CRISPRimmunity

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Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP036292	Planctomycetes bacterium CA51 chromosome, complete genome	31 crisprs	RT,cas3,DEDDh,csa3,WYL,DinG	4	4	4	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP036292_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_1

145313-145410

Orphan

Consensus_repeat	Method
TCGCCATGCCGTCGCTTTCGCGACTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_1

>merge|NZ_CP036292|1|145313-145410|CRISPRCasFinder
TCGCCATGCCGTCGCTTTCGCGACTGAGATGCTCCGCTGCGCACCAATTTCCTGGGACTTGCGTCCCAGGCTATCGCATGCCGTCGCTTTCGCGACTG

>NZ_CP036292|1|1|145313-145410|CRISPRCasFinder
TCGCCATGCCGTCGCTTTCGCGACTG	AGATGCTCCGCTGCGCACCAATTTCCTGGGACTTGCGTCCCAGGCT
ATCGCATGCCGTCGCTTTCGCGACTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123940.1\|162642_163395_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|226149
NZ_CP036292.1\|WP_145117195.1\|129992_131033_+\|deoxyribonuclease	unknown	unknown	gnl\|CDD\|197337
NZ_CP036292.1\|WP_145117210.1\|160620_162300_+\|dihydroxy-acid-dehydratase	unknown	unknown	gnl\|CDD\|234861
NZ_CP036292.1\|WP_145117209.1\|159731_160373_-\|DUF1080-domain-containing-protein	unknown	unknown	gnl\|CDD\|368908
NZ_CP036292.1\|WP_145117211.1\|163564_166189_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235906
NZ_CP036292.1\|WP_145117198.1\|134381_135926_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP036292.1\|WP_145117208.1\|153403_159529_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117197.1\|132765_134010_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|380163
NZ_CP036292.1\|WP_145117196.1\|131051_132455_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117205.1\|147466_149782_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|273429
NZ_CP036292.1\|WP_145117202.1\|143902_144994_-\|RluA-family-pseudouridine-synthase	unknown	unknown	gnl\|CDD\|223638
NZ_CP036292.1\|WP_145123939.1\|137622_141288_-\|general-secretion-pathway-protein-GspD	unknown	unknown	gnl\|CDD\|274175
NZ_CP036292.1\|WP_145117194.1\|129410_129938_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117200.1\|136709_137480_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117203.1\|145815_146643_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|370767
NZ_CP036292.1\|WP_145117201.1\|141608_143516_-\|asparagine-synthase-(glutamine-hydrolyzing)	unknown	unknown	gnl\|CDD\|223444
NZ_CP036292.1\|WP_145117207.1\|151759_152827_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117199.1\|135959_136613_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|238141
NZ_CP036292.1\|WP_145117204.1\|146778_147147_-\|DUF2237-family-protein	unknown	unknown	gnl\|CDD\|378344
NZ_CP036292.1\|WP_145117206.1\|149941_151366_-\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|373239

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123940.1\|162642_163395_+\|TIM-barrel-protein	gnl\|CDD\|226149	COG3622, Hfi, Hydroxypyruvate isomerase [Carbohydrate transport and metabolism].	5.27215e-31
NZ_CP036292.1\|WP_145117195.1\|129992_131033_+\|deoxyribonuclease	gnl\|CDD\|197337	cd10282, DNase1, Deoxyribonuclease 1. Deoxyribonuclease 1 (DNase1, EC 3.1.21.1), also known as DNase I, is a Ca2+, Mg2+/Mn2+-dependent secretory endonuclease, first isolated from bovine pancreas extracts. It cleaves DNA preferentially at phosphodiester linkages next to a pyrimidine nucleotide, producing 5'-phosphate terminated polynucleotides with a free hydroxyl group on position 3'. It generally produces tetranucleotides. DNase1 substrates include single-stranded DNA, double-stranded DNA, and chromatin. This enzyme may be responsible for apoptotic DNA fragmentation. Other deoxyribonucleases in this subfamily include human DNL1L (human DNase I lysosomal-like, also known as DNASE1L1, Xib, and DNase X ), human DNASE1L2 (also known as DNAS1L2), and DNASE1L3 (also known as DNAS1L3, nhDNase, LS-DNase, DNase Y, and DNase gamma) . DNASE1L3 is implicated in apoptotic DNA fragmentation. DNase I is also a cytoskeletal protein which binds actin. A recombinant form of human DNase1 is used as a mucoactive therapy in patients with cystic fibrosis; it hydrolyzes the extracellular DNA in sputum and reduces its viscosity. Mutations in the gene encoding DNase1 have been associated with Systemic Lupus Erythematosus, a multifactorial autoimmune disease. This subfamily belongs to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds.	3.04914e-68
NZ_CP036292.1\|WP_145117210.1\|160620_162300_+\|dihydroxy-acid-dehydratase	gnl\|CDD\|234861	PRK00911, PRK00911, dihydroxy-acid dehydratase; Provisional.	0
NZ_CP036292.1\|WP_145117209.1\|159731_160373_-\|DUF1080-domain-containing-protein	gnl\|CDD\|368908	pfam06439, DUF1080, Domain of Unknown Function (DUF1080). This family has structural similarity to an endo-1,3-1,4-beta glucanase belonging to glycoside hydrolase family 16. However, the structure surrounding the active site differs from that of the endo-1,3-1,4-beta glucanase.	3.57705e-49
NZ_CP036292.1\|WP_145117211.1\|163564_166189_+\|hypothetical-protein	gnl\|CDD\|235906	PRK07003, PRK07003, DNA polymerase III subunit gamma/tau.	3.80964e-08
NZ_CP036292.1\|WP_145117198.1\|134381_135926_+\|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.	4.8544e-56
NZ_CP036292.1\|WP_145117197.1\|132765_134010_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|380163	NF033113, halo_ClmS, chloramphenicol-biosynthetic FADH2-dependent halogenase CmlS.	3.76117e-57
NZ_CP036292.1\|WP_145117205.1\|147466_149782_+\|AAA-family-ATPase	gnl\|CDD\|273429	TIGR01073, ATP-dependent_DNA_helicase_PcrA, ATP-dependent DNA helicase PcrA. Designed to identify pcrA members of the uvrD/rep subfamily. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP036292.1\|WP_145117202.1\|143902_144994_-\|RluA-family-pseudouridine-synthase	gnl\|CDD\|223638	COG0564, RluA, Pseudouridylate synthases, 23S RNA-specific [Translation, ribosomal structure and biogenesis].	4.02839e-101
NZ_CP036292.1\|WP_145123939.1\|137622_141288_-\|general-secretion-pathway-protein-GspD	gnl\|CDD\|274175	TIGR02517, Putative_type_II_secretion_system_protein_D, type II secretion system protein D. In Gram-negative bacteria, proteins that have first crossed the inner member by Sec-dependent protein transport can be exported across the outer membrane by type II secretion, also called the main terminal branch of the general secretion pathway. Members of this family are general secretion pathway protein D. In Yersinia enterocolitica, a second member of this family is part of a novel second type II secretion system specifically associated with virulence (See ). This family is closely homologous to the type IV pilus outer membrane secretin PilQ (TIGR02515) and to the type III secretion system pore YscC/HrcC (TIGR02516). [Protein fate, Protein and peptide secretion and trafficking].	9.50041e-59
NZ_CP036292.1\|WP_145117203.1\|145815_146643_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|370767	pfam09976, TPR_21, Tetratricopeptide repeat-like domain. This family resembles a single unit of a TPR repeat.	1.029e-05
NZ_CP036292.1\|WP_145117201.1\|141608_143516_-\|asparagine-synthase-(glutamine-hydrolyzing)	gnl\|CDD\|223444	COG0367, AsnB, Asparagine synthase (glutamine-hydrolyzing) [Amino acid transport and metabolism].	9.96738e-101
NZ_CP036292.1\|WP_145117199.1\|135959_136613_-\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|238141	cd00229, SGNH_hydrolase, SGNH_hydrolase, or GDSL_hydrolase, is a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the typical Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxlic acid.	8.30981e-18
NZ_CP036292.1\|WP_145117204.1\|146778_147147_-\|DUF2237-family-protein	gnl\|CDD\|378344	pfam09996, DUF2237, Uncharacterized protein conserved in bacteria (DUF2237). This domain, found in various hypothetical bacterial proteins, has no known function.	1.60255e-76
NZ_CP036292.1\|WP_145117206.1\|149941_151366_-\|IS4-family-transposase	gnl\|CDD\|373239	pfam14706, Tnp_DNA_bind, Transposase DNA-binding. This domain occurs at the C-terminus of transposases including E. coli tnpA. TnpA encodes a transposase and an inhibitor protein, the inhibitor only differs from the transposase by the absence of the N-terminal 55 amino acids, which includes most of this domain. This domain consists of alpha helices and turns, and functions as a DNA-binding domain.	2.11318e-18

>NZ_CP036292.1|WP_145117202.1|143902_144994_-|RluA-family-pseudouridine-synthase
MNDHSTDEEPVDEELLDEATSDDQESAAETTYRSIHVPESAQGERIDMYLTQVLDGVSRNQMRMLVHEGGAQVDGRTVRPSFRLRPNQQIRFRMPEPPEDGTIPEPMSLDIVFEDDGMVVVNKPPGMVVHPARGHWSGTLTSGLAYHFQSLSDIGGPTRPGIVHRLDRDTSGVIVVAKTNAVHMNLAAQFADRTVKKQYVAVACGVLSRDRDQIDRPIGRHPYQREKMAIRANHATSKEATTFYEVIERFRGFTYVRLFPKTGRTHQLRVHLDHLRHPILCDKLYGGRSRITADDLAGNYHPQPSAQRETIEPLLTRQALHAQRLELDHPQSGKRMVFEAPVPDDIEAVLKCLRSLNPSENRA
>NZ_CP036292.1|WP_145117201.1|141608_143516_-|asparagine-synthase-(glutamine-hydrolyzing)
MCGILGILDRSGAAPTLTDPQVIAIRDRMAARGPDDATLLRRDNLILAHRRLAIRDPDAGRQPWVSEDGSCALVYNGEIYNDDVLRHTLRSHGFRFRTQCDTEVLMAAWLHWGEKCVEHLRGMFAFGVYDFQKRQLFIARDRFGVKPLFYAELGQQFVFASSIAAITAHPNFRPQPNLSTIRHYLSTFRITLDTETVFAGIQAVRPAETLTLADDKLTSSIYWTPPPRETTGLAFDDAVDRFEETISEAVSIRLRSDVPVGMMLSGGVDSNLLAALLHRNEGVSMTARCGGGIDPELDSAGNDFEYARRCAQHVGFDFDQVTVSATDYHRTWMELIAAYETPISTPTDAIIYRVAQQLKQQVGVALGGEGADEACCGYLIPHWSGNDFDLSRALDSLAPAAAQTARDSLMQQYGTATFASAGDHYLAANGLISAATQASLFHDATWPAAFADGSVERFYDRQFRQLGDLSGVEKTAHLLLRVNLECLLSRLDSATMTAGLESRVPYTDHHFVEQMFRQPFGYCIDVAPGETLQHRTASALAADGSLRGKRLLRAVAGNRMPAELAQRPKASFPTPVPHWLGGQWQPWLQELYRTSPFAQQLFRRDALDELCRLPNHLASWHWPIANTILWGDRWF
>NZ_CP036292.1|WP_145123939.1|137622_141288_-|general-secretion-pathway-protein-GspD
MLAQANQVGEVVIDRTNNRLIVRGGPDAQRVAAESIAALDVVQVTTASDKPVLRALPVPADRLHEIERNVGLQYRKNVDVRITGDEKTGQLLVMAPAGLHDEIQRNVHQAVKGSPEIQQVSANVGQPVRAQFALHNASWRDFEDGLARLAGRKLPVTTQRNGELASFDITSAHAGTTKVQIDRRDNKVTVVAPKTSINGWQRVIETIDRQEHHPGVATQLMRIENAEQAPIRRAVRLLSDIRPVVAQEDDTIGVAGGGRDNPLLRAVMQRQAAAGNGQAGGDDGQAGDAGGDDAFNGLFGDVQIEFVPELGVIIVRGAKRDVQRVMEVIKQIEEQSAVTQPKVEVVALEHANSNAVAEIVNQLYEQVLAPRQGQVSITALDKPNAILLIGRDEAVAGVIDLIKKVDQPVDVASQFRVFNLKHASALDVQATVQGFFVDRPSGNEDLRPGLGARARIIADYRSNSIIAQASPRDMLEVERMIEQLDAPATGAESELKVFKLKNAFAEDLQPVLQAAISGQPEDVPDNTTIPSSTLSILSVDAQGNKTLDSGILSGVVVTADANVNAIIVRAPAASMPLIGELITQLDQLPGAESVVKVFTIVNGDATQLTTSLQELFSAEGQTNSSGVGNLAAMTQTSNSETSLIALRFAVDIRTNSIIASGSATDLEVVESLLIRLDTEGFSARITETIWLRNAAAADVATALQDFVNQQSQLQSRNQFFSQNLGPYDLPERDLIVVPEARTNSLVISVSPRLYEDVRRVIDQLDRRPPMIMIQVVLAEVTLTDGFEFGTELGLQDSVLFDRGVASATSSTPGFNFLPNSSPGLPNANTYDQENLAGQVASAFALGRQSSEFGYGGFVLSAASESVNLLLRMLQDSGRAQILSRPQIMTLDGTEGYVQVGSLFPRIESVQAGNANSGTVIATQDINLGLILRVTPRVGQDGLIVMNVDAQRSNVDPNPNNGQPIATDSNDNPIISPQILITQAQSTVTAMSGQTVVFGGLITKSRRQFSRRVPYVSDIPILGQLFRFDQEIEERTEMLIVLTPRVVNGEEDIQLINDAESSRMSYCLADVVELHGDAGLRGGYGLWGPAVGAMIYPDMHPTVDHFPTAPQDPLLGPGEQIVPGSLQQRPIDPSQQPVQTVPYESSGEVPAIPQAPGLIEQATPIQAADSALNMQPQQRVPMEVFSMQNEATPNNYAMPPGYATPVQYNAPMAAPAAGTPQR
>NZ_CP036292.1|WP_145117200.1|136709_137480_-|hypothetical-protein
MKKFLFILIFAACPIATGCATAPKSESWSAKLPWNKDKPPKPYPNPVKMAVTWTPDILVQPGRTPTRGFGGRVYFYNDHSQAVPVEGELTIHGFDEALASAQHSDGIKRFRFTKEQFTSHFSESDLGASYSIWIPWDAAGGDQKKLSLMSTFKTTGGKVVQSEAAMVVLPGRKVDMTATKRPAVPAVRQVGHYLGTTETHQGLNANSAMQTTTIPLPSSFQQRLARMPEQTKPSKRMTTRLPAAQETSKPTPLPAP
>NZ_CP036292.1|WP_145117199.1|135959_136613_-|SGNH/GDSL-hydrolase-family-protein
MHRICCIALLSLVCSPSVFGQQGVLKPIEDRADLPRVLLIGDSISMGYTVPTRKLLADKANVHRIPANGGPTTRGLANIDKWLGDGDWDLIHFNWGIHDLKHQADGTRQVEPAAYEKNLRALVAKLKATGAKLVWASTTPIPKGKLNPDRTFGDETHYNEIAARVMTELDVPINDLHGYIMPRFDELHRPQDLHYTSAGSDFLAERVADVIEQHLSE
>NZ_CP036292.1|WP_145117198.1|134381_135926_+|diguanylate-cyclase
MGTELVALIALSCGCSGLLCGWFLRNPSGLPQSAAPSSDAEKNRNERDRLEKIAASLRSVTTSVAAEVDAHQTKIQAVSDSLSDSDEDHVLDAVASLIAANAMMQQQLGDAQNQIRSQAAAIESAEEMALTDALTGLNNRRALDRQMTQRHELGDTVAHPTTFMLIDVDHFKNFNDLHGHLTGDEVLKHVGRLLTTSLSDVGFVARYGGEEFAVLFNDMKVAEIKDRADAVRETFGEQEFFVDDQCLQVTASAGLAQLEPGETIESWIERADNALYNAKDEGRNQAYWMDGDVAFPVKSEDEEEAADTLAAAASDQPEESIVEPPEEPIVEPAAESIVGPAEESIVGPSEDPSEESIVEPAAEPTAGPAEETAGGVDVADLTKLSEKVASGFIKLQAERIPFCMLSIRVESDKSDDAWKQITLDCLHTSVRGIDADRIGFDGDRTFIVCLPSTDESVAGERAKTIRQSIDGASGSAWSVEVTTTRATGTETFEEAIQRAIGSSQTADRDEPAIV
>NZ_CP036292.1|WP_145117197.1|132765_134010_-|FAD-dependent-oxidoreductase
MKANYDVVVIGGGPAGSSAAALTAAAGHSTLLIEREAMPRFHIGESLMPEVYWPLQRLGVVDRMEELGFQKKLSVQFVTNSGKESSPFYFKQHDPRECSSTWQVERARFDQMLFERAAELGADCYDQTRLLDVEIDDQDRATGIRVRDAQGQEHTISSRVVVDATGLQSFIANKLGLKEINPDLKKAAIWGYWKNARRDEGENEGATIIMQTEKKDSWFWFIPLSNGITSIGCVGNNDYMLKQGLKPDAKYEHELSICPGLQERLKDAEFQGEIRVAKEFSYTTKRHAGEGWVLIGDAFGFIDPIYSSGVYFALETGVRAADAITEGFAKDDLSGAQLARWADDFKDGSSWIRKLVHAYYTNEFSFGRFMKAHPQHTGNLTDLLIGRIFHDQAGAIFDDMDEAIEAAKRDAMSM
>NZ_CP036292.1|WP_145117196.1|131051_132455_-|hypothetical-protein
MDCKLTRRELLAGLSLTVCAAGPLSAASTDTVPLIPNNEHSLYRVRITVGIEGNAKVPKSELSTDATRKLPVKADSVIDYEERLHRDGDGIAQAAQRYYYEATTKGKVQTNEVESELRRESRHAVLHVAQTRSIVYAAQTQLTTDELELLKVPVNSLAIDRLLPNKSMKVNEAWELESDLLATLFDMDAVQKSAVSATLASFDDATAKVQLLGTISASVDGVPTSLQLRGKLTFDRKQRTVTWLALAIREERGLSKAKPGFEVAAQIRVIRQAITKSNGIDSGEPIDLAIKPTQDKLLVDIRSKQGGFSVFCDRNWHLISENERFAQLRMIDTDRVIAQCDIRPMPKLKDGHQLTLEAFQDDIRRTLDKRFSELLEAEEKVTSGGLRLLRVVAQGAVEEVPVQWIYLHFSDDQGHRSAAIFTLADQQVEAFGGGDHQFAEGFRFTPADDAETKRVASASSLNAPANK
>NZ_CP036292.1|WP_145117195.1|129992_131033_+|deoxyribonuclease
MATRRKKISSLPIGRFIGPPLTIVLFLVVGYLAMTGRLPFLNGASDQAATTEAGLLPGTEGGLQLTSSGDPAAKPIETLTVATFNIQVFGVKKAEDLEVMRYLALILRQFDVIAVQEIRSLERAPVDQLLELINSTGEQYKVILSERLGRTDSKEQYAYFWDSRRIQFVEGSSYLVNDSADFMHREPFVASFHALQAGVPGAKPFSFTMINVHTDPDETDQELNVLDDVFQSVRAYEFSEDDFILAGDLNVEIDKLGELGQIQSVESVNREQTNTAGSRSIDHLLIDRTATTEFRGAGVINYERDLKLPRELADRISDHRPVWAVFDSSEHAPQGVIAALPETVSR
>NZ_CP036292.1|WP_145117194.1|129410_129938_+|hypothetical-protein
MGTQAMTDQPRQDPSNLEHSDPAIRRQTLQSIIDESPRLADWTIPLLRAACDPHASVSELAIATLEDMGAPDASQVADIVAFAQRPADSETVYWATTLIGRIGPAAADAVPTLAGVLANSSFLHVREKAAWALGQIGPAAVGASAVLQSAAEQGPPRLQRLATKALAAMAGSAAA
>NZ_CP036292.1|WP_145117203.1|145815_146643_-|tetratricopeptide-repeat-protein
MKSEERHQLQQNELADALGSGIQSITPYLRAIVIGVIGLIVIVFAYNFVSMRKQAHDATASLDFLLATSNEDPESFKRVSQDFADTMPGQWAQIAQADHNLGAGIESMFVDRDEATGFLEAATENYKSVLATAKDPLLKTRANLGLAKAYEAQGDLDQAIATYEIVADNTSSEALAEQAKERIRLLGTDDVRDFYTWFRENQPVSMASIAPGLPGLEDLPDGPAEGLPPAETPDLKDVEVSDAPEAEAKEEAAAAPKEEAAEAKDAAAEEPAKTE
>NZ_CP036292.1|WP_145117204.1|146778_147147_-|DUF2237-family-protein
MSKAKNVLGTPLQTCSVDPMTGFYRTGCCDTGREDVGLHIVCTQVTAEFLEFSKSVGNDLSTPVAEYGFPGLKPGNRWCLCALRWKEAWQAGMAPPVVLDATHISTLEFIDLEVLQAHAADG
>NZ_CP036292.1|WP_145117205.1|147466_149782_+|AAA-family-ATPase
MDLILDNLTDPQRAAVTHMDGPMLMLAGPGSGKTRVVTHRIAHLLREGVPASQILALTFTNKAAEEMLARVQQLAPGEPVWMSTFHRFCARMLRQYSSLVGLQENYSIYDMADAKATMKRAIEVSGISLSHTSPDQIANAISHFKNQLLTPESMEGANLPAGKMLAAKVYPYYQQLLLVANAVDFDCMLLHVARMLRENPELREALDSRFRYIMVDEYQDTNLAQYAIVRSLSVVHQNLAVTGDPDQSIYGWRGANLNNILDFENDYPQVKTVRLEQNYRSTPNILRVADQLITNNTRRKHKGLYTHNPEGAAVRLRIYANGYQEADDIADQIVEQIQNHGRSPKDFAILCRMNYLTRSLEHSLRSRVVPYTIVRGVEFYQRKEIKDLLSYLQLINNPANDAALSRIVNTPARGIGKTTMDRVMLFAARHRIPLFEAICRCDEIESIKPRTRGLLKRFVGIIDALSRKASSSLEDLLRFVLEQTQYSDYLRFSTVEGEDNDALANVDELVSAAVEFDRQHPDDGSLETFLEQVALISDTDAWEESSDRVTLMTLHAAKGLEFPCVYIIGVEDQVLPHHRSHDDPMQFEEERRLLFVGITRAEQTLQLSMAKLRSARGSMRPAAASPFLLELPREEMQVIDAHQPTQYGDDNDFDVDVEYPEAWDMHADHDDDLNQLPPEERTPETTSTPRTAPIASVTTAAQMLEQQMANTIDPEIYTVGMIVSHPEYGSGRIQSLSGSGGKRTATVNFFVDSIERRFRLSHAQLTPESED
>NZ_CP036292.1|WP_145117206.1|149941_151366_-|IS4-family-transposase
MQPTSIAYEFQDIQLGDKRLNDRAEALLASLAANPSASINEACSGWDETKAAYRLFDNPNVDPEAILGAHAEKTLQRIKAQDTVCIAQDTTELDYTAHPPEGVRNLDRLGRRGLYDHSHIAFTPEKLCLGVVGVKFYDRDKESLGTSKKREGQPLHTGEGQRWLDGYRKACEIAGKCPETQIVSLADREGDIYDIFVEADQHETPAQFVIRSQRKRSLPEKDPDGGPAAYKKMRAEIASAQPVAYREVQLPQTPKRTKGSGNKQHPGREARTAKLEIRAKRMTLRAPHNKQSSMPPVEISVVWVREIDGPGDGTEVDWLLLSSLPVDTIAQTLRIVDLYVARWPIEVFFRVFKTGCRVEEIQLEARDRLIRALMFYKVIAWRIMFVTFLGRECPELPCDVVFSEAEWKSVWKVVEKTAPPKQAPELSQFIPVLATLGGYNHRQGDGPPGAEVIWRGTRRMLDFALCWQAFGPDQ
>NZ_CP036292.1|WP_145117207.1|151759_152827_+|hypothetical-protein
MKVLVCPQLLLMSMLMAAPVFAQVVPGTGTKIDYVGDDFEEPGWEFVHNMPKGSHENNERRNGPSGYSKNRRFIEGPERGQPDHMQIIPTPAGGLPHSKNALWVSTLHSGIPGQNTRTVEQDDLIVSCPSRLGTSFRPSESPNCMVRIYFPEADRWEKRNGPHFGFRLGCSTTAEQEREGFLAFGTEMGPEPYWPGIWVHYRHTADQRGPAGSAYLAVRGDNRGRDFRVAEMEQFGWWTFGISVTPDGRIHYYASPGVDPLTPQDLLTSQTPYGFNAERVSSFFFNFCNVNDGRTWSTPVVIDDPEMYLVNASRVMQFVQRKEAAEAKRQAYAKRRAEMMAERNARSQNNSRSSR
>NZ_CP036292.1|WP_145117208.1|153403_159529_-|hypothetical-protein
MIAARSASLFLLYTIGFTAATVFSQEESPTPEQAAAIATAAEGLGSPRFDVRERSMRELWQIGLPSREKLEQLVAEGGSEAQMRARRVLRDFQYGVLPTTPPRLRQLIGKFRDGRGKQRFEAMEGLRGERALAVIENLISLEPNAPLRTAYLIQLVSDPAIIDDYAGPQQMVDLVQRVGGDQDAGWQRDTTAALVFSPLLVSTLAKDDQLDQLDQFVAALKPEDRSRYLAAFYTNPTSLQILVQASRHGFLLKMLQHETDPSSRNTLALRLFSQQQVTQGLAQRGGLIDSLGELPNHVDNATMQTLLQVVLRQSATISAILTRSGFDGLLKLSQQIEDPDDRVSALAMIVANRTVIAQLKSEDKLGKIVDLATDQPDDARRLAYLKAIVKANILNTLAAADAMPMVKDLWRRIEASEDRALQHDAILRMVRIPNLMELIKDRAAAESLLEMIGTMDKNLLPNVLPVLVHNVDLMRFLSNADLIDKLVAIHCDVPEPHRTRVLGQLVSKMATWQRDPAKRMTLLWKTVDRLPAEARPSYLEALGRLRLEPAMARQLVSRLLHETPDDQRDASIEAVLQSRALSSVVREPHDLQALVDRLPMVDEKTLATFATLILTDQPFRQAILDAGHLATLTAQFCRLDPKQSAALMSRMLQSREAQSEIAKPEGVAQLIAIGKQQEPNHKLQVFEAIAANQAAMQQVLDSDQLDPLLELLNAPPTQQQISAVSRLMNNSHVLTHLIQHDQLGRLLAIPQEDWPTEALDRFAQRLFSSLVISMHEKQNKLERIPELVHSDLPPAIATAFANQILSDYRLMRAAIKQGRLIDTFEVALRGEGLSEPASRTLVANTNSVKAFAEAMRLPDLIAAITKERRNLPIDRRAQSLFSSTALLNNLLETNQIDLLYGVVKSQTNPTDKSAILKRMMVQRYSISRLIQKDQFEPLWDLIQTEASAEMQPLLESYLLVTAYDRSVADSTPPWDGKLQTLHGQIDQLADTPIRREAIGLLATARLSGYPEEHTAHAKQIARWIDQQTDASVATLWSNRLIVAIDPSAIIQAGRTDLLADIIADKALPQRTVAALTKKPETVEALQQAKLLKRLVEACDRSPQQDALRTVLLQSPAMTERLDRATQIRPWLKEFFSMKGDSQRDAALRNVLKQQHLLALAIEENYFDTLTDWVKATGQSPSMRSRGGVPAAMFGFLVQPVCVATLERQKRGAELLETLAEVETPYLQYRLLNDMAHIDEAVECIARHGGLQMLLPILEKLSSSQRHMLLSRLVFGPGRLSVWIDNTPPATVEKLFGSLSDQLKRSCLRLASLRPEELLRSKRVVELVFEIWESAPQADRHMFLQRLVPDPKARWHLLQRGQYEPLLQLIDQLPNPASYRHELIYSDAGAVAHKIAHGEFDEAERLLQENTDSEIGKSNLAAFWLQRGVLSEQIAEHKDSPLLPFLLRANGQPEEAAQWAREQNNLPLATWIDAGAGRWDRAADQQKQILDELIETENDDDMLRLSVLCGLASYQRQAKRDADTDETLDRAERLADKIATPAAQIALMNCLLVNDRIDRALEIAKTHAPQTHFELLRARGDYDAALQAVAWKSDDPAAWVAERLNVDMQQTIPLDAVQIVAKVGWILDQREAAEQAHTLYAALSEQIHSQQKDPRRSNLLHQKELFRILRDSGRMPLAVAPLLDELKLIGRPTGMNIIGHMGQRITPSRRVLERMGYLNTPRILQPAIGDLVTEFDGWWSHFAGKSPGDSDDQLMQRVKNVDAMLAGEGTVEIDGQTTSPEEYLAAELKELEKTPLTAEQLSAFVGAMLRFDQTQQAFDLMQQQRETELPAAQAGIIYRRLGKWAEAAEAFQQAWENDVLQLEFRYLAADALARSGDREAGAKQMQTASMMAVNFRIRNALTHRLRELGAQPLAAKEARLLQAVSPIGSFTWYKSCQRRADLETDPATVADLQQTTMLQFAGGWTKEIPLSDLASLHRIHRMRAAAAIEADDFEKAQQHIDRMLNLNRIDPQNGEQLIPALRAAGRDKQADALQGKLIVTSR
>NZ_CP036292.1|WP_145117209.1|159731_160373_-|DUF1080-domain-containing-protein
MRRLFACFLLLFPIVAVAQSPAPESGFTPLFDGKSLQGWEGDANWFRVDDGAIVAGSASETIPNNFFLATTEQYEDFELRLEAKLVGAGQNAGVQFRTRRIPNHHEVSGYQADMGTAGGKPIWGSLYDESRRNKMLAVPDPAAVEAVLKTDDWNRIRVRCQGARIQIWLNDLQTVDYTETDPQIERTGIIALQIHGGKPALASYRNIRIQRLK
>NZ_CP036292.1|WP_145117210.1|160620_162300_+|dihydroxy-acid-dehydratase
MNAPLNKYSSRVTQPKSQGASQAMLYGTGMTSEDMNKAQVGIGSVWYEGNTCNMHLLDLANEVKEGVRAADMVGMRFNTVGVSDGISMGTEGMSFSLQSRDLIADSIETIMGGQWYDGLVALPGCDKNMPGCLIAMGRLNRPSIMVYGGTIRAGKWNGQKLDIVNAFQCYGQYLSGDIDESERQNIVKCSIPGAGACGGMYTANTMATAIEALGMTLPYSASIPAEDPAKKDECRRAGAAIRVLLERDIKPRDIMTRQAFENAMAVIMAVGGSTNAVLHLIAMARAVDINLTIDDFQAVSDRVPYIADLKPSGKFVQEDLHSVGGTPALMKYLLAEGVITGDCMTVTGKTLGENLADVPDLDPGQEIIRPLDKPIKASGHIRILRGNLAPEGAVAKITGKEGLLFTGTARCFDSEEEMLTALEEKKIVKGDVVIIRYEGPKGGPGMPEMLTPTSAIMGAGLGADVALMTDGRFSGGSHGFIVGHVTPEAQEGGPIALARDGDKITIDAEKLEINIDVSDEELAKRREEFVAPPLKATRGTLYKYIKNVKSASEGCVTDE
>NZ_CP036292.1|WP_145123940.1|162642_163395_+|TIM-barrel-protein
MGWCFKPIPSIELAKHCKAIGIEAIEGIPASDYPAVTELGLKISLVGSHGFQNGPLDPENHAMNEAKLREAIDTAVKFGAPSVITFTGMRKTGIDDRQATKNCLDLWKRVLPYAEANDITLVLEHLNSRDDTHPMKGHPGYWGDDVELCVDLVKQLDSPRFKLLFDIYHVQIMNGDIIRRIREYHPLIGHYHTAGSPGRGELNDDQEINYPAVMRAILETGYSQYVAQEFIPTSNDPIASLREAARVCDV
>NZ_CP036292.1|WP_145117211.1|163564_166189_+|hypothetical-protein
MATRTIERIDETHSVGPRVRVDDFVRLGIGVREARVGVIRRAAGDATAAVALDEPTDTRHGFDDRIASIAASTYRLLDPRGRNELMQRVQLLQLESPPAQVKPWWKPRHATVVTQDELRDRFDPSAADDTYLPVGLQAEAGWKTVARRMGLFPFSRRAVWVASAMASVSILIVLPIVIAMSSADDPPSGELTAAATTVSAAPEPIARQLGSAAASPQLTTDFPVAEVDEPAPAAEPVSPFAEAFVVPSESDGLEASPSESEPMPVHRSLPGTAPSSADPLVFVPNVEPSATLEDAPSVAPESPSTPAPITDPESTEPKSLESESIEPMPADAASSDSPMPTADVPTDPMPPVPATPAPIATPVAPPAAAADPAVDPFAQVDLQPAVEADGGLQDSRFPKPSADEIAVATERLARLRADLPAANTDADLVSNIRKLLQTATESEPGSADRWVLLLESSQHLLMMGRGADAQQALLQLTREYQASEVQLRQLLLEPLINGAQTITQKERVIGWALSTSELLLRAEEFDSAATTLRGATTLAVKLGDNDLRVRINLQSDAIKQAKRIAPLATKALAESTPTTASASAANSVGRYLCLYLYDWPQGLPWLKHASTPKLAKVAQMEIDTAAAPDSTLDLVNSWIECAADVRGRGGESILLHARDLVAEAMLESSGLKAKDLERKLAELDAMLPADLRTVAPTPSIAAAPAAAMPAGNLTGMLGRLKADGLDVSALIRYDAGLNLTHDAFSQILDQLGIQAGTISLEFVGLIDLPENSTIRFVTSTGTDKADAVVVAVNNQTVPLSVEGQRNRKAGTVDLPAGSHLVRWQFGGKQLATCHLVVEDDRAKKPLTLRHTPALLEQVLSVAPARLRVNVVRAN

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Crispr_ID: NZ_CP036292_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_2

152887-152996

Orphan

Consensus_repeat	Method
CATGCAATAGCCTGGGACGCAAGTCCCAGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_2

>merge|NZ_CP036292|2|152887-152996|CRISPRCasFinder
CATGCAATAGCCTGGGACGCAAGTCCCAGGACCCCAGGACCAAGCGACCAAACCATGCCGCCCGAGTCGCGAAGCGACGTCATGCAAAAGCCTGGGACGCAAGTCCCAGG

>NZ_CP036292|2|2|152887-152996|CRISPRCasFinder
CATGCAATAGCCTGGGACGCAAGTCCCAGG	ACCCCAGGACCAAGCGACCAAACCATGCCGCCCGAGTCGCGAAGCGACGT
CATGCAAAAGCCTGGGACGCAAGTCCCAGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123940.1\|162642_163395_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|226149
NZ_CP036292.1\|WP_145117210.1\|160620_162300_+\|dihydroxy-acid-dehydratase	unknown	unknown	gnl\|CDD\|234861
NZ_CP036292.1\|WP_145117209.1\|159731_160373_-\|DUF1080-domain-containing-protein	unknown	unknown	gnl\|CDD\|368908
NZ_CP036292.1\|WP_145117211.1\|163564_166189_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235906
NZ_CP036292.1\|WP_145117216.1\|171830_175106_-\|efflux-RND-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223911
NZ_CP036292.1\|WP_145117213.1\|167119_167425_-\|transposase	unknown	unknown	gnl\|CDD\|225511
NZ_CP036292.1\|WP_145117208.1\|153403_159529_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117214.1\|168001_169426_+\|magnesium-chelatase	unknown	unknown	gnl\|CDD\|224160
NZ_CP036292.1\|WP_145117205.1\|147466_149782_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|273429
NZ_CP036292.1\|WP_145117215.1\|169628_171329_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227204
NZ_CP036292.1\|WP_145117202.1\|143902_144994_-\|RluA-family-pseudouridine-synthase	unknown	unknown	gnl\|CDD\|223638
NZ_CP036292.1\|WP_145123939.1\|137622_141288_-\|general-secretion-pathway-protein-GspD	unknown	unknown	gnl\|CDD\|274175
NZ_CP036292.1\|WP_145117212.1\|166238_167123_-\|IS3-family-transposase	unknown	unknown	gnl\|CDD\|222853
NZ_CP036292.1\|WP_145117200.1\|136709_137480_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117203.1\|145815_146643_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|370767
NZ_CP036292.1\|WP_145117201.1\|141608_143516_-\|asparagine-synthase-(glutamine-hydrolyzing)	unknown	unknown	gnl\|CDD\|223444
NZ_CP036292.1\|WP_145117207.1\|151759_152827_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117199.1\|135959_136613_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|238141
NZ_CP036292.1\|WP_145117204.1\|146778_147147_-\|DUF2237-family-protein	unknown	unknown	gnl\|CDD\|378344
NZ_CP036292.1\|WP_145117206.1\|149941_151366_-\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|373239

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123940.1\|162642_163395_+\|TIM-barrel-protein	gnl\|CDD\|226149	COG3622, Hfi, Hydroxypyruvate isomerase [Carbohydrate transport and metabolism].	5.27215e-31
NZ_CP036292.1\|WP_145117209.1\|159731_160373_-\|DUF1080-domain-containing-protein	gnl\|CDD\|368908	pfam06439, DUF1080, Domain of Unknown Function (DUF1080). This family has structural similarity to an endo-1,3-1,4-beta glucanase belonging to glycoside hydrolase family 16. However, the structure surrounding the active site differs from that of the endo-1,3-1,4-beta glucanase.	3.57705e-49
NZ_CP036292.1\|WP_145117211.1\|163564_166189_+\|hypothetical-protein	gnl\|CDD\|235906	PRK07003, PRK07003, DNA polymerase III subunit gamma/tau.	3.80964e-08
NZ_CP036292.1\|WP_145117216.1\|171830_175106_-\|efflux-RND-transporter-permease-subunit	gnl\|CDD\|223911	COG0841, AcrB, Cation/multidrug efflux pump [Defense mechanisms].	0
NZ_CP036292.1\|WP_145117213.1\|167119_167425_-\|transposase	gnl\|CDD\|225511	COG2963, COG2963, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	8.08038e-08
NZ_CP036292.1\|WP_145117214.1\|168001_169426_+\|magnesium-chelatase	gnl\|CDD\|224160	COG1239, ChlI, Mg-chelatase subunit ChlI [Coenzyme metabolism].	1.20087e-48
NZ_CP036292.1\|WP_145117205.1\|147466_149782_+\|AAA-family-ATPase	gnl\|CDD\|273429	TIGR01073, ATP-dependent_DNA_helicase_PcrA, ATP-dependent DNA helicase PcrA. Designed to identify pcrA members of the uvrD/rep subfamily. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP036292.1\|WP_145117215.1\|169628_171329_+\|hypothetical-protein	gnl\|CDD\|227204	COG4867, COG4867, Uncharacterized protein with a von Willebrand factor type A (vWA) domain [General function prediction only].	3.02832e-42
NZ_CP036292.1\|WP_145117210.1\|160620_162300_+\|dihydroxy-acid-dehydratase	gnl\|CDD\|234861	PRK00911, PRK00911, dihydroxy-acid dehydratase; Provisional.	0
NZ_CP036292.1\|WP_145123939.1\|137622_141288_-\|general-secretion-pathway-protein-GspD	gnl\|CDD\|274175	TIGR02517, Putative_type_II_secretion_system_protein_D, type II secretion system protein D. In Gram-negative bacteria, proteins that have first crossed the inner member by Sec-dependent protein transport can be exported across the outer membrane by type II secretion, also called the main terminal branch of the general secretion pathway. Members of this family are general secretion pathway protein D. In Yersinia enterocolitica, a second member of this family is part of a novel second type II secretion system specifically associated with virulence (See ). This family is closely homologous to the type IV pilus outer membrane secretin PilQ (TIGR02515) and to the type III secretion system pore YscC/HrcC (TIGR02516). [Protein fate, Protein and peptide secretion and trafficking].	9.50041e-59
NZ_CP036292.1\|WP_145117212.1\|166238_167123_-\|IS3-family-transposase	gnl\|CDD\|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	7.3877e-74
NZ_CP036292.1\|WP_145117203.1\|145815_146643_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|370767	pfam09976, TPR_21, Tetratricopeptide repeat-like domain. This family resembles a single unit of a TPR repeat.	1.029e-05
NZ_CP036292.1\|WP_145117201.1\|141608_143516_-\|asparagine-synthase-(glutamine-hydrolyzing)	gnl\|CDD\|223444	COG0367, AsnB, Asparagine synthase (glutamine-hydrolyzing) [Amino acid transport and metabolism].	9.96738e-101
NZ_CP036292.1\|WP_145117199.1\|135959_136613_-\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|238141	cd00229, SGNH_hydrolase, SGNH_hydrolase, or GDSL_hydrolase, is a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the typical Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxlic acid.	8.30981e-18
NZ_CP036292.1\|WP_145117204.1\|146778_147147_-\|DUF2237-family-protein	gnl\|CDD\|378344	pfam09996, DUF2237, Uncharacterized protein conserved in bacteria (DUF2237). This domain, found in various hypothetical bacterial proteins, has no known function.	1.60255e-76
NZ_CP036292.1\|WP_145117206.1\|149941_151366_-\|IS4-family-transposase	gnl\|CDD\|373239	pfam14706, Tnp_DNA_bind, Transposase DNA-binding. This domain occurs at the C-terminus of transposases including E. coli tnpA. TnpA encodes a transposase and an inhibitor protein, the inhibitor only differs from the transposase by the absence of the N-terminal 55 amino acids, which includes most of this domain. This domain consists of alpha helices and turns, and functions as a DNA-binding domain.	2.11318e-18
NZ_CP036292.1\|WP_145117202.1\|143902_144994_-\|RluA-family-pseudouridine-synthase	gnl\|CDD\|223638	COG0564, RluA, Pseudouridylate synthases, 23S RNA-specific [Translation, ribosomal structure and biogenesis].	4.02839e-101

>NZ_CP036292.1|WP_145117207.1|151759_152827_+|hypothetical-protein
MKVLVCPQLLLMSMLMAAPVFAQVVPGTGTKIDYVGDDFEEPGWEFVHNMPKGSHENNERRNGPSGYSKNRRFIEGPERGQPDHMQIIPTPAGGLPHSKNALWVSTLHSGIPGQNTRTVEQDDLIVSCPSRLGTSFRPSESPNCMVRIYFPEADRWEKRNGPHFGFRLGCSTTAEQEREGFLAFGTEMGPEPYWPGIWVHYRHTADQRGPAGSAYLAVRGDNRGRDFRVAEMEQFGWWTFGISVTPDGRIHYYASPGVDPLTPQDLLTSQTPYGFNAERVSSFFFNFCNVNDGRTWSTPVVIDDPEMYLVNASRVMQFVQRKEAAEAKRQAYAKRRAEMMAERNARSQNNSRSSR
>NZ_CP036292.1|WP_145117206.1|149941_151366_-|IS4-family-transposase
MQPTSIAYEFQDIQLGDKRLNDRAEALLASLAANPSASINEACSGWDETKAAYRLFDNPNVDPEAILGAHAEKTLQRIKAQDTVCIAQDTTELDYTAHPPEGVRNLDRLGRRGLYDHSHIAFTPEKLCLGVVGVKFYDRDKESLGTSKKREGQPLHTGEGQRWLDGYRKACEIAGKCPETQIVSLADREGDIYDIFVEADQHETPAQFVIRSQRKRSLPEKDPDGGPAAYKKMRAEIASAQPVAYREVQLPQTPKRTKGSGNKQHPGREARTAKLEIRAKRMTLRAPHNKQSSMPPVEISVVWVREIDGPGDGTEVDWLLLSSLPVDTIAQTLRIVDLYVARWPIEVFFRVFKTGCRVEEIQLEARDRLIRALMFYKVIAWRIMFVTFLGRECPELPCDVVFSEAEWKSVWKVVEKTAPPKQAPELSQFIPVLATLGGYNHRQGDGPPGAEVIWRGTRRMLDFALCWQAFGPDQ
>NZ_CP036292.1|WP_145117205.1|147466_149782_+|AAA-family-ATPase
MDLILDNLTDPQRAAVTHMDGPMLMLAGPGSGKTRVVTHRIAHLLREGVPASQILALTFTNKAAEEMLARVQQLAPGEPVWMSTFHRFCARMLRQYSSLVGLQENYSIYDMADAKATMKRAIEVSGISLSHTSPDQIANAISHFKNQLLTPESMEGANLPAGKMLAAKVYPYYQQLLLVANAVDFDCMLLHVARMLRENPELREALDSRFRYIMVDEYQDTNLAQYAIVRSLSVVHQNLAVTGDPDQSIYGWRGANLNNILDFENDYPQVKTVRLEQNYRSTPNILRVADQLITNNTRRKHKGLYTHNPEGAAVRLRIYANGYQEADDIADQIVEQIQNHGRSPKDFAILCRMNYLTRSLEHSLRSRVVPYTIVRGVEFYQRKEIKDLLSYLQLINNPANDAALSRIVNTPARGIGKTTMDRVMLFAARHRIPLFEAICRCDEIESIKPRTRGLLKRFVGIIDALSRKASSSLEDLLRFVLEQTQYSDYLRFSTVEGEDNDALANVDELVSAAVEFDRQHPDDGSLETFLEQVALISDTDAWEESSDRVTLMTLHAAKGLEFPCVYIIGVEDQVLPHHRSHDDPMQFEEERRLLFVGITRAEQTLQLSMAKLRSARGSMRPAAASPFLLELPREEMQVIDAHQPTQYGDDNDFDVDVEYPEAWDMHADHDDDLNQLPPEERTPETTSTPRTAPIASVTTAAQMLEQQMANTIDPEIYTVGMIVSHPEYGSGRIQSLSGSGGKRTATVNFFVDSIERRFRLSHAQLTPESED
>NZ_CP036292.1|WP_145117204.1|146778_147147_-|DUF2237-family-protein
MSKAKNVLGTPLQTCSVDPMTGFYRTGCCDTGREDVGLHIVCTQVTAEFLEFSKSVGNDLSTPVAEYGFPGLKPGNRWCLCALRWKEAWQAGMAPPVVLDATHISTLEFIDLEVLQAHAADG
>NZ_CP036292.1|WP_145117203.1|145815_146643_-|tetratricopeptide-repeat-protein
MKSEERHQLQQNELADALGSGIQSITPYLRAIVIGVIGLIVIVFAYNFVSMRKQAHDATASLDFLLATSNEDPESFKRVSQDFADTMPGQWAQIAQADHNLGAGIESMFVDRDEATGFLEAATENYKSVLATAKDPLLKTRANLGLAKAYEAQGDLDQAIATYEIVADNTSSEALAEQAKERIRLLGTDDVRDFYTWFRENQPVSMASIAPGLPGLEDLPDGPAEGLPPAETPDLKDVEVSDAPEAEAKEEAAAAPKEEAAEAKDAAAEEPAKTE
>NZ_CP036292.1|WP_145117202.1|143902_144994_-|RluA-family-pseudouridine-synthase
MNDHSTDEEPVDEELLDEATSDDQESAAETTYRSIHVPESAQGERIDMYLTQVLDGVSRNQMRMLVHEGGAQVDGRTVRPSFRLRPNQQIRFRMPEPPEDGTIPEPMSLDIVFEDDGMVVVNKPPGMVVHPARGHWSGTLTSGLAYHFQSLSDIGGPTRPGIVHRLDRDTSGVIVVAKTNAVHMNLAAQFADRTVKKQYVAVACGVLSRDRDQIDRPIGRHPYQREKMAIRANHATSKEATTFYEVIERFRGFTYVRLFPKTGRTHQLRVHLDHLRHPILCDKLYGGRSRITADDLAGNYHPQPSAQRETIEPLLTRQALHAQRLELDHPQSGKRMVFEAPVPDDIEAVLKCLRSLNPSENRA
>NZ_CP036292.1|WP_145117201.1|141608_143516_-|asparagine-synthase-(glutamine-hydrolyzing)
MCGILGILDRSGAAPTLTDPQVIAIRDRMAARGPDDATLLRRDNLILAHRRLAIRDPDAGRQPWVSEDGSCALVYNGEIYNDDVLRHTLRSHGFRFRTQCDTEVLMAAWLHWGEKCVEHLRGMFAFGVYDFQKRQLFIARDRFGVKPLFYAELGQQFVFASSIAAITAHPNFRPQPNLSTIRHYLSTFRITLDTETVFAGIQAVRPAETLTLADDKLTSSIYWTPPPRETTGLAFDDAVDRFEETISEAVSIRLRSDVPVGMMLSGGVDSNLLAALLHRNEGVSMTARCGGGIDPELDSAGNDFEYARRCAQHVGFDFDQVTVSATDYHRTWMELIAAYETPISTPTDAIIYRVAQQLKQQVGVALGGEGADEACCGYLIPHWSGNDFDLSRALDSLAPAAAQTARDSLMQQYGTATFASAGDHYLAANGLISAATQASLFHDATWPAAFADGSVERFYDRQFRQLGDLSGVEKTAHLLLRVNLECLLSRLDSATMTAGLESRVPYTDHHFVEQMFRQPFGYCIDVAPGETLQHRTASALAADGSLRGKRLLRAVAGNRMPAELAQRPKASFPTPVPHWLGGQWQPWLQELYRTSPFAQQLFRRDALDELCRLPNHLASWHWPIANTILWGDRWF
>NZ_CP036292.1|WP_145123939.1|137622_141288_-|general-secretion-pathway-protein-GspD
MLAQANQVGEVVIDRTNNRLIVRGGPDAQRVAAESIAALDVVQVTTASDKPVLRALPVPADRLHEIERNVGLQYRKNVDVRITGDEKTGQLLVMAPAGLHDEIQRNVHQAVKGSPEIQQVSANVGQPVRAQFALHNASWRDFEDGLARLAGRKLPVTTQRNGELASFDITSAHAGTTKVQIDRRDNKVTVVAPKTSINGWQRVIETIDRQEHHPGVATQLMRIENAEQAPIRRAVRLLSDIRPVVAQEDDTIGVAGGGRDNPLLRAVMQRQAAAGNGQAGGDDGQAGDAGGDDAFNGLFGDVQIEFVPELGVIIVRGAKRDVQRVMEVIKQIEEQSAVTQPKVEVVALEHANSNAVAEIVNQLYEQVLAPRQGQVSITALDKPNAILLIGRDEAVAGVIDLIKKVDQPVDVASQFRVFNLKHASALDVQATVQGFFVDRPSGNEDLRPGLGARARIIADYRSNSIIAQASPRDMLEVERMIEQLDAPATGAESELKVFKLKNAFAEDLQPVLQAAISGQPEDVPDNTTIPSSTLSILSVDAQGNKTLDSGILSGVVVTADANVNAIIVRAPAASMPLIGELITQLDQLPGAESVVKVFTIVNGDATQLTTSLQELFSAEGQTNSSGVGNLAAMTQTSNSETSLIALRFAVDIRTNSIIASGSATDLEVVESLLIRLDTEGFSARITETIWLRNAAAADVATALQDFVNQQSQLQSRNQFFSQNLGPYDLPERDLIVVPEARTNSLVISVSPRLYEDVRRVIDQLDRRPPMIMIQVVLAEVTLTDGFEFGTELGLQDSVLFDRGVASATSSTPGFNFLPNSSPGLPNANTYDQENLAGQVASAFALGRQSSEFGYGGFVLSAASESVNLLLRMLQDSGRAQILSRPQIMTLDGTEGYVQVGSLFPRIESVQAGNANSGTVIATQDINLGLILRVTPRVGQDGLIVMNVDAQRSNVDPNPNNGQPIATDSNDNPIISPQILITQAQSTVTAMSGQTVVFGGLITKSRRQFSRRVPYVSDIPILGQLFRFDQEIEERTEMLIVLTPRVVNGEEDIQLINDAESSRMSYCLADVVELHGDAGLRGGYGLWGPAVGAMIYPDMHPTVDHFPTAPQDPLLGPGEQIVPGSLQQRPIDPSQQPVQTVPYESSGEVPAIPQAPGLIEQATPIQAADSALNMQPQQRVPMEVFSMQNEATPNNYAMPPGYATPVQYNAPMAAPAAGTPQR
>NZ_CP036292.1|WP_145117200.1|136709_137480_-|hypothetical-protein
MKKFLFILIFAACPIATGCATAPKSESWSAKLPWNKDKPPKPYPNPVKMAVTWTPDILVQPGRTPTRGFGGRVYFYNDHSQAVPVEGELTIHGFDEALASAQHSDGIKRFRFTKEQFTSHFSESDLGASYSIWIPWDAAGGDQKKLSLMSTFKTTGGKVVQSEAAMVVLPGRKVDMTATKRPAVPAVRQVGHYLGTTETHQGLNANSAMQTTTIPLPSSFQQRLARMPEQTKPSKRMTTRLPAAQETSKPTPLPAP
>NZ_CP036292.1|WP_145117199.1|135959_136613_-|SGNH/GDSL-hydrolase-family-protein
MHRICCIALLSLVCSPSVFGQQGVLKPIEDRADLPRVLLIGDSISMGYTVPTRKLLADKANVHRIPANGGPTTRGLANIDKWLGDGDWDLIHFNWGIHDLKHQADGTRQVEPAAYEKNLRALVAKLKATGAKLVWASTTPIPKGKLNPDRTFGDETHYNEIAARVMTELDVPINDLHGYIMPRFDELHRPQDLHYTSAGSDFLAERVADVIEQHLSE
>NZ_CP036292.1|WP_145117208.1|153403_159529_-|hypothetical-protein
MIAARSASLFLLYTIGFTAATVFSQEESPTPEQAAAIATAAEGLGSPRFDVRERSMRELWQIGLPSREKLEQLVAEGGSEAQMRARRVLRDFQYGVLPTTPPRLRQLIGKFRDGRGKQRFEAMEGLRGERALAVIENLISLEPNAPLRTAYLIQLVSDPAIIDDYAGPQQMVDLVQRVGGDQDAGWQRDTTAALVFSPLLVSTLAKDDQLDQLDQFVAALKPEDRSRYLAAFYTNPTSLQILVQASRHGFLLKMLQHETDPSSRNTLALRLFSQQQVTQGLAQRGGLIDSLGELPNHVDNATMQTLLQVVLRQSATISAILTRSGFDGLLKLSQQIEDPDDRVSALAMIVANRTVIAQLKSEDKLGKIVDLATDQPDDARRLAYLKAIVKANILNTLAAADAMPMVKDLWRRIEASEDRALQHDAILRMVRIPNLMELIKDRAAAESLLEMIGTMDKNLLPNVLPVLVHNVDLMRFLSNADLIDKLVAIHCDVPEPHRTRVLGQLVSKMATWQRDPAKRMTLLWKTVDRLPAEARPSYLEALGRLRLEPAMARQLVSRLLHETPDDQRDASIEAVLQSRALSSVVREPHDLQALVDRLPMVDEKTLATFATLILTDQPFRQAILDAGHLATLTAQFCRLDPKQSAALMSRMLQSREAQSEIAKPEGVAQLIAIGKQQEPNHKLQVFEAIAANQAAMQQVLDSDQLDPLLELLNAPPTQQQISAVSRLMNNSHVLTHLIQHDQLGRLLAIPQEDWPTEALDRFAQRLFSSLVISMHEKQNKLERIPELVHSDLPPAIATAFANQILSDYRLMRAAIKQGRLIDTFEVALRGEGLSEPASRTLVANTNSVKAFAEAMRLPDLIAAITKERRNLPIDRRAQSLFSSTALLNNLLETNQIDLLYGVVKSQTNPTDKSAILKRMMVQRYSISRLIQKDQFEPLWDLIQTEASAEMQPLLESYLLVTAYDRSVADSTPPWDGKLQTLHGQIDQLADTPIRREAIGLLATARLSGYPEEHTAHAKQIARWIDQQTDASVATLWSNRLIVAIDPSAIIQAGRTDLLADIIADKALPQRTVAALTKKPETVEALQQAKLLKRLVEACDRSPQQDALRTVLLQSPAMTERLDRATQIRPWLKEFFSMKGDSQRDAALRNVLKQQHLLALAIEENYFDTLTDWVKATGQSPSMRSRGGVPAAMFGFLVQPVCVATLERQKRGAELLETLAEVETPYLQYRLLNDMAHIDEAVECIARHGGLQMLLPILEKLSSSQRHMLLSRLVFGPGRLSVWIDNTPPATVEKLFGSLSDQLKRSCLRLASLRPEELLRSKRVVELVFEIWESAPQADRHMFLQRLVPDPKARWHLLQRGQYEPLLQLIDQLPNPASYRHELIYSDAGAVAHKIAHGEFDEAERLLQENTDSEIGKSNLAAFWLQRGVLSEQIAEHKDSPLLPFLLRANGQPEEAAQWAREQNNLPLATWIDAGAGRWDRAADQQKQILDELIETENDDDMLRLSVLCGLASYQRQAKRDADTDETLDRAERLADKIATPAAQIALMNCLLVNDRIDRALEIAKTHAPQTHFELLRARGDYDAALQAVAWKSDDPAAWVAERLNVDMQQTIPLDAVQIVAKVGWILDQREAAEQAHTLYAALSEQIHSQQKDPRRSNLLHQKELFRILRDSGRMPLAVAPLLDELKLIGRPTGMNIIGHMGQRITPSRRVLERMGYLNTPRILQPAIGDLVTEFDGWWSHFAGKSPGDSDDQLMQRVKNVDAMLAGEGTVEIDGQTTSPEEYLAAELKELEKTPLTAEQLSAFVGAMLRFDQTQQAFDLMQQQRETELPAAQAGIIYRRLGKWAEAAEAFQQAWENDVLQLEFRYLAADALARSGDREAGAKQMQTASMMAVNFRIRNALTHRLRELGAQPLAAKEARLLQAVSPIGSFTWYKSCQRRADLETDPATVADLQQTTMLQFAGGWTKEIPLSDLASLHRIHRMRAAAAIEADDFEKAQQHIDRMLNLNRIDPQNGEQLIPALRAAGRDKQADALQGKLIVTSR
>NZ_CP036292.1|WP_145117209.1|159731_160373_-|DUF1080-domain-containing-protein
MRRLFACFLLLFPIVAVAQSPAPESGFTPLFDGKSLQGWEGDANWFRVDDGAIVAGSASETIPNNFFLATTEQYEDFELRLEAKLVGAGQNAGVQFRTRRIPNHHEVSGYQADMGTAGGKPIWGSLYDESRRNKMLAVPDPAAVEAVLKTDDWNRIRVRCQGARIQIWLNDLQTVDYTETDPQIERTGIIALQIHGGKPALASYRNIRIQRLK
>NZ_CP036292.1|WP_145117210.1|160620_162300_+|dihydroxy-acid-dehydratase
MNAPLNKYSSRVTQPKSQGASQAMLYGTGMTSEDMNKAQVGIGSVWYEGNTCNMHLLDLANEVKEGVRAADMVGMRFNTVGVSDGISMGTEGMSFSLQSRDLIADSIETIMGGQWYDGLVALPGCDKNMPGCLIAMGRLNRPSIMVYGGTIRAGKWNGQKLDIVNAFQCYGQYLSGDIDESERQNIVKCSIPGAGACGGMYTANTMATAIEALGMTLPYSASIPAEDPAKKDECRRAGAAIRVLLERDIKPRDIMTRQAFENAMAVIMAVGGSTNAVLHLIAMARAVDINLTIDDFQAVSDRVPYIADLKPSGKFVQEDLHSVGGTPALMKYLLAEGVITGDCMTVTGKTLGENLADVPDLDPGQEIIRPLDKPIKASGHIRILRGNLAPEGAVAKITGKEGLLFTGTARCFDSEEEMLTALEEKKIVKGDVVIIRYEGPKGGPGMPEMLTPTSAIMGAGLGADVALMTDGRFSGGSHGFIVGHVTPEAQEGGPIALARDGDKITIDAEKLEINIDVSDEELAKRREEFVAPPLKATRGTLYKYIKNVKSASEGCVTDE
>NZ_CP036292.1|WP_145123940.1|162642_163395_+|TIM-barrel-protein
MGWCFKPIPSIELAKHCKAIGIEAIEGIPASDYPAVTELGLKISLVGSHGFQNGPLDPENHAMNEAKLREAIDTAVKFGAPSVITFTGMRKTGIDDRQATKNCLDLWKRVLPYAEANDITLVLEHLNSRDDTHPMKGHPGYWGDDVELCVDLVKQLDSPRFKLLFDIYHVQIMNGDIIRRIREYHPLIGHYHTAGSPGRGELNDDQEINYPAVMRAILETGYSQYVAQEFIPTSNDPIASLREAARVCDV
>NZ_CP036292.1|WP_145117211.1|163564_166189_+|hypothetical-protein
MATRTIERIDETHSVGPRVRVDDFVRLGIGVREARVGVIRRAAGDATAAVALDEPTDTRHGFDDRIASIAASTYRLLDPRGRNELMQRVQLLQLESPPAQVKPWWKPRHATVVTQDELRDRFDPSAADDTYLPVGLQAEAGWKTVARRMGLFPFSRRAVWVASAMASVSILIVLPIVIAMSSADDPPSGELTAAATTVSAAPEPIARQLGSAAASPQLTTDFPVAEVDEPAPAAEPVSPFAEAFVVPSESDGLEASPSESEPMPVHRSLPGTAPSSADPLVFVPNVEPSATLEDAPSVAPESPSTPAPITDPESTEPKSLESESIEPMPADAASSDSPMPTADVPTDPMPPVPATPAPIATPVAPPAAAADPAVDPFAQVDLQPAVEADGGLQDSRFPKPSADEIAVATERLARLRADLPAANTDADLVSNIRKLLQTATESEPGSADRWVLLLESSQHLLMMGRGADAQQALLQLTREYQASEVQLRQLLLEPLINGAQTITQKERVIGWALSTSELLLRAEEFDSAATTLRGATTLAVKLGDNDLRVRINLQSDAIKQAKRIAPLATKALAESTPTTASASAANSVGRYLCLYLYDWPQGLPWLKHASTPKLAKVAQMEIDTAAAPDSTLDLVNSWIECAADVRGRGGESILLHARDLVAEAMLESSGLKAKDLERKLAELDAMLPADLRTVAPTPSIAAAPAAAMPAGNLTGMLGRLKADGLDVSALIRYDAGLNLTHDAFSQILDQLGIQAGTISLEFVGLIDLPENSTIRFVTSTGTDKADAVVVAVNNQTVPLSVEGQRNRKAGTVDLPAGSHLVRWQFGGKQLATCHLVVEDDRAKKPLTLRHTPALLEQVLSVAPARLRVNVVRAN
>NZ_CP036292.1|WP_145117212.1|166238_167123_-|IS3-family-transposase
MKYAWIKQHRDSFPIQTMCRVMRVSRSGYYAWCVREPSARKQRTNKIRADVQRVHASSKQIYGSYKVAELMQADAQLESASRNTVAKAMREMGLKSKVHKRFTPTTTVADPTKVPAPNLLDQVFEAEGPNRKWVTDITYLPSANGWIYLAVVLDLFSRKVVGWSISESLATPLVEDALRQAIANRRPDTANLLHHSDRGCQYTSSEYQRTLKTLGITCSMSRTGCCYDNAVMERFFWSLKHEWTKFESFADINDARSSVFEYIEAFYNSTRIHQTLGYRTPNQFEVDHEQSLAL
>NZ_CP036292.1|WP_145117213.1|167119_167425_-|transposase
MPENPRQPRRVHSDEFKRSAVELVTKKGYTIKQAADAVAVAPRSIRDWIKKFDASAIPASVGSSNDALIAENRRLKKALLQAEMERDILKKATAYFAKESK
>NZ_CP036292.1|WP_145117214.1|168001_169426_+|magnesium-chelatase
MSTPSEVPSISNLSELRQSGWKSKTVKHELRDNFLVALQAGDVLFPGIVGYDDTVIPEINLAILAGHDMLFLGEKGQAKSRIMRMLVRFLDEWTPYIDHPELPVHEDPMDPITALGKRLVKELPEDQIKIAWWHRNDRYSERLSPGTKFADIIGEIDPGKLTSGVSMNAEAALAFGLIPRMHRGIFAMNELPELDDLVQVGLFNILEERDVQIRGYPIKFDLDVMILFSANPSTYNRSGKVIPQLKDRIGSIIQTHYPSDRDQGIAILQQEANDDLGGPFPVQVPYFMYEVVEEITKQARRSKFIDHQSGVSARFSLANFRTMVASARQRSVVLGESPAVPRISDLGHIYSSALGKLELDLMGSHQMSERQVLDAVVAEAIQVVFQKYVEQHGTAEIGEIFKKGVRVEVGDMLPSTVYAERLKRVPPVWEKAFEVNASASEPVRASCVEFVLAGLYSMDHISRSQRHGSIEYEI
>NZ_CP036292.1|WP_145117215.1|169628_171329_+|hypothetical-protein
MKKRPGGIIHSYQKFDPAQFPSPTQPPPDLVSSAFEHAMMFGNYRELSEEELARAVKLDPSQIAGLGPSIDMLRQMLEERKRKILETYETAAAQKRARCAYQQSASAVRPPKDLEKAYRRGIAEEQPYDLERLWYQADSDHSPFARGLLGVMQRMNDKLLIAELVSKYEFTGREPMSVPKALEIKEELEKIDELLRQLEEAAKTAQIGIIDMDLLQEFAEPGDLNELEELRQQVENYMREQAERQGLDRDNKTGNYRLTPQAYKLFQGKLLSRIFSDLQASRSGRHPDAVEGDGAVELQQTKPYEFGDSVANIDLPQTVINALLRHGDTRPLQLRSEDIEVHRTRNHPKCATCVIMDMSGSMRYDGQYINVKRMALALQGLITSEYPGDFLRFIEMYTFAKMRHASELIELMPKPVTIHDPWVRLRADMSREDISESQIHPHFTNIQRSLQLARQNLVTTDTPNRQVVLITDGLPTAHFEDNHLFMLYPPDPQTEQATMREAMLCHREGITINIFLIPSWSQSEEDIRFAYRLAESTKGRVIFTSGKDLDRFVIWDYVSNRREIIG
>NZ_CP036292.1|WP_145117216.1|171830_175106_-|efflux-RND-transporter-permease-subunit
MYWLAEVCVKRPVFALMLITALVVAGAVAFPQLGVDRFPNLDMPQVFVRTTYLGAAAEEVESEVSSVIEDAVATVAGIDELRSISANGRSFVIVTIELDRDIDAAIQDVRDAVAGVANLLPPGIDPPIVQKRDLDSSPIMTLAVSGPRSARELYVMADRYVKNVIESSSGVGEVKISGAADRAIQVDIDARRLAAHRLSILQVRDALVRQNAEVPGGLMNEGQRERSLRTLGRISESHRFPDLTVATVGDTAVRLSELGTVTDGTKEVRTLARLNGQPAVLLEIQRQSGENTVAVIDAIKEQLPRSQELLPDDIRVEVIQDQSRYIVEALHEIERHLISGSILACLTVMLFMRSWRSTIIASVAIPASIIATFAFMKWFGFTLNNVTMLALVLMVGVVIDDAIVVLENVFHCIEEKGMAPAEAAVTGTKEIGLAVLATTISLVIVFLPVSFLSSVTGRLLFEFGVTATVAILISMLVSFSLTPMMCSKLLRPIDKPTEDESGKSKKSAAVKSRGGVYSWIEGAYLWMLARALRFRWLVLVVVVLVIASNIPLSQWVRRDYIPLNVDESEFEIRAEAKPGASLLAMQATIDRVEAELDKIDGIEAVMTTVGTGGYGDVNRAKMFVRLQDSRERTFSFGRLWDGLLTGDPKAAFRGNFTQREKMGEIRKRLSPIKDLRLSVRNLTSLRQGAPVDIDFAIMGPDAEKLLEFSDKMKARVKEIPGIVDVYSTLQINNPELLVSIDRQRAAALGVEVREIADTLRVAVGGDDRVSRYLDQSAGDAYDVELRLVGLDRNDIQSISQLYVRTNPMLPTTSANDLVVAAIETGLSGSMTRIDNVVDFEYSQAASRIDRLSRQRMVSVRANIANGYALADRIEAMEQVANEIGLPEGFNYEILGGGRELERTITDFGWTFVLSFIFMYIVLAAQYENMVYPLIILLSLPLAIPFGLISLYWGGETLNLYSALGILVLFGVVKKAAILQVDHTNALRSQGIGRHDAIMQANRDRLRPILMTTVSFVAGLLPLLIATGPGAEERRSIAVLAAGGQTLSLILTLLAIPVLYTFFDDLGKLPGWLMKPTKSEPARVDSASSIAS

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Crispr_ID: NZ_CP036292_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_3

196074-196215

Orphan

Consensus_repeat	Method
ACCTCCGGAACCTGAGGCCCCGAGGCGCGATGAAGAACGATCCCGAAGGGATGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_3

>merge|NZ_CP036292|3|196074-196215|CRISPRCasFinder
ACCTCCGGAACCTGAGGCCCCGAGGCGCGATGAAGAACGATCCCGAAGGGATGCAAGATGGTAGCCGGAGGTCGCCGCACAGCGGCGCACCTCCGGAACCTGAGGCCCCGAGGCGCGATGAAGTACGATCCCGAAGGGATGC

>NZ_CP036292|3|3|196074-196215|CRISPRCasFinder
ACCTCCGGAACCTGAGGCCCCGAGGCGCGATGAAGAACGATCCCGAAGGGATGC	AAGATGGTAGCCGGAGGTCGCCGCACAGCGGCGC
ACCTCCGGAACCTGAGGCCCCGAGGCGCGATGAAGTACGATCCCGAAGGGATGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145117222.1\|189367_189808_+\|ASCH-domain-containing-protein	unknown	unknown	gnl\|CDD\|227269
NZ_CP036292.1\|WP_145117218.1\|177613_178435_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|176506
NZ_CP036292.1\|WP_145117219.1\|179709_180435_+\|outer-membrane-beta-barrel-protein	unknown	unknown	gnl\|CDD\|226163
NZ_CP036292.1\|WP_145117217.1\|175227_176538_-\|efflux-RND-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|273776
NZ_CP036292.1\|WP_145117220.1\|185884_186799_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|379293
NZ_CP036292.1\|WP_145117224.1\|194614_195886_-\|carboxypeptidase-family-protein	unknown	unknown	gnl\|CDD\|349453
NZ_CP036292.1\|WP_145117221.1\|187258_189364_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|350267
NZ_CP036292.1\|WP_145117229.1\|203067_205125_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145117227.1\|199194_200436_+\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|380491
NZ_CP036292.1\|WP_145117223.1\|190363_191842_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293763
NZ_CP036292.1\|WP_145117226.1\|198078_198990_-\|HAD-IB-family-phosphatase	unknown	unknown	gnl\|CDD\|273653
NZ_CP036292.1\|WP_145123942.1\|193522_194503_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117232.1\|209265_209847_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117228.1\|200542_202996_+\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145117225.1\|196751_198122_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|340951
NZ_CP036292.1\|WP_145117233.1\|209843_211502_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145117230.1\|205322_206825_-\|trypsin-like-serine-protease	unknown	unknown	gnl\|CDD\|379142
NZ_CP036292.1\|WP_145123941.1\|182543_185639_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|372468
NZ_CP036292.1\|WP_145117231.1\|207196_209269_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|315987
NZ_CP036292.1\|WP_145117234.1\|211561_213175_-\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|275376

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145117222.1\|189367_189808_+\|ASCH-domain-containing-protein	gnl\|CDD\|227269	COG4933, COG4933, Uncharacterized conserved protein [Function unknown].	7.4091e-21
NZ_CP036292.1\|WP_145117218.1\|177613_178435_-\|hypothetical-protein	gnl\|CDD\|176506	cd08563, GDPD_TtGDE_like, Glycerophosphodiester phosphodiesterase domain of Thermoanaerobacter tengcongensis and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in Thermoanaerobacter tengcongensis glycerophosphodiester phosphodiesterase (TtGDE, EC 3.1.4.46) and its uncharacterized homologs. Members in this family show high sequence similarity to Escherichia coli GP-GDE, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. Despite the fact that most of GDPD family members exist as the monomer, TtGDE can function as a dimeric unit. Its catalytic mechanism is based on the general base-acid catalysis, which is similar to that of phosphoinositide-specific phospholipases C (PI-PLCs, EC 3.1.4.11). A divalent metal cation is required for the enzyme activity of TtGDE.	1.15592e-49
NZ_CP036292.1\|WP_145117219.1\|179709_180435_+\|outer-membrane-beta-barrel-protein	gnl\|CDD\|226163	COG3637, COG3637, Opacity protein and related surface antigens [Cell envelope biogenesis, outer membrane].	6.15567e-20
NZ_CP036292.1\|WP_145117217.1\|175227_176538_-\|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].	2.34795e-52
NZ_CP036292.1\|WP_145117220.1\|185884_186799_+\|AAA-family-ATPase	gnl\|CDD\|379293	pfam13614, AAA_31, AAA domain. This family includes a wide variety of AAA domains including some that have lost essential nucleotide binding residues in the P-loop.	8.83078e-27
NZ_CP036292.1\|WP_145117224.1\|194614_195886_-\|carboxypeptidase-family-protein	gnl\|CDD\|349453	cd06234, M14_PaCCP-like, Peptidase M14-like domain of ATP/GTP binding proteins and cytosolic carboxypeptidases similar to Pseudomonas aerugnosa CCP (PaCCP). A bacterial subgroup of the Peptidase M14-like domain of Nna-1 (Nervous system Nuclear protein induced by Axotomy), also known as ATP/GTP binding protein (AGTPBP-1) and cytosolic carboxypeptidase (CCP)-like proteins. This subgroup includes PaCCP from Pseudomonas aeruginosa, a carboxypeptidase homologous to M14D subfamily of human CCPs. Structural complexes with well-known inhibitors of metallocarboxypeptidases indicate that PaCCP might only possess C-terminal hydrolase activity against cellular substrates of particular specificity. The Peptidase M14 family of metallocarboxypeptidases are zinc-binding carboxypeptidases (CPs) which hydrolyze single, C-terminal amino acids from polypeptide chains, and have a recognition site for the free C-terminal carboxyl group, which is a key determinant of specificity. Nna1-like proteins are active metallopeptidases that are thought to act on cytosolic proteins (such as alpha-tubulin in eukaryotes) to remove a C-terminal tyrosine. Nna1-like proteins from the different phyla are highly diverse, but they all contain a unique N-terminal conserved domain right before the CP domain. It has been suggested that this N-terminal domain might act as a folding domain.	1.95875e-18
NZ_CP036292.1\|WP_145117229.1\|203067_205125_-\|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.	5.21272e-92
NZ_CP036292.1\|WP_145117227.1\|199194_200436_+\|GntR-family-transcriptional-regulator	gnl\|CDD\|380491	cd06267, PBP1_LacI_sugar_binding-like, ligand binding domain of the LacI transcriptional regulator family belonging to the type 1 periplasmic-binding fold protein superfamily. Ligand binding domain of the LacI transcriptional regulator family belonging to the type 1 periplasmic-binding fold protein superfamily. In most cases, ligands are monosaccharide including lactose, ribose, fructose, xylose, arabinose, galactose/glucose, and other sugars. The LacI family of proteins consists of transcriptional regulators related to the lac repressor. In this case, the domain sugar binding changes the DNA binding activity of the repressor domain.	4.00668e-46
NZ_CP036292.1\|WP_145117223.1\|190363_191842_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293763	cd16144, ARS_like, uncharacterized arylsulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036292.1\|WP_145117226.1\|198078_198990_-\|HAD-IB-family-phosphatase	gnl\|CDD\|273653	TIGR01488, Phosphoserine_phosphatase, Haloacid Dehalogenase superfamily, subfamily IB, phosphoserine phosphatase-like. This model represents a subfamily of the Haloacid Dehalogenase superfamily of aspartate-nucleophile hydrolases. Subfamily IA, B, C and D are distinguished from the rest of the superfamily by the presence of a variable domain between the first and second conserved catalytic motifs. In subfamilies IA and IB, this domain consists of an alpha-helical bundle. It was necessary to model these two subfamilies separately, breaking them at a an apparent phylogenetic bifurcation, so that the resulting model(s) are not so broadly defined that members of subfamily III (which lack the variable domain) are included. Subfamily IA includes the enzyme phosphoserine phosphatase (TIGR00338) as well as three hypothetical equivalogs. Many members of these hypothetical equivalogs have been annotated as PSPase-like or PSPase-family proteins. In particular, the hypothetical equivalog which appears to be most closely related to PSPase contains only Archaea (while TIGR00338 contains only eukaryotes and bacteria) of which some are annotated as PSPases. Although this is a reasonable conjecture, none of these sequences has sufficient evidence for this assignment. If such should be found, this model should be retired while the PSPase model should be broadened to include these sequences. [Unknown function, Enzymes of unknown specificity].	5.34411e-11
NZ_CP036292.1\|WP_145117221.1\|187258_189364_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|350267	cd18700, PIN_GNAT-like, VapC-like PIN domain of uncharacterized GNAT family proteins. This subfamily includes uncharacterized GNAT family proteins having an N-terminal GNAT family N-acetyltransferase domain. This subgroup belongs to the VapC (virulence-associated protein C)-like family of the PIN domain nuclease superfamily. VapC is the PIN-domain ribonuclease toxin from prokaryotic VapBC toxin-antitoxin (TA) systems. VapB is a transcription factor-like protein antitoxin acting as an inhibitor. Other members of the VapC-like nuclease family include FitB toxin of the FitAB TA system, eukaryotic ribonucleases such as Smg6, ribosome assembly factor NOB1, exosome subunit Rrp44 endoribonuclease and rRNA-processing protein Fcf1. The structural properties of the PIN (PilT N terminus) 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. Some members of the superfamily 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. Matelska et al. recently classified PIN-like domains into distinct groups; this subgroup includes some sequences belonging to one of these, PIN_17.	5.12448e-14
NZ_CP036292.1\|WP_145117233.1\|209843_211502_-\|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.	1.04631e-76
NZ_CP036292.1\|WP_145117228.1\|200542_202996_+\|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.	3.0939e-76
NZ_CP036292.1\|WP_145117225.1\|196751_198122_-\|MFS-transporter	gnl\|CDD\|340951	cd17393, MFS_MosC_like, Membrane protein MosC and similar proteins of the Major Facilitator Superfamily of transporters. The gene encoding Sinorhizobium meliloti membrane protein MosC is part of the mos locus, which encodes the biosynthesis of the rhizopine 3-O-methyl-scyllo-inosamine. MosC belongs to the bacterial fucose permease, eukaryotic Major facilitator superfamily domain-containing protein 4 (FucP/MFSD4) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.65663e-105
NZ_CP036292.1\|WP_145117230.1\|205322_206825_-\|trypsin-like-serine-protease	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	1.97634e-23
NZ_CP036292.1\|WP_145123941.1\|182543_185639_+\|AAA-family-ATPase	gnl\|CDD\|372468	pfam13087, AAA_12, AAA domain. This family of domains contain a P-loop motif that is characteristic of the AAA superfamily. Many of the proteins in this family are conjugative transfer proteins.	1.62895e-18
NZ_CP036292.1\|WP_145117231.1\|207196_209269_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|315987	pfam13424, TPR_12, Tetratricopeptide repeat.	0.00200031
NZ_CP036292.1\|WP_145117234.1\|211561_213175_-\|FHA-domain-containing-protein	gnl\|CDD\|275376	sd00029, zf-RanBP2, RanBP2-type zinc finger. The zf-RanBP2 domain represents a new superfamily of C2C2-type zinc finger motif, which is characterized by the conserved sequence pattern W-X-C-X(2,4)-C-X(3)-N-X(6)-C-X(2)-C. They fold into a structure composed of two orthogonal beta-hairpin strands that sandwich a single Zn2+ ion coordinated with four cysteine residues. zf-RanBP2 domains are mainly found in eukaryotic proteins and some exist in bacteria and archaea. According to different binding partners, the superfamily can be classified into several families. For instance, the E3 SUMO-protein ligase RanBP2-like family binds Ran, the nuclear protein localization protein 4 homolog (NPL4)-like family binds ubiquitin, and the zinc finger Ran-binding domain-containing protein 2 (ZRANB2)-like family binds single-stranded RNA (ssRNA). Most of superfamily members contain one copy of zf-RanBP2, but some contain several zf-RanBP2 domains.	1.50029e-07

>NZ_CP036292.1|WP_145117224.1|194614_195886_-|carboxypeptidase-family-protein
MESPPMNPRQLLVPLAFLSLAIAGEQLFADDLLSVAADFEGGSVAEVEIDPAAGSIRFMPGGDPARGWPCWWYFRIDGIQPGQAITLQLRGSTATVGNQPPLGASWAMPKRATYSTDGKTWQQTDPGQRDGHIMTYKLTPDASSVYVAWGPPYTPKTAERLATRLSEASPHVEAMQLCRSREDREVPMLHFHEGTRTAEQRFGVWIQARQHAWESGSSWVAEGFADWLAGDDPQAAWLRQHADVYLVPIMDIDNTATGNGGKNAIPRDHNRDWAAKPHWNEILAAQQKVGELIDQNRMDLFIDLHNPGPGDSTFFFVPSRELLKPQAADSTDDFMELAHQRISSIKPSIPMSNKPRVTGSTYHPLWRQISTNWVSLNGNPNTVSVCLETAWNSPTSTPTGYKAVGENLAIATQQFLAKQPKKP
>NZ_CP036292.1|WP_145123942.1|193522_194503_+|hypothetical-protein
MVKDPSPQRYQFRVRASEIDSRTGEYPAIGFVSGTDEKPADLEFASVDTRVAPKGKLAIWLMGHNGGLFERWNEYGIHAIGVSYARGWFGKLAQPQPSDAYARGRIRLEAATGLDFSDELDLLPPDGAAERARQLLLWLSKENPQGNWQQFLADGGSRLRWDKIIMTGASHGSTTAARFAKHQRVDRVVMLCGPRDQDQDWQSLPSATPANRFFGFTHVLDGGWTGDHYCRSWEMLGMNAFGPIVDVDSTTPPYENSRSLITAADVGGDAGRAHGSVTPGRSSPKNEVGKLKFDPVWRYLYTHPVDEVGVATEEDPGCKRVHVKYD
>NZ_CP036292.1|WP_145117223.1|190363_191842_+|sulfatase-like-hydrolase/transferase
MQLLKFVVRDSLALWVLVSICVGFGGFARAADDARLPNVVVFLVDDLGYMDIGANNPDCFYETPNIDALSNTAMRFSDGYAANPVCSPTRYSMMTGKYPSRVDATNFFSGKRSGTFEPAPLNDNMPLEEVTVAEALKTKGYATFFAGKWHLGESEKYYPQNQGFDVNVGGHSKGGPYTGKKYFAPFKNPQMAVESPDGDHLPDRLARDTARFIDAHKAGPFFAYLSFYSVHTPLIGRPDLVAKYKAKGAKVNGQEFGDEEQVFGDQPRKVRILQKHAVYAAMVEAMDEAVGKVLAQIEASGVADNTIVIFTSDNGGLSTSEGSPTSNLPLRGGKGWVYEGGIREPWIVRYPGVTEPGSVSDQPICSIDLFPTVAAAAGVEYQHAVDGVDLMPALRGGSLDRQSLYWHYPHYSNQGGIPAGAIREGNFKLIERYEDGRVHLYDLKSDIGERNDLAAEDPDRVDQMRRRLHAWYKTVDAKFLQQKKNGPKPWAP
>NZ_CP036292.1|WP_145117222.1|189367_189808_+|ASCH-domain-containing-protein
MLFLSIHPEHVKAIVEGRKTVELRKRKPSIDPGSAVVIYATMPKCEAVAVATVEAIQVGEPTMIWRNCGKLTAVSVQAFNDYFDGAGKAVGIHLSSIAVFKEPVSLGELRQRWGGFQPPQQYRYLDSKQQKFITARETTVGGCPLS
>NZ_CP036292.1|WP_145117221.1|187258_189364_+|GNAT-family-N-acetyltransferase
MTDHEIVVRPIETADELDAVKEIYRTQKALLGFFPDEAFQQRADAKQILIAWSDSDAAGYVLFATNQRYEVRITHLCVKPDYGNRKIAKQLIAALVEAYPNRSRIRLNCRVDYEAAGRYRRMGFSELRRFPGKKQGGSELIAFALAINETPLFDALDEPSETATVVCDTMVCIDIEDQDRPHHKASSGLRADWLVDEINLKVTPGIFADLGRQAEPLRSDMISAVKTGWDQVAADHLEVERQLREVRQIMGEPKDDSSASDQRHIAIAAAIEAAAFVTRDEEVLSFREQIQSSLGLRLLPPAEFITEYDAVLNSHRYQYRELSRSGIERRRVASIDEFDLKCFIDSAGGESLKVFRAELIAMLAAPREWEIYRVCSRSDECIALFAIRILDGGARDIQRLRLSRRLVGTRFGRILAEYFADQPLGAWRSGQRRTVTISDRFATPLVLGACSRRGWCQADGALWRLSLPGQWSQDSLSAELSAMSDSGIVPVEFAEQISRSVDIDHNRLGNEVETQQLERLIHPGKVTFGQLPTWVIPIQPRWAQELFDFRLWDLPLFDPETSLVINPDSAYYKSPRQGPSTPFGRILWYVSGDKRKGGGRVRACSTLTKRVQGTVKNLFREFQRFGVYEWRHLMENFKDADAQGLAIEFTSTELFETPITFEVVNDVLESHGMKRQQFISAVLIPDSAFQEIYSRSTQREH
>NZ_CP036292.1|WP_145117220.1|185884_186799_+|AAA-family-ATPase
MAVILFTNLKGGVAKTTNAIAVAECLASSGKRTLLIDADHQCTASELLLGEQALIELDRKKRTLHDLLSEMLKPEFEAKQFDAYVRPSASNIGGGIEDLSVIPCSVRIDDFQTNYAKGGHGFHTWQDFRKLFNANRLQFRRWLKQFAYVIVDCPPSLSLQVKLFLGIADGYVVPCQPNRLSIRGLLWLSDRIQNYRYKTVCLGTLWSMCRGNDRMHKAIIEGAANNHAQLRDLPTPFETTVPLAANIAHAGELTDKQPKTFRAKYGTEFGRIYEQICEELMERVEALESERAEKRRGRPVTARA
>NZ_CP036292.1|WP_145123941.1|182543_185639_+|AAA-family-ATPase
MHPQVAEANDVGLPSLVDWWQKSWSVLWGPPGTGKTYTTGQQVAAVLNDPTERILVVSTTNRATDAAAISIGRAAREAGFDLDDGDILRIGKGASLKSFERERLEAMLRGTETDYLAQIDALAQRLVSVEDFEEKALIRKEIKNLQGSMRDAAARNFLDDNVRVVVGTSFKAISSLCYEEVKEDFGRGNAPFTTVFIDEAGLMSRVAVAALSLLASRRVALVGDSKQLAPISRISRILEPAQGNWLARSGLSHLDNINRAVDGVHVLSEQRRMHSDVCDVVSAFQYDGFLTTAPEVDERAFTLPSTLAEQPRAIWYVLDDDTDDIPSIRAGRGPGNRSWVRTATIKVLKKLFADKSLRSANGLFISPFKAQAKSIHSFFVKNEMDSWMASTVHSQQGSEADIVIFDSVNAGSYGWPFDEWKRLVNVALSRARESIIVISSRAEMEEPYLRPLMRHLSPKCVRRKGNRLSWDDVSVETEFKLPEQIAEKSADYKVEEPVSIGGQLAKRKELRPVLSHEQERLCGLELDGKPRLVRGVAGSGKTVVLAHWLMKTVKRLQDEPDVRIWAVFANRSLQSLIETSIHQEWDKETNGKPFPLSRVELHHIREILDVMLRDVGLNAESYGFEYDDAAAAYLEHASASDIRPRCDALFIDEAQDMGPNTLKLLSAIVKQQDEEDENSRAINIFYDNAQNIYGRSTPKWSEFGLDMRGRSTVMKESFRSTKPITEFALNVLYRLQSPESNPDHKELVTRGLVERTIRGDSDWWNVRFNQVDGPKPKFKQYGNLEQEFDAIGDYCRELIVDHGVQPCDICLIYNGSNIPGWLKRRTAPKLGGLGVELSVQRNRPYQRGNHVLLATTSHSFKGYDSEIVIVPGVDQYKANGVGVLANNLYVAMTRARSVLTMFSQRMNDPNSQLLYEVLGDCLDQLEERPDVETDTSGQDDLFDILDQIGHSHRTWLTEIWNKHGISQEPLQTDKGEIVADPLFSFRVATQRYACFGKQPPRKRIRQRLEDFGIKLVEPGQDVMDSANGEKP
>NZ_CP036292.1|WP_145117219.1|179709_180435_+|outer-membrane-beta-barrel-protein
MLVQLHQNSLSKCLVALGGLLLSVSGMSSFGHAQQPRFFGTSKCDSYCDADGRECCDYDWSGAYVGLQGGWSFLDPNPVAPNHVQEDSDGFSGGVHGGFNRQRGKLVYGIELDYTLTDLDATAPCFNPAFVCGASSDWNASVRGRFGIAFDRLLLFGTAGFAFADYEGFTRLIATGVTYDDEKTLTGGTYGGGLEYAVSERLRVRSEYRYSNFGTEDMSYDSTYTVDPDLHSVIFGASFAF
>NZ_CP036292.1|WP_145117218.1|177613_178435_-|hypothetical-protein
MTATQFLSVLLLAFGQVFFAVDATDEFLANGVTAHRGNSGDFPENTLSAFKSGMEVGADWIELDIFRTKDGRLVVTHDKTTERVGDKNVRVPDSTYEELLAVDVATAFRRRSGNTVEECPAQCIPLLEDVLRLVMKQNRTRVSIQPKMDCVAEAVELVKELKAERWVGFNDGNLQFMTEVKQLAPEIPVFWDRGAGTNIDDDIRIAKQHGFESLVLQYSAITPEKVQKIKAAGLEAGAWTVNDQSMMSKLLDIGVQRIYTDHPSALLALKREL
>NZ_CP036292.1|WP_145117217.1|175227_176538_-|efflux-RND-transporter-periplasmic-adaptor-subunit
MWCRLRFHRRERPPLQKLSPPRSHRPAMHVPTLSSIVSPRAHCIGVAACLSLLVAATGCDSPAAAMKSEPKPEPLETIEAELMTVALQPWPTIVRSQGSLDADEESVVGAKVAGRVAEVHVDLGDYVNVGDPLVTLDQAEFQLKVDQTEAQLEQARAAVGLRAGVPVSELNPENAPPVRQQRALWEEAQSSLKRLESLRVQKAVSEGEYELAAAAERVAEARYASALNGVYEKIAAIGSYQAELSLARNQLTDAIIRSPLEGFIHQRLTAPGSYISVGQSIAVVVRTSPLRFRSSVPERRAQALSLGQQVRLQIESVPEPRTATITRISPMLDQQSRSLVFEAEIENEGQELRGGLFAEAEIVVDDDATGLVVPQSAINEFAGAEKTWKVVDGELVEQEVLIGKRRNGQLEVLQGLQSGDVILRDASQGRIAKIKP
>NZ_CP036292.1|WP_145117225.1|196751_198122_-|MFS-transporter
MPTPEMRRPRLPPREHGCFVDDQHLASPIINTNLDPRFDSPMNNIAVPQWIVRNESGNPLTASLWAVRGLFFLNGFLYATWATRIPAIQSQFQLSHAALGVALMMVALGAVVAMPTAGWLCSRWGSRRVVAISLLLYIAGLPLVALMPSLTAFFIALLLFGVGHGMLDVSMNVQAVEVERRWQRPINSSIHALWSVGGLSGAIAGSVIGLWGLAAGLHFALVSALLSLAIVPIVTRLLIESSTAASDARDEETGAPSQPRGRNRALLLLGAIAFCIMAGEGAMADWSAVLLNQVLGVSEGLAATGYATFAIAMAAGRFAGDRLSMRLGPMNQVRISGLVALAGLLIVVTSSHLALALLGFAMIGGGFATIVPAVFSACGRLDNVPAGVALATVSTIGYFGFLLGPPLIGFVAELFSLRIALGCLSVTTLAAVLLATTLTPRATATDDNSQHDRCAA
>NZ_CP036292.1|WP_145117226.1|198078_198990_-|HAD-IB-family-phosphatase
MSIAVTQSDRFHLDSDTRSELPEPAKGGRAKHYLLASDFDQTLSFNDSGEVLSEMLGLPDFERKVKGLASSHLVQQGGELTYLLLHDPDYRQVRREHLVEAGRRIRLKKNLAPLMDLLDRGIDGHRFTFYVVSASPEEVVRSALEGIVPADRIFGTRLNFDPDSGEISSVAQLTAGYGKVTALDELQSQLGVSWDRIVYVGDGSSDVHVMLHVNRCDGYTIAVSENQHLAPIARRTVLSDNAFSVLIPILEDVMGWTDRTKIRELFEASGLDVQGWEKSQVDRLTILPTDADTRDASSAAAAS
>NZ_CP036292.1|WP_145117227.1|199194_200436_+|GntR-family-transcriptional-regulator
MLCRHSGNVRGIVADTKYRQIADELLADITAGKFQPTGRLPSETQLVRRFDVSRPTAARALRELQNQGLIERRAGSGTFVRQQAAVVEEGQRVIGLLAPEIGSTEILEVICGDIARLARLHDCALLWGREGVHPNVNEAFADPTNAQSVTVGADPIEASRQLCDAFIQRGVPGVFFVPLEHHPDSQNLNFRITDRLRQAGIAVVLVDRDIHPFPQRSEFDLVGIDNFAAGFTAASHLLKLGCNGLLFLAPPQTAPTIAQRIAGAREAVISQEPSARPLQVARFEPDDVDEIEKLIARFRLVADASAADARDPLDAIICSNDRVAATLMQTLAKLGIEVPRDIRLIGFDDVKYAQLLTVPLTTIRQPCRDIAMVAFRSMLDCIEKVVVPPRQYLLASQLIVRESCGAYMKPQPM
>NZ_CP036292.1|WP_145117228.1|200542_202996_+|protein-kinase
MMSDLMKTTDSSATDEGSTAMPELEQTLAHDGASPSAGGDADTAKGTKQSRDLAFAVALLKMGHANVRTLAGAAKSWTTHGNLSLADHLFEQKTISADQRTAVQRRSQQMLTSIAKLDRDARSNGANGNKDPMTSSDRERHWLAQLDPNGKVAKLLGIADTSVLSQDEVQDRQVGSRYTLLRKLGQGGLGIVWLARDQNLQRYVAVKEISREVAPGDVALDHFRREAEITGRLEHPGIVPVYQYGEDEATGKSFYVMRFLGKRTMQDAIAEYHERREAGNDDPMMLHRLLSALINVCNSVGHAHSRKVIHRDLKPENVALDEFGQVTLLDWGLAMINDASGMYEVNGRTEPGDLHSVGSTQVGRVLGTPLYMAPEQASGRLDEVDELTDVFALGGMLYAILTGVAPHQSAIEDAETGSSRSDIMSQIVAGEVVPPIKLVPSVPPELNAICVKALSSKRYLRYESAKALEIEIERFIAGTPVHAYKPPTKQRLKRWMADHPTATQSLLLATSLLLIGGAAIAYTARQGRSALQQARYASAQEFTRELEVNLNFETEGMVRNLHFVSELPLMEAVVASHQGGTAIAPQPDGSMAEVGPVELLNRQAHLFGGLLKANPAYLVAYSCIEEEGGGIRELIRSERSGVGRRVFRVPERDLLAREASERDEEGTQVIHSLRPDDVVLITNDQISENVPVNNRSPLVVSGVQATFDSNGLLFGLNIIELDLRSRLEELFTAVAPERVTIYVTDVAGSIVLQFHNGRVQAVDNASITDEFTQLKTFFAEGATASEFGDGSKVFARRVQLGGSPKAQLGIIAHIQQK
>NZ_CP036292.1|WP_145117229.1|203067_205125_-|protein-kinase
MSSLEPSLLSQIIDDWENATDPPSLDRMLVQIADCSQRDRADAILVDQKYRWARGDSIAAEKYLKLCPDIDSEPELRSELVLGEFRARGGATGLREEFVSRFPDLQADVDRQLSVPSGIDAEADVFGTIVGSVANDSARDTSEFNPAPLSLDDFELQRCLGQGGMGSVFQAIQKSLNKPVAIKMLRTNNAPQRLVDRFLQEARVTASLQHPNIVSVHGVGRCPDGGYFLVMDLVDGQSLQDELSEGPLDVRSAAEIVRDAAAAVHYAHTRQLIHRDLKPSNIMRHRDGRVMVVDFGLAKLLADSEHQMTVDGAVLGTPSFMAPEQLESKRGSVSAVTDVFGLGGVLHALLTGRPACQGDSVMQTIAELMSERPIQPPSKLRAEIPSEIDAICLACLQKKPSQRPATAAAVQQRLADWLKSSDASPVDSHRPTRSRWLAPAAAVVAIALVGAALFLPSRMSLDSTASIDPTNTAANPALDVPPILADRDVQLTWNLQVAKEPNGVELAPFQSAIKEGDRVRIDVTLEEPRYVYAYWIGSDGTAQWIDSDGPPNHPVSRISLPSTEGQVFPISGPSGMEICVLVTRSEPLDQPERLVNDFSIEAFPSLPELRFALADGRAYQPPATDTSQSENQEASLAMLGGPSRVIGRAESLAAGSAGSVLAKWRSQWPRDVGYVHYLAIPHLAH
>NZ_CP036292.1|WP_145117230.1|205322_206825_-|trypsin-like-serine-protease
MKKVSWKKNLALMSLAALMSTSTTSANEETGKPVSLPVHADQALAALQPGSGPIDLNAKPIPKGLGALLGQASRGPAASVFPKIAPSVVVVRAGGGYGTGFIVDSDGWILTNNHVIESAGIDIGTASRYAFIHFGDLEDGMMTLNQQASPALVYAASPEKDLALLKLLAVPEGRELKPIAFAAKNATPGTDCITIGHPKRGVFWSVRSGEVVGIAKYPHDMIDTVMTQMVMASDAKQSFAKSLSQSRPRKALLSTCGINPGDSGGPLLNNDGELVAVNFAIPTSEKDSQVNLDKFSYHVHLDEVKEFTANRPEKSEVFQPNYWPPAATSDFLDVDDDDVYETWRFSIDDETPFTGVVVDLDSDTPANFIEDYKAGKQDRKQFECEFALALMPNNRVFYDRDNDGEFDLILTDVDENGFSDLTIAKNSNGWEKIDSKEQRMFDPTVFQDAKLQERFKVLVMSQTKNPAGTAPDAQPQEEAKPETEASPADSAPAEAADSKK
>NZ_CP036292.1|WP_145117231.1|207196_209269_-|tetratricopeptide-repeat-protein
MIRQPIFAILLAVLSQVVTGTLCQFCHADEREAANEILILADRARIEKRFDEAEPYALQALDVAEQLADPGMLIANANNMLGLIDIDRDRPAEALTHFQSALAALEAVKDAFDPSVYAPNRDAMLTSQGIAAYRSNNFEVALESLQTQLTLRIEEGGQNDARLITTLNSLVTVNSELKQFDDVIANLEQIIAIQKVVAGLESAVVAAATDRLATQLETHRGPAAALPYRQESLRLIESALGPIHLEVINSRYRLAITLESEEKYEEALIENTLAIEAAEKLMGPDSNSYQNLLTHQLVLLEHLEKPDAIQAMQQRIDRIASISKWNEKLAENGEAARADKLDEAMQRLEELQKDAAVFGEVSSPMASIKFHEAALLGIGDRPQEAAEAIREGIAIEQQMLSENHPNIAKSWMLLARFQRAFEQPAAAAESYRAGLDSNEKSGFPDQILKQELLYSLGIAETERGQALESMQALDKCYSLRRELELPYDVRDADIGNRFGVYHANVSGPAKALTFLNRAREILLEVAPDHALLGTVNANIATMNEALANQATTEESSGVMPDVAAMAPAEPTPPALPSATSDAMLDESASGNASASGRDWFWLVIFCIVAAYYAEKRGYSLFLWVFLTLTTSIIVALSVLAILPNRKLQKRRNKELRQLEKLLATTTAVASPATPGAVALDVSIGDQITQN
>NZ_CP036292.1|WP_145117232.1|209265_209847_-|hypothetical-protein
MKFNVKFQIPRMSLWNSIFGKRLDFAGKGDVNFQETAIVVCGDLPKFRIPFISQFYTALLTERTTRTVPYARITKYRTTGRWVSLGLLKILFLLLWFLGVAGLLFAGMEQSNPVLQIVLGILGFVIVPLIILMFGRATHYVTYSLPSGKQSQFACRVAPTSSENMEMFSNRLTEYQTAATAFAQTDSTGATTS
>NZ_CP036292.1|WP_145117233.1|209843_211502_-|protein-kinase
MTTATMPDKPDLDNRGAPPPERKIGPYMLRQEIGKGAHGTVYLAHHVDAPETKVALKVVENRGNLDRLLMEPEILSKLRHPGIVGLLDFFIDNDRLIVALEYLDGRDLKEYAEQHGTFSAAEVREFLRQMASALQHAHAAGILHRDIKPANILVITSDDGQPRDVPRFVLTDFGISRVADGIQVSRNTGGTYQFMAPEQLRGRATTQSDLWALGVVAYQMLTGDLPFVGETVKELASEVFYKTPVPLEDILGNSNDDQLATIIYGLLEKQLSTRTGSPAELLKLLGDQSSPSTGELKQGNDHKLTIDDQTNRKIRLCTIGCVISAIFWAGPLMVPSTVIVLLGLWLFYTGQRAAFFKQQWGRSLIYTVLGLLTLVLGHLVSDAVLPAMLAGLQKGGIQIDDGTLRIGMLASVVFSLIFVPLTCYLFSRIRYLQRGRDLRRSITENAGDSSMQLKILETMAQERSEDLGVRQKYAETLLANDQVKQAAVEAKLMLDDDPYNMEAGMLLAHSYFELRLYQEAIGVCDSFLAVAGYCFEFRELRDQSANQLGVQS
>NZ_CP036292.1|WP_145117234.1|211561_213175_-|FHA-domain-containing-protein
MSASLPAGEAICPHCQSENKADAVRCVQCRRVLKIEIGPTAEPEQDGTDQPQTCSHCGETNLADAVRCSGCRRVLQSNYGPTQEGDQTQSDAAIGPGASPLPAFDIPTVLPPKQDELPPAIRKHRLALMLATIVVTGLLGFAFRIDRTAWLQSWSDDCEQAFSNSGEASSTHWTTLPSGLVERVKVYLVADSPGDIQVASDLANRLPLEIVSEEAIGIQQWREATYPQIQESGGNHLSVVITNDSAQLRLAVLYQMRTQRRLPAFEYVASLGIMDLYGPILLLFSLCSAFAYGVDVWNIHQYRNQRRIAFSGYQAKRAQWLFQVQTHMASAEQATAGGDIETGKHLANEVLRVAPGFPDAVALLTEQQSPSDASSSESQTSANRLFSQLYLQVAGSPYAYHAPRSAKIVRVGRQRRKPGQGPEEGNDFVIRVPGSEAKTRKLSRQHLEIHRIGNDYFAIDRSAVGTHLNGRRLSNDQPSLLATGDRLMIGGVLTLEVLIRREEFIGASAVQTEVEMTPYNNPGIVVDASVGDLVTIE

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Crispr_ID: NZ_CP036292_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_4

557400-557503

Orphan

Consensus_repeat	Method
CGCGGTCGATGTAGCGATTAAAAACGTTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_4

>merge|NZ_CP036292|4|557400-557503|CRISPRCasFinder
CGCGGTCGATGTAGCGATTAAAAACGTTTGCGGTCGCTCGTAAAGGAACCGTTCGTTTCACCACGCCTGGCTAGGCGCGGTCGATGTAGCGATTAAAAACGTTT

>NZ_CP036292|4|4|557400-557503|CRISPRCasFinder
CGCGGTCGATGTAGCGATTAAAAACGTTT	GCGGTCGCTCGTAAAGGAACCGTTCGTTTCACCACGCCTGGCTAGG
CGCGGTCGATGTAGCGATTAAAAACGTTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123966.1\|566676_567558_+\|EamA-family-transporter-RarD	unknown	unknown	gnl\|CDD\|225510
NZ_CP036292.1\|WP_145117455.1\|549032_550454_-\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293774
NZ_CP036292.1\|WP_145117452.1\|546630_547026_+\|30S-ribosome-binding-factor-RbfA	unknown	unknown	gnl\|CDD\|234787
NZ_CP036292.1\|WP_145117457.1\|552547_553786_-\|DUF1573-domain-containing-protein	unknown	unknown	gnl\|CDD\|377880
NZ_CP036292.1\|WP_145117461.1\|559057_560368_-\|beta-ketoacyl-[acyl-carrier-protein]-synthase-family-protein	unknown	unknown	gnl\|CDD\|238430
NZ_CP036292.1\|WP_145117453.1\|547095_548133_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|172341
NZ_CP036292.1\|WP_145117458.1\|553858_556240_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145117463.1\|562039_562918_-\|Rpn-family-recombination-promoting-nuclease/putative-transposase	unknown	unknown	gnl\|CDD\|372314
NZ_CP036292.1\|WP_145117456.1\|550617_552510_-\|cytochrome-C554	unknown	unknown	gnl\|CDD\|372604
NZ_CP036292.1\|WP_145117454.1\|548253_549006_+\|YebC/PmpR-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|234640
NZ_CP036292.1\|WP_145117462.1\|560610_561780_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117464.1\|563099_564896_+\|elongation-factor-4	unknown	unknown	gnl\|CDD\|235462
NZ_CP036292.1\|WP_145117459.1\|556215_557358_-\|undecaprenyl/decaprenyl-phosphate-alpha-N-acetylglucosaminyl-1-phosphate-transferase	unknown	unknown	gnl\|CDD\|133463
NZ_CP036292.1\|WP_145117467.1\|569951_570752_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377585
NZ_CP036292.1\|WP_145117450.1\|541965_543501_+\|transcription-termination-factor-NusA	unknown	unknown	gnl\|CDD\|236410
NZ_CP036292.1\|WP_145117466.1\|568541_569624_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225832
NZ_CP036292.1\|WP_145117451.1\|543664_546559_+\|translation-initiation-factor-IF-2	unknown	unknown	gnl\|CDD\|235401
NZ_CP036292.1\|WP_145117465.1\|567645_568386_-\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|181382
NZ_CP036292.1\|WP_145117468.1\|571010_572564_-\|2-isopropylmalate-synthase	unknown	unknown	gnl\|CDD\|234864
NZ_CP036292.1\|WP_145123965.1\|564969_566124_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123966.1\|566676_567558_+\|EamA-family-transporter-RarD	gnl\|CDD\|225510	COG2962, RarD, Predicted permeases [General function prediction only].	8.4503e-82
NZ_CP036292.1\|WP_145117455.1\|549032_550454_-\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293774	cd16155, sulfatase_like, uncharacterized sulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	4.49795e-147
NZ_CP036292.1\|WP_145117452.1\|546630_547026_+\|30S-ribosome-binding-factor-RbfA	gnl\|CDD\|234787	PRK00521, rbfA, 30S ribosome-binding factor RbfA.	3.05792e-34
NZ_CP036292.1\|WP_145117457.1\|552547_553786_-\|DUF1573-domain-containing-protein	gnl\|CDD\|377880	pfam07610, DUF1573, Protein of unknown function (DUF1573). These hypothetical proteins, from bacteria such as Rhodopirellula baltica, Bacteroides thetaiotaomicron, and Porphyromonas gingivalis, share a region of conserved sequence towards their N-termini.	3.03034e-17
NZ_CP036292.1\|WP_145117461.1\|559057_560368_-\|beta-ketoacyl-[acyl-carrier-protein]-synthase-family-protein	gnl\|CDD\|238430	cd00834, KAS_I_II, Beta-ketoacyl-acyl carrier protein (ACP) synthase (KAS), type I and II. KASs are responsible for the elongation steps in fatty acid biosynthesis. KASIII catalyses the initial condensation and KAS I and II catalyze further elongation steps by Claisen condensation of malonyl-acyl carrier protein (ACP) with acyl-ACP.	5.19577e-92
NZ_CP036292.1\|WP_145117453.1\|547095_548133_+\|hypothetical-protein	gnl\|CDD\|172341	PRK13808, PRK13808, adenylate kinase; Provisional.	1.04186e-09
NZ_CP036292.1\|WP_145117458.1\|553858_556240_-\|hypothetical-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.	7.6982e-05
NZ_CP036292.1\|WP_145117463.1\|562039_562918_-\|Rpn-family-recombination-promoting-nuclease/putative-transposase	gnl\|CDD\|372314	pfam12784, PDDEXK_2, PD-(D/E)XK nuclease family transposase. Members of this family belong to the PD-(D/E)XK nuclease superfamily. These proteins are transposase proteins.	4.95893e-48
NZ_CP036292.1\|WP_145117456.1\|550617_552510_-\|cytochrome-C554	gnl\|CDD\|372604	pfam13435, Cytochrome_C554, Cytochrome c554 and c-prime. This family is a tetra-haem cytochrome involved in the oxidation of ammonia. It is found in both phototrophic and denitrifying bacteria.	2.9032e-16
NZ_CP036292.1\|WP_145117454.1\|548253_549006_+\|YebC/PmpR-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|234640	PRK00110, PRK00110, YebC/PmpR family DNA-binding transcriptional regulator.	3.31024e-134
NZ_CP036292.1\|WP_145117465.1\|567645_568386_-\|methyltransferase-domain-containing-protein	gnl\|CDD\|181382	PRK08317, PRK08317, hypothetical protein; Provisional.	6.78485e-21
NZ_CP036292.1\|WP_145117464.1\|563099_564896_+\|elongation-factor-4	gnl\|CDD\|235462	PRK05433, PRK05433, GTP-binding protein LepA; Provisional.	0
NZ_CP036292.1\|WP_145117459.1\|556215_557358_-\|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.	1.64792e-67
NZ_CP036292.1\|WP_145117467.1\|569951_570752_-\|hypothetical-protein	gnl\|CDD\|377585	pfam05991, NYN_YacP, YacP-like NYN domain. This family consists of bacterial proteins related to YacP. This family is uncharacterized functionally, but it has been suggested that these proteins are nucleases due to them containing a NYN domain. NYN (for N4BP1, YacP-like Nuclease) domains were discovered by Anantharaman and Aravind. Based on gene neighborhoods it was suggested that the bacterial YacP proteins interact with the Ribonuclease III and TrmH methylase in a processome complex that catalyzes the maturation of rRNA and tRNA.	4.78342e-18
NZ_CP036292.1\|WP_145117450.1\|541965_543501_+\|transcription-termination-factor-NusA	gnl\|CDD\|236410	PRK09202, nusA, transcription elongation factor NusA; Validated.	9.84957e-141
NZ_CP036292.1\|WP_145117466.1\|568541_569624_-\|hypothetical-protein	gnl\|CDD\|225832	COG3295, COG3295, Uncharacterized protein conserved in bacteria [Function unknown].	0.000148186
NZ_CP036292.1\|WP_145117451.1\|543664_546559_+\|translation-initiation-factor-IF-2	gnl\|CDD\|235401	PRK05306, infB, translation initiation factor IF-2; Validated.	0
NZ_CP036292.1\|WP_145117468.1\|571010_572564_-\|2-isopropylmalate-synthase	gnl\|CDD\|234864	PRK00915, PRK00915, 2-isopropylmalate synthase; Validated.	0
NZ_CP036292.1\|WP_145123965.1\|564969_566124_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	3.03133e-48

>NZ_CP036292.1|WP_145117459.1|556215_557358_-|undecaprenyl/decaprenyl-phosphate-alpha-N-acetylglucosaminyl-1-phosphate-transferase
MLDLRSLLFLLAVTVLPAAIISWIVVAVVRRFAEPLGLVDRPGERKVHTTPTPLGGGIGIWAGIIGTFLAGSITVWYLIDLPTIANLLPASVLEHVDGLRFRTRELWLVLGAGTVLTLLGLVDDWRGLPATLRLAIEFAVAIASVLVLGYGLTAFIPVPLVTSTLSVIWIVALINSFNMLDNMDGLSGGVAAIIAAMLAAVMLLSPDPDTQQPQFFVAALLLVVVGSLLGFLWHNRPPAKIFMGDAGSYLVGFLIGIATLAATYAGYQGSERPHGVLAPLCVMAVPLYDMTTVLWIRIREGRSPFVADKSHFSHRLVDLGLTKVQAVLTIYLVTGTCGLAALLLGRVDSQAAIIVVGIVLCMLALVVILESTGWRRKNKD
>NZ_CP036292.1|WP_145117458.1|553858_556240_-|hypothetical-protein
MAKKKQRLTTTKPKPPAPSHRDGQSDASAAPWPPVAYAGTLARFGIAALLIATLMAPADSTAVEQGSATYLSLLTLPLAIAAFFYWPAGPTQGRRTELLLLALVVWVGLATWSVAGRGNVRFAINEFWVWLGCLATYAAARRVIVTTAQKQCLAIVLLASLTTLAVHAIHQKYISIPASIEQYRQDPDGQLRLAGLDAPAGSALRYQYEGRLFAAESMATFSLSTSAAVILFMGLAIAGGMILWRQKLQLTQWQTVAAAVATAIFAWGILTTGSLIVLILSIAAAITMLACRFIGGALSNVALRSAKGSESERTFAERKGTLAPRLAGAVAVACALGGTCLGAAITHSPALLAKFPLSVQFRFQYWASSFRMLADQLWFGAGPGNFQSTYPRFKAASMSEMIADPHNFLLESATAAGLPVGILCLAILWSLAAAWSRSNLEEHSTEPTNDQEGPSRERDSATSGNCDWAICGGALLSVVSVWFLGPWFGVAPDIEPYLISIPMAATFVYFMAGWFGTDVNWEAIAWPGCFAVLAALLFSGGWTTPGIAIPLWALIGAISSREMPAEANARTPRQLSLLAGLGLLALFSSTTLTPVMQTLALTQTAGDRIARGDAPTAIQLLRQATEADRWDAAPAMQLESVLTGALMQQSTAAARQEWQQAKDEVLRREPGNPRAWQRLAESQLRIYHRWGDRPDLQAALESSEIALQLDPTSIQITAQVAVFAAAVGDKDRSEAAWQRAEQLTAVNQNTESEWNLLQVLPADRPLDGRKPLESISVQQAWANRNQGPTVEND
>NZ_CP036292.1|WP_145117457.1|552547_553786_-|DUF1573-domain-containing-protein
MRLLAIIALALIAGISLGKLTGSRQTTESIDHFGPFTEVEDFDLEQLPQYLSSLIPDNVGQIELIGEKDFDFGVMHRNTEGEHAFKIRNVGTGPLRLEVTGSTCKCTVGELENESIAPGETSEIKLTWKTRSNTTEFAQTATIKTNDPNNVEVKLTVHGTLVETLLTEPTDWSVGNVTSGEPIDLEFTAYSYADAPIEIVSAQFLDETVQALTEVDWTVRKPDEKTDGKHHAALQAFEFKVKVKPGLRQGSLNHVLRVHYENDDLDEDSPSFDMNLSGNIVGPLRLLGGSKLEQSDKGDGGGYRFNFGTVRQGDPGNERIHLVIRGKEYEDLVVKVGEIKPDNVFAVSLGEENRRGTLRSIPIDIQIKPEAPLGIVRGMKSLDTGYVMLEPQNSNLSPLKLWLTVEVTAVDN
>NZ_CP036292.1|WP_145117456.1|550617_552510_-|cytochrome-C554
MHRTQLAILTTICCLLLNSGCDRSTSVVQETEEPARSVDRAADPAPAATESVASQTAEPQQAKPVEIAKNQPAETPAAVEPTASDEPMSPTPAEPAAEPPAAEPTSLVAAVPTPAPAPTPAAAPTPAAAPTPAEEATDAEEPAANEPAEAPAAELTASPAADTEVDDRWKQWPKPSAVMLFTGEQHGYIEPCGCTGLENQKGGLARRHTLIKEIQTLGWNVVPMDAGNQVRRYGQQAGIKFQTTVASLRTLGYRAVGFGPDDLRLDVGLLLSEAASDPDAPLQFVSANVTLLDPELLPSTRVIETGGKRIGVTSILDPKTVAQPLSDEILVDPVAPAVKASIAKLASENCDYKVLMYYGGNSAEEDINTMGAQLDGIDLVVIANEFGEPTYKPQKVQGSNTAEMILTGHKAMYACLVALYDDGSPSRYARIPLTDALEDSPAMLQSLAVYQDHLKNLGFSGLGLNPIPHASGNKFVGSQKCGECHTTAMEIWEGTPHAHATESIVRPPNDRGDIARHFDPECLSCHVTGWNPQGYYPYLSGYLSLESTPQMVANGCENCHGPGSQHVAAEEGDIDADDDLLEKLRNAMRLPLSKAREKCMECHDLDNSPDFHKEGAFDEYWEQVKHIGKY
>NZ_CP036292.1|WP_145117455.1|549032_550454_-|sulfatase-like-hydrolase/transferase
MMGYAQRVRRIGLVAALLFAGTGFAKPTAAEQQPNFLVIVSDDQRPDTIAALGNSVIETPNLDQLVREGMTFTRASSAFPLCVPSRAEILTGATAFHNGVPYGGGRLKKGQVFWADALRNAGYQTWYCGKWMNDGAPKTRGYEETSGLFSSGGAGPLGREPRYGRHNRLITGYRGWTFKSADGTPELEKGIGVVGETSKYIADGAIELLQRKTDKPFFMHVNFTAPHDPLIIPPGYAGKYKPSEMQVPANLLPKHPFDHGNIDGRDEQLLPWPRTEADVREEIAAYYAVIDDMDAQIGRILAALKASGRYDNTVILFTSDHGLALGSHGLMGKQNMYEHTIGVPFIIAGPGIPKNQRTAAQIYLRDMYPTTCELAGIPIPETVESKSIVPILRSPDTEIYPAVFGYYKDTQRMIRTSRWKLIRYPKVGRTQLFDLENDPDELVDLSGSSKHQELASRLGGQMDQWFQQQNEKH
>NZ_CP036292.1|WP_145117454.1|548253_549006_+|YebC/PmpR-family-DNA-binding-transcriptional-regulator
MAGHSHWAGIKHKKALVDNKRGKLWSRLSKAIIVAAKLGGGDTDTNIRLRKAIDDAKAVSMPKDNIERAVKRGTGELDGGNLEEILYEGYGPGGVAILCDVLTDNRNRTAPEMRVLFERNGGNLGTINSVAYLFDRKGLMLFAAETDEERLTEVALEGGADDIQRSDSGGWEVTCPPESFSDLLAAFEAAELQPELSEVTRLPQTTVEVEGSVAQQAMRLLELLDEHDDVQSVSTNLNITDDALGDEADG
>NZ_CP036292.1|WP_145117453.1|547095_548133_+|hypothetical-protein
MSTTNRSARITKLFTLLKKRYKPLPPSAGRNLFEHFLYACLLEDGSQEAADEGIARLEQDYFDWNEVRVTTVSELAESFPRLPNATEAASRLKKNLHALFETYYSFDIEEMKKQNLGKTIKDLSEFPAMTSFVLAYIVQQGLGGHAIPINAVGMDLFYYCGIINDAERESDKVPGIERAIPKSKGTEFSSLLHQASLDFASNPQDPDLLKLILQINPDAMDLLPGKKAPAASPAKSKSSSKTASAKSAAGKAASTKSAAPKAAPVKKAAKKSTAPSPPDKAPLKGIAASIKAKKASASQPAKATPAKKGTAKSKTAKGAGDKSDADEATKPARSSTKKLAKKKPR
>NZ_CP036292.1|WP_145117452.1|546630_547026_+|30S-ribosome-binding-factor-RbfA
MTSRRQLKAAEAIREVVATSILTELRDPRVKDVTVIGVEIDPDMRNAKVRVSVMGDEKQQTLTLRGLQNSAGYLQSKIAARIDTRYTPRLTFKIDKGLNNALEVSRILEELRKETPPASDDSATDGSEDPS
>NZ_CP036292.1|WP_145117451.1|543664_546559_+|translation-initiation-factor-IF-2
MAVRIYALAKDLKIDSKELVQICNKVGVTGKGSALASLDDDEVEKVKKHLSQLGAPKVAKAAPKEDVRPVRGAGPLGTGLKKTGPVAELKSRPKTAAEEEVEAAPVVEAKQPPAETKPVAEPAAPVEPPAAPIEVAKKPAPAPTPPPVEEPPKPVRASAKSEPNKPVMPAANAPLRREAIRGGSGSRIRDIGGRNRSGGGKPSGNSDGERTGGGKKRGPVINLAAVPKSPARQQRPAAGEAPAQKPEIRLSKDVIAGHKQGMKASLEKLVQDDVDKKAESNKSKGKVGGALSSFTGTGNERGRGGKGADVEEERTKKKGIAGMASARADRNKGRRGGRRDIERSFGHGDDRRRRRTITRTGRNTAAPRKESVVLELPCSIRSFSEAAGVSAAQVLKALMGMGMMMNINAQIDQSTAELIAAELDIDISFKSQTSLEEELIEKIEDRADEEGDLEPRQPIVTFLGHVDHGKTSLLDYLIGTRIVKGEAGGITQHIRAYEVDKDGRKITFVDTPGHEAFTEMRARGANVTDIAVLVIAADDGIMPQTEEAISHAKAAGVPIVVALNKMDLVGVDPNRPMTQMTEHGLTPSEWGGDVEVVRTSATTGMGMDELLDTLLTVAELNEYKANPNRDALGVCLESEQQADRGVIAKFVVQNGTLKVGDVVVCGPAHGRVKALTDTLTGEAMDEAGPSTPVNVTGLDQPPGAGDRFHVLDNIAEAREIAETREFDSKSQNLSGITTKVSFEHFQQLLQDGQLGKAEERAKLNLIIRADMKGSLEAIDKEIAKFDHPEVEIRVLQRSVGGITVADVTLASASDAVILGFNVIPDEAARGMIDDRKVEIRRYDVIYKMTDDLKAMIEGRLKPEERVVELGRAVVKQVFSISRVGVVAGSYVAQGSIERGCRIRVNRDGRTIGDYPLDSIRRHKEDVKEVPRGMECGIRLSGFNDIKQDDVLEAYRIEEFARTLD
>NZ_CP036292.1|WP_145117450.1|541965_543501_+|transcription-termination-factor-NusA
MNPQDLLRYVDSLHREKNIDPSLLFSAIEAALATAARRHYGEEADIVVRIDHDSGKIHAEIDGAPLDQDQVGRIGAQTAKQVIIQKVREAERDALMAEYREQIGQMVSGVIQRADGGVATVQLGNVEAILPRSEQISGESLHANERVRAVVFEVRATGNRVRVVLSRTRPQLVKCLFEQEIPELSEGVIAINSISREPGYRSKVAVSSTDSQVDPIAVCVGYRGSRIKSVREELAGEHIDVVRYSDDPQILIPNALQPAEIEQVLLCNMIGRAIVLVQEDQLSLAIGRRGQNVRLASKLCGWDIEIMTGGELEEQIERAVTGFSQLEGMTEDLAQQLVEQGYLSYDDLSVIEPETLMQMGGLTAEQVDVIVEQAETQAEEAEAAATEERKKRKQEREAAANAAASGEQPPAAEEQVAEGTESEESEDSAAEVSEETQQGDGAESPAAEEAGADGEAEASVEEVENVIVESEPIDESTEQDSDNKNVAVENINEEGEAEQLASDNVEDPDKA
>NZ_CP036292.1|WP_145117461.1|559057_560368_-|beta-ketoacyl-[acyl-carrier-protein]-synthase-family-protein
MRDSVSPRRVVITGVGLISPLGNQVEAVWEALRDRKSGVDLLQALPSDAMSISCGAEARDFTGSISEFGPLDKQLQRAIKKGLKLMCREIEMGVAAAQLALHDSGLSSDVRDPDRTGVLYGSDYIMTLPEEFAAGIRKCQDAEGRFQFERWSELGLPEVNPLWLLKYLPNMPASHIAIYNDLRGANNSLTLREASPGAAIGEAVSTISRGIVDAMVVGATGTRINPFRTLHVVMQEVLAGGSENPAGLSRPFDKDRTGSVLGEGAGAFILEELEFAKARGAEILGEVVGFGSGTAGATAGPQFIQTAMANALRGAMRNSDTSVGHVNAHGIGTPDGDIQEAAAIVEVLGPDTPPVVAAKGNFGNLGAGGGMVEAIASIQALSEGSLWPTLNYETPDADCPINVVSSNDVPAGDNFVSLNVSPQGQATAFRIAKFAG
>NZ_CP036292.1|WP_145117462.1|560610_561780_-|hypothetical-protein
MFQKTLHASLTIALAIGFATSARSLYAQVTPPPTTGGLSTPPSMQRAPATTAATSVSGQLPRDANQEFRQYDLSRYTNNLSKIDKPEQAVVDWVLRETGTDVWFSEPFGFLSTNRNMLTAYHTPEMQAVVKKMVDRFVNGPTDPQILKMRLLTVSSPNWRARALPLIQDVNVQSPGVQAWLLTKENAAVLISMLSSRTDARESQNSQMTIYNGQTQSLSSTKGRTYVRTIRQASTVWPPYEPEISEVHEGYQLEISPLLDTDGKTIECVIRAQIDQVDKLVPVGIDLPLPNGQSHRTQIEVPQIVSWRLHERFRWDSDMVLLLSCGVIASPDRQTSSNPLLNLDRFIGNTPGRADALLFITFGGRAGEGLAPAPAPQAAVAGSISRGRY
>NZ_CP036292.1|WP_145117463.1|562039_562918_-|Rpn-family-recombination-promoting-nuclease/putative-transposase
MALGISPLVDFAFKMIFGSPESAQALIGLLNAVLDRDSPITEVEILNPFNYQEFADAKQIVLDVRARDDLGRSVNVEMQVARASGLLQRMTYYACSLYTDQLERGNEYWTLRPAISICFLNDWLFRDTAQQHHRFEQTDRASGRRLPAGIEVHTIELPKYNLVTETISRASRIEQWVFFLLRADRYSAAELQAMLPGLEFHAAISVVERIASKTEDRVMYDQREKAIRDQQWLLSSARQEGEQAGVLAGQIQLLQRLLQQPEQPLEELLQLPTEKLTAQHTDLQSQARLRNT
>NZ_CP036292.1|WP_145117464.1|563099_564896_+|elongation-factor-4
MKHIRNFCIIAHIDHGKSTLADRLIQSCGGVSLREFQDQLLDSMDIERERGITIKSNTVTLDYRAPDGQDYLLNLIDTPGHVDFSHEVRRSLMASDGALIVVDASQGVEAQTVANLYLAMEYDLEMLPVINKIDLPAADVDRAREEIDADLGLDPFAAIPVSAKTGVGIEDVLAGIVEHLPAPTGDPEAPLKALVFDAHFDKYRGVILQVRVMEGTLKPRDIIHFMHTDRDFKVDELGYNQLKLVPRKQLSAGEVGYIVAGVKSVQDIEIGDTITLADRPATEPIPGYQPARQVVFSSVYPMSTDEYQDLTKALDKLAINDAALTYEKDSSAALGFGFRCGFLGLLHLDVIQERLQREFDIGLVISAPSVKYQLTMTDGSTLEVDNPSYWPDPMKIQSAAEPYIKATILTPEAYVGPIMELCRDHRSESQTMNYLSAGRVEVVSEMPLGEVLFDFYGKLKMITRGYGSFDYVPIEYRTTDVVKVEILVNKEPIDALSYLVHREKARTRALHYCEQLAEAIPRHQFKIPIQGAIGGTIIARATIQPYRKDVTAKLYGGDVTRKNKLLEKQKKGKAKMKQFGSVNIPQKAFVSVLQADKD
>NZ_CP036292.1|WP_145123965.1|564969_566124_+|Gfo/Idh/MocA-family-oxidoreductase
MHGVTGRMGTHQHFVRSILAIMRQGGVRAANGEMIQVTPILLGRNETKLRHLAEVVADQEIGTQVAWSTDVAAVLTDPRVDIVFDASSTQMRASIVRQAAQQGRAVYCEKPIAVDVSQAMVLAELCESAGIKNGVVQDKLWLPGVCKLRTLRDGGFFGDILSVRGEFGYWVFTGHDPDRPAQRPSWNYRREDGGGMMLDMFCHWQYLLGDLLGPIDRVLAHATIDLPERIDEAGNPYACTADDSAYAIFVTESGITCQFNCSWATRVRRDDLLTIQIDGTKGSAVAGLRDCWVQEMAATPRPVWNPDIPQPIDFHSGWQKLPDTTTYDNAFKVQWELFLRHVAADEPFPWTLRRGVDGVALAEAGQTSSAEQRWVSLGGSPSSI
>NZ_CP036292.1|WP_145123966.1|566676_567558_+|EamA-family-transporter-RarD
MCAVGAHMMWGFFPLYWHLLDYVPSATLTAYRVIWSFLLLMTLSIAMPQLRRALLQLREPRKLAIYAATATMIGINWGAFMYAVGSGQVLQASLGYYINPLLNVLLGVVVLGERLKPFQWIAVGFAAIGVAVMVMMGSGMPWIALAMASAFAIYGLLKKKATLPPLEGLSIETGLLFPAALAFLLLQSPDPGAQPYSPVTWLLLIIGGALTIAPLALFATAAKRVTLTTIGILQYVGPTLQWFVGVVLLGEAFGGSKLIGFLFVWTGVTVFIVGGLQMQSRATRQARQVALAE
>NZ_CP036292.1|WP_145117465.1|567645_568386_-|methyltransferase-domain-containing-protein
MTHRSFLHISLAALFALSVQTSARLEAQQTATEAPATIPLPAGINDNFKDPELNVSEWLDRFEVESREVYAGRKAVLEACAIKPGERIADVGAGTGFYSQLFAKTTGWDGWVYSVDIAPSFLQHIASRATADGIENLTPVLGTDVSIRLPSESVDLVFICDTYHHFEKPMQSLASIYRALKPGGRLILIDFDRIPGKSREFILGHVRAGKEVFQSEVIAAGFQFTDEVEVDAFEENYLLRFTKPRK
>NZ_CP036292.1|WP_145117466.1|568541_569624_-|hypothetical-protein
MSSSTESATPNSPDDLDNANGESARRLPKKKTRAEKLGRSTVMLLRRIHLYSGIFMFPWVLMYGFSGWMFNHPRMFTADEVTTYHAADLDAGLLTDLTSAQQTAIAVVEQINLLTSESQGPELRITDDRRPLFSGHLEYNVNTPTAKHQLAVNPVTGDGEVRTTLVDAEADDAADDKSDPLAEVYRVEIEPNVSADIQRQIPEVLDQLGLPSNRASLGYRKLSVVFSAEADGIPCIVSYNLADGSVNSVREDDRPQLTKKAFLQRMHLGRIYTPVVEIRWLWALLVDVMFVSMVFWGCSGLLMWWQIKRTRWLGMGLLATSILFATFVGLGMHDQMTSTGPPKKIPAEKATDTKASNQSN
>NZ_CP036292.1|WP_145117467.1|569951_570752_-|hypothetical-protein
MRLLIDGYNLLHQSDLMGTGHGAAWLERARQRLIDTIAAYLEPQDLPQTTIVFDRHSGKQIDAHQVDSSGIQIFYAVDHPEADDLIEDLIAKSSHPKQLTVVSSDHRLQKAIDRRGGKSVDADIWYERLLAGQVTTGAKKNKQGRGNRQAKRGKSHKPDSPLTDEQLARWLDRFNADAIQDELSSLAEEPSPIPKPCPPALPQPKAKPAKKATKQKSQPKPLKKPAPPRSKKKQPATKPDDLSKRKLQQENYNPFPEGYTDDLWDE
>NZ_CP036292.1|WP_145117468.1|571010_572564_-|2-isopropylmalate-synthase
MPVNDNESTETRHIKIFDTTLRDGEQSPGASMNLNEKLEVAQMLVELGVDVIEAGFPIASPGDFEAVREIAQTVRGATICGLARCAEKDIDRAWEALKGAPQPRIHVFLATSAIHRQFKLKMTTDEIVERAIAGVTRAANVCDDVEFSPEDAARTEPDFLCRVVEAAITAGATTINIPDTVGYTTPTEFHARIKMLIDRVPNIDKAVISVHCHDDLGMAVANSLAGVQAGAGQVECTINGIGERAGNCSLEEVVMALRTRSDFYKVDTRINTQRLVPASRLVSSTTGMSVQRNKAIVGRNAFAHESGIHQDGMLKEPTTYEIIRPEDVGFAKTDLVLGKHSGRAALADRARQLGFQLTGEQLQVVFERFKALADKKKEIYDGDITALIQQQISGNNQAQWSLVDYEVRNSRTSTPTVKLTLRRGDEEHSAEVNQGDGPIDAAFWAVEQITGMKVMCKDFQVHSATLGRDAQGETTLEIEYNGKTYRGIGVSTDTVEATILAMLNAVNRIAAETENAS

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Crispr_ID: NZ_CP036292_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_5

670450-670581

Orphan

Consensus_repeat	Method
CCTGGGGCTTTCGCCGCCAGGCTTTATGCGATCGCCACTCCGCGGCTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_5

>merge|NZ_CP036292|5|670450-670581|CRISPRCasFinder
CCTGGGGCTTTCGCCGCCAGGCTTTATGCGATCGCCACTCCGCGGCTGGGTGCTGGTAGGGCGTCGGGGGGCAATCTTTGGAGGCCTGGGGCTTTCGCCGCCAGGCTTTATGCGATCGCCGCTCCGCGGCTG

>NZ_CP036292|5|5|670450-670581|CRISPRCasFinder
CCTGGGGCTTTCGCCGCCAGGCTTTATGCGATCGCCACTCCGCGGCTG	GGTGCTGGTAGGGCGTCGGGGGGCAATCTTTGGAGG
CCTGGGGCTTTCGCCGCCAGGCTTTATGCGATCGCCGCTCCGCGGCTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145117536.1\|682141_698104_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366080
NZ_CP036292.1\|WP_145117535.1\|679360_681937_-\|carboxypeptidase-regulatory-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|366080
NZ_CP036292.1\|WP_145117531.1\|670621_671437_-\|histidinol-phosphatase	unknown	unknown	gnl\|CDD\|238819
NZ_CP036292.1\|WP_145117528.1\|666934_667393_-\|carboxypeptidase-regulatory-like-domain-containing-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123973.1\|659997_660651_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117522.1\|659022_659571_+\|YqgE/AlgH-family-protein	unknown	unknown	gnl\|CDD\|234694
NZ_CP036292.1\|WP_145117523.1\|659634_659994_+\|cold-shock-domain-containing-protein	unknown	unknown	gnl\|CDD\|239905
NZ_CP036292.1\|WP_145117537.1\|698595_699339_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145117524.1\|660829_663511_-\|carbohydrate-binding-protein	unknown	unknown	gnl\|CDD\|369642
NZ_CP036292.1\|WP_145117525.1\|663671_664667_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145117530.1\|668870_670295_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP036292.1\|WP_145117533.1\|672346_673771_+\|threonine-synthase	unknown	unknown	gnl\|CDD\|235757
NZ_CP036292.1\|WP_145117539.1\|700997_701480_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117529.1\|667611_668901_+\|VCBS-repeat-containing-protein	unknown	unknown	gnl\|CDD\|379232
NZ_CP036292.1\|WP_145117527.1\|665778_666786_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145117532.1\|671414_672116_-\|signal-peptidase-II	unknown	unknown	gnl\|CDD\|376504
NZ_CP036292.1\|WP_145123974.1\|673936_674362_+\|YraN-family-protein	unknown	unknown	gnl\|CDD\|237119
NZ_CP036292.1\|WP_145117534.1\|674406_679071_-\|tandem-95-repeat-protein	unknown	unknown	gnl\|CDD\|333740
NZ_CP036292.1\|WP_145117526.1\|664770_665106_-\|carboxypeptidase-regulatory-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|379297
NZ_CP036292.1\|WP_145117538.1\|699670_700858_-\|lipid-A-disaccharide-synthase	unknown	unknown	gnl\|CDD\|234580

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145117536.1\|682141_698104_-\|hypothetical-protein	gnl\|CDD\|366080	pfam00404, Dockerin_1, Dockerin type I repeat. The dockerin repeat is the binding partner of the cohesin domain pfam00963. The cohesin-dockerin interaction is the crucial interaction for complex formation in the cellulosome. The dockerin repeats, each bearing homology to the EF-hand calcium-binding loop bind calcium.	7.0967e-07
NZ_CP036292.1\|WP_145117535.1\|679360_681937_-\|carboxypeptidase-regulatory-like-domain-containing-protein	gnl\|CDD\|366080	pfam00404, Dockerin_1, Dockerin type I repeat. The dockerin repeat is the binding partner of the cohesin domain pfam00963. The cohesin-dockerin interaction is the crucial interaction for complex formation in the cellulosome. The dockerin repeats, each bearing homology to the EF-hand calcium-binding loop bind calcium.	1.40666e-07
NZ_CP036292.1\|WP_145117531.1\|670621_671437_-\|histidinol-phosphatase	gnl\|CDD\|238819	cd01641, Bacterial_IMPase_like_1, Predominantly bacterial family of Mg++ dependend phosphatases, related to inositol monophosphatases. These enzymes may dephosphorylate fructose-1,6-bisphosphate, inositol monophospate, 3'-phosphoadenosine-5'-phosphate, or similar substrates.	1.6353e-86
NZ_CP036292.1\|WP_145117523.1\|659634_659994_+\|cold-shock-domain-containing-protein	gnl\|CDD\|239905	cd04458, CSP_CDS, Cold-Shock Protein (CSP) contains an S1-like cold-shock domain (CSD) that is found in eukaryotes, prokaryotes, and archaea. CSP's include the major cold-shock proteins CspA and CspB in bacteria and the eukaryotic gene regulatory factor Y-box protein. CSP expression is up-regulated by an abrupt drop in growth temperature. CSP's are also expressed under normal condition at lower level. The function of cold-shock proteins is not fully understood. They preferentially bind poly-pyrimidine region of single-stranded RNA and DNA. CSP's are thought to bind mRNA and regulate ribosomal translation, mRNA degradation, and the rate of transcription termination. The human Y-box protein, which contains a CSD, regulates transcription and translation of genes that contain the Y-box sequence in their promoters. This specific ssDNA-binding properties of CSD are required for the binding of Y-box protein to the promoter's Y-box sequence, thereby regulating transcription.	7.18638e-10
NZ_CP036292.1\|WP_145123974.1\|673936_674362_+\|YraN-family-protein	gnl\|CDD\|237119	PRK12497, PRK12497, YraN family protein.	2.83893e-35
NZ_CP036292.1\|WP_145117522.1\|659022_659571_+\|YqgE/AlgH-family-protein	gnl\|CDD\|234694	PRK00228, PRK00228, YqgE/AlgH family protein.	3.07389e-18
NZ_CP036292.1\|WP_145117538.1\|699670_700858_-\|lipid-A-disaccharide-synthase	gnl\|CDD\|234580	PRK00025, lpxB, lipid-A-disaccharide synthase; Reviewed.	3.66116e-103
NZ_CP036292.1\|WP_145117537.1\|698595_699339_+\|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.	2.72436e-12
NZ_CP036292.1\|WP_145117525.1\|663671_664667_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	2.72984e-60
NZ_CP036292.1\|WP_145117530.1\|668870_670295_+\|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.	9.56648e-10
NZ_CP036292.1\|WP_145117533.1\|672346_673771_+\|threonine-synthase	gnl\|CDD\|235757	PRK06260, PRK06260, threonine synthase; Validated.	2.96086e-141
NZ_CP036292.1\|WP_145117524.1\|660829_663511_-\|carbohydrate-binding-protein	gnl\|CDD\|369642	pfam07995, GSDH, Glucose / Sorbosone dehydrogenase. Members of this family are glucose/sorbosone dehydrogenases that possess a beta-propeller fold.	5.56047e-34
NZ_CP036292.1\|WP_145117527.1\|665778_666786_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	4.71645e-62
NZ_CP036292.1\|WP_145117532.1\|671414_672116_-\|signal-peptidase-II	gnl\|CDD\|376504	pfam01252, Peptidase_A8, Signal peptidase (SPase) II.	6.08111e-29
NZ_CP036292.1\|WP_145117529.1\|667611_668901_+\|VCBS-repeat-containing-protein	gnl\|CDD\|379232	pfam13517, VCBS, Repeat domain in Vibrio, Colwellia, Bradyrhizobium and Shewanella. This domain of about 100 residues is found in multiple (up to 35) copies in long proteins from several species of Vibrio, Colwellia, Bradyrhizobium, and Shewanella (hence the name VCBS) and in smaller copy numbers in proteins from several other bacteria. The large protein size and repeat copy numbers, species distribution, and suggested activities of several member proteins suggests a role for this domain in adhesion (TIGR).	1.72589e-07
NZ_CP036292.1\|WP_145117534.1\|674406_679071_-\|tandem-95-repeat-protein	gnl\|CDD\|333740	NF012211, tand_rpt_95, tandem-95 repeat protein. This 95-amino acid repeat occurs in tandem in proteins that may be several thousand amino acids long.	1.00739e-16
NZ_CP036292.1\|WP_145117526.1\|664770_665106_-\|carboxypeptidase-regulatory-like-domain-containing-protein	gnl\|CDD\|379297	pfam13620, CarboxypepD_reg, Carboxypeptidase regulatory-like domain.	0.000445629

>NZ_CP036292.1|WP_145117530.1|668870_670295_+|tetratricopeptide-repeat-protein
MDQSRRGKTMKRLKQLLIVILVLEVIFCGIYVKRRLWNHHVVLPAVTLDDPLLAAEFQQLADQATAGGSAEWQALGEGLLGQGFYGEAEHAFRAAVDIDPSNYLAHFALAFCLDRTGRIAESSEEYLKAAEIQRKSKQLVGSVEHCLYQVGKNHLREEDAAAAIDSFASQAGFAPASYQYAKLLVRDGKVDRAMPVLKMELDKTPLSLKFNALRLQALESTGQQRLADEAADVLQRSQYQIPIDLNTDYVTPMNQRLGISRQLQEYNELLASGDMDLLAKHLQSMWDVVEPTTLNQKSKILISMAEVAFQRRRAEEMLHAVDRLKELGVSSPDMLQLEGAAYQLNGDIDRAIALWIRASEMSPNIPLHQILADAYQQKNDDARRDYHRGQAALLEAKLAYWNNQWEPAKQAAQRAIDVDPSLDQAWFYLAEIERELGNPQPALEAYQKCLDLNPNHGRALAAESRLGEKAVDSE
>NZ_CP036292.1|WP_145117529.1|667611_668901_+|VCBS-repeat-containing-protein
MSQIAVLLLLILAVPLVAVYVPSVVGSLSPLPVVFQGGTTCPASSVQFDQVALGGTSVGLPQITNVQVLDFDGDGANEVLACDSLKNQVVLFRQVDGEWQEEVLVPDVAAPAHATAVDIDSDGDLDLVVSVLGNILPDDSVIGRVELFEATPDGYRRHVILDDVRRVADVQPADFDGDGDIDLAVAVFGYSRGSVLWLENRGELKFRDHLLHTAPGTIHVPIADYDGDGDLDIAAIVTQDEEELWGFENLGQGEFKKRRLWMTINHDLGSAGLVQADLDGDGDPDLILPAGDNLEDLDAYPQPYHGCYWFENQGDWTFQIHRISDLGGTYAADVGDFDSDGDLDVVLASMTNNWNRTDTASLVWLENDGQQNFTTWQIASDPIHLVTVAAGDLDGDGSDDIVAGALNLRKPFQRVSRVSAWINQGEGKQ
>NZ_CP036292.1|WP_145117528.1|666934_667393_-|carboxypeptidase-regulatory-like-domain-containing-protein
MTDPRRFVDSTNTKINSTLVTKFVAIVLLLASVGCVGSGLVMPETGEVEGIVTLDGQPLPNVSIVFQPQENPQARASMAVSDEQGRYTLTYHTDKQGALIGMHTVSITTPTDAPDPSGQSKDPIPARYNSQSELVVEVKAGSNDIPLELTSK
>NZ_CP036292.1|WP_145117527.1|665778_666786_-|DUF1559-domain-containing-protein
MSQHPQRHSRRGFTLVELLVVIAIIGILVGLLLPAVQSAREAARRMQCSNNMKQLGLALHNYHDTYQVFPSGCIDSNRKTNSPTDALNNNNGLGWGTLLLPFIEQSPLYDQISFETGSFGRSWQDKNNDGTTNDPIDSAKVVIDAFVCPSDPMSGLNSDKSDYGKSNYMAIAGRYAVQTDSNGSPLGQRNGMFFENSNRKFRDVIDGTSNTLFLSERTTQNDNVNSTQCGGAPCNWAGGLWIGPRIVSSSAAWHTGLYLFDVANVGGYDTGYSLTHGFGRSSATWGADWNAKGCHPGGMQATLGDGSVRFITETIDFDLYRNLHTPQDGNVISNF
>NZ_CP036292.1|WP_145117526.1|664770_665106_-|carboxypeptidase-regulatory-like-domain-containing-protein
MPETGLVEGTVTMDGQPLPNVSIVFQPQDDPKARASMALSDEQGHYSLSYHADKQGALIGPHKVSVTTPSDAPDPSGQAKEPIPAKYNSKSELVVEVQAGSNDIPLELTSK
>NZ_CP036292.1|WP_145117525.1|663671_664667_-|DUF1559-domain-containing-protein
MIQRNHRSSRGGFTLVELLVVIAIIGILVGLLLPAVQAAREAARRMQCGNNLKQIGLAMHNYHDTFQVFPSGCYDSNPATNSPGDAANNNNGLGWATSLLPYIEQSALYDLIGTETGGFARSWQDKNGDGSANDPIDSASVVIDAYVCPSDPMSGINSDKSNLGKSNYLAIAGRSAIQTNSSGNPLGTKNGMFFENSNRRFRDVTDGTSNTMFVSERTTQDDRIGSLQCGGTDCNWAGGIWIGPRIISATETWHTGLRMLDVTNVGGESLTYGLGRTTASWADDWSAKGCHPGGMQVTLGDGSVRFMTETIDLITYRDLHTPQDGNVIAPY
>NZ_CP036292.1|WP_145117524.1|660829_663511_-|carbohydrate-binding-protein
MPNSPRSFAPLCLSLLLCCGIIPATPLHAEEVDVERFERTTVYSELTQPMELEIAPDGSIFLIEIAGLVKRIDPQTGQATVVGKLEVTTAQENGLIGMALDPNFTENGWIYLQYSPPEFSGQHISRFDFRDGQIDLASEKLMFKYEEQRRECCHHAGSMEFGPDGNLFIGTGDNTNPFKDSQGFAPIDQRENREPWDAQRSAGNTKSYNGKVLRIRPEPDGSYSIPDGNLFPKDGSIGHPEIYVMGCRNPWRISVDQKTGYLYWGDVGPDAGSDNDRGPRGYDEVNQARAAGNFGWPYFIGNNFAYPMVDFASGEIHPAQDPLKPINESVNNTGSKELPPAQPAMIYYPAAPSPEFPEVASGGRTACAGPVYHYDAQSKSTTKFPAAYDGTLFAFEWSRHWIMAVHMDKDSNVQRLEPFLPEMKFARPIDLQFDAAGALYVIEYGETWGVNPDARLVRIDYVRGNRSPVAVASAESTVGREPLIVKLSAADSYDKDGDSLTYQWTSVRSGVTPPVRKPIATTAVAEASFAEPGVYTIELTVTDPSGATNSMSLPVIVGNARPEVKFLEPQNGDFFSPGKPIRYRLQVRDIEDGTSDFDEAEEEGWHLIEGLAPTRLFVEASAVADEGAAANVPPGLALIRKSDCLNCHAANRRLVGPSFVEIATKYRDQPHEIEKSVARVRQGSTGVWGKIGMLPHQQHTEAEVLQMVQYVYAATADSSAPTAQGFNNELLAIETPGKMRLEATYTDLGRDEIPKLIGTAEVVLRSRNMQAESADEISGARELGSGKAEGKKFIGAINHDAFLKFNDIPLDAIASIAVRVTSAGAGGMIEVRRGTVDGPLLGSVLVEVNGSWDAFEEKQIAIDPSSGRDALFIVFKNEKQRGGLMNIDSLRLE
>NZ_CP036292.1|WP_145123973.1|659997_660651_-|hypothetical-protein
MKLAYTAFTAVLTVYYWREYGPTNFLYFCDIALFLAVLAVWTEKPIYASMAAVGITIPQLLWQIDFLGAFAGVRVTGMTEYMFDDSISLIARGLSFFHFWLPILLLYLVWRLGYDRRALIGWTIIAWGAMLIAYFALPGPGDPLAFPNQPHNVNYVFGPDPETAQTWMPGWAWLSCLMLGLPALFYLPTHAALAYWDKQTRRVDVAPESGNRMPSAI
>NZ_CP036292.1|WP_145117523.1|659634_659994_+|cold-shock-domain-containing-protein
MNIRYDDEYIQRKRVGEIRNIDPVKNFGFISGEDFRGDVFFHMSVWESDRNMLPEIGMIVEFEINQVHLQETDSLRATVVRRTDRPYTKQLDLKADESLTVKHHPNARKRKPVWRGKKT
>NZ_CP036292.1|WP_145117522.1|659022_659571_+|YqgE/AlgH-family-protein
MEQSIVGNLLVAAPALDGTLFQRSVCLLLHHDQENVIGVVLNRPLFGGISLPQGNSPALLVKQSLHLGGPNAGPVFALHNCADLAELETGTGLYMASSRQHMQRLLADASLPCRLIVGHVQWSIKDLQSQLSSDLWRVLPATPEAVFEPDDLMWSDLARKSAALHFAHLVGAKHIPSHPALN
>NZ_CP036292.1|WP_145117531.1|670621_671437_-|histidinol-phosphatase
MTTTPPSEWSARDEGRVAAMIDLAHAAGQLTLNFFGDATLAVDRKGDASPVTEADRSAERLIRQRVAESYGDDAILGEEFADTQGSSGYRWIVDPIDGTKSFICGVPLYSTIVAVEKDDQVIAGAIVIPALGESIVAAIGSGAWHRRNSDADWTAAHVSPCDRIEDAVFLTSQVDSFANRGAAAAYDSLQSAASITRSWGDAYGYLLVATGRADIMVDPIVNPYDVAAVQPVLTEAGGQFSDWKGNPTIRGGDAFGTNGKLHAQVLSHLGG
>NZ_CP036292.1|WP_145117532.1|671414_672116_-|signal-peptidase-II
MLSPNGDPQVLANAPADRSNPPPQSRDGSPLPHSNPLPAIPTNRYITFFALAILGAVADLWTKQAMFAWRGLPGMRPPHWVVEGYVGIETAVNIGAVFGIGAGKGQLFAAISVVAAIAIFVWLFVKRAAHQWLLTIALGCVMGGIIGNLYDRLGLWWEPGMDPRWQSGVRDWILFQASDTLKWPNFNIADSLLVCGAAMLIYRSFFPVDEFDDDKPNSQEDSNEAHRDNNSSQ
>NZ_CP036292.1|WP_145117533.1|672346_673771_+|threonine-synthase
MLQTKPSHRKTEGIALQKCISPSCGATYEAESVRTSCDRCGDLVDVIYDWDRGTVPAKLKDFEQFWTQRHDRLRFSGVWRFKELLPFAPDDKIVTVGEGQTLLQQAESVAQYVGMNAGQLYLQYEGMNPSGSFKDNGMCAAFTHAHMMGAKRAACASTGNTSASLAMYCAVSQLMKAIIFVGSGKIAYGKLSQALEYGALTVQIAGDFDDAMIRVKQVSDELGIYLVNSVNPFRLEGQKTIMFRVLEALQWEVPDWIVVPGGNLGNSSAFGKAFTELKELGLIDRIPRLAVINASGADTLYELYERRGVRWNGGNVDMDPIRAFYDEMDRDGAKADTIASAIEINRPVNLKKCLRALEACDGVVRQVSDQEILDAKAKVGAGGIGCEPASAASVAGAKMLRREGVIAPSDRVVCILTGHQLKDPTATVAYHTTDQAVFNDVLGSRGVQRASFANRAVALPNDLEEIIKAIRLYS
>NZ_CP036292.1|WP_145123974.1|673936_674362_+|YraN-family-protein
MRRFDDWRFGKIDLSRPLGERGEQAAERYLRKLGYRIVSQNDRQGIGEIDLVAVDKRTVVFVEVKTRTSDHRGHPADRIDADKERRLTRAALSFLKRHRLLEHRARIDVIAVWWPPGLEQPERIEHYQNAVEPTGQYQWFS
>NZ_CP036292.1|WP_145117534.1|674406_679071_-|tandem-95-repeat-protein
MAMNQLRQRFLKSRKKNSSRQRRKLFGEALEGRRLLAADIAVPMDGLNPHHNYIFGTDTNRDYQTTAVDALIVINRLNSASASASGELGSTNEDGVFPDVNNDGLITPIDALNIINTINRGEGELAAVLKLSLDVSQDNQSLLRDTGASTTANPMTTRDFELEVGEKFNLEVRWTHFGNDPFSKPLGAFTVYADILANNKDVFAPVLSETQILTISENLVDARSGNFELSFPGGDTATVSLADVAANGFENALASGIEEAGNFESGSISVFPSGVRSTREQNEETGVGDPYQFVVRYNGDNEEFQNIPALNVVANFSDAGGQALTIDATTAEIPVYLNNNQADGLNPDAFRYNIDFRSSNLNESALYTSSPSGNYTLTGDGNPDGDDVIFDEVGGFSNNISPGGLPTIVPNPNQYNGQDFEAYSLELVVVQPGDVTFSLNMPDLVGNQLTVFGSDEALTEDGLVEIDLSENGEGLVRGTFVAPPQDITIGADSITAVEDTARTFDPVANDTEINGGTLTLKSTDGFTQPTNGTVTRDGSTNTLTYTPDANYNGPDSFTYTVVNSEGVEATGVVSITVSAVNDPPTAVNDSGTGLTTPETDSLTITAARLLANDLKGPANESSQTLTVTGVSSTSSKGASVSFNSSTSEILYTPLSGELGNDTFTYTISDGAGGTATGTVTVNVTDVNTPPVAVNDTIAVTEDVPLTIDVSDLLANDSDDNNILSIASVTAGSGASAGSVVLNSGAGTITYTPAANVFGSNADSFTYTLTDGVNPGVTATVRVNITGVNDAPVATDDALTVDEGLTPRTLDVLDNDNAGPGEGTSVTITDVTALPAGAGTIAIAGDGQSLIYTAPSANYVNTAIDFSYTIQDSEGLSATADVTLSVVPTVRPRAIPDVVNINEDSGAIDINVLSNDLGNVGESVTLESIDTTGFPAAAGTLAIDDNGTATKTDDVVTFTPAEDYFSTSGLTFTYTISDTSGDDSAAAAIGANTATVTINVASVNDKPVFGADGLFQIDEDETFTLPASVLANDSAGPANEQQTLAISAVAATSAAGGTVTLDGGVVTFQPAADYHGNDSFTYTISDGVDTTTATASFSIASINDAPNLQPVTQLTQGSEAITLDRSTLLSGATPGPADESSQTLTIFAVSNGGTTSGGGTVVLNADQSVTYTPVAGFSGTDTFEISVRDNGSPSEFSIATVSITNNAAPVVGNDTVSTYKGLTKTILVSDLLANDSDAEGDTLTITSITQPSVGSATLSADGTTITLTTPSETSAEETSFTYTVTDSFSDRVGTVAVEILPFQPSTISGSVYVDQANGSEPNGSQDEGEVGLGAVWVTLTQEGSAPQSVLSDAYGNFVFENVAPGDYTLSYAPPSGVVDSASNPNSISLSIAPAGGETYADISFTADSFNATAGNTLDRYIGSYLMALQRANPSMTTADLDALAQQGIVFGLNTSGDMTFMYVKGGSGFDSTAAISATLSEDGNQLELTKLYADGRVSDPVIIQRALFISVADPDTGDTVIRVLGNVNFVPSITAEGEADFSDYTQAVDQIFGGL
>NZ_CP036292.1|WP_145117535.1|679360_681937_-|carboxypeptidase-regulatory-like-domain-containing-protein
MSHPLRLSRRRNSRNRCALQVEHLESRQLLAGLPLGATAADTGEYFLGRVAVTPVLIESDGSIDTSTQDWSETEIAATLAKVTEGVQWWADTLDQLDTVHSLEFVIDDSFATTPYESPFEPIDRPSDDYQVWISQFLRDVGHADVDSLEQGIREFNDAQRQKLDTDWSFTIFVAASDPNGQFAPGGSFSTAFALPGGLFFVSPASRPASTFAHETGHIFYALDEYAGGASAYRTRGYYDSQNLNAINNNPDPGFVQEPSIMSGGTSLQTAYVNHTSSAATLALVGWQDSDGDGIFDVLDVPLTLSGSGRFDSTTGTYRFQGSAAAQALPNQNSTGLQNDITLNEISRIEYRIDAGDWLIASQPNAQTATLDLRIAIDVPFNLIEIRAIDQQTGITSNLFTGSSDLPATTESSAAIAGHVWLDRQNDSEFDAADPGVADVSIQIVDQLGQPVSLIQGVEPDDYPAAAIPATPGVTLSAVGTSISETISASVSQFATTGEQVFAAFNTAQFRNSESWSSARDQIFQATFDEPVASVWIDATALASPSYARIEAYDASGELIHRITSDAIAVETSTTLQISTATRQIASIRAYGHAETSIALDNLRFGTETATSTDNLGTFSLNGLPDGQYRLEIESDRPEIYQVETPLIDIEVVDGVAQAFAAVRVTQLTSPWQNPTDRYDVNASNSIEPLDALQILNEINRSGSRQLTASDIGSRYYDVNGDGMIAPIDVLQILNELQRNPADAGEWYADAGSEPQTGSQTDGDSASAPFAAAVSARFQTADAATQVAEGEHEQATDKFFAALSSASFAGTMGQHPKAGQPVAPLNLEQFASPEETDEPKNSLESESGPLEPLIQPLQK
>NZ_CP036292.1|WP_145117536.1|682141_698104_-|hypothetical-protein
MAIRKTGSSVNDSSNKSRRSDRAAKRQRLNSRRSLLETLEGRQMLDAGPMLVGVQPDTEPLLQDMAELNTSPREITLRFDELASLDPNSLDGIKIIRAGSDGEFASASAVTDLGSSGAVELTFEAVQSGSAGDNLEIVFTKVSRTDKTLPIVTVAGQRIQIELNSNPALVTRASDIQYGIAQNPDAAALLRVASVSGQTFFDVGRTAQQGQTLTLKGSDRAQATSQLGAANTQVRFTAVASGVAGQDLAIDVRQSFRVAGAPPIVSVIGDRIEVLINSNPASRTTVGQLVTAINAHPQASLLVSAELETGSASSTIGLDLSAFSPIEFSLQNGDLDIEVVPGYVGFVDASQREVVFRFADDLPQDRYRIQIDGTSANALQNTQGDKFNNGVDQTIEFTINSAPTIQAIVPQPIVNGQQLRDQVWVYFDLNDPLDASTVRNTALYQLISTGGTETGADDVTRTPVSVNYNPGTGVAVLQFSGDLYSLFPGTDVKQFRLRVGETDVRGTDPTVLPAVVEPGDSFALARDIRNDWIVSPNNISSVVIEGAIAKTEFINGVPVSNNEYLIDFPGGAGAPGVQEFRPEDPSSYGAPQADALDGISTYFYNFFGQYRGDDPTTATVDDDRVLFNNITEQQKQRVREVLDLYSQYLGVQFVESADMGLQIAVGETLNTSVSWEVSDDLGVINSRLVDESDDDLFGQQFFELATGMVKDLIGVSDFLSPLDASADPLYPSPRDIIEGQYSYRPDSTDIDIYKFSVPTSGEVTIETFAERLAGSASLLDTNLRLYRELSNGTIEEWAGNDDYWSEDSEITVDLPAGTYYIGVSASGNDSYDPMIEDSGLGGLSEGAYELRMSFKPSSATTITDTTGIALDGDNDGIAGGAFDFWFESASFTDTVFVKKDGGTITPMVNNAISGTAKGAVTTISTALSGATSQGTEIIRILPSGDGNLATTADNQPYLIGFDDFGRELADGSSFQVPQDVTVMIDSGSILKLRRARIGVGSSSPVVDFSGGSLQVLGTPLFVGANGSQATVTPVSGDVVFTSLADTSIGGTQSGNVASPGDWGGIDFRSDVDKVDESRIDYEAEGIFLNHVQYGDFRYGGGTILVEAKPEVISPIELSGTRATIANSTFTSNADAAIEASANTFEDDKFTLFEGQATPDYTRVGPSVYNVLFEDNSINGMFIRSQTRDGNGVEKLSVQARFDDLDVVHVIAENLEIQGTPGGAIVESTAPPTRIVRLTATAGGTLPVGEYSYRLSYVTQNGNESPVSNATGTVTTTAANGTIQLEQLPAVPAGSDFVARRLYRSVDGGSYQLVATLNGSSTEFRDTGLAAGAAIDVNRPNVDDVELTATAGGELPAGEYEYKVSYVDANGNELAVSFATEAISVPGIDIDDNTIQLSNLPTSANPSVVARRVYRSFNGDAFRMIALISDNTSTQFTDAGLVSGMTLIENLRPRMDARLAIDPGVIVKLSGAVIEVEQGAQLLAEGTAGQQIVFTSLDDQRFGRGGTFSTNQANANTVFQAGDWGGIYVGPGAQASLDHVRVTGAGGGARIDGKLSFFNPIEVHQGDLRLTNSRVEESGTGFAAGDSDRTGMQTHEAAVIFVRGAQPTIASNTFINNDAVAMNFDLNSLDNTYVSDPGTSIGRLEKVQGTSLGNQGPLVFDNVLENNAINGMEVRGGELATAGVWDDTDIVHVVRGTISIPNHEVYGSLRLESAPDRSLVVKFQSEQSPATIIAGGDASGSAEQFNGLADRIGGALQVIGQPGKSVILTSLSDDTVGSGFDTQGKPQTDTNNSRNDEIGSTTLLLPTGPEIPRGTIIDNDVANDVAGHFSFQPEAGGGVGATVGGGFNEVTTQGANTFFQQQDALFDYLNFIDVGADGAAVELGTTTITTPTTFLSDDVVYSEGTFTGENGLINWRVEQSFEDGSPTLITKLTLSSPTPLGDLRFINYYDPVIASDAGDLLFTEGTPGTNDYRVTVLDGPERVGFRHYGTFEQGTGLEGANYEGWIADEFPDLITDPVFNLPFTPTGTIDTASVPLANVTDLPAPVYGPAITTTAHAWLVNPTATTVTITSALELIEDVFDDTVGLGKPGDWDGIVLREAAHDRNVEAAVEQEGDLSVNRNDQIALAQYLGELAPSTSAGSENRRIGFQVYGNIDQPSDVDVYSFDAEAGTEVWLEIDRTNSSLDSVIELVRVMSSGDDADNDGISDSIVAISNGSISEAIDSGLIIRDENAGSLERTVSSGQVNSLNNSMFTASANSAFNTPQDLYSTNPNDPGLRVVLPGETGEVFTYQVRVRSSNLQLNDPVSKLFSPVTGAKIDEGKYDGLTSGPYELSIRLAESDETAGSYLNLADIRYATTGVSVIGQPFNSPLLGDAVEFIDQAGSDNNDTLATAQQLGPYGTQGDPNSNDSLSIAGAISSDTDIDWFQFSIADSASESSLRNYVSTVFDLDYADGLGRGDFSLWVFDQNGQLILTGLDSNVADDQPGNPNSSDFTSLSRGSTGTADPFIGAVELSAQGDATSNSQTYYVAISGLNNMPSVLDQFTTAAATNPLVRLEPIESLIRIAEDHVSFVGGSTYAPTTLQSLLFDPITAASPLTLNDMKLYVSTSGSADNLRLVNAYTGQNYGTIGTTGGQIFNDIALRANGDLFGYNINGIVDDASWHYFNIDTGFGNVTDLTPTGTNLTTHETLATVDANGNVTRTIVQTDSGVTVNAITFDAVNGAERGFIVGDRGPGNEVIWTNNILWEINPSTGNINGVGLPANPPAAGFAGAYTDPRERGYIETGNPNNLPSTRLGVTAASVVDANGFLAPSLTDGLTFTIRDFVNAGSVLFQFDLGSAIQLSSNVRGGTFLRDGETITVGGQLFEFDTGIRLDVVGSEDPLAGGVAEGSRVTLTSKSTGMAYTFEFDSDGRDFTGRDFSRPDLFAVNLDASTTDASAATILASAINAADIGIRATASNTGEIVLTGATGAATTIGLGVSSLGADGITTANATAIVVDEDLSATDLTRAVSDVLRANQVAIATAGTRIDFTDNPIIDLDLDTPLGVGQAISIVGTANTTGGPTVIPFDVDDTAADIGARVVDAIQAAVDSGLLTSVTATVDGNTVAFSGANVLTAAGALDVAGIAPGGQVTGIAVPTSGDMYAVSNAGGLYRIDSGVISPVRVNFTQNIGDYVDTATDLLGINFTGLSAGPENLAGGAYSDLLFGITGNGDIYAFNTRGELQPIFANGASRISTGVAGATGFDFGNLDYNLWHVTSDTFAGSTTPITLPGHGINATFNDTRTATAGGTSWYFGLDDTISTGTLNARTTRVDGTTVNGTYDFAGGAHGELVSNAFSLEGYNSADLPTFYFNYFLETDSDGDRQLEDSLRVYLVDEDGSEFLLSTNSDSATASTVNPNLSVSDVLTLDQAQETFDNTGTWRQARIALDDFAGQKDLKLRFEFSTSGSMEFGQSELQAVTGEEILDGDRFQISGRDYEFVLSPLLTIPAGNQIANGELIAIDDVVYQFTTDASTVLSPNVAVVYDPTQSGEEIAQSLHDAIANYTTVTNTDYDTDQDASQQNDNMSTANILQVPGGQTTINANGSIGTPNGSQQTVDVDMMRMELSAGQTIMLTVTESTLAPALNPIARVFNAQGVELARELSVDGNTVVSFEAPADGTYYIGISGEGNGNYDPTDNLGGRTFGKSGAYSLELVSTRPYDIRVAGDQVILNGTGPALFSANSTIDVVGNDGSSGIPVNINRDMTATEVASAIADAIRDTLGAGQIITQQGGVLSLPGLRINNAGPLNIPVRTGDAFGSPTVEMARDNDHRGVYLDDFIIGFRERGEFVTSAGNTNDFVPNSGFDLNGDDVASTQTGEYQLEIRGASEYVLSQSLPNPVSMFRSFDTNDRLVQGVTLETLSAEELDAAATALADLILLRNNDPTLEDIDPDTRLSFTLSDGQTSITFEFVNEASAIEPLEGSVPIYYSTGVVNPISGESVSETAADIAAKITDAINLPDVQALLDISALSSSGETSATAAAAGDSRINLSGNVNIIENLSGLSSQILGDSRKPGTDELPTVELFAQSTQALALDRRGDSNTGSEEQGVIKIEGVAVSYSSQFGIDLDHGADVGKFMYPKNLVELNSYVDANGVVHAGLAPGVVVQSNLLAYNRSGGINVQGIDTSNGSQRSMVAFDRIVNNTIIGGTISPTESPGPATYDGTTYANGSISFADVVVSYDPSTTTPPALGLQISAEILGVPDYTGGVAEPTPNAGQGAVSLGGGGSITVQFVDNRLVGSGDASPDLEIFEVGNAEPVLVEVSVDGITYTSVGTSVGGANQIDIDRYGFGPNDRISFVRITDQNFGSALDQAVGADIDAVGAITSVPADQFEAGGVGIALSNGVSPTLLNNVFVNNETAIDASGNVVPNHPVVLGANTFQANTVALNDPNSALLDNVLARFVDPFTNLFVSASDSIFIPAQGSDLIDSSINSLADRPQLQIVRETVGLLASPVLAPDFDANGALRIDDPTHNVPGGQGSLVYKDRGAFDRGDLAPPRGIVITPLDNSRDGSDADPVTDSVQISQSNKNYFEILLVDGGEPANPRGGVGINDATVTSDALLLFEDNVPLIEGEDYIFAYDSSGDIIRLTPLAGRWKEDSVYRIELLNDAQAVLKSLDSGSYTDGQQIRLIDGNSVETPFEIERGIILTVPALPGDFANVNDGETFVIFDGVSQRTFEFDTNGSAFAGNVAISIPPSTSTGEPQSANQVSAAIAQAIQLSGLGLQVVDLNGEVQLFSSNRLTSVDTGTSTLGVEGSVGVTTGFGIQIPNNLGLAEGVTDGQQFSIRRGDGRIRFFEIDLNGSVNNTSATPIQISSTTDLTSIATSIRDAILLSDLGLNPEVVDGGQILLPDAADVTLDLVDSVFTQVGQPGDEAAVPIVLAGNLTSEEVGQVIVSSIQSADLSGVSLRVIGDQIIVKGAQAVTGAGAARVQAISDNAGNTLSSNDPLTGTTQFTIFVSSEAGLDYGDAPAEYGTLEANNGPRHTVTPGFSLGSTATPESDARLGTDTSAADGDIDDGIAFANGAVVTPSGTAAVEINLNNSLGLNAILDAWIDWNQDGQFSDSERVVWSPGPIVASTGGIQLQDGDQTYSIAVPATAKPGTTYGRFRLSSNGVSSPLGKVNDGEVEDIVVNVQASTHQNPTNALDVNGSGDVSPIDALQIINAIARYGSGPIDSSVPAFPYVDVNGNGQLEPLDALIVLNYLNSTAAAGEGESAGWIPAANGVLTPEFMQPQAEPETIAAKQSTPATAQTASVFDSPTSGSLDDVIGELASEQATEEPSAIDDFFANLSFE
>NZ_CP036292.1|WP_145117537.1|698595_699339_+|tetratricopeptide-repeat-protein
MHSFRKSQLKCPLTAAALFVLSLSGCQFAASGQNAQGVRLYEQGQYSAALQQFQQAIASDPKNPDSYYNLAATTHRLGKERNDRSLLDQSESLYNQCLDLDPSHVDCHRGLAVLLVETDRPDRAFALMRNWATSQPQLADARIELARLYQEFGEGETAQKFLEDAIHQDGNNARAWLALGQIREAAGDYQQALQDYQRSYDLNSMQPQVAERIASMNRQIVSGAGGVTASGTRLAQQSAADVSKGRY
>NZ_CP036292.1|WP_145117538.1|699670_700858_-|lipid-A-disaccharide-synthase
MNRSIFFSAGEPSGDQHSARLIDALRARDPQLRFRGFGGSEMEQAGCQIDFELTQLAVMGVVEVAPKIAEFYRVAQQAKQIFAQEPPQAVVLVDFPGFNWHIAKRAKACGIPVYYYLPPQLWAWAPWRLRKVRKYVDKVLCVLPFEYNWYRDRGIDAEYVGHPFFDAVAKQRLDRPTIERFDQLKADGKRLVAVLPGSRRGEVTKNWPLQLEAIRRLTKRHPDVRFQVACFRDRQCLWCREQLTAEDQSLPLDFFVGKTSEIVEAAESAIMVSGSVSLELMARSTPAVVLYRVGRILKALASVLVSTKSMTLPNLIAEKTLFPEFVSAGDPEPVIREVVAAADRMLSEPEYLADLQQQLQTLRSKYAAPGASERAAAELIELMGDHREPPIRRAA
>NZ_CP036292.1|WP_145117539.1|700997_701480_+|hypothetical-protein
MNLPESPDYLNSLQGGWEALGNGAPTLVALAQLCARSMVEGTRDKTPLSVEAKAILYAARNRGVIEVRGVNTAFEATARLLAVYIEEGEHRTIAFRNRERPQVTVRFFEAFCQLCRHGLVLHHLYRDFSLTDRGFAIAAKIEREEVAEALGEATEFGLHD

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Crispr_ID: NZ_CP036292_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_6

699587-699664

Orphan

Consensus_repeat	Method
CGCCACTCGCTTGCGCTTCGTGCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_6

>merge|NZ_CP036292|6|699587-699664|CRISPRCasFinder
CGCCACTCGCTTGCGCTTCGTGCTCGTATCTTGGGCTCATTGAGTGACTTCTTGCGTCACTCGCTTGCGCTTCGTGCT

>NZ_CP036292|6|6|699587-699664|CRISPRCasFinder
CGCCACTCGCTTGCGCTTCGTGCT	CGTATCTTGGGCTCATTGAGTGACTTCTTG
CGTCACTCGCTTGCGCTTCGTGCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145117535.1\|679360_681937_-\|carboxypeptidase-regulatory-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|366080
NZ_CP036292.1\|WP_145117531.1\|670621_671437_-\|histidinol-phosphatase	unknown	unknown	gnl\|CDD\|238819
NZ_CP036292.1\|WP_145102576.1\|708399_708771_+\|response-regulator	unknown	unknown	gnl\|CDD\|381093
NZ_CP036292.1\|WP_145123976.1\|705932_708152_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|199834
NZ_CP036292.1\|WP_145123974.1\|673936_674362_+\|YraN-family-protein	unknown	unknown	gnl\|CDD\|237119
NZ_CP036292.1\|WP_145117529.1\|667611_668901_+\|VCBS-repeat-containing-protein	unknown	unknown	gnl\|CDD\|379232
NZ_CP036292.1\|WP_145117538.1\|699670_700858_-\|lipid-A-disaccharide-synthase	unknown	unknown	gnl\|CDD\|234580
NZ_CP036292.1\|WP_145117543.1\|710118_712131_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379155
NZ_CP036292.1\|WP_145117542.1\|708786_709191_+\|aspartate-1-decarboxylase	unknown	unknown	gnl\|CDD\|376751
NZ_CP036292.1\|WP_145117536.1\|682141_698104_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366080
NZ_CP036292.1\|WP_145117530.1\|668870_670295_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP036292.1\|WP_145123975.1\|703502_705722_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036292.1\|WP_145117533.1\|672346_673771_+\|threonine-synthase	unknown	unknown	gnl\|CDD\|235757
NZ_CP036292.1\|WP_145117540.1\|701611_702460_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117539.1\|700997_701480_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117537.1\|698595_699339_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145117532.1\|671414_672116_-\|signal-peptidase-II	unknown	unknown	gnl\|CDD\|376504
NZ_CP036292.1\|WP_145123977.1\|712319_713780_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293754
NZ_CP036292.1\|WP_145117534.1\|674406_679071_-\|tandem-95-repeat-protein	unknown	unknown	gnl\|CDD\|333740
NZ_CP036292.1\|WP_145117541.1\|703031_703388_+\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380429

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145117535.1\|679360_681937_-\|carboxypeptidase-regulatory-like-domain-containing-protein	gnl\|CDD\|366080	pfam00404, Dockerin_1, Dockerin type I repeat. The dockerin repeat is the binding partner of the cohesin domain pfam00963. The cohesin-dockerin interaction is the crucial interaction for complex formation in the cellulosome. The dockerin repeats, each bearing homology to the EF-hand calcium-binding loop bind calcium.	1.40666e-07
NZ_CP036292.1\|WP_145117531.1\|670621_671437_-\|histidinol-phosphatase	gnl\|CDD\|238819	cd01641, Bacterial_IMPase_like_1, Predominantly bacterial family of Mg++ dependend phosphatases, related to inositol monophosphatases. These enzymes may dephosphorylate fructose-1,6-bisphosphate, inositol monophospate, 3'-phosphoadenosine-5'-phosphate, or similar substrates.	1.6353e-86
NZ_CP036292.1\|WP_145102576.1\|708399_708771_+\|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.	9.73971e-07
NZ_CP036292.1\|WP_145123976.1\|705932_708152_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|199834	cd10276, BamB_YfgL, Beta-barrel assembly machinery (Bam) complex component B and related proteins. BamB (YflG) is a non-essential component of the beta-barrel assembly machinery (Bam), a multi-subunit complex that inserts proteins with beta-barrel topology into the outer membrane. BamB has been found to interact with BamA, which in turn binds and stabilizes pre-folded beta-barrel proteins; it has been suggested that BamB participates in the stabilization.	6.12305e-09
NZ_CP036292.1\|WP_145123974.1\|673936_674362_+\|YraN-family-protein	gnl\|CDD\|237119	PRK12497, PRK12497, YraN family protein.	2.83893e-35
NZ_CP036292.1\|WP_145117529.1\|667611_668901_+\|VCBS-repeat-containing-protein	gnl\|CDD\|379232	pfam13517, VCBS, Repeat domain in Vibrio, Colwellia, Bradyrhizobium and Shewanella. This domain of about 100 residues is found in multiple (up to 35) copies in long proteins from several species of Vibrio, Colwellia, Bradyrhizobium, and Shewanella (hence the name VCBS) and in smaller copy numbers in proteins from several other bacteria. The large protein size and repeat copy numbers, species distribution, and suggested activities of several member proteins suggests a role for this domain in adhesion (TIGR).	1.72589e-07
NZ_CP036292.1\|WP_145117538.1\|699670_700858_-\|lipid-A-disaccharide-synthase	gnl\|CDD\|234580	PRK00025, lpxB, lipid-A-disaccharide synthase; Reviewed.	3.66116e-103
NZ_CP036292.1\|WP_145117543.1\|710118_712131_-\|hypothetical-protein	gnl\|CDD\|379155	pfam13385, Laminin_G_3, Concanavalin A-like lectin/glucanases superfamily. This domain belongs to the Concanavalin A-like lectin/glucanases superfamily.	2.06038e-20
NZ_CP036292.1\|WP_145117536.1\|682141_698104_-\|hypothetical-protein	gnl\|CDD\|366080	pfam00404, Dockerin_1, Dockerin type I repeat. The dockerin repeat is the binding partner of the cohesin domain pfam00963. The cohesin-dockerin interaction is the crucial interaction for complex formation in the cellulosome. The dockerin repeats, each bearing homology to the EF-hand calcium-binding loop bind calcium.	7.0967e-07
NZ_CP036292.1\|WP_145117530.1\|668870_670295_+\|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.	9.56648e-10
NZ_CP036292.1\|WP_145123975.1\|703502_705722_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	2.45017e-19
NZ_CP036292.1\|WP_145117533.1\|672346_673771_+\|threonine-synthase	gnl\|CDD\|235757	PRK06260, PRK06260, threonine synthase; Validated.	2.96086e-141
NZ_CP036292.1\|WP_145117542.1\|708786_709191_+\|aspartate-1-decarboxylase	gnl\|CDD\|376751	pfam02261, Asp_decarbox, Aspartate decarboxylase. Decarboxylation of aspartate is the major route of beta-alanine production in bacteria, and is catalyzed by the enzyme aspartate decarboxylase EC:4.1.1.11 which requires a pyruvoyl group for its activity. It is synthesized initially as a proenzyme which is then proteolytically cleaved to an alpha (C-terminal) and beta (N-terminal) subunit and a pyruvoyl group. This family contains both chains of aspartate decarboxylase.	2.26305e-68
NZ_CP036292.1\|WP_145117537.1\|698595_699339_+\|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.	2.72436e-12
NZ_CP036292.1\|WP_145117532.1\|671414_672116_-\|signal-peptidase-II	gnl\|CDD\|376504	pfam01252, Peptidase_A8, Signal peptidase (SPase) II.	6.08111e-29
NZ_CP036292.1\|WP_145123977.1\|712319_713780_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293754	cd16030, iduronate-2-sulfatase, iduronate-2-sulfatase. Iduronate 2-sulfatase is a sulfatase enzyme that catalyze the hydrolysis of sulfate ester bonds from a wide variety of substrates, including steroids, carbohydrates and proteins. Iduronate 2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in the iduronate 2-sulfatase gene that result in enzymatic deficiency lead to the sex-linked mucopolysaccharidosis type II, also known as Hunter syndrome.	0
NZ_CP036292.1\|WP_145117534.1\|674406_679071_-\|tandem-95-repeat-protein	gnl\|CDD\|333740	NF012211, tand_rpt_95, tandem-95 repeat protein. This 95-amino acid repeat occurs in tandem in proteins that may be several thousand amino acids long.	1.00739e-16
NZ_CP036292.1\|WP_145117541.1\|703031_703388_+\|cupin-domain-containing-protein	gnl\|CDD\|380429	cd20295, cupin_Pac13-like, monomeric dehydratase Pac13 and related proteins, cupin domain. This family includes a small monomeric dehydratase Pac13 that mediates the formation of the 3'-deoxynucleotide of pacidamycins, which are uradyl peptide antibiotics (UPAs). Pac13 is involved in the formation of the unique 3'-deoxyuridine moiety found in these UPAs; it catalyzes the dehydration of uridine-5'-aldehyde. The similarity of the 3'-deoxy pacidamycin moiety with synthetic anti-retrovirals, offers a potential opportunity for the utilization of Pac13 in the biocatalytic generation of antiviral compounds. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold capable of homodimerization.	7.97034e-49

>NZ_CP036292.1|WP_145117537.1|698595_699339_+|tetratricopeptide-repeat-protein
MHSFRKSQLKCPLTAAALFVLSLSGCQFAASGQNAQGVRLYEQGQYSAALQQFQQAIASDPKNPDSYYNLAATTHRLGKERNDRSLLDQSESLYNQCLDLDPSHVDCHRGLAVLLVETDRPDRAFALMRNWATSQPQLADARIELARLYQEFGEGETAQKFLEDAIHQDGNNARAWLALGQIREAAGDYQQALQDYQRSYDLNSMQPQVAERIASMNRQIVSGAGGVTASGTRLAQQSAADVSKGRY
>NZ_CP036292.1|WP_145117536.1|682141_698104_-|hypothetical-protein
MAIRKTGSSVNDSSNKSRRSDRAAKRQRLNSRRSLLETLEGRQMLDAGPMLVGVQPDTEPLLQDMAELNTSPREITLRFDELASLDPNSLDGIKIIRAGSDGEFASASAVTDLGSSGAVELTFEAVQSGSAGDNLEIVFTKVSRTDKTLPIVTVAGQRIQIELNSNPALVTRASDIQYGIAQNPDAAALLRVASVSGQTFFDVGRTAQQGQTLTLKGSDRAQATSQLGAANTQVRFTAVASGVAGQDLAIDVRQSFRVAGAPPIVSVIGDRIEVLINSNPASRTTVGQLVTAINAHPQASLLVSAELETGSASSTIGLDLSAFSPIEFSLQNGDLDIEVVPGYVGFVDASQREVVFRFADDLPQDRYRIQIDGTSANALQNTQGDKFNNGVDQTIEFTINSAPTIQAIVPQPIVNGQQLRDQVWVYFDLNDPLDASTVRNTALYQLISTGGTETGADDVTRTPVSVNYNPGTGVAVLQFSGDLYSLFPGTDVKQFRLRVGETDVRGTDPTVLPAVVEPGDSFALARDIRNDWIVSPNNISSVVIEGAIAKTEFINGVPVSNNEYLIDFPGGAGAPGVQEFRPEDPSSYGAPQADALDGISTYFYNFFGQYRGDDPTTATVDDDRVLFNNITEQQKQRVREVLDLYSQYLGVQFVESADMGLQIAVGETLNTSVSWEVSDDLGVINSRLVDESDDDLFGQQFFELATGMVKDLIGVSDFLSPLDASADPLYPSPRDIIEGQYSYRPDSTDIDIYKFSVPTSGEVTIETFAERLAGSASLLDTNLRLYRELSNGTIEEWAGNDDYWSEDSEITVDLPAGTYYIGVSASGNDSYDPMIEDSGLGGLSEGAYELRMSFKPSSATTITDTTGIALDGDNDGIAGGAFDFWFESASFTDTVFVKKDGGTITPMVNNAISGTAKGAVTTISTALSGATSQGTEIIRILPSGDGNLATTADNQPYLIGFDDFGRELADGSSFQVPQDVTVMIDSGSILKLRRARIGVGSSSPVVDFSGGSLQVLGTPLFVGANGSQATVTPVSGDVVFTSLADTSIGGTQSGNVASPGDWGGIDFRSDVDKVDESRIDYEAEGIFLNHVQYGDFRYGGGTILVEAKPEVISPIELSGTRATIANSTFTSNADAAIEASANTFEDDKFTLFEGQATPDYTRVGPSVYNVLFEDNSINGMFIRSQTRDGNGVEKLSVQARFDDLDVVHVIAENLEIQGTPGGAIVESTAPPTRIVRLTATAGGTLPVGEYSYRLSYVTQNGNESPVSNATGTVTTTAANGTIQLEQLPAVPAGSDFVARRLYRSVDGGSYQLVATLNGSSTEFRDTGLAAGAAIDVNRPNVDDVELTATAGGELPAGEYEYKVSYVDANGNELAVSFATEAISVPGIDIDDNTIQLSNLPTSANPSVVARRVYRSFNGDAFRMIALISDNTSTQFTDAGLVSGMTLIENLRPRMDARLAIDPGVIVKLSGAVIEVEQGAQLLAEGTAGQQIVFTSLDDQRFGRGGTFSTNQANANTVFQAGDWGGIYVGPGAQASLDHVRVTGAGGGARIDGKLSFFNPIEVHQGDLRLTNSRVEESGTGFAAGDSDRTGMQTHEAAVIFVRGAQPTIASNTFINNDAVAMNFDLNSLDNTYVSDPGTSIGRLEKVQGTSLGNQGPLVFDNVLENNAINGMEVRGGELATAGVWDDTDIVHVVRGTISIPNHEVYGSLRLESAPDRSLVVKFQSEQSPATIIAGGDASGSAEQFNGLADRIGGALQVIGQPGKSVILTSLSDDTVGSGFDTQGKPQTDTNNSRNDEIGSTTLLLPTGPEIPRGTIIDNDVANDVAGHFSFQPEAGGGVGATVGGGFNEVTTQGANTFFQQQDALFDYLNFIDVGADGAAVELGTTTITTPTTFLSDDVVYSEGTFTGENGLINWRVEQSFEDGSPTLITKLTLSSPTPLGDLRFINYYDPVIASDAGDLLFTEGTPGTNDYRVTVLDGPERVGFRHYGTFEQGTGLEGANYEGWIADEFPDLITDPVFNLPFTPTGTIDTASVPLANVTDLPAPVYGPAITTTAHAWLVNPTATTVTITSALELIEDVFDDTVGLGKPGDWDGIVLREAAHDRNVEAAVEQEGDLSVNRNDQIALAQYLGELAPSTSAGSENRRIGFQVYGNIDQPSDVDVYSFDAEAGTEVWLEIDRTNSSLDSVIELVRVMSSGDDADNDGISDSIVAISNGSISEAIDSGLIIRDENAGSLERTVSSGQVNSLNNSMFTASANSAFNTPQDLYSTNPNDPGLRVVLPGETGEVFTYQVRVRSSNLQLNDPVSKLFSPVTGAKIDEGKYDGLTSGPYELSIRLAESDETAGSYLNLADIRYATTGVSVIGQPFNSPLLGDAVEFIDQAGSDNNDTLATAQQLGPYGTQGDPNSNDSLSIAGAISSDTDIDWFQFSIADSASESSLRNYVSTVFDLDYADGLGRGDFSLWVFDQNGQLILTGLDSNVADDQPGNPNSSDFTSLSRGSTGTADPFIGAVELSAQGDATSNSQTYYVAISGLNNMPSVLDQFTTAAATNPLVRLEPIESLIRIAEDHVSFVGGSTYAPTTLQSLLFDPITAASPLTLNDMKLYVSTSGSADNLRLVNAYTGQNYGTIGTTGGQIFNDIALRANGDLFGYNINGIVDDASWHYFNIDTGFGNVTDLTPTGTNLTTHETLATVDANGNVTRTIVQTDSGVTVNAITFDAVNGAERGFIVGDRGPGNEVIWTNNILWEINPSTGNINGVGLPANPPAAGFAGAYTDPRERGYIETGNPNNLPSTRLGVTAASVVDANGFLAPSLTDGLTFTIRDFVNAGSVLFQFDLGSAIQLSSNVRGGTFLRDGETITVGGQLFEFDTGIRLDVVGSEDPLAGGVAEGSRVTLTSKSTGMAYTFEFDSDGRDFTGRDFSRPDLFAVNLDASTTDASAATILASAINAADIGIRATASNTGEIVLTGATGAATTIGLGVSSLGADGITTANATAIVVDEDLSATDLTRAVSDVLRANQVAIATAGTRIDFTDNPIIDLDLDTPLGVGQAISIVGTANTTGGPTVIPFDVDDTAADIGARVVDAIQAAVDSGLLTSVTATVDGNTVAFSGANVLTAAGALDVAGIAPGGQVTGIAVPTSGDMYAVSNAGGLYRIDSGVISPVRVNFTQNIGDYVDTATDLLGINFTGLSAGPENLAGGAYSDLLFGITGNGDIYAFNTRGELQPIFANGASRISTGVAGATGFDFGNLDYNLWHVTSDTFAGSTTPITLPGHGINATFNDTRTATAGGTSWYFGLDDTISTGTLNARTTRVDGTTVNGTYDFAGGAHGELVSNAFSLEGYNSADLPTFYFNYFLETDSDGDRQLEDSLRVYLVDEDGSEFLLSTNSDSATASTVNPNLSVSDVLTLDQAQETFDNTGTWRQARIALDDFAGQKDLKLRFEFSTSGSMEFGQSELQAVTGEEILDGDRFQISGRDYEFVLSPLLTIPAGNQIANGELIAIDDVVYQFTTDASTVLSPNVAVVYDPTQSGEEIAQSLHDAIANYTTVTNTDYDTDQDASQQNDNMSTANILQVPGGQTTINANGSIGTPNGSQQTVDVDMMRMELSAGQTIMLTVTESTLAPALNPIARVFNAQGVELARELSVDGNTVVSFEAPADGTYYIGISGEGNGNYDPTDNLGGRTFGKSGAYSLELVSTRPYDIRVAGDQVILNGTGPALFSANSTIDVVGNDGSSGIPVNINRDMTATEVASAIADAIRDTLGAGQIITQQGGVLSLPGLRINNAGPLNIPVRTGDAFGSPTVEMARDNDHRGVYLDDFIIGFRERGEFVTSAGNTNDFVPNSGFDLNGDDVASTQTGEYQLEIRGASEYVLSQSLPNPVSMFRSFDTNDRLVQGVTLETLSAEELDAAATALADLILLRNNDPTLEDIDPDTRLSFTLSDGQTSITFEFVNEASAIEPLEGSVPIYYSTGVVNPISGESVSETAADIAAKITDAINLPDVQALLDISALSSSGETSATAAAAGDSRINLSGNVNIIENLSGLSSQILGDSRKPGTDELPTVELFAQSTQALALDRRGDSNTGSEEQGVIKIEGVAVSYSSQFGIDLDHGADVGKFMYPKNLVELNSYVDANGVVHAGLAPGVVVQSNLLAYNRSGGINVQGIDTSNGSQRSMVAFDRIVNNTIIGGTISPTESPGPATYDGTTYANGSISFADVVVSYDPSTTTPPALGLQISAEILGVPDYTGGVAEPTPNAGQGAVSLGGGGSITVQFVDNRLVGSGDASPDLEIFEVGNAEPVLVEVSVDGITYTSVGTSVGGANQIDIDRYGFGPNDRISFVRITDQNFGSALDQAVGADIDAVGAITSVPADQFEAGGVGIALSNGVSPTLLNNVFVNNETAIDASGNVVPNHPVVLGANTFQANTVALNDPNSALLDNVLARFVDPFTNLFVSASDSIFIPAQGSDLIDSSINSLADRPQLQIVRETVGLLASPVLAPDFDANGALRIDDPTHNVPGGQGSLVYKDRGAFDRGDLAPPRGIVITPLDNSRDGSDADPVTDSVQISQSNKNYFEILLVDGGEPANPRGGVGINDATVTSDALLLFEDNVPLIEGEDYIFAYDSSGDIIRLTPLAGRWKEDSVYRIELLNDAQAVLKSLDSGSYTDGQQIRLIDGNSVETPFEIERGIILTVPALPGDFANVNDGETFVIFDGVSQRTFEFDTNGSAFAGNVAISIPPSTSTGEPQSANQVSAAIAQAIQLSGLGLQVVDLNGEVQLFSSNRLTSVDTGTSTLGVEGSVGVTTGFGIQIPNNLGLAEGVTDGQQFSIRRGDGRIRFFEIDLNGSVNNTSATPIQISSTTDLTSIATSIRDAILLSDLGLNPEVVDGGQILLPDAADVTLDLVDSVFTQVGQPGDEAAVPIVLAGNLTSEEVGQVIVSSIQSADLSGVSLRVIGDQIIVKGAQAVTGAGAARVQAISDNAGNTLSSNDPLTGTTQFTIFVSSEAGLDYGDAPAEYGTLEANNGPRHTVTPGFSLGSTATPESDARLGTDTSAADGDIDDGIAFANGAVVTPSGTAAVEINLNNSLGLNAILDAWIDWNQDGQFSDSERVVWSPGPIVASTGGIQLQDGDQTYSIAVPATAKPGTTYGRFRLSSNGVSSPLGKVNDGEVEDIVVNVQASTHQNPTNALDVNGSGDVSPIDALQIINAIARYGSGPIDSSVPAFPYVDVNGNGQLEPLDALIVLNYLNSTAAAGEGESAGWIPAANGVLTPEFMQPQAEPETIAAKQSTPATAQTASVFDSPTSGSLDDVIGELASEQATEEPSAIDDFFANLSFE
>NZ_CP036292.1|WP_145117535.1|679360_681937_-|carboxypeptidase-regulatory-like-domain-containing-protein
MSHPLRLSRRRNSRNRCALQVEHLESRQLLAGLPLGATAADTGEYFLGRVAVTPVLIESDGSIDTSTQDWSETEIAATLAKVTEGVQWWADTLDQLDTVHSLEFVIDDSFATTPYESPFEPIDRPSDDYQVWISQFLRDVGHADVDSLEQGIREFNDAQRQKLDTDWSFTIFVAASDPNGQFAPGGSFSTAFALPGGLFFVSPASRPASTFAHETGHIFYALDEYAGGASAYRTRGYYDSQNLNAINNNPDPGFVQEPSIMSGGTSLQTAYVNHTSSAATLALVGWQDSDGDGIFDVLDVPLTLSGSGRFDSTTGTYRFQGSAAAQALPNQNSTGLQNDITLNEISRIEYRIDAGDWLIASQPNAQTATLDLRIAIDVPFNLIEIRAIDQQTGITSNLFTGSSDLPATTESSAAIAGHVWLDRQNDSEFDAADPGVADVSIQIVDQLGQPVSLIQGVEPDDYPAAAIPATPGVTLSAVGTSISETISASVSQFATTGEQVFAAFNTAQFRNSESWSSARDQIFQATFDEPVASVWIDATALASPSYARIEAYDASGELIHRITSDAIAVETSTTLQISTATRQIASIRAYGHAETSIALDNLRFGTETATSTDNLGTFSLNGLPDGQYRLEIESDRPEIYQVETPLIDIEVVDGVAQAFAAVRVTQLTSPWQNPTDRYDVNASNSIEPLDALQILNEINRSGSRQLTASDIGSRYYDVNGDGMIAPIDVLQILNELQRNPADAGEWYADAGSEPQTGSQTDGDSASAPFAAAVSARFQTADAATQVAEGEHEQATDKFFAALSSASFAGTMGQHPKAGQPVAPLNLEQFASPEETDEPKNSLESESGPLEPLIQPLQK
>NZ_CP036292.1|WP_145117534.1|674406_679071_-|tandem-95-repeat-protein
MAMNQLRQRFLKSRKKNSSRQRRKLFGEALEGRRLLAADIAVPMDGLNPHHNYIFGTDTNRDYQTTAVDALIVINRLNSASASASGELGSTNEDGVFPDVNNDGLITPIDALNIINTINRGEGELAAVLKLSLDVSQDNQSLLRDTGASTTANPMTTRDFELEVGEKFNLEVRWTHFGNDPFSKPLGAFTVYADILANNKDVFAPVLSETQILTISENLVDARSGNFELSFPGGDTATVSLADVAANGFENALASGIEEAGNFESGSISVFPSGVRSTREQNEETGVGDPYQFVVRYNGDNEEFQNIPALNVVANFSDAGGQALTIDATTAEIPVYLNNNQADGLNPDAFRYNIDFRSSNLNESALYTSSPSGNYTLTGDGNPDGDDVIFDEVGGFSNNISPGGLPTIVPNPNQYNGQDFEAYSLELVVVQPGDVTFSLNMPDLVGNQLTVFGSDEALTEDGLVEIDLSENGEGLVRGTFVAPPQDITIGADSITAVEDTARTFDPVANDTEINGGTLTLKSTDGFTQPTNGTVTRDGSTNTLTYTPDANYNGPDSFTYTVVNSEGVEATGVVSITVSAVNDPPTAVNDSGTGLTTPETDSLTITAARLLANDLKGPANESSQTLTVTGVSSTSSKGASVSFNSSTSEILYTPLSGELGNDTFTYTISDGAGGTATGTVTVNVTDVNTPPVAVNDTIAVTEDVPLTIDVSDLLANDSDDNNILSIASVTAGSGASAGSVVLNSGAGTITYTPAANVFGSNADSFTYTLTDGVNPGVTATVRVNITGVNDAPVATDDALTVDEGLTPRTLDVLDNDNAGPGEGTSVTITDVTALPAGAGTIAIAGDGQSLIYTAPSANYVNTAIDFSYTIQDSEGLSATADVTLSVVPTVRPRAIPDVVNINEDSGAIDINVLSNDLGNVGESVTLESIDTTGFPAAAGTLAIDDNGTATKTDDVVTFTPAEDYFSTSGLTFTYTISDTSGDDSAAAAIGANTATVTINVASVNDKPVFGADGLFQIDEDETFTLPASVLANDSAGPANEQQTLAISAVAATSAAGGTVTLDGGVVTFQPAADYHGNDSFTYTISDGVDTTTATASFSIASINDAPNLQPVTQLTQGSEAITLDRSTLLSGATPGPADESSQTLTIFAVSNGGTTSGGGTVVLNADQSVTYTPVAGFSGTDTFEISVRDNGSPSEFSIATVSITNNAAPVVGNDTVSTYKGLTKTILVSDLLANDSDAEGDTLTITSITQPSVGSATLSADGTTITLTTPSETSAEETSFTYTVTDSFSDRVGTVAVEILPFQPSTISGSVYVDQANGSEPNGSQDEGEVGLGAVWVTLTQEGSAPQSVLSDAYGNFVFENVAPGDYTLSYAPPSGVVDSASNPNSISLSIAPAGGETYADISFTADSFNATAGNTLDRYIGSYLMALQRANPSMTTADLDALAQQGIVFGLNTSGDMTFMYVKGGSGFDSTAAISATLSEDGNQLELTKLYADGRVSDPVIIQRALFISVADPDTGDTVIRVLGNVNFVPSITAEGEADFSDYTQAVDQIFGGL
>NZ_CP036292.1|WP_145123974.1|673936_674362_+|YraN-family-protein
MRRFDDWRFGKIDLSRPLGERGEQAAERYLRKLGYRIVSQNDRQGIGEIDLVAVDKRTVVFVEVKTRTSDHRGHPADRIDADKERRLTRAALSFLKRHRLLEHRARIDVIAVWWPPGLEQPERIEHYQNAVEPTGQYQWFS
>NZ_CP036292.1|WP_145117533.1|672346_673771_+|threonine-synthase
MLQTKPSHRKTEGIALQKCISPSCGATYEAESVRTSCDRCGDLVDVIYDWDRGTVPAKLKDFEQFWTQRHDRLRFSGVWRFKELLPFAPDDKIVTVGEGQTLLQQAESVAQYVGMNAGQLYLQYEGMNPSGSFKDNGMCAAFTHAHMMGAKRAACASTGNTSASLAMYCAVSQLMKAIIFVGSGKIAYGKLSQALEYGALTVQIAGDFDDAMIRVKQVSDELGIYLVNSVNPFRLEGQKTIMFRVLEALQWEVPDWIVVPGGNLGNSSAFGKAFTELKELGLIDRIPRLAVINASGADTLYELYERRGVRWNGGNVDMDPIRAFYDEMDRDGAKADTIASAIEINRPVNLKKCLRALEACDGVVRQVSDQEILDAKAKVGAGGIGCEPASAASVAGAKMLRREGVIAPSDRVVCILTGHQLKDPTATVAYHTTDQAVFNDVLGSRGVQRASFANRAVALPNDLEEIIKAIRLYS
>NZ_CP036292.1|WP_145117532.1|671414_672116_-|signal-peptidase-II
MLSPNGDPQVLANAPADRSNPPPQSRDGSPLPHSNPLPAIPTNRYITFFALAILGAVADLWTKQAMFAWRGLPGMRPPHWVVEGYVGIETAVNIGAVFGIGAGKGQLFAAISVVAAIAIFVWLFVKRAAHQWLLTIALGCVMGGIIGNLYDRLGLWWEPGMDPRWQSGVRDWILFQASDTLKWPNFNIADSLLVCGAAMLIYRSFFPVDEFDDDKPNSQEDSNEAHRDNNSSQ
>NZ_CP036292.1|WP_145117531.1|670621_671437_-|histidinol-phosphatase
MTTTPPSEWSARDEGRVAAMIDLAHAAGQLTLNFFGDATLAVDRKGDASPVTEADRSAERLIRQRVAESYGDDAILGEEFADTQGSSGYRWIVDPIDGTKSFICGVPLYSTIVAVEKDDQVIAGAIVIPALGESIVAAIGSGAWHRRNSDADWTAAHVSPCDRIEDAVFLTSQVDSFANRGAAAAYDSLQSAASITRSWGDAYGYLLVATGRADIMVDPIVNPYDVAAVQPVLTEAGGQFSDWKGNPTIRGGDAFGTNGKLHAQVLSHLGG
>NZ_CP036292.1|WP_145117530.1|668870_670295_+|tetratricopeptide-repeat-protein
MDQSRRGKTMKRLKQLLIVILVLEVIFCGIYVKRRLWNHHVVLPAVTLDDPLLAAEFQQLADQATAGGSAEWQALGEGLLGQGFYGEAEHAFRAAVDIDPSNYLAHFALAFCLDRTGRIAESSEEYLKAAEIQRKSKQLVGSVEHCLYQVGKNHLREEDAAAAIDSFASQAGFAPASYQYAKLLVRDGKVDRAMPVLKMELDKTPLSLKFNALRLQALESTGQQRLADEAADVLQRSQYQIPIDLNTDYVTPMNQRLGISRQLQEYNELLASGDMDLLAKHLQSMWDVVEPTTLNQKSKILISMAEVAFQRRRAEEMLHAVDRLKELGVSSPDMLQLEGAAYQLNGDIDRAIALWIRASEMSPNIPLHQILADAYQQKNDDARRDYHRGQAALLEAKLAYWNNQWEPAKQAAQRAIDVDPSLDQAWFYLAEIERELGNPQPALEAYQKCLDLNPNHGRALAAESRLGEKAVDSE
>NZ_CP036292.1|WP_145117529.1|667611_668901_+|VCBS-repeat-containing-protein
MSQIAVLLLLILAVPLVAVYVPSVVGSLSPLPVVFQGGTTCPASSVQFDQVALGGTSVGLPQITNVQVLDFDGDGANEVLACDSLKNQVVLFRQVDGEWQEEVLVPDVAAPAHATAVDIDSDGDLDLVVSVLGNILPDDSVIGRVELFEATPDGYRRHVILDDVRRVADVQPADFDGDGDIDLAVAVFGYSRGSVLWLENRGELKFRDHLLHTAPGTIHVPIADYDGDGDLDIAAIVTQDEEELWGFENLGQGEFKKRRLWMTINHDLGSAGLVQADLDGDGDPDLILPAGDNLEDLDAYPQPYHGCYWFENQGDWTFQIHRISDLGGTYAADVGDFDSDGDLDVVLASMTNNWNRTDTASLVWLENDGQQNFTTWQIASDPIHLVTVAAGDLDGDGSDDIVAGALNLRKPFQRVSRVSAWINQGEGKQ
>NZ_CP036292.1|WP_145117538.1|699670_700858_-|lipid-A-disaccharide-synthase
MNRSIFFSAGEPSGDQHSARLIDALRARDPQLRFRGFGGSEMEQAGCQIDFELTQLAVMGVVEVAPKIAEFYRVAQQAKQIFAQEPPQAVVLVDFPGFNWHIAKRAKACGIPVYYYLPPQLWAWAPWRLRKVRKYVDKVLCVLPFEYNWYRDRGIDAEYVGHPFFDAVAKQRLDRPTIERFDQLKADGKRLVAVLPGSRRGEVTKNWPLQLEAIRRLTKRHPDVRFQVACFRDRQCLWCREQLTAEDQSLPLDFFVGKTSEIVEAAESAIMVSGSVSLELMARSTPAVVLYRVGRILKALASVLVSTKSMTLPNLIAEKTLFPEFVSAGDPEPVIREVVAAADRMLSEPEYLADLQQQLQTLRSKYAAPGASERAAAELIELMGDHREPPIRRAA
>NZ_CP036292.1|WP_145117539.1|700997_701480_+|hypothetical-protein
MNLPESPDYLNSLQGGWEALGNGAPTLVALAQLCARSMVEGTRDKTPLSVEAKAILYAARNRGVIEVRGVNTAFEATARLLAVYIEEGEHRTIAFRNRERPQVTVRFFEAFCQLCRHGLVLHHLYRDFSLTDRGFAIAAKIEREEVAEALGEATEFGLHD
>NZ_CP036292.1|WP_145117540.1|701611_702460_-|hypothetical-protein
MKRAILSTTLIIGMSICSQGFGFDLLDRMLGLKCGGGSSSCCETGCADVCEPACGCETSCCESVCEPACGCEASACGTSCCEPTCGVESSLCGASCCEPACGCETSCCEPACCDSKSCFGSKKKCCGLLSKLFGGKKNGCDSCCETSACCEPACGCEAAACCEPACGCETSLCGSASCCEPACGCDPCGKKKSGGLLSKLFGGLKCCKKSDCDSACDSCGCAGSYAAPAAPACSSCNGGTSVQVEAPVVEDAAPMPPAPVVDPSAYLNSKRRVIQASTRYAR
>NZ_CP036292.1|WP_145117541.1|703031_703388_+|cupin-domain-containing-protein
MPKAPAFVVAHLPDLPGTPCPCGTARRAFAEVESFPATVHLTEIAATAKVHYHKTLTETYVVQECDDDAFIELDGQAHPVRPGTAILISPGTRHRAVGKMKVIIFCTPKFDPNDEWFD
>NZ_CP036292.1|WP_145123975.1|703502_705722_+|PQQ-binding-like-beta-propeller-repeat-protein
MRTYLLILPTLLLLAGAAFGQAPKAADWSYWRGPNYNGTSSATGLPATWDPDGGEGSNLKWHRDDLAGRSTPVAMDGKLYLITRADPGTEIEGERVVCIDAATGETVWEHKFNVWMSDVPDTRVGWASVVADPETGNVYALGVCDIFMCLDGKTGEEKWSVPLHEFLGMLSTYGGRTNFPIIHEDLVIISGIIINWGDAAKPNHRFLAMDKRTGEIVWFSPTRDLPDDTSYSAPSLAVINGQLQMVVGGGDGAVWGFQPRTGKTLWNYQFSRRGLFATPLVVGNRVYAGHGEENMEGTSMGALAAIEIEGTGSDTKAKELWKMEGLILNRSSPLVIGDRLYIVDDRCKLWVVDAKTGEMIQERVALGDRKQWASLVYADGRIYAVTENGRWAFMELSDAGVDITDKGRISNEAFYASPIVYDGAIYFVGTSGIYCIADEKAKPGVAPAPEAAKEMANDDKTPAWVQVVPAEAIVRPGEKIDYKVRLFNQNGQFIEEASDPKLTVVGGGSVDGTTFDAADQNGSHYAATVTATVGDLQGSSRVRVVPALPWKFTFDELDDAPVTWVGARYRHVIREVDGSPALVKVSTIPKGARSRGWMGHWDLANYTISADVKGQQVGTQLPDIGLTAMGYALDLQGNSQKLQIRTWYAQLRMAKTVPFEWKADVWYRMKLQAGIEEQDGKKVAVLKGKVWPRDDKEPSEWTVTAVDHSPNLSGSPGLYGNAKVCELYLDNIEVTANEQ
>NZ_CP036292.1|WP_145123976.1|705932_708152_+|PQQ-binding-like-beta-propeller-repeat-protein
MSGCRKPTDPAGVSSNTTADDSNVTAADSNVTAAETPIAAADDNEATAEMQLKAVDTPVAAKPAAAEVKETPVAEVKEAPAAEPKEAPVAEAKEEPAVKLAAAPKATKTAAAPAGKSDDPAAVLEAGGDWPQWAGTRLRNNTPNVKGIAKSWNIGKFDRRTGEWDGTNAENIKWFAKLGSQTYGNPVVAGGRVFCGTNNSGGYLKRYPGDIDLGCLICFDEETGEFLWQHSSEKLITGRVHDWPLQGICCAPLVEGDRLWFVTSRGEVRCLDTKGFHDGSDDGEVKGERGRVADLPVAKPEFKEAVAGLDKGELTQALLDLLTEHGEPIEGTAEVTTVAAGKKWSIKATIDGAARDLEAVVAGPRLSVFKTITADDKEEADVLWVYNMMEELGISQHNMCSCSVTSYGDLLFVNTSNGVDESHIVLPSPDAPSFICMNKNTGEVLWTDKSPGTNIVHGQWSSPTVAELGGVVQAIFAGGDGWVYSFKADQGGDGNPELLWKFDANPKTSKWILGGAGTRNNIIATPVVHDGLVYVAVGQDPEHGEGQGHLWCIDPTKRGDISSELAMKIEGDKRVPIPHRRLQAVIEEDGEVAIDNPNSGVVWHYASFDQNGDGEIDFEEEMHRSCGTVAIQGDLLYVADFSGMLHCLDPKGSENGEPIVHFTYDMLAQAWGSPLIADGHVYIGDEDGDVAIFELGKDNKEPIDEINMGTSVYSTPIAANGVIYISTKDKLFAIAPPKE
>NZ_CP036292.1|WP_145102576.1|708399_708771_+|response-regulator
MMQTVLDIGNCSPDHSAIRTLIEGNFDARVVQAHGAADAMEILGRQEVALITVNRKLDRDYSDGMEIIRQLKNDPKTQAIPVMLITNFPEHQDAAMAIGAERGFGKLQLRAAETKQSLAAFLS
>NZ_CP036292.1|WP_145117542.1|708786_709191_+|aspartate-1-decarboxylase
MPFRKLLSAKIHRATVTGADLEYEGSITIPPELMEAAGIVPYESIQIWNVTRGSRLETYAIEGVRGSSDICANGAAAHHVYPGDKVILATFAFYDRDDAATHCPRLIFVDDHNQIKHEGPEIAGPQRRAEPAGS
>NZ_CP036292.1|WP_145117543.1|710118_712131_-|hypothetical-protein
MTVKPSTARFVASGLLGLCTSLAITSIALSHEGVAGHSHDHKHRANDSFFTTRGKAQVLPLAKEEDVFHFVVYGDRTGGVPEGLKVLEQAVADTNLLSPDLVMTVGDLIQGYNEKPEWMRQMAEYKEIMNQLKMRWFPVAGNHDVYWRGKGPAPAGQHDSNYEQHFGPLWYTFRHKNAGFIVLYSDEGDPVSNKKAFNDGKLQQMSEQQLKFLGEALDRHKSLDHVFVFLHHPRWTGGGYTGTNWDTVHGMMKKAGNVSAVFAGHIHHMRFDGHKDGIAYYTLATTGGHLSAEIPGAGYLHHLNIVTVRPDDISVAALPVGAVMDPKEFTPEFLAEIQAARKVRPQITASDLLLQTDGSATGQVTVKLHNSSPRKMQVTASIDTASRDWLSSLDHDHLTLAAGATETFVVKLRRVADPQASWTIPRITLDRVFVGETARIQLPSVSTPVELDLAAVPADYFTNQTDHCLEVKGEQSAARIASDAIGLPDGPFTLEAWLNPSQSEGMRAAVAKTQQSDYAIFCNEGVPQFDLNLDGKYYSAKAQEKLPVGQWTHVAGVFDGKQVRLFIDGKPISAVDAKGKRKKNKHPLYVGADPDNSGQPTRPFIGKIDEVRLTAEALYSEAFEPAERLMPSEKTHLLLHFDRTLGPYVLDHSPRGSKANLGTKSVLTAR
>NZ_CP036292.1|WP_145123977.1|712319_713780_+|sulfatase-like-hydrolase/transferase
MAGVVICSVLCGGLVAADDVASGQTESVKRPLNVLFIISDDLTLNALSCYGNEVCQTPNIDALARSGTRFTHAYCQGTYCGPSRASFMSGYYPHATGILGYISPRKAIGDRATWAQHFKNSGYYTSRVSKIFHMGVPGGIEKGDDGADDPISWTERFNSQGPEWRAPGKGETLENNPDGKKPAVGGNTFVVVEADGDDLVHSDGRTAEKVCQLIHEHKDEPFFLGVGFVRPHVPFVAPASYHEPFPEAEMQLPEKVAGDWDDIPKLGINYKTSKNMKMDVQRQRKAVAGYYASVAYMDAQVGKVMAALQEAGIADRTIVIFTSDHGYHLGEHDFWAKVSLHEESVLVPLIIRVPGKQPAVCESLTELIDLYPTVSSLCGLEVPKRLQGTDISGMLDDPELELRETAFSVNGKGFLIRSQRYAYIRYRENASGGEELFDMQTDPQQYTNLVDDPAYAATLEKMRAEFAKTMRRVRDNDLAVSPRSKN

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Crispr_ID: NZ_CP036292_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_7

1036648-1036749

Orphan

Consensus_repeat	Method
TTTCGCGGAGCGAAAGGCGACTAACTTG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_7

>merge|NZ_CP036292|7|1036648-1036749|CRISPRCasFinder
TTTCGCGGAGCGAAAGGCGACTAACTTGCGGGGTGGGAGATCACTCGCTGGCGCTTCGTGCTGGTATGCGCGGGTTTCGCGGAGCGAATGGCGACTAACTTG

>NZ_CP036292|7|7|1036648-1036749|CRISPRCasFinder
TTTCGCGGAGCGAAAGGCGACTAACTTG	CGGGGTGGGAGATCACTCGCTGGCGCTTCGTGCTGGTATGCGCGGG
TTTCGCGGAGCGAATGGCGACTAACTTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145117900.1\|1041853_1042315_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145092063.1\|1041349_1041796_+\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|240047
NZ_CP036292.1\|WP_145117882.1\|1032174_1033050_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226218
NZ_CP036292.1\|WP_145117872.1\|1025372_1026734_+\|DUF1598-domain-containing-protein	unknown	unknown	gnl\|CDD\|377890
NZ_CP036292.1\|WP_145117870.1\|1023856_1025119_+\|NAD(P)-binding-protein	unknown	unknown	gnl\|CDD\|366721
NZ_CP036292.1\|WP_145117896.1\|1039187_1039922_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145117894.1\|1038438_1038834_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|272979
NZ_CP036292.1\|WP_145117878.1\|1030243_1030963_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275381
NZ_CP036292.1\|WP_145117884.1\|1033248_1034058_-\|tryptophan-synthase-subunit-alpha	unknown	unknown	gnl\|CDD\|240075
NZ_CP036292.1\|WP_145117898.1\|1039991_1041359_-\|CCA-tRNA-nucleotidyltransferase	unknown	unknown	gnl\|CDD\|223690
NZ_CP036292.1\|WP_145117902.1\|1042514_1043159_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145102636.1\|1043427_1044990_+\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223627
NZ_CP036292.1\|WP_145117874.1\|1027149_1027788_-\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP036292.1\|WP_145117890.1\|1036804_1037560_-\|ThuA-domain-containing-protein	unknown	unknown	gnl\|CDD\|377643
NZ_CP036292.1\|WP_145117892.1\|1037719_1038190_+\|FxsA-family-protein	unknown	unknown	gnl\|CDD\|377238
NZ_CP036292.1\|WP_145117888.1\|1035663_1036533_+\|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase	unknown	unknown	gnl\|CDD\|234899
NZ_CP036292.1\|WP_145117904.1\|1045335_1046622_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036292.1\|WP_145117886.1\|1034208_1035435_-\|tryptophan-synthase-subunit-beta	unknown	unknown	gnl\|CDD\|235288
NZ_CP036292.1\|WP_145117876.1\|1028181_1029621_+\|response-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP036292.1\|WP_145117880.1\|1030901_1032104_+\|cytochrome-C	unknown	unknown	gnl\|CDD\|369445

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145092063.1\|1041349_1041796_+\|NUDIX-domain-containing-protein	gnl\|CDD\|240047	cd04691, Nudix_Hydrolase_32, Members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	6.32834e-26
NZ_CP036292.1\|WP_145117882.1\|1032174_1033050_+\|ABC-transporter-permease	gnl\|CDD\|226218	COG3694, COG3694, ABC-type uncharacterized transport system, permease component [General function prediction only].	1.18694e-35
NZ_CP036292.1\|WP_145117872.1\|1025372_1026734_+\|DUF1598-domain-containing-protein	gnl\|CDD\|377890	pfam07643, DUF1598, Protein of unknown function (DUF1598). A family of Rhodopirellula baltica hypothetical proteins of about 500 amino acids in length.	5.4874e-31
NZ_CP036292.1\|WP_145117870.1\|1023856_1025119_+\|NAD(P)-binding-protein	gnl\|CDD\|366721	pfam01593, Amino_oxidase, Flavin containing amine oxidoreductase. This family consists of various amine oxidases, including maze polyamine oxidase (PAO) and various flavin containing monoamine oxidases (MAO). The aligned region includes the flavin binding site of these enzymes. The family also contains phytoene dehydrogenases and related enzymes. In vertebrates MAO plays an important role regulating the intracellular levels of amines via there oxidation; these include various neurotransmitters, neurotoxins and trace amines. In lower eukaryotes such as aspergillus and in bacteria the main role of amine oxidases is to provide a source of ammonium. PAOs in plants, bacteria and protozoa oxidase spermidine and spermine to an aminobutyral, diaminopropane and hydrogen peroxide and are involved in the catabolism of polyamines. Other members of this family include tryptophan 2-monooxygenase, putrescine oxidase, corticosteroid binding proteins and antibacterial glycoproteins.	3.34325e-46
NZ_CP036292.1\|WP_145117896.1\|1039187_1039922_+\|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.	0.00452627
NZ_CP036292.1\|WP_145117894.1\|1038438_1038834_+\|hypothetical-protein	gnl\|CDD\|272979	TIGR00237, exodeoxyribonuclease_VII_large_subunit, exodeoxyribonuclease VII, large subunit. This family consist of exodeoxyribonuclease VII, large subunit XseA which catalyses exonucleolytic cleavage in either the 5'->3' or 3'->5' direction to yield 5'-phosphomononucleotides. Exonuclease VII consists of one large subunit and four small subunits. [DNA metabolism, Degradation of DNA].	0.00598602
NZ_CP036292.1\|WP_145117878.1\|1030243_1030963_+\|hypothetical-protein	gnl\|CDD\|275381	sd00034, LRR_AMN1, leucine-rich repeats, antagonist of mitotic exit network protein 1-like subfamily. A leucine-rich repeat (LRR) is a structural protein motif of 20-30 amino acids that is unusually rich in the hydrophobic amino acid leucine. The conserved eleven-residue sequence motif (LxxLxLxxN/CxL) within the LRRs corresponds to the beta-strand and adjacent loop regions, whereas the remaining parts of the repeats are variable. LRRs fold together to form a solenoid protein domain, termed leucine-rich repeat domain. Leucine-rich repeats are usually involved in protein-protein interactions.	7.91142e-10
NZ_CP036292.1\|WP_145117884.1\|1033248_1034058_-\|tryptophan-synthase-subunit-alpha	gnl\|CDD\|240075	cd04724, Tryptophan_synthase_alpha, Ttryptophan synthase (TRPS) alpha subunit (TSA). TPRS is a bifunctional tetrameric enzyme (2 alpha and 2 beta subunits) that catalyzes the last two steps of L-tryptophan biosynthesis. Alpha and beta subunit catalyze two distinct reactions which are both strongly stimulated by the formation of the complex. The alpha subunit catalyzes the cleavage of indole 3-glycerol phosphate (IGP) to indole and d-glyceraldehyde 3-phosphate (G3P). Indole is then channeled to the active site of the beta subunit, a PLP-dependent enzyme that catalyzes a replacement reaction to convert L-serine into L-tryptophan.	1.04534e-103
NZ_CP036292.1\|WP_145117898.1\|1039991_1041359_-\|CCA-tRNA-nucleotidyltransferase	gnl\|CDD\|223690	COG0617, PcnB, tRNA nucleotidyltransferase/poly(A) polymerase [Translation, ribosomal structure and biogenesis].	8.26976e-71
NZ_CP036292.1\|WP_145102636.1\|1043427_1044990_+\|DEAD/DEAH-box-helicase	gnl\|CDD\|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	1.21731e-64
NZ_CP036292.1\|WP_145117874.1\|1027149_1027788_-\|response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	3.09757e-65
NZ_CP036292.1\|WP_145117890.1\|1036804_1037560_-\|ThuA-domain-containing-protein	gnl\|CDD\|377643	pfam06283, ThuA, Trehalose utilisation. This family consists of several bacterial ThuA like proteins. ThuA appears to be involved in utilisation of trehalose. The thuA and thuB genes form part of the trehalose/sucrose transport operon thuEFGKAB, which is located on the pSymB megaplasmid. The thuA and thuB genes are induced in vitro by trehalose but not by sucrose and the extent of its induction depends on the concentration of trehalose available in the medium.	6.20281e-22
NZ_CP036292.1\|WP_145117892.1\|1037719_1038190_+\|FxsA-family-protein	gnl\|CDD\|377238	pfam04186, FxsA, FxsA cytoplasmic membrane protein. This is a bacterial family of cytoplasmic membrane proteins. It includes two transmembrane regions. The molecular function of FxsA is unknown, but in Escherichia coli its over-expression has been shown to alleviate the exclusion of phage T7 in those cells with an F plasmid.	8.69429e-32
NZ_CP036292.1\|WP_145117888.1\|1035663_1036533_+\|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase	gnl\|CDD\|234899	PRK01103, PRK01103, bifunctional DNA-formamidopyrimidine glycosylase/DNA-(apurinic or apyrimidinic site) lyase.	9.69499e-84
NZ_CP036292.1\|WP_145117904.1\|1045335_1046622_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	9.32841e-17
NZ_CP036292.1\|WP_145117886.1\|1034208_1035435_-\|tryptophan-synthase-subunit-beta	gnl\|CDD\|235288	PRK04346, PRK04346, tryptophan synthase subunit beta; Validated.	0
NZ_CP036292.1\|WP_145117876.1\|1028181_1029621_+\|response-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	9.79969e-175
NZ_CP036292.1\|WP_145117880.1\|1030901_1032104_+\|cytochrome-C	gnl\|CDD\|369445	pfam07635, PSCyt1, Planctomycete cytochrome C. These proteins share a region of homology at their N-terminus that contains the C-{CPWHF}-{CPWR}-C-H-{CFYW} motif typical of cytochromes C, or CxxCH.	1.18061e-11

>NZ_CP036292.1|WP_145117888.1|1035663_1036533_+|bifunctional-DNA-formamidopyrimidine-glycosylase/DNA-(apurinic-or-apyrimidinic-site)-lyase
MPELPEVETMRRGILPIVGATISSVQRPPCHCRPISIKPRIDHLDRRASGRKITDIDRLGKRVVIHLDDGQAIVIEPRMSGLVLLADPPGIEHLRLRIELTGVTHRELLFWDRRGLGTVRLLSTEELRALVTERLGPDALQISADQLRGALRASRRAIKVALLDQSVVAGIGNLYAAEILHLAGVDPRTRCDQLSGPQWQRIQAAIGQILETAIRHEGSTLSDGTYRNALNDPGNYQSQHQVYDRADQMCYRCDRGPITRIVQAQRSTFYCPTCQQKRGLHESLADYRS
>NZ_CP036292.1|WP_145117886.1|1034208_1035435_-|tryptophan-synthase-subunit-beta
MSGTLPKALSPQSVPDSAGRFGSFGGRFVPETLTRALDELVAEYDKAKADPSFQEELDGLWKTFVGRPSPLYFARRLTEACGGAQIWLKREDLNHTGAHKINNTLGQALLTLRMGKTRVIAETGAGQHGVATATACAHFGLPCVVYMGAEDIRRQKPNVFAMKLLGAEIRAVESGSRTLRDAVNEAMRDWMSSVEDTHYIIGSVIGPHPFPMMVRDFQSVIGREARVQSLEAFDGKLPDCVVACVGGGSNAAGIFAPFVADDGVRLVGVEAGGRSSEPGQHASPLTFGRPGVLHGSYSYVMQDDDGQTCDVHSMSAGLDYPGVGPEHSYWKDTGRAEYIQCRDDEAMKAFDMLAKSEGILPALESSHAIAKGMEVAGKMSPDQNLVICLSGRGDKDAMELARLRGEEW
>NZ_CP036292.1|WP_145117884.1|1033248_1034058_-|tryptophan-synthase-subunit-alpha
MSLLDETFAKLRSEGRKALLPFITAGDPDLDFTGDLLKDFGKAGVAACEVGVPYSDPVADGPVIQASYQRALESGFRLQQLFEMRKRVAAEVTIPTLTMASYAIIYRVGLERYIEQSQEAGFCGVIVPDLLVEEAAEFSKLCADRDFNLIQLVTPTTPRERQVRIAESSSGFLYFVSVTGITGERNELPPQLIDNVGWLREQTDVPVCIGFGISQPEHVAKLGPVADGLIVGSAIVRRIAQANAENRGEVRGEIDRYVREMLAAINAVK
>NZ_CP036292.1|WP_145117882.1|1032174_1033050_+|ABC-transporter-permease
MKSTMAEPNQGPHYGRVLLTFARNSLVRDMTFRANFLFQCISSVSWTLMNVGFYLIIFQYTNSIGEGTGWHKHQFFLFLATTWFINSLVQAFFMPNAEEFSELIRTGGLDFALLKPIDTQFLVSFHKVDWSSLSNFAVGLVLAAISLSYLITDPVAPLQITATMVILYPLFILCGVAIMYSLMISLSATSIWLGRNQTLYNFWFYITNFSRYPMEIYQNGWGWSLWGLFTFVIPVLVVVNVPARIIAKPLDPRAAWEWPLAGFMLFATVVCLVASRWVFRKALLSYRSASS
>NZ_CP036292.1|WP_145117880.1|1030901_1032104_+|cytochrome-C
MSISIKPTMTSIPVNTIRTINSGAQTVASPGDAGNRVSRQVQNRLQCIESARQKSRCFSLLPHRLPALSHLKITAMKTNKFLGIVFCLAFLSSSAAIAAGPLNADGQVIDFQRDVAPILRTKCLSCHGPDDAKNDFRVDDPEIMADYIEAGDHESSSLYIDYIVAEDPDMLMPPESEGPMSPAEIAILRLWIEEGANWPEDAQVVLSDPAAVDVVIVEPVPVPDSLASRVWAFQGYLHPATVHFPVALLTFGAAFVVLGYKWPQLAHPIPFACLLCGALSAIAASAMGWSFADQEGYGSWSKGLEASISRHRWTGVGVTITSVAFALIAIKAEMNENLRLRKVWQIGLLISAGMVGLVGHIGGELTYGEEFYHKAFEILSGTDSELPVIEIETVSTDGES
>NZ_CP036292.1|WP_145117878.1|1030243_1030963_+|hypothetical-protein
MAFLIVAAGCGSQQTPDAVVGESDPPSANTVADPNEQSLAQQIADVEASQSERIFLNAPVVDSDLTQLAQLESLSDLLLDGGAVTDTGIAAIVTCPNLKHLRLRFSPIGDDGLRQIAQLKDLEILNLPHSACTAAGIGELASLPKLRQLRLGSDRATAEICQAISRLESLRSLHLIDIPVDDENLLRLADLKNLRSLYIDGGRVSDAGWQALFAKRSDLHVHIDQTHHDLDPGKHDPDH
>NZ_CP036292.1|WP_145117876.1|1028181_1029621_+|response-regulator
MTLNPKLLLVDDDRRLAESMADWLRFQQFNVDQAHSLAGGRRAIQEQTYDLMLLDLRLEDGDGFALIAETKRRQPDCAILVLTGYATPNTAIEAVQAGAFDLLTKPLVDEELSHALERALAQQNIQAENEKLRAQLDSRFGLEHILSHDYRMLKIFDVIDSVADARASVLITGENGTGKSMIARAVHKRSNRRNNPFVEVACGALPDNLLESELFGHVIGSFTGATTNKVGKFKQADGGTIFLDEIGTASQAFQVKLLRVLQELQFEPLGGTETETVDTRVILATNENLAQAVSSGQFRQDLFYRVNVINIELPALRERSGDVPLLVDHFLREVCETTGRDVQGFDRDALAILQSYAWPGNVRELENVVERAVLLARDSVLTRNDLPPHLLSSSSNPRTASDSFDSPSTLSSDSGSGQTLREALEEPERRIILESLRLHNWNRAATADTLGVNRTTLYKKMKRLGLDDPRLQFMGAEAR
>NZ_CP036292.1|WP_145117874.1|1027149_1027788_-|response-regulator
MKSLDVVIIDDHEVVRSGITSLLSGPEVTVIGSAASGQEGLELMSKQLPDAVLLDIRMPDNDGLSTLQTLRASHPDLPIVMVSTYDNPTYVARSVALGANDYVLKGDSRSVFLDALTRAASGEEPSSDSLLRKIGESMSRSGKEAPPMDVPLTAREVQVLRHVALGLSNKEIGCSLNISVETVKEHVQNILRKLNAADRTDAAVRAVKMGLA
>NZ_CP036292.1|WP_145117872.1|1025372_1026734_+|DUF1598-domain-containing-protein
MTVVFAGLPLTEAYSGDDGGGDDNNQNFNQVAGIEIDAAGVLRVREFSPELTRQRIAAARQQLPPDLARRSPLRKISLQRLEQAVAAKVEAGEKIPEDMLALAGLTGVEYVFFYPEEGEIVLAGPAEGFVEDASGRVRGIDTGRPVVLLEDLVVALRAFPPHEKSNAVISVSIDPTEEGLQRMQQFLASVRGRVRPSDAARLAAGLKGTMGMQNVSFKGVSTSTHFAQVLVEADYRMKLVGIGLEKLPVGLLSYVDRVHPRQVAANAMERWYFVPNYDCVRVSEDENAMQLLGKGVKLIAAGERVGKGGEREATRGVNKASQAFCQDFTNKFEEISRTVVVYAQLRNLIDVSIAAAYIQKQDFYGQAGWEMPVFGSEQAFAVETRTAPVQVETAVNAIWRGSTLMTPLGGGIKLQPRVALNSSRIQPDSEGRAAQAYKSQRTDSLKPGQWWWD
>NZ_CP036292.1|WP_145117870.1|1023856_1025119_+|NAD(P)-binding-protein
MRDNRKKEVIIIGGGLAGLACGVQLAKRGVDFEILEATDRVGGRVRTDIVDGYRLDHGFQVFLTAYPAAQQLLDYDRLQLRPLEPGALVRCGDQFSALLDPRRRPASILASALSPVGSLSDKLRMARLIRDVCRGELEELWEHVAQPTRYRLPGLNFSDRFIEQFLQPLLGGIFLDPELQTSSRMMEFVLRMFAQGDAAVPAQGMQAIPQQLAERIPTDRLQLESTVSEIEGTTIRMTDGSQRSAAQIVIATEGPAAARLLNIDESIPWQQVSCLYFTADEAPLQTKQMILSGETSGPINNLCELSTVAPEYSPAGKTLISVSVLKSDVPAMELHEPVVKQLRSWFGEQVDTWSLLRTFHIPFALPEQSIDRMQTVIKPVQRAGMPIVCGDHRETASIQGALSSGIRAAEAALGGLGDAG
>NZ_CP036292.1|WP_145117890.1|1036804_1037560_-|ThuA-domain-containing-protein
MRLSSIASVLFLCLLFVSGRATAAEPLRALLVTGGCCHDYENQIKILQAGLGKHLKIDWTVEQYDEKRDRKANVYTKPKWAESFDVIIHNECFGGVTDGEFVESIVAEHVRSGVPAVVIHCSMHSYRNAPTADAWRGLIGVTSKRHEKAKRSLKVVAREAEHPILEGFPSPWSTPNGELYIIERSWPNTQVLASAYSDEEKADQPVVWTNTYKGVRVFGTTLGHHNETMQDDVWLNLTAKGIQWATTPDAQ
>NZ_CP036292.1|WP_145117892.1|1037719_1038190_+|FxsA-family-protein
MFLKLLLAFTIIPLVELAMLIQLSKATSLLVTVGIVIFTGIVGSMLARWQGALAWQRFRQALAEGRMPAPEVQDGLLIFFAAGMLLTPGLLTDAMGFLLLIPQTRLLARHFLAVRIGSRFQIQTFGFGENAQPTQSDPNTIDAAAASVRSDKRTDS
>NZ_CP036292.1|WP_145117894.1|1038438_1038834_+|hypothetical-protein
MEPRPKAKQRLQRALELELEQQVQLLQRLLERFRQQHPSTKHMLVQLRRQLRRHSSSIRLQQQERHSSLELECCSSLVLVLRSKLVLVLRSRLELELRSSSVLQPFRSKLVLEGSTCSSSCGLLLPMRRMR
>NZ_CP036292.1|WP_145117896.1|1039187_1039922_+|tetratricopeptide-repeat-protein
MLPFLLALTLLQPVKTIGQWEGEGYRALRDGNLDRVAEIAKKIEDQHPASFSAAMARGSLLLRAGMAKEALIAFDEAAKLQPAQIPYMWQRGIAQYYAGEFVAGRRQFVVHREVNAHDVENAVWHYMCVARVEGVDAARREYLPAPGDSRVPLQEVYDLFAGTATIQTVTDAIDAIPAQSRGAASAQFYGWLYLGMYEDAQGNLAEARKWLEKAVALKQTHYMADVANVHLQQVVARIEKPADK
>NZ_CP036292.1|WP_145117898.1|1039991_1041359_-|CCA-tRNA-nucleotidyltransferase
MCPLRLALVLVEFWKPVVTDSDQPLDPRERFARSVVQKLTDAGHIAYFAGGCVRDRILGLRPKDFDVATDATPDRIRELFGRRRTLAIGAAFGVVSVLGRKGAGEDPIEVATFRSDGDYSDGRRPDSVVFSSPEHDAQRRDFTINGLFYDPIAGRVIDFVDGRSDLQAGVLRAIGDPDARICEDKLRMLRAVRMATVFGFAIESATRDALHRHAAEIDVVSNERVGAEMRRLLAATAAFDGLATLRETRISDVVFPQLAEIWDAEIRQADLPAEIAAPATTGAGLMSKLLVARREYDFVSGLIVCLLAIKWSGGDSGDALRRIADLWRLSNEETARAAFALESLPTVLQADRQPWSIVQPVLAARYAGDAVTLAETVTRALDLPGDAVAAARQRLGWDRDRLDPPALLSGNTLQKLGLTPGPGFREILQDVRARQLDGLLNDAQTAAQYVSATYL
>NZ_CP036292.1|WP_145092063.1|1041349_1041796_+|NUDIX-domain-containing-protein
MDTNKDRADRRQRTGMGVVGVILREDRFLLIRRSKTVTAPGFVCFAGGGVEAGESEQDALVREMQEELAIDIVPTQRIWESVTRWGTELGWWLIEAAHDLDPVPNPAEVEEIFWLKRSEITPRRDLLGSMPDFLGAWQQGAFKLPIDY
>NZ_CP036292.1|WP_145117900.1|1041853_1042315_-|hypothetical-protein
MSNPHRPVSPIFSIDVSAEPPTPASPQFDGDEQVIELLRELVVGQQKQNQLLEQMTQQTAAMQKQRSNELQQWKDANPLLSKHCHRAAETLSRVQTQFLENLTVEVLDNAEHLVDGEFMLNEFVDRFGPRMAHLNGVLQVLAQLGTGQPTSET
>NZ_CP036292.1|WP_145117902.1|1042514_1043159_+|hypothetical-protein
MIASENSPLASVSKAQAVVGVVPIGMIAATLPRQLTMQHECRWRHTILATKKDINLGFYLVQNDETAGWMGGYLVLNSSGRPLEFHCSLPLRPTRTQQILYGPSLGAYLVGDLIGKALLDRAKMKTQLVLADNVDALPLARRSGIPFACTEVSKRANIDDVIEVDGWQAIASPGQRDDVMEILQKLPATFDLNEPFDRIREAFSEARGTSRAAA
>NZ_CP036292.1|WP_145102636.1|1043427_1044990_+|DEAD/DEAH-box-helicase
MWGKKSEEKIVRKKVQPADEIVVPEEDPEPKAKKKKSATRIEPPSDVIKLQDRLYYLLQPPMESLVGSGELNFPFKPFPYQFDGIAFLFPRYAAVLADEMGLGKTMQAISTIRFLLCSGEASSILLVCPKPLVTNWQREFKLWAPEIPVGIVEGDAEKRAWQWRHRATPVKIANYELLMRDRDVVTDPELKFDLVALDEAQRIKNRNSTTSKIVHAISRKRSWALTGTPIENSPNDLVGIFEFLSPGYLNNDMTPLALGKATRDFVLRRTKDKVLTDMPPRLFRDAELDLTPEQWATYQQAEDSGVIQLEEMGKSLTVQHVFELVLRLKQICNFDPATGTSTKMERLVADMEEVAASGHKAIVFSQWVKSIDKMRPALERFGPLEYHGRIPHKKRDGVIDQFKNDPSKHVILMSYGAGSVGLNLQFCRYVFLFDRWWNPAIEDQAINRAHRIGAAGSVTITRMLAMNTIEQRIAEVLDQKRELFESVFSDSASPGTVGLSRDDIFGLFKLRTPEGIVKTI
>NZ_CP036292.1|WP_145117904.1|1045335_1046622_+|PQQ-binding-like-beta-propeller-repeat-protein
MDTRANRFLPIFLLLAGFGVSKATAAEPTWTQFRGADRAGIVPDAALPVQWDAKKNIRWRTELPGEGWSSPVTDGKRIYLTAAIPSDKAAAGEDASNGSFDLSLLIIDAETGELQTQQTLIHQTAEETQKIHAKNSHASPTTILDGDRLYSHFGFQGTVCTDLQGKTLWINRDLSFKAIHGNGGSPVLVDNRLVFTCDGASEPFVAALKTDTGELAWKCPRPVEAKKKFSFCTPAVIKVDSKQQIVAPGSNCVLGIDPADGSILWQVDYDGYSVIPQPVYAGGILIVCTSYDKGGLLAIDPRGRGNITETNVLWQLDKGAPKTPTPLMQSGLLYMINDAGVAYCLDAASGDRVWQKRIGGQYSASPLLADGKIYFTSEAGETTVIQASRDFQELARNDLGERTLASLAPLDSSILLRTAKALYRIETP

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Crispr_ID: NZ_CP036292_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_8

1135473-1135570

Orphan

Consensus_repeat	Method
GCTGCCGCCGCTTCGCGGCTGATGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_8

>merge|NZ_CP036292|8|1135473-1135570|CRISPRCasFinder
GCTGCCGCCGCTTCGCGGCTGATGCGCGCTCTTAAACCCTCTCGATCCGTGGGCTGATGCCCACGGCTAGATGCTGCCGCCGGCTTCGCGGCTGATGC

>NZ_CP036292|8|8|1135473-1135570|CRISPRCasFinder
GCTGCCGCCGCTTCGCGGCTGATGC	GCGCTCTTAAACCCTCTCGATCCGTGGGCTGATGCCCACGGCTAGATG
CTGCCGCCGGCTTCGCGGCTGATGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145118012.1\|1133484_1135320_+\|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl\|CDD\|176521
NZ_CP036292.1\|WP_145117996.1\|1117967_1120505_-\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|274225
NZ_CP036292.1\|WP_145124013.1\|1135641_1138347_-\|insulinase-family-protein	unknown	unknown	gnl\|CDD\|223685
NZ_CP036292.1\|WP_145118002.1\|1125691_1127167_+\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|369346
NZ_CP036292.1\|WP_145118008.1\|1130081_1130726_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225183
NZ_CP036292.1\|WP_145118000.1\|1122410_1125671_+\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377872
NZ_CP036292.1\|WP_145118004.1\|1128062_1129052_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145118010.1\|1131148_1132183_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145118022.1\|1145855_1146872_-\|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|237845
NZ_CP036292.1\|WP_145118020.1\|1145047_1145830_-\|tRNA-pseudouridine(38-40)-synthase-TruA	unknown	unknown	gnl\|CDD\|234577
NZ_CP036292.1\|WP_145118006.1\|1129059_1130085_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145118024.1\|1146929_1148114_-\|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme	unknown	unknown	gnl\|CDD\|335469
NZ_CP036292.1\|WP_145118018.1\|1143261_1144929_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|367754
NZ_CP036292.1\|WP_145117994.1\|1117386_1117803_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145117998.1\|1121073_1122132_-\|PA0069-family-radical-SAM-protein	unknown	unknown	gnl\|CDD\|275263
NZ_CP036292.1\|WP_145118014.1\|1138484_1139819_-\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|224157
NZ_CP036292.1\|WP_145118030.1\|1150621_1151206_-\|GtrA-family-protein	unknown	unknown	gnl\|CDD\|377229
NZ_CP036292.1\|WP_145118026.1\|1148275_1149115_-\|carbon-nitrogen-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|143587
NZ_CP036292.1\|WP_145118028.1\|1149282_1150359_+\|TAXI-family-TRAP-transporter-solute-binding-subunit	unknown	unknown	gnl\|CDD\|270238
NZ_CP036292.1\|WP_145118016.1\|1140326_1143098_+\|2-oxoglutarate-dehydrogenase-E1-component	unknown	unknown	gnl\|CDD\|236499

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145118012.1\|1133484_1135320_+\|glycerophosphodiester-phosphodiesterase	gnl\|CDD\|176521	cd08579, GDPD_memb_like, Glycerophosphodiester phosphodiesterase domain of uncharacterized bacterial glycerophosphodiester phosphodiesterases. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in uncharacterized bacterial glycerophosphodiester phosphodiesterases. In addition to a C-terminal GDPD domain, most members in this family have an N-terminus that functions as a membrane anchor.	9.88681e-81
NZ_CP036292.1\|WP_145117996.1\|1117967_1120505_-\|c-type-cytochrome	gnl\|CDD\|274225	TIGR02604, Piru_Ver_Nterm, putative membrane-bound dehydrogenase domain. All proteins that score above the trusted cutoff score of 45 to this model are large proteins of either Pirellula sp. 1 or Verrucomicrobium spinosum. These proteins all contain, in addition to this domain, several hundred residues of highly variable sequence, and then a well-conserved C-terminal domain (TIGR02603) that features a putative cytochrome c-type heme binding motif CXXCH. The membrane-bound L-sorbosone dehydrogenase from Acetobacter liquefaciens (Gluconacetobacter liquefaciens) (SP\|Q44091) is homologous to this domain but lacks additional sequence regions shared by members of this family and belongs to a different clade of the larger family of homologs. It and its closely related homologs are excluded from the this model by scoring between the trusted (45) and noise (18) cutoffs.	3.5239e-25
NZ_CP036292.1\|WP_145124013.1\|1135641_1138347_-\|insulinase-family-protein	gnl\|CDD\|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	4.81679e-69
NZ_CP036292.1\|WP_145118002.1\|1125691_1127167_+\|DUF1501-domain-containing-protein	gnl\|CDD\|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	1.2613e-135
NZ_CP036292.1\|WP_145118008.1\|1130081_1130726_-\|hypothetical-protein	gnl\|CDD\|225183	COG2274, SunT, ABC-type bacteriocin/lantibiotic exporters, contain an N-terminal double-glycine peptidase domain [Defense mechanisms].	5.83956e-09
NZ_CP036292.1\|WP_145118000.1\|1122410_1125671_+\|DUF1553-domain-containing-protein	gnl\|CDD\|377872	pfam07583, PSCyt2, Protein of unknown function (DUF1549). A family of paralogues in the planctomyces.	6.83014e-90
NZ_CP036292.1\|WP_145118004.1\|1128062_1129052_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	3.24146e-29
NZ_CP036292.1\|WP_145118030.1\|1150621_1151206_-\|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.	2.53771e-08
NZ_CP036292.1\|WP_145118020.1\|1145047_1145830_-\|tRNA-pseudouridine(38-40)-synthase-TruA	gnl\|CDD\|234577	PRK00021, truA, tRNA pseudouridine(38-40) synthase TruA.	1.66523e-115
NZ_CP036292.1\|WP_145118022.1\|1145855_1146872_-\|aspartate-semialdehyde-dehydrogenase	gnl\|CDD\|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	0
NZ_CP036292.1\|WP_145118024.1\|1146929_1148114_-\|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme	gnl\|CDD\|335469	pfam03781, FGE-sulfatase, Sulfatase-modifying factor enzyme 1. This domain is found in eukaryotic proteins required for post-translational sulfatase modification (SUMF1). These proteins are associated with the rare disorder multiple sulfatase deficiency (MSD). The protein product of the SUMF1 gene is FGE, formylglycine (FGly),-generating enzyme, which is a sulfatase. Sulfatases are enzymes essential for degradation and remodelling of sulfate esters, and formylglycine (FGly), the key catalytic in the active site, is unique to sulfatases. FGE is localized to the endoplasmic reticulum (ER) and interacts with and modifies the unfolded form of newly synthesized sulfatases. FGE is a single-domain monomer with a surprising paucity of secondary structure that adopts a unique fold which is stabilized by two Ca2+ ions. The effect of all mutations found in MSD patients is explained by the FGE structure, providing a molecular basis for MSD. A redox-active disulfide bond is present in the active site of FGE. An oxidized cysteine residue, possibly cysteine sulfenic acid, has been detected that may allow formulation of a structure-based mechanism for FGly formation from cysteine residues in all sulfatases. In Mycobacteria and Treponema denticola this enzyme functions as an iron(II)-dependent oxidoreductase.	4.80989e-36
NZ_CP036292.1\|WP_145118018.1\|1143261_1144929_+\|hypothetical-protein	gnl\|CDD\|367754	pfam03983, SHD1, SLA1 homology domain 1, SHD1. NPFXD peptides specifically interact with the SHD1 domain. NPFXD is a clathrin-facilitated endocytic targeting signal. NPFXD was originally discovered in the cytoplasmic domain of the furin-like protease Kex2p. Sla1 is thought to function as an endocytic adaptor.	6.76181e-11
NZ_CP036292.1\|WP_145117998.1\|1121073_1122132_-\|PA0069-family-radical-SAM-protein	gnl\|CDD\|275263	TIGR04470, hypothetical_protein_ALIPUT_00462, radical SAM mobile pair protein B. Members of this family are the downstream member (B) of a pair of tandem-encoded radical SAM enzymes. Most of these radical SAM gene pairs have an additional upstream regulatory gene in the MarR family. Examples of high sequence identity (over 96 percent) from cassettes in several Treponema species of the oral cavity to those in multiple Firmicutes in the gut microbiome suggest recent lateral gene transfer, as might be expected for antibiotic resistance genes. The function is unknown.	1.69284e-29
NZ_CP036292.1\|WP_145118014.1\|1138484_1139819_-\|MBL-fold-metallo-hydrolase	gnl\|CDD\|224157	COG1236, YSH1, Predicted exonuclease of the beta-lactamase fold involved in RNA processing [Translation, ribosomal structure and biogenesis].	2.49635e-85
NZ_CP036292.1\|WP_145118026.1\|1148275_1149115_-\|carbon-nitrogen-hydrolase-family-protein	gnl\|CDD\|143587	cd07197, nitrilase, Nitrilase superfamily, including nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes. This superfamily (also known as the C-N hydrolase superfamily) contains hydrolases that break carbon-nitrogen bonds; it includes nitrilases, cyanide dihydratases, aliphatic amidases, N-terminal amidases, beta-ureidopropionases, biotinidases, pantotheinase, N-carbamyl-D-amino acid amidohydrolases, the glutaminase domain of glutamine-dependent NAD+ synthetase, apolipoprotein N-acyltransferases, and N-carbamoylputrescine amidohydrolases, among others. These enzymes depend on a Glu-Lys-Cys catalytic triad, and work through a thiol acylenzyme intermediate. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer. These oligomers include dimers, tetramers, hexamers, octamers, tetradecamers, octadecamers, as well as variable length helical arrangements and homo-oligomeric spirals. These proteins have roles in vitamin and co-enzyme metabolism, in detoxifying small molecules, in the synthesis of signaling molecules, and in the post-translational modification of proteins. They are used industrially, as biocatalysts in the fine chemical and pharmaceutical industry, in cyanide remediation, and in the treatment of toxic effluent. This superfamily has been classified previously in the literature, based on global and structure-based sequence analysis, into thirteen different enzyme classes (referred to as 1-13). This hierarchy includes those thirteen classes and a few additional subfamilies. A putative distant relative, the plasmid-borne TraB family, has not been included in the hierarchy.	5.71413e-80
NZ_CP036292.1\|WP_145118028.1\|1149282_1150359_+\|TAXI-family-TRAP-transporter-solute-binding-subunit	gnl\|CDD\|270238	cd13520, PBP2_TAXI_TRAP, Substrate binding domain of TAXI proteins of the tripartite ATP-independent periplasmic transporters; the type 2 periplasmic binding protein fold. This group includes Thermus thermophilus GluBP (TtGluBP) of TAXI-TRAP family and closely related proteins. TRAP transporters are ubiquitous in prokaryotes, but absent from eukaryotes. They are comprised of an SBP (substrate-binding protein) of the DctP or TAXI families and two unequally sized integral membrane components. Although TtGluBP is predicted to be an L-glutamate and/or an L-glutamine-binding protein, the substrate spectrum of TAXI proteins remains to be defined. A sequence-homology search also shows that TtGluBP shares low sequence homology with putative immunogenic proteins of uncharacterized function. The substrate-binding domain of TAXI proteins belongs to the type 2 periplasmic-binding fold protein (PBP2) superfamily, whose members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. PBP2 typically comprises of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and tworeceptor cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	3.36825e-80
NZ_CP036292.1\|WP_145118016.1\|1140326_1143098_+\|2-oxoglutarate-dehydrogenase-E1-component	gnl\|CDD\|236499	PRK09404, sucA, 2-oxoglutarate dehydrogenase E1 component; Reviewed.	0

>NZ_CP036292.1|WP_145118012.1|1133484_1135320_+|glycerophosphodiester-phosphodiesterase
MFQTVCRNLYSCFRTLLAVDLIFKLAAFTLLSPAVSLLFRLFLSLSGRSVLADADIARFLLHPTGWLAVVIVGGGVLAVLALEQAVLMTVCLGADQSLKIRPSRVAIFVAERTRQVLWLTTRVVARVALTALPFLAVGGGLFLFLLTDHDINFYLTAKPPKFWLAVGLIGTVLIAMSVALLYRVSGWAFALPLLLYRGLSPTEALSESKRLASPHRWRIVGSLAIWAISNLALGFCLSFLLATLGELVLPSATRTIWTLIAAVGMLLVVFAIANFIASLIANASCASLLGMLYLRHVDEPGQRLVEMPTWSQWNGIRLTGGRIVSAVLIGGLVAAVLGVLTLESISIEDRVQITAHRGGATHSPENTMAAFRRAIEDGADWVEIDVQEASDGVVVVAHDSDLKKVAGNPVKIWNATAEELRSIDIGGYFSADYRSERMPMLEEVLALCKDTVGVNIELKYYGHTDRLEQRVVDLVERFEMEDQIVIMSLDAKGIAKLKKLRPDWTCGLLTAVAVSDLTRANVDFLAVNTSLATQSFINAAHRVGKTVSVWTVNDAKTMSAMISRGVDNLITDDPALARKVLAERETMNPVERLMLELAFQLGLPMPAGAPQ
>NZ_CP036292.1|WP_145118010.1|1131148_1132183_-|hypothetical-protein
MSIHSLFGRLAVLTIFISLSASELHAEDESLTQEVIQGLRKWRETISSLRIDYVYRNPNEVKAEHPDWSEVEVEGCYFVGRWIWKDDGSVYSRLSPYRNGKDVGNHMVEGANFRTNEIYQANFGVEEDGSQYLKSLSVKPMRSGSAITGNPMPLMRLWQSGRWFDDAIEAGQYVATNQPNTTLIQIKTLSTANPEVTLVDRQQQYLVQTIHHEAIGSKFSVEEYQSLENGTLFPNNGKYFAGNATPRDQVIEWEIVAIGINEQHDSGLFIPPETGQKTYIHDSTPARKYRRRDLPPSQVAAMADQIEMKDGPIRAIVPRGLQIQYMLLGLASICLVLGVWLARR
>NZ_CP036292.1|WP_145118008.1|1130081_1130726_-|hypothetical-protein
MRQAAKVRLLDARTRIKVQGMYRYYCTHWVLFATICFGASKSEGSGELSRQDVACGPSSLAICVSLLQERNIPMPDLRLAFDEQLNGEHTYQQVADAAQKCGLVTQFVSHDTTRLAVGKLPLIAAIRKPNGHMHFIVLFGQRDNKIQVLDSPLPARWIDKNQLITVWNGDGLYCATSVHQLMEEGVKRDFASVPLGGSLLIVFLAIYFGCKFCR
>NZ_CP036292.1|WP_145118006.1|1129059_1130085_-|hypothetical-protein
MNQSARIKHWKWIVPLPALLSLGFLCHNWYHKQQRPRFAIQYELVAPNAIDGYIEAGRDARVKLRYKLTNVGREPLRGIATDLGCTCQILKQPEDIFPNESDLLEFSLRAPSAGAIQRKIPILIESQRQPLVFIQVALRVPVLTPSFLHQQRELNISFIDGDSLGRRITVETIERADSDTWIAKLETTPPSLVNFTEPTVHERPNRDPALTHRTYLFEASAGQEIDSAHAGVYVLRDRSGAPLHKPQLIRVKRLPRFTNHPSSPVVRTGENTKILVLDRLGRSSLTVFRYDQELIAVTPGAVKNTFLVSLRKSTIDTKMTELELRSEDGSKVHIPLCFACD
>NZ_CP036292.1|WP_145118004.1|1128062_1129052_-|DUF1559-domain-containing-protein
MCRCKFRNAFSIIELLVVIGVAAIALAVALPAAQHTRAKARRIQCALRLSELSIATNIHLSTYNTFPYTSKNFGVFVNGSAKRFPAISPHSQLLASLDQAAFEKVAIFDPSLSWTDRQPISTVESNRILIKTSMPMFLCPSDSGPVGGNNYRANLGPDIGVFRGSPPTTHNGIGAFENGRALSPSSFSDGLSNTIMYSEKVIGDRNRTVYQAFRDNFVFSPGFTNRDEAARTCRQFATSTPLSHDSFGGTTWLFGGYNHTWYNHVATPNSFIPDCCTGLSFGGGDGLYTARSLHHGGVNVGMADGSTNFISNSIDALVWLQQSTRSSGD
>NZ_CP036292.1|WP_145118002.1|1125691_1127167_+|DUF1501-domain-containing-protein
MTLKTQNAACGRTERRQFLSDFGLGFTGLALGAMMHRDAQGSTAEAALRGLPHFAPRAKSVIWFFMNGGTSHLESFDPKPALNQHAGKTIDESPLGQAIVDSPFYRKNVVDFGGKPRAMMSQIYPMQVGYGPRGESGIEVSDWWPHVGDCIDDIALVRSMWTTDNDHAAQLQFHTGRHIFDGFFPSIGSWVHYGLGSLNDNLPQFVVMGQPPGDCCGGVGAHDGSYLGPQHAGVQMASDPKRPLAFGTPGAGTRISQQRDQLNLLDDLHRMTAAARPDDEALQARIKAYELAFRMQMSVPEIVDLNRETKQTQAMYGLDVKETQQVGRHALTARRLVEQGVRFVQIYDGGGGGGGWDAHTKLKENHARNSARVDKPIAGLLKDLKQRGLLEETLVVWATEFGRTPGAEKSDGRDHHPYGFSVWMAGGGLKGGIAHGATDELGFHAVEARHYVTDIHATVLHQLGLDPRQLSLPSQKRLEIDYGNPIEAIIA
>NZ_CP036292.1|WP_145118000.1|1122410_1125671_+|DUF1553-domain-containing-protein
MSTLSTRFLLCCIVPFAAAFSERPACAVDYLTDIKPLLEEKCYACHGPLKAQGDLRLDTAVALIAGGGSGAAIKRGDPGESFLIDVLTGEAGYQMPPENEGAVMTPAQIDLFRQWIADGAPSPADEEPAADPKTWWSYQAITRPPLPEVNAPNWPLGPIDHFVAARRQANGLPHAPPADRATWLRRVYLDLIGLPPTVEQQQAFLNDDSPMAFEAVVDELLSRPEYGQRWGRHWMDVWRYSDWYGSRGSNEIRYSQRHIWRWRDWIVDSLNDNKGYAAMVREMLSGDERIDPADPTSLVATGYLGRSWYKFDRDVWLFETVERTGEAFLGLTLRCCRCHDHKFDPVSHEEYFRFRSFFEPHDVRTDPISVLTEMQKDASQGMVPTDGIPLVYDKTADTPTYRFERGDSRFPDKSKPLEPGVPESLGGSVDLQPIDLPALAWYPMLRPGVRETLIEKAVSEAEIAAVALADAQAALREMQDKPAAESLAEKADGVGDMVLLHDNFDAPNPKLWLRQSGNWKVEEGSLWQTDVGSFATIVADRMLPLDFKFRLRYRTLAAGSFRSVGLSFDYQDAGNSQDVYTSVNDSQPSVQAFHREGGQQAYPTEGIVYTPLKVGDEIVLDVTVAGSQLTIDMNGTRKLDCQMPIARRSGKLALWVHQGAAEFLELEVTRLPPSAETLALQQREAKHAVDLARLKHQAAQAHVESTRLRIAAEVKRYLDPQSAEEPEDLDRWLTAAAEAEARLRVCEAEVEFFEAVPSAEKLEAAKSKLAAAEAKLNDPANRDYEPLGPKFPRTSTGRRSALADWIVDPQNPRTARVAANHLWGRHFGQPLVATTENFGLNGRKPSHPQLLDWLADELVRNDWKMKPLHRQIVLSATYRMSSDPLPVGNDAALQIDPENRLLWRMNPRRMEAELVRDSTLFLASQIDLSFGGPEIPVEQGDESRRRSLYLRNTPNEKVPMLEVFDVADPNACYRRQESIVPHQSLAMMNSGLAIDAARTIARRLADASDFVDVAFETILARRPTAAEADRCDAFLQSHAELLQQASGEKFPGADTATTPRAADPIQAARENLIHVLMLHNDFVTIR
>NZ_CP036292.1|WP_145117998.1|1121073_1122132_-|PA0069-family-radical-SAM-protein
MRHGSELDPPNRFESIRRELDLEQLQWDQEHLASHDRREIEYLPDDSKSIVSENKSPDIPFRYSVNPYRGCVHGCSYCYARNTHEFLGFNAGLDFETKIMVKHKAPQLLETFLNRKSYQPETISFSGVTDCYQPAERQFRLTRQCLEVALRYQQPVGIVSKNALVVRDLDLLQLLAAQNLVHVYLSITTLQPELARAMEPRTSIPTARLRAVRMLAEAGVPVGVMVAPVIPGLNDSEIPAILDQARQAGAATANFILLRLPLTVEPVFREWLQRTQPEKQELIEARVRQTRDGSMYDSQWNQRMRGSGPIAEQIKQMFQLFAKKHGLDKPLPQVDSSRFQNPNAGPQQMNLF
>NZ_CP036292.1|WP_145117996.1|1117967_1120505_-|c-type-cytochrome
MKTRRLVFEHLSRIHGVARATCLLLMISCVGASAYGDDDLPGGGQATPVDSIALPAGFRAQLLRSAETGEGSWVSMTFDDRGRVILGRDKRGVVRLTLSDDRGQVDQFEVIENTLKHCRGILWAHDSLYVCATNNSGFYRLRDTNGDDQFDSVQELMPFDYQSRYGHGPNQIVLGPDNMLYVVNGNDVAFPEGFAADSPYRDPEDDHLLPEPRDTVEDIRVGYVAKTDPEGKNWEIVAGGFRNQFDVAFNAAGEMFTYDADMEWDVGLPWYRPTRLNHVVSGGEYGWRWGTGKWPDYFADSLPTTLDTGLGSPTGLEFGTRSQFPPEYRESLFMGDWQHGRIFQVELTPRGASYGGQYKVFLEGGALNVCDLTFGPDGAMYFITGGRGSQSGLYRVTYEGPEVAAPSLDAEQTDQAQASAAARQVRHQLEQWHTRSDADAKAIDFIWPHLNSDDRWLRFAARLAIERQDLELWRERALNESQPKASIAALLALAHRGRAEDQSQLLTALGRLPLATLGREDLLDALRVWQLSFIRQGEPSESDRTESLSQLSPLYPQTSGYVNRELCSLLIYLQAPDVVPRTVELIRTAIGQEDMIYYSQRLARLSEGWTNETREAFFDSLLAARRFQGGKLLSASLQNIQEDAIATLTEAEKEHLKPRLEMLATAVDGSSEHESPSASFVKQWTWEELEAELPRARHGRSWEQGRTALAKAQCVKCHRVSEQGSSTGPDLTHVGSRFDERALLESIVQPSKVIDEKYRLSSYLLDSGELVTGRPIGVSATMITVQTDSMRAETVPLKRAEIEQTTPSGLSPMPSGLMNVLTLDEILDLIAYLRSSGDPQADAFQ
>NZ_CP036292.1|WP_145117994.1|1117386_1117803_+|hypothetical-protein
MNLFDLFPNLTADNHEVTSQKTIKYNCIAWAARNVDRWWQPGVFWPIQSSREDIGIGNLVAAFKALGYEECDDGTLDDGFEKLAIYGSGLMYTHAARQLPDGRWTSKLGQLEDITHWTTEAIEGGDYGEVVQFMKRPT
>NZ_CP036292.1|WP_145124013.1|1135641_1138347_-|insulinase-family-protein
MGLVALTAICAPHTFGEGPMKVTEIEGISEYELDNGCKILLFPDPSKPVVTVNVTIFVGSRHEGYGEAGMAHLLEHMLFKGTPSHPEIPKLLQDHGARFNGTTWTDRTNYYETLPASDENLEFALRLEADRLVNSTIKGEDLASEMSVVRSEFESGENDPSRILMQRMQSAAYEWHNYGKSTIGNRSDIERVPVVNLRRFYKKYYRPDNVLVTVAGQFDPEKALEYLQKYFGSLETPDTPIDRTYTVEPPQDGERTVVLRRVGDVQWVGAAYHIPAGSHEEYAAAKVLSYVLGDEPSGRLYKSLVETEKASNVYAFGFGFHDPGLTLALAEVPKDKDIEVARQQLLLTMEHGFEEKPVTEEEVERARQQLLKSRELEAADSDRLAVSLSNWAAQGDWRLYFLFRDRLEALTAADVQAVAEKYLTRNNRTTGLFIPTDEAQRITIPEAPDLNALLADYKGRESIQAGEAFDTSPLAIDQRTERGQLTDTVEYSFLPKKTRGASVNLMLTLRYGTPESLQPRVIAADVLPQLMARGTESLDYQQYQDKVGKLRAQISLSGTTGLLQVSVKTNREQLPEVLELLTEVIRKPRLDAEELDVLKRQTITGLESQLSEPQALAPISTRRALSPYPKTDVRYRPTIEEEIAMYKDLKIDQVRELYNDFVSSQSTELAVVGDFDPELIKSKLKPALEGWKSDHPYVRIDRPAHPDLPGEVKTINTPDKANAVYYAGQQYVMSDTDPDYAAMVMGNYVLGAGALSSRLGDRVRQQEGLSYGIRSGFSVSTKDDRGEFTIFAITNPNNKDKLMTVIREEIDKILADGITDEELAKAKEGYLQRESVRRSDDSYIASQLVLNMFTDRTMAFTDQQEKKIAAVTKDQVNAALKKYIDPERLIISVAGDFKAKE
>NZ_CP036292.1|WP_145118014.1|1138484_1139819_-|MBL-fold-metallo-hydrolase
MKLIHHGGHLGVTGSCHQLWTDDEHSLLVDCGTFQGDDARDHPNPEIKFSLRGIESLLLTHVHIDHCGRIPHLIAAGFEQPIYCSGPTARLLPLVMQDALKIGFTRNQRLIDKFNDKIAKLLQPLPYHQWHPIQGGCKLRLRPAGHVLGSTIFEVELPNGQMAVFSGDLGPRHAPLLTEFSSPERADLLVMESTYGNRIHEGRADRQSRLEAVLRKTLDDKGVTIIPAFSLGRTQDILFEMNGIFEAIQKQQGRSLMKQVDVIVDSPLASRFTQIYDDLQEFWSAEAQGVLKTDDQPLVFENLTTVGDHQEHLATLDQLVKHKLPAVVVAGSGMCTGGRVMNYLRRLIGEPTTDIVFCGYQARGTPGSYIQRGSDWVRLDGRKYQIRADVHQLSGYSAHADQRDLLRFVAGFTEKPYQIRLVHGEYHVRKALEAELDQRGYHVD
>NZ_CP036292.1|WP_145118016.1|1140326_1143098_+|2-oxoglutarate-dehydrogenase-E1-component
MNTYSLGYIDDLYVQYVKDPESVSPGWRRYFEQFLVATDETTAKLTEAATAAADGDGQTLGNVTEHALWLARMQDQVDQLVREYRVRGHLVAQVDPLGMAQKGCPELNVESYGLTEDDLSRPFDSSALENVQGRTLNDVLQQLRNTYCRNIGAQFMHIDNRNIRDWLQRRMEVGENRMPLSHEVQRRIYSRLADATIFEEFVRRKFVGAKTFSLEGAESLIPLLDLALEKCGQHNVKEVVMAMAHRGRLNVLANIFKKRALNIFWSFDDPDPQLHRGGGDVRYHLGYSSDWKTASGDKMHISLCFNPSHLEYVNPVALGRTRCKQDRYGDSKRQDVVTILIHGDAAFAGEGVVQETLNLSQLKAYHTGGTLHVVINNQVGFTTEPREGRSTTYATDIAKMLQIPIFHVNGEDPEAVAQVVNLAMDFRREFHSDVVIDMYAYRRWGHNEGDEPRFTQPEMYREIDARQSVRKSYRKRLLKLGQMTDEEAKELHRKRQDKLEREFEATRTVPFVPDVQSLGGSWSEYVGGPEPENDTVVTGVDKKRLSELLETLTTIPQEFNLHRKLKRPYEQRREMAAGKLPVDWATGEALAFATLLTEGRRIRLTGQDSERGTFSQRHAVLHDEESGSIYTPLEHLAPDQAKFEIANSPLSEAGVLGFEYGYSLDCPEGLCAWEAQFGDFWNCAQVIVDQFIASAEDKWNRLSGLVMLLPHGFEGQGPEHCSSRVERFLAMAAEHNIQICQPTTPAQYFHLLRRQVLRRWRKPLICLTPKSLLRHPLVVSDLKDLEARQFRKILPDTQVSPDNARRILLCTGKVYYDLLEARKQRGLEDVAILRIEQLYPLKQHELMSSFGGYAEGKDIYWVQEEPKNMGAWPYLKLNYGDQLAERFKLHCVSRVESASPSTGSMRTHKLEQEELLEAAFASL
>NZ_CP036292.1|WP_145118018.1|1143261_1144929_+|hypothetical-protein
MLLKISIALLGCAAIAAASVPGRLLAEPLRYAPESGSRFAYRFEIVVDGDDETITYKGVTKYTVNAVKEDRVRLTYHGGLSESKKAKGRQGRGGRRFGPPSIPRPFSRPAFAGKVTTTNQITLSPQGEVLAMNGDSQLPYLLGNVSLMPFETLPEEETQAWTIDSGVSITKNEQNGRMGGRFGPLDPFGRGDNGPKDVRAAGEVTKYSITGEQDGRVQISKSYQLTMPANDKNQTYEMTGSGSWTFDRTAALPDAIDIQYKLVVNDGNTTVTVPIHVKYDRISGEELDRMEAEAKRIAEERAMAAKQAKEEAERPLSEEELAAAIADLQSGDDGKIQAQLEALAKKSVADPSPKVAAAIEAHIEHEDKKLRSAAHNALMRWAPDYKVVQDLKKAYGGFGTVKSTDREVDALTPLYVGQIVQFQEHGSFWFPGEIVSLNADKSVVVRRRAGSSRKVTVKRRNVQLAPEQLPQPNKPASVSAAPMAAEGTSPVRTWSDATGRFKIEANLLRVENGGAVLKRTDGREVTVPVTKLSAADQTYLKAWEAALNADNPFEP
>NZ_CP036292.1|WP_145118020.1|1145047_1145830_-|tRNA-pseudouridine(38-40)-synthase-TruA
MLRTFRLTIGYDGFRYAGWQVQADLPTIQGELQRAFAELTGERVSITGSGRTDSGVHAIAQVASLTTDAWRSSDAALGRAINTKIPDDITVYRCEEMPVDFHALRDAVGKRYRYQLQIGGVRDAFDFRYFWHHHVQLDIEAMQQAAAMIVGTHDFACFQATGSERKTTVRTIHDLALTTGQGRAGQGHLIVEVEANGFLYNMVRNIVGSLVEVGRGKHPPAWIEELIAGRDRNQAGPTAPAHALFLLRVDYDVQPLAAQQ
>NZ_CP036292.1|WP_145118022.1|1145855_1146872_-|aspartate-semialdehyde-dehydrogenase
MIDTLAVVGATGAVGRIVLDQILQRKLPHGRLRLLASARSAGQVVTFGDQQITVELMEPSAFDGVDVVIASTPDEVSAEFAPWAVERGAIVVDESGYWRMDPKVPLIIPEVNASAIDNHQGIIASPNCSTTQMVVALAPLHNAARIKRVVVSTYQATSGAGLAGEAELMHSTRGSLDGSAPAAKTFQYPIAFNLIPQIGSEKHEGYTSEEMKMVYETRKIFGDDSIDVCPTCVRVPVAIGHSESILVETEKPLTVEQARELFANADGVTLIDDLAGRQYPMPVDSAGKDDVFVGRVRKDLSSPNGIAFWCVSDNLRKGAATNAVQIAELLAKKMASVA
>NZ_CP036292.1|WP_145118024.1|1146929_1148114_-|SUMF1/EgtB/PvdO-family-nonheme-iron-enzyme
MNLYARSLSLCLFALTSCVAIAADDSAKIKGFSTTQPEKGPFVAVEGGFMVPYTETIPGTEISFEMIPVPAGSYKMGSPASEKGHKEDESPQIMVNVDPMWVCKTEVRWIEYKEFMGMYKTFKEFVFRDMRKVTPENKVDAVTTPTELYEPSYTFEFGDDDDLPAVTMTQFAAKQFTKWLSKMTDTQYRIPTEAEWEWAARAGSTTAYSWGESADEIDQYAWYADNSPDGPSKVGLKKPNAFGLNDMLGNVAEWTIDAYLEDGYKVFEGKTVKASEAIKSIETADPRVVRGGSWEMEPEDVRCASRLYSVDEDWKMDDPNIPLSPWWFTSDPSRGVGMRLFRSWKPLSDEAMNKFWEIDSEDIEFDVMSRIEEGRGVLGLADPDLAEAAKAVRE
>NZ_CP036292.1|WP_145118026.1|1148275_1149115_-|carbon-nitrogen-hydrolase-family-protein
MSQQTKRVAAVQMDVAFADIDHNVQQILAKIATVKADGVDLAVFPECALTGYCFESREEALPLGLSIDDPLFDSFAAACGDSDLHVIIGFLEIEGDKLFNSQAMINRSGVVGSYRKIHLPGVGVDRFLDSGDREFSIQAAGEIRVGMAICYDSSFPETARVLGLHGADVIALSTNWPVAARRTAEIVPPARSMENHLYFIAANRVGTERTFEFCGMSSIAGPDGVMIAETDSDQELILTADIDLSIARNKQIVRTPGKHVIDRFADRQPERYTIIGEKK
>NZ_CP036292.1|WP_145118028.1|1149282_1150359_+|TAXI-family-TRAP-transporter-solute-binding-subunit
MALMLQISQHRALVASLVLSALMLGCKKSDSTGDGGATGGRQFLSMGTAPVGGAFPVVGGAIAEVLNEHKGTVDWKVQAKGTKGSQENIRRLQQAELELALSNAAISYFAARGEAGWDKVYDIRAIATLAPNVALFIARADSGIQSIADLKGKRVITGPAGAGFQQFVEPILAEHGVAWDEITSLNATQSGAVDQLGDGAADAAFLGGAVPTGSITQAASTFDVTYIPFDESARQKLIEKYAFFHPATIPGGTYKGLDNDFLGLNVGSMHLITAASQSDELIYEVTKSIWENRAEIAGKHPAGKAINEKNVARNTGIEYHPGAIKFYEEVGVLEAAEKPAAEEAPAADAPAEAPAAAE
>NZ_CP036292.1|WP_145118030.1|1150621_1151206_-|GtrA-family-protein
MADRSCIADRLRPGSWNRSDRRTAADTADLERDRRRTNADRSTIDASEFADSFGMIRASVSAPRASRAIRFLILSGVSFLGNLGITHALTQHAAWPAELAFAASLVIIFFVNFACCRWFVFQANEQPIATQLASFLTATICFRGLEYAAFLGLHSLLGIHYLIATATVLIAGFAAKFLFYNRFVFGRPNTATQP

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Crispr_ID: NZ_CP036292_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_9

1464613-1464716

Orphan

Consensus_repeat	Method
GATGGTCGCCTTTCGCTCCGCGAAAGT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_9

>merge|NZ_CP036292|9|1464613-1464716|CRISPRCasFinder
GATGGTCGCCTTTCGCTCCGCGAAAGTGCGGATCCCGAATTCGCGCTCCGCGAACCGGACGCTAACGCGTGGCGGCTGATGGCCGCCTTTCGCTCCGCGAAAGT

>NZ_CP036292|9|9|1464613-1464716|CRISPRCasFinder
GATGGTCGCCTTTCGCTCCGCGAAAGT	GCGGATCCCGAATTCGCGCTCCGCGAACCGGACGCTAACGCGTGGCGGCT
GATGGCCGCCTTTCGCTCCGCGAAAGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145118438.1\|1472598_1473912_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145118430.1\|1467781_1469374_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145118442.1\|1474645_1476079_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224154
NZ_CP036292.1\|WP_145118432.1\|1469351_1469999_-\|SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|223813
NZ_CP036292.1\|WP_145118436.1\|1471521_1472559_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270236
NZ_CP036292.1\|WP_145118434.1\|1470102_1471500_+\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|238194
NZ_CP036292.1\|WP_145118426.1\|1464921_1466892_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|273429
NZ_CP036292.1\|WP_145118414.1\|1453381_1454845_+\|protoporphyrinogen-oxidase	unknown	unknown	gnl\|CDD\|237009
NZ_CP036292.1\|WP_145118418.1\|1458633_1459674_-\|transporter	unknown	unknown	gnl\|CDD\|379259
NZ_CP036292.1\|WP_145124034.1\|1447400_1448654_-\|prolyl-oligopeptidase-family-serine-peptidase	unknown	unknown	gnl\|CDD\|225989
NZ_CP036292.1\|WP_145118422.1\|1460984_1461824_-\|purine-nucleoside-phosphorylase	unknown	unknown	gnl\|CDD\|350160
NZ_CP036292.1\|WP_145118424.1\|1462175_1464602_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|223510
NZ_CP036292.1\|WP_145124033.1\|1446094_1447387_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|225743
NZ_CP036292.1\|WP_145118416.1\|1455176_1458200_+\|DUF5117-domain-containing-protein	unknown	unknown	gnl\|CDD\|379818
NZ_CP036292.1\|WP_145124035.1\|1450669_1453369_+\|DNA-gyrase-subunit-A	unknown	unknown	gnl\|CDD\|235502
NZ_CP036292.1\|WP_145118428.1\|1466910_1467675_+\|hisA/hisF-family-protein	unknown	unknown	gnl\|CDD\|240074
NZ_CP036292.1\|WP_145118440.1\|1473908_1474625_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145118412.1\|1448909_1450253_+\|general-secretion-pathway-protein-GspE	unknown	unknown	gnl\|CDD\|225363
NZ_CP036292.1\|WP_145118444.1\|1476142_1477600_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|211614
NZ_CP036292.1\|WP_145118420.1\|1459928_1460792_-\|purine-nucleoside-phosphorylase	unknown	unknown	gnl\|CDD\|350160

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145118442.1\|1474645_1476079_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|224154	COG1233, COG1233, Phytoene dehydrogenase and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	9.98894e-34
NZ_CP036292.1\|WP_145118432.1\|1469351_1469999_-\|SAM-dependent-methyltransferase	gnl\|CDD\|223813	COG0742, COG0742, N6-adenine-specific methylase [DNA replication, recombination, and repair].	2.87369e-35
NZ_CP036292.1\|WP_145118436.1\|1471521_1472559_-\|extracellular-solute-binding-protein	gnl\|CDD\|270236	cd13518, PBP2_Fe3_thiamine_like, Substrate binding domain of iron and thiamine transporters-like, a member of the type 2 periplasmic binding fold superfamily. The periplasmic iron binding protein plays an essential role in the iron uptake pathway of Gram-negative pathogenic bacteria from the Pasteurellaceae and Neisseriaceae families and is critical for survival of these pathogens within the host. On the other hand, thiamin is an essential cofactor in all living systems. Thiamin diphosphate (ThDP)-dependent enzymes play an important role in carbohydrate and branched-chain amino acid metabolism. Most prokaryotes, plants, and fungi can synthesize thiamin, but it is not synthesized in vertebrates. These periplasmic domains have high affinities for their respective substrates and serve as the primary receptor for transport. After binding iron and thiamine 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 iron- and thiamine-binding proteins belong to the PBPI2 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.	5.02895e-79
NZ_CP036292.1\|WP_145118434.1\|1470102_1471500_+\|peptidylprolyl-isomerase	gnl\|CDD\|238194	cd00317, cyclophilin, cyclophilin: cyclophilin-type peptidylprolyl cis- trans isomerases. This family contains eukaryotic, bacterial and archeal proteins which exhibit a peptidylprolyl cis- trans isomerases activity (PPIase, Rotamase) and in addition bind the immunosuppressive drug cyclosporin (CsA). Immunosuppression in vertebrates is believed to be the result of the cyclophilin A-cyclosporin protein drug complex binding to and inhibiting the protein-phosphatase calcineurin. PPIase is an enzyme which accelerates protein folding by catalyzing the cis-trans isomerization of the peptide bonds preceding proline residues. Cyclophilins are a diverse family in terms of function and have been implicated in protein folding processes which depend on catalytic /chaperone-like activities. This group contains human cyclophilin 40, a co-chaperone of the hsp90 chaperone system; human cyclophilin A, a chaperone in the HIV-1 infectious process and; human cyclophilin H, a component of the U4/U6 snRNP, whose isomerization or chaperoning activities may play a role in RNA splicing. .	3.9346e-29
NZ_CP036292.1\|WP_145118426.1\|1464921_1466892_+\|AAA-family-ATPase	gnl\|CDD\|273429	TIGR01073, ATP-dependent_DNA_helicase_PcrA, ATP-dependent DNA helicase PcrA. Designed to identify pcrA members of the uvrD/rep subfamily. [DNA metabolism, DNA replication, recombination, and repair].	0
NZ_CP036292.1\|WP_145118414.1\|1453381_1454845_+\|protoporphyrinogen-oxidase	gnl\|CDD\|237009	PRK11883, PRK11883, protoporphyrinogen oxidase; Reviewed.	6.96663e-119
NZ_CP036292.1\|WP_145118418.1\|1458633_1459674_-\|transporter	gnl\|CDD\|379259	pfam13557, Phenol_MetA_deg, Putative MetA-pathway of phenol degradation.	0.000405959
NZ_CP036292.1\|WP_145124034.1\|1447400_1448654_-\|prolyl-oligopeptidase-family-serine-peptidase	gnl\|CDD\|225989	COG3458, COG3458, Acetyl esterase (deacetylase) [Secondary metabolites biosynthesis, transport, and catabolism].	1.32408e-11
NZ_CP036292.1\|WP_145118422.1\|1460984_1461824_-\|purine-nucleoside-phosphorylase	gnl\|CDD\|350160	cd09009, PNP-EcPNPII_like, purine nucleoside phosphorylases similar to human PNP and Escherichia coli PNP-II (XapA). Human PNP catalyzes the reversible phosphorolysis of the purine nucleosides and deoxynucleosides inosine, guanosine, deoxyinosine, and deoxyguanosine. Patients with PNP deficiency typically present with severe immunodeficiency, neurological dysfunction, and autoimmunity. Escherichia coli PNPII, product of the xapA/pndA gene, catalyzes the phosphorolysis of xanthosine, inosine and guanosine with equal efficiency and has been referred to as xanthosine phosphorylase and inosine-guanosine phosphorylase. E. coli PNPII is also capable of converting nicotinamide to nicotinamide riboside, and may be involved in the NAD+ salvage pathway. It is one of two purine nucleoside phosphorylases found in E. coli, which also contains PNPI, which displays a different substrate specificity and belongs to a different subgroup of the nucleoside phosphorylase-I (NP-I) family than PNPII. NP-I family members accept a range of purine nucleosides as well as the pyrimidine nucleoside uridine. The NP-1 family includes phosphorolytic nucleosidases, such as purine nucleoside phosphorylase (PNPs, EC. 2.4.2.1), uridine phosphorylase (UP, EC 2.4.2.3), and 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP, EC 2.4.2.28), and hydrolytic nucleosidases, such as AMP nucleosidase (AMN, EC 3.2.2.4), and 5'-methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase (MTAN, EC 3.2.2.16). The NP-I family is distinct from nucleoside phosphorylase-II, which belongs to a different structural family.	1.17624e-157
NZ_CP036292.1\|WP_145118424.1\|1462175_1464602_+\|ATP-binding-protein	gnl\|CDD\|223510	COG0433, COG0433, HerA helicase [Replication, recombination, and repair].	3.77726e-10
NZ_CP036292.1\|WP_145124033.1\|1446094_1447387_+\|MFS-transporter	gnl\|CDD\|225743	COG3202, COG3202, ATP/ADP translocase [Energy production and conversion].	2.72987e-35
NZ_CP036292.1\|WP_145118416.1\|1455176_1458200_+\|DUF5117-domain-containing-protein	gnl\|CDD\|379818	pfam16313, DUF4953, Met-zincin. This is a family of uncharacterized proteins that carry the highly characteristic met-zincin mmotif HExxHxxGxxH, the extended zinc-binding domain of metallopeptidases.	1.51333e-74
NZ_CP036292.1\|WP_145124035.1\|1450669_1453369_+\|DNA-gyrase-subunit-A	gnl\|CDD\|235502	PRK05560, PRK05560, DNA gyrase subunit A; Validated.	0
NZ_CP036292.1\|WP_145118428.1\|1466910_1467675_+\|hisA/hisF-family-protein	gnl\|CDD\|240074	cd04723, HisA_HisF, Phosphoribosylformimino-5-aminoimidazole carboxamide ribonucleotide (ProFAR) isomerase (HisA) and the cyclase subunit of imidazoleglycerol phosphate synthase (HisF). The ProFAR isomerase catalyzes the fourth step in histidine biosynthesis, an isomerisation of the aminoaldose moiety of ProFAR to the aminoketose of PRFAR (N-(5'-phospho-D-1'-ribulosylformimino)-5-amino-1-(5''-phospho-ribosyl)-4-imidazolecarboxamide). In bacteria and archaea, ProFAR isomerase is encoded by the HisA gene. The Imidazole glycerol phosphate synthase (IGPS) catalyzes the fifth step of histidine biosynthesis, the formation of the imidazole ring. IGPS converts N1-(5'-phosphoribulosyl)-formimino-5-aminoimidazole-4-carboxamide ribonucleotide (PRFAR) to imidazole glycerol phosphate (ImGP) and 5'-(5-aminoimidazole-4-carboxamide) ribonucleotide (AICAR). This conversion involves two tightly coupled reactions in distinct active sites of IGPS. The two catalytic domains can be fused, like in fungi and plants, or peformed by a heterodimer (HisH-glutaminase and HisF-cyclase), like in bacteria.	4.27545e-39
NZ_CP036292.1\|WP_145118412.1\|1448909_1450253_+\|general-secretion-pathway-protein-GspE	gnl\|CDD\|225363	COG2804, PulE, Type II secretory pathway, ATPase PulE/Tfp pilus assembly pathway, ATPase PilB [Cell motility and secretion / Intracellular trafficking and secretion].	4.94462e-35
NZ_CP036292.1\|WP_145118444.1\|1476142_1477600_-\|MFS-transporter	gnl\|CDD\|211614	TIGR00885, L-fucose-proton_symporter, L-fucose:H+ symporter permease. This family describes the L-fucose permease in bacteria. L-fucose(6-deoxy-L-galactose) is a monosaccharide found in glycoproteins and cell wall polysaccharides. L-fucose is used in bacteria through an inducible pathway mediated by atleast four enzymes: a permease, isomerase, kinase and an aldolase which are encoded by fucP, fucI, fucK, fucA respectively. The fuc genes belong to a regulon comprising of four linked operons: fucO, fucA, fucPIK and fucR. The positive regulator is encoded by fucR, whose protein responds to fuculose-1-phosphate, which acts as an effector. [Transport and binding proteins, Carbohydrates, organic alcohols, and acids].	2.08018e-140
NZ_CP036292.1\|WP_145118420.1\|1459928_1460792_-\|purine-nucleoside-phosphorylase	gnl\|CDD\|350160	cd09009, PNP-EcPNPII_like, purine nucleoside phosphorylases similar to human PNP and Escherichia coli PNP-II (XapA). Human PNP catalyzes the reversible phosphorolysis of the purine nucleosides and deoxynucleosides inosine, guanosine, deoxyinosine, and deoxyguanosine. Patients with PNP deficiency typically present with severe immunodeficiency, neurological dysfunction, and autoimmunity. Escherichia coli PNPII, product of the xapA/pndA gene, catalyzes the phosphorolysis of xanthosine, inosine and guanosine with equal efficiency and has been referred to as xanthosine phosphorylase and inosine-guanosine phosphorylase. E. coli PNPII is also capable of converting nicotinamide to nicotinamide riboside, and may be involved in the NAD+ salvage pathway. It is one of two purine nucleoside phosphorylases found in E. coli, which also contains PNPI, which displays a different substrate specificity and belongs to a different subgroup of the nucleoside phosphorylase-I (NP-I) family than PNPII. NP-I family members accept a range of purine nucleosides as well as the pyrimidine nucleoside uridine. The NP-1 family includes phosphorolytic nucleosidases, such as purine nucleoside phosphorylase (PNPs, EC. 2.4.2.1), uridine phosphorylase (UP, EC 2.4.2.3), and 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP, EC 2.4.2.28), and hydrolytic nucleosidases, such as AMP nucleosidase (AMN, EC 3.2.2.4), and 5'-methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase (MTAN, EC 3.2.2.16). The NP-I family is distinct from nucleoside phosphorylase-II, which belongs to a different structural family.	6.42996e-127

>NZ_CP036292.1|WP_145118424.1|1462175_1464602_+|ATP-binding-protein
MIPSVDQFEKLGAFYLGREYDLKAGRNRDDLLMYDAKDLCTHALCVGMTGSGKTGLCLSLLEEAAIDGIPALCVDPKGDLANLLLTFPDFNPEDYKPWLEQGEASRKGITLDELAASKAKLWQDGLASWGQDGERIRRFQDSVDIAVYTPGSNIGLPLTILKSFNAPPPEILEDSEAMSDRIASAASGLLALVGVDADPLSSPDHILLSKILDTNWRAGKNVTIGDLIGMIASPPFDRVGVINLDAFMSPADRTKLSMRLNNLLASPAFSTWLEGEALDIQRLMYTDEGKPRLTILSIAHLSDTERMFFVTILLNELVAWMRTQSGTSSLRAMFYMDEVFGYFPPVAKPPSKAPMLTLLKQARAFGLGVTLATQNPVDLDYKGLSNIGTWFLGRLQTERDKQRVLEGLEGAAAQTGVPFDRQEMEQTLAGLGSRVFLMNNVHDDGPRVFQSRWALSFLSGPLARDQISRLMKDRREQAAKALAESGEPAESIAAGSAQGSRPMVPAGIEERFVCPTQTPAESASLVYRPAILGKGSLHFVRSRGSIDLWQDQMRIVSCAAGVPDPLWIDSKPAPQDLQLSDRPDERYTFADLPTELVNEKSYKRWADDLKDYFYRHQTLAVYECDEVDQLAPPGSTEVQARLHFKQAAREARDRETEKLRDKFSSKMQSLEKKIRTAEDRVSREASQAQGATWQSMIQIGSTLLNGFMGNKISRRASTAANGWNRAARQKEDVHRAEAALQALHGDMADLEEDLKREIDELAERFHIENLKLEETLINPRKGDLRVDSPVLLWTPWQVDSVGIAQRLF
>NZ_CP036292.1|WP_145118422.1|1460984_1461824_-|purine-nucleoside-phosphorylase
MHDLYDKIQESTAAIKAAWGTTPRAGIILGTGLGGLVDEIEIEASLDYSEIPHFPTSTATSHRGRLVCGKLQGVPVVAMEGRFHMYEGYPLKQITLPVRVMKALGAELLVVSNACGGLNPYFQSGDIMVIEDQINLMGDNPLIGINDDRLGPRFPDMCEPYSQRLVDTALEIARRENIRAHKGVFVAVAGPNLETRAEYRFLRTIGADVVGMSTVPEVIVAVHCGLKVVGFSVITDMCLPDALQPAVVEEIIAIANAAEPNLRTLVRQSVADFANDRLA
>NZ_CP036292.1|WP_145118420.1|1459928_1460792_-|purine-nucleoside-phosphorylase
MTKHPNQQCPAERVLRTAEFIACKLAELPRVAIILGSGLGNLADYIEDAIAIDYSDIPNWGQSWIAGHSGQLIFGWLDSQPVIAMSGRFHRYEGWTTEQVSFPVRVLAAIGSHTLIVSNAAGGLNPKYRVGDIVVIRDHIDMLHGHPGQRFDYGIYPPQTRSDAPLRGASPYDQALSEKALETARLNGFPAHSGTYLATLGPSYETRAEYRFMRKIGADVVGMSTVPEVLQAQRIGMRVLGMSMVSNIARPDAPQRTDHADVLAAAQIAEPRMRAIVREAVQRSTTS
>NZ_CP036292.1|WP_145118418.1|1458633_1459674_-|transporter
MKRLNVAFLMLLAAANVSSAHDEYRSRADKHAPAGLMGDHLHAPGEWMVEYKYMNMYMDGNRAGTQRLSDSEAIDFGATSNPVTNRMASPNNMTHEMHMVHIMRGMTEDITLYAMVMLPSITMDHTRGPMNPAGGGPGSLFTTHNSGFGDTTIGALIGLYTDSNDDVILNLGGSLPTGDIFRTTSIPSGGMMEQPMPYPMRLGSGTFNARPGITWKHYFDFGSFGTQFQTDLPIGRNYRGYSVSDEFRLNNWYSQLITDNFTTSIRVENLWRTNYDGADPMSPDSMISTNVESFRGGYTLNLGLGAAALVRGHLLNVEFVPMLHQDLNGIQLETDWSIVSSWSKSF
>NZ_CP036292.1|WP_145118416.1|1455176_1458200_+|DUF5117-domain-containing-protein
MKFRNLQFALRRSASLALLLLVPGAAFADLPAFDKVSEGYKKLTSSDQQSDKTLFNVWTREKDGQMLAELPKAFAGKRYFIALTVGSGDRYAGLQSGDMVVQWRQYDERLALVLPNLEVTAKGEAEASASVKRLFTDRVLLDVPILAKGPSGGPVIDMDNLLISNASSFFGNQVRITKSRIYKIEQAKVFPENVELAYEIVGSRGQLQTIHYSFSEVPATSNGFKPRKADERVGYFTTAFTDLSKYTDDETRVRYINRWHLEKRDPKLQLSPPKNPIRFYVEHTAPVRYRRWIKQGVDYWNKAFEKVGIVDAIVIEYQDAPSGAHMEKDPEDVRYNFIRWLNNNIGTAIGPSRVHPETGQILDADIILTDGWIRHFNFNYYELMPELAMEGMSPETLAWLADNPSWDPRVRLAHPAQRLTVRESVARSSRSPMAGHSFAAANPQLMGDDEYDGLYGNISQKNGLCMAANGRRMDLALTRMNWTLALLEEEKADAQKKKKEEEEKAAAEKKKAEAAKAKKDDSKDEDKKSDEAKDDKKDDAKDEEAVAKKDDKKEEKKDDDKPKDQLLDGIPEWFVGPLLADLVAHEVGHTLGLRHNFKASSVHSLDEINSEAIKGKKTFTGSVMDYTPINFRLESGDVQGDYAMIEIGPYDYWAVEYGYTFTDADLPKILKRCHEPELQYATDEDTSGPDPLARRYDFGRDPLDYAKEQMKLVQLYRSRILDKFVKDGDSWAKARRGYELTLSKQTSAVSMMAGWVGGAFVHRDKKGDPENRSPIEVVPAEQQRAALNFVIETSFNDDSYGLTPDLLARMSVDKWLDEGFSRAMTNEATWPIHDRILGLQASALTMIMNPTTLRRVYDNEFRLPADQDTVTLPELLGTIRTAVWTELGEKCPADCSSRNPMISSLRRNLQREHLDRLIDLMLKKTDTSAAAKPISNLAMMQTKELKDEIDKSLGKCGDDMDAYTKAHLSECQSRIEQALNAGYVFNSGNQQQGPLMFILSGDEPSAE
>NZ_CP036292.1|WP_145118414.1|1453381_1454845_+|protoporphyrinogen-oxidase
MPDPAPQPTPPRHARVAVIGGGISGLVAAFDLRHRHPEWDVVLYEASDRVGGVICTLRQDDFLLEFGADSFSVQPPGAIQLCRDLGIEDRLVDPLEANRRAFILHAGKLVPVPEGFALLRPTDLKKLLASPLLSIPGRLRLVAEAFIRGKSDDSDESLQSFAIRRFGREAFDRLIQPLVAGIYTADASKLSMQATMPQFVALETEHGGMVRATRALQKQSKDDAARSASGARYAQFRSLPGGMGELFDTLVDRIDESNIRRGQRIASLQREGNSWNIESDRGEAASYDAVIVALPGPAASTLLRPLAQEAAEELAEIPYASSALVLLGVGKDQVAHPLDGFGMVVPAIEKREIIAASFLNRKFADRAPDDMHLIRVFIGGAMQSHLLERSDDELIETARRELAAMIGLQGPAKIQRVARWNNAMPQYHVGHCDRRDRVERAIGQLPGLELAGNALHGVGIAHCIRTARAAADRIGKHLASQLGDSPL
>NZ_CP036292.1|WP_145124035.1|1450669_1453369_+|DNA-gyrase-subunit-A
MVDLPIEDELRESYLTYAMSVIVSRALPDVRDGLKPSQRRILVAMNDLNLGPQSRRVKCAKISGDTSGNYHPHGESVIYPTLVRMAQEWNMRHLLIDKQGNFGSIAGLPAAAMRYTEARLSAVAAMMLDDLKLDTVDYVPTYDEARTEPTVLPGRFPNLLVNGSNGIAVGMATSIPPHNLKEICTAIIQLVENPDISIDELMDTVQGPDFPTGGIICGRGGIRRGYYTGRSTVVVRARCRIETEKKRNRIVVNEIPFQQARDRVVEKIAALVTGDRIKGIAGIRDESDLKEPVRLVIDLKRDADPDVVLNQLYQFSPLQDTFSIILLALVDGKPRELNLREILQEFVRHRVTVIRRRTQFLLARARRRKHSVEGLLLALADIDQIIQIIRASRTQPEAKIGLMGVECPASLMARALGDSGFNQFQQERGVSDTYSLTSVQADEILRMRLGQLVNLEQEKLGEEHAQLLIEISGYLEILADQQLIYDMIKEDLEEIMRRFGDNRRTEISGEELGNIDLEDLIREETMVVTISHRGYIKRVASSTYRAQRRGGKGLKGAATEEEDPIEHLFVASTHAYLLFLTTKGKVYWQKVYDLPNLSRESRGRAIVNLLQLAEDEKIAACLPVRDFNLPGHFVLMATQGGLVKKTPLENYSRPKRGGIIAIKLREGDELVKAVIIKPEDEVVLSTAKGMAIRFSESDARPMGRNTSGVKGISLGKDDHLVGLVVADPNATLLTICERGYGKRTPFGPNGDTDPTEDETSSSAKYRVQNRGGKGVRDIKTTDRNGQVIGSLRVDGDEEILMMTARGKIQRVAAEEINVIGRNTQGVRIMNLGEGDSLAAIVRVPKEEVSEEEEAAAAAPVTAADASAPASDGEAAPEAASDSEAASDDTASPDDENGAE
>NZ_CP036292.1|WP_145118412.1|1448909_1450253_+|general-secretion-pathway-protein-GspE
MAKQQEEPQLWQTVAPCEFKGIHEDSGLAQGLLISARQSPGFPVLAGQLGHAFANRATHLMLDYNAQMVNMRYQIDGMWEQLPPLPRDAGDAMLVAAKTLCRMNPADRKNAQQGKTLAIMGRDKYNVKIQSQGVPTGERVMLTLDKKDIPFKTLDDLGMRDKMQVQLKEALNDKGHMVVISAPKGGGLTTSWTIALEAADKFVSDFQAIEPKGSDEPDIINVSPNYFGPDAKNDTARDAVRALSLREPDVFVMPELYDEETIKLLHAQTKIEKQVISRIVASDAVEACARLVHKYRGAAKEIVDMLSHVTNVRLARRLCETCRQGFTPPPQLLQKLGIPQGRVAMMYQPFVPPPIEQQVDEKGNPAPLPPCPKCANRGYYGRFGIYELLTVGPKLKDALLKTSDVNKLRQVAKAEGHRNLQDEGIMAVARGTTSLEEMRRIFSSGNK
>NZ_CP036292.1|WP_145124034.1|1447400_1448654_-|prolyl-oligopeptidase-family-serine-peptidase
MLVLLLPPVLLTAQDAKDENVSQTLTAMVASAKQTPEMRWVDQTGPVHSLLYAGEDYRGKPTEVFAFYASPTTLGEGTADAKYPAVVLIHGGGGTAFAEWVWLWAKRGYAAIAMDLGGSRPSAPTFNPETGVPIANQGYPANTRTRLENGGPNQGHVEKFDSIGGEVSDDWPFHAAASVLRAHSLIRSFDDVDAERTAVTGISWGGYTTCLAASLDDRFKAAVPVYGCGFLHEGESVQKPSIDRLGDRRDDWVAVYDPGSQLRHCRVPILFVNGTNDVHYPLDSYQKSFDVVPGTKQMRIEVKMGHSHPAGWKPQEIGRFIDSYCRGGDPLPAPATPQIDGDQVTLQYTSAVPLKAANLHYTTDSGPRSKRDWQTVPAKIDGQTITAPKPPADANTWFLSLTDTRDAMVTTAVQFED
>NZ_CP036292.1|WP_145124033.1|1446094_1447387_+|MFS-transporter
MSTDQRRRAAWAFAWFFCILLAYFVIRPVRETMGIQGGTKQLPWLFLGTFTTMLIAVPIYSFVVARCQRKRLVPIVYRFFAVNLLLFWLAMHVESAQVHVWVARCFFIWTSVFSLFNTSVFWSVLADLYDSRQAKRVFGMIAVGGTLGAIVGSLLTSLLSTILGVQNLLWLPIVLLEVGVFCAGRMMRAEPPAVDVHDTDGVAESESSADAKSADDEPAPGGGIFEGITHVARSPYLAMICLFLLLGQLTGTHFYLVQAELVKEFIPERDAQTALFGKLNLFTQLLTLGLQAGVVGLVLRRMGVAAALVLLPVVCLLALIGLGLFPSIAVLAISDVVRRGVVYGVTVPSREVLFTVVDRADKYKSKSFIDTVVVRGGDAISGQAFAFVRQWHLGLAAMNALMIPVVIAWGILAIYLGRQQTRRAAAGEAD
>NZ_CP036292.1|WP_145118426.1|1464921_1466892_+|AAA-family-ATPase
MSHGLNPAQHEAVNTLSGPLLVLAGAGTGKTRVVTFRIANLIRNGTAADRILAVTFTNKAAGEMQERIAELLGISKRPSKKDDRPRPVIGTFHSQCVRILRQHATNLGYPKKFAIYDRSDQESIARSVLRELRLPTAALKPGDLLSIIGQWKNGSIHPDAAVNEARTDKEHLAAAGYRRYQNSLKACGAMDFDDLLLNTEVLFTEHEEVRQSEADRFDHILVDEYQDTNGSQYRIIKALADAHRNLCVVGDDDQSIYGWRGADVRHILNFKKDWEDATVVRLEDNYRSTGSILEMANRLIQYNTVRHDKSLKPARPAGQRPRISQFKDETEESQRVVGEIGRLIELNHYQPGEIAILFRTKEQPRLFEQELRKAALPYVMMGSQSFFDRREVRDVVAYLKWVEQPDDEVSLMRVANTPPRGLGQGTVKLLMDAAVKRGQPIWQVMCDDTVTSTLPPAARRGIDDLRGILVDVQNRIRDDGLTEAVNTLIARTRYMDEIRTRYNEPEECEARIASIGEVVNAVDAYADRAKKPSLTDFLSEIALSGREMGNEKDRAAQQNAIWLLTMHAAKGLEFPVVYMVGMEDGLLPHHRSTKGDDDAIAEERRLCYVGITRAQEKLTLSLALTRRKWGKPRPTTPSRFLYEITGQADNPNRYRK
>NZ_CP036292.1|WP_145118428.1|1466910_1467675_+|hisA/hisF-family-protein
MLSTTAESTDDDPLASVLGVIDLKEGKAVHAVRGNRDSYRPVCCAATNDGDPIALAQMYLDSDVGGLYVADLDAITAGAPHNKLLNRLADLGAPIWIDAGVVELQLPASDRIVRVVGTESIASLEELVPLRERWSARRHGIVLSIDLRERVVLGGSPALASQTAVEIASQAINSGFRRLIALDLAAVGAASGTLTLPICQAIAEKHPHVELTSGGGIRTLADIHVLKEGGCRYVLVGTALHGGRKKLSFGSGTC
>NZ_CP036292.1|WP_145118430.1|1467781_1469374_+|hypothetical-protein
MSHRVEATHAASLQNSHRARQLLAAWFVGLIAAVALGAIASPAWGQAAAGKPQYDVMKYQPNWFTEKSIVNRIKQIRSQIVSDPAQLSEQKDFFVKIYQNIFASMTDPAEFANLQPRRAEVMKDIYNAARRGNTQVSRGLSIMSFQQCKAIAQGNYYPGARINAVFMIGELNDREPNSLEKKAPIPMQAALPLLLEIVEDAKYDDGLRVAAIQGIQRHASLNAERWKPELQDKVADLMIATAQESAPKDRNLEAHGWVQMLAINTLVSLKNPRRVDQVAKLVMELPTKEDSSQMALVYAARATPKIEIPKEFKPQADAVLKSWATQIVGSIAREAKRIEDLEKPRPKASMMGMGSGEMGMMSGPEGYDMGGMEMGMEMGMGMGMPGATAAKPQTVEIILARRMLNDVIESFHLGLTGTRAKTDPARVSKGLVANLSDEKEKADAVRLVALIDEVKEGVNDTMISKNLEYAEKLRELEAKLQAFVNPDAAADPKPGNNASPFFDGPFSSAPPALNRTEPNVASRPKAAGQN
>NZ_CP036292.1|WP_145118432.1|1469351_1469999_-|SAM-dependent-methyltransferase
MKKSKPYQASEAKRGVKPKATTLRVIGGDMRGRKVRYNGDRSTRPMRDSVRESLFNLIGQRIKGSIVFDPFGGTGVLAIESISRGASRAVTMEQNRRTLEQIRQNVADLDLTERISLTAGDAFRGLGALMHQAHAEEPDTPWVFLMCPPYEMFQSRIKDLNRMICFAAEAHPHGVLVAECDNFFDTAELTAAEWDVRKYGITQLALTELSSVQLP
>NZ_CP036292.1|WP_145118434.1|1470102_1471500_+|peptidylprolyl-isomerase
MGAWDRAADWILKMRVEMSLRILAAPLLLAICLTNLAAAQESDGDQAAAAETPVAAEQPPAEDAKPAAEEKPAEEKPAAEEKPAAEEKPAADKPAAEDEKTVASPEEVKKLQAVFDQRVKEWRKATQEFWAEVNEFHTAGGDVKFSEQIRWAERESATRDAMQAAFLAASDLVFADHENRDARTFMAQSILYHAQNDWYEGLKDAALAMLEVGIKDVQLNVIAGVAAAATGDFEVAKENLKLTPAEGDEGLLKVARRMNFMLDPLQEAWEKEQKIRQAEAEADDLPRVLLKTTRGDVLVELFENEAPNTVASFISLVEDGFYSNVPFYQVVEHEFAQTGDRDGDGSGTADYRVRDEATGERGIFRGSLVLAKIPNPNAAHNPDVPGTIPDTGSSQFLITLLPFNPDYKELCCFGRVISGMGAISTLNRAKVEKEKDAPVVLPDSIIEAEVVRKRDHEYKPETLPY
>NZ_CP036292.1|WP_145118436.1|1471521_1472559_-|extracellular-solute-binding-protein
MPNTKRPLDCCRLIAPLILLVGGCVPRPENEVVVYSALDQEFAAPMLSSFDRHVDSEIQVNARFDIESTKTIGLVNRILGERDRPVCDLFWNNEIIHTVRLQKAGLLKEIDWPVDTVWPAGCIASDGTWCGFAARARVLIVNKKLLPDPDQWPTSVLDLADPKWKGQGAIARPLFGTTATHAAVLENQLGQEKADALFREIQQNAVTLSGNKQVAQAVSAGQVAWGLTDTDDAVIERDLGFPVAIVYPDQQPDQMGTLRIPNTLAVLKDAPHPVAAEQLALFLMSPETEKRLAMGNSSQIPLFRSVKEQPRVLPEESVRWLDADFEAAADRWEPLAERLNGIFVD
>NZ_CP036292.1|WP_145118438.1|1472598_1473912_+|hypothetical-protein
MLFDKPIIVAGFSPPRIGAALALCLFVAPFAAAQTRQFSGRHVTIHTDLPASAALDQLPAAFDAAVPQWCEFFGVDPDRLAGWHVTAYLMTSRDAFKQRGLLPDHLPDFAHGYQYGNSVWVVDQPSDYYTRHLLLHEGVHALMFQLFGGAGPAWYMEGMAELLATHRWSDGEIALPVIPESREAFPFWGRLKVIQSARDKGQALPIDAVMRYSHKAHRQVEPYAWSWGALTLLNMYPEYRTAAIAATDRAGQPPLQFTRNFYSELKDQWPQLQLRWRMLVDGLDYGFDPLRNRIDLTNFPAAAESSTATKQLEIAADRGWQSSGIRVAAGQAIRITAQGRYTLGDDPRPWECEPQGVTIEYHRGHPLGMLLAAVAPTSDADATRMTNPQIVGVGREGTFVAEFDGLLLLRIGDDPAALADNRGSASVTVSVAAAERP
>NZ_CP036292.1|WP_145118440.1|1473908_1474625_+|hypothetical-protein
MSRQGDDAGQLSSSPRRVGWRFSLRGLLGLVVVVTMVGSHFYTSWKLRQAMVQLKQLRSEVGYLNETDRSKLVVAVVPTDEPLTWKIRVRTPALQSYQIAYSTLWPAGSAEPTWYSGQPLPGGESLVTLRLFSDPRDNRWKIITLVRNQGNLWRMATVLSDRQAALFRGSHDAIRGGIQAETVVAAGRSLRVIEEKWFAGDGGLMLFGQEAPDDDIDGLFAELQPLPGLPFEVQENRR
>NZ_CP036292.1|WP_145118442.1|1474645_1476079_+|FAD-dependent-oxidoreductase
MPKDFLAKAADEYDVIVIGSGLAGLTTANILGRHGHRVLLLEQHYKLGGLATWFRRPGGHIFDISLHGFPAGMIKSCKRYWNDDISDRIVQLKNVRFENPMFSLTTTFNRKDFTKLLTEQFAVEQSAVEGFFDTARSMNFYDDQTTTTRQLFDRFFPGREDVIRLLMEPITYANGSTLEDPALTYGIVFSNFMSKGVFIYEGGTEDLIARMQKELKKNNVDICINCPVDKINVKNGQVESVEVHNRTIRTKSVISNSNLRSTIFNMVGSEHFDPSFVEEAEAVRLNNSSTQVYMAMKPGVEIDESCGDLLFTSTAPLFRTEALLSRDITSRTFSFYYPRTRPEGKRRYAVVSSTNARWEDWSGLSETQYEASKQELIETTVAALDKFVPNVREKIDWVEAATPRTFNHYTRHQLGASFGTKFEGLAVSRKLPEQIGGLYHAGSVGIIMSGWLGAINYGVIVANDVDQRLMKQEAAPA
>NZ_CP036292.1|WP_145118444.1|1476142_1477600_-|MFS-transporter
MDTSASSLADREPSELANDQPAVVPRRYLLAFILTTCCFSMWGFANDLTNPLVKVFKEVFQISNTQSSLVQFAFYSGYFTMALPAAFFIRRFSYKGAIMVGFALYAVGALMSIPASLNTNFWIFIAGFYVLTFGLAFLETSCNPYILAMGPAETATRRLNLAQAFNPIGSLTGMIVASLLIAPALNIGSFRDAVENRDPAAVQYLHAEYPDGLPDFATEFGALDSAASAGLKNMKATAPEEFLAIQTHDLAVVRTPYVAIAAVALAFLGLFAVAKMPDFRQPEPDAPFFEIVGRLLARPNYREGVIAQAFYVGAQITCWTFVIHYGMEQVGLTLAQAQNWNIAAMVIFLISRFICTFLMHYVSAGRLLALFAIAAVGFTLGAILLPGKTGLICLVLVSACMSLMFPTIYGIALKDLPEEEAKLGSAGLIMAIVGGAVLPLLQGKFIDELGVRSSFYLPLICFVVIALFGIRTFTKFERPDVATDH

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Crispr_ID: NZ_CP036292_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_10

2099455-2099561

Orphan

Consensus_repeat	Method
CGCGGGGCGTTGCCCACGCGGTTAAACGATTTATG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_10

>merge|NZ_CP036292|10|2099455-2099561|CRISPRCasFinder
CGCGGGGCGTTGCCCACGCGGTTAAACGATTTATGCGCGGCGGCGCTGGAGTGGAGGCTTTAGCCGAAGCCGCGCGGGGCGTTGCCCGCGCGGTTAAACGATTTATG

>NZ_CP036292|10|10|2099455-2099561|CRISPRCasFinder
CGCGGGGCGTTGCCCACGCGGTTAAACGATTTATG	CGCGGCGGCGCTGGAGTGGAGGCTTTAGCCGAAGCCG
CGCGGGGCGTTGCCCGCGCGGTTAAACGATTTATG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145119237.1\|2099615_2100887_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379311
NZ_CP036292.1\|WP_145119263.1\|2107338_2107635_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119241.1\|2102602_2103868_-\|exo-alpha-sialidase	unknown	unknown	gnl\|CDD\|271234
NZ_CP036292.1\|WP_145119257.1\|2103925_2105416_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|312856
NZ_CP036292.1\|WP_145119233.1\|2097170_2098073_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119235.1\|2098107_2099250_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|238141
NZ_CP036292.1\|WP_145119223.1\|2089143_2090457_+\|tetratricopeptide-repeat-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119231.1\|2095780_2097169_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293764
NZ_CP036292.1\|WP_145119259.1\|2105491_2106163_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119221.1\|2085558_2088759_+\|protein-translocase-subunit-SecD	unknown	unknown	gnl\|CDD\|237276
NZ_CP036292.1\|WP_145119267.1\|2109722_2114531_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145124060.1\|2090492_2091389_-\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|223786
NZ_CP036292.1\|WP_145119225.1\|2091594_2092302_+\|bacillithiol-biosynthesis-deacetylase-BshB1	unknown	unknown	gnl\|CDD\|274915
NZ_CP036292.1\|WP_145119229.1\|2094020_2095532_-\|carboxypeptidase-M32	unknown	unknown	gnl\|CDD\|341054
NZ_CP036292.1\|WP_145119228.1\|2092356_2093694_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036292.1\|WP_145119265.1\|2108145_2109678_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293754
NZ_CP036292.1\|WP_145119269.1\|2114700_2116017_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340913
NZ_CP036292.1\|WP_145119219.1\|2085111_2085486_+\|preprotein-translocase-subunit-YajC	unknown	unknown	gnl\|CDD\|235518
NZ_CP036292.1\|WP_145119261.1\|2106206_2107133_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119239.1\|2101070_2102417_+\|acetylxylan-esterase	unknown	unknown	gnl\|CDD\|368448

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145119237.1\|2099615_2100887_-\|hypothetical-protein	gnl\|CDD\|379311	pfam13646, HEAT_2, HEAT repeats. This family includes multiple HEAT repeats.	3.96322e-05
NZ_CP036292.1\|WP_145119257.1\|2103925_2105416_+\|hypothetical-protein	gnl\|CDD\|312856	pfam09492, Pec_lyase, Pectic acid lyase. Members of this family are isozymes of pectate lyase (EC:4.2.2.2), also called polygalacturonic transeliminase and alpha-1,4-D-endopolygalacturonic acid lyase.	1.16924e-23
NZ_CP036292.1\|WP_145119235.1\|2098107_2099250_-\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|238141	cd00229, SGNH_hydrolase, SGNH_hydrolase, or GDSL_hydrolase, is a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the typical Ser-His-Asp(Glu) triad from other serine hydrolases, but may lack the carboxlic acid.	3.68134e-22
NZ_CP036292.1\|WP_145119265.1\|2108145_2109678_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293754	cd16030, iduronate-2-sulfatase, iduronate-2-sulfatase. Iduronate 2-sulfatase is a sulfatase enzyme that catalyze the hydrolysis of sulfate ester bonds from a wide variety of substrates, including steroids, carbohydrates and proteins. Iduronate 2-sulfatase is required for the lysosomal degradation of heparan sulfate and dermatan sulfate. Mutations in the iduronate 2-sulfatase gene that result in enzymatic deficiency lead to the sex-linked mucopolysaccharidosis type II, also known as Hunter syndrome.	0
NZ_CP036292.1\|WP_145119231.1\|2095780_2097169_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293764	cd16145, ARS_like, uncharacterized arylsulfatase subfamily. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036292.1\|WP_145119221.1\|2085558_2088759_+\|protein-translocase-subunit-SecD	gnl\|CDD\|237276	PRK13024, PRK13024, bifunctional preprotein translocase subunit SecD/SecF; Reviewed.	1.9961e-101
NZ_CP036292.1\|WP_145119267.1\|2109722_2114531_+\|tetratricopeptide-repeat-protein	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.	4.55377e-81
NZ_CP036292.1\|WP_145124060.1\|2090492_2091389_-\|AAA-domain-containing-protein	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	7.14875e-88
NZ_CP036292.1\|WP_145119225.1\|2091594_2092302_+\|bacillithiol-biosynthesis-deacetylase-BshB1	gnl\|CDD\|274915	TIGR04001, thiol_BshB1, bacillithiol biosynthesis deacetylase BshB1. Members of this protein family are BshB1 (YpjG), an enzyme of bacillithiol biosynthesis; either BshB1 or BshB2 (YojG) must be present, and often both are present. Bacillithiol is a low-molecular-weight thiol, an analog of glutathione and mycothiol, and is found largely in the Firmicutes. [Biosynthesis of cofactors, prosthetic groups, and carriers, Glutathione and analogs].	2.44024e-76
NZ_CP036292.1\|WP_145119229.1\|2094020_2095532_-\|carboxypeptidase-M32	gnl\|CDD\|341054	cd06460, M32_Taq, Peptidase family M32, which includes thermostable carboxypeptidases TaqCP, PfuCP and FisCP. Peptidase family M32 is a subclass of metallocarboxypeptidases, distributed mainly in bacteria and archaea, whose members contain a HEXXH motif that participates in coordinating a divalent cation such as Zn2+ or Co2+. It includes the thermostable carboxypeptidases (E.C. 3.4.17.19) from Thermus aquaticus (TaqCP) and Pyrococcus furiosus (PfuCP), which have broad specificities toward a wide range of C-terminal substrates that include basic, aromatic, neutral and polar amino acids. These enzymes have a similar fold to the M3 peptidases such as neurolysin and the M2 angiotensin converting enzyme (ACE). The keratin-degrading extremophilic eubacterium Fervidobacterium islandicum M32 carboxypeptidase (FisCP) plays an important role in cellular metabolism, and significantly enhances the degradation of native chicken feathers. It has been shown to mainly cleave the C-termini of peptides with a basic amino acid sequence. Novel M32 peptidases from some eukaryotes: protozoa Trypanosoma cruzi, a causative agent of Chagas' disease, and Leishmania major, a parasite that causes leishmaniasis, have been identified, thus making these enzymes an attractive potential target for drug development against these organisms.	0
NZ_CP036292.1\|WP_145119228.1\|2092356_2093694_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	4.8895e-16
NZ_CP036292.1\|WP_145119269.1\|2114700_2116017_+\|MFS-transporter	gnl\|CDD\|340913	cd17355, MFS_YcxA_like, MFS-type transporter YcxA and similar proteins of the Major Facilitator Superfamily of transporters. This group is composed of uncharacterized bacterial MFS-type transporters including Bacillus subtilis YcxA and YbfB. YcxA has been shown to facilitate the export of surfactin in B. subtilis. The YcxA-like group belongs to the Monocarboxylate transporter -like (MCT-like) family of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	7.37455e-35
NZ_CP036292.1\|WP_145119239.1\|2101070_2102417_+\|acetylxylan-esterase	gnl\|CDD\|368448	pfam05448, AXE1, Acetyl xylan esterase (AXE1). This family consists of several bacterial acetyl xylan esterase proteins. Acetyl xylan esterases are enzymes that hydrolyze the ester linkages of the acetyl groups in position 2 and/or 3 of the xylose moieties of natural acetylated xylan from hardwood. These enzymes are one of the accessory enzymes which are part of the xylanolytic system, together with xylanases, beta-xylosidases, alpha-arabinofuranosidases and methylglucuronidases; these are all required for the complete hydrolysis of xylan.	1.00765e-45
NZ_CP036292.1\|WP_145119219.1\|2085111_2085486_+\|preprotein-translocase-subunit-YajC	gnl\|CDD\|235518	PRK05585, yajC, preprotein translocase subunit YajC; Validated.	1.50327e-20
NZ_CP036292.1\|WP_145119241.1\|2102602_2103868_-\|exo-alpha-sialidase	gnl\|CDD\|271234	cd15482, Sialidase_non-viral, Non-viral sialidases. Sialidases or neuraminidases function to bind and hydrolyze terminal sialic acid residues from various glycoconjugates, they play vital roles in pathogenesis, bacterial nutrition and cellular interactions. They have a six-bladed, beta-propeller fold with the non-viral sialidases containing 2-5 Asp-box motifs (most commonly Ser/Thr-X-Asp-[X]-Gly-X-Thr- Trp/Phe). This CD includes eubacterial and eukaryotic sialidases.	4.17981e-10

>NZ_CP036292.1|WP_145119235.1|2098107_2099250_-|SGNH/GDSL-hydrolase-family-protein
MKIKLLPIVILLVCNPFRSGETSAEETSTWKYTPAALQPFWAGDRIEGESVLFVRDAKTGEARGSLLFPIAEIESVKSSSGKITYREGTDYRFKPGTREIVVPAGSQIVTTLPEELRRPAKSQRHQLTHRDGNGEILFGATLEYHQMQTLVTYKTSEKNWPVAAPKFDPAALPTTIGKLRDEKPLSIVLLGDSISTGCNASGWGGGAPFQPAYQDLLLQHLKTQYSPNITLTNLSIGGKATPWGVSMIDEVASHKPDLVIIAFGMNDSAGISAENYGKYTAEMIAKTRAQLPEAEFILVATMLGNRDWIRLNHDVFPQYRDTLASLCEPGVTLADMTSVWEEFFKRKKDADLTGNGVNHPNDFGHRVYAQVLSALLVDSE
>NZ_CP036292.1|WP_145119233.1|2097170_2098073_-|hypothetical-protein
MKLHCLAMFVAILLAQSTPLHADTEAATARRLEALGATVVIKADRIVELSFRDSKRLESQQWQEIGSLTHLKKLTAYGGAKGLNDETVGFLVGLQELESLSLDGAQLSDAGLAKLAELKRLKRVSFFHLSFRKEGFTGEGFSAWTELPDLESLTVAGMSMGDDGFRAIATLTNLRQLRTWHTYRTEASNAEIAKLPRLTTLKLGQRLPQRGNAPLSLSDASLETLTQIKTLETLEIGEADFHLPALRQLTKLPRLKRLKIDRTYLSAADIEALKSALPGVQIGFEPLIEDQRKKLDAYLK
>NZ_CP036292.1|WP_145119231.1|2095780_2097169_+|sulfatase-like-hydrolase/transferase
MKTRPLFLLLTLWIVPLAALAATADQPHPNIVYILLDDAGYGDLSCYGQKKFETPNIDRLAAEGMKFTQHYSGSTVCAPTRCCLMTGVHTGHAYVRGNREIKPEGQAPMPADIVTLPRLLSAAGYETGAFGKWGLGGPGSASDPAEHFDLFYGYNCQREAHNYYPDHLWKNRQRVPLDGKTYTATMIGDEGLDFIRANKDQPFFAFFPVAIPHAAMHAPESYIAPFREKFPEFENKIGKYAGPEVKNPIAAFAGMMTLVDEQVDQIIALLKELDLDERTIVMLSSDNGPHREGGHDPDFFDSNGPFRGYKRDLYEGGIRAPLIARWPGKISPGSTSDLISAHWDMLPTFCELAEAKTPDTIDGISLVPTLLGDDDKQQPHEFMYWEFHERGGKRAVRFGDWKAVQLNLNKKQRGEIELYHLPSDRGEQKNVAAEHPELVAKAKAIMLSAHQPSEHWKFKGGK
>NZ_CP036292.1|WP_145119229.1|2094020_2095532_-|carboxypeptidase-M32
MNGNETFDQLAKFTRETALLESISYTLEWDERTYMPTGGRAYRADQVTYLAGMAHRRRTDPQMGDWIAELQQSELAGDRHSDAGATIHRIGRDFERACKLPQDLVEALSRATVVGQQRWEDARKADDFAAFLPALEEIIRLKIESAERLADGGNLYDALLDEYEEDAKSEQLTEVFRDLRSELVPLVAAIRDAKTQPNTDLLRRNFPVDAQRKFCMQAAEAVGFDFTRGRLDETSHPFCTSLGPSDCRILTRYDAHWFPGALYGTLHEAGHGIYDQGLRGDQFGLPPGTYVSLGIHESQSRMWENMVGRSLPFCQHFYGELQRTFPEALSDVDVNAFHFAVNTVEPSLIRVEADEVTYNLHIIIRFELEQALISGDLKPKDLPDAWNQKYQEYLGITPPNNADGVLQDVHWSAGLLGYFPTYTLGNLIAAQLFDAAGEALGDLDAMFGKGEFTPLRSWLNENIHHHGRVYSPNELVQRATGKPITSQPLVGYLKRKFGSLYNL
>NZ_CP036292.1|WP_145119228.1|2092356_2093694_-|PQQ-binding-like-beta-propeller-repeat-protein
MNTLPFCRSLGVVATLLLTTQIVAAVEWSQFRGTAGDGIADVTHAPTQWSETENVIWKTPIAGKGWSSPVVADGKVWMTTAIEEQATEEERIATLERLVENPRRFGEFRLAKSITLRLVAVDLATGAQEMEIDLVRLDQPDPIHTINSYASPTPVIDGDNIYCHFGTFGTICVDRKKGAEVWRKRLPLEHGVGPGSSPFVYKNALVLICDGMDQQYVTALDKSTGETLWRTDRPPLDAASGEQKKSYDTPIAIIDAAGREQLICMGSQWLVAYNPTDGSEIWKVRHGKGFSVVPRPVYGDGTVYISTGFGKPQLWAIRVDGSGDVTDTHVAWVEKKGIPAKPSPLLIDGELYVISDDGIASCFDAASGELVWKQRVGGKYSASPLMAAGKIYLCSHEGKVSVLKPGREYQLLAENQLDGQLMASPAALGDSLLIRSDTALYRIAE
>NZ_CP036292.1|WP_145119225.1|2091594_2092302_+|bacillithiol-biosynthesis-deacetylase-BshB1
MIENPPKLDALVIAPHPDDAELGMGGAIVKMLSEGLKVGVLDLTSGEPTPFGSPETRREETAAATKALGLSWRHNAGLPNRSLEPTLAARELIAGIFRLTKPRWLFAPYWEDAHPDHIAATALVEAARFWSKLSKTEMPGEPYHPERIYYYYCVHLKLTPQPDFILDISDQWETKRKSIEAYQSQFVVGRDPAPPTFIDRLRDEAAYWGKAVGCRYGEPFASREPVALRSMRELF
>NZ_CP036292.1|WP_145124060.1|2090492_2091389_-|AAA-domain-containing-protein
MEKVVLGKPEVVRSLLIAVLAGEHVLLDDVPGVGKTLAAKALARSLDGVFTRVQFTPDLLPSDIVGSNLYRTDLHEFEFNQGPVFANVVLADEINRAPPRTQSALLEAMSEGQVSIDGTTRPLPKPFTVVATQNPIEFEGTYRLPESQLDRFLLRTSVGYPQPDVERDVLRSHCDGEPVEQLSPVATCEEVLQSQEAVRRVRFEDSLISYLLAVVDATRQSEDLQVGVSTRAALSFFRGCQARAVCMERDYVVPDDIKSLAVPVLSHRVVLKDSFMTGDRLRAEQIVGEIVHRVTVPV
>NZ_CP036292.1|WP_145119223.1|2089143_2090457_+|tetratricopeptide-repeat-protein
MTHSTALTNEPNHWCCALSDRYRFTLSADLVDWFAREIWLRDQGGEFDQPVSPSELLCETPDFIWPGFMLPDSLPLVGNRYGDWLCLRVGADNSVAEVIHWYHGGGDWMPWGATLAEAVAFDSLRSRLPGRRQYYANIAADFAQQSGPATIPGWAADHLPAAIGKLLLDESGDTDEIPGLGELMIQHDVASTAVHGESALAALDSLLRQKLEPWAARELGIQWDQDAIRWLFDNDLIQPSVLQRLADHFGCDSEDLRGQDWDVAIAHATAVVAKRDDLGWASDILGWAAERAGRPDAAIAAYRNSLRCSSFADQSVRFRTHWFRESEGKFAAARLQELGADLQHDSYLRLFRESKDQGLRSRVTNYWMRIAEQAASDERWAEAYDAYYRAGWDMGCDDLEVYEELLSRLADAAERSGMVARAALAKTHLACLANRLR
>NZ_CP036292.1|WP_145119221.1|2085558_2088759_+|protein-translocase-subunit-SecD
MLDLNVIETLLAQAEPGKLGTQIGIIAIMLAVLIVPFLVGAFLAKSLRMPNYGTRIGVVLFAITASVVTITFGQLKYGVDLKGGTILVYEIDPTAGGGASDDPSSRVTAEELVGALTERINPSGTQEIVIRPYGDRQIEIIVPNVEESGVNEIKDKVQTAGMLRFAIVANERDHLGLIETVRAAGPTLSDVVKDDAGEVIGQWVKVDRESEEILGGLRPFRVEVSGDIIRDSRTGTLLTPQGLQGENALVKWLSQNGIEDIDVLMRIEKEYDITGEDLAIVASDHDGQGNPAVRFTLNAAGKKRFYVLTMNNSPDGSFLRRLGIVLDDKLLSAPVIRSPINGDGQITGNFSREEVDFLVGILRAGRLPAALSKQPISENQIGSTLGDDTIQKGKWSIISAFGLVLFFIGVYYRFAGLVACFALLLNLAMILAMMILINQPATLPGLAGLVLTVGMSVDANILIFERIREELRRGAAPRMAIRNGFGRATTTIVDANLTTLITAIVLYTIGTDQIRGFAVALILGILFSMFTAIYVSRTFFDIAERWGRVSLGMSDVVTSIRTAVTGNADFDFIGKRVPAFFLSATLMIAGVIALAYRGGSIFDIDFAGGTSVTFWLQSDAESDEVREVVESSLNTDPESKIQFSLNSVDMAGMKNRVFAIYTSVEDVDDLKQRIREGFEASDDLDLVTFETAITDADAAPAPEAEATGQIGRNDASLIRTVAYRPQDDAADAPADTADGEAAADATAADTAAEEATEAAAGEGPSISAAVEKPKTESTTRVLALGVAGGDQNDAKINHDALVAAVVKAAAAREIPLQEEGIVVVPQGAGSEDWSDESNMGFAQWKVTLDLPEANATAVLDGLKSELDAGPIWLSSSKVGSRVAGDMTRRAIAAMLASLVFIVGYIWFRFQRVAFGFAAVVALVHDVLITLGAIAVSFWAARYLGFLLIDEFRISLAVVAALLTIIGYSLNDTIVVFDRIREVRGKSPNLTAEMVNTSINQTLSRTLLTSLTTLLVVVLLYAFGGEGIHSFAFALTIGVIVGTYSSIFVASPTLLWLFNRTEEATTR
>NZ_CP036292.1|WP_145119219.1|2085111_2085486_+|preprotein-translocase-subunit-YajC
MTFMVPIGNRIGLLAQDAVPVEGPAWQQILFNPIGMITILVVLFYVMVLLPERRNRNELTKRLAALKKNDRVVTVGGIHGTIVNITESDQVVIRVDENNNTRLHVNRSAVSRVISDDDDKSVKP
>NZ_CP036292.1|WP_145119237.1|2099615_2100887_-|hypothetical-protein
MRYNRSPPNSNLPTPSEPMFSIKFVIRFALAWLGLFALPASAETRQLELHAAIESGAVSVRIEFLGGALGDRMKIYLRKQTAGDLQLKVTPGTLFLPQGGDVQRLAAVGLKGKLTAQGTYRRTAAIELNDSSEQGFLTQVVCIDYHKNSPPAGQAFITGAVEPRCQRILSVRGDLSIWAYQSAIWIDRAGVSPSKLQATFQVASTDLQAAADLLKEAEAAGAASLAEVDVSVEAKASARGIFSADPAVRAQAHAEVQTLDPADRAKLDALLKLNVLRGGKLPTAEELRAGSTLESLIPAGIELPKLEIPQSVDDIMAMVDAIRQQAADGQAGDKIADLASLKLLPHLAGLKARLPLLRIAAARAIANVKDPVAVEALLVALQDRDARVRAAAAAGLEKLTQQNFGDDTEKWTAWWQEAHVSFE
>NZ_CP036292.1|WP_145119239.1|2101070_2102417_+|acetylxylan-esterase
MRRFSALRSHAMLLAFALPIFLSTASLAAAEGYAVSVAADRDDAIYDSGEAAAFVISVTRGDQPVTDGKLTYVVDDFLRSGKSGGYPEGEASLDGKPVRVAVKSDKPNVLRCQVTYTPAEGKPIRRLAGLAFSPTEIEPSMPVPDDFDAFWADQKKQLAEVEITPTLTPVEQKNNKIACFDVQVPCLGGAPVSGYFAKPVGAEEKSLPAILWVHGAGVRSSSLYAATKGANAGMLSMDINAHGIPNGKPAEFYAQQSGGPLKNYRYAGRDSRDTIYFRGMFLRLVRAIDFLTMQPEWNGREVIVIGHSQGGGQALVAGGLDPRVTLIASGVPAICDHTGNVAGRVNGWPKLVPNGPDGKPEPAALEASRYVDSVNFASRCKADAIMSVGFVDVTCPPTSCYAAYNALLGEKTMISEPLMGHNAPKHIHKAFFDRVLQHVEQSQPAAAK
>NZ_CP036292.1|WP_145119241.1|2102602_2103868_-|exo-alpha-sialidase
MRTVSLSVIPKHHLRIAIIIAICMGANLATLARADEPLIASISKQTLWENRDGKGATWFHPRVCMMPGPDGKPIALMTIQEIGGSDYFGPVCWSTSTDLGKTWSDPEPIPALGRDPIPGRSDDLKAAVCDVVPQYHPQSNSVLALGHVVFYKGKYFARKEQLSRYPVYATRAADGTWSQRKILEWEDPRNTSIYSNGCGQRVVLPNGDVQMSFTFGPGEKNRMVAGVHAAYDGDQLTMREIGPPLENRHGRGLLEPSVTEFDGKFWMTIRAEDDHGYVSSSEDGLNWSPKKAWAWEDGTPIGMSTTQQHWLTHSDGLFLVYTREDESNANVMRWRAPLWVAQVDVQRQCLIRETEQVALPLVGDGVNDPKKVALMGNFHVTHASPDESWITVGEWMPWNGYRGDVLLARIRWSRPNRLPLW
>NZ_CP036292.1|WP_145119257.1|2103925_2105416_+|hypothetical-protein
MATLYRMILGRRSSLGSMVCALAAAIAIVAAPIPRGYGDEPPTREEAVQAMHRAVAFFRDQASAGGGYVFGLSEDLSLREGEGKVGHSTAWIEPPATPAVGLAYLNAYRLTNDPILLDAARKTATALINGQLVSGGWGEQIEFAPRDRARYAYRVDSMEVGKRRNTSTLDDNKTQSSLRFLMQLDSTLEFRDAKLHEAARFGLDRVLTAQYRNGAWPQRFDGPNDQAEVPVVKASFPEQSPKTFPKQKYDSFYTLNDNTHCDAIATMLEAWDTYQDPRYKEAAIRGGDFLLLAQLPQPQPGWAQQYDYQMHPVWARKFEPPSISGGESQGAMQMLLHLYRRTGDKRYLQAVRTALPYFNRSLREDGRLPRFLELQTNRPLYLTRDYAVTYNDNDLPTHYSFVVKARLDSIEKELNKLESLPPDQLWRPGKRKSPKMSDALSKAASQRIDSLDQRGAWVEKGKLKTHAQTPGGRIISSTTFIKNLDVLAEYVAAANR
>NZ_CP036292.1|WP_145119259.1|2105491_2106163_+|hypothetical-protein
MKTMPDASEPIDPYHKWLGIPKPQQPPTHYRLLGIEPFENNPEVIDAAASRQVAYLHQLTSGPHRRLTQKLMNEIAQARRVLMDDASREKYDAQLRDRPAEKPASPKPENKIDFGTFPAIDFGEKKTRKPIDTDSFAVVTDQSSEEPAASIGDSGASRPRGGRAPKAWWQKNDWRIHLGISAISVAIFVVYLLFWGPGSNNRFVPEGNFEQPKIQNFDDQFID
>NZ_CP036292.1|WP_145119261.1|2106206_2107133_-|hypothetical-protein
MTRIAFSASLPMTLLLAVLVGSAGAQQTNNASPAVQAEPAYLLHYQLKAGETLQYQVTHVAKTKTRIRGKDELTNVRSLSTKVWNVESVDPATGQMTFVHMVQDTELSQKIGEADEVRWDSKSGEDPPYQFEAVKATLGKPLTTVSINGQGQEKERESHAGTKANLGMGGLTLPLPPKAIKVGDTWAVPRQTHARLAGGQVKRIDVRELYTLKKVQTGVATITVQSQPITPISDPKVKSQVVQQLSNGTIKFDIDAGRVLSKQLDWDETVVGFEGAESMMEYRARLNETLVETKTSVAARSIDQLKLK
>NZ_CP036292.1|WP_145119263.1|2107338_2107635_-|hypothetical-protein
MSEKKPTPWRVQESGKVCPICGKRTYSNGGIHPQCAVLQADSARTEKLRAERKRKASEASSNPKAKPHSTSWTQKKCPKCGKESHVRRKNCDCGHAFE
>NZ_CP036292.1|WP_145119265.1|2108145_2109678_+|sulfatase-like-hydrolase/transferase
MVRIQTSFALAIGTCLLSAAIAAGGDRPNVLLICVDDLKPTIGCFGDPVAVTPNIDALASRGVRFDAAYCNQAVCSPSRNSLMTGLRPQTIGVYDLGTHFRLAVPDAVTFSQYFKQHGYRAEGLGKIYHTGHGNVNDKASWSVPLWRPKAAQYVLPESLQNHRPDSKGRNRGPATEAADVSDETYADGKIAREAIARLTAASKRQDQPFFIAVGFLKPHLPFVAPQKYWDLYQPDALPMPEVVVPPTGAPSYAAVKGGELRSYSDMHDKKEIDPQTTRHLIHGYYAATSYADAQIGRVIDKAKQLGLLDNTIVVLWGDHGWHLGDHGMWCKHTNYEQAARIPLIVAAPKSQRDLVSNSLVETVDIYPTVAELAGLPQPKGLDGISFANLIEKPDAATRDHVTHVYPRGSRLGRAIRDSRYRLVQWKSPGGKDATAELELYDYQTDPLETKNVASENPEVVARMLDLLAQQPEAKRQWKAKGKSGSNSNGKGAKKTPGKPKPVSTDEKTGT
>NZ_CP036292.1|WP_145119267.1|2109722_2114531_+|tetratricopeptide-repeat-protein
MSAASHRNLLVGALAVQLRLIDVGDVAAAIVRWTEDKSQSLEDLLHAENRIDAQTKQLLTSLVDKQIELHQGSTEAALGTICPPSEPSLSTLYQSLRPIEDADVTDSLNSVSDIAAESIDPWATNFHPTTSDELPSDAAAASHRTRYQKLRDHAKGGLGQVYVARDEELNRQVALKQIQARFSGDQGARQRFILEAEITGGLEHPGVVPVYGLGVYEDGQPYYAMRFIRGQSMEAAIASFHQRFPKTGAPAWRDPERTLELRKLLSRVLDVCQAIAYAHSRGVLHRDIKPDNIMLGKYGETLVVDWGLAKVAGLDDVESEAVDEPHLAPASGSDSAPTRFGSVIGTPGYMSPEQASGEIDAIGPASDVYSLGASLYCLLVGKPPFQSRDADGNPLTITQLLEKVRNSEFTAPRQIDPAIPKPLAAICVRAMAKDPENRYANPLELADELERWMADEPVTAYRESGLQRLRRWVKRHQTLAAASAAIVLVSVLGLSSFSVVLGKKNIQLAELADSLSTKNQQLDQRGQELQKSNEELRIAEAEATEKAAIATAVTEFLNDDLLSQASPAKNPDPQLQVRTLFEQALQGMQDRFSDQPLVKAKLLHTIGVASGYLAQWGESEAALAEALRLRTEFLGPQDVETLKTEAALGQVAASRGKYAKARTLLTSTLQTQLSELGDEHPDVFETQNGLAGLYSLLGEFDKAHELNEQAIAGYTKSFGPDAAETLDCLITKVGLLAAAGRFADALQLSSDVHTRAAAGLGPMHFTTYDALLSTAQQMYSLDRPDDAYDVYTTFLKELIETQGESHPYVAIVRNDLALIDSDQGDPVQGLATLRELARESIQTLGPAHRDSIMSQFNVGTALNALGRFEESQPIFESALKTADESLGPVSPSALQTRFLLAQVHWELGDSEAAQPLLEEVIALAKTPMQVESKVVLDAKTLLASIYGAAAKYDEARELLLAVRAGYAKLGLGKSRVMVYPTEYLIDVLVYSDRTDELDELLQQLDDDFGADSVLANQLRLRMAENWIERGEIDRADVSIQQVTQWLADRDPLERSEFGVAYYLAGLMSMLKRSQQAIDVYERLVVRQSEVLGANHVDRLLTLHDLAFEYSEFGQHKESAKLYTEVVRRRTEVYGLESDQTLQSLYNLAMEQFALEDHQGTIESMKQLVKAAEARGEPIVNRMELHTGLAHALMKTKDYAAAVPHFQAGVEGMIETYGEADDDTLLLMHQLAYCMDAAAQPEESIAMYRRVVDGRSEVLGAAHGHTLMSLGNMAQVQATAELEQGAEESIADMQRRIESLDVGDVVAIDANYAIAETYRKMNRLDDAITFYRKVADGRRTSLGEEHERTLLAMHQVAYTCGLAGKLDDAVVIYAKVVAGRSKTLGRTHPHTMLSLNNAAKIEMGRRKPAKAAALYEDILNRIVEDKGLRHTDTLLPRMELANLKYQLREYAMATELYSLSVDVMRKSLGKTPTETMREGFAGVLVMLADAEAHDGQFLAAGRHAREGLEMLEIVAPENWLRYRSLSVIGGLQAADGQHAEAQASLQQAYEGLAASDWKAVELLNQVQIETVDRLLDSYTQTNNADQVAKWKQVKESLTEQPQP
>NZ_CP036292.1|WP_145119269.1|2114700_2116017_+|MFS-transporter
MTTSIHTPALRVPQGFFYGYLMVPVASLAQICTAPGQTFAISAFIPAIRDSLQLSEISLTSAYMIGTLVAAFPLMLVGPIADRIGNRATITGIVLLLAGACFFASFVNSFATLLLAFLALRFLGQGSLSLLSSNTTSMWFRTKLGRVSAIMSIGMAGAFAVIPGWLLSSIESYGWRETYRGLGLVVAGIMLPLLAIVYRNRPEDVGQHLDGNRPDEPLPHAEGSRATGSQRTVAIEERSLSLRDAMRQPTFWILMTIMSAWAMIGTGLVFYLFAIGEARGIDKDATAAVFKTFALSMLAMQFSGGFLADRFALHHLLFAGVGLLSLGTLTLFFAQTSPQLHLFGLLFGAGQGITVAVNATVWVRYYGRAHLGKIRGTSWSASVAGSGAGPFLLGWAKDHSGHFEPAIIAFLCILIPLVLLALWVRPPARPDVLAPAAS

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Crispr_ID: NZ_CP036292_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_11

2259238-2259334

Orphan

Consensus_repeat	Method
TACGCCTTGGCGGCGGGGACTTTA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_11

>merge|NZ_CP036292|11|2259238-2259334|CRISPRCasFinder
TACGCCTTGGCGGCGGGGACTTTATACATTTTGGTGCCGGTCGTAGGCAGCACGGACGATCAGGTCGATCTTTTACGCCTTGGCGGCGGGGACTTTA

>NZ_CP036292|11|11|2259238-2259334|CRISPRCasFinder
TACGCCTTGGCGGCGGGGACTTTA	TACATTTTGGTGCCGGTCGTAGGCAGCACGGACGATCAGGTCGATCTTT
TACGCCTTGGCGGCGGGGACTTTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145119425.1\|2256466_2257552_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119431.1\|2260472_2263160_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119443.1\|2271971_2272799_+\|phytanoyl-CoA-dioxygenase-family-protein	unknown	unknown	gnl\|CDD\|368580
NZ_CP036292.1\|WP_145124074.1\|2264923_2267509_-\|heavy-metal-translocating-P-type-ATPase	unknown	unknown	gnl\|CDD\|319851
NZ_CP036292.1\|WP_145124071.1\|2254185_2255352_-\|AMP-nucleosidase	unknown	unknown	gnl\|CDD\|350162
NZ_CP036292.1\|WP_145119429.1\|2259907_2260399_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227902
NZ_CP036292.1\|WP_145119419.1\|2249799_2250429_+\|DUF3124-domain-containing-protein	unknown	unknown	gnl\|CDD\|378638
NZ_CP036292.1\|WP_145119423.1\|2253268_2254177_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|320024
NZ_CP036292.1\|WP_145119441.1\|2270932_2271685_+\|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|336781
NZ_CP036292.1\|WP_145119435.1\|2264714_2264927_-\|cbb3-type-cytochrome-oxidase-assembly-protein-CcoS	unknown	unknown	gnl\|CDD\|377073
NZ_CP036292.1\|WP_145119415.1\|2247312_2248587_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145124073.1\|2257567_2259028_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|368090
NZ_CP036292.1\|WP_145119417.1\|2248937_2249816_+\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|225797
NZ_CP036292.1\|WP_145119433.1\|2263323_2264700_-\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|365823
NZ_CP036292.1\|WP_145124070.1\|2251319_2252699_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238362
NZ_CP036292.1\|WP_145119437.1\|2267589_2269047_-\|anthranilate-synthase-component-I-family-protein	unknown	unknown	gnl\|CDD\|223225
NZ_CP036292.1\|WP_145119445.1\|2273011_2274373_-\|ribosome-biogenesis-GTPase-Der	unknown	unknown	gnl\|CDD\|274667
NZ_CP036292.1\|WP_145119421.1\|2250553_2251261_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145119439.1\|2269103_2270225_-\|3-oxoacyl-ACP-synthase-III	unknown	unknown	gnl\|CDD\|181732
NZ_CP036292.1\|WP_145124072.1\|2255449_2256268_-\|heme-dependent-peroxidase	unknown	unknown	gnl\|CDD\|237033

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145119429.1\|2259907_2260399_+\|hypothetical-protein	gnl\|CDD\|227902	COG5615, COG5615, Predicted integral membrane protein [Function unknown].	0.00389294
NZ_CP036292.1\|WP_145119439.1\|2269103_2270225_-\|3-oxoacyl-ACP-synthase-III	gnl\|CDD\|181732	PRK09258, PRK09258, 3-oxoacyl-(acyl carrier protein) synthase III; Reviewed.	2.99884e-156
NZ_CP036292.1\|WP_145119443.1\|2271971_2272799_+\|phytanoyl-CoA-dioxygenase-family-protein	gnl\|CDD\|368580	pfam05721, PhyH, Phytanoyl-CoA dioxygenase (PhyH). This family is made up of several eukaryotic phytanoyl-CoA dioxygenase (PhyH) proteins, ectoine hydroxylases and a number of bacterial deoxygenases. PhyH is a peroxisomal enzyme catalyzing the first step of phytanic acid alpha-oxidation. PhyH deficiency causes Refsum's disease (RD) which is an inherited neurological syndrome biochemically characterized by the accumulation of phytanic acid in plasma and tissues.	1.74078e-26
NZ_CP036292.1\|WP_145124074.1\|2264923_2267509_-\|heavy-metal-translocating-P-type-ATPase	gnl\|CDD\|319851	cd07553, P-type_ATPase_HM, P-type heavy metal-transporting ATPase; uncharacterized subfamily. Uncharacterized subfamily of the heavy metal-transporting ATPases (Type IB ATPases) which transport heavy metal ions (Cu(+), Cu(2+), Zn(2+), Cd(2+), Co(2+), etc.) across biological membranes. The characteristic N-terminal heavy metal associated (HMA) domain of this group is essential for the binding of metal ions. This subclass of P-type ATPase is also referred to as CPx-type ATPases because their amino acid sequences contain a characteristic CPC or CPH motif associated with a stretch of hydrophobic amino acids and N-terminal ion-binding sequences. This subfamily belongs to the P-type ATPases, 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_CP036292.1\|WP_145124071.1\|2254185_2255352_-\|AMP-nucleosidase	gnl\|CDD\|350162	cd17762, AMN, AMP nucleosidase. AMP nucleosidase (AMN) catalyzes the hydrolysis of AMP to ribose 5-phosphate and adenine. It is a prokaryotic enzyme which plays a role in purine nucleoside salvage and intracellular AMP level regulation. AMN is active as a homohexamer; each monomer is comprised of a catalytic domain and a putative regulatory domain. This model represents the catalytic domain. AMN belongs to the nucleoside phosphorylase-I (NP-I) family, whose members accept a range of purine nucleosides as well as the pyrimidine nucleoside uridine. The NP-1 family includes phosphorolytic nucleosidases, such as purine nucleoside phosphorylase (PNPs, EC. 2.4.2.1), uridine phosphorylase (UP, EC 2.4.2.3), and 5'-deoxy-5'-methylthioadenosine phosphorylase (MTAP, EC 2.4.2.28), and hydrolytic nucleosidases, such as AMP nucleosidase (AMN, EC 3.2.2.4), and 5'-methylthioadenosine/S-adenosylhomocysteine (MTA/SAH) nucleosidase (MTAN, EC 3.2.2.16). The NP-I family is distinct from nucleoside phosphorylase-II, which belongs to a different structural family.	1.44166e-115
NZ_CP036292.1\|WP_145119417.1\|2248937_2249816_+\|c-type-cytochrome	gnl\|CDD\|225797	COG3258, COG3258, Cytochrome c [Energy production and conversion].	3.37071e-56
NZ_CP036292.1\|WP_145119419.1\|2249799_2250429_+\|DUF3124-domain-containing-protein	gnl\|CDD\|378638	pfam11322, DUF3124, Protein of unknown function (DUF3124). This bacterial family of proteins has no known function.	4.35114e-64
NZ_CP036292.1\|WP_145119423.1\|2253268_2254177_-\|hypothetical-protein	gnl\|CDD\|320024	cd16226, EFh_CREC_Calumenin_like, EF-hand, calcium binding motif, found in calumenin, reticulocalbin-1 (RCN-1), reticulocalbin-3 (RCN-3), and similar proteins. The family corresponds to a group of six EF-hand Ca2+-binding proteins, including calumenin (also known as crocalbin or CBP-50), reticulocalbin-1 (RCN-1), reticulocalbin-3 (RCN-3), and similar proteins. Calumenin is an endo/sarcoplasmic reticulum (ER/SR) resident low-affinity Ca2+-binding protein that contains six EF-hand domains and a C-terminal SR retention signal His-Asp-Glu-Phe (HDEF) tetrapeptide. It functions as a novel regulator of SERCA2, and its expressional changes are tightly coupled with Ca2+-cycling of cardiomyocytes. It is also broadly involved in haemostasis and in the pathophysiology of thrombosis. Moreover, the extracellular calumenin acts as a suppressor of cell migration and tumor metastasis. RCN-1 is an endoplasmic reticulum resident Ca2+-binding protein with a carboxyl-terminal His-Asp-Glu-Leu (HDEL) tetrapeptide signal. It acts as a potential negative regulator of B-RAF activation and can negatively modulate cardiomyocyte hypertrophy by inhibition of the mitogen-activated protein kinase signalling cascade. It also plays a key role in the development of doxorubicin-associated resistance. RCN-3 is a putative six EF-hand Ca2+-binding protein that contains five RXXR (X is any amino acid) motifs and a C-terminal ER retrieval signal HDEL tetrapeptide. The RXXR motif represents the target sequence of subtilisin-like proprotein convertases (SPCs). RCN-3 is specifically bound to the paired basic amino-acid-cleaving enzyme-4 (PACE4) precursor protein and plays an important role in the biosynthesis of PACE4.	2.33077e-07
NZ_CP036292.1\|WP_145119441.1\|2270932_2271685_+\|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein	gnl\|CDD\|336781	pfam07722, Peptidase_C26, Peptidase C26. These peptidases have gamma-glutamyl hydrolase activity; that is they catalyze the cleavage of the gamma-glutamyl bond in poly-gamma-glutamyl substrates. They are structurally related to pfam00117, but contain extensions in four loops and at the C-terminus.	1.07514e-78
NZ_CP036292.1\|WP_145124072.1\|2255449_2256268_-\|heme-dependent-peroxidase	gnl\|CDD\|237033	PRK12276, PRK12276, putative heme peroxidase; Provisional.	7.10569e-103
NZ_CP036292.1\|WP_145124073.1\|2257567_2259028_-\|hypothetical-protein	gnl\|CDD\|368090	pfam04734, Ceramidase_alk, Neutral/alkaline non-lysosomal ceramidase, N-terminal. This family represents N-terminal domain of a group of neutral/alkaline ceramidases found in both bacteria and eukaryotes. The EC classification is EC:3.5.1.23. The enzyme hydrolyzes ceramide to generate sphingosine and fatty acid. The enzyme plays a regulatory role in a variety of physiological events in eukaryotes and also functions as an exotoxin in particular bacteria. This N-terminal domain carries two metal-binding sites, the first for Zn2+ residing within the domain, and the second, for Mg2+/Ca2+ lying at the interface between the two domains.	1.22729e-06
NZ_CP036292.1\|WP_145119435.1\|2264714_2264927_-\|cbb3-type-cytochrome-oxidase-assembly-protein-CcoS	gnl\|CDD\|377073	pfam03597, FixS, Cytochrome oxidase maturation protein cbb3-type.	4.37654e-15
NZ_CP036292.1\|WP_145124070.1\|2251319_2252699_-\|hypothetical-protein	gnl\|CDD\|238362	cd00688, ISOPREN_C2_like, This group contains class II terpene cyclases, protein prenyltransferases beta subunit, two broadly specific proteinase inhibitors alpha2-macroglobulin (alpha (2)-M) and pregnancy zone protein (PZP) and, the C3 C4 and C5 components of vertebrate complement. Class II terpene cyclases include squalene cyclase (SQCY) and 2,3-oxidosqualene cyclase (OSQCY), these integral membrane proteins catalyze a cationic cyclization cascade converting linear triterpenes to fused ring compounds. The protein prenyltransferases include protein farnesyltransferase (FTase) and geranylgeranyltransferase types I and II (GGTase-I and GGTase-II) which catalyze the carboxyl-terminal lipidation of Ras, Rab, and several other cellular signal transduction proteins, facilitating membrane associations and specific protein-protein interactions. Alpha (2)-M is a major carrier protein in serum and involved in the immobilization and entrapment of proteases. PZP is a pregnancy associated protein. Alpha (2)-M and PZP are known to bind to and, may modulate, the activity of placental protein-14 in T-cell growth and cytokine production thereby protecting the allogeneic fetus from attack by the maternal immune system.	1.71978e-12
NZ_CP036292.1\|WP_145119445.1\|2273011_2274373_-\|ribosome-biogenesis-GTPase-Der	gnl\|CDD\|274667	TIGR03594, GTPase_EngA, ribosome-associated GTPase EngA. EngA (YfgK, Der) is a ribosome-associated essential GTPase with a duplication of its GTP-binding domain. It is broadly to universally distributed among bacteria. It appears to function in ribosome biogenesis or stability. [Protein synthesis, Other].	0
NZ_CP036292.1\|WP_145119437.1\|2267589_2269047_-\|anthranilate-synthase-component-I-family-protein	gnl\|CDD\|223225	COG0147, TrpE, Anthranilate/para-aminobenzoate synthases component I [Amino acid transport and metabolism / Coenzyme metabolism].	3.60148e-140
NZ_CP036292.1\|WP_145119433.1\|2263323_2264700_-\|c-type-cytochrome	gnl\|CDD\|365823	pfam00034, Cytochrom_C, Cytochrome c. The Pfam entry does not include all Prosite members. The cytochrome 556 and cytochrome c' families are not included. All these are now in a new clan together. The C-terminus of DUF989, pfam06181, has now been merged into this family.	5.4341e-09

>NZ_CP036292.1|WP_145124073.1|2257567_2259028_-|hypothetical-protein
MYSAAELRAAELTAGVAKVDITDMQAGPVNDRSYVRALVISDGTTTAAIVTVDAVAIGEIGRIDNEYLGKVRGEVEKSLGISPANVMINASHCHSVVRTDVDELTVQAISQAAAKMVPVQVGVGVGHEDRIMENRRLQLADGRQIDVRHAYSLPPDEAVAAVGPIDPQIGVLRVDTTEGDTLAIVYNFACHPIQGVPGGANTADMTGYASDVIEQNMSDGTVALFVQGCAGDINPIDYKDVDHPRHAQTLGNLLGLSTLQAARKIETRPDATLRVVNETLPLPRADLAQRIIEMEAEREKLVNSLTGTSLNLKTFLPLVVKYRLSEEFPSYYSHRYLHDKALGRSDLRHLDIENRKNMARYIDNIHTMEQITRVNTNIRLLRKHQADLVDGGKRMIDVELVGLRVGDFVLTTFPGELTVQIGKNIKQASPHEHTFVAGYTNGYIYYAPTADQLRNVGNAQEDSDCVLAPAWQALYEAKAAQILSKL
>NZ_CP036292.1|WP_145119425.1|2256466_2257552_-|hypothetical-protein
MHLDTNRSLLGDLHLAPPPTGPRSTSDREVPASEVRRAHGPAIPLRCPLFAYDLPWALLPPTTCALLAHELTESAVVTSLLDLDVDEDRPADLVMCPYRPERYGVTIDDLSRAAFVDLRLNSEVGDGSVYTMDQLRRWDHRADSLPDSTVITGSRWPADVALPDKLGRKIEQLRALAPQAAIFVAISPFHLQQDLPNLLAARPDGIVLRFDLDPTSPSVGNLIAAQTAACRRMIDASEAAGIALWVSAPTTSPLDLVKLLALGASAVSIDYLVLHNWPAADPAPAAGDPHASYAHASALGPPSTGTATATRMISPIIDTLLNEALTYVHGLGVAHYSQLRPHMLACIDPTLAKRTGAMLVE
>NZ_CP036292.1|WP_145124072.1|2255449_2256268_-|heme-dependent-peroxidase
MPEPSRTPSEGLHCSHFMYRFRRDVLAGLSARRLRDGMRQFLAAVDPAEATRPEKLQRYIISGHKADFALMMMDADPLKIDAVHQAVVSGPLGAAVEATWSFVSMSEISEYVPSVPQYREKLIREGNAPDSPELAAKVAAYERRLPMMNQQRLSPDIPDWPAACFYPMNKSRVPGANWFMESSSLRQSLMAEHAQSGMAFAGRVSQLITVGVGLDDWEWMVTLWGRNPEHLKEIVYRMRFDQASAKYGEFGPFYVGYSATGEEILDHCRINV
>NZ_CP036292.1|WP_145124071.1|2254185_2255352_-|AMP-nucleosidase
MQILPGQSQADLEQQIEAACALMERHYASGVYSKLTVVRSWSKHNPTISGSIARPSAFRWYLRRELTKLAQRGAQLHVAPSRARVDLNAPKLLQLIDESDFDHTRKKVFLFGPERAELSIQRLEHYTGTQVEDFQRYVLLTNYQMHMNAFIEAYPDCIRPQRTDVQMPALHQRTVNNDGVTIINIGVGPSNAKNLTDHIAVLRPDAMLMVGHCAGIRNHQEIGDFVLGSGYMRADRLLDQTLPTSVPLSPNFVLNRNLARVLDERKLPYRFGVVYTTIDRNWELTLRGTLADLRASRSIAVDMESATVAANGFRYRIPSATLLCVSDKPLHGKPKLAAEALEFYKKTKSQHLAVAIAAIELAKQEFPGGFPNSDIRAMDEPLLGGPET
>NZ_CP036292.1|WP_145119423.1|2253268_2254177_-|hypothetical-protein
MSESDRVKKGFRRRKRENQSPRFMRNVCLPLGFHSTCRRWSDPRSRSESSAPVRSLLEIQPRVKKMRYRHFAATAALLVSVGVSAGIAVAQDGPGDGDRPRPRDGGPRDGGPRDRGPRHGAPRLPPIPILEALDSNGDGMLDATEIEQAAKALKSLDRDNDGKLSFQEMMPAPRGDRGPGGPQGRGDRPEMRDGQGRPDGEGRRPRPEGEGNRRGGNPEQFVERILKLDKDGDGKLSGEELPERMRAMLSRADVDGDEALSKEELMKMAERRGRQGGGEGRRRPDGEKPTEGGERPRRPPAE
>NZ_CP036292.1|WP_145124070.1|2251319_2252699_-|hypothetical-protein
MFLHLSLLLALAFITLAASGGDRALLTLRQGEWEPQAELAEFVIEPIAPLELPIEAVAEVQHDPEFDLRSLQVDQPTVETVAMASSSPMLDQLIAKTTPSADLTTPIRTAHPAMFAGRSGPLKAELLKKYGGTKLTEDSVALGLAWLKRQQLPGGNWSMRGPYTTGSFSENETAATAMAMLAFMGAGSTHRSGPYEKEVLRAVHWLAKQQDRSGFMAHRANSHEKMYAQSQAMIALCELYAMTKDSWLRPYAQAACDFADKSQSPAGGWRYQPRTDSDTSVTGWFLMGLKSGQTAGLEVDPDVLLRVGKFLDTVGGGYDEGYAYMQGERSSPTMTAVGLLCRQYLGWQRNHPAMSRGLITLEANYPIDPGQPDVYYWYYATQAMHHYGGPLWDDWNAKLRVDLPAMQDKQGAERGSWPPQRDAWGRLGGRLYTTCFSLYNLEVYYRHMPLYSQDQTDVW
>NZ_CP036292.1|WP_145119421.1|2250553_2251261_-|hypothetical-protein
MSHQQHRLICAAFAILVSAAASPAFAQSGTIPISELPTPPAQIADLIDRGNVRFVYGWDARPDAKLPDVGRRLDGLTVYELSYQFEHHTSLRNRNSSPHAVTRIRLSESGLRCKHTVWFREAPQIETFWSNPLVLHELDHVLISSDPRLASLFLTQVQDQPLITPIEGSSYSSAVAAEVNRVAKEHVATIYLSILSLVDIRYRELDRVTNHGARPLPAELQLRLSNSQPTAPQGQ
>NZ_CP036292.1|WP_145119419.1|2249799_2250429_+|DUF3124-domain-containing-protein
MKDITEKAAGKMVRQIKLIVFLTVVLPIVALAIFVELRFASIKDDLHFREPGARDEARMDLDSLPWSPIQGQTLYVPAYSHIYQQGGDPRLLTVTLSARNTDQAHEIVITSVRYYDTAGNELRSLVEKPLRLAPLASTEFVIEQKDKSGGSGASFILEWKAGKPVTHPVVESVMIDTNNAQGISFVRSATVLEETRPDNGNSESEQPES
>NZ_CP036292.1|WP_145119417.1|2248937_2249816_+|c-type-cytochrome
MRDKELPAMRWFGWMCVPLMVVSIAIGDEAGDRSANHAADAAKHASGPRQLPPGELGRVIKLGREIVLNTSEHPLSKPYVGNALNCTSCHLDGGEHPQAASFLGIATAYPAWSPREQRVVTLQDRSLNCFMRSQNGTRPPLGSEVSVAITAYITWLSTDQPIRQNPNKPLGPRHVPALDAPDQQPSVSRGAVLYADHCASCHADNGLGSDDGPPVWGDESYNDGAGLSRVPKLASWLKVAMPLDDPYLSTAEAFDIAAFVNSHRRPHFELSKHLPAADARGEYNGVSDEGHH
>NZ_CP036292.1|WP_145119415.1|2247312_2248587_-|hypothetical-protein
MTSLASYPAEIAAALQRRWTAMELPADALPAADAVAQLVDTMYQASLLREEGSGVRCRIIVAPPSEFAAELSTGASQLHVLRFTERRDFTPHQLRKLAAAAGYYRALLAVDQNADGQLSIWGMVITGTDWVNRVEGERVRELWLPTRPVIHCVGPGHLIAAAGYSRILESSGGKLLTDGFDPFRSSWLSHQFRQVRTSLIEELAELETDSSKTRMCDSFVKDIAQSVVRRVLHLVRTRGHGGMLVFLPNGLESNPLVDRWFRFRVRFEGDDSTLRFRRLILNLMQQGRRAGEARGLDQVTWDDYLQMRHAELAQLDAALLEFGHFLADLMSADGSLVVDRSFRLVGFGAEILGDSHVNTIHRAFDLEAINAVPEPADSSGTRHRSAYRLVSGLREAIAVVVSQDGDVRFVAHHKDKLTYWPYLP
>NZ_CP036292.1|WP_145119429.1|2259907_2260399_+|hypothetical-protein
MDTQLLIDTLSRVIHVATAITLVGGSAFMLLVLIPAALNLSDEEHDRLRTGLIARWKRFVHIGVTLFLISGLYNYYRAIPSHKGDGLYHALLGTKMLIALVIFFIAAALVGRSAKLEPIRRKRTLWLKVLLICALIVVTISGFVKVRGPQPPAAAKAPAAVTE
>NZ_CP036292.1|WP_145119431.1|2260472_2263160_-|hypothetical-protein
MHHAKLFLYLVGLSYCLSNPWFPTTAVGQEVIAIAGETYGVGYARVQWPQPVEGLSRVLVTSPQGRVLYPTAEPVTVTVRDPMRLDPAPRELKFGRGKILERLGQVVKAAVTADEREQVTGYEIWFLFQGDSPFELQISGPAVATIPIVPVAASPEDQRAAMLQWWQTYQDQAEGQIEAAPFLPVADAYLLSYLSRRLDLPAPASLSRMRLEKPPAAIAMMADSAVLQRIALANVLRGNSTEESEVLTDLPAAAAPPEIDPLDDDDVPAEIEPIARMVPPECFYLRFGSFSNFLWFQKLAQEHDGDIKNMVARPILDRRSSQRIEELLNVRYNQLADLFGDALIGDVAVIGNDLLIDDGPSIGVLLQAKNAFLLSTFLEKDRRATEAQFDDCTLETKTIEGIEVSLLSTPDNRVRSFWISNGNWMFVTSSEHLAGRFIAARKSRTTLAATAEFQQFRKQYPNAKTAAITFYLSGRFLSRLYTPQFQIELQRRSHAAAEMAVLVAARATAANEGKTLELPEDLIAAGYLPEGFGRRADRSGLILTPDGMLDSRRGGRQTLLPIDDTTIDKITPAERVWQDQINRSRTDQPGLLEPVFIQIARATADSKSPGQERLQIALDISPGLLGKQAWLVDQLGPATDIGVQFSKSDLVSFYANVHSDKLNGSIPPHYLFGGIKDCRPAPLEKFESPIDRIFAFSTIRGYLAAWPDPGLIDRLPLGLGRGSPVGPNMTRLVGGAYRYQSERVSLLSFNREVLVESIPDLAVLDKQPLRRAQLTIADLSQTDLGQWVSETLLEGEQKKSQAGCDLLSRLTEQLGIDAASTLPFAEELLGAAMQCPLHGEYHCRDDGHWCSSATEAHAPQTAAVMNWFRGLEASVDVVDERLLIDMEVDVKRAAK
>NZ_CP036292.1|WP_145119433.1|2263323_2264700_-|c-type-cytochrome
MPTSPRRIGMANDTIQQTTTLHRITMKTTTYALLLIGLAALTGCEKPYVAEFEPNMVLAELVSMSVEEPMDQALAETQTALTRLFGTPDDPKLPDFLLEDPDLGTLVSMDNLVAASGSPSEQGRGLYRQHCSTCHGITGNGRGTTAALLDPYPRDYRMGKYKFKSTRRGSKPLREDLHFAITHGLDGTAMVAIPELNKNPEDVEALIDYVMYLTWRGEVERALLEEAELIDFAAGETLFDNAMVDKYLQKYKDDFDPETLTDEAQIEEYEMFAEQWEFIQDLTFGAVEGWLDAEDAVVEVPEPEDVPVPATIDEVVAAAKAPGDSPLKQSIQRGKELFVTERAACAKCHGPKGWGDGTNKDYDDWTKDWTLQRGIDPTDEAAQIPLIARGVLPPRLIKARDFRQGLYRGGSDPELLYLRIAAGIDGTPMPAASLEPNQIWDLVNYIRSLREDAPMSIQ
>NZ_CP036292.1|WP_145119435.1|2264714_2264927_-|cbb3-type-cytochrome-oxidase-assembly-protein-CcoS
MSVLFVALPLALALGAAGMIACVYCIRGGQYDDLETPAVRILIDDRDTRPQPAKAAESDLDRRGSADPDG
>NZ_CP036292.1|WP_145124074.1|2264923_2267509_-|heavy-metal-translocating-P-type-ATPase
MPADEAASADETACPAIVELPCVHCGLPTRVRADADPQRIFCCNGCHGAYDLINGWGLSDFYALRDQMTSAAAQGVPGQRSRYDVFDQPEFLGDSAPKPQSGGLLSTDLALHGLHCGACAWLIENAAARIDGWQLARVKMSDHTIRIVFDPQRVPLSEIARTMDRLGYQVAPLTKQLDDHFARENRRLLIQIAIAGFCAANAMWIAIGLYAGEASGVDADHRTFLRTIGTGLGLLAVAVPGRTFFRGALASLRTRTPHMDLPVALGLSVGSIAGLINAITGRGDVYFDSLAVLVFFLLIGRWIQFRQQHRAARSVDLLLRITPRHASRILDDGETQAVLADNLQAGDRIRVAAGESFPADGEIIAGETTIDRSLLTGESQPIRAAVGETVLAGTVNVTRSIDVCVEASGDASRIGRVMQAVEAAAARKTPIVQLADRIGGIFVIVVTTLALVAFALSARDNWQQGAANATALLIVACPCALALATPLAIAVSLGRAARRKILIRDGSSLQQLAGTGTIWFDKTGTLTEGRSRVVEVIGDRDGLASAAAIERDVCHPIADAILAAADLPDDLEGVAATDKDNSPAGTDSTDEATARTQIAIGGVLGEHRGAAIAAGSLKFIQSQGIEIPAKLSQAAERLTAQGTTAIVVARDAIAITVLGIDDPLRAGADVAIAELKRAGWRVGILSGDHPGVVRSVADRVGVPQSLAIGGLSPENKLDIVSHHSPADPGSAELHLPEPAPGLQVMIGDGANDAAALAAADVGIAVRGGAEVSLQAAPIFIASGRLGSVVELVRGARRTARLIHITFAVSLGYNVIAVGLAMAGRISPLVAAVLMPLSSVSVLSLTLASRSFRERDELERTK
>NZ_CP036292.1|WP_145119437.1|2267589_2269047_-|anthranilate-synthase-component-I-family-protein
MVIPTPADLHPATPDFTSAGDCPLVAPLPPQTDLREVFLRLCHLPHCLWLDSAKPMPDLGRYSFLTADPIEIVSATDDDADPLAKLQKFIPLLSQAAAPGLPPFQGGLAGVLGYELGRSLEPIPAPRFNDLPTPPLCLGLYDWTIAVDHQQNRGWIISQGWPETDPDRRRVAAARRMQQIQWWLGCTPTAMPRPPRSAPRAHDALAPQFRTPIDASLTSNFAPGEFRTAVGDVIDYIRRGDAFQVNLAQRLLYPDQHGAVAAYLRMRSRNAAPFAGYFDGGDWQVVSASPERFLQIDDRFVETRPIKGTCPRTGDAAVDQQLGAQLLSSLKDRAENVMIVDLMRNDLSRVCNDDSIDVAGLCELEQYECVQHLVSRVHGTLQDDVGVVDLLRASFPGGSITGAPKVRAMQIIAELEPTARGPYCGSLGYLSTGGRGDLNILIRTVTCRDGWLQMPVGGGITSRSKPVQEEQETWDKAEGMLRAVL
>NZ_CP036292.1|WP_145119439.1|2269103_2270225_-|3-oxoacyl-ACP-synthase-III
MQFENVCIESLGVHLPEEVWTSDEIERRLEPLYSRLRLPEGRLELMSSISQRRVWPAGTLPSGPSIESCKSAISAAGIDPARVGCLIHASVCRDFLEPATASRVHHGAGLSPNCWVYDVSNACLGLLNGIVQIATLIEQGAIEAGIVVGTENSRPLLEATINNLNTDESITRKTVKPAFASLTIGSGSCAVLLTHRRISQSGSRLEHAVSHAATDGHNLCRSDTDSAGANMAPLMDTDSERLLAAGVAAGAAGFEKLLADAKWDRADIDRTICHQVGGRHRALMLETLSLPPENDTAVFPWLGNTGSVALPLALAAAGQYQHVQPDQRIGLLGIGSGINCVMLGCKWQETRVAGNLPAVEPVMGQESLTAVEA
>NZ_CP036292.1|WP_145119441.1|2270932_2271685_+|gamma-glutamyl-gamma-aminobutyrate-hydrolase-family-protein
MTSTRPLIGINTDFRPAQQRTPAYVYLAAGYYENIQAAGGIPVILPPSDDVDAIHAAMDRLDGFVLIGGQDLDPRNDGYMLHHSMKLMHSNRETFDRIVVNEITERRMPVLGIGAGMQLLNIVQGGNLFYDIAEDLPNAVPHRDHQDPLHRHSLVVESDSLVGRVYGDGEIRVASRHHMAIDEVAPGFRVTARCPDGVIEAIESEMMDWFAVGTQFHPECEAASALDIRIFEEFVDGVKERQTGDLRLVA
>NZ_CP036292.1|WP_145119443.1|2271971_2272799_+|phytanoyl-CoA-dioxygenase-family-protein
MKNFSIVPTDDELASVPRDLRFYSVNNDAPTVLTGDQIDRFNRDGYVAPLPIFGDAEISGIRSYFDDLLARVTAAGGNSYSISSAHLKYGPVYDILKDPRIVDCVSDLLGENVIGWGSHFFCKMPHDGKSVAWHQDASYWPLSPSKAVTVWLAIDDADEENACMRFIAGSHHVGHLTYRPSDSAEHNVLNQTIDNPEQYGSVVYNPLPAGSASIHSDLLLHGSKANDSDRRRCALTLRYCSADVHAALDWNQKGVQVRGTDPSGHWSNLTRPAES
>NZ_CP036292.1|WP_145119445.1|2273011_2274373_-|ribosome-biogenesis-GTPase-Der
MSMPKVAIVGRPNVGKSSIFNWLAGRRIAIVDDYEGVTRDRMTTLIEHEGNFFELIDTGGMGVVDSDDLTADVEAQIEVAIATADVILFVVDIRTGLMPLDSLVAERLRSIDRPIVLLANKADHENLDISAEEFHKLGRGHLICVSAEQKRHRDELMQLIVDRLPPSSDRAVDAHMKFAIVGRRNVGKSTFVNSLAQAKRMIVSEVAGTTRDSVDVNFELDGHQFTAIDTPGLRRRRSVRTDLDYYGMHRAQRSIRRADVSLMFFDASEKISKVDKQLVGYIADEYKPCVFVVNKWDLYHDEMPTERWVKYLRSQFPTMQYAPIAFITGQTGKNIKALLNHSQMLFKQARERTSTGRLNRIVQAAIEHQEPPMFQNRRPKIYYATQVSTEPPTIVLMCNDPKGFAPDYRRFLLSVLRDNLPFSEVPIKMYLQKREQRDPTAPPEVDQENERVS

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Crispr_ID: NZ_CP036292_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_12

2859696-2859820

Orphan

Consensus_repeat	Method
CGCCATTTCAAGTCCCCAGTCGCAACGCGACGTCATGCGTTAGCCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_12

>merge|NZ_CP036292|12|2859696-2859820|CRISPRCasFinder
CGCCATTTCAAGTCCCCAGTCGCAACGCGACGTCATGCGTTAGCCTGGGACGCAAGTCCCAGGAAATCGCCCTCCATCGCGCCATTTCAAGTCCCCAGTCGCAACGCGACGTCATGCGTTAGCCT

>NZ_CP036292|12|12|2859696-2859820|CRISPRCasFinder
CGCCATTTCAAGTCCCCAGTCGCAACGCGACGTCATGCGTTAGCCT	GGGACGCAAGTCCCAGGAAATCGCCCTCCATCG
CGCCATTTCAAGTCCCCAGTCGCAACGCGACGTCATGCGTTAGCCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145120189.1\|2847771_2848830_-\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|366359
NZ_CP036292.1\|WP_145120195.1\|2851502_2852993_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369347
NZ_CP036292.1\|WP_145124102.1\|2868508_2869732_-\|acetylxylan-esterase	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120211.1\|2865016_2866255_-\|acetylxylan-esterase	unknown	unknown	gnl\|CDD\|224423
NZ_CP036292.1\|WP_145120191.1\|2849139_2850711_+\|YdiU-family-protein	unknown	unknown	gnl\|CDD\|234583
NZ_CP036292.1\|WP_145120187.1\|2846718_2847624_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223021
NZ_CP036292.1\|WP_145120205.1\|2860375_2861539_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|379188
NZ_CP036292.1\|WP_145120217.1\|2870566_2871463_+\|ThuA-domain-containing-protein	unknown	unknown	gnl\|CDD\|377643
NZ_CP036292.1\|WP_145124101.1\|2862966_2863941_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133030
NZ_CP036292.1\|WP_145120185.1\|2846203_2846467_+\|DNA-directed-RNA-polymerase-subunit-omega	unknown	unknown	gnl\|CDD\|376482
NZ_CP036292.1\|WP_145120193.1\|2850735_2851245_-\|peptide-methionine-(S)-S-oxide-reductase-MsrA	unknown	unknown	gnl\|CDD\|237597
NZ_CP036292.1\|WP_145120203.1\|2859986_2860265_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120201.1\|2857668_2859321_+\|ribonuclease-Y	unknown	unknown	gnl\|CDD\|188306
NZ_CP036292.1\|WP_145120207.1\|2861798_2862821_-\|molybdopterin-biosynthesis-protein-MoeB	unknown	unknown	gnl\|CDD\|181084
NZ_CP036292.1\|WP_145120183.1\|2845616_2846219_+\|guanylate-kinase	unknown	unknown	gnl\|CDD\|213788
NZ_CP036292.1\|WP_145120213.1\|2866767_2868132_-\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP036292.1\|WP_145120197.1\|2853269_2855216_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224001
NZ_CP036292.1\|WP_145120215.1\|2870002_2870359_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120209.1\|2863946_2864906_-\|putative-2-dehydropantoate-2-reductase	unknown	unknown	gnl\|CDD\|180488
NZ_CP036292.1\|WP_145120199.1\|2855320_2856565_-\|outer-membrane-beta-barrel-protein	unknown	unknown	gnl\|CDD\|369446

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145120189.1\|2847771_2848830_-\|methyltransferase-domain-containing-protein	gnl\|CDD\|366359	pfam00891, Methyltransf_2, O-methyltransferase. This family includes a range of O-methyltransferases. These enzymes utilize S-adenosyl methionine.	3.92904e-26
NZ_CP036292.1\|WP_145120195.1\|2851502_2852993_-\|hypothetical-protein	gnl\|CDD\|369347	pfam07396, Porin_O_P, Phosphate-selective porin O and P. This family represents a conserved region approximately 400 residues long within the bacterial phosphate-selective porins O and P. These are anion-specific porins, the binding site of which has a higher affinity for phosphate than chloride ions. Porin O has a higher affinity for polyphosphates, while porin P has a higher affinity for orthophosphate. In P. aeruginosa, porin O was found to be expressed only under phosphate-starvation conditions during the stationary growth phase.	0.00672896
NZ_CP036292.1\|WP_145120211.1\|2865016_2866255_-\|acetylxylan-esterase	gnl\|CDD\|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	0.0062078
NZ_CP036292.1\|WP_145120205.1\|2860375_2861539_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|379188	pfam13443, HTH_26, Cro/C1-type HTH DNA-binding domain. This is a helix-turn-helix domain that probably binds to DNA.	2.5321e-06
NZ_CP036292.1\|WP_145120187.1\|2846718_2847624_-\|hypothetical-protein	gnl\|CDD\|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	0.00216459
NZ_CP036292.1\|WP_145120191.1\|2849139_2850711_+\|YdiU-family-protein	gnl\|CDD\|234583	PRK00029, PRK00029, YdiU family protein.	0
NZ_CP036292.1\|WP_145120217.1\|2870566_2871463_+\|ThuA-domain-containing-protein	gnl\|CDD\|377643	pfam06283, ThuA, Trehalose utilisation. This family consists of several bacterial ThuA like proteins. ThuA appears to be involved in utilisation of trehalose. The thuA and thuB genes form part of the trehalose/sucrose transport operon thuEFGKAB, which is located on the pSymB megaplasmid. The thuA and thuB genes are induced in vitro by trehalose but not by sucrose and the extent of its induction depends on the concentration of trehalose available in the medium.	2.1561e-40
NZ_CP036292.1\|WP_145124101.1\|2862966_2863941_+\|glycosyltransferase	gnl\|CDD\|133030	cd04187, DPM1_like_bac, Bacterial DPM1_like enzymes are related to eukaryotic DPM1. A family of bacterial enzymes related to eukaryotic DPM1; Although the mechanism of eukaryotic enzyme is well studied, the mechanism of the bacterial enzymes is not well understood. The eukaryotic DPM1 is the catalytic subunit of eukaryotic Dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. The enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. This protein family belongs to Glycosyltransferase 2 superfamily.	5.61637e-79
NZ_CP036292.1\|WP_145120185.1\|2846203_2846467_+\|DNA-directed-RNA-polymerase-subunit-omega	gnl\|CDD\|376482	pfam01192, RNA_pol_Rpb6, RNA polymerase Rpb6. Rpb6 is an essential subunit in the eukaryotic polymerases Pol I, II and III. This family also contains the bacterial equivalent to Rpb6, the omega subunit. Rpb6 and omega are structurally conserved and both function in polymerase assembly.	3.30933e-09
NZ_CP036292.1\|WP_145120193.1\|2850735_2851245_-\|peptide-methionine-(S)-S-oxide-reductase-MsrA	gnl\|CDD\|237597	PRK14054, PRK14054, peptide-methionine (S)-S-oxide reductase.	1.22384e-112
NZ_CP036292.1\|WP_145120201.1\|2857668_2859321_+\|ribonuclease-Y	gnl\|CDD\|188306	TIGR03319, RNase_Y, ribonuclease Y. Members of this family are RNase Y, an endoribonuclease. The member from Bacillus subtilis, YmdA, has been shown to be involved in turnover of yitJ riboswitch. [Transcription, Degradation of RNA].	0
NZ_CP036292.1\|WP_145120207.1\|2861798_2862821_-\|molybdopterin-biosynthesis-protein-MoeB	gnl\|CDD\|181084	PRK07688, PRK07688, thiamine/molybdopterin biosynthesis ThiF/MoeB-like protein; Validated.	6.98605e-130
NZ_CP036292.1\|WP_145120183.1\|2845616_2846219_+\|guanylate-kinase	gnl\|CDD\|213788	TIGR03263, Guanylate_kinase, guanylate kinase. Members of this family are the enzyme guanylate kinase, also called GMP kinase. This enzyme transfers a phosphate from ATP to GMP, yielding ADP and GDP. [Purines, pyrimidines, nucleosides, and nucleotides, Nucleotide and nucleoside interconversions].	6.89682e-80
NZ_CP036292.1\|WP_145120213.1\|2866767_2868132_-\|IS4-family-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.	0.000673358
NZ_CP036292.1\|WP_145120197.1\|2853269_2855216_+\|hypothetical-protein	gnl\|CDD\|224001	COG1075, LipA, Predicted acetyltransferases and hydrolases with the alpha/beta hydrolase fold [General function prediction only].	8.02557e-05
NZ_CP036292.1\|WP_145120209.1\|2863946_2864906_-\|putative-2-dehydropantoate-2-reductase	gnl\|CDD\|180488	PRK06249, PRK06249, putative 2-dehydropantoate 2-reductase.	3.08351e-159
NZ_CP036292.1\|WP_145120199.1\|2855320_2856565_-\|outer-membrane-beta-barrel-protein	gnl\|CDD\|369446	pfam07642, BBP2, Putative beta-barrel porin-2, OmpL-like. bbp2. BBP2 is a family of putative porin proteins that are likely to be outer membrane beta barrel proteins porins.	5.77568e-64

>NZ_CP036292.1|WP_145120201.1|2857668_2859321_+|ribonuclease-Y
MNALDNILGLQLHLLATVDKDSASEFGLWLVSTSTLILLALAGALFGFCSNWLYQRTLDKRGIRQAKLDSEAMIEKAKLETESIHKNAALEAKEIVIRHKAEADEEISRVKESLRETRHELESRAATLAQSEEGLKKQERGLENTQRRLAQQLEAVNRKRERLDQLTDEKQKILQQASGMSKEEASKQLMQTLQMELDQEIGTAILHHERHLSESLDAKAREMLLTAMQRYAAVHTAENTTSTVDIPNDDMKGRIIGREGRNIRAFEKATGIDVIIDDSPGVVIVSGFDPVRRELARQSLDKLISDGRIHPSRIEEVVAQTSKDLDEFIRRKGEEAADEVNVPGLNKRIIEMLGRLHFRTSYSQNVLRHSIEVAYFSSMIAEMIGLDPDVARRCGLLHDIGKAADHELEGGHPKIGADLLKRHNESPEVVHAAFGHHDEIITEFPYTVLVATADACSASRPGARRESLERYVKRMEELESIATDFDGVEQAFAIQAGRELRVIANSKITDDAKAAAICRNIAKAFEQQLTYPGEIKVTVVRESRFTELAR
>NZ_CP036292.1|WP_145120199.1|2855320_2856565_-|outer-membrane-beta-barrel-protein
MLRSTVGLWSLSIAVMFIAAARQPAAAAECTPVTADCDALQCDTDTVAQTGSLASLLNDCRETSGVAMGGWISTGLTLNGDGNRSGTGNAPYGYNNVSDGVVVNQIWMFAERQIADDGLDWGFRIDALFGTDGPDNQAFADQTWDFGWDSGRDYGAAIPQMYADVRIDDLAIRAGYFLTPIGWESVPAPLNFFYSHSYTFYYSEPNTHSGFLATYDVNDRLTLSGGWTMGMDSSFANDLHASTFLGGATLAISEQTTLTWSLLAGDWGDGTGHDGVPSDEGDIYIHSLILEHQVSDRCSYVLHNDLGANTNQATAPDAHWYAIVQYLMFEINDAWQAGTRVEWFRDDGGVRVGDSAADAGDYFELTLGLNWHHESQWIVRPEVRWDAAGGGLQPFDDGSEDDFFTYAVNAVRTF
>NZ_CP036292.1|WP_145120197.1|2853269_2855216_+|hypothetical-protein
MRKRLFPNLLCHAILLVAITGCGCMRSDRLRSPTLVSPSLAACSYEGWLGLGSLIAGQGKIDDFERYRLQASLHPTAESSTALGERAYAVAERLHGQCDHRAVDYWAQTIAWLDDGRRRCGVSGGKDPSDRIARVRHSALIRILSCGQKYGRLDPASHLTLHADAGPIQVPIVHDGFAWRQSDFQRLMVFESPASALGNVCGRGVPLIVFTSKKEGQHAASGCGDGCDTCCSTDPSTDNRCEKFLDSRLPFAATALLDLPVSLFQNRAACDDAETDRFSAATMRLVNPLASDLPETYAGIAKSPAMPLYYARQSSQYNPVVAFIGGDNGIDRPELKFLEPYQPDKIPLILVHGLLSNPATFLEVADAVRADPQLASRYQIWVFRYPTGDEFLQSTAVMRQQLAAAFACHTGGSPDQRHPHRAVIVGHSLGGLLSKLQVTSSGDRLWRSIADVPLDQLRGTPQYIAHLRRSFFFEASPNIGRVVYIATPHRGSPWAARCIGRIGSSLAGYRSEDKRDFQQLAAANPGVFSGEFSDSLPSSVDLLRPNSQLLEALAATPSSPHVIVNSIIGDCFRLPRAGPSDRVVPVSSAYRKEAESTAYVDASHTAILRSSAAHAELLKILRRHLQETASGECRCRLERPEIELAPAI
>NZ_CP036292.1|WP_145120195.1|2851502_2852993_-|hypothetical-protein
MPMDSIVPYRPLLTLDPDVRFLPVIASIVALIVSQDSVPAIGQESMIASNAVVPASYDAAAAGTPPAADQICDIADPHSPWTPGDGVSASAQLRRFSDSIRVGYDDGFVIASLRERDLEAEAFPFRLKVNGWGQLRHTASDVALPNTDLNQFQMKRARLILSGNAFLPDLTYFTQFDGRSSSGDDMRLLDFYLSYDIGHSQFGFEKGTFGFRAGKYKMPFTMARWLSGKEFEFSDRSVASTYFDVNRSLAVGLFGESKHTAIPIEWETAIFNGFVTGGAETGSSGNLDDNFAYSIRLQGYPIGDWGDSQLADFESHDRLAMRVGCAFAGTTISRNGSTEFNTPRVVDSGQTFASILPLAVDSYHVSQFALDASFKWRGWSSTMEYYFRNLSDFEGPGIPSLLDHGFWFQLGFFVVPEKLQVLTRWSRVDGDSGTLGASDQSTDEVGAGLAWYLRGNRAKIVTDVTRLDGAPINSSALDVNPGDRGWLYRTQMQFSF
>NZ_CP036292.1|WP_145120193.1|2850735_2851245_-|peptide-methionine-(S)-S-oxide-reductase-MsrA
MNERAVLAGGCFWGMEDLFRKQPGVVATRVGYTGGDVPNATYRNHGQHAEAIEVIFDPSQTNFRKLLEFFFQVHDPTTPNRQGNDIGSSYRSAIYYTNDDQKRVAIETIADVDASGIWPGQVVTEVEPAGDFWEAEPEHQDYLLRNPNGYTCHFLRPDWVLPQRPEASQ
>NZ_CP036292.1|WP_145120191.1|2849139_2850711_+|YdiU-family-protein
MQLQIDDHFIHALPSDPDRSNQRRQVRGAAYSFVTPRVPSQPTLLHAAADVAAMIGLSEEDLKAKRFTDVFSGAVVPEGADPYAMCYGGHQFGNWAGQLGDGRAINLAEVSHEGVRHTLQLKGAGETPYSRMADGLAVLRSSLREHLCSEAMFHLGVATTRSLSLIATGDAVLRDVMYDGHPEYEPGAVVCRVAPSFIRFGSFEILASRGEIDLLRQLADYTIGHYFPTLDADAPDYIEFFREVSQRTMAMIVDWQRVGFVHGVMNTDNMSIHGVTIDYGPYGWLEGYDHGWTPNTTDRQHRRYRYGNQPQIALWNLAQLASAISPLVDDVQPLRDVLEDFQQEFPKRYFEMMAAKIGLDRFQAGDEALCNDLEDVLQLTETDMTIFFRRLASIPSDLDLQRGVEFLQPVADAFYDPAQVTGEVLERWRSWFTSYTERLRQSEETQPDRMARMNSVNPKYVLRNYMAQMAIDKATQGDLSLIDELYDLLRDPYAEQPDRETWFAKRPDWARDKVGCSMLSCSS
>NZ_CP036292.1|WP_145120189.1|2847771_2848830_-|methyltransferase-domain-containing-protein
MTHNALRFPETDPTPIFEHFRGNQGSDLLTAAVAHFDLFGSLDRQPCSFDELAQRLGLAARPANVLVTALRAMKLLELREGRLELTPLAREHLVPGSDFDCGDYLGLAAQTPSVLQMVSLLKSNRPIGADASDGDGAAFIYRDGIASAMEAADTARHFTLALSGRAKNVAPALAEVADLTGARQLLDIGGGTGIYSYALLQKHPALQAILLDRPEVLHVAEEVGQRYGVLDRCKFVGGDMFADPLPADVDAILLSNILHDWDLPECQNLIGRCAAALAPGGRLMIHDVFLNDALDGPLPIALYSASLFSLTEGRAYSGGEYRGWMEAAGLKCSETIATTGVHCGLLIATKPA
>NZ_CP036292.1|WP_145120187.1|2846718_2847624_-|hypothetical-protein
MRATLTYASIACLAIHGLAIELHANERPSKNPLVKAWHAVGRTYGVGHGPGYHACPNCNGVCNCGRSGGTMHYGTAGHHGTPTTYSYDGTTQSLPAYQGNHGQQTEQMLAAPEPNYVSPAEIGIPSEYNQPQAKPERKFAPKKDVQLYVPETVETPPLEIEELPEVEELRPAESPLFSAPKRDSEDSLPIPKLPSQQRNEPQSPSDIPREVQPPKAKTPQVPAFQPRTSTEPPAAATPPQQTAPTPQPPAKKAPFPGNEDDLLVPPDTHLLDSARMQRQTTGQPTYRSANRSRAVIFEPVR
>NZ_CP036292.1|WP_145120185.1|2846203_2846467_+|DNA-directed-RNA-polymerase-subunit-omega
MLEELKEEEIVNKVGGRFKLSTLIQKRLVQLNQGSRALVNVGTHDRMQIVLQEIVQDKIYLNTSNEVQTVDDMNIIPEGPDLDVSDL
>NZ_CP036292.1|WP_145120183.1|2845616_2846219_+|guanylate-kinase
MKTNTEGRLVIISGPSGAGKSTVVQSLIRECPLPLVLSVSATTRPPRPNERDGREYYFLSNQQFEDLRKDGQFLECEEVFGRGHWYGTLRPQVTTGLKQGQWVILEIDVHGAMRVLEDKELQPITIFLHPGGIEELENRLRARGTETEEAITRRLEVSVGELALMHRYRHEVINDTVDRATSEICEILKSYQERNACSKS
>NZ_CP036292.1|WP_145120203.1|2859986_2860265_+|hypothetical-protein
MSNAQRLDEVRAFLQAWFSKSHPSNVWSATESILISDGHYCGRRFAFGPYTAIWFVEENQVKIFDPDGSVAVRQDCSELFGEEPTLEIRRAA
>NZ_CP036292.1|WP_145120205.1|2860375_2861539_-|helix-turn-helix-domain-containing-protein
MRYAFRLAELLGHNPDRRRRPGTIKAIVEHTGLDRHQVASLLKNEAKYIPIEALSKLCDYLIDHGHATPAELPGALFAVRAEHFWELLARRRQLELCVGIRQGDVNDAPEQAWVVASDSVLMGALLNGVSTLGGSARHHAAGSSVNGSTKAEENPPQPERLLQTLVWSPGHVSTEETHLRANSVYESFSGAPGDKAMVCIGSVKSNPVAEVLFSEAFGCDPFVSQDDVEKASDRACPFFMRYRDFDPKPPSSTAGERLSKTEAADKPGLWVETDNGTWEWAGGGQNSDVALVFYIFREALGRLDMVLSGFTGRATRYLAKTLATRSEAFWPPVYEEPHVQIGAYIVEYETDGSKAKSEDLLMTNVSSAAKITPLSAKAIERRIVSNG
>NZ_CP036292.1|WP_145120207.1|2861798_2862821_-|molybdopterin-biosynthesis-protein-MoeB
MTRSTRYARQIQFAPIAASGQARIAAARVLVLGVGALGTVAAELLARAGVGFLRLVDRDTVEWSNLQRQSLFEESDAELQVAKAAAAAARLTRINSEIEIEAEACDVDPGNILRLMSDIDLVIDATDNFPTRLLLNDAAVKLGKPWVHGGCVGAQGQVGFFRGVDRPCFRCVVPELPEAGSVATCDTAGVLNAATHTIASLQVGQAIQWIVSGNASLQGKLQSIDLWTSRTLQIEIGKSAQANCPLCQQRSFDFLNGDFAAQPIVLCGRNAVQIPGGRAVSIDRIADQWRETGEVHQNRFLVRLNVDPFEITLFADGRAIIAGTEEVAKARSLYAQYVGQ
>NZ_CP036292.1|WP_145124101.1|2862966_2863941_+|glycosyltransferase
MDLSIIIPIFNEADSVRPLYDRLAEVMPQLPAATEIVFVDDGSTDGSSQRLDQIATRDGRVTVVHFRRNYGQTAAMQAGLEQARGRVLVTLDGDLQNDPHDIPAMLDAIDQGADLVHGWRKDRHDTWLTRKLPSLIANRLISRVTGLPIHDLGCTLKAIRAEVADELDLYGEMHRFIPVLAYARGARCHEMVVAHHARQFGTSKYGLSRTTRVVLDLITVKFLIDYMDRPMKLLGRLALAALAVSGFAGLGVAAMKLFSGIDMTGNPLLLLTVFMGIVSLQFFGLGLLGEMNTRLYYQRSSRRPFAIRSITQSASQTVAMNRAA
>NZ_CP036292.1|WP_145120209.1|2863946_2864906_-|putative-2-dehydropantoate-2-reductase
MSSKRSYAIIGTGALGGYYGGLLARAGLDVHFLLRSDFDHVQQHGLQVDSKNGNFHLPQVNAYRSAAEMPACDVTIVAIKTTANQQLAEILAATTREGGVVLVLQNGLHVEADSAAVVGPDRVLGGCCFLCSNKVGPGHIDHIDYGRIAFGEYRADGSVRPISERTREIEADLKLASIPAEAVDDLIKVRWQKLMWNIPFNGLSVVLDASTAEIMNHPASEALAEQIIRDVRAAAMQCGKSIGEAFVDKMMNDTRAMVPYDSSMRVDFKQGRPIEVEAIVGNPLRELQRHGGQSPRLEMLYQQLTFFDRRRTEEHTSRG
>NZ_CP036292.1|WP_145120211.1|2865016_2866255_-|acetylxylan-esterase
MLPTAMLSAQPAGFNYDETKVPAYTLPDPLVMADGTPVTSAEQWPKRREEIMQLFLEEVYGKAPGKPEGLHFEVFEQSDDAVNGKATRKQVRVYFDADETVAMDILIYLPKKSVEAKKPVPTYLSLNFYGNHTISNDPAVLLSESWMRSNKEQGVVDHRATEASRGALASRWPVEMIIDRGYGLATVYYGDIDPDFDDGFKNGVHALYDPPAKDGWGSIATWAWGLSRAMDYLETDPEIDTKRVAVFGHSRLGKASLWAGASDPRFSITISNDSGCGGAALSRRAFGETVAQINKTCPHWFCDNNSQYGNNESACPVDQHQLVALIAPRSAYIASAKEDTWADPRGEFLSVVHAAPVFRLLGTDGIGGKTEMPLVNKPIMHTLGYHIRTGKHDVTDFDWNAYMDFADRRWGK
>NZ_CP036292.1|WP_145120213.1|2866767_2868132_-|IS4-family-transposase
MSSDARTQNLSAAFELLKQWTDIGDADVFEELGPAAVYKTSVVLWLMLFQRLNPKASLRDAVLHFVATAPPELKTNKRLREGSLSTKSSSYSDARHRLSLKAAHWFQERVASSIVNSTAPTWGDRRVFLIDGTTFTLAPVAELQAAYPPAPNQYGESVWPIAYVVFAHELSSGAAVPEEIGAMYGPNAVSETRLAQTLMKRLPAKSIIMADAGFGIFSTAYHAHLNGHNFVLRLKKDRFNRIRKRAELIHSTATSKSYRVSWTPSAKERVTNPDLPSDCVIAAMIHELKIGEESLYLVEDIDATPKQLRDLYWKRNDIEVDIRNIKLVIGTEEIRAKSKEMFLKEFALSMVAYNLATQLRRQAAVIAECEPRELSFTGVWSVYRHMLQGIEVSAPGRWIERLGRVLHYASKQKLPNRPGRSYPREAYARRPKTTHFQKRRKKSKPNDPEDPTSK
>NZ_CP036292.1|WP_145124102.1|2868508_2869732_-|acetylxylan-esterase
MLSAQPAGFNYDEAKVPAYTLPDPLVMADGTPVTSADQWPKRREEIMQLFLEEVYGKAPGKPEGLHFKVVEQSDDAVNGKATRKQVRVFFDADETVAMDILIYLPKKSVEANKPVPTFLTLNFFGNHSISNDPAILLSESWIRSSKEKGVVKNRATEASRGASANRWPVEMIIDRGYGLATIYYGDIDPDFDDGFKNGVHALYDPPAKDGWGSLATWAWGLSRAMDYFETDDEIDAKRVAVFGHSRLGKTSLWAGASDPRFSITISNDSGCGGAALSRRAFGETVARINKSFPHWFCDNYLKYSDNEGACPVDQHQLVALIAPRSVYIASAEDDTWADPRGEFLSAVHAAPVYRLLGTDGIGGATEMPPVNKPIMHTLGYHIRTGKHDVTDFDWNAYMDFADRRWGK
>NZ_CP036292.1|WP_145120215.1|2870002_2870359_-|hypothetical-protein
MSRLRCEGWWEQQGLGRQPMEDLQIAFRDGQVSGGGRDIVGVFTLSGQLQGERALLVKQYLGSHHVDYPGSFDGEGTLQGLWSIDGFGGKWMIHVARDAANKQNREVAVIQDWPPTQA
>NZ_CP036292.1|WP_145120217.1|2870566_2871463_+|ThuA-domain-containing-protein
MALICPAPNWPLSNLLETRSMVRLLICFSLVASTAMFAIAEPARLLMVSQSVGYRHSSVNREKMPLSPAERAITELGISSGLFRVDCTQDVATDFTKEKLQHYDLVLFYTTGDLPIAQEDLDYFFNDWLKQKGHCFIGTHSAADTFHNYKPYWDMIGGTFNGHPWGAGSTVTISVHDQDHPASKPWGEEVTLKDEIYRFKNWQPEKVRVLMSLNMAKTELKEPYHVPVLWVKEYGDGKVMHMSLGHREDVWTNETYLASLLGGMKWMLGQEPGDATPNPELSAAQELKAKADTEAAKK

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Crispr_ID: NZ_CP036292_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_13

2999471-2999537

Orphan

Consensus_repeat	Method
GACGAGGCAACGAGTCCCCTCAACA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_13

>merge|NZ_CP036292|13|2999471-2999537|CRISPRCasFinder
GACGAGGCCACGAGTCCCCTCAACACAAAACGATTCGTAGTGGACGAGGTCACGAGTCCTCCCTCAC

>NZ_CP036292|13|13|2999471-2999537|CRISPRCasFinder
GACGAGGCCACGAGTCCCCTCAACA	CAAAACGATTCGTAGTG
GACGAGGTCACGAGTCCTCCCTCAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145124109.1\|2994674_2995556_-\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|223881
NZ_CP036292.1\|WP_145124110.1\|3005133_3005835_-\|DUF1080-domain-containing-protein	unknown	unknown	gnl\|CDD\|368908
NZ_CP036292.1\|WP_145120368.1\|2998379_2999378_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120385.1\|3013734_3017346_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120377.1\|3008413_3009271_-\|alpha/beta-hydrolase-fold-domain-containing-protein	unknown	unknown	gnl\|CDD\|223730
NZ_CP036292.1\|WP_145120371.1\|2999646_3003348_-\|HIT-domain-containing-protein	unknown	unknown	gnl\|CDD\|223989
NZ_CP036292.1\|WP_145120352.1\|2985452_2986364_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP036292.1\|WP_145120381.1\|3011313_3012144_-\|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP036292.1\|WP_145120375.1\|3007546_3008233_-\|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl\|CDD\|225039
NZ_CP036292.1\|WP_145120379.1\|3009338_3011288_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP036292.1\|WP_145120359.1\|2987702_2989079_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|238872
NZ_CP036292.1\|WP_145120363.1\|2990253_2991864_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238362
NZ_CP036292.1\|WP_145120373.1\|3004090_3004879_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|212491
NZ_CP036292.1\|WP_145120367.1\|2995659_2997540_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|188247
NZ_CP036292.1\|WP_145120387.1\|3017303_3017843_+\|divalent-cation-tolerance-protein-CutA	unknown	unknown	gnl\|CDD\|376987
NZ_CP036292.1\|WP_145120383.1\|3012168_3013458_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145120355.1\|2986376_2986910_+\|PH-domain-containing-protein	unknown	unknown	gnl\|CDD\|367615
NZ_CP036292.1\|WP_145120357.1\|2986906_2987626_+\|PH-domain-containing-protein	unknown	unknown	gnl\|CDD\|367615
NZ_CP036292.1\|WP_145120365.1\|2994264_2994675_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP036292.1\|WP_145120361.1\|2989124_2989982_-\|branched-chain-amino-acid-transaminase	unknown	unknown	gnl\|CDD\|236238

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145124109.1\|2994674_2995556_-\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|223881	COG0811, TolQ, Biopolymer transport proteins [Intracellular trafficking and secretion].	2.19812e-27
NZ_CP036292.1\|WP_145124110.1\|3005133_3005835_-\|DUF1080-domain-containing-protein	gnl\|CDD\|368908	pfam06439, DUF1080, Domain of Unknown Function (DUF1080). This family has structural similarity to an endo-1,3-1,4-beta glucanase belonging to glycoside hydrolase family 16. However, the structure surrounding the active site differs from that of the endo-1,3-1,4-beta glucanase.	5.28016e-39
NZ_CP036292.1\|WP_145120377.1\|3008413_3009271_-\|alpha/beta-hydrolase-fold-domain-containing-protein	gnl\|CDD\|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	7.43165e-21
NZ_CP036292.1\|WP_145120371.1\|2999646_3003348_-\|HIT-domain-containing-protein	gnl\|CDD\|223989	COG1061, SSL2, DNA or RNA helicases of superfamily II [Transcription / DNA replication, recombination, and repair].	3.72113e-69
NZ_CP036292.1\|WP_145120352.1\|2985452_2986364_+\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	1.32826e-17
NZ_CP036292.1\|WP_145120381.1\|3011313_3012144_-\|SpoIIE-family-protein-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	1.70519e-30
NZ_CP036292.1\|WP_145120375.1\|3007546_3008233_-\|carboxymuconolactone-decarboxylase-family-protein	gnl\|CDD\|225039	COG2128, COG2128, Uncharacterized conserved protein [Function unknown].	2.25007e-19
NZ_CP036292.1\|WP_145120379.1\|3009338_3011288_-\|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.	5.34755e-05
NZ_CP036292.1\|WP_145120359.1\|2987702_2989079_-\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|238872	cd01834, SGNH_hydrolase_like_2, SGNH_hydrolase subfamily. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	4.18588e-45
NZ_CP036292.1\|WP_145120363.1\|2990253_2991864_-\|hypothetical-protein	gnl\|CDD\|238362	cd00688, ISOPREN_C2_like, This group contains class II terpene cyclases, protein prenyltransferases beta subunit, two broadly specific proteinase inhibitors alpha2-macroglobulin (alpha (2)-M) and pregnancy zone protein (PZP) and, the C3 C4 and C5 components of vertebrate complement. Class II terpene cyclases include squalene cyclase (SQCY) and 2,3-oxidosqualene cyclase (OSQCY), these integral membrane proteins catalyze a cationic cyclization cascade converting linear triterpenes to fused ring compounds. The protein prenyltransferases include protein farnesyltransferase (FTase) and geranylgeranyltransferase types I and II (GGTase-I and GGTase-II) which catalyze the carboxyl-terminal lipidation of Ras, Rab, and several other cellular signal transduction proteins, facilitating membrane associations and specific protein-protein interactions. Alpha (2)-M is a major carrier protein in serum and involved in the immobilization and entrapment of proteases. PZP is a pregnancy associated protein. Alpha (2)-M and PZP are known to bind to and, may modulate, the activity of placental protein-14 in T-cell growth and cytokine production thereby protecting the allogeneic fetus from attack by the maternal immune system.	1.06729e-07
NZ_CP036292.1\|WP_145120373.1\|3004090_3004879_-\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|212491	cd05233, SDR_c, classical (c) SDRs. 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 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 prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) 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. Extended SDRs have additional elements in the C-terminal region, 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. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	2.16306e-66
NZ_CP036292.1\|WP_145120367.1\|2995659_2997540_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|188247	TIGR02795, Uncharacterized_protein_in_oprL_3'region, tol-pal system protein YbgF. Members of this protein family are the product of one of seven genes regularly clustered in operons to encode the proteins of the tol-pal system, which is critical for maintaining the integrity of the bacterial outer membrane. The gene for this periplasmic protein has been designated orf2 and ybgF. All members of the seed alignment were from unique tol-pal gene regions from completed bacterial genomes. The architecture of this protein is a signal sequence, a low-complexity region usually rich in Asn and Gln, a well-conserved region with tandem repeats that resemble the tetratricopeptide (TPR) repeat, involved in protein-protein interaction.	5.27808e-10
NZ_CP036292.1\|WP_145120387.1\|3017303_3017843_+\|divalent-cation-tolerance-protein-CutA	gnl\|CDD\|376987	pfam03091, CutA1, CutA1 divalent ion tolerance protein. Several gene loci with a possible involvement in cellular tolerance to copper have been identified. One such locus in eubacteria and archaebacteria, cutA, is thought to be involved in cellular tolerance to a wide variety of divalent cations other than copper. The cutA locus consists of two operons, of one and two genes. The CutA1 protein is a cytoplasmic protein, encoded by the single-gene operon and has been linked to divalent cation tolerance. It has no recognized structural motifs. This family also contains putative proteins from eukaryotes (human and Drosophila).	7.11991e-44
NZ_CP036292.1\|WP_145120383.1\|3012168_3013458_-\|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.	3.64671e-68
NZ_CP036292.1\|WP_145120355.1\|2986376_2986910_+\|PH-domain-containing-protein	gnl\|CDD\|367615	pfam03703, bPH_2, Bacterial PH domain. Domain found in uncharacterized family of membrane proteins. 1-3 copies found in each protein, with each copy flanked by transmembrane helices. Members of this family have a PH domain like structure.	3.89542e-11
NZ_CP036292.1\|WP_145120357.1\|2986906_2987626_+\|PH-domain-containing-protein	gnl\|CDD\|367615	pfam03703, bPH_2, Bacterial PH domain. Domain found in uncharacterized family of membrane proteins. 1-3 copies found in each protein, with each copy flanked by transmembrane helices. Members of this family have a PH domain like structure.	6.64433e-14
NZ_CP036292.1\|WP_145120365.1\|2994264_2994675_-\|biopolymer-transporter-ExbD	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	5.75997e-26
NZ_CP036292.1\|WP_145120361.1\|2989124_2989982_-\|branched-chain-amino-acid-transaminase	gnl\|CDD\|236238	PRK08320, PRK08320, branched-chain amino acid aminotransferase; Reviewed.	0

>NZ_CP036292.1|WP_145120368.1|2998379_2999378_+|hypothetical-protein
MSWFQQLTGIDESSPQQVRAQLSVDGEDLVCPDGTRIACGRLETPTLVELRARAAATDSPRGRLSLREIVADVRRLHADPGNANSLFQVASQFNLLEMASPTVTPERGVGIYEHDHTQGPACAVACGAGTIYRNYFAAVGDCVGQSRDHQIDCSADLGRLLGNREQQLWRMQNGYLFPTDSGLRQISRTLESAAAGELDSYRDALRIGLQWNTAVTLAGSSHRVSQAYCSALPVAYGSQPAADWTAFAKLVLEAAYEATLAAAVVNLAETGSNKLYLTLLGGGVFGNRNEWIIAAIERAVASYRETPLDIAIVSYGASHPAVAALVQQFSKS
>NZ_CP036292.1|WP_145120367.1|2995659_2997540_-|tetratricopeptide-repeat-protein
MRKQAFFLNLRTIFTAFLITLGVSATAEDSFRAGLAELAAGSFEKAAATLAEFVKKNPEHPAAVQAMCGNGQALSAMGRNAEAADVFEAALKRRSNRVREAPIRLSCAKCQLHAGRYSAAAEHAHQAIQVSTSPSERAAAYPMLISALCEDERCSEAWLHLQKGADSGELDPNVTVSLAKKVAADALKQGEAKTAREAFGWQMENDQDDRGKQEAALGYAWAQAALATTPTEAADALLEYVDNYPKSPGAARALLAAARKQIDADQTPVAIELLQRLYAQYADASETVDGLTLLIQIAQKAGDEELLQETRAHLAQQHTDTPAARSVLHLAIADAAKSGDDAKFEAVASVVFNAGDPQLVAQTLDRLSETAGNEIVLRFADAGLQRMIDPQQHIVTGAIIDWLFEHQHWSVITEATAKMPAEVLVSNQHQGAVIAESLQRLGSSKAAYDLFTRLAAGSEPTFVVLLRRSELAVQVGSVDEATQAIAAATAAAESSRDRQYVQIVAAQLAIRRADFDSSRKLLDTVVLSPAADQRLRGRAQWLIGETYFMQRDYRAAIDAYRRCETLFPESGWGAAALLQAGKAFEKMGNFRDAAVCYTSLLNKHAKSPYARLASRRLGWIGNETTR
>NZ_CP036292.1|WP_145124109.1|2994674_2995556_-|MotA/TolQ/ExbB-proton-channel-family-protein
MLAFAISVPGIAAAQQFRQPGQSFQQQGFGQQGGFAPQPTAIPSIPPAAQPQPTAEAPAEETGEESSSWVPGWASSLKSQISAGGLLMIPLGICSLIVIGLICERLISLRRGRVIPRPFVRRFREKLDDGQLDIEEANEVCNEFDCAVADVFIAAVKRTGRPMVEIEAAVFDALERTADGLRRYLRVFHAVSNVAPLIGLLGTVLGMIDAFETMASEAGAGHPELLAVGISQALVTTAGGLSVAIPAYLAYMYFSSRADGYLAEIERLSLGVIDAVSAESGGAAPKARRRKAA
>NZ_CP036292.1|WP_145120365.1|2994264_2994675_-|biopolymer-transporter-ExbD
MAYQRRSGEEATINLTPMIDVVFLLVIFFMVGAKFTDQEGSIKVNVPGVGNLQSITRGPDQRVVDVLADGSLLLDKNPVAINQLQQTLTSAAAQYADTSVVVRGDGQGNFQAIAEVLQVVRQAGITDMGIAVRMQR
>NZ_CP036292.1|WP_145120363.1|2990253_2991864_-|hypothetical-protein
MTAPPTPPHPDPTPPPAAGLDAARQTTPTAPPAITPPPSALLQLDSLADEQENQQPLPATQAFLRDARVPAWLVSGLLHGGVLLFLALWTVVGTTSNLFTIQARFEREAPMPIELTPPMDRPIVEIRQTEAMPDHAIEAAVEAVEFEKPEALTATAPTKPLDTIRKMIDGLQQPTSTPALRMRGNAGIEGRVAGKRQELAEKYGASDASEQAVEAALDWLVAHQQNNGSWDFDLSHAPCNGQCRNPRSNPDGQATPKTAATGLALLPFLGAGYTHRSGKHAETVSRGLYYLRSQLRDAAVGRELMHGSMYGHGIATLAVAEAYAMTKDEDLVGMLRDLQSFIVMAQHEKGGWRYNPGQPGDMTITGWQIMALKSCQIGGLPFPTSVHSRAEDFVTSLGSQQGSRFGYLEPVAEATPTAVGLLLQMYLSKPPGDAAIMEGCHYLYELGPSKTNVYFNYYATMTLHHARYYGFPEWNAKLRDYLVKTQSRRGHEVGSWHFTDRFGNVGGRLYSTAMCALVLETYYRYLPLWAEAEFPL
>NZ_CP036292.1|WP_145120361.1|2989124_2989982_-|branched-chain-amino-acid-transaminase
MSLQISLNGQLVPKEDAKISVFDHGLLYGDGVFEGMRSYAGKIFKLDDHLDRLWDSARAICLELPITREQLAEDCKATLAANNIIDGYIRLIVTRGAGSLGLDPNRCTNPQVIIIADKISLYPSEYYENGLHLVTASTIRNHPAALSPRVKSLNYLNNIIAKMEGLQAGCVEALMLNHKGDVAECTGDNVFIVDRGVLKTPSTDSGILEGITRNAVLEIAADLGIPTREMTLTRHDLFVADECFLTGSAAEVVPVVQLDNRPIGDGKPGPITKRLLEAFHKLVRQ
>NZ_CP036292.1|WP_145120359.1|2987702_2989079_-|SGNH/GDSL-hydrolase-family-protein
MVSMFRSLALCSLLSPLFAFTALGQPATSPAAPPKLGPYLYETKPDDPAFASFNPRRAPQPGELLLRKGDRLAICGDSITEQKMYSRLIETYLTVCVPELEITARQYGWSGEKTDGFLRRMEKDCLTFSPTIATLAYGMNDSRYRPFDVTNGQWYEDHYTAIVQKFKANDVRVVVGSPGCAGKIATWVKSRSGTLEQHNLNLCALRDIAIGVAEREQVRFADIFWPMLQAQVFAPAQHGATEEKPYRVAGSDGIHPGWAGQVIMAWTILRSLGLDGDLGTIEIDTDKNTATANGGHSIDSYADGVATVTSTRYPFCATGTLHSENSIRSGMTLVPFNEDLNRFLLKVNAADGTKWEITWGDQTQTYNADQLAQGINLAWEFPKNPFSESFDRVDAAVAKKQAYETLQVKKIFHGPEGKKDFDAAVKETEAVRKPLADAIADAMQPVTHKIAIRQVAGE
>NZ_CP036292.1|WP_145120357.1|2986906_2987626_+|PH-domain-containing-protein
MTAPAPRSAQWLYRGVWKILVDCFRVPDHPPTLPVVDGGFYRSFQPSRRFLSYLKFNFWVIAAVIDLVIAVALAAVAIEEEKLAMLLAVLAIPLILAGHLVVYIALHLRYDTMWYVITDRSLRARRGIWVIYEHTITFENVQNVYLRRGPLQHLFGISELVVETAGSSQGEAESPFASGNKLLVQGIEDAAELREQIMSRVSQSRSAGLGDDQTTSPTSGFSPRHVAMLCEIRDEIKGL
>NZ_CP036292.1|WP_145120355.1|2986376_2986910_+|PH-domain-containing-protein
MTESPPPTQPSDAMFDASKITRPDDSLLVYYALVAACTVIGFPFVFIPLWIRFKTLSYRFDDTGVSMCWGYFFRREVHLTYRRLQDIHVTRNIVERWMGLSKLPLQTASGTAGATMQIEGIRDPEPLRDFLYAQMRGARNDSLDPESVDSDDQVLGVLTEIRDELRRIRNVPEGDDR
>NZ_CP036292.1|WP_145120352.1|2985452_2986364_+|TIM-barrel-protein
MQVSRRQFSATCAAAGAALALPQFARAANSGFQFRYLLGSCMYGYAPVAEILPEVAKTGSVALDIWPKAHGDQREQLDAMGEEAFATLLKQHNVQLGCITQYKLGPFGLQDEMRLAQRLGCSTIVTGGKGPKGLQGGELKRGVAKFVEQMKPHLAVAEETGVTIAIENHGNNLIESPDSLRWLIDLCPSDHLGIALAPYHLDQDSNLLAELILALGDRLSVFYAWQYGMGCMKKLPKRQELLQMPGRGELDFAPLVDALVETKFSGWTEIFMHPVPRGIPILESTDKVTTEINRSRAYLEDLI
>NZ_CP036292.1|WP_145120371.1|2999646_3003348_-|HIT-domain-containing-protein
MTSPFLQVAQADWIAANALAFAIFDGYPVATGHALVVTRRLVPTWFDATPAEQVALMELVNVVKEKLDETLRPRPDGYNVGFNSGAASGQTVDHVHIHVIPRYLGDVEDPRGGVRHVIPDKANYLAPPADSQAHDQENSGPTLSIGYPESPLWDQLAWRIVAAKSVDVLVSFVQSSGLEVIEERLFEAIANQAVVRILVSDYLYISDPRALRTLLGWCDLATESVPAGQLQAKLIETAKLSSRPASFHPKAWRIVEGASDFISVGSSNLSKPALLTGVEWNLLSSTKEPATSHTQFSEAFDSLWDVASPLTPASVTEYTAAAKTYHQTHVVPNQPEAQEIPNPRPWQLEALKSLAQIRAAGHRRALVAVATGMGKTWLAALDACQYGMTIKRRPRVLIVAHRAHILAQAEAVVSRMLDHRFAEGSTAWYIGDRSELAGELVVASVQKLSRPEGLQRLADEHFDYLIMDEVHHAHAPSYRRVLAQIRCDFALGLTATPERTDGVDVATIFDDNLAYHATIGDGISEDALVPFHYVGIKDTVDFRQIPWRNGRFDVAELEVQVEQSERMQKLWLAMENHPAKRTLVFCCSRRHALFARDWLRTKGVSAAAVFSGDGSDAYGESLDQLRDGKLQALCVVDMFNEGLDIPAVDRVVMLRPTESKIIFLQQLGRGLRAAEGKSRLLVLDFVGNHRIFAQRIVHLLSLQSGCDQWQSLRDWLAGKPLQLPEGCLLDVELDAKDMLKEFLPQGRTAAIEGYRGLRDELGRRPTAMEVFSRGYLPRAISAAEGSWFEFVHAEEDLDPDEAEVVSRFTDWLKTLETTNLNKSYKMVVLRVLLDSGQLFAGVDLFDFAKQCRSYMQRHDVLRRDLEGTQHAIDHDKATDQEWAKWWIKWPISRWLAPQNNAVWFKRSGDRFETTIDCPVHVRAALESMTEELVDWRLAAYTRSRRLTATESPEHIVFEAKVSHASGRPILFLPDKSKVPGRPVGPTPMQLPDGAMWEFKMVKIACNVAAPAGETKNQLGELLKSWFGPDAGLPGTNFRVLFKSQNGRWSVAPCDVEATDASEPATTESSEIPQILPEISDPKKFTTHAPVYDLSVAAGQWGPEGVPAEIGWIAVDDRRLEKGMFAAHVIGHSMEPVIPNDAWCLFRPITPGTREGKLLLVQVNTHLDPEEGGRYTVKRYHSTKRVDEDGWQHTTIQLQPLNPDYKPIDITPEDAEDLRVIGEFICVIDPAQGT
>NZ_CP036292.1|WP_145120373.1|3004090_3004879_-|SDR-family-NAD(P)-dependent-oxidoreductase
MDLGLKNKLAVITGSTSGIGQAIAKSLLDEGATVVINGRSQTSLARATKELGGGDSLHGVAADVSTADGCAALVAAAEAIAPIDILINNAGIFEPKPFAEISDEDWQRFYEVNVMSGVRMSRAVMGSMQQRGWGRIVFISSESAINIPTEMVHYGMTKTAQLSISRGLAKTLKDTGVTVNCVLPGPTWSEGVEQFVESLAGEQDIEQVKRDFFRDSRGGSLIQRFASVEEVASLVSYVVSQRASATTGAALRCDGGLVDTCF
>NZ_CP036292.1|WP_145124110.1|3005133_3005835_-|DUF1080-domain-containing-protein
MKDTNSTSISRDYTMQMNRLTRNTAVAAFSIFAALCSTVAVTAEENKSSGDEAAWISLFDGKSMEGWEKVGSDGSKWEVKEGAIWGSGTPSMLVNTTGPYKNFRYRAEVKINDGGNSGLYFRTTRRPGFSDGYEAQIDSTHTDPIRTGSLYGFCHVYPQLVKPGTWFTYEIEVRDDVWRGREMTRIKITVDGNELYEYLDFEKTYGPGHFAFQQHDPGSTVAIRQAEVQPLAD
>NZ_CP036292.1|WP_145120375.1|3007546_3008233_-|carboxymuconolactone-decarboxylase-family-protein
MPSTARWPPVLQLTARDCAHPGLPQDKPQIDRQPSPSSFTPVFQAKERSTMPRLKTIGPNEAQPPLKEIYDDLTSQMGKVVNIFQGMGNSPAALKAYLSMSAALAEGDLSPEDREIIYLAVSEQNGCHYCVSAHAMLAKRVGLADDAIRAARQFQSSDPKHESLLTFVRRVIASKGFVSDEELQAVKSAGYSDGQIAEAVGYIGLATFSNLFNHVNGTELDFPAAEKI
>NZ_CP036292.1|WP_145120377.1|3008413_3009271_-|alpha/beta-hydrolase-fold-domain-containing-protein
MKRTLAPAIRLAILFLLPLAAFPSLASAQQKEKQSQEYKIDADVPYRSGDDLPESMQRCRLDVYYPVDRKDFATVVWFHGGGLTAGNKSIPQGLKNRGIAVVAVNYRLGPAVKSPAYIEDAAAAVAWTFNHIADYGGSRDRIYVSGHSAGGYLTSMVGLDRRWLAAHDIDANEIAGLIPFSGHTITHFTIRKERGIGGKQPVVDDLAPLYHVRKDAPPLLLITGDRELEMLGRYEENAYLWRMMQVVGHPNTELLELDGYDHGGMDDPAYPLMLKFIRKDLASKR
>NZ_CP036292.1|WP_145120379.1|3009338_3011288_-|tetratricopeptide-repeat-protein
MRPKMVLSMPTPILSARTTTAGLAIAMLSVWLSCSPLAAADAPLAPPSDVELRAQVDRLIEQLGDPSYAKRIRARGELQRMGLMAFDALHAAQLNDDSEIAMAARYLVESLQVSWSTEDDSTDVRQILSEYGAQTEVERKSRMDRLAGLPQREGLAALCRLVRFETKLRLSRAAALLIMQQPTSDSIELRRRNSAVIAESLGANSREASKWLTLYARDLANDEFNVSAWRALIESERSRVASQTTRSSDDLAVLKLYRICAVRAMEHGLQAESLALATESLELVEARKQPLRNAVEWALDHQMWTIVLKLLQRDASDFKNDAWLSYAVAEALTETGDAAEGERWVSQALELAPLAPLNEDGSSPMTADARQQATQRHMLVAMELVSRGRFDWAKREYQYVIDRSPIDTSSSADSRWKLAMILSEFEDYQPAAELLEPSVQRMMMDRDFRRIVQRELIYSFEDFESRMHYNAALGHQQAGENEQAAASLKSALAAAPLDGDILIAMYRFPGDEKWKQETQRAIREALTEFERMIREGERQAAGLNQQQLNRGISHYCNQYAWLAANTNGDLKRALAYSRRSLELMPKRASLTDTLSHCYYALGDYDAAVRTQREAVALEPHSPPIRRQLDFFIEKQQEHREKQNAAVRKD
>NZ_CP036292.1|WP_145120381.1|3011313_3012144_-|SpoIIE-family-protein-phosphatase
MELNSGNPGPAVIYCNRRMTASVAHAIGGGESAVFSSRSPCKETPNEDVAAIVPCDENSCVLIVADGMGGHSAGEVASLTAVREMIRAVNEALQQKQMLRIGIINGFERANDAVQAMGTGSGTTLAVVEISQNEVRPYHAGDSVVLVVGSRGKIKLETTSHSPVGFGLAAGLLDSSEAMDHAERHVILNAVGSPSMRIEIGSAIRLAARDTVMLASDGLTDNVTTQEAIRRIRKGKICDCANELTELATQRMWNPGEGRPSKPDDLTVLLFRRQSG
>NZ_CP036292.1|WP_145120383.1|3012168_3013458_-|protein-kinase
MIKSRQKLGKYQIEKKLGEGGFAGVYRALDTIEGVRVALKIPYSQSLSSDTLEECLKEVRMMASLDHPHILSLKNAEFIEGHFVLAFPLAEQTLGDRITKRMSMAQGISYTEQMLEAVSYAHQRRIIHCDLKPENMVLFANGDLRLTDFGIAKIAMRTLRASGSGTVGYIAPEQAMGRPSFRSDVFSLGLVLYRVFSGKLPEWPFAWPPPNYRALCDRVSPEFVEMLRRSLQMEPQRRYRNATQMLSAFRRLKARAILNNEATANAGKKKKTGRDWRTLRYQQFLRNYGKVIDVNGSCKKCKGPVAESMIACPWCSSDRQMHVRETRFPQVCPRCEGGMKLDWSFCPWCEGPEFELGSTRSFTDKRYTTSCDNEECGGRLMPFMRFCPWCDTRVQRTWNLTGSKDKCRSCGWGVSREFWSCCPWCATDI
>NZ_CP036292.1|WP_145120385.1|3013734_3017346_-|hypothetical-protein
MQRIDNDMDEAIETSRRRTDQMRQRRRTRYRIAMGSFALTILLSIAMGPSIVCNSPIADSLLGSNAEKYGWQAKAYGIRLGWMTPLRLDDLELIGPSGQTRLTAGRIETEVTLIDLISGRSDFGTVQATGLRSELAVDAGTSSLEQDLAAFESEPDSTTDESDDDSSSLDTSTSVKIVLRDAEVVVTNATTGEVWKLAEIAADIAVESDLPRGDLSLTVVDPQGQPGKLELRLAASEQSGASALQVDATLASLPLSIAKLLATRFPTDDGMAPQHVGGVAEGDLRLTLDASGALRGDFRSLNLRDVQIGDPRLSENLWAIQAARVEGSFLYTATHLQGMGLHLSSDFGVADLNGTFRIASADVSADLAENPFAWLEALSGTAGLEIDLARLSKAAPGLLPLRENASIESAILRGSLSGIQDADGFLTNIDLESDPIRATSFGRPLQIEPMTIQLSARPSGAWIMAERLQIRSMFANATASGDLRNGQAEFNIDLGRLTAMVSPLIDLSDTELGGSTSGSIRWTAERDGLWRLDGQATAAMLAIGLSGGETIREPAVDFKIGAIGIWGGDHLARLNQAAITLRNASQMWDIELEQPIDQPTSKTLLPVKAVGKGRIAAVVGLIRPWLPTAMGATEGEFDATLHADVAMGDGVLRGATISMQQPAVAWSGSRYSQSTLKVNFDGKLPMAMDTISIRSLTAIGNAAALSAQGDYRYEGNSELELAWRADVERLRQSTDAIAAQFQPIQLTSFAPQPEVEASNYQIKGTIEGRATLLGSGGIWKANVDADAANLELLQNVGVSGHVDLANHVPPMPLQVNHESLWKEPNLKLVGLIQYNEANGDIDGKDLKISTQWLDATLTGKYRGDETTTQVAMSGPARIRSDEIARRLQDLIGQPIQMSGTSEGPIELQVRMQGDEPADITASGTLAWDQANIAGVEIGPASIPVKTAAGQIEIAPTTIQLAKGRLNLAGKASYSDDPIWIQPTPGLIAEGVQLETEMTRTWLKYVAPLLADATDVNGTFKLEIDQAMIFPMAPARNKISGRLGIDHAQVGPGPIANSVVGVIGQFASLGGSKPLTAGNQWIELPAQSVDFVMENGVVTHQRLMMQLDDVRVVSSGSASLDGRLEINAQIPIEDAWAGNDMRKAGMVGQTFQIPIDGTFSRPSLDSRGVTESLTRLGTKALEETAKNALQKELSRGLQKLFGNR
>NZ_CP036292.1|WP_145120387.1|3017303_3017843_+|divalent-cation-tolerance-protein-CutA
MSRLLRPCRYRCVASRASCSIGNPLRQTHPRHICPGRAFGVCAGATYHYEKPVDSKQNRSPSPTSFLELISLDGFLLITTTTPTEDEARRIASRLIELRYAACVQVEGPISSHYRWEGSVHCDPEFRLSIKTVGSRYDVVERLIAEMHSYQQPQIIATPIVAGAEGYLNWLTEQTQTEC

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Crispr_ID: NZ_CP036292_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_14

3019724-3019820

Orphan

Consensus_repeat	Method
GGTGGTTTACACCACCGGCATTAGAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_14

>merge|NZ_CP036292|14|3019724-3019820|CRISPRCasFinder
GGTGGTTTACACCACCGGCATTAGATGTGGCGCCCTCCGGGCTCAGGAGTTTAAAAGTGCGGAATCACTCTGGTGGTTTACACAACCGGCATTAGAT

>NZ_CP036292|14|14|3019724-3019820|CRISPRCasFinder
GGTGGTTTACACCACCGGCATTAGAT	GTGGCGCCCTCCGGGCTCAGGAGTTTAAAAGTGCGGAATCACTCT
GGTGGTTTACACAACCGGCATTAGAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145120404.1\|3028691_3029768_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145120400.1\|3026988_3028158_+\|TonB-dependent-receptor	unknown	unknown	gnl\|CDD\|368307
NZ_CP036292.1\|WP_145120406.1\|3032659_3033781_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274618
NZ_CP036292.1\|WP_145120377.1\|3008413_3009271_-\|alpha/beta-hydrolase-fold-domain-containing-protein	unknown	unknown	gnl\|CDD\|223730
NZ_CP036292.1\|WP_145120381.1\|3011313_3012144_-\|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl\|CDD\|223704
NZ_CP036292.1\|WP_145120398.1\|3024345_3025992_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293751
NZ_CP036292.1\|WP_145120379.1\|3009338_3011288_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP036292.1\|WP_145124110.1\|3005133_3005835_-\|DUF1080-domain-containing-protein	unknown	unknown	gnl\|CDD\|368908
NZ_CP036292.1\|WP_145120387.1\|3017303_3017843_+\|divalent-cation-tolerance-protein-CutA	unknown	unknown	gnl\|CDD\|376987
NZ_CP036292.1\|WP_145120389.1\|3017959_3019168_+\|ethanolamine-utilization-protein	unknown	unknown	gnl\|CDD\|183423
NZ_CP036292.1\|WP_145120394.1\|3020855_3021506_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120373.1\|3004090_3004879_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|212491
NZ_CP036292.1\|WP_145120385.1\|3013734_3017346_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120396.1\|3021552_3024162_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|293786
NZ_CP036292.1\|WP_145120392.1\|3020077_3020803_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120402.1\|3028216_3028471_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145120383.1\|3012168_3013458_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145120405.1\|3030359_3032663_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378650
NZ_CP036292.1\|WP_145120407.1\|3033889_3036103_-\|1,4-alpha-glucan-branching-protein-GlgB	unknown	unknown	gnl\|CDD\|235445
NZ_CP036292.1\|WP_145120375.1\|3007546_3008233_-\|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl\|CDD\|225039

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145120400.1\|3026988_3028158_+\|TonB-dependent-receptor	gnl\|CDD\|368307	pfam05150, Legionella_OMP, Legionella pneumophila major outer membrane protein precursor. This family consists of major outer membrane protein precursors from Legionella pneumophila.	2.21109e-08
NZ_CP036292.1\|WP_145120406.1\|3032659_3033781_-\|hypothetical-protein	gnl\|CDD\|274618	TIGR03508, decahem_SO, decaheme c-type cytochrome, DmsE family. Members of this family are small, decaheme c-type cytochromes, related DmsE of Shewanella oneidensis MR-1, which has been shown to be part of an anaerobic dimethyl sulfoxide reductase.	1.29761e-05
NZ_CP036292.1\|WP_145120377.1\|3008413_3009271_-\|alpha/beta-hydrolase-fold-domain-containing-protein	gnl\|CDD\|223730	COG0657, Aes, Esterase/lipase [Lipid metabolism].	7.43165e-21
NZ_CP036292.1\|WP_145120381.1\|3011313_3012144_-\|SpoIIE-family-protein-phosphatase	gnl\|CDD\|223704	COG0631, PTC1, Serine/threonine protein phosphatase [Signal transduction mechanisms].	1.70519e-30
NZ_CP036292.1\|WP_145120398.1\|3024345_3025992_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293751	cd16027, SGSH, N-sulfoglucosamine sulfohydrolase (SGSH; sulfamidase). N-sulfoglucosamine sulfohydrolase (SGSH) belongs to the sulfatase family and catalyses the cleavage of N-linked sulfate groups from the GAGs heparin sulfate and heparin. The active site is characterized by the amino-acid sequence motif C(X)PSR that is highly conserved among most sulfatases. The cysteine residue is post-translationally converted to a formylglycine (FGly) residue, which is crucial for the catalytic process. Loss of function of SGSH results a disease called mucopolysaccharidosis type IIIA (Sanfilippo A syndrome), a fatal childhood-onset neurodegenerative disease with mild facial, visceral and skeletal abnormalities.	5.49118e-153
NZ_CP036292.1\|WP_145120379.1\|3009338_3011288_-\|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.	5.34755e-05
NZ_CP036292.1\|WP_145124110.1\|3005133_3005835_-\|DUF1080-domain-containing-protein	gnl\|CDD\|368908	pfam06439, DUF1080, Domain of Unknown Function (DUF1080). This family has structural similarity to an endo-1,3-1,4-beta glucanase belonging to glycoside hydrolase family 16. However, the structure surrounding the active site differs from that of the endo-1,3-1,4-beta glucanase.	5.28016e-39
NZ_CP036292.1\|WP_145120387.1\|3017303_3017843_+\|divalent-cation-tolerance-protein-CutA	gnl\|CDD\|376987	pfam03091, CutA1, CutA1 divalent ion tolerance protein. Several gene loci with a possible involvement in cellular tolerance to copper have been identified. One such locus in eubacteria and archaebacteria, cutA, is thought to be involved in cellular tolerance to a wide variety of divalent cations other than copper. The cutA locus consists of two operons, of one and two genes. The CutA1 protein is a cytoplasmic protein, encoded by the single-gene operon and has been linked to divalent cation tolerance. It has no recognized structural motifs. This family also contains putative proteins from eukaryotes (human and Drosophila).	7.11991e-44
NZ_CP036292.1\|WP_145120373.1\|3004090_3004879_-\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|212491	cd05233, SDR_c, classical (c) SDRs. 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 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 prostaglandin dehydrogenase (PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, PGDH numbering) and/or an Asn (Asn-107, PGDH numbering) 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. Extended SDRs have additional elements in the C-terminal region, 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. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	2.16306e-66
NZ_CP036292.1\|WP_145120389.1\|3017959_3019168_+\|ethanolamine-utilization-protein	gnl\|CDD\|183423	PRK12306, uvrC, excinuclease ABC subunit C; Reviewed.	1.76816e-32
NZ_CP036292.1\|WP_145120396.1\|3021552_3024162_+\|hypothetical-protein	gnl\|CDD\|293786	sd00045, ANK, ankyrin repeats. Ankyrin repeats are one of the most abundant repeat motifs, and generally function as scaffolds for protein-protein interactions in processes including cell cycle, transcriptional regulation, signal transduction, vesicular trafficking, and inflammatory response. Although predominantly found in eukaryotic proteins, they are also found in some bacterial and viral proteins. Less is known of their physiological roles in prokaryotes. Some bacterial ANK proteins play key roles in microbial pathogenesis by mimicking or manipulating host function(s). The pathogen Providencia alcalifaciens N-formyltransferase ankyrin repeats function in small molecule binding and allosteric control. Ankyrin-repeat proteins have been associated with a number of human diseases.	6.21445e-13
NZ_CP036292.1\|WP_145120404.1\|3028691_3029768_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	6.71816e-54
NZ_CP036292.1\|WP_145120383.1\|3012168_3013458_-\|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.	3.64671e-68
NZ_CP036292.1\|WP_145120405.1\|3030359_3032663_-\|hypothetical-protein	gnl\|CDD\|378650	pfam11377, DUF3180, Protein of unknown function (DUF3180). Some members in this family of proteins are annotated as membrane proteins however this cannot be confirmed. Currently there is no known function.	0.000278072
NZ_CP036292.1\|WP_145120407.1\|3033889_3036103_-\|1,4-alpha-glucan-branching-protein-GlgB	gnl\|CDD\|235445	PRK05402, PRK05402, 1,4-alpha-glucan branching protein GlgB.	0
NZ_CP036292.1\|WP_145120375.1\|3007546_3008233_-\|carboxymuconolactone-decarboxylase-family-protein	gnl\|CDD\|225039	COG2128, COG2128, Uncharacterized conserved protein [Function unknown].	2.25007e-19

>NZ_CP036292.1|WP_145120389.1|3017959_3019168_+|ethanolamine-utilization-protein
MDLHQPTGLFEGFGPNPLDPLGPRTTHRVAATSTAELRTLVRQQCPKSPGIYGMLDRSGQLIYVGKSKRLRIRLLSYFSPRNAEEKAGRIIQAAQTVLWETQPSEFAALLREQQLIRRWTPRWNVQEIPKRQRPVYLCLGGAPAPYFFLDAMPPADVVASEGPFRGAGKMQRAVDALNNFYRLRDCSSKQELYFADQLQLFELEQRPGCLRYEIGRCSGPCVGQCTRRQYYQQVAEAESFLDGFHAAPLETIRETIHRAAEMRQYELAGRMSRDLVSLEYLHRKLMFLAAARRKYTFVYSVPGHESEPDAQQNHRGVWYLIRRGEVCESIVAPRCPEEFQRARRRVTHWKRVLADPENHRAASPFPFTLSLVAQWLRKQPQELERTFHPSEAGRRYRALARS
>NZ_CP036292.1|WP_145120387.1|3017303_3017843_+|divalent-cation-tolerance-protein-CutA
MSRLLRPCRYRCVASRASCSIGNPLRQTHPRHICPGRAFGVCAGATYHYEKPVDSKQNRSPSPTSFLELISLDGFLLITTTTPTEDEARRIASRLIELRYAACVQVEGPISSHYRWEGSVHCDPEFRLSIKTVGSRYDVVERLIAEMHSYQQPQIIATPIVAGAEGYLNWLTEQTQTEC
>NZ_CP036292.1|WP_145120385.1|3013734_3017346_-|hypothetical-protein
MQRIDNDMDEAIETSRRRTDQMRQRRRTRYRIAMGSFALTILLSIAMGPSIVCNSPIADSLLGSNAEKYGWQAKAYGIRLGWMTPLRLDDLELIGPSGQTRLTAGRIETEVTLIDLISGRSDFGTVQATGLRSELAVDAGTSSLEQDLAAFESEPDSTTDESDDDSSSLDTSTSVKIVLRDAEVVVTNATTGEVWKLAEIAADIAVESDLPRGDLSLTVVDPQGQPGKLELRLAASEQSGASALQVDATLASLPLSIAKLLATRFPTDDGMAPQHVGGVAEGDLRLTLDASGALRGDFRSLNLRDVQIGDPRLSENLWAIQAARVEGSFLYTATHLQGMGLHLSSDFGVADLNGTFRIASADVSADLAENPFAWLEALSGTAGLEIDLARLSKAAPGLLPLRENASIESAILRGSLSGIQDADGFLTNIDLESDPIRATSFGRPLQIEPMTIQLSARPSGAWIMAERLQIRSMFANATASGDLRNGQAEFNIDLGRLTAMVSPLIDLSDTELGGSTSGSIRWTAERDGLWRLDGQATAAMLAIGLSGGETIREPAVDFKIGAIGIWGGDHLARLNQAAITLRNASQMWDIELEQPIDQPTSKTLLPVKAVGKGRIAAVVGLIRPWLPTAMGATEGEFDATLHADVAMGDGVLRGATISMQQPAVAWSGSRYSQSTLKVNFDGKLPMAMDTISIRSLTAIGNAAALSAQGDYRYEGNSELELAWRADVERLRQSTDAIAAQFQPIQLTSFAPQPEVEASNYQIKGTIEGRATLLGSGGIWKANVDADAANLELLQNVGVSGHVDLANHVPPMPLQVNHESLWKEPNLKLVGLIQYNEANGDIDGKDLKISTQWLDATLTGKYRGDETTTQVAMSGPARIRSDEIARRLQDLIGQPIQMSGTSEGPIELQVRMQGDEPADITASGTLAWDQANIAGVEIGPASIPVKTAAGQIEIAPTTIQLAKGRLNLAGKASYSDDPIWIQPTPGLIAEGVQLETEMTRTWLKYVAPLLADATDVNGTFKLEIDQAMIFPMAPARNKISGRLGIDHAQVGPGPIANSVVGVIGQFASLGGSKPLTAGNQWIELPAQSVDFVMENGVVTHQRLMMQLDDVRVVSSGSASLDGRLEINAQIPIEDAWAGNDMRKAGMVGQTFQIPIDGTFSRPSLDSRGVTESLTRLGTKALEETAKNALQKELSRGLQKLFGNR
>NZ_CP036292.1|WP_145120383.1|3012168_3013458_-|protein-kinase
MIKSRQKLGKYQIEKKLGEGGFAGVYRALDTIEGVRVALKIPYSQSLSSDTLEECLKEVRMMASLDHPHILSLKNAEFIEGHFVLAFPLAEQTLGDRITKRMSMAQGISYTEQMLEAVSYAHQRRIIHCDLKPENMVLFANGDLRLTDFGIAKIAMRTLRASGSGTVGYIAPEQAMGRPSFRSDVFSLGLVLYRVFSGKLPEWPFAWPPPNYRALCDRVSPEFVEMLRRSLQMEPQRRYRNATQMLSAFRRLKARAILNNEATANAGKKKKTGRDWRTLRYQQFLRNYGKVIDVNGSCKKCKGPVAESMIACPWCSSDRQMHVRETRFPQVCPRCEGGMKLDWSFCPWCEGPEFELGSTRSFTDKRYTTSCDNEECGGRLMPFMRFCPWCDTRVQRTWNLTGSKDKCRSCGWGVSREFWSCCPWCATDI
>NZ_CP036292.1|WP_145120381.1|3011313_3012144_-|SpoIIE-family-protein-phosphatase
MELNSGNPGPAVIYCNRRMTASVAHAIGGGESAVFSSRSPCKETPNEDVAAIVPCDENSCVLIVADGMGGHSAGEVASLTAVREMIRAVNEALQQKQMLRIGIINGFERANDAVQAMGTGSGTTLAVVEISQNEVRPYHAGDSVVLVVGSRGKIKLETTSHSPVGFGLAAGLLDSSEAMDHAERHVILNAVGSPSMRIEIGSAIRLAARDTVMLASDGLTDNVTTQEAIRRIRKGKICDCANELTELATQRMWNPGEGRPSKPDDLTVLLFRRQSG
>NZ_CP036292.1|WP_145120379.1|3009338_3011288_-|tetratricopeptide-repeat-protein
MRPKMVLSMPTPILSARTTTAGLAIAMLSVWLSCSPLAAADAPLAPPSDVELRAQVDRLIEQLGDPSYAKRIRARGELQRMGLMAFDALHAAQLNDDSEIAMAARYLVESLQVSWSTEDDSTDVRQILSEYGAQTEVERKSRMDRLAGLPQREGLAALCRLVRFETKLRLSRAAALLIMQQPTSDSIELRRRNSAVIAESLGANSREASKWLTLYARDLANDEFNVSAWRALIESERSRVASQTTRSSDDLAVLKLYRICAVRAMEHGLQAESLALATESLELVEARKQPLRNAVEWALDHQMWTIVLKLLQRDASDFKNDAWLSYAVAEALTETGDAAEGERWVSQALELAPLAPLNEDGSSPMTADARQQATQRHMLVAMELVSRGRFDWAKREYQYVIDRSPIDTSSSADSRWKLAMILSEFEDYQPAAELLEPSVQRMMMDRDFRRIVQRELIYSFEDFESRMHYNAALGHQQAGENEQAAASLKSALAAAPLDGDILIAMYRFPGDEKWKQETQRAIREALTEFERMIREGERQAAGLNQQQLNRGISHYCNQYAWLAANTNGDLKRALAYSRRSLELMPKRASLTDTLSHCYYALGDYDAAVRTQREAVALEPHSPPIRRQLDFFIEKQQEHREKQNAAVRKD
>NZ_CP036292.1|WP_145120377.1|3008413_3009271_-|alpha/beta-hydrolase-fold-domain-containing-protein
MKRTLAPAIRLAILFLLPLAAFPSLASAQQKEKQSQEYKIDADVPYRSGDDLPESMQRCRLDVYYPVDRKDFATVVWFHGGGLTAGNKSIPQGLKNRGIAVVAVNYRLGPAVKSPAYIEDAAAAVAWTFNHIADYGGSRDRIYVSGHSAGGYLTSMVGLDRRWLAAHDIDANEIAGLIPFSGHTITHFTIRKERGIGGKQPVVDDLAPLYHVRKDAPPLLLITGDRELEMLGRYEENAYLWRMMQVVGHPNTELLELDGYDHGGMDDPAYPLMLKFIRKDLASKR
>NZ_CP036292.1|WP_145120375.1|3007546_3008233_-|carboxymuconolactone-decarboxylase-family-protein
MPSTARWPPVLQLTARDCAHPGLPQDKPQIDRQPSPSSFTPVFQAKERSTMPRLKTIGPNEAQPPLKEIYDDLTSQMGKVVNIFQGMGNSPAALKAYLSMSAALAEGDLSPEDREIIYLAVSEQNGCHYCVSAHAMLAKRVGLADDAIRAARQFQSSDPKHESLLTFVRRVIASKGFVSDEELQAVKSAGYSDGQIAEAVGYIGLATFSNLFNHVNGTELDFPAAEKI
>NZ_CP036292.1|WP_145124110.1|3005133_3005835_-|DUF1080-domain-containing-protein
MKDTNSTSISRDYTMQMNRLTRNTAVAAFSIFAALCSTVAVTAEENKSSGDEAAWISLFDGKSMEGWEKVGSDGSKWEVKEGAIWGSGTPSMLVNTTGPYKNFRYRAEVKINDGGNSGLYFRTTRRPGFSDGYEAQIDSTHTDPIRTGSLYGFCHVYPQLVKPGTWFTYEIEVRDDVWRGREMTRIKITVDGNELYEYLDFEKTYGPGHFAFQQHDPGSTVAIRQAEVQPLAD
>NZ_CP036292.1|WP_145120373.1|3004090_3004879_-|SDR-family-NAD(P)-dependent-oxidoreductase
MDLGLKNKLAVITGSTSGIGQAIAKSLLDEGATVVINGRSQTSLARATKELGGGDSLHGVAADVSTADGCAALVAAAEAIAPIDILINNAGIFEPKPFAEISDEDWQRFYEVNVMSGVRMSRAVMGSMQQRGWGRIVFISSESAINIPTEMVHYGMTKTAQLSISRGLAKTLKDTGVTVNCVLPGPTWSEGVEQFVESLAGEQDIEQVKRDFFRDSRGGSLIQRFASVEEVASLVSYVVSQRASATTGAALRCDGGLVDTCF
>NZ_CP036292.1|WP_145120392.1|3020077_3020803_+|hypothetical-protein
MTHSIWLSPTAIYLLLIGLSGLLGALVPEFYQWTGSDQSRMSPIVGWVAAGMAIVAAAIWSGLPFVTLRTEASASGLIRPIRFQLRTLFLWTTALAIGFAGLIRFPMPVSVFVCVAAYLHLAWFIARQQQHRWAAAALIGCMTLPYVWIAAPDGTNGIDVGWILLWMAGGMPMLFPAGFAASWLGQSLNDVGWLAIVMTAAQLVLGTWIIRLGPKRTIAYLIGCLLVSTFGSFCLHAMVLA
>NZ_CP036292.1|WP_145120394.1|3020855_3021506_-|hypothetical-protein
MAGYFLYSLDWPSLNSFLESPSEDLAAAMAENVSELLDSYDEQLEDDDEAADWPSDTESLLPILIDRLQRKDWYADLSEIGKNIWERAFVDLCNDDELNPFGFECESDGVYWNIVSEAIAHHDQPKNQLTEKEITHFGARPFRYWHSGRLNWDAWQPMHSMHSPAEVVALAEQFEAAEATLRDSRHPEVDEDYEELMSVLDKLKANGRVLYVSVDT
>NZ_CP036292.1|WP_145120396.1|3021552_3024162_+|hypothetical-protein
MEYNSASLWMLEVAMSRLMEPIEHVFVRHCLPAKHGDFERVKPLLRSGFDDSGSMSTAGLPALEACEANGRWTIAWEQAGSAWVLLDSNAAAAETLYRDNCKSRRSEVVWVRRAGDQFDFHWTAARKCVVDFRDYPGQPPIVKHDAANEAIAKCLQAGSGQEIFAALCKVAELLVPAESISVATQRFRIVPPRGRRARKSLRDFVIFSAPGLAPGENEAADRLAEAIDAGDVSALRQSIADGASLDQLPDRSLSPLLLALYRWGTTKSWRQCAQALIDAGCRIDPADGEPLVIEACSHLLSEQASVEILQLLIENGADLNARDRRGMTALDLSASRRRNQVVAFLIEHGADPTIETRQDQTIVDEIRNRVDQAAQYGKRSEYAETLELLTGVPYQVPDSLQLSDAVRSEAERFLSIVEARHLRKLLPKTVEIQPIKASRLNNFETFKPWCRELKQLGFVEACHVITCVALQVPQTILTDPQRRFDAILGDDGPLAPGGLRLEIVASAADGRIISVANKALQDDPRWRPTFLQSHVLEGRPVSELVDRMVELTKGIQLNEIAVDQAGDRYRGGVERLIDGMRQRTREVERSRIVDADGNVPRFERIGVYLQPRLGSQPDDLTSFSVAQSAERSFADDSGESKRSDPGRDLCETVRDAAVLAALDHLQMAGALHDESKIAAGIDAGMAFFQAFQDPSSEARDRWLAEPLCLILALASSRGQWDAVQAIAGGLSAEFLDASARFPDDPPVAMAEVLALVANRFGNQTSWDDSQLFASIAASRSKHAQLLAAVISAIDTADAPGFERAFTESLRHASKRKPRADWSFDLDRAVAWCETILWHLAAHRELPLPKLSEKQSDWLLCCEAPARGSD
>NZ_CP036292.1|WP_145120398.1|3024345_3025992_+|sulfatase-like-hydrolase/transferase
MKFSDTRVVGCKAFRQVVCIAIVAWGLVLGASPLAWSQSSREHAATTKSDATGKPNLVVIIADDMNWNDCGAYGHPAIRTPNIDRLASEGLLFQHAYLTTNSCSPSRASILTGRYPHNTAAEQLHWPLPAGTATLAEQLRRRGYYTAAAGKWHLGDAVRGDFDKIYEASTAGFVLPSGKDGEPPKMIAAQPSGCEDWERSLDDRPCDRPFFLWLAALDPHREYTAGALDPPHRSEDVIVPEHLPDTPEVREDLRLYYDEIGRLDGYVGKVLAKLKQQGVDENTLVLFISDNGRPFPRDKTTLYDGGIRTPWIVRWPARIAAGETTDALVSAVDIAPTFLQLADRATPAAGDSTQQTTRMSQNEGSQTAGVDVWQPEGKSFLATLLDPRKRHREFAFAEDHWHDYEDHARCVVDRRFKLIRNDYPDLPATPSADAGRGLTLQAMLKLQQRGELTAAQQSCFRSPRPRWELFDLQRDPSELVNRFDDPAYASVRDSMQQALLRWSQETGDYLPNRRTPDEFDRVSGAPDHSVRVRPRPSKQEMFGTNGKY
>NZ_CP036292.1|WP_145120400.1|3026988_3028158_+|TonB-dependent-receptor
MGTRNLLSGMLLAWGFCLTGGGAVTVAQETFDHVYRVADLDRDQGLVAAWSAGDSSDVQILSPGIDACAECTQCDSQGCDGCCATQECRSPWWAHRSGLFGEFLYLRPGDSDIVYSIEQNDTTVNAFPTGPLGIAAIDASPGYRVGFSLASSQTSSLVASYTHWDGNTQDRLVRNNANVLNSQIIHPSTFTTGGNSLQSSAATSIEFDLIDAVYRHKLICTDTTIFNWSGGFRYGTIEQSLLAQQEISVATGLVTVDTDVDFNGFGILLGCDAERRSCQSGMLCYSKGAASFLGGEWTGDYRQSNQFTGGIVANQYEDFRISPVLETELGIGWQSESGCVRATAGYMASWWCNAVSTREYVDGVRRGNYLEIDDTIAFIGLTTRLEVRY
>NZ_CP036292.1|WP_145120402.1|3028216_3028471_+|hypothetical-protein
MFAANASAANIAAVKNEWPAVVCTGDRRLAHLAGLGPAAFFSRVDRVKRSSWLCRNDLRLGLWSKKNAAEAAFVVINVSVLTRD
>NZ_CP036292.1|WP_145120404.1|3028691_3029768_-|DUF1559-domain-containing-protein
MVRFQKRSAKGFTLVELLVVIAIIGILVGLLLPAVQAAREAARRMSCSNNMKQLGLALHNYHDTYQSFPASAGVTLSTNASGQYDGWNSWSGLASILPFIEQGPLYDQIDFRYNFAANIAGVAEHSSVVRRTLLDAFLCPSDPGSDVSYTSDMAPSSYSFSHGPCTSWDVGNGSEPGVFDKAYFCRFRDITDGTSNTLAMAESKIGRNQGQWDSSNPNRDESYRVVVGTALRQSISGTNTTFRNTPAFITEINTYLDTCLGMYDSGSGWDGQSDEQNRWWAWGGAFRGPYVTTLRGPNAGPSCDNDASVTDISMKEASSNHPGGCMTLRADASVNFAGETTDQATWIALGSRAYGETL
>NZ_CP036292.1|WP_145120405.1|3030359_3032663_-|hypothetical-protein
MSKQTPGQRRNASRKPNVNAAPTSAESVPARGSFFSQIPLDVRAFAVWWLACCMLFIAANPTQIFDPIAVIPLPDNSVMAGADAWNPWLSTFDSLRSLFIWPTWLASVIAALLIAALGQRMVQRGEGVAAIAMVAGLCLIDPYDGLLAGWIVYAAVRLRDRMLAEPPLSHAMFFAIVGALSAAALASSLEATIPLLVLAVVVGTLILQSIRERRQTALVATLAAVLGLVAAGLIAWQHGLLAALLRPITAILNRPPATLLPSLSVSWQAPDFGWAHGLALLFILACWWRWVVARSPRMADGAMLAVFTALAIGSARYSWLATVAIACIASSQNFAASKPPSPTVARRWRRAACLVALLVLIAQVGLQRYDVLSALSSRRQIDPQQWNLAGPAVLQNLDRAANWQLQDDRGVHPLVVSDRWDAYGDFYPQYAMIVNDWSSWREHRYVRSDGQWGGFGEWFDQWNPKLVVIEAADLATIRQHSLDSPWKTLGIDSRRVIFAQIDDRDASGPLRESAQLLSILEIPRPAPNVDFERAIAFGGPTDARRIALVLSALRFPYAALRVLPNDNHLSTEFSRTMALLESAHRTLRFTGTPSLIDQSRALAHSERLLGRRDLTNQQRNQLQRAIDALQDVRQSSSLIVDVPAENDPALQSLEETAREQLMRGDFGAARQTTAKLGNNNTSLLLTTAATLSMSPPESILAALQSADSDHDSGRSDGLAELLFYRGLLRLETGDFRGALQDFTRSLNSTPSPPQRDLISAFCSQIAN
>NZ_CP036292.1|WP_145120406.1|3032659_3033781_-|hypothetical-protein
MSETNKSTDKRTPLAARIAVVAIALLVAAASLTSSRDPVPGDAVLTLNGWADETSCRECHFEADSYPETGHAQTLRPATDPRSIEILSSVNSDASAADDGLQIDIDPESGVFAVQQDQEISRRIRLDWCFGSGAHAHTWTSTVGDLLGNTDELEFRWTWFHQTNSFALTPGQPEQAGDSHYGAFGLFFDGAKAVGCFSCHTSYLPAENGSIDFHGMVAGINCQRCHGPQQAHVASGGEVIDSDWMATDRLDAVRRCGQCHRNADEQPPGEIRTDNPGIVRFQPVGLLQSPCFIKSEMSCTTCHDPHKSLAAQDSRGIWQCVQCHNPDSPTHTLCAADNRDDCLRCHMPKVATNPNIRFTDHWIRVRDDIEESK
>NZ_CP036292.1|WP_145120407.1|3033889_3036103_-|1,4-alpha-glucan-branching-protein-GlgB
MHTQVPLDGIGRLVAGRHENPAELLGPHPVEYQGRKAIAVRAFVPDSTQVWLVDQPEDAPRPMRRLHPAGFYEAICPVDNEALSSNYRLKVARNSGEVTIMPDPYAVEPLLQELDRYLLGEGRHYELYKRLGAQIRTVGDTSGVNFSVWAPNAKTVQVVGDFNEWDGAQHAMKVHPNLGVWELFIPGVKAGDIYKYRILQQDGHWNDKSDPLGFAAELPPRTASVVTELDTHTWQDDAWMETRRESNQLEKPFNIYEVHLGSWQQGGEQEHGWLNYRELAHRLVAYCQEMNFTHLELMPISEHPYTGSWGYQTVGYFAATSRYGTPEDFMYFVDYCHQNGIGVILDWVPAHYPKDGHGLANFDGSALYEHADPRQGEHPDWGTKIFNYGRNEVRNFLISNALFWLDKYHIDGLRVDAVASMLYLDYSREDGEWIPNEHGGRENIAAIDFLREFNVVVHEKYPGAVTIAEESTAWGGVSRPTYEGGLGFTFKWNMGWMNDTLDYFHNDPIHRSHHHDALTFSLIYAFTENFTLPLSHDEVVHGKGALLAQMPGDLWQKFANLRLLYSYMWTHPGKKLLFMGGEFGQWNEWNEDDPIQWELLDFDTHRGIQNLVRDLNQLVVENPALHHDDFTAAGFEWVDCMNAQDSVLAYVRKADGFGPALMVCANFTPVVRKGYHVGVTQSGRWTEIFNSDAEIYGGSNIVNPGMTQSLGIPHHGRTDSIKIDLPPLGIVVLKHES

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Crispr_ID: NZ_CP036292_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_15

4093580-4093662

Orphan

Consensus_repeat	Method
ATTTTGAGGGTGTCCCCTATCGCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_15

>merge|NZ_CP036292|15|4093580-4093662|CRISPRCasFinder
ATTTTGAGGGTGTCCCCTATCGCGTCCCCTATCGCGCTATATCGCGCCTATCGCGCGCTATTTTGAGGGTGTCCCCTATCGCG

>NZ_CP036292|15|15|4093580-4093662|CRISPRCasFinder
ATTTTGAGGGTGTCCCCTATCGCG	TCCCCTATCGCGCTATATCGCGCCTATCGCGCGCT
ATTTTGAGGGTGTCCCCTATCGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145121750.1\|4097974_4099711_-\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036292.1\|WP_145121725.1\|4081005_4081812_+\|type-1-glutamine-amidotransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|153235
NZ_CP036292.1\|WP_145121732.1\|4085573_4086935_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|308197
NZ_CP036292.1\|WP_145121746.1\|4096153_4097410_-\|GTP-binding-protein	unknown	unknown	gnl\|CDD\|223597
NZ_CP036292.1\|WP_145124165.1\|4095506_4096139_-\|MerC-family-mercury-resistance-protein	unknown	unknown	gnl\|CDD\|377004
NZ_CP036292.1\|WP_145121742.1\|4093913_4094624_+\|cobalt-transporter	unknown	unknown	gnl\|CDD\|225125
NZ_CP036292.1\|WP_145121734.1\|4087194_4087422_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121736.1\|4088310_4088532_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121744.1\|4094740_4095358_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121740.1\|4089960_4091127_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121756.1\|4102204_4102891_-\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|131644
NZ_CP036292.1\|WP_145124163.1\|4091511_4091826_+\|cation-transporter	unknown	unknown	unknown
NZ_CP036292.1\|WP_145124166.1\|4105233_4106595_+\|terpene-cyclase/mutase-family-protein	unknown	unknown	gnl\|CDD\|238362
NZ_CP036292.1\|WP_145121754.1\|4101154_4101880_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|214906
NZ_CP036292.1\|WP_145121727.1\|4082134_4083037_-\|DUF547-domain-containing-protein	unknown	unknown	gnl\|CDD\|368117
NZ_CP036292.1\|WP_145124164.1\|4092398_4093391_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121748.1\|4097406_4097817_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121729.1\|4083084_4085490_-\|4Fe-4S-binding-protein	unknown	unknown	gnl\|CDD\|188533
NZ_CP036292.1\|WP_145121738.1\|4088528_4089635_+\|inorganic-phosphate-transporter	unknown	unknown	gnl\|CDD\|223383
NZ_CP036292.1\|WP_145121752.1\|4100005_4100437_+\|transcriptional-repressor	unknown	unknown	gnl\|CDD\|223806

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145121750.1\|4097974_4099711_-\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	1.8747e-13
NZ_CP036292.1\|WP_145121725.1\|4081005_4081812_+\|type-1-glutamine-amidotransferase-domain-containing-protein	gnl\|CDD\|153235	cd03141, GATase1_Hsp31_like, Type 1 glutamine amidotransferase (GATase1)-like domain found in proteins similar to Escherichia coli Hsp31 protein. Type 1 glutamine amidotransferase (GATase1)-like domain found in proteins similar to Escherichia coli Hsp31 protein (EcHsp31). This group includes EcHsp31 and Saccharomyces cerevisiae Ydr533c protein. EcHsp31 has chaperone activity. Ydr533c is upregulated in response to various stress conditions along with the heat shock family. EcHsp31 coordinates a metal ion using a 2-His-1-carboxylate motif present in various ions that use iron as a cofactor such as Carboxypeptidase A. The catalytic triad typical of GATase1 domains is not conserved in this GATase1-like domain. However, in common with a typical GATase1 domain, a reactive Cys residue is found in the sharp turn between a beta strand and an alpha helix termed the nucleophile elbow. For EcHsp31, this Cys together with a different His and, an Asp (rather than a Glu) residue form a different catalytic triad from the typical GATase1 domain. For Ydr533c a catalytic triad forms from the conserved Cys together with a different His and Glu from that of the typical GATase1domain. Ydr533c protein and EcHsp31 are homodimers.	4.39665e-112
NZ_CP036292.1\|WP_145121732.1\|4085573_4086935_-\|hypothetical-protein	gnl\|CDD\|308197	pfam02450, LCAT, Lecithin:cholesterol acyltransferase. Lecithin:cholesterol acyltransferase (LCAT) is involved in extracellular metabolism of plasma lipoproteins, including cholesterol.	1.64609e-05
NZ_CP036292.1\|WP_145121754.1\|4101154_4101880_-\|hypothetical-protein	gnl\|CDD\|214906	smart00910, HIRAN, The HIRAN protein (HIP116, Rad5p N-terminal) is found in the N-terminal regions of the SWI2/SNF2 proteins typified by HIP116 and Rad5p. HIRAN is found as a standalone protein in several bacteria and prophages, or fused to other catalytic domains, such as a nuclease of the restriction endonuclease fold and TDP1-like DNA phosphoesterases, in the eukaryotes. It has been predicted that this protein functions as a DNA-binding domain that probably recognises features associated with damaged DNA or stalled replication forks.	4.82755e-13
NZ_CP036292.1\|WP_145124165.1\|4095506_4096139_-\|MerC-family-mercury-resistance-protein	gnl\|CDD\|377004	pfam03203, MerC, MerC mercury resistance protein.	1.82835e-21
NZ_CP036292.1\|WP_145121742.1\|4093913_4094624_+\|cobalt-transporter	gnl\|CDD\|225125	COG2215, COG2215, ABC-type uncharacterized transport system, permease component [General function prediction only].	4.02071e-17
NZ_CP036292.1\|WP_145121756.1\|4102204_4102891_-\|PEP-CTERM-sorting-domain-containing-protein	gnl\|CDD\|131644	TIGR02595, conserved_hypothetical_protein, PEP-CTERM protein-sorting domain. This model describes a 25-residue domain that includes a near-invariant Pro-Glu-Pro (PEP) motif, a thirteen residue strongly hydrophobic sequence likely to span the membrane, and a five-residue strongly basic motif that often contains four Arg residues. In nearly every case, this motif is found within nine residues, and usually within five residues, of the extreme C-terminus of the protein. Proteins with this motif typically have signal sequences at the N-terminus. This region appears many times per genome or not at all, and co-occurs in genomes with a proposed protein-sorting integral membrane protein we designate exosortase (see TIGR02602). PEP-CTERM proteins frequently are poorly conserved, Ser/Thr-rich proteins and may become extensively modified proteinaceous constituents of extracellular material in bacterial biofilms. [Cell envelope, Surface structures].	0.000447972
NZ_CP036292.1\|WP_145121746.1\|4096153_4097410_-\|GTP-binding-protein	gnl\|CDD\|223597	COG0523, COG0523, Putative GTPases (G3E family) [General function prediction only].	8.19668e-113
NZ_CP036292.1\|WP_145124166.1\|4105233_4106595_+\|terpene-cyclase/mutase-family-protein	gnl\|CDD\|238362	cd00688, ISOPREN_C2_like, This group contains class II terpene cyclases, protein prenyltransferases beta subunit, two broadly specific proteinase inhibitors alpha2-macroglobulin (alpha (2)-M) and pregnancy zone protein (PZP) and, the C3 C4 and C5 components of vertebrate complement. Class II terpene cyclases include squalene cyclase (SQCY) and 2,3-oxidosqualene cyclase (OSQCY), these integral membrane proteins catalyze a cationic cyclization cascade converting linear triterpenes to fused ring compounds. The protein prenyltransferases include protein farnesyltransferase (FTase) and geranylgeranyltransferase types I and II (GGTase-I and GGTase-II) which catalyze the carboxyl-terminal lipidation of Ras, Rab, and several other cellular signal transduction proteins, facilitating membrane associations and specific protein-protein interactions. Alpha (2)-M is a major carrier protein in serum and involved in the immobilization and entrapment of proteases. PZP is a pregnancy associated protein. Alpha (2)-M and PZP are known to bind to and, may modulate, the activity of placental protein-14 in T-cell growth and cytokine production thereby protecting the allogeneic fetus from attack by the maternal immune system.	9.19012e-15
NZ_CP036292.1\|WP_145121727.1\|4082134_4083037_-\|DUF547-domain-containing-protein	gnl\|CDD\|368117	pfam04784, DUF547, Protein of unknown function, DUF547. Family of uncharacterized proteins from C. elegans and A. thaliana.	1.21611e-25
NZ_CP036292.1\|WP_145121729.1\|4083084_4085490_-\|4Fe-4S-binding-protein	gnl\|CDD\|188533	TIGR04018, thioredoxin_reductase, putative bacillithiol system oxidoreductase, YpdA family. Members of this protein family, including YpdA from Bacillus subtilis, are apparent oxidoreductases present only in species with an active bacillithiol system. They have been suggested actually to be thiol disulfide oxidoreductases (TDOR), although the evidence is incomplete. [Unknown function, Enzymes of unknown specificity].	2.11812e-43
NZ_CP036292.1\|WP_145121738.1\|4088528_4089635_+\|inorganic-phosphate-transporter	gnl\|CDD\|223383	COG0306, PitA, Phosphate/sulphate permeases [Inorganic ion transport and metabolism].	5.78904e-51
NZ_CP036292.1\|WP_145121752.1\|4100005_4100437_+\|transcriptional-repressor	gnl\|CDD\|223806	COG0735, Fur, Fe2+/Zn2+ uptake regulation proteins [Inorganic ion transport and metabolism].	1.31774e-20

>NZ_CP036292.1|WP_145124164.1|4092398_4093391_-|hypothetical-protein
MCGEDPYTGQSFQHRRGWIRERLEFLASCFAIDCLTFSIMSNHLHLVLRSRPDVVAVLSDEEVARRWLRLFPVRCNDDGSPAEPSDAEIASIVNNEQVLAQRRRRLSDISWWMRCTAENIARRSNAEDDVNGHFWEGRYKAQLILDEASLLACAAYVDLNPIRAAIVETIEASEFTGAKERVDDITCASEQNRKHGHDWERSRIPHHSGWMSPVEIDERDDPIGADIDSSHRRSSCKGFLSISLSKYLELLDWTGRQLRDDKRGSIPAELAPILTRIGIDAPTWCDLVKRFGRLFKRAAGTSESLCKEAARRRQAWMQAPGNPLVGPAPP
>NZ_CP036292.1|WP_145124163.1|4091511_4091826_+|cation-transporter
MLAALLVSSQAHADEKKVTTTTVTVGEMCGGCVKKITARFDKEKAIARVTCDIDKKTTVLTPAKGVRLSPKGVWEIFESIGKTPEKLVGPKGTFTSKPKARLQD
>NZ_CP036292.1|WP_145121740.1|4089960_4091127_+|hypothetical-protein
MSEYQYVVFRAIDRPLDDKQLAFAEKQSSHSELSQWEMSVEYHYSSFRGDVDGLLRRGFDVHLAYANYGYREIRLRLPSGLPLPASIIPAFLFCDGLQWKQDAKGNGGILSVAPFHESGEIEEVWDFDDYLNSLAKIREQLIGGDLRALYLLWLCAAYDDNEEPEEMVEPPVPHGLDKMPALSTELLPFFGHDPLILKAAAEGVPGFDPNNSDEDPVQDWVQSITEARSRALLQRLLKEDPVSVKAELLAELRESGSIDDWPTMVRGRTLDELLDATAEQREEANRIQKKKDQAKAKRAAAKAEKERQARMDKMKSAPKTWLAEAEEIANTGGTANYKAAADILADLREAIGGDRGDQLARDCATKLAKDNPTLNMLKSALRKRGLFG
>NZ_CP036292.1|WP_145121738.1|4088528_4089635_+|inorganic-phosphate-transporter
MIVLLALVAGVLLAYANGANDNFKGVATLYGSDTTTYRRALVWATVTTAAGSLTAVWLARELLERFSGKGIVPDALVAQNEFGVAVALAAGVTVMLASRLGFPISTTHALVGSMVGAAGASSFAVDWNVLSTKLMAPLLLSPLIAILVTAVLYLTFRRTRIAMGITKETCLCSGREVVEVVPLGSCAMSMSRAEELSIRLGTNVSCRDHYAGNLVGVDARQTLDTMHFLSAGMVSFARGLNDTPKIAALLLIVPALNSLTATVVCGAAIGIGGWFGAKKIAEKLSHGITEMNAGQGFSANLVTSILVVFASRWGLPVSTTHVSCGALFGIGSLTGQANWKSIAHILLAWVTTLPAAALIGWLVFNILT
>NZ_CP036292.1|WP_145121736.1|4088310_4088532_+|hypothetical-protein
METELSSDRDQQVAGASVKQQHAASHHPVAPTQSLRVELSPHVLAAMPEAITEGDCGCGASRQEAVDRIGVAQ
>NZ_CP036292.1|WP_145121734.1|4087194_4087422_+|hypothetical-protein
MANTAQAAGMGLSFVHGCIIEVVRDQLKETVAEATFPSIRSAMCERMPGFRYAIRYSVAIGMHVANHRIRRLPSL
>NZ_CP036292.1|WP_145121732.1|4085573_4086935_-|hypothetical-protein
MIVIPGVLGSRLVDEETGKIVWGKYDKIRFRRQQSEDLAEVSLPMAQGVPLSQLRDSVRSDGTLAYLELSVFGIPVELQAYNQILQTLGVGGYRDSSAPKSDEFNYGDEHFTCFQFDYDWRRDVAENAALLDRFIAEKREYIRAEYANRYGITDTEIRFDIVAHSLGGLLSRYYLRYGSQQLPDDGSLPTLDWEGARNVERLVMVGTPNAGSAFALRDLVNGHQLSRVLPYYPPAALGTMPSIYQMLPRPRHQTLVDAKNSDQAYDFYDPDLWRQMKWGLADPNQDDILQELLPDVADREARECIALDHQRKCLLKAKQFHQSLDIPATPPPGVTLHLYAGDAIETPAVMSVDMETGQLEVAHSVPGDDTTTRHSAVMTEQPVDAVSTRPASPIRWDSVTFLHTSHRKLTADPVFTDNVLALLLQSPRHDQTPIHSPSSVGASVHRQQLERIP
>NZ_CP036292.1|WP_145121729.1|4083084_4085490_-|4Fe-4S-binding-protein
MAANASKSDRKKTSYFATVPPQEILPIVNSRYESSVKGIYVIGDVTGLPLVKVAANQGASVIAKMKFDDGSAADDGRLDLVIIGAGPAGLSAAMEAQERGLKYVVLERNKIASTVRSFPPGKKVYAEPQFVRNESKLDFDEDLDKDDFLARVNRLVAEKKLHIKEATEVDRVRKVGERRFEVETKSGKSFPTQQVLVAVGRQGQARLLECPGADNAAKVTYRLHTPEDYNDADIMVVGGGNSAIEAALLLMPHNRVTLSYRGDDLFRAKEENRQLIEQAQRDGRLNILYKSNLKAIRDDEVDIDVDGQSHTLANDHVIVQIGTLPPVDFLIDMGLELDGVWTGKRLALSVVGLLVGIIVYFYSKNFVFHPDAAGEGKLLLPGLESIVGPTQLGFAAFLTGTVLPIAWLSLLALKLINGNMQARGRAALLPIPHSTFMLIAGGLLYAGSLVAPDVLTLDPSAAGDGPYFVPGFTWLYNVVPKYFSNAYGLYYLVYFSAIAGFGLYWAIKANHRLIWRRNLTIIATQWTLWWGIPTFLVVFIGRNPWTPLLTRSLNAWPLNMGAFNVDPVVGPGDPAWWHTVAVVGVVWAAVLTFIMIPLVTIRWGKIYCSYICSCGALAETVGNGFRHRGPKGDTPRKIERMGFIFIALATVATIADLYGFEGPLGQYNLWVGTALAGAVAIGLYPFLGQRVWCRMWCPLAFWMNFWGRWSQFKITPEKGKCIDCNVCNQYCQMGIDIKSSALKGEPITLEDSPCVGCNECIVRCPMEILHLGDLPIAKQNASASLPIVNSPLIKPRKREIV
>NZ_CP036292.1|WP_145121727.1|4082134_4083037_-|DUF547-domain-containing-protein
MNKSKASYYGPFFWLAIVSFSVPIVVAAKAFQEVQLSTKPTPHPDASGVDHALWDYLLKTHVENGLVDYDGIARDHLFRTYLRQLSESEPSKLTTSADQLALFCNAYNAFVINGVITHKIRDSVMNYNVEGTEFFDLKEHILYGETFSLNEIEHELIRKRFREPRIHVALVCAAKSCPAIRAEAYTGPRLTKQLEDQSIQFANQTKYVTYDAASDTLRLSPLLDWYGGDWDPVGGYLPWLADRVEDDGVKQAILRASRNETSVAFLDYDWSLNSQAADGSAAPKPASRKGQFGSGSIPNE
>NZ_CP036292.1|WP_145121725.1|4081005_4081812_+|type-1-glutamine-amidotransferase-domain-containing-protein
MSRSITTGTLLLATFALLISGCKNELGQSQTDTEIQKSTAKKVLFVVTSHDEKGDTGEKTGYYLGEVTHPWEVLHSAGYEIDFVSPKGGKAPVDAFDMSDPINKKFWDDDVYRNKVENTKTPREVNPDDYVAIHYAGGHGAMWDFAGNDAIAEIAAKIYENNGVVSAVCHGPAGLVNIKLSDGTYLVDGKKVNAFTNEEEVKVELDEVVPFLLEDKLIERGAQFEKSEPFQEHVAVDQRLVTGQNPQSATGVGMATLKELQKLNEATQ
>NZ_CP036292.1|WP_145121742.1|4093913_4094624_+|cobalt-transporter
MHQHTHELTLGVAFFLGALHALEPGHGKTAMLVYLSGERRSYWHPLVMGLSSGLAHSVSLIAIAMAVHLTHHLITGDHHHDNEAMTATLQWISAGLVLCVGTWMLWAAYRAKPAKKCGCRHHRDEDCDAKPPSAKSSYSMSALLGVAFGLLPCPSALAAYFTSMSTGSPVAAYAVIGLFAAGIASSLTCVGMLLQRFGGSLIREESRLAKLPWSYIRAILILGVGLFYAARVAMAG
>NZ_CP036292.1|WP_145121744.1|4094740_4095358_-|hypothetical-protein
MIDRVWATGLLSQQIWCWGQDVKRPEGNWLLEIGFERTTPPEHRKECSSVYTLAINDRTRITLRGFGIYIGDDLRGGMFIERYGFTPKYSSKSRLDCPPWSTNDLPDFQFPDAQQRDPTAMLLLDLLDWIRQYELEVVKRLGIDYRRNTLMQWNNGKRPFIPAEQMASSWRELTIAIAANPDAWISLNADQPISSGNRAEEGSEQ
>NZ_CP036292.1|WP_145124165.1|4095506_4096139_-|MerC-family-mercury-resistance-protein
MQPTSIGPRGSEPRLADSSSATFGWQDWIGIVASIGCAIHCAAMPFVIAFLPALGLSFLADEGFHRWMALACFVIALAAFVPGFRKHRRWTPGAIAIVGLSLITFAAFGFAGDCCAACESPAGTEVAATACADACCEHCAVNATAETKSSNPSNASFVTASVVSPNFLTGIAPWITPLGGILLVSAHLLNRRYGCLCGCCEAKPAAKVAE
>NZ_CP036292.1|WP_145121746.1|4096153_4097410_-|GTP-binding-protein
MNPSVSTKRLPVTVLSGFLGAGKTTLLNHILTNRDNLKVAVIVNDMSEVNIDAALVKSGDANLSRTEEQLVEMSNGCICCTLREDLLVEVRRLARDGRFDYLLIESTGISEPLPVAETFTFEDEEGESLSMIAELDTMVTVVDAGNFMKDFGSWDDLADRRMGLSEDDTRNIVDLLVDQVEFANVIIVNKTDLISPYDLEQLNRILRKLNAKAKILNTTESRCELAEIMGTGLFSLDEAEAQPEWLAVPRGQEETETEEYGISSFVYRSERPFHPKRLTEALDGDMDDGLFSGVLRSKGLMWIASRHDWAYDWSQAGCSIRMNPAGFWWAAAPDDAWPDDESLVAEIRSKFVGEHGDRHQELVFIGNAMDPQRITNILDACLLTDLEFTQGPELWANFEDPLPGIELEPGEELMEEEV
>NZ_CP036292.1|WP_145121748.1|4097406_4097817_-|hypothetical-protein
MFRLSLLAAVIVCLLGAQLRGDDPSALLIATSHQRTASSLPPLPHGSRVVVLIQDSEDDYATVNARALRARDATHIVFDRAEQSPLVTLFCERLTIRGAIPIGLHKPSSQPLDLAKSIKDASTQTSFANFFAGPQQ
>NZ_CP036292.1|WP_145121750.1|4097974_4099711_-|PQQ-binding-like-beta-propeller-repeat-protein
MHTACTCSAMRELVDSSFSSRKSTVMIPAPFHGFSQAASFLRGLAVLSIGLMFSSTGFLRADDAVGSWSSFRDGGASRASSALPTRWSASEGIAWQKELEGYGQSAPVIHAGKVIVTSVIGPNCQQIAVDCLDFATGQAAWSYRRASSNEHPSNYMNARAAPTPIVDEAGVYAFFETGDFVALDWEGEMIWHRDETETSGKFDNSHGIGASPASDATSLYLLIEHGGPSSLSAINKTDGSVRWSIERDSTKSWASPVIATVDGRSQVIVSSGGTVTGYDTADGSEVWQLDGVEGNSVPSPVVDGERLIVAARLPEFSSDGQVRANCAVDLSRLKDGKPEVLWRAEKAISEYASPVVCGEFVYFLNKANVLHCIDIATGEIAYRKRLSLACWATPIVAGDLVYFFAKSGETKVVRAGPTYEELAVNALWDVSNPPAPLHYRESQGGHGGHGGGGAPGAHAKEAIPTKESPVGGHGGEGPKKAPGGGMVARMMAGDANGDGVLEGEEVPEMFRAMIGRIDTDGDGRIDADELEAMAKSFAERRKDSAASARDPIVYGVAAADGRIAIRTGTRLYVVAHDH
>NZ_CP036292.1|WP_145121752.1|4100005_4100437_+|transcriptional-repressor
MSQHDESLDLVKQAIRDAGLRATPARIATLQLLRRSSQPLTHSAVVEGLADVNVDKATVFRSLNDMAEVKLVRRTQVGDHVWRFEAIDPNDEHDTGHPHFLCVDCGTVSCLSDVKLTAGSQRASEAVGEVTQILLQGHCNDCK
>NZ_CP036292.1|WP_145121754.1|4101154_4101880_-|hypothetical-protein
MAANESALAMADVTWFEIATLKRPAVIPLGGDNYLKEIGTGTAFLTTKQVSMIGELQSKKFVLNSVQRVTRYADGILFNRSSGKSVFLKTPMLSELSARFGLVAEYTCSGEPVLGVSPSSNFIPNIVDAEVIEPMTTHPNRNRNADSDPRYTFRVVGDFVGNRESHIRRLRVGDQIWLVKEPSNVHDPHAVAVFDVTRNQLGYLKRDVASWFSPLLGRKTNIEARVHCFTSEGALIVGVYC
>NZ_CP036292.1|WP_145121756.1|4102204_4102891_-|PEP-CTERM-sorting-domain-containing-protein
MNLLLNSSSTRGYIQGNEMRRFVLAIACIAMTVVMAEELHAGVIITYYDNGEDLFFDYAGSLDADTGTIIPGKRSVVSHIGASQTVFFSAVGGFGFVGNDNGASHTPGLFATNIRADYVDEDGFSSGTGFMFGVLHGIDGSTVSMNLWGDWGLPNTAINGRLVLPGQTVLGIGMVDGWSAQTDWGTITFRDAASVSTVPEPTSLAIFGIGALSLVASRRRRKDKVDLV
>NZ_CP036292.1|WP_145124166.1|4105233_4106595_+|terpene-cyclase/mutase-family-protein
MLEVEKSAPAWLISLVVHLVALLLLALLTLPSTVGVGRLMIELGVSEEQEEIDLATFELDSTDVPDTLETAEMSELAEVQVDDSFAPMEMSEFIAPVEVGPITAELSVGSALTGRTGAMKQALLATHGGTPATQNAVQMGLEWLKRNQQRGGFWSLSGRYSDGSSTENKPAATAMALLAFQGDGHTHLSGEFKEQVHDGIKWLVNHQDREGSFVTKSQVPSHQALYAQGQCMIAICELYAMTKDSWLREPAQRAVNYAVEIQSKEGGWRYYPRRESDTSVTGWFLMGLKSAQMSDLVVPTSTMANIEKYLDTVSHYDGSAYSYQPNSPPSRAMTAEGLLCRQYLGWEGDNPALQEAVITIDENYPFNFEDRDFYYWYYATQVLHHYGGTPWRNWNSVMREELPKAQVASGREAGSWAPQGSRWGSSGGRLYTTCLSLFCLEVYYRHLPLYGNK

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Crispr_ID: NZ_CP036292_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_16

4310720-4310811

Orphan

Consensus_repeat	Method
CGGCCTAGGGATTGGTGGTTCTGC	CRISPRCasFinder

1 spacers

DinG

The CRISPR arrays of NZ_CP036292_16

>merge|NZ_CP036292|16|4310720-4310811|CRISPRCasFinder
CGGCCTAGGGATTGGTGGTTCTGCGGGTACCGGCGGCTGACACCGCCGGCAGTTGGTGTGTCGGCCTGCGGCCTAGGGATTGGTGGTGCTGC

>NZ_CP036292|16|16|4310720-4310811|CRISPRCasFinder
CGGCCTAGGGATTGGTGGTTCTGC	GGGTACCGGCGGCTGACACCGCCGGCAGTTGGTGTGTCGGCCTG
CGGCCTAGGGATTGGTGGTGCTGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145121994.1\|4316172_4317621_-\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|369346
NZ_CP036292.1\|WP_145121983.1\|4305969_4309389_-\|acyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|274311
NZ_CP036292.1\|WP_145122004.1\|4324565_4325486_+\|dihydrodipicolinate-synthase-family-protein	unknown	unknown	gnl\|CDD\|188630
NZ_CP036292.1\|WP_145121998.1\|4320967_4321852_-\|FCD-domain-containing-protein	unknown	unknown	gnl\|CDD\|224715
NZ_CP036292.1\|WP_145121979.1\|4302043_4302922_-\|pyruvate-kinase	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121986.1\|4311215_4311668_-\|IS200/IS605-family-transposase	unknown	unknown	gnl\|CDD\|376616
NZ_CP036292.1\|WP_145121988.1\|4312364_4314137_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|163503
NZ_CP036292.1\|WP_145121978.1\|4300245_4301538_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036292.1\|WP_145121981.1\|4303334_4304351_+\|RNA-3'-terminal-phosphate-cyclase	unknown	unknown	gnl\|CDD\|235255
NZ_CP036292.1\|WP_145121974.1\|4295834_4297856_-\|helicase	DinG	COG1199_DinG_CAS-IV-A	gnl\|CDD\|236148
NZ_CP036292.1\|WP_145121992.1\|4314910_4315906_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145121990.1\|4314332_4314788_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121972.1\|4294286_4295780_+\|glycogen-synthase-GlgA	unknown	unknown	gnl\|CDD\|234809
NZ_CP036292.1\|WP_145124184.1\|4304382_4305780_+\|RtcB-family-protein	unknown	unknown	gnl\|CDD\|376465
NZ_CP036292.1\|WP_145121984.1\|4309410_4310406_-\|SMP-30/gluconolactonase/LRE-family-protein	unknown	unknown	gnl\|CDD\|225921
NZ_CP036292.1\|WP_145121970.1\|4290720_4294011_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145122000.1\|4322009_4323188_+\|galactonate-dehydratase	unknown	unknown	gnl\|CDD\|239441
NZ_CP036292.1\|WP_145122002.1\|4323187_4324582_+\|alkaline-ceramidase	unknown	unknown	unknown
NZ_CP036292.1\|WP_145121976.1\|4298250_4299981_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370676
NZ_CP036292.1\|WP_145121996.1\|4317651_4320957_-\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377872

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145121994.1\|4316172_4317621_-\|DUF1501-domain-containing-protein	gnl\|CDD\|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	3.41011e-137
NZ_CP036292.1\|WP_145121983.1\|4305969_4309389_-\|acyltransferase-domain-containing-protein	gnl\|CDD\|274311	TIGR02813, omega-3_polyunsaturated_fatty_acid_synthase_PfaA, polyketide-type polyunsaturated fatty acid synthase PfaA. Members of the seed for this alignment are involved in omega-3 polyunsaturated fatty acid biosynthesis, such as the protein PfaA from the eicosapentaenoic acid biosynthesis operon in Photobacterium profundum strain SS9. PfaA is encoded together with PfaB, PfaC, and PfaD, and the functions of the individual polypeptides have not yet been described. More distant homologs of PfaA, also included with the reach of this model, appear to be involved in polyketide-like biosynthetic mechanisms of polyunsaturated fatty acid biosynthesis, an alternative to the more familiar iterated mechanism of chain extension and desaturation, and in most cases are encoded near genes for homologs of PfaB, PfaC, and/or PfaD.	1.40207e-36
NZ_CP036292.1\|WP_145122004.1\|4324565_4325486_+\|dihydrodipicolinate-synthase-family-protein	gnl\|CDD\|188630	cd00408, DHDPS-like, Dihydrodipicolinate synthase family. Dihydrodipicolinate synthase family. A member of the class I aldolases, which use an active-site lysine which stabilizes a reaction intermediate via Schiff base formation, and have TIM beta/alpha barrel fold. The dihydrodipicolinate synthase family comprises several pyruvate-dependent class I aldolases that use the same catalytic step to catalyze different reactions in different pathways and includes such proteins as N-acetylneuraminate lyase, MosA protein, 5-keto-4-deoxy-glucarate dehydratase, trans-o-hydroxybenzylidenepyruvate hydratase-aldolase, trans-2'-carboxybenzalpyruvate hydratase-aldolase, and 2-keto-3-deoxy- gluconate aldolase. The family is also referred to as the N-acetylneuraminate lyase (NAL) family.	2.52719e-42
NZ_CP036292.1\|WP_145121996.1\|4317651_4320957_-\|DUF1553-domain-containing-protein	gnl\|CDD\|377872	pfam07583, PSCyt2, Protein of unknown function (DUF1549). A family of paralogues in the planctomyces.	1.74293e-90
NZ_CP036292.1\|WP_145121986.1\|4311215_4311668_-\|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.	8.47442e-31
NZ_CP036292.1\|WP_145121988.1\|4312364_4314137_-\|hypothetical-protein	gnl\|CDD\|163503	TIGR03791, TTQ_mauG, tryptophan tryptophylquinone biosynthesis enzyme MauG. Members of this protein family are the tryptophan tryptophylquinone biosynthesis (TTQ) enzyme MauG, as found in Methylobacterium extorquens and related species. This protein is required to complete the maturation of the TTQ cofactor in the methylamine dehydrogenase light (beta) chain.	2.4114e-13
NZ_CP036292.1\|WP_145121978.1\|4300245_4301538_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.16437e-31
NZ_CP036292.1\|WP_145121981.1\|4303334_4304351_+\|RNA-3'-terminal-phosphate-cyclase	gnl\|CDD\|235255	PRK04204, PRK04204, RNA 3'-terminal phosphate cyclase.	2.22962e-156
NZ_CP036292.1\|WP_145121974.1\|4295834_4297856_-\|helicase	gnl\|CDD\|236148	PRK08074, PRK08074, bifunctional ATP-dependent DNA helicase/DNA polymerase III subunit epsilon; Validated.	1.39349e-151
NZ_CP036292.1\|WP_145121992.1\|4314910_4315906_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	1.36413e-55
NZ_CP036292.1\|WP_145121998.1\|4320967_4321852_-\|FCD-domain-containing-protein	gnl\|CDD\|224715	COG1802, GntR, Transcriptional regulators [Transcription].	6.42607e-22
NZ_CP036292.1\|WP_145121972.1\|4294286_4295780_+\|glycogen-synthase-GlgA	gnl\|CDD\|234809	PRK00654, glgA, glycogen synthase GlgA.	0
NZ_CP036292.1\|WP_145124184.1\|4304382_4305780_+\|RtcB-family-protein	gnl\|CDD\|376465	pfam01139, RtcB, tRNA-splicing ligase RtcB. This family of RNA ligases (EC:6.5.1.3) join 2',3'-cyclic phosphate and 5'-OH ends. They catalyze the splicing of tRNA and may also participate in tRNA repair and recovery from stress-induced RNA damage.	3.78837e-117
NZ_CP036292.1\|WP_145121984.1\|4309410_4310406_-\|SMP-30/gluconolactonase/LRE-family-protein	gnl\|CDD\|225921	COG3386, COG3386, Gluconolactonase [Carbohydrate transport and metabolism].	1.07514e-60
NZ_CP036292.1\|WP_145121970.1\|4290720_4294011_-\|hypothetical-protein	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.	4.80698e-23
NZ_CP036292.1\|WP_145122000.1\|4322009_4323188_+\|galactonate-dehydratase	gnl\|CDD\|239441	cd03325, D-galactonate_dehydratase, D-galactonate dehydratase catalyses the dehydration of galactonate to 2-keto-3-deoxygalactonate (KDGal), as part of the D-galactonate nonphosphorolytic catabolic Entner-Doudoroff pathway. D-galactonate dehydratase belongs to the enolase superfamily of enzymes, 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.	1.33662e-137
NZ_CP036292.1\|WP_145121976.1\|4298250_4299981_+\|hypothetical-protein	gnl\|CDD\|370676	pfam09770, PAT1, Topoisomerase II-associated protein PAT1. Members of this family are necessary for accurate chromosome transmission during cell division.	4.59108e-06

>NZ_CP036292.1|WP_145121984.1|4309410_4310406_-|SMP-30/gluconolactonase/LRE-family-protein
MTFALRSLALAAILFGLAAQPSSAQDSLGRIERLDPALDKLLAKDAKIEVLASGFTWSEGPLWVPEEDGYVLLSDIPRNSIFRWDAKRGVSLFMSPSGYTGNTYYGLEPGANGLALDAKGQVMMCEHGDRRVSVLTRDGGKRTLVDNYQGKRLNSPNDLVLHSSGAIYFTDPPYGMPKRYDDPRRELDFCGVYRLATDGTLTLISKELARPNGIGLSPDEKTLYVAQSDPKQAIWARFALNDDGTAGAMSILYDATDQVGKLPGLPDGLAIDPQGNLWASGPGGIYVFEPSGKLIGRLLTGQRTSNCTLGGPDGKDLFITADSYLCRVRLR
>NZ_CP036292.1|WP_145121983.1|4305969_4309389_-|acyltransferase-domain-containing-protein
MTDTNASSDRLKPYVIAAESQPQLVANLRALAGGESATSDSHAPERLLIVADGEEALRLLATRAADRLERRPGKPIHDVGGIYYYPEPLGLSGGIAWLFPGEGAQYLGMLQGLDSQWPEVESVLQQCDGFARQIGPPFHSLRYFIDGWQQDDRDRAEQLLRRLDNAMLSVLSAGWCLSEVAKMLGVPMQAAAGHSAGELAALMTAGSMELTTELPMFANVMNQMEVQSGGGDAELLAVAAAADKVQPVVFQALATAGMSDQAMVAMDNCPHQSIVVGRREATRRVRETIEKAGWIVEALSLQQPYHTPMFAPLMDPLRAAFDRVGFRSPDVPLYSCATGERFPDDSDQIRQLSLAHWHNPVRFQSLIQQMYADGVRLFLEVGPRGNISSFVADILRGQPHAAIPMDTPRLSTADQIVHAAAQLAAHHVPIELEALDPQFRQAQGNSFVQPSPRAEVAAAIAPGSDSVMSSHLETMQQLLAEQSDVMQQFLVAKNAGRTIGPRGGRRATAGNRSRRRLAAAAALPTDDILADESLWSGDEHAFEAAASGDGGLPRPELPLLGEVSEFEPGMHLVMHRLLDPAIEHYATHHTVGGREVSAIRPEQCGLPVMPMTFTLEMMMEAALQLAPELVVCSISRVQLSRWLAFYERDPITIRIEATLMPTDDDATTRVLVRVMDTGNREEPFGDKPKLAAVGTVTLAAAYPEAPLGQPLELTDAQQCETTLKTMYNNLFHGELFQGVRSLAKIGKQGIESTIEVLPRDELFRDDRPVEFLGDPVLLDVAMHPNAAWHLEQPDQTGRIMLPFVVKSVEFFGPRPAVGTRFECHGSLDEQSPRHFTHSVVSIDSEGRVWNRINGVRLWRFYLPFHEVNFHGPKNVYHLSEEFATQASAADDAIATARFAWLDDLSQPTLLRAAAEVLLSEQEYEDFIDAQIPHAEKVRWVFGRVVAKDAVRRLWHEQHGQRLYMSDIDTRHDGNGRPYALPRRAQHPSAGDVPAADAVMPNISVAHCNKISYAIASTARRVGVAVHPIAEVEEAQLAEALLPEEVSLLSACENRERCFAAILATKKAVAKATGLGLLGDWKNVRVTACDGEGQATAEIAGNLLAQLPAMAGHRWTAELSHDVDGKGDGKILAAVIDPTV
>NZ_CP036292.1|WP_145124184.1|4304382_4305780_+|RtcB-family-protein
MKTRELNNLGIPKGIAMQAAVEAVRNASAKGLKRPELRTAIAAIVEDPASAKDDPLWGSLADALQTVFSAQDRYIGRDEPAPWRQWGDGLEAGAVSQMVDACKLPVTVSGALMPDAHLGYGLPIGGVLATKDCVIPYAVGVDIACRMKMTVLDMPVETLDTNQDRLRNAIERETQFGIGASFRKRRQHEVMDADWRVSPITFQNKDKAWKQLGTSGSGNHFVEFGVLTLPAGDLGLAAGTYLALLSHSGSRGTGASICAHYSSVAKATHPELPRELQNLAWLNLDTQEGQEYWNAMNLMGEYAAANHACIHREIASHLGVEVLLDVENHHNFAWRESHGGEDLIVHRKGATPAGQGVLGIIPGSMGTPGYVVRGKGVEESLLSAAHGAGRRMSRTAAKKQFRWKEVKKFLNDRGVTLMSAGLDEVPMAYKDIDQVMASQHDLVETVARFDPRLVKMAEAGERPED
>NZ_CP036292.1|WP_145121981.1|4303334_4304351_+|RNA-3'-terminal-phosphate-cyclase
MIEIDGSRGEGGGQILRTSLALSMVTGQSVRFENIRAARSRPGLLRQHLTAVKAAAAVSGAKVDGDRLGSITLTFEPSKIQAGDYHFAIGSAGSCLLVLQTILPALMIADGPSRVDLEGGTHNPFAPPFEFLELSFLPLLKKIGPEVRLTLDRPGFYPAGGGRCSAAITPAEKLQPIELIQRGKLLNREALAIVSRLPAKIAARELETAARTLGWPKSTLKVEQVTTSPGPGNALLLSVSYENVTEVVTGFGDVKVSAERVAKRAAGELKKYLNGTAPVGVHLADQLLLPLAMAGGGQFRCQQTTQHTLTNIETIKMFLDLEIDVQPQEDESVLIRVG
>NZ_CP036292.1|WP_145121979.1|4302043_4302922_-|pyruvate-kinase
MDIRQPVQRTLVLAVLFAALGTTQHAVGVEAVSRDFNIQPLERIPAGTVITPDGAKGWSDLLLFVNGSLGKGDVDAASSTVKHYASLFNIAYMANVAKDAEGKFTLDKIGVGFTTKIDGQDVVITSDTHKSLGADLGMIGGAVFSANERALSEIVQVARYRDGAIFDAPTIMLRDGKHKKVIVRFFVWVSPQGSIGTVCWVLDGYGGSRYVVPNKEIVLLRPQLVENRVMHVDGDRFTLGIPSEDAFAVVSLPPGREYKIDDDLATLIAKKRYDAQSFFDTVQKLSQSLAAN
>NZ_CP036292.1|WP_145121978.1|4300245_4301538_+|Gfo/Idh/MocA-family-oxidoreductase
MQAARPTRRTALKTSVAFGGYLIAPEVSAADSTSANEQLNIACIGIGGRGAANVNGVKSQNLVALCDVDQQRAGKVFEQHNQAEKFADYRKMFDKLEKQIDAVVVSTPDHTHFHPSMAAMERGKHLYCEKPMAHSVGEVRQMTKMAVKQDVATQLGCQRHALANMHRSVELIQAGAIGDVSEVYSWVGGSRGMPSIPKTFPKVPETVDWDLWLGPAMPRPYDSTYCPYGWRFWWDFGTGETGNWGCHILDIPFWALGLKYPSRVEGSGPEVDDQRTPKQMATKMHFAEQGVDLHWDHASAGPAKLKELGIDGKGMNTLFIGSKGMLLTGFNKLRLLPEEKFADFKAPEPTIPKSPGFYKEWISACKGGEPATCDFRYSGPLAETVLLGNAAYRAGGGFDWDGPSLTASGNGAVQPFLKSEYRKGWEVAEV
>NZ_CP036292.1|WP_145121976.1|4298250_4299981_+|hypothetical-protein
MSTQNKPALAIVVLTAVQCLAIAAPAQAGPLCDWLFGRNRTAYYVPTGTYMPTPQGPTVTAGYLPTTNVAYPPVYNGQQQFGSTATAFPPQGMAVTSYSLPTANQPALPVGAPNYSAGYRGGSLNQYALPPSNTTTAYSPITGPNAGNQSAPLQSAPYYWPNQPRQSFFGSWWPNVGSYFGTGNYYPSNTPYPTNTYTSNYWSSYRVPTAGSAGAQMYPPTTAGYPTTGYPTAAPVTAGYPSYPTNPVVSGSPVVTTPSYSAGFSPHTSYSTNTYNVPVTYYRPIQSVDPRTGQQVTTMQGCQSYQTQVQRVPSYSLRGSAPASAPQCSGEPQCPPGSYESTPGYGSNQYAPAANPYNQQVTPPGTPTNRPSFGNAPAQPNYGTPPAAQPNYPAQGTPQGTYPQSTYPQGNNYGAPPQNGNDQTPMQQPQLQTNNNTSLSLPSFPGTGASNSQPGFQYQQQQPSTRLDVKPIPAPAQYQFQYNTTDDRTARREPAPAERGSSNVAQATYKTIQWAVPKSNQRTSAVTVSTQRNELPRLTAPRNTPPQQTAPRYNAPARPAPQGNGGYRDSGWVSGR
>NZ_CP036292.1|WP_145121974.1|4295834_4297856_-|helicase
MLDAASILGPDGRIAKRLTQYEHRPQQLGMADAVASAIEQGHHLVAEAGTGTGKSYAYLVPAILFATGDQREEETDDSAGDAPRPRRVVISTHTISLQEQLIMKDLPLLNSVIPREFSSVLVKGRSNYISLRRLKLAQTKAAGMFERDTQHVQLRQITEWAKETTDGSRSTVPTRIEAGVWDEVASDSGNCMGRKCETHDKCFYYAARRRMQNAQILVVNHALFFSDLALRQQDISLLPDYDAVILDECHTIEAVAGDHLGIRVSNGQIDYILNKLYNPRTQKGLLIAHDLQRLQQDVDRCHFAADEYFAGLLDWWDEDPRRNGRVRRPNLTPNVVSDPLSALAKQLKRYGDGMDNESVRKDFMSAHDRLTVLAESLKSWNDQLLDGYVYWVERTRSHRGFDRVNLAATPIDVGEALREMLFQKTRSVVMTSATLAVGSEANFDFYRSRVGLTGGESLRVGSPFNYRDQATLIVVDGLPDPSSQREAFERALPEQVKRYILETDGHAFVLFTSYGLLKKVAAAVTPWLIQQGMSLYTQGGDQSRTQILDAFRSNPRSVLFGTDSFWQGVDVPGDALQNVIITKLPFSVPDHPLLEARLEAIRAAGGNPFVDYQLPEAVIKLRQGFGRLIRTATDTGMVVILDPRVKTKPYGRIFLESLPDCHRVVHRVRARQS
>NZ_CP036292.1|WP_145121972.1|4294286_4295780_+|glycogen-synthase-GlgA
MNIVILTTEAVPFAKTGGLADVCGSLPQQLAQRGHKVTVIMPAFRQVFLAGQTIEPTEHNVSVAIAGKTVNARLLKSHLPGDQCEVLLIDQPSYYDREQLYGDAQGDFWDNCERFTFFCRAALSAIDTLDSPPDVVHCNDWQTGLIPAYIANRFESHPWMDHVATIMTIHNMAYQGQFWHWDMLLNGLGWDQFTPDKMEFYGHLNLLKTGLVFADSITTVSQRYAEEIQQPEFGCGLDGVLRNRHQVLSGIVNGVDYQIWDPATDEHLDAHYGIDDWKAGKRANRSALRQEMGLEDNPEIPLIGLIGRLADQKGWDLVTEMMNNWLGEGSPVQWVVLGTGDHRYHQTLSDLASRYSKRLAVHLGFSDRLAHRIEAASDMFLMPSRYEPCGLNQLYSLRYGTVPIVNPTGGLSDTVTDATEETVRLQTATGFHMSHYNARSLGETLDRAVTTYRENPGVWDQIVATGMQQDWSWQQSATRYEQIYLETIDRLHGAAVG
>NZ_CP036292.1|WP_145121970.1|4290720_4294011_-|hypothetical-protein
MSVSVNDFWNRITNSGLADAAQCRVWAVSYAQSKGAPPISAKDLAKWMIGAGELTLFQAKHLLSGSSQRLVFERYALTEPVDSPPLSRWFHAFDRDLGQAASKCLLFFLDPQQAAKTVGARFTQARRIQSDHLQAYDLIATPDGERVLWSHLPPGKTLAQRMQEGRLPADQVGRIGKNLAAALSALHAADLTHGSIHPEHIWVADHGDAILLRDPIVRPVSPLEQQPSGCLDSIGVESEGLPPSAMAAPEFSIPGKSPDKSTDLYALGCLLYLARFGEPPYSAAQPDALIQLHATATPAGLMPVKKGERSDPLLRVIAHLMAKNRDARIASADNLFSVFEVIESDPAAAAAVPAAAAAPQVAAAQPPQATPPPLPNAPQAVVAPQAAAETPTAKPAAAPPQPAAKSDAAPAAVPPKPQPAATKPAGDAPITTKKQTPAAAGPAKRDAAAAQAAQPAKPAAARPVEQPQPTAQPTATQPTSAQPVVPAQPAAAAAAPVQPTAAPVGTAVAAEPIANDPAVPKKKRPTGRTRKKKKKKKKAAAMVIGGVGFSMLTLLIAVLLMNNRGPRREPAADPVARGTAPAPTAVATTTPRAVTRPDDPTSSPGGTYLVSEDRFALWMPPDESQPPKLSMLPPGPQMIVVLRPANIIASGPGRKLMAALDTELQPALAALEKRIGVPLGEVERLTMAIEGGSAGGIQAALSVELVDEKSLGSLRKAWGDPEAAVVAGDQTIFAGEAVDTDAYYVAKESPVDSMSIQHFAVGSVKQIQQVAEIGGGEIPLPRQFEQTWNHVRGDGDLTVVATPNFLFADGKRMLIDYAPSVIAPLKQMLIPDSSVAMLTMQFAPTWYGEVRLAPGGGASAAALSQRLKQQFSDFPLQAEAFLNRSMPHPSWRGLALRLPRMLDALGAQSRTGVSENQAVANFYLPSHAAPNVLLGSWLAMNTPEGTVSMAAGPAATKPWTVEEMLEKPIKVSFEQEPLHFAGSTVVDEVNNIRPKGSPELKVVIIGNDLQKMGITQNQQIRNFKAEGVKVRDVLTQLVQRANIVKDLTDPADPQQALIWLVGPDPEAPDSKVVLITTRDGAKAAGYTLQPEFVIKQ
>NZ_CP036292.1|WP_145121986.1|4311215_4311668_-|IS200/IS605-family-transposase
MSTHQQLLYHIVFSVKDRRPLLQDDALRAQVWSYMAGIAKNLEGFAIKIGGFYDHAHVLVRIPAKVAVADFVGALKSNSSRQVNDARAGKLKFHWQDGYGAFTVSPSQVDRVVRYIENQLTHHAKQTFQDEYLALLAKHEIEFDPARVWE
>NZ_CP036292.1|WP_145121988.1|4312364_4314137_-|hypothetical-protein
MRCDSLPTLARCRFLPRLIGTFLLVVAGFAGASEAAQPLRPVDACFFDNDQTLLVVCQRSGEVLALDSTSGAVKTRLTVGGDLTAIERLPGGTAWAVDTAGDRLIEIDLEAGKLIAKSTIDCVRSPVSVIAGEANQLLVAGLWSRQVTCVARPAIDEPARPVWTQNLNFSPKTLRLLQPENVVLAVDAFGSQIAYLDASTGEQLRQIEFYGHRIRGMVDDPDGKRLIVSHQMLNSAAQSSNNDIHWGMMVSNDLRWLDRGRVMEADEENFYKDGHIDPIGIVGQGGADPNDLVCTVDGIVIVPLGGANEVAIGHEEFYELARLPVGINPVAVAVDSRGKTGWVVNRLDDSLTQIDIGERSVLKTVRLSEGWTPTTAELGERLFHNASLAHDGWMSCSSCHPGGHAVNERADNLSDGAYTSPKRVLSLLGRADTAPFGWIGADAKLEAQLQRTVRTTMQGHNKLTGEQVTQLTAFLESLVPPPPVVDASIPEVGESIARGQAIFQRQGCNDCHAGSKYTSAELYDVGLEDELGHTRFNPPSLLGVGQRGPRYFHDLRAESLEAVFTEHKHTLSKPLSQPDLEDLLTFLRSL
>NZ_CP036292.1|WP_145121990.1|4314332_4314788_-|hypothetical-protein
MTSYPNQSRSTVAKFFNAASLLALSLGLQLTLGCDDSDPRTGTVSGFVSLDDQPLGSGNILLLSESGASGGAELAADGTYTLSCTPGKYLVAVMPIAVEVGPDGKPTDPQAAANVVEIPMHYQDVGTSEIAIEVVAGDNDFDISLDSKSKR
>NZ_CP036292.1|WP_145121992.1|4314910_4315906_-|DUF1559-domain-containing-protein
MRRNSSRGFTLVELLVVIAIIGILVGLLLPAVQAAREAARRMQCSNNLKQIGLALHNYHDINRSLPIGSLGFLIQGWTVPVLPFVEQQTVYDQLAIGLPNGFDVNGVNAAVVDNWTPDMFWCPSSAATPMHLRVTSGNTVKMSTMSYIGIAGAPTSATNSSDPTGAGRCISGGQGYACANGTMIPNDTVRFRDLTDGLSNTVVIGESSSWGETAAGARIEIRTSAEWGAWAGSAASTTPPNNGTSYMWSANPYCRQITSLRYPIGTTLQLSGSGGNHRDGVNNALHSMHPGGVQVTRGDGGVGFLSETMEFLVLRNLCIRDDGNVIPGDVF
>NZ_CP036292.1|WP_145121994.1|4316172_4317621_-|DUF1501-domain-containing-protein
MNKLFNGHAPRRTFLADMGMGFTGLALGAMLQREARGHGAAWAPPTGEPHMPPKAKSVIWLFMNGGVSQMESFDPKPMLTKYAGKTISETPFAETQDPEKLALARVAAPDGNGNQRNKLYPLQKGFKKHGESGIEVSDWFPHIAKHVDKLAVVRSMYTTDSNHGAQTQFHSGRHLNDGNYPTLGAWVHYGLGSLNENLPQFISIGKREYWNKRDGHYLGPAHDAVPMRVDPDNPLDFSSPERPFARSSQEIGQDLIQRLNNRRQLEYPNDPAMAARIASYELAFRMQSSIPDVVDFSQETAQTQAMYGIDKPHSREFGMQLLGARRLVEQGVRFIQIQHGGGGAGAWDAHGKLEANHTKNSLAVDQPIGGLLEDLEQRGLLDETLVVFATEFGRTPGSQGSDGRDHHIYGFSVWMAGGGLKRGVVHGATDEIGFHAVEDRHYVTDVHATILKQLGLDSRKLEIPGRKRLEIDHGRPIDQIIA
>NZ_CP036292.1|WP_145121996.1|4317651_4320957_-|DUF1553-domain-containing-protein
MKLPSRICATIICLAVVAQASLFADDTQVDYETEVKPLLRERCYACHGALKQEGGLRLDTGAFMRQGGDSGAAVDLEEDPEFNLLVERTADTDPGSRMPPEFEGEPLSAEQVDLLKRWIAAGADSPADEVPEADPAQHWSFQPLARPDVPVVDDANWGRNPIDAWIAQGHQENELTPQSEASRVLLLRRLSFDLIGLPPSSEEIAAVVNDPSSDWYEKTVDRLLDDPRHGERWARHWMDNWRYSDWWGLNAQLRNSQRHMWHWRDWIVESLNNDVPYDEMVRLMLAADELAPDDPAKLRATGFLARNFYIFNRHTWMDQTVEHVGKGLLGLTMNCAKCHDHKFDPIGHDDYYKMRAFFEPYLVRLDNVPGELDVNKDGIPRVFDALVDAPTYRFIRGDEAQPDKSTVIAPGVPKMFEFEELTIEPVDLPPEAWQPARRPWVLDDHLAAAKKRQQASQTRVEKATAALEKARKSAEGSSPVEESTTPFTPIVEDFATLDDSRWKQGAGEWNHQPGRVEQTKDGQTRSVLQLMQNPPRDFDASIRFQIHGAGGWRTVGIGFDAPIAEDDSINESRQLVYASGHAGGPKVQASFLENGKSKYPGDGRSAADIQLDTDYTLRVQVRGNLINASLNDKPLIAFRTPLARVDGALQLITFDAIASISEFKLSALPGDVKLRDSSGATSVDPVVAAEFELAIAKAQAAVGKADLESVQARALAMRTAWDSNDDAAIREQAVAAIRAERAHAVAKARSTVTAEQVAVARATADKLKAAEKKLATAKEALAKAEASLKAEVKDSDQFTQLKGAKWTATRFQFTGRDDPDVEFPQQSTGRRAALARWITDPRNPLTARVAANHIWTRHLGQPLVASTFDFGRNGNAPTHPELLDWLASELIDSGWNMKHLHRLIVLSSTYRMDSSLSGMDDQLAKDPDNQHWWRRVPIRLESQAVRDAVLAVAGTLDDTMGGPSVLPADQDKSHRRSLYFFHSNNEKNLLLSTFDEASVAECYQREQSIVPQQALALSNSGLVLESSQQIASTIAADHPDDEAFVRQAFLLLLGIQPTAQEIDDCQSALTAWRELPEGSDDSARGNLIWAIINHNDFVTLR
>NZ_CP036292.1|WP_145121998.1|4320967_4321852_-|FCD-domain-containing-protein
MSITDFIRNDLALRLRSGRDLPAQLTLDSLAELYNVSFTPVRAAVADLIDEGLLRKGANRRLEACPLANALKEFDQLTEAPKPPADPSEKIADDLVLLSLEGKSVYLREEVTAEKYSLSRSAIRNILHQLAGEGMLDHIPRRGWRLRPFRQDDLQAFIEVREAMELKALQLARPRLDNQQLQAILERNASPTSAADRVPVDESLHEYLVATSGNAYIRDFFERQGRYFRLLFRWEDNDRSAALETLKQHRDVVQALLDEDWASAEAALSHHIRSNHPVLMTKPPTEAPPPTAPK
>NZ_CP036292.1|WP_145122000.1|4322009_4323188_+|galactonate-dehydratase
MKITAIETHVCHARMRNWIFVKVITDQPGLVGWGEATLEWHTRGVVGSIQDLSELLIGEDPTSIEHLWQMMWRQHFWHGSGVVRSTAISGIDLALWDILGKVHGVPCHRLWGGPVRDSIRMYCHLGGGNLESFYETPVDNARQFADLAQQAVDDGFSAFKSMAVPPTMPVEGLKAIKAADACVAAMREAVGDDIDIMVDCHARPSPAMGMQFAKALDQYGLYFFEEPCWPESLDSLAAINAAVTTPIATGERLTHLAAFRDLFAARGCEICQLDLTHCGGFTEARRIAALADAHRIALAPHNPQGPISTAASLEFGFSQPSYIICEAVHQDVPWRSDVVQESYVVDEATRTVTAGTAPGLGVTVDEDEIRKHPFQQELPQRVFYPDGAVGDW
>NZ_CP036292.1|WP_145122002.1|4323187_4324582_+|alkaline-ceramidase
MSDSTATVPAFHHAAFHGRVGIALNDITPPVGIYSRNWGAAAHDVADSIHRSLTLTATTIASLSGESPLVLIDADLGWWRTPELFPRFQQRLLEEFSLDSSQLIFALTHTHAGPPLLESTDPLPGMELTKPWLDSLLETAVTTVRQAFADASEATLEWQTGHCGLATTRDLPDPDSEGDRFLCGFDPEGQADGTLLLGRVTDAQGNLRATIVNYACHPTTLAWENTAISPDYIGAMRETIQKATGAPAVFLLGACGDQAPRYQYVGDTAVADGHGRELGYAALSTLAGMEPAGTQLAFEGAVTSGAPLAKWRHQPRKASEKIASVESSVDLPLKDWPSAAELEAQRIACTDRTLQERLLRRRDIRLRLGDGTTYPLPLYIWRMGDAVLVGSCCEAYSMLQRELRKRFPNNAIICMNLINGTIGYLPPADLYDKDVYAVWQTPFDRGCLEATLETLTQEIDDILR
>NZ_CP036292.1|WP_145122004.1|4324565_4325486_+|dihydrodipicolinate-synthase-family-protein
MTSSASETLLRGVLPVLQTPFTEQGEFDFETLDREIQWAFDTGADGIVVAMVSEILRLSEQGRRELAEHVCKAAQSRGTSVVSVGAESTPVAVELAQHAESVGASAVMAIPPISTGLSSAATRDYFAAIAASISIPLVVQDASGYVGSAIDIGVYSKLLEQFGADRILFKPEASPLGPNLSRLRDATAGKAQIFEGSGGINLVDCYRRGIVGTMPGTDLLDAIVALWNALQAGDDDRIYQLSLPISGIVALQLSAGLDGFLAIEKHLLVRRGIFKNTVQRQPVGWTLDAETAAEVDRLFDRLQDAI

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Crispr_ID: NZ_CP036292_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_18

4360363-4360441

Orphan

Consensus_repeat	Method
TTCCGCAACCGCAAGCTGGTTCGCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_18

>merge|NZ_CP036292|18|4360363-4360441|CRISPRCasFinder
CGTCGATGCCGCAAGCTGGTTCGCAACCGCAAGCTGGTTCGCAGCTGTAGACAGTTTCGCAACCGCAAGCTGGCTCGAT

>NZ_CP036292|18|18|4360363-4360441|CRISPRCasFinder
CGTCGATGCCGCAAGCTGGTTCGCA	ACCGCAAGCTGGTTCGCAGCTGTAGACAG
TTTCGCAACCGCAAGCTGGCTCGAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145122053.1\|4367736_4368195_+\|nucleoside-diphosphate-kinase	unknown	unknown	gnl\|CDD\|239876
NZ_CP036292.1\|WP_145122050.1\|4366031_4366835_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145122040.1\|4359174_4359735_-\|ribosome-recycling-factor	unknown	unknown	gnl\|CDD\|178850
NZ_CP036292.1\|WP_145122029.1\|4348751_4351535_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227713
NZ_CP036292.1\|WP_145122037.1\|4356167_4357442_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036292.1\|WP_145124186.1\|4369918_4370485_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122046.1\|4362525_4363860_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122055.1\|4368406_4369429_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145122057.1\|4370710_4371604_-\|phosphoribosylaminoimidazolesuccinocarboxamide-synthase	unknown	unknown	gnl\|CDD\|237571
NZ_CP036292.1\|WP_145122048.1\|4364498_4365731_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|99738
NZ_CP036292.1\|WP_145122031.1\|4351531_4353850_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|131281
NZ_CP036292.1\|WP_145122025.1\|4341047_4342823_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293765
NZ_CP036292.1\|WP_145122033.1\|4353750_4354656_-\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP036292.1\|WP_145122035.1\|4354672_4355683_-\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|223786
NZ_CP036292.1\|WP_145122052.1\|4367090_4367588_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122044.1\|4361109_4362462_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235977
NZ_CP036292.1\|WP_145097372.1\|4366815_4367085_+\|WXG100-family-type-VII-secretion-target	unknown	unknown	gnl\|CDD\|377587
NZ_CP036292.1\|WP_145122038.1\|4357601_4359155_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223553
NZ_CP036292.1\|WP_145122023.1\|4338517_4340362_-\|SLC13-family-permease	unknown	unknown	gnl\|CDD\|238535
NZ_CP036292.1\|WP_145122027.1\|4342864_4348726_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|173412

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145122053.1\|4367736_4368195_+\|nucleoside-diphosphate-kinase	gnl\|CDD\|239876	cd04413, NDPk_I, Nucleoside diphosphate kinase Group I (NDPk_I)-like: NDP kinase domains are present in a large family of structurally and functionally conserved proteins from bacteria to humans that generally catalyze the transfer of gamma-phosphates of a nucleoside triphosphate (NTP) donor onto a nucleoside diphosphate (NDP) acceptor through a phosphohistidine intermediate. The mammalian nm23/NDP kinase gene family can be divided into two distinct groups. The group I genes encode proteins that generally have highly homologous counterparts in other organisms and possess the classic enzymatic activity of a kinase. This group includes vertebrate NDP kinases A-D (Nm23- H1 to -H4), and its counterparts in bacteria, archea and other eukaryotes. NDP kinases exist in two different quaternary structures; all known eukaryotic enzymes are hexamers, while some bacterial enzymes are tetramers, as in Myxococcus. They possess the NDP kinase active site motif (NXXH[G/A]SD) and the nine residues that are most essential for catalysis.	7.39379e-77
NZ_CP036292.1\|WP_145122050.1\|4366031_4366835_+\|hypothetical-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.	4.76366e-06
NZ_CP036292.1\|WP_145122040.1\|4359174_4359735_-\|ribosome-recycling-factor	gnl\|CDD\|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	1.96431e-84
NZ_CP036292.1\|WP_145122029.1\|4348751_4351535_-\|hypothetical-protein	gnl\|CDD\|227713	COG5426, COG5426, Uncharacterized membrane protein [Function unknown].	2.2429e-05
NZ_CP036292.1\|WP_145122037.1\|4356167_4357442_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	1.58586e-23
NZ_CP036292.1\|WP_145122055.1\|4368406_4369429_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	6.88179e-59
NZ_CP036292.1\|WP_145122057.1\|4370710_4371604_-\|phosphoribosylaminoimidazolesuccinocarboxamide-synthase	gnl\|CDD\|237571	PRK13961, PRK13961, phosphoribosylaminoimidazole-succinocarboxamide synthase; Provisional.	8.8437e-165
NZ_CP036292.1\|WP_145122048.1\|4364498_4365731_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|99738	cd00614, CGS_like, CGS_like: Cystathionine gamma-synthase is a PLP dependent enzyme and catalyzes the committed step of methionine biosynthesis. This pathway is unique to microorganisms and plants, rendering the enzyme an attractive target for the development of antimicrobials and herbicides. This subgroup also includes cystathionine gamma-lyases (CGL), O-acetylhomoserine sulfhydrylases and O-acetylhomoserine thiol lyases. CGL's are very similar to CGS's. Members of this group are widely distributed among all three forms of life.	5.9256e-162
NZ_CP036292.1\|WP_145122031.1\|4351531_4353850_-\|VWA-domain-containing-protein	gnl\|CDD\|131281	TIGR02226, hypothetical_protein-transmembrane_prediction, N-terminal double-transmembrane domain. This model represents a prokaryotic N-terminal region of about 80 amino acids. The predicted membrane topology by TMHMM puts the N-terminus outside and spans the membrane twice, with a cytosolic region of about 25 amino acids between the two transmembrane regions. Member proteins tend to be between 600 and 1000 amino acids in length. [Hypothetical proteins, Domain].	6.91731e-22
NZ_CP036292.1\|WP_145122025.1\|4341047_4342823_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293765	cd16146, ARS_like, uncharacterized arylsulfatase. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036292.1\|WP_145122033.1\|4353750_4354656_-\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	7.33382e-31
NZ_CP036292.1\|WP_145122035.1\|4354672_4355683_-\|AAA-domain-containing-protein	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	3.36024e-99
NZ_CP036292.1\|WP_145122044.1\|4361109_4362462_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|235977	PRK07233, PRK07233, hypothetical protein; Provisional.	2.46305e-170
NZ_CP036292.1\|WP_145097372.1\|4366815_4367085_+\|WXG100-family-type-VII-secretion-target	gnl\|CDD\|377587	pfam06013, WXG100, Proteins of 100 residues with WXG. ESAT-6 is a small protein appears to be of fundamental importance in virulence and protective immunity in Mycobacterium tuberculosis. homologs have been detected in other Gram-positive bacterial species. It may represent a novel secretion system potentially driven by the pfam01580 domains in the YukA-like proteins.	3.57748e-05
NZ_CP036292.1\|WP_145122038.1\|4357601_4359155_-\|hypothetical-protein	gnl\|CDD\|223553	COG0477, ProP, Permeases of the major facilitator superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / Inorganic ion transport and metabolism / General function prediction only].	0.00118048
NZ_CP036292.1\|WP_145122023.1\|4338517_4340362_-\|SLC13-family-permease	gnl\|CDD\|238535	cd01115, SLC13_permease, Permease SLC13 (solute carrier 13). The sodium/dicarboxylate cotransporter NaDC-1 has been shown to translocate Krebs cycle intermediates such as succinate, citrate, and alpha-ketoglutarate across plasma membranes rabbit, human, and rat kidney. It is related to renal and intestinal Na+/sulfate cotransporters and a few putative bacterial permeases. The SLC13-type proteins belong to the ArsB/NhaD superfamily of permeases that translocate sodium and various anions across biological membranes in all three kingdoms of life. A typical ArsB/NhaD permease is composed of 8-13 transmembrane helices.	7.20445e-46
NZ_CP036292.1\|WP_145122027.1\|4342864_4348726_-\|hypothetical-protein	gnl\|CDD\|173412	PTZ00121, PTZ00121, MAEBL; Provisional.	3.4328e-24

>NZ_CP036292.1|WP_145122040.1|4359174_4359735_-|ribosome-recycling-factor
MSAEEIQLDAEERMEKAVAHLKHSLTGIRTGRATPGLVDSIRVEVYGSQTPLKQLASIGTPEPQQIVIRPYDQSTIKEIEKAIVAGDLGLNPQNDGHMIRLNVPPLSTEVRKKMVARIKELSEEAKVSIRNIRRDANKAADGEEKDKTMSEDDRDRVKNEIQDLTKKYESQIGEVAKARESEVMEG
>NZ_CP036292.1|WP_145122038.1|4357601_4359155_-|hypothetical-protein
MSDSPQVVNCPKCHAAVRAGQQMAGSRVRCPKCSSTFKVPGITATASDDDDWFNLGDPVADEPATAPPMDKPLSVPPAAAPVAPVVDDQPAAPPSAKTKAKSAVEPAAVDADDPLAKLAQSIPAADNASDDLFSSDDDSQDSDPFSLSLSEAPRRQNTSLDDWLGTEDVVPDAMPEVPETEFRFPCPVCESAHYAKPSQTGNRIKCGDCTSMITVPDPPKVVPKYSPSMESAATFELRDSVHRPDRQDSPFNKSAADLLRDAESTQMDEDLDKLYENPDVAGWFRDVFSVFTDPNVVMQLSIVAAVCSGGLIVWYLAQSAGAFVSAIVGAAALGVCGILLGSRYLSVMSRATADEEGEPRWPYEVSAGGLPSGLMVLVAALVASIPGQLAGSIIGEPLTLFWGVFVMISVWGLMPVVLLSMLENKTVFGVYSQNVIKSFERCMEPWGGMYFSSGLFFFAYFMLLAAPPSYGIVKSVIIGVGLVGLAFIQAGMLGRVVAAMVQLSTKQTTKKPQPNSH
>NZ_CP036292.1|WP_145122037.1|4356167_4357442_+|PQQ-binding-like-beta-propeller-repeat-protein
MKKIVLSIATLFAISSLVIAEDWPQWRGQARDGKSSETGLFSSWGEDGPPSVWTAEGLGEGYASVSVVDGTIYTTGNFEDGQAVVAIDANSGKRLWKQSVTKSEPKHSYEGSRSTPSVDGDRLYVVSSDGAIVCLDRADGSIRWQREFSDWKGKMMSSWGFSESPLVDGERVLCTPGGPQGLVVALNKMNGEEIWRSQLEASDDDSLKDGAGYSSIMISNGGGVKQYVQLVGRGLVGIRASDGKQLWRYARVGNTTANIPTPLIDGDQVFTSTAYGTGSALLKLKSDGAGGVDAEEIYWLEANQLQNKHGGMILIDGHIYCGTGNGNGLPICVEMKTGEIAWGPERGKGKGETSLVYADDHIVMRRDDGTVMLLRATPEKMDVLNSFKPAFQQGKSWSHPVISGGRLYLREQDKLMCFNLVKGA
>NZ_CP036292.1|WP_145122035.1|4354672_4355683_-|AAA-domain-containing-protein
MSETFSDPERAEQLVQACEKIRAQVGRVVVGQETVVEQILIAILARGHCLLEGVPGLAKTLMVKSLADAMHLAFHRIQFTPDLMPADITGTDIIQESDAGHRELVFDKGPIFTQMLLADEINRTPPKTQAALLEAMQEHEVTVGGTTYKLQEPFFVLATQNPIEQEGTYPLPEAQRDRFLFLVNVEYPTRDQEAMIIDRTTGSFDSKVEPVVTGDEIIAFQKTVRMVPLPEHVRNFVLDIVRSVRPREESCLPWVRQLVEWGPGPRACQQLVLASKARALLHGRYHVTIDDIEALALPVLRHRIVPTFNAEAEGISVADLVKRLLADVPRPKAQLL
>NZ_CP036292.1|WP_145122033.1|4353750_4354656_-|DUF58-domain-containing-protein
MTKLTDFLTPQDLAKTTNLQLLARQVMEGFCNGLHKSPHKGFSVEFKEHRQYVHGDEIRTIDWKLFGKTDRLYIREYEDETNLRCNILLDKSGSMGYCGSRAGGVSKHDYAVRLAACLGHLMLAQQDAVGLIHFDDAVRRIIPPRSKPTHLTAIVNELSGLKAERETELSSVFHQLVPKIPRRGLLVIISDLFGNIEELMKALAHFRHAKHEIVIFQIWDPDELDFPFKQWTQFQSLEQKSHRRLIDPAHLGKAYLKNLATFREALTAGCHRNRIDLVPVVTDRPYAEALASYLATRRRLR
>NZ_CP036292.1|WP_145122031.1|4351531_4353850_-|VWA-domain-containing-protein
MSPQPDRSGSRCHRPTVCRSVGIVSGHTEAAAMSFLNVALLGGLAAFAIPLIIHLLNRSKFKTLDWGAMHLLDSVVANNSRRVRLEQLLLLLIRCAIPALLAFCLARPVLTGWQSLPGDAPASTVILLDNSYSMDAIGASGTRIAEAVDDTRLIVDSSGKGSDTSVILTGGSPAPMFDTPVFDSKSITDQLPFLDSGRGATSLADSLELGASVVSAMANSRRNLILISDFQRSDVDALTPAAIERFRQQIDSQAVPPSITLIQRSGDAEQNIAIEDVQLSTRALGVGQQLKVRVRVKNYGVSDVPEARLQFIVDDRLVGVTELAVAGDATAQALFVHKFDAAGSHVLKFEVDAGDDLKTDNQYLAVVDVIDSIEVLMIDGDPSRKPMESETDFLAVALTPFSLGQMPLADLVETRIVKTDEVDQQTLEWARVVIMANVAKLDDERTAKLQDFVQRGGGLIVFTGNKVDVDWYNRVLHQQRGLFPLPIQGIGGGLDDGDRGARIVAQHFDHPALQIFNSGNSGSSELAQADIAQWYVLTKPASTSDNRIQAVSNKAKADASGTDPQASTLIRLDSGDPLWVEKPVGKGFVMACATTADADWNNLPLRPVFLPLVQQLVTSIATRGVPASNLTAGETLVALYDAAAADTTQVLSLPGNKQRSLRPVADQQRSVIRFAGTNQPGLYTLTQPDAPPRHFAVEIDRGESKLETIDAEQLQTLADALGADVVTDGAAFLALDSSRRHGREIWRLVLFALLGLLFVELFFQQRFSRVRQ
>NZ_CP036292.1|WP_145122029.1|4348751_4351535_-|hypothetical-protein
MTSLRFVGELPVWLGLFLAVAGAALAFGYYRRESFDLPGGLRWLLPCLRSVAIAMVIVSLTGPVLHHRQEIGELGNVRLLVDASQSMTTADPQMPLPRKLMIAHEQGWLPQGQFDTKLFDLAERISTTRRETLAALGTGAITPQAMQTALGNFTDAVTDLAPDVDAAIEAAAGLADENHVSPEPFEIEVLAKVKSLASEPIDDAEQASATRDRLIATVNGLQIYQQTFSDAFANYCQQWMQTQGDAALAGLQLFDQSLRIRRIEARLLDRDDGLIARLKDHHHVDVAALVGTREVPIWSSRGEVPIPESLDDVQSSMTTDLASGLIVESAQEASDPEGERSLGSATVLFSDGQHNAGPSPSQLAGVARSQQNAVYTVGFGTQSEPTDLALLQAEYPDTVYKSDRVRGTLVIKDRMPAERPFVVQISDGETVVWQQELKSMDVAQRRIDFDLAVEPLVDAAMDRFDNKVQRHSVPLELTAKIVPADGETELGNNSQAIRLAAVTQQHKVLLIDSRSRWEVRYLKNLFQRDSGWEIQTVILQSDDARQRLPRGEADGSFPNSKQALFEYDLIIYGDLPESVFNATEFSWLRDFVDQRGGGMIFIDGAHGELSRLTPESLGVLLPVTWSGDGDPKPAEGLQLTDSGRDNPALTLQGIGNENDQFWQQLPAPQRIALVEPTADAEVMAEAVVDGNRHPAIVGRSFGGGRVLYFAFDESWRWRYRVADQIHQRFWNQIARWVMPRPFAVSDQFLALDSGPLRYKAGDSASLRAKLRGPDGNLVADATVDALIWRDGRIVSTINLQPAENLPGDYRGETAALDPGEYEVTIRASGFNEAAFQAKTQFVVAPPQNKELEQIACNEALLIEMASAGGGEYLQEERLGEIVDLLRPLSSGRVVQSETLLWQSWPWFLCIVGLLSVEWWLRKRNGLL
>NZ_CP036292.1|WP_145122027.1|4342864_4348726_-|hypothetical-protein
MSNLSPETAAKLSEFGSRQKRLLIVRALCVGVVSLLVLMSLVAFVDWLWILSNKTRWSLSLAAYAIAALAVWWTSLRRWFTPQDPQSLAASFEVAEPELRENLLSAVELSQENAATNGSSQFRQLLQDKVASNIGRVDVRSLLPIRLIGRWLVGAIALTCLFGIVLSLPGLSFRQLITRAMVPGANLDRVSSTKVRVLQPSPASQIVPRGETIGIVVEISGPETNEVTLESYGESAGLTRQTMRAQGERRFAANITVRDPQVDYRILAGDAITRHYTLQSRPRPRVEGFQKTYHYPDYTQLADETITETHGDLIALEGTQVDLLLGTDQPISHAQILIETMGTDKLWTIDAVAREDGLLAATIPIRQAGVFKVLLESEETGFENTFSPKYEIRPEPDMIPRVGFLQQQETTLLRPANDIVPLMALAEDDLPLDTLRQMVSINGGRWTATPLQISPAAVVRKNWEMDLLSLNVKSGDTVSTMLVAIDRKGQRGESVPLKIVITSDDFDPNRHDALTVKAFVFDRLDQLARDLTASSDSADEIFKRNQATRRLTDADRVALIDIADKVEQQSGDAATVVRTLMPKIPAGMDAYDLEVTLRMLSEMQRELAGELKSFDAALGELEPDGKLKEDRYKHYHHRFKLAGETARWLQDRFSTIVSHDLMGGIAIDLDAIYQQQKLVADAGSQISEARLRRHQQVAINYVHALEDLMEEHAARIRSRSERTYVSLQELVARHREKLQLGLDNADDIQPLRRASEQFSKELHARLNQSMADGSLPEQLGRARLELVRRAGVLADPVDLAARHAGELVDARRKMLAAKDSAELAQTREVVDRAREAFDWRVRSLRDQIADRRTAQETRPDPLPIMQADLSLTQRAIDHVVAQLDGDPTDDAARQTLDDMRTIRDALRQLEVGHQLAALQPLAGKLLAQERWDSQAFVSRIEGPRLWDGIVKEVEVAAAIAKSADYPRETVNHINELRWGDPLNKAGERITMRRWRRESVSAAAGVEVLATRFQERLTEIAPIMADARKRIAALIPNIPQLADDLAEKTRQLEEQTKALAEEAKAEEAKAKEENKTPENADAAESEQDPEADAAELARQEKLAALQEQQQSLSEELQELLAALAEDASNQDLMEDEGRQRARDADDSIGMIQQPAETSAEELQAAAEAKSAQQQADALQKAADQQEQLADALEQVAEHFEKLDAGEDVAESREALRQAEMELPNARELEKEYARLERLNNIAEQAQSEQQRLLEQLERELQKSPEMQAALSDIAAEATAQALQALDYAKEQEDQARRSLEQSDPKVLSEKRKLQQDLQQVAREASAVADRMLSIAGNHAKKGDQPITAKKLTDAREQLKAAADAARSVTDNDLLNDMQDTVDDVNQKLQRAAEAVQQAATDSKQAAKEEVADQNQKDRMKRDAENDAKNLRNQMIQEFRREEQHANNYQKQTEQRIRNAENTLRTRQREADKAQQEAKKYPDNEWHQENAANTQQRAEQAQAVAEAEKQLNEDAKQRKQAASEKRQQMEKLDLGKFDAENPAAQMTQRVAEKAGSMLEQLADKMDAAAKRPTSDQQLAAPADALEATQRKQQSLGEDVRVASEDLARAARHEQRMKQSPATAAQLDQAAKQVGKVAEEQIAAAEKAAGSAAEKSRQQEDKPAGESPTPSAQAAEAVQQASDAIGEQAENVADMLAQSQAANAAAEQASAEPNSPSATSESGDSESGAATGEAASTPPSPAGTPPAGEDSASKSPAGEADAKPTGMQSEEPAAASSPAGSAGSPAEASSSGGKPAGQASPTAPRANESSVARGERLAEMLDDLDRAIAASSNRSEPSGESGQAASASSASMPSVAQMAANQAAAMSKRRSENQQQSDQPSPAGEDSMNAGEGAELEAMADGKLPAGAPERNGSDWGKLREKNAENATAGSRGEFASQYSDQIKAYFKVIAERSRK
>NZ_CP036292.1|WP_145122025.1|4341047_4342823_+|sulfatase-like-hydrolase/transferase
MTTLVVPTLAALFAQTVFMSSLRAQSNDRPNVLVILTDDQGWGDLSVNGNTNLSTPNIDSLARDGASFDRFYVCPVCSPTRAEFLTGRYHARSGVYSTSAGGERMNLDERTIAETFRDGGYATGAFGKWHNGMQYPYHPNGRGFDEYYGFCSGHWGDYFSPPLDHNGLIVQGDGFCIDDFTNKAIAFMESSVKQNKPFFTYVPFNTPHAPMQVPHPYWDRFKDKPLAMRHRDPQKEDVDFTRAALAMCENIDDNVGRMLAKLDQWQIADNTIVIYFCDNGPNSWRWNEGMKGRKGATDEGGVRSPLFIRWPKSIPAGKQVSQIAAAIDLLPTLAELTGQKVGGSKPLDGRSLAPLLTSDDADWPDRKIVSHWKNKVSVRNQRFRLDNRGELFEIATDPQQRVNVAEKFPEVMAELVAAAESYQTNVAAGYDDDQRPFPIGHADYRYTQVPARDANFNGGIQRSNRFPNCSYLKNWTQTDEVISWDATVGASGIYEVQLHYTCPAEDIGSTIELSFGESKLTCQLTEAHDPPLRGFENDRVKRPESYVKDFKVVTLGRIELTEGPGQLQLKALEIPGDQVMDFRLLFFTKIE
>NZ_CP036292.1|WP_145122023.1|4338517_4340362_-|SLC13-family-permease
MTTDIWIVTCILLATIIAFVLDRFRMDLVAFVSLLALLLTGILSPAEATAGFSNSLVLMIAGLFVVGGAILESGVADVAGRWLGRLGGTSTTRLTVAVMLASALLSAFLSSTGTVAVMLPVVLSLCRRAEVSPSKLLIPLAFAASLGGMLTLIGTPPNMVVNQELRGAGLETFQFFSFAPAGLLMLALGIVFMCTLGTRLLPAQATTAADVGRNQGLVSRPELIHSYGVDGQICEIRIPRGSNFAERTLRELGLRSTFHVNVLAVSTPDKIRSRVRSAIVRKCSPETLLHVGDTLFIKSANEEAISKLIREGLVEMVTTSASLPKVVHLAELIIPPRSKFVARTVRDLDFFRVYGAVVLALRKGNQPVSTRTSDTPLHPGDTLLVAANASALKRLGKSRNDVLLVSEQAEEGDAPLKPVAYWVIGILVGMLIAMSTGLSENVTAVLVAATLMVIAGAFRGTNAYQSINWQSIVLIASVMPLATALDKTGAFDLVVDAIVESPGLTSPWVLLLLLFVVTSILSQAISNTATSVLIAPLALELAAQLDVSPYPLLMGVALAASTAFSTPVASPINALVAGAGSYRFGDFLRVGVPLQLLILIATIAIVPLLFPFSP
>NZ_CP036292.1|WP_145122044.1|4361109_4362462_-|FAD-dependent-oxidoreductase
MSENDPGKSKWLVVGGGMAGLTLAHRLSQRGQEVSVCEAAPSFGGLTSACSLGDVVWDRFYHVTLLSDSHLRGLLKELDLEHEIRWVTTKTGFFSGGQLYSMSNSWEFLNFPPLTLIEKLRLGGTIFYTSKLRNWRRLEQIHVADFLKRLSGKGTFEKIWLPLLRAKLGETYQKASAAFIWSYISRMYKARRSGIKTEMFGYVPGGYARIIDRFVETLRGNGVRLLSSHGVQSITRCEAGGLDVDFGDGRIERFDNVISTIPSPIISQHCPELTEDEHQRLQGVEYIGVVCASMLLSESISPYYVTNITDDWVPLTAVIEMSTIVDRKELGGHALVYLPKYLPDSDPGLQESDAEIQERFLSTLEKMYSHFSRDQVQAFQISRAKHVMALPTIDYSQKLPPIVTSLPGFYALNGAHITKGNLNVNETIDLADEKLNDLVWPDFLSRCGSR
>NZ_CP036292.1|WP_145122046.1|4362525_4363860_-|hypothetical-protein
MNTREKFKSPTLHRLLVLLICLPAGVASAQPPENEAVPSAGQASPSEPAAPVDDEQPAAGSDTKAADKKGTVKEVTVLTAADRQRIDALIADLSSSKFAIREEAVAGLIEFGERAIPMLAAAADTPDPEVQLRIRILMSRLSNNDFESAVMAFLSGASDEMEGWDYARRLIGDSNAARELFVDASRQHRELMEELDKGPGLRMVAANKAADLVVRRMMLEFLPPERGDAVALLLTCGDRSAPIPPGVERVIVRIMNSPVTSETLKDAMLAPVYQKLVGFWMRRASVSYQPQAMYFALQHRVPESVELARDIVAEFVAAGEELTGPEIIDPKYGEGLEQALLVIAKYGDPSDVARLEPLRNDARRMPIGTDQPGDTHDRIEIQVRDIAVAVSIKILGGDLREAGYLNPREHAIVVFFTASLGFPGGGDELRSKPAKYLADLIAKP
>NZ_CP036292.1|WP_145122048.1|4364498_4365731_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MATDTVEQNSEKQTPAKQTPAKQGMSTKSVHAGEDRQKPGDAIADPIFCSSTFTFRTTDDVIDYCEGRSDREEYGRYGNPNERSVERKLAALDCGEAAIVYGSGMAAIVGLLMAKLNAGDEIVFFDQCYHRSREFCSKHLARFGVVTRQVPTGDYDAMEAAINENTRMLVSESPTNPHLTCIDLEQFVALGKAHEVETLIDATLATPYNIQPLEFGVDYVLHSATKYLGGHNDLLAGVIVGSAEALDPVRNLRGIMGAVNSPHNMYLLERGLKTFELRMQRHNANGQAIAEFLESHPRVERVYYPGLKSHPTHEIATQTMRGFGGLVTFTIKDADMRQTANIVDAAKIPRIAPSLGGVESLIEQPLVMSYYKCTPEQRASYGIADNMIRMSCGIENTEDLIADLDQALQA
>NZ_CP036292.1|WP_145122050.1|4366031_4366835_+|hypothetical-protein
MSADASGSPNLDTSVQRRQTLEHCIRDAPADVEPYLELAQIHRALDKPIEAQKVLEKAVRISGDHPEVLWQLEEAELARSLQRLKEFKELHNKHPTPDVTSDLERAQNEWAIRRAEVCRKRLQRDPSQTNLYIVMAEAMYEMGQFAEAAEALEPALNDPQECSKAHLVRGMCLQATNQPLEALASFRGAALRRAVQPAANIKLAALRHAADLASRLGLRATCKRYLRGILQLNPNDHVATQTLARLEAKGASDIHDLETTENVPSNR
>NZ_CP036292.1|WP_145097372.1|4366815_4367085_+|WXG100-family-type-VII-secretion-target
MSQAIVNPDHLRQFAGNLKVFTEELQQRAGSLSSQMNQLGESWRDQQHRRFAAEFEDELRQMARFVQSAEQHIPYLLRKADQIDAYLKG
>NZ_CP036292.1|WP_145122052.1|4367090_4367588_+|hypothetical-protein
MSSDVKSVDALRNLYAALLQLSDHCDDHVTQLRQLAHRFHEQITVQRRQYWQSQLQLAERRLQMAHEAMARAKISQDAADGTRNTEAEIMLARSKKRVAYCLDKLNVCKRISAEVDRVVDRFIGELGAMSELSESGLPQSANRLAGWIDALDLYTDNSGSPPPGP
>NZ_CP036292.1|WP_145122053.1|4367736_4368195_+|nucleoside-diphosphate-kinase
MERTLVLLKPDCVQRRLMGEIISRFEAKGLNIVGMKMMHVTPDLAKQHYAEHVEKPFYPSLESFITSAPIVALAIDGIEVIRVMRDLLGATNGCNAAPGTIRGDFSNSRQMNLVHASDGPEAAARELDLYFGTGDLCDFDHVTEEFMRAADE
>NZ_CP036292.1|WP_145122055.1|4368406_4369429_-|DUF1559-domain-containing-protein
MYSPLNGSRTLCRVTAPRPLRGFTLVELLVVIAIIGILVGLLLPAVQAAREAARRMQCSNNLKQMTLAMHNYESTHRVFPPGSLGYPFVWSPQSQLLPFVEQSNLKDLLVYEVPPMNAFGGGYNAAQVAQNDAAAQQRLPFITCPSDGEFVPGSDYGGISYPGSSGSGINNVGDASDDGSVSNADGIFFTKSKIGFRDVTDGTSHTIAFGEQLLGDGQNTAPANNDFRRRVVELAMATQTTTAACDPGSAPAWSGQRGAKWVNGHLADSMFNLFYTPNSKEPDCHNGYHNFGLVSARSNHPGGVQTSLVDGSVRFVGETVDLSVWRAAGTRSGGEIAGEL
>NZ_CP036292.1|WP_145124186.1|4369918_4370485_-|hypothetical-protein
MVLLIAVSCSIVGIPVVAPTAPKDGRFPCEHCACGCATAEYCWDKCCCHSDVEKLQWAAKNDVDPPRFLVERVAAQQRTTADQLAHSATPKKSCCCSGDRSVCSTGAAQPAEKADATGDEGSVALRVVRLEDAAKCRGVEMFWSVLSSVVVAWPKPLLESFDPPLLFTLCIQNDRAISVVSCPDPPAP
>NZ_CP036292.1|WP_145122057.1|4370710_4371604_-|phosphoribosylaminoimidazolesuccinocarboxamide-synthase
MTSNDPFEFDSNGALLRTHLPLPGQSGKVRDVYDLGDSLLIVSTDRISAFDWILPNGIPNKGSILTAMSRFWFDHLQVANHLISCEVPQQVIDLGIDASVLADRIMVVRKAQVVPFECVIRGFIEGSGWAEYQQSGAICGIDLPAGLRQCDRLPEPIFTPATKAETGHDENVSTEVMSAAIGAEQTELLRRLSLQVYTTAADHAAERGILIADTKFEWGLVDGEVILIDEVLTPDSSRFWPKSSYEPGHSQPSFDKQYVREWLSETDWDRNSPPPTLPADVVQRTGEKYREALDILT

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Crispr_ID: NZ_CP036292_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_17

4360210-4360289

Orphan

Consensus_repeat	Method
TTCCGCAACCGCAAGCTGGTTCGCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_17

>merge|NZ_CP036292|17|4360210-4360289|CRISPRCasFinder
TTCCGCAACCGCAAGCTGGTTCGCAACCGCAAGCTGGCTCGAAGCCACATGCTGGTTCGCAACCGCAAGCTGGTTCGCAG

>NZ_CP036292|17|17|4360210-4360289|CRISPRCasFinder
TTCCGCAACCGCAAGCTGGTTCGCA	ACCGCAAGCTGGCTCGAAGCCACATGCTG
GTTCGCAACCGCAAGCTGGTTCGCAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145122053.1\|4367736_4368195_+\|nucleoside-diphosphate-kinase	unknown	unknown	gnl\|CDD\|239876
NZ_CP036292.1\|WP_145122050.1\|4366031_4366835_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145122040.1\|4359174_4359735_-\|ribosome-recycling-factor	unknown	unknown	gnl\|CDD\|178850
NZ_CP036292.1\|WP_145122029.1\|4348751_4351535_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227713
NZ_CP036292.1\|WP_145122037.1\|4356167_4357442_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP036292.1\|WP_145124186.1\|4369918_4370485_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122046.1\|4362525_4363860_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122055.1\|4368406_4369429_-\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145122057.1\|4370710_4371604_-\|phosphoribosylaminoimidazolesuccinocarboxamide-synthase	unknown	unknown	gnl\|CDD\|237571
NZ_CP036292.1\|WP_145122048.1\|4364498_4365731_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|99738
NZ_CP036292.1\|WP_145122031.1\|4351531_4353850_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|131281
NZ_CP036292.1\|WP_145122025.1\|4341047_4342823_+\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293765
NZ_CP036292.1\|WP_145122033.1\|4353750_4354656_-\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP036292.1\|WP_145122035.1\|4354672_4355683_-\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|223786
NZ_CP036292.1\|WP_145122052.1\|4367090_4367588_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122044.1\|4361109_4362462_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235977
NZ_CP036292.1\|WP_145097372.1\|4366815_4367085_+\|WXG100-family-type-VII-secretion-target	unknown	unknown	gnl\|CDD\|377587
NZ_CP036292.1\|WP_145122038.1\|4357601_4359155_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223553
NZ_CP036292.1\|WP_145122023.1\|4338517_4340362_-\|SLC13-family-permease	unknown	unknown	gnl\|CDD\|238535
NZ_CP036292.1\|WP_145122027.1\|4342864_4348726_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|173412

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145122053.1\|4367736_4368195_+\|nucleoside-diphosphate-kinase	gnl\|CDD\|239876	cd04413, NDPk_I, Nucleoside diphosphate kinase Group I (NDPk_I)-like: NDP kinase domains are present in a large family of structurally and functionally conserved proteins from bacteria to humans that generally catalyze the transfer of gamma-phosphates of a nucleoside triphosphate (NTP) donor onto a nucleoside diphosphate (NDP) acceptor through a phosphohistidine intermediate. The mammalian nm23/NDP kinase gene family can be divided into two distinct groups. The group I genes encode proteins that generally have highly homologous counterparts in other organisms and possess the classic enzymatic activity of a kinase. This group includes vertebrate NDP kinases A-D (Nm23- H1 to -H4), and its counterparts in bacteria, archea and other eukaryotes. NDP kinases exist in two different quaternary structures; all known eukaryotic enzymes are hexamers, while some bacterial enzymes are tetramers, as in Myxococcus. They possess the NDP kinase active site motif (NXXH[G/A]SD) and the nine residues that are most essential for catalysis.	7.39379e-77
NZ_CP036292.1\|WP_145122050.1\|4366031_4366835_+\|hypothetical-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.	4.76366e-06
NZ_CP036292.1\|WP_145122040.1\|4359174_4359735_-\|ribosome-recycling-factor	gnl\|CDD\|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	1.96431e-84
NZ_CP036292.1\|WP_145122029.1\|4348751_4351535_-\|hypothetical-protein	gnl\|CDD\|227713	COG5426, COG5426, Uncharacterized membrane protein [Function unknown].	2.2429e-05
NZ_CP036292.1\|WP_145122037.1\|4356167_4357442_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	1.58586e-23
NZ_CP036292.1\|WP_145122055.1\|4368406_4369429_-\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	6.88179e-59
NZ_CP036292.1\|WP_145122057.1\|4370710_4371604_-\|phosphoribosylaminoimidazolesuccinocarboxamide-synthase	gnl\|CDD\|237571	PRK13961, PRK13961, phosphoribosylaminoimidazole-succinocarboxamide synthase; Provisional.	8.8437e-165
NZ_CP036292.1\|WP_145122048.1\|4364498_4365731_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|99738	cd00614, CGS_like, CGS_like: Cystathionine gamma-synthase is a PLP dependent enzyme and catalyzes the committed step of methionine biosynthesis. This pathway is unique to microorganisms and plants, rendering the enzyme an attractive target for the development of antimicrobials and herbicides. This subgroup also includes cystathionine gamma-lyases (CGL), O-acetylhomoserine sulfhydrylases and O-acetylhomoserine thiol lyases. CGL's are very similar to CGS's. Members of this group are widely distributed among all three forms of life.	5.9256e-162
NZ_CP036292.1\|WP_145122031.1\|4351531_4353850_-\|VWA-domain-containing-protein	gnl\|CDD\|131281	TIGR02226, hypothetical_protein-transmembrane_prediction, N-terminal double-transmembrane domain. This model represents a prokaryotic N-terminal region of about 80 amino acids. The predicted membrane topology by TMHMM puts the N-terminus outside and spans the membrane twice, with a cytosolic region of about 25 amino acids between the two transmembrane regions. Member proteins tend to be between 600 and 1000 amino acids in length. [Hypothetical proteins, Domain].	6.91731e-22
NZ_CP036292.1\|WP_145122025.1\|4341047_4342823_+\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293765	cd16146, ARS_like, uncharacterized arylsulfatase. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036292.1\|WP_145122033.1\|4353750_4354656_-\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	7.33382e-31
NZ_CP036292.1\|WP_145122035.1\|4354672_4355683_-\|AAA-domain-containing-protein	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	3.36024e-99
NZ_CP036292.1\|WP_145122044.1\|4361109_4362462_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|235977	PRK07233, PRK07233, hypothetical protein; Provisional.	2.46305e-170
NZ_CP036292.1\|WP_145097372.1\|4366815_4367085_+\|WXG100-family-type-VII-secretion-target	gnl\|CDD\|377587	pfam06013, WXG100, Proteins of 100 residues with WXG. ESAT-6 is a small protein appears to be of fundamental importance in virulence and protective immunity in Mycobacterium tuberculosis. homologs have been detected in other Gram-positive bacterial species. It may represent a novel secretion system potentially driven by the pfam01580 domains in the YukA-like proteins.	3.57748e-05
NZ_CP036292.1\|WP_145122038.1\|4357601_4359155_-\|hypothetical-protein	gnl\|CDD\|223553	COG0477, ProP, Permeases of the major facilitator superfamily [Carbohydrate transport and metabolism / Amino acid transport and metabolism / Inorganic ion transport and metabolism / General function prediction only].	0.00118048
NZ_CP036292.1\|WP_145122023.1\|4338517_4340362_-\|SLC13-family-permease	gnl\|CDD\|238535	cd01115, SLC13_permease, Permease SLC13 (solute carrier 13). The sodium/dicarboxylate cotransporter NaDC-1 has been shown to translocate Krebs cycle intermediates such as succinate, citrate, and alpha-ketoglutarate across plasma membranes rabbit, human, and rat kidney. It is related to renal and intestinal Na+/sulfate cotransporters and a few putative bacterial permeases. The SLC13-type proteins belong to the ArsB/NhaD superfamily of permeases that translocate sodium and various anions across biological membranes in all three kingdoms of life. A typical ArsB/NhaD permease is composed of 8-13 transmembrane helices.	7.20445e-46
NZ_CP036292.1\|WP_145122027.1\|4342864_4348726_-\|hypothetical-protein	gnl\|CDD\|173412	PTZ00121, PTZ00121, MAEBL; Provisional.	3.4328e-24

>NZ_CP036292.1|WP_145122040.1|4359174_4359735_-|ribosome-recycling-factor
MSAEEIQLDAEERMEKAVAHLKHSLTGIRTGRATPGLVDSIRVEVYGSQTPLKQLASIGTPEPQQIVIRPYDQSTIKEIEKAIVAGDLGLNPQNDGHMIRLNVPPLSTEVRKKMVARIKELSEEAKVSIRNIRRDANKAADGEEKDKTMSEDDRDRVKNEIQDLTKKYESQIGEVAKARESEVMEG
>NZ_CP036292.1|WP_145122038.1|4357601_4359155_-|hypothetical-protein
MSDSPQVVNCPKCHAAVRAGQQMAGSRVRCPKCSSTFKVPGITATASDDDDWFNLGDPVADEPATAPPMDKPLSVPPAAAPVAPVVDDQPAAPPSAKTKAKSAVEPAAVDADDPLAKLAQSIPAADNASDDLFSSDDDSQDSDPFSLSLSEAPRRQNTSLDDWLGTEDVVPDAMPEVPETEFRFPCPVCESAHYAKPSQTGNRIKCGDCTSMITVPDPPKVVPKYSPSMESAATFELRDSVHRPDRQDSPFNKSAADLLRDAESTQMDEDLDKLYENPDVAGWFRDVFSVFTDPNVVMQLSIVAAVCSGGLIVWYLAQSAGAFVSAIVGAAALGVCGILLGSRYLSVMSRATADEEGEPRWPYEVSAGGLPSGLMVLVAALVASIPGQLAGSIIGEPLTLFWGVFVMISVWGLMPVVLLSMLENKTVFGVYSQNVIKSFERCMEPWGGMYFSSGLFFFAYFMLLAAPPSYGIVKSVIIGVGLVGLAFIQAGMLGRVVAAMVQLSTKQTTKKPQPNSH
>NZ_CP036292.1|WP_145122037.1|4356167_4357442_+|PQQ-binding-like-beta-propeller-repeat-protein
MKKIVLSIATLFAISSLVIAEDWPQWRGQARDGKSSETGLFSSWGEDGPPSVWTAEGLGEGYASVSVVDGTIYTTGNFEDGQAVVAIDANSGKRLWKQSVTKSEPKHSYEGSRSTPSVDGDRLYVVSSDGAIVCLDRADGSIRWQREFSDWKGKMMSSWGFSESPLVDGERVLCTPGGPQGLVVALNKMNGEEIWRSQLEASDDDSLKDGAGYSSIMISNGGGVKQYVQLVGRGLVGIRASDGKQLWRYARVGNTTANIPTPLIDGDQVFTSTAYGTGSALLKLKSDGAGGVDAEEIYWLEANQLQNKHGGMILIDGHIYCGTGNGNGLPICVEMKTGEIAWGPERGKGKGETSLVYADDHIVMRRDDGTVMLLRATPEKMDVLNSFKPAFQQGKSWSHPVISGGRLYLREQDKLMCFNLVKGA
>NZ_CP036292.1|WP_145122035.1|4354672_4355683_-|AAA-domain-containing-protein
MSETFSDPERAEQLVQACEKIRAQVGRVVVGQETVVEQILIAILARGHCLLEGVPGLAKTLMVKSLADAMHLAFHRIQFTPDLMPADITGTDIIQESDAGHRELVFDKGPIFTQMLLADEINRTPPKTQAALLEAMQEHEVTVGGTTYKLQEPFFVLATQNPIEQEGTYPLPEAQRDRFLFLVNVEYPTRDQEAMIIDRTTGSFDSKVEPVVTGDEIIAFQKTVRMVPLPEHVRNFVLDIVRSVRPREESCLPWVRQLVEWGPGPRACQQLVLASKARALLHGRYHVTIDDIEALALPVLRHRIVPTFNAEAEGISVADLVKRLLADVPRPKAQLL
>NZ_CP036292.1|WP_145122033.1|4353750_4354656_-|DUF58-domain-containing-protein
MTKLTDFLTPQDLAKTTNLQLLARQVMEGFCNGLHKSPHKGFSVEFKEHRQYVHGDEIRTIDWKLFGKTDRLYIREYEDETNLRCNILLDKSGSMGYCGSRAGGVSKHDYAVRLAACLGHLMLAQQDAVGLIHFDDAVRRIIPPRSKPTHLTAIVNELSGLKAERETELSSVFHQLVPKIPRRGLLVIISDLFGNIEELMKALAHFRHAKHEIVIFQIWDPDELDFPFKQWTQFQSLEQKSHRRLIDPAHLGKAYLKNLATFREALTAGCHRNRIDLVPVVTDRPYAEALASYLATRRRLR
>NZ_CP036292.1|WP_145122031.1|4351531_4353850_-|VWA-domain-containing-protein
MSPQPDRSGSRCHRPTVCRSVGIVSGHTEAAAMSFLNVALLGGLAAFAIPLIIHLLNRSKFKTLDWGAMHLLDSVVANNSRRVRLEQLLLLLIRCAIPALLAFCLARPVLTGWQSLPGDAPASTVILLDNSYSMDAIGASGTRIAEAVDDTRLIVDSSGKGSDTSVILTGGSPAPMFDTPVFDSKSITDQLPFLDSGRGATSLADSLELGASVVSAMANSRRNLILISDFQRSDVDALTPAAIERFRQQIDSQAVPPSITLIQRSGDAEQNIAIEDVQLSTRALGVGQQLKVRVRVKNYGVSDVPEARLQFIVDDRLVGVTELAVAGDATAQALFVHKFDAAGSHVLKFEVDAGDDLKTDNQYLAVVDVIDSIEVLMIDGDPSRKPMESETDFLAVALTPFSLGQMPLADLVETRIVKTDEVDQQTLEWARVVIMANVAKLDDERTAKLQDFVQRGGGLIVFTGNKVDVDWYNRVLHQQRGLFPLPIQGIGGGLDDGDRGARIVAQHFDHPALQIFNSGNSGSSELAQADIAQWYVLTKPASTSDNRIQAVSNKAKADASGTDPQASTLIRLDSGDPLWVEKPVGKGFVMACATTADADWNNLPLRPVFLPLVQQLVTSIATRGVPASNLTAGETLVALYDAAAADTTQVLSLPGNKQRSLRPVADQQRSVIRFAGTNQPGLYTLTQPDAPPRHFAVEIDRGESKLETIDAEQLQTLADALGADVVTDGAAFLALDSSRRHGREIWRLVLFALLGLLFVELFFQQRFSRVRQ
>NZ_CP036292.1|WP_145122029.1|4348751_4351535_-|hypothetical-protein
MTSLRFVGELPVWLGLFLAVAGAALAFGYYRRESFDLPGGLRWLLPCLRSVAIAMVIVSLTGPVLHHRQEIGELGNVRLLVDASQSMTTADPQMPLPRKLMIAHEQGWLPQGQFDTKLFDLAERISTTRRETLAALGTGAITPQAMQTALGNFTDAVTDLAPDVDAAIEAAAGLADENHVSPEPFEIEVLAKVKSLASEPIDDAEQASATRDRLIATVNGLQIYQQTFSDAFANYCQQWMQTQGDAALAGLQLFDQSLRIRRIEARLLDRDDGLIARLKDHHHVDVAALVGTREVPIWSSRGEVPIPESLDDVQSSMTTDLASGLIVESAQEASDPEGERSLGSATVLFSDGQHNAGPSPSQLAGVARSQQNAVYTVGFGTQSEPTDLALLQAEYPDTVYKSDRVRGTLVIKDRMPAERPFVVQISDGETVVWQQELKSMDVAQRRIDFDLAVEPLVDAAMDRFDNKVQRHSVPLELTAKIVPADGETELGNNSQAIRLAAVTQQHKVLLIDSRSRWEVRYLKNLFQRDSGWEIQTVILQSDDARQRLPRGEADGSFPNSKQALFEYDLIIYGDLPESVFNATEFSWLRDFVDQRGGGMIFIDGAHGELSRLTPESLGVLLPVTWSGDGDPKPAEGLQLTDSGRDNPALTLQGIGNENDQFWQQLPAPQRIALVEPTADAEVMAEAVVDGNRHPAIVGRSFGGGRVLYFAFDESWRWRYRVADQIHQRFWNQIARWVMPRPFAVSDQFLALDSGPLRYKAGDSASLRAKLRGPDGNLVADATVDALIWRDGRIVSTINLQPAENLPGDYRGETAALDPGEYEVTIRASGFNEAAFQAKTQFVVAPPQNKELEQIACNEALLIEMASAGGGEYLQEERLGEIVDLLRPLSSGRVVQSETLLWQSWPWFLCIVGLLSVEWWLRKRNGLL
>NZ_CP036292.1|WP_145122027.1|4342864_4348726_-|hypothetical-protein
MSNLSPETAAKLSEFGSRQKRLLIVRALCVGVVSLLVLMSLVAFVDWLWILSNKTRWSLSLAAYAIAALAVWWTSLRRWFTPQDPQSLAASFEVAEPELRENLLSAVELSQENAATNGSSQFRQLLQDKVASNIGRVDVRSLLPIRLIGRWLVGAIALTCLFGIVLSLPGLSFRQLITRAMVPGANLDRVSSTKVRVLQPSPASQIVPRGETIGIVVEISGPETNEVTLESYGESAGLTRQTMRAQGERRFAANITVRDPQVDYRILAGDAITRHYTLQSRPRPRVEGFQKTYHYPDYTQLADETITETHGDLIALEGTQVDLLLGTDQPISHAQILIETMGTDKLWTIDAVAREDGLLAATIPIRQAGVFKVLLESEETGFENTFSPKYEIRPEPDMIPRVGFLQQQETTLLRPANDIVPLMALAEDDLPLDTLRQMVSINGGRWTATPLQISPAAVVRKNWEMDLLSLNVKSGDTVSTMLVAIDRKGQRGESVPLKIVITSDDFDPNRHDALTVKAFVFDRLDQLARDLTASSDSADEIFKRNQATRRLTDADRVALIDIADKVEQQSGDAATVVRTLMPKIPAGMDAYDLEVTLRMLSEMQRELAGELKSFDAALGELEPDGKLKEDRYKHYHHRFKLAGETARWLQDRFSTIVSHDLMGGIAIDLDAIYQQQKLVADAGSQISEARLRRHQQVAINYVHALEDLMEEHAARIRSRSERTYVSLQELVARHREKLQLGLDNADDIQPLRRASEQFSKELHARLNQSMADGSLPEQLGRARLELVRRAGVLADPVDLAARHAGELVDARRKMLAAKDSAELAQTREVVDRAREAFDWRVRSLRDQIADRRTAQETRPDPLPIMQADLSLTQRAIDHVVAQLDGDPTDDAARQTLDDMRTIRDALRQLEVGHQLAALQPLAGKLLAQERWDSQAFVSRIEGPRLWDGIVKEVEVAAAIAKSADYPRETVNHINELRWGDPLNKAGERITMRRWRRESVSAAAGVEVLATRFQERLTEIAPIMADARKRIAALIPNIPQLADDLAEKTRQLEEQTKALAEEAKAEEAKAKEENKTPENADAAESEQDPEADAAELARQEKLAALQEQQQSLSEELQELLAALAEDASNQDLMEDEGRQRARDADDSIGMIQQPAETSAEELQAAAEAKSAQQQADALQKAADQQEQLADALEQVAEHFEKLDAGEDVAESREALRQAEMELPNARELEKEYARLERLNNIAEQAQSEQQRLLEQLERELQKSPEMQAALSDIAAEATAQALQALDYAKEQEDQARRSLEQSDPKVLSEKRKLQQDLQQVAREASAVADRMLSIAGNHAKKGDQPITAKKLTDAREQLKAAADAARSVTDNDLLNDMQDTVDDVNQKLQRAAEAVQQAATDSKQAAKEEVADQNQKDRMKRDAENDAKNLRNQMIQEFRREEQHANNYQKQTEQRIRNAENTLRTRQREADKAQQEAKKYPDNEWHQENAANTQQRAEQAQAVAEAEKQLNEDAKQRKQAASEKRQQMEKLDLGKFDAENPAAQMTQRVAEKAGSMLEQLADKMDAAAKRPTSDQQLAAPADALEATQRKQQSLGEDVRVASEDLARAARHEQRMKQSPATAAQLDQAAKQVGKVAEEQIAAAEKAAGSAAEKSRQQEDKPAGESPTPSAQAAEAVQQASDAIGEQAENVADMLAQSQAANAAAEQASAEPNSPSATSESGDSESGAATGEAASTPPSPAGTPPAGEDSASKSPAGEADAKPTGMQSEEPAAASSPAGSAGSPAEASSSGGKPAGQASPTAPRANESSVARGERLAEMLDDLDRAIAASSNRSEPSGESGQAASASSASMPSVAQMAANQAAAMSKRRSENQQQSDQPSPAGEDSMNAGEGAELEAMADGKLPAGAPERNGSDWGKLREKNAENATAGSRGEFASQYSDQIKAYFKVIAERSRK
>NZ_CP036292.1|WP_145122025.1|4341047_4342823_+|sulfatase-like-hydrolase/transferase
MTTLVVPTLAALFAQTVFMSSLRAQSNDRPNVLVILTDDQGWGDLSVNGNTNLSTPNIDSLARDGASFDRFYVCPVCSPTRAEFLTGRYHARSGVYSTSAGGERMNLDERTIAETFRDGGYATGAFGKWHNGMQYPYHPNGRGFDEYYGFCSGHWGDYFSPPLDHNGLIVQGDGFCIDDFTNKAIAFMESSVKQNKPFFTYVPFNTPHAPMQVPHPYWDRFKDKPLAMRHRDPQKEDVDFTRAALAMCENIDDNVGRMLAKLDQWQIADNTIVIYFCDNGPNSWRWNEGMKGRKGATDEGGVRSPLFIRWPKSIPAGKQVSQIAAAIDLLPTLAELTGQKVGGSKPLDGRSLAPLLTSDDADWPDRKIVSHWKNKVSVRNQRFRLDNRGELFEIATDPQQRVNVAEKFPEVMAELVAAAESYQTNVAAGYDDDQRPFPIGHADYRYTQVPARDANFNGGIQRSNRFPNCSYLKNWTQTDEVISWDATVGASGIYEVQLHYTCPAEDIGSTIELSFGESKLTCQLTEAHDPPLRGFENDRVKRPESYVKDFKVVTLGRIELTEGPGQLQLKALEIPGDQVMDFRLLFFTKIE
>NZ_CP036292.1|WP_145122023.1|4338517_4340362_-|SLC13-family-permease
MTTDIWIVTCILLATIIAFVLDRFRMDLVAFVSLLALLLTGILSPAEATAGFSNSLVLMIAGLFVVGGAILESGVADVAGRWLGRLGGTSTTRLTVAVMLASALLSAFLSSTGTVAVMLPVVLSLCRRAEVSPSKLLIPLAFAASLGGMLTLIGTPPNMVVNQELRGAGLETFQFFSFAPAGLLMLALGIVFMCTLGTRLLPAQATTAADVGRNQGLVSRPELIHSYGVDGQICEIRIPRGSNFAERTLRELGLRSTFHVNVLAVSTPDKIRSRVRSAIVRKCSPETLLHVGDTLFIKSANEEAISKLIREGLVEMVTTSASLPKVVHLAELIIPPRSKFVARTVRDLDFFRVYGAVVLALRKGNQPVSTRTSDTPLHPGDTLLVAANASALKRLGKSRNDVLLVSEQAEEGDAPLKPVAYWVIGILVGMLIAMSTGLSENVTAVLVAATLMVIAGAFRGTNAYQSINWQSIVLIASVMPLATALDKTGAFDLVVDAIVESPGLTSPWVLLLLLFVVTSILSQAISNTATSVLIAPLALELAAQLDVSPYPLLMGVALAASTAFSTPVASPINALVAGAGSYRFGDFLRVGVPLQLLILIATIAIVPLLFPFSP
>NZ_CP036292.1|WP_145122044.1|4361109_4362462_-|FAD-dependent-oxidoreductase
MSENDPGKSKWLVVGGGMAGLTLAHRLSQRGQEVSVCEAAPSFGGLTSACSLGDVVWDRFYHVTLLSDSHLRGLLKELDLEHEIRWVTTKTGFFSGGQLYSMSNSWEFLNFPPLTLIEKLRLGGTIFYTSKLRNWRRLEQIHVADFLKRLSGKGTFEKIWLPLLRAKLGETYQKASAAFIWSYISRMYKARRSGIKTEMFGYVPGGYARIIDRFVETLRGNGVRLLSSHGVQSITRCEAGGLDVDFGDGRIERFDNVISTIPSPIISQHCPELTEDEHQRLQGVEYIGVVCASMLLSESISPYYVTNITDDWVPLTAVIEMSTIVDRKELGGHALVYLPKYLPDSDPGLQESDAEIQERFLSTLEKMYSHFSRDQVQAFQISRAKHVMALPTIDYSQKLPPIVTSLPGFYALNGAHITKGNLNVNETIDLADEKLNDLVWPDFLSRCGSR
>NZ_CP036292.1|WP_145122046.1|4362525_4363860_-|hypothetical-protein
MNTREKFKSPTLHRLLVLLICLPAGVASAQPPENEAVPSAGQASPSEPAAPVDDEQPAAGSDTKAADKKGTVKEVTVLTAADRQRIDALIADLSSSKFAIREEAVAGLIEFGERAIPMLAAAADTPDPEVQLRIRILMSRLSNNDFESAVMAFLSGASDEMEGWDYARRLIGDSNAARELFVDASRQHRELMEELDKGPGLRMVAANKAADLVVRRMMLEFLPPERGDAVALLLTCGDRSAPIPPGVERVIVRIMNSPVTSETLKDAMLAPVYQKLVGFWMRRASVSYQPQAMYFALQHRVPESVELARDIVAEFVAAGEELTGPEIIDPKYGEGLEQALLVIAKYGDPSDVARLEPLRNDARRMPIGTDQPGDTHDRIEIQVRDIAVAVSIKILGGDLREAGYLNPREHAIVVFFTASLGFPGGGDELRSKPAKYLADLIAKP
>NZ_CP036292.1|WP_145122048.1|4364498_4365731_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MATDTVEQNSEKQTPAKQTPAKQGMSTKSVHAGEDRQKPGDAIADPIFCSSTFTFRTTDDVIDYCEGRSDREEYGRYGNPNERSVERKLAALDCGEAAIVYGSGMAAIVGLLMAKLNAGDEIVFFDQCYHRSREFCSKHLARFGVVTRQVPTGDYDAMEAAINENTRMLVSESPTNPHLTCIDLEQFVALGKAHEVETLIDATLATPYNIQPLEFGVDYVLHSATKYLGGHNDLLAGVIVGSAEALDPVRNLRGIMGAVNSPHNMYLLERGLKTFELRMQRHNANGQAIAEFLESHPRVERVYYPGLKSHPTHEIATQTMRGFGGLVTFTIKDADMRQTANIVDAAKIPRIAPSLGGVESLIEQPLVMSYYKCTPEQRASYGIADNMIRMSCGIENTEDLIADLDQALQA
>NZ_CP036292.1|WP_145122050.1|4366031_4366835_+|hypothetical-protein
MSADASGSPNLDTSVQRRQTLEHCIRDAPADVEPYLELAQIHRALDKPIEAQKVLEKAVRISGDHPEVLWQLEEAELARSLQRLKEFKELHNKHPTPDVTSDLERAQNEWAIRRAEVCRKRLQRDPSQTNLYIVMAEAMYEMGQFAEAAEALEPALNDPQECSKAHLVRGMCLQATNQPLEALASFRGAALRRAVQPAANIKLAALRHAADLASRLGLRATCKRYLRGILQLNPNDHVATQTLARLEAKGASDIHDLETTENVPSNR
>NZ_CP036292.1|WP_145097372.1|4366815_4367085_+|WXG100-family-type-VII-secretion-target
MSQAIVNPDHLRQFAGNLKVFTEELQQRAGSLSSQMNQLGESWRDQQHRRFAAEFEDELRQMARFVQSAEQHIPYLLRKADQIDAYLKG
>NZ_CP036292.1|WP_145122052.1|4367090_4367588_+|hypothetical-protein
MSSDVKSVDALRNLYAALLQLSDHCDDHVTQLRQLAHRFHEQITVQRRQYWQSQLQLAERRLQMAHEAMARAKISQDAADGTRNTEAEIMLARSKKRVAYCLDKLNVCKRISAEVDRVVDRFIGELGAMSELSESGLPQSANRLAGWIDALDLYTDNSGSPPPGP
>NZ_CP036292.1|WP_145122053.1|4367736_4368195_+|nucleoside-diphosphate-kinase
MERTLVLLKPDCVQRRLMGEIISRFEAKGLNIVGMKMMHVTPDLAKQHYAEHVEKPFYPSLESFITSAPIVALAIDGIEVIRVMRDLLGATNGCNAAPGTIRGDFSNSRQMNLVHASDGPEAAARELDLYFGTGDLCDFDHVTEEFMRAADE
>NZ_CP036292.1|WP_145122055.1|4368406_4369429_-|DUF1559-domain-containing-protein
MYSPLNGSRTLCRVTAPRPLRGFTLVELLVVIAIIGILVGLLLPAVQAAREAARRMQCSNNLKQMTLAMHNYESTHRVFPPGSLGYPFVWSPQSQLLPFVEQSNLKDLLVYEVPPMNAFGGGYNAAQVAQNDAAAQQRLPFITCPSDGEFVPGSDYGGISYPGSSGSGINNVGDASDDGSVSNADGIFFTKSKIGFRDVTDGTSHTIAFGEQLLGDGQNTAPANNDFRRRVVELAMATQTTTAACDPGSAPAWSGQRGAKWVNGHLADSMFNLFYTPNSKEPDCHNGYHNFGLVSARSNHPGGVQTSLVDGSVRFVGETVDLSVWRAAGTRSGGEIAGEL
>NZ_CP036292.1|WP_145124186.1|4369918_4370485_-|hypothetical-protein
MVLLIAVSCSIVGIPVVAPTAPKDGRFPCEHCACGCATAEYCWDKCCCHSDVEKLQWAAKNDVDPPRFLVERVAAQQRTTADQLAHSATPKKSCCCSGDRSVCSTGAAQPAEKADATGDEGSVALRVVRLEDAAKCRGVEMFWSVLSSVVVAWPKPLLESFDPPLLFTLCIQNDRAISVVSCPDPPAP
>NZ_CP036292.1|WP_145122057.1|4370710_4371604_-|phosphoribosylaminoimidazolesuccinocarboxamide-synthase
MTSNDPFEFDSNGALLRTHLPLPGQSGKVRDVYDLGDSLLIVSTDRISAFDWILPNGIPNKGSILTAMSRFWFDHLQVANHLISCEVPQQVIDLGIDASVLADRIMVVRKAQVVPFECVIRGFIEGSGWAEYQQSGAICGIDLPAGLRQCDRLPEPIFTPATKAETGHDENVSTEVMSAAIGAEQTELLRRLSLQVYTTAADHAAERGILIADTKFEWGLVDGEVILIDEVLTPDSSRFWPKSSYEPGHSQPSFDKQYVREWLSETDWDRNSPPPTLPADVVQRTGEKYREALDILT

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Crispr_ID: NZ_CP036292_19

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_19

4670447-4670562

Orphan

Consensus_repeat	Method
CGCGGGGCGTTGCCCACGCGGTTAAACGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_19

>merge|NZ_CP036292|19|4670447-4670562|CRISPRCasFinder
CGCGGGGCGTTGCCCACGCGGTTAAACGAGAGCGTGCCCTACGGGGTACGGTTGGGGGGGGACGCGATGGATGGCGCGGGGGAAGCACGCGGGGCGTTGCCCTCGCGGTTAAACGA

>NZ_CP036292|19|19|4670447-4670562|CRISPRCasFinder
CGCGGGGCGTTGCCCACGCGGTTAAACGA	GAGCGTGCCCTACGGGGTACGGTTGGGGGGGGACGCGATGGATGGCGCGGGGGAAGCA
CGCGGGGCGTTGCCCTCGCGGTTAAACGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145122333.1\|4672468_4673203_-\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|223881
NZ_CP036292.1\|WP_145122337.1\|4678413_4678704_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145124211.1\|4664322_4665249_+\|carboxylating-nicotinate-nucleotide-diphosphorylase	unknown	unknown	gnl\|CDD\|238806
NZ_CP036292.1\|WP_145122336.1\|4675032_4676514_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237057
NZ_CP036292.1\|WP_145122326.1\|4659948_4663497_+\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|274225
NZ_CP036292.1\|WP_145122327.1\|4665233_4668878_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|372622
NZ_CP036292.1\|WP_145122322.1\|4655360_4656470_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|240291
NZ_CP036292.1\|WP_145122325.1\|4658399_4659803_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122331.1\|4671572_4672043_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376792
NZ_CP036292.1\|WP_145122338.1\|4678759_4681072_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224455
NZ_CP036292.1\|WP_145122323.1\|4656384_4657677_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237862
NZ_CP036292.1\|WP_145122328.1\|4668874_4670155_-\|DNA-repair-exonuclease	unknown	unknown	gnl\|CDD\|277319
NZ_CP036292.1\|WP_145103146.1\|4663906_4664227_-\|helix-hairpin-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378965
NZ_CP036292.1\|WP_145124210.1\|4653775_4654501_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237855
NZ_CP036292.1\|WP_145124212.1\|4676521_4678003_-\|IMP-dehydrogenase	unknown	unknown	gnl\|CDD\|376340
NZ_CP036292.1\|WP_145122332.1\|4672042_4672462_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP036292.1\|WP_145122330.1\|4671036_4671318_-\|DUF1778-domain-containing-protein	unknown	unknown	gnl\|CDD\|370057
NZ_CP036292.1\|WP_145122335.1\|4674386_4674764_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122334.1\|4673610_4674285_+\|HEAT-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145122324.1\|4657721_4658312_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145122333.1\|4672468_4673203_-\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|223881	COG0811, TolQ, Biopolymer transport proteins [Intracellular trafficking and secretion].	4.7389e-26
NZ_CP036292.1\|WP_145124211.1\|4664322_4665249_+\|carboxylating-nicotinate-nucleotide-diphosphorylase	gnl\|CDD\|238806	cd01572, QPRTase, Quinolinate phosphoribosyl transferase (QAPRTase or QPRTase), also called nicotinate-nucleotide pyrophosphorylase, is involved in the de novo synthesis of NAD in both prokaryotes and eukaryotes. It catalyses the reaction of quinolinic acid (QA) with 5-phosphoribosyl-1-pyrophosphate (PRPP) in the presence of Mg2+ to produce nicotinic acid mononucleotide (NAMN), pyrophosphate and carbon dioxide. QPRTase functions as a homodimer with two active sites, each formed by the C-terminal region of one subunit and the N-terminal region of the other.	2.11524e-121
NZ_CP036292.1\|WP_145122336.1\|4675032_4676514_-\|hypothetical-protein	gnl\|CDD\|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	0.000320034
NZ_CP036292.1\|WP_145122327.1\|4665233_4668878_-\|AAA-family-ATPase	gnl\|CDD\|372622	pfam13514, AAA_27, AAA domain. This domain is found in a number of double-strand DNA break proteins. This domain contains a P-loop motif.	1.94996e-77
NZ_CP036292.1\|WP_145122322.1\|4655360_4656470_-\|hypothetical-protein	gnl\|CDD\|240291	PTZ00146, PTZ00146, fibrillarin; Provisional.	8.061e-05
NZ_CP036292.1\|WP_145122326.1\|4659948_4663497_+\|c-type-cytochrome	gnl\|CDD\|274225	TIGR02604, Piru_Ver_Nterm, putative membrane-bound dehydrogenase domain. All proteins that score above the trusted cutoff score of 45 to this model are large proteins of either Pirellula sp. 1 or Verrucomicrobium spinosum. These proteins all contain, in addition to this domain, several hundred residues of highly variable sequence, and then a well-conserved C-terminal domain (TIGR02603) that features a putative cytochrome c-type heme binding motif CXXCH. The membrane-bound L-sorbosone dehydrogenase from Acetobacter liquefaciens (Gluconacetobacter liquefaciens) (SP\|Q44091) is homologous to this domain but lacks additional sequence regions shared by members of this family and belongs to a different clade of the larger family of homologs. It and its closely related homologs are excluded from the this model by scoring between the trusted (45) and noise (18) cutoffs.	1.07985e-48
NZ_CP036292.1\|WP_145122331.1\|4671572_4672043_-\|hypothetical-protein	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	1.19923e-19
NZ_CP036292.1\|WP_145122338.1\|4678759_4681072_-\|hypothetical-protein	gnl\|CDD\|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	4.53679e-16
NZ_CP036292.1\|WP_145122323.1\|4656384_4657677_-\|hypothetical-protein	gnl\|CDD\|237862	PRK14948, PRK14948, DNA polymerase III subunit gamma/tau.	0.00165792
NZ_CP036292.1\|WP_145122328.1\|4668874_4670155_-\|DNA-repair-exonuclease	gnl\|CDD\|277319	cd00840, MPP_Mre11_N, Mre11 nuclease, N-terminal metallophosphatase domain. Mre11 (also known as SbcD in Escherichia coli) is a subunit of the MRX protein complex. This complex includes: Mre11, Rad50, and Xrs2/Nbs1, and plays a vital role in several nuclear processes including DNA double-strand break repair, telomere length maintenance, cell cycle checkpoint control, and meiotic recombination, in eukaryotes. During double-strand break repair, the MRX complex is required to hold the two ends of a broken chromosome together. In vitro studies show that Mre11 has 3'-5' exonuclease activity on dsDNA templates and endonuclease activity on dsDNA and ssDNA templates. In addition to the N-terminal phosphatase domain, the eukaryotic MRE11 members of this family have a C-terminal DNA binding domain (not included in this alignment model). MRE11-like proteins are found in prokaryotes and archaea was well as in eukaryotes. Mre11 belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	2.5407e-44
NZ_CP036292.1\|WP_145103146.1\|4663906_4664227_-\|helix-hairpin-helix-domain-containing-protein	gnl\|CDD\|378965	pfam12836, HHH_3, Helix-hairpin-helix motif. The HhH domain is a short DNA-binding domain.	5.17249e-23
NZ_CP036292.1\|WP_145124210.1\|4653775_4654501_-\|hypothetical-protein	gnl\|CDD\|237855	PRK14900, valS, valyl-tRNA synthetase; Provisional.	1.53554e-13
NZ_CP036292.1\|WP_145124212.1\|4676521_4678003_-\|IMP-dehydrogenase	gnl\|CDD\|376340	pfam00478, IMPDH, IMP dehydrogenase / GMP reductase domain. This family is involved in biosynthesis of guanosine nucleotide. Members of this family contain a TIM barrel structure. In the inosine monophosphate dehydrogenases 2 CBS domains pfam00571 are inserted in the TIM barrel. This family is a member of the common phosphate binding site TIM barrel family.	0
NZ_CP036292.1\|WP_145122332.1\|4672042_4672462_-\|biopolymer-transporter-ExbD	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	1.45924e-22
NZ_CP036292.1\|WP_145122330.1\|4671036_4671318_-\|DUF1778-domain-containing-protein	gnl\|CDD\|370057	pfam08681, DUF1778, Protein of unknown function (DUF1778). This is a family of uncharacterized proteins. The structure of one of the hypothetical proteins in this family has been solved and it forms a helix structure which may form interactions with DNA.	1.5548e-14
NZ_CP036292.1\|WP_145122334.1\|4673610_4674285_+\|HEAT-repeat-domain-containing-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.	1.57452e-08
NZ_CP036292.1\|WP_145122324.1\|4657721_4658312_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	7.23965e-29

>NZ_CP036292.1|WP_145122328.1|4668874_4670155_-|DNA-repair-exonuclease
MVRFIHAADIHLDSPMLQLEHYEGAPADEIRRSTRRALTNLIDLAIEKQVDFVLIAGDLYDGDWPDHNTGLFFTSEVARLRAAEIPLYFISGNHDAANKLTKALPLPTNPDGSPVQLSSTKVDSVILEDLGVAIHGRGFRKQAETDNLSEKYPRATRDLLNIGMLHTSLQGAQGHAPYAPCTPQQLADKEYDYWALGHIHIREDRAIEGSCPIVFSGNTQGRSVRETGAKGCVLVELDPIAPPKLEFQPLDVCRWEICEIDATEIDRIDDLIQQCKTRMQAICANNPDRTSIVRVRVVGQTPLYSTLQARLEHWQSVMRQETFDIDEGSIWMERLRVKATAPREAITYDASGPIGELLQTIGSVSADPDAMAAIQSALEPLVAKLPIELVEDGDGVAWNHQDQIRQWLDEAEPLLLNRLATLEADV
>NZ_CP036292.1|WP_145122327.1|4665233_4668878_-|AAA-family-ATPase
MRFASLDLIAYGHFQNQRIDLSGGQYGLHVIYGPNEAGKSTTLRAITSLLYGFDNVTSDNFRHQNRDLRVGARIIDHDGEEIRCVRRKGRTGTLYCGDDDNAIDEAVLQKMLRGVDKAAFGDRFGITHQSLVEGGEMMVKGDGDVGQSLFAAGAGLGQLKQIQDAIEDECGKLFKKSGSKSELNRLLGELREKKRQLKESLLPVKTFVNLQQQREEKQVESENYRNAVRETRTEVKRLETLRDAIPLRAEWIQLTEQLAPLADVPMLSPDFSTRQHQASTTWAASQQKMQLVRARIEDQQKKLSALGAPDPLLDQAETIDSLVQAVGGISKAAIERPGLVKRRDMTQAQIVSKLRGIGRNDSDDVWNLQLPHDLRSKIKQLAKQYVALTQRADASAEDLESLQLQVQQVDAAIAAIEQPPSADALAAALQQAGDAATLVGDHEAAQAALARESRAVATQLRKLTGLECDGQTATALPVPQRETIEKCAGEWEAISSRQQQLVEKQAAYTDKLDQLTTRLHELHGAGEVPSEQELIAAREQRDQLSASLAATDSAADINCDRQAFESLMAMIEQCDQMSDRLRREAERVSRRATLEAERGSIERAQQRLAEDSEQLQSQRQQFADRWNAIWADCGLQPKSPREMLGWLTEHQRLVELYEAQVEAEQAVARHASRIERVTQQLLAAMPNGSASPASDDLVALVRQAGAAVATTRKQQQEYEERTKQKQQLQQSLPQSQRRNEQIQEELAQWQAQWREVTSRLELDEQAGTDEVDGVVEAYHELVVDQKEFDSFQRRIDGIDTDARAFDAQVRGLGLPIKDASLDASKIVEGWAKDLKQAQKTQTQREQIEQQIAQDQRDLTALEQERIDCQTQLNLLCKEACCDAPEQLAEVYRNSQQKQQLEHRRQEHYSRLTQMAGTLPVDEFLEKVAAVDPETLDQDIDELHDKLVGLEEDHTASCQELGQLDQQRKAMDGGASAADLQQEIHELLSRIDRHAAQYARLRVAETLLNRAVTNYRDRNQAPILKIASDYFRRLTLDSYSELRADNNDKGDPVLLGVRAATGQSVDLRGMSQGTADQLYLALRLASLKHSFASSDPIPLVVDDILIQCDLQRSRAAFELLAELSNDTQVIFFTHNEALLETARECVDANQLFVQTLTRDSVEPTAEVKSPTKAEPKRKSTTKAKSKAKPKPESKPKPEPVDEPDDVEDDLFQLKS
>NZ_CP036292.1|WP_145124211.1|4664322_4665249_+|carboxylating-nicotinate-nucleotide-diphosphorylase
MAVEYQQIRVDAPLEDDFRQLIRLAVREDFDRQIDWTTVSLVPEDRIGKCQVAVREAGIAAGLVTLPWIIDEMNLELRIETLVEDGDRVAAGQIVAQIEGSARDILSSERIVLNTLCRMFGIATFTDRFVQQISGTKARLYDTRKTTLGWRRMDKYAVRCGGGTNHRLGLFDAFLIKDNHLALAGPGEAIPPSEAVAKAKSWAGGESAGMKAPQIVEVEVDTLEQFQDVLPAGPDIILLDNFSLDDLRQAVAIRNEKSPQIELEASGNVKLETIREIAETGVDRISSGALTHAARWLDLGLDWTHDFS
>NZ_CP036292.1|WP_145103146.1|4663906_4664227_-|helix-hairpin-helix-domain-containing-protein
MMLRSLPLQIGLLAVLGVLFIISLRTPTEYPIDPQPPPIHLPVWIDPNTADAMELSMMPSIGPQTADRIIADREANGPYRSLSDLDRVPGIGPKTLQRLAPFIHIK
>NZ_CP036292.1|WP_145122326.1|4659948_4663497_+|c-type-cytochrome
MIRTLPTLVCIFCCCASSFGQPSPPPADQQRERFRLPPGFEIQLVVSDPEIGQPMNLNFDARGRLWVTHSVEYPYPAAGEGVQPDRGKFAGGGDHPPRDRLSIVEIGPTGNASQVTHFVDGLNIPIGQTPLKDGSEGLVYGIPSIFHVVDRDGDGRSDTQTALYSRFGNIDVHGNANAFTRWIDGWIYGCHGFSNHSEITDAAGRTVVMDSGNTYRFRSDGSHFQQFTWGQVNPFGITFDAWGNIFDSDCHSKPVYQLLRGATYPHFGNPEPAIGFGPSMIDHAHGSTGICGPAYYSADHFPEEFRDNLFICNPVTGRVHRDKLRRVGSTLLCDTQPDFITTDDPWFRPVDAIVGPDGALYIADFCNLVIGHYEAPLDDPDRDRTHGRIWRVVWNGAPSAPPQSVDLTKLSTADLIVRLSDPNLQVRTLATNYLIDSRANEVLDPLCATLASESDPFPRAHGLWILERLDAMDSEAIERFANDSDPLVRVHLLKMLAERENLLESERQFVVQGLRDPDGFVRRAAADALGQHPTFANIAPLLNAWDAAPAEDSHLIHVLRLSLQRHLETGDLPHAPGTASFSIQQLTAEQQRRLLEIASVSGGDRAAEIVFELADPREIDPAILVRSAILITRTASVASQLRLVKLAPQWFATDPGQQLSLLSAIFDGATQRGGESAELKRQLRQWLQRLAPAELQTLQAGGSDWSRQPVPGQEASESPWGIRHRGSADGNTDAKFWDSISHGEHLTGVLRSPSFPLPETLSFWLCGHNGHPKKKSSDANHIRLVLVDSGKTITQQLPPRNDTAQRYTWTIDPDRIGQQAAIEIVDADQGNAYSWIAAGRFEPPVVQVADEPQELRLIELIGSLNLSQFADTIDLLISDRRQSLDVRQQAIRTSIRLGRTERLFAIVSDLLSDPSQPTALRMQAAAALAGFDTDASRDRLVAAIAQSPASLQREIASGLARTTVGIDRLFDAIAAGNASARLLQEPAIIDALHRNANEKQRQQIDELTQGLPPANEKLAEILAHHRALAHRSSTAGSAAAGRIVFDKNCAACHRIGSSGQLVGPQLDGVGNRGVERLLEDILDPNRNVDVAFRSLTVVTIDGTVVNGLLRRHEGETIVLADSTGREITISTDDIETQQKSTVSVMPGNFSESLAEQEIQNLLAFLIEQRVEDESPAGPAASP
>NZ_CP036292.1|WP_145122325.1|4658399_4659803_+|hypothetical-protein
MADAKTALQPSTIAGIAPADPLDLLFMNAASEQPQFDPYHQWLGIPPDQQPANLYRLLGLERFESDADVIDVAANRQIAYLRQVGVGAKRDPAKRLVAELADARRVLLSPPLRKAYDRQLVASSAPQTDDVENPSSDRPPAESETIRHGPSLRIPTRPPQKHSRRKRQRKFALGGTAILTVLVVVGGGYLATRGPTTIATPATKTVTAKVDPAAPRRHIVHKPIIAGVPQPPRHVASDPKTRSLTDVFDQKFRSAQQATPAATSSPDKQTDSLPILVDFEGDAWRAALAIDDLALFNQHHSVRDGKLFVLQAEDESYIGTPLRLKNVKLTADQSLAVDARIPKGLKHNSGVALQAGDFTLALRVDSRSTLLAGTVRSGVSIELASIPYESDPQGLQQPYRLRITCPPADSTTYSWRIDVPSGEAVEGTFAAEQTMTGGEAIVQAWRYDARNSHFWIDNLASDTLDAP
>NZ_CP036292.1|WP_145122324.1|4657721_4658312_-|sigma-70-family-RNA-polymerase-sigma-factor
MSNEQMDLGLTTNELACPKWMVMNEASSNGKPLSHATLEQAVSELLPYWLRMAQRLSGDPEIAEEAVQDALVRVAKSWKGFRGQATLQTWVGRIVIHCVRDRMTARKQPTGCQEAAPDVVAKSRGPVEELLASEQQQRVRTAIGLLPDRQREVLTLTIWEAKSVAEVGELLEISTQNVYATLHVARQRLKEILREE
>NZ_CP036292.1|WP_145122323.1|4656384_4657677_-|hypothetical-protein
MSDQNSKPNRDLLDTELDALLRAADPARQPIPVERVRQQWDMLAAGRRRRIRRLRYGGLATAACLLLAFGIGWQLEFGRDLKNSRHANVPQDPVAVPTQPTVTNQTPTTPPQRPERPETTTEPTEMLAEAEQQSPAEPTDVPAAKEASLVEQFEQAIAALSSNDLREGYRVVEQLRRLPRPQQRELLLAVPEMQNQATRRQAMALITAAAGNDATAVHTAWLSFDSTRDDSWQAMVDRSDASQWSALIPLAKSDQQKRVLCRKLVADWQAAGLDRIVELASAAAWRSAVQIEAAALDPQASKRLLKIIDADSQPMRVAGGFVLAAMKRPEVDRVLIQLIVQGRSQMAAYQGLIIRNTTEARQFLAHASVQFELSPAFAAARRRWMTWGPQAFQWVSETRSRNDVQDGILQDDPLYQLRVVGVPGRGPIRG
>NZ_CP036292.1|WP_145122322.1|4655360_4656470_-|hypothetical-protein
MFKTAFFKTILCTSFVLLASPAGAQSADDTQPIIRVYDVRDLTDPQTSLLGDWLTGENQAKVSGLSHGVLGGGGSGGAGFGGGSGGAGMEGGDAGGGGFFSIPSHIQPQFGGGGMGGMGGGMIGAAANPMFELMNLLTQFRVGDAQLSHLGHLLVAKATQRGHQELEAVLQTLRENSLSTPTIEVALRLVAIESAESGEFHRMETADIEALAKRKDAISATVRCGNGRIGTIASGARRSFVISAVPVVGANGSNSSSGRSVGYSPRVITPMIGLVGKVRPILDRGASGDSRSAQIDIGIAYSIGSDEILSATFGNGTTIDRIDLTAMEYESQVNVVEDRWTLAGMSTATDGSGEQQGHMAVVVQWREVR
>NZ_CP036292.1|WP_145124210.1|4653775_4654501_-|hypothetical-protein
MDHEGCRGWWVRIQRGDQHVSKLFSDGVYGSTRKAEIAATKFRDEQLKELPARVFKGSKGPRLNAAGYYLRTRVRRGKDEQAWVAIWTEDGRQLEKSFSINQHGNAAAKKLAKAYRQEMVEKLIGGGGETKATKKAPVKKKAAVKKTTTKKAAAKKSVKKAPVKKTAKKKAAVKKTAVKKSPVKKATKKAAVKKKAAVKKAAVKKKAPVKKTATKKAPVKKVAKKAAVKKKVAKKKATKRR
>NZ_CP036292.1|WP_145122330.1|4671036_4671318_-|DUF1778-domain-containing-protein
MAKSLKTDRIEARVEPSVRKLIVAAAQLEGRSVSEFLVASAKERAEAALYRQTVIRLTAEDQLRFAEAILDPPPLNDAMHEALALHEQLIDPS
>NZ_CP036292.1|WP_145122331.1|4671572_4672043_-|hypothetical-protein
MRLPSGHGREPLELKMTPMIDVVFLLLVFFLWTSSFEEPEFLMPSAIADPPLAAGAEATLQPPPASEPFDEIIVRIQWTSGAATLLFNDQPLPSLDALRQRLQAILDVGVLPPVIVDPDPEVPMGDAIRVYDTARSLGFDRVFFAARADTAPPSSN
>NZ_CP036292.1|WP_145122332.1|4672042_4672462_-|biopolymer-transporter-ExbD
MRTPSRTGRSDGSANMTPMIDVVFLLIIFFLVSSHLARQESRIPLDLPVADASVDQPPLNDVFTINVLPDGAWQVSGTEVDRAMLDRLLQSHHGEHGPDAAVRIRTDRSVAYGQVEPLLRAASGAGLWNASFAVYQETR
>NZ_CP036292.1|WP_145122333.1|4672468_4673203_-|MotA/TolQ/ExbB-proton-channel-family-protein
MLNSSLAMAGLLAQTVDADAGGGSFWQILFSGGIVGLLIILLLFSLSLIAAFLIFDQFMALRRAEVIPEGVVEPIQKLLAERRVKEADAICRQKPSLLTFVMMSGLAEVDFGWPSVEKAMEEALAEQSARMMRRIEYLSVIGNIAPMVGLLGTVTGMIFAFQRVAISQGGAGAGDLAEGIYQALVTTVGGLIVAIPALGAFAVLRNRVDGLVAEVAYLAQHAMSGLKRRSVKRPVPGTPIPPVQ
>NZ_CP036292.1|WP_145122334.1|4673610_4674285_+|HEAT-repeat-domain-containing-protein
MSQPATRTSRIVNQYRRYLDASDSLDFFRTVNESYTVDTLLTLLRRGDSESRRASALALSMVGDVRATEALGHRLSDRDRGVRLIADDAFRAILVRDAAPSHHQNLLQVMHLNDGGEFAAALTPAMILVQQAPRYAEAHHQLAIAYLGLQEYASADCAFRNCLWHCRFHYLAWSGLADCRRAIGDQREALKHLHRAIAICPDFESARIQARAIRRSLNRNPPTH
>NZ_CP036292.1|WP_145122335.1|4674386_4674764_-|hypothetical-protein
MKPPIYFLFVESRCVATLADPRVEEMFWCSFRIEPVDQWGDAIVHDPKTWETVGLVIKDHDGNVTNPHVFSGGFDDFCDRKTDRLAFRSLFPTAASKRSCLRRKLLSAFAKLFGSSPAGPRITEY
>NZ_CP036292.1|WP_145122336.1|4675032_4676514_-|hypothetical-protein
MSLAAAMPLAALETLPAQAQVTWDTPRAAQTQAAPRTTTASRFDASFSNATSDTSVVARRPSQPQPASSQPNKLQWRSSDRVAPRTFASGSKTNLSADNGPVMRVAYQQEGAVPDDLFGEQPGSNRQAPGSDADPFDNDVFGNPFQAPPAATPAPVSPPAGGNAPDALRMPELSQPNEAAPELPPAVAPAPQPEQPSPLLPPTNDQRDNLDESKLDMLDNNPFKRGPAGETDSPSDRQEDSQPTEPESEPDFVPRRGFGITPPQPRTNLSCEDLRQEVASRTISRISLDISPAYRPDVLDDKKFAELRSDFEKNQKPRDWRGVDGSLLGRGTLYDLSYQDVVLHTESGGTQKIDISRLSEADLAFLSKEWGLPRVCRIAQVAYQPRNWVPSTMTWKASNLCHNPLYFEEVQLERYGHSAGPLKQPLISTAHFFVNIAVLPYKMGIHAPDECQYALGYYRPGNCAPYMLPPIPLSLRGTLSQAAVVAGGFWLIP
>NZ_CP036292.1|WP_145124212.1|4676521_4678003_-|IMP-dehydrogenase
MSQEKLIQEGFTFDDVLLTPQYSAVVPSEVDTSTHLTSNIRLQIPLISSPMDTVTESEMAIALAKVGGLGVIHKNLSIEAQTEEVLKVKRSANGIIFDPVTLHPDEKVSRAQELMDQKNVSGIPIVYADGKLAGILTRRDLRFLESPDRLISEVMTHENLVTAVGNVTLEEAERILTEKRVEKLLLVDEERILTGLITIKDIDMMQRFPSASKDGQGRLRVGAAIGVHDYERAESLINQGVDILTVDSAHGHSKNVIETVKKLKQQWQIDLIAGNVATADGARDLIDAGVDAIKVGIGPGSICTTRVISGVGVPQVTAIMEAARVANERNIPIIADGGIRFSGDITKAIAAGAKVVMIGSLFAGLTESPGKMILYQGRTFKAYRGMGSIGAMAQGSSERYRQSATESGKLVPEGVEGRVPFKGPLSEYVFQLVGGLRAGMGYIGTQTIEELRTRARFIKVSAATVRENHPHDIAITQEAPNYSPEVHHSGDSN
>NZ_CP036292.1|WP_145122337.1|4678413_4678704_+|hypothetical-protein
MQFLPLIIQLVTGAVGGNLTGSLFKKLDLGLIGNSIAGILGGGLGGQLLGMLGIAAAPGGSLDIGTVLGSIASGGVGGGVLMVIVGLIKSVLLKGK
>NZ_CP036292.1|WP_145122338.1|4678759_4681072_-|hypothetical-protein
MQRYRSLLSAIAIAIGISGELCAQRIDRSTQPIASEGSESIQQSTAQPSELWSPKGLSTRSRQLEYRPENDVVTVAQNASPASADRPDVKKVDPSLFRDPAIEPVKNLPTDYPPVRHRIYPDSSPCPKPENPDDDTAVIVLVQREPDRVASRNIKPEPTPEPLPERLFPEPRVASLHTFQAPTASPVQPAPTATQVSMAPRSQLHPPVVAPQNTEPQLPAELLPPLRSVSPQGQQAAVPLPPGNPEAAPAATDELLLVPIDTPWWEALVARPLRPDTSPLSVTLEQLIVGALNHSNQIKVFSKLPLIRATTVGEADAAFDWNSFLSNRWDDISDPVGSTLTVGGNATRFNDHNLSGAAGLRRQTHSGAQVEMSQRLGWQDNNSNFFVPAPQGTSQLTLRMSQPLMRGRGTVYNNSITVLAQIDRRQADDEFQRQLQGHLLEVMRSYWELYLERGVLLQKLQSYQRAAEIARQLELRAQLDASESQLVSAQATLAQRRSDLFRAQSAVVNAESKIRALVNDPALDTSDACELIPAEPPSIETYLVDMELQRALAVQNRPEISQAIKQIKSASVRLNMSKHELLPVLNLVTEAYVSGLQGDGDVAASLARQFDTGAGSYGVGFEYELPVGNRGAKFRNRRRMLELSQLQYQYKSTLSTVQLEVEIAVRELQTSQREMTAKFEAQQARTRQLETLMQRWQRNMNDAVTGSFALENLLDAQERVAQAEFEYLQSQLTYNLSIGNLHRATGTLLQSEEVSQYRVSDFEPARGTAR

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Crispr_ID: NZ_CP036292_20

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_20

5209252-5209347

Orphan

Consensus_repeat	Method
TCAGGCCCAACGGGGCCGGCCGTA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_20

>merge|NZ_CP036292|20|5209252-5209347|CRISPRCasFinder
TCAGGCCCAACGGGGCCGGCCGTATGCCAGCCCAGGGCAACGCCCTGGGAAAACCGATGCCCACAAAACCGTTTCAGGCCCAACGGGCCGGCCGTA

>NZ_CP036292|20|20|5209252-5209347|CRISPRCasFinder
TCAGGCCCAACGGGGCCGGCCGTA	TGCCAGCCCAGGGCAACGCCCTGGGAAAACCGATGCCCACAAAACCGT
TTCAGGCCCAACGGGCCGGCCGTA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145122677.1\|5196296_5196575_-\|DUF1778-domain-containing-protein	unknown	unknown	gnl\|CDD\|370057
NZ_CP036292.1\|WP_145122682.1\|5209967_5211005_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|378117
NZ_CP036292.1\|WP_145122687.1\|5220811_5221951_-\|transglutaminase-domain-containing-protein	unknown	unknown	gnl\|CDD\|376628
NZ_CP036292.1\|WP_145122678.1\|5196831_5197311_-\|DUF1772-domain-containing-protein	unknown	unknown	gnl\|CDD\|227787
NZ_CP036292.1\|WP_145122688.1\|5222080_5222467_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145124240.1\|5200248_5201250_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122684.1\|5213792_5216807_-\|response-regulator	unknown	unknown	gnl\|CDD\|236848
NZ_CP036292.1\|WP_145124239.1\|5197752_5198205_+\|cytochrome-c-nitrite-reductase-small-subunit	unknown	unknown	gnl\|CDD\|274453
NZ_CP036292.1\|WP_145122683.1\|5211027_5213664_-\|malto-oligosyltrehalose-trehalohydrolase	unknown	unknown	gnl\|CDD\|200464
NZ_CP036292.1\|WP_145122676.1\|5195777_5196296_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379326
NZ_CP036292.1\|WP_145122680.1\|5201402_5201999_+\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|226648
NZ_CP036292.1\|WP_145122686.1\|5220341_5220755_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122675.1\|5193372_5195427_-\|exo-alpha-sialidase	unknown	unknown	gnl\|CDD\|271234
NZ_CP036292.1\|WP_145122689.1\|5222560_5223658_+\|alpha/beta-hydrolase	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122681.1\|5201995_5202196_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224662
NZ_CP036292.1\|WP_145122685.1\|5217297_5218932_+\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP036292.1\|WP_145124241.1\|5202335_5208236_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|380081
NZ_CP036292.1\|WP_145124242.1\|5218939_5220292_+\|response-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP036292.1\|WP_145122679.1\|5198322_5199894_+\|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552	unknown	unknown	gnl\|CDD\|349426
NZ_CP036292.1\|WP_145122690.1\|5223788_5224520_+\|phospholipase	unknown	unknown	gnl\|CDD\|224495

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145122682.1\|5209967_5211005_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|378117	pfam09084, NMT1, NMT1/THI5 like. This family contains the NMT1 and THI5 proteins. These proteins are proposed to be required for the biosynthesis of the pyrimidine moiety of thiamine. They are regulated by thiamine. The protein adopts a fold related to the periplasmic binding protein (PBP) family. Both pyridoxal-5'-phosphate (PLP) and an iron atom are bound to the protein suggesting numerous residues of the active site necessary for HMP-P biosynthesis. The yeast protein is a dimer and, although exceptionally using PLP as a substrate, has notable similarities with enzymes dependent on this molecule as a cofactor.	2.00607e-35
NZ_CP036292.1\|WP_145122687.1\|5220811_5221951_-\|transglutaminase-domain-containing-protein	gnl\|CDD\|376628	pfam01841, Transglut_core, Transglutaminase-like superfamily. This family includes animal transglutaminases and other bacterial proteins of unknown function. Sequence conservation in this superfamily primarily involves three motifs that centre around conserved cysteine, histidine, and aspartate residues that form the catalytic triad in the structurally characterized transglutaminase, the human blood clotting factor XIIIa'. On the basis of the experimentally demonstrated activity of the Methanobacterium phage pseudomurein endoisopeptidase, it is proposed that many, if not all, microbial homologs of the transglutaminases are proteases and that the eukaryotic transglutaminases have evolved from an ancestral protease.	1.28066e-14
NZ_CP036292.1\|WP_145122678.1\|5196831_5197311_-\|DUF1772-domain-containing-protein	gnl\|CDD\|227787	COG5500, COG5500, Predicted integral membrane protein [Function unknown].	4.85572e-41
NZ_CP036292.1\|WP_145122677.1\|5196296_5196575_-\|DUF1778-domain-containing-protein	gnl\|CDD\|370057	pfam08681, DUF1778, Protein of unknown function (DUF1778). This is a family of uncharacterized proteins. The structure of one of the hypothetical proteins in this family has been solved and it forms a helix structure which may form interactions with DNA.	8.60973e-16
NZ_CP036292.1\|WP_145122684.1\|5213792_5216807_-\|response-regulator	gnl\|CDD\|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	2.43393e-136
NZ_CP036292.1\|WP_145124239.1\|5197752_5198205_+\|cytochrome-c-nitrite-reductase-small-subunit	gnl\|CDD\|274453	TIGR03153, cytochr_NrfH, cytochrome c nitrite reductase, small subunit. Members of this protein family are NrfH, a tetraheme cytochrome c. NrfH is the cytochrome c nitrite reductase small subunit, and forms a heterodimer with NrfA, the catalytic subunit. While NrfA can act as a monomer, NrfH can bind to and anchor NrfA in the membrane and enables electron transfer to NrfA from quinones. [Energy metabolism, Electron transport].	4.56324e-61
NZ_CP036292.1\|WP_145122683.1\|5211027_5213664_-\|malto-oligosyltrehalose-trehalohydrolase	gnl\|CDD\|200464	cd11325, AmyAc_GTHase, Alpha amylase catalytic domain found in Glycosyltrehalose trehalohydrolase (also called Maltooligosyl trehalose Trehalohydrolase). Glycosyltrehalose trehalohydrolase (GTHase) was discovered as part of a coupled system for the production of trehalose from soluble starch. In the first half of the reaction, glycosyltrehalose synthase (GTSase), an intramolecular glycosyl transferase, converts the glycosidic bond between the last two glucose residues of amylose from an alpha-1,4 bond to an alpha-1,1 bond, making a non-reducing glycosyl trehaloside. In the second half of the reaction, GTHase cleaves the alpha-1,4 glycosidic bond adjacent to the trehalose moiety to release trehalose and malto-oligosaccharide. Like isoamylase and other glycosidases that recognize branched oligosaccharides, GTHase contains an N-terminal extension and does not have the conserved calcium ion present in other alpha amylase family enzymes. The Alpha-amylase family comprises the largest family of glycoside hydrolases (GH), with the majority of enzymes acting on starch, glycogen, and related oligo- and polysaccharides. These proteins catalyze the transformation of alpha-1,4 and alpha-1,6 glucosidic linkages with retention of the anomeric center. The protein is described as having 3 domains: A, B, C. A is a (beta/alpha) 8-barrel; B is a loop between the beta 3 strand and alpha 3 helix of A; C is the C-terminal extension characterized by a Greek key. The majority of the enzymes have an active site cleft found between domains A and B where a triad of catalytic residues (Asp, Glu and Asp) performs catalysis. Other members of this family have lost the catalytic activity as in the case of the human 4F2hc, or only have 2 residues that serve as the catalytic nucleophile and the acid/base, such as Thermus A4 beta-galactosidase with 2 Glu residues (GH42) and human alpha-galactosidase with 2 Asp residues (GH31). The family members are quite extensive and include: alpha amylase, maltosyltransferase, cyclodextrin glycotransferase, maltogenic amylase, neopullulanase, isoamylase, 1,4-alpha-D-glucan maltotetrahydrolase, 4-alpha-glucotransferase, oligo-1,6-glucosidase, amylosucrase, sucrose phosphorylase, and amylomaltase. Glycosyltrehalose Trehalohydrolase Maltooligosyltrehalose Trehalohydrolase.	0
NZ_CP036292.1\|WP_145122676.1\|5195777_5196296_-\|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.	2.45281e-05
NZ_CP036292.1\|WP_145122680.1\|5201402_5201999_+\|AAA-family-ATPase	gnl\|CDD\|226648	COG4185, COG4185, Uncharacterized protein conserved in bacteria [Function unknown].	2.55386e-55
NZ_CP036292.1\|WP_145122675.1\|5193372_5195427_-\|exo-alpha-sialidase	gnl\|CDD\|271234	cd15482, Sialidase_non-viral, Non-viral sialidases. Sialidases or neuraminidases function to bind and hydrolyze terminal sialic acid residues from various glycoconjugates, they play vital roles in pathogenesis, bacterial nutrition and cellular interactions. They have a six-bladed, beta-propeller fold with the non-viral sialidases containing 2-5 Asp-box motifs (most commonly Ser/Thr-X-Asp-[X]-Gly-X-Thr- Trp/Phe). This CD includes eubacterial and eukaryotic sialidases.	2.2502e-98
NZ_CP036292.1\|WP_145122681.1\|5201995_5202196_+\|hypothetical-protein	gnl\|CDD\|224662	COG1748, LYS9, Saccharopine dehydrogenase and related proteins [Amino acid transport and metabolism].	0.00673074
NZ_CP036292.1\|WP_145122685.1\|5217297_5218932_+\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.3449e-43
NZ_CP036292.1\|WP_145124241.1\|5202335_5208236_-\|hypothetical-protein	gnl\|CDD\|380081	pfam17973, bMG10, Bacterial Alpha-2-macroglobulin MG10 domain. Alpha-2-macroglobulins (A2Ms) are plasma proteins that trap and inhibit a broad range of proteases and are major components of the eukaryotic innate immune system. However, A2M-like proteins were identified in pathogenically invasive bacteria and species that colonize higher eukaryotes. Bacterial A2Ms are located in the periplasm where they are believed to provide protection to the cell by trapping external proteases through a covalent interaction with an activated thioester. This domain is found on the C-terminal region in A2Ms in bacteria. Structure analysis of Salmonella enterica ser A2Ms (SA-A2Ms) show that they are composed of 13 domains, all of which fold as variants of beta sandwiches with the exception of the TED, which consists of 14 alpha helices. Most of the beta sandwich domains appear to serve a structural role and are referred to as the macroglobulin-like (MG) domains. This is the MG10 domain. MG10 is markedly different from the other MG domains in that it has more beta strands and an alpha helix. The position of MG10 is stabilized by, in addition to other hydrogen bonds, the formation of a beta sheet with MG9.	5.56723e-31
NZ_CP036292.1\|WP_145124242.1\|5218939_5220292_+\|response-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	1.93873e-175
NZ_CP036292.1\|WP_145122679.1\|5198322_5199894_+\|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552	gnl\|CDD\|349426	cd00548, NrfA-like, cytochrome c nitrite reductase and similar proteins. This family contains cytochrome c nitrite reductase (also known as cytochrome c552, or NrfA) and similar proteins. The pentaheme enzyme NrfA catalyzes the electron reduction of nitrite to ammonia in the nitrogen cycle. This enzyme can also transform nitrogen monoxide and hydroxylamine, two potential bound reaction intermediates, into ammonia. It is a homodimer, with each monomer containing four classical CXXCH type heme-binding sites along with an alternative CXXCK heme-binding motif, which is important for catalysis. This family also includes octaheme nitrite reductase (TvNiR) from the haloalkaliphilic bacterium Thioalkalivibrio paradoxus which catalyzes the reduction of nitrite and hydroxylamine to ammonia as well as the reduction of sulfite to sulfide.	0
NZ_CP036292.1\|WP_145122690.1\|5223788_5224520_+\|phospholipase	gnl\|CDD\|224495	COG1579, COG1579, Zn-ribbon protein, possibly nucleic acid-binding [General function prediction only].	5.84472e-17

>NZ_CP036292.1|WP_145124241.1|5202335_5208236_-|hypothetical-protein
MNKGLPKTAIEALQPIIDGALQDKAYAEAVKAISQRIALEGAIQGDKPEEKVTRMTAEIEKAPEPMRPVMQAILANWYWQYFQQNRWRFMQRTETATSPSDDFTTWALPQILAEIDKHFRLALAAPEALQKTPIDQYDALLNKGTAPDAYRPTLYDFLVFDAIDFYAAGEQAGARSQDAFDLQADSPIFASAADFIAWEPPTDDAKSPTLRAITLYQDLLVFHQDDDDKSAFYDADLSRLVFGNNKAFGEEKSSRFKASLKRFIEATAGHEISARGNAQLAQTIRDEGDLVEAHKIASEGLENFPKSVGGALCFNLIQQIEARSAQVSTERVWNEPLSTIDVQYRNVTKIYFRLVPFDFEAFVQSERWNSEQLDQRQQQELLARTPVTAWNADLPATTDYQERVEELPTPDDLKPGAYYLIASHHPEFVRADNQVSFTEIWVSDLALVLRNHNGDGFVDGFVLDARSGDPLANANVRAWQRTNHGNRRQPLPSTKTDENGRFEFRGQRLRGMVFHVVDGDNALSSIHNVDSYQNNRQPRPDEQTRFFTDRSIYRPGQTIQYKGICLRVDQQKDDYATIAGRELTVVFNDVNGKEIQRQKHRTNDYGSFSGSFNAPRDRLMGRMSIHVAGEPNGATQVTVEEYKRPKFLVSLDAPKEAARLGGEVNLQGSAKAYTGAAIDAAEVRWRVVREVRYPIWWSWRCWWIPQVPDAGQEIAHGTTTTAADGSFDIRFDARPDPSVSPESEASFQFTIYADVVDTTGETRSGSRQVNVGFVALRASVSSDDWQTTDAPTKIQLSTTTLDGEAIAADGVLKVYALQQPERPARGRLSNQPRPMYGRAGSPIDLADAPKPDPANPNSWALGEVAFEKAIQIDASGQAEAEVQLKAGIYRAVFETKDRFSKSVTALLPIQVLDPNAKQLSIKIPNLLASAAWSVQPGSEFEGVWGSGYDTARAFVEIEHRGGVLQSFWTAPGVTQVQIKQPIEEGMRGGLTLRTTMVRENRAYLESWQIRVPWTNKQLTVRWEHFVSKLEPAEKQTWTAVIDAPDAKRAAAEMVAGMYDASLDAYLPHHWADGFHVFRHNRSNVYSQFENQQKQLQGLLFNWNVDARDASLIYRSFPGEIINAIYGMRGNVQFRSRRGGGIAGGLGMMEADSFAGAAPAPMAMAKGMAKDSNAQVASAPAAEGAPADDQPPAAEVDLENVSARKNLNETAFFFPHLIAGDDGTVRMEFTMPEALTKWRFMGFAHDNELRSGLLTDTVVTAKDLMVQPNPPRFVREGDVLEFTVKVSNQSPTRQTGTVRLSFAEARTGDSVDAAIGNDQRDQAFEIAAGQSKSLAWRIQIPDGIGFLTYKAVGSTGRLSDGEEGYLPVLSQRVLVTESQTLPIRGPQTVEFDFEKLLKSGDSDSLRHQSLDVQMVSNPSWYAVMALPYLMEYPHQCSEQTFSRLYANALARHIAGSDPKIHRVFEQWRGTPALESPLMKNQDLKAVMIEETPWLRQAESESEARRNVGILFDDNRLNDETARLLKKLADQQLDDGAWPWFPGGPANDYITLYITTGFGRMRHLGVDVDTSAAVKSLTRLDAWVTKQYTNIAESNRDDNHLTATIALYLYGRSFFLEDQPVAAEHRTAVLYWLQQAKQYWLKLNNRQSQAHLAVALKRFGDLKTPVGIMASIKERSVSDEEMGMFWRDTEESWWWYRAPIETQAMMIEAFDEVMDDAAAVEDCKVWLLKQKQTQDWKTSKATADAVYALLLRGTDLLASSELVRVDLGGQTVEPKDVEAGTGFYEQRFSGAEVTPQQGKITVTKVDEGVAWGSVTWQYMEEIAKITPHDGTPLTLTKQLFVKETTKDGPVLKPVDGPIAVGDELVVRIVLKTDRDMEYLHLKDQRGSGTEPVNVLSRYKYQDGLAYYESTRDTASHFFIDYLPKGTYVFEYSTRVQLRGRYQSGFANIQCMYAPEFNSHSESLLLEVQ
>NZ_CP036292.1|WP_145122681.1|5201995_5202196_+|hypothetical-protein
MIRDNTPELVRKANAAMQQAADDVLVRARQHNTPIVLWRDGKVVEVDPFSEEFDPPSKEPPAAGTE
>NZ_CP036292.1|WP_145122680.1|5201402_5201999_+|AAA-family-ATPase
MSSPPQPTVYVIAGPNGAGKTTFASRYLPNFAGCQEFVNADLIASGLSPFNPESQSVAAGRLMLNRIESLTRKGTSFGFETTLAGRGHVKRLRMMKKLGYRVSLFFIWLPSVDLAVARVATRVREGGHNIPEPHIRRRYQLGINNFASLYKPVLDEWVIYDGSSRPGEIIVGEQDNVRRVYDDARFAELKQLSPELMR
>NZ_CP036292.1|WP_145124240.1|5200248_5201250_+|hypothetical-protein
MGQSSPSALTFNDPNPQRYQFKARASELDPRVQAHPEIGFLIDNKDGKPADFQQAAVDTRVAPKGKLVIWLMGHNQGLFDRWNSYGLHAIRVHYANKWFSICCRENPVGEECRGNIRLEAATGEDFSSDVDIPKPDGMMERALKFVQWLAKENPQGGWDYFLTEDGNGLRWEDVIMSGSSHGSTTAARFAKHQKVSRVVALCGPRDNYQTWQSLPSATPENRYFGFSHVLDGGWTADHYCRSWEMLGMNKFGPIVNVDKIGPPYQNTRRLITDFDVDGNARRAHSSVQPGGSAGKDADGKYIHEAVWKYLYTHPVDVVGEATPPDASCIKNQR
>NZ_CP036292.1|WP_145122679.1|5198322_5199894_+|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552
MTTSDNRSRSLGWLALLTGTVAATTFGVVAILVNIFERKQEARTPFVRVVEVDEVSTDPKPWGLNFPQQYEDYLKTVDDEYTDYGGNHALPPSKLEEYPWLKRLFAGYAFSIEYREARGHAHMLADQEVTRRVTEVQQAGACLHCHASIIPTYRRIGMEELGQEVTAAKLAESFNQEAVMAGFKAVSQRTYEEVHAELEKTPDGVVEAAAGDPHLGNAHPVSCIDCHDPKTMALRVTRPGFLIGIDKLAKSDDPVPHLPSIAKWRKAGSKGTYDPNTDATRQELRSFVCGQCHVEYYCANKMTLTFPWSHGLKVEDLEAEWDSTTFPSEEADETGEPFYDYVHKETGTKVYKAQHPEFELWSQGIHARAGVSCADCHMPYEKVGATKVSSHWVRSPMANINKACQTCHKVSEQEIKDRVDLIQHRTSDLIDRAAAAVTEMFDAIIAAREAGASDEQLKPIRDLQRKAMWRLDFIASENSKGFHASQESARILAESIDYSRQAIAGCYQLESEPAAEPAESDAS
>NZ_CP036292.1|WP_145124239.1|5197752_5198205_+|cytochrome-c-nitrite-reductase-small-subunit
MRFGKVAMTFFVCLGLLAGVGTFTFGYGKGASYLSNNPETCINCHVMQDHMDSWQQSSHHHVAVCNDCHLPHDFVGKWVTKADNGFFHSLAFTMGGYKDPIQIKPRNQRVTQSTCISCHKDFVHPLLPATAGHDMLSCVHCHADVGHAGR
>NZ_CP036292.1|WP_145122678.1|5196831_5197311_-|DUF1772-domain-containing-protein
MSPFSFLESLTILAIAGCGLMAGLFFVFSVAVMQALSQLSSAEGLNAMQSINRTILNSVFLTVFFGTAIVCLGLIVCSLGQRQPGWQWAIAGASTYLVGGFVVTATRNVPMNNQLEQFSEPSPRAIEYWRTYQSLWTRWNHVRTIASASAVVMLVISLL
>NZ_CP036292.1|WP_145122677.1|5196296_5196575_-|DUF1778-domain-containing-protein
MATTKNDARINVRLASELKQVIEEAATALGQTVSEFTVSTVVREARQVIQEAQFTRLSTRDRDAFLGALRAADAKPNDALKAAARRYKKRIG
>NZ_CP036292.1|WP_145122676.1|5195777_5196296_-|GNAT-family-N-acetyltransferase
MGNVWGIEPFERKKHVRTGFDCGVAVLNDWLATKISQYEKRDLARTYVLVGDGGNAVKGYYALSNHTVVYEALAKDQARGLPQIDLPVVLIGRLAVDTTVRGQGLGEFLLLDALRRVEYLAAKIGIQAVEVDAINDRAKQFYLKYGFTPLQDNPSHLFLPMQVVRKLRLPPL
>NZ_CP036292.1|WP_145122675.1|5193372_5195427_-|exo-alpha-sialidase
MTTSCAFPSRWFWAILCILSLVGSVSADEAARDSGADSGSRTTSFEEVKSGRFEKLDTNLGNWTSDSGVASVSARHAHSGRQALHLAGGEKTVVRLRLPDAVDTSGTLSFRAERWTQRAPFTFRVEKKAGDDWAEIFRGDDVVRVGRSFLSHVIVPINDDSVEQLRFTCTSPADAGILIDDLTIGPAEPQKVTNVELVPFSLPALVGTQSSSLVKLKVEVTGILDPISIVELRARVVGVQQIESLQVGDGEPVELADNAATTLQTSQPLEQGENIVWLRCRLREDANIDRQVGATIEQVKFSNGETVELDSPIQRQRMGVAMRQHGDDDVHTYRIPGLATTNRGTLIGVYDIRHRSGRDLPGDIDVGMSRSTDGGRTWEPMKTIIDMGDDPKWKYDGVGDPAVLVDRNTGTIWVAGTWSHGDRAWRGSGQGLAPEETGQLMLVRSDDDGLTWSLPINITEQIKRPQWCFILQGPGKGITMRDGTIVFAAQYQDPPEQQRLPHSTIIYSKDHGETWHVGTGAFDDTTEAQVVEVEPGVLMLNCRYNRDSARVVMTTHDMGKTWQKHPTSELALIEPQACMASLIDADREVGRDVGGWLLFSNPNSLRGRNHITIKASADRGSTWPKQHQVLLDEGNGAGYSCMTMIDEKTVGILYEGSQAQLTFQRIPLSDIVSPIGSTTNSGDE
>NZ_CP036292.1|WP_145122682.1|5209967_5211005_-|ABC-transporter-substrate-binding-protein
MNRTLSPITAARLKSVSLMICIALLLSGCSSSSDSSAGGSTSEASGLQQVSLQLNWFPEAEHGGYYAADVHGFFADEGLEVTLLPGGPNVPVVQSVAAGRAAFAVTNADRVLFGHQAGAEVVALFAPIQNTPRCIMVHRESGISKLADLRDVTLAIGTGPAFFQYMQKHLPLTGVETIAYPGSIGPFLANKRFAQQAYIFSEPYVAKQQGADPVTLMVSEIGYNPYASVLVASRKTLDTQSDLAQRIVRASARGWQKYLDDPAETNAVIDSINPDMDAGALAFGAEQIRPLCDREDPAAPLGQMTAARWQTLIDQMVEIELVDADKVSAARVFDDRFITPTASQE
>NZ_CP036292.1|WP_145122683.1|5211027_5213664_-|malto-oligosyltrehalose-trehalohydrolase
MPIRPRSILATDLDGTLLPLQDDPTHIADLQTLLENLRDNDVQVIPVTGRDRAAMIEALQAFQIPAPEVAICDGGTTIVVRNDDGGFDYLPDFQTHLEANFASFATDDVSYLLRDLVDLRFRATEKQNQFKISYFAEAKTLQATVATIQSRLRDSGIDCDVISGFNLHWGEGLVDILPAGLSKAYALQWWLDRSGNDRDQVVFAGDGGNDLEVFLAGYRTIVVGNAEPEIASTVYAAHRTGNTLDRFYLSEARATSGVLEGCRWFELVPPEKQESRSSDPLGAVPVSCNATHFNIWAPYAGRLAIEKQNGDEVQRFRIQPDEDGYFHRTVRGIGGGDRYQISLDDRVSRPDPASRFQPQGVHGPSMVVDHRKYPWHDADYRGVAKSDLVIYEMHFGTFTSEGSYLAAIDRIEELVSLGITAVEVLPLAQCAGSRNWGYDGVQLYAATENYGTPDDFKRFVDACHAAGIAVILDVVYNHLGPEGNYLHDFGPYFSKRHHTPWGDAFNYDGENSEAARRFVIENAIYWLREYHLDGLRLDAVHFMFDDSDQPILRSIRHAVTDFAGTVDRPIHLIGEANIYDHALVSPTDGTAYDAIWADDIMHAIYSHTVPEINLAHRHYAGASDIEEALQHGYLHTGPKVTRIDSEVRRQMHAEGDFSFLPSLICGLQTHDCVGNHPHGSRFHQLTSTETQRAAIPLLMLYPSIPMIFMGEEYACDAPFMFFVDFGDPRLRRAVDRGRRNEYPHHQWKGAIAPSHGDAFAKSKSIQIKDAAIWQWYRDLIALRKTWQRESLLDWKNLSVLCDPTRSLFALQYQAPTGRPKFVVSRFSAPADDLPPLSLQIDGDVLMQSSVHRDSPTQLTLQNQAVLIGEGTWNLAAGQ
>NZ_CP036292.1|WP_145122684.1|5213792_5216807_-|response-regulator
MTDPTGPFDLQSALQKVRSRLVAQTDGFADEEELLAAWDQIARRAEAAESTFSQLPPQQPSEIFIDSQDPSSALGETRILYHTLVDNLPINLVLKDLHGRRVFANERYLQLHQMTLQELRGKTDFDIFPEHLAKAYQLDDQQVIREGIVLHDTEPYLAKDGNECWIERVKAPVRDAQGKITGVQLLFWDVTERKHLDQDLEKARYLLNTLLNNIPDSIYFKDRDSRFIRISRSMAKKFQWKNAEIAVGKTDADIFTSEHAANARASELEIMETGVPMVAEIERETWADRPDSWCSSTKMPLRDDAGRIVGTFGITRDVTDLKRTEQELKTAKEAADAANQAKSDFLANMSHEIRTPMNGIIGMADLMAHTNLSIEQRDYLRTIKDSADSLLRIINDILDFSKIEAGKLELEETSFNLRDCVGRTVQTLAVKAAEKGLELACRIDPHLPNQVAGDPVRLRQIVVNLVGNAIKFTQQGEVVVEVTNADDPKVIAITNPLANGQSHLPLEALDAGAIRLQFAVRDTGIGIPSEKVQTVFEEFAQADVSTTRQFGGTGLGLAISARLVDLMHGNIWLDSQVGVGTTFYFTAEFLLADAAVAPTENLDSLRGLPTIVVDDNNTNRQIFGEMLDAWQLNPTLVASAPAALAELQRAASTEDPYRLVLLDCMMPHMDGFALAECIRQSPLLKGLPIIMISSAARADDSQRCREMGIQRYLTKPVLQSDLFDSILDAMDIRSHHAASTPSLEPGGNQRPLNILLAEDGLVNQRVAIGFLSREGHNVTLARNGIEAVMEVARQPFDLVLMDLQMPEMDGVEATLEIRVRDRHLGIHTPIIAMTAAAMDGDRERCLNAGMDDYISKPINPSQLQAVIAGVFDREPPTAAAAPERFLPPLELANPTQIVDLRHAIERIDGGWELLEPLTSAMRQEGPILIDQIHHALQMGDCKSLARAAHTLKGSADVFAASRVVAVSIRLEELARANKLAECRALLDELQDEVEAMLEHLNRGA
>NZ_CP036292.1|WP_145122685.1|5217297_5218932_+|HAMP-domain-containing-protein
MLRNYKIRTKLLIALGLLCAIVLTISLGGFQSIYAYRQLASSISDRAAELPLTSSLTRDVELLRNTYHRIHDHSSSENPLARISLTNERDQFRTCVADVRSSANAYRGELDAGDDEATVLSDRSRERHTIDAMLRGLERIDDIVRAENWALKEIDYARLEIELDSLADSAQQLPTFLQQHMLSLRDDVRGFYRTAIAVMWGSSLLALGMFAALIFLFHLVVVKPFGSLLQGSRTISEGVFAHRIELGTGDELAELANSMNDMTARFLSTESELKDVIAGKEEEIRNRTNEAIRNEQLASVGFLAAGVAHEINNPLASIAWSAEALESRLHDQLYDTDSDGPSQPLNNDQLSTLRTNLRRIQDEAFRCKGITEHLLDFSRLGNVKREPTDLKHLVEDVVAMVGTLGQYRCKTIRLDCPDEVNAAINGQEIKQVVLNLLTNALESVDTDGAIDVRLRQRGDVAVLTVEDDGCGMDEHVQNHLFEPFFTSGKEGQGTGLGLSISYRIVQQHGGRMSAQSEGRGRGARLDVTLPLEHTMEADVQKNAA
>NZ_CP036292.1|WP_145124242.1|5218939_5220292_+|response-regulator
MSIMFADDEPGLQELMAAELPRLGHTVTVCPDGLTALAAVEKQAYDCIIVDLDMPGMNGIEVLQRTKELQPLCEAIVLTGKSTTESAIIAVKCGAFDYLTKPSRLADLATLLGRVAERRQISKQMSALQLRLRRAEGDPQLIGKHPSMERVAKLIAKVAPTESTVLIRGETGCGKELVARAVHDQSRRAAESFVAINCGALPENLIESELFGHCRGAFTGADAARTGMFQVADGGTIFLDEIGELPLSMQAKLLRVLESREIRRVGDNQVEKIDVRVVCATHRNLEQMVEQGEFREDLMFRINTFEIEVPSLRERASDIPELAAHLLRRFNNEQLSDAELFTPETMSALTAHVWPGNVRELANVIEHAVILCDALPIRPEHLPRHFGDRQLRKELRSSGPMSLREMEHVAIEQALERHDGNKSAVAAELGISLKTLYNKLNTVAAEKQSA
>NZ_CP036292.1|WP_145122686.1|5220341_5220755_+|hypothetical-protein
MNTDSASLRSSDIELVEPTPQLRIVSDSEAAELAAEIPTGSPFAPGTALPLDLVGQPISFEAGVWRETMLGGLLASLIMIAFGIGSLPIFPVGSMLIAGGGCLLGAMALVTRRPMLAMAATIGNLAVLALGFVRSFW
>NZ_CP036292.1|WP_145122687.1|5220811_5221951_-|transglutaminase-domain-containing-protein
MDCAACSERSGRRPTAAAEIRFVPTRIRPRPMKSSIDPRRQSDARRSMARDDRRSFPIAPLSITRRTMLLSGAACCASPLLAQDSSSPVADTRLEYVGPEKQLWQVGVKVMTAGSSCEEIFATFPVPTDWPEQTVQLVDQQISRYVDRWDTRDLFGGAKQVRVRMVNVPANTASDALFTFEVTKTRIQGVGETSDLVVPQKVEREERVFLGSSPYIDPRHGKIRKIAAEFESTPDQTPWQQVEQIYDWVREHVEYREGDIKSAVEALDDGHGDCEELTSLFVALCRAKKIPARMVWIPGHCYPEFMLHDPEGVPHWFPCQAAGTRQFGEMDEYKPILQKGDRFKVPEQKALQRYVAEFCKVKARSKPDVTFVRELTDSE
>NZ_CP036292.1|WP_145122688.1|5222080_5222467_-|hypothetical-protein
MNARFVTLVAAVSLAALTGCTGIGNGFCGGNLGAPCGAGCAAAVNPAYDYAPTPEPGCGCGTDAYSGYSTGGYYEGMGSYSEPSYQGGWQSSQGVPQPGQYSDGGYVVPNGPGTNMAPAPTLPQPNNQ
>NZ_CP036292.1|WP_145122689.1|5222560_5223658_+|alpha/beta-hydrolase
MRFFCNIIVRFDATEKGAVRFVNIPRSSNVVDAMHSMSSRSIATLGVVLLLTVLSSSVSHAALLREGDEYWVLNSRCISSVACRANLENPNLKVYRYHQGQGLQHDSVNGLYTRVDEDHSFLNVIYVHGNRFTSQEAIDRSLKIYRSVNRRCHDQTRIRWILWSWPSDPIFNPLTDVRTKAQRADTQALYVGWLLQHFPAPDRLEMIGYSFGGRIVTGALHTAAGGEMKGRTLSGPPLRGSRIGIHLVAPALDRHWLASGSRHGLAAENIGSMNLFYNSRDRVLKLYSMVSKYYNPVALGFAGLGQLAARSDHLPIQIRARDCGGAVGLLHDELKYFEPCCNVAETIATTLDASDSEVIQLTAAD
>NZ_CP036292.1|WP_145122690.1|5223788_5224520_+|phospholipase
MSDAPHKISHSTISTLHHIHKKLTELNSQIGRGPRQLKAGIAAIESLKQAELQAQETLKQAKLACDSKQLQLKEREQRVVDIQNKLNTAASNREFQTFKEQIAADQQANGVLADEILEAMEKIDRLGEELRQRTAELKQRSDDHAKLQSEVDARVATASSERDRVLEELATAEEQLPEDAVDIYQRLIRSQGEDGLAPVEGQSCGNCGATFAPQVLNRLMLSHFICCPTCGAILYMTADSVPE

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Crispr_ID: NZ_CP036292_21

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_21

5268695-5268797

Orphan

Consensus_repeat	Method
GCCTTACTGGCCCCGGCGGCTTACACCGCCGGCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_21

>merge|NZ_CP036292|21|5268695-5268797|CRISPRCasFinder
GCCTTACTGGCCCCGGCGGCTTACACCGCCGGCAGTTCGTGTGTCGGCCTTCGGCCTGGGTTCCAGTGCGCCTTACTGGCCCCGGCGGTTTACACCGCCGGCA

>NZ_CP036292|21|21|5268695-5268797|CRISPRCasFinder
GCCTTACTGGCCCCGGCGGCTTACACCGCCGGCA	GTTCGTGTGTCGGCCTTCGGCCTGGGTTCCAGTGC
GCCTTACTGGCCCCGGCGGTTTACACCGCCGGCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145122709.1\|5253242_5256056_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369375
NZ_CP036292.1\|WP_145122715.1\|5267151_5267880_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145124247.1\|5268143_5268629_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|226472
NZ_CP036292.1\|WP_145122720.1\|5276407_5277451_+\|EamA-family-transporter	unknown	unknown	gnl\|CDD\|307170
NZ_CP036292.1\|WP_145122717.1\|5270229_5272917_-\|azurin	unknown	unknown	gnl\|CDD\|274225
NZ_CP036292.1\|WP_145122723.1\|5279485_5279710_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122722.1\|5278756_5279323_+\|stage-V-sporulation-protein-G	unknown	unknown	gnl\|CDD\|377202
NZ_CP036292.1\|WP_145124248.1\|5275121_5276081_-\|flagellar-motor-switch-protein-FliG	unknown	unknown	gnl\|CDD\|235561
NZ_CP036292.1\|WP_145122711.1\|5259773_5261153_-\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|369346
NZ_CP036292.1\|WP_145122708.1\|5251703_5253005_-\|twin-arginine-translocation-signal-domain-containing-protein	unknown	unknown	gnl\|CDD\|223745
NZ_CP036292.1\|WP_145124246.1\|5250426_5251272_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|379207
NZ_CP036292.1\|WP_145122710.1\|5257221_5259696_-\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377876
NZ_CP036292.1\|WP_145122719.1\|5274162_5275125_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379829
NZ_CP036292.1\|WP_145122721.1\|5277760_5278723_+\|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase	unknown	unknown	gnl\|CDD\|224858
NZ_CP036292.1\|WP_145122714.1\|5266447_5267155_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|334031
NZ_CP036292.1\|WP_145122713.1\|5264681_5266202_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273435
NZ_CP036292.1\|WP_145122724.1\|5279804_5280968_-\|Na/Pi-cotransporter-family-protein	unknown	unknown	gnl\|CDD\|162157
NZ_CP036292.1\|WP_145122712.1\|5261313_5264148_-\|excinuclease-ABC-subunit-UvrA	unknown	unknown	gnl\|CDD\|223256
NZ_CP036292.1\|WP_145122716.1\|5269129_5270116_+\|zinc-binding-dehydrogenase	unknown	unknown	gnl\|CDD\|176228
NZ_CP036292.1\|WP_145122718.1\|5273061_5273829_-\|leucine-rich-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|378953

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145122709.1\|5253242_5256056_-\|hypothetical-protein	gnl\|CDD\|369375	pfam07462, MSP1_C, Merozoite surface protein 1 (MSP1) C-terminus. This family represents the C-terminal region of merozoite surface protein 1 (MSP1) which are found in a number of Plasmodium species. MSP-1 is a 200-kDa protein expressed on the surface of the P. vivax merozoite. MSP-1 of Plasmodium species is synthesized as a high-molecular-weight precursor and then processed into several fragments. At the time of red cell invasion by the merozoite, only the 19-kDa C-terminal fragment (MSP-119), which contains two epidermal growth factor-like domains, remains on the surface. Antibodies against MSP-119 inhibit merozoite entry into red cells, and immunisation with MSP-119 protects monkeys from challenging infections. Hence, MSP-119 is considered a promising vaccine candidate.	2.10953e-05
NZ_CP036292.1\|WP_145124247.1\|5268143_5268629_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|226472	COG3963, COG3963, Phospholipid N-methyltransferase [Lipid metabolism].	2.73665e-32
NZ_CP036292.1\|WP_145122720.1\|5276407_5277451_+\|EamA-family-transporter	gnl\|CDD\|307170	pfam00892, EamA, EamA-like transporter family. This family includes many hypothetical membrane proteins of unknown function. Many of the proteins contain two copies of the aligned region. The family used to be known as DUF6. Members of this family usually carry 5+5 transmembrane domains, and this domain attempts to model five of these.	0.000723947
NZ_CP036292.1\|WP_145122717.1\|5270229_5272917_-\|azurin	gnl\|CDD\|274225	TIGR02604, Piru_Ver_Nterm, putative membrane-bound dehydrogenase domain. All proteins that score above the trusted cutoff score of 45 to this model are large proteins of either Pirellula sp. 1 or Verrucomicrobium spinosum. These proteins all contain, in addition to this domain, several hundred residues of highly variable sequence, and then a well-conserved C-terminal domain (TIGR02603) that features a putative cytochrome c-type heme binding motif CXXCH. The membrane-bound L-sorbosone dehydrogenase from Acetobacter liquefaciens (Gluconacetobacter liquefaciens) (SP\|Q44091) is homologous to this domain but lacks additional sequence regions shared by members of this family and belongs to a different clade of the larger family of homologs. It and its closely related homologs are excluded from the this model by scoring between the trusted (45) and noise (18) cutoffs.	2.12222e-59
NZ_CP036292.1\|WP_145122722.1\|5278756_5279323_+\|stage-V-sporulation-protein-G	gnl\|CDD\|377202	pfam04026, SpoVG, SpoVG. Stage V sporulation protein G. Essential for sporulation and specific to stage V sporulation in Bacillus megaterium and subtilis. In B. subtilis, expression decreases after 30-60 minutes of cold shock.	1.19047e-34
NZ_CP036292.1\|WP_145124248.1\|5275121_5276081_-\|flagellar-motor-switch-protein-FliG	gnl\|CDD\|235561	PRK05686, fliG, flagellar motor switch protein G; Validated.	5.91008e-92
NZ_CP036292.1\|WP_145122711.1\|5259773_5261153_-\|DUF1501-domain-containing-protein	gnl\|CDD\|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	2.38961e-117
NZ_CP036292.1\|WP_145122708.1\|5251703_5253005_-\|twin-arginine-translocation-signal-domain-containing-protein	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	6.74862e-25
NZ_CP036292.1\|WP_145124246.1\|5250426_5251272_-\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|379207	pfam13472, Lipase_GDSL_2, GDSL-like Lipase/Acylhydrolase family. This family of presumed lipases and related enzymes are similar to pfam00657.	1.35262e-11
NZ_CP036292.1\|WP_145122710.1\|5257221_5259696_-\|DUF1553-domain-containing-protein	gnl\|CDD\|377876	pfam07587, PSD1, Protein of unknown function (DUF1553). A family of proteins found in Rhodopirellula baltica.	2.2145e-50
NZ_CP036292.1\|WP_145122719.1\|5274162_5275125_+\|hypothetical-protein	gnl\|CDD\|379829	pfam16344, DUF4974, Domain of unknown function (DUF4974). This family consists of uncharacterized proteins around 340 residues in length and is mainly found in various Bacteroides and Parabacterodies species. The function of this protein is unknown.	0.0038227
NZ_CP036292.1\|WP_145122721.1\|5277760_5278723_+\|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase	gnl\|CDD\|224858	COG1947, IspE, 4-diphosphocytidyl-2C-methyl-D-erythritol 2-phosphate synthase [Lipid metabolism].	1.5248e-68
NZ_CP036292.1\|WP_145122714.1\|5266447_5267155_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|334031	pfam00359, PTS_EIIA_2, Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2.	1.96259e-21
NZ_CP036292.1\|WP_145122713.1\|5264681_5266202_-\|hypothetical-protein	gnl\|CDD\|273435	TIGR01085, UDP-N-acetylmuramyl-tripeptide_synthetase, UDP-N-acetylmuramyl-tripeptide synthetase. Most members of this family are EC 6.3.2.13, UDP-N-acetylmuramoyl-L-alanyl-D-glutamate--2,6-diaminopimelate ligase. An exception is Staphylococcus aureus, in which diaminopimelate is replaced by lysine in the peptidoglycan and MurE is EC 6.3.2.7. The Mycobacteria, part of the closest neighboring branch outside of the low-GC Gram-positive bacteria, use diaminopimelate. A close homolog, scoring just below the trusted cutoff, is found (with introns) in Arabidopsis thaliana. Its role is unknown. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	5.00495e-47
NZ_CP036292.1\|WP_145122724.1\|5279804_5280968_-\|Na/Pi-cotransporter-family-protein	gnl\|CDD\|162157	TIGR01013, Sodium-dependent_phosphate_transport_protein, Phosphate:Na+ Symporter (PNaS) Family. [Transport and binding proteins, Cations and iron carrying compounds].	9.30271e-41
NZ_CP036292.1\|WP_145122712.1\|5261313_5264148_-\|excinuclease-ABC-subunit-UvrA	gnl\|CDD\|223256	COG0178, UvrA, Excinuclease ATPase subunit [DNA replication, recombination, and repair].	0
NZ_CP036292.1\|WP_145122716.1\|5269129_5270116_+\|zinc-binding-dehydrogenase	gnl\|CDD\|176228	cd08267, MDR1, Medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family. This group is a member of the medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, but lacks the zinc-binding sites of the zinc-dependent alcohol dehydrogenases. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P)-binding Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability. ADH-like proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and generally have 2 tightly bound zinc atoms per subunit. The active site zinc is coordinated by a histidine, two cysteines, and a water molecule. The second zinc seems to play a structural role, affects subunit interactions, and is typically coordinated by 4 cysteines.	4.34707e-90
NZ_CP036292.1\|WP_145122718.1\|5273061_5273829_-\|leucine-rich-repeat-domain-containing-protein	gnl\|CDD\|378953	pfam12799, LRR_4, Leucine Rich repeats (2 copies). Leucine rich repeats are short sequence motifs present in a number of proteins with diverse functions and cellular locations. These repeats are usually involved in protein-protein interactions. Each Leucine Rich Repeat is composed of a beta-alpha unit. These units form elongated non-globular structures. Leucine Rich Repeats are often flanked by cysteine rich domains.	3.14566e-05

>NZ_CP036292.1|WP_145124247.1|5268143_5268629_+|methyltransferase-domain-containing-protein
MVGWFDWESARGVVEYGPGTGVFTKHVVQKLHPDAKFFAIERDPELVAIVQQKLPDVDVVEESVANVVALCQARGIEQVDAIVCGLPWASFPDTLQRECIDAMMQVLRPGGQFATFAYWQGLLLPAGQRFKRRLGDYFSTVEYSPTVWRNLPPAFVYRCTR
>NZ_CP036292.1|WP_145122715.1|5267151_5267880_+|hypothetical-protein
MMLWIGDNQHPEFRDAWTWASQSGQCQHRDSIDAAVEQPVARSTPRIVIARPDRQPPPAAAFNALQQQYPLASYATLLGSLCEGEQRTGTPWPHCQRIYWHRWSFQLVAWSGLNPQASTSAPATSGCIGIVSRSRWIGSGVVDSLRHANIPCVAVAPQQLAVAGPYSDLLWDDSVIATLDDWQAQAAAVAAHAGTARHHWLVSSPRVETWHALQAAGFESLHSKPLDLDSILDSLNRRTATA
>NZ_CP036292.1|WP_145122714.1|5266447_5267155_+|helix-turn-helix-domain-containing-protein
MSEENFDVAGLAAYLHLTPDQVNKMAQRGRLPGRRVSGGWIFSEAEVHHWLEQQIGASDLEQLDKVDAVLSRADSIDEEITIASFCSLDVIEVPLQARTKGSVIRSMSALAARGGMLWDPAAMAEAVKAREELHPTALDCGVALLHPRRPQTSILADSVVALGRTSQPLPFSDTGQLTDVFFLLASYDDRVHLRILSRISRMITDEIFLGQLREAPDAASARQAILDVEERIDEV
>NZ_CP036292.1|WP_145122713.1|5264681_5266202_-|hypothetical-protein
MDVAKRIGSQDVSLRQLFPAARMISTPDITVRRCSADASDCSPGDVFVVGIDDIPADEAAAEAVAGGAIGIITEQLLPVSVPQCIVADAREAYAHLVSELAGKPSQQMLSIGVAGIDGKTSTTLMVAAALRKSGLRVAYNCDLGRSDGIVQDVPRRPLSDAQDLTDWYADASDSGCQVAVVELSEAMLRSHAADGTSFDIMILSGDSDHAYLKSAQGGSLFNEAISHVRSKGLVILNESNAVAAQAAESSDLSILTYGTSQEADVVGRIMERHAGETTFLITAGDTTAAVRSRMTGDWMFHHQLAAAATALVMDFPLETVAAGLSAMEKIPGRMQRVASYTGPQIVLDDADCPERVMATINTLRKELPRRGKIWCIAACDHRRTATHAANLGYITERCSDHLVLTSGVSGTDEFLSLVHEMLDGVVDPAKPQLIANREAAIQWTINKATPNDLVVILGGWCPDSPRTIRAAIDADTKLAEQALERVEASDDSEPVILPHPALLASM
>NZ_CP036292.1|WP_145122712.1|5261313_5264148_-|excinuclease-ABC-subunit-UvrA
MNQRSIRLRGVRVHNLRDVDVDVPHHQLVVFCGVSGSGKTSLALDTLYAEGQRRYIESFSAYTRQFLQRLDRPDCESIEGIPPAIAVTRGGASRSNRSTIGTATETADYLRLLFAKVADLTCLNCGQPVRSDDPQSAANQLAATEPAARAMLGFPLLLESKLHAVDELSYLQQQGFLRLIVGDRTFNLGDESRGELAEAIGDGAEAIVIVDRLKTADAAGRLTESMETAFAEGAGQAVALIESAEGETVVDGKSWRAMKWSRQRKCETCQIIYPDPEPRLFNFNNPLGACPACEGFGDIVDVDMDLVVPDRSKTLREGAIQPWNTPSYQHELEELLALADDYDLPVDVPFSRLTKKQRRLIDEGVPEREFGGLNGFFAWLERKKYKMHIRVFLSRWRSYRRCTTCNGQRLKDEVLAYRVGGKNIAEVCAMEVDAIAQFFADVKLADREAEIADDVLHQVRNRLGYLQSVGLGYLQLDRTLRTLSGGEAQRVALTSALGSSLVNMLYVLDEPTAGLHPADVPSLIESILRLRDRGNTVAVVEHNEAVFTAADRLIEVGPGAGASGGEIVFEGTADEMVETQGSLTGDYMSGRRGMLSLQRDRLQPRGWLKLTGASGNNLQSIDVDFPLGVLCVVTGVSGSGKSSLVHDTLYGAICRRKKKSGATSLPYTDLVGDGQLEDVLLVDQSPISRSPRSNPVTYVKAFDSIRKVFADTLEARTRNFGAGHFSFNSAAGRCEACEGDGMLQIDMQFLADIYMQCPECKGTRYRDEILKIRYRDRNIADVLKMTVRQAVSFFRGYDKVQEKLKRLTDVGLDYLQLGQPANTLSSGEAQRLKLAAFLSTAQRRRTLFLMDEPTTGLHVADIVKLLGCFDALLADGHSLIVVEHNLRLIKASDYIIDMGPGAAGNGGRVVAAGEPEVVKEVAESATGQILKRAIEADLAANEQV
>NZ_CP036292.1|WP_145122711.1|5259773_5261153_-|DUF1501-domain-containing-protein
MLDLIGRGKAQTCNGTTRRDFLQVGTLGMLGLGLPSYVAAREAGKVDPAKDDHSCIMIFNLGAPSQLDTFDMKPDAPAEVRGPFKPISTASGEFQISEILPQHAKIADKFSLVRSCFHRGAAVHDAGWQMMQTGRLFTGGVNYPHAGAVVDYLRGRRSDLPAHVVLPETMGRGGGNLPNGQAGGFLGKRYDPFALMADPSQPNFQVPDLLPPDSIGQARIDRRRKMREIVEQTMTNFESSETAQLLDGSFESAYRMMTSPEARNAFDLAKEPMKVRERYGMNRFGQCCLLARRLIEGGVRFVTINTFLTVFNEITWDTHGSKPFTSIEGMRDIVAPMYDQGYSALIEDLADRGMIDSTLVACLAEFGRTPKVNPAGGRDHWPQCFTTYFAGGGVQGGRAIGASDPNGAVPAERPAGADEVVATIFHSLGLDLDTELPGPAGRPFPLVNFGAREIHELFS
>NZ_CP036292.1|WP_145122710.1|5257221_5259696_-|DUF1553-domain-containing-protein
MQRIALLLTAALAFAPAALAQTTLRILPEKIELTGQEASQRFLVQQVVDGRVAGQITGGVDLKPKTDGLVRVADGRVIAVGEGQTELIATDAAGNTATAMVIVRLADVPQTIRFASDVQAVLAKASCNSGACHGALAGKGGFRLSLLGYDSQGDYFNISQQLRGRRVELADPARSLIVAKPSGMIPHKGGVRLPKESADYKLLLDWISAGAPGPADEDPTLAKIEVLPKAVRLAKGDTQQLVVRAHYSNGRIKDVTQWVRWSSTNDAAARVDDQGMVTVTGPGVGAITAWFASQIVIANVTVPYAQEVSDAQFAKLQPRNFIDREVLKQLKQLNIPPSDRAGESEFLRRAYLDTIGRLPSIDETLSYLADDSPDKRDQLIEQLLVQPEFVDYWSYRWSDILLVNGSKLRPKAVESFYKWIRSHVEAGTPWDVFVREILTSRGSSFENGATNFFANHQTPEEMTENASQAFLGLSIACAKCHNHPLEKWTNDQYYAMANLFARVRAKGWGGDSRNGDGNRTLVVLDRGDLIQPLIGKPQPPAPLDAPPMEIDDPADRREYLADWLTSPENPYFARSITNRVWANFFGVGLVESVDDMRVSNPASNEALLAAASKHLIDSGFDLKSLMRTILQSETYQRSSQSLPENAAEKRFYSHYYPRRLMAEVLLDAISDVTDAPTEFTQISFPGADMQQTDLYPKGTRALQLYDSAVASYFLQTFGRNTRDITCECERSDEPSVVQVLHLSNGDTINQKLAAKENRLSRWIADGLDDGTIIDQVFLAALSRQPTAQEREALLASLQGEEDRRQALEDLVWSVLSSSEFLLAH
>NZ_CP036292.1|WP_145122709.1|5253242_5256056_-|hypothetical-protein
MFATRTHHHFTAALLACFLLMPCVTGCTQLQLPAIDPTGECFFLPCPNTTTLTLPCTDKLQNGCGPFGCLPEPAFTDPAPPPPCLQGAGVPQTAPPPPPAKVVDECADGPKAVLFDKHCDLRKLLHLPDRGKRGRILLNHRKIIAPVGGEVVLLSGVCGTDGYLMTGEPLEWMLTPDSVGTFIDVGDDKQGALHRLVARNPVEKKTGSYALGRTSTVASLITRGNLRRGDDVPVKKGETWLSISSPSEGISRVTVMAPESDCWDQRKATATIYWVDAHWQFPAPLNLRAGEQAQLTTHVTRKEGELPASGWKVRYQVMNPEVALFDNGQSQPQAVIEAVVNENGDATAILRPIAPVAGTAFIQTTVIRPAGLDEALPRMTLGAGQTMVTWSAPRLVVRTGAPPFVARDEEFAIGINVSNSGDLTAENVRVLTELPPGVELVSTSLIQADGSRVPAQHTLVGAQILWDIDNLPAQTQLDIELNVRAKASFQIPVQARGAENTFAEDTVNVTVVQRNLVVTITPADPNARAEVGQETTFNIEVRNNGDQPISGVQVHAQGDQGLLAFAADTGQWQQHVVKVLEEPLLPNKPWTIQATYQVREPGQRCVQVTATGGNAQRATETACVNAVNPPPANPMVSARIVTGSQSVQQGEEVLVKYFVYNNGTVPLTDVRVVATYDPALTALQFTNGYESSQLGIFTVSWILPSIQPGEEQLVEGQFRVDGRPGVARLDVAVSSEQGANASADTTLQVLARTVAPPPATGPAVTPQPAQPPQQPTPQPPPIGAPPINGSTTPIPGPSTPPAQTPGAVGSGIGGLQVDIESRDNPVVVGDRISLDLVVTNNRNVPEDDVILSILLPAGTRLEAVQSTMFQGDPVENISADGIVRLQPISQLRAGEAIRYTVLITGNQPQLMTVRAEATSRQSPDGVGDETRLQVQAR
>NZ_CP036292.1|WP_145122708.1|5251703_5253005_-|twin-arginine-translocation-signal-domain-containing-protein
MQNDSTRRGFLKTSTIAATGAALTSSIARTAHAAGSDEIRFVVVGCGGRGTGAAMQIMNTKGNTKLVAVADAFGDKAERSIKSLANKHKDKVDVPKERIFTGLDAYKQAIDVDCDLVVIATPPGFKPQQFEYAVNKGRHIFMEKPVAVDAPGVRRVLKSVEESKKKNLMVGIGLQRRHEPQYIETIDRIHNGAIGDVIAQRVYWNGGGIWYRPKTEGQSEMAFQCNNWYHFNWVCGDQICEQHIHNLDVGCWVKGSYPVECNGMGGREMRMGGDATKSQIFDHTFCEYTFADGTKMFSQGRHLAGSWTHVGEAVHGSKGTADPSGSITGPNAWKFEGQRLNGHQQEQHDLIEALMAGEIYNEGEYGAKSTFTAILGREACYSGKVIKWDQLLAEGKDICPGIDEYTIDSVPPTVPGEDGKYPHPVPGKYNPFA
>NZ_CP036292.1|WP_145124246.1|5250426_5251272_-|SGNH/GDSL-hydrolase-family-protein
MLPIDRRGFSRSFAAIALFTAFLINPFPSNQAVAEHEGRVQILLLGDSTTEGSVPRRIRPEGPHLETVLEQLLAAEGDLPACDVINSSLSGEYIRRLFDSNRYDRDVAKLPGLDYIFIRYGINDRARLDNFVDDFPADFKKLIARLRVDHPDAVLIPMTVIPFSGEEASVQINDLIRGVAKEEQLEVFDIYPRYAAELEKGYNMLNYRRYALAKIPAKYHELVKPFVNGPSVEVMGNELDAILGHLPGWTRDRHPNLAGYNVIADETAKYLAPQLRKRSEK
>NZ_CP036292.1|WP_145122716.1|5269129_5270116_+|zinc-binding-dehydrogenase
MRAAVRHRYGPPEVLEICAIDRPECGPDQVLVRVHATTVNRTDCAVLMAKPFIMRPMTGWIHPKRATTGTDFAGEVVAVGAEVDEFEIGDRVWGFHDEGLSSHAEYLVAGRRENVAKMPAGVSFVDAAASLEAAHYAANFVKRLQVHQGDRVLVNGASGAIGSAVVQLLKNKGVIVTAVCGTANIPRVETLNPDEIIDYEREDFRQTSTRFHAVLDAVGKSSFGRCRHLLLPRGVYISSELGWGCQNPLLALVTPCLRGKVVRFPLPTNIAASMQQMGALLTEGKFAPLIDRQYPLEEIRDAFGYVLTGEKCGNVMLTFDVGVESLAD
>NZ_CP036292.1|WP_145122717.1|5270229_5272917_-|azurin
MRLSLLIIVLVSALSASAAEVKLEKGDHICLIGNELGERMQHHNYWESLLHQSFPEHELTVRNLCFPGDEPMDRIRSKNFGDPDSHLTHSKASVVMMFFGFNESFAGEEGLAEFTDQMTQLVNETKAKDYSGNGAPKIILVSPIAFEKTGDKNLPDGSQHNPRLEMYTAALADVAKQTEVGFVDLFHPSQKLFESHDERLTLNGSHLNEKGYQALAPAFVSAMGGSDAAEIKPELKAEVDDKNFHWWHRYRAVNGFSIYGDRGLAGQDGTRTYNNRDVMERERAILDQMTANRDARIWAIAQGRSVPAEVDDSNTLPFINVTTNVGGADDVNKKRGKLGSLDYHTAAEQQKMFELADGLQIELFASEEQFPELANPVSLQFDNKGRLWVSTMASYPHWQPKSKLDDKLLILEDVDNDGKADECKVFAGGLHQPTGFELGKGGAFIAQQPDILFAQDLDGDDAADTVIRKLAGFCSADSHHGISAFEWGPGGNLYFEEGTFKYSQVESPYGLNRLHEAGIWQYHPVTERFGVHVSVAFSNPWGHVFDRWGQNFIGDASPGFSYWAAPISGKIQYPMKHPGGSQHRRVANLETSGGTAGGDPKFALPTLYPKRTRPLGGCAMISSRHFPDEWQGNFLVTNCIGDRAVLNHKITEDGSGFVGVEVEKIVEGKDGNFRPVDLQIAPDGSLYVVDWHNALIGHLQHNLRDPSRDHSHGRIWRITHKTRPLVEPAKIAGQPIPALLDLLKLPEDRTRYRVRRELAERDPAEVVAAVNQWTENLDPSDADYEHHLTEALWVCQTHHAIQTELLDQVLNAKDHRARAAATRVVSFWADDLDSPIELLTPRINDEHPRVRLEAVRALSFLSGDEAAELALEVLNHDVDDALQYTLEETLRQLEQ
>NZ_CP036292.1|WP_145122718.1|5273061_5273829_-|leucine-rich-repeat-domain-containing-protein
MVQAYNPTRFSIPTWPAWAQMVVACFAGALAGGYISAKVAVSRSDESIRQQMEMRAIDRFVSLGGEVLRDGDKLSPVGMPALRGLGFYTIRSASDVRQAILYGGTLPGITQLHFAPFGVNRVGAGVTDGDVLRFANRNFKNVEYLDLSNCRIQDASVIQPMVDLKRLRLGNNPLTKNGVESLNLLDSVVELWIGWPDRTISPDSMYRSAELRKTLVKALTEMDKLQKVHLYDDIQLTQSEKAQLGELELVKAYMN
>NZ_CP036292.1|WP_145122719.1|5274162_5275125_+|hypothetical-protein
MGRTNRYEYKSLKEHYAQQRATESDFPRHNKSQLLLPRPSSSHAGVFGHEFSNDRPPGCRRFPDRFAADHGTSSTGISHPKRQSVCGTAAPESGPLFQGPSTTEDPTPGDLEKSAKMIQPKNSASDVDRFSSEAIEEALRRPVEAMFSDEPLENIIEILADKAGIPIRIDRRGLDDLGLTTDIPVTTAIKRASLEAALSIILSELDLTHTIANEHLVITSVEAAESQLITRIYWSGETGLQADRNAIDLITATVTPDTWEELGGPSVIRGIETESGSSSGLVVTTTHFTHRKLQQLLDMIAAGAKEKVIAMEMKSPGLTP
>NZ_CP036292.1|WP_145124248.1|5275121_5276081_-|flagellar-motor-switch-protein-FliG
MSLSTKAATIVMSRLTTAQVEAISLEIARMESVGGTEQEEVMHAFMGTKTSALNVSCGGLNLAKELIRQSMGTDADPVIQRIEQSIEQKPFAFVRRIEPRNLIQFVQDEHPQTIALILSHLPEGYCAEVLSGLDPEKQLEVIQRIAVVGSADTLAMADLERGLEMRLASLVNGTNLHVGGVEHVAGILNVSERSVERTIMEALAEEEPELVDEIRHLMFVFEDIAKMGDKDIQSLLKNVEASKWACALKGCSEPLVNKVMKNMSSRAADNLREEMGFLGAVRLSDVEAAQQGIVDMVRTLEDAGEIARPTGEEEEEFVS
>NZ_CP036292.1|WP_145122720.1|5276407_5277451_+|EamA-family-transporter
MLAPVQPSDRRRAIVALVLVNSMWGLSFPMMKCLNMQVDEHFSVTHLTASPMLRSSAAAWMIGIRFTAAMLLYLLFFHRTLRQVQMPHVLAGAAIGAMFVMGLILQVIGLGTIPASRSGFLTSLVVVVTPIISAIAQRRMPRPTVIAGAMLALFGVAVLAEVIQLRDGRIGFAADMRQTWTTGDWLTLLSVFFFSGQILLLDQLGKRYHSIAFTPSMFATTALLAFCTFAWLQFHVPESAVGGWTSLAVKPSFYLMLILLCSIPSLIAFAWMNKYQPMISAGQAAVIYTLEPVFASLWAMTLPAALSLCCTVAYANETFSTPLVIGGALVLAANALALWPQRRAGSR
>NZ_CP036292.1|WP_145122721.1|5277760_5278723_+|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase
MHANQPQAVEINTPAKLNLFLELLDRRADGFHELETVMVAINRFDRIRVALSDSDDVRVECGWLPHQAAVVERYRGSQAVATLPRSQDNLVTRALEQFRQRFSIADGFRASIAKTIPAGAGMGGASSDAAGALRAAAKLCQIDQHDQRLLQLAGELGSDIPFFFGSPQGSMSAAIATGRGERIDPVSIGGKLHFVVVHPPESVSTAEVYRRCQVPSRPSSAAAMLAALVGGRGTQIASQLLNRLSEPARATSEWIDRVLSAIARTPVLGYQVTGSGSACFGVCPNAAVASRIAHNLQAAGIGSAFAAHSVCIASPTRDMG
>NZ_CP036292.1|WP_145122722.1|5278756_5279323_+|stage-V-sporulation-protein-G
MDITEVRVKLMENSEDRLRAFCSITFDSCFVIRDLKIIDGTNGPFVAMPSRKLTGHCNRCGHKNYLRAPFCNQCGTKQRGGNGDNDGPQKLYADVAHPINSECREQIQRHVIEEFELELQRAQQPGYRSRYDDDFDSEDVAAAAAPQASELPAKLPPPAPHFHQRPSGEASSQRGGNDNDDSFGAGVF
>NZ_CP036292.1|WP_145122723.1|5279485_5279710_-|hypothetical-protein
MSDLPRMSIKSLRELIAKTELTLDELKTELHHREEAAQDSEIDHLEDHMKHAEISLQSIRDFFVILINECRSRH
>NZ_CP036292.1|WP_145122724.1|5279804_5280968_-|Na/Pi-cotransporter-family-protein
MRDRMDIAVPEEAAEAASNQSVWRQWLMVVCLVYLLICAVGLIGSGFKTATGSQAKQMFEFATNPFAGLVVGTVATALIQSSSTVTSIIVGLVAGGLPVSVAVPMVMGANIGTSITNTIVSLGHVREKKEFARAFSAATVHDFFNLLAVVIFLPLEMATGFLEKIGSGLAGIFVVGDASMGGLNFVKAATTPVVVFFKDGVAGMGTTAGGIVLILCGIVLIFLSIHFVGTLLKTLMVGKAKELLHSAIGKGPVSGICSGTLVTVLVQSSSTTTSLMVPLAGSGAFGLKQIYPFTLGANIGTCITALLAATAVDGNSAAALQIAFIHLTYNVLGVLFIFGVPMLRYLPVKAAEWLGETASENKLVALAYILSVFFVIPGMFLGVTSML

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Crispr_ID: NZ_CP036292_22

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_22

5447617-5447763

Orphan

Consensus_repeat	Method
GCCGCCCATGCCGCCGCC	CRT

3 spacers

The CRISPR arrays of NZ_CP036292_22

>merge|NZ_CP036292|22|5447617-5447763|CRT
AGCAAACATGCCGCCGCCGCCCATGCCGCCCATGCCGCCGCCCATGCCGCCGCCCATACCGCCGCCCATGCCGCCGCCCATACCGCCGCCCATGCCGCCACCGCCCATGCCGCCACCGAAGCCGCCGCCGCCGCCCATGCCGCCGCC

>NZ_CP036292|22|1|5447617-5447763|CRT
AGCAAACATGCCGCCGCC	GCCCATGCCGCCCATGCC
GCCGCCCATGCCGCCGCC	CATACCGCCGCCCATGCCGCCGCCCATACC
GCCGCCCATGCCGCCACC	GCCCATGCCGCCACCGAAGCCGCCGCC
GCCGCCCATGCCGCCGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145122827.1\|5439603_5439819_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145122834.1\|5457640_5458954_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|235589
NZ_CP036292.1\|WP_145122832.1\|5452240_5452594_-\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319911
NZ_CP036292.1\|WP_145124255.1\|5441915_5443232_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP036292.1\|WP_145122836.1\|5460222_5461368_-\|aminofutalosine-synthase-MqnE	unknown	unknown	gnl\|CDD\|213851
NZ_CP036292.1\|WP_145122837.1\|5462508_5463150_-\|UbiX-family-flavin-prenyltransferase	unknown	unknown	gnl\|CDD\|180312
NZ_CP036292.1\|WP_145122826.1\|5437309_5438668_+\|twin-arginine-translocation-signal-domain-containing-protein	unknown	unknown	gnl\|CDD\|223745
NZ_CP036292.1\|WP_145122838.1\|5463146_5463881_-\|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	unknown	unknown	gnl\|CDD\|234689
NZ_CP036292.1\|WP_145124254.1\|5439930_5440404_+\|SET-domain-containing-protein-lysine-N-methyltransferase	unknown	unknown	gnl\|CDD\|380929
NZ_CP036292.1\|WP_145122824.1\|5434893_5436150_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224094
NZ_CP036292.1\|WP_145124253.1\|5433955_5434882_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|181886
NZ_CP036292.1\|WP_145122829.1\|5443390_5444131_-\|dienelactone-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223489
NZ_CP036292.1\|WP_145124256.1\|5461579_5462500_-\|4-hydroxybenzoate-octaprenyltransferase	unknown	unknown	gnl\|CDD\|237247
NZ_CP036292.1\|WP_145122833.1\|5453829_5457528_+\|preprotein-translocase-subunit-SecA	unknown	unknown	gnl\|CDD\|237259
NZ_CP036292.1\|WP_145122835.1\|5459190_5460153_+\|Rpn-family-recombination-promoting-nuclease/putative-transposase	unknown	unknown	gnl\|CDD\|368098
NZ_CP036292.1\|WP_145122831.1\|5450660_5452130_+\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|369346
NZ_CP036292.1\|WP_145122828.1\|5440435_5441908_-\|response-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP036292.1\|WP_145122839.1\|5464047_5464476_+\|DUF393-domain-containing-protein	unknown	unknown	gnl\|CDD\|367833
NZ_CP036292.1\|WP_145122825.1\|5436146_5437127_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|223521
NZ_CP036292.1\|WP_145124252.1\|5433082_5433625_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377368

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145122834.1\|5457640_5458954_+\|glycosyltransferase	gnl\|CDD\|235589	PRK05749, PRK05749, 3-deoxy-D-manno-octulosonic-acid transferase; Reviewed.	1.26436e-146
NZ_CP036292.1\|WP_145122832.1\|5452240_5452594_-\|VOC-family-protein	gnl\|CDD\|319911	cd07247, SgaA_N_like, N-terminal domain of Streptomyces griseus SgaA and similar domains. SgaA suppresses the growth disturbances caused by high osmolarity and a high concentration of A-factor, a microbial hormone, during the early growth phase in Streptomyces griseus. A-factor (2-isocapryloyl-3R-hydroxymethyl-gamma-butyrolactone) controls morphological differentiation and secondary metabolism in Streptomyces griseus. It is a chemical signaling molecule that at a very low concentration acts as a switch for yellow pigment production, aerial mycelium formation, streptomycin production, and streptomycin resistance. The structure and amino acid sequence of SgaA are closely related to a group of antibiotics resistance proteins, including bleomycin resistance protein, mitomycin resistance protein, and fosfomycin resistance proteins. SgaA might also function as a streptomycin resistance protein.	4.08785e-34
NZ_CP036292.1\|WP_145124255.1\|5441915_5443232_-\|HAMP-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.08574e-28
NZ_CP036292.1\|WP_145122836.1\|5460222_5461368_-\|aminofutalosine-synthase-MqnE	gnl\|CDD\|213851	TIGR03700, mena_SCO4494, putative menaquinone biosynthesis radical SAM enzyme, SCO4494 family. Members of this protein family appear to be involved in menaquinone biosynthesis by an alternate pathway via futalosine, based on close phylogenetic correlation with known markers of the futalosine pathway, gene clustering in many organisms, and paralogy with the SCO4550 protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP036292.1\|WP_145122837.1\|5462508_5463150_-\|UbiX-family-flavin-prenyltransferase	gnl\|CDD\|180312	PRK05920, PRK05920, aromatic acid decarboxylase; Validated.	4.02879e-91
NZ_CP036292.1\|WP_145122826.1\|5437309_5438668_+\|twin-arginine-translocation-signal-domain-containing-protein	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	4.32023e-34
NZ_CP036292.1\|WP_145122838.1\|5463146_5463881_-\|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE	gnl\|CDD\|234689	PRK00216, ubiE, bifunctional demethylmenaquinone methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol methylase UbiE.	1.94023e-109
NZ_CP036292.1\|WP_145124254.1\|5439930_5440404_+\|SET-domain-containing-protein-lysine-N-methyltransferase	gnl\|CDD\|380929	cd10531, SET_SETD2-like, SET domain (including post-SET domain) found in SET domain-containing protein 2 (SETD2), nuclear SETD2 (NSD2), ASH1-like protein (ASH1L) and similar proteins. This family includes SET domain-containing protein 2 (SETD2), nuclear SETD2 (NSD2) and ASH1-like protein (ASH1L), which function as histone-lysine N-methyltransferases. SETD2 specifically trimethylates 'Lys-36' of histone H3 (H3K36me3) using demethylated 'Lys-36' (H3K36me2) as substrate. NSD2 shows histone H3 'Lys-27' (H3K27me) methyltransferase activity. ASH1L specifically methylates 'Lys-36' of histone H3 (H3K36me). The family also includes Arabidopsis thaliana ASH1-related protein 3 (ASHR3) and similar proteins.	6.21876e-17
NZ_CP036292.1\|WP_145122824.1\|5434893_5436150_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.03421e-89
NZ_CP036292.1\|WP_145124253.1\|5433955_5434882_+\|ABC-transporter-permease-subunit	gnl\|CDD\|181886	PRK09471, oppB, oligopeptide ABC transporter permease OppB.	5.51561e-107
NZ_CP036292.1\|WP_145122829.1\|5443390_5444131_-\|dienelactone-hydrolase-family-protein	gnl\|CDD\|223489	COG0412, COG0412, Dienelactone hydrolase and related enzymes [Secondary metabolites biosynthesis, transport, and catabolism].	5.40688e-40
NZ_CP036292.1\|WP_145124256.1\|5461579_5462500_-\|4-hydroxybenzoate-octaprenyltransferase	gnl\|CDD\|237247	PRK12886, ubiA, prenyltransferase; Reviewed.	6.19611e-79
NZ_CP036292.1\|WP_145122833.1\|5453829_5457528_+\|preprotein-translocase-subunit-SecA	gnl\|CDD\|237259	PRK12904, PRK12904, preprotein translocase subunit SecA; Reviewed.	0
NZ_CP036292.1\|WP_145122835.1\|5459190_5460153_+\|Rpn-family-recombination-promoting-nuclease/putative-transposase	gnl\|CDD\|368098	pfam04754, Transposase_31, Putative transposase, YhgA-like. This family of putative transposases includes the YhgA sequence from Escherichia coli and several prokaryotic homologs.	1.00148e-45
NZ_CP036292.1\|WP_145122831.1\|5450660_5452130_+\|DUF1501-domain-containing-protein	gnl\|CDD\|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	4.93161e-111
NZ_CP036292.1\|WP_145122828.1\|5440435_5441908_-\|response-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	1.58219e-176
NZ_CP036292.1\|WP_145122839.1\|5464047_5464476_+\|DUF393-domain-containing-protein	gnl\|CDD\|367833	pfam04134, DUF393, Protein of unknown function, DUF393. Members of this family have two highly conserved cysteine residues near their N-terminus. The function of these proteins is unknown.	7.64254e-25
NZ_CP036292.1\|WP_145122825.1\|5436146_5437127_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	0
NZ_CP036292.1\|WP_145124252.1\|5433082_5433625_-\|hypothetical-protein	gnl\|CDD\|377368	pfam04468, PSP1, PSP1 C-terminal conserved region. This region is present in both eukaryotes and eubacteria. The yeast PSP1 protein is involved in suppressing mutations in the DNA polymerase alpha subunit in yeast.	1.08884e-07

>NZ_CP036292.1|WP_145122829.1|5443390_5444131_-|dienelactone-hydrolase-family-protein
MRIEPTSHVDVQTPSGAMRTHLFRPAAEGKFPAVILYSEIYQMTAPIARTAALIAGHGFVVAVPDVYHEYTELGEAFAYDKEGTDRGNALKTTKELASYDADTRAVIDFLKSDPGCSGRIGAIGICLGGHLAFRAAMNPEVETGVCFYATDIHKGSLGKGMADDSLARIPEIHGELMMIWGRQDPHIPLEGRRIIYDALTAAETRFTWHEFNGEHAFMRDEGHRYDPALAMTLYAMVCQHLATQLK
>NZ_CP036292.1|WP_145124255.1|5441915_5443232_-|HAMP-domain-containing-protein
MAAVGVAAASYGLAERWATRDLQARWVGIQRTLSQSNFPLNSAVLRLLAELTQSELVTFASDGEVLQQTIDAPAATLVDLQQDLAASDSASEAAVVQTLKLPDRRYLAYRFETRNPSLRSDRVGSVLILFDESLLRDARRRAAILPLATGLSTIVALASITLVVTERMVRRIAALQRRVELVAAGDFESSVSDNNGDELGRLGAAVETMARQLKQLWATVHRQEGQKLLHQIAGGMAHQLRNSLTGARMAIELHADECGQSNDEGVQVAIGQIEQAEDYVRRLLMVASGRQDKDQPVDAMTCLQDVRTSLSPIARHLNVNVGWDLESQIATHRVKDGATLSAAVSNLVLNAMQTADDVQVLATIRNQQWLHVSVSDNGPGVAEEMIDQLFEPFVTSKPEGLGLGLPVVSRAAEHLDGRVVWMRRGDRTVFDFYARIVS
>NZ_CP036292.1|WP_145122828.1|5440435_5441908_-|response-regulator
MQKETETDAATKRQPDANSAVVLVVDDEPSICWAFEKMLTQQGHRVVTASSAEEGLRLAEEHSPAMVLLDVRLPNEDGISALPKFLAATDNAPVIVMTAFGDLDTAVSAIRRGASDYLIKPFRLADAQRTCRQALRAAADRRNQPATPQPMPSGQQVLVGQSPAMQQAFRQIALVAASDLSVLITGETGTGKELVAAAIHRNSQRADQPYIPIAPVALNPDLIESELFGHAKGAFTGATEDRAGLFEQAQGGTILLDEIGDLPLAAQVKLLRVLEQGEYSRVGDLRVRHANVRIIAATNCDLHQGVRQGTFREDLYYRLTGVQIHLPPLRQRPEDILLLCQHFLKAMDYPAIDAAIDAELLAELQSRPWAGNVRELKNAVQHAAVIARGRSLEATDFPPAKPASGEPPQSLAGSMAESVAAWATDAIADASEPLHDLHARFLAASEPALLRIAIEHTGGNRAKAAEMLGIHRGTLRDRLRAYNMDTSNGD
>NZ_CP036292.1|WP_145124254.1|5439930_5440404_+|SET-domain-containing-protein-lysine-N-methyltransferase
MNSETSPTTDCESDPAVNVQSTPIGKGVFADREFRAHDVIGWITGKIHDDPEYGSEYCIDIGGTATLEPDAPFRFLNHCCEPNSQFTWDELEEDSDAIPEVYLLALRDIEAGEQLTIDYNWAADCAIPCHCGAETCRGWIVTLDEIDQLPAKKQQAR
>NZ_CP036292.1|WP_145122827.1|5439603_5439819_+|hypothetical-protein
MLEVKGDPVTEPLENEEMEALRNQIWDFVYRAGNPQTINSIVDDLHLSDDSVREAVHHAWFVCEGDTVAIA
>NZ_CP036292.1|WP_145122826.1|5437309_5438668_+|twin-arginine-translocation-signal-domain-containing-protein
MSNQNRRDFLRTSAVAGASVSVPYFFSRSQTLADETKAKNDRIPIGLIGAGGMGMGNMRAAADYLDVVAIADADKSRQEAANKKLSNGKADVYDDYRKILERDDIKIVHVATPDHWHTKPVIEAMLAGKDIYCEKPLTLTIDEGKQIRKVQRETGRIVQVGTQQRSTFPLFTKAIAMVQQGRLGKILRVQAAIGGAPTSPAIPVAETPAGLDWERWLGPAPKTDYRFLADDKRGKTNGHYEFRWWYEYSGGKLTDWGAHHVDIATWALSVNGQPTSPVSIGGTASHPVEYKDGVPQQNDRYNTATAFNFVAKYADGTEMVIRNDTDNGVLIEGEKGRIFVNRRKLVGAPVEELKDNPLPEDAIQKAYKGLPMEENERKAHWANFLNCTQTRDEPISDVHSHMKMLNVCHLAGISARLGRTLNWDGENEQITGDSEANAMLARPYREGYEIEM
>NZ_CP036292.1|WP_145122825.1|5436146_5437127_+|ATP-binding-cassette-domain-containing-protein
MNKPLLSVENLGVGFGTDDGMLDAVRGVSFDVAAGETVGIVGESGSGKSVTNLAMMGLIPMPPGKITSGRAMFDNQDLLAMSQEQLSAVRGRRIAMIFQDPMTALNPFLTVEDQLTEVTRLHLGLNRRQATEHAIEMLTQVGISAPEKRLHDYPHQFSGGMRQRVMIAMALSCNPEILIADEPTTALDVTIQAQILDLLKKLQREHNTAIVMITHDLGVVANICHRVLVMYAGRIVERAPVDQLFANPQHPYTQGLLHSIPRWDQHGSELLKAIEGQPPHLAELPSGCAFHPRCPHKIDRCLSEDPRLENTSAERQKACFVDLNLS
>NZ_CP036292.1|WP_145122824.1|5434893_5436150_+|ABC-transporter-permease-subunit
MADPEIATEQMTDQQREHYRQLLADAQRIQGVSLWQDAWRRLRRRRASMLSLYFLIALAVLAFLTPALPLQSPLDKDLDNRRGMAPNLQSYRMGQRQDLQFTDNSLAAEVARVNESIATLQAERDSATDPEQREALTAKLEQLNTTAHPFSQMWNQLDPLAWQLTRLRVAIFGDWAVPSICGTDDLGRDMLARLFWGARVSLVVGVVATIVSLVIGVSYGATSGYFGGRVDSIMMRIVDVLYSVPFIFVVIFLMTFLSEESIAASLQSFGIDQITIFYIVIGAIYWLTMSRVVRGQVLSLKHEQFVDAARTVGASQQRIIFRHLVPNVLGIVIVYLTLTIPAVMLFEAFLSFLGLGVSPPDVSWGLLVNDGVQAITPLKSRWWLVVFPGSALAGTLFALNFLGDGLRDALDPRMKNQS
>NZ_CP036292.1|WP_145124253.1|5433955_5434882_+|ABC-transporter-permease-subunit
MQDLITFLIRRLGWMLLTLWIVFTVSFFLMRFVPGGPFSSEKNVPEAIKRNIEARYGLNDPLPTQYFRELGRDLTGDFGPSFRLEDFSVNEVIAQGFPISASLAILALSFALLLGVTAGVVSALKPGSLGDLTLMILATLGIAIPNFVLASILIIVFVFGLNLFPTAGWGSAWHLVLPALCLGAPVAAYIARLTRAGLLETIGQDYIRTAKAKGLPMYKVIGKHALRGALLPVVSYLGPAAARVLTGSIVLEQIFAIPGMGSHFVEAALQRDYSLAMGLVLVYTALLFLMNTLVDLSYSIIDPRVKLE
>NZ_CP036292.1|WP_145124252.1|5433082_5433625_-|hypothetical-protein
MSHYLVRTGAWGDISQHRPVDGGSYRRGDRVICETSRGLEIGEVVADVDAEASGGRILRRMTDQDELLQQRLERYKRKAVQECRDKLVAAKIDAVLLEVEQLFDGRTLYFHFLGETDSDVEAITNELADAYEQHVRSRHFAKLLREGCGPDCGTKEGGGCSGGCAVCVVASACSSTAKKS
>NZ_CP036292.1|WP_145122831.1|5450660_5452130_+|DUF1501-domain-containing-protein
MLSIKGAAGKDLCDPSLKRSRRDVLRIGGSGMLGLSLGSMLNLQAQASETPLGGGPGWGKAKSVILVYLQGGPSQLDLWDPKENVPDNVRSVFKPISTKIPGIQFTENLPRLAQLNDRFTMIRSMSYTPNGLFNHTAAIYQMMTGYTTDKVSPSGQLEPPSPKDFPNFGSNLIRLRPVDEPMLPFVMLPRPLQESNVVGKGGSAGFLGKSYDPYTLYPSGDDMDMEKMSRIKIDDLMLRPEVFSVRLQRRARLRDLINQQMPTINKAVESYELDEYYDRALSLIVSGRAREAFDLASEPVALRERYGQNTFGQSCLLARRLVEAGTRVVEVIWPKVANSDNHSWDQHSGLSKRMKDQSAPMFDAGFSSLIEDLDDRGLLDETLVVGVGEFGRSPQRGVSTSGNNNSADGRDHWPYCYTCVLAGAGIRRGYVHGKSDKTASAPLEDPVHPGELLASIYHSFAIHPETMVYNHLNQPRELVKAQAVTKLYS
>NZ_CP036292.1|WP_145122832.1|5452240_5452594_-|VOC-family-protein
MNRHEKINYVEFPSRDLAATKAFFTAAFGWTFVDYGPQYTAFSDQGLDGGFYQAELAANAELGSALIVFYSDSLEATQAKVEQAGGTVVKPIFSFPGGRRFQFTEPSGNELAVWSDK
>NZ_CP036292.1|WP_145122833.1|5453829_5457528_+|preprotein-translocase-subunit-SecA
MAILERIWELLGVIFGGLLGMVERGATAVFGSQNARQLKKLTARVEQINALEPKYQSMSDEELREQTQLFRNRLRAGETLDDILEEAFAVCREGGKRWLNMRHYDVQMIGGMVLHSGAIAEMVTGEGKTLVATLPCYLNALEGKGVHVITVNDYLARRDMEWMAPLYMGLGLTIGTIQGGMSTSARQAAYACDITYGTNNEFGFDYLRDNMRPAARGDDRFPKEMQQSQGPLNYAIIDEVDNILIDEARTPLIISGPAHTDPQKYAEANRIAKQLQKELHFTVNEKDHSVTLSDEGVREAEKLAGVESFYTAGNMEWPHLIDNSLKALHLYKRDVNYVVKDGQIVIVDEFTGRLMEGRQWSDGLHQSVEAKEGVRIKEETQTMATITLQNFFKLYNKLSGMTGTAMTEANEFWKIYHLDVVEIPTNRVLKRIENPDVIYMSEREKYEAVAQEIERAAKWDILEMKDGSEVWGTIQSENDSEISIIVKGEKNKQSVPREKIESIERSGRPVLVGTVSIEKSERLGSLLERRGIKHEVLNAKQHKREAEIVAQAGRLGAVTIATNMAGRGTDIILGGNPETMAWAQLQDKYPTRLEVPKEEWDALVGEIQEREKMKEAAEEVRTRGGLMVIGTERHESRRIDLQLRGRCGRQGDFGSSRFFLSLEDDLMRIFAGDWVKSVMVKLGMTEGEAIESAMVSRRIASAQKKVEERNFEIRKSLLEYDEVMDEQRKRVYTYRQQILDGVSCSELILSQIKGQVDHYVDILASEHYGAESFAAWSGSQLGCQLEPKDFRNMDYQAAEQYAKDQAERAAEAMVLEAVEENLPYEEDEADWNWNALVNWCNTKYGTNYRDKDLKQLERRELEEQLTDAGCKAIAKVDLSPGEMFLAADFGLQTIANWVRDKFGIEVTVDEMRDLESKDIKALLVQRAQQAYSVKEAEYPILAGLSRFCDNSGGQNRIDREGLALWAQDRFGVEVAVEDLRSLQRDELKQLLVDISSRSNDQAGSLHSDARKRVEDLFAGADAGTTATIAAGSDESLDALTQWMHEELRVRLPKDEIARMDRATMLRTVDGAVDERYHPEMRRMERQVLLNIVDTAWKDHLLAMDHLRSSVSLKSYAQMDPKVEYKREGMRLFETMWTSIGERTTDLIFRMESLNEDFVRSTFMGAQERHDDTPSGIDAGADQANEAASASQDGDAKIEPVRNRGEKIRPNDKCPCGSGKKYKACCKRHGTYA
>NZ_CP036292.1|WP_145122834.1|5457640_5458954_+|glycosyltransferase
MTYLLNIAYLLAAVAISPFLVWRSLRTGKYRAGWSAKLLGNVPHREGNQPCAWLHAVSVGEVNLLSNVVQRLQQSRPDMQIVISTTTATGMQLARTRFPEHTVFYCPLDFSWAVRRAFRRIRPDVLVLSELELWPNLIAITRQKGAEVVVINARLSERSFRGYRRFASLLRPTFRRLSLVLAQDETYARRFLQLGVDPSRVRVTGSIKFDGARTDRHAPEVVALRKLSAASKEQIVWIAGSTQAPEERIALDIYRRLADRFPQLRLILVPRHPERFKAVADQVVGAGLKLRRRSELQTPAESWPGDTVLLVDTVGELGCWWGLSDIAFVGGSMGSRGGQNMLEPAGFGAAVSFGPNTRNFRDIVAQLLAADAATVVRDRGALEQFVVNCVEDPAARRQQGRRAQVLVVGGQGAIDRTIAAVEQLLPAASPSSSRQAA
>NZ_CP036292.1|WP_145122835.1|5459190_5460153_+|Rpn-family-recombination-promoting-nuclease/putative-transposase
MGGDESLPNPHDRFIRHFLAEIDHVRELITWQLPAAVVDELDLTSIQPAKQSFVNKTLRENLSDLVFNVRLAHDAGEAMVVLLFEHKSAPDEMTPFQVLRYMVEISQERHRNGQPLCCVIPIIVYHGPQPWHVARSIQELIDVPAPLKPYIPQFSLPLIDLSQCSDEELRGKSIFLATMTLLKYIKRDELAEQLPGVLSLYRQLLPPATALESLEVVLRYLVNGTDRITREDLSTLVAKTLQHQGTSLMPTIAEQWLKEGMEQGIERGREQGELIGKIQAFQAVLGRETSQRDELTKLSTAELKRIVDELTSAIEENRSR
>NZ_CP036292.1|WP_145122836.1|5460222_5461368_-|aminofutalosine-synthase-MqnE
MIATEINARLRTIRDKVESQERLTMDDGLFLYQPDVPLHEVGELADLVRQRMNGNVAYYNINTHLNPTNVCVYRCRFCAFRADLRDPKGYAMDDEQVIARGQEATDNGCTEMHIVGGLHHQRPYEWYRGVLSTLSENFPKLHLKAWTPVEINWFEFQTKNSTEWVMNDMREAGLGSLPGGGAEIFHPEVRDQICEHKANTHAWFHTHRTAHQLGIRSNCTMLYGHIEKAYHRVDHLLRLRELQDETGGFQVFIPLAFHPENTKLSHLKKPSALDDLRNVAVSRLLLDNIQHIKAYWIMLGIGTAQTALSYGADDIDGTVRHELIYHDAGATTPEFLSVDRIRELIIEAGRVPVERNTIYQEVIRDPNDFSNWSIGETLPVS
>NZ_CP036292.1|WP_145124256.1|5461579_5462500_-|4-hydroxybenzoate-octaprenyltransferase
MAQPSKLRMMLEMIRFSHTIFALPFAALATVMAIKLPLPDGAAVRVRPLDLVAILICMVAARSVAMAFNRLADQAIDAGNPRTAGRHLPAGLLGRHEVTIFAILCAVGFLVGCALFLPNWLPLAASIPVLMFLCGYSLAKRFTAAAHLWLGVALSLAPICVWAALRGSAVLADPSDLLPPVILAAAVALWVTGFDIIYACQDEAFDRSEGLQSVPARFGAKGAFRIAAACHAGMVLVLLVLPSVVPALGLGWIYYAAVGSIAALLIYEHCLVRPDDLDRINQAFFQVNSIVSVGLLVAAGIDCWMG
>NZ_CP036292.1|WP_145122837.1|5462508_5463150_-|UbiX-family-flavin-prenyltransferase
MTRPLVVAITGGSGAVYAVRLLQVLLAGGREVFLMLSRSGADVIRQELKLELNLSVAGFDAEPLVTYRSPWSESVPELPDDWRERLTYEAIDDYFSPIASGSFLTDGMVVCPCSGSTLSSIARAASSNLVHRAAEVHLKERRSLVLVTRETPLSVIALENMTLAAKAGATLLPAMPGWYHGVRGLDDLVDFVVARILDQLGIENHLMQRWGEA
>NZ_CP036292.1|WP_145122838.1|5463146_5463881_-|bifunctional-demethylmenaquinone-methyltransferase/2-methoxy-6-polyprenyl-1,4-benzoquinol-methylase-UbiE
MATVDATNTKELDKSNARVREMFRQIAPRYDLMNHLLSLNIDKRWRNQTVSRLRIEGNAPILDVCTGTGDLALAISRRAGAETPVVGSDFCHAMLAIGDQKRKQQPEANVNFLEADAQHLPFDDNQFQVVTVAFGLRNVADTDRGLQEMVRVCRPGGQVVVLEFSQPTAPGLKQAYQFYFKHALPRIGQMLARNDKSAYQYLPESVGSFPCGQALANRMQQNGLHDVKFTPLTFGVATIYEGIK
>NZ_CP036292.1|WP_145122839.1|5464047_5464476_+|DUF393-domain-containing-protein
MFKSPDLADPDSRPDADVVIFDGQCNFCRGGVERLNWLDRRNRLAFISLHDERVAERYPDLSHDDLMQEMFVVDGQGKRHGGSDAVRYLSRQLALLWPIMPVLHLPGSAGVWRWMYKQVAKRRYRLAGKNCDSGSCKIHLNS

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Crispr_ID: NZ_CP036292_23

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_23

5862939-5863028

Orphan

Consensus_repeat	Method
TAAACCAAAAGGGGACAGGCACATTCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_23

>merge|NZ_CP036292|23|5862939-5863028|CRISPRCasFinder
TAAACCAAAAGGGGACAGGCACATTCCCAGACCGCCCGACACTGGCCGCAGGTCCGACAATTTAAACCAAAAAGGGGACAGGCACATTCC

>NZ_CP036292|23|22|5862939-5863028|CRISPRCasFinder
TAAACCAAAAGGGGACAGGCACATTCC	CAGACCGCCCGACACTGGCCGCAGGTCCGACAATTT
AAACCAAAAAGGGGACAGGCACATTCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123081.1\|5850498_5853552_+\|vitamin-B12-dependent-ribonucleotide-reductase	unknown	unknown	gnl\|CDD\|235828
NZ_CP036292.1\|WP_145123082.1\|5853676_5854174_+\|dihydrofolate-reductase	unknown	unknown	gnl\|CDD\|365932
NZ_CP036292.1\|WP_145117212.1\|5863727_5864612_+\|IS3-family-transposase	unknown	unknown	gnl\|CDD\|222853
NZ_CP036292.1\|WP_145124283.1\|5861129_5861501_-\|30S-ribosomal-protein-S13	unknown	unknown	gnl\|CDD\|235358
NZ_CP036292.1\|WP_145123083.1\|5854570_5855995_+\|TonB-dependent-receptor	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123090.1\|5865388_5866831_-\|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl\|CDD\|214624
NZ_CP036292.1\|WP_145123086.1\|5857818_5858595_-\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|369777
NZ_CP036292.1\|WP_145123084.1\|5856035_5857103_+\|potassium-channel-protein	unknown	unknown	gnl\|CDD\|367001
NZ_CP036292.1\|WP_145123094.1\|5870180_5871221_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381378
NZ_CP036292.1\|WP_145123093.1\|5869126_5870140_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379468
NZ_CP036292.1\|WP_145124284.1\|5874170_5874974_-\|succinate-dehydrogenase	unknown	unknown	gnl\|CDD\|239577
NZ_CP036292.1\|WP_145123087.1\|5858753_5859377_-\|50S-ribosomal-protein-L17	unknown	unknown	gnl\|CDD\|235522
NZ_CP036292.1\|WP_145123089.1\|5860560_5860944_-\|30S-ribosomal-protein-S11	unknown	unknown	gnl\|CDD\|180007
NZ_CP036292.1\|WP_145123085.1\|5857121_5857655_-\|RDD-family-protein	unknown	unknown	gnl\|CDD\|377640
NZ_CP036292.1\|WP_145123092.1\|5868414_5869047_+\|NADPH-dependent-F420-reductase	unknown	unknown	gnl\|CDD\|224996
NZ_CP036292.1\|WP_145117213.1\|5863425_5863731_+\|transposase	unknown	unknown	gnl\|CDD\|225511
NZ_CP036292.1\|WP_145123095.1\|5872127_5874101_-\|succinate-dehydrogenase-flavoprotein-subunit	unknown	unknown	gnl\|CDD\|236319
NZ_CP036292.1\|WP_145123088.1\|5859470_5860460_-\|DNA-directed-RNA-polymerase-subunit-alpha	unknown	unknown	gnl\|CDD\|235359
NZ_CP036292.1\|WP_145100442.1\|5871242_5872088_-\|succinate-dehydrogenase-iron-sulfur-subunit	unknown	unknown	gnl\|CDD\|181515
NZ_CP036292.1\|WP_145123091.1\|5867308_5868310_-\|TIGR00730-family-Rossman-fold-protein	unknown	unknown	gnl\|CDD\|224527

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123081.1\|5850498_5853552_+\|vitamin-B12-dependent-ribonucleotide-reductase	gnl\|CDD\|235828	PRK06556, PRK06556, vitamin B12-dependent ribonucleotide reductase; Validated.	0
NZ_CP036292.1\|WP_145123082.1\|5853676_5854174_+\|dihydrofolate-reductase	gnl\|CDD\|365932	pfam00186, DHFR_1, Dihydrofolate reductase.	3.13383e-59
NZ_CP036292.1\|WP_145117212.1\|5863727_5864612_+\|IS3-family-transposase	gnl\|CDD\|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	7.3877e-74
NZ_CP036292.1\|WP_145124283.1\|5861129_5861501_-\|30S-ribosomal-protein-S13	gnl\|CDD\|235358	PRK05179, rpsM, 30S ribosomal protein S13; Validated.	1.26622e-62
NZ_CP036292.1\|WP_145123090.1\|5865388_5866831_-\|SpoIIE-family-protein-phosphatase	gnl\|CDD\|214624	smart00331, PP2C_SIG, Sigma factor PP2C-like phosphatases.	2.0647e-19
NZ_CP036292.1\|WP_145123086.1\|5857818_5858595_-\|methyltransferase-domain-containing-protein	gnl\|CDD\|369777	pfam08241, Methyltransf_11, Methyltransferase domain. Members of this family are SAM dependent methyltransferases.	8.00824e-16
NZ_CP036292.1\|WP_145123084.1\|5856035_5857103_+\|potassium-channel-protein	gnl\|CDD\|367001	pfam02254, TrkA_N, TrkA-N domain. This domain is found in a wide variety of proteins. These protein include potassium channels, phosphoesterases, and various other transporters. This domain binds to NAD.	1.26119e-28
NZ_CP036292.1\|WP_145123094.1\|5870180_5871221_-\|aldo/keto-reductase	gnl\|CDD\|381378	cd19152, AKR_AKR15A, AKR15A family of aldo-keto reductase. The AKR15 family includes Microbacterium luteolum pyridoxal 4-dehydrogenase (PLD), Pseudomonas sp. D-threo-aldose 1-dehydrogenase (FDH), and similar proteins. PLD (EC1.1.1.107) catalyzes irreversible oxidation of pyridoxal. FDH(EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose. FDH (EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose.	2.97789e-106
NZ_CP036292.1\|WP_145123093.1\|5869126_5870140_+\|hypothetical-protein	gnl\|CDD\|379468	pfam14100, PmoA, Methane oxygenase PmoA. This family is a putative methane oxygenase.	2.21906e-55
NZ_CP036292.1\|WP_145124284.1\|5874170_5874974_-\|succinate-dehydrogenase	gnl\|CDD\|239577	cd03497, SQR_TypeB_1_TM, Succinate:quinone oxidoreductase (SQR) Type B subfamily 1, transmembrane subunit; composed of proteins similar to Bacillus subtilis SQR. SQR catalyzes the oxidation of succinate to fumarate coupled to the reduction of quinone to quinol. Bacillus subtilis SQR reduces low potential quinones such as menaquinone. SQR is also called succinate dehydrogenase (Sdh) or Complex II and is part of the citric acid cycle and the aerobic respiratory chain. SQR is composed of a flavoprotein catalytic subunit, an iron-sulfur protein and one or two hydrophobic transmembrane subunits. Members of this subfamily are classified as Type B as they contain one transmembrane subunit and two heme groups. The heme and quinone binding sites reside on the transmembrane subunit. The transmembrane subunit of Bacillus subtilis SQR is also called Sdh cytochrome b558 subunit. The structural arrangement allows efficient electron transfer between the catalytic subunit, through iron-sulfur centers, and the transmembrane subunit containing the electron acceptor (quinone). The reversible reduction of quinone is an essential feature of respiration, allowing transfer of electrons between respiratory complexes.	9.82785e-74
NZ_CP036292.1\|WP_145123087.1\|5858753_5859377_-\|50S-ribosomal-protein-L17	gnl\|CDD\|235522	PRK05591, rplQ, 50S ribosomal protein L17; Validated.	1.83353e-35
NZ_CP036292.1\|WP_145123089.1\|5860560_5860944_-\|30S-ribosomal-protein-S11	gnl\|CDD\|180007	PRK05309, PRK05309, 30S ribosomal protein S11; Validated.	1.3401e-81
NZ_CP036292.1\|WP_145123085.1\|5857121_5857655_-\|RDD-family-protein	gnl\|CDD\|377640	pfam06271, RDD, RDD family. This family of proteins contain three highly conserved amino acids: one arginine and two aspartates, hence the name of RDD family. This region contains two predicted transmembrane regions. The arginine occurs at the N-terminus of the first helix and the first aspartate occurs in the middle of this helix. The molecular function of this region is unknown. However this region may be involved in transport of an as yet unknown set of ligands (Bateman A pers. obs.).	9.27229e-13
NZ_CP036292.1\|WP_145123092.1\|5868414_5869047_+\|NADPH-dependent-F420-reductase	gnl\|CDD\|224996	COG2085, COG2085, Predicted dinucleotide-binding enzymes [General function prediction only].	2.20807e-46
NZ_CP036292.1\|WP_145117213.1\|5863425_5863731_+\|transposase	gnl\|CDD\|225511	COG2963, COG2963, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	8.08038e-08
NZ_CP036292.1\|WP_145123095.1\|5872127_5874101_-\|succinate-dehydrogenase-flavoprotein-subunit	gnl\|CDD\|236319	PRK08641, sdhA, succinate dehydrogenase flavoprotein subunit; Reviewed.	0
NZ_CP036292.1\|WP_145123088.1\|5859470_5860460_-\|DNA-directed-RNA-polymerase-subunit-alpha	gnl\|CDD\|235359	PRK05182, PRK05182, DNA-directed RNA polymerase subunit alpha; Provisional.	7.74451e-154
NZ_CP036292.1\|WP_145100442.1\|5871242_5872088_-\|succinate-dehydrogenase-iron-sulfur-subunit	gnl\|CDD\|181515	PRK08640, sdhB, succinate dehydrogenase iron-sulfur subunit; Reviewed.	2.9521e-144
NZ_CP036292.1\|WP_145123091.1\|5867308_5868310_-\|TIGR00730-family-Rossman-fold-protein	gnl\|CDD\|224527	COG1611, COG1611, Predicted Rossmann fold nucleotide-binding protein [General function prediction only].	3.1799e-49

>NZ_CP036292.1|WP_145124283.1|5861129_5861501_-|30S-ribosomal-protein-S13
MGVDVPNDKQIQYSLTYLYGVGLHTAREACERLQIDPKRKAFDLSEEEVSKLAAFLESEYTVEGPLRRQLSSNISRLREVKSYRGIRHRLGLPVRGQRTKTNARTRKGPKKTVAGKKGVKDLR
>NZ_CP036292.1|WP_145123089.1|5860560_5860944_-|30S-ribosomal-protein-S11
MSKVKTKKKQRRNVVSGVAHIHATFNNTTVTITDPKGETLCWASAGTCGFKGSRKSTPFAGQMAAQQCAEKAQKFGVREVEVRVKGPGSGRENAITSLQSAGLKVKLIEDVTPIPHNGCRPRKKRRV
>NZ_CP036292.1|WP_145123088.1|5859470_5860460_-|DNA-directed-RNA-polymerase-subunit-alpha
MHIRWRGMELPSTVEVDRESLSPTYGKFVAEPFERGFGNSVGNSLRRVLLSSLEGSAVTQIKVHGAQHEFSSIAGVMEDVTEIVLNVKSLIVRNHSESTRVITVQRNTAGDVTGNDVQTDQDVEIINNNHVLATLTEDVPFMMEMVVENGRGYVPSTEHSTGEHEIGIIPIDAVFSPVTRVRYEVEETRVGQKTNYDRLIMEIWTDGTVGPELALTESAKIMRKHLNPFVQYTELGPGIHTVARGGANSAEAQLEAKLNMPISDLRLSVRAGNCLESEQIRTVRDLVVRTEDQLIEVRNFGDTTLNEVRDKLNALGLHLGMRVPTGGLM
>NZ_CP036292.1|WP_145123087.1|5858753_5859377_-|50S-ribosomal-protein-L17
MRHRRKGRVLGRSPSHRKAMYKNLASSLFLTERDAEFDDNAPKVKGRVVTTLEKAKEIRPLVERCITIAKRSLAAEEESQKYATDAERGSEAWKTWRKSENWRKWSDARAPAIAARRRVLQLLGDKQAMRIVFDEMADRFRDRPGGYTRIMRLATPRLGDAGTRAILEFVGVNDRVSQKAERPSFDDDSDSAADDEVATEEETAAKE
>NZ_CP036292.1|WP_145123086.1|5857818_5858595_-|methyltransferase-domain-containing-protein
MDVRSYNRTAWNRKVEQADRWTQPAGSEVIDAARGGDFRIVLTPTKPVPMAWFPPLHATQTLCLASAGGQQAPVLGAAGARVTVFDNSPRQLDQDRLVAERDGLDMSFEEGDMADLSRFSDESFDLIFHPCSNGFIPNVIPVWRECFRVLRSGGVLLAGFTNAVRYIFDDERRLNGNLEVRYSLPYSDLDHRNEPHIRKEIELGNPLEFGHTLEDQIGGQLNAGFMLTGFYEDRFGESDDDPLSSFLDTFIATRAVKP
>NZ_CP036292.1|WP_145123085.1|5857121_5857655_-|RDD-family-protein
MIDPGVRTMSDNPYASPVATPAAIPTADDGASIDGVPFASQNRRLVNFLVDNVMVQIVAGGVAGVIGEAFVETSSGQITQDEVATLQLMGMVVGLGVVVFYFVLLEATLGVTIGKLLTGTRVVDAGGGKASFGKIVGRTFARLIPFEPLSFLFGDKTTGWHDSLSGTRVVHTRAARR
>NZ_CP036292.1|WP_145123084.1|5856035_5857103_+|potassium-channel-protein
MGDSTSMRKMLVGLTFLSITCVAAVLGFIAAGWSVVDSIYMVVITIFGVGYGEVHPIDSTGMKVFTAFIIIAGCSSGIYVVGGFVQMVAEGEFYRALGARRMSQGIEQTSNHVIICGFGRVGRNLAEELRSLDQPFVCIDEKPDRIVQAEELGYLVVTGNAGEEETLIKAGIHRAAYLATVLPEDAANVFITLTARELTQELQIIARGESESTQRKLVRSGANHVVMPEAIGAARIANMLSCPTADSLISDASQRNRWNNDLKALRLAIREVRAEGASAVAGGKIADLNLHDGRPLIVAILSTDGRIRRNPDTNEPILPGDILYVMSSQEKTLAVIRQVQAQRAELTYRGSRVQS
>NZ_CP036292.1|WP_145123083.1|5854570_5855995_+|TonB-dependent-receptor
MHLSPRIPTSEPIDTHQKALQVNLDPRRYGTFAEIGAGQEVVRWFFRVGGGAGTIAKSMSAYDMKVSDAIYGRASRYVCRERLQAMLDYEHKLNLDRLKDVRGDTTAFFAFADTVSARNFQGTNDCHGWIGVKFQAHPRDDDSQIIIHVRMLDNEAALQQEALGIVGVNLVHGAFALNHEPELLVDSLLDGLSTSRIEIDMIEFSGIAFRHVDNRLMSLKLVELGLTGAAMFAANGDVLQPSEFFHRKPILVERGSFRPVCNVNLDMLHCAHEKFTQLPSVQGKEVAQVMEITMRNLKAEGEIDLRDFLARADVMSACGMTVLISDYFQYYRLASYLSRYTKESIAITMGAASLLDLFDEKYYAGLEGGILESFGRLFKNDLKIYCYPLRDQTTGEMTTCENLEIKPELQKLYGYLKDRGGINDLDNFNSDCLNIFSRDVLCKIKQGDMSWESMVPPPVADVIKSRSYFEYQAT
>NZ_CP036292.1|WP_145123082.1|5853676_5854174_+|dihydrofolate-reductase
MLETDRVSLTAVVAATPTGTIGLDNDMPWQLSHDLRRFKRLTMGSILIMGRKTFDSIGRPLPGRTTFVLTRDQSWAHPGVEAFTDPDAMLVAVGDRSAYVVGGAQIYTAMMPACDHLYLTRVWSQVVGDTAVEIDLQDWRCRFVERIPAGSRDSIPSEFSVWDRA
>NZ_CP036292.1|WP_145123081.1|5850498_5853552_+|vitamin-B12-dependent-ribonucleotide-reductase
MAIAPTCPQNDLQHGIDHARAKFSSAGRSSVVGLKIDSEFCPTDVDSPFDTSEWVLRSAAIKDETGTALFEQHACEVPAKWSQLATNVVVSKYFYGDPKKAERETSVRQLIHRVTRTISDWGLADGYFDTAEDGENFYRDLTWLCLHQHGAFNSPVWFNVGLYDQYGVTGAKCNWHYDKTQGRVDQPENPYEFPQGSACFIQKVEDNMEDIMRLATSEAMLFKFGSGTGTDLSSIRSERENLSGGGNPSGPLSFMRVYDQIAAVVKSGGKTRRAAKMQSLKVWHPDILEFIECKWSEERKAHALIQQGYDSNFNGEAYSSVMFQNANLSVRVTDDYMKAVRDGKRWQTQWISEKATGTPPEYDARELLNKMAECAWHCGDPGVQYDSTINTWHTCPNSGRINASNPCSEYMFLDDTACNLASINLMKFRRADGSFDVDRFHAACRVFFIAQEILVDHASYPTADIALNSHNYRPLGLGYSNLGSLVMTSGLPYDSDGARGLCGSLTALMHGSANLTSAEMAGVVGPFEGFANNREPMLKVMGMHRDAVEDINDEGPEYLKDAARNLWDKVIELGNRYGFRNAQATVLAPTGTISFLMDCDTTGVEPDIALVKYKQLAGGGMLKIVNRGVEGALESLGYDTTQAKEIVAYIDEHDTIEGAPHLADEHLPVFDCAFTPAGGTRSIAWQAHVTMMAAAQPFLSGAISKTVNMPTDSTPQDIADAYFWGWELGLKAIAIYRDGSKQSQPLNTKSGEKTAADAEVKVVEKVVYRPRRERLEDTRHSLTHKFNIAGHEGYINVGLYPDGRPGEVFITMAKEGSTIGGLMDSFGTSTSIALQYGVPIEVLVNKFTHTRFEPMGHTSNPDIRIAKSIVDYIFRWMGITFLAGYREATVPGAAEKSDSGTSTETKSPASEAASKESGDGEEMKLGGNGPTTETHDTAARFTVGNLPTVNIDALERAGVSMQISADGANDIDKPGSRSDQFARFQSDAPACDNCGSITVRNGNCYLCHNCGASMGCS
>NZ_CP036292.1|WP_145117213.1|5863425_5863731_+|transposase
MPENPRQPRRVHSDEFKRSAVELVTKKGYTIKQAADAVAVAPRSIRDWIKKFDASAIPASVGSSNDALIAENRRLKKALLQAEMERDILKKATAYFAKESK
>NZ_CP036292.1|WP_145117212.1|5863727_5864612_+|IS3-family-transposase
MKYAWIKQHRDSFPIQTMCRVMRVSRSGYYAWCVREPSARKQRTNKIRADVQRVHASSKQIYGSYKVAELMQADAQLESASRNTVAKAMREMGLKSKVHKRFTPTTTVADPTKVPAPNLLDQVFEAEGPNRKWVTDITYLPSANGWIYLAVVLDLFSRKVVGWSISESLATPLVEDALRQAIANRRPDTANLLHHSDRGCQYTSSEYQRTLKTLGITCSMSRTGCCYDNAVMERFFWSLKHEWTKFESFADINDARSSVFEYIEAFYNSTRIHQTLGYRTPNQFEVDHEQSLAL
>NZ_CP036292.1|WP_145123090.1|5865388_5866831_-|SpoIIE-family-protein-phosphatase
MSAFWQAYVDATGWRIKPSTGTTAHRLMLLPACTEAMMDVDSADAQPAVSKSAAETLAQAASRIADRLREFEGLLRNQEATHAVEDANAGCLPAAGHIADRLEAVLKEASAATGCDAAGLYLLDADTSHLKLRSCFGLPKSRLAQPPRALRGALGDLEALVSPVVTIEDIPRMPHWESPEERGAAIVVAIRGGDLPLGTLWLWDDQPRDITSAQQASATLAAGRIAAELEREVIGTKAAEQAEVRDELRAAAAWQSRQLPPAVPLDKDWDVAGWNEAAEAVGGDWFAWDILPDGKIAIAIASVGASGIESALTAATARSAWQSHTGYRHKTNQVLSRVNDTLWQTSTGDQSTSLLYVTVDPETGEGQFSSAGTCQGLIVNRYGYRMLASPTEPLGRDPDVRPLVHTMRLLPGEALVLVSQGAIASNGAPESGRLTQQTLTDSIRHELVNGPEPALSCLRRLFAQAGPAAADRSIAILQRQ
>NZ_CP036292.1|WP_145123091.1|5867308_5868310_-|TIGR00730-family-Rossman-fold-protein
MTEKPDDSGSNKETRLRSPDLIEVMRKTIDRLVRDRTARGDLKILSRTLIELRYAFSVFRPYRRHRKVTVFGSARTAPSHPTFKAAEEFGRRMAAEDWMVVTGAGSGIMEAGHRGAGREHSMGLNIMLPFEQGANPVIEGDRKLVTMKYFFTRKLMFVKECHAVVSLPGGFGTLDETAEVLTLLQTGKHPMIPVVLLDAPGGTYWKEFGKFVDSQLLDGGMISPEDLRLYKITESVDEAVAELDRFYRVYHSMRYVNGKLVLRLQRPLGAAKLAAVNDRFSDIVVKGGFEQMAALPEEHSEAEIAELPRLVFLFNRRAMGRLRMLIDFINEDE
>NZ_CP036292.1|WP_145123092.1|5868414_5869047_+|NADPH-dependent-F420-reductase
MDIAVLGTGNVGATLGRRLAGLGHNIVFGSRLPQSERVQQLIEENPHAHAAETIAEAARQCDTILFAAPWTAARETLTNAGDLTGKTLIDCTNPLNETFDGITLGHTESAAEKIAHWAAGAHVVKAFNTASLATMENPDFDGQRATMFYCGDDITAKATAGTLIDELGFEAIDAGDLQSARYLEPMAMLYIQLAIHQKMGSQFALKMLRR
>NZ_CP036292.1|WP_145123093.1|5869126_5870140_+|hypothetical-protein
MTLTTRSLLSSLLAAWCLLASPIAAADLQVKETNAAIEIASDGKSVLVYNKQSPPVPDGIDPIYHRSGFLHPVASPAGNVVTAAFPADHPHQQGVFSAWVRTNYDGREIDFWNLAGGVGRVSHERVVKTFTENESAGFEVDLIHHTVAEPKVDILRERWRITVQPTDGSYRCFDLQTTQEALTDKPLTVEKYHYGGVATRGPARWSLPSGKKAAAKASDADNNKPSEPISEIVDEHGHDRIAGNHHPTRWVTLSGTEGDDLVCITMLGHADNFRAPQPARLHPSMPYFCFAPCVTGEFQIAKDQPYEASFRFLVTDGKPDPAWIEQQWQAWCGDKAQ
>NZ_CP036292.1|WP_145123094.1|5870180_5871221_-|aldo/keto-reductase
MQRQLFGKTGLRIPPVVFGSTSLGNLFAEVPDEAKQQVVAEWFRRVEAPVFIDSAGKYGAGMSLEIIGRELSRLNIDPADVVISNKLAWTRQPLVGDEPTFEPGAWFGLTHDARQEISYEGILRCYHQGNELLGDYQAGLVSVHDPDEYLAAATDPADHKQRWHDIEEAYRALGELRSEGKVLGVGVGAKDWTSIRDVCDRVDLDWVMLANSLTIMKHPPELLAFIEQLDEAGVGILNAAVFNAGFALGGKFYDYRVVTGESAEDRELLDWRQRFQTACQRFDVAPAAACLEFARSVPGIQAVAISSSSPHNIARTVAAVDGAAPPSFWSHLKEMHVIDPSFPFLG
>NZ_CP036292.1|WP_145100442.1|5871242_5872088_-|succinate-dehydrogenase-iron-sulfur-subunit
MIAPEKSMPDTIDVRILRQEGPGKKPYWERHRIQYEREMNVISVLQKVAAQAKTVEGKDVAPVAWDCGCLEEVCGSCTMVINGRVRQSCSALVDKLLADQPSHIELAPMTKFPVLRDLLVDRSRLFRGLKKIKAWVPVDGYYDMGPGERQSREQQEQAYPLSQCMSCGCCLDACPQYKKIEVDRITGESEEDYQARCNAEYDNAFIGANAISQVMLFNDHPVGKMMADERMEALTEPGGIQVCGNAQNCVAVCPKEIPLTTSIARAGRAATVHAIKQFFDR
>NZ_CP036292.1|WP_145123095.1|5872127_5874101_-|succinate-dehydrogenase-flavoprotein-subunit
MSQQRVVVIGGGLAGLSATMKLAELGIPVDLISLTPVKRSHSVCAQGGINACNDQTRQLGDSEWKHFDDTVYGGDFLQHQPPVKEMTLWAPKVIELMDRLGVPFNRTGEGFIDRRRFGGTLYKRTAFSGATTGQQLLYALDEQVRRRESEGLVRKFEFWDFLGPIQDSNGECRGVVAQDMVSMEIRGFPASAVVVASGGCGLLYGRSTMSVFCNGSAASRCFQAGAKYGNAEFIQVHPTAIPGADKLRLMSESARGEGGRVWVPKKPQDPRSPRQIPENERYYFLEERYPEYGNLVPRDIATREIFDVCVNDGLSVEAGRMCVYLDLTHIERSELDRKLGGILEIYEKFQGVDPRDEPMKIFPAVHYSMGGLWADYVRSADGGMEAGNPRNQMTTINGLYAMGECDYHYHGANRLGANSLLSCIFTGLFSGPGIANFIQGRSEATTSDVEAAVRKQQERHDALLNQSAGGENPYLIHQELGDVLTRAATVVRKNEQLEEAIKTVDDLHQRVQKVSLSDTGTWTNQNVIFAKAVQDMFPLAKALLKGALQRDECRGAHFKPAFSMPELTSDNDADRRREAEAWCDRFEENNKKFLKSSVATWEGNDVSIAYEDVDTSLIPPRPRLYGLKGAEVISEVWNERAAKAKAAAATASQDAAN
>NZ_CP036292.1|WP_145124284.1|5874170_5874974_-|succinate-dehydrogenase
MCVHLTTNASLMAGPGAFQRMVNQIHSLGPALPVVEWGFIFLPLLFHAIIGIWIGMTGESNTDRYKYTANRRYRFQRITGYIAFVYITMHVFHLHGWFHFGPWLDYIATPLGMAQFKPYNAASSLAHAMDGVFWPAFYLVGVLSCVYHFANGLWTAGITWGLWVSPAAQKRASMLCGGIGLLVGIISITAWVGALTVDPKEARIVEDRMYEAGLESGAVFDDPHKRSAPEAVESEESEAEVDADASTADEAAASDEKTAEPETSAAE

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Crispr_ID: NZ_CP036292_24

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_24

5919397-5919491

Orphan

Consensus_repeat	Method
AAGAACGTATCGGCCTGGCATAA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_24

>merge|NZ_CP036292|24|5919397-5919491|CRISPRCasFinder
AAGAACGTATCGGCCTGGCATAAGTAGAACGCGCCCGAAGCCCCACTTGGATCAAGCGCGTAATGGATCCGAAGGAACGTATCGGCCTGGCATAA

>NZ_CP036292|24|23|5919397-5919491|CRISPRCasFinder
AAGAACGTATCGGCCTGGCATAA	GTAGAACGCGCCCGAAGCCCCACTTGGATCAAGCGCGTAATGGATCCGA
AGGAACGTATCGGCCTGGCATAA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123124.1\|5922759_5923902_+\|5-(carboxyamino)imidazole-ribonucleotide-synthase	unknown	unknown	gnl\|CDD\|235674
NZ_CP036292.1\|WP_145123118.1\|5913304_5914795_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145123125.1\|5924004_5924919_+\|polyphosphate-kinase-2	unknown	unknown	gnl\|CDD\|213852
NZ_CP036292.1\|WP_145123128.1\|5927048_5927504_-\|DUF1569-domain-containing-protein	unknown	unknown	gnl\|CDD\|369441
NZ_CP036292.1\|WP_145123123.1\|5922241_5922763_+\|5-(carboxyamino)imidazole-ribonucleotide-mutase	unknown	unknown	gnl\|CDD\|376377
NZ_CP036292.1\|WP_145123116.1\|5910829_5911750_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123113.1\|5905714_5906812_-\|DUF1611-domain-containing-protein	unknown	unknown	gnl\|CDD\|225902
NZ_CP036292.1\|WP_145123127.1\|5926140_5926452_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123129.1\|5927652_5931015_-\|helicase-SNF2	unknown	unknown	gnl\|CDD\|223627
NZ_CP036292.1\|WP_145124287.1\|5919509_5920430_-\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP036292.1\|WP_145123115.1\|5908289_5910368_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|378963
NZ_CP036292.1\|WP_145123120.1\|5915511_5918226_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123117.1\|5912026_5913226_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123111.1\|5901997_5904661_+\|DUF11-domain-containing-protein	unknown	unknown	gnl\|CDD\|375050
NZ_CP036292.1\|WP_145123130.1\|5931113_5935208_+\|ATP-dependent-RNA-helicase-HrpA	unknown	unknown	gnl\|CDD\|273900
NZ_CP036292.1\|WP_145123112.1\|5904686_5905718_-\|dipeptide-epimerase	unknown	unknown	gnl\|CDD\|239435
NZ_CP036292.1\|WP_145123114.1\|5907056_5908250_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|380485
NZ_CP036292.1\|WP_145123122.1\|5920759_5922019_+\|LL-diaminopimelate-aminotransferase	unknown	unknown	gnl\|CDD\|235772
NZ_CP036292.1\|WP_145123119.1\|5914903_5915194_-\|transcriptional-regulator	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123126.1\|5925008_5926064_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123124.1\|5922759_5923902_+\|5-(carboxyamino)imidazole-ribonucleotide-synthase	gnl\|CDD\|235674	PRK06019, PRK06019, phosphoribosylaminoimidazole carboxylase ATPase subunit; Reviewed.	1.4295e-177
NZ_CP036292.1\|WP_145123118.1\|5913304_5914795_-\|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.	1.34426e-69
NZ_CP036292.1\|WP_145123130.1\|5931113_5935208_+\|ATP-dependent-RNA-helicase-HrpA	gnl\|CDD\|273900	TIGR01967, ATP-dependent_RNA_helicase_HrpA, RNA helicase HrpA. This model represents HrpA, one of two related but uncharacterized DEAH-box ATP-dependent helicases in many Proteobacteria and a few high-GC Gram-positive bacteria. HrpA is about 1300 amino acids long, while its paralog HrpB, also uncharacterized, is about 800 amino acids long. Related characterized eukarotic proteins are RNA helicases associated with pre-mRNA processing. The HrpA/B homolog from Borrelia is 500 amino acids shorter but appears to be derived from HrpA rather than HrpB. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP036292.1\|WP_145123128.1\|5927048_5927504_-\|DUF1569-domain-containing-protein	gnl\|CDD\|369441	pfam07606, DUF1569, Protein of unknown function (DUF1569). A family of hypothetical proteins identified in Rhodopirellula baltica.	1.62336e-39
NZ_CP036292.1\|WP_145123123.1\|5922241_5922763_+\|5-(carboxyamino)imidazole-ribonucleotide-mutase	gnl\|CDD\|376377	pfam00731, AIRC, AIR carboxylase. Members of this family catalyze the decarboxylation of 1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (AIR). This family catalyze the sixth step of de novo purine biosynthesis. Some members of this family contain two copies of this domain.	1.06057e-83
NZ_CP036292.1\|WP_145123113.1\|5905714_5906812_-\|DUF1611-domain-containing-protein	gnl\|CDD\|225902	COG3367, COG3367, Uncharacterized conserved protein [Function unknown].	2.1326e-81
NZ_CP036292.1\|WP_145123129.1\|5927652_5931015_-\|helicase-SNF2	gnl\|CDD\|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	5.70611e-114
NZ_CP036292.1\|WP_145124287.1\|5919509_5920430_-\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	1.20327e-37
NZ_CP036292.1\|WP_145123115.1\|5908289_5910368_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	2.09605e-143
NZ_CP036292.1\|WP_145123111.1\|5901997_5904661_+\|DUF11-domain-containing-protein	gnl\|CDD\|375050	pfam17210, SdrD_B, SdrD B-like domain. This family corresponds to the B-like domain from the SdrD protein. This domain has three calcium binding sites within a greek key beta sandwich fold.	1.5622e-14
NZ_CP036292.1\|WP_145123112.1\|5904686_5905718_-\|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.	1.04222e-106
NZ_CP036292.1\|WP_145123114.1\|5907056_5908250_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|380485	cd01543, PBP1_XylR, ligand-binding domain of DNA transcription repressor specific for xylose (XylR). Ligand-binding domain of DNA transcription repressor specific for xylose (XylR), a member of the LacI-GalR family of bacterial transcription regulators. The ligand-binding domain of XylR is structurally homologous to the periplasmic sugar-binding domain of ABC-type transporters and both domains contain the type 1 periplasmic binding protein-like fold. The LacI-GalR family repressors are composed of two functional domains: an N-terminal HTH (helix-turn-helix) domain, which is responsible for the DNA-binding specificity, and a C-terminal ligand-binding domain, which is homologous to the type 1 periplasmic binding proteins. As also observed in the periplasmic binding proteins, the C-terminal domain of the bacterial transcription repressor undergoes a conformational change upon ligand binding which in turn changes the DNA binding affinity of the repressor.	6.77827e-91
NZ_CP036292.1\|WP_145123122.1\|5920759_5922019_+\|LL-diaminopimelate-aminotransferase	gnl\|CDD\|235772	PRK06290, PRK06290, LL-diaminopimelate aminotransferase.	0
NZ_CP036292.1\|WP_145123125.1\|5924004_5924919_+\|polyphosphate-kinase-2	gnl\|CDD\|213852	TIGR03707, PPK2_P_aer, polyphosphate kinase 2, PA0141 family. Members of this protein family are designated polyphosphate kinase 2 (PPK2) after the characterized protein in Pseudomonas aeruginosa. This family comprises one of three well-separated clades in the larger family described by pfam03976. PA0141 from this family has been shown capable of operating in reverse, with GDP preferred (over ADP) as a substrate, producing GTP (or ATP) by transfer of a phosphate residue from polyphosphate. Most species with a member of this family also encode a polyphosphate kinase 1 (PPK1). [Central intermediary metabolism, Phosphorus compounds].	1.44197e-149

>NZ_CP036292.1|WP_145123120.1|5915511_5918226_+|hypothetical-protein
MCTSADNHLPQRERGGQQLVWVTLAIAVISPLFFPKYSRAQIQDSFDGGAPIWQLDRDDCGVQVIAHQRIPSGGRDAGPCESLSLQTGPGTRAEFIYRIVPTEVINELVASVWYWSQRPGARMSLRVRFPFAIDPRTGQPAVARIGNVAYTQPGQWQQLSLTNAQQQLVVQQAVLRNSMGREVDLRQPYIDAVTINTYTGPGTENVRLDDLRIDRALPVQLNRLENRSTTTMQADAATRDAFPVGVVKRFIEYNGEALPWLKANGFTGILMQRVPDAAILREANQAGLEIIAPYATVERKDLANLLAPVIAWNLGDALLEKDLPRSVDIAGRLRRLPGVLRRELVAFPIESHRQYRSVSDCLAIDLPPPVRGLTPAEESAWQSEAILSAGHAPHFLTAIASGPSGALRDQIEGLARFTDTTPIDDFGWHATWLQTMRALETSPRGIVFRSSGALDSGRAEDFQRAGVLRLINRFITLTQTIVSAGAATTELTCYDAAYRARHVRNGNLGLIIATSTSSVGTMPHAGNGKVLRIAIPPALRGQQIFRFSGMQLERMKLDATPGGSAIDVVAPDFVELFLVSNDSAATARFDRQLHQTSSQVGFDRWQLVRESLKRTTRDWDTMRQTGLSAPTDRAYAVLRQGNQALDESARVHQSGDVASAYRLLRRADAWNVQATGQLIDALAFDQDRIVSHPALHAPNSAALYIGMLPQSDNGHWQADPTVLNPFENPQLWERSGWTHDRRREDLARSDVQITERPESGRTALTLSVQSLSGQPLPGGYAGTMLRGRSQAIRCQQGDCLRIDARIRVRSQGPIRPHRGALIYDSYAGSELGLFVRPDNKWHDIRLYRVATNNQPLQTTFELIGEGELQLEQFSVSKWVPKSAPLPIRPLVGARPDALINEPVR
>NZ_CP036292.1|WP_145123119.1|5914903_5915194_-|transcriptional-regulator
MAFTAPQTSEDTPIEIQELIQAFDTLPQEHRETLAPSLLRVVECSSRRRRILNLVQEALAQLRLDMKYLVFDLEATRRERDTLRDQIEGTNNGDHE
>NZ_CP036292.1|WP_145123118.1|5913304_5914795_-|protein-kinase
MIEFTPEQLASRIIDLGLAPMAEVEAARSEVGTGESTIQDFINILHGKGLLTNLQLDKLRRGERSGYFYGKYKVMYLIGAGTFARVYRAAHRETNQVVALKVLRKRYRDEVAQMEQFLREGRMGLRLRHPNIVSIYEVDPNVKNPFMVMEFVEGETLRDLVRIRGKLQPEVAMKLLVDIASGLSYAASLGISHRDLKLSNVLVSSEGRAKLVDFGLAALADRENPEKVADCPNARAIDYAALERGTNVRKDDPRSDVFFAGAMLYTMLCGEPPLTETRERMKRLNVGRFQDIKPIGQIDPTLPVPAIQVVAKALEFDPEKRLQSAAALQLEGKQALERMKQIREGGPAVAAKVASGEMPTNEGEGRFVMLVESKASLQDVVRDRLKKRGYRVLVISDPVRALGRFVPGDDPPADCVIFSASELGSLALEAFNRFASDEHTADIPAVLLADKSQQNLIRQAKMAPHRVLLSMPLKVLELRTALRKLLAGRPKREEFI
>NZ_CP036292.1|WP_145123117.1|5912026_5913226_+|hypothetical-protein
MPSSSLCRFAILPLMWLLGIAAVGQEPLILPQPSGPSAAGTPQLLPSPSATLQQPEYPAGTVGEPIVLSDQSLTDIGYCDSGYCGSCSDDGSCVSCGTNNAHNDTFSGRLYSAFSAALCDGDPCYIPEWHLLESASFWVDSARTQNRTRVRWDYGIGMILPDRSEYFMAKIGGKGPSPQPGSASINRLDYHEMSFYTETARGKFSMFTVTPYRSLYMEQAGHGAGFGDIQIGTKSMLHDTRMLQVTLQTTTSIPTGRAKHGVGTGHVSLEPALLMGLALTDRDFLQAQAAEWIPLGGDSQYAGALLRWGVAWNRIVWQRDAKNLMTVNLDFVGWSFQDGAYTDPVLGTQSSSNGTYVYVGPGTRFLFCGKFEFGIGGLYALSEQHFAEHLMRTELTMRY
>NZ_CP036292.1|WP_145123116.1|5910829_5911750_-|hypothetical-protein
MRLALRTAATLMLAFALGLPGASVSAQQTLPASAEPEPISLSGLVVQSYPPKPTMIESMASAGRGVCAHLRASPVCQLLDGLLRPLSALTGGMIPGEKMPLPGEQEQPGPEGTAAQVKAVEMQAPQRQAAIAQLQGIDVRYYPEAEATLISALRADSSVCVRLEAAKTIATLPVCTPPLIKALQVCIAGTDVDGNPGELVPAVREQATVALNHCECCSPNLAAPANQRPEYPESRVVPAAAFASTATTIPPGAPYSMATPVAPGGTAQALFTQPVPSKPETIKPVALPVAKPKPSNLMDVFRAAAQ
>NZ_CP036292.1|WP_145123115.1|5908289_5910368_-|FAD-dependent-oxidoreductase
MQIKSIFCATAALLSLSFSHAFAKEYHHDIVIYGGTSAAVTTAVQATQMGRSVVIVSPDKHLGGLTAGGLGWTDSGNKAAIGGLSGEFYHRVWKHYQNPEAWNWEEQSKFGNRNQSGLGGDEDEARMWVFEPHVAEQIYDNWVAEEKIPVYRDQWLDRDGGVVKKEGRIKSIRTLAGDVFHGKMFVDVTYEGDLMAAASVDYHVGREANSVYGETWNGNQVGVLHHAHWFKEPIDPYIKSGDTGGKLLPGISDDPPGTRGEGDHRVQAYCFRMCLTNVPENRIPFPKPEGYDRARYQLLVRVFDSGWREMFRKFDPMPNHKTDTNNHGPFSTDNIGMNYDYPEADYERRQEIIEEHKVYQQGLMYFMANDPKVPADVREAMSKWGLPKDEFLDNGGWPHQLYIREARRMIGEYVMTEHDCLDRKETPDSIGMGSYTLDSHNVRRYVTPDGQVQNEGDIGVHLPRPYEIAYGAIVPKKSQCENLLVPVCVSSSHIAFGSIRMEPVFMILGQSAATAASIALERGEAVQDVPYQLLQQRLVDDGQVLLMDDPNRISSRKLPGVVVDDNAAKLVGSWSHSATNQKFVDSGYVHNQNEQQGERLARFETELKPGRYEVRVSYPANNNRSTMVPVKVIHAEGESTHSINQRKTPEIDGLFTKIGAFDFGSSATVEIGTQGSNGYVIADSVQFVPVTK
>NZ_CP036292.1|WP_145123114.1|5907056_5908250_+|helix-turn-helix-domain-containing-protein
MPSRHALTPPPTIPHNKQIALLIDPDDTWGRSVIQGIASAARNVLPWNLWIAPRDDQGRLRVPRNWRGDGIIAAIRDDKTAEHVDSLKLPTVIVSSWEKGPSDWHRVNTDDRKRAEMALAHFRQRGLSHFAYYGPPSQRYSPSRGQRFQEVVQQAGFSCDTYRSPSRRRDKQSLQERTLQWLHQAARPLAVFAADPHSGIVLSEVCNAVGFRVPEEIAILVGDTDDLLCEISDPPLSSIVLASEQIGMTSVGVLEKLLEGKPVAAKAQFIPPQRVIERQSSEMLAVEDPLFVDALRFIREQAHTGIQVGDVLRVVPISRRSLEQRFKQLLNCTPADEIRRIKLERVKQLLISTENTVEQIAEGSGFCGPAQLCFTFKRHVGLTPIAFRLSSRRGIAP
>NZ_CP036292.1|WP_145123113.1|5905714_5906812_-|DUF1611-domain-containing-protein
MNTTVLETSRSAVAGLDSILQYRRIAIAVGTDAPLSNCKTTISLLRYRGEHCVAVIDPAHRGKTTQEVYGVGGETPIVASIADVASPDAMFIGISPAGGAMPQSLRTTIGEGVDRGLDVISGLHEFLVEDDELWQAAQQSGSRLIDVRRNLHRKTAGGIAFRDGCLRIHAVGHDCSVGKMVTMLELERGLKERQRNAKFIATGQTGIMVVGNGVPVDCVVSDFVNGAVENLVQQNEEHDILLIEGQGSITHPAFSAVTLGLLHGCAPQGLILCYEAGRPHVKGMPHVALKSLQHYRELYEALASARSPAQVIGVAMNGRNLTAEQAEIEKREVQEQLGLPVCDVYRDGPGPLVDAVLQMQERSGS
>NZ_CP036292.1|WP_145123112.1|5904686_5905718_-|dipeptide-epimerase
MKLQWHRIELPLKDPFTIARGTMHHQQCLIVTLSHADVTGYGEVTCNRYYGHTYESLEASLQRIEGLLADCDAVHPSDLFERCQVVIPDDTFALSAVDAAAYDLYGKLHGVRTTETLGLSEPGEICSSYTLGIDSIDQMVRKYRAQPDWPIYKIKLGTPHDLDIVRALRRETEAVIRVDANCAWTPEQTITNSEALAELGVEFIEQPLPAEAPRAAQLDVFEHSRLPIIADESCRTEEDVQKCHGLFHGINIKLCKCGGLTPGSRMLRQARQLGMKTMVGCMIESTVGISAAAHLLPLLDYADLDGATLLAEDAADGVRIENGRVIFSSVPGSGIELLARSPR
>NZ_CP036292.1|WP_145123111.1|5901997_5904661_+|DUF11-domain-containing-protein
MRPLRDLLLGKSKKTTSKKKRARRGLRLESLEGRQLLAADFGGITGTVYNDLTDNGLTGDDLAPSTVTLYLFRDGGNGTFDSTAGVAGGDDVLVDTQTTDANGEYAFDRLIEGDYFVERILPAGLIAKPGSDVSAMTSITASEASGVDAGVQVDDFSEGSQSLEADAGTTSDQGFFSAPAGSQSILGRERDLMLNYTSGFRVNLDVDTNAGVLTYSSTSGAFGGYTVDYDGIDGSSSLDATGLGGVDLTNAGSADQLMVMMGADIAGVPITITVYTDAANFSTFSTVVPVTAGGVASDELLIPMTAFDTNQTGTGADFSNVGAIRAEISGAAAFDSQVSVVGTVGQTNKTVDFALYEPLTLGDLVWDDLNNNGLFDSATESGIGNVAVNLYEDTDGNGAFTPGTDLLADSTTTNASGIYTFTNLLPGDYIVQLAESNFGTGGTLNNFVSSSGVADPNNDVNDDDNGEALAGYGIVSAAITLLANSEPSTDGDADNDTNLSLDFGVVSTLDIQIVKSLSTTTPNAVAGDELTYVLTVTNAGPIDGTGVTVTDTLPASLSIVSATTSQGSVTSNGNGLTANLGDLASGATATITVVTTLAASATGTVSNTANVTSNETDSDPTNNQSTVVNTISQETDLSITKTDVGDPTSPGNTIDYTLTVTNNGPSNATGVVVTDNLPTGVTFVSGTGSQGTVTNNNGVITANVGNLASGSTATVSIRVSVASGTTGTISNQATVTGNENDPITNNNSSSTTTTVQLASLSGFSYVDADNDGVFDAGETPLEGTTVQLIGTDLLGGVVSRTTVTDATGAYAFDNLNPGTYRVVETQPAGYRDGIVTAGTGADNNGTAGSGMIDGIVLGTGDAAVNFNFGELLEMSKRRFLASFVNGQ
>NZ_CP036292.1|WP_145124287.1|5919509_5920430_-|TIM-barrel-protein
MQLGFVSAILPELSLDEVFSVAAEIGYDCVEVMCWPQGKAERRYAGITHIDTAALGPAEVDAIGALTQQHGVAISGLGYYPNPLAGDLDEAAAAVEHLHALIKACQQLSIPQLNTFVGRDWTKSVDANWPRFLETWRPIIAAAEQHGVRIGIENCPMFFTDDEWPGGKNLATTPAIWRRMFDAIPSDHFGLNFDPSHLVWQQIDHIQPVWDFADRIFHAHAKDVRVDRHRLNQVGIMANPLEYHCPKLPGLGEIDWGRFLSVLGDSGYAGPVCVEVEDRAYEGTLESRKAALRQSHDFLRNFIVKA
>NZ_CP036292.1|WP_145123122.1|5920759_5922019_+|LL-diaminopimelate-aminotransferase
MSTTNSETNSADPYFQSLFAERIGGSGYGKGTAIYKFEKIKRAKRKALADFPDRQLIDFGIGENDGVADAKVRERMAVEINQPENRGYADNGIGDFQQAVARFMQRNFNVTLDPATEINHCIGSKTALSMLPACFINPGDITLMTAPGYPVAGTHTTYYGGTVHKLPLLAENNFLPDLDSITDEIWERVKILVLNYPNSPTGRLCPPEFFEKVVKLAKEKKFIVVQDAAHIMLTFDGRPTSFLETPGAKEVGVEVHSLSKGFDMIGWRLGWVCGNPTLVRAFSDVKDNCDSGQFIAIQKAAVTALDDESIPKRVNAKYRRRLEKLVTMLNECGFECQMPGGSYFLYTKAPVASADGGSFDSGEAASQYLITQHSMVTVPWDDAGPYIRFSVTYEAADEAAEDALMAESKKRLMSAGLTF
>NZ_CP036292.1|WP_145123123.1|5922241_5922763_+|5-(carboxyamino)imidazole-ribonucleotide-mutase
MADPSPTVGVIMGSKSDWETMRHADAMLSALQIPHECKVVSAHRTPQRMFEYAQMAADRGIQVIIAGAGGAAHLPGMVASETLLPVLGVPVQSRALQGLDSLLSIVQMPGGVPVGTLSIGTSGAKNAALMAARILSLTDPALQQRLADFVAQQTADVLEDAEIENADLEDLQR
>NZ_CP036292.1|WP_145123124.1|5922759_5923902_+|5-(carboxyamino)imidazole-ribonucleotide-synthase
MNPTAIVPPGSTIGVFGSGQLGRMFTMVAKQMGYRVVIYSPDADSPAGQVADREIVAQYDDQSAVEDFARQCDVITLEFENIPVETVGWAGAITPVHPDARVLHVAQDRIIEKQTLADAGLPVTPFRPVFNADDVRRAADELGYPIVLKTARSGYDGKGQRILRDPESIEPALAELGSDRLVAEKMIDFQREVSILVYRSRNGSVGTYPLIENHHANHILDYSICPAAGSDTLRDAARQIAMTTAKSLDLVGLLCIELFVQSDDRLLINELAPRPHNSGHLTIEAFPCCQYQQLLRAICGLPLGTEPQTRPAAMANLLGDVWDGGAPAFENALAIEAVQLHLYGKQTAAPGRKMGHLTATADSIEAALANVLAARDQLKR
>NZ_CP036292.1|WP_145123125.1|5924004_5924919_+|polyphosphate-kinase-2
MSDQYAEHLNRLQEEFLDSIDEEIELELDDSRFEQLSARGEGEYDAKRLARTTYFRELLRLQRELVKLQDWVVKTNAKIVVIFEGRDAAGKGGAIKRITQRLNPRVCKVAALPAPSEREKSQWYFQRFIAHLPAGGEILLFDRSWYNRAGVERVMGFCTDKEYEDFLQTAPVFEKMLVDSGIHLIKYWFSITDEQQEFRFNCRIHDPLKQWKLSPMDLESRRRWEQYTVAKERMLQATHRPESPWWIIEADDKKRARLNCIRHLLDQIDYAEVEQSTVELPSRQREPDYERNPIPSDMIVPAFY
>NZ_CP036292.1|WP_145123126.1|5925008_5926064_-|hypothetical-protein
MRYTATEVGKVMGRTTGTIIRWARENEIGIWEEGEIQAKIVRESDIPKIAKHIGAEIPPGIVDHDNRHSVDYIVPEGYVTISQVRRTLRTASRVRQAIQELGLSKAAKIQTRRLLMGKRDVKALAKIHGLPNPFTEPHDTGSLSPSPAGFYTAKEIAKTAGIRHRRVVDLLRRYSQIVPDPTKKSRCLTTEKKFSEIAEQERMPDPFDGKAALPLDESGRPWTRYEEGSRRIFVALVHDGRAYDGEQVVLRWWCWEITPTDGYIVHAREYRSRKPCLDDALRRMGLTAKDLRVTTDPLDDIRLKAWNFRLSHDKTAKRLGISARVARRFLYGWSVRRAAESAITESMHQLI
>NZ_CP036292.1|WP_145123127.1|5926140_5926452_-|hypothetical-protein
MASTADETVDERVYTLSELAKDFGVNRTTIWRWCDREGIGRQIFPSNVTVLTKDEAEKVRGLIYDGPGNPCRERGKVGKLKATSGRRIIADAKPTGVRPRKAK
>NZ_CP036292.1|WP_145123128.1|5927048_5927504_-|DUF1569-domain-containing-protein
MSRRKIHFENLSDAAALCDQLLQSGYERNGNWSLAQICNHMRMTIDSSIDGYPKWMAIGKPLRPLLRWLMLPKLLRGDSPAGIKTASTFVPAEDLSDAEEVALFTESVRRFQSHTGYLHPHPGFGKFDHASLERFHSCHAAHHLGFLAASE
>NZ_CP036292.1|WP_145123129.1|5927652_5931015_-|helicase-SNF2
MEAIFSQRCQSEFNRGDRQRGEEYQAGGAVNILELGTLGVRAVVSGPEHDYGVLIDLEEAGDDVLFVKCTCPRFASGYLCKHIWATILELDRVQDDRLRGRGAFEIDESDMEDFEIGEPLEVSNYQPTQTALTTLQGKPAPAWLKQLNVAAQIASVKAPTVVAPPRPVETGQRSRHEFVISLADQANSSSIDLQLMRSTQDPKGRWSEPQPARISRAETVRLRDAVEQRIFTMLQWESDFPAAVAADRRVGGATRFRIHPHLVEETLAELCGSQRLAWTLDVASPKSERTPIVHGTGAAWDFAVSLAPSDSATAKPNGKRGRAKKKAMLAVMPRLERVAEKVAERREIGRVMAVCDSGVLLMDDCIAAIDPKVASWVRGWQRIGDLQLPAEEIGTFLEAFFSAPEPPRLELADALDVSIAKGKPQPKLTLSPPNDEHRTYHLVAVVSMLYGDREVQIDDHAKAVWDEASRVLMSRDVDAEIATIQILRECDFREHYPRFRDTELRISRWALPPAVIKLTGRGWLVVADGQRMRSPGEFNLEVSSGEDWFDLKAEVEFDGMAVALPTLLRSLKRRDSYVVLDDGSRGVLPEQWLNQFVDLSKAGRMEGDSVRYRRNQALLLDMLLSEQENVKTDRSFNAWRKRMRSFSGVKPADAPRGFQGELREYQKDGLGWLNFLRDFQFGGCLADDMGLGKTIQVLALLQTRRLSRPKAGQTRKPSLAVVPKSLIFNWIAEAKKFAPRLNIIDYTGNQRAALVDRLGSADLVLTTYGTLRRDVEQLTSLQFDYAILDEAQAIKNPNSQSAKAARLIDADHRLAMTGTPVENHLGDLWSLMEFLNPGMLGKLSVAQFANEEAGSQRLAGLTNALQPFILRRTKEQVLTELPEKSEQTLYCDMTPKQHKLYDELRSHYRQHLTGVVEELGLKRSKMHVLEALLRLRQTACDPRLVDGAQAAHGVKIGRLMEQLHEVTAEGHKALVFSQFTSLLALVRKELDRHGIVYEYLDGKTTRRNEHVQRFQEDPACQVFLISLKAGGHGLNLTAADYVYILDPWWNPAVESQAIDRAHRMGQTKPVLAYRLICRNTVEEKIVHLQEHKRELAEAVVTANGSLISQLSIDDLKMLFE
>NZ_CP036292.1|WP_145123130.1|5931113_5935208_+|ATP-dependent-RNA-helicase-HrpA
MPAPDTSAIDQRIAQAMRSDRFRLQRQLRQLSHVNDDPQQIERFREQLEESVALAELRAASIPQITYPEELPVSSQRDTIVELIRTRPAVIVCGETGSGKSTQLPKMCLDAGLGRSGMIGHTQPRRIAARSIASRVAEELGTSVGQLVGYKIRFADQTAPTSLIKLMTDGILLAETQSDRFLDQYDAIILDEAHERSLNIDFLLGIFSRLLQKRSDLRLIITSATIDAERFANHFRDEHGPAPIVNVEGRSYPVDIQYLPSFQSSENGDDRGQGIAAHVAAGVDEAWAHGVGDTLVFLPTERDIREVARHLGGHLRRQGLENRTDILPLYARLPASEQQKIFHGSNKPRIVLATNVAESSLTVPGIRYVVDTGTARISRYSPRSKVQRLPVEAVSRASADQRAGRCGRVGPGICIRLYDQDDYESREHFTTPEIRRTNLASVILQTKMMRLGSIDEFPFLDAPRPESISEGFRTLHEIGAIDERRELTKMGRVLGSLPVDPRVGRMIIEADQRGCLPEMLVIAAALEVQDPRIRPPEKQQAADAAHAKFVDQRSDFLSYLRIWRFYRGLQEDLSRNRLARACQTNFLGLSRMREWVDVHRQLKAMVPDLRRQQADKRGKRRRGGSERGDGEHGLSNVRVTDACEPDQATVDDNLYASIHQSLLTGLLSGVAMAGEKHQYIGIGNQEFFLWPGSGVFESKPKWIVAGELVETSKRFVRNVARIDPGWLEPLAEHLVKRSYADPFWSRKDQSAFCYERVSLFGLPIVVKRRKALAPIDPETAQRLLIDEGLVAGELVTRAKFYAHNQQLREVIAKLAHKTRRRDLIVDDYIVEHFYHAQLPSDVVDRSSLQKFDEQQPRPDWVDLCQSESDLVAWLDQPLDAGESSSLYMRPADLLPGLVEKLDPNAFPDHLQVGPTSLPLQYNFDPSADNDGVTVTIPKVLLGQISDDRLGWLVPGLIETKLIAMIKALPKRIRRNLVPAADSARRVLESLDDQMGQTAFMSTVCQRLAEIAEVPISPSDFDPDKLPESVGFYIRVVDDDGKPLGEGRDLQELRQEVIGDDEASPGSMASVVDVPDDVLQVDGLKDFTIDNLPERVERERGGVRVTLFPALVDQGDSVAVRLVDNAASAEHQMRRGLVRLFTLTDRSEINKQVRWLPGFDQAAVQLSRVIPGDSIKQGLADLIANIAFVDRQPLIRSRSEFEARRKNRGERIAMATQDIAKLLGPLAESYHGVRLSMEACKAGHLAYVRDDIKRQLSELFRDDFWLTTRMETLKQYPRYLKAISVRLEKLSSTANRDRDAHNIVAAFQDDYFRRTESYTVDRAVLDEYRWMIEELRVSLFAQTLGTAIKVSPQRLEKLRAKLDKS

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Crispr_ID: NZ_CP036292_25

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_25

5935514-5935651

Orphan

Consensus_repeat	Method
TAAAGCCTGGTGGCGCAAGCCCCAGGTTCGAAAAACGCCAACGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_25

>merge|NZ_CP036292|25|5935514-5935651|CRISPRCasFinder
TAAAGCCTGGTGGCGCAAGCCCCAGGTTCGAAAAACGCCAACGCGCAATTATGCCCCAATCCCTCCTCTCCCCAGCCACGGAGCGGCGATCGCATAAAGCCTGGCGGCGCAAGCCCCAGGTTCGAAAAACGCCAACGC

>NZ_CP036292|25|24|5935514-5935651|CRISPRCasFinder
TAAAGCCTGGTGGCGCAAGCCCCAGGTTCGAAAAACGCCAACGC	GCAATTATGCCCCAATCCCTCCTCTCCCCAGCCACGGAGCGGCGATCGCA
TAAAGCCTGGCGGCGCAAGCCCCAGGTTCGAAAAACGCCAACGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123125.1\|5924004_5924919_+\|polyphosphate-kinase-2	unknown	unknown	gnl\|CDD\|213852
NZ_CP036292.1\|WP_145123124.1\|5922759_5923902_+\|5-(carboxyamino)imidazole-ribonucleotide-synthase	unknown	unknown	gnl\|CDD\|235674
NZ_CP036292.1\|WP_145123137.1\|5942899_5946685_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123128.1\|5927048_5927504_-\|DUF1569-domain-containing-protein	unknown	unknown	gnl\|CDD\|369441
NZ_CP036292.1\|WP_145123123.1\|5922241_5922763_+\|5-(carboxyamino)imidazole-ribonucleotide-mutase	unknown	unknown	gnl\|CDD\|376377
NZ_CP036292.1\|WP_145123136.1\|5942128_5942830_+\|AIM24-family-protein	unknown	unknown	gnl\|CDD\|224924
NZ_CP036292.1\|WP_145123127.1\|5926140_5926452_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123132.1\|5936850_5938638_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224196
NZ_CP036292.1\|WP_145123129.1\|5927652_5931015_-\|helicase-SNF2	unknown	unknown	gnl\|CDD\|223627
NZ_CP036292.1\|WP_145124287.1\|5919509_5920430_-\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP036292.1\|WP_145123134.1\|5940018_5941050_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036292.1\|WP_145123135.1\|5941086_5942028_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|366542
NZ_CP036292.1\|WP_145123139.1\|5948012_5949038_-\|glutamine-synthetase	unknown	unknown	gnl\|CDD\|177922
NZ_CP036292.1\|WP_145123138.1\|5946937_5947924_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145123131.1\|5935691_5936159_-\|IS200/IS605-family-transposase	unknown	unknown	gnl\|CDD\|376616
NZ_CP036292.1\|WP_145123133.1\|5938908_5939310_-\|thioredoxin	unknown	unknown	gnl\|CDD\|379399
NZ_CP036292.1\|WP_145123140.1\|5949430_5951461_-\|S46-family-peptidase	unknown	unknown	gnl\|CDD\|371067
NZ_CP036292.1\|WP_145123130.1\|5931113_5935208_+\|ATP-dependent-RNA-helicase-HrpA	unknown	unknown	gnl\|CDD\|273900
NZ_CP036292.1\|WP_145123122.1\|5920759_5922019_+\|LL-diaminopimelate-aminotransferase	unknown	unknown	gnl\|CDD\|235772
NZ_CP036292.1\|WP_145123126.1\|5925008_5926064_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123125.1\|5924004_5924919_+\|polyphosphate-kinase-2	gnl\|CDD\|213852	TIGR03707, PPK2_P_aer, polyphosphate kinase 2, PA0141 family. Members of this protein family are designated polyphosphate kinase 2 (PPK2) after the characterized protein in Pseudomonas aeruginosa. This family comprises one of three well-separated clades in the larger family described by pfam03976. PA0141 from this family has been shown capable of operating in reverse, with GDP preferred (over ADP) as a substrate, producing GTP (or ATP) by transfer of a phosphate residue from polyphosphate. Most species with a member of this family also encode a polyphosphate kinase 1 (PPK1). [Central intermediary metabolism, Phosphorus compounds].	1.44197e-149
NZ_CP036292.1\|WP_145123124.1\|5922759_5923902_+\|5-(carboxyamino)imidazole-ribonucleotide-synthase	gnl\|CDD\|235674	PRK06019, PRK06019, phosphoribosylaminoimidazole carboxylase ATPase subunit; Reviewed.	1.4295e-177
NZ_CP036292.1\|WP_145123128.1\|5927048_5927504_-\|DUF1569-domain-containing-protein	gnl\|CDD\|369441	pfam07606, DUF1569, Protein of unknown function (DUF1569). A family of hypothetical proteins identified in Rhodopirellula baltica.	1.62336e-39
NZ_CP036292.1\|WP_145123123.1\|5922241_5922763_+\|5-(carboxyamino)imidazole-ribonucleotide-mutase	gnl\|CDD\|376377	pfam00731, AIRC, AIR carboxylase. Members of this family catalyze the decarboxylation of 1-(5-phosphoribosyl)-5-amino-4-imidazole-carboxylate (AIR). This family catalyze the sixth step of de novo purine biosynthesis. Some members of this family contain two copies of this domain.	1.06057e-83
NZ_CP036292.1\|WP_145123136.1\|5942128_5942830_+\|AIM24-family-protein	gnl\|CDD\|224924	COG2013, COG2013, Uncharacterized conserved protein [Function unknown].	3.6448e-49
NZ_CP036292.1\|WP_145123132.1\|5936850_5938638_-\|ABC-transporter-permease	gnl\|CDD\|224196	COG1277, NosY, ABC-type transport system involved in multi-copper enzyme maturation, permease component [General function prediction only].	0.00104591
NZ_CP036292.1\|WP_145123129.1\|5927652_5931015_-\|helicase-SNF2	gnl\|CDD\|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	5.70611e-114
NZ_CP036292.1\|WP_145123133.1\|5938908_5939310_-\|thioredoxin	gnl\|CDD\|379399	pfam13899, Thioredoxin_7, Thioredoxin-like. Thioredoxins are small enzymes that participate in redox reactions, via the reversible oxidation of an active centre disulfide bond.	5.76224e-09
NZ_CP036292.1\|WP_145123135.1\|5941086_5942028_+\|TIM-barrel-protein	gnl\|CDD\|366542	pfam01261, AP_endonuc_2, Xylose isomerase-like TIM barrel. This TIM alpha/beta barrel structure is found in xylose isomerase and in endonuclease IV (EC:3.1.21.2). This domain is also found in the N termini of bacterial myo-inositol catabolism proteins. These are involved in the myo-inositol catabolism pathway, and is required for growth on myo-inositol in Rhizobium leguminosarum bv. viciae.	7.38691e-26
NZ_CP036292.1\|WP_145123139.1\|5948012_5949038_-\|glutamine-synthetase	gnl\|CDD\|177922	PLN02284, PLN02284, glutamine synthetase.	9.13959e-137
NZ_CP036292.1\|WP_145123138.1\|5946937_5947924_-\|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.	1.62739e-80
NZ_CP036292.1\|WP_145123131.1\|5935691_5936159_-\|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.	2.7729e-31
NZ_CP036292.1\|WP_145124287.1\|5919509_5920430_-\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	1.20327e-37
NZ_CP036292.1\|WP_145123140.1\|5949430_5951461_-\|S46-family-peptidase	gnl\|CDD\|371067	pfam10459, Peptidase_S46, Peptidase S46. Dipeptidyl-peptidase 7 (DPP-7) is the best characterized member of this family. It is a serine peptidase that is located on the cell surface and is predicted to have two N-terminal transmembrane domains.	0
NZ_CP036292.1\|WP_145123130.1\|5931113_5935208_+\|ATP-dependent-RNA-helicase-HrpA	gnl\|CDD\|273900	TIGR01967, ATP-dependent_RNA_helicase_HrpA, RNA helicase HrpA. This model represents HrpA, one of two related but uncharacterized DEAH-box ATP-dependent helicases in many Proteobacteria and a few high-GC Gram-positive bacteria. HrpA is about 1300 amino acids long, while its paralog HrpB, also uncharacterized, is about 800 amino acids long. Related characterized eukarotic proteins are RNA helicases associated with pre-mRNA processing. The HrpA/B homolog from Borrelia is 500 amino acids shorter but appears to be derived from HrpA rather than HrpB. [Unknown function, Enzymes of unknown specificity].	0
NZ_CP036292.1\|WP_145123122.1\|5920759_5922019_+\|LL-diaminopimelate-aminotransferase	gnl\|CDD\|235772	PRK06290, PRK06290, LL-diaminopimelate aminotransferase.	0
NZ_CP036292.1\|WP_145123134.1\|5940018_5941050_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	2.90158e-20

>NZ_CP036292.1|WP_145123130.1|5931113_5935208_+|ATP-dependent-RNA-helicase-HrpA
MPAPDTSAIDQRIAQAMRSDRFRLQRQLRQLSHVNDDPQQIERFREQLEESVALAELRAASIPQITYPEELPVSSQRDTIVELIRTRPAVIVCGETGSGKSTQLPKMCLDAGLGRSGMIGHTQPRRIAARSIASRVAEELGTSVGQLVGYKIRFADQTAPTSLIKLMTDGILLAETQSDRFLDQYDAIILDEAHERSLNIDFLLGIFSRLLQKRSDLRLIITSATIDAERFANHFRDEHGPAPIVNVEGRSYPVDIQYLPSFQSSENGDDRGQGIAAHVAAGVDEAWAHGVGDTLVFLPTERDIREVARHLGGHLRRQGLENRTDILPLYARLPASEQQKIFHGSNKPRIVLATNVAESSLTVPGIRYVVDTGTARISRYSPRSKVQRLPVEAVSRASADQRAGRCGRVGPGICIRLYDQDDYESREHFTTPEIRRTNLASVILQTKMMRLGSIDEFPFLDAPRPESISEGFRTLHEIGAIDERRELTKMGRVLGSLPVDPRVGRMIIEADQRGCLPEMLVIAAALEVQDPRIRPPEKQQAADAAHAKFVDQRSDFLSYLRIWRFYRGLQEDLSRNRLARACQTNFLGLSRMREWVDVHRQLKAMVPDLRRQQADKRGKRRRGGSERGDGEHGLSNVRVTDACEPDQATVDDNLYASIHQSLLTGLLSGVAMAGEKHQYIGIGNQEFFLWPGSGVFESKPKWIVAGELVETSKRFVRNVARIDPGWLEPLAEHLVKRSYADPFWSRKDQSAFCYERVSLFGLPIVVKRRKALAPIDPETAQRLLIDEGLVAGELVTRAKFYAHNQQLREVIAKLAHKTRRRDLIVDDYIVEHFYHAQLPSDVVDRSSLQKFDEQQPRPDWVDLCQSESDLVAWLDQPLDAGESSSLYMRPADLLPGLVEKLDPNAFPDHLQVGPTSLPLQYNFDPSADNDGVTVTIPKVLLGQISDDRLGWLVPGLIETKLIAMIKALPKRIRRNLVPAADSARRVLESLDDQMGQTAFMSTVCQRLAEIAEVPISPSDFDPDKLPESVGFYIRVVDDDGKPLGEGRDLQELRQEVIGDDEASPGSMASVVDVPDDVLQVDGLKDFTIDNLPERVERERGGVRVTLFPALVDQGDSVAVRLVDNAASAEHQMRRGLVRLFTLTDRSEINKQVRWLPGFDQAAVQLSRVIPGDSIKQGLADLIANIAFVDRQPLIRSRSEFEARRKNRGERIAMATQDIAKLLGPLAESYHGVRLSMEACKAGHLAYVRDDIKRQLSELFRDDFWLTTRMETLKQYPRYLKAISVRLEKLSSTANRDRDAHNIVAAFQDDYFRRTESYTVDRAVLDEYRWMIEELRVSLFAQTLGTAIKVSPQRLEKLRAKLDKS
>NZ_CP036292.1|WP_145123129.1|5927652_5931015_-|helicase-SNF2
MEAIFSQRCQSEFNRGDRQRGEEYQAGGAVNILELGTLGVRAVVSGPEHDYGVLIDLEEAGDDVLFVKCTCPRFASGYLCKHIWATILELDRVQDDRLRGRGAFEIDESDMEDFEIGEPLEVSNYQPTQTALTTLQGKPAPAWLKQLNVAAQIASVKAPTVVAPPRPVETGQRSRHEFVISLADQANSSSIDLQLMRSTQDPKGRWSEPQPARISRAETVRLRDAVEQRIFTMLQWESDFPAAVAADRRVGGATRFRIHPHLVEETLAELCGSQRLAWTLDVASPKSERTPIVHGTGAAWDFAVSLAPSDSATAKPNGKRGRAKKKAMLAVMPRLERVAEKVAERREIGRVMAVCDSGVLLMDDCIAAIDPKVASWVRGWQRIGDLQLPAEEIGTFLEAFFSAPEPPRLELADALDVSIAKGKPQPKLTLSPPNDEHRTYHLVAVVSMLYGDREVQIDDHAKAVWDEASRVLMSRDVDAEIATIQILRECDFREHYPRFRDTELRISRWALPPAVIKLTGRGWLVVADGQRMRSPGEFNLEVSSGEDWFDLKAEVEFDGMAVALPTLLRSLKRRDSYVVLDDGSRGVLPEQWLNQFVDLSKAGRMEGDSVRYRRNQALLLDMLLSEQENVKTDRSFNAWRKRMRSFSGVKPADAPRGFQGELREYQKDGLGWLNFLRDFQFGGCLADDMGLGKTIQVLALLQTRRLSRPKAGQTRKPSLAVVPKSLIFNWIAEAKKFAPRLNIIDYTGNQRAALVDRLGSADLVLTTYGTLRRDVEQLTSLQFDYAILDEAQAIKNPNSQSAKAARLIDADHRLAMTGTPVENHLGDLWSLMEFLNPGMLGKLSVAQFANEEAGSQRLAGLTNALQPFILRRTKEQVLTELPEKSEQTLYCDMTPKQHKLYDELRSHYRQHLTGVVEELGLKRSKMHVLEALLRLRQTACDPRLVDGAQAAHGVKIGRLMEQLHEVTAEGHKALVFSQFTSLLALVRKELDRHGIVYEYLDGKTTRRNEHVQRFQEDPACQVFLISLKAGGHGLNLTAADYVYILDPWWNPAVESQAIDRAHRMGQTKPVLAYRLICRNTVEEKIVHLQEHKRELAEAVVTANGSLISQLSIDDLKMLFE
>NZ_CP036292.1|WP_145123128.1|5927048_5927504_-|DUF1569-domain-containing-protein
MSRRKIHFENLSDAAALCDQLLQSGYERNGNWSLAQICNHMRMTIDSSIDGYPKWMAIGKPLRPLLRWLMLPKLLRGDSPAGIKTASTFVPAEDLSDAEEVALFTESVRRFQSHTGYLHPHPGFGKFDHASLERFHSCHAAHHLGFLAASE
>NZ_CP036292.1|WP_145123127.1|5926140_5926452_-|hypothetical-protein
MASTADETVDERVYTLSELAKDFGVNRTTIWRWCDREGIGRQIFPSNVTVLTKDEAEKVRGLIYDGPGNPCRERGKVGKLKATSGRRIIADAKPTGVRPRKAK
>NZ_CP036292.1|WP_145123126.1|5925008_5926064_-|hypothetical-protein
MRYTATEVGKVMGRTTGTIIRWARENEIGIWEEGEIQAKIVRESDIPKIAKHIGAEIPPGIVDHDNRHSVDYIVPEGYVTISQVRRTLRTASRVRQAIQELGLSKAAKIQTRRLLMGKRDVKALAKIHGLPNPFTEPHDTGSLSPSPAGFYTAKEIAKTAGIRHRRVVDLLRRYSQIVPDPTKKSRCLTTEKKFSEIAEQERMPDPFDGKAALPLDESGRPWTRYEEGSRRIFVALVHDGRAYDGEQVVLRWWCWEITPTDGYIVHAREYRSRKPCLDDALRRMGLTAKDLRVTTDPLDDIRLKAWNFRLSHDKTAKRLGISARVARRFLYGWSVRRAAESAITESMHQLI
>NZ_CP036292.1|WP_145123125.1|5924004_5924919_+|polyphosphate-kinase-2
MSDQYAEHLNRLQEEFLDSIDEEIELELDDSRFEQLSARGEGEYDAKRLARTTYFRELLRLQRELVKLQDWVVKTNAKIVVIFEGRDAAGKGGAIKRITQRLNPRVCKVAALPAPSEREKSQWYFQRFIAHLPAGGEILLFDRSWYNRAGVERVMGFCTDKEYEDFLQTAPVFEKMLVDSGIHLIKYWFSITDEQQEFRFNCRIHDPLKQWKLSPMDLESRRRWEQYTVAKERMLQATHRPESPWWIIEADDKKRARLNCIRHLLDQIDYAEVEQSTVELPSRQREPDYERNPIPSDMIVPAFY
>NZ_CP036292.1|WP_145123124.1|5922759_5923902_+|5-(carboxyamino)imidazole-ribonucleotide-synthase
MNPTAIVPPGSTIGVFGSGQLGRMFTMVAKQMGYRVVIYSPDADSPAGQVADREIVAQYDDQSAVEDFARQCDVITLEFENIPVETVGWAGAITPVHPDARVLHVAQDRIIEKQTLADAGLPVTPFRPVFNADDVRRAADELGYPIVLKTARSGYDGKGQRILRDPESIEPALAELGSDRLVAEKMIDFQREVSILVYRSRNGSVGTYPLIENHHANHILDYSICPAAGSDTLRDAARQIAMTTAKSLDLVGLLCIELFVQSDDRLLINELAPRPHNSGHLTIEAFPCCQYQQLLRAICGLPLGTEPQTRPAAMANLLGDVWDGGAPAFENALAIEAVQLHLYGKQTAAPGRKMGHLTATADSIEAALANVLAARDQLKR
>NZ_CP036292.1|WP_145123123.1|5922241_5922763_+|5-(carboxyamino)imidazole-ribonucleotide-mutase
MADPSPTVGVIMGSKSDWETMRHADAMLSALQIPHECKVVSAHRTPQRMFEYAQMAADRGIQVIIAGAGGAAHLPGMVASETLLPVLGVPVQSRALQGLDSLLSIVQMPGGVPVGTLSIGTSGAKNAALMAARILSLTDPALQQRLADFVAQQTADVLEDAEIENADLEDLQR
>NZ_CP036292.1|WP_145123122.1|5920759_5922019_+|LL-diaminopimelate-aminotransferase
MSTTNSETNSADPYFQSLFAERIGGSGYGKGTAIYKFEKIKRAKRKALADFPDRQLIDFGIGENDGVADAKVRERMAVEINQPENRGYADNGIGDFQQAVARFMQRNFNVTLDPATEINHCIGSKTALSMLPACFINPGDITLMTAPGYPVAGTHTTYYGGTVHKLPLLAENNFLPDLDSITDEIWERVKILVLNYPNSPTGRLCPPEFFEKVVKLAKEKKFIVVQDAAHIMLTFDGRPTSFLETPGAKEVGVEVHSLSKGFDMIGWRLGWVCGNPTLVRAFSDVKDNCDSGQFIAIQKAAVTALDDESIPKRVNAKYRRRLEKLVTMLNECGFECQMPGGSYFLYTKAPVASADGGSFDSGEAASQYLITQHSMVTVPWDDAGPYIRFSVTYEAADEAAEDALMAESKKRLMSAGLTF
>NZ_CP036292.1|WP_145124287.1|5919509_5920430_-|TIM-barrel-protein
MQLGFVSAILPELSLDEVFSVAAEIGYDCVEVMCWPQGKAERRYAGITHIDTAALGPAEVDAIGALTQQHGVAISGLGYYPNPLAGDLDEAAAAVEHLHALIKACQQLSIPQLNTFVGRDWTKSVDANWPRFLETWRPIIAAAEQHGVRIGIENCPMFFTDDEWPGGKNLATTPAIWRRMFDAIPSDHFGLNFDPSHLVWQQIDHIQPVWDFADRIFHAHAKDVRVDRHRLNQVGIMANPLEYHCPKLPGLGEIDWGRFLSVLGDSGYAGPVCVEVEDRAYEGTLESRKAALRQSHDFLRNFIVKA
>NZ_CP036292.1|WP_145123131.1|5935691_5936159_-|IS200/IS605-family-transposase
MSSTHTNLLFHIVYSTKYRRDMIGADVQPRLYEYIGGVVREHKGILLEVGGMPDHVHLLAKLSPAVAISDVLRFVKANSSKWVNETLAPKLPFAWQRGFGAFSVSASNVLEVTSYIQTQAEHHRKLTFRDEYRALLERHGIEFDERYLFEEEHVA
>NZ_CP036292.1|WP_145123132.1|5936850_5938638_-|ABC-transporter-permease
MASVFALIPLQQVSWLSSWLTPIWILAIGMLLGLVATAAIYLVLAALSRIPALGNLAEDTRKATFVAMGIAIVVAGLGILKTVVFADSPEITVAGEENPTAAHSAYLILPMVGLGVIVGWGLVFGFWKRTIREFFQIAREGITGYLLMALVGFIILGLAPTMLVTDRDKILSSLPAVLESDRWETTITLDPAPADLPADQSPFQRHDLVQYDPEAVSEVVIVSDRTIMIADAESPDNFTMSPQRFESDDPVVWRRGKENPLIRSVLPLPLDPTNGVYFQNREVDPATVKIAIVTKPAAPEALTIWVTAFIVVLLLTAMITIRQAAPQVSAIALATAKSELAQPLYVTLLLIGFAAIVLFIWVPFHTLGEDIKVLKDSGMTLIMIFSIIQAVWSSGTSVSEEIEGRTALTVLSKPVSRQSFMIGKYLGIMWTILLMFVILGLLLMVVTAYKPIYDSRENTTEQPPWQTCHLEMVTTAPGLCLLFMETTLIAGISVAIATRLPVIANFVICFTIYVIGNITSPIVRASAEDNELVRFVGRLIAVVFPNLNTFNVQAAVDAGNPIPPIYLAGAFTYLACFMVVVLVVSLLLFEDRDLA
>NZ_CP036292.1|WP_145123133.1|5938908_5939310_-|thioredoxin
MFSVLLTALLSVVASEQAPSPDYATAYRSAQEEGKPLMVVVGADWCPACVNLKQNTIASLKQAGDLEGVEMAIVNRDTQPGLAGKLMRGPMMPQIIVFSKGNAGSWTRTQLTGFQTRDSLRSLIKRAVRNKGT
>NZ_CP036292.1|WP_145123134.1|5940018_5941050_+|Gfo/Idh/MocA-family-oxidoreductase
MRLRVGVIGLGPAWQHRHRPALMMMRDRFQVRAIYAPVAHLAAQAARDFEAETMDGYRALIHRSDIDAVIVLDSSWQGWLPLVAACEAGKAVYWASDLNIDAHRAAQLKEQVDKSGIAFMAEFPRRYAPATLRLKELLATTLGKPQLLFCHRRLGRTEPTSTNLVSDVPQHQERTTRELVEIVDWCRYVVADNPTHLNSTVYGEPGKEAYRQLSMRFGTGPGAVCAQISAGQYVPSSWQEAIGFRPSADMQICCEHGLAFIDLPSTLVWFDDAGRHVESLETELPVGEQLLIQFHRSVTSLVRKMANLQDAHYALQVIRLAQQSAETGQRICLNELFSPTPPI
>NZ_CP036292.1|WP_145123135.1|5941086_5942028_+|TIM-barrel-protein
MHDSHFTAQSPLSRRQLLTSSIAAASLAAISPQLAGAAEMIPGRHAPKFKFSLAAYSYRSLLQGKGDAAPKMDLLGFIDECARMQLDGVELTSYYMPEEPTEAYLIGLRSHCFRQGLAVSGTAIRNDFGHSETATRNRELEHVRRWIDHAATLHAPMIRIFAGHGQKGNSPEQTHELMVEGIQKSCEYAGKHGIYLALENHGGVTASADGLLKLVRDVDSPWLGVNLDTGNFRFGGEPYEQMEAVAKYAVNVQVKVVVKDADGKPQPMDFPRLKKILTDANYRGFVVLEYEEPGDVPAECRRYVQQMRTDLAL
>NZ_CP036292.1|WP_145123136.1|5942128_5942830_+|AIM24-family-protein
MSDGRYTLDAFLEKTRDRDLNQGLFELESDRMLDINLDGEVWIKLGAMVAYTGQVKFEREGILSRGIGNMLKKAVSGEGTSLTKATGNGSVFCADAGKKITILQLQNNAICVNGNDLLAFEMSLKYDIKMMKRMTSMLAGGLFNIRLEGTGMVAITSHYDPMTLPVTPAQPVTTDPNATVLWSGNLEPELKTDVQLKTFFGRGSGESVQLQFRGNGFVVVQPYEEVYFQHGGS
>NZ_CP036292.1|WP_145123137.1|5942899_5946685_-|hypothetical-protein
MLLDALPSTLYSQEIELRVRVHWQTALPERPALAVEIDSGRLGRLRNLSLDAGSTGGLDLSPDRKQISIHSRTASLRGGVEFVAHGTPEAILTLRQSPVGGDAADPPTGSTVILADLIDQPQELELAGGRIKLVIARAPGDRLHVQLDRENLLFRPSESVPLKIVPNATGLAPNQKLRLLMTLTKARSNKPILQREWQVATDADGKVAPVDAGPLTIPDAEAAYDINVRLTSERRYLALEVPWAQDSGSIERSVQFVVVSDAPPVEDLRPFIEVARIEPTKRQWWNPVWMPDRLIPGKLVPDAIPSIVPARQQPLSSEPLTHIAWQDHVVSELQPGGWQSYPLQIKDPGKPHVLVVRYPNDRAMRLGVSVLEPNASGKVIPLGVDSGVAVLPKAIASQPELLEHRVVFWPKTRQPMVLLTNFDSSKPAWFASLSIEAGPDTLAAQDDLADGGIDPDEPHRLTALYLDKPLLADTFGCTRSLDPDGATLIDDWQTFLEAGQRLVQYVKWAGFNGAIITVNSEGTSLYPTDTMSATARHDMGIFSSRGIDPNKKDVLELLLRMFDRSGLKLVPAVELATPLTALERQLRDSKESLGIEPINSAGHRYVDISSAEHGLAPFYNPLDRRVQNAITDVIAELQTRYGSHASLHGVGLHLGGKTYMQLPGIDWGVDQRTLDEFRSTLSGAPVSNNQMIGWIERDGQGAFLDWRGRRLAGMFSQLAKAAGNRPVLLLTADWMSDTAAGANDPQRRALDAGIDWESIGGAAGVIPMRLHRSQPLADHARQSVDALLAQDTLWDNHLAALPASGAMLMRPPTDVRLGAFESQSPWGAENTQAWLFAHGVFSSDDGKRTLAQILMPADANVLAVGGWTTPRGSEAASRQFLQCYRALPPGRFESVQSEDPEAAQLAIVRRLRTQDGFYLYALNPAPWMVQVKIELNNPEEAAIHPLGRRGSELPKSRTLVETLRPGQLVAYRIDSPKADIVVWNVEIPGLPALREHLGVQLQRLTQTVGTLGQPKPYEGLANRDFEQSAATQSDIPGWLSAQHPAGSVQLVVAAGVLGSQAVQLTNSGETNAKTWLLSHPFKAPASGRLAVHARVRRDTKTDMVRLRMSLEGRYRDRSIRRSTVIGEAPEGVPNSDWSSMPFRLEVTDLPVEGLEELRIAFDLASPGKVWIDDVMLYDQFLTSDERKELQSRVFVAVERMRGGDLSACGRLLDSYWGRHVLGLPAEQLEVTDTVDQTDPPLETAPSIADRLRQWLPSPIWR
>NZ_CP036292.1|WP_145123138.1|5946937_5947924_-|protein-kinase
MADHTSTGIVLSATDHRLPDPMPVGLSKYTNFKDMAEGGSGKLRSCWDTVVNRLVVMKTLQPKFIHDPKENRRFLREARITAMLQHPNTVPVYEIGHDPEVGIYFTMKRISGENFFQALKRIAMGDEATTEAYSLQRRIEIAISAAQALAYAHVRGVIHRDVKPENIWIGNFGEVILLDWGVAKVWGHSDESESFLFRREDVEDEEMQLRTLTGGGQRPGTPLYMSPEQVRGYKYLDERSDIFSMGIVLYEMLAIREPFRGRNINETFNNIQNVDPPKPSERSPDREIPPAADEIVMKAIQKKPTARYQSMRAMIDDMHELLENRKFS
>NZ_CP036292.1|WP_145123139.1|5948012_5949038_-|glutamine-synthetase
MTKCKLEYVWLDGYQPTQLLRSKTKIEDDFSGNVEDAKMWSFDGSSTEQATGGKSDLLLKPVKVIPDPGRIGTGFLVMCEVLNSDGTPHKTNGRATIADDDGDFWFGFEQEYTLWDSETQKPVGFPEQGFPAPQGPYYCSVGGGRAVGREIVEEHLELCLQAGLNVEGINAEVMLGQWEFQIFAKGARDAGDQIWLARYLLDRTAESHGVEINYHCKPVKGDWNGSGMHANFSNSLLRTCGSQEVYEAVCQAFEPRIKEHIDVYGADNDQRLTGLHETQSIDKFSYGVSDRGASIRIPIFTVEHGWKGWLEDRRPASNADPYMVASAIIATVKSAKLPVNA
>NZ_CP036292.1|WP_145123140.1|5949430_5951461_-|S46-family-peptidase
MNKVSLVLAFLLSSSSFADEGMWLFNDLPNEYLRDRYSFKADDAWVKRLMQASVRLNSGGSGSFVSSDGLVLTNHHVASDTLHKLSTADRNLIEEGFLARSHEQELKAPDLEINQLVEIIDVTEKVAAAVTPAMSPEHAVTARRAVIAEIEKDSLDRTGLRSDVVTLFGGAQYHLYRYKKYTDVRLVWAPETSIAFFGGDADNFEYPRYCMDATILRVYEQGKPAKIENFLPWSDTEIDEHELVFVSGHPGRTQRIFTVEALKYLRDHRLPYVLDYLRRKEVLMQQFGLRGKEESRRAQDELFGIQNSRKAYGGMLAGLQDPKTMQEKVRRQQRVLEAVRSKQPEAAAAWETIARLQQQRVEILDQTSGFRSRLYDLAETLVLMAAEDKKPNSERLPELRVSNRDSLLQDLLSTAPIYNDLEQVKLTDELMRLAERRGGDDPLVVEILDGKRPDVRAAELVFGTKVGDLETRKQFVEVGAPLIDKSEDPMILLARAMQGEYQRLRKIRDELDEQEKQAYTQITEASLAAGSTSKYPDATFTLRLAIGTIKGYSQNGVEVPAWTKMEGIFDYAAKHAGQEDYELPESWQRAAAAIPRATPMNFVCTADIIGGNSGSPVVNRAGELVGLIFDGNIQSLTADYIYTSDQARAVSVSAAAIRVALEKIYGAPFLADQLGR

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Crispr_ID: NZ_CP036292_26

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_26

6477600-6477695

Orphan

Consensus_repeat	Method
CGCCCTCCGGGCTATCCAAACCGCTCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_26

>merge|NZ_CP036292|26|6477600-6477695|CRISPRCasFinder
CGCCCTCCGGGCTATCCAAACCGCTCGATTCTCAGGCCGGAGGCCGACACAATGTGAGTAAGAGTGTGTCGCCCTCCGGGCTATCCAATCCGCTCG

>NZ_CP036292|26|25|6477600-6477695|CRISPRCasFinder
CGCCCTCCGGGCTATCCAAACCGCTCG	ATTCTCAGGCCGGAGGCCGACACAATGTGAGTAAGAGTGTGT
CGCCCTCCGGGCTATCCAATCCGCTCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123445.1\|6466494_6468171_+\|DUF1553-domain-containing-protein	unknown	unknown	gnl\|CDD\|377876
NZ_CP036292.1\|WP_145102126.1\|6483707_6484028_+\|P-II-family-nitrogen-regulator	unknown	unknown	gnl\|CDD\|223424
NZ_CP036292.1\|WP_145123447.1\|6469628_6470912_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237171
NZ_CP036292.1\|WP_145123459.1\|6487681_6489160_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|238872
NZ_CP036292.1\|WP_145123446.1\|6468199_6469501_+\|DUF1501-domain-containing-protein	unknown	unknown	gnl\|CDD\|369346
NZ_CP036292.1\|WP_145123452.1\|6476980_6477454_-\|putative-toxin-antitoxin-system-toxin-component,-PIN-family	unknown	unknown	gnl\|CDD\|379205
NZ_CP036292.1\|WP_145124307.1\|6474369_6475698_-\|matrixin-family-metalloprotease	unknown	unknown	gnl\|CDD\|334067
NZ_CP036292.1\|WP_145123453.1\|6477900_6480093_-\|peroxidase	unknown	unknown	gnl\|CDD\|376988
NZ_CP036292.1\|WP_145102122.1\|6481082_6482069_-\|AAA-domain-containing-protein	unknown	unknown	gnl\|CDD\|223786
NZ_CP036292.1\|WP_145123460.1\|6489492_6490005_-\|YaiI/YqxD-family-protein	unknown	unknown	gnl\|CDD\|367134
NZ_CP036292.1\|WP_145123455.1\|6482203_6483541_-\|histidine--tRNA-ligase	unknown	unknown	gnl\|CDD\|273080
NZ_CP036292.1\|WP_145123454.1\|6480557_6480860_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377419
NZ_CP036292.1\|WP_145123450.1\|6475807_6476242_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369610
NZ_CP036292.1\|WP_145123457.1\|6484677_6485955_-\|tyrosine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235645
NZ_CP036292.1\|WP_145123451.1\|6476690_6477035_-\|toxin-antitoxin-system-HicB-family-antitoxin	unknown	unknown	gnl\|CDD\|310261
NZ_CP036292.1\|WP_145123458.1\|6486056_6487658_-\|aldehyde-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|143447
NZ_CP036292.1\|WP_145123449.1\|6473552_6474227_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274375
NZ_CP036292.1\|WP_145123456.1\|6484189_6484636_-\|DUF4430-domain-containing-protein	unknown	unknown	gnl\|CDD\|379618
NZ_CP036292.1\|WP_145123444.1\|6465817_6466144_+\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|239606
NZ_CP036292.1\|WP_145123448.1\|6470908_6473566_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123445.1\|6466494_6468171_+\|DUF1553-domain-containing-protein	gnl\|CDD\|377876	pfam07587, PSD1, Protein of unknown function (DUF1553). A family of proteins found in Rhodopirellula baltica.	6.60003e-29
NZ_CP036292.1\|WP_145102126.1\|6483707_6484028_+\|P-II-family-nitrogen-regulator	gnl\|CDD\|223424	COG0347, GlnK, Nitrogen regulatory protein PII [Amino acid transport and metabolism].	1.35574e-28
NZ_CP036292.1\|WP_145123447.1\|6469628_6470912_-\|hypothetical-protein	gnl\|CDD\|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	0.000175922
NZ_CP036292.1\|WP_145123459.1\|6487681_6489160_+\|hypothetical-protein	gnl\|CDD\|238872	cd01834, SGNH_hydrolase_like_2, SGNH_hydrolase subfamily. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	0.000443558
NZ_CP036292.1\|WP_145123446.1\|6468199_6469501_+\|DUF1501-domain-containing-protein	gnl\|CDD\|369346	pfam07394, DUF1501, Protein of unknown function (DUF1501). This family contains a number of hypothetical bacterial proteins of unknown function approximately 400 residues long.	1.25231e-97
NZ_CP036292.1\|WP_145123452.1\|6476980_6477454_-\|putative-toxin-antitoxin-system-toxin-component,-PIN-family	gnl\|CDD\|379205	pfam13470, PIN_3, PIN domain. Members of this family of bacterial domains are predicted to be RNases (from similarities to 5'-exonucleases).	1.63899e-21
NZ_CP036292.1\|WP_145124307.1\|6474369_6475698_-\|matrixin-family-metalloprotease	gnl\|CDD\|334067	pfam00413, Peptidase_M10, Matrixin. The members of this family are enzymes that cleave peptides. These proteases require zinc for catalysis.	1.03282e-40
NZ_CP036292.1\|WP_145123453.1\|6477900_6480093_-\|peroxidase	gnl\|CDD\|376988	pfam03098, An_peroxidase, Animal haem peroxidase.	0
NZ_CP036292.1\|WP_145102122.1\|6481082_6482069_-\|AAA-domain-containing-protein	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	1.30074e-98
NZ_CP036292.1\|WP_145123460.1\|6489492_6490005_-\|YaiI/YqxD-family-protein	gnl\|CDD\|367134	pfam02639, DUF188, Uncharacterized BCR, YaiI/YqxD family COG1671.	2.03241e-51
NZ_CP036292.1\|WP_145123455.1\|6482203_6483541_-\|histidine--tRNA-ligase	gnl\|CDD\|273080	TIGR00442, hisS, histidyl-tRNA synthetase. This model finds a histidyl-tRNA synthetase in every completed genome. Apparent second copies from Bacillus subtilis, Synechocystis sp., and Aquifex aeolicus are slightly shorter, more closely related to each other than to other hisS proteins, and actually serve as regulatory subunits for an enzyme of histidine biosynthesis. They were excluded from the seed alignment and score much lower than do single copy histidyl-tRNA synthetases of other genomes not included in the seed alignment. These putative second copies of HisS score below the trusted cutoff. The regulatory protein kinase GCN2 of Saccharomyces cerevisiae (YDR283c), and related proteins from other species designated eIF-2 alpha kinase, have a domain closely related to histidyl-tRNA synthetase that may serve to detect and respond to uncharged tRNA(his), an indicator of amino acid starvation; these regulatory proteins are not orthologous and so score below the noise cutoff. [Protein synthesis, tRNA aminoacylation].	9.21491e-149
NZ_CP036292.1\|WP_145123454.1\|6480557_6480860_+\|hypothetical-protein	gnl\|CDD\|377419	pfam04894, Nre_N, Archaeal Nre, N-terminal. This conserved region is found in the N-terminal region of archaeal Nre proteins. While most archaeal organisms encode only a single Nre protein, some encode two, NreA and NreB.	0.00979206
NZ_CP036292.1\|WP_145123450.1\|6475807_6476242_-\|hypothetical-protein	gnl\|CDD\|369610	pfam07946, DUF1682, Protein of unknown function (DUF1682). The members of this family are all hypothetical eukaryotic proteins of unknown function. One member is described as being an adipocyte-specific protein, but no evidence of this was found.	0.000298279
NZ_CP036292.1\|WP_145123457.1\|6484677_6485955_-\|tyrosine--tRNA-ligase	gnl\|CDD\|235645	PRK05912, PRK05912, tyrosyl-tRNA synthetase; Validated.	0
NZ_CP036292.1\|WP_145123451.1\|6476690_6477035_-\|toxin-antitoxin-system-HicB-family-antitoxin	gnl\|CDD\|310261	pfam05534, HicB, HicB family. This family consists of several bacterial HicB related proteins. The function of HicB is unknown although it is thought to be involved in pilus formation. It has been speculated that HicB performs a function antagonistic to that of pili and yet is necessary for invasion of certain niches.	0.000994368
NZ_CP036292.1\|WP_145123458.1\|6486056_6487658_-\|aldehyde-dehydrogenase-family-protein	gnl\|CDD\|143447	cd07129, ALDH_KGSADH, Alpha-Ketoglutaric Semialdehyde Dehydrogenase. Alpha-Ketoglutaric Semialdehyde (KGSA) Dehydrogenase (KGSADH, EC 1.2.1.26) catalyzes the NAD(P)+-dependent conversion of KGSA to alpha-ketoglutarate. This CD contains such sequences as those seen in Azospirillum brasilense, KGSADH-II (D-glucarate/D-galactarate-inducible) and KGSADH-III (hydroxy-L-proline-inducible). Both show similar high substrate specificity for KGSA and different coenzyme specificity; KGSADH-II is NAD+-dependent and KGSADH-III is NADP+-dependent. Also included in this CD is the NADP(+)-dependent aldehyde dehydrogenase from Vibrio harveyi which catalyzes the oxidation of long-chain aliphatic aldehydes to acids.	0
NZ_CP036292.1\|WP_145123449.1\|6473552_6474227_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274375	TIGR02984, Sig-70_plancto1, RNA polymerase sigma-70 factor, Planctomycetaceae-specific subfamily 1. This group of sigma factors are members of the sigma-70 family (TIGR02937) and are apparently found only in the Planctomycetaceae family including the genuses Gemmata and Pirellula (in which seven sequences are found).	5.27649e-74
NZ_CP036292.1\|WP_145123456.1\|6484189_6484636_-\|DUF4430-domain-containing-protein	gnl\|CDD\|379618	pfam14478, DUF4430, Domain of unknown function (DUF4430). Although this family has overlaps with SLBB, the majority of its sequences are unique. Several family members, eg UniProtKB:A0RGA8, that do not overlap have an LPXTG-cell wall anchor at their C-terminus, a SSF_Family 10_polysaccharide_lyase or Glycosyltransferase structure associated with them in the middle region, as shown by InterPro, as well as this domain at the N-terminus.	1.49654e-13
NZ_CP036292.1\|WP_145123444.1\|6465817_6466144_+\|Rieske-2Fe-2S-domain-containing-protein	gnl\|CDD\|239606	cd03530, Rieske_NirD_small_Bacillus, Small subunit of nitrite reductase (NirD) family, Rieske domain; composed of proteins similar to the Bacillus subtilis small subunit of assimilatory nitrite reductase containing a Rieske domain. The Rieske domain is a [2Fe-2S] cluster binding domain involved in electron transfer. Assimilatory nitrate and nitrite reductases convert nitrate through nitrite to ammonium.	4.49474e-26
NZ_CP036292.1\|WP_145123448.1\|6470908_6473566_-\|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.	1.48889e-84

>NZ_CP036292.1|WP_145123452.1|6476980_6477454_-|putative-toxin-antitoxin-system-toxin-component,-PIN-family
MWRRYVSHPLKIVCPPVVLDTNVLVAGACRHEQSMAYRVLMAVLNRRVPLMLTEGIIAEYTDVLSRPTVRKLTGLTAKQNSDLVLELISLSHQTQLRFSWRPNLSDEADNKFIEAAVAATAIIITYNVRDFDCAALVKHGWDVMTPVEFSTLYDLGN
>NZ_CP036292.1|WP_145123451.1|6476690_6477035_-|toxin-antitoxin-system-HicB-family-antitoxin
MGCDDTSRIFDTLRFRKLTMATLSLRMRDDLKAKAQQLASEQGVSLNSYINATLAATVAQAETLAMMGDKFDGVDRDRLRARVMKFMSATQSGPEPTPVEIERAIAGKSDVGSR
>NZ_CP036292.1|WP_145123450.1|6475807_6476242_-|hypothetical-protein
MTFKRALMLAGLVTATILLAGNDAQAQCSGGRGGASGGSAGTGYALGQRYDPLAYQRDYALQQQRYLQNQQLYAMRQQTYQQQVAQKYQQRQDLLAARKERAMLKREARDARIAQLKAARQAEREAEASASESYASAETVVAMR
>NZ_CP036292.1|WP_145124307.1|6474369_6475698_-|matrixin-family-metalloprotease
MSQKRKPLQRRKSRILVTETLESRRVLTASVGWDGPGLGNAELTYNISGSPSSLTQAETDAAIETALNAWSSVVDVSFTPTDQSGLRDSIDISFTNIDGDGGTLAQAYFPDDVNPARIAGDIQFDSSEVWEVGNSLGNQAFDLVWVAVHEIGHALGLDHLDDASAVLAPFVSPSQSFAGLSSEDIAEITSLYAAADDSILPVDDSDATTDLVDTSDDDTTDDDTLDSGDTENEETLDPVDDGTETVDDPTAEDDDSLEPVDDGGVLDGGETDETDETDAHCLDGSRFRFGVGLGLTGATAEDLLTRLDTNKDGELTEEDVSSRLWDRLVDAEIDADGDAVITLAEVEAALATAREDFFSALDANEDGLLTADEVSDRFWEKVSDADSDADEAVSLDELSTWLDDGNSLHRRGGHHSHRGFHHCVDAAFSLLGRAASQRGFFR
>NZ_CP036292.1|WP_145123449.1|6473552_6474227_-|sigma-70-family-RNA-polymerase-sigma-factor
MIATDSTHRSDSSSQSGQTQEFRSLLEAARDGDSEALGRLLQWYSNYLTLLASTQLDRRLQRRLNPSDIVQEAMLAAHRDFGDFRGQSQGELLCWLRQILIHTLHRAFAANVKVAKRDVRREVSLDAVANGLENSAINLASILPNRGESPSAPMQARERAVWLADQLSELHPPYRDVIVFRVLQGMSFDEIAKRMDRSGGAVRMLWLRALEAFKTQGEARDVCE
>NZ_CP036292.1|WP_145123448.1|6470908_6473566_-|protein-kinase
MSVNDSVLDSCDEPELLRALDDDQKQRLTEQLDRYLQSLESGEPLDLETLDRENPDLSEVFASYLSKLDALYGVAVGFQDPTDQFSDLQPTSGSPMTLGDFTVQREIGRGGMGVVYEANQKSLNRQVALKLLPMASLLDARQIARFKNEARAAGLLQHPHIVPVYSVGSERGIHYFAMQLIDGLPVDAWILQQRESASTSRDWRSIVAWAIDIADALHYAHTSGVVHRDVKPSNLLLDSAGKIWIADFGLARCQDDRSLTVSGDLLGTMRYMSPEQATGKAEAVDHRTDIYSLAATLFEMLTLRTAVVGEDGPTLLRAIQQDEPPRLRSLLPHTPADLSVVLQKAMARRKDDRYESADQLAADLRAVLDGRPTLAKPPTVVARVGRWTARHRRSVAVAASVCAVAMLWLVASSLIILQKSNDAKWSAVQRDQYFRHAQSAVDHLGTEVAEQLASVPGAEQVRHSLLLQTLRYHEQFAAQATGDPELSAEVARTHSRIGTIVKELKSPRDAIGHFRRAAEGYAAIIERPESIPAELAAVETRYHAAQNLNHLGLALADIGESDEALQNYRQTLAIQGALVQSDPENERYAAEFALTTNNLALLFIQNGDVAQARPLLDDAIARLTTIVERKPEDELAARGLASALANRSAVTVDDPRSEIELLQRAIQIRAASVGESSNRLSASGELATLLNNLGSANMHAGRWASAEQAFTRAAGLQRQLLSIAPAIDQHRRDLATSLNNVARALQKQAKHAEAIEALDEAISLQQASLELSNGDASGHSRIGAMLHNRGSSMLALGELAAAERQWKQAIDQQQLALAIDPQHAEAKRFLPTHYSSLLRCLARGKRWQAIDAVAVSYRAAAAGNGAAEKQADRDLAAVNELAVAQ
>NZ_CP036292.1|WP_145123447.1|6469628_6470912_-|hypothetical-protein
MKAPLKRSSSRRLRLEQLEGRWMLSANPLTLASDDLGYRGDQGDRFSDTQIVDSGSRGGGPRDAAAQQGNDRGGPESRDSGDREDSRSGRLDDQRPGGERRGGDRNGDRPPPRRDRGSSDGTPTITDNDQSSTTLPDVVNVTIRTETSSTSIGDSTSPIRTPVVSSSGPGVDSNPAVPGLSGEQGDLGPMQADVDGVSETVLVSVTPQGELWELSPESFDQVLRAESETFANPSTVEAIEAVDQWLNQSDAFRDQIEQLDQAIEDLAEEDPAAEPEAFELPEGTELQPDTAAEAVPPESNSQQWLLETSGLLLENDSSSRTVADPQPPRSGESIANADAGWNVGIGVFKAFESVLPAAPQRSLSSALLPTVATPPRIPSPVEPTAESDSQRSLAWYEAASLAVITIAGVVYMRRSRTETVRNSADFV
>NZ_CP036292.1|WP_145123446.1|6468199_6469501_+|DUF1501-domain-containing-protein
MNIDCGSHDHLSRRSLLQSAGALSMTALANQLARGSEQSSKPVRPKSVIILWLKGAPSQYETFDPHAGTKYGGEVAAIDTTARDVQISEFLPQTAEQMHRVALVRSVTSKEGDHERAFYNIQTGWRPDPTVVHPSIGSIVCHELPGGADIPRHISILPDNSAGRGGYLGAKYDAFKVYDPANKVPDIRPYVGEKRFQRRVDGLMDVVESNFRKGRLRDLDRDRTLHGIATKSALTMMDSDQLAAFEVDKESKALRAQFGETAFGRGCLAAARLIEVGVRCVEVGLSGWDTHADNHNGQRTQCEILDPAYATLLQVLADRDLLDSTLVVCGGEFGRTPKINPVGGRDHWPHGFSIALAGCGLRQGIVHGATSPDPKLDNKENDLLTNVGDPVTVQDIHATILKALDVQFERELITPIGRPLKLSEGTPIESILS
>NZ_CP036292.1|WP_145123445.1|6466494_6468171_+|DUF1553-domain-containing-protein
MKWYQSLARWTLLAAVGLLGIGYLANGLSGDGRSTQPPPIPKASTASETADWMEVVADVDAEFETTWTRESLSRAPDADWQTVSRRISLALIGSSISLEDMRWLESLPEGTQVDALTERLLADHRFADYWAERLGRAYVGADIGPFIVYRRRRFITWLSQQLHDRVPYSQIVRKLITAKGIWTENPQVNFLTVTLDTTEKGRVDPVRLAARTSRAFLGMRIDCLQCHDDFLGNVTLGTNSDPLEGTQRDFHHLAAFYSTAANSIQGIRDDGKTYEYQFLYEDETEEVEPIVPFLPELLTTDPAAEKLPSRQQLARWVTHPENIPAARAAVNRVWALMFGKPLSDPVDDIPLHGPFPAGLDRLAHDFAEHDWDLRRLIRIISHLQTFQLDSRCDFEVTSEHEQAWAVYPLIRLRPEQVASSIIQSCRLATLDRQSALLVQLHALGEKHDFINRYGDTGEDEFGQDAITITQRLLAMNGKLVNERTGKNPFMNASSQIAMFATDDAHAVEITYLSILNRRPTEEEAAAWVRQSEQGVSRRQFVEDLFWILINSSEFSWNH
>NZ_CP036292.1|WP_145123444.1|6465817_6466144_+|Rieske-2Fe-2S-domain-containing-protein
MNAAENWTTIAKSEEIEEGIGREFLVGTRIVAVFRVDGELFAIDGICPHQGGPLADGAVRDGCVTCPWHGWQFELTSGRHTISGRSLAETFPIRDRDGIVELIVADEV
>NZ_CP036292.1|WP_145123453.1|6477900_6480093_-|peroxidase
MKPADTFRALYNSLWSKSNRASKRPRRRRRRLRSETLESRQMLAADLNLFQHNYFDAEDVNDDGIVSPVDALAILNAIQRNQRDEGGMFTDVNNDGRRGPIDALRVLNRINRGGQDRHDSPIDNGSTIPDLPDEVRSIDGTGNNLEDEDLGAAGTTLLRVADADYADGISEPGGEDRPSAREISNVLSDASVDSEGNDRGLSAFLYVWGQFIDHDIDLSLSQEDGETFDIVVPAGDPYFDPSGTGEVTIGLSRSVYDLTTGTSVDNPREQVNAITAYIDGSQVYGSDQETADGLRSFEGGRLVITDDGLLPLDESGMVIAGDIRASENISLTAIQTLFAREHNRLADEISAADPDLIDEEIYQQARAIVIAEIQSITYNEFLPALLGNNAVDSYDGYDASVNPSIANEFSTAAFRFGHSTLNDDIEFFDNDGLEVRDEISLTEAFFNPSLLEETGIDSILKYDASSQSMQIDLEVVDSLRNFLFGPPGAGGFDLVSLNIQRGRDHGLADYNSTRVAYGLDPVESFADITSDVELQGKLESLYGDVNNIDLWVGLLAEDHVRGASVGETHQAIISDQFERIRDGDRFWYENVFEGRELKELQQTTLADIIERNTNVEGLQENVFFMNATVSGTVTRAVDNSASNRSRSSSLNRNNNSSRDVAVEGVELELLDDEGNVIDSTTTDRKGSYRFSNFVHTGEYQIRLAETGETLDLLVSNGATRLRGLDFEIVV
>NZ_CP036292.1|WP_145123454.1|6480557_6480860_+|hypothetical-protein
MTDPILIRFGMATWFSFMLTNLSIAAMGIELRRRGVPIRWLSYSLNMRVRLEKINEVTAAYWEFKRERGEFPLFACALLTAALGLLVIPFTALLYRLLAN
>NZ_CP036292.1|WP_145102122.1|6481082_6482069_-|AAA-domain-containing-protein
MTAPQIDEQIAQYSQTCTKLIDEVGRVLVGQEAMVSRLLIGMLTGGHILLEGVPGLAKTLTVSSLAKAIHTGFSRIQFTPDMLPADVIGTEVFNPKEATYSIKQGPIFSNLILADEINRAPAKVQAALLEAMQERQVTIGTETFRFEDPFLVMATQNPIDQEGTYPLPEAQVDRFMLKVMVDYPTRDEERKVVDRMAGGKPMPEISAIATPEDIMGARGVVEKIWCDDKVRDYVVDVVRATRNPAELGVRGLEGMIETGASPRGSLNLMKASKAHAFLQGRNYITPHDVKSLAPDVLRHRVMLSYEAEAEGKTVDDCIRQILDNVPVP
>NZ_CP036292.1|WP_145123455.1|6482203_6483541_-|histidine--tRNA-ligase
MSLITPRTLRGFRDYLPEVMMPRERCMEIAREVFRSFGFAPIDTPALEYLEVLTGKGSDETDRQLYQFTDQGNRQVGMRFDLTVPFARFAAQHINELGTPFKRYHIAPVWRGEKSQAGRYREFIQCDFDTIGTQSVAADIETPLVIHSLMLALGFEAFKIHINDRRVLTGLLGHLGIAEHSVLVLRALDKLAKIGADKVAQEMQDTAGVSESQARAVLALAEIDVDADDLYAQLSKITGENATAALGIERLQQMREGLAAAGVPASRVKLDLTIARGLDYYTGVIFETFLDALPSIGSVCSGGRYDNLAELFTKQHLPGVGASLGLDRLLAAMEQLEMLPQVRTPAPVFIPYFDKGQLNAYLQLAATVRAAGIGVEVFPEPKKLGQQLKYADGRGFTLALIAGNQEFEAGTCQVKDLRDKSTTDVQWSADQPEPLLDAIRSKLKS
>NZ_CP036292.1|WP_145102126.1|6483707_6484028_+|P-II-family-nitrogen-regulator
MKQVIAVVKPYLAQKVLGSLERAPIEAITVTEVKGFGRQKSYLDQYGDSEYSEAFLPKVEITAWVEDARVEEILAKLVSVARSGRMGDGKIFVMPVLGFLEEPSGT
>NZ_CP036292.1|WP_145123456.1|6484189_6484636_-|DUF4430-domain-containing-protein
MMFVCQTVSVASLQRIAGIGCLLLLALVGCQNATEPAAAPPADGPKIAVRFVFEFGEGEPVEVALDAVPDGSTVADAMRQIAEMPDTVQLEIVGKGDMTFVQSINGKTTSGNEGWSYYVNEEWAQEGVGAIELEDGDLVRWTYGESEF
>NZ_CP036292.1|WP_145123457.1|6484677_6485955_-|tyrosine--tRNA-ligase
MTDILSELRWRNLIHQVTDEAGLAKLLSEGSQSVYAGFDPTADSLHVGSLLPLMMLRRFQRAGHRPVALVGGATGMIGDPSGKSEERNLLSADQLEKNVAGIASQVQSFLDSDGDNAAQLVNNFDWMKNFSYLNFLRDVGKNFPVGVMMGKESVKSRLTSEAGLSYTEFSYMLLQAYDFVELNKKLGCRVQLGGSDQWGNITAGIDLGRRMGTPQLYGMTSPLLLTSDGRKMGKTERGTIWLSAERTSPYEFFQYWRNVDDKDVMTCLHYLTEIDREECESLAQELENNAGAAVAQKRLAEWLTQLVHGDAGLKSALNASQILFGGEISDLSDKELTQIFADVPSKELPKSALEGEGLWVVEAFKTSGLVSSNGEARRAVQEGSAYINNQRQQDIDYKLTRADLASESVMVLRRGKKKYALLRFV
>NZ_CP036292.1|WP_145123458.1|6486056_6487658_-|aldehyde-dehydrogenase-family-protein
MSTTAQSEPVLIAGQWRPASLDTANTNVFQATDPSNMELLSPVFPVSSWQDCDEALNAAAAAYAELRQLPRERIAAFLEAFADRIDAAKDRLVAAANRETGLPASPRLADVELPRTTNQLRLAAAACRSGDWAAATIDTKAGIRSCYQSLGPVCVFGPNNFPFAFGSLSGGDFAAAIAAGNPVIGKANSSHPETTKIFAEEAFAALQATDLPTATVQLIYRLNHADGERLVADPRVGATGYTGSRGAGLALKAAADRAGKPIYLELSSVNPVAILPGAMVERGDAIIKDFVGSALMGTGQFCTSPGIILMTKGENADKFVEAVSAAYQAATPGTLLSPAVTKSLGAGIQTLRDAGAELVCGGGDPVEGRCARSNTLLKTTGEKFLSDPETFQTEAFGNASMVVVADDIDQLTQVIDSLEGNLTGCIYSANDGSDDAVYPQVAFALEPKVGRILNDKMPTGVAVSPAMNHGGPYPSTGHPGFTAVGIPAALPRFAKLTCFDAVRPARLPELLQDKNPTGSTWRFIDGQWSQADV
>NZ_CP036292.1|WP_145123459.1|6487681_6489160_+|hypothetical-protein
MYPINKASKHIARAGFWRVCRARGIAFRLIALAIGLLPLLMIESTLWVLDLPRAESRIEAIGEANGTRRLFVLNRATGRYEIAPDRLNLFRPDSFVAEKPADLRRVFVLGGSTVQGRPYQIETAFSTWLGLALQTCDPQHRWEVVNCGGVSYASYRVAAILDEVLQYQPDAIILYIGHNEFLERQSFGQLQRLPDWIVPALSAVERMRTFQLLRSQIFADAALEPSTRELLTHNVEALLDNQGGLAEYHPDAPPRGAVEEAFADNLDAMIAYCRQRNVPVIVCCPARNLVDCPPFKSEPLVPLDDSDQRAFDVAMATATDEQAAAADRIAALRTAQALDPQNPSVAYRLGRLMLQAGEIETARQQLTLAADNDSCPLRIRSSMQSQIRAIAAQRQVPLLDVDRLMQSHSRNGLVGAKWMVDHVHPTVHGHQMIADALLEILVDQWLTTSDVDCQSNREAAYADHLRSLDESYFVRGQQRLEGLKQWAAGRAR
>NZ_CP036292.1|WP_145123460.1|6489492_6490005_-|YaiI/YqxD-family-protein
MKIWIDADAAPMDVKQIVFRAAKRLDVETILVANRMMEVPASLSMVRSIQVREGADQADRYIAAEGQRGDLAITADLPLAGDLVEKGLFVIDPRGEEYSPETITSRLSMRNFMDDLRGAGMVVGRTAPYGETDKKAFAATFDRLLTRALRLAERAKKKSASSGEATEEES

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Crispr_ID: NZ_CP036292_27

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_27

6731666-6731770

Orphan

Consensus_repeat	Method
GGCGATCGCATAAAGCCTGCGGCGCAAGCCGCAGGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_27

>merge|NZ_CP036292|27|6731666-6731770|CRISPRCasFinder
GGCGATCGCATAAAGCCTGCGGCGCAAGCCGCAGGAAAGCGTCCCGCAAAAATCAAAAGCCACGGATGTGGCGATCGCGTAAAGCCTGCGGCGCAAGCCGCAGGA

>NZ_CP036292|27|26|6731666-6731770|CRISPRCasFinder
GGCGATCGCATAAAGCCTGCGGCGCAAGCCGCAGGA	AAGCGTCCCGCAAAAATCAAAAGCCACGGATGT
GGCGATCGCGTAAAGCCTGCGGCGCAAGCCGCAGGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123618.1\|6724371_6725385_+\|dihydrofolate-reductase	unknown	unknown	gnl\|CDD\|238127
NZ_CP036292.1\|WP_145123624.1\|6736331_6739631_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273344
NZ_CP036292.1\|WP_145123613.1\|6717111_6717696_+\|3-isopropylmalate-dehydratase-small-subunit	unknown	unknown	gnl\|CDD\|179314
NZ_CP036292.1\|WP_145123617.1\|6719982_6723840_+\|aldehyde-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|143443
NZ_CP036292.1\|WP_145123629.1\|6744156_6744720_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123631.1\|6745615_6747856_+\|polyribonucleotide-nucleotidyltransferase	unknown	unknown	gnl\|CDD\|236995
NZ_CP036292.1\|WP_145123627.1\|6742480_6743083_+\|peptide-methionine-(R)-S-oxide-reductase-MsrB	unknown	unknown	gnl\|CDD\|234692
NZ_CP036292.1\|WP_145123630.1\|6745028_6745298_+\|30S-ribosomal-protein-S15	unknown	unknown	gnl\|CDD\|180170
NZ_CP036292.1\|WP_145123620.1\|6726069_6727512_+\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|379862
NZ_CP036292.1\|WP_145123616.1\|6719416_6720082_-\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|239518
NZ_CP036292.1\|WP_145124318.1\|6731143_6731617_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|131643
NZ_CP036292.1\|WP_145123622.1\|6732368_6734174_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275381
NZ_CP036292.1\|WP_145123614.1\|6717705_6718008_+\|DUF167-domain-containing-protein	unknown	unknown	gnl\|CDD\|376843
NZ_CP036292.1\|WP_145123621.1\|6727523_6731012_+\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	unknown	unknown	gnl\|CDD\|226220
NZ_CP036292.1\|WP_145123623.1\|6734270_6735827_-\|altronate-dehydratase	unknown	unknown	gnl\|CDD\|377287
NZ_CP036292.1\|WP_145123615.1\|6718112_6719297_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|181731
NZ_CP036292.1\|WP_145123626.1\|6741371_6742379_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|226359
NZ_CP036292.1\|WP_145123619.1\|6725464_6725911_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|236558
NZ_CP036292.1\|WP_145123625.1\|6739707_6740949_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123628.1\|6743277_6744003_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123618.1\|6724371_6725385_+\|dihydrofolate-reductase	gnl\|CDD\|238127	cd00209, DHFR, Dihydrofolate reductase (DHFR). Reduces 7,8-dihydrofolate to 5,6,7,8-tetrahydrofolate with NADPH as a cofactor. This is an essential step in the biosynthesis of deoxythymidine phosphate since 5,6,7,8-tetrahydrofolate is required to regenerate 5,10-methylenetetrahydrofolate which is then utilized by thymidylate synthase. Inhibition of DHFR interrupts thymidilate synthesis and DNA replication, inhibitors of DHFR (such as Methotrexate) are used in cancer chemotherapy. 5,6,7,8-tetrahydrofolate also is involved in glycine, serine, and threonine metabolism and aminoacyl-tRNA biosynthesis.	2.02193e-48
NZ_CP036292.1\|WP_145123624.1\|6736331_6739631_+\|hypothetical-protein	gnl\|CDD\|273344	TIGR00927, retinal_rod, K+-dependent Na+/Ca+ exchanger. [Transport and binding proteins, Cations and iron carrying compounds].	4.85301e-11
NZ_CP036292.1\|WP_145123613.1\|6717111_6717696_+\|3-isopropylmalate-dehydratase-small-subunit	gnl\|CDD\|179314	PRK01641, leuD, 3-isopropylmalate dehydratase small subunit.	6.73769e-128
NZ_CP036292.1\|WP_145123617.1\|6719982_6723840_+\|aldehyde-dehydrogenase-family-protein	gnl\|CDD\|143443	cd07125, ALDH_PutA-P5CDH, Delta(1)-pyrroline-5-carboxylate dehydrogenase, PutA. The proline catabolic enzymes of the aldehyde dehydrogenase (ALDH) protein superfamily, proline dehydrogenase and Delta(1)-pyrroline-5-carboxylate dehydrogenase (P5CDH, (EC=1.5.1.12 )), catalyze the two-step oxidation of proline to glutamate; P5CDH catalyzes the oxidation of glutamate semialdehyde, utilizing NAD+ as the electron acceptor. In some bacteria, the two enzymes are fused into the bifunctional flavoenzyme, proline utilization A (PutA) These enzymes play important roles in cellular redox control, superoxide generation, and apoptosis. In certain prokaryotes such as Escherichia coli, PutA is also a transcriptional repressor of the proline utilization genes.	0
NZ_CP036292.1\|WP_145123631.1\|6745615_6747856_+\|polyribonucleotide-nucleotidyltransferase	gnl\|CDD\|236995	PRK11824, PRK11824, polynucleotide phosphorylase/polyadenylase; Provisional.	0
NZ_CP036292.1\|WP_145123627.1\|6742480_6743083_+\|peptide-methionine-(R)-S-oxide-reductase-MsrB	gnl\|CDD\|234692	PRK00222, PRK00222, peptide-methionine (R)-S-oxide reductase MsrB.	4.6983e-79
NZ_CP036292.1\|WP_145123630.1\|6745028_6745298_+\|30S-ribosomal-protein-S15	gnl\|CDD\|180170	PRK05626, rpsO, 30S ribosomal protein S15; Reviewed.	2.11438e-46
NZ_CP036292.1\|WP_145123620.1\|6726069_6727512_+\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|379862	pfam16576, HlyD_D23, Barrel-sandwich domain of CusB or HlyD membrane-fusion. HlyD_D23 is the combined domains 2 and 3 of the membrane-fusion proteins CusB and HlyD, which forms a barrel-sandwich. CusB and HlyD proteins are membrane fusion proteins of the CusCFBA copper efflux system in E.coli and related bacteria. The whole molecule hinges between D2 and D3. Efflux systems of this resistance-nodulation-division group - RND - have been developed to excrete poisonous metal ions, and in E.coli the only one that deals with silver and copper is the CusA transporter. The transporter CusA works in conjunction with a periplasmic component that is a membrane fusion protein, eg CusB, and an outer-membrane channel component CusC in a CusABC complex driven by import of protons.	9.25873e-09
NZ_CP036292.1\|WP_145123616.1\|6719416_6720082_-\|NUDIX-domain-containing-protein	gnl\|CDD\|239518	cd03426, CoAse, Coenzyme A pyrophosphatase (CoAse), a member of the Nudix hydrolase superfamily, functions to catalyze the elimination of oxidized inactive CoA, which can inhibit CoA-utilizing enzymes. The need of CoAses mainly arises under conditions of oxidative stress. CoAse has a conserved Nudix fold and requires a single divalent cation for catalysis. In addition to a signature Nudix motif G[X5]E[X7]REUXEEXGU, where U is Ile, Leu, or Val, CoAse contains an additional motif upstream called the NuCoA motif (LLTXT(SA)X3RX3GX3FPGG) which is postulated to be involved in CoA recognition. CoA plays a central role in lipid metabolism. It is involved in the initial steps of fatty acid sythesis in the cytosol, in the oxidation of fatty acids and the citric acid cycle in the mitochondria, and in the oxidation of long-chain fatty acids in peroxisomes. CoA has the important role of activating fatty acids for further modification into key biological signalling molecules.	1.5753e-45
NZ_CP036292.1\|WP_145124318.1\|6731143_6731617_+\|hypothetical-protein	gnl\|CDD\|131643	TIGR02594, hypothetical_protein, TIGR02594 family protein. Members of this protein family known so far are restricted to the bacteria, and for the most to the proteobacteria. The function is unknown.	0.00849221
NZ_CP036292.1\|WP_145123622.1\|6732368_6734174_-\|hypothetical-protein	gnl\|CDD\|275381	sd00034, LRR_AMN1, leucine-rich repeats, antagonist of mitotic exit network protein 1-like subfamily. A leucine-rich repeat (LRR) is a structural protein motif of 20-30 amino acids that is unusually rich in the hydrophobic amino acid leucine. The conserved eleven-residue sequence motif (LxxLxLxxN/CxL) within the LRRs corresponds to the beta-strand and adjacent loop regions, whereas the remaining parts of the repeats are variable. LRRs fold together to form a solenoid protein domain, termed leucine-rich repeat domain. Leucine-rich repeats are usually involved in protein-protein interactions.	3.00576e-15
NZ_CP036292.1\|WP_145123614.1\|6717705_6718008_+\|DUF167-domain-containing-protein	gnl\|CDD\|376843	pfam02594, DUF167, Uncharacterized ACR, YggU family COG1872.	3.51249e-28
NZ_CP036292.1\|WP_145123621.1\|6727523_6731012_+\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	gnl\|CDD\|226220	COG3696, COG3696, Putative silver efflux pump [Inorganic ion transport and metabolism].	0
NZ_CP036292.1\|WP_145123623.1\|6734270_6735827_-\|altronate-dehydratase	gnl\|CDD\|377287	pfam04295, GD_AH_C, D-galactarate dehydratase / Altronate hydrolase, C-terminus. Family members include the C termini of D-galactarate dehydratase (EC:4.2.1.42) which is thought to catalyze the reaction D-galactarate = 5-keto-4-deoxy-D-glucarate + H2O, and altronate hydrolase (altronic acid hydratase, EC:4.2.1.7), which catalyzes D-altronate = 2-keto-2-deoxygluconate + H2O. As purified, both enzymes are catalytically inactive in the absence of added Fe2+, Mn2+, and beta-mercaptoethanol. Synergistic activation of altronate hydrolase activity is seen in the presence of both iron and manganese ions, suggesting that the enzyme may have two ion binding sites. Mn2+ appears to be part of the enzyme active centre, but the function of the single bound Fe2+ ion is unknown. The hydratase has no Fe-S core.	0
NZ_CP036292.1\|WP_145123615.1\|6718112_6719297_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|181731	PRK09257, PRK09257, aromatic amino acid transaminase.	0
NZ_CP036292.1\|WP_145123626.1\|6741371_6742379_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|226359	COG3839, MalK, ABC-type sugar transport systems, ATPase components [Carbohydrate transport and metabolism].	4.06656e-135
NZ_CP036292.1\|WP_145123619.1\|6725464_6725911_+\|hypothetical-protein	gnl\|CDD\|236558	PRK09545, znuA, zinc ABC transporter substrate-binding protein ZnuA.	0.00796675

>NZ_CP036292.1|WP_145124318.1|6731143_6731617_+|hypothetical-protein
MTGCNPADTPTDDATPTAESAADDHGHDHSGTDHSEVGHGHGVGPHDGTIADWGGGKFHVEFTVDHDKTEATVYVLGGDEKTAAPIAAESIELTIIDPEMQVTLKPSPQEGDPDGTASRFIGTHEKLGVVQEYAGTMTGVIDGTPYTGEFKEEAHTH
>NZ_CP036292.1|WP_145123621.1|6727523_6731012_+|CusA/CzcA-family-heavy-metal-efflux-RND-transporter
MLDAVIHFSLRYRMLVVVISLALLVYGSYQAAQMPIDVFPDLDRPRVVIITEAPGLATEEVETLVTQPIEIALIGANGVQAVRSQTTAGLNVIYIEFDWSTQIRAARQTVQERLTTLQGILPAGIRPQMTPPSSIMGQIVIAGIYRQPGPRGGKLAVVGKTSMMAERIDSADPAEAIQVWQPVERKDLKTWKRVETQSITWTAAAADDPQLAGESPEGVGIATIQIAGQEHDVNFYSDAKRQLDLRTVADWIIRPRLLKTTGVAEVFMQGGDRKQYQILIDPTALLEYDVTVQDVAQALRESNINTSGGFAVTGETERSIRILGRLGPESRVVIEDLKKIPVGYHPKRSVLLEQVARVSEGPQLKRGDGSVDGQPGIVFTTVKQPHVDTRQLTNDIAAAFAEVEASLPADIIINSELFRLKNFIDRGIFNVAEALVIGAFLVMVVLFLFLLNFRTTFITLTAIPLSLVITTLVFRWIGWFSGSELSINVMTLGGIAVAMGELVDDAIVDVENIFRRLKENNAAPTRRAAIQVVFEASKEIRSAIMFGTAVVILVFLPLFALSGVEGRLFAPLGLAYIISILASFLVSLTVTPALSYYLLPKSSATHRDHDGLLLRGLKRATTPWIQLSMAWPRMLLCATWLGVLLAAWQMAQLGRNFLPPFDEGSVQVNVTLPPGSSLETSNRVSQTIDAVFQSMQKNEDRPEGEILHFVRRTGRAELDEHASPVNVGEYILSMNPEVDQDREEILAGLLKKLKDEAPGVDIEVEQPLAHLISHMVSGIYAQIAIKIHGDDLDTLQRIAEQVKSTLQSIPGITPPVVEPIQQVPELHIQLRSDDLALHGLTRQYVADVLQIALQGEVVSQVLEGQRRFDLMVRLEEAYRTDYANLGRLRIDLPDHPGYADRGQIELQEIANIGEGSGPNSVNREDARRRIAVRCNTQGRDLASAVGEIKQRIDRQIQLPIGYYIEYGGQFESQQRATQWIIALAGVSVVGMFVVLMLLFPSVRIVLQILNALPTAFIGGVLALVITDQSLTVASLVGFISLGGIAVRNGILLVTHYFHLMKEEGESFTQAMVLRGSLERLAPVLMTALTAGIGLIPLVLGGQEPGREILYPVATVILGGLTTSTFCEFLIHPGLFWAFSGKDAAALASGTAEDVDSQFEPPT
>NZ_CP036292.1|WP_145123620.1|6726069_6727512_+|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MQHVPSLTKLLFGLALAAGVALTTWYFRDVLPFAGSVPAVAKEDPPQPASEKQTILEISVQARKNLGLTSQPARPQTYWRSLQIPGKLADRPGVSDRGVTSPAESVVTEIHISPGDAIRPGERLFTLRLFSEYLQATQTQLFKAKQETSIIQADIDRVSDAVTSGAVVRSKMIELQGNLRRQQILIEAARQDLRSRGLDSAQIEQIESGRFLSTIDVRAPEALPTVPLTETNTDRAARTIQPVQQARFDSSSSRAPEFAFEVQELLVELGQQVQAGQPLATLANHQALYVVGHAFKREAPFLEQAAQEGRAIDIEFADDATDQWPELEQRFEIRHLSNAIDTNSRTFDFFIPLRNQSRAYQKAEQTFLVWRFRPGQRVRLHVPVEKLENVLVLPAAAVVRDGPEAYVFMQNGDLFKRLPVHVLHEDRQSIVLANDGSVTPGTYLAQNAAASLNRVLRSQAASGQQVGVHVHPDGTVHAAH
>NZ_CP036292.1|WP_145123619.1|6725464_6725911_+|hypothetical-protein
MRPLLSLLLIATFMLGHVVPHSHAASGGAEPGDHAHRPHVHLSHGHDHDHGHHHGQADRPSAGEESPADALTELSLACDHDGDAVYFVDSDWTVARNAVSISLDLSSLPFTSIAGTIPQRERQYRRSSGPPDRRPKLPIYLLTASLRL
>NZ_CP036292.1|WP_145123618.1|6724371_6725385_+|dihydrofolate-reductase
MRVQDDRCRNAQERTVRDAANVCKTLCQGRVRRSDGGLLRRRRLPNRRGRFAARGEGEHDRFRETVPNAGAEVSWNRYPIDRCCVGRWQGQRNHDGGVYDQGGYDRRIEVLARTSSSFNLEEWQDHRPEVLLRPQFLNTLCPPMRLPIAFVAGEPLSPRLPRTCSQGKVWFCRFPKQGAPSGMIIISAMSEDRVIGSQNGMPWNVPAEYQQYLDFVAGQTVIMGRKTFEIFGKDVAPETSLIVVSRSAELDDVPVATTFDKAVAMAKALGKQIFIAGGSSIYEQAIAVADQMYLSTIHGQYSGDAYFPAFDADNWQVVETREQPQFTFRRWKRKTTS
>NZ_CP036292.1|WP_145123617.1|6719982_6723840_+|aldehyde-dehydrogenase-family-protein
MLGCKRSAFATVVPLSGSSVARAAAVRRVGLLASNNSKRRIDTVSSSASDPAAEESPFLNLNEAVAATESAASGLTGWQRDAARAIALAKQLLQRSQQLLTPAERRQQSELDRMIGHHEDKATLIEMTDQAFRTDVPQRVADQLTHILDVQGVPRFFSPLDRTLLRGFQTFGGYLPGVAVPMVKDKMRHETANVILPAEKEVLEKHLRERQREGIRMNVCLLGEALLGEGETRQRLKKYLAALQMPEIECISVKVSTIYSQISTLARSHTESVIADRLELLYRAAMRQTFQRRDGTQTSKFVYLDMEEYRDLHLTVDVLKRTLDRPELSQVRAGIALQSYIPDSFDVLQDLAQWAQRRTAAGGLPLTIRVVKGANMEMERVEASIEGWPQAPYTTKHETDANYKRMIRTILAPENSTALRLGVASHNLFDIALVAIWASEADALQRVQFEMLEGMANQQRRALFEMTGSMLLYAPACEQTDFLNAIGYLIRRLDENTGQENFLRHAFQLQPGTETWRTLADGFRASLVAIDSVTTKPRRQQDRSQVPERPEVGETWQQFINEPNTDWSLPQNSRWAQELLASWRDRCDDAATRIPLSIAGREVTDAREIAESRDPSRPGKIACRYAMATSDDIDAAIACARQDPRNWRSMPSEARRATLHDAAQLLRQRRGDLLAAALIDGGKTLAESDPEVSEAIDFIEFYSLCADQAYQSPQIQASGVGVVAVISPWNFPIAIPCGGVAAALAAGNTVLLKPASETVLPAYLLCQAFWDAGVPREALQLVPCRGSDAGRRLVENPEVDIVILTGGTETAESMLRIRPDLALAAETGGKNATIVTGLADRELAIKHALQSAFGHSGQKCSATSLLLLEEEVFEDESFREMLADACKSMIVGSPWELQTRVGPLIRPPSGELARGLKELEPGESWLVMPEPCDDNPNLYRPGIKWNVQPGSFTHMTELFGPVLGVMPFRKLEQAIRIVNATGFGLTSGLESLDDREQELWREQIQAGNLYINRSTTGAIVLRQPFGGLGKSAFGPGIKAGGPHYVASLMKLRDQIDHPQMFNAHRFELPALQSMRENLKSPEAAALIERCGGEDATESVIDRLQTALASYDHWATEEYRQQHDSVRLVGQDNWRRYCPIPALRIGISAADGPLDIVRCIAAAHAAGCRITLSHRPAEALALVELVEFLTADWAARIEMIEETTQQWIDAIEEGEVLRIRMTPAAMVDPAVREAANQHNVYICQTPVLSDGRYELLHYVREQSICVDYHRYGNLGRRSEEPRRHVL
>NZ_CP036292.1|WP_145123616.1|6719416_6720082_-|NUDIX-domain-containing-protein
MPTNQPVELPLPVQPMTRLGEQRSRTRSAYNQASVGLAYGRHAGPVPGDARQAAVLIMLAWDGAQWNLPLTKRPTSLRHHGGQICFPGGRLEAGESAVEAAVREFDEELGMVPDDLQILGRLSTMHVYASHNVVTPIVATTRQTMQFRLDPVEVAQAIMLPWDALTDESRWTMRSMRRPISRNREVVDSFTFRYRALQFGEHLIWGATAMMLAELCQVGYR
>NZ_CP036292.1|WP_145123615.1|6718112_6719297_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MFETIQTAPPDSILGLTEAFQKDANPAKINLSVGVYKDTSGQTPVLRCVKQAEETLLKTETTKGYLGIDGLPEYRQHVHGLVFGDQVPASRVAVVQTPGGTGALRVAADLIAGQLKPAQIWLSNPTWANHNAIFTAAGVGVQTYSYLNAEKTGLDFDAMLEDLKTKPRTGDVVLLHACCHNPTGVDPTAEQWAQIAEVVRERGLLPLVDFAYQGFGQGITEDAVGIRTLLTTCDEMLVASSFSKNFGLYSERIGSLSLVAKKPEEATAGLSQLKRVVRTNYSNPPRHGGAIVSTVLSSPELTTLWHEEVAEMRNRIAAMRSQFVTQMHQRQSRRDFSFLLSQSGMFSFSGLNPMQVDQLRNEYAIYIVGSGRINVAGMTDENLPRLCDAVAAVL
>NZ_CP036292.1|WP_145123614.1|6717705_6718008_+|DUF167-domain-containing-protein
MIETTPRENQLIFAIHVSAGSRRNEVGGQHDGALRVAVTQAPEKGKANAAIIKLLAKTLGISKSQLEIISGDTHRRKTIAATQIDPQQIDQQLQTLATIK
>NZ_CP036292.1|WP_145123613.1|6717111_6717696_+|3-isopropylmalate-dehydratase-small-subunit
MQKFTKHTGLVATMDRANVDTDQIIPKQFLKRIERTGFGQFLFFDWRFNEDGSDNPDFELNQPAVKDASVLVTRRNFGNGSSREHAVWALDDYGFRAVLAPSFADIFFNNCFKNGVLPIVLSEEDIEELFRRTEQTEGYQLTVDLENNTISDGQGFDRTFEVEPSRRHNMLNGLDDIAMTLEHEAKISAYEAAL
>NZ_CP036292.1|WP_145123622.1|6732368_6734174_-|hypothetical-protein
MQSPRRPQAVAFRKLFPCGTLLVAWMLCSPSLAVAWQPSSPKFEQRDPDAVHFRKHLDRIAQAADPADAEAIAGWMLPHRDDQQVVYFLSSEPPTPSPLTTLRQKRAENLLRHAAAAAEADDLQLGYQMFWQAAREDPRNPSVLRALGLPADGEVPITVRPGRNADRQLDWPARSYLQVLTPHFMIDARCDREQAIELAQRLERVYWIWTQVFYPLWENRGSIQQTLRGQGRFESRISRHRVVLFANRQEYIDTLSKETPGIERSTGFYSNHAKITFLYAGADADLKTQYHELTHQLIGEASRMRVSPHVGLPSDFWVVEGIASYMESLYLHDSYATVGGWESSRLQFARYRVRGLGESMPLQRLVGLGRDAVQQSPDIASWYSYAAAYSHLLMDGPHREAFLEYVRSVYEQPAKSRSLPDVDLADFLNVTSDDVRLLRPGTQLQELCLTNTQVDETAAAALADQQHLTWLDLSRLPLTDAVLAALVRSNPNLDQLSLERTAASDATLAAIPGLLALEELDLTLAPVTDGHIAALAGLEKLETLWLTATQITDASVDVIAQLPSLRQVDMQRTAVTPAAIESLRTARPELTINPLQIVAAP
>NZ_CP036292.1|WP_145123623.1|6734270_6735827_-|altronate-dehydratase
MNKVSFVQLSPSDNVVVAISELAPGHILEVGGESVATINRIPAGHKVAVRSIQQGEAVYKFGSQIGSATADVAAGEHVHSHNLQHKHDVITEVPSTDPPAAPAKLERTFEGYVRPSGRVGTRNYIAVISTVNCSASVSQFVARRFEGDALDEYPNVDGVFAVTHETGCGMGYATLRHEMLSRVLVGAARHPNVAACVLIGLGCEQGSMGYLFEKHGIVPLHAPDGEKLTRDKGDAIPVLTMQDEGGTRKTIERAVEIVKDLLPVVNANRRETVSASELSVGLECGGSDGYSGITANPAVGCAADRIVASGGTAMLAETSEIYGAEHLLVQRSRSPEVALALIERIEWWKEYVGMFGLELDNNPSVGNKAGGLTTIAEKSLGAVAKAGSTALEAVYQYAEQVHQKGLVVMDTPGFDPASVTGMVAGGANMILFTTGRGSCFGCKPTPSIKIATNTAMYDRMIEDMDLNAGTVVEGSTVDQVGEEIYNKILAVASGEKTKSELAGIGDYEFIPWTVGPTL
>NZ_CP036292.1|WP_145123624.1|6736331_6739631_+|hypothetical-protein
MPLLRHSIHPEYAAQSLERRVPQLHHSLLSYLTLRTDREIPGLRGVVVRSVASHAARRLADPQSDPLASEKQITLLSGSLLALIAMLAIYAIASPKNTVQSVQRLMMPLASIEAPTSVRIGAVTPGDTQVAEGTSLTITAEIDGLKPDQQAWVETTQGSIAHREVMQATETEFTATVGASGDGIRHDTQYWIVAGDARRGPFEIKVEAVPIVSIGSVQYQPAAYTRLPSRSNNRGAIDGLEGTAVTVVAQSNLPIAKAKIEFNPKRIGSIWQATGGVKAMEIADDQMSMSTSWVLRRAEEERGVVAIESYRIIVEDAQGLTNAAPVIYPVKVAADLSPEVSIIVPHQSPKDLPIGMEQLIEVHALDPDFGLSRMEFEIRKGDRVLGTRKIFESTEALIGQQVSISAFRSEDWNLIAGDKVTVRCRAFDNRDMPGNQTTDPNSTVSEPIELHIVAPPEDAEDEADGDGLQKKSDRESDDPSGSGKQDGEGGGSGGQGDSTGEQAEGKGKGESGGGEAGGENQEPSEDSESGSDGAGGKPSDKPSEEGTEPNQGGGDAAGDSENKGSSKPGDSPAGDDPSQSKSDPSASEMTQESGPESGGKPGDQAGSPDASASRSESGEEPGQGEATDAEADGSEPPAGIAGDSKSGGAGSQRDAGEDAEKPQDDGPLHDGEIMERIREHMQKQQAEQEQGSQKPSDQESDDSGDGKPEQGADGAEGAGGKEDKQPQPADAKPAGDAASKGEPGGPGNQGEGAKPNQGNDSGQMPQDGTKPKPNGGNNNPDTGNNGKSDKGDQGSGEGKSPDDKPSATDPATDGNNDAGDTAGQEAENQTGSDGKPTGDDQAKGKSGDPAGSDAGDGTDAGQQDDAGADPNSDSKPSQGQGDQKGKGKGEASDPADQTDTPSGDDAGESGDDSMTAESKAGSSDSKSNPQGKPGKRPDGKQGEPGKSADAPPSEAAAQGDQMGDGAGADAHLPPEKINQEYAKKATDLVLDYLKKKQSEPDAELLDKLNWTEQDLQNFLNRWQQAQEMGRVGDEKAKQEYLEQIESLGIRPPASGKSRQTIQREDSLRDVRESGQRVAPPALYRDAFEAFRRSISRGNN
>NZ_CP036292.1|WP_145123625.1|6739707_6740949_+|hypothetical-protein
MSTRCLTTCILLAILCNNRPVVAQEGSFLDAIRQRIQSAADNQTEEEKEQTRKKLESLFSIVTEGAREIYRTLPDDSQKAIDQRRQAWMDAMASGVDDLTGDDIERWLDNSDNVILRSLSRGGDAPSVNAQSRTDLLPEQWWYGKQNRTLAQLLTQPPETIIRREDLPGPPIWFVNGITTKKAEAIVMADEIAEQLGRRVHLLHNPTFMEPPNHSGLDVEGYGTDDLSECLHDRLWPATVFNKLNRMDAEQLQAMLDDGQTLQGNPTTRQLAYVLLTAREPISLITHSQGCIIARNAMYTMAMLGRREQAEQQIAWIAAGIPLNDKELSPLPLQTTILDVGDDPIAKIVGMRGGSREYRGTDHSFSDHYCQQIQAEQLWHDALPATDKPAIPPAPESSTETKPDAKSPKRVKL
>NZ_CP036292.1|WP_145123626.1|6741371_6742379_-|ATP-binding-cassette-domain-containing-protein
MAGLAIRKLCKSFAGRIVLDHLELSVDPGQLVVLLGASGSGKTTLLRLIAGLETPDAGGIAIGGREVGRLSPRQRNVSMVFQDFALYPHMSVGDNIAFPLRGRKVSRAQVVSKVADVAGKLGLGALLDRRPDQISGGQQQRLAVARALVRDSQLLLMDEPLSNVDVRRRDAMRYELRSLQKEFALTVLYVTHDQTEAMLLGDQIAVIDRGVIQQMAPPDVIYDQPANRFVAQFIGSPPMNFIPDGRAGLLGIRPEDLSFRSAGDDDLKIDGVVDAVQCLGSHNVVHLRTDEGPVAVIVDRQQRVELGEQLTACAARCRLHRFAPSDGARLASPLV
>NZ_CP036292.1|WP_145123627.1|6742480_6743083_+|peptide-methionine-(R)-S-oxide-reductase-MsrB
MIVSKNHWRWVTGTTTVAITLWTLSMGNLTSRADDGQSKAPASATESSDSKWGPNAPPYTPKTKRELRKTLTRMQYSVTQQADTERAFSGPYWDSKQDGIYTCVVCGLPLFDSSTKFKSGTGWPSYWQPIREGNVGTKTDWKMLYPRTEVHCKRCKAHLGHVFNDGPQPTGLRFCMNGAALKFRERSSLEEPTAEPQSDR
>NZ_CP036292.1|WP_145123628.1|6743277_6744003_+|hypothetical-protein
MVVHSFTIAARNCCLLAAVVTSTAGAAGPFRMLVQEAPETKAPLSDGAKVPATPLPADLRTEAERIKNVKELAGDSIFGENRFPKVEGNQLRLPSLVAPTTQQVDIGNGQTPKNNADLVMTNTIPLPEGYDRSGNWVYSQYDWQAANTFSHPLYFQDAMLERNGHELKYCLQPALSAARFFTTIPALPYLMTIQRPCEYNHTLGYYRPGTRAPNLLQRPPYQRDAVLNQAAWTTGAVFLIP
>NZ_CP036292.1|WP_145123629.1|6744156_6744720_+|hypothetical-protein
MFYILFLIATATRLMPHPPNLVCVGAIGLFAGCYLRGRTAWLLPIGAMLASDVIGHVLRLPGMGFYNPAVFCMVYAGIAASALIGRGLAKNRTAARIGGAAVASSIVFFLASNLGVWFAGQYPPTVAGLIACYTMAIPFLTNTLIGNLLYSAVLFGTYEFSQSQWPARLTRLVSKQPAMQPAFARKS
>NZ_CP036292.1|WP_145123630.1|6745028_6745298_+|30S-ribosomal-protein-S15
MTITIERKAELIEEHKHSAGDNGSSEVQIAILTERINGLTDHMRTHKKDYASRRGLLGLVSRRRRLLDYLRNTDPQRYIEIIARLGIRK
>NZ_CP036292.1|WP_145123631.1|6745615_6747856_+|polyribonucleotide-nucleotidyltransferase
MNKFRVEKKIGKNTLILESGQLAKQAAGCVTIQYGETVVLTAAATSAPRPGLDFFPLTCDYRERMAAAGKFPGGFLKREGRPTMKETLTARLTDRPIRPLWPKGYKEEVQVQSFVLSSDGQNDGDVLAMNGAGCALLISPLPFQGPVASVRVGKIDGELVAFPTVDDLDESELDLIVSGTQDAVTMIEGFAQEMPEDEMVDAILFAHGVIREIIALQQELYDLVKPEKIEYTPPEDDGLFDRLKSAYYQEFKSLKQTAGKQDRAEACKALKERAKAEIIPDPNAEGAVCPNRFSHEWHELDSLIVRELILAGTRPDGRDHASLRPIYCETDLLPRTHGSSLFQRGETQALITVTLGTKRDEQRVDGLHDEFSKKFMLDYNFPSFSVGECRPIRGPGRREIGHGALAERSIAPVLPDADTFPYTIRVISDILESNGSSSMASVCGATLGLMAAGVPITNPVAGISVGLVKENDKWVLITDILGDEDHFGDMDFKISGTQNGITGIQLDLKIWGISEDIIRATLKQSREARIEILRKMLTTISRPRREIAATAPRLLRTKIEPAKIGMLIGPGGKNIRGIQESTGTVVEVDDDGNVLVASDNLESAQEAMKLIEACTATVQIGKIYDGTVSSIKDFGAFVEILPGRDGLVHISELSSGFISAIDSVVKVGDPMKVLVIDIDEHDRVKLSRRQAIDELGIEDEMASAVEEGGEDRGGSRDGGDDDRPRSRGRRSGGGGGGGRGRGPRRD

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Crispr_ID: NZ_CP036292_28

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_28

6740966-6741117

Orphan

Consensus_repeat	Method
CTTCGTTTCACCGCGGCGGCAACGCCCCGCGCGTCATACATTCTCGAGACTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_28

>merge|NZ_CP036292|28|6740966-6741117|CRISPRCasFinder
CTTCGTTTCACCGCGGCGGCAACGCCCCGCGCGTCATACATTCTCGAGACTCACACGCAAAGCGCGGCCCGATGGGCACGCGGTTAAACGATCTGCACCACTTCGTTTCACCGCGGCGGCAACGCCCCGCGCGTCACACATTCTCGAGACTC

>NZ_CP036292|28|27|6740966-6741117|CRISPRCasFinder
CTTCGTTTCACCGCGGCGGCAACGCCCCGCGCGTCATACATTCTCGAGACTC	ACACGCAAAGCGCGGCCCGATGGGCACGCGGTTAAACGATCTGCACCA
CTTCGTTTCACCGCGGCGGCAACGCCCCGCGCGTCACACATTCTCGAGACTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123624.1\|6736331_6739631_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273344
NZ_CP036292.1\|WP_145123629.1\|6744156_6744720_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123635.1\|6752785_6753688_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123617.1\|6719982_6723840_+\|aldehyde-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|143443
NZ_CP036292.1\|WP_145123632.1\|6748393_6748750_+\|STAS/SEC14-domain-containing-protein	unknown	unknown	gnl\|CDD\|378774
NZ_CP036292.1\|WP_145123631.1\|6745615_6747856_+\|polyribonucleotide-nucleotidyltransferase	unknown	unknown	gnl\|CDD\|236995
NZ_CP036292.1\|WP_145123627.1\|6742480_6743083_+\|peptide-methionine-(R)-S-oxide-reductase-MsrB	unknown	unknown	gnl\|CDD\|234692
NZ_CP036292.1\|WP_145123630.1\|6745028_6745298_+\|30S-ribosomal-protein-S15	unknown	unknown	gnl\|CDD\|180170
NZ_CP036292.1\|WP_145123620.1\|6726069_6727512_+\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|379862
NZ_CP036292.1\|WP_145123618.1\|6724371_6725385_+\|dihydrofolate-reductase	unknown	unknown	gnl\|CDD\|238127
NZ_CP036292.1\|WP_145124318.1\|6731143_6731617_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|131643
NZ_CP036292.1\|WP_145123622.1\|6732368_6734174_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275381
NZ_CP036292.1\|WP_145123633.1\|6749038_6750190_-\|Fic-family-protein	unknown	unknown	gnl\|CDD\|225718
NZ_CP036292.1\|WP_145123621.1\|6727523_6731012_+\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	unknown	unknown	gnl\|CDD\|226220
NZ_CP036292.1\|WP_145123623.1\|6734270_6735827_-\|altronate-dehydratase	unknown	unknown	gnl\|CDD\|377287
NZ_CP036292.1\|WP_145123626.1\|6741371_6742379_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|226359
NZ_CP036292.1\|WP_145123619.1\|6725464_6725911_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|236558
NZ_CP036292.1\|WP_145123634.1\|6750649_6751906_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|214615
NZ_CP036292.1\|WP_145123625.1\|6739707_6740949_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123628.1\|6743277_6744003_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123624.1\|6736331_6739631_+\|hypothetical-protein	gnl\|CDD\|273344	TIGR00927, retinal_rod, K+-dependent Na+/Ca+ exchanger. [Transport and binding proteins, Cations and iron carrying compounds].	4.85301e-11
NZ_CP036292.1\|WP_145123633.1\|6749038_6750190_-\|Fic-family-protein	gnl\|CDD\|225718	COG3177, COG3177, Fic family protein [Function unknown].	3.14333e-40
NZ_CP036292.1\|WP_145123617.1\|6719982_6723840_+\|aldehyde-dehydrogenase-family-protein	gnl\|CDD\|143443	cd07125, ALDH_PutA-P5CDH, Delta(1)-pyrroline-5-carboxylate dehydrogenase, PutA. The proline catabolic enzymes of the aldehyde dehydrogenase (ALDH) protein superfamily, proline dehydrogenase and Delta(1)-pyrroline-5-carboxylate dehydrogenase (P5CDH, (EC=1.5.1.12 )), catalyze the two-step oxidation of proline to glutamate; P5CDH catalyzes the oxidation of glutamate semialdehyde, utilizing NAD+ as the electron acceptor. In some bacteria, the two enzymes are fused into the bifunctional flavoenzyme, proline utilization A (PutA) These enzymes play important roles in cellular redox control, superoxide generation, and apoptosis. In certain prokaryotes such as Escherichia coli, PutA is also a transcriptional repressor of the proline utilization genes.	0
NZ_CP036292.1\|WP_145123632.1\|6748393_6748750_+\|STAS/SEC14-domain-containing-protein	gnl\|CDD\|378774	pfam11964, SpoIIAA-like, SpoIIAA-like. These proteins adopt an alpha/beta SpoIIAA-like fold, similar to that found in STAT (pfam01740). They adopt open and closed conformations arising from different arrangements of their alpha-2 and alpha-3 helices. They may be membrane associated and may function as carriers of non-polar compounds.	8.21623e-29
NZ_CP036292.1\|WP_145123631.1\|6745615_6747856_+\|polyribonucleotide-nucleotidyltransferase	gnl\|CDD\|236995	PRK11824, PRK11824, polynucleotide phosphorylase/polyadenylase; Provisional.	0
NZ_CP036292.1\|WP_145123627.1\|6742480_6743083_+\|peptide-methionine-(R)-S-oxide-reductase-MsrB	gnl\|CDD\|234692	PRK00222, PRK00222, peptide-methionine (R)-S-oxide reductase MsrB.	4.6983e-79
NZ_CP036292.1\|WP_145123630.1\|6745028_6745298_+\|30S-ribosomal-protein-S15	gnl\|CDD\|180170	PRK05626, rpsO, 30S ribosomal protein S15; Reviewed.	2.11438e-46
NZ_CP036292.1\|WP_145123620.1\|6726069_6727512_+\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	gnl\|CDD\|379862	pfam16576, HlyD_D23, Barrel-sandwich domain of CusB or HlyD membrane-fusion. HlyD_D23 is the combined domains 2 and 3 of the membrane-fusion proteins CusB and HlyD, which forms a barrel-sandwich. CusB and HlyD proteins are membrane fusion proteins of the CusCFBA copper efflux system in E.coli and related bacteria. The whole molecule hinges between D2 and D3. Efflux systems of this resistance-nodulation-division group - RND - have been developed to excrete poisonous metal ions, and in E.coli the only one that deals with silver and copper is the CusA transporter. The transporter CusA works in conjunction with a periplasmic component that is a membrane fusion protein, eg CusB, and an outer-membrane channel component CusC in a CusABC complex driven by import of protons.	9.25873e-09
NZ_CP036292.1\|WP_145123618.1\|6724371_6725385_+\|dihydrofolate-reductase	gnl\|CDD\|238127	cd00209, DHFR, Dihydrofolate reductase (DHFR). Reduces 7,8-dihydrofolate to 5,6,7,8-tetrahydrofolate with NADPH as a cofactor. This is an essential step in the biosynthesis of deoxythymidine phosphate since 5,6,7,8-tetrahydrofolate is required to regenerate 5,10-methylenetetrahydrofolate which is then utilized by thymidylate synthase. Inhibition of DHFR interrupts thymidilate synthesis and DNA replication, inhibitors of DHFR (such as Methotrexate) are used in cancer chemotherapy. 5,6,7,8-tetrahydrofolate also is involved in glycine, serine, and threonine metabolism and aminoacyl-tRNA biosynthesis.	2.02193e-48
NZ_CP036292.1\|WP_145124318.1\|6731143_6731617_+\|hypothetical-protein	gnl\|CDD\|131643	TIGR02594, hypothetical_protein, TIGR02594 family protein. Members of this protein family known so far are restricted to the bacteria, and for the most to the proteobacteria. The function is unknown.	0.00849221
NZ_CP036292.1\|WP_145123622.1\|6732368_6734174_-\|hypothetical-protein	gnl\|CDD\|275381	sd00034, LRR_AMN1, leucine-rich repeats, antagonist of mitotic exit network protein 1-like subfamily. A leucine-rich repeat (LRR) is a structural protein motif of 20-30 amino acids that is unusually rich in the hydrophobic amino acid leucine. The conserved eleven-residue sequence motif (LxxLxLxxN/CxL) within the LRRs corresponds to the beta-strand and adjacent loop regions, whereas the remaining parts of the repeats are variable. LRRs fold together to form a solenoid protein domain, termed leucine-rich repeat domain. Leucine-rich repeats are usually involved in protein-protein interactions.	3.00576e-15
NZ_CP036292.1\|WP_145123621.1\|6727523_6731012_+\|CusA/CzcA-family-heavy-metal-efflux-RND-transporter	gnl\|CDD\|226220	COG3696, COG3696, Putative silver efflux pump [Inorganic ion transport and metabolism].	0
NZ_CP036292.1\|WP_145123623.1\|6734270_6735827_-\|altronate-dehydratase	gnl\|CDD\|377287	pfam04295, GD_AH_C, D-galactarate dehydratase / Altronate hydrolase, C-terminus. Family members include the C termini of D-galactarate dehydratase (EC:4.2.1.42) which is thought to catalyze the reaction D-galactarate = 5-keto-4-deoxy-D-glucarate + H2O, and altronate hydrolase (altronic acid hydratase, EC:4.2.1.7), which catalyzes D-altronate = 2-keto-2-deoxygluconate + H2O. As purified, both enzymes are catalytically inactive in the absence of added Fe2+, Mn2+, and beta-mercaptoethanol. Synergistic activation of altronate hydrolase activity is seen in the presence of both iron and manganese ions, suggesting that the enzyme may have two ion binding sites. Mn2+ appears to be part of the enzyme active centre, but the function of the single bound Fe2+ ion is unknown. The hydratase has no Fe-S core.	0
NZ_CP036292.1\|WP_145123626.1\|6741371_6742379_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|226359	COG3839, MalK, ABC-type sugar transport systems, ATPase components [Carbohydrate transport and metabolism].	4.06656e-135
NZ_CP036292.1\|WP_145123619.1\|6725464_6725911_+\|hypothetical-protein	gnl\|CDD\|236558	PRK09545, znuA, zinc ABC transporter substrate-binding protein ZnuA.	0.00796675
NZ_CP036292.1\|WP_145123634.1\|6750649_6751906_+\|hypothetical-protein	gnl\|CDD\|214615	smart00318, SNc, Staphylococcal nuclease homologues.	3.13945e-27

>NZ_CP036292.1|WP_145123625.1|6739707_6740949_+|hypothetical-protein
MSTRCLTTCILLAILCNNRPVVAQEGSFLDAIRQRIQSAADNQTEEEKEQTRKKLESLFSIVTEGAREIYRTLPDDSQKAIDQRRQAWMDAMASGVDDLTGDDIERWLDNSDNVILRSLSRGGDAPSVNAQSRTDLLPEQWWYGKQNRTLAQLLTQPPETIIRREDLPGPPIWFVNGITTKKAEAIVMADEIAEQLGRRVHLLHNPTFMEPPNHSGLDVEGYGTDDLSECLHDRLWPATVFNKLNRMDAEQLQAMLDDGQTLQGNPTTRQLAYVLLTAREPISLITHSQGCIIARNAMYTMAMLGRREQAEQQIAWIAAGIPLNDKELSPLPLQTTILDVGDDPIAKIVGMRGGSREYRGTDHSFSDHYCQQIQAEQLWHDALPATDKPAIPPAPESSTETKPDAKSPKRVKL
>NZ_CP036292.1|WP_145123624.1|6736331_6739631_+|hypothetical-protein
MPLLRHSIHPEYAAQSLERRVPQLHHSLLSYLTLRTDREIPGLRGVVVRSVASHAARRLADPQSDPLASEKQITLLSGSLLALIAMLAIYAIASPKNTVQSVQRLMMPLASIEAPTSVRIGAVTPGDTQVAEGTSLTITAEIDGLKPDQQAWVETTQGSIAHREVMQATETEFTATVGASGDGIRHDTQYWIVAGDARRGPFEIKVEAVPIVSIGSVQYQPAAYTRLPSRSNNRGAIDGLEGTAVTVVAQSNLPIAKAKIEFNPKRIGSIWQATGGVKAMEIADDQMSMSTSWVLRRAEEERGVVAIESYRIIVEDAQGLTNAAPVIYPVKVAADLSPEVSIIVPHQSPKDLPIGMEQLIEVHALDPDFGLSRMEFEIRKGDRVLGTRKIFESTEALIGQQVSISAFRSEDWNLIAGDKVTVRCRAFDNRDMPGNQTTDPNSTVSEPIELHIVAPPEDAEDEADGDGLQKKSDRESDDPSGSGKQDGEGGGSGGQGDSTGEQAEGKGKGESGGGEAGGENQEPSEDSESGSDGAGGKPSDKPSEEGTEPNQGGGDAAGDSENKGSSKPGDSPAGDDPSQSKSDPSASEMTQESGPESGGKPGDQAGSPDASASRSESGEEPGQGEATDAEADGSEPPAGIAGDSKSGGAGSQRDAGEDAEKPQDDGPLHDGEIMERIREHMQKQQAEQEQGSQKPSDQESDDSGDGKPEQGADGAEGAGGKEDKQPQPADAKPAGDAASKGEPGGPGNQGEGAKPNQGNDSGQMPQDGTKPKPNGGNNNPDTGNNGKSDKGDQGSGEGKSPDDKPSATDPATDGNNDAGDTAGQEAENQTGSDGKPTGDDQAKGKSGDPAGSDAGDGTDAGQQDDAGADPNSDSKPSQGQGDQKGKGKGEASDPADQTDTPSGDDAGESGDDSMTAESKAGSSDSKSNPQGKPGKRPDGKQGEPGKSADAPPSEAAAQGDQMGDGAGADAHLPPEKINQEYAKKATDLVLDYLKKKQSEPDAELLDKLNWTEQDLQNFLNRWQQAQEMGRVGDEKAKQEYLEQIESLGIRPPASGKSRQTIQREDSLRDVRESGQRVAPPALYRDAFEAFRRSISRGNN
>NZ_CP036292.1|WP_145123623.1|6734270_6735827_-|altronate-dehydratase
MNKVSFVQLSPSDNVVVAISELAPGHILEVGGESVATINRIPAGHKVAVRSIQQGEAVYKFGSQIGSATADVAAGEHVHSHNLQHKHDVITEVPSTDPPAAPAKLERTFEGYVRPSGRVGTRNYIAVISTVNCSASVSQFVARRFEGDALDEYPNVDGVFAVTHETGCGMGYATLRHEMLSRVLVGAARHPNVAACVLIGLGCEQGSMGYLFEKHGIVPLHAPDGEKLTRDKGDAIPVLTMQDEGGTRKTIERAVEIVKDLLPVVNANRRETVSASELSVGLECGGSDGYSGITANPAVGCAADRIVASGGTAMLAETSEIYGAEHLLVQRSRSPEVALALIERIEWWKEYVGMFGLELDNNPSVGNKAGGLTTIAEKSLGAVAKAGSTALEAVYQYAEQVHQKGLVVMDTPGFDPASVTGMVAGGANMILFTTGRGSCFGCKPTPSIKIATNTAMYDRMIEDMDLNAGTVVEGSTVDQVGEEIYNKILAVASGEKTKSELAGIGDYEFIPWTVGPTL
>NZ_CP036292.1|WP_145123622.1|6732368_6734174_-|hypothetical-protein
MQSPRRPQAVAFRKLFPCGTLLVAWMLCSPSLAVAWQPSSPKFEQRDPDAVHFRKHLDRIAQAADPADAEAIAGWMLPHRDDQQVVYFLSSEPPTPSPLTTLRQKRAENLLRHAAAAAEADDLQLGYQMFWQAAREDPRNPSVLRALGLPADGEVPITVRPGRNADRQLDWPARSYLQVLTPHFMIDARCDREQAIELAQRLERVYWIWTQVFYPLWENRGSIQQTLRGQGRFESRISRHRVVLFANRQEYIDTLSKETPGIERSTGFYSNHAKITFLYAGADADLKTQYHELTHQLIGEASRMRVSPHVGLPSDFWVVEGIASYMESLYLHDSYATVGGWESSRLQFARYRVRGLGESMPLQRLVGLGRDAVQQSPDIASWYSYAAAYSHLLMDGPHREAFLEYVRSVYEQPAKSRSLPDVDLADFLNVTSDDVRLLRPGTQLQELCLTNTQVDETAAAALADQQHLTWLDLSRLPLTDAVLAALVRSNPNLDQLSLERTAASDATLAAIPGLLALEELDLTLAPVTDGHIAALAGLEKLETLWLTATQITDASVDVIAQLPSLRQVDMQRTAVTPAAIESLRTARPELTINPLQIVAAP
>NZ_CP036292.1|WP_145124318.1|6731143_6731617_+|hypothetical-protein
MTGCNPADTPTDDATPTAESAADDHGHDHSGTDHSEVGHGHGVGPHDGTIADWGGGKFHVEFTVDHDKTEATVYVLGGDEKTAAPIAAESIELTIIDPEMQVTLKPSPQEGDPDGTASRFIGTHEKLGVVQEYAGTMTGVIDGTPYTGEFKEEAHTH
>NZ_CP036292.1|WP_145123621.1|6727523_6731012_+|CusA/CzcA-family-heavy-metal-efflux-RND-transporter
MLDAVIHFSLRYRMLVVVISLALLVYGSYQAAQMPIDVFPDLDRPRVVIITEAPGLATEEVETLVTQPIEIALIGANGVQAVRSQTTAGLNVIYIEFDWSTQIRAARQTVQERLTTLQGILPAGIRPQMTPPSSIMGQIVIAGIYRQPGPRGGKLAVVGKTSMMAERIDSADPAEAIQVWQPVERKDLKTWKRVETQSITWTAAAADDPQLAGESPEGVGIATIQIAGQEHDVNFYSDAKRQLDLRTVADWIIRPRLLKTTGVAEVFMQGGDRKQYQILIDPTALLEYDVTVQDVAQALRESNINTSGGFAVTGETERSIRILGRLGPESRVVIEDLKKIPVGYHPKRSVLLEQVARVSEGPQLKRGDGSVDGQPGIVFTTVKQPHVDTRQLTNDIAAAFAEVEASLPADIIINSELFRLKNFIDRGIFNVAEALVIGAFLVMVVLFLFLLNFRTTFITLTAIPLSLVITTLVFRWIGWFSGSELSINVMTLGGIAVAMGELVDDAIVDVENIFRRLKENNAAPTRRAAIQVVFEASKEIRSAIMFGTAVVILVFLPLFALSGVEGRLFAPLGLAYIISILASFLVSLTVTPALSYYLLPKSSATHRDHDGLLLRGLKRATTPWIQLSMAWPRMLLCATWLGVLLAAWQMAQLGRNFLPPFDEGSVQVNVTLPPGSSLETSNRVSQTIDAVFQSMQKNEDRPEGEILHFVRRTGRAELDEHASPVNVGEYILSMNPEVDQDREEILAGLLKKLKDEAPGVDIEVEQPLAHLISHMVSGIYAQIAIKIHGDDLDTLQRIAEQVKSTLQSIPGITPPVVEPIQQVPELHIQLRSDDLALHGLTRQYVADVLQIALQGEVVSQVLEGQRRFDLMVRLEEAYRTDYANLGRLRIDLPDHPGYADRGQIELQEIANIGEGSGPNSVNREDARRRIAVRCNTQGRDLASAVGEIKQRIDRQIQLPIGYYIEYGGQFESQQRATQWIIALAGVSVVGMFVVLMLLFPSVRIVLQILNALPTAFIGGVLALVITDQSLTVASLVGFISLGGIAVRNGILLVTHYFHLMKEEGESFTQAMVLRGSLERLAPVLMTALTAGIGLIPLVLGGQEPGREILYPVATVILGGLTTSTFCEFLIHPGLFWAFSGKDAAALASGTAEDVDSQFEPPT
>NZ_CP036292.1|WP_145123620.1|6726069_6727512_+|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MQHVPSLTKLLFGLALAAGVALTTWYFRDVLPFAGSVPAVAKEDPPQPASEKQTILEISVQARKNLGLTSQPARPQTYWRSLQIPGKLADRPGVSDRGVTSPAESVVTEIHISPGDAIRPGERLFTLRLFSEYLQATQTQLFKAKQETSIIQADIDRVSDAVTSGAVVRSKMIELQGNLRRQQILIEAARQDLRSRGLDSAQIEQIESGRFLSTIDVRAPEALPTVPLTETNTDRAARTIQPVQQARFDSSSSRAPEFAFEVQELLVELGQQVQAGQPLATLANHQALYVVGHAFKREAPFLEQAAQEGRAIDIEFADDATDQWPELEQRFEIRHLSNAIDTNSRTFDFFIPLRNQSRAYQKAEQTFLVWRFRPGQRVRLHVPVEKLENVLVLPAAAVVRDGPEAYVFMQNGDLFKRLPVHVLHEDRQSIVLANDGSVTPGTYLAQNAAASLNRVLRSQAASGQQVGVHVHPDGTVHAAH
>NZ_CP036292.1|WP_145123619.1|6725464_6725911_+|hypothetical-protein
MRPLLSLLLIATFMLGHVVPHSHAASGGAEPGDHAHRPHVHLSHGHDHDHGHHHGQADRPSAGEESPADALTELSLACDHDGDAVYFVDSDWTVARNAVSISLDLSSLPFTSIAGTIPQRERQYRRSSGPPDRRPKLPIYLLTASLRL
>NZ_CP036292.1|WP_145123618.1|6724371_6725385_+|dihydrofolate-reductase
MRVQDDRCRNAQERTVRDAANVCKTLCQGRVRRSDGGLLRRRRLPNRRGRFAARGEGEHDRFRETVPNAGAEVSWNRYPIDRCCVGRWQGQRNHDGGVYDQGGYDRRIEVLARTSSSFNLEEWQDHRPEVLLRPQFLNTLCPPMRLPIAFVAGEPLSPRLPRTCSQGKVWFCRFPKQGAPSGMIIISAMSEDRVIGSQNGMPWNVPAEYQQYLDFVAGQTVIMGRKTFEIFGKDVAPETSLIVVSRSAELDDVPVATTFDKAVAMAKALGKQIFIAGGSSIYEQAIAVADQMYLSTIHGQYSGDAYFPAFDADNWQVVETREQPQFTFRRWKRKTTS
>NZ_CP036292.1|WP_145123617.1|6719982_6723840_+|aldehyde-dehydrogenase-family-protein
MLGCKRSAFATVVPLSGSSVARAAAVRRVGLLASNNSKRRIDTVSSSASDPAAEESPFLNLNEAVAATESAASGLTGWQRDAARAIALAKQLLQRSQQLLTPAERRQQSELDRMIGHHEDKATLIEMTDQAFRTDVPQRVADQLTHILDVQGVPRFFSPLDRTLLRGFQTFGGYLPGVAVPMVKDKMRHETANVILPAEKEVLEKHLRERQREGIRMNVCLLGEALLGEGETRQRLKKYLAALQMPEIECISVKVSTIYSQISTLARSHTESVIADRLELLYRAAMRQTFQRRDGTQTSKFVYLDMEEYRDLHLTVDVLKRTLDRPELSQVRAGIALQSYIPDSFDVLQDLAQWAQRRTAAGGLPLTIRVVKGANMEMERVEASIEGWPQAPYTTKHETDANYKRMIRTILAPENSTALRLGVASHNLFDIALVAIWASEADALQRVQFEMLEGMANQQRRALFEMTGSMLLYAPACEQTDFLNAIGYLIRRLDENTGQENFLRHAFQLQPGTETWRTLADGFRASLVAIDSVTTKPRRQQDRSQVPERPEVGETWQQFINEPNTDWSLPQNSRWAQELLASWRDRCDDAATRIPLSIAGREVTDAREIAESRDPSRPGKIACRYAMATSDDIDAAIACARQDPRNWRSMPSEARRATLHDAAQLLRQRRGDLLAAALIDGGKTLAESDPEVSEAIDFIEFYSLCADQAYQSPQIQASGVGVVAVISPWNFPIAIPCGGVAAALAAGNTVLLKPASETVLPAYLLCQAFWDAGVPREALQLVPCRGSDAGRRLVENPEVDIVILTGGTETAESMLRIRPDLALAAETGGKNATIVTGLADRELAIKHALQSAFGHSGQKCSATSLLLLEEEVFEDESFREMLADACKSMIVGSPWELQTRVGPLIRPPSGELARGLKELEPGESWLVMPEPCDDNPNLYRPGIKWNVQPGSFTHMTELFGPVLGVMPFRKLEQAIRIVNATGFGLTSGLESLDDREQELWREQIQAGNLYINRSTTGAIVLRQPFGGLGKSAFGPGIKAGGPHYVASLMKLRDQIDHPQMFNAHRFELPALQSMRENLKSPEAAALIERCGGEDATESVIDRLQTALASYDHWATEEYRQQHDSVRLVGQDNWRRYCPIPALRIGISAADGPLDIVRCIAAAHAAGCRITLSHRPAEALALVELVEFLTADWAARIEMIEETTQQWIDAIEEGEVLRIRMTPAAMVDPAVREAANQHNVYICQTPVLSDGRYELLHYVREQSICVDYHRYGNLGRRSEEPRRHVL
>NZ_CP036292.1|WP_145123626.1|6741371_6742379_-|ATP-binding-cassette-domain-containing-protein
MAGLAIRKLCKSFAGRIVLDHLELSVDPGQLVVLLGASGSGKTTLLRLIAGLETPDAGGIAIGGREVGRLSPRQRNVSMVFQDFALYPHMSVGDNIAFPLRGRKVSRAQVVSKVADVAGKLGLGALLDRRPDQISGGQQQRLAVARALVRDSQLLLMDEPLSNVDVRRRDAMRYELRSLQKEFALTVLYVTHDQTEAMLLGDQIAVIDRGVIQQMAPPDVIYDQPANRFVAQFIGSPPMNFIPDGRAGLLGIRPEDLSFRSAGDDDLKIDGVVDAVQCLGSHNVVHLRTDEGPVAVIVDRQQRVELGEQLTACAARCRLHRFAPSDGARLASPLV
>NZ_CP036292.1|WP_145123627.1|6742480_6743083_+|peptide-methionine-(R)-S-oxide-reductase-MsrB
MIVSKNHWRWVTGTTTVAITLWTLSMGNLTSRADDGQSKAPASATESSDSKWGPNAPPYTPKTKRELRKTLTRMQYSVTQQADTERAFSGPYWDSKQDGIYTCVVCGLPLFDSSTKFKSGTGWPSYWQPIREGNVGTKTDWKMLYPRTEVHCKRCKAHLGHVFNDGPQPTGLRFCMNGAALKFRERSSLEEPTAEPQSDR
>NZ_CP036292.1|WP_145123628.1|6743277_6744003_+|hypothetical-protein
MVVHSFTIAARNCCLLAAVVTSTAGAAGPFRMLVQEAPETKAPLSDGAKVPATPLPADLRTEAERIKNVKELAGDSIFGENRFPKVEGNQLRLPSLVAPTTQQVDIGNGQTPKNNADLVMTNTIPLPEGYDRSGNWVYSQYDWQAANTFSHPLYFQDAMLERNGHELKYCLQPALSAARFFTTIPALPYLMTIQRPCEYNHTLGYYRPGTRAPNLLQRPPYQRDAVLNQAAWTTGAVFLIP
>NZ_CP036292.1|WP_145123629.1|6744156_6744720_+|hypothetical-protein
MFYILFLIATATRLMPHPPNLVCVGAIGLFAGCYLRGRTAWLLPIGAMLASDVIGHVLRLPGMGFYNPAVFCMVYAGIAASALIGRGLAKNRTAARIGGAAVASSIVFFLASNLGVWFAGQYPPTVAGLIACYTMAIPFLTNTLIGNLLYSAVLFGTYEFSQSQWPARLTRLVSKQPAMQPAFARKS
>NZ_CP036292.1|WP_145123630.1|6745028_6745298_+|30S-ribosomal-protein-S15
MTITIERKAELIEEHKHSAGDNGSSEVQIAILTERINGLTDHMRTHKKDYASRRGLLGLVSRRRRLLDYLRNTDPQRYIEIIARLGIRK
>NZ_CP036292.1|WP_145123631.1|6745615_6747856_+|polyribonucleotide-nucleotidyltransferase
MNKFRVEKKIGKNTLILESGQLAKQAAGCVTIQYGETVVLTAAATSAPRPGLDFFPLTCDYRERMAAAGKFPGGFLKREGRPTMKETLTARLTDRPIRPLWPKGYKEEVQVQSFVLSSDGQNDGDVLAMNGAGCALLISPLPFQGPVASVRVGKIDGELVAFPTVDDLDESELDLIVSGTQDAVTMIEGFAQEMPEDEMVDAILFAHGVIREIIALQQELYDLVKPEKIEYTPPEDDGLFDRLKSAYYQEFKSLKQTAGKQDRAEACKALKERAKAEIIPDPNAEGAVCPNRFSHEWHELDSLIVRELILAGTRPDGRDHASLRPIYCETDLLPRTHGSSLFQRGETQALITVTLGTKRDEQRVDGLHDEFSKKFMLDYNFPSFSVGECRPIRGPGRREIGHGALAERSIAPVLPDADTFPYTIRVISDILESNGSSSMASVCGATLGLMAAGVPITNPVAGISVGLVKENDKWVLITDILGDEDHFGDMDFKISGTQNGITGIQLDLKIWGISEDIIRATLKQSREARIEILRKMLTTISRPRREIAATAPRLLRTKIEPAKIGMLIGPGGKNIRGIQESTGTVVEVDDDGNVLVASDNLESAQEAMKLIEACTATVQIGKIYDGTVSSIKDFGAFVEILPGRDGLVHISELSSGFISAIDSVVKVGDPMKVLVIDIDEHDRVKLSRRQAIDELGIEDEMASAVEEGGEDRGGSRDGGDDDRPRSRGRRSGGGGGGGRGRGPRRD
>NZ_CP036292.1|WP_145123632.1|6748393_6748750_+|STAS/SEC14-domain-containing-protein
MAIVLHEDFDTGLLEVKVSDKLSKEDYEHFEPAVERLIESCGKIKILLEMHDFHGWEMGAVWEDIKFATKHCRDIEKIAMVGETKWEKWMSAICKPFTMSTIKYFDAGQDQEARQWLA
>NZ_CP036292.1|WP_145123633.1|6749038_6750190_-|Fic-family-protein
MVKKSLFSEVSPGAIVSIAGNEIAFVPDSLPPGWEFPGRLWPLLAEAKSQIGILEGIGRVLPNPGILLRPLEDREAIRSSRLEGTYATPQELLLFELEPRVPTSDRDPRNDHREVFNYRRALHLGVNDSRPLCLRLLRDMHRILLGGVRGRDKNPGNFRNCQVAIGGSRRFVPPPPESVMGCLYEMESYFHVEDSRYDPLVNCFLMHYQFETIHPFNDGNGRIGRLLLAIMMQQKCAMTKPWLYLSEFFEQHRDEYIDRLFQVSTQAKWSAWVEFCLHATVAQAKATITRCERLLAIREDFNGRLNKVGGNVRLYTIMEEIFRSPFIRVSDVPELLGISYPTAKSDMERLADAGILKELSGVSPKTYYAPEVFSVAYDELPDS
>NZ_CP036292.1|WP_145123634.1|6750649_6751906_+|hypothetical-protein
MKLRFRRSIKPPFGRFTVTNRNITQSFRTPIGTFSNPLFSSSRSRKGTANGGSSLGCLGGLAVCLFAACCGFWGLLEFISPAATSRTNNAPATSIEVVDSDAAKEATSTARNLTPAPAESPDATDALQTPTATSAQESPPSTIASTVPDKPKQSRLPRPRLRTWTTKGGSNTVNATLTNFNETHVQLLRADNGTRVAVPINLLCLADQQYVDAISAPPHSENAILHVGTVHRVKDGDTVDFHSVNGEQFTLRLEGVDAPESTQQFGPEATRWLTNHVDGKLLRAEVTGQDRYGRALGNLYISKDWVNESLVSAGYAWHYVEYNKDIRLANAQNAARGLAKGLWRDAKRVTPWDYRNGQRIATALPANVPSTRENEVTVFVTDTGTKYHRAGCRHLRKSKYAMPLSRARSAYEPCRVCH
>NZ_CP036292.1|WP_145123635.1|6752785_6753688_+|hypothetical-protein
MSVADPSSHSKEHPQRSLRISQFDQVSSMLMALLVFVGFFVFFMFMIWLLDRLNFRTGEVVVAIVEEAAGRGENAEGFERDFEPPGEEEVSELTEPTLTDTLQAVTDAVSSVAASLDSMNTDASASTTGSGQGDSRPPGPEGEGEDIIPRFERWNLKFQAKSMVAYAEQLDFYQIELGAIGGSTEGVDYASNLAKSPKKKHNPDTSTEKRLYFRFTQAGPLERWDKSLLGKAGVGVGAGRHVLKFIPPNLENILAHTELEYAKEKGYQSVTQIAKTIFESQPGGDGHHFVVIEQRYRKPK

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Crispr_ID: NZ_CP036292_29

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_29

6812707-6812852

Orphan

Consensus_repeat	Method
CCCGGACGCGCGGGGCGATGCCCACGCGGTTAAACGAGAGAGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_29

>merge|NZ_CP036292|29|6812707-6812852|CRISPRCasFinder
CCCGGACGCGCGGGGCGATGCCCACGCGGTTAAACGAGAGAGGGGCCGCGAGATTTTTTAACCGCGAGCACAGCGGGCCGCGCGCGAATGCTGGTTCGAGTACCCGGACGCGCGGGGCGATGCCCACGCGGTTAAACGAGAGAGGG

>NZ_CP036292|29|28|6812707-6812852|CRISPRCasFinder
CCCGGACGCGCGGGGCGATGCCCACGCGGTTAAACGAGAGAGGG	GCCGCGAGATTTTTTAACCGCGAGCACAGCGGGCCGCGCGCGAATGCTGGTTCGAGTA
CCCGGACGCGCGGGGCGATGCCCACGCGGTTAAACGAGAGAGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123672.1\|6822745_6823660_+\|DUF1571-domain-containing-protein	unknown	unknown	gnl\|CDD\|377879
NZ_CP036292.1\|WP_145123659.1\|6803379_6805275_+\|efflux-transporter-outer-membrane-subunit	unknown	unknown	gnl\|CDD\|224455
NZ_CP036292.1\|WP_145123668.1\|6816481_6816766_+\|DUF2442-domain-containing-protein	unknown	unknown	gnl\|CDD\|378424
NZ_CP036292.1\|WP_145123671.1\|6822001_6822613_-\|thymidine-kinase	unknown	unknown	gnl\|CDD\|235272
NZ_CP036292.1\|WP_145123667.1\|6816264_6816501_+\|DUF4160-domain-containing-protein	unknown	unknown	gnl\|CDD\|379344
NZ_CP036292.1\|WP_145123657.1\|6798444_6801549_-\|MMPL-family-transporter	unknown	unknown	gnl\|CDD\|223911
NZ_CP036292.1\|WP_145123661.1\|6806576_6806861_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123666.1\|6814031_6816227_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145124322.1\|6819009_6819810_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123664.1\|6811777_6812386_+\|peptidase	unknown	unknown	gnl\|CDD\|374499
NZ_CP036292.1\|WP_145123660.1\|6805594_6806533_+\|DUF1559-domain-containing-protein	unknown	unknown	gnl\|CDD\|284919
NZ_CP036292.1\|WP_145117411.1\|6820482_6821907_+\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|373239
NZ_CP036292.1\|WP_145123665.1\|6812865_6813855_-\|dihydrodipicolinate-synthase-family-protein	unknown	unknown	gnl\|CDD\|188630
NZ_CP036292.1\|WP_145123662.1\|6806906_6810053_+\|DUF3386-family-protein	unknown	unknown	gnl\|CDD\|371771
NZ_CP036292.1\|WP_145123669.1\|6816983_6817979_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|100082
NZ_CP036292.1\|WP_145123655.1\|6790445_6791792_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|99747
NZ_CP036292.1\|WP_145123670.1\|6819972_6820287_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123656.1\|6791876_6798368_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|225858
NZ_CP036292.1\|WP_145123663.1\|6810205_6811696_+\|DUF2271-domain-containing-protein	unknown	unknown	gnl\|CDD\|224394
NZ_CP036292.1\|WP_145123658.1\|6801568_6803089_-\|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit	unknown	unknown	gnl\|CDD\|273776

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123672.1\|6822745_6823660_+\|DUF1571-domain-containing-protein	gnl\|CDD\|377879	pfam07608, DUF1571, Protein of unknown function (DUF1571). A family of paralogous proteins in Rhodopirellula baltica.	2.37743e-70
NZ_CP036292.1\|WP_145123659.1\|6803379_6805275_+\|efflux-transporter-outer-membrane-subunit	gnl\|CDD\|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	7.90807e-74
NZ_CP036292.1\|WP_145123668.1\|6816481_6816766_+\|DUF2442-domain-containing-protein	gnl\|CDD\|378424	pfam10387, DUF2442, Protein of unknown function (DUF2442). This family of bacterial and fungal proteins has several members annotated as being putative molybdopterin-guanine dinucleotide biosynthesis protein A; however this could not be verified. Hence the function is not known. This family also includes the DUF3532 that was found to be related and was merged into this family. Members of this family also fall into the NE0471 N-terminal domain-like superfamily, a family of proteins with a unique fold in SCOP:143880.	1.30152e-22
NZ_CP036292.1\|WP_145123667.1\|6816264_6816501_+\|DUF4160-domain-containing-protein	gnl\|CDD\|379344	pfam13711, DUF4160, Domain of unknown function (DUF4160).	4.52671e-19
NZ_CP036292.1\|WP_145123657.1\|6798444_6801549_-\|MMPL-family-transporter	gnl\|CDD\|223911	COG0841, AcrB, Cation/multidrug efflux pump [Defense mechanisms].	0
NZ_CP036292.1\|WP_145123671.1\|6822001_6822613_-\|thymidine-kinase	gnl\|CDD\|235272	PRK04296, PRK04296, thymidine kinase; Provisional.	4.16421e-111
NZ_CP036292.1\|WP_145123669.1\|6816983_6817979_+\|hypothetical-protein	gnl\|CDD\|100082	cd06161, S2P-M50_SpoIVFB, SpoIVFB Site-2 protease (S2P), a zinc metalloprotease (MEROPS family M50B), regulates intramembrane proteolysis (RIP), and is involved in the pro-sigmaK pathway of bacterial spore formation. SpoIVFB (sporulation protein, stage IV cell wall formation, F locus, promoter-distal B) is one of 4 proteins involved in endospore formation; the others are SpoIVFA (sporulation protein, stage IV cell wall formation, F locus, promoter-proximal A), BofA (bypass-of-forespore A), and SpoIVB (sporulation protein, stage IV cell wall formation, B locus). SpoIVFB is negatively regulated by SpoIVFA and BofA and activated by SpoIVB. It is thought that SpoIVFB, SpoIVFA, and BofA are located in the mother-cell membrane that surrounds the forespore and that SpoIVB is secreted from the forespore into the space between the two where it activates SpoIVFB.	7.76176e-07
NZ_CP036292.1\|WP_145123664.1\|6811777_6812386_+\|peptidase	gnl\|CDD\|374499	pfam16357, PepSY_TM_like_2, Putative PepSY_TM-like. This is a family of bacterial proteins with three PepSY-like TM regions.	2.61854e-44
NZ_CP036292.1\|WP_145123660.1\|6805594_6806533_+\|DUF1559-domain-containing-protein	gnl\|CDD\|284919	pfam07596, SBP_bac_10, Protein of unknown function (DUF1559). A large family of paralogous proteins apparently unique to planctomycetes.	6.19571e-50
NZ_CP036292.1\|WP_145117411.1\|6820482_6821907_+\|IS4-family-transposase	gnl\|CDD\|373239	pfam14706, Tnp_DNA_bind, Transposase DNA-binding. This domain occurs at the C-terminus of transposases including E. coli tnpA. TnpA encodes a transposase and an inhibitor protein, the inhibitor only differs from the transposase by the absence of the N-terminal 55 amino acids, which includes most of this domain. This domain consists of alpha helices and turns, and functions as a DNA-binding domain.	2.07371e-18
NZ_CP036292.1\|WP_145123665.1\|6812865_6813855_-\|dihydrodipicolinate-synthase-family-protein	gnl\|CDD\|188630	cd00408, DHDPS-like, Dihydrodipicolinate synthase family. Dihydrodipicolinate synthase family. A member of the class I aldolases, which use an active-site lysine which stabilizes a reaction intermediate via Schiff base formation, and have TIM beta/alpha barrel fold. The dihydrodipicolinate synthase family comprises several pyruvate-dependent class I aldolases that use the same catalytic step to catalyze different reactions in different pathways and includes such proteins as N-acetylneuraminate lyase, MosA protein, 5-keto-4-deoxy-glucarate dehydratase, trans-o-hydroxybenzylidenepyruvate hydratase-aldolase, trans-2'-carboxybenzalpyruvate hydratase-aldolase, and 2-keto-3-deoxy- gluconate aldolase. The family is also referred to as the N-acetylneuraminate lyase (NAL) family.	5.98831e-93
NZ_CP036292.1\|WP_145123662.1\|6806906_6810053_+\|DUF3386-family-protein	gnl\|CDD\|371771	pfam11866, DUF3386, Protein of unknown function (DUF3386). This family of proteins are functionally uncharacterized. This protein is found in bacteria and eukaryotes. Proteins in this family are about 220 amino acids in length.	1.2293e-33
NZ_CP036292.1\|WP_145123655.1\|6790445_6791792_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|99747	cd06454, KBL_like, KBL_like; this family belongs to the pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). The major groups in this CD corresponds to serine palmitoyltransferase (SPT), 5-aminolevulinate synthase (ALAS), 8-amino-7-oxononanoate synthase (AONS), and 2-amino-3-ketobutyrate CoA ligase (KBL). SPT is responsible for the condensation of L-serine with palmitoyl-CoA to produce 3-ketodihydrospingosine, the reaction of the first step in sphingolipid biosynthesis. ALAS is involved in heme biosynthesis; it catalyzes the synthesis of 5-aminolevulinic acid from glycine and succinyl-coenzyme A. AONS catalyses the decarboxylative condensation of l-alanine and pimeloyl-CoA in the first committed step of biotin biosynthesis. KBL catalyzes the second reaction step of the metabolic degradation pathway for threonine converting 2-amino-3-ketobutyrate, to glycine and acetyl-CoA. The members of this CD are widely found in all three forms of life.	5.9703e-136
NZ_CP036292.1\|WP_145123656.1\|6791876_6798368_-\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|225858	COG3321, COG3321, Polyketide synthase modules and related proteins [Secondary metabolites biosynthesis, transport, and catabolism].	0
NZ_CP036292.1\|WP_145123663.1\|6810205_6811696_+\|DUF2271-domain-containing-protein	gnl\|CDD\|224394	COG1477, ApbE, Membrane-associated lipoprotein involved in thiamine biosynthesis [Coenzyme metabolism].	1.12567e-48
NZ_CP036292.1\|WP_145123658.1\|6801568_6803089_-\|HlyD-family-efflux-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].	7.62208e-28

>NZ_CP036292.1|WP_145123664.1|6811777_6812386_+|peptidase
MPPDPKPSRWLYRKSAAAFRWLHIYLSMLSFASLMFFALTGITLNHPTWLGGSVQNVIDQSGQLPTQLLAGEVDELEIAETLRAEHRLKGRVKEFETDDYECMLVFKSPGYAADVFIDRETGNYSLTVTSSNAVAIMNDLHKGRDSGPAWSLLIDGSAILMAIMSLSGFGLLFYLKKRRAAGVLTALAGTIAVLAVWILGVA
>NZ_CP036292.1|WP_145123663.1|6810205_6811696_+|DUF2271-domain-containing-protein
MFRIPLTLIAAIFLSASLSADEHRFQHENVLGTLLTLDVHVASPQLARTIESESLTEIGRLDAIFSSYRDDSELSRWLKQPVGVDAALSVELIAVLQRAERIRRESHGAFDIRAAAIAELWKSEANAVRSPSDALRNQMVQSLAEPAVSFSNERVRRLTDHRINLDSLAKGYILDRVCEVVSKHLSPGDRFSINVGGDLRTIGAGATKIVITDPRRPSENAKPLVEFTAHGEVAVATSGTYRRSLQISERKVPHLFDPRSALPVGHAISASVIAADAITADALATTISVFPTHEALQWIDGKPGCECLIVDGEGKVHRSANWPTADPSPASRLIAAADAKQAGIHVWFKLERPSGSSYRRPYLAVWLEDSDGFPVKTAVLWLQTEQPGPRWHRDLTRWYRNDRMRKIIEKTDLIEAISGATRGPGEYEAHFDGTDNSGEPLPTGRYTLCLEAARENGTYKIIRQRIDWGTDTVEKTQLKGNIEIPQAAYQIVPAVQ
>NZ_CP036292.1|WP_145123662.1|6806906_6810053_+|DUF3386-family-protein
MPFRPGICPNQTIIKSNMMNRIYFLHLIAATTLVAASVGRAEESQTATAKPAVTATDKTARDAMQAAHDARLAWIDFPGFTADVRVQTDGVAHSGSILVTDDFDYELSISDDAIQPWVNSKLRSVIGHRRPGSAATEVKLAESGASADFGLFVARLDGSGTFRIQDGLIREVHRKNDSRWFEITNVEFFDAGEGKVLPETSSVTYRDPKTGDITKNVVNRFTWTSVGDFLLPEGCLTIETSADGGRQTRQLQFTNHKLSQNAPPQKTKLLSSSKLHRPLPESLTSFGAAVVGEYLYVFSGHSGDAHGFGKDLLVEHFRRIKFDDPAAQWEELAMHQSAQSTALVTDGKYIYRVGGLSFLTGETESEAIFNSTDHFARYDIEADKWTDLAKLPEPRSSLDAAVVDRKVYAVGGWNLQGKDGSRDAPWNETVSVFDLDQPDAGWKTIDGPGYKLRAASVAEHDGKLYVLGGISPGGFLRKTSVYDPSTSTWSEGPEMVGDSPMTGFATSTFAVGGHLYSTGASGVVYRLKSDGQAWENADRLLYPRMFLRLLPVGEDRLIALGGTGASGAGRLSVVESLRVDPNKQPGEKLVSWTVPYAGKAKHSQALVLDGTTLYAMGGNASRKPHDFSREAFVAEAFAFDIANQSVTALPEMPFAVQSGAGVVNRQTSEHKTIVVAGGMNFGEKEFHSIDSVLQFDPEAKKWSVAETKLPVPRAMADAVAHDDALWLFGGSDAGGDQGLARSVLHWWGDQSAIAALPEVELPHPRRSFGGAKIGNEYFLIGGLGDGTGIESTVDVFDMQQRTWRTAPSPSTSRVFPSVCVDGKKIYLFGGFSNDEGHFAPCSKLEVYDSETDSWSTLAESLEGVDASMNLFNMSGRLLFFGIDRNNDELAQFHLYDPNPAAVPEKFAAMGFGGRRGGNEASKNAKMLMRKDVDKDGKLSREELGKRMADFAAAADTDGDQLISFTEAKAKMEADAAAEKEAAAESAPKTEKKNDKEPKRAKGKKSKAATGSGEAAQAKADALQRDADAAQRKADQAQRDADKLRRSAS
>NZ_CP036292.1|WP_145123661.1|6806576_6806861_+|hypothetical-protein
MKTNWLKVLATCVVLAVLPGCGEEQPPAAPAGPPLPLSVEEWKQLPIEVKYDEATFDRLRDKDAKLQNDRNWHRFMKEVVVPERKLDIPGIPGA
>NZ_CP036292.1|WP_145123660.1|6805594_6806533_+|DUF1559-domain-containing-protein
MSSKDLRSRAGFTLVELLVVIAIIGILVGLLLPAVQSAREAARRMSCSNQLKQVTLATHNFHDTFLELPYATRDRLEGDDGSTWATGHIQILPFLESDAIASRWDPEEPRNSTVDTDGDGWTNDMLKKEIIPTYMCPSMVMPSAPLTGERAPMSYLYCAGTADASMLHYAAYYALPEPTYDGAIVPVMTYLASGSTPTPSHRNPTKFRDMLDGTSNTFLMGETDFMPKGVPSTSYGGVWAYGYAGYSWGTTYHPFNRHDWTSTVYGAFRSQHPGGGQFSLVDGSVRFLSESVDNDVYQAISTRAGGEVATLP
>NZ_CP036292.1|WP_145123659.1|6803379_6805275_+|efflux-transporter-outer-membrane-subunit
MPTLTRAACRDKLYKGRDRTDRTYATAGSLPAISRIHRPMLSNEPKRPIAAAACPLGGRIRAVGLAAWSIAWLLSLGGCGYLAQWKTNGHMVGPDHVAPTAAVAEHWIDFNNPKLISSQNGVDDENWWRMFRDPEIEQIVSAANSNYLPLRIAMLRIQEARLQRAIAVGNLLPQSQEFFAEFQRIQNSDNGNQIGIADLGNTFDLYQFGFNANWELDVWGRLRRQIESEGAKVQGTIEDRRDVKLSLVSDAIAAYIEIRTNQDRLVFAHANIEAQQKTLELAESRFKNGSVSKLDVTQARANLEATRAAIPELERSLRVANNQLCVLLGLSPRDLIAQMGWAGVPTTPDAIMVGMPVDLLRRRPDIRSAERAIAAQSAQIGVAAADLFPTFSLRGTINWQSFNFPDLFESASNAGAIIPGVRWNLLNYGRLMNNVQIQETRLERTIVEYRQTVLRAGSEVEDAMIRFVKAREQIASRERAVAATAESIEIATLQYEEGTVEFDRVNELRKDLVRQQDLLALARGEAALGIVAIYRTLGGGWGSADQAIGNCAPAPTIQAEPAPPIRSIPSQESKPPLTANRSPQVIVRTIGILTPLPSSPYQPLEAIQPSSLGAAKSRRQAESSTSPGSHR
>NZ_CP036292.1|WP_145123658.1|6801568_6803089_-|HlyD-family-efflux-transporter-periplasmic-adaptor-subunit
MNVQEAPYRAPLTTAGRRRGGGIQVALATMLLVAVAIGVGLAASSMQHSDHPAPDRSPGESSRPHTAGGSASTLPVETMQVQRVESYARERTFTGIIKPARQSELSFERQGEVVEVSADLGDRVEKGQPLARIGDRRLKVKRLGLEAQHREALAVLAELEAGPRKESIAAQRATVQDLAAQVDAADQMAKRRQRLLLASASSREEAEQAAFSLTAVEARLQSAQKVLDELTAGTRQERLDAQKAIVAQFDASIQDVDIEIEKSQIVAPYDAFVTERSVDEGSIAQPGSTIFRIIEDASLEVWVGVPTAIAASIQTGETLPVIVRKQSFDATVRSRIADLDHQTLTQTIVLTLDDVSPQQIVPGEVARLAFTQEIPVDGFWIPLAAISRGGQGLWSVLAVVGDGDETTTTERRDVDLIETQGERALVRGTLETGDWIVSSGTHRLTTKQAIRVPEPTDEVDESATAPATEPASQDVMSPAEKPPEPLDLVPTPRSDRPIASLAPTAS
>NZ_CP036292.1|WP_145123657.1|6798444_6801549_-|MMPL-family-transporter
MLSNLFYRNRRLLCLAVGLIFVAGLSSYSVLPRAEDPELTPRFAIVNTVVPGFNATRVEALVTERVEQAIREIDEVKEITSSSRAGVSTIGIELNANVYAVDEVWSRVRDKIDAVAHELPAGTLDPVFEKVKIKANAMLVGITWQRGGDPNYSLLRRLAKQLKEQLERIAGTESVDLYGAPDEEFLVTVKPEELAALKLTASDIADQLARSDAKVSAGQLRGASSDLLMGIDNELDSERRIAGMPIRTSDDGPVVQLGDVAEIQRDVVRPLTNVAVIDRLDAVVLGIRVRSEYQIGPWNRDVTGRLAEFESSLPPGIGIDKLFDQNDYVDKRLAGLGQNLLLGCLAVFLITFLMMGLRNALVVSFSLPLSSMMVLAGMRLLEIPIHQISITGLIISLGLLIDNAIVVVDETSHRIRAGSAPADAVAAAVKHLLVPLFGSTLTTALSFAPIAIMRGPDGEFVGAIGVSVILAIASSFLLAVTIIPALAAMGRVRPDRSHWFAWFDRGLTIKPLAAAYRSLLQMSLAVPALGIALGLVAPILGFLMVGSLPIQFFPPADRDQVYIDLELNAHASIHNTRDTARRLTETLTAHPAVDAVHWFLGESAPTFYYNVVRSRRNLPSYGQAIVKLRTDVATPEIIHDLQALVDNRCPFARVLVRQLEQGAGFDAPVEVRVLGPDLDQLRRLGTEFRDLLVSTPGVIHSRVQLDEAVPKVAFSIDEAEARIAGLSHEAIANQLQTTLEGSTGGAVVETTEQLPVRVRAGNKRRSSMSEIASINLLASQPGRSGSSIPISAIATIGLEADSAEIPRLDGQRMNEIQGFIPAGMLPSTVIDDFKRRIATANIPLPVGYSISFGGEEKTRNTAVDNLMASVVVIVVMMVAAMVLTFGSFRLAALIFVVAGLSFGISHLAVWISGYPFGFMAIVGTMGLVGVAINDSIVVLAAIRREPTARTGDLDALVDVVMRSTRHVTATTLTTIAGFTPLFLAGGGFWPPLAITIAGGVGGATLIALFFVPAVYVLIAAAQEQPEISPSIEAT
>NZ_CP036292.1|WP_145123656.1|6791876_6798368_-|SDR-family-NAD(P)-dependent-oxidoreductase
MTDQPLAVVGMACRFPKGLDSITQLWEALKTRFNAIDTIPADRWDVDRYYSSNPVSKGKAYIRRGGFLHQDPTTFDASFFGISPREAENMDPQQRLMLEIVWEAFENAGIPLPDQAGKSIGVYVGGFMLDHMITQISSRNRSQINQHSAAGMMMTMLSNRISHTYDLRGPSLSIDTACSSSLVAFHYACQDLWRGTAQMAIVGGVNVMMRPEYPMGMCKGHFLSRDGESKSFDARGDGYGRGEGAGVVLLKPLEHALRDGDEILSTVIGSGTNQDGCTAGISMPSGAAQRALIQSVCQRYQIHPLQIKYVECHGTGTAIGDPTECQAIGEIYGQGRHGEDRVVIGSIKSNTGHMEACAGIAGVIKGVLTTLYRQAAPLANLQTPNEAIEFEKLGLRLADDLIPLGRGDEPICVAVNSFGYGGSNAHVILQSAPAHHAQPNFAKHHCNGKSHANGHPQGNGSAHCNGNGNGKPLDGGALLSGNASLNPHELPLMLPVSARSTEALRANAGNLESCLANEGELHDVLYTAARRRAHLAQRAVVIGSDRNELRQGLRSLAEGQDSPHVVVDSQPFQGRRECVFVFTGMGPQWWGMGQQLYRKSDFYRQAVEQADMLFQEIAGFSILTEMLKGESSSRISRTQYAQPANLLIQIGLLEMLEDAGVTPAACVGHSVGELGSAYAAGVLSLEDVLTVSFHRSQLQATTAGTGSMLAVGLGKQEALQRIAGIGDLVSLAAVNGTNTVTLAGDTDTLTELSRQFTAADIFNKMLTVEVPYHSPLMDPLMAALERRLSGLQTSAAKIPLYSTVTGRLVTEASFDASYWPLNIRQPVEFADAVDSILDDGYNTFFEVGPHPVLSSALRDCIHAAGKECRLVHTLHRKQPEIQSVHRAIAGVFAAGCEYEWSRLYRTGKLVSLPNYAWQRERLWLENDRAAQDRINPIIHPILGTQEALSAPVWRNDFDHEAVAYLRDHIVAGIPVLPAAAYIESLLELAAIQFPDAAKLAIRDLQIAAPMIIAPDRGLDFTTTYDASRQSAQIRSLENGRLGTGQVHVTASIAPLPASETKALDLPDLLAKLDKPADVDSFYRELRQVGLMYGPYFQAVKELRIDRTDRRVLARIEIDDTLREHPAKYKMHPTLLDGCFQTLMSLLVHSETTYLPTQIGELCLYVDSLPDTIWCLGKMTSQTDRQITCDLTLCDDQGQVVGVVRSLVATAANRPQRTDQFGDVVKRQILDYQWRIADTLDEPRRLGHWLVVGASNDVAQQVSMQIENYGAMISGRVEFGDAFVDDGGLFCIRPDSVDDARQVLNRCGELDGVVFFNSLDVMVAQQDPTGEQSIAALVTLTQAMLEIEPAGRPRAYVVTQSAFAVDEEDGRVEPRQTAVNGFVRVAANELEGFQFTSVDLPASTDHATCDAVALELLCDAVEDEVAIRNLARWTSELLESPCLDDDRIEYRIPGDQHPIQIRPLRPDTEQVGTVRILAAPQPAIGPRDVRVRVEKSLLPLNLVLDQSADHIEQPLIEIVGTILEAGSEVDDLCAGMQVCGFAPADLASQLSGRRDHFHLVEIPSTDHAPQLVANLGILVQAQCALHGIDLESGDAALVDTSPMSLAVAELLAARGVRVSVVTQDAAVAEQNLPSNYNIVPACPESLHNAVQQETGGRGFAVLVAGMQSWLTSFDLRVIAAGGAVIDTDDIPQAFSLPTTIASIARTDLAVLAAKPGRLRAALEHVVGELLEIESPECSALEVSVADVAWQVLPLRETKTQVVISYDTRGQDLPIVQRDDLRLRTDATYLITGGFGGFGRKTARWLIEQGARHLVLTGRAGADDDDKKAFVQELESLGATVQDAACDTSDFGQVQSLLGTIQNQMPPLKGVFHSAAVIMDQAIADINLPALQSVLRSKALGAWNLHRATEDLDLDHFVLYSSLANQVGNSRQAAYCAANGFLNGLAHHRKAIGLPATSVCWGAISDVGVVARDEKLELFLRYVGLRGLPSAEALGLLRQGLARDVTQFGMVLITSWADWARFETLGGKSPRFAALIEADSAPQDNALRDQLIEELAGLSDADQIDLVAGLIREIVGVVLKSDPEAIAVDRPVSELGVDSLMATEIQQMFDSQLGLKVSVLELVGEATIRSLAVGSLASLGTATSLPSKSDSRPAASPDPTAAAPV
>NZ_CP036292.1|WP_145123655.1|6790445_6791792_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MSVKSSLERLKMQIRREGSDSEENNATKKTSKPRGEVKASPAFYQFDKFPEYKEFTTMEWYLDKEKYPRTQFLKRLSVSDATVNLEGREMINYSTYNYLGLAGDARVKEAAKRAVDTFGTSTGSGRSITGEIDLHRAFEKEICEVLGTEDAVLSVGGYSTNTFAIGYLCRNKDLIVYDELIHNSALAGCKMTAARRIGFPHNDYEALEALLAANRGKFERVLILVEGVYSMDGDIPDLPRLIDIKRRYKALLMVDEAHSFGIIGPNGLGVTDYFDFDPHDVDIYFGSLSKSFGTCGGYIAGPNPLIAMLKYFAPGVLLYGAAPTPANTAAGLESLRIMRAEPERARRLVDNARHFIQRAKAAGLDTYNSHDSAVVPLMCRDSELALWLSMALFGQGICAYPMLHPIVPRDKSRLRFFINTFHTHEQLDYTIQCIVDNLRVAPKSKGVF
>NZ_CP036292.1|WP_145123665.1|6812865_6813855_-|dihydrodipicolinate-synthase-family-protein
MAQSNRITGILTPNIVPLDPRGNVDEQTLRGYVDWLIAHGVDGLYPNGSTGEFVRFTAAERREIARIVIDQAAGRVPVLVGAAEANVRETIEACDAYGEMGAQAVAIVAPYYFKLSDEGVYSYFREIADAVSVNVTLYNIPLFASEIDLATVRRLAEECPRVVGIKDSSGDLPHMMRMIAAIRPQRPEFSFLTGWDASLSAMLLMGADGGTNATSGVVPELTAAVYKACKAGDLSEAVRLQNELTPLFDTMIGTGEFPEGFRAGLRTRGWDMGRSRQPMTAAQYDKSAQTEAKVRGMMTSYTNGAVTSASATPESIDAIVRRVLSELKA
>NZ_CP036292.1|WP_145123666.1|6814031_6816227_+|hypothetical-protein
MTSRRRKPKTQGDPHPLPPPAVEPAEPSWLRLVYQIAIPALLGVWLCVWVTQILYDGGQTDRSHPRWHLLFSLFFLPDEIFAAWTDGVVSWRGPVDRLRVLMIVTAVTLPSWLLGGQLLRVSGIARRMRGIEVAILGLAIGLSLQATATLMLGLAGWVSHRAAMPLLGGIQIAIALALGAHRSIGRDQICDTCKQLARPAGEHPLAVGLTLIGIALVAIRCLLPSNEFDVLEYHQGAPKQWFQEGRIGFSEQNIYANMPMAAEMQTLSAMSWAGALGIEDAWWWGGLAGKSTMFLYWILAIGAIGCLARRWVGGQAACWLVAVACSGLAFAEVTVLGLIEPAVACYFAAALLALAALRHQLATQPAAMFWVGFLAGSALACKYPALLFVCLPVGLLAAWQIFRQRSTVPIDFRVLGMFVLGCAITAGPWLAKNMVLAHNPVYPLAAGLLGGYQFSEAKIAQWQAAHAVPTRSLSALADSLFSIAWSWKSQGAILIPLALIGLLRIKRSPAVRIAVAIAIFVFAVWWLLTHHLERFLLPAIPLAMLLAGFGIRTMFQQLGRPLASICLTVGILCNLVLMAVSPTMGDPRLLVDTSAIRREGIEPTDSIRVPEHVLWANRNLQSTDGVLLLVGDAAIFNYEVPLRYSTCFNVSDLSEIACLPDEQWRGEFEQRGIRHVLVHWGEIDRYRGEGNYGFDPSITPELIRAMVDQGVLKPLDTGLDPQRVEVLAVGP
>NZ_CP036292.1|WP_145123667.1|6816264_6816501_+|DUF4160-domain-containing-protein
MPTVLRSGPYRFYFYSHEPNEPSHVHVDRDEDSAKYWLQPVSLARNLGFRGHELREIERIIGDNQQELLEAWNGRFGN
>NZ_CP036292.1|WP_145123668.1|6816481_6816766_+|DUF2442-domain-containing-protein
MAGSEIKPGERVKDVHFGDDAFSVDLLDGRTITVPYAWYPRLLHASPEHRANWRPCGGGFGIHWPDLDEDLSTEGLLRGAPAPREAEQAGGRSN
>NZ_CP036292.1|WP_145123669.1|6816983_6817979_+|hypothetical-protein
MRSPSQIFDFTPSGLRLGRWRGTTYAIGWSYLGLGAVLFVAAWWLKVWPGNQDLPWLALVVWLAIGFVGGLQESAHAVTAWLLGGKSRLMMIAGHGGAGQYRIFGGPRQAIVAAAGPASSCLLALLVAGILMFRGEASLWQMLDPLRPPELVGRLNLVSIGKVVAWIAITLSVVQMLPLWRCDGRTLLDGLVATFRPHYTPSARAHAAAVVIGWIAFAMVGLSLGVAMFEDRQGVPRWPVLAAVGLVLWMSGQKVDPRIRVIDAKHQPIGWLGARRIRQAHHREIREASDIAQLDAILDRMTQHGADSLSHADRAVLKRASLALKRHSNKS
>NZ_CP036292.1|WP_145124322.1|6819009_6819810_+|hypothetical-protein
MTAGGGAIGILIVLYALLQPILSKQLGIDLPKFPVKVGADAPMVAGPDKPTEPSTEDSKSAAPKIVVQSPSGDRPVDKDSAATNTASKRDRQDSATPKTGSGPLSQFNRSSKSDDAKLSPTKSAPDKTSSAKSDPSLKYGILKSIGRDSYMSPAGLRYTPGSQEGHRLKHLERHTADQPSRPGKHGVFDGGMEKTLLVLDQAYEKGTKGGHGTTKTQDDGRTIYTVDMGKRVGYIGGRDGNRMRKPMARRVRIVLDGDRVITAYPL
>NZ_CP036292.1|WP_145123670.1|6819972_6820287_+|hypothetical-protein
MTPHYSIDYCPRCGAGLLGIRICGLGTDEPHGLVVCDECESIWLEPDVTTPHQYPDASDARCPKCSDPLWGPQSRWATREDLVQLGWQDRVDPELNGEPDDHIA
>NZ_CP036292.1|WP_145117411.1|6820482_6821907_+|IS4-family-transposase
MQPTSIAYEFQDIQLGDKRLNDRAEALLASLAANPSASINEACSGWDETKAAYRLFDNPNVDPEAILGAHAEKTLQRIKAQDTVCIAQDTTELDYTAHPPEGVRNLDRLGRRGLYDHSHIAFTPEKLCLGVVGVKFYDRDKETLGTSKKREGQPLHTGEGQRWLDGYRKACEIAGKCPETQIVSLADREGDIYDIFVEADQHETPAQFVIRSQRKRSLPEKDPDGGPAAYRKMRAEIASAQPVAYREVQLPQTPKRTKGSGNKQHPGREARTAKLEIRAKRMTLRAPHNKQSSMPPVEISVVWVSEIDGPGDGTEVDWLLLSSLPVDTIAQTLRIVDLYVARWPIEVFFRVFKTGCRVEEIQLEARDRLIRALMFYKVIAWRIMFVTFLGRECPELPCDVVFSEAEWKSVWKVVEKTAPPKQAPELSQFIPVLATLGGYNHREGDGPPGAEVIWRGTRRMLDFALCWQAFGPDQ
>NZ_CP036292.1|WP_145123671.1|6822001_6822613_-|thymidine-kinase
MAKLYFYYSAMNAGKSTILLQSSYNYRERGMNTLILTPELDTRFGTGKVSSRIGLEADAIVFDQVENLRHCVQTQVEAAPLHCVFVDEAQFLTAKQVRQLSDVADQLGVPVMCYGLRTDFQGNLFDGSMQLLAWADVLTEVKTICHCGRKATMVLRIDQHGSPIQQGDQVQIGGNERYLSVCRRHFKQGMASRQTDELPFDET
>NZ_CP036292.1|WP_145123672.1|6822745_6823660_+|DUF1571-domain-containing-protein
MNRNQILLLIVIGQGLVIALLFAIRFKRESADPEDSIAVVEVAEQMQQAPSNARESTLAEALTIARAGLAEMRANMTDYRGRVVKRERIKGQLANEYEMEIKVQCRRLVEEEVVAPMRVYLKFLQPQSVAGREVIWAEDQNDGRLIAHEPGLLNVAQASLDPHGERAMEGNLYPITEIGLVNLVVQLIARGENDLEESQVRVTLAEGQTIGDRECQQIRIELIQPHDELNFQYAEIFIDSERQIPLRYAAYGWPEDAATGDHDGPPELLEEYTYYDIQTNVGLTDADFDPNNEAYDFPAFRINL

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Crispr_ID: NZ_CP036292_30

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_30

7198253-7198354

Orphan

Consensus_repeat	Method
CGAAGATTTGATTGTTCGCTGAGTTCGCCAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_30

>merge|NZ_CP036292|30|7198253-7198354|CRISPRCasFinder
CGAAGATTTGATTGTTCGCTGAGTTCGCCACGTTTCATTACGTCAACTGTCAGCGACTTGCCGGCAGCAGCCGAAGATTTGATTGTTCGCTGAGTTCGCCAC

>NZ_CP036292|30|29|7198253-7198354|CRISPRCasFinder
CGAAGATTTGATTGTTCGCTGAGTTCGCCAC	GTTTCATTACGTCAACTGTCAGCGACTTGCCGGCAGCAGC
CGAAGATTTGATTGTTCGCTGAGTTCGCCAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123896.1\|7205770_7206217_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123894.1\|7201509_7204614_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123891.1\|7198400_7199396_+\|general-secretion-pathway-protein-GspF	unknown	unknown	gnl\|CDD\|224376
NZ_CP036292.1\|WP_145123887.1\|7189580_7190369_-\|YchF/TatD-family-DNA-exonuclease	unknown	unknown	gnl\|CDD\|238635
NZ_CP036292.1\|WP_145123899.1\|7208352_7212195_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|215358
NZ_CP036292.1\|WP_145123890.1\|7196294_7198130_+\|SLC13-family-permease	unknown	unknown	gnl\|CDD\|238535
NZ_CP036292.1\|WP_145123900.1\|7212271_7213378_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|223506
NZ_CP036292.1\|WP_145123892.1\|7199411_7199951_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123895.1\|7204610_7205771_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP036292.1\|WP_145123886.1\|7188784_7189462_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP036292.1\|WP_145123884.1\|7185881_7186790_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP036292.1\|WP_145102378.1\|7192780_7194184_-\|Si-specific-NAD(P)(+)-transhydrogenase	unknown	unknown	gnl\|CDD\|235373
NZ_CP036292.1\|WP_145123893.1\|7200000_7201263_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145102379.1\|7194354_7194573_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123888.1\|7191404_7192463_-\|phosphoribosylformylglycinamidine-cyclo-ligase	unknown	unknown	gnl\|CDD\|235439
NZ_CP036292.1\|WP_145123885.1\|7187341_7188736_-\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|223650
NZ_CP036292.1\|WP_145123898.1\|7206571_7208218_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145123897.1\|7206261_7206579_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123889.1\|7194569_7196150_+\|sodium:solute-symporter-family-protein	unknown	unknown	gnl\|CDD\|271357
NZ_CP036292.1\|WP_145124347.1\|7190376_7191345_-\|phosphatidate-cytidylyltransferase	unknown	unknown	gnl\|CDD\|226955

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145102378.1\|7192780_7194184_-\|Si-specific-NAD(P)(+)-transhydrogenase	gnl\|CDD\|235373	PRK05249, PRK05249, Si-specific NAD(P)(+) transhydrogenase.	0
NZ_CP036292.1\|WP_145123887.1\|7189580_7190369_-\|YchF/TatD-family-DNA-exonuclease	gnl\|CDD\|238635	cd01310, TatD_DNAse, TatD like proteins; E.coli TatD is a cytoplasmic protein, shown to have magnesium dependent DNase activity.	2.93049e-112
NZ_CP036292.1\|WP_145123899.1\|7208352_7212195_+\|hypothetical-protein	gnl\|CDD\|215358	PLN02666, PLN02666, 5-oxoprolinase.	0
NZ_CP036292.1\|WP_145123890.1\|7196294_7198130_+\|SLC13-family-permease	gnl\|CDD\|238535	cd01115, SLC13_permease, Permease SLC13 (solute carrier 13). The sodium/dicarboxylate cotransporter NaDC-1 has been shown to translocate Krebs cycle intermediates such as succinate, citrate, and alpha-ketoglutarate across plasma membranes rabbit, human, and rat kidney. It is related to renal and intestinal Na+/sulfate cotransporters and a few putative bacterial permeases. The SLC13-type proteins belong to the ArsB/NhaD superfamily of permeases that translocate sodium and various anions across biological membranes in all three kingdoms of life. A typical ArsB/NhaD permease is composed of 8-13 transmembrane helices.	2.50227e-39
NZ_CP036292.1\|WP_145123900.1\|7212271_7213378_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|223506	COG0429, COG0429, Predicted hydrolase of the alpha/beta-hydrolase fold [General function prediction only].	6.83698e-59
NZ_CP036292.1\|WP_145123884.1\|7185881_7186790_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	5.82811e-51
NZ_CP036292.1\|WP_145123886.1\|7188784_7189462_-\|ATP-binding-cassette-domain-containing-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.	9.87689e-91
NZ_CP036292.1\|WP_145123895.1\|7204610_7205771_+\|hypothetical-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.	0.00849869
NZ_CP036292.1\|WP_145123888.1\|7191404_7192463_-\|phosphoribosylformylglycinamidine-cyclo-ligase	gnl\|CDD\|235439	PRK05385, PRK05385, phosphoribosylaminoimidazole synthetase; Provisional.	1.80937e-178
NZ_CP036292.1\|WP_145123885.1\|7187341_7188736_-\|FtsX-like-permease-family-protein	gnl\|CDD\|223650	COG0577, SalY, ABC-type antimicrobial peptide transport system, permease component [Defense mechanisms].	9.63486e-19
NZ_CP036292.1\|WP_145123898.1\|7206571_7208218_-\|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.	4.22003e-54
NZ_CP036292.1\|WP_145123891.1\|7198400_7199396_+\|general-secretion-pathway-protein-GspF	gnl\|CDD\|224376	COG1459, PulF, Type II secretory pathway, component PulF [Cell motility and secretion / Intracellular trafficking and secretion].	1.06651e-38
NZ_CP036292.1\|WP_145123889.1\|7194569_7196150_+\|sodium:solute-symporter-family-protein	gnl\|CDD\|271357	cd10322, SLC5sbd, Solute carrier 5 family, sodium/glucose transporters and related proteins; solute-binding domain. This family represents the solute-binding domain of SLC5 proteins (also called the sodium/glucose cotransporter family or solute sodium symporter family) that co-transport Na+ with sugars, amino acids, inorganic ions or vitamins. Family members include: the human glucose (SGLT1, 2, 4, 5), chiro-inositol (SGLT5), myo-inositol (SMIT), choline (CHT), iodide (NIS), multivitamin (SMVT), and monocarboxylate (SMCT) cotransporters, as well as Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. Vibrio parahaemolyticus Na(+)/galactose cotransporter (vSGLT) has 13 transmembrane helices (TMs): TM-1, an inverted topology repeat: TMs1-5 and TMs6-10, and TMs 11-12 (TMs numbered to conform to the solute carrier 6 family Aquifex aeolicus LeuT). One member of this family, human SGLT3, has been characterized as a glucose sensor and not a transporter. Members of this family are important in human physiology and disease.	2.59051e-63
NZ_CP036292.1\|WP_145124347.1\|7190376_7191345_-\|phosphatidate-cytidylyltransferase	gnl\|CDD\|226955	COG4589, COG4589, Predicted CDP-diglyceride synthetase/phosphatidate cytidylyltransferase [General function prediction only].	8.70386e-78

>NZ_CP036292.1|WP_145123890.1|7196294_7198130_+|SLC13-family-permease
MVWESWFTIAIVCVLLYALARRWASTDLLVLASLAALVTVGELSTAFALDSRSLNPEATFYLPTVAQAIDGFGSRSVVTIALLFAAVVGLELTGGTELATSWLLRRPKSAVDAQLRLVAPVAALSAFLNNTPIVAAMLPVVTDLAKKMQVSPSKFFLPLSYAAILGGMCTLMGTSTNIMVYDMIQQSPGGRPLHFFEPAWVGLPATLIGILYMTVGSRWLMRDRKPAVSTSDDPRQYTVEMEVVPSGPLAGQSIEDAGLRHLPGLYLAEIERGGEVFQAVRPTQKLQSGDILIFVGMLESVVDLQKIRGLEIASEQARKVAAPAWNRSLVEAVVSPRCPLVSKSIREGGFRTHYGAAVIAVARGDRRVPGKLGDVVLQPGDVLLLDAPASFTQSRRDTRDFFLVSAVENASVRRPERAWIALGVITLMVLAAASGFLDLTTAALCAVIAMICSRCCTSTEARRGIDWSVLVVIGAALGIGKAMETTGAAAGIADTILLLAGNNPMFVLAAVYLSTMICTELITNNAAAALMFPMAWSAASSMPGVDPLPFAIAVMIAASAGFATPFGYQTNLMVYGPGGYRFTDYLRFGGPLDLIVFAVAMVMIPWVWPLQ
>NZ_CP036292.1|WP_145123889.1|7194569_7196150_+|sodium:solute-symporter-family-protein
MIQLVVILIYLALLITLGLAANRLFRGTAKDYMFASHSIGPFLLLMSLFGTTMTAFALVGSTGQAFRAGAGVYGLLGSASGIVHSLCFFVIGVPLWRLGQRNGYRTQIQFFRDRLDSHAIGFLLFPILVFLVIGYLMVGVLGGGAVVEAVTQGAFEKSGMFAASGYGVPSAIASAVICLVVLVYVFFGGMRGTAWANAFQTAVFMVLGVVSFVVIAGAIGGTDSFIENLRIASSQVDESQLTRAKIPKPLFFSFLLIPLSVGMFPHVFQHWLTARNANAFKLPIVMHPIFIMIVWVPCVLLGIWASGPESGIADALAAMDPHDRGNAVLGLLVSTHAGPLLGGLLCAGILAAVMSSLDSQFLCLGTMFTEDVLQTGDSEGRDDQKTVRIARTFVVAVVLATYCLSLVLPRSVFDLGLWSFAGFTGLFPLVFAAIYWRRLTAAGAIASVIAAISTWFVLFYRSDFGGNPRYSFPEQPLSLGFLQVPPLHPVVAVFVVSAITLVLVSLVTKRPDAATLEKFFGGSPQK
>NZ_CP036292.1|WP_145102379.1|7194354_7194573_+|hypothetical-protein
MKYLIWFLIVVLVVLHQDYWQWNNATLDFGFLPRAISYHVGISIAAATLWLLATKFCWPDAAIEGELKEGDR
>NZ_CP036292.1|WP_145102378.1|7192780_7194184_-|Si-specific-NAD(P)(+)-transhydrogenase
MSNSTYDYDVLVIGTGPGGEGAAMQAAKAGLRVAVVERHTSIGGGCTHWGTIPSKALRYSISSVMNALGSPVLRACGVHANPTMKQLRSSAQQIIGKQVSMRQTFYDRNNVPVLVGQASFVDDHTIRIDGQSDQKVTANKIVIAVGSRPYHPPDVDFEHPRIFDSDTILGIDEKPFSITIYGAGVIGCEYASMFRNLGIKVNLINTRAKLLEFLDDEIIDALAYHMRDQGVVIRHNETLDKIEGVDDGVILHLKSGKQLKSDALLWANGRQGNTDGLGLENVGLTPDKRGQLEVDEQFQTARDHIYAVGDVIGFPSLASAAYTQGRAAARHFSDSVEVESNLRIRDIPTGIYTSPEISSVGKTERELTEECVPYEVGSSQFKSLARAQITGRTAGMLKILFHRETREVLGVHCFGAEASEIIHIGQAIMNQPEGHNTIDYFVDTTFNYPTMAEAYRVAALNGYNRLF
>NZ_CP036292.1|WP_145123888.1|7191404_7192463_-|phosphoribosylformylglycinamidine-cyclo-ligase
MPVTYKDSGVDLDLYAQAMQRLPSLARRTFSPRVVSNDGGFAGLFKLDFSSPLFSRNYEDPILVAGTDGVGTKLKVAQMTGRHDTVGIDLVAMCVNDLICTGAEPLFFLDYIAMGRDDADRLEQVVKGISDGCLQADSALLGGETAIMPDMYAAEDYDLAGFAVGVVDRKHLVDGKSIVPGDKIIGISSDGIHSNGYSLVRKIISHAGIALDACPAELGGASVADELLRPTRIYSSMLRRVLGHYRVKHVVHGIAHITGGGLHENLSRILPKTVDTVIQPDSWPMPPVFPWLQGLGDVADEEMQRVFNMGLGLVLVVSDFYAAKIMELVRAGGCECTEIGHVEAGSGESRFA
>NZ_CP036292.1|WP_145124347.1|7190376_7191345_-|phosphatidate-cytidylyltransferase
MTTSTFWLLGVVVAVLAILLLTGRLLERRQSSMMNPALLQRFNHRVRVWLMMSAILVFAFLMDQFIRGVTVLLFGFVSFWALREFVTMTPTRRGDHRTLFWVFFIFTPLQYVLIALGPAYYGLYSIMIPVYGSLFIPARNALAGDSKRFLERTAKIQVGLLICVYSLSYAPAMLDLNLSSSRKVQWDGSPVSLLFFFILIAQIADVLQQAWNRFAGVHVIAKEINASRTWEGLLGSIVSTGAIGAALWWATPFEWYEAAVMSMIVAMMSSAGTMTLSAIKRDRGVTDTGTLVQGHAGLLDRIDNVCFAAPVFYHLTRYFFSV
>NZ_CP036292.1|WP_145123887.1|7189580_7190369_-|YchF/TatD-family-DNA-exonuclease
MKLFDTHAHLDNPRYDDDRDALMQRSRDAGVVCTLAMGTTAASSRKCIEIADRYPDVYAAVGIQPTYVGKPDAGDWDEIVELAKHPRVKAIGETGLDCYWDDNAPLPLQQTLFEQHIELSRQTGLPFIVHMRNSEVEVLQVLQDAGKQGPVNGIMHSFTGDWELAQKCLDLGMDISFAGMVTFKKSQDLRDVAAKIPADRILIETDSPYLTPHPFRSKRPNEPWYVQHTAECLAEARGVSVQQFADQTTQNACRRFAIALDA
>NZ_CP036292.1|WP_145123886.1|7188784_7189462_-|ATP-binding-cassette-domain-containing-protein
MLELVDVKKQFPQPGGGTLTVLDIPKLSIDAGEQVVLIGRSGGGKSTLLHTIAGITKADGGKVIVNGYDIARLSEAGRDRFRAGAIGYVFQTFNLLGGFTALENVRLGMTFGSGRHDIARARHLLERVGLADRMHYKPSQLSVGQQQRVAIARSLAGRPKLLLADEPTANIDPANQQTIIDLIRDTCREEQVALLLVTHSMQVAEQFDRIEKFEDLNRAMATASI
>NZ_CP036292.1|WP_145123885.1|7187341_7188736_-|FtsX-like-permease-family-protein
MNLFKIAWRNAQQRGLSTLLTTISLALGVGLVVLVLSIHGIVSDAFQRNATVGYNLVVGAKGSPLQLTLNTVYYLSQPVENLPYDYYLEFFGQEERERQLAAYGGHLDEPDRPGKFSLYTGSDSGGLVIPVCLGDYFGEYRVVGTTPAFLDNLKHGPDVDQPYEFREGRNFQTHSEENGFFEAVVGSRVASTMNIKVGDTFNPTHGDPDGKGHDLGFKIVGVLKPTGTPNDRATFVNMEGFYLMEGHAKPSEHGDEEEEAEVEEEVVVAGEEGAVPNTPLPLDQREVTAILLRPSQTMFAMMLQNVINEGLQAQAATPIGEISKLMEQFVDPIRYVLLLITAITCIVAGVGILVSIYNSMNDRRRDIAVMRALGARRGTVMWIILLESGMIAVLGGLLGWIAAHGAIALASGTIEDRTGVPVNFFSTTSAELYVLPLVLGLAAIAGFVPALVAYRTDVSRALAS
>NZ_CP036292.1|WP_145123884.1|7185881_7186790_+|LysR-family-transcriptional-regulator
MELDQLRNFLRVAEFGNFTRAAEAIGLSQPALSRSIARLEEELGQPVFERQPRLIALTDAGHILHDRARQILALVDDVHREITDDGETGTIRLAGIPTIVPYFLPPLLREFGQACPAATVRVQEDTTEVLLKQLADGETDLAILARPLDAKHLDFEDLFEEELLLVMSPQHPLRDKPQIHLADLDAMPFVLLGEAHCLTRNIVQFCQQKSLQPVSVERTSQLASVQELVTLGHGISLIPAMARALDASDRRIYRSLAGNQPTRQIVMAWNPYRFQSKLVLRFQECLRSFVQNHPPKAPGHES
>NZ_CP036292.1|WP_145123891.1|7198400_7199396_+|general-secretion-pathway-protein-GspF
MSQTVSARFCRRMATGFHAGVDLLKLCQREAQHGSPKHKAAMEAVAAQLRDGTPMARAMIDVAEGKYFPPLMIQMVHIGETTGRLERTLKELADHYDHRIAMQRMFLMGIAWPMLQLIGGIAVIGLAILITQMLGSEFNAVGLNMTQYLTLVFLFFGSITAAVLALKFNAFGCHRLFALVYRIPKAGEALQTIALSRICWTLSLALDSGMDAMRSVKMALQSTQNDHFASRADTAIATIKSGGTLTESFASTGIFPEEFLHFVEVAELSGTDAESLGNLADVYDQRAKTATRVLVGVMTGVIWAAVTIMLVAIILKMAMSVFGVYDEALKM
>NZ_CP036292.1|WP_145123892.1|7199411_7199951_+|hypothetical-protein
MMSHNKVIGSTQWMLVTLVAVGMLSSLVILRAYGQEPTSPDADQKIQDSIRSALQGESSTAPAEEPLLGDVLDLIRRQGSILDGSTLDTEDDPKPEQAKSTAVSDAHYRVAEMLLKTSRMLAALPSQSDLERQQLVRQMRRQAAKCLQSGEPTPPGDVFFQPAGDQVAPLQFGDDTNEE
>NZ_CP036292.1|WP_145123893.1|7200000_7201263_-|hypothetical-protein
MDEQDFKDLYGLMRGNSDATSVMDAQGLFALKDYQQTLEKLQGIQQRYESSKIRVMRTKIEESGGRKSSEQEAKERRLQKKQTRYREVMEKLDEMQAALPTLIQRAEARKAREQSQQAAVVDQSHEDTIDGEASEELTHSGEEQSPSLEQFIREFVAAPAATNQRDLIDRCFKVRPVSDAKDVRAGELYFIDGGGQTYLALVRKSDNPERVRLKSAITGERLRTIDLPTFLKLGQRDRVVRLKPLPQNSGSSQRTQTSTSAPAPTPAPQTTAAAPPIEDDDDVVIGGNALQESAETAKILDKGAFSQLADAANRSGICPGADLIAHVRDRDFRMGNFQDALQTMEGIYGKFTAAAASRTAQLRQEDAAIQSGRVKMSPKDLAAKRARDAAQNQLVERARNRFSRVLDGLRVLLRKETGEG
>NZ_CP036292.1|WP_145123894.1|7201509_7204614_+|hypothetical-protein
MQRFCLQIIACWLIGMVIPAAADEPARAFLDGLRARGYHDIALEYLQSLKSNPAAPADLKEAIEFERGVTLIEASRSQNDPKLRTQFLSDAEAALKAFAEANPSSPQVNAARSQLAGLIAERARMTVQKANDGGGPKLLQQATKQYNEAAAVLTELNKSVTAQLDKIPKVLDAKDRKQAELIQQRTQLRADNLQTQLLAAAIREELADTVAAGSPEQKKYLSEAASLYDGIYKEYRTRLAGLYARMYQGRCNQRLGQLRDALGYYGELLDQPDEPEAFRVLKTKTLRLAMECWLDNSQRKYREAIKQGSRWNSLARPHEDREPDWLAIRLSLAQAYKMQADDAGENDSRLVSRSIAEARELAESVAKVRSEFQDEARRLAARLGGPEDAQVEFVPENFEDAKIAGQEALQAIASSDAAVQQATRELAAAKDDAAKKSLQEKLKASQAAAQAARDKAMRLFRRALALADRDTPQSEVNFVRYFMCYLYYLEQKPFEAALMGEFVARRHPTSAGAVPSAKIALASYVNLYDLADAEDADFEADRITNLAMYIADTWPKRPEAAEALTTVIPFVINDGDLPLAKQLTQRIPAGSAGRLQAERQTGQAMWGRYITHSQQVRTWEQEGAPEGTDLAKERTQLEELQKGTIELLSAAFASLDKQGTADTTTVTAMLSLAQAYVETLQGEKAVEVLENSKFGPLALVDKKDAAVANPVLAEETYRTALRAYIGSLGSGGDAMMEKAKGVMASMQEAVADDEAGKQRMLSVYISLAQDIERQMKAAQSPEDKRALSVVFEAFLEQLSSGSNDLNVLNWVAETFSSLGAGFTTDGEIGPDAKKYYDQSLAAFENMLQRPELPEGTATQIKLRMAQVQATTGDFDAALAIFEEVLAKNAMMLNVQVEAAKLLQDWGKQDADKYLDAMNGPGSAAASVWGWAKIAKTTITYPQFRNTFYEARYEYARSALALAASQQGTEKDKLLAKAERSLSQTQKLYPTLGGDQWPAKYDETLKEVQTAMGKPAVGLPKIEQPANEADSGEGK
>NZ_CP036292.1|WP_145123895.1|7204610_7205771_+|hypothetical-protein
MSFDNLDLNGTSLMARLHGSPLPTAEEMGSPQQRRSTGRSIGLCAPIKCLAFAMLMGLPGIATAQFDQVYPLRGAPMNGEFVGSTPTEVTIKVQGTDREIAVNEIRRLGFKEDPAELKQARSRVASGDYQAAMDELKKINPASVTRPIILLDLQFYLALCEGKLALSSGGDKGSAASAMLAFVRKASKSHHFFAAAEMLGDLAVALGKYPEAIKYYGAISAQAPWPEYKMHAVMLEARALMAQKDFANAEKKFASLANATASTAETKRQQLLAQVGVARCQAETQSPEAAIAAIQKLVADNDESDAELFGRAYNALGACYLKANKPKEALMAYLHVDVLFYAQPEIHAEALYQLSKLWEQVKKTDRANAARNLLNDRYAGSRWASM
>NZ_CP036292.1|WP_145123896.1|7205770_7206217_+|hypothetical-protein
MRFRLRSLLLAVLLVAALCLGLRNAYQTIRRVTSFNASQFVASMCIEHMKANGDSWPCDWEELRDDYATCLVRSGRDWDFDDLQHRVEINFAADPHHPPSTSPASPQPDFRFLRSRYGQPSHGPNQSPDASIQTYLQSASSQKGEGAE
>NZ_CP036292.1|WP_145123897.1|7206261_7206579_-|hypothetical-protein
MSDPSKSTPIEAEIVSATLVDDAPQPEPDAKHWIEELTDNRAIVLGTLFFVTGVLGLPLLWISRQFTPLQKWLLSIVVTIYTLVLIVIVAVVLMWSWNQIQQSIA
>NZ_CP036292.1|WP_145123898.1|7206571_7208218_-|protein-kinase
MSRSRLGPLALESKLGAHPSQSSVWSAVHVEQRIRLAIKVFSLPLGGTTESRKELAAEWARLKQLQHPAIARCYGGGFEETDAYLAYELVEGETLAQQIERRGRLPWETVLDYADALIAAMVLAHDQQIIHGALEPDKIMIEPLGQPQILDFRIDRYDSPYHTNQPASLLHYACRAPELITSTSNLSVKSDLYSLGAILYFALTGRPPISGDTPEAVAAASATEVPSPINAVVMECPIWFAAVIDQLLDKDPAGRPFGTQAAQLAFVEVRRKSASGVGVAEHASAGFSPLNMKVDKQEAKKVLGRADDGVLKPVDGASFYEKAWFLLFTLVVLVGVAAWFFIPPSEDKLRASAERMLATENRTNLRIAKDEYLMPMTRRFPDGKHIDWAMEQIDQIDMLEAEYQLGIKLKHGRPIRNEAERLYSQGREYEQFGDMVSALDQYKNMVTLLDPDDEKSRPYINLAHRQIRTIEREGTQSGVRVKLIEARLSEAEALEAQGRQIEARKIWYSIVELYADNQEMQRQVQIAQDKLREVTEKSKPRESDSSDE
>NZ_CP036292.1|WP_145123899.1|7208352_7212195_+|hypothetical-protein
MIKVWADIGGTFTDCFVSIPGQPLRWTKVLSSGSIKGRIDADSTAATVIDRLRVDDPDRFWNGSVLRLLDPHGTLVEQRHVESFTAATGQLQLAEPFSQPPQPGWAYELTSDLTAPVIATRLLLRLPADQPLPPLDVRMGTTRGTNALLTRRGAPTAFLTTAGFEDLLEIGQQDRPDLFTLNIVKRKPLYSAVAAVEERIAADGTILQPLDLEAARLQIDALRRSGAESLAIGLLNAYINPAHEQALVDLALAAGFANVSASHRIAPVIKLVDRAETTVLDAYLNPVIADYVARVWQQFGGVDRCQLQLMTSGGTLVPGDAFRGKDSILSGPAGGVVALAEIARAHGAAEAIGFDMGGTSTDVSRFAGQPVRQYEAFKAGTRILTPMMAIETVAAGGGSICRFDGQRMCVGPESAGADPGPACYGRGGPLTVTDLNVVLGRVLADRFPFPMDRDAAIARLAEIQQTMEAAGHPIESAEALAAGFRAIANHHMAEAVRAVTTAEGRDPRGMTLVGFGGAAGQHLCDVAEVLGIRKIIDHPQASLLSALGMGLAATGNTQSHGIYRPLEKVSDEELTDRIEAVTQQALAELPTAPDGVAATIRETIDVRYLGTDAALEIDCRSRDEIAAAFHRQHREQFGYQRIDQPLELVAVRATVSLPGAASLQRLAEVESQACQPAAFQDVWLGDRWQQVASFDRDQLVPGAQIVGPAIVASDHHTLVVDRNWKAQVAEDLSIVLVQEEAASDRRVAVETDEATCDPVLLEIFASRFQQIANQMGLVLGRTAISVNVKERRDYSCAIFRGDGSLVANAPHVPVHLGAMGHTVRSIMAQFPEMFPGDCFVTNDPFAGGSHLPDVTVITPVFVDSDPESASDRGTRRPDFFVASRAHHAEIGGITPGSMPPDASNLNQEGVLIRGLALVRNGQQHQEDLKRLLSAGEYPSRCVAENLADIAAQQAAGTGGARDLCSLVAQYGGAVVDRYMMHLQDVAAAAVSARLRRLPAGAMQFEDSLDDGTPICVQMQVIDDRLRIDFAGTAGVHPRGFNATPAIVTAAVLYVLRTLIDQPLPLNEGVLRCVDLHLPVGLLNPTRDDDPRKCPAVVAGNVETSQRVVDVLLGALGVAAASQGTMNNFVIGDATFGYYETICGGSGATATGNGASAVHTHMTNTRITDPEVLELRYPMRLIRFAIRRGSGGVGEHDGGDGAIREVEFLKPLTVSLLTGRRTDRPPYGLAGGADGALGENWHTAADGEKQRLAACCRIEVQAGDRITLLTPGGGGYGLKPN
>NZ_CP036292.1|WP_145123900.1|7212271_7213378_-|alpha/beta-fold-hydrolase
MKNRHQHARRLRRARQSSPRDGWICLLPLLQTKELAAVSLSFQPHPLLLGGHLQTLATTLIPTPQIPYKATQHRVVLDDGDQIVLHDDTPPGWTPGQPVVILLHGLCGCHGASYMIRMADKLNRCGVRVFRMDMRGCGAGRDLARELPHSGRSGDLLAAITRIAELCDDSPIWPIGISMGGNILLKMLGEIGKGILVPEFPADRITRAAAVAPPIDPARCCRNMSRWMMRPYGLYFIRKLRSRVAPLVEQREDWRAINWNPHPRTLWDFDGLVTAPLSGFRDVEDYYAQAAAAPLASGIAVPTMILASEDDPIIPIGCLREADWPGHVELHTTRRGGHVGFIGGRQLETGDRYWMDAKLLNWFDCPQL

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Crispr_ID: NZ_CP036292_31

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036292_31

7238111-7238213

Orphan

Consensus_repeat	Method
TGGAAGCCGTATTAAAGTGACAATGCTGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036292_31

>merge|NZ_CP036292|31|7238111-7238213|CRISPRCasFinder
TGGAAGCCGTATTAAAGTGACAATGCTGCTTGCTCCTCCGTTGCGGATGAAGTGTTCGCATCACTTGGACACGTTGGAAGCCGTATTAAAGAGACAATGCTGC

>NZ_CP036292|31|30|7238111-7238213|CRISPRCasFinder
TGGAAGCCGTATTAAAGTGACAATGCTGC	TTGCTCCTCCGTTGCGGATGAAGTGTTCGCATCACTTGGACACGT
TGGAAGCCGTATTAAAGAGACAATGCTGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036292.1\|WP_145123910.1\|7225097_7226555_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|350123
NZ_CP036292.1\|WP_145123914.1\|7229655_7232247_-\|sulfatase-like-hydrolase/transferase	unknown	unknown	gnl\|CDD\|293749
NZ_CP036292.1\|WP_145123920.1\|7238723_7240007_-\|beta-ketoacyl-ACP-synthase-II	unknown	unknown	gnl\|CDD\|238430
NZ_CP036292.1\|WP_145123925.1\|7242910_7243660_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227042
NZ_CP036292.1\|WP_145123918.1\|7237051_7237861_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224117
NZ_CP036292.1\|WP_145123917.1\|7236305_7237028_-\|FHA-domain-containing-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145124349.1\|7232605_7233241_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP036292.1\|WP_145123916.1\|7234149_7236165_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP036292.1\|WP_145123911.1\|7226835_7227996_+\|PhnD/SsuA/transferrin-family-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270271
NZ_CP036292.1\|WP_145123913.1\|7228765_7229545_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|213260
NZ_CP036292.1\|WP_145123926.1\|7245394_7247524_-\|AMP-binding-protein	unknown	unknown	gnl\|CDD\|341254
NZ_CP036292.1\|WP_145123912.1\|7227995_7228769_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223673
NZ_CP036292.1\|WP_145123924.1\|7242545_7242956_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379111
NZ_CP036292.1\|WP_145123928.1\|7248524_7249235_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123915.1\|7233326_7234067_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123927.1\|7247720_7248455_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|225749
NZ_CP036292.1\|WP_145123921.1\|7240354_7240888_-\|beta-hydroxyacyl-ACP-dehydratase	unknown	unknown	gnl\|CDD\|238615
NZ_CP036292.1\|WP_145123922.1\|7241354_7241741_-\|acyl-carrier-protein	unknown	unknown	gnl\|CDD\|179197
NZ_CP036292.1\|WP_145123919.1\|7238453_7238663_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036292.1\|WP_145123923.1\|7241827_7242328_-\|beta-hydroxyacyl-ACP-dehydratase	unknown	unknown	gnl\|CDD\|238615

Protein	Function_ID	Function_description	E-value
NZ_CP036292.1\|WP_145123910.1\|7225097_7226555_-\|hypothetical-protein	gnl\|CDD\|350123	cd18611, GH130, Glycosyl hydrolase family 130; uncharacterized. This subfamily contains glycosyl hydrolase family 130 (GH130) proteins, as classified by the carbohydrate-active enzymes database (CAZY), most of which are as yet uncharacterized. GH130 enzymes are phosphorylases and hydrolases for beta-mannosides, and include beta-1,4-mannosylglucose phosphorylase (EC 2.4.1.281), beta-1,4-mannooligosaccharide phosphorylase (EC 2.4.1.319), beta-1,4-mannosyl-N-acetyl-glucosamine phosphorylase (EC 2.4.1.320), beta-1,2-mannobiose phosphorylase (EC 2.4.1.-), beta-1,2-oligomannan phosphorylase (EC 2.4.1.-) and beta-1,2-mannosidase (EC 3.2.1.-). They possess 5-bladed beta-propeller domains similar to families 32, 43, 62, 68, 117 (GH32, GH43, GH62, GH68, GH117). GH130 enzymes are involved in the bacterial utilization of mannans or N-linked glycans. Beta-1,4-mannosylglucose phosphorylase is involved in degradation of beta-1,4-D-mannosyl-N-acetyl-D-glucosamine linkages in the core of N-glycans; it produces alpha-mannose 1-phosphate and glucose from 4-O-beta-D-mannosyl-D-glucose and inorganic phosphate, using a critical catalytic Asp as a proton donor.	0.00759232
NZ_CP036292.1\|WP_145123914.1\|7229655_7232247_-\|sulfatase-like-hydrolase/transferase	gnl\|CDD\|293749	cd16025, PAS_like, Bacterial Arylsulfatase of Pseudomonas aeruginosa and related proteins. Sulfatases catalyze the hydrolysis of sulfate esters from wide range of substrates, including steroids, carbohydrates and proteins. Sulfate esters may be formed from various alcohols and amines. The biological roles of sulfatase includes the cycling of sulfur in the environment, in the degradation of sulfated glycosaminoglycans and glycolipids in the lysosome, and in remodeling sulfated glycosaminoglycans in the extracellular space. The sulfatases are essential for human metabolism. At least eight human monogenic diseases are caused by the deficiency of individual sulfatases.	0
NZ_CP036292.1\|WP_145123920.1\|7238723_7240007_-\|beta-ketoacyl-ACP-synthase-II	gnl\|CDD\|238430	cd00834, KAS_I_II, Beta-ketoacyl-acyl carrier protein (ACP) synthase (KAS), type I and II. KASs are responsible for the elongation steps in fatty acid biosynthesis. KASIII catalyses the initial condensation and KAS I and II catalyze further elongation steps by Claisen condensation of malonyl-acyl carrier protein (ACP) with acyl-ACP.	0
NZ_CP036292.1\|WP_145123925.1\|7242910_7243660_-\|hypothetical-protein	gnl\|CDD\|227042	COG4698, COG4698, Uncharacterized protein conserved in bacteria [Function unknown].	0.000641103
NZ_CP036292.1\|WP_145123923.1\|7241827_7242328_-\|beta-hydroxyacyl-ACP-dehydratase	gnl\|CDD\|238615	cd01288, FabZ, FabZ is a 17kD beta-hydroxyacyl-acyl carrier protein (ACP) dehydratase that primarily catalyzes the dehydration of beta-hydroxyacyl-ACP to trans-2-acyl-ACP, the third step in the elongation phase of the bacterial/ plastid, type II, fatty-acid biosynthesis pathway.	4.38345e-27
NZ_CP036292.1\|WP_145124349.1\|7232605_7233241_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	3.6076e-16
NZ_CP036292.1\|WP_145123916.1\|7234149_7236165_-\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.27865e-68
NZ_CP036292.1\|WP_145123911.1\|7226835_7227996_+\|PhnD/SsuA/transferrin-family-substrate-binding-protein	gnl\|CDD\|270271	cd13553, PBP2_NrtA_CpmA_like, Substrate binding domain of ABC-type nitrate/bicarbonate transporters, a member of the type 2 periplasmic binding fold superfamily. This subfamily includes nitrate (NrtA) and bicarbonate (CmpA) receptors. These domains are found in eubacterial perisplamic-binding 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 their ligand with high affinity, they 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. These binding 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.	2.60387e-60
NZ_CP036292.1\|WP_145123922.1\|7241354_7241741_-\|acyl-carrier-protein	gnl\|CDD\|179197	PRK00982, acpP, acyl carrier protein; Provisional.	7.57429e-15
NZ_CP036292.1\|WP_145123926.1\|7245394_7247524_-\|AMP-binding-protein	gnl\|CDD\|341254	cd05931, FAAL, Fatty acyl-AMP ligase (FAAL). FAAL belongs to the class I adenylate forming enzyme family and is homologous to fatty acyl-coenzyme A (CoA) ligases (FACLs). However, FAALs produce only the acyl adenylate and are unable to perform the thioester-forming reaction, while FACLs perform a two-step catalytic reaction; AMP ligation followed by CoA ligation using ATP and CoA as cofactors. FAALs have insertion motifs between the N-terminal and C-terminal subdomains that distinguish them from the FACLs. This insertion motif precludes the binding of CoA, thus preventing CoA ligation. It has been suggested that the acyl adenylates serve as substrates for multifunctional polyketide synthases to permit synthesis of complex lipids such as phthiocerol dimycocerosate, sulfolipids, mycolic acids, and mycobactin.	0
NZ_CP036292.1\|WP_145123912.1\|7227995_7228769_+\|ABC-transporter-permease-subunit	gnl\|CDD\|223673	COG0600, TauC, ABC-type nitrate/sulfonate/bicarbonate transport system, permease component [Inorganic ion transport and metabolism].	3.22876e-57
NZ_CP036292.1\|WP_145123924.1\|7242545_7242956_+\|hypothetical-protein	gnl\|CDD\|379111	pfam13298, LigD_N, DNA polymerase Ligase (LigD). This is the N terminal region of ATP dependant DNA ligase.	2.68223e-15
NZ_CP036292.1\|WP_145123927.1\|7247720_7248455_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|225749	COG3208, GrsT, Predicted thioesterase involved in non-ribosomal peptide biosynthesis [Secondary metabolites biosynthesis, transport, and catabolism].	9.47799e-51
NZ_CP036292.1\|WP_145123921.1\|7240354_7240888_-\|beta-hydroxyacyl-ACP-dehydratase	gnl\|CDD\|238615	cd01288, FabZ, FabZ is a 17kD beta-hydroxyacyl-acyl carrier protein (ACP) dehydratase that primarily catalyzes the dehydration of beta-hydroxyacyl-ACP to trans-2-acyl-ACP, the third step in the elongation phase of the bacterial/ plastid, type II, fatty-acid biosynthesis pathway.	2.24489e-33
NZ_CP036292.1\|WP_145123918.1\|7237051_7237861_-\|hypothetical-protein	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	0.00787767
NZ_CP036292.1\|WP_145123913.1\|7228765_7229545_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|213260	cd03293, ABC_NrtD_SsuB_transporters, ATP-binding cassette domain of the nitrate and sulfonate transporters. NrtD and SsuB are the ATP-binding subunits of the bacterial ABC-type nitrate and sulfonate transport systems, respectively. ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	5.53351e-119

>NZ_CP036292.1|WP_145123918.1|7237051_7237861_-|hypothetical-protein
MIKKTLVGGSLALLLSGLVFGTGMSSYMKTGFGYARDAVKDVVPVNVEIDRARQMIDDLQPEIAKNMKLIASEKIHVAKLQKQIDSKADMLASAERDIMRLTADLQSGDTRFVYAKRTYSADQVKDDLAGRFNRFKTQKATVDKLQQMLTAREKTLQAAKDRMDEMLSAKRQLEVEVENLQAQYAANQVAHAASSLNLDDSHLSRTRDLIDSIRTRIEVDEELLAVDNQYYGTIELTEESDEDILNQVSTYFNGDQPTAEDSVAMIQID
>NZ_CP036292.1|WP_145123917.1|7236305_7237028_-|FHA-domain-containing-protein
MTCGPVVNPTGLPSWNNEYLAGSTIEVNSVVEDRPHDRSHAQRGSDSKNARMLWIDGVGGFLIVAGDEWLIGGPGAGSSVEINVQGDLSRRAAAVRRQGSDYVLQPLASTRLQGEPLDRPTLLRTGDRFQLGSVVQFEFQKTHPLSSSARLNLVSRHRTQPRADGMILLADTCVIGPSQGAHIQCSHWTSDVILFVSGDDWRIRSEEPLVVDGTQIGQTAVLSSDCRIVGETLAMSMERL
>NZ_CP036292.1|WP_145123916.1|7234149_7236165_-|protein-kinase
MPALADKIESTRYAPNPLADEDLRKTGLTMKFTYATGDQPLKGYTIKRGIGVGGFGEVYFAVSGAGKEVALKRVQRNLDIELRGVGHCMNLKHPNLVALYDVKYDDNDQAWILMEYVAGATLRDELDRHRQGLPREQALRWFGDLAAGVAYLHDHGIVHRDLKPGNIFDDEGIFKIGDYGLSKFISCSRRGGNTESVGTFHYMAPEIGRGEYGKEIDIYALGIILFELLTGDVPFNGESSHEIIMKHLTSDPDLSQVEPPFRGVIAKALQKNPEARQKSVAELLEPLGMLLDKHGLAQLDPDAHARPILAELISDPATPHYAQQNNPRNNAAGPAMNSGPVHNAKKAPSEPLAFAVHKSAHDLNHWWHDRSANPLGRLIVVVVAVVILLMNSAWLLPMLSLLAMLYIPYYVIRTMVLTNQRQPSYAAAHAAAVNAQRRQQMTPTRQQWRMMARRELADKSLRTRAAELTESWATALIVLGVLGWVATMFGIAEGDGGARAIAPFAWGAATALAGAWLMLGLGKAWESDEAEGLPRRIVQLGVGAVVGAIAYGLGRGLMIPMDSGFDLDRVALDLPRHMYSGSGEILLPAMMAHFAAIFFLARWWRAADPLRARRMSIWSIAVVVVVAWLVNQVIPVPQPWGMLTAAAMVIAIQMAAVWKNPAHRIARVHGA
>NZ_CP036292.1|WP_145123915.1|7233326_7234067_-|hypothetical-protein
MLISKTKSPYLALLLATVFGFVMGVASSGIADEADEPKELSKVEAAADEKSDSKLEEKPESKVEPSEDDSQPHELSTAPLDYPIYPEDRPMWVDQPDKIGDDWAELVVQSVPSLSADSSRESLLQQQKIALIAYIDQALGFPGAGEKIAVPAEQIASGLVDPDRTYNGKLTTSTGEMFQHASVLVLDDDFHSEITQQWQALEVGQRLKGLGVLAALALVGLSGLTVLLKSISPRSKVGHDDKTALA
>NZ_CP036292.1|WP_145124349.1|7232605_7233241_-|sigma-70-family-RNA-polymerase-sigma-factor
MSETQANSLLVSRIREGDQRAWEDLIDRYEGRLLAFAESRIRNRAASEDIVQEAFIGFLTSLPNYDGARPLESYLFSICAYKLTDHLRREGRRPAISFSATGSQGSWDLAGTARPASSIARSGERRNLEETAVREALESQIKHWKQRGDWKKLRCLELLFVRGVGNKQVAEELNLNEQQVANYKSDFLLRVRTLVKRMNLDEEVFPELAGD
>NZ_CP036292.1|WP_145123914.1|7229655_7232247_-|sulfatase-like-hydrolase/transferase
MNKNCLRAVSRRLFPVFVVGMVMTSPGWSQDGSPPAAGRGGSNAGTAKSAFVPQVIGELGSPAATTTIDGKQLPAPAEKFGGKIKDNAAQSKAWWAPRIVPPKEAPNVLLIMTDDVGFGAPSTFGGVIPTPALDRIGKAGLRYTQFHSTSLCSPTRAALITGRNHHSAGFGVISEQSTGFPGYNSIIEKDKATIGRILKDNGYSTSWFGKDHNVPTFQASQVGPFDQWPIGMGFDYFYGFVGGDTSQWQPNLYRQTTPIYPYVDNPEWNLTTAQADDAIAKLNQLNQIDPTKPFFCYYVPGGTHAPHHATPEWIEKISDMHLFDEGWNELRKTIFANQKKLGVIPADAKLTPWPDDLLKHWDELTADEKKLFIRQVEVYAAYLAYTDHEIGRVIQAVEDMGKLDDTLIIYISGDNGGSVEGTQVGTPNEVAAFNGVEVPVELQLEKFYDVWGSDQTYNHMAVPWSWSFCTPYSWTKQVASHLGGVRQGMCVSWPAKIKDAGGIRHQFHHVIDVVPTILETAGIAAPEEVDGIPQKPIEGVSFAYTFDESNANAPSTHKTQYFEMMGDHAIYHEGWMASTKVVRPPWEIVGAVNQDPVNNVTWELFDLTKDWTQSNDIAAEHPEKLEELKALFLEEARKYQVLPLDATVATRLVAPRPNITAGRTEFTYTQPMTGVPQGDSPVLINCSYSITADIEVPENGAEGMLLTSGGRFGGYGFYLLKGKPVFLWNLVDLKRQRWEGPDALAPGKHVLEFEFTYDGMGMGTLAFNNLSGIGQSGIGVLKVDGKEVATGKLPHTIPLILQWDETFDIGSDTGTPVDDKDYKTPFEFTGKLNKLTLELQRPNLSPADIRKLEAAQRNNKASE
>NZ_CP036292.1|WP_145123913.1|7228765_7229545_+|ATP-binding-cassette-domain-containing-protein
MTQPTPKIELRDLQLEYSGRDGAVMPVLQSIDLTVREGEFICIVGPSGCGKSTLLNIACGFLQPTRGQVLIDGTVVQRPDRRRVFIFQNNAVFPWLTVQQNIGFGLLDQSPKERDEAVRHYTEMVGLTGFEQAYPRELSGGMNQRVEIARALAADPDVLYMDEPLGALDFLTRLKMRTDLVEIWRRTQKTILFVTHDVEESVQLADRVVVMSPRPAEIRAILDVDLPRPRNLDSPEYLAIRDKIFRTMGLDHSGMQAEA
>NZ_CP036292.1|WP_145123912.1|7227995_7228769_+|ABC-transporter-permease-subunit
MLARKILLGTLGIGIFLLIWHLATLGNSRTDVPGPWLAFNGLIELAGQGVLWRYVIASVFRVAWGFFLAAIVGIPLGLAIGWSLWIRELLNPLVQALRPISPIAWLPIAVLVFGGVQWWEPSDLAAIFLIFLASLFPIVTAATSSVGAIDEKYLRAAENFGVRGLPLLRLVILPAALPQILTGLRLAMGIAWVVVVAAEMLGVQSGLGFQINDSRNNLRYDFVVAAMLVISVIGMLLDAAMSRIERTSLARTGMARR
>NZ_CP036292.1|WP_145123911.1|7226835_7227996_+|PhnD/SsuA/transferrin-family-substrate-binding-protein
MSSVGKLALSCLCLLGTVTILHAHFNLGMFDRPQHIAGDENGAVRKSLRVGHLPVTCHLTCPVTSWVSKHSQQHSEFVSWRYTSWPAMTEDIDAGNLDAAFILAPLAMVMQRQGTPVKIVHLGHRDGTAIVVNKDSPYKTFADLRGKRIAIPHRYSNQRILIEKLKDEFGLTNAEITLIDYPPPEMPAGLKSGQFEAYIVGEPFAAKAEMDGFGRVLYFTKDIWPNFISCVLVVTERLIERDPELVTELVQGISASGKWIDQGDDRLMAGLAVEGTPSADGDAIPEQFGRSPRMQAAWIAARQEYYNQDPELLKFVLTRPLDRVSYSRLDLAREDFAEIQDYAQRLGFFSFRPVTADDPFGFDDYCDPSFEQSGMWSLPLESEEPQ
>NZ_CP036292.1|WP_145123910.1|7225097_7226555_-|hypothetical-protein
MRYPRNRMLPALVILASLTASNHAAEPLMLGSRWELFVDEYLIDSKQNVELKLHEPVRREIVLTTDKPWEGPTSAYFSVVQDGEKVRLYYRGSDGGPDHSESQFTCVAESEDGIHFTRPKLGLIEAGGTKENNVIWRGVESHNFAPFLDANPSAKPDARFKALGGVKMPGKNWQYGDTPGGLYAFASADGIHWRKLQKEPVITKGAFDSQNLAFWDAARNRYACFSRIFSVEDQLRAIQSSHSQDFLKWSTGVPHRYAEDAPKEHFYTSATIPCPTAPHLFLSFPKRFQPARRKIPEHSVKGVSDTIFMSSRDGVHWDRPFLQAWARPGLDPKNWTDRSNMVAYGIYDGGDGEWSLYISEHYRHADHRIRRLTVRQQGFASAHVGGGKHGEFTTHPIQFDGDSLQLNYASSAAGSIQIEIQDEKGQPIPGFTMQEMPELFGDELAATATWNSGSDLSSLRGKTIRLRVKMIDADLYALRFTDNVK
>NZ_CP036292.1|WP_145123919.1|7238453_7238663_+|hypothetical-protein
MSPIYSNPKNGTATTLPIEATWAELSERTDKSDTSALAQWIEADLERIENQLSDFITPNTLKKSLRSGR
>NZ_CP036292.1|WP_145123920.1|7238723_7240007_-|beta-ketoacyl-ACP-synthase-II
MRPRVVVTGIGMINPMGHDPTTVWKGLQEGQSGVGYTTLFNAKGFPTQISAEVKGWDITDTGEDPELWKHRGRHTKFAAGAAKQAISESGIMDAGVAPHRFGVYLGSGEGNQDFVTFTDMMTVAMEGGEYDMAKFLQKGLEVLNPLVELEQEPNMPAAHLAAMFNAQGPNYNCLTACAASSQAIGEATEIIRRGDADVMLSGGTHSMIHPFGVTGFNLLTALSENNANPTAASRPFDARRDGFVLGEGSGMVVLEELEHARRRGAPIYGEILGYGTTADAFRITDIPPDGHGGIASMRMAISDAGLNPEDIDYVNAHGTSTTVNDKVETLACKQVFGDNAYKTPVSSTKSMMGHLIAAAGVTEMIVCLLAIRDSVLPPTINYENPDPLCDLDYVPNEARQAKVKYALNNSFGFGGQNVTLCLGKFEA
>NZ_CP036292.1|WP_145123921.1|7240354_7240888_-|beta-hydroxyacyl-ACP-dehydratase
MRWFWIDRFTYFKSRERAEAIKNISLTEEPVDEYLPAHPVFPNTLIIEGLAQTGGILVSECFDFQQRIVLAKVGKAKFHQPARPGDTLHYTATIDDLQNDGAVITGTSYCEGKLQAEVQMLFAFLDEERFGTGQLFNPANLLTMLRLMRLWEVAQDADGNPLPVSKNLLDDESTPAT
>NZ_CP036292.1|WP_145123922.1|7241354_7241741_-|acyl-carrier-protein
MPTQDEVYEKVQAALVDALGVDDDEVTPEATMVGDLGAESIDFLDIVFKLEKAFDIQIPREELFPEDILTNSEYVKDGKVTEDGLVELKKRMSWADLSKFEKNPRVQDFGDLLTVNDLCSYVNSKVGA
>NZ_CP036292.1|WP_145123923.1|7241827_7242328_-|beta-hydroxyacyl-ACP-dehydratase
MRYSQLDEIVALQPGIQLIARRTLHASEDYLLDHFPRFPVMPGVMMLEALYQAAMWMVRTGEDFASPHVFLVEAKSVKFGDFLCPGETLEIKADKFKEDGPLVTVKAQATKGDKVTVSARLILERSGSEASPHNNDDDTRRFVREQFFNMFGDQPAVIQAMTQSTL
>NZ_CP036292.1|WP_145123924.1|7242545_7242956_+|hypothetical-protein
MNEDSLSSAATASNFVLLWHQLPASSPRRSHFDLMLEDSGQLRTWAIPRIPSPGESVQGLGLPPHRIAYLDLEGEISGGRGSVRRIDRGTYTIIESSDEQLSIEIRGDQLTGQLRFRATESDQLWEISRVDALANL
>NZ_CP036292.1|WP_145123925.1|7242910_7243660_-|hypothetical-protein
MRRLLKTLGLVLVFIATGLGAFTWWAARAAQQAPAFYKTAVASAPLALQHKEELQAQFEQLSQQVQIVGDWHATFTTDQINAWLASELANQFPNVLPPGTEDPRVSVEDGKVIVAARYRRGRIDSVISFELHAQLTDEPNVIALQIHRLRAGALPIPLQHFSDKISIAASRGDLEVRWENEEDDLIALVTVPSEHDRYVETPVVIETLELLDGEIVLAGRTGAKAHTAWIPDGPIYKLAKASTREISHN
>NZ_CP036292.1|WP_145123926.1|7245394_7247524_-|AMP-binding-protein
MISSHKNMSLPQETTQRHGGWRSLTELMVDRSRRHPDRAVATFLTDAGESQSITYGQLDRRARSVAAELAQCTTPGDRALLLFPPGLEFLVGFFGASYAGLVPVPTCFPKPGRAMPRLDTAAVDCQPAALIADRETLEGLDFKRLNEVVHKTHRIATDGVAAVDFDPHIDDGSGEALGLLQYTSGSTSDPKGVMVRNANLLSNLESIRSSYALEFAADDASEHSRGVFWLPAYHDMGLIGGILEPIYVGGEAVLMSPRSFLQRPLRWLQAISSHRASFSGAPNFAYQLCVDRIDPEHTRGLDLSCWTTAFCGAEPVRAATLEAFIQRFEPAGYRASSFCPCYGLAEATLLAAGGGDRNEPKYLDVDRDSLSVGRYQPAAEGQPEATVQRLVSSGPAADGMRIAIVDPDTAAAQADGAVGEIWLQGPSVADGYWNREAVNAEQFHATIAGEPEAGKFLRSGDLGFLHRDQLYVTGRMKDVIILRGRNVYPQDIEATVCECLGEASGGPAAAFSAQGDGQEALAVVAEVARQTPPESLAGLVRRLRRRLIEQHEVDARTIALTRPGGVPLTTSGKVQRQACRRQFFSGELKTKHRWDRSIMLGGNVEFPELPTTITPDDLPAVSAAIEGWLLEWLAARGNPDNGPADRDKPLADYGLDSLATMELAGDVEDWLGLELTPTLAWDYPTPAVLAPHLAENMLETGPDETARER
>NZ_CP036292.1|WP_145123927.1|7247720_7248455_+|alpha/beta-fold-hydrolase
MFRTIYEAAEPKLQFFWFCHAGAGSASLVRAARGLSGPLSLQVASLPGREHRFRDGLNLSLDELVDQLAAELRAQIRGPYHLIGHSFGSLLSYLLAQKMIAAGLPPLSLTVMTLAAPDRVNRNPRTAHLSNEEFLDYLDHRFGSVPRALRTNPEAAALFLPIVRYDLQLLESYVHQPTPPLPIPILALAGSDDRAVSPEAMRQWERFTSESFELQTIPGGHFFPTENVEPIIQRAIGAFQQGPS
>NZ_CP036292.1|WP_145123928.1|7248524_7249235_+|hypothetical-protein
MTASPSPVSKSRSPIVWIITAIVLLVVGLFGCLILWLASGVSGREFAPSHFQTRTFNVASVPWIGFQIGSLDHSSVNDATSQYLIANKLINVPATPPKRWDLLEIHRNVSLPHDADASVLTLYLTGRGSHGVDWEQWSKDHPAAAAVFWPFVQQLAIDQLYLMLPQAFDLARQQTDPVELQQALDDYFVAEFPAFAADLAHAGREAEAIAALESAIDRYPQQASFSAALDDLQSQK

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP036292_13	13.1\|2999496\|17\|NZ_CP036292\|CRISPRCasFinder	2999496-2999512	17	NZ_CP036292.1	2999403-2999419	0	1.0
NZ_CP036292_22	22.1\|5447635\|18\|NZ_CP036292\|CRT	5447635-5447652	18	NZ_CP036292.1	6589651-6589668	0	1.0
NZ_CP036292_17	17.1\|4360235\|29\|NZ_CP036292\|CRISPRCasFinder	4360235-4360263	29	NZ_CP036292.1	4360424-4360452	1	0.966
NZ_CP036292_22	22.1\|5447635\|18\|NZ_CP036292\|CRT	5447635-5447652	18	NZ_CP036292.1	4419721-4419738	1	0.944
NZ_CP036292_22	22.1\|5447635\|18\|NZ_CP036292\|CRT	5447635-5447652	18	NZ_CP036292.1	4419748-4419765	1	0.944
NZ_CP036292_22	22.1\|5447635\|18\|NZ_CP036292\|CRT	5447635-5447652	18	NZ_CP036292.1	6589603-6589620	1	0.944
NZ_CP036292_22	22.1\|5447635\|18\|NZ_CP036292\|CRT	5447635-5447652	18	NZ_CP036292.1	6589627-6589644	1	0.944
NZ_CP036292_3	3.1\|196128\|34\|NZ_CP036292\|CRISPRCasFinder	196128-196161	34	NZ_CP036292.1	4212961-4212994	2	0.941
NZ_CP036292_3	3.1\|196128\|34\|NZ_CP036292\|CRISPRCasFinder	196128-196161	34	NZ_CP036292.1	5374928-5374961	2	0.941
NZ_CP036292_3	3.1\|196128\|34\|NZ_CP036292\|CRISPRCasFinder	196128-196161	34	NZ_CP036292.1	5758359-5758392	2	0.941

1. spacer 13.1|2999496|17|NZ_CP036292|CRISPRCasFinder matches to position: 2999403-2999419, mismatch: 0, identity: 1.0

caaaacgattcgtagtg	CRISPR spacer
caaaacgattcgtagtg	Protospacer
*****************

2. spacer 22.1|5447635|18|NZ_CP036292|CRT matches to position: 6589651-6589668, mismatch: 0, identity: 1.0

gcccatgccgcccatgcc	CRISPR spacer
gcccatgccgcccatgcc	Protospacer
******************

3. spacer 17.1|4360235|29|NZ_CP036292|CRISPRCasFinder matches to position: 4360424-4360452, mismatch: 1, identity: 0.966

accgcaagctggctcgaagccacatgctg	CRISPR spacer
accgcaagctggctcgatgccacatgctg	Protospacer
***************** ***********

4. spacer 22.1|5447635|18|NZ_CP036292|CRT matches to position: 4419721-4419738, mismatch: 1, identity: 0.944

gcccatgccgcccatgcc	CRISPR spacer
gcccattccgcccatgcc	Protospacer
****** ***********

5. spacer 22.1|5447635|18|NZ_CP036292|CRT matches to position: 4419748-4419765, mismatch: 1, identity: 0.944

gcccatgccgcccatgcc	CRISPR spacer
gcccattccgcccatgcc	Protospacer
****** ***********

6. spacer 22.1|5447635|18|NZ_CP036292|CRT matches to position: 6589603-6589620, mismatch: 1, identity: 0.944

gcccatgccgcccatgcc	CRISPR spacer
gcccatgccgcccatacc	Protospacer
***************.**

7. spacer 22.1|5447635|18|NZ_CP036292|CRT matches to position: 6589627-6589644, mismatch: 1, identity: 0.944

gcccatgccgcccatgcc	CRISPR spacer
gcccatgccacccatgcc	Protospacer
*********.********

8. spacer 3.1|196128|34|NZ_CP036292|CRISPRCasFinder matches to position: 4212961-4212994, mismatch: 2, identity: 0.941

aagatggtagccggaggtcgccgcacagcggcgc	CRISPR spacer
aagatggtagccggaggtcgtcgcgcagcggcgc	Protospacer
********************.***.*********

9. spacer 3.1|196128|34|NZ_CP036292|CRISPRCasFinder matches to position: 5374928-5374961, mismatch: 2, identity: 0.941

aagatggtagccggaggtcgccgcacagcggcgc	CRISPR spacer
aagatggtagccggaggtcgtcgcgcagcggcgc	Protospacer
********************.***.*********

10. spacer 3.1|196128|34|NZ_CP036292|CRISPRCasFinder matches to position: 5758359-5758392, mismatch: 2, identity: 0.941

aagatggtagccggaggtcgccgcacagcggcgc	CRISPR spacer
aagatggtagccggaggtcgtcgcgcagcggcgc	Protospacer
********************.***.*********

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP015073	Escherichia coli strain Ecol_743 plasmid pEC743_4, complete sequence	16602-16631	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_KM670336	Salmonella enterica subsp. enterica serovar Senftenberg strain SRC119 plasmid pSRC119-A/C, complete sequence	145378-145407	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP045255	Proteus mirabilis strain L90-1 plasmid pL902, complete sequence	14593-14622	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN543575	Klebsiella pneumoniae strain GH44TC plasmid pGH44TC_fusion, complete sequence	23690-23719	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	AP018710	Uncultured bacterium plasmid pSN1216-29 DNA, complete sequence	24742-24771	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP047338	Klebsiella pneumoniae strain 2019036D plasmid p2019036D-50kb, complete sequence	20517-20546	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP020602	Pseudomonas aeruginosa strain E6130952 plasmid pJHX613, complete sequence	25744-25773	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_MK262712	Klebsiella pneumoniae strain KP18-29 plasmid p18-29-MDR, complete sequence	156376-156405	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_MF174859	Escherichia coli strain 6/14/6b plasmid pIncHI2-MU3, complete sequence	93610-93639	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP014764	Klebsiella pneumoniae strain KPNIH39 plasmid pKPN-704, complete sequence	184-213	3	0.9
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR745047	Klebsiella pneumoniae isolate Kpn2166 plasmid pCTX-M15_Kpn2166	22749-22778	3	0.9
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT740732	Ralstonia phage Darius, complete genome	25005-25031	3	0.889
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT361768	Ralstonia phage RPZH6, complete genome	48437-48463	3	0.889
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT740740	Ralstonia phage Gervaise, complete genome	24381-24407	3	0.889
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP029835	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence	43598-43624	3	0.889
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP019083	Paludisphaera borealis strain PX4 plasmid PALBO1, complete sequence	80700-80726	3	0.889
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP010410	Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence	238253-238279	3	0.889
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN693998	Marine virus AFVG_250M48, complete genome	15177-15206	4	0.867
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_016588	Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence	80108-80137	4	0.867
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_021289	Burkholderia insecticola plasmid p1, complete sequence	782125-782154	4	0.867
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LN832562	Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence	253984-254013	4	0.867
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	893524-893550	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH590593	Mycobacterium phage Rabinovish, complete genome	73461-73487	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX781992	Mycobacterium phage Gabriel, complete genome	71107-71133	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH697579	Mycobacterium phage Cane17, complete genome	73743-73769	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112554	Mycobacterium phage TinyTim, complete genome	72603-72629	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359314	Mycobacterium phage Ewok, complete genome	72230-72256	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359337	Mycobacterium phage Flabslab, complete genome	70412-70438	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN234193	Mycobacterium phage Kboogie, complete genome	71810-71836	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450432	Mycobacterium phage ValleyTerrace, complete genome	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH051261	Mycobacterium phage Tyke, complete genome	73258-73284	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH779502	Mycobacterium phage FudgeTart, complete genome	71883-71909	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359365	Mycobacterium phage Loanshark, complete genome	72720-72746	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359311	Mycobacterium phage SmallFry, complete genome	71362-71388	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359364	Mycobacterium phage ChickenPhender, complete genome	71070-71096	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359303	Mycobacterium phage Shnickers, complete genome	72137-72163	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH697586	Mycobacterium phage InigoMontoya, complete genome	71821-71847	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112549	Mycobacterium phage Morizzled23, complete genome	72215-72241	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112541	Mycobacterium phage Jessibeth14, complete genome	72649-72675	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359347	Mycobacterium phage Ading, complete genome	72119-72145	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450425	Mycobacterium phage Shelob, complete genome	73645-73671	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_023714	Mycobacterium phage LinStu, complete genome	72704-72730	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359358	Mycobacterium phage Essence, complete genome	71701-71727	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KJ595575	Mycobacterium phage Willis, complete genome	72748-72774	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MG812493	Mycobacterium phage NuevoMundo, complete genome	75118-75144	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359339	Mycobacterium phage Naija, complete genome	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359333	Mycobacterium phage JustHall, complete genome	72645-72671	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KT321476	Mycobacterium phage Zeenon, complete genome	72608-72634	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN428065	Mycobacterium phage Cactojaque, complete genome	71430-71456	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359306	Mycobacterium phage Norm, complete genome	73538-73564	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN735434	Mycobacterium phage Mangeria, complete genome	72906-72932	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JN699625	Mycobacterium phage Wally, complete genome	71381-71407	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	EU826471	Mycobacterium phage Cali, complete genome	72881-72907	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX721255	Mycobacterium phage Yucca, complete genome	72522-72548	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359366	Mycobacterium phage Basquiat, complete genome	71438-71464	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359346	Mycobacterium phage NoodleTree, complete genome	72936-72962	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JN699013	Mycobacterium phage Pio, complete genome	74738-74764	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359361	Mycobacterium phage Darko, complete genome	72544-72570	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_023725	Mycobacterium phage Nappy, complete genome	73776-73802	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359348	Mycobacterium phage Rahel, complete genome	71738-71764	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH779498	Mycobacterium phage Bread, complete genome	72370-72396	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450427	Mycobacterium phage Adlitam, complete genome	72615-72641	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MG812494	Mycobacterium phage Pier, complete genome	75126-75152	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	GQ303262	Mycobacterium phage LRRHood, complete genome	72095-72121	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT818423	Mycobacterium phage Janiyra, complete genome	72787-72813	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH316567	Mycobacterium phage ParkTD, complete genome	72849-72875	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	AY129337	Mycobacteriophage Bxz1, complete genome	74082-74108	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH051260	Mycobacterium phage InterFolia, complete genome	74112-74138	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX721256	Mycobacterium phage Erdmann, complete genome	72853-72879	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359328	Mycobacterium phage EmmaElysia, complete genome	72079-72105	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KM881426	Mycobacterium phage ZygoTaiga	73768-73794	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359335	Mycobacterium phage Patter, complete genome	71877-71903	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT889395	Mycobacterium phage Shifa, complete genome	71069-71095	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	EU826467	Mycobacterium phage Rizal, complete genome	70886-70912	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT723944	Mycobacterium phage ChaylaJr, complete genome	71246-71272	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KR080196	Mycobacterium phage Momo, complete genome	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH910040	Mycobacterium phage Sauce, complete genome	71793-71819	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF919495	Mycobacterium phage Bigswole, complete genome	74095-74121	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359318	Mycobacterium phage Specks, complete genome	74027-74053	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KF024734	Mycobacterium phage Shrimp, complete genome	72857-72883	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112548	Mycobacterium phage McWolfish, complete genome	72625-72651	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359308	Mycobacterium phage Shaqnato, complete genome	70843-70869	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112545	Mycobacterium phage Khaleesi, complete genome	72752-72778	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH825697	Mycobacterium phage Bangla1971, complete genome	71829-71855	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359338	Mycobacterium phage Amataga, complete genome	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359350	Mycobacterium phage Nidhogg, complete genome	73066-73092	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT723945	Mycobacterium phage Quasimodo, complete genome	73277-73303	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359342	Mycobacterium phage ShiaLabeouf, complete genome	72173-72199	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH316561	Mycobacterium phage Derek, complete genome	72471-72497	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112533	Mycobacterium phage Bonray, complete genome	73194-73220	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450422	Mycobacterium phage RoMag, complete genome	72050-72076	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359327	Mycobacterium phage EmToTheThree, complete genome	73804-73830	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH727543	Mycobacterium phage CharlieB, complete genome	71764-71790	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JF704116	Mycobacterium phage Drazdys, complete genome	71535-71561	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359336	Mycobacterium phage Chargie21, complete genome	71438-71464	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359355	Mycobacterium phage Sprinklers, complete genome	71418-71444	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112534	Mycobacterium phage Burrough, complete genome	72879-72905	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF919499	Mycobacterium phage Daffodil, complete genome	72852-72878	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359334	Mycobacterium phage Delilah, complete genome	73006-73032	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_023696	Mycobacterium phage Dandelion, complete genome	75044-75070	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN276192	Mycobacterium phage Trinitium, complete genome	71786-71812	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359324	Mycobacterium phage Tortoise16, complete genome	71962-71988	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH825713	Mycobacterium phage Zalkecks, complete genome	72523-72549	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359349	Mycobacterium phage FoxtrotP1, complete genome	74013-74039	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JF704096	Mycobacterium phage Ghost, complete sequence	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN062707	Mycobacterium phage Grungle, complete genome	69125-69151	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359344	Mycobacterium phage Napoleon13, complete genome	70413-70439	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH727558	Mycobacterium phage Salacia, complete genome	73177-73203	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359363	Mycobacterium phage Fludd, complete genome	71878-71904	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX831080	Mycobacterium phage Lukilu, complete genome	73105-73131	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359329	Mycobacterium phage Kamryn, complete genome	73455-73481	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JQ911768	Mycobacterium phage Ava3, complete genome	72284-72310	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_004687	Mycobacterium phage Bxz1, complete genome	74082-74108	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_011270	Mycobacterium phage Spud, complete genome	72923-72949	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN183280	Mycobacteriophage LolaVinca, complete genome	73063-73089	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359345	Mycobacterium phage QBert, complete genome	71853-71879	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	GQ303260	Mycobacterium phage ET08, complete genome	71525-71551	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH744422	Mycobacterium phage Roots515, complete genome	73515-73541	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359321	Mycobacterium phage Phusco, complete genome	72136-72162	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359362	Mycobacterium phage Atlantean, complete genome	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	EU826469	Mycobacterium phage ScottMcG, complete genome	71799-71825	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK310143	Mycobacterium phage Dietrick, complete genome	70547-70573	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450429	Mycobacterium phage Bipolarisk, complete genome	72552-72578	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH051266	Mycobacterium phage MikeLiesIn, complete genome	72866-72892	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_029044	Mycobacterium phage Breeniome, complete genome	70728-70754	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK494105	Mycobacterium phage Pinnie, complete genome	24888-24914	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH669008	Mycobacterium phage Megamind, complete genome	72509-72535	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK878897	Mycobacterium phage Blackbrain, complete genome	71323-71349	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450434	Mycobacterium phage DrPhinkDaddy, complete genome	73064-73090	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359359	Mycobacterium phage Colt, complete genome	73860-73886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF919527	Mycobacterium phage Phox, complete genome	73129-73155	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT818416	Mycobacterium phage BackyardAgain, complete genome	71287-71313	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359330	Mycobacterium phage Iota, complete genome	71809-71835	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KT365398	Mycobacterium phage DTDevon, complete genome	72911-72937	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX369583	Mycobacterium phage Littleton, complete genome	72189-72215	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF919494	Mycobacterium phage BeanWater, complete genome	72138-72164	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_028869	Mycobacterium phage HyRo, complete genome	71803-71829	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KT365400	Mycobacterium phage ErnieJ, complete genome	70822-70848	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KC691257	Mycobacterium phage Astraea, complete genome	71140-71166	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MG872839	Mycobacterium phage LifeSavor, complete genome	72069-72095	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KC748968	Mycobacterium phage Gizmo, complete genome	74482-74508	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KC748970	Mycobacterium phage ArcherS7, complete genome	71699-71725	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359353	Mycobacterium phage BadAgartude, complete genome	72586-72612	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH697590	Mycobacterium phage Phlegm, complete genome	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359317	Mycobacterium phage FrayBell, complete genome	73177-73203	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT553335	Mycobacterium phage Ronan, complete genome	69999-70025	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN428066	Mycobacterium phage JPickles, complete genome	70612-70638	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359305	Mycobacterium phage Teardrop, complete genome	71351-71377	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	DQ398053	Mycobacteriophage Catera, complete genome	71145-71171	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF919513	Mycobacterium phage Koguma, complete genome	70287-70313	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JN699626	Mycobacterium phage MoMoMixon, complete genome	72342-72368	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_028986	Mycobacterium phage Alice, complete sequence	71840-71866	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450424	Mycobacterium phage Melpomini, complete genome	69975-70001	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JN204348	Mycobacterium phage Sebata, complete genome	73262-73288	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN183285	Mycobacterium phage YoungMoneyMata, complete genome	72486-72512	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK450423	Mycobacterium phage Stubby, complete genome	71385-71411	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF919493	Mycobacterium phage Audrick, complete genome	71839-71865	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_008207	Mycobacterium phage Catera, complete genome	71145-71171	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JN624850	Mycobacterium phage Pleione, complete genome	73016-73042	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK359326	Mycobacterium phage Pivoine, complete genome	71860-71886	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP023066	Sinorhizobium sp. CCBAU 05631 plasmid pSS05631d, complete sequence	67608-67634	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP025114	Bradyrhizobium sp. SK17 strain CBNU plasmid unnamed, complete sequence	22299-22325	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP025114	Bradyrhizobium sp. SK17 strain CBNU plasmid unnamed, complete sequence	285030-285056	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP021126	Rhizobium sp. Kim5 plasmid pRetKim5b, complete sequence	448072-448098	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP013516	Rhizobium sp. N1314 plasmid pRspN1314e, complete sequence	439263-439289	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP054029	Rhizobium sp. JKLM19E plasmid pPR19E02, complete sequence	190089-190115	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	735596-735622	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1551363-1551389	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP015231	Epibacterium mobile F1926 plasmid unnamed1, complete sequence	832149-832175	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP054613	Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence	531430-531456	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH697583	Mycobacterium phage EricMillard, complete genome	23995-24021	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH727551	Mycobacterium phage Kalah2, complete genome	24310-24336	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF919504	Mycobacterium phage DmpstrDiver, complete genome	23864-23890	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH669017	Mycobacterium phage Zelink, complete genome	23873-23899	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN062701	Mycobacterium phage Dallas, complete genome	23231-23257	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK524527	Mycobacterium phage ThreeRngTarjay, complete genome	23845-23871	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK524529	Mycobacterium phage Phoebus, complete genome	23995-24021	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK524504	Mycobacterium phage Hughesyang, complete genome	23878-23904	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP013104	Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence	4847-4873	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_LR134456	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence	219457-219483	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	2075946-2075972	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	285319-285345	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP014769	Hymenobacter sp. PAMC 26554 plasmid unnamed1, complete sequence	30992-31018	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP025432	Paracoccus zhejiangensis strain J6 plasmid pPZ02, complete sequence	29143-29169	4	0.852
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP017563	Paraburkholderia sprentiae WSM5005 plasmid pl1WSM5005, complete sequence	164394-164420	4	0.852
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP029357	Azospirillum sp. CFH 70021 plasmid unnamed2	650104-650133	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR134456	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence	185387-185416	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1751220-1751249	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP016619	Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence	832777-832806	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP016620	Microvirga ossetica strain V5/3m plasmid unnamed4, complete sequence	466578-466607	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK279905	Mycobacterium phage Acquire49, complete genome	67787-67816	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MF185726	Mycobacterium phage Appletree2, complete genome	67843-67872	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK310144	Mycobacterium phage CicholasNage, complete genome	68132-68161	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MH744425	Mycobacterium phage Wamburgrxpress, complete genome	68398-68427	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	JN600672	Mycobacterium phage Fezzik, complete genome	68221-68250	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN586018	Mycobacterium phage Wyatt2, complete genome	68159-68188	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN096382	Mycobacterium phage AvadaKedavra, complete genome	67901-67930	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK494100	Mycobacterium phage Halena, complete genome	67775-67804	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	JF704113	Mycobacterium phage UPIE, complete sequence	67732-67761	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_042313	Mycobacterium virus JoeDirt, complete genome	69006-69035	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	HM152763	Mycobacterium virus Bron, complete genome	67406-67435	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN586023	Mycobacterium phage Zaria, complete genome	68467-68496	5	0.833
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MT771349	Mycobacterium phage Tyson, complete genome	68495-68524	5	0.833
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP026093	Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence	693431-693457	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP011053	Halomonas sp. KO116 plasmid unnamed1, complete sequence	22716-22742	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN693998	Marine virus AFVG_250M48, complete genome	14623-14649	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP017244	Rhizobium etli 8C-3 plasmid pRsp8C3c, complete sequence	851513-851539	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	962156-962182	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP017105	Rhizobium gallicum strain IE4872 plasmid pRgalIE4872d, complete sequence	1292416-1292442	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	CP006880	Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence	1451980-1452006	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT310895	Arthrobacter phage StevieBAY, complete genome	31285-31311	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP048636	Rhizobium oryzihabitans strain M15 plasmid p4, complete sequence	29308-29334	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK284518	Mycobacterium phage ACFishhook, complete genome	4391-4417	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK279903	Mycobacterium phage Zetzy, complete genome	3834-3860	5	0.815
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_031074	Gordonia phage Bantam, complete genome	56551-56577	5	0.815
NZ_CP036292_17	17.1\|4360235\|29\|NZ_CP036292\|CRISPRCasFinder	4360235-4360263	29	NC_020894	Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence	82413-82441	6	0.793
NZ_CP036292_17	17.1\|4360235\|29\|NZ_CP036292\|CRISPRCasFinder	4360235-4360263	29	NC_017766	Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence	82414-82442	6	0.793
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_016626	Burkholderia sp. YI23 plasmid byi_1p, complete sequence	201101-201130	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP024310	Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence	667739-667768	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP023064	Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence	488175-488204	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	677990-678019	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1403217-1403246	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP005085	Sphingobium sp. TKS plasmid pTK1, complete sequence	290388-290417	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	1694415-1694444	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP038257	Microbacterium sediminis strain YLB-01 plasmid unnamed, complete sequence	59581-59610	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	KU958700	Streptomyces phage Chymera, complete genome	33577-33606	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP020911	Rhizobium etli strain NXC12 plasmid pRetNXC12e, complete sequence	955126-955155	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_021911	Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1f, complete sequence	1059284-1059313	6	0.8
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK637516	Agrobacterium phage Milano, complete genome	17142-17171	6	0.8
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP030841	Acidisarcina polymorpha strain SBC82 plasmid pACPOL1, complete sequence	33895-33921	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF377441	Arthrobacter phage Timinator, complete genome	31290-31316	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KU647629	Arthrobacter phage BarretLemon, complete genome	31288-31314	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN693999	Marine virus AFVG_250M363, complete genome	18762-18788	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_049468	Arthrobacter phage Zartrosa, complete genome	31124-31150	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1814413-1814439	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_009717	Xanthobacter autotrophicus Py2 plasmid pXAUT01, complete sequence	49200-49226	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP012940	Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence	1495060-1495086	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP031599	Roseovarius indicus strain DSM 26383 plasmid pRIdsm_01, complete sequence	273005-273031	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP043477	Xanthomonas hyacinthi strain CFBP 1156 plasmid unnamed, complete sequence	20031-20057	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP021373	Rhizobium sp. ACO-34A plasmid pRACO34Ac, complete sequence	493410-493436	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_017966	Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence	372801-372827	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	388952-388978	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP051295	Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence	1480615-1480641	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_019202	Pseudomonas aeruginosa plasmid pKLC102, complete sequence	68055-68081	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP025188	Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence	307396-307422	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP032156	Mycobacterium sp. ELW1 plasmid pELW1-1, complete sequence	144611-144637	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MG925355	Mycobacterium phage OlanP, complete genome	4490-4516	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK112543	Mycobacterium Phage Kalb97, complete genome	4308-4334	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK967399	Mycobacterium phage Groupthink, complete genome	4310-4336	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX523125	Mycobacterium phage BuzzBuzz, complete genome	4359-4385	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KC661272	Mycobacterium phage Methuselah, complete genome	4358-4384	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MG925341	Mycobacteriophage EpicPhail, complete genome	4275-4301	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	JF704114	Mycobacterium phage Vix, complete genome	4357-4383	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK279913	Mycobacterium phage PotatoSplit, complete genome	4275-4301	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MF185729	Mycobacterium phage KADY, complete genome	4359-4385	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN096368	Mycobacterium phage Soshari, complete genome	4358-4384	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT897907	Mycobacterium phage Grif, complete genome	4358-4384	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_004682	Mycobacterium virus Bxz2, complete genome	4369-4395	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK310140	Mycobacterium phage Gemma, complete genome	4310-4336	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH155864	Mycobacterium phage Beauxregard13, complete genome	4275-4301	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KY965063	Mycobacterium phage PurpleHaze, complete genome	4309-4335	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MT657331	Mycobacterium phage Manu, complete genome	4310-4336	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX670788	Mycobacterium phage Louie6, complete genome	4359-4385	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MK494128	Mycobacterium phage Heliosoles, complete genome	4310-4336	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN585984	Mycobacterium phage AgronaGT15, complete genome	4183-4209	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN284900	Mycobacterium phage JeppNRM, complete genome	4308-4334	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH450128	Mycobacterium phage Reba, complete genome	3981-4007	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_031074	Gordonia phage Bantam, complete genome	56566-56592	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH513975	Mycobacterium phage Misomonster, complete genome	4358-4384	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH450124	Mycobacterium phage Marius, complete genome	4310-4336	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH399776	Mycobacterium phage Grum1, complete genome	4268-4294	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KX458237	Mycobacterium phage Penny1, complete genome	4275-4301	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KP017310	Mycobacterium phage Phoxy, complete genome	4359-4385	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_021535	Mycobacterium phage Jobu08, complete genome	4338-4364	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH450126	Mycobacterium phage PhishRPhriends, complete genome	3501-3527	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH450119	Mycobacterium phage Kalnoky, complete genome	4310-4336	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MN062718	Mycobacterium phage SoilDragon, complete genome	3948-3974	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	MH371121	Mycobacterium phage Phranny, complete genome	4308-4334	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KP017311	Mycobacterium phage Spike509, complete genome	4359-4385	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	KF279418	Mycobacterium phage Anubis, complete genome	4143-4169	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP026091	Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence	693384-693410	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_LR134460	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 18, complete sequence	89948-89974	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_016138	Pseudomonas aeruginosa plasmid pUM505, complete sequence	31681-31707	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP012944	Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence	349119-349145	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NZ_CP039965	Pseudorhodobacter sp. S12M18 plasmid unnamed1, complete sequence	1363965-1363991	6	0.778
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_017575	Ralstonia solanacearum Po82 megaplasmid, complete sequence	693235-693261	6	0.778
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN693998	Marine virus AFVG_250M48, complete genome	15165-15194	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN693998	Marine virus AFVG_250M48, complete genome	14943-14972	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_021289	Burkholderia insecticola plasmid p1, complete sequence	1265952-1265981	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	1665262-1665291	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP018821	Sphingomonas koreensis strain ABOJV plasmid tig00000001, complete sequence	270826-270855	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP035511	Haematobacter massiliensis strain OT1 plasmid pOT1-1, complete sequence	22628-22657	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP016620	Microvirga ossetica strain V5/3m plasmid unnamed4, complete sequence	185367-185396	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_003324	Sinorhizobium phage PBC5, complete genome	56614-56643	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	AF448724	Sinorhizobium meliloti phage PBC5, complete genome	56614-56643	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_007353	Sphingomonas sp. A1 plasmid pA1 DNA, complete sequence	40830-40859	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	781-810	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1997297-1997326	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP054621	Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence	5859-5888	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_KY399978	Vibrio cholerae O139 strain ICDC-211 plasmid pVC211, complete sequence	39428-39457	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	1767634-1767663	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	1792653-1792682	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022766	Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence	1825104-1825133	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1853029-1853058	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP016555	Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence	1478673-1478702	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_020275	Mycobacterium intracellulare subsp. yongonense 05-1390 plasmid pMyong1, complete sequence	68034-68063	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052069	Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence	1757878-1757907	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	367291-367320	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP016905	Ralstonia solanacearum strain KACC 10709 plasmid unnamed1	730944-730973	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022769	Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence	1834588-1834617	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022773	Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence	1543354-1543383	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	1774918-1774947	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022791	Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence	1772734-1772763	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	1769788-1769817	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052071	Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence	1841775-1841804	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	1711119-1711148	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	1771153-1771182	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022779	Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence	1846068-1846097	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052075	Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence	1841742-1841771	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	1748004-1748033	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	1825503-1825532	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052105	Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence	1840485-1840514	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	CP054934	Nocardiopsis flavescens strain NA01583 plasmid unnamed1, complete sequence	130092-130121	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	1738229-1738258	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	1748316-1748345	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	1825503-1825532	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052115	Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence	1840584-1840613	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	1748004-1748033	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	1738876-1738905	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	1747207-1747236	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	1825503-1825532	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	1825503-1825532	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	1825503-1825532	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052107	Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence	1840580-1840609	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP013125	Pseudomonas mendocina S5.2 plasmid pPME5, complete sequence	172038-172067	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022781	Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence	1897919-1897948	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052117	Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence	1840569-1840598	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	1738252-1738281	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022793	Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence	1751296-1751325	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022785	Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence	1731935-1731964	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022787	Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence	1791831-1791860	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022756	Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence	1823819-1823848	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	1822818-1822847	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052121	Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence	1840569-1840598	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	1738252-1738281	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	1748315-1748344	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	CP011998	Ralstonia solanacearum strain YC45 plasmid, complete sequence	1761405-1761434	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP045548	Streptomyces sp. SYP-A7193 plasmid unnamed1, complete sequence	38550-38579	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052073	Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence	1841566-1841595	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	1738252-1738281	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	1738252-1738281	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052109	Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence	1840580-1840609	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	1825508-1825537	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052103	Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence	1840591-1840620	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052119	Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence	1840392-1840421	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP016613	Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence	873037-873066	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	294814-294843	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	879196-879225	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	67199-67228	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	660672-660701	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	540049-540078	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	638640-638669	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP022482	Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence	1330858-1330887	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP023068	Ensifer sojae CCBAU 05684 plasmid pSJ05684b, complete sequence	1669854-1669883	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	177001-177030	7	0.767
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	177001-177030	7	0.767
NZ_CP036292_22	22.3\|5447719\|27\|NZ_CP036292\|CRT	5447719-5447745	27	NC_012523	Rhodococcus opacus B4 plasmid pKNR, complete sequence	54154-54180	7	0.741
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_AP022611	Mycolicibacterium madagascariense strain JCM 13574 plasmid pJCM13574	204036-204065	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	466287-466316	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	LN997843	Streptomyces reticuli genome assembly TUE45, plasmid : II	441854-441883	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_041927	Sphingobium phage Lacusarx, complete genome	106735-106764	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP029830	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence	841119-841148	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN694595	Marine virus AFVG_250M567, complete genome	57967-57996	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR594669	Variovorax sp. SRS16 plasmid 4	291807-291836	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_009427	Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence	386629-386658	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP020441	Paracoccus yeei strain FDAARGOS_252 plasmid unnamed1, complete sequence	132713-132742	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	647830-647859	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP011665	Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence	322411-322440	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP044080	Paracoccus yeei strain FDAARGOS_643 plasmid unnamed3, complete sequence	119203-119232	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP031079	Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence	120672-120701	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR594673	Variovorax sp. PBL-E5 plasmid 3	271644-271673	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_016586	Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence	264264-264293	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP024423	Paracoccus yeei strain TT13 plasmid pTT13-1, complete sequence	71077-71106	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP007796	Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence	454112-454141	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1165705-1165734	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	4568813-4568842	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP040819	Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence	199340-199369	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_013852	Allochromatium vinosum DSM 180 plasmid pALVIN01, complete sequence	59040-59069	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP025547	Mycobacterium paragordonae strain 49061 plasmid unnamed1, complete sequence	98314-98343	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	23653-23682	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_009620	Sinorhizobium medicae WSM419 plasmid pSMED01, complete sequence	1123064-1123093	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_014007	Sphingobium japonicum UT26S plasmid pCHQ1, complete sequence	88976-89005	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MG872834	Gordonia phage Confidence, complete genome	15308-15337	8	0.733
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN693998	Marine virus AFVG_250M48, complete genome	15467-15496	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_010510	Methylobacterium radiotolerans JCM 2831 plasmid pMRAD01, complete sequence	256409-256438	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP029357	Azospirillum sp. CFH 70021 plasmid unnamed2	190915-190944	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_017958	Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence	261889-261918	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	CP000662	Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA01, complete sequence	613955-613984	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR594669	Variovorax sp. SRS16 plasmid 4	92642-92671	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP011518	Pandoraea oxalativorans strain DSM 23570 plasmid pPO70-1, complete sequence	29162-29191	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	CP000663	Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence	110667-110696	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP021819	Sinorhizobium meliloti strain M162 plasmid psymA, complete sequence	65237-65266	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP031752	Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence	56805-56834	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR594673	Variovorax sp. PBL-E5 plasmid 3	90955-90984	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	CP000385	Mycobacterium sp. MCS Plasmid1, complete sequence	121053-121082	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_008704	Mycobacterium sp. KMS plasmid pMKMS02, complete sequence	147112-147141	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP021082	Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence	252600-252629	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP039892	Agrobacterium tumefaciens strain CFBP5499 plasmid pAtCFBP5499c, complete sequence	58999-59028	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK820641	Gordonia phage EnalisNailo, complete genome	15463-15492	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK284520	Gordonia phage Lilas, complete genome	15463-15492	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN062715	Gordonia phage Marteena, complete genome	15314-15343	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK433275	Gordonia phage EMsquaredA, complete genome	15314-15343	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	KC661275	Mycobacterium phage HINdeR, complete genome	4967-4996	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MK433274	Gordonia phage Bradissa, complete genome	15461-15490	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MH513979	Gordonia phage Pollux, complete genome	15314-15343	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MT521999	Gordonia Phage Jablanski, complete genome	15413-15442	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_030942	Gordonia phage BritBrat, complete genome	15314-15343	9	0.7
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	KC117377	Halovirus HVTV-1, complete genome	63970-63999	9	0.7
NZ_CP036292_12	12.1\|2859742\|33\|NZ_CP036292\|CRISPRCasFinder	2859742-2859774	33	NZ_CP015231	Epibacterium mobile F1926 plasmid unnamed1, complete sequence	271948-271980	10	0.697
NZ_CP036292_12	12.1\|2859742\|33\|NZ_CP036292\|CRISPRCasFinder	2859742-2859774	33	NZ_CP015231	Epibacterium mobile F1926 plasmid unnamed1, complete sequence	474022-474054	10	0.697
NZ_CP036292_12	12.1\|2859742\|33\|NZ_CP036292\|CRISPRCasFinder	2859742-2859774	33	NZ_CP015231	Epibacterium mobile F1926 plasmid unnamed1, complete sequence	928178-928210	10	0.697
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	217874-217903	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR594669	Variovorax sp. SRS16 plasmid 4	298200-298229	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1819165-1819194	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP029211	Aquabacterium olei strain NBRC 110486 plasmid pTB101, complete sequence	47579-47608	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_LR594673	Variovorax sp. PBL-E5 plasmid 3	278041-278070	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	1808140-1808169	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NZ_CP024895	Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence	73104-73133	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	NC_013859	Azospirillum sp. B510 plasmid pAB510e, complete sequence	227856-227885	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	KT870145	Roseobacter phage DSS3P8, complete genome	44885-44914	10	0.667
NZ_CP036292_22	22.2\|5447671\|30\|NZ_CP036292\|CRT	5447671-5447700	30	MN602268	Bacteriophage DSS3_MAL1, complete genome	44659-44688	10	0.667

1. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP015073 (Escherichia coli strain Ecol_743 plasmid pEC743_4, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

2. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_KM670336 (Salmonella enterica subsp. enterica serovar Senftenberg strain SRC119 plasmid pSRC119-A/C, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

3. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP045255 (Proteus mirabilis strain L90-1 plasmid pL902, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

4. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN543575 (Klebsiella pneumoniae strain GH44TC plasmid pGH44TC_fusion, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

5. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to AP018710 (Uncultured bacterium plasmid pSN1216-29 DNA, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

6. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP047338 (Klebsiella pneumoniae strain 2019036D plasmid p2019036D-50kb, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

7. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP020602 (Pseudomonas aeruginosa strain E6130952 plasmid pJHX613, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

8. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_MK262712 (Klebsiella pneumoniae strain KP18-29 plasmid p18-29-MDR, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

9. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_MF174859 (Escherichia coli strain 6/14/6b plasmid pIncHI2-MU3, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

10. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP014764 (Klebsiella pneumoniae strain KPNIH39 plasmid pKPN-704, complete sequence) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

11. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR745047 (Klebsiella pneumoniae isolate Kpn2166 plasmid pCTX-M15_Kpn2166) position: , mismatch: 3, identity: 0.9

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---gccgcccatacctgc	Protospacer
***************   ************

12. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT740732 (Ralstonia phage Darius, complete genome) position: , mismatch: 3, identity: 0.889

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ccccatggcgccagcgaagccgccgcc	Protospacer
 ****** ***** *************

13. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT361768 (Ralstonia phage RPZH6, complete genome) position: , mismatch: 3, identity: 0.889

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ccccatggcgccagcgaagccgccgcc	Protospacer
 ****** ***** *************

14. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT740740 (Ralstonia phage Gervaise, complete genome) position: , mismatch: 3, identity: 0.889

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ccccatggcgccagcgaagccgccgcc	Protospacer
 ****** ***** *************

15. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP029835 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed5, complete sequence) position: , mismatch: 3, identity: 0.889

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccaggccgccatcgaagccgccgtc	Protospacer
***** *******.***********.*

16. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP019083 (Paludisphaera borealis strain PX4 plasmid PALBO1, complete sequence) position: , mismatch: 3, identity: 0.889

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gaccatgccgccgccgaagccgccgtc	Protospacer
* **********.************.*

17. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP010410 (Xanthomonas sacchari strain R1 plasmid unnamed, complete sequence) position: , mismatch: 3, identity: 0.889

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gaccacgccgccaccgtagccgccgcc	Protospacer
* ***.********** **********

18. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN693998 (Marine virus AFVG_250M48, complete genome) position: , mismatch: 4, identity: 0.867

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
accaccgccgcccatgccgccgcccatgcc	Protospacer
  .************************.**

19. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_016588 (Azospirillum lipoferum 4B plasmid AZO_p6, complete sequence) position: , mismatch: 4, identity: 0.867

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
caggccgccgcccaggccgccgcccagacc	Protospacer
** .********** *********** ***

20. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_021289 (Burkholderia insecticola plasmid p1, complete sequence) position: , mismatch: 4, identity: 0.867

catacc---gccgcccatgccgccgcccatacc	CRISPR spacer
---acccatgccgcccatgccgccgcccatccc	Protospacer
   ***   ********************* **

21. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LN832562 (Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence) position: , mismatch: 4, identity: 0.867

cataccg-ccgcccatgccgccgcccatacc	CRISPR spacer
-atgccgcccgcccttgccgccgcccatatc	Protospacer
 **.*** ****** **************.*

22. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcgcccgccgccaccgaagccgccgac	Protospacer
** * .******************* *

23. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH590593 (Mycobacterium phage Rabinovish, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

24. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX781992 (Mycobacterium phage Gabriel, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

25. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH697579 (Mycobacterium phage Cane17, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

26. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112554 (Mycobacterium phage TinyTim, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

27. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359314 (Mycobacterium phage Ewok, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

28. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359337 (Mycobacterium phage Flabslab, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

29. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN234193 (Mycobacterium phage Kboogie, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

30. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450432 (Mycobacterium phage ValleyTerrace, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

31. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH051261 (Mycobacterium phage Tyke, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

32. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH779502 (Mycobacterium phage FudgeTart, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

33. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359365 (Mycobacterium phage Loanshark, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

34. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359311 (Mycobacterium phage SmallFry, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

35. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359364 (Mycobacterium phage ChickenPhender, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

36. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359303 (Mycobacterium phage Shnickers, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

37. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH697586 (Mycobacterium phage InigoMontoya, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

38. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112549 (Mycobacterium phage Morizzled23, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

39. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112541 (Mycobacterium phage Jessibeth14, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

40. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359347 (Mycobacterium phage Ading, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

41. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450425 (Mycobacterium phage Shelob, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

42. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_023714 (Mycobacterium phage LinStu, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

43. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359358 (Mycobacterium phage Essence, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

44. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KJ595575 (Mycobacterium phage Willis, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

45. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MG812493 (Mycobacterium phage NuevoMundo, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

46. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359339 (Mycobacterium phage Naija, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

47. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359333 (Mycobacterium phage JustHall, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

48. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KT321476 (Mycobacterium phage Zeenon, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

49. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN428065 (Mycobacterium phage Cactojaque, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

50. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359306 (Mycobacterium phage Norm, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

51. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN735434 (Mycobacterium phage Mangeria, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

52. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JN699625 (Mycobacterium phage Wally, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

53. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to EU826471 (Mycobacterium phage Cali, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

54. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX721255 (Mycobacterium phage Yucca, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

55. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359366 (Mycobacterium phage Basquiat, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

56. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359346 (Mycobacterium phage NoodleTree, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

57. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JN699013 (Mycobacterium phage Pio, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

58. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359361 (Mycobacterium phage Darko, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

59. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_023725 (Mycobacterium phage Nappy, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

60. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359348 (Mycobacterium phage Rahel, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

61. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH779498 (Mycobacterium phage Bread, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

62. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450427 (Mycobacterium phage Adlitam, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

63. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MG812494 (Mycobacterium phage Pier, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

64. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to GQ303262 (Mycobacterium phage LRRHood, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

65. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT818423 (Mycobacterium phage Janiyra, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

66. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH316567 (Mycobacterium phage ParkTD, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

67. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to AY129337 (Mycobacteriophage Bxz1, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

68. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH051260 (Mycobacterium phage InterFolia, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

69. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX721256 (Mycobacterium phage Erdmann, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

70. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359328 (Mycobacterium phage EmmaElysia, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

71. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KM881426 (Mycobacterium phage ZygoTaiga) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

72. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359335 (Mycobacterium phage Patter, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

73. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT889395 (Mycobacterium phage Shifa, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

74. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to EU826467 (Mycobacterium phage Rizal, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

75. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT723944 (Mycobacterium phage ChaylaJr, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

76. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KR080196 (Mycobacterium phage Momo, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

77. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH910040 (Mycobacterium phage Sauce, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

78. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF919495 (Mycobacterium phage Bigswole, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

79. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359318 (Mycobacterium phage Specks, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

80. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KF024734 (Mycobacterium phage Shrimp, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

81. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112548 (Mycobacterium phage McWolfish, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

82. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359308 (Mycobacterium phage Shaqnato, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

83. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112545 (Mycobacterium phage Khaleesi, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

84. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH825697 (Mycobacterium phage Bangla1971, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

85. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359338 (Mycobacterium phage Amataga, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

86. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359350 (Mycobacterium phage Nidhogg, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

87. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT723945 (Mycobacterium phage Quasimodo, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

88. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359342 (Mycobacterium phage ShiaLabeouf, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

89. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH316561 (Mycobacterium phage Derek, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

90. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112533 (Mycobacterium phage Bonray, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

91. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450422 (Mycobacterium phage RoMag, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

92. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359327 (Mycobacterium phage EmToTheThree, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

93. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH727543 (Mycobacterium phage CharlieB, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

94. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JF704116 (Mycobacterium phage Drazdys, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

95. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359336 (Mycobacterium phage Chargie21, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

96. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359355 (Mycobacterium phage Sprinklers, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

97. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112534 (Mycobacterium phage Burrough, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

98. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF919499 (Mycobacterium phage Daffodil, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

99. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359334 (Mycobacterium phage Delilah, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

100. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_023696 (Mycobacterium phage Dandelion, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

101. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN276192 (Mycobacterium phage Trinitium, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

102. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359324 (Mycobacterium phage Tortoise16, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

103. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH825713 (Mycobacterium phage Zalkecks, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

104. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359349 (Mycobacterium phage FoxtrotP1, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

105. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JF704096 (Mycobacterium phage Ghost, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

106. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN062707 (Mycobacterium phage Grungle, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

107. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359344 (Mycobacterium phage Napoleon13, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

108. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH727558 (Mycobacterium phage Salacia, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

109. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359363 (Mycobacterium phage Fludd, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

110. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX831080 (Mycobacterium phage Lukilu, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

111. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359329 (Mycobacterium phage Kamryn, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

112. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JQ911768 (Mycobacterium phage Ava3, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

113. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_004687 (Mycobacterium phage Bxz1, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

114. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_011270 (Mycobacterium phage Spud, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

115. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN183280 (Mycobacteriophage LolaVinca, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

116. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359345 (Mycobacterium phage QBert, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

117. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to GQ303260 (Mycobacterium phage ET08, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

118. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH744422 (Mycobacterium phage Roots515, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

119. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359321 (Mycobacterium phage Phusco, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

120. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359362 (Mycobacterium phage Atlantean, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

121. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to EU826469 (Mycobacterium phage ScottMcG, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

122. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK310143 (Mycobacterium phage Dietrick, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

123. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450429 (Mycobacterium phage Bipolarisk, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

124. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH051266 (Mycobacterium phage MikeLiesIn, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

125. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_029044 (Mycobacterium phage Breeniome, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

126. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK494105 (Mycobacterium phage Pinnie, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccttgccgccaccgacgccgccgtt	Protospacer
**** ************ *******..

127. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH669008 (Mycobacterium phage Megamind, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

128. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK878897 (Mycobacterium phage Blackbrain, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

129. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450434 (Mycobacterium phage DrPhinkDaddy, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

130. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359359 (Mycobacterium phage Colt, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

131. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF919527 (Mycobacterium phage Phox, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

132. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT818416 (Mycobacterium phage BackyardAgain, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

133. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359330 (Mycobacterium phage Iota, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

134. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KT365398 (Mycobacterium phage DTDevon, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

135. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX369583 (Mycobacterium phage Littleton, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

136. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF919494 (Mycobacterium phage BeanWater, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

137. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_028869 (Mycobacterium phage HyRo, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

138. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KT365400 (Mycobacterium phage ErnieJ, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

139. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KC691257 (Mycobacterium phage Astraea, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

140. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MG872839 (Mycobacterium phage LifeSavor, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

141. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KC748968 (Mycobacterium phage Gizmo, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

142. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KC748970 (Mycobacterium phage ArcherS7, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

143. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359353 (Mycobacterium phage BadAgartude, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

144. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH697590 (Mycobacterium phage Phlegm, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

145. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359317 (Mycobacterium phage FrayBell, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

146. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT553335 (Mycobacterium phage Ronan, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

147. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN428066 (Mycobacterium phage JPickles, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

148. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359305 (Mycobacterium phage Teardrop, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

149. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to DQ398053 (Mycobacteriophage Catera, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

150. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF919513 (Mycobacterium phage Koguma, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

151. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JN699626 (Mycobacterium phage MoMoMixon, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

152. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_028986 (Mycobacterium phage Alice, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

153. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450424 (Mycobacterium phage Melpomini, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

154. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JN204348 (Mycobacterium phage Sebata, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

155. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN183285 (Mycobacterium phage YoungMoneyMata, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

156. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK450423 (Mycobacterium phage Stubby, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

157. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF919493 (Mycobacterium phage Audrick, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

158. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_008207 (Mycobacterium phage Catera, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

159. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JN624850 (Mycobacterium phage Pleione, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

160. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK359326 (Mycobacterium phage Pivoine, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccaccgacgccaccgat	Protospacer
***************** ***.*** .

161. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP023066 (Sinorhizobium sp. CCBAU 05631 plasmid pSS05631d, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtacatgccgccaccgacgtcgccgcc	Protospacer
*. ************** *.*******

162. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP025114 (Bradyrhizobium sp. SK17 strain CBNU plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
tcccatgccgcccccgaacccgccggc	Protospacer
 *********** ***** ****** *

163. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP025114 (Bradyrhizobium sp. SK17 strain CBNU plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
tcccatgccgcccccgaacccgccggc	Protospacer
 *********** ***** ****** *

164. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP021126 (Rhizobium sp. Kim5 plasmid pRetKim5b, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ggccatgccgcgatcgaagccgccgcg	Protospacer
* ********* *.************

165. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP013516 (Rhizobium sp. N1314 plasmid pRspN1314e, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gaacatgccggcaccgatgccgccgcc	Protospacer
*  ******* ****** *********

166. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP054029 (Rhizobium sp. JKLM19E plasmid pPR19E02, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gaacatgccggcaccgatgccgccgcc	Protospacer
*  ******* ****** *********

167. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcgctggccgccgccgaagccgccgcc	Protospacer
** *  ******.**************

168. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccgcggccgccaccgaaaccgccgcc	Protospacer
***   ************.********

169. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP015231 (Epibacterium mobile F1926 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccagcgccgccaccaaagccgccgcc	Protospacer
*** ..*********.***********

170. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP054613 (Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcctccgccaccaccgaagccgccgcc	Protospacer
***. .***.*****************

171. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH697583 (Mycobacterium phage EricMillard, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

172. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH727551 (Mycobacterium phage Kalah2, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

173. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF919504 (Mycobacterium phage DmpstrDiver, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

174. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH669017 (Mycobacterium phage Zelink, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

175. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN062701 (Mycobacterium phage Dallas, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

176. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK524527 (Mycobacterium phage ThreeRngTarjay, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

177. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK524529 (Mycobacterium phage Phoebus, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

178. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK524504 (Mycobacterium phage Hughesyang, complete genome) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccaccgccgccactgaagccgccgcc	Protospacer
***  .********.************

179. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP013104 (Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcacgcgccgccaccgatgccgccgcc	Protospacer
** *..*********** *********

180. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_LR134456 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence) position: , mismatch: 4, identity: 0.852

---gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ctggcc---gccgccaccgaaaccgccgcc	Protospacer
   ***   ************.********

181. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gccgcggccgccaccgaaaccgccgcc	Protospacer
***   ************.********

182. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcacgcgccgccaccgatgccgccgcc	Protospacer
** *..*********** *********

183. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP014769 (Hymenobacter sp. PAMC 26554 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaag-ccgccgcc	CRISPR spacer
gcccaggccgccaccgaagcccagcgc-	Protospacer
***** ************* **. ***

184. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP025432 (Paracoccus zhejiangensis strain J6 plasmid pPZ02, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcgctcgccgcccccgaagccgccgcc	Protospacer
** * .****** **************

185. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP017563 (Paraburkholderia sprentiae WSM5005 plasmid pl1WSM5005, complete sequence) position: , mismatch: 4, identity: 0.852

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcgcgcgccgccaccgacgccgccgcc	Protospacer
** *..*********** *********

186. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP029357 (Azospirillum sp. CFH 70021 plasmid unnamed2) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggtgccgccgcccatgccgccgcccatgac	Protospacer
 .*.***********************. *

187. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR134456 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 14, complete sequence) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gagcgcgccgcccatgccgccgcccatgcc	Protospacer
 *   **********************.**

188. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 5, identity: 0.833

--cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccttgc--ccgcccatgccgccgcccagacc	Protospacer
  * *.*  ******************* ***

189. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP016619 (Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcc---catacc	CRISPR spacer
cataccaccacccatgccgccgccaggcat---	Protospacer
******.**.**************   ***

190. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP016620 (Microvirga ossetica strain V5/3m plasmid unnamed4, complete sequence) position: , mismatch: 5, identity: 0.833

---cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gtccat---gccacccatgccgccgcccatgcc	Protospacer
   ***   ***.*****************.**

191. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK279905 (Mycobacterium phage Acquire49, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

192. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MF185726 (Mycobacterium phage Appletree2, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

193. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK310144 (Mycobacterium phage CicholasNage, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

194. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MH744425 (Mycobacterium phage Wamburgrxpress, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

195. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to JN600672 (Mycobacterium phage Fezzik, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

196. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN586018 (Mycobacterium phage Wyatt2, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

197. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN096382 (Mycobacterium phage AvadaKedavra, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

198. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK494100 (Mycobacterium phage Halena, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

199. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to JF704113 (Mycobacterium phage UPIE, complete sequence) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

200. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_042313 (Mycobacterium virus JoeDirt, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

201. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to HM152763 (Mycobacterium virus Bron, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

202. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN586023 (Mycobacterium phage Zaria, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

203. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MT771349 (Mycobacterium phage Tyson, complete genome) position: , mismatch: 5, identity: 0.833

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cttaccgccgcccttgccgccgccagaacc	Protospacer
* *********** ********** . ***

204. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP026093 (Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atggatgccaccaccgaagccgccgcc	Protospacer
..  *****.*****************

205. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP011053 (Halomonas sp. KO116 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
agcgccgccgccaccgaagccgccgcc	Protospacer
. *  .*********************

206. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN693998 (Marine virus AFVG_250M48, complete genome) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
accaccgccgccaccgaagccgccacc	Protospacer
.**  .******************.**

207. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP017244 (Rhizobium etli 8C-3 plasmid pRsp8C3c, complete sequence) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
tatcatgcagccaccgcagccgccgcc	Protospacer
  .***** ******* **********

208. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
accgccgccgccaccgaagccgccgcg	Protospacer
.**  .********************

209. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP017105 (Rhizobium gallicum strain IE4872 plasmid pRgalIE4872d, complete sequence) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
tatcatgcagccaccgcagccgccgcc	Protospacer
  .***** ******* **********

210. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to CP006880 (Rhizobium gallicum bv. gallicum R602 plasmid pRgalR602c, complete sequence) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
tatcatgcagccaccgcagccgccgcc	Protospacer
  .***** ******* **********

211. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT310895 (Arthrobacter phage StevieBAY, complete genome) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtagttgccgccgccgaagccgccgcc	Protospacer
*.   *******.**************

212. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP048636 (Rhizobium oryzihabitans strain M15 plasmid p4, complete sequence) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgacaccaccgaagccgcgcca	Protospacer
******* *.*************  *

213. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK284518 (Mycobacterium phage ACFishhook, complete genome) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtcgccgccgtcaccgaagccgccgcc	Protospacer
*.*  .****.****************

214. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK279903 (Mycobacterium phage Zetzy, complete genome) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtcactgccgtcaccgaagccgccgcg	Protospacer
*.*  *****.***************

215. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_031074 (Gordonia phage Bantam, complete genome) position: , mismatch: 5, identity: 0.815

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtcggagccgccgccgaagccgccgcc	Protospacer
*.* . ******.**************

216. spacer 17.1|4360235|29|NZ_CP036292|CRISPRCasFinder matches to NC_020894 (Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence) position: , mismatch: 6, identity: 0.793

accgcaagctggctcgaagccacatgctg-	CRISPR spacer
cccgcaagctggttcgaaggcaca-acggc	Protospacer
 ***********.****** **** .* *

217. spacer 17.1|4360235|29|NZ_CP036292|CRISPRCasFinder matches to NC_017766 (Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence) position: , mismatch: 6, identity: 0.793

accgcaagctggctcgaagccacatgctg-	CRISPR spacer
cccgcaagctggttcgaaggcaca-acggc	Protospacer
 ***********.****** **** .* *

218. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_016626 (Burkholderia sp. YI23 plasmid byi_1p, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
caactcgccgcccatgccgccgcccaccgc	Protospacer
**  .*********************.  *

219. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP024310 (Sinorhizobium fredii strain NXT3 plasmid pSfreNXT3c, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gataccgacgcccttgccgccgccctcgcc	Protospacer
 ****** ***** *********** ..**

220. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP023064 (Sinorhizobium sp. CCBAU 05631 plasmid pSS05631b, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gataccgacgcccttgccgccgccctcgcc	Protospacer
 ****** ***** *********** ..**

221. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cggatcgccgcctatgccgccgcccatcca	Protospacer
*. *.*******.************** *

222. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 6, identity: 0.8

--cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccttgc--ccgcccaggccgccgcccagacc	Protospacer
  * *.*  ******* *********** ***

223. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP005085 (Sphingobium sp. TKS plasmid pTK1, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gatatcgccgccgatgccgccgccggcacc	Protospacer
 ***.******* *********** ..***

224. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.8

--cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccttgc--ccgcccaggccgccgcccagacc	Protospacer
  * *.*  ******* *********** ***

225. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP038257 (Microbacterium sediminis strain YLB-01 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
aacaccgtcgcccaggccgccgcccaggcc	Protospacer
 *.****.****** *********** .**

226. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to KU958700 (Streptomyces phage Chymera, complete genome) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tacaccgccgccgaggccgccgcccaagcc	Protospacer
.*.********* * *********** .**

227. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP020911 (Rhizobium etli strain NXC12 plasmid pRetNXC12e, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
caggccgccgccgatcccgccgcccatgcg	Protospacer
** .******** ** ***********.*

228. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_021911 (Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1f, complete sequence) position: , mismatch: 6, identity: 0.8

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
caggccgccgccgatcccgccgcccatgcg	Protospacer
** .******** ** ***********.*

229. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK637516 (Agrobacterium phage Milano, complete genome) position: , mismatch: 6, identity: 0.8

cataccgccgcccatg---ccgccgcccatacc	CRISPR spacer
gccaccgccgcccatgccaccgccgcccat---	Protospacer
  .*************   ***********

230. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP030841 (Acidisarcina polymorpha strain SBC82 plasmid pACPOL1, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gcccatgccgccgccgaagccgagaaa	Protospacer
************.*********  .

231. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF377441 (Arthrobacter phage Timinator, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ctggttgccgccgccgaagccgccgcc	Protospacer
 .   *******.**************

232. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KU647629 (Arthrobacter phage BarretLemon, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ctggttgccgccgccgaagccgccgcc	Protospacer
 .   *******.**************

233. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN693999 (Marine virus AFVG_250M363, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ggaaccgccgccaccgaagccgccacc	Protospacer
*    .******************.**

234. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_049468 (Arthrobacter phage Zartrosa, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ctggttgccgccgccgaagccgccgcc	Protospacer
 .   *******.**************

235. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atggatgccaccaccgaggccgccgcc	Protospacer
..  *****.*******.*********

236. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_009717 (Xanthobacter autotrophicus Py2 plasmid pXAUT01, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
acccatgccgccacccatgccgccctg	Protospacer
.************** * ****** .

237. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP012940 (Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atggatgccaccaccgaggccgccgcc	Protospacer
..  *****.*******.*********

238. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP031599 (Roseovarius indicus strain DSM 26383 plasmid pRIdsm_01, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
cccgatgccgccaccgaacccgccata	Protospacer
 ** ************** *****..

239. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP043477 (Xanthomonas hyacinthi strain CFBP 1156 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
cgctgcgccggcaccgaagccgccgcc	Protospacer
  *...**** ****************

240. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP021373 (Rhizobium sp. ACO-34A plasmid pRACO34Ac, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atccatgccgccgccgaagccgctcgc	Protospacer
..**********.**********.  *

241. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_017966 (Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ccccgtaccgccaccgaagccgccctt	Protospacer
 ***.*.***************** ..

242. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
ctgaacgccgccatcgaagccgccgcc	Protospacer
 .  *.*******.*************

243. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP051295 (Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atggatgccaccaccgaggccgccgcc	Protospacer
..  *****.*******.*********

244. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_019202 (Pseudomonas aeruginosa plasmid pKLC102, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gatatcgccgccaccgaagccgcagcc	Protospacer
* .  .***************** ***

245. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP025188 (Roseomonas mucosa strain AD2 plasmid p1-AD2, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
acccctaccgccaccgaagccgccttt	Protospacer
.*** *.***************** ..

246. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP032156 (Mycobacterium sp. ELW1 plasmid pELW1-1, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gagatcgccgtcaccgaagccgccgcc	Protospacer
*    .****.****************

247. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MG925355 (Mycobacterium phage OlanP, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

248. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK112543 (Mycobacterium Phage Kalb97, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

249. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK967399 (Mycobacterium phage Groupthink, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

250. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX523125 (Mycobacterium phage BuzzBuzz, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

251. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KC661272 (Mycobacterium phage Methuselah, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

252. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MG925341 (Mycobacteriophage EpicPhail, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

253. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to JF704114 (Mycobacterium phage Vix, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

254. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK279913 (Mycobacterium phage PotatoSplit, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

255. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MF185729 (Mycobacterium phage KADY, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

256. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN096368 (Mycobacterium phage Soshari, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

257. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT897907 (Mycobacterium phage Grif, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

258. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_004682 (Mycobacterium virus Bxz2, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

259. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK310140 (Mycobacterium phage Gemma, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

260. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH155864 (Mycobacterium phage Beauxregard13, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

261. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KY965063 (Mycobacterium phage PurpleHaze, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

262. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MT657331 (Mycobacterium phage Manu, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

263. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX670788 (Mycobacterium phage Louie6, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

264. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MK494128 (Mycobacterium phage Heliosoles, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

265. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN585984 (Mycobacterium phage AgronaGT15, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

266. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN284900 (Mycobacterium phage JeppNRM, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

267. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH450128 (Mycobacterium phage Reba, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

268. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_031074 (Gordonia phage Bantam, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gaagccgccgccaccgaacccgccgcc	Protospacer
*    .************ ********

269. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH513975 (Mycobacterium phage Misomonster, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

270. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH450124 (Mycobacterium phage Marius, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

271. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH399776 (Mycobacterium phage Grum1, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

272. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KX458237 (Mycobacterium phage Penny1, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

273. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KP017310 (Mycobacterium phage Phoxy, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

274. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_021535 (Mycobacterium phage Jobu08, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

275. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH450126 (Mycobacterium phage PhishRPhriends, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

276. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH450119 (Mycobacterium phage Kalnoky, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

277. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MN062718 (Mycobacterium phage SoilDragon, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

278. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to MH371121 (Mycobacterium phage Phranny, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

279. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KP017311 (Mycobacterium phage Spike509, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

280. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to KF279418 (Mycobacterium phage Anubis, complete genome) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gtgaccgccgtcaccgaagccgccgcc	Protospacer
*.   .****.****************

281. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP026091 (Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atggatgccaccaccgaggccgccgcc	Protospacer
..  *****.*******.*********

282. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_LR134460 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 18, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gaatccgccgccgccgaagccgccgcc	Protospacer
*  . .******.**************

283. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_016138 (Pseudomonas aeruginosa plasmid pUM505, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
gatatcgccgccaccgaagccgcagcc	Protospacer
* .  .***************** ***

284. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP012944 (Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atggatgccaccaccgaggccgccgcc	Protospacer
..  *****.*******.*********

285. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NZ_CP039965 (Pseudorhodobacter sp. S12M18 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
agccatgccgccgccgaaaccgccgtg	Protospacer
. **********.*****.******.

286. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_017575 (Ralstonia solanacearum Po82 megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.778

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
atggatgccaccaccgaggccgccgcc	Protospacer
..  *****.*******.*********

287. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN693998 (Marine virus AFVG_250M48, complete genome) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
catgccgccgcccatgccgccgccgtctgg	Protospacer
***.********************  .

288. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN693998 (Marine virus AFVG_250M48, complete genome) position: , mismatch: 7, identity: 0.767

---cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gcccat---gccgcccatgccgccacccatggg	Protospacer
   ***   ***************.*****.

289. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_021289 (Burkholderia insecticola plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagcgccacgcccatgccgccgccgataca	Protospacer
**   *  **************** ****

290. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggtatcgccgcccatgccgccgcccggctc	Protospacer
 .**.********************.  .*

291. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP018821 (Sphingomonas koreensis strain ABOJV plasmid tig00000001, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cattccgccgcccatgccgccgctgaaggt	Protospacer
*** *******************. * . .

292. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP035511 (Haematobacter massiliensis strain OT1 plasmid pOT1-1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggcgccgccgtccatgccgccgccgatacg	Protospacer
 ...******.************* ****

293. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP016620 (Microvirga ossetica strain V5/3m plasmid unnamed4, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc-	CRISPR spacer
gagcccgccgcccatgccgccaccc-tgctg	Protospacer
 *  *****************.*** *.*.

294. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_003324 (Sinorhizobium phage PBC5, complete genome) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ttgcccgcgacccatgccgccgcccataac	Protospacer
.   **** .****************** *

295. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to AF448724 (Sinorhizobium meliloti phage PBC5, complete genome) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ttgcccgcgacccatgccgccgcccataac	Protospacer
.   **** .****************** *

296. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_007353 (Sphingomonas sp. A1 plasmid pA1 DNA, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc-	CRISPR spacer
ggcaccgccgcccatgccgccggcc-tgctg	Protospacer
 ..******************* ** *.*.

297. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gagcgcgccgccaatgccgccgcccatggc	Protospacer
 *   ******* **************. *

298. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

299. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP054621 (Azospirillum oryzae strain KACC 14407 plasmid unnamed6, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ctgcgccccggctatgccgccgcccatacc	Protospacer
*    * *** *.*****************

300. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_KY399978 (Vibrio cholerae O139 strain ICDC-211 plasmid pVC211, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cgtgccgccgcccatgccgccggccgagac	Protospacer
*.*.****************** **. . *

301. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

302. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

303. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022766 (Ralstonia solanacearum strain T78 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

304. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

305. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP016555 (Ralstonia solanacearum FJAT-1458 plasmid plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

306. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_020275 (Mycobacterium intracellulare subsp. yongonense 05-1390 plasmid pMyong1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc---	CRISPR spacer
cataccgccgcccat---cccgcctgcacccag	Protospacer
***************    *****...***

307. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052069 (Ralstonia solanacearum strain FJAT91.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

308. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

309. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP016905 (Ralstonia solanacearum strain KACC 10709 plasmid unnamed1) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

310. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022769 (Ralstonia solanacearum strain T60 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

311. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022773 (Ralstonia solanacearum strain T42 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

312. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

313. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022791 (Ralstonia solanacearum strain SL3103 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

314. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

315. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052071 (Ralstonia solanacearum strain FJAT454.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

316. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

317. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

318. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022779 (Ralstonia solanacearum strain SL3882 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

319. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052075 (Ralstonia solanacearum strain FJAT448.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

320. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

321. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

322. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052105 (Ralstonia solanacearum strain FJAT15252.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

323. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to CP054934 (Nocardiopsis flavescens strain NA01583 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc-	CRISPR spacer
gacaccgccgcccacgccgccg-ccacgctg	Protospacer
 *.***********.******* ***..*.

324. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

325. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

326. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

327. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052115 (Ralstonia solanacearum strain FJAT1463.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

328. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

329. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

330. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

331. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

332. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

333. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

334. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052107 (Ralstonia solanacearum strain FJAT15249.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

335. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP013125 (Pseudomonas mendocina S5.2 plasmid pPME5, complete sequence) position: , mismatch: 7, identity: 0.767

---cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gcgcat---gccgcccatgccgctgcccatggt	Protospacer
   ***   **************.******. .

336. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022781 (Ralstonia solanacearum strain SL3822 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

337. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052117 (Ralstonia solanacearum strain FJAT1463.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

338. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

339. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022793 (Ralstonia solanacearum strain SL2729 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

340. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022785 (Ralstonia solanacearum strain SL3730 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

341. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022787 (Ralstonia solanacearum strain SL3300 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

342. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022756 (Ralstonia solanacearum strain T117 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

343. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

344. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052121 (Ralstonia solanacearum strain FJAT1458.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

345. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

346. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

347. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to CP011998 (Ralstonia solanacearum strain YC45 plasmid, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

348. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP045548 (Streptomyces sp. SYP-A7193 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccaccgccgcccgtgccgccgccgaatcc	Protospacer
  .**********.********** *  **

349. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052073 (Ralstonia solanacearum strain FJAT448.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

350. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

351. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

352. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052109 (Ralstonia solanacearum strain FJAT15249.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

353. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

354. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052103 (Ralstonia solanacearum strain FJAT15252.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

355. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052119 (Ralstonia solanacearum strain FJAT1458.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

356. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP016613 (Ralstonia solanacearum FJAT-91 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

357. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

358. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

359. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

360. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

361. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

362. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

363. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP022482 (Ralstonia solanacearum strain HA4-1 plasmid HA4-1MP, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

364. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP023068 (Ensifer sojae CCBAU 05684 plasmid pSJ05684b, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gaggccgccgcccatgcccccggccatgcg	Protospacer
 * .************** *** ****.*

365. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

366. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cagatcgccgcccatgccgccgcgcgcggc	Protospacer
** *.****************** *... *

367. spacer 22.3|5447719|27|NZ_CP036292|CRT matches to NC_012523 (Rhodococcus opacus B4 plasmid pKNR, complete sequence) position: , mismatch: 7, identity: 0.741

gcccatgccgccaccgaagccgccgcc	CRISPR spacer
aagttggcggccaccgaagccgccgcc	Protospacer
.  .  ** ******************

368. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_AP022611 (Mycolicibacterium madagascariense strain JCM 13574 plasmid pJCM13574) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cgcgccgccgcccatgccgccgggcatggg	Protospacer
*...******************  ***.

369. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
acccgcgccgcccatgccgccgccgatgca	Protospacer
  .  ******************* **.*

370. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to LN997843 (Streptomyces reticuli genome assembly TUE45, plasmid : II) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gcgaccgccgcccaggccgccgccctggtc	Protospacer
   *********** **********  ..*

371. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_041927 (Sphingobium phage Lacusarx, complete genome) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggcacagccgcccatgccgccgccgatcag	Protospacer
 ..** ****************** **

372. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP029830 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tcgaccgccgcccatgtcgccgccgtcgcc	Protospacer
.  *************.*******  ..**

373. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN694595 (Marine virus AFVG_250M567, complete genome) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
aggatcgccgcccatgccaccgcccatgtg	Protospacer
 . *.*************.********..

374. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR594669 (Variovorax sp. SRS16 plasmid 4) position: , mismatch: 8, identity: 0.733

catacc---gccgcccatgccgccgcccatacc	CRISPR spacer
---atccgagccgcccttgccgccgcccatcgg	Protospacer
   *.*   ******* *************

375. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_009427 (Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tctaccgccgcctttgccgccgcccggcac	Protospacer
. **********. ***********.   *

376. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP020441 (Paracoccus yeei strain FDAARGOS_252 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tctgccgccgcccttgccgccgccccggcg	Protospacer
. *.********* ***********  .*

377. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
accaccgccgccccggccgccgcccagccg	Protospacer
  .**********  ***********  *

378. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP011665 (Streptomyces sp. Mg1 plasmid pSMg1-1, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gcccccgccgcccatgccggcgctcatcac	Protospacer
  . *************** ***.***  *

379. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP044080 (Paracoccus yeei strain FDAARGOS_643 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tctgccgccgcccttgccgccgccccggcg	Protospacer
. *.********* ***********  .*

380. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP031079 (Paracoccus yeei strain CCUG 32053 plasmid pYEE1, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tctgccgccgcccttgccgccgccccggcg	Protospacer
. *.********* ***********  .*

381. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR594673 (Variovorax sp. PBL-E5 plasmid 3) position: , mismatch: 8, identity: 0.733

catacc---gccgcccatgccgccgcccatacc	CRISPR spacer
---atccgagccgcccttgccgccgcccatcgg	Protospacer
   *.*   ******* *************

382. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_016586 (Azospirillum lipoferum 4B plasmid AZO_p2, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
aataccgccggccatgccgcctccaggtca	Protospacer
 ********* ********** ** .  *

383. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP024423 (Paracoccus yeei strain TT13 plasmid pTT13-1, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tctgccgccgcccttgccgccgccccggcg	Protospacer
. *.********* ***********  .*

384. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP007796 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p3, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccgccgccgcccttgccgccgcccgagcc	Protospacer
  ..********* ***********. .**

385. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
accaccgccgccccggccgccgcccagccg	Protospacer
  .**********  ***********  *

386. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cattccgccgcccatgccgcctgcggccac	Protospacer
*** *****************  * ..  *

387. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP040819 (Paraoceanicella profunda strain D4M1 plasmid pD4M1A, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gaacttgccgcccatgccgccgccgatggc	Protospacer
 *  ..****************** **. *

388. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_013852 (Allochromatium vinosum DSM 180 plasmid pALVIN01, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
cgattcgccgcccatgccgtcgccgataag	Protospacer
*.  .**************.**** ***

389. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP025547 (Mycobacterium paragordonae strain 49061 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccaccgccgccgaagccgccgcccaatgc	Protospacer
  .********* * ***********   *

390. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
caccccgccgcccatcccgccgcccgcctg	Protospacer
**. *********** *********.. .

391. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_009620 (Sinorhizobium medicae WSM419 plasmid pSMED01, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ctccttgccgccgaagccgccgcccatacg	Protospacer
* . ..****** * **************

392. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_014007 (Sphingobium japonicum UT26S plasmid pCHQ1, complete sequence) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gagtgcgccgaccatgccgccgcccaggtc	Protospacer
 *   ***** *************** ..*

393. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MG872834 (Gordonia phage Confidence, complete genome) position: , mismatch: 8, identity: 0.733

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gaaaccgccgaccatgccgccgccgtagct	Protospacer
 * ******* *************   .*.

394. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN693998 (Marine virus AFVG_250M48, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
accgccgccgcccatgccaccacccatcat	Protospacer
  ..**************.**.*****  .

395. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_010510 (Methylobacterium radiotolerans JCM 2831 plasmid pMRAD01, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gatgccgccgcccatgccgccggcggacag	Protospacer
 **.****************** * .

396. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP029357 (Azospirillum sp. CFH 70021 plasmid unnamed2) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
atccccgccgcccatgccgccggcctcggc	Protospacer
  . ****************** ** .. *

397. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_017958 (Tistrella mobilis KA081020-065 plasmid pTM3, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccgccgccgcctatgccgccgcccgggcg	Protospacer
  ..********.************. .*

398. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to CP000662 (Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA01, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
accaccgccgcccttgccgccgccctgcgt	Protospacer
  .********** ***********    .

399. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR594669 (Variovorax sp. SRS16 plasmid 4) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gagcgcgccgcccatgccgccggccagcgt	Protospacer
 *   ***************** ***   .

400. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP011518 (Pandoraea oxalativorans strain DSM 23570 plasmid pPO70-1, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gaccacgccgcccatgccgccggccaccgt	Protospacer
 *.  ***************** ***.  .

401. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to CP000663 (Rhodobacter sphaeroides ATCC 17025 plasmid pRSPA02, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccgccgccgcccatgccgcggcgcatctg	Protospacer
  ..**************** ** *** .

402. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP021819 (Sinorhizobium meliloti strain M162 plasmid psymA, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccaccgccgcccatgccgccaccggtcga	Protospacer
  .******************.** .*

403. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP031752 (Rhodobacter sphaeroides strain EBL0706 plasmid p.A, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccgccgccgcccatgccgcggcgcatctg	Protospacer
  ..**************** ** *** .

404. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR594673 (Variovorax sp. PBL-E5 plasmid 3) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gagcgcgccgcccatgccgccggccagcgt	Protospacer
 *   ***************** ***   .

405. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to CP000385 (Mycobacterium sp. MCS Plasmid1, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gctggtgccgcccatgccgccacccatggg	Protospacer
  *. .***************.*****.

406. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_008704 (Mycobacterium sp. KMS plasmid pMKMS02, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gctggtgccgcccatgccgccacccatggg	Protospacer
  *. .***************.*****.

407. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP021082 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI1, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggccgcgccgaccatgccgccgcccaccac	Protospacer
 ..  ***** ***************.  *

408. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP039892 (Agrobacterium tumefaciens strain CFBP5499 plasmid pAtCFBP5499c, complete sequence) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gatatcgccgcccatgccgccgaagttcgg	Protospacer
 ***.*****************    *

409. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK820641 (Gordonia phage EnalisNailo, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

410. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK284520 (Gordonia phage Lilas, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

411. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN062715 (Gordonia phage Marteena, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

412. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK433275 (Gordonia phage EMsquaredA, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

413. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to KC661275 (Mycobacterium phage HINdeR, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccgttaccgcccatgccgccgcccgcacc	Protospacer
  .....******************..***

414. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MK433274 (Gordonia phage Bradissa, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

415. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MH513979 (Gordonia phage Pollux, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

416. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MT521999 (Gordonia Phage Jablanski, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

417. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_030942 (Gordonia phage BritBrat, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggaaccgccgaccatgccgccgccgtagct	Protospacer
 . ******* *************   .*.

418. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to KC117377 (Halovirus HVTV-1, complete genome) position: , mismatch: 9, identity: 0.7

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
agcgagacctcccatgccgccgcccatgcc	Protospacer
 ...  .** *****************.**

419. spacer 12.1|2859742|33|NZ_CP036292|CRISPRCasFinder matches to NZ_CP015231 (Epibacterium mobile F1926 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.697

gggacgcaagtcccaggaaatcgccctccatcg	CRISPR spacer
tgctgagcagtccctggaaatagccctccatca	Protospacer
 *   .  ****** ****** **********.

420. spacer 12.1|2859742|33|NZ_CP036292|CRISPRCasFinder matches to NZ_CP015231 (Epibacterium mobile F1926 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.697

gggacgcaagtcccaggaaatcgccctccatcg	CRISPR spacer
tgctgagcagtccctggaaatagccctccatca	Protospacer
 *   .  ****** ****** **********.

421. spacer 12.1|2859742|33|NZ_CP036292|CRISPRCasFinder matches to NZ_CP015231 (Epibacterium mobile F1926 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.697

gggacgcaagtcccaggaaatcgccctccatcg	CRISPR spacer
tgctgagcagtccctggaaatagccctccatca	Protospacer
 *   .  ****** ****** **********.

422. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gtagccgccgcccatcccgccgcccgccat	Protospacer
   .*********** *********..  .

423. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR594669 (Variovorax sp. SRS16 plasmid 4) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
atcgaagccgcccatgccgccgccgatgat	Protospacer
  ..  ****************** **. .

424. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gtccgagccgcccttgccgccgcccatggg	Protospacer
  .   ******* *************.

425. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP029211 (Aquabacterium olei strain NBRC 110486 plasmid pTB101, complete sequence) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gtcggagccgcccttgccgccgcccatggg	Protospacer
  ..  ******* *************.

426. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_LR594673 (Variovorax sp. PBL-E5 plasmid 3) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
atcgaagccgcccatgccgccgccgatgat	Protospacer
  ..  ****************** **. .

427. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gtccgagccgcccttgccgccgcccatggg	Protospacer
  .   ******* *************.

428. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NZ_CP024895 (Amycolatopsis sp. AA4 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
gccgtcgccgcccaggccgccgcccacgga	Protospacer
  ...********* ***********..

429. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to NC_013859 (Azospirillum sp. B510 plasmid pAB510e, complete sequence) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
ggcgacggcgcccatgccgccgcccagctt	Protospacer
 ... ** ******************  ..

430. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to KT870145 (Roseobacter phage DSS3P8, complete genome) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
tccgccgccgcccttgccgccgccctgctt	Protospacer
. ..********* ***********   ..

431. spacer 22.2|5447671|30|NZ_CP036292|CRT matches to MN602268 (Bacteriophage DSS3_MAL1, complete genome) position: , mismatch: 10, identity: 0.667

cataccgccgcccatgccgccgcccatacc	CRISPR spacer
accaccgccgcccttgccgccgccgccgtt	Protospacer
  .********** **********  ....

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

414758 : 488353

Trichoplusia_ni_ascovirus(16.67%)

tRNA,transposase,protease

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_145117364.1\|414758_416648_-\|tRNA	tRNA uridine-5-carboxymethylaminomethyl(34) synthesis enzyme MnmG	NA	NA	NA	NA
WP_145117365.1\|416836_418825_+	hypothetical protein	NA	NA	NA	NA
WP_145117366.1\|418925_419879_+\|transposase	Rpn family recombination-promoting nuclease/putative transposase	NA	NA	NA	NA
WP_145117367.1\|419992_421051_+	DNA polymerase III subunit delta	NA	NA	NA	NA
WP_145117368.1\|421334_421517_+	50S ribosomal protein L32	NA	NA	NA	NA
WP_145117369.1\|421609_422542_+	ACP S-malonyltransferase	NA	NA	NA	NA
WP_145117370.1\|422613_423372_+	3-oxoacyl-[acyl-carrier-protein] reductase	Q06VL0	Trichoplusia_ni_ascovirus	1.6e-16	30.5
WP_145117371.1\|423600_423843_+	acyl carrier protein	B2ZXV3	Ralstonia_phage	2.1e-07	41.7
WP_145117372.1\|424010_425246_+	beta-ketoacyl-ACP synthase II	NA	NA	NA	NA
WP_145117373.1\|425370_427032_+	hypothetical protein	NA	NA	NA	NA
WP_145117374.1\|427045_428593_-	FMN-binding glutamate synthase family protein	NA	NA	NA	NA
WP_145117375.1\|428722_429760_-	ROK family protein	NA	NA	NA	NA
WP_145117376.1\|430020_430545_+	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_145117377.1\|430612_431143_+	hypothetical protein	NA	NA	NA	NA
WP_145117378.1\|431129_431822_+	hypothetical protein	NA	NA	NA	NA
WP_145123958.1\|431858_434651_+	DUF1553 domain-containing protein	NA	NA	NA	NA
WP_145117379.1\|434725_436033_+	DUF1501 domain-containing protein	NA	NA	NA	NA
WP_145117380.1\|436228_438565_-	primosomal protein N'	NA	NA	NA	NA
WP_145117381.1\|438787_440233_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_145117382.1\|440394_442599_-	ATP-binding cassette domain-containing protein	G9BWD6	Planktothrix_phage	2.1e-24	31.1
WP_145117383.1\|442591_443746_-	HlyD family efflux transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_145117384.1\|444236_444836_+	nicotinate-nucleotide adenylyltransferase	NA	NA	NA	NA
WP_145117385.1\|444897_445653_-	TSUP family transporter	NA	NA	NA	NA
WP_145123959.1\|445837_446533_-	FKBP-type peptidyl-prolyl cis-trans isomerase	NA	NA	NA	NA
WP_145117386.1\|446902_447418_-	thiol peroxidase	NA	NA	NA	NA
WP_145117387.1\|447616_447856_-	BON domain-containing protein	NA	NA	NA	NA
WP_145117388.1\|448244_449552_+\|protease	M48 family metalloprotease	NA	NA	NA	NA
WP_145117389.1\|449990_450293_+	hypothetical protein	NA	NA	NA	NA
WP_145089419.1\|450626_451202_+	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_145117390.1\|451280_451703_-	DUF423 domain-containing protein	NA	NA	NA	NA
WP_145117391.1\|451714_452119_-	response regulator	NA	NA	NA	NA
WP_145117392.1\|452405_452807_+	hypothetical protein	NA	NA	NA	NA
WP_145117393.1\|452948_453368_+	hypothetical protein	NA	NA	NA	NA
WP_145089443.1\|453646_453919_+	50S ribosomal protein L28	NA	NA	NA	NA
WP_145117394.1\|453930_454218_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatC	NA	NA	NA	NA
WP_145117395.1\|454348_455830_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA	NA	NA	NA	NA
WP_145117396.1\|455891_457379_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatB	NA	NA	NA	NA
WP_145117397.1\|457488_458289_+	SAM-dependent chlorinase/fluorinase	NA	NA	NA	NA
WP_145117398.1\|458285_458480_+	hypothetical protein	NA	NA	NA	NA
WP_145117399.1\|458534_458993_-	hypothetical protein	NA	NA	NA	NA
WP_145117400.1\|459248_460298_+	low specificity L-threonine aldolase	NA	NA	NA	NA
WP_145117401.1\|460393_461974_+	hypothetical protein	NA	NA	NA	NA
WP_145117402.1\|462073_462622_-	hypothetical protein	NA	NA	NA	NA
WP_145117403.1\|462635_462884_-	hypothetical protein	J9Q735	Salmonella_phage	1.2e-08	41.2
WP_145117404.1\|463049_464033_+\|transposase	Rpn family recombination-promoting nuclease/putative transposase	NA	NA	NA	NA
WP_145117405.1\|464035_464404_+	hypothetical protein	NA	NA	NA	NA
WP_145117406.1\|464450_465518_-	lipid-binding SYLF domain-containing protein	NA	NA	NA	NA
WP_145117407.1\|465648_466941_-	amidohydrolase family protein	NA	NA	NA	NA
WP_145117408.1\|466943_467924_-	aspartate carbamoyltransferase catalytic subunit	A0A1J0F9B8	Only_Syngen_Nebraska_virus	1.7e-31	35.0
WP_145117409.1\|468221_468731_+	hypothetical protein	NA	NA	NA	NA
WP_145117410.1\|468817_470221_-	DUF1552 domain-containing protein	NA	NA	NA	NA
WP_145123960.1\|470265_472911_-	DUF1592 domain-containing protein	NA	NA	NA	NA
WP_145117411.1\|473338_474763_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_145123961.1\|474943_476581_-	ABC transporter permease subunit	NA	NA	NA	NA
WP_145117412.1\|476863_482773_-	hypothetical protein	NA	NA	NA	NA
WP_145117413.1\|482844_484584_+	protein kinase	S4VV57	Pandoravirus	1.0e-18	29.9
WP_145117414.1\|484860_486780_+	hypothetical protein	NA	NA	NA	NA
WP_145117415.1\|486928_488353_-\|transposase	IS4 family transposase	NA	NA	NA	NA

DBSCAN-SWA_2

562039 : 622495

Tupanvirus(16.67%)

tRNA,transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_145117463.1\|562039_562918_-\|transposase	Rpn family recombination-promoting nuclease/putative transposase	NA	NA	NA	NA
WP_145117464.1\|563099_564896_+	elongation factor 4	A0A2K9L6L3	Tupanvirus	2.6e-25	43.9
WP_145123965.1\|564969_566124_+	Gfo/Idh/MocA family oxidoreductase	NA	NA	NA	NA
WP_145123966.1\|566676_567558_+	EamA family transporter RarD	NA	NA	NA	NA
WP_145117465.1\|567645_568386_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_145117466.1\|568541_569624_-	hypothetical protein	NA	NA	NA	NA
WP_145117467.1\|569951_570752_-	hypothetical protein	NA	NA	NA	NA
WP_145117468.1\|571010_572564_-	2-isopropylmalate synthase	E5EQ69	Micromonas_sp._RCC1109_virus	3.1e-06	24.1
WP_145117469.1\|573480_573717_-	addiction module protein	NA	NA	NA	NA
WP_145117470.1\|573983_574868_-\|transposase	IS3 family transposase	A0A0P0I4A4	Acinetobacter_phage	6.4e-49	41.1
WP_145117213.1\|574864_575170_-\|transposase	transposase	NA	NA	NA	NA
WP_145117471.1\|576232_577468_+	VWA domain-containing protein	NA	NA	NA	NA
WP_145123967.1\|578069_579041_+	phosphotransferase	NA	NA	NA	NA
WP_145117472.1\|579209_579455_-	hypothetical protein	NA	NA	NA	NA
WP_145117473.1\|579654_580665_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_145117474.1\|580910_581342_+	hypothetical protein	NA	NA	NA	NA
WP_145117475.1\|581458_583573_-	polyphosphate kinase 1	NA	NA	NA	NA
WP_145117476.1\|584034_585810_-	hypothetical protein	NA	NA	NA	NA
WP_145117477.1\|586156_588466_+	MMPL family transporter	NA	NA	NA	NA
WP_145117478.1\|588477_589554_+	DUF2817 domain-containing protein	NA	NA	NA	NA
WP_145117479.1\|589955_591095_+	hypothetical protein	NA	NA	NA	NA
WP_145117480.1\|591462_592827_+\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_145117481.1\|593325_594501_+	glycosyltransferase	NA	NA	NA	NA
WP_145117482.1\|594544_595447_+	protein kinase	M1HNW7	Paramecium_bursaria_Chlorella_virus	4.4e-13	25.8
WP_145117483.1\|595657_596572_+	protein kinase	W5S595	Pithovirus	2.9e-12	27.8
WP_145089771.1\|596661_597636_+	acetyl-CoA carboxylase carboxyltransferase subunit alpha	NA	NA	NA	NA
WP_145117484.1\|597875_598610_-	CvpA family protein	NA	NA	NA	NA
WP_145117485.1\|598690_599419_+	metal-dependent hydrolase	NA	NA	NA	NA
WP_145117486.1\|600299_601385_-	succinylglutamate desuccinylase/aspartoacylase family protein	NA	NA	NA	NA
WP_145117487.1\|601421_605180_+	mechanosensitive ion channel	NA	NA	NA	NA
WP_145123968.1\|605457_606624_+	magnesium/cobalt transporter CorA	NA	NA	NA	NA
WP_145117488.1\|606729_607179_-\|tRNA	D-tyrosyl-tRNA(Tyr) deacylase	NA	NA	NA	NA
WP_145102565.1\|607553_608261_+	DUF1559 domain-containing protein	NA	NA	NA	NA
WP_145117489.1\|608326_609589_-\|protease	trypsin-like serine protease	A0A1B1IT49	uncultured_Mediterranean_phage	1.4e-17	32.4
WP_145117490.1\|609704_610424_+\|tRNA	leucyl/phenylalanyl-tRNA--protein transferase	NA	NA	NA	NA
WP_145117491.1\|610501_611788_+	amidohydrolase	NA	NA	NA	NA
WP_145089795.1\|612081_612510_+	hypothetical protein	NA	NA	NA	NA
WP_145117492.1\|612496_613552_+\|tRNA	tRNA pseudouridine(13) synthase TruD	NA	NA	NA	NA
WP_145117493.1\|613790_614339_-	hypothetical protein	NA	NA	NA	NA
WP_145117494.1\|614494_614932_-	DUF202 domain-containing protein	NA	NA	NA	NA
WP_145117495.1\|614918_615170_-	hypothetical protein	NA	NA	NA	NA
WP_145123969.1\|615166_616516_-	putative sulfate exporter family transporter	NA	NA	NA	NA
WP_145089811.1\|616696_617206_-	winged helix DNA-binding protein	NA	NA	NA	NA
WP_145117496.1\|617421_618846_+	hydroxyacylglutathione hydrolase	NA	NA	NA	NA
WP_145117497.1\|619136_620753_+	hypothetical protein	NA	NA	NA	NA
WP_145117498.1\|620878_622495_-\|protease	M48 family metalloprotease	NA	NA	NA	NA

DBSCAN-SWA_3

1482756 : 1546918

Sphingobium_phage(25.0%)

terminase,transposase,integrase

attL 1484270:1484287|attR 1515971:1515988

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_145118453.1\|1482756_1484181_+\|transposase	IS4 family transposase	NA	NA	NA	NA
1484270:1484287	attL	NA	NA	NA	NA
WP_145118455.1\|1484286_1486290_-	sulfatase-like hydrolase/transferase	NA	NA	NA	NA
WP_145118457.1\|1486381_1487674_-	class II aldolase/adducin family protein	NA	NA	NA	NA
WP_145118459.1\|1487796_1489287_-	aldehyde dehydrogenase family protein	NA	NA	NA	NA
WP_145118461.1\|1490112_1491306_+\|transposase	transposase	NA	NA	NA	NA
WP_145118463.1\|1491619_1492072_+	hypothetical protein	NA	NA	NA	NA
WP_145118465.1\|1492658_1493549_+	hypothetical protein	NA	NA	NA	NA
WP_145118469.1\|1494337_1494745_+	hypothetical protein	NA	NA	NA	NA
WP_145118471.1\|1494879_1495332_+	hypothetical protein	NA	NA	NA	NA
WP_145118472.1\|1495421_1495988_+	hypothetical protein	NA	NA	NA	NA
WP_145118473.1\|1496102_1496609_+	hypothetical protein	NA	NA	NA	NA
WP_145118475.1\|1497530_1497851_+	hypothetical protein	NA	NA	NA	NA
WP_145118477.1\|1497843_1498401_+\|terminase	terminase small subunit	NA	NA	NA	NA
WP_145118479.1\|1498403_1498637_+	hypothetical protein	NA	NA	NA	NA
WP_145118481.1\|1498891_1499344_+	hypothetical protein	NA	NA	NA	NA
WP_145118483.1\|1499418_1499997_+	hypothetical protein	NA	NA	NA	NA
WP_145118485.1\|1500092_1500311_+	hypothetical protein	NA	NA	NA	NA
WP_145118487.1\|1500357_1502208_+	hypothetical protein	NA	NA	NA	NA
WP_145118489.1\|1503293_1503554_-	hypothetical protein	NA	NA	NA	NA
WP_145118491.1\|1503564_1504149_-	3'-5' exonuclease	A0A1W6DWR2	Sphingobium_phage	3.2e-25	37.1
WP_145118493.1\|1504863_1505064_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_145118495.1\|1505597_1506065_+	hypothetical protein	NA	NA	NA	NA
WP_145118497.1\|1506061_1506418_+	hypothetical protein	NA	NA	NA	NA
WP_145118499.1\|1506911_1507358_+	hypothetical protein	NA	NA	NA	NA
WP_145118501.1\|1507962_1508838_+	hypothetical protein	NA	NA	NA	NA
WP_145118503.1\|1508989_1509205_+	hypothetical protein	NA	NA	NA	NA
WP_145124036.1\|1509288_1509483_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_145118505.1\|1509479_1509827_+	hypothetical protein	NA	NA	NA	NA
WP_145118507.1\|1509981_1510800_+	hypothetical protein	S4V6D4	Staphylococcus_phage	2.5e-07	31.7
WP_145118509.1\|1510796_1512194_+	hypothetical protein	A0A076G7E6	Sinorhizobium_phage	4.1e-26	31.9
WP_145118511.1\|1512316_1513609_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_145118513.1\|1513873_1515856_-	NAD(+) synthase	NA	NA	NA	NA
WP_145118515.1\|1516107_1516797_+	TIGR02453 family protein	NA	NA	NA	NA
1515971:1515988	attR	NA	NA	NA	NA
WP_145118517.1\|1516839_1517580_-	hypothetical protein	NA	NA	NA	NA
WP_145118519.1\|1517572_1518184_-	hypothetical protein	NA	NA	NA	NA
WP_145118521.1\|1521708_1523184_+	hypothetical protein	NA	NA	NA	NA
WP_145118523.1\|1523465_1525487_+	hypothetical protein	NA	NA	NA	NA
WP_145091005.1\|1525709_1525874_+	50S ribosomal protein L33	NA	NA	NA	NA
WP_145118525.1\|1525900_1527652_+	single-stranded-DNA-specific exonuclease RecJ	A7KV88	Bacillus_phage	4.3e-65	29.4
WP_145124037.1\|1527762_1528494_-	DUF1080 domain-containing protein	NA	NA	NA	NA
WP_145118527.1\|1528901_1530584_-	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_145118529.1\|1530650_1531301_-	hypothetical protein	NA	NA	NA	NA
WP_145118531.1\|1531612_1532524_+	thiamine-monophosphate kinase	NA	NA	NA	NA
WP_145118533.1\|1533520_1533796_-	30S ribosomal protein S20	NA	NA	NA	NA
WP_145118535.1\|1533924_1535421_+	uroporphyrinogen-III C-methyltransferase	NA	NA	NA	NA
WP_145118537.1\|1535472_1536276_-	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_145118539.1\|1536422_1537022_-	DUF3299 domain-containing protein	NA	NA	NA	NA
WP_145118541.1\|1537053_1537734_-	DUF3299 domain-containing protein	NA	NA	NA	NA
WP_145118543.1\|1539494_1540307_-	TSUP family transporter	NA	NA	NA	NA
WP_145118545.1\|1540498_1541338_+	iron export ABC transporter permease subunit FetB	NA	NA	NA	NA
WP_145118547.1\|1541461_1541929_-	hypothetical protein	NA	NA	NA	NA
WP_145118549.1\|1542232_1543408_+	hypothetical protein	NA	NA	NA	NA
WP_145118551.1\|1543761_1545147_+\|transposase	transposase	NA	NA	NA	NA
WP_145117480.1\|1545553_1546918_+\|transposase	IS4 family transposase	NA	NA	NA	NA

DBSCAN-SWA_4

3038395 : 3075992

Cronobacter_phage(25.0%)

transposase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_145120410.1\|3038395_3039643_-\|transposase	transposase	NA	NA	NA	NA
WP_145120412.1\|3040298_3041861_-	sulfatase-like hydrolase/transferase	NA	NA	NA	NA
WP_145120414.1\|3042027_3042885_-	hypothetical protein	NA	NA	NA	NA
WP_145120416.1\|3043060_3044518_+	hypothetical protein	NA	NA	NA	NA
WP_145120418.1\|3044720_3044936_-	hypothetical protein	NA	NA	NA	NA
WP_145120420.1\|3045440_3046415_+	aldo/keto reductase	NA	NA	NA	NA
WP_145124111.1\|3046709_3047834_+	aminotransferase class V-fold PLP-dependent enzyme	NA	NA	NA	NA
WP_145120422.1\|3047848_3048823_-	hypothetical protein	NA	NA	NA	NA
WP_145124112.1\|3049597_3050347_+	glycosyltransferase	F1C5B0	Cronobacter_phage	4.3e-06	27.2
WP_145120424.1\|3050417_3051245_+	alpha/beta hydrolase	NA	NA	NA	NA
WP_145120426.1\|3052917_3053463_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_145120428.1\|3053459_3054158_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_145120430.1\|3054154_3054571_-	hypothetical protein	NA	NA	NA	NA
WP_145120432.1\|3054759_3055062_-	hypothetical protein	NA	NA	NA	NA
WP_145120434.1\|3055067_3055385_+\|transposase	transposase	NA	NA	NA	NA
WP_145124113.1\|3055634_3056627_+	hypothetical protein	NA	NA	NA	NA
WP_145120436.1\|3057612_3057918_+	hypothetical protein	NA	NA	NA	NA
WP_145124114.1\|3058052_3058280_+\|transposase	transposase	NA	NA	NA	NA
WP_145120438.1\|3058276_3059155_+\|transposase	IS3 family transposase	A0A0P0I4A4	Acinetobacter_phage	4.5e-31	32.7
WP_145120440.1\|3059557_3063313_+	hypothetical protein	NA	NA	NA	NA
WP_145124115.1\|3063525_3064782_-\|transposase	IS256 family transposase	A0A2P1JQX9	Mycobacterium_phage	1.5e-107	49.4
WP_145120442.1\|3065586_3066345_+	hypothetical protein	NA	NA	NA	NA
WP_145120443.1\|3066900_3068913_+	Na+:solute symporter	NA	NA	NA	NA
WP_145120445.1\|3069447_3070581_+	AI-2E family transporter	NA	NA	NA	NA
WP_145120447.1\|3070820_3071645_+	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_145120449.1\|3071816_3074399_-	ATP-dependent helicase HrpB	A0A2H4UU36	Bodo_saltans_virus	4.2e-32	27.6
WP_145120451.1\|3074567_3075992_-\|transposase	IS4 family transposase	NA	NA	NA	NA

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_CP036292

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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