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
NZ_CP019637	Nostocales cyanobacterium HT-58-2 plasmid pHT582-1, complete sequence	0 crisprs	NA	0	0	0
NZ_CP019636	Nostocales cyanobacterium HT-58-2, complete genome	29 crisprs	cas14j,c2c9_V-U4,Cas14c_CAS-V-F,csa3,WYL,csx1,cas10,csm3gr7,csx10gr5,csx19,Cas14u_CAS-V,cas14k,cas6,2OG_CAS,csc1gr5,cas10d,csc2gr7,cas3,cas4,cas1,cas2,csx21,PD-DExK,csm2gr11,csx3,DinG,c2c10_CAS-V-U3	4	19	5
NZ_CP019638	Nostocales cyanobacterium HT-58-2 plasmid pHT582-2, complete sequence	0 crisprs	NA	0	0	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP019636_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_1

169080-169184

Orphan

Consensus_repeat	Method
ATTAGATTAGTAGTCAACTTCTGTGCTAAAGCACTACTAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_1

>merge|NZ_CP019636|1|169080-169184|CRISPRCasFinder
ATTAGATTAGTAGTCAACTTCTGTGCTAAAGCACTACTACTGGCGCGACACAGCTAAATTTGTGCATTAGATTAGTAGTCAACTTCTGTGCTAAAGCACTACTAC

>NZ_CP019636|1|1|169080-169184|CRISPRCasFinder
ATTAGATTAGTAGTCAACTTCTGTGCTAAAGCACTACTAC	TGGCGCGACACAGCTAAATTTGTGC
ATTAGATTAGTAGTCAACTTCTGTGCTAAAGCACTACTAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087537671.1\|167980_168841_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133016
NZ_CP019636.1\|WP_087545844.1\|165463_166528_-\|exostosin-family-protein	unknown	unknown	gnl\|CDD\|367297
NZ_CP019636.1\|WP_087537674.1\|171309_172143_-\|sulfite-exporter-TauE/SafE-family-protein	unknown	unknown	gnl\|CDD\|376667
NZ_CP019636.1\|WP_087545841.1\|162625_162811_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087537664.1\|160223_160610_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319940
NZ_CP019636.1\|WP_087537673.1\|170918_171308_-\|DUF1634-domain-containing-protein	unknown	unknown	gnl\|CDD\|377927
NZ_CP019636.1\|WP_087537679.1\|177704_178295_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087537678.1\|176095_177079_-\|RNA-polymerase-sigma-factor,-RpoD/SigA-family	unknown	unknown	gnl\|CDD\|180321
NZ_CP019636.1\|WP_087537667.1\|162005_162491_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087537665.1\|160888_161530_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274008
NZ_CP019636.1\|WP_087537676.1\|173525_174527_+\|putative-sulfate-exporter-family-transporter	unknown	unknown	gnl\|CDD\|225411
NZ_CP019636.1\|WP_087537670.1\|166651_167839_-\|deoxyhypusine-synthase	unknown	unknown	gnl\|CDD\|179117
NZ_CP019636.1\|WP_087537680.1\|178406_180137_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|223510
NZ_CP019636.1\|WP_087537675.1\|172456_173386_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176112
NZ_CP019636.1\|WP_087537677.1\|174713_175454_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087537672.1\|169747_170410_+\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	unknown	unknown	gnl\|CDD\|235662
NZ_CP019636.1\|WP_087537668.1\|162816_163893_-\|PIN/TRAM-domain-containing-protein	unknown	unknown	gnl\|CDD\|227292
NZ_CP019636.1\|WP_157679096.1\|169372_169726_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087537669.1\|164146_165331_+\|coproporphyrinogen-III-oxidase	unknown	unknown	gnl\|CDD\|236007
NZ_CP019636.1\|WP_087537666.1\|161556_162009_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087537671.1\|167980_168841_-\|glycosyltransferase	gnl\|CDD\|133016	cd02525, Succinoglycan_BP_ExoA, ExoA is involved in the biosynthesis of succinoglycan. Succinoglycan Biosynthesis Protein ExoA catalyzes the formation of a beta-1,3 linkage of the second sugar (glucose) of the succinoglycan with the galactose on the lipid carrie. Succinoglycan is an acidic exopolysaccharide that is important for invasion of the nodules. Succinoglycan is a high-molecular-weight polymer composed of repeating octasaccharide units. These units are synthesized on membrane-bound isoprenoid lipid carriers, beginning with galactose followed by seven glucose molecules, and modified by the addition of acetate, succinate, and pyruvate. ExoA is a membrane protein with a transmembrance domain at c-terminus.	3.76955e-34
NZ_CP019636.1\|WP_087545844.1\|165463_166528_-\|exostosin-family-protein	gnl\|CDD\|367297	pfam03016, Exostosin, Exostosin family. The EXT family is a family of tumor suppressor genes. Mutations of EXT1 on 8q24.1, EXT2 on 11p11-13, and EXT3 on 19p have been associated with the autosomal dominant disorder known as hereditary multiple exostoses (HME). This is the most common known skeletal dysplasia. The chromosomal locations of other EXT genes suggest association with other forms of neoplasia. EXT1 and EXT2 have both been shown to encode a heparan sulphate polymerase with both D-glucuronyl (GlcA) and N-acetyl-D-glucosaminoglycan (GlcNAC) transferase activities. The nature of the defect in heparan sulphate biosynthesis in HME is unclear.	7.74734e-08
NZ_CP019636.1\|WP_087537674.1\|171309_172143_-\|sulfite-exporter-TauE/SafE-family-protein	gnl\|CDD\|376667	pfam01925, TauE, Sulfite exporter TauE/SafE. This is a family of integral membrane proteins where the alignment appears to contain two duplicated modules of three transmembrane helices. The proteins are involved in the transport of anions across the cytoplasmic membrane during taurine metabolism as an exporter of sulfoacetate. This family used to be known as DUF81.	1.40644e-27
NZ_CP019636.1\|WP_087537664.1\|160223_160610_+\|VOC-family-protein	gnl\|CDD\|319940	cd08352, VOC_Bs_YwkD_like, vicinal oxygen chelate (VOC) family protein Bacillus subtilis YwkD and similar proteins. uncharacterized subfamily of vicinal oxygen chelate (VOC) family contains Bacillus subtilis YwkD and similar proteins. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	4.1601e-77
NZ_CP019636.1\|WP_087537673.1\|170918_171308_-\|DUF1634-domain-containing-protein	gnl\|CDD\|377927	pfam07843, DUF1634, Protein of unknown function (DUF1634). This family contains many hypothetical bacterial and archaeal proteins. A few members of this family are annotated as being putative transmembrane proteins, and the region in question in fact contains many hydrophobic residues.	1.07257e-30
NZ_CP019636.1\|WP_087537678.1\|176095_177079_-\|RNA-polymerase-sigma-factor,-RpoD/SigA-family	gnl\|CDD\|180321	PRK05949, PRK05949, RNA polymerase sigma factor; Validated.	0
NZ_CP019636.1\|WP_087537665.1\|160888_161530_+\|hypothetical-protein	gnl\|CDD\|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	0.00144157
NZ_CP019636.1\|WP_087537676.1\|173525_174527_+\|putative-sulfate-exporter-family-transporter	gnl\|CDD\|225411	COG2855, COG2855, Predicted membrane protein [Function unknown].	5.45394e-55
NZ_CP019636.1\|WP_087537680.1\|178406_180137_-\|ATP-binding-protein	gnl\|CDD\|223510	COG0433, COG0433, HerA helicase [Replication, recombination, and repair].	1.89716e-57
NZ_CP019636.1\|WP_087537675.1\|172456_173386_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|176112	cd08420, PBP2_CysL_like, C-terminal substrate binding domain of LysR-type transcriptional regulator CysL, which activates the transcription of the cysJI operon encoding sulfite reductase, contains the type 2 periplasmic binding fold. CysL, also known as YwfK, is a regular of sulfur metabolism in Bacillus subtilis. Sulfur is required for the synthesis of proteins and essential cofactors in all living organism. Sulfur can be assimilated either from inorganic sources (sulfate and thiosulfate), or from organic sources (sulfate esters, sulfamates, and sulfonates). CysL activates the transcription of the cysJI operon encoding sulfite reductase, which reduces sulfite to sulfide. Both cysL mutant and cysJI mutant are unable to grow using sulfate or sulfite as the sulfur source. Like other LysR-type regulators, CysL also negatively regulates its own transcription. In Escherichia coli, three LysR-type activators are involved in the regulation of sulfur metabolism: CysB, Cbl and MetR. The topology of this substrate-binding domain 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.	2.16485e-69
NZ_CP019636.1\|WP_087537672.1\|169747_170410_+\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	gnl\|CDD\|235662	PRK05986, PRK05986, cob(I)yrinic acid a,c-diamide adenosyltransferase.	1.10407e-104
NZ_CP019636.1\|WP_087537668.1\|162816_163893_-\|PIN/TRAM-domain-containing-protein	gnl\|CDD\|227292	COG4956, COG4956, Integral membrane protein (PIN domain superfamily) [General function prediction only].	3.53791e-167
NZ_CP019636.1\|WP_087537669.1\|164146_165331_+\|coproporphyrinogen-III-oxidase	gnl\|CDD\|236007	PRK07379, PRK07379, coproporphyrinogen III oxidase; Provisional.	0
NZ_CP019636.1\|WP_087537670.1\|166651_167839_-\|deoxyhypusine-synthase	gnl\|CDD\|179117	PRK00770, PRK00770, deoxyhypusine synthase.	0

>NZ_CP019636.1|WP_087537671.1|167980_168841_-|glycosyltransferase
MKLSVVIPCFNAADTIAFQLEALARQQCSQPWEIIVADNGSTDDTVAIIKQYQQRIPHLRFVEASARRGSAHARNVGVSVAKSEAIAFCDADDEVAPGWVAAMIEALSKYDLVAGRNEYSKLNQLWVIQCCEYREGNGVNQHPYFPYAGCSNLGVKRSVHEMVGGFDETMLSLQDVDYCWRIQEAGKTLDSAKDALVHFRFRNTTRGLYHRYWKLACYDVLLHKKHQQVGMPKLIKWQGFVKDGVILPVKFIVKVRNRESLVRWLLDFAWLAGHLQGCIKYKYLPL
>NZ_CP019636.1|WP_087537670.1|166651_167839_-|deoxyhypusine-synthase
MSKHLEKKIAPAPIPTDIGVVDLIDNYFTAYNSARLREICHLLSRDVFIEGVTVGVSLSGALTPAGFGVSALTPLIRNGFIDWIISTGANLYHDMHYGLGFELFTGHPFLDDVKLRQQGTIRIYDIIFGYDVLLETDAFIRKILQAEPFQKRMGTAEFHNLLGKYVREVEKQLGVKHSSLLATAYEYGVPIYTSSPGDSSIGMNVAALSLEGSQLVLDPAIDVNETAAIAYSARETGGKSAAVILGGGSPKNFLLQTQPQIHEVLGLEERGHDYFIQFTDARPDTGGLSGATPSEAVSWGKIDPDELPSTIVCYTDSTIALPLLTAYVLNQCQPRTLKRVYDRREQMLDKLRTDYLAAKTQPVDEIPAAMTEGIPPHKVATYPVGRLISHTGGAE
>NZ_CP019636.1|WP_087545844.1|165463_166528_-|exostosin-family-protein
MKPLSNQYFVYIKADQEPIPWNIYDVNPPSNLGLSTYYSRVFQAMEKHLKVSGLVFYVTWDEINELPSYGENVIAVVLGDEWFRIPKYFHKVGAVFKCLGTRPILGCNPLLQPSYLNFLSVIQFLRILVYRLPWVINYHFQKFKLWQTGRTEIPPIYDIPQGYGNSKDLPIKDIEARPNDVFFAGSVVHVPLPPWSLKQWLGTPKTFSRREMISSLNNFMEKHPEMKADLSVTPGFHATSQEDVSTYSERMMNAKICLIPRGTSFETIRFFEAIRYGCIPVTELLPSRWFYEEAPAIQIKNWRELGEVLENLLENKHLLQEKHQESLKWWETKCSEAVVGQYMAERLNSLKSAS
>NZ_CP019636.1|WP_087537669.1|164146_165331_+|coproporphyrinogen-III-oxidase
MIQNISTFGIPSSAYIHIPFCRRRCFYCDFPVSVVGERLRGETSGTISQYVHMLCQEIAITPALGQPLITIFFGGGTPSLLSTEQLKSILAALEAQFGVSPGAEISMEIDPGTFDLGHLQGYRSAGVNRISLGVQAFQEDLLQICGRSHSVSDIFAAVDLIQQAKIPEFSLDLISGLPHQTLDRWQESLEKAVTIAPTHISIYDLTIEPGTAFGRYYKPGDQPLPTDETTVKMYRMAQQILTSAGYEHYEISNYAKPGHQCRHNRVYWENRPYYGFGMGAASYVEGKRFTRPRKTKEYYQWMQDGSVIDCEVTSPEEALLETLMLGLRLAEGVSLAVLAKQFGEEKVEEIHKCLQPYFEKGWVEIVEERLHLSDPDGFLFSNVVLARLFSELGK
>NZ_CP019636.1|WP_087537668.1|162816_163893_-|PIN/TRAM-domain-containing-protein
MLDAIIIFSFVLAAAGIGYYSTDLLPTGALARVSNLEALRMVVAAFAAMFGGALGLSFQTGYRRLQAQVRELPLEVILTRAIGLVIGLLIANLMLAPLFLLPIPADFSFIKPLVAVVGSIILSYTGMNLADAHGRGLLRLINPNTVESMVVEGTLKPASTKVLDTSCIIDGRIETLLETGFLEGQIIVPQFVLQELQQVADASKDQKRVRGRRGLEILNRIKAAYPDRILINSIDYDDIATVDAKLVRFAQEINATLLTNDYNLSKVASVQKVPVLNVNDLVNAVRPTYLPGDNIDLKILKEGKEPSQGIGYLDDGTMVVVEEGSNYVGGELRVVVTSALQTSAGRMIFAKPQASAIA
>NZ_CP019636.1|WP_087545841.1|162625_162811_-|hypothetical-protein
MARSIRVKLCDRCRLTAPILYRVKYQEDGEWIFVCLECWQQVSENNPFYVYGGTWKAQKKR
>NZ_CP019636.1|WP_087537667.1|162005_162491_+|hypothetical-protein
MKSLSQLIKELEQIKKRSDVAINAIEDINQQWEKECSPRALYRHLKASGIYEQWIQEQIKVQNNRCFNKKCRCLFSDDNPFTVDHVEPLSPRKIPENPDKLWGYTSNTTNNFILLCITCNKLKSNHTDIDIWMGWNRADIERLRQNSQRRVGSTEAPEDIP
>NZ_CP019636.1|WP_087537666.1|161556_162009_+|hypothetical-protein
MKTITRKQLKTFGCSDYLARKLTNGVMYTKDKRERGYICQGVAKKIDDTLNNTSRIQYKTVQILEDLLRKIKSFSPEVWVEILESEEMAQVVDEIKNFNKHYPEICKRSDQAIQAISEALEEHSKAMQEYLKHLSPKTQKEFLQSIEGAV
>NZ_CP019636.1|WP_087537665.1|160888_161530_+|hypothetical-protein
MAEEPKLLIKLDAQRKKILRVYLGWTLADVERAISNQPSLTVDDVLKVFSQEEWNELSLKLASFAGPETKSRQRQQAYQKGLVTQRNKDITRLEEEMSALQEQIRKDRKQIEINQKEIGEQQKTIEKQEKAIAGQKQEIERQEKEIEVQQKFLNKNAIVIKKLQESGKILKDENIYLREISESQQTALKKIRDFIISKIKYIPLEIKKFLDIS
>NZ_CP019636.1|WP_087537664.1|160223_160610_+|VOC-family-protein
MKTTGIHHVAIICSDYERSKKFYTEILGFSILKETFRAQRNSYKLDLQVGDNHQIELFSFPNPPQRLSHPEACGLRHLAFEVDNIEQTVNDLKSQGIEVEDIRIDEITGKKFTFFQDPDNLPLEIYER
>NZ_CP019636.1|WP_157679096.1|169372_169726_-|hypothetical-protein
MTALRTLGRGFLDQWESSDFTLTKIHCDAPHRCMDRENSFCSPGAKTFSGDYAHCETGSSAAARDSGCVASHSIVSKVALEGRGLYPIFLVINTRMNQNTPDRATGFNEKQNFYEPK
>NZ_CP019636.1|WP_087537672.1|169747_170410_+|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase
MQTDETWATTSDVTVRENSSLTSEQYRKKMQRRQEVQEARMTHASSEKGLIIVNTGHGKGKTTAALGMVLRALGHGYKVAIVQFIKGAWEPAEKRVFSIWQDDLLEFHAMGEGFTWDTQDRDRDIEKAIAAWQKGLEYIRNPDFKLVLLDEINIALKLGYLQVEEVLAGLAQKPHDNHVILTGRGAPTALIERADLVTEMTLVKHPLRDQGIKAQPGIEY
>NZ_CP019636.1|WP_087537673.1|170918_171308_-|DUF1634-domain-containing-protein
MSQPRRRWSEHQIEQFVGNLLRLGVVFATSVVLIGGVLYLIRYGCSSTNYQFFRGEPADFRSPEGVATAVLLGRRRGVIQLGLLLLIATPIARVVFSLFAFVRQRDLTYTIITLIVLTGLVYSLLSGNS
>NZ_CP019636.1|WP_087537674.1|171309_172143_-|sulfite-exporter-TauE/SafE-family-protein
MNILEFSLSVWLGSLTAGFLGSLTGLGGGVVIVPLLTLAFGVDIRYAVGASLVSVIATSSGAASAYVKEGYTNLRLGMFLEVATTFGAIVGAIVAGIVSTRAIAIVFGIVLLYSAYLSRQHRIEHLDSEPDPLATLLKLNGSYPTPDGQKFYTVRAVPVGFGLMFLAGVLSGLLGIGSGAVKVLAMDQAMRIPFKVSTTTSNFMIGVTAAASAGVYLKRGYIDPGLAMPVMLGVLFGALLGARVLVRARIGLLRNIFSLVILGLAVEMIYKGLTGGI
>NZ_CP019636.1|WP_087537675.1|172456_173386_-|LysR-family-transcriptional-regulator
MTRMTLDQLEIFLAVAQHMHFTRAAEALYITQSSVSAAIQSLEEKYGVKLFHRIGRHIEITDAGMLLQVEAQKIFNAVALCERGLRELNNLQQGELRLGASQTIGNYWLPQFISKFKQQYSGIQVNCTLGNTQEISAGTVKGLFDLGLVEGEIEPSVKDFLEQRVVGGDRLLVVVGKSHPWFERQSVSMYELSKTVWVMREKGSGTRQRFEQALQDWGIELAELTVILEMSTGEMVKVAVESGVGVAAISELMVNKELQLGTLRAVVIIDGAQKSTTFFDITRQFVLLKHRERFSTRVSQAFEQILITH
>NZ_CP019636.1|WP_087537676.1|173525_174527_+|putative-sulfate-exporter-family-transporter
MKKISSPDYPIRLEKRISVGVRKLLFLCSAFLCLINWISSPLALTLGMILSLTVQNPFPRTSRYVAKYLLQGCVILLGFGMNLAVVLKAGESGALFAAVSIVATFFCGNILGQQLKIPVKASVLISAGTAICGGSAIAAVSSVISAAESEISVAMGTVFLLNAVALYVFPPLGHLLHLTPTQFGTWAGVAIHDISSVVGAASHFGLGALSTATAVKLSRALWIVPVSVTAAFIFRRYHIWDKQQIPNPIQIPWFIGLFLLASVVRTFVPGTAIWSPLLTRLSESGLTLTLFLIGAGLSQPALKAVGWKPMVQGMVLWVFISVSSMLIIRQVVH
>NZ_CP019636.1|WP_087537677.1|174713_175454_-|hypothetical-protein
MPNNIKKFPSSSLLGIPFVGVLLLLGVVANRPKPVMSNQLAYVDSSIVSSTDSQLPTYTWLQRNPYPTSEYTQNKETRLQRVLAKSATVPTHFTHPNNLEAVSTTTTKVGDPLTSAQTTATTPIRARLPKQDGIYLYGQSPKSGQLGQGYIIFEKQQGKVVGALYMPSSEFSCFNGTLHSSGELAMTVTGYPGDKSPTQVATNNTLPRVMDDESSTYAHSVTLQDYYSLNNISAIDRRILQMCQSK
>NZ_CP019636.1|WP_087537678.1|176095_177079_-|RNA-polymerase-sigma-factor,-RpoD/SigA-family
MPTVDNQTENLNAKFTADMVRTYLREIGRVPLLTREQEIVYGKQVQQMMTLLDAKEALAKKLRHEPTLQEWADHVRKSETDVKQIVHQGKRAKQKMIEANLRLVVAIAKKYQKRNMEFLDLIQEGTLGLERGVEKFDPMRGYKFSTYAYWWIRQAITRAIAQQGRTIRLPIHITEKLNKIKKVQRELAQTLGRSPSPAEIAKELELEPAQIREYLNMARQPVSLDVKVGDNQDTELQEMLEDEGPSPEYYMTQEFLRQDLNNMLAELTPQQREVLALRFGLVDGNEMSLAKVGERLNLSRERVRQLEHQALAHLRRRRANVKEYVAS
>NZ_CP019636.1|WP_087537679.1|177704_178295_-|hypothetical-protein
MSSTLNPLSNDPLLAAVVDELCNIHGCHTVILYRSRAKGTHTAESDYELFAVRQTGESLHNARLWNNSYLDIFIYNEKDVIIIDSSFLRIRGGIVLREQESFAQRLLKQVDEFFATSPAVLSANEIQRRHTWFSKMLKRISQGDIEADHRRVWLLYALLEDYFALSQKWYLGSKESWKWLKIHDPGTYKAIDVQGN
>NZ_CP019636.1|WP_087537680.1|178406_180137_-|ATP-binding-protein
MNLGQPLGSVIQGSLTGGLEVRLHPDVSVEDMRVGKFLVVQGVRSRFFCMLTDVALGIANQRIIANPPNWEDTFLREILAGGGTYGTINLAPMLMFTPESEETYSPTNGKSANPFVPSTTGLASFQPQTNTTMELLPVKTIPSHFSQVYEASEEDFRRVFGWEDDPQRKNFSIGKPLDMEVPVCLDLNRFVERSNGVFGKSGTGKSFLTRLLLAGTIRKNAAVNLIFDMHSEYGWEAVSEGKQMSTVKGLKQLFPSLVEVYTLDPESTKRRGVPHAQELYLSYDQIEVEDIKLCSRDLGLSEASLDNANILYAEFGKSWILQLINMTNEEIKLFCEEKRGHQGSITALQRKLLRLENLKYMRAACPQNYVNQMLRSLEAGKNIVVEFGSQSNMLSYMLVTNMITRRIHQHYVSKAEKFLQTKNPTDRPTQLMITIEEAHRFLDPATVQSTIFGTIAREMRKYFVTLLVVDQRPSGIDNEVMSQIGTRITALLNDEKDIEAIFTGVSGGGALRSVLAKLDSKQQALILGHAVPMPVVVRTRPYDTKFYEEIGETAWDEKPDEEVFAAAELAKADLGF

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Crispr_ID: NZ_CP019636_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_2

1030714-1030828

Orphan

Consensus_repeat	Method
AAAATACGTAGGATGTGTTAGCGCTAGCGTAACGCATCATTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_2

>merge|NZ_CP019636|2|1030714-1030828|CRISPRCasFinder
AAAATACGTAGGATGTGTTAGCGCTAGCGTAACGCATCATTCTTCTGCATAAAATGGATAATATTTGATTTTGAAAATATGTAGGATGTGTTAGCGCTAGCGTAACGCATCATTC

>NZ_CP019636|2|2|1030714-1030828|CRISPRCasFinder
AAAATACGTAGGATGTGTTAGCGCTAGCGTAACGCATCATTC	TTCTGCATAAAATGGATAATATTTGATTTTG
AAAATATGTAGGATGTGTTAGCGCTAGCGTAACGCATCATTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087538271.1\|1016319_1019895_-\|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase	unknown	unknown	gnl\|CDD\|131231
NZ_CP019636.1\|WP_087538279.1\|1031397_1031943_-\|oxidoreductase	unknown	unknown	gnl\|CDD\|224852
NZ_CP019636.1\|WP_087538278.1\|1030906_1031326_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538274.1\|1027414_1027672_-\|HypC/HybG/HupF-family-hydrogenase-formation-chaperone	unknown	unknown	gnl\|CDD\|376549
NZ_CP019636.1\|WP_087538287.1\|1044068_1046516_-\|phosphoenolpyruvate-synthase	unknown	unknown	gnl\|CDD\|235809
NZ_CP019636.1\|WP_087538275.1\|1027712_1028054_-\|hydrogenase-maturation-nickel-metallochaperone-HypA	unknown	unknown	gnl\|CDD\|376468
NZ_CP019636.1\|WP_087538273.1\|1023251_1026557_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|237425
NZ_CP019636.1\|WP_087538276.1\|1028035_1028527_-\|hydrogenase-maturation-protease	unknown	unknown	gnl\|CDD\|99876
NZ_CP019636.1\|WP_087538277.1\|1028706_1029165_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225222
NZ_CP019636.1\|WP_087538272.1\|1020088_1022509_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|237425
NZ_CP019636.1\|WP_087538286.1\|1041131_1043924_-\|bifunctional-acetate--CoA-ligase-family-protein/GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|223972
NZ_CP019636.1\|WP_087538280.1\|1032005_1032530_-\|DUF3122-domain-containing-protein	unknown	unknown	gnl\|CDD\|371466
NZ_CP019636.1\|WP_087538283.1\|1034988_1035528_-\|bidirectional-hydrogenase-complex-protein-HoxE	unknown	unknown	gnl\|CDD\|236053
NZ_CP019636.1\|WP_087538281.1\|1032566_1033283_-\|bidirectional-hydrogenase-complex-protein-HoxU	unknown	unknown	gnl\|CDD\|181037
NZ_CP019636.1\|WP_087538284.1\|1035844_1038361_-\|magnesium-translocating-P-type-ATPase	unknown	unknown	gnl\|CDD\|319772
NZ_CP019636.1\|WP_087538285.1\|1038412_1041025_-\|HAD-IC-family-P-type-ATPase	unknown	unknown	gnl\|CDD\|319839
NZ_CP019636.1\|WP_087545984.1\|1029232_1030681_-\|Ni/Fe-hydrogenase-subunit-alpha	unknown	unknown	gnl\|CDD\|225798
NZ_CP019636.1\|WP_087538269.1\|1014089_1015190_-\|hydrogenase-formation-protein-HypD	unknown	unknown	gnl\|CDD\|237892
NZ_CP019636.1\|WP_087538282.1\|1033300_1034905_-\|NADH-quinone-oxidoreductase-subunit-L	unknown	unknown	gnl\|CDD\|224806
NZ_CP019636.1\|WP_087538270.1\|1015270_1016302_-\|dihydroorotate-dehydrogenase-like-protein	unknown	unknown	gnl\|CDD\|236051

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087538271.1\|1016319_1019895_-\|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase	gnl\|CDD\|131231	TIGR02176, pyruvate_flavodoxin/ferrodoxin_oxidoreductase, pyruvate:ferredoxin (flavodoxin) oxidoreductase, homodimeric. This model represents a single chain form of pyruvate:ferredoxin (or flavodoxin) oxidoreductase. This enzyme may transfer electrons to nitrogenase in nitrogen-fixing species. Portions of this protein are homologous to gamma subunit of the four subunit pyruvate:ferredoxin (flavodoxin) oxidoreductase.	0
NZ_CP019636.1\|WP_087538275.1\|1027712_1028054_-\|hydrogenase-maturation-nickel-metallochaperone-HypA	gnl\|CDD\|376468	pfam01155, HypA, Hydrogenase/urease nickel incorporation, metallochaperone, hypA. HypA is a metallochaperone that binds nickel to bring it safely to its target. The targets for Hypa are the nickel-containing enzymes [Ni,Fe]-hydrogenase and urease. The nickel coordinates with four nitrogens within the protein. The four conserved cysteines towards the C-terminus bind one zinc moiety probably to stabilize the protein fold.	3.81128e-36
NZ_CP019636.1\|WP_087538274.1\|1027414_1027672_-\|HypC/HybG/HupF-family-hydrogenase-formation-chaperone	gnl\|CDD\|376549	pfam01455, HupF_HypC, HupF/HypC family.	1.51978e-31
NZ_CP019636.1\|WP_087538287.1\|1044068_1046516_-\|phosphoenolpyruvate-synthase	gnl\|CDD\|235809	PRK06464, PRK06464, phosphoenolpyruvate synthase; Validated.	0
NZ_CP019636.1\|WP_087538279.1\|1031397_1031943_-\|oxidoreductase	gnl\|CDD\|224852	COG1941, FrhG, Coenzyme F420-reducing hydrogenase, gamma subunit [Energy production and conversion].	8.10826e-67
NZ_CP019636.1\|WP_087538273.1\|1023251_1026557_-\|PAS-domain-S-box-protein	gnl\|CDD\|237425	PRK13557, PRK13557, histidine kinase; Provisional.	1.37927e-74
NZ_CP019636.1\|WP_087538276.1\|1028035_1028527_-\|hydrogenase-maturation-protease	gnl\|CDD\|99876	cd06066, H2MP_NAD-link-bidir, Endopeptidases that belong to the bidirectional NAD-linked hydrogenase group. This group of endopeptidases are highly specific carboxyl-terminal protease (HoxW protease) which releases a 24-amino-acid peptide from HoxH prior to progression of subunit assembly. These bidirectional hydrogenases are heteropentamers encoded by the hox (hydrogen oxidation) genes, in which complex HoxEFU shows the diaphorase activity, and HoxYH constitutes the NiFe-hydrogenase.	2.60169e-52
NZ_CP019636.1\|WP_087538277.1\|1028706_1029165_-\|hypothetical-protein	gnl\|CDD\|225222	COG2345, COG2345, Predicted transcriptional regulator [Transcription].	0.0080951
NZ_CP019636.1\|WP_087538272.1\|1020088_1022509_-\|PAS-domain-S-box-protein	gnl\|CDD\|237425	PRK13557, PRK13557, histidine kinase; Provisional.	6.07873e-71
NZ_CP019636.1\|WP_087538286.1\|1041131_1043924_-\|bifunctional-acetate--CoA-ligase-family-protein/GNAT-family-N-acetyltransferase	gnl\|CDD\|223972	COG1042, COG1042, Acyl-CoA synthetase (NDP forming) [Energy production and conversion].	0
NZ_CP019636.1\|WP_087538280.1\|1032005_1032530_-\|DUF3122-domain-containing-protein	gnl\|CDD\|371466	pfam11320, DUF3122, Protein of unknown function (DUF3122). This family of proteins with unknown function appear to be restricted to Cyanobacteria.	9.81588e-58
NZ_CP019636.1\|WP_087538283.1\|1034988_1035528_-\|bidirectional-hydrogenase-complex-protein-HoxE	gnl\|CDD\|236053	PRK07571, PRK07571, bidirectional hydrogenase complex protein HoxE; Reviewed.	5.52088e-103
NZ_CP019636.1\|WP_087538281.1\|1032566_1033283_-\|bidirectional-hydrogenase-complex-protein-HoxU	gnl\|CDD\|181037	PRK07569, PRK07569, bidirectional hydrogenase complex protein HoxU; Validated.	7.7791e-172
NZ_CP019636.1\|WP_087538284.1\|1035844_1038361_-\|magnesium-translocating-P-type-ATPase	gnl\|CDD\|319772	cd02077, P-type_ATPase_Mg, magnesium transporting ATPase (MgtA), similar to Escherichia coli MgtA and Salmonella typhimurium MgtA. MgtA is a membrane protein which actively transports Mg(2+) into the cytosol with its electro-chemical gradient rather than against the gradient as other cation transporters do. It may act both as a transporter and as a sensor for Mg(2+). In Salmonella typhimurium and Escherichia coli, the two-component system PhoQ/PhoP regulates the transcription of the mgtA gene by sensing Mg(2+) concentrations in the periplasm. MgtA is activated by cardiolipin and it highly sensitive to free magnesium in vitro. It consists of a transmembrane domain and three cytosolic domains: nucleotide-binding domain, phosphorylation domain and actuator domain, and belongs to the P-type ATPase type III subfamily. The P-type ATPases, are a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_CP019636.1\|WP_087538285.1\|1038412_1041025_-\|HAD-IC-family-P-type-ATPase	gnl\|CDD\|319839	cd07538, P-type_ATPase, uncharacterized subfamily of P-type ATPase transporters. This subfamily contains P-type ATPase transporters of unknown function. The P-type ATPases, are a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids. They are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle. A general characteristic of P-type ATPases is a bundle of transmembrane helices which make up the transport path, and three domains on the cytoplasmic side of the membrane. Members include pumps that transport various light metal ions, such as H(+), Na(+), K(+), Ca(2+), and Mg(2+), pumps that transport indispensable trace elements, such as Zn(2+) and Cu(2+), pumps that remove toxic heavy metal ions, such as Cd2+, and pumps such as aminophospholipid translocases which transport phosphatidylserine and phosphatidylethanolamine.	0
NZ_CP019636.1\|WP_087545984.1\|1029232_1030681_-\|Ni/Fe-hydrogenase-subunit-alpha	gnl\|CDD\|225798	COG3259, FrhA, Coenzyme F420-reducing hydrogenase, alpha subunit [Energy production and conversion].	0
NZ_CP019636.1\|WP_087538269.1\|1014089_1015190_-\|hydrogenase-formation-protein-HypD	gnl\|CDD\|237892	PRK15062, PRK15062, hydrogenase isoenzymes formation protein HypD; Provisional.	0
NZ_CP019636.1\|WP_087538282.1\|1033300_1034905_-\|NADH-quinone-oxidoreductase-subunit-L	gnl\|CDD\|224806	COG1894, NuoF, NADH:ubiquinone oxidoreductase, NADH-binding (51 kD) subunit [Energy production and conversion].	0
NZ_CP019636.1\|WP_087538270.1\|1015270_1016302_-\|dihydroorotate-dehydrogenase-like-protein	gnl\|CDD\|236051	PRK07565, PRK07565, dihydroorotate dehydrogenase-like protein.	0

>NZ_CP019636.1|WP_087545984.1|1029232_1030681_-|Ni/Fe-hydrogenase-subunit-alpha
MKKIIIDPVTRIEGHAKITIYLDDAGQVSDARFHVTEFRGFEKFCEGRPLWEMPGITARICGICPVSHLLASAKAGDRILAVTIPKAAKKLRRLMNLGQIIQSHALSFFHLSAPDLLLGMDSNSQKRNVFGLIAAEPELARGGIRLRQFGQEIIEQLGGQKIHPAWAVPGGVREPLSQEGRTHIQNRIPEVRTTILDALGRFKRLLKDYEKEAQTFGNFPSLFMGLVTPEGLWENYDGHIRFVDSAGNIIADKLDPTHYQEFIGEAVQPDSYLKSPYYRPLGYPDQSNHCRLDSGIYRVGPLARLNICSHIGTPLADLELREFRDRGKGTVTSSFFYHYARLIEILASIERIEILLDDSDLLSNRLRADAGINQLEGVGVSEAPRGTLFHHYQVDENGLIQKVNLVIATGQNNLAMNRTVAQIARHFIHGSEISEGMLNRVEAGIRAFDPCLSCSTHAAGQMPLHIQLVSVDGSVVNELWRE
>NZ_CP019636.1|WP_087538277.1|1028706_1029165_-|hypothetical-protein
MITKEAAQRLRQRFERFSELKAEYGTSKALEIMRSGQAELQKKLMEPLINQVSLAEGFRQSISIFEEFGMNMEVVDISNVGKDAVLEIQRVCPYMSLAREFGLQTPCQITCDMEVEAVEEAFPDMKGRILSKLACGDCVCVFKYERDTNSRN
>NZ_CP019636.1|WP_087538276.1|1028035_1028527_-|hydrogenase-maturation-protease
MENVMINTCPTILLIGYGNELRSDDAVGQRVSDLIASWKLTNLSTLCVRQLTPELAELLTKFDVAIFVDAYLATMEQDVQVCPIELTDSSITMGHSSNPSYLLTLTKALYGHSLQAWWVIVPGMNFELGESLSPTAEQGIEIALQKINQLIKTIRKEICMKLE
>NZ_CP019636.1|WP_087538275.1|1027712_1028054_-|hydrogenase-maturation-nickel-metallochaperone-HypA
MHEVGMMQNIIDAAVKRAKDEGAQHIRLVQMRVGEVSGVVADSLQLAFEVTKKGTIAEDARLQVENVPVVCYCSNCNIEFHPNSELNECPECHQSYCEVRQGKEFELAFLEVS
>NZ_CP019636.1|WP_087538274.1|1027414_1027672_-|HypC/HybG/HupF-family-hydrogenase-formation-chaperone
MCLAVPGKIISINGEDSLMRTGKVSFGGIIKEVCMAYVPDAKVDDYVIVHIGFAISILDPQEAQYTIDAWRLLNAEYSTAEQYEQ
>NZ_CP019636.1|WP_087538273.1|1023251_1026557_-|PAS-domain-S-box-protein
MPSIYPVDLPTIEQVMESYPLTVLPNTLLVDVIALMNPVNSSTVDSASDFSSCVLVVEENTLVGIFTLRDVVRLTGAGVDLFRVKISEVMTQPVISLTRAAAQNALTALAFMRQHHIRHLPVVNEQGQLLGLITQDRIRQVIQPAHLLKLRCVTEVMVREVIHALPTISVLELSQMMSDRRISCVVIVAPQETKLIPVGMITEKDILKVQLQGLDMAQTQVQAVMSTPVLSINPSESLLTVHQLMQEQGVRRVAVVDEQGELQGLVTQTNLLQVLDPLEIVSIIQALQTKVEEQTVQLRQTNQQLEQEVRQRRQVEESLCQAQQELELRVLERTDGLVQANARLQAEIEERTKAETELQLTKFCIDRATDASACIDLNGRYVYVNDTMCHTLNYSREELLLMSVYDINVDISTPAVWADFWQKLKQQGFMVFESHHRRRDGQINPVEITTNYFKFQGQEFLWGFARNITGRKQAEAALRASQQQLQAIIDNSPAVIYVKDVQGQHILVNSEFERITHLTREQVKNKTDYELFSPDIAQALSRNDQNVLTSLTPLQFEEEVELDDRLHTYITVKFPLCDADGQPYGICGISTDITARKQAQQQIREQAVLIDIATDAFVVRDLENRILFWSQGAERLYGWTAEESLGKKTHELFHTQPLSQVEAALKTTVEQGFWEGEFNKTTKNGSNIIVASRWTLVHNQFGQTQSILVVDTDITDKKQLEQQFYRAQRLESVGTLASGIAHDLNNVFAPIMMIAQLLTSRCKNVDARTQELFKTLENSSKRGADLVKQILTFARGTEGKQILLQPGHLLKELVKVIQQTFPKSIEIVTDIPTNTLWMVQADPTQLDQVFMNLAVNARDAMPNGGRLIITAENRIIDETYARMHLEAEAGDYIVVTISDTGTGIPPEILERIFDPFFTTKEVGKGTGLGLSTVLGIVKNHGGFVEVASQVSQGTQFQVFLPRGEGTATKATAKTELPRGNGELILVVDDEKIVHQTTQETLTDYDYKTLVANDGIEAIALYVEYQPEISAVLLDMLMPNMDGLTAIRTLRTINPNVKIVATSGLHANEQKAIAAGADKFLSKPYTTTDLLTTLSDVIGVKK
>NZ_CP019636.1|WP_087538272.1|1020088_1022509_-|PAS-domain-S-box-protein
MSENDGFKNITACQQAYEVLQQAYEDLERRVEERTAELFHFNQLLQQEISDRKQAEAQIAFQASVLNQVRNAVIATDLEGKITYWNQFAQQLYELTPDVMSRSIMEVTVPPNQIEAAQEIMACIQEKGYWEGEFIVRRQDSSTFVASVVNALIYDTEGNPSGFVGVSMDISDRKAAEEALRQSEELYRNLIESQTDLIVRIDMQGRLTFANTVACETFGFQRNEFLGQSLLQVVHPEDLPDVMANMQALTSPPYRLTTKEQRELTVIGMRWFQWEIAAIRNQQGQVIELQGVGRDVTERKQAEEKIREQATLLNVASDAIIVRDLKHQIFFWNQGAQHLYGWQSAEVVGKKATELFSDKILPDVELALKTTIEQGKWEGELQHKTKDGRKVIVQSRWTLVRDNTGQPKFFLTVNTDITEKKQLEAQFLRTQRLESLGTLASGIAHDLNNILSPILVIAQLLSAKFPNLDKQNRELLEILENNSKRAVELVKQILSFAGGTEGKHIPLQLRHLLKDIRQIVISTFPKSIEVNITNIPTQNLWTVCADPIQVHQVLMNLCVNARDAMPKGGTLSICADNFCVDENYARMNLEAKVGNYVVITVSDTGCGIPQQTIERIFEPFFTTKEPGKGTGLGLSTVIGIVKNHSGFVEVYSEVGKGSQFKVYLSASDRQVTQNASTSEMPTGNGELILVVDNEASILEATKTSLETLNYKILTANDAVEAFSLYTRHKNQISVVLMDIQMPSLDGLNAIRILQKMNPSIKIIAISGLASNQKLIEAGNINAQAFLAKPYTLQQLLHTIQGVLSVP
>NZ_CP019636.1|WP_087538271.1|1016319_1019895_-|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase
MQQRSFATIDGNEAVAKVAYQLNEVVAIYPITPSTPMGEWADTWAAEGTPNLWGTVPTIIEMQDEGGVAGTIHGALQTGALTTTFTASQGLLLMIPNMYKIAGELTPTVFHVASRSLAAQGLSIFGDHSDVMATRTTGFALLSCASVQEAQDFALIAQAATLESRIPFLHFFDGFRTSHEISKVELLTLQDLQALIDENFILEHRARALSPDHPVLRGTAQNPDVYFQARETVNPYYTACLNIVQSYMDKFAKQTDRHYHLFDYHGAMDAERVIVSMGSSCEVVHETVDYLNARGEKVGVVKVRLYRPFDAIKFVESLPETVKAIAVLDRTKEPGSAGEPLYLDVVTAIHEAADSPVPRAVGGRYGLSSKEFTPAMVKAIFDNLAMAEPKNHFTVGINDDLSYTSLDYDPEFSIEPDHIIRAIFYGLGSDGTVGANKNSIKIIGGETENYAQGYFVYDSKKSGSVTISHLRFGSQPIRSSYLIKKANFIACHQWGLLERFDMLKHIVPGGTFLLNSPYSKQELWQHLPRVVQEQILNKHLKFYVINAYKVARESGMGGHINTVMQVCFFALSGVLSKEEAITQIKLYIRKIYSKKGDEIVEMNLRAVDQTLEYLYEVSVPNSVESNIELRPPVPDTASEFVHEVLGKMIAGYGDEIPVSALPADGTYPTGTAKYEKRNIAQEIPVWDADVCVQCGKCVMVCPHSVIRSKVYDPQNLENAPATFKSTDAREHDWKGLKFTIQVAAEDCTGCGICVDVCPAKNKAQPRLKAINMQPQAPLQEQERENWNFFLSIPNPDRRELKLTHINHQQMQEPLFEFSGACAGCGETPYIKLVSQLFGDRALIANATGCSSIYGGNLPTTPWTQNSEGRGPAWSNSLFEDNAEFGLGFRVSIDKQREFACELLTQLAPEIGESLVESILNAEQKDEADIYEQRQRVSLLKQGIDELIEDSKTRGHGDAEKVRKLKSFKSLADLLVKKSVWIIGGDGWAYDIGFGGLDHVLASGRDVNILVLDTEVYSNTGGQMSKATPRGAVAKFAAAGKPAAKKDLGLIAMSYGNVYVASVAMGARDEHTLKAFLEAEAYSGPSLIIAYSHCIAHGINMSTAMQNQKAAVDSGRWLLYRFHPDRMNQGENPLQLDSRTPKLSVEQYMYLENRFKMLTKSHPEQAKRLLQQAQEDVKHQWQMYQYLVAREF
>NZ_CP019636.1|WP_087538270.1|1015270_1016302_-|dihydroorotate-dehydrogenase-like-protein
MDITTTYMGLKLRSPLVASASPLSENIDNIKQMEDAGAGAVVMHSLFEEQLRLERYELHHHLTHGTESYPEALTYFPEPESFRVGPEEYLDHICKIKRSVKIPIFASLNGSSLGGWTSYARQIQQAGADALELNIYYVPTDIDLTAQQIEQTYIDILKAVKAVVTIPVAVKLSPYFTNMGNMAKQLDEAGANALVLFNRFYQPDINLKTLEVEPNVLLSTDQSMRLPLRWIAILYGRINTSLAATSGIHKGEDVVKMLMAGANITMLCSVLLQHGINRIQIIEQQLRQWMKEHEYESVQLMQGSMSQQYCPNPSEFERAQYMRAIQTYKLEWRQIYEASHYFG
>NZ_CP019636.1|WP_087538269.1|1014089_1015190_-|hydrogenase-formation-protein-HypD
MKFIDEYRDAKVAQKYAEAISAITTKPWKIMEICGGQTHSIVKFGIDKLLPKEITLIHGPGCPVCVTPVEFIDKAIAIASLPEVIFCSFGDMLRVPGSQKDLLTVKADGGDIRIIYSPLDVLKIAQAHPNKQVVFFAVGFETTAPATAMAVYQAYQQGIKNFFLLVSHVLVPPAMTAILASPHNQVQGFLAAGHVCTVMGYTEYEPIARNYHIPIVVTGFEPLDILQGVYLCVKQLEEGRSQIENQYTRSVRRSGNEVAQQLIQEVFEKVPRKWRGIGEIPQSGLTLREKYIEFDAEQRFSLVNCTVRESAECISGLILQGVKKPCECSAFGRNCTPEHPLGAPMVSSEGACAAYYRYRQQTAIEL
>NZ_CP019636.1|WP_087538278.1|1030906_1031326_-|hypothetical-protein
MAVNYRERIITLWSVFLLGMLFHTQLNLIPLFHGLPVVESQKATNIDEIAVIMWLMLGFFVIPMLAMIATAFTDSKRYRMIHFGLTIFYSIMNLLHLLLDLFVQPLLWYQIVLMVFLLLVGLLLNLTAFQWLRLPFKAN
>NZ_CP019636.1|WP_087538279.1|1031397_1031943_-|oxidoreductase
MARLKLATVWLGGCSGCHMSFLDLDEWLIDLAGQVDLVYSPFADIKEYPQGVDIVLVEGAVANEDHLQMIQTVRERSQILVSFGDCAVTGNVTALRNPLGSAEPVLQRCYIEAVDVHGMIPSEPGIVPTLLDRVIPVHTVVPVDVYLPGCPPSATRIKAVLEALLRGEKPQLEGREFIKFG
>NZ_CP019636.1|WP_087538280.1|1032005_1032530_-|DUF3122-domain-containing-protein
MLSRIFKTFLWLLLLGMITVYIFLGLASFTSQQVIAVVVQLEEAPGEILYRSQQKLNDELGNYWQVVLFKRVHSNTNTVSSINLRLIGFPGSQELPHPLPLKIITQTNEVLTAPDIFVEEAPAPTIGQYDFKDILPQLPTQELLIGIPLGAERFINISIPQYVVQEWQEVAFKH
>NZ_CP019636.1|WP_087538281.1|1032566_1033283_-|bidirectional-hydrogenase-complex-protein-HoxU
MAVKTLTINERLISAREEETILQAAQDAGIHIPTLCHLQGVTDVGACRLCLVEIAGSHKLQPACVTKVAEGMEVQTNSDRLQKYRRMIIEMLFAEGNHICSVCVANGNCELQDLAIEMGMDHVRLEYQFPNRKVDASHEHFGIDHNRCVLCTRCVRVCDEIEGAHTWDMAGRGTNSHVITDLNQPWGTSETCTSCGKCVNACPTGAIFYQGSGVGEMKRDRAKLDFLVTAREKKQWLV
>NZ_CP019636.1|WP_087538282.1|1033300_1034905_-|NADH-quinone-oxidoreductase-subunit-L
MDLTELQEIAQKEHGNSKPIRIRCCMAAGCLSSGSTAVKESLEKVTTEIGLADKVEVCSVGCMGLCCQGPLVQVDSKEAQDLEPLLYEKVTSENALSIIAALDDDTVKVQKGDLKHPFFTKQLPIVLENSGEVDPERIESYIAAHGYQALYHLLREMTPAEVVDAMTRSGLRGRGGAGYPTGVKWATVAKAKGERKFVICNADEGDPGAFMDRSVLESDPHRVLEGMAIAAYAVGANQGYIYIRAEYPIAINRLQIAIRQAQRLGLLGSHIFDSPFDFKIDIRIGAGAYVCGEETALMASIEGKRGTPRPRPPYPAESGLWGFPTLINNVETFANVPWIIRKGAEVFASIGTEKSKGTKVFALAGKIRNTGLIEVPMGTTLRQIVEEMGGGVPNGGTSKAVQTGGPSGGCIPASAFDTPVDYESLAQLGSIMGSGGMIVMDESTNMVDVARFFMEFCMDESCGKCIPCRVGTVQLYQLLTKIREGKASLADLELLEELCDMVKQTSLCGLGQSAPNPVFSTLRYFRDEYLALIQ
>NZ_CP019636.1|WP_087538283.1|1034988_1035528_-|bidirectional-hydrogenase-complex-protein-HoxE
MDSQTVNKKNQYAKSTLKEHLSGDKRFKILDATMKRHQYQQDALIEVLHKAQELFGYLENDLLFYIAHSLKLPPSRVYGVATFYHLFSLAPKGVHSCVVCTGTACYVKGAANLLATVEKYAKIHAGETTPDKELSLLTARCLGACGIAPAVVFDGTVCGHQTPELVTEKIEGWLKPVNS
>NZ_CP019636.1|WP_087538284.1|1035844_1038361_-|magnesium-translocating-P-type-ATPase
MNKQRIFWSIPMAELLQQLQSTPQGLTTQAAKQRLEEYGANLLKPKKKSDTLTLLLAQFQSPIILILIAAAILSIFLNDKTDALIILIIVLVSGLLGFWQERGAADAIEKLLLIVQIKANVLRDGKSVDILVEEIVPGDVVCLAAGDNIPGDCIILDSKDLFVNEAALTGETYPVAKVDGVLPLQTPLSQRTNTLFMGTYVVSGTAKALVVGTGKETEFGKVSQRLKFRPPETEFEHGVRQFGYFLMEVTLLLVLGIFAGNLLLKRPVLDSFLFALALAVGLTPQLLPAIISINLAHGAKQMAHKSVIVKRLAAIENFGSMNVLCSDKTGTLTEGVVRIHSAVDYKGNESDRVLFYAYLNAIFETGFVNPIDQAIRSDRTFDISGYQKLDEVPYDFIRKRLSILVAKDHTQLVISKGALQSIINVCSFVETGECTIVELNSLQAQIQQRFEALGQEGFRVLGVAYRNPTTTTLSKEDESDMTFLGYLVFFDPPKPGIIHTITELKQAGVSLKIITGDSHAVAASLSQQIGLSQPKILAGLDLHEMSDEALMHQVNLIDVFAEVEPNQKEDIILALKKAGNVVGYMGDGINDASALHAADVGISVNSAVDVAKEAADIVLLEQDLDVLLQGIGEGRITFANTLKYVFMATSANFGNMFSMAGASLLLPFFPLLPKQILLTNLMTDFPEMTIATDRVDQEMVKQPHRWDIKFIRNFMIVFGMLSSVFDYLTFCILLLILHSTPNQFRTGWFMESVISASMIVLVIRTRQPFFQSKPGKYLLIATITIGIVTLLLPFTPLAKLFGFQPLPISFILALGVIVALYITAAEKVKQKFYRQIKF
>NZ_CP019636.1|WP_087538285.1|1038412_1041025_-|HAD-IC-family-P-type-ATPase
MTHQIEINSISGLSESVAFVRLKQEGYNELPSTLNRSIWKIALESIQEPIFLLLVACGVIYLFLGDAQEALILLGFVFLIVGINLYQEQKTEKSLEALRDLSSPRALVIRDGKRQRIAGREVVGGDIVVLAEGDRVPADAVVLWSTQLSVDESLLTGESVPVRKRAVEDTLELELATQSSRKHRPGGDDFPFVYSGTLIVQGQGIAQVYATGMQTEMGKIGKALQTVEPEDTVLQRETRRIVSKLTIVAIAICIAVIIIYGITRSDWLQGFLAGLALAMAILPNEIPVVLAIFLALGAWRFSLTRVLTRRIPVVETLGSATVLCVDKTGTLTFNRMSIQQLFVYEPSYQSPHFYDVTLHEREPLPEAFHELIEFGILASRKDPFDPMEKALKQVGDVHLAKTEHLHYDWEILREYPLSGQLLAMSCVWQSPEGKLLIATKGAPEAIADLCHFDAKQMQNLEQHISTMAAAGLRVLGVAKAVGRHKSDKKQNLLPDKQHDFEFQFLGLVGMADPVRPTVASAIAECYGAGIRVVMITGDYPATAQNIARQIGLHPSTQVITGTELEQMTEGELSAQIQTVNIFARVVPEQKLLIVNALKQCGEIVAMTGDGVNDAPALKAAHIGIAMGKRGTDVARESADLVLLDDDFSSIVQSVRLGRRVFDNLKKGMAYTLAVHVPIAGMSLIPVMFHWPLVLLPIHIAFLHLIIDPACTVVFEAEPEESNIMNRPPRNPKEPLFSRRTLRLALLQGISVLVVLLVVFAIAFYSGHGELDARALAFTTLIVSNLSMILTNRSWSRTIPEMLRAPNAALWWVLGGAVVFLGLVLYVPLLRHLFRFSFLHFDDLVVSLTSGLFSILWFEGLKIWQRRRGFV
>NZ_CP019636.1|WP_087538286.1|1041131_1043924_-|bifunctional-acetate--CoA-ligase-family-protein/GNAT-family-N-acetyltransferase
MQKSMQLGSDRAYDILRSEHQPLDAIFAPKSIAVIGASDREGSVGRTVLWNLISHPFGGTVFPVNPKRYNVLGIKAYPNIAAVPEPVDLAIVITPAPTVPYVIGECVDAGVKGAIVISAGFKEIGTAGAELERQVLQQVCRGKMRLIGPNCLGVMNPHTYLNATFANGMALPGKVGFISQSGALCTAILDWSFHENVGFSAFISIGSMLDVGWGDLIYYLGDDPHTESIVIYMESIGDARSFLSAAREVALTKPIIVIKAGRTEAAAKAAASHTGALVGSDTVFDTALRRCGVLRVKSISDLFDMAEVLAKQPRPKGPKLTVITNAGGPGVLATDALITDGGELAELSPQTYEALNQLLPPQWSHNNPIDILGDADPSRYAKALEIAANDPSSDGLLAILTPQAMTDPIQTAYQLKPFAQIGKPVLASWMGDVDVEAGAEILNQASIPTFAFPDTAAHVFNYMWRYHYNLRALYETPVVPEQADTPDRTVAKTILQNARQAGRTLLTEVESKQILAAYGIPTVVTQVATSAEEAVQLAEEIGYPVVLKVFSQTITHKTDVNGVHLNLHDAKAVREAYDAIALSVSTKVGASEFAGVTVQPMIDLKNSYELILGSSIDSQFGPVLLFGTGGQLVEVFQDQALGLPPLNTTLARRMMEQTRIYKALQGIRGIKAVNLEALEQVLVRFSQLVVEQRFIKEIDINPLLVKAEEHQESKPELTQNSLVALDARIILHDLDIAEAQLPKLAIRPYPTQYVSPWTMRNGTQVTIRPIRPEDEPLMIKLHKTLSEESVFFRYFHLIKLSQRIAHERLTRLCFIDYDREMALVVDYQNPETEEHEILAVSRLSKLHGTNEAEFAILVSDRYQCQGVGTELLKRLLQVGRDEQLTLISAEILTENSAMQRVCEKLGFCIHPTADASVVRAEIKLGCQHLE
>NZ_CP019636.1|WP_087538287.1|1044068_1046516_-|phosphoenolpyruvate-synthase
MLETFVTQKTPSQNVKQQALVLPLDVVGIADIPLVGGKNASLGEMIQQLKSKGVRVPTGFATTAYAYRFFIQAAGLETKLREIFASLDVENVNNLRQCGKQARALMLQTPFPQELEKAIAQAYQDLCEQYGTDTDVAVRSSATAEDLPDASFAGQQETYLNVHGLQAVLQACHKCFTSIFTDRAISYRQIKGFDHFNIALSVGVQKMVRSDLATSGVMFSIDTETGFKDAALITAAYGLGENVVQGAVNPDEYLVFKPTLKQGYRPILEKRPGTKEIKMVYDLGGSKMTKNIPVAASDRAAFALKDEEILQLAHWACFIEEHYSQVRGVYTPMDIEWAKDGIINELFIVQARPETVQSQKIKNVLHTYQLKEKGEVLVTGRSVGEMIGQGKARVILDVHCLSEFQPGEVLITNRTDPDWEPIMKKASAIVTNSGGRTCHAAIIAREMGIPAIVGCNYATTLIKTGQEITVSCAEGETGKVYKGLLPYEVQEIPLEKLPRTRTKIMMNVGNPEEAFGYSAIPNDGVGLARMEFIIANYIKTHPLALVHFDELEDELAKYKIAELTAGYEDKGQFFVDKLAQGIGTIAAAFYPKPVIVRLSDFKSNEYANLLGGKQFEPQEENPMLGWRGASRYYDERYQEGFALECRAMKKVRDEMGLTNVILMVPFCRTPSEGRRVLAEMAKHGLVRGENGLQVYVMCELPSNVQLADEFCEVFDGFSIGSNDLTQLTLGLDRDSELVAHLFDERNEAVKQMIAKAIQTVKKRDHKIGICGQAPSDYPEFARFLVEEGIDSMSLNPDSVLKTLLEVAATENRFEV

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Crispr_ID: NZ_CP019636_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_3

1455279-1455367

Orphan

Consensus_repeat	Method
CTGTTACTTTCCACGGTTAGGCGCTGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_3

>merge|NZ_CP019636|3|1455279-1455367|CRISPRCasFinder
CTGTTACTTTCCACGGTTAGGCGCTGGTTTCCGCTTTTGCTACTTAAGAATCAAAATTAGCACTGTTACTTTCCACGGTTAGGTGCTGG

>NZ_CP019636|3|3|1455279-1455367|CRISPRCasFinder
CTGTTACTTTCCACGGTTAGGCGCTGG	TTTCCGCTTTTGCTACTTAAGAATCAAAATTAGCA
CTGTTACTTTCCACGGTTAGGTGCTGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087538582.1\|1456617_1456821_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_157679287.1\|1449009_1450065_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340831
NZ_CP019636.1\|WP_087546056.1\|1456972_1457863_+\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851
NZ_CP019636.1\|WP_087538588.1\|1465542_1466352_+\|WecB/TagA/CpsF-family-glycosyltransferase	unknown	unknown	gnl\|CDD\|377136
NZ_CP019636.1\|WP_087538586.1\|1462909_1464736_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|153073
NZ_CP019636.1\|WP_087538590.1\|1467055_1469167_-\|TIGR00300-family-protein	unknown	unknown	gnl\|CDD\|224827
NZ_CP019636.1\|WP_087538584.1\|1458891_1460529_-\|CTP-synthase	unknown	unknown	gnl\|CDD\|235437
NZ_CP019636.1\|WP_087538585.1\|1460707_1462498_+\|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl\|CDD\|223929
NZ_CP019636.1\|WP_087538580.1\|1455042_1455237_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538577.1\|1450080_1452300_-\|O-linked-N-acetylglucosamine-transferase,-SPINDLY-family-protein	unknown	unknown	gnl\|CDD\|226428
NZ_CP019636.1\|WP_087538583.1\|1458080_1458515_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538589.1\|1466415_1466943_-\|DUF2085-domain-containing-protein	unknown	unknown	gnl\|CDD\|378277
NZ_CP019636.1\|WP_087538579.1\|1453619_1454993_+\|thioredoxin-disulfide-reductase	unknown	unknown	gnl\|CDD\|273540
NZ_CP019636.1\|WP_087538574.1\|1447219_1447441_-\|DUF4327-family-protein	unknown	unknown	gnl\|CDD\|372966
NZ_CP019636.1\|WP_087538578.1\|1452512_1453064_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|374761
NZ_CP019636.1\|WP_087538581.1\|1455566_1456457_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224094
NZ_CP019636.1\|WP_087538573.1\|1445907_1447122_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP019636.1\|WP_157679285.1\|1445364_1445568_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538575.1\|1448454_1448853_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379646
NZ_CP019636.1\|WP_087538572.1\|1443092_1445129_+\|serine/threonine-phosphatase	unknown	unknown	gnl\|CDD\|237756

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_157679287.1\|1449009_1450065_-\|glycosyltransferase	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct 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. The members of this family are found mainly in certain bacteria and archaea.	1.92156e-41
NZ_CP019636.1\|WP_087538573.1\|1445907_1447122_+\|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.	3.92757e-77
NZ_CP019636.1\|WP_087538588.1\|1465542_1466352_+\|WecB/TagA/CpsF-family-glycosyltransferase	gnl\|CDD\|377136	pfam03808, Glyco_tran_WecB, Glycosyl transferase WecB/TagA/CpsF family.	4.95199e-68
NZ_CP019636.1\|WP_087538590.1\|1467055_1469167_-\|TIGR00300-family-protein	gnl\|CDD\|224827	COG1915, COG1915, Uncharacterized conserved protein [Function unknown].	0
NZ_CP019636.1\|WP_087538585.1\|1460707_1462498_+\|N-acetylmuramoyl-L-alanine-amidase	gnl\|CDD\|223929	COG0860, AmiC, N-acetylmuramoyl-L-alanine amidase [Cell envelope biogenesis, outer membrane].	4.33728e-65
NZ_CP019636.1\|WP_087538586.1\|1462909_1464736_+\|hypothetical-protein	gnl\|CDD\|153073	cd03603, CLECT_VCBS, A bacterial subgroup of the C-type lectin-like (CTLD) domain; a subgroup of bacterial protein domains homologous to the carbohydrate-recognition domains (CRDs) of the C-type lectins. CLECT_VCBS: A bacterial subgroup of the C-type lectin-like (CTLD) domain; a subgroup of bacterial protein domains homologous to the carbohydrate-recognition domains (CRDs) of the C-type lectins. Many CTLDs are calcium-dependent carbohydrate binding modules; other CTLDs bind protein ligands, lipids, and inorganic surfaces including CaCO3 and ice. Bacterial CTLDs within this group are functionally uncharacterized. Animal C-type lectins are involved in such functions as extracellular matrix organization, endocytosis, complement activation, pathogen recognition, and cell-cell interactions. CTLDs may bind a variety of carbohydrate ligands including mannose, N-acetylglucosamine, galactose, N-acetylgalactosamine, and fucose. CTLDs associate with each other through several different surfaces to form dimers, trimers, or tetramers from which ligand-binding sites project in different orientations. In some CTLDs a loop extends to the adjoining domain to form a loop-swapped dimer.	1.92334e-18
NZ_CP019636.1\|WP_087538577.1\|1450080_1452300_-\|O-linked-N-acetylglucosamine-transferase,-SPINDLY-family-protein	gnl\|CDD\|226428	COG3914, Spy, Predicted O-linked N-acetylglucosamine transferase, SPINDLY family [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP019636.1\|WP_087538589.1\|1466415_1466943_-\|DUF2085-domain-containing-protein	gnl\|CDD\|378277	pfam09858, DUF2085, Predicted membrane protein (DUF2085). This domain, found in various hypothetical prokaryotic proteins, has no known function.	3.22366e-05
NZ_CP019636.1\|WP_087538579.1\|1453619_1454993_+\|thioredoxin-disulfide-reductase	gnl\|CDD\|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	1.8219e-152
NZ_CP019636.1\|WP_087538574.1\|1447219_1447441_-\|DUF4327-family-protein	gnl\|CDD\|372966	pfam14217, DUF4327, Domain of unknown function (DUF4327). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 80 amino acids in length.	1.70541e-32
NZ_CP019636.1\|WP_087538578.1\|1452512_1453064_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|374761	pfam16734, Pilin_GH, Type IV pilin-like G and H, putative. Pilin_GH is a family from Cyanobacteria. All the proteins are putatively annotated as being general secretion pathway proteins G and H, and are likely to be pilins of the type IV secretory pathway.	1.1519e-29
NZ_CP019636.1\|WP_087538581.1\|1455566_1456457_+\|ABC-transporter-permease	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.18113e-78
NZ_CP019636.1\|WP_087546056.1\|1456972_1457863_+\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	2.24813e-78
NZ_CP019636.1\|WP_087538584.1\|1458891_1460529_-\|CTP-synthase	gnl\|CDD\|235437	PRK05380, pyrG, CTP synthetase; Validated.	0
NZ_CP019636.1\|WP_087538575.1\|1448454_1448853_+\|hypothetical-protein	gnl\|CDD\|379646	pfam14559, TPR_19, Tetratricopeptide repeat.	0.000760007
NZ_CP019636.1\|WP_087538572.1\|1443092_1445129_+\|serine/threonine-phosphatase	gnl\|CDD\|237756	PRK14559, PRK14559, serine/threonine phosphatase.	0

>NZ_CP019636.1|WP_087538580.1|1455042_1455237_-|hypothetical-protein
MAYQQRLKPWAVVHLISSSQKVVVSRHRSRTDAEGYVQLLRQQMPGSQLDVLFEPAEDKSFQST
>NZ_CP019636.1|WP_087538579.1|1453619_1454993_+|thioredoxin-disulfide-reductase
MTNPTVENVVIIGSGPAGYTAAIYAGRANLKPVVFEGFQAGGLPGGQLMTTTEVENFPGFPEGITGPELMDRMKAQAERWGAELYTEDVIEVDLSQRPFTVRSEEREFKTHSIIIATGATAKRLGLDSEHQFWSRGISACAICDGATPIFHGAELAVVGGGDSAAEEAIYLTKYGSKVNLLVRSDKMRASKAMQDRVLSNPKITVHWNTQPIDVFGNEKHMEGIRIHNTDTGEEKDLHVKGLFYAIGHTPNTSLFKEHLELDDVGYIVTKPGSPETNIEGVFAAGDVQDHEYRQAITAAGSGCSAAMLAERWLSASGLIQEFHQKPETPDNEIEQPAETKTEEQKAAEFDLNSTRHYGGYALRKLFHDSDRLLVVKYVAPGCGPCHTLKPILNKVVDEFDGKIHFVEIDIDKDRDIAENAGVTGTPTVQFFKDKDLLKELKGVKQKSEYRQLIESNL
>NZ_CP019636.1|WP_087538578.1|1452512_1453064_-|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MKTELKAKFLQHILQKKKQDEGFTLIELLVVIIIIGILSAIALPSFLNQANKARQSEAKTYVGSMNRAQQAYYLENNSFAKNADFGKLGLGVATQTENYKYNIADGTSGVNNQAQPIKDKAPVKAYVGGVMIGTVSATSEATTLAILCEAEKAVTNGGDDGTALYKLNGTAPTCPDNYVSAAK
>NZ_CP019636.1|WP_087538577.1|1450080_1452300_-|O-linked-N-acetylglucosamine-transferase,-SPINDLY-family-protein
MITDFMNWQQQAHQYLVKGEYSQAAKLYEQAITAEPDILSHYWHLGLLLLLQGQEAEAQMTWMLPMTEAEEDQIQIFTNELIQVLQAEAQRRETLAEYSLAWIIRQHIREINTTDINNLLKIIQLSIKLEKFEDIELQQVRLIELLQVRQSKDFNAEFLLQVLQQVLETAPLHPAILELVEACLPYFSKPDDCFCLLLPIAMKIGHTFKQPALAASFLELCLCLDAQNIETLRHLAIFYQDAGRYSQGIETAKLCYSLSQTLPDKIFATHLVLRALMTAGGYWNEVCSTCQELESLLKSFIKAQPLPLDELRTLRLLTPSFAIPHIKDCPAEFREIHNQIAQIFQTNIQAITQKESKIYSQHHSNQKYSVIFSTRKLKIGYLSYAFRQHSVGWLARWLFQHHNRDNFETHAYFVNYKLIDDWLQDWYVNQASQAHTLGMNGLEIAEKIYQDEIDILVDLDSITLDISCEVMALKPAPIQVTWLGWDASGIPAIDYFIADPYVLPGSAQDYYTEKIWRLPQTYIAVDGFEVGVPTLRRDELNIPADAVVYLSAQRGYKRHPETTRWQMKILKEVANSYFLIKGSSEEEAIKRFFYKIAEEEGVNCSRLRFLPQVALESVHRANLGIADVVLDTYPYNGATTTLETLWMCIPMVTRVGEQFVARNSYTMMMNAGITEGIAWTDEEYIEWGIRLGKDEALRQQIAGKLRQSKATAPLWNGKQFTREMEKAYEQMWANYLEKS
>NZ_CP019636.1|WP_157679287.1|1449009_1450065_-|glycosyltransferase
MDKLRILIITNLYPPQAIGGYERGMADCARLLAHRGHTVLVLTSNTEKYGTNYTTTDTEPSVNRCLYLCGAWTKEGTHWFSAEQVLTRTFYNRQTVALEVQTFKPDVCLVGNIDFLGLELIEKILANEIPVAHYVMNANPGYVAELAPNSKLHQYITCSNWIREGLNQQGYPVETAQTIYPGAAVDEFYQAELPPRDRLRIAYASLVMHYKGADVLIEALSLLHAAGVEFSATIAGGTLQPQFVQALQEFVESEGMQDKVKFPGVLSRQQLKELYRSHNVLVFPSRFQEPFGISQIEAMAAGLTLVTSGTGGAGEIVENGKDGLIFESENPLDLANVLCFLYQFIQMSGKE
>NZ_CP019636.1|WP_087538575.1|1448454_1448853_+|hypothetical-protein
MASSGEQYRIARHQKIERRKRILTIVSIVSFLSSGVFAIVPTLQQAIQNPQSAPASTELSLHQQAQGFELVLQREPENQVALYGLVNVRLRLQDVQGAIAPLEKLVKLQPEHRHYKTLLEQLKKQGDKSDRS
>NZ_CP019636.1|WP_087538574.1|1447219_1447441_-|DUF4327-family-protein
MSKQQVIHPMVKLQRNVRSLVDSNIIKPTDSIWKIALLFGNEWQYWKQELLDFGFSMQDPVSELLAVEAWDEE
>NZ_CP019636.1|WP_087538573.1|1445907_1447122_+|protein-kinase
MVTLTLLEPQKKTPIKQWHFDDETVIRIGRSADNDIVLSDSLVSRHHLELRQIGSDHNGSSWQVISQGTNGTFLNGVLVTQSWLPDDSLLQLAQGGPILKFQIDQQTLSQNSPSTSHTCTHEGNLPNNLFCIHCGQPLSVIQTIRHYQVLRILGQGGMGTTYLAWDGQGKIAGHPQLLVLKQMNADMAKIAKAQELFEREANTLKSLNHIGIPKYYNFFVEGGKKYLAMELVHGQDLEKLIYSKGPVTPNLAINWMIQTCDILDYLHSQEPPLIHRDIKPANLMVRNSNNRIVVLDFGAVKEIGTTPGTRIGAEGYCAPEQERGQPLTQSDLYAIGPTLIFLVTGESPFKFYRQRGRNFRFEVGNVPTITPQLREVIDRATEPLPRDRYQTAKELAAALAECKV
>NZ_CP019636.1|WP_157679285.1|1445364_1445568_+|hypothetical-protein
MPTRSISLEQGLMELDLPVAVRASQLFWSLRSPPSNNALLVCLLRVPGYLANANVSSQGVENSSGIS
>NZ_CP019636.1|WP_087538572.1|1443092_1445129_+|serine/threonine-phosphatase
MLICPQCKFENPNTNKFCQNCGASLTQKVCSECGTHMALNAQQCDNCGAECGTVLWAIITKEATFAAGENKEDEQVGEVGEVTEVEEVGEDKFICLSPSTSSSPSPLPVGSYLDPQQRYQLLEPLPALGEIAPNTEVCIKVLDCQPYQVSLLEVMLANQQQGLATLSMDTNKIPSLAKLYIDLQSWSHLGIPPIHDAWQQDNIQVVLIEDRSNWQELLYLWREDTTSSLQIVHFLYQMTQLWSVLETVNCRQSLLELSNLRLDEDESLALQRLYVESPDNQYNVELPEDIETTAPDTTEAQVFTVQVLGRVWQALFRQSQRTQFGSILHLIGDLELGKIQTLGQLQSRLEAIASEFQGNPTSIPSVTSKMSQTPATATILQLDDEEQYETDSKGDDVPTIVLPMQLVSLENAGLTDVGRQRDHNEDYFGIETKIQKLELPNKRTLQVRGLYVLCDGMGGHAGGEVASALAVNSLRQYFQTNWALNKLPSEDDIRKAVRQTNQAIFDLNQKDARSGVGRMGTTLVMVLIQDNQVAVANVGDSRLYRVTRKRGLEQITVDHEVGQREISRGVEPSVAYSRPDAYQLTQALGPRDEHSIIPDVQFFEINEDTLFVLASDGLSDNDLLTIHWQTHLAPLLSSSANLESGVRALIDLANHYNGHDNITAIIIRAKVRPNLEQQ
>NZ_CP019636.1|WP_087538581.1|1455566_1456457_+|ABC-transporter-permease
MTIIKSPQLRFLRFTKRPSLSQQLMLIGLMMTLFFLFLALCAPLFQAFGWVQNPTDSLSNPIQEPPSLQHWFGTSREGYDVFSRTLFGAQAALQVVLLATTLSMLIGVPLGMLSGYVGGRLDKALLFLMDSIYTLPGLLLSVTLAFIVGRGILNAALAISIAYVPQYYRVVRNHTVSVKTEVFIEAAQAMGANTWQVLSRYLFFNVIQSVPVLFTLNAADAILILGGLGFLGLGLPRETPEWGRDLQQALQALPVGVWWTALFPGLAMTTMVVGLSLLGEGLNEFINPRLRKDIRK
>NZ_CP019636.1|WP_087538582.1|1456617_1456821_+|hypothetical-protein
MKDNFSLIAAAAGGFMLSVALTGILRGAPVASLEGQPSFRTLTVATLRPAPKESENVKFFGSETDNQ
>NZ_CP019636.1|WP_087546056.1|1456972_1457863_+|ROK-family-protein
MNSQVIGIDLGGTAIKLGRYATDGTCLQSLSVATPQPSTPEAVVAAMVDAIAQIDPESQTIAIGVGTPGPADAEGRIAKVAINLTGWHDVPLAEWLEAKTDKPTIVANDANCAGLGEAWLGAGRRFQNFILLTLGTGVGGAIIIDGRLFTGHFGAAGELGLITLNPDGPKCNSGNQGSLEQYLSVPAIRRRTGKEPAELGALAKSGDAKALTFWQEYGSDLGIGLTSLIYVLTPEAVVIGGGVSASSEFFISSAKAEIERRVMPTSRYCLQILPAELGNFAGISGAAKLAFSKLAG
>NZ_CP019636.1|WP_087538583.1|1458080_1458515_-|hypothetical-protein
MAYWVKIHYERNEYVVNFEHVTAFCHERNGRVTFWLPDCAMPIVVNPQNNLEDYQKILEYIEHITGLGFEYSYWVKINYERNEYIVNLDSISSFRYEPNNGRITFWIPDGNVPIIINPVSNPESYQKVLEYIQNTTGCILEVNN
>NZ_CP019636.1|WP_087538584.1|1458891_1460529_-|CTP-synthase
MTKFVFVTGGVVSSIGKGIVAASLGRLLKSRNYSVSILKLDPYINVDPGTMSPFQHGEVFVTQDGAETDLDLGHYERFTDTSMSRLNSVTTGSIYQAVINKERRGDYNGGTVQVIPHITNEIKERIIRVAKDTNPDVVITEIGGTVGDIESLPFLEAIRQFRKDVGRQNVLYMHVTLVPWIASAGEMKTKPTQHSVKELRSIGIQPDILICRCDRPLAAGLKQKLSEFCDVPAECVIPAQDAKSIYEVPLILEREGLAQQTLELLNMEQRQPDLGQWQTLVEKLYSPKNRVEIAIVGKYVRLSDAYLSVVEALRHAAIAMSSELHLRWVNSEKLEVEGVETYLEGVDGIIVPGGFGVRGVDGKIAAIKYARNCQIPFLGLCLGMQCSVIEWARDIAGLTDANSAEFDPHTNNPVINLLPEQQDVCDLGGTMRLGLYPCRLLVNSLAFKLYQEEVIYERHRHRYEFNNAYRNLFIDSGYVISGTSPDGRLVEIIEFPNHPFFISCQFHPEFQSSPSTPHPLFKGFIQAAIARSHPSSRTQTPAQVS
>NZ_CP019636.1|WP_087538585.1|1460707_1462498_+|N-acetylmuramoyl-L-alanine-amidase
MRPLFELVLLGFIVTPSVALAQEQSLKIVYPKTNYQTTAKKIFFIGTAPSSGQVFINGKPISRSKSGHFAPSLPLQLGENLFTVRYQNQEVQIKVTRASTQPEVPQGLAFVKNSLTPAVDIAKLPGELICFSAIAAPNATVSVKLANQSVSLLPQPQQAQLPANSAALTGQNQPSAQFSAVKYQGCTTVQTSGNLGQPQFELTRDGKTITQAGSGKVQILSPTQLEVVEVTADSGVARTGPTTDYSRLTPLPKGTRSAVTGREGEWLRLDYGAWINSKETRTLPGAIPPQSIIRSVGYRQLPGVTEMVFPLQVPVPVSVQQGNQTFTLTLYNTTAQTDIIRLDDDPLISRLDWQQLPTLGSRQGGVQYTFNLKKAQQWGYKLRYEGTSLVLGLRHSPLISSRSRGVFRKQKPLSGLKILLDPGHGGKESGASGPTGYLEKDVNLAVSKLVRDELVKRGATVVMTRENDTDVSLVDRVAKIDKEEPAIAISIHYNSLPDEGDAENTSGMGSFWYHPQAHSLAVFMHNYIVSQLKRPSYGVFWDNLALTRPASAPSVLLELGFMSNPNEFEWVTNSREQKKLARVIANGIVEWFRSDR
>NZ_CP019636.1|WP_087538586.1|1462909_1464736_+|hypothetical-protein
MVQTLNVSGTTNYASGASPKVLAPNLSITDPNNGNLNGASVVITSNFNATQDRLGIAGQTGTSGTIQGLNWNYDTTTGVLTLTGTAANDVYQNVLRQVTYSNTNGTPSGGARGIEFALGTNLANPENKHFYDFVPLEGGLSWTNAQALAANSTYFGLQGYLATITSATEQNFIQGKVQGNGWIGGSDAGAEGTWRWVTGPEAGTQFWTGGATGSPFENRYSNWASTEPNNLNNVENYAHVIGNPVLDPSVQGRWNDLADVVGPGPYQPLGYIVEYGGLQGDPAVQLTGNVTLTLNSSKFDFSGDSKPDILWRNYTTDETAIWQLGGTTGTTLERSILLPKPADVRWEIEGQADFTNDGNTDILWRNYRTGENAIWQMNDTNFEKATLLTKVEDTAWKIEGQSDFTGDGNTDILWRNYRTGENGIWRMNGTNLEQATLLTKVDDTAWEIQGLADFTGDGKDEILWRNNRTGENGIWQLNGTTLQQSTLLTPVGDLNWEIEGQADFTGDGKTDILWRNYSTGENAVWEMDGITLKEAKLITKVDDVRWEIEGVGDFTGDGKADILWRNYGSDETAVWRMNGINLDESISLSKTGDTAWEISFPSYFPILT
>NZ_CP019636.1|WP_087538588.1|1465542_1466352_+|WecB/TagA/CpsF-family-glycosyltransferase
MKQVNLLNVTINNITMIELLEKLKSGGIVFTPNVDHVMKLQRSQEFYCAYQQADYMVCDSKVLMYISSFLGTPIQEKISGSDLFPAFYTHYKDDEDIKIFLLGAEKSVAKTAQKEINSKVGREIIIAAHSPSFGFEKDEEECQNIVSMINSSDATVLAIGVGAPKQEIWIAKYRKQFKNIKIFLAIGATINFEAGSLKRAPKWMSEVGLEWFYRLLNEPRRLWKRYLLDAIPFFWLILKQRFQLYKNPWKTMMEKDAKQIQPLQLSQKS
>NZ_CP019636.1|WP_087538589.1|1466415_1466943_-|DUF2085-domain-containing-protein
MEGVVFKRQLQIRWVSFVADFLLAGMVVGPLAAPFLAASGLPLLPLIAKIIYFMGSHVCPQPDMGVALAQPHIMAVCMRCYGTVAGLLITRLLYEVTSGKGFYWLSQYDWSGAAFASVLMMAYPLELAAQVLGWWSFNNYIVTLFGLVTGLAWGLFTMPILHGRQQPEATLIQDN
>NZ_CP019636.1|WP_087538590.1|1467055_1469167_-|TIGR00300-family-protein
MTSQIRFLMCAPNHYDVDYVINPWMEGNIHKSSQERAVEQWEQLHHILKEHAIVDLVPPQKGWPDMVFTANAGLILGNTVVLSRFLHKERQGEEPYFKQWFEENGYTVYELPKDLPFEGAGDALLDREGRWLWAGYGFRTELDSHPYLAKWLDIEVLSLRLIDERFYHLDTCFCPLANGYLLYYPPAFDSYSNRLIEMRVQKEKRIAIAEADAVNFACNAVNVDHIVVMNKASEALKARLADTGFQVIETPLTEFLKAGGAAKCLTLRVTEPVREELHANVSVESRIIRIEGHLLDSGLINRALDLITDNGGSFQVLNFLLGEQRQSTSAAEVKVSAPSHDVMESIISHLIDLGAVDLPQDERDAKLEPVTQAGVAPDDFYVSTIYPTEVRIKGEWVKVQNQRMDGAIAITQSPKGLTAQCKILRDLEVGESVVVDVQGIRTIRKTESREQRNAQEFSFMSAGVSSERRVELVVEQVAWELRKIRDAGGKVAVTAGPVVIHTGGGEHLAQLIREGYVQALLGGNAIAVHDIEQAMMGTSLGVDMKRGVAVRGGHRHHLKVINTIRRYGSIAKAVEARVINSGVMYECVRNGIPFCLAGSIRDDGPLPDTEMDLIKAQTEYARLLKSADMILMLSSMLHSIGVGNMTPAGVKMVCVDINPAVVTKLSDRGSVESVGVVTDVGLFLSLLVQQLQKLTSPYTAKVS

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Crispr_ID: NZ_CP019636_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_4

2050782-2050896

Orphan

Consensus_repeat	Method
CCTAGCAGCGAGTTGCTACTCAGGGGAGTCAGTTAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_4

>merge|NZ_CP019636|4|2050782-2050896|CRISPRCasFinder
CCTAGCAGCGAGTTGCTACTCAGGGGAGTCAGTTATTATACAAACATATTGAGGTAATCACCATGACTTCTGACTTATACCTAGCAGCGAGTTGCTACTCAGGGGAGTCAGTTAT

>NZ_CP019636|4|4|2050782-2050896|CRISPRCasFinder
CCTAGCAGCGAGTTGCTACTCAGGGGAGTCAGTTAT	TATACAAACATATTGAGGTAATCACCATGACTTCTGACTTATA
CCTAGCAGCGAGTTGCTACTCAGGGGAGTCAGTTAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087538988.1\|2059789_2060521_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369367
NZ_CP019636.1\|WP_087538981.1\|2046907_2048764_+\|peptidase-S8	unknown	unknown	gnl\|CDD\|173810
NZ_CP019636.1\|WP_087538991.1\|2064397_2065336_-\|ParA-family-protein	unknown	unknown	gnl\|CDD\|224113
NZ_CP019636.1\|WP_087538977.1\|2041950_2043492_+\|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP019636.1\|WP_087538979.1\|2045378_2046200_-\|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	unknown	unknown	gnl\|CDD\|180561
NZ_CP019636.1\|WP_087538980.1\|2046346_2046787_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538992.1\|2065719_2066067_-\|DUF86-domain-containing-protein	unknown	unknown	gnl\|CDD\|225236
NZ_CP019636.1\|WP_017749852.1\|2043822_2044161_-\|P-II-family-nitrogen-regulator	unknown	unknown	gnl\|CDD\|366157
NZ_CP019636.1\|WP_087538975.1\|2040096_2040588_-\|BON-domain-containing-protein	unknown	unknown	gnl\|CDD\|335963
NZ_CP019636.1\|WP_087538983.1\|2049086_2049413_-\|thioredoxin-family-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538976.1\|2040902_2041574_-\|DUF1269-domain-containing-protein	unknown	unknown	gnl\|CDD\|378584
NZ_CP019636.1\|WP_087538982.1\|2048866_2049100_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538987.1\|2057990_2059418_-\|NADP-dependent-phosphogluconate-dehydrogenase	unknown	unknown	gnl\|CDD\|236453
NZ_CP019636.1\|WP_087538986.1\|2056357_2057869_+\|aldehyde-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|143410
NZ_CP019636.1\|WP_087538978.1\|2044450_2045101_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275056
NZ_CP019636.1\|WP_087538985.1\|2054801_2055989_+\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP019636.1\|WP_087538989.1\|2060590_2060869_-\|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	unknown	unknown	gnl\|CDD\|368240
NZ_CP019636.1\|WP_087546097.1\|2060865_2061132_-\|ribbon-helix-helix-protein,-CopG-family	unknown	unknown	gnl\|CDD\|226420
NZ_CP019636.1\|WP_087538984.1\|2052095_2054693_+\|CHAT-domain-containing-protein	unknown	unknown	gnl\|CDD\|378942
NZ_CP019636.1\|WP_087538990.1\|2061465_2064339_+\|isoleucine--tRNA-ligase	unknown	unknown	gnl\|CDD\|215452

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087538988.1\|2059789_2060521_+\|hypothetical-protein	gnl\|CDD\|369367	pfam07444, Ycf66_N, Ycf66 protein N-terminus. This family represents the N-terminus (approximately 80 residues) of Ycf66, a protein that seems to be restricted to eukaryotes that contain chloroplasts and to cyanobacteria.	5.11256e-44
NZ_CP019636.1\|WP_017749852.1\|2043822_2044161_-\|P-II-family-nitrogen-regulator	gnl\|CDD\|366157	pfam00543, P-II, Nitrogen regulatory protein P-II. P-II modulates the activity of glutamine synthetase.	5.03461e-53
NZ_CP019636.1\|WP_087538991.1\|2064397_2065336_-\|ParA-family-protein	gnl\|CDD\|224113	COG1192, Soj, ATPases involved in chromosome partitioning [Cell division and chromosome partitioning].	1.51814e-54
NZ_CP019636.1\|WP_087538977.1\|2041950_2043492_+\|HAMP-domain-containing-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.50417e-16
NZ_CP019636.1\|WP_087538979.1\|2045378_2046200_-\|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase	gnl\|CDD\|180561	PRK06427, PRK06427, bifunctional hydroxy-methylpyrimidine kinase/ hydroxy-phosphomethylpyrimidine kinase; Reviewed.	1.47932e-140
NZ_CP019636.1\|WP_087538992.1\|2065719_2066067_-\|DUF86-domain-containing-protein	gnl\|CDD\|225236	COG2361, COG2361, Uncharacterized conserved protein [Function unknown].	1.48658e-34
NZ_CP019636.1\|WP_087538978.1\|2044450_2045101_-\|hypothetical-protein	gnl\|CDD\|275056	TIGR04211, hypothetical_protein, SH3 domain protein. Members of this protein family have a signal peptide, a strongly conserved SH3 domain, a variable region, and then a C-terminal hydrophobic transmembrane alpha helix region.	0.00189921
NZ_CP019636.1\|WP_087538976.1\|2040902_2041574_-\|DUF1269-domain-containing-protein	gnl\|CDD\|378584	pfam11181, YflT, Heat induced stress protein YflT. YflT is a heat induced protein.	1.2902e-05
NZ_CP019636.1\|WP_087538981.1\|2046907_2048764_+\|peptidase-S8	gnl\|CDD\|173810	cd07484, Peptidases_S8_Thermitase_like, Peptidase S8 family domain in Thermitase-like proteins. Thermitase is a non-specific, trypsin-related serine protease with a very high specific activity. It contains a subtilisin like domain. The tertiary structure of thermitase is similar to that of subtilisin BPN'. It contains a Asp/His/Ser catalytic triad. Members of the peptidases S8 (subtilisin and kexin) and S53 (sedolisin) clan include endopeptidases and exopeptidases. The S8 family has an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure and are not homologous to trypsin. Serine acts as a nucleophile, aspartate as an electrophile, and histidine as a base. The S53 family contains a catalytic triad Glu/Asp/Ser with an additional acidic residue Asp in the oxyanion hole, similar to that of subtilisin. The serine residue here is the nucleophilic equivalent of the serine residue in the S8 family, while glutamic acid has the same role here as the histidine base. However, the aspartic acid residue that acts as an electrophile is quite different. In S53 the it follows glutamic acid, while in S8 it precedes histidine. The stability of these enzymes may be enhanced by calcium, some members have been shown to bind up to 4 ions via binding sites with different affinity. There is a great diversity in the characteristics of their members: some contain disulfide bonds, some are intracellular while others are extracellular, some function at extreme temperatures, and others at high or low pH values.	1.3998e-139
NZ_CP019636.1\|WP_087538987.1\|2057990_2059418_-\|NADP-dependent-phosphogluconate-dehydrogenase	gnl\|CDD\|236453	PRK09287, PRK09287, NADP-dependent phosphogluconate dehydrogenase.	0
NZ_CP019636.1\|WP_087538986.1\|2056357_2057869_+\|aldehyde-dehydrogenase-family-protein	gnl\|CDD\|143410	cd07091, ALDH_F1-2_Ald2-like, ALDH subfamily: ALDH families 1and 2, including 10-formyltetrahydrofolate dehydrogenase, NAD+-dependent retinal dehydrogenase 1 and related proteins. ALDH subfamily which includes the NAD+-dependent retinal dehydrogenase 1 (RALDH 1, ALDH1, EC=1.2.1.36), also known as aldehyde dehydrogenase family 1 member A1 (ALDH1A1), in humans, a homotetrameric, cytosolic enzyme that catalyzes the oxidation of retinaldehyde to retinoic acid. Human ALDH1B1 and ALDH2 are also in this cluster; both are mitochrondrial homotetramers which play important roles in acetaldehyde oxidation; ALDH1B1 in response to UV light exposure and ALDH2 during ethanol metabolism. 10-formyltetrahydrofolate dehydrogenase (FTHFDH, EC=1.5.1.6), also known as aldehyde dehydrogenase family 1 member L1 (ALDH1L1), in humans, a multi-domain homotetramer with an N-terminal formyl transferase domain and a C-terminal ALDH domain. FTHFDH catalyzes an NADP+-dependent dehydrogenase reaction resulting in the conversion of 10-formyltetrahydrofolate to tetrahydrofolate and CO2. Also included in this subfamily is the Arabidosis aldehyde dehydrogenase family 2 members B4 and B7 (EC=1.2.1.3), which are mitochondrial, homotetramers that oxidize acetaldehyde and glycolaldehyde, as well as, the Arabidosis cytosolic, homotetramer ALDH2C4 (EC=1.2.1.3), an enzyme involved in the oxidation of sinapalehyde and coniferaldehyde. Also included is the AldA aldehyde dehydrogenase of Aspergillus nidulans (locus AN0554), the aldehyde dehydrogenase 2 (YMR170c, ALD5, EC=1.2.1.5) of Saccharomyces cerevisiae, and other similar sequences.	0
NZ_CP019636.1\|WP_087538975.1\|2040096_2040588_-\|BON-domain-containing-protein	gnl\|CDD\|335963	pfam04972, BON, BON domain. This domain is found in a family of osmotic shock protection proteins. It is also found in some Secretins and a group of potential haemolysins. Its likely function is attachment to phospholipid membranes.	3.09733e-08
NZ_CP019636.1\|WP_087538985.1\|2054801_2055989_+\|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.	1.23601e-67
NZ_CP019636.1\|WP_087538989.1\|2060590_2060869_-\|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	gnl\|CDD\|368240	pfam05016, ParE_toxin, ParE toxin of type II toxin-antitoxin system, parDE. ParE is the toxin family of a type II toxin-antitoxin family. It is toxic towards DNA gyrase, but is neutralized by the antitoxin ParD. The family also encompasses RelE/ParE described in.	1.12472e-12
NZ_CP019636.1\|WP_087546097.1\|2060865_2061132_-\|ribbon-helix-helix-protein,-CopG-family	gnl\|CDD\|226420	COG3905, COG3905, Predicted transcriptional regulator [Transcription].	8.05247e-13
NZ_CP019636.1\|WP_087538984.1\|2052095_2054693_+\|CHAT-domain-containing-protein	gnl\|CDD\|378942	pfam12770, CHAT, CHAT domain. These proteins appear to be related to peptidases in peptidase clan CD that includes the caspases. This domain has been termed the CHAT domain for Caspase HetF Associated with Tprs. This family has been identified as a sister group to the separins.	6.58298e-19
NZ_CP019636.1\|WP_087538990.1\|2061465_2064339_+\|isoleucine--tRNA-ligase	gnl\|CDD\|215452	PLN02843, PLN02843, isoleucyl-tRNA synthetase.	0

>NZ_CP019636.1|WP_087538983.1|2049086_2049413_-|thioredoxin-family-protein
MNLAVIKFSSEDCGICHKMSFYDKKVAEELALLFIDVKMQDTTTYRKYRKILLSQYPDKSQMGWPTYIICDSPEGEFQILGEVKGGHPKGEFRTRLQEVLNSAASNQN
>NZ_CP019636.1|WP_087538982.1|2048866_2049100_+|hypothetical-protein
MSITVTGTVERRDIGTGAWALVTDEGKTYEILRGADKNLLKQGQKAKVTGQVREDVMTVAMIGPVLEVKSFDVISSD
>NZ_CP019636.1|WP_087538981.1|2046907_2048764_+|peptidase-S8
MKKLILFCLFVIGLGVALFNFINFQGLATKGEFETIVLNFREDIPKEVLQQDLQAIAQQYNVTPQLDNQFSAKENVYIIKGDKQRLKELKKSQFAQEMDFIEPNYIYKLPKPGKVTWLGEYLQPSQEVDEAKPALQGPNDPYYSKQWNLHNIHVEGAWTQTKGKDVTVAVIDTGVTRVRDLLETEFVAGYDFVNDRVEAKDDNGHGTHVAGTIAQSTNNSYGVAGIAYEAKLMPLKVLSEYGGGTVADIAEAIKFAADNGADVINMSLGGGGESQLMKDAIEYAHKKGVVIIAAAGNENQNSAAYPARYPHVIGVSALGPDGEKAPYSNFGAGVDISAPGGSDAGKILQETIDPDNNGTGVFLGFQGTSMAAPHVAGVAALVKASGVKEPDQILEVLKQSARGVQDDGLNYYGAGQLNAEAAVQVANHGQINFQDFFRWLRDNGYLNPRFWIDGGAVALLPKILMVIGSYLLAWFLRVYFPFRWGWALSTGLIAGSSGLFPLKGIFIFDLPQWPFRLLGSSIPELGNTFQGTNAFNPLFASVLIPLVLMAFLLGNPKWKWFSVGSSLGVAACLAVSAVSDPTVWGLGSGILARIFLITNALLCFGLARLAVKNEEQPA
>NZ_CP019636.1|WP_087538980.1|2046346_2046787_-|hypothetical-protein
MERGLLWLPLLFAFFWLAWQGSKEYQKIEAYRTWAEQFERAKYDIYAVLGQKGNNITWGKPTPKGPIKLETFSLLDVKQISLLIDDKQVDIERTPEKGRTIELEFLFSEPNQTVRVPFTEIPLAAEWGKCLQGQLQRIQEGTQDKV
>NZ_CP019636.1|WP_087538979.1|2045378_2046200_-|bifunctional-hydroxymethylpyrimidine-kinase/phosphomethylpyrimidine-kinase
MNAETTPKVPVALTIAGSDSGGGAGIQADLRTFAFHCIHGTSAVTCITAQNTLGVTRVDAMAPEAVVAQICAVYEDIGVQAAKTGMLLNKEIITAVAQQVEALQLHNLVVDPVMVSRTGAQLLDDDAVKTLRNLLIPKAAIVTPNRYEAQILSGLPIHSLDDMRAAAQIIHQNAAAKAVLVKGGGMQGSLRGVDIWFDGHKMETLTTKHIDTKNSHGTGCTLSAAIAANLALGKDLITAVRQAKEYVTSALSYALEIGKGQGPVGHFFPLLIK
>NZ_CP019636.1|WP_087538978.1|2044450_2045101_-|hypothetical-protein
MRTITGSVHSSTPAPNTQTYSPAVPISVYRDLAAELQAVQAKLDGLNVQNQQLVQENQVLRQEIAKAVESVLRLQKLVDAQAKVSSHQTSQAPADYRTEIKRPLTETTSHQAPADYRTEIKRPLTEATSKEQVSRPRVFYRESSPTPPFPSVMQIPVPVSEPVFIEEQDVSYTPHSESRPTQIRGWWLIIAILLIIVLGFGTGYLVVRPLFESHSR
>NZ_CP019636.1|WP_017749852.1|2043822_2044161_-|P-II-family-nitrogen-regulator
MKKVEAIIRPFKLDEVKIALVNAGIVGMTVSEVRGFGRQKGQTERYRGSEYTVEFLQKLKVEIVVEDNQVDMVVDKIIAAARTGEIGDGKIFISPVEQVVRIRTGEKNTEAV
>NZ_CP019636.1|WP_087538977.1|2041950_2043492_+|HAMP-domain-containing-histidine-kinase
MYKWILPSLSEVLANSQSTMTECSSAKAEQQWRVSVAATEQLLLNTLATALPEANLGLVLAAPAPVFSEPSLTQNLQTVTFTAKPFNPLALMPFQLPPGVAATDTFAPDESVLPVLGTDPLAREQFCLVFTKQFRLVLVLAEDTNGGKTFSFSFEPEVVELAWRALGARVILSHPDLFANLEELVQKYSPVAPDYRTIMEFSRLLLKQFPEPEEDTEIGKQGDIGTRGRAECVETVPTSPRLPTKHSALRQETPNASVLLCDSSEVPTRSDVELLQAFAHEVRTPLTTIRTITRLLLKQRDLPANVIKRLELIDHECTEQIDRMELLFRAAELETSAPVKCTNAQLTAMSLEQVLQQSIPRWQQAANRRNLTLDVVLPQQLPTVVSNPSMLDRVLTGLMENFTRSLPAGSHIQVQVIPAGDQLKLQLLPLPQVTDNSKATVSSCTPPIRKALGQLLMFQPETGTISLNLAATKHLFQAIGGKLIVRERPHHGEVLTIFLPLEVTNQQKLEVNR
>NZ_CP019636.1|WP_087538976.1|2040902_2041574_-|DUF1269-domain-containing-protein
MALGEHKRAVGVFSNRREAEHALTELRDAGFPMNKISVIAKDSDRSGDIAGVETQKHVGNKADEGAAAGAVTGATLGGITGLLVGLGTLAIPGVGPILLAGEIATTLATTIAGAGIGAAAGGLLGALIGLGIPEERARVYNERVSRGDYLVIVEGTDSDVRRAETVLRNRGIEEFGIYSAPGVVNTHTNDSARVVSNESLETHQPPVKIVDRRDTVDRRDTIV
>NZ_CP019636.1|WP_087538975.1|2040096_2040588_-|BON-domain-containing-protein
MNKFIPLIISGVIAVGAFGCGEPPSRTSADAPSGTNENVNAPTKETAQTTQQDATSEVRKDQIESDIRAREQRNNATGGDTDRADADLESEVRGKLEANLPASQLTVDAKEGDVTVAGTVPTQEQLNKIPTLAQEIKGVKSVKVNAKVAPAQPTSNTNNQPGQ
>NZ_CP019636.1|WP_087538984.1|2052095_2054693_+|CHAT-domain-containing-protein
MTQEFHISVTPVGQNDYLVRTEQVAPGVPLAEELVTWPVADWLTAAGHLMNDPLKSVLQGDAIARNSVNLVALGQQLYNALFQGTLRDSWITAQGIAQNHQQVLRLRLGLKDIRLARLPWEVMHAGDRPVATGPHIAFSRYQSGIGGASRLPSTSMPIPSEEGRIKVLMAIASPTDLVRLDLLKQEAIKLQAELHRGGEGGDYLPHIELTLLEQPGREELTQALEQGRYHVLHYSGHSNIGSNGGEIYLVSNRTGLRETLSGDDLAGLLVNNNIQMAVFNSCLGTYAATAADPTGDTGERNLTESLVKRGIRSVLAMSERIPDEVALMLTQLFYRNLSQGYPVDLCVSRMRQGLIAAYGSHQLYWALPILYLQPEFDGYLSPGMFFSQDEELFDEYGSSLKTTATIYSDPANDADLPLPLEDMLPSTLARDFSDLDLLGEETWGDLVDEIEYDDPTYAEDSAIVSDLFRQLDRQKTASEQSSMTAELVQFGEDSFDDKEVSGEIASLENDVGMWEEVRAAASYGRQLGAARNRELPSSSSELTRQEAGNLQRDWEGSNVSSLTQTTSSPSQRAAAERRKRRKLLGVVGAVGVSAIAGIVSFNWWSQNQQISRLAPVLPIPTQSQQPGSSSSSPQVNLKTADTKTVTAIASEKVSQGNLQGGLDAVEELLNRNVLPNAKAALELVPQEFIDDPSVNFFKGRLAWQAVQTGDNTYSIDDARRYWESAVKAKPDSLLYINALGFAYYVEGNLNLANDSWFKALSLAVREQNTTAVSPTTFSSSKPLPRDALTAYTGLALSLYKTAHSQPNGKRERYLNEAIKLRQMIVKNDPINFQPKELSQNWLWTEKALQDWKALLQLKSQRSAID
>NZ_CP019636.1|WP_087538985.1|2054801_2055989_+|serine/threonine-protein-kinase
MSYCLNPNCPKPLNTNDGRFCQTCGSKLLLKERYQAIKPIGQGGFGRTFLAVDEDKPSKPRCVIKQFYPQAQGTSTVQKAVELFTQEAMRLDELGKHPQIPELLAYFTQDDRQYLVQEFIDGLNLAQELAQKSAFNETQIRQLLNDLLPVLQFCHARQVIHRDIKPENIICRSTPQQTHGNLVLVDFGAAKEATYTALNRTGTSIGSPEYVAPEQIRGRAIFASDIYSLGVTCIHLLTQRSPFDVYDTHNDAWMWRQYLTSPVSNELSSILDKMLESIPVRRYQTVDEVLKDLNKGQQLAPTPAASVKQIAPSTSISTPVSINKASNQINKEFEEMQLDQELEEMKTLFLLGGKPKNKTNTPSQTQSSTSQPSSSKSKIDEELEELKAKYKNGEL
>NZ_CP019636.1|WP_087538986.1|2056357_2057869_+|aldehyde-dehydrogenase-family-protein
MPTLLEASGTHISSQVLKFLNQPLKLLIGGKWVESASGQTFPVFNPATGQIITHAASGESEDINRAVQAARQAFESGPWSRLTVSERGKLIWKLADLLEANLEEFAELESMDNGKPISVARVADVPLAVDLFRYMAGWATKIEGNTIPISVPYTPGTQYFAYTVREPVGVVGQIIPWNFPLLMAAWKLGPALAAGCTIVLKPAEQTPLSAIRLGELICEAGFPDGVINIVTGYGESAGAPLAAHPDVDKIAFTGSTEVGRLIVKAATGNLKKVSLELGGKSPNVVFKDVDPEIAIKGAANSIFFNHGQCCAAGSRLYVEQDIFEQVVEGVAAEAKKIKIGPGLNPSTEMGPLVSDEQLNRVCGYIQSGFAEGAKALAGGQRIGEQGYFVEPTVLVDTKQTMKVVQEEIFGPVVTAMPFREVDELLPLANDSAYGLAAGIWTNDLSKAHRLASKLRAGTVWINCYNVFDAALPFGGYKQSGWGRDMGHNALELYTEVKAVCAKL
>NZ_CP019636.1|WP_087538987.1|2057990_2059418_-|NADP-dependent-phosphogluconate-dehydrogenase
MTQQSFGVIGLAVMGENIALNVERNGFPIAVYNRSRDKTDKFIAERAQGRNVKAAFTLEEFVASLERPRRILIMVQAGKPVDAVIGQLKPLLDEGDIIIDGGNSWFEDTDRRTQELEPAGFRFIGMGVSGGEEGALNGPSLMPGGTQSSYQYLEPIFTKIAAQVDDGPCVTYVGPGGSGHYVKMVHNGIEYGDMQLIAEAYDLLKNAAGLDHNQLHEVFAQWNTTDELNSFLIEITANIFPYIDPDTNLPLVDLIVDSAGQKGTGRWTVQTALELGVSVPTIIAAVNGRIISSYKQERVAASKVLTGPTGKYEGNTKDFINKVRDALYCSKICSYAQGMALLSKASQTYNWNLQLGELARIWKGGCIIRAGFLNKIKNAFGENPSLPNLLLAPEFKQTILDRQTAWREVLVTAATLGIPVPAFSASLDYFDSYRRDRLPQNLTQAQRDYFGAHTYERVDKPGSFHTEWVPITEKS
>NZ_CP019636.1|WP_087538988.1|2059789_2060521_+|hypothetical-protein
MLAYILALAVGLGSVALYLAAFFFPEIHRKNDFIWSGVGLFYALVLWIFAQRITGGLLLGHVASVALLGWFGWQTLSLRRQLTPKTQQTQIPSTETVKTNLQEQVSKLSLPERLGQLQKGIGSTFSGVKDRVQTVGKKTPEKPTAEQPVVTSPSTTDIEAQRPTSEQTAEAVASAPTEAKTESVPEAVPPSPPSPELVEAAQAHTETEKTPVPIEEIAPDAELAPPAEAPPEQIPPNSSTQSS
>NZ_CP019636.1|WP_087538989.1|2060590_2060869_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin
MKLKFSESAVRDLVRLREFIAKNSPQAAERVSLRLRQAIGKLVLHPDIGRPVPELENVRELIAGDYVVRYLREEDTLFVLRVWHGKKYRDFE
>NZ_CP019636.1|WP_087546097.1|2060865_2061132_-|ribbon-helix-helix-protein,-CopG-family
MSTTSFRLDDDLEEKLEMTATKLQRTKGWIINDALRQYIAREERKLRMLEETEEAIADIQASRVVSGEEVMQWLETWGTATERKAPKA
>NZ_CP019636.1|WP_087538990.1|2061465_2064339_+|isoleucine--tRNA-ligase
MTETGKYKDTVNLPKTNFDMRANAVKREPEIQKFWEENKIYERLSQNNPGELFILHDGPPYANGSLHLGHALNKILKDIINRYQLLRGRKVRYVPGWDCHGLPIELKVLQNMKSAERQNLTPLQLRQKAKEFALSTVDEQRESFKRYGVWGDWEHPYLTLKPEYEAAQVGVFGQMVLKGYIYRGLKPVHWSPSSKTALAEAELEYPEGHISRSIYAAFPITSLSEAAKPTLGEFLPQLGVAIWTTTPWTIPGNLAVALNPSLNYAVVEVSSPVEGVGFKYLIVAADLVERLSEILGTQLTVKTTIKGKDLEHSTYRHPLFDRESPIVIGGDYVTTDSGTGLVHTAPGHGQEDYIVGQRYGLPILAPVDDNGNFTEEAGPFAGLNVLGDGNQAVIDALTAAGSLLKEEPYQHKYPYDWRTKKPTIFRATEQWFASVEGFRDEALKAIASVKWIPAQGENRITPMVAERSDWCISRQRSWGVPIPVFYDEETGEPLLNEETISHVQGIFAEKGSDAWWELPPQELLPEKYRNNGRSYRKGTDTMDVWFDSGSSWAAVAEQRPELRYPADMYLEGSDQHRGWFQSSLLTSVAVNDCAPYKTVLTHGFILDEQGRKQSKSLGNTVEPKVVIEGGKNQKEEPAYGVDVLRLWVSSVDYTSDVPLGKNILKQLTDIRNKIRNTARFLLGNLHDFDPQKDAVPFEELPQLDRYMLHRMTEVFGEVTEAFDTFQFFRFFQTIQNFCVVDLSNFYLDIAKDRLYISAPDSWRRRSCQTVLKIALENLARAIAPVLSHMAEDIWQFLPYKTPYKSVFEAGWVQLDQKWQNPELAVLWQQLRQLRTEVNKVLEEARVKKLIGSSLEAKVLLYIADEQLRSSVKALNASQNGVDELRYLFITSQVDLLDSPEAVQGLEYKLQSDTWDIGVVNAEGQKCDRCWNYSTHVGESAEHPLICERCVAALAGEF
>NZ_CP019636.1|WP_087538991.1|2064397_2065336_-|ParA-family-protein
MGYVIATANMKGGVGKTTLTVNVATCLVKNHGKRVLVLDLDSQISATLSLMSPVDFAKIRKQRRTLRYLIDDIITPSSRAKLTIQDIIQPQVCQIPGLDLLPGDIDLYDEFVVSEMLHQQAVSLGENEFETIWNRFERVLLGKILEPVRQEYDFIILDCAPGYNLLTRSALATSNFYILPAKPEPLSVVGIQLLERRIAQLKESHENEANIDISMLGIVFTMSNTNFLTGRYYKQVMQRVHQDFGDARICQIQIPVDVNVAKAVDSFTPVVVNNPSTPGSKAFYQLTQELLQKLEYAEAQKRQKANLELATP
>NZ_CP019636.1|WP_087538992.1|2065719_2066067_-|DUF86-domain-containing-protein
MKDDRLYLSNIKECIERIESYTFEGKEVFMQTLIIQDAVIRNFEIIGEATKRLSTDLKEAYPNVPWQQIAGFRDVLIHNYLKVNLNRVWGVIEQNLPELKVTVEEMLQKLEGEGT

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Crispr_ID: NZ_CP019636_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_5

2573883-2574015

Orphan

Consensus_repeat	Method
AATGCAATAGTCTGCATTGCTATTGCATCAAAATGTGAAAATGTAAGAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_5

>merge|NZ_CP019636|5|2573883-2574015|CRISPRCasFinder
AATGCAATAGTCTGCATTGCTATTGCATCAAAATGTGAAAATGTAAGATAGAAAGTGCGAAGCATAACTTATGCTACTTAAACAAATGCAATAGTCTGCATTGCTATTGCATCAAAATGTGAAAATGGAAGAT

>NZ_CP019636|5|5|2573883-2574015|CRISPRCasFinder
AATGCAATAGTCTGCATTGCTATTGCATCAAAATGTGAAAATGTAAGAT	AGAAAGTGCGAAGCATAACTTATGCTACTTAAACA
AATGCAATAGTCTGCATTGCTATTGCATCAAAATGTGAAAATGGAAGAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087539341.1\|2584873_2585512_+\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380345
NZ_CP019636.1\|WP_087539337.1\|2582335_2583505_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|130253
NZ_CP019636.1\|WP_087539324.1\|2574110_2574701_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225965
NZ_CP019636.1\|WP_087539313.1\|2568338_2569253_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP019636.1\|WP_087546124.1\|2565719_2566043_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539327.1\|2574745_2576467_-\|flavin-oxidoreductase	unknown	unknown	gnl\|CDD\|223503
NZ_CP019636.1\|WP_087539299.1\|2563368_2563677_-\|circadian-clock-protein-KaiB	unknown	unknown	gnl\|CDD\|181770
NZ_CP019636.1\|WP_087539333.1\|2579930_2580851_+\|DUF3102-domain-containing-protein	unknown	unknown	gnl\|CDD\|371455
NZ_CP019636.1\|WP_157679375.1\|2578555_2578825_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539335.1\|2581114_2582314_+\|ABC-exporter-membrane-fusion-protein	unknown	unknown	gnl\|CDD\|213754
NZ_CP019636.1\|WP_087539308.1\|2566094_2566454_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539329.1\|2576492_2578217_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|223503
NZ_CP019636.1\|WP_087539319.1\|2571478_2572081_+\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|272971
NZ_CP019636.1\|WP_087539345.1\|2586792_2587887_+\|dTDP-glucose-4,6-dehydratase	unknown	unknown	gnl\|CDD\|224013
NZ_CP019636.1\|WP_087539302.1\|2564092_2564635_-\|PadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224609
NZ_CP019636.1\|WP_087539316.1\|2569560_2570907_+\|cytochrome-P450	unknown	unknown	gnl\|CDD\|225035
NZ_CP019636.1\|WP_087539311.1\|2567076_2568066_-\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|226985
NZ_CP019636.1\|WP_087539321.1\|2572101_2572383_-\|prevent-host-death-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539343.1\|2585737_2586412_+\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP019636.1\|WP_087539305.1\|2564749_2565649_+\|pirin-family-protein	unknown	unknown	gnl\|CDD\|224655

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087539341.1\|2584873_2585512_+\|cupin-domain-containing-protein	gnl\|CDD\|380345	cd02215, cupin_QDO_N_C, quercetinase, N- and C-terminal cupin domains. This family contains quercetinase (also known as quercetin 2,3-dioxygenase, 2,3QD, QDO and YxaG; EC 1.13.11.24), a mononuclear copper-dependent dioxygenase that catalyzes the cleavage of the flavonol quercetin (5,7,3',4'-tetrahydroxyflavonol) heterocyclic ring to produce 2-protocatechuoyl-phloroglucinol carboxylic acid and carbon monoxide. Bacillus subtilis quercetin 2,3-dioxygenase (QDO) is a homodimer that shows oxygenase activity with several divalent metals such as Mn2+, Co2+, Fe2+, and Cu2+, although the preferred one appears to be Mn2+. The dioxygen binds to the metal ion of the Cu-QDO-quercetin complex, yielding a Cu2+-superoxo quercetin radical intermediate, which then forms a Cu2+-alkylperoxo complex which then evolves into endoperoxide intermediate that decomposes to the product. Quercetinase is a bicupin with two tandem cupin beta-barrel domains, both of which are included in this alignment model. The pirins, which also belong to the cupin domain family, have been shown to catalyze a reaction involving quercetin and may have a function similar to that of quercetinase.	5.43719e-11
NZ_CP019636.1\|WP_087539337.1\|2582335_2583505_+\|FtsX-like-permease-family-protein	gnl\|CDD\|130253	TIGR01185, membrane_spanning_subunit, DevC protein. This model describes a predicted membrane subunit, DevC, of an ABC transporter known so far from two species of cyanobacteria. Some experimental data from mutational analysis suggest that this protein along with DevA and DevB encoded in the same operon may be involved in the transport/export of glycolipids. [Transport and binding proteins, Other].	6.49282e-136
NZ_CP019636.1\|WP_087539311.1\|2567076_2568066_-\|Rieske-2Fe-2S-domain-containing-protein	gnl\|CDD\|226985	COG4638, HcaE, Phenylpropionate dioxygenase and related ring-hydroxylating dioxygenases, large terminal subunit [Inorganic ion transport and metabolism / General function prediction only].	2.16012e-19
NZ_CP019636.1\|WP_087539305.1\|2564749_2565649_+\|pirin-family-protein	gnl\|CDD\|224655	COG1741, COG1741, Pirin-related protein [General function prediction only].	2.03122e-74
NZ_CP019636.1\|WP_087539313.1\|2568338_2569253_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.76e-17
NZ_CP019636.1\|WP_087539333.1\|2579930_2580851_+\|DUF3102-domain-containing-protein	gnl\|CDD\|371455	pfam11300, DUF3102, Protein of unknown function (DUF3102). This family of proteins has no known function.	3.86293e-07
NZ_CP019636.1\|WP_087539327.1\|2574745_2576467_-\|flavin-oxidoreductase	gnl\|CDD\|223503	COG0426, FpaA, Uncharacterized flavoproteins [Energy production and conversion].	1.76523e-170
NZ_CP019636.1\|WP_087539299.1\|2563368_2563677_-\|circadian-clock-protein-KaiB	gnl\|CDD\|181770	PRK09301, PRK09301, circadian clock protein KaiB; Provisional.	5.49971e-24
NZ_CP019636.1\|WP_087539324.1\|2574110_2574701_-\|hypothetical-protein	gnl\|CDD\|225965	COG3431, COG3431, Predicted membrane protein [Function unknown].	2.20301e-35
NZ_CP019636.1\|WP_087539335.1\|2581114_2582314_+\|ABC-exporter-membrane-fusion-protein	gnl\|CDD\|213754	TIGR02971, devB-like_secretion_protein, ABC exporter membrane fusion protein, DevB family. Members of this protein family are found mostly in the Cyanobacteria, but also in the Planctomycetes. DevB from Anabaena sp. strain PCC 7120 is partially characterized as a membrane fusion protein of the DevBCA ABC exporter, probably a glycolipid exporter, required for heterocyst formation. Most Cyanobacteria have one member only, but Nostoc sp. PCC 7120 has seven members.	1.08097e-90
NZ_CP019636.1\|WP_087539319.1\|2571478_2572081_+\|PAS-domain-S-box-protein	gnl\|CDD\|272971	TIGR00229, Sensor_protein_FixL, PAS domain S-box. The PAS domain was previously described. This sensory box, or S-box domain occupies the central portion of the PAS domain but is more widely distributed. It is often tandemly repeated. Known prosthetic groups bound in the S-box domain include heme in the oxygen sensor FixL, FAD in the redox potential sensor NifL, and a 4-hydroxycinnamyl chromophore in photoactive yellow protein. Proteins containing the domain often contain other regulatory domains such as response regulator or sensor histidine kinase domains. Other S-box proteins include phytochromes and the aryl hydrocarbon receptor nuclear translocator. [Regulatory functions, Small molecule interactions].	2.9081e-09
NZ_CP019636.1\|WP_087539345.1\|2586792_2587887_+\|dTDP-glucose-4,6-dehydratase	gnl\|CDD\|224013	COG1088, RfbB, dTDP-D-glucose 4,6-dehydratase [Cell envelope biogenesis, outer membrane].	0
NZ_CP019636.1\|WP_087539302.1\|2564092_2564635_-\|PadR-family-transcriptional-regulator	gnl\|CDD\|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	1.6263e-21
NZ_CP019636.1\|WP_087539316.1\|2569560_2570907_+\|cytochrome-P450	gnl\|CDD\|225035	COG2124, CypX, Cytochrome P450 [Secondary metabolites biosynthesis, transport, and catabolism].	6.8262e-96
NZ_CP019636.1\|WP_087539343.1\|2585737_2586412_+\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	2.7082e-41
NZ_CP019636.1\|WP_087539329.1\|2576492_2578217_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|223503	COG0426, FpaA, Uncharacterized flavoproteins [Energy production and conversion].	2.08961e-175

>NZ_CP019636.1|WP_087539321.1|2572101_2572383_-|prevent-host-death-protein
MKWTLEEAQKQLPSVINATSLEPQLIYTEEELVAAIVDPELFSEFLNWRQKAAKTSLAQVFKELQQLCSEENYSLEIPLRSDRDNPFTEDKDE
>NZ_CP019636.1|WP_087539319.1|2571478_2572081_+|PAS-domain-S-box-protein
MQEIYLAESVQLYPTLQLPIVRSLAGETVHVDNLELHQQNKIIPLEVLSTPIFDEFGKIVYAIAAFIDITERKQAQKLLTDYNSILEQQVAERTLELQQEIAERKQAEQALIESETRFRLLAEATFEAIAITEKGILLDSNQACAEMFSYDLSEVIGMHIMDFTAPEYREEVMQKILSGDEVQYRSMLSLLDSESVELIH
>NZ_CP019636.1|WP_087539316.1|2569560_2570907_+|cytochrome-P450
MVQKKQPEGPQTPALLQILQWSTRPLEFMETCAKRYGDCFTVKLGGSTPYVFFSNPQAIEKIFTTAPNLFGVYSILRPTVGDNSLIILEGDRHHQQRQLLMPPFHGERMRAYGQLIFQIAEKVTSQWTKGAEVTIRPFMQEISLDIILQAVFGLNQGERSQQLKPLLISLLNLTTSPLMFALAFFPALIKDLGPLSPGRYFVQRKQKIDQLIYAEIHERREKLDPSRSDILTLLMSARDEAGQPMTDQELRDELITLLLAGHETTALGLTWALYWIHSLPTVKEKLLKELDTLGSDLDPNTITRLPYLNAVCSETLRIYPILLQTVPRVVKSPMHFMGYEFEPGTFLSPCIYLTHRRQDLYPEPEQFKPERFLERQFSPYEYLPFGGGNRRCIGAAFSLYEIKLVLATILSRFELALAESGPVRPVRRGVAMAPASGVKMVFKGERQN
>NZ_CP019636.1|WP_087539313.1|2568338_2569253_+|TetR/AcrR-family-transcriptional-regulator
MNSPTKKNASMRRQPKQKRSQQRVERILDAAAEVFDEMGYEATTTHAIAARADTAIGSLYQFFPDKLAIFHALELRHVERVHAVWAKLSQPEIIQLPFEPFIRTLGAAFQQLFKQPTCRIVFVQYFTSRAIFQNIDDSFTEEAIDFMAKLLQERNPALSTEHCHLLAQVCTHAYNTLLLLALRSDETHRQEIFEQMEALLSAYLRPHVGDKVLHNKVMKVMKCPHCEGERISKNGHRHGKQRYICKDCGKQFPEAYSLQGYADEVKQQCLELYRDGVSFREIERKTGVSHNTVIHWVKHTHTNC
>NZ_CP019636.1|WP_087539311.1|2567076_2568066_-|Rieske-2Fe-2S-domain-containing-protein
MSMLAGAPWLLAHKSMLEVNKPKKVSLYGTDYVLWQEKTGKVNALPNACPHMGAMLSEGWCQEREDKSSTVICPFHALEFDGEGCTVLPGSKKKTLPQLKPLELIIQGDFIWSYGGFEPKIPIPNILNEIASKYEFIGHTADTSVETDLLSMLLVMHDYNHQNGTHRPLFRIEEVRFETFEDNGHHSHAFYSMPTAPASLSEKLKKPDLLLIPKVLKAHLENYFPSLVIFHGEIGLGKVAQIHLFVPESKTRTRTYILMYGIAKNPVFKPLGQTFLNFAKVVVEQDSDILRKIYPNTPQKIKLNNEVGMDWVRRNFESWPEIVTPNLSK
>NZ_CP019636.1|WP_087539308.1|2566094_2566454_-|hypothetical-protein
MLNKTFIVGILSVATLGIVSLPVQAEQTSTQGSNQTATITGNNNQINQYIIQVNVQKNRGNWKGKHQPSQPQQSSSQGATQSAEAVGDGNQINQDIQQVNDQQQNVHSGSHGRGRGHKK
>NZ_CP019636.1|WP_087546124.1|2565719_2566043_+|hypothetical-protein
MLKIERNTYEQVHGRVSSGELLQLVIHHEQFAWLRQLSMLVVQIDEMLQADEPVSLDDAHSLIADARTLLTPQEDGNAFEKNYYNALQREPAAVLAHAEVTKLLEKN
>NZ_CP019636.1|WP_087539305.1|2564749_2565649_+|pirin-family-protein
MTSVHLSKEQRTVAGIISSVETLEGEGMVVRRPFPKSTFSDFDPFLLLDELGPVKVEPNQAKGAPDHPHRGFETVTYLLAGRLEHKDSYGHTGTLSPGDVQWMTAGAGIVHSEVPEREFGRTGGRLHALQLWVNLPSRDKLMPPRYQEISASRIPIAQTDDGSVTVKIIAGSALGVSAVIETRTPIIYLHFTLQPGATVVQPVPRDYNTFAYVLEGEGMFGAESERGLDGQMVLFAQDGEDVTITNPVDAIAPLEVLLIGGIPLNEPVVRYGPFVMNTEDEIVQAFADYRNGRMGTIHV
>NZ_CP019636.1|WP_087539302.1|2564092_2564635_-|PadR-family-transcriptional-regulator
MSLAHTILGLLHQQQMSGYDLKTICFDQTIAHLWQADQAQIYRTLDKLEERGWVSCQVEIQRDRPNRKVYRVTEAGKTELVRWLGSPQPLPTVRDPLLIQMFFAAVLPNDAVIPLLEQQLAARRQKLAECEAIKIPPLDDASASREQQMQRLGLELVIRQEQTYIDWLDMAIQVIRGQTL
>NZ_CP019636.1|WP_087539299.1|2563368_2563677_-|circadian-clock-protein-KaiB
MSDKYLLKLYITGYTPRSQRAISNLIQLCESQLRNKHEIVIIDVLEQPQVAESEKILVTPTLIKEFPLPKVRIIGDLSDTKTVLLGLNIPQKNRDILSDTNQ
>NZ_CP019636.1|WP_087539324.1|2574110_2574701_-|hypothetical-protein
MQEPLEKPSTNRYAWLNTCLNRNSLVRCLEAIQDLLVISLCIGLFSFMTIQLRAMFYSLLPPLNFQVVTSDILFLLILVELFRLLIIYLQEQRISIGVAVEVSIVSVLREVIVRGVLEAHWTQILASCAFLLVMAVLLVVRVWLPPTFNGIDPERRISIRNKILAADPSSESNEHIDSQAMASILAEANNRVRSEH
>NZ_CP019636.1|WP_087539327.1|2574745_2576467_-|flavin-oxidoreductase
MTYTKLRDVQVASIGTDTTVLRSRTWDRLKFEVEYSLQKGTTANSYLIQAEKTAILDPPGESFTEIYLRELQQHLDLRYLDYVILGHVNPNRCVTLKALLEFAPQITFICSKAGAVALRIAFPERELRINVARGDEVLDLGQGHKLQFITVPTPRWPDELYTYDQQTRILFTDKLFGTHICGDEIFDEGWKRLDEDRRHYYDCLHAAQFRQVEIALDKFTPLSVNFYAPGHGPLVRYSKSRLTHDYRQWNQQQKDKDLTVALIYASAYGNTATLAQAIAKGISKSGVGVELINCEFTHPTEIQALVEKCDGFIIGSPTLGGHMPTQVQTALGIVLSIAAKSKLAGVFGSYGWSGEAVDEIETKLQSAGYHFGFDTIRVKFKPTDVILQQCKEAGTDFAQALKKAKKIRAPRQPVSDSQIDRTEQAMGRIIGPLCVVTAKRGDLSSAMLASWITQSSFNPPGLTVAVAKDRAIESLMHTGENFVLNILKEGMNLRRHFLQPFTPGQDRFVGLATQTAENGCPILSDALAYLDCTVNSRMDCGDHWVVYATVNNGQMLQVAGMTAMHHRKSGSQY
>NZ_CP019636.1|WP_087539329.1|2576492_2578217_-|MBL-fold-metallo-hydrolase
MIALAEQGQRRLTMQSIEMIPGTTAIRCLDWDRDRFDIEFGLQNGTTYNSFLIKSEKTALIDTSHEKFRQLYLDTLLELIDPAKLDYLIVSHTEPDHSGLVKELLALAPQVTVVASKVAIQFLENWVHQPFKQLIVKNGDRLDLGNGHILEFVIAPNLHWPDTIFTYDTKTQILYTCDAFGMHYCDDHTFDEDLDLIEEDFQYYYDCLMRPNARSVLSALKRMSELPIATIATGHGPLLHHNVTELVDRYRQWSQEQAKAETTVAVFYMSDYGYSDRLSQAIAHGITKTGVAVEMMDLKSADPQDVRELVSIASGLVIGTPSMTGSTAASAQAAISTILAAAKAKQLIGVFESGGRDSESVYLLFNQFRDLGLTPAFSPIVLKETPNDATYHLCEEAGTDMGQSLSRDRNIKQIKAINSELEKALGRLSSGLYILTTQKGNLSSAMLASWVAQASFKPLGITVVVARDRAIESLLHPGDCFVLNVLEEGNYQRLMKHFLQRFSPGADRFEGVKTYSANNGCPILADALAYLECEVKSRMECGDHWTIYATVSVGRVSKPDALTAVHHRKVGNHY
>NZ_CP019636.1|WP_157679375.1|2578555_2578825_+|hypothetical-protein
MQRHYLKGISLRGTQATAERVPQHKGASRTGRTFRLERTGVKWRFPDLGIRRWKPSWSTVVSFGKAPSSELLAVSPRPVCLSEAENDAT
>NZ_CP019636.1|WP_087539333.1|2579930_2580851_+|DUF3102-domain-containing-protein
MNQSVSLSVSLQQISPEQTSDFDYSALDTVTYMAVQQYTSEIKALMRRSAQDVIELGQKLIEVKQHLGHGNFRKWLKSEFNWSISTATKFMQVGEQFKCVNFTHLKITASALYLLAAPSTPPEARAEALENARCGENMTYTKAKDIVLRYKKVVLSNLDKTDIVDVAVQSANSESFQSLKPMQHQASDTCFAPEVLATEVETQTYLLSTEDSNQQIAISSKRDKDELDDTIETSASMLNQATITDNTLDALTIEIANRISNWTPEQLALVINKCVNDVLSDEDLELVITQAQQALQQRQQLRNSMS
>NZ_CP019636.1|WP_087539335.1|2581114_2582314_+|ABC-exporter-membrane-fusion-protein
MNLQILFKRSHRWTFALIVAVGTIAGTTAFYKISQLKKTSKATTVAQAPPTIRQITALGRLEPITEVIKLSIPATLSNDRVMKLMVQRGDRIKAGQVIAIMDAQARLQDALLEAQAQVKVSQANLAKVKAGAKSGEITAQQAEIVRIQQQLKGEIASQQATIDRWQTEVRTADADYNRYLSLYKEGATSASELDRKRLAQETAQAQLNEAKAKQDQSAETLQEQIRQAKATLDKIAEVRPVDVQEAQAEVEKAIATVQKAKAELAEAYIRAPITGRILNIYAKPGEVVGEKGITDLGQTDQMQVVAEVYKTDINKVREGQQAIITSESFPGQVRGSVRLIGLQVLQQEITSGKPGENLDRKVIEVRIRLNPEDSQRVANLTNLQVQVAIQPNVPLANSR
>NZ_CP019636.1|WP_087539337.1|2582335_2583505_+|FtsX-like-permease-family-protein
MLLKLFRKTPLAWLQMSRQKTRLLVATAGIAFADLLMFVQLGFQDALNDSQLNFYTKLQGDLFLVNKLSDNLTSFKNFSRDNLYQAAGINGVASVGSLYTAQVTWRNPENQSSRLIQIYGIDPSQPAFKMPEVNQHLDELKLLNRALFDKAGGLPKLGDIPTLLKKENPLSVQINNFEIQIVGLFALGSSFAAQGSVITSDSTFLRLFPERQADRIDVGIVKVKSNATLKQIQADLQAIMPDDLLVLTLDEFSARERDYWTKDSPIGVIFGLGVVLGFLVGIVIVYQILYTDISNHLPEYATLKAMGYSELYFIGVVIQEALIFAALGFVPGFLLSTGLYTITQSATLLPIAMKLSRATLVLVLTIIMCIGAGAIALQKLQQADPADIF
>NZ_CP019636.1|WP_087539341.1|2584873_2585512_+|cupin-domain-containing-protein
MVLNQQNSHSSDTWLAATKESSTEASTSLSQPEPIQNPVTGECLTVLCSTRDSDGERLLLCFDLPPKTKGAPLHYHLTITETFEVLNGELEMELSEKRNRKTLRPGEVIPVPPGMHHSFWNASDEWVTFTTLVQPAAEFEKFIRGMYSMARDGVSANFLQFALLVEKSDSILVNKPLFVQKLISGVLTPIAYLLRVEQSLSKYWSEVDRTEA
>NZ_CP019636.1|WP_087539343.1|2585737_2586412_+|acyltransferase
MTVQELNTNTNEQAPELPAFSIVHTIITNLFAWIPHPIGALLRQLAYRFIFARIGKAVYIESGVDLLGANLIEVGNEVVMARDVRLIVTPNSLLRVGNKVCLNRGLDLSTIGSNCLIEIGDGSYIGSYVCIAGPGNIKIGKNCLIASHTGIYANNHREYGLSREGIEIQDNCWIGSGVSVLDGVTIGQGSVIGAGSVVTKDIPPYSVAVGVPAKVIKSSKGGVA
>NZ_CP019636.1|WP_087539345.1|2586792_2587887_+|dTDP-glucose-4,6-dehydratase
MQTFLVTGGIGFIGSNFILKASKERWANIINLDKLTYASNPQTLIQLQDSPGYHFVRGDIGDAELLSHLLKQYQPDAIINFAAESHVDRSIVSPQDFIQTNVVGTFQLLEASRAYWEKLSPQKREQFRFLHVSTDEVYGSLGPTDPAFREDTPYAPNSPYAASKAGSDHLVRAYYHTYGFPTLITNCSNNYGPRQFPEKLIPLIILNALHSKPLPIYGDGQNIRDWLYVVDHCQALYLVLQHSQIGESYNIGGNNEQTNLTVVEKICAILDELVPKPNFNYSSLMTFVKDRPGHDRRYAIDCSKISRELGFEPKEDFNSGLLKTIQWYLSHPTWVEQVQSGAYQTWIKQNYQDRIKVPSPRARS

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Crispr_ID: NZ_CP019636_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_6

2745823-2745921

Orphan

Consensus_repeat	Method
AACACTATGTTCAATTGATGAAGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_6

>merge|NZ_CP019636|6|2745823-2745921|CRISPRCasFinder
AACACTATGTTCAATTGATGAAGGCAGAACAATTAGGCATATAATAGGTTAACCAAATGAGCGATAATAACGAACAACGCTATGTTCAATTGATGAAGG

>NZ_CP019636|6|6|2745823-2745921|CRISPRCasFinder
AACACTATGTTCAATTGATGAAGG	CAGAACAATTAGGCATATAATAGGTTAACCAAATGAGCGATAATAACGAAC
AACGCTATGTTCAATTGATGAAGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087539600.1\|2755787_2756783_-\|J-domain-containing-protein	unknown	unknown	gnl\|CDD\|237667
NZ_CP019636.1\|WP_087539588.1\|2733607_2740045_+\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP019636.1\|WP_157679391.1\|2750124_2750268_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539592.1\|2749261_2750014_+\|thioesterase	unknown	unknown	gnl\|CDD\|225749
NZ_CP019636.1\|WP_087539594.1\|2751156_2752515_+\|MATE-family-efflux-transporter	unknown	unknown	gnl\|CDD\|240541
NZ_CP019636.1\|WP_157679393.1\|2750678_2750822_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539604.1\|2757982_2758558_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_157679395.1\|2755340_2755484_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539582.1\|2730349_2731495_+\|acyl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|173847
NZ_CP019636.1\|WP_157679387.1\|2723561_2723966_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087539576.1\|2725368_2725917_+\|Hsp20/alpha-crystallin-family-protein	unknown	unknown	gnl\|CDD\|223149
NZ_CP019636.1\|WP_087539584.1\|2731507_2733124_+\|amino-acid-adenylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|341253
NZ_CP019636.1\|WP_087539596.1\|2752651_2753047_-\|IS200/IS605-family-transposase	unknown	unknown	gnl\|CDD\|376616
NZ_CP019636.1\|WP_087539590.1\|2740046_2745662_+\|type-I-polyketide-synthase	unknown	unknown	gnl\|CDD\|225858
NZ_CP019636.1\|WP_087539571.1\|2722318_2723497_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|226925
NZ_CP019636.1\|WP_087539598.1\|2755491_2755791_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|338835
NZ_CP019636.1\|WP_087539602.1\|2756858_2757695_-\|DUF2382-domain-containing-protein	unknown	unknown	gnl\|CDD\|226379
NZ_CP019636.1\|WP_087539578.1\|2726133_2727849_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|226651
NZ_CP019636.1\|WP_087539580.1\|2729360_2730086_+\|lipocalin-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|372819
NZ_CP019636.1\|WP_087539586.1\|2733141_2733405_+\|acyl-carrier-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087539600.1\|2755787_2756783_-\|J-domain-containing-protein	gnl\|CDD\|237667	PRK14299, PRK14299, chaperone protein DnaJ; Provisional.	4.34839e-77
NZ_CP019636.1\|WP_087539588.1\|2733607_2740045_+\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP019636.1\|WP_087539592.1\|2749261_2750014_+\|thioesterase	gnl\|CDD\|225749	COG3208, GrsT, Predicted thioesterase involved in non-ribosomal peptide biosynthesis [Secondary metabolites biosynthesis, transport, and catabolism].	2.95644e-90
NZ_CP019636.1\|WP_087539582.1\|2730349_2731495_+\|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.	2.04137e-113
NZ_CP019636.1\|WP_087539594.1\|2751156_2752515_+\|MATE-family-efflux-transporter	gnl\|CDD\|240541	cd13136, MATE_DinF_like, DinF and similar proteins, a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Escherichia coli DinF is a membrane protein that has been found to protect cells against oxidative stress and bile salts. The expression of DinF is regulated as part of the SOS system. It may act by detoxifying oxidizing molecules that have the potential to damage DNA. Some member of this family have been reported to enhance the virulence of plant pathogenic bacteria by enhancing their ability to grow in the presence of toxic compounds. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).	3.54018e-97
NZ_CP019636.1\|WP_087539576.1\|2725368_2725917_+\|Hsp20/alpha-crystallin-family-protein	gnl\|CDD\|223149	COG0071, IbpA, Molecular chaperone (small heat shock protein) [Posttranslational modification, protein turnover, chaperones].	4.40171e-32
NZ_CP019636.1\|WP_087539584.1\|2731507_2733124_+\|amino-acid-adenylation-domain-containing-protein	gnl\|CDD\|341253	cd05930, A_NRPS, The adenylation domain of nonribosomal peptide synthetases (NRPS). The adenylation (A) domain of NRPS recognizes a specific amino acid or hydroxy acid and activates it as an (amino) acyl adenylate by hydrolysis of ATP. The activated acyl moiety then forms a thioester bond to the enzyme-bound cofactor phosphopantetheine of a peptidyl carrier protein domain. NRPSs are large multifunctional enzymes which synthesize many therapeutically useful peptides in bacteria and fungi via a template-directed, nucleic acid independent nonribosomal mechanism. These natural products include antibiotics, immunosuppressants, plant and animal toxins, and enzyme inhibitors. NRPS has a distinct modular structure in which each module is responsible for the recognition, activation, and in some cases, modification of a single amino acid residue of the final peptide product. The modules can be subdivided into domains that catalyze specific biochemical reactions.	5.7093e-162
NZ_CP019636.1\|WP_087539596.1\|2752651_2753047_-\|IS200/IS605-family-transposase	gnl\|CDD\|376616	pfam01797, Y1_Tnp, Transposase IS200 like. Transposases are needed for efficient transposition of the insertion sequence or transposon DNA. This family includes transposases for IS200 from E. coli.	2.03154e-49
NZ_CP019636.1\|WP_087539590.1\|2740046_2745662_+\|type-I-polyketide-synthase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP019636.1\|WP_087539571.1\|2722318_2723497_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|226925	COG4552, Eis, Predicted acetyltransferase involved in intracellular survival and related acetyltransferases [General function prediction only].	1.5586e-114
NZ_CP019636.1\|WP_087539598.1\|2755491_2755791_-\|hypothetical-protein	gnl\|CDD\|338835	pfam13591, MerR_2, MerR HTH family regulatory protein.	1.98302e-10
NZ_CP019636.1\|WP_087539602.1\|2756858_2757695_-\|DUF2382-domain-containing-protein	gnl\|CDD\|226379	COG3861, COG3861, Uncharacterized protein conserved in bacteria [Function unknown].	1.08613e-56
NZ_CP019636.1\|WP_087539580.1\|2729360_2730086_+\|lipocalin-like-domain-containing-protein	gnl\|CDD\|372819	pfam13924, Lipocalin_5, Lipocalin-like domain. This family includes domains distantly related to lipocalins. However, they do contain the important GXW motif in the first strand. The protein in this family include aln5, which is involved in biosynthesis of alnumycin. The family also includes the ZFK protein from Trypanosoma brucei which is a protein kinase. This domain is at the C-terminus of that protein. The domain is also found as the C-terminal domain in StiJ a protein involved in producing stigmatellin. This domain has been assumed to catalyze a final cyclisation reaction.	6.56375e-47
NZ_CP019636.1\|WP_087539578.1\|2726133_2727849_+\|alpha/beta-hydrolase	gnl\|CDD\|226651	COG4188, COG4188, Predicted dienelactone hydrolase [General function prediction only].	5.04982e-81

>NZ_CP019636.1|WP_087539590.1|2740046_2745662_+|type-I-polyketide-synthase
MIQIPAKPTTLQLINALEEARSKLEAVQQAKEEPIAVIGMSCRFPGAKNTESFWHLLSNGVDAIREVPANRWQIDACYDPNPDAPGKMYSRYGGFLSEVDKFDAHFFGISPREAMSLDPQQRLLLEVSFEALENGGQSSEKLFGTPTGVFIAISTFDYAMRLSEARSQIDAHLGTGTLLSPAAGRLSYSLGLRGASMVVDTACSSSLVAVHLAVNSLRNKESELALVGGVNLLLAPSLSINFSKARMLAPDGRCKTFDASANGYVRSEGCGVVVLKRLSQAIRDGDNILALIRGSAINQDGASGGLTVPSGPSQEAVVRQALKNAGVKPKEVSYIEAHGTGTSLGDPIEANALGSVFSDREEPLLVGSVKTNIGHPEAAAGVAGLIKVILCLQHKQIPPHLHLNKPNPYIPWEQLPIKVPNELMPWSTVNQQRFAGVSSFGFSGTNAHVVLSEAPAVTPKTEPETWKRPLHLLTLSAKTKPALEQMVHNYSQHLATHPNLEWADVCYTTNTRRTHFQERLAILADSVSVAQEKLLAYQAGAEDNHVFSGSKSESQPQIAFVFTGQGSQYLGMGRELYATQPTFRQALDRCQEILHEIGNQERSLLSVLYQNDDISLLEQTAYTQPTLFALEYALAQMWKSWGIEPTAVMGHSVGEYVAATVAGIFSLEDGLKLIAARGRLMQKLSGNGEMVSLLASAAQVAQAIKDNDLVSIAAINGPESTVISGEREAVRTVVAELEQKGIKTKRLKVSHAFHSALMQPMVAEFRQVVKQVTFHQPKLNFISNVTGAQERVLPTNPEYWVEHVLKPVRFASGMEALHRQGVEIFVEMGPAPILLGMGRQCLPSDYGTWLPTLHPEQSDWQGLLQALGQLYVRGVAVDWAAFHRDYAHRQVDVPTYPWQRERYWIEVAQTQPLRESGTQNGHHPLLGQRIRSAALKNQQIVFESQISADFPAYLADHRLYEKVIYPTAAYVEMVLAAGAQIFAPGMGDNHPPLVVEEFLIEQPLVLDATEATPVQLVLTPNESGYDFAIFSRKNSDNFDDHETWTRHVQGYLLTGEVPAAKAPLDLIALKQKINQEIEVESYYQKFRDVGVEYGPYFQVIEKLWCSQGDSVEVLGKIKLPEMVESNTKDSLHPLLLDGCLQLLAAALEDSPDSETKTYFLVVLERLNFFTQPGTSIWCHIHQSSHQSSSLLSSFDIHLVDENGIAVAELINLQVRRANQTALLANQTDDWLYRIAWEVKPHISAKSSSFATTDNKKSKAGSWLIFSDGGEVSSSLADLLNKQGEHCIFVSQGSSFSVLNDDRYQINPAEPKDFQNLLSAIVKKEQSVCRGIVYLWGFDRKLEMSDVPTTALDLCTNVLYLVQALSKIPPHHWGKKIPRLCLVTRDAQAVTKTSLQVQQSPLWGLARVIVLENPELETVCIDLSSHQVNEIEMLLEEILFPEQEEQVAFRDGERYVARLKHADAKTISHSAKIDSSGSYLITGGLGALGLQVANSLVEQGARHLLLVGRQGAVSPEAQAGVKQLENKGALVKIVKTDISQPDSVATLIAETDIPLRGVVHVAGVLDDGMLRDQTQERFSKVMAPKVQGAWNLHQLTKEMPLDFFVCFSSMTSVLGALGQGNYAAANAFMDALCHHRHALGLPGVSINWGPWATSGMATRLDANLQSRWDAMGFGMISPSQGMHLFANLLNGKAPQVGAMPINWSKYTVESTFLTDFHKPKEQKKEQEKTSLNFLETVKAAEKDQRQALLVAHVQSQVSKVLGYQKERVFSVSEGFFDLGMSSLTSVELRNNLQNSLGCRLPATLTFDYPTVKKLVDYLMAEFLEEADEDEELSEQSFQIDNKALKFEPLAENDDAEEIAKQFAEQLGIQWAN
>NZ_CP019636.1|WP_087539588.1|2733607_2740045_+|type-I-polyketide-synthase
MNKIAYPNHESDFAENSQQEPIAIVGMGCRFPGKADTPEAFWELLRNGVNAVTDIPSSRWDLERYYDPSPAPGKFYVRSAAFLDTNEIEQFDAEFFRMASREAASLDPQQRLLLEVSWEALEHAGIAPTSLAGSQTGVFVGIHWDDYSAERFYMVNPGEINAYPTLSNLRSLSAGRIAYVLDLHGPTMQVDTACSSALVSVHLGCQSLQNRECNLAIAGGVSLLLSPKLTVGFCQMKVLAKDGRCKTFSDSVDGFVQGEGCGVVILKRLSDALRDRDPILATIRGSVINHDGYSLTLTTPASAAQEAMLRQALGNARIEPKQVQFVETHGTGTPLGDPIEVIALAKVLGQDRQDPLVIGSMKTNMGHLGAAAGVASLMKVVLSLQHNHIPPNLHFEKPNPRIPWQKLPVTVPTELTPWPEHETKLAGVSAFGMSGTNAHVIVEAAPQLPQGELSTGGIEPLCHLLTLSAKSEKALNDLVHRYLTFLDKTEDSLANICYTAATGRSHFAHRLALIANSKENINEQLDAFVKGEKIIGTIQGDAYQGTPKIAFLFTGQGAQYVEMGRELYETQPAFRQALQQCDEILRSYLDRPLLSILYPDRPEDIIDLTAYTQPAMFSFEYALAELWKSWGIIPDVVMGHSVGEYVAACVAGVFSLEDGLKLIATRGRLIQQLPQEAGKMVSFIASEDLIESAIAPYATQVSVAAVNGPQSIVISGDSSSIDSIVAELKTKQIKTHELTVSHAFHSPLMEPVLKPFAQVAAQVAYSVPKIPLISNITGDQITDDVATPEYWVRHIRQPVRFADGMNTLQKMGIECFVEIGPKPILLGMGVSCLVDEEKRLVWLPSIRPSAESSTITESLAQLYVRGVDINWQGLFLDKHRRKVVLPTYPFQKERCWVDVRHERVARKSSEISAHPLLQERIYSSVLKQGEVQFEAYLSTADLPYLAEHRAFGQAIMPASAYFEMVLAAGNQLFGNRSITFEDVVIEKALKLEEPQTVQLVLIPDQEGYSWQIFSLVFINEEPTWTRYAAGKIRIGKDIPTLERNADLTTLQAGLQEHKDIKAFYQQVATQEMVYEGSFQSVRRLWRSEGEALGQIQLPKNLLNQPYHWHPALLDGCFQVLLAALPADFSETYLPVAYPHFTFWQHPTREVFSYVKLHSQPGQETLKADLQLIGKDGQIYAEAISLQLKKARSQALQQKDPWKDWLYKVVWKEVKKIAGTSDLTNKGDWLILADRTGLAETLADLLNASGQRSHLVYAKKADSRCQPEQYSVNWTDPADWRQLLASRSYHGVVYLWSLDEHDSCNSICEQILHLVQALTSAKISPQLWLVTQGAQSALKDDVVAVWQAPIWGLGKTISLEHPEFLTTCLDLPSGNHPNEAAKFLLQELLTPDAENQIAYRNGVRYVARLEPSQSTQTPTIAPVALKLTNYGTLDNLTLVPLASPSLAPDEVEIKVRASGLNFRDVLRALGMMREVEESLGIASANDILFGFECAGTIERVGKQVSGFKVGDAVIAYASGSLASVVKAKAKLVVPKPAELSFEEAATIPVTFLTAYYGLVKCAQIGPTDRVLIHNAAGGVGQAALQLAQLKGAEVFATASPPKWDFLKSLGIKHIYNSRNLEFAEQIITATNGKGVNVILNSLSGKFIDKSFDVLAQGGRFVEIGKLGIWDEQKLQALRPDAAYFPFDLGEMDGAEIIPSMLLELMTMFKEGKLKPLPAKVFPITEFVNAFRYMQQAKHIGKVVLSFQNPENCSVRQNGSYLIAGGLGALGLKVAQRLVEQGAKHLVLTGRSGVKQAANEVIKQLEHSGAKVSVINADISDQEDVKKILSECPNLRGIVHTAGVLDDGLLTEQTPMRFKKVMASKVQGAWNLHVLTQGVPLDFFVCFSSAASLVGNAGQSNYAAANAFLDALAHYRRSQGLPSLSINWGPWGEVGMAATLASRLKAQGWGIIGTEQGLQALDHLVKNEDSAQVGVLPMNWSKFLERLPENRPFFENFQTVVKPSEERPALLSQLKATLAHERRTILMEHIRSAIRNVIGLNASTRIEPRQSLFDLGLDSLMAVELRNYLEKSVECSLRSTLLFDYPTLEALVNYLLQEVLTLADISAEQTEEDQTTSTQVFEELPEEEADILLASKYEELSKLLGNI
>NZ_CP019636.1|WP_087539586.1|2733141_2733405_+|acyl-carrier-protein
MTEEQIEQMLKDFIIQELAYDQTNLVLTNNLKIIEQRVVDSMDIFRLVRFVEEEIGIFWEPEELVLKNFETIDHIKAYILRKLALEV
>NZ_CP019636.1|WP_087539584.1|2731507_2733124_+|amino-acid-adenylation-domain-containing-protein
MSYLLHHLLISSARTHSERVAVQHQEHTITYRQLDEISNQLANTLSYAGVGRGDRVGIYLDKSIEAVVAIFGILKAGATYVPLDPYAPVKRIAFIIKNCQIKTLISTKQKIDALGSNSLEELQSLNSVILADEDEQATQWFGKIVRWSEVLQAPCSPPPDPDLIENDLAYILYTSGSTGTPKGVMISHRASLTFVNWAYETFQVTAQDRVSNHAPFHFDLSIFDIFTTIKAGGTIVLFSAALSVFPINLAKYIATEKISIWYSVPSILTSLVLYGQLEKHTFPALRTILFAGEVFPIKYLRQLMAHIPHASYYNLYGPTETNVCTYYQVSPLDIERIESLPIGKACANTEVFVLTASNELVASGDEGELCVRGPGLMTGYWDLPEKSAQVRVPFTLHRSLGSEMIYRTGDLVKQAPDGNYIFLGRRDRMIKSRGYRIELGEIENVLYSHPRVEEAAVIPIPDNEIGNRIKAVVVARSSDKLAEAIPAELPDISVQDLKLFCAERLPKYMVPDLFEFRSSLPQTSTGKIDKVQLCQEIQ
>NZ_CP019636.1|WP_087539582.1|2730349_2731495_+|acyl-CoA-dehydrogenase
MDFAWNSQQIEFRKKVIRFAQQSLKSDLVKQDKERIFNRDAWQKSCDFGILGWPIPVRYGGQELDILTTAYALQGLGYGCKDNGLLFAMNAHMWAGEMPLLTFGSEEQKEKYLPKLCREGWIASHAATEPQAGSDIYSLKTTARKDGERYILNGHKHYVTNGSIADIFIILATVDPSLGKEGLTAFLIEKDTPGLVVSEPISTMGMRSAEVTELKLENCEVSVANRLGEEGAGLAIFNHGMEWERGFILACAVGTMERLLEQSTRYAKTHKQFGQAIGKFQLVANKLVEMKLRLENAKGYLYKVAWMKENKQMALMEASMANLYISEAWVQSCLEAIEIHGAYGYLTNTELERELRDAIGSKFYSGTSDIQRVVIAKFLGL
>NZ_CP019636.1|WP_087539580.1|2729360_2730086_+|lipocalin-like-domain-containing-protein
MDPISNKLIDGSVKRRNRGLARKNRLQRSFIQWFSGGLTAALIASGVAAIKAEASKSTGVQESSTNLKLDGTSPKQGSTPSLLGHPPYKMSDSSPSLTAQQKQIVGTWRLVSWENRDEQGKVTYPYGKDALGYLVYNADGYMCATLSKKDRPNFPGGDILAGTLEEQAKAVQTYIAYCGKYQVQPDKVVHLPDVSLFPNYIGTKQERLFKLEKGQLILTHAPELMDGKKQTPFLIWERASK
>NZ_CP019636.1|WP_087539578.1|2726133_2727849_+|alpha/beta-hydrolase
MNCSLMSPVIPRVIRLHFHALFCSKQSFLLHLALGCLSIGLIPTLAARPSLSAERLTISYGIAARSISINSLETYAKTGKVDDNLAAYVQYADKEQLSQLRQVLLTPIPLNAVSVSQFLYTPIGTRLLENFGEVIQQESGISGFYAIRAALILAAADPEGLTLLNVLRKFPSRAIAIDLVRSLEIAGAFQNLVNKTQQAIALINKQSSLDAANTSKLDNISVADLPRLGKFRWQKQTITLNDTSRDRTFPADIYLPVVSSSPRPVIVISHGLGSDRTSFAYLAEYFASYGFVVAVPEHPGSNAQQLQALLSGRAAEVTSAREFIDRPLDIKYLLNQLSKLSQVDSTYRGRLNLDQVGVVGQSFGGYTALALAGAPIDFKQLDKNCPASPDVLNVSLLLQCLAVNLPEESTDDLFDSRVKSVIAINPVDSSILGQASLSQIKIPVMIVSSSIDTVAPALLEQIQPFTWLTTPNKYLLLINGATHFSTIAESPTSGVPVPEQVIGPTPALAQRYIRALSLPFFQTYLANDPSYRRYLSADYVNAISQEPLPLSLVESLSLQGSTASSGIFTNF
>NZ_CP019636.1|WP_087539576.1|2725368_2725917_+|Hsp20/alpha-crystallin-family-protein
MVLSRWQPLREMNSLQRQMNRLFERLMSTEETDFITDESLFVPVAEIHEAPDHIALRVEIPGVNPDDLDVKVTPEAVLITGERKSEIREEDRGRIRSEFRYGRFQRMIPLPSRVQNDKVEAEFNNGILLLRLPKSEEEQKRIVSVRVGAGAQGQQGQISTGQQEQSTAESVSTSPQDKSQPS
>NZ_CP019636.1|WP_157679387.1|2723561_2723966_-|hypothetical-protein
MLAAGTIASTLDGAGIGSAAGSLAATLGGLDIPQEDARNYSNWIERGEYLVIIEGTDDEINRATSVLRNQNIRNWNIYEIDGARSDYPTGGYEDRTDIRPDDRPIAAAPDDQTTNLRRCVTDFVLTHPTNLLQH
>NZ_CP019636.1|WP_087539571.1|2722318_2723497_+|GNAT-family-N-acetyltransferase
MMPTFKYSQVVNQEDIQQLGNILEQCFLMSPGESEIFFNRLGLENLRIIHQGEQVAGGLVMIPMGQWWGTHRVPMTGIAGVGIAAEHRGSGAALAMMQHTVKELYAKGVPISVLYPATQRLYRKAGYEQGGAFCIWEVDTQSIQLREQPLPVIPVVPNHHEIFHDLYQQQAKLNNGHLDRHQGIWKYLIRSDEKEAVYAYLIGCADQPQGYIIFSQHQNQDGSLILLRDWTVLTTAAVQTFWSFLANYRSQIKYVQWKGSAIDSLTLLLPEQTAKQKSAKRWMLRIIDVSQALEKRGYPPEIEIELHLEVQDDLLAENNGRFILSVANGRGEVTSGGKGEMKLDIRGLAPLYTGLFTPQQLQLAGKLDATETALLAATQIFAGVSPWMADFF
>NZ_CP019636.1|WP_087539592.1|2749261_2750014_+|thioesterase
MKTEISNVWIKCSQPNPQANLRLFCLPYAGGGTSIFRLWPRELPSNVELCAIELPGRENRIGEKPISNLEILTEKLVEAFLQHLDKPFALFGHSMGALIVYELARKLQQKNVNPVYLFVSGRPAPNVPELYPPLHVLPDAEFIEKLNDIYSAIPDTVLKDKELMQLFLPVLRADMTLVETYVFSEVEPLDCPILALGGLEDHEASHDNLMTWREHTRSSFLVQMFSGGHFYLNENRQPLLQFISQTLKDY
>NZ_CP019636.1|WP_157679391.1|2750124_2750268_-|hypothetical-protein
MGSQAYLDALEQITRRAKIEALDRSIETLNQGLKDLIEETSKYRKQE
>NZ_CP019636.1|WP_157679393.1|2750678_2750822_+|hypothetical-protein
MNTWKYTFPISVEHSAKQRRCWNLGAEILVSMPLLFFVFQTRFGIWG
>NZ_CP019636.1|WP_087539594.1|2751156_2752515_+|MATE-family-efflux-transporter
MNLTFLEQYNFVPRYFRLALANVLSSIMVPLANIASVMFLGHLEEIRHFAGVNLAANLLNFVYLALFFLRMGTTGVTAQAVGRDDREGMLLVGLRNGLIALVIGLVLILLQYPLGELGFGLLNVTPEIKSSGLAYFNTQIWGAPAILLNFVLIGWFLGREKNGLVVFLSLLGNGSKIALDYLFIVHLGWESVGAGVSYAISQYLSLLVGLIFFCKEFQWVEIQAISGKIWDIAAIKSNLALNINILISNLILLFVTLTFNYEGIQMGTLVYAQNALMWQIFSFNTYFVEGLGFGTEALVGNFKGKGDSQQLLPIVVVSLSTAFVVALFFGGVCVLFPDTVFSLFTNHTEVTSNINTFLPWLQLVLVFSSIGFALEGYFLGLAQGHILRNVSSVALAVGFLPTYFFAIKFLSNHVLWLSVSLCYAIRMVMFVANLPSTFARDVDLSPQMLGKE
>NZ_CP019636.1|WP_087539596.1|2752651_2753047_-|IS200/IS605-family-transposase
MKKFKSNNNVVYSCKYHVIFCPKSRRKVLVGAIASRLKELLAQVAIEIEVEILEMEIMPDHVHLLIEVDPQFGVHKAIKRFKGNSSRNLRLEFPELKTKLPILWINSYFVSTVGGAPLDVIKQYIQLQKEV
>NZ_CP019636.1|WP_157679395.1|2755340_2755484_-|hypothetical-protein
MVNGFPGIDKVTKNMGYKPRPSRATFDTIERLATQAESRAAAEEPVS
>NZ_CP019636.1|WP_087539598.1|2755491_2755791_-|hypothetical-protein
MKEFALSCEVVSREGDQLYSIEYAALITTVSTVLIQHLVELGLIEPIGTMLRSRDIARIAQIQRLHLDLGLNFVGAAMVLDMAQEIAQLKARIRAYQEQ
>NZ_CP019636.1|WP_087539600.1|2755787_2756783_-|J-domain-containing-protein
MATATDFKDYYAILGVDKNATPEDIKRAYRKLARKYHPDVNPGDKQAEERFKEINEAHEVLSDPEKRQKYDQFGQYWNQASQGGAPPPRRGAGVGTEGFDFDQYTNFDSFIDELLGGRFGTRGQTGRRTYTSRTYQPGTDEDVWSAFGGGTSPAADTEAAITLTFSEAFHGVQKRLQIDGETVNVRIPPGAKPGSRIRIKGKGRPSPFSQKRGDLYITIDVLPHPFFRFEGNNIACDLPIRPDEAVLGTQTKVPTPDGSVTMVVPRGVRSGQTLRLRGKGWIQPNNGRTDLLMKIQIVPPRDLSPLEQECYEKIQANTTFNPRSELEHVSL
>NZ_CP019636.1|WP_087539602.1|2756858_2757695_-|DUF2382-domain-containing-protein
MALVKLRDFYLDDREDNSDIDEIKNYDVYAGNDKVGSVYDLLVDEQTGRFRYFVVDTGFWIFGKKVLLPVGLANIDHSTRRINVNSLSRDQVENLPNYDDLERVDFDYEEQVRNAYRPMAASSGITQPTYDRNTYNYEQEPSLYNISDRDDQTLRLYEERLIANKERRKTGEVAIGKHIETETARVAVPLEKERVVIERTTPTDVTPVHPTDADFREGEVARMEIYEETPDIHKEAVVREEVRVKKVVEQDTAEATETIRREELDVDAPGLPIVDKQG
>NZ_CP019636.1|WP_087539604.1|2757982_2758558_-|hypothetical-protein
MSVNDKKLKQNFWKTLIYALVLNANFYENARNTPKTHQLALTIVIMAALSHALGSGVILLINRATLPVLFLGLLIDAFSIVIGYYFWTFTIWKIGQWLKPIDPTYGDLLSPIGFAYAPQVLNFLTVIPVLGRPIELILAVWSLLAVIVAVREGLDISTNRAAIICLLGWPLIQIAVGLLQVTEQQLIKYLT

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Crispr_ID: NZ_CP019636_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_7

3051164-3051256

Orphan

Consensus_repeat	Method
AGATTGCTTTCTCAATTAGTCTGCTTGCTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_7

>merge|NZ_CP019636|7|3051164-3051256|CRISPRCasFinder
AGATTGCTTTCTCAATTAGTCTGCTTGCTTCTTCATTTTGGTGTTTTCCGCAAGCGGACAAGCAGATTGCTTTCTCAATTAGTCTGTTTGCTT

>NZ_CP019636|7|7|3051164-3051256|CRISPRCasFinder
AGATTGCTTTCTCAATTAGTCTGCTTGCTT	CTTCATTTTGGTGTTTTCCGCAAGCGGACAAGC
AGATTGCTTTCTCAATTAGTCTGTTTGCTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087540082.1\|3062506_3063190_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP019636.1\|WP_087540077.1\|3059799_3061050_+\|S-layer-protein	unknown	unknown	gnl\|CDD\|306825
NZ_CP019636.1\|WP_087540068.1\|3051403_3051844_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239239
NZ_CP019636.1\|WP_087540054.1\|3043933_3044602_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP019636.1\|WP_087540059.1\|3046525_3047968_+\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|273776
NZ_CP019636.1\|WP_087546146.1\|3049253_3049931_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP019636.1\|WP_087540080.1\|3061652_3062504_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224054
NZ_CP019636.1\|WP_087540075.1\|3058481_3059162_+\|conjugal-transfer-protein-TrbI	unknown	unknown	unknown
NZ_CP019636.1\|WP_087540091.1\|3065661_3066168_+\|fatty-acid-hydroxylase	unknown	unknown	unknown
NZ_CP019636.1\|WP_087540057.1\|3044549_3045896_-\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP019636.1\|WP_087540050.1\|3041258_3041861_+\|heme-copper-oxidase-subunit-III	unknown	unknown	gnl\|CDD\|224758
NZ_CP019636.1\|WP_087540064.1\|3050493_3050784_-\|DUF1778-domain-containing-protein	unknown	unknown	gnl\|CDD\|226860
NZ_CP019636.1\|WP_087540088.1\|3064390_3065026_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087540070.1\|3053902_3054454_+\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|368559
NZ_CP019636.1\|WP_087540052.1\|3041973_3043548_+\|GMC-family-oxidoreductase	unknown	unknown	gnl\|CDD\|225186
NZ_CP019636.1\|WP_087540072.1\|3054509_3057536_-\|SMC-family-ATPase	unknown	unknown	gnl\|CDD\|223496
NZ_CP019636.1\|WP_087546145.1\|3047982_3049242_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|182528
NZ_CP019636.1\|WP_087540085.1\|3063448_3063775_+\|YbjQ-family-protein	unknown	unknown	gnl\|CDD\|376657
NZ_CP019636.1\|WP_157679433.1\|3043792_3043945_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087540062.1\|3049969_3050503_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379326

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087540082.1\|3062506_3063190_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	4.90736e-17
NZ_CP019636.1\|WP_087540068.1\|3051403_3051844_+\|hypothetical-protein	gnl\|CDD\|239239	cd02929, TMADH_HD_FMN, Trimethylamine dehydrogenase (TMADH) and histamine dehydrogenase (HD) FMN-binding domain. TMADH is an iron-sulfur flavoprotein that catalyzes the oxidative demethylation of trimethylamine to form dimethylamine and formaldehyde. The protein forms a symetrical dimer with each subunit containing one 4Fe-4S cluster and one FMN cofactor. It contains a unique flavin, in the form of a 6-S-cysteinyl FMN which is bent by ~25 degrees along the N5-N10 axis of the flavin isoalloxazine ring. This modification of the conformation of the flavin is thought to facilitate catalysis.The closely related histamine dehydrogenase catalyzes oxidative deamination of histamine.	0.00557695
NZ_CP019636.1\|WP_087540054.1\|3043933_3044602_-\|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].	1.21771e-73
NZ_CP019636.1\|WP_087540059.1\|3046525_3047968_+\|efflux-RND-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|273776	TIGR01730, COG0845:_Membrane-fusion_protein, RND family efflux transporter, MFP subunit. This model represents the MFP (membrane fusion protein) component of the RND family of transporters. RND refers to Resistance, Nodulation, and cell Division. It is, in part, a subfamily of pfam00529 (Pfam release 7.5) but hits substantial numbers of proteins missed by that model. The related HlyD secretion protein, for which pfam00529 is named, is outside the scope of this model. Attributed functions imply outward transport. These functions include nodulation, acriflavin resistance, heavy metal efflux, and multidrug resistance proteins. Most members of this family are found in Gram-negative bacteria. The proposed function of MFP proteins is to bring the inner and outer membranes together and enable transport to the outside of the outer membrane. Note, however, that a few members of this family are found in Gram-positive bacteria, where there is no outer membrane. [Transport and binding proteins, Unknown substrate].	1.07488e-45
NZ_CP019636.1\|WP_087546146.1\|3049253_3049931_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	8.36965e-120
NZ_CP019636.1\|WP_087540080.1\|3061652_3062504_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	5.24297e-112
NZ_CP019636.1\|WP_087540057.1\|3044549_3045896_-\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	3.07832e-58
NZ_CP019636.1\|WP_087540050.1\|3041258_3041861_+\|heme-copper-oxidase-subunit-III	gnl\|CDD\|224758	COG1845, CyoC, Heme/copper-type cytochrome/quinol oxidase, subunit 3 [Energy production and conversion].	1.23016e-61
NZ_CP019636.1\|WP_087540064.1\|3050493_3050784_-\|DUF1778-domain-containing-protein	gnl\|CDD\|226860	COG4453, COG4453, Uncharacterized protein conserved in bacteria [Function unknown].	4.8093e-27
NZ_CP019636.1\|WP_087540070.1\|3053902_3054454_+\|Uma2-family-endonuclease	gnl\|CDD\|368559	pfam05685, Uma2, Putative restriction endonuclease. This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. A small number of member proteins also contain pfam02861 domains that are involved in protein interactions. Solutions of several structures for members of this family show that it is likely to be acting as an endonuclease.	9.27423e-31
NZ_CP019636.1\|WP_087540052.1\|3041973_3043548_+\|GMC-family-oxidoreductase	gnl\|CDD\|225186	COG2303, BetA, Choline dehydrogenase and related flavoproteins [Amino acid transport and metabolism].	8.4048e-72
NZ_CP019636.1\|WP_087540072.1\|3054509_3057536_-\|SMC-family-ATPase	gnl\|CDD\|223496	COG0419, SbcC, ATPase involved in DNA repair [DNA replication, recombination, and repair].	3.90603e-119
NZ_CP019636.1\|WP_087546145.1\|3047982_3049242_+\|FtsX-like-permease-family-protein	gnl\|CDD\|182528	PRK10535, PRK10535, macrolide ABC transporter ATP-binding protein/permease MacB.	1.73157e-68
NZ_CP019636.1\|WP_087540085.1\|3063448_3063775_+\|YbjQ-family-protein	gnl\|CDD\|376657	pfam01906, YbjQ_1, Putative heavy-metal-binding. From comparative structural analysis, this family is likely to be a heavy-metal binding domain. The domain oligomerizes as a pentamer. The domain is about 100 amino acids long and is found in prokaryotes.	5.89337e-37
NZ_CP019636.1\|WP_087540077.1\|3059799_3061050_+\|S-layer-protein	gnl\|CDD\|306825	pfam00395, SLH, S-layer homology domain.	4.64509e-12
NZ_CP019636.1\|WP_087540062.1\|3049969_3050503_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379326	pfam13673, Acetyltransf_10, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	5.99426e-09

>NZ_CP019636.1|WP_087540064.1|3050493_3050784_-|DUF1778-domain-containing-protein
MQIEPTPVNRNRDVTINIRAHQTQRDLIDRAAEALGKSRSDFMLETACREAEAVLLDRRLFILDDEKFQQFMDLLDAPPTENENLRKLLTTKAPWD
>NZ_CP019636.1|WP_087540062.1|3049969_3050503_-|GNAT-family-N-acetyltransferase
MGLEVVKEENQKLQSPQPINPHHLLEDFDSGNADLNDWLRRRAVKNEDSGASRTYVVTVGQKVIAYYCLATGSVLSSIAPGRVRRNMPDPIPVMVIGRLAVDRNWHSQGIGRGLVRDAVLRKVQAAQIAGIRAILVHAISEEAKKFYEKCGFISSPVSPMTLLVTVADAKAALSIFE
>NZ_CP019636.1|WP_087546146.1|3049253_3049931_+|ABC-transporter-ATP-binding-protein
MIWMEDITKTYRLGDAEVPILKGIDLAIEEGEYVAIMGMSGSGKSTLMNIIGCLDRPTSGHYVLEGRNLTTLNNDELAYIRNQRLGFVFQQFNLLPRATAVENVMLPMVYAGVPRDKRRKRAIEALTRVGLAERLHNRPNQLSGGQQQRVAIARALVNRPALVLADEPTGALDSQTSQEVMDLLTDLNNQGITIVIVTHEADIAAQTQRVIHVRDGLIVSPVNSR
>NZ_CP019636.1|WP_087546145.1|3047982_3049242_+|FtsX-like-permease-family-protein
MVKSIRPTKVSLFEILSMAVEAMWSNRLRTGLTMLGVIIGISSVIAVTSVGQGVQKATEQQIQALGSNVLLVLAGAARSGGISQGFGSASTLTWEDAQAVSQQVPAAQSVTAYLQRAVQVVYAGQNISTQVLGTDLNYPDVKNIHPQEGQYFTQEDLNNATPVVVLGSKVRDDLFGVGSSAIGADIRIQNGRYKVIGVMESKGAAGAQNVDDQMYIPLTNMSARIVGNNALNGTAINGLWLKAQDEAQLDAAQFQVTNLLRIRHNIYPPQPDDFRIINQVDIINTFSSVVGLFTILVGAIAGISLVVGGIGIANIMLVSVVERTREIGIRKAVGATYSAILSQFLTEAVAVAIVGGMIGIGFGICLALIAANLFKFPFVVSFWSIIAGFGFSLLTGLVAGVIPARNAAKLDPITALRSD
>NZ_CP019636.1|WP_087540059.1|3046525_3047968_+|efflux-RND-transporter-periplasmic-adaptor-subunit
MAKVEEVSDLAKSSQSWKQASPVKDLKQIKIPKWLVGLLILGLLGGGGYLGVRQFMMVQRQERQSRIQTAVVEKTNLPVTISANGNVQPERSINVSPKTSGVLKKLLVKEGDRVQQGQILAYMDDSNLRGQLTQANGQLENAQANLRLLLAGSRSEDIAKAQADVRNNQAQLVQAQSRLDLASLRVKRLSTPTQEGAVSRDTLDEALTEERNAKDNLEQVKASLAAANQELAKLNNGSRPEEIEQARAQVVSAQGSLQTIQAQINDTVIRAPFTGLVTRKFADPGAFVTPTTAGSEVSSATSSSILALASQNQVTAKVAETNISQIKVGQTVTIQADAYPDKKFTGKVVQVAAQSTVEQNVTNFEVKSSLSDPENILRAGMNVNVDFNVGKLDNALVIPTVAIVRQENASGVMVLTPGNNRRPRFRPITTGVTVGNKTVVRSGLQEGERVMLSFPAGQRPQGSGTSRGMTPFGGPPTRFR
>NZ_CP019636.1|WP_087540057.1|3044549_3045896_-|sensor-histidine-kinase
MSRSLPSLRLLLYLEWLLLGMSLLTGFLVPPIYPFQGSPWLTVLSIVAFGVMGLRLPTQKFTYKVLYTAVELGIVLLPAFTNSHLCFGPLLGLIAVIRSCQMFNLQGRLIVASLVYVSYLYMVFLRSRTTVFFKMHIGQGKPVAEQIATNTANLILNNAISFALTLTFVLLLVNAVLSERRSRQELAIAHEQLRQYALRIENQATLQERNRIAREIHDSLGHTLTAQTIQLENALLLLPSNIDQSIDIDKSIDKAIEFLKEAKQLAYQALQEVSRSVATLRADPLRGKSLENAIHNLIRDFSSATTFTPDCKISLIYPVTPEVGIAVYRILQEALTNISKHSAATQVSVQLQSLAGKLHLLIVDNGRGFYPEQNTTGFGLQGMRERAIALGGKFQIISEPAKGCRIQVNIPIIDSSVVNSESAMNIKNSKLYDSSVADRRPNHYSSGT
>NZ_CP019636.1|WP_087540054.1|3043933_3044602_-|response-regulator-transcription-factor
MIRLLLIDDQIIIRQGLKTLLESKSDLQVVGDAENGQLAIEAVEALYRTPLQPDVVLMDVRMPVMDGVAATRLICQRFPEIHVLVLTTFDDDEYVSQAMRYGARGYLLKHTPLDELAIAIRAVHQGYTHMGPGLFEKALNTPDISDSLQPAIPLELAQLSPREKEVLRLIAMGLSNREIAHMLYISERTVRNHVTSILSQLQLRDRTQAALLARTFLPQLEI
>NZ_CP019636.1|WP_157679433.1|3043792_3043945_+|hypothetical-protein
MRYGLRPNTSYKSFIAFMQAVWLRQMVCAAMRKALAVRFTEAKSTGVSNF
>NZ_CP019636.1|WP_087540052.1|3041973_3043548_+|GMC-family-oxidoreductase
MIIDDQHYDLIIVGTGAGGGTLLHKLAPTGKKILVLEKGNFLPRENENWNASEVFGKGRYHAREQWYDISGEPFRPQTNYWVGGNTKFYGAALLRMREKDFEKVQHQDGISPEWPLQYQDFEPYYTQAEKLYSVHGRQGDDPTEPPRSEDYPYPPISHEPRMQQICEALSHHGLHPGYLPLALRLNENNIDESLCIRCKTCDGFPCQVDGKADAEVSGVIPALEFPNVTLKTDANVVRLHTSTSGREVKAVEVEIGGQSYLFFGDIVVLACGAVNSAALLLRSANEKHPTGLANSSDQVGRNFMKHLLTAVVQLSSIPNPAVFQKTIYVHDFYWGDSDFEYPMGHIQNTGNILQDMIPAEAPPLLSLLSRLMPGFGLQQLATRTIGWWLQTEDLPDPNNRVRVQGSKLYLDYTPNNVEAHDRLIYHWTEVLKAVDRTGKNSMLSMGVYPHSNTPIRVVAHQSGTCRFGEDPTTSVLDLNCRTHDVNNLYIVDGSFFPSSAAVSPALTIIANALRVGEHLIEQLN
>NZ_CP019636.1|WP_087540050.1|3041258_3041861_+|heme-copper-oxidase-subunit-III
MDSSIKAEQLQQPLHEHAHDEEGNKMFGFVVFLLSESVIFLSFFAGYIVYKTTTPDWLPPGVSGLEIKEPAINTVVLVASSFVIYLAERALGRHELNKFRLFLLTTIAMGTYFLVGQAIEWSNLAFGFTTGVFGGMFYLLTGFHGLHVLTGIILQLIIFARSFIPGNYDSSHFGVNATSLFWHFVDVIWIILFVLIYIWQ
>NZ_CP019636.1|WP_087540068.1|3051403_3051844_+|hypothetical-protein
MARRKRTSQVLEKAVRRAAGINSIAANLDLGNGLSVPAFSRLIETMRTRQDAYNSALSNLDKLYREMLETERELGDMAEHMLLGVATRYGKSSVEYGMAGGVPKNQRRKRLRGDSLTASSEQPSFIASVEVNENGNKAVATSQDVR
>NZ_CP019636.1|WP_087540070.1|3053902_3054454_+|Uma2-family-endonuclease
MTIIAAKWTIDEYHRMIDAGILSDRQVELLKGEIVEMSPEGEPHAYSSHEAGEYLTQLLVKYATIRQAKPITLPNDSEPEPDIAIVQRLGREYREHHPYPENIFWLIEYANSSLEKDLETKSKIYAEVGIPEYWVVNLKKLHLVVFREPLDGEYATKLTLTGGTIQPLAFPDVSVSVEQIINS
>NZ_CP019636.1|WP_087540072.1|3054509_3057536_-|SMC-family-ATPase
MIPIQLILKNFLSYRDTTLDFRGLHTACICGSNGAGKSSLLEAITWAIWGQSRASSEDDVIHTGAKEVRVDFIFEANQQTYKVIRTRVRGGSGALEFQIQTPTGFRALTGKGVRATQDLILEHIKLDYDTFINSAYLRQGRADEFMLKRPGERKEILAELLKLNQYDELEERAKELSRQFKARTEELERCLDSLKSQLQQREATAQKQAELEAQINELQQVQAFENIQLQSLQVVQHQRQNWEQQLNFIRQQYQNLTQDCDRLQQEHSVIDSQLSDLEELLAQEAEIKAGHDEYQTLQSQEETMGAKFEEYTRAQQARQQKQQQLTKQINELERQLQHAEAQLGALQQQEQELQQTLSKSDEVEAALAQLAAARNRLTQMDQLQLQVAPLLQQRVTLQSQLDRAQAGLVARLEQLEATQNQLQRQHRRQPQLQQAVMEVAMQIEELEKKRVYLQRVQEKGQERRHLIERLQAHQRDFEKLLAELQQKLQMLQNPNAICPLCERPLDEHHWNRVVDKTKVEYKDAEDELWIVRERMAVSDREIQVLRQEYREISQQLSPYDTLREQRGQLAAQLQATSDVEQQLQQIVVEKQHLERSLEVGDYAHNIHTELQHLGQYLQQLNYNEQDHALARNEVERWRWAEIRLSQIKDAAKRQAQIEVRKPELQAQIAQLHTRIKQEATESECARQIAALDRHITEIGYISEQHNNFRMAVRKAQAWQLRYQQLVGAQQQYPQLKTRLQELEVSLQARLTERQRLAVQIESIVQQLEESANPSAQIQVLEQQLLSRRRQLDEQIAQLGRLQQLAHQLETLQLEYEQQQQQLQQVKRQHRIYQELSQAFGKNGIQALMIENVLPQLEVETNQLLSRLSGNQLHVQFVTQRAGKSGKATKKNAKLIDTLDILIADARGTRAYETYSGGEAFRINFAIRLALAKLLAQRAGAALQLLIVDEGFGTQDAEGCDRLIAAINAIASDFACILTVTHMPHLKEAFQARIEVNKTQQGSQVRLMV
>NZ_CP019636.1|WP_087540075.1|3058481_3059162_+|conjugal-transfer-protein-TrbI
MTQFHRWKSGAVALIAMAMTTGTIAPMFLLTPASAQTIFRGQQTQTGTVSIPAGVTLPVTYEKDKIVVTPDETAPIKLKIARNIVDSSRRVLIPEGSEIVGQLQPITRNGEKGTYFVAQEIVFPKGERQSINATSQVITRKETISKGAKTGTILQDAAIGAGAASVISLITGNRRIEALEPILGAGAGAAASVLLRRNKAEVIVVEPQRGELDLTLRSSFQVSRGY
>NZ_CP019636.1|WP_087540077.1|3059799_3061050_+|S-layer-protein
MFGDFRWQSGCAAFITLGITAGTIAPLVTPTASFAQTNFTDVQSNYWATEFIQQLAQRGVIAGFPDGSFRPEEPVTRAQFAAMIGKAFQKAPERQAVRFYDVPNGYWASSAIQDAYTTGFLSGYPGNRFEPNQNIPREQVLVSLANGLVYNVSGNTESILQYYNDANNISGYARSPIAAASEKQIVVNYPNIKFLNPKATATRAQVAAFIYQALVSSGKAAAINSPYIVAFGQPTPSQPVAVTIPEGTVIPIRYEKAEKILVTKDETAPLTLTVAQNVVTDRGNVVIPAGSQVVGELRPVKSKGGSQFVAQKLVLANGQQYPINATSEVITKTETIKQGTSTRAIAKNAALGAGAAAAVSAVIGDRAIATEEVLGGAAIGGLIGVFFGKKSVDLIAIDPNTDLQMTIGENFQISLK
>NZ_CP019636.1|WP_087540080.1|3061652_3062504_+|ABC-transporter-ATP-binding-protein
MTVAVQLENVYKIYNNVPVVNDLSFTIKAGEMFGLLGPNGAGKSTTIRMLTTLTQPTQGQIEVSGYNVVRQPIRAKQCIGVVLQQVSVDGDLTVWENMELHGRLHHIANPQRQRLINQWLEYVELVTRRNDLVKTLSGGMKRRLQIARALLHQPQILFLDEPTVGLDPQTRRRLWEIIRDLNKQGMTILLTTHYMDEVEYLCHRIGIMDGGKLISLGTLQQLRSAHGEGLVMKQIGDRWEYLFFPTVEDANLYLNQQEDKTGMMVRPSNLEDIFVELTGRKLD
>NZ_CP019636.1|WP_087540082.1|3062506_3063190_-|tetratricopeptide-repeat-protein
MYNRTSFILSILLVGSFVATIPLVAQAQEAVPQQQSSQELKELLEEGRRLVDSGDYNGAIAVYQRATTLEPKNATIYSGIGYLYAQQGNFPAALQAYRRAVALNPNNSDYQYALGYVSGNLGDNKGAKEAYRRAIQANRNNVNAYIGLATVLLRLGENENVKWAYEQAVNLDPKNPQVIELRGNILVKQGKSKEAIAVFQKARDLYEKQGRQDSVARVEAVLRTLGG
>NZ_CP019636.1|WP_087540085.1|3063448_3063775_+|YbjQ-family-protein
MILTTTDVIQGAIIQSYLGIVTAEVVYGSNFLRDFFASIRDIIGGRTGSYERLFEEGQRKALEELERRALRLGADAVIGIEVDTGTINVDQSGVLILITATGTAVKLR
>NZ_CP019636.1|WP_087540088.1|3064390_3065026_+|hypothetical-protein
MSYTNRVGDEVINEPAVVGRVSDYHDRVRWGPIIAGLLIALATQLILSSIFAAIGAGSIEASGRPRTIAPNVAQNVGIWSTIALLIALFTGSWVMARACGPMNRNTALLNGAILWATTLAVSSWLLASGVSGAFGIAASNAGQVINQVQQPGGGVNVPQNLPNVTAEEARRIAANVRSGLWWFVFGSLLGLVASLLGAATGTRSPRTNHYA
>NZ_CP019636.1|WP_087540091.1|3065661_3066168_+|fatty-acid-hydroxylase
MLKAIACAWILLIVGDFLSTFCYHIPEHVFGILHLRTHHSYKKNFRHYAILTFNLQVLLDGILGALPYLLMGVVLWYFSPIGVLCGLLIGQFHVWWRHTSILGWQTPKPVDFLCRILFVTTPERHWQHHQKTNQGFGDIFTFFEPPAKSWLRLLRLLRLRFTHRLVSQ

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Crispr_ID: NZ_CP019636_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_8

3283752-3283832

Orphan

Consensus_repeat	Method
ATGCGTTTGAGGTTAGCTTTTGCTTCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_8

>merge|NZ_CP019636|8|3283752-3283832|CRISPRCasFinder
ATGCGTTTGAGGTTAGCTTTTGCTTCTGCTATTTCTTGGTCTTTGGATGCTTGAATGCGTTTGAGGTTGGCTTTTGCTTCT

>NZ_CP019636|8|8|3283752-3283832|CRISPRCasFinder
ATGCGTTTGAGGTTAGCTTTTGCTTCT	GCTATTTCTTGGTCTTTGGATGCTTGA
ATGCGTTTGAGGTTGGCTTTTGCTTCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087540445.1\|3273248_3275942_-\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|225837
NZ_CP019636.1\|WP_087540447.1\|3276346_3277006_-\|OmpA-family-protein	unknown	unknown	gnl\|CDD\|143586
NZ_CP019636.1\|WP_087540442.1\|3272774_3273242_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP019636.1\|WP_087546165.1\|3278505_3279168_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP019636.1\|WP_087540473.1\|3289924_3290986_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|223506
NZ_CP019636.1\|WP_087540477.1\|3292545_3293598_-\|UDP-3-O-(3-hydroxymyristoyl)glucosamine-N-acyltransferase	unknown	unknown	gnl\|CDD\|234858
NZ_CP019636.1\|WP_087540479.1\|3293797_3295150_-\|murein-transglycosylase-A	unknown	unknown	gnl\|CDD\|225377
NZ_CP019636.1\|WP_087540465.1\|3285807_3286386_-\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|368559
NZ_CP019636.1\|WP_087540454.1\|3279169_3280399_-\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP019636.1\|WP_157679443.1\|3292231_3292483_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546166.1\|3282038_3283220_-\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|130253
NZ_CP019636.1\|WP_087540467.1\|3287043_3287457_-\|putative-toxin-antitoxin-system-toxin-component,-PIN-family	unknown	unknown	gnl\|CDD\|224485
NZ_CP019636.1\|WP_087540475.1\|3291143_3291887_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP019636.1\|WP_087540458.1\|3281314_3282010_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|274374
NZ_CP019636.1\|WP_087540456.1\|3280748_3281210_+\|P-pilus-assembly/Cpx-signaling-pathway,-periplasmic-inhibitor/zinc-resistance-associated-protein	unknown	unknown	gnl\|CDD\|226203
NZ_CP019636.1\|WP_087540450.1\|3277139_3277922_-\|ion-transporter	unknown	unknown	gnl\|CDD\|366146
NZ_CP019636.1\|WP_087540471.1\|3288223_3289774_-\|pentapeptide-repeat-containing-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP019636.1\|WP_087540469.1\|3287446_3287722_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087540463.1\|3285026_3285647_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP019636.1\|WP_087540452.1\|3278069_3278495_+\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|223663

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087540445.1\|3273248_3275942_-\|PAS-domain-containing-protein	gnl\|CDD\|225837	COG3300, COG3300, MHYT domain (predicted integral membrane sensor domain) [Signal transduction mechanisms].	3.69961e-77
NZ_CP019636.1\|WP_087540447.1\|3276346_3277006_-\|OmpA-family-protein	gnl\|CDD\|143586	cd07185, OmpA_C-like, Peptidoglycan binding domains similar to the C-terminal domain of outer-membrane protein OmpA. OmpA-like domains (named after the C-terminal domain of Escherichia coli OmpA protein) have been shown to non-covalently associate with peptidoglycan, a network of glycan chains composed of disaccharides, which are crosslinked via short peptide bridges. Well-studied members of this family include the Escherichia coli outer membrane protein OmpA, the Escherichia coli lipoprotein PAL, Neisseria meningitdis RmpM, which interact with the outer membrane, as well as the Escherichia coli motor protein MotB, and the Vibrio flagellar motor proteins PomB and MotY, which interact with the inner membrane.	2.19204e-31
NZ_CP019636.1\|WP_087540442.1\|3272774_3273242_+\|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.	3.55058e-16
NZ_CP019636.1\|WP_087546165.1\|3278505_3279168_-\|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].	1.29362e-86
NZ_CP019636.1\|WP_087540473.1\|3289924_3290986_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|223506	COG0429, COG0429, Predicted hydrolase of the alpha/beta-hydrolase fold [General function prediction only].	1.43496e-101
NZ_CP019636.1\|WP_087540477.1\|3292545_3293598_-\|UDP-3-O-(3-hydroxymyristoyl)glucosamine-N-acyltransferase	gnl\|CDD\|234858	PRK00892, lpxD, UDP-3-O-[3-hydroxymyristoyl] glucosamine N-acyltransferase; Provisional.	7.05952e-153
NZ_CP019636.1\|WP_087540479.1\|3293797_3295150_-\|murein-transglycosylase-A	gnl\|CDD\|225377	COG2821, MltA, Membrane-bound lytic murein transglycosylase [Cell envelope biogenesis, outer membrane].	1.87458e-136
NZ_CP019636.1\|WP_087540465.1\|3285807_3286386_-\|Uma2-family-endonuclease	gnl\|CDD\|368559	pfam05685, Uma2, Putative restriction endonuclease. This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. A small number of member proteins also contain pfam02861 domains that are involved in protein interactions. Solutions of several structures for members of this family show that it is likely to be acting as an endonuclease.	6.48225e-48
NZ_CP019636.1\|WP_087540454.1\|3279169_3280399_-\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	2.48429e-59
NZ_CP019636.1\|WP_087546166.1\|3282038_3283220_-\|FtsX-like-permease-family-protein	gnl\|CDD\|130253	TIGR01185, membrane_spanning_subunit, DevC protein. This model describes a predicted membrane subunit, DevC, of an ABC transporter known so far from two species of cyanobacteria. Some experimental data from mutational analysis suggest that this protein along with DevA and DevB encoded in the same operon may be involved in the transport/export of glycolipids. [Transport and binding proteins, Other].	9.97877e-157
NZ_CP019636.1\|WP_087540467.1\|3287043_3287457_-\|putative-toxin-antitoxin-system-toxin-component,-PIN-family	gnl\|CDD\|224485	COG1569, COG1569, Predicted nucleic acid-binding protein, contains PIN domain [General function prediction only].	3.13968e-35
NZ_CP019636.1\|WP_087540475.1\|3291143_3291887_+\|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].	2.34478e-90
NZ_CP019636.1\|WP_087540458.1\|3281314_3282010_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|274374	TIGR02982, heterocyst_DevA, ABC exporter ATP-binding subunit, DevA family. Members of this protein family are found mostly in the Cyanobacteria, but also in the Planctomycetes. Cyanobacterial examples are involved in heterocyst formation, by which some fraction of members of the colony undergo a developmental change and become capable of nitrogen fixation. The DevBCA proteins are thought export of either heterocyst-specific glycolipids or an enzyme essential for formation of the laminated layer found in heterocysts.	1.45095e-144
NZ_CP019636.1\|WP_087540456.1\|3280748_3281210_+\|P-pilus-assembly/Cpx-signaling-pathway,-periplasmic-inhibitor/zinc-resistance-associated-protein	gnl\|CDD\|226203	COG3678, CpxP, P pilus assembly/Cpx signaling pathway, periplasmic inhibitor/zinc-resistance associated protein [Intracellular trafficking and secretion / Cell motility and secretio / Signal transduction mechanisms / Inorganic ion transport and metabolism].	5.59145e-11
NZ_CP019636.1\|WP_087540450.1\|3277139_3277922_-\|ion-transporter	gnl\|CDD\|366146	pfam00520, Ion_trans, Ion transport protein. This family contains sodium, potassium and calcium ion channels. This family is 6 transmembrane helices in which the last two helices flank a loop which determines ion selectivity. In some sub-families (e.g. Na channels) the domain is repeated four times, whereas in others (e.g. K channels) the protein forms as a tetramer in the membrane.	1.6592e-17
NZ_CP019636.1\|WP_087540471.1\|3288223_3289774_-\|pentapeptide-repeat-containing-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	9.21765e-27
NZ_CP019636.1\|WP_087540463.1\|3285026_3285647_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	3.61987e-13
NZ_CP019636.1\|WP_087540452.1\|3278069_3278495_+\|nucleoside-deaminase	gnl\|CDD\|223663	COG0590, CumB, Cytosine/adenosine deaminases [Nucleotide transport and metabolism / Translation, ribosomal structure and biogenesis].	3.91435e-48

>NZ_CP019636.1|WP_087546166.1|3282038_3283220_-|FtsX-like-permease-family-protein
MIQEIQQLQRRTPLGWLQLSHQKGRLLVALAGIAFADVLMFMQLGFQTALFDTNTRLHRSMDADIFLMSPQGRNIAYLSKIPRRRLYQAMDIPGVKSAEGMYLGFIDWKNPQTRKETGVLVIGFNPDQPAFDIPEVNRQLNILKLPDTVLFDRGTRGDYAEAIAQVEQGKAVTTEIERRTITIGGLFQMGASFVADGSLITSDQNFLRLFPRQQSTSVNLGLIKLQPGYEPQQVANSLKSYLGNSQDVKVLTKEEFVEFEKNYWQTNTAIGFIFSLGVSMGFMVGVIIVYQVLSTDVNAHMKEYATFKAMGYRNAYLLSVVFEEAIILAVLGFLPGVTVSFGLYTLTRNATNLPVYMTIARVIQVQVLTIIMCMISGAIATRKVQSADPADMF
>NZ_CP019636.1|WP_087540458.1|3281314_3282010_-|ATP-binding-cassette-domain-containing-protein
MNQPVISIQNLNHYFGKGQLRKQVLFEINLEINAGEIVIMTGPSGSGKTTLLTLVGGLRSAQEGSLRVLGRELCGASAHQLTLTRRSNGYIFQAHNLHGSLTALQNVRMGLELHKGMTPQQMQRQSAEMLELVGLGNRLNYYPDDLSGGQKQRVAIARALVSHPKIVLADEPTAALDSKSGRDVVNLMHNLAKEQACTILLVTHDNRILDIADRIVYMEDGKLAKAPAAVG
>NZ_CP019636.1|WP_087540456.1|3280748_3281210_+|P-pilus-assembly/Cpx-signaling-pathway,-periplasmic-inhibitor/zinc-resistance-associated-protein
MKLKKLSLIFGAIALSLTVTSFAIKAEANSTSPIVVAQSWEKGGREKEGPLQRLGLTDEQKTKMKEIRRNTRAEVEKILTEQQREQLQTAMQNRQGRRSAFSSLNLSDEQKSQLQQVMQSQKTQMDAVLTAEQKAQLQKYREEMRSRRPQRNM
>NZ_CP019636.1|WP_087540454.1|3279169_3280399_-|sensor-histidine-kinase
MSRPIYFNNHPFRFLLYLEWILLAFAAFTAVLPSHPDRPHMRFPELTICSLMFFGFMGLRLPTRNYITKIIYTSIEIFLISITGFLGGKTARLFPFLYIILVTRSCLIFQLPGRIVVTVLSFIFFLLTLRRRFERMPLSPATQERFWFFTLSFVLVFGLSLVFVLLLMNAVLSERQSREKLAIANEKLRQYALRIENQATLEERNRIAREIHDSLGHSLTALNLQLETALKLWQSHPTKAQTFLAKAKELGSKALQDVRQSVSTMRSHPLQEQSLEQAIAGLAENVQRSTGVAPICQIHLSHSIPVEMSTAIYRIVQESFTNICKYAQATVVKLEITTTKTSLELKIEDNGLGFDLTQNTTGFGLQSMRDRTLALDGHFHIYSTPGSGCKITATIPLSLSLLTVREIHD
>NZ_CP019636.1|WP_087546165.1|3278505_3279168_-|response-regulator-transcription-factor
MIKVLLVDDQNLIRQGLKALLELEPDLEIVGEAENGEIGLHFIEQLYPDVVLMDIRMPVMDGVATTREIQKRFPKIKVLVLTTFDDDEYVKAALQNGAMGYLLKDTPSEELAVAIRAVHKGYTQLGPGIVKKLLNQFSHVTPTQSPSPPPSLAELTPREKEVLQLIAIGASNREIAQQLYISEGTVKNHVTNILNRLNLRDRTQAAIFANSFFPSLNDPN
>NZ_CP019636.1|WP_087540452.1|3278069_3278495_+|nucleoside-deaminase
MNPEDFMRLALEEARKGDAPYGAVIVKDNEVVALAHNTVRRDSDPSAHAEINVIRSLTTKLKNPSLEGYTIYTTGEPCPMCASACIWTGLSEIIYGASIEDLVSLHQSQIHISCDEVIAKSSRKIKVRKGLLREECLQLFQ
>NZ_CP019636.1|WP_087540450.1|3277139_3277922_-|ion-transporter
MLFFREKTAFYLKDLETPVGKFVNLTIAGLVLLSSGIFVAETYNIPDILRFYLDTIDTVILLIFAAEYLLRFWSEENKIKYIFSFYSIIDLMAILPFFLGTVDISFIRILRWFRILRLIRFIDKKILFGRSTEDSLIPVRILFTLFAIIFVYSGLIYQVEHPVNPEVFVTFLDAFYFSIVTMTTVGFGDVTPISELGRLLTVLMILTGIALIPWQVGDLIKRLVKNANQVETVCSGCGLSFHDADAKFCKTCGMKLRKTL
>NZ_CP019636.1|WP_087540447.1|3276346_3277006_-|OmpA-family-protein
MYLLRFSIYLVPIALTIVASNFIHHTIAKARTNIQKLQLSAVKFSEVKKPAANLSQVRRIPSVKFPKNTYPAVKLPDIKSPQIQIQENKYLTIITLPTDLLFDHHDKDMIRPDAENMLRQVSQTINKYYPDTWLQILGHTDSQGSQNDNLKLSEQRVAAVQRWLSEKGGIAISLMSKEGYGEAQPIAPNQKSDCSDNPLGQQKNRRIEIVIQKLVNNQV
>NZ_CP019636.1|WP_087540445.1|3273248_3275942_-|PAS-domain-containing-protein
MLQADVGMISTYDPLLVVLSIVIAVFASYTALDLTGRVTVSQGWARRAWLIGGAIVMGIGIWSMHFVAMLAFSLPIPMGYDVLTVILSVLPAIVASGGALFLTSRPILNVQQLLIGGVLMGIGVASMHYIGMVAMQMEATTHYDPALFVASVAIAIVASVVALSIAFQLRLQMGRTGRRRKLSSAFIMAIAISGMHYTGMAAASFTPTRVAGIAITKTMQGSLSALAVGIGVATLIILGFTLLTSFVDRRMVTQAVLLKQQEAIRSQLFTDITLRIRRSLKLEDVLDTTVSEVRQALNMDRVIIYRFNPDKSGTIIAESVADGWIKILGRTVHDPLHQDAIDIYKNGQVRATHNIYDTDFTDFHRQILEGFQIKANLVAPVLNNNQLLGLLCGHQCSGLRIWQKSEISLFGQLAIQVSIALEQANLLYELQQAQEVLRLRDRAVAAASNGIVISDPRQPDDPIVFCNPAFEKMTGYSQKEVLGRNCRFLQGPDTDPATIEQIRSALRQEQECHVVIKNYRKDGTPFWCELSISPVKDMTGQVLNFVGIQSDITLRRQVEEELRRSKEVLQRQLVELIGDIKEVATGDLTARANITTGQIGIVADFFNTIIESLRQIVIQVKQAAQQVNVSVGENSDAIRQLADEALQQAEEITCTLDSVNRMNLSIQEVANSAHQAAEVARTSANTALDAGEAMERTVTSIFMLRETITETAEKIKRFGESSQEISKVVTLINEIALQTNLLSINASLEASRAGEESQGFMIVAQEVGRLAAQSAQATQEIEHIAKNIQSETEAVVQAIEQGTTQVLEGAHLVKDVKQSMEKIVEVSRQIDELVQSISQTTVSQAQTSQAVALFMQEVAKTSERTADSSRVVSTSLQQTVEVAQQLQASVSVFKTGE
>NZ_CP019636.1|WP_087540442.1|3272774_3273242_+|GNAT-family-N-acetyltransferase
MSQFQIREDDLTGKKIADLLREHLENMYEITPPESVHALDLEALRSPDITFWTAWEGDELLGCGALKELDSRSGEIKSMRTAKAHRRRGVASKILEHIIQEAKRRGYDCLNLETGAFPEFAPARALYTRYGFEYRGPFAEYIDDPNSVFMTKKLA
>NZ_CP019636.1|WP_087540463.1|3285026_3285647_+|TetR/AcrR-family-transcriptional-regulator
MVREKVTEVEADSSLDKVEQILQGAMHEFLLHGYAGTSMDRVATSAGVSKATVYSHFQDKQGLFKALIEKLAQERFHSIFGTEHLEGDPKIVLRRLATKALNQMLKDEEFHAFKRVLIGESGRFPELAQFCILCLIKPTIETLSHYLASHPELEIPDSEATARILLGSLVHFVMTQEMMNGQEIIPMESDRLIDALMHLILKSDRS
>NZ_CP019636.1|WP_087540465.1|3285807_3286386_-|Uma2-family-endonuclease
MSALILQLPPSLKLTDEEFEQLVAVNQELRLELDAQGELIIMSPTGGETGNRNFNLLGQLWFWSRQNNFGKAFDSSTGFKLPNGATRSPDASWITIERWERLTPQQRKKFLPLCPDFAVELVSESDEIEETQAKMREYIENGLRLGWLIHPQEKQVEIYRPHVAVEVLNFPKSLSGEDVLPGFVLDLEAIFS
>NZ_CP019636.1|WP_087540467.1|3287043_3287457_-|putative-toxin-antitoxin-system-toxin-component,-PIN-family
MTNKQRFVFDTNVLISAFLFSQSKPRQALDQAQDIGVLIFSSSVFSELKEVLYRPKFDRYLTGERRQELLEDLTQTAQFIDVIEQISECRDPKDNKYLELAVSGQAECIVTGDDDLLVLNSFRGIEILTVQKFLAKN
>NZ_CP019636.1|WP_087540469.1|3287446_3287722_-|hypothetical-protein
MRNYGSKQTMITKEEITIKVPSEVAEAYRNASEEEREQLQLKIAAIMQSQFTTDRQQAITRLRNTMDKASLEAQERGLTPEILESILNDDE
>NZ_CP019636.1|WP_087540471.1|3288223_3289774_-|pentapeptide-repeat-containing-protein
MDLSNPGPIISAVAAPIIKDKLQRSEVVIELLKRFKLSPDHPPSNFSGVYAYALVEYGVGKPKPFLELFRHNKIKQAFRKAFDDSNSLILQSEVDKFVDAYALGDEIKTLGLDIKREVAAFTAVFIEVVNRSRTPADTMMQHQIVSLHRKVETITEQVERLGSVDISRVYLYAVKRKMEADIKAERTFTSLADKLYFLCELSWEMLSTDKMSLNYRLFPDRIRQLFGDVVRAEKDLDYWHFDMMGQTMLIRNAEGDYTPAHRSLLEFFVAYKFAAELGTLAEDFTELAQAQSHLDKSAAPQDYTWSSYFQQRMDETGKILRTPPLQKFAPENIANLHSSFGQVLLTKAVIDLLLPMLIPLPNEETMSFSYPLFNILELTREKSRSEVGFICANVVMLLAKLNSNALKDKDINSSFLSNTSFSSADLSNTNLSYANLSNADLSNTNLSYANLSNADLSNTNLSNANLSDANLSNANLSNANLDDANLTGADLSHSIIRGASFKGTNISGTNLQNVTR
>NZ_CP019636.1|WP_087540473.1|3289924_3290986_-|alpha/beta-fold-hydrolase
MCDSSYSPSRFLQNGVVMTVYTALWASRDWEHTTNSPEPLYQEKIFVGAQGVPIFGWVAIPKNAHSTIVGTYGITGDLHNQWYLRLLGRKAFAQGYAVVLFDWRAHGKTAQLSPTLTSDGLYEGEDFVRIAATAKAMGCPGKFWFTGYSLGGQLALWAVKAAAEFIKEDENLGLEDSDIGGAAVICPSLDSLRSLSFLVKHPVGKYFERAIARQLKKLAWQIHDAHPGSFDTEAIERANSIWGFDEELVIGRLGFPTVDAYYEATSALPLLPNLTKPTLIIYAEDDPFFEPAIIPELQAACARNPKIDLLLTRHGGHVGYISSQECQRQAQDPDKWWAWNRILEWIDKHGQEY
>NZ_CP019636.1|WP_087540475.1|3291143_3291887_+|response-regulator-transcription-factor
MPRILVIDDDPAISELVAVNLEMAGYDVSQAEDGIKGQALALQLQPDLIMLDLMLPRVDGFTVCQRLRRDDRTAEIPVLMLTALSQTQDKVEGFNAGADDYLTKPFEVEEMLARVRALLRRTDRIPQAAKHSEILNYGPLTLVPERFEAIWFGQTVKLTHLEFELLHCLLQRHGQTVSPSEILREVWGYDPDDDIETIRVHIRHLRTKLEPDPRHPRYIKTVYGAGYCLELPSIPQSTEGASTTSGV
>NZ_CP019636.1|WP_157679443.1|3292231_3292483_+|hypothetical-protein
MGYALLTHPTFIYVQLLIPQYGSVKAQSSIDDMKRPLWVSPVLQEVRPVLQEGNPAVGNWRSRSVSVGFTRKGHKTCKGKQRR
>NZ_CP019636.1|WP_087540477.1|3292545_3293598_-|UDP-3-O-(3-hydroxymyristoyl)glucosamine-N-acyltransferase
MKFSEILEKLGNAASNSSLCSNKDQDPEITGVAAVDEAITGNLSYIEGARFASMVSQTSASALILPVDETLQTQAQERGIVWIATPEPRLLFAKVITLFYQPWRPTAEIHPTAVIHPTVKIGHGVYVGPHAVIQQGVEIGNDVCIHPNVVIYPDVKIGDRTTLHANCTIHERSRIGADCMIHSGAVIGAEGFGFVPSSRGWIKMEQSGYTVLEDGVEVGCNSAIDRPAVGETRIGRNTKIDNLVQIGHGCQIGSGCALAGQSGMAGGVKLGNGVILAGQSGIANQVKIGDQAIASAKAGIHNDVAPGEIVSGSPALPHKQYLKVSAVLGRLPEMYQALKQLQRKLNNGND
>NZ_CP019636.1|WP_087540479.1|3293797_3295150_-|murein-transglycosylase-A
MRKTLTLASLSLGIALVNPIWSVFAQQVPYLPPIPIPVPSQPEISPPPQPSQPEEVSPALVPVDIETLCNSLYSCPGWDEQIWGGNGKLGDAEPRTLKSDNAGRPTRGDDAQRSTGGDRRALLTAIDNSLRYLTTDKAVAAYQNYPIKQISLERVRRSLQRFRQLVVSSESPAQLQAAVRREFVFYQSVGNDGNGNVKFTAYYEPVYAASRVRTSVYKYPIYRLPPDFDKWAKPHPKRVELEGKNGLLGNKSPLRGLELFWFRNRLDAYLIQIQGSAQLKLTNGTTTSVGYAGGTDYPWTSIGGELAKDGKLPLKGLTMPVLIQYFQQNPKEMNNYLPRWERFVFFKETGGTPATGSIRVPVTPERSIATDKSVMPPGALALINTSVPYPAGGGQLVHRTVNRYVLDQDTGSAIKGPGRVDYFMGSGKLAGDRAGVTGGNGKLYYLLLKD

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Crispr_ID: NZ_CP019636_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_9

4115463-4118049

TypeI-D,TypeV

I-D,II-B

Consensus_repeat	Method
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CRISPRCasFinder
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CRT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	PILER-CR

35 spacers

cas14k,cas6,2OG_CAS,csc1gr5

The CRISPR arrays of NZ_CP019636_9

>merge|NZ_CP019636|9|4115463-4118049|CRISPRCasFinder,CRT,PILER-CR
CCTTTAATCCCTGATAGGGATTCATAATAATTGTAACGCCTTAGCAATTTCCTCAACAATCCTGCGAATATTTGCCCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACAGCTAAAGATTCTGGCATTAGTCGCACTCATTGGGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTTTTTCTTATTTAACAATAAATTTGGAATCTGCCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACGGCAGTACGTCTACCTCACCAACAATGTGGAATCCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACGCTAAGCACTTAACATCTTGCCAGAAAGATCCAGTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACAAGTGTTTTGATAATGCTTTTTAGTAGTGTATTTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACCATTTTGTATACGAGATTTACGGCAAACTCATTCTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACCGTACTGTGTTTAAGTGGCGTCCTATTGCTGATTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTGATTCCCCATGCGCTCTTTATCCAACCACGTTTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTGCCTGCCAATGATGTAGCATTGCTTCCACAAATTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTTTGCTTAGCTGATATAGACAAATATATACTCGTTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTTATAACGCGGTCGCTACCTCTGCTAATTGCCACATAATGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACCATACCGCAACAACTTACGGTAGCACAACATATCCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACGCTATGTTGCCTACACCGACGTTGAAATTGATATACCTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACAACCCGCAAACCCAGACTTTGAGGAATTGGTACAGAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACATACGTATATCTCTGCATTACTACTAGTGACTTCAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACATAATCTTGAAAGTGTGACTTTTTGCCGTTCCCGGATTGCCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACACAGAATCCAAGCAAAAACTCTTACAAACATTTGCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCTCCCAAAGATGCACCGAAACCCGCTCCTATCTTTTTTTCAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACCTTAGAGTCTGTCCGTGGTCGGGTAGAGACAGTAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCTACTTGAAAACCGAGTCTGACCGGAAATACCTTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCTACAATAGTCTGTTTAGCACTGTCAGTAAATAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACGTCTATGTGCGCCGCAAATATCTCTGACTCCTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACGGTTGGTCATGGGCAAATATACCACTAACTGTATTTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACCTGGAAATGTACGTGTCTTGCGCCTTTCTCTATCCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACAACGTTGCGTGTTTTTTTCACAGTATCCAGAAGTTCTAAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACGTTGGTTACTTTGGTGAAATTGATATTGAACAGATTAGTGGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTAGCTGCCCAAGCGCGATATACCTTGGACTTTGAAAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCTATTTTCTTTGGCTACAAAACTGAAAGAGTAGTAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCGCTGCATTATCAGAGGGCGAAATGGTTTTAAACGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTTTTTACTTGTTGTGCATTTCTTTTTCATATTCTTGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCACTTGCTTTCACTTGCACTTGAGGCGGAAGAAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTGGCGCAAGTCGTTACGGAGCAGTTACGGATCAAGTGCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCTATGACTTCCCATCTGCCCGCTGCCTCACCCGCGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAACTCCTCATTGTTGAGGTAGGAAAAAAGTGCTTGGTAGTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC

>NZ_CP019636|9|9|4115463-4118049|CRISPRCasFinder
CCTTTAATCCCTGATAGGGATTCATAATAATTGTAAC	GCCTTAGCAATTTCCTCAACAATCCTGCGAATATTTGCCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AGCTAAAGATTCTGGCATTAGTCGCACTCATTGG
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTTTCTTATTTAACAATAAATTTGGAATCTGCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GGCAGTACGTCTACCTCACCAACAATGTGGAATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GCTAAGCACTTAACATCTTGCCAGAAAGATCCAGT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AAGTGTTTTGATAATGCTTTTTAGTAGTGTATTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CATTTTGTATACGAGATTTACGGCAAACTCATTCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CGTACTGTGTTTAAGTGGCGTCCTATTGCTGATT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGATTCCCCATGCGCTCTTTATCCAACCACGTTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGCCTGCCAATGATGTAGCATTGCTTCCACAAATT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTGCTTAGCTGATATAGACAAATATATACTCGTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTATAACGCGGTCGCTACCTCTGCTAATTGCCACATAAT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CATACCGCAACAACTTACGGTAGCACAACATATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GCTATGTTGCCTACACCGACGTTGAAATTGATATACCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AACCCGCAAACCCAGACTTTGAGGAATTGGTACAGA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ATACGTATATCTCTGCATTACTACTAGTGACTTCA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ATAATCTTGAAAGTGTGACTTTTTGCCGTTCCCGGATTGCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ACAGAATCCAAGCAAAAACTCTTACAAACATTTGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTCCCAAAGATGCACCGAAACCCGCTCCTATCTTTTTTTCA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CTTAGAGTCTGTCCGTGGTCGGGTAGAGACAGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTACTTGAAAACCGAGTCTGACCGGAAATACCTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTACAATAGTCTGTTTAGCACTGTCAGTAAATA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GTCTATGTGCGCCGCAAATATCTCTGACTCCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GGTTGGTCATGGGCAAATATACCACTAACTGTATTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CTGGAAATGTACGTGTCTTGCGCCTTTCTCTATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AACGTTGCGTGTTTTTTTCACAGTATCCAGAAGTTCTAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GTTGGTTACTTTGGTGAAATTGATATTGAACAGATTAGTG
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TAGCTGCCCAAGCGCGATATACCTTGGACTTTGAAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTATTTTCTTTGGCTACAAAACTGAAAGAGTAGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCGCTGCATTATCAGAGGGCGAAATGGTTTTAAAC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTTTACTTGTTGTGCATTTCTTTTTCATATTCTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCACTTGCTTTCACTTGCACTTGAGGCGGAAGAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGGCGCAAGTCGTTACGGAGCAGTTACGGATCAAGTGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTATGACTTCCCATCTGCCCGCTGCCTCACCCGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCCTCATTGTTGAGGTAGGAAAAAAGTGCTTGGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC

>NZ_CP019636|9|1|4115463-4118049|CRT
CCTTTAATCCCTGATAGGGATTCATAATAATTGTAAC	GCCTTAGCAATTTCCTCAACAATCCTGCGAATATTTGCCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AGCTAAAGATTCTGGCATTAGTCGCACTCATTGG
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTTTCTTATTTAACAATAAATTTGGAATCTGCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GGCAGTACGTCTACCTCACCAACAATGTGGAATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GCTAAGCACTTAACATCTTGCCAGAAAGATCCAGT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AAGTGTTTTGATAATGCTTTTTAGTAGTGTATTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CATTTTGTATACGAGATTTACGGCAAACTCATTCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CGTACTGTGTTTAAGTGGCGTCCTATTGCTGATT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGATTCCCCATGCGCTCTTTATCCAACCACGTTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGCCTGCCAATGATGTAGCATTGCTTCCACAAATT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTGCTTAGCTGATATAGACAAATATATACTCGTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTATAACGCGGTCGCTACCTCTGCTAATTGCCACATAAT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CATACCGCAACAACTTACGGTAGCACAACATATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GCTATGTTGCCTACACCGACGTTGAAATTGATATACCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AACCCGCAAACCCAGACTTTGAGGAATTGGTACAGA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ATACGTATATCTCTGCATTACTACTAGTGACTTCA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ATAATCTTGAAAGTGTGACTTTTTGCCGTTCCCGGATTGCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ACAGAATCCAAGCAAAAACTCTTACAAACATTTGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTCCCAAAGATGCACCGAAACCCGCTCCTATCTTTTTTTCA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CTTAGAGTCTGTCCGTGGTCGGGTAGAGACAGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTACTTGAAAACCGAGTCTGACCGGAAATACCTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTACAATAGTCTGTTTAGCACTGTCAGTAAATA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GTCTATGTGCGCCGCAAATATCTCTGACTCCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GGTTGGTCATGGGCAAATATACCACTAACTGTATTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CTGGAAATGTACGTGTCTTGCGCCTTTCTCTATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AACGTTGCGTGTTTTTTTCACAGTATCCAGAAGTTCTAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GTTGGTTACTTTGGTGAAATTGATATTGAACAGATTAGTG
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TAGCTGCCCAAGCGCGATATACCTTGGACTTTGAAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTATTTTCTTTGGCTACAAAACTGAAAGAGTAGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCGCTGCATTATCAGAGGGCGAAATGGTTTTAAAC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTTTACTTGTTGTGCATTTCTTTTTCATATTCTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCACTTGCTTTCACTTGCACTTGAGGCGGAAGAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGGCGCAAGTCGTTACGGAGCAGTTACGGATCAAGTGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTATGACTTCCCATCTGCCCGCTGCCTCACCCGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCCTCATTGTTGAGGTAGGAAAAAAGTGCTTGGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC

>NZ_CP019636|9|1|4115540-4118049|PILER-CR
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AGCTAAAGATTCTGGCATTAGTCGCACTCATTGG
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTTTCTTATTTAACAATAAATTTGGAATCTGCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GGCAGTACGTCTACCTCACCAACAATGTGGAATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GCTAAGCACTTAACATCTTGCCAGAAAGATCCAGT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AAGTGTTTTGATAATGCTTTTTAGTAGTGTATTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CATTTTGTATACGAGATTTACGGCAAACTCATTCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CGTACTGTGTTTAAGTGGCGTCCTATTGCTGATT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGATTCCCCATGCGCTCTTTATCCAACCACGTTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGCCTGCCAATGATGTAGCATTGCTTCCACAAATT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTGCTTAGCTGATATAGACAAATATATACTCGTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTATAACGCGGTCGCTACCTCTGCTAATTGCCACATAAT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CATACCGCAACAACTTACGGTAGCACAACATATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GCTATGTTGCCTACACCGACGTTGAAATTGATATACCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AACCCGCAAACCCAGACTTTGAGGAATTGGTACAGA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ATACGTATATCTCTGCATTACTACTAGTGACTTCA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ATAATCTTGAAAGTGTGACTTTTTGCCGTTCCCGGATTGCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	ACAGAATCCAAGCAAAAACTCTTACAAACATTTGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTCCCAAAGATGCACCGAAACCCGCTCCTATCTTTTTTTCA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CTTAGAGTCTGTCCGTGGTCGGGTAGAGACAGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTACTTGAAAACCGAGTCTGACCGGAAATACCTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTACAATAGTCTGTTTAGCACTGTCAGTAAATA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GTCTATGTGCGCCGCAAATATCTCTGACTCCT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GGTTGGTCATGGGCAAATATACCACTAACTGTATTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	CTGGAAATGTACGTGTCTTGCGCCTTTCTCTATCC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	AACGTTGCGTGTTTTTTTCACAGTATCCAGAAGTTCTAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	GTTGGTTACTTTGGTGAAATTGATATTGAACAGATTAGTG
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TAGCTGCCCAAGCGCGATATACCTTGGACTTTGAAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTATTTTCTTTGGCTACAAAACTGAAAGAGTAGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCGCTGCATTATCAGAGGGCGAAATGGTTTTAAAC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TTTTTACTTGTTGTGCATTTCTTTTTCATATTCTT
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCACTTGCTTTCACTTGCACTTGAGGCGGAAGAA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TGGCGCAAGTCGTTACGGAGCAGTTACGGATCAAGTGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCTATGACTTCCCATCTGCCCGCTGCCTCACCCGC
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC	TCCTCATTGTTGAGGTAGGAAAAAAGTGCTTGGTA
GTTTCAATCCCTGATAGGGATTCGTAGTAATTGTAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087546224.1\|4112049_4112592_-\|peroxidase-related-enzyme	unknown	unknown	gnl\|CDD\|130981
NZ_CP019636.1\|WP_087546223.1\|4110745_4112032_-\|adenylate-cyclase	unknown	unknown	gnl\|CDD\|143636
NZ_CP019636.1\|WP_087546221.1\|4107096_4107684_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_157679520.1\|4110546_4110687_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546222.1\|4109278_4110430_+\|M28-family-peptidase	unknown	unknown	gnl\|CDD\|349893
NZ_CP019636.1\|WP_087541345.1\|4103500_4104889_+\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	cas14k	-	gnl\|CDD\|273793
NZ_CP019636.1\|WP_087541347.1\|4105954_4106953_+\|UDP-glucose-4-epimerase-GalE	unknown	unknown	gnl\|CDD\|224012
NZ_CP019636.1\|WP_087541353.1\|4121870_4122320_-\|nucleotidyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|376187
NZ_CP019636.1\|WP_087541346.1\|4105011_4105701_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541350.1\|4118372_4119218_-\|CRISPR-associated-endoribonuclease-Cas6	cas6	COG5551_cas6_CAS-III	gnl\|CDD\|227838
NZ_CP019636.1\|WP_087541354.1\|4122370_4122583_-\|DUF433-domain-containing-protein	unknown	unknown	gnl\|CDD\|225291
NZ_CP019636.1\|WP_087546225.1\|4121434_4121869_-\|DUF86-domain-containing-protein	unknown	unknown	gnl\|CDD\|366864
NZ_CP019636.1\|WP_087541356.1\|4128315_4129713_-\|ATP-grasp-domain-containing-protein	unknown	unknown	gnl\|CDD\|235876
NZ_CP019636.1\|WP_087541355.1\|4124013_4128021_-\|non-ribosomal-peptide-synthetase	unknown	unknown	gnl\|CDD\|237108
NZ_CP019636.1\|WP_087541357.1\|4129923_4130760_-\|SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|366722
NZ_CP019636.1\|WP_157679522.1\|4128176_4128347_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541348.1\|4107688_4108912_-\|ferric-reductase	unknown	unknown	gnl\|CDD\|225392
NZ_CP019636.1\|WP_087541352.1\|4119988_4120570_-\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	csc1gr5	cd09711_csc1gr5_CAS-I-D	gnl\|CDD\|187842
NZ_CP019636.1\|WP_087541351.1\|4119195_4119828_-\|2OG-Fe(II)-oxygenase	2OG_CAS	-	gnl\|CDD\|379309
NZ_CP019636.1\|WP_087541349.1\|4112891_4114202_+\|M24-family-metallopeptidase	unknown	unknown	gnl\|CDD\|182804

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087546224.1\|4112049_4112592_-\|peroxidase-related-enzyme	gnl\|CDD\|130981	TIGR01926, peroxid_rel, uncharacterized peroxidase-related enzyme. This protein family with length of about 200 amino acids. One member, from Myxococcus xanthus, is a selenoprotein, with an otherwise conserved Cys replaced by Sec. This family is drawn narrowly enough to suggest that These proteins contain a domain described by TIGR00778, with a CxxCxxxHxxxxxxxG motif. Some members of that family are known to act as peroxidases or correlate with resistance to oxidative stress.	3.4178e-20
NZ_CP019636.1\|WP_087546223.1\|4110745_4112032_-\|adenylate-cyclase	gnl\|CDD\|143636	cd07302, CHD, cyclase homology domain. Catalytic domains of the mononucleotidyl cyclases (MNC's), also called cyclase homology domains (CHDs), are part of the class III nucleotidyl cyclases. This class includes eukaryotic and prokaryotic adenylate cyclases (AC's) and guanylate cyclases (GC's). They seem to share a common catalytic mechanism in their requirement for two magnesium ions to bind the polyphosphate moiety of the nucleotide.	2.16685e-63
NZ_CP019636.1\|WP_087541348.1\|4107688_4108912_-\|ferric-reductase	gnl\|CDD\|225392	COG2836, COG2836, Uncharacterized conserved protein [Function unknown].	3.30452e-52
NZ_CP019636.1\|WP_087546222.1\|4109278_4110430_+\|M28-family-peptidase	gnl\|CDD\|349893	cd05640, M28_like, M28 Zn-peptidase; uncharacterized subfamily. Peptidase family M28 (also called aminopeptidase Y family), uncharacterized subfamily. The M28 family contains aminopeptidases as well as carboxypeptidases. They have co-catalytic zinc ions; each zinc ion is tetrahedrally co-ordinated, with three amino acid ligands plus activated water; one aspartate residue binds both metal ions.	8.76865e-66
NZ_CP019636.1\|WP_087546225.1\|4121434_4121869_-\|DUF86-domain-containing-protein	gnl\|CDD\|366864	pfam01934, DUF86, Protein of unknown function DUF86. The function of members of this family is unknown.	3.49907e-21
NZ_CP019636.1\|WP_087541347.1\|4105954_4106953_+\|UDP-glucose-4-epimerase-GalE	gnl\|CDD\|224012	COG1087, GalE, UDP-glucose 4-epimerase [Cell envelope biogenesis, outer membrane].	0
NZ_CP019636.1\|WP_087541353.1\|4121870_4122320_-\|nucleotidyltransferase-domain-containing-protein	gnl\|CDD\|376187	pfam18765, Polbeta, Polymerase beta, Nucleotidyltransferase. A member of the nucleotidyltransferase fold found in polymorphic toxins (NTox45) and polyvalent proteins.	1.7885e-20
NZ_CP019636.1\|WP_087541350.1\|4118372_4119218_-\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|227838	COG5551, COG5551, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	8.34236e-54
NZ_CP019636.1\|WP_087541354.1\|4122370_4122583_-\|DUF433-domain-containing-protein	gnl\|CDD\|225291	COG2442, COG2442, Uncharacterized conserved protein [Function unknown].	3.10289e-23
NZ_CP019636.1\|WP_087541356.1\|4128315_4129713_-\|ATP-grasp-domain-containing-protein	gnl\|CDD\|235876	PRK06849, PRK06849, hypothetical protein; Provisional.	0
NZ_CP019636.1\|WP_087541355.1\|4124013_4128021_-\|non-ribosomal-peptide-synthetase	gnl\|CDD\|237108	PRK12467, PRK12467, peptide synthase; Provisional.	0
NZ_CP019636.1\|WP_087541357.1\|4129923_4130760_-\|SAM-dependent-methyltransferase	gnl\|CDD\|366722	pfam01596, Methyltransf_3, O-methyltransferase. Members of this family are O-methyltransferases. The family includes catechol o-methyltransferase, caffeoyl-CoA O-methyltransferase and a family of bacterial O-methyltransferases that may be involved in antibiotic production.	1.74409e-55
NZ_CP019636.1\|WP_087541345.1\|4103500_4104889_+\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl\|CDD\|273793	TIGR01766, Putative_transposase_MJ0751, transposase, IS605 OrfB family, central region. This model represents a region of a sequence similarity between a family of putative transposases of Thermoanaerobacter tengcongensis, smaller related proteins from Bacillus anthracis, putative transposes described by pfam01385, and other proteins. [Mobile and extrachromosomal element functions, Transposon functions].	3.00983e-07
NZ_CP019636.1\|WP_087541352.1\|4119988_4120570_-\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	gnl\|CDD\|187842	cd09711, Csc1_I-D, CRISPR/Cas system-associated protein Csc1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; RAMP superfamily protein; predicted Cas5 ortholog; also known as CasA/Cse1 family.	2.35601e-69
NZ_CP019636.1\|WP_087541351.1\|4119195_4119828_-\|2OG-Fe(II)-oxygenase	gnl\|CDD\|379309	pfam13640, 2OG-FeII_Oxy_3, 2OG-Fe(II) oxygenase superfamily. This family contains members of the 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase superfamily.	1.13352e-08
NZ_CP019636.1\|WP_087541349.1\|4112891_4114202_+\|M24-family-metallopeptidase	gnl\|CDD\|182804	PRK10879, PRK10879, proline aminopeptidase P II; Provisional.	1.27078e-155

>NZ_CP019636.1|WP_087541349.1|4112891_4114202_+|M24-family-metallopeptidase
MQAEYRQRREQLMSKIGSGTAIFRSAPTAVMHNDVEYTFRQDSDFYYLTGFNESQAVAVLAPSHPEHRFVLFVQPKVREQEVWSGYRCGVEAAKQVYGADEAYPITELDEKLPQYLEKADRIYYHLGRDRSFNETILNHWQRLMRAYPKRGTGPIAIEDTGPILHSMRLVKSQAELEQMRKAADIAVEAHNRAMEFTQPGRYEYEVQAEIEHIFRLRGGMGPAYPSIVASGVNACVLHYIENNRQMQDKELLLIDAGCAYGYYNSDITRTFPVSGKFTPEQKTLYEIVLEAQKQAIAQVQPGNPYKQIHDTAVRVLTEGLVEVGILKGEVDKLIEEEKYKPYYMHRTGHWLGLDVHDVGVYQHGDDKPQILQPGQVLTVEPGLYIVPDTKLAEDQPETDPRWVGIGIRIEDDVLVTATGHEVLTAGVPKEVAEVEK
>NZ_CP019636.1|WP_087546224.1|4112049_4112592_-|peroxidase-related-enzyme
MAKFPIMKYEQLTNSQVKTIYQEIQIELGFGIVPNLFKSMAINPEVLEANWKKFRATLLKGDVPRTLKEMLGIAISQANNSPYALNVHLHGLSSLGMSEEVLKTLVSDFAACPLPQREKAVIRFGLKAANEPHKLTDEDYQYLYKLGLNDSEIFEIIATADLFTSINRYTDSISLEIDTL
>NZ_CP019636.1|WP_087546223.1|4110745_4112032_-|adenylate-cyclase
MDSRLEEQDYQQLLLLSRRLLAEAQAFSSRIAAVNEIAIAMNRSLNMDNILQVVGKHAKWLLDFEHCSVCLRNTNNSSWRIVTLFGPVGKIDSFDITDIGVVGLSLKQGQAQLIHENSTSGFLSQYQSQIIIPLENENQVIGTINFAITPPRSYTQEDLRIGYLLAVQLSAAITNAKRFEELNGLYIQLEEEKRKTDQLLLNILPTDIAAELKQTGTVKPVYYECASVLFTDFKNFTKLTEQLSPQELVDELDYCFSCFDQFIEAHNLEKLKTIGDSYMCVGGIPTPNKTHAIDAVLAAINIRTFMEWRKKEKALLKQPYWEIRIGIHSGPLLAGVIGHKKFAYDVWGDTVNTASRLELSGVPGSINISQATFELIKDFFAVQYRGKITAKNKGEIDMYFVEGIKSNLALDPTGLLPNNKFNQLYFAI
>NZ_CP019636.1|WP_157679520.1|4110546_4110687_-|hypothetical-protein
MLSFIIHAVIKGRPHPCILEKVDFHPPVPLVQRQQGTGKTTRYSVV
>NZ_CP019636.1|WP_087546222.1|4109278_4110430_+|M28-family-peptidase
MKKWFWLVLLLVTVVAIALTSEFVKQHRESVIYSIRVENSPTTHQDKTQTGQDVQTTRRKQTNIENSPTSEPLQVPKSLQVSADKLFAHIQRLNFTRHTPAERSRTRAYITSELKQLGWKPKLEKFQDGVNVFAQRPGTDKNAGIILIAAHYDTVYNSPGADDNATGVAVVLEVARLLGSRPTPRTLQLAFFDLEEAGLLGSKAFVTNKKYLENLDGVIVIDMVGFACHTPGCQKYPTGLPIAPPSDKGDFLAVVGDTEHLPLLNAFQNSQKFPAISFNKAMIRESSLPAVLTLPIPLKGLLTPDTLRSDHAPFWYQGVGAVLVTDTANLRTPHYHQPSDVPATIDRKFFTGAAQVIVNTTHVLLENSHSLDSSPSTLQTPSG
>NZ_CP019636.1|WP_087541348.1|4107688_4108912_-|ferric-reductase
MLHLLLIMTLGFVGSFGHCFGMCGPLAVAFSLSHKQDSHWQQQLQFHALLNLGRMLSYVLVGAGIGALGSVLLASGQMAGIGSELRHWMAIITGVLLIWFGIGQIKSDFLPRIPLLHPLMQGRLHNSLSQAMVRLSQQTKWWTPALLGMTWGLMPCGFLYAAQIKAAETGNWLIGAATMLAFGLGTLPTMLGVGVSTSLVSKDKRSQLFRLGGWVTLTIGVLTLLRTGDTMVDYTGHAALICLILALVARPINRLWAAPLRYRRALGVGAFVLSLAHTTHMMEHSLQWNIAAFLFLPPDYQLGMALGAMALVLMIPAALTSFDNLQKCLGDRWRAIHLLSVPALLLSAIHAVIIGSHYLGSFQSTWENKLATVLLGFVTLAVILVRWRFFWSILSLQKFYVPPKRSQ
>NZ_CP019636.1|WP_087546221.1|4107096_4107684_-|hypothetical-protein
MYQGLKSLTFIVIYAASTYPAVAHKVTTATDVGATLHIEPNDNPRAGESTKTWFAMTRKGGKVIPLAECNCQLAVYAEPHSANEPPLIEPPLKPISAERYQGIPGTEITFPRPGAYQLHLSGKPKNGKSFQPFDLKFPVTVAAGSVTTDSTQKIQNVNDSITQGQTQGIPLWAIALSGLLAVGVFFGILRMVKRR
>NZ_CP019636.1|WP_087541347.1|4105954_4106953_+|UDP-glucose-4-epimerase-GalE
MSPGKPTILVTGGAGYIGSHTVLALKQAGFDVIILDNLVYGHRDLVEKVLQVELVVGDTGDRALLDDLFKTRDVAAVMHFSAYAYVGESVTDPAKYYRNNVIGTLTLLEAMLAASVKKFVFSSTCATYGVPQVVPIPEDHPQNPINPYGATKLMVERILSDFHVAYDFKSVRFRYFNAAGAAPNGLLGEDHNPETHLIPLVLQTALGKRESISVFGTDYPTPDGTCIRDYIHVSDLADAHVLGLKYLLEGGDSQVFNLGNGNGFSVKEVIETAKKVTGKDIKVVECDRRPGDPPALIGSGDKARQILGWHPQYPSLEEIITHAWQWHQSRHK
>NZ_CP019636.1|WP_087541346.1|4105011_4105701_-|hypothetical-protein
MFELLSRVLLWLLVGTIIYTLFQRFYPSGTFVGRLVLVIMLLVILLSFINPNEPAVASLWRVVSFPLKPLGASILLMVFAAQRMKKGGTLDAPGGYLIGWALTILLLSSTPAFAYFLVRSPVAMVGEPYLANQEIVQNVRLASSIAPATSTSETLVALGQNSTITSDGIISASRMSDVVSAPYLLQTPQDIRRRGLRLEDFVPNAEMLQITTRVWETYLNQIYFFLRGR
>NZ_CP019636.1|WP_087541345.1|4103500_4104889_+|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MYRTIPVKARFTDEEKAFWVDQCEHANSLINSAIYHVKQTHYSRLEQTDDAFTTYWRGDELRYGWKTYKCSTTYPELDKVLKDNPHYKAMAAQSAQQTLKAVGESITSYNGLVNAYYKGEVDRPSLPKYRKRGGLAAVTFPRQALNYKDGCFYPSISRDTKPHLLTEITLQLPEFIDSDWVKEVTVRPCLGELWIDWVIDDGKEPIGNNPKLDYTQAWSFDHGGTNWLTGVSTRGKSLIIDGRKLKSMNQGYCHLVAKYKQGKSDFYWDANLDRVQRKRNNQMRDAVNKAARFIINQCLNDCVGNLVIGWNDGQKNGSNMGKRGNQNFVVIPTKRLIDRLKQLCPEYGIVLTITEEAYTSKASYLDGDSLYKHGEKPAGWKPSGNRVKRGLYKSRDGHVINADCNGAANIARKVATQLGLNLAKLGRGALTLPRRVDLFKGLSKSYRKRCGAGLLDPVATSV
>NZ_CP019636.1|WP_087541350.1|4118372_4119218_-|CRISPR-associated-endoribonuclease-Cas6
MPHSLVLNLLPKCSIIPQFLTGRHLHALFLTLVSSVDRELGDRLHDSSADKAFTISPLQVKLNHTSRNKISDHTLQWEHEKPIPAGTTCWWRISLLDDTLFSKLTQLWLNLNPTHSWHLGPADLYITSILGTPESRQPWASAATYTQLYEQASDSERQIAFSFCTPTNFRQGHFDTALPTRECVFNSLLQRWNKYSGISLEPNLTEVIFPSFFNIRTAITADSRSKFIGCVGEINYRILGNIDPLIIKQINALANFALYCGAGRKTTMGMGMIRRLNMTQC
>NZ_CP019636.1|WP_087541351.1|4119195_4119828_-|2OG-Fe(II)-oxygenase
MKYYHQQPNAFPSNYLNDLRGQIQACPYFAINNLNRDFVATKGFSVVFQRSGLAQVEEQFPYFKPYLDLALQPNCNAFYLNPLQMKEGSRVDPHIDRSLRSYCKTIEPPMLVSVLYVWVPSEMEGGELVLRSRKRQVGFIKPQMNTLLYFQGDLTHSVNAVKTPGNRLSLVCEQYSLSDTELREIPQFTLESRANQYTTQKRKYASQPCA
>NZ_CP019636.1|WP_087541352.1|4119988_4120570_-|type-I-D-CRISPR-associated-protein-Cas5/Csc1
MVDSEIYSTTVSEEHSYRYFCSEQVPKYEEHLTPLNQQGIYVTPARSISHAAILNTWKYANNNYHVEMEKTQKNIPSFGRAKEIAPESQFEFFVISQKEIKLPKWIRLGKWMSKAEVISEQLPKPKTTEGVFTCVHSLNPLDIMFTNQVMSYDVVNMSPVSLIQNVQMQGQYYYFDDIKNLKIPVRMEYRFRG
>NZ_CP019636.1|WP_087546225.1|4121434_4121869_-|DUF86-domain-containing-protein
MDLEVVLVRLRLIVKYCNTLEEFRSITLNEYLGNFHQQLIVERLLQLVVEAATDINKYLLVQLHKISPATNFDSFTEAGRQSIITQDLATKLAQSVGMRNILVHQYKDIDNKIVFSAIPKALEQYRFYVQQVTVYLNSLEAEDG
>NZ_CP019636.1|WP_087541353.1|4121870_4122320_-|nucleotidyltransferase-domain-containing-protein
MNTPTIEELRELAQQIPEKIPYLKMLVLFGSRATGKTHANSDWDFAVLCDEEERKNHTKDNDWSWFEIPLLLGDIFRINHEQIDVVELNNCSWLIAHFVARDGILLYEKDRGGFEYFRLTSLRPESEMKKFRQDQRQLIDMELKKWGYE
>NZ_CP019636.1|WP_087541354.1|4122370_4122583_-|DUF433-domain-containing-protein
MDEQQLLQRITLNPKIFGGKPIIRGRRLAVEHILGMLAAGDTIETLLKGYSWLEREDVQACLVYTHRERN
>NZ_CP019636.1|WP_087541355.1|4124013_4128021_-|non-ribosomal-peptide-synthetase
MDTTQAHPISNAEAITEFSLTHAQQVAWFLYKFAPQSYIDKLAFAVRFSQQLDYECLDRVFQSLVKRHPSLRTAYIEKQGKVLQHVVDEASASVDFVSSTGWNEEKLQNQVLQSLQRPFDLASGSVVRLSVFSCTPTNHVILLAVHQIACDDRTLMLLVDELLKLYQARKNNIVIALPSVDSSYQEYVQRELNLLNSPEGEQLWYELKGRLDGELPTLNLPMSRPRPPVRTYRGALHKFCISPNIASKLQQFAQTEDVELSTILLAAFQVILHRYTATEELLVGFKTEQAKSRNFNCKIGNFNNLTVVRSSISSTLSFQELLSLTRSAVFDVIAHQDYPFPLLVRQLQLNSQLSHPPICQVGLTYQNLDKLETLSTLFNQTNSSLSYFEIPEQRVEFDLNWEILEAGESLTCFLHYNRDLLDADAIVRMAGQLQILLAEIVTSPKQQVTQLPILTDSEQHQLLIEWNATHRDYNLSRCLHELFETQVDLTPEAIAVSFEQQQLTYRELNEKANQLAHHLQKKGVKTEVLVGISVERSLQMVIGLLGILKAGGAYVPIDPESPQERIAYMLADSQVSLLLTQKKQVTQLPKSQAQIICLDADWEKISQEQTNNPASGVQPENLAYVIYTSGSTGKPKGAMNTHRGICNRLLWMQEAYQLTATDAVLQKTPFSFDVSVWEFFWTLLTGARLVIAKPGGHRDRSYLVELISQEQITTLHFVPSMLQVFLESRDLDKCQSLRRVICSGEALTLDLQEKFFQHLGCELHNLYGPTEAAIDVTFWRCQRQSHLRTVPIGRPIANTQIYILDPHLQPVPIGVTGELYIGGVGVARGYLNREELTAECFITNPFRQSDRLYKTGDLARYLSDGNIEYIGRIDHQVKIRGFRVELGEIENALSQHPQVREAVVIVRQDKPGDKQIVAYIVSTENLPSPSLLREFLRQKLPDYMVPAAFILLETLPLTSNGKLDRRALPSPSLSNFSESHNYIAPRNDIEQQLAEIWAQILDVHPVGVRDNFFELGGNSLLAIHLIAEIEEKFGKDLPLSELLTNPVIEDLAKILQTASNIFNNSPIVPIQPKGNKRPFFCVHPAGGHVFCYFNLARYLGREQPFYGLQAQGFNGEEEPLSRVEDMASLYVKAIQTVQPEGPYQIGGWSFGGVVAYEVAQQFYKQGHEVSLLAILDSYVPIVLDKQKEINNQYLVGVLSRVFGGMFGQDNLVTQDEIKHLSVDEQIDYIIDKARKVKIFPPTVERRKNRRILDVLVGTLKATYSYVRQPYPGKATIFRAREKHIMAPDPTLVWVELFSIMAAKEIEIIDVPGSHYSFVLEPHVQVLAERLKTCLV
>NZ_CP019636.1|WP_157679522.1|4128176_4128347_-|hypothetical-protein
MANWWNWAVIEPGNQFDQTTDEQRTLASPDGEASPTSIDVYLWFLLDLFAFLQEVY
>NZ_CP019636.1|WP_087541356.1|4128315_4129713_-|ATP-grasp-domain-containing-protein
MAHSISLSSRPATPAISIKALLVALFQNLGTLTILLLVLPINAAIVLISLLWSRLSSPWRSQKAVVATHRKNILISGGKMTKALQLARSFHAAGHRVVLIETHKYWLSGHRFSNAVSRFYTTPTPQHNPEAYIQALLDIVKREKIDVYVPVTSPVASYYDSLAKPALSPYCEVFHFDADVTQMLDDKFAFSEKARALGLSVPKSFKITNPEQVINFDFSQETRKYILKSIPYDSVRRLDLTKLPCDTPEETAAFVRSLPISPEKPWIMQEFIPGKEFCTHSTVKNGELRLHCCSESSAFQVNYENIENPKIQKWVTHFVKELGITGQISFDFIQAEDGTVYAIECNPRTHSAITMFYNHPQVADAYLSQEAFTEPQEPLPNSKPTYWTYHEVWRLTGIRSFAQLQTWIRNFLRGKDAIYQVDDPLPFLMVHHWQIFLLLLDNLRQFRGWTRIDFNIGKLVELGGD
>NZ_CP019636.1|WP_087541357.1|4129923_4130760_-|SAM-dependent-methyltransferase
MSQVVEKAIARPVTPLGILAKQLETILQTFNQQTSNELAANLVLAWRLAAGLDPYLEEHTTHESPALAALAQKTAHEAWGQKFHQGATVRELEQEMLSGHIEGQTLKMFIYMTKAKKVLEVGMFTGYSALAMAEALPPDGELVACEVDPYAAEFAQTAFKESPHGSKIRVELGAAIETLEKLAAAGETFDFVFIDADKREYVQYFQILLDKDLLVPGGFICVDNTLLQGQVYLPSENRTPNGEAIAQFNRIVAADSRVEQVLLPLRDGLTIIRRLPEQ

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Crispr_ID: NZ_CP019636_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_10

4256269-4261825

TypeI-D

I-D,II-B

Consensus_repeat	Method
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CRISPRCasFinder
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CRT
GTTTCAATCCCTAATAGGGAGTAAGAGAAATTTCAAC	PILER-CR

76 spacers

cas2,cas1,cas4,cas6,cas3,csc1gr5,csc2gr7,cas10d,WYL,c2c9_V-U4

The CRISPR arrays of NZ_CP019636_10

>merge|NZ_CP019636|10|4256269-4261825|CRISPRCasFinder,CRT,PILER-CR
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACACTGTTCGGGAGACTGGAAAATACATCATATAAAAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGCCCACGAATTACTCTCGCCGGATGCAGCGCGAGATAGAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGAGATTAAGCTTACAAAAGCTTCATCCTCAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACACGTTTGATTGACTGTGCGAGTGTATCATCTGTGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTCAATGAACTGGTTGTATGGCGGTCGCGCTATTGCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGATGGATTTGACACAGCTATATCGCAATTCCTCGAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATCGTTTCATCAAACGTCCACCGTGGATCATAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGTAGTCCGAATTCTGGTTGCGCAAGATTTGTACTGGGAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGGATAATTATTGCTGATGAAAATCCGGAACTGGTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAAGAGCCTCATATGTCTCTTTGACAAAAGCAAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTTCTGGAGCCACCAGCAGAACATCGTCTCTGGGATGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCAACCACTCTCGATCATGGTGTGCTGCAACTGTTTCAAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAAAGCAGATCCAACAGCAGAAAGTACACCTAGCTGAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGTCGTTCGACTTTGCAGCGCTTAAAAAATATTTCTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGCGTAGCAAGAGCCGTACCAACTCCCACCCCAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTTATCTTGGTAAAACTGTTGGGACAAACTCTAGAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATTTGACCACGGCGGCACTAATTGGTTAACAGGTGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCGGAGCGTTCCCCATCTGGACACAGACGTTTTTAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCTTAAAGTCTTGATGGATATGCCTAACTCTTTGGCAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAAGCAGATCGATACGGGCGTGACTTGGGTGCTAGTTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGAACCATTGAAATACCTCCACTTGCCGAGACTGTGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTGCCTATATTCTTGTAAGAAATCTCTTGCCGTGCGATTTAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTGGAGCGGGATGGCGGTATACACCTTTGTCTGGAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGTGCAAATCTTGCTGAGGCGAGCGAAGAACAAGTTGAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGCTTTATCTCACACGGTCGAAAATGACCTCAAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCGCTAGTGGCAGTAGGCATTATGTATCCACCACTAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGCAGGTTGTCTTGTAGGAAGGAATGCGAGAACTCACTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAACTCGATTCCTCCTCTGTTTTTTGAACTGTAATGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGTCGTCTCCTTCACAGTCGTTGCAATGACTTCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCTGATCTTGCTTGCGAACGCCAAAAACCGCAAAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCTTTACCCAAGAAAGCAAATCTTTGAGGACGTTTTTTAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTTCTCTCCATTTTTTCAGCCTTGCTTCACGAGCTTGTTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTTAAACAATCAGTGCAACCGGATAAGCCAGCCAAGCCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGAGTTGAGGATATTCTCGGAAGGTGATTACCTCAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGACCAGCCGATAACAGTAAATTCCTAGACCAGCAAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGCGCTCAAAATTACCCTCAAAACCTTGCGCAGAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGCTTCATCTGGGCTAACAATGCCGCTATCTTGGAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTGGCGTAATAAAAACGCCCACACCAATATAATAGCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTGTACTTCGCAACCAAACGACAGTAACCTTGGTTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGCTTATCAACATCAGTAAGCAAATTATCAAACTTAGAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGGATATAATGGAAGTAGCTATTTATACATAGCAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCCTATTATCTTAGAAACTTTAGTTGCCAATAATTATGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTAACTCTCTGAATACCTGGTACTTTTTCAGGTACTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCTTGTGTGTTGCTTGGTTGTTCTGTGCTATGGCCAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATATCATAAGTGAACACGCTAACAGTCTTATCAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGAATTAGACAGACAGACAATCGACCAGACTCTAGCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAATCTTCCACGGTTTAACCCTGGTAAAATTCCATAATGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTCGTCCATGCAGTCGATGAAGGAATAATGTCCGGTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAATAGCCTTAATTCCCTCTAAATATTGATACTCGGCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATCTTTATTCAATTGATTAAAACCTGTAGCGTCTTCAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGTCTGACTCATTAACCTTGTTTACAGTCTCTTCTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTCCTTTGTGCTCGCTTATTGGATCTATCCTCTTGTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTGAAACTATCTAACGCTTATTTGGATCGCTCCAGTGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTAATTTACAGACACACAAGTTAGCATTAGAAAGATGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATAACTGGATTCTTCAAGAATTAACCAAGGATGATAAGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAAAGACTTACCAAAAACTAACTTGGCTTGCTCCAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTCTTCAGTTGGTTTGTTGTATCCATCTTTAATCTTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCAGTTGGCAAAGCGTTAGCGTCGTCGTCTTCATCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAGCTTCATCCTGTGACAGTTCCCAATATGGGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTAACTCTTTGATTTACTCCGTGATTTCTTGATTGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTTGACGGATGAAAGCGTACAGCCGGATAGCAGCTGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATACAGTAAAAGAAGTTTCGACGGATAGGACACATGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTGCATCTTCAATGTATGCAATATTAAATTTATTTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATGACTTTGCTCCTCTTTCTGGGTTTTAACCAGCATCATGTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATATCGACGTACTGTTTGCCACACCACACCAACAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTTGGAAGGTTTCATAGTTTCGAGTTGCAATACCGGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACATTAACCTATAAGCGATGTGGTCTGTTGAGTTGTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCTACTTTAAGCAGTTTCGACGTGGCGCCAAAGTTTGTGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACAACAACCTAGCAAACGAGTTTATGGGCGCAAACGCTCAAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCTTTATGGTGAGGGTAGCATTACCAAGCGTAGTGTGTTGGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACACGGTTGGTTCTTCCTTTCGGGTGGTCAGTGGAAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGCTGTAAACTCTATGTGACTATATTAACTGATGTAGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTTGTATTTAATGCGTATACTCAGATACTCAGTAAGGGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACTAGACGCAAACACACTACAACCCGCGCTATACTTTCCGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACCTGAAAGTTGGCACATCTATATTTGAAGCATTTAATGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAACGGAAACAAGCACAACCTCAAAGTGGTGGCGGAGGGTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC

>NZ_CP019636|10|10|4256269-4261825|CRISPRCasFinder
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACTGTTCGGGAGACTGGAAAATACATCATATAAAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCCCACGAATTACTCTCGCCGGATGCAGCGCGAGATAGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGAGATTAAGCTTACAAAAGCTTCATCCTCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACGTTTGATTGACTGTGCGAGTGTATCATCTGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCAATGAACTGGTTGTATGGCGGTCGCGCTATTGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGATGGATTTGACACAGCTATATCGCAATTCCTCGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATCGTTTCATCAAACGTCCACCGTGGATCATAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTAGTCCGAATTCTGGTTGCGCAAGATTTGTACTGGGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGATAATTATTGCTGATGAAAATCCGGAACTGGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAGAGCCTCATATGTCTCTTTGACAAAAGCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTCTGGAGCCACCAGCAGAACATCGTCTCTGGGAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CAACCACTCTCGATCATGGTGTGCTGCAACTGTTTCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAAGCAGATCCAACAGCAGAAAGTACACCTAGCTGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTCGTTCGACTTTGCAGCGCTTAAAAAATATTTCT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCGTAGCAAGAGCCGTACCAACTCCCACCCCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTATCTTGGTAAAACTGTTGGGACAAACTCTAGAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATTTGACCACGGCGGCACTAATTGGTTAACAGGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CGGAGCGTTCCCCATCTGGACACAGACGTTTTTA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTAAAGTCTTGATGGATATGCCTAACTCTTTGGCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAGCAGATCGATACGGGCGTGACTTGGGTGCTAGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGAACCATTGAAATACCTCCACTTGCCGAGACTGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGCCTATATTCTTGTAAGAAATCTCTTGCCGTGCGATTTA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGGAGCGGGATGGCGGTATACACCTTTGTCTGGAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGTGCAAATCTTGCTGAGGCGAGCGAAGAACAAGTTGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTTATCTCACACGGTCGAAAATGACCTCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CGCTAGTGGCAGTAGGCATTATGTATCCACCACTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCAGGTTGTCTTGTAGGAAGGAATGCGAGAACTCACT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AACTCGATTCCTCCTCTGTTTTTTGAACTGTAAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGTCGTCTCCTTCACAGTCGTTGCAATGACTTC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTGATCTTGCTTGCGAACGCCAAAAACCGCAAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTTACCCAAGAAAGCAAATCTTTGAGGACGTTTTTTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTCTCTCCATTTTTTCAGCCTTGCTTCACGAGCTTGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTAAACAATCAGTGCAACCGGATAAGCCAGCCAAGCC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GAGTTGAGGATATTCTCGGAAGGTGATTACCTCA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGACCAGCCGATAACAGTAAATTCCTAGACCAGCAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCGCTCAAAATTACCCTCAAAACCTTGCGCAGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTCATCTGGGCTAACAATGCCGCTATCTTGGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGGCGTAATAAAAACGCCCACACCAATATAATAGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGTACTTCGCAACCAAACGACAGTAACCTTGGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTATCAACATCAGTAAGCAAATTATCAAACTTAGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGATATAATGGAAGTAGCTATTTATACATAGCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CCTATTATCTTAGAAACTTTAGTTGCCAATAATTAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAACTCTCTGAATACCTGGTACTTTTTCAGGTACT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTGTGTGTTGCTTGGTTGTTCTGTGCTATGGCCA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATATCATAAGTGAACACGCTAACAGTCTTATCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GAATTAGACAGACAGACAATCGACCAGACTCTAGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AATCTTCCACGGTTTAACCCTGGTAAAATTCCATAAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCGTCCATGCAGTCGATGAAGGAATAATGTCCGGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AATAGCCTTAATTCCCTCTAAATATTGATACTCGGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATCTTTATTCAATTGATTAAAACCTGTAGCGTCTTCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTCTGACTCATTAACCTTGTTTACAGTCTCTTCT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCCTTTGTGCTCGCTTATTGGATCTATCCTCTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGAAACTATCTAACGCTTATTTGGATCGCTCCAGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAATTTACAGACACACAAGTTAGCATTAGAAAGAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATAACTGGATTCTTCAAGAATTAACCAAGGATGATAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAAGACTTACCAAAAACTAACTTGGCTTGCTCCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCTTCAGTTGGTTTGTTGTATCCATCTTTAATCTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CAGTTGGCAAAGCGTTAGCGTCGTCGTCTTCATC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCTTCATCCTGTGACAGTTCCCAATATGGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAACTCTTTGATTTACTCCGTGATTTCTTGATTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGACGGATGAAAGCGTACAGCCGGATAGCAGCTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATACAGTAAAAGAAGTTTCGACGGATAGGACACATG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGCATCTTCAATGTATGCAATATTAAATTTATTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATGACTTTGCTCCTCTTTCTGGGTTTTAACCAGCATCATGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATATCGACGTACTGTTTGCCACACCACACCAACAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGGAAGGTTTCATAGTTTCGAGTTGCAATACCGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATTAACCTATAAGCGATGTGGTCTGTTGAGTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTACTTTAAGCAGTTTCGACGTGGCGCCAAAGTTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AACAACCTAGCAAACGAGTTTATGGGCGCAAACGCTCAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTTATGGTGAGGGTAGCATTACCAAGCGTAGTGTGTTGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACGGTTGGTTCTTCCTTTCGGGTGGTCAGTGGAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTGTAAACTCTATGTGACTATATTAACTGATGTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGTATTTAATGCGTATACTCAGATACTCAGTAAGGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAGACGCAAACACACTACAACCCGCGCTATACTTTCC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTGAAAGTTGGCACATCTATATTTGAAGCATTTAATG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGAAACAAGCACAACCTCAAAGTGGTGGCGGAGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC

>NZ_CP019636|10|2|4256269-4261825|CRT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACTGTTCGGGAGACTGGAAAATACATCATATAAAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCCCACGAATTACTCTCGCCGGATGCAGCGCGAGATAGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGAGATTAAGCTTACAAAAGCTTCATCCTCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACGTTTGATTGACTGTGCGAGTGTATCATCTGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCAATGAACTGGTTGTATGGCGGTCGCGCTATTGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGATGGATTTGACACAGCTATATCGCAATTCCTCGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATCGTTTCATCAAACGTCCACCGTGGATCATAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTAGTCCGAATTCTGGTTGCGCAAGATTTGTACTGGGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGATAATTATTGCTGATGAAAATCCGGAACTGGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAGAGCCTCATATGTCTCTTTGACAAAAGCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTCTGGAGCCACCAGCAGAACATCGTCTCTGGGAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CAACCACTCTCGATCATGGTGTGCTGCAACTGTTTCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAAGCAGATCCAACAGCAGAAAGTACACCTAGCTGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTCGTTCGACTTTGCAGCGCTTAAAAAATATTTCT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCGTAGCAAGAGCCGTACCAACTCCCACCCCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTATCTTGGTAAAACTGTTGGGACAAACTCTAGAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATTTGACCACGGCGGCACTAATTGGTTAACAGGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CGGAGCGTTCCCCATCTGGACACAGACGTTTTTA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTAAAGTCTTGATGGATATGCCTAACTCTTTGGCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAGCAGATCGATACGGGCGTGACTTGGGTGCTAGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGAACCATTGAAATACCTCCACTTGCCGAGACTGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGCCTATATTCTTGTAAGAAATCTCTTGCCGTGCGATTTA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGGAGCGGGATGGCGGTATACACCTTTGTCTGGAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGTGCAAATCTTGCTGAGGCGAGCGAAGAACAAGTTGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTTATCTCACACGGTCGAAAATGACCTCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CGCTAGTGGCAGTAGGCATTATGTATCCACCACTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCAGGTTGTCTTGTAGGAAGGAATGCGAGAACTCACT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AACTCGATTCCTCCTCTGTTTTTTGAACTGTAAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGTCGTCTCCTTCACAGTCGTTGCAATGACTTC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTGATCTTGCTTGCGAACGCCAAAAACCGCAAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTTACCCAAGAAAGCAAATCTTTGAGGACGTTTTTTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTCTCTCCATTTTTTCAGCCTTGCTTCACGAGCTTGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTAAACAATCAGTGCAACCGGATAAGCCAGCCAAGCC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GAGTTGAGGATATTCTCGGAAGGTGATTACCTCA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGACCAGCCGATAACAGTAAATTCCTAGACCAGCAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCGCTCAAAATTACCCTCAAAACCTTGCGCAGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTCATCTGGGCTAACAATGCCGCTATCTTGGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGGCGTAATAAAAACGCCCACACCAATATAATAGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGTACTTCGCAACCAAACGACAGTAACCTTGGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTATCAACATCAGTAAGCAAATTATCAAACTTAGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGATATAATGGAAGTAGCTATTTATACATAGCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CCTATTATCTTAGAAACTTTAGTTGCCAATAATTAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAACTCTCTGAATACCTGGTACTTTTTCAGGTACT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTGTGTGTTGCTTGGTTGTTCTGTGCTATGGCCA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATATCATAAGTGAACACGCTAACAGTCTTATCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GAATTAGACAGACAGACAATCGACCAGACTCTAGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AATCTTCCACGGTTTAACCCTGGTAAAATTCCATAAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCGTCCATGCAGTCGATGAAGGAATAATGTCCGGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AATAGCCTTAATTCCCTCTAAATATTGATACTCGGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATCTTTATTCAATTGATTAAAACCTGTAGCGTCTTCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTCTGACTCATTAACCTTGTTTACAGTCTCTTCT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCCTTTGTGCTCGCTTATTGGATCTATCCTCTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGAAACTATCTAACGCTTATTTGGATCGCTCCAGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAATTTACAGACACACAAGTTAGCATTAGAAAGAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATAACTGGATTCTTCAAGAATTAACCAAGGATGATAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAAGACTTACCAAAAACTAACTTGGCTTGCTCCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCTTCAGTTGGTTTGTTGTATCCATCTTTAATCTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CAGTTGGCAAAGCGTTAGCGTCGTCGTCTTCATC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCTTCATCCTGTGACAGTTCCCAATATGGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAACTCTTTGATTTACTCCGTGATTTCTTGATTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGACGGATGAAAGCGTACAGCCGGATAGCAGCTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATACAGTAAAAGAAGTTTCGACGGATAGGACACATG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGCATCTTCAATGTATGCAATATTAAATTTATTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATGACTTTGCTCCTCTTTCTGGGTTTTAACCAGCATCATGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATATCGACGTACTGTTTGCCACACCACACCAACAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGGAAGGTTTCATAGTTTCGAGTTGCAATACCGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATTAACCTATAAGCGATGTGGTCTGTTGAGTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTACTTTAAGCAGTTTCGACGTGGCGCCAAAGTTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AACAACCTAGCAAACGAGTTTATGGGCGCAAACGCTCAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTTATGGTGAGGGTAGCATTACCAAGCGTAGTGTGTTGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACGGTTGGTTCTTCCTTTCGGGTGGTCAGTGGAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTGTAAACTCTATGTGACTATATTAACTGATGTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGTATTTAATGCGTATACTCAGATACTCAGTAAGGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAGACGCAAACACACTACAACCCGCGCTATACTTTCC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTGAAAGTTGGCACATCTATATTTGAAGCATTTAATG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGAAACAAGCACAACCTCAAAGTGGTGGCGGAGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC

>NZ_CP019636|10|2|4256488-4261825|PILER-CR
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACGTTTGATTGACTGTGCGAGTGTATCATCTGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCAATGAACTGGTTGTATGGCGGTCGCGCTATTGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGATGGATTTGACACAGCTATATCGCAATTCCTCGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATCGTTTCATCAAACGTCCACCGTGGATCATAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTAGTCCGAATTCTGGTTGCGCAAGATTTGTACTGGGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGATAATTATTGCTGATGAAAATCCGGAACTGGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAGAGCCTCATATGTCTCTTTGACAAAAGCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTCTGGAGCCACCAGCAGAACATCGTCTCTGGGAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CAACCACTCTCGATCATGGTGTGCTGCAACTGTTTCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAAGCAGATCCAACAGCAGAAAGTACACCTAGCTGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTCGTTCGACTTTGCAGCGCTTAAAAAATATTTCT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCGTAGCAAGAGCCGTACCAACTCCCACCCCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTATCTTGGTAAAACTGTTGGGACAAACTCTAGAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATTTGACCACGGCGGCACTAATTGGTTAACAGGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CGGAGCGTTCCCCATCTGGACACAGACGTTTTTA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTAAAGTCTTGATGGATATGCCTAACTCTTTGGCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAGCAGATCGATACGGGCGTGACTTGGGTGCTAGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGAACCATTGAAATACCTCCACTTGCCGAGACTGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGCCTATATTCTTGTAAGAAATCTCTTGCCGTGCGATTTA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGGAGCGGGATGGCGGTATACACCTTTGTCTGGAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGTGCAAATCTTGCTGAGGCGAGCGAAGAACAAGTTGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTTATCTCACACGGTCGAAAATGACCTCAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CGCTAGTGGCAGTAGGCATTATGTATCCACCACTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCAGGTTGTCTTGTAGGAAGGAATGCGAGAACTCACT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AACTCGATTCCTCCTCTGTTTTTTGAACTGTAAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGTCGTCTCCTTCACAGTCGTTGCAATGACTTC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTGATCTTGCTTGCGAACGCCAAAAACCGCAAAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTTACCCAAGAAAGCAAATCTTTGAGGACGTTTTTTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTCTCTCCATTTTTTCAGCCTTGCTTCACGAGCTTGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTAAACAATCAGTGCAACCGGATAAGCCAGCCAAGCC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GAGTTGAGGATATTCTCGGAAGGTGATTACCTCA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGACCAGCCGATAACAGTAAATTCCTAGACCAGCAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCGCTCAAAATTACCCTCAAAACCTTGCGCAGAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTCATCTGGGCTAACAATGCCGCTATCTTGGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGGCGTAATAAAAACGCCCACACCAATATAATAGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGTACTTCGCAACCAAACGACAGTAACCTTGGTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTTATCAACATCAGTAAGCAAATTATCAAACTTAGA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGATATAATGGAAGTAGCTATTTATACATAGCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CCTATTATCTTAGAAACTTTAGTTGCCAATAATTAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAACTCTCTGAATACCTGGTACTTTTTCAGGTACT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTGTGTGTTGCTTGGTTGTTCTGTGCTATGGCCA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATATCATAAGTGAACACGCTAACAGTCTTATCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GAATTAGACAGACAGACAATCGACCAGACTCTAGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AATCTTCCACGGTTTAACCCTGGTAAAATTCCATAAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCGTCCATGCAGTCGATGAAGGAATAATGTCCGGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AATAGCCTTAATTCCCTCTAAATATTGATACTCGGC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATCTTTATTCAATTGATTAAAACCTGTAGCGTCTTCAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GTCTGACTCATTAACCTTGTTTACAGTCTCTTCT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCCTTTGTGCTCGCTTATTGGATCTATCCTCTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGAAACTATCTAACGCTTATTTGGATCGCTCCAGTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAATTTACAGACACACAAGTTAGCATTAGAAAGAT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATAACTGGATTCTTCAAGAATTAACCAAGGATGATAA
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AAAGACTTACCAAAAACTAACTTGGCTTGCTCCAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TCTTCAGTTGGTTTGTTGTATCCATCTTTAATCTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CAGTTGGCAAAGCGTTAGCGTCGTCGTCTTCATC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AGCTTCATCCTGTGACAGTTCCCAATATGGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAACTCTTTGATTTACTCCGTGATTTCTTGATTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGACGGATGAAAGCGTACAGCCGGATAGCAGCTG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATACAGTAAAAGAAGTTTCGACGGATAGGACACATG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TGCATCTTCAATGTATGCAATATTAAATTTATTT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATGACTTTGCTCCTCTTTCTGGGTTTTAACCAGCATCATGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATATCGACGTACTGTTTGCCACACCACACCAACAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGGAAGGTTTCATAGTTTCGAGTTGCAATACCGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ATTAACCTATAAGCGATGTGGTCTGTTGAGTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTACTTTAAGCAGTTTCGACGTGGCGCCAAAGTTTGT
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	AACAACCTAGCAAACGAGTTTATGGGCGCAAACGCTCAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTTTATGGTGAGGGTAGCATTACCAAGCGTAGTGTGTTGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	ACGGTTGGTTCTTCCTTTCGGGTGGTCAGTGGAAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GCTGTAAACTCTATGTGACTATATTAACTGATGTAG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TTGTATTTAATGCGTATACTCAGATACTCAGTAAGGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	TAGACGCAAACACACTACAACCCGCGCTATACTTTCC
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	CTGAAAGTTGGCACATCTATATTTGAAGCATTTAATG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC	GGAAACAAGCACAACCTCAAAGTGGTGGCGGAGG
GTTGAAATTTCTCTTACTCCCTATTAGGGATTGAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087541439.1\|4243832_4244951_+\|DUF2855-family-protein	unknown	unknown	gnl\|CDD\|378541
NZ_CP019636.1\|WP_087541452.1\|4264606_4265920_+\|transposase	c2c9_V-U4	-	gnl\|CDD\|223747
NZ_CP019636.1\|WP_087541445.1\|4254094_4254688_+\|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl\|CDD\|273040
NZ_CP019636.1\|WP_087541459.1\|4274011_4276993_-\|NHLP-bacteriocin-export-ABC-transporter-permease/ATPase-subunit	unknown	unknown	gnl\|CDD\|274789
NZ_CP019636.1\|WP_087541440.1\|4245310_4246174_-\|transcriptional-regulator	WYL	pfam13280_WYL_CAS-I:CAS-III	gnl\|CDD\|225253
NZ_CP019636.1\|WP_087541453.1\|4265973_4267683_-\|iron-uptake-porin	unknown	unknown	gnl\|CDD\|335962
NZ_CP019636.1\|WP_087541455.1\|4270091_4271474_-\|diaminopimelate-decarboxylase	unknown	unknown	gnl\|CDD\|143508
NZ_CP019636.1\|WP_087541441.1\|4246455_4249146_+\|CRISPR-associated-protein-Csc3	cas10d	mkCas0201_cas10d_CAS-I-D	gnl\|CDD\|187843
NZ_CP019636.1\|WP_087541447.1\|4255768_4256056_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP019636.1\|WP_087546237.1\|4253232_4254102_+\|CRISPR-associated-endoribonuclease-Cas6	cas6	COG5551_cas6_CAS-III	gnl\|CDD\|227838
NZ_CP019636.1\|WP_087541454.1\|4267908_4270062_-\|peptidoglycan-DD-metalloendopeptidase-family-protein	unknown	unknown	gnl\|CDD\|377010
NZ_CP019636.1\|WP_087541450.1\|4262490_4263696_-\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951
NZ_CP019636.1\|WP_087541457.1\|4272517_4273012_-\|PqqD-family-protein	unknown	unknown	gnl\|CDD\|377508
NZ_CP019636.1\|WP_087541446.1\|4254741_4255746_+\|type-I-D-CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|274976
NZ_CP019636.1\|WP_087541460.1\|4277042_4279241_-\|NHLP-family-bacteriocin-export-ABC-transporter-peptidase/permease/ATPase-subunit	unknown	unknown	gnl\|CDD\|274788
NZ_CP019636.1\|WP_087541451.1\|4263978_4264431_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|197366
NZ_CP019636.1\|WP_087541443.1\|4250179_4250941_+\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	csc1gr5	cd09711_csc1gr5_CAS-I-D	gnl\|CDD\|274458
NZ_CP019636.1\|WP_087541444.1\|4250933_4253219_+\|type-I-D-CRISPR-associated-helicase-Cas3'	cas3	cd09710_cas3_CAS-I-D	gnl\|CDD\|187841
NZ_CP019636.1\|WP_087541456.1\|4271477_4272518_-\|carboxylate--amine-ligase	unknown	unknown	gnl\|CDD\|237195
NZ_CP019636.1\|WP_087541442.1\|4249159_4250176_+\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	csc2gr7	cd09709_csc2gr7_CAS-I-D	gnl\|CDD\|375747

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087541439.1\|4243832_4244951_+\|DUF2855-family-protein	gnl\|CDD\|378541	pfam11017, DUF2855, Protein of unknown function (DUF2855). This family of proteins has no known function.	5.03369e-114
NZ_CP019636.1\|WP_087541452.1\|4264606_4265920_+\|transposase	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	6.75332e-34
NZ_CP019636.1\|WP_087541445.1\|4254094_4254688_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	3.15859e-52
NZ_CP019636.1\|WP_087541459.1\|4274011_4276993_-\|NHLP-bacteriocin-export-ABC-transporter-permease/ATPase-subunit	gnl\|CDD\|274789	TIGR03797, ABC_transporter_related, NHLM bacteriocin system ABC transporter, ATP-binding protein. Members of this protein family are ABC transporter ATP-binding subunits, part of a three-gene putative bacteriocin transport operon. The other subunits include another ATP-binding subunit (TIGR03796), which has an N-terminal leader sequence cleavage domain, and an HlyD homolog (TIGR03794). In a number of genomes, members of protein families related to nitrile hydratase alpha subunit or to nif11 have undergone paralogous family expansions, with members possessing a putative bacteriocin cleavage region ending with a classic Gly-Gly motif. Those sets of putative bacteriocins, members of this protein family and its partners TIGR03794 and TIGR03796, and cyclodehydratase/docking scaffold fusion proteins of thiazole/oxazole biosynthesis frequently show correlated species distribution and co-clustering within many of those genomes. [Transport and binding proteins, Amino acids, peptides and amines, Cellular processes, Biosynthesis of natural products].	0
NZ_CP019636.1\|WP_087541440.1\|4245310_4246174_-\|transcriptional-regulator	gnl\|CDD\|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	5.15156e-08
NZ_CP019636.1\|WP_087541453.1\|4265973_4267683_-\|iron-uptake-porin	gnl\|CDD\|335962	pfam04966, OprB, Carbohydrate-selective porin, OprB family.	8.58862e-39
NZ_CP019636.1\|WP_087541455.1\|4270091_4271474_-\|diaminopimelate-decarboxylase	gnl\|CDD\|143508	cd06841, PLPDE_III_MccE_like, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme MccE. This subfamily is composed of uncharacterized proteins with similarity to Escherichia coli MccE, a hypothetical protein that is homologous to eukaryotic ornithine decarboxylase (ODC) and diaminopimelate decarboxylase (DapDC). ODC and DapDC are fold type III PLP-dependent enzymes that contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain, similar to bacterial alanine racemases. ODC participates in the formation of putrescine by catalyzing the decarboxylation of ornithine, the first step in polyamine biosynthesis. DapDC participates in the last step of lysine biosynthesis, the conversion of meso-2,6-diaminoheptanedioate to L-lysine. Most members of this subfamily share the same domain architecture as ODC and DapDC. A few members, including Escherichia coli MccE, contain an additional acetyltransferase domain at the C-terminus.	5.73168e-144
NZ_CP019636.1\|WP_087541441.1\|4246455_4249146_+\|CRISPR-associated-protein-Csc3	gnl\|CDD\|187843	cd09712, Cas10d_I-D, CRISPR/Cas system-associated protein Cas10d. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Large proteins, some contain Zn-finger domain. Fused to N-terminal HD domain; signature gene for I-D subtype; also known as Csc3 family.	0.00245721
NZ_CP019636.1\|WP_087541447.1\|4255768_4256056_+\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	5.59885e-38
NZ_CP019636.1\|WP_087546237.1\|4253232_4254102_+\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|227838	COG5551, COG5551, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.8157e-52
NZ_CP019636.1\|WP_087541454.1\|4267908_4270062_-\|peptidoglycan-DD-metalloendopeptidase-family-protein	gnl\|CDD\|377010	pfam03253, UT, Urea transporter. Members of this family transport urea across membranes. The family includes a bacterial homolog.	4.4384e-41
NZ_CP019636.1\|WP_087541450.1\|4262490_4263696_-\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	1.6339e-62
NZ_CP019636.1\|WP_087541457.1\|4272517_4273012_-\|PqqD-family-protein	gnl\|CDD\|377508	pfam05402, PqqD, Coenzyme PQQ synthesis protein D (PqqD). This family contains several bacterial coenzyme PQQ synthesis protein D (PqqD) sequences. This protein is required for coenzyme pyrrolo-quinoline-quinone (PQQ) biosynthesis.	6.91354e-10
NZ_CP019636.1\|WP_087541446.1\|4254741_4255746_+\|type-I-D-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274976	TIGR04093, hypothetical_protein_L8106_25395, CRISPR-associated endonuclease Cas1, subtype CYANO. 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 a clade of Cas1 limited to the CYANO subtype of CRISPR/Cas system and most often the type found there.	8.97089e-156
NZ_CP019636.1\|WP_087541460.1\|4277042_4279241_-\|NHLP-family-bacteriocin-export-ABC-transporter-peptidase/permease/ATPase-subunit	gnl\|CDD\|274788	TIGR03796, ABC_transporter_related, NHLM bacteriocin system ABC transporter, peptidase/ATP-binding protein. This protein describes a multidomain ABC transporter subunit that is one of three protein families associated with some regularity with a distinctive family of putative bacteriocins. It includes a bacteriocin-processing peptidase domain at the N-terminus. Model TIGR03793 describes a conserved propeptide region for this bacteriocin family, unusual because it shows obvious homology a region of the enzyme nitrile hydratase up to the classic Gly-Gly cleavage motif. This family is therefore predicted to be a subunit of a bacteriocin processing and export system characteristic to this system that we designate NHLM, Nitrile Hydratase Leader Microcin. [Transport and binding proteins, Amino acids, peptides and amines, Cellular processes, Biosynthesis of natural products].	0
NZ_CP019636.1\|WP_087541451.1\|4263978_4264431_+\|hypothetical-protein	gnl\|CDD\|197366	cd09916, CpxP_like, CpxP component of the bacterial Cpx-two-component system and related proteins. This family summarizes bacterial proteins related to CpxP, a periplasmic protein that forms part of a two-component system which acts as a global modulator of cell-envelope stress in gram-negative bacteria. CpxP aids in combating extracytoplasmic protein-mediated toxicity, and may also be involved in the response to alkaline pH. Functioning as a dimer, it inhibits activation of the kinase CpxA, but also plays a vital role in the quality control system of P pili. It has been suggested that CpxP directly interacts with CpxA via its concave polar surface. Another member of this family, Spy, is also a periplasmic protein that may be involved in the response to stress. The homology between CpxP and Spy suggests similar functions. A characteristic 5-residue sequence motif LTXXQ is found repeated twice in many members of this family.	1.62148e-05
NZ_CP019636.1\|WP_087541443.1\|4250179_4250941_+\|type-I-D-CRISPR-associated-protein-Cas5/Csc1	gnl\|CDD\|274458	TIGR03159, cas_Csc1, CRISPR type I-D/CYANO-associated protein Csc1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a widespread family of prokaryotic direct repeats with spacers of unique sequence between consecutive repeats. This protein family is a CRISPR-associated (Cas) family strictly associated with the Cyano subtype of CRISPR/Cas locus, found in several species of Cyanobacteria and several archaeal species. This family is designated Csc1 for CRISPR/Cas Subtype Cyano protein 1, as it is often the first gene upstream of the core cas genes, cas3-cas4-cas1-cas2.	1.14124e-75
NZ_CP019636.1\|WP_087541444.1\|4250933_4253219_+\|type-I-D-CRISPR-associated-helicase-Cas3'	gnl\|CDD\|187841	cd09710, Cas3_I-D, CRISPR/Cas system-associated protein Cas3; Distinct diverged subfamily of Cas3 helicase domain. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Diverged DNA helicase Cas3'; signature gene for Type I and subtype I-D.	2.40054e-127
NZ_CP019636.1\|WP_087541456.1\|4271477_4272518_-\|carboxylate--amine-ligase	gnl\|CDD\|237195	PRK12767, PRK12767, carbamoyl phosphate synthase-like protein; Provisional.	4.2324e-32
NZ_CP019636.1\|WP_087541442.1\|4249159_4250176_+\|type-I-D-CRISPR-associated-protein-Cas7/Csc2	gnl\|CDD\|375747	pfam18320, Csc2, Csc2 Crispr. The Csc2 Crispr family of proteins forms a core RNA recognition motif-like domain, flanked by three peripheral insertion domains: a lid domain, a Zinc-binding domain and a helical domain. The CRISPR-Cas system is possibly a mechanism of defence against invading pathogens and plasmids that functions analogously to the RNA interference (RNAi) systems in eukaryotes.	7.29471e-161

>NZ_CP019636.1|WP_087541447.1|4255768_4256056_+|CRISPR-associated-endonuclease-Cas2
MNVVVSYDISEDKRRTKIHKVLKSYGQWVQYSVFECQLTDTQYAKLRSRLNKLIKPETDSIRFYFLCVCCFGKIERIGGEQPRDETIFFAECADG
>NZ_CP019636.1|WP_087541446.1|4254741_4255746_+|type-I-D-CRISPR-associated-endonuclease-Cas1
MGTVYITQEDAFIGKIDERLTVKFDKKTILDVPLIKIDGVVVLGRATVSPATISELLERQIPLTFLTDTGRYLGRLEPEVTKNIFVRKAQWQAAGESTQAIHVVQGFVRGKLKNYRNFLIRRQRECPGLDLSENVTRLEQAIAPIDKTQNINSLRGLEGAGSAAYFGCFHQLLRTTEFTFTKRVRRPPTDPVNSLLSFGYSLLRHDIQGAVNIAGFDPYLGYLHCDRYGRPSLALDLMEEFRPLVVDAVVLTALNKRFLIPTDFITEPLSGAVSLTSEGRKTFLRLYAQKKQAEFKHPVLGRKCMYQEAFELQARLLAKYFMGEIEKYPPLVLK
>NZ_CP019636.1|WP_087541445.1|4254094_4254688_+|CRISPR-associated-protein-Cas4
MNDTEYIPIAALNQYAYCPHRCWRMFCVGEFIDNQYTIEGTSLHQRVHTVGEGHQQETWQIRAIWLKSDKYQLIGKADLIEAENSDWYPIEYKRGRKGEWDNDELQVCAQALCLEEMTGQRVSSGYIYYAHSHQRQFVEMTEELRQSTIATIEAVQTLLFTGAMPKAVKTRRCTGCSLQLRCLPGTADKVGRYQETE
>NZ_CP019636.1|WP_087546237.1|4253232_4254102_+|CRISPR-associated-endoribonuclease-Cas6
MPHSLVLNLIPQSPIYPEFLTGRHYHALFLTLISSVDRTLGDYLHQSNAEKAFTLSPLQVQRNHKNHQHKHHTLQFCHQRPIPAGTPCWWRISLLDDNLFSKLTPLWLNLNPNHPWHLGSADLYITSIFGTPQSTQPWANACTYAQLYEQASDRTRTLHFIFATPVAFRQGGYDTVLPTRECFFNSLLTRWNKFSGIEFTNAPIESIYPSFCNIHTEVVSNYDSKFIGCVGEISYRILGDIEPVAIKQINTLADFALYAGVGRKTTMGMGMTRRLSITNSRSSNIESHE
>NZ_CP019636.1|WP_087541444.1|4250933_4253219_+|type-I-D-CRISPR-associated-helicase-Cas3'
MGNQKLVTKLEPRSIFACASLPEKLSFMNNALQHQIEVFEKSRDVNIILDLAPTGTGKTKAGFTVLLHKPTKSAVYIAPTNALVEQQREAAEEFVKEAGLPHVVKSASAREIRTWSDDNVGKRPGEKLYNVLRNPATIFPEVGANKPIILVTNPDIFYYATFFAYNKLDRSNIANSFYTKFATVIFDEFHLYDAKQLVGLLFYLAYSHIFGFFKDGRRVVLLTATPEPACELALQSLEKQGVRIAKINGETGNSNLLPSQTAVNLELRPQPDTREEWLAELTSEVVKRFQERPKENGAVILDSLDSINRLKELLDKQGLTDFIGRITGPAPFKDRQRAMQCQIILATSTVDVGFNFERNPAPTRQNLDWLIFSAHNRAAFWQRIGRVGRVLGKSETNIDSEAIAYLPAIAWEQGLASLNISGGRAALEQTLKDVPCLDKPLLIAYWRSEAFLEIARPLLELEEAFQDIPGAELIPQLFETVKSTLGGNRTWDDCRFRMKVLRGAENISKASLKDVQNKWKFTAGGQAFVRTYIKAKYPEDWEDLQAGRVTLDKYESVFKQDEEAAKDLKEFAEIFSTSYAPLFSFRNSLFENLPIRDPHGYLLDESEETRLDPIHLLRHYEFIPNGEFIEVGSRAKDNYELVFRLSYSDTWQEFVNTELNKLTAFKNCRIERRLGVGGAIRPTPLIQVLEKYLIPGMIIAEKENQYIIFQMRKEGIVSYPIVIQCSNAQKEYRFLPGIAGILTMAMKGKQLRLPDDEPFIV
>NZ_CP019636.1|WP_087541443.1|4250179_4250941_+|type-I-D-CRISPR-associated-protein-Cas5/Csc1
MSTIPFQQAKLVELLCLEPIFFASRELSDTYYTEGTIGNYALTYALGLVHSPYRLQGQATGRPTYKEDFQAIAQAFYILPASPINGRVTFRFERFNALSDSYWYAMTNNRVATAREDVPLQRQGKKPNSFRPSNFPQTGRLRMIERGNKFQTVVFGNYELPEYIRVGKFASKVRVNILEKFDVIPLPEGNYQTRAYLNVADLPPQTEILSFDLISMPPAPILKNLHFRGAAWQVGEIIVPEGLQFCCGARLNG
>NZ_CP019636.1|WP_087541442.1|4249159_4250176_+|type-I-D-CRISPR-associated-protein-Cas7/Csc2
MSIQKLSPVLAQTYENFPKGRFISLVVLRKTQSETIFRTEGSGEPICSEFVQAGINDEDIIQRLVMTKRKQVAPERRYGREHLRAHELLYTSKDGSLCSLNTNSPCEMCVDCFLYGFAAGGGGAQKSRIWTEDAFSVLPATEVLGERTINAIYENGTMRDQNGNASTALNTSEYIKPGVHFLDIVTLKDVTADELRYVIGNILYTSRYGAVSSRVGRMENAILGIFGSIAELPSSLELVQAVYDALEKPLEHPMNTKRLTEKAKEVLSSWKNKRGVSVSLSDEELASVMTDVDNHWSAEERDNFLKRLSQSYEPFRQVPAESKKGKSKGKKAPVEVES
>NZ_CP019636.1|WP_087541441.1|4246455_4249146_+|CRISPR-associated-protein-Csc3
MSKRTRLLNRPPKTLEERYFSEIRPLLYERLGTHHQYGVRKGTTLAEHLDSACQFMLTVSRIARVPEDKRPVLLAATAVHDLNKLDPLERKVKTLARDRGFLREQFELAGVLSLVSTEEDFELARRLIERHSGHNVTDGARFLPEDPAIERWAAMITAADLFDLGIPDAERFRKVQNELTVAFDRSSNLFRVRLSEDRGYITALLLGACEEVLTKYGLTALAIFPDGELFEGEAIPKIDLVTEIADVWQRKIDEVFGNNIERLVRPTKDGIKIAHQAIQQNADEVLVNVEALLEKKKAGYKSDKVAKDISKWGDAAGTDAVKNAADLELLPVNNAEEFAVSEGLKAAYLSYREVGLNPKEVWDKIAHYVGISEQQRTVLEAFNGQYGRPLFAAKAAVKGIEGIKEALRESFQLRMKSTQASQATEVSEEMIAVVNRMLNLPIPSKLDGLKELDAYVEANPKLRCSLGSTSNEIKELISDTMPPGTKVQAFSNRLPGGISAEPKRQADSIAALAYQLMTVGANFPAVKKQDPLYLHFALPKGSSPELLRLWREYLERLAATNAEGGTVTVDEFQLYRENSLEFKANKVVGFAFPKRPDFVHTTVIIPLVWGDANASLALLKSLRLALELSLSLEFGFPFTVSGNLEVELSNDIYGRVEGIPASLQPLLGNGQYKRQDSEKILERLRCIGKLATSVASIQKLNDCLYDLARACVRPIELYYVLLRWTLREQDEPNLSITWSRIREPLNTLLENLMPNDNSLLTQYLKEAAQVAAEGKIWGSSFKRTAQAEPFTALITAIRSQKPHLGLDVIFAALIQQYHTRLDRIREHGVGQTKLEQIKRYYEVLRKLYEDVYQARPEKFLADHKTLEAAYLFFLEEARQQLKGKPEENSVEASTSV
>NZ_CP019636.1|WP_087541440.1|4245310_4246174_-|transcriptional-regulator
MPRKKDTITLSIPPGTKEKLEEIARHFDISWGKEPSISGLIVAIAEQTLEVGKPFTLDSNQVNALQRAIKALNDAGCIGEAQTVLALLLERGNLEPPLRQSLMKQISQSTQGWRIQIEDWRKKQQPFYILYRNSQGKELEYTIRHAEPRSFDNRFYLLVWCEETDDVENDIPELPELWHNRTLTYDRIQSAVPINGNWRGQLDYLEVYLHFYSWLKKGYQPKDDDVSDEIIGDVRQVVRRVANPFWLIREVARYWDECVIVSPESMRDRLKHKVRNLCQLYEIETKA
>NZ_CP019636.1|WP_087541439.1|4243832_4244951_+|DUF2855-family-protein
MLTTIRNARDFIVYRKDLSQYQFVSTEIEENLKSGQVLLKVDKFALTANNISYALIGETLGYWDFFRTVEEAWGCIPAWGFAEVVCSKKDNVAKGDRVFGFVPMSTHLMLQPDVVTQEGFVDGSLHRVNFPMLYNQYQLVKHDPFYAPEYEDHWALFWPLFMSAFVLEEFLNENNFFDAQAIVISSASSKTAIALAFLLSRKQSSQCQVIGLTSSGNLSFVEGLGYYNQVLTYDQIQLLNCDLSVVYVDIAGDRDVLSNLHHYFQNMRYSCLLGATHWKRLSSLEINPTLPGPRPTLFFAPEQIHKRVQQWQVNGFHKRFGKLWSQFLASTSEWIQVVHSPGKAAVERIYLDMLAGRPKPDEGQILSLWEVE
>NZ_CP019636.1|WP_087541450.1|4262490_4263696_-|sensor-histidine-kinase
MNRLIQLQYHPFRLLLYLEWILLGIFLLLPPQPPHMPQIHQQPLQSFLITACFGVMGLWLPTSNLFSKVLYIGLGFGLILLAGVMGRGIHVPPPLLLILVIRGCLVFNLIGRLLVAGLAFVCFVFTTLVPLLSKPPLDYVHKPPVVDIWRLVLDVGLMFGLVLAFVLLLVNALLAERQSREKLAIAHQQLSEYALCIEDQATLKERNRIAREIHDALGHSLTAQSIQLENALLFLSSNLDKTKTFLLEAKQLGSNALKEVRQSVATLRCDPLQGKSLESALALLLEDFQRQTGIVPVCSLSLPRSLPTEVGTTIYRIVQEALTNISKHSSATQVKIDLQATSDSLYLQLCDNGKGFNPKQNKTGFGIQGMRERTKALGGQFSIVSSPKGGCQIIARFPYRG
>NZ_CP019636.1|WP_087541451.1|4263978_4264431_+|hypothetical-protein
MKLKSQFIVILAGTISLVVSLHLAKTFAQIPVDNGPIKVVPAGRVPPGPLFPELAGINLTEEQQKQIWQIQQEIMPQIAQIIPHPELTEEQKNQLRSGQSVQITIQPPTAEQKAKLRELFQTYQQRVETILTPEQQQKFRENLKNLPPLS
>NZ_CP019636.1|WP_087541452.1|4264606_4265920_+|transposase
MFNLTYEFKLKPTQNQIVMFEEWLETHRRVSNHALAERKDWYKSRSCQVNACSLHSCYIIPADAPRPTFASQCKFLTAARKENEYLKRVNAQSLQQTLRRLEKAFVSMWEQNHGFPRFKKPGRMRCFSFPQLGVNPLSDGFVKLPVIGAVKMRQSRSIPDGGVIKQARVVKRVSGWYVMLTVQWDVSTPQPMPSGFALAYGGKPSPKFPQRGEPPHGTSLCSAVSPRGEAVGIDVGLTSFVATSNGLLVKRPRFFVDAERKLKFLQQRVSRKRIGSNNWKKAQKKVASLHEYVANCRKDWHRKLSHQICNNAGMVFVEDLNLVGLSRGMLGKHCLDAGFGQFFNILEQTCFKRDVYFQKVDSRKTSQICPSCGVQTGKKELSERTHVCSNCGYTTDRDVAAAQVVAIRGLAAVGHTVKMLAEGKFVGIPVTQESSSL
>NZ_CP019636.1|WP_087541453.1|4265973_4267683_-|iron-uptake-porin
MMSKIVWKNLIINLTSLFGGFLVTNGTLVEAMAHSPGDRSASSTLPFETNAISIPATVPTDSVKSLDSTLSQPEIIQANNFTPTVLDKPSLEMAPMAQINSVFQLSDVTPTDWAFQVVQSLVERYGCISGYLDKTYKGNRSLTRYEFAATLNVCIECINKLLVENTSNLVKKKDLETLKKLQEEFATELTVLRGRVDNLETQTATLQEENFSPTAKLVGEAVFAITDEFNQQSKNSTVFQARVRLDIQNSFTGKDLLHIRLAAGNTNIFNLKGGGVEGIQTFNFGNTNNSIYVDWLSYFFPIDKNTQGYVAAVGGVHYDFVPTVSSYLEGYDSGAGSLSIFGQHNPIYLIGGGSGGGFTYSLSKNLSFSAGYLADNSDLVNGNYAALAQLTFTPNDQFSIGLTYINAYRKFAIFDTGSNLASVGTNLANGGGFDFGTVPSKVNAYGVEFTYKFSPQFAINGWFSYINAEFVKLGTGDIWTYALTFAFPDLGKKNNLGGIVVGVEPYLGNASEFALDAKNDIPIHIEAFYKYQLNNNISITPGVIWILSPGQNSENPDAIIGTIRTTFLF
>NZ_CP019636.1|WP_087541454.1|4267908_4270062_-|peptidoglycan-DD-metalloendopeptidase-family-protein
MWNVLYQSALGRFKLTSSNNQKQRTQGWATMQWLQTLRRLVPAVCAATAEILFLRGSTIGALLLAAMLLQPSVLIMGLFGVLAAVIFTRVTQVATYLVQGPLLFNPLLAGLSVGYLFRPSAASFFLAAAAGILAFVLTWTLSHVLYTFFLLPVLSLPFVAVSWSIHLAAFRFAGLQHAVVPAHAYSIGLPIPLEGFLRTLGLIFFLPNVWVGMAVALLLLLNSRIQFLLAVFSYTFGVFIQGILTGTFAYVYYDPAALNFILVGLALGGYYLLPSPQSYIIAAIGVALAALLGQAVSVFWAAVALPVHAFPYNLVTLLLLYLLGLVGHQLLARYPQSSPEKTLDYELTARRRYQGSSGRLLTLPFAGCWVVWQGFDGQWTHQGLWRYAYDFVIQDEQGLTYRDSGLQLTDYYAFQKPVLSPIRGWVVQVVHDLPDCEIGKVDQEHNWGNHVILYNERGFYVEISHFAQNSIVVKPGDRIEPGALLGRCGNSGYSPQPHIHIQVQLTPVLGAATVPFNFANLIVNGEFCGEGTPGVNAVLEPATPERELAQAFSLPLDSQLHFSITQKGRAIGQLAVIVRMAADGSFYLDSGKAKLFYSRDENRFIFHRLDGEDPWLALLFLAIPRLPLARQAGQQWFDYLPISMVVSGVRLLAYQFCSSFYPRLASARYVGRWQSDKTLIGTISIPKVACKICTFAFFNDENQLVGVNVGDLSLVRL
>NZ_CP019636.1|WP_087541455.1|4270091_4271474_-|diaminopimelate-decarboxylase
MLTQYERPVIQKLHSGLMNKFAGNTLLHRKVKTEIADVPIDDLVAQFGSPLFVYSEQTLRRKFRTIRNAFTTRYPDVTFGWSYKTNYLKAICAILHQEGAIAELVSKMEYDKAKALGIPGNQIILNGPHKPFAMLEAAVRDGVIINIDHLDEIEDLEAIATRLNRIISVGIRLNLDAGIQPCWSRFGFNLESGQAMNAIERIASGGKLRVNGVHSHIGTFIMEPAAYARQVKKMVAFGYEVEQKYGWRMDYIDIGGGFPSRSRLKGMYHAVEVMLPSIEEYADAICDALWASLKPEHTPKLIIESGRAIIDEAGTLITRVCGTKQLPDGTRAYVIDAGVNLLFTSFWYRFDIALGHPVSGRCEPSVIYGPLCMNIDVVDDRISLPPLSRGDRLVISTVGAYNNTQWLQFIEYRPNVVLVTQTGDVELIRAAEDLSDLERREHLPPRLAVVSVPNNPMIKL
>NZ_CP019636.1|WP_087541456.1|4271477_4272518_-|carboxylate--amine-ligase
MKPFTIAITGINAVDNPGPGTGIARSLREDNQLPTQLIGLAYDAMEPGLYMDWLFDRRYLMPYPSSEPEVLIERLQQIQQQVGLDCVIPNLDVELPLYIRCAKELESLGIQTYLPTREQFALRNKARLTEVADAFGVQTPPTLTVNSSQELHEAIASLKLPLIIKGPYHRAYWVLTEQEALQRFHQLATECGYPIIVQKIVSGTEVNLVGIGDGEGSHLGLVATKKMLVTELGKIWSGVTIHHPGLLQVADAFLQHTRWKGPFELECIADFNGKIHLIEINPRFPAWTYFATGVGVNLPARLVRAALGLPLPSVSSYEAGKLFMRYTYEMVTDATPLQTLVTLGEL
>NZ_CP019636.1|WP_087541457.1|4272517_4273012_-|PqqD-family-protein
MSSYDRQLLCPTKGTQSTHETDIRSERKTQAPLRIAASPATPTSSSVNFVAQIFDLGGQPNLIATDILSSTSFCNITNITKERMPVFESLTVTKDGFAFDFATGESFMLNHCGQLVLQRLRHGETQQQIVQFLCSRFDIQQSIAERDIADFCQQLNALGLTEDN
>NZ_CP019636.1|WP_087541459.1|4274011_4276993_-|NHLP-bacteriocin-export-ABC-transporter-permease/ATPase-subunit
MKINETLLLDNPETLWVVQSGKLALFATTVKDGSVAGHRRYLFSVNTNEALFGTLPLGDGRIALQPELRSGCLQASLGGTHEVSRAPDPLRDRIVSGKWVFQAVAVEPTKLIQLPMSELEQRIAASEPEAITLVENWVYNLGQAVKQQQTVLAMPLNLNQTKFERSFSLSPSEELQIRQKEVFWVKFQQGNACWLGIKELTLNSASPVCPLTAGIWLEAEDTSVGTMLSTVELEPDQLQAGLASLHTYLFFYFSLLLNQEAEAEHRRFQEREQLNRQVAAGALGELAAVLQPQQEAVFFQEGPPLLVAMGAIGRVLGITIHPAADDLHNTKDPVTAIACASQIRTRRITLADDWWHREHGPLLAFTQWEKRPVALLPIRGKGYELFDPTSQTRTFVTKSVSKTLSPQAYVIYRPLPQVINNAIDLLRFGTKGIEKDIASIFFLGIIGTLLGMITPQATAILVNQAIPDSDRSSLWQIGLVLLAMAFAQLAFSIAQSIVTLRVQSLTDSTLQPALWDRLLRLSPAFFRQYTSGDLVRRVMSVKAIQQKLNGATQRTLLSGIFALFNLILMFAYSWQLALVGMGLGLLASIITLISSFFLVKKSRQQQEVDGAIYGLTIQLINGVTKLRVAMAEERAFAAWAKKYTQRIRLKASVQQIVDLVSVFNEALPLVSSAMVFGFAITTIQTSLTQTSLTIGTFVAFNYALGIFIKGVIDLSNTITDIWSIIPLWERTQPILRSQPESDTHKEHPGTLIGRIRLNHVSFRYSEDGPLILNDISLNAEPGEFIAIVGPSGSGKSTILRLLLGFETPTIGSVFYDGHDLARLDLQALRKSLGAVLQNGKIGSGSIFENITGGALVTLEEVWEAARMAGLADDIEQMPMGMHTIISEGGGNLSGGQRQRLLIARSLVCKPKVILMDEATSALDNRTQAIVSASLDQLQATRVVIAHRLSTICNADRIYVIDAGRVVQVGTFSQLISQEGLFARLVARQSILFD
>NZ_CP019636.1|WP_087541460.1|4277042_4279241_-|NHLP-family-bacteriocin-export-ABC-transporter-peptidase/permease/ATPase-subunit
MLFPLISNLSHYMKIRRVRTPTVLQMEAVECGAASLGIILSYYGCIVPLAKLREECGVSRDGSKAFNILKAAQNYGLNAKGLKVPLEKLKAIHLPYIVFWNFNHFLVVEGFGNKRVYLNDPASGRRSVSLDEFDQGYTGVVLRMEPGSNFQKGGKKSHIISALTARLKNSWGTILFCLFAGLLLTIPRLAVPAFSQVFVDEILVQNRQEWLRPLLLGMIITGILRALLARLRLTYLRRLMVKLSVSMSGQFLWHTLRLPVGFYDQRYAGEISSRVQINDSVAEILSGRLATTVIDSVMMVLYLIIMIQYNLVLSAIAVSFAAINIIALQLLSQARVDTNLRLVQEYGKVSGVTVAGIQTIETVKASGLEADLFSRFAGYYANVLNTQQELGLQTQILTTLPTFLTALATASILVVGGLEVMNGKLSIGMLVAYQSLTQSFLEPVNSLVNFGSTLQELEADLNRLDDVLQNPIDSEAKREAGKEIISFSLPKLQGYVELRNVTFGYSRLEPPLIENLSLTIQPGQRVAFVGKSGSGKSTIAKLICGLYEPWDGEIYFDGIPRKQIPRSVLANSLAMVEQDIFLFAGTVRDNITLWDQTVPAADLVQACQDAAINDLILSMPKQYDAELIEAGMNISGGQRQRLEIARALVKNPAVLVLDEATSALDAETELIIDQNLRRRGCSCIVVAHRLSTIRDSHEIIVVEGGKIVQRGSHEELWRQGGTYICLIKTEEA

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Crispr_ID: NZ_CP019636_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_11

4554512-4557231

Orphan

I-D,II-B

Consensus_repeat	Method
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CRISPRCasFinder
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CRT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	PILER-CR

37 spacers

The CRISPR arrays of NZ_CP019636_11

>merge|NZ_CP019636|11|4554512-4557231|CRISPRCasFinder,CRT,PILER-CR
ATTTTAATCTCTAATAGGGATTCGTATCAGTTGTAACTTTAGACCCATTTAGTGACAAATCAAACTGGAGCGAATATGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTTTGCTTGAATGAGCGCTCTTATCTTGTTGCACGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTTGTTGTCCTTCGTTTCATAATAGAAAATGGTGGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACGCAGGTTGGATTTCAGCATCTCAAGACTGGAGCCTTGATGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACCCTTGAAGAAGGCATTCGATGCTAAACTCATGATGTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTGTCTGGACATTCTCTGGTGAGATGTTCAGTCGTCGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACCTCTCTCTCCCAGTCAGCGCTGACAATAAAAGCTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACGCTAGCCCATTTTAGCCAACACCCAAGAAACTAAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTCAACTTGGGGTTTCTGTATATGCGCCAAAGTACATACGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACGAGAAGGTGTTGAATGGTTTGTAAGAAACAGTCGTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACCTGCTAAGGAATTACTGAAGAGCATAGACCCACAAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTACTCTTCGATGCGTTTTTCTGAGAGAATAGTGGGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTCTGAAGTACTTCAGAAATAAATAATCATAATAAAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTTTGTTCGTCTAACGTAAATGCTGAGTCTTCTTTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACGGATATGTTGTGGAGCCGTATGTGGTTGCAGTATGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACAAAATACTGGGAGTACGTAAGAGCATTGCTGTGTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACGACAGAGGAGGAATCTTGGAAATTACGAGCTTTACGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACAACTACCGCTGTGAGCGCTCAAAACGACTTGCAAGCCATGAAAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACATGGCTTAATTTTAGCCTACAAGCTGCTTGAAACTTACAAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTGAGACGCTTGGGGATGCCAGCCGTCACTTCAGGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTCAGGCATAGCTTACCTAGCTAAAATAACTCTTCTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACATGTTCCACAGTGCAGAAGCGGATGAAACGATGTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACATCCCGATTATCACGGGAGTATCCTTACCAGATAGGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTATGACCACTACGGTAAGTATATTTGCGGTGCGGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACCTCTGTTGTTCTCACAACGATAATTACTAACAAAAACTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTTATGCCTCAAACCTTTCTCAAGTCATCAAACAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACGTACTATCTAGACTGGCGCGAGAAAGTCTAAGACTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACACGTGCTTTCTAAACTTGCAGTGACCGCACCATGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACACTTTACGTGCGTTAGCAACAGACGTAGACAAATCGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTAAATCTCAGCAACAAACAGATTGAGGAAATTGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTTAATAGAGAAAGACGAAGTCTATTATGATTGGCATGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACAACTCAATAGGTTTGAACAAGCAGAAAATATTATAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACAAATCTTGGTTTTTACAAGTTCAGTGGAATGATTCAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTCAATACCTTGCTCATACGTTATCCTAACCGGATATGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTCTAGACGACTTCTGAGAAGGCTCTCTGGCAGAGGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACCGGGTGGTACGCGAGCAGCAGGTGGACCAATTGCGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAACTGCAAAACAGTCACGTCACAAAGAGCGATCGCGGACTTAGTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC

>NZ_CP019636|11|11|4554512-4557231|CRISPRCasFinder
ATTTTAATCTCTAATAGGGATTCGTATCAGTTGTAAC	TTTAGACCCATTTAGTGACAAATCAAACTGGAGCGAATAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTTGCTTGAATGAGCGCTCTTATCTTGTTGCAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTGTTGTCCTTCGTTTCATAATAGAAAATGGTG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GCAGGTTGGATTTCAGCATCTCAAGACTGGAGCCTTGAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CCTTGAAGAAGGCATTCGATGCTAAACTCATGATGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTGTCTGGACATTCTCTGGTGAGATGTTCAGTCGTC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTCTCTCTCCCAGTCAGCGCTGACAATAAAAGCT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GCTAGCCCATTTTAGCCAACACCCAAGAAACTAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAACTTGGGGTTTCTGTATATGCGCCAAAGTACATAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GAGAAGGTGTTGAATGGTTTGTAAGAAACAGTCGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTGCTAAGGAATTACTGAAGAGCATAGACCCACAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TACTCTTCGATGCGTTTTTCTGAGAGAATAGTGG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCTGAAGTACTTCAGAAATAAATAATCATAATAAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTTGTTCGTCTAACGTAAATGCTGAGTCTTCTTT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GGATATGTTGTGGAGCCGTATGTGGTTGCAGTAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AAAATACTGGGAGTACGTAAGAGCATTGCTGTGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GACAGAGGAGGAATCTTGGAAATTACGAGCTTTAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AACTACCGCTGTGAGCGCTCAAAACGACTTGCAAGCCATGAAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATGGCTTAATTTTAGCCTACAAGCTGCTTGAAACTTACAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTGAGACGCTTGGGGATGCCAGCCGTCACTTCAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAGGCATAGCTTACCTAGCTAAAATAACTCTTCT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATGTTCCACAGTGCAGAAGCGGATGAAACGATGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATCCCGATTATCACGGGAGTATCCTTACCAGATAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TATGACCACTACGGTAAGTATATTTGCGGTGCG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTCTGTTGTTCTCACAACGATAATTACTAACAAAAACT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTATGCCTCAAACCTTTCTCAAGTCATCAAACA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GTACTATCTAGACTGGCGCGAGAAAGTCTAAGACT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ACGTGCTTTCTAAACTTGCAGTGACCGCACCAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ACTTTACGTGCGTTAGCAACAGACGTAGACAAATC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTAAATCTCAGCAACAAACAGATTGAGGAAATT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTAATAGAGAAAGACGAAGTCTATTATGATTGGCAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AACTCAATAGGTTTGAACAAGCAGAAAATATTATA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AAATCTTGGTTTTTACAAGTTCAGTGGAATGATTCA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAATACCTTGCTCATACGTTATCCTAACCGGATAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCTAGACGACTTCTGAGAAGGCTCTCTGGCAGAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CGGGTGGTACGCGAGCAGCAGGTGGACCAATTGC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TGCAAAACAGTCACGTCACAAAGAGCGATCGCGGACTTA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC

>NZ_CP019636|11|3|4554512-4557231|CRT
ATTTTAATCTCTAATAGGGATTCGTATCAGTTGTAAC	TTTAGACCCATTTAGTGACAAATCAAACTGGAGCGAATAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTTGCTTGAATGAGCGCTCTTATCTTGTTGCAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTGTTGTCCTTCGTTTCATAATAGAAAATGGTG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GCAGGTTGGATTTCAGCATCTCAAGACTGGAGCCTTGAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CCTTGAAGAAGGCATTCGATGCTAAACTCATGATGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTGTCTGGACATTCTCTGGTGAGATGTTCAGTCGTC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTCTCTCTCCCAGTCAGCGCTGACAATAAAAGCT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GCTAGCCCATTTTAGCCAACACCCAAGAAACTAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAACTTGGGGTTTCTGTATATGCGCCAAAGTACATAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GAGAAGGTGTTGAATGGTTTGTAAGAAACAGTCGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTGCTAAGGAATTACTGAAGAGCATAGACCCACAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TACTCTTCGATGCGTTTTTCTGAGAGAATAGTGG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCTGAAGTACTTCAGAAATAAATAATCATAATAAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTTGTTCGTCTAACGTAAATGCTGAGTCTTCTTT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GGATATGTTGTGGAGCCGTATGTGGTTGCAGTAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AAAATACTGGGAGTACGTAAGAGCATTGCTGTGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GACAGAGGAGGAATCTTGGAAATTACGAGCTTTAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AACTACCGCTGTGAGCGCTCAAAACGACTTGCAAGCCATGAAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATGGCTTAATTTTAGCCTACAAGCTGCTTGAAACTTACAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTGAGACGCTTGGGGATGCCAGCCGTCACTTCAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAGGCATAGCTTACCTAGCTAAAATAACTCTTCT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATGTTCCACAGTGCAGAAGCGGATGAAACGATGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATCCCGATTATCACGGGAGTATCCTTACCAGATAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TATGACCACTACGGTAAGTATATTTGCGGTGCG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTCTGTTGTTCTCACAACGATAATTACTAACAAAAACT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTATGCCTCAAACCTTTCTCAAGTCATCAAACA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GTACTATCTAGACTGGCGCGAGAAAGTCTAAGACT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ACGTGCTTTCTAAACTTGCAGTGACCGCACCAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ACTTTACGTGCGTTAGCAACAGACGTAGACAAATC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTAAATCTCAGCAACAAACAGATTGAGGAAATT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTAATAGAGAAAGACGAAGTCTATTATGATTGGCAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AACTCAATAGGTTTGAACAAGCAGAAAATATTATA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AAATCTTGGTTTTTACAAGTTCAGTGGAATGATTCA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAATACCTTGCTCATACGTTATCCTAACCGGATAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCTAGACGACTTCTGAGAAGGCTCTCTGGCAGAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CGGGTGGTACGCGAGCAGCAGGTGGACCAATTGC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TGCAAAACAGTCACGTCACAAAGAGCGATCGCGGACTTA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC

>NZ_CP019636|11|3|4554589-4557231|PILER-CR
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTTGCTTGAATGAGCGCTCTTATCTTGTTGCAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTGTTGTCCTTCGTTTCATAATAGAAAATGGTG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GCAGGTTGGATTTCAGCATCTCAAGACTGGAGCCTTGAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CCTTGAAGAAGGCATTCGATGCTAAACTCATGATGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTGTCTGGACATTCTCTGGTGAGATGTTCAGTCGTC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTCTCTCTCCCAGTCAGCGCTGACAATAAAAGCT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GCTAGCCCATTTTAGCCAACACCCAAGAAACTAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAACTTGGGGTTTCTGTATATGCGCCAAAGTACATAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GAGAAGGTGTTGAATGGTTTGTAAGAAACAGTCGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTGCTAAGGAATTACTGAAGAGCATAGACCCACAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TACTCTTCGATGCGTTTTTCTGAGAGAATAGTGG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCTGAAGTACTTCAGAAATAAATAATCATAATAAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTTGTTCGTCTAACGTAAATGCTGAGTCTTCTTT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GGATATGTTGTGGAGCCGTATGTGGTTGCAGTAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AAAATACTGGGAGTACGTAAGAGCATTGCTGTGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GACAGAGGAGGAATCTTGGAAATTACGAGCTTTAC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AACTACCGCTGTGAGCGCTCAAAACGACTTGCAAGCCATGAAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATGGCTTAATTTTAGCCTACAAGCTGCTTGAAACTTACAA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTGAGACGCTTGGGGATGCCAGCCGTCACTTCAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAGGCATAGCTTACCTAGCTAAAATAACTCTTCT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATGTTCCACAGTGCAGAAGCGGATGAAACGATGT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ATCCCGATTATCACGGGAGTATCCTTACCAGATAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TATGACCACTACGGTAAGTATATTTGCGGTGCG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CTCTGTTGTTCTCACAACGATAATTACTAACAAAAACT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTTATGCCTCAAACCTTTCTCAAGTCATCAAACA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	GTACTATCTAGACTGGCGCGAGAAAGTCTAAGACT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ACGTGCTTTCTAAACTTGCAGTGACCGCACCAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	ACTTTACGTGCGTTAGCAACAGACGTAGACAAATC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTAAATCTCAGCAACAAACAGATTGAGGAAATT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TTAATAGAGAAAGACGAAGTCTATTATGATTGGCAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AACTCAATAGGTTTGAACAAGCAGAAAATATTATA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	AAATCTTGGTTTTTACAAGTTCAGTGGAATGATTCA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCAATACCTTGCTCATACGTTATCCTAACCGGATAT
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TCTAGACGACTTCTGAGAAGGCTCTCTGGCAGAG
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	CGGGTGGTACGCGAGCAGCAGGTGGACCAATTGC
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC	TGCAAAACAGTCACGTCACAAAGAGCGATCGCGGACTTA
GTTTCAATCCCTAATAGGGATTCGTATGAATTGTAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087546254.1\|4551518_4552880_+\|M28-family-peptidase	unknown	unknown	gnl\|CDD\|349874
NZ_CP019636.1\|WP_087546255.1\|4553832_4554462_+\|Uma2-family-endonuclease	unknown	unknown	gnl\|CDD\|368559
NZ_CP019636.1\|WP_087541653.1\|4569122_4571471_+\|DUF4101-domain-containing-protein	unknown	unknown	gnl\|CDD\|372576
NZ_CP019636.1\|WP_087541645.1\|4550958_4551450_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541651.1\|4566363_4567200_-\|aldose-epimerase	unknown	unknown	gnl\|CDD\|185702
NZ_CP019636.1\|WP_087541646.1\|4552955_4553747_+\|trypsin-like-serine-protease	unknown	unknown	gnl\|CDD\|273938
NZ_CP019636.1\|WP_087541652.1\|4567353_4568391_-\|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha	unknown	unknown	gnl\|CDD\|177069
NZ_CP019636.1\|WP_087541655.1\|4573170_4574412_+\|DUF4912-domain-containing-protein	unknown	unknown	gnl\|CDD\|225867
NZ_CP019636.1\|WP_087541650.1\|4564869_4565949_-\|fructose-bisphosphate-aldolase-class-II	unknown	unknown	gnl\|CDD\|181691
NZ_CP019636.1\|WP_087541654.1\|4571697_4572687_+\|transporter	unknown	unknown	gnl\|CDD\|223751
NZ_CP019636.1\|WP_087541643.1\|4550126_4550507_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541656.1\|4574733_4575675_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378342
NZ_CP019636.1\|WP_087541644.1\|4550538_4550946_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541642.1\|4548601_4549882_+\|two-component-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|274368
NZ_CP019636.1\|WP_087541649.1\|4561241_4564442_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|236842
NZ_CP019636.1\|WP_087541641.1\|4547851_4548529_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP019636.1\|WP_087541640.1\|4547379_4547778_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541639.1\|4546507_4547101_-\|MarC-family-protein	unknown	unknown	gnl\|CDD\|225006
NZ_CP019636.1\|WP_087541648.1\|4559270_4561214_+\|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl\|CDD\|213023
NZ_CP019636.1\|WP_087541647.1\|4557956_4558775_+\|carbon-nitrogen-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|143596

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087546254.1\|4551518_4552880_+\|M28-family-peptidase	gnl\|CDD\|349874	cd03877, M28_like, M28 Zn-peptidase, many containing a protease-associated (PA) domain insert. Peptidase family M28 (also called aminopeptidase Y family), uncharacterized subfamily. The M28 family contains aminopeptidases as well as carboxypeptidases. They have co-catalytic zinc ions; each zinc ion is tetrahedrally co-ordinated, with three amino acid ligands plus activated water; one aspartate residue binds both metal ions. This subfamily is composed of uncharacterized proteins, many of which contain a protease-associated (PA) domain insert which may participate in substrate binding and/or promote conformational changes, influencing the stability and accessibility of the site to substrate. Some proteins in this subfamily are also associated with the PDZ domain, a widespread protein module that has been recruited to serve multiple functions during the course of evolution.	1.45024e-42
NZ_CP019636.1\|WP_087546255.1\|4553832_4554462_+\|Uma2-family-endonuclease	gnl\|CDD\|368559	pfam05685, Uma2, Putative restriction endonuclease. This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. A small number of member proteins also contain pfam02861 domains that are involved in protein interactions. Solutions of several structures for members of this family show that it is likely to be acting as an endonuclease.	1.10238e-19
NZ_CP019636.1\|WP_087541653.1\|4569122_4571471_+\|DUF4101-domain-containing-protein	gnl\|CDD\|372576	pfam13355, DUF4101, Protein of unknown function (DUF4101). This is a family of uncharacterized proteins, and is sometimes found in combination with pfam00226.	1.3532e-35
NZ_CP019636.1\|WP_087541646.1\|4552955_4553747_+\|trypsin-like-serine-protease	gnl\|CDD\|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	2.01721e-79
NZ_CP019636.1\|WP_087541652.1\|4567353_4568391_-\|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha	gnl\|CDD\|177069	CHL00149, odpA, pyruvate dehydrogenase E1 component alpha subunit; Reviewed.	0
NZ_CP019636.1\|WP_087541647.1\|4557956_4558775_+\|carbon-nitrogen-hydrolase-family-protein	gnl\|CDD\|143596	cd07572, nit, Nit1, Nit 2, and related proteins, and the Nit1-like domain of NitFhit (class 10 nitrilases). This subgroup includes mammalian Nit1 and Nit2, the Nit1-like domain of the invertebrate NitFhit, and various uncharacterized bacterial and archaeal Nit-like proteins. Nit1 and Nit2 are candidate tumor suppressor proteins. In NitFhit, the Nit1-like domain is encoded as a fusion protein with the non-homologous tumor suppressor, fragile histidine triad (Fhit). Mammalian Nit1 and Fhit may affect distinct signal pathways, and both may participate in DNA damage-induced apoptosis. Nit1 is a negative regulator in T cells. Overexpression of Nit2 in HeLa cells leads to a suppression of cell growth through cell cycle arrest in G2. These Nit proteins and the Nit1-like domain of NitFhit belong to a larger nitrilase superfamily comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13), this subgroup corresponds to class 10.	1.3742e-138
NZ_CP019636.1\|WP_087541655.1\|4573170_4574412_+\|DUF4912-domain-containing-protein	gnl\|CDD\|225867	COG3330, COG3330, Uncharacterized protein conserved in bacteria [Function unknown].	1.49804e-96
NZ_CP019636.1\|WP_087541649.1\|4561241_4564442_-\|PAS-domain-S-box-protein	gnl\|CDD\|236842	PRK11091, PRK11091, aerobic respiration control sensor protein ArcB; Provisional.	6.55724e-59
NZ_CP019636.1\|WP_087541650.1\|4564869_4565949_-\|fructose-bisphosphate-aldolase-class-II	gnl\|CDD\|181691	PRK09196, PRK09196, fructose-bisphosphate aldolase class II.	0
NZ_CP019636.1\|WP_087541656.1\|4574733_4575675_+\|hypothetical-protein	gnl\|CDD\|378342	pfam09992, NAGPA, Phosphodiester glycosidase. This is a family conserved from bacteria to humans. The structure of a member from Bacteroides has been crystallized and modelled onto the luminal region of the human member of the family, the transmembrane glycoprotein N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase. There is some conservation of potentially functional residues, implying that in the bacterial members this family acts in some way as a phosphodiester glycosidase. The human protein is also present, so the eukaryotic members are likely to be catalyzing the second step in the formation of the mannose 6-phosphate targeting signal on lysosomal enzyme oligosaccharides.	8.29685e-05
NZ_CP019636.1\|WP_087541642.1\|4548601_4549882_+\|two-component-sensor-histidine-kinase	gnl\|CDD\|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	2.92876e-58
NZ_CP019636.1\|WP_087541641.1\|4547851_4548529_+\|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].	4.22625e-76
NZ_CP019636.1\|WP_087541654.1\|4571697_4572687_+\|transporter	gnl\|CDD\|223751	COG0679, COG0679, Predicted permeases [General function prediction only].	2.13591e-31
NZ_CP019636.1\|WP_087541639.1\|4546507_4547101_-\|MarC-family-protein	gnl\|CDD\|225006	COG2095, MarC, Multiple antibiotic transporter [Intracellular trafficking and secretion].	1.5722e-46
NZ_CP019636.1\|WP_087541648.1\|4559270_4561214_+\|polysaccharide-deacetylase-family-protein	gnl\|CDD\|213023	cd10918, CE4_NodB_like_5s_6s, Putative catalytic NodB homology domain of PgaB, IcaB, and similar proteins which consist of a deformed (beta/alpha)8 barrel fold with 5- or 6-strands. This family belongs to the large and functionally diverse carbohydrate esterase 4 (CE4) superfamily, whose members show strong sequence similarity with some variability due to their distinct carbohydrate substrates. It includes bacterial poly-beta-1,6-N-acetyl-D-glucosamine N-deacetylase PgaB, hemin storage system HmsF protein in gram-negative species, intercellular adhesion proteins IcaB, and many uncharacterized prokaryotic polysaccharide deacetylases. It also includes a putative polysaccharide deacetylase YxkH encoded by the Bacillus subtilis yxkH gene, which is one of six polysaccharide deacetylase gene homologs present in the Bacillus subtilis genome. Sequence comparison shows all family members contain a conserved domain similar to the catalytic NodB homology domain of rhizobial NodB-like proteins, which consists of a deformed (beta/alpha)8 barrel fold with 6 or 7 strands. However, in this family, most proteins have 5 strands and some have 6 strands. Moreover, long insertions are found in many family members, whose function remains unknown.	5.54273e-51
NZ_CP019636.1\|WP_087541651.1\|4566363_4567200_-\|aldose-epimerase	gnl\|CDD\|185702	cd09025, Aldose_epim_Slr1438, Aldose 1-epimerase, similar to Synechocystis Slr1438. Proteins similar to Synechocystis Slr1438 are uncharacterized members of 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.	9.206e-145

>NZ_CP019636.1|WP_087546255.1|4553832_4554462_+|Uma2-family-endonuclease
MDTIITPEKIELPPGTVVRMLGNWHDYERLQQQLGDRSIPRVKYRPGEILLMSPLPEHGRKAGLTARIVTTLLDYLNRQYEEFSPITMSLPEVRGIEPDYCFYIENWAAVAGKDRIDWQNDPPPNLAIEVDVTSYTDINDYLPYRVPEVWLLRNNQLLVYRLQGSSYVLAESSYFPNVSEIVRQCLQIASEQTTSEAIRWLRNFLYKQQ
>NZ_CP019636.1|WP_087541646.1|4552955_4553747_+|trypsin-like-serine-protease
MSSFISLKKSLSNLSLVSLGAATALLGAHFMPTNPVLSQQPIAQLPSAPIGNTETNFVASAVERTGSAVVRIDSTRTVRSPYTYGRRVARGTGSGFIIRSNGLILTNAHVVGGADTVTVTLKDGRSFTGRVVGQDRSTDVAVVQIQANNLPVVSIGNSDQLKPGEWAIAIGNPLGLDNTVTVGIISGTDRSSRAFGSRGRGVGFIQTDAAINPGNSGGPLLNQRGQVIGVNTAIIQGAQGLGFAIPINLAQQIANQLIAQAAA
>NZ_CP019636.1|WP_087546254.1|4551518_4552880_+|M28-family-peptidase
MFLLQRNLAKSWLQTVLVAVVVGLPTACVAQSNSAREVSHSQSVVETHTKLHSKTSPRPLGTPLLRKERGGGEVTPMNATRYQQSNSTFADVQTLVNLGPRVAGTPVMEKASTYLLDEYRKAGYVTEVQTFNYSKFEDLGSNLTVDGTTVQGKALSGTVPGKLNAPLVAVPNVGRQADFAAVNVKGAIAIVRRGEIRFSEKAKNASAAGAVGLVIVNNEPGNVYGTLGEEVKIPVLALSGKQGNPLIQRVQTASVNVNLNVNAQRRDVTGHNIIAHLEGVTQPKIILGGHYDSVPGSPGANDNASGTAVVLALARNLSNTPTARQAWFVAFDGEEDGLHGSRAFVNTAGSQFLSELKAMVNFDMVGVNDQLGIGGTSSLTTFARNLEPTVKTFGSFGGSDHAPFADKGVPVLFFYRGQEPNYHTPGDKKVDLKLLNETTQVALDIVKQIVSVN
>NZ_CP019636.1|WP_087541645.1|4550958_4551450_+|hypothetical-protein
MNIADTSWWLWLENSPLSSAIRQWLWLYPMISTTHILGLAIVFGSVAMFDLRLLGFSRHLLVTDMARHLLPWSFLSFVVVVLSGFLMFAVDATDIAANPAFRLKLLLLCAAGMNAAFFHRVAFKSVKFWNRGVKTPIVVRAIAVISLVLWTGVILCGRLIAYT
>NZ_CP019636.1|WP_087541644.1|4550538_4550946_+|hypothetical-protein
MDNQQPINKAMLKKSFVQAALTAATIATFLASGTENASAHHGWSEYNNEQTLNLTGEIQNVNYDNPHTTIEVKTDDNKVWQAVLAPPARLQRRGLPEGSLQVGQRVKLVGYPHRTDTNEMRAERIIIGKQTVELR
>NZ_CP019636.1|WP_087541643.1|4550126_4550507_+|hypothetical-protein
MISRSQFFWITVITVVVSLAFAGEVAAHHGYDTTYDIGHPRTITGVIKAVRYASPHIRMQLQTTGDSKQVWRIDLPSPTQAERRGVTRDFLKVGATATVLGWPAYDGSNEMGASQITIGGKTVQVN
>NZ_CP019636.1|WP_087541642.1|4548601_4549882_+|two-component-sensor-histidine-kinase
MFIRSRRNLAYLFTISMGSILIVFAGLAYYLVVQQQLQAFDDKLYSESKAIARNLLYRLYNKQWQVQRRDPPIYSDTVPEINNGFAYLRWYNSNGELVDSIGVSGSRKLTVVPGFQTIKINKNRDRETTTKEWLRELTLPVIQDNFLIGYIQVAAPLTPLRKNLNKARFFLTLSLPVALGTIGITGWFLGGLAMQPTRRAYEQLQRFTADASHELRAPVAAILSNAQVALMPPRDELEQHFRLENIAGIAKSMSNLINNLLFLARQDGPLDTITLKTIDLVGLLRSIAQEYQQQAVTQNLNFTFHIPESPVNLKADLDLLKQAIINLLSNAFKYTPDEGTVTLKLLTQSHKAIIQVEDDGIGIPEEDLPHIFERFYRVDAARSRQTGGFGLGLAIAQQIVQAHRGQITAKSLLGQGSTFKIELPLK
>NZ_CP019636.1|WP_087541641.1|4547851_4548529_+|response-regulator-transcription-factor
MLILLVEDDLAQLEPLRAALTKAGHNVDAIEDGETAQWLLSQKNYDLLILDWMLPKVSGVDLCLEYRRAGKTAPVMMLTAKDTTSDKVYGLDAGADDYLVKPVDIIELLARVRALRRRSPLWQGDKLTLADLHLDLNNLTIERNQLTTQLSGREFQLMEYLMRHPRQILSHNQIEQTLWGWGTEPESNAVTTLVRRLRQRLQTVGAKDWLENVYGMGYRLNVPEK
>NZ_CP019636.1|WP_087541640.1|4547379_4547778_-|hypothetical-protein
MLQSRWLKILRSLGLEFWLPLPLLGLAFWVGGGFVMNGILSSSHQPTSPLKAETLSAKQPRTIVVSITAKIKKHQGVSRVRVKTASKLLKELEFEFPVTEFSQVEAAISQELRLPISDVRKLMHYTTENGME
>NZ_CP019636.1|WP_087541639.1|4546507_4547101_-|MarC-family-protein
MDISILVKTFIAVFVLADAVGNIPILLVLTKGMEPENRSRVIDKAIVVAIAVLLLFAFAGQLILSYLDISLGSLRVAGGLLLLLIALQMLQGDLDTPVIDQERDVAITPLALPLLAGPGTLTSVMLLMSESPSPHISVIVGIVAAMFSSWLILRLASGIDKWIGVEGEVIITQLLGFLLAALAVEIGSAGIKELFLS
>NZ_CP019636.1|WP_087541647.1|4557956_4558775_+|carbon-nitrogen-hydrolase-family-protein
MKSYLAAAIQMTSVPNIQKNLAQAEEFIDLAVRQGAELIGLPENFAFMGEENEKMAQAEAIAQETEKFLRTMAQRFQVTILGGGFPVPVDNTSNRVYNTALLIDPSGQELARYQKVHLFDVNVPDGNTYRESATVMAGKQLPPVYFSQELGNIGLSVCYDVRFPELYRHIAYKGGDVIFVPAAFTAFTGKDHWQVLLQARAIENTCYVIAPAQTGINYARRQTHGHAMIIDPWGVILADAGEQPGVAIAEINPLRLEQVRRQMPSLQHRVFV
>NZ_CP019636.1|WP_087541648.1|4559270_4561214_+|polysaccharide-deacetylase-family-protein
MKLIPNHCILKYIFLNFHSRIIFSALICGLFTASGLLPQMSVAQSSASQQVEPDSTTTTSESCSNNAMSLNNQVSRVADNLVLASTWVSKPNWGLENIVGAIGPYVFAFLNRSAWPSINERAKQARVPIVMYHDILPKKQVFFDVTPEELEQHFQLLKENGITPISLDQLMTHLQTGMPLPEKPVLLTFDDGYGGHYEYVYPLLKKYGYPAVFSIYTKGVGNNAGRTHVSWEQLKEMADDPLVTIASHSVSHPPDLTVLPPEQIQKEVVESKAMLEATLGIPIRYFTYPAGKYNEQVASLVQAAGYDLALTMNDVDERFAGQSESLLAVSRFGQSRIKDVITQAWGGPQLPSWKIGFDFASPVQRTDLTIDKIPLILVSGGKPITIHADSRYTVKEILAKSNTNAVAAVDGGFFSLKSLNSNVMIGPVLSQVTKQFIPGNNGDNQKLGGRPLVLVSPHEVRFIPFDPLKHNTLEGIQAEMPEVTDAFVAAAWLVKDGQPREASTFNGLFGFDAPRYRAFWGINQNKQATIGVSLESVDSISLGVALVKAGLQDVVMVDSGQSTSLVYHGESLVRYEPRPVPHAVALLAPPSMANSSCVLVENKTKQQTDTAVSVLSKEKTSVRGTVHALRSHSYKRFVQNKTKHRRT
>NZ_CP019636.1|WP_087541649.1|4561241_4564442_-|PAS-domain-S-box-protein
MIQRTSWRLKHTETIRNRLLTYGVAIVSIVIALVLMVVLDPWLEMTKSPFLLFFGAIMLSAWYGGHKPGVFATLLSALTANYLFMGNSRYEFALDAINISRVLIFILEGILISTLSGALLKAQKRTQQSLQLLQVSEAKFRRLVDSDIIGVVSCDIYGAITEANNAFLKMVGYTQEDVLAERVRWDDMTPPDLRHLDVPAYEELMTKGKNSPYEKAFIAKDGRRVPIIVGAAIIEDESRENVISFVLDLTRLKQTEKALRESEEKYRRIVETANEGIWLNDAQSQTTYVNSRLAQMLGYSMEEMLGRSAFDYVDKTDLAEAKRNFKHKKQGLTEEHDFRLRRKDGSSVWILSRSSRIFSENGELLGILSMVTDVTERKRSEQRKLLQYAVSRVLAEAKTVGDAMPAILQSLCESLGWQLGIFWGLEHQSNLLYYTNHWHIPSLDVKEFTEVKQRITFALGEGLPGCVWASGQPTWIVDLIEDENFPRASAAVKVGLHGVFAFPIRLEQEILGVIECFSDKVQEPDEDLLEMMASIGSEIGQFIERKRAEEELAKSQQLFWSFMNNIPGTAFIKDEEGHYLFVNPVTEHWTNCKQADILGKTDFDILSSEIAQQIRENDKVVLAAGKPIEIQETLPQSDGERYWMSFKFPIEDVSGKKMLAGMSFDITERKQLENRLQQQATELAQANSIKDEFLAVLSHELRSPLNPILGWAKLLRTRKFDEATVARALETIERNAQVQIQIIADLLDISRIIRGQLNLNISSVNLVSIVEAAIETVRLAAEAKAIEMNLDIHANHAVVLGDSSRLQQIVWNFLSNAVKFTPNGGRVDVRLESIGTNAHITVSDTGKGINPNFLPYVFDYFRQENSTTNRQFGGLGLGLAIVRRLVEFHGGSVKADSPGVGQGATFTVTLPLKTAVQQMNNHRDMKSDDLPNLKGLRVLVVDDDADNLDLITFILEEYGVEVRALASAKEVLSVLAEWHPDLLLSDIGMPEVDGYTLIRQIRALPEELGGQVRAIALTAYAGEMNQQQALSAGFEKHVTKPVDPTELALAIANAVGQMNRVNYSSG
>NZ_CP019636.1|WP_087541650.1|4564869_4565949_-|fructose-bisphosphate-aldolase-class-II
MALVPLRLLLDHAAENGYGIPAFNVNNLEQIQAIVQAAHETDSPVILQASRGARKYAGENFLRHLILAAVETYPHIPITMHQDHGNEPATCYSAIKNGFTSVMMDGSLEADAKTPASYEYNVNTTREVVKVAHSLGVSVEGELGCLGSLETGQGEAEDGHGFEGTLSHDQLLTDPDQAVDFVEQTQVDALAVAIGTSHGAYKFTRKPTGEILAISRIEEIHRRLPNTHLVMHGSSSVPEDLIAIINEYGGAIPETYGVPVEEIQKGIKSGVRKVNIDTDNRLAITAAVREALAKAPKEFDPRHFLKPSIKYMQKVCVDRYQQFGTAGNASKIKQISLEEFAAKYAKGELNAVTKKTAIV
>NZ_CP019636.1|WP_087541651.1|4566363_4567200_-|aldose-epimerase
MNKRSIQTNQSRLEVVPERGGIITSWRVQGQEILFLDEERFANPQLSVRGGIPILFPICGNLPGNTYTYNGKEYTLKQHGFARDLPWKPVEDQVTPEKASLTLVLTSNEQTRAVYPFDFELTFTYQIQGNTLEIKQKYKNLSTEQMPFSTGLHPYFFTADKTQLQFEIPSREYQDQITKECHQFHGNFDYTRDEIDVAFKQLSSQSAIVTDNSRKLKLTLEYDETYPTLVFWTVKGKDYYCLEPWSAPRNSLNTGEHLTVLAPEAEREAIVRLTANFF
>NZ_CP019636.1|WP_087541652.1|4567353_4568391_-|pyruvate-dehydrogenase-(acetyl-transferring)-E1-component-subunit-alpha
MVTERTLPKFDAATVQITKEEGLQLYEDMMLGRLFEDKCAEMYYRGKMFGFVHLYNGQEAVSSGVIRGAMRPGEDFVCSTYRDHVHALSAGVPAKEVVAELFGKSTGCSKGRGGSMHMFSAKHRLLGGYAFVAEGIPVASGAAFQTKYRREVLGDESADQVTACFFGDGAANNGQFFETLNMAALWKLPILFVVENNKWAIGMAHERATSQPEIYQKASVFNMAGVEVDGMDVLAVRAVAQEAVARARAGEGPTLIEALTYRFRGHSLADPDELRTKTEKEYWFARDPIKKFAAYLVEHNLSSEEELKNIDRQVQQVIDEAVKFAESSPEPDPSELYRFIFAEDE
>NZ_CP019636.1|WP_087541653.1|4569122_4571471_+|DUF4101-domain-containing-protein
MRIPLDYYRILGIPMAASEEQLRQAYGDRIVQLPRREYSQAAITSRKNLIEEAYAVLSNPKERITYDQLYLAHAYGSDSTQGGVVAVESREQSKFDNTEYQSLNIEISQDELVGALLILQELGEYELVLKLGRPYLINRNGTPLSIQGNGEDTEESPSTAAERPDVVLTVSLACLELGREQWQQSHYENAAISLETGEELLAREGLFPTVRAEIQSDLYRLRPYRILELLALPEEQTSERQQGLQLLQDILDERSGIDGTGDDKSGLNIDDFLRFIQQLRNYLTVVEQHKLFEMESRRPSAVATYLAVYASIARGFTQRQPALIRQAKQMLIRLGRRQDVHLEQSLCALLLGQTEEASRALELSQEYEALAFIRENSQDSPDLLPGLCLYGERWLENELFPNFRDLVKQPASLKDYFADKQVQAYLEALPTEAEPINQGTGIHRQSSQTQETTRRSRRNNSAVGQEQYQNKQTPNPGTQATPTPQKPESSNYSSPSYTTPPPSSGSSWSLNAQTPVAPPANIDPTATGTYRNLNGRFKASAVPPQPQTQRRHKRSSSTSSQRGLDKRHGQVHRRRVFARTSPAQIRFVFIVLASLVSLVVLWILTAATIGLFKPLFFPGPSLKGEQLSVQLNEPPVPIPDQNSKPQLPAGSLTEETAGEMVQAWLDTKAAALGYNHEIDSLDHILVGSTLTKWRGLAKQERTDNRYRKYQHSVKVESLETNQANQNHAAVEASVTEVTEYYENGQVKKSDNEKLRVRYELVRVEGTWRIQDMSVLNKLSMIS
>NZ_CP019636.1|WP_087541654.1|4571697_4572687_+|transporter
MTETLFHAYAPLILWTSLGLLIFKFLPQWFPRLLGRCLYWFGVPLELLALARQRGFNEFAGEVSLPILAPIITLGVLVLGLVMTSLILKGWKLLLSDKLKPYSAKLFPPYLLDSSSSGSFVISAVLGNTGFVGLAIAPSLVSSDGVNWAVLYSITHNVIGTYGFGVVIASYFSHSQQQNRWWMQLRDVLSVPSLWAFLFGYLTRSVQLPEIIESGLQGSVNIVIACAFLLTGIRLAQLQGWKSLKLAFVPAFLRVFLTPLLVGLATTLFFGLSGSPRLAMVLMSGVPTAFAGLILAEEYNLDRDLITSSIIISTLLLLLVLPLWILVFG
>NZ_CP019636.1|WP_087541655.1|4573170_4574412_+|DUF4912-domain-containing-protein
MAKERPPLEEMTLRQLRKVASEYGVSRYSRMRKSQLLASIQEVQRSKVSLSQSRSLEAQETVEAAKFELGQVDRTGGTLADVDEGLGDLPQGYGESRIVLLPRDPQWAYTYWDVPNEHKEELRRQGGQQLALRIYDVTDINLEYQSPHSIQEYPSDELAREWYLPIPVSDRDYVIDIGYRCADGRWLTLARSAPVHVPPVYPSDWIEDVFITVNFEEDLRGKTVYELVPPTKKVPTATANGANPIYDQIFGLAESAEAQRVAGSLFGSMQHVPGSVTPEQAISSYIFPSGVGMWAVPTVSGLTASGVGMSGAGFSGDVPMRPRKFWLIADAELIVYGATEPDATVTIGGRPIKLNPDGTFRFQMSFQDGLIDYPIMAVAADGEQTRSIHMKFTRETPSRNTNTKEEAVLEWLS
>NZ_CP019636.1|WP_087541656.1|4574733_4575675_+|hypothetical-protein
MLKSKFIYFFKVIIIFTLCLACQKTSQTSATTQVSKQCIGNNTKSSIEFLKTNNQGKKDARGINHVIIFNPKSKELDFKVNLGLSHQLYAKNNQGKLRQEYIPKSFHELITDENAKLNGQTPIAAINADYIDIDHKPQGLNISRGVEYSGAFKNKRSSFGISAGKPEQRQATIQVGRRKEKILNYNLVGGNGRFYRNGKFKDICQDLGELACKQATNRSMVAITNKGYVILLVNDIKANSNLELSQLNQELMPNMFDDVLEGIARNNCLGKIQEGMLFDGGMSPGLYYNKKIYVENPGQIGSVFLIYQRPLNN

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Crispr_ID: NZ_CP019636_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_12

4772008-4772151

Orphan

Consensus_repeat	Method
CAACTCGTCAACGAGTATCGAAGACTCAAGCGCGAGTAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_12

>merge|NZ_CP019636|12|4772008-4772151|CRISPRCasFinder
AACCTCGTGAACAAGTATCAACAACTCGTCAACGAGTATCGAAGACTCAAGCGCGAGTATAAAAGTCTTGTGAATGAGTATTAGAAACTCACCAACGAATATCAGCAACTCGTCAACGAGTATCAAAGACTCAAGCGCGAGTAT

>NZ_CP019636|12|12|4772008-4772151|CRISPRCasFinder
AACCTCGTGAACAAGTATCAACAACTCGTCAACGAGTAT	CGAAGACTCAAGCGCGAGTATAAAAGTCTTGTGAATGAGTATTAGAAACTCACCAACGAATATCAG
CAACTCGTCAACGAGTATCAAAGACTCAAGCGCGAGTAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087541798.1\|4765059_4766184_-\|ferrochelatase	unknown	unknown	gnl\|CDD\|223353
NZ_CP019636.1\|WP_087541799.1\|4766767_4767340_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546264.1\|4777569_4779966_-\|histidine-kinase	unknown	unknown	gnl\|CDD\|185504
NZ_CP019636.1\|WP_087541811.1\|4787483_4787951_-\|DUF4870-domain-containing-protein	unknown	unknown	gnl\|CDD\|225833
NZ_CP019636.1\|WP_087541809.1\|4785131_4785602_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|182099
NZ_CP019636.1\|WP_087541804.1\|4775581_4776979_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546261.1\|4761331_4762030_+\|M23-family-metallopeptidase	unknown	unknown	gnl\|CDD\|366703
NZ_CP019636.1\|WP_087541796.1\|4760295_4760685_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541797.1\|4764450_4764996_+\|NAD(P)H-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223508
NZ_CP019636.1\|WP_087541801.1\|4769097_4770975_+\|biosynthetic-type-acetolactate-synthase-large-subunit	unknown	unknown	gnl\|CDD\|236014
NZ_CP019636.1\|WP_087541800.1\|4767685_4768954_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340863
NZ_CP019636.1\|WP_157679554.1\|4771055_4771694_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541807.1\|4783062_4783749_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237019
NZ_CP019636.1\|WP_087541808.1\|4784095_4784704_-\|thermonuclease-family-protein	unknown	unknown	gnl\|CDD\|224442
NZ_CP019636.1\|WP_087541806.1\|4780048_4781635_-\|mechanosensitive-ion-channel-family-protein	unknown	unknown	gnl\|CDD\|366370
NZ_CP019636.1\|WP_087546263.1\|4772191_4772839_-\|GUN4-domain-containing-protein	unknown	unknown	gnl\|CDD\|319862
NZ_CP019636.1\|WP_087546262.1\|4762102_4763980_-\|ATP-dependent-zinc-metalloprotease-FtsH	unknown	unknown	gnl\|CDD\|214386
NZ_CP019636.1\|WP_087537548.1\|4781922_4782801_-\|IS982-family-transposase	unknown	unknown	gnl\|CDD\|372648
NZ_CP019636.1\|WP_087541795.1\|4758755_4759985_+\|calcium-binding-protein	unknown	unknown	gnl\|CDD\|380205
NZ_CP019636.1\|WP_087541810.1\|4786249_4787359_-\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087541798.1\|4765059_4766184_-\|ferrochelatase	gnl\|CDD\|223353	COG0276, HemH, Protoheme ferro-lyase (ferrochelatase) [Coenzyme metabolism].	2.11253e-86
NZ_CP019636.1\|WP_087541807.1\|4783062_4783749_-\|hypothetical-protein	gnl\|CDD\|237019	PRK11907, PRK11907, bifunctional 2',3'-cyclic-nucleotide 2'-phosphodiesterase/3'-nucleotidase.	0.00497918
NZ_CP019636.1\|WP_087546264.1\|4777569_4779966_-\|histidine-kinase	gnl\|CDD\|185504	PTZ00184, PTZ00184, calmodulin; Provisional.	2.95474e-44
NZ_CP019636.1\|WP_087541809.1\|4785131_4785602_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|182099	PRK09831, PRK09831, GNAT family N-acetyltransferase.	1.20194e-24
NZ_CP019636.1\|WP_087541811.1\|4787483_4787951_-\|DUF4870-domain-containing-protein	gnl\|CDD\|225833	COG3296, COG3296, Uncharacterized protein conserved in bacteria [Function unknown].	7.07044e-33
NZ_CP019636.1\|WP_087546261.1\|4761331_4762030_+\|M23-family-metallopeptidase	gnl\|CDD\|366703	pfam01551, Peptidase_M23, Peptidase family M23. Members of this family are zinc metallopeptidases with a range of specificities. The peptidase family M23 is included in this family, these are Gly-Gly endopeptidases. Peptidase family M23 are also endopeptidases. This family also includes some bacterial lipoproteins for which no proteolytic activity has been demonstrated. This family also includes leukocyte cell-derived chemotaxin 2 (LECT2) proteins. LECT2 is a liver-specific protein which is thought to be linked to hepatocyte growth although the exact function of this protein is unknown.	9.59841e-22
NZ_CP019636.1\|WP_087541806.1\|4780048_4781635_-\|mechanosensitive-ion-channel-family-protein	gnl\|CDD\|366370	pfam00924, MS_channel, Mechanosensitive ion channel. Two members of this protein family of M. jannaschii have been functionally characterized. Both proteins form mechanosensitive (MS) ion channels upon reconstitution into liposomes and functional examination by the patch-clamp technique. Therefore this family are likely to also be MS channel proteins.	1.68343e-33
NZ_CP019636.1\|WP_087537548.1\|4781922_4782801_-\|IS982-family-transposase	gnl\|CDD\|372648	pfam13612, DDE_Tnp_1_3, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contains three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.47625e-91
NZ_CP019636.1\|WP_087541801.1\|4769097_4770975_+\|biosynthetic-type-acetolactate-synthase-large-subunit	gnl\|CDD\|236014	PRK07418, PRK07418, acetolactate synthase large subunit.	0
NZ_CP019636.1\|WP_087541800.1\|4767685_4768954_+\|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.	7.46849e-62
NZ_CP019636.1\|WP_087541810.1\|4786249_4787359_-\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.34816e-71
NZ_CP019636.1\|WP_087541795.1\|4758755_4759985_+\|calcium-binding-protein	gnl\|CDD\|380205	NF033203, entero_EhxA, enterohemolysin EhxA. Members of this family are the RTX toxin called enterohemolysin or EhxA, because it is found in enterohemorrhagic Escherichia coli (EHEC) strains such as O157:H7.	7.23329e-17
NZ_CP019636.1\|WP_087546263.1\|4772191_4772839_-\|GUN4-domain-containing-protein	gnl\|CDD\|319862	cd16383, GUN4, porphyrin-binding protein domain GUN4. GUN4 is a porphyrin-binding protein involved in chlorophyll biosynthesis regulation and intracellular signaling, found in aerobic photosynthetic organisms. It has been implicated in retrograde signalling between the chloroplast and nucleus. GUN4 can bind protoporphyrin IX (PIX) and magnesium protoporphyrin IX (MgPIX), substrate and product of the Mg-chelatase, as well as heme and cobalt protoporphyrin IX (CoPIX). It may play a role in protecting plants from reactive oxygen species (ROS)-mediated damage.	9.54487e-72
NZ_CP019636.1\|WP_087546262.1\|4762102_4763980_-\|ATP-dependent-zinc-metalloprotease-FtsH	gnl\|CDD\|214386	CHL00176, ftsH, cell division protein; Validated.	0
NZ_CP019636.1\|WP_087541808.1\|4784095_4784704_-\|thermonuclease-family-protein	gnl\|CDD\|224442	COG1525, COG1525, Micrococcal nuclease (thermonuclease) homologs [DNA replication, recombination, and repair].	3.31887e-30
NZ_CP019636.1\|WP_087541797.1\|4764450_4764996_+\|NAD(P)H-dependent-oxidoreductase	gnl\|CDD\|223508	COG0431, COG0431, Predicted flavoprotein [General function prediction only].	6.1323e-45

>NZ_CP019636.1|WP_157679554.1|4771055_4771694_-|hypothetical-protein
MFNWLKTIFSAFLITLIITLHLSFTSPTPAYASTPFDFVSPKQLVKLLSNKLLVKDAKRFLEATPETICTAYFNKSAGIDSSTWKTIEEGATSAFTITHAIVSASTAGAGSLSGYAGIASAVSQLGLGSLTTAIAGMMGSSVTGAAATAVVTSAVGGPLVMSALLVGGTSATAFGTYELGKLAVERLGNWVESYCTSSSTSKSYEDVAITPH
>NZ_CP019636.1|WP_087541801.1|4769097_4770975_+|biosynthetic-type-acetolactate-synthase-large-subunit
MSLPQTESQSISNVFISPVVTPRRASGGFALLDSLKRHGVEHIFGYPGGAILPIYDDLYKVEAAGGGIKHILVRHEQGAAHAADGYARATGKVGVCFGTSGPGATNLVTGIATAYMDSIPMIVVTGQVPRHAIGTDAFQETDIYGITLPIIKHSYVVRDPADMARIVAEAFHIATTGRPGPVLIDVPKDVAFEEFDYVPVEPGRVRLPGYRPTVKGNPRQINAAIQLIRESRRPLLYVGGGAIAAGAHEEVKQLAELFNIPVTTTLMGIGAFDEHHPLALGMLGMHGTAYANFAVSDCDLLICVGARFDDRVTGKLDEFASRAKVIHIDIDPAEVGKNRVPEVPIVGDVRKVLIELLHRCQQTSAKNQPNQTQEWLNLINRWKEEYPLVVPQYPDSISPQEVIVELDRQAPNAIYTTDVGQHQMWAAQFLKNGPRRWISSAGLGTMGFGVPAAMGAKVAFPDQEVICISGDASFQMNLQELGTLAQYGINVKTVIINNGWQGMVRQWQQAFHGERYSCSNMEVGMPDIELLAKAYGIKGMVIQNRDELKDAIAEMLAHDGPVIVNVHVTKDENCYPMVAPGKSNAQMVGLPRQPKKASPEPIYCSNCGAKNPPNNNFCPECGTKL
>NZ_CP019636.1|WP_087541800.1|4767685_4768954_+|MFS-transporter
MFPTEPAAVNKGFIAVLKNRGFMLLWIGQLVSQLADKVFFVLMVALLENYPAPAGLAENSKYSTLMVAFTVPAILFGSAGGVFVDRFPKKLIMVGSDVVRGLLTLCIPFLPRDFLILLTLTFAISTVTQFFAPAEQAAIPLLVKKENLLAANALFSSTMMGALIVGFAVGEPILSLAKNFVGAEYGQELVVAGLYLLSAGIMQPINFRDNISLNNNQPVINPWTDFKEGLRYLKKNRLVLNAMLQLTTLYCVFAALTVLAIRLAAEFGLKEKQFGFFLAAAGVGMVLGAGILGHWGDKLHHKPLPLIGFLLMGLVLAVFSFTHNLLLAFVLCALLGIGAAFIGVPMQTLIQQQTPPTMHGKVFGFQNHAVNIALSAPLAITGPITDALGLRIVLVTMSVVVVSVGFWAWQNTRKVLQNIILK
>NZ_CP019636.1|WP_087541799.1|4766767_4767340_+|hypothetical-protein
MSIIICPGIHDSALTQCFLSVCQEQVIKRGKSHKAVNLQVFPAEGGLSLSAFHILQFLHKHFQDRIESPVVFISFSAGVVGSILAAHKWQQSGGRIKAFIAIDGWGVPLWGKFPIHRMSHDYFTHWSSSLLGSGENSFYADPPVEHLEMWGSPQTVQGYWVNSLYGESPPKEYLSAAEFLHLLLKRYGDN
>NZ_CP019636.1|WP_087541798.1|4765059_4766184_-|ferrochelatase
MVATPEKLQQTYEPLSVPGQNRVAVLLMGYGEVESYEDFANYNEQALNLLTAKFAPVPTWVYPPLARLLALFDRHEWGHQHHDFISPHNAIFEKQRAGIEKSLQEKWGEGVQVFKAFNFCAPFLPKQVLAEIKNQGFDKILIYPLLVVDSIFTSGIALEQVNNALAQMNEGDEHWVKGLRYIPSFYNESAYINLMAHLVEEKITTDLAGAYLPSQIGIVLMNHGCPHKAKGFTSGITESQILYDLVREELINRYPLISVGWLNHDTPLIEWTQPNAEQAAKNLIQLGAKAVIFMPIGFATENHETLLDVHHIIHALEKKYPDVNYVQMPCVNDHPEFLAMAAEWANAHIGELLSEQTVAVNPQLAVAHHHHHHH
>NZ_CP019636.1|WP_087541797.1|4764450_4764996_+|NAD(P)H-dependent-oxidoreductase
MVRIVGIGGSLRTESYTQQALGIAAQRVEALGADVEILDLRQLQLPFCNGEKEYPDFPDVQRMRDTVSRADALILATPEYHGGVSGVLKNALDLMSFEELSDKVVGLVSVLGGQPNSNALNDLRLIMRWVHAWVIPEQIGIGQVWKAFSPEGKLSDEKLSQRFDEFAQSLIDNTRKLRGVS
>NZ_CP019636.1|WP_087546262.1|4762102_4763980_-|ATP-dependent-zinc-metalloprotease-FtsH
MKQRPGKRAALTGALAAGLIMLPGMLGGTPALAQKVERDSLSYGELIKKTEKGEVKRVELDETEQVARVYLQGQKPDSQPLQVRLLEQNTELINRLKEKNVDFEEVSSANSRAAIGLLINLMWILPLVALMLLFLRRSTNASSQAMNFGKTRARFQMEAKTGVKFEDVAGIEEAKEELQEVVTFLKQPEKFTAVGARIPKGVLLVGPPGTGKTLLAKAIAGEAGVPFFSISGSEFVEMFVGVGASRVRDLFKKAKENAPCLIFIDEIDAVGRQRGAGIGGGNDEREQTLNQLLTEMDGFEGNTGIIIIAATNRPDVLDAALLRPGRFDRQVIVDAPDRKGRLEILKVHSRNKKVDPSVSLEVVARRTPGFTGADLANLLNEAAILTARRRKEAITQLEIDDAIDRLTIGLTLNPLLDSKKKRLIAYHEVGHALLSTLLKYADPLNKVTIIPRSGGVGGFSQQILNEEMIDSGLYTKAWLQDNITMTLGGKAAEVEVFGEAEVTGGASNDLKVVTNLARKMITMYGMSDLGLVALESQNSDVFLGRDWMSRSEYSEEMATKIDRQVRAMASTCYQEARRIIRENRALIDRLVDLLVEQETIEGEQFRKIVSEYTQLPEKQQLVVSG
>NZ_CP019636.1|WP_087546261.1|4761331_4762030_+|M23-family-metallopeptidase
MVEAVELNSKQITTLTNRSTTSFPVKNFQILQPKAAIEVKPQQIARANNWLAASFPVENFQSYTSAFGYRRSATGGSNVEFHSGLDIAAPQGSYIRNWWTGTVTKVSDGDACGTHIVIQSGEWEHTYCHMEGHVETAYGRRYLIDRAGGIQIAEGQQLGAGMRIGRVGMTGRTTGPHLHWGLKYAKQYVDPAMVLQEMFSQQQIARNSSQRWTSEQSQVIIEESKAIGDSGY
>NZ_CP019636.1|WP_087541796.1|4760295_4760685_-|hypothetical-protein
MLTEMLPFSFELDTIAIAGASLWSLALYLGFSPVSEWVIQQLNRWFNFAERSLYTSQSEFEKTKQARESQNAFYASLFSIVPFLVIGALLNWGVEISLGRSWAISMGILACIGCGVYELGRRDGESSGE
>NZ_CP019636.1|WP_087541795.1|4758755_4759985_+|calcium-binding-protein
MAVITGTPNNDNLSGTPDNDSINGLAGDDTLSGQAGNDEISGGEGKDFLDGNAGEDTLRGDPFLAPGSTANSTILALNRDGQDTLDGGSGNDFLEGGAGQDFLKGGEGNDILWGGYNTDEGLLTGNFSDVQEYQNNGYGNDVLEGGTGNDILRGDSIWVDPLFGLTTIAGDDRLDGGPGNDLLEGGPGSDYLEGGSGDDRIFTGYEVIQSSRQVANGNDTAYGGSGDDYIVGGTGNDLLNGDSGNDRLIGDSNGLYFGNDNLNGGFGDDILEGGYGSDLLDGGAGDDVLIGDVASPSPLSVNVIDVLIGGAGKDTFVLGTESGNLYDTSFSSSVSEYAIITDFKTNEDTIQLADSSPSGGALKYVLGSSPEGLPEGTGIYVDRPDTDVLVAIVQGVSGLSLDQSYFSFV
>NZ_CP019636.1|WP_087546263.1|4772191_4772839_-|GUN4-domain-containing-protein
MKENWISIHEATLDTNASKGHLPTLWLGLFFELGGGGVGWWLGGLLSKWSLSEDNLTSEKGVDYTKLRHLLAAGKWKEADNETYLVMLQAVGRQENDWIRKEELLTFPSTDLRTIDQLWVKYSNGHFGFSVQKQIYLSVGGKLRGEYYYVNSYEEAWKKFGDRVGWRVQGSWLTEYDVTFDSSAPEGHLPSQMLRMCFGEVWWVYLLSHRGLSSD
>NZ_CP019636.1|WP_087541804.1|4775581_4776979_-|hypothetical-protein
MRESVRTNKKQTSTADWRLTSGYLHEGRSDFESVHILLGRFLADRTSEAPLAEKELFSPDGIFEWGHASPLEKVIHSREDCEFLLKNPSLLRKSITIIEPWEYVGVNALGEDVRASKNIAYIAQKVADMDSVLLPVWSCGVIDPELVVPAITSGYAVIVEGGDPSVYDPSTWTSPACPREDMFALVEKLLISRSPASAPAIFICVGHQLAAECHIRLIRKAVKQVLSLTSLERDKNGRALKSLQEVAERIEAIGKTLKVKKRDGRLVASGWNDSHFAVTRNESKEVGDRVLLPYQSPDGETLGIPWEIIHAHDVTSDMHEGVIDTTIQYEHEVLISMFHSDEVNEEAILFANWAYRSIHDTIVPYRHVIAGSHLSWLIQLPDSVEILCSTAEENGEIVTECSATCINYKDFETKKIRRSFTCQFHPELLEDLRAIGSGEAPSYSTLKKDDGVRLFVRLLYAGMQE
>NZ_CP019636.1|WP_087546264.1|4777569_4779966_-|histidine-kinase
MTTVAIEKRVMTEEEVAKLWEAFKVFDADGSGAISTEELGQVMRSLGQSPSDIDLRDMIKEVDVDLSGSIDFEEFKTLLLSQQGDRKSRLKLAFSVFDEDGSRQITANELHNVMSLFGLTDEELEEMIKEVDHDGDASIDFEEFMKLVPEESELTTGYKDLPISFTSSPSSNATTVTAEIAATATNAPTITITESPVQETPSDNPEVARLKELLAQHPQEQKENATSRLQMQIGLFRLIQGAAYRSFRESFSANHETHLRVRNLPYKITDFVQFVQKAIELYKGLDVVEKACHPVLDAVVESIEKEYARLEDRIKNWNTIEKTPEMLAEDKAMQEARRKSTSVKEKFAAGVEFAITLKKKQFSFRDIAEGVLAINELNRLRQMELNAELAPPPPKSEGDPKDYLKRWNRVILSDASEEIPGAMMPVAYWYEDFMPKLLAAFSVNTAADIQSNTVPDEAALEQWYQQTKAVGEFDRYGADVAQNFSKCTPKQKLAVKQAWRLTHHYLNGVQKRRERQEFGRESGALSQYVAFLDVYLGRSDVQDSQMRVSFPYYIGPAVWRFFHTTAEIVSTKPHEEQKALVAVFKDFFKRFATMYPCPYCRHHLNMYVVQNKEVDMYPVEYLLLGRDPQLNNFEVSMEAKLSTVVDGPTLRLFFWKLHNTVSSSIARSEEWYHKDEKAFYTTRYWPSLDSELARSKALKHLSIAVERLYRLYGILKPASRLAGVRATLQKLLDKGDEEGIKEACTLAQDYIKELEEAAIAGQFLQETYRFDPEIVDKAPYFTPEEEEFARTGVFVEVI
>NZ_CP019636.1|WP_087541806.1|4780048_4781635_-|mechanosensitive-ion-channel-family-protein
MNIQIILAEVVFLILIFSLLNWLLGIMFRQLTRVSWLQGRTANITFLRRNLSRLLILICVVLCLALIGVNGLVIYRGGDLKEVQLNFVRSTPTQFWVNLCIASLKSVSLLILVKFSIPPLQRGIDWVCDYAKKADQIKANDDSIEAFFRTLKKTIINAIWIASAILCAKFFSLPEVVSKYLYIALKIYIIVTVGLLIVKAVATIVDTLDALSLKYSSSNNLLRLYERLRHLIPFFKKCLEYILYVGIVNLVVPEIEPIAWIGAYTPRIVQIIGIFFLSNVLIEVAYFILDEFYLKTIDLNDSQRQKRLTLIPLVRSFVKYFIYFTAGVTILKLIGIDPAPILAGAGIVGIAVGFGAQNLINDIVCGFLILFENYYLVGDYIQAGKTDERSVEGIVEAIELRTTHIRHPDGQLQIIRNGDIGSIISYSKQYIYARVEVSVSHNTNLDHVYRVIEKVGQQLKEDDQDVLEPTRVAGIEHFGEHNLRLLTLTKVKPGKHIHIQRVLRKILKETFNQEEIEIFGFPQESSSS
>NZ_CP019636.1|WP_087537548.1|4781922_4782801_-|IS982-family-transposase
MFSLDALFCHVDDFCKAFEAQWNKELLNHAGIRRIRAKSLCLSEIITILIAFHQNHYRNFKHFYLNQVKQQWSSAFPGLPSYQRFIEWIPSTLIPLCVYLKHCFGQCTGIGFIDSTSLKVCHNRRISRHKVFEGLAARGKTSVDWFFGFKLHLVVNELGQLLNVVLTPGNIDDRQPVPNLLNEMFGKIFGARGYVSQKLASQLLHEFGIQFFAKPRRNMKNKLMRLHDKLLSRKRSIIETINDQLKNISQIEHSRHRSPVNFCVNVLCGLIAYCHQPKKPSLQMDWLLSQTA
>NZ_CP019636.1|WP_087541807.1|4783062_4783749_-|hypothetical-protein
MSTFLSSVAVLLSTLALLCSGYTAYQVFTLQQTLNVASASNSSATTSTQKTSSVETSTASPDISPSPLETSSSTEKTTQSTTETETVSSPPKSKSTATSSTIKPGQFVQPAFGNKAEVELLSVKRIKDPATANRDVVNVQMRIRRLATDGISPEQSVAIFNTTARNPDTSETYKGVDIKRSTGSVGLFSLRPKASADAYVWLRIPDGVDKVDVFVPDTAAFSQVPISN
>NZ_CP019636.1|WP_087541808.1|4784095_4784704_-|thermonuclease-family-protein
MCFSLLSFHRKTLCFGIVKKTKQVLLWLCSAILIFGLIGCDRIFPSGDLVERVSDGDTLALKNAKGDKFTVRFACIDAPEIPHTKKEKQSKNSLALDQFDWGVKAQERVQQLVQQGGDRVKLNITDSDRYGRKVAEVRLRNGTFIQEVLVREGLALVYRPYLSKCPSKDIIQQAETQARDSRQGVWSDSKFVKPWEYRSLYK
>NZ_CP019636.1|WP_087541809.1|4785131_4785602_+|GNAT-family-N-acetyltransferase
MKIRIYEIDDTEEIMKLFYNTVHEVNIRDYTKEQVDAWAPTNMDIQVWIQGLKSKLTYVAEESHKILGFGELEENGHIDRFYCHKDFQGRGVGTQILEQIELKARSLGIKKLFTEASITAKPFFERKGFIVVRKQQVERRGQKFINFQMEKVLVSL
>NZ_CP019636.1|WP_087541810.1|4786249_4787359_-|Gfo/Idh/MocA-family-oxidoreductase
MNLAVIGVAVVGTGFGQKVHIPGFQAHPQTEVVAVYHRDLDKAQAIAASNNIPHACDTIADILRLEEVQAVSISTPPFLHYKMAKAVLQARKHVLLEKPTSLNAAEAKELYQLAQKAGVTAAVDFEFRFVPGWQLFFELLSEGYVGSKRLIRIDWLGSSRADAARPWNWYSRKDQGGGALGSLGSHTFDYIHWLFGPVRKLSAHFSTAINQRLDSNTGELKPVETDDTCMLMLELADGTPCQVSISAVVHASRTHWIEVYGDRGTLVLGSENQKDYIHGFHVWASQPGKPLAEIEIPNRLLFPKNHSDGRISAFIRVIDQWVQGIESKEEIVPSLREGVYSQLLMDLSHQSNNTSSWVDVPSLETFLAD
>NZ_CP019636.1|WP_087541811.1|4787483_4787951_-|DUF4870-domain-containing-protein
MRENPKQQIRMWAMLCHLSALLWLPLVSLLFLGIPLYLPFLNILGPLIIWHSRKKYDPWIDFQGKESLNFQLSLTVYALIVIFVSLLMVFATCGVAVTTYLSAKHMATIFNSLIAVLSLFISALMLSQLIFVNFAAIRAYKGQYYRYPFTIRFLR

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Crispr_ID: NZ_CP019636_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_13

4907538-4909027

TypeIII

Consensus_repeat	Method
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	PILER-CR
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CRISPRCasFinder
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CRT

20 spacers

cas6,csx1,csx21,csm3gr7,csx19,PD-DExK

The CRISPR arrays of NZ_CP019636_13

>merge|NZ_CP019636|13|4907538-4909027|PILER-CR,CRISPRCasFinder,CRT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCACCTTGTAATAGAGCTTGAGAACTATCACCGTAACTAGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTCATCATTTCAGTGTAAACGAACAAAAAAGCCTGCGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTTTGAACGGATTAAGTGTGTAGTGCGTCTTTTTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACGTATCAAGGGTGATGAACGCTTTGGCTACGTTCAGGTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACGAACCAGCCGTGCAGAGATGTACGGCTTTCCCATGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCTTGCTGCCGCTAGCGACGAGCTAAGCAGAAGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACAGAGCAAAAATAGGAAGTACGTAAAATCAATGGTTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCCTTGCGCTCTTCAGGGAACGGGTTTTTGGGAAGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACAGAAACTTACACTGGTCAGGTGTTGATTCCAAAGAAGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTTGATAACCATAAATAAGTCATTTCTCTCATCAAAACGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCTAGATAGGATGGAACTTGTACAGAAGCATCACCAAGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCTTAACCTGGCTAGCTTAACACCCACTTCGCGTAGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACACTGTAATACTTGTCGCGTTTGCCACAGCACTAGTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACGTCCTTGGTGTCACTCCATCCGTTGCCGTCCACAGTCTGGCGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACGGAAATGACCCAACTTTTTTATCAGTGTCTAGTTGCGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCATTCCTCAAGCACCCTCTCCCGCGTAGACCTGTGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACATGAGAAGTTTTATCTTTCCTATTCGACACTGGGTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCTCGTTCGAGCATGGATGGGATAGTACGGCAAGTATTTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTTTAGAAAACAACGCTTTAGATAAAATGGACTCAAGTGACAAATTACCTCTTCCCTGTAAGGGGACGGAAATATGAAGGGTCTACCGAGAGCTGTCGCTAGAGGGTAACTTTTCCTAATCACTTCCCCGCAAGGGGATTGAAAC

>NZ_CP019636|13|4|4907538-4908808|PILER-CR
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CACCTTGTAATAGAGCTTGAGAACTATCACCGTAACTAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TCATCATTTCAGTGTAAACGAACAAAAAAGCCTGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTTGAACGGATTAAGTGTGTAGTGCGTCTTTTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GTATCAAGGGTGATGAACGCTTTGGCTACGTTCAGGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GAACCAGCCGTGCAGAGATGTACGGCTTTCCCAT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTGCTGCCGCTAGCGACGAGCTAAGCAGAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGAGCAAAAATAGGAAGTACGTAAAATCAATGGTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CCTTGCGCTCTTCAGGGAACGGGTTTTTGGGAAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGAAACTTACACTGGTCAGGTGTTGATTCCAAAGAAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTGATAACCATAAATAAGTCATTTCTCTCATCAAAAC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTAGATAGGATGGAACTTGTACAGAAGCATCACCAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTAACCTGGCTAGCTTAACACCCACTTCGCGTAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ACTGTAATACTTGTCGCGTTTGCCACAGCACTAGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GTCCTTGGTGTCACTCCATCCGTTGCCGTCCACAGTCTGGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GGAAATGACCCAACTTTTTTATCAGTGTCTAGTTGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CATTCCTCAAGCACCCTCTCCCGCGTAGACCTGTG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ATGAGAAGTTTTATCTTTCCTATTCGACACTGGGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC

>NZ_CP019636|13|13|4907538-4909027|CRISPRCasFinder
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CACCTTGTAATAGAGCTTGAGAACTATCACCGTAACTAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TCATCATTTCAGTGTAAACGAACAAAAAAGCCTGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTTGAACGGATTAAGTGTGTAGTGCGTCTTTTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GTATCAAGGGTGATGAACGCTTTGGCTACGTTCAGGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GAACCAGCCGTGCAGAGATGTACGGCTTTCCCAT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTGCTGCCGCTAGCGACGAGCTAAGCAGAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGAGCAAAAATAGGAAGTACGTAAAATCAATGGTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CCTTGCGCTCTTCAGGGAACGGGTTTTTGGGAAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGAAACTTACACTGGTCAGGTGTTGATTCCAAAGAAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTGATAACCATAAATAAGTCATTTCTCTCATCAAAAC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTAGATAGGATGGAACTTGTACAGAAGCATCACCAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTAACCTGGCTAGCTTAACACCCACTTCGCGTAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ACTGTAATACTTGTCGCGTTTGCCACAGCACTAGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GTCCTTGGTGTCACTCCATCCGTTGCCGTCCACAGTCTGGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GGAAATGACCCAACTTTTTTATCAGTGTCTAGTTGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CATTCCTCAAGCACCCTCTCCCGCGTAGACCTGTG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ATGAGAAGTTTTATCTTTCCTATTCGACACTGGGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTCGTTCGAGCATGGATGGGATAGTACGGCAAGTATTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTTAGAAAACAACGCTTTAGATAAAATGGACTCAA
GTGACAAATTACCTCTTCCCTGTAAGGGGACGGAAAT	ATGAAGGGTCTACCGAGAGCTGTCGCTAGAGGGTA
ACTTTTCCTAATCACTTCCCCGCAAGGGGATTGAAAC

>NZ_CP019636|13|4|4907538-4908955|CRT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CACCTTGTAATAGAGCTTGAGAACTATCACCGTAACTAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TCATCATTTCAGTGTAAACGAACAAAAAAGCCTGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTTGAACGGATTAAGTGTGTAGTGCGTCTTTTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GTATCAAGGGTGATGAACGCTTTGGCTACGTTCAGGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GAACCAGCCGTGCAGAGATGTACGGCTTTCCCAT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTGCTGCCGCTAGCGACGAGCTAAGCAGAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGAGCAAAAATAGGAAGTACGTAAAATCAATGGTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CCTTGCGCTCTTCAGGGAACGGGTTTTTGGGAAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGAAACTTACACTGGTCAGGTGTTGATTCCAAAGAAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTGATAACCATAAATAAGTCATTTCTCTCATCAAAAC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTAGATAGGATGGAACTTGTACAGAAGCATCACCAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTAACCTGGCTAGCTTAACACCCACTTCGCGTAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ACTGTAATACTTGTCGCGTTTGCCACAGCACTAGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GTCCTTGGTGTCACTCCATCCGTTGCCGTCCACAGTCTGGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	GGAAATGACCCAACTTTTTTATCAGTGTCTAGTTGC
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CATTCCTCAAGCACCCTCTCCCGCGTAGACCTGTG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ATGAGAAGTTTTATCTTTCCTATTCGACACTGGGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTCGTTCGAGCATGGATGGGATAGTACGGCAAGTATTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTTAGAAAACAACGCTTTAGATAAAATGGACTCAA
GTGACAAATTACCTCTTCCCTGTAAGGGGACGGAAAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087541901.1\|4913140_4914154_-\|CRISPR-associated-protein	csm3gr7	COG1337_csm3gr7_CAS-III-D	gnl\|CDD\|224256
NZ_CP019636.1\|WP_087541890.1\|4899066_4900602_-\|nitrogenase-molybdenum-iron-protein-subunit-beta	unknown	unknown	gnl\|CDD\|130353
NZ_CP019636.1\|WP_087541903.1\|4914806_4915613_-\|CRISPR-associated-RAMP-protein	csm3gr7	cd09683_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|187814
NZ_CP019636.1\|WP_087546015.1\|4917605_4918676_+\|transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP019636.1\|WP_087541902.1\|4914184_4914805_-\|hypothetical-protein	PD-DExK	mkCas0061_PD-DExK_CAS-I:CAS-III	unknown
NZ_CP019636.1\|WP_087546272.1\|4906410_4906674_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541893.1\|4904570_4905110_-\|DUF2267-domain-containing-protein	unknown	unknown	gnl\|CDD\|227789
NZ_CP019636.1\|WP_087541896.1\|4909070_4910186_+\|CRISPR-associated-endoribonuclease-Cas6	cas6	COG5551_cas6_CAS-III	gnl\|CDD\|227838
NZ_CP019636.1\|WP_087541892.1\|4902965_4904066_+\|isopenicillin-N-synthase-family-oxygenase	unknown	unknown	gnl\|CDD\|226022
NZ_CP019636.1\|WP_087541900.1\|4912583_4913144_-\|hypothetical-protein	csx19	cls000059_csx19_CAS-III-D	unknown
NZ_CP019636.1\|WP_087541898.1\|4910899_4911544_-\|hypothetical-protein	csx21	mkCas0116_csx21_CAS-III-A:CAS-III-D	unknown
NZ_CP019636.1\|WP_087541894.1\|4905447_4905930_-\|DUF3368-domain-containing-protein	unknown	unknown	gnl\|CDD\|225269
NZ_CP019636.1\|WP_087541897.1\|4910214_4910721_-\|hypothetical-protein	csx1	pfam09670_csx1_CAS-III	gnl\|CDD\|187878
NZ_CP019636.1\|WP_087541891.1\|4900786_4900882_-\|nitrogenase-molybdenum-iron-protein-subunit-alpha	unknown	unknown	gnl\|CDD\|162284
NZ_CP019636.1\|WP_157679564.1\|4905232_4905394_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541899.1\|4911546_4912587_-\|CRISPR-associated-protein	csm3gr7	cls000253_csm3gr7_CAS-III-A:CAS-III-D	gnl\|CDD\|274902
NZ_CP019636.1\|WP_087541895.1\|4906203_4906383_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546270.1\|4901172_4902474_+\|integrase	unknown	unknown	gnl\|CDD\|271177
NZ_CP019636.1\|WP_087546271.1\|4905913_4906168_-\|UPF0175-family-protein	unknown	unknown	gnl\|CDD\|377095
NZ_CP019636.1\|WP_087546013.1\|4915587_4916967_-\|IS110-family-transposase	unknown	unknown	gnl\|CDD\|376564

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087541901.1\|4913140_4914154_-\|CRISPR-associated-protein	gnl\|CDD\|224256	COG1337, COG1337, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	5.48813e-44
NZ_CP019636.1\|WP_087541890.1\|4899066_4900602_-\|nitrogenase-molybdenum-iron-protein-subunit-beta	gnl\|CDD\|130353	TIGR01286, Nitrogenase_molybdenum-iron_protein_beta_chain, nitrogenase molybdenum-iron protein beta chain. This model represents the majority of known sequences of the nitrogenase molybdenum-iron protein beta subunit. A distinct clade in a phylogenetic tree contains molybdenum-iron, vanadium-iron, and iron-iron forms of nitrogenase beta subunit and is excluded from this model. Nitrogenase, also called dinitrogenase, is responsible for nitrogen fixation. Note: the trusted cutoff score has recently been lowered to include an additional family in which the beta subunit is shorter by about 50 amino acids at the N-terminus. In species with the shorter form of the beta subunit, the alpha subunit has a novel insert of similar length. [Central intermediary metabolism, Nitrogen fixation].	0
NZ_CP019636.1\|WP_087541903.1\|4914806_4915613_-\|CRISPR-associated-RAMP-protein	gnl\|CDD\|187814	cd09683, Csm3_III-A, CRISPR/Cas system-associated RAMP superfamily protein Csm3. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; RAMP superfamily protein.	4.17865e-71
NZ_CP019636.1\|WP_087541893.1\|4904570_4905110_-\|DUF2267-domain-containing-protein	gnl\|CDD\|227789	COG5502, COG5502, Uncharacterized conserved protein [Function unknown].	4.79149e-33
NZ_CP019636.1\|WP_087541896.1\|4909070_4910186_+\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|227838	COG5551, COG5551, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	4.82467e-39
NZ_CP019636.1\|WP_087541892.1\|4902965_4904066_+\|isopenicillin-N-synthase-family-oxygenase	gnl\|CDD\|226022	COG3491, PcbC, Isopenicillin N synthase and related dioxygenases [General function prediction only].	8.17447e-51
NZ_CP019636.1\|WP_087541894.1\|4905447_4905930_-\|DUF3368-domain-containing-protein	gnl\|CDD\|225269	COG2405, COG2405, Predicted nucleic acid-binding protein, contains PIN domain [General function prediction only].	6.03679e-42
NZ_CP019636.1\|WP_087546015.1\|4917605_4918676_+\|transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	4.11208e-07
NZ_CP019636.1\|WP_087541891.1\|4900786_4900882_-\|nitrogenase-molybdenum-iron-protein-subunit-alpha	gnl\|CDD\|162284	TIGR01282, Nitrogenase_molybdenum-iron_protein_alpha_chain, nitrogenase molybdenum-iron protein alpha chain. Nitrogenase consists of alpha (NifD) and beta (NifK) subunits of the molybdenum-iron protein and an ATP-binding iron-sulfur protein (NifH). This model describes a large clade of NifD proteins, but excludes a lineage that contains putative NifD and NifD homologs from species with vanadium-dependent nitrogenases. [Central intermediary metabolism, Nitrogen fixation].	9.56676e-07
NZ_CP019636.1\|WP_087546271.1\|4905913_4906168_-\|UPF0175-family-protein	gnl\|CDD\|377095	pfam03683, UPF0175, Uncharacterized protein family (UPF0175). This family contains small proteins of unknown function.	6.50679e-22
NZ_CP019636.1\|WP_087541899.1\|4911546_4912587_-\|CRISPR-associated-protein	gnl\|CDD\|274902	TIGR03986, CRISPR-associated_protein, CRISPR-associated protein. Members of this protein family, part of the larger RAMP family, are found exclusively in species with CRISPR systems, in local contexts containing other RAMP (Repeat-Associated Mystery Proteins).	1.22214e-17
NZ_CP019636.1\|WP_087546270.1\|4901172_4902474_+\|integrase	gnl\|CDD\|271177	cd00796, INT_Rci_Hp1_C, Shufflon-specific DNA recombinase Rci and Bacteriophage Hp1_like integrase, C-terminal catalytic domain. Rci protein is a tyrosine recombinase specifically involved in Shufflon type of DNA rearrangement in bacteria. The shufflon of plasmid R64 consists of four invertible DNA segments which are separated and flanked by seven 19-bp repeat sequences. RCI recombinase facilitates the site-specific recombination between any inverted repeats results in an inversion of the DNA segment(s) either independently or in groups. HP1 integrase promotes site-specific recombination of the HP1 genome into that of Haemophilus influenza. Bacteriophage Hp1_like integrases are tyrosine based site specific recombinases. They belong to the superfamily of DNA breaking-rejoining enzymes, which share the same fold in their catalytic domain and the overall reaction mechanism. The catalytic domain contains six conserved active site residues. Their overall reaction mechanism is essentially identical and involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA.	4.69533e-31
NZ_CP019636.1\|WP_087541897.1\|4910214_4910721_-\|hypothetical-protein	gnl\|CDD\|187878	cd09747, Csx1_III-U, CRISPR/Cas system-associated protein Csx1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Protein of this family often fused to HTH domain; Some proteins could have an additional fusion with RecB-family nuclease domain; Core domain appears to have a Rossmann-like fold; loosely associated with CRISPR/Cas systems; also known as Cas02710 family.	2.20643e-18
NZ_CP019636.1\|WP_087546013.1\|4915587_4916967_-\|IS110-family-transposase	gnl\|CDD\|376564	pfam01548, DEDD_Tnp_IS110, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family includes an amino-terminal region of the pilin gene inverting protein (PIVML) and of members of the IS111A/IS1328/IS1533 family of transposases. The C-terminus is represented by family pfam02371.	7.7599e-20

>NZ_CP019636.1|WP_087546272.1|4906410_4906674_-|hypothetical-protein
MGVQLVRPRPHSSKQHKPKFQSKLPGWSRTYVTDPKNRQLQRVLKGMLHYDISTARRLLKQQRQLHPGQSDNWYLEKVIHDLERDRH
>NZ_CP019636.1|WP_087541895.1|4906203_4906383_-|hypothetical-protein
MDQDTWIYTNKRPGNLVLRFRVKGFEKQFFVGTSLADKLRNRELVGVRRVRTVECLSIA
>NZ_CP019636.1|WP_087546271.1|4905913_4906168_-|UPF0175-family-protein
MGLQISISDSIVQALRLPEQRVEQELRQELAIALYTQNILPFGKARELAEMDKYEFGQLLARRGVVRHYGLEELNDDLNYARGE
>NZ_CP019636.1|WP_087541894.1|4905447_4905930_-|DUF3368-domain-containing-protein
MLVVSNTSPILNLAIINQLILLHQQFGEVLIPSAVLDELKISEERPGSQAIREAISTGWIQSREVSNEPLSQLLKQTLDKGESEAIALAIELKADWTLLDEREGRKVAKSLGLRVTGILGVLLRAKQSGELKSLQPVIDELISRAGFRIAPELLVQILTQ
>NZ_CP019636.1|WP_157679564.1|4905232_4905394_+|hypothetical-protein
MISNFLRQLPEPNLMPQEEHPLAKFAGVLSDSEARELQKAIAAEFEQVDIDEW
>NZ_CP019636.1|WP_087541893.1|4904570_4905110_-|DUF2267-domain-containing-protein
MPDQTFRQNLPEVDPTEIEDSRTAIADEHRSFLEKVLVKGGFADLYDARDFTEVVFRVMRDLMTTEASDRVAAELHKEAVPTEEKALQMEVSDLWKDTNPIVGFLSRVRPPWQGPGIFKIDSDRFLFRVANEGGLPPTVEREQAVKAVFSATKDELSEERIQEIASWLPDHVRELWEQA
>NZ_CP019636.1|WP_087541892.1|4902965_4904066_+|isopenicillin-N-synthase-family-oxygenase
MGAYLEESKDFVKNMQALTTRSFETFDVRAPKNLKEQRELGERIVAALQRDSLIQIQKNYQEDLLTAQALLQNRKFNQLPFDGKIKFVSDTTYTGYVFSGEEKKGGQYDQVEVYTVFPHFDKDDELVKTLRLPCHGEAVYPSVEYKNAIEAYMKATGNMCDQLIEIIGLGLGLEPNHYLSKMVRDGFHHARVLRFKSQKEAGGSSNGISAHSDYGFLIAASQDDVGGLWVRPITNGEKRGRNYLEEETTIGAYNDQPGWAFVTPTASVWTVFVGDMMELATDRKLKANLHKVILNEEKERFAIAYFHEPKFNQTFLSVNSKGQKKEIVYGKHLTNMYTKAYPNRSTTKRIESEELIKNIDRLPKIS
>NZ_CP019636.1|WP_087546270.1|4901172_4902474_+|integrase
MRTKVLQELEKVNQRLKSAKTKVTIRESNGSLQLRATLPLKPGDKDNNGTARKQYNISLNIPANLDGLKTAEEEAYELGKLIARKTFEWNDKYLGSEAIKKDFKTIGELLEQFEDEYFKTHKRTTKSEHTFFYYFSRTKRFTNPQDLATSDNLISSIEKVDKEWAKYNAARAISAFCLTFKIEIDLSKYSKMPENNSRNIPTDSEICAGILKFEDYLNTRGNQVNQNVQDSWQLWRWAYGMLAVFGLRPRELFINPDINWWLSQENADLTWKVHKDCKTGEREALPLHKQWIEDFDLRNPKYLEMLATAISKKDSTNHADITALTQRVSWWFRKIGLNFKPYDLRHAWAIRAHILGIPIKAAADNLGHSMQVHTQTYQRWFSLDMRKLAMNQALTKKNEIEFIKEENAKLKMENEKLKLEIEKLKMELVYKRN
>NZ_CP019636.1|WP_087541891.1|4900786_4900882_-|nitrogenase-molybdenum-iron-protein-subunit-alpha
MDLALNSPTWGLIGAPWNKNAKAKAGAKAIA
>NZ_CP019636.1|WP_087541890.1|4899066_4900602_-|nitrogenase-molybdenum-iron-protein-subunit-beta
MPQNPEKIQDHVELFHQPEYQELFENKKQFENGHDPEEVKRVAEWTKTWEYREKNFAREALTVNPAKGCQPLGAIFAAVGFEGTLPFVQGSQGCVAYFRTHLTRHYKEPFSGVSSSMTEDAAVFGGLQNMIDGLANSYQLYKPKMIAVCTTCMAEVIGDDLGAFITNAKNAGSVPENFPVPFAHTPSFVGSHITGYDNMMKGILSNLTAGKKKETSNGKINFIPGFDTYVGNNREIKRICNLMGIDYTILADNSDYLDSPNTGEFDMYPGGTPLEEAADSINAKATVALQAHSTPKTRDYIAKEWKQEVVVSRPWGIKGTDEFLVKLSELTGKPIPEELEIERGRAVDAMTDSHAWVHGKRFAIYGDPDLVYSVVGFMLEMGAEPVHILVHNSNDEFEKELKQLLESSPFGKSATIWPGKDLWHLRSLLFTEPVDLLIGNSYGKYLWRDCKVPLVRIGYPIMDRHHLHRYSTIGYQGVINLLNWVVNTIFEEIDHNTNIPSKTDISYDLIR
>NZ_CP019636.1|WP_087541896.1|4909070_4910186_+|CRISPR-associated-endoribonuclease-Cas6
MPRRISKQPKSQERNLIWSPETELVGLVFELVSQADASVYPQYTIGLHAWFLDQVRSSDPELSAYLHDGESEKPFTISALDGEMVSSGREVQLKANTSYYWYVTALSSRVVQWMSQWVQNLPKELNLRDASLQIRSCQIALPATTYAQLLNSEHGETITLKFLSPTSFRRKGHHFPLPMPTNVFHSYLRRWNDFSGIPVDQEAFLDFIDENVLITRHQLTSTKVLAGKKGAVTGFTGAIEFALTKKAFEQTEFCKLLYALGKLAPYCGTGHKTTFGLGQTRLGWSSQVAPEMPDVQSLLARRIEELTDIFKAQRKRTGGDRAEETATKWATILARREMGESLQVVAQELEMPYETVKTYVKLARRALKNPG
>NZ_CP019636.1|WP_087541897.1|4910214_4910721_-|hypothetical-protein
MPKTLLVTVGGSFQPIVTAIYSLQPDRVIFIASDGDKGSKSQVIGEGTPCEVRRGSEVIERLPNIPTQVDLGERFQPQRDLVLIQNPDNLSECYLKIQRCIHHLQQETPDHEILADYTGGTKTLSAALVLAAVDCGISLYLTIASTRENLVKVERGELTQPVDTSFRC
>NZ_CP019636.1|WP_087541898.1|4910899_4911544_-|hypothetical-protein
MTMVESSSESLTDAEWEIAHVIAQTLVKEDTDVNELGKAVAYLRTVVDKPDPTSRFFKYLKTLVSNGRQIGHSNRTSDYYRSIEKACSDYLKGVGDAYRILQILGWVSRLMRYYKDAGVPIGETTISTPSPVESSRQVEIAKVVRSHDFQVDQILEAIVTKINGNKVTYEILGTIKLTEKEPKKASVLKERQMVQVKIVSLKEDGSIKSIKCIS
>NZ_CP019636.1|WP_087541899.1|4911546_4912587_-|CRISPR-associated-protein
MTGNRPQRPHRVDSSPELAPKPYEFVSFPKERPNLQRPVGHHKYLSDRLHGALYLKLKVQTSLHVSTGVVVMGNDIGSRIPLIKTMVQDVDQKLSIGGSSLKGCIRSVYEAITNSTLAVITSKYRSQIPTERLPCRNKEQLCPASRVFGALDWQGLLDFNDAKCENMGFATGFMPSLYRPRPEERSAYFIRGQVAGRKFYYHTIRAIDKGQNAGIPVQQAAREYTFTTVLHFKNLLAEELGTLFIALGQDPKYPIALKVGGGKPIGMGTMTVTVEKMLQAQKLQLQQRYSSYNLNESDELVGKKLQQFIHEKIQAAHSRLIQKPQLEELTAVLRYPTDREPPSGMY
>NZ_CP019636.1|WP_087541900.1|4912583_4913144_-|hypothetical-protein
MKPFVGYKKEPLSVPQLLELIPKLVIEPNYYFFRWTHKVSGIVEKTPTHDEFPMIEGQMFNHNCELRWKYKCQNTYEVLLLSIGDKHDDFIPVKETINKEEKEPWRIEPNNPPYAYPAYGYRPDTTRFPKKLIFPDTLDIRLQEEIKEEEIKEEKNNKPKLAQRYFIDNESSTVQFVALTVELAQT
>NZ_CP019636.1|WP_087541901.1|4913140_4914154_-|CRISPR-associated-protein
MHKRFVNHCTIDITLIPDGPILIKSGKEGADPTKPDMEFVETYHAGGRSIYLPGSSLKGAIRAHAERIVRTIGSEKRPPENTQKLWSSNLLDERDKQNNPNFYLEDWKNREKKKKLEERHPHLGAELYKQSCFISQIFGNTSIASRVRIEDAYPEKSQPLKIEERNGVAIDRVFGSVAVGPFNYQVCTAGEFRTKIHLKNFTLAQLGLIGLVLRDLDDGWFGLGFAKSRGLGTVQVKLNKAVVQYPGCILSEDEQQIRALGSEKKWSKTFLLGAGEFLEPQEAQSYGFPTQDRQDTPAAAQEMDLGFGVQLTWREGTVKDLFERSVKSWSYLLVEAK
>NZ_CP019636.1|WP_087541902.1|4914184_4914805_-|hypothetical-protein
MAFSSYKAIGEVLKAFQVIYTEANFVGEVEFKIPDYFREDLETMMRDGVVDNSEFAICENLIYPVLKEVWKCYRSKFILWSHQSLNYDEKLSGFPEYILAKRSPLGKVVFDKPYFILVEAKQDNFEAAWAQCLAEMIAAQRLNAELPITIFGMTSNGDRWQFGKLEGEVFTRNITFYTIQELDKLFAAVNYIFQQCELQLNNLVAA
>NZ_CP019636.1|WP_087541903.1|4914806_4915613_-|CRISPR-associated-RAMP-protein
MTQRNVFLESLPVIKDAFGNPLIPGSSFKGAMRSRLESFLRGIMGSDRKLVANPANEYEWSITSQEMKQLKENHDNDEVLTAEIIKHTDIASHLFGSPWLASKFQVRDLTVVPDTWFGQYQERDGVAIDRDTETAADGKLYDFQVVPAGTQFKFQAVVENAEEWALGLLMIGLHQFETEQIPLGGGRSRGLGVVRLEIDKMQWVDVTDERDPNKTDPNKLLKYLRKLVDNESAYTDAKPLKSKWAKALINHLEQKISHSSTESISSGG
>NZ_CP019636.1|WP_087546013.1|4915587_4916967_-|IS110-family-transposase
MKKQEQPIAAEQRNLPVINPNAAGIDIGADRHWVSVPVDRDSENVHSFACFTAELYAMADWLKQCGIETVAMESTGVYWIPVFQVLESRGFEVKLVNAHYVKTVPGRKTDVLDCQWLQKLHSYGLLSGSFRPDDQICVLRSYIRQRDNLIKSACVHVQRMQKALTEMNLQLHRVISDITGTTGLSIIKAIVRGERNPLTLAALKDGRIKASCEEIAAALTGDYRDELIFILQQELQLYEFYQTQILAVDAQIEQCLASFADRVDVTKKPLTKPKRRGKKQPGNAPQFDLRTHLYRISGVDFTQIQGFGALTVLILLSELGLDPTRFPTVKHFTSWLGLCPGSRVTGGKVKSSQTRSVVSRAANAFRMAAQTLCRSNSALGAYYRRMQAKIGAPKAITAAAHKLARIFYRLWTSGDKFIDPGVDAYEQQYRERVVNNLKKKALTFGLELIPISDSTQCVS
>NZ_CP019636.1|WP_087546015.1|4917605_4918676_+|transposase
MPTQYQKDNLDTMMGLFLEAQGHPLPEHSQTKSPSALSRFLNMNPWSTKDMIRIVRSHVLETVSKVLSASGKGRRPFLQVIIDLTTLEKRGKFKEFEDLIRVYNGKRGLHIVVVYLVVGKWRIPWNFRVWRGKGTPSPAQLGLKLVKRLPKYLTERFQVIILADTAFGSVEFLDGVRKFRYHAVTGVAINRKLVDGRVLRHLHKQGQQVHLVGLKFPVTVSWYYLKRDKGKLEKRFVLSTRPIKASTLKWWGKRRWQIEGWFKTAKHRFGLHRFGQGSLLGMYRWLILSLTAYLIAHWTYLHIQSASPPDWGQAAQTALESIFPQIVVSLLLLNIERLAPLARSCGFDIHISRCKM

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Crispr_ID: NZ_CP019636_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_15

4932041-4932518

TypeIII

Consensus_repeat	Method
GTTGCTTAACCACTAATCCCCGCAAGGGGACTGAAAC	PILER-CR
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	CRT

6 spacers

WYL,csx3,cas10,csm3gr7,csx10gr5,csm2gr11

The CRISPR arrays of NZ_CP019636_15

>merge|NZ_CP019636|15|4932041-4932518|PILER-CR,CRT
GTTTTAGTCCCCTTGCGGGGATTAGTAGTTAAGCAACCTTCTTGGTCTTCCCAATCTTTCCCGAAGGAATGCCGGTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAACTCCATATTTTCTCCTTTTGTCTTCATTTTTATTAGTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAACCCCGAATCTCCGCCAAATCTTCCCAGCTAAGTAAGGTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAACTTCTCTGTAATATTGAGCTAGACAAGAGTGTAAGGGAAAGTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAACGTCATGAGGTGGTCACTAACTGGTATGGTTCTCAAGTTCGTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAACCTAAGTCTAAGCGGTCGATGAATGCCGCTATGATGGTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC

>NZ_CP019636|15|6|4932041-4932518|PILER-CR
GTTTTAGTCCCCTTGCGGGGATTAGTAGTTAAGCAAC	CTTCTTGGTCTTCCCAATCTTTCCCGAAGGAATGCCG
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	TCCATATTTTCTCCTTTTGTCTTCATTTTTATTA
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	CCCGAATCTCCGCCAAATCTTCCCAGCTAAGTAAG
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	TTCTCTGTAATATTGAGCTAGACAAGAGTGTAAGGGAAA
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	GTCATGAGGTGGTCACTAACTGGTATGGTTCTCAAGTTC
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	CTAAGTCTAAGCGGTCGATGAATGCCGCTATGATG
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC

>NZ_CP019636|15|6|4932041-4932518|CRT
GTTTTAGTCCCCTTGCGGGGATTAGTAGTTAAGCAAC	CTTCTTGGTCTTCCCAATCTTTCCCGAAGGAATGCCG
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	TCCATATTTTCTCCTTTTGTCTTCATTTTTATTA
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	CCCGAATCTCCGCCAAATCTTCCCAGCTAAGTAAG
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	TTCTCTGTAATATTGAGCTAGACAAGAGTGTAAGGGAAA
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	GTCATGAGGTGGTCACTAACTGGTATGGTTCTCAAGTTC
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC	CTAAGTCTAAGCGGTCGATGAATGCCGCTATGATG
GTTTCAGTCCCCTTGCGGGGATTAGTGGTTAAGCAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087541914.1\|4934078_4936319_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_157679566.1\|4930221_4930413_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541918.1\|4938263_4939331_+\|zinc-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|376518
NZ_CP019636.1\|WP_087546274.1\|4930661_4932029_+\|TIGR03985-family-CRISPR-associated-protein	WYL	mkCas0075_WYL_CAS-I:CAS-III	gnl\|CDD\|274901
NZ_CP019636.1\|WP_087546273.1\|4928518_4929445_-\|CRISPR-associated-protein-Csx3	csx3	mkCas0115_csx3_CAS-I:CAS-III	gnl\|CDD\|370583
NZ_CP019636.1\|WP_087541908.1\|4924071_4926414_-\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl\|CDD\|274208
NZ_CP019636.1\|WP_087541907.1\|4923367_4924075_-\|CRISPR-associated-protein-Csm3	csm3gr7	COG1337_csm3gr7_CAS-III-D	gnl\|CDD\|224256
NZ_CP019636.1\|WP_087541919.1\|4943936_4944797_+\|metal-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224033
NZ_CP019636.1\|WP_087541909.1\|4926814_4927159_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541906.1\|4922114_4923371_-\|CRISPR-associated-RAMP-protein-Csx10	csx10gr5	cd09700_csx10gr5_CAS-III-D	gnl\|CDD\|131722
NZ_CP019636.1\|WP_087541911.1\|4927596_4928451_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|187833
NZ_CP019636.1\|WP_087541917.1\|4937615_4937924_-\|metal-sensitive-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197393
NZ_CP019636.1\|WP_087541910.1\|4927151_4927574_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538406.1\|4942718_4943282_-\|recombinase-family-protein	unknown	unknown	gnl\|CDD\|239737
NZ_CP019636.1\|WP_087541915.1\|4936585_4936828_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538405.1\|4940102_4941074_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|225806
NZ_CP019636.1\|WP_087541920.1\|4946941_4949737_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541916.1\|4936947_4937130_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541913.1\|4933653_4934070_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541905.1\|4921707_4922118_-\|hypothetical-protein	csm2gr11	mkCas0063_csm2gr11_CAS-III-D	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087538406.1\|4942718_4943282_-\|recombinase-family-protein	gnl\|CDD\|239737	cd03768, SR_ResInv, Serine Recombinase (SR) family, Resolvase and Invertase subfamily, catalytic domain; members contain a C-terminal DNA binding domain. Serine recombinases catalyze site-specific recombination of DNA molecules by a concerted, four-strand cleavage and rejoining mechanism which involves a transient phosphoserine linkage between DNA and the enzyme. They are functionally versatile and include resolvases, invertases, integrases, and transposases. Resolvases and invertases affect resolution or inversion and comprise a major phylogenic group. Resolvases (e.g. Tn3, gamma-delta, and Tn5044) normally recombine two sites in direct repeat causing deletion of the DNA between the sites. Invertases (e.g. Gin and Hin) recombine sites in inverted repeat to invert the DNA between the sites. Cointegrate resolution with gamma-delta resolvase requires the formation of a synaptosome of three resolvase dimers bound to each of two res sites on the DNA. Also included in this subfamily are some putative integrases including a sequence from bacteriophage phi-FC1.	1.3966e-60
NZ_CP019636.1\|WP_087541919.1\|4943936_4944797_+\|metal-ABC-transporter-permease	gnl\|CDD\|224033	COG1108, ZnuB, ABC-type Mn2+/Zn2+ transport systems, permease components [Inorganic ion transport and metabolism].	3.74956e-65
NZ_CP019636.1\|WP_087541917.1\|4937615_4937924_-\|metal-sensitive-transcriptional-regulator	gnl\|CDD\|197393	cd10158, CsoR-like_DUF156_1, Uncharacterized family 1; belongs to a superfamily containing the transcriptional regulators CsoR (copper-sensitive operon repressor), RcnR, and FrmR, and related domains; this family was previously known as part of DUF156. Uncharacterized family 1, belonging to a larger superfamily that contains various transcriptional regulators that respond to different stressors such as Cu(I), Ni(I), sulfite, and formaldehyde, and includes CsoRs (copper-sensitive operon repressors). CsoRs form homotetramers (dimer of dimers). In Mycobacterium tuberculosis CsoR, within each dimer, two Cys residues on opposite subunits, along with a His residue, bind the Cu(I) ion (forming a triagonal S2N coordination complex, C-H-C). These residues are conserved in the majority of members of this superfamily, including this family; however, a conserved Tyr and a Glu residue that facilitates allosteric regulation of DNA binding for CsoRs are poorly conserved.	1.74336e-28
NZ_CP019636.1\|WP_087541906.1\|4922114_4923371_-\|CRISPR-associated-RAMP-protein-Csx10	gnl\|CDD\|131722	TIGR02674, cas_cyan_RAMP_2, CRISPR-associated RAMP protein, Csx10 family. CRISPR is a widespread repeat family in prokaryotes. At least 45 different protein families occur in prokaryotes only when these repeats are present. This family, a minor CRISPR-associated protein family, seems largely restricted to the Cyanobacteria. It belongs to the RAMP superfamily (pfam03787).	1.59599e-132
NZ_CP019636.1\|WP_087546273.1\|4928518_4929445_-\|CRISPR-associated-protein-Csx3	gnl\|CDD\|370583	pfam09620, Cas_csx3, CRISPR-associated protein (Cas_csx3). This entry is encoded in CRISPR-associated (cas) gene clusters, near CRISPR repeats, in the genomes of several different thermophiles: Archaeoglobus fulgidus (archaeal), Aquifex aeolicus (Aquificae), Dictyoglomus thermophilum (Dictyoglomi), and a thermophilic Synechococcus (Cyanobacteria). It is not yet assigned to a specific CRISPR/cas subtype (hence the x designation csx3).	5.46021e-33
NZ_CP019636.1\|WP_087541908.1\|4924071_4926414_-\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	gnl\|CDD\|274208	TIGR02577, thermophile-specific_DNA_repair_system, CRISPR-associated protein Cas10/Cmr2, subtype III-B. This model represent a Crm2 family of the CRISPR-associated RAMP module, a set of six genes recurring found together in prokaryotic genomes. This gene cluster is found only in species with CRISPR repeats, usually near the repeats themselves. Because most of the six (but not this family) contain RAMP domains, and because its appearance in a genome appears to depend on other CRISPR-associated Cas genes, the set is designated the CRISPR RAMP module. This protein, typified by TM1794 from Thermotoga maritima, is designated Crm2, for CRISPR RAMP Module protein 2.	2.21128e-42
NZ_CP019636.1\|WP_087541907.1\|4923367_4924075_-\|CRISPR-associated-protein-Csm3	gnl\|CDD\|224256	COG1337, COG1337, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.25632e-35
NZ_CP019636.1\|WP_087538405.1\|4940102_4941074_-\|AAA-family-ATPase	gnl\|CDD\|225806	COG3267, ExeA, Type II secretory pathway, component ExeA (predicted ATPase) [Intracellular trafficking and secretion].	3.78807e-53
NZ_CP019636.1\|WP_087546274.1\|4930661_4932029_+\|TIGR03985-family-CRISPR-associated-protein	gnl\|CDD\|274901	TIGR03985, hypothetical_protein_sll7078, CRISPR-associated protein, TIGR03985 family. Members of this protein family belong to CRISPR-associated (Cas) gene clusters. The majority of members are Cyanobacterial.	1.09463e-131
NZ_CP019636.1\|WP_087541911.1\|4927596_4928451_-\|hypothetical-protein	gnl\|CDD\|187833	cd09702, Csx1_III-U, CRISPR/Cas system-associated protein Csx1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Protein of this family often fused to HTH domain; Some proteins could have an additional fusion with RecB-family nuclease domain; Core domain appears to have a Rossmann-like fold; loosely associated with CRISPR/Cas systems; also known as TIGR02710 family.	0.0045247
NZ_CP019636.1\|WP_087541918.1\|4938263_4939331_+\|zinc-ABC-transporter-substrate-binding-protein	gnl\|CDD\|376518	pfam01297, ZnuA, Zinc-uptake complex component A periplasmic. ZnuA includes periplasmic solute binding proteins such as TroA that interacts with an ATP-binding cassette transport system in Treponema pallidum. ZnuA is part of the bacterial zinc-uptake complex ZnuABC, whose components are the following families, ZinT, pfam09223, pfam00950, pfam00005, all of which are regulated by the transcription-regulator family FUR, pfam01475. ZinT acts as a Zn2+-buffering protein that delivers Zn2+ to ZnuA (TroA), a high-affinity zinc-uptake protein. In Gram-negative bacteria the ZnuABC transporter system ensures an adequate import of zinc in Zn2+-poor environments, such as those encountered by pathogens within the infected host.	4.48836e-85

>NZ_CP019636.1|WP_087546274.1|4930661_4932029_+|TIGR03985-family-CRISPR-associated-protein
MRLWVLLNKLYSEEHWASSLPKIFTYAQLRDRLFSPTHSRSDKLSASQVVNSCQDLSCICHKSLQDWVFHTDTYLSKSEWQQAVVQLTGISTTDLEQQLQQYPFATVHRSIREDLKYLTQQGWLVAHSQGQYSCRPFQELPTPPTAISPAPNFAQLSVPQTWELLRVLESISFVQPNLEVVVRDLWEQVTDIATPSHKLKTEPQQRIFIHLDYILSDEMQDRVDTHQEQIEQLWHRPPGGVVQFEYWLASEERKVNVTVYPVCLHYLRRAKYLSAYGIDPQGKIDWHNYRLDRIASPHLQVLAWGDPSVPKPLKELWRTGQLPQPEEVKQHLDTAWGFNFYLKRELLILRFPPAFARWYVDDTVRHPTFQPVDYEQLPKLIATSVLSPVEQKQLLEIIKQRDKNDRYYQAWIRTGDINVLMRLRDWRPNGEVIAPLSVRHRLKEEAIQELSNYQI
>NZ_CP019636.1|WP_157679566.1|4930221_4930413_+|hypothetical-protein
MWSSVLSEPVVDYLFPARGRKLQQHHGIQILRLCRGRRLPFPRKGTETHERARQVLRTVFQEL
>NZ_CP019636.1|WP_087546273.1|4928518_4929445_-|CRISPR-associated-protein-Csx3
MNPSHPSIRLHLSHHENPQGLKYQQLTIELTRKDRIIYPEEIADLELPSGIDTTCGVVISGRAPIWLHGYLMYELHPTAWVAYYEPRMYSAIVAATQTRQVKIGQVIPLEQKGDGTLCAGLMIVGPPDSGKSVLSHTLFKALLADHPDIYLQRANWDGEGNYVLESVFTEEQQEAFKAANKGGLTERFFPYHAQAILQLRRQKALVIVDVGGMVQPEKQPILEACSHYIIISSKPEAIPAWHEFCRDSGNLKPVAVIHSTLSECEIIHQQEPYVEITCGPWVRGQATEVPVSLLECVRPIVKHLVAEG
>NZ_CP019636.1|WP_087541911.1|4927596_4928451_-|hypothetical-protein
MLGPKHKRYVKLENIFSPRSPLEFLGFSLVGVIINLLSGAHPAGFIGVVVLFLCWWILDVWRSKNLSKQLGFSITKKSPKAAKGLILLLSPYSPQSMALKDEQKLKPLITKILTMPHDTLSEADFNDIDLFNSNLLPQIKAVEYHWEQSTLDDVWLISSESYENVRGSEETAQILEKYLRFHYGKVLNIHSQGLVVKDWDYKTLWQLGEDIFRRSDYKEQAIVVDITGGTKMMSVALAMVCIPPNRQMQYMDSQRDWQGNPLPKGEMKPVVIDINPFLYPFLED
>NZ_CP019636.1|WP_087541910.1|4927151_4927574_+|hypothetical-protein
MIKTTSDTQTPEIKRNYISQLLEQLTVDYQNTKQERKEITALYPAGDEEFSILEEIELLTVDIRGYASQIQARGSIENEQQAIERLQKMRVFDIPVITEFYFTSNRSYRQMKAYLQMLDYLRLLIIEYLQIYQISQPQSA
>NZ_CP019636.1|WP_087541909.1|4926814_4927159_+|hypothetical-protein
MYDEPPADPFFAQLCEGYTEAEVAEIQQYMAEWDASTYISVAQTIVDHASRKEFDPLKYLRKAHNFNKKRAARIPKSGYRQDGSAVYRKGNEYLIVRPDKLGIEKIVTYGLNDD
>NZ_CP019636.1|WP_087541908.1|4924071_4926414_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MTNSQHSITTAISWCLAWGDKREPNFDIAVLQQMRQALNDGKDVPEKVRSLVEQVKQLQGIDKDYFPETLDELKSKYPELCNQTTRIGLVYGGATKIKQYVFESSKIQDIRGASALLDRINLIDLPAFFNKNPQSSNSYTIQCNQVRQWLDQKFSAGYKLSQILIPELIIYSTGGNILAFCPAAFVDDLANAIEKRYTEETLTANSCAVGEKFRLLELRFGLLREPIENMQWLDWYYREYDKPLVQAYFGYPTNDSEKLEAFKNRKSFNELTTKLAILFNQRRSGHDFSNRPSRRYPPMFETHPYLMRDEGERRSAVMIVQPPELPKKSHFSEASARKHLVGYRAKKGKPDLPEWYKNSHLTWESIRVEGWVDKFNSFLNKNPNLKQKYYANLKHDNIEIPQNLSHIANASKDFIAYIYADGNNMGGYIQKIRTSQKYQEFSQDVELATEYAVYQALAENLHPHELRNFKDEESTLSNGDLVHPFEIITIGGDDIILIVPANKALQIAQMIGERFEKILLKQVPLVENSTAEEKINGCYRIKTSDKPTDLKKCHRYKPTEATPSQCELSTSIGVLITAYNTPIYYAKGLTEQLLKSAKDRGKKLKEAGYCGGTVDFLTMKSVTMISSDIKEFRQQALTKNLKSKLKLYAAPYTLHELGGLITAIKALKKAHFPKSQLYQIRSLLERGKHTAILNYRYFRVRLKQGKAELQTDFENAWCQPKDENNGGNLAPWMYDDGKIDPKNLEDPFYETIWREMVELYEFIEIPDSELSELSSVGTEL
>NZ_CP019636.1|WP_087541907.1|4923367_4924075_-|CRISPR-associated-protein-Csm3
MINLQELSNPITSYQITAVIDTALCVGAGGSSGSLADKPIVRNSEGNLLIPASQLKGRLRHECEKIARGLCWHICYSPNPQTMCPQRAGLTGNFERTEYHVSGYEGHHHCLICQIFGNPVLPSRVIFDDLICTEDPDNLPEVLRPGVTINRRRCTAEEQKLYFLETSPTNAQLRFTGHIHLSRVPVYAGALILAGLRHINALGGSKSAGLGWLHWQFPNLPVEQAAWNFLARGVQ
>NZ_CP019636.1|WP_087541906.1|4922114_4923371_-|CRISPR-associated-RAMP-protein-Csx10
MKRIDLEIKALSPLAIGRQKPGGSISEAESYIPGSVIRGAIAAHILNQANTSITDGDNFYELFLGESPAIFQNAYPATIEEGKQTRGQSEVKVLPATALSSKIKSGFKSKPNDPKHNGVFDTLIDRFCAEGYGQLYDPNCPTERRVDGDRVDNFTGFYSQLKEKYYGHSVTSRLLTRTGINRRRATSEERVLYSIEVLNESQDNRQISIIYTGAILVADELAESLQEFIKNHKEDLRLGGATSRGLGRVKITPKPPVELKPKVTDKIKQFNDKLRQRWCQWKNIFGNPIKDLLENRDYFTLDLQADAILIDNWRRTTVISSEMLQQFTAVSDSSLQLHAAYSSYDYRSGWNSAWGLMKDMELITNKGSVYLFSTAEKDLWSKALEDLEVKGVGDHTCEGFGQVQICNPFHLVMREEAV
>NZ_CP019636.1|WP_087541905.1|4921707_4922118_-|hypothetical-protein
MSLPIESKTELKVQKGIRQVEDDLVIWIQEALDNANYGDLEESQFRNLVRVSDTTESVEAIKNFIRYQVGRDRKWGRGEDSLAQNIIEDIDNNIRESAQTIAEYCQTDFKPIWLELIRRYLGYGARYLKYLRDGNV
>NZ_CP019636.1|WP_087541913.1|4933653_4934070_-|hypothetical-protein
MEVYLNTQVDLNSAIDQVWRSLSERNQQWKQRQEAAIAQAKQILAQQFQQDLTEVLPSEIQNSLGIQIKQSLDISDISADFEFMDSPFSIKRIWLSDSMYWRIVHLKENIDCQPENLKNQLLRELAKLKNQSNTESQS
>NZ_CP019636.1|WP_087541914.1|4934078_4936319_-|hypothetical-protein
MPSYTRNVKRDNLVFVPVNPKILYGFKTKDLTSISGVSAADIAPLGHLTATAASGRAGAILVVGANAPKPPRVTKRISAAAAGVQQSVSTFCATSSLAGALAAGWNVAKPGRGVLTRNASASRGTLTAIATLSNGARYCFPMNKADFDAHGAALGLESAATITNQGERDSLVRGTRLPRPGRASLEVAGGGTFVSFFSSSFSGELGKNNFHQLSEEVILNGAAPAAADIVRESLSSELTRSQIGRAGVRVFRALQTTQTDSNGNIIRWLWNAGNQFFGLIGAAFKIIGVSFTALWALVVSTVQYVWNFNWNISDRELDQQLQNSLNVLAALLGGTVGNSIGYLACGVLPGAYIFSLNEPLGAHVLANVAEEMAEEFLANVNNLIRYSFISGVQALLMWGFRNVRKLIKSNIAFVQAVFGDKAARAVQAWGQPNSKPWSFALALNNAVESIPNTAVQNFVEEFLEEAWEGCVEAGYVVANSLDAYIAQQKLASQQQLILGQQRYVEVQPDRTNERERIILAGPEQPLKAALVQTLSNYQLIENRDVGQLVGMPADDYLRAKPQSIRLVITFSSVSSPPWKAAAGQRLVTATYAVPDVKRSKCDWETIKQACGGRNGYLWGRYRATGILSNGRQMQVMGATGDEAEDRLRALVALSEATLVKKPTISEDRSEDASGSYTKQPTRIYPAFCTIMNQYQVPGARGSSIRLNGGEYMRRQDKILLWTEEKPFGTDELIAELLRKPGAEEHT
>NZ_CP019636.1|WP_087541915.1|4936585_4936828_+|hypothetical-protein
MELKAFPLLDTRCKRLMLRRKHRVGKRGRQTYHYRPQQRLINRLAAQLQMPPQAVRQQIAQERLYLLRQMYGPDIGPQDV
>NZ_CP019636.1|WP_087541916.1|4936947_4937130_+|hypothetical-protein
MSLQELKEQIYKLSVSDHLTLVSAIIQSLQDAPQAEDWQYLVTRPHSWRKQLYIKVELTH
>NZ_CP019636.1|WP_087541917.1|4937615_4937924_-|metal-sensitive-transcriptional-regulator
MDSEEKTLPNLQHSYSEASLQDLMKRLSRIEGHIRGVKNMVESSRPCPDVLIQIAAVRGAVQQVGRIILNEYLKESVARTTKEGDIKTEIAALKTVLDRFLT
>NZ_CP019636.1|WP_087541918.1|4938263_4939331_+|zinc-ABC-transporter-substrate-binding-protein
MKTSALLLVFSLTLTACNAPQNTAVSPTPSQSTATVQPVQNQTKSKTLVVTTVAPLTNIVSNIAGERLEVKGIIPEGTDSHTFEPRPSDTDLLSKANLIIVNGLHLESPTEKLAKASKPQQTNIYELGSNTITESQWIYDFSFPKEKGDPNPHLWVNPKYAEAYAKLAAKQLTQLDPEGKDYYAKNLNNYLQRLDALDKVTREVVASIPAKNRKLLTYHDSWAYWAREYGFQVIGAIQPSDFKEPSAQDVAKLIEQIRKLGVPAIFGSEVYPSKVEEQIAREAKVKTANTADDELPGTGSANAIENTNPQHTYIGMMANNLRIIAENLGGNPKLVDKLNTTNVVGPTATTATTTQ
>NZ_CP019636.1|WP_087538405.1|4940102_4941074_-|AAA-family-ATPase
MLTEVMEFYGLVKEFRRAGYYETDHLRQLFKEIKAAIPQGKMIAVTGVVGCGKTVTLRRLQEALKKEGKILVSKSLSVDKNRATLPTLIAALFYDLSSDKEVKISTQGEKRERELQELIRKGKKPVALFVDEAHDLHSSTLTGLKRLIEVVEDSGGILSIILAGHPKLKNDLRRPMMEEIGYRTVIFSLDSIGGSQRQYIEWLLSSCTKEGTLLENLITAEAIDLLCTRLRTPLQIEMHLSLSFEEAHRMGEAIVTLSIVESILSKQIDDLEPTLTRHGYNVKSLSEQLNAKPSEIRSLLRGQLDPTRTRELQEQMLAAGLPI
>NZ_CP019636.1|WP_087538406.1|4942718_4943282_-|recombinase-family-protein
MLIGYARVSTDDQNLNLQKDALKQAGCSRIYEDRLSGAGVARPGLTKALEAARAGDVLVVWRLDRLGRSLKDLIQMVETLSERGIELHSLTEALATTSTSGKLIFHLFGALAEFERNLIRERTQAGLTAARARGRKGGRPKALDAPKRQLAIKLYNERQYTIEEICRIMGISKPTLYSYIAKAQGTP
>NZ_CP019636.1|WP_087541919.1|4943936_4944797_+|metal-ABC-transporter-permease
MEFLLKPFQYEFFSRAVAVGMMAGLLCGVMGVYIITRRMSYIAHGLSHAILGGAVLSYVLGLNFYIGSGIWGFAAALLIQYLTGRKVYSDAAIGIVTTASFALGVAVISTYRKFSQNFEAALFGNVLGVSPSDLWFVTAVTIVILSLCFFFYRPLLFWCFDREVAQVHGVPVVAMDTLFALMLATLLVATLNVLGVTLIISAVVIPASIARLLSDRFGSVIVISGVLGAAIAFIGIYLSYYLDIASGASVVLLSTLVFGCVLLWKSIQSRRKRYVPPLSSQHYQDY
>NZ_CP019636.1|WP_087541920.1|4946941_4949737_+|hypothetical-protein
MLHKLICGWQNINLSLLTILLTSIFMFDRVDAKNQAYTNVSVLASTSELEINTDSHSRKSLLSRQPQIFKKYYIVQKLNQEPIKFFPDINIPELPKNTLPESNTNHLNPNNSNRQNQTPDLNNKNLELLILDSLTNSSNKYPWIVYPTDEFRFSSVFNPTKNTNYIDFSFDLKSHEPIFEYLVFASFPKQKQFYWSLPGNRIVMETQGWQGGIFDQGQSTKIESRQLIMLTQKLWGMQAVSVIPQSFKDLTGEIDTNNFSIQSIAAEAIIPPGFPTPKIIIDNGNSNSTIKNIPRISNLGTASTYSPKGGESLFGFLDANNAPLLLQTFPTSNLQPLLEAGNLSRGTIISQDTLAKIGFYWGNPFTGEATRFQPPMTSKPGLKIGQIGQFDNWSLLNILINPFLSAKERNLYYLNSLYWVPLGQRISNITLNQRQENYHWQRFYLSRPHNRTLLEYDPVKAQGTYTNIFSNPGISLSLLANQGEIDELQSANTTLGMLMGGIFEFIHLPELEQSLQEAKKRFAQKENLTDLNLKATPDQIRQINQLLNRTLLLGNRNSRLEQVSGTLTFPSKITPNSSNILQIRTGNYQRAVQFADGNLTWIKGQTFISRADISNTSFGPLTFIGIPVPLEQTSILPSNRTAVAQVTLTDSNGQQFVQNWSLADTTEVPMNIRSFAIAFDHIELSQANQLITKSQTFNGHLFLPTLEVLWAGSSGNWNYSINSGIWFNLNSNSAFNVANNSLGLSEPTVGVYANGALSYIKTHVEVDTKGQIQAIISHIPSFRFYWNSAANSQNPTYLNFSYSFSRQDHNLNYSLAPAIIFFYNQGQLTPAGFLQGKLLLNQGLELSNFLQIGDHFLYKFTGIQKLNQNWSVGAYLQNFTEINQVIRTNNNDLSYGLITKHTSANGNNFWESQIGMNGDNFEVRFQRGWRF

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Crispr_ID: NZ_CP019636_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_14

4930025-4930515

TypeIII

Consensus_repeat	Method
GTCGTAGACTACCTTTTCCCCGCAAGGGGACGGAAAC	PILER-CR
ACTACCTTTTCCCCGCAAGGGGACGGAAAC	CRT
TTTCCCCGCAAGGGGACGGAAAC	CRISPRCasFinder

6 spacers

csx3,cas10,csm3gr7,csx10gr5,csm2gr11,csx1,WYL

The CRISPR arrays of NZ_CP019636_14

>merge|NZ_CP019636|14|4930025-4930515|PILER-CR,CRT,CRISPRCasFinder
GTCGTAGACTACCATTTCCCCGCAAGGGGACGGAAACTGGCGCTGGATTTGGACAGTGTCCTGTTGATCTTGGACAGTCGTAGACTACCTTTCCCCGCAAGGGGACGGAAACCTTTGTTGAGCGTATTGTCTTCTTGCGTGGAGTTTCGAGAGTCGTAGACTACCTTTTCCCCACAAGGGGACGGAAACGTCGGGTAATGTGGTCCAGTGTGTTGTCTGAACCAGTCGTAGACTACCTTTTCCCCGCAAGGGGACGGAAACTCCAGCAGCATCACGGCATTCAGATACTAAGGCTGTGTCGTGGTCGTAGACTACCTTTTCCCCGCAAGGGGACGGAAACGCATGAACGTGCACGCCAGGTTCTTCGTACGGTTTTTCAAGAGTTGTAAACTACCTGTTCCCCGCAAGGGGACGGAAACTAGCCTGGGATAGTATATTCGATATGATCCCCGAAGTCGTAGACTACCTTTTCCCCGTAAGGGGAAGGAAAC

>NZ_CP019636|14|5|4930025-4930515|PILER-CR
GTCGTAGACTACCATTTCCCCGCAAGGGGACGGAAAC	TGGCGCTGGATTTGGACAGTGTCCTGTTGATCTTGGACA
GTCGTAGACTACCTTTCCCCGCAAGGGGACGGAAACC	TTTGTTGAGCGTATTGTCTTCTTGCGTGGAGTTTCGAGAG
TCGTAGACTACCTTTTCCCCACAAGGGGACGGAAACG	TCGGGTAATGTGGTCCAGTGTGTTGTCTGAACCAG
TCGTAGACTACCTTTTCCCCGCAAGGGGACGGAAACT	CCAGCAGCATCACGGCATTCAGATACTAAGGCTGTGTCGTGG
TCGTAGACTACCTTTTCCCCGCAAGGGGACGGAAACG	CATGAACGTGCACGCCAGGTTCTTCGTACGGTTTTTCAAGAG
TTGTAAACTACCTGTTCCCCGCAAGGGGACGGAAACT	AGCCTGGGATAGTATATTCGATATGATCCCCGAAG
TCGTAGACTACCTTTTCCCCGTAAGGGGAAGGAAAC

>NZ_CP019636|14|5|4930032-4930515|CRT
ACTACCATTTCCCCGCAAGGGGACGGAAAC	TGGCGCTGGATTTGGACAGTGTCCTGTTGATCTTGGACAGTCGTA
GACTACCTTTCCCCGCAAGGGGACGGAAAC	CTTTGTTGAGCGTATTGTCTTCTTGCGTGGAGTTTCGAGAGTCGTAG
ACTACCTTTTCCCCACAAGGGGACGGAAAC	GTCGGGTAATGTGGTCCAGTGTGTTGTCTGAACCAGTCGTAG
ACTACCTTTTCCCCGCAAGGGGACGGAAAC	TCCAGCAGCATCACGGCATTCAGATACTAAGGCTGTGTCGTGGTCGTAG
ACTACCTTTTCCCCGCAAGGGGACGGAAAC	GCATGAACGTGCACGCCAGGTTCTTCGTACGGTTTTTCAAGAGTTGTAA
ACTACCTGTTCCCCGCAAGGGGACGGAAAC	TAGCCTGGGATAGTATATTCGATATGATCCCCGAAGTCGTAG
ACTACCTTTTCCCCGTAAGGGGAAGGAAAC

>NZ_CP019636|14|14|4930039-4930515|CRISPRCasFinder
TTTCCCCGCAAGGGGACGGAAAC	TGGCGCTGGATTTGGACAGTGTCCTGTTGATCTTGGACAGTCGTAGACTACC
TTTCCCCGCAAGGGGACGGAAAC	CTTTGTTGAGCGTATTGTCTTCTTGCGTGGAGTTTCGAGAGTCGTAGACTACCT
TTTCCCCACAAGGGGACGGAAAC	GTCGGGTAATGTGGTCCAGTGTGTTGTCTGAACCAGTCGTAGACTACCT
TTTCCCCGCAAGGGGACGGAAAC	TCCAGCAGCATCACGGCATTCAGATACTAAGGCTGTGTCGTGGTCGTAGACTACCT
TTTCCCCGCAAGGGGACGGAAAC	GCATGAACGTGCACGCCAGGTTCTTCGTACGGTTTTTCAAGAGTTGTAAACTACCT
GTTCCCCGCAAGGGGACGGAAAC	TAGCCTGGGATAGTATATTCGATATGATCCCCGAAGTCGTAGACTACCT
TTTCCCCGTAAGGGGAAGGAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087541914.1\|4934078_4936319_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541905.1\|4921707_4922118_-\|hypothetical-protein	csm2gr11	mkCas0063_csm2gr11_CAS-III-D	unknown
NZ_CP019636.1\|WP_087541918.1\|4938263_4939331_+\|zinc-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|376518
NZ_CP019636.1\|WP_087546274.1\|4930661_4932029_+\|TIGR03985-family-CRISPR-associated-protein	WYL	mkCas0075_WYL_CAS-I:CAS-III	gnl\|CDD\|274901
NZ_CP019636.1\|WP_087546273.1\|4928518_4929445_-\|CRISPR-associated-protein-Csx3	csx3	mkCas0115_csx3_CAS-I:CAS-III	gnl\|CDD\|370583
NZ_CP019636.1\|WP_087541908.1\|4924071_4926414_-\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl\|CDD\|274208
NZ_CP019636.1\|WP_087541907.1\|4923367_4924075_-\|CRISPR-associated-protein-Csm3	csm3gr7	COG1337_csm3gr7_CAS-III-D	gnl\|CDD\|224256
NZ_CP019636.1\|WP_087541919.1\|4943936_4944797_+\|metal-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224033
NZ_CP019636.1\|WP_087541909.1\|4926814_4927159_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541906.1\|4922114_4923371_-\|CRISPR-associated-RAMP-protein-Csx10	csx10gr5	cd09700_csx10gr5_CAS-III-D	gnl\|CDD\|131722
NZ_CP019636.1\|WP_087541911.1\|4927596_4928451_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|187833
NZ_CP019636.1\|WP_087541917.1\|4937615_4937924_-\|metal-sensitive-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197393
NZ_CP019636.1\|WP_087541910.1\|4927151_4927574_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538406.1\|4942718_4943282_-\|recombinase-family-protein	unknown	unknown	gnl\|CDD\|239737
NZ_CP019636.1\|WP_087541915.1\|4936585_4936828_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538405.1\|4940102_4941074_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|225806
NZ_CP019636.1\|WP_087546013.1\|4918963_4920343_+\|IS110-family-transposase	unknown	unknown	gnl\|CDD\|376564
NZ_CP019636.1\|WP_087541904.1\|4920480_4921644_-\|DUF1887-family-protein	csx1	pfam09002_csx1_CAS-III	gnl\|CDD\|312526
NZ_CP019636.1\|WP_087541916.1\|4936947_4937130_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541913.1\|4933653_4934070_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087541918.1\|4938263_4939331_+\|zinc-ABC-transporter-substrate-binding-protein	gnl\|CDD\|376518	pfam01297, ZnuA, Zinc-uptake complex component A periplasmic. ZnuA includes periplasmic solute binding proteins such as TroA that interacts with an ATP-binding cassette transport system in Treponema pallidum. ZnuA is part of the bacterial zinc-uptake complex ZnuABC, whose components are the following families, ZinT, pfam09223, pfam00950, pfam00005, all of which are regulated by the transcription-regulator family FUR, pfam01475. ZinT acts as a Zn2+-buffering protein that delivers Zn2+ to ZnuA (TroA), a high-affinity zinc-uptake protein. In Gram-negative bacteria the ZnuABC transporter system ensures an adequate import of zinc in Zn2+-poor environments, such as those encountered by pathogens within the infected host.	4.48836e-85
NZ_CP019636.1\|WP_087541906.1\|4922114_4923371_-\|CRISPR-associated-RAMP-protein-Csx10	gnl\|CDD\|131722	TIGR02674, cas_cyan_RAMP_2, CRISPR-associated RAMP protein, Csx10 family. CRISPR is a widespread repeat family in prokaryotes. At least 45 different protein families occur in prokaryotes only when these repeats are present. This family, a minor CRISPR-associated protein family, seems largely restricted to the Cyanobacteria. It belongs to the RAMP superfamily (pfam03787).	1.59599e-132
NZ_CP019636.1\|WP_087546273.1\|4928518_4929445_-\|CRISPR-associated-protein-Csx3	gnl\|CDD\|370583	pfam09620, Cas_csx3, CRISPR-associated protein (Cas_csx3). This entry is encoded in CRISPR-associated (cas) gene clusters, near CRISPR repeats, in the genomes of several different thermophiles: Archaeoglobus fulgidus (archaeal), Aquifex aeolicus (Aquificae), Dictyoglomus thermophilum (Dictyoglomi), and a thermophilic Synechococcus (Cyanobacteria). It is not yet assigned to a specific CRISPR/cas subtype (hence the x designation csx3).	5.46021e-33
NZ_CP019636.1\|WP_087541908.1\|4924071_4926414_-\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	gnl\|CDD\|274208	TIGR02577, thermophile-specific_DNA_repair_system, CRISPR-associated protein Cas10/Cmr2, subtype III-B. This model represent a Crm2 family of the CRISPR-associated RAMP module, a set of six genes recurring found together in prokaryotic genomes. This gene cluster is found only in species with CRISPR repeats, usually near the repeats themselves. Because most of the six (but not this family) contain RAMP domains, and because its appearance in a genome appears to depend on other CRISPR-associated Cas genes, the set is designated the CRISPR RAMP module. This protein, typified by TM1794 from Thermotoga maritima, is designated Crm2, for CRISPR RAMP Module protein 2.	2.21128e-42
NZ_CP019636.1\|WP_087541907.1\|4923367_4924075_-\|CRISPR-associated-protein-Csm3	gnl\|CDD\|224256	COG1337, COG1337, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.25632e-35
NZ_CP019636.1\|WP_087546274.1\|4930661_4932029_+\|TIGR03985-family-CRISPR-associated-protein	gnl\|CDD\|274901	TIGR03985, hypothetical_protein_sll7078, CRISPR-associated protein, TIGR03985 family. Members of this protein family belong to CRISPR-associated (Cas) gene clusters. The majority of members are Cyanobacterial.	1.09463e-131
NZ_CP019636.1\|WP_087541911.1\|4927596_4928451_-\|hypothetical-protein	gnl\|CDD\|187833	cd09702, Csx1_III-U, CRISPR/Cas system-associated protein Csx1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Protein of this family often fused to HTH domain; Some proteins could have an additional fusion with RecB-family nuclease domain; Core domain appears to have a Rossmann-like fold; loosely associated with CRISPR/Cas systems; also known as TIGR02710 family.	0.0045247
NZ_CP019636.1\|WP_087538406.1\|4942718_4943282_-\|recombinase-family-protein	gnl\|CDD\|239737	cd03768, SR_ResInv, Serine Recombinase (SR) family, Resolvase and Invertase subfamily, catalytic domain; members contain a C-terminal DNA binding domain. Serine recombinases catalyze site-specific recombination of DNA molecules by a concerted, four-strand cleavage and rejoining mechanism which involves a transient phosphoserine linkage between DNA and the enzyme. They are functionally versatile and include resolvases, invertases, integrases, and transposases. Resolvases and invertases affect resolution or inversion and comprise a major phylogenic group. Resolvases (e.g. Tn3, gamma-delta, and Tn5044) normally recombine two sites in direct repeat causing deletion of the DNA between the sites. Invertases (e.g. Gin and Hin) recombine sites in inverted repeat to invert the DNA between the sites. Cointegrate resolution with gamma-delta resolvase requires the formation of a synaptosome of three resolvase dimers bound to each of two res sites on the DNA. Also included in this subfamily are some putative integrases including a sequence from bacteriophage phi-FC1.	1.3966e-60
NZ_CP019636.1\|WP_087541919.1\|4943936_4944797_+\|metal-ABC-transporter-permease	gnl\|CDD\|224033	COG1108, ZnuB, ABC-type Mn2+/Zn2+ transport systems, permease components [Inorganic ion transport and metabolism].	3.74956e-65
NZ_CP019636.1\|WP_087541917.1\|4937615_4937924_-\|metal-sensitive-transcriptional-regulator	gnl\|CDD\|197393	cd10158, CsoR-like_DUF156_1, Uncharacterized family 1; belongs to a superfamily containing the transcriptional regulators CsoR (copper-sensitive operon repressor), RcnR, and FrmR, and related domains; this family was previously known as part of DUF156. Uncharacterized family 1, belonging to a larger superfamily that contains various transcriptional regulators that respond to different stressors such as Cu(I), Ni(I), sulfite, and formaldehyde, and includes CsoRs (copper-sensitive operon repressors). CsoRs form homotetramers (dimer of dimers). In Mycobacterium tuberculosis CsoR, within each dimer, two Cys residues on opposite subunits, along with a His residue, bind the Cu(I) ion (forming a triagonal S2N coordination complex, C-H-C). These residues are conserved in the majority of members of this superfamily, including this family; however, a conserved Tyr and a Glu residue that facilitates allosteric regulation of DNA binding for CsoRs are poorly conserved.	1.74336e-28
NZ_CP019636.1\|WP_087538405.1\|4940102_4941074_-\|AAA-family-ATPase	gnl\|CDD\|225806	COG3267, ExeA, Type II secretory pathway, component ExeA (predicted ATPase) [Intracellular trafficking and secretion].	3.78807e-53
NZ_CP019636.1\|WP_087546013.1\|4918963_4920343_+\|IS110-family-transposase	gnl\|CDD\|376564	pfam01548, DEDD_Tnp_IS110, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family includes an amino-terminal region of the pilin gene inverting protein (PIVML) and of members of the IS111A/IS1328/IS1533 family of transposases. The C-terminus is represented by family pfam02371.	7.7599e-20
NZ_CP019636.1\|WP_087541904.1\|4920480_4921644_-\|DUF1887-family-protein	gnl\|CDD\|312526	pfam09002, DUF1887, Domain of unknown function (DUF1887). This domain is found in a set of hypothetical bacterial proteins.	2.52316e-11

>NZ_CP019636.1|WP_087546273.1|4928518_4929445_-|CRISPR-associated-protein-Csx3
MNPSHPSIRLHLSHHENPQGLKYQQLTIELTRKDRIIYPEEIADLELPSGIDTTCGVVISGRAPIWLHGYLMYELHPTAWVAYYEPRMYSAIVAATQTRQVKIGQVIPLEQKGDGTLCAGLMIVGPPDSGKSVLSHTLFKALLADHPDIYLQRANWDGEGNYVLESVFTEEQQEAFKAANKGGLTERFFPYHAQAILQLRRQKALVIVDVGGMVQPEKQPILEACSHYIIISSKPEAIPAWHEFCRDSGNLKPVAVIHSTLSECEIIHQQEPYVEITCGPWVRGQATEVPVSLLECVRPIVKHLVAEG
>NZ_CP019636.1|WP_087541911.1|4927596_4928451_-|hypothetical-protein
MLGPKHKRYVKLENIFSPRSPLEFLGFSLVGVIINLLSGAHPAGFIGVVVLFLCWWILDVWRSKNLSKQLGFSITKKSPKAAKGLILLLSPYSPQSMALKDEQKLKPLITKILTMPHDTLSEADFNDIDLFNSNLLPQIKAVEYHWEQSTLDDVWLISSESYENVRGSEETAQILEKYLRFHYGKVLNIHSQGLVVKDWDYKTLWQLGEDIFRRSDYKEQAIVVDITGGTKMMSVALAMVCIPPNRQMQYMDSQRDWQGNPLPKGEMKPVVIDINPFLYPFLED
>NZ_CP019636.1|WP_087541910.1|4927151_4927574_+|hypothetical-protein
MIKTTSDTQTPEIKRNYISQLLEQLTVDYQNTKQERKEITALYPAGDEEFSILEEIELLTVDIRGYASQIQARGSIENEQQAIERLQKMRVFDIPVITEFYFTSNRSYRQMKAYLQMLDYLRLLIIEYLQIYQISQPQSA
>NZ_CP019636.1|WP_087541909.1|4926814_4927159_+|hypothetical-protein
MYDEPPADPFFAQLCEGYTEAEVAEIQQYMAEWDASTYISVAQTIVDHASRKEFDPLKYLRKAHNFNKKRAARIPKSGYRQDGSAVYRKGNEYLIVRPDKLGIEKIVTYGLNDD
>NZ_CP019636.1|WP_087541908.1|4924071_4926414_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MTNSQHSITTAISWCLAWGDKREPNFDIAVLQQMRQALNDGKDVPEKVRSLVEQVKQLQGIDKDYFPETLDELKSKYPELCNQTTRIGLVYGGATKIKQYVFESSKIQDIRGASALLDRINLIDLPAFFNKNPQSSNSYTIQCNQVRQWLDQKFSAGYKLSQILIPELIIYSTGGNILAFCPAAFVDDLANAIEKRYTEETLTANSCAVGEKFRLLELRFGLLREPIENMQWLDWYYREYDKPLVQAYFGYPTNDSEKLEAFKNRKSFNELTTKLAILFNQRRSGHDFSNRPSRRYPPMFETHPYLMRDEGERRSAVMIVQPPELPKKSHFSEASARKHLVGYRAKKGKPDLPEWYKNSHLTWESIRVEGWVDKFNSFLNKNPNLKQKYYANLKHDNIEIPQNLSHIANASKDFIAYIYADGNNMGGYIQKIRTSQKYQEFSQDVELATEYAVYQALAENLHPHELRNFKDEESTLSNGDLVHPFEIITIGGDDIILIVPANKALQIAQMIGERFEKILLKQVPLVENSTAEEKINGCYRIKTSDKPTDLKKCHRYKPTEATPSQCELSTSIGVLITAYNTPIYYAKGLTEQLLKSAKDRGKKLKEAGYCGGTVDFLTMKSVTMISSDIKEFRQQALTKNLKSKLKLYAAPYTLHELGGLITAIKALKKAHFPKSQLYQIRSLLERGKHTAILNYRYFRVRLKQGKAELQTDFENAWCQPKDENNGGNLAPWMYDDGKIDPKNLEDPFYETIWREMVELYEFIEIPDSELSELSSVGTEL
>NZ_CP019636.1|WP_087541907.1|4923367_4924075_-|CRISPR-associated-protein-Csm3
MINLQELSNPITSYQITAVIDTALCVGAGGSSGSLADKPIVRNSEGNLLIPASQLKGRLRHECEKIARGLCWHICYSPNPQTMCPQRAGLTGNFERTEYHVSGYEGHHHCLICQIFGNPVLPSRVIFDDLICTEDPDNLPEVLRPGVTINRRRCTAEEQKLYFLETSPTNAQLRFTGHIHLSRVPVYAGALILAGLRHINALGGSKSAGLGWLHWQFPNLPVEQAAWNFLARGVQ
>NZ_CP019636.1|WP_087541906.1|4922114_4923371_-|CRISPR-associated-RAMP-protein-Csx10
MKRIDLEIKALSPLAIGRQKPGGSISEAESYIPGSVIRGAIAAHILNQANTSITDGDNFYELFLGESPAIFQNAYPATIEEGKQTRGQSEVKVLPATALSSKIKSGFKSKPNDPKHNGVFDTLIDRFCAEGYGQLYDPNCPTERRVDGDRVDNFTGFYSQLKEKYYGHSVTSRLLTRTGINRRRATSEERVLYSIEVLNESQDNRQISIIYTGAILVADELAESLQEFIKNHKEDLRLGGATSRGLGRVKITPKPPVELKPKVTDKIKQFNDKLRQRWCQWKNIFGNPIKDLLENRDYFTLDLQADAILIDNWRRTTVISSEMLQQFTAVSDSSLQLHAAYSSYDYRSGWNSAWGLMKDMELITNKGSVYLFSTAEKDLWSKALEDLEVKGVGDHTCEGFGQVQICNPFHLVMREEAV
>NZ_CP019636.1|WP_087541905.1|4921707_4922118_-|hypothetical-protein
MSLPIESKTELKVQKGIRQVEDDLVIWIQEALDNANYGDLEESQFRNLVRVSDTTESVEAIKNFIRYQVGRDRKWGRGEDSLAQNIIEDIDNNIRESAQTIAEYCQTDFKPIWLELIRRYLGYGARYLKYLRDGNV
>NZ_CP019636.1|WP_087541904.1|4920480_4921644_-|DUF1887-family-protein
MSDRVMLVLIGGRSAVPAIAGVLHFLDEIDRIKFLLCRGDQYLQFQKNIERVIKNERKNLLCDNETDVKSVDPSKFDEVYSSVKKLCEGVENLKYVNLTTVPQTMAISVYSYVQENYKDTLVFSVNTDQSQIIPLAFKKEAVSFKKQITVENYVAMCGFNIFRNKLTYESKIEIAKYIVEHLEISKKILSVIRSSAGNGDSIKAPRGFRINEKDFTDLGILASELEVFLNKLESYAIIHQLEISNQRISFKIEKKEDYAFLAGEWLEVFVYVSAKECEFDSVEMGVEIDNYRGEIDVFCLKNANAMICECKTGGKLSSDDLSVLGSKAEKLGGNYCVKLFITSEFKVGEDFINKAKNNRVVIVSGNELIRISEILAKEMQSPTHSRR
>NZ_CP019636.1|WP_087546013.1|4918963_4920343_+|IS110-family-transposase
MKKQEQPIAAEQRNLPVINPNAAGIDIGADRHWVSVPVDRDSENVHSFACFTAELYAMADWLKQCGIETVAMESTGVYWIPVFQVLESRGFEVKLVNAHYVKTVPGRKTDVLDCQWLQKLHSYGLLSGSFRPDDQICVLRSYIRQRDNLIKSACVHVQRMQKALTEMNLQLHRVISDITGTTGLSIIKAIVRGERNPLTLAALKDGRIKASCEEIAAALTGDYRDELIFILQQELQLYEFYQTQILAVDAQIEQCLASFADRVDVTKKPLTKPKRRGKKQPGNAPQFDLRTHLYRISGVDFTQIQGFGALTVLILLSELGLDPTRFPTVKHFTSWLGLCPGSRVTGGKVKSSQTRSVVSRAANAFRMAAQTLCRSNSALGAYYRRMQAKIGAPKAITAAAHKLARIFYRLWTSGDKFIDPGVDAYEQQYRERVVNNLKKKALTFGLELIPISDSTQCVS
>NZ_CP019636.1|WP_087546274.1|4930661_4932029_+|TIGR03985-family-CRISPR-associated-protein
MRLWVLLNKLYSEEHWASSLPKIFTYAQLRDRLFSPTHSRSDKLSASQVVNSCQDLSCICHKSLQDWVFHTDTYLSKSEWQQAVVQLTGISTTDLEQQLQQYPFATVHRSIREDLKYLTQQGWLVAHSQGQYSCRPFQELPTPPTAISPAPNFAQLSVPQTWELLRVLESISFVQPNLEVVVRDLWEQVTDIATPSHKLKTEPQQRIFIHLDYILSDEMQDRVDTHQEQIEQLWHRPPGGVVQFEYWLASEERKVNVTVYPVCLHYLRRAKYLSAYGIDPQGKIDWHNYRLDRIASPHLQVLAWGDPSVPKPLKELWRTGQLPQPEEVKQHLDTAWGFNFYLKRELLILRFPPAFARWYVDDTVRHPTFQPVDYEQLPKLIATSVLSPVEQKQLLEIIKQRDKNDRYYQAWIRTGDINVLMRLRDWRPNGEVIAPLSVRHRLKEEAIQELSNYQI
>NZ_CP019636.1|WP_087541913.1|4933653_4934070_-|hypothetical-protein
MEVYLNTQVDLNSAIDQVWRSLSERNQQWKQRQEAAIAQAKQILAQQFQQDLTEVLPSEIQNSLGIQIKQSLDISDISADFEFMDSPFSIKRIWLSDSMYWRIVHLKENIDCQPENLKNQLLRELAKLKNQSNTESQS
>NZ_CP019636.1|WP_087541914.1|4934078_4936319_-|hypothetical-protein
MPSYTRNVKRDNLVFVPVNPKILYGFKTKDLTSISGVSAADIAPLGHLTATAASGRAGAILVVGANAPKPPRVTKRISAAAAGVQQSVSTFCATSSLAGALAAGWNVAKPGRGVLTRNASASRGTLTAIATLSNGARYCFPMNKADFDAHGAALGLESAATITNQGERDSLVRGTRLPRPGRASLEVAGGGTFVSFFSSSFSGELGKNNFHQLSEEVILNGAAPAAADIVRESLSSELTRSQIGRAGVRVFRALQTTQTDSNGNIIRWLWNAGNQFFGLIGAAFKIIGVSFTALWALVVSTVQYVWNFNWNISDRELDQQLQNSLNVLAALLGGTVGNSIGYLACGVLPGAYIFSLNEPLGAHVLANVAEEMAEEFLANVNNLIRYSFISGVQALLMWGFRNVRKLIKSNIAFVQAVFGDKAARAVQAWGQPNSKPWSFALALNNAVESIPNTAVQNFVEEFLEEAWEGCVEAGYVVANSLDAYIAQQKLASQQQLILGQQRYVEVQPDRTNERERIILAGPEQPLKAALVQTLSNYQLIENRDVGQLVGMPADDYLRAKPQSIRLVITFSSVSSPPWKAAAGQRLVTATYAVPDVKRSKCDWETIKQACGGRNGYLWGRYRATGILSNGRQMQVMGATGDEAEDRLRALVALSEATLVKKPTISEDRSEDASGSYTKQPTRIYPAFCTIMNQYQVPGARGSSIRLNGGEYMRRQDKILLWTEEKPFGTDELIAELLRKPGAEEHT
>NZ_CP019636.1|WP_087541915.1|4936585_4936828_+|hypothetical-protein
MELKAFPLLDTRCKRLMLRRKHRVGKRGRQTYHYRPQQRLINRLAAQLQMPPQAVRQQIAQERLYLLRQMYGPDIGPQDV
>NZ_CP019636.1|WP_087541916.1|4936947_4937130_+|hypothetical-protein
MSLQELKEQIYKLSVSDHLTLVSAIIQSLQDAPQAEDWQYLVTRPHSWRKQLYIKVELTH
>NZ_CP019636.1|WP_087541917.1|4937615_4937924_-|metal-sensitive-transcriptional-regulator
MDSEEKTLPNLQHSYSEASLQDLMKRLSRIEGHIRGVKNMVESSRPCPDVLIQIAAVRGAVQQVGRIILNEYLKESVARTTKEGDIKTEIAALKTVLDRFLT
>NZ_CP019636.1|WP_087541918.1|4938263_4939331_+|zinc-ABC-transporter-substrate-binding-protein
MKTSALLLVFSLTLTACNAPQNTAVSPTPSQSTATVQPVQNQTKSKTLVVTTVAPLTNIVSNIAGERLEVKGIIPEGTDSHTFEPRPSDTDLLSKANLIIVNGLHLESPTEKLAKASKPQQTNIYELGSNTITESQWIYDFSFPKEKGDPNPHLWVNPKYAEAYAKLAAKQLTQLDPEGKDYYAKNLNNYLQRLDALDKVTREVVASIPAKNRKLLTYHDSWAYWAREYGFQVIGAIQPSDFKEPSAQDVAKLIEQIRKLGVPAIFGSEVYPSKVEEQIAREAKVKTANTADDELPGTGSANAIENTNPQHTYIGMMANNLRIIAENLGGNPKLVDKLNTTNVVGPTATTATTTQ
>NZ_CP019636.1|WP_087538405.1|4940102_4941074_-|AAA-family-ATPase
MLTEVMEFYGLVKEFRRAGYYETDHLRQLFKEIKAAIPQGKMIAVTGVVGCGKTVTLRRLQEALKKEGKILVSKSLSVDKNRATLPTLIAALFYDLSSDKEVKISTQGEKRERELQELIRKGKKPVALFVDEAHDLHSSTLTGLKRLIEVVEDSGGILSIILAGHPKLKNDLRRPMMEEIGYRTVIFSLDSIGGSQRQYIEWLLSSCTKEGTLLENLITAEAIDLLCTRLRTPLQIEMHLSLSFEEAHRMGEAIVTLSIVESILSKQIDDLEPTLTRHGYNVKSLSEQLNAKPSEIRSLLRGQLDPTRTRELQEQMLAAGLPI
>NZ_CP019636.1|WP_087538406.1|4942718_4943282_-|recombinase-family-protein
MLIGYARVSTDDQNLNLQKDALKQAGCSRIYEDRLSGAGVARPGLTKALEAARAGDVLVVWRLDRLGRSLKDLIQMVETLSERGIELHSLTEALATTSTSGKLIFHLFGALAEFERNLIRERTQAGLTAARARGRKGGRPKALDAPKRQLAIKLYNERQYTIEEICRIMGISKPTLYSYIAKAQGTP
>NZ_CP019636.1|WP_087541919.1|4943936_4944797_+|metal-ABC-transporter-permease
MEFLLKPFQYEFFSRAVAVGMMAGLLCGVMGVYIITRRMSYIAHGLSHAILGGAVLSYVLGLNFYIGSGIWGFAAALLIQYLTGRKVYSDAAIGIVTTASFALGVAVISTYRKFSQNFEAALFGNVLGVSPSDLWFVTAVTIVILSLCFFFYRPLLFWCFDREVAQVHGVPVVAMDTLFALMLATLLVATLNVLGVTLIISAVVIPASIARLLSDRFGSVIVISGVLGAAIAFIGIYLSYYLDIASGASVVLLSTLVFGCVLLWKSIQSRRKRYVPPLSSQHYQDY

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Crispr_ID: NZ_CP019636_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_16

4932737-4933632

TypeIII

Consensus_repeat	Method
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	PILER-CR
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CRISPRCasFinder
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CRT

12 spacers

WYL,csx3,cas10,csm3gr7,csx10gr5,csm2gr11

The CRISPR arrays of NZ_CP019636_16

>merge|NZ_CP019636|16|4932737-4933632|PILER-CR,CRISPRCasFinder,CRT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTTAACAGGTGCATTCGCCGCGATAAACTTTTGAATCGGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACACAGAGGTAGAGCTCTGCTATCGAAAAGGTATAGTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACAATCATCCGCATTTTATGACACACAAAACATAAGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACATCTTATTTATAGGTCGAAAAACAAAAGCAGTTAGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACAGGAATTTGGTCGCAGAACCAGCCGCCGTGGAACCAGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCATATCTATTAGATCTACCATTCCCCTGGTCATAGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTAAAAGCTTCTTCATAGTTTGGGTCTAGTGGGTTGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCTCGAAACCGTGGGTCTTGTCTCAAGTGGTTGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCTTTGGAATCTGGAGTCCAGGAATGACCAGCTTGGGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTGTTTTGTCTCTAAACCAAGCGTAATCCCACCATAGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACTTGTGCATGGATGCAGCCATCTCAGCCTCAGCAGTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAACCGAAGAATTCCACGGCACCCTTTAGCGGGATTTCAGTGACAAACTCTGGAGCATACAGAATACGAGAACGGT

>NZ_CP019636|16|7|4932737-4933560|PILER-CR
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTAACAGGTGCATTCGCCGCGATAAACTTTTGAATCGG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ACAGAGGTAGAGCTCTGCTATCGAAAAGGTATAGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AATCATCCGCATTTTATGACACACAAAACATAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ATCTTATTTATAGGTCGAAAAACAAAAGCAGTTA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGGAATTTGGTCGCAGAACCAGCCGCCGTGGAACCAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CATATCTATTAGATCTACCATTCCCCTGGTCATA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TAAAAGCTTCTTCATAGTTTGGGTCTAGTGGGTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTCGAAACCGTGGGTCTTGTCTCAAGTGGTTG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTTGGAATCTGGAGTCCAGGAATGACCAGCTTGG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TGTTTTGTCTCTAAACCAAGCGTAATCCCACCATA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTGTGCATGGATGCAGCCATCTCAGCCTCAGCA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC

>NZ_CP019636|16|15|4932737-4933560|CRISPRCasFinder
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTAACAGGTGCATTCGCCGCGATAAACTTTTGAATCGG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ACAGAGGTAGAGCTCTGCTATCGAAAAGGTATAGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AATCATCCGCATTTTATGACACACAAAACATAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ATCTTATTTATAGGTCGAAAAACAAAAGCAGTTA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGGAATTTGGTCGCAGAACCAGCCGCCGTGGAACCAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CATATCTATTAGATCTACCATTCCCCTGGTCATA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TAAAAGCTTCTTCATAGTTTGGGTCTAGTGGGTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTCGAAACCGTGGGTCTTGTCTCAAGTGGTTG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTTGGAATCTGGAGTCCAGGAATGACCAGCTTGG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TGTTTTGTCTCTAAACCAAGCGTAATCCCACCATA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTGTGCATGGATGCAGCCATCTCAGCCTCAGCA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC

>NZ_CP019636|16|7|4932737-4933632|CRT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTAACAGGTGCATTCGCCGCGATAAACTTTTGAATCGG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ACAGAGGTAGAGCTCTGCTATCGAAAAGGTATAGT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AATCATCCGCATTTTATGACACACAAAACATAA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	ATCTTATTTATAGGTCGAAAAACAAAAGCAGTTA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	AGGAATTTGGTCGCAGAACCAGCCGCCGTGGAACCAG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CATATCTATTAGATCTACCATTCCCCTGGTCATA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TAAAAGCTTCTTCATAGTTTGGGTCTAGTGGGTT
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTCGAAACCGTGGGTCTTGTCTCAAGTGGTTG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CTTTGGAATCTGGAGTCCAGGAATGACCAGCTTGG
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TGTTTTGTCTCTAAACCAAGCGTAATCCCACCATA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	TTGTGCATGGATGCAGCCATCTCAGCCTCAGCA
GTGACAAACTACCTCTTCCCCGCAAGGGGATTGAAAC	CGAAGAATTCCACGGCACCCTTTAGCGGGATTTCA
GTGACAAACTCTGGAGCATACAGAATACGAGAACGGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087541914.1\|4934078_4936319_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_157679566.1\|4930221_4930413_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541918.1\|4938263_4939331_+\|zinc-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|376518
NZ_CP019636.1\|WP_087546274.1\|4930661_4932029_+\|TIGR03985-family-CRISPR-associated-protein	WYL	mkCas0075_WYL_CAS-I:CAS-III	gnl\|CDD\|274901
NZ_CP019636.1\|WP_087546273.1\|4928518_4929445_-\|CRISPR-associated-protein-Csx3	csx3	mkCas0115_csx3_CAS-I:CAS-III	gnl\|CDD\|370583
NZ_CP019636.1\|WP_087541908.1\|4924071_4926414_-\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl\|CDD\|274208
NZ_CP019636.1\|WP_087541907.1\|4923367_4924075_-\|CRISPR-associated-protein-Csm3	csm3gr7	COG1337_csm3gr7_CAS-III-D	gnl\|CDD\|224256
NZ_CP019636.1\|WP_087541919.1\|4943936_4944797_+\|metal-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224033
NZ_CP019636.1\|WP_087541909.1\|4926814_4927159_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541906.1\|4922114_4923371_-\|CRISPR-associated-RAMP-protein-Csx10	csx10gr5	cd09700_csx10gr5_CAS-III-D	gnl\|CDD\|131722
NZ_CP019636.1\|WP_087541911.1\|4927596_4928451_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|187833
NZ_CP019636.1\|WP_087541917.1\|4937615_4937924_-\|metal-sensitive-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197393
NZ_CP019636.1\|WP_087541910.1\|4927151_4927574_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538406.1\|4942718_4943282_-\|recombinase-family-protein	unknown	unknown	gnl\|CDD\|239737
NZ_CP019636.1\|WP_087541915.1\|4936585_4936828_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538405.1\|4940102_4941074_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|225806
NZ_CP019636.1\|WP_087541920.1\|4946941_4949737_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541916.1\|4936947_4937130_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541913.1\|4933653_4934070_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087541905.1\|4921707_4922118_-\|hypothetical-protein	csm2gr11	mkCas0063_csm2gr11_CAS-III-D	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087538406.1\|4942718_4943282_-\|recombinase-family-protein	gnl\|CDD\|239737	cd03768, SR_ResInv, Serine Recombinase (SR) family, Resolvase and Invertase subfamily, catalytic domain; members contain a C-terminal DNA binding domain. Serine recombinases catalyze site-specific recombination of DNA molecules by a concerted, four-strand cleavage and rejoining mechanism which involves a transient phosphoserine linkage between DNA and the enzyme. They are functionally versatile and include resolvases, invertases, integrases, and transposases. Resolvases and invertases affect resolution or inversion and comprise a major phylogenic group. Resolvases (e.g. Tn3, gamma-delta, and Tn5044) normally recombine two sites in direct repeat causing deletion of the DNA between the sites. Invertases (e.g. Gin and Hin) recombine sites in inverted repeat to invert the DNA between the sites. Cointegrate resolution with gamma-delta resolvase requires the formation of a synaptosome of three resolvase dimers bound to each of two res sites on the DNA. Also included in this subfamily are some putative integrases including a sequence from bacteriophage phi-FC1.	1.3966e-60
NZ_CP019636.1\|WP_087541919.1\|4943936_4944797_+\|metal-ABC-transporter-permease	gnl\|CDD\|224033	COG1108, ZnuB, ABC-type Mn2+/Zn2+ transport systems, permease components [Inorganic ion transport and metabolism].	3.74956e-65
NZ_CP019636.1\|WP_087541917.1\|4937615_4937924_-\|metal-sensitive-transcriptional-regulator	gnl\|CDD\|197393	cd10158, CsoR-like_DUF156_1, Uncharacterized family 1; belongs to a superfamily containing the transcriptional regulators CsoR (copper-sensitive operon repressor), RcnR, and FrmR, and related domains; this family was previously known as part of DUF156. Uncharacterized family 1, belonging to a larger superfamily that contains various transcriptional regulators that respond to different stressors such as Cu(I), Ni(I), sulfite, and formaldehyde, and includes CsoRs (copper-sensitive operon repressors). CsoRs form homotetramers (dimer of dimers). In Mycobacterium tuberculosis CsoR, within each dimer, two Cys residues on opposite subunits, along with a His residue, bind the Cu(I) ion (forming a triagonal S2N coordination complex, C-H-C). These residues are conserved in the majority of members of this superfamily, including this family; however, a conserved Tyr and a Glu residue that facilitates allosteric regulation of DNA binding for CsoRs are poorly conserved.	1.74336e-28
NZ_CP019636.1\|WP_087541906.1\|4922114_4923371_-\|CRISPR-associated-RAMP-protein-Csx10	gnl\|CDD\|131722	TIGR02674, cas_cyan_RAMP_2, CRISPR-associated RAMP protein, Csx10 family. CRISPR is a widespread repeat family in prokaryotes. At least 45 different protein families occur in prokaryotes only when these repeats are present. This family, a minor CRISPR-associated protein family, seems largely restricted to the Cyanobacteria. It belongs to the RAMP superfamily (pfam03787).	1.59599e-132
NZ_CP019636.1\|WP_087546273.1\|4928518_4929445_-\|CRISPR-associated-protein-Csx3	gnl\|CDD\|370583	pfam09620, Cas_csx3, CRISPR-associated protein (Cas_csx3). This entry is encoded in CRISPR-associated (cas) gene clusters, near CRISPR repeats, in the genomes of several different thermophiles: Archaeoglobus fulgidus (archaeal), Aquifex aeolicus (Aquificae), Dictyoglomus thermophilum (Dictyoglomi), and a thermophilic Synechococcus (Cyanobacteria). It is not yet assigned to a specific CRISPR/cas subtype (hence the x designation csx3).	5.46021e-33
NZ_CP019636.1\|WP_087541908.1\|4924071_4926414_-\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	gnl\|CDD\|274208	TIGR02577, thermophile-specific_DNA_repair_system, CRISPR-associated protein Cas10/Cmr2, subtype III-B. This model represent a Crm2 family of the CRISPR-associated RAMP module, a set of six genes recurring found together in prokaryotic genomes. This gene cluster is found only in species with CRISPR repeats, usually near the repeats themselves. Because most of the six (but not this family) contain RAMP domains, and because its appearance in a genome appears to depend on other CRISPR-associated Cas genes, the set is designated the CRISPR RAMP module. This protein, typified by TM1794 from Thermotoga maritima, is designated Crm2, for CRISPR RAMP Module protein 2.	2.21128e-42
NZ_CP019636.1\|WP_087541907.1\|4923367_4924075_-\|CRISPR-associated-protein-Csm3	gnl\|CDD\|224256	COG1337, COG1337, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.25632e-35
NZ_CP019636.1\|WP_087538405.1\|4940102_4941074_-\|AAA-family-ATPase	gnl\|CDD\|225806	COG3267, ExeA, Type II secretory pathway, component ExeA (predicted ATPase) [Intracellular trafficking and secretion].	3.78807e-53
NZ_CP019636.1\|WP_087546274.1\|4930661_4932029_+\|TIGR03985-family-CRISPR-associated-protein	gnl\|CDD\|274901	TIGR03985, hypothetical_protein_sll7078, CRISPR-associated protein, TIGR03985 family. Members of this protein family belong to CRISPR-associated (Cas) gene clusters. The majority of members are Cyanobacterial.	1.09463e-131
NZ_CP019636.1\|WP_087541911.1\|4927596_4928451_-\|hypothetical-protein	gnl\|CDD\|187833	cd09702, Csx1_III-U, CRISPR/Cas system-associated protein Csx1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Protein of this family often fused to HTH domain; Some proteins could have an additional fusion with RecB-family nuclease domain; Core domain appears to have a Rossmann-like fold; loosely associated with CRISPR/Cas systems; also known as TIGR02710 family.	0.0045247
NZ_CP019636.1\|WP_087541918.1\|4938263_4939331_+\|zinc-ABC-transporter-substrate-binding-protein	gnl\|CDD\|376518	pfam01297, ZnuA, Zinc-uptake complex component A periplasmic. ZnuA includes periplasmic solute binding proteins such as TroA that interacts with an ATP-binding cassette transport system in Treponema pallidum. ZnuA is part of the bacterial zinc-uptake complex ZnuABC, whose components are the following families, ZinT, pfam09223, pfam00950, pfam00005, all of which are regulated by the transcription-regulator family FUR, pfam01475. ZinT acts as a Zn2+-buffering protein that delivers Zn2+ to ZnuA (TroA), a high-affinity zinc-uptake protein. In Gram-negative bacteria the ZnuABC transporter system ensures an adequate import of zinc in Zn2+-poor environments, such as those encountered by pathogens within the infected host.	4.48836e-85

>NZ_CP019636.1|WP_087546274.1|4930661_4932029_+|TIGR03985-family-CRISPR-associated-protein
MRLWVLLNKLYSEEHWASSLPKIFTYAQLRDRLFSPTHSRSDKLSASQVVNSCQDLSCICHKSLQDWVFHTDTYLSKSEWQQAVVQLTGISTTDLEQQLQQYPFATVHRSIREDLKYLTQQGWLVAHSQGQYSCRPFQELPTPPTAISPAPNFAQLSVPQTWELLRVLESISFVQPNLEVVVRDLWEQVTDIATPSHKLKTEPQQRIFIHLDYILSDEMQDRVDTHQEQIEQLWHRPPGGVVQFEYWLASEERKVNVTVYPVCLHYLRRAKYLSAYGIDPQGKIDWHNYRLDRIASPHLQVLAWGDPSVPKPLKELWRTGQLPQPEEVKQHLDTAWGFNFYLKRELLILRFPPAFARWYVDDTVRHPTFQPVDYEQLPKLIATSVLSPVEQKQLLEIIKQRDKNDRYYQAWIRTGDINVLMRLRDWRPNGEVIAPLSVRHRLKEEAIQELSNYQI
>NZ_CP019636.1|WP_157679566.1|4930221_4930413_+|hypothetical-protein
MWSSVLSEPVVDYLFPARGRKLQQHHGIQILRLCRGRRLPFPRKGTETHERARQVLRTVFQEL
>NZ_CP019636.1|WP_087546273.1|4928518_4929445_-|CRISPR-associated-protein-Csx3
MNPSHPSIRLHLSHHENPQGLKYQQLTIELTRKDRIIYPEEIADLELPSGIDTTCGVVISGRAPIWLHGYLMYELHPTAWVAYYEPRMYSAIVAATQTRQVKIGQVIPLEQKGDGTLCAGLMIVGPPDSGKSVLSHTLFKALLADHPDIYLQRANWDGEGNYVLESVFTEEQQEAFKAANKGGLTERFFPYHAQAILQLRRQKALVIVDVGGMVQPEKQPILEACSHYIIISSKPEAIPAWHEFCRDSGNLKPVAVIHSTLSECEIIHQQEPYVEITCGPWVRGQATEVPVSLLECVRPIVKHLVAEG
>NZ_CP019636.1|WP_087541911.1|4927596_4928451_-|hypothetical-protein
MLGPKHKRYVKLENIFSPRSPLEFLGFSLVGVIINLLSGAHPAGFIGVVVLFLCWWILDVWRSKNLSKQLGFSITKKSPKAAKGLILLLSPYSPQSMALKDEQKLKPLITKILTMPHDTLSEADFNDIDLFNSNLLPQIKAVEYHWEQSTLDDVWLISSESYENVRGSEETAQILEKYLRFHYGKVLNIHSQGLVVKDWDYKTLWQLGEDIFRRSDYKEQAIVVDITGGTKMMSVALAMVCIPPNRQMQYMDSQRDWQGNPLPKGEMKPVVIDINPFLYPFLED
>NZ_CP019636.1|WP_087541910.1|4927151_4927574_+|hypothetical-protein
MIKTTSDTQTPEIKRNYISQLLEQLTVDYQNTKQERKEITALYPAGDEEFSILEEIELLTVDIRGYASQIQARGSIENEQQAIERLQKMRVFDIPVITEFYFTSNRSYRQMKAYLQMLDYLRLLIIEYLQIYQISQPQSA
>NZ_CP019636.1|WP_087541909.1|4926814_4927159_+|hypothetical-protein
MYDEPPADPFFAQLCEGYTEAEVAEIQQYMAEWDASTYISVAQTIVDHASRKEFDPLKYLRKAHNFNKKRAARIPKSGYRQDGSAVYRKGNEYLIVRPDKLGIEKIVTYGLNDD
>NZ_CP019636.1|WP_087541908.1|4924071_4926414_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MTNSQHSITTAISWCLAWGDKREPNFDIAVLQQMRQALNDGKDVPEKVRSLVEQVKQLQGIDKDYFPETLDELKSKYPELCNQTTRIGLVYGGATKIKQYVFESSKIQDIRGASALLDRINLIDLPAFFNKNPQSSNSYTIQCNQVRQWLDQKFSAGYKLSQILIPELIIYSTGGNILAFCPAAFVDDLANAIEKRYTEETLTANSCAVGEKFRLLELRFGLLREPIENMQWLDWYYREYDKPLVQAYFGYPTNDSEKLEAFKNRKSFNELTTKLAILFNQRRSGHDFSNRPSRRYPPMFETHPYLMRDEGERRSAVMIVQPPELPKKSHFSEASARKHLVGYRAKKGKPDLPEWYKNSHLTWESIRVEGWVDKFNSFLNKNPNLKQKYYANLKHDNIEIPQNLSHIANASKDFIAYIYADGNNMGGYIQKIRTSQKYQEFSQDVELATEYAVYQALAENLHPHELRNFKDEESTLSNGDLVHPFEIITIGGDDIILIVPANKALQIAQMIGERFEKILLKQVPLVENSTAEEKINGCYRIKTSDKPTDLKKCHRYKPTEATPSQCELSTSIGVLITAYNTPIYYAKGLTEQLLKSAKDRGKKLKEAGYCGGTVDFLTMKSVTMISSDIKEFRQQALTKNLKSKLKLYAAPYTLHELGGLITAIKALKKAHFPKSQLYQIRSLLERGKHTAILNYRYFRVRLKQGKAELQTDFENAWCQPKDENNGGNLAPWMYDDGKIDPKNLEDPFYETIWREMVELYEFIEIPDSELSELSSVGTEL
>NZ_CP019636.1|WP_087541907.1|4923367_4924075_-|CRISPR-associated-protein-Csm3
MINLQELSNPITSYQITAVIDTALCVGAGGSSGSLADKPIVRNSEGNLLIPASQLKGRLRHECEKIARGLCWHICYSPNPQTMCPQRAGLTGNFERTEYHVSGYEGHHHCLICQIFGNPVLPSRVIFDDLICTEDPDNLPEVLRPGVTINRRRCTAEEQKLYFLETSPTNAQLRFTGHIHLSRVPVYAGALILAGLRHINALGGSKSAGLGWLHWQFPNLPVEQAAWNFLARGVQ
>NZ_CP019636.1|WP_087541906.1|4922114_4923371_-|CRISPR-associated-RAMP-protein-Csx10
MKRIDLEIKALSPLAIGRQKPGGSISEAESYIPGSVIRGAIAAHILNQANTSITDGDNFYELFLGESPAIFQNAYPATIEEGKQTRGQSEVKVLPATALSSKIKSGFKSKPNDPKHNGVFDTLIDRFCAEGYGQLYDPNCPTERRVDGDRVDNFTGFYSQLKEKYYGHSVTSRLLTRTGINRRRATSEERVLYSIEVLNESQDNRQISIIYTGAILVADELAESLQEFIKNHKEDLRLGGATSRGLGRVKITPKPPVELKPKVTDKIKQFNDKLRQRWCQWKNIFGNPIKDLLENRDYFTLDLQADAILIDNWRRTTVISSEMLQQFTAVSDSSLQLHAAYSSYDYRSGWNSAWGLMKDMELITNKGSVYLFSTAEKDLWSKALEDLEVKGVGDHTCEGFGQVQICNPFHLVMREEAV
>NZ_CP019636.1|WP_087541905.1|4921707_4922118_-|hypothetical-protein
MSLPIESKTELKVQKGIRQVEDDLVIWIQEALDNANYGDLEESQFRNLVRVSDTTESVEAIKNFIRYQVGRDRKWGRGEDSLAQNIIEDIDNNIRESAQTIAEYCQTDFKPIWLELIRRYLGYGARYLKYLRDGNV
>NZ_CP019636.1|WP_087541913.1|4933653_4934070_-|hypothetical-protein
MEVYLNTQVDLNSAIDQVWRSLSERNQQWKQRQEAAIAQAKQILAQQFQQDLTEVLPSEIQNSLGIQIKQSLDISDISADFEFMDSPFSIKRIWLSDSMYWRIVHLKENIDCQPENLKNQLLRELAKLKNQSNTESQS
>NZ_CP019636.1|WP_087541914.1|4934078_4936319_-|hypothetical-protein
MPSYTRNVKRDNLVFVPVNPKILYGFKTKDLTSISGVSAADIAPLGHLTATAASGRAGAILVVGANAPKPPRVTKRISAAAAGVQQSVSTFCATSSLAGALAAGWNVAKPGRGVLTRNASASRGTLTAIATLSNGARYCFPMNKADFDAHGAALGLESAATITNQGERDSLVRGTRLPRPGRASLEVAGGGTFVSFFSSSFSGELGKNNFHQLSEEVILNGAAPAAADIVRESLSSELTRSQIGRAGVRVFRALQTTQTDSNGNIIRWLWNAGNQFFGLIGAAFKIIGVSFTALWALVVSTVQYVWNFNWNISDRELDQQLQNSLNVLAALLGGTVGNSIGYLACGVLPGAYIFSLNEPLGAHVLANVAEEMAEEFLANVNNLIRYSFISGVQALLMWGFRNVRKLIKSNIAFVQAVFGDKAARAVQAWGQPNSKPWSFALALNNAVESIPNTAVQNFVEEFLEEAWEGCVEAGYVVANSLDAYIAQQKLASQQQLILGQQRYVEVQPDRTNERERIILAGPEQPLKAALVQTLSNYQLIENRDVGQLVGMPADDYLRAKPQSIRLVITFSSVSSPPWKAAAGQRLVTATYAVPDVKRSKCDWETIKQACGGRNGYLWGRYRATGILSNGRQMQVMGATGDEAEDRLRALVALSEATLVKKPTISEDRSEDASGSYTKQPTRIYPAFCTIMNQYQVPGARGSSIRLNGGEYMRRQDKILLWTEEKPFGTDELIAELLRKPGAEEHT
>NZ_CP019636.1|WP_087541915.1|4936585_4936828_+|hypothetical-protein
MELKAFPLLDTRCKRLMLRRKHRVGKRGRQTYHYRPQQRLINRLAAQLQMPPQAVRQQIAQERLYLLRQMYGPDIGPQDV
>NZ_CP019636.1|WP_087541916.1|4936947_4937130_+|hypothetical-protein
MSLQELKEQIYKLSVSDHLTLVSAIIQSLQDAPQAEDWQYLVTRPHSWRKQLYIKVELTH
>NZ_CP019636.1|WP_087541917.1|4937615_4937924_-|metal-sensitive-transcriptional-regulator
MDSEEKTLPNLQHSYSEASLQDLMKRLSRIEGHIRGVKNMVESSRPCPDVLIQIAAVRGAVQQVGRIILNEYLKESVARTTKEGDIKTEIAALKTVLDRFLT
>NZ_CP019636.1|WP_087541918.1|4938263_4939331_+|zinc-ABC-transporter-substrate-binding-protein
MKTSALLLVFSLTLTACNAPQNTAVSPTPSQSTATVQPVQNQTKSKTLVVTTVAPLTNIVSNIAGERLEVKGIIPEGTDSHTFEPRPSDTDLLSKANLIIVNGLHLESPTEKLAKASKPQQTNIYELGSNTITESQWIYDFSFPKEKGDPNPHLWVNPKYAEAYAKLAAKQLTQLDPEGKDYYAKNLNNYLQRLDALDKVTREVVASIPAKNRKLLTYHDSWAYWAREYGFQVIGAIQPSDFKEPSAQDVAKLIEQIRKLGVPAIFGSEVYPSKVEEQIAREAKVKTANTADDELPGTGSANAIENTNPQHTYIGMMANNLRIIAENLGGNPKLVDKLNTTNVVGPTATTATTTQ
>NZ_CP019636.1|WP_087538405.1|4940102_4941074_-|AAA-family-ATPase
MLTEVMEFYGLVKEFRRAGYYETDHLRQLFKEIKAAIPQGKMIAVTGVVGCGKTVTLRRLQEALKKEGKILVSKSLSVDKNRATLPTLIAALFYDLSSDKEVKISTQGEKRERELQELIRKGKKPVALFVDEAHDLHSSTLTGLKRLIEVVEDSGGILSIILAGHPKLKNDLRRPMMEEIGYRTVIFSLDSIGGSQRQYIEWLLSSCTKEGTLLENLITAEAIDLLCTRLRTPLQIEMHLSLSFEEAHRMGEAIVTLSIVESILSKQIDDLEPTLTRHGYNVKSLSEQLNAKPSEIRSLLRGQLDPTRTRELQEQMLAAGLPI
>NZ_CP019636.1|WP_087538406.1|4942718_4943282_-|recombinase-family-protein
MLIGYARVSTDDQNLNLQKDALKQAGCSRIYEDRLSGAGVARPGLTKALEAARAGDVLVVWRLDRLGRSLKDLIQMVETLSERGIELHSLTEALATTSTSGKLIFHLFGALAEFERNLIRERTQAGLTAARARGRKGGRPKALDAPKRQLAIKLYNERQYTIEEICRIMGISKPTLYSYIAKAQGTP
>NZ_CP019636.1|WP_087541919.1|4943936_4944797_+|metal-ABC-transporter-permease
MEFLLKPFQYEFFSRAVAVGMMAGLLCGVMGVYIITRRMSYIAHGLSHAILGGAVLSYVLGLNFYIGSGIWGFAAALLIQYLTGRKVYSDAAIGIVTTASFALGVAVISTYRKFSQNFEAALFGNVLGVSPSDLWFVTAVTIVILSLCFFFYRPLLFWCFDREVAQVHGVPVVAMDTLFALMLATLLVATLNVLGVTLIISAVVIPASIARLLSDRFGSVIVISGVLGAAIAFIGIYLSYYLDIASGASVVLLSTLVFGCVLLWKSIQSRRKRYVPPLSSQHYQDY
>NZ_CP019636.1|WP_087541920.1|4946941_4949737_+|hypothetical-protein
MLHKLICGWQNINLSLLTILLTSIFMFDRVDAKNQAYTNVSVLASTSELEINTDSHSRKSLLSRQPQIFKKYYIVQKLNQEPIKFFPDINIPELPKNTLPESNTNHLNPNNSNRQNQTPDLNNKNLELLILDSLTNSSNKYPWIVYPTDEFRFSSVFNPTKNTNYIDFSFDLKSHEPIFEYLVFASFPKQKQFYWSLPGNRIVMETQGWQGGIFDQGQSTKIESRQLIMLTQKLWGMQAVSVIPQSFKDLTGEIDTNNFSIQSIAAEAIIPPGFPTPKIIIDNGNSNSTIKNIPRISNLGTASTYSPKGGESLFGFLDANNAPLLLQTFPTSNLQPLLEAGNLSRGTIISQDTLAKIGFYWGNPFTGEATRFQPPMTSKPGLKIGQIGQFDNWSLLNILINPFLSAKERNLYYLNSLYWVPLGQRISNITLNQRQENYHWQRFYLSRPHNRTLLEYDPVKAQGTYTNIFSNPGISLSLLANQGEIDELQSANTTLGMLMGGIFEFIHLPELEQSLQEAKKRFAQKENLTDLNLKATPDQIRQINQLLNRTLLLGNRNSRLEQVSGTLTFPSKITPNSSNILQIRTGNYQRAVQFADGNLTWIKGQTFISRADISNTSFGPLTFIGIPVPLEQTSILPSNRTAVAQVTLTDSNGQQFVQNWSLADTTEVPMNIRSFAIAFDHIELSQANQLITKSQTFNGHLFLPTLEVLWAGSSGNWNYSINSGIWFNLNSNSAFNVANNSLGLSEPTVGVYANGALSYIKTHVEVDTKGQIQAIISHIPSFRFYWNSAANSQNPTYLNFSYSFSRQDHNLNYSLAPAIIFFYNQGQLTPAGFLQGKLLLNQGLELSNFLQIGDHFLYKFTGIQKLNQNWSVGAYLQNFTEINQVIRTNNNDLSYGLITKHTSANGNNFWESQIGMNGDNFEVRFQRGWRF

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Crispr_ID: NZ_CP019636_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_17

5170178-5170301

Orphan

Consensus_repeat	Method
TGTAGGATGGGTTAGCGAAGCGTAACCCATGCTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_17

>merge|NZ_CP019636|17|5170178-5170301|CRISPRCasFinder
TGTAGGATGGGTTAGCGAAGCGTAACCCATGCTGTCCAAGCGATTGATGCGAAATGTAGGATGGATGCTGTCCAACAGATAGATGCAAAATGTAGGATGGGTTAACGAAGCGTAACCCATGCTG

>NZ_CP019636|17|16|5170178-5170301|CRISPRCasFinder
TGTAGGATGGGTTAGCGAAGCGTAACCCATGCTG	TCCAAGCGATTGATGCGAAATGTAGGATGGATGCTGTCCAACAGATAGATGCAAAA
TGTAGGATGGGTTAACGAAGCGTAACCCATGCTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087546288.1\|5178395_5179466_+\|transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP019636.1\|WP_087542098.1\|5167196_5168120_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542092.1\|5160217_5160580_-\|phage-holin-family-protein	unknown	unknown	gnl\|CDD\|224861
NZ_CP019636.1\|WP_087542103.1\|5181678_5182011_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542095.1\|5163853_5164945_+\|4-hydroxyphenylpyruvate-dioxygenase	unknown	unknown	gnl\|CDD\|273528
NZ_CP019636.1\|WP_087542100.1\|5170479_5171679_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366526
NZ_CP019636.1\|WP_087542102.1\|5177615_5178077_+\|response-regulator	unknown	unknown	gnl\|CDD\|381108
NZ_CP019636.1\|WP_087542105.1\|5184112_5184352_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542094.1\|5162191_5163076_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542097.1\|5166309_5166678_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542101.1\|5176035_5176641_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP019636.1\|WP_087542096.1\|5165002_5166160_+\|homogentisate-1,2-dioxygenase	unknown	unknown	gnl\|CDD\|226039
NZ_CP019636.1\|WP_157679596.1\|5181267_5181471_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_157679590.1\|5166659_5167091_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|270351
NZ_CP019636.1\|WP_157679592.1\|5171660_5171969_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542093.1\|5160805_5162125_-\|fumarylacetoacetase	unknown	unknown	gnl\|CDD\|215461
NZ_CP019636.1\|WP_087542091.1\|5159439_5160147_+\|photosystem-II-biogenesis-protein-Psp29	unknown	unknown	gnl\|CDD\|371440
NZ_CP019636.1\|WP_087546287.1\|5158583_5159180_-\|chorismate-mutase	unknown	unknown	gnl\|CDD\|368789
NZ_CP019636.1\|WP_157679594.1\|5176681_5176867_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546013.1\|5179753_5181133_+\|IS110-family-transposase	unknown	unknown	gnl\|CDD\|376564

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087546288.1\|5178395_5179466_+\|transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	3.51627e-07
NZ_CP019636.1\|WP_087542092.1\|5160217_5160580_-\|phage-holin-family-protein	gnl\|CDD\|224861	COG1950, COG1950, Predicted membrane protein [Function unknown].	2.075e-20
NZ_CP019636.1\|WP_087542095.1\|5163853_5164945_+\|4-hydroxyphenylpyruvate-dioxygenase	gnl\|CDD\|273528	TIGR01263, 4-hydroxyphenylpyruvate_dioxygenase, 4-hydroxyphenylpyruvate dioxygenase. This protein oxidizes 4-hydroxyphenylpyruvate, a tyrosine and phenylalanine catabolite, to homogentisate. Homogentisate can undergo a further non-enzymatic oxidation and polymerization into brown pigments that protect some bacterial species from light. A similar process occurs spontaneously in blood and is hemolytic (see . In some bacterial species, this enzyme has been studied as a hemolysin. [Energy metabolism, Amino acids and amines].	2.50999e-157
NZ_CP019636.1\|WP_087542100.1\|5170479_5171679_+\|hypothetical-protein	gnl\|CDD\|366526	pfam01231, IDO, Indoleamine 2,3-dioxygenase.	1.6348e-109
NZ_CP019636.1\|WP_087542101.1\|5176035_5176641_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	3.37581e-18
NZ_CP019636.1\|WP_087542096.1\|5165002_5166160_+\|homogentisate-1,2-dioxygenase	gnl\|CDD\|226039	COG3508, HmgA, Homogentisate 1,2-dioxygenase [Secondary metabolites biosynthesis, transport, and catabolism].	3.85327e-64
NZ_CP019636.1\|WP_157679590.1\|5166659_5167091_-\|hypothetical-protein	gnl\|CDD\|270351	cd13633, PBP2_Sa-PDT_like, Catalytic domain of prephenate dehydratase from Staphylococcus aureus and similar proteins, subgroup 4; the type 2 periplasmic binding protein fold. Prephenate dehydratase (PDT, EC:4.2.1.51) converts prephenate to phenylpyruvate through dehydration and decarboxylation reactions. PDT plays a key role in the biosynthesis of L-Phe in organisms that utilize the shikimate pathway. PDT is allosterically regulated by L-Phe and other amino acids. The catalytic PDT domain consists of two similar subdomains with a cleft in between, which hosts the highly conserved active site. In gram-postive bacteria and archaea, PDT is a monofunctional enzyme, consisting of a catalytic domain (PDT domain) and a regulatory domain (ACT) (aspartokinase, chorismate mustase domain). In gram-negative bacteria, PDT exists as fusion protein with chorismate mutase (CM), forming a bifunctional enzyme, P-protein (PheA). The CM in the P-protein catalyzes the pericycle isomerization of chorismate to prephenate that serves as a substrate for PDT. The CM and PDT are essentail enzymes for the biosynthesis of aromatic amino acids in microorganisms but are not found in humans. Thus, both CM and PDT can potentially serve as drug targets against microbial pathogens. The PDT domain has the same structural fold as the type 2 periplasmic binding proteins (PBP2), many of which are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. 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.	0.00523154
NZ_CP019636.1\|WP_087542102.1\|5177615_5178077_+\|response-regulator	gnl\|CDD\|381108	cd17557, REC_Rcp-like, phosphoacceptor receiver (REC) domain of cyanobacterial phytochrome response regulator Rcp and similar domains. This family is composed of response regulators (RRs) that are members of phytochrome-associated, light-sensing two-component signal transduction pathways such as Synechocystis sp. Rcp1, Tolypothrix sp. RcpA, and Agrobacterium tumefaciens bacteriophytochrome response regulator AtBRR. They are stand-alone RRs containing only a REC domain with no output/effector domain. The REC domain itself functions as an effector domain. Also included in this family us Methanosaeta harundinacea methanogenesis regulatory protein FilR2, also a stand-alone RR. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	5.21266e-32
NZ_CP019636.1\|WP_087542093.1\|5160805_5162125_-\|fumarylacetoacetase	gnl\|CDD\|215461	PLN02856, PLN02856, fumarylacetoacetase.	0
NZ_CP019636.1\|WP_087542091.1\|5159439_5160147_+\|photosystem-II-biogenesis-protein-Psp29	gnl\|CDD\|371440	pfam11264, ThylakoidFormat, Thylakoid formation protein. THF1 is localized to the outer plastid membrane and the stroma. THF1 has a role in sugar signalling. THF1 is also thought to have a role in chloroplast and leaf development. THF1 has been shown to play a crucial role in vesicle-mediated thylakoid membrane biogenesis.	7.93078e-133
NZ_CP019636.1\|WP_087546287.1\|5158583_5159180_-\|chorismate-mutase	gnl\|CDD\|368789	pfam06206, CpeT, CpeT/CpcT family (DUF1001). This family consists of proteins of proteins belonging to the CpeT/CpcT family. These proteins are around 200 amino acids in length. The proteins contain a conserved motif PYR in the amino terminal half of the protein that may be functionally important. The species distribution of the family is interesting. So far it is restricted to cyanobacteria, cryptomonads and plants. It has been shown that CpcT encodes a bilin lyase responsible for attachment of phycocyanobilin to the beta subunit of phycocyanin.	1.79875e-75
NZ_CP019636.1\|WP_087546013.1\|5179753_5181133_+\|IS110-family-transposase	gnl\|CDD\|376564	pfam01548, DEDD_Tnp_IS110, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family includes an amino-terminal region of the pilin gene inverting protein (PIVML) and of members of the IS111A/IS1328/IS1533 family of transposases. The C-terminus is represented by family pfam02371.	7.7599e-20

>NZ_CP019636.1|WP_087542098.1|5167196_5168120_+|hypothetical-protein
MTQTLTTTPKHLTISSRIEERSRRGELTQQQVDDFQDFLAEVDQEFLQHRIIINNSYTRWFRNGNVTDEELRHFIRQFSVFSNQFLIAALLKVINSPTLQQSRATREILLNELGVIYRKVGHSSDSKIVPTEEEKDREGDPELVSTEGTVDGGICRFRAAHFEWLIGVAEGLGLHYEDIGKRKHGRPTTLHFCDELQRLYGSDDPHIAEGASFAVENWAAAGFWQELEDGLTRIKQTRYPHLHLAFFSWHNRVEGQHAGHTLEELEAVYFQPDFDRDKFIQGGREILDAIAVFWDGLDQDRLNKVYM
>NZ_CP019636.1|WP_157679590.1|5166659_5167091_-|hypothetical-protein
MTYLQTIYLLRAVLKPKTRSIEPSFELDLDSPRGLHHPQALGTCRQYLRSWFCHFPGFRAPHDTLISEIILLFLDLVCVRNSGYVFTRLRHRAASIVIRPRSGVLSAKRLNPICRTPCLGLSPVALISITPRTKESQRWARKD
>NZ_CP019636.1|WP_087542097.1|5166309_5166678_-|hypothetical-protein
MGKKRLKNVPILYEGIKKKRAIGLTDTAYQNLQEAAAVEKLSLSEFVETWARQLKLQRIHESALKEGFQRQMLHLGKHARCHNAGNPRNALAPQDRTGSSVGVWCPHTFKVWAFCFHCCKIF
>NZ_CP019636.1|WP_087542096.1|5165002_5166160_+|homogentisate-1,2-dioxygenase
MTYYYKLGNIPHKRHTQFRQPNGSLYHEELIGIHGFSGIQSLLYHLRPPTQIQKILLQTTVDIPYEETDSLRPRHLRTANVELGGDAVEARIPLMANMDICISVARPQLSMSYWYRFAHGDEVIFIHDGTGILESQYGILRYHPGDYLVIPCGVLWRIIPDANTEQRMLVIEANGHIEPPARYLNRYGQFLEHAPYNERDIRPPDELLTHDEEGEFEVRVKARDRITSYLYHHHPLDVVGWDGHLYPFAFNIEDFEPITGRIHQPPPVHQTFEAPGFVLCSFVPRLFDFHPLAIPAPYNHSNVDSDEVIYYVAGNFMSRKGIERASMTIHPSGIPHGPHPGMYEGSIGKERTDELAVMIDTFRPLQLTKYALALEDKDYAYSWIA
>NZ_CP019636.1|WP_087542095.1|5163853_5164945_+|4-hydroxyphenylpyruvate-dioxygenase
MSDFCPIKRFDHLEFYVGNARQAAQFYSKFFGFTNTAYRGLESGSREVASYVMQQGDICFVLSTALFPEHPISQSVLKHGDGVAIIALEVMDAVSAYKETTKRGAVGAIEPTEEEDGYGVFRYAAIHAYGDVLIKFVERSDYSGVFAPGFMPQHHAHNSNSVGLHTIDHVVGNVELGAMDQWVQFFADTMGFNLLVHFDDETISTEYSALMSKVMQNGTGKIKLPINEPAKGKRKSQIEEYLEYNNGSGVQHIACATNNIIETVSQLKTAGAEFLHVPRTYYENLEERVGKIDEPIEQLQELGILVDRDEDGYLLQIFTQPVQDRPTLFFEVIERHGSQGFGEGNFKSLFEAIEREQALRGNL
>NZ_CP019636.1|WP_087542094.1|5162191_5163076_-|hypothetical-protein
MIASVQALLASIVDYAGLFPPAKLDLRQAMTNYIGNQLTPYAWMQNRFVLPVSRLNEFEALLQIFLAKEDNPRQWSLSLIVPEDVEAVIQQLKLLNNRNDITVTALEFPPLPPREIERILPHLPMGVDAFFEIPLTGLEAYLRVLQHTGAAAKVRTGGITVDAFPSFEELCQCIFSFAEAEVPFKATAGLHHPLPGNYRLTYEPDSPTSVMHGFLNVAVLAALVYWQKVTLPEALEVLQDSTSDGFQFTAEALTWRDYRLESVQIQQARQRFFRSFGSCSFQEPVDELKELKLY
>NZ_CP019636.1|WP_087542093.1|5160805_5162125_-|fumarylacetoacetase
MSRPIDTTHDPNLRSWVESANHKDTDFPIQNLPFGVFRPRSSAEPSRIGVAIGDQILDLSLCCQLGLLQELPEQLQAACAAPNLNQLMAMGREATSMLRRHLSQMLRSQEQIPPSADEILVPMSEAELLLPAHIRDYTDFYASIFHATNVGKLFRPDNPLLPNYKYVPIAYHGRASSIVPSDTAIKRPKGQIKKPEAPAPSFQPTQMLDYELEVGFLIGAGNELGLPIPIDYAEEHVFGLCLVNDWSARDIQAWEYQPLGPFLAKSFATTISPWVVTMEALAPFRCPAFERAEGDPLPLPYLSSSDNAKFGAIAITLEVLLCSVQMRTARMEPFLLSRGSFQQMYWTVAQMLTHHSSNGCNLSPGDLLASGTVSGTEKTSQGCLLEMTQRGVQPVKLPTGEIRSFLLDGDEVILRGYCEKDGYARIGFGECRGVVLSAG
>NZ_CP019636.1|WP_087542092.1|5160217_5160580_-|phage-holin-family-protein
MNLGTLLIVWVVTAISLYIISKLPIGVEIDTPGKAFISAAILGIVTAVVRPILRLAFAVPNILTFDLLSGFFTFIISVVCFGLAAWLVQGFRLRFGIWSAIIGAFALSVISSLIYKLLGV
>NZ_CP019636.1|WP_087542091.1|5159439_5160147_+|photosystem-II-biogenesis-protein-Psp29
MNNVRTVSDTKRTFYNLHTRPINTIYRRVVEELMVEMHLLSVNVDFSYDPIYALGVVTTFDRFMQGYQPERDKESIFHALLQAVEEEPQRYRQDAQRLQALAASLSPSELIAWLSQETSSTRDPDFQGSLQAIANNPKFKYSRLFAIGLFSLLEQSDQELVKDEKKRTEALKTIANGLHISDDKLNKDLEIYRSNIDKMSQALTVMSDMLLADRKRREQRSQQSSTTVAPPTTNE
>NZ_CP019636.1|WP_087546287.1|5158583_5159180_-|chorismate-mutase
MTFSPQLLALANYLAGEFDNREQAVAEPIWYVHLRLWHRPVPLFQEDSLTIFAEQANILKLDRPYRQRIIRLMQGSGSDASLKVQYYKPKNPSTLVGAGCNPGLLKTLTPDDLEFLPGCVLNITNQVLAPNSYQFTATPPPDTHCSFTVGSDVVQVSLGFEVSDGKFLSYDKGIDSTTGKATWGAILGPYCYTKREQY
>NZ_CP019636.1|WP_087542100.1|5170479_5171679_+|hypothetical-protein
MTRINLEEGSVNALKLEDYDVSQESGFLTTHSPAKVQLPESFWQVQAYAALLPKYMSTGKIRQGIKNLSEVDVERETLDEMQLRRVMQVYSYLTHAYVWGEPTSAKVLPRNIAVPFYRISQSIGRPPVLSYASYALDNWIRFNETEPIEIGNIMVSQNFMGGLDEDWFILIHIEIEAKAAPALAAIPRILEGIAQDDTSTVISALENIKKAWTNINTTMSRMPEACDPYIYYNRVRPYIHGWKNNPALPEGLIYEGVEAYGEKPQQFRGETGAQSAIVPTMDSLFKITHEHDPLWEFLREMRDYMPPKHCTFVEEVEKRSTLRDFVKNCMDTVPKLKDLYNECVSLIENFRTQHLLFAARYINQQTAKSNNDTDIGTGGTPFMQYLKKHRDEAAQHLLK
>NZ_CP019636.1|WP_157679592.1|5171660_5171969_-|hypothetical-protein
MSSVDYSVLSANYSASSVNYSVLSVDYLALSVDYSVLSANYSVLSVDYLASSVNYSVLSVDYLASSVDYSVLSVDYLALSVDYSVLSVDYSVLSVDYYFKRC
>NZ_CP019636.1|WP_087542101.1|5176035_5176641_+|TetR/AcrR-family-transcriptional-regulator
MTDHSPSPKDVSHSGRSRILDEAEALFRTRGGYNAVSMRDIACKVGIRQASLYYHFPSKEQLFVAVTERMFERHRTGLQQAIEQAGDDLKAQLDSVSGWFLSQPPMHFLSMIHMELPLLGEDNIKRLSVYSQECVFEPIRQLFAQAQERGEIRDDVRPKLLTGFFLSCIESVPYVRSFPDTASSKAIVNEVISVLLDGIKP
>NZ_CP019636.1|WP_157679594.1|5176681_5176867_+|hypothetical-protein
MSTHAAQTIDALRLRLTQRQVLQHGEPSEVCPEGNPPRNFSPQRTGSLTKNSVRLLSLFYL
>NZ_CP019636.1|WP_087542102.1|5177615_5178077_+|response-regulator
MANLEPITILLVEDNLPELRLIQLAIAKANLPISFQFAEDGSEAVSYLLGEGEFADRERFPLPQLIVTDIRMPLMSGLELMAWMKQQPQLQNLPIVAMVHSASPREVSQLESMNVTHFFKPIFINDWQEKMKQIVSLLPCFVDSHLAPNRTNP
>NZ_CP019636.1|WP_087546288.1|5178395_5179466_+|transposase
MPTQYQKDNLDTMMGLFLEAQGHPLPEHSQTKSPSALSRFLNMNPWSTKDMIRIVRSHVLETVSKVLSASGKGRRPFLQVIIDLTTLEKRGKFKEFEDLIRVYNGKRGLHIVVVYLVVGKWRIPWNFRVWRGKGTPSPAQLGLKLVKRLPKYLTERFQVIILADTAFGSVEFLDGVRKFRYHAVTGVAINRKLVDGRVLRHLHKQGQQVHLVGLKFPVTVSWYYLKRDKGKLEKRFVLSTRPIKASTLKWWGKRRWQIEGWFKTAKHRFGLHRFGQGSLLGMYRWLILSLTAYLIAHWTYLHIQSASPPDWGQAAQTALESIFPQIVVSLLLLNIERLAPLARSCGFDIYISRCKM
>NZ_CP019636.1|WP_087546013.1|5179753_5181133_+|IS110-family-transposase
MKKQEQPIAAEQRNLPVINPNAAGIDIGADRHWVSVPVDRDSENVHSFACFTAELYAMADWLKQCGIETVAMESTGVYWIPVFQVLESRGFEVKLVNAHYVKTVPGRKTDVLDCQWLQKLHSYGLLSGSFRPDDQICVLRSYIRQRDNLIKSACVHVQRMQKALTEMNLQLHRVISDITGTTGLSIIKAIVRGERNPLTLAALKDGRIKASCEEIAAALTGDYRDELIFILQQELQLYEFYQTQILAVDAQIEQCLASFADRVDVTKKPLTKPKRRGKKQPGNAPQFDLRTHLYRISGVDFTQIQGFGALTVLILLSELGLDPTRFPTVKHFTSWLGLCPGSRVTGGKVKSSQTRSVVSRAANAFRMAAQTLCRSNSALGAYYRRMQAKIGAPKAITAAAHKLARIFYRLWTSGDKFIDPGVDAYEQQYRERVVNNLKKKALTFGLELIPISDSTQCVS
>NZ_CP019636.1|WP_157679596.1|5181267_5181471_+|hypothetical-protein
MTYLQTIYLLRAVLKPKTRSIEPSFELDLDSPRGLHHPQALGTCRQCLQSWFCHLPGFRAPHDTLIC
>NZ_CP019636.1|WP_087542103.1|5181678_5182011_+|hypothetical-protein
MGKKRLKNVPILYEGIKKKRAIGLTDTAYQNLQEAAAAEKLCLSEFVETWARQLKLQRIHESALKEGFQRQVLQRGEPAQRTGSPRPHWLLRRCLASPHLEGVGFLLSLL
>NZ_CP019636.1|WP_087542105.1|5184112_5184352_-|hypothetical-protein
MRTDFDFPKKELLGPVVFRPDFNSFESININQAWSLFFTAGQEDKALGPNAELGKFLTYLLIAIALAGSLWTTVFSNLA

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Crispr_ID: NZ_CP019636_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_18

6035546-6035626

Orphan

Consensus_repeat	Method
ACTAACGCACCCTTGAAACCTTCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_18

>merge|NZ_CP019636|18|6035546-6035626|CRISPRCasFinder
ACTAACGCACCCTTGAAACCTTCTGAATTTCTACGCTAACCGACCACATTCGGATAGACTAACGCACCCTTAAAACCTTCT

>NZ_CP019636|18|17|6035546-6035626|CRISPRCasFinder
ACTAACGCACCCTTGAAACCTTCT	GAATTTCTACGCTAACCGACCACATTCGGATAG
ACTAACGCACCCTTAAAACCTTCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087546360.1\|6030068_6032498_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP019636.1\|WP_087542741.1\|6042129_6044007_+\|DNA-directed-RNA-polymerase-subunit-gamma	unknown	unknown	gnl\|CDD\|235055
NZ_CP019636.1\|WP_157679652.1\|6019868_6020186_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542734.1\|6026178_6028557_-\|cellulose-biosynthesis-cyclic-di-GMP-binding-regulatory-protein-BcsB	unknown	unknown	gnl\|CDD\|377001
NZ_CP019636.1\|WP_087542731.1\|6021506_6022565_+\|low-specificity-L-threonine-aldolase	unknown	unknown	gnl\|CDD\|224919
NZ_CP019636.1\|WP_087542744.1\|6051497_6052799_+\|histidinol-dehydrogenase	unknown	unknown	gnl\|CDD\|376389
NZ_CP019636.1\|WP_087542746.1\|6053701_6054529_-\|type-I-methionyl-aminopeptidase	unknown	unknown	gnl\|CDD\|237252
NZ_CP019636.1\|WP_157679727.1\|6053472_6053604_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|99749
NZ_CP019636.1\|WP_087542735.1\|6028725_6029991_-\|glycosyl-hydrolase	unknown	unknown	gnl\|CDD\|236844
NZ_CP019636.1\|WP_087542740.1\|6038369_6041669_+\|DNA-directed-RNA-polymerase-subunit-beta	unknown	unknown	gnl\|CDD\|234749
NZ_CP019636.1\|WP_087542733.1\|6023311_6025909_-\|UDP-forming-cellulose-synthase-catalytic-subunit	unknown	unknown	gnl\|CDD\|274400
NZ_CP019636.1\|WP_087542743.1\|6048349_6049987_-\|cellulase-family-glycosylhydrolase	unknown	unknown	gnl\|CDD\|365907
NZ_CP019636.1\|WP_087542730.1\|6020573_6021119_-\|GIY-YIG-nuclease-family-protein	unknown	unknown	gnl\|CDD\|198397
NZ_CP019636.1\|WP_087542728.1\|6018883_6019078_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087542738.1\|6036320_6036623_+\|30S-ribosomal-protein-S20	unknown	unknown	gnl\|CDD\|214366
NZ_CP019636.1\|WP_087542742.1\|6044187_6048264_+\|DNA-directed-RNA-polymerase-subunit-beta''	unknown	unknown	gnl\|CDD\|235052
NZ_CP019636.1\|WP_087542732.1\|6022585_6023218_-\|Vat-family-streptogramin-A-O-acetyltransferase	unknown	unknown	gnl\|CDD\|100040
NZ_CP019636.1\|WP_087542745.1\|6052975_6053407_+\|universal-stress-protein	unknown	unknown	gnl\|CDD\|366180
NZ_CP019636.1\|WP_087542739.1\|6036801_6037587_+\|TatD-family-hydrolase	unknown	unknown	gnl\|CDD\|223162
NZ_CP019636.1\|WP_087542736.1\|6032569_6034615_-\|porin	unknown	unknown	gnl\|CDD\|335962

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087546360.1\|6030068_6032498_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	4.97508e-13
NZ_CP019636.1\|WP_087542741.1\|6042129_6044007_+\|DNA-directed-RNA-polymerase-subunit-gamma	gnl\|CDD\|235055	PRK02625, rpoC1, DNA-directed RNA polymerase subunit gamma; Provisional.	0
NZ_CP019636.1\|WP_087542743.1\|6048349_6049987_-\|cellulase-family-glycosylhydrolase	gnl\|CDD\|365907	pfam00150, Cellulase, Cellulase (glycosyl hydrolase family 5).	1.50275e-45
NZ_CP019636.1\|WP_087542734.1\|6026178_6028557_-\|cellulose-biosynthesis-cyclic-di-GMP-binding-regulatory-protein-BcsB	gnl\|CDD\|377001	pfam03170, BcsB, Bacterial cellulose synthase subunit. This family includes bacterial proteins involved in cellulose synthesis. Cellulose synthesis has been identified in several bacteria. In Agrobacterium tumefaciens, for instance, cellulose has a pathogenic role: it allows the bacteria to bind tightly to their host plant cells. While several enzymatic steps are involved in cellulose synthesis, potentially the only step unique to this pathway is that catalyzed by cellulose synthase. This enzyme is a multi subunit complex. This family encodes a subunit that is thought to bind the positive effector cyclic di-GMP. This subunit is found in several different bacterial cellulose synthase enzymes. The first recognized sequence for this subunit is BcsB. In the AcsII cellulose synthase, this subunit and the subunit corresponding to BcsA are found in the same protein. Indeed, this alignment only includes the C-terminal half of the AcsAII synthase, which corresponds to BcsB.	7.29558e-105
NZ_CP019636.1\|WP_087542731.1\|6021506_6022565_+\|low-specificity-L-threonine-aldolase	gnl\|CDD\|224919	COG2008, GLY1, Threonine aldolase [Amino acid transport and metabolism].	2.99883e-129
NZ_CP019636.1\|WP_087542744.1\|6051497_6052799_+\|histidinol-dehydrogenase	gnl\|CDD\|376389	pfam00815, Histidinol_dh, Histidinol dehydrogenase.	0
NZ_CP019636.1\|WP_157679727.1\|6053472_6053604_+\|hypothetical-protein	gnl\|CDD\|99749	cd06260, DUF820, Domain of unknown function (DUF820). This family consists of hypothetical proteins that are greatly expanded in cyanobacteria. The proteins are found sporadically in other bacteria. They have been predicted to belong to the PD-(D/E)xK superfamily of nucleases.	0.000639265
NZ_CP019636.1\|WP_087542735.1\|6028725_6029991_-\|glycosyl-hydrolase	gnl\|CDD\|236844	PRK11097, PRK11097, cellulase.	6.96154e-49
NZ_CP019636.1\|WP_087542740.1\|6038369_6041669_+\|DNA-directed-RNA-polymerase-subunit-beta	gnl\|CDD\|234749	PRK00405, rpoB, DNA-directed RNA polymerase subunit beta; Reviewed.	0
NZ_CP019636.1\|WP_087542733.1\|6023311_6025909_-\|UDP-forming-cellulose-synthase-catalytic-subunit	gnl\|CDD\|274400	TIGR03030, Cellulose_synthase_UDP-forming, cellulose synthase catalytic subunit (UDP-forming). Cellulose synthase catalyzes the beta-1,4 polymerization of glucose residues in the formation of cellulose. In bacteria, the substrate is UDP-glucose. The synthase consists of two subunits (or domains in the frequent cases where it is encoded as a single polypeptide), the catalytic domain modelled here and the regulatory domain (pfam03170). The regulatory domain binds the allosteric activator cyclic di-GMP. The protein is membrane-associated and probably assembles into multimers such that the individual cellulose strands can self-assemble into multi-strand fibrils.	0
NZ_CP019636.1\|WP_087542746.1\|6053701_6054529_-\|type-I-methionyl-aminopeptidase	gnl\|CDD\|237252	PRK12896, PRK12896, methionine aminopeptidase; Reviewed.	1.18013e-177
NZ_CP019636.1\|WP_087542730.1\|6020573_6021119_-\|GIY-YIG-nuclease-family-protein	gnl\|CDD\|198397	cd10450, GIY-YIG_AtGrxS16_like, GIY-YIG domain found in CAXIP1-like proteins, iron-sulfur cluster assembly proteins, and similar proteins. The family includes CAX-interacting protein-1 (CXIP1)-like proteins and iron-sulfur cluster assembly proteins, both of which contain a GIY-YIG domain that shows statistically significant similarity to the N-terminal catalytic domains of GIY-YIG family of intron-encoded homing endonuclease I-TevI and catalytic GIY-YIG domain of nucleotide excision repair endonuclease UvrC. CAXIP1 is a novel PICOT (protein kinase C-interacting cousin of thioredoxin) domain-containing Arabidopsis protein that activates H+/Ca2+ exchanger CAX1, and its homolog CAX4, but not CAX2 or CAX3. Iron-sulfur cluster assembly proteins in this family also contain a C-terminal NifU-like domain that corresponds to a common region between the NifU protein from nitrogen-fixing bacteria and rhodobacterial species. The biochemical function of NifU is unknown.	5.67067e-34
NZ_CP019636.1\|WP_087542738.1\|6036320_6036623_+\|30S-ribosomal-protein-S20	gnl\|CDD\|214366	CHL00102, rps20, ribosomal protein S20.	6.02164e-29
NZ_CP019636.1\|WP_087542742.1\|6044187_6048264_+\|DNA-directed-RNA-polymerase-subunit-beta''	gnl\|CDD\|235052	PRK02597, rpoC2, DNA-directed RNA polymerase subunit beta'; Provisional.	0
NZ_CP019636.1\|WP_087542732.1\|6022585_6023218_-\|Vat-family-streptogramin-A-O-acetyltransferase	gnl\|CDD\|100040	cd03349, LbH_XAT, Xenobiotic acyltransferase (XAT): The XAT class of hexapeptide acyltransferases is composed of a large number of microbial enzymes that catalyze the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. Members of this class of enzymes include Enterococcus faecium streptogramin A acetyltransferase and Pseudomonas aeruginosa chloramphenicol acetyltransferase. They contain repeated copies of a six-residue hexapeptide repeat sequence motif (X-[STAV]-X-[LIV]-[GAED]-X) and adopt a left-handed parallel beta helix (LbH) structure. The active enzyme is a trimer with CoA and substrate binding sites at the interface of two separate LbH subunits. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients.	2.57742e-74
NZ_CP019636.1\|WP_087542745.1\|6052975_6053407_+\|universal-stress-protein	gnl\|CDD\|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	9.94291e-29
NZ_CP019636.1\|WP_087542739.1\|6036801_6037587_+\|TatD-family-hydrolase	gnl\|CDD\|223162	COG0084, TatD, Mg-dependent DNase [DNA replication, recombination, and repair].	4.11158e-118
NZ_CP019636.1\|WP_087542736.1\|6032569_6034615_-\|porin	gnl\|CDD\|335962	pfam04966, OprB, Carbohydrate-selective porin, OprB family.	6.3658e-09

>NZ_CP019636.1|WP_087542736.1|6032569_6034615_-|porin
MKPTVLDCYKFTMPKQWNRAYFLLHTVSISIFWILAVTDACLAQQNPHNQQLTDLQSGELLLVPQSPRSSKRQKSRSPSQTAPPLPRTLRQVTSVAVAPRAKPSSESNSYPADDIKQLESGFIQQQMPKKIPKDRPNSVPPRPTVTAQQAQNQIRQVSSNEKPTNIQAAPLPPPPSTPVTQEFTAPAAPTFNQVLNTQPQQAPLPPLPGTPTPTLNQPLNSSISNPSASTSNQLFNCQVVSSQPVPGTSAPTFNQLLNCQAATQSSVPNISASTSNQLLNCQVVPSPSAFGTSTSTTNQLLNCQVAQTTQTAQRQDLPTTPATPPTTPTAPSATPSTTSQLPNRNSSLIRSTALKEPSLQVQGVYITQGDDSAARARLSGIYPLTPQLLFGATLDLVSGENLLVDSRGDGLNINELFLATSIGGLPNLRFVLGQIDLTSYFDRNSFAKDGASQFFNPVFQTNPALSATGIASRPGLLVNWSVTDNIEAKAAVFSSSNKISDFALDGFAGELAIRYGNAIIRGTYASDRDAGIRDTFPESFGIARNTARTLFGPQKDDREEAYGLNAEVFIPNLKLGLFGRYGRYENRDLGEGADTYSFGLSFLDLFTPDDRLGLAYGRALSNDSLRRGDTPDVLEIYYDFQFLPNLRLGFTLQGRDGFEETVLGVRVRSEFNVTPRGRGSQ
>NZ_CP019636.1|WP_087546360.1|6030068_6032498_-|tetratricopeptide-repeat-protein
MFATDNPTRPIGHPPLTKGRVGEGFNRCVAFFFQIGITTKNSSSLFLITVSFLLLTHVVNLPLLQNNIAPAQAQKSSSAVQQGFNLLKKGWVNDAIKAFGQALKQNPQSLQAKLGLAISYNRAGRITEAWNTYQQVLAQDPSNQGALKIVGIMGTYRPEWQAQGIEALSTLLKLNPNDVQARSYRALLYTYQGKLSESLTDYQIVLANNPTPEAILGAAQAYSYSRNYQTALELFNRYRATGKPITGFAAIAYSSSLRETGNPKAAVQVLEGQLQRSNKLDRLGIETRAELAKAYVANQQSAKALAVLKPIQNRPDAILPLARSLNEIRTSTNNPAITQQVATLYRQAVANTPNPSPALLREAADVFTGLPQGEQIALQFYRQAASQLPNDKSLVVRQLALENKLGLLAKNELKKRLVAELGPLPTDPVQLQQIALALADIDTPDPELLSVYQTISPKVNVPFLNFRVAQIYLQLNDTNGARQALAAYTATPEGTRSLAPQLLAAEIERREGNLEASAQRFQAVLVTNSGSDDVVDGALRGLAGARIQQRRFDEALAAYDQLIVRQPQNLTTQLGRTSIAYQAKKISEQEAQAVLNNWLATQPATNAPPELFSLVGVLPAEPQREPLYNYLAQIDPSYLPVQLRLVQVIAKRNPTQAQARVKQLIARLPNNANTYQLQGELARAIGDLDLAGKAYENILAQQPDNIDALAALGGIRFEQQRFESAQQIYSQVVAQKPQDKDARRALAGLSAIADQPLTALTQLEQLELEQISQGASDIEVSRQRQQIQEDFLQRRGFQPPWENYERRGK
>NZ_CP019636.1|WP_087542735.1|6028725_6029991_-|glycosyl-hydrolase
MQYLPRLAVIVSMIVLTSCNLGYSVINTEASDARNPVLTATPLSGSESPSVFLAALPQSIPNRELLAQSWESYRRRFIQGDGRVIDYEAGDRSTSEGQAYAMLRAVLIDDSATFALTLNWGENNLQRQANGKRTDNLWAWKWGRNADGNWGTIDSNFASDGDIDTITALILASRRWNRPEYLNLAKAKLQDLWNLSVVVGHEGKFYLLPGPAAAFIPNASTLYLNPSYLAPYAFRLFAQVDQQHDWLSLVDSSYEVLEKSASLSTVGLPSDWVALDTKTGKYQPLPQSSPLQTLYGFDAYRVWWRLSLDLAWFNSPQARRYLQTHSQYLQKLWRERSRLPASIDLTGKGLVDYEATAQHAMLYAAWGLVEPRIAQELLVKKLLPQYKQGIWDDKSAYYTQNLAWLGLFSPSGLPQQLLKGK
>NZ_CP019636.1|WP_087542734.1|6026178_6028557_-|cellulose-biosynthesis-cyclic-di-GMP-binding-regulatory-protein-BcsB
MKLLFHLSQISTKAIIFTLCLLLFPGSLISAQAQSEEELQPQDSHKSRESQQQSILLAQAIKPKADREDKEDTKEVANAKNLITYNLEFNRSPIVGNRLRLRGIHGEGRLGFNRPRGWKIAQVQALIRFQHSPSLYAKRSNLTVLVNDTAVGSVSLNLKQSQLGQVLININPKLLQDYNEIKFVAQQNSSQECTDPQDPELWTEILPDSKLIFGFQRQPNPLNFSRYPYPFFDQLGLETNHIVYLQPSQTSQYWLTAAARLHAAFGRLADFRPVQTSLVSDIKGVKPEQRLVIIGTPTEQPVLSSLKLPVSVVGREILDINQKAVPEDTGVLIATTTKKEGGTPVLIATGNGSKGVAKAVQFLVQPDLRKMGTGSVVFVNQVSEAATPDPRQWPRYIPEENTFRLSDLRTPLNGEPFSDVTVRGSAAPPVEIDFHALPDDRFMRGSTMNLVYSYGPQMNPRTSALEVLLDGRYIGGARLTSDSGETRQTLRVDLPAHLLRSNSLIQIFFRMNPKEPFNRQQCISAADQQLIGTLHTETSFDLKRETSVQIPDLGLLQFGFPFAAPQDLSRTAIVLPQNPSRTDILTLLAFSERLGRITQADSVKFQVYTPESVPDSVRKNEHLVGIGTREKFPFPEVFKSGGLNLSQAFSRVSAQGTIQTPQDSQGMIKQIISPWSQERVILALTAQTETGLERVQQVIDQDPLFFQLKQDTVLIGSDKNNPSPYNVDDYQLEFFRSTPSKTRVENTNLLSKILRFLQENWLLLPVGILGVSLLLYGIVQLYLKRLAVTDRN
>NZ_CP019636.1|WP_087542733.1|6023311_6025909_-|UDP-forming-cellulose-synthase-catalytic-subunit
MSSSLNSRQRRRFILTRWLIDITPQFFDRALEKVGVKQFKWLVLLLLILSVPLIITPIRVWQQAVIALFLVILGQLIMQAEEQESSTEISQYYHLFMVWLSLVTTLRYFYYRTSYTLNFDGLVNSIACLLLYAAELYAVLTLALAYFQTLRINERQPVNLSTIPQQEWFKVDIYIPTFNEDVEIVRKTALAAMACDYAPGKKIVYVLDDGRPERYKENDPRREKFRQRREQIRQMCEEIGCIHMTRDNNNHAKAGNINNAFHKTDGELVLILDCDHIPSRQFLMHTVGFFFDQKVSFVQTPHWFYNPDPFERNLLTGGKIPAGNELFYKVLQKGNDFWNAAFFCGSAAIIRKSHALEVEGVAVETVTEDCHTALRLHSRGYKSVYYDKIMVAGLAPDTFSSYVGQQVRWARGMAQILRVENPLFNPKLKLTIPQRICYFSATSHFLYGYPRLIYAIVPTLFLLFGINPIRGLGLETLSYAVPHILLALFTNHIIYKTVRFSFWNEIFEFVMAFQAGWVTMLALINPKLGSFNVTDKGVNVTKRTFDWQSMRGLIIVTAFVFASLFAVPYWLLLRPEDWQAVLVNTLWSGFNLILLIAALLVGFEQPQVRSAHRLQRRLPVVISSSNQTFRGETINISETGALISLESWPNLPDEIDVEIMGDFTARASLTAQVVRVSPVSDTETLLAIDFVNPSRAQMDDLILILYSDVREWYSQKRQSIDQPIASLKFLATSLNRSLRDIKPITRHQVRKRVNAVGELYWDGHFFPGITTELGVTGLRLEILSKKARSGDRLLGQEDLHKMRNLKPLVGLLLSREEGNPSPSKFIAEISTVKEETNGKIVIDLNFPTEFKQRQGTKIKQLLQVL
>NZ_CP019636.1|WP_087542732.1|6022585_6023218_-|Vat-family-streptogramin-A-O-acetyltransferase
MQYPDARVPHPMQGFPQVCFIKNVVSNPNIIIGDYTYYDDPEDSENFERNVLYHYPFLGDKLIIGRFCALATGVKFIMNGAFHKMSGFSTYPFEIFGNGWERVMPNKGEYPFKGDTVIGNDVWIGYEALIMPGVKIGDGAIVAAKSVVVKDVPPYTVVGGNPASVLRQRFPDETINLLLEIAWWNWDIEKITRNLEKIVGADIEALNKCV
>NZ_CP019636.1|WP_087542731.1|6021506_6022565_+|low-specificity-L-threonine-aldolase
MNFCSDNVVGVSPEIMAALLAASHGVSMPYGNDDCTQRLNFLFSELFETEVVVFPVATGTAANALALSVMTPPFGAIYCHHQSHIHSDECGAPEFFTGGAKLVTLPGEHGKIDAIDLATALARAGTGVVHHVQPATVSLSQVTEAGTVYSIDEVSQIAEVAHAHQLNLHMDGARFANAVVSLGCTPADVTWRAGVDVLSFGATKNGAMAAEAVVFFNRDLANTFRYRLKRSGHLFSKMQFLSVQLEAYIKNDLWRKNATHANQMAKQLAQKLTILPGVTLCHPVEANEIFIQMPEQVIINLIADGFKFYRWDGEDSTTVRLITAFNTQEEDVRAFSEAAKAHCTRHLSLSIS
>NZ_CP019636.1|WP_087542730.1|6020573_6021119_-|GIY-YIG-nuclease-family-protein
MTTETNIASLASLEYIPYINDNGQLPEQLQGEIGVYAIFDQEKILHFVGYSRDVYLSLKQHLVRQPQHCYWVKAQTIERPNRTVLENIEHTWIAENGSVPAGNAQNKDKWTQPINVKVLMTREEQTNYDNPTNDEIAQTKIIKNVARRVEAEIIAILEVRGLQTQIRFNPKLKENGLLDLK
>NZ_CP019636.1|WP_157679652.1|6019868_6020186_-|hypothetical-protein
MSKRIQIIGEHRVSMTDERGSGRFCREILTSANQFFSKKLSTWNCLFAIKGSINSSNLQISFPQLIAEQVPSLNDLLSKQAGTVLSTWQSIRQNLVGIPALFAVI
>NZ_CP019636.1|WP_087542728.1|6018883_6019078_-|hypothetical-protein
MLNRQTKTYRTVLAPWAVVRWVSPTERIVIGRFRSRSDADGHLAVLQRLTPEADLRVIVDMEQD
>NZ_CP019636.1|WP_087542738.1|6036320_6036623_+|30S-ribosomal-protein-S20
MANTKSALKRAKIAERNRLRNKSYKSAVKTLMKKYFTAVETYAANPSPESKQEVLARMSEAYSKIDRAVKRGILHPNNGARKKSKLAQRLKAHSQPAATA
>NZ_CP019636.1|WP_087542739.1|6036801_6037587_+|TatD-family-hydrolase
MQLIDTHVHINFDVFQPDLEAVRSRWQQAGVVHLVHSCVEPAEFSSIQALAHRFPEISFAVGLHPLDTQKWDENTAQEIVSLAGSDSKVVAIGETGLDFYKADNYEQQRKAFETQLAIATELEKPVIIHCRDAAAVVREVLQKWKKLKGESVRGVMHCWTGSPEETQWFVDLGFYISFSGTVTFKNAKQIQESAAIVRSERLLIETDCPFLAPVPKRGERRNEPAYVRYVAEQVARVRGETVEAIAAVTTQNACDLFGLAV
>NZ_CP019636.1|WP_087542740.1|6038369_6041669_+|DNA-directed-RNA-polymerase-subunit-beta
MTNETIMEPAFLLPDLIEIQRSSFRWFLEEGLIEELNSFSPITDYTGKLELHFLGQNYRLKEPKYSVEEAKRRDSTYAVQMYVPTRLINKETGEIKEQEVFIGDLPLMTDRGTFIINGAERVIVNQIVRSPGVYYKSEIDKNGRRTYSASLIPNRGAWLKFETDRNDLVWVRIDKTRKLSAQVLLKALGLSDNEIFDALRHPEYFQKTIEKEGQFSEEEALMELYRKLRPGEPPTVLGGQQLLDSRFFDPKRYDLGRVGRYKLNKKLRLQVPEPVRVLTPQDILAAVDYLINLEYDIGSTDDIDHLGNRRVRSVGELLQNQVRVGLNRLERIIRERMTVSDAEVLTPASLVNPKPLVAAIKEFFGSSQLSQFMDQTNPLAELTHKRRLSALGPGGLTRERAGFAVRDIHPSHYGRICPVETPEGPNAGLIGSLATHARVNQYGFLETPYRPVENGRVRFDLPPVYMTADEEDDLRVAAGDLPIDENGNIIGPQVTVRYRQEFSSTTPEQVDYVAVSPVQIVSVATSMIPFLEHDDANRALMGSNMQRQAVPLLKPERPLVGTGLEAQAARDSGMVIVSRTDGEVTYVDATEIRVRPKPNAPEIKYPISKYHRSNQDTCLNQKPLVYIGERVVAGQVLADGSSTEGGELALGQNIVVAYMPWEGYNYEDAILISERLVQDDIYTSIHIEKYEIEARQTKLGPEEITREIPNVGEDALRQLDEQGIIRIGAWVESGDILVGKVTPKGESDQPPEEKLLRAIFGEKARDVRDNSLRVPNGEKGRVVDVRLFTREQGDELPPGANMVVRVYVAQKRKIQVGDKMAGRHGNKGIISKILPFEDMPYLPDGSTVDIVLNPLGVPSRMNVGQVFECLLGWAGHTLGVRFKLTPFDEMYGEESSRSIVHGKLQEARDETGKNWVYNPDDPGKILVYDGRTGEPFDRPVTVGVAYMLKLVHLVDDKIHARSTGPYSLVTQQPLGGKAQQGGQRFGEMEVWALEAFGAAYTLQELLTVKSDDMQGRNEALNAIVKGKAIPRPGTPESFKVLMRELQSLGLDIAVHKVETQADGSSLDVEVDLMADQGNRRTPPRPTYESLSRESLEEEE
>NZ_CP019636.1|WP_087542741.1|6042129_6044007_+|DNA-directed-RNA-polymerase-subunit-gamma
MRAAQNNQFDYVKIGLASPERIRIWGERTLPNGQVVGEVTKPETINYRTLKPEMDGLFCERIFGPAKDWECHCGKYKRVRHRGIVCERCGVEVTESRVRRHRMGYIKLAAPVAHVWYLKGIPSYISILLDMPLRDVEQIVYFNSYVVLSPGNAETLTYKQLLSEDQWLEIEDQIYSEDSTLQGVEVGIGAEALLRLLADINLEQEAESLREEITNAKGQKRAKLIKRLRVIDNFIATGSKPEWMVMTVIPVIPPDLRPMVQLDGGRFATSDLNDLYRRVINRNNRLARLQEILAPEIIVRNEKRMLQEAVDALIDNGRRGRTVVGANNRPLKSLSDIIEGKQGRFRQNLLGKRVDYSGRSVIVVGPKLNIHQCGLPREMAIELFQPFVINRLIRSGMVNNIKAAKKLISRSDPSVWDVLEEVIEGHPVLLNRAPTLHRLGIQAFEPILVEGRAIQLHPLVCPAFNADFDGDQMAVHVPLSLESQAEARLLMLASNNILSPATGRPIITPSQDMVLGAYYLTAENPHATKGAGRYFASLDDVVMAYEQQQIDLHAYIYVRFDGEVESGEPDTEPVEVIPNDDGSRTLMYKFRRIREDAQGNLVSQYIRTTPGRVIYNKAIQEALAS
>NZ_CP019636.1|WP_087542742.1|6044187_6048264_+|DNA-directed-RNA-polymerase-subunit-beta''
MNNNKMIFRNRIVDKGQLRNLISWAFTHYGTARTAVMADKLKDLGFRYATKAGVSISVDDLMVPPSKRSLLEAAEAEIRATEERYQRGEITEVERFQKVIDTWNGTSEALKDEVVNHFKRTNPLNSVYMMAFSGARGNISQVRQLVGMRGLMADPQGEIIDQPIKTNFREGLTVTEYIISSYGARKGLVDTALRTADSGYLTRRLVDVSQDVIIREFDCGTTRGIPLRSMTEGEKVLINLGTRLLGRVIAEDVVHPKTGEVIAARNTPVSDDLAKHIEKSGVQEVVVRSPLTCEAARSVCQHCYGWSLAHAKMVDLGEAVGIIAAQSIGEPGTQLTMRTFHTGGVFSGEVAKQVRAKSDGTIRIPRKLRTRPYRTRHGEDAQYVEANGNIILEVITDNSDSPTNQEIAVTQGSTLYVVDGQKIKTGQLLAEVAIGGRTTRVNTEKAVKDVASDMAGEVKFADVIAEQKTDRQGNTTTTAARGGLIWILSGEVYNLPPGAELVVKNGDTIDSNGVLAETKLTTLHGGVVRLPEATPGKGTREIEIITASVVLDQATVTAQTAQGRNNYLVTTGNNQVFNLRATPGTKVQNGQVVAELIDDRYRTTTGGLLKYAGVDVQKKGKAKQGYEVVQGGTLLWIPEETHEVNKDISLLMVEDGQFVEAGTEVVKDIFSQNSGVIEVTQKNDILREVVIKPGELLMVDDPEAVMGKDGTFIQPGEELLGQVATELRYIEYVESPEGPALLSRPVVEFAVPNNPDVPSTTSVSQQTGRSIQLRAVQRLPYKDSERVKTVEGVELLRTQLVLEIEQEGEQDHNASPLAADIELVADADDPEIQRLQLVILESLVLRRDIAADATQGSTQTSLEVEDGQTIAPGAVIARTQILCKEGGIVRGVQKGTEAVRRCLVLRHTDMTTTNLSAPPKVKVGDLVVEGVEIAPGVFAEESGQVVAVQKGEGKKAQGEVTPSEESALTTQNYSVTLRVGRPYRVSAGAVLQVDDGDLVQRGDNLVLLVFERAKTGDIIQGLPRIEELLEARKPKEACILARRSGEVKVVYGDGDEAIAVKVIEPNGVVTDYPLGPGQNLIIPDGAHITAGQALTDGPSNPHEILEIFFNLGSEEGVYVCASHALQKVQTFLVNEVQSVYQSQGIDIADKHIEVIVRQMTSKVRVDDGGDTTMLPGELVELRQIEQVNEAMAITGGARAQYTPVLLGITKASLNTDSFISAASFQETTRVLTEAAIEGKSDWLRGLKENVIIGRLIPAGTGFNAYEEPGAIEDYAADMTSSVLDEVDDPLDMVLDDRTARSYQLDSPTLGDGFGTRRSPDKSILDEDDFILPSAGDSDIDDLVEDEYEDDEEDDDEDY
>NZ_CP019636.1|WP_087542743.1|6048349_6049987_-|cellulase-family-glycosylhydrolase
MKFYFYKKKQKKWKFYAQLFILSIVTIIFCLGIVANFPVRSQESVVTTGTTLELSLSTNGAKIIDAKGQQILLRGVNWFGMETETHVPHGLWKRDYKELVAQIGSLGYNLIRLPYSVEALRSDNISGIDFSIGSNKELEGKTSIEVMDIIIQEAERQGLLVLLDSHRLSDKRISQLWYEDGFTEADWIDTWKMLAERYKNQTNVIGADLKNEPHGKASWGTNDLATDWRLAAERAGNAILEINPNWLIVVEGVEKNVPEQKLPKHWQGGNLEGVKRYPVRLSRRNKLVYSPHEYGPGVAEQPWFADPKFPKNLINRWQIGFHYISSQNIAPILIGEFGGRQVDTSSKEGIWQNKFVRYIKQKKLSFAYWSWNPNSADTGGILLDNWQTVDIPKQQLLSQLLPVTFSQVAPVQNSAGVGEVFSSPSPLSPSSPSSSPSPPFRISSAQLTVTSDIYTNWQTGFCVSFKIMNHGSRRVDNWQLMFNMKQAAINNSWNGNFKPQGATQYIVTPLDWGQMIEPNQVRDLGFCANKLGSDYQPKQIEIKRK
>NZ_CP019636.1|WP_087542744.1|6051497_6052799_+|histidinol-dehydrogenase
MLRIITQQADVRAELQRICDRTHDEQVLHKEATVREVLQAVKRQGDKAVLHYTAEFDKQTLKPEELRVTGSELDAAYQQVSKELLQAIRLACRQIEEFHRQRVPKSWVQFGDNDVVLGKRYTPVDRAGLYVPGGRAAYPSTVLMNSIPAKVAGVPRVVMVTPPGADKTMNPAVLVAAQEAGVQEIYRVGGSQAIAALAYGTETIPKVDVITGPGNIYVTLAKKLVYGTVGIDSLAGPSEVLIIADETANPVHVAADLLAQAEHDPMAAAILLTTDTALAKNVQVAVERQLVDHPRRLLTEKAIAHYGLIVIVESLQAATELSNEFAPEHLELEVEDPWELLPMIRNAGAIFLGHSTPEAVGDYLAGPNHTLPTSGAARYASALGVETFMKHSSIIQYSQTALEKVAGAIDVLATAEGLPSHTDSVRRRVQKEE
>NZ_CP019636.1|WP_087542745.1|6052975_6053407_+|universal-stress-protein
MTSVLKTILVALDESELADRVIQTLQELVLPKDSKVILCHVFPAPESEMELPADRPHSESPTFSYLQIEKQLQSYQTLLPVETDIELVTGDPAEEIIRLANIYKAELIMIGSRGLTGMKRIVQGSVSSQVVEEANCSVLVVKP
>NZ_CP019636.1|WP_157679727.1|6053472_6053604_+|hypothetical-protein
MDNNYYFVDGELVLMTEPTRLHEEIINFLLDEFKAKINGLQLN
>NZ_CP019636.1|WP_087542746.1|6053701_6054529_-|type-I-methionyl-aminopeptidase
MNILSNLLSQPAQSNSQKRQRRGIEIKSPREIEIMRQSAKIVATVLKEISELVKPGMTTADLDAHAEKRIREMGATPSFKGYHGFPGSICSSINNEVVHGIPSAKKVIRTGDVLKVDTGAYYQGFHGDSCITIAVGEVTPEAARLIRVAEEALFKGIEQVKAGNYLLDIAGAVEDHVKANGFNVVEDFTGHGVGRNLHEEPSVFNFRTREMPNVKLRAGMTLAIEPILNAGSKYTRTLSDRWTAVTVDSSLSAQFEHTVLVTETGYEILTDRSKV

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Crispr_ID: NZ_CP019636_19

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_19

6281907-6282066

TypeV-U4

Consensus_repeat	Method
CAAACGAATAAAGAAGAACAAACATCAC	CRISPRCasFinder

2 spacers

c2c9_V-U4

The CRISPR arrays of NZ_CP019636_19

>merge|NZ_CP019636|19|6281907-6282066|CRISPRCasFinder
CAAGCTAGTCAAGAACGACAAACATCAAAACAGCAGGTGATTTTGAGACAAACAACCTCTGCACCGCAAACGAATAAAGAAGAACAAACATCACGGCAACAGGTCGTTGTCAGGCAGTCTGCGTCTTCTTTACAAACGAATAAAGAAGAACAAACATCAC

>NZ_CP019636|19|18|6281907-6282066|CRISPRCasFinder
CAAGCTAGTCAAGAACGACAAACATCAA	AACAGCAGGTGATTTTGAGACAAACAACCTCTGCACCG
CAAACGAATAAAGAAGAACAAACATCAC	GGCAACAGGTCGTTGTCAGGCAGTCTGCGTCTTCTTTA
CAAACGAATAAAGAAGAACAAACATCAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087543086.1\|6279452_6280148_-\|lipase	unknown	unknown	gnl\|CDD\|224001
NZ_CP019636.1\|WP_087543112.1\|6288986_6289823_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP019636.1\|WP_087543082.1\|6276752_6278675_+\|sodium:proton-antiporter	unknown	unknown	gnl\|CDD\|223104
NZ_CP019636.1\|WP_087543090.1\|6282384_6282738_-\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|184253
NZ_CP019636.1\|WP_087543104.1\|6286364_6286784_-\|plastocyanin	unknown	unknown	gnl\|CDD\|235060
NZ_CP019636.1\|WP_017315076.1\|6272440_6272776_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543101.1\|6284681_6285836_-\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	c2c9_V-U4	-	gnl\|CDD\|223747
NZ_CP019636.1\|WP_087543078.1\|6275588_6276176_+\|cyclase	unknown	unknown	gnl\|CDD\|176875
NZ_CP019636.1\|WP_087543073.1\|6271519_6272038_-\|HNH-endonuclease	unknown	unknown	gnl\|CDD\|224321
NZ_CP019636.1\|WP_087543084.1\|6278681_6279338_-\|cytochrome-bc-complex-cytochrome-b-subunit	unknown	unknown	gnl\|CDD\|224209
NZ_CP019636.1\|WP_087546380.1\|6289819_6290719_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP019636.1\|WP_087543109.1\|6287980_6288196_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|372949
NZ_CP019636.1\|WP_087543092.1\|6282961_6283399_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP019636.1\|WP_087546379.1\|6269394_6270792_+\|TldD/PmbA-family-protein	unknown	unknown	gnl\|CDD\|223389
NZ_CP019636.1\|WP_087546381.1\|6291247_6291982_-\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379312
NZ_CP019636.1\|WP_157679659.1\|6270803_6271079_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543095.1\|6283511_6284489_+\|EamA-family-transporter	unknown	unknown	gnl\|CDD\|273359
NZ_CP019636.1\|WP_087543106.1\|6287366_6287858_-\|cytochrome-c-550	unknown	unknown	gnl\|CDD\|184185
NZ_CP019636.1\|WP_087543071.1\|6271086_6271503_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543076.1\|6272120_6272369_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087543086.1\|6279452_6280148_-\|lipase	gnl\|CDD\|224001	COG1075, LipA, Predicted acetyltransferases and hydrolases with the alpha/beta hydrolase fold [General function prediction only].	2.15412e-27
NZ_CP019636.1\|WP_087543112.1\|6288986_6289823_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	1.49278e-92
NZ_CP019636.1\|WP_087543082.1\|6276752_6278675_+\|sodium:proton-antiporter	gnl\|CDD\|223104	COG0025, NhaP, NhaP-type Na+/H+ and K+/H+ antiporters [Inorganic ion transport and metabolism].	2.49966e-77
NZ_CP019636.1\|WP_087543090.1\|6282384_6282738_-\|c-type-cytochrome	gnl\|CDD\|184253	PRK13697, PRK13697, cytochrome c6; Provisional.	1.01346e-43
NZ_CP019636.1\|WP_087543104.1\|6286364_6286784_-\|plastocyanin	gnl\|CDD\|235060	PRK02710, PRK02710, plastocyanin; Provisional.	4.34177e-66
NZ_CP019636.1\|WP_087543109.1\|6287980_6288196_-\|hypothetical-protein	gnl\|CDD\|372949	pfam14177, YkyB, YkyB-like protein. The YkyB-like protein family includes the B. subtilis YkyB protein, which is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 150 amino acids in length. There are two conserved sequence motifs: NRHAKTA and HLG.	0.00139351
NZ_CP019636.1\|WP_087543101.1\|6284681_6285836_-\|IS200/IS605-family-element-transposase-accessory-protein-TnpB	gnl\|CDD\|223747	COG0675, COG0675, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	8.0388e-53
NZ_CP019636.1\|WP_087543078.1\|6275588_6276176_+\|cyclase	gnl\|CDD\|176875	cd08866, SRPBCC_11, 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.	1.81166e-58
NZ_CP019636.1\|WP_087543073.1\|6271519_6272038_-\|HNH-endonuclease	gnl\|CDD\|224321	COG1403, McrA, Restriction endonuclease [Defense mechanisms].	1.56207e-29
NZ_CP019636.1\|WP_087543084.1\|6278681_6279338_-\|cytochrome-bc-complex-cytochrome-b-subunit	gnl\|CDD\|224209	COG1290, QcrB, Cytochrome b subunit of the bc complex [Energy production and conversion].	3.99127e-41
NZ_CP019636.1\|WP_087546381.1\|6291247_6291982_-\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	3.27972e-14
NZ_CP019636.1\|WP_087546380.1\|6289819_6290719_-\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	8.44126e-85
NZ_CP019636.1\|WP_087546379.1\|6269394_6270792_+\|TldD/PmbA-family-protein	gnl\|CDD\|223389	COG0312, TldD, Predicted Zn-dependent proteases and their inactivated homologs [General function prediction only].	1.15956e-135
NZ_CP019636.1\|WP_087543092.1\|6282961_6283399_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	5.33208e-15
NZ_CP019636.1\|WP_087543095.1\|6283511_6284489_+\|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].	5.17727e-16
NZ_CP019636.1\|WP_087543106.1\|6287366_6287858_-\|cytochrome-c-550	gnl\|CDD\|184185	PRK13618, psbV, cytochrome c-550; Provisional.	9.22315e-114

>NZ_CP019636.1|WP_087543086.1|6279452_6280148_-|lipase
MSLPTVILPGYLESAVAYLPLEQSLQELGFSTVMVPLRRRDWIPTLGGRPITPILRLLDDTVKQILQQSNASQVNLIGHSAGGWISRIYLGEKPYSGRGEVTSFAWKAHPLVATLITLGTPHASQERWTRWNLDFVNQNYPGAFYKNVRYVCVAGKTIFGQRRRGGWLAYSSYQLTCGKGNTWGDGITPIEAAHLEGAENIVLEGVRHSPRSSPMWYGSPGPLKDWVKYLV
>NZ_CP019636.1|WP_087543084.1|6278681_6279338_-|cytochrome-bc-complex-cytochrome-b-subunit
MHNTQSDVVLRRITTILSVVIVTLTLIGATTGILLSFYYEPAAGRAYQSLKIIDTEVSYGWLFHKAHQIAGNAAVVIALIQIVVMFVSRQFSKSWLAAWISGIFFTLSAIGLGWTAMILSWDQEGFWRFNIELGTIEAIPFVGSVLRDILTGGGAISTVTVQHLYTIHSYLISVAAIILAVVHLLSVLWQEKQIKKMYAEADVSETGNIPPKPANAQG
>NZ_CP019636.1|WP_087543082.1|6276752_6278675_+|sodium:proton-antiporter
MEASFEITLQMVITVFAGISAQVLAASLRVPSIVFLLMFGILLGSDGIGVLHPHVLGTGLEVIVALATAIILFEGGLNLDLQELGKVSTSLQLLVTLGTMSTLLGGSMAAHWLGEFPWTIAFLYASLVVVTGPTVVSPLLKQINVDRQVATLLEGEGVLIDPVGAILAVVVLNTILNDHTDFITAMSSLILRLGIGGVIGAAGGWLMSFISKRANFLSFELKNLVVLAGLWGLFAQSQMILSESGLMAVVVAGVVFGDSSVPEERLLRRFKGQLTILSVSVLFILLAADLSIASVFALGWGGVFTVLVLMFVVRPINILLCTWNSDLNWRQKLFLSWVAPRGIVSASVASLFAILLTQRGINGGEAIKALVFLTIIMTVVCQGLTAGWIAKCLQITSKDATGAVIVGCNPLSLLIARLFQEQGEQVVMIDTDQQRCELAEAQNLRVIASSALDTGVLEEAGLASMGTFLAMTSNGEVNFVLAQRAAEEFNPPRVLAVFPRDPQATTSTKENPVNQAFIPDLPIKTWNEYVNDGRVKLGTTTLNESDFDFQQTHMQALIKAGELIPLLVVREEHLQVMPATQEWEVGDRIIYLLHDPRPHLLKRLSGASQSTRLSLEKLPEVEEIPLAKLSQLSTSDAPTP
>NZ_CP019636.1|WP_087543078.1|6275588_6276176_+|cyclase
MTEEHNIQQELDLSALSNDTELEPDVVARGADVQAVKVQVEQIAERQRQITAQLQIPQPVERVWKVLTDYEALAEFVPNLTKSRLLEHPQGGIRLEQVGSGRFLRIDFCARVVLDLEEYFPKEINFRMVEGDFKDFSGTWLLDPYPLGENWGTRLCYTVKVWPKRTMPVGMIERRLSSDMQLNLLAIKQRVSEYF
>NZ_CP019636.1|WP_017315076.1|6272440_6272776_+|hypothetical-protein
MHTIARTPTTDMEVTSIRLERELKDKLKELAGNQGYQALIRDILWNYVQQKSGEWKPRFSRADIRASIAATAQQEERCVLTGQLIQPKQPMLLGLTRNGDMVPLSVESLAG
>NZ_CP019636.1|WP_087543076.1|6272120_6272369_-|hypothetical-protein
MKFSVKSVYPISTSSRVVNCRFSWKSAAMGVEYLFMGDGRWNKWQLTEGNHDSRYASIDVLNAVPKLKRRSGRYSQQDAVPI
>NZ_CP019636.1|WP_087543073.1|6271519_6272038_-|HNH-endonuclease
MTSAMQVLEQSVVVFSQNYLPLCRVNIKRAIVLLVTNKAEPLDFSTQSGWEVHSPSLVLYVPKHIRLTIASIERMWKVPVVNRREVLRRDHHSCQYCGSSKHLTLDHVIPRSRGGQHTWDNVVAACVRCNSRKGDRTPQEAGMPLRTKPKAPVHPTLFFAEQFWIDMQANLE
>NZ_CP019636.1|WP_087543071.1|6271086_6271503_-|hypothetical-protein
MLKLTYTETSFCLECLVQSLEEWVAQRVILALRVGQCLCVEPSTASFLLPVNLPGVEILKTLVNRHNSEIIALCGCDNECVEVTLRGYWLSNGSQDADGIFITAMSDLSYGDRSASRTEFFLYKLWQEAQQRASVMSE
>NZ_CP019636.1|WP_157679659.1|6270803_6271079_+|hypothetical-protein
MQESGSREHKLQEVRPQDRIGSSVGDWRWRWRWRSLSVRRSLSVRRSFSAGFTRTRVRLVTGEGVSLRTRDAPANMTNQGHLSAITHQVDS
>NZ_CP019636.1|WP_087546379.1|6269394_6270792_+|TldD/PmbA-family-protein
MQTLVADVQNLLSDLLKRYSSRVDYLMIRLEEAEGTDILLRGDKVETLSEGISIGGQIRACYKGGWGFSSFNQLSTISDRIEEAIAAAKIVGDEETILAPIDIVQAVCSLPLTGTDPRQIPLNKKKQLCDRYTELLKSVDSRITTTSVRYGDSAQRVILATSEGTFIEQSWVDMEMRFAATARNGETVQTGRETTGSRKAFEDLLALDEQVKDAAQRAVAALSLPSVKGNTYTVVIDPILTGLFVHEAFGHLSEADMAYENPDLLEVMTLGRRFGPKELQIFDGAAPQGHRGSYLYDDEGTPATTTQLIKDGVLIGRLHSRETAGKLNEAPTGNARCLNYHYPPVVRMTNTWIERGKTPVADLFSGIKEGVYARNWLGGMTNGEMFTFSAGEAWMIRNGKIAEPVKDVTLSGNVFQTLADIEAIGDDFYWDESGGCGKGGQNGLPVGCGGPSLRIRDVVVGGEVA
>NZ_CP019636.1|WP_087543090.1|6282384_6282738_-|c-type-cytochrome
MRIVVFVVFLAIALFQFTFTHTVFAAEISNGAKIFNDNCASCHIGGGNILIAEKTLKKEALSKYLERYDADSIQAIIYQVQNGKNAMPAYKSKLSEQEILEVAAYVFQKSEQGWQGS
>NZ_CP019636.1|WP_087543092.1|6282961_6283399_-|MarR-family-transcriptional-regulator
MTNLDSASNTAWRAFLTVHMKVIDLIEQELAQAELPSLEWYDVLFALKEAPECKLRLHELAQAVLLSRSNITRLVDRLEAVGLIRRERCSSDRRGAYAVLTEEGLAMQKRMWPVYAQGIAKYFACHLNEEEILVLTNVFKRMLAR
>NZ_CP019636.1|WP_087543095.1|6283511_6284489_+|EamA-family-transporter
MYGNFALVTSQLRVALEILAMQEFNKGTQHLVNWLGLTAVVSASTLWAIAANVANSLFSIGVNPLDLAGVSALIATLGLTLLNTLLGGGGTKAISKKQFALGILFALFVGADYIAIAKLPVAVAIVLIFNSPTIVVVWTAITTRHFPSAKVLLALVLSVIGVVLVSGMLARETEQFNAFGILVGLTTAVLFAIYTMWSEKVSVSGTSIEVMQQIFSVASLFWIAYLFTQGMPIQLLQGENFPKVLYMGIAGNLFPYLLYLWGIQRVQAQRAVIVATIEPVIAAVLAWVWFGQRLTAMQIIGGALILMAITALQLTKSQAQNSLQQ
>NZ_CP019636.1|WP_087543101.1|6284681_6285836_-|IS200/IS605-family-element-transposase-accessory-protein-TnpB
MKARYQYRFYPTDQQRLSLAQLFGCVRVVWNDALALSKVSKFPGYNSLAKSLTLSKKTEERKWLSDVSSVPLQQSLKQLEVAYKNYFDSLKGKRKGKKVGQPRFKKKTNSQSATFTKAAFSVQRGEVYLAKIGTIKPIWSRELSSEPSSVTVIKDCANRYFLSFVVEVQPNLAVTNNQSIGIDLGIKTFAVMSNGEKALSPNYSKHDRKIRRLQRKLARQQKDSKRRNGTRIRIAKLHNQISDTRKDFLQKLSTKIVKDNQVIVLEDLNVSGMVKNRRLSRVINLQGWREFRNLCEAKSEKFNRDFRVIDRWQPTSQICSCCGFRWGKIDLSVRSILCLNCSTEQQRDENASKNIEMVGMGHRHDLKCTQRDCKTTSVAEPNEA
>NZ_CP019636.1|WP_087543104.1|6286364_6286784_-|plastocyanin
MKFIASNLRRLGLALLTIFLVVSSFAVFTPSAAAETYTVKLGSDKGMLAFEPSKLTVKPGDTIKWVNNKVPPHNVVFDAAKNPAKSADLAKGLSHKQLLMSPGQEFETTISADTPPGEYTFYCEPHRGAGMIGKLTVEG
>NZ_CP019636.1|WP_087543106.1|6287366_6287858_-|cytochrome-c-550
MFRRLFGIFAATILLTFQFFTGSATAVELDKATRTVPFNENGETVVLSLKQVKEGKRLFNYACAQCHAGGITKTNQNVGLDPETLALATPNRNNIEGLVDYMKNPTTYDGEEEISELHPSTKSADIFTEMRNLTDDDLEAIAGHILLQPKIIGEKWGGGKIYY
>NZ_CP019636.1|WP_087543109.1|6287980_6288196_-|hypothetical-protein
MGFADLSIAEIATDYSVPVEKVLSLCDKLLIAYKNPKTRLALEDAKAIISQILSERQPEGTNNSVGETEVT
>NZ_CP019636.1|WP_087543112.1|6288986_6289823_-|carbohydrate-ABC-transporter-permease
MTNVSRVSWLKVLLYAVLTLYAVITLIPFLWALSASFKPLSEIVRGGANFIPKNFTLDNYKQIFFQEPLFLRWLFNSVFIAVSVTVLNLLFNSMAGYALARLHFRGRRFWFFLILAVLAVPAQITLIPTFLILKALGWLNSYQGMIVPSMVNATFIFMMRQFFVNFPKELEEAAQLDGLNTWGIFRHIVLPLAKPALAAQAVFVFMGSWNNFLLPIVILFDPEMFTLPLGLNSFKGQFISYWNYIMAASMVFTLPALAIYAFFNRYFIESVTFTGGKG
>NZ_CP019636.1|WP_087546380.1|6289819_6290719_-|sugar-ABC-transporter-permease
MRRQRISTRSNLTEDLAGYLFMLPTILVLGTFVVLPILWAVFLSLHKVQLLGSIKYQFIGFRNFTRLIEDERVWIALKNTAEYVAIVVPIQTILALILAVTLNSGIRAKSWWRVLYFLPTVTSSAVLTLIFMWIYNTNGLLNDFLAFVGLPTYNWLGDPAVALKGIMLMNIWSTAPFYMVIYLAALQDIPRSLYEAASLDGANGWQQFIHITIPILKPVTFFVITMGVIGTFQLFDQSYIFSNGTGGPNNATLTVVLLIYQAVFRNLQMGYGAAIAFLLAAVIIVVTLIQRRFFGGEKF
>NZ_CP019636.1|WP_087546381.1|6291247_6291982_-|class-I-SAM-dependent-methyltransferase
MNEWYKEDLAFIHDAGFSDWALKSVPGILEILNRSQIQEGLIVELGCGSGLSAQEFTKADYKVLGIDISEAMVEIARTRVPDAEFRIESLFKADIPPCNAVISLSECLNYLFDPDNNSQTLIQLFYRIYNALIPGGVFIFDIAEPGQVISQTPIKNFTETDDWIVLVEKQEDRDSEILTRRIITFRKVGEHYRRDDEVHRQQLYKAADVTAKLRRVGFEVQTTQSYGQFHLPKAHTAFIAYKPA

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Crispr_ID: NZ_CP019636_20

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_20

6520695-6520845

Orphan

Consensus_repeat	Method
CAAATGTCTTAGAGCATCTCCCCGACGAAACCAAGCCCAGTAATCATCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_20

>merge|NZ_CP019636|20|6520695-6520845|CRISPRCasFinder
CAAATGTCTTAGAGCATCTCCCCGACGAAACCAAGCCCAGTAATCATCCCGTCGGATTGTGAGGGCTTCATCATAATCGGAAATTGCATCTTTAAAGCGCTTCAAATGTCTTAGAGCATCTCCCCGACGAAACCAAGCCCAGTAATCATCC

>NZ_CP019636|20|19|6520695-6520845|CRISPRCasFinder
CAAATGTCTTAGAGCATCTCCCCGACGAAACCAAGCCCAGTAATCATCC	CGTCGGATTGTGAGGGCTTCATCATAATCGGAAATTGCATCTTTAAAGCGCTT
CAAATGTCTTAGAGCATCTCCCCGACGAAACCAAGCCCAGTAATCATCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087543441.1\|6511022_6512087_+\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|187568
NZ_CP019636.1\|WP_087543458.1\|6525209_6525608_-\|DUF1636-domain-containing-protein	unknown	unknown	gnl\|CDD\|377928
NZ_CP019636.1\|WP_087543457.1\|6524346_6525198_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187554
NZ_CP019636.1\|WP_087543439.1\|6510127_6510946_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|369777
NZ_CP019636.1\|WP_087543470.1\|6534844_6536002_-\|DegT/DnrJ/EryC1/StrS-aminotransferase-family-protein	unknown	unknown	gnl\|CDD\|99740
NZ_CP019636.1\|WP_087543468.1\|6533793_6534687_-\|cyanoexosortase-B	unknown	unknown	gnl\|CDD\|275018
NZ_CP019636.1\|WP_087543451.1\|6518683_6520198_+\|C-3',4'-desaturase-CrtD	unknown	unknown	gnl\|CDD\|274272
NZ_CP019636.1\|WP_087543443.1\|6512200_6512617_+\|GtrA-family-protein	unknown	unknown	gnl\|CDD\|377229
NZ_CP019636.1\|WP_087543445.1\|6512654_6514307_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379080
NZ_CP019636.1\|WP_087543464.1\|6528872_6531032_-\|polysaccharide-biosynthesis-tyrosine-autokinase	unknown	unknown	gnl\|CDD\|349772
NZ_CP019636.1\|WP_087543466.1\|6532838_6533549_-\|cyanoexosortase-B-system-associated-protein	unknown	unknown	gnl\|CDD\|275326
NZ_CP019636.1\|WP_087543462.1\|6528380_6528857_+\|MEKHLA-domain-containing-protein	unknown	unknown	gnl\|CDD\|378025
NZ_CP019636.1\|WP_087543460.1\|6525852_6528147_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543433.1\|6506444_6507656_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133029
NZ_CP019636.1\|WP_087543449.1\|6517305_6518619_+\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340831
NZ_CP019636.1\|WP_087543447.1\|6514327_6515848_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133022
NZ_CP019636.1\|WP_087546395.1\|6531217_6532609_-\|sugar-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|224512
NZ_CP019636.1\|WP_087543455.1\|6521513_6524240_+\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|226702
NZ_CP019636.1\|WP_087543437.1\|6508997_6510020_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|132997
NZ_CP019636.1\|WP_087543435.1\|6507652_6508936_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133029

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087543441.1\|6511022_6512087_+\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|187568	cd05258, CDP_TE_SDR_e, CDP-tyvelose 2-epimerase, extended (e) SDRs. CDP-tyvelose 2-epimerase is a tetrameric SDR that catalyzes the conversion of CDP-D-paratose to CDP-D-tyvelose, the last step in tyvelose biosynthesis. This subgroup is a member of the extended SDR subfamily, with a characteristic active site tetrad and NAD-binding motif. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. 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. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. 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.	7.66423e-158
NZ_CP019636.1\|WP_087543458.1\|6525209_6525608_-\|DUF1636-domain-containing-protein	gnl\|CDD\|377928	pfam07845, DUF1636, Protein of unknown function (DUF1636). The sequences featured in this family are derived from a number of hypothetical prokaryotic proteins. The region in question is approximately 130 amino acids long.	5.69832e-59
NZ_CP019636.1\|WP_087543457.1\|6524346_6525198_+\|SDR-family-oxidoreductase	gnl\|CDD\|187554	cd05243, SDR_a5, atypical (a) SDRs, subgroup 5. This subgroup contains atypical SDRs, some of which are identified as putative NAD(P)-dependent epimerases, one as a putative NAD-dependent epimerase/dehydratase. Atypical SDRs are distinct from classical SDRs. Members of this subgroup have a glycine-rich NAD(P)-binding motif that is very similar to the extended SDRs, GXXGXXG, and binds NADP. Generally, this subgroup has poor conservation of the active site tetrad; however, individual sequences do contain matches to the YXXXK active site motif, the upstream Ser, and there is a highly conserved Asp in place of the usual active site Asn throughout the subgroup. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended 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.	2.62346e-51
NZ_CP019636.1\|WP_087543439.1\|6510127_6510946_+\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	2.66301e-26
NZ_CP019636.1\|WP_087543470.1\|6534844_6536002_-\|DegT/DnrJ/EryC1/StrS-aminotransferase-family-protein	gnl\|CDD\|99740	cd00616, AHBA_syn, 3-amino-5-hydroxybenzoic acid synthase family (AHBA_syn). AHBA_syn family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). The members of this CD are involved in various biosynthetic pathways for secondary metabolites. Some well studied proteins in this CD are AHBA_synthase, protein product of pleiotropic regulatory gene degT, Arnb aminotransferase and pilin glycosylation protein. The prototype of this family, the AHBA_synthase, is a dimeric PLP dependent enzyme. AHBA_syn is the terminal enzyme of 3-amino-5-hydroxybenzoic acid (AHBA) formation which is involved in the biosynthesis of ansamycin antibiotics, including rifamycin B. Some members of this CD are involved in 4-amino-6-deoxy-monosaccharide D-perosamine synthesis. Perosamine is an important element in the glycosylation of several cell products, such as antibiotics and lipopolysaccharides of gram-positive and gram-negative bacteria. The pilin glycosylation protein encoded by gene pglA, is a galactosyltransferase involved in pilin glycosylation. Additionally, this CD consists of ArnB (PmrH) aminotransferase, a 4-amino-4-deoxy-L-arabinose lipopolysaccharide-modifying enzyme. This CD also consists of several predicted pyridoxal phosphate-dependent enzymes apparently involved in regulation of cell wall biogenesis. The catalytic lysine which is present in all characterized PLP dependent enzymes is replaced by histidine in some members of this CD.	3.04968e-130
NZ_CP019636.1\|WP_087543468.1\|6533793_6534687_-\|cyanoexosortase-B	gnl\|CDD\|275018	TIGR04156, eight_transmembrane_protein_EpsH, cyanoexosortase B. This model describes a cyanobacterial-restricted form of exosortase, associated with a PEP-CTERM domain subclass described in model TIGR04155. This is one of two such cyanoexosortases, either of which is sufficient to accompany TIGR04155 family members. The cyanoexosortase is TIGR03763. [Protein fate, Protein and peptide secretion and trafficking].	4.65488e-175
NZ_CP019636.1\|WP_087543451.1\|6518683_6520198_+\|C-3',4'-desaturase-CrtD	gnl\|CDD\|274272	TIGR02733, similar_to_to_phytoene_dehydrogenase, C-3',4' desaturase CrtD. Members of this family are slr1293, a carotenoid biosynthesis protein which was shown to be the C-3',4' desaturase (CrtD) of myxoxanthophyll biosynthesis in Synechocystis sp. strain PCC 6803, and close homologs (presumed to be functionally equivalent) from other cyanobacteria, where myxoxanthophyll biosynthesis is either known or expected. This enzyme can act on neurosporene and so presumably catalyzes the first step that is committed to myxoxanthophyll. [Biosynthesis of cofactors, prosthetic groups, and carriers, Other].	0
NZ_CP019636.1\|WP_087543443.1\|6512200_6512617_+\|GtrA-family-protein	gnl\|CDD\|377229	pfam04138, GtrA, GtrA-like protein. Members of this family are predicted to be integral membrane proteins with three or four transmembrane spans. They are involved in the synthesis of cell surface polysaccharides. The GtrA family are a subset of this family. GtrA is predicted to be an integral membrane protein with 4 transmembrane spans. It is involved is in O antigen modification by Shigella flexneri bacteriophage X (SfX), but does not determine the specificity of glucosylation. Its function remains unknown, but it may play a role in translocation of undecaprenyl phosphate linked glucose (UndP-Glc) across the cytoplasmic membrane. Another member of this family is a DTDP-glucose-4-keto-6-deoxy-D-glucose reductase, which catalyzes the conversion of dTDP-4-keto-6-deoxy-D-glucose to dTDP-D-fucose, which is involved in the biosynthesis of the serotype-specific polysaccharide antigen of Actinobacillus actinomycetemcomitans Y4 (serotype b). This family also includes the teichoic acid glycosylation protein, GtcA, which is a serotype-specific protein in some Listeria innocua and monocytogenes strains. Its exact function is not known, but it is essential for decoration of cell wall teichoic acids with glucose and galactose.	2.27664e-11
NZ_CP019636.1\|WP_087543445.1\|6512654_6514307_+\|hypothetical-protein	gnl\|CDD\|379080	pfam13231, PMT_2, Dolichyl-phosphate-mannose-protein mannosyltransferase. This family contains members that are not captured by pfam02366.	5.36515e-05
NZ_CP019636.1\|WP_087543464.1\|6528872_6531032_-\|polysaccharide-biosynthesis-tyrosine-autokinase	gnl\|CDD\|349772	cd05387, BY-kinase, bacterial tyrosine-kinase. Bacterial tyrosine (BY)-kinases catalyze the autophosphorylation on a C-terminal tyrosine cluster and also phosphorylate endogenous protein substrates by using ATP as phosphoryl donor. Besides their capacity to function as tyrosine kinase, most of these proteins are also involved in the production and transport of exopolysaccharides. BY-kinases are involved in a number of physiological processes ranging from stress resistance to pathogenicity.	1.00927e-41
NZ_CP019636.1\|WP_087543462.1\|6528380_6528857_+\|MEKHLA-domain-containing-protein	gnl\|CDD\|378025	pfam08670, MEKHLA, MEKHLA domain. The MEKHLA domain shares similarity with the PAS domain and is found in the 3' end of plant HD-ZIP III homeobox genes, and bacterial proteins.	9.01902e-71
NZ_CP019636.1\|WP_087543466.1\|6532838_6533549_-\|cyanoexosortase-B-system-associated-protein	gnl\|CDD\|275326	TIGR04533, cyanosortB_assc, cyanoexosortase B-associated protein. Members of this protein family are found exclusively in the Cyanobacteria, usually encoded next to a gene encoding cyanoexosortase B (TIGR04156). This relationship resembles the association of the unrelated protein family TIGR04153 with cyanoexosortase A (TIGR03763), and of most exosortases with EpsI.	1.09545e-119
NZ_CP019636.1\|WP_087543433.1\|6506444_6507656_+\|glycosyltransferase	gnl\|CDD\|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	9.38652e-29
NZ_CP019636.1\|WP_087543449.1\|6517305_6518619_+\|glycosyltransferase-family-4-protein	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct 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. The members of this family are found mainly in certain bacteria and archaea.	3.1737e-46
NZ_CP019636.1\|WP_087543447.1\|6514327_6515848_+\|glycosyltransferase	gnl\|CDD\|133022	cd04179, DPM_DPG-synthase_like, DPM_DPG-synthase_like is a member of the Glycosyltransferase 2 superfamily. 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. In higher eukaryotes,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. In lower eukaryotes, such as Saccharomyces cerevisiae and Trypanosoma brucei, DPM synthase consists of a single component (Dpm1p and TbDpm1, respectively) that possesses one predicted transmembrane region near the C terminus for anchoring to the ER membrane. In contrast, the Dpm1 homologues of higher eukaryotes, namely fission yeast, fungi, and animals, have no transmembrane region, suggesting the existence of adapter molecules for membrane anchoring. This family also includes bacteria and archaea DPM1_like enzymes. However, the enzyme structure and mechanism of function are not well understood. The UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate. This protein family belongs to Glycosyltransferase 2 superfamily.	6.7315e-48
NZ_CP019636.1\|WP_087546395.1\|6531217_6532609_-\|sugar-ABC-transporter-substrate-binding-protein	gnl\|CDD\|224512	COG1596, Wza, Periplasmic protein involved in polysaccharide export, contains SLBB domain of b-grasp fold [Cell wall/membrane/envelope biogenesis].	2.12595e-29
NZ_CP019636.1\|WP_087543455.1\|6521513_6524240_+\|GAF-domain-containing-protein	gnl\|CDD\|226702	COG4251, COG4251, Bacteriophytochrome (light-regulated signal transduction histidine kinase) [Signal transduction mechanisms].	7.79691e-38
NZ_CP019636.1\|WP_087543437.1\|6508997_6510020_+\|glycosyltransferase	gnl\|CDD\|132997	cd00761, Glyco_tranf_GTA_type, Glycosyltransferase family A (GT-A) includes diverse families of glycosyl transferases with a common GT-A type structural fold. Glycosyltransferases (GTs) are enzymes that synthesize oligosaccharides, polysaccharides, and glycoconjugates by transferring the sugar moiety from an activated nucleotide-sugar donor to an acceptor molecule, which may be a growing oligosaccharide, a lipid, or a protein. Based on the stereochemistry of the donor and acceptor molecules, GTs are classified as either retaining or inverting enzymes. To date, all GT structures adopt one of two possible folds, termed GT-A fold and GT-B fold. This hierarchy includes diverse families of glycosyl transferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. The majority of the proteins in this superfamily are Glycosyltransferase family 2 (GT-2) proteins. But it also includes families GT-43, GT-6, GT-8, GT13 and GT-7; which are evolutionarily related to GT-2 and share structure similarities.	2.16016e-22
NZ_CP019636.1\|WP_087543435.1\|6507652_6508936_+\|glycosyltransferase	gnl\|CDD\|133029	cd04186, GT_2_like_c, Subfamily of Glycosyltransferase Family GT2 of unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	9.07484e-28

>NZ_CP019636.1|WP_087543451.1|6518683_6520198_+|C-3',4'-desaturase-CrtD
MPGHRIGKNKSHVIVIGAGIGGLTAGALLARRGYSVLILDQALVPGGCASTFKRKGFTFDVGATQVAGLEPGGIHHRIFTELEIDLPEATPCDPACAVYLPGEETPINVWRDPDKWKEERQQQFPGSEPFWQLMAALFKASWEFQGRDPVLPPRNLWDLLQLTKAVRPSTFKTVPYTLFTVGDALRAYKLGNNQRLKTFLDLQLKLYSQVSAEETALLYAATALSVSQLPQGLYHLQGSMQVLSDRLVEALEKNGGKLLMRHTVEHIKVEKGNVSAVVIRNQKTGEVWTEPADHVVANVTAQNLVQLLGNKAPKGYKQRVKKLPAASGAFVVYLGVDESAIPPGCPPHLQFMYDAKGPIGENNSLFVSVSHPGDGRAPHGKATIIASSFVETQQWWQTEDYEGLKQQYTQDAISHLAKFFYLKPETIIHVEAATPRTFAHYTARDRGIVGGIGQRISTFGPFGFANRTPINNLWLVGDSTHPGEGTAGVSYSALTAVKQIQAQE
>NZ_CP019636.1|WP_087543449.1|6517305_6518619_+|glycosyltransferase-family-4-protein
MNTQTQPTIALLHWGDLIEDFLDTIGVSFESFCNEMTGGWLFGYIDALRLVGVQTVLFCISARVTEVMRYTHQPTGATICVLPVPKIYQLARRPMLNPYGWTVTDVFGDVHGIRRRLLGLLRDVAPYLATPLRLLAHELRREGCQAILCQEYEYARFDACVLLGQLMRLPVFATFQGGDFQLSRLERPLRPLTIKACAGLIVATQTEVQRVQSHYGVPSTKLARIFNPMDVANWHAMDRSQARVALGIPLNAQVVIYHGRVDIHRKGLDILLDAWQQVLCDRPERDLRLLLVGTGSDADKLRQRLAQMQLAGVMWTDEYVRDRTVIQRYLSAADVYTLPSRHEGFPVAPIEAMSCSLPVVATDAPGVPDIFEGGEVSGGLVVPRGDATALALALGRMLDNETWMRELGKLARCRAEECFSLEAIGQQLHDFFMSRGI
>NZ_CP019636.1|WP_087543447.1|6514327_6515848_+|glycosyltransferase
MSKQVVITEPDFQSIKTLGIRETYRDQYWLKQDPIYEDRLLWRAQTFRHIVHLLPGQTILELGCGEGHFTRQLLRVSREQNPITAVTFHSDNHRPKDFPAFVEFTNASSVFETLAGRSFDFIIAMDLLDERNCGWLLQKINELLKPGGQVIFYESNPWNVVLKLRRFISQLLGRKDPRRLLSRSKLYELISEVGFLRVFAVHNDFVYAPLTRSLVWFLRNLSILLENTPGIQNLAGSILIHAQKPPRVVERPKISLFEHEQLRKSVSVVIPCHNEEMNVEPLVNKLRDFYGEYIHEIIPVDDNSRDNTAEVIQRLAQEDPIIKPVFRSPPNGVGRAITDGYQVATGKYILSMDCDFQHLLPEIRDLFDAAAEGYDVVVGSRFSRHSVLLNYPLQKIIANRGFHALAQILFQQRFRDLTNNLKLIRREVIEKIEWTQPGFAINAETGLEPLLRGYSVKEVPISWINRTPDMGVSSFRLIKVGNGYWRVLLRLWLRTAFGIGRQHPQK
>NZ_CP019636.1|WP_087543445.1|6512654_6514307_+|hypothetical-protein
MNKKNKILANLEYIVPIIASISLLISCLVISPKKYFWNDELYSYYFLADSSFTKMMVAFHDKINNTPPLYFILGWLWARVFGSTELSLRLFSSLGMCIACVTVWITLRRTYNFWSASIGTLAVFCTSDIILDQNAEARMYGLFLATSSLALLYFDVLNRIPEFSWRIWLFNFFIHDAIVQTHLFGLFYSGAVLFSLIIRDRCLNIFRAKIYLSIVLSWFSLILYIPSFLNQADAGKPRTWVPTPTSQDLLNLINLSSSSFLNLFVLFLLVLISGLLFIGETESTRASLVGQQNTPNTKAETSLLIFAYIFLAVPVFVWMISRTVKPIFWDRYMIPSTLGWAILLASLSSRIILSNKNSNNFRISRFLVFTQKTILLLVLCTILLIHPISYAKSYQRQYLPGLNDNKYGYRQLPIVVQASAQFLKRLHYSPERNRYFFILDWQAAVDDASGQFSPQEYKHLDALKRNYPKLFQNQILQSQDFLKKYNSFLVLDYLDYKKKCPIKAKGSKWDNIHCPQWLEMRILRNSDYQVKHLGEVYDESLLLVENRKKI
>NZ_CP019636.1|WP_087543443.1|6512200_6512617_+|GtrA-family-protein
MLKKLFQKKIFRFIICGAITAAFNIVLIYSMIEYLKLNTPLLRNVANILSLEVSLVFSFFVYKVWVWSGSPWKIKEVLLRQMPLYHLSVFACVITRSCVLFPILDWIKINYLVNTLIGILIGSIINYLMSDKFVFKTN
>NZ_CP019636.1|WP_087543441.1|6511022_6512087_+|NAD-dependent-epimerase/dehydratase-family-protein
MNIILVTGAAGLIGSESVRFFCERGFTVVGIDNNMRACFFGEEASTEWNRDRLLQDYGDQYIHYNVDIRNQEEIAKVFKTYNKDISLIIHTAAQPSHDWAAKDPYTDFTVNANGTLVLLENTRQICPEAVFIFCSTNKVYGDTPNFLPLVEQELRWEIEQTHPYSNGIDESMSIDSCKHSLFGASKVAADILVQEYGRYFAMKTATFRGGCLTGPSHAGTKLHGFLSYLIKCTITGKPYQVYGYQGKQVRDNIHSYDLVNAFYHFYQAPRVAEVYNIGGSRFSNCSMLEAIQNCEAITEKKLNWSYEESNRIGDHIWWISNIDKFKSHYPNWELTYTITDILKEIFTQNISRWV
>NZ_CP019636.1|WP_087543439.1|6510127_6510946_+|class-I-SAM-dependent-methyltransferase
MQTLSPKQNVAYKAPLGEFLSRNPFPEPLTQGFFYREKMRAIHRITPDKPFQDILEVGGGQSGLTALLFPQAQVTNLDLNPEYAQAPCNQQQKVHFICGDATDLPFENQSFDAVTMFDLLEHVPDDKKAVSEALRVLRPGGFLLISTPNENWRFPYYKFMKPICPSEAEIMTEWGHVRRGYTLAELKTLINLPCQGYATFINPLTVLGHDVAFSCLSHRWRRFLCKALNPLTWLGYYLHNPQATGTETASAWQKSREDRQSLSNVIGESLAL
>NZ_CP019636.1|WP_087543437.1|6508997_6510020_+|glycosyltransferase
MSNLSLHPTDNHTSIDLVICTYNNAELLDRALIAISKQQVPDDIKWTVLVVNNNCTDETAQVVDRHIQSQKIPYLSTILEPKQGLNHARQCGVINTTGDWIAFVDDDCILEEDWVAQAGKFAAAHPHCGAFGGRVILDWETPPPAFVLKYGYSFAQQDHGMSLTQPNCLVGAGLVVNRKAVLATNWVSKQFLSDRVGKKLISGGDVEMVLRIRSAGYDIWYNPACKLMHFIPSRRIEQKYLININYGLGISQLMSDGLVWHSSFFNLLVLSVFSTFRSSIAVFVKALKVALGRGNMEVAEIAIIWAFVQGKWVGIGRMLRMDAQERRALLGSAKLVSSNN
>NZ_CP019636.1|WP_087543435.1|6507652_6508936_+|glycosyltransferase
MSTFAPWKIVHIELSEDIPELTAEPKYQGIYAVFWWCGVPLGDLEILAAQLPMPATQLANLIVQTITPVVGDRLLDYGFKAPLPVISQNPSRDTPVDFQALMALQQPLKQLHQSCSQPVSTSISVIVCTRNRPEQLARCLRSLQNLSQRPEQILVVDNAPADDATRQVVAQMPGIQYVLEPHPGLSVARNTGIRHSIGDIIAFTDDDTIVNPDWSIRLQQGFENPKVQAVTGLMLPAVLETEAQWIFHKSSGGPSWGYRALTFDTQFFEKTKHQGVPVWLIGAGANMAFRRKAFEIFGYFDERLGAGASGCSEDSEFWYRILAEGWLCRYEPTSVIFHYHRSDLDNFKHQMYQYMRGHVTALLVQFANYKHWGNLYRLFIALPKYYARRLLQDMKRGFQPKHSSVLAEIAGCVSGVKFYIDHVKILA
>NZ_CP019636.1|WP_087543433.1|6506444_6507656_+|glycosyltransferase
MSYSIIEIELTQPLPTISLSESETGIALILRRKDEPIGFLLQAQPANSVLTPENLAQLIAKEAGTKLLEESIRDELMVNTSFVQFPPLTVAICTKDRPENLARCLQSLLKIQTPALKLEILVIDNAPSNEDTKELVDSLQGVRYVREPKPGLDFARNCALHSATGELLAFVDDDVIVDRKWLEGLMEAWAENPDAAAFTGLVLPYELVTDAQILFEQRGGFRRGFDKIRYGQVLAGNPLHPCGAGIFGAGCNMAFRREILQKLGGFDEALDTGAPLPGGGDLDIFYRVIRAGYPLVYEPKYLVFHQHRREQEKLRRQYWTWGLGFMAFVAKSYQTDPPQRSQLRRLIWWWVKDQLQQLKNSLIGRHVLPPSMISAEFWGGMVGLFGEYPRSLRRIEQIRRKFS
>NZ_CP019636.1|WP_087543455.1|6521513_6524240_+|GAF-domain-containing-protein
MELTKNLHTWEEQFDEEGLLELHRITTQIKQSPELQEILAATVSEVRSFLKTDRVVVYRFDTNGSGEVIAESIHEERLPSLLGLHFGADDIPPGVRNMFLWARQRSIVDVASGFIGLSQLASPETGNSLPKENIYYREVDPCHIEYLKAMGVQSSVVVPILEYSSTEQSAKPQLWGLLISHHSEARTVLHRELQVVQLFVDQLAMAIAQTHLLTRIRAAQQQEAIVNQITNLLHPLSTNQLQTALEVTIAAIDGVGGRLYIEQSAELYSWGEQPRQVIEQHPVWQEWIAECQNGDIKATSDIYKEPSCQALAPFFQSTQIRGLLAIPLSYDNHFIGVLSIFRSEVETEILWAGRRELDEQQQNQISFEPWLEQKKEQAPEWKPEEITLAQALATQFSIAIQQQQVYQQVQTLNANLEHQVQERTSQLQQSLDQALVVKQVTDQIRSNLDYNITLQTIVKEVRQLLKADRVLIYKLHRDGGGEVIVEDVDIYWRSVLGQQMPQECFPDEYARLYFRGRVRAINNTSTAELDPCHQEFLQSLQIKANLIVPINISTQLWGLLIAHQCYAPRNWQDAEIDLLQQLADEAAIAIQQAQLYEKSRNAESTARAQAGQVTQLLHQMQQTQTKLIQTEKMSSFGLLALGAAHEINNSVNFICTKLSQASDYTQNLLELLDLYRLSYPQPNSEISYQAQAVNLDFLTQDLPQIMSSMKVQADRVRSTVQSFRNFSRLDQASTTPVDLNEGLDRALLILQRRLQSKVGSPGIKVIKDYGDLPLVECYAGQVNQVFMNILSYAIDALTEEIGEVGKVGEEMITTPSPSIRISTGVSSDHFRAVIRIAYNDLGMTQDIQKSIFDPVFMTKPLEKSTGMELAISYQIVVQKHGGVLNCVSEPEQGTEFWIEIPFKQTVSD
>NZ_CP019636.1|WP_087543457.1|6524346_6525198_+|SDR-family-oxidoreductase
MTYQGTQVEDLVLVAGATGGVGQLVVSNLLELGFRVRILTRNAAKAQKMFNHKVEVAIGDIRDPSTLPAAMQDVTYIICCTGTTAFPSARWEFDRTPSLIEWVQLFLDPKNCEAKAKNSPSKVDAQGVSNIVAAAPRNLKRFVFVSSCGVLRKDQFPFRILNAFGVLDAKLKGEEALISSGLPYTIIRPGRLIDGPYTSYDLNTLLKAKTKGKFGVVLDTGDKLGGQTSRIDVAAACVECMQSPYCQGQDFELINQGPRPSVIDWEGLFSKLDKTSDSSRPQK
>NZ_CP019636.1|WP_087543458.1|6525209_6525608_-|DUF1636-domain-containing-protein
MESQHMMFICTTCASVWQGGKRVGVSGGEKLLQQLQELHSHWELHSEFAIQPVECMSACHRSCVISFAANGKFTYLFGDLSPDLSPSEIAGVLECASKYYAHPQGLLPWAERPEPLKKGILAKIPPIPVPMA
>NZ_CP019636.1|WP_087543460.1|6525852_6528147_-|hypothetical-protein
MNTNTTGSITSIIAKRLPLTEKIAGMEAELKSLDSAIQLLKQVDDPSVAGLLEEANLITLHSSINTELKTLIQLKERFCRKTLNIGVVGQAKQGKSRLLQSLTGLSSVEIPDGDGHHCTGVPSIIYNSTNEKTYVEVWFHSEQSFLDEVLTPYYEKLHIDDKPNTFDEFVAKPLPLLPIDRPEYAEQGAMYEQLAQYHRHLDKYRHLLQQSSPRRITKEEIREYVTQETPNGQRFFFNPFPVGDVTRLGSMRVRAATASVEALMQPPTVSVASPSEEGNSCATLSQHIAVRSVKIVCQFPNADVGQIAFVDLPGLGDTGICNEQHLVKILGQQVDAILFVRMPKSTGDSWTDIDIRLYDTARAAHVDVPIDLWSFMILNRTEADSRFRDNSKSCQELAQDIANKKMNVVECITANCANSQEAHEVLERVIDHLKGKLSDLDDKYVLLCEQRLNVLQNKVKSELKKVSKALDLATQDDIHGFALFEAKFQEIWQELTKNFEKLLKGLRQKREAVDIDFKKQLEVTLQACRSDTGIPSIQEIEQRFCIEKNYTIVYEKYLNEIRAHLSKHLLSLESGLQRSLDKVKLQVAKILIEQGRLGKLVQAQDSEFIEAIAAQMPDELIPGIPSKLKYGFQTLAEFELSYRGFLQHRIRKHLDGLSPNEPATLKLSTSQSAEQVLLNLKIAYAETVGKCEKALKDLLCEPSQAIYAIVEEFIDCILRDQDVESEWRIFLQDARGQIWQEFQHNGDRPQLQHELLDLPEINQT
>NZ_CP019636.1|WP_087543462.1|6528380_6528857_+|MEKHLA-domain-containing-protein
MDRPRQLPWQQETVIRHSQRLMQSFYYWTGRALLDASGSPEEIAQALFDAPFVLVSHGTQPDPIFNYGNRMALQLWELSWEEFTKMPSRKTAEEVVQKERNRLLAETTTKGFSHFSGIRVTSSGKRFEIQDGLLWNVISEEKHLFGQAAVYSKCTFVQ
>NZ_CP019636.1|WP_087543464.1|6528872_6531032_-|polysaccharide-biosynthesis-tyrosine-autokinase
MTPPIVKRYLIAFDKYKWIGLASFGLVVAGSMVVALQPQQSKYVASGALTYNRPPVSFSATGIEINQQGQELNEDILLSEQVIEVVAAKVNVQPKKITQNVVLKTPEKEPKTGEIRSTLIELQYKDSDRLRARQTLQELMQAMIQLSAEINTRRLKAIISKVNERLPQAKKELQAAERKLELYDRKERPAILAAENGSLLEAVTGSQIQQRQIQFTITGIDAQIRSLQDKLGLNVNQAYVSSALSADPIIANLRAQIYQTESQIEVLKKDLRPEHPTMVQLRRQKEGYETLLRQRGGEVVGGENGTAPLPTNVSVRSQSNLDPARQVLANQMVALQTQRETLQQQLRDLVKEEARLRQEYSLVPNKQLERSRLEQDVALKKAVYDQMQVKQTDARTAEAETVSSLGIARPPIVMANTQERLSVPVTLGVGSLLGLLVGGGVVFLLGSLEGTFKTKEDIRDSLKQREVPLLGEIPLMPVDGLNVTDVPVVLSPESLYLEFYEKFRSNLRRIGGKNFKVVLITSTSSSEGKTVSAYNLGIASARAGKRTLIVETDLRSPSRSASLRVAPEPDATVEPLRYYASLSECIRLVPDVENLYILPSPGPVRQSAAILESSEMRRLMEDVRQRFDLVILDTPPLGLSNDALLIQPYSDGIVLVTRPNYTQENVLSEAIDQLVESELGLLGAVIDGADITVSLPPSFVEPNSPPEEESQAVANGARR
>NZ_CP019636.1|WP_087546395.1|6531217_6532609_-|sugar-ABC-transporter-substrate-binding-protein
MREFNALASTGLYVGLFLVAIVQPVVAQTSPTREQKPGLTPAPVPLTPERQSPLQPPAPPTPPPGSTDFVAPGLQEGMSPQLNRYLLGPGDAVNVLVQRPPGRYRLGPGDAIAVSVLRFPDLSFQAIINPEGNIVVPLLGTVSLQGLSLEEAQEKIRSGYNRFVVDPIVTLSLVGPRPEFNFAAQIDPEGNIVVPQVGTVSLQGLTLEEAQEKIRLGLSRVLVDPVVSVSLAGQRAVQVTISGEVNRPGIYPITSPTPRVSDALFIAGGSATMADLRQVQVRRKLVDGAVVSQTIDLYTPLQNGGEIPNLRLQDGDAIIVPRRELANDDSYDRTLVSRSTLATPQIRIRVLNYAGGGIVTVPLPNGSTFIDVLSGINTDSANLSEIALIRYDPERGRAVKQTLNAKKALSGDVSQNVPLQDNDVVVVGRNLISRITSVLSTITRPFFDVRNFLEFFGVYDRYR
>NZ_CP019636.1|WP_087543466.1|6532838_6533549_-|cyanoexosortase-B-system-associated-protein
MISFSKFLKERLFSQAVVLFLLLLLLVMGAIPGYLTGRWQWREPPRVASLQELKHLRQKGLSLPGWQTIEQREQEIGGRKWSYQLIQKEGNQTKAVLLLLPQTGARDQPMVEWTEINSFWQWQVAQFRSADFTVKQPKAEMQANGETKVEARFFRASTNQQTFAVLQWYAWFNGGHSSPLPWFVVDQLAQWHKKRAPWVAVSILIPMEPLGQVETTWNEAKSVGQTVQAALMTGML
>NZ_CP019636.1|WP_087543468.1|6533793_6534687_-|cyanoexosortase-B
MQLQRQLKNVKNSPFINLSILGILLLLYAPLLLYWWEGWIKKSISIEHEYFSHGIIGLPFAAYLCWMNRKKWQRLPNNPHPLGAVLLVLGGIFYLSGVSEWVNISFPAILAGLCLWLKGVPGLKLQGFPLTLVLLATPTSVPYLITPYTLPLQSFIAGTAGFILSQIGMQVIVDGINIYVGGRIVEVAPYCAGLKMLFTTLYVGLMLLYWTGALSSRRKSLWFLSIAVLISVSANIVRNTLLSLFHGTGQEGAFHWLHDGWGGDLYSAVMLLVLVPTLNWIDKYFSEVPESQQEGGD
>NZ_CP019636.1|WP_087543470.1|6534844_6536002_-|DegT/DnrJ/EryC1/StrS-aminotransferase-family-protein
MNIKVPFVDLKLQHQPIQTQLQQAIQTVIEQGDFILGQALKDFETAFAAASGAEYGVGVASGTDAIALGLQACDISPGDEVILPANTFVATLIGVIRAGAKPIFVDCDPQTALIDLEAAARAVTPQTKAIIPVHLYGQMVSPRQLLDFSQTYKVLIFEDAAQAHLAEREGYRAGSVGTAAAFSFYPSKNLGAFGDGGILITRDSEVAQKMIRLRNYGAAQKYIHIESGTNSRLDTMQAAVLHQKLPYLPQWNRDRFNAAQKYDMELAPLASSGITPIQNHSTEGHIYHLYVIRVDHSCVVQRQQLQEELTAVGIQTGIHYPIPCHLQPAFTHLGYHVGDFPNAEMLANQILSLPMYPGLSHSQVKEVVDAIASSLHTEQQKLLLI

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Crispr_ID: NZ_CP019636_21

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_21

6558638-6558729

Orphan

Consensus_repeat	Method
CAAAGACTCAAGCGTGAGTATCAGAACCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_21

>merge|NZ_CP019636|21|6558638-6558729|CRISPRCasFinder
CAAAGACTCAAGCGTGAGTATCAGAACCTCATGAATCAGTATCAAAGACTTGTGAACAAGTAGCAAAGACTCAAGCGCGAGTATCAGAACCT

>NZ_CP019636|21|20|6558638-6558729|CRISPRCasFinder
CAAAGACTCAAGCGTGAGTATCAGAACCT	CATGAATCAGTATCAAAGACTTGTGAACAAGTAG
CAAAGACTCAAGCGCGAGTATCAGAACCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087543488.1\|6548674_6549766_-\|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN	unknown	unknown	gnl\|CDD\|184688
NZ_CP019636.1\|WP_087543511.1\|6563841_6564894_-\|dipeptide-epimerase	unknown	unknown	gnl\|CDD\|239435
NZ_CP019636.1\|WP_087543513.1\|6565156_6565705_+\|NUDIX-hydrolase	unknown	unknown	gnl\|CDD\|239516
NZ_CP019636.1\|WP_087543509.1\|6562817_6563858_-\|DUF1611-domain-containing-protein	unknown	unknown	gnl\|CDD\|225902
NZ_CP019636.1\|WP_087543496.1\|6551670_6552522_-\|prolipoprotein-diacylglyceryl-transferase	unknown	unknown	gnl\|CDD\|376615
NZ_CP019636.1\|WP_087543502.1\|6554439_6556101_+\|M48-family-metalloprotease	unknown	unknown	gnl\|CDD\|320692
NZ_CP019636.1\|WP_087543526.1\|6571029_6571398_-\|dihydroneopterin-aldolase	unknown	unknown	gnl\|CDD\|376737
NZ_CP019636.1\|WP_087543494.1\|6550697_6551486_-\|precorrin-4-C(11)-methyltransferase	unknown	unknown	gnl\|CDD\|225430
NZ_CP019636.1\|WP_087543520.1\|6567261_6568188_-\|ribokinase	unknown	unknown	gnl\|CDD\|238579
NZ_CP019636.1\|WP_087543492.1\|6550207_6550561_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366507
NZ_CP019636.1\|WP_087543490.1\|6549856_6550186_-\|methyltransferase	unknown	unknown	gnl\|CDD\|376440
NZ_CP019636.1\|WP_087546397.1\|6556172_6556982_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|372967
NZ_CP019636.1\|WP_087546396.1\|6548395_6548575_+\|replication-restart-DNA-helicase-PriA	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543524.1\|6569038_6570346_-\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP019636.1\|WP_087543522.1\|6568424_6568982_-\|sugar-O-acetyltransferase	unknown	unknown	gnl\|CDD\|100047
NZ_CP019636.1\|WP_087543498.1\|6552929_6553496_+\|pantetheine-phosphate-adenylyltransferase	unknown	unknown	gnl\|CDD\|234674
NZ_CP019636.1\|WP_087543507.1\|6559031_6562628_+\|phytase	unknown	unknown	gnl\|CDD\|226698
NZ_CP019636.1\|WP_087543516.1\|6565819_6566743_-\|nucleoside-hydrolase	unknown	unknown	gnl\|CDD\|239113
NZ_CP019636.1\|WP_087543518.1\|6566756_6567188_+\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|223663
NZ_CP019636.1\|WP_087543500.1\|6553537_6554083_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226127

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087543488.1\|6548674_6549766_-\|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN	gnl\|CDD\|184688	PRK14457, PRK14457, 23S rRNA (adenine(2503)-C(2))-methyltransferase RlmN.	0
NZ_CP019636.1\|WP_087543511.1\|6563841_6564894_-\|dipeptide-epimerase	gnl\|CDD\|239435	cd03319, L-Ala-DL-Glu_epimerase, L-Ala-D/L-Glu epimerase catalyzes the epimerization of L-Ala-D/L-Glu and other dipeptides. The genomic context and the substrate specificity of characterized members of this family from E.coli and B.subtilis indicates a possible role in the metabolism of the murein peptide of peptidoglycan, of which L-Ala-D-Glu is a component. L-Ala-D/L-Glu epimerase is a member of the enolase-superfamily, which is characterized by the presence of an enolate anion intermediate which is generated by abstraction of the alpha-proton of the carboxylate substrate by an active site residue and is stabilized by coordination to the essential Mg2+ ion.	8.78861e-127
NZ_CP019636.1\|WP_087543513.1\|6565156_6565705_+\|NUDIX-hydrolase	gnl\|CDD\|239516	cd03424, ADPRase_NUDT5, ADP-ribose pyrophosphatase (ADPRase) catalyzes the hydrolysis of ADP-ribose and a variety of additional ADP-sugar conjugates to AMP and ribose-5-phosphate. Like other members of the Nudix hydrolase superfamily, it requires a divalent cation, such as Mg2+, for its activity. It also contains a highly conserved 23-residue Nudix motif (GX5EX7REUXEEXGU, where U = I, L or V) which functions as a metal binding site/catalytic site. In addition to the Nudix motif, there are additional conserved amino acid residues, distal from the signature sequence, that correlate with substrate specificity. In humans, there are four distinct ADPRase activities, three putative cytosolic enzymes (ADPRase-I, -II, and -Mn) and a single mitochondrial enzyme (ADPRase-m). Human ADPRase-II is also referred to as NUDT5. It lacks the N-terminal target sequence unique to mitochondrial ADPRase. The different cytosolic types are distinguished by their specificities for substrate and specific requirement for metal ions. NUDT5 forms a homodimer.	3.08032e-48
NZ_CP019636.1\|WP_087543509.1\|6562817_6563858_-\|DUF1611-domain-containing-protein	gnl\|CDD\|225902	COG3367, COG3367, Uncharacterized conserved protein [Function unknown].	5.58103e-123
NZ_CP019636.1\|WP_087543496.1\|6551670_6552522_-\|prolipoprotein-diacylglyceryl-transferase	gnl\|CDD\|376615	pfam01790, LGT, Prolipoprotein diacylglyceryl transferase.	1.07507e-99
NZ_CP019636.1\|WP_087543502.1\|6554439_6556101_+\|M48-family-metalloprotease	gnl\|CDD\|320692	cd07333, M48C_bepA_like, Peptidase M48C Ste24p bepA-like, integral membrane protein. This family contains peptidase M48C Ste24p protease bepA (formerly yfgC)-like proteins considered to be putative metallopeptidases, containing a zinc-binding motif, HEXXH, and a COOH-terminal ER retrieval signal (KKXX). They proteolytically remove the C-terminal three residues of farnesylated proteins. They are integral membrane proteins associated with the endoplasmic reticulum and golgi, binding one zinc ion per subunit. In eukaryotes, Ste24p is required for the first NH2-terminal proteolytic processing event within the a-factor precursor, which takes place after COOH-terminal CAAX modification (C is cysteine; A is usually aliphatic; X is one of several amino acids) is complete. Mutation studies have shown that the HEXXH protease motif, which is extracellular but adjacent to a transmembrane domain and therefore close to the membrane surface, is critical for Ste24p activity. Several members of this family also contain tetratricopeptide (TPR) repeat motifs, which are involved in a variety of functions including protein-protein interactions. BepA has been shown to possess protease activity and is responsible for the degradation of incorrectly folded LptD, an essential outer-membrane protein (OMP) involved in OM transport and assembly of lipopolysaccharide. Overexpression of the bepA protease causes abnormal biofilm architecture.	3.95128e-64
NZ_CP019636.1\|WP_087543526.1\|6571029_6571398_-\|dihydroneopterin-aldolase	gnl\|CDD\|376737	pfam02152, FolB, Dihydroneopterin aldolase. This enzyme EC:4.1.2.25 catalyzes the conversion of 7,8-dihydroneopterin to 6-hydroxymethyl-7,8-dihydropterin in the biosynthetic pathway of tetrahydrofolate.	1.35822e-43
NZ_CP019636.1\|WP_087543494.1\|6550697_6551486_-\|precorrin-4-C(11)-methyltransferase	gnl\|CDD\|225430	COG2875, CobM, Precorrin-4 methylase [Coenzyme metabolism].	2.47599e-125
NZ_CP019636.1\|WP_087543520.1\|6567261_6568188_-\|ribokinase	gnl\|CDD\|238579	cd01174, ribokinase, Ribokinase catalyses the phosphorylation of ribose to ribose-5-phosphate using ATP. This reaction is the first step in the ribose metabolism. It traps ribose within the cell after uptake and also prepares the sugar for use in the synthesis of nucleotides and histidine, and for entry into the pentose phosphate pathway. Ribokinase is dimeric in solution.	2.36572e-129
NZ_CP019636.1\|WP_087543492.1\|6550207_6550561_-\|hypothetical-protein	gnl\|CDD\|366507	pfam01187, MIF, Macrophage migration inhibitory factor (MIF).	6.63895e-28
NZ_CP019636.1\|WP_087543490.1\|6549856_6550186_-\|methyltransferase	gnl\|CDD\|376440	pfam01035, DNA_binding_1, 6-O-methylguanine DNA methyltransferase, DNA binding domain. This domain is a 3 helical bundle.	1.6695e-29
NZ_CP019636.1\|WP_087546397.1\|6556172_6556982_+\|hypothetical-protein	gnl\|CDD\|372967	pfam14218, COP23, Circadian oscillating protein COP23. This family includes the circadian oscillating protein COP23 from Cyanothece sp. (strain PCC 8801). The levels of this peripheral membrane protein display a circadian oscillation.	1.85906e-35
NZ_CP019636.1\|WP_087543524.1\|6569038_6570346_-\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	9.03411e-64
NZ_CP019636.1\|WP_087543522.1\|6568424_6568982_-\|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).	1.25046e-99
NZ_CP019636.1\|WP_087543498.1\|6552929_6553496_+\|pantetheine-phosphate-adenylyltransferase	gnl\|CDD\|234674	PRK00168, coaD, phosphopantetheine adenylyltransferase; Provisional.	5.19896e-94
NZ_CP019636.1\|WP_087543507.1\|6559031_6562628_+\|phytase	gnl\|CDD\|226698	COG4247, Phy, 3-phytase (myo-inositol-hexaphosphate 3-phosphohydrolase) [Lipid metabolism].	3.08242e-138
NZ_CP019636.1\|WP_087543516.1\|6565819_6566743_-\|nucleoside-hydrolase	gnl\|CDD\|239113	cd02647, nuc_hydro_TvIAG, nuc_hydro_ TvIAG: Nucleoside hydrolases similar to the Inosine-adenosine-guanosine-preferring nucleoside hydrolase from Trypanosoma vivax. Nucleoside hydrolases cleave the N-glycosidic bond in nucleosides generating ribose and the respective base. Nucleoside hydrolases vary in their substrate specificity. This group contains eukaryotic and bacterial proteins similar to the purine specific inosine-adenosine-guanosine-preferring nucleoside hydrolase (IAG-NH) from T. vivax. T. vivax IAG-NH is of the order of a thousand to ten thousand fold more specific towards the naturally occurring purine nucleosides, than towards the pyrimidine nucleosides. .	3.84939e-112
NZ_CP019636.1\|WP_087543518.1\|6566756_6567188_+\|nucleoside-deaminase	gnl\|CDD\|223663	COG0590, CumB, Cytosine/adenosine deaminases [Nucleotide transport and metabolism / Translation, ribosomal structure and biogenesis].	2.23351e-46
NZ_CP019636.1\|WP_087543500.1\|6553537_6554083_+\|hypothetical-protein	gnl\|CDD\|226127	COG3599, DivIVA, Cell division initiation protein [Cell division and chromosome partitioning].	5.91909e-06

>NZ_CP019636.1|WP_087546397.1|6556172_6556982_+|hypothetical-protein
MLSQPLKFLFFSGLSLSFVLGHGAAFAQVRSSGDVVVPTSPGGSGTTSTTTTTTGTGNSSTTTTTTNTSTPTPIDSGNRFSCQFYNGQYTVMYQPESQPGQYFAWAIPRTLGGGWDIQKRCDTIAQRLETYRPDGLVELKTAVENRQNILCVTTETNPYCRIVLTVPPEKDPNVVRNSVFQNLASADSGQQTIGVNTYTSGNDELSNLGRAIFGGGKQPSASAKDPINLKPFLDRADGGTGAKLRNGVSLGRQQSNPQTSNRLNPKKFR
>NZ_CP019636.1|WP_087543502.1|6554439_6556101_+|M48-family-metalloprotease
MQRKWKSLLLAFSWVFLSVGTSILIILTQPITSSAKEPAASTQTDTTNTPSSQKPSVVVPTTSTETSETDKPTESPQPTPTPSITDSKKPESAAEAAPTPEEIARQQKLIEADKLYQEGQKVAAEKLYREVKQPFAKTTDTQQRKEAIVDPAQLSPGGQVYWREAEAGIASQMQTRTLVALELLVQKNPEFIPGHIRYAEALKQYGQEKKVLQVLETAATFYPNQPDLIKARVAALAEAKKWMEASLAARQFALLNPNDPQALDFTKLAEDNLKRYKSHIRRQIRGNAIANIITGTLGYAFTGSLVGPFSALDSSIMLLRGEGAIGESVAKQAKKQLNLVKDEAILGYVNEIGQKLANVAGRNEFKYEFFVIPQEDLNAFALPGGKIFINAGAIAKTNSEAELAGLIGHELSHVVLSHGFQLVTQGNLIANVTQYIPYGGTIGQLFALSYSRDMERQADNLGTRLITATGYAADGLHNLMVTLEKQQKNAPPSWLSSHPGGNERVRSLEELISQNNYNRYAYEGVARHAQMKEKAKQILKEEKERKDKKRRRR
>NZ_CP019636.1|WP_087543500.1|6553537_6554083_+|hypothetical-protein
MILAGVNIPLTRRTLVDEDKLLDQLDEIRLSLPEAFQEAAAIIAQKEEILLQAEEYGQQIVDAAQAKRSQILDESDIIRQAEREASELRRQVQQECDDMLQQTLEEIDRKRRACQQEIEEIRRQAVAEAEAIEQGADDYADSVLENIEQNLQDMLRIIRNGRQQLLPDSSLEDNSQFPKKK
>NZ_CP019636.1|WP_087543498.1|6552929_6553496_+|pantetheine-phosphate-adenylyltransferase
MIAIYPGSFDPITLGHLDIIQRGSRLFSQMVVAVVRNPNKSPLFTVQKRLEQIRLSTKHLTHVEVDAFDGLTVKYAQMRGAQVLVRGLRAISDFEVELQMAHTNKTLFNQIETVFLATSNEYSFLSSSVVKEIAKFGGSIDHLVPPHVALDIYQCYAQNNPVSNQITTEAIPPRKSLPMDSPSEKQRE
>NZ_CP019636.1|WP_087543496.1|6551670_6552522_-|prolipoprotein-diacylglyceryl-transferase
MAPDLSTLPLAFQFTSPGPILVKLGPLTIRWYGFLIACAVLIGVTLSQFLAKRRNVNPDLISDLSIWLVIAAIPAARLYYVLFQWSEYAQHPERIIAIWQGGIAIHGAIIGGVVAALMFAKIKQVSFWQLADLVAPSLILGQAIGRWGNFFNSEAFGSPTNLPWKLYIPLQHRPPELTNFEYFHPTFLYESLWDLMVFALLITLFFRSLSGKPALKIGTLSLVYLAAYSLGRLWIEGFRTDSLMLGPLRIAQVVSLVGIVFGLTGLAWLYIVKRPLPDVASTR
>NZ_CP019636.1|WP_087543494.1|6550697_6551486_-|precorrin-4-C(11)-methyltransferase
MGTKKTYKALEPAVYIVGAGPGDPDLLTVKAQKLLESADVILFADSLVPQEILQLCREDAEIIPTANKTLEEILPVMIERVRSHKSVVRLHSGDPSLYSAIHEQMHLLAKAEIPFEVIPGISAFQAAAAKLKVELTVPGLVQTIILTRISGRTEVPDKEELGTLAAHQASLCLYLSARHVEEAQAKLLEHYSAETPVAICYRLGWSNEKIRVVPLNQMANCTHAEKLIRTTLYVISPALSPASARSRLYHPEHSRLFRSSHQ
>NZ_CP019636.1|WP_087543492.1|6550207_6550561_-|hypothetical-protein
MPLIKVQTSVSTPVGEEIDAMLKSLSAKLAKHTGKPESYVMTAFEAGVPMTFGGTTDPVCYIEIKSVGTMKPDQTQAMSQDFCQEINKALGVPKNRIYIEFADAKGAMWGWNGTTFG
>NZ_CP019636.1|WP_087543490.1|6549856_6550186_-|methyltransferase
MSTHNIIYEIVRQIPKGRVATYGQVADLANLYGKARLVGYALYRVDISVSDVPWHRVINAKGEISQSPSRYGGDNLQRSLLEQEGVKFSPEGKINLREYLWQPSLNLDD
>NZ_CP019636.1|WP_087543488.1|6548674_6549766_-|23S-rRNA-(adenine(2503)-C(2))-methyltransferase-RlmN
MSAKSVSVLPSPKSHTLQQPNISIPPLLGASLEELTAWVQQQGQPAYRGKQLHDWIYQKGVRTLCDISVFPKQWRADVAEIPIGRSNIHYRSVASDDTVKYLLQLADGQIIESVGIPTEKRLTVCVSSQVGCPMACDFCATGKGGYKRNLARHEIVDQVLTVQEDFQQRVSHVVFMGMGEPLLNTDHLIGAIKSLNQDVGIGQRNLTVSTVGIRDRIRQLAQHQFQVTLAVSLHAPNQALREQLIPSARPYPIEDLLAECREYVEITGRRVTFEYILLAGVNDLPEHALELAQRLRGFQSHVNLIPYNPIQEADYKRPNQNRIQAFVKVLKQQQIAVSVRYSRGLEADAACGQLRAKNQTKLS
>NZ_CP019636.1|WP_087546396.1|6548395_6548575_+|replication-restart-DNA-helicase-PriA
MQIVQKIRCPNCGSEGERHYLSHSQLTRTQCPMCDYLMISCTRTGKVIEAYAPGIHAQR
>NZ_CP019636.1|WP_087543507.1|6559031_6562628_+|phytase
MGTTNTIRFSQFNASLNRTSEGQLATDLSTPDNAQAKAVAEIIQRSNPDVLLINEFDYYEAAPLEPVRLFQKNYLSVSQNGTTPVEYPYVYIAPSNTGISSGFDLNNDGTAVTDPGTRGYGDDAFGFGEFPGQYGMLLLSKYPIDTANVRTFQNFLWKDMPGSLLPTIALPDSNTPWYSQQEQDVLRLSSKSHWDVPIVVNGETIHALVSHPTPPTFDGLEDRNGKRNYDEIRFWSDYITPGKGDYIYDDDGQGGGLATGSRFVIMGDQNADPFDGDSYNNAIRQLLLNPNINTNFIPSSLGGPQQTELQGGANLNHRGNSAFDTADFADTAPGNLRTDYVLPSTDLQISNSSVFWPLNTDPAFGLVGTFNSSLPGGFPSSDHRLVWADLQVPPTKAGRTIPNVDFSGQTIFPTGFIPSGNAGNVNGTEVPVGGLSGVTYDAANNRFYTISDDRSQFAPARFYTFTLETPSPQATDLAVTFTDVTTLKDEDGNDFPLNSLDPEGIALSKNHTVFISSEGEVNFNAGRVTNPFVNEFSLTTGQQLRSLPVPSKFLPVVQDTNGNGVTDAGDTQVSGVRNNLAFESLTISPDQKTLYTATESALLQDGPIATLTDGSRSRILQYNLVSGQPEKEYLYNTDAIAAQPNPVTGSADNGLVDLLALDNRGTLLALERSFAAGVGNTIKIYEVSLQGATDIKYYDSLNNLSAEQLADIKPAQKRLLLNLNSLNLPTGTDNIEGIAFGPQLADGRQSIVLVSDNNFSQTQFTQILALGADLVPTVAPTVETRPDLFDDPSLPTDQRADADDPAIYVNATNPEQSLVLTAVKNAGLRVYDLSGNLLQEVNPGSIRYNNIDLQYGFHLGNDSVDIAVATDRNNDKLAIFKINPYPNASGQYLEDITDSSIGTLFQASPYEPLYSASSRSAYGIALYHSPVTDDYYVFANRRQTGDVTQYKLIDTGNGKIGAERVRNFTVPTIAGRDPQLEGMVADQELGFLYIGQEDVGIWKYQAEPNADKTGTLIDKVKDIGGSYLEDDVEGLSIYYGKDGTGYLLTSSQGDNTFAVYTREGQNDFLGRFAVGNNGAIDSVQESDGADVINVPLGSNFPYGVFITQDGSNEPARLINDDGEISNVNSNFKLVPWENIAYAFPNPLTIDTSSYNPRTPNTSLLNGVASGAVPQPSSVLWTGSNLTGDVTFEQSFTGL
>NZ_CP019636.1|WP_087543509.1|6562817_6563858_-|DUF1611-domain-containing-protein
MRLALNQRVAILLHEGIKGPYGKTGLSLLRYSEAPIVAAIDRECEGKSLQELTGIKRNVPIVASVAAALEYKPQVLVIGIAPKGGTVPDDYWHEIKDAVSAGMSVVNGLHTPLATIPELKALLKPGQLIWDVRKEPPNLGIASGLARNLPCRRVLTVGTDMSVGKMSTSLELHWASRLRNWRSKFLATGQTGLMLEGDGVPLDAVRVDYAAGAVEQMVLRYGKNYDILHIEGQGSLLHPGSTATLPLIRGSQPTQMILVHRAGQIEVLPGVSIPPLAEVVKLYEAIATAGGAFAPVPVVGISLNTRHLDESEALDAIAQVEAETGLPCTDPVRFGASKLLDAVMQG
>NZ_CP019636.1|WP_087543511.1|6563841_6564894_-|dipeptide-epimerase
MQLKVEIFTINKRFPLTISRGTTAQTTNIWVRIAHDGIEGWGEASPFSVGIHPQSTETIKDALLQIAPSLQEFSPLQRASIDQVLNKALLPSSAKAALDMAMHDWLGKRVGLPLWQIWGLDRNAIVPTSMTIGINSPEGARARARDWLQLTEVRVFKVKLGSPDGIAADQKMLMAVREEAPEPKLYVDANGGWSLEDAVQMCNWLADLDVKYVEQPLPRGQEDNLAELKKRISLPIFVDESCFTSSDIPKLASCVDGINIKLMKSGGLTEAMRMVHTARAHGLQVMFGCYSDSTLANTAAAQLAPLADYLDLDSHLNLIDDPFTGAYVQEGRIFPNDLPGLGVKDSASGA
>NZ_CP019636.1|WP_087543513.1|6565156_6565705_+|NUDIX-hydrolase
MTNLQKWKLLHSKMVLNHHWCQVRQDEIQLPNGKIIDDYFVNIKPEVALILPITSRKEIIFVRQYRHAVGEFFIELPAGSFDPEEESAEEAALRELQEETGYVAQQVTKIATLYDKPSKDTNKIHLFLSENVMKSGEQNLDITEEIEVLLIPVESVQDKILNGEICVAGTVSALCLGLNFLK
>NZ_CP019636.1|WP_087543516.1|6565819_6566743_-|nucleoside-hydrolase
MSKQLVLMDHDGGVDDYLATMLLMTMDHIQPLGVVVTPADCYAEPAVSATRKILDLMGYSHILVAQSTVRGINPFPRLYRRDSFVIDHLPILNQSDTISTPLVAEPGQDFMIRVLREAPEPVTLMVTGPLTTVATALEKAPEIEAKIQRIVWMGGALNVTGNVEKNWEPGQDGSAEWNVYWDPISAARVWQTKIEIIMCPLDLTNTVPVTSDVVYKMGKQRHYPISDLAGQCYALVIPQDYYFWDVLATAYLAHPEFYQLREWKTEIITTGLSQGRTKIVPGGRKIYAMDKVDKEAFYTYILQQWAR
>NZ_CP019636.1|WP_087543518.1|6566756_6567188_+|nucleoside-deaminase
MDEFMQAAIAQAKQGRQEGGIPIGSVLVKDGKILGRGHNKRVQDGDPVTHAEIDCLRNAGRIGSYRGTTLYSTLMPCYLCAGAVVQFGIKKVIAGESRTFPGAKEFMVSHGVEVVDLNLDECEQMMSEFIQEKPELWNEDIGK
>NZ_CP019636.1|WP_087543520.1|6567261_6568188_-|ribokinase
MSIIVFGSINIDLVATAPRLPVAGETLLGHDFFKVPGGKGANQAVASARLGIPTDMVGRIGADSFGAELVNSLQASGVQTDNIVVDETISSGVAVIAVDVRGENQIVVVPGANGCVNQEDVERLSRLLPDAKAVLLQFEIPLPAVVAAAKVATEAGVTVILDPAPVQKEVPSELYRLVDIMTPNEVEAGQLVGFPVDGEESGKKAAAVLQQRGVKNVIVKLGAKGVVCATPEKTFFLPAFPVHTVDTTAAGDAFNGGLAAALHEGLSLHQAVVWGAAAGALATTKPGAQPSLPDRLRFDAFFKEKGAM
>NZ_CP019636.1|WP_087543522.1|6568424_6568982_-|sugar-O-acetyltransferase
MEKTEKQKMLAGELYLSSDAEIAAERNVARRLLRMYNSTTEEQLEQREQILQELFSYLGSNAEILPPFYCDYGKNIYAGDKLFMGIGCVILDCNTVHIGDNVLCAPYVQIYTAYHPTDPEIRLSGGELAAPIRIGNNVWIGGGAIICPGVTIGDNTTIGAGSVVVKDIPANVVAVGNPCRVVREL
>NZ_CP019636.1|WP_087543524.1|6569038_6570346_-|diguanylate-cyclase
MPSPTILVVENEKKTALDIKRRLQNLGYFTTEITFSGEEALKKVKEKNPILVLVDICLSGTINGTQVAEIIMNNFQVPVLYLTDTSKIKTINKNSIVEPFSYITKPVAEQDLYFAIEIALCKHQTKRKLQEEKQKFMSIIKSMGCAVIITDTHGCIHMMNPMAEEITGWKQDEAMTKSLAEVLSLVDKDTGAIIKDLATHVIKAGVVLNLPETFTLIAKDGTEIHIEGSITSILDDDKIIGAVLVFQDITLRKQIEAQLVRNAFYDALTALPNRVLFFERLRQVFERGKRRSNYHYAVLFLDLDGFKTINDSFGHSVGDNLLVEIARRLESCLRSGDTVSRFGGDEFAILIEDIRDVSDATNVAKRIQHTLSLPLYLDKHQISIAASIGIALNYSGYEKPESLLRDADMAMYHAKEQGKACYVVFNAQRLLDTYD
>NZ_CP019636.1|WP_087543526.1|6571029_6571398_-|dihydroneopterin-aldolase
MDCIHLTGIRCYGYTGYLQEEQVLGQWFEVDVRLWLDISKAGTTDAIEDTIDYRSIISLVQNLVKTSKFSLVEKLASTIADSVLASSDHATKVQVVLSKPAAPIPDFGGRISIELTRTKCNA

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Crispr_ID: NZ_CP019636_22

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_22

6760309-6760409

Orphan

Consensus_repeat	Method
GCGAGTGCGTCTGGTGATAGGAGAAGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_22

>merge|NZ_CP019636|22|6760309-6760409|CRISPRCasFinder
GCGAGTGCGTCTGGTGAACGCGAGTGCGTCTGGTGATAGGAGAAGGGTAGCGACGTCAGGAGCCTCTCCCGAAGCGAGTGCGTCTGGTGATAGGAGAAGGG

>NZ_CP019636|22|21|6760309-6760409|CRISPRCasFinder
GCGAGTGCGTCTGGTGAACGCGAGTGCG	TCTGGTGATAGGAGAAGGGTAGCGACGTCAGGAGCCTCTCCCGAA
GCGAGTGCGTCTGGTGATAGGAGAAGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087543821.1\|6758182_6759505_-\|D-alanyl-D-alanine-carboxypeptidase	unknown	unknown	gnl\|CDD\|224938
NZ_CP019636.1\|WP_087543827.1\|6762155_6763148_+\|beta-ketoacyl-ACP-synthase-III	unknown	unknown	gnl\|CDD\|236475
NZ_CP019636.1\|WP_087543800.1\|6741774_6743253_-\|leucyl-aminopeptidase	unknown	unknown	gnl\|CDD\|234863
NZ_CP019636.1\|WP_087543830.1\|6763430_6764309_+\|ACP-S-malonyltransferase	unknown	unknown	gnl\|CDD\|223408
NZ_CP019636.1\|WP_157679672.1\|6746345_6750308_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|226702
NZ_CP019636.1\|WP_087543833.1\|6764774_6765413_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP019636.1\|WP_087546413.1\|6756674_6757931_+\|LPS-export-ABC-transporter-periplasmic-protein-LptC	unknown	unknown	gnl\|CDD\|275202
NZ_CP019636.1\|WP_157679673.1\|6763222_6763393_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543803.1\|6745858_6746335_-\|response-regulator	unknown	unknown	gnl\|CDD\|381108
NZ_CP019636.1\|WP_087543846.1\|6768814_6769915_-\|tocopherol-cyclase	unknown	unknown	gnl\|CDD\|372979
NZ_CP019636.1\|WP_087543816.1\|6755655_6756288_+\|NYN-domain-containing-protein	unknown	unknown	gnl\|CDD\|350235
NZ_CP019636.1\|WP_157679729.1\|6765640_6765727_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543824.1\|6761017_6762043_+\|phosphate-acyltransferase-PlsX	unknown	unknown	gnl\|CDD\|235414
NZ_CP019636.1\|WP_087543838.1\|6766984_6767287_+\|DUF2288-family-protein	unknown	unknown	gnl\|CDD\|227913
NZ_CP019636.1\|WP_087543840.1\|6767515_6768046_-\|YdcF-family-protein	unknown	unknown	gnl\|CDD\|99750
NZ_CP019636.1\|WP_087543812.1\|6753905_6755507_+\|methionine--tRNA-ligase	unknown	unknown	gnl\|CDD\|237012
NZ_CP019636.1\|WP_087543806.1\|6750557_6751784_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226125
NZ_CP019636.1\|WP_087543836.1\|6765804_6766842_+\|AI-2E-family-transporter	unknown	unknown	gnl\|CDD\|223701
NZ_CP019636.1\|WP_087543809.1\|6752801_6753533_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP019636.1\|WP_087546412.1\|6751898_6752711_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087543821.1\|6758182_6759505_-\|D-alanyl-D-alanine-carboxypeptidase	gnl\|CDD\|224938	COG2027, DacB, D-alanyl-D-alanine carboxypeptidase (penicillin-binding protein 4) [Cell envelope biogenesis, outer membrane].	3.00124e-64
NZ_CP019636.1\|WP_087543827.1\|6762155_6763148_+\|beta-ketoacyl-ACP-synthase-III	gnl\|CDD\|236475	PRK09352, PRK09352, beta-ketoacyl-ACP synthase 3.	1.06342e-178
NZ_CP019636.1\|WP_087543800.1\|6741774_6743253_-\|leucyl-aminopeptidase	gnl\|CDD\|234863	PRK00913, PRK00913, multifunctional aminopeptidase A; Provisional.	0
NZ_CP019636.1\|WP_087543840.1\|6767515_6768046_-\|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.	1.12061e-27
NZ_CP019636.1\|WP_157679672.1\|6746345_6750308_-\|PAS-domain-S-box-protein	gnl\|CDD\|226702	COG4251, COG4251, Bacteriophytochrome (light-regulated signal transduction histidine kinase) [Signal transduction mechanisms].	2.60873e-58
NZ_CP019636.1\|WP_087543833.1\|6764774_6765413_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	1.10167e-55
NZ_CP019636.1\|WP_087546413.1\|6756674_6757931_+\|LPS-export-ABC-transporter-periplasmic-protein-LptC	gnl\|CDD\|275202	TIGR04409, LptC_YrbK, LPS export ABC transporter periplasmic protein LptC. Members of this family are LptC, a periplasmic protein tethered to the inner membrane in the lipopolysaccharide (LPS)exporter transenvelope complex (Lpt), which is responsible for conducting LPS to the outer leaflet of the outer membrane in most Gram-negative bacteria. LptC is homologous to LptA, another member of the transenvelope complex. Genes lptC and lptA are often adjacent. [Cell envelope, Biosynthesis and degradation of surface polysaccharides and lipopolysaccharides, Transport and binding proteins, Other].	1.38767e-11
NZ_CP019636.1\|WP_087543830.1\|6763430_6764309_+\|ACP-S-malonyltransferase	gnl\|CDD\|223408	COG0331, FabD, (acyl-carrier-protein) S-malonyltransferase [Lipid metabolism].	2.56501e-107
NZ_CP019636.1\|WP_087543803.1\|6745858_6746335_-\|response-regulator	gnl\|CDD\|381108	cd17557, REC_Rcp-like, phosphoacceptor receiver (REC) domain of cyanobacterial phytochrome response regulator Rcp and similar domains. This family is composed of response regulators (RRs) that are members of phytochrome-associated, light-sensing two-component signal transduction pathways such as Synechocystis sp. Rcp1, Tolypothrix sp. RcpA, and Agrobacterium tumefaciens bacteriophytochrome response regulator AtBRR. They are stand-alone RRs containing only a REC domain with no output/effector domain. The REC domain itself functions as an effector domain. Also included in this family us Methanosaeta harundinacea methanogenesis regulatory protein FilR2, also a stand-alone RR. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.50165e-63
NZ_CP019636.1\|WP_087543846.1\|6768814_6769915_-\|tocopherol-cyclase	gnl\|CDD\|372979	pfam14249, Tocopherol_cycl, Tocopherol cyclase. This family contains tocopherol cyclases. These enzymes are involved in the synthesis of tocopherols and tocotrienols (vitamin E).	0
NZ_CP019636.1\|WP_087543816.1\|6755655_6756288_+\|NYN-domain-containing-protein	gnl\|CDD\|350235	cd10911, PIN_LabA, PIN domain of Synechococcus elongatus LabA (low-amplitude and bright) and related proteins. This subfamily contains Synechococcus elongatus PCC 7942 LabA which participates in cyanobacterial circadian timing, it is required for negative feedback regulation of the autokinase/autophosphatase KaiC, a central component of the circadian clock system, and appears to be necessary for KaiC-dependent repression of gene expression. This subfamily belongs to the LabA-like domain family which includes the N-terminal domain of limkain b1, a human autoantigen localized to a subset of ABCD3 and PXF marked peroxisomes. Also included in the LabA-like domain family are human ZNF451, uncharacterized Bacillus subtilis YqxD, uncharacterized Escherichia coli YaiI, and the N-terminal domain of a well-conserved group of mainly bacterial proteins with no defined function, which contain a C-terminal LabA_like_C domain. Curiously Pseudomonas putida S16 NicB , which is described as a putative NADH-dependent hydroxylase involved in the microbial degradation of nicotine also falls into the LabA-like family. The PIN (PilT N terminus) domain belongs to a large nuclease superfamily. 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.	3.52095e-70
NZ_CP019636.1\|WP_087543836.1\|6765804_6766842_+\|AI-2E-family-transporter	gnl\|CDD\|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	1.43211e-44
NZ_CP019636.1\|WP_087543824.1\|6761017_6762043_+\|phosphate-acyltransferase-PlsX	gnl\|CDD\|235414	PRK05331, PRK05331, phosphate acyltransferase PlsX.	8.56826e-175
NZ_CP019636.1\|WP_087543838.1\|6766984_6767287_+\|DUF2288-family-protein	gnl\|CDD\|227913	COG5626, COG5626, Uncharacterized small conserved protein [Function unknown].	2.83548e-35
NZ_CP019636.1\|WP_087543812.1\|6753905_6755507_+\|methionine--tRNA-ligase	gnl\|CDD\|237012	PRK11893, PRK11893, methionyl-tRNA synthetase; Reviewed.	0
NZ_CP019636.1\|WP_087543806.1\|6750557_6751784_-\|hypothetical-protein	gnl\|CDD\|226125	COG3597, COG3597, Uncharacterized protein/domain associated with GTPases [Function unknown].	1.52502e-07
NZ_CP019636.1\|WP_087543809.1\|6752801_6753533_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	6.3716e-30
NZ_CP019636.1\|WP_087546412.1\|6751898_6752711_-\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.7176e-15

>NZ_CP019636.1|WP_087543821.1|6758182_6759505_-|D-alanyl-D-alanine-carboxypeptidase
MLALFGSGLISIWLEMAGVNVKPIDALDILAWQGSPGLVFAADPNPAGATTVLEYLKGLQTLKLVAANQTQSQGIWIQSGPILMANHQGTIPLPAASLTKIATSLVALNNFGPDHQFQTLVSATGPLHNGVLHGDLVITGGGDPLFVSEEAIAIGNSLNKMGIKRVEGNLVITGNFAMNFQRNPVLAGQVLKQALHSATWSRGIAFQHSLMPKGTPKPQIVIAGRVKLEAQANPQQTLLLRHHSLPLKQIIKEMNVFSNNEMAQMLADAVGGAQVVQSTAARLARVPQSEIQLINGSGLGQENRISPRAVCAMFMAIQQQALSYQLSLADLFPVSGFDHRGTLHSRHLPPATIMKTGTLRDVSALAGVVPTRDRGLVWFAIINRGTNIGAFRTGQDQLLQRLVQQLQVAPGIPATLAPHLAVNTIPQFGAADRNEMLYGG
>NZ_CP019636.1|WP_087546413.1|6756674_6757931_+|LPS-export-ABC-transporter-periplasmic-protein-LptC
MGEETSERVSSPDGETTPTPSVSVKRRADSVGFATRYLLIPLISLIAIGLVACGGSQTRVTTKPPSESPSPTDKDSNLTFFDVTLEQADEVGRPVWKVRAKQAKYTKEKQIGAAENPYGELYQDGKVVYQVQGQKADIEQDGKQLFLKGQIIATDPRNGMVLRGNELEWRPKEDLLIVRNQLNGTHKQLQAVAQEARVKTREQRMEFSGGVVANSLEPQLQMRTEHLIWQIKEQKLIGDRPVQIDRYKNNQITDRGRGDSAEINLKTKIATVNKNAQIELLDPPAQVASNSMTWNFNSETVTTNSPVRVFHRAEKVAVTANQGEMKIPQKTVYLTGNVYGLGERRQSLKSKTLTWYLDKKLVEAQGDVVYRQVDPPLAFTGQKASGNLQAETIVVTDGGSGNKVVTEIIPQERKAKNQ
>NZ_CP019636.1|WP_087543816.1|6755655_6756288_+|NYN-domain-containing-protein
MLNNLENDSIFTPEQVLENRGRVAIFIDGSNLFYAALQLGIEIDYTKLLCRLTGGSRLLRAFFYTGVDRTNEKQQGFLLWMRRNGYRVIAKDLVQLPDGSKKANLDVEIAVDMMALVDSYDTAVLVSGDGDLAYAVNSVSYRGVRVEVVSLRSMTSDSLINVSDRYIDLEAIKEDIQKTPRQSYPYRPLSAMGFLEDPRESDSQQLEIQE
>NZ_CP019636.1|WP_087543812.1|6753905_6755507_+|methionine--tRNA-ligase
MNQVNKTQKTFALTTPLYYVNDLPHIGSAYTTMAADVVGRFQRLLGHRVLLITGTDEHGQKIQRTAESKGRSPQSFSDEMSAGFVSLWQLLNIQYDRFIRTTSPRHEALVKEFFQKVWESQDIYLGQQKGWYCVSCEEFKEERELLEGHRCPLHPNKEVEWRDEQNYFFRLSKYQEKLQELYKSRPDFIQPESRRNEVLNFVNQGLQDFSISRVNLEWGIPVPVDPNHTIYVWFEALLGYVSALLEPDEEPTLENALAKWWPINLHLIGKDILRFHTVYWPAILMSAGKPLPDRVFVHGFLTKDGQKMGKSLGNTLDPVVLVERYGSDAVRYYFLKEIEFGKDGDFNESRFINVLNADLANDLGNLLNRTLNMVKKYCAGNIPAVTNEEIPLEHSLKAIGLRLGEQVQYAYEALAFNQACETILSLVQASNKFIDEQAPWSLYKQGQQQAVEKVLYAVLESVRLAAYLLSPVIPDISSDIYQQLGFDINFNEQLKTAIAAPFAIHGTWGVLTNQQKLGEPRPIFKRIELPKND
>NZ_CP019636.1|WP_087543809.1|6752801_6753533_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MSVNSPLEISRWLLAALSTKMFRYYEDRIPQDASVLVVSNHRSFMDAPILMATLSSPIRFACHHYMGQVPIMKEIVTGQLGCFPLEEANQQRQQSFFQQSQRLLQSKQIVGVFPEGTKPMVEFTHPNRVGEFQRGFAHLALRAQVQDLAILPIAIASLEEVNTSAVPLRLLSLFDPSEPLFNQPGWHPLVTYRRVAVLIGRPYWIKPLYKEKYQGKKARDVVTQLTNYCHSEIANLLREGCYQ
>NZ_CP019636.1|WP_087546412.1|6751898_6752711_-|alpha/beta-hydrolase
MPKVELKPCFLTPKRLQPELPLLVYLPGMDGTGQLLRSQTAGLEVGFDVRCLAIPREDLTSWDELANNVLDLIHTELEKSSQRPVYLCGESFGGCLAQKVAVKAPQLFKRIILINSASAFHLCPFLDWASQFTYLVPSGLYNIGALALLPFLASLSRISQRDRQELLRSMREVPPKTILWRISLLREFYLEEEKLRRLTQPVLVIAGANDRLLPSVAEAKRLVSIFPKSKMVVLRNSGHACLLETDTNLYKIMKKNNFLEVSAQTAETLG
>NZ_CP019636.1|WP_087543806.1|6750557_6751784_-|hypothetical-protein
MVDKPQQKLKDEEPNNLPAAEEEKPSLLESVAETVGCVFGTAVGVGTAAGNTAIQAGKAVAETAGYVGEATAKQTHKLIEQATHTAGQVTERLSENWLIRRVAGVLNLNWLVSAADNVDLEKAAAAVKKLQQEHPNESPSQIAHRIMVEKATKAGGIGFASSLLPGFAAALLAIDLAATTQLQSEMIYQIAAAYGLDLKDTTRKGEVLAIFGLGLGGGRLLKATGLSLLRNLPFAGAVIGASSNATMIYSLGYAACRFYEAKLDESKSLTSEETLQTLKQQSENYLEKAIAQEAVMDQILVHFILASYPEKTWEEILPQLQALNLSSKSLEVISENIKSPQSLDTLLRQLNRDFAIPLLAQCYKIVRTKGEMTPAAQDIINAIATKFDIDINFVQSTVDASGNFVSKK
>NZ_CP019636.1|WP_157679672.1|6746345_6750308_-|PAS-domain-S-box-protein
MPNFTVTRNVAQVASVFVVVISCVVLIGWMFDIAVLKSVLPGLVTMEVNTAIAFLLSGTSLWLLSRGSSFPVLPRLRVLIAQGLAIAVATFGLLTLCQYLLGWNLGIEKLLFAESPQAVATSHPGRMGANTAVNFLLSGVSLWLLGYKTHRSYWLAQGLSLIVALISLQALIGYAYGVKNFYQFGVYTTSMALHTALAFEVLCLGVLYTHPDRGFMQTITSELNGGAIARMLIPGAIALPFILGWLLLLRHTGQQSDLGSSISLLVIAINVVFLVLIWRNAWFINRVDGERKQVLQMLKQQAATLQEQSELLELTYEAIFVRDAQNAITYWNRSAEEMYGYSKAEAIGQVSHTLLQTQVLQGAQNLDAALLQTGRWQTELIHTRKDGAQIVVESRQVAIHNSEGVLVGFLEVNRDITGRKQVEAALRESEERYRLLAENAPQIVWMTQPDGFVEYFNQRWLDYTGLRPQETLALNWEQVVHPDDLPQALEKWTTGLVTGNSIEVQYRLRRVDGVYRWHIAQALPLRDANDTILKWLGTCTDIDDQKQAEEALRQSEARLRLFVDSDLIGIVIGDVDGGLSEANDAFLHIVGYTRKDFLQGRVRWIDMTPAEYLPLDEAAFLEAQEKGVCTPYEKEYTRKDGSRVPVLIGCAVVGQQKQEAFAQGAVPEVIAFVLDMSERQAALRDRNQAQAERDRFFMLSPDMFCVAGFDSYFKRINPACQRILGYTEAELLAKPFIEFVHAEDRAKTLTEMAKLATGVSTLNFENRYRCQDGSYKWLTWNSVPDVELELVYAVAHDITKRKQTEQTLREQAEALRISRERLDLVIQGAEVGLWYCNLPLDKLIWNDQCKAHFGLPPDAEVTIDLFYQLLHPDDREPTQQAIESSIAQTGGYDVDYRTVAPDGRIRWIRAIGNTFCDADGIPKRFDGITIDISDRKRAEAALIESEQRFRYVTDTAPMMVWMAGTDKLCHYFNKPWLDFTGRTRSQELGNGWAEGVHPDDLQRCLETYVNAFDTRQDFQMEYRLRRFDGEYRWVLNIGVSRYTPEGEFIGYIGSCIDIEDRKQVEAQIRQINETLEERVKQRTVQLEAANKELESFSYSVSHDLRAPLRHITGFVDLLQKRLQSTVLDDTTQRYLNIITEATKQAGKLIDDLLTFSRVGRSEMRHTTIDMNLLLHEVQRDLVPETKNRQVSWEIESLAHVHGDPSMLRLVLRNLLENALKYSKTRHITQITVGSVSSHQEVVFFVRDNGIGFDMKYVHKLFGVFQRLHSDPQFEGTGVGLANVQRIIHRHGGRVWAEGEIDNGATFYFSLPRGSGVESGE
>NZ_CP019636.1|WP_087543803.1|6745858_6746335_-|response-regulator
MELKRILLVEDSINDVELILTSLAENHLGNEVVVVRDGEEALDYLYRRGLYRLRREGNPVVVLLDLKLPKVDGIEVLMHLKADPELRVVPVVVLTSSREEQDLARCYELGTNAYVVKPIDFHEFVDVIKGLGLFWAIINEPPPGSIPPARSSQGVAGI
>NZ_CP019636.1|WP_087543800.1|6741774_6743253_-|leucyl-aminopeptidase
MEIRTTDTPLLEWTGDGLAIGLFEDAVELTGELASLDEKLAGSIKELITEEEFKGKQGSSAVTRVGTHSPVRKIILVGLGKPEALKLETLRKAAASAGRLGKKQKCKTLGISLPTWNNDPTQTAQAIAEGVQLALYQDNRFKSEPEDKGPQVEQIDLLGLGGQEAAITRAHQIASGVFLARQLVAAPANSVTPITMAETAQAIASEHGLQIEILEQEECEKLGMGAFLGVAKASDLPPKFIHLTYKPEGTPKRKVAIIGKGLTFDSGGLNIKGAGSGIETMKIDMGGSAATLGAAKAIGQLKPDVEVHFISAVTENMISGRAMHPGDILTASNGKTIEVNNTDAEGRLTLADALVFAEKLGVDAIVDLATLTGACVIALGDDIAGLFSPDDALAEQLEKASEASGEKIWRLPMEEKYFEGLKSGIADMKNTGPRPGGSITAALFLKQFVKDTAWAHLDIAGPVWADKENGYNGPGATGFGVRTLVNWVLSDS
>NZ_CP019636.1|WP_087543824.1|6761017_6762043_+|phosphate-acyltransferase-PlsX
MGSTCARIAIDAMGGDHAPGEIVAGALRAREELGVEVLLVGDPQQIESKLPPKINLGQVEIVPAEEAIAMDEEPLSGIRRKPKASINVAMDLVKRQQADAVVSAGHSGAAMAAALLRLGRLKGIDRPAIGAVFPTMVAGKPVLILDVGANVDCRPKFLEQFAIMGSVYSQYVLGVEQPLVGLLNIGEEDSKGNDAAVRAHQLLRENRQIKFIGNAEGRDVLSGHFDVIVCDGFVGNVLLKFAEAVGEIMLQILREELPQGLHGQIGTAILKPNLKRIKQRMDHAEHGGALLLGVDGICIISHGSSQAPSVFNAIRMAKEAVDHQVLNRIQFQYQSIQRESG
>NZ_CP019636.1|WP_087543827.1|6762155_6763148_+|beta-ketoacyl-ACP-synthase-III
MQNLGIAITGSGSAVPTTFLDNQALTELVETSDEWVTTRTGIRQRRLAKPSETITDLATNASRQAIAMAGINPQELDLILLATSTPDDLFGSACQIQAQLGATTAVAFDLTAACSGFVFGLVTAAQYIRTGVYRNVLLIGADILSRWVDWQDRRTCVLFGDGAGAVVIQANEKDCLLGFELRSDGTQNNCLNLAYAFEPRELTQGVNVGKGNFQPITMNGKEVYRFAVQKVPEVIDKALFRANLTIDQIDWLLLHQANQRILDAVAQRLNIPEHKVISHLANYGNTSAASIPLALDATVRQGKIKTGDIIATSGFGAGLTWGAAIFQWGR
>NZ_CP019636.1|WP_157679673.1|6763222_6763393_+|hypothetical-protein
MPLDGRCYKSDIARPTHCLLYAGEPFRQSLMGGTPKTALPHHRSGSPPVALAPFDS
>NZ_CP019636.1|WP_087543830.1|6763430_6764309_+|ACP-S-malonyltransferase
MTKTAWVFPGQGSQSQGMGIDLLDVPSAKEKFAQAEDILGWSVIGICQNNAEKLSHTLYTQPCLYVVESILADILREKEQPNLVAGHSLGEYVALYVAGVFDWSAGLRLVKRRAELMESTAGGMMAALMNFNREQLEKVIAETPDVVVANDNSPAQVVISGTPAAVEFVLSQVKAKRAKPLNVSGAFHSPLMAAAAAEFQDILESVEFQQAFVPVLSNVEPVPSVDATVLKQRLMQQMTGGVRWREISLALPEHGIERVVEIGPGNVLTGLIKRICSNLILENVSNLATLEK
>NZ_CP019636.1|WP_087543833.1|6764774_6765413_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MSRSREPYASLLLYHTFKWSVVSPLLHVYFQGRIYGAENVPPTGPLVVVSNHASNYDPPIVSNCVRRPVAYMAKEELFKIPVFSKAIQLYGAYPVSRGSSDRTAIRAAMKYLDDGWAVGIFLQGTRTPDGRITDPKRGAALIAAKAKVPLLPVCLWGTQAIEQKGSITPRPVPVTVRIGNLIDAPSSSNKEELEALTQKCAAEINALHDLGR
>NZ_CP019636.1|WP_157679729.1|6765640_6765727_+|hypothetical-protein
MWIITNNYLKNGRFFVFNSQEKYHKTRI
>NZ_CP019636.1|WP_087543836.1|6765804_6766842_+|AI-2E-family-transporter
MSGFDANNLWYRLNNLALVRFLLLVASGWAIVLLLDYFESVIVIFTFAAILAFLLSYPVQWLRHFLPHGVSVVVIFLLSIVILGGLAITVGLTILSQGQQLIDSVTAFLNSLIPFVERIEEFLRNRNLPIDLSAIEEQLRNRAITLLVTSLNIFQSFITNFVTFILIAVVAFFMLLDGEKLWHFVLRIVPQRRRDRFTKIIKRNFLGFFRGQLILTLFLTCTTFIVFLVMKVPFPLILSIIVGVIDIIPGIGATLGVSVITLIVLSQSVWMAIKVLVACIILQQIQDNLIAPRIMQGALNLNPVVVFFALLVGARVAGLLGIFISIPITGVLVSLFEIDAMKSEV
>NZ_CP019636.1|WP_087543838.1|6766984_6767287_+|DUF2288-family-protein
MTNTDLRAELTENLDEAEWEWLIPHARRDAVIVVAEELDLLDVGLAIASDNASEVQIWIDEALITKPSVEQIGEWNNQPTKRFHTLIIQPYVLVQEKAAA
>NZ_CP019636.1|WP_087543840.1|6767515_6768046_-|YdcF-family-protein
MFLALPLMMLWGYKEIQSQFVKPQAILVLGGSTSKLEREKFTADFAHQHPNIPIWISGGSPPKATKRVFAKAGVDTKRLRLDYRANNTVENFTTIVDDLKKSGVKSVYLVTSDYHMRRARIIGEIVLGSRGIDFRPVAVPSQTSSEPIEKSIRDGVRAIVWVATGFADADEFQNKQ
>NZ_CP019636.1|WP_087543846.1|6768814_6769915_-|tocopherol-cyclase
MLTISTNSHLSTQTPHSGYHWDGSSRRFFEGWYYRVTLPAEGQTFAFMYSIEDPVGNKPHSGGAAQILGPNDEYLWRTFPDVSKFWASREILGLGHWGKTDLQHSKPLYLPPPEFERHVQEGYQATATLNQGAIHDPATGHYCRWQYEIHPIYGWGDKGSIQQSTAGWLSFLQIFEPGWQILMAHGLASGWIDWNGKLYEFTNVPAYSEKNWGGAFPQKWFWLNCNTFEGESDLALTAGGGRRGVLWWMESVAMIGVHHQGKFYEFVPWNSEVHWDIQPWGKWQMQARNSHYEIEVTGTTDLPGTPLRAPTAKGLLFCCRDTMQGQLNLELRELGVGKRKIILKAQSFLCGLEIGGGPWDTSWQSR

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Crispr_ID: NZ_CP019636_23

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_23

6764555-6764664

Orphan

Consensus_repeat	Method
TCACCAGACGCACTCGCGTTCGGGT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_23

>merge|NZ_CP019636|23|6764555-6764664|CRISPRCasFinder
TCACCAGACGCACTCGCGTTCGGGTGAATCCTGCGGATACGCTCCGCGAGCGCCAGTTCCCTACGGAGGGAAACCCCTTCTCTTGTCACCAGACGCACTCGCGTTCGGGT

>NZ_CP019636|23|22|6764555-6764664|CRISPRCasFinder
TCACCAGACGCACTCGCGTTCGGGT	GAATCCTGCGGATACGCTCCGCGAGCGCCAGTTCCCTACGGAGGGAAACCCCTTCTCTTG
TCACCAGACGCACTCGCGTTCGGGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_157679673.1\|6763222_6763393_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543827.1\|6762155_6763148_+\|beta-ketoacyl-ACP-synthase-III	unknown	unknown	gnl\|CDD\|236475
NZ_CP019636.1\|WP_087543854.1\|6774387_6775530_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|349760
NZ_CP019636.1\|WP_087543840.1\|6767515_6768046_-\|YdcF-family-protein	unknown	unknown	gnl\|CDD\|99750
NZ_CP019636.1\|WP_087543821.1\|6758182_6759505_-\|D-alanyl-D-alanine-carboxypeptidase	unknown	unknown	gnl\|CDD\|224938
NZ_CP019636.1\|WP_087543848.1\|6769944_6770559_+\|DnaJ-domain-containing-protein	unknown	unknown	gnl\|CDD\|223560
NZ_CP019636.1\|WP_087543809.1\|6752801_6753533_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP019636.1\|WP_087546413.1\|6756674_6757931_+\|LPS-export-ABC-transporter-periplasmic-protein-LptC	unknown	unknown	gnl\|CDD\|275202
NZ_CP019636.1\|WP_087543830.1\|6763430_6764309_+\|ACP-S-malonyltransferase	unknown	unknown	gnl\|CDD\|223408
NZ_CP019636.1\|WP_087543846.1\|6768814_6769915_-\|tocopherol-cyclase	unknown	unknown	gnl\|CDD\|372979
NZ_CP019636.1\|WP_087543816.1\|6755655_6756288_+\|NYN-domain-containing-protein	unknown	unknown	gnl\|CDD\|350235
NZ_CP019636.1\|WP_157679729.1\|6765640_6765727_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087543851.1\|6773370_6774204_-\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|224326
NZ_CP019636.1\|WP_087543824.1\|6761017_6762043_+\|phosphate-acyltransferase-PlsX	unknown	unknown	gnl\|CDD\|235414
NZ_CP019636.1\|WP_087543838.1\|6766984_6767287_+\|DUF2288-family-protein	unknown	unknown	gnl\|CDD\|227913
NZ_CP019636.1\|WP_087543812.1\|6753905_6755507_+\|methionine--tRNA-ligase	unknown	unknown	gnl\|CDD\|237012
NZ_CP019636.1\|WP_087543836.1\|6765804_6766842_+\|AI-2E-family-transporter	unknown	unknown	gnl\|CDD\|223701
NZ_CP019636.1\|WP_087543833.1\|6764774_6765413_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP019636.1\|WP_087546414.1\|6770731_6772789_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238121
NZ_CP019636.1\|WP_087546412.1\|6751898_6752711_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087543821.1\|6758182_6759505_-\|D-alanyl-D-alanine-carboxypeptidase	gnl\|CDD\|224938	COG2027, DacB, D-alanyl-D-alanine carboxypeptidase (penicillin-binding protein 4) [Cell envelope biogenesis, outer membrane].	3.00124e-64
NZ_CP019636.1\|WP_087543827.1\|6762155_6763148_+\|beta-ketoacyl-ACP-synthase-III	gnl\|CDD\|236475	PRK09352, PRK09352, beta-ketoacyl-ACP synthase 3.	1.06342e-178
NZ_CP019636.1\|WP_087543854.1\|6774387_6775530_+\|AAA-family-ATPase	gnl\|CDD\|349760	cd02042, ParAB_family, partition proteins ParAB family. ParA and ParB of Caulobacter crescentus belong to a conserved family of bacterial proteins implicated in chromosome segregation. ParB binds to DNA sequences adjacent to the origin of replication and localizes to opposite cell poles shortly following the initiation of DNA replication. ParB regulates the ParA ATPase activity by promoting nucleotide exchange in a fashion reminiscent of the exchange factors of eukaryotic G proteins. ADP-bound ParA binds single-stranded DNA, whereas the ATP-bound form dissociates ParB from its DNA binding sites. Increasing the fraction of ParA-ADP in the cell inhibits cell division, suggesting that this simple nucleotide switch may regulate cytokinesis. ParA shares sequence similarity to a conserved and widespread family of ATPases which includes the repA protein of the repABC operon in Rhizobium etli symbiotic plasmid. This operon is involved in the plasmid replication and partition.	2.03528e-17
NZ_CP019636.1\|WP_087543840.1\|6767515_6768046_-\|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.	1.12061e-27
NZ_CP019636.1\|WP_087543830.1\|6763430_6764309_+\|ACP-S-malonyltransferase	gnl\|CDD\|223408	COG0331, FabD, (acyl-carrier-protein) S-malonyltransferase [Lipid metabolism].	2.56501e-107
NZ_CP019636.1\|WP_087543851.1\|6773370_6774204_-\|metallophosphoesterase	gnl\|CDD\|224326	COG1408, COG1408, Predicted phosphohydrolases [General function prediction only].	1.02668e-71
NZ_CP019636.1\|WP_087543809.1\|6752801_6753533_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	6.3716e-30
NZ_CP019636.1\|WP_087546413.1\|6756674_6757931_+\|LPS-export-ABC-transporter-periplasmic-protein-LptC	gnl\|CDD\|275202	TIGR04409, LptC_YrbK, LPS export ABC transporter periplasmic protein LptC. Members of this family are LptC, a periplasmic protein tethered to the inner membrane in the lipopolysaccharide (LPS)exporter transenvelope complex (Lpt), which is responsible for conducting LPS to the outer leaflet of the outer membrane in most Gram-negative bacteria. LptC is homologous to LptA, another member of the transenvelope complex. Genes lptC and lptA are often adjacent. [Cell envelope, Biosynthesis and degradation of surface polysaccharides and lipopolysaccharides, Transport and binding proteins, Other].	1.38767e-11
NZ_CP019636.1\|WP_087543848.1\|6769944_6770559_+\|DnaJ-domain-containing-protein	gnl\|CDD\|223560	COG0484, DnaJ, DnaJ-class molecular chaperone with C-terminal Zn finger domain [Posttranslational modification, protein turnover, chaperones].	4.04834e-17
NZ_CP019636.1\|WP_087543846.1\|6768814_6769915_-\|tocopherol-cyclase	gnl\|CDD\|372979	pfam14249, Tocopherol_cycl, Tocopherol cyclase. This family contains tocopherol cyclases. These enzymes are involved in the synthesis of tocopherols and tocotrienols (vitamin E).	0
NZ_CP019636.1\|WP_087543816.1\|6755655_6756288_+\|NYN-domain-containing-protein	gnl\|CDD\|350235	cd10911, PIN_LabA, PIN domain of Synechococcus elongatus LabA (low-amplitude and bright) and related proteins. This subfamily contains Synechococcus elongatus PCC 7942 LabA which participates in cyanobacterial circadian timing, it is required for negative feedback regulation of the autokinase/autophosphatase KaiC, a central component of the circadian clock system, and appears to be necessary for KaiC-dependent repression of gene expression. This subfamily belongs to the LabA-like domain family which includes the N-terminal domain of limkain b1, a human autoantigen localized to a subset of ABCD3 and PXF marked peroxisomes. Also included in the LabA-like domain family are human ZNF451, uncharacterized Bacillus subtilis YqxD, uncharacterized Escherichia coli YaiI, and the N-terminal domain of a well-conserved group of mainly bacterial proteins with no defined function, which contain a C-terminal LabA_like_C domain. Curiously Pseudomonas putida S16 NicB , which is described as a putative NADH-dependent hydroxylase involved in the microbial degradation of nicotine also falls into the LabA-like family. The PIN (PilT N terminus) domain belongs to a large nuclease superfamily. 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.	3.52095e-70
NZ_CP019636.1\|WP_087543836.1\|6765804_6766842_+\|AI-2E-family-transporter	gnl\|CDD\|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	1.43211e-44
NZ_CP019636.1\|WP_087543824.1\|6761017_6762043_+\|phosphate-acyltransferase-PlsX	gnl\|CDD\|235414	PRK05331, PRK05331, phosphate acyltransferase PlsX.	8.56826e-175
NZ_CP019636.1\|WP_087543838.1\|6766984_6767287_+\|DUF2288-family-protein	gnl\|CDD\|227913	COG5626, COG5626, Uncharacterized small conserved protein [Function unknown].	2.83548e-35
NZ_CP019636.1\|WP_087543812.1\|6753905_6755507_+\|methionine--tRNA-ligase	gnl\|CDD\|237012	PRK11893, PRK11893, methionyl-tRNA synthetase; Reviewed.	0
NZ_CP019636.1\|WP_087543833.1\|6764774_6765413_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	1.10167e-55
NZ_CP019636.1\|WP_087546414.1\|6770731_6772789_+\|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.	4.51986e-104
NZ_CP019636.1\|WP_087546412.1\|6751898_6752711_-\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.7176e-15

>NZ_CP019636.1|WP_087543830.1|6763430_6764309_+|ACP-S-malonyltransferase
MTKTAWVFPGQGSQSQGMGIDLLDVPSAKEKFAQAEDILGWSVIGICQNNAEKLSHTLYTQPCLYVVESILADILREKEQPNLVAGHSLGEYVALYVAGVFDWSAGLRLVKRRAELMESTAGGMMAALMNFNREQLEKVIAETPDVVVANDNSPAQVVISGTPAAVEFVLSQVKAKRAKPLNVSGAFHSPLMAAAAAEFQDILESVEFQQAFVPVLSNVEPVPSVDATVLKQRLMQQMTGGVRWREISLALPEHGIERVVEIGPGNVLTGLIKRICSNLILENVSNLATLEK
>NZ_CP019636.1|WP_157679673.1|6763222_6763393_+|hypothetical-protein
MPLDGRCYKSDIARPTHCLLYAGEPFRQSLMGGTPKTALPHHRSGSPPVALAPFDS
>NZ_CP019636.1|WP_087543827.1|6762155_6763148_+|beta-ketoacyl-ACP-synthase-III
MQNLGIAITGSGSAVPTTFLDNQALTELVETSDEWVTTRTGIRQRRLAKPSETITDLATNASRQAIAMAGINPQELDLILLATSTPDDLFGSACQIQAQLGATTAVAFDLTAACSGFVFGLVTAAQYIRTGVYRNVLLIGADILSRWVDWQDRRTCVLFGDGAGAVVIQANEKDCLLGFELRSDGTQNNCLNLAYAFEPRELTQGVNVGKGNFQPITMNGKEVYRFAVQKVPEVIDKALFRANLTIDQIDWLLLHQANQRILDAVAQRLNIPEHKVISHLANYGNTSAASIPLALDATVRQGKIKTGDIIATSGFGAGLTWGAAIFQWGR
>NZ_CP019636.1|WP_087543824.1|6761017_6762043_+|phosphate-acyltransferase-PlsX
MGSTCARIAIDAMGGDHAPGEIVAGALRAREELGVEVLLVGDPQQIESKLPPKINLGQVEIVPAEEAIAMDEEPLSGIRRKPKASINVAMDLVKRQQADAVVSAGHSGAAMAAALLRLGRLKGIDRPAIGAVFPTMVAGKPVLILDVGANVDCRPKFLEQFAIMGSVYSQYVLGVEQPLVGLLNIGEEDSKGNDAAVRAHQLLRENRQIKFIGNAEGRDVLSGHFDVIVCDGFVGNVLLKFAEAVGEIMLQILREELPQGLHGQIGTAILKPNLKRIKQRMDHAEHGGALLLGVDGICIISHGSSQAPSVFNAIRMAKEAVDHQVLNRIQFQYQSIQRESG
>NZ_CP019636.1|WP_087543821.1|6758182_6759505_-|D-alanyl-D-alanine-carboxypeptidase
MLALFGSGLISIWLEMAGVNVKPIDALDILAWQGSPGLVFAADPNPAGATTVLEYLKGLQTLKLVAANQTQSQGIWIQSGPILMANHQGTIPLPAASLTKIATSLVALNNFGPDHQFQTLVSATGPLHNGVLHGDLVITGGGDPLFVSEEAIAIGNSLNKMGIKRVEGNLVITGNFAMNFQRNPVLAGQVLKQALHSATWSRGIAFQHSLMPKGTPKPQIVIAGRVKLEAQANPQQTLLLRHHSLPLKQIIKEMNVFSNNEMAQMLADAVGGAQVVQSTAARLARVPQSEIQLINGSGLGQENRISPRAVCAMFMAIQQQALSYQLSLADLFPVSGFDHRGTLHSRHLPPATIMKTGTLRDVSALAGVVPTRDRGLVWFAIINRGTNIGAFRTGQDQLLQRLVQQLQVAPGIPATLAPHLAVNTIPQFGAADRNEMLYGG
>NZ_CP019636.1|WP_087546413.1|6756674_6757931_+|LPS-export-ABC-transporter-periplasmic-protein-LptC
MGEETSERVSSPDGETTPTPSVSVKRRADSVGFATRYLLIPLISLIAIGLVACGGSQTRVTTKPPSESPSPTDKDSNLTFFDVTLEQADEVGRPVWKVRAKQAKYTKEKQIGAAENPYGELYQDGKVVYQVQGQKADIEQDGKQLFLKGQIIATDPRNGMVLRGNELEWRPKEDLLIVRNQLNGTHKQLQAVAQEARVKTREQRMEFSGGVVANSLEPQLQMRTEHLIWQIKEQKLIGDRPVQIDRYKNNQITDRGRGDSAEINLKTKIATVNKNAQIELLDPPAQVASNSMTWNFNSETVTTNSPVRVFHRAEKVAVTANQGEMKIPQKTVYLTGNVYGLGERRQSLKSKTLTWYLDKKLVEAQGDVVYRQVDPPLAFTGQKASGNLQAETIVVTDGGSGNKVVTEIIPQERKAKNQ
>NZ_CP019636.1|WP_087543816.1|6755655_6756288_+|NYN-domain-containing-protein
MLNNLENDSIFTPEQVLENRGRVAIFIDGSNLFYAALQLGIEIDYTKLLCRLTGGSRLLRAFFYTGVDRTNEKQQGFLLWMRRNGYRVIAKDLVQLPDGSKKANLDVEIAVDMMALVDSYDTAVLVSGDGDLAYAVNSVSYRGVRVEVVSLRSMTSDSLINVSDRYIDLEAIKEDIQKTPRQSYPYRPLSAMGFLEDPRESDSQQLEIQE
>NZ_CP019636.1|WP_087543812.1|6753905_6755507_+|methionine--tRNA-ligase
MNQVNKTQKTFALTTPLYYVNDLPHIGSAYTTMAADVVGRFQRLLGHRVLLITGTDEHGQKIQRTAESKGRSPQSFSDEMSAGFVSLWQLLNIQYDRFIRTTSPRHEALVKEFFQKVWESQDIYLGQQKGWYCVSCEEFKEERELLEGHRCPLHPNKEVEWRDEQNYFFRLSKYQEKLQELYKSRPDFIQPESRRNEVLNFVNQGLQDFSISRVNLEWGIPVPVDPNHTIYVWFEALLGYVSALLEPDEEPTLENALAKWWPINLHLIGKDILRFHTVYWPAILMSAGKPLPDRVFVHGFLTKDGQKMGKSLGNTLDPVVLVERYGSDAVRYYFLKEIEFGKDGDFNESRFINVLNADLANDLGNLLNRTLNMVKKYCAGNIPAVTNEEIPLEHSLKAIGLRLGEQVQYAYEALAFNQACETILSLVQASNKFIDEQAPWSLYKQGQQQAVEKVLYAVLESVRLAAYLLSPVIPDISSDIYQQLGFDINFNEQLKTAIAAPFAIHGTWGVLTNQQKLGEPRPIFKRIELPKND
>NZ_CP019636.1|WP_087543809.1|6752801_6753533_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MSVNSPLEISRWLLAALSTKMFRYYEDRIPQDASVLVVSNHRSFMDAPILMATLSSPIRFACHHYMGQVPIMKEIVTGQLGCFPLEEANQQRQQSFFQQSQRLLQSKQIVGVFPEGTKPMVEFTHPNRVGEFQRGFAHLALRAQVQDLAILPIAIASLEEVNTSAVPLRLLSLFDPSEPLFNQPGWHPLVTYRRVAVLIGRPYWIKPLYKEKYQGKKARDVVTQLTNYCHSEIANLLREGCYQ
>NZ_CP019636.1|WP_087546412.1|6751898_6752711_-|alpha/beta-hydrolase
MPKVELKPCFLTPKRLQPELPLLVYLPGMDGTGQLLRSQTAGLEVGFDVRCLAIPREDLTSWDELANNVLDLIHTELEKSSQRPVYLCGESFGGCLAQKVAVKAPQLFKRIILINSASAFHLCPFLDWASQFTYLVPSGLYNIGALALLPFLASLSRISQRDRQELLRSMREVPPKTILWRISLLREFYLEEEKLRRLTQPVLVIAGANDRLLPSVAEAKRLVSIFPKSKMVVLRNSGHACLLETDTNLYKIMKKNNFLEVSAQTAETLG
>NZ_CP019636.1|WP_087543833.1|6764774_6765413_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MSRSREPYASLLLYHTFKWSVVSPLLHVYFQGRIYGAENVPPTGPLVVVSNHASNYDPPIVSNCVRRPVAYMAKEELFKIPVFSKAIQLYGAYPVSRGSSDRTAIRAAMKYLDDGWAVGIFLQGTRTPDGRITDPKRGAALIAAKAKVPLLPVCLWGTQAIEQKGSITPRPVPVTVRIGNLIDAPSSSNKEELEALTQKCAAEINALHDLGR
>NZ_CP019636.1|WP_157679729.1|6765640_6765727_+|hypothetical-protein
MWIITNNYLKNGRFFVFNSQEKYHKTRI
>NZ_CP019636.1|WP_087543836.1|6765804_6766842_+|AI-2E-family-transporter
MSGFDANNLWYRLNNLALVRFLLLVASGWAIVLLLDYFESVIVIFTFAAILAFLLSYPVQWLRHFLPHGVSVVVIFLLSIVILGGLAITVGLTILSQGQQLIDSVTAFLNSLIPFVERIEEFLRNRNLPIDLSAIEEQLRNRAITLLVTSLNIFQSFITNFVTFILIAVVAFFMLLDGEKLWHFVLRIVPQRRRDRFTKIIKRNFLGFFRGQLILTLFLTCTTFIVFLVMKVPFPLILSIIVGVIDIIPGIGATLGVSVITLIVLSQSVWMAIKVLVACIILQQIQDNLIAPRIMQGALNLNPVVVFFALLVGARVAGLLGIFISIPITGVLVSLFEIDAMKSEV
>NZ_CP019636.1|WP_087543838.1|6766984_6767287_+|DUF2288-family-protein
MTNTDLRAELTENLDEAEWEWLIPHARRDAVIVVAEELDLLDVGLAIASDNASEVQIWIDEALITKPSVEQIGEWNNQPTKRFHTLIIQPYVLVQEKAAA
>NZ_CP019636.1|WP_087543840.1|6767515_6768046_-|YdcF-family-protein
MFLALPLMMLWGYKEIQSQFVKPQAILVLGGSTSKLEREKFTADFAHQHPNIPIWISGGSPPKATKRVFAKAGVDTKRLRLDYRANNTVENFTTIVDDLKKSGVKSVYLVTSDYHMRRARIIGEIVLGSRGIDFRPVAVPSQTSSEPIEKSIRDGVRAIVWVATGFADADEFQNKQ
>NZ_CP019636.1|WP_087543846.1|6768814_6769915_-|tocopherol-cyclase
MLTISTNSHLSTQTPHSGYHWDGSSRRFFEGWYYRVTLPAEGQTFAFMYSIEDPVGNKPHSGGAAQILGPNDEYLWRTFPDVSKFWASREILGLGHWGKTDLQHSKPLYLPPPEFERHVQEGYQATATLNQGAIHDPATGHYCRWQYEIHPIYGWGDKGSIQQSTAGWLSFLQIFEPGWQILMAHGLASGWIDWNGKLYEFTNVPAYSEKNWGGAFPQKWFWLNCNTFEGESDLALTAGGGRRGVLWWMESVAMIGVHHQGKFYEFVPWNSEVHWDIQPWGKWQMQARNSHYEIEVTGTTDLPGTPLRAPTAKGLLFCCRDTMQGQLNLELRELGVGKRKIILKAQSFLCGLEIGGGPWDTSWQSR
>NZ_CP019636.1|WP_087543848.1|6769944_6770559_+|DnaJ-domain-containing-protein
MSDRLNINDAYSILGLEPGALPAEVKQAYRKLVKIWHPDRFPHPQKKQEAEEKIKQINEAYNKLKSYLLTSANQPSQTKQTKEPNIYANRSNAELFYNWGAENAKLGRYEEALADFTHAIRLNPNYIEAYKYRGFICSLLGYEHRATADLNKAELMEGKLKNKQGHSASSPRYSTTSRRKSKLRSFLERFLQWIRSLLGFDRRF
>NZ_CP019636.1|WP_087546414.1|6770731_6772789_+|hypothetical-protein
MTKLHWLEVTEYASLSLSALGLVTAAVTQQMIYAAAPLTMTVCLNVANRERLKSLTQQDQQATIAKMDLLIDPLRQRLANFDTFTHKLSATTERQLEDLKINQQQDVNIFTERFQELDTSLLAVTTRIQQQIQELQQNQQEQSLTQLDTLMQQLSTSTQQQIDPLYQRLAQIDTFIQQLSQTTQQQIQSLQRNQQEQNIETLSQRLTQLDTLTQQLSTKAQQIDPLYQRLSQLDSFAQQLNQYTQHQVQVLQRTQQEQNVEILRQNLTQLDAFTQNLSINTQKQIQEFHYAIALIQAELQELSQLKQQYQNLPESKKKPEGSDPPQPPITTKSPTSILQNEQPPNSPPRLSPITAIQSPNSQVNKTTNTASVPVVTAPTLAPIIEGLPVETPVAHKVTSVAFSPNGQVVASGCDDKTIKIWHLDNNEPRLLKENREFSCDGGVNSLAFSPDGKILASGCDDKTIRLWDISTGNETCTFTGHREKVTSVAFSPDGKTLASGSRDKTIKLWSIDTNKETSTLHGHCDEVLCVTFNPDGKILASGGAKKDKTIKVWYLAENKFLTLKGHSDELGGIHSIAFSPDGETLASGSTDKTIRIWQLSSGQEIHTLTGHSDDVYSVTFSPDGKTLASASKDKTVKLWQVDTGLETRTFTESEEPIYCVAFSPDGRTLVAGGHGENTVMLLPCD
>NZ_CP019636.1|WP_087543851.1|6773370_6774204_-|metallophosphoesterase
MHWLLSGPLSVEKLTVSIAGLPASLQGTKLVHMSDLHYDGKRLSEEMLEEAIAVSNEAEPDLVVLTGDYVTDDPSPIHQLVLRLKHLQSRAGIYAVLGNHDLHYSRSKAEVTAALNSIDIKVLWNEIAYPLGKELPVVGLADYWSREFHPQAVMNQLDGSVPCIVLSHNPDTAEILQKWRVDLQLSGHTHGGQIVLPGIGPVVIYYKQFVRQLPRKLRRWVPFLRGDCSKVVKHWEWAQGFHKVGTNQLYINRGLGTYSPGRLFCPPEVTVMTLTSQ
>NZ_CP019636.1|WP_087543854.1|6774387_6775530_+|AAA-family-ATPase
MEPVYTKDYSHFKQHVAKLLHRAGWTVITVNSNQPGYDLVVKKGSLVGAVAIKWLRNNVAAPQLLKFSNFLDSDEGKKFNFGLFITTKGYSGPALALIRSWGKDTKIRCGIAKENTLAGIDSADYEDRANDDSTRPEKVYFGIFTCKGGVGKTTIAGHLAGAFALQGFNVALVDLDPEQNLQKLVGDGVFVPNSRGRGTTIEVFDGRDWHEDSARDCKIVICDCSPALERNPTNLIEKFHYCLIPTTLNPLGINKHGKVIRDTVTEIRAINKNAHLFVLVNNFKNPGSQKLRLLRKVYFDTYKDIIKTDEKFHCIDPKEVCIRASEQLYYWGIHILENPENPSSRLAFDLIGGKSYPREDFISLADYIERKAGIGVLRDQ

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Crispr_ID: NZ_CP019636_24

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_24

7250382-7250507

Orphan

Consensus_repeat	Method
CGCTAACGCCAGTTGCCGTGAGAGCGGGAAACCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_24

>merge|NZ_CP019636|24|7250382-7250507|CRISPRCasFinder
CGCTAACGCCAGTTGCCGTGAGAGCGGGAAACCCCTTCGGGTAACGCTCCTTTGTCGCTACCGCTTCTCCTATCACCAGACGCACTCGCGTTCGCTAACGCCAATTGCCGTGAGAGCGGGAAACCC

>NZ_CP019636|24|23|7250382-7250507|CRISPRCasFinder
CGCTAACGCCAGTTGCCGTGAGAGCGGGAAACCC	CTTCGGGTAACGCTCCTTTGTCGCTACCGCTTCTCCTATCACCAGACGCACTCGCGTT
CGCTAACGCCAATTGCCGTGAGAGCGGGAAACCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087544681.1\|7250707_7252702_-\|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl\|CDD\|119407
NZ_CP019636.1\|WP_157679688.1\|7255759_7255948_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087544697.1\|7260844_7261852_+\|rod-shape-determining-protein	unknown	unknown	gnl\|CDD\|237562
NZ_CP019636.1\|WP_087544695.1\|7260109_7260472_-\|single-stranded-DNA-binding-protein	unknown	unknown	gnl\|CDD\|180986
NZ_CP019636.1\|WP_157679689.1\|7256361_7256691_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087544675.1\|7246993_7247965_-\|solanesyl-diphosphate-synthase	unknown	unknown	gnl\|CDD\|131796
NZ_CP019636.1\|WP_087544671.1\|7244911_7246102_-\|heterocyst-differentiation-protein-HetZ	unknown	unknown	unknown
NZ_CP019636.1\|WP_087544691.1\|7258431_7258845_-\|EVE-domain-containing-protein	unknown	unknown	gnl\|CDD\|376640
NZ_CP019636.1\|WP_087544685.1\|7253558_7255499_-\|N-acetylmuramoyl-L-alanine-amidase	unknown	unknown	gnl\|CDD\|119407
NZ_CP019636.1\|WP_087544689.1\|7256918_7258346_-\|cation:proton-antiporter	unknown	unknown	gnl\|CDD\|223551
NZ_CP019636.1\|WP_087538477.1\|7240326_7241238_-\|IS982-family-transposase	unknown	unknown	gnl\|CDD\|372648
NZ_CP019636.1\|WP_087544665.1\|7239344_7239614_-\|DUF370-domain-containing-protein	unknown	unknown	gnl\|CDD\|179823
NZ_CP019636.1\|WP_087544677.1\|7248986_7249184_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087544679.1\|7249251_7250112_-\|glutamate-racemase	unknown	unknown	gnl\|CDD\|234851
NZ_CP019636.1\|WP_087544693.1\|7259292_7260045_+\|DUF541-domain-containing-protein	unknown	unknown	gnl\|CDD\|225516
NZ_CP019636.1\|WP_157679687.1\|7252830_7253076_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087544673.1\|7246306_7246780_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087544667.1\|7241381_7243709_-\|DUF3488-domain-containing-protein	unknown	unknown	gnl\|CDD\|224224
NZ_CP019636.1\|WP_087544663.1\|7238576_7239179_-\|guanylate-kinase	unknown	unknown	gnl\|CDD\|234719
NZ_CP019636.1\|WP_087544669.1\|7243938_7244919_-\|PatU	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087544681.1\|7250707_7252702_-\|N-acetylmuramoyl-L-alanine-amidase	gnl\|CDD\|119407	cd02696, MurNAc-LAA, N-acetylmuramoyl-L-alanine amidase or MurNAc-LAA (also known as peptidoglycan aminohydrolase, NAMLA amidase, NAMLAA, Amidase 3, and peptidoglycan amidase; EC 3.5.1.28) is an autolysin that hydrolyzes the amide bond between N-acetylmuramoyl and L-amino acids in certain cell wall glycopeptides. These proteins are Zn-dependent peptidases with highly conserved residues involved in cation co-ordination. MurNAc-LAA in this family is one of several peptidoglycan hydrolases (PGHs) found in bacterial and bacteriophage or prophage genomes that are involved in the degradation of the peptidoglycan. In Escherichia coli, there are five MurNAc-LAAs present: AmiA, AmiB, AmiC and AmiD that are periplasmic, and AmpD that is cytoplasmic. Three of these (AmiA, AmiB and AmiC) belong to this family, the other two (AmiD and AmpD) do not. E. coli AmiA, AmiB and AmiC play an important role in cleaving the septum to release daughter cells after cell division. In general, bacterial MurNAc-LAAs are members of the bacterial autolytic system and carry a signal peptide in their N-termini that allows their transport across the cytoplasmic membrane. However, the bacteriophage MurNAc-LAAs are endolysins since these phage-encoded enzymes break down bacterial peptidoglycan at the terminal stage of the phage reproduction cycle. As opposed to autolysins, almost all endolysins have no signal peptides and their translocation through the cytoplasmic membrane is thought to proceed with the help of phage-encoded holin proteins. The amidase catalytic module is fused to another functional module (cell wall binding module or CWBM) either at the N- or C-terminus, which is responsible for high affinity binding of the protein to the cell wall.	3.23941e-71
NZ_CP019636.1\|WP_087544697.1\|7260844_7261852_+\|rod-shape-determining-protein	gnl\|CDD\|237562	PRK13927, PRK13927, rod shape-determining protein MreB; Provisional.	0
NZ_CP019636.1\|WP_087544679.1\|7249251_7250112_-\|glutamate-racemase	gnl\|CDD\|234851	PRK00865, PRK00865, glutamate racemase; Provisional.	6.72749e-137
NZ_CP019636.1\|WP_087544685.1\|7253558_7255499_-\|N-acetylmuramoyl-L-alanine-amidase	gnl\|CDD\|119407	cd02696, MurNAc-LAA, N-acetylmuramoyl-L-alanine amidase or MurNAc-LAA (also known as peptidoglycan aminohydrolase, NAMLA amidase, NAMLAA, Amidase 3, and peptidoglycan amidase; EC 3.5.1.28) is an autolysin that hydrolyzes the amide bond between N-acetylmuramoyl and L-amino acids in certain cell wall glycopeptides. These proteins are Zn-dependent peptidases with highly conserved residues involved in cation co-ordination. MurNAc-LAA in this family is one of several peptidoglycan hydrolases (PGHs) found in bacterial and bacteriophage or prophage genomes that are involved in the degradation of the peptidoglycan. In Escherichia coli, there are five MurNAc-LAAs present: AmiA, AmiB, AmiC and AmiD that are periplasmic, and AmpD that is cytoplasmic. Three of these (AmiA, AmiB and AmiC) belong to this family, the other two (AmiD and AmpD) do not. E. coli AmiA, AmiB and AmiC play an important role in cleaving the septum to release daughter cells after cell division. In general, bacterial MurNAc-LAAs are members of the bacterial autolytic system and carry a signal peptide in their N-termini that allows their transport across the cytoplasmic membrane. However, the bacteriophage MurNAc-LAAs are endolysins since these phage-encoded enzymes break down bacterial peptidoglycan at the terminal stage of the phage reproduction cycle. As opposed to autolysins, almost all endolysins have no signal peptides and their translocation through the cytoplasmic membrane is thought to proceed with the help of phage-encoded holin proteins. The amidase catalytic module is fused to another functional module (cell wall binding module or CWBM) either at the N- or C-terminus, which is responsible for high affinity binding of the protein to the cell wall.	1.28442e-75
NZ_CP019636.1\|WP_087544691.1\|7258431_7258845_-\|EVE-domain-containing-protein	gnl\|CDD\|376640	pfam01878, EVE, EVE domain. This domain was formerly known as DUF55. Crystal structures have shown that this domain is part of the PUA superfamily. This domain has been named EVE and is thought to be RNA-binding.	1.06505e-50
NZ_CP019636.1\|WP_087544689.1\|7256918_7258346_-\|cation:proton-antiporter	gnl\|CDD\|223551	COG0475, KefB, Kef-type K+ transport systems, membrane components [Inorganic ion transport and metabolism].	1.55749e-61
NZ_CP019636.1\|WP_087538477.1\|7240326_7241238_-\|IS982-family-transposase	gnl\|CDD\|372648	pfam13612, DDE_Tnp_1_3, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contains three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	6.65467e-97
NZ_CP019636.1\|WP_087544665.1\|7239344_7239614_-\|DUF370-domain-containing-protein	gnl\|CDD\|179823	PRK04323, PRK04323, hypothetical protein; Provisional.	8.34081e-50
NZ_CP019636.1\|WP_087544695.1\|7260109_7260472_-\|single-stranded-DNA-binding-protein	gnl\|CDD\|180986	PRK07459, PRK07459, single-stranded DNA-binding protein; Provisional.	1.34798e-67
NZ_CP019636.1\|WP_087544675.1\|7246993_7247965_-\|solanesyl-diphosphate-synthase	gnl\|CDD\|131796	TIGR02749, Prenyl_transferase, solanesyl diphosphate synthase. Members of this family all are from cyanobacteria or plastid-containing eukaryotes. A member from Arabidopsis (where both plastoquinone and ubiquinone contain the C(45) prenyl moiety) was characterized by heterologous expression as a solanesyl diphosphate synthase. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP019636.1\|WP_087544693.1\|7259292_7260045_+\|DUF541-domain-containing-protein	gnl\|CDD\|225516	COG2968, COG2968, Uncharacterized conserved protein [Function unknown].	4.36349e-63
NZ_CP019636.1\|WP_087544667.1\|7241381_7243709_-\|DUF3488-domain-containing-protein	gnl\|CDD\|224224	COG1305, COG1305, Transglutaminase-like enzymes, putative cysteine proteases [Amino acid transport and metabolism].	2.1208e-24
NZ_CP019636.1\|WP_087544663.1\|7238576_7239179_-\|guanylate-kinase	gnl\|CDD\|234719	PRK00300, gmk, guanylate kinase; Provisional.	6.61129e-107

>NZ_CP019636.1|WP_087544679.1|7249251_7250112_-|glutamate-racemase
MFPSSLFESNLYDFSQAPQRAPIGIFDSGVGGLTVLRQLYRQLPNESIIYFGDTARVPYGIRSQAEIVQFMREILAWMQQQQVKMVVMACNTSSALALETVREEFSLPILDIILPGAKAAVKSGKRIGVIATPATAKSNAYRRAILEINPEVQVWQVGCPEFVPLIEQNRIHDPYTLQVARSYLEPLLQQEIDTLVYGCTHYPHLAPVLRSLLPSHVKLVDPAEYIVAACAKDLDILGLNNNHPPMPTRFAVSGCPQQFAQSSIQWLGHTPMVEAVQLINPAVSSS
>NZ_CP019636.1|WP_087544677.1|7248986_7249184_+|hypothetical-protein
MIYGKMPMMIFILASGYLFAVYLLLALAKKTGRKGTPASGSLTSQGKHKQEVSVAPKVSEATSLH
>NZ_CP019636.1|WP_087544675.1|7246993_7247965_-|solanesyl-diphosphate-synthase
MTPATSLFSPVEADLQILADNLKQLVGNGHPILCAAAEHLFGAGGKRIRPAIVLLISRATMLEQDVTPRHRRLAEITEMIHTASLVHDDVVDESQMRRGVPTVHSLFGNRIAILAGDFLFAQSSWYLANLDNLEVVKLLSEVIMDLAVGEIQQGLSRFDTSISIETYLKKSYYKTASLIANSSKAAGLLSEVPQETAEHLYGYGRHLGLAFQIVDDILDFTSSTDTLGKPAGSDLKSGNLTAPVLFALEEQPYLEVLIEREFAQEGDLEQAMSLIHDSKGIQRARELAEQHANQAVELLADLSSSESRQALIEMADYVLSRLF
>NZ_CP019636.1|WP_087544673.1|7246306_7246780_+|hypothetical-protein
MDLQAQIQLLIDNAPQDGVSPQLVTAIAPALSAIAQKLRHSQYYILQNMEEGWVLTTLSNRANPQLEKRVIYAFPTIQDVPARSSAGLDPRLIAAPMPVTHILFQLVAMEPVDSIVFFETPGTNTDSIEVRRVDLQNLIQQQLQQNRVKREIPPDLA
>NZ_CP019636.1|WP_087544671.1|7244911_7246102_-|heterocyst-differentiation-protein-HetZ
MNSAATITIQGVSSIGVEAIFQLLFKELQQSTKASEHNCRDVATRIAAEVYRICSESKRIQAAGAVENSAMTLARHRLQQCLRYYELGSNRGRIELHSTLSAIIYRYINPPQRQLSYQGRLVVIEDFLQSFYLEALNAFRRENQLGATYRPQSLLELAEYMAFTERYAKRRIPLPGRQQQLIILRAQTFSQQQPPETCVDIEQAAEGSGNEADGSWEDPAVQQLRSAMATQPEPEPQEDTLRSVVITELMNYLEERQQSDCADYFALRLQDLSAQEIESILGLTPRQRDYLQQRFKYHLIRFALLHRWELVHEWLEADLHMNLGLTPQQWEVYTAQLDDKQLSLLELKQQGHPDEKIAKTLGLSMAQLQKRWFKILEQAWEIRNSLVSGSGASTHE
>NZ_CP019636.1|WP_087544669.1|7243938_7244919_-|PatU
MNSDSESLQDQLLTWLLAKNTQTNEQNLVNCKENEGVENLNEIVAAGNGGVFELKSIPQTFQLGETPTVQERFQAVLKRRLQLQIQNHPPLFPWESQLTEYPEYVDNPSIELVPVWGWTAQQSKLNLPIPLPERVFQQLLEKCQAMIASSVPLGAKLVQAVESLFPNDSQALNDLAGMVLRTPSRSVDALETMPNLESNYSDLQPSQQMALSLLAAKQLLENLTLPISATNPVVERQWLTSSGVLTLKVEYQTQGEMTKLRVQSELPSKGIVKLQGDASQATAESSSPGCLSVELHNTQANQTYTLEVDLKEIDQRPLLFVIVPTV
>NZ_CP019636.1|WP_087544667.1|7241381_7243709_-|DUF3488-domain-containing-protein
MFNKPRIGWRLPASLFWRQNMQESPLMEVENSISLRVLVLALVIVGIVATDTACETKFSLWSLPLSTVGAFWSYYRRHNRNVSVKFCIAIGMLVALGAFFGRLFGELNDTRLALAELLIQLQVLHSFDMPRRKDLGYSIVIGLILLGVAATLSQTLAFAPVLLFFLAIALPTLVLDYRSRLGLQPLKMFSGSAWERDHNQKSSSHFFTFYFLLFTLVVGLGLGIFAVLPRFPGYQLRMFPVSSPINIKGDFTGRSIINRGYVRQGHSKNQDRGESHGGEGNQIGEPGLLNDSFYYGFNSRINQNLRGMMKPKVVMRVRSQSSGFWRVLAFDHYTGQGWEISRNEQVQTLKRSPWAYQFFLPFTGLLGKNEEIVQTYTVVSDLPNLIPALASPKEIYFPTPIIAVDTEGSLRSPVELSEDLTYTVISQVPQRDRTLLGKAPTLYPQSIKKYYLQISPAVANKVKQHTEEILANYNIERVGKSQKTLDSPYEKALYLAQYLKQHYSLPKNPADLPYLSDKEDLVEAFLFKYKGGYPDHFSTVLTVMLRSIGIPARLVAGFSPGEFNPFTGMYIVRNTDAYAMTEVYFPNYGWFAFDPIPNHPLIPPSIEDDQTFSVVRQLWTWIAGWLPSPVTGLLNNMFGAIFSWITRILSGFFSLFSRGWLGILTGVILTTALTFLSWIGWGQWREWRDRFALLKLPPMENLYQQMLKWATKKGLGKHPAQTPLEYATGAYQHYSPATAQIIDEICQAYVSWRYGGHAPNLNQLRKRWQELQKNS
>NZ_CP019636.1|WP_087538477.1|7240326_7241238_-|IS982-family-transposase
MSTIVSRLDVTQIFCEVDDFCSSWEKLWQQAPQLPSMTGERRSASRMHISEVMTIAIAFHGSGYRTFKEFYTLQVLPGWRGAFPNLVSYTRFVELMPWCLMLLCCFLHRRRGEITGISFIDSTPIEVCHKCRAHAHKVFKGLVKWGKNSVGWHFGFKLHLIINDQGELLAFKLTPANVDDREPVPDMTKDLIGKLFGDRGYISQKLFEQLYERGLQLVTKSKKNMKNRLVKLIDKILLRKRAVIESVNDHLKNLCQIEHSRHRSVFNFLVNLMAGLAAYTYLPKKPSLDIYPKHLPALPPAVF
>NZ_CP019636.1|WP_087544665.1|7239344_7239614_-|DUF370-domain-containing-protein
MDIQLINIGFGNIVSANRVVAIVSPESAPIKRIITDARDRGQLVDATYGRRTRAVIITDSSHVILSAIQPETVANRFVITRDHHQAVDN
>NZ_CP019636.1|WP_087544663.1|7238576_7239179_-|guanylate-kinase
MMQLTTTKKSGATTQECPDMGKLIILTGPSGVGKGTLMRALLQRHPELHYSVSATTRSPRQGETNGKEYYFVSRREFEQLVAAGELLEWAEFAGNYYGTPKEAVVNQVLSGKRVVLEIELKGARQIRASYPSALSIFILPPSLSELEKRIRGRAQDSEEAIARRMHRAQEEIRAADEFDIQIVNDDFETALNSIEAAIFG
>NZ_CP019636.1|WP_087544681.1|7250707_7252702_-|N-acetylmuramoyl-L-alanine-amidase
MKINWLLPGTFAMTAIFMLLSPAQAAKLQSWRFDASQNQLEINTEGPVQPQAQLVFNPTRLVIDLPGTDSGRPQLIQPVKSSAIRAVRVGQFDGQTTRIVVELTPGYTLDPKQVKFEGKTASRWIVQLPTPQVEQVASSSPNTSFNVYSVVRSGSNSTAHQSTSINNNSVDNNDTVVNTLEGSTQKETVTSNAQGLTQIESLRVTGDGLFVRTNGRSPRIQIFRSSDKSAVNIDILDAALSPRLSQQVVPINKYGVKRVEFTQLKTTPGVRMTLWVDKNSPDWQASTSSFGGLVILPSGDRNKLSRDARDNSSSLVNSDMTTGSVNSRNPNLTSPTSDSLSTIQSVELTASGNQLLIKGDQPLSANGGWDRVSSMFRITIPNAKLAAAVRGPNFDASSPILRVRLQQQDPRTVVVYIQPAAGVQIGQLNQLSGQLLSLELQRSFSPLTPRVSLPPLPRPNPRPLPPITSNPLPMPQPQLRPPVPNGRVVVVVDPGHGGKDSGAPGLGGLLEKDVVLPIGSRIATILQQNGVQVVLTRDADYFVELQGRVDIADRSNADLFVSVHSNSVDGRPDVNGLETYYYDSGLGLARVVHSTILQSIPTLKDRGVRKARFYVLRKSSMPSILVETGYMTGQEDNPRLGSPEYQNRMAEAIANGILLYLRQR
>NZ_CP019636.1|WP_157679687.1|7252830_7253076_+|hypothetical-protein
MLVSTIHPVTRNTHVLNSDRKQRKFPALLLSFFLVKVSVDPHTVTAQALAAKTLITRIKMSIALKCGMIVSFFYAFIAQKM
>NZ_CP019636.1|WP_087544685.1|7253558_7255499_-|N-acetylmuramoyl-L-alanine-amidase
MKIHWLLPGTFVTTSVLMLSSPAQAAKLQSWRFDANQNRLEINTEGPVQPQAQLVFNPTRLVIDLPGTNFGRPQLTQSVGGAIRAVRVGQFDPQTTRIVVELTPGYTLDPNQVKFEGKTASRWTVQLPKPQTERAASSPPSPSSKTPSSSSEEVVISPPKNVYNAVTIESEAEKKPEFSKAVVVAEGTLQVESLQVTGDGFYIRTNGGNPQTQIIRSRDRKTIFIDIPNATLSPNFGNRDRSVNKYGVNRVEMTQLRKTPPAVRMTLRVDKDTPDWRISTSNSGSSAGLVVLPNRYASNLTKNNDSDTSSDNSSNSVVEVATSNSISTIESVELAATGTQLLIKSDQRLSPASTGWDRSSGMYRITIPNAKLASAVKGPNFDASSPILRVRLQQQDPRTVVVYVQPAASVRIGQINQLNSQLLSLELQRNRSITPPIALPAIPRPNPQPLASGTTSKPPAQNPRAPKGRVVIVVDPGHGGKDSGALGIGGIQEKNIILPIGKRVAEILQQNGVQALLTRDSDYFVTLQGRVDIAERANADVFVSVHANSAGDDRPEVSGLETYYYDSGLSLARIVHNSILRSVNVRDRGVRKARFYVLRKNSMPAILVETGYLTGREDAAKLSNRLYQNQMAEAIARGVLQYLKQK
>NZ_CP019636.1|WP_157679688.1|7255759_7255948_+|hypothetical-protein
MVNPHTITAHTLALVPQASFSALIKTQLYRLSFGYNPTLVIEKRIIYLIPIKVLPLGVDVVL
>NZ_CP019636.1|WP_157679689.1|7256361_7256691_-|hypothetical-protein
MDISLAIKQVHLPVNLTTVNSSSMTNWCINHQQSHQINNSFVKDEIGSLPDTLTGVASQQPRRCAYACRRRSTYDGKDSFFREILRAATQGRTLLYSSCISKSHYPAGI
>NZ_CP019636.1|WP_087544689.1|7256918_7258346_-|cation:proton-antiporter
MQLDTITFSFPLLATATETADSSLVLAAVLLSIVVIYLASKVGGELSSRFGLPPVLGELVGGVIVGISVLHLLVFPEGGANSSSSLIMSFLQTTGGLSPDAANAVFTAQSEVISVLAELGVIILLFEIGLESNIKDLIAVGLQATVVAVVGVVVPFTAGTVGLMTLFGVPAVPAIFAGAALTATSIGITSKVLSELGRLNSKEGQIILGAAVIDDVLGIIVLAVVASLAKEGSVDVGKVIYLIISASSFLLGAIVLGSIFSNTFVAIANKLKTRGGLVIPAFIFAFVMAYFAAAIQLEAILGSFAAGLVLDETDERVELQKQVIPIADMLVPIFFVTVGARTDLGVLNPAIPSNREGLVMAIFLIVVAILGKVVTGLSVFGQTQLNRLAIGVGMIPRGEVGLVFLGIGSSIGILSKPLEAAIIMMVIVTTFLAPPFLRFVFPEPKTVSTATEELILNDSSGNSLALESPESQDTK
>NZ_CP019636.1|WP_087544691.1|7258431_7258845_-|EVE-domain-containing-protein
MAYWLLKTEPEEYSYCDLERDGSTVWDGVNNPLALKHLRTMEIGDLVFIYHTGKERQVIGVAEVASQPYPDPKLNDAKRVVVQVRALRKVPQPITLTQIKQDGNFEGFDLLRLTRLSVVPVSESHWQRLLQLTGAMN
>NZ_CP019636.1|WP_087544693.1|7259292_7260045_+|DUF541-domain-containing-protein
MNTDVVSGSQSNTGIWWKVIPLALLICVSCSQAALAQQKERMLRTLTVSGRGMETIPTTLSQVSLGVEVQGKTAQEVQKEAARRSSAVVALLKSRNVEKLQTTGITLNPVYSYSNNVQRITGYAASNIVSFRLPTDRAGTLLDEAVKAGATQISGISFVASDEAIALARQQALKEATQDAQQQAQAVFSGLGFQAKEVVSIEVNGANAPPPPPQPLLRAQSAKLAAQDVSTPIVGGEQQVEATVTLQISY
>NZ_CP019636.1|WP_087544695.1|7260109_7260472_-|single-stranded-DNA-binding-protein
MSINIVTLIGRVGTDPDMKYFESGSVKCKLTLAVNRRTKDREQTDWFNLELWGKTAQVAGDYVRKGRQIAVKGSLKFDTWSDRATGANRSTPVILVDQLQLLGSKRDADEADVDMNPENF
>NZ_CP019636.1|WP_087544697.1|7260844_7261852_+|rod-shape-determining-protein
MGIDLGTANTLVYVSGKGIVLQEPSVVAIDQNEKVALAVGEDAKKMLGRTPGNVVALRPLRDGVIADFDTAELMLKSFIQRVNEGKSLVLPRIVIGIPSGVTGVERRAVMDAASQAGAREVYLIDEPVAAAIGAGLPVAEPTGNMIIDIGGGTTEVAVLSLQGTVLSESVRIAGDELTESIMQYMKKVHNLVIGERTAEDIKIRIGSAYPTHDDDDAMMEVRGLHLLSGLPRTVTIKGPEIRESMSEPLSVIIEAVKRTLERTPPELAADIIDRGIMLAGGGALLKGLDTLISHETGIVTHVAADPLSCVVLGTGRVLENFKQLERVFSGRSRNM

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Crispr_ID: NZ_CP019636_25

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_25

7420369-7420458

Orphan

Consensus_repeat	Method
TCACCCGAACGCGAGTGCGTCTGGTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_25

>merge|NZ_CP019636|25|7420369-7420458|CRISPRCasFinder
TCACCCGAACGCGAGTGCGTCTGGTGACAGGAGAAGGGTTTTCCCGCTCTCACGGCAAGACTGGTCACCCGAACGCGAGTGCGTCTGGTG

>NZ_CP019636|25|24|7420369-7420458|CRISPRCasFinder
TCACCCGAACGCGAGTGCGTCTGGTG	ACAGGAGAAGGGTTTTCCCGCTCTCACGGCAAGACTGG
TCACCCGAACGCGAGTGCGTCTGGTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087545010.1\|7424836_7426219_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226702
NZ_CP019636.1\|WP_087545019.1\|7429330_7430323_-\|folate-binding-protein-YgfZ	unknown	unknown	gnl\|CDD\|223431
NZ_CP019636.1\|WP_087544997.1\|7421053_7421380_+\|30S-ribosomal-protein-S6	unknown	unknown	gnl\|CDD\|275387
NZ_CP019636.1\|WP_087544971.1\|7410973_7412944_+\|acetate--CoA-ligase	unknown	unknown	gnl\|CDD\|234677
NZ_CP019636.1\|WP_087544974.1\|7413045_7414296_-\|competence/damage-inducible-protein-A	unknown	unknown	gnl\|CDD\|234789
NZ_CP019636.1\|WP_087544992.1\|7419305_7420109_-\|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223257
NZ_CP019636.1\|WP_087546460.1\|7422844_7423198_-\|STAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|132914
NZ_CP019636.1\|WP_087545008.1\|7424400_7424850_-\|response-regulator	unknown	unknown	gnl\|CDD\|381108
NZ_CP019636.1\|WP_087544983.1\|7416406_7417690_-\|serine-hydroxymethyltransferase	unknown	unknown	gnl\|CDD\|234571
NZ_CP019636.1\|WP_087545006.1\|7423652_7424285_+\|DedA-family-protein	unknown	unknown	gnl\|CDD\|223659
NZ_CP019636.1\|WP_087545017.1\|7427822_7428155_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239278
NZ_CP019636.1\|WP_087544965.1\|7405209_7408602_+\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|274362
NZ_CP019636.1\|WP_087544986.1\|7418191_7418389_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087544977.1\|7414538_7414895_+\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|379639
NZ_CP019636.1\|WP_087544980.1\|7414989_7416036_-\|undecaprenyl/decaprenyl-phosphate-alpha-N-acetylglucosaminyl-1-phosphate-transferase	unknown	unknown	gnl\|CDD\|133463
NZ_CP019636.1\|WP_087544989.1\|7418563_7419070_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|374405
NZ_CP019636.1\|WP_087545000.1\|7421546_7422104_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275056
NZ_CP019636.1\|WP_087545013.1\|7426524_7427502_+\|cysteine-synthase-A	unknown	unknown	gnl\|CDD\|182672
NZ_CP019636.1\|WP_087544968.1\|7408594_7410466_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226857
NZ_CP019636.1\|WP_087545003.1\|7422096_7422840_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087545010.1\|7424836_7426219_-\|hypothetical-protein	gnl\|CDD\|226702	COG4251, COG4251, Bacteriophytochrome (light-regulated signal transduction histidine kinase) [Signal transduction mechanisms].	2.15352e-55
NZ_CP019636.1\|WP_087544997.1\|7421053_7421380_+\|30S-ribosomal-protein-S6	gnl\|CDD\|275387	cd15487, bS6_chloro_cyano, 30S ribosomal protein S6 of chloroplasts and cyanobacteria. bS6 is one of the components of the small subunit of the prokaryotic ribosome, a ribonucleoprotein organelle that decodes the genetic information in messenger RNA and forms peptide bonds to synthesize the corresponding polypeptides. Mitochondrial and chloroplastic ribosomes are similar to bacterial ribosomes. Ribosomes consist of a large and a small subunit, which assemble during the initiation stage of protein synthesis. Prokaryotic ribosomes consist of three molecules of RNA and more than 50 proteins. The small subunits of bacterial and eukaryotic ribosomes have the same overall shapes (with structural elements described as head, body, platform, beak and shoulder). The bacterial ribosomal protein S6 is important for the assembly of the central domain of the small subunit via heterodimerization with ribosomal protein S18.	5.62903e-51
NZ_CP019636.1\|WP_087544974.1\|7413045_7414296_-\|competence/damage-inducible-protein-A	gnl\|CDD\|234789	PRK00549, PRK00549, competence damage-inducible protein A; Provisional.	0
NZ_CP019636.1\|WP_087544971.1\|7410973_7412944_+\|acetate--CoA-ligase	gnl\|CDD\|234677	PRK00174, PRK00174, acetyl-CoA synthetase; Provisional.	0
NZ_CP019636.1\|WP_087544992.1\|7419305_7420109_-\|fumarylacetoacetate-hydrolase-family-protein	gnl\|CDD\|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	9.51294e-99
NZ_CP019636.1\|WP_087546460.1\|7422844_7423198_-\|STAS-domain-containing-protein	gnl\|CDD\|132914	cd07043, STAS_anti-anti-sigma_factors, Sulphate Transporter and Anti-Sigma factor antagonist) domain of anti-anti-sigma factors, key regulators of anti-sigma factors by phosphorylation. Anti-anti-sigma factors play an important role in the regulation of several sigma factors and their corresponding anti-sigma factors. Upon dephosphorylation they bind the anti-sigma factor and induce the release of the sigma factor from the anti-sigma factor. In a feedback mechanism the anti-anti-sigma factor can be inactivated via phosphorylation by the anti-sigma factor. Well studied examples from Bacillus subtilis are SpoIIAA (regulating sigmaF and sigmaC which play an important role in sporulation) and RsbV (regulating sigmaB involved in the general stress response). The STAS domain is also found in the C- terminal region of sulphate transporters and stressosomes.	1.7825e-24
NZ_CP019636.1\|WP_087545008.1\|7424400_7424850_-\|response-regulator	gnl\|CDD\|381108	cd17557, REC_Rcp-like, phosphoacceptor receiver (REC) domain of cyanobacterial phytochrome response regulator Rcp and similar domains. This family is composed of response regulators (RRs) that are members of phytochrome-associated, light-sensing two-component signal transduction pathways such as Synechocystis sp. Rcp1, Tolypothrix sp. RcpA, and Agrobacterium tumefaciens bacteriophytochrome response regulator AtBRR. They are stand-alone RRs containing only a REC domain with no output/effector domain. The REC domain itself functions as an effector domain. Also included in this family us Methanosaeta harundinacea methanogenesis regulatory protein FilR2, also a stand-alone RR. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	4.80075e-60
NZ_CP019636.1\|WP_087544983.1\|7416406_7417690_-\|serine-hydroxymethyltransferase	gnl\|CDD\|234571	PRK00011, glyA, serine hydroxymethyltransferase; Reviewed.	0
NZ_CP019636.1\|WP_087545006.1\|7423652_7424285_+\|DedA-family-protein	gnl\|CDD\|223659	COG0586, DedA, Uncharacterized membrane-associated protein [Function unknown].	1.24943e-37
NZ_CP019636.1\|WP_087545017.1\|7427822_7428155_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	gnl\|CDD\|239278	cd02980, TRX_Fd_family, Thioredoxin (TRX)-like [2Fe-2S] Ferredoxin (Fd) family; composed of [2Fe-2S] Fds with a TRX fold (TRX-like Fds) and proteins containing domains similar to TRX-like Fd including formate dehydrogenases, NAD-reducing hydrogenases and the subunit E of NADH:ubiquinone oxidoreductase (NuoE). TRX-like Fds are soluble low-potential electron carriers containing a single [2Fe-2S] cluster. The exact role of TRX-like Fd is still unclear. It has been suggested that it may be involved in nitrogen fixation. Its homologous domains in large redox enzymes (such as Nuo and hydrogenases) function as electron carriers.	2.33694e-19
NZ_CP019636.1\|WP_087544965.1\|7405209_7408602_+\|PAS-domain-containing-protein	gnl\|CDD\|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	2.20433e-80
NZ_CP019636.1\|WP_087544977.1\|7414538_7414895_+\|nuclear-transport-factor-2-family-protein	gnl\|CDD\|379639	pfam14534, DUF4440, Domain of unknown function (DUF4440).	2.31059e-10
NZ_CP019636.1\|WP_087544980.1\|7414989_7416036_-\|undecaprenyl/decaprenyl-phosphate-alpha-N-acetylglucosaminyl-1-phosphate-transferase	gnl\|CDD\|133463	cd06853, GT_WecA_like, This subfamily contains Escherichia coli WecA, Bacillus subtilis TagO and related proteins. WecA is an UDP-N-acetylglucosamine (GlcNAc):undecaprenyl-phosphate (Und-P) GlcNAc-1-phosphate transferase that catalyzes the formation of a phosphodiester bond between a membrane-associated undecaprenyl-phosphate molecule and N-acetylglucosamine 1-phosphate, which is usually donated by a soluble UDP-N-acetylglucosamine precursor. WecA participates in the biosynthesis of O antigen LPS in many enteric bacteria and is also involved in the biosynthesis of enterobacterial common antigen. A conserved short sequence motif and a conserved arginine at a cytosolic loop of this integral membrane protein were shown to be critical in recognition of substrate UDP-N-acetylglucosamine.	7.07941e-91
NZ_CP019636.1\|WP_087544989.1\|7418563_7419070_+\|hypothetical-protein	gnl\|CDD\|374405	pfam16166, TIC20, Chloroplast import apparatus Tic20-like. Chloroplast function requires the import of nuclear encoded proteins from the cytoplasm across the chloroplast double membrane. This is accomplished by two protein complexes, the Toc complex located at the outer membrane and the Tic complex located at the inner membrane. The Toc complex recognizes specific proteins by a cleavable N-terminal sequence and is primarily responsible for translocation through the outer membrane, while the Tic complex translocates the protein through the inner membrane. This entry represents Tic20, a core member of the Tic complex. This protein is deeply embedded in the inner envelope membrane and is thought to function as a protein- conducting component of the Tic complex.	7.51325e-19
NZ_CP019636.1\|WP_087545000.1\|7421546_7422104_+\|hypothetical-protein	gnl\|CDD\|275056	TIGR04211, hypothetical_protein, SH3 domain protein. Members of this protein family have a signal peptide, a strongly conserved SH3 domain, a variable region, and then a C-terminal hydrophobic transmembrane alpha helix region.	2.72607e-05
NZ_CP019636.1\|WP_087545013.1\|7426524_7427502_+\|cysteine-synthase-A	gnl\|CDD\|182672	PRK10717, PRK10717, cysteine synthase A; Provisional.	0
NZ_CP019636.1\|WP_087544968.1\|7408594_7410466_-\|hypothetical-protein	gnl\|CDD\|226857	COG4449, COG4449, Predicted protease of the Abi (CAAX) family [General function prediction only].	0
NZ_CP019636.1\|WP_087545019.1\|7429330_7430323_-\|folate-binding-protein-YgfZ	gnl\|CDD\|223431	COG0354, COG0354, Predicted aminomethyltransferase related to GcvT [General function prediction only].	1.56723e-64

>NZ_CP019636.1|WP_087544992.1|7419305_7420109_-|fumarylacetoacetate-hydrolase-family-protein
MAQRYVRVQNPEGQIYYGLLQLSLKVHVLDAPPWLQGQPTDLILEPENYQLLAPCAPSKIVAVGKNYAEHAAEMGTDVPSEPLLFFKPPTSIIASLEEIQYPSQSQRVDYEGELVLVIGDRTFECTPEEAQTKIWGYTIANDVTARDLQKRDSQWTRAKGFDTFCPLGPWIVREVSPAAKLQTFLNEEANPVQCACIDQMVFPPDFLVSYISQVMTLLPGDVILTGTPMGVGPLHPGDRVRVEIEGIGRLENTVIVRQPVQNLTPLK
>NZ_CP019636.1|WP_087544989.1|7418563_7419070_+|hypothetical-protein
MAWRGSTTIQHRLLSCLPYVLPLIEVRQFGDLLFSQFPFLEFLYLPFSPVILLYAYLNQFIPFFDFIVFFALYLLVVRNEKIQHFIRFHTLQALLLSIFIYLCTAVLQLIGIVQQGASLSVPLFGNVIFTLIFLAVVAASIYSIVQAVRGLYAEIPLISQAAYTGTRD
>NZ_CP019636.1|WP_087544986.1|7418191_7418389_+|hypothetical-protein
MLVILMNDQIFAPQQVCQSCLLADGSGQPRWRQGKLHCGHAIRKLTEQQPDQYECIMGFRVANIE
>NZ_CP019636.1|WP_087544983.1|7416406_7417690_-|serine-hydroxymethyltransferase
MTLTNSDFLSSSDPAVAGFINQELQRQRDHLELIASENFASAAVLAAQGSVLTNKYAEGLPGKRYYGGCEFVDKIEQLAIDRAKQLFGAAHANVQPHSGAQANFAVFLTLLEPGDKFMGMDLSHGGHLSHGSPVNVSGKWFQACHYGVNQETEQLDYDQIREQALRERPKLLICGYSAYPRIIDFEKFRSIADEVGAYLLADIAHFAGLVASGLHPSPIPYCDVVTTTTHKTLRGPRGGLILTRDPELGKKLDKSVFPGNQGGPLEHVIAAKAVAFGEALKPEFKTYSAQVIDNARALANQLQKRGLKLVSNGTDNHLMLVDLRSIGMTGKQADQLVSEVNITANKNTVPFDPQSPFVTSGLRLGSPAMTTRGLGVEEFTEIGNIIADRLLNQDSQTVAEDCRRRVKALCDRFPLYSHIVIPVPALA
>NZ_CP019636.1|WP_087544980.1|7414989_7416036_-|undecaprenyl/decaprenyl-phosphate-alpha-N-acetylglucosaminyl-1-phosphate-transferase
MPPQIYHLIAFLCAAVVVLWSTPDVKNIGIKSGRLDKPSDRKVHHRPMVRLGGVSIFAGTIISLLIVWWLGGFGILPTEKEWQIWGVALGGIGFFLIGLADDLLNLSPIARLLMQIVVAAFAWKVGVSIDFLSIPTGGTVQLGWWSLPITVVWLVGMVNAINWIDGLDGLAAGVSGIASVVMLVVALFMQQSAAALIAAAIAGASLGFLRYNFNPAQIFMGDGGAYFMGFTLAAVGVVGLVKTAAVSAVLLPFLILAVPIVDMSAVILARLRRGKSPFVADKSHLHHRLLQAGLSHRLTVLFIYSLTLWVGSLALAIAGIPSGIIYACGATSLLSYTGWKVWKRSRQS
>NZ_CP019636.1|WP_087544977.1|7414538_7414895_+|nuclear-transport-factor-2-family-protein
MQELVKLEEQGWQALSSKGDAAKKFYGSLLTEDAIMIFPSGMLVEGREKILESIGAQPWKSFQMKEPHWILLSEKAAVIVYRVTAQREGSNIYVALISSTYALREGKWKLVVHQQTPI
>NZ_CP019636.1|WP_087544974.1|7413045_7414296_-|competence/damage-inducible-protein-A
MSAEIICVGTELLLGDILNSNAQYLAQQLAKLGIPHYYQTVVGDNPERLKQIIEIASQRVEILIFTGGLGPTPDDLTCETIADFFGVPLVEQPDIIEDITKKYFQRGRVMTPSNRKQALIPQGAKILPNPTGTAPGIIWEPRPGLTIFTFPGVPSEMHRMWEETAVPYLKSQGWGKEIIYSRMLKFWGIAESALAEQVAAYLNLPNPTVAPYSSRGEVKLRVSAKAASVAQAQDFIAPIEKQIREIAGLDYYGADDETLASVVGELLRARGETLSVAESCTGGGLGQMLTEISGSSDYFWGGVISYDNFVKEKLLGVNSQDLAKHGAVSSIVAEQMAQGVQSRLSTTWGLSITGIAGPTGGTETKPVGLVYIGLAGPNGKVESFEYRFGAARGRSLIRHVSACTALDNLRRKLLSQ
>NZ_CP019636.1|WP_087544971.1|7410973_7412944_+|acetate--CoA-ligase
MSQTTIESILQERRLFHPNQNFSQKAQIKSLEDYQRLYDQAKTDPQKFWAELAEQELHWFQKWDTILDWQPPFAKWFVNGKINISYNCLDRHLTTWRKNKAAIIWEGEPGDSRTLTYAQLHREVCQFANVLKQLGVKKGDRVGIYMPMIPEAAIAMLACARIGAPHSVVFGGFSAEALRDRLIDAQAKLVVTADGGWRKDAIVPLKEQVDKALANGAVPSVENVLVVQRTNQEIHMEPGRDHWWHDLQKGVSADCPAEPMDSEDMLFVLYTSGSTGKPKGVVHTTGGYNLYAHMTTKWIFDLQDTDVYWCTADVGWITGHTYIVYGPLSNGATTVMYEGAPRASNPGCTWDIIEKHGVNIFYTAPTAIRAFIKMGEHLPKARNLSSLRLLGTVGEPINPEAWMWYYRVIGGERCPIVDTWWQTETGGIMITPLPGAIPTKPGSATRPFPGILADVVDLEGNPVGDNEGGYLVVRHPWPGMMRTVYGDPERFRRTYWEHIPPQNGQYVYFAGDGARRDEDGYFWVMGRVDDVINVSGHRLGTMEVESALVSHPAVAEAAVVGKPDELKGEDIVAFVTLEGGQQPSEELSKELKQHVVKEIGAIARPGEIRFTDALPKTRSGKIMRRLLRNLAAGQEVSGDTSTLEDRGVLDKLRQGA
>NZ_CP019636.1|WP_087544968.1|7408594_7410466_-|hypothetical-protein
MNLLTVIATAANIISRQFFSRATATQPSNYEIFSRSLLFHSEYYPLNQTVNPQLYRPVAEWSGRLILPVKELHREPFVQFEVQNASAAHHNLIGKVVNLKWSHDPKVQKYVKQVTYDVKFTDKARKNQQTGYVHPTRLNLCPKVDPLESLAGARPVDDVCVKLLRPIVLTHSELETELIINTEPIQVTGRFVGLVTIEARTEAKSDFFLVRHYNKATQSFSDGVQEVVRIPQVPEDRQGISRSTNHDIEKSPFNSHGWYIYGAPDATGTFVVQALEPRALLQLQPQQVISRPKKVLKYLKKEMWARTKAQKGKISRVLLAPDTEAAEAISQWCLGDKALVLHLHGAIGGKKAESPFIKFFAPGHFSYGVAEVVRDFFTHELRFEIIYYQVYTHNVDGVIAGAQTWATFMGSLWQGVLGTRPVCDILTKFPPITTDYNFDGVKFSPLKIFSREITEMMARYRVGDGTGASIITPASSCVQDSNQALYVTIKRIEKLVNSNTTSLAHIQRNSETRQVRDFNALVSLGNALEKELTPLGIVRPDWEKNVQNLSGTGEDFSMLTTIIRALTSWRSIFPRRAQDKIAKIFLHHGAALWVLRTNQVGGFDPNIAPSAPMTLLGRFILFK
>NZ_CP019636.1|WP_087544965.1|7405209_7408602_+|PAS-domain-containing-protein
METDVHDIKILLVDEKLENLNFLSNLFIRQGYRVKTVTSGQQAVNAALAELPDLILLDILMPEISDDINGYEVCQQLKADSKSRDIPIIFISVRDKISEKVKALKLGAVDYITKPVQAEEILVRVENQITIQRLQKQLKQQNARLQNEIQERQQAEAALKASETNHKKSEERLNLAIKASNLGLWDWNLKTGKIYRNCLWTKILGYKEHEIADTRLAFEQLVHPEDLPIVNRSLNDHLQGANPVYEIEFRMRSKSGEWKWILSHGQVVERDNQGKPLRITGIHKDITERKRAEKELRLANERLQHLLSDGPAIIFSAKPTGEYETTFISENVTAILGYTVREFQENPNFWVSHIHPEDRQLVFAGIQQVFKQGCYAHEYRFLHADGTYHWLYDQLRLVCDDANNPIECVGHSTDITERKQAELALRESAERERAIAQVIQRMRQTLDLESIFAATTQELRQVLNCDRVVVYRFHPDWSGEFVAESVGRGWISVIEELQNDSDVTKNAVGNDRCVVQTVNSQDNQVLDTYMQETQGGVYSRGTSFLCVSDIHKAGFDSCYVNLLERLQAKAYITVPIFCGNQLWGLLASYQNSGPRQWKIGEINIAVQIGNQLGVALQQAELLAQTQQQSKALQQAVTAADAANRAKSEFLANMSHELRTPLNAILGFTQLMSHDQKLLAEHQENLGIINRAGEHLLNLINDILEMSKIEAGRTTLDVSSVDLIRLLNNLKEMLRFRATSKGLQLVFEYASDLPQYIQTDASKLRQVLLNLLGNAIKFTERGVVTLRVAVTNGEVLSPPTPYTLQFEVQDTGPGISQEEIENLFEAFKQTETGRNSQQGTGLGLAICRKYVQLMGGEISVRSTVGVGSTFTFDIEIAAADKDELPSNSVSHQIIGLAPNQLEYRILVVDDSRESRLLLVKLLTAIGFSVQEAANGTQAISLWESWCPHLILMDMRMPMMDGYEATRQIKARERERIEKVGEVGGVIASLSSPLHTIIIALTASAFEEQRMLMIEAGCDDFINKPFREELLLEKLSQYLGLKYFYKESNYREGERKKTLNQNLTSNVLLLQLSQMSPEWLTQLNHAAAQGSDDLIFNLIQQIPSQYTQLESALTDLAQNFQFEKIMELVSLI
>NZ_CP019636.1|WP_087544997.1|7421053_7421380_+|30S-ribosomal-protein-S6
MQIIYETMYILRPDLTDEQVEQAIAKYENLLREQGADNIQIQNRGKRRLAYEINRQRDGIYIQMNYTGAGNIIAPLERAMRLSEEVIRYLTIKQEVKEPEAEATATAA
>NZ_CP019636.1|WP_087545000.1|7421546_7422104_+|hypothetical-protein
MSQTDTSTIQALSTEVSKLRQELQLRDQLVQQLSQELFRLVKGNANFMSQPDLSERYLTQVQELREQLQAVEQQVTFYQEQISARDTEIYQLRQSVQELTDRSRMLEQVVQELPQIYRRKFEERMAPVREKVAMLQRENRQLQAEVQSVSYRLALKTRTSSHSGIDLPNFPRTASSQSNISTQNA
>NZ_CP019636.1|WP_087545003.1|7422096_7422840_+|hypothetical-protein
MRKVFILIESDGREITEFPTVRRMLSAIKMAVAEQTSQPTSVEVVAANYFLSEDGILSHSQGQTFSQLQEIICCPLTLSLPDNLSLPFERIIKACRDVTGLRQQLAQQMQVAIGDGCFWLPIVLTAKGPLYGEVITIAEEYNGKKLPENLLICDFSYYQPYHLSDALRQPLYQMAYNLLQSLSAPPATYLVQFGVQTSDICFDRLWPFPTAPALASVGVQQPDLFTCHWYCLTAQPILDLTIMPIVK
>NZ_CP019636.1|WP_087546460.1|7422844_7423198_-|STAS-domain-containing-protein
MTITSECQVVLFKPEGRIDLEGGMTLSEKMAAVVPQRHQLWVIDLAKVDFMDSSGLVSLVKGLKSAHQSGCRLVLCNVQAPVRLILELTQLDSVFEIFNTYDDILTVVQERSLVTVD
>NZ_CP019636.1|WP_087545006.1|7423652_7424285_+|DedA-family-protein
MSLEFISLENIQKVAHEYGYWAIFLGILLENLGIPLPGETVTLVGGFLAGSKELNYWLVLTDAVAGAVIGGTCGYWIGRIGGWSLLVRLGSLFRISEARILTIKEQFSENASKAVFFGRFFALLRIFAAPLAGIVEMSFGKFFIYNLAGAFAWASTMVTLAFFAGRLVSLEQLVAWVSQFAIAALLILVAVIAIPVWLESRQKGGEEIGR
>NZ_CP019636.1|WP_087545008.1|7424400_7424850_-|response-regulator
MAAHNILLVEDDPNDILLLQRAFRKAALTNAALQVVTDGDTAVAYLNGEGEYSDRDHYPLPAVVLLDLKLPCRSGHEILAWLRQQPELKRLPVVVLTSSKQSSDINQAYELGANSYLVKPMGLSALVQVVETLNLYWILLNEKPEIQQY
>NZ_CP019636.1|WP_087545010.1|7424836_7426219_-|hypothetical-protein
MRRPLAQQIQLGLVTTLVLLLVNALVSYRNIQKLSDNERQVSQSHQVIAELKETLSTLKDAETGQRGYLITGKENYLQPYERAIAQITRLIGSLKKLTADNPKQQQQILTLEQAVTNKLAELQQTINIRREQGFGAAQQIVNTNRGKEIMDNIRQQIADMEDFEHRLLQQRSRESQASTQRTIVTLSIATVVNLALLALVYYLFRRNQLQSQQENEILERGVTERTQQLQEANNELEAFGYSVSHDLQAPLRAMHGFAEALLEDYGDLLDELGKEYARRIIASALRLENLIQDLLAYSRLSRTELPLKSIDLTLVISEVIREIQPEIEQKQAEIKIDSPLPQVLAHHPTLVQVATNLVENAIKFVKVGVQPQVRVWAEKYNNWVRLWVADNGIGIASEHQKRIFQVFERLHGQETYPGTGIGLAIVRKGVERMEGRVGVESQLGQGSRFWIELRSPDGST
>NZ_CP019636.1|WP_087545013.1|7426524_7427502_+|cysteine-synthase-A
MDIKNGFVDSIGHTPLIRLNSFSEETGCEILGKAEFLNPGGSVKDRAALYIIQDAEEKGLLKPGGTVVEGTAGNTGIGLAHICNAKGYKCLIIIPNTQSQEKMDALRALGAEVRPVPAVPYKDPNNYVKLSGRVASEMENAIWANQFDNLANRRAHYETTGPEIWAQTDGKVDAWVAATGTGGTFAGVAMYIKEKNPGVKCVVADPKGSGLYSYIKTGEIKIEGNSITEGIGNSRITANMEGAPTDDAIQIDDQEAIRVVYQLLRKDGLFMGGSTGINVAAAVALAKQMGPGHTIVTILCDSGSRYQSRIFNYEWLQSKGLLPDQ
>NZ_CP019636.1|WP_087545017.1|7427822_7428155_+|(2Fe-2S)-ferredoxin-domain-containing-protein
MDSLSQSENSSATPPPVSPKCVRVCQNRTCRKQGAAKVLAAFKALPVPEVTVSGCGCLGQCGNGPIVLVLPDRVWYSHVHPSEIPLVVEQHLRGGQRVTQMLYYRFHVQG
>NZ_CP019636.1|WP_087545019.1|7429330_7430323_-|folate-binding-protein-YgfZ
MSTSGIDANDAAAIQAVQDSVAVCDRSFWGRIKVSDDDRLRFLHNQSTNDIQSLKPGQGCDTVMVSSTARSIDLVTAYIQEDAVLLLVSPNRREFLMGWLDRYIFFADKVQLTDITDETATFSIIGPKSDAVIEKLGAAAIIGQAYGTHISIPSVSASLIAVGSGLATLGYTLILPASDKEKVWSQILEAGAVPMSDRAWEKLRILQGRPAPDHELTEEYNPLEAGLWQTISFNKGCYIGQETIARLNTYKGVKQHLWGVHLSAPAEPESVITIGDEKVGKLTSYTSTFDGHFGLGYIRTKAGGAGLKVHVGEVEGEVVEVPFVSHDYPQ

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Crispr_ID: NZ_CP019636_26

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_26

7713014-7713094

Orphan

Consensus_repeat	Method
TCTTTTCTTAAAGTCAGAAAGTAGGTGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_26

>merge|NZ_CP019636|26|7713014-7713094|CRISPRCasFinder
TCTTTTCTTAAAGTCAGAAAGTAGGTGAGTGATAGATAGCATAATTCATCTCTTCTTTTCTTAAAGTCAGAAAGTAGGTGA

>NZ_CP019636|26|25|7713014-7713094|CRISPRCasFinder
TCTTTTCTTAAAGTCAGAAAGTAGGTGA	GTGATAGATAGCATAATTCATCTCT
TCTTTTCTTAAAGTCAGAAAGTAGGTGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087545471.1\|7711216_7712038_+\|NADPH-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|380322
NZ_CP019636.1\|WP_087545459.1\|7702038_7703178_-\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270273
NZ_CP019636.1\|WP_087545487.1\|7721840_7722989_+\|FMNH2-dependent-alkanesulfonate-monooxygenase	unknown	unknown	gnl\|CDD\|234821
NZ_CP019636.1\|WP_087545479.1\|7717696_7718560_+\|TauD/TfdA-family-dioxygenase	unknown	unknown	gnl\|CDD\|225086
NZ_CP019636.1\|WP_087546477.1\|7714764_7715961_+\|monooxygenase	unknown	unknown	gnl\|CDD\|173852
NZ_CP019636.1\|WP_087545465.1\|7705644_7706685_-\|NADP(H)-dependent-aldo-keto-reductase	unknown	unknown	gnl\|CDD\|381320
NZ_CP019636.1\|WP_087545475.1\|7713875_7714700_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|183055
NZ_CP019636.1\|WP_087545469.1\|7709974_7711090_+\|sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545492.1\|7724095_7724359_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087545483.1\|7719633_7720446_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379312
NZ_CP019636.1\|WP_087545477.1\|7716546_7717614_+\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545455.1\|7700396_7701344_-\|D-2-hydroxyacid-dehydrogenase	unknown	unknown	gnl\|CDD\|240625
NZ_CP019636.1\|WP_087545473.1\|7712125_7712914_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187602
NZ_CP019636.1\|WP_087545467.1\|7707147_7709139_-\|iron-uptake-porin	unknown	unknown	gnl\|CDD\|335962
NZ_CP019636.1\|WP_087545463.1\|7703510_7705157_-\|FAD-binding-protein	unknown	unknown	gnl\|CDD\|223981
NZ_CP019636.1\|WP_087545489.1\|7722998_7723802_+\|aliphatic-sulfonate-ABC-transporter-permease-SsuC	unknown	unknown	gnl\|CDD\|183100
NZ_CP019636.1\|WP_087545457.1\|7701598_7702036_-\|riboflavin-specific-deaminase	unknown	unknown	gnl\|CDD\|238611
NZ_CP019636.1\|WP_087545461.1\|7703184_7703514_-\|4Fe-4S-dicluster-domain-containing-protein	unknown	unknown	gnl\|CDD\|236597
NZ_CP019636.1\|WP_087545481.1\|7718572_7719568_+\|sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545485.1\|7720730_7721783_+\|sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087545471.1\|7711216_7712038_+\|NADPH-dependent-oxidoreductase	gnl\|CDD\|380322	cd02146, NfsA-like, nitroreductase similar to Escherichia coli NfsA. This family contains NADPH-dependent flavin reductase and oxygen-insensitive nitroreductase. These enzymes are homodimeric flavoproteins that contain one FMN per monomer as a cofactor. Flavin reductase catalyzes the reduction of flavin by using NADPH as an electron donor. Oxygen-insensitive nitroreductase, such as NfsA protein in Escherichia coli, catalyzes reduction of nitrocompounds using NADPH as electron donor.	1.24717e-115
NZ_CP019636.1\|WP_087545459.1\|7702038_7703178_-\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270273	cd13555, PBP2_sulfate_ester_like, Sulfate ester binding protein-like, the type 2 periplasmic binding protein fold. This subfamily includes the periplasmic component of putative ABC-type sulfonate transport system similar to SsuA. These domains are found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	8.49311e-43
NZ_CP019636.1\|WP_087545487.1\|7721840_7722989_+\|FMNH2-dependent-alkanesulfonate-monooxygenase	gnl\|CDD\|234821	PRK00719, PRK00719, alkanesulfonate monooxygenase; Provisional.	0
NZ_CP019636.1\|WP_087545479.1\|7717696_7718560_+\|TauD/TfdA-family-dioxygenase	gnl\|CDD\|225086	COG2175, TauD, Probable taurine catabolism dioxygenase [Secondary metabolites biosynthesis, transport, and catabolism].	1.89638e-62
NZ_CP019636.1\|WP_087546477.1\|7714764_7715961_+\|monooxygenase	gnl\|CDD\|173852	cd01163, DszC, Dibenzothiophene (DBT) desulfurization enzyme C. DszC is a flavin reductase dependent enzyme, which catalyzes the first two steps of DBT desulfurization in mesophilic bacteria. DszC converts DBT to DBT-sulfoxide, which is then converted to DBT-sulfone. Bacteria with this enzyme are candidates for the removal of organic sulfur compounds from fossil fuels, which pollute the environment. An equivalent enzyme tdsC, is found in thermophilic bacteria. This alignment also contains a closely related uncharacterized subgroup.	1.32713e-125
NZ_CP019636.1\|WP_087545465.1\|7705644_7706685_-\|NADP(H)-dependent-aldo-keto-reductase	gnl\|CDD\|381320	cd19094, AKR_Tas-like, Escherichia coli Tas protein and similar proteins. Escherichia coli Tas protein is the prototype of this family. It is an NADP(H)-dependent aldo-keto reductase that catalyzes the reversible reduction of ketones to the respective alcohols using NADP(H) as a hydride donor.	0
NZ_CP019636.1\|WP_087545475.1\|7713875_7714700_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|183055	PRK11247, ssuB, aliphatic sulfonates transport ATP-binding subunit; Provisional.	8.18437e-108
NZ_CP019636.1\|WP_087545469.1\|7709974_7711090_+\|sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.65681e-138
NZ_CP019636.1\|WP_087545483.1\|7719633_7720446_+\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	6.02419e-17
NZ_CP019636.1\|WP_087545477.1\|7716546_7717614_+\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.34759e-108
NZ_CP019636.1\|WP_087545455.1\|7700396_7701344_-\|D-2-hydroxyacid-dehydrogenase	gnl\|CDD\|240625	cd05300, 2-Hacid_dh_1, Putative D-isomer specific 2-hydroxyacid dehydrogenase. 2-Hydroxyacid dehydrogenases catalyze the conversion of a wide variety of D-2-hydroxy acids to their corresponding keto acids. The general mechanism is (R)-lactate + acceptor to pyruvate + reduced acceptor. Formate/glycerate and related dehydrogenases of the D-specific 2-hydroxyacid dehydrogenase superfamily include groups such as formate dehydrogenase, glycerate dehydrogenase, L-alanine dehydrogenase, and S-adenosylhomocysteine hydrolase. Despite often low sequence identity, these proteins typically have a characteristic arrangement of 2 similar subdomains of the alpha/beta Rossmann fold NAD+ binding form. The NAD+ binding domain is inserted within the linear sequence of the mostly N-terminal catalytic domain, which has a similar domain structure to the internal NAD binding domain. Structurally, these domains are connected by extended alpha helices and create a cleft in which NAD is bound, primarily to the C-terminal portion of the 2nd (internal) domain. Some related proteins have similar structural subdomains but with a tandem arrangement of the catalytic and NAD-binding subdomains in the linear sequence. While many members of this family are dimeric, alanine DH is hexameric and phosphoglycerate DH is tetrameric. Formate dehydrogenase (FDH) catalyzes the NAD+-dependent oxidation of formate ion to carbon dioxide with the concomitant reduction of NAD+ to NADH. FDHs of this family contain no metal ions or prosthetic groups. Catalysis occurs though direct transfer of the hydride ion to NAD+ without the stages of acid-base catalysis typically found in related dehydrogenases. FDHs are found in all methylotrophic microorganisms in energy production and in the stress responses of plants.	5.47361e-134
NZ_CP019636.1\|WP_087545473.1\|7712125_7712914_+\|SDR-family-oxidoreductase	gnl\|CDD\|187602	cd05344, BKR_like_SDR_like, putative beta-ketoacyl acyl carrier protein [ACP] reductase (BKR)-like, SDR. This subgroup resembles the SDR family, but does not have a perfect match to the NAD-binding motif or the catalytic tetrad characteristic of the SDRs. It includes the SDRs, Q9HYA2 from Pseudomonas aeruginosa PAO1 and APE0912 from Aeropyrum pernix K1. BKR catalyzes the NADPH-dependent reduction of ACP in the first reductive step of de novo fatty acid synthesis (FAS). FAS consists of four elongation steps, which are repeated to extend the fatty acid chain through the addition of two-carbo units from malonyl acyl-carrier protein (ACP): condensation, reduction, dehydration, and a final reduction. Type II FAS, typical of plants and many bacteria, maintains these activities on discrete polypeptides, while type I FAS utilizes one or two multifunctional polypeptides. BKR resembles enoyl reductase, which catalyzes the second reduction step in FAS. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	1.7179e-92
NZ_CP019636.1\|WP_087545467.1\|7707147_7709139_-\|iron-uptake-porin	gnl\|CDD\|335962	pfam04966, OprB, Carbohydrate-selective porin, OprB family.	7.01337e-38
NZ_CP019636.1\|WP_087545463.1\|7703510_7705157_-\|FAD-binding-protein	gnl\|CDD\|223981	COG1053, SdhA, Succinate dehydrogenase/fumarate reductase, flavoprotein subunit [Energy production and conversion].	4.11769e-63
NZ_CP019636.1\|WP_087545489.1\|7722998_7723802_+\|aliphatic-sulfonate-ABC-transporter-permease-SsuC	gnl\|CDD\|183100	PRK11365, ssuC, aliphatic sulfonate ABC transporter permease SsuC.	8.81888e-106
NZ_CP019636.1\|WP_087545457.1\|7701598_7702036_-\|riboflavin-specific-deaminase	gnl\|CDD\|238611	cd01284, Riboflavin_deaminase-reductase, Riboflavin-specific deaminase. Riboflavin biosynthesis protein RibD (Diaminohydroxyphosphoribosylaminopyrimidine deaminase) catalyzes the deamination of 2,5-diamino-6-ribosylamino-4(3H)-pyrimidinone 5'-phosphate, which is an intermediate step in the biosynthesis of riboflavin.The ribG gene of Bacillus subtilis and the ribD gene of E. coli are bifunctional and contain this deaminase domain and a reductase domain which catalyzes the subsequent reduction of the ribosyl side chain.	2.08904e-49
NZ_CP019636.1\|WP_087545461.1\|7703184_7703514_-\|4Fe-4S-dicluster-domain-containing-protein	gnl\|CDD\|236597	PRK09626, oorD, 2-oxoglutarate-acceptor oxidoreductase subunit OorD; Reviewed.	3.80974e-08
NZ_CP019636.1\|WP_087545481.1\|7718572_7719568_+\|sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.75411e-127
NZ_CP019636.1\|WP_087545485.1\|7720730_7721783_+\|sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	6.53258e-126

>NZ_CP019636.1|WP_087545473.1|7712125_7712914_+|SDR-family-oxidoreductase
MDLQLSGKIALVTAASKGLGKATARQFAREGAKVAICARSELVEKAAAEIESETGVDVLAIRADLTKQEDVERVIHATVEKFGGLDILVTNTGGPPAGTLDDVDLTAWEASVNLILLSAVRLIKLSLPHLRKSFSPAILTVTSSSSKQPVQNLILSNSIRLSVIGLTKSLSRELGNDRIRVNSILPGWTYTERVEEIITARTARNGRIPADEIADINATVPLGRMGKPEEFANVAVFLCSPAASYVNGVMLQVDGGLCQGVL
>NZ_CP019636.1|WP_087545471.1|7711216_7712038_+|NADPH-dependent-oxidoreductase
MTNPIELLNHRYGNTSVNADIPWNDSLTTLLSHRSIRSYLPDPLPPGTLEILVAAAQSASTSSNLQTWSVVAVEDAQRKEKLSQLAGNQAHIRQSPLFLVWLADLARLTYIAESRGLPHEGLDYLEMFLMAAIDATLAAQNATVAAESLGLGTVYIGGIRNRPEEVAEVLNLPPHVFAVFGLCVGYPTPEQDVAIKPRLPQSAVLHRETYKLAEQDEAIAQYNEVMKAFYGSQQMNIQSDWSEHSVKRVAFAESLSGRHRLHEALKTLGFQLR
>NZ_CP019636.1|WP_087545469.1|7709974_7711090_+|sulfonate-ABC-transporter-substrate-binding-protein
MYNQGLKHFITQCKSLITSTFFPSGSRNRLLSVLPLPIVGGFVAGLCLSLLFAACSINNSANTPTATSTSAANTQTQASVVRFGYQKSAILIKAKGVLEKRLQPQGVSVEWIEFPAGPQLLEAMNVGSIDFGHTGESPPIFAQAAGASLTYIAGIAASPAGSAVLVPQNSPIKTPTDLKGKKIAFQKGSSAHYMLVQLLDKIGLKYSEIQPVYLPPADARAAFVKGSLDAWVIWDPFYAAAEKAVSARVLVDGKEINKQGGYYLASRKFANENEETIKAILEEIQKLEEWSDKNRDAVAEALSPVLGIDLDTMKKATNRKTFGVVPINEELIGLQQKVADKFYDLKLIPKKIDVREAMLKPEQYAALSPKV
>NZ_CP019636.1|WP_087545467.1|7707147_7709139_-|iron-uptake-porin
MSKICWNSRWIPFLVSLLDIQMILVLNPAKSSANTLESRLSTASSISSTVRSRAMVPRGPAQRAIAPEQHKASVQTNNSVMDHQRLISQVVSPKVERSPSPTSTVANPALKSDSSKPPNDDPAIKHVTSVSELSDVKRSPTPIPANPSLSRDSSKLPNRDATIDQVNSVSQLSDVKPTDWAFQALQSLVERYGVIAGYPNQTFRGNRAMTRYEFAAGLNAALNRITELLAAGTSNLVRKEDLVTLQTLQNQFAAELAQLRGRVDALEAHTASLEQHQFSTTTKFLGEVETVIGGILAGNNVVTKRPAPRIITFQDRVRLIFNTSFTGTDQLRTTLTAGNIASLGGTRTGLFGTTEGRTSDNATPRFPNNDVYLSGLRYQFKPFKNTQVNIFAQSDGAFEIGLSGPINPYFEGSAANAISRYARRNMVYDYGDTGPGIAVLQQFDKQWQLGLAYTAINGDTPTPDNGLFSGRYVALGQLSYYSPSKDFRLALTYANTYSPPNTTGQTGTNFGPVIGSNLANSTVAGTGTVGNLYGIQAFYKINPKFAINGWVGYSAHRYLGRGDGQVWNWAVGLAFPDLLKEGSLGGLFIGMEPKLTALSKNVDLGAGPGQVDKDTSLHIEGFYQYQLNDNIAITPGFIWITAPDFNADNPASLVAWLRTTFKF
>NZ_CP019636.1|WP_087545465.1|7705644_7706685_-|NADP(H)-dependent-aldo-keto-reductase
MKYNQLGESDLKVSEICLGTMTFGQQNTLEDAYQQLDYAVAQGINFIDTAEMYPVPPRAETQGRTETYIGEWLKKQQRDQLIIATKIAGPGRAVKWVRQGALNIELNNIKQAVDDSLKRLQTDYIDLYQIHWPDRYVPLFGQTEYNPKFERETVPIAEQLTAFADLIKAGKIRFLGLSNETPWGVSEFSHIAKQLGLPKVASIQNAYNLLNREFDRYLAEACYYEKIGLLAYSPLGFGLLSGKYFNKPKPENTRLTLFQNFGQRYLKPNVNEAVAAYVEIARKYNLKPAQLAIAFVRSRWFVTSTIIGATSIEQLKENIDSVNVVLDKDILAELDAVHTRYPNPAP
>NZ_CP019636.1|WP_087545463.1|7703510_7705157_-|FAD-binding-protein
MSRNFWSGDSSTTNFDPSLQADVLVMGGGPAGTWAAWSAASSGARVVLVDKGYCGTSGCAAASGNGVWYVPPDPEAREAAMASREALGGFLSNREWMQRVLDQTFANVNLLGEWGYPFPTDDQGKPYRRSLQGPEYMRLMRKQVKRAGVTILDHSPALQLLVDSQGAVAGATGVNRQSGKKWAVRSGAVIIATGGCAFLSKALGCNVLTGDGYLMAVEAGAQMSGMEFSNAYGIAPAFSSVTKTLFYNWATFLYEDGTPIPGAGSQRGRSVIAKTLLTQPVYAILDKATEEMQANMRKAQPNFFLPFDRAGIDPFTQRFPVTLILEGTVRGTGGIKILDSTCATSVPGLYAAGDAATRELICGGFTGGGSHNAAWAISSGYWAGQSAASYTRQLGDQATQRDIEPVGEAAFLNSARSHTLKAEQVIQATQAEVFPYDRNYFRSEQGLTESLHKLNDLWKEVRTSLAVDDNNIVQAREAAAMVATARWMYSSALERRETRGMHRHLDYPQQDAEQQHYLISGGLDKVWVQAQPLNTTVQEPKVEVGATA
>NZ_CP019636.1|WP_087545461.1|7703184_7703514_-|4Fe-4S-dicluster-domain-containing-protein
MIELVSESRCIQCNVCVNVCPTNIFDKVPDAPPSIARQNDCQTCFMCELYCPVDALYVAPQVEPLESVDEKTLVETGLLGSYRQNIGWGRGRENGAKEDSTYQLLKQMK
>NZ_CP019636.1|WP_087545459.1|7702038_7703178_-|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein
MTGKNRVLIANQRPQPSSPGRKGGQGFLSTYTNFLYPPLCSRLSTLVTLVPLLLNTACSSSPTLSQQSTQNLSQRVQNTNTQVASNPSILRLGYISASSGKAPTGPTGWVLHKGKLKPELQKLGIQDVQLLSFPNGPNLNEALVAGAIDVGIYGDTPAIVARATGIPTRLINQEQVGTNAWLVAKKNGPRSVVDLKGQKVATSKGSYMHRYLIGLLQKTNLSQQVTVVHLLPPDAQAALERGNVAAIAAPSGTGPLLKSKGYPVIDEATKHPDLPGTSVTVATEAFLSKHPDFPQKWNKIKQQAVKDIKANSQEYYKFHAQVSGYPLDVVKASYPLEQFPEEPLPTKGQQLLERTKKFLVSQKLAKADFKLTDWIAPQN
>NZ_CP019636.1|WP_087545457.1|7701598_7702036_-|riboflavin-specific-deaminase
MHDEGFMLAALRQSRKALPECLPNPPVGCVIVDADTEEIVAEGYTRAPGKHHAEADALYQIQGKAFNFLKMYVTLEPCSFHGRTPACALAIAQDSRIHEIYVSVVDPDPRNNGQGLNILKKSGKTVYVGLCAHEVNLFINQYLLT
>NZ_CP019636.1|WP_087545455.1|7700396_7701344_-|D-2-hydroxyacid-dehydrogenase
MKLILPVEVADDLKPHLPSDVAVVRVDGDGNLDGDATDAEVYFSWFLLKPNTLNRVLEAAPALRWHHAPNAGVNHILSPTYLERDITLTNGAGVHAIPIAEFVIAFMLAHAKHLHELYTLQDQHQWKRGFPITELWDATLLIIGAGGIGQEIAARAKGFGMKILGSRRHPEPLPNFDKVVGANEWRTLLSEAHYVVIATPLTWETKGLIDETVLRSMRSDAYLMNVARGAVVDEPALITALKEGWIAGAGLDTVISEPLSPESPLWSLPNVFVTPHCTGHSPRVKERTLALFLDNLSRYRNGRPLRNVVDKKAGY
>NZ_CP019636.1|WP_087545475.1|7713875_7714700_+|ATP-binding-cassette-domain-containing-protein
MSLETRGTHLKLERLRKSFGKKAVLQGIDLEIQPGEFVAIVGRSGCGKSTMLRLVAGLDAPSGGNVYLDDKQFHRRINPQVRMMFQDARLLPWQRVLANVELGLINSQSKVYRRQTALHVLRSVGLEDRAHEWPAVLSGGQRQRVALARALVGKPSLLLLDEPLGALDALTRIEMQQLLEDLWKDQKFTALLITHDVEEAVVLADRVVLIEDGLVTMDYHVSLPRPRARGNPVFAQTVEKILQRVMGKQEDKPERNALSQTPQGSDREFAEIIN
>NZ_CP019636.1|WP_087546477.1|7714764_7715961_+|monooxygenase
MVQILEVKETQQSKDWIAIASSLSKELAETAVERDIKAGLPDVEVQRLRETGLLPLIVPKEYGGIGATWVQALKIVQKLSSSDGSIGQLYGNHLNLTALAHVSGTPEQKDRYYRETVEKNLFWANAINTRDTRLKIHPDGENFRVNGVKSFGTGIAVADLRVFSAVQDGVELPFFFVIPKDREGVASHQDWDNIGQRRTDSATFAFDNVLVYKNEILGPPDPPDSGFSTFLGIIAQLTKTYVYLGIAEGAFAAAKEYTSSLTRPWITSGVDTATADPYILHNYGQLWTQLQAAITLADRTAEQVQQAWDKGIELTLQERGEVAISVFAAKAFATKVGLDITSNIFNVTGTRSTATKYGFDRYWRDLRTFTLHDPIDYKLRDIGNWVLNQELPIVTQYS
>NZ_CP019636.1|WP_087545477.1|7716546_7717614_+|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein
MHLKKKFKLTRRSLLFTVGYCLVLSTTLFSCTTSQQTTKQTTQQQIATPNSTERKVVRIVRSKQLTALAVLEKQKTLDKRLEPLGFKVEWPEFAAGPQQLEALNAGSLDIALTAESPPVFAQAAGTDLVYLTAVSFDGKSISLLVPTNSSVKSVKDLKGKKVAFQKASIGHYLLVKALEKEGLKLSDVESVYLPPPDANVAFSQGKVDGWFIWEPFVTRAEQKKIGRVIVDGSQLRDTGNFYSTSRKFYQSNHEVIKIFLEELQKANTWSKEHPKELAQLLAPVTQLDVPTLEKMHDKYDFELRPITEQVIKKQQEVADMWYSQKLIPKKVNVKDGFLTPEEYTKITPQEVLAKQ
>NZ_CP019636.1|WP_087545479.1|7717696_7718560_+|TauD/TfdA-family-dioxygenase
MPTLALTEFKITHLNAPLGSEVTGLDASQAVAPEVILELKQALRDRHILIFKNQNLTDEQFLNFAFYFGSLFVPPDDIPVLASEPGVTPVVIPISNVDGGYTGTREIAFHADHHWTPYPSSGSLLYALEVPPEGGDTYWLNLNLAYETLDESTKQRIADLKLITYNPFLRDPNAPRSKYRLDKSIPLISPVFPHPLVRTHPESGKKILYLGISTEVEIVGVDPQEGAELIEQLREHLNQPRFYYQHKWSVGDIVYWDNQATLHYRQAFAPKYRRVMKRVSLAGSRPF
>NZ_CP019636.1|WP_087545481.1|7718572_7719568_+|sulfonate-ABC-transporter-substrate-binding-protein
MIAKRTLLPSFVASLFVLAATLTSSGLKADSTQISSNTKQTKQTEVRLGYQKGTAFLNIVKARGSLEKRLGSSGVAVKWIEFAQGPPMMEAMSANAVDIGVVGAPPPIFAQAAGTPIVYVASSLPNGNSQVLLVKKDSPFRTVADLKGKKVAVGKGTAGHYLIVKVLESAKLTLKDIQPVYLLPPEARVAFEGGNVDAWVTSDPRYAEIERTGKIRVLATGEKIAEQRSYFIATRSFVDKHPNIVKAILEEQKKDEEWAKSHRKETAKILETATGVKAENWEWSFQRRPNFGVVYLNDQIVKEQQQMADLFYNLKLIPKPVRIKEATWIPQ
>NZ_CP019636.1|WP_087545483.1|7719633_7720446_+|class-I-SAM-dependent-methyltransferase
MTTLPAYDSTLFEGAAWYYARYRPKYPPALFDLLTEKFQLDGTGRLLDLGCGAGLITIPFRDRFEEVIGLDPDPEMLQEAQKQAASVGATNIKWVNERAELVSRALGSFRLVTVGRAFHWMQREIVLERIYELLSDDGGVAIINAPQDIWNSDDPWKKTALTVVKRWLGEQRRTGQGGQGVWKPLEVSHEEILAKSSFTRLEKYELKFEQFWTVDTFLGYLYTTAFCLPSFFGDNREKFEKDLRESLLAVEPSGQFTEELPVIIITARKQ
>NZ_CP019636.1|WP_087545485.1|7720730_7721783_+|sulfonate-ABC-transporter-substrate-binding-protein
MVDEKFLQQRRQFLKSFVKYSLLGLSGFSTPIIGNFLEKAQAQTKTSGINTNVVRLGYQTYGDIVRLKGVLEQPLKALGVDIDWAPFPAGPQLLEAMSAGRVDIGSVGETPPIFAQAAGAQLVYIAGRKPSKGEGSGLIVRQDSPIKRVADLKGQKVVFQKGSASHYLLLRALQEAGLKYSDIQPISLTPAEARDAFIQKKIDAWVTWDPFYAFVQKTANARTLRNAAGIATQGGFYLARREFAVQNPGVVKVVLEEIDKLGQWAEANPTEVVKLLAPELKLDPAILEVAVRRRTYTLRKLTPNLISEQQRIADVFYQEKVIPRKIDIKQALLTTQQYTALTPPRLLSQR
>NZ_CP019636.1|WP_087545487.1|7721840_7722989_+|FMNH2-dependent-alkanesulfonate-monooxygenase
MVEAFWYLPTQGDERYLGTKIGSREANYPYMRQIAQAVDQLGYGGMLIGTGQKQDTWIVAASLIPVTQRLRFLVAFRPSIMSPSLSARMAATFDQISNGRIILNVVTGGDSEELAKDGVFLDHDERYELTDEFLTIWRSLMLGEEVNFSGRHLKAKGAKLQFSPVQKPHPTLYFGGSSDAALRVAAKHIDVYLTWGEPPQQVAEKIAKVRHLAAEQGRTVRFGIRMHVIVRETTSQAWDAANDLIKYVDEKTIAAAQQRFARSDSEGQRRMVQLHQGSRKQLEISPNLWSGVGLARGGAGTALVGDPDTVAVRILEYTDLGIDTFVLSGYPHLEEAYRVAELVFPRLPLQNLPTFASPQALNNPYNEFVNKSDLLQPQPTAS
>NZ_CP019636.1|WP_087545489.1|7722998_7723802_+|aliphatic-sulfonate-ABC-transporter-permease-SsuC
MAIALKFKSNIFHNRQIQSLIPWGVPILLLVVWQLLSTIGVIPTRILPAPLSVVGAAIKLAETGELFRNIGISAARAISGFIVGGSIGFALGLLNGISPIAEKLLDTSLQMLRNIPNLALIPLVILWFGIGDEARLFLVSLGVMFPIYLNTFHGIRSVDPGLIEMGRVYGLTAWGLFWRIILPGAMSSILVGVRFSLGIMWLTLIVAETIAADSGIGYMAMNAREFMQTDVVVLSILLYALFGKLADVIARYLERYWLQWHPNYQNV
>NZ_CP019636.1|WP_087545492.1|7724095_7724359_+|hypothetical-protein
MLSFAIDALRLRLTHPTKNSIRLLKILEFQPQNLELQPQNLKVHPQNLKVHPQNLKVHPQNSKLHPQNLKVHPQNLKVHPQNLKVHP

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Crispr_ID: NZ_CP019636_27

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_27

7724018-7724128

Orphan

Consensus_repeat	Method
AGTACCCATGCTGTCCTTTGCAATTGATGCGTTACGGCTA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_27

>merge|NZ_CP019636|27|7724018-7724128|CRISPRCasFinder
AGTACCCATGCTGTCCTTTGCAATTGATGCGTTACGGCTATTCTTTGATTGAGTGCACGGCTGAAGAAACAAGTACCCATGCTGTCCTTTGCAATTGATGCGTTACGGCTA

>NZ_CP019636|27|26|7724018-7724128|CRISPRCasFinder
AGTACCCATGCTGTCCTTTGCAATTGATGCGTTACGGCTA	TTCTTTGATTGAGTGCACGGCTGAAGAAACA
AGTACCCATGCTGTCCTTTGCAATTGATGCGTTACGGCTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087545526.1\|7740957_7742859_+\|scytonemin-biosynthesis-protein-ScyA	unknown	unknown	gnl\|CDD\|223107
NZ_CP019636.1\|WP_087545483.1\|7719633_7720446_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379312
NZ_CP019636.1\|WP_087545510.1\|7734866_7735559_-\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP019636.1\|WP_087545487.1\|7721840_7722989_+\|FMNH2-dependent-alkanesulfonate-monooxygenase	unknown	unknown	gnl\|CDD\|234821
NZ_CP019636.1\|WP_087545513.1\|7736837_7737668_-\|response-regulator	unknown	unknown	gnl\|CDD\|381093
NZ_CP019636.1\|WP_087545498.1\|7730197_7730470_+\|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	unknown	unknown	gnl\|CDD\|225170
NZ_CP019636.1\|WP_087546477.1\|7714764_7715961_+\|monooxygenase	unknown	unknown	gnl\|CDD\|173852
NZ_CP019636.1\|WP_087545485.1\|7720730_7721783_+\|sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545475.1\|7713875_7714700_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|183055
NZ_CP019636.1\|WP_087546479.1\|7727150_7728224_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|224586
NZ_CP019636.1\|WP_087545507.1\|7733951_7734644_-\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP019636.1\|WP_087545477.1\|7716546_7717614_+\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545473.1\|7712125_7712914_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187602
NZ_CP019636.1\|WP_087545479.1\|7717696_7718560_+\|TauD/TfdA-family-dioxygenase	unknown	unknown	gnl\|CDD\|225086
NZ_CP019636.1\|WP_087545501.1\|7730647_7732504_-\|molybdate-ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224043
NZ_CP019636.1\|WP_087545489.1\|7722998_7723802_+\|aliphatic-sulfonate-ABC-transporter-permease-SsuC	unknown	unknown	gnl\|CDD\|183100
NZ_CP019636.1\|WP_087545504.1\|7732748_7733573_-\|molybdate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270255
NZ_CP019636.1\|WP_087545481.1\|7718572_7719568_+\|sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545495.1\|7729369_7729579_-\|transporter	unknown	unknown	gnl\|CDD\|226113
NZ_CP019636.1\|WP_087545516.1\|7737733_7739707_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|223715

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087545526.1\|7740957_7742859_+\|scytonemin-biosynthesis-protein-ScyA	gnl\|CDD\|223107	COG0028, IlvB, Thiamine pyrophosphate-requiring enzymes [acetolactate synthase, pyruvate dehydrogenase (cytochrome), glyoxylate carboligase, phosphonopyruvate decarboxylase] [Amino acid transport and metabolism / Coenzyme metabolism].	1.65524e-130
NZ_CP019636.1\|WP_087545483.1\|7719633_7720446_+\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	6.02419e-17
NZ_CP019636.1\|WP_087545510.1\|7734866_7735559_-\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	4.14159e-46
NZ_CP019636.1\|WP_087545487.1\|7721840_7722989_+\|FMNH2-dependent-alkanesulfonate-monooxygenase	gnl\|CDD\|234821	PRK00719, PRK00719, alkanesulfonate monooxygenase; Provisional.	0
NZ_CP019636.1\|WP_087545513.1\|7736837_7737668_-\|response-regulator	gnl\|CDD\|381093	cd17538, REC_D1_PleD-like, first (D1) phosphoacceptor receiver (REC) domain of response regulator PleD and similar domains. PleD contains a REC domain (D1) with the phosphorylatable aspartate, a REC-like adaptor domain (D2), and the enzymatic diguanylate cyclase (DGC) domain, also called the GGDEF domain according to a conserved sequence motif, as its output domain. The GGDEF-containing PleD response regulators are global regulators of cell metabolism in some important human pathogens. This model describes D1 of PleD and similar domains. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	3.43854e-34
NZ_CP019636.1\|WP_087545498.1\|7730197_7730470_+\|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	gnl\|CDD\|225170	COG2261, COG2261, Predicted membrane protein [Function unknown].	5.34844e-12
NZ_CP019636.1\|WP_087546477.1\|7714764_7715961_+\|monooxygenase	gnl\|CDD\|173852	cd01163, DszC, Dibenzothiophene (DBT) desulfurization enzyme C. DszC is a flavin reductase dependent enzyme, which catalyzes the first two steps of DBT desulfurization in mesophilic bacteria. DszC converts DBT to DBT-sulfoxide, which is then converted to DBT-sulfone. Bacteria with this enzyme are candidates for the removal of organic sulfur compounds from fossil fuels, which pollute the environment. An equivalent enzyme tdsC, is found in thermophilic bacteria. This alignment also contains a closely related uncharacterized subgroup.	1.32713e-125
NZ_CP019636.1\|WP_087545485.1\|7720730_7721783_+\|sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	6.53258e-126
NZ_CP019636.1\|WP_087545475.1\|7713875_7714700_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|183055	PRK11247, ssuB, aliphatic sulfonates transport ATP-binding subunit; Provisional.	8.18437e-108
NZ_CP019636.1\|WP_087546479.1\|7727150_7728224_-\|ATP-binding-protein	gnl\|CDD\|224586	COG1672, COG1672, Predicted ATPase (AAA+ superfamily) [General function prediction only].	2.10206e-09
NZ_CP019636.1\|WP_087545507.1\|7733951_7734644_-\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	6.21569e-41
NZ_CP019636.1\|WP_087545477.1\|7716546_7717614_+\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.34759e-108
NZ_CP019636.1\|WP_087545473.1\|7712125_7712914_+\|SDR-family-oxidoreductase	gnl\|CDD\|187602	cd05344, BKR_like_SDR_like, putative beta-ketoacyl acyl carrier protein [ACP] reductase (BKR)-like, SDR. This subgroup resembles the SDR family, but does not have a perfect match to the NAD-binding motif or the catalytic tetrad characteristic of the SDRs. It includes the SDRs, Q9HYA2 from Pseudomonas aeruginosa PAO1 and APE0912 from Aeropyrum pernix K1. BKR catalyzes the NADPH-dependent reduction of ACP in the first reductive step of de novo fatty acid synthesis (FAS). FAS consists of four elongation steps, which are repeated to extend the fatty acid chain through the addition of two-carbo units from malonyl acyl-carrier protein (ACP): condensation, reduction, dehydration, and a final reduction. Type II FAS, typical of plants and many bacteria, maintains these activities on discrete polypeptides, while type I FAS utilizes one or two multifunctional polypeptides. BKR resembles enoyl reductase, which catalyzes the second reduction step in FAS. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	1.7179e-92
NZ_CP019636.1\|WP_087545479.1\|7717696_7718560_+\|TauD/TfdA-family-dioxygenase	gnl\|CDD\|225086	COG2175, TauD, Probable taurine catabolism dioxygenase [Secondary metabolites biosynthesis, transport, and catabolism].	1.89638e-62
NZ_CP019636.1\|WP_087545501.1\|7730647_7732504_-\|molybdate-ABC-transporter-permease-subunit	gnl\|CDD\|224043	COG1118, CysA, ABC-type sulfate/molybdate transport systems, ATPase component [Inorganic ion transport and metabolism].	3.75124e-130
NZ_CP019636.1\|WP_087545489.1\|7722998_7723802_+\|aliphatic-sulfonate-ABC-transporter-permease-SsuC	gnl\|CDD\|183100	PRK11365, ssuC, aliphatic sulfonate ABC transporter permease SsuC.	8.81888e-106
NZ_CP019636.1\|WP_087545504.1\|7732748_7733573_-\|molybdate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270255	cd13537, PBP2_YvgL_like, Substrate binding domain of putative molybdate-binding protein YvgL and similar proteins;the type 2 periplasmic binding protein fold. This subfamily contains domains found in ModA proteins of putative ABC-type transporter. ModA proteins serve as initial receptors in the ABC transport of molybdate in eubacteria and archaea. Bacteria and archaea import molybdenum and tungsten from the environment in the form of the oxyanions molybdate (MoO(4) (2-)) and tungstate (WO(4) (2-)). After binding molybdate and tungstate with high affinity, they interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The ModA proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	2.32886e-110
NZ_CP019636.1\|WP_087545481.1\|7718572_7719568_+\|sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.75411e-127
NZ_CP019636.1\|WP_087545495.1\|7729369_7729579_-\|transporter	gnl\|CDD\|226113	COG3585, MopI, Molybdopterin-binding protein [Coenzyme metabolism].	1.68858e-20
NZ_CP019636.1\|WP_087545516.1\|7737733_7739707_-\|PAS-domain-S-box-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	9.57992e-52

>NZ_CP019636.1|WP_087545489.1|7722998_7723802_+|aliphatic-sulfonate-ABC-transporter-permease-SsuC
MAIALKFKSNIFHNRQIQSLIPWGVPILLLVVWQLLSTIGVIPTRILPAPLSVVGAAIKLAETGELFRNIGISAARAISGFIVGGSIGFALGLLNGISPIAEKLLDTSLQMLRNIPNLALIPLVILWFGIGDEARLFLVSLGVMFPIYLNTFHGIRSVDPGLIEMGRVYGLTAWGLFWRIILPGAMSSILVGVRFSLGIMWLTLIVAETIAADSGIGYMAMNAREFMQTDVVVLSILLYALFGKLADVIARYLERYWLQWHPNYQNV
>NZ_CP019636.1|WP_087545487.1|7721840_7722989_+|FMNH2-dependent-alkanesulfonate-monooxygenase
MVEAFWYLPTQGDERYLGTKIGSREANYPYMRQIAQAVDQLGYGGMLIGTGQKQDTWIVAASLIPVTQRLRFLVAFRPSIMSPSLSARMAATFDQISNGRIILNVVTGGDSEELAKDGVFLDHDERYELTDEFLTIWRSLMLGEEVNFSGRHLKAKGAKLQFSPVQKPHPTLYFGGSSDAALRVAAKHIDVYLTWGEPPQQVAEKIAKVRHLAAEQGRTVRFGIRMHVIVRETTSQAWDAANDLIKYVDEKTIAAAQQRFARSDSEGQRRMVQLHQGSRKQLEISPNLWSGVGLARGGAGTALVGDPDTVAVRILEYTDLGIDTFVLSGYPHLEEAYRVAELVFPRLPLQNLPTFASPQALNNPYNEFVNKSDLLQPQPTAS
>NZ_CP019636.1|WP_087545485.1|7720730_7721783_+|sulfonate-ABC-transporter-substrate-binding-protein
MVDEKFLQQRRQFLKSFVKYSLLGLSGFSTPIIGNFLEKAQAQTKTSGINTNVVRLGYQTYGDIVRLKGVLEQPLKALGVDIDWAPFPAGPQLLEAMSAGRVDIGSVGETPPIFAQAAGAQLVYIAGRKPSKGEGSGLIVRQDSPIKRVADLKGQKVVFQKGSASHYLLLRALQEAGLKYSDIQPISLTPAEARDAFIQKKIDAWVTWDPFYAFVQKTANARTLRNAAGIATQGGFYLARREFAVQNPGVVKVVLEEIDKLGQWAEANPTEVVKLLAPELKLDPAILEVAVRRRTYTLRKLTPNLISEQQRIADVFYQEKVIPRKIDIKQALLTTQQYTALTPPRLLSQR
>NZ_CP019636.1|WP_087545483.1|7719633_7720446_+|class-I-SAM-dependent-methyltransferase
MTTLPAYDSTLFEGAAWYYARYRPKYPPALFDLLTEKFQLDGTGRLLDLGCGAGLITIPFRDRFEEVIGLDPDPEMLQEAQKQAASVGATNIKWVNERAELVSRALGSFRLVTVGRAFHWMQREIVLERIYELLSDDGGVAIINAPQDIWNSDDPWKKTALTVVKRWLGEQRRTGQGGQGVWKPLEVSHEEILAKSSFTRLEKYELKFEQFWTVDTFLGYLYTTAFCLPSFFGDNREKFEKDLRESLLAVEPSGQFTEELPVIIITARKQ
>NZ_CP019636.1|WP_087545481.1|7718572_7719568_+|sulfonate-ABC-transporter-substrate-binding-protein
MIAKRTLLPSFVASLFVLAATLTSSGLKADSTQISSNTKQTKQTEVRLGYQKGTAFLNIVKARGSLEKRLGSSGVAVKWIEFAQGPPMMEAMSANAVDIGVVGAPPPIFAQAAGTPIVYVASSLPNGNSQVLLVKKDSPFRTVADLKGKKVAVGKGTAGHYLIVKVLESAKLTLKDIQPVYLLPPEARVAFEGGNVDAWVTSDPRYAEIERTGKIRVLATGEKIAEQRSYFIATRSFVDKHPNIVKAILEEQKKDEEWAKSHRKETAKILETATGVKAENWEWSFQRRPNFGVVYLNDQIVKEQQQMADLFYNLKLIPKPVRIKEATWIPQ
>NZ_CP019636.1|WP_087545479.1|7717696_7718560_+|TauD/TfdA-family-dioxygenase
MPTLALTEFKITHLNAPLGSEVTGLDASQAVAPEVILELKQALRDRHILIFKNQNLTDEQFLNFAFYFGSLFVPPDDIPVLASEPGVTPVVIPISNVDGGYTGTREIAFHADHHWTPYPSSGSLLYALEVPPEGGDTYWLNLNLAYETLDESTKQRIADLKLITYNPFLRDPNAPRSKYRLDKSIPLISPVFPHPLVRTHPESGKKILYLGISTEVEIVGVDPQEGAELIEQLREHLNQPRFYYQHKWSVGDIVYWDNQATLHYRQAFAPKYRRVMKRVSLAGSRPF
>NZ_CP019636.1|WP_087545477.1|7716546_7717614_+|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein
MHLKKKFKLTRRSLLFTVGYCLVLSTTLFSCTTSQQTTKQTTQQQIATPNSTERKVVRIVRSKQLTALAVLEKQKTLDKRLEPLGFKVEWPEFAAGPQQLEALNAGSLDIALTAESPPVFAQAAGTDLVYLTAVSFDGKSISLLVPTNSSVKSVKDLKGKKVAFQKASIGHYLLVKALEKEGLKLSDVESVYLPPPDANVAFSQGKVDGWFIWEPFVTRAEQKKIGRVIVDGSQLRDTGNFYSTSRKFYQSNHEVIKIFLEELQKANTWSKEHPKELAQLLAPVTQLDVPTLEKMHDKYDFELRPITEQVIKKQQEVADMWYSQKLIPKKVNVKDGFLTPEEYTKITPQEVLAKQ
>NZ_CP019636.1|WP_087546477.1|7714764_7715961_+|monooxygenase
MVQILEVKETQQSKDWIAIASSLSKELAETAVERDIKAGLPDVEVQRLRETGLLPLIVPKEYGGIGATWVQALKIVQKLSSSDGSIGQLYGNHLNLTALAHVSGTPEQKDRYYRETVEKNLFWANAINTRDTRLKIHPDGENFRVNGVKSFGTGIAVADLRVFSAVQDGVELPFFFVIPKDREGVASHQDWDNIGQRRTDSATFAFDNVLVYKNEILGPPDPPDSGFSTFLGIIAQLTKTYVYLGIAEGAFAAAKEYTSSLTRPWITSGVDTATADPYILHNYGQLWTQLQAAITLADRTAEQVQQAWDKGIELTLQERGEVAISVFAAKAFATKVGLDITSNIFNVTGTRSTATKYGFDRYWRDLRTFTLHDPIDYKLRDIGNWVLNQELPIVTQYS
>NZ_CP019636.1|WP_087545475.1|7713875_7714700_+|ATP-binding-cassette-domain-containing-protein
MSLETRGTHLKLERLRKSFGKKAVLQGIDLEIQPGEFVAIVGRSGCGKSTMLRLVAGLDAPSGGNVYLDDKQFHRRINPQVRMMFQDARLLPWQRVLANVELGLINSQSKVYRRQTALHVLRSVGLEDRAHEWPAVLSGGQRQRVALARALVGKPSLLLLDEPLGALDALTRIEMQQLLEDLWKDQKFTALLITHDVEEAVVLADRVVLIEDGLVTMDYHVSLPRPRARGNPVFAQTVEKILQRVMGKQEDKPERNALSQTPQGSDREFAEIIN
>NZ_CP019636.1|WP_087545473.1|7712125_7712914_+|SDR-family-oxidoreductase
MDLQLSGKIALVTAASKGLGKATARQFAREGAKVAICARSELVEKAAAEIESETGVDVLAIRADLTKQEDVERVIHATVEKFGGLDILVTNTGGPPAGTLDDVDLTAWEASVNLILLSAVRLIKLSLPHLRKSFSPAILTVTSSSSKQPVQNLILSNSIRLSVIGLTKSLSRELGNDRIRVNSILPGWTYTERVEEIITARTARNGRIPADEIADINATVPLGRMGKPEEFANVAVFLCSPAASYVNGVMLQVDGGLCQGVL
>NZ_CP019636.1|WP_087546479.1|7727150_7728224_-|ATP-binding-protein
MTSGSLPSNPFVAAGMIEDPRLFVGRKDELQAIASRMSGVQPTSVNVVGDKRIGKSSLLYHFFQTWEQRVADSSRYVVIYLSLQNVQCHRETDFYQAIAQKLLSFPRVATNPALSDSLRVTPLNRLAFSAAMGEWKTQGVLPVLCLDDFKMLFDNKSEFDDGFYNNLRSLMDNNMLMLVVGTTKELDFYRKQHQLTSSFFNLGHVLKLGELKEEEAKDLARLPASTVNTASAALSMDEQHLTRQLGGRHPFLLQIAGGLVCEARQQGHDENWVKSRFEEQKRRLPKSRNASLKLSNLWRWVHKIFSSIGAFGLWLAEFWNNAKTVVLGIVMVVLVIYCLQNPDKVQEFLAYLLNLTK
>NZ_CP019636.1|WP_087545495.1|7729369_7729579_-|transporter
MQVSARNALKATVKKVVEGSVNNEIVLEVAPGVEVTAIITKSSAEKLQLKEGKQAYAIIKSSDVMVAVD
>NZ_CP019636.1|WP_087545498.1|7730197_7730470_+|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein
MNILAWIILGLLAGAIAKAIYPGHQGGGILGTILLGIIGAFVGGSLGLYFSTGTFTLAAPALSIPGVIVAVVGALVAVFVWNLLTRRSAV
>NZ_CP019636.1|WP_087545501.1|7730647_7732504_-|molybdate-ABC-transporter-permease-subunit
MPLDLSPLWISLKTSLLATFITFFFGIAAAYWMLGYRGKGKSLIEGIFVAPLILPPTVVGFLLLILFGKNGPLGKLMEPLGLSVVFTWYGAAIAATVVAFPLMYKTALGAFEQIDSNLLRVARTLGAKESTIFWRISLPLAVPGILAATILAFARALGEFGATLMLAGNIPGQTQTIPMAIYFAVEGGAMNEAWFWAVAIIAISLSGIIAVNYWQEKQDKRRGQGRAGDAGDAGGAGDAGGARDAGGENTVPFLGRPTYHSSDSGLFVDIEKQLPGFHLKVSFSADAQPLGLLGGSGAGKSMILRCIAGIETPTSGRIVLNGRVLFDSQQGINLPPRDRRIGFLVQNYALFPHMTVAQNILFGLPKGLSNTAIRQLLKTQLTTVQLEGLAERYPHQLSGGQQQRVALARALASQPEALLLDEPFSALDTHLRSQLEQQMVGTLANYEGVTLFVTHNMEEAYRVCPNLLVLEKGKAVHYGTKYEIFEHPATVSVAQLTGCKNFSRAVAVTSQQVKAIDWDCTLRVMEPMPNTLSNVGIRAHHLMISNDPHQENTFECWLVRTSETPHRMTLFLKLHHPSSNPNDYHLQAEVFKEKWANLKDQPMPWYVHLDPLRLILMQ
>NZ_CP019636.1|WP_087545504.1|7732748_7733573_-|molybdate-ABC-transporter-substrate-binding-protein
MKRRQFFAFIGIAVASSLLAVGLQLFDSSIVTAQPNTTNLLVSAAASLKDGLEEIKTVYQQSKPNVNLSYNFGASGALQQQIEQGAPADIFISAGKKQMDALEQKGLLVSGTRTNLANNSLVLVVPSNSTGVTSFNTLADAKVKKIAIGEPRSVPAGQYGEQVLQKLNLLQTVKPKLVYANNVRQVLASVESGNADAGLVYATDAKISDKVKVVVVADDKSHSPIVYPMAVLKSSKNVDAAKEFVQFLSSEPAKTVLKKYGFIVQVSKAPAPSR
>NZ_CP019636.1|WP_087545507.1|7733951_7734644_-|acyltransferase
MNTKKNFFRWKRLQESLLTHLLGNIPTRAVGGNLRNTLYRTIFARIGRSVYIEESVKFINTLCIEIGNGVDILKGVSINATGHINNRVYLGNKVTLEHGVDIRAMKDTCVYIDEGTYIGPYVCLAGPGNIKIGRRCLIAAHVGIFANNHIFDNPMLDIEDQGVTRQGIVIEDDCWIGHAVTVLDGVTIGKGSVIGAGGVVTKDIPPFSIAVGVPAKVIKSRKKEAVSSKD
>NZ_CP019636.1|WP_087545510.1|7734866_7735559_-|acyltransferase
MNREQSSSKLQRLQELLVIGLLGNLPTIALGPKLRSIVYRNIFARMGKSVYIQDGVEFLGASSIEMGNGVFIFKGVRLDARGNQNKLYLDNGVAIERNVNIGRLENTHIEIGQETFIGPGVCIAGPGDIKIGKRCLIAANSGIYANNHNFADPIEPIKYQGISRKGIVIGDDCWLGHGVAVLDGVTIGEGSVIGAGAVVTKDIPPFSVAVGVPAKVIKSRTSKQLVNTRD
>NZ_CP019636.1|WP_087545513.1|7736837_7737668_-|response-regulator
MMHESSKKILIIEDDAITRNIFLDGLEAEGFDTIGAENGTFGIQKAQEHQPDLVICDIKMPGMDGFGVLTMLRQDPVTAIIPFIFLTGSDHNTSLRKGMELGADDYITKPCTVQQLVRAVAVRLEKQVKLMQYWYAACYEKLSVSVASGTTSSMEAVSIFPSVPQLKEVFDYIEANYHQGITLCDVAEAVGYSSAYLTNRVAKITGETVNGWIVKRRMSAARCLLQETDQTIEQIASSLGYQNACHFSRQFRQHHGVPPQTWRKEHQLIRRCKVEV
>NZ_CP019636.1|WP_087545516.1|7737733_7739707_-|PAS-domain-S-box-protein
MTFRDYMLSNTGSQSALQPEEELKLAQFLINQLADAAFYVGANAQIIYVNDAICRMTEYSREELLSMTLTDMDIDISPHNWSEKWVTLKQQGSLTFKSRYRTKAGRIFLVQMSVTYVEHQAKEFGCVFARDSSDELVGLSLQQYVNKTPNPNEELQQEVIEYQKTETELETSLSLLRSTLESTANGILAVNFEGEILCYNHKFMEMWQFPNSVSVSRKCNRAKAFFESKVKDPELFRQAVWEMSSQSEKESYDVVELKDGRVFAHYSEPQRLGDKIIGRVWSIWDVTESRKTEEALRLNEARFRALAETTEASIFLTQNKNICYVNPAAEELTGYTRKELLDDFNIDHLIKGKKLRQVTKLDGAACCEYQEIQILTKNGTNRWLACTIGVLDGVLDFASQSVELVTAIDITDYKQAESEVRQALEQAKRLSELRERFVSMLCHQFRTPLNVVSFSADLLRRHIHQWTEEKNRSYLDLIQVAVQQISELLDEILLYGQAESARLECEPRPLDLDRFCRDIIAQVQLASGNQKSVNFITQGNCSTAYLDPKLLQHILTNLLSNAIKYSPTSSTVSFRLCCQKKQAIFQVKDSGIGIPVIDQQQIFEPFYRGSNVDSIPGTGLGLSIVKTLVDLHGGEIAVESLVGVGTTFTVKLPSTDS
>NZ_CP019636.1|WP_087545526.1|7740957_7742859_+|scytonemin-biosynthesis-protein-ScyA
MSENYTQITSQIGDQPYEVYQPNGCVQSEPVGCTHHFEDQPNTHSNTTPVVKEQIQRSLTVADAIAQMMEDLGVNCAFGVNGGAMAGLWGSLSNSLLQVLNFRHEAGAAFAAAEAYFATSRPCVVFTTAGPGITNALTGLFAARGEGAKVILLSACTSSPQRGRWAIQETSTDTLPTEGIFTSGALFNYATTVESAAQLPQIFRKLALGLSQPGGFVAHLSIPTAVQTSPLDDVPLFQGIYCSLVTPDQETIIRTAQLLSEGPFAIWVGFGARSAAKEILQLAERTGAAVMCSPRGKGIFPEDHPQFVGVTGLGGHASVMTYMQQQTPLRTLVLGTRLSEPTSFWNPLLVPPGGFVHVDIDPTVPGVAYSQAETFAIQSDIKAFLQGLLQHDDLLASAAVTAFWLPRPEKEAMQSGPDSPVRPEILLEAIQKVIVQNSDAIVLAECGNSFLWSTHLLQFSQPHRYRISTGVGAMGHAAAGVVGAAVARNGKAVAIVGDGAMLMNNEINTAVKYQIPAVWIVLNDARYNMSYQGMAMLGLKGADALIPEADFAMIARGMGAEGIRINKEDDLEAALEQAMAANGPIVVDVVINADRRAPSKGRNQGLASQGVKSTPVQKTELHMSFPQVSFPNV

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Crispr_ID: NZ_CP019636_28

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_28

7726495-7726704

Orphan

Consensus_repeat	Method
CACGCCNANCGCCACGCC	CRT

5 spacers

The CRISPR arrays of NZ_CP019636_28

>merge|NZ_CP019636|28|7726495-7726704|CRT
CACGCCTACCGCCACGCCTACCGCCACGCCTACCGCCACGCCTACCGCCACGCCTCCCGCCACGCCTCCCGCCACACCAAACGCCACGCCTACCGCCACGCCTCCCGCCACGCCTCCCGCCACGCCTAACGCCACGCCTAACGCCACGCCTAACGCCACGCCAAACGCCACGCCAAACGCCACGCCAAACGCCACGCCAAACGCCACGCC

>NZ_CP019636|28|8|7726495-7726704|CRT
CACGCCTACCGCCACGCC	TACCGCCACGCCTACCGC
CACGCCTACCGCCACGCC	TCCCGCCACGCCTCCCGCCACACCAAACGC
CACGCCTACCGCCACGCC	TCCCGCCACGCCTCCCGC
CACGCCTAACGCCACGCC	TAACGCCACGCCTAACGC
CACGCCAAACGCCACGCC	AAACGCCACGCCAAACGC
CACGCCAAACGCCACGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087545526.1\|7740957_7742859_+\|scytonemin-biosynthesis-protein-ScyA	unknown	unknown	gnl\|CDD\|223107
NZ_CP019636.1\|WP_087545483.1\|7719633_7720446_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379312
NZ_CP019636.1\|WP_087545492.1\|7724095_7724359_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087545487.1\|7721840_7722989_+\|FMNH2-dependent-alkanesulfonate-monooxygenase	unknown	unknown	gnl\|CDD\|234821
NZ_CP019636.1\|WP_087545513.1\|7736837_7737668_-\|response-regulator	unknown	unknown	gnl\|CDD\|381093
NZ_CP019636.1\|WP_087545498.1\|7730197_7730470_+\|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	unknown	unknown	gnl\|CDD\|225170
NZ_CP019636.1\|WP_087546477.1\|7714764_7715961_+\|monooxygenase	unknown	unknown	gnl\|CDD\|173852
NZ_CP019636.1\|WP_087545485.1\|7720730_7721783_+\|sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545475.1\|7713875_7714700_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|183055
NZ_CP019636.1\|WP_087546479.1\|7727150_7728224_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|224586
NZ_CP019636.1\|WP_087545507.1\|7733951_7734644_-\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP019636.1\|WP_087545477.1\|7716546_7717614_+\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545495.1\|7729369_7729579_-\|transporter	unknown	unknown	gnl\|CDD\|226113
NZ_CP019636.1\|WP_087545479.1\|7717696_7718560_+\|TauD/TfdA-family-dioxygenase	unknown	unknown	gnl\|CDD\|225086
NZ_CP019636.1\|WP_087545501.1\|7730647_7732504_-\|molybdate-ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224043
NZ_CP019636.1\|WP_087545489.1\|7722998_7723802_+\|aliphatic-sulfonate-ABC-transporter-permease-SsuC	unknown	unknown	gnl\|CDD\|183100
NZ_CP019636.1\|WP_087545504.1\|7732748_7733573_-\|molybdate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270255
NZ_CP019636.1\|WP_087545510.1\|7734866_7735559_-\|acyltransferase	unknown	unknown	gnl\|CDD\|100053
NZ_CP019636.1\|WP_087545481.1\|7718572_7719568_+\|sulfonate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270275
NZ_CP019636.1\|WP_087545516.1\|7737733_7739707_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|223715

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087545526.1\|7740957_7742859_+\|scytonemin-biosynthesis-protein-ScyA	gnl\|CDD\|223107	COG0028, IlvB, Thiamine pyrophosphate-requiring enzymes [acetolactate synthase, pyruvate dehydrogenase (cytochrome), glyoxylate carboligase, phosphonopyruvate decarboxylase] [Amino acid transport and metabolism / Coenzyme metabolism].	1.65524e-130
NZ_CP019636.1\|WP_087545483.1\|7719633_7720446_+\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	6.02419e-17
NZ_CP019636.1\|WP_087545510.1\|7734866_7735559_-\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	4.14159e-46
NZ_CP019636.1\|WP_087545487.1\|7721840_7722989_+\|FMNH2-dependent-alkanesulfonate-monooxygenase	gnl\|CDD\|234821	PRK00719, PRK00719, alkanesulfonate monooxygenase; Provisional.	0
NZ_CP019636.1\|WP_087545513.1\|7736837_7737668_-\|response-regulator	gnl\|CDD\|381093	cd17538, REC_D1_PleD-like, first (D1) phosphoacceptor receiver (REC) domain of response regulator PleD and similar domains. PleD contains a REC domain (D1) with the phosphorylatable aspartate, a REC-like adaptor domain (D2), and the enzymatic diguanylate cyclase (DGC) domain, also called the GGDEF domain according to a conserved sequence motif, as its output domain. The GGDEF-containing PleD response regulators are global regulators of cell metabolism in some important human pathogens. This model describes D1 of PleD and similar domains. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	3.43854e-34
NZ_CP019636.1\|WP_087545498.1\|7730197_7730470_+\|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein	gnl\|CDD\|225170	COG2261, COG2261, Predicted membrane protein [Function unknown].	5.34844e-12
NZ_CP019636.1\|WP_087546477.1\|7714764_7715961_+\|monooxygenase	gnl\|CDD\|173852	cd01163, DszC, Dibenzothiophene (DBT) desulfurization enzyme C. DszC is a flavin reductase dependent enzyme, which catalyzes the first two steps of DBT desulfurization in mesophilic bacteria. DszC converts DBT to DBT-sulfoxide, which is then converted to DBT-sulfone. Bacteria with this enzyme are candidates for the removal of organic sulfur compounds from fossil fuels, which pollute the environment. An equivalent enzyme tdsC, is found in thermophilic bacteria. This alignment also contains a closely related uncharacterized subgroup.	1.32713e-125
NZ_CP019636.1\|WP_087545485.1\|7720730_7721783_+\|sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	6.53258e-126
NZ_CP019636.1\|WP_087545475.1\|7713875_7714700_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|183055	PRK11247, ssuB, aliphatic sulfonates transport ATP-binding subunit; Provisional.	8.18437e-108
NZ_CP019636.1\|WP_087546479.1\|7727150_7728224_-\|ATP-binding-protein	gnl\|CDD\|224586	COG1672, COG1672, Predicted ATPase (AAA+ superfamily) [General function prediction only].	2.10206e-09
NZ_CP019636.1\|WP_087545507.1\|7733951_7734644_-\|acyltransferase	gnl\|CDD\|100053	cd04647, LbH_MAT_like, Maltose O-acyltransferase (MAT)-like: This family is composed of maltose O-acetyltransferase, galactoside O-acetyltransferase (GAT), xenobiotic acyltransferase (XAT) and similar proteins. MAT and GAT catalyze the CoA-dependent acetylation of the 6-hydroxyl group of their respective sugar substrates. MAT acetylates maltose and glucose exclusively while GAT specifically acetylates galactopyranosides. XAT catalyzes the CoA-dependent acetylation of a variety of hydroxyl-bearing acceptors such as chloramphenicol and streptogramin, among others. XATs are implicated in inactivating xenobiotics leading to xenobiotic resistance in patients. Members of this family contain a a left-handed parallel beta-helix (LbH) domain with at least 5 turns, each containing three imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X). They are trimeric in their active form.	6.21569e-41
NZ_CP019636.1\|WP_087545477.1\|7716546_7717614_+\|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	3.34759e-108
NZ_CP019636.1\|WP_087545495.1\|7729369_7729579_-\|transporter	gnl\|CDD\|226113	COG3585, MopI, Molybdopterin-binding protein [Coenzyme metabolism].	1.68858e-20
NZ_CP019636.1\|WP_087545479.1\|7717696_7718560_+\|TauD/TfdA-family-dioxygenase	gnl\|CDD\|225086	COG2175, TauD, Probable taurine catabolism dioxygenase [Secondary metabolites biosynthesis, transport, and catabolism].	1.89638e-62
NZ_CP019636.1\|WP_087545501.1\|7730647_7732504_-\|molybdate-ABC-transporter-permease-subunit	gnl\|CDD\|224043	COG1118, CysA, ABC-type sulfate/molybdate transport systems, ATPase component [Inorganic ion transport and metabolism].	3.75124e-130
NZ_CP019636.1\|WP_087545489.1\|7722998_7723802_+\|aliphatic-sulfonate-ABC-transporter-permease-SsuC	gnl\|CDD\|183100	PRK11365, ssuC, aliphatic sulfonate ABC transporter permease SsuC.	8.81888e-106
NZ_CP019636.1\|WP_087545504.1\|7732748_7733573_-\|molybdate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270255	cd13537, PBP2_YvgL_like, Substrate binding domain of putative molybdate-binding protein YvgL and similar proteins;the type 2 periplasmic binding protein fold. This subfamily contains domains found in ModA proteins of putative ABC-type transporter. ModA proteins serve as initial receptors in the ABC transport of molybdate in eubacteria and archaea. Bacteria and archaea import molybdenum and tungsten from the environment in the form of the oxyanions molybdate (MoO(4) (2-)) and tungstate (WO(4) (2-)). After binding molybdate and tungstate with high affinity, they interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The ModA proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	2.32886e-110
NZ_CP019636.1\|WP_087545481.1\|7718572_7719568_+\|sulfonate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270275	cd13557, PBP2_SsuA, Substrate binding domain of sulfonate binding protein, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes the sulfonate binding domains SsuA found in eubacterial SsuA proteins that serve as initial receptors in the ABC transport of bicarbonate, nitrate, taurine, or a wide range of aliphatic sulfonates, while other closest homologs are involved in thiamine (vitamin B1) biosynthetic pathway and desulfurization (DszB). After binding the ligand, SsuA interacts 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. The SsuA proteins belong to the PBPII superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.75411e-127
NZ_CP019636.1\|WP_087545516.1\|7737733_7739707_-\|PAS-domain-S-box-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	9.57992e-52

>NZ_CP019636.1|WP_087545492.1|7724095_7724359_+|hypothetical-protein
MLSFAIDALRLRLTHPTKNSIRLLKILEFQPQNLELQPQNLKVHPQNLKVHPQNLKVHPQNSKLHPQNLKVHPQNLKVHPQNLKVHP
>NZ_CP019636.1|WP_087545489.1|7722998_7723802_+|aliphatic-sulfonate-ABC-transporter-permease-SsuC
MAIALKFKSNIFHNRQIQSLIPWGVPILLLVVWQLLSTIGVIPTRILPAPLSVVGAAIKLAETGELFRNIGISAARAISGFIVGGSIGFALGLLNGISPIAEKLLDTSLQMLRNIPNLALIPLVILWFGIGDEARLFLVSLGVMFPIYLNTFHGIRSVDPGLIEMGRVYGLTAWGLFWRIILPGAMSSILVGVRFSLGIMWLTLIVAETIAADSGIGYMAMNAREFMQTDVVVLSILLYALFGKLADVIARYLERYWLQWHPNYQNV
>NZ_CP019636.1|WP_087545487.1|7721840_7722989_+|FMNH2-dependent-alkanesulfonate-monooxygenase
MVEAFWYLPTQGDERYLGTKIGSREANYPYMRQIAQAVDQLGYGGMLIGTGQKQDTWIVAASLIPVTQRLRFLVAFRPSIMSPSLSARMAATFDQISNGRIILNVVTGGDSEELAKDGVFLDHDERYELTDEFLTIWRSLMLGEEVNFSGRHLKAKGAKLQFSPVQKPHPTLYFGGSSDAALRVAAKHIDVYLTWGEPPQQVAEKIAKVRHLAAEQGRTVRFGIRMHVIVRETTSQAWDAANDLIKYVDEKTIAAAQQRFARSDSEGQRRMVQLHQGSRKQLEISPNLWSGVGLARGGAGTALVGDPDTVAVRILEYTDLGIDTFVLSGYPHLEEAYRVAELVFPRLPLQNLPTFASPQALNNPYNEFVNKSDLLQPQPTAS
>NZ_CP019636.1|WP_087545485.1|7720730_7721783_+|sulfonate-ABC-transporter-substrate-binding-protein
MVDEKFLQQRRQFLKSFVKYSLLGLSGFSTPIIGNFLEKAQAQTKTSGINTNVVRLGYQTYGDIVRLKGVLEQPLKALGVDIDWAPFPAGPQLLEAMSAGRVDIGSVGETPPIFAQAAGAQLVYIAGRKPSKGEGSGLIVRQDSPIKRVADLKGQKVVFQKGSASHYLLLRALQEAGLKYSDIQPISLTPAEARDAFIQKKIDAWVTWDPFYAFVQKTANARTLRNAAGIATQGGFYLARREFAVQNPGVVKVVLEEIDKLGQWAEANPTEVVKLLAPELKLDPAILEVAVRRRTYTLRKLTPNLISEQQRIADVFYQEKVIPRKIDIKQALLTTQQYTALTPPRLLSQR
>NZ_CP019636.1|WP_087545483.1|7719633_7720446_+|class-I-SAM-dependent-methyltransferase
MTTLPAYDSTLFEGAAWYYARYRPKYPPALFDLLTEKFQLDGTGRLLDLGCGAGLITIPFRDRFEEVIGLDPDPEMLQEAQKQAASVGATNIKWVNERAELVSRALGSFRLVTVGRAFHWMQREIVLERIYELLSDDGGVAIINAPQDIWNSDDPWKKTALTVVKRWLGEQRRTGQGGQGVWKPLEVSHEEILAKSSFTRLEKYELKFEQFWTVDTFLGYLYTTAFCLPSFFGDNREKFEKDLRESLLAVEPSGQFTEELPVIIITARKQ
>NZ_CP019636.1|WP_087545481.1|7718572_7719568_+|sulfonate-ABC-transporter-substrate-binding-protein
MIAKRTLLPSFVASLFVLAATLTSSGLKADSTQISSNTKQTKQTEVRLGYQKGTAFLNIVKARGSLEKRLGSSGVAVKWIEFAQGPPMMEAMSANAVDIGVVGAPPPIFAQAAGTPIVYVASSLPNGNSQVLLVKKDSPFRTVADLKGKKVAVGKGTAGHYLIVKVLESAKLTLKDIQPVYLLPPEARVAFEGGNVDAWVTSDPRYAEIERTGKIRVLATGEKIAEQRSYFIATRSFVDKHPNIVKAILEEQKKDEEWAKSHRKETAKILETATGVKAENWEWSFQRRPNFGVVYLNDQIVKEQQQMADLFYNLKLIPKPVRIKEATWIPQ
>NZ_CP019636.1|WP_087545479.1|7717696_7718560_+|TauD/TfdA-family-dioxygenase
MPTLALTEFKITHLNAPLGSEVTGLDASQAVAPEVILELKQALRDRHILIFKNQNLTDEQFLNFAFYFGSLFVPPDDIPVLASEPGVTPVVIPISNVDGGYTGTREIAFHADHHWTPYPSSGSLLYALEVPPEGGDTYWLNLNLAYETLDESTKQRIADLKLITYNPFLRDPNAPRSKYRLDKSIPLISPVFPHPLVRTHPESGKKILYLGISTEVEIVGVDPQEGAELIEQLREHLNQPRFYYQHKWSVGDIVYWDNQATLHYRQAFAPKYRRVMKRVSLAGSRPF
>NZ_CP019636.1|WP_087545477.1|7716546_7717614_+|aliphatic-sulfonate-ABC-transporter-substrate-binding-protein
MHLKKKFKLTRRSLLFTVGYCLVLSTTLFSCTTSQQTTKQTTQQQIATPNSTERKVVRIVRSKQLTALAVLEKQKTLDKRLEPLGFKVEWPEFAAGPQQLEALNAGSLDIALTAESPPVFAQAAGTDLVYLTAVSFDGKSISLLVPTNSSVKSVKDLKGKKVAFQKASIGHYLLVKALEKEGLKLSDVESVYLPPPDANVAFSQGKVDGWFIWEPFVTRAEQKKIGRVIVDGSQLRDTGNFYSTSRKFYQSNHEVIKIFLEELQKANTWSKEHPKELAQLLAPVTQLDVPTLEKMHDKYDFELRPITEQVIKKQQEVADMWYSQKLIPKKVNVKDGFLTPEEYTKITPQEVLAKQ
>NZ_CP019636.1|WP_087546477.1|7714764_7715961_+|monooxygenase
MVQILEVKETQQSKDWIAIASSLSKELAETAVERDIKAGLPDVEVQRLRETGLLPLIVPKEYGGIGATWVQALKIVQKLSSSDGSIGQLYGNHLNLTALAHVSGTPEQKDRYYRETVEKNLFWANAINTRDTRLKIHPDGENFRVNGVKSFGTGIAVADLRVFSAVQDGVELPFFFVIPKDREGVASHQDWDNIGQRRTDSATFAFDNVLVYKNEILGPPDPPDSGFSTFLGIIAQLTKTYVYLGIAEGAFAAAKEYTSSLTRPWITSGVDTATADPYILHNYGQLWTQLQAAITLADRTAEQVQQAWDKGIELTLQERGEVAISVFAAKAFATKVGLDITSNIFNVTGTRSTATKYGFDRYWRDLRTFTLHDPIDYKLRDIGNWVLNQELPIVTQYS
>NZ_CP019636.1|WP_087545475.1|7713875_7714700_+|ATP-binding-cassette-domain-containing-protein
MSLETRGTHLKLERLRKSFGKKAVLQGIDLEIQPGEFVAIVGRSGCGKSTMLRLVAGLDAPSGGNVYLDDKQFHRRINPQVRMMFQDARLLPWQRVLANVELGLINSQSKVYRRQTALHVLRSVGLEDRAHEWPAVLSGGQRQRVALARALVGKPSLLLLDEPLGALDALTRIEMQQLLEDLWKDQKFTALLITHDVEEAVVLADRVVLIEDGLVTMDYHVSLPRPRARGNPVFAQTVEKILQRVMGKQEDKPERNALSQTPQGSDREFAEIIN
>NZ_CP019636.1|WP_087546479.1|7727150_7728224_-|ATP-binding-protein
MTSGSLPSNPFVAAGMIEDPRLFVGRKDELQAIASRMSGVQPTSVNVVGDKRIGKSSLLYHFFQTWEQRVADSSRYVVIYLSLQNVQCHRETDFYQAIAQKLLSFPRVATNPALSDSLRVTPLNRLAFSAAMGEWKTQGVLPVLCLDDFKMLFDNKSEFDDGFYNNLRSLMDNNMLMLVVGTTKELDFYRKQHQLTSSFFNLGHVLKLGELKEEEAKDLARLPASTVNTASAALSMDEQHLTRQLGGRHPFLLQIAGGLVCEARQQGHDENWVKSRFEEQKRRLPKSRNASLKLSNLWRWVHKIFSSIGAFGLWLAEFWNNAKTVVLGIVMVVLVIYCLQNPDKVQEFLAYLLNLTK
>NZ_CP019636.1|WP_087545495.1|7729369_7729579_-|transporter
MQVSARNALKATVKKVVEGSVNNEIVLEVAPGVEVTAIITKSSAEKLQLKEGKQAYAIIKSSDVMVAVD
>NZ_CP019636.1|WP_087545498.1|7730197_7730470_+|GlsB/YeaQ/YmgE-family-stress-response-membrane-protein
MNILAWIILGLLAGAIAKAIYPGHQGGGILGTILLGIIGAFVGGSLGLYFSTGTFTLAAPALSIPGVIVAVVGALVAVFVWNLLTRRSAV
>NZ_CP019636.1|WP_087545501.1|7730647_7732504_-|molybdate-ABC-transporter-permease-subunit
MPLDLSPLWISLKTSLLATFITFFFGIAAAYWMLGYRGKGKSLIEGIFVAPLILPPTVVGFLLLILFGKNGPLGKLMEPLGLSVVFTWYGAAIAATVVAFPLMYKTALGAFEQIDSNLLRVARTLGAKESTIFWRISLPLAVPGILAATILAFARALGEFGATLMLAGNIPGQTQTIPMAIYFAVEGGAMNEAWFWAVAIIAISLSGIIAVNYWQEKQDKRRGQGRAGDAGDAGGAGDAGGARDAGGENTVPFLGRPTYHSSDSGLFVDIEKQLPGFHLKVSFSADAQPLGLLGGSGAGKSMILRCIAGIETPTSGRIVLNGRVLFDSQQGINLPPRDRRIGFLVQNYALFPHMTVAQNILFGLPKGLSNTAIRQLLKTQLTTVQLEGLAERYPHQLSGGQQQRVALARALASQPEALLLDEPFSALDTHLRSQLEQQMVGTLANYEGVTLFVTHNMEEAYRVCPNLLVLEKGKAVHYGTKYEIFEHPATVSVAQLTGCKNFSRAVAVTSQQVKAIDWDCTLRVMEPMPNTLSNVGIRAHHLMISNDPHQENTFECWLVRTSETPHRMTLFLKLHHPSSNPNDYHLQAEVFKEKWANLKDQPMPWYVHLDPLRLILMQ
>NZ_CP019636.1|WP_087545504.1|7732748_7733573_-|molybdate-ABC-transporter-substrate-binding-protein
MKRRQFFAFIGIAVASSLLAVGLQLFDSSIVTAQPNTTNLLVSAAASLKDGLEEIKTVYQQSKPNVNLSYNFGASGALQQQIEQGAPADIFISAGKKQMDALEQKGLLVSGTRTNLANNSLVLVVPSNSTGVTSFNTLADAKVKKIAIGEPRSVPAGQYGEQVLQKLNLLQTVKPKLVYANNVRQVLASVESGNADAGLVYATDAKISDKVKVVVVADDKSHSPIVYPMAVLKSSKNVDAAKEFVQFLSSEPAKTVLKKYGFIVQVSKAPAPSR
>NZ_CP019636.1|WP_087545507.1|7733951_7734644_-|acyltransferase
MNTKKNFFRWKRLQESLLTHLLGNIPTRAVGGNLRNTLYRTIFARIGRSVYIEESVKFINTLCIEIGNGVDILKGVSINATGHINNRVYLGNKVTLEHGVDIRAMKDTCVYIDEGTYIGPYVCLAGPGNIKIGRRCLIAAHVGIFANNHIFDNPMLDIEDQGVTRQGIVIEDDCWIGHAVTVLDGVTIGKGSVIGAGGVVTKDIPPFSIAVGVPAKVIKSRKKEAVSSKD
>NZ_CP019636.1|WP_087545510.1|7734866_7735559_-|acyltransferase
MNREQSSSKLQRLQELLVIGLLGNLPTIALGPKLRSIVYRNIFARMGKSVYIQDGVEFLGASSIEMGNGVFIFKGVRLDARGNQNKLYLDNGVAIERNVNIGRLENTHIEIGQETFIGPGVCIAGPGDIKIGKRCLIAANSGIYANNHNFADPIEPIKYQGISRKGIVIGDDCWLGHGVAVLDGVTIGEGSVIGAGAVVTKDIPPFSVAVGVPAKVIKSRTSKQLVNTRD
>NZ_CP019636.1|WP_087545513.1|7736837_7737668_-|response-regulator
MMHESSKKILIIEDDAITRNIFLDGLEAEGFDTIGAENGTFGIQKAQEHQPDLVICDIKMPGMDGFGVLTMLRQDPVTAIIPFIFLTGSDHNTSLRKGMELGADDYITKPCTVQQLVRAVAVRLEKQVKLMQYWYAACYEKLSVSVASGTTSSMEAVSIFPSVPQLKEVFDYIEANYHQGITLCDVAEAVGYSSAYLTNRVAKITGETVNGWIVKRRMSAARCLLQETDQTIEQIASSLGYQNACHFSRQFRQHHGVPPQTWRKEHQLIRRCKVEV
>NZ_CP019636.1|WP_087545516.1|7737733_7739707_-|PAS-domain-S-box-protein
MTFRDYMLSNTGSQSALQPEEELKLAQFLINQLADAAFYVGANAQIIYVNDAICRMTEYSREELLSMTLTDMDIDISPHNWSEKWVTLKQQGSLTFKSRYRTKAGRIFLVQMSVTYVEHQAKEFGCVFARDSSDELVGLSLQQYVNKTPNPNEELQQEVIEYQKTETELETSLSLLRSTLESTANGILAVNFEGEILCYNHKFMEMWQFPNSVSVSRKCNRAKAFFESKVKDPELFRQAVWEMSSQSEKESYDVVELKDGRVFAHYSEPQRLGDKIIGRVWSIWDVTESRKTEEALRLNEARFRALAETTEASIFLTQNKNICYVNPAAEELTGYTRKELLDDFNIDHLIKGKKLRQVTKLDGAACCEYQEIQILTKNGTNRWLACTIGVLDGVLDFASQSVELVTAIDITDYKQAESEVRQALEQAKRLSELRERFVSMLCHQFRTPLNVVSFSADLLRRHIHQWTEEKNRSYLDLIQVAVQQISELLDEILLYGQAESARLECEPRPLDLDRFCRDIIAQVQLASGNQKSVNFITQGNCSTAYLDPKLLQHILTNLLSNAIKYSPTSSTVSFRLCCQKKQAIFQVKDSGIGIPVIDQQQIFEPFYRGSNVDSIPGTGLGLSIVKTLVDLHGGEIAVESLVGVGTTFTVKLPSTDS
>NZ_CP019636.1|WP_087545526.1|7740957_7742859_+|scytonemin-biosynthesis-protein-ScyA
MSENYTQITSQIGDQPYEVYQPNGCVQSEPVGCTHHFEDQPNTHSNTTPVVKEQIQRSLTVADAIAQMMEDLGVNCAFGVNGGAMAGLWGSLSNSLLQVLNFRHEAGAAFAAAEAYFATSRPCVVFTTAGPGITNALTGLFAARGEGAKVILLSACTSSPQRGRWAIQETSTDTLPTEGIFTSGALFNYATTVESAAQLPQIFRKLALGLSQPGGFVAHLSIPTAVQTSPLDDVPLFQGIYCSLVTPDQETIIRTAQLLSEGPFAIWVGFGARSAAKEILQLAERTGAAVMCSPRGKGIFPEDHPQFVGVTGLGGHASVMTYMQQQTPLRTLVLGTRLSEPTSFWNPLLVPPGGFVHVDIDPTVPGVAYSQAETFAIQSDIKAFLQGLLQHDDLLASAAVTAFWLPRPEKEAMQSGPDSPVRPEILLEAIQKVIVQNSDAIVLAECGNSFLWSTHLLQFSQPHRYRISTGVGAMGHAAAGVVGAAVARNGKAVAIVGDGAMLMNNEINTAVKYQIPAVWIVLNDARYNMSYQGMAMLGLKGADALIPEADFAMIARGMGAEGIRINKEDDLEAALEQAMAANGPIVVDVVINADRRAPSKGRNQGLASQGVKSTPVQKTELHMSFPQVSFPNV

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Crispr_ID: NZ_CP019636_29

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019636_29

7786140-7786251

Orphan

Consensus_repeat	Method
AGGGGATGCAGAGGGAGCAGATGAAAA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019636_29

>merge|NZ_CP019636|29|7786140-7786251|CRISPRCasFinder
AGGGGATGCAGAGGGAGCAGATGAAAACAAATCCCATTGTTATTCAACGACTTCTTCCACTGTCGAGGATGGTGTGGAGGGTGGTAGGGGAGGCAGAGGGAGCAGATGAAAA

>NZ_CP019636|29|27|7786140-7786251|CRISPRCasFinder
AGGGGATGCAGAGGGAGCAGATGAAAA	CAAATCCCATTGTTATTCAACGACTTCTTCCACTGTCGAGGATGGTGTGGAGGGTGGT
AGGGGAGGCAGAGGGAGCAGATGAAAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019636.1\|WP_087545617.1\|7771569_7773306_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546483.1\|7796067_7797384_+\|collagen-like-protein	unknown	unknown	gnl\|CDD\|189968
NZ_CP019636.1\|WP_087545650.1\|7779570_7781151_-\|B12-binding-domain-containing-radical-SAM-protein	unknown	unknown	gnl\|CDD\|379101
NZ_CP019636.1\|WP_087545701.1\|7792568_7792871_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087545712.1\|7793613_7794198_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087545672.1\|7783954_7785415_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|315987
NZ_CP019636.1\|WP_087545709.1\|7793143_7793542_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087538405.1\|7788453_7789425_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|225806
NZ_CP019636.1\|WP_087538406.1\|7791069_7791633_-\|recombinase-family-protein	unknown	unknown	gnl\|CDD\|239737
NZ_CP019636.1\|WP_087545626.1\|7776418_7777165_-\|DUF429-domain-containing-protein	unknown	unknown	gnl\|CDD\|226778
NZ_CP019636.1\|WP_087545667.1\|7783420_7783840_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087545694.1\|7791947_7792370_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_157679703.1\|7779423_7779585_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087545656.1\|7781519_7782959_+\|tyrosine-type-recombinase/integrase	unknown	unknown	gnl\|CDD\|271189
NZ_CP019636.1\|WP_087545714.1\|7794272_7795103_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087546137.1\|7789414_7791058_-\|DDE-type-integrase/transposase/recombinase	unknown	unknown	gnl\|CDD\|366234
NZ_CP019636.1\|WP_087545717.1\|7797426_7801164_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|238121
NZ_CP019636.1\|WP_087545623.1\|7773791_7776368_+\|alpha-glucan-family-phosphorylase	unknown	unknown	gnl\|CDD\|340852
NZ_CP019636.1\|WP_087545632.1\|7777529_7778702_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019636.1\|WP_087545642.1\|7779013_7779421_+\|transcriptional-regulator	unknown	unknown	gnl\|CDD\|227786

Protein	Function_ID	Function_description	E-value
NZ_CP019636.1\|WP_087545717.1\|7797426_7801164_-\|AAA-family-ATPase	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.	1.75451e-83
NZ_CP019636.1\|WP_087545656.1\|7781519_7782959_+\|tyrosine-type-recombinase/integrase	gnl\|CDD\|271189	cd01189, INT_ICEBs1_C_like, C-terminal catalytic domain of integrases from bacterial phages and conjugate transposons. This family of tyrosine based site-specific integrases is has origins in bacterial phages and conjugate transposons. One member is the integrase from Bacillus subtilis conjugative transposon ICEBs1. ICEBs1 can be excised and transfered to various recipients in response to DNA damage or high concentrations of potential mating partners. The family belongs to the superfamily of DNA breaking-rejoining enzymes, which share the same fold in their catalytic domain and the overall reaction mechanism. The catalytic domain contains six conserved active site residues. Their overall reaction mechanism involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA.	1.67284e-12
NZ_CP019636.1\|WP_087546483.1\|7796067_7797384_+\|collagen-like-protein	gnl\|CDD\|189968	pfam01391, Collagen, Collagen triple helix repeat (20 copies). Members of this family belong to the collagen superfamily. Collagens are generally extracellular structural proteins involved in formation of connective tissue structure. The alignment contains 20 copies of the G-X-Y repeat that forms a triple helix. The first position of the repeat is glycine, the second and third positions can be any residue but are frequently proline and hydroxy-proline. Collagens are post translationally modified by proline hydroxylase to form the hydroxy-proline residues. Defective hydroxylation is the cause of scurvy. Some members of the collagen superfamily are not involved in connective tissue structure but share the same triple helical structure. The family includes bacterial collagen-like triple-helix repeat proteins.	3.46487e-13
NZ_CP019636.1\|WP_087546137.1\|7789414_7791058_-\|DDE-type-integrase/transposase/recombinase	gnl\|CDD\|366234	pfam00665, rve, Integrase core domain. Integrase mediates integration of a DNA copy of the viral genome into the host chromosome. Integrase is composed of three domains. The amino-terminal domain is a zinc binding domain pfam02022. This domain is the central catalytic domain. The carboxyl terminal domain that is a non-specific DNA binding domain pfam00552. The catalytic domain acts as an endonuclease when two nucleotides are removed from the 3' ends of the blunt-ended viral DNA made by reverse transcription. This domain also catalyzes the DNA strand transfer reaction of the 3' ends of the viral DNA to the 5' ends of the integration site.	1.41381e-07
NZ_CP019636.1\|WP_087538406.1\|7791069_7791633_-\|recombinase-family-protein	gnl\|CDD\|239737	cd03768, SR_ResInv, Serine Recombinase (SR) family, Resolvase and Invertase subfamily, catalytic domain; members contain a C-terminal DNA binding domain. Serine recombinases catalyze site-specific recombination of DNA molecules by a concerted, four-strand cleavage and rejoining mechanism which involves a transient phosphoserine linkage between DNA and the enzyme. They are functionally versatile and include resolvases, invertases, integrases, and transposases. Resolvases and invertases affect resolution or inversion and comprise a major phylogenic group. Resolvases (e.g. Tn3, gamma-delta, and Tn5044) normally recombine two sites in direct repeat causing deletion of the DNA between the sites. Invertases (e.g. Gin and Hin) recombine sites in inverted repeat to invert the DNA between the sites. Cointegrate resolution with gamma-delta resolvase requires the formation of a synaptosome of three resolvase dimers bound to each of two res sites on the DNA. Also included in this subfamily are some putative integrases including a sequence from bacteriophage phi-FC1.	1.3966e-60
NZ_CP019636.1\|WP_087545672.1\|7783954_7785415_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|315987	pfam13424, TPR_12, Tetratricopeptide repeat.	4.56438e-12
NZ_CP019636.1\|WP_087545623.1\|7773791_7776368_+\|alpha-glucan-family-phosphorylase	gnl\|CDD\|340852	cd04299, GT35_Glycogen_Phosphorylase-like, proteins similar to glycogen phosphorylase. This family is most closely related to the oligosaccharide phosphorylase domain family and other unidentified sequences. Oligosaccharide phosphorylase catalyzes the breakdown of oligosaccharides into glucose-1-phosphate units. They are important allosteric enzymes in carbohydrate metabolism.	0
NZ_CP019636.1\|WP_087538405.1\|7788453_7789425_-\|AAA-family-ATPase	gnl\|CDD\|225806	COG3267, ExeA, Type II secretory pathway, component ExeA (predicted ATPase) [Intracellular trafficking and secretion].	3.78807e-53
NZ_CP019636.1\|WP_087545650.1\|7779570_7781151_-\|B12-binding-domain-containing-radical-SAM-protein	gnl\|CDD\|379101	pfam13282, DUF4070, Domain of unknown function (DUF4070). This is a bacterial domain often found at the C-terminus of Radical_SAM methylases.	7.77269e-53
NZ_CP019636.1\|WP_087545626.1\|7776418_7777165_-\|DUF429-domain-containing-protein	gnl\|CDD\|226778	COG4328, COG4328, Predicted nuclease (RNAse H fold) [General function prediction only].	1.93294e-117
NZ_CP019636.1\|WP_087545642.1\|7779013_7779421_+\|transcriptional-regulator	gnl\|CDD\|227786	COG5499, COG5499, Predicted transcription regulator containing HTH domain [Transcription].	1.65322e-15

>NZ_CP019636.1|WP_087545672.1|7783954_7785415_+|tetratricopeptide-repeat-protein
MQQPGTVAISAVAGMGGVGKTELALRYAKQHEADYPGGICWLSARETNLAALIVQFAQLQMNLEVPQELGGKQLTLAQQVNWCWQNWQPPEGLALVVLDDVTDLGNYREFLPTANRFRVLITTRLRNLDTNIEEIPLDVLLPEEALQLLTALVGEKRVQREEETAKELCEWLGYLPLGLELVGRYIAKKPPNWTLAKMLERLKAQRLEDEAIDRHQLQQTLSTAQLGVKAAFELSWLDLHPMTQRVAQLLSLFAPNIFAWKSVESATKTLNWTASDAETANQQLYERHLIQWVEDTEDGYKIHPLIREFLKVKLATSEQVDELKRAFAETLIAIAKTIPNSPTQEFIKSVKNAIPHLAEVAQNLIDAVSDENLPWAFVGLSRFYEGQGLYALAQPWLEQCVSVVQLRLGDEHPDVATSFHNLATLYHSQGRYSEAEPLYIQALEIYEHRLGVNHPHTIISRKNLEGLRSVRGHRAKTGKLYLKRFR
>NZ_CP019636.1|WP_087545667.1|7783420_7783840_+|hypothetical-protein
MEPLTAGAIATLAFKTAFGETIKNLTQATLAKINELRKKIWDKFRGNLQAETALVEAEKGSETSLERVAEYLQELMAKQPEFAADIEKLAREIQQEINIGNIQGQNVQNVYGGKAEQNNANNTNAPVIQGGSGHTITFN
>NZ_CP019636.1|WP_087545656.1|7781519_7782959_+|tyrosine-type-recombinase/integrase
MTYARTPSDKSSKGSIGIQAEQGRLKANFPRQYFGGRQVRKGLSLPDTPEGHAKANLVVRHLQLDLEQGKLNDGYGNFNEIRFQEILCEHGIKANLRVIKGGTARASDQLPPKPELSILEIWDMYCEYKKSNLAITTYENEYCTVYRNYFINAIKSVGEDSIAMRNWLLANRSQSITKKALSALSKAYAMAIRQRLILHNPFDGLCDDIETARRKKVINQADEIEDDSDILNKSKSFTWEEAEEILNYIQSRKKTRHWYSFIKFKFLTGCRTGEAIAFWWCDVKWNEECIIIRRNYSRACKVFKPTKNETNRIFPMPKNGELWNLLKSIPEGQPNECVFKSKQGKIINSAVLSVAWGGSEKYKMQGIIPYLVKEGKVNKYLPCYNTRHTFITHQIFDLGRDEKIVNAWCEHSEETSKKHYQDIMAKAIQTNPDLPNNQQTEIITSEVDSLKKIIKSLQDQLKVQSELIAKLQLQVKQQK
>NZ_CP019636.1|WP_087545650.1|7779570_7781151_-|B12-binding-domain-containing-radical-SAM-protein
MKALLLWPIMPNSFWSYQETLDLAGLRATNPPLGLITVAAMLPADWEIRLVDRNVRLETDDDWAWCDLVMISAMIIQKQDFWELIQKGVALGKKVAVGGPFPTSVPEFALEAGAQYLILDEGECTIPLFLEALARGEEQGIFRATEKPDVTQTPIPRFDLLDLDAYLAVTVQFSRGCPFQCEFCDIINLFGRKPRTKTPEQMLAELEVLYQMGWRRLIFIVDDNFIGNKRNAKVFLRALIPWMQERNYPFILLTEASLNLAEDDELIDLMVQAGFTMVFMGIETPDVESLQVIHKEQNTRQSLMESCHKITRAGLQIMSGFILGFDGEKPGAGQRIQDFVEETGIPQAHLSLLQALHNTSMWTRLKQEGRLLDELGNYFTFQKSLINFIPTRPMEEIVTEYIKAFWNLYEPLPYLKRTFHHFSMMKGKRPSSKRPFGWHELKLFSAICWRQGFVRSTRFRFWWQILAMALQKPHLFYDYFVALGIGEHFFTFRHEVKAQLEAQLEDWKRHKQAQQEEGNLQLSPIS
>NZ_CP019636.1|WP_157679703.1|7779423_7779585_+|hypothetical-protein
MIVQPESFYRSASTKVDVADGLYVLQQITHPLHLLFELLPTLRKLKMTYLTYR
>NZ_CP019636.1|WP_087545642.1|7779013_7779421_+|transcriptional-regulator
MTSGLKSPSDYYMKLINNFPPRPITNQAELIATQNQINSILDKRNLTQDDRDYLKVLGTLVYDYEQQHEPIPILKGVELLKALLEESSLEPRNLAYIFESESIVLDVINGKHKLTENQIKELAKLFHISPSYFVE
>NZ_CP019636.1|WP_087545632.1|7777529_7778702_+|hypothetical-protein
MNIEEIFQKQTFYLNGEEKKGKVLAVSTHVNRRRVCFQIEGEKQGKWFSESELFGTSSENEVIQNESQQYTHSGKVAKSDISVNKQAEKEKEAKNKAERDIHSLINFVAEMQNAIQYRATKDIETVSRFFEDTQKTMIQSLQTAVKAVGDTSNQACQLLDQATQGSGKLITTLHQTITNLWNRYWLERLIDLIKIVDVEKARNTVSKVKGDYPTLPPSQIAEHLINEKAIWATVTGLIGGIVPVLTTIPVDLFATLPLLVQMVYEISFAYEDDSKAAEKPGEILAIFGLALGAEQLGKLGIGFLLKHSPIPNWGIGASTNVIMFLTVGYATREFYEAKVKGVASPITSVEAYITLEKKIGAYLEEAIAEKSTIEATVIEAVSVKKQIVLS
>NZ_CP019636.1|WP_087545626.1|7776418_7777165_-|DUF429-domain-containing-protein
MKFLGIDLGWKSQPSGLCSLELIDGKLQIQDLDRKESIADILTWIDVCVAPHEPAIIAVDAPTLIPNTTGSRLPDKLTHKYFGKYHAGCYPANLGLPFAERTVKFGLELESRGFAHAPTIEPQKPGRYQIEVFPHPATIHLFNLERILKYKKGRLSDRRLELIQLYTYITEILPSLDPPLCPLRLSGSFLSEIPNTGAALKEVEDKLDSLICAYVAAYWWYWGEQRNLVLGDRTTGYIVIPKSVLHDE
>NZ_CP019636.1|WP_087545623.1|7773791_7776368_+|alpha-glucan-family-phosphorylase
MQPIRTFNVSPSLPQRLEPLRKLAYNLHWDWNVETKDLFRRLDPDLWESSRHNPVLMLGTISQARLLEVVEDEGFLAQMDRAARQLEDYFHERTWYQKQRTGHLSDGKAQECYAYFSAEFGLVDCLPIYSGGLGVLAGDHLKSASDLGLPLVGVGLLYQQGYFAQYLNADGWQQERYPINDFYNMPIHLERNPDGSELRIAVDYPGRTVYARVWRVQVGTVPLYMLDTNIEPNNPYDHDITDQLYGGDIDMRIHQEIMLGIGGVRMLKALGYNVTAYHMNEGHAAFSALERIRILIQEQGLNYPEAKQVVASSNIFTTHTPVPAGIDLFPPDKVLHYLGYYADVFGLNKDQFLALGRENTGDLSAPFSMAVLALKMATFSNGVAQLHGVVSRQMFKGLWQNVPTEEVPIKAITNGVHARSCVAKSTQELYDRYLGPSWSSAPPDNPLWERMDAIPDEELWRNHERCRLDMVLYVRERLVKHLHDRGASPSEIAQAQEVLDPNVLTIGFARRFATYKRATLWMRDVERIKRILLGNKDRKVQFVISGKAHPKDIPGKELIRDINHFIREQGLEKQIVFVPNYDIYIARLMVAGCDVWLNTPRRPREASGTSGMKAAMNGLPNLSVLDGWWDEADYVRTGWAIGHGEMYDDPNYQDEIEANAFYDLLEKEVTPLFYDRDVDGLPRHWIDKMKDAIRLNCPFFNTARMVREYAQRAYFPASDRFHTLTADNYAPAKELAAWKENLNAHWYDIKIKDVNVSSGADIEVSQLVNVKAKVDLATLTNDDVRVELYQGAIDANGEIVNGVPVVMDYQGEEQNGLSIYTADIVYNTSGLQGLSLRVLPNHKDLSSPYEPRLIVWAQ
>NZ_CP019636.1|WP_087545617.1|7771569_7773306_+|hypothetical-protein
METSTTIESSSLSQINDDSNSLSSSISFSGGSDNSSAEAKSNQSTSLGNVIIGNGQWIIGEDNTPEQFSSLITDFVTRKLDSVISKLRMRLPLSNAGNPSENGNPFADSRNPFGAGNMPDLPALDSSKSVSGENFPNGVVNPIATGDNQAGDSEHSFADVDLAIVTGDNQAGDSEHSFADVDLAIANGENPIADSSNPFPGGDNPFSGADNTPEQSSFDISKIALGNNNGTDVSGTDVSGEGSTPQIPEVLKSVQDNILSITSSVEDLFANGNTTPLQNPSELLRLFRADMYSFNQGVNTVTKLDSDDSSANVTNLFVSLFAGSDSSASGSNPFGNLLDGNQGQIPFDIITVALEGILPFTGSDNVFTTPDGEIPIGYGNHDFGNGNVAIGNANWNYGNFNASIGNGNWHWDFNKDNATIGNGNWHLDFSENNRTVGNGNWYWESTSDNKTLGNGNWHFGNNNTTIGNGNWDFGSNNTIIGNGNWVFTSNSIVIGNGNWSVIIDKSSNVASDFHGLLDNLELSIGTKDAADNLVNSLLGKFGDAFQPLTGDFDESTLKTYNQLLYSDSNSTTAALPSA
>NZ_CP019636.1|WP_087538405.1|7788453_7789425_-|AAA-family-ATPase
MLTEVMEFYGLVKEFRRAGYYETDHLRQLFKEIKAAIPQGKMIAVTGVVGCGKTVTLRRLQEALKKEGKILVSKSLSVDKNRATLPTLIAALFYDLSSDKEVKISTQGEKRERELQELIRKGKKPVALFVDEAHDLHSSTLTGLKRLIEVVEDSGGILSIILAGHPKLKNDLRRPMMEEIGYRTVIFSLDSIGGSQRQYIEWLLSSCTKEGTLLENLITAEAIDLLCTRLRTPLQIEMHLSLSFEEAHRMGEAIVTLSIVESILSKQIDDLEPTLTRHGYNVKSLSEQLNAKPSEIRSLLRGQLDPTRTRELQEQMLAAGLPI
>NZ_CP019636.1|WP_087546137.1|7789414_7791058_-|DDE-type-integrase/transposase/recombinase
MPNDALVQLRQRLELFPPRSRERRKLIEEAATSYGVSLDTVYRALRERSRPKAEGRSDRGTPRKLSTAEMERYCEIIAAFKIRTSNKKGRHVSTARAIQLLEEYGMETPDGFVQPPAGLLTKSSVNYYLKTWGYDHTSMTRQPPAVRFQADMSNDCWHFDLSPSDLKHLDLPTWIQPGRGNPQLMLYSVVDDRSGVCYQEYHCVYGEDVEAALRFLFNAMSAKTIEGFGFQGIPQMLYTDNGPISKSRVFQNVMECLGVKLVTHLPNGKDGRRVTARAKGKVERPFRTVKEAHETLYHFHQPQTEQEANRWLHQYLLHYNNQPHRQENHSRLEDWLLHLPVKGLQSMCSWERFCTFAREPEQRKVDACARVSVAGVAYEVNPDLAGETVVLWWGLFDNELYVEKDGTKYGPYLPVDGPIPLHRYRKFKKSKTQERADRIAALATGLVLPRAALEGNRELQFLAPSQPKSEPIIIPFQDPDPFQEFTYPSILAAKRAIADNLALPLARLSEQERAFIDELLAQTLSKKVILERVRHYFKQRRENKDAD
>NZ_CP019636.1|WP_087538406.1|7791069_7791633_-|recombinase-family-protein
MLIGYARVSTDDQNLNLQKDALKQAGCSRIYEDRLSGAGVARPGLTKALEAARAGDVLVVWRLDRLGRSLKDLIQMVETLSERGIELHSLTEALATTSTSGKLIFHLFGALAEFERNLIRERTQAGLTAARARGRKGGRPKALDAPKRQLAIKLYNERQYTIEEICRIMGISKPTLYSYIAKAQGTP
>NZ_CP019636.1|WP_087545694.1|7791947_7792370_-|hypothetical-protein
MNTSILNSSEIQNTQTSHGLQPVTKNEPCRHCGKPDWCYRLGNLEVCKRDALAEGWHKTSKADHEGSYYLALTELHKPVRSKQKREWIYNDRNGNPLVKVVRRDDGKGKKKIWQERYENGSWVKGLGNIKRENIPVYRYL
>NZ_CP019636.1|WP_087545701.1|7792568_7792871_-|hypothetical-protein
MELEQDKVVSWKEILGNPYRYGLNSQMLLPNGYKHKGMLRVVGQRKSDDKIPATVCFDEDYVVSFLIKYVFEKLLPESYNDFQKIVSKAYKVWKSQQADK
>NZ_CP019636.1|WP_087545709.1|7793143_7793542_-|hypothetical-protein
MTIITDSLGSWEQIGEIAVTDNWQLFDNPILNSKTFRLTFRTNWEIWGAYNTYQSYGLLRLYYPTAEVTVSNCMRLYVAQEHKILTLSFDPITDTFDIGVKRVIYAKSYYKAPINPDDSLTWYLKLEAKVIT
>NZ_CP019636.1|WP_087545712.1|7793613_7794198_-|hypothetical-protein
MNPKVGVIMGRRVKDSYEIQRILDKAKKREQYREQHRINNPKPYKKRADFRPVYYRDIVDNEKIIKLQASEAAIQKIGDLATVGLLNALPAGKEPISVRGLNYPIVKIMWFYGDDNPVASTTPWGTRVIRYHDKDGAQSHYSIPISSTKVPFGIDDLVSEFQSLFNPNNGTKRALLGARGQAKLVLGRSTILTL
>NZ_CP019636.1|WP_087545714.1|7794272_7795103_-|hypothetical-protein
MTSTPQFNDVELFQQFCLRYVNKRVREYFHDIDDVSIDGLDIDNARQVARAVCLHKDNDPITLTTSRLIAFFIVLGDALDKNPVYSIPTITFQQERKFKPQIQLCFIEDPDDVEPGYSPVAGEISFRLAHESTTTLTNAELVNYGQKVKTNFGSRGGFVWRKGKTMCSYSDWDRGYQLQLLCRDKSEGKRVIEQVLDIQGHTPDWKKMNVSENEEPAAAYPTVPAQETILGKSRRMARKRPIASVKFQYAIVHIHGVRNPIVLYDRTKTKRNPLVI
>NZ_CP019636.1|WP_087546483.1|7796067_7797384_+|collagen-like-protein
MPGPAGPQGTPGKNGERGPQGLPGPPGSQGTHGKNGERGPQGLPGPQGIPGRDGERGSVGLLGPPGPQGIPGKNGTDGRDGKDGKNGKDAPVDNESKRMLEELNRKVSAIPPLIIAKRDPLTFEETVQATNTGVCRSTQPGGCMSKAFNDLGSDVKGNANTNTGNLLNAINLGANAEQLGILNIINTKLGPELPGGLSGTFGRLWQTLQIDRVLNVLILITTFHNAFMLSNNIAQTLFGAIDNIGQVAGFKWKNEKGDEVGFGGLVSQWTTSFFKSIFGEENFNQMVKTYQSANRMYQATTNMLWSIQSMFDSVRSVTELTANNTGKIGNALKRAGVVFENAFPNMSERVTARTATQAKWDNILSGLQPVENAVSAFSSVTGGTVSIGDNFNQLKEQRKEFEKSKQDGEKAVETLINGEKVAVHLKSDMTEKDVRRND
>NZ_CP019636.1|WP_087545717.1|7797426_7801164_-|AAA-family-ATPase
MSDRGLRDENRSIRIEKDAVSSAIISGNGNKVVIYQYQQERQLPEEKVSTIGEIGPNPYKGLLAFLEVDGDRYFGREKQIEKLWNLFRTLHENTTQPEAPLRLLPILGPSGSGKSSLARAGLIPELARRPLPGKSQARVAVLVPGTHPVEALATVLARVATNDQTPVAKTREFAEELKQTSSNTTDTIIYDGLRRIANVLPEIAVSPLVVLVDQFEEVYSLCDDATERQIFIENLIHAAGDRSGCVSVIITLRSDFLGETQRHPALNQAIAKLGVIVPAMSTEELRQAITKPASNAGHPLEEAVVNLLLKDTEGREGALPLLQFALTRIWDGLKKGVEPVKTLEQIGGVGGALADEAQRIYQSLNEQEKKIAQRVFLGLVQLGEGTSDTRRRTNINSLVSYKDEPEYVKKVIDRFAHPGVRLVTLSSIDGTETAEVTHEALFANWGQMRQWLDSSRSDIRFQRRLDEAARVWNENNRPEGSLWRPPDLDLLREYYEQKSEHITPLQVKFFHASVDAEEEKKQNAIKAEQERIRQRQVLTGVLSIGLVLTTVAAISAYRWQNAERGRIEQAAVLVTNRLSNNPLQGYPVQGMVSAINLVAQSRSPFLNFPNQLIPQTIKDSLFSAVEFSREKNVLKGHQGSARGIAISTDGQTIVSGSEDGTVRMWNRKGQPIGGPFKGHLGHITSVAISTDGQTIVSGGVDNTVRMWNSKGEPIGKPFEGHQSPVTSVAISIDGQTIVSGDDNGTVRMWNHKGQPIGELKGHQGNVYTVAISADGNRIFSGGADGTVRMWSRKGQPEGMFSTQQGAISSIAISTDGQTIVSGGYNNTTVRMWNSKGQPIGQPFEGHQLPISSVAISMDGQTIASGSYDGTVRMWNSKGQPINEPFKGHQRPVRTVAISKDGQIIVSGSDDHTLRMWDSESNFFIKGHQGSARSVAISTDGQTIVSGSEDGTVRMWNRKGQPIGGPFKGHLGHITSVAISTDGQTIVSGGVDNTVRMWNSKGEPIGKPFEGHQSPVTSVAISIDGQIIVSGDDNGTVRMWNHKGQPIGELKGHQGNVYTVAISADGNRIFSAGRDGTIRIWNRNGELERKIDTQQGVITSIAISTDGQTIVSGSVDKTVRMWNRKGQPISEPLGHQSPVTSVAISTDGQTIVSGDDDGTVRMWNSKGQPINEPFKGHQRPVRTVAISKDGQIIVSGSDDHTLRMWDMSLDPWLKTACKRLQDHPVFKEPKTPEEKAAKATCEPYLY

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	768954-768978	0	1.0
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	2760803-2760827	0	1.0
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	4220279-4220303	0	1.0
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	5618983-5619007	0	1.0
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	6351180-6351204	0	1.0
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	7778813-7778837	0	1.0
NZ_CP019636_28	28.5\|7726669\|18\|NZ_CP019636\|CRT	7726669-7726686	18	NZ_CP019636.1	7726693-7726710	0	1.0
NZ_CP019636_28	28.5\|7726669\|18\|NZ_CP019636\|CRT	7726669-7726686	18	NZ_CP019636.1	7726705-7726722	0	1.0
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	4056427-4056451	1	0.96
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	4375690-4375714	1	0.96
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	6063192-6063216	1	0.96
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	6257232-6257256	1	0.96
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	6924128-6924152	1	0.96
NZ_CP019636_28	28.3\|7726597\|18\|NZ_CP019636\|CRT	7726597-7726614	18	NZ_CP019636.1	7726472-7726489	1	0.944
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	930955-930979	2	0.92
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	1405237-1405261	2	0.92
NZ_CP019636_1	1.1\|169120\|25\|NZ_CP019636\|CRISPRCasFinder	169120-169144	25	NZ_CP019636.1	4220250-4220274	2	0.92
NZ_CP019636_25	25.1\|7420395\|38\|NZ_CP019636\|CRISPRCasFinder	7420395-7420432	38	NZ_CP019636.1	786934-786971	2	0.947

1. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 768954-768978, mismatch: 0, identity: 1.0

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaatttgtgc	Protospacer
*************************

2. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 2760803-2760827, mismatch: 0, identity: 1.0

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaatttgtgc	Protospacer
*************************

3. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 4220279-4220303, mismatch: 0, identity: 1.0

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaatttgtgc	Protospacer
*************************

4. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 5618983-5619007, mismatch: 0, identity: 1.0

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaatttgtgc	Protospacer
*************************

5. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 6351180-6351204, mismatch: 0, identity: 1.0

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaatttgtgc	Protospacer
*************************

6. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 7778813-7778837, mismatch: 0, identity: 1.0

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaatttgtgc	Protospacer
*************************

7. spacer 28.5|7726669|18|NZ_CP019636|CRT matches to position: 7726693-7726710, mismatch: 0, identity: 1.0

aaacgccacgccaaacgc	CRISPR spacer
aaacgccacgccaaacgc	Protospacer
******************

8. spacer 28.5|7726669|18|NZ_CP019636|CRT matches to position: 7726705-7726722, mismatch: 0, identity: 1.0

aaacgccacgccaaacgc	CRISPR spacer
aaacgccacgccaaacgc	Protospacer
******************

9. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 4056427-4056451, mismatch: 1, identity: 0.96

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaattagtgc	Protospacer
******************** ****

10. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 4375690-4375714, mismatch: 1, identity: 0.96

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaatttatgc	Protospacer
*********************.***

11. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 6063192-6063216, mismatch: 1, identity: 0.96

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaattagtgc	Protospacer
******************** ****

12. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 6257232-6257256, mismatch: 1, identity: 0.96

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaattagtgc	Protospacer
******************** ****

13. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 6924128-6924152, mismatch: 1, identity: 0.96

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgtgacacagctaaatttgtgc	Protospacer
*****.*******************

14. spacer 28.3|7726597|18|NZ_CP019636|CRT matches to position: 7726472-7726489, mismatch: 1, identity: 0.944

tcccgccacgcctcccgc	CRISPR spacer
tcccgccacgcctaccgc	Protospacer
************* ****

15. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 930955-930979, mismatch: 2, identity: 0.92

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgatacagctaaattagtgc	Protospacer
********.*********** ****

16. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 1405237-1405261, mismatch: 2, identity: 0.92

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgagacacagctaaattagtgc	Protospacer
***** ************** ****

17. spacer 1.1|169120|25|NZ_CP019636|CRISPRCasFinder matches to position: 4220250-4220274, mismatch: 2, identity: 0.92

tggcgcgacacagctaaatttgtgc	CRISPR spacer
tggcgcgacacagctaaaatagtgc	Protospacer
****************** * ****

18. spacer 25.1|7420395|38|NZ_CP019636|CRISPRCasFinder matches to position: 786934-786971, mismatch: 2, identity: 0.947

acaggagaagggttttcccgctctcacggcaagactgg	CRISPR spacer
acaggagaaggggtttcccgctctcatggcaagactgg	Protospacer
************ *************.***********

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	MT074142	Bacteroides phage DAC23, complete genome	4973-5003	5	0.839
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	MT074141	Bacteroides phage DAC22, complete genome	6140-6170	5	0.839
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	MT074146	Bacteroides phage SJC03, complete genome	4760-4790	5	0.839
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	MT074139	Bacteroides phage DAC19, complete genome	6140-6170	5	0.839
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	MT074140	Bacteroides phage DAC20, complete genome	6140-6170	5	0.839
NZ_CP019636_8	8.1\|3283779\|27\|NZ_CP019636\|CRISPRCasFinder	3283779-3283805	27	NC_021709	Alteromonas mediterranea 615 plasmid unnamed, complete sequence	73578-73604	5	0.815
NZ_CP019636_10	10.28\|4258268\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4258268-4258301	34	NC_019743	Microcoleus sp. PCC 7113 plasmid pMIC7113.08, complete sequence	17949-17982	6	0.824
NZ_CP019636_27	27.1\|7724058\|31\|NZ_CP019636\|CRISPRCasFinder	7724058-7724088	31	NZ_CP008877	Terribacillus goriensis strain MP602 plasmid pT1, complete sequence	31883-31913	6	0.806
NZ_CP019636_28	28.2\|7726549\|30\|NZ_CP019636\|CRT	7726549-7726578	30	NC_016435	Gordonia phage GRU1, complete genome	58938-58967	6	0.8
NZ_CP019636_28	28.2\|7726549\|30\|NZ_CP019636\|CRT	7726549-7726578	30	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1245012-1245041	6	0.8
NZ_CP019636_28	28.2\|7726549\|30\|NZ_CP019636\|CRT	7726549-7726578	30	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	568058-568087	6	0.8
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	NZ_CP045351	Vibrio sp. THAF100 plasmid pTHAF100_a, complete sequence	592044-592074	7	0.774
NZ_CP019636_10	10.52\|4260006\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260006-4260040	35	NZ_CP015177	Bacillus thuringiensis serovar alesti strain BGSC 4C1 plasmid pBMB267, complete sequence	239601-239635	7	0.8
NZ_CP019636_10	10.52\|4260006\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260006-4260040	35	NZ_CP010090	Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB426, complete sequence	143210-143244	7	0.8
NZ_CP019636_10	10.63\|4260796\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260796-4260829	34	NZ_CP009710	Yersinia pseudotuberculosis IP 32953 strain IP32953 plasmid pYAC_2, complete sequence	8721-8754	7	0.794
NZ_CP019636_10	10.63\|4260796\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260796-4260829	34	NC_006154	Yersinia pseudotuberculosis IP 32953 plasmid pYptb32953, complete sequence	1777-1810	7	0.794
NZ_CP019636_11	11.3\|4554697\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4554697-4554730	34	MT701590	Klebsiella phage Miami, complete genome	140454-140487	7	0.794
NZ_CP019636_28	28.2\|7726549\|30\|NZ_CP019636\|CRT	7726549-7726578	30	NZ_CP046906	Streptomyces sp. QHH-9511 plasmid unnamed, complete sequence	51789-51818	7	0.767
NZ_CP019636_28	28.2\|7726549\|30\|NZ_CP019636\|CRT	7726549-7726578	30	NZ_CP011667	Streptomyces sp. Mg1 plasmid pSMg1-3, complete sequence	90839-90868	7	0.767
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	NZ_CP043858	Arcobacter cibarius strain H743 plasmid pACIB, complete sequence	33745-33775	8	0.742
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	NC_016748	Marinitoga piezophila KA3 plasmid pMARPI01, complete sequence	2391-2421	8	0.742
NZ_CP019636_10	10.52\|4260006\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260006-4260040	35	NZ_CP015592	Bacillus cereus strain AR156 plasmid pAR460, complete sequence	57231-57265	8	0.771
NZ_CP019636_10	10.52\|4260006\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260006-4260040	35	NZ_CP014853	Bacillus thuringiensis strain HD12 plasmid pHD120345, complete sequence	130545-130579	8	0.771
NZ_CP019636_11	11.36\|4557085\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4557085-4557118	34	NZ_CP018784	Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence	525188-525221	8	0.765
NZ_CP019636_13	13.2\|4907651\|35\|NZ_CP019636\|PILER-CR,CRISPRCasFinder,CRT	4907651-4907685	35	NZ_CP050314	Shewanella aestuarii strain PN3F2 plasmid pPN3F2_1, complete sequence	112561-112595	8	0.771
NZ_CP019636_9	9.3\|4115648\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115648-4115681	34	MT080592	UNVERIFIED: Staphylococcus phage vB_SauM_EW3, complete genome	64028-64061	9	0.735
NZ_CP019636_9	9.3\|4115648\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115648-4115681	34	MT080603	UNVERIFIED: Staphylococcus phage vB_SauM_EW9, complete genome	62393-62426	9	0.735
NZ_CP019636_9	9.3\|4115648\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115648-4115681	34	MT080597	UNVERIFIED: Staphylococcus phage vB_SauM_EW5, complete genome	75949-75982	9	0.735
NZ_CP019636_9	9.3\|4115648\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115648-4115681	34	MT080598	UNVERIFIED: Staphylococcus phage vB_SauM_EW6, complete genome	66053-66086	9	0.735
NZ_CP019636_9	9.3\|4115648\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115648-4115681	34	MT080599	UNVERIFIED: Staphylococcus phage vB_SauM_EW7, complete genome	62422-62455	9	0.735
NZ_CP019636_10	10.3\|4256456\|32\|NZ_CP019636\|CRISPRCasFinder,CRT	4256456-4256487	32	NZ_CP007453	Peptoclostridium acidaminophilum DSM 3953 strain al-2 plasmid EAL2_808p, complete sequence	293775-293806	9	0.719
NZ_CP019636_10	10.52\|4260006\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260006-4260040	35	NZ_CP044979	Bacillus thuringiensis strain BT62 plasmid pBT62A, complete sequence	152048-152082	9	0.743
NZ_CP019636_10	10.52\|4260006\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260006-4260040	35	NZ_CP042875	Bacillus cereus strain 09 plasmid unnamed1, complete sequence	489374-489408	9	0.743
NZ_CP019636_10	10.52\|4260006\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4260006-4260040	35	NZ_CP023246	Bacillus cereus strain HBL-AI plasmid unnamed1, complete sequence	241071-241105	9	0.743
NZ_CP019636_11	11.2\|4554626\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4554626-4554659	34	NZ_CP009975	Pseudomonas putida S12 plasmid pTTS12, complete sequence	533263-533296	9	0.735
NZ_CP019636_2	2.1\|1030756\|31\|NZ_CP019636\|CRISPRCasFinder	1030756-1030786	31	MN693779	Marine virus AFVG_250M346, complete genome	55185-55215	10	0.677
NZ_CP019636_9	9.3\|4115648\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115648-4115681	34	NZ_CP043858	Arcobacter cibarius strain H743 plasmid pACIB, complete sequence	18437-18470	10	0.706
NZ_CP019636_9	9.7\|4115934\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115934-4115968	35	NC_019504	Erwinia phage vB_EamM-Y2, complete genome	18229-18263	10	0.714
NZ_CP019636_10	10.4\|4256525\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4256525-4256558	34	KR296684	UNVERIFIED: Salmonella phage 19, complete genome	23158-23191	10	0.706
NZ_CP019636_10	10.4\|4256525\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4256525-4256558	34	NC_029072	Salmonella phage 19, complete genome	23158-23191	10	0.706
NZ_CP019636_11	11.13\|4555422\|35\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4555422-4555456	35	MG945910	UNVERIFIED: Microviridae sp. isolate 6007-1706, partial genome	3438-3472	10	0.714
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP028329	Lactobacillus sp. D1501 plasmid p3, complete sequence	18645-18678	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP032754	Lactobacillus plantarum subsp. argentoratensis strain DSM 16365 plasmid unnamed3, complete sequence	6244-6277	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP015859	Lactobacillus plantarum strain LZ227 plasmid LZ227p4, complete sequence	50862-50895	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP040857	Lactobacillus plantarum strain 202195 plasmid unnamed, complete sequence	35879-35912	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP021675	Lactobacillus brevis strain SRCM101106 plasmid pLB1106-3 sequence	24197-24230	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP017067	Lactobacillus plantarum strain LP3 plasmid pLB301, complete sequence	27383-27416	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP035148	Lactobacillus plantarum strain SRCM103361 plasmid unnamed1	54903-54936	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP035115	Lactobacillus plantarum strain SRCM103295 plasmid unnamed2	227-260	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP035115	Lactobacillus plantarum strain SRCM103295 plasmid unnamed2	61167-61200	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP030245	Lactobacillus plantarum strain Y44 plasmid pY44-1, complete sequence	8204-8237	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP018211	Lactobacillus plantarum strain BLS41 plasmid pLPBLS41_2, complete sequence	20880-20913	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP035567	Lactobacillus plantarum strain SRCM103300 plasmid unnamed1	31959-31992	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP035157	Lactobacillus plantarum strain SRCM103362 plasmid unnamed1	45330-45363	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NC_021912	Lactobacillus plantarum ZJ316 plasmid pLP-ZJ103, complete sequence	40797-40830	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP023774	Lactobacillus plantarum strain PC520 plasmid p2, complete sequence	14474-14507	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP013151	Lactobacillus plantarum strain MF1298 plasmid pMF1298-2, complete sequence	19780-19813	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_AP018409	Lactobacillus plantarum strain SN35N plasmid pSN35N-4, complete sequence	55703-55736	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NC_014558	Lactobacillus plantarum subsp. plantarum ST-III plasmid pST-III, complete sequence	19769-19802	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP032649	Lactobacillus plantarum strain ZFM4 plasmid unnamed1, complete sequence	33765-33798	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP048922	Lactobacillus plantarum strain X7022 plasmid unnamed1, complete sequence	44280-44313	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP048023	Lactobacillus plantarum strain CACC 558 plasmid p1CACC558, complete sequence	29638-29671	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP028277	Lactobacillus plantarum strain SRCM100995 plasmid unnamed2, complete sequence	12992-13025	10	0.706
NZ_CP019636_11	11.26\|4556368\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4556368-4556401	34	NZ_CP028337	Lactobacillus plantarum strain SRCM101167 plasmid unnamed3, complete sequence	11670-11703	10	0.706
NZ_CP019636_11	11.36\|4557085\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4557085-4557118	34	NC_023284	Streptomyces sp. F2 plasmid pFRL4, complete sequence	112003-112036	10	0.706
NZ_CP019636_15	15.2\|4932152\|34\|NZ_CP019636\|PILER-CR,CRT	4932152-4932185	34	NZ_CP033045	Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence	300120-300153	10	0.706
NZ_CP019636_9	9.3\|4115648\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4115648-4115681	34	NZ_CP053316	Bacillus circulans strain GN03 plasmid unnamed, complete sequence	26769-26802	11	0.676
NZ_CP019636_11	11.16\|4555637\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4555637-4555670	34	MN119376	Streptomyces phage Geostin, complete genome	8480-8513	11	0.676
NZ_CP019636_11	11.16\|4555637\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4555637-4555670	34	MH155868	Streptomyces phage FlowerPower, complete genome	8480-8513	11	0.676
NZ_CP019636_11	11.16\|4555637\|34\|NZ_CP019636\|CRISPRCasFinder,CRT,PILER-CR	4555637-4555670	34	MN284894	Streptomyces phage Fabian, complete genome	8480-8513	11	0.676

1. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to MT074142 (Bacteroides phage DAC23, complete genome) position: , mismatch: 5, identity: 0.839

ttctgcataaaatggataatatttgattttg	CRISPR spacer
ctttccataaaatggatagtatttcattttg	Protospacer
.*.* *************.***** ******

2. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to MT074141 (Bacteroides phage DAC22, complete genome) position: , mismatch: 5, identity: 0.839

ttctgcataaaatggataatatttgattttg	CRISPR spacer
ctttccataaaatggataacatttcattttg	Protospacer
.*.* **************.**** ******

3. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to MT074146 (Bacteroides phage SJC03, complete genome) position: , mismatch: 5, identity: 0.839

ttctgcataaaatggataatatttgattttg	CRISPR spacer
ctttccataaaatggataacatttcattttg	Protospacer
.*.* **************.**** ******

4. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to MT074139 (Bacteroides phage DAC19, complete genome) position: , mismatch: 5, identity: 0.839

ttctgcataaaatggataatatttgattttg	CRISPR spacer
ctttccataaaatggatagtatttcattttg	Protospacer
.*.* *************.***** ******

5. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to MT074140 (Bacteroides phage DAC20, complete genome) position: , mismatch: 5, identity: 0.839

ttctgcataaaatggataatatttgattttg	CRISPR spacer
ctttccataaaatggatagtatttcattttg	Protospacer
.*.* *************.***** ******

6. spacer 8.1|3283779|27|NZ_CP019636|CRISPRCasFinder matches to NC_021709 (Alteromonas mediterranea 615 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

gctatttcttggtctttggatgcttga	CRISPR spacer
gctatttcttcgtctttagatgcacca	Protospacer
********** ******.***** . *

7. spacer 10.28|4258268|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NC_019743 (Microcoleus sp. PCC 7113 plasmid pMIC7113.08, complete sequence) position: , mismatch: 6, identity: 0.824

aactcgattcctcctctgttttttgaactgtaat	CRISPR spacer
aactccatccctcctctgttttttgaaagttgat	Protospacer
***** **.******************   *.**

8. spacer 27.1|7724058|31|NZ_CP019636|CRISPRCasFinder matches to NZ_CP008877 (Terribacillus goriensis strain MP602 plasmid pT1, complete sequence) position: , mismatch: 6, identity: 0.806

ttctttgattgagtgcacggctgaagaaaca	CRISPR spacer
tggcgtgattgagtacaaggctgaagaaaca	Protospacer
*  . *********.** *************

9. spacer 28.2|7726549|30|NZ_CP019636|CRT matches to NC_016435 (Gordonia phage GRU1, complete genome) position: , mismatch: 6, identity: 0.8

tcccgccacgcctcccgccacaccaaacgc-	CRISPR spacer
cgccgccacgcctccaggcacacc-aacaca	Protospacer
. ************* * ****** ***.*

10. spacer 28.2|7726549|30|NZ_CP019636|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 6, identity: 0.8

tcccgccacgcctcccgccacaccaaacgc	CRISPR spacer
gcccgccacgcctaccgcctcaccgtgcgc	Protospacer
 ************ ***** ****. .***

11. spacer 28.2|7726549|30|NZ_CP019636|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 6, identity: 0.8

tcccgccacgcctcccgccacaccaaacgc	CRISPR spacer
gcccgccacgcctaccgcctcaccgtgcgc	Protospacer
 ************ ***** ****. .***

12. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to NZ_CP045351 (Vibrio sp. THAF100 plasmid pTHAF100_a, complete sequence) position: , mismatch: 7, identity: 0.774

ttctgcataaaatggataatatttgattttg	CRISPR spacer
atatcagtaaaatgattaatatttgattttg	Protospacer
 * *  .*******. ***************

13. spacer 10.52|4260006|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015177 (Bacillus thuringiensis serovar alesti strain BGSC 4C1 plasmid pBMB267, complete sequence) position: , mismatch: 7, identity: 0.8

tcctttgtgctcgcttattggatctatcctcttgt	CRISPR spacer
ttttttgtgcacgcttaatggatctatccaattct	Protospacer
*..******* ****** ***********  ** *

14. spacer 10.52|4260006|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP010090 (Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB426, complete sequence) position: , mismatch: 7, identity: 0.8

tcctttgtgctcgcttattggatctatcctcttgt	CRISPR spacer
ttttttgtgcacgcttaatggatctatccaattct	Protospacer
*..******* ****** ***********  ** *

15. spacer 10.63|4260796|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009710 (Yersinia pseudotuberculosis IP 32953 strain IP32953 plasmid pYAC_2, complete sequence) position: , mismatch: 7, identity: 0.794

---tgcatcttcaatgtatgcaatattaaatttattt	CRISPR spacer
atatgtattt---atgtattcaatattaaatatattt	Protospacer
   **.**.*   ****** *********** *****

16. spacer 10.63|4260796|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NC_006154 (Yersinia pseudotuberculosis IP 32953 plasmid pYptb32953, complete sequence) position: , mismatch: 7, identity: 0.794

---tgcatcttcaatgtatgcaatattaaatttattt	CRISPR spacer
atatgtattt---atgtattcaatattaaatatattt	Protospacer
   **.**.*   ****** *********** *****

17. spacer 11.3|4554697|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MT701590 (Klebsiella phage Miami, complete genome) position: , mismatch: 7, identity: 0.794

tttgttgtccttcgtttcataatagaaaatggtg	CRISPR spacer
ttctttctttttcgtttcataatcgacaatggtg	Protospacer
**. ** *..************* ** *******

18. spacer 28.2|7726549|30|NZ_CP019636|CRT matches to NZ_CP046906 (Streptomyces sp. QHH-9511 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tcccgccacgcctcccgccacaccaaacgc	CRISPR spacer
acccgccacaccccccgccacacctgccga	Protospacer
 ********.**.*********** . **

19. spacer 28.2|7726549|30|NZ_CP019636|CRT matches to NZ_CP011667 (Streptomyces sp. Mg1 plasmid pSMg1-3, complete sequence) position: , mismatch: 7, identity: 0.767

tcccgccacgcctcccgccacaccaaacgc	CRISPR spacer
ccccgccacacctcccgccccacccctcga	Protospacer
.********.********* ****   **

20. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to NZ_CP043858 (Arcobacter cibarius strain H743 plasmid pACIB, complete sequence) position: , mismatch: 8, identity: 0.742

ttctgcataaaatggataatatttgattttg	CRISPR spacer
tatctcttaaaatagataatattggattttt	Protospacer
* .. * ******.********* ******

21. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to NC_016748 (Marinitoga piezophila KA3 plasmid pMARPI01, complete sequence) position: , mismatch: 8, identity: 0.742

ttctgcataaaatggataatatttgattttg	CRISPR spacer
tttgaaataaaaaagataatatttgatttga	Protospacer
**. . ****** .*************** .

22. spacer 10.52|4260006|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015592 (Bacillus cereus strain AR156 plasmid pAR460, complete sequence) position: , mismatch: 8, identity: 0.771

tcctttgtgctcgcttattggatctatcctcttgt	CRISPR spacer
ttttttgtgcacgcttaatggatctatctaattct	Protospacer
*..******* ****** **********.  ** *

23. spacer 10.52|4260006|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP014853 (Bacillus thuringiensis strain HD12 plasmid pHD120345, complete sequence) position: , mismatch: 8, identity: 0.771

tcctttgtgctcgcttattggatctatcctcttgt	CRISPR spacer
ttttttgtgcacgcttagtggatctatctaattct	Protospacer
*..******* ****** **********.  ** *

24. spacer 11.36|4557085|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018784 (Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence) position: , mismatch: 8, identity: 0.765

cgggtggtacgcgagcagcaggtggaccaattgc	CRISPR spacer
cgggtggttcgggagcagcaggtggcgccgcggc	Protospacer
******** ** *************  * .. **

25. spacer 13.2|4907651|35|NZ_CP019636|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP050314 (Shewanella aestuarii strain PN3F2 plasmid pPN3F2_1, complete sequence) position: , mismatch: 8, identity: 0.771

tcatcatttcagtgtaaacgaacaaaaaagcctgc	CRISPR spacer
acttcatttcagtgtaaacaaacaaaaaagtacca	Protospacer
 * ****************.**********. .

26. spacer 9.3|4115648|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MT080592 (UNVERIFIED: Staphylococcus phage vB_SauM_EW3, complete genome) position: , mismatch: 9, identity: 0.735

tttttcttatttaacaataaatttggaatctgcc-----	CRISPR spacer
tttttagtatttaacaataaatt-----tctgttaatac	Protospacer
*****  ****************     ****..

27. spacer 9.3|4115648|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MT080603 (UNVERIFIED: Staphylococcus phage vB_SauM_EW9, complete genome) position: , mismatch: 9, identity: 0.735

tttttcttatttaacaataaatttggaatctgcc-----	CRISPR spacer
tttttagtatttaacaataaatt-----tctgttaatac	Protospacer
*****  ****************     ****..

28. spacer 9.3|4115648|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MT080597 (UNVERIFIED: Staphylococcus phage vB_SauM_EW5, complete genome) position: , mismatch: 9, identity: 0.735

tttttcttatttaacaataaatttggaatctgcc-----	CRISPR spacer
tttttagtatttaacaataaatt-----tctgttaatac	Protospacer
*****  ****************     ****..

29. spacer 9.3|4115648|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MT080598 (UNVERIFIED: Staphylococcus phage vB_SauM_EW6, complete genome) position: , mismatch: 9, identity: 0.735

tttttcttatttaacaataaatttggaatctgcc-----	CRISPR spacer
tttttagtatttaacaataaatt-----tctgttaatac	Protospacer
*****  ****************     ****..

30. spacer 9.3|4115648|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MT080599 (UNVERIFIED: Staphylococcus phage vB_SauM_EW7, complete genome) position: , mismatch: 9, identity: 0.735

tttttcttatttaacaataaatttggaatctgcc-----	CRISPR spacer
tttttagtatttaacaataaatt-----tctgttaatac	Protospacer
*****  ****************     ****..

31. spacer 10.3|4256456|32|NZ_CP019636|CRISPRCasFinder,CRT matches to NZ_CP007453 (Peptoclostridium acidaminophilum DSM 3953 strain al-2 plasmid EAL2_808p, complete sequence) position: , mismatch: 9, identity: 0.719

agagattaagcttacaaaagcttcatcctcag	CRISPR spacer
tgcatttaagcttacaacaacttcatccggat	Protospacer
 * . ************ *.********  *

32. spacer 10.52|4260006|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP044979 (Bacillus thuringiensis strain BT62 plasmid pBT62A, complete sequence) position: , mismatch: 9, identity: 0.743

tcctttgtgctcgcttattggatctatcctcttgt	CRISPR spacer
atttttgtgcacgcttaatggatctatctaattct	Protospacer
 ..******* ****** **********.  ** *

33. spacer 10.52|4260006|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP042875 (Bacillus cereus strain 09 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.743

tcctttgtgctcgcttattggatctatcctcttgt	CRISPR spacer
atttttgtgcacgcttaatggatctatctaattct	Protospacer
 ..******* ****** **********.  ** *

34. spacer 10.52|4260006|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP023246 (Bacillus cereus strain HBL-AI plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.743

tcctttgtgctcgcttattggatctatcctcttgt	CRISPR spacer
atttttgtgcacgcttaatggatctatctaattct	Protospacer
 ..******* ****** **********.  ** *

35. spacer 11.2|4554626|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009975 (Pseudomonas putida S12 plasmid pTTS12, complete sequence) position: , mismatch: 9, identity: 0.735

ttttgcttgaatgagcgctcttatcttgttgcac	CRISPR spacer
gagttgttgcaggagcgctcttatcttgttgctg	Protospacer
   *  *** * ********************

36. spacer 2.1|1030756|31|NZ_CP019636|CRISPRCasFinder matches to MN693779 (Marine virus AFVG_250M346, complete genome) position: , mismatch: 10, identity: 0.677

ttctgcataaaatggataatatttgattttg	CRISPR spacer
acttgcataaaatgtagaatatttgaaaaga	Protospacer
 ..*********** * *********    .

37. spacer 9.3|4115648|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP043858 (Arcobacter cibarius strain H743 plasmid pACIB, complete sequence) position: , mismatch: 10, identity: 0.706

tttttcttatttaacaataaattt------ggaatctgcc	CRISPR spacer
tttttcttttttaactataaatttttcttaaaaa------	Protospacer
******** ****** ********      ..**

38. spacer 9.7|4115934|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NC_019504 (Erwinia phage vB_EamM-Y2, complete genome) position: , mismatch: 10, identity: 0.714

cattttgtatacgagatttacggcaaactcattct	CRISPR spacer
gctgatgtatacgagattgtcggcaaactcccagt	Protospacer
  *  *************  ********** .  *

39. spacer 10.4|4256525|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to KR296684 (UNVERIFIED: Salmonella phage 19, complete genome) position: , mismatch: 10, identity: 0.706

acgtttgattgactgtgcgagtgtatcatctgtg	CRISPR spacer
gcgtttggttgactgagcgagtgtaaagacacgg	Protospacer
.******.******* *********  . *   *

40. spacer 10.4|4256525|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NC_029072 (Salmonella phage 19, complete genome) position: , mismatch: 10, identity: 0.706

acgtttgattgactgtgcgagtgtatcatctgtg	CRISPR spacer
gcgtttggttgactgagcgagtgtaaagacacgg	Protospacer
.******.******* *********  . *   *

41. spacer 11.13|4555422|35|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MG945910 (UNVERIFIED: Microviridae sp. isolate 6007-1706, partial genome) position: , mismatch: 10, identity: 0.714

tctgaagtacttcagaaataaataatcataataaa	CRISPR spacer
tctgaagtacttcagaaattaagaaaggaagacga	Protospacer
******************* ** **  . *.  .*

42. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP028329 (Lactobacillus sp. D1501 plasmid p3, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

43. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032754 (Lactobacillus plantarum subsp. argentoratensis strain DSM 16365 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

44. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015859 (Lactobacillus plantarum strain LZ227 plasmid LZ227p4, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

45. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP040857 (Lactobacillus plantarum strain 202195 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagttggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

46. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021675 (Lactobacillus brevis strain SRCM101106 plasmid pLB1106-3 sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

47. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017067 (Lactobacillus plantarum strain LP3 plasmid pLB301, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

48. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP035148 (Lactobacillus plantarum strain SRCM103361 plasmid unnamed1) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

49. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP035115 (Lactobacillus plantarum strain SRCM103295 plasmid unnamed2) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

50. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP035115 (Lactobacillus plantarum strain SRCM103295 plasmid unnamed2) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

51. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030245 (Lactobacillus plantarum strain Y44 plasmid pY44-1, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

52. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018211 (Lactobacillus plantarum strain BLS41 plasmid pLPBLS41_2, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

53. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP035567 (Lactobacillus plantarum strain SRCM103300 plasmid unnamed1) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

54. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP035157 (Lactobacillus plantarum strain SRCM103362 plasmid unnamed1) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

55. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NC_021912 (Lactobacillus plantarum ZJ316 plasmid pLP-ZJ103, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

56. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP023774 (Lactobacillus plantarum strain PC520 plasmid p2, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

57. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013151 (Lactobacillus plantarum strain MF1298 plasmid pMF1298-2, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

58. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP018409 (Lactobacillus plantarum strain SN35N plasmid pSN35N-4, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

59. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NC_014558 (Lactobacillus plantarum subsp. plantarum ST-III plasmid pST-III, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

60. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032649 (Lactobacillus plantarum strain ZFM4 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

61. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048922 (Lactobacillus plantarum strain X7022 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

62. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048023 (Lactobacillus plantarum strain CACC 558 plasmid p1CACC558, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

63. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP028277 (Lactobacillus plantarum strain SRCM100995 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

64. spacer 11.26|4556368|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP028337 (Lactobacillus plantarum strain SRCM101167 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.706

tttatgcctcaaacctttctcaagtcatcaaaca	CRISPR spacer
ataagctggcaaatctttctgaagtcatcaaact	Protospacer
 * *  .  ****.****** ************

65. spacer 11.36|4557085|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NC_023284 (Streptomyces sp. F2 plasmid pFRL4, complete sequence) position: , mismatch: 10, identity: 0.706

cgggtggtacgcgagcagcaggtggaccaattgc	CRISPR spacer
tgggtgggacgcgagcagcagctggtgccggacc	Protospacer
.****** ************* ***  * .   *

66. spacer 15.2|4932152|34|NZ_CP019636|PILER-CR,CRT matches to NZ_CP033045 (Bacillus foraminis strain Bac44 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

tccatattttctccttttgtcttcatttttatta	CRISPR spacer
taacagtgccctcgttttgtcttcatttttctta	Protospacer
*    .* ..*** **************** ***

67. spacer 9.3|4115648|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP053316 (Bacillus circulans strain GN03 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.676

tttttcttatttaacaataaatttggaatctgcc	CRISPR spacer
ttttttttatgtaacaataaatttaacgccaatt	Protospacer
*****.**** *************.. ..* ...

68. spacer 11.16|4555637|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MN119376 (Streptomyces phage Geostin, complete genome) position: , mismatch: 11, identity: 0.676

aaaatactgggagtacgtaagagcattgctgtgt	CRISPR spacer
gttccgctggcagtacggaagagcattgctgctc	Protospacer
.   ..**** ****** *************. .

69. spacer 11.16|4555637|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MH155868 (Streptomyces phage FlowerPower, complete genome) position: , mismatch: 11, identity: 0.676

aaaatactgggagtacgtaagagcattgctgtgt	CRISPR spacer
gttccgctggcagtacggaagagcattgctgctc	Protospacer
.   ..**** ****** *************. .

70. spacer 11.16|4555637|34|NZ_CP019636|CRISPRCasFinder,CRT,PILER-CR matches to MN284894 (Streptomyces phage Fabian, complete genome) position: , mismatch: 11, identity: 0.676

aaaatactgggagtacgtaagagcattgctgtgt	CRISPR spacer
gttccgctggcagtacggaagagcattgctgctc	Protospacer
.   ..**** ****** *************. .

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

1085669 : 1190720

Synechococcus_phage(11.11%)

protease,transposase,tail

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_087546001.1\|1085669_1086833_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_157679216.1\|1086835_1086994_+	hypothetical protein	NA	NA	NA	NA
WP_087538328.1\|1087273_1087915_-	hypothetical protein	NA	NA	NA	NA
WP_087538329.1\|1088276_1089473_-\|transposase	IS200/IS605 family element transposase accessory protein TnpB	A0A191SB13	Nostoc_phage	6.1e-111	54.6
WP_087538330.1\|1089708_1090425_-	glycoside hydrolase family protein	I3ULI0	Synechococcus_phage	7.0e-46	57.7
WP_087546004.1\|1090478_1091618_-\|transposase	IS200/IS605 family element transposase accessory protein TnpB	A0A7P9	Microcystis_virus	1.7e-142	65.6
WP_157679219.1\|1091652_1091820_+	CopG family transcriptional regulator	NA	NA	NA	NA
WP_087538331.1\|1091998_1092289_-	hypothetical protein	NA	NA	NA	NA
WP_087538332.1\|1093526_1094205_-\|transposase	IS1 family transposase	NA	NA	NA	NA
WP_087538333.1\|1094909_1096742_+	fatty acyl-AMP ligase	A0A1V0SBX8	Catovirus	2.5e-07	24.4
WP_087538334.1\|1096849_1097122_+	acyl carrier protein	NA	NA	NA	NA
WP_087538335.1\|1097264_1098521_+\|transposase	ISAs1 family transposase	NA	NA	NA	NA
WP_157679710.1\|1098673_1099993_+	hypothetical protein	NA	NA	NA	NA
WP_087546009.1\|1100046_1104846_+	type I polyketide synthase	NA	NA	NA	NA
WP_087538336.1\|1104847_1109629_+	type I polyketide synthase	D0R7J2	Paenibacillus_phage	4.4e-35	31.8
WP_087538337.1\|1109722_1112710_+	type I polyketide synthase	D0R7J2	Paenibacillus_phage	2.3e-34	36.2
WP_087538338.1\|1112755_1114624_+	non-ribosomal peptide synthase	NA	NA	NA	NA
WP_087538339.1\|1114662_1115544_+	SDR family NAD(P)-dependent oxidoreductase	NA	NA	NA	NA
WP_087538340.1\|1115582_1116731_+	UDP-N-acetylglucosamine--LPS N-acetylglucosamine transferase	NA	NA	NA	NA
WP_087538341.1\|1116880_1119172_+	NAD-dependent epimerase/dehydratase family protein	NA	NA	NA	NA
WP_087538342.1\|1119316_1120543_+	hypothetical protein	NA	NA	NA	NA
WP_087538343.1\|1120542_1122111_+	MFS transporter	NA	NA	NA	NA
WP_087538344.1\|1122436_1123501_+	NAD-dependent epimerase/dehydratase family protein	A0A0E3I8S3	Synechococcus_phage	1.5e-15	29.3
WP_087546011.1\|1123689_1124097_+	GtrA family protein	NA	NA	NA	NA
WP_087538345.1\|1124183_1125689_+	glycosyltransferase	NA	NA	NA	NA
WP_087538346.1\|1126025_1127774_+	hypothetical protein	NA	NA	NA	NA
WP_087538347.1\|1128008_1130192_+	hypothetical protein	S5WIY5	Leptospira_phage	4.4e-35	27.9
WP_087538348.1\|1131305_1131917_-	hypothetical protein	NA	NA	NA	NA
WP_087538349.1\|1131918_1132473_-	hypothetical protein	NA	NA	NA	NA
WP_087538350.1\|1132435_1132900_-	FHA domain-containing protein	NA	NA	NA	NA
WP_157679222.1\|1132889_1133114_-	hypothetical protein	NA	NA	NA	NA
WP_087538352.1\|1133197_1134550_-	hypothetical protein	NA	NA	NA	NA
WP_087538353.1\|1134550_1138624_+	hypothetical protein	U5PX75	Bacillus_virus	1.3e-08	24.6
WP_157679225.1\|1138667_1138955_-	hypothetical protein	NA	NA	NA	NA
WP_157679711.1\|1138991_1139090_+	hypothetical protein	NA	NA	NA	NA
WP_087538355.1\|1139104_1140490_-	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_087546013.1\|1140533_1141913_-\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
WP_087546015.1\|1142200_1143271_-\|transposase	transposase	NA	NA	NA	NA
WP_087546013.1\|1143909_1145289_+\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
WP_087538356.1\|1145651_1146674_-	hypothetical protein	NA	NA	NA	NA
WP_087538357.1\|1146652_1151878_-\|tail	phage tail tape measure protein	NA	NA	NA	NA
WP_087538358.1\|1152144_1153470_+	ATP-binding protein	NA	NA	NA	NA
WP_087538359.1\|1153435_1154062_+	RloB domain-containing protein	NA	NA	NA	NA
WP_087538360.1\|1154271_1154643_-	hypothetical protein	NA	NA	NA	NA
WP_087538361.1\|1154743_1156345_-	hypothetical protein	A0A1B0XTN6	Freshwater_phage	7.8e-37	27.0
WP_087538362.1\|1156316_1156688_-	hypothetical protein	NA	NA	NA	NA
WP_157679228.1\|1156734_1156887_-	hypothetical protein	NA	NA	NA	NA
WP_087538364.1\|1157469_1158990_+	N-6 DNA methylase	A0A1V0SLK8	Klosneuvirus	1.0e-22	28.8
WP_087538365.1\|1158980_1160300_+	hypothetical protein	E3T4D5	Cafeteria_roenbergensis_virus	2.5e-09	24.2
WP_087538366.1\|1160296_1161715_+	MloB	NA	NA	NA	NA
WP_087538367.1\|1162174_1163797_+	patatin-like phospholipase family protein	A0A1V0SCG0	Catovirus	1.0e-12	26.5
WP_087538368.1\|1163808_1164105_+	hypothetical protein	NA	NA	NA	NA
WP_087538369.1\|1164161_1164992_+	hypothetical protein	NA	NA	NA	NA
WP_087538370.1\|1165086_1165866_-\|transposase	transposase	NA	NA	NA	NA
WP_087538371.1\|1166503_1166716_+	DUF1016 family protein	NA	NA	NA	NA
WP_087538372.1\|1166952_1169295_+	DEAD/DEAH box helicase	A0A097BY72	Enterococcus_phage	1.9e-23	27.0
WP_157679231.1\|1169892_1170447_-	hypothetical protein	NA	NA	NA	NA
WP_157679234.1\|1170443_1170608_-	hypothetical protein	NA	NA	NA	NA
WP_087538375.1\|1170664_1171471_-	hypothetical protein	NA	NA	NA	NA
WP_087538376.1\|1171463_1171940_-	hypothetical protein	NA	NA	NA	NA
WP_087538377.1\|1174897_1175092_-	CopG family transcriptional regulator	NA	NA	NA	NA
WP_087538378.1\|1175090_1176350_+\|transposase	IS200/IS605 family element transposase accessory protein TnpB	I4AZM3	Saccharomonospora_phage	2.2e-34	36.0
WP_087538379.1\|1176367_1176826_-	hypothetical protein	NA	NA	NA	NA
WP_087538380.1\|1176828_1178649_-	hypothetical protein	NA	NA	NA	NA
WP_157679237.1\|1178675_1179290_-	hypothetical protein	NA	NA	NA	NA
WP_087538382.1\|1179363_1179897_-	hypothetical protein	NA	NA	NA	NA
WP_087538383.1\|1179906_1180368_-	hypothetical protein	NA	NA	NA	NA
WP_087538384.1\|1180372_1181515_-	hypothetical protein	NA	NA	NA	NA
WP_087538385.1\|1181523_1182453_-	hypothetical protein	NA	NA	NA	NA
WP_087538386.1\|1182539_1183475_-	hypothetical protein	NA	NA	NA	NA
WP_157679240.1\|1183477_1184158_-	hypothetical protein	NA	NA	NA	NA
WP_087538388.1\|1184154_1185042_-	hypothetical protein	NA	NA	NA	NA
WP_157679243.1\|1185356_1185515_+	hypothetical protein	NA	NA	NA	NA
WP_087538390.1\|1185553_1186132_+	hypothetical protein	A0A1L2BX57	Bacteriophage	2.1e-24	38.8
WP_087538391.1\|1186131_1187031_+	hypothetical protein	NA	NA	NA	NA
WP_087538392.1\|1188137_1188704_-	hypothetical protein	NA	NA	NA	NA
WP_157679246.1\|1189237_1189960_-	hypothetical protein	NA	NA	NA	NA
WP_157679249.1\|1190396_1190720_-\|protease	protease inhibitor I42 family protein	NA	NA	NA	NA

DBSCAN-SWA_2

2189556 : 2321789

Bacillus_phage(21.05%)

bacteriocin,transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_157679343.1\|2189556_2190717_+\|protease	trypsin-like serine protease	NA	NA	NA	NA
WP_087539081.1\|2190975_2191344_+\|transposase	transposase	A0A1L2BWN4	Bacteriophage	8.8e-45	74.6
WP_087539082.1\|2191463_2192663_-	bifunctional phosphopantothenoylcysteine decarboxylase/phosphopantothenate--cysteine ligase CoaBC	A0A1V0S7W6	Shearwaterpox_virus	3.7e-23	35.7
WP_087539083.1\|2192662_2192875_-	DUF2555 domain-containing protein	NA	NA	NA	NA
WP_087539084.1\|2193067_2193700_-	alpha/beta hydrolase	NA	NA	NA	NA
WP_087539085.1\|2193846_2194845_-	alpha/beta hydrolase	NA	NA	NA	NA
WP_087539086.1\|2195121_2196675_+	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	4.8e-84	55.3
WP_087539087.1\|2197202_2197988_-	FHA domain-containing protein	NA	NA	NA	NA
WP_087539088.1\|2198510_2198966_+	GFA family protein	NA	NA	NA	NA
WP_087539089.1\|2198995_2200159_-	phosphoserine transaminase	NA	NA	NA	NA
WP_087546107.1\|2200393_2200912_-	hypothetical protein	NA	NA	NA	NA
WP_087539090.1\|2201138_2201663_-	peptidoglycan-binding protein	A0A219VHE4	Ochrobactrum_phage	1.4e-06	44.3
WP_087539091.1\|2202050_2202458_+	hypothetical protein	NA	NA	NA	NA
WP_087539092.1\|2202544_2203231_+	hypothetical protein	NA	NA	NA	NA
WP_087546108.1\|2203512_2203944_-	hypothetical protein	NA	NA	NA	NA
WP_087539093.1\|2204362_2204983_+	DUF3611 family protein	NA	NA	NA	NA
WP_087539094.1\|2204983_2205754_-	SDR family oxidoreductase	NA	NA	NA	NA
WP_087539095.1\|2206696_2207074_-	type II toxin-antitoxin system VapC family toxin	NA	NA	NA	NA
WP_087539096.1\|2207063_2207288_-	hypothetical protein	NA	NA	NA	NA
WP_087539097.1\|2207571_2207790_-	toxin-antitoxin system HicB family antitoxin	NA	NA	NA	NA
WP_087539098.1\|2207796_2208219_-	putative toxin-antitoxin system toxin component, PIN family	NA	NA	NA	NA
WP_087539099.1\|2208788_2209187_+	PIN domain-containing protein	NA	NA	NA	NA
WP_087546109.1\|2210111_2210735_+	GUN4 domain-containing protein	NA	NA	NA	NA
WP_087539100.1\|2211001_2212420_+	hypothetical protein	NA	NA	NA	NA
WP_087539101.1\|2213065_2213335_+	BrnT family toxin	NA	NA	NA	NA
WP_087539102.1\|2213324_2213564_+	CopG family transcriptional regulator	NA	NA	NA	NA
WP_087539103.1\|2218183_2220982_-	cadmium-translocating P-type ATPase	E4ZFI9	Streptococcus_phage	4.1e-142	40.7
WP_087539104.1\|2221115_2221520_+	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_087539105.1\|2222339_2223506_-	hypothetical protein	NA	NA	NA	NA
WP_087539107.1\|2223833_2224025_-	CbtB-domain containing protein	NA	NA	NA	NA
WP_087539108.1\|2224242_2224575_-	YnfA family protein	A0A218MNG8	uncultured_virus	2.7e-13	39.8
WP_087539109.1\|2224821_2226147_+	divalent metal cation transporter	NA	NA	NA	NA
WP_087539110.1\|2226234_2226909_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_087539111.1\|2227132_2227513_+	hypothetical protein	NA	NA	NA	NA
WP_087538477.1\|2229039_2229951_-\|transposase	IS982 family transposase	NA	NA	NA	NA
WP_087539113.1\|2230496_2232179_+	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_087539114.1\|2232211_2233498_+	DUF1822 family protein	NA	NA	NA	NA
WP_087539115.1\|2233722_2236044_+	CHASE2 domain-containing protein	NA	NA	NA	NA
WP_087539116.1\|2236339_2237188_+	DUF928 domain-containing protein	NA	NA	NA	NA
WP_087539117.1\|2237244_2240877_+	filamentous hemagglutinin N-terminal domain-containing protein	NA	NA	NA	NA
WP_087539119.1\|2241352_2241895_+\|transposase	transposase	NA	NA	NA	NA
WP_087546110.1\|2242007_2244944_+\|bacteriocin	NHLP bacteriocin export ABC transporter permease/ATPase subunit	W8CYL7	Bacillus_phage	1.3e-29	25.9
WP_087539120.1\|2245058_2247713_-	S-layer family protein	NA	NA	NA	NA
WP_087539121.1\|2248117_2248339_-	hypothetical protein	NA	NA	NA	NA
WP_087546111.1\|2248596_2250798_-\|bacteriocin	NHLP family bacteriocin export ABC transporter peptidase/permease/ATPase subunit	W8CYL7	Bacillus_phage	3.8e-34	25.7
WP_087539122.1\|2250906_2252175_-\|bacteriocin	NHLP bacteriocin system secretion protein	NA	NA	NA	NA
WP_087539123.1\|2252755_2255674_-	CHAT domain-containing protein	NA	NA	NA	NA
WP_087539124.1\|2256127_2256889_+	MinD/ParA family protein	F0PIG8	Enterococcus_phage	5.7e-06	24.2
WP_087539125.1\|2257041_2257986_+	methyl-accepting chemotaxis protein	NA	NA	NA	NA
WP_087539126.1\|2258051_2259161_+	cyclic nucleotide-binding domain-containing protein	NA	NA	NA	NA
WP_087546013.1\|2259603_2260983_+\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
WP_087546112.1\|2261021_2262467_+\|bacteriocin	NHLP bacteriocin system secretion protein	NA	NA	NA	NA
WP_087539127.1\|2262482_2264699_+\|bacteriocin	NHLP family bacteriocin export ABC transporter peptidase/permease/ATPase subunit	W8CYL7	Bacillus_phage	1.7e-37	26.0
WP_087546113.1\|2264741_2267600_+\|bacteriocin	NHLP bacteriocin export ABC transporter permease/ATPase subunit	W8CYL7	Bacillus_phage	3.7e-29	24.2
WP_087539128.1\|2268133_2269714_+	protein kinase	A0A1V0SE45	Indivirus	2.7e-10	26.2
WP_157679345.1\|2270191_2271028_+	hypothetical protein	NA	NA	NA	NA
WP_087539129.1\|2271126_2271435_+	hypothetical protein	NA	NA	NA	NA
WP_157679347.1\|2271939_2273709_+	protein kinase	A0A1V0SBL0	Catovirus	6.4e-08	23.7
WP_087539130.1\|2274443_2278031_+	hypothetical protein	NA	NA	NA	NA
WP_087539131.1\|2278097_2280365_+	TOMM precursor leader peptide-binding protein	NA	NA	NA	NA
WP_087539132.1\|2280498_2281911_+	SagB/ThcOx family dehydrogenase	NA	NA	NA	NA
WP_087539133.1\|2281968_2282289_-	Nif11-like leader peptide family natural product precursor	NA	NA	NA	NA
WP_087539134.1\|2282404_2282731_-	Nif11-like leader peptide family natural product precursor	NA	NA	NA	NA
WP_087539135.1\|2283122_2286371_+	type 2 lantipeptide synthetase LanM	NA	NA	NA	NA
WP_087539136.1\|2286879_2288343_+	hypothetical protein	NA	NA	NA	NA
WP_087539137.1\|2288885_2290178_+\|protease	PrsW family intramembrane metalloprotease	NA	NA	NA	NA
WP_087539138.1\|2291082_2292219_+	hypothetical protein	NA	NA	NA	NA
WP_087539139.1\|2292205_2294014_+	hypothetical protein	NA	NA	NA	NA
WP_087539140.1\|2294199_2295657_+	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_087539141.1\|2295711_2296875_+	hypothetical protein	NA	NA	NA	NA
WP_157679349.1\|2296920_2297133_-	hypothetical protein	NA	NA	NA	NA
WP_087539143.1\|2298481_2299381_+	undecaprenyl-diphosphate phosphatase	NA	NA	NA	NA
WP_087539144.1\|2299680_2303673_+	non-ribosomal peptide synthetase	A0A2K9KZV5	Tupanvirus	2.3e-66	30.8
WP_087539146.1\|2303929_2304727_+	amino acid amidase	NA	NA	NA	NA
WP_087539147.1\|2305005_2308230_-	efflux RND transporter permease subunit	S5VTK5	Leptospira_phage	1.6e-89	24.4
WP_087546114.1\|2308294_2309830_-	efflux RND transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_157679351.1\|2309905_2310370_-	hypothetical protein	NA	NA	NA	NA
WP_087539148.1\|2310701_2311577_+	metal-dependent phosphohydrolase	A0A2I2L3U5	Orpheovirus	5.3e-88	58.1
WP_087539149.1\|2311660_2312779_+	ABC transporter permease	NA	NA	NA	NA
WP_087539150.1\|2312879_2315333_-	hypothetical protein	NA	NA	NA	NA
WP_157679353.1\|2316516_2317032_+	hypothetical protein	NA	NA	NA	NA
WP_087539152.1\|2319069_2320395_-	MFS transporter	A0A2K5B2B5	Erysipelothrix_phage	3.2e-28	29.4
WP_087539153.1\|2321102_2321789_+\|transposase	IS1 family transposase	A0A218MNG1	uncultured_virus	4.2e-08	33.1

DBSCAN-SWA_3

2842879 : 2879340

Wolbachia_phage(25.0%)

integrase,transposase

attL 2833963:2834022|attR 2880456:2881630

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
2833963:2834022	attL	NA	NA	NA	NA
WP_087539735.1\|2842879_2843122_+\|transposase	transposase	NA	NA	NA	NA
WP_087546013.1\|2843101_2844481_-\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
WP_157679407.1\|2846577_2846844_+	hypothetical protein	NA	NA	NA	NA
WP_157679409.1\|2847790_2847970_+	hypothetical protein	NA	NA	NA	NA
WP_087539745.1\|2848196_2848628_+	hypothetical protein	NA	NA	NA	NA
WP_157679411.1\|2849109_2849604_-	hypothetical protein	NA	NA	NA	NA
WP_157679413.1\|2850461_2850632_+	ssl1498 family light-harvesting-like protein	NA	NA	NA	NA
WP_087546135.1\|2851232_2851526_+	plasmid maintenance system killer protein	NA	NA	NA	NA
WP_087539751.1\|2851548_2851848_+	HigA family addiction module antidote protein	B0VK57	Azospirillum_phage	2.3e-11	45.9
WP_157679415.1\|2852164_2853250_+	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_087539754.1\|2853255_2853522_-	hypothetical protein	NA	NA	NA	NA
WP_087539757.1\|2853569_2853953_-	hypothetical protein	NA	NA	NA	NA
WP_087539759.1\|2854017_2854296_-	hypothetical protein	NA	NA	NA	NA
WP_087539761.1\|2854549_2854903_+	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_087539763.1\|2854964_2856194_+	hypothetical protein	A0A0U4JX08	Bacillus_phage	1.6e-13	36.5
WP_087539765.1\|2856170_2858582_-	NACHT domain-containing NTPase	NA	NA	NA	NA
WP_087539767.1\|2858738_2859014_+	hypothetical protein	NA	NA	NA	NA
WP_157679417.1\|2859216_2859477_+	hypothetical protein	NA	NA	NA	NA
WP_087546015.1\|2859811_2860882_+\|transposase	transposase	NA	NA	NA	NA
WP_087546013.1\|2861169_2862549_+\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
WP_157679419.1\|2862538_2862958_+	hypothetical protein	NA	NA	NA	NA
WP_087539773.1\|2862985_2863267_-	hypothetical protein	NA	NA	NA	NA
WP_087539775.1\|2863592_2863814_-	addiction module protein	NA	NA	NA	NA
WP_087539777.1\|2864107_2865040_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_087539779.1\|2865140_2865596_-	hypothetical protein	NA	NA	NA	NA
WP_087539782.1\|2865892_2866303_+	nuclear transport factor 2 family protein	NA	NA	NA	NA
WP_087539784.1\|2866502_2869757_-	DEAD/DEAH box helicase	A0A2H4J643	uncultured_Caudovirales_phage	3.9e-27	25.1
WP_087539786.1\|2869777_2870260_-	DUF3368 domain-containing protein	NA	NA	NA	NA
WP_087539788.1\|2870256_2870523_-	UPF0175 family protein	NA	NA	NA	NA
WP_087539790.1\|2870680_2873617_-	DUF1156 domain-containing protein	K9MDJ7	Sulfolobus_virus	3.5e-43	26.5
WP_087546136.1\|2873628_2874072_-	hypothetical protein	NA	NA	NA	NA
WP_087539792.1\|2874138_2875998_-	hypothetical protein	NA	NA	NA	NA
WP_087539794.1\|2875993_2876842_+	ATP-binding cassette domain-containing protein	A0A2H4PQG7	Staphylococcus_phage	1.3e-11	26.6
WP_087538406.1\|2877121_2877685_+	recombinase family protein	I1ZBD6	Salisaeta_icosahedral_phage	3.7e-42	50.3
WP_087546137.1\|2877696_2879340_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	NA	NA	NA	NA
2880456:2881630	attR	NA	NA	NA	NA

DBSCAN-SWA_4

4874874 : 4916967

Wolbachia_phage(60.0%)

integrase,transposase

attL 4877949:4878008|attR 4917210:4918894

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_087546013.1\|4874874_4876254_-\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
WP_087546268.1\|4876892_4877963_+\|transposase	transposase	NA	NA	NA	NA
4877949:4878008	attL	NA	NA	NA	NA
WP_087546013.1\|4878250_4879630_+\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
WP_157679560.1\|4880250_4880802_-	hypothetical protein	NA	NA	NA	NA
WP_087541873.1\|4881147_4881549_-	nitrogen fixation protein NifX	NA	NA	NA	NA
WP_087541874.1\|4881621_4883034_-	nitrogenase iron-molybdenum cofactor biosynthesis protein NifE	NA	NA	NA	NA
WP_087541877.1\|4885681_4886869_+	helix-turn-helix domain-containing protein	A0A1V0E021	Clostridioides_phage	8.9e-06	44.1
WP_087541878.1\|4887335_4888466_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_157679562.1\|4888826_4888982_+	hypothetical protein	NA	NA	NA	NA
WP_087541879.1\|4890152_4891109_-\|transposase	transposase	NA	NA	NA	NA
WP_087541880.1\|4891859_4892159_-	2Fe-2S iron-sulfur cluster binding domain-containing protein	A0A222YX16	Synechococcus_phage	2.0e-23	56.5
WP_087541881.1\|4892347_4892716_-	iron-sulfur cluster assembly accessory protein	NA	NA	NA	NA
WP_087541882.1\|4892738_4892957_-	hypothetical protein	NA	NA	NA	NA
WP_087541883.1\|4892980_4893778_-	HesA/MoeB/ThiF family protein	NA	NA	NA	NA
WP_087541884.1\|4893788_4894106_-	nitrogenase-stabilizing/protective protein NifW	NA	NA	NA	NA
WP_087546269.1\|4894102_4894324_-	hypothetical protein	NA	NA	NA	NA
WP_087541885.1\|4894411_4894888_-	NifX-associated nitrogen fixation protein	NA	NA	NA	NA
WP_087541886.1\|4894884_4895298_-	nitrogen fixation protein NifX	NA	NA	NA	NA
WP_087541887.1\|4895397_4896744_-	nitrogenase iron-molybdenum cofactor biosynthesis protein NifN	NA	NA	NA	NA
WP_087541888.1\|4896743_4898267_-	nitrogenase iron-molybdenum cofactor biosynthesis protein NifE	NA	NA	NA	NA
WP_087541889.1\|4898517_4898844_-	nitrogenase	NA	NA	NA	NA
WP_087541890.1\|4899066_4900602_-	nitrogenase molybdenum-iron protein subunit beta	NA	NA	NA	NA
WP_087541891.1\|4900786_4900882_-	nitrogenase molybdenum-iron protein subunit alpha	NA	NA	NA	NA
WP_087546270.1\|4901172_4902474_+\|integrase	integrase	NA	NA	NA	NA
WP_087541892.1\|4902965_4904066_+	isopenicillin N synthase family oxygenase	NA	NA	NA	NA
WP_087541893.1\|4904570_4905110_-	DUF2267 domain-containing protein	NA	NA	NA	NA
WP_157679564.1\|4905232_4905394_+	hypothetical protein	NA	NA	NA	NA
WP_087541894.1\|4905447_4905930_-	DUF3368 domain-containing protein	NA	NA	NA	NA
WP_087546271.1\|4905913_4906168_-	UPF0175 family protein	NA	NA	NA	NA
WP_087541895.1\|4906203_4906383_-	hypothetical protein	NA	NA	NA	NA
WP_087546272.1\|4906410_4906674_-	hypothetical protein	NA	NA	NA	NA
WP_087541896.1\|4909070_4910186_+	CRISPR-associated endoribonuclease Cas6	NA	NA	NA	NA
WP_087541897.1\|4910214_4910721_-	hypothetical protein	NA	NA	NA	NA
WP_087541898.1\|4910899_4911544_-	hypothetical protein	NA	NA	NA	NA
WP_087541899.1\|4911546_4912587_-	CRISPR-associated protein	NA	NA	NA	NA
WP_087541900.1\|4912583_4913144_-	hypothetical protein	NA	NA	NA	NA
WP_087541901.1\|4913140_4914154_-	CRISPR-associated protein	NA	NA	NA	NA
WP_087541902.1\|4914184_4914805_-	hypothetical protein	NA	NA	NA	NA
WP_087541903.1\|4914806_4915613_-	CRISPR-associated RAMP protein	NA	NA	NA	NA
WP_087546013.1\|4915587_4916967_-\|transposase	IS110 family transposase	Q9JMN8	Wolbachia_phage	1.5e-142	57.2
4917210:4918894	attR	NA	NA	NA	NA

DBSCAN-SWA_5

6541460 : 6624965

Bacillus_virus(36.36%)

tRNA,transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_087543480.1\|6541460_6542180_+\|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA
WP_087543482.1\|6542323_6542995_+\|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA
WP_087543484.1\|6543249_6544356_+	peptidylprolyl isomerase	NA	NA	NA	NA
WP_087543486.1\|6544711_6546589_+	excinuclease ABC subunit UvrC	NA	NA	NA	NA
WP_157679668.1\|6546633_6546873_+	hypothetical protein	NA	NA	NA	NA
WP_087546396.1\|6548395_6548575_+	replication restart DNA helicase PriA	NA	NA	NA	NA
WP_087543488.1\|6548674_6549766_-	23S rRNA (adenine(2503)-C(2))-methyltransferase RlmN	NA	NA	NA	NA
WP_087543490.1\|6549856_6550186_-	methyltransferase	NA	NA	NA	NA
WP_087543492.1\|6550207_6550561_-	hypothetical protein	NA	NA	NA	NA
WP_087543494.1\|6550697_6551486_-	precorrin-4 C(11)-methyltransferase	NA	NA	NA	NA
WP_087543496.1\|6551670_6552522_-	prolipoprotein diacylglyceryl transferase	NA	NA	NA	NA
WP_087543498.1\|6552929_6553496_+	pantetheine-phosphate adenylyltransferase	A0A1B1IVQ3	uncultured_Mediterranean_phage	5.9e-24	43.0
WP_087543500.1\|6553537_6554083_+	hypothetical protein	NA	NA	NA	NA
WP_087543502.1\|6554439_6556101_+\|protease	M48 family metalloprotease	NA	NA	NA	NA
WP_087546397.1\|6556172_6556982_+	hypothetical protein	NA	NA	NA	NA
WP_087543507.1\|6559031_6562628_+	phytase	NA	NA	NA	NA
WP_087543509.1\|6562817_6563858_-	DUF1611 domain-containing protein	NA	NA	NA	NA
WP_087543511.1\|6563841_6564894_-	dipeptide epimerase	NA	NA	NA	NA
WP_087543513.1\|6565156_6565705_+	NUDIX hydrolase	NA	NA	NA	NA
WP_087543516.1\|6565819_6566743_-	nucleoside hydrolase	NA	NA	NA	NA
WP_087543518.1\|6566756_6567188_+	nucleoside deaminase	F4YXM7	Roseobacter_phage	6.1e-05	51.1
WP_087543520.1\|6567261_6568188_-	ribokinase	NA	NA	NA	NA
WP_087543522.1\|6568424_6568982_-	sugar O-acetyltransferase	NA	NA	NA	NA
WP_087543524.1\|6569038_6570346_-	diguanylate cyclase	G3MA91	Bacillus_virus	3.7e-29	38.8
WP_087543526.1\|6571029_6571398_-	dihydroneopterin aldolase	NA	NA	NA	NA
WP_087543528.1\|6571573_6573352_+	2-succinyl-5-enolpyruvyl-6-hydroxy-3- cyclohexene-1-carboxylic-acid synthase	NA	NA	NA	NA
WP_087543530.1\|6573364_6575449_-	S8 family serine peptidase	NA	NA	NA	NA
WP_087543535.1\|6575818_6576613_+	TIGR00297 family protein	NA	NA	NA	NA
WP_087543537.1\|6576799_6577558_+	peptidylprolyl isomerase	NA	NA	NA	NA
WP_087543539.1\|6577506_6580296_+	type I secretion system permease/ATPase	A0A1V0SJ29	Klosneuvirus	7.4e-19	23.4
WP_087543541.1\|6580396_6581266_-	alpha/beta hydrolase	NA	NA	NA	NA
WP_087543543.1\|6581470_6582061_+	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_087543545.1\|6582111_6582543_+	glyoxalase	NA	NA	NA	NA
WP_087543547.1\|6582566_6583268_-	triacylglycerol lipase	NA	NA	NA	NA
WP_087543550.1\|6583706_6584261_+	hypothetical protein	NA	NA	NA	NA
WP_087538489.1\|6584587_6585733_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_087543553.1\|6585813_6586548_-	16S rRNA (uracil(1498)-N(3))-methyltransferase	NA	NA	NA	NA
WP_087543556.1\|6588487_6589144_-	Uma2 family endonuclease	NA	NA	NA	NA
WP_087546398.1\|6589337_6589523_-	hypothetical protein	NA	NA	NA	NA
WP_087543560.1\|6589948_6591028_-	ATP-dependent 6-phosphofructokinase	H8ZJH0	Ostreococcus_tauri_virus	3.3e-07	27.2
WP_087543562.1\|6591689_6593720_-	sulfite reductase, ferredoxin dependent	NA	NA	NA	NA
WP_087543565.1\|6594049_6594595_-	hypothetical protein	NA	NA	NA	NA
WP_087543567.1\|6594837_6595701_-	hypothetical protein	NA	NA	NA	NA
WP_087543570.1\|6596226_6597588_+	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_087543573.1\|6597747_6598587_+	nitrate ABC transporter permease	NA	NA	NA	NA
WP_087543576.1\|6598679_6600686_+	ATP-binding cassette domain-containing protein	G3M9Y6	Bacillus_virus	1.8e-27	37.1
WP_087543579.1\|6600861_6601710_+	ATP-binding cassette domain-containing protein	G3M9Y6	Bacillus_virus	8.0e-33	39.5
WP_087543582.1\|6601868_6602936_-\|transposase	transposase	NA	NA	NA	NA
WP_087543585.1\|6602954_6603836_-	hypothetical protein	NA	NA	NA	NA
WP_087543587.1\|6603950_6604610_-	hypothetical protein	NA	NA	NA	NA
WP_157679669.1\|6605029_6605728_+	hypothetical protein	NA	NA	NA	NA
WP_087543590.1\|6605810_6608651_-	insulinase family protein	G3MBJ8	Bacillus_virus	7.1e-25	25.5
WP_087543593.1\|6608984_6609989_+\|tRNA	tRNA lysidine(34) synthetase TilS	NA	NA	NA	NA
WP_087543596.1\|6612358_6613585_+	response regulator	NA	NA	NA	NA
WP_087543599.1\|6613737_6614103_+	response regulator	W8CYM9	Bacillus_phage	8.2e-19	41.9
WP_087543602.1\|6614116_6614647_+	purine-binding chemotaxis protein CheW	NA	NA	NA	NA
WP_087543605.1\|6614663_6617678_+	HAMP domain-containing protein	A0A2H4J162	uncultured_Caudovirales_phage	1.2e-14	36.6
WP_087543608.1\|6617787_6622728_+	response regulator	NA	NA	NA	NA
WP_087546400.1\|6622860_6623157_-	hypothetical protein	NA	NA	NA	NA
WP_087543611.1\|6623705_6624965_+\|transposase	transposase	A0A191SB13	Nostoc_phage	3.2e-187	77.9

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_CP019636

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection