGSVVDPRTGVLFGEYGAGEPPVHPPAGVHAAAEQRLAQEREAMEAAGGGVPPFNTTIAVVATDADLTRAQAQKLAGTAHDGLARAVRPVHMLTDGDTVFTLATGQVPVEPGNPLAVNEILAAGADVLARAIVKAVRAARSVEGPGGTFLSYTELYGARMR
>NZ_CP010833.1|WP_075265811.1|4704214_4704970_-|hypothetical-protein
MSDPYETTEHHLDRLLRRALNSFDLPDSTVDRLGTALAHSSSLHSSHHSSVLHRETYRHTYLLADGSALTLWELVHSGGRDARSPRRHELYDDEGDARIAASRLAGSLSDSPAFGDEGMQEAPGDLEMLTVLMSAPPAPLPRTYAPDNSADHARRVLRRAENADRPGEERARLLRAAFAHHITQIFGRQCDVDGRPAGFTLYEHAFLLLDGSETSLWEVEHTATPDGRHMCEVYEDEHTARAAMESRTRIC
>NZ_CP010833.1|WP_107472812.1|4702607_4704200_+|MFS-transporter
MPSSAPPPPAASQLAPPTSPGSVKTPIASVPVTAPVSVPAPADRRRWFALAIVMTAAFMDLVDVTIVNIAIPSITRETGASVSAIQWITAGYALAFAAGLITGGRLGDIYGRKRLFLIGIGGFTLASALCGFAPNPEILVAARILQGATAALMVPQVLSIVHATFPAHERGKVFGLFGAVVGLGAVSGPLLGALLTEWDLFGLGWRPIFLINLPVGIAGLILGAKFITESRAPKAVRLDLPGVALITLAMLMLIYPLTRGHELGWPLWGHLSMVGSLLVFAALVIHQRRKALTDGSPLIELSLFRVKSFAAGIAVQLTFGVGLGIFFLVWTLYMQMGLGWSVLRAGVTGIPFSVAVSVAAGISVQKLVPRFGRKVLQSGALLMIAGLLIYLWESEQYGMGISSWQMAVPLVVMGVGMGLIVAPLTDTVLSEVPKEHAGSASGLINTVQQMGTALGLGLVSVVFFGAVGDRPAPEAVGPAFVDAFQGALWWVAGVLSVIFLVMFALPARPRAHGEGDVNTEADANPKADAN
>NZ_CP010833.1|WP_075268492.1|4701445_4702546_-|transcriptional-regulator
MSDTPARLLKLLSLLQTPREWPGGELAERLDVSPRTIRRDVDRLRDLGYPVEASRGSVGGYRLVAGAAMPPLLLDDEEAVAIAVGLRAGAGHAIEGVDEASVRALAKLEQVLPSRLRHRVSVLQNATVPLTRGDGSTIDPRTLTTLASAATGRERLRFAYRSGDGTRTKRQVEPYRLVSTGQRWYLVAYDIGREDWRTFRVDRVGEPYATGARFTPRPLPVEGAGSDAGGGTGSEGGGGTGSGDAATFLARSMRRMQPELRLDVWFGGPAEFVAARLPAHLGAPEPDGEGGCRLRASCTDSLEWVALRLALVDCEFSVQGPPQLVAYLESLGARLTRAARPADRHRRPGDRHRPACPEQGERGEQG
>NZ_CP010833.1|WP_032766835.1|4700313_4701315_+|sigma-70-family-RNA-polymerase-sigma-factor
MATRAVARRTSAASGETDRASSVRAVGGEIADRDLVGMYLDEIARTPLLDAAKEVDLSQTIEAGVYAQQILDGEVESDAGDAKREELEALVADGERAKDIFIRSNLRLVVAVARRYPRAGLPLLDLIQEGNAGLVRAVEKFDYAKGFKFSTYATWWIRQAITRSIADQSRTIRLPVHLVEELGRIRRVQREFNREHGRDPEHAEIAAELDSNAERVGNVLDWARDPVSLNMSVDDDGDTQFGDLLEDTSAVSPEQSVMTLLRSEELEDLIGKLDNRTASIIKMRYGIEDGRERTLTEVGKQHGLTRERIRQIEKHALLELKRMAHDTGFDAAA
>NZ_CP010833.1|WP_075268491.1|4698814_4699840_-|DUF4243-domain-containing-protein
MDDTTGTLDEALERIHLSGPERDGWLSNHAPMAVEALVRHGQASAVHRWLDRYGPKLEEMPDGTGSPVTARNWREALGDPRRIADWTGYFDRETAERPWRDVLVEWWPRLLPGIAAGATHAVIRVGHSVRTLLAGEETAPRVRELAHALGYWAARHQPLSVPALLGPAPSAAAALDRVPLVPEQSGGIRDRFAQLTAFPEWPAREAASAEAARSALRELVRASTHRYATHAHGEPIMLVHAATAPNAVLRTLPALPGELWEPSLRASWAASAAVTAAYAPREAAPAPASATGAADAGELFARAAAHGDDHTIKFTDTALDVGDALAFSAARRAIELNPPVF
>NZ_CP010833.1|WP_075265810.1|4697947_4698730_+|dioxygenase
MTATAERMPALYLSHGAPPLADDPVWPGELAAWSAGLPRPRAILMVSAHWEEAPLALGATETVPLVYDFWGFPEHYYGVRYEAPGAPGLADSVRKLLRGAGTPVQDIPDRGLDHGAYVPLVEMFPDAGIPVLQISLPTLDPRKLMDVGRKLAPLRDEGVLIVGSGFFTHNLAALRHQGGGVPGWSAEFDDWGDRALRAQDIDALIDFEHTSPAGKLAHPRTEHFAPLFVTLGAAEDELDRGRSVIDGFWMGLAKRSVQFG
>NZ_CP010833.1|WP_075265809.1|4697167_4697680_-|MarR-family-transcriptional-regulator
MESMTTASTSAPRWLSDEEQRVWRAYLHATTLLEDHFDRQLQRDAGMPHIYYGLLVQLSQAPRRRMRMTELARNAKITRSRLSHAIARLEKNGWVRREDCPSDKRGQNAVLTDDGLDMLRRSAPGHVEAVRQAMFDRLTDEQVRSLGEIMRTLATGLEPEGADADLPWLR
>NZ_CP010833.1|WP_075268490.1|4695592_4697125_+|MFS-transporter
MSRTADTALPDPSRWRALAFIALAQLMVVLDATIVNIALPSAQTDLGISDGNKQWVITAYALAFGGLLLFGGRIADLWGRKRTFVVGLIGFALASALGGAAQNEAMMFGSRALQGVFGALLAPAALSLLAVMFTDAKERAKAFGIYGAIAGGGGAVGLILGGFLTEYLNWRWTFFVNIPFAVVAAVGAYFVIREPSGTRNRAPLDIPGVVLSTLGLVALVYGFTRAESAGWSDSLTVSMFIAAAVLLLAFVVTEARVKSPLLPLRVLTERNRGGVYLSLGLAIIAMFGLFLFLTYYLQVVKGYSPVKTGFAFLPMIAGMITGSTQIGTRLMTRVPPRLLMGPGFLVAAVGMLLLTQLDLNTSYAAVILPGMLLLGLGMGTAFMPAMSLATHGIEPRDAGVASAMVNTSQQVGGAIGTALLNTIAASATTAYVADHAARATDPKLLELQAMVSGFAAAIWWAVGILVAAAVIAIALINTGRPGTGQGGTESASGEGAEGAEDEFRIPVVAH
>NZ_CP010833.1|WP_075265808.1|4694656_4695367_+|TetR/AcrR-family-transcriptional-regulator
MKSVAKAVAQAVTGSAAQAVAGKGAAPAGSCRVARPRADALRNRERIVSAARELFVESGPDVPLDDVARRAGVGNATLYRNFPDRAALTHEVVLAVTSRTTLRAEEAVAAESDPFAALSRFVHAAADERIGALCPMISGVFDKDHPDLLAERDRLEEAVAGLVSRAQSAGRLRTDIAVGDVLVALSQLTRPLPGIACQGIDRFTHRHLQLFLDGLETPARSELPGSAATLEDLRRP
>NZ_CP010833.1|WP_075265813.1|4706822_4707932_+|MFS-transporter
MTEPSEATAAAEPPAPGEPAATPPAPTGPRSVTTRATLAGVVVSALLILAIVLGSRMLRNFDSALLPYAVATVFLAFGVAYRYTVWISAPGARRLFKQGWRSLFSVENFRRAPTALPRMIATYLGFQKFLGARSHARWAAHQLIFWGCVLAALITFPLTWGWFTFTSSTGSGPGYEMRIWGFKILGFDSLNLLGWLMFHGLDIAAVLVIPGASYFLWRRMKDRGAITGQRFAYDLVPLIALIVISVTGLLLTFSSVFLHGGGYQFLAILHMVSVVFTLIYIPFGKFFHIVQRPAAVGMQLFKYTGRKDDEVFACRRCEEPIDTGPYVENLRGTMRDLSLDFDAWAEYCPRCKRVLRGSAYLSHVKKGFK
>NZ_CP010833.1|WP_075265814.1|4707928_4710256_+|molybdopterin-oxidoreductase-family-protein
MTADPRAAADRRTFIPLDPSLAPPGTRAFRDAGGIPADRWHADQNGETLVPTHCCFCGVQCGMYLRVDHGGKVFGVEPRNHDINRMRLCPKGINAYQQVNHPDRLTAPLMRRSRDEEFREVSWGEALDFTVSEIKRIQQTYGNDAFGLLGGASLFSEKTYLVGKFARVALKSRHVDYNGRLCMVSAAGANKLAFGIDRAGNPFSDILLTDCLLIAGSNVGECFPVMTQYVWGARDRGATLIVVDPRETAIARTADIHVALKPGTDSAFFTSVLNVVIEEGLTDENFLADHATGWEELKAKAAEYPPSRAAAICGIPAEQIVQVARAFARAPKAMAWHARGIEHHSQGVENCLSVINLCAATGHIGKPGAGYGTITGQGNGQGGREHGQKSDLLPGGRSIMNEEHRRQICEIWGIEESELPPAGTSMMEMVWQMQRREIRGLIGICNNPFVSLPNYRVVKEGYDTTEFHAQFDFFLSETAANAHVVFPVTTWAEDEGVMANAEARVVKHNKAQDPPPGVRTDTWVICELARRLGAGDKFDFPDSRSVFDELRVASAGTVNDYYGITYERLEETGGIAWPCPATDHPGTPRLFEDGKTYHPDGRIHLQVVEWHPPMDPYDDEHPMSLTTGRTVAHFLSGNQTRRLGALVEQTPRPWAEIHPSHGFRNGEPVRIVTRRGSEVFPALVTEAIRPDTVFVPYHWPVPTAANALTIDALDPRSKIPEYKVCACRIEHAERIDEVPAPPVAPGHVAYPETQVSRTDPLPPTAPQGRGTSERS
>NZ_CP010833.1|WP_010059620.1|4710261_4710864_+|4Fe-4S-binding-protein
MMGRTIFIDPGRCIGCQACVSACRECDSHRGKSMIHLDYTDEGQSVASLPTVCMHCEDPVAPCAEVCPADAILVTADGVVQQADTTRCIGCSNCVNACPFGVPKIDLQAKLQMKCNLCYDRTAYGLAPMCATVCPTGALFYGTVEELQAERPGVQVADTFVFGETEVRTGVAMVVPAERVQWPVPGGLPVVEINGKDVRR
>NZ_CP010833.1|WP_075265815.1|4710860_4711634_+|Rieske-(2Fe-2S)-protein
MSVTDQQPGGEHPAGGDPREALQDRIAADSLTTRRDYLRIVTTVSGGLAVGGIGVAAGILHRHGDGEDGKAPEPKRIAGGLLPGESIAFRYPGEEDRAVAVRLDDGTLVGYSAVCTHLACAVLWRKDRGTEGELYCPCHEGVFDARSGEVTAGPPPRGLPKVVVVEQDDGSVWAVGTTRSGESIEEGLCRQLGGERPDLAARIGCPGIDGGAESPPRAAGPRTRNRTTGERPAPRAGGAPQATGVTSATVENPGGRA
>NZ_CP010833.1|WP_075265816.1|4711630_4712026_+|hypothetical-protein
MSDTPHPEQPLPPPGSHYPAYHPGSADPELNRPVHERYPQIRPTSGYGDPRVRHTGPGPGAGTDQNPERSSKLTARLTLAMSVVIGQLWGLTILIDEWMEGNTGTAWWGAGFLCLSFLVVLGLWLVDPKDR
>NZ_CP010833.1|WP_075265817.1|4712087_4712309_+|hypothetical-protein
MSAAPAPSPRDAKQQPQEQPHREPKPKPVLVFDDPLDRQSADDTDQGWGERPPAGNSAADLARFLDEKPPHHI
>NZ_CP010833.1|WP_075265818.1|4712325_4712859_-|large-conductance-mechanosensitive-channel-protein-MscL
MSEKKVSLLEGFKAFLMRGNVIDLAVAVVIGAAFTNIVNAVVKGIINPLVGAFGTQDLDNYSSCLQGPCTTDPKTGQMDGIEILWGSVLSATLSFLITAAVVYFLMVLPMAKYLARRAAMQAAKEGVQETLEVSELEVLKEIRDALVAQRTGGAPGPSSGSTPGGADGTAAGPREDR
>NZ_CP010833.1|WP_075265819.1|4712972_4713491_-|hypothetical-protein
MSTSSSPLSCTAPVPAPSRVGPFGPLRVRGGGADRLRRMLRRQRRAAAAGLALAGAALATTGLSSADGGAGPPDDPPGAGRAPVRLVSAPVRIADPETVRLLRPGDRVDVIAVGDAGDDARVVARGARVAKVPPASTGTGALVVLSVERPTATALLGAGTSGRLAVAVSDAN
>NZ_CP010833.1|WP_075268494.1|4713717_4714536_-|S-methyl-5'-thioadenosine-phosphorylase
MGVIGGSGFYSFLEDVTEVAVDTPYGKPSDSVFLGELAGRRVAFLPRHGRGHHLPPHRINYRANLWALRSVGVRQVLGPCAVGGLRPEFGPGTLLVPDQLVDRTKTRVQTYYDGETRADGTVPNVVHLGFADPYCPEGRKAALAAARGRDWEPVDGGTLVVVEGPRFSTRAESRWHAAMGWSVVGMTGHPEAVLARELGLCYTTMTLVTDLDAGAEAGEGVSHEEVLQVFAANVDRLRSVLFDAVAGLPTSESRNCTCAHALDGIDTGITLP
>NZ_CP010833.1|WP_032766860.1|4714743_4715085_-|FmdB-family-transcriptional-regulator
MPTYQYQCTECGEGLEAVQKFTDDALTVCPSCDGRLKKVFSAVGIVFKGSGFYRNDSRGSSSSSTPASSSSKSSDSGSSSSSTGSDTKSSASSSASSSSAPAPASSSSGTSAA

Crispr_ID: NZ_CP010833_15

• CRISPR_ID: NZ_CP010833_15
• CRISPR_location: 4743746-4743848
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_15

Consensus_repeat	Method
CGTCACCGTCGTCTACGAGCGGTAG	CRISPRCasFinder

spacers of NZ_CP010833_15

>15.1|4743771|53|NZ_CP010833|CRISPRCasFinder
CCCGCGCTTCCGGTCGTCACCGTCGTCTACGGGCGGTAGGCCGCGCTTCCGTT

CRISPR arrays and Neighbor proteins around NZ_CP010833_15

CRISPR arrays

The CRISPR arrays of NZ_CP010833_15

>merge|NZ_CP010833|15|4743746-4743848|CRISPRCasFinder
CGTCACCGTCGTCTACGAGCGGTAGCCCGCGCTTCCGGTCGTCACCGTCGTCTACGGGCGGTAGGCCGCGCTTCCGTTCGTCACCGTCGTCTACGGGCGGTAG

>NZ_CP010833|15|14|4743746-4743848|CRISPRCasFinder
CGTCACCGTCGTCTACGAGCGGTAG	CCCGCGCTTCCGGTCGTCACCGTCGTCTACGGGCGGTAGGCCGCGCTTCCGTT
CGTCACCGTCGTCTACGGGCGGTAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075265833.1|4737131_4737458_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265836.1|4740337_4741846_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|349398
NZ_CP010833.1|WP_075265845.1|4754278_4756510_+|MMPL-family-transporter	unknown	unknown	gnl|CDD|225272
NZ_CP010833.1|WP_075265834.1|4737814_4739035_+|S1-family-peptidase	unknown	unknown	gnl|CDD|367281
NZ_CP010833.1|WP_075265842.1|4748720_4749860_-|aromatic-ring-hydroxylating-dioxygenase-subunit-alpha	unknown	unknown	gnl|CDD|226985
NZ_CP010833.1|WP_075268496.1|4741902_4742352_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_CP010833.1|WP_075265840.1|4746269_4747208_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|131480
NZ_CP010833.1|WP_075265839.1|4744671_4746273_+|NAD(P)/FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224983
NZ_CP010833.1|WP_032781691.1|4742415_4742904_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP010833.1|WP_075265829.1|4729941_4730742_+|amidinotransferase	unknown	unknown	gnl|CDD|224747
NZ_CP010833.1|WP_075265841.1|4747204_4748098_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235633
NZ_CP010833.1|WP_075265846.1|4756664_4757126_-|SsgA-family-sporulation/cell-division-regulator	unknown	unknown	gnl|CDD|377399
NZ_CP010833.1|WP_075265844.1|4753584_4754157_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379883
NZ_CP010833.1|WP_075265838.1|4743866_4744508_-|MerR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|133405
NZ_CP010833.1|WP_075265832.1|4733736_4737123_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_010059661.1|4748232_4748427_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075265835.1|4739092_4740196_-|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|197775
NZ_CP010833.1|WP_075265831.1|4732094_4733468_-|triacylglycerol-lipase	unknown	unknown	gnl|CDD|367570
NZ_CP010833.1|WP_075265830.1|4730741_4731980_+|ornithine--oxo-acid-transaminase	unknown	unknown	gnl|CDD|273853
NZ_CP010833.1|WP_075265843.1|4749987_4753401_-|S41-family-peptidase	unknown	unknown	gnl|CDD|227282

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075265836.1|4740337_4741846_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|349398	cd05379, CAP_bacterial, Bacterial CAP (cysteine-rich secretory proteins, antigen 5, and pathogenesis-related 1 proteins) domain proteins. Little is known about bacterial and archaeal members of the CAP (cysteine-rich secretory proteins, antigen 5, and pathogenesis-related 1 proteins) domain family. The wider family of CAP domain containing proteins includes plant pathogenesis-related protein 1 (PR-1), cysteine-rich secretory proteins (CRISPs), and allergen 5 from vespid venom, among others. Studies of eukaryotic proteins show that CAP domains have several functions, including the binding of cholesterol, lipids and heparan sulfate. This group includes Borrelia burgdorferi outer surface protein BB0689, which does not bind to cholesterol, lipids, or heparan sulfate, and whose function is unknown.	1.20603e-34
NZ_CP010833.1|WP_075265845.1|4754278_4756510_+|MMPL-family-transporter	gnl|CDD|225272	COG2409, COG2409, Predicted drug exporters of the RND superfamily [General function prediction only].	3.66918e-119
NZ_CP010833.1|WP_075265834.1|4737814_4739035_+|S1-family-peptidase	gnl|CDD|367281	pfam02983, Pro_Al_protease, Alpha-lytic protease prodomain.	4.51772e-08
NZ_CP010833.1|WP_075265842.1|4748720_4749860_-|aromatic-ring-hydroxylating-dioxygenase-subunit-alpha	gnl|CDD|226985	COG4638, HcaE, Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit [Inorganic ion transport and metabolism / General function prediction only].	1.40669e-37
NZ_CP010833.1|WP_075268496.1|4741902_4742352_+|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.44347e-16
NZ_CP010833.1|WP_075265840.1|4746269_4747208_+|alpha/beta-fold-hydrolase	gnl|CDD|131480	TIGR02427, b-ketoadipate_enol-lactone_hydrolase, 3-oxoadipate enol-lactonase. Members of this family are 3-oxoadipate enol-lactonase. Note that the substrate is known as 3-oxoadipate enol-lactone, 2-oxo-2,3-dihydrofuran-5-acetate, 4,5-Dihydro-5-oxofuran-2-acetate, and 5-oxo-4,5-dihydrofuran-2-acetate. The enzyme the catalyzes the fourth step in the protocatechuate degradation to beta-ketoadipate and then to succinyl-CoA and acetyl-CoA. 4-hydroxybenzoate, 3-hydroxybenzoate, and vanillate all can be converted in one step to protocatechuate. This enzyme also acts in catechol degradation. In genomes that catabolize both catechol and protocatechuate, two forms of this enzyme may be found. All members of the seed alignment for this model were chosen from within protocatechuate degradation operons of at least three genes of the pathway, from genomes with the complete pathway through beta-ketoadipate. [Energy metabolism, Other].	1.55405e-29
NZ_CP010833.1|WP_075265839.1|4744671_4746273_+|NAD(P)/FAD-dependent-oxidoreductase	gnl|CDD|224983	COG2072, TrkA, Predicted flavoprotein involved in K+ transport [Inorganic ion transport and metabolism].	5.44249e-104
NZ_CP010833.1|WP_032781691.1|4742415_4742904_-|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	2.25885e-13
NZ_CP010833.1|WP_075265829.1|4729941_4730742_+|amidinotransferase	gnl|CDD|224747	COG1834, COG1834, N-Dimethylarginine dimethylaminohydrolase [Amino acid transport and metabolism].	2.56721e-58
NZ_CP010833.1|WP_075265841.1|4747204_4748098_+|SDR-family-oxidoreductase	gnl|CDD|235633	PRK05872, PRK05872, short chain dehydrogenase; Provisional.	4.09309e-145
NZ_CP010833.1|WP_075265846.1|4756664_4757126_-|SsgA-family-sporulation/cell-division-regulator	gnl|CDD|377399	pfam04686, SsgA, Streptomyces sporulation and cell division protein, SsgA. The precise function of SsgA is unknown. It has been found to be essential for spore formation, and to stimulate cell division.	4.92278e-22
NZ_CP010833.1|WP_075265844.1|4753584_4754157_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	6.66982e-21
NZ_CP010833.1|WP_075265838.1|4743866_4744508_-|MerR-family-transcriptional-regulator	gnl|CDD|133405	cd04778, HTH_MerR-like_sg2, Helix-Turn-Helix DNA binding domain of putative transcription regulators from the MerR superfamily. Putative helix-turn-helix (HTH) MerR-like transcription regulators (subgroup 2). Based on sequence similarity, these proteins are predicted to function as transcription regulators that mediate responses to stress in eubacteria. They belong to the MerR superfamily of transcription regulators that promote transcription of various stress regulons by reconfiguring the operator sequence located between the -35 and -10 promoter elements. A typical MerR regulator is comprised of two distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	2.00054e-58
NZ_CP010833.1|WP_075265843.1|4749987_4753401_-|S41-family-peptidase	gnl|CDD|227282	COG4946, COG4946, Uncharacterized protein related to the periplasmic component of the Tol biopolymer transport system [Function unknown].	1.31404e-92
NZ_CP010833.1|WP_075265835.1|4739092_4740196_-|helix-turn-helix-transcriptional-regulator	gnl|CDD|197775	smart00530, HTH_XRE, Helix-turn-helix XRE-family like proteins.	0.000150869
NZ_CP010833.1|WP_075265831.1|4732094_4733468_-|triacylglycerol-lipase	gnl|CDD|367570	pfam03583, LIP, Secretory lipase. These lipases are expressed and secreted during the infection cycle of these pathogens. In particular, C. albicans has a large number of different lipases, possibly reflecting broad lipolytic activity, which may contribute to the persistence and virulence of C. albicans in human tissue.	1.58532e-35
NZ_CP010833.1|WP_075265830.1|4730741_4731980_+|ornithine--oxo-acid-transaminase	gnl|CDD|273853	TIGR01885, Ornithine_aminotransferase, ornithine aminotransferase. This model describes the final step in the biosynthesis of ornithine from glutamate via the non-acetylated pathway. Ornithine amino transferase takes L-glutamate 5-semialdehyde and makes it into ornithine, which is used in the urea cycle, as well as in the biosynthesis of arginine. This model includes low-GC bacteria and eukaryotic species. The genes from two species are annotated as putative acetylornithine aminotransferases - one from Porphyromonas gingivalis (OMNI|PG1271), and the other from Staphylococcus aureus (OMNI|SA0170). After homology searching using BLAST it was determined that these two sequences were most closely related to ornithine aminotransferases. This model's seed includes one characterized hit, from Bacillus subtilis (SP|P38021).	5.22598e-180

Protein sequences

>NZ_CP010833.1|WP_032781691.1|4742415_4742904_-|GNAT-family-N-acetyltransferase
MLIHPRPFDHPDAVKLNDQVQLEYAERYGDEGDVTPLDPSMFVPPHGLYLLAYDEQERPVATGGWRTQNLNAEGYEDGDAEIKRMFVIPEGRGRGLARRMLAALEEDARAAGRTRMVLETGDQQPEAVALYTSCGYTVCDVKFGHYRTYDSSICMAKPLRQP
>NZ_CP010833.1|WP_075268496.1|4741902_4742352_+|GNAT-family-N-acetyltransferase
MQLRDVVPEDLEVFLAYEHDPEAVRRSRFAPRERDAFMAHWRTRVLGDPANFVQTVVVDGETAGNIVAWWEEDRRFIGYWFGRAYWGRGIGTGALTAFLERETARPLYADPAASNTGSVRLLEKCGFTATGTVRHGEDEHVMLVLGGGA
>NZ_CP010833.1|WP_075265836.1|4740337_4741846_+|sigma-70-family-RNA-polymerase-sigma-factor
MNGVDSTTLVIAARNGDRAAGERLAAQYLPLVYNVVGRALNGHPDVDDVVQETMLRALSGLPALRDPARFRSWLVAIAMNQVRSRWSNLGHRPAPLEETSEPADPAADFVDLTILRLELSGQRRETAEATRWLDEGERDVLSLWWLETAGDLTRSELAEALGLSPQHAAVRVQRVKNQLDVGRTVVRALASDPRCPALEDLLGDWDGTPTPLWRKRIARHVRGCASCSDGSAGLVPPEGLLSGLALVVPLYDSGQQVAAAVASSAAPATAAAPSAAAHAAPAAFSAGKAAGLIAGAAAVTALAVLIWPSAPAEPESRGGGVTAGPAPAPPPASASAEPSPSPSTVPPTPTPSRTAATRPPTVSPSPSASPAPKPRPGPDARVVTRVNTLRAANGCPELETDPRLTEVAQRHSEDMAARNYFDHTDSSGRGPGDRVGATGYAWSAVGETIATGMSDPAAVVEEWRNSPGRDDDIFNCDFVHVGVGIADSPRGPYWTQVLATPS
>NZ_CP010833.1|WP_075265835.1|4739092_4740196_-|helix-turn-helix-transcriptional-regulator
MSSDTQTDEAHATGPGSTGAQDTDPRATEAHATPAQHAEAHATAARTGEALTTSALHAAATGADTFPGVLREALNRRGLSLERVSERLRVRGITISQATLSSWQRGRSQPERARSLQAVDVLEEILELPAGSLRSLLGPRRPRGRTTPPDAEGAALQILGEDSVVEKALGARFRHFNQETSSLMVHDIVRVGETGTLSGISTTNVLRAKRAGADRAIFVLSFDDEAAEPVDIRVTCGRLAEATYLKGLKSLVLEIHFGRELAKLDTTVVSYAVEVSPSDTPATHYERWSRTNLHEYLQQVFFHPGALPADCHRYVREKVGDPPRGRRRIPLSEAHDVHVLTSRCKPGVHGVAWEYGTGRSGTGDRPG
>NZ_CP010833.1|WP_075265834.1|4737814_4739035_+|S1-family-peptidase
MKHGKKNARRYIVAASIGALLSAGVATGAYAGTTEEPSAPASAPAYQPDMVKALAVTLGVSEKAAVERLDREADQQDRFAELRKDRVDTLGAFFTKDGSLVVNAADAEAAKDVRAAGLKARVPERGESELDRIKAQLDAKALKSAPAGVSAWSVDLASDTVTVEVNGDTDAATRSFLKAAQSNGEAVRVVKGQEKLETQAVVPPGSRMTFNGYLCSVGYGAKDRNGKQVLVTAGHCIEDLPELAYNGTRFAKGTHTRFALGTRSVDMGIASVDAGNSIGLDITTYGKAGTVPVKGSKRAPSGAALCKSGQTTNWTCGKVGSYNVSVTYTDQNGGPDTVVTGLASSSVCTQGGDSGGAYVSGDQAQGMTSGGPSNQRCNGQVNSPGSSYFQPLDDALAYYGLTLNTK
>NZ_CP010833.1|WP_075265833.1|4737131_4737458_-|hypothetical-protein
MWTGLAVAVLAGVLSFLSWDRADQMAGVVSAVVGVAALGVGVYGALGPARGPDVQVSGTGRAVSRGGGEANTGFVSPAPTTAPGSVSVSDTGDAEADGGGANTGFRQG
>NZ_CP010833.1|WP_075265832.1|4733736_4737123_-|hypothetical-protein
MTGGRIGAKDTGDASAQGDVAFSNTGVFNGSVTLARQRPAVSGYLLQVERVAAADFRGREAELSELASFGTEERPQGAAERNYWRWLAPAWAGKSALLAEFVLNPPPGIDVVAFFITSRMAGQNDATAFCEVVQRQLYALLREEEPLSTPATRDEQLRLAMDRAAERCAAEGRRLVLVVDGLDEDHGVTAGPDCHSIAALLPRTPPHGMRIIVAGRPHPPVPDDVPGDHPLRTAQINHWLAPSPYAQAVRWDAEQNLLRLLDGGGLGRELVGLTVAAGGGLSARDIAELTGSRPRLVERELSAVTGRSFRRRSVHWASHGPEVYLLAHEEIQRSAAELITDAELADFRTRLHRWAQTYRSAGWPATTPEYLLRGYAQLLRELGSTGQLVELVCDAARHERLWQVTGADLEALSELSTSLDQLLAHGRQSGDLDVSAALRLAAARDGLHKRTAVLPAGLIGLWARLGHTGRAISLAESQQKSYNRVSALTSVATCLAATGHRERAEALAADADSGEDEARFLEAVAEGLAEAGLYSEAFRTTARTEGTDRLAKALVATVRRAAGDHASHGRVGKKAITPHLAEAVQAVATVRGVEQGELYADLACAFSLFGDEEQARETIDLAVRDRSDGEGAFRQAQNLSHVAERLAPAPGLAQRAASIARDAAELAGTIDDPRSVEWLFPQIAAGLAATGQYERAEQVAGVLPDPADFDEGLCAAARAAAEAGAPGWALEVADRLTDPIDRASVLVAVGRRAARSADPAETSQLARRVLTVIEEVSPEVWRVGLLTSTSEFLLLAGAREQAEAVATTATVLARNRTTPRGSVTAQIAVARALAAAGAEAEAHRLVDWAMESAEAEDGYVRLLRLVDVAGGLHAIGQDDRKVAMLSALLDEAREEAHHSEHAESQQHVAEAFGETGHPDLARKVARELLASADALDSAYQQGWNRYSAAGAYLAAGDFDKALALTDSLPDDVVADFRSGVVEKLVAAGEYAWAGRLAWELTGTVEGDRSLIHIAAGMAARGDVPGAVALLDEISVPGLRDEAMREIVSASPRADAPHEAHSLADAITDPVHRSKALAAIARAHGPTPKGRVLLVEALALGPWNELVEEIAGVAPEHLLLLAALSRNEH
>NZ_CP010833.1|WP_075265831.1|4732094_4733468_-|triacylglycerol-lipase
MNRSTAGLLAVAVVTALTAGAAPTAWATPTAGTPATATPAAAAQTGSKASDPFYRYDGSEPLSSYAPGDVLKKRTLDYHVLGIPTPVKAVQLLYRTTDAQGRPSANVTTVVRSHRGDGSKAVSYQSFYDSLDPEDGPSRAIAGKVTLGGIIANVESIVMAPLLLKGYDLVIPDTEGQTAEFAAGPAYGTNTLDSIRASTRAAGTGLHGGTRFGLLGYSGGAIATNWAAALAPAYAPEVNQQLVGFAGAGLLVAPAHNLKYVDGSLVWNGVIPMAVIGVSRAYGIDIRRYLNPKGVAVFDELEHGSIVDALGRYPGMTWKDLAKPEYKDPNSIPAFVDAVNKVNLGEAATPTVPGFIGQGNAGVLEGTFNRPPGIGTGDGVMVAGDVRALANQYCATGNKSIKYEQYDLLSHFGAMPYWTPRAMSWLDDRFAGKAAPTSCGRIPAGNSLAPEKPAVTN
>NZ_CP010833.1|WP_075265830.1|4730741_4731980_+|ornithine--oxo-acid-transaminase
MTDTVTPPSAAPETRSSEQLIRAEAPVLAHNYHPLPVVVARAEGTWVEDVEGRRYLDLLAGYSALNFGHRHPALIEAAHRQLDELTLTSRAFHHDRLAGFAERLAALTGLDMVLPMNTGAEAVESAVKVARKWAYEVKGVAPDRATIVVADGNFHGRTTTIVSFSTDGTARAGFGPFTPGFRVVPYNDLAALESALDETTAAVLIEPVQGEAGVVIPDDGYLTGVRELTRRAGCLFIADEIQSGLGRTGRTLAVDHEGVVPDMLLLGKALGGGIVPVSAVIARREVLSVLGPGEHGSTFGGNPLSAAIGSAVLDLLATGEFQRRAAELGEVLDRGLAALVGAGVTGYRARGLWAGVDIDPAIGTGREISERLLAEGVLVKDTHGSTVRLAPPLTITEEELGSALTALAKVLA
>NZ_CP010833.1|WP_075265829.1|4729941_4730742_+|amidinotransferase
MCEPRYFEVAYAINPWMDTGTPVDLPLARDQWLTLVEAYRDHGHTVETIDPVAGLPDMVFAANAALVMDGKVFGSSFHAPERQPEAAAYAQWFKEAGYEVHPSRSVCEGEGDLVPAGRYVLAGTGFRTHSSAHREAQEFFGRPVIGLDLVDPRFYHLDTALFDLGGAPDGGDGTDAGNIAYYPAAFSAGSREVLRHLYPDAVIATEEDALAFGLNSLSDGRHVFVAPQAQGLIDDLAHRGYVPVPVGLSEFHKAGGGIKCCTQEIR
>NZ_CP010833.1|WP_075265838.1|4743866_4744508_-|MerR-family-transcriptional-regulator
MEELAKEAGITVRTLRFYRERGLIPPPRREGRIAWYDAHHLARLRTIAGLLERGHTLNGIADLAATFESGRDVAEVLGLGEPTEETPVRLTPEQLADYFEGEVTPENLAAALDLGYLATDGDEIVHISRRLLEVSAELVREGVPLATVLSSGRRVREHAEALAEIFVRVLHAHAKETEPAQLRPLARAVVDAELSMALDRRLRREDGTQPPKA
>NZ_CP010833.1|WP_075265839.1|4744671_4746273_+|NAD(P)/FAD-dependent-oxidoreductase
MAQQEHVRVAVIGTGFGGLGAAVRLRREGITDFVVLERAGSVGGTWRDNSYPGCACDVPSHLYSFSFAPNPDWPRTFSGQEHIRAYLERVADTFGLRPHIRLNHEVKLMSWDKENLYWVIESANGTTLHADVVISATGPLSDPKMPDIPGLDSFPGKVFHSARWDHDYDLAGKRVAMVGTGASAIQIVPAIQPKTAKLTLFQRTPPWVMPRMDRTISKAERALHRAIPATGTARRGLLWGIRELQVSAFTKHPDQLGLVETIAKSNMARAIKDPALRAKLTPDYRIGCKRILLSSTYYPALAQPNVDVVASGLSEIRGSTVIAADGTEAEVDAIVFGTGFHVTDMPIAERVVGAEGITLAETWKDGMNSLRGATASGFPNWMTIIGPNTGLGNSSMILMIESQLNYMADYLRQLNVLGGRAALDARSGSVTAWNDKVQQRMKRTVWNTGGCTSWYLDEAGRNTTVWPGTTGEFRRQTRSVDLAEYDVVRAGGAGGDRRAAGVGRVPEQPGRTDRETVTAAAAEAGPVAEEATR
>NZ_CP010833.1|WP_075265840.1|4746269_4747208_+|alpha/beta-fold-hydrolase
MSRLLHRDTVPPVPAAELTARSADGARIHVELHGPEDAPAVVLAHGWTCNTRFWDAQIRELAADHRVIAYDQRGHGLTPEPGPGGYSTNALADDLEAVLAATLAPGQKAVLAGHSMGGMTVMAAASRPGVREHAAAVLLCSTGATRLAAEALVLPLRAGALRTRLTTAVLGAKAPLGPVNPVSRKILKYATMGRGSAPDRVDACARIVHACPRRARVEWGHVLGELDLAEGVRALRVPTAVIAGTDDRLTPPVHARAIVDALPVGLGLTELTGMGHMTPVEAPEAVSAKIRELVTRYVATGAAATAEKEDVA
>NZ_CP010833.1|WP_075265841.1|4747204_4748098_+|SDR-family-oxidoreductase
MSGKRNLEGQVVVVTGAARGVGELLARKLSARGATLALVGLEPDELKQVSERLHGESDHWFADVTDHEAMAQVAREVKERFGKVDVVVANAGVAAGGPFADSDPAAWRRVIEVNLIGGAVTGRAFLPVLTESRGYFLQIASLAAITPAPMMTAYCASKSGVEAFAHSLRAEVGYKGVKVGVGYLSWTDTDMVRGADQDDVMRELRQRLPWPMNRTYPLGPAVDRIVDGIARRSPHVYAQWWLRGMQSVRGYLPSVIALGGQREMRRFEPRLHTVSKGLVGAGGAADHDARAERADRS
>NZ_CP010833.1|WP_010059661.1|4748232_4748427_+|hypothetical-protein
MGIADQFKDKAQELADQAKQKAGQGKDQAKERGQQARDQRSDSSSGMQDRAQDAADQARERFDR
>NZ_CP010833.1|WP_075265842.1|4748720_4749860_-|aromatic-ring-hydroxylating-dioxygenase-subunit-alpha
MTENRSDQIARGRPGEGPGPAPAPPDLRRIGADPDFWYPVALSRNVRKEGVAAAVFAGERIALYRAKSGAVHALEDRCAHRQVPLSMGVVDGETLRCCYHAWAYRGDGRISQIPYLAKGDARPPRGVRAYPVREAYGLVFVFPGDPEKAEVTPLPDVPAYASPRYRTMTFSRTVRCHYSFLHENLLDMNHQFLHRGVVGKLQPKLLGYESGPASVEARYLFTHTGGKRNRSASLLAAEGLGGQPSSDVMTIRTEYPYQTLDLVPEKADHPALRLWAVYVPEDAEQRVCHAYGLLMIEKPRIPAALSVAWPFIRHFTERVFAEDRMAVEAEQRAWDEQGEDRNHEVFSLILDVRDVLRANGVPLSPRTTADTRSCEGLAP
>NZ_CP010833.1|WP_075265843.1|4749987_4753401_-|S41-family-peptidase
MSDDVAYLRFPHLHQDLLCFAAEDDLWVAPLAAAGHRPGRAWRVTVDRTRVSHPRFSPDGTSIAYTTWRTLDPEIHLAPVDGGPARRLTYWGSTDARVCGWSPDPGDACQILAVSSHNQPFSYFSWAYSVPTDGSPGGRLPWGPVSDIAVADIDGERRTLLLTGTPPHEPAAWKRYRGGAMGRLWLHGERLLPDIDGHLANPMFVGRRIAFLSDHQGVGNLYSCRTDGTDLRRHTDHDAFYARNASSDGHRVIYQCAGELWLVEDLESPDATPRKLEVRLGGPRTGRRVHQVPAASNVDSLSVDETGRASAVTVRGSLYWLTHRDGPARTIADTPGVRVRLPEMLGSGGQVAYVTDADGPDAVEIAYLPRASGDRPPRRLATGQLGRVQEMISDPDGKRLAIASNDGRLLLLDTGEEEAEVEAPEPVEPVEPVVKAPSGSTRADLHAATGAATPDSAVPVDEHPGLTELIRSVNGPVRDLAFSPDGDWLTWSHPGVGRSLRQIKLARISGPGAPVIVDVTNGRFEDENPVFTEDGRYLAFLSWRGFDPVYDVHTGDLSFPLGCRPYLVPLSSATPSPFALSPDGRPAAGGLDPVDVPEGGGTSEGSTVMVEFEGLESRVTPFPVSASKYSALAPVSGGGLVWLRWPISGALGETFANPADMSGRPTLEHFNIAKARRTELVDHLDWFAVSGDSSRLVVMDDGELRAVPATEPGDGDTTVYLDLRRILHEVDPGAEWRQAYGEAGRIIRDYFWEPDMCGIDWDGVLDQYRPLVERVASPDEFADLLREVLGELGTSHAYVSPARRNEGPPHYQRAIGLLGANLVCRDGAWTIQRILPGDSSDSKARSPLAGTGIREGAVLTHVDGRPVDPVAGPYPLLTAAGGTTVELTFTPAGGGPSRRVAIMPLVDERPLRYQDWVAKRRDVVRELSGGKCGYLHIPDLGGSGWAQFNRDLRLEVARPALIVDVRGNAGGHISELVVEKLTRTILGWDLTRNAQAVSYASNAPRGPVVALADEATSSDGDMITAAFRLLKMGPVVGQRTWGGVVGMTGRHRLGDGTSITVPMNAAWFDTYGWSVENHGVEPDVEALRTPLDWAEGRYRVLDDAVGLALDLLAAHPAATPPSYDTAPDLRRPPLPPR
>NZ_CP010833.1|WP_075265844.1|4753584_4754157_+|TetR/AcrR-family-transcriptional-regulator
MARTRLTPEREGELYEAVLDLLREVGYDALTMDAVAARTRSSKATLYRQWGSKPELVAKAMRHNKPGNLSDIDTGSLRGDFHAALSRTDDCQMEKDTALMRGLAHAIHEYPDLLKALRELLIEPEMTGFDQMLQRAVDRGELRADNPALKYIVHMVIGALAARELIEDQPVDQAFLIDYVDSVVLPALGV
>NZ_CP010833.1|WP_075265845.1|4754278_4756510_+|MMPL-family-transporter
MATFLYKLGRLTFRRRGFVALIWVALLAAGILGAATASTATSSSFSIPGTEAQRAFDLLEERNPGGSADGATARVVFQAPEGEKVTDAGNKREITGIVKELQSGSDQIARVADPFQQKAVSQNGSTAYISVSYKVNSMELTDATRDALEDAGKDARKSGMKVEIGGDALQVMPHTGTAEIIGVVIAAIVLVITFGSLIAAGLPLVTALVGVGIGVSTITALASVMDLGSTTSILAMMIGLAVGIDYALFIVSRYRAELAEGREREEAAGRAVGTAGSAVVFAGLTVVIALAGLAVVNIPMLTKMGLAAAGTVAIAVLIALTLVPAALGFAGKRIMGRKARKAAEAEKSPDAKPNMGTRWARFVLRKPVWVMLVGVLGLGIVAVPAASLEMGLPDDGAQPKSTTQRQAYDMLSDGFGPGFNGPLMVVTDTKNSSDGKAAANRVAEEIEALGVSAVLPPAFNKAGDTATITVIPKDRPSSHATEEVVHDIRDAGKDIKADTGAEVLVTGATAMNIDFSQKMNDALLPYLALVVGLAFLLLMLVFRSILVPLKAALGFLLSVVAALGAVVAVFQWGWLGSLFGVEQTGPIMSMMPIFMVGVVFGLAMDYEVFLVTRMREAYVHGESPGQAIVTGFKHGARVVTAAAVIMMAVFSGFIGSSEQMIKMIGFSLAIAVLFDAFVVRMAIVPAVLALLGRKAWWLPRWLDRALPNVDVEGEKLQQQLTDTSDSAGSGDGGGEGERELVRV
>NZ_CP010833.1|WP_075265846.1|4756664_4757126_-|SsgA-family-sporulation/cell-division-regulator
MSPVIEEHARARLITDGPLTRPVPVDLRYDPADERRTVHIGLPDGTDWAFGRDLLERGLRTPIERGAVRVWPCGRTQLIVELHSTDGVEVFQFEIRTLIRFLARTHRTQTPGASPDTGREPQPPSRTTRPDTSRTIRPDQGTEQERGAQPAHG

Crispr_ID: NZ_CP010833_16

• CRISPR_ID: NZ_CP010833_16
• CRISPR_location: 5012710-5012847
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_16

Consensus_repeat	Method
AAGATGCCCTCAATCGCCGGGCGGGCTTGAAGTGGCCGGG	CRISPRCasFinder

spacers of NZ_CP010833_16

>16.1|5012750|58|NZ_CP010833|CRISPRCasFinder
TCAATCGCCGGGCGGGCTTGAAGTGGCCGGGGTTGGGTCGGATGGCGCGCGCCCGGGA

CRISPR arrays and Neighbor proteins around NZ_CP010833_16

CRISPR arrays

The CRISPR arrays of NZ_CP010833_16

>merge|NZ_CP010833|16|5012710-5012847|CRISPRCasFinder
AAGATGCCCTCAATCGCCGGGCGGGCTGGGGAAGATGCCCTCAATCGCCGGGCGGGCTTGAAGTGGCCGGGGTTGGGTCGGATGGCGCGCGCCCGGGAAAGATGCCCTCAAACGCCGGGCGGGCTTGAAGTGGCCGGG

>NZ_CP010833|16|15|5012710-5012847|CRISPRCasFinder
AAGATGCCCTCAATCGCCGGGCGGGCTGGGGAAGATGCCC	TCAATCGCCGGGCGGGCTTGAAGTGGCCGGGGTTGGGTCGGATGGCGCGCGCCCGGGA
AAGATGCCCTCAAACGCCGGGCGGGCTTGAAGTGGCCGGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075266014.1|5004950_5005457_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266015.1|5005519_5006206_+|HAD-family-hydrolase	unknown	unknown	gnl|CDD|223620
NZ_CP010833.1|WP_075266023.1|5020626_5021814_+|CDP-glycerol-glycerophosphotransferase-family-protein	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_075266026.1|5027285_5030150_+|CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_075266021.1|5015487_5016711_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266010.1|4999163_5000351_-|winged-helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|225755
NZ_CP010833.1|WP_075266016.1|5006487_5007117_-|DJ-1/PfpI-family-protein	unknown	unknown	gnl|CDD|153243
NZ_CP010833.1|WP_075268513.1|5022723_5023572_+|methyltransferase	unknown	unknown	gnl|CDD|377550
NZ_CP010833.1|WP_075266018.1|5012856_5013648_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213187
NZ_CP010833.1|WP_075266009.1|4998381_4999137_+|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP010833.1|WP_075266013.1|5004165_5004675_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266025.1|5023791_5027289_+|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_075266011.1|5000416_5001037_-|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_CP010833.1|WP_075266024.1|5021854_5022679_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|369777
NZ_CP010833.1|WP_075266020.1|5014752_5015373_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379883
NZ_CP010833.1|WP_075266017.1|5007571_5012587_+|NAD-glutamate-dehydrogenase	unknown	unknown	gnl|CDD|377452
NZ_CP010833.1|WP_075266022.1|5016799_5020525_-|glycosyltransferase	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_107472816.1|5013640_5014561_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_CP010833.1|WP_075266012.1|5001277_5004097_+|preprotein-translocase-subunit-SecA	unknown	unknown	gnl|CDD|237259
NZ_CP010833.1|WP_006124981.1|4997508_4998198_+|ribosome-associated-translation-inhibitor-RaiA	unknown	unknown	gnl|CDD|238308

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075266015.1|5005519_5006206_+|HAD-family-hydrolase	gnl|CDD|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	2.24323e-25
NZ_CP010833.1|WP_075266023.1|5020626_5021814_+|CDP-glycerol-glycerophosphotransferase-family-protein	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	2.19285e-144
NZ_CP010833.1|WP_075266026.1|5027285_5030150_+|CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	3.29775e-101
NZ_CP010833.1|WP_075268513.1|5022723_5023572_+|methyltransferase	gnl|CDD|377550	pfam05711, TylF, Macrocin-O-methyltransferase (TylF). This family consists of bacterial macrocin O-methyltransferase (TylF) proteins. TylF is responsible for the methylation of macrocin to produce tylosin. Tylosin is a macrolide antibiotic used in veterinary medicine to treat infections caused by Gram-positive bacteria and as an animal growth promoter in the swine industry. It is produced by several Streptomyces species. As with other macrolides, the antibiotic activity of tylosin is due to the inhibition of protein biosynthesis by a mechanism that involves the binding of tylosin to the ribosome, preventing the formation of the mRNA-aminoacyl-tRNA-ribosome complex. The structure of one representative sequence from this family, NovP, shows it to be an S-adenosyl-l-methionine-dependent O-methyltransferase that catalyzes the penultimate step in the biosynthesis of the aminocoumarin antibiotic novobiocin. Specifically, it methylates at 4-OH of the noviose moiety, and the resultant methoxy group is important for the potency of the mature antibiotic. It is likely that the key structural features of NovP are common to the rest of the family and include: a helical 'lid' region that gates access to the co-substrate binding pocket and an active centre that contains a 3-Asp putative metal binding site. A further conserved Asp probably acts as the general base that initiates the reaction by de-protonating the 4-OH group of the noviose unit.	2.12612e-42
NZ_CP010833.1|WP_075266010.1|4999163_5000351_-|winged-helix-turn-helix-domain-containing-protein	gnl|CDD|225755	COG3214, COG3214, Uncharacterized protein conserved in bacteria [Function unknown].	1.92399e-73
NZ_CP010833.1|WP_075266012.1|5001277_5004097_+|preprotein-translocase-subunit-SecA	gnl|CDD|237259	PRK12904, PRK12904, preprotein translocase subunit SecA; Reviewed.	0
NZ_CP010833.1|WP_075266018.1|5012856_5013648_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	1.1021e-93
NZ_CP010833.1|WP_107472816.1|5013640_5014561_-|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	3.76496e-40
NZ_CP010833.1|WP_075266025.1|5023791_5027289_+|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.73601e-104
NZ_CP010833.1|WP_075266011.1|5000416_5001037_-|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	4.03094e-29
NZ_CP010833.1|WP_075266009.1|4998381_4999137_+|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	3.68694e-78
NZ_CP010833.1|WP_075266024.1|5021854_5022679_+|methyltransferase-domain-containing-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	3.92254e-10
NZ_CP010833.1|WP_075266020.1|5014752_5015373_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	8.71354e-22
NZ_CP010833.1|WP_075266017.1|5007571_5012587_+|NAD-glutamate-dehydrogenase	gnl|CDD|377452	pfam05088, Bac_GDH, Bacterial NAD-glutamate dehydrogenase. This family consists of several bacterial proteins which are closely related to NAD-glutamate dehydrogenase found in Streptomyces clavuligerus. Glutamate dehydrogenases (GDHs) are a broadly distributed group of enzymes that catalyze the reversible oxidative deamination of glutamate to ketoglutarate and ammonia.	0
NZ_CP010833.1|WP_075266022.1|5016799_5020525_-|glycosyltransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.77036e-80
NZ_CP010833.1|WP_075266016.1|5006487_5007117_-|DJ-1/PfpI-family-protein	gnl|CDD|153243	cd03169, GATase1_PfpI_1, Type 1 glutamine amidotransferase (GATase1)-like domain found in a subgroup of proteins similar to PfpI from Pyrococcus furiosus. Type 1 glutamine amidotransferase (GATase1)-like domain found in a subgroup of proteins similar to PfpI from Pyrococcus furiosus. PfpI is an ATP-independent intracellular proteases which may hydrolyze small peptides to provide a nutritional source. Only Cys of the catalytic triad typical of GATase1 domains is conserved in this group. This Cys residue is found in the sharp turn between a beta strand and an alpha helix termed the nucleophile elbow.	1.33357e-92
NZ_CP010833.1|WP_006124981.1|4997508_4998198_+|ribosome-associated-translation-inhibitor-RaiA	gnl|CDD|238308	cd00552, RaiA, RaiA ("ribosome-associated inhibitor A", also known as Protein Y (PY), YfiA, and SpotY, is a stress-response protein that binds the ribosomal subunit interface and arrests translation by interfering with aminoacyl-tRNA binding to the ribosomal A site. RaiA is also thought to counteract miscoding at the A site thus reducing translation errors. The RaiA fold structurally resembles the double-stranded RNA-binding domain (dsRBD).	1.93523e-26

Protein sequences

>NZ_CP010833.1|WP_075266017.1|5007571_5012587_+|NAD-glutamate-dehydrogenase
MQTKLDEAKAELLAGAAKVADNGPGGGVGGPGGAPRARASAGGADAGASAGQDTVLAYLQRYYLHTAPEDLSGRDPVDVFGAAASHYRLAENRPQGTANVRVHTPTVEENGWACSHSVVEVVTDDMPFLVDSVTNELSRQDRGIHLVIHPQVTVRRDVAGKLIEVLSGGPGTPKASQGRKKSKDAKGEKSELPHDALVESWIHVEIDRETDRADLQQITADLLRVLSDVRETVEDWGKMRDAALRIADDLPGEPLDDLADEEVEEARELLRWLAADHFTFLGYREYELKDSDALAAVPGTGLGILRSDPQHSEDEAHPVSPSFDRLPADVRAKAREHKLLVLTKANSRATVHRPSYLDYVGVKKFDAKGNVVGERRFLGLFSSAAYTESVRRVPVIRRKVAEVVEGAGFSYNSHDGRDLLQILETYPRDELFQTPVDQLRAVATSVLYLQERRRLRLYLRQDEYGRYYSAIVYLPRDRYTTGVRLRLIDILKEELGGTSVDFTAWNTESILSRLHFVIRVPAGTELPHLTDADADRIEARLVEAARSWADGFGEALTAELGEERAAELNRQYGHSFPEGYKADHSPRAAVSDLVHLETLREGEKDFALSLYEPVGAGPGERRFKIYRTGEQVSLSAVLPALQQLGVEVVDERPYELRCADRTHAWIYDFGLRMPLVNGNGGYLADDARARFQEAFAAVWKGEAENDGFNALVLGAGLNWRQAMVLRAYAKYLRQAGSTFSQDYMESTLRNNVHTTRLLVSLFEARMSPGRQSAGTELTDGLLEELDGALDQVASLDEDRILRSFLTVIKATLRTNFFQHTEDGEPHSYVSMKFDPQAIPDLPAPRPAFEIWVYSPRVEGVHLRFGKVARGGLRWSDRREDFRTEILGLVKAQMVKNTVIVPVGAKGGFVAKQLPDPSVDRDAWFAEGIAAYRTFISALLDITDNMVAGEVVPPTDVVRHDEDDTYLVVAADKGTASFSDIANEVAVAYGFWLGDAFASGGSAGYDHKGMGITARGAWESVKRHFRELGHDTQTEDFTVVGVGDMSGDVFGNGMLLSEHIRLVAAFDHRHIFIDPNPDAATSYAERRRLFDLPRSSWADYDTDLLSAGGGIHPRSAKSIPLNAHIREALGIDASVSKMTPADLMQTILKSPVDLVWNGGIGTYIKAVSESNADVGDKANDAIRVNGEDLRAKVVGEGGNLGATQLGRIEFARNGGRINTDAIDNSAGVDTSDHEVNIKILLNGLVRDGDMTVKQRNKLLADMTDEVGALVLRNNYAQNVALSNASAQAPSLLHAQQRFMRRLERDGALDRALEFLPADRHIRELLSNEKGLSQPELAVLLAYTKITTADELISTVLPDDPHLQKLVHAYFPSALRERFPEAVDGHALRREIITTVLVNDTVNTAGSTFLHRLREETGASIEEIVRAQFTAREIFGLSQVWDAVEALDNKVAADVQTRIRLHSRRLVERGSRWLLGNRPQPVAISETIDLFRDGVEQVWNELPKLVRGADLDWYHSILDELTAAGVPDGLAVRVAGFSSAFPALDIVAIADRTGKEPLEVAEVYYDLADRLRITQLMDRIIELPRADRWQSMARASIREDLYAAHAALTSDVLSVGNGSSTPEERFRAWEEKNAAILARSRSTLEEIQGSDAFDLANLSVAMRTMRTLLRTHA
>NZ_CP010833.1|WP_075266016.1|5006487_5007117_-|DJ-1/PfpI-family-protein
MPQKILIVTGDAAESLEVLYPYQRLLEEGYEVDIAAPERKTLRFVVHDFEPGFDTYTEKPGYTWPADLSFSEVDPGAYIALVIPGGRAPEYLRNNAELRKIVGAFFSADRPVAQICHGPLITAATGHLSGRAVTAYPALEPDMQSAGATFQDTEAVVDGPLVSSRAWPDHAAWMREFLRVLRSSGPGAPSSPSDTLYSPTGTPSSPSGD
>NZ_CP010833.1|WP_075266015.1|5005519_5006206_+|HAD-family-hydrolase
MTSGTTRTHLVWDWNGTLLDDTHAVIRATNAAFAEVELAPITLEQYREMYTIPIPRFYERFLGRLPTEAEWERMDGVFHRYYTEQRAACGLTAGAEELLHEWQRAGRSQSLLSMYGHEQLVPVVRGYGIEPRFVRVEGRTGPSGGSKALHMERHFAALAGAGGVDGFSPESVVVIGDALDDAVAAAHVGARAVLYTGGSHSRSSLEGAGVPVVDSLGEAVALAETFSA
>NZ_CP010833.1|WP_075266014.1|5004950_5005457_+|hypothetical-protein
MRVYVPLTLSGLAAAHGAGEVGPGPLTAYAVTPGLREWYVSDDIEELEYAALNRAAAASLRMIAGSPDEARRRVVVALDVPDGSAVADPDHGLSAASLGEVRIAAALPLAKAAAVHVDADDAEKDVAAAAAALGAADLGDDDAQFTVDGAEDHELLWFGVQEIPQLIR
>NZ_CP010833.1|WP_075266013.1|5004165_5004675_-|hypothetical-protein
MSTDRTRPAGRRDQHGPRSAPSGPRSASNGPRPVPSGPRSVPPQRSRRLQPHRPLRPHQWFAERLLAVLSGQRPVHWMLGHTIGEAYDQLAELAPSTPLRTTHGSRPVLRHCRGAQPATGVVEAFASIAAGDRVRAMAFRLEQGADQRWRCAAVELGGERLTAGAPGPR
>NZ_CP010833.1|WP_075266012.1|5001277_5004097_+|preprotein-translocase-subunit-SecA
MSVFNKLMRAGEGKILRKLHRIADQVSSIEEDFVNLSDAELRALTDEYKERYADGESLDDLLPEAFATVREAAKRVLGQRHYDVQMMGGAALHLGYVAEMKTGEGKTLVGTLPAYLNALSGKGVHLITVNDYLAERDSELMGRVHKFLGLSVGCIVANMTPAQRREQYGCDITYGTNNEFGFDYLRDNMAWSKDELVQRGHNFAVVDEVDSILVDEARTPLIISGPADQATKWYGDFAKLVTRLTKGEAGNQLKGIEETGDYEVDEKKRTVAIHESGVAKVEDWLGIDNLYESVNTPLVGYLNNAIKAKELFKKDKDYVVIDGEVMIVDEHTGRILAGRRYNEGMHQAIEAKEGVDIKDENQTLATITLQNFFRLYDKLSGMTGTAMTEAAEFHQIYKLGVVPIPTNRPMVRADQSDLIYRTEVAKFAAVVDDIAEKHEKGQPILVGTTSVEKSEYLSQQLSKRGVQHEVLNAKQHDREATIVAQAGRKGAVTVATNMAGRGTDIKLGGNPDDLAEAELRQRGLDPVENVEEWAAALPAALEAAEQAVKAEFEEVKDLGGLYVLGTERHESRRIDNQLRGRSGRQGDPGESRFYLSLGDDLMRLFKAQMVERVMSMANVPDDVPIENKMVTRAIASAQSQVEQQNFETRKNVLKYDEVLNRQREVIYGERRRVLEGEDLQDQIRHFMDDTIDDYIRQETAEGFAEEWDLDRLWGAFRQLYPVKVTVDELEEAAGDLAGVTAEFIAESVKNDIHEQYEERENTLGSDIMRELERRVVLSVLDRKWREHLYEMDYLQEGIGLRAMAQKDPLVEYQREGFDMFNAMMEGIKEESVGYLFNLEVQVEQQVEEVPVQDGAERPSLEKEGAAAAPQIRAKGLEAPQRPDRLHFSAPTVDGEGGVVEGDFANDDASGATRSADGMTRAERRKAQKSGGGGGRRRKK
>NZ_CP010833.1|WP_075266011.1|5000416_5001037_-|GNAT-family-N-acetyltransferase
MEPITLTTERLVLRPFGPQDTHRVHAACQDPDIQRWTVIPSPYRLTDAELFTTKLAPAGWQDDSAYGFALTLRETGTLVGALGIDRRSRPGTYEVGYWSTKEHRGNGYVTEAVLGSARWAFASLGADRLEWRAEIGNLASRAVALRAGFRLEGEQRSGLLNKGVRRDAWTAALLPSDLGLAGTHPYVPGRHAPRPDGAQDSVRRPA
>NZ_CP010833.1|WP_075266010.1|4999163_5000351_-|winged-helix-turn-helix-domain-containing-protein
MTPVPPPAVELSADQARRIALRAQGFLGAPDRRAGVPGVLRHLGAVQLDTISVLARSHELIPYARLGSVGRRTVEEAYWSGGRTFEYWSHAACILPVEEWPHFAFRRRAYRSRPHWHHDLPDGVYETVIKQLRDEGPLTATELGGAKNGGEWWDWSASKVAVERALMYGEVVCTERRGWKRVYDLAERAIPDALLHDELSDAECRRRLVALAGRSLGVGTRGDIADYHRLKGEEFDAVVADSGLVPVVVEGWTKPAWADPEALAKEPRGRHRTTLLSPFDSLIWERARTERIFGFTHRLEAYVPKQKRIHGYFAMPLLAGGKLLGRVDPAREGTTLVAKQASPAGPKAVAPMAEALVEAAAWVGCTDIRVDRVDPPELREPLRTEIGHALQRAFR
>NZ_CP010833.1|WP_075266009.1|4998381_4999137_+|response-regulator-transcription-factor
MADTFGPVRDANDSDDDTGAYTGADADGAARKEPIRVLVVDDHALFRRGLEIVLAQEEDIQVIGEAGDGSEAVDKAADLLPDIVLMDVRMPKRGGIEACTAIKEVAPSAKIIMLTISDEEADLYEAIKAGATGYLLKEISTDEVATAIRAVADGQSQISPSMASKLLTEFKSMIQRTDERRLVPAPRLTDRELEVLKLVATGMNNRDIAKELFISENTVKNHVRNILEKLQLHSRMEAVVYAMREKILEIR
>NZ_CP010833.1|WP_006124981.1|4997508_4998198_+|ribosome-associated-translation-inhibitor-RaiA
MDIVVKGRKTEVPERFRKHVAEKLKLDKIQKFDGKVISLDVEVSKEPNPRQADRSDRVEITLRSRGPVIRAEAAAGDPYAALDLATGKLEARLRKQHDKRYSRRGNGRLSAAEVGDVVPGVASFDEDGELVGDQSPAPVPTTKIGSLEVQGEGPLVMREKTHTAAPMSLDQALYEMELVGHDFYLFVDSETKEPSVVYRRHAYDYGVIHLRTDPLAADEAGGAGGALGG
>NZ_CP010833.1|WP_075266018.1|5012856_5013648_-|ABC-transporter-ATP-binding-protein
MAEDRNTPGDHRVPTVVVDDVHITYTVNGARTGKGSATSALSRLTSRRRTPGARQVHAVKGVSFAAYKGEAIGLIGSNGSGKSTLLKAVAGLLPPTRGKVHTQGQPSLLGVNAALMGDLTGERNVILGGLAMGMTREQIRARYDEIVDFSGINEKGDFITLPMRTYSSGMGARLRFSIAAAKSHDVLLIDEALSTGDAKFQRRSKDRIKELRAEAGTVFLVSHSNKSITETCDRALWLEAGTLRMDGPAEEVVKAYEAFTKRK
>NZ_CP010833.1|WP_107472816.1|5013640_5014561_-|ABC-transporter-permease
MTAPSQGAPATAVPTYAPGELAALAARHGLKVSGARPSLPQYVRQLWGRRHFITAFATAKLTAQYSRAKLGQIWQIMTPLLNATVYYFIFGVLMNTKHGVEDFVPFLVTGVFIWTFTSSSITAGTRAISGNIGLVRALHFPRASLPVALALQQLQQLLFSLGALTLILLAFGQYPRPTWLLAVPALALQALFNTGLSMTMARLTAKTPDIAQLTPFVLRTWMYSSGVMWSLDHLLAGDRVPRAVMVLLEYNPAALYINLMRYALIDSYTWEQLPHLAWAAAAGWALLCGVAGFVYFWKAEETYGRG
>NZ_CP010833.1|WP_075266020.1|5014752_5015373_+|TetR/AcrR-family-transcriptional-regulator
MLRAMTTERGTRRRAPAGAAVLREDVTDAIRAAVFEELAAVGFARMSIEGIARRAGVGKTAVYRRWKSKLALVLDLVAAVAAQGMPAPATGSLYGDVRAVLELAAYALRHPVASQVIPDLLVEAARNPEISDAIKAALLDQQQGVAAVVVREAVARGELPEGSDPDRALDLIVGPLYWRLVVVRGELPEGYLDDLAASAVAALKHT
>NZ_CP010833.1|WP_075266021.1|5015487_5016711_-|hypothetical-protein
MPLFSAASAASSAADLPPAATAGDGAEGAARPSLWLPSPFLVLGGLLWAVLSAAAWQAPLCCEAGLQAAVVERLRVNLLHPAFPMTDLPAVASAHYSPYALLQGLAARATGLSGPSVVALAASVNLLLLLTGIGRLTRLLTPNRWVPVLLLVPLGLIHWADPARWSAPTTFAVAVTLHLWAWTGRVAARVAEPGDPAPRRTPRWFEAAAIGVLLGLVLLVHPQTAIGAAIGCLTLIVFRTRTRIRPTVWRWAFAGVCAVTVAALWPYYNGLTAQRAPIDSLTTAPPAAEGAKTAGEPYAWATAYVPPGEVVLTDSRPAMYALAGHGAYVLADALPDAGLATTERQERSRAVAAYLDMSTPQARRNGITARYGVRWLLLTRHQRLPENATVLAFSPRTGEVLARVAAG
>NZ_CP010833.1|WP_075266022.1|5016799_5020525_-|glycosyltransferase
MKPPLVSVVVPVHNVEAYLEDCLRSVAEQTLDAIEVVMVDDGSTDGSARIAAEFAARDSRFRLIRQQNAGLSAARNTGVRHTTPTVPYLAFADSDDVVVHDAYERMTASLESSGSDLVTGNVWRLTGQGRQQAWQYRWLTGPRSRTHITRDPRLLADRVAWNKVFRRSFWDTHAFAFPEGRLYEDTPVMIPAHYLAGSVDVLAEHVYYWRVREGSITRRRTDVTGVRDRIAACEQVSAFLGGRDAAQRRAYDASCLRDDFGYFLDGLPMGGEAYRAAFLEGAGAFVDRAGPEVLEGLPVELRIKWRLVRERRLAELLELLAFERANGTGTFAVEGLPGRRRAVYPGVRGASARLARTDIPAVARLLEARWGADGKLRLRGYAYLRNLPAGSARRRPTVGMVRAERGRMVRPVPVRPVPAPEATVNSGQELHGYEHAGFEMVLDPDRLPATAEGGGRLVGLVLAAPGAVRRVAVRAQDAGADQPLVHDLGDGRRAVLDFLGGRLRLTVSRLRARAEGHRTVAVGTAGASLEIAGRLFDGTARPTRLVLTREDGEECSCAVAYGEGSGPQGGAPGADTGAPGPGWGTPGSGGGVPRPDGDAAGPDRLTFTARVPLAELAAVPPAVHRAPREVEAAGGARWRVRLLLDDGTCVPLPAAPDLPPPACADAGGDLVLDLAGLPYADRVEATPEGGLRISGTYALAAPGTGAGAADAPGGRLVLRHETLHEVVPVAEGEVIDATADVNGAPGALGSGVGTPGTHPALRFSALVAPPLPEGRWEVRLDDRPVRVLGSAAAQLPCGDGGGTALRLERRHGDRLSVVAPPDVQAAGRSAYGRRLLRAAHHPEQRTPGTPSSGRRTPGPSRASRTLPLPLPLRDTVLYAGGDSPRAVHAELVRRGTDAEHLWVTGTTPGRITHVPPGARAVPVHSAAWYEALARSRRIVTDEQLPVWFERRPGQTVVQTWHGTPLGRFGSGLADSLYADHQHLATLPQRSAQWSVLISPSRFATPLLRRSLAYEGEVLEAGSPANDVLFPPVRDKAAEEVRRGLGIPEEHRVVLYAPTYRDHLAHPPSAVSASSADRTAPGPYRWDPALDPHALARALGPGHTVLVRRHPRVTGSVPPGPGVLDVSHHPGAAGLLLIADVLVTDYAGLMFDFALTGRPMLFHTYDLEHYRDTVRGFCLDFETRAPGPLLVTTDEVAQALRDTATSAARHADAYESFRRDYCDLDHGGAAARVADRLLADAE
>NZ_CP010833.1|WP_075266023.1|5020626_5021814_+|CDP-glycerol-glycerophosphotransferase-family-protein
MAPRASVKRYVRRQVMRAAYRTDLRRPLDPNLAVYGAYWNRGVACNPAAIHAKARELAPHIRGVWAVSSRHRDRMPPGGPYVIEGSRPYWRAMATATYLVNNSSFPGGFTKRPGQRYLQTHHGTPLKTMGLDQRAYPELARKTDFAKILAHVGQWDFSLSANPHSTEVWDRVYPGSYQRLDLGYPRNDVYFTATAEDIAKIRAELGIHADQTALLYTPTHRDYREGFVPDLDPERLARELGTAYVVLVRAHYFYGRSVGLGSAPTGRVLDVTAHPRVEELCLAADALITDYSSLAFDYACLDRPIVVHAPDWDTYRTTRGTYFDLLSGRPGDTPGAVTTTFDELVEVFRTGEWRSPASAALRTAFRERFCPYDDGHAAERVVRRLFAVPFAPPSR
>NZ_CP010833.1|WP_075266024.1|5021854_5022679_+|methyltransferase-domain-containing-protein
MHRSAYEQMELCIKEYLPVEGPASGRGAYRVVDLGSRISGKQTRTHRALLARHPIDYFGVDVQDGPNVDAVMRKPYRIPARSNSADVVLSGQAFEHIPFFWASMLEIARILKPGGHAFITAPSRGHVHDAQDCWRYYPDGFRALAAHSRLELVEAYTDFPPQKGIWHDYRAIDKKAAYWGDSVGVFRKPRRYPRLTMFVVRESAVWWANRVGGVDGVPLPRPVDGRDRCGRPTAPVPEPASESASMPASESASAPDSVPTPASAPGTAPESMAG
>NZ_CP010833.1|WP_075268513.1|5022723_5023572_+|methyltransferase
MAWRNAVNGVLQQLTGYQLRRVPVPAARTAPAGSAPAPAAPAAAPAPAPKPKAKKPAPAFPADYDDEAKDIIRAVKPYSMTSPERLNAFILATRYIARHDIPGSIVECGVWRGGSMQACARTLLSLGETERDLYLFDTYEGMTPPTAEDLRRDGRPAQELLDAQGKDRPIWAVASLEDVKAGFGHVPYPQERVHYVQGRVEDTVPGQAPEQISILRLDTDWYASTKHELEHLYHRLVPGGVLLIDDYGYWQGSRQAVDEFLEKTGERLLLLRMDEGRIAVKP
>NZ_CP010833.1|WP_075266025.1|5023791_5027289_+|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MAPRLTVVVPLYNVEEYLGACLTSLAEQTMPDLEVVLVDDGSTDNGPALAQEFTEHDPRFRLFRQENAGLGAARNAGVREAHPGAEFLTFVDSDDVVPPGAYARMLAELDRSDSDFATGNVLRLRANGDLEQSPMFRKPMEKARPATHVTRDWILLGDRIACNKVFRRTFWDEHAFAFPTGVLYEDIAVVLPAHFLARSVDVVEEPVYHWRDRDGSITTRRAVPRGIRDRVTAVTTVSNFLAERASEGGAAEAGGTADAAEAKRRYDAHALSGDLWLFIEALPDGDAEFHEAFLEHAGAFASTVEPGVFAALPLHLRVKWQLIRERRLPELLALLADEKKDRDTFHVRGLLRPRAHHPAVRDPLPPAATALTTADLPVHAHLTEAVWRDGLLHLTGYAHVRNAPGGAPRLGWLRAGKRLVPLRLRPVGGDEATARSGRSLHRYDRAGFTAVVDPRTLARKAGGGRTTWKLEAVVVGAGRPRRGPMRLVGTPAPPAVTYTDERTRIVPVLSGNKLELRTERVAAVLTGQSAVEDAVRLEVKVLGDAGPVALRLTEWRTKETREFALRGSPGSRAADIPLSVFRGADDIWGVQLIGEEKPLTVAARPGGQDGRYALPGGREVYAAPNPSGDLVLTDRAVQPVVTSAVWERSGELVLEGAFPEPMGTAHELVLRHSGHQEEAVVEVERGDGDHFRAVIAPAAVEGPGGALPLAEGRWYLFLRTPGERDPEVYRPLRLSTPLHSTLPRQHHQNHRDFTLQRRYHDRLVLESGSALPAVDRGPYGQRVRRERYAVLRAVAPAATRPAVLYSSFDGRQFSDSPRAIHRELAARKPDIEHLWVVRDQQAAVPDGVRAVALHSAEWYQALARSRWIVTNTHLPEWFERAEGQCVVQTWHGTPLKRIGRDLAGTPHADAAYMASMERRSAQWSVLVSPNSFSTPVLRRAFGYGGEILECGYPRNDLLYASDRAKVAAAVRERLAIPEGRRVILYAPTWREDQPRKSGRYAPDLHLDLEHARDVLGDDHVLLVRRHYLVGGTVPDTDFVRDVSRHPDAAELLLISDALVTDYSSIMFDFAQTGRPMVFHTYDLAHYRDTLRGFCFDFEHRAPGPLIPDSAGIVAALRDPDAVTAGHREAYEQFREAFCDLDDGTAAARVVDRMLKSDQAVEGEQA
>NZ_CP010833.1|WP_075266026.1|5027285_5030150_+|CDP-glycerol:glycerophosphate-glycerophosphotransferase
MSDVSCVITGGGDGEGPGGADALRASVESVLGQSMRAAEALVVLASAADPAVRTTARTLASRAPERVRLVHADPAARTTGALRNAGLDAATGRYVLVLGSGERLQKHACRNLWQAGETSRADLIAGRWSRTADESGKEREPSWQGELFARSRTLTRFTEAPQLVVRDALVTGFCLRREAARRHGLRYEEDLAHGEILFGPIAAASVGRIALVRRLIVTGRAVPDRARDLVALVEAHRRVANTLVARGLPELREEREQAFHRDHLVPLVRSFPALPAVRRDRVAAAAARTLTGPVPPDLPPLERVAVSLLGRGDAEGVLAAAYALSRPATVCAPLTTGADGRVGWGGEGEEPVADITELGHQYRRFGEMRLMNRLTRCAAADGGRLLLEGRLVLPGHTGPAPGAPLTATLEFRARGGARAVAFPAEVVRHDGTGITWRARADVVRRLRPVGVRDTAWDARLIVEADGARSVSDLFAPQDQVAGAVRFAARPRLGRLAGDTWEPYITLKDHFALRLAARRRPARTAHRLIRYATHFRPARKAKLLARALRKRLDRYRSRGFKAPAYNTWLIRLPVRRGSVVFESHMGTCYGDSPRALYEEIRRQGLKLHATWSYDPSPAGFPDDARLVRRWSWRYLWALARAEYWVDNQGFPPHLRKPRHTTYLQTWHGSAYKRMGFDETRVRLQNAPQRERLQQAVDRFDHFLVRSEHDVNTLARAYRLPEARLLRTGYPRNDALIAERTRAETEGRLPRPPLAGALGLDDHKKTVLYAPTFRGGPGKQRKSRLLLDVREFAERFGDTHTLLVRAHYLESARLPVCPPGTVVDVSRHHDVSELLAITDVLVTDYSSIMFDFALLDRPVVLFAPDLEAYAAERGSYFDLREQAPGPVTATQDELFAALAELKKSDTRYADQRRSFAERFGAYDQGDAARAAVAAVFGTAASRGVRHTTDHDRGAGR

Crispr_ID: NZ_CP010833_17

• CRISPR_ID: NZ_CP010833_17
• CRISPR_location: 5027426-5027523
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_17

Consensus_repeat	Method
CGCCGACCCGGCCGTCCGCACCACCG	CRISPRCasFinder

spacers of NZ_CP010833_17

>17.1|5027452|46|NZ_CP010833|CRISPRCasFinder
CCCGCACGCTCGCCTCCCGCGCGCCCGAACGGGTCCGGCTCGTCCA

CRISPR arrays and Neighbor proteins around NZ_CP010833_17

CRISPR arrays

The CRISPR arrays of NZ_CP010833_17

>merge|NZ_CP010833|17|5027426-5027523|CRISPRCasFinder
CGCCGACCCGGCCGTCCGCACCACCGCCCGCACGCTCGCCTCCCGCGCGCCCGAACGGGTCCGGCTCGTCCACGCCGACCCGGCCGCCCGCACCACCG

>NZ_CP010833|17|16|5027426-5027523|CRISPRCasFinder
CGCCGACCCGGCCGTCCGCACCACCG	CCCGCACGCTCGCCTCCCGCGCGCCCGAACGGGTCCGGCTCGTCCA
CGCCGACCCGGCCGCCCGCACCACCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075266021.1|5015487_5016711_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266034.1|5046626_5047493_+|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	gnl|CDD|240430
NZ_CP010833.1|WP_075266023.1|5020626_5021814_+|CDP-glycerol-glycerophosphotransferase-family-protein	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_075266031.1|5037660_5041482_-|FHA-domain-containing-protein	unknown	unknown	gnl|CDD|274858
NZ_CP010833.1|WP_075266029.1|5033750_5034695_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP010833.1|WP_075268514.1|5034691_5035978_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP010833.1|WP_075268513.1|5022723_5023572_+|methyltransferase	unknown	unknown	gnl|CDD|377550
NZ_CP010833.1|WP_075266018.1|5012856_5013648_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213187
NZ_CP010833.1|WP_107472816.1|5013640_5014561_-|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_CP010833.1|WP_075266025.1|5023791_5027289_+|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_075266033.1|5043850_5045095_+|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP010833.1|WP_075266024.1|5021854_5022679_+|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|369777
NZ_CP010833.1|WP_032775042.1|5045188_5046295_+|peptide-chain-release-factor-2	unknown	unknown	gnl|CDD|234799
NZ_CP010833.1|WP_075266030.1|5036078_5037443_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_CP010833.1|WP_075266020.1|5014752_5015373_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|379883
NZ_CP010833.1|WP_075266017.1|5007571_5012587_+|NAD-glutamate-dehydrogenase	unknown	unknown	gnl|CDD|377452
NZ_CP010833.1|WP_075266022.1|5016799_5020525_-|glycosyltransferase	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_075266032.1|5041954_5043661_+|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP010833.1|WP_075266027.1|5030146_5031289_+|glycosyltransferase	unknown	unknown	gnl|CDD|340847
NZ_CP010833.1|WP_075266028.1|5031314_5033546_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075266034.1|5046626_5047493_+|LPXTG-cell-wall-anchor-domain-containing-protein	gnl|CDD|240430	PTZ00473, PTZ00473, Plasmodium Vir superfamily; Provisional.	2.46061e-08
NZ_CP010833.1|WP_075266028.1|5031314_5033546_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	2.82681e-113
NZ_CP010833.1|WP_075266031.1|5037660_5041482_-|FHA-domain-containing-protein	gnl|CDD|274858	TIGR03924, T7SS_EccC_a, type VII secretion protein EccCa. This model represents the N-terminal domain or EccCa subunit of the type VII secretion protein EccC as found in the Actinobacteria. Type VII secretion is defined more broadly as including secretion systems for ESAT-6-like proteins in the Firmicutes as well as in the Actinobacteria, but this family does not show close homologs in the Firmicutes. [Protein fate, Protein and peptide secretion and trafficking].	1.04891e-25
NZ_CP010833.1|WP_075266029.1|5033750_5034695_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.43594e-76
NZ_CP010833.1|WP_075268514.1|5034691_5035978_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.23329e-38
NZ_CP010833.1|WP_075268513.1|5022723_5023572_+|methyltransferase	gnl|CDD|377550	pfam05711, TylF, Macrocin-O-methyltransferase (TylF). This family consists of bacterial macrocin O-methyltransferase (TylF) proteins. TylF is responsible for the methylation of macrocin to produce tylosin. Tylosin is a macrolide antibiotic used in veterinary medicine to treat infections caused by Gram-positive bacteria and as an animal growth promoter in the swine industry. It is produced by several Streptomyces species. As with other macrolides, the antibiotic activity of tylosin is due to the inhibition of protein biosynthesis by a mechanism that involves the binding of tylosin to the ribosome, preventing the formation of the mRNA-aminoacyl-tRNA-ribosome complex. The structure of one representative sequence from this family, NovP, shows it to be an S-adenosyl-l-methionine-dependent O-methyltransferase that catalyzes the penultimate step in the biosynthesis of the aminocoumarin antibiotic novobiocin. Specifically, it methylates at 4-OH of the noviose moiety, and the resultant methoxy group is important for the potency of the mature antibiotic. It is likely that the key structural features of NovP are common to the rest of the family and include: a helical 'lid' region that gates access to the co-substrate binding pocket and an active centre that contains a 3-Asp putative metal binding site. A further conserved Asp probably acts as the general base that initiates the reaction by de-protonating the 4-OH group of the noviose unit.	2.12612e-42
NZ_CP010833.1|WP_075266023.1|5020626_5021814_+|CDP-glycerol-glycerophosphotransferase-family-protein	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	2.19285e-144
NZ_CP010833.1|WP_075266018.1|5012856_5013648_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	1.1021e-93
NZ_CP010833.1|WP_107472816.1|5013640_5014561_-|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	3.76496e-40
NZ_CP010833.1|WP_075266025.1|5023791_5027289_+|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.73601e-104
NZ_CP010833.1|WP_075266033.1|5043850_5045095_+|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.19189e-82
NZ_CP010833.1|WP_075266024.1|5021854_5022679_+|methyltransferase-domain-containing-protein	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	3.92254e-10
NZ_CP010833.1|WP_032775042.1|5045188_5046295_+|peptide-chain-release-factor-2	gnl|CDD|234799	PRK00578, prfB, peptide chain release factor 2; Validated.	0
NZ_CP010833.1|WP_075266030.1|5036078_5037443_-|extracellular-solute-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.20125e-28
NZ_CP010833.1|WP_075266020.1|5014752_5015373_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|379883	pfam16859, TetR_C_11, Bacterial transcriptional repressor C-terminal. This family of bacterial transcriptional repressors is characterized by the short approximately 50 amino acid stretch of residues constituting the helix-turn-helix DNA binding motif, around the YRFhY motif. The target proteins that are repressed are involved in the transcriptional control of multi-drug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. Another target protein is BetI, an osmoprotectant which controls the choline-glycine betaine pathway in E.coli.	8.71354e-22
NZ_CP010833.1|WP_075266017.1|5007571_5012587_+|NAD-glutamate-dehydrogenase	gnl|CDD|377452	pfam05088, Bac_GDH, Bacterial NAD-glutamate dehydrogenase. This family consists of several bacterial proteins which are closely related to NAD-glutamate dehydrogenase found in Streptomyces clavuligerus. Glutamate dehydrogenases (GDHs) are a broadly distributed group of enzymes that catalyze the reversible oxidative deamination of glutamate to ketoglutarate and ammonia.	0
NZ_CP010833.1|WP_075266022.1|5016799_5020525_-|glycosyltransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	1.77036e-80
NZ_CP010833.1|WP_075266027.1|5030146_5031289_+|glycosyltransferase	gnl|CDD|340847	cd03820, GT4_AmsD-like, amylovoran biosynthesis glycosyltransferase AmsD and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. AmSD in Erwinia amylovora has been shown to be involved in the biosynthesis of amylovoran, the acidic exopolysaccharide acting as a virulence factor. This enzyme may be responsible for the formation of galactose alpha-1,6 linkages in amylovoran.	2.66318e-81
NZ_CP010833.1|WP_075266032.1|5041954_5043661_+|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	9.23258e-104

Protein sequences

>NZ_CP010833.1|WP_075266025.1|5023791_5027289_+|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MAPRLTVVVPLYNVEEYLGACLTSLAEQTMPDLEVVLVDDGSTDNGPALAQEFTEHDPRFRLFRQENAGLGAARNAGVREAHPGAEFLTFVDSDDVVPPGAYARMLAELDRSDSDFATGNVLRLRANGDLEQSPMFRKPMEKARPATHVTRDWILLGDRIACNKVFRRTFWDEHAFAFPTGVLYEDIAVVLPAHFLARSVDVVEEPVYHWRDRDGSITTRRAVPRGIRDRVTAVTTVSNFLAERASEGGAAEAGGTADAAEAKRRYDAHALSGDLWLFIEALPDGDAEFHEAFLEHAGAFASTVEPGVFAALPLHLRVKWQLIRERRLPELLALLADEKKDRDTFHVRGLLRPRAHHPAVRDPLPPAATALTTADLPVHAHLTEAVWRDGLLHLTGYAHVRNAPGGAPRLGWLRAGKRLVPLRLRPVGGDEATARSGRSLHRYDRAGFTAVVDPRTLARKAGGGRTTWKLEAVVVGAGRPRRGPMRLVGTPAPPAVTYTDERTRIVPVLSGNKLELRTERVAAVLTGQSAVEDAVRLEVKVLGDAGPVALRLTEWRTKETREFALRGSPGSRAADIPLSVFRGADDIWGVQLIGEEKPLTVAARPGGQDGRYALPGGREVYAAPNPSGDLVLTDRAVQPVVTSAVWERSGELVLEGAFPEPMGTAHELVLRHSGHQEEAVVEVERGDGDHFRAVIAPAAVEGPGGALPLAEGRWYLFLRTPGERDPEVYRPLRLSTPLHSTLPRQHHQNHRDFTLQRRYHDRLVLESGSALPAVDRGPYGQRVRRERYAVLRAVAPAATRPAVLYSSFDGRQFSDSPRAIHRELAARKPDIEHLWVVRDQQAAVPDGVRAVALHSAEWYQALARSRWIVTNTHLPEWFERAEGQCVVQTWHGTPLKRIGRDLAGTPHADAAYMASMERRSAQWSVLVSPNSFSTPVLRRAFGYGGEILECGYPRNDLLYASDRAKVAAAVRERLAIPEGRRVILYAPTWREDQPRKSGRYAPDLHLDLEHARDVLGDDHVLLVRRHYLVGGTVPDTDFVRDVSRHPDAAELLLISDALVTDYSSIMFDFAQTGRPMVFHTYDLAHYRDTLRGFCFDFEHRAPGPLIPDSAGIVAALRDPDAVTAGHREAYEQFREAFCDLDDGTAAARVVDRMLKSDQAVEGEQA
>NZ_CP010833.1|WP_075268513.1|5022723_5023572_+|methyltransferase
MAWRNAVNGVLQQLTGYQLRRVPVPAARTAPAGSAPAPAAPAAAPAPAPKPKAKKPAPAFPADYDDEAKDIIRAVKPYSMTSPERLNAFILATRYIARHDIPGSIVECGVWRGGSMQACARTLLSLGETERDLYLFDTYEGMTPPTAEDLRRDGRPAQELLDAQGKDRPIWAVASLEDVKAGFGHVPYPQERVHYVQGRVEDTVPGQAPEQISILRLDTDWYASTKHELEHLYHRLVPGGVLLIDDYGYWQGSRQAVDEFLEKTGERLLLLRMDEGRIAVKP
>NZ_CP010833.1|WP_075266024.1|5021854_5022679_+|methyltransferase-domain-containing-protein
MHRSAYEQMELCIKEYLPVEGPASGRGAYRVVDLGSRISGKQTRTHRALLARHPIDYFGVDVQDGPNVDAVMRKPYRIPARSNSADVVLSGQAFEHIPFFWASMLEIARILKPGGHAFITAPSRGHVHDAQDCWRYYPDGFRALAAHSRLELVEAYTDFPPQKGIWHDYRAIDKKAAYWGDSVGVFRKPRRYPRLTMFVVRESAVWWANRVGGVDGVPLPRPVDGRDRCGRPTAPVPEPASESASMPASESASAPDSVPTPASAPGTAPESMAG
>NZ_CP010833.1|WP_075266023.1|5020626_5021814_+|CDP-glycerol-glycerophosphotransferase-family-protein
MAPRASVKRYVRRQVMRAAYRTDLRRPLDPNLAVYGAYWNRGVACNPAAIHAKARELAPHIRGVWAVSSRHRDRMPPGGPYVIEGSRPYWRAMATATYLVNNSSFPGGFTKRPGQRYLQTHHGTPLKTMGLDQRAYPELARKTDFAKILAHVGQWDFSLSANPHSTEVWDRVYPGSYQRLDLGYPRNDVYFTATAEDIAKIRAELGIHADQTALLYTPTHRDYREGFVPDLDPERLARELGTAYVVLVRAHYFYGRSVGLGSAPTGRVLDVTAHPRVEELCLAADALITDYSSLAFDYACLDRPIVVHAPDWDTYRTTRGTYFDLLSGRPGDTPGAVTTTFDELVEVFRTGEWRSPASAALRTAFRERFCPYDDGHAAERVVRRLFAVPFAPPSR
>NZ_CP010833.1|WP_075266022.1|5016799_5020525_-|glycosyltransferase
MKPPLVSVVVPVHNVEAYLEDCLRSVAEQTLDAIEVVMVDDGSTDGSARIAAEFAARDSRFRLIRQQNAGLSAARNTGVRHTTPTVPYLAFADSDDVVVHDAYERMTASLESSGSDLVTGNVWRLTGQGRQQAWQYRWLTGPRSRTHITRDPRLLADRVAWNKVFRRSFWDTHAFAFPEGRLYEDTPVMIPAHYLAGSVDVLAEHVYYWRVREGSITRRRTDVTGVRDRIAACEQVSAFLGGRDAAQRRAYDASCLRDDFGYFLDGLPMGGEAYRAAFLEGAGAFVDRAGPEVLEGLPVELRIKWRLVRERRLAELLELLAFERANGTGTFAVEGLPGRRRAVYPGVRGASARLARTDIPAVARLLEARWGADGKLRLRGYAYLRNLPAGSARRRPTVGMVRAERGRMVRPVPVRPVPAPEATVNSGQELHGYEHAGFEMVLDPDRLPATAEGGGRLVGLVLAAPGAVRRVAVRAQDAGADQPLVHDLGDGRRAVLDFLGGRLRLTVSRLRARAEGHRTVAVGTAGASLEIAGRLFDGTARPTRLVLTREDGEECSCAVAYGEGSGPQGGAPGADTGAPGPGWGTPGSGGGVPRPDGDAAGPDRLTFTARVPLAELAAVPPAVHRAPREVEAAGGARWRVRLLLDDGTCVPLPAAPDLPPPACADAGGDLVLDLAGLPYADRVEATPEGGLRISGTYALAAPGTGAGAADAPGGRLVLRHETLHEVVPVAEGEVIDATADVNGAPGALGSGVGTPGTHPALRFSALVAPPLPEGRWEVRLDDRPVRVLGSAAAQLPCGDGGGTALRLERRHGDRLSVVAPPDVQAAGRSAYGRRLLRAAHHPEQRTPGTPSSGRRTPGPSRASRTLPLPLPLRDTVLYAGGDSPRAVHAELVRRGTDAEHLWVTGTTPGRITHVPPGARAVPVHSAAWYEALARSRRIVTDEQLPVWFERRPGQTVVQTWHGTPLGRFGSGLADSLYADHQHLATLPQRSAQWSVLISPSRFATPLLRRSLAYEGEVLEAGSPANDVLFPPVRDKAAEEVRRGLGIPEEHRVVLYAPTYRDHLAHPPSAVSASSADRTAPGPYRWDPALDPHALARALGPGHTVLVRRHPRVTGSVPPGPGVLDVSHHPGAAGLLLIADVLVTDYAGLMFDFALTGRPMLFHTYDLEHYRDTVRGFCLDFETRAPGPLLVTTDEVAQALRDTATSAARHADAYESFRRDYCDLDHGGAAARVADRLLADAE
>NZ_CP010833.1|WP_075266021.1|5015487_5016711_-|hypothetical-protein
MPLFSAASAASSAADLPPAATAGDGAEGAARPSLWLPSPFLVLGGLLWAVLSAAAWQAPLCCEAGLQAAVVERLRVNLLHPAFPMTDLPAVASAHYSPYALLQGLAARATGLSGPSVVALAASVNLLLLLTGIGRLTRLLTPNRWVPVLLLVPLGLIHWADPARWSAPTTFAVAVTLHLWAWTGRVAARVAEPGDPAPRRTPRWFEAAAIGVLLGLVLLVHPQTAIGAAIGCLTLIVFRTRTRIRPTVWRWAFAGVCAVTVAALWPYYNGLTAQRAPIDSLTTAPPAAEGAKTAGEPYAWATAYVPPGEVVLTDSRPAMYALAGHGAYVLADALPDAGLATTERQERSRAVAAYLDMSTPQARRNGITARYGVRWLLLTRHQRLPENATVLAFSPRTGEVLARVAAG
>NZ_CP010833.1|WP_075266020.1|5014752_5015373_+|TetR/AcrR-family-transcriptional-regulator
MLRAMTTERGTRRRAPAGAAVLREDVTDAIRAAVFEELAAVGFARMSIEGIARRAGVGKTAVYRRWKSKLALVLDLVAAVAAQGMPAPATGSLYGDVRAVLELAAYALRHPVASQVIPDLLVEAARNPEISDAIKAALLDQQQGVAAVVVREAVARGELPEGSDPDRALDLIVGPLYWRLVVVRGELPEGYLDDLAASAVAALKHT
>NZ_CP010833.1|WP_107472816.1|5013640_5014561_-|ABC-transporter-permease
MTAPSQGAPATAVPTYAPGELAALAARHGLKVSGARPSLPQYVRQLWGRRHFITAFATAKLTAQYSRAKLGQIWQIMTPLLNATVYYFIFGVLMNTKHGVEDFVPFLVTGVFIWTFTSSSITAGTRAISGNIGLVRALHFPRASLPVALALQQLQQLLFSLGALTLILLAFGQYPRPTWLLAVPALALQALFNTGLSMTMARLTAKTPDIAQLTPFVLRTWMYSSGVMWSLDHLLAGDRVPRAVMVLLEYNPAALYINLMRYALIDSYTWEQLPHLAWAAAAGWALLCGVAGFVYFWKAEETYGRG
>NZ_CP010833.1|WP_075266018.1|5012856_5013648_-|ABC-transporter-ATP-binding-protein
MAEDRNTPGDHRVPTVVVDDVHITYTVNGARTGKGSATSALSRLTSRRRTPGARQVHAVKGVSFAAYKGEAIGLIGSNGSGKSTLLKAVAGLLPPTRGKVHTQGQPSLLGVNAALMGDLTGERNVILGGLAMGMTREQIRARYDEIVDFSGINEKGDFITLPMRTYSSGMGARLRFSIAAAKSHDVLLIDEALSTGDAKFQRRSKDRIKELRAEAGTVFLVSHSNKSITETCDRALWLEAGTLRMDGPAEEVVKAYEAFTKRK
>NZ_CP010833.1|WP_075266017.1|5007571_5012587_+|NAD-glutamate-dehydrogenase
MQTKLDEAKAELLAGAAKVADNGPGGGVGGPGGAPRARASAGGADAGASAGQDTVLAYLQRYYLHTAPEDLSGRDPVDVFGAAASHYRLAENRPQGTANVRVHTPTVEENGWACSHSVVEVVTDDMPFLVDSVTNELSRQDRGIHLVIHPQVTVRRDVAGKLIEVLSGGPGTPKASQGRKKSKDAKGEKSELPHDALVESWIHVEIDRETDRADLQQITADLLRVLSDVRETVEDWGKMRDAALRIADDLPGEPLDDLADEEVEEARELLRWLAADHFTFLGYREYELKDSDALAAVPGTGLGILRSDPQHSEDEAHPVSPSFDRLPADVRAKAREHKLLVLTKANSRATVHRPSYLDYVGVKKFDAKGNVVGERRFLGLFSSAAYTESVRRVPVIRRKVAEVVEGAGFSYNSHDGRDLLQILETYPRDELFQTPVDQLRAVATSVLYLQERRRLRLYLRQDEYGRYYSAIVYLPRDRYTTGVRLRLIDILKEELGGTSVDFTAWNTESILSRLHFVIRVPAGTELPHLTDADADRIEARLVEAARSWADGFGEALTAELGEERAAELNRQYGHSFPEGYKADHSPRAAVSDLVHLETLREGEKDFALSLYEPVGAGPGERRFKIYRTGEQVSLSAVLPALQQLGVEVVDERPYELRCADRTHAWIYDFGLRMPLVNGNGGYLADDARARFQEAFAAVWKGEAENDGFNALVLGAGLNWRQAMVLRAYAKYLRQAGSTFSQDYMESTLRNNVHTTRLLVSLFEARMSPGRQSAGTELTDGLLEELDGALDQVASLDEDRILRSFLTVIKATLRTNFFQHTEDGEPHSYVSMKFDPQAIPDLPAPRPAFEIWVYSPRVEGVHLRFGKVARGGLRWSDRREDFRTEILGLVKAQMVKNTVIVPVGAKGGFVAKQLPDPSVDRDAWFAEGIAAYRTFISALLDITDNMVAGEVVPPTDVVRHDEDDTYLVVAADKGTASFSDIANEVAVAYGFWLGDAFASGGSAGYDHKGMGITARGAWESVKRHFRELGHDTQTEDFTVVGVGDMSGDVFGNGMLLSEHIRLVAAFDHRHIFIDPNPDAATSYAERRRLFDLPRSSWADYDTDLLSAGGGIHPRSAKSIPLNAHIREALGIDASVSKMTPADLMQTILKSPVDLVWNGGIGTYIKAVSESNADVGDKANDAIRVNGEDLRAKVVGEGGNLGATQLGRIEFARNGGRINTDAIDNSAGVDTSDHEVNIKILLNGLVRDGDMTVKQRNKLLADMTDEVGALVLRNNYAQNVALSNASAQAPSLLHAQQRFMRRLERDGALDRALEFLPADRHIRELLSNEKGLSQPELAVLLAYTKITTADELISTVLPDDPHLQKLVHAYFPSALRERFPEAVDGHALRREIITTVLVNDTVNTAGSTFLHRLREETGASIEEIVRAQFTAREIFGLSQVWDAVEALDNKVAADVQTRIRLHSRRLVERGSRWLLGNRPQPVAISETIDLFRDGVEQVWNELPKLVRGADLDWYHSILDELTAAGVPDGLAVRVAGFSSAFPALDIVAIADRTGKEPLEVAEVYYDLADRLRITQLMDRIIELPRADRWQSMARASIREDLYAAHAALTSDVLSVGNGSSTPEERFRAWEEKNAAILARSRSTLEEIQGSDAFDLANLSVAMRTMRTLLRTHA
>NZ_CP010833.1|WP_075266027.1|5030146_5031289_+|glycosyltransferase
MSRDIFIVSNSTDELGGVTGWMHQTARLFADQGHRVHTVGIHASDLKMTLPRQPDHPVTALYAAHPPTPWTPHGVRDRFRIPTRRKEAARVAAKRQAVGRLSELFATARPGAVVIVTQVWAMEWVGEADTTGLRVIGMSHESYDYSRASHRYRWIKNHYKDLDHWLVLTEEDADRWAGDGMNNVGFLPNALSRLPLVPSARTAKTVASIGRLSDQKGIDLLLDSWALVAPARPDWTLRVYGAGEDEAALKAQCTGLGLDGSVEWMGRTDDVERALAGSSVFVQSSRGEGFPLALLEAMASGVPCAAFDCAPGVREIVRDGEDGLLAPAGDVAALADRLLRLTGNPRLRDAMGARARSGVQRFSEPETLRRWEELFAFLER
>NZ_CP010833.1|WP_075266028.1|5031314_5033546_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MPRFSVIVPAFRVQAYLHACLDSVLAQSFKDYEIVVVDDCSPDACGPIADEYARRDPRVTALHLPRNIGLGPARNAGMGRAAGDYLIFLDGDDTLLPDALQTIADRIDATGEPDVLMYDYARTYWTGRSVRNVLAAHLDESGPERFRLTDRPELLRLLMVVWNKAYRRAFVEAEGFTFPPGYYEDTPWTYPVLMAADSIAVLDAVCVSYRQRRRGNILSTTSEKHFDVFDQYDRVFAFIDSRPELALWRPVIFRRMLDHFAALFASRDRLPLHSRAAFFRRATASCRRHHTPGAPAPRRALLRHGLMHLGARRTYRALSEAQRLGGRLRKGAAALRRAVRGAALRAHYRIQLRLPLRTRDAVFTTRAGSGYAGSPAAVEAKVRELVPGVRTAWVCRPADAHTVPTGTRHLAPGTFAHRTALARSAYLVNDGPFDRGLVKRRGQILLQTHEGTPLRTEGTDLLDRPAAARGTDFDELLRQVDTWDFSLSANPHSTLVRERAYPSAYTTLEYGSPRNDVYHRSDPADVARLRETLGIPEGATALLYAPVPRDYRRVQRPSLDLERLVRVLGPQFVILARVPRPAGPGVRGRAAHPRIIDVSAHRSVETLALASDALLTDYASLMFDYVNLDRPVVLHLDDIEAYEASRGTYFDITAFPPGVVARSQDELFDIFATDHWRGSRSAQLRAAFRARFCPYDDGYAAERVVRRVFLGETDGLPLPVPFPARRTPAALPAQDGAGAAVGG
>NZ_CP010833.1|WP_075266029.1|5033750_5034695_-|carbohydrate-ABC-transporter-permease
MSSAPDVNTARIGRQKAVTRKTGGTPEAPKAEQSLGARIAARAGGGVMRVFLVLVALFWLMPTIGLLLSSLRGPQDIAATGWWKIFTAPSELTFENYQRLLDNATITGSLGSTIMITVPSTVLVVLIGSFAGYAFAWMEFPGRDWLFLLVVGLLVVPVQVALIPVSELFGTIGIFETTLGVVLFHTAFGLPFAIFLLRNFFAEIPRELLEAARLDGAGEIRLFTRVVMPLGGPAIASLGIFQFLWVWNDMLVALIFADSESPPITVALQQQVRQFGNNIDVLAPGAFVSMVIPLAVFFAFQRQFVSGVMAGAVK
>NZ_CP010833.1|WP_075268514.1|5034691_5035978_-|sugar-ABC-transporter-permease
MTGTRRIVAAVFLLPALVLLGALVLYPIGYSVYRSFFDQAGTGFAGFDNYEALFTDDTIRTAVKNNAIWVVFAPTVATALGLIFAVLTERIRWGTAFKLIVFMPMAISMLAAGIIFRLVYDQAPERGVANAVAVSVHDTFNESAGFPKARPLPVHPLEKAAGGTFVSKEPIRAGEPLRVPLVGVAPAKMPGDARPAEGAPAASGDRISGTAWLDFTRGGGGKPNVVDPKELGLKGLKVEAVKDGKVVATATAGADGVFTLPASADGAQLRLPADNFREPYNGVDWLGPSLVTPGIIGSYVWMWAGFAMVLIAAGLAGLPRELLEAARVDGANEWQVFRRITVPMLAPVLAVVLVTLMINVLKVFDLVFIIAPGSSQDDANVLALQLYRSSFGTDADLGIGSAIAVLLLLLVIPVMLVNIRRIRKEGRR
>NZ_CP010833.1|WP_075266030.1|5036078_5037443_-|extracellular-solute-binding-protein
MRTTFSIRRTAVVFAAVGALALTGCGGDGDGKKKSGDDSGKGADSASTVDLPKLDGEKVSVAAVWTGPEQANFTKVLDEFEKRTGADVTFVPAQDPIINFLGTKIAGKQPPDVAMIPQVGAVQQAAAKKWAKPVGPEAKAQLDKNYAKVWQDLGAVDGTQYGVYFKAANKSLIWYNAAAFDNAGASEPKTWKDFLTTAETISASGVTPVSVGGADGWTLTDWFENVYLSQAGPEKYDQLAKHEIPWTDPSVKDALTTLAELFGKPELIAGGADGALQTEFPASVTQTFTGGDQPKGAMVFEGDFVAVNIAQTEAKIGTDAKVFPFPAVGADSPVVTGGDAAVALKDSKGAQALLTWLASADAAKIWAEAGGFISPNKGLDLKAYPNDVQRTMAQALIDAGDDVRFDMSDQAPQSFGGTPGAGEWKILQDFLKNPKDIAGTQKKLESEAVKAYKS
>NZ_CP010833.1|WP_075266031.1|5037660_5041482_-|FHA-domain-containing-protein
MQIRLTVLAPRSGQTPARTCDVLVTAPAGTALAAVASQLAAAVSGPESSQGGGAVVLFAGRERLDGHRIALGEPPLVDGAVLSLQIPGDDEATDDAVPAQLHVVAGPDAGGVHLLHGGQIRIGRSADADVPLDDPDVSRLHCAVSVSDDGRVSVADLGSTNGTSLDGVEVRERPVRLAPGALLRLGESTLRLTSGSRPTTLPTAPDGEGHLRVTRAETGAADPGRGTDAPLTPRSSDHGGQGPHAYGAPASSPFASSEPSGAYGDPDPSFDETASWPEHAEAGPGGAYAGGGTPARGEEFAGTPAPRRGIGAWARRLKGGAKGGQAARPAAGAGAGERADAYGPARTPGARAAYGSPPYGTGADDSGSRGSGGHSSGGYGSGGHDPIGHGSGAGFPGVPGGAASPAGGPSGAGHLASPASPGSPFSALPSAPEGTWPDPAAVLLTALGPGPRLWERHPAHPEALVVRLGTTDRAEVPAVPVTVGLREAGSLGLAGPRARLAGLARATVAQLAALHSPFDLEIVLISTDRSRTLEERRREWSWLGWLPHLRPTHGQDCRLLLAYDREQAEARAAELVRRLDEGPLGPGWPHLDRAAVAEAARAHTGPHTVVVLDGDPGTAFLRETTARLAGAGAAAGIHLICLAETPSASPTSPVAATYEAACRGSIAFRECGAVAMLSGDVATALRLLRTAGGQAAGHGTVAAVDAVSAAWAERFGRALAPLREEGSAALAGRPTTAALPPSARLLDELGLARATPASLMARWASTAEAQPGASAPRAAAAPLPRADLDSPNSGRTLSAGPRVGPQRTAASPHHDSGRTPYPAAGAPDPDRTPYPPLDSRDSGRTPYPPLDSRDSGRTPYPPLDSRDSERTPHLGAQRSGPGRGAGNGSGSEAGVAAGERGDATLPVSGSGAAAPATVHAGRPVLVLGAGPRGPLSVDLADEGPHLLIEGPPGSGRTELLRAVAASLASAARPDRLGILLVDGSGGEQGERGEGLLPCTELPHVFTHLVASDPVRMREFAQALGGELKRRAELLGELDFADWHERYGQQGAQRGPAPRVVGQRPPSGAERRGDLDSPASGTLRLRPAAARSADPGPSPLPRLVVLADDFDALVAPALGSPGRPAAGSVVRALEAVARDGGRLGVHLVATSARPDRTEDTELARGARLRIVLDAPVLPPSPDEPAPGRGRLGHPDGRVTPFQGGRVTGRIPRTATLRPTVVPLEWERMGDPPTRRPVRELGNGPTDLALLASALERAARSVNAERLPALVPFTT
>NZ_CP010833.1|WP_075266032.1|5041954_5043661_+|serine/threonine-protein-kinase
MRPVGSKYLLEEPLGRGATGTVWRARQRETAGAEAAVAGQPGETVAIKVLKEELANDADVVMRFLRERSVLLRLTHPNIVRTRDLVVEGDLLALVMDLIDGPDLHRYLRENGPLTPVAAALLTAQIADALAASHADGVVHRDLKPANVLLDERDGGMTPMLTDFGIARLADSPGLTRTHEFVGTPAYVAPESAEGRPQTSAVDIYGAGILLYELVTGRPPFAGGTALEVLHRHLSEEPRRPSTVPGPLWTVIERCLSKDPDRRPSAENLARGLRTVASGIGVHANSAQIAAAEGVGALLAPDPAPTAVPDTPGAADPTQVLPSNAGSYDPAAATSVLPQTGPGGQGGPGQGPGGHADPTAVMPPVPQRPDGPPQPDGPHPWQSQLQAARDRNEQTQVQYLDPSQDPLRRRPQRQQPPQQQPPQRQQQPAQRRQQPLQQQYPYQQQQQQQQQQQQPQRYQQPQQPQRQQYAPPQPQQPQQPAARPPREPRQPRQRSANPMRIPGLGCLKGCLFTLILLIVAGWLIWELTPLQDWVAQGKGYWEAIGDGIAKVSDWFSELGDSAGGSGGA
>NZ_CP010833.1|WP_075266033.1|5043850_5045095_+|serine/threonine-protein-kinase
MARNIGSRYTAHQILGRGSAGTVWLGEGPEGPVAIKLLREDLASDQELVGRFVQERTALLGLDHPHVVAVRDLVVDGNDLALVMTLVRGTDLRTRLDRERRLAPEAAVAIIADVADGLAAAHKAQIVHRDVKPENILLDMEGPLGPGGAHPALLTDFGVAKLIDTPRRTKATKIIGTPDYLAPEIVEGLPPRAAVDIYALATVLYELLAGFTPFGGGHPGAVLRRHVTETVVPLPGIPEELWQLLVQCLAKAPASRLRASELAVRLRDLLPLLAGIPPLEVDEPGPEESERAPSYDEQQYTPAADEPRRRGAVPLVPGSAPDSNRDTHTSMRVPAPDELAGGPLGTARAPRAPGRPRPGSARNKAVSVRKRRITLGAAAVLLCAAVAVGGWLATGGGDGGGAPQDSENSAPATP
>NZ_CP010833.1|WP_032775042.1|5045188_5046295_+|peptide-chain-release-factor-2
MAVVDISEELKSLSSTMGSIEAVLDLDALRADIAALEEQAAAPSLWDDPDAAQKITSKLSHLQAEVRKAEALRGRIDDLEVLFELAEAEGDADARAEAEAELESVKKALDEMEVRTLLSGEYDAREALVTIRAEAGGVDAADFAEKLQRMYLRWAEQHNYKTEVYETAYAEEAGIKSTTFAVQVPYAYGTLSVEQGTHRLVRISPFDNQGRRQTSFAGVEVLPVVEQTDHIEIDESELRVDVYRSSGPGGQGVNTTDSAVRLTHLPTGIVVSCQNERSQIQNKASAMNVLQAKLLERRRQEEQAKMNALKGDGGNSWGNQMRSYVLHPYQMVKDLRTEFEMGNPEAVFNGEIDGFVEAGIRWRKQREK
>NZ_CP010833.1|WP_075266034.1|5046626_5047493_+|LPXTG-cell-wall-anchor-domain-containing-protein
MTKKTRVRVARIAAGAVIAAGASLTAAGAAQALEIGVDTGVAEVNVQADLLDGDDPIGGADPGGAAGETTTGETTGETTTGETTTGETTTGETTGETSTTGETTTGETTGETSTTGETSTTGETSTTGETSTTGETTTGETTGETSTTGETSTTGETSTTGETSTTGETSTGTTGSTGTSGSTGTSGSTGTTGSTGGDQGGSSATGGSTTGGDDAGCTVDLDGAECTDNTDTDSVGNKPVEQSKGKEELAETGAAETTFLVIGAATMIAGGIGFRILPRLVGGGRTVA

Crispr_ID: NZ_CP010833_18

• CRISPR_ID: NZ_CP010833_18
• CRISPR_location: 5046825-5047132
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 5 spacers

Consensus repeat of NZ_CP010833_18

Consensus_repeat	Method
GNNNNGNCCACCACGGGTGAGAC	CRT

spacers of NZ_CP010833_18

>18.1|5046848|19|NZ_CP010833|CRT
GACCGGCGAGACCACCACC
>18.2|5046890|37|NZ_CP010833|CRT
CACGACCGGTGAGACCACGGGCGAGACGTCCACCACG
>18.3|5046950|43|NZ_CP010833|CRT
GACCGGCGAGACGTCCACCACCGGTGAGACCTCGACGACCGGC
>18.4|5047016|40|NZ_CP010833|CRT
CTCGACCACGGGTGAGACCACCACGGGTGAGACGACCGGC
>18.5|5047079|31|NZ_CP010833|CRT
CTCGACGACCGGCGAGACGTCCACCACGGGT

CRISPR arrays and Neighbor proteins around NZ_CP010833_18

CRISPR arrays

The CRISPR arrays of NZ_CP010833_18

>merge|NZ_CP010833|18|5046825-5047132|CRT
GGTGAGACCACCACGGGTGAGACGACCGGCGAGACCACCACCGGTGAGACCACCACGGGCGAGACCACGACCGGTGAGACCACGGGCGAGACGTCCACCACGGGTGAGACCACCACGGGTGAGACGACCGGCGAGACGTCCACCACCGGTGAGACCTCGACGACCGGCGAGACGTCCACCACGGGTGAGACCTCGACCACGGGTGAGACCACCACGGGTGAGACGACCGGCGAGACGTCCACCACCGGTGAGACCTCGACGACCGGCGAGACGTCCACCACGGGTGAGACCTCGACCACGGGTGAGAC

>NZ_CP010833|18|3|5046825-5047132|CRT
GGTGAGACCACCACGGGTGAGAC	GACCGGCGAGACCACCACC
GGTGAGACCACCACGGGCGAGAC	CACGACCGGTGAGACCACGGGCGAGACGTCCACCACG
GGTGAGACCACCACGGGTGAGAC	GACCGGCGAGACGTCCACCACCGGTGAGACCTCGACGACCGGC
GAGACGTCCACCACGGGTGAGAC	CTCGACCACGGGTGAGACCACCACGGGTGAGACGACCGGC
GAGACGTCCACCACCGGTGAGAC	CTCGACGACCGGCGAGACGTCCACCACGGGT
GAGACCTCGACCACGGGTGAGAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_010070940.1|5047684_5047882_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266026.1|5027285_5030150_+|CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_159027441.1|5052126_5052291_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266031.1|5037660_5041482_-|FHA-domain-containing-protein	unknown	unknown	gnl|CDD|274858
NZ_CP010833.1|WP_075266029.1|5033750_5034695_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP010833.1|WP_075266035.1|5049872_5051060_+|PDZ-domain-containing-protein	unknown	unknown	gnl|CDD|223864
NZ_CP010833.1|WP_075266027.1|5030146_5031289_+|glycosyltransferase	unknown	unknown	gnl|CDD|340847
NZ_CP010833.1|WP_075266038.1|5055638_5056334_+|hypothetical-protein	unknown	unknown	gnl|CDD|237030
NZ_CP010833.1|WP_003968790.1|5051078_5051567_+|SsrA-binding-protein-SmpB	unknown	unknown	gnl|CDD|376590
NZ_CP010833.1|WP_075266037.1|5054504_5055476_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_CP010833.1|WP_075268514.1|5034691_5035978_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP010833.1|WP_075266028.1|5031314_5033546_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	unknown	unknown	gnl|CDD|367953
NZ_CP010833.1|WP_003968787.1|5048142_5048832_+|cell-division-ATP-binding-protein-FtsE	unknown	unknown	gnl|CDD|225438
NZ_CP010833.1|WP_079181629.1|5053066_5054305_-|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP010833.1|WP_032775042.1|5045188_5046295_+|peptide-chain-release-factor-2	unknown	unknown	gnl|CDD|234799
NZ_CP010833.1|WP_075266030.1|5036078_5037443_-|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_CP010833.1|WP_075266039.1|5056334_5058551_+|glycosyltransferase	unknown	unknown	gnl|CDD|200584
NZ_CP010833.1|WP_075266033.1|5043850_5045095_+|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP010833.1|WP_010062141.1|5048886_5049804_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|225088
NZ_CP010833.1|WP_075266032.1|5041954_5043661_+|serine/threonine-protein-kinase	unknown	unknown	gnl|CDD|270916

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075266026.1|5027285_5030150_+|CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	3.29775e-101
NZ_CP010833.1|WP_075266031.1|5037660_5041482_-|FHA-domain-containing-protein	gnl|CDD|274858	TIGR03924, T7SS_EccC_a, type VII secretion protein EccCa. This model represents the N-terminal domain or EccCa subunit of the type VII secretion protein EccC as found in the Actinobacteria. Type VII secretion is defined more broadly as including secretion systems for ESAT-6-like proteins in the Firmicutes as well as in the Actinobacteria, but this family does not show close homologs in the Firmicutes. [Protein fate, Protein and peptide secretion and trafficking].	1.04891e-25
NZ_CP010833.1|WP_075266029.1|5033750_5034695_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.43594e-76
NZ_CP010833.1|WP_075266035.1|5049872_5051060_+|PDZ-domain-containing-protein	gnl|CDD|223864	COG0793, Prc, Periplasmic protease [Cell envelope biogenesis, outer membrane].	7.5643e-62
NZ_CP010833.1|WP_075266027.1|5030146_5031289_+|glycosyltransferase	gnl|CDD|340847	cd03820, GT4_AmsD-like, amylovoran biosynthesis glycosyltransferase AmsD and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. AmSD in Erwinia amylovora has been shown to be involved in the biosynthesis of amylovoran, the acidic exopolysaccharide acting as a virulence factor. This enzyme may be responsible for the formation of galactose alpha-1,6 linkages in amylovoran.	2.66318e-81
NZ_CP010833.1|WP_075266038.1|5055638_5056334_+|hypothetical-protein	gnl|CDD|237030	PRK12270, kgd, multifunctional oxoglutarate decarboxylase/oxoglutarate dehydrogenase thiamine pyrophosphate-binding subunit/dihydrolipoyllysine-residue succinyltransferase subunit.	2.68341e-07
NZ_CP010833.1|WP_003968790.1|5051078_5051567_+|SsrA-binding-protein-SmpB	gnl|CDD|376590	pfam01668, SmpB, SmpB protein.	3.53593e-86
NZ_CP010833.1|WP_075266037.1|5054504_5055476_+|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	5.01686e-26
NZ_CP010833.1|WP_075268514.1|5034691_5035978_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.23329e-38
NZ_CP010833.1|WP_075266028.1|5031314_5033546_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase	gnl|CDD|367953	pfam04464, Glyphos_transf, CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase. Wall-associated teichoic acids are a heterogeneous class of phosphate-rich polymers that are covalently linked to the cell wall peptidoglycan of gram-positive bacteria. They consist of a main chain of phosphodiester-linked polyols and/or sugar moieties attached to peptidoglycan via a linkage unit. CDP-glycerol:poly(glycerophosphate) glycerophosphotransferase is responsible for the polymerization of the main chain of the teichoic acid by sequential transfer of glycerol-phosphate units from CDP-glycerol to the linkage unit lipid.	2.82681e-113
NZ_CP010833.1|WP_003968787.1|5048142_5048832_+|cell-division-ATP-binding-protein-FtsE	gnl|CDD|225438	COG2884, FtsE, Predicted ATPase involved in cell division [Cell division and chromosome partitioning].	2.2302e-124
NZ_CP010833.1|WP_079181629.1|5053066_5054305_-|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.20366e-14
NZ_CP010833.1|WP_032775042.1|5045188_5046295_+|peptide-chain-release-factor-2	gnl|CDD|234799	PRK00578, prfB, peptide chain release factor 2; Validated.	0
NZ_CP010833.1|WP_075266030.1|5036078_5037443_-|extracellular-solute-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.20125e-28
NZ_CP010833.1|WP_075266039.1|5056334_5058551_+|glycosyltransferase	gnl|CDD|200584	cd10962, CE4_GT2-like, Catalytic NodB homology domain of uncharacterized bacterial glycosyl transferase, group 2-like family proteins. This family includes many uncharacterized bacterial proteins containing an N-terminal GH18 (glycosyl hydrolase, family 18) domain, a middle NodB-like homology domain, and a C-terminal GT2-like (glycosyl transferase group 2) domain. Although their biological function is unknown, members in this family contain a middle NodB homology domain that is similar to the catalytic domain of Streptococcus pneumoniae polysaccharide deacetylase PgdA (SpPgdA), an extracellular metal-dependent polysaccharide deacetylase with de-N-acetylase activity toward a hexamer of chitooligosaccharide N-acetylglucosamine, but not shorter chitooligosaccharides or a synthetic peptidoglycan tetrasaccharide. Like SpPgdA, this family is a member of the carbohydrate esterase 4 (CE4) superfamily. The presence of three domains suggests that members of this family may be multifunctional.	2.159e-88
NZ_CP010833.1|WP_075266033.1|5043850_5045095_+|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.19189e-82
NZ_CP010833.1|WP_010062141.1|5048886_5049804_+|ABC-transporter-permease	gnl|CDD|225088	COG2177, FtsX, Cell division protein [Cell division and chromosome partitioning].	6.63169e-60
NZ_CP010833.1|WP_075266032.1|5041954_5043661_+|serine/threonine-protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	9.23258e-104

Protein sequences

>NZ_CP010833.1|WP_032775042.1|5045188_5046295_+|peptide-chain-release-factor-2
MAVVDISEELKSLSSTMGSIEAVLDLDALRADIAALEEQAAAPSLWDDPDAAQKITSKLSHLQAEVRKAEALRGRIDDLEVLFELAEAEGDADARAEAEAELESVKKALDEMEVRTLLSGEYDAREALVTIRAEAGGVDAADFAEKLQRMYLRWAEQHNYKTEVYETAYAEEAGIKSTTFAVQVPYAYGTLSVEQGTHRLVRISPFDNQGRRQTSFAGVEVLPVVEQTDHIEIDESELRVDVYRSSGPGGQGVNTTDSAVRLTHLPTGIVVSCQNERSQIQNKASAMNVLQAKLLERRRQEEQAKMNALKGDGGNSWGNQMRSYVLHPYQMVKDLRTEFEMGNPEAVFNGEIDGFVEAGIRWRKQREK
>NZ_CP010833.1|WP_075266033.1|5043850_5045095_+|serine/threonine-protein-kinase
MARNIGSRYTAHQILGRGSAGTVWLGEGPEGPVAIKLLREDLASDQELVGRFVQERTALLGLDHPHVVAVRDLVVDGNDLALVMTLVRGTDLRTRLDRERRLAPEAAVAIIADVADGLAAAHKAQIVHRDVKPENILLDMEGPLGPGGAHPALLTDFGVAKLIDTPRRTKATKIIGTPDYLAPEIVEGLPPRAAVDIYALATVLYELLAGFTPFGGGHPGAVLRRHVTETVVPLPGIPEELWQLLVQCLAKAPASRLRASELAVRLRDLLPLLAGIPPLEVDEPGPEESERAPSYDEQQYTPAADEPRRRGAVPLVPGSAPDSNRDTHTSMRVPAPDELAGGPLGTARAPRAPGRPRPGSARNKAVSVRKRRITLGAAAVLLCAAVAVGGWLATGGGDGGGAPQDSENSAPATP
>NZ_CP010833.1|WP_075266032.1|5041954_5043661_+|serine/threonine-protein-kinase
MRPVGSKYLLEEPLGRGATGTVWRARQRETAGAEAAVAGQPGETVAIKVLKEELANDADVVMRFLRERSVLLRLTHPNIVRTRDLVVEGDLLALVMDLIDGPDLHRYLRENGPLTPVAAALLTAQIADALAASHADGVVHRDLKPANVLLDERDGGMTPMLTDFGIARLADSPGLTRTHEFVGTPAYVAPESAEGRPQTSAVDIYGAGILLYELVTGRPPFAGGTALEVLHRHLSEEPRRPSTVPGPLWTVIERCLSKDPDRRPSAENLARGLRTVASGIGVHANSAQIAAAEGVGALLAPDPAPTAVPDTPGAADPTQVLPSNAGSYDPAAATSVLPQTGPGGQGGPGQGPGGHADPTAVMPPVPQRPDGPPQPDGPHPWQSQLQAARDRNEQTQVQYLDPSQDPLRRRPQRQQPPQQQPPQRQQQPAQRRQQPLQQQYPYQQQQQQQQQQQQPQRYQQPQQPQRQQYAPPQPQQPQQPAARPPREPRQPRQRSANPMRIPGLGCLKGCLFTLILLIVAGWLIWELTPLQDWVAQGKGYWEAIGDGIAKVSDWFSELGDSAGGSGGA
>NZ_CP010833.1|WP_075266031.1|5037660_5041482_-|FHA-domain-containing-protein
MQIRLTVLAPRSGQTPARTCDVLVTAPAGTALAAVASQLAAAVSGPESSQGGGAVVLFAGRERLDGHRIALGEPPLVDGAVLSLQIPGDDEATDDAVPAQLHVVAGPDAGGVHLLHGGQIRIGRSADADVPLDDPDVSRLHCAVSVSDDGRVSVADLGSTNGTSLDGVEVRERPVRLAPGALLRLGESTLRLTSGSRPTTLPTAPDGEGHLRVTRAETGAADPGRGTDAPLTPRSSDHGGQGPHAYGAPASSPFASSEPSGAYGDPDPSFDETASWPEHAEAGPGGAYAGGGTPARGEEFAGTPAPRRGIGAWARRLKGGAKGGQAARPAAGAGAGERADAYGPARTPGARAAYGSPPYGTGADDSGSRGSGGHSSGGYGSGGHDPIGHGSGAGFPGVPGGAASPAGGPSGAGHLASPASPGSPFSALPSAPEGTWPDPAAVLLTALGPGPRLWERHPAHPEALVVRLGTTDRAEVPAVPVTVGLREAGSLGLAGPRARLAGLARATVAQLAALHSPFDLEIVLISTDRSRTLEERRREWSWLGWLPHLRPTHGQDCRLLLAYDREQAEARAAELVRRLDEGPLGPGWPHLDRAAVAEAARAHTGPHTVVVLDGDPGTAFLRETTARLAGAGAAAGIHLICLAETPSASPTSPVAATYEAACRGSIAFRECGAVAMLSGDVATALRLLRTAGGQAAGHGTVAAVDAVSAAWAERFGRALAPLREEGSAALAGRPTTAALPPSARLLDELGLARATPASLMARWASTAEAQPGASAPRAAAAPLPRADLDSPNSGRTLSAGPRVGPQRTAASPHHDSGRTPYPAAGAPDPDRTPYPPLDSRDSGRTPYPPLDSRDSGRTPYPPLDSRDSERTPHLGAQRSGPGRGAGNGSGSEAGVAAGERGDATLPVSGSGAAAPATVHAGRPVLVLGAGPRGPLSVDLADEGPHLLIEGPPGSGRTELLRAVAASLASAARPDRLGILLVDGSGGEQGERGEGLLPCTELPHVFTHLVASDPVRMREFAQALGGELKRRAELLGELDFADWHERYGQQGAQRGPAPRVVGQRPPSGAERRGDLDSPASGTLRLRPAAARSADPGPSPLPRLVVLADDFDALVAPALGSPGRPAAGSVVRALEAVARDGGRLGVHLVATSARPDRTEDTELARGARLRIVLDAPVLPPSPDEPAPGRGRLGHPDGRVTPFQGGRVTGRIPRTATLRPTVVPLEWERMGDPPTRRPVRELGNGPTDLALLASALERAARSVNAERLPALVPFTT
>NZ_CP010833.1|WP_075266030.1|5036078_5037443_-|extracellular-solute-binding-protein
MRTTFSIRRTAVVFAAVGALALTGCGGDGDGKKKSGDDSGKGADSASTVDLPKLDGEKVSVAAVWTGPEQANFTKVLDEFEKRTGADVTFVPAQDPIINFLGTKIAGKQPPDVAMIPQVGAVQQAAAKKWAKPVGPEAKAQLDKNYAKVWQDLGAVDGTQYGVYFKAANKSLIWYNAAAFDNAGASEPKTWKDFLTTAETISASGVTPVSVGGADGWTLTDWFENVYLSQAGPEKYDQLAKHEIPWTDPSVKDALTTLAELFGKPELIAGGADGALQTEFPASVTQTFTGGDQPKGAMVFEGDFVAVNIAQTEAKIGTDAKVFPFPAVGADSPVVTGGDAAVALKDSKGAQALLTWLASADAAKIWAEAGGFISPNKGLDLKAYPNDVQRTMAQALIDAGDDVRFDMSDQAPQSFGGTPGAGEWKILQDFLKNPKDIAGTQKKLESEAVKAYKS
>NZ_CP010833.1|WP_075268514.1|5034691_5035978_-|sugar-ABC-transporter-permease
MTGTRRIVAAVFLLPALVLLGALVLYPIGYSVYRSFFDQAGTGFAGFDNYEALFTDDTIRTAVKNNAIWVVFAPTVATALGLIFAVLTERIRWGTAFKLIVFMPMAISMLAAGIIFRLVYDQAPERGVANAVAVSVHDTFNESAGFPKARPLPVHPLEKAAGGTFVSKEPIRAGEPLRVPLVGVAPAKMPGDARPAEGAPAASGDRISGTAWLDFTRGGGGKPNVVDPKELGLKGLKVEAVKDGKVVATATAGADGVFTLPASADGAQLRLPADNFREPYNGVDWLGPSLVTPGIIGSYVWMWAGFAMVLIAAGLAGLPRELLEAARVDGANEWQVFRRITVPMLAPVLAVVLVTLMINVLKVFDLVFIIAPGSSQDDANVLALQLYRSSFGTDADLGIGSAIAVLLLLLVIPVMLVNIRRIRKEGRR
>NZ_CP010833.1|WP_075266029.1|5033750_5034695_-|carbohydrate-ABC-transporter-permease
MSSAPDVNTARIGRQKAVTRKTGGTPEAPKAEQSLGARIAARAGGGVMRVFLVLVALFWLMPTIGLLLSSLRGPQDIAATGWWKIFTAPSELTFENYQRLLDNATITGSLGSTIMITVPSTVLVVLIGSFAGYAFAWMEFPGRDWLFLLVVGLLVVPVQVALIPVSELFGTIGIFETTLGVVLFHTAFGLPFAIFLLRNFFAEIPRELLEAARLDGAGEIRLFTRVVMPLGGPAIASLGIFQFLWVWNDMLVALIFADSESPPITVALQQQVRQFGNNIDVLAPGAFVSMVIPLAVFFAFQRQFVSGVMAGAVK
>NZ_CP010833.1|WP_075266028.1|5031314_5033546_-|bifunctional-glycosyltransferase-family-2-protein/CDP-glycerol:glycerophosphate-glycerophosphotransferase
MPRFSVIVPAFRVQAYLHACLDSVLAQSFKDYEIVVVDDCSPDACGPIADEYARRDPRVTALHLPRNIGLGPARNAGMGRAAGDYLIFLDGDDTLLPDALQTIADRIDATGEPDVLMYDYARTYWTGRSVRNVLAAHLDESGPERFRLTDRPELLRLLMVVWNKAYRRAFVEAEGFTFPPGYYEDTPWTYPVLMAADSIAVLDAVCVSYRQRRRGNILSTTSEKHFDVFDQYDRVFAFIDSRPELALWRPVIFRRMLDHFAALFASRDRLPLHSRAAFFRRATASCRRHHTPGAPAPRRALLRHGLMHLGARRTYRALSEAQRLGGRLRKGAAALRRAVRGAALRAHYRIQLRLPLRTRDAVFTTRAGSGYAGSPAAVEAKVRELVPGVRTAWVCRPADAHTVPTGTRHLAPGTFAHRTALARSAYLVNDGPFDRGLVKRRGQILLQTHEGTPLRTEGTDLLDRPAAARGTDFDELLRQVDTWDFSLSANPHSTLVRERAYPSAYTTLEYGSPRNDVYHRSDPADVARLRETLGIPEGATALLYAPVPRDYRRVQRPSLDLERLVRVLGPQFVILARVPRPAGPGVRGRAAHPRIIDVSAHRSVETLALASDALLTDYASLMFDYVNLDRPVVLHLDDIEAYEASRGTYFDITAFPPGVVARSQDELFDIFATDHWRGSRSAQLRAAFRARFCPYDDGYAAERVVRRVFLGETDGLPLPVPFPARRTPAALPAQDGAGAAVGG
>NZ_CP010833.1|WP_075266027.1|5030146_5031289_+|glycosyltransferase
MSRDIFIVSNSTDELGGVTGWMHQTARLFADQGHRVHTVGIHASDLKMTLPRQPDHPVTALYAAHPPTPWTPHGVRDRFRIPTRRKEAARVAAKRQAVGRLSELFATARPGAVVIVTQVWAMEWVGEADTTGLRVIGMSHESYDYSRASHRYRWIKNHYKDLDHWLVLTEEDADRWAGDGMNNVGFLPNALSRLPLVPSARTAKTVASIGRLSDQKGIDLLLDSWALVAPARPDWTLRVYGAGEDEAALKAQCTGLGLDGSVEWMGRTDDVERALAGSSVFVQSSRGEGFPLALLEAMASGVPCAAFDCAPGVREIVRDGEDGLLAPAGDVAALADRLLRLTGNPRLRDAMGARARSGVQRFSEPETLRRWEELFAFLER
>NZ_CP010833.1|WP_075266026.1|5027285_5030150_+|CDP-glycerol:glycerophosphate-glycerophosphotransferase
MSDVSCVITGGGDGEGPGGADALRASVESVLGQSMRAAEALVVLASAADPAVRTTARTLASRAPERVRLVHADPAARTTGALRNAGLDAATGRYVLVLGSGERLQKHACRNLWQAGETSRADLIAGRWSRTADESGKEREPSWQGELFARSRTLTRFTEAPQLVVRDALVTGFCLRREAARRHGLRYEEDLAHGEILFGPIAAASVGRIALVRRLIVTGRAVPDRARDLVALVEAHRRVANTLVARGLPELREEREQAFHRDHLVPLVRSFPALPAVRRDRVAAAAARTLTGPVPPDLPPLERVAVSLLGRGDAEGVLAAAYALSRPATVCAPLTTGADGRVGWGGEGEEPVADITELGHQYRRFGEMRLMNRLTRCAAADGGRLLLEGRLVLPGHTGPAPGAPLTATLEFRARGGARAVAFPAEVVRHDGTGITWRARADVVRRLRPVGVRDTAWDARLIVEADGARSVSDLFAPQDQVAGAVRFAARPRLGRLAGDTWEPYITLKDHFALRLAARRRPARTAHRLIRYATHFRPARKAKLLARALRKRLDRYRSRGFKAPAYNTWLIRLPVRRGSVVFESHMGTCYGDSPRALYEEIRRQGLKLHATWSYDPSPAGFPDDARLVRRWSWRYLWALARAEYWVDNQGFPPHLRKPRHTTYLQTWHGSAYKRMGFDETRVRLQNAPQRERLQQAVDRFDHFLVRSEHDVNTLARAYRLPEARLLRTGYPRNDALIAERTRAETEGRLPRPPLAGALGLDDHKKTVLYAPTFRGGPGKQRKSRLLLDVREFAERFGDTHTLLVRAHYLESARLPVCPPGTVVDVSRHHDVSELLAITDVLVTDYSSIMFDFALLDRPVVLFAPDLEAYAAERGSYFDLREQAPGPVTATQDELFAALAELKKSDTRYADQRRSFAERFGAYDQGDAARAAVAAVFGTAASRGVRHTTDHDRGAGR
>NZ_CP010833.1|WP_010070940.1|5047684_5047882_-|hypothetical-protein
MTYDRLVCANCAAPVSEGRCRVCRAVRQQMLEEQGQGPLAGMSPAMLIALMVVLLTALALLAQAA
>NZ_CP010833.1|WP_003968787.1|5048142_5048832_+|cell-division-ATP-binding-protein-FtsE
MIRFDNVSKTYPKQTRPALRDVSLDIEKGEFVFLVGSSGSGKSTFMRLILREERASTGMVHVLGKDLARLSNWKVPQMRRQLGTVFQDFRLLPNKTVAENVAFAQEVIGKPRGEIRKAVPQVLDLVGLGGKEERMPGELSGGEQQRVAIARAFVNRPMLLIADEPTGNLDPQTSVGIMKLLDRINRTGTTVIMATHDQNIVDQMRKRVIELEQGRLVRDQARGVYGYQH
>NZ_CP010833.1|WP_010062141.1|5048886_5049804_+|ABC-transporter-permease
MRAQFVLSEIGVGLRRNLTMTFAVVVSVALSLALFGGALLMREQVSTMKDYWYDKVNVSIFLCNKNDAKDMPKCAKGAVTKEQKAEIKADLEKMDAVETVHFETVDEAYKHYQEQFGDSPMAGNITPDQMQESFRVKLDDPQKYKVVATAFAGRDGVQSVQDQRSILDNLFELMNGMNVVAIYVMILMLVIALILIVNTVRVSAFSRRRETGIMRLVGASGFYIQAPFIMEAAVAGLIGGVLACAMLLGGRYFLIDGGLALQEKLNLINFIGWDAVLTKLPLVLAIGLLMPAVAALFALRKYLKV
>NZ_CP010833.1|WP_075266035.1|5049872_5051060_+|PDZ-domain-containing-protein
MSGFAQRFGPRGRRRGAALTLVFGCALATAAATGSLPQDPEPGPGPQTRAVSSTAAPVDHDEIEDAAAEAEADGKSVKDAAEEVVSRSGDRWGAVYDQREYEEFEQALDGTYTGVGLSARRTGRGDVTVSRVQPGGPADRAGIRTGDLLRTLDGRAIGKRPVAEVVALLRGDGTGAAEGSRVELGLVRKGRSWTETLERARLTTEAVTVRRLGDAPSSAVLVKVAAFTKGAGADVRDAVRDAPEGAGILLDLRANSGGLVAEAVVAASAFLDGGLVATYDVRGDQHALYADPGGDTDRPVVVLVDGGTMSAAELLTGALQDRGRAVTVGSPTFGKGSVQMPSRLPGGSVAELTVGHYRTPGGRNVDGRGITPDLVVGERAQQRAETVLSGLGGGS
>NZ_CP010833.1|WP_003968790.1|5051078_5051567_+|SsrA-binding-protein-SmpB
MAKEKDTGRKMIAQNKKARHDYTILDTYECGLVLMGTEVKSLRMGRASLVDGFVQIDDHEAWLHNIHVPEYVQGTWTNHAAKRKRKLLLHRAEIDKLESKSQETGHTIVPLALYFKDGRVKVEIALAKGKKEYDKRQTLREKQDTRETNRAIAAARRRQRSA
>NZ_CP010833.1|WP_159027441.1|5052126_5052291_-|hypothetical-protein
MLKSLVQWFNTADRAAGWVIETEEREDIGLVLEELAHVAGHPSLVMEADEWREW
>NZ_CP010833.1|WP_079181629.1|5053066_5054305_-|MFS-transporter
MVAAPRSAPTGSGRRRSRPSSNPYLRLLATPGARAFTAGNLIARLPMGMLSVSAVIMIAGSRGSYALAGAVTATGLAATAVVAPFTARLVDRFGQARVAVPATALAVLGSLALVLCVHHDAPAWTLFAAYAATATTPNTGGMSRARWAYLHRGDPAALHTANSFEQAADELCFMLGPVLAATLCGALFPEAGTLVGAVLLMTGVLIFAAQRATEPPVTPRTRAVASPLRTPGMPALLAVFLATGAVFGSLEVVSIAHAGGAILALQAAGSCAAGLLYGSLRPARNVHLRLLLCLAAMTALMSLPLLAATGSAALPVLALCLLLAGAATAPSMVTGMTLVQRATRPEQLNEGMTLSVTALLGGVAVGAAVGGRLVEHAGTAPGYVAPVSAAALALVIAAAGRRIPNRTSAQAC
>NZ_CP010833.1|WP_075266037.1|5054504_5055476_+|LysR-family-transcriptional-regulator
MPPADTDPRLLRAFLAVADELHFTRAAARLFVAQQALSRDIRRLERELGAELFVRTTRQVALTPDGERLLPYARRVLDAHSELAGAFSGAPARPLLVDLNSDGATAARVLGRARELVPECELMARFESGLTWAAAEILAGRLDASFGRAAGLAPAVRAGLSTHPVRYEPMALMLPLSHPLAERETVALAELSGETVYAGAGNERTREWTGLAASLFAEWDIVMAPPVPLAVGVAEFQRVMEKGGHPVLAVVDFPPMPGTVLRPLVDPVPLSPVSLVWRKGLRHPGVDALRNATDQLALAEGWLVRPSGAWLPESDLSLMRNRS
>NZ_CP010833.1|WP_075266038.1|5055638_5056334_+|hypothetical-protein
MDNWREGTRTGHTHEPNDATIQLDGLGRQLAELPGEPAPPDGSDGPVFVDESGRRSKTFRRLGWVLATVCAGYAVTLVFAVLGGNSSAPWLPLSGPKEEAKAEQVEDLPETGADTVDDGLSDDAPEPGPSASGSPAAGASGAPAGATPSATSVVVPAGSADRPSASASADPSRPATGGGGGGGGATKPAPTTPTAKPPVGPTPPTTEPEPTEPTAPPVVDPEQPVQEESAP
>NZ_CP010833.1|WP_075266039.1|5056334_5058551_+|glycosyltransferase
MNSPATRGRNGKDSRRRKASRGRSRLRLPMRYLLPTTLLVALLAMLMLRGYVHSEILADHRVRDAAPTHQVPEDVLTGGPVIDARSGDAKTLRIPDRRIVLTFDDGPDPVWTPKVLDKLKEYDAHGVFFVTGNMAARHPDLVRRMVEEGHELGLHTFNHPDLSYQSSARIDWELSQNQLALAGAAGIRTSIFRPPYSSFSDAMDNKSWPVTEYIGSRGYLTVVNDTDSEDWKRPGVHAIVERATPKNGKGAIILMHDSGGDRSQTVAALDTLLPDLKAKGYTFTRLTTALDAPSAHTPVTGFALWKGKAFVSAVAVSERITGVLVVGLAAIGALVLARFGLMLLLSFLHARKVRRRNFSWGEPLSRPVSVLVPAYNERECIEATVRSLAASEHPIEIIVIDDGSTDGTADLVEAMRLPRVRVVRQQNAGKPAALNNGIRHARYDIVVMMDGDTVFEPATVRELVQPFADPRVGAVAGNAKVGNRDSLIGAWQHIEYVMGFNLDRRMYDVLGCMPTIPGAVGAFRREALERVGGMSEDTLAEDTDITMALHRDGWRVVYAENARAWTEAPESVQQLWSQRYRWSYGTMQAIWKHRRAVIERGPSGRFGRVGLPFVSLFMVVAPLLAPLIDVFLLYGIVFGPTGKTVAAWFGVLVVQAVCAAYAFRLDKERMTHLLSLPLQQILYRQLMYVVLLQSWITALTGGRLRWQKLRRTGAVEAPGGVSAQRRGTGSAPERRPVG

Crispr_ID: NZ_CP010833_19

• CRISPR_ID: NZ_CP010833_19
• CRISPR_location: 5482261-5482355
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_19

Consensus_repeat	Method
CAGCGGGCCGCCGCTCGCCGATG	CRISPRCasFinder

spacers of NZ_CP010833_19

>19.1|5482284|49|NZ_CP010833|CRISPRCasFinder
TCTCCCTGCTCCTCGGCGAATCCTCGTTCGCCGACTCCGCGCCGCTGAC

CRISPR arrays and Neighbor proteins around NZ_CP010833_19

CRISPR arrays

The CRISPR arrays of NZ_CP010833_19

>merge|NZ_CP010833|19|5482261-5482355|CRISPRCasFinder
CAGCGGGCCGCCGCTCGCCGATGTCTCCCTGCTCCTCGGCGAATCCTCGTTCGCCGACTCCGCGCCGCTGACCAGCGAGCCGCCGCTCGCCGATG

>NZ_CP010833|19|17|5482261-5482355|CRISPRCasFinder
CAGCGGGCCGCCGCTCGCCGATG	TCTCCCTGCTCCTCGGCGAATCCTCGTTCGCCGACTCCGCGCCGCTGAC
CAGCGAGCCGCCGCTCGCCGATG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075266429.1|5476886_5477951_-|mechanosensitive-ion-channel-family-protein	unknown	unknown	gnl|CDD|223740
NZ_CP010833.1|WP_075266431.1|5482459_5484781_+|4-alpha-glucanotransferase	unknown	unknown	gnl|CDD|376788
NZ_CP010833.1|WP_075266432.1|5484819_5485032_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266436.1|5488073_5490656_-|aminopeptidase-N	unknown	unknown	gnl|CDD|274121
NZ_CP010833.1|WP_075266428.1|5475489_5476695_-|ROK-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224851
NZ_CP010833.1|WP_075266430.1|5478849_5481840_-|hyaluronidase	unknown	unknown	gnl|CDD|369423
NZ_CP010833.1|WP_075266426.1|5473140_5474082_-|sugar-ABC-transporter-permease	unknown	unknown	gnl|CDD|224096
NZ_CP010833.1|WP_075266422.1|5468254_5469640_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266437.1|5490781_5491282_+|DUF1203-domain-containing-protein	unknown	unknown	gnl|CDD|377693
NZ_CP010833.1|WP_075266439.1|5496197_5497274_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266425.1|5472225_5473137_-|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl|CDD|223472
NZ_CP010833.1|WP_075266434.1|5486127_5487282_+|allantoicase	unknown	unknown	gnl|CDD|237319
NZ_CP010833.1|WP_075266423.1|5469993_5470968_-|ATPase	unknown	unknown	gnl|CDD|225518
NZ_CP010833.1|WP_075266435.1|5487384_5487930_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266433.1|5485153_5486062_+|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|176115
NZ_CP010833.1|WP_075266438.1|5491355_5492384_-|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|237845
NZ_CP010833.1|WP_075266424.1|5470958_5472224_-|6-phospho-beta-glucosidase	unknown	unknown	gnl|CDD|133432
NZ_CP010833.1|WP_006124472.1|5478265_5478802_+|HNH-endonuclease	unknown	unknown	gnl|CDD|224321
NZ_CP010833.1|WP_075266427.1|5474089_5475421_-|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270451
NZ_CP010833.1|WP_075268549.1|5492640_5495943_-|S8-family-serine-peptidase	unknown	unknown	gnl|CDD|173796

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075266429.1|5476886_5477951_-|mechanosensitive-ion-channel-family-protein	gnl|CDD|223740	COG0668, MscS, Small-conductance mechanosensitive channel [Cell envelope biogenesis, outer membrane].	1.62723e-37
NZ_CP010833.1|WP_075266431.1|5482459_5484781_+|4-alpha-glucanotransferase	gnl|CDD|376788	pfam02446, Glyco_hydro_77, 4-alpha-glucanotransferase. These enzymes EC:2.4.1.25 transfer a segment of a (1,4)-alpha-D-glucan to a new 4-position in an acceptor, which may be glucose or (1,4)-alpha-D-glucan.	1.50213e-156
NZ_CP010833.1|WP_075266436.1|5488073_5490656_-|aminopeptidase-N	gnl|CDD|274121	TIGR02412, Aminopeptidase_N, aminopeptidase N, Streptomyces lividans type. This family is a subset of the members of the zinc metallopeptidase family M1 (pfam01433), with a single member characterized in Streptomyces lividans 66 and designated aminopeptidase N. The spectrum of activity may differ somewhat from the aminopeptidase N clade of E. coli and most other Proteobacteria, well separated phylogenetically within the M1 family. The M1 family also includes leukotriene A-4 hydrolase/aminopeptidase (with a bifunctional active site).	0
NZ_CP010833.1|WP_075266428.1|5475489_5476695_-|ROK-family-transcriptional-regulator	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	3.65936e-45
NZ_CP010833.1|WP_075266430.1|5478849_5481840_-|hyaluronidase	gnl|CDD|369423	pfam07555, NAGidase, beta-N-acetylglucosaminidase. This family has previously been described as a hyaluronidase. However, more recently it has been shown that this family has beta-N-acetylglucosaminidase activity.	8.32236e-141
NZ_CP010833.1|WP_075266426.1|5473140_5474082_-|sugar-ABC-transporter-permease	gnl|CDD|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.98423e-71
NZ_CP010833.1|WP_075266423.1|5469993_5470968_-|ATPase	gnl|CDD|225518	COG2971, COG2971, Predicted N-acetylglucosamine kinase [Carbohydrate transport and metabolism].	2.34194e-23
NZ_CP010833.1|WP_075266427.1|5474089_5475421_-|ABC-transporter-substrate-binding-protein	gnl|CDD|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.18072e-78
NZ_CP010833.1|WP_075266425.1|5472225_5473137_-|carbohydrate-ABC-transporter-permease	gnl|CDD|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.12932e-82
NZ_CP010833.1|WP_075266434.1|5486127_5487282_+|allantoicase	gnl|CDD|237319	PRK13257, PRK13257, allantoicase; Provisional.	1.50923e-171
NZ_CP010833.1|WP_075266437.1|5490781_5491282_+|DUF1203-domain-containing-protein	gnl|CDD|377693	pfam06718, DUF1203, Protein of unknown function (DUF1203). This family consists of several hypothetical bacterial proteins of around 155 residues in length. Family members are present in Rhizobium, Agrobacterium and Streptomyces species.	1.02792e-42
NZ_CP010833.1|WP_075266438.1|5491355_5492384_-|aspartate-semialdehyde-dehydrogenase	gnl|CDD|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	0
NZ_CP010833.1|WP_075266424.1|5470958_5472224_-|6-phospho-beta-glucosidase	gnl|CDD|133432	cd05296, GH4_P_beta_glucosidase, Glycoside Hydrolases Family 4; Phospho-beta-glucosidase. Some bacteria simultaneously translocate and phosphorylate disaccharides via the phosphoenolpyruvate-dependent phosphotransferase system (PEP-PTS). After translocation, these phospho-disaccharides may be hydrolyzed by the GH4 glycoside hydrolases such as the phospho-beta-glucosidases. Other organisms (such as archaea and Thermotoga maritima ) lack the PEP-PTS system, but have several enzymes normally associated with the PEP-PTS operon. The 6-phospho-beta-glucosidase from Thermotoga maritima hydrolylzes cellobiose 6-phosphate (6P) into glucose-6P and glucose, in an NAD+ and Mn2+ dependent fashion. The Escherichia coli 6-phospho-beta-glucosidase (also called celF) hydrolyzes a variety of phospho-beta-glucosides including cellobiose-6P, salicin-6P, arbutin-6P, and gentobiose-6P. Phospho-beta-glucosidases are part of the NAD(P)-binding Rossmann fold superfamily, which includes a wide variety of protein families including the NAD(P)-binding domains of alcohol dehydrogenases, tyrosine-dependent oxidoreductases, glyceraldehyde-3-phosphate dehydrogenases, formate/glycerate dehydrogenases, siroheme synthases, 6-phosphogluconate dehydrogenases, aminoacid dehydrogenases, repressor rex, and NAD-binding potassium channel domains, among others.	0
NZ_CP010833.1|WP_006124472.1|5478265_5478802_+|HNH-endonuclease	gnl|CDD|224321	COG1403, McrA, Restriction endonuclease [Defense mechanisms].	1.08573e-20
NZ_CP010833.1|WP_075266433.1|5485153_5486062_+|LysR-family-transcriptional-regulator	gnl|CDD|176115	cd08423, PBP2_LTTR_like_6, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator, contains the type 2 periplasmic binding fold. LysR-transcriptional regulators comprise the largest family of prokaryotic transcription factor. Homologs of some of LTTRs with similar domain organizations are also found in the archaea and eukaryotic organisms. The LTTRs are composed of two functional domains joined by a linker helix involved in oligomerization: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal substrate-binding domain, which is structurally homologous to the type 2 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcriptional repressor undergoes a conformational change upon substrate binding which in turn changes the DNA binding affinity of the repressor. The genes controlled by the LTTRs have diverse functional roles including amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to a name a few. This substrate-binding domain shows significant homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.43571e-45
NZ_CP010833.1|WP_075268549.1|5492640_5495943_-|S8-family-serine-peptidase	gnl|CDD|173796	cd04857, Peptidases_S8_Tripeptidyl_Aminopeptidase_II, Peptidase S8 family domain in Tripeptidyl aminopeptidases_II. Tripeptidyl aminopeptidases II are member of the peptidase S8 or Subtilase family. Subtilases, or subtilisin-like serine proteases, have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure (an example of convergent evolution). Tripeptidyl aminopeptidase II removes tripeptides from the free N terminus of oligopeptides as well as having endoproteolytic activity. Some tripeptidyl aminopeptidases have been shown to cleave tripeptides and small peptides, e.g. angiotensin II and glucagon, while others are believed to be involved in MHC I processing.	5.0527e-59

Protein sequences

>NZ_CP010833.1|WP_075266430.1|5478849_5481840_-|hyaluronidase
MRIGRRRQATAVAAAVIGGLLGSVSVAPSAAAAPGDPGRPVTDTADRADSARTPSVWPRPQSMKTTGSAVPLGSEATLVAAPDADPYAVEQTRSLLRSAGVRTLHESLPGRGPVVRLGGTGAGEALRALRAPDRADLPSGGYRLAVGEAAGRATVALEGLGGDGLFHAVQTLRQLTVGGSVAGVTVRDWPGTAVRGMAEGFYGQPWTRDERLAQISFMGRTKQNRYLYAAGDDPYRLARWREPYPADQRADFRALAERARAEHVTLGWALSPGQAMCMASDQDVRALTKKADAMWALGVRVFQLQFQDVSYSEWHCDLDSETFGSGPKAAARAQARVAGALARHLAERYPDAAPLSVLPTEFYQDGATDYRTALAAELDDRVQVAWTGVGVVPKKITGGELAGARAAFRHPLVTMDNYPVNDYAQDRIFLGPYTGRDPAVASGSAALLANAMEQPSASRIPLFTAADFAWNPKGYDPAASWRAAIDDLAGGDASARDALLALAGNSAGSVLGAEESAYLRPLLDAFWSTRADASRRDRAADTLRAAFSVMRQAPERLKTPAEGRLTDEVRPWTEQLARYGRAGELAVDLLQAQAAGDGAAAWRIQLALEPLREEIGAGRATVGKGVLDPFLDKAAKVAAGWNGTDRASGRVTKDAGGYTVRLDAPRPVEAVTALAEPGHALADAVVEAHVPGEGWRPLGRLSPSGFTQTEAKGLRADAVRVTVPEAAGNARPPYLSPTLPAAPAVVAGTPQVRALVPWFGDEPAATLDLKHGETDAEIGGEPQRVAARLAGRRPAEVRGKLTAKAPKGIEVRVPKQTTVPRGSRTEVPVDITVPKDTPAGEYEVPLTFGGQESTLTVRAFPRTGGPDLARTAKASSSGDETPDFPASAATDGDPETRWSSPVEDGAWWQTELEKPVRLGQVVLSWQDAYASRYRIQVSADGRVWRTAATVTEGRGGRESVRMDAKDTRFVRVQGERRATEYGYSLWSVEAYAVADD
>NZ_CP010833.1|WP_006124472.1|5478265_5478802_+|HNH-endonuclease
MPHVLVLNASYEPLGVVPLRRALVLVLENKAICLEESGAFLHSATRAVPAPSVVRLKRFVRVPYRGPVPLTRRALFARDGGRCMYCGAAATSVDHVIPRSRGGQHAWDNVVAACRRCNHVKADRHLPELGWRLRHQPAPPTGLAWRIIGTGHRDPRWLPYLQPFGADDVMARIDGVSA
>NZ_CP010833.1|WP_075266429.1|5476886_5477951_-|mechanosensitive-ion-channel-family-protein
MSLSVLLAAAPSPEPVGSLGEAAEQAGNAAGWVEENWSTWLSTGLRILLIVAVAITLRYLIRRALTNLIDRMNRSAQAVEGTALGGLLVNAERRRQRSEAIGSVLRSVASFLIMGTAALMILGAFKINLAPLLASAGVAGVALGFGARNLVTDFLSGVFMILEDQYGVGDTIDAGVASGEVIEVGLRVTKLRGDNGEIWYVRNGEVKRIGNLSQGWSTAGVDVTVRPTEDLEQVRKAITAAAESMTKEEPWSERLWGPVEVLGLDAVLLDSMTVRVTAKTMPGKSVGVERELRWRIKQALDDAGIRMIGAVPLQQDESAADPTAGVAAPSAYASATSPQSMATTPIPPTSLNKH
>NZ_CP010833.1|WP_075266428.1|5475489_5476695_-|ROK-family-transcriptional-regulator
MTGTTPGTPRVLRAMNDRAALDLLLEHGPLSRTRIGKLTGLSKPTASQLLARLEAAGLVVATGTSEGRPGPSAQLYTVNPRAAHVAGLDVNGQRIVAAVADVTGATVGQFELATPGRRADSVVRQVADALDGAVKEAGLTRADVHRIVIGTPGAFDPGTGRLRYASHLPGWHSPTLLDELAAFLPMPVEYENDVNLVAVAEQRLGAARGHEDFVLLWNEEGLGAALVINGRLHRGFTGGAGEVGFLPVPGTPLVRQVVKANSGGFQELAGAQAVPRLAKALGIDTPQQPYAKVAAELLARAAAAYEEDEALTELLRQYAQRLATGLASVTAVLDPGLIVLSGGAVAAGGEILRSLIQSELAELAASRPRLVVGEIDRTPVLRGALERALADTRDEVFDTSR
>NZ_CP010833.1|WP_075266427.1|5474089_5475421_-|ABC-transporter-substrate-binding-protein
MRTSRLTTTAVAVAAISVLATACTGQSEAGASDDPDAKTTINFWHGWSAPAEVKAVQDNIDRFEKAHPNITVKVSGNINDDKLNQALRAGGSDGPDVVSSFTTANVGKFCSSGAFTDLQPFIEKSKLDLEKTFPKVLQDYTQFEGKRCALPLLTDAYGLYYNKDAFEKAGITAPPKTMSELADVAKKLTVEKGDTYQQLGFMPNFHGYETVVSHYMPSWEHAYFDENGKSNIAKDPAFAKMFTYQKKLVDSLGGYSKLEKYRGTFGDEWGAKHPFHTGQVAMQLDGEWRLGMAEDAGADFEIGVAPMPVADDEADSYGKGYLSGTIVGIAPASKKQNAAWELVKFMTTDTEAVVNFSNGIRNVPSTLEALKSPDLKFDPRFKTFLDIAQHPESSTSDGAVNGATYQLTLQDFGYQYEKGAVKDLQAGLEKTAKQIDTDIAKAK
>NZ_CP010833.1|WP_075266426.1|5473140_5474082_-|sugar-ABC-transporter-permease
MTTHTLRSKRRRSALRNAAFMSPWLIGFSVFFAYPMVSTVYFSFTSYDGFGAPAFNGLTNWTYVFRDYPMFWPSLWNTLWLVLVVVTCRVVFGLGIGLLITKIKTGTGVFRTLFYLPYLAPPVAATLAFVFLLNPGTGPVNAILGDFGLPTPGWFNDASWSKPALTMLAVWGIGDLMVIFMASLLDVPTEQYEAAELDGASAWQKFRFVTLPNISPIVLFAVVTGVIQAMQYYTQPLVAGKVASGVIGGSGQSFEPGYPDKSTLTLPQLVYNLGFQRFDYGAACVVALVLFALAMAFTALLMRGRNNLISAGD
>NZ_CP010833.1|WP_075266425.1|5472225_5473137_-|carbohydrate-ABC-transporter-permease
MTDLLDPVRKAATASPERPSRTPAARTARRKALLHWIAVHSLGIAAALFFVLPFVFVVLTSLMSDQQALTRDLTPNTWEWGNYERVFNTPGFLTWWRNTLLYAGVGTVLTVVSSIPVAYALAKFRFRGRKLSLMLVISMMMLPPQVVIIPMYLFWAKQMDLSGTLWPLIIPMAFGDAFSIFLLRQFLLTIPNEYLDAAKVDGCGEFRTLMKVVLPMARPGIAAIALFQFFAAWNDYFGPQIYASENPAAWTLSYGLESFKGAHHTDWNLTMAATVLVMAPVIAVFFFAQKAFVEGVTLTGVKG
>NZ_CP010833.1|WP_075266424.1|5470958_5472224_-|6-phospho-beta-glucosidase
MKLAVVGGGSTYTPELIDGFARLRDTLPIEELVLVDPAADRLELVSGLARRIFAKQDHAGKITTTTDIDAGVADADAVLLQLRVGGQAARNQDETWPLECGCVGQETTGAGGLAKALRTVPVVLDIAERVRRTNPDAWIIDFTNPVGIVTRALLQAGHKAVGLCNVAIGFQRKFARLLEVEPGQVHLDHVGLNHLSWELGVRLGGPDGENVLPKLLAEHGDAIADDLHMPRKLVDRLGVVPSYYLRYFYAHDEVVKELGTKPSRAAEVAAMEKELLEMYGDPALDEKPELLARRGGAFYSEAAVDLAASLLGDGGSPVQVVNTYNNGTLPFLADDAVIEVQARVGRDGATPLAVPALDPLYAGLIANVTAYEDLALEAALRGGRDRVFKALLAHPLIGQYDYAEGLTDRLIAHNREHLAWA
>NZ_CP010833.1|WP_075266423.1|5469993_5470968_-|ATPase
MGVNVSVVAIDAGNSKTDVALIGEDGTVLATARGGGFQPPAIGVEAAIDVLAGVLERAVAELPAPPVLSGHVSACLANADLPVEEAELAAALETRGWGSSVEVRNDTFAILRAGVDEPRGVAVVCGAGINCVGMTPDGRTARFPAIGRISGDWGGGSGLAEEALWFAARAEDGRGEASELARTLPRHFGLDSMYGLIEALHRGAIPLGRRHELTPVLFATAEAGDPVAAALVKRQAHEVVAMASVALDRLDLLEEEVPVLLGGSVLAARHPQLNDRIAALLAARAPKAEVRVVSEPPVLGAALLGLDRTGAGPEAHRKLRARYA
>NZ_CP010833.1|WP_075266422.1|5468254_5469640_-|hypothetical-protein
MTHPPSGGSQTSRTPDPASGHVGVPEQRTTWTTQARRLRAVATTEPGRLQIIGAVLALLVVAFGAVTTLEISQRASSADDVVSRSQPLSADAADIYRFLADADTTAASGFLAGAQEPEAVQEQYRKDIEEAARLLVKASGSTDSASASSREIATLNKLLPVYTGLIERARANNRQGLPLGGAYLRYANQKMTGEMLPAAERLYAAETGRLESDSADARQWPLWSIGAGIVVLGALGWMQRRTYRRTNRMLNPGLLAATAAASVVVLWLAVGHTVARAELRSAMVHGQESLDVLNDARINSLKARANENLTLVARGAVLTPDGSADQYEADYSSGMAALKAQLKKAGRLADDAGGSAPVAEAADGVSQWQVRHREARATDDRGDYDGALEQIIGTEKSTGQSFQQVDAALEKALAHEQGEFTSAAKDGRGALRGLPAGAAALAVLGAVAVIAGVNRRLSEYR
>NZ_CP010833.1|WP_075266431.1|5482459_5484781_+|4-alpha-glucanotransferase
MGLSRLAALHGVATSYSPSPDVTVSVPDDTVIAVLAALGVDAGTPADVRKCLAAAESRSRLLPPTVVVWAGESLPSALAGLPPGSTVTVEPEPSDPPGHPAGRPPAPLSMRARAASPATGARAEAAPASGAPAGSPAPGAPVGFPAADASGTAPAEAAETAGGAVPPRGDEAAGAPAAAPAPPAWWIPPPHGVHRIHVRTPDNRRATATLVAAPPRVPQPPERTHGFLVQLYSLLSARSWGMGDLGDLTDLATWAGRSVGSGFVQVNPLHAAVPGKPTDPSPYRPSSRRFPDPVHLHVESIPEYGHVRDRATLDDLRQDAAALSEAVLNKGALIDRDAVWELKRQALELVVRVPLTPGRRADYCDFLAEQGQALEDHALWCALAEVHGPDWHTWPEALRDPRSVGTARARSELLDRVDFHCRLAWLTAGQLAAAQRAAEDAGMGVGIVHDLAVGVHPAGADTWSQQEAFAHGMSVGAPPDAFNARGQDWGLPPWRPDTLAATGYAAYRGLLRGLLAHAGALRIDHVMGLFRLWWVPEGRPPTDGTYVAYDAEAMLAVLVLEAHRARTAVVGEDLGTVAPGVREALARRGVLGTSVLWFERDWEGDGRPLAPEKWRRDCLATATTHDLPSTAARLTGDHVTLRHRLGLLTRSLEEELTEDATGTAEWLALLARLRMLPEGDGDEEAAVRAVHRFLRRTPARMTGVWLPDTVGDRRPQNLPGTWDQYPNWRLPIADPEGHPVTLEEITASPRLHALMEVLRPRKPRTAPPGERRP
>NZ_CP010833.1|WP_075266432.1|5484819_5485032_+|hypothetical-protein
MRAGVVAAGTTLMMLLMSAPALALTPDDGDDPAPRLSAIETIGLYVVAPIALFVVITVLVMVLDKSKKQV
>NZ_CP010833.1|WP_075266433.1|5485153_5486062_+|LysR-family-transcriptional-regulator
MTEWDVKKLRILRTLRDRGTVTATAEALLMTPSAVSQQLTNLARQLGVDLLEAQGRRVRLTDAAHLVLRHAEAVFAQLERAEAELTGYLRGEAGEVRVAAFSTAVPALVVPAVRLLRAEDRPGPDVRVREAEAAQAYELLTAGEVDLALSLAAHAPTARDPRFSLFPLLADPLDVALPADHPLADAPGLRLADLAADRWIFGGSGPWSEITTAACEAAGFVPEQAHSAAGWTAILALVEAGMGVALVPRMAARERREDVVMRVLEADRPRRHVVAALRHGAESGPAVARVLAALTETARSFS
>NZ_CP010833.1|WP_075266434.1|5486127_5487282_+|allantoicase
MTFDASETTFQNSDTDPHANDAAPYGGGDPYADYREAGDLPFTELVDLADRRLGAGVIAANDEFFAERENLLIRERAVFDPEHFGHKGKIMDGWETRRRRGADADHPFPAPEDHDWAIVRLGAPGIVRGLVVDTAHFRGNYPQRVSVQATSVEGAPGPEQLLADDVKWEEILPPTPVRGHAANAFEITSGRRYTHIRLCQHPDGGIARLRVHGEVVPDPAWLAALGTVDLISVLNGGTYEDASDRFYSSPTQIILPGTSRKMDDGWENRRRRVRDTNDWVRFRLPAQGAVRAIEIDTAYLKGNSAGWIALQGRNGDTGEWFEILPRTRLQPDTLHRFVLRAQAVVTHVRLDAFPDGGVARMRLHGTLTESGAAELTRRYEESGA
>NZ_CP010833.1|WP_075266435.1|5487384_5487930_-|hypothetical-protein
MPGFAAAVPVALALCAGLMTGPSPAPAAVASATDCRAGPAGCYDLYTYGYSLGLHPFTEPDAVRRQLTDHFWLFPVSGGCAGRIRAGARCELLGGNPVEVEYIGDDFFQINTLPGHQLGRGMHIRFAFSRTLGFHTMTVRAWQDRPTDCTGETFCNGVNRAFAWVTWRVLAKTLRFTAYAA
>NZ_CP010833.1|WP_075266436.1|5488073_5490656_-|aminopeptidase-N
MPGTNLTREEAQERARLLTVDAYEIDLDLSGAQEGGTYRSVTTVRFDSAEAGAETFIDLVAPAVHEAVLNGAALDVAAVFHDSRIALAGLREGANELKVVADCSYTNTGEGLHRFVDPVDEQAYLYTQFEVPDARRVFASFEQPDLKATFRFTVKAPSGWTVISNSPTPEPKDDVWSFEPTPRISTYITALIVGPYHSVHSTYEKDGQTVPLGIYCRPSLAEYLDADDIFAVTRQGFAWFQEKFDYAYPFAKYDQLFVPEFNAGAMENAGAVTIRDQYVFRSKVTDAAYEVRAETILHELAHMWFGDLVTMEWWNDLWLNESFATYTSIACQADAAGSKWPHSWTTFANSMKTWAYRQDQLPSTHPIMADISDLDDVLVNFDGITYAKGASVLKQLVAYVGKDAFFQGVQAYFKAHAFGNTRLSDLLGALEKTSGRDLKTWSKAWLETAGINILRPEIETDENGVVTSFTVLQEAPALPAGAKGEPTLRPHRIAIGCYSIDDAADGKLVRTDRIELDVDGERTDVPALVGKARPAVVLLNDDDLSYAKVRLDAESLRVVTEHLGDFAESLPRALSWASAWDMTRDGELATRDYLSLVLSGIGKESDIGVVQSLHRQVKLALDLYAAPETRQAALNQWTEATLAHLQTAEPGSDHQLAWARAFAATARNPQQLDLLQSLLDGTESIEGLAVDTELRWAFVQRLAAAGLLDEEEIAAEYERDKTAAGERHAASARAAQPSEEAKAQAWAAVVDSGELPNSLQEAVISGFVQPDQRELLAPYTEKYFASVKEVSDSRSHEMAQQIIVGLYPALQVSQETLDATDAWLASAEPSAALRRLMSESRSGVERALKAQAADAAAATA
>NZ_CP010833.1|WP_075266437.1|5490781_5491282_+|DUF1203-domain-containing-protein
MTGYEPRPIDPAALGELRATDDAGRPCRPFTADEGGHPLRCCLRGSEPGERIALVSYAPLRRWAAATGASPGAYDEQGPVFLHAEACAGPDPEREGYPFSRPGALRTVRRYDAHGRIVGGRLLEIPAEEAKGFDAALDEAFADPEVVLVHVRAVEYGCFHFEVRGN
>NZ_CP010833.1|WP_075266438.1|5491355_5492384_-|aspartate-semialdehyde-dehydrogenase
MKVGIVGATGQVGTVMLRILAERSFPVDELRLFASARSAGSTIDFQGSPVTVEDASTADYTGLDIVLFSAGGATSKALAEKVAAQGAVVIDNSSAWRKDPEVPLVVSEVNPHAAKVRPKGIIANPNCTTMAAMPVLRPLHDEAGLEALTVATYQAVSGSGLAGVSELHGQASKVVADAEKLVHDGEAVDFPEPGVYERPIAFNVLPLAGSIVDDGSFETDEEQKLRNESRKILEIPELKVSGTCVRVPVFSGHSLQINARFARPIGVERAYELLKDAEGVELSEIPTPLQAAGKDASYVGRIRVDETVDHGLALFVSNDNLRKGAALNAVQIAELVAAELKG
>NZ_CP010833.1|WP_075268549.1|5492640_5495943_-|S8-family-serine-peptidase
MTKESPSSIPGARRAARIAAAAGLVAALTATGAAPVFAVGDPAPAPVKPAATSDRGDKLGKADADVLAKAEAKGEKNITMMVATTPGATEQVSKQLDAVEGSVLGKTYDKLGYVRATVPTKSAESTIKAASKLSSVLGIDLKQEIKLDDPTPKGDRAAGAKQTKATGSYAAPNKKTPAKNPYNPSFETGAVDFVAKNPKADGRGITIGILDSGVDLGHPALKKTTTGERKIVDWVTATDPVSDGDGTWLRMSESVSGPTFTAGGKTYTAPAGSYKFATFAESATTGGDMAGDLNRDGDTTDVWGVLYDPVTGTTRVDLNSNADFSDDKVLKPYKEKFQVSYFGEDDPRTPVVERIPFVVETRKGVTYNAAGAKADFVNIGVIEGSHGTHVAGITAANGLFGGEMNGAAPGAKIVSSRACTWSGGCTNIALTEGMIDLVVNRGVDIVNMSIGGLPPLNDGNNARAELYKRLVDIYGVQLVISAGNSGPGLNTIGDPALADHVISVGASISKETWAANYGSNVTKKYDMLPFSSRGPREDGGFTPILSAPGASINTTQTWAPGGPVKEAGYDLPAGYSMLQGTSMASPQAAGAAALLLSKAKQKGIELPPADLRVALTSTAGHIKDVPAHVQGSGLIDIVKAWKQIAKQGKPAHEFSVKAPVDTAIDFALKDPGFGTGLYDREGGLKVGETKVYDVVVTRTTGPDRDVQHKLTWKNNDGTFELSSPQYVSLPLDTPVKVKVKAKAKTAGVHSAILQVDDKKTSGVDHQIMTTVVIAQELQQPGYAYKASGSVQRNGTTSYFVNVPEGAKTLEVALSALRSGSQTRFIALHPYGTPVDPTSTVNCYPNYENPANTCRPDVRSYKDPQPGVWEIEVESRRTSPLLDNPYKLDVSLLGAAFDPAVRTIAEAKIGAPAAVDWKVTNTAAALQGKLQGGSLGSAKVDKPSISTGQTRETTVTIGAGVEKLDFAIGGTSDANADLDLYVFRGATQVGSGTTAGSEEAVSLLKPAAGTYTVIVDGYSVPSGSTTYDYRDVYYAASLGTIKVDSSKAVNLANGASAQVGAEVVVAGAAPEGRQFFGEVQLVNARGTAAGTGSVVIEKVTP
>NZ_CP010833.1|WP_075266439.1|5496197_5497274_-|hypothetical-protein
MTQNTPLSARLPRLPLHPGDVTQRVLSAAQLRARGVSAAQTSAQCLPGGPWQPLLPGVYLLHPGPPTGQERLRGALLYAGRPPVSARRTAAGPADAGYGEAMVTGVAALALHGFASVAELGALHRIDVLVPRTRRLRSTRFVEVLRTASMPGPVRVGEVPVAPVERALADAVAATADAADVRRLLTEAVRDGHCEPAAVVRELSEAKLLGRPAVVNAVDALLAEGRAVAEARLYAMVREHGLPDPVWNVELRLPGGPDLGGIDAYWPDHAVAVELDSRAPRHAVHGVPGRRSGRGKEDPQWSAYAAKREHLERLGITVVHLTPRKLREALDQQATVVRTALMAAADREPAAYVMVLPR

Crispr_ID: NZ_CP010833_20

• CRISPR_ID: NZ_CP010833_20
• CRISPR_location: 5739018-5741065
• CRISPR_type: TypeI-E
• Repeat_type: NA
• Spacer_info: 33 spacers
• Cas_protein_info: cas2,cas1,cas6e,cas5,cas7,cse2gr11,cas8e,cas3

Consensus repeat of NZ_CP010833_20

Consensus_repeat	Method
AGAGTGGACCCCGCGCCTGCGGGGATGGTCCGCCAGACCGG	PILER-CR
GTGGACCCCGCGCCTGCGGGGATGGTCC	CRISPRCasFinder
GTGGACCCCGCGCCTGCGGGGATGGTCCG	CRT
GTGGACCCCGCGCCTGCGGGGATGGTCC	PILER-CR

spacers of NZ_CP010833_20

>20.1|5739059|20|NZ_CP010833|PILER-CR
GCCCGCGCCAAGGCCCGGAG
>20.2|5739120|25|NZ_CP010833|PILER-CR
CCGGGAGAGACCACTGGGGGCCGTC
>20.3|5739049|33|NZ_CP010833|CRISPRCasFinder
GCAGGACCGGGCCCGCGCCAAGGCCCGGAGGAA
>20.4|5739110|33|NZ_CP010833|CRISPRCasFinder
CCCAGCCGGGAGAGACCACTGGGGGCCGTCAGA
>20.5|5739171|33|NZ_CP010833|CRISPRCasFinder
GCCTGACCGGCGCCCTCGTCGCGCCCCGCCTAG
>20.6|5739232|33|NZ_CP010833|CRISPRCasFinder
AGTCCGACCCGGGCCAGCTGAAAGGGAGCGAGG
>20.7|5739293|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
TCCGCAGTACGTCCAGTGCTCCGCGTGCAGGAC
>20.8|5739354|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GGCCGGTTTGTCGCTGATCCACCGGTAGACCAG
>20.9|5739415|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GAGCGAGGAGAAGCGCCTCGCGGAGCACCGAGC
>20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GGACTGCGCCGACCGCAACACCCCGCCCCCGGC
>20.11|5739537|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GCCCTTCACGCTGTACGGGGGGAGCGGGAGCGG
>20.12|5739598|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GTACCGGGGCGTCGCCCGCCTGTACTCCTCGCA
>20.13|5739659|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
CTGTCGGAGACGCAGCCCGGCAGCTGCTCGATG
>20.14|5739720|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GTTCACGGGTGACGCGCGGCGACTGTTCTTCGG
>20.15|5739781|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GGCATTGCCGTACCTACCGCTTGGCGGGCGTGA
>20.16|5739842|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GGTCTTTCTGACCTGGGGCGTTTCGGTTTCTCC
>20.17|5739903|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GGCCAAGGTCCGGGAGTGGGCGGCCACCCTCGG
>20.18|5739964|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GAGGCTAGACCCGGCCACGGTGGAGGCCGCCCG
>20.19|5740025|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GCCCAGCGCGGCCGAGCCCAGTCCGGCCCGCAG
>20.20|5740086|34|NZ_CP010833|CRISPRCasFinder,PILER-CR
GCGGTCCGGGGTTCACCTGATCACCCCCGCCCCC
>20.21|5740148|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
CCCGCAGCAGGTCGTCGACTGGATTCAGGCGCA
>20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GTCGGTGATCGGCCACCTGGAGTGGCAGCCGGG
>20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GGTCAGCCGCATCAGCGGCCTGCAACTGGGCGG
>20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GTGCTCCGCTTCCAGGTCGATGTCGGCGGCGAG
>20.25|5740392|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GGGGTTCGCATACCGGCTGCGCGGGCCGACGTA
>20.26|5740453|38|NZ_CP010833|CRISPRCasFinder,PILER-CR
GATTTGATCGGCACCGTCGGATGCACCGGCAACTCCTC
>20.27|5740519|33|NZ_CP010833|CRISPRCasFinder,PILER-CR
GCAGGTGATGGGCTCCATCAACTTGTTCGGGGT
>20.28|5740580|33|NZ_CP010833|CRISPRCasFinder
GTTCGTCTGCGACCGGTGCCATCGCGACATGCG
>20.29|5740641|33|NZ_CP010833|CRISPRCasFinder
GTCCGCCATTCCCGGACCGATTGCCGATGCCCT
>20.30|5740702|33|NZ_CP010833|CRISPRCasFinder
GATTGCGGCCGAGCTCGGCGTCACCTTCGGTGA
>20.31|5740763|33|NZ_CP010833|CRISPRCasFinder
GTCGGTACTCGGGTGACTCCGGTCGACCACGGT
>20.32|5740824|31|NZ_CP010833|CRISPRCasFinder
GACGAGGTGAACGTGGGCGTCGATGAGCCCT
>20.33|5740883|33|NZ_CP010833|CRISPRCasFinder
GAGGATCGGGATCACGGCGTGCATTCCTACGCC
>20.34|5740944|32|NZ_CP010833|CRISPRCasFinder
GGCAACGACGTCGTCGTGCCCTGCCAGACGAC
>20.35|5741004|33|NZ_CP010833|CRISPRCasFinder
GGCTGTCTGGACGGAACTCGACTCCCCCAGGGA
>20.36|5739050|32|NZ_CP010833|CRT
CAGGACCGGGCCCGCGCCAAGGCCCGGAGGAA
>20.37|5739111|32|NZ_CP010833|CRT
CCAGCCGGGAGAGACCACTGGGGGCCGTCAGA
>20.38|5739172|32|NZ_CP010833|CRT
CCTGACCGGCGCCCTCGTCGCGCCCCGCCTAG
>20.39|5739233|32|NZ_CP010833|CRT
GTCCGACCCGGGCCAGCTGAAAGGGAGCGAGG
>20.40|5739294|32|NZ_CP010833|CRT
CCGCAGTACGTCCAGTGCTCCGCGTGCAGGAC
>20.41|5739355|32|NZ_CP010833|CRT
GCCGGTTTGTCGCTGATCCACCGGTAGACCAG
>20.42|5739416|32|NZ_CP010833|CRT
AGCGAGGAGAAGCGCCTCGCGGAGCACCGAGC
>20.43|5739477|32|NZ_CP010833|CRT
GACTGCGCCGACCGCAACACCCCGCCCCCGGC
>20.44|5739538|32|NZ_CP010833|CRT
CCCTTCACGCTGTACGGGGGGAGCGGGAGCGG
>20.45|5739599|32|NZ_CP010833|CRT
TACCGGGGCGTCGCCCGCCTGTACTCCTCGCA
>20.46|5739660|32|NZ_CP010833|CRT
TGTCGGAGACGCAGCCCGGCAGCTGCTCGATG
>20.47|5739721|32|NZ_CP010833|CRT
TTCACGGGTGACGCGCGGCGACTGTTCTTCGG
>20.48|5739782|32|NZ_CP010833|CRT
GCATTGCCGTACCTACCGCTTGGCGGGCGTGA
>20.49|5739843|32|NZ_CP010833|CRT
GTCTTTCTGACCTGGGGCGTTTCGGTTTCTCC
>20.50|5739904|32|NZ_CP010833|CRT
GCCAAGGTCCGGGAGTGGGCGGCCACCCTCGG
>20.51|5739965|32|NZ_CP010833|CRT
AGGCTAGACCCGGCCACGGTGGAGGCCGCCCG
>20.52|5740026|32|NZ_CP010833|CRT
CCCAGCGCGGCCGAGCCCAGTCCGGCCCGCAG
>20.53|5740087|33|NZ_CP010833|CRT
CGGTCCGGGGTTCACCTGATCACCCCCGCCCCC
>20.54|5740149|32|NZ_CP010833|CRT
CCGCAGCAGGTCGTCGACTGGATTCAGGCGCA
>20.55|5740210|32|NZ_CP010833|CRT
TCGGTGATCGGCCACCTGGAGTGGCAGCCGGG
>20.56|5740271|32|NZ_CP010833|CRT
GTCAGCCGCATCAGCGGCCTGCAACTGGGCGG
>20.57|5740332|32|NZ_CP010833|CRT
TGCTCCGCTTCCAGGTCGATGTCGGCGGCGAG
>20.58|5740393|32|NZ_CP010833|CRT
GGGTTCGCATACCGGCTGCGCGGGCCGACGTA
>20.59|5740454|37|NZ_CP010833|CRT
ATTTGATCGGCACCGTCGGATGCACCGGCAACTCCTC
>20.60|5740520|32|NZ_CP010833|CRT
CAGGTGATGGGCTCCATCAACTTGTTCGGGGT
>20.61|5740581|32|NZ_CP010833|CRT
TTCGTCTGCGACCGGTGCCATCGCGACATGCG
>20.62|5740642|32|NZ_CP010833|CRT
TCCGCCATTCCCGGACCGATTGCCGATGCCCT
>20.63|5740703|32|NZ_CP010833|CRT
ATTGCGGCCGAGCTCGGCGTCACCTTCGGTGA
>20.64|5740764|32|NZ_CP010833|CRT
TCGGTACTCGGGTGACTCCGGTCGACCACGGT
>20.65|5740825|30|NZ_CP010833|CRT
ACGAGGTGAACGTGGGCGTCGATGAGCCCT
>20.66|5740884|32|NZ_CP010833|CRT
AGGATCGGGATCACGGCGTGCATTCCTACGCC
>20.67|5740945|31|NZ_CP010833|CRT
GCAACGACGTCGTCGTGCCCTGCCAGACGAC
>20.68|5741005|32|NZ_CP010833|CRT
GCTGTCTGGACGGAACTCGACTCCCCCAGGGA

CRISPR arrays and Neighbor proteins around NZ_CP010833_20

CRISPR arrays

The CRISPR arrays of NZ_CP010833_20

>merge|NZ_CP010833|20|5739018-5741065|PILER-CR,CRISPRCasFinder,CRT,PILER-CR
AGTGTGGACCCCGCGCCTGCGGGGATGGTCCGCAGGACCGGGCCCGCGCCAAGGCCCGGAGGAAGTGGACCCCGCGCCTGCGGGGATGGTCCCCCAGCCGGGAGAGACCACTGGGGGCCGTCAGAGTGGACCCCGCGCCTGCGGGGATGGTCCGCCTGACCGGCGCCCTCGTCGCGCCCCGCCTAGGTGGACCCCGCGCCTGCGGGGATGGTCCAGTCCGACCCGGGCCAGCTGAAAGGGAGCGAGGGTGGACCCCGCGCCTGCGGGGATGGTCCTCCGCAGTACGTCCAGTGCTCCGCGTGCAGGACGTGGACCCCGCGCCTGCGGGGATGGTCCGGCCGGTTTGTCGCTGATCCACCGGTAGACCAGGTGGACCCCGCGCCTGCGGGGATGGTCCGAGCGAGGAGAAGCGCCTCGCGGAGCACCGAGCGTGGACCCCGCGCCTGCGGGGATGGTCCGGACTGCGCCGACCGCAACACCCCGCCCCCGGCGTGGACCCCGCGCCTGCGGGGATGGTCCGCCCTTCACGCTGTACGGGGGGAGCGGGAGCGGGTGGACCCCGCGCCTGCGGGGATGGTCTGTACCGGGGCGTCGCCCGCCTGTACTCCTCGCAGTGGACCCCGCGCCTGCGGGGATGGTCCCTGTCGGAGACGCAGCCCGGCAGCTGCTCGATGGTGGACCCCGCGCCTGCGGGGATGGTCCGTTCACGGGTGACGCGCGGCGACTGTTCTTCGGGTGGACCCCGCGCCTGCGGGGATGGTCCGGCATTGCCGTACCTACCGCTTGGCGGGCGTGAGTGGACCCCGCGCCTGCGGGGATGGTCCGGTCTTTCTGACCTGGGGCGTTTCGGTTTCTCCGTGGACCCCGCGCCTGCGGGGATGGTCCGGCCAAGGTCCGGGAGTGGGCGGCCACCCTCGGGTGGACCCCGCGCCTGCGGGGATGGTCCGAGGCTAGACCCGGCCACGGTGGAGGCCGCCCGGTGGACCCCGCGCCTGCGGGGATGGTCCGCCCAGCGCGGCCGAGCCCAGTCCGGCCCGCAGGTGGACCCCGCGCCTGCGGGGATGGTCCGCGGTCCGGGGTTCACCTGATCACCCCCGCCCCCGTGGACCCCGCGCCTGCGGGGATGGTCCCCCGCAGCAGGTCGTCGACTGGATTCAGGCGCAGTGGACCCCGCGCCTGCGGGGATGGTCCGTCGGTGATCGGCCACCTGGAGTGGCAGCCGGGGTGGACCCCGCGCCTGCGGGGATGGTCCGGTCAGCCGCATCAGCGGCCTGCAACTGGGCGGGTGGACCCCGCGCCTGCGGGGATGGTCCGTGCTCCGCTTCCAGGTCGATGTCGGCGGCGAGGTGGACCCCGCGCCTGCGGGGATGGTCCGGGGTTCGCATACCGGCTGCGCGGGCCGACGTAGTGGACCCCGCGCCTGCGGGGATGGTCTGATTTGATCGGCACCGTCGGATGCACCGGCAACTCCTCGTGGACCCCGCGCCTGCGGGGATGGTCCGCAGGTGATGGGCTCCATCAACTTGTTCGGGGTGTGGACCCCGCGCCTGCGGGGGTGGTCCGTTCGTCTGCGACCGGTGCCATCGCGACATGCGGTGGACCCCGCGCCTGCGGGGATGGTCCGTCCGCCATTCCCGGACCGATTGCCGATGCCCTGTGGACCTCGCGTTTGCGGGGATGGTTCGATTGCGGCCGAGCTCGGCGTCACCTTCGGTGAGTGGACCCCGCGCCTGCGGGGATGGTCCGTCGGTACTCGGGTGACTCCGGTCGACCACGGTGTGGACCCCGCGCCTGCGGGGATGGTCCGACGAGGTGAACGTGGGCGTCGATGAGCCCTGGGTGGACCCCGCCTGCGGGGATGGTCCGAGGATCGGGATCACGGCGTGCATTCCTACGCCGTGGACCCGGCGCTCGCCGGGATGGCCGGGCAACGACGTCGTCGTGCCCTGCCAGACGACGTCGACCCCGCGCTTGCAGGGATGGTCCGGCTGTCTGGACGGAACTCGACTCCCCCAGGGAGTGGACCCCGCGCCTGCGGGGATGGTCCA

>NZ_CP010833|20|2|5739018-5739180|PILER-CR
AGTGTGGACCCCGCGCCTGCGGGGATGGTCCGCAGGACCGG	GCCCGCGCCAAGGCCCGGAG
GAAGTGGACCCCGCGCCTGCGGGGATGGTCCCCCAGCCGGG	AGAGACCACTGGGGGCCGTCAGAGT
GGACCCCGCGCCTGCGGGGATGGTCCGCCTGACCGGCGCCCTCGTCGCGCCCCGCCTAGGTGGACCCCGCGCCTGCGGGGATGGTCCAGTCCGACCCGGGCCAGCTGAAAGGGAGCGAGGGTGGACCCCGCGCCTGCGGGGATGGTCC	TCCGCAGTACGTCCAGTGCTCCGCGTGCAGGAC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCCGGTTTGTCGCTGATCCACCGGTAGACCAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GAGCGAGGAGAAGCGCCTCGCGGAGCACCGAGC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGACTGCGCCGACCGCAACACCCCGCCCCCGGC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCCCTTCACGCTGTACGGGGGGAGCGGGAGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCT	GTACCGGGGCGTCGCCCGCCTGTACTCCTCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCC	CTGTCGGAGACGCAGCCCGGCAGCTGCTCGATG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTTCACGGGTGACGCGCGGCGACTGTTCTTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCATTGCCGTACCTACCGCTTGGCGGGCGTGA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGTCTTTCTGACCTGGGGCGTTTCGGTTTCTCC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCCAAGGTCCGGGAGTGGGCGGCCACCCTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GAGGCTAGACCCGGCCACGGTGGAGGCCGCCCG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCCCAGCGCGGCCGAGCCCAGTCCGGCCCGCAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCGGTCCGGGGTTCACCTGATCACCCCCGCCCCC
GTGGACCCCGCGCCTGCGGGGATGGTCC	CCCGCAGCAGGTCGTCGACTGGATTCAGGCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTCGGTGATCGGCCACCTGGAGTGGCAGCCGGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGTCAGCCGCATCAGCGGCCTGCAACTGGGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTGCTCCGCTTCCAGGTCGATGTCGGCGGCGAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGGGTTCGCATACCGGCTGCGCGGGCCGACGTA
GTGGACCCCGCGCCTGCGGGGATGGTCT	GATTTGATCGGCACCGTCGGATGCACCGGCAACTCCTC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCAGGTGATGGGCTCCATCAACTTGTTCGGGGT


>NZ_CP010833|20|18|5739021-5741064|CRISPRCasFinder
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCAGGACCGGGCCCGCGCCAAGGCCCGGAGGAA
GTGGACCCCGCGCCTGCGGGGATGGTCC	CCCAGCCGGGAGAGACCACTGGGGGCCGTCAGA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCCTGACCGGCGCCCTCGTCGCGCCCCGCCTAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	AGTCCGACCCGGGCCAGCTGAAAGGGAGCGAGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	TCCGCAGTACGTCCAGTGCTCCGCGTGCAGGAC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCCGGTTTGTCGCTGATCCACCGGTAGACCAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GAGCGAGGAGAAGCGCCTCGCGGAGCACCGAGC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGACTGCGCCGACCGCAACACCCCGCCCCCGGC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCCCTTCACGCTGTACGGGGGGAGCGGGAGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCT	GTACCGGGGCGTCGCCCGCCTGTACTCCTCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCC	CTGTCGGAGACGCAGCCCGGCAGCTGCTCGATG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTTCACGGGTGACGCGCGGCGACTGTTCTTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCATTGCCGTACCTACCGCTTGGCGGGCGTGA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGTCTTTCTGACCTGGGGCGTTTCGGTTTCTCC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCCAAGGTCCGGGAGTGGGCGGCCACCCTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GAGGCTAGACCCGGCCACGGTGGAGGCCGCCCG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCCCAGCGCGGCCGAGCCCAGTCCGGCCCGCAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCGGTCCGGGGTTCACCTGATCACCCCCGCCCCC
GTGGACCCCGCGCCTGCGGGGATGGTCC	CCCGCAGCAGGTCGTCGACTGGATTCAGGCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTCGGTGATCGGCCACCTGGAGTGGCAGCCGGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGTCAGCCGCATCAGCGGCCTGCAACTGGGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTGCTCCGCTTCCAGGTCGATGTCGGCGGCGAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGGGTTCGCATACCGGCTGCGCGGGCCGACGTA
GTGGACCCCGCGCCTGCGGGGATGGTCT	GATTTGATCGGCACCGTCGGATGCACCGGCAACTCCTC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCAGGTGATGGGCTCCATCAACTTGTTCGGGGT
GTGGACCCCGCGCCTGCGGGGGTGGTCC	GTTCGTCTGCGACCGGTGCCATCGCGACATGCG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTCCGCCATTCCCGGACCGATTGCCGATGCCCT
GTGGACCTCGCGTTTGCGGGGATGGTTC	GATTGCGGCCGAGCTCGGCGTCACCTTCGGTGA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTCGGTACTCGGGTGACTCCGGTCGACCACGGT
GTGGACCCCGCGCCTGCGGGGATGGTCC	GACGAGGTGAACGTGGGCGTCGATGAGCCCT
GGGTGGACCCCGCCTGCGGGGATGGTCC	GAGGATCGGGATCACGGCGTGCATTCCTACGCC
GTGGACCCGGCGCTCGCCGGGATGGCCG	GGCAACGACGTCGTCGTGCCCTGCCAGACGAC
GTCGACCCCGCGCTTGCAGGGATGGTCC	GGCTGTCTGGACGGAACTCGACTCCCCCAGGGA
GTGGACCCCGCGCCTGCGGGGATGGTCC

>NZ_CP010833|20|4|5739021-5741065|CRT
GTGGACCCCGCGCCTGCGGGGATGGTCCG	CAGGACCGGGCCCGCGCCAAGGCCCGGAGGAA
GTGGACCCCGCGCCTGCGGGGATGGTCCC	CCAGCCGGGAGAGACCACTGGGGGCCGTCAGA
GTGGACCCCGCGCCTGCGGGGATGGTCCG	CCTGACCGGCGCCCTCGTCGCGCCCCGCCTAG
GTGGACCCCGCGCCTGCGGGGATGGTCCA	GTCCGACCCGGGCCAGCTGAAAGGGAGCGAGG
GTGGACCCCGCGCCTGCGGGGATGGTCCT	CCGCAGTACGTCCAGTGCTCCGCGTGCAGGAC
GTGGACCCCGCGCCTGCGGGGATGGTCCG	GCCGGTTTGTCGCTGATCCACCGGTAGACCAG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	AGCGAGGAGAAGCGCCTCGCGGAGCACCGAGC
GTGGACCCCGCGCCTGCGGGGATGGTCCG	GACTGCGCCGACCGCAACACCCCGCCCCCGGC
GTGGACCCCGCGCCTGCGGGGATGGTCCG	CCCTTCACGCTGTACGGGGGGAGCGGGAGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCTG	TACCGGGGCGTCGCCCGCCTGTACTCCTCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCCC	TGTCGGAGACGCAGCCCGGCAGCTGCTCGATG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	TTCACGGGTGACGCGCGGCGACTGTTCTTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	GCATTGCCGTACCTACCGCTTGGCGGGCGTGA
GTGGACCCCGCGCCTGCGGGGATGGTCCG	GTCTTTCTGACCTGGGGCGTTTCGGTTTCTCC
GTGGACCCCGCGCCTGCGGGGATGGTCCG	GCCAAGGTCCGGGAGTGGGCGGCCACCCTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	AGGCTAGACCCGGCCACGGTGGAGGCCGCCCG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	CCCAGCGCGGCCGAGCCCAGTCCGGCCCGCAG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	CGGTCCGGGGTTCACCTGATCACCCCCGCCCCC
GTGGACCCCGCGCCTGCGGGGATGGTCCC	CCGCAGCAGGTCGTCGACTGGATTCAGGCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCCG	TCGGTGATCGGCCACCTGGAGTGGCAGCCGGG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	GTCAGCCGCATCAGCGGCCTGCAACTGGGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	TGCTCCGCTTCCAGGTCGATGTCGGCGGCGAG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	GGGTTCGCATACCGGCTGCGCGGGCCGACGTA
GTGGACCCCGCGCCTGCGGGGATGGTCTG	ATTTGATCGGCACCGTCGGATGCACCGGCAACTCCTC
GTGGACCCCGCGCCTGCGGGGATGGTCCG	CAGGTGATGGGCTCCATCAACTTGTTCGGGGT
GTGGACCCCGCGCCTGCGGGGGTGGTCCG	TTCGTCTGCGACCGGTGCCATCGCGACATGCG
GTGGACCCCGCGCCTGCGGGGATGGTCCG	TCCGCCATTCCCGGACCGATTGCCGATGCCCT
GTGGACCTCGCGTTTGCGGGGATGGTTCG	ATTGCGGCCGAGCTCGGCGTCACCTTCGGTGA
GTGGACCCCGCGCCTGCGGGGATGGTCCG	TCGGTACTCGGGTGACTCCGGTCGACCACGGT
GTGGACCCCGCGCCTGCGGGGATGGTCCG	ACGAGGTGAACGTGGGCGTCGATGAGCCCT
GGGTGGACCCCGCCTGCGGGGATGGTCCG	AGGATCGGGATCACGGCGTGCATTCCTACGCC
GTGGACCCGGCGCTCGCCGGGATGGCCGG	GCAACGACGTCGTCGTGCCCTGCCAGACGAC
GTCGACCCCGCGCTTGCAGGGATGGTCCG	GCTGTCTGGACGGAACTCGACTCCCCCAGGGA
GTGGACCCCGCGCCTGCGGGGATGGTCCA

>NZ_CP010833|20|3|5739265-5740579|PILER-CR
	GCCCGCGCCAAGGCCCGGAG
GAAGTGGACCCCGCGCCTGCGGGGATGGTCCCCCAGCCGGG	AGAGACCACTGGGGGCCGTCAGAGT
GGACCCCGCGCCTGCGGGGATGGTCCGCCTGACCGGCGCCCTCGTCGCGCCCCGCCTAGGTGGACCCCGCGCCTGCGGGGATGGTCCAGTCCGACCCGGGCCAGCTGAAAGGGAGCGAGGGTGGACCCCGCGCCTGCGGGGATGGTCC	TCCGCAGTACGTCCAGTGCTCCGCGTGCAGGAC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCCGGTTTGTCGCTGATCCACCGGTAGACCAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GAGCGAGGAGAAGCGCCTCGCGGAGCACCGAGC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGACTGCGCCGACCGCAACACCCCGCCCCCGGC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCCCTTCACGCTGTACGGGGGGAGCGGGAGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCT	GTACCGGGGCGTCGCCCGCCTGTACTCCTCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCC	CTGTCGGAGACGCAGCCCGGCAGCTGCTCGATG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTTCACGGGTGACGCGCGGCGACTGTTCTTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCATTGCCGTACCTACCGCTTGGCGGGCGTGA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGTCTTTCTGACCTGGGGCGTTTCGGTTTCTCC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGCCAAGGTCCGGGAGTGGGCGGCCACCCTCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GAGGCTAGACCCGGCCACGGTGGAGGCCGCCCG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCCCAGCGCGGCCGAGCCCAGTCCGGCCCGCAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCGGTCCGGGGTTCACCTGATCACCCCCGCCCCC
GTGGACCCCGCGCCTGCGGGGATGGTCC	CCCGCAGCAGGTCGTCGACTGGATTCAGGCGCA
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTCGGTGATCGGCCACCTGGAGTGGCAGCCGGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGTCAGCCGCATCAGCGGCCTGCAACTGGGCGG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GTGCTCCGCTTCCAGGTCGATGTCGGCGGCGAG
GTGGACCCCGCGCCTGCGGGGATGGTCC	GGGGTTCGCATACCGGCTGCGCGGGCCGACGTA
GTGGACCCCGCGCCTGCGGGGATGGTCT	GATTTGATCGGCACCGTCGGATGCACCGGCAACTCCTC
GTGGACCCCGCGCCTGCGGGGATGGTCC	GCAGGTGATGGGCTCCATCAACTTGTTCGGGGT
GTGGACCCCGCGCCTGCGGGGGTGGTCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075266607.1|5752970_5754203_-|NarK/NasA-family-nitrate-transporter	unknown	unknown	gnl|CDD|225133
NZ_CP010833.1|WP_003969335.1|5727141_5727447_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266596.1|5737674_5738697_+|type-I-E-CRISPR-associated-endonuclease-Cas1	cas1	cd09719_cas1_CAS-I-E	gnl|CDD|274693
NZ_CP010833.1|WP_075266604.1|5746420_5747980_-|acyl-CoA-synthetase	unknown	unknown	gnl|CDD|236096
NZ_CP010833.1|WP_075266602.1|5744290_5744914_+|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_075266600.1|5742090_5743356_+|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP010833.1|WP_075266589.1|5728182_5728743_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266601.1|5743445_5744186_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235500
NZ_CP010833.1|WP_075266591.1|5732378_5734085_+|type-I-E-CRISPR-associated-protein-Cse1/CasA	cas8e	pfam09481_cas8e_CAS-I-E	gnl|CDD|378189
NZ_CP010833.1|WP_079181540.1|5729127_5732100_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|182031
NZ_CP010833.1|WP_075266597.1|5738693_5739002_+|type-I-E-CRISPR-associated-endoribonuclease-Cas2	cas2	pfam09707_cas2_CAS-I-E	gnl|CDD|378244
NZ_CP010833.1|WP_075266599.1|5741618_5741975_+|VapC-toxin-family-PIN-domain-ribonuclease	unknown	unknown	gnl|CDD|350322
NZ_CP010833.1|WP_075266594.1|5736106_5736907_+|type-I-E-CRISPR-associated-protein-Cas5/CasD	cas5	cd09756_cas5_CAS-I-E	gnl|CDD|378243
NZ_CP010833.1|WP_075266593.1|5734955_5736110_+|type-I-E-CRISPR-associated-protein-Cas7/Cse4/CasC	cas7	pfam09344_cas7_CAS-I-E	gnl|CDD|378153
NZ_CP010833.1|WP_075266598.1|5741391_5741622_+|type-II-toxin-antitoxin-system-VapB-family-antitoxin	unknown	unknown	gnl|CDD|378324
NZ_CP010833.1|WP_075266592.1|5734241_5734847_+|type-I-E-CRISPR-associated-protein-Cse2/CasB	cse2gr11	cd09670_cse2gr11_CAS-I-E	gnl|CDD|378191
NZ_CP010833.1|WP_075266603.1|5744910_5746428_-|acetyl-CoA-carboxylase	unknown	unknown	gnl|CDD|223895
NZ_CP010833.1|WP_075266595.1|5736903_5737668_+|type-I-E-CRISPR-associated-protein-Cas6/Cse3/CasE	cas6e	pfam08798_cas6e_CAS-I-E:CAS-IV	gnl|CDD|378050
NZ_CP010833.1|WP_075266605.1|5748246_5750736_+|carbohydrate-binding-protein	unknown	unknown	gnl|CDD|271150
NZ_CP010833.1|WP_075266606.1|5750732_5752910_+|carbohydrate-binding-protein	unknown	unknown	gnl|CDD|211415

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP010833.1|WP_075266597.1|5738693_5739002_+|type-I-E-CRISPR-associated-endoribonuclease-Cas2	cas2	pfam09707_cas2_CAS-I-E	1.7e-32	106.1	0.0
NZ_CP010833.1|WP_075266596.1|5737674_5738697_+|type-I-E-CRISPR-associated-endonuclease-Cas1	cas1	cd09719_cas1_CAS-I-E	9.9e-104	340.9	0.1
NZ_CP010833.1|WP_075266593.1|5734955_5736110_+|type-I-E-CRISPR-associated-protein-Cas7/Cse4/CasC	cas7	pfam09344_cas7_CAS-I-E	3.7e-107	353.7	2.6
NZ_CP010833.1|WP_075266592.1|5734241_5734847_+|type-I-E-CRISPR-associated-protein-Cse2/CasB	cse2gr11	cd09670_cse2gr11_CAS-I-E	1.6e-30	101.2	3.4
NZ_CP010833.1|WP_075266595.1|5736903_5737668_+|type-I-E-CRISPR-associated-protein-Cas6/Cse3/CasE	cas6e	pfam08798_cas6e_CAS-I-E:CAS-IV	1.3e-59	196.5	0.0
NZ_CP010833.1|WP_079181540.1|5729127_5732100_+|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	5.8e-56	184.8	0.0
NZ_CP010833.1|WP_075266594.1|5736106_5736907_+|type-I-E-CRISPR-associated-protein-Cas5/CasD	cas5	cd09756_cas5_CAS-I-E	4.3e-52	171.2	1.0
NZ_CP010833.1|WP_075266591.1|5732378_5734085_+|type-I-E-CRISPR-associated-protein-Cse1/CasA	cas8e	pfam09481_cas8e_CAS-I-E	2.7e-95	314.8	5.9

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075266607.1|5752970_5754203_-|NarK/NasA-family-nitrate-transporter	gnl|CDD|225133	COG2223, NarK, Nitrate/nitrite transporter [Inorganic ion transport and metabolism].	3.54581e-83
NZ_CP010833.1|WP_075266600.1|5742090_5743356_+|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	9.23149e-69
NZ_CP010833.1|WP_075266596.1|5737674_5738697_+|type-I-E-CRISPR-associated-endonuclease-Cas1	gnl|CDD|274693	TIGR03638, cas1_ECOLI, CRISPR-associated endonuclease Cas1, subtype I-E/ECOLI. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the ECOLI subtype of CRISPR/Cas system.	7.65889e-127
NZ_CP010833.1|WP_075266604.1|5746420_5747980_-|acyl-CoA-synthetase	gnl|CDD|236096	PRK07787, PRK07787, acyl-CoA synthetase; Validated.	0
NZ_CP010833.1|WP_075266602.1|5744290_5744914_+|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.28025e-09
NZ_CP010833.1|WP_075266601.1|5743445_5744186_-|SDR-family-oxidoreductase	gnl|CDD|235500	PRK05557, fabG, 3-ketoacyl-(acyl-carrier-protein) reductase; Validated.	1.44237e-80
NZ_CP010833.1|WP_075266606.1|5750732_5752910_+|carbohydrate-binding-protein	gnl|CDD|211415	cd11574, GH99, Glycoside hydrolase family 99, an endo-alpha-1,2-mannosidase. This family of glycoside hydrolases 99 (following the CAZY nomenclature) includes endo-alpha-1,2-mannosidase (EC 3.2.1.130), which is an important membrane-associated eukaryotic enzyme involved in the maturation of N-linked glycans. Specifically, it cleaves mannoside linkages internal to N-linked glycan chains by hydrolyzing an alpha-1,2-mannosidic bond between a glucose-substituted mannose and the remainder of the chain. The biological function and significance of the soluble bacterial orthologs, which may have obtained the genes via horizontal transfer, is not clear.	2.18127e-109
NZ_CP010833.1|WP_075266591.1|5732378_5734085_+|type-I-E-CRISPR-associated-protein-Cse1/CasA	gnl|CDD|378189	pfam09481, CRISPR_Cse1, CRISPR-associated protein Cse1 (CRISPR_cse1). Clusters of short DNA repeats with non-homologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This entry, represented by CT1972 from Chlorobaculum tepidum, is found in the CRISPR/Cas subtype Ecoli regions of many bacteria (most of which are mesophiles), and not in Archaea. It is designated Cse1.	7.39672e-96
NZ_CP010833.1|WP_079181540.1|5729127_5732100_+|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|182031	PRK09694, PRK09694, CRISPR-associated helicase/endonuclease Cas3.	5.79001e-72
NZ_CP010833.1|WP_075266597.1|5738693_5739002_+|type-I-E-CRISPR-associated-endoribonuclease-Cas2	gnl|CDD|378244	pfam09707, Cas_Cas2CT1978, CRISPR-associated protein (Cas_Cas2CT1978). This entry represents a minor branch of the Cas2 family of CRISPR-associated protein which are found in IPR003799. Cas proteins are found adjacent to a characteristic short, palindromic repeat cluster termed CRISPR, a probable mobile DNA element.	7.22978e-44
NZ_CP010833.1|WP_075266599.1|5741618_5741975_+|VapC-toxin-family-PIN-domain-ribonuclease	gnl|CDD|350322	cd18755, PIN_MtVapC3_VapC21-like, VapC-like PIN domain of Mycobacterium tuberculosis VapC3, VapC21 and related proteins. This subfamily includes the Virulence associated protein C (VapC)-like PIN (PilT N terminus) domain of Mycobacterium tuberculosis VapC3 and VapC21 toxins. It belongs to the VapC-like family of the PIN domain nuclease superfamily. VapC is a PIN-domain ribonuclease toxin from prokaryotic VapBC toxin-antitoxin (TA) systems. VapB is a transcription factor-like protein antitoxin acting as an inhibitor. Other members of the VapC-like nuclease family include FitB toxin of the FitAB TA system, eukaryotic ribonucleases such as Smg6, ribosome assembly factor NOB1, exosome subunit Rrp44 endoribonuclease and rRNA-processing protein Fcf1. The structural properties of the PIN domain indicate its active center, consisting of three highly conserved catalytic residues which coordinate metal ions; in some members, additional metal coordinating residues can be found while some others lack several of these key catalytic residues. The PIN active site is geometrically similar in the active center of structure-specific 5' nucleases, PIN-domain ribonucleases of eukaryotic rRNA editing proteins, and bacterial toxins of toxin-antitoxin (TA) operons.	7.63837e-14
NZ_CP010833.1|WP_075266594.1|5736106_5736907_+|type-I-E-CRISPR-associated-protein-Cas5/CasD	gnl|CDD|378243	pfam09704, Cas_Cas5d, CRISPR-associated protein (Cas_Cas5). CRISPR is a term for Clustered, Regularly Interspaced Short Palindromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum.	2.49923e-40
NZ_CP010833.1|WP_075266593.1|5734955_5736110_+|type-I-E-CRISPR-associated-protein-Cas7/Cse4/CasC	gnl|CDD|378153	pfam09344, Cas_CT1975, CT1975-like protein. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This family is represented by CT1975 of Chlorobium tepidum.	1.09657e-134
NZ_CP010833.1|WP_075266598.1|5741391_5741622_+|type-II-toxin-antitoxin-system-VapB-family-antitoxin	gnl|CDD|378324	pfam09957, VapB_antitoxin, Bacterial antitoxin of type II TA system, VapB. VapB is the antitoxin of a bacterial toxin-antitoxin gene pair. The cognate toxin is VapC, pfam05016. The family contains several related antitoxins from Cyanobacteria and Actinobacterial families. Antitoxins of this class carry an N-terminal ribbon-helix-helix domain, RHH, that is highly conserved across all type II bacterial antitoxins, which dimerizes with the RHH domain of a second VapB molecule. A hinge section follows the RHH, with an additional pair of flexible alpha helices at the C-terminus. This C-terminus is the Toxin-binding region of the dimer, and so is specific to the cognate toxin, whereas the RHH domain has the specific function of lying across the RNA-binding groove of the toxin dimer and inactivating the active-site - a more general function of all antitoxins.	1.39076e-08
NZ_CP010833.1|WP_075266592.1|5734241_5734847_+|type-I-E-CRISPR-associated-protein-Cse2/CasB	gnl|CDD|378191	pfam09485, CRISPR_Cse2, CRISPR-associated protein Cse2 (CRISPR_cse2). Clusters of short DNA repeats with non-homologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This family of proteins, represented by CT1973 from Chlorobaculum tepidum, is encoded by genes found in the CRISPR/Cas subtype Ecoli regions of many bacteria (most of which are mesophiles), and not in Archaea. It is designated Cse2.	7.22744e-33
NZ_CP010833.1|WP_075266603.1|5744910_5746428_-|acetyl-CoA-carboxylase	gnl|CDD|223895	COG0825, AccA, Acetyl-CoA carboxylase alpha subunit [Lipid metabolism].	1.29715e-46
NZ_CP010833.1|WP_075266595.1|5736903_5737668_+|type-I-E-CRISPR-associated-protein-Cas6/Cse3/CasE	gnl|CDD|378050	pfam08798, CRISPR_assoc, CRISPR associated protein. This domain forms an anti-parallel beta strand structure with flanking alpha helical regions.	4.83277e-71
NZ_CP010833.1|WP_075266605.1|5748246_5750736_+|carbohydrate-binding-protein	gnl|CDD|271150	cd04084, CBM6_xylanase-like, Carbohydrate Binding Module 6 (CBM6); many are appended to glycoside hydrolase (GH) family 11 and GH43 xylanase domains. This family includes carbohydrate binding module 6 (CBM6) domains that are appended mainly to glycoside hydrolase (GH) family domains, including GH3, GH11, and GH43 domains. These CBM6s are non-catalytic carbohydrate binding domains that facilitate the strong binding of the GH catalytic modules with their dedicated, insoluble substrates. Examples of proteins having CMB6s belonging to this family are Microbispora bispora GghA, a 1,4-beta-D-glucan glucohydrolase (GH3); Clostridium thermocellum xylanase U (GH11), and Penicillium purpurogenum ABF3, a bifunctional alpha-L-arabinofuranosidase/xylobiohydrolase (GH43). GH3 comprises enzymes with activities including beta-glucosidase (hydrolyzes beta-galactosidase) and beta-xylosidase (hydrolyzes 1,4-beta-D-xylosidase). GH11 family comprises enzymes with xylanase (endo-1,4-beta-xylanase) activity which catalyze the hydrolysis of beta-1,4 bonds of xylan, the major component of hemicelluloses, to generate xylooligosaccharides and xylose. GH43 includes beta-xylosidases and beta-xylanases, using aryl-glycosides as substrates. CBM6 is an unusual CBM as it represents a chimera of two distinct binding sites with different modes of binding: binding site I within the loop regions and binding site II on the concave face of the beta-sandwich fold.	2.48425e-35

Protein sequences

>NZ_CP010833.1|WP_075266597.1|5738693_5739002_+|type-I-E-CRISPR-associated-endoribonuclease-Cas2
MTVIILIAAPAGLRGHLTRWMVEASAGVFVGNPSRRIRDRLWELLATRIGDGQAILIEPAANEQGWAVRTAGRDRWQPVDFDGLILSARPKNPPNENSHPAR
>NZ_CP010833.1|WP_075266596.1|5737674_5738697_+|type-I-E-CRISPR-associated-endonuclease-Cas1
MPDIWWKADPQDLHRLVDRVSSVYVERSHLDRDENAVVIINKRQTVRVPAAMVAVMLLGPGTRVTHGAIRLLADSGTAVCWVGEQGVRMYAAGLGPSRGAGLLHRQAWLVTRPKERLSVARAMYGMRFPGEDVSALTMQQLRGREGTRIKKLYRAQADRTGVAWNGRVYKAGDACAAGDDLNRLLSAANAALYGICHAVIIGLGASPGLGFVHTGKATSFVLDIADLYKAEYTIPLAFDLAAQGLTEERDARLGLRDLIARDKLLGRIVTDVKTLLSPEGTDFDAPEANSLWDESVGAVPGGTNYASHADLSAHGMTDNHIAVIGPEPHETEPHETEPTS
>NZ_CP010833.1|WP_075266595.1|5736903_5737668_+|type-I-E-CRISPR-associated-protein-Cas6/Cse3/CasE
MTDMPYLSRIRINPLRAESRKLLASPRAMHAAVEGGLPGVPEEARTLWRLDQDNPHRPHLFVLSTGAPDWNHLVEQAGWPGADGDHYAVRGYAPLLRQLAPGRSFAFRLTANPVQNTSRPDKPTERQQSRIDDGGRRRGFRLGHRTAAAQLNWFLTRTAKWGFDVPAAPHLEGIGGADNEPPRDIRITARQRRSFKKGAVTAKEAHVVLNAVTFEGRLRVTDPALLTERLLGGIGPSKAYGCGLLTLAPLAERE
>NZ_CP010833.1|WP_075266594.1|5736106_5736907_+|type-I-E-CRISPR-associated-protein-Cas5/CasD
MTPRVPTSVLLLRLAAPLQSWGDRSSPLNRRETRPEPTKSGVVGLLAAAAGRSRHAPLDDLTGLALGIRIDQPGSLLRDYHTVSDYRGQPLLSAAVNTKGLQKPTSPAKRTHITQRFYLQDAVFLAAVEGPQELIATLEHAVRHPAFPLALGRRSCAPSQPLALGQRSGSLEDVLREEPWQAARAVRRRWGRANGDAPHVRLPATLDDPAGDEVRDDVPLSFAPAGRAFTTRRTRHTYLEVPTGLTPDPHRPGNTGGHDPFALLGW
>NZ_CP010833.1|WP_075266593.1|5734955_5736110_+|type-I-E-CRISPR-associated-protein-Cas7/Cse4/CasC
MTQRMYIDVHVVQTVPPANLNRDDQGNPKEAVYGGVRRSRVSSQAWKRAARQHFDTRAAEPDRATRTKRIIGELGRRISRNTGLDREDADRISTALLAQLGLSQGKKAGDTAYLLFYGNAQLDAVGALVNDRAADLAALDDKALAEAVKELPVAEHFQAGHPVGVALFGRMVADIPKLNVDAAVQVAHALSTHETQLEFDYYTAVDDQNEKDETGAGMIGTIGFNSATLYRYATVGFAQLAENLGGDTEAALDALDRFVDSFALSAPTGYQNSFAHRTRPSLVAVVVRTDQPVNLVSAFEEPVAAEAGIQANSARRLAEEHLTAAQVWGDTPLYSAASHTFTDRERRTKDTVETLTQAFGEPVSFADLRTTLRTRIATALGDQA
>NZ_CP010833.1|WP_075266592.1|5734241_5734847_+|type-I-E-CRISPR-associated-protein-Cse2/CasB
MTEEDFTKQRIWHRYISADGTWRRKEGSPAERRPPGEDLAVLRRGLGCPAGTVLEMFAFYTCPVDDFAARRGEVSAQQEAEHAALALYGLHQQSQDRPMHRDGVGLGRALLALRRHERTSEEAVDSRFRQAFSATSAAALQLRLRGLITQLKDIKQPLDYNRLAADIHDWNRPESRSRVRRRWGLDYYGWTQTAESPRRGR
>NZ_CP010833.1|WP_075266591.1|5732378_5734085_+|type-I-E-CRISPR-associated-protein-Cse1/CasA
MVHGFSLTDDPWLLLPSVDGAPARERSLRTALLEAHEFGDLVVEIPTQRAAVFRQLLLPVILDALGRPADEREWVSWYSTGRWIPEQRRKIEAYLDTHRALFDLFDQVNPFGQVADLRTAKGETKSAGLIVATAAQGNNVPLFASRTEGDVFPLTPAQAAHWLMHTQCWDTAAIKTGAVGDPNAKSGKTVGNPTGPLGQMGVTLLIGTTLFETLLLNLPVGAPPMSTDLPQWRRRDAGAPRSVATPQWDTRVPEGLLDLWTWQSRRIRLFPETSDEGLRVTRVLVAAGDRMPHTPETEPHTMWRLEPTGGRSSARGRGGTVLPRRPLRLQPGKAAWRGLDALLAPERQSREAGERTSGFATSKLLDQAGALVPELGESYPLRVELSGVAYGNQSAVIDDVMFDALPLPLAALDSGSVVRAALLEVAEQGEQLATAVNHLSADLRRALGAEPIPWDKGQRPGELVLHALDPLVRRLLTGMRGVEDLERVEAGQLAWEQLAWRRSWETADRLLRAVPVGAFVGRSVSQGEGKPERTYRASLAEASFLRRRAEILHRAEAVRRSSGNPDSE
>NZ_CP010833.1|WP_079181540.1|5729127_5732100_+|CRISPR-associated-helicase/endonuclease-Cas3
MGCQWRPLRSGAFRPSAGSVVDLQQLSAHHEPFAVRALETLWGKSQERAGGTTNLLMAHLLDTAAVAELLWDGLLAGSTRSALEEIAGGPGLGRRMFAWLCGLHDCGKATPVHQRLWPEGADAVRRSGLTWVETAAVAGVKKQKRWRHDWAGGLIVRELLAPAHWDPEQVDWVWPLVAGHHGAFPSLRDVQEPKPAKGQLRGTGPWRQVQQAVLDVFTAELGFENLGDVQPTVVPSRALQLQLSGLVVMADWIASDERFFTGLDDLGRVSLEASRVRAASAWQALGLQRGWGSLELPGPEAFRDRFGYAPRPSQGMVVDAAHKMGGPGLMVIEAPMGEGKTEAAQAATEVLAARFGADGVFVGMPTQATSDPMFTRTRRWVGSIDPDSASRVVLLHGKRAFNHEWKILLENAGNSLDEAFHGVDEFGMDDDPYGVGAEVCGEQERNAPAEWFLGPKRGLLAPFVVGTVDQLLYAATRTRHVMLRMAGLAGKIVVLDEIHACDVYMSQFLAEALRWLGQAGVPVVVLSATLAPAQRQTLFDAYLAGAASREEYRAEIPAPRGYPRVTTAWLPTSGSARFHVDATSSWREDLDVAVRVVPEKVPGARCTREERERLQVEADRGVGDLLASELADGGTALVIRNSVARAQSLYGELRERFPDDEVRLLHARFTVSRRADLTEESLRLLGPDAPRSRGRRLILVATQLAEQSFDVDADLLITDLAPVDLLLQRMGRLHRHEKTWRPDRLRAPQVFVTGFEPRAGREPAFAFAGEMIYGRHLLLRTAAVLPGAGEKWSVPVDVPTLVEKVYDADVPLLPESWQPAGDVAGCEQSDRDRARAEEARQFLLSPQGDHERRTLAGLHYGGSSAGSDEGSLQAAVRDGDQSVEVVLVVRDGEDSVYRTLAGRNLSVNGDVSADVLDEVLGSAVRLPPKYTESALKLSPLPGWYGHPWLRRSRALVMDASRTARLAEFTVSYDDEFGLRQIKTPIDEGIR
>NZ_CP010833.1|WP_075266589.1|5728182_5728743_-|hypothetical-protein
MSVRGSLRRHRFISTAVALAATVSACSGDEPPEKAYTVPGSLCGIAVEPALVKAVLPGGDSLTSATQKPNGGTVRCNLYVDDTLVLSLTQAWWSEGKATAAVSPAYPGTKDGTMSEDERFIYSGEAGVGRTVPSCETSEHPEQDLYTAVETRDTGIDDPEAIEKLLTAYTKAVEGSAACREPAAGS
>NZ_CP010833.1|WP_003969335.1|5727141_5727447_-|hypothetical-protein
MRYRLTFIAGVALGYVLGTRAGRERYEQLKKSARQFTENPAVRNAAESAAHSGRDIAGKAYHSVSDKVGDKVPASVAERVRSLRDRSSQNGFEDDWGTTNT
>NZ_CP010833.1|WP_075266598.1|5741391_5741622_+|type-II-toxin-antitoxin-system-VapB-family-antitoxin
MSGTRIDLDDEALAEAMRLMGTSTKKETVNGALRDYVARIKRLEGAEKLAACGEKGEFEAAAAHVAAKRARRAVFE
>NZ_CP010833.1|WP_075266599.1|5741618_5741975_+|VapC-toxin-family-PIN-domain-ribonuclease
MITYLLDTSARWHLFRTPGGLRPWEGHITAGVFHICEPTRTEFPCSATSPARRDGLAEELDGLCLLSPVPKRSTSSPNEHSTAQHRAAGANGLLLDVDNDFAAAGTVLKEVQQRDVRV
>NZ_CP010833.1|WP_075266600.1|5742090_5743356_+|MFS-transporter
MTESAEPRAPRTHILADLTPLRTSPDYRRLWFGNTVSWIGQGMTALAVSLQVYDITGSAFSVGLIGFCSLVPLVVFGLYGGAVADTVDRRKLGLFSAAGSFGLSLVLVAATVVGIEQVGLLYAIVALQAVCFALNAPARSSMIARLLPAEQLPAANALTTMTSTTGTLVGPMLGGLIVGWWGYRAAYTVDAVCFTASLYAMWRMPSMLPDRKDGDAGKRASVLDGLRFLGTRPNLRMTFFSDLCAMVLAHPRALFPAVAVLWYGGDARTTGLLVAAPALGALLGGVFSGWLGRIRRHGLAILLAVGSWGAAIAVFGLTRNLWLGLLFLALAGCADTVSMVFRNTMLQAAVPDELRGRLQGVFIVVVAGGPRLGDFLAGSVADLASPAVAVTGGGILCVTAVTLLALKWRAFARYDARDPQP
>NZ_CP010833.1|WP_075266601.1|5743445_5744186_-|SDR-family-oxidoreductase
MSQLEGRAALVTGGSRGIGAATALRLAEGGADVALTYVNAADKAAEVVAAIEALGRRAVAVRADSADPAAVADSVGKTAAAFGRLDILVNNAGVFPFGPVEEAPLAEIDRTLAVNVRAVYLATQAALPHMGHGGRVISIGSCWGARVPVPNVALYAMSKSALVGFTKGLAHDVAPKGITANIVDPGPTVTDMNPAGTDVAEAERLRTAAKVMGADVDIANAVAFLASPEGQWITGTTLAVDGGYTA
>NZ_CP010833.1|WP_075266602.1|5744290_5744914_+|TetR/AcrR-family-transcriptional-regulator
MAERGRPRAFDRTVALRGAMEVFWELGYEGTKLTDLTGAMNINSASLYNTFGSKEQLFREAVALYGSTTGSATARALREEPTARGAVEAMLRGNIDIFADPGTPGGCMIVLAAANCAHQNRSVAEHLAGHRRRTVAELEERLERAVSEGELAPEIDVRSVADFYATILYGLSIEARDGVPVERLRATVDRAVGLWDTLVRPGPDERA
>NZ_CP010833.1|WP_075266603.1|5744910_5746428_-|acetyl-CoA-carboxylase
MPDADSARATAREAIALLTGAAGFTEHRPPPRPLPPDGPLGWAGYDAARERASARTGEEESVVYGTGVVGDRACVLLSFEFGFLGGSLGRNTGDRLAAAYELALTRRLPLLALVATGGSRMQEGMVALTQLQRVAAASTRLRAAGLPQIAVVRDPTTGGGWATVGAGADVVLALPGAQVGFAGSRVRPPDADPSAYSAEGQFAAGQVDAVVPADELAAAVTQWLRALGPHENLPAAPVPRALPTAGAGTGSTAGVSTGAGAGTGSTAGVSTGAGAGTGSTAGVSTSPGAGTPSAAGGGAVAPLPETGREAVARARDPRRPRAEAYLADYFAVRLPLHGDRSGATDPGLLCGLGLRADGQPVAYVAQCGTPTRPAGYRAAARTVRLADRLGVPVLTLVDTPGAANDAEAERAGAGAAIADTFAAIAAARVPVTTLVIGEGGSGGALALAAPDNTHVTVDSYFSVIAPELAAAILKRPPSETGATADQLRLRPQDLVDLGFARSIVG
>NZ_CP010833.1|WP_075266604.1|5746420_5747980_-|acyl-CoA-synthetase
MTLLLPALQSPTGPAASREAVRFGDLSLTYGDLAVASTALAARIADAGRVAVWATPTPETVIAVVAALRAGVPVVPLNPRTGESELAHILADSEPTAVLAGPDDELPPGLEKLRRVTVDARTAGASGALEGSEAYGAAPGVSAMGKADGAGEARPAAYGIGEAGPEDPALIVYTSGTTGPPKGAVLPRRAVAASLDALEDAWEWTGDDVLVHALPLFHVHGLILGVLGPLRRGGSVRHLGKFSPDGVARELGSGGTMLFGVPTMYHRLAEVLDGSASDAERGSLTRALSGARLLVSGSAALPVHDHERIAAATGRRVIERYGMTETLMNTGIRADGAPRPGTVGPPLAGVELRLAEEDGTVLDEPGAIGEIQVRGPNLFTGYLNRPDATAAAHTTDGWFRTGDVGTVDADGYVTIVGRKATDLIKSGGYKIGAGEIENVLLAHPGVREVAVTGEEDPDLGERVVAWVVATDPGSPPSPEELADRVAAQLAPHKRPRTVRYLDALPRNDLGKIMKRSLRA
>NZ_CP010833.1|WP_075266605.1|5748246_5750736_+|carbohydrate-binding-protein
MSPAPPRWSRYATALAALLAATLAVPTAGPALAADPETRAPRIAADIPAADYQQVQLALGAAELGEAMSLAVLPDRSVLHTARDGTVRLTDAAGSTKTAGKLDVYTHDEEGLQGIAVDPDFTANRFVYLYYSPLLNTPPGDAPTTGSAADFEAWKGHLNLSRFVLKADGTLDLGSEKVVLEVESDRGQCCHVGGDIDFDAAGNLYLTTGDDTNPFESAGYAPIDERTDRNPQFDAQRSSGNTNDLRGKLLRIKPTADGGYTVPAGNLFAPGTADTRPEIYAMGFRNPFRMSVDKKTGAVYIGDYGPDAGTTDPNRGPSGQVEFNRVTEPGNFGWPYCTGTNTLTETYGEYTFPSGPSGAKYDCASGPANNSFRNTGLATLPPAQPAWIRYAGDAGSPPEFGGGSESPMAGPVYNFDADLDSAVKFPASLDGRFFATEYGRKWIKPVEVKADGSPGTIDTFPWTGTQVMDSAFGPDGALYVLDYGTGTNNQALYRVEYLAGSNRSPVAKAAADRTSGPTPLTVSFSSAGSTDPEGGNLTHAWDFGDGTTSTDPNPSHTYTTAGTYNPTLTVTDPEGLTGTASLVVTAGNTAPTVTLTTPADGSLFSFGDSVPFTVTVSDPEDGTVDCSKVKVTYLLGHDSHRHQITSKNGCSGTIDVPVDGEHDSAANIYGVFDAEYTDAGGLTTHSDSILQPRHRQGEHFAAQNGIEIAPHGSAEGGSAVGYTDDGDWVSFTPYVLSNATSITARVASGGAGGTLEVRVGSPTGTLLSSLPVAPTGGWENYVDVTADVDNAPAGSTELFFVFTGPTGQGSLFDLDAFTFSTQGAQVNDR
>NZ_CP010833.1|WP_075266606.1|5750732_5752910_+|carbohydrate-binding-protein
MRRSRTRTRSRLACAVALALGAAFLSPGVPSAAAADPYQVLVFSKTAGFRHDSIPAGIAALQQLGADNDFTVTATEDATAFTPQNLAEYEAVVFLSTTGDVLDDTQQSALKGYVDGGGGFVGVHAAADTEYDWPEYEDLVGAWFQSHPAIQEARLTTEDHVHPATAHLDDTWTRTDEWYNYRSNPRDSVHVLQSLDESSYSGGEMGGDHPITWCHEQQEGRSFYTGLGHTIESFADPDFRQLLLGGVQYAAGAVEADCTAGDPGPGPGGDSAEAEAYTSSSGVQSAAHGSASGGATLGYIDDGDWAGYSSLDTAGATAFTATVSSAGAGGTIEVRSGSATGPLLGSVDVTPTGGWETFTEVTTTLTAGTGPLFLRFTGGAGALFDIDRFTLTRAPATEDEGSSNVHLFYYPWYGTPDGPAGSWRHWQQGGHTPPDSIGADLYPKLGPYDSGDIAGAVDQHMEWVKRSGAGVIVYSWWGQGGYEDGIAGDVMDAAARHGIEVAWHIEPYGGRTAASVVDDIAYLEGKFGDHPAFYRDAAHGDRNAYYIFESLKIQDWSALDAVKDTAIVLAQTTDTSKVDHFGGIYTYDGIAGATAPGWKNAGDHAKANGLVWAPSVAPGYIDDRAVPGNTTPTLGREDGASYDLEWNNALDPAIGGDPTWVSVTSFNEWHEGSSIEPASSTPPPGHGYATFEGAYGKTGEAAETAYLDRTAYWADRFEQQLRQRR
>NZ_CP010833.1|WP_075266607.1|5752970_5754203_-|NarK/NasA-family-nitrate-transporter
MDNSVKQSPEPPASPAPAAAAPSPAAYRNLVLATVGFALTFWAWNLIAPMSGDYKDRLGLSSFQQSFLVAVPVLVGSLGRIPVGALTDKYGAKLMFPLVSALTIVPVLLLIPAKNSYGAMLAVGFLLGLGGTTFAIGVPLVNSWFPPHKRGFALGVFGMGMGGVALSGFFTPRIAKHGDNLPFLVVAGALVVFALLAAVLVSDHPDRKIPTDTLAHRLGEAGKLRVTWELSALYAIGFGGIVAFGVYLPTYLKTWYEMSPTEAGTKAAGFALVTVVFRPVGGWLSDRIHPAVVTSVALLLAALMAIVQAFEPPLNPVGTIALLAMAAGLGTASGSVFALVSQVTPQPKVGSVTGIVGAMGGLGGFVPPLVMGAIYSAKDSYAIGFMLLSDLALAGCVYAYGRMRTVQRDE

Crispr_ID: NZ_CP010833_21

• CRISPR_ID: NZ_CP010833_21
• CRISPR_location: 5984647-5984737
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_21

Consensus_repeat	Method
CCGCGTACAGCCGGAGCCCGGCCGC	CRISPRCasFinder

spacers of NZ_CP010833_21

>21.1|5984672|41|NZ_CP010833|CRISPRCasFinder
GTACAGCCGGGGCCCCGGCCGCACGCAGTCGGTGGACCGGC

CRISPR arrays and Neighbor proteins around NZ_CP010833_21

CRISPR arrays

The CRISPR arrays of NZ_CP010833_21

>merge|NZ_CP010833|21|5984647-5984737|CRISPRCasFinder
CCGCGTACAGCCGGAGCCCGGCCGCGTACAGCCGGGGCCCCGGCCGCACGCAGTCGGTGGACCGGCCCGCGTACAGCCGGAGCCCCGGCCG

>NZ_CP010833|21|19|5984647-5984737|CRISPRCasFinder
CCGCGTACAGCCGGAGCCCGGCCGC	GTACAGCCGGGGCCCCGGCCGCACGCAGTCGGTGGACCGGC
CCGCGTACAGCCGGAGCCCCGGCCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075266785.1|5981397_5981886_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266779.1|5974759_5976910_+|regulator	unknown	unknown	gnl|CDD|226418
NZ_CP010833.1|WP_075266795.1|5993234_5993759_+|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl|CDD|225039
NZ_CP010833.1|WP_075266783.1|5979611_5980526_-|metal-dependent-hydrolase	unknown	unknown	gnl|CDD|378401
NZ_CP010833.1|WP_075266789.1|5984773_5985421_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|225107
NZ_CP010833.1|WP_075266787.1|5983555_5984101_-|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl|CDD|225039
NZ_CP010833.1|WP_075266786.1|5981919_5983479_-|DUF1996-domain-containing-protein	unknown	unknown	gnl|CDD|370451
NZ_CP010833.1|WP_075268578.1|5993787_5994747_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266792.1|5987971_5989006_-|glutamine-synthetase	unknown	unknown	gnl|CDD|177922
NZ_CP010833.1|WP_075266796.1|5994808_5995174_-|arsenate-reductase-family-protein	unknown	unknown	gnl|CDD|239332
NZ_CP010833.1|WP_075266782.1|5978510_5979608_-|oxidoreductase	unknown	unknown	gnl|CDD|99782
NZ_CP010833.1|WP_075266784.1|5980617_5981370_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|369777
NZ_CP010833.1|WP_075266780.1|5977026_5977731_+|DUF2470-domain-containing-protein	unknown	unknown	gnl|CDD|378456
NZ_CP010833.1|WP_075266788.1|5984133_5984628_+|MarR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224759
NZ_CP010833.1|WP_075266791.1|5986893_5987562_-|winged-helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|294013
NZ_CP010833.1|WP_075266794.1|5991639_5993187_-|PLP-dependent-aminotransferase-family-protein	unknown	unknown	gnl|CDD|224089
NZ_CP010833.1|WP_006123979.1|5995293_5995599_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266781.1|5977746_5978475_-|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|224228
NZ_CP010833.1|WP_075266793.1|5990768_5991683_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP010833.1|WP_075266790.1|5985405_5986674_-|sensor-histidine-kinase	unknown	unknown	gnl|CDD|226951

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075266779.1|5974759_5976910_+|regulator	gnl|CDD|226418	COG3903, COG3903, Predicted ATPase [General function prediction only].	2.03958e-37
NZ_CP010833.1|WP_075266795.1|5993234_5993759_+|carboxymuconolactone-decarboxylase-family-protein	gnl|CDD|225039	COG2128, COG2128, Uncharacterized conserved protein [Function unknown].	1.2455e-23
NZ_CP010833.1|WP_075266783.1|5979611_5980526_-|metal-dependent-hydrolase	gnl|CDD|378401	pfam10118, Metal_hydrol, Predicted metal-dependent hydrolase. Members of this family of proteins comprise various bacterial transition metal-dependent hydrolases.	7.91101e-95
NZ_CP010833.1|WP_075266789.1|5984773_5985421_-|response-regulator-transcription-factor	gnl|CDD|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	3.60314e-38
NZ_CP010833.1|WP_075266787.1|5983555_5984101_-|carboxymuconolactone-decarboxylase-family-protein	gnl|CDD|225039	COG2128, COG2128, Uncharacterized conserved protein [Function unknown].	4.16444e-10
NZ_CP010833.1|WP_075266786.1|5981919_5983479_-|DUF1996-domain-containing-protein	gnl|CDD|370451	pfam09362, DUF1996, Domain of unknown function (DUF1996). This family of proteins are functionally uncharacterized.	2.59176e-26
NZ_CP010833.1|WP_075266792.1|5987971_5989006_-|glutamine-synthetase	gnl|CDD|177922	PLN02284, PLN02284, glutamine synthetase.	6.7463e-161
NZ_CP010833.1|WP_075266796.1|5994808_5995174_-|arsenate-reductase-family-protein	gnl|CDD|239332	cd03034, ArsC_ArsC, Arsenate Reductase (ArsC) family, ArsC subfamily; arsenic reductases similar to that encoded by arsC on the R733 plasmid of Escherichia coli. E. coli ArsC catalyzes the reduction of arsenate [As(V)] to arsenite [As(III)], the first step in the detoxification of arsenic, using reducing equivalents derived from glutathione (GSH) via glutaredoxin (GRX). ArsC contains a single catalytic cysteine, within a thioredoxin fold, that forms a covalent thiolate-As(V) intermediate, which is reduced by GRX through a mixed GSH-arsenate intermediate. This family of predominantly bacterial enzymes is unrelated to two other families of arsenate reductases which show similarity to low-molecular-weight acid phosphatases and phosphotyrosyl phosphatases.	1.12957e-40
NZ_CP010833.1|WP_075266782.1|5978510_5979608_-|oxidoreductase	gnl|CDD|99782	cd06185, PDR_like, Phthalate dioxygenase reductase (PDR) is an FMN-dependent reductase that mediates electron transfer from NADH to FMN to an iron sulfur cluster. PDR has an an N-terminal ferrredoxin reductase (FNR)-like NAD(H) binding domain and a C-terminal iron-sulfur [2Fe-2S] cluster domain. Although structurally homologous to FNR, PDR binds FMN rather than FAD in it's FNR-like domain. Electron transfer between pyrimidines and iron-sulfur clusters (Rieske center [2Fe-2S]) or heme groups is mediated by flavins in respiration, photosynthesis, and oxygenase systems. Type I dioxygenase systems, including the hydroxylate phthalate system, have 2 components, a monomeric reductase consisting of a flavin and a 2Fe-2S center and a multimeric oxygenase. In contrast to other Rieske dioxygenases the ferredoxin like domain is C-, not N-terminal.	1.24979e-88
NZ_CP010833.1|WP_075266784.1|5980617_5981370_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	2.343e-20
NZ_CP010833.1|WP_075266780.1|5977026_5977731_+|DUF2470-domain-containing-protein	gnl|CDD|378456	pfam10615, DUF2470, Protein of unknown function (DUF2470). This family is a putative haem-iron utilisation family, as many members are annotated as being pyridoxamine 5'-phosphate oxidase-related, FMN-binding; however this could not be confirmed.	2.91839e-08
NZ_CP010833.1|WP_075266788.1|5984133_5984628_+|MarR-family-transcriptional-regulator	gnl|CDD|224759	COG1846, MarR, Transcriptional regulators [Transcription].	8.31132e-13
NZ_CP010833.1|WP_075266791.1|5986893_5987562_-|winged-helix-turn-helix-transcriptional-regulator	gnl|CDD|294013	cd00383, trans_reg_C, DNA-binding effector domain of two-component system response regulators. Bacteria and some eukaryotes use two-component signal transduction systems to detect and respond to changes in the environment. The systems consists of a sensor histidine kinase and a response regulator. The former autophosphorylates a histidine residue on detecting an external stimulus. The phosphate is then transferred to an invariant aspartate residue in a highly conserved receiver domain of the response regulator. Phosphorylation activates a variable effector domain of the response regulator, which triggers the cellular response. This C-terminal effector domain belongs to the winged helix-turn-helix family of transcriptional regulators and contains DNA and RNA polymerase binding sites. Several dimers or monomers bind head to tail to small tandem repeats upstream of the genes. The RNA polymerase binding sites interact with the alpha or sigma subunit of RNA polymerase.	6.79857e-34
NZ_CP010833.1|WP_075266794.1|5991639_5993187_-|PLP-dependent-aminotransferase-family-protein	gnl|CDD|224089	COG1167, ARO8, Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs [Transcription / Amino acid transport and metabolism].	9.8514e-102
NZ_CP010833.1|WP_075266781.1|5977746_5978475_-|TetR/AcrR-family-transcriptional-regulator	gnl|CDD|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.79993e-14
NZ_CP010833.1|WP_075266793.1|5990768_5991683_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	2.29952e-31
NZ_CP010833.1|WP_075266790.1|5985405_5986674_-|sensor-histidine-kinase	gnl|CDD|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	8.24841e-41

Protein sequences

>NZ_CP010833.1|WP_075266788.1|5984133_5984628_+|MarR-family-transcriptional-regulator
MVDEKKVNQVVEARKGFELPLLLFAGFRSIIDALHRDLAEHGHPETRPAYGFALQAVGRDGASISEIGRRLGVSKQAAGKTVDKLETLGYVERAPDPADGRRTLIRLTPHGVDLLTRSAEGFDRLRADWARTLGEDRLNALERDLRTMAPGGAFRLDGAGWFTG
>NZ_CP010833.1|WP_075266787.1|5983555_5984101_-|carboxymuconolactone-decarboxylase-family-protein
MPFADLTPATAPAASRRALEAVTERLGYRPAAVARLAASPHTLDGFLKISAIFDACTLDPLSREVVVMTMATRNDCHVCVAMHTAKLTALDAGPALIAALRDPGDPALPDERLEAVRRFTLAVLASAGDVDDADLRNFLAYGYTEQNALEVVLGIGAYTLSTLANRLTGAPVDEQLAAFAR
>NZ_CP010833.1|WP_075266786.1|5981919_5983479_-|DUF1996-domain-containing-protein
MRRISRKKRSTLANRAIAASAALILGGGGLVAVNVYASAGEGPSGSSPPTRTENAGSRLSTIDCPEAVNGLPEVPDEARGEVDRELAAMDTQITDAYRQFADRKEQIARDPGLAENAVLGPLRSKRTASLDRIGIAIGRAGERPAGLESLAGCSLRADDSRGGNGGGRGDGNGGDGSQDDGQGQDQGQNQGQDGGQGQDPGGQDPGQGQDPGEGQDPGQGQGQDGNGPVAADFVDIQSVQPGVDRPRQRRGASRGTFTTDCGRNENGKFNPDNVIVAPGVSNGAHHMHDYIGNQANDAFASDDDLANGATTCRNQGDRSTYYWPVLRLQNGQDEDDVNADGGGRDQNVGEIQTPSQVTLKFVGSPVGRVTAMPRFLRIITGDAKAFTNGDANANASWSCTGFEDRQLTDKYPICPEGSQVVRTFAFQNCWDGQNTDSANHRTHVAFAQENGRCPNGFRAVPQLVQRIVYDVPPGPGFAVDSFPEQLHKPITDHGDFINVFDDRLMKKMVRCINDGRRCR
>NZ_CP010833.1|WP_075266785.1|5981397_5981886_+|hypothetical-protein
MVTQPEWRDARRGGATGLVLAGFLLLAGCSTEPADDHGGRERPTPKPAATGTLEQLAKKAGCDPNVQTDAAELRQANCKTDEGRYVLTTFATDRGQREWINEAKDYGGSYLVGRQWVAVGDPEVVAALRGRLGGTVETASPHHSGNSGGGGSEDGHSGHHPG
>NZ_CP010833.1|WP_075266784.1|5980617_5981370_+|class-I-SAM-dependent-methyltransferase
MTKPVQARSFDAIAAAYDAHRPSYPPALFDAIEELAGIPLAGARVADVGAGTGLGTARLHERGARVTAVEPGDGMAEQFARSLPDVPLVRGDGNNLPLRTGSVDLITYAQAWHWTDPARSIPEARRVLRPGGALALWWNDGDPAVEWLAEQENRMRVFFGVDIPEAPDVRARFRAVLPDELDFRTRQVAWSRRVPVDAHIANMATHSDFLIGDPVAVRDFFDRERALLTALFPDGQLEEAYLVSLAVAHP
>NZ_CP010833.1|WP_075266783.1|5979611_5980526_-|metal-dependent-hydrolase
MSNTQPAAVASERTPLKARKVSFAWEKTPLHWVPGDPFTTHTINVLHLLLPAGERWFIHVYRQILPYIHDDQLREDVIGFIGQEAVHSQAHDDVLPHLRELGLDPTPYTAQVDWFFEKLLGDRTLPPGRASKWWLMERVATIAAIEHYTAFLGDWILNAEALDRKGADPTMLDLLRWHGAEEVEHRSVAFDVFMHVDGGYRRRVRTWAAAFSALVFLWQRGTRFFMENDPTLLDGKASFKAFHASGKQGTLPSTGAILRSVPSYLSRSYHPSHEGSTAQAVEYLTRSPAALAAESAESATAKGV
>NZ_CP010833.1|WP_075266782.1|5978510_5979608_-|oxidoreductase
MALPRLRTVVLVSGAALLTRRALKRRIARSPLWPLPALPEPISGHSKRRATAVRKLLIAGRTEVAEGVVQLRLEGPGLPPWSPGAHLDLVLPSGLVRQYSLCGDPADTGAYTVATRLVTDGRGGSREVHDQLQEGLEVEVRGPRNRFPLTEAPGYVFVVGGIGITPVLPMLRALAASGAEWRLLYGGRSRASMPFLEEIEKLGADGDRVTVVAQDEAGHPDVAGALADLAPGTAVYCCGPEPLMAAATAALPEGCTLHLERFSAATGSTAGSDAGSEGSEAFEVELRRSGRTVPVAAGQSVLAAVRAELPHVSYSCEQGFCGTCQQRVLEGEIDHRDELLTEDERGDSMLICVSRCRGGRLVLDL
>NZ_CP010833.1|WP_075266781.1|5977746_5978475_-|TetR/AcrR-family-transcriptional-regulator
MTTGVRRRMGVDERRQQLIGVALDLFSRRSPEDVSIDEIAAAAGISRPLVYHYFPGKQSLYEAALRRAADELAARFLEPLEGPLGARLLRVMGRFFDFVDEHGPGFSALMRGGPAAGSSTANAMIDGVRQAAYEQIITHLGVSEPPARLELVVRSWVSLAESTALIWLDGRRIPREELEMQLVHDFAALAAVSAAYDQEMAGIVLRVLSQEPADGPFGDLLARLSAFAPDVPAVPAQRLPKP
>NZ_CP010833.1|WP_075266780.1|5977026_5977731_+|DUF2470-domain-containing-protein
MRLSRPRATQPTRAERVRSILTVAHSMTVVSDGLHTEVRRLDGTGAMGHIHLHAPNDGNHAPSAERVPARLEFTDIAATPVRDRLRARVTVTGLLASPYSTDTEQSTCMEFGQAVLEDAEGRTFVTLEELEEAETDPIAACEAGMLTHLVDDHAELVPLLLRLVHPRPERGMTRAVPLAMDRYGVTLRLEYPNAHEDVRLPFPRPVTEIDQAGPQIHALLAAARRVSHRNGLPA
>NZ_CP010833.1|WP_075266779.1|5974759_5976910_+|regulator
MMTNVGYLPEETSSFVGRRAELARLHTALTTRRMTTLIGPGGVGKTRLALRAARTAAERYADGAWWADLSPLSDDRLLLPAVSDAVGLADHTLRMPVEALCEWLGDKHLLLVLDSAEHLRGPCSHLLAEILTTSPALTVLVTSRQPLGTRGEYVVEVPPLPLDGAPDALQLFADRLRATDPRAGLDAPGDEAAAAEICRRLEGIPLAIELAAAGIGRHSVAQLATRIGTRFDVPGLTVGAPGAYGSSGAAGLVGGPESSSAPGTSRLDLLADETVWPRRHRTLRTAIGWSHELCTPLERLLWARLTPLRTDFDAEVAREVCAGGPLTPDEVDRALQGLVAQSVVQRDGDRYRMLDTLREYGRMWLTELGEARAAADRHALSFLGLARRAHEGWTGPDQVSWYHKVSDTHLDLCAALEHLLAHDVEGAQEMAGRVGFFWACCGHLSEARNYAQRALDAGPVEGPHRTRLQWVLGVAALLQSDFATAEKYGALCTATALYDADDEGMLAATYLSGITQLMTGEPEAALEAARRVLRMTEGVPVDSGHRLRCRLVTVFALTALGRLAESEAAATALRRACERGGEFWTRSYVDYQLALIALLQGRPDASAAHARAMLAGKHRLRDSFGIALGLDLLAAAIAAQGAGAQAARVYGTGHAYWRMVGHPQRGTPELGPVRERCELQARAAVGDEAYQRAFERGQSDNAEVGLAAALRTELQL
>NZ_CP010833.1|WP_075266789.1|5984773_5985421_-|response-regulator-transcription-factor
MRVVLAEDLFLLRDGLVRMLEAYDFEIAAAVETGPELTQALTELKPDVAVVDVRLPPSHTDEGLQCALAARRARPGLPVLVLSQHVEQLYARELLADGNGGVGYLLKDRVFDADQFIDAVRRVAAGGTAMDPQVISQLLSRRSQDKPIGGLTPREREVMELVAQGRSNAAIAAQLVITERAVAKHTSNIFGKLDLPPSDDDNRRVLAVLAYLDRG
>NZ_CP010833.1|WP_075266790.1|5985405_5986674_-|sensor-histidine-kinase
MKAMTGRLRPSVLAAGRGLFLFVAAMTVSVTLFVLAVISISFILLGIGVFTTPVVLEAVRKHANQRRLWAMTWSDVRIPVPYRPFPKDLRSGVTGQVERTTLMLKDPATWRDMQWLLIDMTVGAVVAFVGAALMVYPVEGLVLAAGLWRVFRDDPYWYGFVPVDSQATAFAALALGIVLFHVGLWASRPLLRLHFSLARTVLAPTRDEELAQRVERLTETRHEAVDTAAAELRRIERDLHDGAQARLVAMGMNLGTIEALIEKDPAQAKKLLAMARESSAEALTELRDLVRGIHPPVLAERGLGDAVRALALRLPLASEVAVELPGRAEAPVESAAYFAVSEALTNAVKHAAAERVYVDLHHAEGMLRISVTDDGQGGAAIGSGSGLSGIERRLGTFDGVLAVSSPAGGPTMVTMEIPCELS
>NZ_CP010833.1|WP_075266791.1|5986893_5987562_-|winged-helix-turn-helix-transcriptional-regulator
MANTRTFSAASAATAASPAPAAAHPTARSVPARSLPAHQNRHRLRAVDRDEVAAPADAAGFLPPGATWLPAPPHTLPSLPGQPPMIGYLVLVPADQQPALAGAVAGAPLRPTPGTGAGATGAAGAEGVSAGPVRIDATRRTASVDGVALDLTYLEFELLAHLVAHPHRVHTRDQLVTTVWGYGHVGDGRTVDVHVARLRRKLGAEYRRSIQTVRRVGYKYTP
>NZ_CP010833.1|WP_075266792.1|5987971_5989006_-|glutamine-synthetase
MTFKAEYIWIDGTEPTAKLRSKTKIMDGAPSGDVADLPIWGFDGSSTNQAEGHASDRVLKPVFTCPDPIRGGDDILVLCEVFNIDMTPHESNTRAALRPVAEQFAGQAPIFGIEQEYTFFDGHRPLGFPEGGFPAAQGGYYCGVGADEIFGRQIVEKHLDNCLAAGLGISGINAEVMPGQWEFQVGPLSPLDVSDQLWVARWLLYRTAEDFNVSATLDPKPVKGDWNGAGAHTNFSTKAMREGYDAIITACDSLGEGSKPMDHVKNYGAGIDDRLTGLHETAPWNEYSYGVSNRGASVRIPWQVEQDRKGYIEDRRPNANVDPYVVTRLIVDTCCTALEKADQV
>NZ_CP010833.1|WP_075266793.1|5990768_5991683_+|Gfo/Idh/MocA-family-oxidoreductase
MTTADTTSPLRIGLLGTGPWARNTQAPALAAHPGVELSGVWGRRAEAAEPLAAAHGTRAYTGEEGIDALLEASDAVAFALPPDVQAPLAVRAAEAGCHLLMDKPVATTVAGARAVAEAAEKAGAASVVFCTLRFAPETAAWIAEQTAVGGWFTARAQWLGSLYAAGSASEYADSPWRREKGGLWDVGPHALSVLIPVLGEVEHLTAAAGPADTTHLILRHASGASSTVTLGLSAPPGAAGVEMELRGERGTASVPGWAGAETAFRSAVDALAEAVRTGVPHACDARFGLHLTELLVAAEEQARA
>NZ_CP010833.1|WP_075266794.1|5991639_5993187_-|PLP-dependent-aminotransferase-family-protein
MTDSWVNSAEILGSDLPLELSGTGNRRALLMDALREAVRSGRLAPGTRLPPYRSLAADLGLARNTVADAYAELVAEGWLAARQGSGTRVAERAAPVTPVHRPRTPERVARPVHDLVQGQPDPSVFPRTAWLASARRALAAAPDDAFGPGDPHGRPELRRALAGYLARVRGVRAAPDRIVLCSGAAHGLRLLAEVVGGPWAAEAYGLPFHRELLASHGVGTRPLGVDADGARVDGLTRRDRAVLLTPAHQFPTGGPLHPARRAAVVDWARSTGGLVVEDDYDGEFRYDRQPVGAVQGLDPEHVVLVGSVSKSLSPALRIGWMVLPQRLVAPVVAAKGEREPFSSATEQLTLADFIESGAYDRQVRRMRQRHRRRRDQLVAALHARAPHVRVTGIAAGLHAVVELPPGTERSAVRAAAWQGLAVEGLGDYLHPGAEHASRAPRASRAHRAGGADALRAAGPADASLVPHRDGLVVGYATPAESAYPEALEALCRSLPPAGPPATTPAPAPPPPPAAP
>NZ_CP010833.1|WP_075266795.1|5993234_5993759_+|carboxymuconolactone-decarboxylase-family-protein
MTTTEIKTNDRTTAEATTVRPNPTTAAPRLNFAKAAPKAFRAVIGLDAAAREGLDPALVELVQIRASHLNRCAYCLHMHTTDARRAGESEDRLHMVAVWQEADHFFTAREQSALALTDAVTRIGDAGVPDEVYDRAAAHFTEEELAHLLALIFTINTWNRIALSTAKRAGTDER
>NZ_CP010833.1|WP_075268578.1|5993787_5994747_-|hypothetical-protein
MAFFTDFVVTGGVRGADATSTPAEVTGLLGDAFVESRTGPGQLLRSYHLVEVAWEREQEGEDWRGLYVTVQAHRLDVPLSVDALAADLEQAGFPLVEVAPDGVGCRRFVRPDSRVAVLVDEESGQVLAMTTPAWFAPGARGEPSPWSRESGRDQVRHLVGLGAAEREAWARRRAPGEAEEAARWWWFLWVACRQLLPDEGERRFGHDRSVWEVLALWLLGSCEAAGVLDRTDAVREIVRYGLLEPDTAVRACLDAIVVSRADVATRESTPYARENLEAVNASRAAKRLALAAGELLPRVRDRALRAEVAAWLELRTRLM
>NZ_CP010833.1|WP_075266796.1|5994808_5995174_-|arsenate-reductase-family-protein
MEIWINPACSKCRSAVTLLDAEGADYTVRRYLEDVPSPDEIRAVLDRLGLEPWDITRTQEAAAKELGLKEWPRDAGSRERWIAALSEHPKLIQRPIITAGDGTAVVARSEEAVREALGRGA
>NZ_CP010833.1|WP_006123979.1|5995293_5995599_+|hypothetical-protein
MAVATATTEPLDRQLPMPFHPPLPAPPAKKRLPAGRPREWYVSHNRRLKAMRLAIALLDSGVYQPSSAGNHRIRITAERMGIHPPSDTTCRMVRALIRYGR

Crispr_ID: NZ_CP010833_22

• CRISPR_ID: NZ_CP010833_22
• CRISPR_location: 6272000-6272112
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_22

Consensus_repeat	Method
CGCCTGGTCGGGACTGCCCGGGGGCGG	CRISPRCasFinder

spacers of NZ_CP010833_22

>22.1|6272027|59|NZ_CP010833|CRISPRCasFinder
TTGAGCCGTCGCACCTCGCCTGGTCGGGACTGCCCGGGGGCGGTTGAGCCGTCACACTT

CRISPR arrays and Neighbor proteins around NZ_CP010833_22

CRISPR arrays

The CRISPR arrays of NZ_CP010833_22

>merge|NZ_CP010833|22|6272000-6272112|CRISPRCasFinder
CGCCTGGTCGGGACTGCCCGGGGGCGGTTGAGCCGTCGCACCTCGCCTGGTCGGGACTGCCCGGGGGCGGTTGAGCCGTCACACTTCGCCTGGTCGGGACTGCCCGGGGGCGG

>NZ_CP010833|22|20|6272000-6272112|CRISPRCasFinder
CGCCTGGTCGGGACTGCCCGGGGGCGG	TTGAGCCGTCGCACCTCGCCTGGTCGGGACTGCCCGGGGGCGGTTGAGCCGTCACACTT
CGCCTGGTCGGGACTGCCCGGGGGCGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075268600.1|6263117_6266138_+|DEAD/DEAH-box-helicase	unknown	unknown	gnl|CDD|223627
NZ_CP010833.1|WP_075266965.1|6273076_6274012_-|pseudouridine-5'-phosphate-glycosidase	unknown	unknown	gnl|CDD|377251
NZ_CP010833.1|WP_107472831.1|6260837_6261209_+|hypothetical-protein	unknown	unknown	gnl|CDD|238121
NZ_CP010833.1|WP_032761469.1|6281752_6282331_+|TerD-family-protein	unknown	unknown	gnl|CDD|376767
NZ_CP010833.1|WP_075266961.1|6266146_6267526_+|hypothetical-protein	unknown	unknown	gnl|CDD|226729
NZ_CP010833.1|WP_075266970.1|6279396_6281538_+|excinuclease-ABC-subunit-UvrB	unknown	unknown	gnl|CDD|235395
NZ_CP010833.1|WP_075266966.1|6276012_6276537_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266968.1|6277407_6278295_-|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl|CDD|176543
NZ_CP010833.1|WP_075266967.1|6276746_6277304_-|methylated-DNA--[protein]-cysteine-S-methyltransferase	unknown	unknown	gnl|CDD|223427
NZ_CP010833.1|WP_006123715.1|6267569_6268301_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_030814032.1|6269321_6270533_-|pyridoxal-phosphate-dependent-aminotransferase	unknown	unknown	gnl|CDD|181738
NZ_CP010833.1|WP_075266969.1|6278526_6279357_+|hypothetical-protein	unknown	unknown	gnl|CDD|225837
NZ_CP010833.1|WP_075266963.1|6270600_6271335_+|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl|CDD|224647
NZ_CP010833.1|WP_075266960.1|6262385_6262742_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266959.1|6261662_6262361_+|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl|CDD|379312
NZ_CP010833.1|WP_075268602.1|6274553_6275771_-|MFS-transporter	unknown	unknown	gnl|CDD|340883
NZ_CP010833.1|WP_079181547.1|6261205_6261559_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075266962.1|6268677_6269325_-|peptidase	unknown	unknown	gnl|CDD|379241
NZ_CP010833.1|WP_075266964.1|6272141_6273053_-|sugar-kinase	unknown	unknown	gnl|CDD|238571
NZ_CP010833.1|WP_010061239.1|6274116_6274479_+|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|368658

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075268600.1|6263117_6266138_+|DEAD/DEAH-box-helicase	gnl|CDD|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	3.44909e-122
NZ_CP010833.1|WP_107472831.1|6260837_6261209_+|hypothetical-protein	gnl|CDD|238121	cd00200, WD40, WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from its N-terminus and the WD dipeptide at its C-terminus and is 40 residues long, hence the name WD40; between GH and WD lies a conserved core; serves as a stable propeller-like platform to which proteins can bind either stably or reversibly; forms a propeller-like structure with several blades where each blade is composed of a four-stranded anti-parallel b-sheet; instances with few detectable copies are hypothesized to form larger structures by dimerization; each WD40 sequence repeat forms the first three strands of one blade and the last strand in the next blade; the last C-terminal WD40 repeat completes the blade structure of the first WD40 repeat to create the closed ring propeller-structure; residues on the top and bottom surface of the propeller are proposed to coordinate interactions with other proteins and/or small ligands; 7 copies of the repeat are present in this alignment.	8.14867e-07
NZ_CP010833.1|WP_032761469.1|6281752_6282331_+|TerD-family-protein	gnl|CDD|376767	pfam02342, TerD, TerD domain. The TerD domain is found in TerD family proteins that include the paralogous TerD, TerA, TerE, TerF and TerZ proteins It is found in a stress response operon with TerB and TerC. TerD has a maximum of two calcium-binding sites depending on the conservation of aspartates. It has various fusions to nuclease domains, RNA binding domains, ubiquitin related domains, and metal binding domains. The ter gene products lie at the centre of membrane-linked metal recognition complexes with regulatory ramifications encompassing phosphorylation-dependent signal transduction, RNA-dependent regulation, biosynthesis of nucleoside-like metabolites and DNA processing linked to novel pathways.	3.31745e-55
NZ_CP010833.1|WP_075266965.1|6273076_6274012_-|pseudouridine-5'-phosphate-glycosidase	gnl|CDD|377251	pfam04227, Indigoidine_A, Indigoidine synthase A like protein. Indigoidine is a blue pigment synthesized by Erwinia chrysanthemi implicated in pathogenicity and protection from oxidative stress. IdgA is involved in indigoidine biosynthesis, but its specific function is unknown. The recommended name for this protein is now pseudouridine-5'-phosphate glycosidase.	1.19842e-148
NZ_CP010833.1|WP_075266970.1|6279396_6281538_+|excinuclease-ABC-subunit-UvrB	gnl|CDD|235395	PRK05298, PRK05298, excinuclease ABC subunit UvrB.	0
NZ_CP010833.1|WP_075266968.1|6277407_6278295_-|glycerophosphodiester-phosphodiesterase	gnl|CDD|176543	cd08601, GDPD_SaGlpQ_like, Glycerophosphodiester phosphodiesterase domain of Staphylococcus aureus and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in uncharacterized glycerophosphodiester phosphodiesterase (GP-GDE, EC 3.1.4.46) from Staphylococcus aureus, Bacillus subtilis and similar proteins. Members in this family show very high sequence similarity to Escherichia coli periplasmic phosphodiesterase GlpQ, which catalyzes the Ca2+-dependent degradation of periplasmic glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols.	5.27809e-75
NZ_CP010833.1|WP_075266967.1|6276746_6277304_-|methylated-DNA--[protein]-cysteine-S-methyltransferase	gnl|CDD|223427	COG0350, Ada, Methylated DNA-protein cysteine methyltransferase [DNA replication, recombination, and repair].	1.29735e-42
NZ_CP010833.1|WP_030814032.1|6269321_6270533_-|pyridoxal-phosphate-dependent-aminotransferase	gnl|CDD|181738	PRK09265, PRK09265, aminotransferase AlaT; Validated.	0
NZ_CP010833.1|WP_075266961.1|6266146_6267526_+|hypothetical-protein	gnl|CDD|226729	COG4279, COG4279, Uncharacterized conserved protein [Function unknown].	7.27487e-42
NZ_CP010833.1|WP_075266963.1|6270600_6271335_+|helix-turn-helix-transcriptional-regulator	gnl|CDD|224647	COG1733, COG1733, Predicted transcriptional regulators [Transcription].	7.28497e-25
NZ_CP010833.1|WP_075266959.1|6261662_6262361_+|class-I-SAM-dependent-methyltransferase	gnl|CDD|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	4.86117e-13
NZ_CP010833.1|WP_075268602.1|6274553_6275771_-|MFS-transporter	gnl|CDD|340883	cd17325, MFS_MdtG_SLC18_like, bacterial MdtG-like and eukaryotic solute carrier 18 (SLC18) family of the Major Facilitator Superfamily of transporters. This family is composed of eukaryotic solute carrier 18 (SLC18) family transporters and related bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as multidrug resistance protein MdtG, from Bacillus subtilis such as multidrug resistance proteins 1 (Bmr1) and 2 (Bmr2), and from Staphylococcus aureus such as quinolone resistance protein NorA. The family also includes Escherichia coli arabinose efflux transporters YfcJ and YhhS. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. The SLC18 transporter family includes vesicular monoamine transporters (VAT1 and VAT2), vesicular acetylcholine transporter (VAChT), and SLC18B1, which is proposed to be a vesicular polyamine transporter (VPAT). The MdtG/SLC18 family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	6.20811e-21
NZ_CP010833.1|WP_075266969.1|6278526_6279357_+|hypothetical-protein	gnl|CDD|225837	COG3300, COG3300, MHYT domain (predicted integral membrane sensor domain) [Signal transduction mechanisms].	4.00278e-35
NZ_CP010833.1|WP_075266962.1|6268677_6269325_-|peptidase	gnl|CDD|379241	pfam13529, Peptidase_C39_2, Peptidase_C39 like family.	3.18422e-06
NZ_CP010833.1|WP_075266964.1|6272141_6273053_-|sugar-kinase	gnl|CDD|238571	cd01166, KdgK, 2-keto-3-deoxygluconate kinase (KdgK) phosphorylates 2-keto-3-deoxygluconate (KDG) to form 2-keto-3-deoxy-6-phosphogluconate (KDGP). KDG is the common intermediate product, that allows organisms to channel D-glucuronate and/or D-galacturinate into the glycolysis and therefore use polymers, like pectin and xylan as carbon sources.	9.80737e-45
NZ_CP010833.1|WP_010061239.1|6274116_6274479_+|cupin-domain-containing-protein	gnl|CDD|368658	pfam05899, Cupin_3, Protein of unknown function (DUF861). This family consists of several proteins which seem to be specific to plants and bacteria. The function of this family is unknown.	2.19487e-19

Protein sequences

>NZ_CP010833.1|WP_075266963.1|6270600_6271335_+|helix-turn-helix-transcriptional-regulator
MSRLRRMPRQQQPAARPAVPPAARPVRRRSYDQFDATARALDSVGDRWTLLIVRELLGGPRRYTDLHADLPGVSTDVLASRLKDMEQSGLALRRKLPPPSAASVYELTERGHGLLPVLTALAEWGAPALDERRPTDAVRAHWFALPLLAALTGLTREGVLEVRLDEGEFHLRVGGRAGSGLPGAEAYGAVYGYGPADRPDARIALGAEVCLLLARGGATLAETVKDGRVEVLGDSPLAAELRGE
>NZ_CP010833.1|WP_030814032.1|6269321_6270533_-|pyridoxal-phosphate-dependent-aminotransferase
MEFRQSSKLNEVCYEIRGPVIEHANALEEAGHSVLRLNTGNPALFGFEAPEEIVQDMIRMLPQAHGYTDSRGILSARRAVAQRYQSMGLTEVGVDDVFLGNGVSELISMAVQALLEDGDEVLIPAPDFPLWTAVTTLAGGKAVHYVCDEESDWNPDLADMASKITDRTKAVVIINPNNPTGAVYPREILEGILDLARRHGLMVFADEIYDQILYDGAEHHSAAVLAPDLVCLTFSGLSKTYRVAGFRSGWMVVSGPHQHARNYLEGLTMLASMRLCPNAPAQYAIQAALGGRQSIKELVAPGGRLHEQRDRAWERLNEIPGVSCVKPKGALYAFPRIDPKVHPIVDDEKFVLDLLLREKIQVVQGTGFSWPRPDHFRILTLPYADDLDAAISRIGRFLNGYRQ
>NZ_CP010833.1|WP_075266962.1|6268677_6269325_-|peptidase
MTCALCSVPVHTQFATPELVGAIVEGGLDPAEDPGWAGSGAGSPAEYARWAGHLCGMTCLRMALGGDAPSLFELRDGALKYGAYTEDADGTIRGLVYAPFAEYVSEVYGREATVHRHLDVAEIPGLLNAGRTVLASVHYGIRHPERPAPGRGGHLVLVTARTADGSGVHFHNPSGTDAGTRAAVLPLTEFERFFAGRGVSLAAAEASETGAGPEA
>NZ_CP010833.1|WP_006123715.1|6267569_6268301_+|hypothetical-protein
MAKLNQIIAVEKGVKSKAHQDLTAAHHGLQKAALLAGISRTYQPKDEEGEQLPPESTLVQVKAEDVLRDTAATLTRLFDVTATKDWANCSARADVKVEGRVLVSEVPVAYLLFLEKQLTDLNTFVRKLPVLDAAEAWVQDPSTDSWKTEPVRTLRTKKVPRNHVKAEATEKHPAQVEVYYEDIPVGYWTTVKFSGALPARRVNELLDRIEKLQQAVKFAREEANGAEVTDQRVGDAVFGYLFG
>NZ_CP010833.1|WP_075266961.1|6266146_6267526_+|hypothetical-protein
MSPRPTTGPAARPTTGPAARRSAPRARIGPDDLRRTFEAVPARTSAEGEPFAASWWGRAWVDALETLSMDEARLARGRAYADDGQVAAITVTPGRIVAYVHGSRARPYRAELRLRTFADPGWETLLDAVAARPGHLSALLAKEMPHSLARTAEEAGVRLLPAADDLDPSCTCPDHGRPCKHVAALCFQTALLLDSDPFVLLLMRGRGERELLDALARRNAEHSARERPAAPAMPSVAAGDAFAARFLPPLPAPRPVPPHPGQPPSYPDLPGARDPLGLDHLATDAVARAHALLTTGRDPLAGLTEWQDAVRLAAARPTAGLTATTRALYRELAYATGRTTTDLARAVAAWRQGEAEGLAALETPWDPPAGPFDRARPALAAAGFPRFTPWRNHLTHPAGSLQLRFGQDLRWYGYESDPGAEDWWPRAAPDPDPVSALEALLAGDAVPETAGDDDPHYVR
>NZ_CP010833.1|WP_075268600.1|6263117_6266138_+|DEAD/DEAH-box-helicase
MTEGTREGETRTADVARLLRHPAVFLPGPVPREGRVAFWDPDSGGGPQGDRDPWRADPPPERTGVPSAYADAPARPDTVPYTSARLTVVRPDDAAGPGGVRTAEVLAGLLSVADALPLLVRARQQASAHPATRCWGAAALHALHLVARGRLLPGLTADGHDAWRAGPSDAEDVAHLRAIAAALPPEGHAVPPPGSAPPRLPAPEALTGAFLDAVADTLPRTPAAAFAMGAPFAAREPQHLPHAAAWAVEVASGLDAGVRVSLRLDLSAYELFDTADTYALTADRGEAETADGPVRPEHADDPAVRPAAAAIVQVHSLADPTYVVDAAALWNGGAGEPFGPRSQVDAVLALRRAARVWAPLERLLGQPVPDVLAITEDELYELLSDAGARLAAAGVEVRWPRELARSLTAAAVVRPAPGSATDGTSFFDAEHLFAFDWQLSLGDERLTEAEMDLLAEAHRPVVRLRDQWVVVDPALVRKARKRELGLLDPVDALAVALTGSAEVDGERVDAVPAGALAALRTRLLADDTTIAPPPGLDATLRDYQLRGLAWLDRMTSLGLGGCLADDMGLGKTITLIALHLHRAHPSPTLVVCPASLLGNWHREINRFAPGVPVRRFHGTDRSLSDPDGGFVLTTYGTMRSSAAQLAEQSWGLVVADEAQHVKNPHSSTAKALRTIPAPARVALTGTPVENNLSELWALLDWTTPGLLGTLKAFRARHARIVENTDTAAGLGNEEAVERLSRLVRPFLLRRKKSDPGIAPELPPKTETDHPVPLTREQATLYEAAVRETMAQIEGAEGIARRGLIMKLLTSLKQICNHPAQYLKEEPTRLTGRSGKLALLDELLDTILSEDGSVLIFTQYVSMARLLSAHLASRAIPSQLLHGGTPVPERERMVDRFQSAEVPVFLLSLKAAGTGLNLTRAAHVVHFDRWWNPAVEEQATDRAYRIGQTQPVQVHRIITEGTVEDRIAELLESKRALADAVLGSGESALTELSDRDLADLVSLRRPA
>NZ_CP010833.1|WP_075266960.1|6262385_6262742_-|hypothetical-protein
MSVTATVPRRRRRLALAAGASLLALAATGCSGLGRTAVGPVTYTTEREAVIQVNSPSVRGCHRIAPAGAHEVENGTLVDVILYRTLDCTGRGTTYVPTRFSDVTAPGSGPWRSYSFVH
>NZ_CP010833.1|WP_075266959.1|6261662_6262361_+|class-I-SAM-dependent-methyltransferase
MGESLVREGYAGTGPGAITPDGCAVELYRRLAVGEEPDVIAGVAPEGASLLELGCGAGRVTHPLVERGFRVTAVDESPEMLAEIVGARTVRSPIESLDLGDERFDVVLLGSFLVHAGEHRVRDGMLRVCRAHVRDDGIVLVQREGVAHRSELPWERTDPSGCLVRIVSADPVGGGVRSVRAEYHFDDARWTQTFLSRELSDEDLAGHLAAAGLTVDRTLTDDGTWLLARPAL
>NZ_CP010833.1|WP_079181547.1|6261205_6261559_-|hypothetical-protein
MLESEVIAMRTGSEPVTARSPLRMRLWLSLWGTAWALFGLVAFSMNGRPGWAAACAVVLLLAVVDLGVITYRMRQGPHYQPGRDVPPYEPDHGDGRPRGPGPGTDGGRPGRGRNGAL
>NZ_CP010833.1|WP_107472831.1|6260837_6261209_+|hypothetical-protein
MWSVEFSPDGKTLAAGGHTGNGTIHLWNVTDPDRPTAIGRPLTVETGFVAVLAFSPDSRTLVATPDDGVATLCDLDAESSTNRICAASSGAPGRGGRETVRRRTALRSALRSALSESSEAKKS
>NZ_CP010833.1|WP_075266964.1|6272141_6273053_-|sugar-kinase
MNRPAAGGGLLVVGEVVTDVVARYGSALAHGTDTSARIRTLPGGAGANVACWAVRSGCADVRLLARAGAGSADWHREALERAGVRAFLAVDEEAPTATVIALVDAAAERTFLSDAGAVLRLASHDFAPSMLEGVGRLHLSGYLLFAPASRAAALLAVRTAVERGVPVSVDPASAGFLGELGPKRFLEFAEGAELLLPNADEARLLTGLPEPDVAAVELSRWFPRVVVTLGARGAVVAAGGEVIGRVPGAAVREPVDSTGAGDAFTGGFLAALLAGADEVTAAAEGCRAGAVAVATVGGRPPVR
>NZ_CP010833.1|WP_075266965.1|6273076_6274012_-|pseudouridine-5'-phosphate-glycosidase
MPQNSPEPYEPVLSAEVRAALSAGLPVVALESTIIAHGLPRPRNLTVARELEGLVRSAGAVPATVAVLDGRAHVGLGEDQLERVAGDTAVRKLGHRDLAPALATGASGATTVSATAFLAARAGVGVFATGGLGGVHREWAAAQDESADLRLLARTGITVVCAGVKSILDVPATLQRLETLGVCVVGYGAKHFPGFYLSSSGEPVDWTVHSPDEVVEVIRAKEALGGPASALIVANPVAEADQLDPALHDRVLAEALDACRERGISGQGVTPFLLDQLMRRTGGASLEANLAAVRGNVTLAARIAVAAAEAE
>NZ_CP010833.1|WP_010061239.1|6274116_6274479_+|cupin-domain-containing-protein
MTTNDQVPASFAVHIPDAELVPEPLDPAQIVSGDPVVTGKVLGESPDGKQIRGIWQITPGVVTDTEANELFVVVSGRATVAVEGGATLEIGPGDACVLREGDRTTWTVHETLRKAYHISL
>NZ_CP010833.1|WP_075268602.1|6274553_6275771_-|MFS-transporter
MLVVSQILGGLGVAIGIALAPMLAAEVSGSEALSGLAPTASVLGTALLSLPLAALMASRGRRSGLMLAYLIGALGGGLVVLATMLPSFPLLLLGMAGFGAGSLAGLQARFAAADLVGPERRGRAISTVVWATTIGSVLGPNISAPASRLFRGTPVPEAAGPFLCSAAVFLLAGLVVAFALRPDPLLTARALAPGGPEGPPKRSLRAGIEAVRASPMARLALVTVTVSHTAMVSIMVMTPVDLSRHGAGLQLIGLVISGHIAGMYAFSPVMGWLADRFGRLTVIGLAVGLLSCAALLAGTAGPRHGQTAAGLFVLGLGWSAGMIAGSALLTDAVPRAAQAAVQGLSDLTMSAAAGVGGATAGVIVAQWGYGPLNAIGAALLLPVAALALRRSLRQRPGAGPGAVGG
>NZ_CP010833.1|WP_075266966.1|6276012_6276537_+|hypothetical-protein
MLNIGFTPDGDRDVPAGAERAWREGRIGLATLSATDLRYGWFAYRTDFEVGGHAFLAGAREPLVDTMFTLAHTLRGLYANGSAEIDFTESSYVIRLEVTGDRVTFTASHRAPAEPPRCAVEEYTAAVRAFVATGTAWLAGNRPAIAENPALHELRALVSDPAGGGTGDPGRRTL
>NZ_CP010833.1|WP_075266967.1|6276746_6277304_-|methylated-DNA--[protein]-cysteine-S-methyltransferase
MNSYGVGGEPAVEWDVVDSGIGPLLLAATATGLVTVAFHARPAVRDAALDRLRTRFGTEPVAAPGSARLAEPIRELAAYFAGEPRDLDLALDWSLTSGFHREVLRELASGVTYGTVVGYGELAARVGRPEGAQAVGAAMGANPLPVVVPCHRVVESDGGLGGFSGGLETKRQLLALEGVLPQPLF
>NZ_CP010833.1|WP_075266968.1|6277407_6278295_-|glycerophosphodiester-phosphodiesterase
MFVRTATASTTAAALLGAGALLLPADRPEAPDQVSAQRANPVVVAHRGASGYAPENTLAAVDAADALGIDWVENDVHRSRDGVLVVLHDTDLKRTTDVEEVFPDRAPWAVKDFTAAELAKLDAGSWFGEQFTGARIPTLTQFLHRLERNRQKLLLEIKSPATYPGIERDIIRTLGRSGWLDRSHVRDRLVIQSFGADSVKKVHELRPDITTGFLGTPAVADLPSYAAFTDQINPSYATIGADYVAAVQRLKGPHGKRLRVNTWTVNKAADAVKARGYGVDGIITNFPDVVRDATS
>NZ_CP010833.1|WP_075266969.1|6278526_6279357_+|hypothetical-protein
MQGTVDGFTHGLVTPVAAFFMAALGAALGLRCTARSLHTTRSCRIGWLALGSLSIGSGVWTMHFIAMTGFTVREAPISYDKTLTFAGLAVAVVMIGIGIFIVGYRGATRMALITGGTITGLGIASMHYLGMAGMRMAAHLAYDTPLVVLSVLIAGVASTGALWAAVTLRGALSGLGASILMAVAVTGMHYTGMAALDVHLHLPPTLPADLADVLPRDRPAEIIGPMLAGPACFLLLAAVVLLFDPRVMTGEPDPYPRVGHRPRSMVREGAARARYR
>NZ_CP010833.1|WP_075266970.1|6279396_6281538_+|excinuclease-ABC-subunit-UvrB
MRPVSKIERSVRPFEVVSPYQPSGDQPTAIAELERRIRADEKDVVLLGATGTGKSATTAWMIEKLQRPTLVMAPNKTLAAQLANEFRELLPNNAVEYFVSYYDYYQPEAYVPQSDTYIEKDSSINEEVERLRHSATNSLLTRRDVVVVASVSCIYGLGTPQEYVDRMVQLKVGEEIDRDQLLRRFVEMQYTRNDLAFTRGTFRVRGDTIEIFPVYEELAVRIEMFGDEIENLSTLHPLTGEIISEDPTVHVFPASHYVAGPERMERAVSGIEQELEQRLAELEKQGKMLEAQRLRMRTTYDIEMLRQIGTCSGVENYSMHFDDRAPGTAPNTLLDYFPDDFLLVLDESHVTVPQIGAMYEGDASRKRTLVDHGFRLPSAMDNRPLKWEEFLKRIDQTVYLSATPGKYELSRGDGFVEQIIRPTGLVDPEVVVKPTEGQIDDLVHEIRERTERDERVLVTTLTKKMAEDLTDYFLELGIQVRYLHSDVDTLRRIELLRELRSGEYDVLVGINLLREGLDLPEVSLVAILDADKQGFLRSGTSLIQTIGRAARNVSGQVHMYADKVTPAMEQAIDETNRRREKQIAYNTERGIDPQPLRKKINDIVATIAREEIDTEQLLGTGYRQGKETKAPVPALGGKAAKGGTKGAAKGRAAKAGAVTGDRPATELAGIIEEMTDRMRAAAADLQFEVAARLRDEVGELKKELRQMKEAGMA
>NZ_CP010833.1|WP_032761469.1|6281752_6282331_+|TerD-family-protein
MTVNMTKGQAISLEKSDGGTLTAVRMGLGWQAAPRRGLFGSRTREVDLDASAVLFADKQPVDVVFFRHLVSDDGSVKHTGDNLVGGAGSGGDDEAILVDLQRVPVHIDQIVFTVNSFTGQTFQEVQNAFCRIVDETNGQELARYTLDGGGQYTAQIMAKVHRAGSGWKMTALGNPANGRTFQDLMPSILPHL

Crispr_ID: NZ_CP010833_23

• CRISPR_ID: NZ_CP010833_23
• CRISPR_location: 6773805-6773879
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP010833_23

Consensus_repeat	Method
CCAGCCCCTCCGGCGCTTGAGGA	CRISPRCasFinder

spacers of NZ_CP010833_23

>23.1|6773828|29|NZ_CP010833|CRISPRCasFinder
GCGGGGCCCGGGGCGGAGGCCCCGAAAAC

CRISPR arrays and Neighbor proteins around NZ_CP010833_23

CRISPR arrays

The CRISPR arrays of NZ_CP010833_23

>merge|NZ_CP010833|23|6773805-6773879|CRISPRCasFinder
CCAGCCCCTCCGGCGCTTGAGGAGCGGGGCCCGGGGCGGAGGCCCCGAAAACCCAGCCCGTCCGGCGCTTGAGGA

>NZ_CP010833|23|21|6773805-6773879|CRISPRCasFinder
CCAGCCCCTCCGGCGCTTGAGGA	GCGGGGCCCGGGGCGGAGGCCCCGAAAAC
CCAGCCCGTCCGGCGCTTGAGGA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP010833.1|WP_075267271.1|6774091_6775384_+|uroporphyrinogen-III-C-methyltransferase	unknown	unknown	gnl|CDD|381169
NZ_CP010833.1|WP_032768095.1|6775474_6776293_+|RNA-methyltransferase	unknown	unknown	gnl|CDD|223640
NZ_CP010833.1|WP_030799984.1|6765967_6766639_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224922
NZ_CP010833.1|WP_032775521.1|6763485_6763926_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_003970287.1|6763927_6764287_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075268632.1|6780950_6781988_+|chloride-transporter	unknown	unknown	gnl|CDD|130883
NZ_CP010833.1|WP_075267273.1|6778806_6779826_+|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl|CDD|366736
NZ_CP010833.1|WP_010057250.1|6778345_6778552_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP010833.1|WP_075267274.1|6779891_6780188_+|zf-TFIIB-domain-containing-protein	unknown	unknown	gnl|CDD|379195
NZ_CP010833.1|WP_075267266.1|6764891_6765971_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|236863
NZ_CP010833.1|WP_075267277.1|6783742_6784261_-|DsbA-family-protein	unknown	unknown	gnl|CDD|372611
NZ_CP010833.1|WP_075267265.1|6762914_6763418_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379228
NZ_CP010833.1|WP_075267270.1|6770112_6773733_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase	unknown	unknown	gnl|CDD|376752
NZ_CP010833.1|WP_075267272.1|6776329_6777733_-|protein-kinase	unknown	unknown	gnl|CDD|270916
NZ_CP010833.1|WP_075267276.1|6782849_6783689_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP010833.1|WP_075267269.1|6768541_6769780_+|precorrin-6y-C5,15-methyltransferase-(decarboxylating)-subunit-CbiE	unknown	unknown	gnl|CDD|381171
NZ_CP010833.1|WP_075267268.1|6767690_6768377_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|379112
NZ_CP010833.1|WP_075267267.1|6766721_6767588_+|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl|CDD|270315
NZ_CP010833.1|WP_075267275.1|6781987_6782809_+|aminodeoxychorismate-lyase	unknown	unknown	gnl|CDD|238800
NZ_CP010833.1|WP_075267264.1|6762322_6762868_+|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|274357

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP010833.1|WP_075267271.1|6774091_6775384_+|uroporphyrinogen-III-C-methyltransferase	gnl|CDD|381169	cd11642, SUMT, Uroporphyrin-III C-methyltransferase (also known as S-Adenosyl-L-methionine:uroporphyrinogen III methyltransferase, SUMT). SUMT is an enzyme of the cobalamin and siroheme biosynthetic pathway. It catalyzes the first of three steps leading to the formation of siroheme from uroporphyrinogen III; it transfers two methyl groups from S-adenosyl-L-methionine to the C-2 and C-7 atoms of uroporphyrinogen III to yield precorrin-2 via the intermediate formation of precorrin-1. Precorrin-2 is also a precursor for the biosynthesis of vitamin B12, coenzyme F430, siroheme and heme d1. This family includes proteins in which the SUMT domain is fused to other functional domains, such as to a uroporphyrinogen-III synthase domain to form bifunctional uroporphyrinogen-III methylase/uroporphyrinogen-III synthase, or to a dual function dehydrogenase-chelatase domain, as in the case of the multifunctional S-adenosyl-L-methionine (SAM)-dependent bismethyltransferase/dehydrogenase/ferrochelatase CysG, which catalyzes all three steps that transform uroporphyrinogen III into siroheme.	6.24546e-105
NZ_CP010833.1|WP_075267274.1|6779891_6780188_+|zf-TFIIB-domain-containing-protein	gnl|CDD|379195	pfam13453, zf-TFIIB, Transcription factor zinc-finger.	1.05965e-15
NZ_CP010833.1|WP_030799984.1|6765967_6766639_+|ABC-transporter-permease	gnl|CDD|224922	COG2011, AbcD, ABC-type metal ion transport system, permease component [Inorganic ion transport and metabolism].	3.64905e-93
NZ_CP010833.1|WP_075268632.1|6780950_6781988_+|chloride-transporter	gnl|CDD|130883	TIGR01824, Anthranilate_synthase_component_I-like_protein, aminodeoxychorismate synthase, component I, clade 2. This clade of sequences is more closely related to TrpE (anthranilate synthase, TIGR00564/TIGR01820/TIGR00565) than to the better characterized group of PabB enzymes (TIGR00553/TIGR01823). This clade includes one characterized enzyme from Lactococcus and the conserved function across the clade is supported by these pieces of evidence: 1) all genomes with a member in this clade also have a separate TrpE gene, 2) none of these genomes contain an aparrent PabB from any of the other PabB clades, 3) none of these sequences are found in a region of the genome in association with other Trp biosynthesis genes, 4) all of these genomes aparrently contain most if not all of the steps of the folate biosynthetic pathway (for which PABA is a precursor). Many of the sequences hit by this model are annotated as TrpE enzymes, however, we believe that all members of this clade are, in fact, PabB. The sequences from Bacillus halodurans and subtilus which score below the trusted cutoff for this model are also likely to be PabB enzymes, but are too closely related to TrpE to be separated at this time.	6.33555e-114
NZ_CP010833.1|WP_075267264.1|6762322_6762868_+|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	3.61681e-16
NZ_CP010833.1|WP_075267273.1|6778806_6779826_+|aminoglycoside-phosphotransferase-family-protein	gnl|CDD|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	3.41055e-08
NZ_CP010833.1|WP_075267266.1|6764891_6765971_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|236863	PRK11153, metN, DL-methionine transporter ATP-binding subunit; Provisional.	4.39161e-165
NZ_CP010833.1|WP_075267268.1|6767690_6768377_+|GNAT-family-N-acetyltransferase	gnl|CDD|379112	pfam13302, Acetyltransf_3, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	9.04879e-27
NZ_CP010833.1|WP_075267277.1|6783742_6784261_-|DsbA-family-protein	gnl|CDD|372611	pfam13462, Thioredoxin_4, Thioredoxin.	1.42135e-26
NZ_CP010833.1|WP_075267265.1|6762914_6763418_+|GNAT-family-N-acetyltransferase	gnl|CDD|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	3.78892e-11
NZ_CP010833.1|WP_075267270.1|6770112_6773733_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase	gnl|CDD|376752	pfam02277, DBI_PRT, Phosphoribosyltransferase. This family of proteins represent the nicotinate-nucleotide- dimethylbenzimidazole phosphoribosyltransferase (NN:DBI PRT) enzymes involved in dimethylbenzimidazole synthesis. This function is essential to de novo cobalamin (vitamin B12) production in bacteria. Nicotinate mononucleotide (NaMN):5,6-dimethylbenzimidazole (DMB) phosphoribosyltransferase (CobT) from Salmonella enterica plays a central role in the synthesis of alpha-ribazole-5'-phosphate, an intermediate for the lower ligand of cobalamin.	1.07732e-155
NZ_CP010833.1|WP_075267272.1|6776329_6777733_-|protein-kinase	gnl|CDD|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	7.69063e-87
NZ_CP010833.1|WP_075267276.1|6782849_6783689_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	4.2361e-13
NZ_CP010833.1|WP_075267269.1|6768541_6769780_+|precorrin-6y-C5,15-methyltransferase-(decarboxylating)-subunit-CbiE	gnl|CDD|381171	cd11644, Precorrin-6Y-MT, Precorrin-6Y methyltransferase (also named CbiE). CbiE (precorrin-6Y methyltransferase, also known as cobalt-precorrin-7 C(5)-methyltransferase, also known as cobalt-precorrin-6Y C(5)-methyltransferase) catalyzes the methylation of C-5 in cobalt-precorrin-7 to form cobalt-precorrin-8. It participates in the pathway toward the biosynthesis of cobalamin (vitamin B12). There are two distinct cobalamin biosynthetic pathways in bacteria. The aerobic pathway requires oxygen, and cobalt is inserted late in the pathway; the anaerobic pathway does not require oxygen, and cobalt insertion is the first committed step towards cobalamin synthesis. CbiE functions in the anaerobic pathway, it is a subunit of precorrin-6Y C5,15-methyltransferase, a bifunctional enzyme: cobalt-precorrin-7 C(5)-methyltransferase (CbiE)/cobalt-precorrin-6B C(15)-methyltransferase (decarboxylating) (CbiT), that catalyzes two methylations (at C-5 and C-15) in precorrin-6Y, as well as the decarboxylation of the acetate side chain located in ring C, in order to generate precorrin-8X. CbiE and CbiT can be found fused (CbiET, also called CobL), or on separate protein chains (CbiE and CbiT). In the aerobic pathway, a single enzyme called CobL catalyzes the methylations at C-5 and C-15, and the decarboxylation of the C-12 acetate side chain of precorrin-6B.	2.11712e-48
NZ_CP010833.1|WP_032768095.1|6775474_6776293_+|RNA-methyltransferase	gnl|CDD|223640	COG0566, SpoU, rRNA methylases [Translation, ribosomal structure and biogenesis].	1.12837e-57
NZ_CP010833.1|WP_075267267.1|6766721_6767588_+|ABC-transporter-substrate-binding-protein	gnl|CDD|270315	cd13597, PBP2_lipoprotein_Tp32, The substrate-binding domain of the 32-kilodalton lipoprotein (Tp32) from Treponema pallidum binds L-methionine; the type 2 periplasmic-binding protein fold. This group includes the lipoprotein Tp32, a periplasmic component of a methionine uptake transporter system, and its closely related homologs. The Tp32 has both structural and sequential homology to the MetQ family of substrate-binding protein, and thus it belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea.	7.78919e-123
NZ_CP010833.1|WP_075267275.1|6781987_6782809_+|aminodeoxychorismate-lyase	gnl|CDD|238800	cd01559, ADCL_like, ADCL_like: 4-Amino-4-deoxychorismate lyase: is a member of the fold-type IV of PLP dependent enzymes that converts 4-amino-4-deoxychorismate (ADC) to p-aminobenzoate and pyruvate. Based on the information available from the crystal structure, most members of this subgroup are likely to function as dimers. The enzyme from E.Coli, the structure of which is available, is a homodimer that is folded into a small and a larger domain. The coenzyme pyridoxal 5; -phosphate resides at the interface of the two domains that is linked by a flexible loop. Members of this subgroup are found in Eukaryotes and bacteria.	7.30013e-76

Protein sequences

>NZ_CP010833.1|WP_075267270.1|6770112_6773733_+|nicotinate-nucleotide--dimethylbenzimidazole-phosphoribosyltransferase
MTDTGQIPGEGLPENAGMVEQPGIPAPDAHTFLDPSEHTPEDDDLLLMPTSQGAWSDPQAAPAPAQQGQPLAQTATAQPPVADHGPAQPQPQVPAQQFQEAPAAETPSTHETGGRDSGSVDLNGVRIPAPAPAPVGAHTAPAPARRPLHRGPAAADPPSYGGGTQGGVVRSLADRGPAGATRTAPPARHAGPPTTGPEYFDIPAEDPSTLPGPQLGEIPPQAGAPWGTQPEQPVAEPVAVEPVAAEQTAAEPVQQPEQVAVEPEQAVTAEQPVTEPVVAEQAEAVAEQPVQAEQAEAAAEQPVRTAPPVQPAEQAPVPAPEEVLVAPVAPAVPAAPVEQSAQPDQLVQSAAGVQPEPAPQAVPAETVVPEPVAVAMPPAGPVLVPEPVEAQPETPAEPAEAPAQAAQETPEPVEAQQVVAVAPEPEAEAVPVAAVAPEPQALVQEPPVVEPVAQPEPVVQPEQMAQPDQEQPVEPAPAAVVAESPEAAVPAAAATEEQLAAPLAPEPVQLEPVQPEPVAEEPVDQPVEAAEPVTEGTAGGNAPQQEAAPVPAPEPTVEPAVTATEPEAAHVLAPDAEDGTGPEVIETPELLPEPPATEAQPTEPQQAEAPQPEELPEPAEAVEAAEQPATPPAPGYDDAEREAVLRVMRERRDIRNGFRSDPIPHEVLLRVLEAAHTAPSVGHSQPWDFVVIRSAETRRSMHELAQSQRDAYAKSLPKGRAKQFKELKIEAILDTPVNIVVTADPTRGGRHTLGRHTQPQMAPYSSALAVENLWLAARAEGLGVGWVSFFDEREMVRALGLPEHLEVVAYLCVGYVDEFPEEPELMQAGWSKRRPLSWVVHEETYGRRALPGAEPHDLLQETISAIRPLDAKALGEAWERQKRMTKPAGALGMLEIISAQLSGLSRMCPPPIPEPAAVAIFAGDHGVHAQGVTAWPQEVTAQMVANFLGGGAVCNAFAAQVGAEVCVVDVGVATDLPATPGLLPRKVRPGTADFTTGPALTREEVLAAIEVGIETARDLVAAGNKALLTGEMGIANTTASAALICVYTGIDAAEVTGRGTGINDEMHARKVDVVRRALDLHQPDPADPIGVLAAVGGLEHAAMAGFLLGGASLRTPVILDGVSAGAAALVARAIAPEALAACIAGHRSAEPGHVAALNKLGLRPLVDLDLRLGEGTGALLALPIVQSAARAMHEVATFDSAGVTEK
>NZ_CP010833.1|WP_075267269.1|6768541_6769780_+|precorrin-6y-C5,15-methyltransferase-(decarboxylating)-subunit-CbiE
MADRVTVIGWDGSPLPGAATAALSAATLVAGAAHHLALPEVPPNAERIRLGSVDLAARRIAGHRGSAVVLADGDPGFFGVVRTLRAREHGLEVEVVPAVSSVATAFARAGMPWDDAQIVVAHPRTLRRAVNVCRAHHKVAVLTSPGAGPAELALLLDGIHRTFVICEELGTDRERVTVLTSDKAADHAWRDPNVVIVIGSGPETTAVGAWIAGRRPAYPQGIRGWALPAEAYRAAGAERMQESGEGEFPGLRAAQLARLGPRTGDLLWDIGSGSGALAVEAARFGAAVLAVDADPAACARTEAAARAFGVPVQVVRGSAPHVLERLPEPDVVRIGGGGVPVARAVVDRRPERIVTHASNRDEAEALGAALTGNGYTVECSLLQSVDLDTEVWTERERSVVFLLSAGRSDLAP
>NZ_CP010833.1|WP_075267268.1|6767690_6768377_+|GNAT-family-N-acetyltransferase
MLCFYPVLGMELRMTTTFPSISISTDRLVMRPFEMADIPAYIEMMNDETVVAWMDGPNPYTQVDAERWVRRIAPAERTGGQGIALAVTEFLTQRLVGSVRLLNTDWRTRSTEVRYITAPWARGEGYATESVLAIAEWLFRDQGFERIELRTPADNTASQQVAQKLGCISEGVLRNARIARIRTENGTDGGWTEIRTDLIVWGLLPEDLEGVAEQLADAGGYGTYNDWK
>NZ_CP010833.1|WP_075267267.1|6766721_6767588_+|ABC-transporter-substrate-binding-protein
MRKNIKITAAAAATAALAIGLSACGTSSDPASKSETGANADTSKALVVAASPTPHADILNFVKKNLADKEGLKLEVKEFTDYVLPNTATQNGQVDANFFQHKPYLDDFNAKQKTTIVPVVDVHLEPLGLYSNKVKDLKDIKAGQTIAVPNDTTNGGRALQLLAENGLITLKDGVGTSAKLSDITDKKGLEFKELEAATVPRALNDVDAAVINGNYAIEAKLKPGKDSIVLEKAEGNPYANFLAVKEGNEKDPRVEKLAKLLNSDEVKKFIEDTYQGSIVPAFGAPAKS
>NZ_CP010833.1|WP_030799984.1|6765967_6766639_+|ABC-transporter-permease
MTWSEMQPLLTQGTYDTLYMVLWSALVTVVGGLPLGVLLVLTDKGGLLQNTVVNKVIGVIVNIGRSLPFIILLIALIPFTTWVVGTFIGPTAMIVPLAVGAIPFFARLVETAIREVDHGLVEAVQSMGGSIPTIVRKVLLPQALPSLVSGVTTTLIVLIGYSAMAGAVGGEGLGSKAVTYGFQRFDNQFMLITVALLIVIVTVIQLIGDLTVRLLARRGRTAS
>NZ_CP010833.1|WP_075267266.1|6764891_6765971_+|ATP-binding-cassette-domain-containing-protein
MITTTGLTKVYQSRDREVTALDGVDLHVREGEVYGVIGQSGAGKSSLIRCVNLLERPTSGTVTVAGQDLTALAGRGRRASAELRRARTRIGMVFQHFNLLDSRTVLDNIELPLEILGVSGQARTRKAKELLDLVGLADKAKSYPGQLSGGQKQRVGIARALAGDPQVLLSDEATSALDPETTRSILQLLRDLNQQLGLTVLLITHEMDVVKTICDSAALMQRGRIVESGTVGELLATPGSELAQELFPVGGTASGPDRTVVDVTFQGESASQPVISQLSRTYNIDISILGAAMDTVGGKQIGRMRIELPGRFEENVVPIGFLREQGLQAEVVDGESTATAAAPPVPEQTPAAITKEAVK
>NZ_CP010833.1|WP_003970287.1|6763927_6764287_-|hypothetical-protein
MLDALTVAVAVTALALAAWCGHAAYRDQPTKDWHFIGMAVVSVLALAQLVVGVVQLARGERPEQGMAVFIAYLIGSFAAVPAAGFLSLTERTRWGSVTVAAGAVVLAVLEVRLYDIWGN
>NZ_CP010833.1|WP_032775521.1|6763485_6763926_-|hypothetical-protein
MSDTDRPEVAAAPKPAFELGTGPGRVLVWFYGVFTVAAASRSIVQMIMDFDRAPLAYVLSAVAAVVYGFITYSLVRGGEKARRAALVCCAAELLGVLVVGAWTLAEPAAFPDATVWSDFGMGYLFIPVILPVTGMIWLRRAKTVAV
>NZ_CP010833.1|WP_075267265.1|6762914_6763418_+|GNAT-family-N-acetyltransferase
MGMSVTISAATAQDVEQIFRLQYLCFQREAELYDNYRIDPLVQSLDSLRAEVADDLVFVARLGDEVIGAVRGFTDPDGTGLIGKLCVHPRLQGHGLGARLLLAAESALTTERSATRFRLHSGHRSESNLRLYRKAGYAQVGAVTGADGVRLILLEKDAAERDFVASA
>NZ_CP010833.1|WP_075267264.1|6762322_6762868_+|sigma-70-family-RNA-polymerase-sigma-factor
MTLLDHDLGPASSAALVVRALQPLVRAEARAEAPAAGVDPADLEQSVWVRLLERPAAAGPPADAARWVRDTVRSEVRRARRTARRERPYAGTEPAAGPADCPERAALGAAERRALRTAMARLPGRCPRLLEALLDPGDPTYREIAGELGMSQGSLGPIRSRCLGCLRRMLAAEVVAPSVRG
>NZ_CP010833.1|WP_075267271.1|6774091_6775384_+|uroporphyrinogen-III-C-methyltransferase
MAEHADHADRSGHADHPAYPVGLRLHGRRVVVVGGGQVAQRRLPQLIATGAVITLISPSATPSVEAMADAGEIRWERRRYQDGDLADTWYALVASSDTPANDAASAEAERTRTWCVRSDDAEAATAWTPATGRIENITVAVLNTTPRGRDPRHSAALRDAIVEGLRDGSIAAPHHRTRAPGVALVGGGPGDPDLITVRGRRLLAEADVVIADRLGPRDLLDELPPHVEVIDAAKIPYGRFMAQEAINQALIEHAKAGKSVVRLKGGDPFVFGRGMEEAQALAAEGIPCTVVPGISSTISVPGAAGIPVTHRGVAHEFTVVSGHVAPEDPRSLVDWEAIARLRGTLVLLMAVDKIGAIAAALIAHGKDPATPVALVQEGTTAAQRRVDATLADVGERAVAEDVRPPAVIVIGDVVAVGPDSAPAPVQDAAE
>NZ_CP010833.1|WP_032768095.1|6775474_6776293_+|RNA-methyltransferase
MAELITVDDPDDPRLSDYIGLTDVELRRRREPAEGLFIAEGEKVIRRARQTGYEMRSMLLSAKWVDVMRDVIDEVPAPVYAVAPELAERVTGYHVHRGALASMQRKPLPAADELLTTARRVVVMESVNDHTNIGAIFRSAAALGMDAVLLSPDCADPLYRRSVKVSMGAVFSVPYARLEAWPKGLEAVREAGFRLLALTPDAKATSIDEAAPHRLERVALMLGAEGDGLSTRALMAADEWVRIPMAHGVDSLNVGAAAAVAFYAVATGRPES
>NZ_CP010833.1|WP_075267272.1|6776329_6777733_-|protein-kinase
MAMMRLRREDPRLVGSFRLHRRLGAGGMGVVYLGSDRRGQRVALKVIRPDLAEDQEFRSRFAREVSAARRIRGGCTARLVAADLEADRPWFATQYVPGPSLHDKVAEEGPLAAAEVASIGAALSEGLVAVHEAGVVHRDLKPSNILLSPKGPRIIDFGIAWATGASTLTHVGTAVGSPGFLAPEQVRGAAVTPATDVFSLGATLAYAAMADSPFGHGSSEVMLYRVVHEEAQLRGVHDALAPLISACLAKDPEERPSTLQLSMRLKEIAAREAQGLHESRPPAQRSAQDANRPTGRMADPYADQDTRRSEGPSGSRPQPGRRAAPVRSGPPRTGGSRPQQASRNTTRSGGKTGQRQGAPAGTNGRPGTRSGGRTTSAGRRPANPRLLRQRLVVFVVVTLLVALGIAVAQGCQGPARGLGGSERPGGVSRAQAWTGADSAPDDSGAGPGIASRAGAGAGSAVPAGPAS
>NZ_CP010833.1|WP_010057250.1|6778345_6778552_+|hypothetical-protein
MADTATRTVVRMRGRKAYASFGARPSGTRHPLVATAMVLPLAALLVVVFGGWEAVVTQASSVAVMLGR
>NZ_CP010833.1|WP_075267273.1|6778806_6779826_+|aminoglycoside-phosphotransferase-family-protein
MTTTQTSVVHDLGTLAHRLSHPARTPCVCEPPQVLADRPDGTVVRSGAIVAKAHAADTDRAALTARIALAAAPQLAGILLPPLTAPEPAAPTARPVTLWPLGAPVDPTDPGAAPWAEAADLLARLHRTEPPFPLPPMRGPAKAARAVARMRAALRGDAITPPRDPAVEPGDAPAPPRDPAVLSVLAGWRALPAWARGEAPALRADALCHGDLHLGQLVRHPAPDGPWLLIDMDDAGVGDPAWDLGRPAAWYAAGLLAPEDWSTFLDAYRAAGGPAVPADGDPWPALDVPARALTVQTAAVALAKCAAEQRDPDDHEQLMIESCARIATLPPELATGPAS
>NZ_CP010833.1|WP_075267274.1|6779891_6780188_+|zf-TFIIB-domain-containing-protein
MMQCPKCHAQMNTYNRNGVQIEQCNGCRGIFLDYGELESLTRLESQWAQQAPPAPPAPQQPYPPAPPAAHAPAWGAPQHGGHYGHRRQKGFGRMLFSS
>NZ_CP010833.1|WP_075268632.1|6780950_6781988_+|chloride-transporter
MARFDGLIASGLQDVTHDPAALDSSGFWVVSADFEGRIVCARFSDVRREAVPAPVPGAWRGPAAGDWTSSLDRDAYTAGVRRIREHIAAGDVYQANLCRVLSAPLPDGGAGADVDALTSLLARGNPAPYAGTIRLPGHGVEIATASPELFLRRDGRTVESGPIKGTGRTEGDLLEKDHAENVMIVDLVRNDLGRVCATGSVSVPDLCVVEKHPGLVHLVSTVRGRLADGAGWPELFAAAFPPGSVTGAPKSSALRIIAELERGPRGPYCGAIGWVDADRGTASLAVGIRTFWIDRTGPAPLLRFGTGAGITWGSDPEREWDETELKASRLLAVASGTHLETGGDA
>NZ_CP010833.1|WP_075267275.1|6781987_6782809_+|aminodeoxychorismate-lyase
MRIWVNGGLRDAGDARLSVLDHGLTVGDGIFETVRTSEGRPFALTRHLDRLTRSARGLGLPDPDHDEVRRAVAAVIDANPVALGRLRITYTGGLSPLGSDRGDHGTSLVVALDGVSRRPDSTAVITVPWTRNERGALAGLKTTSYAENVVALARARERGASEALFPNTADRLCEGTGSNVFVVLGGRIHTPPVASGCLAGITRALAVEWTGAEETDLPMDVLAEADEVFLTSTLRDVQAVHRVDDRELTPEIGPVTAKAMRIFAERADDDLDP
>NZ_CP010833.1|WP_075267276.1|6782849_6783689_+|GNAT-family-N-acetyltransferase
MTTTLRPSGPLQEGADGARARHYDVCDNGRPVGSVAISTDDAFGPTAGVLRSLSVEESRRRRGRGVIAALAAEEVLRGWGCTRVRVEVPADNDPARRLAAALGYTERSRNMVKDLGPDTAPLPAGLTSRDMSEEEFAAWRQDAVRAYAQNWIDRGVEPEQARLKSETDHAAHLPDGLATEGMRFRVLLQAGEVVGHVWVALRELEPGAGMAGYVFDVEVREEHRGRGHGRALMLLSEDITRAWHADRLGLHVFASNTPALRLYESLGYTTTRYNLAKAL
>NZ_CP010833.1|WP_075267277.1|6783742_6784261_-|DsbA-family-protein
MSDSTPAAPVVLDLWCDLECPDCHRALDDVRALRARYGDRVEIRLRHFPLEKHKHAFAAAQAAEEAVEQGRGWPYIEALLSRTDDLGRAGEPVLLDVARELGLDTEEFDTALIDGRHLLIVDADHAEGKAIGVTGTPTYVIGDERLDGGKSQEGLRERIEEIVDRTLASQDH

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP010833_20	20.1|5739059|20|NZ_CP010833|PILER-CR	5739059-5739078	20	NZ_CP010833.1	351624-351643	1	0.95
NZ_CP010833_21	21.1|5984672|41|NZ_CP010833|CRISPRCasFinder	5984672-5984712	41	NZ_CP010833.1	5984717-5984757	1	0.976
NZ_CP010833_12	12.2|4115481|19|NZ_CP010833|CRT	4115481-4115499	19	NZ_CP010833.1	1038959-1038977	2	0.895
NZ_CP010833_12	12.2|4115481|19|NZ_CP010833|CRT	4115481-4115499	19	NZ_CP010833.1	2072012-2072030	2	0.895
NZ_CP010833_12	12.2|4115481|19|NZ_CP010833|CRT	4115481-4115499	19	NZ_CP010833.1	4653979-4653997	2	0.895
NZ_CP010833_12	12.2|4115481|19|NZ_CP010833|CRT	4115481-4115499	19	NZ_CP010833.1	4870442-4870460	2	0.895
NZ_CP010833_12	12.4|4115559|19|NZ_CP010833|CRT	4115559-4115577	19	NZ_CP010833.1	1038959-1038977	2	0.895
NZ_CP010833_12	12.4|4115559|19|NZ_CP010833|CRT	4115559-4115577	19	NZ_CP010833.1	2072012-2072030	2	0.895
NZ_CP010833_12	12.4|4115559|19|NZ_CP010833|CRT	4115559-4115577	19	NZ_CP010833.1	4653979-4653997	2	0.895
NZ_CP010833_12	12.4|4115559|19|NZ_CP010833|CRT	4115559-4115577	19	NZ_CP010833.1	4870442-4870460	2	0.895
NZ_CP010833_12	12.6|4115637|19|NZ_CP010833|CRT	4115637-4115655	19	NZ_CP010833.1	1038959-1038977	2	0.895
NZ_CP010833_12	12.6|4115637|19|NZ_CP010833|CRT	4115637-4115655	19	NZ_CP010833.1	2072012-2072030	2	0.895
NZ_CP010833_12	12.6|4115637|19|NZ_CP010833|CRT	4115637-4115655	19	NZ_CP010833.1	4653979-4653997	2	0.895
NZ_CP010833_12	12.6|4115637|19|NZ_CP010833|CRT	4115637-4115655	19	NZ_CP010833.1	4870442-4870460	2	0.895
NZ_CP010833_12	12.8|4115715|19|NZ_CP010833|CRT	4115715-4115733	19	NZ_CP010833.1	7695385-7695403	2	0.895
NZ_CP010833_12	12.8|4115715|19|NZ_CP010833|CRT	4115715-4115733	19	NZ_CP010833.1	1038959-1038977	2	0.895
NZ_CP010833_12	12.10|4115793|19|NZ_CP010833|CRT	4115793-4115811	19	NZ_CP010833.1	2072012-2072030	2	0.895
NZ_CP010833_18	18.1|5046848|19|NZ_CP010833|CRT	5046848-5046866	19	NZ_CP010833.1	4229750-4229768	2	0.895
NZ_CP010833_18	18.1|5046848|19|NZ_CP010833|CRT	5046848-5046866	19	NZ_CP010833.1	5708968-5708986	2	0.895
NZ_CP010833_18	18.1|5046848|19|NZ_CP010833|CRT	5046848-5046866	19	NZ_CP010833.1	6404124-6404142	2	0.895
NZ_CP010833_18	18.1|5046848|19|NZ_CP010833|CRT	5046848-5046866	19	NZ_CP010833.1	7418755-7418773	2	0.895
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	NZ_CP010833.1	5435574-5435605	2	0.938

1. spacer 20.1|5739059|20|NZ_CP010833|PILER-CR matches to position: 351624-351643, mismatch: 1, identity: 0.95

gcccgcgccaaggcccggag	CRISPR spacer
gcccgcgccaaggcgcggag	Protospacer
************** *****

2. spacer 21.1|5984672|41|NZ_CP010833|CRISPRCasFinder matches to position: 5984717-5984757, mismatch: 1, identity: 0.976

gtacagccggggccccggccgcacgcagtcggtggaccggc	CRISPR spacer
gtacagccggagccccggccgcacgcagtcggtggaccggc	Protospacer
**********.******************************

3. spacer 12.2|4115481|19|NZ_CP010833|CRT matches to position: 1038959-1038977, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggcggcggggatgacctt	Protospacer
********* ****** **

4. spacer 12.2|4115481|19|NZ_CP010833|CRT matches to position: 2072012-2072030, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggaagcggcgatgacgtt	Protospacer
*** .**************

5. spacer 12.2|4115481|19|NZ_CP010833|CRT matches to position: 4653979-4653997, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
agacggcggcgatggcgtt	Protospacer
**.***********.****

6. spacer 12.2|4115481|19|NZ_CP010833|CRT matches to position: 4870442-4870460, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggcggccgcgatggcgtt	Protospacer
******* ******.****

7. spacer 12.4|4115559|19|NZ_CP010833|CRT matches to position: 1038959-1038977, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggcggcggggatgacctt	Protospacer
********* ****** **

8. spacer 12.4|4115559|19|NZ_CP010833|CRT matches to position: 2072012-2072030, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggaagcggcgatgacgtt	Protospacer
*** .**************

9. spacer 12.4|4115559|19|NZ_CP010833|CRT matches to position: 4653979-4653997, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
agacggcggcgatggcgtt	Protospacer
**.***********.****

10. spacer 12.4|4115559|19|NZ_CP010833|CRT matches to position: 4870442-4870460, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggcggccgcgatggcgtt	Protospacer
******* ******.****

11. spacer 12.6|4115637|19|NZ_CP010833|CRT matches to position: 1038959-1038977, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggcggcggggatgacctt	Protospacer
********* ****** **

12. spacer 12.6|4115637|19|NZ_CP010833|CRT matches to position: 2072012-2072030, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggaagcggcgatgacgtt	Protospacer
*** .**************

13. spacer 12.6|4115637|19|NZ_CP010833|CRT matches to position: 4653979-4653997, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
agacggcggcgatggcgtt	Protospacer
**.***********.****

14. spacer 12.6|4115637|19|NZ_CP010833|CRT matches to position: 4870442-4870460, mismatch: 2, identity: 0.895

aggcggcggcgatgacgtt	CRISPR spacer
aggcggccgcgatggcgtt	Protospacer
******* ******.****

15. spacer 12.8|4115715|19|NZ_CP010833|CRT matches to position: 7695385-7695403, mismatch: 2, identity: 0.895

aggcggcggtgatgacgtt	CRISPR spacer
aggccgcgttgatgacgtt	Protospacer
**** *** **********

16. spacer 12.8|4115715|19|NZ_CP010833|CRT matches to position: 1038959-1038977, mismatch: 2, identity: 0.895

aggcggcggtgatgacgtt	CRISPR spacer
aggcggcggggatgacctt	Protospacer
********* ****** **

17. spacer 12.10|4115793|19|NZ_CP010833|CRT matches to position: 2072012-2072030, mismatch: 2, identity: 0.895

agggggcggcgatgacgtt	CRISPR spacer
aggaagcggcgatgacgtt	Protospacer
***..**************

18. spacer 18.1|5046848|19|NZ_CP010833|CRT matches to position: 4229750-4229768, mismatch: 2, identity: 0.895

gaccggcgagaccaccacc	CRISPR spacer
gacccgcgagtccaccacc	Protospacer
**** ***** ********

19. spacer 18.1|5046848|19|NZ_CP010833|CRT matches to position: 5708968-5708986, mismatch: 2, identity: 0.895

gaccggcgagaccaccacc	CRISPR spacer
gaccagcgagaacaccacc	Protospacer
****.****** *******

20. spacer 18.1|5046848|19|NZ_CP010833|CRT matches to position: 6404124-6404142, mismatch: 2, identity: 0.895

gaccggcgagaccaccacc	CRISPR spacer
gaccggcgagaacagcacc	Protospacer
*********** ** ****

21. spacer 18.1|5046848|19|NZ_CP010833|CRT matches to position: 7418755-7418773, mismatch: 2, identity: 0.895

gaccggcgagaccaccacc	CRISPR spacer
gaccgccgagaccaccccc	Protospacer
***** ********** **

22. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to position: 5435574-5435605, mismatch: 2, identity: 0.938

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tccgtgatcgggcacctggagtggcagccggg	Protospacer
** ******** ********************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	CP054922	Streptomyces sp. NA03103 plasmid unnamed2, complete sequence	17556-17588	0	1.0
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	CP054922	Streptomyces sp. NA03103 plasmid unnamed2, complete sequence	17557-17588	0	1.0
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MH744418	Streptomyces phage JustBecause, complete genome	77090-77122	1	0.97
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MT310898	Streptomyces phage Kela, complete genome	76970-77002	1	0.97
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MH744420	Streptomyces phage Kromp, complete genome	22774-22805	1	0.969
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MH744418	Streptomyces phage JustBecause, complete genome	77091-77122	1	0.969
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MT310898	Streptomyces phage Kela, complete genome	76971-77002	1	0.969
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MH744420	Streptomyces phage Kromp, complete genome	22773-22805	2	0.939
NZ_CP010833_20	20.33|5740883|33|NZ_CP010833|CRISPRCasFinder	5740883-5740915	33	NC_015951	Streptomyces violaceusniger Tu 4113 plasmid pSTRVI01, complete sequence	249526-249558	2	0.939
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MT711977	Streptomyces phage Dagobah, complete genome	23326-23357	2	0.938
NZ_CP010833_20	20.66|5740884|32|NZ_CP010833|CRT	5740884-5740915	32	NC_015951	Streptomyces violaceusniger Tu 4113 plasmid pSTRVI01, complete sequence	249527-249558	2	0.938
NZ_CP010833_3	3.1|158031|25|NZ_CP010833|CRISPRCasFinder	158031-158055	25	NZ_CP009292	Novosphingobium pentaromativorans US6-1 plasmid pLA3, complete sequence	606677-606701	3	0.88
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MT711977	Streptomyces phage Dagobah, complete genome	23326-23358	3	0.909
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MH576962	Streptomyces phage Satis, complete genome	78017-78048	4	0.875
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MK620894	Streptomyces phage Kradal, complete genome	78021-78052	4	0.875
NZ_CP010833_9	9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636708-3636740	33	NZ_CP015737	Shinella sp. HZN7 plasmid pShin-01, complete sequence	7591-7623	5	0.848
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP029209	Nitratireductor sp. OM-1 plasmid pOM-1, complete sequence	729038-729071	5	0.853
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MH576962	Streptomyces phage Satis, complete genome	78016-78048	5	0.848
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MK620894	Streptomyces phage Kradal, complete genome	78020-78052	5	0.848
NZ_CP010833_20	20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740331-5740363	33	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	107614-107646	5	0.848
NZ_CP010833_20	20.51|5739965|32|NZ_CP010833|CRT	5739965-5739996	32	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	2408972-2409003	5	0.844
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	CP006880	Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence	2413336-2413367	5	0.844
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	NZ_CP038031	Rhodococcus ruber strain R1 plasmid unnamed1, complete sequence	8058-8089	5	0.844
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NC_004808	Streptomyces rochei plasmid pSLA2-L DNA, complete sequence	107615-107646	5	0.844
NZ_CP010833_1	1.1|27001|34|NZ_CP010833|CRISPRCasFinder	27001-27034	34	MK411746	Arthrobacter phage Sonali, complete genome	9797-9830	6	0.824
NZ_CP010833_7	7.1|2052446|30|NZ_CP010833|CRISPRCasFinder	2052446-2052475	30	NC_016626	Burkholderia sp. YI23 plasmid byi_1p, complete sequence	861255-861284	6	0.8
NZ_CP010833_8	8.1|3350090|30|NZ_CP010833|CRISPRCasFinder	3350090-3350119	30	MH617052	Microviridae sp. isolate ctdc172, complete genome	3833-3862	6	0.8
NZ_CP010833_20	20.18|5739964|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739964-5739996	33	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	2408972-2409004	6	0.818
NZ_CP010833_20	20.19|5740025|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740025-5740057	33	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	181344-181376	6	0.818
NZ_CP010833_20	20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740331-5740363	33	NZ_CP026519	Deinococcus sp. NW-56 plasmid unnamed3, complete sequence	39097-39129	6	0.818
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_LR594660	Variovorax sp. PBL-H6 plasmid 2	31360-31392	6	0.818
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_LR594667	Variovorax sp. SRS16 plasmid 2	769010-769042	6	0.818
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_LR594690	Variovorax sp. WDL1 plasmid 2	784775-784807	6	0.818
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_LR594672	Variovorax sp. PBL-E5 plasmid 2	769144-769176	6	0.818
NZ_CP010833_20	20.42|5739416|32|NZ_CP010833|CRT	5739416-5739447	32	NZ_CP022317	Brachybacterium avium strain VR2415 plasmid unnamed1	26120-26151	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	LN907801	unidentified phage genome assembly 2P1, chromosome : 2P1	20281-20312	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	AY394005	Bacteriophage D3112, complete genome	20917-20948	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	JN811560	Pseudomonas phage JBD26, complete genome	21035-21066	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MH643777	Pseudomonas phage YMC12/01/R960, complete genome	19934-19965	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511031	Pseudomonas phage BR52, partial genome	14090-14121	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511034	Pseudomonas phage BR243, partial genome	20730-20761	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511033	Pseudomonas phage BR205, partial genome	20795-20826	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NC_027298	Pseudomonas phage LPB1, complate genome	20008-20039	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511017	Pseudomonas phage CF23, partial genome	20746-20777	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	KM389264	UNVERIFIED: Pseudomonas phage F_ET2439sp/Pa1651 clone ctg7180000000634 genomic sequence	2738-2769	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	KM389326	UNVERIFIED: Pseudomonas phage F_KK2074sp/Pa1651 clone contig00001 genomic sequence	18020-18051	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK144667	Pseudomonas phage Spike, complete genome	20792-20823	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MH643778	Pseudomonas phage YMC12/01/R24, complete genome	20394-20425	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	KM389462	UNVERIFIED: Pseudomonas phage JBD23 clone contig00001 genomic sequence	16780-16811	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	JQ067085	Pseudomonas phage PaMx73, complete genome	19770-19801	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	KT968832	Pseudomonas phage YMC11/11/R1836, complete genome	20493-20524	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511026	Pseudomonas phage CF121, partial genome	20698-20729	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NC_005178	Pseudomonas phage D3112, complete genome	20917-20948	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	KM389464	UNVERIFIED: Pseudomonas phage JBDs5 clone contig00001 genomic sequence	16788-16819	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NC_023700	Pseudomonas phage PA1/KOR/2010, complete genome	17744-17775	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511022	Pseudomonas phage CF74, partial genome	23359-23390	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	KM389336	UNVERIFIED: Pseudomonas phage JBD58a clone contig00001 genomic sequence	1678-1709	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511030	Pseudomonas phage CF213, partial genome	20696-20727	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511025	Pseudomonas phage CF118, partial genome	20725-20756	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511023	Pseudomonas phage CF77, partial genome	20696-20727	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	MK511029	Pseudomonas phage CF183, partial genome	21480-21511	6	0.812
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	EU272036	Pseudomonas phage MP29, complete genome	19827-19858	6	0.812
NZ_CP010833_20	20.46|5739660|32|NZ_CP010833|CRT	5739660-5739691	32	MN234199	Mycobacterium phage Ekdilam, complete genome	42908-42939	6	0.812
NZ_CP010833_20	20.47|5739721|32|NZ_CP010833|CRT	5739721-5739752	32	NZ_CP010858	Marinovum algicola DG 898 plasmid pMaD3	160029-160060	6	0.812
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NC_018532	Arthrobacter sp. Rue61a plasmid p232, complete sequence	30162-30193	6	0.812
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	181345-181376	6	0.812
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	MK524500	Mycobacterium phage Kevin1, complete genome	41750-41781	6	0.812
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_CP026519	Deinococcus sp. NW-56 plasmid unnamed3, complete sequence	39097-39128	6	0.812
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	648551-648582	6	0.812
NZ_CP010833_20	20.65|5740825|30|NZ_CP010833|CRT	5740825-5740854	30	NZ_CP022193	Yangia pacifica strain YSBP01 plasmid unnamed3, complete sequence	147351-147380	6	0.8
NZ_CP010833_20	20.65|5740825|30|NZ_CP010833|CRT	5740825-5740854	30	NZ_CP011248	Agrobacterium tumefaciens strain Ach5 plasmid pAt, complete sequence	194792-194821	6	0.8
NZ_CP010833_20	20.65|5740825|30|NZ_CP010833|CRT	5740825-5740854	30	NZ_CP032919	Agrobacterium tumefaciens strain 15955 plasmid pAt15955, complete sequence	194553-194582	6	0.8
NZ_CP010833_20	20.65|5740825|30|NZ_CP010833|CRT	5740825-5740854	30	NZ_CP033029	Agrobacterium tumefaciens strain A6 plasmid pAtA6, complete sequence	194637-194666	6	0.8
NZ_CP010833_1	1.1|27001|34|NZ_CP010833|CRISPRCasFinder	27001-27034	34	MF668280	Mycobacterium phage Phabba, complete genome	68991-69024	7	0.794
NZ_CP010833_7	7.1|2052446|30|NZ_CP010833|CRISPRCasFinder	2052446-2052475	30	NC_019957	Mycobacterium sp. JS623 plasmid pMYCSM01, complete sequence	269601-269630	7	0.767
NZ_CP010833_9	9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636708-3636740	33	NZ_CP038636	Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence	1023331-1023363	7	0.788
NZ_CP010833_9	9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636708-3636740	33	NZ_CP040720	Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence	122861-122893	7	0.788
NZ_CP010833_9	9.3|3636830|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636830-3636862	33	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1196066-1196098	7	0.788
NZ_CP010833_9	9.3|3636830|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636830-3636862	33	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	960753-960785	7	0.788
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP049244	Rhizobium pseudoryzae strain DSM 19479 plasmid unnamed3, complete sequence	576377-576410	7	0.794
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_LR134451	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence	48739-48772	7	0.794
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP054036	Rhizobium sp. JKLM13E plasmid pPR13E05, complete sequence	130931-130964	7	0.794
NZ_CP010833_14	14.1|4706425|35|NZ_CP010833|CRISPRCasFinder	4706425-4706459	35	EU982300	Pseudomonas phage DVM-2008, genomic sequence	7772-7806	7	0.8
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP012701	Sphingopyxis macrogoltabida strain EY-1 isolate activated sludge plasmid 1, complete sequence	16993-17025	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	297738-297770	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	KM389264	UNVERIFIED: Pseudomonas phage F_ET2439sp/Pa1651 clone ctg7180000000634 genomic sequence	2738-2770	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	KM389326	UNVERIFIED: Pseudomonas phage F_KK2074sp/Pa1651 clone contig00001 genomic sequence	18020-18052	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	KM389462	UNVERIFIED: Pseudomonas phage JBD23 clone contig00001 genomic sequence	16780-16812	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	KM389464	UNVERIFIED: Pseudomonas phage JBDs5 clone contig00001 genomic sequence	16788-16820	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	LN907801	unidentified phage genome assembly 2P1, chromosome : 2P1	20280-20312	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	AY394005	Bacteriophage D3112, complete genome	20916-20948	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	JN811560	Pseudomonas phage JBD26, complete genome	21034-21066	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MH643777	Pseudomonas phage YMC12/01/R960, complete genome	19933-19965	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511031	Pseudomonas phage BR52, partial genome	14089-14121	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511034	Pseudomonas phage BR243, partial genome	20729-20761	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511033	Pseudomonas phage BR205, partial genome	20794-20826	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	NC_027298	Pseudomonas phage LPB1, complate genome	20007-20039	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511017	Pseudomonas phage CF23, partial genome	20745-20777	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK144667	Pseudomonas phage Spike, complete genome	20791-20823	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MH643778	Pseudomonas phage YMC12/01/R24, complete genome	20393-20425	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	JQ067085	Pseudomonas phage PaMx73, complete genome	19769-19801	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	KT968832	Pseudomonas phage YMC11/11/R1836, complete genome	20492-20524	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511026	Pseudomonas phage CF121, partial genome	20697-20729	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	NC_005178	Pseudomonas phage D3112, complete genome	20916-20948	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	NC_023700	Pseudomonas phage PA1/KOR/2010, complete genome	17743-17775	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511022	Pseudomonas phage CF74, partial genome	23358-23390	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	KM389336	UNVERIFIED: Pseudomonas phage JBD58a clone contig00001 genomic sequence	1677-1709	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511030	Pseudomonas phage CF213, partial genome	20695-20727	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511025	Pseudomonas phage CF118, partial genome	20724-20756	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511023	Pseudomonas phage CF77, partial genome	20695-20727	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	MK511029	Pseudomonas phage CF183, partial genome	21479-21511	7	0.788
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	EU272036	Pseudomonas phage MP29, complete genome	19826-19858	7	0.788
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MT451982	Streptomyces phage Cumberbatch, complete genome	17504-17536	7	0.788
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MT451980	Streptomyces phage Ignacio, complete genome	17519-17551	7	0.788
NZ_CP010833_20	20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740331-5740363	33	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	648551-648583	7	0.788
NZ_CP010833_20	20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740331-5740363	33	NZ_CP045374	Sulfitobacter sp. THAF37 plasmid pTHAF37_b, complete sequence	29310-29342	7	0.788
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	CP027480	Pseudomonas koreensis strain P19E3 plasmid p3, complete sequence	54122-54154	7	0.788
NZ_CP010833_20	20.31|5740763|33|NZ_CP010833|CRISPRCasFinder	5740763-5740795	33	NZ_CP018064	Rhodococcus sp. 2G plasmid p1, complete sequence	268640-268672	7	0.788
NZ_CP010833_20	20.32|5740824|31|NZ_CP010833|CRISPRCasFinder	5740824-5740854	31	NZ_CP022193	Yangia pacifica strain YSBP01 plasmid unnamed3, complete sequence	147350-147380	7	0.774
NZ_CP010833_20	20.32|5740824|31|NZ_CP010833|CRISPRCasFinder	5740824-5740854	31	NZ_CP020811	Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed2, complete sequence	145266-145296	7	0.774
NZ_CP010833_20	20.32|5740824|31|NZ_CP010833|CRISPRCasFinder	5740824-5740854	31	NZ_CP011248	Agrobacterium tumefaciens strain Ach5 plasmid pAt, complete sequence	194792-194822	7	0.774
NZ_CP010833_20	20.32|5740824|31|NZ_CP010833|CRISPRCasFinder	5740824-5740854	31	NZ_CP032919	Agrobacterium tumefaciens strain 15955 plasmid pAt15955, complete sequence	194553-194583	7	0.774
NZ_CP010833_20	20.32|5740824|31|NZ_CP010833|CRISPRCasFinder	5740824-5740854	31	NZ_CP033029	Agrobacterium tumefaciens strain A6 plasmid pAtA6, complete sequence	194637-194667	7	0.774
NZ_CP010833_20	20.34|5740944|32|NZ_CP010833|CRISPRCasFinder	5740944-5740975	32	NZ_CP031166	Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence	270398-270429	7	0.781
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP012701	Sphingopyxis macrogoltabida strain EY-1 isolate activated sludge plasmid 1, complete sequence	16994-17025	7	0.781
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	73405-73436	7	0.781
NZ_CP010833_20	20.42|5739416|32|NZ_CP010833|CRT	5739416-5739447	32	NZ_CP017947	Bosea sp. Tri-49 plasmid unnamed1, complete sequence	45452-45483	7	0.781
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	297739-297770	7	0.781
NZ_CP010833_20	20.47|5739721|32|NZ_CP010833|CRT	5739721-5739752	32	NZ_AP018829	Asticcacaulis excentricus strain M6 plasmid pASEM-1, complete sequence	34460-34491	7	0.781
NZ_CP010833_20	20.50|5739904|32|NZ_CP010833|CRT	5739904-5739935	32	NZ_CP013109	Sinorhizobium americanum strain CFNEI 73 plasmid B, complete sequence	324066-324097	7	0.781
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NZ_CP017422	Arthrobacter sp. ZXY-2 plasmid pZXY21, complete sequence	266029-266060	7	0.781
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MT451982	Streptomyces phage Cumberbatch, complete genome	17505-17536	7	0.781
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MT451980	Streptomyces phage Ignacio, complete genome	17520-17551	7	0.781
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	182478-182509	7	0.781
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	511359-511390	7	0.781
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NC_008269	Rhodococcus jostii RHA1 plasmid pRHL1, complete sequence	1018269-1018300	7	0.781
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	13732-13763	7	0.781
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	724687-724718	7	0.781
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_CP045374	Sulfitobacter sp. THAF37 plasmid pTHAF37_b, complete sequence	29310-29341	7	0.781
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_CP037916	Sphingomonas sp. AAP5 plasmid p32, complete sequence	25823-25854	7	0.781
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NC_019408	Caulobacter phage CcrRogue, complete genome	38292-38323	7	0.781
NZ_CP010833_20	20.61|5740581|32|NZ_CP010833|CRT	5740581-5740612	32	MT657333	Microbacterium phage Casend, complete genome	814-845	7	0.781
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP016619	Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence	208175-208206	7	0.781
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	MN428048	Gordonia phage DobbysSock, complete genome	433-464	7	0.781
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	CP027480	Pseudomonas koreensis strain P19E3 plasmid p3, complete sequence	54122-54153	7	0.781
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP015867	Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence	159369-159400	7	0.781
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP030263	Ensifer adhaerens strain Corn53 plasmid AA, complete sequence	96875-96906	7	0.781
NZ_CP010833_20	20.64|5740764|32|NZ_CP010833|CRT	5740764-5740795	32	NZ_CP018064	Rhodococcus sp. 2G plasmid p1, complete sequence	268640-268671	7	0.781
NZ_CP010833_20	20.65|5740825|30|NZ_CP010833|CRT	5740825-5740854	30	NZ_CP020811	Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed2, complete sequence	145267-145296	7	0.767
NZ_CP010833_20	20.66|5740884|32|NZ_CP010833|CRT	5740884-5740915	32	CP054927	Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence	485956-485987	7	0.781
NZ_CP010833_20	20.67|5740945|31|NZ_CP010833|CRT	5740945-5740975	31	NZ_CP031166	Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence	270398-270428	7	0.774
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1355730-1355758	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022775	Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence	464257-464285	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NC_014310	Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence	442028-442056	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022762	Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence	430837-430865	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	457341-457369	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP023017	Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence	419159-419187	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP014703	Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence	430837-430865	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022760	Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence	426272-426300	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022789	Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence	426262-426290	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022771	Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence	430849-430877	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022777	Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence	430870-430898	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022799	Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence	430836-430864	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022764	Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence	464291-464319	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022797	Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence	464291-464319	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	NZ_CP022758	Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence	464282-464310	7	0.759
NZ_CP010833_23	23.1|6773828|29|NZ_CP010833|CRISPRCasFinder	6773828-6773856	29	MH744418	Streptomyces phage JustBecause, complete genome	158781-158809	7	0.759
NZ_CP010833_9	9.2|3636769|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636769-3636801	33	NZ_CP029777	Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence	130033-130065	8	0.758
NZ_CP010833_20	20.3|5739049|33|NZ_CP010833|CRISPRCasFinder	5739049-5739081	33	LN997845	Streptomyces reticuli genome assembly TUE45, plasmid : IV	53372-53404	8	0.758
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NC_014007	Sphingobium japonicum UT26S plasmid pCHQ1, complete sequence	171291-171323	8	0.758
NZ_CP010833_20	20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740209-5740241	33	MT451981	Streptomyces phage Vondra, complete genome	17518-17550	8	0.758
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	182478-182510	8	0.758
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	511358-511390	8	0.758
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	13731-13763	8	0.758
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	724686-724718	8	0.758
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	MK310144	Mycobacterium phage CicholasNage, complete genome	61768-61800	8	0.758
NZ_CP010833_20	20.28|5740580|33|NZ_CP010833|CRISPRCasFinder	5740580-5740612	33	MT657333	Microbacterium phage Casend, complete genome	814-846	8	0.758
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_CP016619	Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence	208174-208206	8	0.758
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	MN428048	Gordonia phage DobbysSock, complete genome	433-465	8	0.758
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_KX443388	Rhodococcus hoagii strain PAM1216 plasmid pVAPA1216, complete sequence	16635-16667	8	0.758
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_CP013256	Kocuria flava strain HO-9041 plasmid 2, complete sequence	8868-8900	8	0.758
NZ_CP010833_20	20.32|5740824|31|NZ_CP010833|CRISPRCasFinder	5740824-5740854	31	NZ_CP021082	Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence	609426-609456	8	0.742
NZ_CP010833_20	20.34|5740944|32|NZ_CP010833|CRISPRCasFinder	5740944-5740975	32	NZ_CP019585	Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymA, complete sequence	32025-32056	8	0.75
NZ_CP010833_20	20.34|5740944|32|NZ_CP010833|CRISPRCasFinder	5740944-5740975	32	NC_017324	Sinorhizobium meliloti BL225C plasmid pSINMEB01, complete sequence	352237-352268	8	0.75
NZ_CP010833_20	20.34|5740944|32|NZ_CP010833|CRISPRCasFinder	5740944-5740975	32	NZ_CP021827	Sinorhizobium meliloti strain KH35c plasmid psymA, complete sequence	152870-152901	8	0.75
NZ_CP010833_20	20.36|5739050|32|NZ_CP010833|CRT	5739050-5739081	32	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	636936-636967	8	0.75
NZ_CP010833_20	20.36|5739050|32|NZ_CP010833|CRT	5739050-5739081	32	LN997845	Streptomyces reticuli genome assembly TUE45, plasmid : IV	53372-53403	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP013597	Rhizobium sp. N741 plasmid pRspN741b, complete sequence	274548-274579	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP013501	Rhizobium esperanzae strain N561 plasmid pRspN561a, complete sequence	274914-274945	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP013507	Rhizobium sp. N1341 plasmid pRspN1341b, complete sequence	274548-274579	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP013518	Rhizobium sp. N113 plasmid pRspN113a, complete sequence	274914-274945	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP013491	Rhizobium sp. N6212 plasmid pRspN6212a, complete sequence	274917-274948	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP013496	Rhizobium sp. N621 plasmid pRspN621a, complete sequence	274917-274948	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP013591	Rhizobium sp. N871 plasmid pRspN871a, complete sequence	274917-274948	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NC_014007	Sphingobium japonicum UT26S plasmid pCHQ1, complete sequence	171292-171323	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP050082	Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b4, complete sequence	286302-286333	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NC_008384	Rhizobium leguminosarum bv. viciae 3841 plasmid pRL11, complete sequence	245699-245730	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP049732	Rhizobium leguminosarum strain A1 plasmid pRL11, complete sequence	234578-234609	8	0.75
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_LR134465	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence	378335-378366	8	0.75
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	341608-341639	8	0.75
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	GQ919031	Streptomyces phage ZL12, complete genome	24391-24422	8	0.75
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NZ_CP033583	Streptomyces sp. ADI95-16 plasmid pADI95-16b, complete sequence	187479-187510	8	0.75
NZ_CP010833_20	20.46|5739660|32|NZ_CP010833|CRT	5739660-5739691	32	NZ_CP017077	Novosphingobium resinovorum strain SA1 plasmid pSA2, complete sequence	187373-187404	8	0.75
NZ_CP010833_20	20.50|5739904|32|NZ_CP010833|CRT	5739904-5739935	32	NZ_CP017947	Bosea sp. Tri-49 plasmid unnamed1, complete sequence	260933-260964	8	0.75
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NZ_CP044425	Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence	391097-391128	8	0.75
NZ_CP010833_20	20.53|5740087|33|NZ_CP010833|CRT	5740087-5740119	33	MF417926	Uncultured Caudovirales phage clone 9F_1, partial genome	18653-18685	8	0.758
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	MT451981	Streptomyces phage Vondra, complete genome	17519-17550	8	0.75
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	208801-208832	8	0.75
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	838419-838450	8	0.75
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	MK310144	Mycobacterium phage CicholasNage, complete genome	61768-61799	8	0.75
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	4405947-4405978	8	0.75
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_CP023064	Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence	130681-130712	8	0.75
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_CP047174	Rathayibacter sp. VKM Ac-2760 plasmid unnamed1, complete sequence	87511-87542	8	0.75
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_CP015881	Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence	608454-608485	8	0.75
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_AP022607	Mycobacterium branderi strain JCM 12687 plasmid pJCM12687	841886-841917	8	0.75
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_CP030263	Ensifer adhaerens strain Corn53 plasmid AA, complete sequence	1608627-1608658	8	0.75
NZ_CP010833_20	20.58|5740393|32|NZ_CP010833|CRT	5740393-5740424	32	NZ_LR594692	Variovorax sp. WDL1 plasmid 4	139726-139757	8	0.75
NZ_CP010833_20	20.60|5740520|32|NZ_CP010833|CRT	5740520-5740551	32	NC_011356	Enterobacteria phage YYZ-2008, complete prophage genome	54171-54202	8	0.75
NZ_CP010833_20	20.60|5740520|32|NZ_CP010833|CRT	5740520-5740551	32	FJ184280	Enterobacteria phage YYZ-2008, complete genome	54171-54202	8	0.75
NZ_CP010833_20	20.60|5740520|32|NZ_CP010833|CRT	5740520-5740551	32	AP000400	Enterobacteria phage VT1-Sakai genomic DNA, prophage inserted region in Escherichia coli O157:H7	6790-6821	8	0.75
NZ_CP010833_20	20.62|5740642|32|NZ_CP010833|CRT	5740642-5740673	32	NZ_CP016082	Streptomyces sp. SAT1 plasmid unnamed2, complete sequence	36685-36716	8	0.75
NZ_CP010833_20	20.62|5740642|32|NZ_CP010833|CRT	5740642-5740673	32	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	306533-306564	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_LR594660	Variovorax sp. PBL-H6 plasmid 2	31360-31391	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_LR594667	Variovorax sp. SRS16 plasmid 2	769011-769042	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_LR594690	Variovorax sp. WDL1 plasmid 2	784776-784807	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_LR594672	Variovorax sp. PBL-E5 plasmid 2	769145-769176	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_KX443388	Rhodococcus hoagii strain PAM1216 plasmid pVAPA1216, complete sequence	16636-16667	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP050098	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence	664173-664204	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP013256	Kocuria flava strain HO-9041 plasmid 2, complete sequence	8868-8899	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP053440	Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence	734892-734923	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP006990	Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence	556385-556416	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NC_012848	Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence	220585-220616	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	CP007644	Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803c, complete sequence	539915-539946	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP018230	Rhizobium leguminosarum strain Vaf-108 plasmid unnamed2, complete sequence	371645-371676	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP048282	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248d, complete sequence	32974-33005	8	0.75
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	MH045567	Microbacterium phage Elva, complete genome	20989-21020	8	0.75
NZ_CP010833_20	20.67|5740945|31|NZ_CP010833|CRT	5740945-5740975	31	NZ_CP019585	Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymA, complete sequence	32026-32056	8	0.742
NZ_CP010833_20	20.67|5740945|31|NZ_CP010833|CRT	5740945-5740975	31	NC_017324	Sinorhizobium meliloti BL225C plasmid pSINMEB01, complete sequence	352238-352268	8	0.742
NZ_CP010833_20	20.67|5740945|31|NZ_CP010833|CRT	5740945-5740975	31	NZ_CP021827	Sinorhizobium meliloti strain KH35c plasmid psymA, complete sequence	152870-152900	8	0.742
NZ_CP010833_1	1.1|27001|34|NZ_CP010833|CRISPRCasFinder	27001-27034	34	NC_011273	Mycobacterium phage Myrna, complete genome	70018-70051	9	0.735
NZ_CP010833_1	1.1|27001|34|NZ_CP010833|CRISPRCasFinder	27001-27034	34	NC_019957	Mycobacterium sp. JS623 plasmid pMYCSM01, complete sequence	289847-289880	9	0.735
NZ_CP010833_9	9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636708-3636740	33	NZ_CP041156	Leisingera aquaemixtae strain R2C4 plasmid unnamed1, complete sequence	143746-143778	9	0.727
NZ_CP010833_9	9.2|3636769|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636769-3636801	33	MT114163	Mycobacterium phage Settecandela, complete genome	89264-89296	9	0.727
NZ_CP010833_9	9.2|3636769|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636769-3636801	33	MK937592	Mycobacterium phage Phrappuccino, complete genome	89264-89296	9	0.727
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP039693	Agrobacterium larrymoorei strain CFBP5473 plasmid pAlCFBP5473, complete sequence	117251-117284	9	0.735
NZ_CP010833_18	18.5|5047079|31|NZ_CP010833|CRT	5047079-5047109	31	NC_011366	Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG202, complete sequence	231888-231918	9	0.71
NZ_CP010833_18	18.5|5047079|31|NZ_CP010833|CRT	5047079-5047109	31	NZ_CP035001	Rhizobium acidisoli strain FH23 plasmid pRapFH23c, complete sequence	191000-191030	9	0.71
NZ_CP010833_18	18.5|5047079|31|NZ_CP010833|CRT	5047079-5047109	31	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	693507-693537	9	0.71
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP013597	Rhizobium sp. N741 plasmid pRspN741b, complete sequence	274548-274580	9	0.727
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP013501	Rhizobium esperanzae strain N561 plasmid pRspN561a, complete sequence	274914-274946	9	0.727
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP013507	Rhizobium sp. N1341 plasmid pRspN1341b, complete sequence	274548-274580	9	0.727
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP013518	Rhizobium sp. N113 plasmid pRspN113a, complete sequence	274914-274946	9	0.727
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP013491	Rhizobium sp. N6212 plasmid pRspN6212a, complete sequence	274917-274949	9	0.727
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP013496	Rhizobium sp. N621 plasmid pRspN621a, complete sequence	274917-274949	9	0.727
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP013591	Rhizobium sp. N871 plasmid pRspN871a, complete sequence	274917-274949	9	0.727
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP009216	Corynebacterium ureicelerivorans strain IMMIB RIV-2301 plasmid unnamed, complete sequence	4261-4293	9	0.727
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	GQ919031	Streptomyces phage ZL12, complete genome	24390-24422	9	0.727
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	NZ_CP007144	Hymenobacter swuensis DY53 plasmid pHsw1, complete sequence	289555-289587	9	0.727
NZ_CP010833_20	20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739476-5739508	33	NZ_CP033583	Streptomyces sp. ADI95-16 plasmid pADI95-16b, complete sequence	187479-187511	9	0.727
NZ_CP010833_20	20.17|5739903|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739903-5739935	33	MH001458	Mycobacterium phage Smeagol, complete genome	31507-31539	9	0.727
NZ_CP010833_20	20.19|5740025|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740025-5740057	33	NZ_CP044425	Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence	391097-391129	9	0.727
NZ_CP010833_20	20.20|5740086|34|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740086-5740119	34	MF417926	Uncultured Caudovirales phage clone 9F_1, partial genome	18652-18685	9	0.735
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	838419-838451	9	0.727
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	208800-208832	9	0.727
NZ_CP010833_20	20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740331-5740363	33	NZ_CP023064	Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence	130681-130713	9	0.727
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	MK376956	Gordonia phage WilliamBoone, complete genome	69066-69098	9	0.727
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_CP050098	Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence	664173-664205	9	0.727
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_CP053440	Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence	734892-734924	9	0.727
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_CP006990	Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence	556385-556417	9	0.727
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NC_012848	Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence	220585-220617	9	0.727
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	CP007644	Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803c, complete sequence	539915-539947	9	0.727
NZ_CP010833_20	20.36|5739050|32|NZ_CP010833|CRT	5739050-5739081	32	NZ_CP041044	Paracoccus sp. AK26 plasmid pAK2, complete sequence	23717-23748	9	0.719
NZ_CP010833_20	20.36|5739050|32|NZ_CP010833|CRT	5739050-5739081	32	NZ_CP045549	Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence	91506-91537	9	0.719
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP009216	Corynebacterium ureicelerivorans strain IMMIB RIV-2301 plasmid unnamed, complete sequence	4261-4292	9	0.719
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	CP047137	Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence	114790-114821	9	0.719
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_LR134460	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 18, complete sequence	263593-263624	9	0.719
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP016821	Rhodococcus sp. p52 plasmid pDF01, complete sequence	9244-9275	9	0.719
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP016822	Rhodococcus sp. p52 plasmid pDF03, complete sequence	12161-12192	9	0.719
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP016822	Rhodococcus sp. p52 plasmid pDF03, complete sequence	94690-94721	9	0.719
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	MT657335	Gordonia phage Mariokart, complete genome	24838-24869	9	0.719
NZ_CP010833_20	20.39|5739233|32|NZ_CP010833|CRT	5739233-5739264	32	NZ_CP021355	Rhodococcus sp. S2-17 plasmid pRB98, complete sequence	910230-910261	9	0.719
NZ_CP010833_20	20.42|5739416|32|NZ_CP010833|CRT	5739416-5739447	32	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	490278-490309	9	0.719
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NZ_CP007144	Hymenobacter swuensis DY53 plasmid pHsw1, complete sequence	289555-289586	9	0.719
NZ_CP010833_20	20.43|5739477|32|NZ_CP010833|CRT	5739477-5739508	32	NZ_CP034813	Paracoccus sp. Arc7-R13 plasmid unnamed2, complete sequence	166999-167030	9	0.719
NZ_CP010833_20	20.49|5739843|32|NZ_CP010833|CRT	5739843-5739874	32	NZ_AF135182	Serratia entomophila strain A1MO2 plasmid pADAP, complete sequence	65174-65205	9	0.719
NZ_CP010833_20	20.49|5739843|32|NZ_CP010833|CRT	5739843-5739874	32	NC_002523	Serratia entomophila plasmid pADAP, complete sequence	65174-65205	9	0.719
NZ_CP010833_20	20.50|5739904|32|NZ_CP010833|CRT	5739904-5739935	32	MH001458	Mycobacterium phage Smeagol, complete genome	31508-31539	9	0.719
NZ_CP010833_20	20.50|5739904|32|NZ_CP010833|CRT	5739904-5739935	32	NZ_CP040819	Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence	232554-232585	9	0.719
NZ_CP010833_20	20.50|5739904|32|NZ_CP010833|CRT	5739904-5739935	32	MN062714	Microbacterium Phage DirtyBubble, complete genome	7640-7671	9	0.719
NZ_CP010833_20	20.50|5739904|32|NZ_CP010833|CRT	5739904-5739935	32	MT024860	Microbacterium phage Stromboli, complete genome	7631-7662	9	0.719
NZ_CP010833_20	20.51|5739965|32|NZ_CP010833|CRT	5739965-5739996	32	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	297268-297299	9	0.719
NZ_CP010833_20	20.51|5739965|32|NZ_CP010833|CRT	5739965-5739996	32	MT708545	Rhizobium phage Pasto, complete genome	30318-30349	9	0.719
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NZ_CP012940	Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence	1624288-1624319	9	0.719
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NZ_CP012944	Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence	1495799-1495830	9	0.719
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NC_017575	Ralstonia solanacearum Po82 megaplasmid, complete sequence	377201-377232	9	0.719
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NZ_CP026308	Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence	377188-377219	9	0.719
NZ_CP010833_20	20.52|5740026|32|NZ_CP010833|CRT	5740026-5740057	32	NZ_CP051295	Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence	1607176-1607207	9	0.719
NZ_CP010833_20	20.55|5740210|32|NZ_CP010833|CRT	5740210-5740241	32	NZ_CP040819	Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence	300147-300178	9	0.719
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_LN831788	Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE1, complete sequence	73659-73690	9	0.719
NZ_CP010833_20	20.61|5740581|32|NZ_CP010833|CRT	5740581-5740612	32	NZ_CP020331	Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence	470401-470432	9	0.719
NZ_CP010833_20	20.61|5740581|32|NZ_CP010833|CRT	5740581-5740612	32	NZ_CP046574	Rhodococcus sp. WAY2 plasmid pRWAY02, complete sequence	26751-26782	9	0.719
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	MK376956	Gordonia phage WilliamBoone, complete genome	69067-69098	9	0.719
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP020897	Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5a, complete sequence	101757-101788	9	0.719
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP022191	Yangia pacifica strain YSBP01 plasmid unnamed1, complete sequence	171157-171188	9	0.719
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP029209	Nitratireductor sp. OM-1 plasmid pOM-1, complete sequence	10038-10069	9	0.719
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP054615	Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence	195781-195812	9	0.719
NZ_CP010833_20	20.66|5740884|32|NZ_CP010833|CRT	5740884-5740915	32	NC_014533	Gloeothece verrucosa PCC 7822 plasmid Cy782201, complete sequence	207808-207839	9	0.719
NZ_CP010833_9	9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636708-3636740	33	NC_007766	Rhizobium etli CFN 42 plasmid p42f, complete sequence	594058-594090	10	0.697
NZ_CP010833_18	18.2|5046890|37|NZ_CP010833|CRT	5046890-5046926	37	AF440695	Virus PhiCh1, complete genome	28694-28730	10	0.73
NZ_CP010833_18	18.2|5046890|37|NZ_CP010833|CRT	5046890-5046926	37	NC_004084	Natrialba phage PhiCh1, complete genome	28694-28730	10	0.73
NZ_CP010833_20	20.3|5739049|33|NZ_CP010833|CRISPRCasFinder	5739049-5739081	33	NZ_CP041044	Paracoccus sp. AK26 plasmid pAK2, complete sequence	23717-23749	10	0.697
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	CP047137	Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence	114789-114821	10	0.697
NZ_CP010833_20	20.5|5739171|33|NZ_CP010833|CRISPRCasFinder	5739171-5739203	33	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	536344-536376	10	0.697
NZ_CP010833_20	20.9|5739415|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5739415-5739447	33	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	490278-490310	10	0.697
NZ_CP010833_20	20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR	5740270-5740302	33	NC_008712	Paenarthrobacter aurescens TC1 plasmid pTC1, complete sequence	137189-137221	10	0.697
NZ_CP010833_20	20.30|5740702|33|NZ_CP010833|CRISPRCasFinder	5740702-5740734	33	NZ_CP025549	Mycobacterium paragordonae strain 49061 plasmid unnamed3, complete sequence	12344-12376	10	0.697
NZ_CP010833_20	20.36|5739050|32|NZ_CP010833|CRT	5739050-5739081	32	NZ_CP029362	Streptomyces globisporus strain TFH56 plasmid pTFSG1, complete sequence	43812-43843	10	0.688
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP021653	Ralstonia solanacearum strain RS 488 plasmid unnamed, complete sequence	27320-27351	10	0.688
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP022366	Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence	536344-536375	10	0.688
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP012688	Ralstonia solanacearum strain UY031 plasmid unnamed, complete sequence	27320-27351	10	0.688
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	CP047139	Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence	125703-125734	10	0.688
NZ_CP010833_20	20.46|5739660|32|NZ_CP010833|CRT	5739660-5739691	32	MK967383	Gordonia phage SweatNTears, complete genome	955-986	10	0.688
NZ_CP010833_20	20.49|5739843|32|NZ_CP010833|CRT	5739843-5739874	32	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	343540-343571	10	0.688
NZ_CP010833_20	20.50|5739904|32|NZ_CP010833|CRT	5739904-5739935	32	KF493880	Mycobacterium phage HanShotFirst, complete genome	29644-29675	10	0.688
NZ_CP010833_20	20.51|5739965|32|NZ_CP010833|CRT	5739965-5739996	32	NZ_CP039632	Pseudomonas veronii strain Pvy plasmid unnamed, complete sequence	76864-76895	10	0.688
NZ_CP010833_20	20.51|5739965|32|NZ_CP010833|CRT	5739965-5739996	32	NC_014918	Mesorhizobium ciceri biovar biserrulae WSM1271 plasmid pMESCI01, complete sequence	258361-258392	10	0.688
NZ_CP010833_20	20.56|5740271|32|NZ_CP010833|CRT	5740271-5740302	32	NC_008712	Paenarthrobacter aurescens TC1 plasmid pTC1, complete sequence	137190-137221	10	0.688
NZ_CP010833_20	20.57|5740332|32|NZ_CP010833|CRT	5740332-5740363	32	NZ_LR594673	Variovorax sp. PBL-E5 plasmid 3	193733-193764	10	0.688
NZ_CP010833_20	20.58|5740393|32|NZ_CP010833|CRT	5740393-5740424	32	NZ_CP048421	Sphingomonas insulae strain KCTC 12872 plasmid unnamed3, complete sequence	82457-82488	10	0.688
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP025549	Mycobacterium paragordonae strain 49061 plasmid unnamed3, complete sequence	12344-12375	10	0.688
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NC_012586	Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence	1451022-1451053	10	0.688
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NC_023497	Amycolatopsis keratiniphila plasmid pXL100, complete sequence	30645-30676	10	0.688
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP023068	Ensifer sojae CCBAU 05684 plasmid pSJ05684b, complete sequence	1405742-1405773	10	0.688
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NC_011758	Methylorubrum extorquens CM4 plasmid pCMU01, complete sequence	245549-245580	10	0.688
NZ_CP010833_20	20.63|5740703|32|NZ_CP010833|CRT	5740703-5740734	32	NZ_CP045549	Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence	61799-61830	10	0.688
NZ_CP010833_9	9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder	3636708-3636740	33	NC_021911	Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1f, complete sequence	206818-206850	11	0.667
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP043441	Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence	2124489-2124522	11	0.676
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NZ_CP035092	Paracoccus denitrificans strain ATCC 19367 plasmid unnamed1, complete sequence	548936-548967	11	0.656
NZ_CP010833_20	20.38|5739172|32|NZ_CP010833|CRT	5739172-5739203	32	NC_008688	Paracoccus denitrificans PD1222 plasmid 1, complete sequence	142469-142500	11	0.656
NZ_CP010833_20	20.41|5739355|32|NZ_CP010833|CRT	5739355-5739386	32	NZ_CP016763	Citrobacter freundii strain B38 plasmid pOZ172, complete sequence	3297-3328	11	0.656
NZ_CP010833_20	20.41|5739355|32|NZ_CP010833|CRT	5739355-5739386	32	NZ_KX839208	Klebsiella pneumoniae strain KP1814 plasmid pKP1814-2, complete sequence	101555-101586	11	0.656
NZ_CP010833_20	20.41|5739355|32|NZ_CP010833|CRT	5739355-5739386	32	CP052526	Klebsiella pneumoniae strain B16KP0177 plasmid pB16KP0177-2, complete sequence	8727-8758	11	0.656
NZ_CP010833_20	20.41|5739355|32|NZ_CP010833|CRT	5739355-5739386	32	NZ_CP017991	Enterobacter cloacae complex sp. ECNIH7 plasmid pENT-1ac, complete sequence	37157-37188	11	0.656
NZ_CP010833_20	20.46|5739660|32|NZ_CP010833|CRT	5739660-5739691	32	NC_017643	Escherichia coli UMNK88 plasmid pUMNK88_Hly, complete sequence	15229-15260	11	0.656
NZ_CP010833_20	20.47|5739721|32|NZ_CP010833|CRT	5739721-5739752	32	NZ_LT900339	Gluconobacter oxydans 621H isolate WT-DSMZ plasmid 2	69710-69741	11	0.656
NZ_CP010833_20	20.47|5739721|32|NZ_CP010833|CRT	5739721-5739752	32	NC_006672	Gluconobacter oxydans 621H plasmid pGOX1, complete sequence	69708-69739	11	0.656
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	1063055-1063088	12	0.647
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	820887-820920	12	0.647
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	286561-286594	12	0.647
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	668459-668492	12	0.647
NZ_CP010833_13	13.1|4698750|34|NZ_CP010833|CRISPRCasFinder	4698750-4698783	34	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1069318-1069351	12	0.647

1. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to CP054922 (Streptomyces sp. NA03103 plasmid unnamed2, complete sequence) position: , mismatch: 0, identity: 1.0

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
gtcggtgatcggccacctggagtggcagccggg	Protospacer
*********************************

2. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to CP054922 (Streptomyces sp. NA03103 plasmid unnamed2, complete sequence) position: , mismatch: 0, identity: 1.0

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tcggtgatcggccacctggagtggcagccggg	Protospacer
********************************

3. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MH744418 (Streptomyces phage JustBecause, complete genome) position: , mismatch: 1, identity: 0.97

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
gtcggtcatcggccacctggagtggcagccggg	Protospacer
****** **************************

4. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MT310898 (Streptomyces phage Kela, complete genome) position: , mismatch: 1, identity: 0.97

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
gtcggtcatcggccacctggagtggcagccggg	Protospacer
****** **************************

5. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MH744420 (Streptomyces phage Kromp, complete genome) position: , mismatch: 1, identity: 0.969

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tcggtgatcgggcacctggagtggcagccggg	Protospacer
*********** ********************

6. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MH744418 (Streptomyces phage JustBecause, complete genome) position: , mismatch: 1, identity: 0.969

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tcggtcatcggccacctggagtggcagccggg	Protospacer
***** **************************

7. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MT310898 (Streptomyces phage Kela, complete genome) position: , mismatch: 1, identity: 0.969

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tcggtcatcggccacctggagtggcagccggg	Protospacer
***** **************************

8. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MH744420 (Streptomyces phage Kromp, complete genome) position: , mismatch: 2, identity: 0.939

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
ctcggtgatcgggcacctggagtggcagccggg	Protospacer
 *********** ********************

9. spacer 20.33|5740883|33|NZ_CP010833|CRISPRCasFinder matches to NC_015951 (Streptomyces violaceusniger Tu 4113 plasmid pSTRVI01, complete sequence) position: , mismatch: 2, identity: 0.939

gaggatcgggatcacggcgtgcattcctacgcc	CRISPR spacer
gaggatcgggatcacggcgtgcatgccgacgcc	Protospacer
************************ ** *****

10. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MT711977 (Streptomyces phage Dagobah, complete genome) position: , mismatch: 2, identity: 0.938

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tcggtcatcggccacctggagtggcagcccgg	Protospacer
***** *********************** **

11. spacer 20.66|5740884|32|NZ_CP010833|CRT matches to NC_015951 (Streptomyces violaceusniger Tu 4113 plasmid pSTRVI01, complete sequence) position: , mismatch: 2, identity: 0.938

aggatcgggatcacggcgtgcattcctacgcc	CRISPR spacer
aggatcgggatcacggcgtgcatgccgacgcc	Protospacer
*********************** ** *****

12. spacer 3.1|158031|25|NZ_CP010833|CRISPRCasFinder matches to NZ_CP009292 (Novosphingobium pentaromativorans US6-1 plasmid pLA3, complete sequence) position: , mismatch: 3, identity: 0.88

cgggccgtggtgcgtcacgggccgt	CRISPR spacer
ggggccgcggtgcgtgacgggccgt	Protospacer
 ******.******* *********

13. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MT711977 (Streptomyces phage Dagobah, complete genome) position: , mismatch: 3, identity: 0.909

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
ttcggtcatcggccacctggagtggcagcccgg	Protospacer
 ***** *********************** **

14. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MH576962 (Streptomyces phage Satis, complete genome) position: , mismatch: 4, identity: 0.875

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tccatcatcggccacctggagtggcagcccgg	Protospacer
** .* *********************** **

15. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MK620894 (Streptomyces phage Kradal, complete genome) position: , mismatch: 4, identity: 0.875

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tccatcatcggccacctggagtggcagcccgg	Protospacer
** .* *********************** **

16. spacer 9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NZ_CP015737 (Shinella sp. HZN7 plasmid pShin-01, complete sequence) position: , mismatch: 5, identity: 0.848

cgactccgtcgccgcggccgcag-ccagatcggg	CRISPR spacer
cgcctccgtcgccgcggcggcagccccgatcga-	Protospacer
** *************** **** ** *****. 

17. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP029209 (Nitratireductor sp. OM-1 plasmid pOM-1, complete sequence) position: , mismatch: 5, identity: 0.853

tgcgttc-ttccgccgcccaccgccgccttgatgg	CRISPR spacer
-gcgttcgagccgccgcccaccgccgccacgatgg	Protospacer
 ******   ****************** .*****

18. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MH576962 (Streptomyces phage Satis, complete genome) position: , mismatch: 5, identity: 0.848

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
ctccatcatcggccacctggagtggcagcccgg	Protospacer
 ** .* *********************** **

19. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK620894 (Streptomyces phage Kradal, complete genome) position: , mismatch: 5, identity: 0.848

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
ctccatcatcggccacctggagtggcagcccgg	Protospacer
 ** .* *********************** **

20. spacer 20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 5, identity: 0.848

gtgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
gagcagcgcttccaggtcgatgtcggccgcgtg	Protospacer
* **  ********************* *** *

21. spacer 20.51|5739965|32|NZ_CP010833|CRT matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.844

aggctagacccggccacggtggaggccgcccg	CRISPR spacer
gggctcgacccggccaccgtggaggccgccaa	Protospacer
.**** *********** ************ .

22. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to CP006880 (Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence) position: , mismatch: 5, identity: 0.844

tcggtgatcggccacctggagt-ggcagccggg	CRISPR spacer
ccggtgatcggcctcctggagcgggcggccgg-	Protospacer
.************ *******. ***.***** 

23. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to NZ_CP038031 (Rhodococcus ruber strain R1 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.844

-tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
cgcggtga-cggccacctggagcagcagccgga	Protospacer
  ****** *************..********.

24. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NC_004808 (Streptomyces rochei plasmid pSLA2-L DNA, complete sequence) position: , mismatch: 5, identity: 0.844

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
agcagcgcttccaggtcgatgtcggccgcgtg	Protospacer
 **  ********************* *** *

25. spacer 1.1|27001|34|NZ_CP010833|CRISPRCasFinder matches to MK411746 (Arthrobacter phage Sonali, complete genome) position: , mismatch: 6, identity: 0.824

gtggccacc-cggaggccacggacaccgtgaccgg	CRISPR spacer
-cggcgaccggggaggccaggggcaccgtgaccgg	Protospacer
 .*** ***  ******** **.************

26. spacer 7.1|2052446|30|NZ_CP010833|CRISPRCasFinder matches to NC_016626 (Burkholderia sp. YI23 plasmid byi_1p, complete sequence) position: , mismatch: 6, identity: 0.8

ggcctgcgtcgaagtcgcctaccactggcg	CRISPR spacer
cgcctgcgtcgaagtggcccaccacggtcc	Protospacer
 ************** ***.***** * * 

27. spacer 8.1|3350090|30|NZ_CP010833|CRISPRCasFinder matches to MH617052 (Microviridae sp. isolate ctdc172, complete genome) position: , mismatch: 6, identity: 0.8

agaggtggcgctcacctggt---ccaagtccac	CRISPR spacer
agaggtggcgctgacctggtcagcgaagtt---	Protospacer
************ *******   * ****.   

28. spacer 20.18|5739964|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.818

gaggctagacccggccacggtggaggccgcccg	CRISPR spacer
cgggctcgacccggccaccgtggaggccgccaa	Protospacer
 .**** *********** ************ .

29. spacer 20.19|5740025|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 6, identity: 0.818

-gcccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
cggtcag-gcggccgagcccatcccggcccgcat	Protospacer
 * .*** ************* .********** 

30. spacer 20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP026519 (Deinococcus sp. NW-56 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.818

gtgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
gcgctccgcttccagggcgaggtcggcggcctt	Protospacer
*.************** *** *********   

31. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_LR594660 (Variovorax sp. PBL-H6 plasmid 2) position: , mismatch: 6, identity: 0.818

--gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
tggcctgca--cgagctcggcgtcaccttgggtga	Protospacer
  * .***.  ****************** *****

32. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_LR594667 (Variovorax sp. SRS16 plasmid 2) position: , mismatch: 6, identity: 0.818

--gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
tggcctgca--cgagctcggcgtcaccttgggtga	Protospacer
  * .***.  ****************** *****

33. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_LR594690 (Variovorax sp. WDL1 plasmid 2) position: , mismatch: 6, identity: 0.818

--gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
tggcctgca--cgagctcggcgtcaccttgggtga	Protospacer
  * .***.  ****************** *****

34. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_LR594672 (Variovorax sp. PBL-E5 plasmid 2) position: , mismatch: 6, identity: 0.818

--gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
tggcctgca--cgagctcggcgtcaccttgggtga	Protospacer
  * .***.  ****************** *****

35. spacer 20.42|5739416|32|NZ_CP010833|CRT matches to NZ_CP022317 (Brachybacterium avium strain VR2415 plasmid unnamed1) position: , mismatch: 6, identity: 0.812

agcgaggagaagcgcctcgcggag--caccgagc	CRISPR spacer
ctcgaggacaagcgcctcgccgagctcaccga--	Protospacer
  ****** *********** ***  ******  

36. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to LN907801 (unidentified phage genome assembly 2P1, chromosome : 2P1) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

37. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to AY394005 (Bacteriophage D3112, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

38. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to JN811560 (Pseudomonas phage JBD26, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

39. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MH643777 (Pseudomonas phage YMC12/01/R960, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

40. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511031 (Pseudomonas phage BR52, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

41. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511034 (Pseudomonas phage BR243, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

42. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511033 (Pseudomonas phage BR205, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

43. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NC_027298 (Pseudomonas phage LPB1, complate genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

44. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511017 (Pseudomonas phage CF23, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

45. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to KM389264 (UNVERIFIED: Pseudomonas phage F_ET2439sp/Pa1651 clone ctg7180000000634 genomic sequence) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

46. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to KM389326 (UNVERIFIED: Pseudomonas phage F_KK2074sp/Pa1651 clone contig00001 genomic sequence) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

47. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK144667 (Pseudomonas phage Spike, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

48. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MH643778 (Pseudomonas phage YMC12/01/R24, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

49. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to KM389462 (UNVERIFIED: Pseudomonas phage JBD23 clone contig00001 genomic sequence) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

50. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to JQ067085 (Pseudomonas phage PaMx73, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

51. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to KT968832 (Pseudomonas phage YMC11/11/R1836, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

52. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511026 (Pseudomonas phage CF121, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

53. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NC_005178 (Pseudomonas phage D3112, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

54. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to KM389464 (UNVERIFIED: Pseudomonas phage JBDs5 clone contig00001 genomic sequence) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

55. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NC_023700 (Pseudomonas phage PA1/KOR/2010, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

56. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511022 (Pseudomonas phage CF74, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

57. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to KM389336 (UNVERIFIED: Pseudomonas phage JBD58a clone contig00001 genomic sequence) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

58. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511030 (Pseudomonas phage CF213, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

59. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511025 (Pseudomonas phage CF118, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

60. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511023 (Pseudomonas phage CF77, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

61. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to MK511029 (Pseudomonas phage CF183, partial genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

62. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to EU272036 (Pseudomonas phage MP29, complete genome) position: , mismatch: 6, identity: 0.812

gactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--ctgaccaccgaccgcaacaccccgctccagga	Protospacer
  ***  *.******************.** ** 

63. spacer 20.46|5739660|32|NZ_CP010833|CRT matches to MN234199 (Mycobacterium phage Ekdilam, complete genome) position: , mismatch: 6, identity: 0.812

tgtcgga-gacgcagcccggcagctgctcgatg	CRISPR spacer
-gcaggacgacgcaacccggcaggtgctcgacg	Protospacer
 *. *** ******.******** *******.*

64. spacer 20.47|5739721|32|NZ_CP010833|CRT matches to NZ_CP010858 (Marinovum algicola DG 898 plasmid pMaD3) position: , mismatch: 6, identity: 0.812

ttcacgggt--gacgcgcggcgactgttcttcgg	CRISPR spacer
--gaagggttcgacgcgcggccactgatcttcgg	Protospacer
   * ****  ********** **** *******

65. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NC_018532 (Arthrobacter sp. Rue61a plasmid p232, complete sequence) position: , mismatch: 6, identity: 0.812

cccagcgcggccgagcccagtccggcccgcag-	CRISPR spacer
gcaagcgcggcccagcccagtccgg-cggcggc	Protospacer
 * ********* ************ * **.* 

66. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 6, identity: 0.812

-cccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
ggtcag-gcggccgagcccatcccggcccgcat	Protospacer
  .*** ************* .********** 

67. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to MK524500 (Mycobacterium phage Kevin1, complete genome) position: , mismatch: 6, identity: 0.812

cccagc--gcggccgagcccagtccggcccgcag	CRISPR spacer
--cagccaaccgccgcgcccaggccggcccgcag	Protospacer
  ****  .* **** ****** ***********

68. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_CP026519 (Deinococcus sp. NW-56 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.812

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
cgctccgcttccagggcgaggtcggcggcctt	Protospacer
.************** *** *********   

69. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 6, identity: 0.812

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
aggtcgccttccaggtcgatgtcggggtcgag	Protospacer
 * **  ****************** * ****

70. spacer 20.65|5740825|30|NZ_CP010833|CRT matches to NZ_CP022193 (Yangia pacifica strain YSBP01 plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.8

acgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
gcgaggtgaacatgggcgtcgatgccgccc	Protospacer
.**********.************   **.

71. spacer 20.65|5740825|30|NZ_CP010833|CRT matches to NZ_CP011248 (Agrobacterium tumefaciens strain Ach5 plasmid pAt, complete sequence) position: , mismatch: 6, identity: 0.8

acgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
atgacatgaacgtgagcgtcgatgagaccg	Protospacer
*.** .********.*********** ** 

72. spacer 20.65|5740825|30|NZ_CP010833|CRT matches to NZ_CP032919 (Agrobacterium tumefaciens strain 15955 plasmid pAt15955, complete sequence) position: , mismatch: 6, identity: 0.8

acgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
atgacatgaacgtgagcgtcgatgagaccg	Protospacer
*.** .********.*********** ** 

73. spacer 20.65|5740825|30|NZ_CP010833|CRT matches to NZ_CP033029 (Agrobacterium tumefaciens strain A6 plasmid pAtA6, complete sequence) position: , mismatch: 6, identity: 0.8

acgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
atgacatgaacgtgagcgtcgatgagaccg	Protospacer
*.** .********.*********** ** 

74. spacer 1.1|27001|34|NZ_CP010833|CRISPRCasFinder matches to MF668280 (Mycobacterium phage Phabba, complete genome) position: , mismatch: 7, identity: 0.794

--gtggccacccggaggccacggacaccgtgaccgg	CRISPR spacer
cggtgg--acccggaggacccggacaccgtgacgat	Protospacer
  ****  ********* * ************* . 

75. spacer 7.1|2052446|30|NZ_CP010833|CRISPRCasFinder matches to NC_019957 (Mycobacterium sp. JS623 plasmid pMYCSM01, complete sequence) position: , mismatch: 7, identity: 0.767

ggcctgcgtcgaagtcgcctaccactggcg	CRISPR spacer
ggcctgcgccgacgtcgcctacctggaggg	Protospacer
********.*** **********   .* *

76. spacer 9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NZ_CP038636 (Cupriavidus oxalaticus strain X32 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.788

cgactccgtcgccgcggccgcagccagatcggg	CRISPR spacer
cggctccgtcgccgcggtcgcagccgtggccgg	Protospacer
**.**************.*******. . * **

77. spacer 9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NZ_CP040720 (Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.788

---cgactccgtcgccgcggccgcagccagatcggg	CRISPR spacer
acgcgacc---tcgccgcggccgcagcccgagcggt	Protospacer
   ****.   ***************** ** *** 

78. spacer 9.3|3636830|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 7, identity: 0.788

ggtgttgagggtgtcgagcttcgacactttttg	CRISPR spacer
gctgatgagggtgtccagcttcgacacgtcgag	Protospacer
* ** ********** *********** *.  *

79. spacer 9.3|3636830|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.788

ggtgttgagggtgtcgagcttcgacactttttg	CRISPR spacer
gctgatgagggtgtccagcttcgacacgtcgag	Protospacer
* ** ********** *********** *.  *

80. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP049244 (Rhizobium pseudoryzae strain DSM 19479 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.794

tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
agcggtcttccgccgcccaccgtcgcctccctgt	Protospacer
 *** *****************.*****.  ** 

81. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_LR134451 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence) position: , mismatch: 7, identity: 0.794

-tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
ccgcg-gccaccgccgccgaacgccgccttgatgg	Protospacer
 .***  *. ******** * **************

82. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP054036 (Rhizobium sp. JKLM13E plasmid pPR13E05, complete sequence) position: , mismatch: 7, identity: 0.794

-tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
ccgcg-tccgccgccgcccccggccgccttgatga	Protospacer
 .*** **. ********* * ************.

83. spacer 14.1|4706425|35|NZ_CP010833|CRISPRCasFinder matches to EU982300 (Pseudomonas phage DVM-2008, genomic sequence) position: , mismatch: 7, identity: 0.8

aggggcc--cctccggtgttgtcgtccatcaccactt	CRISPR spacer
--ggaccagcgaccggtgttgtcgtccatgaccgctt	Protospacer
  **.**  *  ***************** ***.***

84. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP012701 (Sphingopyxis macrogoltabida strain EY-1 isolate activated sludge plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.788

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gtcagaccggcgccctcgacgcgccccgctggc	Protospacer
*.* ************** **********. . 

85. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 7, identity: 0.788

ggactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
gaactgcgccgagcgcaccaccccgccggaagc	Protospacer
*.********** **** *********   .**

86. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to KM389264 (UNVERIFIED: Pseudomonas phage F_ET2439sp/Pa1651 clone ctg7180000000634 genomic sequence) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

87. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to KM389326 (UNVERIFIED: Pseudomonas phage F_KK2074sp/Pa1651 clone contig00001 genomic sequence) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

88. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to KM389462 (UNVERIFIED: Pseudomonas phage JBD23 clone contig00001 genomic sequence) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

89. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to KM389464 (UNVERIFIED: Pseudomonas phage JBDs5 clone contig00001 genomic sequence) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

90. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to LN907801 (unidentified phage genome assembly 2P1, chromosome : 2P1) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

91. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to AY394005 (Bacteriophage D3112, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

92. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to JN811560 (Pseudomonas phage JBD26, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

93. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MH643777 (Pseudomonas phage YMC12/01/R960, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

94. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511031 (Pseudomonas phage BR52, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

95. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511034 (Pseudomonas phage BR243, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

96. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511033 (Pseudomonas phage BR205, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

97. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NC_027298 (Pseudomonas phage LPB1, complate genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

98. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511017 (Pseudomonas phage CF23, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

99. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK144667 (Pseudomonas phage Spike, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

100. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MH643778 (Pseudomonas phage YMC12/01/R24, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

101. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to JQ067085 (Pseudomonas phage PaMx73, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

102. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to KT968832 (Pseudomonas phage YMC11/11/R1836, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

103. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511026 (Pseudomonas phage CF121, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

104. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NC_005178 (Pseudomonas phage D3112, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

105. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NC_023700 (Pseudomonas phage PA1/KOR/2010, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

106. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511022 (Pseudomonas phage CF74, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

107. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to KM389336 (UNVERIFIED: Pseudomonas phage JBD58a clone contig00001 genomic sequence) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

108. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511030 (Pseudomonas phage CF213, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

109. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511025 (Pseudomonas phage CF118, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

110. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511023 (Pseudomonas phage CF77, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

111. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK511029 (Pseudomonas phage CF183, partial genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

112. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to EU272036 (Pseudomonas phage MP29, complete genome) position: , mismatch: 7, identity: 0.788

ggactg--cgccgaccgcaacaccccgcccccggc	CRISPR spacer
--cctgaccaccgaccgcaacaccccgctccagga	Protospacer
   ***  *.******************.** ** 

113. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MT451982 (Streptomyces phage Cumberbatch, complete genome) position: , mismatch: 7, identity: 0.788

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
gtccgtgatcggccacctggagtggagttccga	Protospacer
*** ********************* . .* *.

114. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MT451980 (Streptomyces phage Ignacio, complete genome) position: , mismatch: 7, identity: 0.788

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
gtccgtgatcggccacctggagtggagttccga	Protospacer
*** ********************* . .* *.

115. spacer 20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 7, identity: 0.788

gtgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
aaggtcgccttccaggtcgatgtcggggtcgag	Protospacer
. * **  ****************** * ****

116. spacer 20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP045374 (Sulfitobacter sp. THAF37 plasmid pTHAF37_b, complete sequence) position: , mismatch: 7, identity: 0.788

gtgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
gccttccgcttccaggtcgatgacgtcgggaag	Protospacer
*. .****************** ** *** .**

117. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to CP027480 (Pseudomonas koreensis strain P19E3 plasmid p3, complete sequence) position: , mismatch: 7, identity: 0.788

gattgcggccgagctcggcgtcac--cttcggtga	CRISPR spacer
gattgcggccgagcacggcatcaccgcatcgcc--	Protospacer
************** ****.****  * *** .  

118. spacer 20.31|5740763|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP018064 (Rhodococcus sp. 2G plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.788

gtcggtactcgggtgactccggtcgaccacggt	CRISPR spacer
gtacgcgttcgggtgcatccggtcgaccacggt	Protospacer
**  *...*******  ****************

119. spacer 20.32|5740824|31|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022193 (Yangia pacifica strain YSBP01 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.774

gacgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
cgcgaggtgaacatgggcgtcgatgccgccc	Protospacer
 .**********.************   **.

120. spacer 20.32|5740824|31|NZ_CP010833|CRISPRCasFinder matches to NZ_CP020811 (Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.774

gacgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
gtcgacgtgaacgtggacgtcgatggttccg	Protospacer
* *** **********.********. .** 

121. spacer 20.32|5740824|31|NZ_CP010833|CRISPRCasFinder matches to NZ_CP011248 (Agrobacterium tumefaciens strain Ach5 plasmid pAt, complete sequence) position: , mismatch: 7, identity: 0.774

gacgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
aatgacatgaacgtgagcgtcgatgagaccg	Protospacer
.*.** .********.*********** ** 

122. spacer 20.32|5740824|31|NZ_CP010833|CRISPRCasFinder matches to NZ_CP032919 (Agrobacterium tumefaciens strain 15955 plasmid pAt15955, complete sequence) position: , mismatch: 7, identity: 0.774

gacgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
aatgacatgaacgtgagcgtcgatgagaccg	Protospacer
.*.** .********.*********** ** 

123. spacer 20.32|5740824|31|NZ_CP010833|CRISPRCasFinder matches to NZ_CP033029 (Agrobacterium tumefaciens strain A6 plasmid pAtA6, complete sequence) position: , mismatch: 7, identity: 0.774

gacgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
aatgacatgaacgtgagcgtcgatgagaccg	Protospacer
.*.** .********.*********** ** 

124. spacer 20.34|5740944|32|NZ_CP010833|CRISPRCasFinder matches to NZ_CP031166 (Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence) position: , mismatch: 7, identity: 0.781

ggcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
ggcatcgacgtcgtcgtgccccgcaccagggc	Protospacer
**** ****************.**   * *.*

125. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP012701 (Sphingopyxis macrogoltabida strain EY-1 isolate activated sludge plasmid 1, complete sequence) position: , mismatch: 7, identity: 0.781

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
tcagaccggcgccctcgacgcgccccgctggc	Protospacer
.* ************** **********. . 

126. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 7, identity: 0.781

cctgac--cggcgccctcgtcgcgccccgcctag	CRISPR spacer
--tggccacggcgccctcgtcgcgcagcgccgcg	Protospacer
  **.*  *****************  ****  *

127. spacer 20.42|5739416|32|NZ_CP010833|CRT matches to NZ_CP017947 (Bosea sp. Tri-49 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.781

agcgaggagaagcgcctcgcggagcaccgagc-	CRISPR spacer
cgcgaagcgaagcgcctcgcggag-gtcgcgct	Protospacer
 ****.* **************** ..** ** 

128. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 7, identity: 0.781

gactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
aactgcgccgagcgcaccaccccgccggaagc	Protospacer
.********** **** *********   .**

129. spacer 20.47|5739721|32|NZ_CP010833|CRT matches to NZ_AP018829 (Asticcacaulis excentricus strain M6 plasmid pASEM-1, complete sequence) position: , mismatch: 7, identity: 0.781

ttcacgggtgacgcgcggcgactgttcttcgg	CRISPR spacer
tttgtgcgtaacgcgcggcgactggtcttcag	Protospacer
**...* **.************** *****.*

130. spacer 20.50|5739904|32|NZ_CP010833|CRT matches to NZ_CP013109 (Sinorhizobium americanum strain CFNEI 73 plasmid B, complete sequence) position: , mismatch: 7, identity: 0.781

gccaaggtccgggagtgggcggccac----cctcgg	CRISPR spacer
ggcatggtccgggagtcggcggccacaagtcc----	Protospacer
* ** *********** *********    **    

131. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NZ_CP017422 (Arthrobacter sp. ZXY-2 plasmid pZXY21, complete sequence) position: , mismatch: 7, identity: 0.781

cccagcgcggccgagcccagtccggcccgcag-	CRISPR spacer
acaagcgcggcccagcccagtcctg-cggcggc	Protospacer
 * ********* ********** * * **.* 

132. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MT451982 (Streptomyces phage Cumberbatch, complete genome) position: , mismatch: 7, identity: 0.781

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tccgtgatcggccacctggagtggagttccga	Protospacer
** ********************* . .* *.

133. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MT451980 (Streptomyces phage Ignacio, complete genome) position: , mismatch: 7, identity: 0.781

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tccgtgatcggccacctggagtggagttccga	Protospacer
** ********************* . .* *.

134. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 7, identity: 0.781

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
tgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
  *..******** ** ************* *

135. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 7, identity: 0.781

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
tgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
  *..******** ** ************* *

136. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NC_008269 (Rhodococcus jostii RHA1 plasmid pRHL1, complete sequence) position: , mismatch: 7, identity: 0.781

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ggcgccggcatcggcggcctgcaactgggcct	Protospacer
* *. * *****.*****************  

137. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 7, identity: 0.781

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
tgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
  *..******** ** ************* *

138. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 7, identity: 0.781

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
tgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
  *..******** ** ************* *

139. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_CP045374 (Sulfitobacter sp. THAF37 plasmid pTHAF37_b, complete sequence) position: , mismatch: 7, identity: 0.781

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
ccttccgcttccaggtcgatgacgtcgggaag	Protospacer
. .****************** ** *** .**

140. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_CP037916 (Sphingomonas sp. AAP5 plasmid p32, complete sequence) position: , mismatch: 7, identity: 0.781

-tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
ctgatac-cttccaggtcgatgtggtcggcgca	Protospacer
 ** * * *************** * ***** .

141. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NC_019408 (Caulobacter phage CcrRogue, complete genome) position: , mismatch: 7, identity: 0.781

-tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
atgc-ccgcttcatggtcgatgtcggcgacatc	Protospacer
 *** *******  **************.*.  

142. spacer 20.61|5740581|32|NZ_CP010833|CRT matches to MT657333 (Microbacterium phage Casend, complete genome) position: , mismatch: 7, identity: 0.781

ttcgtctgcgaccggtgccatcgcgacatgcg	CRISPR spacer
ttcatctgcgaccggtgctatcgccatgtgat	Protospacer
***.**************.***** *..**  

143. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP016619 (Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.781

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
cttgcggccgagctcggcgccaccatcaggac	Protospacer
 ******************.**** **.* . 

144. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to MN428048 (Gordonia phage DobbysSock, complete genome) position: , mismatch: 7, identity: 0.781

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
cttctcaccgagctcggtgtcgccttcggtga	Protospacer
 ** . .**********.***.**********

145. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to CP027480 (Pseudomonas koreensis strain P19E3 plasmid p3, complete sequence) position: , mismatch: 7, identity: 0.781

attgcggccgagctcggcgtcac--cttcggtga	CRISPR spacer
attgcggccgagcacggcatcaccgcatcgcc--	Protospacer
************* ****.****  * *** .  

146. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP015867 (Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence) position: , mismatch: 7, identity: 0.781

attgcg---gccgagctcggcgtcaccttcggtga	CRISPR spacer
---gcgcacgccgagttcggcgtccccttcggcca	Protospacer
   ***   ******.******** *******. *

147. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP030263 (Ensifer adhaerens strain Corn53 plasmid AA, complete sequence) position: , mismatch: 7, identity: 0.781

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
atgtccgccgatctcggcgtcaccgtcggcgc	Protospacer
**  * ***** ************ ****.* 

148. spacer 20.64|5740764|32|NZ_CP010833|CRT matches to NZ_CP018064 (Rhodococcus sp. 2G plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.781

tcggtactcgggtgactccggtcgaccacggt	CRISPR spacer
tacgcgttcgggtgcatccggtcgaccacggt	Protospacer
*  *...*******  ****************

149. spacer 20.65|5740825|30|NZ_CP010833|CRT matches to NZ_CP020811 (Mycobacterium dioxanotrophicus strain PH-06 plasmid unnamed2, complete sequence) position: , mismatch: 7, identity: 0.767

acgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
tcgacgtgaacgtggacgtcgatggttccg	Protospacer
 *** **********.********. .** 

150. spacer 20.66|5740884|32|NZ_CP010833|CRT matches to CP054927 (Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.781

aggatcgggatcacggcgtgcattcctacgcc	CRISPR spacer
aggaccgggatcaccgcgtgcatcgcggtgcc	Protospacer
****.********* ********. * ..***

151. spacer 20.67|5740945|31|NZ_CP010833|CRT matches to NZ_CP031166 (Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence) position: , mismatch: 7, identity: 0.774

gcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
gcatcgacgtcgtcgtgccccgcaccagggc	Protospacer
*** ****************.**   * *.*

152. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccgggggcggaggcccgtgcggc	Protospacer
******** *************  . ..*

153. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022775 (Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

154. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NC_014310 (Ralstonia solanacearum PSI07 plasmid mpPSI07, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

155. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022762 (Ralstonia solanacearum strain T95 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

156. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccgggggcggaggcccgtgcggc	Protospacer
******** *************  . ..*

157. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP023017 (Ralstonia solanacearum strain SL3022 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggctga	Protospacer
******** * *************.  . 

158. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP014703 (Ralstonia solanacearum strain KACC 10722 plasmid, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

159. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022760 (Ralstonia solanacearum strain T98 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

160. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022789 (Ralstonia solanacearum strain SL3175 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

161. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022771 (Ralstonia solanacearum strain T51 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

162. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022777 (Ralstonia solanacearum strain T11 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

163. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022799 (Ralstonia solanacearum strain SL2064 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

164. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022764 (Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

165. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022797 (Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

166. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022758 (Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
gcggggccggcggcggaggccccggccga	Protospacer
******** * *************.  . 

167. spacer 23.1|6773828|29|NZ_CP010833|CRISPRCasFinder matches to MH744418 (Streptomyces phage JustBecause, complete genome) position: , mismatch: 7, identity: 0.759

gcggggcccggggcggaggccccgaaaac	CRISPR spacer
acggggcccccggcggaggccccgcaggg	Protospacer
.********  ************* *.. 

168. spacer 9.2|3636769|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NZ_CP029777 (Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.758

gtacctggcggccgtggacgcggtgcggaaggc	CRISPR spacer
ggccctggcgaccgtggacgccgtgcgcagcgt	Protospacer
*  *******.********** ***** *. *.

169. spacer 20.3|5739049|33|NZ_CP010833|CRISPRCasFinder matches to LN997845 (Streptomyces reticuli genome assembly TUE45, plasmid : IV) position: , mismatch: 8, identity: 0.758

gcaggaccgggcccgcgccaaggcccggaggaa	CRISPR spacer
ggcgcgcaaggcccgcgccaaggcccgctggaa	Protospacer
*  * .* .******************  ****

170. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NC_014007 (Sphingobium japonicum UT26S plasmid pCHQ1, complete sequence) position: , mismatch: 8, identity: 0.758

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
ggcaacgcggcgccctcgtcgtgcccagcctcg	Protospacer
* * .  **************.**** **** *

171. spacer 20.22|5740209|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MT451981 (Streptomyces phage Vondra, complete genome) position: , mismatch: 8, identity: 0.758

gtcggtgatcggccacctggagtggcagccggg	CRISPR spacer
gtccgtgattggccacctggagtggagttccga	Protospacer
*** *****.*************** . .* *.

172. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 8, identity: 0.758

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ctgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
   *..******** ** ************* *

173. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 8, identity: 0.758

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ctgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
   *..******** ** ************* *

174. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 8, identity: 0.758

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ctgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
   *..******** ** ************* *

175. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 8, identity: 0.758

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ctgcgaccgcatcaccgtcctgcaactgggccg	Protospacer
   *..******** ** ************* *

176. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MK310144 (Mycobacterium phage CicholasNage, complete genome) position: , mismatch: 8, identity: 0.758

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
gctcagccgcataagcggccttcaacggcccac	Protospacer
* ********** ******** **** *  *. 

177. spacer 20.28|5740580|33|NZ_CP010833|CRISPRCasFinder matches to MT657333 (Microbacterium phage Casend, complete genome) position: , mismatch: 8, identity: 0.758

gttcgtctgcgaccggtgccatcgcgacatgcg	CRISPR spacer
cttcatctgcgaccggtgctatcgccatgtgat	Protospacer
 ***.**************.***** *..**  

178. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP016619 (Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.758

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
acttgcggccgagctcggcgccaccatcaggac	Protospacer
. ******************.**** **.* . 

179. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to MN428048 (Gordonia phage DobbysSock, complete genome) position: , mismatch: 8, identity: 0.758

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ccttctcaccgagctcggtgtcgccttcggtga	Protospacer
  ** . .**********.***.**********

180. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_KX443388 (Rhodococcus hoagii strain PAM1216 plasmid pVAPA1216, complete sequence) position: , mismatch: 8, identity: 0.758

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggtcgcgcgcgagctcggcgtcaccttcgcccc	Protospacer
*.*.***  ******************** .  

181. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013256 (Kocuria flava strain HO-9041 plasmid 2, complete sequence) position: , mismatch: 8, identity: 0.758

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggacccggccgagatccgcgtcaccttcgccga	Protospacer
*. . ******** ** ************ .**

182. spacer 20.32|5740824|31|NZ_CP010833|CRISPRCasFinder matches to NZ_CP021082 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence) position: , mismatch: 8, identity: 0.742

gacgaggtgaacgtgggcgtcgatgagccct	CRISPR spacer
gactacgtgaacgtgggcgtcgacaccgcca	Protospacer
*** * *****************..   ** 

183. spacer 20.34|5740944|32|NZ_CP010833|CRISPRCasFinder matches to NZ_CP019585 (Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymA, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
gccaacgacgacgtcgtgctctgcccgctggt	Protospacer
* ******** ********.***** * .*..

184. spacer 20.34|5740944|32|NZ_CP010833|CRISPRCasFinder matches to NC_017324 (Sinorhizobium meliloti BL225C plasmid pSINMEB01, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
gccaacgacgacgtcgtgctctgcccgctggt	Protospacer
* ******** ********.***** * .*..

185. spacer 20.34|5740944|32|NZ_CP010833|CRISPRCasFinder matches to NZ_CP021827 (Sinorhizobium meliloti strain KH35c plasmid psymA, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
gccaacgacgacgtcgtgctctgcccgctggt	Protospacer
* ******** ********.***** * .*..

186. spacer 20.36|5739050|32|NZ_CP010833|CRT matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

caggaccgggcccgcgccaaggcccggaggaa	CRISPR spacer
ctggaccgggcccgcgccgaggcgcgggccgt	Protospacer
* ****************.**** ***.  . 

187. spacer 20.36|5739050|32|NZ_CP010833|CRT matches to LN997845 (Streptomyces reticuli genome assembly TUE45, plasmid : IV) position: , mismatch: 8, identity: 0.75

caggaccgggcccgcgccaaggcccggaggaa	CRISPR spacer
gcgcgcaaggcccgcgccaaggcccgctggaa	Protospacer
  * .* .******************  ****

188. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP013597 (Rhizobium sp. N741 plasmid pRspN741b, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
agaagccggcgccgtcgacgcgccccgccttg	Protospacer
   ..******** *** ************ *

189. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP013501 (Rhizobium esperanzae strain N561 plasmid pRspN561a, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
agaagccggcgccgtcgacgcgccccgccttg	Protospacer
   ..******** *** ************ *

190. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP013507 (Rhizobium sp. N1341 plasmid pRspN1341b, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
agaagccggcgccgtcgacgcgccccgccttg	Protospacer
   ..******** *** ************ *

191. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP013518 (Rhizobium sp. N113 plasmid pRspN113a, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
agaagccggcgccgtcgacgcgccccgccttg	Protospacer
   ..******** *** ************ *

192. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP013491 (Rhizobium sp. N6212 plasmid pRspN6212a, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
agaagccggcgccgtcgacgcgccccgccttg	Protospacer
   ..******** *** ************ *

193. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP013496 (Rhizobium sp. N621 plasmid pRspN621a, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
agaagccggcgccgtcgacgcgccccgccttg	Protospacer
   ..******** *** ************ *

194. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP013591 (Rhizobium sp. N871 plasmid pRspN871a, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
agaagccggcgccgtcgacgcgccccgccttg	Protospacer
   ..******** *** ************ *

195. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NC_014007 (Sphingobium japonicum UT26S plasmid pCHQ1, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gcaacgcggcgccctcgtcgtgcccagcctcg	Protospacer
 * .  **************.**** **** *

196. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP050082 (Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b4, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gcgcagcggcgccctcgtcgccacccgccagg	Protospacer
 *  * ***************  ****** .*

197. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NC_008384 (Rhizobium leguminosarum bv. viciae 3841 plasmid pRL11, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gcgcagcggcgccctcgtcgccacccgccagg	Protospacer
 *  * ***************  ****** .*

198. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP049732 (Rhizobium leguminosarum strain A1 plasmid pRL11, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gcgcagcggcgccctcgtcgccacccgccagg	Protospacer
 *  * ***************  ****** .*

199. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_LR134465 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence) position: , mismatch: 8, identity: 0.75

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cctgaccggcggcatcgtcgcgctgcacaccg	Protospacer
*********** * *********. *.* . *

200. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 8, identity: 0.75

gactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
cccctcgccgaccgcatcaccccgccccagaa	Protospacer
  *. *********** *********** *. 

201. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to GQ919031 (Streptomyces phage ZL12, complete genome) position: , mismatch: 8, identity: 0.75

gactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
cggcccaccgaccgcaacaccctgccgccggc	Protospacer
 . . *.***************.*** *****

202. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NZ_CP033583 (Streptomyces sp. ADI95-16 plasmid pADI95-16b, complete sequence) position: , mismatch: 8, identity: 0.75

gactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
gtacccaccgaccgcaacaccccggcccggga	Protospacer
*  . *.***************** *** ** 

203. spacer 20.46|5739660|32|NZ_CP010833|CRT matches to NZ_CP017077 (Novosphingobium resinovorum strain SA1 plasmid pSA2, complete sequence) position: , mismatch: 8, identity: 0.75

tgtcggagacgcagcccggcagctgctcgatg	CRISPR spacer
cgtcggagacgctgcccgtcagcttgccgttt	Protospacer
.*********** ***** *****  .** * 

204. spacer 20.50|5739904|32|NZ_CP010833|CRT matches to NZ_CP017947 (Bosea sp. Tri-49 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

gccaaggtccgggagtgggcggccaccctcgg	CRISPR spacer
gccaaggtccgggagcggtcggcggaattcga	Protospacer
***************.** **** .  .***.

205. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NZ_CP044425 (Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence) position: , mismatch: 8, identity: 0.75

cccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
tcgagcgcggccgagccaagcccggccttgac	Protospacer
.* ************** **.******.  * 

206. spacer 20.53|5740087|33|NZ_CP010833|CRT matches to MF417926 (Uncultured Caudovirales phage clone 9F_1, partial genome) position: , mismatch: 8, identity: 0.758

cggtccggggttcacctgatcacccccgccccc	CRISPR spacer
gtgtgcggggttcacctgttcaccccagttcac	Protospacer
  ** ************* ******* *..* *

207. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to MT451981 (Streptomyces phage Vondra, complete genome) position: , mismatch: 8, identity: 0.75

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
tccgtgattggccacctggagtggagttccga	Protospacer
** *****.*************** . .* *.

208. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 8, identity: 0.75

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ctggcccgcatcgtcggcctgcaactgggcaa	Protospacer
 * . *******. ****************..

209. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 8, identity: 0.75

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ctggcccgcatcgtcggcctgcaactgggcaa	Protospacer
 * . *******. ****************..

210. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to MK310144 (Mycobacterium phage CicholasNage, complete genome) position: , mismatch: 8, identity: 0.75

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ctcagccgcataagcggccttcaacggcccac	Protospacer
 ********** ******** **** *  *. 

211. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.75

-------tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
ttggagttg-------tccaggtcgatgtcggtggcgag	Protospacer
       **       ****************.******

212. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_CP023064 (Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence) position: , mismatch: 8, identity: 0.75

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
gcctccgcttccagatcgatgtcgtcgtgaac	Protospacer
  ************.********* **  .* 

213. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_CP047174 (Rathayibacter sp. VKM Ac-2760 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
tcttctcgctcctggccgatgtcggcggcgag	Protospacer
* .**.  .*** **.****************

214. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_CP015881 (Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence) position: , mismatch: 8, identity: 0.75

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
ttgccaacatcccggtcgttgtcggcggcgag	Protospacer
*  .* .* *** ***** *************

215. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_AP022607 (Mycobacterium branderi strain JCM 12687 plasmid pJCM12687) position: , mismatch: 8, identity: 0.75

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
gtcagcgagtcctggtcgatgttggcggcgag	Protospacer
  *  **  *** *********.*********

216. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_CP030263 (Ensifer adhaerens strain Corn53 plasmid AA, complete sequence) position: , mismatch: 8, identity: 0.75

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
ttgccaacatcccggtcgttgtcggcggcgag	Protospacer
*  .* .* *** ***** *************

217. spacer 20.58|5740393|32|NZ_CP010833|CRT matches to NZ_LR594692 (Variovorax sp. WDL1 plasmid 4) position: , mismatch: 8, identity: 0.75

gggttcgcataccggctgcgcgggccgacgta	CRISPR spacer
gtgttcgcgtacctgctgcgcgggctggccat	Protospacer
* ******.**** ***********.*.*   

218. spacer 20.60|5740520|32|NZ_CP010833|CRT matches to NC_011356 (Enterobacteria phage YYZ-2008, complete prophage genome) position: , mismatch: 8, identity: 0.75

caggtgatgggctccatcaacttgttcggggt	CRISPR spacer
cgggtgatgggcaccatcaaattgtatgaagc	Protospacer
*.********** ******* **** .*..*.

219. spacer 20.60|5740520|32|NZ_CP010833|CRT matches to FJ184280 (Enterobacteria phage YYZ-2008, complete genome) position: , mismatch: 8, identity: 0.75

caggtgatgggctccatcaacttgttcggggt	CRISPR spacer
cgggtgatgggcaccatcaaattgtatgaagc	Protospacer
*.********** ******* **** .*..*.

220. spacer 20.60|5740520|32|NZ_CP010833|CRT matches to AP000400 (Enterobacteria phage VT1-Sakai genomic DNA, prophage inserted region in Escherichia coli O157:H7) position: , mismatch: 8, identity: 0.75

caggtgatgggctccatcaacttgttcggggt	CRISPR spacer
cgggtgatgggcaccatcaaattgtatgaagc	Protospacer
*.********** ******* **** .*..*.

221. spacer 20.62|5740642|32|NZ_CP010833|CRT matches to NZ_CP016082 (Streptomyces sp. SAT1 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

tccgccattcccggaccgattgccgatgccct	CRISPR spacer
agcgtcccgcccggaccgctcgccgatgccct	Protospacer
  **.* . ********* *.***********

222. spacer 20.62|5740642|32|NZ_CP010833|CRT matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 8, identity: 0.75

tccgccattcccggaccgattgccgatgccct	CRISPR spacer
gccgccattcccggaccgaaggccagcgccag	Protospacer
 ******************  ***...***  

223. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_LR594660 (Variovorax sp. PBL-H6 plasmid 2) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggcctgcacgagctcggcgtcaccttgggtga	Protospacer
. . .*  ****************** *****

224. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_LR594667 (Variovorax sp. SRS16 plasmid 2) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggcctgcacgagctcggcgtcaccttgggtga	Protospacer
. . .*  ****************** *****

225. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_LR594690 (Variovorax sp. WDL1 plasmid 2) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggcctgcacgagctcggcgtcaccttgggtga	Protospacer
. . .*  ****************** *****

226. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_LR594672 (Variovorax sp. PBL-E5 plasmid 2) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggcctgcacgagctcggcgtcaccttgggtga	Protospacer
. . .*  ****************** *****

227. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_KX443388 (Rhodococcus hoagii strain PAM1216 plasmid pVAPA1216, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gtcgcgcgcgagctcggcgtcaccttcgcccc	Protospacer
.*.***  ******************** .  

228. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP050098 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
attgccgccgagctcggcgtcgccgcctcgaa	Protospacer
***** ***************.** .*   .*

229. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP013256 (Kocuria flava strain HO-9041 plasmid 2, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gacccggccgagatccgcgtcaccttcgccga	Protospacer
. . ******** ** ************ .**

230. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP053440 (Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
attgccgccgagctcggcgtcgccgcctcgaa	Protospacer
***** ***************.** .*   .*

231. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP006990 (Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga----	CRISPR spacer
atcgcggccgagctcggcgtc----tccaggacgct	Protospacer
**.******************    ** . **    

232. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NC_012848 (Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
attgccgccgagctcggcgtcgccgcctcaaa	Protospacer
***** ***************.** .*   .*

233. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to CP007644 (Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803c, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga----	CRISPR spacer
atcgcggccgagctcggcgtc----tccaggacgct	Protospacer
**.******************    ** . **    

234. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP018230 (Rhizobium leguminosarum strain Vaf-108 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggtgacgccgatatcggcgtcaccttcggcta	Protospacer
. **  *****  ****************. *

235. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP048282 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248d, complete sequence) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ggtgacgccgatatcggcgtcaccttcggcta	Protospacer
. **  *****  ****************. *

236. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to MH045567 (Microbacterium phage Elva, complete genome) position: , mismatch: 8, identity: 0.75

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
cttcgggccgagctccgcgtcgccttcgccca	Protospacer
 **  ********** *****.****** . *

237. spacer 20.67|5740945|31|NZ_CP010833|CRT matches to NZ_CP019585 (Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymA, complete sequence) position: , mismatch: 8, identity: 0.742

gcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
ccaacgacgacgtcgtgctctgcccgctggt	Protospacer
 ******** ********.***** * .*..

238. spacer 20.67|5740945|31|NZ_CP010833|CRT matches to NC_017324 (Sinorhizobium meliloti BL225C plasmid pSINMEB01, complete sequence) position: , mismatch: 8, identity: 0.742

gcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
ccaacgacgacgtcgtgctctgcccgctggt	Protospacer
 ******** ********.***** * .*..

239. spacer 20.67|5740945|31|NZ_CP010833|CRT matches to NZ_CP021827 (Sinorhizobium meliloti strain KH35c plasmid psymA, complete sequence) position: , mismatch: 8, identity: 0.742

gcaacgacgtcgtcgtgccctgccagacgac	CRISPR spacer
ccaacgacgacgtcgtgctctgcccgctggt	Protospacer
 ******** ********.***** * .*..

240. spacer 1.1|27001|34|NZ_CP010833|CRISPRCasFinder matches to NC_011273 (Mycobacterium phage Myrna, complete genome) position: , mismatch: 9, identity: 0.735

gtggccacccggaggccacggacaccgtgaccgg	CRISPR spacer
cggttgacccggaggacccggacaccgtgaccat	Protospacer
  * . ********* * **************. 

241. spacer 1.1|27001|34|NZ_CP010833|CRISPRCasFinder matches to NC_019957 (Mycobacterium sp. JS623 plasmid pMYCSM01, complete sequence) position: , mismatch: 9, identity: 0.735

gtggccacccggaggccacggacaccgtgaccgg	CRISPR spacer
acagccacccggtggccacggacagcgccagcgt	Protospacer
...********* *********** **. * ** 

242. spacer 9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NZ_CP041156 (Leisingera aquaemixtae strain R2C4 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.727

cgactccgtcgccgcggccgcagccagatcggg	CRISPR spacer
ttcatgcgtcgccgcggccgccgccggatcatg	Protospacer
.   * *************** ***.****. *

243. spacer 9.2|3636769|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to MT114163 (Mycobacterium phage Settecandela, complete genome) position: , mismatch: 9, identity: 0.727

gtacctggcggccgtggacgcggtgcggaaggc	CRISPR spacer
gtacctggcggcgctggacgcggtcgcgatcaa	Protospacer
************  **********   **  . 

244. spacer 9.2|3636769|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to MK937592 (Mycobacterium phage Phrappuccino, complete genome) position: , mismatch: 9, identity: 0.727

gtacctggcggccgtggacgcggtgcggaaggc	CRISPR spacer
gtacctggcggcgctggacgcggtcgcgatcaa	Protospacer
************  **********   **  . 

245. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP039693 (Agrobacterium larrymoorei strain CFBP5473 plasmid pAlCFBP5473, complete sequence) position: , mismatch: 9, identity: 0.735

-tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
ccacg-cccgccgccgccgcccgccgccttgatga	Protospacer
 ..** .*. ********  **************.

246. spacer 18.5|5047079|31|NZ_CP010833|CRT matches to NC_011366 (Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG202, complete sequence) position: , mismatch: 9, identity: 0.71

ctcgacgaccggcgagacgtccaccacgggt	CRISPR spacer
gcagacgaccagcgagacgaccaccacccag	Protospacer
 . *******.******** *******  . 

247. spacer 18.5|5047079|31|NZ_CP010833|CRT matches to NZ_CP035001 (Rhizobium acidisoli strain FH23 plasmid pRapFH23c, complete sequence) position: , mismatch: 9, identity: 0.71

ctcgacgaccggcgagacgtccaccacgggt	CRISPR spacer
gcagacgaccagcgagacgaccaccacccag	Protospacer
 . *******.******** *******  . 

248. spacer 18.5|5047079|31|NZ_CP010833|CRT matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 9, identity: 0.71

ctcgacgaccggcgagacgtccaccacgggt	CRISPR spacer
tcggacgaccggcgagacgttcatcaagaac	Protospacer
.. *****************.**.** *...

249. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013597 (Rhizobium sp. N741 plasmid pRspN741b, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cagaagccggcgccgtcgacgcgccccgccttg	Protospacer
    ..******** *** ************ *

250. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013501 (Rhizobium esperanzae strain N561 plasmid pRspN561a, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cagaagccggcgccgtcgacgcgccccgccttg	Protospacer
    ..******** *** ************ *

251. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013507 (Rhizobium sp. N1341 plasmid pRspN1341b, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cagaagccggcgccgtcgacgcgccccgccttg	Protospacer
    ..******** *** ************ *

252. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013518 (Rhizobium sp. N113 plasmid pRspN113a, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cagaagccggcgccgtcgacgcgccccgccttg	Protospacer
    ..******** *** ************ *

253. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013491 (Rhizobium sp. N6212 plasmid pRspN6212a, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cagaagccggcgccgtcgacgcgccccgccttg	Protospacer
    ..******** *** ************ *

254. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013496 (Rhizobium sp. N621 plasmid pRspN621a, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cagaagccggcgccgtcgacgcgccccgccttg	Protospacer
    ..******** *** ************ *

255. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP013591 (Rhizobium sp. N871 plasmid pRspN871a, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cagaagccggcgccgtcgacgcgccccgccttg	Protospacer
    ..******** *** ************ *

256. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP009216 (Corynebacterium ureicelerivorans strain IMMIB RIV-2301 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gacaccacggcccccacgtcgcgccccgcctgc	Protospacer
* *    **** *** ***************. 

257. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to GQ919031 (Streptomyces phage ZL12, complete genome) position: , mismatch: 9, identity: 0.727

ggactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
ccggcccaccgaccgcaacaccctgccgccggc	Protospacer
  . . *.***************.*** *****

258. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP007144 (Hymenobacter swuensis DY53 plasmid pHsw1, complete sequence) position: , mismatch: 9, identity: 0.727

ggactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
gaacagcgccgaccgcaccaccccgcgcgactt	Protospacer
*.** ************ ******** *    .

259. spacer 20.10|5739476|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP033583 (Streptomyces sp. ADI95-16 plasmid pADI95-16b, complete sequence) position: , mismatch: 9, identity: 0.727

ggactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
cgtacccaccgaccgcaacaccccggcccggga	Protospacer
 *  . *.***************** *** ** 

260. spacer 20.17|5739903|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MH001458 (Mycobacterium phage Smeagol, complete genome) position: , mismatch: 9, identity: 0.727

ggccaaggtccgggagtgggcggccaccctcgg	CRISPR spacer
gccgaagggccgggagtggtcggccaccgctct	Protospacer
* * **** ********** ******** ..  

261. spacer 20.19|5740025|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP044425 (Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence) position: , mismatch: 9, identity: 0.727

gcccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
atcgagcgcggccgagccaagcccggccttgac	Protospacer
..* ************** **.******.  * 

262. spacer 20.20|5740086|34|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to MF417926 (Uncultured Caudovirales phage clone 9F_1, partial genome) position: , mismatch: 9, identity: 0.735

gcggtccggggttcacctgatcacccccgccccc	CRISPR spacer
tgtgtgcggggttcacctgttcaccccagttcac	Protospacer
   ** ************* ******* *..* *

263. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 9, identity: 0.727

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
cctggcccgcatcgtcggcctgcaactgggcaa	Protospacer
  * . *******. ****************..

264. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.727

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
cctggcccgcatcgtcggcctgcaactgggcaa	Protospacer
  * . *******. ****************..

265. spacer 20.24|5740331|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP023064 (Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence) position: , mismatch: 9, identity: 0.727

gtgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
tgcctccgcttccagatcgatgtcgtcgtgaac	Protospacer
   ************.********* **  .* 

266. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to MK376956 (Gordonia phage WilliamBoone, complete genome) position: , mismatch: 9, identity: 0.727

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gattgccgacgagctcggcgtcacccagcccta	Protospacer
****** * ****************.    . *

267. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP050098 (Rhizobium leguminosarum bv. trifolii strain 9B plasmid pRL9b4, complete sequence) position: , mismatch: 9, identity: 0.727

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
cattgccgccgagctcggcgtcgccgcctcgaa	Protospacer
 ***** ***************.** .*   .*

268. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP053440 (Rhizobium leguminosarum bv. trifolii strain CC275e plasmid pRltCC275eF, complete sequence) position: , mismatch: 9, identity: 0.727

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
cattgccgccgagctcggcgtcgccgcctcgaa	Protospacer
 ***** ***************.** .*   .*

269. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP006990 (Rhizobium sp. IE4771 plasmid pRetIE4771d, complete sequence) position: , mismatch: 9, identity: 0.727

gattgcggccgagctcggcgtcaccttcggtga----	CRISPR spacer
tatcgcggccgagctcggcgtc----tccaggacgct	Protospacer
 **.******************    ** . **    

270. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NC_012848 (Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132501, complete sequence) position: , mismatch: 9, identity: 0.727

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
cattgccgccgagctcggcgtcgccgcctcaaa	Protospacer
 ***** ***************.** .*   .*

271. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to CP007644 (Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803c, complete sequence) position: , mismatch: 9, identity: 0.727

gattgcggccgagctcggcgtcaccttcggtga----	CRISPR spacer
tatcgcggccgagctcggcgtc----tccaggacgct	Protospacer
 **.******************    ** . **    

272. spacer 20.36|5739050|32|NZ_CP010833|CRT matches to NZ_CP041044 (Paracoccus sp. AK26 plasmid pAK2, complete sequence) position: , mismatch: 9, identity: 0.719

caggaccgggcccgcgccaaggcccggaggaa	CRISPR spacer
gaggaccggcgccgcgccaaggccctggctgc	Protospacer
 ********  ************** *.  . 

273. spacer 20.36|5739050|32|NZ_CP010833|CRT matches to NZ_CP045549 (Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.719

caggaccgggcccgcgccaaggcccggaggaa	CRISPR spacer
gggctccgggcccgcgccgaggaccggaccac	Protospacer
 .*  *************.*** *****  * 

274. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP009216 (Corynebacterium ureicelerivorans strain IMMIB RIV-2301 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.719

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
acaccacggcccccacgtcgcgccccgcctgc	Protospacer
 *    **** *** ***************. 

275. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to CP047137 (Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.719

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cctgaccgccgcccccgtcgcgccacaagcga	Protospacer
******** *****.********* *.  ...

276. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_LR134460 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 18, complete sequence) position: , mismatch: 9, identity: 0.719

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
ccgctccggcgccttcggcgcgccccgcgact	Protospacer
**   ********.*** **********    

277. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP016821 (Rhodococcus sp. p52 plasmid pDF01, complete sequence) position: , mismatch: 9, identity: 0.719

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
tccggccggcgccctcgccgcaccccgcagga	Protospacer
.*.*.************.***.******  ..

278. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP016822 (Rhodococcus sp. p52 plasmid pDF03, complete sequence) position: , mismatch: 9, identity: 0.719

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
tccggccggcgccctcgccgcaccccgcagga	Protospacer
.*.*.************.***.******  ..

279. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP016822 (Rhodococcus sp. p52 plasmid pDF03, complete sequence) position: , mismatch: 9, identity: 0.719

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
tccggccggcgccctcgccgcaccccgcagga	Protospacer
.*.*.************.***.******  ..

280. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to MT657335 (Gordonia phage Mariokart, complete genome) position: , mismatch: 9, identity: 0.719

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gatgaccggcgcccacggcgcgcccgacgggg	Protospacer
  ************ ** ******* .*  .*

281. spacer 20.39|5739233|32|NZ_CP010833|CRT matches to NZ_CP021355 (Rhodococcus sp. S2-17 plasmid pRB98, complete sequence) position: , mismatch: 9, identity: 0.719

gtccgacccgggccagctgaaagggagcgagg	CRISPR spacer
atcacctccgggtcagcggaaagggagcgatt	Protospacer
.**   .*****.**** ************  

282. spacer 20.42|5739416|32|NZ_CP010833|CRT matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 9, identity: 0.719

agcgaggagaagcgcctcgcggagcaccgagc	CRISPR spacer
gccgaggagaagcgcgtcgccgagcagcagcg	Protospacer
. ************* **** ***** *..  

283. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NZ_CP007144 (Hymenobacter swuensis DY53 plasmid pHsw1, complete sequence) position: , mismatch: 9, identity: 0.719

gactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
aacagcgccgaccgcaccaccccgcgcgactt	Protospacer
.** ************ ******** *    .

284. spacer 20.43|5739477|32|NZ_CP010833|CRT matches to NZ_CP034813 (Paracoccus sp. Arc7-R13 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.719

gactgcgccgaccgcaacaccccgcccccggc	CRISPR spacer
ggccagatcgaccgcatcaccccgcccgcggg	Protospacer
*.*.. ..******** ********** *** 

285. spacer 20.49|5739843|32|NZ_CP010833|CRT matches to NZ_AF135182 (Serratia entomophila strain A1MO2 plasmid pADAP, complete sequence) position: , mismatch: 9, identity: 0.719

gtctttctgacctggggcgtttcggtttctcc	CRISPR spacer
gcaccgcgaacccgggccgtttcggtttctcc	Protospacer
*. .. * .***.*** ***************

286. spacer 20.49|5739843|32|NZ_CP010833|CRT matches to NC_002523 (Serratia entomophila plasmid pADAP, complete sequence) position: , mismatch: 9, identity: 0.719

gtctttctgacctggggcgtttcggtttctcc	CRISPR spacer
gcaccgcgaacccgggccgtttcggtttctcc	Protospacer
*. .. * .***.*** ***************

287. spacer 20.50|5739904|32|NZ_CP010833|CRT matches to MH001458 (Mycobacterium phage Smeagol, complete genome) position: , mismatch: 9, identity: 0.719

gccaaggtccgggagtgggcggccaccctcgg	CRISPR spacer
ccgaagggccgggagtggtcggccaccgctct	Protospacer
 * **** ********** ******** ..  

288. spacer 20.50|5739904|32|NZ_CP010833|CRT matches to NZ_CP040819 (Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence) position: , mismatch: 9, identity: 0.719

gccaaggtccgggagtgggcggccaccctcgg	CRISPR spacer
gcggcggcccgggagcgggcggccaccccgtc	Protospacer
** . **.*******.************.   

289. spacer 20.50|5739904|32|NZ_CP010833|CRT matches to MN062714 (Microbacterium Phage DirtyBubble, complete genome) position: , mismatch: 9, identity: 0.719

gccaaggtccgggagtgggcggccaccctcgg	CRISPR spacer
agcgcggtccgcgactgggcggccaccccaga	Protospacer
. *. ****** ** *************. *.

290. spacer 20.50|5739904|32|NZ_CP010833|CRT matches to MT024860 (Microbacterium phage Stromboli, complete genome) position: , mismatch: 9, identity: 0.719

gccaaggtccgggagtgggcggccaccctcgg	CRISPR spacer
agcgcggtccgcgactgggcggccaccccaga	Protospacer
. *. ****** ** *************. *.

291. spacer 20.51|5739965|32|NZ_CP010833|CRT matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.719

aggctagacccggccacggtggaggccgcccg	CRISPR spacer
gtgcgcgacgcggccgcggtggaggccgcagc	Protospacer
. **  *** *****.*************   

292. spacer 20.51|5739965|32|NZ_CP010833|CRT matches to MT708545 (Rhizobium phage Pasto, complete genome) position: , mismatch: 9, identity: 0.719

aggctagacccggccacggtggaggccgcccg	CRISPR spacer
atcgttactccggccacgctggaggacgcccg	Protospacer
*   * . .********* ****** ******

293. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NZ_CP012940 (Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.719

cccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
gcgcgcgcggccgagtccattccggccgaccc	Protospacer
 *  ***********.*** ******* .*  

294. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NZ_CP012944 (Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.719

cccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
gcgcgcgcggccgagtccattccggccgaccc	Protospacer
 *  ***********.*** ******* .*  

295. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NC_017575 (Ralstonia solanacearum Po82 megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.719

cccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
gcgcgcgcggccgagtccattccggccgaccc	Protospacer
 *  ***********.*** ******* .*  

296. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NZ_CP026308 (Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.719

cccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
gcgcgcgcggccgagtccattccggccgaccc	Protospacer
 *  ***********.*** ******* .*  

297. spacer 20.52|5740026|32|NZ_CP010833|CRT matches to NZ_CP051295 (Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.719

cccagcgcggccgagcccagtccggcccgcag	CRISPR spacer
gcgcgcgcggccgagtccattccggccgaccc	Protospacer
 *  ***********.*** ******* .*  

298. spacer 20.55|5740210|32|NZ_CP010833|CRT matches to NZ_CP040819 (Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence) position: , mismatch: 9, identity: 0.719

tcggtgatcggccacctggagtggcagccggg	CRISPR spacer
caggtgatcggccacctggcggggctggggca	Protospacer
. ***************** * *** *  * .

299. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_LN831788 (Streptomyces leeuwenhoekii strain type strain (C34 = DSM 42122 = NRRL B-24963) plasmid pSLE1, complete sequence) position: , mismatch: 9, identity: 0.719

tgctccg----cttccaggtcgatgtcggcggcgag	CRISPR spacer
----tcgaagtcttcggggtcgatgtcggcggcgcc	Protospacer
    .**    **** .*****************  

300. spacer 20.61|5740581|32|NZ_CP010833|CRT matches to NZ_CP020331 (Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgtctgcgaccggtgccatcgcgacatgcg	CRISPR spacer
cgggcaggcgaccggcgccatcgtgacatgtg	Protospacer
.  *.  ********.*******.******.*

301. spacer 20.61|5740581|32|NZ_CP010833|CRT matches to NZ_CP046574 (Rhodococcus sp. WAY2 plasmid pRWAY02, complete sequence) position: , mismatch: 9, identity: 0.719

ttcgtctgcgaccggtgccatcgcgacatgcg	CRISPR spacer
ctcggctgcgaccggtgcgatcgccctcgtcg	Protospacer
.*** ************* *****  .   **

302. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to MK376956 (Gordonia phage WilliamBoone, complete genome) position: , mismatch: 9, identity: 0.719

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
attgccgacgagctcggcgtcacccagcccta	Protospacer
***** * ****************.    . *

303. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP020897 (Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5a, complete sequence) position: , mismatch: 9, identity: 0.719

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gaactggccgagctcggcatccccttcgccga	Protospacer
.   .*************.** ****** .**

304. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP022191 (Yangia pacifica strain YSBP01 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
cttgcggccgagatcgtcgtcaccagcccgca	Protospacer
 *********** *** *******  *    *

305. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP029209 (Nitratireductor sp. OM-1 plasmid pOM-1, complete sequence) position: , mismatch: 9, identity: 0.719

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
caggaggccgaactcggcttcaccttcgacta	Protospacer
   * ******.****** *********.. *

306. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP054615 (Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
ctctacgccctgctcggcgtcaccttcggcgg	Protospacer
 *.   ***  ******************.*.

307. spacer 20.66|5740884|32|NZ_CP010833|CRT matches to NC_014533 (Gloeothece verrucosa PCC 7822 plasmid Cy782201, complete sequence) position: , mismatch: 9, identity: 0.719

aggatcgggatcacggcgtgcattcctacgcc	CRISPR spacer
ggctacatcatcacgccgggcattcctacgcc	Protospacer
.*   *.  ****** ** *************

308. spacer 9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NC_007766 (Rhizobium etli CFN 42 plasmid p42f, complete sequence) position: , mismatch: 10, identity: 0.697

cgactccgtcgccgcggccgcagccagatcggg	CRISPR spacer
tgggctcgtcgccgcggctgccgccagatctct	Protospacer
.*. ..************.** ********   

309. spacer 18.2|5046890|37|NZ_CP010833|CRT matches to AF440695 (Virus PhiCh1, complete genome) position: , mismatch: 10, identity: 0.73

cacgaccggtgagaccacgggcgagacgtccaccacg	CRISPR spacer
ggcgaccggagagaccaccggcgagacgatgaccgtc	Protospacer
 .******* ******** ********* . ***.. 

310. spacer 18.2|5046890|37|NZ_CP010833|CRT matches to NC_004084 (Natrialba phage PhiCh1, complete genome) position: , mismatch: 10, identity: 0.73

cacgaccggtgagaccacgggcgagacgtccaccacg	CRISPR spacer
ggcgaccggagagaccaccggcgagacgatgaccgtc	Protospacer
 .******* ******** ********* . ***.. 

311. spacer 20.3|5739049|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP041044 (Paracoccus sp. AK26 plasmid pAK2, complete sequence) position: , mismatch: 10, identity: 0.697

gcaggaccgggcccgcgccaaggcccggaggaa	CRISPR spacer
cgaggaccggcgccgcgccaaggccctggctgc	Protospacer
  ********  ************** *.  . 

312. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to CP047137 (Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.697

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
ccctgaccgccgcccccgtcgcgccacaagcga	Protospacer
 ******** *****.********* *.  ...

313. spacer 20.5|5739171|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 10, identity: 0.697

gcctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
gcctgcccggcgccctcggcgcgctgatcgaga	Protospacer
***** ************ *****.   *  ..

314. spacer 20.9|5739415|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 10, identity: 0.697

gagcgaggagaagcgcctcgcggagcaccgagc	CRISPR spacer
cgccgaggagaagcgcgtcgccgagcagcagcg	Protospacer
 . ************* **** ***** *..  

315. spacer 20.23|5740270|33|NZ_CP010833|CRISPRCasFinder,PILER-CR matches to NC_008712 (Paenarthrobacter aurescens TC1 plasmid pTC1, complete sequence) position: , mismatch: 10, identity: 0.697

ggtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
ggtcagccgcctcagcgccctgcactccgcata	Protospacer
********** ****** ****** .. *   .

316. spacer 20.30|5740702|33|NZ_CP010833|CRISPRCasFinder matches to NZ_CP025549 (Mycobacterium paragordonae strain 49061 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.697

gattgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gatcgcggccgagttcggcgtcacccggcccac	Protospacer
***.*********.***********.    .. 

317. spacer 20.36|5739050|32|NZ_CP010833|CRT matches to NZ_CP029362 (Streptomyces globisporus strain TFH56 plasmid pTFSG1, complete sequence) position: , mismatch: 10, identity: 0.688

caggaccgggcccgcgccaaggcccggaggaa	CRISPR spacer
cgtgaccgggtccgcgccgaggcccgtgccgc	Protospacer
*. *******.*******.******* .  . 

318. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP021653 (Ralstonia solanacearum strain RS 488 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
actgaccgccgcccccgtcgcgccacaagcga	Protospacer
 ******* *****.********* *.  ...

319. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP022366 (Azospirillum sp. TSH58 plasmid TSH58_p04, complete sequence) position: , mismatch: 10, identity: 0.688

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cctgcccggcgccctcggcgcgctgatcgaga	Protospacer
**** ************ *****.   *  ..

320. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP012688 (Ralstonia solanacearum strain UY031 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
actgaccgccgcccccgtcgcgccacaagcga	Protospacer
 ******* *****.********* *.  ...

321. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to CP047139 (Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
actgaccgccgcccccgtcgcgccacaagcga	Protospacer
 ******* *****.********* *.  ...

322. spacer 20.46|5739660|32|NZ_CP010833|CRT matches to MK967383 (Gordonia phage SweatNTears, complete genome) position: , mismatch: 10, identity: 0.688

tgtcggagacgcagcccggcagctgctcgatg	CRISPR spacer
atgcggagacgcagctcggcagcagccttgta	Protospacer
   ************.******* **.. .*.

323. spacer 20.49|5739843|32|NZ_CP010833|CRT matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 10, identity: 0.688

gtctttctgacctggggcgtttcggtttctcc	CRISPR spacer
agggccgtgaactggcgcgtttcggtttctgc	Protospacer
.   .. *** **** ************** *

324. spacer 20.50|5739904|32|NZ_CP010833|CRT matches to KF493880 (Mycobacterium phage HanShotFirst, complete genome) position: , mismatch: 10, identity: 0.688

gccaaggtccgggagtgggcggccaccctcgg	CRISPR spacer
ccgcagggccgggagtggtcggccaccgcgct	Protospacer
 *  *** ********** ******** .   

325. spacer 20.51|5739965|32|NZ_CP010833|CRT matches to NZ_CP039632 (Pseudomonas veronii strain Pvy plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.688

aggctagacccggccacggtggaggccgcccg	CRISPR spacer
ctggccgacccggccacggcagaggccgctga	Protospacer
  * . *************..********. .

326. spacer 20.51|5739965|32|NZ_CP010833|CRT matches to NC_014918 (Mesorhizobium ciceri biovar biserrulae WSM1271 plasmid pMESCI01, complete sequence) position: , mismatch: 10, identity: 0.688

aggctagacccggccacggtggaggccgcccg	CRISPR spacer
gctccgcgaccggccacggtgaaggcggcccg	Protospacer
.  *.. . ************.**** *****

327. spacer 20.56|5740271|32|NZ_CP010833|CRT matches to NC_008712 (Paenarthrobacter aurescens TC1 plasmid pTC1, complete sequence) position: , mismatch: 10, identity: 0.688

gtcagccgcatcagcggcctgcaactgggcgg	CRISPR spacer
gtcagccgcctcagcgccctgcactccgcata	Protospacer
********* ****** ****** .. *   .

328. spacer 20.57|5740332|32|NZ_CP010833|CRT matches to NZ_LR594673 (Variovorax sp. PBL-E5 plasmid 3) position: , mismatch: 10, identity: 0.688

tgctccgcttccaggtcgatgtcggcggcgag	CRISPR spacer
tcgagcgcttccagcccgatgtcggcgggctc	Protospacer
*    ********* .************    

329. spacer 20.58|5740393|32|NZ_CP010833|CRT matches to NZ_CP048421 (Sphingomonas insulae strain KCTC 12872 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.688

gggttcgcataccggctgcgcgggccgacgta	CRISPR spacer
tcgttcgcataccggcagcccgggcgcgctgg	Protospacer
  ************** ** *****  .*  .

330. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP025549 (Mycobacterium paragordonae strain 49061 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.688

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
atcgcggccgagttcggcgtcacccggcccac	Protospacer
**.*********.***********.    .. 

331. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NC_012586 (Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence) position: , mismatch: 10, identity: 0.688

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gtgttcgccgagcgcggcgtcaccgtcggaac	Protospacer
.*  . ******* ********** **** . 

332. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NC_023497 (Amycolatopsis keratiniphila plasmid pXL100, complete sequence) position: , mismatch: 10, identity: 0.688

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gcacacgccgagctgggcggcaccttcggcaa	Protospacer
..    ******** **** *********..*

333. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP023068 (Ensifer sojae CCBAU 05684 plasmid pSJ05684b, complete sequence) position: , mismatch: 10, identity: 0.688

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gtgttcgccgagcgcggcgtcaccgtcggaac	Protospacer
.*  . ******* ********** **** . 

334. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NC_011758 (Methylorubrum extorquens CM4 plasmid pCMU01, complete sequence) position: , mismatch: 10, identity: 0.688

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gacatggccgacctcggcgtcaccatcgccgg	Protospacer
. ...****** ************ *** .*.

335. spacer 20.63|5740703|32|NZ_CP010833|CRT matches to NZ_CP045549 (Streptomyces sp. SYP-A7193 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.688

attgcggccgagctcggcgtcaccttcggtga	CRISPR spacer
gcccacgccgagttcggcgtccccttcggcaa	Protospacer
...   ******.******** *******..*

336. spacer 9.1|3636708|33|NZ_CP010833|PILER-CR,CRISPRCasFinder matches to NC_021911 (Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1f, complete sequence) position: , mismatch: 11, identity: 0.667

cgactccgtcgccgcggccgcagccagatcggg	CRISPR spacer
ttggctcgtcgccgcggctgccgccagatctct	Protospacer
. . ..************.** ********   

337. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP043441 (Cupriavidus campinensis strain MJ1 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
atccccagcccgccgcgcagcgccgccttgatgc	Protospacer
  * ..  .******* ** ************* 

338. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NZ_CP035092 (Paracoccus denitrificans strain ATCC 19367 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.656

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cctgaacggcgcccccgtcgcgctttatgcca	Protospacer
***** ********.********..... . .

339. spacer 20.38|5739172|32|NZ_CP010833|CRT matches to NC_008688 (Paracoccus denitrificans PD1222 plasmid 1, complete sequence) position: , mismatch: 11, identity: 0.656

cctgaccggcgccctcgtcgcgccccgcctag	CRISPR spacer
cctgaacggcgcccccgtcgcgctttatgcca	Protospacer
***** ********.********..... . .

340. spacer 20.41|5739355|32|NZ_CP010833|CRT matches to NZ_CP016763 (Citrobacter freundii strain B38 plasmid pOZ172, complete sequence) position: , mismatch: 11, identity: 0.656

gccggtttgtcgctgatccaccggtagaccag	CRISPR spacer
tggcattcgtcgctgatccaccggcagatggc	Protospacer
    .**.****************.***. . 

341. spacer 20.41|5739355|32|NZ_CP010833|CRT matches to NZ_KX839208 (Klebsiella pneumoniae strain KP1814 plasmid pKP1814-2, complete sequence) position: , mismatch: 11, identity: 0.656

gccggtttgtcgctgatccaccggtagaccag	CRISPR spacer
tggcattcgtcgctgatccaccggcagatggc	Protospacer
    .**.****************.***. . 

342. spacer 20.41|5739355|32|NZ_CP010833|CRT matches to CP052526 (Klebsiella pneumoniae strain B16KP0177 plasmid pB16KP0177-2, complete sequence) position: , mismatch: 11, identity: 0.656

gccggtttgtcgctgatccaccggtagaccag	CRISPR spacer
tggcattcgtcgctgatccaccggcagatggc	Protospacer
    .**.****************.***. . 

343. spacer 20.41|5739355|32|NZ_CP010833|CRT matches to NZ_CP017991 (Enterobacter cloacae complex sp. ECNIH7 plasmid pENT-1ac, complete sequence) position: , mismatch: 11, identity: 0.656

gccggtttgtcgctgatccaccggtagaccag	CRISPR spacer
tggcattcgtcgctgatccaccggcagatggc	Protospacer
    .**.****************.***. . 

344. spacer 20.46|5739660|32|NZ_CP010833|CRT matches to NC_017643 (Escherichia coli UMNK88 plasmid pUMNK88_Hly, complete sequence) position: , mismatch: 11, identity: 0.656

tgtcggagacgcagcccggcagctgctcgatg	CRISPR spacer
cagtggtgacgcagcccgccagctgctgacca	Protospacer
.. .** *********** ******** . ..

345. spacer 20.47|5739721|32|NZ_CP010833|CRT matches to NZ_LT900339 (Gluconobacter oxydans 621H isolate WT-DSMZ plasmid 2) position: , mismatch: 11, identity: 0.656

ttcacgggtgacgcgcggcgactgttcttcgg	CRISPR spacer
ggaacgggtgacccgcagcgactgttgcgata	Protospacer
   ********* ***.********* .   .

346. spacer 20.47|5739721|32|NZ_CP010833|CRT matches to NC_006672 (Gluconobacter oxydans 621H plasmid pGOX1, complete sequence) position: , mismatch: 11, identity: 0.656

ttcacgggtgacgcgcggcgactgttcttcgg	CRISPR spacer
ggaacgggtgacccgcagcgactgttgcgata	Protospacer
   ********* ***.********* .   .

347. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 12, identity: 0.647

tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
cagaacaggtcgccgcgcaccgcccccttgatgg	Protospacer
.. . .   .****** ******* *********

348. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 12, identity: 0.647

tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
cagaacaggtcgccgcgcaccgcccccttgatgg	Protospacer
.. . .   .****** ******* *********

349. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 12, identity: 0.647

tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
cagaacaggtcgccgcgcaccgcccccttgatgg	Protospacer
.. . .   .****** ******* *********

350. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 12, identity: 0.647

tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
cagaacaggtcgccgcgcaccgcccccttgatgg	Protospacer
.. . .   .****** ******* *********

351. spacer 13.1|4698750|34|NZ_CP010833|CRISPRCasFinder matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 12, identity: 0.647

tgcgttcttccgccgcccaccgccgccttgatgg	CRISPR spacer
cagaacaggtcgccgcgcaccgcccccttgatgg	Protospacer
.. . .   .****** ******* *********

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	2178113 : 2203908	20	Sulfolobus_virus(25.0%)	plate,protease,tail	NA
DBSCAN-SWA_2	6465732 : 6472579	8	Streptomyces_phage(33.33%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP010833|2178113:2203908|DBSCAN-SWA
CGTGCGCAACACACGTAAATTCAGCCTTGCCGCCGCGGGCGTCCTGCTCTCGGCCGCCACGGTTCTGGGAACCCAGAGCATGGCCCAGGCGCAGGACGGGGCGGCCACTCCCCGCTACCAGCCCGAGATGGTCGAGGCGTTGGCCGCTTCGCTCGGCGTGAGCGAGAAGGCCGCGGTCGACCGGCTGGACCGGCAGGACGCCCAGCAGGCCAAGCTCGCCGGCCTCCAGAAGCGCGGCATATCCGGCGACGGGGCGTTCTTCGACGCCTCGGGCCGGCTGACCGTCAACGCCGACGACCACGCCGAGGCGGCCCGGATCGAGCAGGCCGGCCTCGACGCCCGCGTGCCCGCCAGAGGCCAGGCCGCCCTGGACAGAATCAAGGCCGAGCTGGACCGGCTCGCCGCCGCCACGACCCCCTCCGGTGTGGTCGCCTGGTCCGTGGACCTGCCCTCCGACCAGGTGACCGTCAAGGTCAACAACGAACGGGGAGCCGCCGCCAAGGCGTTCCTCGCCAAGGCCGCCGAGCACGGCTCCGCCGTCCGGATCGTGCGGGGCGAGGAGAAGCTGGAGGCCAAGGCCGCGATCTATCCCGGCAGCAAGATGACGTTCAACAACACCACCCAGTGGTGCTCCGTCGGCTACGGCGCCCGCGACAGCTCCGGCAGGCAGTACCTGGTGACCGCCGGGCACTGCGTCACGAACACCCTGCGCTACGACGGGGCGGCCTTCGCCCAGGGCTACAAGACCCGGTACGCGCTCGGCACCCGCAGTGTCGACATGGGCATCCTGACCATCAACTCCGGCCACTCGATCACCACCAGCGTCGGCACCTGGGGGAACAGCAACCCGGTCGCCGTCCGGGGCGGCACCCGCGCCTCGTCCGGCGCCGCGGTCTGCAAGTCCGGCGCCACCACCGGCTGGACCTGCGGCACGATCGGCTCGTACAACAACACCGTCACCTACGTCGACCTCAACGGCGGCCCCGACACGGTCGTCAGCGGCCTGGCCACCTCCAGCGTCTGCGTCGAGGGCGGCGACAGCGGCGGCGCGTACATCTCCGGCAACCAGGCCCAGGGCATGACCTCGGGCGGCCCGACCAACCAGCGCTGCACCGGCGGGGTCAACTCGCGCGGCTCCTCGTACTTCCAGCCGCTCGACGACACCCTCCGCTACTACGGGCTGACGCTCAACACCAACTAGGCACCGACCAGCACCACGGAGTACTCCCCGCAGAGAACCGGCCGGGGGCCGCTCGCGCGACCAGGCGAGCGGCCCCCGGTCGCGTCCCACGCACCATTTCGGGACAAAACATCCAATATATTGCTAGCTTTCCCTGGTTGGCCGATGACCGCATCGACGAGGGAACCCATGAGCCACCCCGAGGCCCCGCCCCGACCGGCCGCCAAACTGTCGCTCCTGACCCTGACCGCGATGGTGGTCGGTTCGATGGTCGGGGCCGGAGTCTTCTCGCTGCCCAGTCGGTTCGCGCAGGAGACCGGGGTCGCGGGGGCCCTGATCGCCTGGGCGGTCGCCGGGACGGGCATGCTGATGCTCGCCTTCGTCTTCCAGGCGCTCGCCGTGCGGCGGCCGGACCTGGACGCCGGGGTCTACGCGTACGCGAAGGCGGGGTTCGGCGAGTATCTCGGCTTCTTCTCGGCGTTCGGCTACTGGGCCAGCGCCTGCGTCGGCAATGTCACCTACTGGGTGCTCATCATGTCGACGGTCGGCGCGGTGGCGCCGGTGCTGGGCGACGGCGACACGGTGACGGCGGTGGTGGTCTCCTCGGTGGGGCTGTGGGGGTTCTTCCTGCTGATCCGGCGAGGCGTGAAGGAGGCGGCGGCGATCAACCGGATCGTCACCGTCGCGAAGGTCGTGCCGATCCTCTTCTTCGTCGTGCTGGCGCTCTTCTGCTTCGAACCGTCCGTCTTCGCCGACAACTTCAGCGGGACCGCCGAGGCGGGCACCCTCTTCGACCAGGTCCGGGGCACCATGCTCGCGACCGTCTTCGTGTTCCTCGGCGTCGAGGGGGCCAGCGTGTACTCGCGGCACGCCAAGCGCCGCGAGGACGTCGGCCGGGCCACCGTTCTGGGCTTCCTGAGCGTGTTCGCCGTCTTCGCGTCCGTCACGATCGTCAGTTACGGGCTGCTGCCGATGGCCGAGATCGCCGAGCTGCGGCAGCCGTCGATGGCCGGGGTTCTGGCGTCGGCCGTCGGGACGTGGGGGAAGGTCTTCATCAGCGTCGGCCTCGTCGTCTCCGTGCTCGGCGCCTACCTGGCCTGGACCCTGATGGCCGCCGAGGTCCTCTTCGTCGCCGCCCGGGACAAGGACATGCCGCGCTTCCTCGGGCAGTCGACCGCGGCGGACGTGCCCGAGAACGCGCTGCTCCTGACCACGTGCCTGAGCCAGCTCGTGCTCGTCGTGACGCTCTTCTCCGACGACGCGTTCGCCTTCGCCCTCGATCTGACCAGCGCACTGAGCCTGATCCCGTTCCTGCTGGCCGCCGCCTTCGCGGTGAAGGTCGCGGCCCGGCCCGAGCGCTGGGGTGCCGTGGGCCGCTCCGCCCGCCGTGAGCTGGTCATCGCCGTCGTGGCGACGCTGTACACCGCTTTCCTGCTGTACGCGGCCGGGCCGAAGTTCGTCCTCGTCTCCTTCATCCTCTACGCCCCGGCGACCTTCCTCTTCGTCAAGTCCCGCCGGGAGCAAGGCCGCCGGGTCTTCTCCCCCGGCGAAGCGGTCATCTGCGCGGTGTCGGTGGCGGGTGCCGCCGTCGGCATCGCGGCGCTGGCCCTCGGGTGGATCGAGCTGTGAGCACCGACCCCGTACCGGGTAGCGGACAGAACCCCGACGCACCGAGTGAAAGGCCCACCGTGACACCCACCGAGCCCGCTTCCGCCCTCGGCGTCCACTCCGAAGTGGGGCGGCTGCGCAAGGTCCTGGTCTGCGCCCCCGGCATGGCCCACCGCCGGCTGACCCCGACCAACTCCGACGATCTGCTCTTCGACGACGTGATGTGGGTGGAGAACGCCCAGCGGGACCATGCCGACTTCGTCAACCAGCTCACCGAGCGCGGGGTGGAGGTCGTCGAACTGCACGCGCTGCTCGCCGCCACCATGGAGATCCCGGAGGCCAGAACCTGGCTGCTCGACCGGAAGATCGACGCGAACGAGGTGGGTCTCGGGCTGGTCGACGACACCCGGGCCTTCCTCGATGCGCTGACGCCGCGCCGGCTGTCCGACCATCTCATCGGCGGGCTGGCCATCGCGGATCTGCCGGAGGAATTCCGTTCGGCGTACGTGGGTCTCGCCCGGGAGGGCACGGGGGCGCGGGAGTATCTGATGCCGCCGCTGCCCAACACGCTCTACACCCGGGACACCACCTGCTGGCTCTACAGCGGGGTGACGCTCAACCCGCTGTACTGGCCGGCCCGGCACGACGAGACCCTGCTGATGAAGGCGGTCTACACCTTCCACCCCGACTTCCGGGGCTCCAGGATCTGGTGGGGCGACCCGGAGAAGGACTGGGGCCGGGCCACGTTCGAGGGCGGGGACATCATGCCGGTCGGCAACGGTGTCGTCCTCATGGGGATGAGCGAACGAACCTCCCGACAGGCGATCACCCAGGTCGCGGCGGCCCTGTTCGCGCAGGGTGCCGCCGAGCACGTCATCGTCGCCGGAATGCCGAAGCTGCGTTCGGCCATGCACCTCGACACGGTGTTCACCTTCGCCGACCGGGACATCGTCACGCTGTACCCGCGCATCATGGACGCCGTCCACACGTTCTCACTGCGGCCGTCCGACCGGGCGCCCGGGATCGAGATCACCGACGAGGGATCGACACCGTTCACCGAGGTCGTGGCCCGGGCCCTGGGCCTGCCCCAGCTGCGGGTGATCGAGACGGGCGGCGACGTCTACGCCTCCGAGCGCCAGCAGTGGGACAGCGGCAACAACGCGGTGGCCCTGGAGCCGGGCGTCGTCTTCACCTACGACCGGAACACCCAGACGAACGCGCTGCTGCGGCGGGCCGGGGTGGAGGTCATCACGATCGTCGGCGCGGAGCTGGGGCGGGGCCGGGGCGGCGGGCACTGCATGACCTGCCCGCTGATCCGCGACGCGGTGGCGTTCTGACGGTGTACGGGCACGGGCCCGGATCCGCTTGGGGCGCGGGCCCCCGGATCAGTACCGCGCGAGCTACCGCCCGGCGCGGGCCCCGCACCCGTACGGGCTACCGCCCCGCGCGCGCCCGCTCCTTCGCCAGCCACGGGCCGAACTCGCTCTCCAGCACCAGCCGCCCCAGCTTGCGGTACTCCTGGAGTACCGCCGTGACGAGCTGGTCCATGGTCAGCGGGGCCCTCGACTCCGCCGCGAGGTAGGCGGCGGTCACCGCGCAGGCCCGGATCGAGCCGCCCGCCAGCTCGAAGCGGTCCGCGCAGAACTCCAGGTCGAGCGTGGCGTCGCGCGGGACCGCCGGGCCCAGGCAGCGGTCCCACAGGGCGAGGCGCTGGCGGGCGTCGGGCATCGGGAACTCGGCGATCACATCGAGGCGGCGGGTGAACGCCTCGTCGAGGTTGGCCCGGAGGTTGGTGGTGAGCACGGCGATGCCGTCGAAGGACTCCATGCGCTGGAGGAGATAGGCCGACTCCATGTTGGCGTGCTTGTCGCGGGAGTCGTTCACCTGGGAGCGCTTGCCGAAGATCGCGTCGGCCTCGTCGAACAGCAGGATGCCGTTGACGTCGGACGCCTCGACGAAGATGCGCTCCAGGTTCTTCTCGGTCTCCCCGATGTACTTGTCGACCACCGTGGACAGGTCCACGACGTACAGCTCCATGCCCAGTTCGGCGGCGACCACTTCGGCGGACATCGTCTTTCCCGTGCCGGACTCCCCGGCGAACAGGGCGATGACGCCTCTCCCCCGGCCGCCGCCCGGCCGCATCCGCCACTGCCCGAGGACCGTCTCGCGGTGGCGGGCGCGCAGGGCGAGTTCCGTGAGCTGGGTACGGGTGGAGGGGGGCAGCACCAGGTCGGCCCAGCCGACGCCGGGCTCGATGCGGCGGGCGAGCCGTTCCAGGCCCGCGCCGTTCTGGGCGCGGACCGCCGCCCGCAGGTCCTCCGGGCTGACCGGGCGGGGCTCCAGGACGGCCAGCCGGGAGGCTACGGTCGCGGCCCGGCGCAGCTGTCCGGAGTCGAGCCGGTAGGCGGCGGCAGCCTCGACGAGCGCGTCCCCGGCGGTGGCGTGCGCGGCGGACAGCCCGACCGAGCGGCCCGCTTCGGCGAGCGCCCGCCGCCACTGCCGCGCCATGCCGTCGGGGCCGGGCGGCGGGACGGTGACGGGCACCGGGCTCTCCGCGGTCCACAGCGGGTCCCAGTTCTTCTTCCCGTACGCGATCAGGGGCGTGGAGCCGAGCGCCGCGCACAGGGACCCGAGCAGCCGGGCCCCCTCGGGGCGTTCGGGGGCGAGCGTTTCGAGCGGGCCGAGGACGACACCGGCCCGGCCGAGACGGGACTCCGTCGCCAACGCCTGTACGAGAGAAGCTGGTTCGGGTGCGGTGGCAAGCGCGGCGAGGTCGACGACGAGCGGGCGCCGGGCTGCGGTGTGCAGGGCCGCGATCGCGAGGCCGTGCGGGTCGCCGCCCCGGTCGAGCAGGTGCACCAGGCCGCTGCCCGCGCCGAGGACGGCCGCGACCCGGGGGACCTCGGGCCGCTCGTCCGGCTCCGGGGGGCGGGTGTCCTCCCGGACGATCCCGCGCAGTCGGCCGTCGATCCCGTCGTCGCCGAGGAGATATGCGGTGACCCGGTCGGGTACGCACAACAGCCGGGAGAGTAGCGGGCGTTCGGGCTCGGCGATCTCCAACAGGCCGCCCGCGACGAGCGGGGCTGCGGGCGCGAAACGGAAGCGGCCCGCGCCGGCGGCGGGCAGCCCGCACAACTCCAGGGCCAGGCCGATGGTGGGGCGGCGGCGGGTGAGGTCGTCGTTGAGGTAGCCGTACAGCCGCTCGAACCGGGGGTCGATGTCCGGGGCCAGGGCGACCAGCAGGAGGTCGACGTCCAGCGGTGCCAGACCGAAGCGTTCGGCCAGCTCGTCGAGCCGGCCGCCGTCTCCCGCACCGGTCGGCGCCCCGTCCCCGTACGCCGGTACGGGCGTGAACGCGTCGCGGCTCTCCAGGATGCGGGCCGCCGCCTCGGGGGTGAGGTACTGCCCCCGGTAGGGGTCGTCGGGGTCCGGGTCGACGGCGCGGCGGGCGGCGACGGCCTCCCGGACCCGCTGTTCGACGTGGCCGAGCCGCTCCCAGAGCACCTCGATGTCGGTCAACTCATGCTGCTGCGAAGCCTGTTCCACTGCCGGGGTCATCGTGCGGCGTTCCCCCGCCTGCGTCGGCCGGGCGGCAGTCGCCGTTCCCGGGGTGCGGCGAAGCCCTGGCCGCCGGGGTCGGTCGCCCCGTCGTAGCGCAGGCGGCGGCCGGGGTCGCCGGGGCCGCCGTCCAGGTGCGGTGCGGCCTGCATGACGAGGCCCTCGGTGACCGGCGGTCCGGCGGCGGTGCGTTCGCCGGCCAGCGGGGCGAGGACCCGGAGGTCGATGGCGGCCTTCAGCTCGCCGCCGAGCGCGGACCAGACGTCGGAGGCGGACGGGCCGCCGGCTCCGGGGCCCGCCGCTTCCAGCTCGACGGTCAGGCCGAGTTCGGCGAGGCTGCCGGTGTGCAGCCGGGCGGGCAGCGTGTCCGTACGGACGAGGGTGCGCAACACCTCGGAGAGGAGGCGGTGTTCGTCCTGCGGGCGGTTGGTCCAGGCGGTGACCAGATAGGTCAGCTCGAACCAGCGCGGCGGGGTCCGCCACCCGGTGATCACGCCCTCCTCGTCGTGTGTCTCGGCCGTGCCGGTCCGCCGCCGGGCCGCGTCCTCGCGGATGCCGTGCAGGAAGACGCTGATGGTCGGGGCGTTGCGGCGGGCCGACCAGTCCTTCGTCGGGGCGTCGAAGACCAGGTCGACGCCGCTGTCCTCCAGTCCGGCCTCGGCGAGCAACAGCCGCAGCCCTTCGTCGACTTCGTGGATCATCGGCGGATCACCTCGTCGGGCGGGGTGATGGTGCCGAGCACCACGAGGAAGTCCGTCTTCACGGGGCTGAACCCGGGGCCCTTCGCGGTGATGTCGCGCGGTCCGATCTCGTCCTTGGCCAGGATGAGGAGCTGGGCGATGAACGTGCCGTCGCCCAGCGGCCGGGTCGGGGCGGCCGCGGCGGTGATGCCGGGCTTCCAGCTGAGGGTGACGGGCGCGCCGGGCGGGAAGTCCTTGCCGCGCACGGAGGTGACGAAGCCGGGTTTGCCGACCTTGGGCACCGCGATGATCCGGGGTTGCAGAATGCGCAGCGGGATCCGGGAGACGTTGTCGCGGAGGTTGGCGTCGGTGCCGGTGGTGGTGAGCGACGCGGTGATCGTCGTACGGAGCGCCTTGTCGGGCGAGAGGACGACGCTGATGACCGTGGAGGCGCGGGGCGCGAGGTCCGGGATCGTGCAGGCGCCCGCGGCGCAGCCCGCCGGGAGCGGCCCGGCGGGGATGCCCCGGGGCAGTCCGAGATCCAGCCGGAGGCCGGTGGCCAGGGCGTTCCTGCCGTTGCGGACGGTGTACGTGACGACCACCTTGCCGCCGACGTAGCCGGGGCTGGGCTGGGCCCGCACGGTGACGGCGGGCCCGGCCTCGGGCGCGGGCGGCGGGGGTGCGGGGGCCGGCGGCGGGGGCGGTGTGGTCGTGGGCGGCGGGGTGGGTGCGGGGGTCGTCGGTGTGGGGGTCGGGGACGGCGGAGGCGCCGTCGGGGGCGGGGTGGGCGGCGGGGCGTCCTCGACCGGGACGATCGTGCCGGTGGCGTTGTCCGTGGGGTTGGGATCGATGACGGTGCCGGTGACGGACCAGTTGACGCGCTGGATTCCGGTGGTGACGCCGGTCAGCCGGGCGGTGATCTCCACGTCGGTGCCGGGCGGGACGGTGCCGAGGTCGCACTGGGGGGTGCCGGGTGCGCAGGTCGCGGTGTCGGTGGTCAGCTCCTCCAGCCGTACGCCGGGCGGGGCGTCGACGGTGAGGGTGGTGCCGGGCGAGGGGGCGGGGCCCCGGTTGGTGACGGTGATGGTCACCTCGGTTTCGGAGCCGACCTCCACGGCGGGCCGGTTGGGCGGCGCGGTGAGCGACAGGTCGACGGACTGCTGGAGGGCGGGCTCCTTCTGCCGTCCGGCGTGCGCGTTGTCGACGGGGGTGAGCTCGCCGGAGGCGAGGTCGAGGACGGAGAGCTGCTCCATGGAGTTCGGGGCGAGTTCGCGGCGCGCGCTGAACACCAGCCGGTCGCCGCCGGGGGTCCAGGCCACGTCGCGGGGCTGGTGGGGGCCGGTCGCGGAGGTGTCGGGGATCGGCAGGTCGCAGCCGGCCGGGTTGTCCTTCTGGACGGAGGGCAGCACGACCCGGCAGCCGCCGCCGCTCAGGGGCTTGACGATGACGCCGGCCTGCTGGTTGACCCTGCCGCCGCCGTCCTTGCGGTTGAAGGCGACCTTCAGGCCGTCGGGGGAGAACGCGGGGCTGTCGTCGATGACGTCGCAGGCGCCGGGGCAGATGGTGGCGCTGAGGTCGCGCTGGTTGCCGAGGTCGGCGACCGGGACGACCCAGATGTGCTTGTTGCCGCCGTTGCCGTTGATGACGTGGTTACGGGTGAAGGCGAGGTTGTCGCCGTCCAGGGACCAGGTCGGCTGGGCGTCGCCGCCGGTCTGCTGACCCGCGGGCGGCCGGATCTCGTCGAGGATCTCACCGCTGGCGACATCGGCGACGAGGATGCGGCTCGGGCCCGCCGCGTCGCCGGTGCCGCCGGGCGAGGTGCGGGTGAAGGCGAGCCTGGTGCCGTCGGGCGAGAAGGCGGGGTCGGTGTCCCAGTCGTTCGGGCCGCGCCCGGCGAGCGGCAGCGCCGCCGCGTTCCCCCCGTCGGCGTCCGCCATCCAGATCCGCTCGACGCGCCCGGCGTCGGTGTCCTCGAAGCGGGTGACGACGATGCGGCGGCCGTCGGGGGTGTAGCTCTGCCGCTCGGTCCACGGGTCGAAGCCCGGGCGCGGGTTGAACAGGCGGTCCACGGCGGCGTCCTGGTTGGTGCGTGCCTCCGGGTCCTCCTTGAGGATCGTGAGCCCCAGGTCGCGGGGGTCGGAGCCGTCCTGGCGCACGTCCTGGAGCGTCACGACCTGCGCGGCGGACAGCACTTCGTCCTCCTGCTTGACGGTCTCCGGGTCCGGGGTGATCCGGGGGACGACGACCGTCCCGGCCGGAGGGAACCAGGTGGGCGGCCCCACCTCACGGTTCTCGTCGACCAGTTGCTCCGGCTCCTTCGCGCCGTCGAAGGCGGTCACCCGGTAGACGTGGTCGAAGTCGTCGCAGCCGCAGGTGTGGTACGGGCTGAGGAAGACGACGTCCTTGCCGTCGGGCAGCCAGGAGGCCGAGCGGGTGCCCCATTCGGCGTGCCCGCCGGCCAGCAGTGGGCGGTCGGTGCCGAGCCCTTCGGTGGCGCGCAGTTCGGTGCCGTCGTCGACGTTCGGGTCGGGGTTGGTGGTGAGGGTGTAGGCGACGATGTTCCGGACGGCGGGGTCGGCGCCCGGGTTCCAGGACGGCTCGGTGGCGTCACCGGCCCCGGCGTCGCTGATCCGGGTCTGCGGGCCGCCCGCGACGTCCCGCACGTAGATCTGCCAGCCGAGGGCGGTGTCGCCGTCGCAGGCGTACGCGATCCGCGTGCCGTCCGGGGACCAGGTCGGGGACTCCTCGTTGTCTGCGGTGTCGGTGAGCCGCCGCAGGTTCGAGCCGTCGACGCCGACCGACCAGAGGTCGCGTTGGACCGTGCCGCCGGGTCCTGGCTCCGCCGAGTCGAAGACGACGGTCCGTCCGTCGGGGGAGAGTTCGGGGCGGGCCGCGTCCCGGCCTTCGGTGAGCCGGCGCACCGACCCGTCCGCGCCGCGCAGGTACACCTGGGGCTTGGCGCTGTCCCGCAGGCTGGTGAAGACCAGGACGTCACCGCGGGCGGAGGGGTCCTGGTCGTAGTGGGCGGGCCCGTCGCCGAACAGCGGGTCGGTGCGGTCCTGGTCGTTGGCCCGCCCGAGGCTGCGGTGGTCGGTACCGGCGAAGGCGATCCGCCCCGCCTGGGCCGGGTCTGCGTCTGCCGGGGCGGCGACGGCCTGGCCCGCCCCGTCCGGGGCGGCGGCCGAACCGACCAGCAGCAGCGGCGCCAACAGCACCACCGCCCCGGTCAGTCGGCCCAGCCGGGAATGCTTCGCCGGGCCAGCAGTGCCGGTCACGGCCCACCTCACAGTCTGTCGATCGACTCTCCACCGGCCAGCCTCGCGCCCGCGTGGGGGTGGGGAACAGGCCGCGAGTACCCGGACCGGGGGAAGGGACCGCTGCCCTTTGCGGCGGTCGCCCCTCCGTCAGATCAGCCCGTGGCGCATCGCGTAGCCCACCGCGTGGGCCCGGTTGCGCAGTTCGAGGCGGGTCGCGACCTCGTGCAGCACGTTCTTGACGGTGCGTTCCGAGTACGAGGTCTTCTGCGCAATCTCCGCGGTGTCGCAGCCCTCCGAGACCAGCCGGATCATCTCCGCCTCGCGCGCGGTGAGGGTGGACAGGGTGAGCCCCCGGGGGTCGAGGACCGTGCGCTGGAGGGAGCTGACGTGGTCGAGGAGCTTGCCGAGCAGATCGCCCGGCAGGACGCCCTCGCCGTTGGCCATGGCGCGCACCAGGTGGACGAGCCGGTCCTGGTCGGCCTCGCCGCGCCGGAGGACGGCGGCGACCCCGCACTCGATCATCGTCTGGAGGGCGCCCGACTCGAAGTACCCGACGACCAGTCCGGTGCGGGTGGAGGTGTTGCGCTGGAGGCGGTGGAGGAGCTGGACCGTGGTCTCGCCCACCGTGTCCACCACGACCAGGGAGACCTGCGCCCGGTCCGCCTCGGCCTCCGGCAGCAGTTCTATCTCGGGGCGCACGCGCAGTTGGTGGATCATGCCGGTCTGCAGGATCAGGTCCTCCGCGTACACCGCGACGGAGACCCTGCCTCCGGGCGCTCCCCCGGCACCGGTGGTCCGGCGGCCGGCGGCGTCGGGCCTGCGGTACTGCCCGCGTGCCGCCGTGCTGTTCGTCGTTTCCGTGATCGTCATCGTTCGTGCCCGTCTTCCTCAGGTACTTCAGCCCGATATGCCTGCTGTTCTCGTGATCGCCCGCGCCGGCCAGGGCAGGGCGACCGGGCCCGGCGCGGGGGCGCGGGGACACCGTGCCGGTGGGCCCGCGGGGCACCACCGCTGCCCGCTTCTTGCCCTTGCGTCTCTGCTGCCGCGCGGTACCGGCGGCCTACCGTCGCAGAGTGACCACATCTGCCGAACTCGCAAGCCCCACGGTGACGGTGTCGCCGGGCGGTACCGCGACGACCACCCTGACCGTGCGCAACGACGGCGACATCGTCGAGGCCTACACCCTCGAAGTGGTCGGCGACTGTGCCGCCTGGACCACCGCCGAGCCGGCGCGTGTGTCGCTGTACCCGGGCACCTCCGAGACGGTGACCCTCACCTTCGCCCCGCCCCGCTCCCACGAGGTCCGGGCGGGCGAAACCCCCCTGGCCGTACGGGTGCTGCCCGCCGAGCGCCCCGAGTCGGTGGTGGTCCCGGAGTCGACGGTGACCGTGGAGCCCTTCCACGAGCTGCGCGCGGAGCTGGAACCGCGCCGCCGCCGGGGCTGGCTGGGTGCCCGGTTCCGTACCGCCGTGCAGAACAAGGGGAACACTCCGGTCGACGTGGCCCTGGCGGGCCGGCAGGACGGGGAGGATCTGCGTCTCGCCTTCACCCCGGACAAGAAGCGGCTGGAGCCGGGCGAGTCGGCGGAGGTCGCGCTGAAGGTCCGGGCCCGGAAGCTGATCTGGTTCGGCGAGCCCGTCGCCTGGCCGTTCGAGGTCCTGGCGACCGAGGGCGGCGAGGGGGACGCCGAGGCCGGGACGGCCGCCGAGGCCGCACAGCCGGGTGAAGCCGAGCCGCTGCCCGGGGAGTTCGCGCAGATACCCGTGCTGCCCAAGTGGCTGCTGATCGTGCTGGCGGCGCTGCTGGCTCTGCTGCTCGCCTGGTTCGCCCTGGTGCGTCCCGCGGTGCAGAGCACGGCCAAGCAGGCCGGGGCGAAGGCCGCGCAGGAGGAGACCGAGCGGGGCAAGGAGCAGGGGTCGACGCCACCCGGCGGTGCGGAGAACCCGGCAGGCGGCCAGGGCCAGGGAACCGGTCCGGACGGCACGGGCCCCGGCGGGACCGGTTCCGGACCGGGCTCCACCGGCGGGGGCGGCTCCACGGGCGGGAGCGGTGGCAGCGGGGGCGAACAGGCCTCCAGGACCATCGACGTGCAGACCCGGGCAGGGGCCGAAGGGGAAGGCACCTACAAGGTTCCGGCCGGGAAGGTCTTCCGCGTCACGGACGTCGTGGTGGCGAACTTCCAGGGCGACGAGGGCCTCGTGACGATCTCCTTCGGCGAGAACAAGATCACGACGATCGCTCTGGAAACCTTCCGCAACCAGGACTATCACTGGGTCACCCCCATTCAGGTTCCGGAGAACGCCACCGTCACCGCTTCCGTCACCTGTGCCAAGCCCGGCACTCCGGCAACCGGAACACAGGCTTCCGGGTGCCATCAGGTTCTGAATGTCAGCGGTGTACTGAGCGATCTCGCTCGATAGAAGGACGATAGAGGGACGATGGAACGAGGTGAGGAGCACGGCGGAAGCAGCGGCTCCGAACCCTCCGCCGCGCCTGTTGACGAGACAACAACAGAAACCCGGCCGGGAGGAAACCCAGCCTGCCGGGCGATGGCGGATTCACCCTCCCCACCGCACCGGAGATCTCCGCCGGTTCGGTCGTCCGCGACGTCGGCAGCACCGGAAGAATATCCGCTGCCGGCGGCCGCAGACACGAACGGGCCTGCTCAGAGGTGGTTCTGACGGTTTGGTGAAGGTCGGCCGATGCCCGTTCGGAGCGCTTTCGCGCCCGTTTCCCTCATGCGCACCGGACCGAATCCGCCAGCCATCCCGACTCATTCTGGCTGAATCGCATCACCACCACATCACCGTCGCATCACCTCGGAGCGTTTCCCCCGCACCCCCGGACGGCTATGGGCCATCTGCGGTTTACCGAGAAAAAGAGATACCAAACACATGGGGTCCCCGGCGCGCCGCCCACCCATTCCCTTGAACCCCGTTCCGGTGCGGCCGCGTTGATCCCTTCCGTGACACAGTGTTCTCGTTCTCTTCACGCAGTCGGTGGAATGCGCGTCGGGAACCGGGAATAGGGCGGATGGCTCCGGCCGGGCCGCCGAGGGCAGGGTTACCCGGCGTTCGAGAGTCCGGAAAGGGCAGCCTCCTTGCCCCGGGTCCAGGACTCCGGGACCTACTCCCGGCCCGTACGGCCGGTCAAGACTGGGCGGTGATCGAGTGACCGTCCAGAAGGAGCGAGCATGCCGTCGTACCTCACCCCCGGTGTTTACGTGGAGGAGGTGCAGTCCGGAGCACGGCCCATCGAAGGAGTCGGCACCGCGGTCGCAGCCTTCGTCGGCTTCGCGGGGACGGGCCCCTTCCACCGGCCGACGCTGGTGACGAACTGGGACCAGTACGTGCAGACGTTCGGCGCCTTCACCGCCGACACCTACCTGGCGCACGCCGTCTACGGCTTCTTCGCCAACGGCGGCGGCGCGGCCTACGTCGTGCGCATCGGAGGCCCCGCGGAGGGCGCCGACACCACCGGCCAGGGTTCCGTCGCCCAGGCCCCCGCACCCGTCGCGCTCGGCGGGTTCCTGGTCGCCGCCAAGCCCGGCACGGGCGACGGCCTCTCCGTGGAGATCGCCGACGCCGAGGGCGAGAACCCGCCGGAGGACCGCTTCCGGCTGCTGGTGCGCCAGGGCGGCAAGGCCGTGGAGACGTACGACGTCTCCACCCGCAAGAACGTCAAGGGCTACCTGGTCACCCAGGCCCGCGACTCCAAGCTGATCCAGGTCACCGAGCAGCCCGGCACGGCGCAGAGCCGCCCCGAGAAGCAGACCGTGGCCCTCGCCCCCGCGACGGCGGCGGCGCCCGGCAACGGGGTGGCCCGGCTCGACGCCTCCGAGTACGTGGGCGACGCCTCCGCCCGTACCGGGTTCGCCGGTCTCGAAGCGATCGACGAGATCACGATGGTCGCCGTCCCGGACCTGATGAGCGCCTTCCAGCGTGGCGACATCGACGCCGAGGGCGTCAAGACCGTGCAGCTCGCGGTCATCTCGCACTGCGAGCAGATGGGCGACCGCGTCGCCGTCCTCGACACCCCGCCCGGCATGAACGCCCAGCGCGTCCGCACGTGGCGCAACGAGGACGCCGGCTACGACTCCCGCTACGCCGCCCTCTACTACCCGTGGGTCAAGGTCTTCGACCCGGCGAGCGGCCGCAACTCCCTGGTTCCGCCGAGCGGTCACGTGGCCGGCGTCTGGGCGCGCAGCGACAACGAGCGCGGAGTCCACAAGGCCCCCGCCAACGAGGTCATCCGAGGAGCGGTGGACCTGGAGATCCGGCTCTCCAAGGGCGAGCAAGACCTCCTCAACCCGATCGGCGTCAACTGTGTGCGCGCCTTCCCCGGCCGCGGCATCCGCATCTGGGGCGCGCGCACCCTCTCCTCCGACCCGGCCTGGCGCTACCTCAACGTCCGCCGCCTCTTCAACTACCTGGAGGAGTCCATCCTCCTGGGCACCCAGTGGGTGGTGTTCGAGCCGAACGACGACCGCCTCTGGTCGAGCATCCGGCGCAACGTCACCGCGTTCCTCACCGAGGAGTGGCGGCGCGGCGCGCTGTTCGGCCGCACCGCCGAGGAGGCGTTCTACGTGCGCTGCGACCGGAGCAACAACCCGCAGGAGTCGATCGACCTCGGTCAGGTCGTCTGCGAGATCGGGGTGGCGCCGGTGAAGCCCGCGGAGTTCGTGATCTTCCGGCTCTCGCAGTTCTCGGACAGCACCAGCCTCGTCGACGAGTGACCTTCGCGGTCCTCCCCCACCCCTTCACTTCCCGTCCCGATCAGAACAGGTGACACACAGTCATGGCAGAGGGCGACGCTCTTTCCACCCACGTCTTCGGCGTTCAGCTCGGCGGCTATCTCGTGGAGTCCATCCAGGAGATCAGCGGCATGACCGTCGAGGAAGAAGTCGTCGAGGTCCGTCAGGTGACCGCCGACGGCAAGCAGATCATCCGCAAGCAGCCGGGCGCCCGCCAGGCGGGCGAGGTGACGATCACCCGCGGGCTCGACAAGAGCAGCGAGTTCACCACCTGGATCAAGGAGACCCTCAACAACGGGGCCGTCGACACCGCCCGGCAGAACCTCACGATCGAGATCAAGGACTCGACCGGTGAGACCGTCCGCCGTATCCAGCTGATGCAGGGCTGGGCCTCCAAGTGGGAAGGTCCCTCGCTCAAGGCCGGCGAGTCCAGCGCGGCGACCGAGACGGTGACCATCACCTTCGAGGAGATCGTGGTCGAATGAGGCGCCGGACCGTTACGCCGGGGGCCGGGCTCGAAGAGACCCTCGACAACCTGGCCGCCGCGACCGCCACCCGCCAGGAGGCCCCGGCCGCGGCGGCGCCCGCCCGCGCACCCCGGCGCGAACGGGACACGCTGCAGACGGAGTTCGCCTTCGAGCTGCCGCGCGGGTACGTCGACGACGAGGGACAGGTGCACCGGAACGGCACCATGCGGCTCGCGACGGCCCGGGACGAGCTGAAGCCCCAGATCGACCTGCGGGTGAAGGAGAACCCGGCGTACCTCTCGGTGGTGCTGCTGGCCCAGGTGATCACCCAGCTCGGTCCGGTCACCGACGTCCACACGGGGATCGTCGAGCGGATGTACGCGACCGACGTGGCGTTCCTCCAGGACTTCTACCGCCGCATCAACAGCGAGGGGCACACGCATGCCGCGGTGACCTGCCCGCTGTGCCACGGCTCGTTCGAGGTGGACCTCTCGGGTGGGCGCCTGGGGGAATCGTGACGTACGCGCTTCCCCGGCTGCGGGAGGAGATCGCGTACGTCGCCTACCACTTCCATTGGCAGCGTGAGGACATTCTCGACCTCACCCACGGCGAACGTCAGCAGTGGGTGCGGGAGATAGCGCGGATCAACACCCGCGTCAACGAAGGCGGGTGATCCTGTGGGGTTCGGGGACTGGCTGCGCCGGACGGACCGTCGGCGGTCCGTGACGCCGTCGCAGGAGAGCGAGGCGCGGGGCGGGGGCGGGCGCGACGACGTGTCCACCGTGCCGGCAGTGCCTGCCGGGGCCGGTGGCGGCAACGGTGATGCCAACGACGGTGGCTGGGACGGCGGATGGCGGCGGGTGGCCCCGCCGTCGGTTACCGTCGCCCGGTCCTCGATCGGGGTGAGCGACGGGCTGCGGTTCCGCTCGCGCCTGGCCTCCTGGCAGAACCCGTCCCTCGGCGGCGAACTCGGCCATGCCGTCCTGCCGTCGGCCCCGGTCGGCCTCATCCACGGAGTCGCCCGCCCGGGCTCGGCGCGGCCCTCGGCGTCGCCCGGCGGCCCGCTGCTGCTCCGTGCGGTCCGGCCCGCCGACGCCGAGGAACCCGCCGAGCCCCTCGGGCCCGCATCGGACCTGCCGTCCGGCCCGGCGGGGAGGGCGTCCGCACGCGGTACGGGTACGGGGAAGCCGGGTCCGGCGTCGCCGCCGGTCCAGCGGTCGGCGGCTTCCGGCGCCAACCGGTCCTCGCCTGGTGCGGCGAGGACCACGAGCCGGCCGTCGTCGCGCGCTTCGGAGCCTGCGGACCGGTCGTCGGCCGACGCTTCCGGGACCAGGTCGGGGGCGTCGGGTGCCCCGAGGCCCGGGGACCAAGGGTCCGGGAACCGGCCGTCGTCGGGTGCCTCCGGACCTGCGAACCGGTCGTCATCAGCGGGTACGCCGGGGACGGTGTACGTGTCGCGCTCGGCAGCTTCGACGGGACGTACGGCCGCGTCGGGTACGGCGGGACCCGCCGACTCGGCCCGGTCCGGGGAGGCGTCCAGGGGCGCCTCCGGGAGCTCGAACACGGCGCGGTCCGGGCCGGCGACCCCTTCTGCGGCCGGATCGGCGACCTCGTCCAACTCCTCGCTCCGGTCCGGCTCGTCGGGCTCGTCCCGCTCGTCGGACTCGGTCGGCTCGGGCGCCTCATCGGGTTCGTCGGAGTCGGTCGGCTCGTCCGGCTCCGTCCGCTCGGTCGGCTCGTCCGGCCCATCGGGCTCGGTCGGCTCGGCCGCGCGTGCGGGGGCCCTTCCCGCTCCCGGACGGCCCACGCTCGGCCCCGGCAACAACGCTGAGGCCGCCGCCCGCCCGCCGACGCGGCCCGTTGCCGTGCGCCCGGAGCGGATCGCGCCGCCGCTGACCGTGGCCCGGCGACCGGCCATGCCACTGCGGCAGATCACCGCGCTCGCGCCTGCCGCACCTTCCGCCCCCGCCCCCACCCCCTTCTCGGCGGCGTCTTCGACAGCCGCACCGGCGACCGTCCAGCGAGCCGCGTCCGAGCGGGGGAGCGGCCCGGACCGTACGGGGTCGGTCACCCCGGACCGTACGGGGTCGATCGCCCCGGAGCGTCCCGCTCCCCCGACCTCCGGCCCCGCCTCCACCCCCGACCGGCCCGCCCCCGAGGCGGTACGCCCGGCCCTCGGCAAGCCGCTGCGCGAGATGCCCGCCGGGGCCAGGCCGGCCGGTACCGACGGACCGGCGGGCGTCGTCCCGTCCGCTCCCGGGGCCGTGCCTCCGGCAGCAGCGGCCATGCCGGTGCTGCAACGCCAGACGTCGGAGCCGCCGAACCCGCCAAGTCCTACGAGTCCCCCTCCGGCCGCAGCGCCCACGGCCCCCGCGAAGCCCTCGCCCACGCCCTCGCCCACGCCCTCGTCCTCCAGTCCGGCCGAGGCCCCGGCACGGCGTCAGCCGTCGTCGAACCCGTCCGAGCCCTCCCCCTCGGTGCAGCGCGCACCGGCCCCGGGGCCGAACACGTCCGCCCGGGTGCGCGGGGGGATCGGGGCACCGCTTCCCTCGCTGCCGCCGACCGCCCGGCTCGACGGCGGCGCTCCGCTGCTCGGTGACCGTCCGTCCACCGTCACGCACCCGAACACGGACCGGGCTCCGGGTTCCGGACCGGCGGCAACTCCCGGCTCCGGGGCCACGGTTCCGGCCCCCGCCGCGACACCACCGAGCGAGCCCGCCGCGATGCCCGTGAGGTCGGCACCCGCCGTCACCAGCGGCCCCGCCGAACCGTCCGGGCCCGCACCCGCACCCGCACCCGTCCAGCGCTCGGCCGTCACCACCACTCCCCCGCCCCCGGTGCGTATCCGGCCCGTCCCCCGGGACCGTACGGCCGCGGCACACGGCTCCGCCGGTACAGCACCCCCGTCCACATCCACATCCACTTCCGCGTCCATGTCCACGCCCGCCCCCGGGGGCCGGCGGGCACGCACCCTGCTCCCGGACCGCCCCCTGAGCATCAACACCGGTTCCGGTGAAGGGTTCTCGGGGCCCCCGGTGGCGACGGGCGGCGGCTCGTCCCGCCCGGTCGTCGCGGCCACCTGGCGGCGCGACGCGGCCCAGCCCGGGCCTGCCGCCGCACACACCAGTGGCGGGCCGGGCGCCGGTTCCCGGCAACCGGCGCCCTCCGGGGCGATACCGGGCGCCACGGTCCAGCGCTCCGCGACGACCGACGCCCGGCGCGGGCCGTCCGCCGGTGGCGTGCTGCAGCGACTCGTCCCACGCTCCGGGCAGGCCGCGACACCCTCGCCCGTGCCTCCCGTCGCCCAGCCGCCGCATCAGGCGTCCGGACCGGCGACCCGCCAGGCCCCGGAACCGGGCCCCGCGCGGCGGCCCCCCGTGGTCCGGCCCCGACCGCCCGCGCCCCGGCCGGCGGACGCCGCCCCCGTACCCGTACAGCGGCAGGCGATGCCGGTCGTGCCCGACGGTGCCGGTCCGCCGGCCGCCGGACCGGCCCCCGTGGGCGGTGCCGCTCCCGGCGGGCCCCCGAGCCCTTCCGTGCGGGTGCCACCCCGCCCGGCCGCGCAGGGTGCCGGACCGGGTCGCCCGGAGACCCGGGCCCAGGCGGTCCAGCGTGCGGCGGCGAACGCCGGGATCACCGGGGTGCCCGTCCAGGCCGCACCGGCGAAGCCCGCCGCCGGGGCGACGGGGGCGGCCACCGGCCCCGTCGACGCTTCCGACGCCTCCTCCCCGGCAAACCGGCTGAGCGGAACGGAGATCGAGGAGCTGGCCCGGCGGCTCCTCGATCCGGTGAGCCGGCTCATCCGCGCCGATCTGCGCCGGGGCCGGGAGCGCAGTGGGCGGCTGCACGACGGCCGCCGCTGACGGCACAGGCGCCAGCACCCGCACCCGCACCCGCACCCGCACCCGCCACACCCGTACGACCGACCGCAGAGAAGACGAGAGACGCATGACCGACAACATCTTCGCGACGAGCGTGTTCTTCAAGCTCGCGATCGGCGGCAGCGACCTGGGCGCGTTCCACACCTGCTCGGGCCTGGGCGCCGAGGTGGAGATGGAGACGTACGCCGAGGGCGGCAACAACGGCTTCACCTGGCAGCTGCCGGGGCGGATCACCTGGACGAACATCACGCTCACCCGCCCGGTGACCACCGACACCCTCAAGATCGCGCGCTGGCTGAACGAGACGATCCAGCGGGTCGAACCCAAGGACGGCGAGATCGTGGCGCTGCGCCCCGACCTCAGCCGGATCATCAGCTGGCAGGTCCACGGCATCGTGCCGGTCCGGTGGCAGGGGCCGTCCTTTGATCCGGCCAACTCCGAGGCGGCGATCGAGACGTTGGAGATCGCGCACGAGGGCCTGGAGCCCTCCTGACCGCCGACACCACATCCAGCAGGACCAGGACGCAGAAAGGAGGAACGCAATGTCACCCGCTCTCCGCGCGAGCCGCGCCCGTGCCCAACTGACCGTCATGGAGCCGCCGTCCGCCGTCGGCGCCAAGCCCGGCGGCACGCTCGCCCGTCTCACGTTGCAGTTCAACCCCGCCAAGCTGTCGCTCAGCAAGAGCACCGAGTGGCGGCGCACCCCGTCCCGGATGGCCGGGCAGTCCGCGCTGCCCGAGTTCGTCGGCAGCGGTCCCCGCGCCCTGTCGCTGGAGGTGTTCCTCGACGCGACCGCCACCCACGACAACTCCGTGGAGAAGGCGGTGGAGCAGTTGATGACCGCCTGTGTCCCCACCCCCAGCAGTCTGGCCCGCAAGACGCCCGCCAGCCCCTGGGTGCGGTTCGACTGGGGGACGTCGAAGACGACCTCGTTCGACGGGGTGCTCTCCAACCTCTCGGTCTCCTACACCCTGTTCGACGTCGACGGCAAGCCGCTGCGCGCCACCTGCTCCCTCTCCATCGAGGAGGCGAGCGTCGACCCGGCGGGCCAGAACCCCACCTCCGGTTCGAAGGAGGCGCGGCGCACGCACCGGGTGGTCGCCGGGGACAGCCTGCCGCTGCTGGCCTGGCGGGAGTACGGCGACGCCACCGCGTGGCGCACCATCGCGCACGCCAACGACATCGACGACCCGATGCGGCTGACGCCCGGCCAGGAGCTCCTGGTGCCCGGTCGCGAGGACCATCCGGCGGAGGGCGGCCGATGAGCGGGAAGGACTCCCCGGGCCGCTCGTTCGCCGCCGACCCGATCGTCGAGGCGCCCGCCGAGCTGCCCGCCGCCTGGGCCACCCAGCTGGTGAGCTGTGTGGTCGACGAGAACGTGGGCCTGCCGGACACCGCCGTCCTGATGTACCGGGACCCCGACCACACCTTCCTCTCCAGGACCGGTATCGGTATGGGGACCCCGCTGAAGATCTCGGTGGTCACCGTGAAGGACCGGGCGCGCGAGCGGCTGTTCACCGGGGAGGTCACGGCGGTCGAGCTGGACACCGACACGACCGGGTCGTTCACCGTCGTCCGGGCGTTCTCCAAGGCGCACCGGCTCCAGCGCGGCAGGAAGGTGATGGCGTACCGGAACATGAAGACGGCGGACATCGTCCGCAAGGTCGCCGCCGGGGCGGGTTTGGCGGTCGGGCGGATCGAAGCCGCGCCGGTCACGTACAAGCAGCTGACCCAGCCGAACGTCTCGGACTGGGAGTTCCTCCAGCACCTCGCGGCCGAGAGCGGGGCCACCGTACGGGTCGACGACAAGGGCCTGTTGCAGTTCACCAAGCCGGACCCGGCGTCCTCGGCGCCCTCGCCGTCGACGTCCGCCACGCGCGACCCGATGGTCTTGGAGTACGGGAACAACCTGCTGGCCCTGCGCGCGGTGCTGACCGGGGCCGACGGGTCGGACAGCGTGGAGGTGCGCGGCTGGAACGTCGACACCAAGACCCGGCTGGTGGCCCGCCAGCAGTCCGTGCGCAGCGACACCGTCGCCCCGGGGATGAGCCCGTCGGACGCGGCGCGGATCTTCGGTTCCGGCGGCTCCCGCACGACGATCGCCGACACCCCGTACCGCACCCAGGCGGAGACCCGGGCCGTCGCCGGGGCGCTCGCCGCGTCCGTCAGCGCCGGGTTCGGCGAGGTCGAGGCGGTGGCGTACGGAAATCCGCAGCTGCGGGCGGGCCTGCCGGTGGCGCTCGGCAACGTGGGGCCCGCGTTCTCCGGCCGCTACACCGCCACCGCCGCGCACCACGTCCTGGAACCGGACACCGGCTACCGCACGACGGTGATCGTCAGCGCCTCGCCGGACCGGTCGCTCTCGGGGCTGACCGCCGGTGCGAACGCCCCCTCGCGCGGTCCGCGCATGCCGGGTCTGGCGATCGGGGTGGTCACCGACATCCGCGAGGAGGGCAAGGGCCAACGCGGCTGGGTGCGGCTGAAGTTCCCCTGGCTCGACGACACCTACGTCACCGACTGGGTCCGCACCGTGCAGTGGGGCGGCCAGGGCGGCGGCGGGGTGTTCAGCCCCGAGGTCAACGACGAGGTGCTCGTCGGGTTCGAACAGGGGCTGCTGGACAGTCCGTACGTGCTCGGCGGGCTCTACAACGGAGTCGACAAGCCCTCCCCGCACGACGTCCCGCTCGTCGACCCGACCAGCGGGAAGGTCAACCGCCGTTCCCTGGTGTCCCGTTCGGGGAACCGGCTGGAGCTGCTCGACGCCCCGCGCGGTCCGGCGGGCGTGCGCATCGCCACCGGCGACAAACGGCTCGATGTGGTCCTCGACGAGAAGAAGGGCGAGATCACGCTGACCGTCAAAGCCCGTGGCGGTGGAAGGGAGTTGAGCTCCGTGACGCTGTCCGCCTCGGGCATCACGCTGGACGCGGGAGCCACCGGTGACGTGAACATCAAGGGCCGCTCGGTGACCGTCAACGGCAAGACGGGGGTCACGGTCGACGGCGGACTGCTCGCCGTCCTCAAGGCCAAGCTCATCAGGATCAACTGACCGCCCGCCCGCTTCCCCCTCCCCGAAGTCCCTTTCACAGCAAGGAGAACCCCGGCCATGCCCCCCGCAGCCCGCACGGGCGACAGCACCGCCCACGGCGGTCTCATCGGTACCCCGCCCCCGGGCGCGTTGGCCGTGGCCACCGTACTCATCGGCGGCCGGCCCGCGGCCGTCACCGGGAGCCTGCACGGGTGCGTCGTCCCCCCGCACGCGGCGCTCGGCCCCGGCAACGTGATCATGCCCAACCCGGCCGCAGCGATCGGCGGCGCGGTGCTGATCGGCGGGCTGCCCGCCGCCCGGATGGGCGACAAGACCACCTGCGGTGCCCCCATCGTCAGCGGTGCGTTCAACGTCCTGATCGGGAGCCCGATGTGAGCGGCGACGGATACGCCGGACGCGGCGGCGGATTCATCGGGCGCGGCTGGGGCTTCCCGCTGCGGACCGGGCCGACGGGCGGCATCGCCCTGGTCGAACGGGACAAGGAGATCGAGGAGGCGATCGGGCTGATCCTGGGCACCGCGCCGGGCGAGCGGCCGATGCGCCCCGAGTTCGGCTGCGGCATCCACGAGTACGTCTTCGCGCCCGGGGACGGGGCGACCGCCGGGCGGATCGCGCACGAGGTCCGCACCTCGCTGGAGCGGTGGGAGCCGCGGATCGAGGTGACGGATGTGGTGGTCGCCTTCGACGCGGTCGAGGAGGGCACGCTCTACATCGACGTGCACTACACCGTTCGGGCCACCAACGACCTGCGCAACCTGGTCTTCCCCTTCTACACGATTCCCTCGTCCGAGGGCTCGGCCGCGCGGTCCGCCCCGGAAGCGGGGAGGCTCTGATGGCTCTGCCCTCCCCCAACCTGGACGACCGGCGCTTCCAGCAACTCGTCGACGAGGCCAAGCGGTTCGTCCAGCAGCGCTCCCCCGAGTGGACCGACCACAATGTGTCGGACCCCGGGGTCACGCTCATCGAGACGTTCGCGTACATGGTCGACCAGTTGCTGTACCGGCTGAACCGGGTGCCCGACAAGAACTACGCGGCCTTCCTCGATCTGCTCGGCGTGACACTGTTCCCGCCGACCGTGGCGCGGGCCGACATCGACTTCTGGCTCTCCGCACCGCAGCCGGAGACCGTGCACCTGCCCGCCGGTACGGAGGTGGCGACCGCGCGCGGTGAGGCCGAGGAGCCGGTGGTGTTCTCCACCTCCGAGGACCTGCCGATCGTGCCGAGTTCGCTGGAACGGCTGGTGACCGCGCCGGTGTCGGGCGAGCAGACGGACCGGACGGCGCCGCTGGGCGCGGGCAAGGACATCCCGTGCTTCCAGGCCCGGCCGGAGCCCGGCGACGCCCTGCTGTTCGGGCTGCCGACGGCGGTGCCCCGGTGCATCGTCGCCGTCCGGCTGGACAGCCGGGTGGAGGGCGTGGGCGTGGATCCGCGGCAGCCTCCGCTGGTGTGGGAGGCGTGGGACGGGGCCCGCTGGGTGGTCTGTGCGACCGGCACCGACTCCACGGGCGGCCTCAACCGGCCCGGTGAGGTGGTGGTGTTCGTCCCGGCCGGGCACACGGCATCGGTCGTGGCGGGGACCCGGGCGGGGTGGCTGCGCTGCCGGGTGACCGCCCCGGAGCCGGGCCAGCCGTTCTACTCGGAGTCGCCGACGATCCGGGAGGCCGAGGTGTTCACGGTCGGCGGCACGACGGCGGCCGAGCACGCGGAGACCGTCCTCGACGTGCCTCTCGGGGTGTCGGAGGGCGTCGCCGGGCAGCGGTTCCTGGTGAGCCGGGCGCCGCTGCTGCTGGACGGGGACCCGCCGGTCGTCCAGGTGTCGACGGACGAGGGCTGGGAGATCTGGACCCCGGTCGAGCACTTCGGCGCGTCCGGCCCCGGGGACCGGCACGTCCGGGTCGACGCGGTCGCCGGGGAGTTCGCGTTCCCGCCGGAGGTGCGGGAGCCGGACGGCACGATGCGCGCGTACGGGGCGGTGCCCGCGAAGGGCGCCCAGCTCCGCGTCCCCCGCTACCGCACGGGCGGCGGATCGGCCGGGAACGTCGCCCGGGGCGCGATCTCCGTGCTGCGCAGTTCCGTGCCGTACGTCGCGGGCGTGAACAACCGCGAGGCGGCGACCGGCGGGGTCGACGGGGAGACCGTCGAGAACGCGAAGGTGCGCGCCCCCACCATCCTGCGGGTGCAGGAGCGGGCGGTCACCGCCGAGGACTACGAGCTGATCGCCCGGGAGGCCGCGCCGTCCCTGCGCCGCGTGCGGTGCCTGCCCGCGGTGCCGGGCGAGGCCGGTGCGGTACGGGTGCTGGTGGTGCCGGACGCGGTGGCCGACGAGGACGGGCAGGTGCGGTTCGAGCAGCTGATCCCGTCGGACGCGGTGCTCGCGGCGGTCAGCGAGCGGCTCGACGAACGGCGCCTGGTGGGAACCCGGTTGATCGTCGAACCGCCCGCCTACCAGGGCGTCACGGTGGTCGCCCGGCTGGTGGCAGCTCCCGCCGACGTGGACCGGGTGCGGGCCGAGGCGCTGGAGGCCCTGTTCCGCCACATCGATCCGTTGCGGGGCGGGGCGGACGGGCGGGGGTGGCCGTTCGGCAGGCCCGTGCAGTACGGGGAGGTCTTCGCCGTGCTCCAGAACGTGGAGGGGGCGGGGCTGGTGGAGGACGTCCGGCTGTTCCCGGCGGACCCGATCACGGGCAGGCGCGGGGCGGCGGCGGACCGGGTCGACGTGGCGCCGGGCGCGCTGGTCTTCTCGCACCAGCACCAGGTCGTGGTGACCGCGAGCGGGGCCGGTGAGGCCGTATGACGCGGGCGGCGGTGCCCGGGCTGCCCAGCCGCTACCCGATCGGGGAGCTGCTGCCCGCCCTGTACGCGGACGACGACCTGGCCCAGCGGTTCACGGCGGGCCTGGACACGGTGCTGGCCCCGGTCCTGTCCACGCTGGACAACCTTCCCGCGTACGTCGACCCGGCGCTCGCCCCGGCCGACTTCCTGCCGTGGCTGGCGTCCTGGGTGGGCGTGGAGGCCGATCCGGCGTGGCCGGTGGAGCTGCGCCGGGCGGTCGTCGCGCACGCCGTCGAGCTGCACCGGTGGCGCGGCACCCGGCGGGGTCTCGTGGAGCGGCTGCGGCTGGTCTGCGGAGTGCACGCGGAGGTCCGGGACGGCGGGGGCGCCACCTGGTCGGCCGAGCCGGGGGCCGCGCTGCCACCGCCGCCGACCGGTGAACTCCTGGTGCGGGTCTGGCCGGTGCGCGCGGGCGACGGGGCGGACGCGGTGGACGCGCACCGTGTCCTGGAGGTCGCCACCGCCTCGTGCCCGGTGCACCTGACCTGCCGGGTGGAGGTCCTGCCGGGCCCGCCCGAAGAGACTGGAGACTGA

Protein sequences of DBSCAN-SWA_1

>NZ_CP010833|2178113:2203908|2193629_2194133_+|WP_075264136.1|DBSCAN-SWA
MRRRTVTPGAGLEETLDNLAAATATRQEAPAAAAPARAPRRERDTLQTEFAFELPRGYVDDEGQVHRNGTMRLATARDELKPQIDLRVKENPAYLSVVLLAQVITQLGPVTDVHTGIVERMYATDVAFLQDFYRRINSEGHTHAAVTCPLCHGSFEVDLSGGRLGES
>NZ_CP010833|2178113:2203908|2203332_2203908_+|WP_075264143.1|tail|DBSCAN-SWA
MTRAAVPGLPSRYPIGELLPALYADDDLAQRFTAGLDTVLAPVLSTLDNLPAYVDPALAPADFLPWLASWVGVEADPAWPVELRRAVVAHAVELHRWRGTRRGLVERLRLVCGVHAEVRDGGGATWSAEPGAALPPPPTGELLVRVWPVRAGDGADAVDAHRVLEVATASCPVHLTCRVEVLPGPPEETGD
>NZ_CP010833|2178113:2203908|2200599_2200917_+|WP_075264140.1|DBSCAN-SWA
MPPAARTGDSTAHGGLIGTPPPGALAVATVLIGGRPAAVTGSLHGCVVPPHAALGPGNVIMPNPAAAIGGAVLIGGLPAARMGDKTTCGAPIVSGAFNVLIGSPM
>NZ_CP010833|2178113:2203908|2189501_2190815_+|WP_075264134.1|DBSCAN-SWA
MTVSPGGTATTTLTVRNDGDIVEAYTLEVVGDCAAWTTAEPARVSLYPGTSETVTLTFAPPRSHEVRAGETPLAVRVLPAERPESVVVPESTVTVEPFHELRAELEPRRRRGWLGARFRTAVQNKGNTPVDVALAGRQDGEDLRLAFTPDKKRLEPGESAEVALKVRARKLIWFGEPVAWPFEVLATEGGEGDAEAGTAAEAAQPGEAEPLPGEFAQIPVLPKWLLIVLAALLALLLAWFALVRPAVQSTAKQAGAKAAQEETERGKEQGSTPPGGAENPAGGQGQGTGPDGTGPGGTGSGPGSTGGGGSTGGSGGSGGEQASRTIDVQTRAGAEGEGTYKVPAGKVFRVTDVVVANFQGDEGLVTISFGENKITTIALETFRNQDYHWVTPIQVPENATVTASVTCAKPGTPATGTQASGCHQVLNVSGVLSDLAR
>NZ_CP010833|2178113:2203908|2201374_2203336_+|WP_075264142.1|plate|DBSCAN-SWA
MALPSPNLDDRRFQQLVDEAKRFVQQRSPEWTDHNVSDPGVTLIETFAYMVDQLLYRLNRVPDKNYAAFLDLLGVTLFPPTVARADIDFWLSAPQPETVHLPAGTEVATARGEAEEPVVFSTSEDLPIVPSSLERLVTAPVSGEQTDRTAPLGAGKDIPCFQARPEPGDALLFGLPTAVPRCIVAVRLDSRVEGVGVDPRQPPLVWEAWDGARWVVCATGTDSTGGLNRPGEVVVFVPAGHTASVVAGTRAGWLRCRVTAPEPGQPFYSESPTIREAEVFTVGGTTAAEHAETVLDVPLGVSEGVAGQRFLVSRAPLLLDGDPPVVQVSTDEGWEIWTPVEHFGASGPGDRHVRVDAVAGEFAFPPEVREPDGTMRAYGAVPAKGAQLRVPRYRTGGGSAGNVARGAISVLRSSVPYVAGVNNREAATGGVDGETVENAKVRAPTILRVQERAVTAEDYELIAREAAPSLRRVRCLPAVPGEAGAVRVLVVPDAVADEDGQVRFEQLIPSDAVLAAVSERLDERRLVGTRLIVEPPAYQGVTVVARLVAAPADVDRVRAEALEALFRHIDPLRGGADGRGWPFGRPVQYGEVFAVLQNVEGAGLVEDVRLFPADPITGRRGAAADRVDVAPGALVFSHQHQVVVTASGAGEAV
>NZ_CP010833|2178113:2203908|2193192_2193633_+|WP_006127703.1|tail|DBSCAN-SWA
MAEGDALSTHVFGVQLGGYLVESIQEISGMTVEEEVVEVRQVTADGKQIIRKQPGARQAGEVTITRGLDKSSEFTTWIKETLNNGAVDTARQNLTIEIKDSTGETVRRIQLMQGWASKWEGPSLKAGESSAATETVTITFEEIVVE
>NZ_CP010833|2178113:2203908|2188542_2189265_-|WP_075264133.1|DBSCAN-SWA
MTITETTNSTAARGQYRRPDAAGRRTTGAGGAPGGRVSVAVYAEDLILQTGMIHQLRVRPEIELLPEAEADRAQVSLVVVDTVGETTVQLLHRLQRNTSTRTGLVVGYFESGALQTMIECGVAAVLRRGEADQDRLVHLVRAMANGEGVLPGDLLGKLLDHVSSLQRTVLDPRGLTLSTLTAREAEMIRLVSEGCDTAEIAQKTSYSERTVKNVLHEVATRLELRNRAHAVGYAMRHGLI
>NZ_CP010833|2178113:2203908|2196055_2196550_-|WP_159027415.1|DBSCAN-SWA
MDAEVDVDVDGGAVPAEPCAAAVRSRGTGRIRTGGGGVVVTAERWTGAGAGAGPDGSAGPLVTAGADLTGIAAGSLGGVAAGAGTVAPEPGVAAGPEPGARSVFGCVTVDGRSPSSGAPPSSRAVGGSEGSGAPIPPRTRADVFGPGAGARCTEGEGSDGFDDG
>NZ_CP010833|2178113:2203908|2196992_2197478_+|WP_079181606.1|DBSCAN-SWA
MVRPRPPAPRPADAAPVPVQRQAMPVVPDGAGPPAAGPAPVGGAAPGGPPSPSVRVPPRPAAQGAGPGRPETRAQAVQRAAANAGITGVPVQAAPAKPAAGATGAATGPVDASDASSPANRLSGTEIEELARRLLDPVSRLIRADLRRGRERSGRLHDGRR
>NZ_CP010833|2178113:2203908|2198757_2200542_+|WP_075264139.1|DBSCAN-SWA
MSGKDSPGRSFAADPIVEAPAELPAAWATQLVSCVVDENVGLPDTAVLMYRDPDHTFLSRTGIGMGTPLKISVVTVKDRARERLFTGEVTAVELDTDTTGSFTVVRAFSKAHRLQRGRKVMAYRNMKTADIVRKVAAGAGLAVGRIEAAPVTYKQLTQPNVSDWEFLQHLAAESGATVRVDDKGLLQFTKPDPASSAPSPSTSATRDPMVLEYGNNLLALRAVLTGADGSDSVEVRGWNVDTKTRLVARQQSVRSDTVAPGMSPSDAARIFGSGGSRTTIADTPYRTQAETRAVAGALAASVSAGFGEVEAVAYGNPQLRAGLPVALGNVGPAFSGRYTATAAHHVLEPDTGYRTTVIVSASPDRSLSGLTAGANAPSRGPRMPGLAIGVVTDIREEGKGQRGWVRLKFPWLDDTYVTDWVRTVQWGGQGGGGVFSPEVNDEVLVGFEQGLLDSPYVLGGLYNGVDKPSPHDVPLVDPTSGKVNRRSLVSRSGNRLELLDAPRGPAGVRIATGDKRLDVVLDEKKGEITLTVKARGGGRELSSVTLSASGITLDAGATGDVNIKGRSVTVNGKTGVTVDGGLLAVLKAKLIRIN
>NZ_CP010833|2178113:2203908|2180980_2182237_+|WP_075264129.1|DBSCAN-SWA
MTPTEPASALGVHSEVGRLRKVLVCAPGMAHRRLTPTNSDDLLFDDVMWVENAQRDHADFVNQLTERGVEVVELHALLAATMEIPEARTWLLDRKIDANEVGLGLVDDTRAFLDALTPRRLSDHLIGGLAIADLPEEFRSAYVGLAREGTGAREYLMPPLPNTLYTRDTTCWLYSGVTLNPLYWPARHDETLLMKAVYTFHPDFRGSRIWWGDPEKDWGRATFEGGDIMPVGNGVVLMGMSERTSRQAITQVAAALFAQGAAEHVIVAGMPKLRSAMHLDTVFTFADRDIVTLYPRIMDAVHTFSLRPSDRAPGIEITDEGSTPFTEVVARALGLPQLRVIETGGDVYASERQQWDSGNNAVALEPGVVFTYDRNTQTNALLRRAGVEVITIVGAELGRGRGGGHCMTCPLIRDAVAF
>NZ_CP010833|2178113:2203908|2182334_2184458_-|WP_075264130.1|DBSCAN-SWA
MTPAVEQASQQHELTDIEVLWERLGHVEQRVREAVAARRAVDPDPDDPYRGQYLTPEAAARILESRDAFTPVPAYGDGAPTGAGDGGRLDELAERFGLAPLDVDLLLVALAPDIDPRFERLYGYLNDDLTRRRPTIGLALELCGLPAAGAGRFRFAPAAPLVAGGLLEIAEPERPLLSRLLCVPDRVTAYLLGDDGIDGRLRGIVREDTRPPEPDERPEVPRVAAVLGAGSGLVHLLDRGGDPHGLAIAALHTAARRPLVVDLAALATAPEPASLVQALATESRLGRAGVVLGPLETLAPERPEGARLLGSLCAALGSTPLIAYGKKNWDPLWTAESPVPVTVPPPGPDGMARQWRRALAEAGRSVGLSAAHATAGDALVEAAAAYRLDSGQLRRAATVASRLAVLEPRPVSPEDLRAAVRAQNGAGLERLARRIEPGVGWADLVLPPSTRTQLTELALRARHRETVLGQWRMRPGGGRGRGVIALFAGESGTGKTMSAEVVAAELGMELYVVDLSTVVDKYIGETEKNLERIFVEASDVNGILLFDEADAIFGKRSQVNDSRDKHANMESAYLLQRMESFDGIAVLTTNLRANLDEAFTRRLDVIAEFPMPDARQRLALWDRCLGPAVPRDATLDLEFCADRFELAGGSIRACAVTAAYLAAESRAPLTMDQLVTAVLQEYRKLGRLVLESEFGPWLAKERARAGR
>NZ_CP010833|2178113:2203908|2198038_2198761_+|WP_075264138.1|DBSCAN-SWA
MSPALRASRARAQLTVMEPPSAVGAKPGGTLARLTLQFNPAKLSLSKSTEWRRTPSRMAGQSALPEFVGSGPRALSLEVFLDATATHDNSVEKAVEQLMTACVPTPSSLARKTPASPWVRFDWGTSKTTSFDGVLSNLSVSYTLFDVDGKPLRATCSLSIEEASVDPAGQNPTSGSKEARRTHRVVAGDSLPLLAWREYGDATAWRTIAHANDIDDPMRLTPGQELLVPGREDHPAEGGR
>NZ_CP010833|2178113:2203908|2178113_2179313_+|WP_075264127.1|protease|DBSCAN-SWA
MRNTRKFSLAAAGVLLSAATVLGTQSMAQAQDGAATPRYQPEMVEALAASLGVSEKAAVDRLDRQDAQQAKLAGLQKRGISGDGAFFDASGRLTVNADDHAEAARIEQAGLDARVPARGQAALDRIKAELDRLAAATTPSGVVAWSVDLPSDQVTVKVNNERGAAAKAFLAKAAEHGSAVRIVRGEEKLEAKAAIYPGSKMTFNNTTQWCSVGYGARDSSGRQYLVTAGHCVTNTLRYDGAAFAQGYKTRYALGTRSVDMGILTINSGHSITTSVGTWGNSNPVAVRGGTRASSGAAVCKSGATTGWTCGTIGSYNNTVTYVDLNGGPDTVVSGLATSSVCVEGGDSGGAYISGNQAQGMTSGGPTNQRCTGGVNSRGSSYFQPLDDTLRYYGLTLNTN
>NZ_CP010833|2178113:2203908|2200913_2201375_+|WP_075264141.1|DBSCAN-SWA
MSGDGYAGRGGGFIGRGWGFPLRTGPTGGIALVERDKEIEEAIGLILGTAPGERPMRPEFGCGIHEYVFAPGDGATAGRIAHEVRTSLERWEPRIEVTDVVVAFDAVEEGTLYIDVHYTVRATNDLRNLVFPFYTIPSSEGSAARSAPEAGRL
>NZ_CP010833|2178113:2203908|2179481_2180921_+|WP_107472787.1|DBSCAN-SWA
MSHPEAPPRPAAKLSLLTLTAMVVGSMVGAGVFSLPSRFAQETGVAGALIAWAVAGTGMLMLAFVFQALAVRRPDLDAGVYAYAKAGFGEYLGFFSAFGYWASACVGNVTYWVLIMSTVGAVAPVLGDGDTVTAVVVSSVGLWGFFLLIRRGVKEAAAINRIVTVAKVVPILFFVVLALFCFEPSVFADNFSGTAEAGTLFDQVRGTMLATVFVFLGVEGASVYSRHAKRREDVGRATVLGFLSVFAVFASVTIVSYGLLPMAEIAELRQPSMAGVLASAVGTWGKVFISVGLVVSVLGAYLAWTLMAAEVLFVAARDKDMPRFLGQSTAADVPENALLLTTCLSQLVLVVTLFSDDAFAFALDLTSALSLIPFLLAAAFAVKVAARPERWGAVGRSARRELVIAVVATLYTAFLLYAAGPKFVLVSFILYAPATFLFVKSRREQGRRVFSPGEAVICAVSVAGAAVGIAALALGWIEL
>NZ_CP010833|2178113:2203908|2184454_2185159_-|WP_075264131.1|DBSCAN-SWA
MIHEVDEGLRLLLAEAGLEDSGVDLVFDAPTKDWSARRNAPTISVFLHGIREDAARRRTGTAETHDEEGVITGWRTPPRWFELTYLVTAWTNRPQDEHRLLSEVLRTLVRTDTLPARLHTGSLAELGLTVELEAAGPGAGGPSASDVWSALGGELKAAIDLRVLAPLAGERTAAGPPVTEGLVMQAAPHLDGGPGDPGRRLRYDGATDPGGQGFAAPRERRLPPGRRRRGNAAR
>NZ_CP010833|2178113:2203908|2185155_2188413_-|WP_075264132.1|DBSCAN-SWA
MTGTAGPAKHSRLGRLTGAVVLLAPLLLVGSAAAPDGAGQAVAAPADADPAQAGRIAFAGTDHRSLGRANDQDRTDPLFGDGPAHYDQDPSARGDVLVFTSLRDSAKPQVYLRGADGSVRRLTEGRDAARPELSPDGRTVVFDSAEPGPGGTVQRDLWSVGVDGSNLRRLTDTADNEESPTWSPDGTRIAYACDGDTALGWQIYVRDVAGGPQTRISDAGAGDATEPSWNPGADPAVRNIVAYTLTTNPDPNVDDGTELRATEGLGTDRPLLAGGHAEWGTRSASWLPDGKDVVFLSPYHTCGCDDFDHVYRVTAFDGAKEPEQLVDENREVGPPTWFPPAGTVVVPRITPDPETVKQEDEVLSAAQVVTLQDVRQDGSDPRDLGLTILKEDPEARTNQDAAVDRLFNPRPGFDPWTERQSYTPDGRRIVVTRFEDTDAGRVERIWMADADGGNAAALPLAGRGPNDWDTDPAFSPDGTRLAFTRTSPGGTGDAAGPSRILVADVASGEILDEIRPPAGQQTGGDAQPTWSLDGDNLAFTRNHVINGNGGNKHIWVVPVADLGNQRDLSATICPGACDVIDDSPAFSPDGLKVAFNRKDGGGRVNQQAGVIVKPLSGGGCRVVLPSVQKDNPAGCDLPIPDTSATGPHQPRDVAWTPGGDRLVFSARRELAPNSMEQLSVLDLASGELTPVDNAHAGRQKEPALQQSVDLSLTAPPNRPAVEVGSETEVTITVTNRGPAPSPGTTLTVDAPPGVRLEELTTDTATCAPGTPQCDLGTVPPGTDVEITARLTGVTTGIQRVNWSVTGTVIDPNPTDNATGTIVPVEDAPPPTPPPTAPPPSPTPTPTTPAPTPPPTTTPPPPPAPAPPPPAPEAGPAVTVRAQPSPGYVGGKVVVTYTVRNGRNALATGLRLDLGLPRGIPAGPLPAGCAAGACTIPDLAPRASTVISVVLSPDKALRTTITASLTTTGTDANLRDNVSRIPLRILQPRIIAVPKVGKPGFVTSVRGKDFPPGAPVTLSWKPGITAAAAPTRPLGDGTFIAQLLILAKDEIGPRDITAKGPGFSPVKTDFLVVLGTITPPDEVIRR
>NZ_CP010833|2178113:2203908|2197563_2197989_+|WP_075268297.1|tail|DBSCAN-SWA
MTDNIFATSVFFKLAIGGSDLGAFHTCSGLGAEVEMETYAEGGNNGFTWQLPGRITWTNITLTRPVTTDTLKIARWLNETIQRVEPKDGEIVALRPDLSRIISWQVHGIVPVRWQGPSFDPANSEAAIETLEIAHEGLEPS
>NZ_CP010833|2178113:2203908|2191588_2193130_+|WP_075264135.1|tail|DBSCAN-SWA
MPSYLTPGVYVEEVQSGARPIEGVGTAVAAFVGFAGTGPFHRPTLVTNWDQYVQTFGAFTADTYLAHAVYGFFANGGGAAYVVRIGGPAEGADTTGQGSVAQAPAPVALGGFLVAAKPGTGDGLSVEIADAEGENPPEDRFRLLVRQGGKAVETYDVSTRKNVKGYLVTQARDSKLIQVTEQPGTAQSRPEKQTVALAPATAAAPGNGVARLDASEYVGDASARTGFAGLEAIDEITMVAVPDLMSAFQRGDIDAEGVKTVQLAVISHCEQMGDRVAVLDTPPGMNAQRVRTWRNEDAGYDSRYAALYYPWVKVFDPASGRNSLVPPSGHVAGVWARSDNERGVHKAPANEVIRGAVDLEIRLSKGEQDLLNPIGVNCVRAFPGRGIRIWGARTLSSDPAWRYLNVRRLFNYLEESILLGTQWVVFEPNDDRLWSSIRRNVTAFLTEEWRRGALFGRTAEEAFYVRCDRSNNPQESIDLGQVVCEIGVAPVKPAEFVIFRLSQFSDSTSLVDE

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_075264127.1|2178113_2179313_+|protease	trypsin-like serine protease	NA	NA	NA	NA
WP_107472787.1|2179481_2180921_+	amino acid permease	NA	NA	NA	NA
WP_075264129.1|2180980_2182237_+	arginine deiminase	NA	NA	NA	NA
WP_075264130.1|2182334_2184458_-	ATP-binding protein	K9MCS8	Sulfolobus_virus	1.4e-06	28.3
WP_075264131.1|2184454_2185159_-	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_075264132.1|2185155_2188413_-	DUF11 domain-containing protein	NA	NA	NA	NA
WP_075264133.1|2188542_2189265_-	response regulator transcription factor	NA	NA	NA	NA
WP_075264134.1|2189501_2190815_+	hydrolytic protein	NA	NA	NA	NA
WP_075264135.1|2191588_2193130_+|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	1.3e-70	34.1
WP_006127703.1|2193192_2193633_+|tail	phage tail protein	NA	NA	NA	NA
WP_075264136.1|2193629_2194133_+	hypothetical protein	NA	NA	NA	NA
WP_159027415.1|2196055_2196550_-	hypothetical protein	NA	NA	NA	NA
WP_079181606.1|2196992_2197478_+	hypothetical protein	NA	NA	NA	NA
WP_075268297.1|2197563_2197989_+|tail	phage tail protein	A0A059XEM3	uncultured_phage	6.0e-05	31.7
WP_075264138.1|2198038_2198761_+	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_075264139.1|2198757_2200542_+	VgrG-related protein	NA	NA	NA	NA
WP_075264140.1|2200599_2200917_+	hypothetical protein	NA	NA	NA	NA
WP_075264141.1|2200913_2201375_+	GPW/gp25 family protein	A0A0E3F3H3	Synechococcus_phage	2.3e-10	38.6
WP_075264142.1|2201374_2203336_+|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_075264143.1|2203332_2203908_+|tail	phage tail protein	NA	NA	NA	NA

Sequences of DBSCAN-SWA_2

Nucleotide sequences of DBSCAN-SWA_2

>NZ_CP010833|6465732:6472579|DBSCAN-SWA
AATGAGCGAGCAGCCGGATCAGGAGCGGGACGAGGGCGCGGTCGCCTCGCTCGACCTCAAGCCCGCCCTGGAGGCGGTCCTCATGGTCGTCGACGAGCCCGCCACCGTCGACCACCTCGCCAAGGTGCTCCAGCGGCCCCGCAGGGCCGTGGCGGACGCGCTGCGGGAGCTGGCCGACGAGTACACCGTGCAGCGCCGGGGCTTCGACCTGCGGCTCGTGGCGGGCGGCTGGCGGTTCTACACCCGGCCCGCGTACGCGGCGGCCGTGGAGGGCTTCGTCCTGGACGGCCAGCACGCCCGGCTCACCCAGGCCGCGCTGGAGACCCTGGCGGTCGTCGCGTACCGGCAGCCGGTGAGCCGCTCGCGGGTCTCGGCGGTCCGCGGAGTCAACTGCGACGGGGTCATGCGGACCCTCCTCCAGAGGGGCCTGGTGGCCGAGGCGGGCGCGGAACCCGAAACAGGTGCGATCCTGTACAGGACGACGAACTACTTTCTGGAGCGAATGGGCCTGCGCGGCCTGGACGAGCTCCCGGAGCTCGCGCCCTTCCTCCCGGAGGCGGACGCGATCGAGGCTGAGACGCTAGAGGGTGTGCCGTCGTTCGATCCGGACGCACCGGACACCCCGGATACTCACGCAGACGACAAGACGGAATTTTGATGCGAAGCAGTGGCAGGAACAGCGGAAGCGGCAGCGGCGGTCAGGGCGGCCGGAGCGGCGGCCAGGGCGGCCGTCCCGGCGGTCAGGGCGGCGGCGGGCGCGGCCAGGGCGGCCGCAGCGGCGGCGGATCCTTCCGCCAGGGCCAGGGCGGCGGTCAGGGCGGACGCTCCGGCGGCCAGGGTGGCGGCGGACGCGGCGGCAGCGGCCAGGGCGGGCGTTCCGGCGGCCAGGGCGGCCGTCAGGGCTTCCAGGGCGGACGCGACGAGCAGGACCAGCGCCCCCGCCGTCCCCGCCCGGAGGAGCGCCGCTACGACGTCGGCAACGACGCCCCCGGCGCCCGCGGAGGCCAGGACGGCCCCCGCAAGGGCCGTGGCACGGCGGCCCGTGGCGGCGCCAAGGGCGGCCCGAAGTCCGCACAGGGCGGCAGCGGCGGCGGCTTCCGGCGCGGCGGCTCCCCCTCGCGCCCCCGCGAGCTGGACGCCAAGATCGAGCAGCGCAACCGCGACCGGTACGCGAACAAGCCCGACATCAAGCTGCCCAAGACCCACCCGGGCGCCGAGCAGGAGGGCGAGCGGCTCCAGAAGGTCCTCGCCCGGGCCGGCATGGGCTCGCGCCGCGCGTGCGAGGAGCTGATCGAGCAGGCCCGCGTCGAGGTCAACGGCGAGATCGTCGTCGAGCAGGGCATGCGCGTCGACGTGCACAAGGACGAGATCAAGGTCGACGGCCTGACCGTCGCCGCCCAGTCGTATCTCTTCTTCGCGCTGAACAAGCCCGCCGGTGTCGTCTCCTCGATGGAGGACCCGGACGGCCGCCAGTGCCTCGGCGACTACGTGAACAACCGCGAGACGCGGCTGTTCCACGTCGGCCGGCTCGACACCGAGACCGAGGGCATCATCATGCTCACCAACCACGGTGAGCTGGCCCACCGCCTCACGCACCCGAAGTACGGCGTGAAGAAGACCTACCTGGCCGCCATTCAGGGCCCGCTGCCGCGCGACCTCGGCAAGCGGCTCAAGGACGGCATCCAGCTGGAGGACGGCTACGCCCGCGCCGACCACTTCCGGGTCGTCGAGAACACCGGCAAGAACTACCTGGTCGAGGTGACCCTCCACGAGGGCCGCAAGCACATCGTGCGCCGGATGCTGGCCGAGGCCGGCTTCCCGGTCGAGCGGCTCGTGCGGACGTCCTTCGGGCCGATCCCGCTGGGCGACCAGAAGTCCGGCTGGCTGCGCCGCCTCACCAACACCGAGGTCGGCATGCTGATGCGCGAGGTCGGTCTCTAAGAGCTCCCCGTCAAGGCCCGCGGCCGGTAGCTGTTCGGAAAGTTCGAACAGACCCGGCCGCGGGCCTTTTGCTGCCCCCGTCCAGCCTTTATAGTCAGAGTGACTATAAAGAAGGAGGCGGGCCCGTGAGCCTCGCGGAGATACTCGATCCCCTGCAGCAGCCCCTGGTGACGGTCCTGGACACCCCGGTCAGCTGGACCGAGGTGCTGGGCTTCGGCAGCGGGGCGCTCTGCGTCTGGCTCGTGGCCCGCCAGCACATCGCCAACTGGCCGATCGGCATCGCCAACAACCTCTTCTTCATCCTGCTGTTCACCCAGGCCGGCCTGTACGCCGACGCCGGCCTCCAGATCGTCTTCATCACCCTCGCCGCGTACGGCTGGTGGACCTGGACCCACGGGGGTGGACCAGGGACCTCGGTCCTGCCGGTGCGCAGGACGACCCGCACCGAATGGGCCTGGCTGCTCGCGGCGGGGGTGGTGGGGACCGCGGCGATCACGCTGCTGCTGTCCCGGGCCACCGACTCCACCGTCCCGTTCTGGGACGCCCTGACGACGTCCCTGTCGCTGATGGCGACGTACGGGCAGTGCCGGAAGCGGCTGGAGTCCTGGTGGCTGTGGATCGCGGCCGACGTGGTCTACATCCCGCTCTACGCCCACAAGGGGCTGTATCTGACCTCGCTGCTGTACGCCGGGTTCCTCGCGCTCTGCCTGGTCGGGCTGCGCAACTGGCACCGCGACCTGACCGCACGCGAGGCCCGGACCCCGGAGGTGGCCGCCGTATGAAGCGCTACGAACACGCCCTGGTCCTCGGCAAGTTCTACCCGCCGCACGCCGGGCACCACCACCTCGTCCGGACCGCCCAGGACCGCTGCGAACGGCTGACCGTGCTGGTCTGCGCGGCCTCCGTGGAGTCCGTCCCGCTCGCGGACCGGGTCGCCTGGATGCGCGAGATCCACCCGGATGCCACGGTGGTGGGCGCGGTCGACGACACGCACATGGACGTCAACGATCCGGCTGTCTGGGACGCGCACATGGCCGTCTTCAGAGCGGCCGTGCCCGAGCGCGTGGACGCGGTCTTCACGTCGGAGGCGTACGGGGAGGAACTGGGCCGCCGCTTCGGTGCGGACTCCGTGCTCGTCGACCCCGACCGCACCCTCTTCCCGGTCTCCGGCACCGCCGTCCGCGAGGACCCCGTCGGCTGCTGGGACTTCCTCCGGCCGCCCGTACGGGCCGGCCTCGCCCGCCGCGTCGTCGTCCTCGGCGCGGAGTCCACCGGCACCACCACCCTCGCCCGGGCGCTCGCCGCCCACTACCGGGCGCGCGGCGGGGTGTGGGCGCGTACCGGCTACGTCGCCGAGTACGGGCGCGAGTACAGCGAGGACAAGCTCGCCGACCTGCGCGGGCGGTGGCCCGGGGCCGCCTGGGAGGACGTCACCTTCACCACCGACGACTTCCCGCTCATCGCGCGGACCCAGAACGAGCGCGAGGAGGCCGCCGCCCGGGCCGGGTCCCCGGTGCTCTTCTGCGACACCGACTCCTTCGCCACCACCGTCTGGCACGAGCGGTACGTCGGCGGCCGCAACCCCCTCGTCGAGGAGATCGCGGACCGGGCCGACCACCACCTGTGGCTGCTCACCGACCACGAGGGCGTCGCCTTCGAGGACGACGGGCTGCGCGACGGCGAGGAGCTGCGCCCCTGGATGACCGACCGCTTCCGCGCCGAACTCACCCGCACCGGACGCCGGTTCATCGAAATGACCGGCCCGCCCGAGACGCGGCTCGCCGCAGCCGTCGCCGCCGTCGACGGACTCCTCGCCACCGGCTGGGAGTTCGCCGCACCCCTCCCGGAGAAACGATGACCACCCCCGCCCCCGAGGGCTACGACCCGCACGCCTACGCCCCGTTCGCGGTCACCGTCGACCTCGCGGTCTTCACCGTCCGCGAGGCCCGGCTGCACGTGCTGCTCGTCGAACGCGGCCAGGAGCCCTTCCGGGGCCGGTGGGCGCTGCCGGGCGGCTTCCTGCTGCCCCGCGAGTCCGCGGACGACGCCGCCCGCCGCGAACTGGCCGAGGAGACCGGCCTCGGCCCCGGCACCGTCGGCGCCCTCCACCTGGAGCAGCTGCGCACCTACACCGACCCGGACCGCGACCCGAGGATGCGAGTCGTCTCCGTCGCCTACGCCGCCCTCCTGCCCGACCTCCCCGAACCTCGCGGCGGCGGCGACGCGGCGAGCGCCCGGTGGTGGGACGCGGACGCCGTGGGACCCCTCGCCTTCGACCACGACACGATCATCGCCGACGCCCGCGACCGGATCGGCGCCAAGCTCGAATACAGCTGCCTGGCCACCGCGTTCTGCCCCGCCGAGTTCACCCTCGGCGAGCTCCAGCAGGTCTACGAGACCGTCTGGGGCGTCGAGCTGGACCGGCCCAACTTCCGGCGCAAGGTGCTGAGCGCGCCGGGCTTCGTCCAGCCGGTCGGCGGCCCGCCGCGCCGCACCGGCGGCCGGGGCAAACCCGCAGCGCTCTACCGGGCGGGCGACGCCACCGCCCTGCACCCGCCGCTCCTGCGCCCGCCGCGCACCGACGCCTCCCTCTCCTCTTCCTCCTCCGCAACGGAAGGACACGACCGATGACTCTCGCCATCCCGCCCCTCACGAAGCAGGCCGCGACCGGCGTCCTGACCGGGCTCGCCCTCGGCGACGCGCTCGGCTTCCCCACCGAGTTCAACGACGTGCCCTCCATCCTCGCCAAGTTCGGCCCCTGGCGGCAGATGCCCCTCCTGGACCCGGCCGTGGTCTCCGACGACACCCAGATGACGATCGCGCTGGGCCGCGGCATCCGTACCGCCATGGACAGCGGGCTGCTCACCCCCGAACGGATGGTGGGCCCGGTCAGCGCCGAGTTCATCGCCTGGTACCACGCACCGGACAACAACCGGGCCCCCGGCAACACCTGCCTCACCGCCTGCCGTCTGCTGGAGAACACCCGGATCTGGCAGCAGGCCAGCCAGACGCACTCCAAGGGCTGCGGCGCCAACATGCGGGTCGCCCCCGTCGGCCTGGTCCCCGGCCTCAGCGAGGAGCAGCGGGCCGGCGCCGCCCAGCTCCAGGCCGCCCTCACCCACGGCCACCCCACCGCCCTGGCCGCCTCCGACCTGCTGGCCCGCGCGGTGTTCCTGCTCGCCCAGGGTGCCGAACCCCTCGGCCTGATCGGGCAGTTGCGCAGCTACGCCCTGGAGAACCGGGGCCGCTACCACACCCGCTGGCTCGGCGACCTCTGGCGCCACGCGGGCGACGCCACCCCGCAGGCGTACATCCAGCGCGGCTGGGACGAGTGCCTGGCGGCCCTGGAGACCGTACGGGACGCGCTGCGCGACCCGTCGCCGGAGACGGACCCGTGCGAGCGGACCGGCGACGGCTGGATCGCCGAGGAGGCTCTCGCCACCGCCCTGCACTGCTTCCTGCTCTTCTCCGAAGAGCCCGTCACCGCCCTGCGCCGGGCCGCCTGCACCCGGGGCGACTCGGACTCCATCGCCTGCCTGACCGGAGCGCTGGCCGGGGCCCACCTGGGCGCGGCGGCCTGGCCCAAGGAGTGGTCCGAGCGCATCGAGTACCGCAGCGACCTGCTGTCCCTCGCGGCGCTCTGGGACGCCTGACCGGCGGGGGAGGGGGTACGAGAGGGCGGAACCCGTTCCCGTACGAAGGCCTGGTGGTATCCGTGTCCTCCTCACTCGTCGAGACCGTCGACATCAAGGCCCCGGTGGCCGTCACCTGGTCCCTGTGGAGCGACGTCACCCAGTGGCCGCGGTTCCTGAGCCACGTCCAGCGCGTCGATCCGATCGACGAGCGGCGTTTCGCCTGGCAGCTCTCGCTGCCCGGCGCGGACAAGAACTTCGTCGCCGAACTCACCGAGGTGGTCCCCGAGGACCGCATCGCCTGGAAGACGGTCGAAGGCGTCCACCACGCGGGGGTGGTCACCTTCCACCGCCTCGACGACACGTCCAGCCGTGTCGCCCTGCAGATCGAGTACGACCCCCAGGGCTTCGTCGAGCGCCTCGGGGCGCTGACCAACCTCGACTCCACGCTGGCCAACTACGACCTGGGCGAGTTCCAGAAGCTGGCCGAGCTCACGGCCGAGGCGGGCGGTCCCCGGACGCTCTGAGCCCGTCAGGGGCCTCGGGGGTGTCTTGCCGATCGAGCCGGGCTCGTGTGCCCTAGCTCCGCGCCGCCGAGGCCCGCCGGGTCCGGACGAGGAAGTCCTCCACGGCCGCCCGGTCCGGCTCCGCCGGCAGCGGGGAGCGGGCCGCCGCCTCGTCGTTCTCCTCGCCGAGCCGGTCCATCCGGCGCTCCACCTCAGCCCAGGACACCTCGCCCCGCTTCACCGCCAGCAGCTCCTCCCGGGCATCGCCCACGTCGATGCGCAGCTCGCCCGTACGCAGCAGGTCCCGGCTGCTCGCCAGCAACCGCAGCAGATGCATCGCGTGCTTCCAGCGCGGCGCGCCGTGCACCCGCACGTCCGCCGCCAGCTTTCTCCGCTGCCCCAGCGCGTACCGGACGAACGTGCCGTGCGCGAGCCGCGACAGGAACGCCCCGCGCAGCGCCAGCAGCTCCCCGCCGGTGTCGTCCACGGACTCCACCAGCGGGGAGTGCAGGCACTCCAGCACGTTCGGGTTGGCCCGGAGCGCCAGCTCGCAGAAGCGCTCCAGCTCCCAGGAGAACTGCTCCGGCGCGGGCCCGTCGACATGCGTCGGCGGCTTCTCGAACCGCCAGAACAGCTCCGTGGGCGCGAGGAACACGCCGCGCCGGTCGGTGTCGCTGTCCTCCGTGGCCAGTCCGAACGCGCGCGAACCCATCACACAGGCGTAGACCGTGTGGTCGCGTACGAGTGCCTCGTCGGTGGCGGTGACCAT

Protein sequences of DBSCAN-SWA_2

>NZ_CP010833|6465732:6472579|6467797_6468454_+|WP_075267093.1|DBSCAN-SWA
MSLAEILDPLQQPLVTVLDTPVSWTEVLGFGSGALCVWLVARQHIANWPIGIANNLFFILLFTQAGLYADAGLQIVFITLAAYGWWTWTHGGGPGTSVLPVRRTTRTEWAWLLAAGVVGTAAITLLLSRATDSTVPFWDALTTSLSLMATYGQCRKRLESWWLWIAADVVYIPLYAHKGLYLTSLLYAGFLALCLVGLRNWHRDLTAREARTPEVAAV
>NZ_CP010833|6465732:6472579|6468450_6469530_+|WP_075267094.1|DBSCAN-SWA
MKRYEHALVLGKFYPPHAGHHHLVRTAQDRCERLTVLVCAASVESVPLADRVAWMREIHPDATVVGAVDDTHMDVNDPAVWDAHMAVFRAAVPERVDAVFTSEAYGEELGRRFGADSVLVDPDRTLFPVSGTAVREDPVGCWDFLRPPVRAGLARRVVVLGAESTGTTTLARALAAHYRARGGVWARTGYVAEYGREYSEDKLADLRGRWPGAAWEDVTFTTDDFPLIARTQNEREEAAARAGSPVLFCDTDSFATTVWHERYVGGRNPLVEEIADRADHHLWLLTDHEGVAFEDDGLRDGEELRPWMTDRFRAELTRTGRRFIEMTGPPETRLAAAVAAVDGLLATGWEFAAPLPEKR
>NZ_CP010833|6465732:6472579|6470299_6471325_+|WP_075267096.1|DBSCAN-SWA
MTLAIPPLTKQAATGVLTGLALGDALGFPTEFNDVPSILAKFGPWRQMPLLDPAVVSDDTQMTIALGRGIRTAMDSGLLTPERMVGPVSAEFIAWYHAPDNNRAPGNTCLTACRLLENTRIWQQASQTHSKGCGANMRVAPVGLVPGLSEEQRAGAAQLQAALTHGHPTALAASDLLARAVFLLAQGAEPLGLIGQLRSYALENRGRYHTRWLGDLWRHAGDATPQAYIQRGWDECLAALETVRDALRDPSPETDPCERTGDGWIAEEALATALHCFLLFSEEPVTALRRAACTRGDSDSIACLTGALAGAHLGAAAWPKEWSERIEYRSDLLSLAALWDA
>NZ_CP010833|6465732:6472579|6466388_6467672_+|WP_075267092.1|DBSCAN-SWA
MRSSGRNSGSGSGGQGGRSGGQGGRPGGQGGGGRGQGGRSGGGSFRQGQGGGQGGRSGGQGGGGRGGSGQGGRSGGQGGRQGFQGGRDEQDQRPRRPRPEERRYDVGNDAPGARGGQDGPRKGRGTAARGGAKGGPKSAQGGSGGGFRRGGSPSRPRELDAKIEQRNRDRYANKPDIKLPKTHPGAEQEGERLQKVLARAGMGSRRACEELIEQARVEVNGEIVVEQGMRVDVHKDEIKVDGLTVAAQSYLFFALNKPAGVVSSMEDPDGRQCLGDYVNNRETRLFHVGRLDTETEGIIMLTNHGELAHRLTHPKYGVKKTYLAAIQGPLPRDLGKRLKDGIQLEDGYARADHFRVVENTGKNYLVEVTLHEGRKHIVRRMLAEAGFPVERLVRTSFGPIPLGDQKSGWLRRLTNTEVGMLMREVGL
>NZ_CP010833|6465732:6472579|6465732_6466389_+|WP_075267091.1|DBSCAN-SWA
MSEQPDQERDEGAVASLDLKPALEAVLMVVDEPATVDHLAKVLQRPRRAVADALRELADEYTVQRRGFDLRLVAGGWRFYTRPAYAAAVEGFVLDGQHARLTQAALETLAVVAYRQPVSRSRVSAVRGVNCDGVMRTLLQRGLVAEAGAEPETGAILYRTTNYFLERMGLRGLDELPELAPFLPEADAIEAETLEGVPSFDPDAPDTPDTHADDKTEF
>NZ_CP010833|6465732:6472579|6471387_6471831_+|WP_075267097.1|DBSCAN-SWA
MSSSLVETVDIKAPVAVTWSLWSDVTQWPRFLSHVQRVDPIDERRFAWQLSLPGADKNFVAELTEVVPEDRIAWKTVEGVHHAGVVTFHRLDDTSSRVALQIEYDPQGFVERLGALTNLDSTLANYDLGEFQKLAELTAEAGGPRTL
>NZ_CP010833|6465732:6472579|6471883_6472579_-|WP_075267098.1|DBSCAN-SWA
MVTATDEALVRDHTVYACVMGSRAFGLATEDSDTDRRGVFLAPTELFWRFEKPPTHVDGPAPEQFSWELERFCELALRANPNVLECLHSPLVESVDDTGGELLALRGAFLSRLAHGTFVRYALGQRRKLAADVRVHGAPRWKHAMHLLRLLASSRDLLRTGELRIDVGDAREELLAVKRGEVSWAEVERRMDRLGEENDEAAARSPLPAEPDRAAVEDFLVRTRRASAARS
>NZ_CP010833|6465732:6472579|6469526_6470303_+|WP_075267095.1|DBSCAN-SWA
MTTPAPEGYDPHAYAPFAVTVDLAVFTVREARLHVLLVERGQEPFRGRWALPGGFLLPRESADDAARRELAEETGLGPGTVGALHLEQLRTYTDPDRDPRMRVVSVAYAALLPDLPEPRGGGDAASARWWDADAVGPLAFDHDTIIADARDRIGAKLEYSCLATAFCPAEFTLGELQQVYETVWGVELDRPNFRRKVLSAPGFVQPVGGPPRRTGGRGKPAALYRAGDATALHPPLLRPPRTDASLSSSSSATEGHDR

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_075267091.1|6465732_6466389_+	SMC-Scp complex subunit ScpB	A0A1B1IVT7	uncultured_Mediterranean_phage	3.1e-08	29.7
WP_075267092.1|6466388_6467672_+	rRNA pseudouridine synthase	NA	NA	NA	NA
WP_075267093.1|6467797_6468454_+	nicotinamide mononucleotide transporter	A0A2I7SAC7	Vibrio_phage	1.3e-11	26.5
WP_075267094.1|6468450_6469530_+	AAA family ATPase	A0A2K8HHU5	Bacteriophage	8.1e-30	30.9
WP_075267095.1|6469526_6470303_+	NUDIX hydrolase	A0A0E3JJF3	Streptomyces_phage	2.4e-23	50.0
WP_075267096.1|6470299_6471325_+	ADP-ribosylglycohydrolase family protein	A0A2D0ZND4	Rhodococcus_phage	2.4e-31	33.4
WP_075267097.1|6471387_6471831_+	SRPBCC family protein	NA	NA	NA	NA
WP_075267098.1|6471883_6472579_-	nucleotidyltransferase	A0A1J0GW18	Streptomyces_phage	2.3e-14	36.0