CRISPRimmunity

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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_CP051462	Bacillus subtilis strain At3 chromosome, complete genome	3 crisprs	csa3,DEDDh,WYL,DinG,cas3	0	1	6	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP051462_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051462_1

968972-969079

Orphan

Consensus_repeat	Method
AAAACAAAACCAACAATCAGCTGCTGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051462_1

>merge|NZ_CP051462|1|968972-969079|CRISPRCasFinder
AAAACAAAACCAACAATCAGCTGCTGGTCAAGGTCAATTTGGCACTGAATTTGCTAGCGAAACAAACGCTCAGCAAGTCAAAAAACAAAACCAGCAATCAGCTGCTGG

>NZ_CP051462|1|1|968972-969079|CRISPRCasFinder
AAAACAAAACCAACAATCAGCTGCTGG	TCAAGGTCAATTTGGCACTGAATTTGCTAGCGAAACAAACGCTCAGCAAGTCAA
AAAACAAAACCAGCAATCAGCTGCTGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051462.1\|WP_084994288.1\|973474_974764_-\|glutamate-1-semialdehyde-2,1-aminomutase	unknown	unknown	gnl\|CDD\|183493
NZ_CP051462.1\|WP_019257848.1\|976555_977440_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379641
NZ_CP051462.1\|WP_003223257.1\|967797_968022_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP051462.1\|WP_003239685.1\|969758_970289_+\|DUF402-domain-containing-protein	unknown	unknown	gnl\|CDD\|184219
NZ_CP051462.1\|WP_084994300.1\|959827_960343_+\|SH3-domain-containing-protein	unknown	unknown	gnl\|CDD\|214600
NZ_CP051462.1\|WP_019257844.1\|972193_973255_-\|aromatic-acid-exporter-family-protein	unknown	unknown	gnl\|CDD\|226614
NZ_CP051462.1\|WP_168767771.1\|969354_969615_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|372951
NZ_CP051462.1\|WP_084994296.1\|960750_961611_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP051462.1\|WP_003239676.1\|974916_975390_+\|thioredoxin-dependent-thiol-peroxidase	unknown	unknown	gnl\|CDD\|224146
NZ_CP051462.1\|WP_014113119.1\|975994_976348_-\|YgzB-family-protein	unknown	unknown	gnl\|CDD\|371346
NZ_CP051462.1\|WP_003223285.1\|975522_975960_+\|peroxide-responsive-transcriptional-repressor-PerR	unknown	unknown	gnl\|CDD\|223806
NZ_CP051462.1\|WP_003239690.1\|968104_968857_+\|enoyl-[acyl-carrier-protein]-reductase-FabL	unknown	unknown	gnl\|CDD\|236145
NZ_CP051462.1\|WP_003239695.1\|965481_966465_-\|metal-dependent-hydrolase	unknown	unknown	gnl\|CDD\|224899
NZ_CP051462.1\|WP_003239683.1\|970375_972118_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP051462.1\|WP_084994292.1\|966681_967791_+\|A/G-specific-adenine-glycosylase	unknown	unknown	gnl\|CDD\|130156
NZ_CP051462.1\|WP_084994294.1\|962903_965489_+\|YfhO-family-protein	unknown	unknown	gnl\|CDD\|226888
NZ_CP051462.1\|WP_084994298.1\|960431_960764_+\|SdpI-family-protein	unknown	unknown	gnl\|CDD\|227945
NZ_CP051462.1\|WP_069149214.1\|985416_985974_+\|antiterminator-LoaP	unknown	unknown	gnl\|CDD\|193574
NZ_CP051462.1\|WP_003239709.1\|959413_959683_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379438
NZ_CP051462.1\|WP_003239699.1\|961842_962832_+\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|133030

Protein	Function_ID	Function_description	E-value
NZ_CP051462.1\|WP_084994288.1\|973474_974764_-\|glutamate-1-semialdehyde-2,1-aminomutase	gnl\|CDD\|183493	PRK12389, PRK12389, glutamate-1-semialdehyde aminotransferase; Provisional.	0
NZ_CP051462.1\|WP_019257848.1\|976555_977440_+\|hypothetical-protein	gnl\|CDD\|379641	pfam14540, NTF-like, Nucleotidyltransferase-like. Structural comparisons with Structure 1kny indicate that this N-terminal domain resembles a nucleotidyltransferase fold.	3.18717e-59
NZ_CP051462.1\|WP_014113119.1\|975994_976348_-\|YgzB-family-protein	gnl\|CDD\|371346	pfam11023, DUF2614, Zinc-ribbon containing domain. This is a family of proteins conserved in the Bacillaceae family. Some members are annotated as being protein YgzB. The function is not known.	1.8925e-70
NZ_CP051462.1\|WP_003239685.1\|969758_970289_+\|DUF402-domain-containing-protein	gnl\|CDD\|184219	PRK13662, PRK13662, hypothetical protein; Provisional.	1.54037e-126
NZ_CP051462.1\|WP_084994300.1\|959827_960343_+\|SH3-domain-containing-protein	gnl\|CDD\|214600	smart00287, SH3b, Bacterial SH3 domain homologues.	4.29507e-12
NZ_CP051462.1\|WP_019257844.1\|972193_973255_-\|aromatic-acid-exporter-family-protein	gnl\|CDD\|226614	COG4129, COG4129, Predicted membrane protein [Function unknown].	8.86488e-91
NZ_CP051462.1\|WP_168767771.1\|969354_969615_+\|hypothetical-protein	gnl\|CDD\|372951	pfam14182, YgaB, YgaB-like protein. The YgaB-like protein family includes the B. subtilis YgaB protein, which is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 90 amino acids in length.	4.93949e-25
NZ_CP051462.1\|WP_084994296.1\|960750_961611_+\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	2.2135e-38
NZ_CP051462.1\|WP_003239676.1\|974916_975390_+\|thioredoxin-dependent-thiol-peroxidase	gnl\|CDD\|224146	COG1225, Bcp, Peroxiredoxin [Posttranslational modification, protein turnover, chaperones].	3.57002e-86
NZ_CP051462.1\|WP_003223285.1\|975522_975960_+\|peroxide-responsive-transcriptional-repressor-PerR	gnl\|CDD\|223806	COG0735, Fur, Fe2+/Zn2+ uptake regulation proteins [Inorganic ion transport and metabolism].	2.19115e-56
NZ_CP051462.1\|WP_003239690.1\|968104_968857_+\|enoyl-[acyl-carrier-protein]-reductase-FabL	gnl\|CDD\|236145	PRK08063, PRK08063, enoyl-[acyl-carrier-protein] reductase FabL.	1.24786e-171
NZ_CP051462.1\|WP_003239695.1\|965481_966465_-\|metal-dependent-hydrolase	gnl\|CDD\|224899	COG1988, COG1988, Predicted membrane-bound metal-dependent hydrolases [General function prediction only].	2.15201e-44
NZ_CP051462.1\|WP_003239683.1\|970375_972118_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_CP051462.1\|WP_084994292.1\|966681_967791_+\|A/G-specific-adenine-glycosylase	gnl\|CDD\|130156	TIGR01084, A/G-specific_adenine_glycosylase, A/G-specific adenine glycosylase. This equivalog model identifies mutY members of the pfam00730 superfamily (HhH-GPD: Helix-hairpin-helix and Gly/Pro rich loop followed by a conserved aspartate). The major members of the superfamily are nth and mutY. [DNA metabolism, DNA replication, recombination, and repair].	2.2131e-154
NZ_CP051462.1\|WP_084994294.1\|962903_965489_+\|YfhO-family-protein	gnl\|CDD\|226888	COG4485, COG4485, Predicted membrane protein [Function unknown].	0
NZ_CP051462.1\|WP_084994298.1\|960431_960764_+\|SdpI-family-protein	gnl\|CDD\|227945	COG5658, COG5658, Predicted integral membrane protein [Function unknown].	1.03509e-21
NZ_CP051462.1\|WP_069149214.1\|985416_985974_+\|antiterminator-LoaP	gnl\|CDD\|193574	cd08000, NGN, N-Utilization Substance G (NusG) N-terminal (NGN) domain Superfamily. The N-Utilization Substance G (NusG) and its eukaryotic homolog Spt5 are involved in transcription elongation and termination. NusG contains an NGN domain at its N-terminus and Kyrpides Ouzounis and Woese (KOW) repeats at its C-terminus in bacteria and archaea. The eukaryotic ortholog, Spt5, is a large protein composed of an acidic N-terminus, an NGN domain, and multiple KOW motifs at its C-terminus. Spt5 forms a Spt4-Spt5 complex that is an essential RNA Polymerase II elongation factor. NusG was originally discovered as an N-dependent antitermination enhancing activity in Escherichia coli and has a variety of functions, such as being involved in RNA polymerase elongation and Rho-termination in bacteria. Orthologs of the NusG gene exist in all bacteria, but its functions and requirements are different. The diverse activities suggest that, after diverging from a common ancestor, NusG proteins became specialized in different bacteria.	1.67505e-23
NZ_CP051462.1\|WP_003239709.1\|959413_959683_+\|hypothetical-protein	gnl\|CDD\|379438	pfam14043, WVELL, WVELL protein. This family includes the B. subtilis YfjH protein, which is functionally uncharacterized. This is not a homolog of E. coli YfjH, a synonym for IscX, which belongs to pfam04384. This family of proteins is found in bacteria. Proteins in this family are approximately 90 amino acids in length and contain a highly conserved WVELL motif.	1.44803e-41
NZ_CP051462.1\|WP_003239699.1\|961842_962832_+\|glycosyltransferase-family-2-protein	gnl\|CDD\|133030	cd04187, DPM1_like_bac, Bacterial DPM1_like enzymes are related to eukaryotic DPM1. A family of bacterial enzymes related to eukaryotic DPM1; Although the mechanism of eukaryotic enzyme is well studied, the mechanism of the bacterial enzymes is not well understood. The eukaryotic DPM1 is the catalytic subunit of eukaryotic Dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. The enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. This protein family belongs to Glycosyltransferase 2 superfamily.	2.62301e-84

>NZ_CP051462.1|WP_003239690.1|968104_968857_+|enoyl-[acyl-carrier-protein]-reductase-FabL
MEQNKCALVTGSSRGVGKAAALRLAENGYNIVINYARSKKAALETAEEIEKLGVKVLVVKANVGQPAKIKEMFQQIEETFGRLDVFVNNAASGVLRPVMELEETHWDWTMNINAKALLFCAQEAAKLMEKNGGGHIVSISSLGSIRYLENYTTVGVSKAALEALTRYLAVELSPKQIIVNAVSGGAIDTDALKHFPNREDLLEDARQNTPAGRMVEIKDMVDTVEFLVSSKADMIRGQTIIVDGGRSLLV
>NZ_CP051462.1|WP_003223257.1|967797_968022_-|hypothetical-protein
MYVGRDMSELNMVSKEDWKNSELAYFHHAFQQIMPYLNEEGQSKYRELTQEIEARGGMKRNEADYSHGTRVSYD
>NZ_CP051462.1|WP_084994292.1|966681_967791_+|A/G-specific-adenine-glycosylase
MNVLEDKLKQKDIQQFRDDLISWFEREQRILPWREDQDPYKVWVSEVMLQQTRVETVIPYFLRFVEQFPTVEALADADEEKVLKAWEGLGYYSRVRNLQSAVKEVKQEYGGIVPPDEKEFGGLKGVGPYTKGAVLSIAYNKPIPAVDGNVMRVMSRILSIWDDIAKPKTRTMFEDAVRAFISKEKPSEFNQGLMELGALICTPKSPSCLLCPVQQHCSAFEEGTERELPVKSKKKKPGIKTMAAIVLTDDDGQVYIHKRPSKGLLANLWEFPNLETQKGIKTEREQLTAFLENEYGIQADISDLQGVVEHVFTHLVWNISVFFGKVKQVSDTSELKKVTKEELEQFAFPVSHQKIWKMAVEAAVYSAAP
>NZ_CP051462.1|WP_003239695.1|965481_966465_-|metal-dependent-hydrolase
MDTGTHVVMGIALGGIATLDPVVGADPAMAHAVMIATLAGSQAPDIDTVLKLKNNAVYIRNHRGFTHSIPAVLFWSVIIPAILYLFYPQADFLHLWLWTLLAVVLHVFVDIFNAYGTQAIRPFSKKWVALGLINTFDPFIFISHLAAIAIWYAGGSPGITFLSLYIILAGYYMVRLIMQLRIKRKLHEMIHDEIESIIISPTMKFRQWRIAVTTAHAFYVGRSMEGHVVILDTFNRVPVPETEVMQAAKQDDNIAAFLSFSPVYRWEVDTFKDHYEVRFIDLRYRSKGHYPFVAIVHIGHDLTIRSSYTGWIFSEEKLQKKLKLGSI
>NZ_CP051462.1|WP_084994294.1|962903_965489_+|YfhO-family-protein
MKRKYVMIYAASLLASVLAHAFFVKGWADGRYMTGPGDGLAQMIVFKKLLFEQYTHGNFFYNYSFGLGGGTFSQLGYYFSASFLFLAVSAAVWLLQAVQLIGEANTLFWAESAVFISIFKLSVIIFTAASVFHYILKHRAASFTGAVLYGVSIIYFRHEAYWEFFTDTMIWLPLLVLGAEKIIRERRPEWFIIACSLTLINNFYFAYINLIFIGIYVLFRWLIRLDEHEEKRWIQCRMFLVSGIISFGISAAAFVPVVYGFLNNLRPPYSQKIEWLNFDDNILFSSRIIILPAAFLLFLFIVSFYKNRVFRLFAGLSLLFILFHFSPYAASIFNGFSAPQNRFEYVLAFTIAGAAAAGLSQLSELKWKELLPAAAVVLLFYLYHIQRYELDIWKPANESILLLLFLTTAALFAAAFAKKRATVAVYGVIILSSLFVANTYQKYTLSEGGGLDSVTKAYLTGEEYKGQESSEIIRRLQKEDDDPLMRIDWMNGVRNNTPIIYGFNGFSAYSSILNKHLLTFYWNDLSIDMGRESVSRYASLGDRANLYSLLYGKYYMTEKTNEANVPYGFKKHLESEHYVVYENQYMLPFIKTADAIYSESELDKLPALAKEQAMLKGIVVADPSEKTEQAPKLANLIPKSDISAKHAQYQNGLFTVTGENGGELIITPKEASSSPGDYYVSFYLKSKAKDKGFTLRVNDYVTTRKSNQSIYKTGVNDITIRVPKSGHISIKLPKGTYELRNIALYEENYQTLKSAALQNKSDKADNLKWDKNKLTFTYRLPKNQYIMLPIPYEKGWELKINGKTKTIEKADYAFIGFKAQKGDNHIELAYYPPYFKISALISLVGLLLAVLYIRRKKPGSK
>NZ_CP051462.1|WP_003239699.1|961842_962832_+|glycosyltransferase-family-2-protein
MKQGLISIIIPSYNEGYNVKLIHESLKKEFKSIHYDYEIFFINDGSVDDTLQQIKDLAAVCSRVKYISFSRNFGKEAAILAGFEHVQGEAVIVMDADLQHPTYLLKDFIKGYEEGYDQVIAQRNRKGDSPVRSLLSSLYYKFINKAVEVDLRDGVGDFRLLSRQAVNALLKLSEGNRFSKGLFCWIGFDQKIVFYENVERKNGTSKWSFSSLFNYGMDGVVSFNHKPLRICFYTGIFILLLSIIYIIATFVKILTNGISVPGYFTIISAVLFLGGVQLLSLGIIGEYIGRIYYETKKRPHYLIKEANIPNKDLPETNELKSVRRLTKMH
>NZ_CP051462.1|WP_084994296.1|960750_961611_+|alpha/beta-hydrolase
MDGVNCQFVKTNGITLHVAAAGPEDGPLIVLLHGFPEFWYGWKNQIKPLADAGYRVIAPDQRGYNLSDKPDGIDAYRIDTLRDDIIGLITQFTDEKAIVIGHDWGGAVAWHLASTRPEYVEKLIAINIPHPHIMKTVTPVYPPQWLKSSYIAFFQLPDIPEASLKENDYETLDKAIGLSFRPELFSSDDVSRYKEAWKQPGALTAMLNWYRALRKGSLSEKTTCETVPYRMIWGMEDRFLSKKLAKETERHCPNGHLIFVDEASHWINHEKPAIVNILILEYLKKQ
>NZ_CP051462.1|WP_084994298.1|960431_960764_+|SdpI-family-protein
MAGLISGGLMVIAGILIKLFPPKSINSVYGYRTRRSMTDQRLWNEANRYSASLMIMSGLVIAALGLLLRSNLIILQLILLLAACVITFMLTEKRLKNMTHSQGGDMSGRS
>NZ_CP051462.1|WP_084994300.1|959827_960343_+|SH3-domain-containing-protein
MKKNQVLLALTAAAGLGLTATYSAPAAKAAPLHDISVSMPSSDSYIIKAGKLNVRTEPNHKGDILGTISSEQKVTVNGFANADWAQIQFKGKKAYISTHFLMKTASQAKTAKQTAFYAPTPENGKAKQLSSGTEVTILGWGFSENGGFDFTWAFVDYGGVKGYIHTKDLQI
>NZ_CP051462.1|WP_003239709.1|959413_959683_+|hypothetical-protein
MNTYIEKLTNLLLEKNDMISYIQAKTWVELLWSDFEATYAKAGHAYQGEKMTEKIVTQWIENYGGQLHLFQSSRDDVNDYLNQSRGLLH
>NZ_CP051462.1|WP_168767771.1|969354_969615_+|hypothetical-protein
MTEFEKLVSEQMKTMDKLLDLQSELDRCKQIEAELRHLERDARLLGIQNEIAVKQKHLADIQDMFQKQTEQVIRSYRSSEKPSSFV
>NZ_CP051462.1|WP_003239685.1|969758_970289_+|DUF402-domain-containing-protein
MGYPKEGETIQIHSYKHNGLIHRIWNETTILKSTEMCVIGANDRTMVTESDGRTWITREPAICYFHARQWFNVIGMLREDGVHYYCNISSPFAYDGEAIKYIDYDLDVKVFPDMTYNILDEDEYDDHRKSMNYPKEIDSILRDYLNTLLHWIHQRQGPFAPEFVDMWYERYLRYTK
>NZ_CP051462.1|WP_003239683.1|970375_972118_+|ABC-transporter-ATP-binding-protein
MGVMKRYMQFVKPYKKQIFVTVLIGIVKFSIPLALPLLLKYVVDDIIQGGGTANDKTTSLFTIMAIMFALFLILRPPVEYYRQYFAQWTASKVLYDIRAKLFDHIQKLSLRFYANTRTGEVISRVINDVEQTKDFVITGLMNIWLDMLTILIVISIMLTLDIKLTLISIVLFPLYGISVKYFYGRLRRLTRERSQALAQVQGHLHERIQGMPVIRSFAIEDHEQAHFNEKNSHFLDKAIRHTNWNAKTFAVVNTITDLAPLIVIACAGYFVINGPLTVGTMVAFVGYIDRMYNPVRRLINSSTTLTQSIASMDRVFEFIDEPYELTDKPNAIKADQIRGEVEFQNVSFQYEKEKENILHDVSLKVNKGETVALVGMSGGGKSTLVSLIPRFYDVTTGRLLIDGTDIRDYEARSLRNQVGMVLQDTFLFSETIRENIAIGKPDATLEEIIEAAKAANAHEFIMGFPEGYETRVGERGVKLSGGQKQRISIARVFLKNPPLLILDEATSALDLESEHYIQEAMDKLAKDRTTFVVAHRLSTITHADKIVVMENGTIIEVGTHDELMDYDSQYKHLFTIQNLS
>NZ_CP051462.1|WP_019257844.1|972193_973255_-|aromatic-acid-exporter-family-protein
MKLGARIFKTGIAITLALYLASWIGLPAPIFAGIAAIFAIQPSIYRSFLIIIDQVQANIIGAVIATVFGLIFGPSPIMIGLTAVIVITIMLKLKIEHTISIALVTVIAILESAGDDFLMFALVRTSTVILGVLSSFIVNLVFLPPKYETKLIHNTVENTEEIMKWIRLSMRQSTEHSILKEDIEKLKEKMIKLDQTYLLYKEERSYFKKTTYVKSRKLVLFRQAIITANRALDTLKKLHRLENDIYHMPEEFQETLTEELDYLLYWHELILMRFVGKIKPHDDADEEGIRYKQLLTKSFLKNQQNTDDELIDYNMLNIMASAVEYREQLEHLETLITSFQTYHPKDCEIETEE
>NZ_CP051462.1|WP_084994288.1|973474_974764_-|glutamate-1-semialdehyde-2,1-aminomutase
MHTKSIELHNEALEHIVGGVNSPSRSYKAVGGGSPVAMEKANGAYFWDVDGNKYIDYLAAYGPIITGHAHPHITEAIKKAAENGVLYGTPTKHEVTFAKMLKEAIPAMDKVRFVNSGTEAVMTTIRVARAYTGRTKIIKFAGCYHGHSDLVLVAAGSGPSTLGTPDSAGVPKSIANEVITVPFNDIESYKAALDKWGSEIAAVLVEPIVGNFGIVEPKEGFLEKVNELTHNAGALVIYDEVITAFRFMYGGAQDLLQMKPDLTALGKIIGGGLPIGAYGGKKEIMEQVAPLGPAYQAGTMAGNPASILSGIACLEVLKEECVYEKLDHLGAMLEEGILQHAETHGITITVNRLKGALTVYFSDEKVENYEQAERSDGETFAKFFKLMLERGINLAPSKYEAWFITTAHTEQDIKDTLVAVEDAFKHLKN
>NZ_CP051462.1|WP_003239676.1|974916_975390_+|thioredoxin-dependent-thiol-peroxidase
MTIEIGQKAPDLELKGDHGETVTLSDYKGKYIVLYFYPKDMTPGCTTEACDFRDSHESFAELDAVIIGVSPDSQEKHGKFKEKHNLPFLLLVDDEHKLAEAFDVWKLKKNFGKEYMGIERSTFLIDKEGRLVKEWRKVRVKDHVAEALQTLKDMSEK
>NZ_CP051462.1|WP_003223285.1|975522_975960_+|peroxide-responsive-transcriptional-repressor-PerR
MAAHELKEALETLKETGVRITPQRHAILEYLVNSMAHPTADDIYKALEGKFPNMSVATVYNNLRVFRESGLVKELTYGDASSRFDFVTSDHYHAICENCGKIVDFHYPGLDEVEQLAAHVTGFKVSHHRLEIYGVCQECSKKENH
>NZ_CP051462.1|WP_014113119.1|975994_976348_-|YgzB-family-protein
MAKYSSKINKIRTFALSLVFVGFIIMYIGIFFKESVLLSSLFMILGLLSIGLSTVVYFWIGMLSTKAVRVICPGCEKETKVLGRVDMCMHCREPLTLDKGLEGKEFDESYNKKKMSK
>NZ_CP051462.1|WP_019257848.1|976555_977440_+|hypothetical-protein
MDNLLRPIYQERASHPNTLAVIMIERRNKTSSLTDNFDAALLVIVKEADEPVFIKHYEFDQKTASLHVVTDSQIQEWILLGTNRRIIDWIVNGRVMFDRNEYIAELIDRLNTFPFAERKLKIGLEYGKLIRRYVEGKAFFEANQFLDAYNAVVHALHHLARIEVIDRGFHPETTVWSQVRQMEPQVYKLYSELIESHESLEKRLELLFLANDFLIHSKAEIGSAHLFEVMKGKDIWQFGELLQHPDLKHYTQDLGVMLDYLTEKGLINVCQIETKGQAVYHRGYFFKKDVDSDS
>NZ_CP051462.1|WP_069149214.1|985416_985974_+|antiterminator-LoaP
MSWYVLYVETGQEEIVKCLIKKYFADLTIEVIVPKRKIREKRQGKLYEVSRLLFPGYVFLNTYMNIDIYYGLKKIPRCFRLLNSYKYKTDYLVDDVSHNITSVFCTIEQKEIAPILQLLQQNETIGFSQIYKEDSEITVISGPLKGLEGIIKKIDKRKNRAKIELNFMGVIKLVDVGVEVLTRDS

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Crispr_ID: NZ_CP051462_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051462_2

1013185-1013292

Orphan

Consensus_repeat	Method
CCAGCAGCTGATTGCTGGTTTTGTTTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051462_2

>merge|NZ_CP051462|2|1013185-1013292|CRISPRCasFinder
CCAGCAGCTGATTGCTGGTTTTGTTTTTTGACTTGCTGAGCGTTTGTTTCGCTAGCAAATTCAGTGCCAAATTGACCTTGACCAGCAGCTGATTGTTGGTTTTGTTTT

>NZ_CP051462|2|2|1013185-1013292|CRISPRCasFinder
CCAGCAGCTGATTGCTGGTTTTGTTTT	TTGACTTGCTGAGCGTTTGTTTCGCTAGCAAATTCAGTGCCAAATTGACCTTGA
CCAGCAGCTGATTGTTGGTTTTGTTTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051462.1\|WP_168767771.1\|1012646_1012907_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|372951
NZ_CP051462.1\|WP_019713701.1\|995781_996738_-\|acyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|214838
NZ_CP051462.1\|WP_168767775.1\|1031090_1046273_+\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|225858
NZ_CP051462.1\|WP_168767774.1\|1016289_1031073_+\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|225858
NZ_CP051462.1\|WP_084993610.1\|1058571_1059789_+\|polyketide-beta-ketoacyl:ACP-synthase	unknown	unknown	gnl\|CDD\|180839
NZ_CP051462.1\|WP_168767778.1\|1064459_1065302_+\|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl\|CDD\|224007
NZ_CP051462.1\|WP_003239676.1\|1006872_1007346_-\|thioredoxin-dependent-thiol-peroxidase	unknown	unknown	gnl\|CDD\|224146
NZ_CP051462.1\|WP_019713718.1\|1061854_1062604_+\|PRK07110-family-protein	unknown	unknown	gnl\|CDD\|235936
NZ_CP051462.1\|WP_003223285.1\|1006302_1006740_-\|peroxide-responsive-transcriptional-repressor-PerR	unknown	unknown	gnl\|CDD\|223806
NZ_CP051462.1\|WP_168767777.1\|1062622_1064434_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235936
NZ_CP051462.1\|WP_019257844.1\|1009006_1010068_+\|aromatic-acid-exporter-family-protein	unknown	unknown	gnl\|CDD\|226614
NZ_CP051462.1\|WP_069149214.1\|996888_997446_-\|antiterminator-LoaP	unknown	unknown	gnl\|CDD\|193574
NZ_CP051462.1\|WP_168767776.1\|1050601_1058575_+\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|238429
NZ_CP051462.1\|WP_003239685.1\|1011972_1012503_-\|DUF402-domain-containing-protein	unknown	unknown	gnl\|CDD\|184219
NZ_CP051462.1\|WP_084994511.1\|1046269_1050376_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225858
NZ_CP051462.1\|WP_168767773.1\|1013537_1016276_+\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP051462.1\|WP_084993614.1\|1061067_1061829_+\|enoyl-CoA-hydratase/isomerase	unknown	unknown	gnl\|CDD\|235938
NZ_CP051462.1\|WP_019257848.1\|1004822_1005707_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379641
NZ_CP051462.1\|WP_003239683.1\|1010143_1011886_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP051462.1\|WP_014113119.1\|1005914_1006268_+\|YgzB-family-protein	unknown	unknown	gnl\|CDD\|371346

Protein	Function_ID	Function_description	E-value
NZ_CP051462.1\|WP_168767771.1\|1012646_1012907_-\|hypothetical-protein	gnl\|CDD\|372951	pfam14182, YgaB, YgaB-like protein. The YgaB-like protein family includes the B. subtilis YgaB protein, which is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 90 amino acids in length.	4.93949e-25
NZ_CP051462.1\|WP_019713701.1\|995781_996738_-\|acyltransferase-domain-containing-protein	gnl\|CDD\|214838	smart00827, PKS_AT, Acyl transferase domain in polyketide synthase (PKS) enzymes.	7.2773e-69
NZ_CP051462.1\|WP_168767775.1\|1031090_1046273_+\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051462.1\|WP_168767774.1\|1016289_1031073_+\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051462.1\|WP_084993610.1\|1058571_1059789_+\|polyketide-beta-ketoacyl:ACP-synthase	gnl\|CDD\|180839	PRK07103, PRK07103, polyketide beta-ketoacyl:acyl carrier protein synthase; Validated.	0
NZ_CP051462.1\|WP_168767778.1\|1064459_1065302_+\|sugar-phosphate-isomerase/epimerase	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	1.16405e-35
NZ_CP051462.1\|WP_003239676.1\|1006872_1007346_-\|thioredoxin-dependent-thiol-peroxidase	gnl\|CDD\|224146	COG1225, Bcp, Peroxiredoxin [Posttranslational modification, protein turnover, chaperones].	3.57002e-86
NZ_CP051462.1\|WP_019713718.1\|1061854_1062604_+\|PRK07110-family-protein	gnl\|CDD\|235936	PRK07110, PRK07110, polyketide biosynthesis enoyl-CoA hydratase; Validated.	6.36607e-150
NZ_CP051462.1\|WP_003223285.1\|1006302_1006740_-\|peroxide-responsive-transcriptional-repressor-PerR	gnl\|CDD\|223806	COG0735, Fur, Fe2+/Zn2+ uptake regulation proteins [Inorganic ion transport and metabolism].	2.19115e-56
NZ_CP051462.1\|WP_168767777.1\|1062622_1064434_+\|hypothetical-protein	gnl\|CDD\|235936	PRK07110, PRK07110, polyketide biosynthesis enoyl-CoA hydratase; Validated.	1.08693e-117
NZ_CP051462.1\|WP_019257844.1\|1009006_1010068_+\|aromatic-acid-exporter-family-protein	gnl\|CDD\|226614	COG4129, COG4129, Predicted membrane protein [Function unknown].	8.86488e-91
NZ_CP051462.1\|WP_069149214.1\|996888_997446_-\|antiterminator-LoaP	gnl\|CDD\|193574	cd08000, NGN, N-Utilization Substance G (NusG) N-terminal (NGN) domain Superfamily. The N-Utilization Substance G (NusG) and its eukaryotic homolog Spt5 are involved in transcription elongation and termination. NusG contains an NGN domain at its N-terminus and Kyrpides Ouzounis and Woese (KOW) repeats at its C-terminus in bacteria and archaea. The eukaryotic ortholog, Spt5, is a large protein composed of an acidic N-terminus, an NGN domain, and multiple KOW motifs at its C-terminus. Spt5 forms a Spt4-Spt5 complex that is an essential RNA Polymerase II elongation factor. NusG was originally discovered as an N-dependent antitermination enhancing activity in Escherichia coli and has a variety of functions, such as being involved in RNA polymerase elongation and Rho-termination in bacteria. Orthologs of the NusG gene exist in all bacteria, but its functions and requirements are different. The diverse activities suggest that, after diverging from a common ancestor, NusG proteins became specialized in different bacteria.	1.67505e-23
NZ_CP051462.1\|WP_168767776.1\|1050601_1058575_+\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|238429	cd00833, PKS, polyketide synthases (PKSs) polymerize simple fatty acids into a large variety of different products, called polyketides, by successive decarboxylating Claisen condensations. PKSs can be divided into 2 groups, modular type I PKSs consisting of one or more large multifunctional proteins and iterative type II PKSs, complexes of several monofunctional subunits.	0
NZ_CP051462.1\|WP_003239685.1\|1011972_1012503_-\|DUF402-domain-containing-protein	gnl\|CDD\|184219	PRK13662, PRK13662, hypothetical protein; Provisional.	1.54037e-126
NZ_CP051462.1\|WP_084994511.1\|1046269_1050376_+\|hypothetical-protein	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051462.1\|WP_168767773.1\|1013537_1016276_+\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP051462.1\|WP_084993614.1\|1061067_1061829_+\|enoyl-CoA-hydratase/isomerase	gnl\|CDD\|235938	PRK07112, PRK07112, enoyl-CoA hydratase/isomerase.	1.80743e-150
NZ_CP051462.1\|WP_019257848.1\|1004822_1005707_-\|hypothetical-protein	gnl\|CDD\|379641	pfam14540, NTF-like, Nucleotidyltransferase-like. Structural comparisons with Structure 1kny indicate that this N-terminal domain resembles a nucleotidyltransferase fold.	3.18717e-59
NZ_CP051462.1\|WP_003239683.1\|1010143_1011886_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	0
NZ_CP051462.1\|WP_014113119.1\|1005914_1006268_+\|YgzB-family-protein	gnl\|CDD\|371346	pfam11023, DUF2614, Zinc-ribbon containing domain. This is a family of proteins conserved in the Bacillaceae family. Some members are annotated as being protein YgzB. The function is not known.	1.8925e-70

>NZ_CP051462.1|WP_168767771.1|1012646_1012907_-|hypothetical-protein
MTEFEKLVSEQMKTMDKLLDLQSELDRCKQIEAELRHLERDARLLGIQNEIAVKQKHLADIQDMFQKQTEQVIRSYRSSEKPSSFV
>NZ_CP051462.1|WP_003239685.1|1011972_1012503_-|DUF402-domain-containing-protein
MGYPKEGETIQIHSYKHNGLIHRIWNETTILKSTEMCVIGANDRTMVTESDGRTWITREPAICYFHARQWFNVIGMLREDGVHYYCNISSPFAYDGEAIKYIDYDLDVKVFPDMTYNILDEDEYDDHRKSMNYPKEIDSILRDYLNTLLHWIHQRQGPFAPEFVDMWYERYLRYTK
>NZ_CP051462.1|WP_003239683.1|1010143_1011886_-|ABC-transporter-ATP-binding-protein
MGVMKRYMQFVKPYKKQIFVTVLIGIVKFSIPLALPLLLKYVVDDIIQGGGTANDKTTSLFTIMAIMFALFLILRPPVEYYRQYFAQWTASKVLYDIRAKLFDHIQKLSLRFYANTRTGEVISRVINDVEQTKDFVITGLMNIWLDMLTILIVISIMLTLDIKLTLISIVLFPLYGISVKYFYGRLRRLTRERSQALAQVQGHLHERIQGMPVIRSFAIEDHEQAHFNEKNSHFLDKAIRHTNWNAKTFAVVNTITDLAPLIVIACAGYFVINGPLTVGTMVAFVGYIDRMYNPVRRLINSSTTLTQSIASMDRVFEFIDEPYELTDKPNAIKADQIRGEVEFQNVSFQYEKEKENILHDVSLKVNKGETVALVGMSGGGKSTLVSLIPRFYDVTTGRLLIDGTDIRDYEARSLRNQVGMVLQDTFLFSETIRENIAIGKPDATLEEIIEAAKAANAHEFIMGFPEGYETRVGERGVKLSGGQKQRISIARVFLKNPPLLILDEATSALDLESEHYIQEAMDKLAKDRTTFVVAHRLSTITHADKIVVMENGTIIEVGTHDELMDYDSQYKHLFTIQNLS
>NZ_CP051462.1|WP_019257844.1|1009006_1010068_+|aromatic-acid-exporter-family-protein
MKLGARIFKTGIAITLALYLASWIGLPAPIFAGIAAIFAIQPSIYRSFLIIIDQVQANIIGAVIATVFGLIFGPSPIMIGLTAVIVITIMLKLKIEHTISIALVTVIAILESAGDDFLMFALVRTSTVILGVLSSFIVNLVFLPPKYETKLIHNTVENTEEIMKWIRLSMRQSTEHSILKEDIEKLKEKMIKLDQTYLLYKEERSYFKKTTYVKSRKLVLFRQAIITANRALDTLKKLHRLENDIYHMPEEFQETLTEELDYLLYWHELILMRFVGKIKPHDDADEEGIRYKQLLTKSFLKNQQNTDDELIDYNMLNIMASAVEYREQLEHLETLITSFQTYHPKDCEIETEE
>NZ_CP051462.1|WP_003239676.1|1006872_1007346_-|thioredoxin-dependent-thiol-peroxidase
MTIEIGQKAPDLELKGDHGETVTLSDYKGKYIVLYFYPKDMTPGCTTEACDFRDSHESFAELDAVIIGVSPDSQEKHGKFKEKHNLPFLLLVDDEHKLAEAFDVWKLKKNFGKEYMGIERSTFLIDKEGRLVKEWRKVRVKDHVAEALQTLKDMSEK
>NZ_CP051462.1|WP_003223285.1|1006302_1006740_-|peroxide-responsive-transcriptional-repressor-PerR
MAAHELKEALETLKETGVRITPQRHAILEYLVNSMAHPTADDIYKALEGKFPNMSVATVYNNLRVFRESGLVKELTYGDASSRFDFVTSDHYHAICENCGKIVDFHYPGLDEVEQLAAHVTGFKVSHHRLEIYGVCQECSKKENH
>NZ_CP051462.1|WP_014113119.1|1005914_1006268_+|YgzB-family-protein
MAKYSSKINKIRTFALSLVFVGFIIMYIGIFFKESVLLSSLFMILGLLSIGLSTVVYFWIGMLSTKAVRVICPGCEKETKVLGRVDMCMHCREPLTLDKGLEGKEFDESYNKKKMSK
>NZ_CP051462.1|WP_019257848.1|1004822_1005707_-|hypothetical-protein
MDNLLRPIYQERASHPNTLAVIMIERRNKTSSLTDNFDAALLVIVKEADEPVFIKHYEFDQKTASLHVVTDSQIQEWILLGTNRRIIDWIVNGRVMFDRNEYIAELIDRLNTFPFAERKLKIGLEYGKLIRRYVEGKAFFEANQFLDAYNAVVHALHHLARIEVIDRGFHPETTVWSQVRQMEPQVYKLYSELIESHESLEKRLELLFLANDFLIHSKAEIGSAHLFEVMKGKDIWQFGELLQHPDLKHYTQDLGVMLDYLTEKGLINVCQIETKGQAVYHRGYFFKKDVDSDS
>NZ_CP051462.1|WP_069149214.1|996888_997446_-|antiterminator-LoaP
MSWYVLYVETGQEEIVKCLIKKYFADLTIEVIVPKRKIREKRQGKLYEVSRLLFPGYVFLNTYMNIDIYYGLKKIPRCFRLLNSYKYKTDYLVDDVSHNITSVFCTIEQKEIAPILQLLQQNETIGFSQIYKEDSEITVISGPLKGLEGIIKKIDKRKNRAKIELNFMGVIKLVDVGVEVLTRDS
>NZ_CP051462.1|WP_019713701.1|995781_996738_-|acyltransferase-domain-containing-protein
MKEKIIFMFSGQGSQYFKMGKELYEYESIFSKNMGQLDAVFQKATGKSIINYIYNEHRLKSDIFSDLFYTHPAIFITEVALARLLVSKGIRPHAVIGSSMGEYAAAVVADVFQPEEVLNILIDQVQLLNKFSSPGGMMAILDTHKIYDEVPILHHHANLAAINNESHFVISANQEGIKTVERYLRLKEITYHKLPVTIPFHSEHIELASEAVQESLSQISFKSPCLPFYSSVTGKKLEHLTAEYFWNVLKKPIHFIRALTEAVDHGGTILIDLGPSGTLANLAKAHFRNRTDISIFSILSPYTDNVRALESVYTKSVQ
>NZ_CP051462.1|WP_168767773.1|1013537_1016276_+|type-I-polyketide-synthase
MTRILKQILSVREVFATRYPEADNLDAYWSNLKAGRDSIREIPPSRWDVASFYQPFPSDEGKIYSKWLGLMDDVACFDPLFFNIAPSEAETMDPQQRLFLQEGYQAFADAGYTPEALNGQNCGVYLGIMANEYYRMLCEQQYGLTDMTGNYASIASARIAYFLNLKGPALSIDTACSSSLVAINLACEALLNRKIDMALAGGVTLYLTPKPYIEMCAAHMLSPEGRCKAFDKSSDGMVPGEGVGAVVLKRLQDAEADNDLIYGVIIGFGINQDGKTNGLTAPSVKSQIALERSIYQKYNIDPSSISYAEMHGTGTQLGDPIELKALSTAFQEKTDKKQFCAIGSVKSNIGHTSAAAGVASVHKVLLSMQHQQLVPTLHFKEPNEYFDFKNSPFYVNTQTRPWDANSPRRACVSSFGFSGTNAHLVIEAYDTKKKRVRMPVTDASRPALFVLSAKTEKQLKVYAGIMKEWIASQVDVNLKDMTYTLQTSREAMDYRMAFWMDSKFAAIDMLTAYLNDEQPDGLHISHVKKRKVQRNTSLHTDPETLFSQWLAGEWVDWQVFYKDDEPRHIRLPGYPFAKEHYWLPKQDTTSSSNSTLHPLVHLNTSDLSTQRFTTILTGKEAYLTDHQVKERRVLPGSAYLEMARTALEQGVDRVTTDTLQHGTAFICLQEHIWIAPLVVEDKPVEVHITLALIENGNVEYEIYSGSDHPDDQSAVLHAQGVLKVSELTPPKRQSLQQLKSQYPWHTLLPENIYPLFREAGLYYGPSHSGIERLYLHKDQILAKISILPESRGDRECYLDPGLLDAVFQATAGFAISLNAPLDSLPFTLKEMYIYQPCPKQVWAYIRQREKGRVFDIDVYDENGMVCVRILGFETRRGAGLMSEEAFYRHLSERIWNGELSQEEVERILMASR
>NZ_CP051462.1|WP_168767774.1|1016289_1031073_+|SDR-family-NAD(P)-dependent-oxidoreductase
MDGQWKHIYRQLKEKEITPEEASWQFKQWGKHKEKDHAANDLLPALKEIAAEVLAIDANEIHHDVLLGEQGFDPLKLNQLANRLNTKFGLELTTKDLAEQNTLDDLAQFLQAAKPSQGDQRLREKTINYLKEHLSSVFKINAEEIASDIDLEKYGINSIMVLKLTQQLEGFFGSLPKTLFFEYKTVDELTGYFLQHHREALTKVLGDSQPAPVSQPVGTEKRHKHSRRRRKEFRKAPSFSSSSSTPDIAIVGLAGRYPGARNMQEFWANLKGGKDCITPVPEERLALWQTPQKGEMWGGFLQDVDRFDPLFFHISPREAERMDPQERLFLECVYETLQDAGYTRQSLGAIQGQGMAGNVGVFVGVMYEEYQLYGAQEQLKGRPVAVNGNAASIANRVSYFCNFHGPSMAVDTMCSSSLTAIHLACQHLQRGSCEAAIAGGVNISIHPNKYVALNQGEFLSSKGRCESFGEGGDGYVPGEGVGAVLLKPLTQAVADGDHIYGVIKGTAINHGGKTHGYTVPNPTAQTDVIQRALQQAKVDPRTIDYIEAHGTGTALGDPIEIAGLTKAFEAYTQDRQFCAIGSVKSNIGHAESAAGIAGITKILLQMKYGQLVPSLHSKVLNTHIDFASTPFAVQQTLAEWERPPEGPRRAGISSFGAGGANAHVVIEEYIPEAAQETIAVSPGPYLIVLSAQSEGQLLEQAKRLLSAVTEAGWTDRDLADIAYTLQIGREAMDERLAVVVTSIADLKAKLTDIIAQTPDMADYYRGEVKAHKAAMAVLVDEDMAVTLEAWQQKGKYDKLLKLWVKGMAVDWERLYSETKPQRISLPTYPFTRDRYWIPVEEPKGQGITEAFHPLLHQNTSDFYEQRFSTRFTGEEPFLSDHVVVGQRMLPGSAYLEMARAAVSQAVGGWLGEGEGIRLQQVGWVRPLIVGDKPVEIHMGLAVEKDEAIRFDVYRETDEGEEVVYSEGRAELLTEKAPPLVDLSRIQQACGQKELSREAVYTAFANMGIQYGESHRGIERIYVGQEEVLARLTLASPWVHGGLHPGMVDAAIQAGIGLQEGFDQRQPSVPFAMEEVAIYRETQEAMWAWVRREDGQVTIVLCDDEGQICLEIKGLAVRVMELAGMEESIDHLLLHPHWQEQPVKATSANFDDHKVILCGMADLSPDHLHGFLEGEQCQVLQRVKGHQGECFQQYALQLFEALQHMMKAGHKKQVLVQVVIPLQEEELYEGLWAILQTAHLENPHMIGQLIAVDAGESAKAVAEKLKENAASSLPGHIRYQNGRRNIARWKILEAPPSHAALPWKKEGVYLITGGLGGLGLLFAKEIAKHAPQSTLILTGRSPLDQKKEADIQALTAMDIQVVYHQIDVTDRLAVKHLVDDTLKVYGQLHGVIHSAGIIRDNFIIKKSASQFHEVMAPKTLGLVNLDLACQACPLDFFIIFSSLAGGIGNVGQADYAGASAFMDAYARYRHRLVVAKKRHGRTISFNWPLWQDGGMHLDTETEAIMRKSTGMVAMETSRGMAAFYEGLASPYAQVMVIAGERGRFQEIHSRLHIQPAPKAEHTSVITAGPGQEGLRGKATDYIKRLLSVVLKLPADQIEADADFMTYGMDSVMVLKLTQQLEGFFGSLPKTLFFEYKTVDELTGYFLQHHREALTKVLGDSQPAPVSQPVGTEKRHKHSRRRRKEFRKAPSFSSSSSTPDIAIVGLAGRYPGARNMQEFWANLKGGKDCITPVPEERLALWQTPQKGEMWGGFLQDVDRFDPLFFHISPREAERMDPQERLFLECVYETLQDAGYTRQSLGAIQGQGMAGNVGVFVGVMYEEYQLYGAQEQLKGRPVAVNGNAASIANRVSYFCNFHGPSMAVDTMCSSSLTAIHLACQHLQRGSCEAAIAGGVNISIHPNKYVALNQGEFLSSKGRCESFGEGGDGYVPGEGVGAVLLKPLTQAVADGDHIYGVIKGTAINHGGKTHGYTVPNPTAQTDVIQRALQQAKVDPRTIDYIEAHGTGTALGDPIEIAGLTKAFETYTQDRQFCAIGSVKSNIGHAESAAGIAGITKILLQMKYGQLVPSLHSKVLNTHIDFASTPFAVQQTLAEWERPPEGPRRAGISSFGAGGANAHVVIEEYIPEAAQETIAVSPGPYLIVLSAQSEGQLLEQAKRLLSAVTEAGWTDRDLADIAYTLQIGREAMDERLAVVVTSIADLKAKLTDIIAQTPDMADYYRGEVKAHKAAMAVLVDEDMAVTLEAWQQKGKYDKLLKLWVKGMAVDWERLYSETKPQRISLPTYPFTRDRYWIPVEEPKGQGITEAFHPLLHQNTSDFYEQRFSTRFTGEEPFLSDHVVVGQRMLPGSAYLEMARAAVSQAVGGWLGEGEGIRLQQVGWVRPLIVGDKPVEIHMGLAVEKDEAIRFDVYRETDEGEEVVYSEGRAELLTEKAPPLVDLSRIQQACGQKELSREAVYTAFANMGIQYGESHRGIERIYVGQEEVLARLTLASPWVHGGLHPGMVDAAIQAGIGLQEGFDQRQPSVPFAMEEVAIYRETQEAMWAWVRREDGQVTIVLCDDVGRICLEMKGLATRIMNQEIETNAPTGYRMLAPVWERIRHTNDQKTVSSSHPVVFTGKKADGKTAIISQQYPKARVLHIDAGTTIEGIIAKFKSIEEMDELIWYMPELPVSSVADEGLIAAQEQTVIALFRVVKALLRLGYGQNALQWTIVTGRAQQVHPQEAIQPAQSALYGFAGSLAKEYPRWQIRLLDLNEGDDLQPLTQIHHLPEKMLAFREGSWYHQRLVQVEQTAELQMPYKKGGVYVVIGGAGGLGEVWSEHVIRHYQAKVVWIGRREKDEVIRSKISRLAALGPAPDYIAADAANRQSLEEAYQQIKEKYGEIQGVIHSAIVLRDQRIAQMDEETFRAALTAKVNVSVRIAQVFADESLDFVLFFSSIQSFATSAGQSNYAAGCTFKDAFALAMEREWTCPVKIMNWGYWGSVGVVAEEIYQQKMAQAGIGSIEGPEGMAAVDFLLSQPCPQLAYINTLRPLHEQEIGLSETIAIYPEEINTCMANLIQEQPAEEDTAEQAILAITQRMEQGQPLLVKLLWGQLQKAGLFQNKQGSLTELTLGLQPNYRRWMKETATIFEEHKYLSWDGQAYSVLEDPVDNMAIWQEWEQFKQTWEDEKGMQSHLTLIEATLRKLPDILTGQVTATDILFPNSSIELVEGIYKQNAVADYYNQRLASILVNYLQQRQRHQKPVRILEIGAGTGGSTAEVLKRIQPYHDSIDEYTYTDISKSFLLFAEKYFGDWKNRITYRMFDVTKPVVEQGIDPGGYDVVIASNVLHATPVLRETLRNTKALLKKNGLLLLIETTTHTLFNHLTFGLLDGWWLYEDEAWRIPGSPLVTVDQWERVLASEGFLTMVVPNANGQQHIILAESNGVIRQKKPTDEHPQKVEQSQQVEKPVPIVAAQPIRLGESLHTACVDYMKHLAGDILRLSAEQIDSAEPLERYGFDSILVTQMTSLLRKDFADISSTLLFEYQTLDDLADYLIKNHYQRAKDLLTFNPETDDQPVSEAPPSRPVKKKFRRKARSLRSLVSHGSQTGSNLMDVAIIGIAGRYPKANNIHEYWQLLKSGQQAVTSIPKERWDWQQYYDEEPGKPGYMYTKWGGFINGIDQFDPYFFHLSPAEAKRMDPQERLFLETCYESIADAGYTPSNLSKDRKVGVFVGAMNGHYPPGASYWSIANRVSYILNFQGPSLAVDSACSSSLTAIHLALESLYSGTSTCAVAGGVNLIVHPDHFLKLSAMTMLSPGDTCRPFSQQADGIVDSEGIGAVVLKPLEQAEVDGDHIYGVIKGSTINAGGKTNGYTVPNPHSQAKLIIEALERTKLDARTISYIEAHGTGTALGDPIEIKGLTTAFEKYTHERQFCAIGSVKSNIGHSESAAGIAGLTKVLLQLKHHQLVPSLHAEELNTRIDFSQTPFAVQQKLADWKRPVIYKGGKMQEYPRRAGISSFGAGGANAHLLIEEYIPRNDQRASLSITPDQPAIIVLSAKTEEQLRQQAIQLLTSIKQQAFTDDHLADIAYTLQIGREVMEERLAITVSSIEALRQRLDAYIQQVEDPHRISGRCSSRDVTSVIPEKSIIQWIETGAYQPLMEAWVNGGAIDWHLLYQNGKPSRISLPAYPFARDRYWITEVKRDIYQDSAIHPLVHQNISDVKGLKFKTKLNEHAFYFQDHAIDSIGVLPGVAYLEMASTAAKAVMSEQGKTDVCLKNVIWSKPFKQQDAQSPLIIGIVPQHNQLMAFTIYQPIDGEETIYCEGEITLGAFTQAADGLDLSLLQEQCQQRVLTSEECYQAFRSMGIVYGPHFQGIEKIYVGQRQALAKIHLPVCTADKQDAYTLHPGLLDASIQSAVGLTLSDAGQGLALPFAMDELVLIGDCLKAEWAFVRQRDEGRGITKMDIDICDEQGDCVLLIKGLTLKSKPVQDAILFYPHWEEKVVAPSAPSFKEENGHVIIYGAEPKIAQKISDQLPDEVCHVIPYDGDHFDIAGQFVRDALQVFHIIQGILKAKPTHVVPVQILLFNQSDNPFGKALSGMLQTAHLENPHIIGQCIMLDGDMESDHVLTILHDNRQVMATPQVAYRGSQKRHALRWKEVPLSEKKESLLWKEGGVYLITGGNGGLAKIIIQEIALHIQRGVVILVGRSQPTKDMQQWLNEWQQSELKVIYRSLDVTDRQAVQRCIKDIKGTYGDLNGIIHGAGVTDDHFMIQKKATQFTQVLAPKVAGVVHLDEASQDCHLDFFVIFSSITGVMGNIGQADYATANAFVDQYAYYRNSLVKSQKRQGRTFSINWPLWEDGGMQVTSQQQRQWKNDTGMVALKPEAGIRAFYQAWASPWQQVMVLAGDRDKLCRFVGEQEEEQENDATFYLTLIEQIASNELSEKEFMQLLQSHHRQVKTL
>NZ_CP051462.1|WP_168767775.1|1031090_1046273_+|SDR-family-NAD(P)-dependent-oxidoreductase
MEHTVKSLYRKIKNKSISEEEAVKRMTKLFSSTPIAEPLKELQQILMDILNIDTVDISEDTEWLEFGLDQVSLKKFADCLYHHYHLELTPAQIMAQGSLKGLASYVTQHIDSVQKGHAFYRKTDQLGIIAVDYLKKRLSAVLEIPLERLAADAPLENYGIDSVMIMKLTRQLEEHFGPLSKTLFFEYQTIQELADYLVKAHSHTLIKLFGIEETVAARSYELQPSLPLKEREESENHQAENVLLAEEDGIAVIGLAGRYPGAHNIKQFWENLQAGKDSITEISPDRWDHRLYFDEDKHKPGKINSKWGGFIEGVDQFDPLFFNISPREAEVLDPQERLFLECVYETLEDAGYSREALRSTDAVGVFVGAMYEEYPLYGAEEQAKGNALALGSNLSAIANRVSYFFNLTGPSMVVNTMCSSSLTSLHLACQSILRGECELAIAGGVNLSIHPNKYLLLGQGNFASSNGRCQSFGEGGDGYVPGEGVGAVFLKPLAQAIRDQDHIYGVIKGTAVNHGGKTNGYTVPNPNAQAKVVERALAQANVHPRTITYLEAHGTGTALGDPIEITGLKKAFDVYTADRQFCSIGSVKSNIGHCEGAAGIAGLTKVLLQMKYKKRVPSLHTQVLNPHIDFDETPFKVQQILEGWERPVIDLEGEKKKYPRRAGISAFGAGGSNAHVVVEEYIQEKTMDHHGYPHPALIVLSAKDATALQQQVERLLEAIESDNDRDLMDVAYTLQVGREAMEERLALTADTMSKLKEKLKAFLDGKENNGVFHGTAQSGKAVLSTMSADDDMKTIIATWLQKGKYDQLLQLWVKGLHVDWNILYPNGTPYRISLPTYPFARQTCWFSGVEKIAEQPISTPSRKEASNQELQPPSVEGCMYLPVWEEAQAVPNEQPHHQQVVIVYEKSAASLKEAIINYYHTCSSMPRIIQVCLGTTTERRATDHWECDIHDDTAFDRSLADCGEIDGLYFLAEHALVYDSVHSQNIKQSQMRNEVPLLRLIKRLNDSQSTGKPIDCYILTLDNYSLSEQPVNPYGGGVTGLVYSAAQGEHRLRIRNLDLSFVDIQAPRADLIEKIVCEPPSHRGEVIKLKQGRRYHQVFYEMEDVTQQETGAIREKGVYVIVGGSGTIGQVITRYLMADFGAQVIWVGRTPEKDHAIQTKMAAFQGRSGSLSYIQADVTDEAQMKRAVQLIKEQYKVIHGAIFSGVVFSFENTIRQTTEAEFLDILNVKTVGGLSFYSALAGEDLDFMLYFSSGQAYAFSGASKFSAYAAGVTFADALVRSLKNRSSFPVGSINWGFWQSSVAGTFLEDRTSALEDKEGFDCFVHSVDLLTKGLLEQSLCLRPTPSLKEMMKVKSGRVTIYPPTTEPMLNVLSSQWSDRIYQGEPQEGNRLAAQMEARVANVLFVQLSRLGLPPKGTTVNITDIINNSDITEKYQRWLAECLRILADHGYIHYEADQVTTVADAKPVETIWQDWQTTVTEYANNQDWKVQTMLLDSCLRKLPDILTGRILATEVLFPNTSIQSVEGIYKGNSIADYFNLTLADVLEAYIQRRIAKHPRERIRIIEAGAGTGGTSAIVLKRIEAYSTHVDYVYTDISKSFLLFAEEQYGTTYPNLTFQTWNVEQSASAQGVAAGSYDILIASNVLHATQAIRHTLQQVKAVLKPNGLILLNEMTQKNLFATVTFGLLDGWWLFQDDQLRIEGSPLIAAPTWQRVMEEEGFRQVAFLGEQGPNNGQRIIVAESDGWVRLPVAQEEKYKEEPMVPMDHTVIPQAITKVNLSDKQIADYVKATMIEQLAIALKVSKDRISPDVAFSEYGVDSILGVAFVKQLNEVFNIDLNSAILFDYTSVHRLAEYIADVYQEHIVTQLQVGSSRQAQEKPTVPIQISSEKPKPEKDNTQAIAVVGMAGQFPDAPDLHSFWEHLKKGHDGVHELPANYLDQGKYYDKVKQPGKTYSKWGGILAEKNAFDPLFFNISPREAASMSPHQRLVLQESWKALEDAGYNPKNLAEAPVGVFIGAEPANYYHESFTGSSDAIVASRLSYFLNLMGPAMVVNTGCSSSAAAIHLACESLRRGETTLAIAGGVYAKLDTTSLVALSGIDMISPTGKCFTFDEKADGTVLSEGVGIVVLKPLHQAEADGDPIYGVIVGSGMNQDGASNGITAPNGLAQERLLMDVYKKYDIQPNDISYVEAHGTGTALGDPIEVNALIRTFKRFTSKEHYCAIGSTKSSIGHTGAAAGVIGLMRVLLSMAHRQIPRLINFNTLNPLIALQQSPFYINTETVDWVPPRDKPLLAAVNSFGHSGTNVHLVVQEYKPSEVKEYKDGSSMLIPLSARKKDRLQAYAEKLLAYLNKKEQEGQLQHLRLSSLAYTLQTGREAMAERVVFLVNDMSDLIRALSDFCAGKARASTWQGQQQKGASSAGLLERDDEDLKVAMMQLAAKGKLTKIAQAWAEGMDINWDVLYGYEKPLRIHLPVYPFAKKYYERWEDTEKTVEATQRTAIHPLLQENTSNLQGIQFRSTFAGSESFLKDHLVQKKRMMPGMAYLEMARAAVEKVAQSGEMTICLHKMVWLKPFFVEDEPQKMRVTLSVSQDGEIVYDMRHDTSNDVVYHRGRAVFHKAEEPPTLDIPALIKACNRKILSRNEAYKAYQEAGLMYGPSHQGIEAMYIGDDQVLAKLELPQEAQAALNDFVWHPGMMDSALQAALGMMDSTEGYPSPRIPFALEEAVIYGPCAPRMWSVIQYSEGNKADDEVLKLDIDLCDDAGRLCAKLKGFSLRAFDRGQGTQKADTLLLAPIWHKQPVDRDKEKEKAPYEQRIVLFCGFEQALGTSMVKHTDYRWLQSEKVGAAERYIDFANQVLNEWQSIIHVGRKQRQCMQLVIPAANDQRSLKGLTAMLKTGQLEHPHVFGQLIEVDELSDIEDILEENIKCQDQHIRYTQGQRWVMKWDDITSQTNMDTVPFKNGCTYLITGGTGGLGLLFAKEIANQVDQATVILVGRSPLDHRQKAALMTIPSNIHAVYECADVSDGNAVKALISDIQQKHGAIHGIIHSAGVVQDSLIRHKTKAELQEVMAAKVEGLILLDQATQNVPLDFFLCFSSGSAVWGSVGQADYAAANAFMDHYMHWRSRLVAVKQRNGRTLSINWPYWKNGGMTIDESTEQMMRGQLGLVPLLNETGIQAFYRAFALDIAQVLVMSGNAERMRQRMIPPKKEPKTVQVQEETSVSQAQASVDLRECMEAALFDVVSQLIHVQMDELDAQTGLDEYGFDSITFSELANELNQRYQLELMPTIFFEHNTLRDLADYLSQTYHAVLKAHFDRVKATMPQTLPAVTEQVADHHHPRSSEKKADERVATKPPARQQQENNNIAIVGMSGLFPGGKDLDDFWENLVAGKDCITEIPNDRWDWREYDGDPLKETNKTNVKWGAFIDGVNQFDPLFFGISPRQAELMDPQQRLLMMYVWKAIEDAGYAPQRLSGSKIGIFAGMGYSGYGSVIKKADSALEGYSATGMAAAMGPNRMSYFLNVHGPSEPIDTACSSSLVAIDRAVNAIQNGYCDSAIAGGVNLILTPELHISFSKANMLSEDGRCKTFSEKANGYVRGEGIGMIFLKKLEDAERAGDHIYGVIKGTSVNHGGRANSLTAPNPKAQSDLLIDAYQKAGIDPRTVTYIEAHGTGTELGDPIEINGLKTAFAHLYAATGEPTVKDAHCGLGSIKSNIGHLELAAGIAGVFKLLLQLKHKKLVKSLHADVINPYIQLEDSPFYIVQSNREWTALKDQEGNDLPRRAGVSSFGFGGVNAHVVIEEYIPSKTASTEGSALSHAPAIILLSAKDDSRLKEQAQNLWLAIRKGDYDDGVLADLAYTLQVGRDAMEERLGLLVTSIQELSEKLKKYLNGKQGISGLYRGQATKQKGPMAALQADDDFHETLSHWLHKGKYHKLISMWVNGIPIDWDELYASKRPKRISLPTYPFARERYWVKETGNVQAVTQPSAIEKKILRKTWRKDTAQGERMPLAGTLIVLATSPTIQMIKPMLADQDVNIIPVVHGDVADQGVATDYYSQEAGETLYQQLKQIIEGPAFQGMIDLTAYDGEYEQDTRIEWGKITFLQHLIAHQGQAGWKVIQVTYSLQSLQIEQPTLQGARLAGLYRMLGAEYKQTRFITMDSDCTAEESQRLWVQVKETFRQQTGITEYCYRQGQRFLPEMMEVSKPEEPAMTAYNEEDVILITGGSRGIGAQIAERVISQGAKHLVIMGREALPDQSMWSEVLAKEENSPLAHKVRHLKSLKDQGIQVLYDHTALTDSEGLKLMVNKIHQQMGPITGVFHCAGIKGENPSFIKKTIQEMQAVCEPKIIGLTHLHKALADEPLAFFLLFSSVASVVPFLAAGQSDYAMANAYMDFYAAYQAGQGKTCFQSIQWPAWKETGMAAGGMETPAYVMSGLQSHNTEDGLHLMEIVRQLHEPVCMPAVIDPVRFASDELLYLKGPVSGHPTAIRKEVAGQRMEKTVMEERAGVMKWLKQLFQKELKLAKTPDEETSFADYGVDSIIIAQIVQIIQEEIGQTLPPSLLLERDTIAALADYLTEHHRAAFQTQSATKADKEVKVSSEPGVSNKLVPQHQEDMAIVGIASRFPDAPNKEAYWELLKQEKRAIRPVPKTRWTAKDGRREDGGWITGIDQFDPDFFNINLADAAIMDPQARLLLEESLKTIYDAGYDHRDLRGKAVGVYIGGRSQPVAPVDQVLQSANPILGMGQNYLAANISKFFDFRGPSMVIDTACSSGMTGLLMAADALRAGRIDMALVGAVSLLLSPMAHDVFAARNILSQNGRFEMFDKQSTGEVLGEGIGIVMVKRLSDAIRDGNHIYGVVKGIAVNNDGRTLGPGSPSLQAQEQVMKEALALSGKKQQDIGYIELNGGGTPIMDTIEIKALSEAYDLTNQELGQVYLGATKPNIGHLLLASGMASFIRCLLSVYHGEIPPFLSAKVPFDHYDFAKSRIQFNRESVAWSTSDNRPRTAALSSFPDGGTNYHVIIESFTPNKVSQLSPKTPPVLQNRQITGIASVEEEVKQEEVQLAGNVWGEIR
>NZ_CP051462.1|WP_084994511.1|1046269_1050376_+|hypothetical-protein
MTKIFRLTLTVDHPIIQHHKVFDQPLLPGLAYIDLLYQLAERLGLEYREYMLKRLSILNPLTVSADRPVPLAITFEETGSHWQIRVESEYKNEQDNIAYITAELHSETVTFNEPIDLGGLQKAATRHFDIDQVYEQAREQGLVHGGAIKAQGDIYQDDNGILIAIEVDEAHQQEANRYLFHPALIDGSAMAAGALWEQPGKGDDLYLPLHYASFYCTAPLQKQGYVRALASSVKKVNDICTLDMFFYNDEGKQIGQLLGITSKKIRTKGQINAALQEQVRPSFAAKEEVAATEQPKQQIKSNGREAAFEHMLREIFARHLNTAPMKVRADQGYFELGLQSSQLLAVMQEVESELGVALSPTLLFEYATIQELSRYLAENVPLPSGWEEAEDEKEVQGEEVNDPAFQAKAAPKISIGEQNEDIAIIGMAGRFPGAATIAEFWGNLVDGKDCITEVPPSRWDWKQFSHLTSPSGKPISRWGGFIDDADCFDPYFFSIAPREAEILDPQERLFLEVCWECIEDAGYVPKTLANESGGNQSRPVGVFVGVMHKDYTLIGAEAAAKGMPIPLSLNYAPIANRVSYFCNFNGPSMAIDTVCSSSLVSVHLAIESIRKGESDVALAGGVNLSLHPNKYLTYGMANMHASDGYCHTFGKGGDGYVSSDGVGVVLLKPLTKAIRDQDHIYAVIKGSAVNHGGRASGITVPNPVAQGDLIASCLAEAKIDPRTISYVEAHGTGTSLGDPIEIQGLIRAYRQYTSEKQYCAIGSVKSNIGHAESAAGIIGLIKNALQLYHKTLVPSLHSEELNPYISFGESPFYVQQQTENWDQPTITKGDETITLPRRAGLSSFGATGTNVHIIMEEGPVPIPQRASHQKVLVPISAKSEERLLAYGEKLLNYLNQLEDDNRLKIADLAYTLQVGRVALEERVAFIVKDHDDFKQKLDSFLAGQDNKQGIYRGHTQQKAELLDLLTEDEDGQDVILKWREKGKLSHIARLWVSGMDVDWQSFYPQDQPHRLSLPTYPFTRERFWIPNVPSATDKPTSLHPLLHHNTSDFSGVRFSSRFTGREPLLSEYMVKGQPALPVPTFIEMVQQAILQAGGEEITDITQVVLNEVSCLEPLLIDTSPFEVHLRLFMENDVINFVMYDNTNIDEPISQGQAFTRIPLEPPVVAIGTLITSSQEINKNLDLPLSSMGMDLGPGYQVIEKVYQGENQLVLKIHLSNTAQQLQEHLMTQPVLLNASLQAARVMLVDTDFHDKPIFWQSETIEYFHANEPEWAVITPNNQQGKWDIQLCTANGRVCVRVTGIHWVNKDGHHVKGADVLSAGEEVMMMSSAYESQMDNLQRLLPNIPSPAIARIDTPNGQRARSKTAFSDR
>NZ_CP051462.1|WP_168767776.1|1050601_1058575_+|SDR-family-NAD(P)-dependent-oxidoreductase
MVELERLFSKLLWRQLQSMGMFTNKHFHIKDVAKQYGLRESYKRWLEASIRFLAEKEYLAWDGQTGVVMDPAPRPMDIVWKEWDEQKQPWLAETNTRAQVVLVEAMMRSLPDILTGKKLATDTMFPQSSFELVEGIYKNNVVVDYFNDVLAAILVNYCNLLRQQHPSAKINILEIGAGTGGTSAGIFEKLAPNSEAIGEYCYTDISKAFLLSAEKAFYTDYPYTTYRTLNIEAPIEQQGFQPGIYDVVVAANVLHATRDIKRTLANTKSLLRKNGLLLINEISQLSLFTHLTFGLTDGWWLYDDAALRIPGCPGLYPETWQKVLEEGGFRSVLFPAEASHNLGQQIIAAESDGVIRLKKSSTEPLQRKEKQGKETVKPSSSPSLSVTGVEEYIADMILEQVADSLKMSQGKVDKNLSFAEYGVDSIIGVRLIQALNDALGIELQTTDLFDYTSVKLLTDYITSNYKEEIASKITVEQLQEEDHEYTQQVVNYPATPKIKTNGYANRSANQTSKSNQSSNGNGPIAIIGMSGRFPQAPTVDALWQQLIKGENLVSKVTRWDLSQYYGEGAAFCDYGAYLEDIDQFDPLFFNISGMEATYMDPQQRLFLLEAWKAMENAGYVGDSVKGRNCGVYVGCGGGDYTSLFVDSPPPQALWGALNSAIPARIAYLLNLKGPAVAVDTACSSSLVALHMSCQSLWSGETEMALAGGVYINNTPQYHLLADKAGMLSQQGRCFTFDDRADGMVPGEAVGAVVLKRLDDAIRDGDHIYGVIQGSGINQDGTTNGITAPSLRSQQHLEESVYETFDINPEEIQMVEAHGTGTKLGDPIEFHALNRSFRSYTDQKGYCALGSIKTNIGHTQLAAGISGLIKILLSLSHKQIPPSLHFEKENANIQLKDSPFFVNTELKEWEVKPGIKRRAALSSFGATGTNAHMVIEEAPELIREHPEKPAYLFVLSARTEERLHKQVEQFITYCEHVGSVDCGNISYTLLFGRQHFKYRLACVAPDLVTARQALLSWAQKGYADSVYVGENQEQREKPTFKQLGNQSIRQCQVSDTEYLDNLSTVADLFVQGYELDYPALFANGQYSRVPLPTYPFAMERYWVPQPDADVAPAREATVKAAPTQPQAAEEVAASTEESQLMTFAESWQRQDLTDERMPLPAVWVCFLSNPTHQQALRTVLQTRYPETEVIFVAQGTAERRESPHHYQLNREDGVAYRQTLQRIAADWGPGFALLYLWPLEDPAVISDYMPLFHLFQAVREAKPARFLWAGEWTTPLERSYLESWIGWERSLGLILPQMGVAGVLQKAAPEMDMAKWLNRLADELASPAIESVFYEGEQRHVCRMEPTDTTEGEGRGLIKEGGTYLITGGGGGLGRRLAANLTRSQSVNLVLTGRSPLSAALAAEIKQWEGTGSHVIYCQADVCDRAAMADVQQKAMTRFGGIDGVIHAAGLASKEPFFAKSAADFACVLAPKVQGAQVLDEVLTPESLDFVCYFSSSSAILGDMGAGDYAMANRFLIAYAHQRQTVYPGKTLVIQWPLWKEGGMGLGDDEQTHMYLASSGQQALETEEGLALFERLLGQASTQHLVLKGQPDRVHRFLGLGQTAAGESSPERLVARNLPAGQGRSEEMKGLSVRQCVEWDLKEIASSLLQIPRNQLHLESNLADFGFDSITLATFAERLTAHYQVEITPALFFGYPTLGKLADYYQTEHAEAMAAFYREGTTTMEKPSSPMLADRQREQKAKPQPAMPEKRTEQPLQPKPQVPEAQQELEPIAVIGMSGRFPGARTIDQMWEHLVKGEEQVQPAARWAEEGEQWRFGAVPGVSEFDPAFFEISPREAQSMDPRQRLLLQEAWRALEDAGYGAKQIKRHRIGMFVGVENGDYQYLSGFQGPITANHDAILAARLSYVLNLNGPNMAINTACSSGLVGLHQACQSLRMGDCDTAIAAGVNLILMPQTLEAIDQAGMLSPDGRCYAFDERANGMVPGEAVAVVVLKRLSQAEADKDPIYAVIRGSGINHDGKTNGITAPNGVVQAQLYRSVYDQYGIHPESLSYVVTHGTGTRLGDPVEINGLRDAFRSYTDKEGFCAITSTKTNFGHTFAASGLVSLISMVQAMRHETIPASLHCEQENRYIQWENSPFYVNKTNQEWKGSAGNPRRGAVSAFGMSGTNVHLVVESYPKEVQATKKSSLPYYLLALSAKTEEALTEKRTDLIAFLESPEGQEADLSQISYTLLQGRQHFRHRWAMVVQGREDALFALKQAINKEDAPNLLQGQVPASFTGQSAIKKYIANLLQESHAVRKEPQQYQENLMALASMYCQGYEMDWAALFAGTDPQCLHMPTYPFARNTYWVVENEQEMPLSIRKKMDFLSEETMHPVRKQTEEIEQEGFRQHVLQHLTTPDPNTWSSEPIAKPEAIQLTGLAKDKTKEEKRNSNKRDVENIEETLVTILKEVLDLDNVDRKMPFIEMGMDSIVGVEWIQAVNERYQTSLTVNSIYEYPNIHKFAKIFAQEDISDAKNDPKIDLAPAVEPTPKQDDPPVTNTIEAIQSFLVASLAESLSMDQKDIELDGELVELGLDSIIGVEWIQTINERYRVELTANTIYEYPYLREFAAFIHGQLAGQMEDKTADSASLQLQKLIHSVQAGEIDIEQADQLLQRGDIRK
>NZ_CP051462.1|WP_084993610.1|1058571_1059789_+|polyketide-beta-ketoacyl:ACP-synthase
MKTELVITGIGVLSAIGQGKADFSSSLLEGKHSFGQMKRPGRQKEIAFIGAEIEELIYQDDSAEKRWRRASLTSQAALLTLMEAWQEAELDHVPAERIGLIVGGSNMQQREMFNIFETYHHKPHFISPTYGMSFMDSDVCGWCTEQFNIKGVACTIGGSSASGQLAVIQACEAVLSGQVDACIALGALMDISYMECHAFRSLGAMGTDLYAHQPEEASRPFDQNRDGFIYGENCGAVVIERKETALKRGIRPYARLLGWGRAMDGNRNPNPSREGEQRVIQQALGQANLSSKSIDYINPHGTGSLIGDETELQALRDCELTHAYINATKSITGHGLSAAGVVELIATLLQMEAGQLHPTRNLQDPMDASFNWVRQEKIAVPIIHSLNLSFGFGGINTAVCLKNER
>NZ_CP051462.1|WP_084993614.1|1061067_1061829_+|enoyl-CoA-hydratase/isomerase
MDYQTVNVRIEQDICYLQLYRPKENNTINDRMIEECHHVLDRYEESITLLVLEGLPDVFCFGADFQEMHDTMTRGQVRERNPERLYDLWLRLATGPFITISHVRGRVNAGGIGFVAASDIVLAERSAQFSLSELLFGVFPAAVLPFLIRRMGVAKANYLTIMTKSITAEQADAWGLVDAYEDNSHSLLRKHLLRLKPLTKRAIVRYKQYIHQLYIPLQEAKSLAVEANKEMFSDTQNLSGIFRYIETGKFPWE
>NZ_CP051462.1|WP_019713718.1|1061854_1062604_+|PRK07110-family-protein
MVTSVVHFQELEPEIVLLRMQDQVHKNTFSKALIDGLLDAFEAIQASETYKVVILTGYDTYFASGGTREGLLAIHEGREKFTDKNVYSLALNCNIPVIAAMQGHGIGGGLIMGLFADFVILSRESVYTTNFMKYGFTPGMGATCILPRKLGISLTEELLINSGTYRGAELEKRGIPFPVLPRVEVLDYAIDLAREIAEKPRYSLVLLKDHLVSPIRKELPAIIEKEVLMHEKTFHQPEVRKRINNLFGK
>NZ_CP051462.1|WP_168767777.1|1062622_1064434_+|hypothetical-protein
MDTKAIFRALQAGDITVQHAYDELASFLNQSEQVEGGDRGNLNDEEKGGPMQDSVVDLQEIEPGIVQVTMQERIHKNTFSTELITGLIQAFESLRANRNCKVVILTGYDTYFACGGTQEGLQALYEGKAKMTDLHLYSMPLECDVPIIAAMQGHGLGGGLCLGLFCDFVIMSRESTYACNHMSYGFTPGDGATLILPRVLGQPLAQELLFTGKNIKGADLADRGAVVPILPRKDVLPYAIKMARELAEKPRESLMLLKQHMVTPLKEALTEVVEKEWAMQEKTLVNRREVLEKMLPAFDSPSNKSSYPELLHLNQHFTGKPVFWLHGEGGGVEGYQWLAEKSRRPFYGIQAPGHMTEHAPIKGVKSMAAYYVTLIQSKQAEGPYDLGGYSLGGVLAYEVTRQLQEAGETVQSLVMLDTPDPFSWEKIRLSSESRALQAMNMALLNRNRKEADGILQKLIHHKEIPEHTDEESLLMQLIRLGRERGLSLTLSETALLKLFQRHLRMQEAFELNQYTLSPLPRASEVTCYYVRNQSGLFYGELMPYLTTDADEITIDHTCYWAEWEKLLPLFHTLDVSSTSHVTILFDRDAQTDIGLLFEKLYDL
>NZ_CP051462.1|WP_168767778.1|1064459_1065302_+|sugar-phosphate-isomerase/epimerase
MMKFSLMTYSMVSLMRSGEMNLEDVIAFAANEGFDAIELLMVNFSRSSDEIRRMLETHQMKISCIDAFVDLAAQQEENFLENISLSQRIIDQAVELSAPMVMLVPGFPDLIASEKDKQQALPRIISALQKITPYAQSKGIVLTIENYSALQMPFCSIAEVLTILEQVPGLRLTLDYGNMLVAGEDPLEAYEKLRKYIVNAHLKDWKVTSGQTGTRCADGRHLEPSLHGQGVINFKSLFAEMVSNNYKGYLSFEYEGDINAKEAVRLGMKHLREQLNEVIG

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Crispr_ID: NZ_CP051462_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP051462_3

3086907-3087014

Orphan

Consensus_repeat	Method
TGATGGGAATCGAACCCACGACAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP051462_3

>merge|NZ_CP051462|3|3086907-3087014|CRISPRCasFinder
TGATGGGAATCGAACCCACGACATCAGCTTGGAAGGCTGAGGTTTTACCACTAAACTACACCCGCAATTTTTATTTGGGGCGATTGATGGGAATCGAACCCACGAATG

>NZ_CP051462|3|3|3086907-3087014|CRISPRCasFinder
TGATGGGAATCGAACCCACGACAT	CAGCTTGGAAGGCTGAGGTTTTACCACTAAACTACACCCGCAATTTTTATTTGGGGCGAT
TGATGGGAATCGAACCCACGAATG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP051462.1\|WP_003242255.1\|3102315_3102861_+\|biofilm-surface-layer-protein-BslA	unknown	unknown	gnl\|CDD\|379999
NZ_CP051462.1\|WP_084995492.1\|3097509_3097998_+\|DinB-family-protein	unknown	unknown	gnl\|CDD\|378981
NZ_CP051462.1\|WP_084995487.1\|3099894_3101367_-\|betaine-aldehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|143437
NZ_CP051462.1\|WP_084992799.1\|3072794_3073619_-\|2-succinyl-6-hydroxy-2,-4-cyclohexadiene-1-carboxylate-synthase	unknown	unknown	gnl\|CDD\|274729
NZ_CP051462.1\|WP_080429054.1\|3082213_3083245_-\|glucose-1-phosphate-adenylyltransferase-subunit-GlgD	unknown	unknown	gnl\|CDD\|273966
NZ_CP051462.1\|WP_084995490.1\|3098003_3098582_-\|MOSC-domain-containing-protein	unknown	unknown	gnl\|CDD\|377051
NZ_CP051462.1\|WP_084992788.1\|3083267_3084410_-\|glucose-1-phosphate-adenylyltransferase	unknown	unknown	gnl\|CDD\|179997
NZ_CP051462.1\|WP_084992798.1\|3073606_3075349_-\|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase	unknown	unknown	gnl\|CDD\|224087
NZ_CP051462.1\|WP_084992790.1\|3080762_3082217_-\|glycogen-synthase-GlgA	unknown	unknown	gnl\|CDD\|234809
NZ_CP051462.1\|WP_084995503.1\|3098669_3099878_-\|choline-dehydrogenase	unknown	unknown	gnl\|CDD\|341481
NZ_CP051462.1\|WP_084992795.1\|3077881_3078349_+\|TspO/MBR-family-protein	unknown	unknown	gnl\|CDD\|226007
NZ_CP051462.1\|WP_084995497.1\|3095270_3096800_-\|flotillin-lipid-rafts-scaffold-protein-FloT	unknown	unknown	gnl\|CDD\|225177
NZ_CP051462.1\|WP_084995501.1\|3094104_3094683_+\|energy-coupled-thiamine-transporter-ThiT	unknown	unknown	gnl\|CDD\|226377
NZ_CP051462.1\|WP_084992796.1\|3075345_3076761_-\|isochorismate-synthase-MenF	unknown	unknown	gnl\|CDD\|224091
NZ_CP051462.1\|WP_003238073.1\|3077052_3077772_+\|yteA-family-sporulation-protein	unknown	unknown	gnl\|CDD\|274340
NZ_CP051462.1\|WP_084992786.1\|3084406_3086290_-\|1,4-alpha-glucan-branching-enzyme	unknown	unknown	gnl\|CDD\|273667
NZ_CP051462.1\|WP_084995499.1\|3094724_3095246_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP051462.1\|WP_084992792.1\|3078379_3080776_-\|glycogen/starch/alpha-glucan-phosphorylase	unknown	unknown	gnl\|CDD\|340853
NZ_CP051462.1\|WP_084995495.1\|3096818_3097343_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376684
NZ_CP051462.1\|WP_084995485.1\|3101565_3102108_+\|transcriptional-regulator-GbsR	unknown	unknown	gnl\|CDD\|224427

Protein	Function_ID	Function_description	E-value
NZ_CP051462.1\|WP_003242255.1\|3102315_3102861_+\|biofilm-surface-layer-protein-BslA	gnl\|CDD\|379999	pfam17735, BslA, Biofilm surface layer A. This family includes members such as BslA (previously called YuaB). Secreted BslA from Bacillus subtillis has been shown to form surface layers around the biofilm self-assembling at interfaces of B. subtilis biofilms, forming an elastic film. structural analysis revealed that BslA consists of an Ig-type fold with the addition of an unusual, extremely hydrophobic cap region. The hydrophobic cap exhibits physiochemical properties similar to the hydrophobic surface found in fungal hydrophobins; thus, BslA is defined as member of a class of bacterially produced hydrophobins.	1.21455e-46
NZ_CP051462.1\|WP_084995492.1\|3097509_3097998_+\|DinB-family-protein	gnl\|CDD\|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	2.63117e-18
NZ_CP051462.1\|WP_084995487.1\|3099894_3101367_-\|betaine-aldehyde-dehydrogenase	gnl\|CDD\|143437	cd07119, ALDH_BADH-GbsA, Bacillus subtilis NAD+-dependent betaine aldehyde dehydrogenase-like. Included in this CD is the NAD+-dependent, betaine aldehyde dehydrogenase (BADH, GbsA, EC=1.2.1.8) of Bacillus subtilis involved in the synthesis of the osmoprotectant glycine betaine from choline or glycine betaine aldehyde.	0
NZ_CP051462.1\|WP_084992799.1\|3072794_3073619_-\|2-succinyl-6-hydroxy-2,-4-cyclohexadiene-1-carboxylate-synthase	gnl\|CDD\|274729	TIGR03695, menH_SHCHC, 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase. This protein catalyzes the formation of SHCHC, or (1 R,6 R)-2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate, by elmination of pyruvate from 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate (SEPHCHC). Note that SHCHC synthase activity previously was attributed to MenD, which in fact is SEPHCHC synthase. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	1.58474e-123
NZ_CP051462.1\|WP_080429054.1\|3082213_3083245_-\|glucose-1-phosphate-adenylyltransferase-subunit-GlgD	gnl\|CDD\|273966	TIGR02092, Glycogen_biosynthesis_protein_GlgD, glucose-1-phosphate adenylyltransferase, GlgD subunit. This family is GlgD, an apparent regulatory protein that appears in an alpha2/beta2 heterotetramer with GlgC (glucose-1-phosphate adenylyltransferase, TIGR02091) in a subset of bacteria that use GlgC for glycogen biosynthesis. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP051462.1\|WP_084995490.1\|3098003_3098582_-\|MOSC-domain-containing-protein	gnl\|CDD\|377051	pfam03473, MOSC, MOSC domain. The MOSC (MOCO sulfurase C-terminal) domain is a superfamily of beta-strand-rich domains identified in the molybdenum cofactor sulfurase and several other proteins from both prokaryotes and eukaryotes. These MOSC domains contain an absolutely conserved cysteine and occur either as stand-alone forms or fused to other domains such as NifS-like catalytic domain in Molybdenum cofactor sulfurase. The MOSC domain is predicted to be a sulfur-carrier domain that receives sulfur abstracted by the pyridoxal phosphate-dependent NifS-like enzymes, on its conserved cysteine, and delivers it for the formation of diverse sulfur-metal clusters.	6.47616e-06
NZ_CP051462.1\|WP_084992788.1\|3083267_3084410_-\|glucose-1-phosphate-adenylyltransferase	gnl\|CDD\|179997	PRK05293, glgC, glucose-1-phosphate adenylyltransferase; Provisional.	0
NZ_CP051462.1\|WP_084992798.1\|3073606_3075349_-\|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase	gnl\|CDD\|224087	COG1165, MenD, 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase [Coenzyme metabolism].	0
NZ_CP051462.1\|WP_084992790.1\|3080762_3082217_-\|glycogen-synthase-GlgA	gnl\|CDD\|234809	PRK00654, glgA, glycogen synthase GlgA.	0
NZ_CP051462.1\|WP_084995503.1\|3098669_3099878_-\|choline-dehydrogenase	gnl\|CDD\|341481	cd08551, Fe-ADH, iron-containing alcohol dehydrogenases (Fe-ADH)-like. This family contains large metal-containing alcohol dehydrogenases (ADH), known as iron-containing alcohol dehydrogenases. They contain a dehydroquinate synthase-like protein structural fold and mostly contain iron. They are distinct from other alcohol dehydrogenases which contains different protein domains. There are several distinct families of alcohol dehydrogenases: Zinc-containing long-chain alcohol dehydrogenases, insect-type, or short-chain alcohol dehydrogenases, iron-containing alcohol dehydrogenases, among others. The iron-containing family has a Rossmann fold-like topology that resembles the fold of the zinc-dependent alcohol dehydrogenases, but lacks sequence homology, and differs in strand arrangement. ADH catalyzes the reversible oxidation of alcohol to acetaldehyde with the simultaneous reduction of NAD(P)+ to NAD(P)H.	4.34726e-175
NZ_CP051462.1\|WP_084992795.1\|3077881_3078349_+\|TspO/MBR-family-protein	gnl\|CDD\|226007	COG3476, COG3476, Tryptophan-rich sensory protein (mitochondrial benzodiazepine receptor homolog) [Signal transduction mechanisms].	1.49995e-40
NZ_CP051462.1\|WP_084995497.1\|3095270_3096800_-\|flotillin-lipid-rafts-scaffold-protein-FloT	gnl\|CDD\|225177	COG2268, COG2268, Uncharacterized protein conserved in bacteria [Function unknown].	1.13413e-120
NZ_CP051462.1\|WP_084995501.1\|3094104_3094683_+\|energy-coupled-thiamine-transporter-ThiT	gnl\|CDD\|226377	COG3859, COG3859, Predicted membrane protein [Function unknown].	3.31732e-70
NZ_CP051462.1\|WP_084992796.1\|3075345_3076761_-\|isochorismate-synthase-MenF	gnl\|CDD\|224091	COG1169, MenF, Isochorismate synthase [Coenzyme metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	7.31596e-164
NZ_CP051462.1\|WP_003238073.1\|3077052_3077772_+\|yteA-family-sporulation-protein	gnl\|CDD\|274340	TIGR02890, conserved_hypothetical_protein, regulatory protein, yteA family. Members of this predicted regulatory protein are found only in endospore-forming members of the Firmicutes group of bacteria, and in nearly every such species; Clostridium perfringens seems to be an exception. The member from Bacillus subtilis, the model system for the study of the sporulation program, has been designated both yteA and yzwB. Some (but not all) members of this family show a strong sequence match to Pfam family pfam01258 the C4-type zinc finger protein, DksA/TraR family, but only one of the four key Cys residues is conserved. All members of this protein family share an additional C-terminal domain. Smaller proteins from the proteobacteria with just the N-terminal domain, including DksA and DksA2 are RNA polymerase-binding regulatory proteins even if the Zn-binding site is not conserved. [Unknown function, General].	2.7197e-68
NZ_CP051462.1\|WP_084992786.1\|3084406_3086290_-\|1,4-alpha-glucan-branching-enzyme	gnl\|CDD\|273667	TIGR01515, branching_enzym, alpha-1,4-glucan:alpha-1,4-glucan 6-glycosyltransferase. This model describes the glycogen branching enzymes which are responsible for the transfer of chains of approx. 7 alpha(1--4)-linked glucosyl residues to other similar chains (in new alpha(1--6) linkages) in the biosynthesis of glycogen. This enzyme is a member of the broader amylase family of starch hydrolases which fold as (beta/alpha)8 barrels, the so-called TIM-barrel structure. All of the sequences comprising the seed of this model have been experimentally characterized. This model encompasses both bacterial and eukaryotic species. No archaea have this enzyme, although Aquifex aolicus does. Two species, Bacillus thuringiensis and Clostridium perfringens have two sequences each which are annotated as amylases. These annotations are aparrently in error. GP\|18143720 from C. perfringens, for instance, contains the note "674 aa, similar to gp:A14658_1 amylase (1,4-alpha-glucan branching enzyme (EC 2.4.1.18) ) from Bacillus thuringiensis (648 aa); 51.1% identity in 632 aa overlap." A branching enzyme from Porphyromonas gingivales, OMNI\|PG1793, appears to be more closely related to the eukaryotic species (across a deep phylogenetic split) and may represent an instance of lateral transfer from this species' host. A sequence from Arabidopsis thaliana, GP\|9294564, scores just above trusted, but appears either to contain corrupt sequence or, more likely, to be a pseudogene as some of the conserved catalytic residues common to the alpha amylase family are not conserved here. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP051462.1\|WP_084995499.1\|3094724_3095246_-\|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.	4.84685e-10
NZ_CP051462.1\|WP_084992792.1\|3078379_3080776_-\|glycogen/starch/alpha-glucan-phosphorylase	gnl\|CDD\|340853	cd04300, GT35_Glycogen_Phosphorylase, glycogen phosphorylase and similar proteins. This is a family of oligosaccharide phosphorylases. It includes yeast and mammalian glycogen phosphorylases, plant starch/glucan phosphorylase, as well as the maltodextrin phosphorylases of bacteria. The members of this family catalyze the breakdown of oligosaccharides into glucose-1-phosphate units. They are important allosteric enzymes in carbohydrate metabolism. The allosteric control mechanisms of yeast and mammalian members of this family are different from that of bacterial members. The members of this family belong to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	0
NZ_CP051462.1\|WP_084995495.1\|3096818_3097343_-\|hypothetical-protein	gnl\|CDD\|376684	pfam01957, NfeD, NfeD-like C-terminal, partner-binding. NfeD-like proteins are widely distributed throughout prokaryotes and are frequently associated with genes encoding stomatin-like proteins (slipins). There appear to be three major groups: an ancestral group with only an N-terminal serine protease domain and this C-terminal beta sheet-rich domain which is structurally very similar to the OB-fold domain, associated with its neighboring slipin cluster; a second major group with an additional middle, membrane-spanning domain, associated in some species with eoslipin and in others with yqfA; a final 'artificial' group which unites truncated forms lacking the protease region and associated with their ancestral gene partner, either yqfA or eoslipin. This NefD, C-terminal, domain appears to be the major one for relating to the associated protein. NfeD homologs are clearly reliant on their conserved gene neighbor which is assumed to be necessary for function, either through direct physical interaction or by functioning in the same pathway, possibly involve with lipid-rafts.	0.000264028
NZ_CP051462.1\|WP_084995485.1\|3101565_3102108_+\|transcriptional-regulator-GbsR	gnl\|CDD\|224427	COG1510, COG1510, Predicted transcriptional regulators [Transcription].	1.29397e-69

>NZ_CP051462.1|WP_084992786.1|3084406_3086290_-|1,4-alpha-glucan-branching-enzyme
MAAASPTAHDVYLFHEGSLFKSYQLFGSHNRELNGQSGYEFCVWAPHASEVRVAGDFNSWSGEQHVMHRVNDNGIWTLFIPGLGEKERYKYEIVTHSGEIRLKADPYAIYSEVRPHTASLTYDLGEYSWKDQLWQKKQKAKTVYEKPVFIYELHLGSWKKHSDGRHYSYKELCQSLIPYIKEHGFTHIELLPVYEHPYDRSWGYQGTGYYSPTSRFGTPHDFMKFVDECHQENIGVILDWVPGHFCKDAHGLYMFDGVPLYEYPEERDRENWLWGTANFDLGKPEVHSFLISNALYWAEFYHIDGFRVDAVANILYWPNQDERHTNPYAVEFLKKLNQTMREAYPHVMMIAEDSTEWPQVTGAVEEGGLGFHFKWNMGWMNDVLTYMETPPEERRNCHQLISFSLLYAFSEHFVLPFSHDEVVYGKKSLLNKMPGDYWQKFAQYRLLLGYMTAHPGKKLIFMGSEFAQFDEWKDTEQLDWFLDSFPMHQKASVFMQDLLRFYQKSKILYENDHRAQSFEWIDVHNNEQSIFSFIRYGKRHGEALVIICNFTPAVYHQYDVGVPFLTQYTEVLNSDSETYGGSGQINKKPLAAKKGALHHKPCYITMTIPPYGISILRAVKKRGEIKR
>NZ_CP051462.1|WP_084992788.1|3083267_3084410_-|glucose-1-phosphate-adenylyltransferase
MKKQCVAMLLAGGKGSRLSGLTKHMAKPAVSFGGKYRIIDFTLSNCSNSGIDTVGILTQYQPLELNSYIGIGSAWDLDRYNGGVTVLPPYAESSEVKWYKGTASAIYENLNYLNQYDPEYVLILSGDHIYKMDYGKMLDFHIEKKADVTISVIEVGWEEASRFGIMKTNADGMITHFDEKPKFPKSNLASMGIYIFNWPLLKQYLEMDDRNPYSSHDFGKDIIPLLLEEKKKLSAYPFKGYWKDVGTVQSLWEANMDLLKEDSELKLFERKWKIYSVNPNQPPQFISSDAQVHDSLVNEGCVVYGNVSHSVLFQGVTVGKHSTVKSSVIMPDVTIGEHVVIENAIVPKGLVLPDGAVIRSEKDIQEVLLVSEEFVEKELI
>NZ_CP051462.1|WP_080429054.1|3082213_3083245_-|glucose-1-phosphate-adenylyltransferase-subunit-GlgD
MFNNQMLGVIDETTYKHSLQDLTAQRSLGAIPFAGRYRLIDFMLSNMVNADIRSVAIFPKYRYRSLMDHLGAGKEWDLHRKKDGLFFFPSPHLHQEYDEFGSFRQFSDHLDYFHRSTQQYAVISNSHTVCNIQFQYVLKRHQEVGCDVTEVFQDGQSLQIYIMSTALLKDLIYGHSEKGYKTIQEAVEKESSSLTICPYEYSGYAAVIDSVEKYYTHSMELIQPRFWQQVFLPQQPIYTKVKDEPPTKYGKHSTVKNSLVANGCVLEGEVENCILFRAVHVGKGTKLKNCIVMQKTQIGEECLLEQVISDKDVKIGNATEAAGTAEQPLVLRKGLVQGELMNS
>NZ_CP051462.1|WP_084992790.1|3080762_3082217_-|glycogen-synthase-GlgA
MKVLFAVSECTPFVKSGGLADVAGALPKALARLGNEVAVMLPKYSQIPERWKKRMRKMAKCTVAVGWRQQYCGIEHMAENDVNYYFIDNEYYFNRDSLYGHYDDGERFAFFSRAVLEAAEAVNVQADIVHTHDWHTAMVNYLLKEEYRKHPFYEQMKSVLTIHNLQFQGTFPPDVTHDLLGLEMDHFHYERLECNGFVNFMKAGIIAADHVTTVSPTYRNEILTPYYGEQLEQVLRYRENNVTGILNGIDDSFYQPKSDPYIEAHYDSEHLANKEENKTKLQRRMGLPERHDIPLISMVTRLTKQKGLDLVRRIMHELLEEQDIQLIVLGTGEREFEDYFRYAEFAFHEKCRAYIGFDEPLAHQIYASSDLFLMPSKFEPCGLGQLIALQYGAIPIVRETGGLYDTVRSYQEEEGTGNGFTFSAFNAHDLKFTIERALSFYRQKDVWKSIMKTAMNADYSWEQSAKEYQRIFEHVTRSGRDVLE
>NZ_CP051462.1|WP_084992792.1|3078379_3080776_-|glycogen/starch/alpha-glucan-phosphorylase
MFSSKERFAALFLKRLEMTCGKSFKDSAKLDQYKTLGNMVREYISADWIQTNEKSRSNSGKQTYYLSIEFLLGQLLEQNLMNLGVRDVVEAGLKDIGINLEEIVQMESDAGLGNGGLGRLAACFLDSLASLNLPGHGMGIRYKHGLFEQKIVDGHQVELPEQWLKNGNVWEVRNADQAVDVPFWGEVHMTEKNGRLHFRHEQATIVSAVPYDIPIIGYETGTVNTLRLWNAEPSAHYHGGNILSYKRETEAVSEFLYPDDTHDEGKILRLKQQYFLVCASLKSIVNNYRKTNKSLSGLHKKVSIHINDTHPALAVPELMRILLDEENMSWEEAWHITVHTISYTNHTTLSEALEKWPIHLFKPLLPRMYMIIEEINERFCRAVWEKYPGDWKRIEAMAITAHGVVKMAHLAIVGSYSVNGVAKIHSDILKEREMRDFHLLFPSRFNNKTNGIAHRRWLLKANPGLSAIITEAIGNEWVKQPESLIELESYASDPAFIEQFQNNKSRKKQELADLIFCTAGVVVNPDSIFDVQVKRLHAYKRQLLNVLHIMYLYNRLKEDSGFSIYPQTFIFGAKASPSYHYAKKIIKLIHSVSEKVNYDPAVKQLIKIVFLENYRVSMAERIFPASDVSEQISTASKEASGTGNMKFMMNGALTIGTHDGANIEILERVGPDCIYTFGLKADDVLSYQENGGYRSREYYQHDRRIRQVVDQLINGFFEGEADEFESIYDSLLPHNDEYFVLKDFSSYADAQERIQADYRDRRKWSERSVLNIAHSGYFSSDRTIREYAKDIWGIRPMM
>NZ_CP051462.1|WP_084992795.1|3077881_3078349_+|TspO/MBR-family-protein
MKKIVGAIAVFVITYALFSAADYLFPIDQEWYNSLKKPDWTPPGSAIGIIWAILFALISLSAAIVYAAFSFKDAKSFWIMLLLNYVLNQAFSYFQFTQKNLLAASIDCLLVAITALILMIAAKKYSRAASYLLLPYFLWSAFATFLSFTIYSMNL
>NZ_CP051462.1|WP_003238073.1|3077052_3077772_+|yteA-family-sporulation-protein
MLTKDQLQHLKNELEQTKKDILNRFKDNDHFQLNSAFPYDSWGELSAYDNHPGDQATELYEREKDIALDLHEREHLRDIEHSLKAIENGTYGICEVSGKEIPYERLEALPTATTLAEYSSQDVVSKDRPIEEETPFGQFEFDDDEEIRAPYDSEDSYQDVEKYGNSSTPQDMENPPLSYDDMTMNAEENIGNTESYENFIATDITGKEITVYQSRAHERYEEELDEEGIMTTFGDLHAD
>NZ_CP051462.1|WP_084992796.1|3075345_3076761_-|isochorismate-synthase-MenF
MVTTVQRTFRKEVLHALHKAKEVNHAVLISYSRQIESLDPLSFFNYGAKKYTGNRFFWSDPESELTIVGLGKEAVFQTNQKNSERYREVFEQWERFKKTAFHIYEEEKLQHSAVGPVLFGGFSFDPLEERGTQWDHFSEGDFFVPALMLTMTAEGPFLTVNRWVSEKEDAEAVLEGLKAFAAEFMVPVLEQGDQAAIAASQELDKDDWLKAIETATSQIKEKQYDKVVLARELLLTFDGPVQIEPVLKTLLNDQQTSYVFAIEQEGKTFVGASPERLIKRDGSTVMSTCLAGSIKRGADEEEDRRIGLELLNDEKNLLEHDIVVGMIHNAFISSCSEVEKPDGPALYKTKSVQHLFTPIVGQLRESASLFDLIEKLHPTPALGGAPQKKAVEVIREIEPMSRGWYAAPIGWIDSQDNGEFAVAIRSGLIEGSTARLFAGCGIVEDSDPQSEYEETQIKLKPMISALGGERR
>NZ_CP051462.1|WP_084992798.1|3073606_3075349_-|2-succinyl-5-enolpyruvyl-6-hydroxy-3--cyclohexene-1-carboxylic-acid-synthase
MTANPITHYIGSFMDEFALSGITDAVVCPGSRSTPLAILAAAHPDISVHVQIDERSAGFFALGLAKAKQSPVLLICTSGTAAANFYPAVIEAHYSRVPIIVLTADRPHELREVGAPQAINQHFLFGNFVKFFTDSALPEESPHMLRYIRTLASRAAGEAQKRPMGPVHVNVPLREPLMPDLSAEPFGRMRTGRHVSVKTGTQSVDRESLADVAVMLTEAEKGMIVCGELHSDTDKENIIALSKALQYPILADPLSNLRNGVHDKSTVIDAYDSFLKDDELKAKLRPDVVIRFGPMPVSKPVFLWLKDDPAIQQIVIDEDGGWRDPTQASAHMIHCNASAFAEAIMAELADITRSSEWLEKWQFVNGRFREHLQTISSEEVSFEGNLYRILQHLVPENSSLFVGNSMPIRDVDTFFEKQERDFRIYSNRGANGIDGVVSSAMGVCEGTKAPVTLVIGDLSFYHDLNGLLAAKKLGIPLTVILVNNDGGGIFSFLPQASEKAHFEDLFGTPTGLDFKHAAALYGGTYSCPASWDEFKAAYAPQADKPGLHLIEIKTDRQSRVQLHRDMLNEAVREVKKQWEL
>NZ_CP051462.1|WP_084992799.1|3072794_3073619_-|2-succinyl-6-hydroxy-2,-4-cyclohexadiene-1-carboxylate-synthase
MGTVNLTVSDGVRYAVTDERPNASEAIVCLHGFTGSKQSWNFLDRMLPDSRLIKIDCLGHGETDAPLNGKRYSTSRQVSDLAEIFDQLKLHKVKLIGYSMGGRLVYSFAMTYPERVSALVLESTTPGLKTLEERRERIMRDRKLADFILRNGIKAFVQYWEGIPLFSSQQRLAEDIRHRIRSGRLRNNKIGLANSLTGIGTGSQPSWWSRVDEIAVPVLLICGEWDEKFCAINQEVHKKLPSSRIEIVPNAGHTVHVEQPRFFGKIVSEFLTSI
>NZ_CP051462.1|WP_084995501.1|3094104_3094683_+|energy-coupled-thiamine-transporter-ThiT
MNQSKQLVRLIEIAIMTAAAVILDIVSGMFLRMPQGGSVSIMMIPIFLISFRWSVKAGLTTGLLTGLVQIAIGNLFAQHPVQLLLDYLIAFAAIGLSGFFASSVRKAAVSKTKGKLIVSVVSAVFIGSFLRYAAHVISGAVFFGSFAPKGTPVWIYSLTYNATYMVPSFIICAIVLCLLFMTAPRLLKTDRA
>NZ_CP051462.1|WP_084995499.1|3094724_3095246_-|GNAT-family-N-acetyltransferase
MVILREAKVEDIKDIAKVHVDSWRTTYRGIVPADYLNSLNYKEFEDKWKSRSLKGVFVAQDEKGSIFGFASFGPIRSEQKGYDGELYAIYLLEEHQRQGAGRALLAKGAEFLLHHGFSSMFVWVMEKNPSITFYQSYSPEREAEDSFEIAGERLKEVGFGWPDLSALKTVLNR
>NZ_CP051462.1|WP_084995497.1|3095270_3096800_-|flotillin-lipid-rafts-scaffold-protein-FloT
MTMPIIIVIGVVFFLLIALIAVFITKYRTAGPDEALIVTGSYLGNKNVHVDEGGNRIKIVRGGGTFVLPVFQQAEPLSLLSSKLDVSTPEVYTEQGVPVMADGTAIIKIGGSIGEIATAAEQFLGKSKEDREQEAREVLEGHLRSILGSMTVEEIYKNREKFSQEVQRVASQDLAKMGLVIVSFTIKDVRDKNGYLESLGKPRIAQVKRDADIATAEADKETRIKRAEADKDAKKSELERATEIAEAEKINQLKMAEYRREQDTAKANADQAYDLETARARQQVTEQEMQVKIIERQKQIELEEKEILRRERQYDSEVKKKADADRYSVEQSAAAEKAKQLAEADAKKYSIEAMAKAEAEKVRIDGLAKAEAEKAKGETEAEVIRLKGLAEAEAKEKIAAAFEQYGQAAIFDMIVKMLPEYAKQAAAPLSNIDKITVVDTGGSGELSGANKVTSYATNLMSSLQESLKASSGIDVKEMIENFSGKGNVKQSINELTNEIKEAKTVQKPE
>NZ_CP051462.1|WP_084995495.1|3096818_3097343_-|hypothetical-protein
MELLGVPIQTIYLYTLIIAGSLTLLFLFFGDVFAGLSEGIPLLNPTLVLAFFTCFSAGGYIGELTLPLSSLLLAFLSCILSIILVTLLHIFVLVPLSSAEESLAYKEADLKGRVGKVITAVPVDGFGEVVIEGIGGTISKSAVSFENQQISYGTTVLVVNVNNGVLSVTPHEPI
>NZ_CP051462.1|WP_084995492.1|3097509_3097998_+|DinB-family-protein
MSIFNEARLETWNEVKGLSDEKLNQKPSAEEWSIREVLDHLKKIDMTAQKMLKERIKEAPVKEVEEKPLETAQDRNNKRKAPSHLEPEHDFISGSQMKRELDVVREQLTAAIASLKEEDLKRVLPHPVFQELTVGQWIDFIGHHEKRHLSQIKEIKEKVERV
>NZ_CP051462.1|WP_084995490.1|3098003_3098582_-|MOSC-domain-containing-protein
MWKRMTAKTEGLYIADTESFVTKQMDKLDFDYGGIPGDLHFGLTKKAGAREPMFSKGTEIFNRRQISIVSLEECDQIALKMGVPSILPEWLGANVAVSGIHNFTSLKEGSRLIFPSGAALLCEGENDTCIQPGEVIQSYYPDKPKLAPAFVRHALGIRGIVCIVERPGAVYAGDEIEVHSYQRKVKRKAERV
>NZ_CP051462.1|WP_084995503.1|3098669_3099878_-|choline-dehydrogenase
MTLNMKVESMQKFHTFEIPTVIKHGIGAVKHTGEEVAALGVSKALLVTDPGIYKAGVADPVIESLKEAGIEVVLFNKVEPNPPVRLVNEGSELYKKENCNGLVAVGGGSSMDTAKAIGVEATHEGSVLDYEAADGKKPLENRIPPLTTIPTTAGTGSEVTQWAVITDEEREFKFNTGGPLIAAHLTIIDPELHISMPPHVTAMTGIDALAHAIECYTMKFAQPITDAVALMAIEYAAHYIRRAFADGEDLEARYGMAQAAMLAGLSYGSESAGAAHAMSQTLGGIIPVAHGQCVAAMMGPVMEYNWKGYPEKFARIAKAFGIDTSNMTTEEAAKASVNWMYDLVEDLEVPTLEEQGVSTDMIERLSKEAMKDPQTFGNPRDLNEKAYNWIYKRCFNLTPKTV
>NZ_CP051462.1|WP_084995487.1|3099894_3101367_-|betaine-aldehyde-dehydrogenase
MSQTLYIDGEWISAEKEQIRSIINPFNQEEIATVSEGGREDAIKAIAAARRAFDKGEWASLSGLERGNIVLKIAELIRRDLDELAELESLDTGKTFEESKADMDDIANVFQYYAGLADKDGGEIISSPIPDSESKIIREPIGVCGQITPWNYPLLQASWKIAPALAAGNTIVMKPSEITPLTTIKVFKLMEEAGVPKGVANLVLGPGATVGDELAANKDVDLISFTGGIETGKKIMQAASGNVKKIALELGGKNPNIVFKDADLEVAVDQALNAVFFHAGQVCSAGSRLLVEDAIHDQFLAELVKRAKRIKLGNGFHAETESGPLISAEHRAKVEKYVEIGIQEGAKLETGGKRPEDPALQNGFFYEPTIFSNCKSGMRIVQEEVFGPVLTVETFSSEEEVIALANDTIYGLAGAVWSKDIEKCERVAARLRMGTVWINDFHPYFAQAPWGGYKQSGFGRELGKMGLEEYTEVKHVYRNTKPAAVNWFNS
>NZ_CP051462.1|WP_084995485.1|3101565_3102108_+|transcriptional-regulator-GbsR
MDENPEFATIEQARDLVIDSIAETMDLYGITRSVGILYGTMYMRDEMTLDEMREELQMSKPSMSTGVKKLQDLNVVKKTFHRGIRKHTFVAEKDFFKFFTNFFPPKWEREVQVNVAAIEESQADLQEVLSKEGLSEDIKNEALQLYEQLESSKAYYDWLKRLAESVQSGEIFKFIPIETK
>NZ_CP051462.1|WP_003242255.1|3102315_3102861_+|biofilm-surface-layer-protein-BslA
MKRKLLSSLAISALSLGLLVSAPTASFAAESKSTSAHTESTMRTQSSASLFATITGASKTEWSFSDIELTYRPNTLLSLGVMEFTLPSGFTANTKDTMNGNALRTTQILNNGKTVRIPLALDLLGAGEFKLKLNNKTLPAAGTYTFRAENKSLSIGNKFYAEASIDVAKRSTPPTQPCGCN

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NZ_CP024037	Bacillus aryabhattai strain K13 plasmid unnamed2	10417-10476	7	0.883
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NZ_CP026740	Bacillus megaterium strain YC4-R4 plasmid unnamed4	70764-70823	7	0.883
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NC_017139	Bacillus megaterium WSH-002 plasmid WSH-002_p1, complete sequence	1318-1377	7	0.883
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NZ_CP010587	Bacillus megaterium Q3 plasmid p1, complete sequence	838-897	7	0.883
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NZ_CP023319	Bacillus megaterium strain A plasmid p2, complete sequence	75825-75884	7	0.883
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NC_020451	Vibrio coralliilyticus strain ATCC BAA-450 plasmid, complete sequence	1960-2019	9	0.85
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NZ_CP015440	Anoxybacillus amylolyticus strain DSM 15939 plasmid pDSM15939_2, complete sequence	64773-64832	12	0.8
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NZ_CP033045	Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence	483791-483850	13	0.783
NZ_CP051462_3	3.1\|3086931\|60\|NZ_CP051462\|CRISPRCasFinder	3086931-3086990	60	NZ_LR134399	Listeria monocytogenes strain NCTC7974 plasmid 2, complete sequence	57361-57420	14	0.767

1. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NZ_CP024037 (Bacillus aryabhattai strain K13 plasmid unnamed2) position: , mismatch: 7, identity: 0.883

cagcttggaaggctgaggttttaccactaaactacacccgcaatttttatttggggcgat	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcatatttta-aagtggcggt	Protospacer
******************************************  *****   * ****.*

2. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NZ_CP026740 (Bacillus megaterium strain YC4-R4 plasmid unnamed4) position: , mismatch: 7, identity: 0.883

cagcttggaaggctgaggttttaccactaaactacacccgcaatttttatttggggcgat	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcatatttta-aagtggcggt	Protospacer
******************************************  *****   * ****.*

3. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NC_017139 (Bacillus megaterium WSH-002 plasmid WSH-002_p1, complete sequence) position: , mismatch: 7, identity: 0.883

cagcttggaaggctgaggttttaccactaaactacacccgcaatttttatttggggcgat	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcatatttta-aagtggcggt	Protospacer
******************************************  *****   * ****.*

4. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NZ_CP010587 (Bacillus megaterium Q3 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.883

cagcttggaaggctgaggttttaccactaaactacacccgcaatttttatttggggcgat	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcatatttta-aagtggcggt	Protospacer
******************************************  *****   * ****.*

5. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NZ_CP023319 (Bacillus megaterium strain A plasmid p2, complete sequence) position: , mismatch: 7, identity: 0.883

cagcttggaaggctgaggttttaccactaaactacacccgcaatttttatttggggcgat	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcatatttta-aagtggcggt	Protospacer
******************************************  *****   * ****.*

6. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NC_020451 (Vibrio coralliilyticus strain ATCC BAA-450 plasmid, complete sequence) position: , mismatch: 9, identity: 0.85

cagcttggaaggctgaggttttaccactaaactacacccgcaatttttatttggggcgat	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcattttagttatggcccggg	Protospacer
****************************************** ***   * ***  **.

7. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NZ_CP015440 (Anoxybacillus amylolyticus strain DSM 15939 plasmid pDSM15939_2, complete sequence) position: , mismatch: 12, identity: 0.8

cagcttggaaggctgaggttttaccactaaactacacccgca-------atttttatttg	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcataataatatataccattg	Protospacer
******************************************       ** * .  ***

8. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NZ_CP033045 (Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence) position: , mismatch: 13, identity: 0.783

cagcttggaaggctgaggttttaccactaaactacacccgc--------aatttttattt	CRISPR spacer
cagcttggaaggctgaggttttaccactaaactacacccgcatggttaaaagttttgcca	Protospacer
*****************************************        ** ****...

9. spacer 3.1|3086931|60|NZ_CP051462|CRISPRCasFinder matches to NZ_LR134399 (Listeria monocytogenes strain NCTC7974 plasmid 2, complete sequence) position: , mismatch: 14, identity: 0.767

cagcttggaaggctgaggttttaccactaaactacacccgc---------aatttttatt	CRISPR spacer
cagcttggaaggctgtagttttaccactaaactacacccgcatagtaagtagttcttagt	Protospacer
*************** .************************         *.**.*** *

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

704906 : 714807

Synechococcus_phage(50.0%)

The bacterium proteins that are colored denote the protein is present at specific phage-related keywords (such as 'capsid', 'head', 'integrase', 'plate', 'tail', 'fiber', 'coat', 'transposase', 'portal', 'terminase', 'protease' or 'lysin' and 'tRNA')

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_084990885.1\|704906_706202_+	adenylosuccinate lyase	A0A2H4UUU6	Bodo_saltans_virus	2.0e-19	25.7
WP_084990883.1\|706276_707002_+	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0E3G7P8	Synechococcus_phage	1.6e-45	44.1
WP_003155758.1\|706994_707249_+	phosphoribosylformylglycinamidine synthase subunit PurS	M4QPE7	Synechococcus_phage	4.7e-05	33.3
WP_004397716.1\|707245_707929_+	phosphoribosylformylglycinamidine synthase subunit PurQ	NA	NA	NA	NA
WP_084990881.1\|707912_710141_+	phosphoribosylformylglycinamidine synthase subunit PurL	A6N228	Microbacterium_phage	8.5e-159	40.1
WP_060398068.1\|710116_711547_+	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	1.2e-52	32.5
WP_060398069.1\|711647_712688_+	phosphoribosylformylglycinamidine cyclo-ligase	A0A0E3F760	Synechococcus_phage	6.3e-64	41.1
WP_084990879.1\|712684_713272_+	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	1.6e-27	41.0
WP_084990877.1\|713268_714807_+	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	6.7e-78	53.0

DBSCAN-SWA_2

1365177 : 1409875

Bacillus_phage(33.33%)

tRNA,coat

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_084991358.1\|1365177_1365861_+\|coat	spore coat protein	NA	NA	NA	NA
WP_003239244.1\|1365952_1366402_-\|coat	spore coat protein CotZ	NA	NA	NA	NA
WP_003239243.1\|1366529_1367018_-\|coat	spore coat protein CotY	NA	NA	NA	NA
WP_019258074.1\|1367168_1367684_-\|coat	spore coat protein	NA	NA	NA	NA
WP_019258075.1\|1367772_1368102_-	hypothetical protein	NA	NA	NA	NA
WP_003239240.1\|1368142_1368529_-\|coat	spore coat protein CotV	NA	NA	NA	NA
WP_003239239.1\|1368688_1369045_+	sporulation protein YjcA	NA	NA	NA	NA
WP_084991361.1\|1369328_1369535_+	hypothetical protein	NA	NA	NA	NA
WP_003239234.1\|1369616_1369772_+	sporulation protein YjcZ	NA	NA	NA	NA
WP_003239233.1\|1369904_1370159_+	sporulation-specific transcription regulator SopVIF	NA	NA	NA	NA
WP_142271081.1\|1370237_1372514_-	UvrD-helicase domain-containing protein	A0A068EQC7	Bacillus_phage	4.6e-91	34.8
WP_084991521.1\|1372632_1372887_+	hypothetical protein	NA	NA	NA	NA
WP_084991363.1\|1372960_1373383_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_084991364.1\|1373388_1373904_-	hypothetical protein	NA	NA	NA	NA
WP_084991366.1\|1373940_1374663_-	esterase family protein	NA	NA	NA	NA
WP_029316812.1\|1375019_1376141_+	cystathionine gamma-synthase/O-acetylhomoserine thiolyase	A0A0B5JD48	Pandoravirus	5.6e-18	26.7
WP_084991369.1\|1376133_1377306_+	cystathionine beta-lyase	NA	NA	NA	NA
WP_084991370.1\|1377338_1377881_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_084991371.1\|1377950_1379141_-	DUF819 domain-containing protein	NA	NA	NA	NA
WP_084995748.1\|1380856_1381108_+	hypothetical protein	A0A2H4JA61	uncultured_Caudovirales_phage	9.3e-06	42.9
WP_084995749.1\|1381154_1381430_-	hypothetical protein	O64122	Bacillus_phage	3.9e-05	41.1
WP_084995751.1\|1381700_1382051_-	hypothetical protein	NA	NA	NA	NA
WP_084995765.1\|1384406_1384922_+	sigma-70 family RNA polymerase sigma factor	A0A1L2JY33	Aeribacillus_phage	3.4e-26	41.5
WP_084995755.1\|1385135_1385450_-	hypothetical protein	NA	NA	NA	NA
WP_084995757.1\|1385633_1386320_+	hypothetical protein	NA	NA	NA	NA
WP_168767791.1\|1386404_1386653_+	hypothetical protein	NA	NA	NA	NA
WP_061046862.1\|1388577_1388766_-	hypothetical protein	NA	NA	NA	NA
WP_084995763.1\|1388784_1389636_-	hypothetical protein	NA	NA	NA	NA
WP_168767792.1\|1389900_1390341_-	SMI1/KNR4 family protein	NA	NA	NA	NA
WP_084995593.1\|1391509_1392010_+	hypothetical protein	NA	NA	NA	NA
WP_084995590.1\|1392081_1392816_+	hypothetical protein	NA	NA	NA	NA
WP_084995588.1\|1393868_1394762_-	AraC family transcriptional regulator	NA	NA	NA	NA
WP_084995586.1\|1394965_1395418_+	SnoaL-like domain-containing protein	NA	NA	NA	NA
WP_084995584.1\|1395697_1395823_+	hypothetical protein	NA	NA	NA	NA
WP_084995582.1\|1395986_1397306_+	replication-associated recombination protein A	G3MBE0	Bacillus_virus	5.3e-92	42.5
WP_084995580.1\|1397957_1398278_+	antibiotic biosynthesis monooxygenase	NA	NA	NA	NA
WP_084995258.1\|1398817_1400770_+	BglG family transcription antiterminator	NA	NA	NA	NA
WP_084995255.1\|1400919_1402872_+	PTS mannose transporter subunit IIABC	NA	NA	NA	NA
WP_084995253.1\|1402887_1403835_+	mannose-6-phosphate isomerase, class I	NA	NA	NA	NA
WP_032732176.1\|1404462_1404747_+	hypothetical protein	NA	NA	NA	NA
WP_084995250.1\|1405227_1405641_+	YjdF family protein	NA	NA	NA	NA
WP_084995248.1\|1405669_1406176_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_084995246.1\|1406465_1406861_-	hypothetical protein	NA	NA	NA	NA
WP_084995241.1\|1407127_1407610_+\|tRNA	Cys-tRNA(Pro) deacylase	NA	NA	NA	NA
WP_003239199.1\|1407640_1407835_-	DUF4177 domain-containing protein	NA	NA	NA	NA
WP_084995238.1\|1408526_1409489_-	protoheme IX farnesyltransferase	NA	NA	NA	NA
WP_019258099.1\|1409638_1409875_-\|coat	spore coat protein CotT	NA	NA	NA	NA

DBSCAN-SWA_3

1450405 : 1493782

Bacillus_phage(29.41%)

holin,plate,protease,terminase,portal,tail,capsid

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_080010777.1\|1450405_1451542_+	response regulator aspartate phosphatase RapA	A0A1P8CWN8	Bacillus_phage	8.3e-94	47.1
WP_019258130.1\|1451531_1451666_+	phosphatase RapA inhibitor PhrA	NA	NA	NA	NA
WP_084995158.1\|1451695_1451950_-	hypothetical protein	NA	NA	NA	NA
WP_084995155.1\|1452072_1453026_+	LysM peptidoglycan-binding domain-containing protein	A0A218KC88	Bacillus_phage	5.6e-67	74.1
WP_003239140.1\|1453062_1453440_-	PH domain-containing protein	A5GYQ0	Lactococcus_phage	6.1e-17	43.4
WP_003239139.1\|1453545_1454148_+	poly-gamma-glutamate hydrolase family protein	A0A0Y0AJU6	Bacillus_phage	2.7e-43	48.3
WP_019258134.1\|1454221_1455058_+	manganese catalase	NA	NA	NA	NA
WP_084995154.1\|1455101_1455698_-	ImmA/IrrE family metallo-endopeptidase	A0A2H4JA43	uncultured_Caudovirales_phage	1.6e-40	53.0
WP_084995151.1\|1455859_1456201_-	helix-turn-helix transcriptional regulator	A0A2H4J6F9	uncultured_Caudovirales_phage	1.7e-18	44.9
WP_084995148.1\|1456378_1456558_+	hypothetical protein	NA	NA	NA	NA
WP_084995145.1\|1456544_1457381_+\|portal	phage portal protein	S6BFM4	Thermus_phage	4.3e-23	28.5
WP_084995142.1\|1457280_1458081_+	ATP-binding protein	A6XMI1	Bacillus_virus	9.1e-63	53.0
WP_019258140.1\|1458080_1458248_+	hypothetical protein	NA	NA	NA	NA
WP_084995140.1\|1458332_1458689_+\|portal	phage portal protein	NA	NA	NA	NA
WP_084995137.1\|1458675_1458882_+	phage-like element PBSX protein XtrA	A0A2H4J4M6	uncultured_Caudovirales_phage	9.3e-12	48.5
WP_084995134.1\|1458996_1459506_+	sigma-70 family RNA polymerase sigma factor	A0A1L2JY33	Aeribacillus_phage	1.2e-20	37.4
WP_084995132.1\|1459623_1460421_+\|terminase	terminase	A0A0S2MVB6	Bacillus_phage	4.0e-58	49.4
WP_084995128.1\|1460417_1461719_+\|terminase	PBSX family phage terminase large subunit	A0A2P1JTW5	Anoxybacillus_phage	6.3e-154	60.2
WP_029316818.1\|1461722_1463210_+\|portal	phage portal protein	A0A1B1P7C8	Bacillus_phage	3.8e-139	55.3
WP_084995125.1\|1463229_1464057_+\|portal	phage portal protein	A0A1B1P7E4	Bacillus_phage	3.0e-53	57.7
WP_084995123.1\|1464082_1465018_+\|capsid	major capsid protein	A0A1B1P7E3	Bacillus_phage	3.9e-105	64.1
WP_084995120.1\|1465039_1465423_+	DUF3199 family protein	A0A1B1P7D6	Bacillus_phage	7.1e-13	41.5
WP_084995118.1\|1465419_1465776_+	YqbH/XkdH family protein	A0A249XXE9	Clostridium_phage	7.5e-09	37.7
WP_084995115.1\|1465772_1466258_+	HK97 gp10 family phage protein	NA	NA	NA	NA
WP_084995113.1\|1466271_1466712_+\|portal	phage portal protein	NA	NA	NA	NA
WP_084995110.1\|1466715_1466934_+	hypothetical protein	NA	NA	NA	NA
WP_003239116.1\|1466930_1468331_+	hypothetical protein	A0A0A7RTT5	Clostridium_phage	8.5e-80	39.7
WP_003239114.1\|1468332_1468776_+\|tail	phage tail tube protein	A0A0K2CNG3	Brevibacillus_phage	1.1e-25	45.2
WP_003232676.1\|1468866_1469313_+	phage-like element PBSX protein XkdN	A0A249XXA9	Clostridium_phage	7.5e-14	33.6
WP_003239113.1\|1469342_1469492_+	hypothetical protein	NA	NA	NA	NA
WP_084995107.1\|1469493_1473375_+	transglycosylase SLT domain-containing protein	A0A1L2JY60	Aeribacillus_phage	1.3e-42	44.9
WP_024121074.1\|1473367_1474027_+	LysM peptidoglycan-binding domain-containing protein	A0A090DBR9	Clostridium_phage	2.8e-25	34.0
WP_084995104.1\|1474042_1475020_+\|portal	phage portal protein	H7BV96	unidentified_phage	1.0e-39	32.6
WP_084995102.1\|1475019_1475286_+	DUF2577 family protein	NA	NA	NA	NA
WP_084995099.1\|1475345_1475771_+	DUF2634 domain-containing protein	A0A2H4J6K5	uncultured_Caudovirales_phage	2.3e-12	37.3
WP_084995097.1\|1475763_1476810_+\|plate	baseplate J/gp47 family protein	S6AVU3	Thermus_phage	4.1e-71	43.5
WP_003239106.1\|1476793_1477372_+	YmfQ family protein	A0A2H4J717	uncultured_Caudovirales_phage	1.1e-14	33.8
WP_084995094.1\|1477368_1477641_+	hypothetical protein	NA	NA	NA	NA
WP_084995091.1\|1477643_1479755_+\|terminase	terminase	A0A1P8CWR7	Bacillus_phage	3.0e-44	56.8
WP_084995088.1\|1479765_1480095_+\|portal	phage portal protein	A0A2H4JCI0	uncultured_Caudovirales_phage	1.4e-14	42.3
WP_019258164.1\|1480091_1480256_+	XkdX family protein	A0A2H4JAA1	uncultured_Caudovirales_phage	5.0e-16	69.8
WP_084995084.1\|1480302_1481142_+\|portal	phage portal protein	NA	NA	NA	NA
WP_060398448.1\|1481194_1481464_+	hemolysin XhlA family protein	A0A2H4JD40	uncultured_Caudovirales_phage	3.3e-25	65.9
WP_003239099.1\|1481476_1481740_+\|holin	phage holin	A0A2H4J6M0	uncultured_Caudovirales_phage	3.6e-24	64.4
WP_084995081.1\|1481752_1482646_+	LysM peptidoglycan-binding domain-containing protein	Q9ZXD7	Bacillus_phage	1.2e-82	68.8
WP_119913750.1\|1482682_1482820_-	hypothetical protein	NA	NA	NA	NA
WP_003239095.1\|1482904_1483075_-	type II toxin-antitoxin system SpoIISB family antitoxin	NA	NA	NA	NA
WP_084995078.1\|1483074_1483821_-	toxin-antitoxin-antitoxin system toxin SpoIISA	NA	NA	NA	NA
WP_019258170.1\|1483931_1484933_-	inorganic phosphate transporter	NA	NA	NA	NA
WP_003218470.1\|1484945_1485563_-	DUF47 domain-containing protein	NA	NA	NA	NA
WP_084995075.1\|1485838_1487155_-	serine/threonine exchanger	NA	NA	NA	NA
WP_084995072.1\|1487540_1488491_+	ring-cleaving dioxygenase	NA	NA	NA	NA
WP_142271186.1\|1488591_1488738_+	hypothetical protein	NA	NA	NA	NA
WP_084995069.1\|1488745_1490932_+	glycosyltransferase family 39 protein	NA	NA	NA	NA
WP_084995066.1\|1490943_1491915_+	glycosyltransferase family 2 protein	A0A2H5BFL1	Salmonella_phage	1.1e-62	41.0
WP_084995062.1\|1492411_1493782_-\|protease	serine protease HtrA	A0A1B1IT49	uncultured_Mediterranean_phage	1.2e-22	32.6

DBSCAN-SWA_4

1928119 : 1934906

Bacillus_phage(50.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_084992372.1\|1928119_1928512_+	class Ib ribonucleoside-diphosphate reductase assembly flavoprotein NrdI	G3MBF1	Bacillus_virus	1.1e-29	58.3
WP_003238357.1\|1928471_1930574_+	class 1b ribonucleoside-diphosphate reductase subunit alpha	U5PY35	Bacillus_phage	0.0e+00	87.0
WP_014113879.1\|1930591_1931581_+	class 1b ribonucleoside-diphosphate reductase subunit beta	F8WQ21	Bacillus_phage	1.1e-155	84.1
WP_084992370.1\|1931628_1932249_+	hypothetical protein	A0A127AYS1	Bacillus_phage	1.2e-46	48.4
WP_019258473.1\|1932310_1933078_-	sporulation-specific N-acetylmuramoyl-L-alanine amidase	E5DV68	Deep-sea_thermophilic_phage	2.0e-51	49.1
WP_019258474.1\|1933937_1934906_+	stage V sporulation protein K	G3MAX6	Bacillus_virus	3.0e-52	40.5

DBSCAN-SWA_5

2195327 : 2207839

Bacillus_phage(90.0%)

holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_084995773.1\|2195327_2195555_-	helix-turn-helix transcriptional regulator	O64085	Bacillus_phage	8.9e-32	89.3
WP_084995771.1\|2195666_2196176_-	hypothetical protein	NA	NA	NA	NA
WP_084995769.1\|2196517_2196739_-	hypothetical protein	A0A0K2D0N5	Bacillus_phage	3.3e-07	42.4
WP_168767811.1\|2196756_2197188_-	hypothetical protein	NA	NA	NA	NA
WP_084995610.1\|2197697_2199209_-	S8 family serine peptidase	A0A217EQY2	Bacillus_phage	9.9e-18	32.7
WP_168767746.1\|2199686_2199836_-	hypothetical protein	NA	NA	NA	NA
WP_084995612.1\|2199956_2200331_+	hypothetical protein	A0A1P8CWZ2	Bacillus_phage	2.4e-26	48.8
WP_084995614.1\|2201128_2201278_+\|holin	phage holin	A0A1P8CWN5	Bacillus_phage	1.5e-19	97.9
WP_084995616.1\|2201405_2202542_+	RapH N-terminal domain-containing protein	A0A1P8CWN8	Bacillus_phage	7.1e-210	96.6
WP_019712878.1\|2202531_2202708_+	hypothetical protein	A0A1P8CWP3	Bacillus_phage	6.9e-24	98.3
WP_084995618.1\|2202749_2203388_-	DNA polymerase	A0A1P8CWP4	Bacillus_phage	2.2e-107	93.2
WP_084995620.1\|2203366_2203693_-	hypothetical protein	O64031	Bacillus_phage	6.6e-28	95.3
WP_084995622.1\|2203866_2204805_-	hypothetical protein	NA	NA	NA	NA
WP_084995624.1\|2204847_2205930_-	hypothetical protein	NA	NA	NA	NA
WP_084995626.1\|2205945_2206242_-	hypothetical protein	NA	NA	NA	NA
WP_084995628.1\|2206273_2207839_-	S8 family serine peptidase	A0A2K9L570	Tupanvirus	1.8e-06	29.6

DBSCAN-SWA_6

3388800 : 3396485

Organic_Lake_phycodnavirus(33.33%)

holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_084993408.1\|3388800_3389439_-\|holin	choline ABC transporter permease OpuBD	NA	NA	NA	NA
WP_084993409.1\|3389455_3390376_-	osmoprotectant ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_084993412.1\|3390387_3391041_-\|holin	choline ABC transporter permease OpuBB	NA	NA	NA	NA
WP_084993414.1\|3391055_3392201_-\|holin	betaine/proline/choline family ABC transporter ATP-binding protein	F2Y2R6	Organic_Lake_phycodnavirus	2.7e-15	32.7
WP_060399502.1\|3392485_3393019_+	GbsR/MarR family transcriptional regulator	NA	NA	NA	NA
WP_084993416.1\|3393052_3393721_-\|holin	glycine betaine/carnitine/choline/choline sulfate ABC transporter permease OpuCD	G3M9Y4	Bacillus_virus	7.3e-05	25.4
WP_084993418.1\|3393738_3394656_-	osmoprotectant ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_003235195.1\|3394669_3395323_-\|holin	glycine betaine/carnitine/choline/choline sulfate ABC transporter permease OpuCB	NA	NA	NA	NA
WP_084993420.1\|3395345_3396485_-\|holin	betaine/proline/choline family ABC transporter ATP-binding protein	W6JKT0	Anomala_cuprea_entomopoxvirus	3.6e-12	29.8

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP051462

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection