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_CP036280	Planctomycetes bacterium Pan265 chromosome, complete genome	9 crisprs	csa3,WYL,cas3,DinG,cas2,cas1,cas4,cas7,cas8c,cas5	0	22	3	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP036280_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_1

733412-733538

Orphan

Consensus_repeat	Method
CGTCGACCTGCTCGACCTCTCGGCCCTCGCCTCCAACTTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036280_1

>merge|NZ_CP036280|1|733412-733538|CRISPRCasFinder
CGTCGACCTGCTCGACCTCTCGGCCCTCGCCTCCAACTTCAACGCCGTCGCCGGCTGGGCGGGCGGCAACTTCAACACCGACACCGTCGTCGACCTGCTCGACCTCTCGGCCCTCGCCTCCAACTTC

>NZ_CP036280|1|1|733412-733538|CRISPRCasFinder
CGTCGACCTGCTCGACCTCTCGGCCCTCGCCTCCAACTTC	AACGCCGTCGCCGGCTGGGCGGGCGGCAACTTCAACACCGACACCGT
CGTCGACCTGCTCGACCTCTCGGCCCTCGCCTCCAACTTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145444895.1\|736527_737970_+\|sialate-O-acetylesterase	unknown	unknown	gnl\|CDD\|377084
NZ_CP036280.1\|WP_145444898.1\|741531_742389_-\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|377877
NZ_CP036280.1\|WP_145444902.1\|749396_751265_+\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|271213
NZ_CP036280.1\|WP_145444891.1\|729573_730821_-\|alginate-lyase-family-protein	unknown	unknown	gnl\|CDD\|377511
NZ_CP036280.1\|WP_145444899.1\|742534_745699_-\|DUF4981-domain-containing-protein	unknown	unknown	gnl\|CDD\|236548
NZ_CP036280.1\|WP_145444886.1\|721437_724536_+\|DUF2339-domain-containing-protein	unknown	unknown	gnl\|CDD\|227665
NZ_CP036280.1\|WP_145447201.1\|725272_726475_-\|starvation-sensing-protein-RspA	unknown	unknown	gnl\|CDD\|239438
NZ_CP036280.1\|WP_145444897.1\|740354_741434_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271213
NZ_CP036280.1\|WP_145444894.1\|734713_736531_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271371
NZ_CP036280.1\|WP_145447202.1\|745841_747050_-\|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl\|CDD\|377028
NZ_CP036280.1\|WP_145444889.1\|727456_728518_-\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036280.1\|WP_145444901.1\|748129_749335_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|225076
NZ_CP036280.1\|WP_145444890.1\|728542_729535_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381311
NZ_CP036280.1\|WP_145444884.1\|718358_720053_+\|PQQ-dependent-sugar-dehydrogenase	unknown	unknown	gnl\|CDD\|369642
NZ_CP036280.1\|WP_145444887.1\|724643_725195_+\|fasciclin-domain-containing-protein	unknown	unknown	gnl\|CDD\|225214
NZ_CP036280.1\|WP_145444885.1\|720128_721274_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|223699
NZ_CP036280.1\|WP_145444888.1\|726518_727424_-\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|224007
NZ_CP036280.1\|WP_145444900.1\|747334_748075_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376421
NZ_CP036280.1\|WP_145444892.1\|731046_732144_+\|substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|224525
NZ_CP036280.1\|WP_145444896.1\|737990_740354_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271210

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145444895.1\|736527_737970_+\|sialate-O-acetylesterase	gnl\|CDD\|377084	pfam03629, SASA, Carbohydrate esterase, sialic acid-specific acetylesterase. The catalytic triad of this esterase enzyme comprises residues Ser127, His403 and Asp391 in UniProtKB:P70665.	1.22063e-17
NZ_CP036280.1\|WP_145444898.1\|741531_742389_-\|PEP-CTERM-sorting-domain-containing-protein	gnl\|CDD\|377877	pfam07589, VPEP, PEP-CTERM motif. This motif has been identified in a wide range of bacteria at their C-terminus. It has been suggested that this is a protein sorting signal. Based on phylogenetic profiling it has been suggested that the EpsH family of proteins mediate this function.	0.00194942
NZ_CP036280.1\|WP_145444902.1\|749396_751265_+\|PEP-CTERM-sorting-domain-containing-protein	gnl\|CDD\|271213	cd14254, Dockerin_II, Type II dockerin repeat domain. Bacterial cohesin domains bind to a complementary protein domain named dockerin, and this interaction is required for the formation of the cellulosome, a cellulose-degrading complex. The cellulosome consists of scaffoldin, a noncatalytic scaffolding polypeptide, that comprises repeating cohesion modules and a single carbohydrate-binding module (CBM). Specific calcium-dependent interactions between cohesins and dockerins appear to be essential for cellulosome assembly. This subfamily represents type II dockerins, which are responsible for mediating attachment of the cellulosome complex to the bacterial cell wall.	2.67462e-06
NZ_CP036280.1\|WP_145444891.1\|729573_730821_-\|alginate-lyase-family-protein	gnl\|CDD\|377511	pfam05426, Alginate_lyase, Alginate lyase. This family contains several bacterial alginate lyase proteins. Alginate is a family of 1-4-linked copolymers of beta -D-mannuronic acid (M) and alpha -L-guluronic acid (G). It is produced by brown algae and by some bacteria belonging to the genera Azotobacter and Pseudomonas. Alginate lyases catalyze the depolymerization of alginates by beta -elimination, generating a molecule containing 4-deoxy-L-erythro-hex-4-enepyranosyluronate at the nonreducing end. This family adopts an all alpha fold.	2.69178e-84
NZ_CP036280.1\|WP_145444899.1\|742534_745699_-\|DUF4981-domain-containing-protein	gnl\|CDD\|236548	PRK09525, lacZ, beta-galactosidase.	0
NZ_CP036280.1\|WP_145444886.1\|721437_724536_+\|DUF2339-domain-containing-protein	gnl\|CDD\|227665	COG5373, COG5373, Predicted membrane protein [Function unknown].	1.28463e-54
NZ_CP036280.1\|WP_145447201.1\|725272_726475_-\|starvation-sensing-protein-RspA	gnl\|CDD\|239438	cd03322, RspA, The starvation sensing protein RspA from E.coli and its homologs are lactonizing enzymes whose putative targets are homoserine lactone (HSL)-derivative. They are part of the mandelate racemase (MR)-like subfamily of the enolase superfamily. Enzymes of this subfamily share three conserved carboxylate ligands for the essential divalent metal ion (usually Mg2+), two aspartates and a glutamate, and catalytic residues, a partially conserved Lys-X-Lys motif and a conserved histidine-aspartate dyad.	5.17114e-157
NZ_CP036280.1\|WP_145444897.1\|740354_741434_-\|hypothetical-protein	gnl\|CDD\|271213	cd14254, Dockerin_II, Type II dockerin repeat domain. Bacterial cohesin domains bind to a complementary protein domain named dockerin, and this interaction is required for the formation of the cellulosome, a cellulose-degrading complex. The cellulosome consists of scaffoldin, a noncatalytic scaffolding polypeptide, that comprises repeating cohesion modules and a single carbohydrate-binding module (CBM). Specific calcium-dependent interactions between cohesins and dockerins appear to be essential for cellulosome assembly. This subfamily represents type II dockerins, which are responsible for mediating attachment of the cellulosome complex to the bacterial cell wall.	6.19318e-06
NZ_CP036280.1\|WP_145444894.1\|734713_736531_+\|hypothetical-protein	gnl\|CDD\|271371	cd11477, SLC5sbd_u1, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	9.70391e-91
NZ_CP036280.1\|WP_145447202.1\|745841_747050_-\|endonuclease/exonuclease/phosphatase-family-protein	gnl\|CDD\|377028	pfam03372, Exo_endo_phos, Endonuclease/Exonuclease/phosphatase family. This large family of proteins includes magnesium dependent endonucleases and a large number of phosphatases involved in intracellular signalling. This family includes: AP endonuclease proteins EC:4.2.99.18, DNase I proteins EC:3.1.21.1, Synaptojanin an inositol-1,4,5-trisphosphate phosphatase EC:3.1.3.56, Sphingomyelinase EC:3.1.4.12, and Nocturnin.	2.5107e-12
NZ_CP036280.1\|WP_145444889.1\|727456_728518_-\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	7.3916e-56
NZ_CP036280.1\|WP_145444901.1\|748129_749335_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|225076	COG2165, PulG, Type II secretory pathway, pseudopilin PulG [Cell motility and secretion / Intracellular trafficking and secretion].	2.72247e-08
NZ_CP036280.1\|WP_145444890.1\|728542_729535_-\|aldo/keto-reductase	gnl\|CDD\|381311	cd19085, AKR_AKR11B3, Synechococcus sp. aldo-keto reductase (SakR1) and similar proteins. Synechococcus sp. SakR1 is a founding member of aldo-keto reductase family 11 member B3(AKR11B3). It is responsible for methylglyoxal detoxification.	2.88121e-130
NZ_CP036280.1\|WP_145444884.1\|718358_720053_+\|PQQ-dependent-sugar-dehydrogenase	gnl\|CDD\|369642	pfam07995, GSDH, Glucose / Sorbosone dehydrogenase. Members of this family are glucose/sorbosone dehydrogenases that possess a beta-propeller fold.	1.15857e-24
NZ_CP036280.1\|WP_145444887.1\|724643_725195_+\|fasciclin-domain-containing-protein	gnl\|CDD\|225214	COG2335, COG2335, Secreted and surface protein containing fasciclin-like repeats [Cell envelope biogenesis, outer membrane].	9.37571e-47
NZ_CP036280.1\|WP_145444885.1\|720128_721274_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|223699	COG0626, MetC, Cystathionine beta-lyases/cystathionine gamma-synthases [Amino acid transport and metabolism].	0
NZ_CP036280.1\|WP_145444888.1\|726518_727424_-\|TIM-barrel-protein	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	3.63157e-21
NZ_CP036280.1\|WP_145444900.1\|747334_748075_+\|hypothetical-protein	gnl\|CDD\|376421	pfam00932, LTD, Lamin Tail Domain. The lamin-tail domain (LTD), which has an immunoglobulin (Ig) fold, is found in Nuclear Lamins, Chlo1887 from Chloroflexus, and several bacterial proteins where it occurs with membrane associated hydrolases of the metallo-beta-lactamase,synaptojanin, and calcineurin-like phosphoesterase superfamilies.	2.97477e-11
NZ_CP036280.1\|WP_145444892.1\|731046_732144_+\|substrate-binding-domain-containing-protein	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	6.751e-55
NZ_CP036280.1\|WP_145444896.1\|737990_740354_+\|hypothetical-protein	gnl\|CDD\|271210	cd14251, PL-6, Polysaccharide Lyase Family 6. Polysaccharide Lyase Family 6 is a family of beta-helical polysaccharide lyases. Members include alginate lyase (EC 4.2.2.3) and chondroitinase B (EC 4.2.2.19). Chondroitinase B is an enzyme that only cleaves the beta-(1,4)-linkage of dermatan sulfate (DS), leading to 4,5-unsaturated dermatan sulfate disaccharides as the product. DS is a highly sulfated, unbranched polysaccharide belonging to a family of glycosaminoglycans (GAGs) composed of alternating hexosamine (gluco- or galactosamine) and uronic acid (D-glucuronic or L-iduronic acid) moieties. DS contains alternating 1,4-beta-D-galactosamine (GalNac) and 1,3-alpha-L-iduronic acid units. The related chondroitin sulfate (CS) contains alternating GalNac and 1,3-beta-D-glucuronic acid units. Alginate lyases (known as either mannuronate (EC 4.2.2.3) or guluronate lyases (EC 4.2.2.11) catalyze the degradation of alginate, a copolymer of alpha-L-guluronate and its C5 epimer beta-D-mannuronate.	9.49177e-151

>NZ_CP036280.1|WP_145444892.1|731046_732144_+|substrate-binding-domain-containing-protein
MSIVDVAKLAGLSHTTVSRVINHQPGVSASTVKKVQQAMRQLGYTPPARRRGPQPRHRRNIRTGNIALLMFGTDAAPMIAPVAAAVTHYLEEHLGRHDLNLSIGQVKSDGRIPSAVANGRVDGLILHGRPPSPEVAAKLMRFPSVWIMSPRSRTGYWGDRVCPDNSAIGRIAAEYLIGRGHDRISMLEIETAHLGFRERAMAFCETAEEHNVSTELITVPDQDDSQAQGSPMRPAMINALIDRFVALEDRPSGLFVPLGQATLAVYEALRMRGIEPGGQVTVVACDNDPTLAGLNPRLATVDVRPDRIGQLAVEQLLLRMDKASPHARTQVLVEPSLVTPPVPEEPRIPASEITTSNGVRTPSFA
>NZ_CP036280.1|WP_145444891.1|729573_730821_-|alginate-lyase-family-protein
MVTMPRFTPLLVLVAALLHAMLVSPAVMAQDLPQVYITDPARLAAVRERVRAGDPSLQRAMDELILLAEASMDKPMISVVEKPKAPPSGDFNDYVSLSPYWWPDPSKPDGLPYIRRDGEINPERYEYDVDKLGTFGETVRWLGFAYYFTGEERYAREAVKRVRHFLLDPETRMNPRVQYGQFIPGRNEGRKYGIIETLRLRWVPDAISLLAESEAMTEEDLAGARQWFADYARWLDTSEFGVGEREGPNNHGTWCTAQTAYFALAGGDEELVRKMAALIPDRIAAQIEPDGRQPHELARTRAMDYSEFNLRGHTEMAVLAERVGIDLWSFETEDGRSLERAYAFLMPYLSGEKPWPYKQISDPKHDYYAQSLRRMAIATNDPVYEETVASLSDLTGAGRVYLDLIISLPEDFPKP
>NZ_CP036280.1|WP_145444890.1|728542_729535_-|aldo/keto-reductase
MQYMELGDSGLKVSRIAFGSMSIVANPTYSGVEETQAIEAIHTAYDAGINFFDTAPGYGNGAAEVVLGRALAGGLREKVIVADKINTPSLTAQDVETEFALACERLNTDYIDLYQIHWPKNVVPVEETLRAMENLVTSGRVRSLGVSNFGPVDLTEALGVCSLVSNQIAYNLLNRAPEFEVVEIMLKHNMGMLCYSPIAQGLLAGKFSNADEVPDERARTRIFASTRPQARHSEPGCETEAFEAIAGVRAVAERVGQSMADVSIAWLLAQPTVTSVLVGASMPEQVKRNAAAADVKLSQQDLDELSSITESVKQILGPNMDVWQTESRIR
>NZ_CP036280.1|WP_145444889.1|727456_728518_-|Gfo/Idh/MocA-family-oxidoreductase
MIQQQDSSSGLSPLRVGVIGLGRSGFNIHCKWLSTLPEHFAVAAVADPDRHRCQEARQTFGAQVHNSVDDLIHDGSLDVVVVASPNLMHEEQACSAMQAGRHVVVEKPLALSTQGADRMIACAEETGRVLAPFQNRRFEPHFRKVREVLGSGILGRIVQIRIEWSFFTRRWDWQTLRSQGGGSLHNHGAHLLDHALELFGEGDPEVFVDMQHALSMGDAEDHVKVILRGEGHPTIDIESSSCCVFPEDRWHVWGTAGGLRGTTDRLEWRWVDWNTMPERHADEGPAEGRAYQHEAYEWQSASWEDPKDEPITAVLFYRNLLDVLRGRGTLTVTPESVRRQMAVLDQCHAQMAC
>NZ_CP036280.1|WP_145444888.1|726518_727424_-|TIM-barrel-protein
MPTVTQATQPEMYASLMTDMVGARMTPDVGAYLAARHGFPGLDLRLNAYADFLDTFGVERFADLLEERGIRPGYVSITTRTLSASDGEWAEMMRLLPERAKTAQRLGYTRAGVVMLPFDDERDTAANHRRHVVRIRQVAPVLADHDIRLGVEYVAPVTRRRGHPHPFIHNMRGTLRLLHDAGQPNVGLMLDTLHWATAGESVEDIEALEADQVVVVHVCDGIRGRAIEAQTVHERELPGATGVYDNAGFIEALRTIGYTGPVTAEPSHPRWASTDPELAVAQTARAVLDTLCRTEAPQPES
>NZ_CP036280.1|WP_145447201.1|725272_726475_-|starvation-sensing-protein-RspA
MGRNLLVARVDTSEPELYGLGCGTFTQRYLPVRSAIVDYLRPLLLGREAARIEELWRLMMVNSYWRHGPVLNNAVSAIDMALWDIKGKVAGLPIYELFGGKMREAAAVYQHADGRSLDELTEHVRAQLDQGMSHVRIRFGGGSAETRNSGEAGGMAYGGAAERPIHKPDGALDGAYFDPVQYTRSTITAFDHVRSTFGDQVELLHDVHGRLAPAEAIAFAREMERFRLFFLEDALPPEDIGWYERMRGATTTPQAVGELFNNPNEWLPLVSNRWIDFIRMHISQLGGLTPARKAATVAEAFGVRAAWHGPGDLSPVGHMANLHLNLTLPNFGVQELQPFTDTTREVFPGCPEFRDGYLYPNNAPGFGVDLDEKLAERFPCDPAVVQWTQARYPDGGLSRP
>NZ_CP036280.1|WP_145444887.1|724643_725195_+|fasciclin-domain-containing-protein
MRAITTGTLALTAASMLAFAATPVMACSSCGCSSSDGHDKKKADIVDTAVSAGKFKTLVAAVTTAELVSVLKSDGPFTVLAPTDAAFDKLPHGTVDSLLKPENREQLVSILTYHVIAGEIEASAAIKAGEATTLQGGELEFSVESADGKLMAMVNDINIVYTDIETSNGIIHVIDEVLIPEAE
>NZ_CP036280.1|WP_145444886.1|721437_724536_+|DUF2339-domain-containing-protein
MPVEALIVVVVLITVISVPLCVIYLLIANASARRRLDELEHELRLVRARMNQALPPPTPPTPESISSQPVAETSPSRTERLHEVLAERRAQATAESQSVAETPISPPESQTAEGSPPEAAETTSPIADDLDESVIVTSDESEDDDTPGERPSPESLEDVLGSRIFVWIGGIAIALGGAFLVKYSWDNDLLSAQVRLSIGALIALMCTGVGYWMKPRAERVAAALVGAGIAIAYGVTFAATSVYHFLGPTSGFILMGLITAAAVMLSLRHGMYVAMLALLGGFVTPVLVGDSDGSMAGLFAYLIVLQTGLVVVTRRRGWIGISGLTLVGSIVWSVVMALTGLGGPDGTFWGGLLLVASCVVYVLHAARAEASTQQQSLLTPLRLAMGAIGASAALLGILLASSGYDPSTLIMLAVLSAGSLALAHFDARYRAIPWLTLVIAWLMLLGVNHDLDADSLRRIALLFGGLFSSGACLSLLLGRHRRELILMSCVGLMLFVALVALIRPVEEQAPLLLWWVMTIIAGAYALLAWVMRGRYREAAGGLALTVVAWLTWAASRGIELPWTVLAWSLLAVAACMLAPRLRMMRYLRWSLAWLLPLIGSFLLVAITRQSWATPGTTSMIYYVPSLLIGLAALQMHRRRQMFARDVLSVMAVLLSLIGSLRLVHQVFHGKMTEQPPEGLTEWGCYVLLLLVYPTAMLLIDRWRSLTSTLTQLAKILSGLAAATTLAALALFANPIILDVDLAGGIIFNEATLFYGLAAALLLWLSQERIMRTEAGAIWLGIIGLSLIGWLGVVLIRDGFAGENSLVWTPLSASEWTTHTLWFIALAFIAQRQRFADHIPALNRMLPVYLLIGLAAGAGCLSFGNPLWLDQANGSWPVLNAVLYAYGTPVVAFAFATRYFNSITRPVPFGPTFAVSSLVMLFVLVTLQVRHAFTGGAMLIENDLINRTEWYAYSVAWLALGAALLTTGLLVHSRALRFGSLIVVLLAVGKVFLLDTTQLDGLYRVASFFGLGLSLLAVGYVYQRFVFGRPVSS
>NZ_CP036280.1|WP_145444885.1|720128_721274_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MKQKTEAIHAGVYQDKTWGSVTTPIYPSSTFTFPKLGEHPVFDYTRSGNPTRAGLEESLAALEGGKVALATSTGMSAITTTLFLFQSGDHVIAGNDIYGGTYRLFDAIMPKMGINFTFVDMRDPDAVRAAIRPETKGLWIETPSNPLLNITDVKAMTAIAREHKLLTIADNTFLSPVFQRPLDLGVDIVLHSTTKYINGHSDVVGGAVIAADPEIGQRVRDAGNAIGTACSPFDAFLVLRGIKTLPVRMAEHARNAQVIAAWLEKHPRVQRVYYPGLDSHPQKALIDQQMLGPGGMLSFDLDADEQQIPAFYGALELFLLAESLGGVESLVEQPWSMSHASMGPDGLAASGITPQTVRVSVGLEATEDLIADLERGFAAIG
>NZ_CP036280.1|WP_145444884.1|718358_720053_+|PQQ-dependent-sugar-dehydrogenase
MGMKSLSVAASLLITGGYALAQTNPIIPVVPKTPWKVVLEEVVTIPDSLGTYPRLEELTHAPGSDDAFVLDQNGTIYRFDPYAANPTPQVFLDLNSAVPAGFRTGSQEGLRGLAFHPDFATPGTDGYRKFYTSHSRSAFTGIYFGDGVTPVIYGAPGGVDHDAYVAEWSVNPDGSVDTDSYREILLVGQPRADHNIGQIGFDPTAQPGEDDYGNLYITLGDGGGPNDPSNLAQNTSQPHGSILRVDPLRNGSDPFSLPDNPLRTSDSLTNARNLIYAYGVRNPHKFTVDPVTGNFIFSDIGQANIEEINILEPGANYGWDLREGTWTLNSSNVPGTLPPNHPTDSATYPVAQYDHDPENDGVNGSYAVAGGHVYRGSSVPELTGMYLFGDFGTNPGPIYAVDADDLTQRDDFTDIDQIFGGYLAPLVELTLNTEGDATDKTFLDIVKETNPFIPRTDLRFGIDAAGEIYILSKRDGKVRRISAVIGLLAGDANRDGIVDLLDLSLLASGFDGPGDWGSGDFNADGLVNLLDLSLLASNFGQTSIPQPAVGLIMLTMLSGFRRGA
>NZ_CP036280.1|WP_145444894.1|734713_736531_+|hypothetical-protein
MIEIAVIAGYLLLLVTIGFVLQRLNSDVSDYFRSGCRAKWWMVGSSAFMTAFSAWTFTGGAGAAYTAGLSVTVIFFANVLGFLIQAAFLAGWFRQLRAVTFPEVLRDRFGHLTQQFYAWITVPLQLCYAAVWLWGLATFISSVFGYDINTVILVTGLVVLVYSLFGGSWAVMATDFLQTLILMPITILVTVLCLIELGGITGLIDGIRDAGLASDYAMVNAPDRFDNEDYTWSWLFAVVVYKIINHSALEVSQKYFAVKDGREARQAALLAAVMSFVGVFIWFIPPMAAAILIPDQIEALSLKNAAEGSYALISMNLLPAGLTGVMVVAMFSATMSSMDSGLNRNAAIFTRDMYPTLSRLVGMEPAEGKALLHIGQLFSCAFGFGIIALAYYFAQSEGKGVFQVMLDIGGLLTLPMFIPMLLAIFVRHVPWWSAIFAVLAAFVPSSIAFLSGKYPEYIDWLTPYLPEFLGYMTDGNWTYAQKIFTNTLVGSTAFFITMPFWHGSTDEYRQRADAFYKKMHTPVNFEEEVGEANDDHQRLVVGVFAVVMGSFICLLLLLPNDIKGRLGILFVGGFVLTAGIFLLRSAQRAATAEEPLAPFRGEDNP
>NZ_CP036280.1|WP_145444895.1|736527_737970_+|sialate-O-acetylesterase
MTLRALLILCACCVTATAEITLPALFDDHMVLQQGKPLAVWGRADPRAQVTIEIDTQRVTATTAEDGTWSATLEPLEAGSGYMLRVSADGQSVLFEDVLVGEVWLCSGQSNMDMRMDKMDPSEIEAADHPEIRLFRVERSAVVKPARDVDADWEVCTPENVRDFSAAAYYMGRELQQHLDVPVGLIHTAYGGTAAEAWTRRQVLEANPILVSLVERYERLKADPNATPPEARRIPGGLYNGMIHPLVPYTIRGFAWYQGESNTWRAAQYKTLLEEMIIDWRTQWGDLRLPFAIVQLPGYVNPPRVPAGIYSWEELREAQSRVAYTLPSAGLIVTIDVGDPTDIHPLDKHTVGKRLANWALHTLYEKEIYGLSPRFWEADFRKDSNEVHLKFENVGTGLTTRDGGPVRGFVIAGDDRRFRWAKARIEGDVVIVSEAKVKQPRAVRYAWNENPDWANLVNNEGLPASPFRTDRWPGITDKAR
>NZ_CP036280.1|WP_145444896.1|737990_740354_+|hypothetical-protein
MTRWLVRTSCICVMVSVASAETFFVSSAAQIEDAMDNAAPGDTLVMTDGVWNNQSIDFAGHGTADNPITLRAQSAGGVILTGSSNLSISGSHLVVDGLTFNEGRPSGSHIIRFTGSQGDANHSRLTNTTITNYNPADINDRYFWVSLYGQDNRVDHSRFQGQNHSGVTLVAWLDGDEARHRIDHNHFADRPEGNGNGFETIRIGTSEFGDSSAKVIVENNLFERVDGEVEIISNKSNDNIYRYNTFAESKGTLTLRHGHRANVEGNFFLGKNKDGSGGVRVIGEDHQIINNYFADLDDRMDGVISITAGIENTQPSGYQQVKNALIAHNTIIDAEMPGITFDWGLGERDRTLLAEDVIITGNLILSYADTLFEGNEGPGWTWSDNLVWGAPTGITARPGVTVADTLLQLAPDGLWRPAANSPAIDAIAQANLVTPIDMDGQPRIGLIDIGADEVADAAIVRKPLTSNDVGPDWDNYEPIDPGGPGDPTDPPAGAHIAIEAEQFASVIDPNSDGDTWTVVAAHDAFGGLAIEAPQGDRYNSGSGAHDAIVTYDLTFDEAGNYTAYYRARGFSGSTDSFYHPDALDQDPDQNETTSSNGGWLWETGETFTITDSHLDVPLELRLGKREQTTQIDAIILHINNGLTPGELDALMTRIYEPLSGDFNSDGVLDAADLELVQIAIGTTDTTYDLDDNGIVDAADTHAWLIDAYGTILGDINLDRVVDLLDLSILAANFQTTGLALYTLGDITVDQTVNLLDLSIFASNFGSAATIPSPSTGFFLLCTGLLRR
>NZ_CP036280.1|WP_145444897.1|740354_741434_-|hypothetical-protein
MYQGVSFAVAGLSLLVGTAAASGEVIYSNDFNQHSAGAYTTQMLAADFDAPWEDGVSEGRVAVVDDAEAFSGRSLRVMHVGEDIKLGGKWIMELDRGYEELYASYWVHFGPGTEFVRAGKLPGLAGGEANTGGNKPDGTDGFSARMTWSSNGKDGSQVPTTSANLNQYLYHPDQPQTYGDTRFYDETHDGRWVEVTSGPWYHIQHRVVMNTPGEHDGVVQAWVNGEPVFYVDDIRFRDVPGLQIDVFRFETFYGGSSMNFATTKEEYFYFDNLVLSTDWRPMALPGDTNLDYAVNLTDLSTLASNFGQPGSWHDGNFDGDGVVGLLDLSLLASNFNSTRIPSPTSAASLLMTLLLTRWR
>NZ_CP036280.1|WP_145444898.1|741531_742389_-|PEP-CTERM-sorting-domain-containing-protein
MKQMKTLIGAMVTFGAFSVAAADVIPLYTEATVAELGDVFNQNVDAGDGVNDYGIEILDAITSPPSPFNDGNAMRMWDFYNGDKPELQGELANPLTGPFRVDFESFNASTNGTSKAIRFRMGNAGDSITSESRVAFSLSWQADKEITAKYENTDDEFKTDSTEPLDGVVDVTIVGNAAVSGNYDYTLFGETRSLAAQSYDVFIDGVLFNDDASKANGLGFTLLKASGNYDPAEGLQRFGLLGSSNGDVDPDVYFDNIILRTGDDIVPEPASLALLSVGALMLRRR
>NZ_CP036280.1|WP_145444899.1|742534_745699_-|DUF4981-domain-containing-protein
MPSAVETLPSFWELPELTHINRLPGRSPLLVYGTSSAALRGDRSRSPWWLSLDGAWRFRMYDRPDAVPAGVTGVKAKDGSWATIPVPSNWTQHGYSSPIYTNVQMPFANTPPEVPKANPTGVYRRDFTIPKVWDGRRIVMHFGGAESVLCVWVNGHWVGMSKDCRLPSEFDVTRFVSPGRNQVTAMVIRWSDASYIEDQDQWWLGGLFREVYLYAQDGAYVEDVFARADYEPKTGAGRLSVDVKLNFVSVPESDVRVQATLFGPDGKAVRGVKMSGVITPDYGAHGNTLTFESDLKRVLPWSAERPDLYALAVSLHEVDARGRARGKGFAYTSCRVGFRRVEVRDRQLLINGQAVMVRGVNRHEHDEVHGKALTEEGMVRDILLMKQNNFNAVRNAHYPNDPRWYALCDQYGLYVIDEANIEAHANYHTLCRDPRWRGAFVDRVANMARRTKNHACVILWSLGNETGYGENHDEAARWLRGYDPTRPLHYEGGVRVSWTQGPNAKYAVGRDVTDVFCPMYPSVDEMVAWSERGNDDRPYIPCEYQHAMGNSNGCLKEYWEAFESCDGLQGGFIWEWVDHGLKRRTEDGTEYWAYGGDFGEKIHDAEFVCDGLVGPDRTPHPAMAECHKLMQPIGFEAGSLRTGRIRVTNKQYFTDLSWLALTWFVEVEGRRVASGRLDRSLGKLRPQQSATATLDYDAATLPAGEAFLTIQARAAKKTAWCGKGHLVGWEQFALPVKARLRAPVRRRRGVVACRETQRKLVLTCPSRGVELTVDRRAGVLKSLAVEGQPVVLEGPRLNVWRGPTSNDGIKGWTDYRDSDRRTAGRWFLAGLDRIERSVAAEPKLVRRRDGSVRMTLRQHWTSTGRDGMVHGLSDQQVYTVLPDGSVRVTHAFDLDATLPELPRVGVVLSFAAGFERLSWFGRGPGESYPDRKAGMPVGLYRSTVDEQFVPYIVPQEHGLKTDVRWMSLGHESGRGVRIEAGDATSPVSFSASHYTPHDLTEARHVHELRRRDEVIVCIDAAHRGLGTASCGPDTLDRYLVRPGRYRLSYDLTAR
>NZ_CP036280.1|WP_145447202.1|745841_747050_-|endonuclease/exonuclease/phosphatase-family-protein
MRFTVVCVVLSVASWASAQPVPGPAGVVSGEGERPHFRVATFNASLSREPSGQMLDDLRTGKDPGARRAAEILQRVRPDVVLINEFDRDRRGEALRIFMEFYLHRPQSGQEPIQYPYSYAPEVNTGRLAEVDINGDGKRTLPQDAYGYGRFPGHYGFVVLSRHELRITHARTFQNFLWKDMPGALLPDDASTEAPGDYYSEEVQEHFRLSSKTHVDLPVWIHGRIVHLLVSHPTPPVFDGREDRNGRRNHDEIRFWSDYLSFQESGYIRDDAGRRGGLADGTNFVILGDMNADPFDGDSTQGAVNQLLKHPRVNTSVTPSSRGAELDAEREGRANERHRGEARYDTADFGGPGNLRVDYVLPSKAMKIRRAGVFWPAPLHPLEDLIETSDHRLVWMDLAFTR
>NZ_CP036280.1|WP_145444900.1|747334_748075_+|hypothetical-protein
MCSPNYGGFEKMRTFTLAAAASLALAGAASADLIISEIVDGPLSGGTPKFVELTNTGNAPVDLANYSLGNINNGATTMGFDALVLSGILAAGDSYVVSYENSDAPGASVFFDVYSFDADNLENGSFINGDDVLVLFSGAGLAGDPGNGANVVDVFGVVGVNGDNEPWDYTDSYAVRVPTSITANGGVFNVADFVYGGRDGLEGADDAAETLNLQIFTSPGTHAFIPEPASLAMIALGGLALVRRSA
>NZ_CP036280.1|WP_145444901.1|748129_749335_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MSLNGLTLFYRMLRPVAARYGCRRPTQRRVRRQHPHGLATRRGRGQGAFATLPCTPHGDTPLTNTTDTRPSRAAGFTLIELLVVISIIALLIGILLPALGAARDTARTAIDLGNLRSISQGMFSYSISSKSFLPGPNTSGAHITAGYSDWRQSSTEPTQNMDWISPLFGHALGLSEDRGDRLDDIFNNEFRCPSNTETYNGAVFDAGGVGDVDYENFTVSSYSSPLAFHLWGDNTGANVPLKHGTVASRGNPPPAAEAISLDPGYKGTVDSVGSNSEKVFALDGTRYVDGDGTVTYSGTPRVFQGGNFMVSGPAFADPGGSPYKYNVTGPGKTELTDLAKRYAYRHAGRLNTTFFDGHAKSMDKETAQTVDYFLPTGSVIVNRSATRDSRTPFIENGYVVK
>NZ_CP036280.1|WP_145444902.1|749396_751265_+|PEP-CTERM-sorting-domain-containing-protein
MKTARLLQATLALTAITTAANAVQLPTGGFIAVGDVGNATATSDTVTFYSTDDLSSRLFSVALPFESASNNEDFDALTVNPFTGEVYVTAVDSGTPGTVVTTTDLQTNVQDTDGDLDLYRIDFAAFYNDWVNNQNMADVTYHAEQNDSFFGDPVFSGAPNPIQATGDLGTNGIQKIGEIARSQTFRSNTSDIFNKSLAFIDDDTLVYLDEDTDTSGSVAADHEIRLIKRISGPASYDSNTNEGGFNSNTAESWTSTIVGRVLLDGDTNASEPRTIAGYKDPQSGVTGVWVLEGDGGGDDIGFFEIVDESGDDNGPGGSNLNGYRLATTGLPVFALDNDPANDPTTNDGSGDRVLVNPVTGDLIIMESGFFDSPQHEPSVIQREVVDYDASGEILFGAWSPLLQIDGNQPGDDDTQIVDGRYTAYDHINNVLYYHDRDNPFSGGGGSYDGDWWSINLTTGETKLEATDVGNFQIYDNGTFLGFFSFDQVGIEGDYDNDGELTDADVDLLVNAILAGSTDLTYDANSDGVVDANDYILWRDSLYGTTAGDANLDFVVDLLDLSLLASNFDGPGLHGEGDFNADGLVDLLDLSLLASNFDTGNVPEPAGLALLGLGAAAMLRRQA

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Crispr_ID: NZ_CP036280_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_2

1445565-1445697

Orphan

Consensus_repeat	Method
ACCTGCTCGACCTCTCGATCCTCGCCAGCAACTTCGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036280_2

>merge|NZ_CP036280|2|1445565-1445697|CRISPRCasFinder
ACCTGCTCGACCTCTCGATCCTCGCCAGCAACTTCGACGGCACCGACACCCCGTACGACGTGTCGGACGGCGACTTCAACGGCGACGGTTTCGTCAACCTGCTCGACCTGTCGATCCTCGCCAGCAACTTCGA

>NZ_CP036280|2|2|1445565-1445697|CRISPRCasFinder
ACCTGCTCGACCTCTCGATCCTCGCCAGCAACTTCGA	CGGCACCGACACCCCGTACGACGTGTCGGACGGCGACTTCAACGGCGACGGTTTCGTCA
ACCTGCTCGACCTGTCGATCCTCGCCAGCAACTTCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145445462.1\|1436195_1436846_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145445464.1\|1437718_1438312_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145445460.1\|1434336_1435482_+\|DUF89-family-protein	unknown	unknown	gnl\|CDD\|215489
NZ_CP036280.1\|WP_145445466.1\|1439292_1440582_+\|competence/damage-inducible-protein-A	unknown	unknown	gnl\|CDD\|234789
NZ_CP036280.1\|WP_145445469.1\|1442653_1443604_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|225076
NZ_CP036280.1\|WP_145445472.1\|1447144_1448035_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|223642
NZ_CP036280.1\|WP_145445467.1\|1440636_1441401_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226870
NZ_CP036280.1\|WP_145445479.1\|1457548_1458589_+\|LD-carboxypeptidase	unknown	unknown	gnl\|CDD\|132882
NZ_CP036280.1\|WP_145445480.1\|1458595_1460020_-\|D-alanyl-D-alanine-carboxypeptidase/D-alanyl-D-alanine-endopeptidase	unknown	unknown	gnl\|CDD\|334815
NZ_CP036280.1\|WP_145445478.1\|1454529_1457460_-\|FAD-binding-protein	unknown	unknown	gnl\|CDD\|223354
NZ_CP036280.1\|WP_145445474.1\|1449240_1449861_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145445473.1\|1448041_1449193_-\|DUF2219-family-protein	unknown	unknown	gnl\|CDD\|378338
NZ_CP036280.1\|WP_145445465.1\|1438338_1439235_-\|bifunctional-5,10-methylene-tetrahydrofolate-dehydrogenase/5,10-methylene-tetrahydrofolate-cyclohydrolase	unknown	unknown	gnl\|CDD\|184561
NZ_CP036280.1\|WP_145445477.1\|1453060_1454458_-\|DUF839-domain-containing-protein	unknown	unknown	gnl\|CDD\|225752
NZ_CP036280.1\|WP_145445475.1\|1449884_1450385_+\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|239517
NZ_CP036280.1\|WP_145445471.1\|1445859_1446798_-\|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase	unknown	unknown	gnl\|CDD\|234893
NZ_CP036280.1\|WP_145445476.1\|1450507_1453048_+\|type-II-secretion-system-protein-GspD	unknown	unknown	gnl\|CDD\|224367
NZ_CP036280.1\|WP_145445463.1\|1436864_1437719_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|372917
NZ_CP036280.1\|WP_145445468.1\|1441402_1442416_-\|FkbM-family-methyltransferase	unknown	unknown	gnl\|CDD\|273628
NZ_CP036280.1\|WP_145445461.1\|1435517_1436162_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|225076

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145445471.1\|1445859_1446798_-\|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase	gnl\|CDD\|234893	PRK01045, ispH, 4-hydroxy-3-methylbut-2-enyl diphosphate reductase; Reviewed.	1.11441e-163
NZ_CP036280.1\|WP_145445476.1\|1450507_1453048_+\|type-II-secretion-system-protein-GspD	gnl\|CDD\|224367	COG1450, PulD, Type II secretory pathway, component PulD [Cell motility and secretion / Intracellular trafficking and secretion].	7.06085e-47
NZ_CP036280.1\|WP_145445460.1\|1434336_1435482_+\|DUF89-family-protein	gnl\|CDD\|215489	PLN02902, PLN02902, pantothenate kinase.	6.49003e-71
NZ_CP036280.1\|WP_145445466.1\|1439292_1440582_+\|competence/damage-inducible-protein-A	gnl\|CDD\|234789	PRK00549, PRK00549, competence damage-inducible protein A; Provisional.	3.11289e-140
NZ_CP036280.1\|WP_145445469.1\|1442653_1443604_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|225076	COG2165, PulG, Type II secretory pathway, pseudopilin PulG [Cell motility and secretion / Intracellular trafficking and secretion].	3.52047e-11
NZ_CP036280.1\|WP_145445472.1\|1447144_1448035_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|223642	COG0568, RpoD, DNA-directed RNA polymerase, sigma subunit (sigma70/sigma32) [Transcription].	2.91962e-81
NZ_CP036280.1\|WP_145445467.1\|1440636_1441401_+\|hypothetical-protein	gnl\|CDD\|226870	COG4464, CapC, Capsular polysaccharide biosynthesis protein [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	2.58754e-20
NZ_CP036280.1\|WP_145445479.1\|1457548_1458589_+\|LD-carboxypeptidase	gnl\|CDD\|132882	cd07025, Peptidase_S66, LD-Carboxypeptidase, a serine protease, includes microcin C7 self immunity protein. LD-carboxypeptidase (Muramoyltetrapeptide carboxypeptidase; EC 3.4.17.13; Merops family S66; initially described as Carboxypeptidase II) family also includes the microcin c7 self-immunity protein (MccF) as well as uncharacterized proteins including hypothetical proteins. LD-carboxypeptidase hydrolyzes the amide bond that links the dibasic amino acids to C-terminal D-amino acids. The physiological substrates of LD-carboxypeptidase are tetrapeptide fragments (such as UDP-MurNAc-tetrapeptides) that are produced when bacterial cell walls are degraded; they contain an L-configured residue (L-lysine or meso-diaminopimelic acid residue) as the penultimate residue and D-alanine as the ultimate residue. A possible role of LD-carboxypeptidase is in peptidoglycan recycling whereby the resulting tripeptide (precursor for murein synthesis) can be reconverted into peptidoglycan by attachment of preformed D-Ala-D-Ala dipeptides. Some enzymes possessing LD-carboxypeptidase activity also act as LD-transpeptidase by replacing the terminal D-Ala with another D-amino acid. MccF contributes to self-immunity towards microcin C7 (MccC7), a ribosomally encoded peptide antibiotic that contains a phosphoramidate linkage to adenosine monophosphate at its C-terminus. Its possible biological role is to defend producer cells against exogenous microcin from re-entering after having been exported. It is suggested that MccF is involved in microcin degradation or sequestration in the periplasm.	3.41003e-75
NZ_CP036280.1\|WP_145445480.1\|1458595_1460020_-\|D-alanyl-D-alanine-carboxypeptidase/D-alanyl-D-alanine-endopeptidase	gnl\|CDD\|334815	pfam02113, Peptidase_S13, D-Ala-D-Ala carboxypeptidase 3 (S13) family.	3.73605e-70
NZ_CP036280.1\|WP_145445478.1\|1454529_1457460_-\|FAD-binding-protein	gnl\|CDD\|223354	COG0277, GlcD, FAD/FMN-containing dehydrogenases [Energy production and conversion].	6.57287e-76
NZ_CP036280.1\|WP_145445473.1\|1448041_1449193_-\|DUF2219-family-protein	gnl\|CDD\|378338	pfam09982, DUF2219, Uncharacterized protein conserved in bacteria (DUF2219). This domain, found in various hypothetical bacterial proteins, has no known function.	2.63885e-69
NZ_CP036280.1\|WP_145445465.1\|1438338_1439235_-\|bifunctional-5,10-methylene-tetrahydrofolate-dehydrogenase/5,10-methylene-tetrahydrofolate-cyclohydrolase	gnl\|CDD\|184561	PRK14192, PRK14192, bifunctional methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase FolD.	1.43915e-124
NZ_CP036280.1\|WP_145445477.1\|1453060_1454458_-\|DUF839-domain-containing-protein	gnl\|CDD\|225752	COG3211, PhoX, Predicted phosphatase [General function prediction only].	3.15855e-83
NZ_CP036280.1\|WP_145445475.1\|1449884_1450385_+\|NUDIX-domain-containing-protein	gnl\|CDD\|239517	cd03425, MutT_pyrophosphohydrolase, The MutT pyrophosphohydrolase is a prototypical Nudix hydrolase that catalyzes the hydrolysis of nucleoside and deoxynucleoside triphosphates (NTPs and dNTPs) by substitution at a beta-phosphorus to yield a nucleotide monophosphate (NMP) and inorganic pyrophosphate (PPi). This enzyme requires two divalent cations for activity; one coordinates the phosphoryl groups of the NTP/dNTP substrate, and the other coordinates to the enzyme. It also contains the Nudix motif, a highly conserved 23-residue block (GX5EX7REUXEEXGU, where U = I, L or V), that functions as metal binding and catalytic site. MutT pyrophosphohydrolase is important in preventing errors in DNA replication by hydrolyzing mutagenic nucleotides such as 8-oxo-dGTP (a product of oxidative damage), which can mispair with template adenine during DNA replication, to guanine nucleotides.	6.60357e-40
NZ_CP036280.1\|WP_145445463.1\|1436864_1437719_-\|hypothetical-protein	gnl\|CDD\|372917	pfam14125, DUF4292, Domain of unknown function (DUF4292). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 243 and 287 amino acids in length.	0.00529141
NZ_CP036280.1\|WP_145445468.1\|1441402_1442416_-\|FkbM-family-methyltransferase	gnl\|CDD\|273628	TIGR01444, 2-O-methyltransferase_NoeI, methyltransferase, FkbM family. Members of this family are characterized by two well-conserved short regions separated by a variable in both sequence and length. The first of the two regions is found in a large number of proteins outside this subfamily, a number of which have been characterized as methyltransferases. One member of the present family, FkbM, was shown to be required for a specific methylation in the biosynthesis of the immunosuppressant FK506 in Streptomyces strain MA6548.	1.00372e-24
NZ_CP036280.1\|WP_145445461.1\|1435517_1436162_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|225076	COG2165, PulG, Type II secretory pathway, pseudopilin PulG [Cell motility and secretion / Intracellular trafficking and secretion].	5.75652e-10

>NZ_CP036280.1|WP_145445469.1|1442653_1443604_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MSSMRPVRGFTLIELLVVISIIALLIGILLPALGAARATARGAVCQSNNRNITTALNVYAVDNRGVWPSRGALVDDPDYPEDKRNVGWIPGVSLQGKDSEVLEDGSLFEYLNNVEVLSCPSDDYAEESAGLSYTMNSFIHDIQSNQSLGVTNRPGFEASNGKLYSDANKFRSPSQLIAMVDEGGPNIEYIKVMTGQDVSSLSEAGVNDGYFQWIWSDEPLGNSYGDKTKWYHQGSAAFGFADGHGELRSKTDPEVINFRGHSFKFKVGASGSRTFGFGKLWDPLGEAPLDIYDAEPASGGGDGGDGGDDGGRPSRP
>NZ_CP036280.1|WP_145445468.1|1441402_1442416_-|FkbM-family-methyltransferase
MPARLFVVSARLRYALDRSRDRYPRDEPPGASMAGWYLPLYNLVRSSGPLRSVARAIRYAMPDSKVTTRVDYLGPFQFRLKRHHWLYGSRALSGHARNLAMFERVIDPDAVFYDVGLNIGYYARFIASHFPVRRVAGFEPMTQNIDLARRNIELCPRADVIRLHEIALGDTDGDELLQVDDITDGSAVLDRVSGGQPAEGRLNAGLPGMTESVRMMRLDTFVAEALEPPPTAMKIDTEGAEVIVLRGARETLETHAPHLVIATHGREPAEGCFRLLDPLGYGLYGWVPSGQRGGSYRRLTFENMAELADNNILASRNHARLEPEVTPLPMDDLSLQG
>NZ_CP036280.1|WP_145445467.1|1440636_1441401_+|hypothetical-protein
MSDATPTPTTEPPLPATGRLDLHAHLIPDVDDGSRSYDETVALVQRLKRADYSGSVCTPHVWPELFPDNTPAKIADLTAGLRGHLADNGIDYTLWDGGELRLFEGVTAWLKANGVPTLGPSRAVLCDFWEAEWPTFVDEAFEWMLSEGYQPLLAHPERIPMTEGLEAELDRVQALGVMLQGNLRCLTDEESPLSRLRARAYLQDGRYSVMALDVHRADSLDSRIDGLGLGAELVGAELIDELTMAAPRKLLQIA
>NZ_CP036280.1|WP_145445466.1|1439292_1440582_+|competence/damage-inducible-protein-A
MFDAAIVAIGDELVLGQTVDTNTAWVCQRLASRGIMAKLHLTVPDDRAMIRDAFAQGARTAPWVIVTGGLGPTEDDLTRFAFADALGVELAEDPQAMAHLQTWYAGRGKTMPQTNLVQAMLPAGTTVLPNPVGTAVGMQGSLGGSRVFVMPGVPRELHAIFEESVQPLIDAATAGHFLLTRKINTFGLGESTVAGVLGDLMRRDANPTIGTTVSGGVVSIRLRAETEDRAQAEAMLDDAEAAVRERMGAFVFGVDSELLQEAAVRLLGDKSITVATAESCTGGKVAAALTDVAGSSAVYPGGWVTYANEQKAANLGVDAALIEAEGAVSHAVACAMAEGARREAGVDLAISTTGIAGPSGGTDTKPVGTVWFGLADVGGSRAWHAHLRGNRTMVRDRARMIALQIVRFAALGDDPAGIEWLSEAVPEGV
>NZ_CP036280.1|WP_145445465.1|1438338_1439235_-|bifunctional-5,10-methylene-tetrahydrofolate-dehydrogenase/5,10-methylene-tetrahydrofolate-cyclohydrolase
MNEQADAPVILKGKPVADLILENCRQRVRQIVDATGVQPCLATVLTGSDPASQKYVDRKAKLCQDLGMKSIKVTFPETTTTEELVAKTRELAEDPAVHGILLQHPMPGQIDERAAFEAIGPAKDVDGVTFYSFGTMTYGLAGFDSATPGGIMRLIRHYKVPVEGRHAVVIGRSVILGKPMAMLLLDANATVTICHSRTTNLPEVVRQADIVVAAVGKPNFVKGDWIKPGAVILDAGFNPGPKGNVGDVDYDDCLPRSGMITPVPGGVGPMTLAVLMEQTVTGAARQLGVETAREPAAV
>NZ_CP036280.1|WP_145445464.1|1437718_1438312_-|hypothetical-protein
MSSLNASAYELPRATGSCASTGRAFEPGEPYFAALVETETSAEPSSKPAAPSLGFARVDVSAEAWDSGYRPERLFSFWKTTQPEPNAKKSPWADDSVLLDLLERLADTEDRKRLALRHVITLVLMRKKLLRYDGAEKHDEGDETRTVWQLTPKLDPAKGPLGKWNEDRQISVLDPGLTEDDVALLIEQLGQIVEIDD
>NZ_CP036280.1|WP_145445463.1|1436864_1437719_-|hypothetical-protein
MQRFLVLALILAAALFAGCKSRPVEVVPFGLPVPLEDAPPPPSYALAASMHNERIANIDRLWAATDLKLEWIEDEEHKIEQGSGNLLLIRPDQIALTIGKLGHVRLWAGMNPTADYLFDLRGDGVVYIHRRPDGRPADIFSPDLPVPLQPRDVPWLLGIMPLPETGNIEVVNGYWLLEPEGVPTRLLLNPHDLTPFRIDRIGPDGTSSILAIHSNFLPVDGIPGPTTLMARRLQIVENGKEARIDLDLDRLRGGQQAQRKLRPAAFDLDRLIKSHEPGEVVELQ
>NZ_CP036280.1|WP_145445462.1|1436195_1436846_+|hypothetical-protein
MNLHVLLADERLRKYGIPTGAALLAILSLCVGSYLWWSMQMPAMPETPDDVRAMLEDSRLRHLSPDRREAYAQKAFAIVSSMEGDQRGELFGALRENQMARDNMRMMMQQMMVDRARAYALADEAEREQILADSVERMRAMRPPGGGRPEGGRPEGNRGGGGDRQSRFMDRAATGNPQHGQMMREFFQAMREYREKNNIEGGRGGGAGRGDLNKPA
>NZ_CP036280.1|WP_145445461.1|1435517_1436162_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MGRLGVGVLMQDMRRISLGFTLIELLVVISIISILIGILLPSLAAARNAARSVGCLSNLRQIGIGVELYLDANQRVYPRVRTMPSPFPTALDDPVPPYIGVKLDPYLQGLYDPDADRGIYICPADTQVAELCGASYGFESALNHRTLEDSPLVRRFRLSPSQIWVLQDYDGWPFVLEDGSEIEVDFFHWRRNAYHADGHASAMESSGDNPFTPD
>NZ_CP036280.1|WP_145445460.1|1434336_1435482_+|DUF89-family-protein
MDLAEENPCFYVGTDDHADPLREHAVFPLLADPQSYVAGTWDMRHNHEQRTYWLGLFRSHFPLLMAEARRERADAGADTEAVECALNKAQSDFMAYVDACEADPDGIERLDILSLCWARERALRAVGIADPYRLAKAEHTESALGFLTAWLEELDAMPRAEKWESLLRGVLAGNLFDLGATKTVHLYQEGGQAPTFHDTLSKLKPRPWFCDDADAFLAEWPGRMFNKALLFIDNAGPDVVLGMLPLARELARYGRVVVVANGAPSLNDVTISELDALLERVSAMDPTVAEQVRTGRMTTVSSGNWAPLIDLTLISPELAAEASDGVDLVVLEGMGRAIETNLEAKLTCDVLKMAMIKDEGVASAKGAGLFDLVCRFESAES
>NZ_CP036280.1|WP_145445471.1|1445859_1446798_-|4-hydroxy-3-methylbut-2-enyl-diphosphate-reductase
MKIMLANPRGFCAGVNMAIQTVDEALKIVGTPLYVYHEIVHNRHVVARFEEQGVVFVDHIDDVPSNSTVIFSAHGVSPEVRNAAKSRGCTMIDATCPLVTKVHMEAVRYARQGFRIILVGHAGHDEVVGTVGEAPDAITIVESAADVERLQISDDVPLVYLTQTTLSMDDAQIIISALEDKFPQIKSPPSEDICYATTNRQHAVRDLATEADLVLVVGSKNSSNSVRLTEISENIGTRAYLMDDVTELRDAWFEGVNSVLVTAGASAPEDLVQEIVHHLEKTYGGKTEDRLVVEEEMHFNLPVTLRVMKQNA
>NZ_CP036280.1|WP_145445472.1|1447144_1448035_+|sigma-70-family-RNA-polymerase-sigma-factor
MGNRALKSGLEIYLSQIDESPLLTADQEKELARRIIEKNCPEAREHMIRSNLRLVVAIAKRYMNRGLPLVDLIEEGNIGLMRAVEGFDPDQGARFSTYGCWWIKQSIKRALINAVQPIHIPAYMVELIAKWKRASRELEEKLGRQPTIAELSKEMDLPAKKIRIISKAVRASQRPQRGGSGEDDQAPTLSEMLADDKVMAPDEQATVEDDLKTIRQLLDAIDDREAKILRLRYGLDGTEPMTLKDIGVEIGLTRERVRQIEIEALRKLQRRLESDRPLAAVRARASVEEDRKRQSA
>NZ_CP036280.1|WP_145445473.1|1448041_1449193_-|DUF2219-family-protein
MHRLSRTTRAVRRPVSGLPQPSGIFLDVTHALLFGCAMIFLSAVPLRAQPVSDPVPAEPQGYLSVSFLMENDSTPLKIIDRSDRQYTNGLGLLITHQPDWADALAVHIPSLDHLDTPDDTAVGYLLAQKIFTPDNLDNPAVDPDDRRYAGYTYLGAFLQRANQHTLDHFQLDLGWIGPSSGADVVQSNWHDAINIQEPMGWGQQLPDEPTIQATFRKKWRVDLDRSPDGFQHELIPRAELILGTVQRQAAADLLWRASWLPLPRDFGPSQLDDPDAPMIGLTDHPDSFRIVSEPRWTAYFYGRAGIVLVEHDTFIEGSSTQSDTGLDAKPLVGRFQVGIEAARHTGNGTFRIGLYQTILTDQFEGQTRPHSFGGLAISYAWRF
>NZ_CP036280.1|WP_145445474.1|1449240_1449861_-|hypothetical-protein
MLSLPQIQRHLLDRDYDQLLIDLVRNGTLLPMPLRLRLSQSPGGCLGLALRRVVELTHGPTHLGNTIFDGLLAECVTDHDPIVLAACLSGIERARALGAVGPDQADALEQCANRLWFALAQRQQHTGLLGAEPDRTETDLALTSAFVVYLLAPVSSRAHHLDLSGLLTALEDRRPLDDRAAEELVQVALASWPRATPVARPLIQAA
>NZ_CP036280.1|WP_145445475.1|1449884_1450385_+|NUDIX-domain-containing-protein
MHEQYPNEFRVSSVCSDIFRHARDRVSWVLLEVLSMARLIEVGLGVVIDSERVLVTQRKPDGPLPGLWEIPGGKVERGETHEVCVRRELMEEVGLEVSVGAIIGVWEHAYPHGAVRLWAYWCRRLSGEARAIEVADLTWADRLSLHERSYPEASLPLISEIASALP
>NZ_CP036280.1|WP_145445476.1|1450507_1453048_+|type-II-secretion-system-protein-GspD
MAKDGAGTEFCLTARLGLVLVLLVTGLCRGQAALSLENAGLYLPQQDMTVEVAEEVLEVVRSRAIASLGYQIIPDPGVLLPGGPPGLRGTTYLRRRTSQGEHYIQMGYKLFDHQPLHLWVYGQIVTEKGVTANGDLAGMEKMIEDAIKNVEAFYKSFRPGDLATGVIDLSYIEADRCMAILKGLGYQTINFKEAGNGVGGAKLIEPATPIDVRDLPVVMALPAAAHTGLVGAGSAQSSGGQFKLSLVPSIAGSFENYTSATPLMQLMVLYDAEEAHVFTSLVKKIRDTIDVPARQLVIEAMILEISETGLDKLGVQWELSNVPKDSIESFAFGRLPDFGTGQGPTFDLTLIDIGNNWRVKVQALVRDGDAEILSRPSVLTLDHRQASIRIGEDIPIATSIRGATGGDTIQFSFAYIPVGILLNVRPRISSNGQEVTMQVDGVVSNEVPGGDLVVVDQDGNELGSAPRVSSRRVQTHTRIANNTPFIIGGLISNETSTTQDKVPLLGDIPWLGAAFRSSDTEVIKREVIIVITPYVLPTEGIPGRVLPEDKDVFDSFDNQLFGDVYRIRAEDVPDLAFLDDNPELELARNRAETITSRFPNLINQYPFNQFLDGRVPGEEVLVYHLMYEVIERREIEKSIQARRLVFLKPRDDRPAGASVSFLIQHIGQELGVEIPKHSIGFKWLFNQMQGHALALTYTIPSEPKVDEVLFKAIPEVRLVPCADRDEWLNLLYELNRPGDGGEKRHTILIRNEEDLKRLMRCVVLRHAVELNQGQDQLRLKDYQRGRQLIMPETSRDETFLIDHEVAEYYYLSVQYFAAMLDRIRADSEALRQEIDSIESGSVLGGR
>NZ_CP036280.1|WP_145445477.1|1453060_1454458_-|DUF839-domain-containing-protein
MSIARRDFVKSAAAVSLGFIGLDLFCRSATPVLAAAPNNAGYGPLIDDPEGILALPEGFSYRIISRLGEEMDDGLLVPGMHDGMAAFPADGGKTVIVRNHEQVNTQTGTSPFGPNAERLGKIDRDLIYDAQSPCLGGTTNIVYDTRTGQVEKHFLSLAGTVRNCAGGPTPWNTWITCEETVAPKGDGYDLAHGYNFEVPATTTPGLVRPVALKAMGRMNHEAIAVDPVSGIVYQTEDRGDGLIYRFIPNEPGRMEKGGRLQALVLTDHPSADTFNYRNRDGSARGLNIPVRETLNVSWVDIENPEAPKDDLRFQGYGKGAARFARGEGMWYGNDSIFFACTSGGSKRGGQVFRYVPSRFEGKPEERRFPGRLELYIEPDDRGVLDMADNLTVAPWGDVILCEDGSDKQFVVGVSPDGQVFKVAGNQLSTSEFAGACFSPDGSTMFVNIQKQGLTFAITGPWQRRA
>NZ_CP036280.1|WP_145445478.1|1454529_1457460_-|FAD-binding-protein
MIQPTATHTFDLPAIERDLTEAVRGEIRTDIFSRGIHATDASHYQIMPTCVVNPRDEADCVAAVKVAAKHSLPMTARGAGTSLSGQTHGVGMIIDVSQHMDKLIEVNEEERWARVQPGIVRDRLNAQLRHLGLHYAPDPATGSRATVGGIIGNNSSGTRSILYGKAQENLLACRVLLADGTLLDLDACDWDRWCAKSNQENLEGRIYSRFGQIIAENRDEIEARFPKVMRRVGGYNLDAFLDDPGQTPWNLSNIIVGSEGTLGILIEAKVKLVENPKATALCVVHFDELLPSLRCLPAMLEHGPSAVELLDHYVIDEAIRNPATKHLCHFMEGHPKAVQIVEFYGDDQAHAASRAEAFAESMRQQGVGFAQAVRRDPKEISEAWDVRKLGLGLIANTPGPRKALDFVDDACIPIEHLAEYVERLLKVCEEHGTSAAVYAHASVGVLHIKPLIDLHYKEEQEKMRSIAWAAFEMCKEYGGSWSGEHGDGLVRGEFVRPFFGDQLYEAFKQVRALFDPRGLMNPNKILDTPLMTEHLRYGDAYRLDVIDATESRINYHYRDQGGFASAVEQCSGVGACRKVDVGTMCPSYMATRDEEASTRGRANALRMAMSGQLGPDAMTDKRMKDVLGLCLACKSCKTECPNSVDMAKMKSDVLQMMHDRFGLPLGYRLMGDSPTIARLVCGPLAPIVNWVQGLTPMKKLLEAIAGIDARRPAPKFATWSLQGWFRRHRKPKDDRPEVVLFDDTYASYFEPHVGVSAVELLEGCGYKVTLARAGCCQRPRLSKGMVRAAKKAGEKTLRNLDKYAREGLPIVCLEPSCASSLADDLPDLIDDVELGKRVAPQVMMIDEFLAAEAKAGRINATIKARFDKLMIHGHCHQKSLNSTQGMKDVLDLAENVTYHEVDSGCCGMAGSFGYEEFEVSKQVYDLRLGPAIEKLEPGEEVVACGFSCRHQLSDFSGLKAYHWVEVVSAENSNEPR
>NZ_CP036280.1|WP_145445479.1|1457548_1458589_+|LD-carboxypeptidase
MKSTSKRSRVRVVAPSSTVPQVELDMGLKRLADAGFAAEVADQVRETWYLHAGTDGARAQAIYDAGRDPHVDILWCARGGYGAAKLLPLLDELTEKHGAPDPKLLIGYSDITILNHYTRLKWGWGTMHANMPATLSFNSMAESEFDTTMKWARGELCEPAWSGQTFEYLACPPSEPVRGEVVGGNVSVWNSLYGTPWSPGSITGKILFFEDLNEYHYRLDGLVTHLLQAGGLDGVAGIVLGDFTNCDDEAGTCLAAPVEGEERSLLLKEGLDALPAERAQPLRPQVPQRDALEHMLVAPARDRGIPVMKGLPVGHGPGFAPLPLGSVFEMTPEGAFNLVSWDWLSE
>NZ_CP036280.1|WP_145445480.1|1458595_1460020_-|D-alanyl-D-alanine-carboxypeptidase/D-alanyl-D-alanine-endopeptidase
MTLTRATPLRWLLIALLVFLTAAPVGADLADLGRQIETTINRIDQQGILAAARVVDLRTGEVIFEQNETTAVKPASNLKLFITAAALDKLGPEVTFDTHLYLDGDDLIVVGSGDPAFGDLSTMQRQGKTMLATFDAWAAVLKDRGVTRIAGDLMYDDTALGDEWLCPSWPASNLLHWYGAPSSGLNLNNNCIDILIEPIDNNMGRVSYIPDAEMITVHNRTGGDKPLSVVKVAGKHEYIVSGKITRRRTFYKPVDDPGLFFAQALKAHLARLGIVVEGEIRRLESRRKLRLTDPPLAVHSSAMEDVLRRINSNSQNMMADSLIRIAFATRNTNYRSAGNALLTYARERGFQALEPMRIVDGSGLSHDNRVSTKALSELLTRMSHHKDFDHYYASLSVAGESGSLRNRMKEAEGNIRGKTGSISGVRSSSGYIDTPDGRRIVYAFVFNNLVGANHTRAIETMDATCMLIYGWEQW

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Crispr_ID: NZ_CP036280_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_3

1597973-1598113

Orphan

Consensus_repeat	Method
CCGGCGAGGATGGAGAGGTCGAGGAGGTCGACCGCGCCGTCGCTGTTGATGTCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036280_3

>merge|NZ_CP036280|3|1597973-1598113|CRISPRCasFinder
CCGGCGAGGATGGAGAGGTCGAGGAGGTCGACCGCGCCGTCGCTGTTGATGTCGGCGGTGGTCTGTGTTGCGCTCGCGCCGAAGTGACCGGCGAGGATGGAGAGGTCGAGGAGGTCGACCGCGCCGTCGCTGTTGATGTCG

>NZ_CP036280|3|3|1597973-1598113|CRISPRCasFinder
CCGGCGAGGATGGAGAGGTCGAGGAGGTCGACCGCGCCGTCGCTGTTGATGTCG	GCGGTGGTCTGTGTTGCGCTCGCGCCGAAGTGA
CCGGCGAGGATGGAGAGGTCGAGGAGGTCGACCGCGCCGTCGCTGTTGATGTCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145445583.1\|1583130_1584171_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|349766
NZ_CP036280.1\|WP_145445595.1\|1613103_1614402_-\|TRAP-transporter-large-permease-subunit	unknown	unknown	gnl\|CDD\|224509
NZ_CP036280.1\|WP_145445581.1\|1580496_1581675_-\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|271213
NZ_CP036280.1\|WP_145445590.1\|1603793_1605782_-\|sodium:solute-symporter	unknown	unknown	gnl\|CDD\|271371
NZ_CP036280.1\|WP_145445593.1\|1609377_1612263_-\|DUF4861-family-protein	unknown	unknown	gnl\|CDD\|379779
NZ_CP036280.1\|WP_145445585.1\|1585488_1586118_-\|cobalamin-binding-protein	unknown	unknown	gnl\|CDD\|239021
NZ_CP036280.1\|WP_145445598.1\|1615952_1616798_-\|5-dehydro-4-deoxy-D-glucuronate-isomerase	unknown	unknown	gnl\|CDD\|179169
NZ_CP036280.1\|WP_145445586.1\|1586352_1587117_+\|DUF1638-domain-containing-protein	unknown	unknown	gnl\|CDD\|377918
NZ_CP036280.1\|WP_145445580.1\|1579149_1580418_+\|amidohydrolase-family-protein	unknown	unknown	gnl\|CDD\|368185
NZ_CP036280.1\|WP_145445596.1\|1614398_1614875_-\|TRAP-transporter-small-permease-subunit	unknown	unknown	gnl\|CDD\|225632
NZ_CP036280.1\|WP_145445584.1\|1584073_1585468_-\|uroporphyrinogen-decarboxylase	unknown	unknown	gnl\|CDD\|239548
NZ_CP036280.1\|WP_145445579.1\|1578598_1579150_+\|D-lyxose/D-mannose-family-sugar-isomerase	unknown	unknown	gnl\|CDD\|380442
NZ_CP036280.1\|WP_145445597.1\|1614864_1615896_-\|DctP-family-TRAP-transporter-solute-binding-subunit	unknown	unknown	gnl\|CDD\|270389
NZ_CP036280.1\|WP_145445588.1\|1588690_1589356_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|225024
NZ_CP036280.1\|WP_145445591.1\|1605847_1607467_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|374201
NZ_CP036280.1\|WP_145445594.1\|1612303_1613074_-\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|188170
NZ_CP036280.1\|WP_145445599.1\|1616856_1617630_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|224332
NZ_CP036280.1\|WP_145445587.1\|1587113_1588694_+\|DUF4445-domain-containing-protein	unknown	unknown	gnl\|CDD\|379651
NZ_CP036280.1\|WP_145445582.1\|1582016_1583117_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|239548
NZ_CP036280.1\|WP_145445592.1\|1607400_1609347_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145445583.1\|1583130_1584171_-\|hypothetical-protein	gnl\|CDD\|349766	cd03112, CobW-like, cobalamin synthesis protein CobW. The function of this protein family is unknown. The amino acid sequence of YjiA protein in E. coli contains several conserved motifs that characterize it as a P-loop GTPase. YijA gene is among the genes significantly induced in response to DNA-damage caused by mitomycin. YijA gene is a homologue of the CobW gene which encodes the cobalamin synthesis protein/P47K.	6.5762e-38
NZ_CP036280.1\|WP_145445595.1\|1613103_1614402_-\|TRAP-transporter-large-permease-subunit	gnl\|CDD\|224509	COG1593, DctQ, TRAP-type C4-dicarboxylate transport system, large permease component [Carbohydrate transport and metabolism].	1.09933e-108
NZ_CP036280.1\|WP_145445581.1\|1580496_1581675_-\|PEP-CTERM-sorting-domain-containing-protein	gnl\|CDD\|271213	cd14254, Dockerin_II, Type II dockerin repeat domain. Bacterial cohesin domains bind to a complementary protein domain named dockerin, and this interaction is required for the formation of the cellulosome, a cellulose-degrading complex. The cellulosome consists of scaffoldin, a noncatalytic scaffolding polypeptide, that comprises repeating cohesion modules and a single carbohydrate-binding module (CBM). Specific calcium-dependent interactions between cohesins and dockerins appear to be essential for cellulosome assembly. This subfamily represents type II dockerins, which are responsible for mediating attachment of the cellulosome complex to the bacterial cell wall.	2.9581e-06
NZ_CP036280.1\|WP_145445590.1\|1603793_1605782_-\|sodium:solute-symporter	gnl\|CDD\|271371	cd11477, SLC5sbd_u1, Uncharacterized bacterial solute carrier 5 subfamily; putative solute-binding domain. SLC5 (also called the sodium/glucose cotransporter family or solute sodium symporter family) is a family of proteins that co-transports Na+ with sugars, amino acids, inorganic ions or vitamins. Prokaryotic members of this family include Vibrio parahaemolyticus glucose/galactose (vSGLT), and Escherichia coli proline (PutP) and pantothenate (PutF) cotransporters. One member of the SLC5 family, human SGLT3, has been characterized as a glucose sensor and not a transporter. This subfamily belongs to the solute carrier 5 (SLC5) transporter family.	7.59629e-85
NZ_CP036280.1\|WP_145445593.1\|1609377_1612263_-\|DUF4861-family-protein	gnl\|CDD\|379779	pfam16153, DUF4861, Domain of unknown function (DUF4861). This family consists of uncharacterized proteins around 400 residues in length and is mainly found in various Bacteroides species. The function of this family is unknown. However, in many instances the domain lies upstream of a glycosyl hydrolase family, usually family 88, so it might be involved in carbohydrate binding.	9.48904e-85
NZ_CP036280.1\|WP_145445585.1\|1585488_1586118_-\|cobalamin-binding-protein	gnl\|CDD\|239021	cd02070, corrinoid_protein_B12-BD, B12 binding domain of corrinoid proteins. A family of small methanogenic corrinoid proteins that bind methyl-Co(III) 5-hydroxybenzimidazolylcobamide as a cofactor. They play a role on the methanogenesis from trimethylamine, dimethylamine or monomethylamine, which is initiated by a series of corrinoid-dependent methyltransferases.	1.44445e-74
NZ_CP036280.1\|WP_145445598.1\|1615952_1616798_-\|5-dehydro-4-deoxy-D-glucuronate-isomerase	gnl\|CDD\|179169	PRK00924, PRK00924, 5-keto-4-deoxyuronate isomerase; Provisional.	1.01377e-160
NZ_CP036280.1\|WP_145445586.1\|1586352_1587117_+\|DUF1638-domain-containing-protein	gnl\|CDD\|377918	pfam07796, DUF1638, Protein of unknown function (DUF1638). This family contains sequences covering an approximately 270 amino acid stretch of a group of hypothetical proteins. These proteins are expressed by archaeal species of the Methanosarcina genus.	3.00496e-50
NZ_CP036280.1\|WP_145445580.1\|1579149_1580418_+\|amidohydrolase-family-protein	gnl\|CDD\|368185	pfam04909, Amidohydro_2, Amidohydrolase. These proteins are amidohydrolases that are related to pfam01979.	1.7964e-09
NZ_CP036280.1\|WP_145445599.1\|1616856_1617630_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	3.49723e-66
NZ_CP036280.1\|WP_145445584.1\|1584073_1585468_-\|uroporphyrinogen-decarboxylase	gnl\|CDD\|239548	cd03465, URO-D_like, The URO-D _like protein superfamily includes bacterial and eukaryotic uroporphyrinogen decarboxylases (URO-D), coenzyme M methyltransferases and other putative bacterial methyltransferases. Uroporphyrinogen decarboxylase (URO-D) decarboxylates the four acetate side chains of uroporphyrinogen III (uro-III) to create coproporphyrinogen III, an important branching point of the tetrapyrrole biosynthetic pathway. The methyltransferases represented here are important for ability of methanogenic organisms to use other compounds than carbon dioxide for reduction to methane.	2.05996e-61
NZ_CP036280.1\|WP_145445579.1\|1578598_1579150_+\|D-lyxose/D-mannose-family-sugar-isomerase	gnl\|CDD\|380442	cd20308, cupin_YdaE, D-lyxose isomerase YdaE, cupin domain. This family includes D-lyxose isomerase (D-LI; EC 5.3.1.15) homologous to YdaE from the sigma B regulon of Bacillus subtilis, a protein with an active site that is highly similar to the E. coli O157 z5688 D-lyxose isomerase. YdaE may have a synergistic role with ydaD, an NAD(P)-dependent alcohol dehydrogenase, in the adaptation to environment stresses; YdaD may be active against the ketose sugar produced by YdaE and function in providing resistance to oxidative stress through the production of reducing equivalents in the form of NAD(P)H. YdaE forms a cupin-type beta-barrel, with two alpha helices at the N-terminus. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	1.26043e-93
NZ_CP036280.1\|WP_145445597.1\|1614864_1615896_-\|DctP-family-TRAP-transporter-solute-binding-subunit	gnl\|CDD\|270389	cd13671, PBP2_TRAP_SBP_like_3, Uncharacterized substrate-binding protein of the Tripartite ATP-independent Periplasmic transporter family; the type 2 periplasmic-binding protein fold. This subfamily includes uncharacterized periplasmic substrate-binding proteins similar to TRAP transport systems such as SiaP (a sialic acid binding virulence factor) and TeaA (an ectoine binding protein). TRAP transporters are a large family of solute transporters ubiquitously found in bacteria and archaea. They are comprised of a periplasmic substrate-binding protein (SBP) and two unequally sized integral membrane components: a large transmembrane subunit involved in the translocation process and a smaller membrane of unknown function. The driving force of TRAP transporters is provided by electrochemical ion gradients (either protons or sodium ions) across the cytoplasmic membrane, rather than ATP hydrolysis. This substrate-binding domain belongs to the type 2 periplasmic binding fold protein superfamily (PBP2). The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	7.56565e-117
NZ_CP036280.1\|WP_145445588.1\|1588690_1589356_-\|hypothetical-protein	gnl\|CDD\|225024	COG2113, ProX, ABC-type proline/glycine betaine transport systems, periplasmic components [Amino acid transport and metabolism].	0.00153411
NZ_CP036280.1\|WP_145445591.1\|1605847_1607467_-\|hypothetical-protein	gnl\|CDD\|374201	pfam15892, BNR_4, BNR repeat-containing family member. BNR_4 is a family which carries the unique sequence motif SxDxGxTW which is so characteristic of the repeats of the BNR family, pfam02012. It is unclear whether or not this unit is repeated throughout the sequences of this family, but if it is then the family is likely to be bacterial neuraminidase.	6.13162e-09
NZ_CP036280.1\|WP_145445596.1\|1614398_1614875_-\|TRAP-transporter-small-permease-subunit	gnl\|CDD\|225632	COG3090, DctM, TRAP-type C4-dicarboxylate transport system, small permease component [Carbohydrate transport and metabolism].	4.80822e-34
NZ_CP036280.1\|WP_145445587.1\|1587113_1588694_+\|DUF4445-domain-containing-protein	gnl\|CDD\|379651	pfam14574, DUF4445, Domain of unknown function (DUF4445). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and archaea. Proteins in this family are typically between 525 and 664 amino acids in length. The family is found in association with pfam00111.	1.17616e-77
NZ_CP036280.1\|WP_145445582.1\|1582016_1583117_-\|hypothetical-protein	gnl\|CDD\|239548	cd03465, URO-D_like, The URO-D _like protein superfamily includes bacterial and eukaryotic uroporphyrinogen decarboxylases (URO-D), coenzyme M methyltransferases and other putative bacterial methyltransferases. Uroporphyrinogen decarboxylase (URO-D) decarboxylates the four acetate side chains of uroporphyrinogen III (uro-III) to create coproporphyrinogen III, an important branching point of the tetrapyrrole biosynthetic pathway. The methyltransferases represented here are important for ability of methanogenic organisms to use other compounds than carbon dioxide for reduction to methane.	3.06248e-18
NZ_CP036280.1\|WP_145445594.1\|1612303_1613074_-\|SDR-family-oxidoreductase	gnl\|CDD\|188170	TIGR01832, 2-dehydro-3-deoxy-D-gluconate_5-dehydrogenase, 2-deoxy-D-gluconate 3-dehydrogenase. This model describes 2-deoxy-D-gluconate 3-dehydrogenase (also called 2-keto-3-deoxygluconate oxidoreductase), a member of the family of short-chain-alcohol dehydrogenases (pfam00106). This protein has been characterized in Erwinia chrysanthemi as an enzyme of pectin degradation. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	1.25025e-108

>NZ_CP036280.1|WP_145445588.1|1588690_1589356_-|hypothetical-protein
MRTHNILCSTLILAALALASASTTAHAGVFRFVAAEPAYEVLVGETVIVDLFLQEDIPDLAISTLIAENGLISLDVRVDATSADTDPATMTAFNTNDLDFNDPLGPIVTLTPDQLRTVLFQDPFEPLGVLGTETPQPIGARRDVYIGSLIIQAGNLEDQTTIFTLADDLLVGEFTLTLDGIAALDTTIEPGTFTVTTIIPEPLSIGIFTLGLAALTRRCLH
>NZ_CP036280.1|WP_145445587.1|1587113_1588694_+|DUF4445-domain-containing-protein
MSEGCRLRVVAEGVDDVVIDVGRDALGESVAEILYGAGLGLNTRCGRRGVCDGCFVEELGRERVERRRACAWRLEAGEAVIRIPRRSRASHRPQVLEHFDLRVPYAHDPLADEGVGIAVDLGTTTVAVVVVDLADGRVLARRSRFNGQIELGDDVLSRINLCGRGAGQLVLLQKAVVAGTLRPLILEALGEAGVELRDLGCVTVAGNTTMLHLLVGEDPTPMGAVPFTPGFVEHRVVTAGELGLALPGCGDLPVHLLPSVSAYVGADVLGGVLSTGLAYEAGASLLVDVGTNGEMVLVHEGKMTACATAAGPAFEGSGLSHGMRAARGAIERVDLEREPFGVACGTIGDAEAEGLCGTAYLDLLAQGRAVGLFNERGRFADPLPAGAESWMVDHEGVRGLAVAEGVVVTEVDVALLLQAKGAIAAGILTLLELAGVSACDVGRVYLAGGFGMSLRVEHAIAMGLLPGFRVDQVSLAGNSSLASAYLALVDRSSLEELERLRGEVESIELNQVASFEDHYIDCLSLG
>NZ_CP036280.1|WP_145445586.1|1586352_1587117_+|DUF1638-domain-containing-protein
MDGKMRHEVAAPGGVWVITCAVLELEVEAMLRDRADVVGVTRLPQGLHNEPDRLREELQLRIDEAETCAGCGVIVLVYGLCSRGTEGLRTRRCRLVIPRAHDCITLLLGSKERYAAYVSEHPGTYWYSPGWNAHHVPPGPKRYELLRREYVEKYGEDNADFLMEMEQGWFKEYNRATYVHLSIGATDEDRAETRRCADWLEWTYDEVAGDPGLMEALLSGAWDEERFLVLEPGEAFVMTADERVIERVKGEASS
>NZ_CP036280.1|WP_145445585.1|1585488_1586118_-|cobalamin-binding-protein
MSALNDLTEAIKKGDRKLATASTETELAAGTSPNTILEALIEGMDDVGQRFKANQIFVPEVLIAARAMKEAMAILEPKLVEAGYKPLATAVVGTVEGDLHDIGKNLVVMMLKGASFQVIDLGTNVSPEKFVEAVKESGATVVGLSALLTTTMPAMKKTIDAINEARLEGVSVIIGGAPVTQAFADEVGANGFAPDAASAVDTVRTLINA
>NZ_CP036280.1|WP_145445584.1|1584073_1585468_-|uroporphyrinogen-decarboxylase
MTGKQIILDAIAGKNTPRPAWLPFVGVHGGKLIDQTATDYLKSADNIVKGLTKAVELYRPDGLPIAFDLQLEAEVLGCQLNWADKTPPSVTSHPMSAMEGPGASLEDLPAFSTDAGRFPIVWEATRRMRHTFGDQLALYGLLTGPFTLTSHLMGTDLFLQMFDDEELVLKTMAHCTDIAKQVASRYLENGADIIAVVDPMTSQISPEHFEQFVAPSLNDLFSHIREKGGLSSLFVCGDATRNLEVMAATACDNVSIDEQIDLNTIRELTVPNNKSFGGNLKLTVVLLMGDTDDAKRDAIHCIDTAGDSGFILAPGCDLPYDVKPENLQAVAELVHDPYQRDVARTLADKDADDFADIQLPDYNDPAQVTVDVITLDSASCAPCQYMFAAATDARSRFPEDTPVVIREHKITTRQGVGMMSRLNVGALPSICIDGELAFASVIPDTKTLADRIARRLDEKQTANA
>NZ_CP036280.1|WP_145445583.1|1583130_1584171_-|hypothetical-protein
MANSPSPPSSPTPRHSPTGSHDVSTRNRPPTPERRMTDQGTIPLTLVTGFLGSGKTTFLRAIARKHAERRLAYVVNEFSQHDIDGRLLADAPNAVTVPGGSIFCTCLVTRFREVMNTLAHTHNSSPLEGVIVEASGIADPSVAQRMLHETQLDRHFNLAHTICLVAPDKLNTLLKTLPNTRAQIAASHTAIITMIDQHPADQIDQTHALLHEINPSLDIRRASFGNTDINPFQKPDTTHTSVEGEYATCADTNYERWIIHVNPARSRDELNAFLNTLRNHIYRAKGFVLLDNQHLFVDIAADRVRWKPANTENPDSQLVIIGPASQRDAVQTLLLQNKHLLSANAA
>NZ_CP036280.1|WP_145445582.1|1582016_1583117_-|hypothetical-protein
MRPDINHEPDFNRFLDTLLLRKAWTRPPQFDFHIDITHRSEILGRPCVSPADEVEVFRLCGYDYVQAKLYPPMTELYEHQDRQRLAAGADTHSGAGVMPDYDTYKARRWSWHDMAEGKLDAISDTLDFIEQMAEATPPNTKLLVHIADIFTFSWEMIGFDAFCFASIEQPEWIEDVMGSLAAAIENAFQAILERVGDRAGAVLYSDDIAYTEGLMLSPDFFRENLFPHIARLINRAKARNLPLIYHSDGKLYDVFDDLAAIGVKGIQPLEPKSMDPLEIQKGWPGRFCLLGNIDLDLMARGTPDQVEAAVRNRIDTLNTHGGYIPGISNTVPDYVRIENYCRMIETIKSYPDEPIPENTLVKASSA
>NZ_CP036280.1|WP_145445581.1|1580496_1581675_-|PEP-CTERM-sorting-domain-containing-protein
MLRNALLACCLAATPALAVPMATTSHDTSAFAFDAQLATDDLIAGKIGTELSDIEGLDGTTWSDNGWHPVNLASTFGSEWSSGLPAFTDGTNGVGSDPFYGLLNDYPGGEEATTGVPTKLVQFDLDEPSIINQINILTGNNNNADGRVFSTTMIFYSTDDGASFEQLGYFESDPLGTLNNATGDNGWKSTFVEITDSEQGPLASGVTNLRFDFYAVDNTQGQYRDPFEGENPYTGIDDELNRAVVAPLVWEIDVIGEPGVGIPNDLNGDGVVDAADIDTIAAGFGTTDPKLDIDGSGLVDVDDLNEFVTVNLGTFLGDANLDESVNLLDLSSLASNFDAAGGWADGDFNGDAGVNLLDLSILAANFENSNSVPEPAAVALLALGLAGMTRRA
>NZ_CP036280.1|WP_145445580.1|1579149_1580418_+|amidohydrolase-family-protein
MATDLDLHVDGLCVVDTHEHLNPPGLYPDQEHDPLRLLFDNYFAHDLVSAGATPGQVHDELFNPGFGGVAERFAVVAPFWERAQHTGYGRAVKIMARDLFGIERVGVETMGALEAAARALTSDPDWRLRLLRDRANLDHVQCDRFDNADEPAEPDKGFFRSDISWVWNSRGEVDFGRLMARTGVEVTGAASAREAIAEQFRREAPGAVALKSQHAYARTLLWANRTDAEVEALIERRLRGEDLVGDDRLVLGDWMFARGIEGATDHGLPVKIHTGYLAGNGGLWPTQISPSNLGPLLVGFPEARFVLMHVGYPEPGQVVQLAKHYRNTWIDMCWAWSIDPVTSRGFVASALAAVPANKILAFGGDSLWATASYAYSVQARRELAGVLGTLVADGTFDEGEAIGIATRLLRENALDLFPTPGL
>NZ_CP036280.1|WP_145445579.1|1578598_1579150_+|D-lyxose/D-mannose-family-sugar-isomerase
MQDEKVCADAVSMMADAGIRLTDRERGEIELAGFGLDNFEREGLALVVYVNGDRYCAKELVLFAGQTCPEHRHPPVELEDGRTDPGKQETFRCRAGSVYLYVEGAGDAGGIKAKVPSGSEAYYTVFHEVVLTPGDQYTIPPNTLHWFQAGPEGAVVSEFSSTSRDELDVFTDPRIQRVEAQEG
>NZ_CP036280.1|WP_145445590.1|1603793_1605782_-|sodium:solute-symporter
MEYLSTLDYAIIAVYFTVLLSFGYYLKNKAAKSLEDYFLGGRSIPWWAMGMSGMASWLDMTGTMIIVSFLYMLGPRGLYIEFRGGAVLILAFMLLWTGKWHRRSNCMTGAEWNIYRFGSGPGGQFTRVMAAITCIVATVGMLGYMVKGVGLFLAMFLPFSPSTCAIGMLGVATIYTMASGFYGVVFTDIFQSFIILFAVIAVTFIAVATQLGYEGDIATLAHEVTGSTQWTTTSLQWHTTMPSGYEAYEHLTMFALFYLIRNIMAGIASGGDPKYFGARNERECGLLSFLWGWLIMFRWPMMMGFAVLGLFMVKDAFPDQSVLATAADLIRQTLGEVPKSRWEDAVAGIINAPQLYPELVTNLQTLLGEDWATKLKLLSYEGTVNPERILPAVLMTMIPQGLKGLLLVALIAASMSTFDSTVNGATAYWTRDIYQAYLRPNAGNKELIYASYIFGVVLVAGGFAMGYSTTSINHIWDWIIMGLGSGLAIPGILRLYWWRFNAGGVVVGTVAGLTAAIVQRIYFPEWTAVQQFTILTTISLLSTIIGTLLTKPTDTAVLANFYKTTRPFGLWGPFKTLLPEDERRAMEKEHRNDIIAVPFVMTWQISLFMLPMQLVIGAYRDFLITLPIFLIGLTGMYWFWYRHLPPREPATPNEATNQTTLP
>NZ_CP036280.1|WP_145445591.1|1605847_1607467_-|hypothetical-protein
MAGRTADQHHPRHHPMRDQRTLAVSRSPSRLPQASRHEHTRSQAMTNRSGKGISTMPAITKRYTLSGIAAACILVTLLAGSARASEHKLINFTRAAGVPTGAWCWYQDERVVIDTDHPNGPMMLMGSVSFSRTDAFEHGDIDLLWHNLRTGEAGAFELHDRLQPDDHDVPALHIRDDGRYVAIYSTHSSDRIMRWRVSTHPHDPTAWEPEQTYENKVIICYSNIFKLADRDGVHQLYNFSRSDDSDPNYFVSSDRGDTFRYGGKLLTGPDGNTARGQRPYMKYASHTPEKLHFLLTDGHPRDEDNSIYHGYMSRERLHRTDGLVLGSVSRRRVSSHLAPDFTTVLATGAKFNGVEMRHAWTIDLHLDPHGHPVAAMSARANNSDLDHRFLYGRWDGSKWNVFEIAKAGGYLYKFENDYTGLMAIHPDNPDIIFISSPIDPRDDAQLQHYEIFMGRTPDKGATWAWAPVTWNSNADNLRPIVPIWKPGKTIVTWLKGGLNTYADWDSQIVGYIMDTEDLDDMVVPGQISVTRKAMSPDKP
>NZ_CP036280.1|WP_145445592.1|1607400_1609347_-|hypothetical-protein
MLALIAWLTLTGQLIMAADVMPMRWQPAAAEGPLTEYRQKVYEVVENQARYLISTTRPWEGDPTLRLLTDSKHGEHWIRPNTGTVAGLAFLYRFGPYNAERVGVSREQLLSNHIIPMMRYLVVTHKTGTRPTSNGKPWGDHWQSAHWAHMLGRSAWWIWEDLPEDLQRGIQSIMAHEADRIAAAKIPHRVKNDTKSEENGWNSQVISIAMLLLPDDPRNEVWREAFPQWAISAHLRASDATCEVIVDDRPVKDWFLGANIHEDFTLENHNIIHPDYMTCYSLGLGCALDYRMTGRAIPEALLYNVPQIYENIKWFILPDGGFVYPSGQDWRLFRNPDWHFKHVLMAVYANDPDAWSIAMRGIDTMVKMQSRPNGGAVYAPGEYFFPSAQMDLIYYTSLTWLLLHEVDELPLRPDLYTGVRRLDGGKLMLNRTPSAVHTLSWGNKIMIQAVPNQLDRIVSPHFRSGIGHVRIEGNDRAPSPKLRDIEIENTDNAFKAKLVVDHGDAIRSQITVESQPDGTFTFSEELTALKDVTTTEVGTGLIGILNNPTWVYERGYRSLTIDNDATHVPSCSGMAMERSGIHQVNIDDVLFIDSADRMNVRYASEPKPVRGRVTDHLYLNWIPGRKQWQAGQPISTTRVTIQCATNGR
>NZ_CP036280.1|WP_145445593.1|1609377_1612263_-|DUF4861-family-protein
MQIITRTTTLILTAVLGLQASTRADPMVRQYRILMPAVGTVPVFEDLDNDGDPDVLRTVLRDGMPVQWIDDDDDMTFDDLVGDTDSDCLMIDRNKDGNYGDEHDLMIDWGDEDGDNNADLQVVVENATRKDMLWGPGHYMVMVDTDQDGVLNYIDWNDYKLKCWEHTGTSHFFEDYLGHSMFLKIHTSTYNMPDLRYNWENPFLFYDEDGDDICEVAIRLVDSPRQMPAPHEGFVMPEEGSAIKDEWRRMVVDATIDWVSIATDLDNDTVPGNEFDFDMTLNYAGKGFDYADQVHRFKSLSGIREADKFFYDPRWRQLTELIYPDHDAARDLIYNRGEWGRCWLVFDEDDDCERWERVEVYHPDDPFKIGLYKGGIDWHPQSDSSGDRGEWDSDFSGGGKLYTAGFDGRIHLHGAEWGAWRIDQDAHFYQGWSRSSHTAKKFPTIRYADTDDNGFFDRIDYDLDGDKRYERSVSLISLGIDDTATLIDPAELDYQGYRDLHERVTDAMWARAQKAIEAARANQLDLSPYAGMMKPLSTRQKYHYAYWLNFYIYNDLLELAEHRGDTVFANDLDRAYFSGDWSNLTRPLVAPDPNQHAQMRIEVTNPLDQPRGHQTVEIPWQSIEDAMPHADSQTIRVINGSTGREATSQVIDTDANGTPDLLVFQHHFLASQTVVFTLQATPPVRGQNDPSPVHAKFVPTRMDDFAWESDRIAYRMYGPALRNETISNGIDVWSKRVPYPIVEKWYQPGHDYHTDRGEGADLYKVGNTLGCGGTALVIDGQFVRGENYALWRILANGPVRTLFELTFPERRINGITIRETQRLSLDKGHNLTRITTDYTIDGSPDTIEFATGLVRRNPATHSPSPDRTWLGQWGPLGAKGNGDLGAGVVLQNAGKARYEMIENHHLLLTHLPESGSVVHWAGAGWSRAHRFTDSEKWNAYLTEWAKRVNQPLMIRQIKKGK
>NZ_CP036280.1|WP_145445594.1|1612303_1613074_-|SDR-family-oxidoreductase
MSPSNSFSLEGKTALVTGCRTGIGYAIAEGLAEAGADIVGVSSTLDPLRSDVAHAVAATGRSFTGYACDMGDREALQQFIRQVRANHPVIDILVNNAGTIRRTPAAEHPDGMWDEVIGVNLTAPFILSREIGRDMLQRGHGKILFIASLLTYQGGITVPGYAASKAGIGRLTMALANEWAGRGVNVNAIAPGYIATDNTQALRDDPVRSEQILARIPAGRWGQPDDFKGPAVFLASSASDYCHGTTLLVDGGWMGR
>NZ_CP036280.1|WP_145445595.1|1613103_1614402_-|TRAP-transporter-large-permease-subunit
MNAMIQVLLLGFMALLLMGVPISVALILAAAVAITGFSDFSPGLIPLKMVGATGSFPLLAIPFFVLAGCLMDRGGMSGRLIDLARSVVGRVRGGVAMVSVIACMFFAAVSGSTAATTAAIGIVLIPAMINSGYSRGTATALQATAGSIGIIIPPSIPFVLMGVIGGISIGDLFLGGILPGILTGCVLMVIAFAIATLQRHEPSTPGTSLMAIARALLRSALPLLTVFWVLGGIVGGYVTPTEAAIVAVAWAMLVGGLIYRTLSFSDIYHALIDSTRITGIVVLCIAATAPFAWLMTVEQVPQDIAASMLSLTQNPVALKLMMLLMLLAIGTFLDLTPAMILLVPILMPIACDTIDMAPVHFGVMMVLALGIGQCTPPVGIAIFVACSVGKAEFGEVARSLVPFLAGMLLVLLVVTYWPAVTMTLPALFNGGP
>NZ_CP036280.1|WP_145445596.1|1614398_1614875_-|TRAP-transporter-small-permease-subunit
MIRKLADHLEEVAGAALLAVMCVITLIQVIGRYILTDPPAWTEELATILFTWLVFVGASLALKRNEHFVVAVFVDWLPDRLGSAARGIAHTLVAICCLVLIWYGVGLTISGHDVDTAVLELPRSWVYLAIPVGALLMLLRTISLIWRRPQAVTRETES
>NZ_CP036280.1|WP_145445597.1|1614864_1615896_-|DctP-family-TRAP-transporter-solute-binding-subunit
MTRCHPFGLIILAVTLFSMTLAGLAGCGQEPNRKPVVKIGEVLPPDHPTSDAMAYFRQRLETHTGQGVEVRRYPSGQLGNAGELIQACRTGDIEIAVVSAAPLAQYVTDMNVVALPFIFRDSQHQARVLDGEVGQTLRRSSEQAGVVALAFMDAGTRNIMTKRGPIVRPEDLKGLKIRVMDSNVLRQTIARLGATALPMSQSEVYSALQSGVIDGWENNPPTCLKFSMHETGCVYFAWTQHVAIPDVMIVSKTWYEGLSPQRREALDRAAQETSSHQRTLWAEYEVQAVEQLKQLGMRFNEVDAQAFRDRLDGAYDEYIEKYGEGFASLIEQIQNTGSPQVDP
>NZ_CP036280.1|WP_145445598.1|1615952_1616798_-|5-dehydro-4-deoxy-D-glucuronate-isomerase
MMDARLHAHETPDAQRYRGLNTRSLRSAFILDGLFQNGETRLYLTDLDRAIVGSAIPTIHPLGLPNTRTLSVDYLCQRRELGVLNIGRPGKVSVDGQEYALDGRDALYIGRGARDIRFSSDDIVDPAIFYLHSYPAHADYPTALITQSQANVVDLGSNDLANKRTINQYIHENGAPSCQLVMGYTELAVGSVWNTMPPHTHDRRTEVYTYFDVPDDQRVLHLMGRPDETRSLWIRNHQTVLSPSWSIHSGVGTAAYRFIWAMGGENQDFNDMDMLAIGDLA
>NZ_CP036280.1|WP_145445599.1|1616856_1617630_-|helix-turn-helix-domain-containing-protein
MNKYSIPNLSKACSALKWLAGETRPVSTSEVARQLSMPRTTAFRMLRTLVDEGMLEEIDGRYRSGVGLLHLGLQALNSVEVNTQADPILKRLSHDTGETAHMAVRADAQMLITKVIDSPSPIRVASRPGTLVSIHCSATGKAVLAAMKPQDRQDVLERIQFEVRTDATHSGVDSLEDDLITIRKRGYAIDDEEYFEGVRCLAATVFDAYEQPVGAIGITATTERFPKKKIPVIAAQVTAAASELSSALGQNPVLSSA

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Crispr_ID: NZ_CP036280_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_4

1968327-1968448

Orphan

Consensus_repeat	Method
CTGCTGGATCTGTCGATCCTCGCGAGCAACTTCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036280_4

>merge|NZ_CP036280|4|1968327-1968448|CRISPRCasFinder
CTGCTGGATCTGTCGATCCTCGCGAGCAACTTCGGCGGGCCTGGCATCTATCTGGACGGCGACTTCAATGGCGACGGGGTCGTGGACCTGCTGGACCTGTCGATCCTCGCGAGCAACTTCGG

>NZ_CP036280|4|4|1968327-1968448|CRISPRCasFinder
CTGCTGGATCTGTCGATCCTCGCGAGCAACTTCGG	CGGGCCTGGCATCTATCTGGACGGCGACTTCAATGGCGACGGGGTCGTGGAC
CTGCTGGACCTGTCGATCCTCGCGAGCAACTTCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145445920.1\|1971722_1972496_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|225076
NZ_CP036280.1\|WP_145445899.1\|1956691_1958035_-\|N-succinylarginine-dihydrolase	unknown	unknown	gnl\|CDD\|237332
NZ_CP036280.1\|WP_145445909.1\|1965397_1966228_-\|MlaE-family-lipid-ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|376777
NZ_CP036280.1\|WP_145447246.1\|1976312_1977095_+\|GTP-cyclohydrolase-I-FolE2	unknown	unknown	gnl\|CDD\|237466
NZ_CP036280.1\|WP_145447245.1\|1973099_1975454_-\|endopeptidase-La	unknown	unknown	gnl\|CDD\|223542
NZ_CP036280.1\|WP_145445922.1\|1972498_1973074_-\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	unknown	unknown	gnl\|CDD\|376665
NZ_CP036280.1\|WP_145445903.1\|1959510_1960527_-\|arginine-N-succinyltransferase	unknown	unknown	gnl\|CDD\|377426
NZ_CP036280.1\|WP_145445918.1\|1970465_1971722_+\|RluA-family-pseudouridine-synthase	unknown	unknown	gnl\|CDD\|223638
NZ_CP036280.1\|WP_145445898.1\|1954969_1955830_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|380381
NZ_CP036280.1\|WP_145445913.1\|1968640_1969132_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145445915.1\|1969218_1969701_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145445905.1\|1960523_1961396_-\|ion-transporter	unknown	unknown	gnl\|CDD\|366146
NZ_CP036280.1\|WP_145445907.1\|1961434_1965166_-\|LEPR-XLL-domain-containing-protein	unknown	unknown	gnl\|CDD\|214807
NZ_CP036280.1\|WP_145445896.1\|1953133_1954783_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271213
NZ_CP036280.1\|WP_145445894.1\|1951664_1953038_-\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|376421
NZ_CP036280.1\|WP_145445916.1\|1969739_1970453_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145447244.1\|1955875_1956685_+\|phytanoyl-CoA-dioxygenase-family-protein	unknown	unknown	gnl\|CDD\|368580
NZ_CP036280.1\|WP_145445901.1\|1958031_1959504_-\|succinylglutamate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|181873
NZ_CP036280.1\|WP_145445926.1\|1977102_1978035_-\|protease-modulator-HflC	unknown	unknown	gnl\|CDD\|259803
NZ_CP036280.1\|WP_145445924.1\|1975704_1976121_-\|Hsp20-family-protein	unknown	unknown	gnl\|CDD\|223149

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145445922.1\|1972498_1973074_-\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	gnl\|CDD\|376665	pfam01923, Cob_adeno_trans, Cobalamin adenosyltransferase. Cobalamin adenosyltransferase This family contains the gene products of PduO and EutT which are both cobalamin adenosyltransferases. PduO is a protein with ATP:cob(I)alamin adenosyltransferase activity. The main role of this protein is the conversion of inactive cobalamins to AdoCbl for 1,2-propanediol degradation.The EutT enzyme appears to be an adenosyl transferase, converting CNB12 to AdoB12.	4.61163e-76
NZ_CP036280.1\|WP_145445899.1\|1956691_1958035_-\|N-succinylarginine-dihydrolase	gnl\|CDD\|237332	PRK13281, PRK13281, N-succinylarginine dihydrolase.	0
NZ_CP036280.1\|WP_145445909.1\|1965397_1966228_-\|MlaE-family-lipid-ABC-transporter-permease-subunit	gnl\|CDD\|376777	pfam02405, MlaE, Permease MlaE. MlaE is a permease which in E. coli is a component of the Mla pathway, an ABC transport system that functions to maintain the asymmetry of the outer membrane. In NMB1965 it is involved in L-glutamate import into the cell. In Arabidopsis thaliana TGD1 it is involved in lipid transfer within the cell.	3.39171e-80
NZ_CP036280.1\|WP_145447245.1\|1973099_1975454_-\|endopeptidase-La	gnl\|CDD\|223542	COG0466, Lon, ATP-dependent Lon protease, bacterial type [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP036280.1\|WP_145447246.1\|1976312_1977095_+\|GTP-cyclohydrolase-I-FolE2	gnl\|CDD\|237466	PRK13674, PRK13674, GTP cyclohydrolase I FolE2.	4.50138e-132
NZ_CP036280.1\|WP_145445903.1\|1959510_1960527_-\|arginine-N-succinyltransferase	gnl\|CDD\|377426	pfam04958, AstA, Arginine N-succinyltransferase beta subunit. Arginine N-succinyltransferase EC:2.3.1.109 catalyzes the transfer of succinyl-CoA to arginine to produce succinyl-arginine. This is the first step in arginine catabolism by the arginine succinyltransferase pathway.	1.3444e-150
NZ_CP036280.1\|WP_145445907.1\|1961434_1965166_-\|LEPR-XLL-domain-containing-protein	gnl\|CDD\|214807	smart00758, PA14, domain in bacterial beta-glucosidases other glycosidases, glycosyltransferases, proteases, amidases, yeast adhesins, and bacterial toxins.	6.17491e-13
NZ_CP036280.1\|WP_145445898.1\|1954969_1955830_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|380381	cd06976, cupin_MtlR-like_N, AraC/XylS family transcriptional regulators similar to MtlR, N-terminal cupin domain. MtlR is a Pseudomonas fluorescens protein that acts as a transcriptional regulator of the mannitol utilization genes. It has an N-terminal cupin domain (represented by this alignment) and a C-terminal AraC/XylS family helix-turn-helix (HTH) DNA-binding domain. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	1.5913e-36
NZ_CP036280.1\|WP_145445905.1\|1960523_1961396_-\|ion-transporter	gnl\|CDD\|366146	pfam00520, Ion_trans, Ion transport protein. This family contains sodium, potassium and calcium ion channels. This family is 6 transmembrane helices in which the last two helices flank a loop which determines ion selectivity. In some sub-families (e.g. Na channels) the domain is repeated four times, whereas in others (e.g. K channels) the protein forms as a tetramer in the membrane.	2.41444e-37
NZ_CP036280.1\|WP_145445918.1\|1970465_1971722_+\|RluA-family-pseudouridine-synthase	gnl\|CDD\|223638	COG0564, RluA, Pseudouridylate synthases, 23S RNA-specific [Translation, ribosomal structure and biogenesis].	9.31357e-94
NZ_CP036280.1\|WP_145445896.1\|1953133_1954783_-\|hypothetical-protein	gnl\|CDD\|271213	cd14254, Dockerin_II, Type II dockerin repeat domain. Bacterial cohesin domains bind to a complementary protein domain named dockerin, and this interaction is required for the formation of the cellulosome, a cellulose-degrading complex. The cellulosome consists of scaffoldin, a noncatalytic scaffolding polypeptide, that comprises repeating cohesion modules and a single carbohydrate-binding module (CBM). Specific calcium-dependent interactions between cohesins and dockerins appear to be essential for cellulosome assembly. This subfamily represents type II dockerins, which are responsible for mediating attachment of the cellulosome complex to the bacterial cell wall.	8.20937e-11
NZ_CP036280.1\|WP_145445894.1\|1951664_1953038_-\|PEP-CTERM-sorting-domain-containing-protein	gnl\|CDD\|376421	pfam00932, LTD, Lamin Tail Domain. The lamin-tail domain (LTD), which has an immunoglobulin (Ig) fold, is found in Nuclear Lamins, Chlo1887 from Chloroflexus, and several bacterial proteins where it occurs with membrane associated hydrolases of the metallo-beta-lactamase,synaptojanin, and calcineurin-like phosphoesterase superfamilies.	6.69393e-18
NZ_CP036280.1\|WP_145445920.1\|1971722_1972496_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|225076	COG2165, PulG, Type II secretory pathway, pseudopilin PulG [Cell motility and secretion / Intracellular trafficking and secretion].	1.49076e-09
NZ_CP036280.1\|WP_145447244.1\|1955875_1956685_+\|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.	4.04861e-22
NZ_CP036280.1\|WP_145445901.1\|1958031_1959504_-\|succinylglutamate-semialdehyde-dehydrogenase	gnl\|CDD\|181873	PRK09457, astD, succinylglutamic semialdehyde dehydrogenase; Reviewed.	0
NZ_CP036280.1\|WP_145445926.1\|1977102_1978035_-\|protease-modulator-HflC	gnl\|CDD\|259803	cd03405, SPFH_HflC, High frequency of lysogenization C (HflC) family; SPFH (stomatin, prohibitin, flotillin, and HflK/C) superfamily. This model characterizes proteins similar to prokaryotic HflC (High frequency of lysogenization C). Although many members of the SPFH (or band 7) superfamily are lipid raft associated, prokaryote plasma membranes lack cholesterol and are unlikely to have lipid raft domains. Individual proteins of this SPFH domain superfamily may cluster to form membrane microdomains which may in turn recruit multiprotein complexes. Escherichia coli HflC is an integral membrane protein which may localize to the plasma membrane. HflC associates with another SPFH superfamily member (HflK) to form an HflKC complex. HflKC interacts with FtsH in a large complex termed the FtsH holo-enzyme. FtsH is an AAA ATP-dependent protease which exerts progressive proteolysis against membrane-embedded and soluble substrate proteins. HflKC can modulate the activity of FtsH. HflKC plays a role in the decision between lysogenic and lytic cycle growth during lambda phage infection.	6.09293e-117
NZ_CP036280.1\|WP_145445924.1\|1975704_1976121_-\|Hsp20-family-protein	gnl\|CDD\|223149	COG0071, IbpA, Molecular chaperone (small heat shock protein) [Posttranslational modification, protein turnover, chaperones].	9.53208e-17

>NZ_CP036280.1|WP_145445909.1|1965397_1966228_-|MlaE-family-lipid-ABC-transporter-permease-subunit
MIKTVASLGAAAEFNLDRFGLFTRFCLTTANWAVRWMVGRSRLYLLMPQFYAIGTRSIPVVMLVGLFVGAVLGVEAFDQFEAIGQESRLGGIIGISVLRQIGPVLAAVMIAGRVGGAISAELGSMKVTEQIDAIRVMGADPIDYLVVPRVIACLIMVPILTVFSNLMGVYGGHLVCVNALGVDSREYWDFSARFIGNWDVFTGLGKALIFGLAIGLIACYKGFHCGSGAQGVGRAATDAFVTSFIAIIVLNFFLAKFFKDIYVILFGHGGPTAFMG
>NZ_CP036280.1|WP_145445907.1|1961434_1965166_-|LEPR-XLL-domain-containing-protein
MANRHHHQTVRGLEPLEPRLMLAADAPIPDFHVPEPVYEVAFEAGVQHNASTQVHAAHDGMGHTLMALLPDAATNTVAVRSGLWSDPDTWGGALPQSDDVVVIPGGIDIVYDMVSDTSYRGVRVDHGARFEFHTEINTRLVVDTFVAMPGSAFSMGSEDRPIQPDVRAELLIDPSRGAITDPQLIGRGLLTHGNTTIVGSDKIDFLPLALHPSAGDQTLVLDGRPDGWRVGDILVLTGTTTDPDGSNDDNSRFHDEVLRVTSITERANQTLVTFHNLTQEADGKLDSLLWDHHPPEGFDDWDLTVYAANMTRNVLIQTLDADQTLTQQRGHTMFMHSAQVVIRNASFYDLGRSDKNRLVDEPVVNVDGTPGNGTNQRGRYALHLHRLGAGDLATTPAVVAGNAVWGSPGWGIVHHDSHANLSDNVVFDVVGSAIVAEDGNEIGTWSNNLTIKTTGDDRPELDFDLSPRVPLFDFGFNGEGFWLQGAGQILMDGNIAASSASAGIMLFSNVDAMRSVKIPAAVLEHPEITQGDAAVDAFNVPARGIFDSTVLNAEFGLITWGHMRNQDGELGFTFGLETPAHRLRTTIEDFAFWAIRGDGIFTQYTSQTDFRNGLILGDLDDPVAYRTGINGEGRGRGVGSNTASKNLTYDNLHIEGFEIGLRLLAEGMASADEQHDPSPARNAASRLLNSTIRNVDVPLQIFGAFHNTTSIDPHYFVIDNTAFEARSPHSVPAYAHFESTLLATNAFELDASDSYHVDTRAIDSIGIASYGWDFDADGVNDAFGRKVRHTFDSAGPKPVTLTIVDTAGRSTSVTRTLDARPAALVNPLGDGTFDDAEDIFTGYDWRRPTSADEGLGWVNYGWTVDDGVATRLPGSNEINHALNQVVRDQNITRGVKTLSFEAGMIEQAGEDAQLRAVVYGVNAPEFVLPHYSDGPPVPIFGLEGEVDRLLDSGDLLNGTTPTTAFELEIDFGQGYEFIVVVFESLHVSTAQGDQLWLDNIRIEDSAPVPSAPFITSRELPAIAMGTPIDIQLEAHGGNGDRVWAAATNLLPEGLTLTSDGRLTGTATEAGSFTLYANVRDDDRQFSSVQIPFRIIEPPVGSEAGLAYEVYVNHTQHTVQGLTESELLLSGTTTELSTGLFPPGVAGQVGIRWHGYLWIDTPGLYAFTSTSDDGSQLRIGDNLVVDNDGVHGVKTVTGTINLDAGFYPFELLYFDWGGGQQLHVTMSGPGGVQGAIAGLRMSHT
>NZ_CP036280.1|WP_145445905.1|1960523_1961396_-|ion-transporter
MLILKIRELVNSKLFGQAILGLILVAAVIVGLETYPEVMARYGDLIHTIDWVIITLFALEAILKMAQHGRHWYRYFYDPWNVFDFSIVVVCLLPVGGHAAAITRLVRVLRALRLISTLPKLQLLVEALLRSVPSMVYVGVLLVILFYIYAVMGVFAFRENDPVHFGNLQLALLSLFRIVTLEDWTDIMYIQMYGSDVFAIDNPAAQPEQPSAQPMLAVVYFVSFVLFGTMIMLNLFIGVIITSMEEAQAEAEARKEHPTVDDEFVELARDVDNIKLRLQAIRRHVSEKQP
>NZ_CP036280.1|WP_145445903.1|1959510_1960527_-|arginine-N-succinyltransferase
MTPQLRPRLRLVNNGDLDALLNLAHQSGHGLTSLAADRDSLAERIEKSRSGKSRLFVLEEPENQRVVGSSGITCQVGIGEPWYSYRKETLTHHSQGLGITHNVEVLHRKLFYNGPTEVGTLFLSPSARGGGTGRFLSLARFLYVAQFPDQFQPEVFAEMRGVSDAAGRSPFWDAVGRHFYTLDYSDADFRSAHDKQFIAELMPRHPIYLTLLPDAATSVVGKAHPDTQPALHLLMQEGFQHGDLVDIFDAGPIVTCPTQQIRTVRDSRIWRWTTDVPADANELWMIGNTRDTFLATFAPARPEGDTLQIPHDVAATLDLESGEPIRAVRLRPDYNNES
>NZ_CP036280.1|WP_145445901.1|1958031_1959504_-|succinylglutamate-semialdehyde-dehydrogenase
MTPGQHLINGNWAAGTGAPLQAHNPWSLEPTWQGNAASGDQVDEAVQAARDAHPAWAATPLDQRIEIAQRYAELAKQHTEEIALAIAREAGKPLWEARGEAALLAPKVATSIEEHRRQLADRTIDLPNGRGVTRYRPHGLLAVIGPFNFPIHLPNGHITPALLAGNTIVFKPSERTPTAGMIMAELWQKAGLPQGVLSAVVGARDTGQALVQHPQTDGVLFTGSYPAGRSIAASLVDEPGKIVALELGGNNPIVVHDTNHLDTAAYITAVSAFSTAGQRCNCARRVILTDSIDRDAFLDRLTGIARSITVGPFDAEPAPFCGPLITPQAGQAILDAQQQLLDFGAAPVLPLEVAGPHTGILTPGILAIEPDKRPDEEYFGPLLSVLTTRTLDDAIALANQTRYGLAASLLTDNAEHFDRFVHTVRAGIINLNGPTVGASGKMPFGGIGRSGNHRPSASAAAAYCAFPVASMEAGPLAPVDKPLPGITPSS
>NZ_CP036280.1|WP_145445899.1|1956691_1958035_-|N-succinylarginine-dihydrolase
MTTTEFQFDGLVGPTHNYAGLAPGNLASQTHRGDTASPRAAVLQGIDKAATLARLGIPQAVLPPHERPHLDLLRAAGFTGTDADLLHAAQRHAPELLAAAWSASAMWTANAATVSPAPDTADQRLHLSPANLTSALHRSLEAPFTTRLLRRIFADDTRFAVHDPLPAALTDEGAANHTRLAPTHDNPGIEIFTYGTAAPRGTSPGPEPRRFNARQRLAASQAVARRHQLDPQRTLFLQQHPDAIDAGVFHNDVIAVGDTDLLLLHEHAYIDTDDAISQITETWNRHHAQPLIILRVHPDEVSLEDAVSSYLFNSQLLRTPDGQRLIVCPENCRQSPAVSRLLEDWQTQGLIHEALFFDLQQSMSNGGGPACLRLRVVLTDHQQAAIPQSLLLTERRAAQLRDWAHRTYPETLTPDDLADPKLITIARDALDELTRILNLSNLYDFQR
>NZ_CP036280.1|WP_145447244.1|1955875_1956685_+|phytanoyl-CoA-dioxygenase-family-protein
MTEALDQPFALSATHLERFAKFGYVKIPGVLSPELLEAVREPIGRVVQANNKHAGVPIEERDTYGKAFIQVTNIWEQSEEARRFVMGKRLGRIAAELLGVAGVRLYHDQALYKEPSGGITPWHLDQYYWPLATDRTVTVWIPLVEIPIEMGPLSFAAGSQELDFGRDMAISDDSETALRDALEREAYPVEASAYALGEVSFHLGWTAHRAGPNRGERAREVMTMIYMDRDMTLMEPKHENQRHDREVFCPGIEVGAVCDSPKNPIVYEA
>NZ_CP036280.1|WP_145445898.1|1954969_1955830_+|helix-turn-helix-domain-containing-protein
MEPLLEHLTPTPQSSFRLYTRVDDHFSFEWHHHPEYELTLILEGYGRRFVGDSIHGYEAGDLVLIGPYLPHTWQSDESSSDNTAVVIHFTEAWVKQGVGSWPELQYLARMLDRSTHGLLFDERTRARAAEGLKALSSMSGLGRLARLLEVLYGLASDPKARTIASPGYRRSSRPIDPRIDRVCRFVNDRINEELTQREVAAMIRMKPTSFSRLFKRAMGKTFIEYVHELRIANACRGLVESDDPITDVCFRSGFNNVSNFNRVFRRLVGVSPRAYRRQFHEPAARA
>NZ_CP036280.1|WP_145445896.1|1953133_1954783_-|hypothetical-protein
MLKTRSLLALALALSTSAASGQVVINEFIYDTNNYDAEDTNREFVELYNAGNGPVDISGWTLDAWDTVDSDGLSGLNASFEIPAGTTLAAGDFYVMGWGSVPNVDQVLTPYYNTPNGNGSQAKQGLFEDRSETIELYSNTGVLQDAVRYEVNKWVSGADANQIFIPAEVFAEIGAGPDIDETNPSASTVPGGLWSNFQSIRADGNISVSRYIDGHDTNVNGYDFGAFKATPGAPNALPSVPQHVVPDVDGLAEGATLTEYTESWVAATVIDPTVVSTLNPTVIVPSPQGGNAIAVSDSSGGTMVAGQELVDKIDIYAYLETSVVTRADGNTPQESTMFGIGTTDANFNIPDPEDKLGATGSNVNGSTGLAWLFLRTDVDATLYLVDAKQGGRDYDTWDILAQYDLTDEAADWARLSIDAENGVATYNDEIINFDAQPDLLGTFYVGFNEFVDGRATRPATWDMVSSVVSLPGDANGDGLVNLLDLSVLASNFDGTDTPYTNADGDFNGDGLVNLLDLSILATNFETTQTPEPAGAALIGLGALALIRRR
>NZ_CP036280.1|WP_145445894.1|1951664_1953038_-|PEP-CTERM-sorting-domain-containing-protein
MERVTTSTLLIAALMGFGANADAQVYVNEVLYDLDVNDNSGSSEPDGEFIELYNAGTADVDLSGWVLDTRDPFGAGPNYPLPAGSIIPAGGYFVVGSANVPNVDYTPLPRPASGLASQDQGYMEDRNETVELYDAAGALIDAVAFETSKGIATTDPVIGAQLGGGIYASQSLVPGVGVGQSMSRYLDGVDTDVNGYDFGQLPQTPGASNNLPQVVSHNVPDVDGLATGTTLTGDYTASYINPEVIDPTVVSAMNPTAIPASPQGGNAIAMADFGGTFATSNELVDGFDIYAYIDTNPTPLRGGANPSAESTMFGIGNSGIFFNVPDPASRLSVGSGINGSTGLAWLISRSEVDVFLYLVDAKNGGQNSTWDILAEFDLTGVDADWARLSIDAENGVAMYNDNVVNFDAQPELLGPFYAGHNEFIDGFASRPATWDVVPEPASLALTGLGCLAMLRRR
>NZ_CP036280.1|WP_145445913.1|1968640_1969132_+|hypothetical-protein
MIKYLVMLSLVLCVAGCEAMESMGVIGPKSEHPVEKFVFDTGGDKHAEGFGGWRIEYTRGGKMSLTHTIGEDATTYGPLSLSSDVASTVWEAVDRLPFDRLSSDQTEAVPGDLPYYFGWTMNGKARSASLPSSAALKEPMVLAMNALLGEVIEAQTGVEPVLE
>NZ_CP036280.1|WP_145445915.1|1969218_1969701_+|hypothetical-protein
MMHRWFASLIAVATVCVGLLGCEGPALVYTDDGVLLQPQRGSGLVPKLESNWLIPDVPTPIGFQPLTSQCMATTDGMTRTVTHVYQGRTNISDAVKFYRQNLRDPRLGWVFEGVGRTDDGVQILDYTKGAEAMQIRILTDAGLTTIQVDITPLDMAPAAS
>NZ_CP036280.1|WP_145445916.1|1969739_1970453_+|hypothetical-protein
MAKRPVEPEAPESLHEVWLINLQVLYTKHQNKIAVALLLAALFFIGRWAYTDYQIRQLEDSWGRMATATSPVSFRNIAEDYAGQTVANHASLSAADLLLSEATRVRTAESDEVDVESNLQQAEGLYQEVLSSSEHDLIKANALFGLAAIAECRLAWDDAQGHYETIERLAAERYPFLASMAAERSAVIPELQKGVVIEETSILDELGVGGEEAPESEAAEAAKPVSEEAETAEPVAE
>NZ_CP036280.1|WP_145445918.1|1970465_1971722_+|RluA-family-pseudouridine-synthase
MSDPEHDGLTDGGEDELDIDAWEASGGDVQSYRLSKNARFRLDKYVQNRVKGLSRNQIQKLITLEAITVNQKKAKASLMLKEGDVVDIRLPPKPGSTIEPEEIPLDILYEDEDIIVINKQAGIVVHPARSYLSGTMLNALAHHFVATGQSSGAEQPEVPADADDELTLVPGLSAVGADDARPGVVHRLDKNTTGVIVFAKRDFSHWMVAKQFEDRTNLKAYLAVVHGCPEPEGGAIDQPIGKHPTIKEAYAIRQEPYGKPSLTLYRVRERYKGYSLVELELKTGRTHQIRVHLSYLGHPIVGDVLYGGEPVGNTEITEPVMPAGYRPYVNFARDKEEGRRIESAAAEREDLIIGHPALHATLLRIRQPISDEEMTFTAPVHHAMRVLLAKLRNHLDDGPVVMQGYHVDLTKATPAPDG
>NZ_CP036280.1|WP_145445920.1|1971722_1972496_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MESAVVLTEGAEVRPRAWHSGFTLIELLVVISIIAILIGILMPSLSSARNAAKTVSCLNNEKQHIIATSVHTTDHDGFFPWTNWDNGRQNASANIPAGWLYDVDRRVNPGGEYVPEDLETGTMFRYIRTSDMWRCPLDEPEEDAPGSRKITSYVMNGAINSYTQRQDIPPVRVSHLRGNALIFWELDEEAPAGAWNDGSNSPDEGISRRHQGSGTATFVDGSVRTIPWDQWIEDLTVAPGPLWCDPRLEDGGYSRFF
>NZ_CP036280.1|WP_145445922.1|1972498_1973074_-|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase
MKLYTRTGDDGTTALFGGQRVAKDALRVEVYGAVDELNAGLGLAITAAANPAHKGLVETLARVQSDLFDLGAHLATPDDTREEVRARLPVFEQATITGLERAIDEATQPVEELRAFILPGGCETAARLHHARTVCRRAERLAVQLADAEPIHPLAVTYLNRLSDLLFALARLANHNESHPETTWQPRRTEG
>NZ_CP036280.1|WP_145447245.1|1973099_1975454_-|endopeptidase-La
MPSELPILPLRGTVVFPGTITPISIGRASSRQLLDESLATSKFIGLFTQREETEEEPGIDDLYEMGTAAMVLKLVRQPDENLSIIVHGLKRVRALKATKTNPYLRAQVEEPSERPGSSKTFDAAIAQLREQARQLIELSPNAPEQALTVLLNIDDPGNLADFLAANIDLSVEQKQDILELTDVAKRVRAIHHHVSSRLQLAQLQAKIQEDVEIAIGDNQRKFFLREQIKAMQKELGEDTGDGEQLITRLREQLEQAAPPEAVMEEAQRELTRLEAIPPASPEHSVISSYIELIAELPWNTASEENLDLIEARAILDRDHFDLDKVKRRLIEYLAVRKLNPDSRGPILCLVGPPGVGKTSLGQSIADAMGRKFARLSLGGVRDEAEIRGHRRTYVGAMPGRIIQAIRRAGTNNPVLMLDEIDKLGADFRGDPASALLELLDPRQNNAFVDRYLDVPFDLSAVLFIATANYMGHVPPALHDRLEVIEIPGYTDHDKAAIARKYLIPRQLKEHGLRRSQCRWAAPAIHTVIEHYTREAGVRELDRQIAAVCRNVASEVASRPRRKGSRARTANGKPDSRSVTPDLVREALGPEKYVREIDDRTKPPGVATGLAYTPVGGEVLYVEAAAFPGKGGFKLTGQIGDVMKESAAAALSLFRGRAEALGYDPDKLAETDIHIHVPAGAIPKDGPSAGTSMFTAIASLLLDKPVRGRLAMTGEITLRGKVLPVGGIKEKTLAAERAGVRTVLLPKLNERDLEEIDPRVRKRLKFRFVDTIDQILDHALGVKTR
>NZ_CP036280.1|WP_145445924.1|1975704_1976121_-|Hsp20-family-protein
MDELMETGWFRGDEACSFDSSWSPAINVFRTPTELHVCLDLAGVEPTSISVEFAEGQLVVRGERVCPQPEIVDPSKGRIEVMEIDYGSFVRVIEVPVRLDLTSVRQVYDRGLMHLTLPLVSRTETEIPGSTETPSSVG
>NZ_CP036280.1|WP_145447246.1|1976312_1977095_+|GTP-cyclohydrolase-I-FolE2
MPDVQGSRDERNIAINRVGVKGVRYPITLLDRKSGGEQHTVAMVDMYVALPADQKGTHMSRFLEVLNAHHRSIHSDDVMAMCREMKQRLDAEEAHLQVTFPYFIDKPAPVSGQVGKIDVEVTFTCTTTGNTDDFILGVKVPATSLCPCSKEISAYGAHNQRCEMMVEVRVAEDAVMWVEDLVKVAENAASTQVFSVLKRPDEKYVTEAAYDNPKFVEDIVRDLALALESDDRVTWYRVDSENYESIHNHNAFACIERDKQ
>NZ_CP036280.1|WP_145445926.1|1977102_1978035_-|protease-modulator-HflC
MIRGLAIILFFIVIIVLAGSLYQLDETEQAVILRFQQPVGNAVTEAGIHFKLPFIDDVRRFDKRLLAWDGDPNQIPTLERQFIKIDTTARWRIIDPLLFLQRVRDESGAQSRLDDVIDSVVRDSVSSTNLAQLVQSSDWAGGVISDSQNPPASEGDQPAGREELEALILRKASANMDQFGIELVDVRIKRVNYVPSVQARVFDRMITERQRVAQQYRSEGEGEASRIQGETQRDLAQITSSAQRDAEIIRGKADAEATNIYAGAYGKDPEFYAFMRTLESYSKTLSGGTTLLLSADAPYFHYLKGEKLED

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Crispr_ID: NZ_CP036280_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_5

2249427-2249685

Orphan

Consensus_repeat	Method
GGCGAGGATGGAGAGGTCGAGGAGGTCG	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP036280_5

>merge|NZ_CP036280|5|2249427-2249685|CRISPRCasFinder
GTCGACGATGACGATGCCGAGTTGGTCGGGGGTGGTGTGCATGGGGACATATTAGGACCGTCGTCTACGGAGGGCAGGGAGCAGGAGGAGGAGGGTGATGAGGGCGGGTTCGGGGATGGCGTTGAGGCTGGTGCCGAAGTTGCTGGCGAGGATGGAGAGGTCGAGGAGGTCGGCTCTCTCGTCGCCGTTGAAGTCGGCGGTGCTCCAGTCAGCGTTCTGGTTGAAGTTGGAGGCGAGGATGGAGAGGTCGAGGAGGTCG

>NZ_CP036280|5|5|2249427-2249685|CRISPRCasFinder
GTCGACGATGACGATGCCGAGTTGGTCG	GGGGTGGTGTGCATGGGGACATATTAGGACCGTCGTCTACGGAGGGCAGGGAGCAGGAGGAGGAG
GGTGATGAGGGCGGGTTCGGGGATGGCG	TTGAGGCTGGTGCCGAAGTTGCT
GGCGAGGATGGAGAGGTCGAGGAGGTCG	GCTCTCTCGTCGCCGTTGAAGTCGGCGGTGCTCCAGTCAGCGTTCTGGTTGAAGTTGGA
GGCGAGGATGGAGAGGTCGAGGAGGTCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145446172.1\|2246084_2246699_-\|methyltransferase	unknown	unknown	gnl\|CDD\|223813
NZ_CP036280.1\|WP_145446174.1\|2247696_2248995_+\|histidine--tRNA-ligase	unknown	unknown	gnl\|CDD\|273080
NZ_CP036280.1\|WP_145446171.1\|2244450_2246088_+\|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase	unknown	unknown	gnl\|CDD\|293734
NZ_CP036280.1\|WP_145446183.1\|2257391_2258393_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP036280.1\|WP_145446166.1\|2240671_2241349_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446177.1\|2251487_2252609_+\|3-isopropylmalate-dehydrogenase	unknown	unknown	gnl\|CDD\|179579
NZ_CP036280.1\|WP_145446168.1\|2242718_2243051_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446173.1\|2246782_2247700_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379312
NZ_CP036280.1\|WP_145446179.1\|2253891_2255160_-\|methyltransferase	unknown	unknown	gnl\|CDD\|239425
NZ_CP036280.1\|WP_145446180.1\|2255228_2255666_-\|CBS-domain-containing-protein	unknown	unknown	gnl\|CDD\|341391
NZ_CP036280.1\|WP_145447261.1\|2260942_2261548_+\|redoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239267
NZ_CP036280.1\|WP_145446167.1\|2241517_2242675_-\|biotin-synthase-BioB	unknown	unknown	gnl\|CDD\|273075
NZ_CP036280.1\|WP_145446181.1\|2255839_2256334_-\|transcriptional-repressor-NrdR	unknown	unknown	gnl\|CDD\|234774
NZ_CP036280.1\|WP_145446170.1\|2243684_2244344_+\|glycerol-3-phosphate-1-O-acyltransferase-PlsY	unknown	unknown	gnl\|CDD\|234691
NZ_CP036280.1\|WP_145446182.1\|2256358_2257249_+\|YmdB-family-metallophosphoesterase	unknown	unknown	gnl\|CDD\|379099
NZ_CP036280.1\|WP_145446169.1\|2243081_2243396_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446178.1\|2252609_2253845_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|213815
NZ_CP036280.1\|WP_145446185.1\|2259436_2260882_+\|dihydrolipoyl-dehydrogenase	unknown	unknown	gnl\|CDD\|235798
NZ_CP036280.1\|WP_145446165.1\|2239972_2240455_-\|D-tyrosyl-tRNA(Tyr)-deacylase	unknown	unknown	gnl\|CDD\|235383
NZ_CP036280.1\|WP_145446184.1\|2258397_2259279_-\|formyltetrahydrofolate-deformylase	unknown	unknown	gnl\|CDD\|235676

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145446172.1\|2246084_2246699_-\|methyltransferase	gnl\|CDD\|223813	COG0742, COG0742, N6-adenine-specific methylase [DNA replication, recombination, and repair].	1.26447e-46
NZ_CP036280.1\|WP_145446174.1\|2247696_2248995_+\|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].	7.73878e-108
NZ_CP036280.1\|WP_145446171.1\|2244450_2246088_+\|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase	gnl\|CDD\|293734	cd16010, iPGM, 2 3 bisphosphoglycerate independent phosphoglycerate mutase iPGM. The 2,3-diphosphoglycerate- independent phosphoglycerate mutase (iPGM) catalyzes the interconversion of 3-phosphoglycerate (3PGA) and 2-phosphoglycerate (2PGA). They are the predominant PGM in plants and some other bacteria, including endospore forming Gram-positive bacteria and their close relatives. The two steps catalysis is a phosphatase reaction removing the phosphate from 2- or 3-phosphoglycerate, generating an enzyme-bound phosphoserine intermediate, followed by a phosphotransferase reaction as the phosphate is transferred from the enzyme back to the glycerate moiety. The iPGM exists as a dimer, each monomer binding 2 magnesium atoms, which are essential for enzymatic activity.	0
NZ_CP036280.1\|WP_145446183.1\|2257391_2258393_+\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	9.88725e-50
NZ_CP036280.1\|WP_145446177.1\|2251487_2252609_+\|3-isopropylmalate-dehydrogenase	gnl\|CDD\|179579	PRK03437, PRK03437, 3-isopropylmalate dehydrogenase; Provisional.	4.86152e-178
NZ_CP036280.1\|WP_145446165.1\|2239972_2240455_-\|D-tyrosyl-tRNA(Tyr)-deacylase	gnl\|CDD\|235383	PRK05273, PRK05273, D-tyrosyl-tRNA(Tyr) deacylase; Provisional.	1.10703e-90
NZ_CP036280.1\|WP_145446173.1\|2246782_2247700_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	3.66904e-05
NZ_CP036280.1\|WP_145446179.1\|2253891_2255160_-\|methyltransferase	gnl\|CDD\|239425	cd03309, CmuC_like, CmuC_like. Proteins similar to the putative corrinoid methyltransferase CmuC. Its function has been inferred from sequence similarity to the methyltransferases CmuA and MtaA. Mutants of Methylobacterium sp. disrupted in cmuC and purU appear deficient in some step of chloromethane metabolism.	5.16334e-17
NZ_CP036280.1\|WP_145446180.1\|2255228_2255666_-\|CBS-domain-containing-protein	gnl\|CDD\|341391	cd04623, CBS_pair_bac_euk, Two tandem repeats of the cystathionine beta-synthase (CBS pair) domains present in bacteria and eukaryotes. The CBS domain, named after human CBS, is a small domain originally identified in cystathionine beta-synthase and is subsequently found in a wide range of different proteins. CBS domains usually occur in tandem repeats. They associate to form a so-called Bateman domain or a CBS pair based on crystallographic studies in bacteria. The CBS pair was used as a basis for this cd hierarchy since the human CBS proteins can adopt the typical core structure and form an intramolecular CBS pair. The interface between the two CBS domains forms a cleft that is a potential ligand binding site. The CBS pair coexists with a variety of other functional domains and this has been used to help in its classification here. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown. Mutations of conserved residues within this domain are associated with a variety of human hereditary diseases, including congenital myotonia, idiopathic generalized epilepsy, hypercalciuric nephrolithiasis, and classic Bartter syndrome (CLC chloride channel family members), Wolff-Parkinson-White syndrome (gamma 2 subunit of AMP-activated protein kinase), retinitis pigmentosa (IMP dehydrogenase-1), and homocystinuria (cystathionine beta-synthase).	1.44238e-46
NZ_CP036280.1\|WP_145447261.1\|2260942_2261548_+\|redoxin-domain-containing-protein	gnl\|CDD\|239267	cd02969, PRX_like1, Peroxiredoxin (PRX)-like 1 family; hypothetical proteins that show sequence similarity to PRXs. Members of this group contain a conserved cysteine that aligns to the first cysteine in the CXXC motif of TRX. This does not correspond to the peroxidatic cysteine found in PRXs, which aligns to the second cysteine in the CXXC motif of TRX. In addition, these proteins do not contain the other two conserved residues of the catalytic triad of PRX. PRXs confer a protective antioxidant role in cells through their peroxidase activity in which hydrogen peroxide, peroxynitrate, and organic hydroperoxides are reduced and detoxified using reducing equivalents derived from either thioredoxin, glutathione, trypanothione and AhpF.	3.40268e-88
NZ_CP036280.1\|WP_145446181.1\|2255839_2256334_-\|transcriptional-repressor-NrdR	gnl\|CDD\|234774	PRK00464, nrdR, transcriptional repressor NrdR.	2.04353e-71
NZ_CP036280.1\|WP_145446170.1\|2243684_2244344_+\|glycerol-3-phosphate-1-O-acyltransferase-PlsY	gnl\|CDD\|234691	PRK00220, PRK00220, glycerol-3-phosphate 1-O-acyltransferase PlsY.	4.28236e-52
NZ_CP036280.1\|WP_145446182.1\|2256358_2257249_+\|YmdB-family-metallophosphoesterase	gnl\|CDD\|379099	pfam13277, YmdB, YmdB-like protein. This family of putative phosphoesterases contains the B. subtilis protein YmdB.	4.37043e-108
NZ_CP036280.1\|WP_145446178.1\|2252609_2253845_-\|glycosyltransferase	gnl\|CDD\|213815	TIGR03469, HpnB, hopene-associated glycosyltransferase HpnB. This family of genes include a glycosyl transferase, group 2 domain (pfam00535) which are responsible, generally for the transfer of nucleotide-diphosphate sugars to substrates such as polysaccharides and lipids. The genes of this family are often found in the same genetic locus with squalene-hopene cyclase genes, and are never associated with genes for the metabolism of phytoene. Indeed, the members of this family appear to never be found in a genome lacking squalene-hopene cyclase (SHC), although not all genomes encoding SHC have this glycosyl transferase. In the organism Zymomonas mobilis the linkage of this gene to hopanoid biosynthesis has been noted and the gene named HpnB. Hopanoids are known to feature polar glycosyl head groups in many organisms.	9.16541e-57
NZ_CP036280.1\|WP_145446185.1\|2259436_2260882_+\|dihydrolipoyl-dehydrogenase	gnl\|CDD\|235798	PRK06416, PRK06416, dihydrolipoamide dehydrogenase; Reviewed.	0
NZ_CP036280.1\|WP_145446167.1\|2241517_2242675_-\|biotin-synthase-BioB	gnl\|CDD\|273075	TIGR00433, biotin_synthase, biotin synthase. Catalyzes the last step of the biotin biosynthesis pathway. All members of the seed alignment are in the immediate gene neighborhood of a bioA gene. [Biosynthesis of cofactors, prosthetic groups, and carriers, Biotin].	1.28218e-144
NZ_CP036280.1\|WP_145446184.1\|2258397_2259279_-\|formyltetrahydrofolate-deformylase	gnl\|CDD\|235676	PRK06027, purU, formyltetrahydrofolate deformylase; Reviewed.	8.76319e-95

>NZ_CP036280.1|WP_145446174.1|2247696_2248995_+|histidine--tRNA-ligase
MSMKLQGPRGTRDFYPEAMAWRRRLEDAWRTVSVRHGFEEVDGPIFETQELYKIKSGDGILSEIFHVRHPQGDAEFAIRPEFTPTLARMVAARANGLPKPIKWFATPNFCRAERPQRGRLREFWQWNVDIIGAEGALADAECILVAVDLLREFGMTSQHVVVRISHREVVRQILLRLGVAEEKLTEAFELLDRREKMEHDAFVESATLLGLDGAKVERFLQMCRRRYPVGEIDHLARSIGMEEGFESLRELEEQLIGFGIGDWCAYDLGIVRGLAYYTGTVFELHEASGMERAVAGGGRYDKLIELFGGPKMSAVGFGMGDVVLTNVLQDKGLLPEDVTPQPDVFVLASSEAGAGSLRRVIADLREAGVHARFSYKSTTNVGKLLKEANQSRARFALLLGDAVSDGEGELKDLDTGDQQVVKLAGVADRLSV
>NZ_CP036280.1|WP_145446173.1|2246782_2247700_+|methyltransferase-domain-containing-protein
MSIPPPPPPRSSNKDKKGTSKKGSKGPTKAERADRYALYLKAVQDPDHEVEFFEQAYREANGSAEPLVLREDFCGTFAVCCKWVAGKAGRRSLGVDLDAEPLAWGKKHHLEKLTVEQQKRVTLVQDDVRKVCSPKADVLAAQNFSFYLFMERKELLAYFKAARRNLAPGGVMVLDMMGGPDCLLEDQNEPRKCDGFTYVWRTETVNPITNISEHSIGFKFKDGSKLERAFSYRWRLWSIPEVRDLLEEAGFARVDVYWEGEGDEGEGDGNWKITTEAAMDPSWLCYVVARRDHEAVTTVDHEGKA
>NZ_CP036280.1|WP_145446172.1|2246084_2246699_-|methyltransferase
MRVIAGSHKHRRLLGPPDAETTRPITDRVKQALFDRLTALGLLGDTLEQPFGPTLDLFAGTGSLGIEALSRGSTHCTFVEADRRIQSILRDNLEQLGLADRATIVHGSALLPLWIQNLPDTPVALVFLDPPYKLMDDPDAVERLLSLMAQLAPRLEPGGIINLRTPKQTPTPPEVDGLDGPVSLDYGSMTLHLYQTPLDDENDA
>NZ_CP036280.1|WP_145446171.1|2244450_2246088_+|2,3-bisphosphoglycerate-independent-phosphoglycerate-mutase
MSDSPKPVVVIVRDGWGRNPNPEHDAFNAVKLANTPRCDALLERYPSTLIHTSSEDVGLPEGTMGNSEVGHQNIGAGRVVDQESVRITKAIRDESFFANEALAGAVERAKTGRRYVHLMGIASDAGVHGLMTHLYACLELCKRMGHERVALHLFTDGRDTGPFTGKGYVEAIEAKCREIGVGQVASICGRYYAMDRDNRWERVAKAYSCLTGIHGRKNELPIAATAAEAIQNYYDSPTNDSQKGDEFIVPTMIGDSIDDALGTRISIEDSVIFYNYRGDRPREIVKAFTMSDEEWASVPPSPDTGANGFNRVRRLGVEMVTLTAYEEGLSVKVAYPKPPKMEDIGGAYLSRMGKTQFRCAETEKFPHVTFFCNDYREEPFEGESREMAQSPKVATYDLQPEMSAPRIKEIVLGRVAADDCEDFILVNFANGDMVGHTGSLEAAIKAVETVDGCVGEIVEAVVARGGKLIVTADHGNAEQMFDPNTNAPHTAHTLFDVECIVVDPSLDASVQLREGGRLADVMPTALALMGMEQPAAMTGVSLLEA
>NZ_CP036280.1|WP_145446170.1|2243684_2244344_+|glycerol-3-phosphate-1-O-acyltransferase-PlsY
MSVWIWMVLGYLCGSIPFGLLLGWARGVDIRRHGSGNIGATNAGRVLGRRMGLICFGLDLAKGLLPVLAFSLLGEREAGFWGALSGMGVAVSAMAGHILPVWLKFKGGKGVATGLGVMLGLWPVVTLPAVVAGVAWVGVTWFWGYVSLGSVVAAGLLPVLAVASGVSQGLSASEIGVYGVVTGALGVMVIVRHKGNMARIRSGTEPRVGWSRRGERPSA
>NZ_CP036280.1|WP_145446169.1|2243081_2243396_-|hypothetical-protein
MGRRTLGCLLAVNAMLLFGIAFTSFIPQPQPALAQNLGRGNYLMIAGDATGRSSQAALYIVNLSNSRVISGFFNASTNRFEFIAARDLTRDLAEAEAQRSRRTR
>NZ_CP036280.1|WP_145446168.1|2242718_2243051_-|hypothetical-protein
MNTSTDKLITRLACYFLIASGFVLSGFLLTQARDYVDNPAQAAMVINRDNLTLMTAKTRNGEESLFVLDNQNARLFVYRVDINRNQMNLVGLQDLNEIFSTSDDQPGRRR
>NZ_CP036280.1|WP_145446167.1|2241517_2242675_-|biotin-synthase-BioB
MISPSTPDNDQRIAEIATSVLAGNLVSREQAQFLASLEGDDLYDLFYWANKIRIRFVGRQVKFCSIVTGKTGACSEDCSYCSQSKHYKTHVTPDKMTVDEMLQATEEARANGANSMGIVNSGRGPTDRELDWLEPFYRKTAEQGTIRPCATLGELTPEQAQRLKDMGVQRINHNLETSARHFKNIVSTHDYKDRVQTIRNAKNAGLSICAGGIFGLGEDWDDRIDMALALRELDVDVVPINFLNAIQGTPLYGEVTRLEPMQALHIIAVYKFILPQQELKIAGGREKILRDLQSWIFFAGGSSFLIGNYLTTFGRTPQQDHQMLKDLGLTYTTFDEVEHEAQPDAAMTRSPGHDSPAREGALLSRRDGSLVALPVLNQGEKLVTT
>NZ_CP036280.1|WP_145446166.1|2240671_2241349_+|hypothetical-protein
MKRMLMSGLLAGLMTTGAMGADSDLLDISFVPTLDDGLEQIAAGRIRGWSTGWEAGTGLEVGVPGHANASWNWSSAVGAQSFVWELVDGVSTLSINGRMVMEGGLDQSVTDLSLQLRATDYRDYTGSLSATGLTLTVDGQAHSLPDLLAESGWSGLLRVGGLDGGGAPIRLEGTLTGNFHEIKEERIKIDMRAYHNPAAVPELPEPSTMLLGAAGIGFLLLRRGS
>NZ_CP036280.1|WP_145446165.1|2239972_2240455_-|D-tyrosyl-tRNA(Tyr)-deacylase
MRALIQRVRSASVAIDGKTTGAIQRGYAILLGVGHDDTPATAQRLADKIVNLRLFPDEQGRFDRSLLDINADALVVSQFTLYADARKGRRPSFLAAGKPPIAEPLCEHFCQCLRDLGVPSVQTGRFGADMLVSIENDGPVTLWLDSDELGISDNPPTKPE
>NZ_CP036280.1|WP_145446177.1|2251487_2252609_+|3-isopropylmalate-dehydrogenase
MSLNLAVIGGDGTGPEVVAQALRVLDQVAKDGGFEVQTTPLPYGGERYLETGTVLTDDEVEGLKAYDAILLGAVGHADVPPGVLEKGILLKLRFELDQYINLRPVKLYPGIETPLAGKGPDEIDMVVVRENTEDLYCGNGGVARRGTAQEISTQEMIATRFGVERCLRYAFELARSRKAQGFPGRLTLVHKTNVLTFCGGTWFRAFEAIGEADYADIEREYHHVDACCMYLATKPEIYDTVVVPNMFGDIITDLGAAIAGGMGIAASGNLNPDPSNPNPSMFEPVHGSSPDIAGQNKANPLACIDSLAMLLRETGRTQGKPALEAAGERVGAAVLAVTPKFTGKKLDRSGYGTSEIGDMVLEALGAIPVGASV
>NZ_CP036280.1|WP_145446178.1|2252609_2253845_-|glycosyltransferase
MTLLAALWWTWTLALAGATLLWLRVNTSDTHRSNTRYQVEPPAPDEDTDDNLPPVALLVPARNEAEHLPETLESLCRQNYPDLTLVFVDDDSTDDTAKLADQLAQRYPHLHVLHNQQAPPPGWVGKPHALYRGYQHLRQIEAAGAWQATWLCFTDADIHWHPDCLRAAIRHAQQHDADLVGLYPGLRFGTWVEAVVQTQLILALAVLFPVDKAMDPKVDETLIGGAFILTRRDNYDAIGGHEAVHNFVVEDLALGRRLKKNGARVRLAAARDLLWCRMYNGWLDLWEGLTKNAYAGLRYNPFRVTFLILCTFTFNILPALSIIPSAIAWYLTRDPAFAWPTLLALAANLLGTSALNASRIFARLPWHHALTLPVGSAIYLAIILASVRDYYFGGNHWKGRTYGTDVKKRGV
>NZ_CP036280.1|WP_145446179.1|2253891_2255160_-|methyltransferase
MPATDSRDRVLAAINHQQPDRLPIDFGATFITGLHCSVIEQLRQHYGLEQRPVRVHEPYQMLGYVEDDLKAALGIDTQGVIPHSTMFGFPATGWKSWTTPWKQDVLVPADFVTTTTDKGDVYIYPQGDSDAHASGHMPAGGYFFDAIVRQEPIDEDNLAVEDNTEEFKPLTDDELQTITRGVRDAHATGRAVVVCSPGTGLGDIALVPAPFLKQPKGIRDISEWYMSTAMRPDFVRAIFRHQVDIALPNLQRLNDEVGDLIDVIVICGTDFGTQTSQFCSVDTFRDLWLPFYREINDWVHANTRWKTFKHSCGAVAGLIDSFIDAGFDILNPVQCSATGMDPAELKAGFGKRITFWGGGIDTQHVLPFGTPTEVREQVTDRCRIFAQGGGFVFNTIHNTQAMTPVDNFVAMVDAVHTFNKNA
>NZ_CP036280.1|WP_145446180.1|2255228_2255666_-|CBS-domain-containing-protein
MPNVQLLLDRKGNKVHSVPPETTVDRAAEIMNEHNIGSLLVVDDENLKGIITERDILRKVIAAGRKPETTSVKSVMTDNLWTCTPETSLEDISDIFKDRRVRHLPVVTDAGELAGVISIGDLNAFRLEGQAVMIEYLHQYIHGAA
>NZ_CP036280.1|WP_145446181.1|2255839_2256334_-|transcriptional-repressor-NrdR
MRCPYCEANKDRVIDSRPAENGKAIRRRRECLNCSKRFTTYETVEETTKLVVVKRDRSRVPFDKAKMLAGLEAACYKRPVPTRRLQEAVDHVTEELRRTGQREIDAEDIGQRLAEQLRTIDQVAYVRFASVYKQFRDLDDLIEEVRGVLEMNERLSPGQGKLFR
>NZ_CP036280.1|WP_145446182.1|2256358_2257249_+|YmdB-family-metallophosphoesterase
MEVLPVTGGSVRIRIAILGDIVGTPGRQVVASAVKRLKREMGVQVVIANVENAANGSGLTPDLHKKLQLAGLDGMTMGDHAYRKKQIVPTLERGSDIIRPANLSAKAKGKVCLRLVAEVEEVKLPIYVFTVVGRLFMNTMQGTDPFATADRLIEQIHERPSVILVEVHAEATSEKVAMGWYLNERVTAVFGTHTHIQTADARVLPREIEGPRSGASVLPLGEGGTAYITDLGMSGPQDSVLGRRVDRVVSQMTTAMPAAFDVAEGNPEARGVIVEVESSTGRAVGVETIVLGPEDA
>NZ_CP036280.1|WP_145446183.1|2257391_2258393_+|diguanylate-cyclase
MEERENRRVTADLSDGLRLTDELSVDELSLPEVAWPRHGLTTTLRGILTGGVVAAGVAGGLGWWLGGPLLSAAAVAGVAGYAHWRLSRGVVQSLGNLIDRLELTSCNPTSELVEKLPLEREDEIGQVARAMARVCRNSIRKGFEAQQLRRTIDQRVRLATRKATSRLQRETLRDPMTDLGNRRFLEEQGPKLFDATEASDLSLLCVAIDLDHFKAVNDTLGHAAGDDVLVFVGSLIKATTREDDMAVRLGGDEFLVLMPGADFDRGLKFAAQLRSLFTQQTGLLTRGGPKPDLSIGIAERLSDRCDSLQSLMERADERLYTAKRNGRGRAEAG
>NZ_CP036280.1|WP_145446184.1|2258397_2259279_-|formyltetrahydrofolate-deformylase
MPEIKAVVSVIGRDQKGVVARFATYLAERGVNILDLEQQVVNGEFIMDMLVDLADMTPSLDQLITDLLELGRDIEMEVRVALHDRKPKRVAVLVSKEAHCLQTLIDDWKAGKFRGDLVTVLGNHPDLEPVAKAAGLPFAHFPAKPDKQAHFKWMMEQLAKAQPDLIVLARYMQIVPPEMVQAFRYKIINIHPSLLPHFPGAKPYHAAWEAGVRVAGCTAHFVTEDLDEGPIILQDVFHIDVGRDTAEDVRANGQRLEGRILADAVQMFLDQKLVVVDDKVVFRPGLSSMLDHA
>NZ_CP036280.1|WP_145446185.1|2259436_2260882_+|dihydrolipoyl-dehydrogenase
MSETATYDLVVIGGGPGGYVAAIRAAQLGMKVACVERDRLGGVCLNWGCIPTKALIAGAEFYHRLTHEAEEWGVKAEGVTHDWGRVIERSREVAGQLNKGVGFLLKKNKVTHIEGHAFIPSAGKVEIYASDDSERQGSVKQVLEAGKILIATGARPRPLPGAEFDGKRIIGAKEAMTLTEQPKSMVIVGAGAIGMEFAYVYNAYGTRCTVVEMMDRVLPIEDTEASDVVERAFGKMGVTVKTGHKTLSLEKTDEGVRATVAPADDESKTEVLEADVVLVAIGVMGRYDGLFDASLGVETFKDHIKVDYRSAGADYQTSVPGIYAIGDVIGPPWLAHVSSEEGIVCVERMAGHEVEDIDYDAIPGCTYCQPQVASVGLTERACEEQGIEYVASKFPFAASGKAQALGATEGFCKLISGKKHGEVLGAHMVGEGVTELIAEIGLAIKLEATMDEVIGTMHAHPTLSEATHEAALGAQNRMIHF
>NZ_CP036280.1|WP_145447261.1|2260942_2261548_+|redoxin-domain-containing-protein
MVMTASTMLGLGTQAPDFSLPDTEGGTVSRSDFAGKPLLVVFMCNHCPFVKHVARQLKALGDDYMPKGVAMVGISANDVSTHPDDSPENMKSEKAARGYAFPYLYDADQSVAKAYTAACTPDVFLFDAEHNLVYRGQLDETRPKRLDSGAYDYDHPASDGKDLRAALDTMLNGGSIPAEQTPSMGCNIKWKAGSEPSYFGG

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Crispr_ID: NZ_CP036280_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_6

2849542-2849659

Orphan

Consensus_repeat	Method
CGTCGACCTGCTCGACCTCTCCATCCTCGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036280_6

>merge|NZ_CP036280|6|2849542-2849659|CRISPRCasFinder
CGTCGACCTGCTCGACCTCTCCATCCTCGCCAGCCACTTCGGGCAATCAGGGGACTGGGCTCAGGGCAGTTTCAACGGCGACGGGGTCGTCGATCTGCTCGACCTCTCCATCCTCGCC

>NZ_CP036280|6|6|2849542-2849659|CRISPRCasFinder
CGTCGACCTGCTCGACCTCTCCATCCTCGCC	AGCCACTTCGGGCAATCAGGGGACTGGGCTCAGGGCAGTTTCAACGGCGACGGGGT
CGTCGATCTGCTCGACCTCTCCATCCTCGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145446684.1\|2845120_2845906_-\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP036280.1\|WP_145446689.1\|2852560_2853316_-\|PEP-CTERM-sorting-domain-containing-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446688.1\|2850476_2852465_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|225914
NZ_CP036280.1\|WP_145446692.1\|2855657_2856917_+\|trypsin-like-serine-protease	unknown	unknown	gnl\|CDD\|238113
NZ_CP036280.1\|WP_145446685.1\|2845808_2847587_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237425
NZ_CP036280.1\|WP_145446691.1\|2854725_2855634_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|225076
NZ_CP036280.1\|WP_145446695.1\|2859627_2860728_+\|PDZ-domain-containing-protein	unknown	unknown	gnl\|CDD\|273938
NZ_CP036280.1\|WP_145446694.1\|2858250_2859555_+\|DUF1343-domain-containing-protein	unknown	unknown	gnl\|CDD\|377768
NZ_CP036280.1\|WP_145446671.1\|2833711_2834134_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP036280.1\|WP_145446690.1\|2853633_2854686_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271213
NZ_CP036280.1\|WP_145446680.1\|2839572_2840364_-\|DUF429-domain-containing-protein	unknown	unknown	gnl\|CDD\|377266
NZ_CP036280.1\|WP_145446678.1\|2838043_2839498_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270303
NZ_CP036280.1\|WP_145446673.1\|2834175_2835282_-\|3-dehydroquinate-synthase	unknown	unknown	gnl\|CDD\|341474
NZ_CP036280.1\|WP_145446682.1\|2843978_2844800_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225360
NZ_CP036280.1\|WP_145446693.1\|2857195_2858212_+\|phenylalanine--tRNA-ligase-subunit-alpha	unknown	unknown	gnl\|CDD\|234780
NZ_CP036280.1\|WP_145446676.1\|2837046_2838033_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379313
NZ_CP036280.1\|WP_145446674.1\|2835394_2836999_+\|glutamine-hydrolyzing-GMP-synthase	unknown	unknown	gnl\|CDD\|234614
NZ_CP036280.1\|WP_145446687.1\|2849733_2850399_-\|SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|366722
NZ_CP036280.1\|WP_145446669.1\|2832803_2833709_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237171
NZ_CP036280.1\|WP_145447304.1\|2860728_2861358_-\|superoxide-dismutase	unknown	unknown	gnl\|CDD\|223678

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145446684.1\|2845120_2845906_-\|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].	8.12571e-56
NZ_CP036280.1\|WP_145446688.1\|2850476_2852465_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|225914	COG3379, COG3379, Uncharacterized conserved protein [Function unknown].	4.29631e-20
NZ_CP036280.1\|WP_145446692.1\|2855657_2856917_+\|trypsin-like-serine-protease	gnl\|CDD\|238113	cd00190, Tryp_SPc, Trypsin-like serine protease; Many of these are synthesized as inactive precursor zymogens that are cleaved during limited proteolysis to generate their active forms. Alignment contains also inactive enzymes that have substitutions of the catalytic triad residues.	9.98953e-14
NZ_CP036280.1\|WP_145446685.1\|2845808_2847587_+\|hypothetical-protein	gnl\|CDD\|237425	PRK13557, PRK13557, histidine kinase; Provisional.	4.8053e-41
NZ_CP036280.1\|WP_145446691.1\|2854725_2855634_+\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|225076	COG2165, PulG, Type II secretory pathway, pseudopilin PulG [Cell motility and secretion / Intracellular trafficking and secretion].	4.96479e-10
NZ_CP036280.1\|WP_145446695.1\|2859627_2860728_+\|PDZ-domain-containing-protein	gnl\|CDD\|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	5.00991e-86
NZ_CP036280.1\|WP_145446694.1\|2858250_2859555_+\|DUF1343-domain-containing-protein	gnl\|CDD\|377768	pfam07075, DUF1343, Protein of unknown function (DUF1343). This family consists of several hypothetical bacterial proteins of around 400 residues in length. The function of this family is unknown.	1.08077e-162
NZ_CP036280.1\|WP_145446671.1\|2833711_2834134_-\|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.	3.29786e-17
NZ_CP036280.1\|WP_145446690.1\|2853633_2854686_+\|hypothetical-protein	gnl\|CDD\|271213	cd14254, Dockerin_II, Type II dockerin repeat domain. Bacterial cohesin domains bind to a complementary protein domain named dockerin, and this interaction is required for the formation of the cellulosome, a cellulose-degrading complex. The cellulosome consists of scaffoldin, a noncatalytic scaffolding polypeptide, that comprises repeating cohesion modules and a single carbohydrate-binding module (CBM). Specific calcium-dependent interactions between cohesins and dockerins appear to be essential for cellulosome assembly. This subfamily represents type II dockerins, which are responsible for mediating attachment of the cellulosome complex to the bacterial cell wall.	4.05394e-11
NZ_CP036280.1\|WP_145446680.1\|2839572_2840364_-\|DUF429-domain-containing-protein	gnl\|CDD\|377266	pfam04250, DUF429, Protein of unknown function (DUF429).	2.97168e-05
NZ_CP036280.1\|WP_145446678.1\|2838043_2839498_-\|extracellular-solute-binding-protein	gnl\|CDD\|270303	cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.94206e-27
NZ_CP036280.1\|WP_145446673.1\|2834175_2835282_-\|3-dehydroquinate-synthase	gnl\|CDD\|341474	cd08195, DHQS, Dehydroquinate synthase (DHQS) catalyzes the conversion of DAHP to DHQ in shikimate pathway for aromatic compounds synthesis. Dehydroquinate synthase (DHQS) catalyzes the conversion of 3-deoxy-D-arabino-heptulosonate-7-phosphate (DAHP) to dehydroquinate (DHQ) in the second step of the shikimate pathway. This pathway, which involves seven sequential enzymatic steps in the conversion of erythrose 4-phosphate and phosphoenolpyruvate into chorismate for subsequent synthesis of aromatic compounds, is found in bacteria, microbial eukaryotes, and plants, but not in mammals. Therefore, enzymes of this pathway are attractive targets for the development of non-toxic antimicrobial compounds, herbicides and anti-parasitic agents. The activity of DHQS requires nicotinamide adenine dinucleotide (NAD) as cofactor. A single active site in DHQS catalyzes five sequential reactions involving alcohol oxidation, phosphate elimination, carbonyl reduction, ring opening, and intramolecular aldol condensation. The binding of substrates and ligands induces domain conformational changes. In some fungi and protozoa, this domain is fused with the other four domains in shikimate pathway and forms a penta-domain AROM protein, which catalyzes steps 2-6 in the shikimate pathway.	7.69496e-163
NZ_CP036280.1\|WP_145446682.1\|2843978_2844800_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|225360	COG2771, CsgD, DNA-binding HTH domain-containing proteins [Transcription].	6.56527e-09
NZ_CP036280.1\|WP_145446693.1\|2857195_2858212_+\|phenylalanine--tRNA-ligase-subunit-alpha	gnl\|CDD\|234780	PRK00488, pheS, phenylalanyl-tRNA synthetase subunit alpha; Validated.	0
NZ_CP036280.1\|WP_145446676.1\|2837046_2838033_+\|hypothetical-protein	gnl\|CDD\|379313	pfam13650, Asp_protease_2, Aspartyl protease. This family consists of predicted aspartic proteases, typically from 180 to 230 amino acids in length, in MEROPS clan AA. This model describes the well-conserved 121-residue C-terminal region. The poorly conserved, variable length N-terminal region usually contains a predicted transmembrane helix.	1.63438e-08
NZ_CP036280.1\|WP_145446674.1\|2835394_2836999_+\|glutamine-hydrolyzing-GMP-synthase	gnl\|CDD\|234614	PRK00074, guaA, GMP synthase; Reviewed.	0
NZ_CP036280.1\|WP_145446687.1\|2849733_2850399_-\|SAM-dependent-methyltransferase	gnl\|CDD\|366722	pfam01596, Methyltransf_3, O-methyltransferase. Members of this family are O-methyltransferases. The family includes catechol o-methyltransferase, caffeoyl-CoA O-methyltransferase and a family of bacterial O-methyltransferases that may be involved in antibiotic production.	3.18903e-59
NZ_CP036280.1\|WP_145446669.1\|2832803_2833709_-\|hypothetical-protein	gnl\|CDD\|237171	PRK12678, PRK12678, transcription termination factor Rho; Provisional.	0.000168515
NZ_CP036280.1\|WP_145447304.1\|2860728_2861358_-\|superoxide-dismutase	gnl\|CDD\|223678	COG0605, SodA, Superoxide dismutase [Inorganic ion transport and metabolism].	5.91872e-87

>NZ_CP036280.1|WP_145446685.1|2845808_2847587_+|hypothetical-protein
MSPGSSPAATSGLFSSPAANVWGWNCFQSLPGITGFFAIYLVLHGLATHAALLLQYGVDKGTGDISMMWVPTGILGPALALIRPRLWPLLLAGAGLTEYAVAWSGTIGTPAATDGHFLSFLTIATLGNLMTATCFATCFRWMSPHANPMMSTRDFTLYILVAIGVVTIFTSTLTTGLIDLNNRLHDMPYNWLLAWQQWWMSDLTTLMVLATPILLLGTVEYERVMSPIRWLEALTLLGLEAVYFGWHFQQSRGSYPLYHAWITIMIVFHLWAVTRFNALMLSLANVIIAVSAFSSASGNSALWDSMTDDPVGKALYIQGFVLGWTLMMGFIMAIFEDRRRAHARELEAEKQLRALDRVEALGTMSAGVAHDFGNLILAIRAYESTIRANITNPSESLQKAMQGLGESAATAQTLIQALLHFGRQDPSDEETGSTDLTHTVQTTCEALTPLIAVKCALRCGIPTGSIIVPISHNNLERVLRNLILNARDAARGQGRIEMRIVLRDQTVDVLVRDNGTGIPADKLDKIFDPFFTTKARGKGTGLGLSVVMGLIQEAGGSVRAESVEGEGTTITLTLPVLETTLSEGCAAESKCC
>NZ_CP036280.1|WP_145446684.1|2845120_2845906_-|response-regulator
MPGRLWKQFQPQTLAAGEEKSPDVAAGLEPGLMNDLSCDYGGVRSKWVNRPNSIVIVDDHRLVAEGISSLLETVPDLEVVAHVYDPAEIISKIRDHKPDIVLCDLDMPGGDPLDSASQAIESLPDTRLLILSAYPTDVNIERALKIGVAGFITKNESAETIVDGLHAVAAGHAIYSDEVRQRFVNRTDRPDNAPAILALSPRELTVTLLAAQGMTTPQIAKTVYRSTKTVDKQISSAMAKTGCTNRVDLSRWAIREGLMRA
>NZ_CP036280.1|WP_145446682.1|2843978_2844800_-|helix-turn-helix-transcriptional-regulator
MSGVGQSVITYLSDKDPMSSDSLKYLDSTQHAVIVQVLEMVRQQLGAHWGYAHTTLPGLPAEGTVATGLSPEIARTLNLSQWHTDEGSLIRYCMGEAEHHDQVIRPLALRGISPMVQAALFRRFTRHRQLGDVLAAVISLSGHHAITVVFARWAGANSFVESDERVMEGLIRRLPARLTQARAASAAPPRVLTKVNGRRALTNTESVVLDYLRQSLTEVQIANELSRSPHTVHVHVKSIYLKYGVSSRKELLARLQAQELQAEAPGGASSISG
>NZ_CP036280.1|WP_145446680.1|2839572_2840364_-|DUF429-domain-containing-protein
MLNSILGIDFSAARDAGRRIWITRAHINDDALRILEVSDLASLLSVTPSPDDCLPALVDSLCQQPPAIIGIDAPLSVPLRFMPDGYERFVRDCDLTADQLREQIRDEKRKCDTEASTPFAPGNLRMYRQTHAVITRVIRPLVKRHAASVQPMMDASHDQHVLIEACPASSLRTAGRVGELELRPYKGRSAEHRKQRAVILDWLMTKRVLDVPDRLRRRLLDNSGGDALDSLICAVITACARRDLNSPCADHHEREGRVFFKLD
>NZ_CP036280.1|WP_145446678.1|2838043_2839498_-|extracellular-solute-binding-protein
MSQSNLTERLTALISLPRDLLVGLVQSIEHISTGTRVIVVIGLITTIAVWFWPIPQRPGIEFWVFADIHEQMYRPVVEAWNEDRPGASRDEQIHIFMIGADPMVRRALAGFWSDTPVAAMMEIAESYSGLFFSGPLDEIGFVDLTDRLKEEGIYEQINEASFSPWTSRGRIFGLPHDVHPVLLGYRADIVEAAGIDVSTIETWEDFIRVMSPLISDLDGDGITDRYLLDFWYTSTPHIYALCLQAGGGTFDQQERLILDSEANARVAATLVTWCLGEDRIMIDASHTNASGHVIKTRGHVVATLMPDWLAGAYITQFPQFHGKMKIMPLPAWDPGGRRASVMGGTMLAINKASEHKEVCWEFAKEIYLSEACARSLFESVHIISPVKSLWDKPFYRKRFDYFSGQRSGLLYIEHAEEVPLRTSSPFNQMAIDELGIAVSAVYRHAVARGIDDVDALLPVAREQMRLAEERVAHEMRRNVFVTQP
>NZ_CP036280.1|WP_145446676.1|2837046_2838033_+|hypothetical-protein
MDRPRTWMFLGLLTLLIAGCGLTPESQDQKHVEAASLKQPVAVNLIRDKMYFRAPVEVNGEPMGSFLIDTGAAMAAMDLGLVRRLELPVNGDGRAIGIAGTESFNYHRVESLAVGGVGLKAKRIAGMNMYKLHRHRRQRLDGILGYPTLAEVPFALDGPDRTLTFYPRRTFRAPDDANPVRLIRFRNLPTVEATIGNGHRIWLVLDTGSDEMLSLPDDLPARWPDVLSVDVSGMSRNLGVGGMVHGRTGWVSSINVFGHRFKDVEANFAPPPSSFKGAPVPVGRIGNGVLRRFCLTFDRQRNRMWAELDQTLVKQSDSDTTVGTTSSP
>NZ_CP036280.1|WP_145446674.1|2835394_2836999_+|glutamine-hydrolyzing-GMP-synthase
MSTPASTTATQALAEVPESLYGEVIPIVDFGSQYVQLIARRVREAGVYSVLVSPETPIEDLRRIRPKGIILSGGPSSVYDEGAPRCDPALFDLGVPVLGICYGMQIGCELLGAKVASAEAREYGRARLRVTTTSDNELFKGMPDETSVWMSHADQVRELSEDFIPVATTETCPYAAVRHRERAFYGLQFHPEVTHTPHGAEILSNFIFGVCGCSGTWQMSNFLEMSIEQIQAQVGDGRVICGLSGGVDSSVAAALLHRAIGPRLTCVFVDNGLLRKGERAFVEATFRDHFDIDLRVIDAGAQFLADLEGVLDPQEKRRRIGHRFIKVFKSASEEIEDVGFLAQGTLYPDVIESGQGHSGQAANIKLHHNVGGLPEQLGFDLVEPFRQLFKDEVRQLGSLLGLPETMVWRHPFPGPGLAVRCLGEVREDQLAILREADEILIEEIVANNLYRQTAQVFAVLLPVRAVGVMGDGRTHEQVIAIRAVESQDFMTADWARIPFDVLATISNRVINEVRGVNRVVYDISSKPPATIEWE
>NZ_CP036280.1|WP_145446673.1|2834175_2835282_-|3-dehydroquinate-synthase
MATVDLQLPPTAHGYDIRIEPGLLDSLGEMVREVAPHHKAALIVDEAIEVDVGKPAAKSLQNEGFETTVAVMTPTEKKKTLGTVRSLYEVLLEARIERRSPVIALGGGITGDTAGFVAASYLRGVPFIQCPTTLLAMVDASVGGKTGVNTTHGKNLIGAFHQPHRVIIDVSTLESLPERELRCGLAECVKHGVIRDPGLFTWIGEHADRILQLDHGTLVELVERNVRIKAAVVEEDEKESGVRAHLNFGHTFAHAIEAASAYGRIKHGEAVALGMVAATRMAIAMKICHPSLEHQVVDLLEALGLPTWEDDLPVTALLMKVMAIDKKVADSRIRFVLPTKLGEVIITSDPTPELVAEAWDSLRVDPRA
>NZ_CP036280.1|WP_145446671.1|2833711_2834134_-|biopolymer-transporter-ExbD
MSRRSVTDLAPRVELLPLIDVIFLLLTYFIYSMTVMVHAELMPVELTPLEHGQAAESQPALSITLDRDGELFINREPIRLSDLAQNIADRLEEDPEMRVFLALEEDETTTTDRGPLLIRVVETLRQAGVQDLAVVGGQGN
>NZ_CP036280.1|WP_145446669.1|2832803_2833709_-|hypothetical-protein
MSVLARPTASQDFGTFGVTLILSVLLHLLIIMGMYQDASVVLERDTLRPRDQKTRIEPGDTPPSTARVAWIAREDYQAIMARQSTTEQPALQATADPTPDAQANPLPTSPENNTPSDQTTPLSQSVPVPPTDQTAQPEASGDTLPRNEQTPLPEPAPPQNTPPSSTATAGEPGPENPTSLPKDEREAPPTRIEREIAVKPGNRVEARQGLVIQTRLPRFTVAARAVLPQRNPVVIITFNTDGQVIHVDWIRKSGHALHDSPIESSLYQWEASGPLLERAESPIEVEMKILLLRESRGSSED
>NZ_CP036280.1|WP_145446687.1|2849733_2850399_-|SAM-dependent-methyltransferase
MKNKTIENIGALYDYVVATSLRVAPAIRELMERTGEHEHAEMATDPTQCQFLAFLIRSIAAKRVLEVGVFTGVGTCWMADAVGPDGKVVACDVSEEFPAIGRPYWEKAGLAGRIDLRVAPAAETLASLAETEGLGTFDFCYIDADKTAYDTYYELVLPLMRDGGVIALDNMLSDGSVANPQPGDARAVALDALNRKLHTDDRVDVSFLPICDGLYLVRKRP
>NZ_CP036280.1|WP_145446688.1|2850476_2852465_-|tetratricopeptide-repeat-protein
MTESKPRVLLIGWDAADWRFVDPLIDRGLMPTLASLRERGAWGKIATLQPMLSPMLWTSIATGKAARHHGICGFTEPLPDGSGIRPVSSVSRRCQAVWNILTQKQLRSHVVGWYASHPAEPINGTMVSNQFELPVGPAEQPWPVPPGAVHPADLSDVLAPLRVHPGEMDANAVLPLIPNAARDQQREGHRLGKAQSLLAQTVSIHTVATHLMMQDDWDFMAVYYEGIDRFAHEFMEFHPPRMDHVSDEDFENYQHVMTGVYRFHDMMLETLLKLAGEGTTVILMSDHGYLDDASRPNPDHAGPVDWHRPLGMVCVAGPSIKRGTRLFGPTLLDVTPTILRLFDLPVGADMPGRAWVEAMEDPTEPGRILSWESPSEDDGRHPADVQEDPESARAALQQLIDLGYVDPPGEDVAQTVADTRAHNDLTLARSMLSMGDTAEALEVLESLPTGFRNDAGIRAAIAQARLLCGDLEGCKAELDALADEPNSQGQRYLLLGAMSLRQGEDRRALEHYETARTHAPDNPALLSRLAGLQLRLGRPEKAAALYRQAIERAPEDATSWDGLAEAHLRLGENKQALDAALEAVGLAFGLARAHLRLSKALLAVGDTERAAEAVEACLIRSHGFVEAHEHAVAVYETLGDTDRANEHRRLADKARVARSSGS
>NZ_CP036280.1|WP_145446689.1|2852560_2853316_-|PEP-CTERM-sorting-domain-containing-protein
MHERARLWRHYRGGPVPWPRFACATCLRHPVPLAARPPATDREEKSMTRHESTDHRLLAYSLAAGAAALGVSDASAGIVYSGPQDIEVFQFGGQQLNLDGDAYDDILLKNYVFGGGNYQGLYVNFYPGKVNGFISGFAYASALSAGDPINAGTVSVFQASMAYGTNNPNAEFNNADGAFIGIGFPIAGVNHFGWIRVTIDNAAGRFIINDWAYEDQPGVGIAAGAGIPEPSALGLLAAGALGLAGYRGRRA
>NZ_CP036280.1|WP_145446690.1|2853633_2854686_+|hypothetical-protein
MTITAGTASAEIDHVVLDTPIVVQPGFTQQLELDGLPIFDPEDPANEGVAPPFDIFVNHWFAPDFTTYYEVNIRAFPGTVLVNGQSETVTYFPGTGSEQTQTYNLLDKLDIGQAIGPQTVGQIGSEFRGVLALNGAGAGEFYVPNGQSVTGMVGLSFVGIDSPPDERENRRVNYAWVEFTINAAPAGTGLGELVINQWAYETEYGRPILAGETSISLQKGDFDASGDLGQGDLDYMLSILGNNPLGEDDFNDDGAITMDDVDLWIVEALGSTAGDANFDGSVDLLDLSLLASNFDTPSGASWGDGDFNFDGAVNLLDLSALASNFETSPAPEPTTALLSLLGLAAIARRR
>NZ_CP036280.1|WP_145446691.1|2854725_2855634_+|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MLPTDRRKAGFTLIELLVVISIIALLIGILLPALGAARNTARQVQCLSNQRQVAVAYNLYAMDYRDSMIMPTSPFTNGPFVSPNYAYGSAQVDIYSSDRGNFNTGTPGGTYIWNLGGASGNGMLYELNYITDLEFFFCPDPPVTDLTNTFFAPVSDNTPRQVDSVDEDFGTQNWGSLGFGSARVGVGTFGNRSEMITNDDRSRAASANNISERQVYFGSLRFSDNANLAVSYCPIQISENESLPGAHNDRGMNATYGDGSGTFLAFADPYTREDIIDLEKFYSWLDSRGATLNNYFPSLEND
>NZ_CP036280.1|WP_145446692.1|2855657_2856917_+|trypsin-like-serine-protease
MFRHAGMGITACLLITTASDGVTFRHDRSVPDAAGLAASPAYESAGEIIINYFFGIPGQASGVLIHPEWLLTAAHPLTAVSIQSIDLTFTDQDTGQTVTAQAEEWIPYPQFNPLASIFNLDIGLVKLTEPLDNITPSPIYRDDGGERDQTITIVGYGNLGNGTSGGVLAAGGTAHAVTNTVDAFGGEPAGLYNLNAYEPSVMFMDFDPAPGVSELNHTGSATPLDMEGLSASGDSGGPGFIDVDGVPHVAGVVSVGLSRDSRFSAYGDLSGLTRVSAFTDWIDAHVPLGLPGDVDGDGALTAADIDLITAGFGSSDPILDLDQNGSVGASDIDAWLALAGSKRGDANLDTAVDLLDLSILAAHFDSTGTWADGDFNGDTSIDLLDLSSMASNFNTPATIPEPAAGLLLLGSIAVTPRRS
>NZ_CP036280.1|WP_145446693.1|2857195_2858212_+|phenylalanine--tRNA-ligase-subunit-alpha
MIERINELEQRATLDLEAVSDAESLEQFRIQYLGAKGELKALMGLMKEVPGDQKRAFGQGANALKQKVQQAYDERKASLGSNAKPSGPIIDITEPPAPPQRGRQHVITQTVSELTSIFGRMGFDVATGPEVEDDYHNFVALNIPDEHPARDPADNFYLDVPGGHKGQPGGPALLRSQTSTVQIRVMEKAQPPLRIISPGRVYRPDEHDATHYSMFHQIEGLYVDKGVTMVDLKTTLVQFAQAFWGPDADIKLVPSYFPFTEPSAELYVKIDLGKGVEWMEVGGCGMVDPAVFEHVGYDPEQWTGFAFGLGIERLAMRKHQIPDIRLLFENDVRFLRQF
>NZ_CP036280.1|WP_145446694.1|2858250_2859555_+|DUF1343-domain-containing-protein
MMPCSTSVLRSLAVLLLTGVAGCHAAAPADQQPVTKPEPVATRATAAEPVILGIDTLEADNFALLRGKRVGIVANPASVNRELRSTVDVLHQNQDKGGYQLVALYGPEHGVWGDVYAGDKIENQDDPRTGLPVFSLYGKTRKPTPEMLESIDILLFDLQDIGSRSYTYISTMSVCLEACAENGKQFAVLDRPNPLGGERIEGTMVEEGFYSFISHLDVPYLHGMTMGELAQLERDKLAPDYEGLTVVPMSGWKRSMVWEDTGLKWVPTSPHVPFASSTYAYAATGVIGELMVLSNGVGYTLPFEVVGDTGVDADQLADHMRATPLAIEGVTYRPARFRPFYATHKGEVLGGVQVYLDPRADSLYEVNFLLLDALDAKTQLSEGSKRHGMFDKANGTDDVRLWIEQGKPLAELFAQWRETSERFRETRKPFLLYD
>NZ_CP036280.1|WP_145446695.1|2859627_2860728_+|PDZ-domain-containing-protein
MRHNRWIPSALILSLATGLLLGSWWSSLAGPAIAQENATPDQGYLTSDEQRTIEVFERSREAVVFINTLGRRRDIFSRRVFEVREGSGSGFFWDNQGHIVTNYHVLHNATGAEIILDDQTRVRAQLVGVSRSHDLAVLKIDDPDINREALPHGDSARIRVGQTVLAIGNPFGLDHTLTRGVVSALNREIKALNGRTIGGVIQTDAAVNPGSSGGPLLDSSGRVIGVNTAILSPAGTSAGIAFAVPMATVQRVVPQLIESGNYTPPRMGVRFHDPTSQATLSRLGLQGALIIEVEPGSPAEKAGLRGTTRKFLGGINLGDVILAVDGQSVRDSNDLLQILETKAPGDTIHLTIWRNETRIAVEVTLK
>NZ_CP036280.1|WP_145447304.1|2860728_2861358_-|superoxide-dismutase
MPGYDSRSGQYVLPPLPYAYNALDAAIDEQTMRLHHDLHHAGYVRGLNGALAKLAEARESGDYAMVQHWSRKVSFNGGGHTLHTIFWSNMAPPSQGGGGEPEGALRDKIETDFGSVTKFKEHFSAAAGAVEGSGWGILGHDATSGKLIVVQGENQQKLTTWGITPVLVLDVWEHAYYLRYQNRRKEYIKNWWQVVNWSDVASRVSWHKA

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Crispr_ID: NZ_CP036280_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_7

2933858-2933973

Orphan

Consensus_repeat	Method
TCAACCTCCTCGACCTCTCCATACTCGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036280_7

>merge|NZ_CP036280|7|2933858-2933973|CRISPRCasFinder
TCAACCTCCTCGACCTCTCCATACTCGCCGCCAACTTCGACCAGCCCGGCTCCTACGCCCAAGGCGACCTCAACCTCGACGCCTCCATCAACCTCCTCGACCTCTCCATCCTCGCC

>NZ_CP036280|7|7|2933858-2933973|CRISPRCasFinder
TCAACCTCCTCGACCTCTCCATACTCGCC	GCCAACTTCGACCAGCCCGGCTCCTACGCCCAAGGCGACCTCAACCTCGACGCCTCCA
TCAACCTCCTCGACCTCTCCATCCTCGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145446760.1\|2938734_2939355_+\|transcriptional-repressor-LexA	unknown	unknown	gnl\|CDD\|234688
NZ_CP036280.1\|WP_145446763.1\|2943162_2944656_-\|glycosyl-hydrolase	unknown	unknown	gnl\|CDD\|350121
NZ_CP036280.1\|WP_145446746.1\|2920532_2921024_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP036280.1\|WP_145446752.1\|2926855_2927767_+\|D-amino-acid-aminotransferase	unknown	unknown	gnl\|CDD\|238799
NZ_CP036280.1\|WP_145446758.1\|2935520_2936126_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446754.1\|2930768_2931161_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446762.1\|2940383_2942810_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224276
NZ_CP036280.1\|WP_145446748.1\|2922031_2922985_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|223200
NZ_CP036280.1\|WP_145446757.1\|2934577_2935405_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446750.1\|2923972_2925679_+\|4-alpha-glucanotransferase	unknown	unknown	gnl\|CDD\|237738
NZ_CP036280.1\|WP_145446753.1\|2928224_2930618_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446749.1\|2923209_2924094_+\|acyl-CoA-desaturase	unknown	unknown	gnl\|CDD\|224316
NZ_CP036280.1\|WP_145446761.1\|2939405_2940413_+\|UDP-2,3-diacylglucosamine-diphosphatase-LpxI	unknown	unknown	gnl\|CDD\|377632
NZ_CP036280.1\|WP_145446755.1\|2931419_2932541_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446764.1\|2944749_2945475_+\|HAD-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|368291
NZ_CP036280.1\|WP_145446759.1\|2936551_2937730_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|271213
NZ_CP036280.1\|WP_145446765.1\|2946830_2947202_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446747.1\|2921118_2922054_+\|DUF3891-family-protein	unknown	unknown	gnl\|CDD\|379025
NZ_CP036280.1\|WP_145447308.1\|2945534_2946800_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340830
NZ_CP036280.1\|WP_145446751.1\|2925703_2926744_-\|DUF1611-domain-containing-protein	unknown	unknown	gnl\|CDD\|225902

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145446760.1\|2938734_2939355_+\|transcriptional-repressor-LexA	gnl\|CDD\|234688	PRK00215, PRK00215, transcriptional repressor LexA.	2.78587e-73
NZ_CP036280.1\|WP_145446746.1\|2920532_2921024_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	5.21143e-21
NZ_CP036280.1\|WP_145446752.1\|2926855_2927767_+\|D-amino-acid-aminotransferase	gnl\|CDD\|238799	cd01558, D-AAT_like, D-Alanine aminotransferase (D-AAT_like): D-amino acid aminotransferase catalyzes transamination between D-amino acids and their respective alpha-keto acids. It plays a major role in the synthesis of bacterial cell wall components like D-alanine and D-glutamate in addition to other D-amino acids. The enzyme like other members of this superfamily requires PLP as a cofactor. Members of this subgroup are found in all three forms of life.	7.4093e-91
NZ_CP036280.1\|WP_145446763.1\|2943162_2944656_-\|glycosyl-hydrolase	gnl\|CDD\|350121	cd18609, GH32-like, Glycosyl hydrolase family 32 family protein. The GH32 family contains glycosyl hydrolase family GH32 proteins that cleave sucrose into fructose and glucose via beta-fructofuranosidase activity, producing invert sugar that is a mixture of dextrorotatory D-glucose and levorotatory D-fructose, thus named invertase (EC 3.2.1.26). This family also contains other fructofuranosidases such as inulinase (EC 3.2.1.7), exo-inulinase (EC 3.2.1.80), levanase (EC 3.2.1.65), and transfructosidases such sucrose:sucrose 1-fructosyltransferase (EC 2.4.1.99), fructan:fructan 1-fructosyltransferase (EC 2.4.1.100), sucrose:fructan 6-fructosyltransferase (EC 2.4.1.10), fructan:fructan 6G-fructosyltransferase (EC 2.4.1.243) and levan fructosyltransferases (EC 2.4.1.-). These retaining enzymes (i.e. they retain the configuration at anomeric carbon atom of the substrate) catalyze hydrolysis in two steps involving a covalent glycosyl enzyme intermediate: an aspartate located close to the N-terminus acts as the catalytic nucleophile and a glutamate acts as the general acid/base; a conserved aspartate residue in the Arg-Asp-Pro (RDP) motif stabilizes the transition state. These enzymes are predicted to display a 5-fold beta-propeller fold as found for GH43 and CH68. The breakdown of sucrose is widely used as a carbon or energy source by bacteria, fungi, and plants. Invertase is used commercially in the confectionery industry, since fructose has a sweeter taste than sucrose and a lower tendency to crystallize. A common structural feature of all these enzymes is a 5-bladed beta-propeller domain, similar to GH43, that contains the catalytic acid and catalytic base. A long V-shaped groove, partially enclosed at one end, forms a single extended substrate-binding surface across the face of the propeller.	5.61958e-99
NZ_CP036280.1\|WP_145446762.1\|2940383_2942810_-\|hypothetical-protein	gnl\|CDD\|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	2.20102e-20
NZ_CP036280.1\|WP_145446750.1\|2923972_2925679_+\|4-alpha-glucanotransferase	gnl\|CDD\|237738	PRK14508, PRK14508, 4-alpha-glucanotransferase; Provisional.	0
NZ_CP036280.1\|WP_145446749.1\|2923209_2924094_+\|acyl-CoA-desaturase	gnl\|CDD\|224316	COG1398, OLE1, Fatty-acid desaturase [Lipid metabolism].	4.93984e-68
NZ_CP036280.1\|WP_145446761.1\|2939405_2940413_+\|UDP-2,3-diacylglucosamine-diphosphatase-LpxI	gnl\|CDD\|377632	pfam06230, DUF1009, Protein of unknown function (DUF1009). Family of uncharacterized bacterial proteins.	8.57327e-54
NZ_CP036280.1\|WP_145446748.1\|2922031_2922985_-\|hypothetical-protein	gnl\|CDD\|223200	COG0122, AlkA, 3-methyladenine DNA glycosylase/8-oxoguanine DNA glycosylase [DNA replication, recombination, and repair].	5.01849e-13
NZ_CP036280.1\|WP_145446764.1\|2944749_2945475_+\|HAD-hydrolase-family-protein	gnl\|CDD\|368291	pfam05116, S6PP, Sucrose-6F-phosphate phosphohydrolase. This family consists of Sucrose-6F-phosphate phosphohydrolase proteins found in plants and cyanobacteria. Sucrose-6(F)-phosphate phosphohydrolase catalyzes the final step in the pathway of sucrose biosynthesis.	2.05481e-42
NZ_CP036280.1\|WP_145446751.1\|2925703_2926744_-\|DUF1611-domain-containing-protein	gnl\|CDD\|225902	COG3367, COG3367, Uncharacterized conserved protein [Function unknown].	1.13138e-74
NZ_CP036280.1\|WP_145446747.1\|2921118_2922054_+\|DUF3891-family-protein	gnl\|CDD\|379025	pfam13030, DUF3891, Protein of unknown function (DUF3891). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and archaea. Proteins in this family are approximately 250 amino acids in length.	2.56425e-34
NZ_CP036280.1\|WP_145447308.1\|2945534_2946800_+\|glycosyltransferase	gnl\|CDD\|340830	cd03800, GT4_sucrose_synthase, sucrose-phosphate synthase and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. The sucrose-phosphate synthases in this family may be unique to plants and photosynthetic bacteria. This enzyme catalyzes the synthesis of sucrose 6-phosphate from fructose 6-phosphate and uridine 5'-diphosphate-glucose, a key regulatory step of sucrose metabolism. The activity of this enzyme is regulated by phosphorylation and moderated by the concentration of various metabolites and light.	1.68619e-127
NZ_CP036280.1\|WP_145446759.1\|2936551_2937730_+\|hypothetical-protein	gnl\|CDD\|271213	cd14254, Dockerin_II, Type II dockerin repeat domain. Bacterial cohesin domains bind to a complementary protein domain named dockerin, and this interaction is required for the formation of the cellulosome, a cellulose-degrading complex. The cellulosome consists of scaffoldin, a noncatalytic scaffolding polypeptide, that comprises repeating cohesion modules and a single carbohydrate-binding module (CBM). Specific calcium-dependent interactions between cohesins and dockerins appear to be essential for cellulosome assembly. This subfamily represents type II dockerins, which are responsible for mediating attachment of the cellulosome complex to the bacterial cell wall.	1.99762e-06

>NZ_CP036280.1|WP_145446755.1|2931419_2932541_+|hypothetical-protein
MHRTLAAGVTLAALLAPCANADTRFWHIQNTGYYHDGNDGTALALRNGSVWPTIFTDDGRALAQFATGWTDLVPFNVSLFPRTYDMPLRATSSADHRVTVTTDDQSSGSGYLSNNGVTLSRTGFTPLPDHTLAADYGPDGNLYLLLKNPDTSDRYVPGLPDPEYNDYHDIAVSPFGEVGLIDDRYGFAEYSPLRGDWQYVDFYDLPDPDNRFNNFTAISLEYDALGRPHVLGELDNQAAALDYHPATGWTLTDFTQDLTLNGTFDKAYDLAADSLGNVGTALYLDGFESTANALYYLHHDGDEWSAHLVENDTNLDIRYDAQFGIAYDHEDLPVISYVTNGTIHLAYDPIIVPEPAALTLLSLTALTLARRTR
>NZ_CP036280.1|WP_145446754.1|2930768_2931161_+|hypothetical-protein
MIDLISPTFSDATNLEVFQPWDWDDIEFIPIQTDPEIKDETISHDLGSISGGSAVFDNRPSPTFETYQPTDLIFDPQYLIESGQILSITEPLSLTIADGETIFIEPTGPLACDPFEELGLSGHLIITTID
>NZ_CP036280.1|WP_145446753.1|2928224_2930618_+|hypothetical-protein
MNLRLPWATDDLPSEPHARLETLESRLLLAADGFDEQALRDAILDDNPHAVIAIDHDTTTITIASEQDLNLDQEFSDLYPETYDLVITTEGKLNLSYVDAPNSSGSLEGRTLVDPNNVVTASTSGSASSGAVTLTSTASTARPQRQYNTSQYFPDISLDNVETNWIQDEAVSIRLPLTINSTSSHPIKPGSTCNLTVALVPVDDSSNAQVIHTENDLRLNGLRAGGQKRFNINLTLPEYVDPGEYHIRLSARPEFYATARVHTTSGTITVEDGQRELAAHILHTRLPQTVVAQQRLRGSVTATIRNEGNLNTDPRTPHTFTLHAVSADGTAPIVLAERTQRLGRLQPDATRKVHFRVNTTLVDTGLYTLAVTIDTNSISAAQTNNAAPAPNNDAASAAAQTLEVEPAYHDLSLEINEARLRLPQQILETQTPRIRIPIQVTLEGNTRFARGATYSVETYINTPEGEVVLAARDNLRADRLRPGRAQRINLLATLPDNLDAGTHDLKVRLAASPQTHETNANDNASDNNADAIPLNIQQRVDDLGIEIHSTRINYRSLPSSQEPQALAHATGRAVVNITHQGNARLSRTDQATVELVAISNDGQSVTSLGETTVNLRNMKPGSTKRVTIRTQVIVVDTPEGYSYGVRLLTRQTDSNPANNVDLQSNGLVISSLATTDDNENSDWAPDHALAGEYYFNLATGSNVYNQDERYEMFFSQNLGGQRGTYTVTTDQAQTTVGSGIYLYDKTDDDQATFTLFDYLGGLGGLVLDYTAPGLFDYELELKGTEWSSWKRKQLPVI
>NZ_CP036280.1|WP_145446752.1|2926855_2927767_+|D-amino-acid-aminotransferase
MVQQPTPAADPVVYYNGEFIPSSHANVSVEERGTLFGEGVYEVTRVYNAHPFALDEHLERLLNSLRGIGLKDPQTLAAARELKPASAQLLEIHNLAEALVYWQITRGPAQPRSFLYQPNTRPSVLAIAYPTQPINTAGPPPTTTATLLPDDRWANCWIKSTMLLPNNLAYNQAREAGFGAALLQRHGLITEASNANAMFVRDGKILTHPDDGKILNGITRQIVLNHARNLNIPVAEQPLPIAELNTVDEAFLTGTTTHVTPVLAIDDQPVADAKPGPVALQLHHTLMNDINTRCRITTHATTP
>NZ_CP036280.1|WP_145446751.1|2925703_2926744_-|DUF1611-domain-containing-protein
MAQRIVLLTEGHTSIYYAKTAYSVLRYRAEEVVALLDTQEVGKTAGGLLGVGGDVPVVGDLGDVPDADTLIIGIGVHGGKLPEVMRGHLLKAVERGMTVISGLHEFLSDDADLAAAAEHSGAHLWDVRKNHEHEVAEGRGFEDGCYRLHTVGQDCSVGKMIVSVEVSRALAGRGLSSKFVATGQTGIMVEGDGTPIDTVVADFINGAAEKLVLRNQHHDVMCIEGQGSILHPSYSSVTLGLLHGCRPDGLILCYEAGRTHVKGLDHIALKSLETYRALYESLASEMHPCRVVGVGMNSRRLDDAAFEAEKRRVGEALGLPVADVVREGAGVLADAVERAIRDRQPR
>NZ_CP036280.1|WP_145446750.1|2923972_2925679_+|4-alpha-glucanotransferase
MHTHDPRPMACAGSKSIPPTGSSPCSKPPGSPGTSNEPPSDSRRTTPPAGTGPPSYLVPTMSDPKPDTPLPTLDQRSTGVLLHITSLDGHYGIGDLGRPARHLVHWLKAAGVSWWQVLPITPPSAENSPYESISAFAGWHALISLEDLVADGLLPKKALADIPKLPEDRADYQAAQDIRTRLLRQAHQSFTPSDDYHDFLKNQADWLDDWALHEAIRNTRNGKPWHTWPDDLRLRHKHHIETARHDLADDIDFHKFVQYVFDKQWNALREICRDAGIGLIGDVPIFVGMDAADVWAHRALFDLDRDGRPKAISGVPPDMFSETGQVWDHPLYNWTNHEKTDYAWWAARMRHTLNQFDAVRIDHFLGFLRCWAIPADTRHAPDGKWRKGPAKSFFDAVEQQLGTMAVIAEDLGDVTQQAIDLRDDLGYPGMMVTQFGFGEDHAHHAPHNHPRNCVAYTGTHDNNTLSGFYHESSSETRKRILLYTGKEADSVAEDLTRITLLSQANIAVIPPQDLLGLDTHHRMNIPGKKVGNWTWRLPPGSLTASHAKKIHRLNLLAGRTQPLPATES
>NZ_CP036280.1|WP_145446749.1|2923209_2924094_+|acyl-CoA-desaturase
MDSFFKHFPSFRWPISATRSSHPSLRGGLDWTVIIGLGWLHVVAIAAPWTFTWSGLAWLLVLWYLTGGLGIVLCYHRLLTHRSFACPRWLEYTLTFLACAAWQGRPSHWVGTHRIHHKHSDDEGDPHTPQHGFTWSHIFWTMFKEPEGMKADDFAKDLQRDAGMRWFDKWFVVPQFIIALFLIALGYALGGTELAISWFVWGVALRTVWVWHVTWFVNSATHTWGYRNFKTGEHSTNLWWVAILSFGEGWHNNHHAHPRSATHGMRWFEIDPTNWLIALLEATGLAWNVKRTTL
>NZ_CP036280.1|WP_145446748.1|2922031_2922985_-|hypothetical-protein
MAAERMRGSRLRLSVPSDFDLAEAVCSYGYFLLSPNHWDAERQVFETTLATEDSSLIAIRVSQGDQGDPLVVACHRKLDRGEGVRVKQRLGRVLRVDEDFTGWYAMHAGARRRGFGRLFRSPTLWEDIVKTITGCNTTWTSTIRMNRLLVERVGRGAFPSPGQVRRYGAARLKEHVKVGYRAQRIVDVARGFLDGSIDAGWYASPERTAGEVYEALRGLNGIGPYAAANICQLLGHYDFLAIDSETYRHYCAVKGIERPSNDKELDPLIEAHYEGYRPYRFLAYWYDLWTAYEARVGPSRGWVRERDAGAFTASKLR
>NZ_CP036280.1|WP_145446747.1|2921118_2922054_+|DUF3891-family-protein
MLKTTVDQNVWLVPQHTHAQVSGYLAAYWGNHQGFARPGHYPGSTHPHHWRDEVVLGIAEHDNGWWEYEATPRFNPHDGLPVGLGESIDASPADDGFDQWRSGGFERWHLGINRLAEHHPYAALLIVGHAYWLYAPAFDHLMNEPHANAFRHAIFGDPDTAEGLAADRDATLAFLHDMAKTRQQLIRTLNHNPHLADATRPQHLNPHIRLTQTLDTLSLLLARNDTDTHLLHDVPRAGWHDRVTLRWQHLGHRRYQIDPYPFEIDPLPVTIPAKTASPDDLDPDTPMTTLHRLPHQTLTFEITSATSTSTP
>NZ_CP036280.1|WP_145446746.1|2920532_2921024_-|MarR-family-transcriptional-regulator
MRDMIDGLLDQWSVERPDLDARPMAVVGRVLRLAHRLEGRVERVLEPFGLALWQFDVLATLRRSGPGYCLSPTALTEATMLSSGAMTHRIDRLVSMGWVERRPDPDDRRGRLVALTPAGRDLVDAALEARFEEARAVTDALPVRRRRELADALRVLLLASGGA
>NZ_CP036280.1|WP_145446757.1|2934577_2935405_+|hypothetical-protein
MRSLTLTALAAAAIATAASADPYNDTYPMMSSEEAATTTFNLRPQVGITDWTWQGTTLIESWLVYGAYDNEPATPPNNGIRNFYTWPGAEPYRSASSSNGRHFADSSPSNIYFEHTHAIWADIYNSESHDWDSSVRIGHDTSWYFDTDDPEHPEPTLEEHTHQAFQVITPTTASQWTLIDDLSFALNNESGQIMFEIRLSDHYHASVFGFNQTGSPNDSQHATPNPGDSLIMTWDTEYTGVSNEYQAAFVQAYYSVPEPSAIMLCLALSGILARQ
>NZ_CP036280.1|WP_145446758.1|2935520_2936126_+|hypothetical-protein
MKSRNRSHINPLLPSLCLATAAMTMALTPQRATATDLILGDIPPFETLMLFGGLDYSYNNGVIGESYFAALFVSGDNTSASFAGNFEVGVHESGLVLVDDGAVLRLASGMAIGADVSGYTSRASASGSGTKFVVAIGETYVGKNAGGKLAIEDHVAMHARNLYIGHASGSHGEMVVKSSATVSAVGTNNNYIYAAPPAREN
>NZ_CP036280.1|WP_145446759.1|2936551_2937730_+|hypothetical-protein
MLGRTEVSGKIDPGAYAIEDDAVVSTTGELSIAGDCIMEAGSALRIDIASSGTDSINVTPKASMSGDLTLSKSNPILDINFPNQYVPAPGQKYEVASYTGDLTGVFSNAPLPGVPIDTTHNNEIALMIEYDTDNKDINLTTHYIGDANMDNAVNLLDLSTLASNFDTTPATWSMGNFNTDNTVDLLDLSALATNFGKGQTSQSQAPESFSSIGSPATLSLDGDLTVSDDGGITTPDLTGYTTYTLTAAALTDSIDALEILIESDDLNQEYLGYTIFSNNNVFLQQAGINPLRDSQLLFAEGLLSVQADESDTLLTAAFAGFTPFTTRDIAQIVIPDDATATYEIQAVIDDELYIVTGTLGTAAPLTLIPIPEPSSLAVLALTGLALVRRRAA
>NZ_CP036280.1|WP_145446760.1|2938734_2939355_+|transcriptional-repressor-LexA
MNLTPKQLHILSRIRDIRLARGYSPTMQELADELGVSKVTVFEHVEALIKKGALRRQPNKARSLELCEEVDLPDETTGLKLPLVGTIAAGSPIEAVEQREHLDLESMFTPPGSAGNTFVLQVRGDSMIDEHIAEGDYVICEKRNAARSGQTVVALLDSGEATLKKLYHESGNKIRLQPANDKYEPIIVEAGRVQIQGVAIGVVRSY
>NZ_CP036280.1|WP_145446761.1|2939405_2940413_+|UDP-2,3-diacylglucosamine-diphosphatase-LpxI
MEDRPIGLLAGGGRLPIIEAEGIRAMGRKVACVGFTGQYDPALPELCDYFETAGIVRINRWLKLMKRWDVEQAVMVGYVRKTRMYQPLRIVQNLPDSRAIRLWYRVLRNDKRSQLMLRVLADELHDNGVDLIDTTAFIKRHIAELGVMTRTQPTAEQQADIDFAAPILARMNDLDIGQALAIKERDVIAVEAIEGTDRMIKRAGILCKAGGWTLIKGTKPTKDLRFDVPTVGVSTINNMKSSKAACLVITAGNVIMIDKEDVLAAADAAGICIVGIEPVEGTELPMETLAKYAESMDEPIEALQGSLVKPVGEEADAEAEEGERFESGGSAPAQG
>NZ_CP036280.1|WP_145446762.1|2940383_2942810_-|hypothetical-protein
MTRITSGGVLASTLILALTTTTHADIYQWTASRGIYQSTTLTPDGAGKTAEPYADLQGLNLYKAYLREADLTQANLSNANLADAYLYNATLTNTDLSDAIITEANFGSTTDFGFTATQLYSTASYKNKNLAGIKLYSNDLTGWNLAGQNLASASFYNATLTNTDLSDAIITEANFGSTTDSGFTAAQLYSTASYKNKNLAGIDLRYNDLTGWNLAGQNLTDADFDDANLTNTDLNNADLTDANLDYANLTNTDLSDAIITEANFGSTTDSGFTAGQLYSTASYKNKNLAGIDLRYNDLTAWNLAGQNLTDAYFGLANLANTDLSDALITGADFYRTTDSGFTAAQLYSTASYKNKNLTGIDLGYNDLTGWNLAGQNLTNTDLNNANLTDAYLYNATLTNTDLSDAIITEANFGSTTDSGFTATQLYSTASYKNKNLTGIKLYSNDLTGWNLAGQNLTDTDLDYANLTNTDLNNANLTDANLDYANLTNTDLSDALITGADFYRTTDSGFTAGQLYSTASYKNKNLAGIDLGYNDLTDWDLSNLNLQSVVFNHANLHNTDFTASDLRRSHYYIDRTSGNRMSQRLAGVRNAIHPDGRVKGLILQSSETLRIWDDNPLDESEPAIPITIEQELTIDPAATLRLVFEDNQWGSIIQFADPDTPVALAGTLLLEFDDGLDLQSLQITTYQLFDWTNADITGAFDTILYNGPGTFDTSSLMATGEVTYFSATLLPADANLDGSVDMNDLSILAANFGLPGVFGFTQGDFNGDNTVDLLDLSILASHFGNTAIPEPAAVTILLTLLPLSRRRSA
>NZ_CP036280.1|WP_145446763.1|2943162_2944656_-|glycosyl-hydrolase
MYSSHGFIRSDIGDVDVLYHDGVFHLFHLVLPNHDIIAHAVSTDGMTWRRVNNAMFVGDPGAWDDDMLWTMHVTRDPADNNAWRMLYTGLQRREGGRVQRIGAARSNDLMTWTRVACETHEPRKLQPGYPLAVPGPWYESRTDEGRQWVSCRDPFLFEHEGQRRLLFSARRKHGPLVRRGCVGQAVEVAPDVFEFGPPLHAPGLYDDVEVPGLYELDGRFFLLGSIREDVKVHYWYANTPDGPFENYADNVLLPKGNYAARCCRDDNGWLVFNFFSMTQADGTRKNFLPPPKRLAVNRRGRLQLKSHEAFTDRVTTTERANDTSRYRTVFDNPRARVEAHEDGVTLACTSGYELFVTQQRHADFRLRCRLQLNGSGKCGLVLRLDENANGYYLSLDLFKGVAQLRAWGNSATALGEEAFNYRQLQAGYFIPTPGEPAELEVIAYGQYLECSLDGHVLLTLVDEHYTQGSVGFYAESASLRVQNVIIQELDEPESELF
>NZ_CP036280.1|WP_145446764.1|2944749_2945475_+|HAD-hydrolase-family-protein
MMSDAGRCGWLLVSDIDDTFLGDAGATLRLIREAGRQGVAIALNSSRPWVSVAETVAGLPEGWRPRATITAMGTQVRIDEKEQVAWAERFGGWSRGPFDALAAERGWVAHEAAMQTAYKASYALPEGADRDAVREQILAAGRALVVISGGGDLDVLPVSAGKGPATVYLAGVLGFGMDRVVVAGDSANDLGMFEVAERAIAVGNARAELTSRADPERTYFARGCCAGGIIEGLMAYGVLSD
>NZ_CP036280.1|WP_145447308.1|2945534_2946800_+|glycosyltransferase
MISVHGYVAGQPQLGKPDTGGQVVFVLELAKRFRRLGYRVDLLTRRFERQPAVDKITEGLRVLRVPFGGNKFIRKEDMHDHIADFVTNALAYFRENKLTYDVVNSHYWDAGWSGQRIAEEMEIAHVHTPHSLGSWKKKGMVEAGQPVDDTYRFDERIAKEFLVYRNCDHVIPTTDQQEAILAEDYGVPRDHMTMIPPGMDEARFMPAQPALRAAIQKKHGFKQHDVYAVGRVATNKGYDLLIKSLPYLREAVPKARVVIAAGANSERDKRKVNQLKAIAEEAGVSKHVKWKGYVPDDELADHYRSAAVFAMCSRYEPFGMTAIEAMACGTPTVVTVHGGLHEVINYGTHALYADPKQPYMYAAALATPMLYPELGNRLSIEGARFARRQFGWTGIARRTLAIFNRLIGRYESSERLEGSVE
>NZ_CP036280.1|WP_145446765.1|2946830_2947202_-|hypothetical-protein
MPAAKSSASKIALVVVLLAVAAGVWLFNAGEREARNEYNTVVEELYNQGQYQQTYERLIALIDNDTAGSIEDEVRQTAARAALKVAEQPDANLDHSRTWLQRAHDLDPALLSAMQRQLINADE

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Crispr_ID: NZ_CP036280_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_8

2979574-2986845

TypeI

I-C

Consensus_repeat	Method
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CRISPRCasFinder
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CRT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	PILER-CR

109 spacers

cas2,cas1,cas4,cas7,cas8c,cas5,cas3,WYL

The CRISPR arrays of NZ_CP036280_8

>merge|NZ_CP036280|8|2979574-2986845|CRISPRCasFinder,CRT,PILER-CR
GTAAGTATCCACGCTCCCGCGAAGGGAGCGACGAGGCGGTAGCGGAGTTTGCTTATGTTTATGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGTGCGTTTGGTGTTCCGGGCGTCGGCGTTCAGGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCCCAGACAGGAGCAACACGATGAGCAGCGATGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCCCAGACAGGAGCAACACGATGAGCAGCGATGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCGGACGGCAGCGCGCTGTTCAACGCGGGCGACGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACAACGGTAGACCGAATCTTTAGCCGCACGCGTCACGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGTCGACGGGTGTAGGCCGCGGCTTTGTGGGCGTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTCGAGGTCAGGCCGAGGGATCACCACGATCTCATGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGTGACGGTGGCCGAGGGGTTCATGCGCAGCACTTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGCTCCGACGTCGAGCGGGAGCTCGAATGTTTCGCGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTGAACGAGCTCGAAGCGGCGGAGGGCATCGGCGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCTCCAGGCAAGCGTTCATGTACTCGCATTGAGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTTAAGGCCGATGAAGCATCGGTCGCCGAGATCAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGCGGCTTGGCGAACAGCACCGCCATCGATCCGCAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTTCGAGATCGCCAAGGAGCTCAAGCAGGAAAAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGATGGTGGGCCGATCCCGCCAACTTCAGCAGCGACGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGATCCACCCCCGCCAGCAGCGGCTCACAGCTCAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGCGATGTCAACGACCTGCGTCGATGGCTTATCGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTGAGACTAGCGAAAACGTTGCTTCGCCTACGGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGGGTTTGCTCGTCCCGGTGGCGTCGGAATGACTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCACACGCTCGCGGTGGCTCGAAGTCGAAGGGATCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGTGCTGGACGGACGCGTTGCCGACAACCCCCGGAGGATCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCAGAGTCAAGGTATGTGATATATTTGGTGATATAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTGTGATGGCCTTAATCCGCTGAGGATCAATCTCATGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTCGATGATGGCCTTCATGACGACGAGGTTTTTGTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCACGAGCATCTTCCGATCCACCCGGACTTCGAGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGTGCTCGGCTGGCGACACCTGCCCGAGGGTCCGGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGATGACGAGGTTGCAATTGTCTGGGGGGTTGATGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTTCTGGGAACAGTTTCAGGCTACCGAGATTTATGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTCAACGCGGCGCGGAGGATTCTCGAGCGCGTGGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGCGGCTGGGTGCCCCTGCTCTCGGGCGTGGTGCTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACATCACTATCAATAATCAGGTCAAGTTGACTGAGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCGCTCACGTCACGACATCTCAACACTCATCCCGCTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCGCGCTCGTGATACTCGATGCGGCGACCATCCATGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCGGGCAAGAAACCGCACTACGTGCCAGCAGAGGCGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCTTATGGTGGTTGACCAAGTGGGCGGACTGAAAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCATAGCAGAGGGCCGGTGTGGTGATGAGGTTCAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCCCCCCCTCAATAACCAATCCCCGGATCGCGAATGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTGGGCTTGTTCGCGGCGACCTCCAGCAGGGCGGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTCGATGGCAAGGCGTGTGTTAGGTGTAGGTTTGGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGTTTAAGCGTCATGAGGTGGCGATCCCCAGGACGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACATTCGTCTGGATCATCGGTGTATCTCGCTTGGTTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCTGACGGGGTCCTGGCCTGGGGAGAGCGGGAAGAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCATCACAATCGCTATGAGTGCGGGCGAGGACGATGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCAAGTGACGCTGTGGACCGGTGACGCCGGCGACGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGTTATGCGGGTCTCCCTGCCCCCGGGTGTCTGCTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCAGAGCGGGGCGGTGGCCGAAGTGCAGGACAAGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCGGCGTTGTCGGCGACCCTTTGCGCCGCCACCAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTCGCTCGCCTCCGGCATCTGCCTGGTTATCGAGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACAACATCATCACCATCATTACCATCACCCATATATAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGACCTGGCCGAGCAAGTCGCCCACGCAGGCACCGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCCCGAAGGCGAGCCGTGGTACACGGTGCCGGATGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCGGCACCGTTTTCTATCGCTGGGGTGTTTGCTAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACAGAGCTCGAGGCGATCGACATGGAACAGATGCTCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCGCTCAAGGGCGCGACGACAGTCGCAGCCGAAGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACATGGGACTGGTGGGCCTTTGAGACCTTGGATGAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTGTCCGGTGTGCTGGAGTTTCCGGTGATGTCCAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGAGGCGTATCAGCAGATCCGGTTGTCGATCGAGCGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCGGGCATCGACGCGGATATGCGCAAGAGCCTGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACAACAGGTCCGGGATGAATACCTACTGGGGGATTAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCTAACTGTATTTCGATAGCTCTTAATCTACTGTCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGTGTGGTTGGGGTTTACAAGCAGGATCGGGGGGAGTCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGCAAGCTCTGCACACCTTGCATACATGGCTTTTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTACGCGTTTCGGCAGGGCGTGGACGATGCAAAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGGCGTCACCAAACCGGCAGGAACCGTCTCGATCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGCTTTGGCCCCCTAGGCAATTCCGCCACTTATCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGGGCACCCAGCCGCCGTTCGTGCCGAGCAGCGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTAAGTTATGGCGATTGGAAGCGGAGAGAAGTTAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACAAACTCATTGTGCCCGACGTACCATTACACCGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGATCTTTCACGGGTATATCCCCGCCGAGCGCATGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGATATGGCGGCGCAGGTGGCGATCGACCGGGGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCAAGCGGCAGATCAACAACGTGGTGCGCGACGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACAGCGTTGGGTACTACTATAGTTTCTGGTTCAGGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTTGCGATCTCGGTAGCCGCACCCGCGACCGCCGGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACATCGAAGCCGTTCAGCCTTACGAACCTGCACCGGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGTGCCGGGTCTTCGCGGATCTGGCCCCGTTCATTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGCTCCCCCCTAGATGACCCCAAACGCTCCAAAAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGACGCCGCCAGTTGTCCTTCAATCACGCGATCGGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTTTTAGTGGAGCCGAAGCCGATGCTATCAACGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGTCGTCGGCGCTCGGGGCGAACAACTACCGGTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTATCATTCATACTAAGACGAGCGGCGGTTCTACCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACACACGAGGCCGTCGGCGGTGAGCCGTGGGCGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGATCTGGGGTGGACGGTGGTGTGCCTCTCTGCGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACATGGATGTTTCTGATGTTAGGTGTGACAAGCCTAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCCTACAAGATCCGCACCGAGATCATCCCGCGTGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTTGCCCACGTCCATCGGCAGTTCCGCGTAGGCCGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGACTCTGGCGGTCTTGATCAGATCGTCACAACGTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGATCCAGGCATCATCTGTGCGACAACCTGGGCGTAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTAGTGGGTTGGCTGTTAATGCTAATTTCTGGGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCGATTTTCGGGGTATACTGGTACCGATCCGGCTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGTAGTGAGATAGTAGACACTGAGGAAGTCGAAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCGATGGCGAGTTGGAATTGCAGCGAGAGTATTTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCCCAGGCTCCGGGTAAAAAAAAGCAGTTCACCCATGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCAGGCCGTTCCCACGCGAGCGGCTTGAGTTGGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGATCAAGCCCATAGGACTCAAGCGGGTCAAAGCGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGACGCGAGGCCACGGACCTGATCGAGGACATCAGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGGACCGGACGGGTGGCCGCCCGGCCCCACTGGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACAGCCGGTGCCGTGTCGCGGCCAGATGGGGCTGTGGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCCAGCTGCCGGTGGTGGTGGGTGAGCCGATGGAGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTACCGACCTGACGGCCGACCGTTCCCGACCTGGCTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGCGTCTGCGCCCGCCGGCTGTGGCATCGTTTTGCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCACCGGGACCGTGCGAACTTCCGCGATACGGTCCACGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGAAAGCCTTTGCGCTTTTGGACCGACACGCCAGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTGCTGCTCACCCCCGAAGACGTCGGATCGATCATCGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCGAGCAGAGCCCGACCTACTGCGAGGCGATCGTTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACGGTGGTGTTGTGAGCGCCGCGGCGGGGGCAGTCGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTCTCGCCAACGATGAGCTTCGGCACGCGGGCGGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACCTTTGCCCCGCCCGGCTTCAAGGTCAACGCGGTGTTTCAATCCACGCTCCCGCGAAGGGAGCGACTGCCGGATCACCGGAACCGCCGCCGCCGCACCGTCGTTTCAATCCACGCTCCCGCGAAGGGAGCGAC

>NZ_CP036280|8|8|2979574-2986845|CRISPRCasFinder
GTAAGTATCCACGCTCCCGCGAAGGGAGCGAC	GAGGCGGTAGCGGAGTTTGCTTATGTTTATGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCGTTTGGTGTTCCGGGCGTCGGCGTTCAGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGACAGGAGCAACACGATGAGCAGCGATGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGACAGGAGCAACACGATGAGCAGCGATGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGACGGCAGCGCGCTGTTCAACGCGGGCGACGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACGGTAGACCGAATCTTTAGCCGCACGCGTCAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTCGACGGGTGTAGGCCGCGGCTTTGTGGGCGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TCGAGGTCAGGCCGAGGGATCACCACGATCTCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGACGGTGGCCGAGGGGTTCATGCGCAGCACTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTCCGACGTCGAGCGGGAGCTCGAATGTTTCGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGAACGAGCTCGAAGCGGCGGAGGGCATCGGCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCTCCAGGCAAGCGTTCATGTACTCGCATTGAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTAAGGCCGATGAAGCATCGGTCGCCGAGATCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGGCTTGGCGAACAGCACCGCCATCGATCCGCA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTCGAGATCGCCAAGGAGCTCAAGCAGGAAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATGGTGGGCCGATCCCGCCAACTTCAGCAGCGACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCCACCCCCGCCAGCAGCGGCTCACAGCTCA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGATGTCAACGACCTGCGTCGATGGCTTATCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTGAGACTAGCGAAAACGTTGCTTCGCCTACGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGGTTTGCTCGTCCCGGTGGCGTCGGAATGACT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CACACGCTCGCGGTGGCTCGAAGTCGAAGGGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCTGGACGGACGCGTTGCCGACAACCCCCGGAGGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CAGAGTCAAGGTATGTGATATATTTGGTGATATA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGTGATGGCCTTAATCCGCTGAGGATCAATCTCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TCGATGATGGCCTTCATGACGACGAGGTTTTTGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCACGAGCATCTTCCGATCCACCCGGACTTCGAG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGCTCGGCTGGCGACACCTGCCCGAGGGTCCGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATGACGAGGTTGCAATTGTCTGGGGGGTTGATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTCTGGGAACAGTTTCAGGCTACCGAGATTTAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCAACGCGGCGCGGAGGATTCTCGAGCGCGTGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGGCTGGGTGCCCCTGCTCTCGGGCGTGGTGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATCACTATCAATAATCAGGTCAAGTTGACTGAGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCTCACGTCACGACATCTCAACACTCATCCCGCT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCGCTCGTGATACTCGATGCGGCGACCATCCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGGCAAGAAACCGCACTACGTGCCAGCAGAGGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCTTATGGTGGTTGACCAAGTGGGCGGACTGAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CATAGCAGAGGGCCGGTGTGGTGATGAGGTTCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCCCCCTCAATAACCAATCCCCGGATCGCGAAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGGGCTTGTTCGCGGCGACCTCCAGCAGGGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCGATGGCAAGGCGTGTGTTAGGTGTAGGTTTGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTTTAAGCGTCATGAGGTGGCGATCCCCAGGACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATTCGTCTGGATCATCGGTGTATCTCGCTTGGTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCTGACGGGGTCCTGGCCTGGGGAGAGCGGGAAGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CATCACAATCGCTATGAGTGCGGGCGAGGACGAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAAGTGACGCTGTGGACCGGTGACGCCGGCGAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTTATGCGGGTCTCCCTGCCCCCGGGTGTCTGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CAGAGCGGGGCGGTGGCCGAAGTGCAGGACAAGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGCGTTGTCGGCGACCCTTTGCGCCGCCACCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCGCTCGCCTCCGGCATCTGCCTGGTTATCGAG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACATCATCACCATCATTACCATCACCCATATATA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACCTGGCCGAGCAAGTCGCCCACGCAGGCACCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCCCGAAGGCGAGCCGTGGTACACGGTGCCGGATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGGCACCGTTTTCTATCGCTGGGGTGTTTGCTAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGAGCTCGAGGCGATCGACATGGAACAGATGCTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCTCAAGGGCGCGACGACAGTCGCAGCCGAAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATGGGACTGGTGGGCCTTTGAGACCTTGGATGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGTCCGGTGTGCTGGAGTTTCCGGTGATGTCCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GAGGCGTATCAGCAGATCCGGTTGTCGATCGAGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGGGCATCGACGCGGATATGCGCAAGAGCCTGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACAGGTCCGGGATGAATACCTACTGGGGGATTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCTAACTGTATTTCGATAGCTCTTAATCTACTGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGTGGTTGGGGTTTACAAGCAGGATCGGGGGGAGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCAAGCTCTGCACACCTTGCATACATGGCTTTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTACGCGTTTCGGCAGGGCGTGGACGATGCAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGCGTCACCAAACCGGCAGGAACCGTCTCGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTTTGGCCCCCTAGGCAATTCCGCCACTTATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGGCACCCAGCCGCCGTTCGTGCCGAGCAGCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TAAGTTATGGCGATTGGAAGCGGAGAGAAGTTAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AAACTCATTGTGCCCGACGTACCATTACACCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCTTTCACGGGTATATCCCCGCCGAGCGCATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATATGGCGGCGCAGGTGGCGATCGACCGGGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAAGCGGCAGATCAACAACGTGGTGCGCGACGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGCGTTGGGTACTACTATAGTTTCTGGTTCAGGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTGCGATCTCGGTAGCCGCACCCGCGACCGCCGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATCGAAGCCGTTCAGCCTTACGAACCTGCACCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCCGGGTCTTCGCGGATCTGGCCCCGTTCATT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTCCCCCCTAGATGACCCCAAACGCTCCAAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACGCCGCCAGTTGTCCTTCAATCACGCGATCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTTTAGTGGAGCCGAAGCCGATGCTATCAACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTCGTCGGCGCTCGGGGCGAACAACTACCGGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TATCATTCATACTAAGACGAGCGGCGGTTCTACC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ACACGAGGCCGTCGGCGGTGAGCCGTGGGCGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCTGGGGTGGACGGTGGTGTGCCTCTCTGCGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATGGATGTTTCTGATGTTAGGTGTGACAAGCCTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCCTACAAGATCCGCACCGAGATCATCCCGCGTGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTGCCCACGTCCATCGGCAGTTCCGCGTAGGCCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACTCTGGCGGTCTTGATCAGATCGTCACAACGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGATCCAGGCATCATCTGTGCGACAACCTGGGCGTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TAGTGGGTTGGCTGTTAATGCTAATTTCTGGGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCGATTTTCGGGGTATACTGGTACCGATCCGGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTAGTGAGATAGTAGACACTGAGGAAGTCGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGATGGCGAGTTGGAATTGCAGCGAGAGTATTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGGCTCCGGGTAAAAAAAAGCAGTTCACCCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAGGCCGTTCCCACGCGAGCGGCTTGAGTTGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCAAGCCCATAGGACTCAAGCGGGTCAAAGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACGCGAGGCCACGGACCTGATCGAGGACATCAGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGACCGGACGGGTGGCCGCCCGGCCCCACTGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGCCGGTGCCGTGTCGCGGCCAGATGGGGCTGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAGCTGCCGGTGGTGGTGGGTGAGCCGATGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TACCGACCTGACGGCCGACCGTTCCCGACCTGGCT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGTCTGCGCCCGCCGGCTGTGGCATCGTTTTGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CACCGGGACCGTGCGAACTTCCGCGATACGGTCCAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GAAAGCCTTTGCGCTTTTGGACCGACACGCCAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGCTGCTCACCCCCGAAGACGTCGGATCGATCATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGAGCAGAGCCCGACCTACTGCGAGGCGATCGTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGGTGTTGTGAGCGCCGCGGCGGGGGCAGTCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCTCGCCAACGATGAGCTTCGGCACGCGGGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTTGCCCCGCCCGGCTTCAAGGTCAACGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGCCGGATCACCGGAACCGCCGCCGCCGCACCGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC

>NZ_CP036280|8|1|2979574-2986845|CRT
GTAAGTATCCACGCTCCCGCGAAGGGAGCGAC	GAGGCGGTAGCGGAGTTTGCTTATGTTTATGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCGTTTGGTGTTCCGGGCGTCGGCGTTCAGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGACAGGAGCAACACGATGAGCAGCGATGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGACAGGAGCAACACGATGAGCAGCGATGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGACGGCAGCGCGCTGTTCAACGCGGGCGACGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACGGTAGACCGAATCTTTAGCCGCACGCGTCAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTCGACGGGTGTAGGCCGCGGCTTTGTGGGCGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TCGAGGTCAGGCCGAGGGATCACCACGATCTCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGACGGTGGCCGAGGGGTTCATGCGCAGCACTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTCCGACGTCGAGCGGGAGCTCGAATGTTTCGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGAACGAGCTCGAAGCGGCGGAGGGCATCGGCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCTCCAGGCAAGCGTTCATGTACTCGCATTGAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTAAGGCCGATGAAGCATCGGTCGCCGAGATCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGGCTTGGCGAACAGCACCGCCATCGATCCGCA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTCGAGATCGCCAAGGAGCTCAAGCAGGAAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATGGTGGGCCGATCCCGCCAACTTCAGCAGCGACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCCACCCCCGCCAGCAGCGGCTCACAGCTCA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGATGTCAACGACCTGCGTCGATGGCTTATCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTGAGACTAGCGAAAACGTTGCTTCGCCTACGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGGTTTGCTCGTCCCGGTGGCGTCGGAATGACT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CACACGCTCGCGGTGGCTCGAAGTCGAAGGGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCTGGACGGACGCGTTGCCGACAACCCCCGGAGGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CAGAGTCAAGGTATGTGATATATTTGGTGATATA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGTGATGGCCTTAATCCGCTGAGGATCAATCTCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TCGATGATGGCCTTCATGACGACGAGGTTTTTGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCACGAGCATCTTCCGATCCACCCGGACTTCGAG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGCTCGGCTGGCGACACCTGCCCGAGGGTCCGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATGACGAGGTTGCAATTGTCTGGGGGGTTGATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTCTGGGAACAGTTTCAGGCTACCGAGATTTAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCAACGCGGCGCGGAGGATTCTCGAGCGCGTGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGGCTGGGTGCCCCTGCTCTCGGGCGTGGTGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATCACTATCAATAATCAGGTCAAGTTGACTGAGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCTCACGTCACGACATCTCAACACTCATCCCGCT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCGCTCGTGATACTCGATGCGGCGACCATCCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGGCAAGAAACCGCACTACGTGCCAGCAGAGGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCTTATGGTGGTTGACCAAGTGGGCGGACTGAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CATAGCAGAGGGCCGGTGTGGTGATGAGGTTCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCCCCCTCAATAACCAATCCCCGGATCGCGAAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGGGCTTGTTCGCGGCGACCTCCAGCAGGGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCGATGGCAAGGCGTGTGTTAGGTGTAGGTTTGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTTTAAGCGTCATGAGGTGGCGATCCCCAGGACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATTCGTCTGGATCATCGGTGTATCTCGCTTGGTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCTGACGGGGTCCTGGCCTGGGGAGAGCGGGAAGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CATCACAATCGCTATGAGTGCGGGCGAGGACGAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAAGTGACGCTGTGGACCGGTGACGCCGGCGAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTTATGCGGGTCTCCCTGCCCCCGGGTGTCTGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CAGAGCGGGGCGGTGGCCGAAGTGCAGGACAAGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGCGTTGTCGGCGACCCTTTGCGCCGCCACCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCGCTCGCCTCCGGCATCTGCCTGGTTATCGAG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACATCATCACCATCATTACCATCACCCATATATA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACCTGGCCGAGCAAGTCGCCCACGCAGGCACCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCCCGAAGGCGAGCCGTGGTACACGGTGCCGGATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGGCACCGTTTTCTATCGCTGGGGTGTTTGCTAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGAGCTCGAGGCGATCGACATGGAACAGATGCTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCTCAAGGGCGCGACGACAGTCGCAGCCGAAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATGGGACTGGTGGGCCTTTGAGACCTTGGATGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGTCCGGTGTGCTGGAGTTTCCGGTGATGTCCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GAGGCGTATCAGCAGATCCGGTTGTCGATCGAGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGGGCATCGACGCGGATATGCGCAAGAGCCTGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACAGGTCCGGGATGAATACCTACTGGGGGATTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCTAACTGTATTTCGATAGCTCTTAATCTACTGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGTGGTTGGGGTTTACAAGCAGGATCGGGGGGAGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCAAGCTCTGCACACCTTGCATACATGGCTTTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTACGCGTTTCGGCAGGGCGTGGACGATGCAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGCGTCACCAAACCGGCAGGAACCGTCTCGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTTTGGCCCCCTAGGCAATTCCGCCACTTATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGGCACCCAGCCGCCGTTCGTGCCGAGCAGCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TAAGTTATGGCGATTGGAAGCGGAGAGAAGTTAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AAACTCATTGTGCCCGACGTACCATTACACCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCTTTCACGGGTATATCCCCGCCGAGCGCATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATATGGCGGCGCAGGTGGCGATCGACCGGGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAAGCGGCAGATCAACAACGTGGTGCGCGACGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGCGTTGGGTACTACTATAGTTTCTGGTTCAGGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTGCGATCTCGGTAGCCGCACCCGCGACCGCCGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATCGAAGCCGTTCAGCCTTACGAACCTGCACCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCCGGGTCTTCGCGGATCTGGCCCCGTTCATT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTCCCCCCTAGATGACCCCAAACGCTCCAAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACGCCGCCAGTTGTCCTTCAATCACGCGATCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTTTAGTGGAGCCGAAGCCGATGCTATCAACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTCGTCGGCGCTCGGGGCGAACAACTACCGGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TATCATTCATACTAAGACGAGCGGCGGTTCTACC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ACACGAGGCCGTCGGCGGTGAGCCGTGGGCGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCTGGGGTGGACGGTGGTGTGCCTCTCTGCGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATGGATGTTTCTGATGTTAGGTGTGACAAGCCTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCCTACAAGATCCGCACCGAGATCATCCCGCGTGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTGCCCACGTCCATCGGCAGTTCCGCGTAGGCCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACTCTGGCGGTCTTGATCAGATCGTCACAACGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGATCCAGGCATCATCTGTGCGACAACCTGGGCGTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TAGTGGGTTGGCTGTTAATGCTAATTTCTGGGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCGATTTTCGGGGTATACTGGTACCGATCCGGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTAGTGAGATAGTAGACACTGAGGAAGTCGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGATGGCGAGTTGGAATTGCAGCGAGAGTATTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGGCTCCGGGTAAAAAAAAGCAGTTCACCCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAGGCCGTTCCCACGCGAGCGGCTTGAGTTGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCAAGCCCATAGGACTCAAGCGGGTCAAAGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACGCGAGGCCACGGACCTGATCGAGGACATCAGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGACCGGACGGGTGGCCGCCCGGCCCCACTGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGCCGGTGCCGTGTCGCGGCCAGATGGGGCTGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAGCTGCCGGTGGTGGTGGGTGAGCCGATGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TACCGACCTGACGGCCGACCGTTCCCGACCTGGCT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGTCTGCGCCCGCCGGCTGTGGCATCGTTTTGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CACCGGGACCGTGCGAACTTCCGCGATACGGTCCAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GAAAGCCTTTGCGCTTTTGGACCGACACGCCAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGCTGCTCACCCCCGAAGACGTCGGATCGATCATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGAGCAGAGCCCGACCTACTGCGAGGCGATCGTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGGTGTTGTGAGCGCCGCGGCGGGGGCAGTCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCTCGCCAACGATGAGCTTCGGCACGCGGGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTTGCCCCGCCCGGCTTCAAGGTCAACGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGCCGGATCACCGGAACCGCCGCCGCCGCACCGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC

>NZ_CP036280|8|1|2979639-2986845|PILER-CR
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCGTTTGGTGTTCCGGGCGTCGGCGTTCAGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGACAGGAGCAACACGATGAGCAGCGATGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGACAGGAGCAACACGATGAGCAGCGATGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGACGGCAGCGCGCTGTTCAACGCGGGCGACGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACGGTAGACCGAATCTTTAGCCGCACGCGTCAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTCGACGGGTGTAGGCCGCGGCTTTGTGGGCGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TCGAGGTCAGGCCGAGGGATCACCACGATCTCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGACGGTGGCCGAGGGGTTCATGCGCAGCACTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTCCGACGTCGAGCGGGAGCTCGAATGTTTCGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGAACGAGCTCGAAGCGGCGGAGGGCATCGGCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCTCCAGGCAAGCGTTCATGTACTCGCATTGAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTAAGGCCGATGAAGCATCGGTCGCCGAGATCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGGCTTGGCGAACAGCACCGCCATCGATCCGCA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTCGAGATCGCCAAGGAGCTCAAGCAGGAAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATGGTGGGCCGATCCCGCCAACTTCAGCAGCGACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCCACCCCCGCCAGCAGCGGCTCACAGCTCA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGATGTCAACGACCTGCGTCGATGGCTTATCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTGAGACTAGCGAAAACGTTGCTTCGCCTACGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGGTTTGCTCGTCCCGGTGGCGTCGGAATGACT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CACACGCTCGCGGTGGCTCGAAGTCGAAGGGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCTGGACGGACGCGTTGCCGACAACCCCCGGAGGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CAGAGTCAAGGTATGTGATATATTTGGTGATATA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGTGATGGCCTTAATCCGCTGAGGATCAATCTCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TCGATGATGGCCTTCATGACGACGAGGTTTTTGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCACGAGCATCTTCCGATCCACCCGGACTTCGAG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGCTCGGCTGGCGACACCTGCCCGAGGGTCCGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATGACGAGGTTGCAATTGTCTGGGGGGTTGATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTCTGGGAACAGTTTCAGGCTACCGAGATTTAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCAACGCGGCGCGGAGGATTCTCGAGCGCGTGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCGGCTGGGTGCCCCTGCTCTCGGGCGTGGTGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATCACTATCAATAATCAGGTCAAGTTGACTGAGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCTCACGTCACGACATCTCAACACTCATCCCGCT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCGCTCGTGATACTCGATGCGGCGACCATCCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGGCAAGAAACCGCACTACGTGCCAGCAGAGGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCTTATGGTGGTTGACCAAGTGGGCGGACTGAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CATAGCAGAGGGCCGGTGTGGTGATGAGGTTCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCCCCCTCAATAACCAATCCCCGGATCGCGAAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGGGCTTGTTCGCGGCGACCTCCAGCAGGGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCGATGGCAAGGCGTGTGTTAGGTGTAGGTTTGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTTTAAGCGTCATGAGGTGGCGATCCCCAGGACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATTCGTCTGGATCATCGGTGTATCTCGCTTGGTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCTGACGGGGTCCTGGCCTGGGGAGAGCGGGAAGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CATCACAATCGCTATGAGTGCGGGCGAGGACGAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAAGTGACGCTGTGGACCGGTGACGCCGGCGAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTTATGCGGGTCTCCCTGCCCCCGGGTGTCTGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CAGAGCGGGGCGGTGGCCGAAGTGCAGGACAAGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGGCGTTGTCGGCGACCCTTTGCGCCGCCACCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCGCTCGCCTCCGGCATCTGCCTGGTTATCGAG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACATCATCACCATCATTACCATCACCCATATATA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACCTGGCCGAGCAAGTCGCCCACGCAGGCACCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCCCGAAGGCGAGCCGTGGTACACGGTGCCGGATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGGCACCGTTTTCTATCGCTGGGGTGTTTGCTAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGAGCTCGAGGCGATCGACATGGAACAGATGCTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGCTCAAGGGCGCGACGACAGTCGCAGCCGAAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATGGGACTGGTGGGCCTTTGAGACCTTGGATGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGTCCGGTGTGCTGGAGTTTCCGGTGATGTCCAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GAGGCGTATCAGCAGATCCGGTTGTCGATCGAGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGGGCATCGACGCGGATATGCGCAAGAGCCTGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AACAGGTCCGGGATGAATACCTACTGGGGGATTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCTAACTGTATTTCGATAGCTCTTAATCTACTGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTGTGGTTGGGGTTTACAAGCAGGATCGGGGGGAGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCAAGCTCTGCACACCTTGCATACATGGCTTTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTACGCGTTTCGGCAGGGCGTGGACGATGCAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGCGTCACCAAACCGGCAGGAACCGTCTCGATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTTTGGCCCCCTAGGCAATTCCGCCACTTATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGGCACCCAGCCGCCGTTCGTGCCGAGCAGCGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TAAGTTATGGCGATTGGAAGCGGAGAGAAGTTAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AAACTCATTGTGCCCGACGTACCATTACACCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCTTTCACGGGTATATCCCCGCCGAGCGCATG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATATGGCGGCGCAGGTGGCGATCGACCGGGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAAGCGGCAGATCAACAACGTGGTGCGCGACGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGCGTTGGGTACTACTATAGTTTCTGGTTCAGGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTGCGATCTCGGTAGCCGCACCCGCGACCGCCGG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATCGAAGCCGTTCAGCCTTACGAACCTGCACCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGCCGGGTCTTCGCGGATCTGGCCCCGTTCATT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGCTCCCCCCTAGATGACCCCAAACGCTCCAAAAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACGCCGCCAGTTGTCCTTCAATCACGCGATCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTTTAGTGGAGCCGAAGCCGATGCTATCAACG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GTCGTCGGCGCTCGGGGCGAACAACTACCGGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TATCATTCATACTAAGACGAGCGGCGGTTCTACC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ACACGAGGCCGTCGGCGGTGAGCCGTGGGCGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCTGGGGTGGACGGTGGTGTGCCTCTCTGCGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	ATGGATGTTTCTGATGTTAGGTGTGACAAGCCTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCCTACAAGATCCGCACCGAGATCATCCCGCGTGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TTGCCCACGTCCATCGGCAGTTCCGCGTAGGCCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACTCTGGCGGTCTTGATCAGATCGTCACAACGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGATCCAGGCATCATCTGTGCGACAACCTGGGCGTA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TAGTGGGTTGGCTGTTAATGCTAATTTCTGGGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCGATTTTCGGGGTATACTGGTACCGATCCGGCTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTAGTGAGATAGTAGACACTGAGGAAGTCGAA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGATGGCGAGTTGGAATTGCAGCGAGAGTATTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCCCAGGCTCCGGGTAAAAAAAAGCAGTTCACCCAT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAGGCCGTTCCCACGCGAGCGGCTTGAGTTGGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GATCAAGCCCATAGGACTCAAGCGGGTCAAAGCG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GACGCGAGGCCACGGACCTGATCGAGGACATCAGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGGACCGGACGGGTGGCCGCCCGGCCCCACTGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	AGCCGGTGCCGTGTCGCGGCCAGATGGGGCTGTG
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CCAGCTGCCGGTGGTGGTGGGTGAGCCGATGGA
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TACCGACCTGACGGCCGACCGTTCCCGACCTGGCT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GCGTCTGCGCCCGCCGGCTGTGGCATCGTTTTGC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CACCGGGACCGTGCGAACTTCCGCGATACGGTCCAC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GAAAGCCTTTGCGCTTTTGGACCGACACGCCAGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGCTGCTCACCCCCGAAGACGTCGGATCGATCATC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CGAGCAGAGCCCGACCTACTGCGAGGCGATCGTT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	GGTGGTGTTGTGAGCGCCGCGGCGGGGGCAGTCGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTCTCGCCAACGATGAGCTTCGGCACGCGGGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	CTTTGCCCCGCCCGGCTTCAAGGTCAACGCGGT
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC	TGCCGGATCACCGGAACCGCCGCCGCCGCACCGTC
GTTTCAATCCACGCTCCCGCGAAGGGAGCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145446796.1\|2992503_2994789_-\|CRISPR-associated-endonuclease-Cas3''	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|350688
NZ_CP036280.1\|WP_145446788.1\|2975514_2976171_-\|plasmid-pRiA4b-ORF-3-family-protein	unknown	unknown	gnl\|CDD\|377943
NZ_CP036280.1\|WP_145446799.1\|2997249_2999130_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|374201
NZ_CP036280.1\|WP_145446784.1\|2969661_2971137_-\|tyrosine-type-recombinase/integrase	unknown	unknown	gnl\|CDD\|271175
NZ_CP036280.1\|WP_145447314.1\|2973685_2973883_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378935
NZ_CP036280.1\|WP_145446789.1\|2976394_2979523_-\|DUF3427-domain-containing-protein	unknown	unknown	gnl\|CDD\|197297
NZ_CP036280.1\|WP_145446787.1\|2975097_2975454_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446790.1\|2987025_2987316_-\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP036280.1\|WP_145446792.1\|2988349_2989027_-\|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl\|CDD\|187768
NZ_CP036280.1\|WP_145446797.1\|2995157_2996132_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379536
NZ_CP036280.1\|WP_145446795.1\|2991781_2992504_-\|type-I-C-CRISPR-associated-protein-Cas5	cas5	cd09752_cas5_CAS-I-C	gnl\|CDD\|187534
NZ_CP036280.1\|WP_145446785.1\|2971349_2973689_-\|DUF3987-domain-containing-protein	unknown	unknown	gnl\|CDD\|379041
NZ_CP036280.1\|WP_145446786.1\|2974166_2975105_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|240439
NZ_CP036280.1\|WP_145446798.1\|2996190_2997177_-\|WYL-domain-containing-protein	WYL	pfam13280_WYL_CAS-I:CAS-III	gnl\|CDD\|379100
NZ_CP036280.1\|WP_145446791.1\|2987318_2988353_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	cas1	cd09721_cas1_CAS-I-C	gnl\|CDD\|188360
NZ_CP036280.1\|WP_145446781.1\|2965126_2965861_-\|DNA-repair-protein-RecO	unknown	unknown	gnl\|CDD\|234622
NZ_CP036280.1\|WP_145446794.1\|2989934_2991785_-\|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	cas8c	pfam09709_cas8c_CAS-I-C	gnl\|CDD\|378245
NZ_CP036280.1\|WP_145446782.1\|2965887_2966826_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446793.1\|2989029_2989938_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	cas7	cd09689_cas7_CAS-I-C	gnl\|CDD\|377458
NZ_CP036280.1\|WP_145446783.1\|2967062_2969093_+\|ammonium-transporter	unknown	unknown	gnl\|CDD\|223083

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145446796.1\|2992503_2994789_-\|CRISPR-associated-endonuclease-Cas3''	gnl\|CDD\|350688	cd17930, DEXHc_cas3, DEXH/Q-box helicase domain of Cas3. CRISPR-associated (Cas) 3 is a nuclease-helicase responsible for degradation of dsDNA. The two enzymatic units of Cas3, a histidine-aspartate (HD) nuclease and a Superfamily 2 (SF2) helicase, may be expressed from separate genes as Cas3' (SF2 helicase) and Cas3'' (HD nuclease) or may be fused as a single HD-SF2 polypeptide. The nucleolytic activity of most Cas3 enzymes is transition metal ion-dependent. Cas3 is a member of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	1.73818e-54
NZ_CP036280.1\|WP_145446788.1\|2975514_2976171_-\|plasmid-pRiA4b-ORF-3-family-protein	gnl\|CDD\|377943	pfam07929, PRiA4_ORF3, Plasmid pRiA4b ORF-3-like protein. Members of this family are similar to the protein product of ORF-3 found on plasmid pRiA4 in the bacterium Agrobacterium rhizogenes. This plasmid is responsible for tumorigenesis at wound sites of plants infected by this bacterium, but the ORF-3 product does not seem to be involved in the pathogenetic process. Other proteins found in this family are annotated as being putative TnpR resolvases, but no further evidence was found to back this. Moreover, another member of this family is described as a probable lexA repressor and in fact carries a LexA DNA binding domain (pfam01726), but no references were found to expand on this.	1.33979e-77
NZ_CP036280.1\|WP_145446799.1\|2997249_2999130_-\|hypothetical-protein	gnl\|CDD\|374201	pfam15892, BNR_4, BNR repeat-containing family member. BNR_4 is a family which carries the unique sequence motif SxDxGxTW which is so characteristic of the repeats of the BNR family, pfam02012. It is unclear whether or not this unit is repeated throughout the sequences of this family, but if it is then the family is likely to be bacterial neuraminidase.	1.52379e-09
NZ_CP036280.1\|WP_145446784.1\|2969661_2971137_-\|tyrosine-type-recombinase/integrase	gnl\|CDD\|271175	cd00397, DNA_BRE_C, DNA breaking-rejoining enzymes, C-terminal catalytic domain. The DNA breaking-rejoining enzyme superfamily includes type IB topoisomerases and tyrosine based site-specific recombinases (integrases) that share the same fold in their catalytic domain containing conserved active site residues. The best-studied members of this diverse superfamily include Human topoisomerase I, the bacteriophage lambda integrase, the bacteriophage P1 Cre recombinase, the yeast Flp recombinase, and the bacterial XerD/C recombinases. Their overall reaction mechanism is essentially identical and involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA. The enzymes differ in that topoisomerases cleave and then rejoin the same 5' and 3' termini, whereas a site-specific recombinase transfers a 5' hydroxyl generated by recombinase cleavage to a new 3' phosphate partner located in a different duplex region. Many DNA breaking-rejoining enzymes also have N-terminal domains, which show little sequence or structure similarity.	1.39707e-14
NZ_CP036280.1\|WP_145447314.1\|2973685_2973883_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	1.06437e-10
NZ_CP036280.1\|WP_145446795.1\|2991781_2992504_-\|type-I-C-CRISPR-associated-protein-Cas5	gnl\|CDD\|187534	cd09752, Cas5_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas5. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas5 is a RAMP superfamily protein; Subunit of the Cascade complex; in subtype I-C this protein might be the endoribonuclease that generates crRNAs; also known as DevS family.	1.75844e-87
NZ_CP036280.1\|WP_145446790.1\|2987025_2987316_-\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	6.56078e-32
NZ_CP036280.1\|WP_145446792.1\|2988349_2989027_-\|CRISPR-associated-protein-Cas4	gnl\|CDD\|187768	cd09637, Cas4_I-A_I-B_I-C_I-D_II-B, CRISPR/Cas system-associated protein Cas4. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas4 is RecB-like nuclease with three-cysteine C-terminal cluster.	2.57253e-36
NZ_CP036280.1\|WP_145446797.1\|2995157_2996132_-\|hypothetical-protein	gnl\|CDD\|379536	pfam14281, PDDEXK_4, PD-(D/E)XK nuclease superfamily. Members of this family belong to the PD-(D/E)XK nuclease superfamily.	5.14165e-06
NZ_CP036280.1\|WP_145446785.1\|2971349_2973689_-\|DUF3987-domain-containing-protein	gnl\|CDD\|379041	pfam13148, DUF3987, Protein of unknown function (DUF3987). A family of uncharacterized proteins found by clustering human gut metagenomic sequences.	3.35018e-83
NZ_CP036280.1\|WP_145446786.1\|2974166_2975105_-\|hypothetical-protein	gnl\|CDD\|240439	PTZ00491, PTZ00491, major vault protein; Provisional.	0.00299158
NZ_CP036280.1\|WP_145446798.1\|2996190_2997177_-\|WYL-domain-containing-protein	gnl\|CDD\|379100	pfam13280, WYL, WYL domain. WYL is a Sm-like SH3 beta-barrel fold containing domain. It is a member of the WYL-like superfamily, named for three conserved amino acids found in a subset of the superfamily. However, these residues are not strongly conserved throughout the family. Rather, the conservation pattern includes four basic residues and a position often occupied by a cysteine, which are predicted to line a ligand-binding groove typical of the Sm-like SH3 beta-barrels. A WYL domain protein (sll7009) is a negative regulator of the I-D CRISPR-Cas system in Synechocystis sp. It is predicted to be a ligand-sensing domain that could bind negatively charged ligands, such as nucleotides or nucleic acid fragments, to regulate CRISPR-Cas and other defense systems such as the abortive infection AbiG system.	7.78869e-39
NZ_CP036280.1\|WP_145446791.1\|2987318_2988353_-\|type-I-C-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|188360	TIGR03640, cas1_DVULG, CRISPR-associated endonuclease Cas1, subtype I-C/DVULG. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes the Cas1 protein particular to the DVULG subtype of CRISPR/Cas system.	2.62802e-175
NZ_CP036280.1\|WP_145446781.1\|2965126_2965861_-\|DNA-repair-protein-RecO	gnl\|CDD\|234622	PRK00085, recO, DNA repair protein RecO; Reviewed.	1.31175e-31
NZ_CP036280.1\|WP_145446794.1\|2989934_2991785_-\|type-I-C-CRISPR-associated-protein-Cas8c/Csd1	gnl\|CDD\|378245	pfam09709, Cas_Csd1, CRISPR-associated protein (Cas_Csd1). CRISPR loci appear to be mobile elements with a wide host range. This entry represents proteins that tend to be found near CRISPR repeats. The species range, so far, is exclusively bacterial and mesophilic, although CRISPR loci are particularly common among the archaea and thermophilic bacteria. Clusters of short DNA repeats with nonhomologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins.	0
NZ_CP036280.1\|WP_145446789.1\|2976394_2979523_-\|DUF3427-domain-containing-protein	gnl\|CDD\|197297	cd09203, PLDc_N_DEXD_b1, N-terminal putative catalytic domain of uncharacterized prokaryotic and archeal HKD family nucleases fused to a DEAD/DEAH box helicase domain. N-terminal putative catalytic domain of uncharacterized prokaryotic and archeal HKD family nucleases fused to a DEAD/DEAH box helicase domain. All members of this subfamily are uncharacterized. Other characterized members of the superfamily that have a related domain architecture ( containing a DEAD/DEAH box helicase domain), include the DNA/RNA helicase superfamily II (SF2) and Res-subunit of type III restriction endonucleases. In addition to the helicase-like region, members of this subfamily also contain one copy of the conserved HKD motif (H-x-K-x(4)-D, where x represents any amino acid residue) in the N-terminal putative catalytic domain. The HKD motif characterizes the phospholipase D (PLD, EC 3.1.4.4) superfamily.	7.58868e-79
NZ_CP036280.1\|WP_145446793.1\|2989029_2989938_-\|type-I-C-CRISPR-associated-protein-Cas7/Csd2	gnl\|CDD\|377458	pfam05107, Cas_Cas7, CRISPR-associated protein Cas7. CRISPR-associated protein Cas7 is one of the components of the type I-B cascade-like antiviral defense complex. In Haloferax volcanii, Cas5, Cas6 and Cas7 form a small complex that aids the stability of CRISPR-derived RNA.	1.19977e-141
NZ_CP036280.1\|WP_145446783.1\|2967062_2969093_+\|ammonium-transporter	gnl\|CDD\|223083	COG0004, AmtB, Ammonia permease [Inorganic ion transport and metabolism].	2.69445e-127

>NZ_CP036280.1|WP_145446789.1|2976394_2979523_-|DUF3427-domain-containing-protein
MPQSEAPRLPPGLYDQLLTGALREQLDRDGGLLPKRTSDIDADEAHAAIAQHLEHLLALSLSTLRGKDAAEKQVRLVDRLIATLREELGDDWGERFRLDNPLRRLLAVHAKDEPGSLKRPDTPLARSALLTGTRVDPSLASQLAAEFAAADRVDILCSFIKWSGLRLLLDSLKSLTATPHPEGLPRLRIISTSYMGATDPKAIEALAALPHTEIKVSYDTERTRLHAKAYLVHRATGFGSAYVGSANLSRAALSEGLEWTSKISQYELAHLWQKVTATFESYWNDAEFEAYAADAPERLRRAIDREKQWGAVSMGEMPAFDLRPYPFQEEILDALAAERQVRDKHRHLMVAATGTGKTMIAGFDYHRWAAGSRPSLLFIAHREEILRQALGTFRGILRDQNFGDLLVGGEHPEQHDHLFCSIQRYNSRGLHQLPPDRFDYVVIDEFHHAAAPSYQRLLEWIQPRVLLGLTATPERADGLDVLKHFGGEATAEVRLPDAIERRLLCPFHYFGVADSVDLQGIRWQRGGYNVEDLDQLYTGNDVRAGLVLEKVYQTLLDPRAARGLGFCVSIAHASFMARFFNQHGVPAMSLSSESSDEERCSARERLVRREINFIFVVDLYNEGVDIPEVDTVLFLRPTESLTLYLQQLGRGLRLNDEKDCLTVLDFIGTQRREFRFASRFRALSTDPTGRLEQEIENGFPHLPSGSFIQLERVAQQRVLENVRQSLNLRRPQMIRDLRELGRHLDRPPRLHEALEYLDTTLDEVLKRGLWSRLLHDAELVAEPNVRDEDQLAKGIRRLAHLDDPAHIRFLLGHLQKDLLDDPLRDLRRSILHGTLWGSGGISMGLDEADQRLQGQHSVVSDLKAVMEYRLRNTQTAGGPLDSNLTGPLALHARYTRDEILIGLGHWTQTHRPDFREGVLHLSEKRIDAFFVTLQKTEDAYSPTTMYEDYAISDRLFHWQSQSTTSVESKTGQRYIYHQAVGYTPLLFVRERKYGPGGLAMPYVFLGSAGYVSHEGSRPVSIVWRLEHAMPQRIGRIAKSSVA
>NZ_CP036280.1|WP_145446788.1|2975514_2976171_-|plasmid-pRiA4b-ORF-3-family-protein
MSTLIHTLRITLQDSKPPIWRRVAVPSDITLGQLHEVIQISMGWTNSHLHQFVLRDKSLKPSRDEIRKVGEADIWDDAFMARMRGERVFSMLTTPFGDPTEMEGEDEDAVTLAEVCPKVKSKLTYEYDFGDGWEHTIEVQKIEEPKPGVEYPVCLAGKLACPPEDCGGIYGYDHTLDVVADADHEEHDDLVEWLGDDFDPEAFDIDEVNDILAEWREG
>NZ_CP036280.1|WP_145446787.1|2975097_2975454_-|hypothetical-protein
MENINAWCASARGEDLWRDTVEHRMWADRLRDEAKGIIIWLELRGQDDAAAQLDEAMGAFRQAVWCFEEACRGVYPADDPGCRDARDAMIDAAGRASGVAEDLDSELPADVWEGFFDA
>NZ_CP036280.1|WP_145446786.1|2974166_2975105_-|hypothetical-protein
MPDLADMVQSVLDAHAAGQAVDLARSEQWLQVRQRYSEFSVNLIVNGHESLARRIDREYQALREAMLHAVESQNGKSVADDYALWEAVTEFQFTVGHLERRHRQLDSMSHVEPAKQLPKPGGKADPPKRSWTQGDLDDAIREYKAKRASSYQRLLSVLDDPKSSPSSKRTARKQAKELFGRNVIARALGVKSAKMVSQSQPWVAIAKELGLERKTEMQAGAARPTRIGQDIAIEQASMDAADTDDHAAADAAILREEREETLRRIRKLAESELPKAKESAKALIDSFNEGEMTDDQVRQNVAILMGCDDDFE
>NZ_CP036280.1|WP_145447314.1|2973685_2973883_-|helix-turn-helix-domain-containing-protein
MLTINQVARLLNCSTRTVYRLNDAGRMPRPVRLGALVRWNRGEIEQWIADGCPAPANPAVKGGRR
>NZ_CP036280.1|WP_145446785.1|2971349_2973689_-|DUF3987-domain-containing-protein
MSDRQQELVDTAVRYAEMGWPVFPCHPTGHQPLVDKGFYTATTDMDTIREWWGVRGRWPDAAIALRTGEESGVFVVDIDPRHGGDVLLDELEAEHGPLPHTVECQTGGGGRHIYLNWPGQRVKCSTGQVASGIDIKGDGGYVILPPSDHKSGSTYNWLLDQEPGGCAIADAPKWLLDRIAAGTDANAKHSGAVSGDEGDVIPEGNRNNTLMRLGGHLRQVGMDVVEIKVALLARNASKCQPPLDVKEVERIADSVSRYEPDSARQAYIECWPERYLGDGDADAWPDPQPIPDDLPPVKPFDPVLLPSTLRPWIVDIADRMQCPPDFPAVASMVALSGILGRKIAIRPKQRDNWTVYPNLWGVLIGRPSLMKSPPMKETLLPIRRMTADALAEYEAAMAEYLAASDLQGIQTKVIRNNIAAAMKAGEDTQDLQDELASLARPEEPKRKRYTVNDATVEALGEILAANPNGVIIERDELIGLLKSLERPGQEGARAFYLEGWTGDGSCESDRIGRGNVRIDGFCLSILGTIQPGPLGTYLGEALRGGTGDDGLMQRFQMAVWPDDPGAWQVVDRWPDSDAKNAAYAVYQRFDELPASSIGELPGAFDSNTTPFLRFDAAAQDRFYVWMVDRENHLRSGAEHPAVESHLTKYRKLLPALALSIHLAESDGGPVTLDAVTRAVGWADYLESHARRIYSRGIHPATAHARALAQRIEQGDVATGFTVRDVYHGHHWSLLADAEQVQLAVDELIELGWLRTETLNTPGRAKVVHHINAKVAAPTP
>NZ_CP036280.1|WP_145446784.1|2969661_2971137_-|tyrosine-type-recombinase/integrase
MANIFRKTYTQHLPRQCEIVERRGQRVAMWSDRRGRKHYDQITTGKQGQTKIIRVSPTWFARYRDAQGIERIESTGCRDEQAARQVLADLLRRVEHVKSGILTAEQDRQAGFADQPIARHIAAYLEHLKAKTVRGKRVSTHHRRNVKHQLERVVAECGFKRVTDISRETMETWMNQREADGMAGRTRNTHRAAIVAFCNWCVDSGRLSFNPLAKLYKADELGDRRRNRRALTEDEITRLLRSAELRPIAELGRESVAKLDDEKSGHSTWTKAKLTFDTLDAAYQCGLKLLADQPDRVDALMFVGRQRALMYRIMICSGLRKSELASITVGQAHLEGQYPSLELLAKDEKAGRGAMIPLRADLVDALHAYIDDLQARACVTALRQDTHLFPIPKDMIRVFDRDLAAASIPKRDERDRVVDLHALRHTFGTHLARAGVAPRVAMAAMRHSSLELTMNVYTDPALLDVAGAVEALPAFGSSVGEVTDQPLSVAG
>NZ_CP036280.1|WP_145446783.1|2967062_2969093_+|ammonium-transporter
MKRPMRLMGCVAGGGVSWRWLMMLPVLLLSSVALADDEAVAAVAADAVVSEAAHEVQVNLDFVWIIAASALVFLMQAGFMCLESGMSRAKNSTNVAIKNMADLLIAVVAFWAVSFGLMFGVSQSGWFGTTDFFVDVGDHPWFAAFFVFQAMFCGTAATIDSGVVAERTRFGGYCVLSLLISALIYPVFGHWAWGSFLHGGEPGWLEGMGFIDFAGSTVVNSIGAWVGLAGAIVIGARIGRFNEKGEPRKIPAHSLVMVYLGTFILFFGWFGFNCGSTLAANTDIAGIAKNTALAACFGGCASGAMSWVLSKNHLPKAEMIANVLLGGLVGITAGCAVVDAPGAAIIGIGSGIMVYFGVWFIENVLRLDDVVSAIPVHGMCGAFGTIMLAVVMPSDLLGDVSRWGQIGVQAFGVVVAFAWAFGLAFVTFKVLNAITPLRVTEEDERIGLNVAEHGASSSLLDQANAMHRATSEEELDESFKVVVEHGTEIGDLSQHFNAMVDAVREQRRRASDADGRRVADMERFRGYMAETVASIEEQTEQMSGILGTTSGHADQLNRNAVSVSDELHKLTEALHEAARSGDAGRGFAVVADAVRQLAIQSESSVSNIAEMIGSVREVSGEAAEAMGRVATTIADANSGSKSVASAIETEASHVVQVETSAKEAVTAATELREQLG
>NZ_CP036280.1|WP_145446782.1|2965887_2966826_-|hypothetical-protein
MNTKHHLVALLLIALLLPACVTNSQTTATPQATDAASNAPTPPPAKPAQPLPASERLGIVLPLTHPDARVHIPDRLLDNPPETLPVIVHFHQGFNWLSEEMHTHNINAILVFFSPGGLSSKYKMPMIENPQLFDQLLAEGLDAARAQPQLPDDITIDTITVTSFSAGFGAVREILKNPRDFDRIDHIVLADTLYAGYTGDVADKKVNPDNMVDFLRYARQAVDGNKTMIITHNSYDPPGYASTAETADYLLHHLGLQRYNVNYPVGEKLTHNTRAGKGHFEVFSSPRTDGSDHAMHLRYIGFPLAMLGLPQP
>NZ_CP036280.1|WP_145446781.1|2965126_2965861_-|DNA-repair-protein-RecO
MPRFKEQAVVLRSADWSETSQLVTLLTRDHGKVRGLAKGSKRMTPSSVARFSGGIELLTVGQILGVTRPTTELATITEWDLQDDCLHLRHSLPAQRAALYAADLTTRFIEDHDPHADLFGALLTLIDHLRNADTTQTALLNYQWSLLTEAGYRPRVDSDVHTNQPLPKRACSFDPHAGGLTHNNHDDRWRVRAQTVTLLQDLDRGEPVDTAPPESTQRANRLLAAYARELLATETETMRWLLNP
>NZ_CP036280.1|WP_145446790.1|2987025_2987316_-|CRISPR-associated-endonuclease-Cas2
MHILITYDVSTSAEGGKRRLRRVAKACLDWGQRVQASVFECKLDPGQYTRLKAALTDLINPKTDSLRFYNLGKHWHGRVEHVGRDQSSDPDAPLIV
>NZ_CP036280.1|WP_145446791.1|2987318_2988353_-|type-I-C-CRISPR-associated-endonuclease-Cas1
MKHHLNTLFVQTDGTWLRKEGQNILVCVDDETKLRVPIHTIGGVVCFGRINASTAVLTLCAEAGVAVSFLSGTGRLQARVTGFTPGNVLLRRDQYRAADDDARCLTIAGPMVAAKIANSRTTLMRGIRDHGDAEGRLAAACARMAPNAEAALSAESLDHLRGIEGEAANAYFAVLSNLVTIKSEDREAFIMQGRSKRPPRDRFNCILSFLYAMLGHDARSACEACGLDPAVGFLHRDRPGRPSLALDLMEELRSFLCDRLALSLINRRQLTRKDFEAIEGGAIRFTDQTRRTVLAAYQNRKQETIQHPYLQESTTVGLLIHLQARLLSRVLRGELDTYPAFIWR
>NZ_CP036280.1|WP_145446792.1|2988349_2989027_-|CRISPR-associated-protein-Cas4
MAGYADEDLIPISALQHYLFCPRQCALIHVDGLWAENRLTSEGKVLHERSDTPGHRTRAVEDHGVRCVRAMPLVHRRLGLTGRADVVEFPLDSEGCPAGPPRPVEHKRGNPKRLDHDRVQLAAQAICLEEMLGVEVPKGELFYHAVRRRETVTIDAHLRKVVERTVDEVRGYLETNTVPAAKQEPKCRNCSLLHLCMPAATGLSRRPGQYLIRSLRISLDTEGSP
>NZ_CP036280.1|WP_145446793.1|2989029_2989938_-|type-I-C-CRISPR-associated-protein-Cas7/Csd2
MTTATDTAITNRYDFVYFFDVLDGNPNGDPDAGNLPRIDPETGQGLVTDVCLKRKIRNFVGVEFGEQPPHEIYVKEKAVLNGQHTRAYEALKLKPEKKKLPKDQAKARELTAWMCQNFFDIRTFGAVMSTEINCGQVRGPVQLGFARSVDPLITLEHSVTRCAVTNEKDLEKERTMGRKFTIPYGLYRVHGYISPHLADPERHGTGFSEEDLELLKRALNMMFEIDHSAARGQMRPRHCFAFKHDSSLGNARADQLLSRVDYKLKPSKRDENRPARAFEDYTLETRLDDLPQGVTAETWVEP
>NZ_CP036280.1|WP_145446794.1|2989934_2991785_-|type-I-C-CRISPR-associated-protein-Cas8c/Csd1
MILPSLIDYYDRLVADPEAEVVPFGYSLQKISFCVVLNPSGKLVEIADARVPVETTGGKQKLLARQVRVAGQAKPSGSGLNPCLLWDNAAYLLGWKADDPKPERTRASFEAYRDHHLDLRKEINDEGFDAVCRFLETWDSVAFEPDEATCAYLSSFGLFRLDGERGYVHQRRGVDGWYQRTLQAQPSGAEDSTEQHAQSLISGLPRTIARLHEPKIQGVWGAQSAGATIVSFNSEASESYGKKQGHNAPVSQEEAFKYCTVLKRLLADRDRVEQIGDTTAVWWVDSPEAKVAEDVMAKAAFARFFNTFDEDSEDHDAVAAEDAADRERLKTAIQKLTRGELPDLDGVDEGFHVLGLSPNAARLSVRFWWSGPLRDMLERVAQHHADARLLPVPPREQGRPMTIFRVLQATARHDGTPPKPDAKAIAHKLAGEVARSVFSGGPYPQSLLEAIVRRVRTDGVITHTRAAIVKACITRRRRVLAGPGGRFQEVPVSLNPDGPGPYQLGRLFAVLEKTQTDALPGTNRTIREGYFSSASATPAAVFPRLLRLSQHHLAKLDPGFKTNREKLIQEVCSHLETFPKQLKLEEQGLFQIGYYHQRQDLFTKKSETPVSEETSE
>NZ_CP036280.1|WP_145446795.1|2991781_2992504_-|type-I-C-CRISPR-associated-protein-Cas5
MAQHGVRLRVWGPTACFARPEMKVEAVSYDVMTPSAARGIVEAIYWKPEIRWVITAIHVLSPIRFMSLRTNGVASKIPAKGAVGSAMKKGSGAIALYADEDRQQFAAQVLRDVHYIIEARFETLSGSDNAGKHLGMFQRRADSGQCFHRPYLGRREHEAFFAWVDPETTVPAPSEPLPADWTTEPYPVIAQADRASLSGERDLGYMLWDIDHPSDRTPHFFKAVLRDGVIRDIDQERRLA
>NZ_CP036280.1|WP_145446796.1|2992503_2994789_-|CRISPR-associated-endonuclease-Cas3''
MRQRNCYAHTKEGVRPEDGWEPVLEHLKRVAYGIEGCFPGAQAAAEIFRTSAWGEYLALTHDLGKYADGYQDYLLEATDEDRAQAPTRVDHSSFGALLAEKQRPFGTLLAQAIAGHHGGMPDYQELVDRLRRKQDLTAPYAPRELLELEVPELPPLQHISKGRDDKAFQLAFLVRMTFSALVDADFLATEWFMSPERALRRGRVMPPSLNALRRALDEHLSGLANNASPTELNRHRQQILQACRTRAEEKPGLFSLTVPTGGGKTLSSLAFGLEHATRHGLRRVIYAIPYTSIIEQNAEVFRGALASAGEGAVLEHHANFEPSEEDTWSRLASENWDAPLIVTTNVQMFESLFHNRPGRCRKLHHLADSVIILDEAQMLPVNLLKPTLMALNELVQNYGCTVVLCTATQPAIHWRQDEFEIGLEGVREIIPEPKTLAQALRRVTIEPVRTLTQDALAMELADLDRVLCVVHTKKQARELYKQLVERLTKEDDDASCFFLTTDLCAEHRTSVLQQIRERLEAEQPCRVVSTSLVEAGVDIDFPVVYRAIAGLDSIAQASGRCNREGKLPEPGRVVVFDTGEQPPAYARQAADDARAVMRQHKDLLSPRAIEAYFREHYWQNQDRWDHGARDRNGVKGPVMSCFSFDGSNMVLNFRTAAERYQLITDSTTPVVVPWNDVGRLLVDELRSLKYPADHSLMRRCQRLAVQVRSHALKSMLADGVIEEPPMARGIYILKYQQAYDPVLGLHPGAGMNPEWLIEGGV
>NZ_CP036280.1|WP_145446797.1|2995157_2996132_-|hypothetical-protein
MTTEFRVSGVCERDIDLLLLEELAASQDFLQWFVQRTTRLHGTCELLRIGRSITQSNGESDLELLLRFEHGDKHKILIENKVDASFQKDQAARYAERSANYLDRDELRTCTTVLIAPDDYLAGCSETEFDETLSYESIVDWLENNDPSLRTAYKVYLLKTAIEKAHVGYNMIEDQSVTKFWKGYWQVASRVTPELEMPHPGGKPATSSFIHFRPLNRPAGTHIIHKCCSGAIDLQLNGLGRRVGEVASRLEPCLEEGMQVVRTQKSAAVRIQQEIIDFAKPFDQSAQAAERGMRAAVHLLYWAREHNEALQSVMAEGSEGETGP
>NZ_CP036280.1|WP_145446798.1|2996190_2997177_-|WYL-domain-containing-protein
MPADYSKVHRLLLEIMLMQQGNAGNADDLAQRCDVEVRTIYRDLKVISDLSIPYFFDEEARTYRIRKDFFLPPVHMTAPESLALVALAGQIAGQDQIAMTSPAASAIEKLRSQLPESVLGEVEGLEPHIEIRLPATGPDEGAVKDVFTVMQGAIRRSVEVVCTYESATTDSDNGGEAFRLRPYALSFDQRAWYVVGHHSGRDAVRRLKLNRFTEARPTETAFTRPENFSLTSFRGNAWRMIRGETTYAVEILFDATVADAVSETTWHRTQEIEEHEDGSLTFRCTVDGLDEIVWWVLGYGPHAKVKQPDDLVERLRDLAERTAEQYRS
>NZ_CP036280.1|WP_145446799.1|2997249_2999130_-|hypothetical-protein
MNSGNPRAIAALRVLTLLTLLSTNTLAENNTLPGYAGIWYGLGTPGPYGYKYSGGLGTYPQQHGTLATYAHQVNRTYFVYGSDSPDGLASAISYYDHTTGLLARPRVLTVPGGDDAHNNPTMTILEDGRLFVADNAHGFSRDSSFLISEQPWDISAFTTTLSLTRSGANFSYGNPYTIPGQGVLFLHTHYDLPPDGAERNLYWNTSPDGITWDHKWNLNLFPDHHRPLLSNLEKGQYQVSSQYGNVVGTAFNMHPASSPNGSGLNARTNLYYLQTPDAGRTWTAANGATVQTPLTDTINPALVAEYASAGLNVYLKQTTFDTQGNPVLVYLTADDYSPGPDRFDRTLHTARWTGSTWDIRDVLTTDHNYDQGSMVITQAEDGSEIWSILGPYLDGSSPWRTGGDLGYWQSDDLGQTWQLSRQPLPDAATHHTYVRNVNKAQDAFAFLWADGDPDTFSTSHLYFANADATRVYRMPLSMEHDFALPELVWAEEGCWPEPGDLNGDGVINANDIDSFIYATCASSGDLDTDGQVSQYDLDHLVTSILGTTFGDANLDRRVDLLDLSQLAASFGQTGGWADGDFDLNGIVNLNDLSILAANFGFDGTAVPEPSIPVLVAIMGLQRRRRL

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Crispr_ID: NZ_CP036280_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036280_9

3037883-3037998

Orphan

Consensus_repeat	Method
GAAGTTAGCGGCGAGGATCGAGAGGTCGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP036280_9

>merge|NZ_CP036280|9|3037883-3037998|CRISPRCasFinder
GAAGTTAGCGGCGAGGATCGAGAGGTCGAGCAGGTCGACGACGCCGTCGACGTTGAAGTCGCCCTGCTCGAAGGTGCCGAACGAGTCGAAGTTGGCGGCGAGGATCGAGAGGTCGA

>NZ_CP036280|9|9|3037883-3037998|CRISPRCasFinder
GAAGTTAGCGGCGAGGATCGAGAGGTCGA	GCAGGTCGACGACGCCGTCGACGTTGAAGTCGCCCTGCTCGAAGGTGCCGAACGAGTC
GAAGTTGGCGGCGAGGATCGAGAGGTCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036280.1\|WP_145446834.1\|3045351_3046107_-\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|277317
NZ_CP036280.1\|WP_145446836.1\|3047392_3048715_+\|DUF4349-domain-containing-protein	unknown	unknown	gnl\|CDD\|379526
NZ_CP036280.1\|WP_145446826.1\|3033705_3034572_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|225117
NZ_CP036280.1\|WP_145446830.1\|3040412_3041084_-\|HAD-IA-family-hydrolase	unknown	unknown	gnl\|CDD\|223710
NZ_CP036280.1\|WP_145446820.1\|3024833_3027548_+\|response-regulator	unknown	unknown	gnl\|CDD\|274362
NZ_CP036280.1\|WP_145446827.1\|3034683_3035853_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP036280.1\|WP_145446835.1\|3046109_3047366_+\|glycosyltransferase-family-9-protein	unknown	unknown	gnl\|CDD\|340821
NZ_CP036280.1\|WP_145446824.1\|3031385_3032159_-\|3-ketoacyl-ACP-reductase	unknown	unknown	gnl\|CDD\|237188
NZ_CP036280.1\|WP_145446832.1\|3042855_3044046_-\|phosphoglycerate-kinase	unknown	unknown	gnl\|CDD\|234613
NZ_CP036280.1\|WP_145446821.1\|3027554_3029654_+\|response-regulator	unknown	unknown	gnl\|CDD\|225971
NZ_CP036280.1\|WP_145446831.1\|3041835_3042825_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446829.1\|3039398_3040229_+\|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl\|CDD\|224007
NZ_CP036280.1\|WP_145446822.1\|3029660_3030704_-\|sugar-kinase	unknown	unknown	gnl\|CDD\|238571
NZ_CP036280.1\|WP_145447320.1\|3041096_3041771_-\|ribulose-phosphate-3-epimerase	unknown	unknown	gnl\|CDD\|238244
NZ_CP036280.1\|WP_145446823.1\|3030728_3031364_-\|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	unknown	unknown	gnl\|CDD\|188632
NZ_CP036280.1\|WP_145447316.1\|3035909_3036695_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|366542
NZ_CP036280.1\|WP_145447318.1\|3036799_3037771_+\|twin-arginine-translocation-signal-domain-containing-protein	unknown	unknown	gnl\|CDD\|381326
NZ_CP036280.1\|WP_145446837.1\|3048714_3049683_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|234574
NZ_CP036280.1\|WP_145446825.1\|3032155_3033568_-\|glycosyl-hydrolase	unknown	unknown	unknown
NZ_CP036280.1\|WP_145446833.1\|3044146_3045355_+\|aminomethyl-transferase-family-protein	unknown	unknown	gnl\|CDD\|223481

Protein	Function_ID	Function_description	E-value
NZ_CP036280.1\|WP_145446834.1\|3045351_3046107_-\|metallophosphoesterase	gnl\|CDD\|277317	cd00838, MPP_superfamily, metallophosphatase superfamily, metallophosphatase domain. Metallophosphatases (MPPs), also known as metallophosphoesterases, phosphodiesterases (PDEs), binuclear metallophosphoesterases, and dimetal-containing phosphoesterases (DMPs), represent a diverse superfamily of enzymes with a conserved domain containing 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. This superfamily includes: the phosphoprotein phosphatases (PPPs), 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.	2.18637e-15
NZ_CP036280.1\|WP_145446836.1\|3047392_3048715_+\|DUF4349-domain-containing-protein	gnl\|CDD\|379526	pfam14257, DUF4349, Domain of unknown function (DUF4349). This family of proteins is found in bacteria and archaea. Proteins in this family are typically between 282 and 353 amino acids in length. There is a single completely conserved residue D that may be functionally important.	2.76536e-49
NZ_CP036280.1\|WP_145446826.1\|3033705_3034572_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	6.43584e-30
NZ_CP036280.1\|WP_145446830.1\|3040412_3041084_-\|HAD-IA-family-hydrolase	gnl\|CDD\|223710	COG0637, COG0637, Predicted phosphatase/phosphohexomutase [General function prediction only].	1.6225e-49
NZ_CP036280.1\|WP_145446820.1\|3024833_3027548_+\|response-regulator	gnl\|CDD\|274362	TIGR02956, sensor_protein_TorS, TMAO reductase sytem sensor TorS. This protein, TorS, is part of a regulatory system for the torCAD operon that encodes the pterin molybdenum cofactor-containing enzyme trimethylamine-N-oxide (TMAO) reductase (TorA), a cognate chaperone (TorD), and a penta-haem cytochrome (TorC). TorS works together with the inducer-binding protein TorT and the response regulator TorR. TorS contains histidine kinase ATPase (pfam02518), HAMP (pfam00672), phosphoacceptor (pfam00512), and phosphotransfer (pfam01627) domains and a response regulator receiver domain (pfam00072). [Signal transduction, Two-component systems].	3.6371e-100
NZ_CP036280.1\|WP_145446827.1\|3034683_3035853_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	3.26227e-50
NZ_CP036280.1\|WP_145446835.1\|3046109_3047366_+\|glycosyltransferase-family-9-protein	gnl\|CDD\|340821	cd03789, GT9_LPS_heptosyltransferase, lipopolysaccharide heptosyltransferase and similar proteins. Lipopolysaccharide heptosyltransferase (2.4.99.B6) is involved in the biosynthesis of lipooligosaccharide (LOS). Lipopolysaccharide (LPS) is a major component of the outer membrane of gram-negative bacteria. LPS heptosyltransferase transfers heptose molecules from ADP-heptose to 3-deoxy-D-manno-octulosonic acid (KDO), a part of the inner core component of LPS. This family also contains lipopolysaccharide 1,2-N-acetylglucosaminetransferase EC 2.4.1.56 and belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	8.13288e-58
NZ_CP036280.1\|WP_145446824.1\|3031385_3032159_-\|3-ketoacyl-ACP-reductase	gnl\|CDD\|237188	PRK12745, PRK12745, 3-ketoacyl-(acyl-carrier-protein) reductase; Provisional.	2.10698e-131
NZ_CP036280.1\|WP_145446832.1\|3042855_3044046_-\|phosphoglycerate-kinase	gnl\|CDD\|234613	PRK00073, pgk, phosphoglycerate kinase; Provisional.	0
NZ_CP036280.1\|WP_145446821.1\|3027554_3029654_+\|response-regulator	gnl\|CDD\|225971	COG3437, COG3437, Response regulator containing a CheY-like receiver domain and an HD-GYP domain [Transcription / Signal transduction mechanisms].	2.21886e-98
NZ_CP036280.1\|WP_145446829.1\|3039398_3040229_+\|sugar-phosphate-isomerase/epimerase	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	8.8014e-10
NZ_CP036280.1\|WP_145446822.1\|3029660_3030704_-\|sugar-kinase	gnl\|CDD\|238571	cd01166, KdgK, 2-keto-3-deoxygluconate kinase (KdgK) phosphorylates 2-keto-3-deoxygluconate (KDG) to form 2-keto-3-deoxy-6-phosphogluconate (KDGP). KDG is the common intermediate product, that allows organisms to channel D-glucuronate and/or D-galacturinate into the glycolysis and therefore use polymers, like pectin and xylan as carbon sources.	8.3757e-90
NZ_CP036280.1\|WP_145447320.1\|3041096_3041771_-\|ribulose-phosphate-3-epimerase	gnl\|CDD\|238244	cd00429, RPE, Ribulose-5-phosphate 3-epimerase (RPE). This enzyme catalyses the interconversion of D-ribulose 5-phosphate (Ru5P) into D-xylulose 5-phosphate, as part of the Calvin cycle (reductive pentose phosphate pathway) in chloroplasts and in the oxidative pentose phosphate pathway. In the Calvin cycle Ru5P is phosphorylated by phosphoribulose kinase to ribulose-1,5-bisphosphate, which in turn is used by RubisCO (ribulose-1,5-bisphosphate carboxylase/oxygenase) to incorporate CO2 as the central step in carbohydrate synthesis.	4.39967e-87
NZ_CP036280.1\|WP_145446823.1\|3030728_3031364_-\|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase	gnl\|CDD\|188632	cd00452, KDPG_aldolase, KDPG and KHG aldolase. KDPG and KHG aldolase. This family belongs to the class I adolases whose reaction mechanism involves Schiff base formation between a substrate carbonyl and lysine residue in the active site. 2-keto-3-deoxy-6-phosphogluconate (KDPG) aldolase, is best known for its role in the Entner-Doudoroff pathway of bacteria, where it catalyzes the reversible cleavage of KDPG to pyruvate and glyceraldehyde-3-phosphate. 2-keto-4-hydroxyglutarate (KHG) aldolase, which has enzymatic specificity toward glyoxylate, forming KHG in the presence of pyruvate, and is capable of regulating glyoxylate levels in the glyoxylate bypass, an alternate pathway when bacteria are grown on acetate carbon sources.	5.26449e-71
NZ_CP036280.1\|WP_145447316.1\|3035909_3036695_+\|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.	8.84024e-32
NZ_CP036280.1\|WP_145447318.1\|3036799_3037771_+\|twin-arginine-translocation-signal-domain-containing-protein	gnl\|CDD\|381326	cd19100, AKR_unchar, uncharacterized aldo-keto reductase (AKR) superfamily protein. This family includes a group of uncharacterized AKR superfamily proteins. Aldo-keto reductases (AKRs) are a superfamily of soluble NAD(P)(H) oxidoreductases whose chief purpose is to reduce aldehydes and ketones to primary and secondary alcohols. AKRs are present in all phyla and are of importance in both health and industrial applications.	7.10733e-70
NZ_CP036280.1\|WP_145446837.1\|3048714_3049683_+\|hypothetical-protein	gnl\|CDD\|234574	PRK00015, rnhB, ribonuclease HII; Validated.	1.55831e-06
NZ_CP036280.1\|WP_145446833.1\|3044146_3045355_+\|aminomethyl-transferase-family-protein	gnl\|CDD\|223481	COG0404, GcvT, Glycine cleavage system T protein (aminomethyltransferase) [Amino acid transport and metabolism].	4.94042e-38

>NZ_CP036280.1|WP_145447318.1|3036799_3037771_+|twin-arginine-translocation-signal-domain-containing-protein
MSHDSRRDFLKKAALGGALAAGLTQGRSARADDQPDRRVVPRTTLGKTGREVSILGLGLGSAYTRPYENDPETAQALLEAALDHGINYFDTARAYGPSEQMIAPVVKAHRDRIYLVSKSGARDYDGLMREFEITTTNLGVDRLDLYHLHNLKPGQDDLGRMERGCLRAIRELREQGAIGHFGVTGHSGAQIMTDAIERFDPDAVLTIFPVSRPDQGRYETQTLAVARQKKMGVIAMKIFRRAREADLQASKMVSYALSLPGVHTAIIGLDRLDHLIDNVNTVTNLEPMDEAERDELHRIAKARLGNDPAPYELAGYRDAHDVA
>NZ_CP036280.1|WP_145447316.1|3035909_3036695_+|TIM-barrel-protein
MTNKPWSLAECCDRYAAAGFGGISVWRNVIEPIGVDEAARIVKGSGLSVPALVRGGFFVSADNAKRQAATDDNKRCIDEAAALGAEMVVLVVGAEPGTPLDEARRQVAEGIGACMDHARANSVRLAIEPLHPMYAADKSCVNRIAEAREICATLGDPLVGVAVDVYHVWWDPDLATEIELLGREDRLFGFHVCDWRVNTRHLLTDRGLMGEGCIDIARIRAMVEKAGFTGLNEVEVFSEEHWAEDQDAYLATIADACLKRS
>NZ_CP036280.1|WP_145446827.1|3034683_3035853_+|Gfo/Idh/MocA-family-oxidoreductase
MEQRRLGVILSGVTGRMGTNQHLIRSVLAIIKQGGVKVSPELTLMPDPILVGRNENKLRALAEAHGPDAIGKPLRHTTDLDAVLASKDEEIFFDASLTQLRGNFVGKAIEAGKSIYCEKPTATTTAEALALAEKAERAGVKNGVVQDKLWLPGIRKLKMLIDQGFFGKILSVRGDFGYWVFTGEVDDQPAQRPSWNYREEDGGGIMVDMFCHWRYVIDNVFGPVASLVAHGNVDLDSRVDESGKAYKATADDSAYGIFLLEDGTVCQFNSSWCSRVRRDDLLTIQVDGTHGSAVAGLRECWVQPIAATPKPVWNPDIPQPIDFTANWSQVPNATEYDNAFKIQWEMFLRHVALDEPFRWSLREGAKGVQLAELGLQSWKNRQWVDVKPI
>NZ_CP036280.1|WP_145446826.1|3033705_3034572_+|helix-turn-helix-domain-containing-protein
MIRASAIETMSPEQAVLDACSRLFRREDAVADVLVRRLHGPIEVAPHMHREGVQFVLLRRCGGRVCVQGNWLGVSGTTLLVSYPGDRHGYELKPSSARSEMVVVKLAMDPHWPAARHRPWPDIVASGEESPRLTDAIDRLQRDVRPVGPSVPLWVADAAGVLCAWPRTDQPGITQAHSEDEDPAIQAALSLIEEHPEAPPSLAQMASVAHLSPRQFTRRFERAVGRTPHAYVNERRIERAKALLFDDRVSGEQVARALGFSSQATFTRWFRQHTGRTPMQYRTDPGVL
>NZ_CP036280.1|WP_145446825.1|3032155_3033568_-|glycosyl-hydrolase
MIHVDTQIEPSTLLPAIERMWALSADKIRAIEQSFPPGSPSPVFTVAGQYSAQGWTEWTQGFQYGAAALQFDATGDTEFLDLARDRTRQVMAPHLTHTGVHDHGFNNVSTYGNLWRLAKEHRFEASADEIDFYELALKVTGAVQASRWSTTADGTGYIYSFNGPQSLFVDTIRSCRALAVSHQLGHVLQGERDARISLLGRIIEHARNTARYNIWYGPDSENGPRDTYDVRGRTAHESVFNTNNGDYRCPSTQQGYSAFSTWTRGLAWAMLGYPEQLEFIQTLADDQLEPFGGRDAITAFMLEAARATCDFYIEQTPVDGVPYWDTGAPGLAKMGDYLDRPAEPLNDHEPVDSSAAAIGCQGLIRLGIYLKDSDPQAAGRYLKAGLTSLQSLLTDTYLGTDPGHQGLLLHTVYHRPNGWDHIPEGCSIPCGEAAMWGDYHLREAALTVQRLANNQTPYTFFGPVEKGGAT
>NZ_CP036280.1|WP_145446824.1|3031385_3032159_-|3-ketoacyl-ACP-reductase
MSRPVALVTGGSRGIGLGIARRLASDGYDLVINGRRPQADVQPVIDELTSLGVDVLYVAADIASLDDHERLVQAIDERFGRLDALINNAGVAPNERADIREATAESFDRLISINLRGPYFLTQRVANWMIQQKQADDTRTPSITFVTSISSTVVSVNRGDYCLSKAALSMAAQLWAARLGEFGIPCYEVRPGIIQTDMTSGVTEKYDKLFAEGIAIDRRWGKPEDVGSVVAALVRGDLPYATGQAIMVDGGLTTQRL
>NZ_CP036280.1|WP_145446823.1|3030728_3031364_-|bifunctional-4-hydroxy-2-oxoglutarate-aldolase/2-dehydro-3-deoxy-phosphogluconate-aldolase
MSREAILQRLEKERIVAVVRLKAAEDMPALAEALAAGGVRAIEVTLTTTNAIECIRDLDKRFGDELFIGVGSVLTTDDATAAVEAGAKYVVSPVFDPAVIDAAHAANAAAMPGCFTPTEIHRATQAGADVVKVFPADVVGIPFFKAVRAPMPHLRMMPTGGVTLDNAGEWIAAGAIAVGAGSALCSKAALESKDWAAITANAQRIRASADA
>NZ_CP036280.1|WP_145446822.1|3029660_3030704_-|sugar-kinase
MPASPVRVVTFGEIMLRLSTPGFSRFLQTDRFDAVYGGGEANVAASLAQFGLDAAFLSKLPSHEIGQAAVNHLRRFGVDTGLIVRGGDRVGIYFLETGASQRPSKVVYDRANAAVTTLEPAEIDPDAIFKNASWFHWTGITPALGEKPRATLAKLLEAAQRAGCTVSCDLNFRKKLWTTDQAQAVMRPLMEHVDVCIANEEDAEKSLGIKPDDTDVTAGHLDEAGYGRLAQTLKDQFSFSTVAITLRESHSASRNGWSALMLDDKDCSTPTRSRVYDIQLVDRVGGGDSFAAGLIYGLNTLATTREALEFAVAASCMKQTIPGDFNILSADEVLKLAGGDASGRVDR
>NZ_CP036280.1|WP_145446821.1|3027554_3029654_+|response-regulator
MDQPAPEPEAITSNDRVLLVDDNPVNLDVLAQSLEARGLELLIARSGEEALVVAASAKPAVILLDINMPGIGGFETCRRLKADTSTADAVVVFLSARDAVEDRVQGLELGAADYIAKPFQVEEVQARVARQIALYHERRELKTRAADKDPASEERFRAIDPASLRAMIEAGESDRFELKSTLRWNLKSDKAGKEIEDAWLKTVVAFLNTDGGVLVVGVDDDGNALGIEADRFDNADRYLLHVNNLIRQHVGAAYMHFIRFDLVPIDDKQVLAMRVLPAAEPAFLRRNNDELFFIRVGPGSRKLTASEMVAYIQNRREDQTREVVPAEPTRVETAPESQERAPDRILLVDDNTTNLQVLFQTLSDQDYELLVARSGEEAIEVATAGSPTLILLDIMMPPGIDGYETCKRLRQKPETADVAVIFMSALQDTDARVRGFEVGAVDYITKPFQADEVIARVRTHLTIQKLQRSLSAANSELQRFNADLEDRVAERSAQLVKSRDAIIFGLAKLAESRDDDTGRHLERICRYVRILSEELAREDPGIETSWVESVAVTAALHDIGKVAIPDAILLKPGRLSDEERSRMQEHAKIGSGTLSAIRERWGSSQFLTTAIEIAHHHHERWDGSGYPDGLAGEAIPLPARIVAVADVYDALRSKRVYKPAMTDDEAAQEIINASCTQFDPRVVEAFGRVRDEFRRVLEG
>NZ_CP036280.1|WP_145446820.1|3024833_3027548_+|response-regulator
MRFSSSLSGRILLLGILPTVVILTALILALAVSGVRRLHEQSLEALELLANEVATQISHTNEHAGLGTIMMAQAQQAALFGQRETSVEFAREVLDRFPQLNGVSFVYEPDADGQDALWVGGAGPLAAGMDDRGRFLPYWSRGENGSLVLAGVSDPDARPGYAEAKRWYEQEGEIRAVMGEPVRLGDKMLIELTYPIIVDGRFVGAATIDRSLTTIRALLERIKTDASVDIFVISGEHRFVAATTAERELLKTQPVDETAYHKLFSREALIGGIEGMYDPYDGEAYYFATSQVRAGGWTLVVRESRSAIVDPIRVDFTVIVSTVVVALLAVLSLSMWILRHTSTRIRRAVEVADQLARRDLSGDLDLRSTSRDEVTQLGESFQSLVATMRETEAFVGAVAEGDFSRTFEQRSEADNLARSINAMSRMRQEAEAALREARLEAEQANVAKSVFLANMSHELRTPLNGVLGYVQILLRDRSLNEQQRRSLDAIMNSGEHLLMLINDILDLSKIEAGRLEVDLAACDLHKLLQSVEDVLAHRAKSKSLAFEVDVAAEVPRGIRTDATKLKQVLVNLAGNAVKFTEAGSVTISVGETEDKRLRFSVRDTGIGMSEEELAGIFDAFKQAAAGKDAGGTGLGLTISRRLVLALGGVLSVESRPGAGSTFSFTHPLEEVDEDALSLEQTASLAGHASLSLPEVQRRTVLVVDDREANREILDHALRGVGFATEIAENGREALDVLEKTPVDAVLMDVRMPVMNGIEATERLRADERFRDLPVIAVSASVFPNQQKKFREAGCSDFLAKPVRLNELFEKLAHHLGLTYTTEDAAEEPMRATTSEPLSAERAGEVVGPLREALRVRSFTALNALAERLAADEATASVAERIRSATRGFDFDALDRLADELERGD
>NZ_CP036280.1|WP_145446829.1|3039398_3040229_+|sugar-phosphate-isomerase/epimerase
MELQIFRHLWGVPDPLDVCIPRFVKAGYDGIECASAEKLPQGVTTDDLRGAIETHNLAYLAQTFTTGDSVAEHVASFRAELDRVLPLNPVRIGCHSGWDRFPLKDAIDLYRELVRIEADLGIPVGHETHRSRIFYNPWTTRDVLMEVPEVKLVCDFSHWVCVCERIPEEPEVFALAADRCMHLHARIGYAEGPQVTDPDAPEFAAERAAHEAWWQQIWAVQQERGESVTTVTPEFGPPPYLHTLPHTQEPVADLEDVCDRQAGNVRRLFAAWSSRA
>NZ_CP036280.1|WP_145446830.1|3040412_3041084_-|HAD-IA-family-hydrolase
MLEGIVFDFDGLILDTEGPQYDGWRSVYERFGLDLPIDRWVEVLGRPAWMFDFHTRLEELGDPAYDREAIDAERRKSVRSRIDASDLMPGVRDLVAQARSKGLRLSIASGSDREWVAGYLEKHGLIDAFPILVTREETTRHKPEPDPFAEACRRMGLPPQRCLALEDSPNGIRSAAAAGLYAVAVPNRVTAGQSFDEADRIVESLETVDLHEVAAAMGERVRA
>NZ_CP036280.1|WP_145447320.1|3041096_3041771_-|ribulose-phosphate-3-epimerase
MVSVSILSADFGRMAEECRDVLSRGADLLHMDVMDGHFAPNLTMGVDMIRGVRRHLPDTYLDVHLMVERPGDYVEDYAAAGANMLTFHVEVCEPLVSGGIKAKDLIKRVHDAGAEAGLVVNPPTGLDDALRVIEPVLSDIQMVLVMSVHPGRSGQKFMPEVLPKAAGLRQLAGPDLRIEMDGGLNTQTCRDAAAHGVDVMVTASALFGSDDRTAVIDAFHRSNA
>NZ_CP036280.1|WP_145446831.1|3041835_3042825_-|hypothetical-protein
MRHLLLACLILLAAGLSHARAESSLTGVMLPFRGPTNYEIEALGLVVPDAETKNGDLDTDLRVFDLGFRARFGDNPDTVPTMRIGLHTFAIDSIDPALPESAGDLFFSGGINHVLNETFTLSWGLGIGYAGELRDSDGDWSFDGGDQGIYGSAGIGLTQKIDEFSSITYLIDWDGNRSIFPDIPLPGIAYTKRLQTETPFMFTVGFPFATVRWTPVDKLNLDATFFYPESFRARIGYRVIEPLEFYGELLARNKAYAIGSLPKDRRLFFRQDLLEAGLKWRFLRGLELTVAGGWAFGQQFTTGYDVRDDTTVRKLSDAPYARLGFGMKF
>NZ_CP036280.1|WP_145446832.1|3042855_3044046_-|phosphoglycerate-kinase
MAKKTITDIDVAGKKVLMRVDFNVPLKDGAITDDRRIRMALDSIKSVLDRGGSLVLMSHLGRPKGEGAEPEFSLAPAAVRLGEMIGSEVVFASDTVGDDAKAKVAALQAGGVVLLENLRFAKAEKKGDEDFAAVLASFGDAYCNDAFGTCHRDHASMVAVPRAMKTDGKPAVCGFLVEKEIQYLSEAIGEPKRPFVAILGGAKVSDKINVIDNLLTVCDKVLIGGAMANTFALAQGYSVGKSMVEPDKVDLAKSLIEKAGDKLVLPIDAHTGDAFSADCDKQIVPADGTAEGYMALDIGPKTAKLFADLVTSAKTVVWNGPMGVFEMPPFDEGTKAVAKAVADSDSVSIIGGGDSAAAIQQLGFADQVSHVSTGGGASLEMLEGKAFNSVDLLDEK
>NZ_CP036280.1|WP_145446833.1|3044146_3045355_+|aminomethyl-transferase-family-protein
MTPLHNHLSQLGGEFLTYGPDEATAVRIPDSFGEFEAEYAAIRRRVGILVLAQQTVLQVTGEDRKDFLHRLVTQEINALEGGQTTRSLQLDTKGRVLADMLVHHGHLCTWLEMDRFHLPAVREILEQRLFTEDVELEHLDDRVFMVLIGPAALQLLAGVAEHTVETMTVESLGTMPRTTHVLTIDGVRVSATRWDMAGELAIRLAAPSDDAVAVHEKLLEAAGYEPDTEPDADFAERRRDSLRGRPIGWAAYNTARIEAGEVLFGVDFGTDCRPAEAGSRVMDETVSFTKGCYLGQEVVARMHNLGHPKRLAVGLRIDSDHLPVAGSQVLKATDDGPTLDVIGAITSSTTSPLQGGTTAAIAMMKWGQHRPGTKVYAIEVGETIEATVTEPGVDALRDKTTT
>NZ_CP036280.1|WP_145446834.1|3045351_3046107_-|metallophosphoesterase
MATALISDIHGNLDALMAVLSDIEEKGIEQIICLGDIIGYGPNPRECLDLVRDRCAWALMGNHDFAALYEPTGFNATAEAAAFWTRAELENEPDTALRRQRWEFLGNLGIRQDFENMLCVHASPRRPINEYIFPDDVITSPQKVQQIFDRIQTACLVGHTHVPGVFTDEPDFYPPSDLGGTYEFSEEEKCVINPGSVGQPRDRDPRASYAVLEGERVTFHRTEYDIDAVVAKIEKIPDLADFLGQRLLEGR
>NZ_CP036280.1|WP_145446835.1|3046109_3047366_+|glycosyltransferase-family-9-protein
MRPCQKKCSPLESSRESEHFCSSRNSPPVRPPDQELWVYSVNMAAGVQVPGPTGPRDGARLLIVRPSALGDVARTVPVLAALRGSFPNASIDWLVHPAYADAIRCHPDLREAIPFDRKGMSGFGLRPSATRKGLSLIRRLRRERYDRVYDLQGLARSGFFTWMSGSRHRVGFADAREGAAWGYNRRHHVNKVHTVDRMLGLLAADGVALQQEPDLRLYTPAEDQRWADSYLAKHGIDAERGFVCVAPTAQWRCKWWPMDRYAALINRIVAEPCCGGRVLVLAAPHEFDELLPLREALDAQAAGRVDFPPTASVGQLMGLLGRSGLVISNDSASLHLGVGLGRPVVGVFGPTDPRRVGPYGHDDAVVQPDAAREPGFTFDYRKHRDDQSLIAQIPVATVWSMILRVAGTSPDRQTSKAV
>NZ_CP036280.1|WP_145446836.1|3047392_3048715_+|DUF4349-domain-containing-protein
MKPTFAWLKIIIVLVVFVLLIGIFLPSLGAARRLAPAHEYNIYVGAGMHAADEADQARSRRPMSAGAYGIESAGIGVAMGRAYASDAPASAAPPASLKAGDVVQAMEEQSQQDPAAERQVIYTGRLIIAVADVQAAIAFVRAQAESMGGHMQSLQGEGITVRVPAQRFDSVIDRIEDLGELRHKSINAQDVTREFQDTEIQLRTARTSYDRLITLLEQAEKTEDVIAIEKELRRLKTEIDRIETRRRYLKDQVALATLTVTFNAKVPQQPTEKPIPIRWLSELAFELLNPQAPPPMNDIFRAGVTFDLPENFVRHYQEGYVTMAMAPGEVGLKVIRHNNYDEGPLEFWLSLVRDTLIDRHGVPVGEPMTEHLNGRWWGKSSTEVAVLEGTKTVAAEPHGYIVGIIAADRHVYTYEAWGPEAALATHRDAIIESMMTLRAR
>NZ_CP036280.1|WP_145446837.1|3048714_3049683_+|hypothetical-protein
MALICGIDEAGYGPLLGPLTLARVALEVPEPDADPWSLLDKAVSRTLGKRKGRLVVNDSKKLNVRSVGVVHLETSCLAFAGAADRDTTDVGLFFDGLHETSHRQLDHLPWYAPTQEQPWQPLPTALTEGELAIARSMLRTAMASAGISVRDMAVSLVFEDAFNDLVRKTHSKASASFTYVARHLMAIWRDLGQEQPVVVIDRQSGRTRYRELIAMLLPDATIRVLDESPERSAYHVREGDRSMTLGFETKADGNHFPVALASMLAKYSRELMMERLNGWFTRQLPDLTPTAGYAVDGRRFVNDITPHLPAMGIETNQICRIA

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP036280_8	8.108\|2986714\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986714-2986746	33	NZ_CP030359	Salinibacter ruber strain SP38 plasmid pSR14, complete sequence	614-646	5	0.848
NZ_CP036280_8	8.108\|2986714\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986714-2986746	33	NZ_CP030359	Salinibacter ruber strain SP38 plasmid pSR14, complete sequence	14679-14711	5	0.848
NZ_CP036280_8	8.72\|2984322\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984322-2984355	34	NC_023498	Mycobacterium phage Validus, complete genome	13115-13148	6	0.824
NZ_CP036280_8	8.11\|2980267\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980267-2980300	34	NZ_CP031166	Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence	11958-11991	7	0.794
NZ_CP036280_8	8.72\|2984322\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984322-2984355	34	MN945901	Mycobacterium phage Ximenita, complete genome	13192-13225	7	0.794
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	KY092484	Streptomyces phage Raleigh, complete genome	27106-27138	7	0.788
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	KU985096	Mycobacterium phage Kazan, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MG099952	Mycobacterium phage WunderPhul, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MK359352	Mycobacterium phage JewelBug, complete genome	1097-1131	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	KX375815	Mycobacterium phage ToneTone, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MK494090	Mycobacterium phage Jordennis, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	KX641261	Mycobacterium phage Isiphiwo, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	KF560333	Mycobacterium phage Artemis2UCLA, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	KU695582	Mycobacterium phage McFly, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MT024861	Mycobacterium phage Pmask, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MH155876	Mycobacterium phage Priamo, complete genome	1111-1145	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MK359360	Mycobacterium phage Hexamo, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MH051253	Mycobacterium phage GreedyLawyer, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MT657338	Mycobacterium phage SuperCallie99, complete genome	1097-1131	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NC_042334	Mycobacterium virus Jeffabunny, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MN728683	Mycobacterium phage Yokurt, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NC_022965	Mycobacterium phage CloudWang3, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	JF937092	Mycobacterium phage DaVinci, complete genome	1097-1131	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MF668288	Mycobacterium phage Wiks, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MH020240	Mycobacterium phage SuperAwesome, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MG099945	Mycobacterium phage Koko, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MK894433	Mycobacterium phage Kipper29, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NC_022985	Mycobacterium phage Zaka, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	JN049605	Mycobacterium virus EricB, complete genome	1097-1131	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MN586039	Mycobacterium phage Blinn1, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	MH779517	Mycobacterium phage Zulu, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NC_029077	Mycobacterium phage VohminGhazi, complete genome	1096-1130	7	0.8
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP021468	Komagataeibacter europaeus strain SRCM101446 plasmid pKE1446-1	85985-86018	8	0.765
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP021469	Komagataeibacter europaeus strain SRCM101446 plasmid pKE1446-2, complete sequence	14756-14789	8	0.765
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP004364	Komagataeibacter xylinus E25 plasmid pGX4, complete sequence	53793-53826	8	0.765
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NC_023286	Streptomyces sp. F12 plasmid pFRL6, complete sequence	84104-84137	8	0.765
NZ_CP036280_8	8.11\|2980267\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980267-2980300	34	NC_023285	Streptomyces sp. F8 plasmid pFRL5, complete sequence	330169-330202	8	0.765
NZ_CP036280_8	8.14\|2980465\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980465-2980499	35	NC_009622	Sinorhizobium medicae WSM419 plasmid pSMED03, complete sequence	145095-145129	8	0.771
NZ_CP036280_8	8.34\|2981798\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2981798-2981831	34	NZ_CP024200	Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence	270727-270760	8	0.765
NZ_CP036280_8	8.49\|2982796\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2982796-2982829	34	NZ_CP015881	Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence	1239075-1239108	8	0.765
NZ_CP036280_8	8.49\|2982796\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2982796-2982829	34	NZ_CP030263	Ensifer adhaerens strain Corn53 plasmid AA, complete sequence	934174-934207	8	0.765
NZ_CP036280_8	8.50\|2982862\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2982862-2982896	35	NZ_CP031409	Borreliella burgdorferi strain MM1 plasmid plsm_lp28-8, complete sequence	19571-19605	8	0.771
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	235228-235260	8	0.758
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP018784	Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence	323842-323874	8	0.758
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	1616860-1616892	8	0.758
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	196256-196288	8	0.758
NZ_CP036280_8	8.89\|2985452\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2985452-2985485	34	NZ_CP024792	Nostoc flagelliforme CCNUN1 plasmid pNFSY07, complete sequence	240178-240211	8	0.765
NZ_CP036280_8	8.103\|2986381\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986381-2986414	34	NZ_CP025513	Neorhizobium sp. SOG26 plasmid unnamed2, complete sequence	989760-989793	8	0.765
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NC_012811	Methylorubrum extorquens AM1 megaplasmid, complete sequence	1200607-1200640	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	1252775-1252808	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	1339199-1339232	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	1508779-1508812	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	1441702-1441735	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	1258826-1258859	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	1255563-1255596	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	1224550-1224583	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	1238261-1238294	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	1238283-1238316	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	1238283-1238316	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	1238283-1238316	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	1238283-1238316	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	1238283-1238316	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	1615886-1615919	9	0.735
NZ_CP036280_8	8.5\|2979869\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2979869-2979902	34	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	733944-733977	9	0.735
NZ_CP036280_8	8.11\|2980267\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980267-2980300	34	NC_016623	Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence	135202-135235	9	0.735
NZ_CP036280_8	8.13\|2980399\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980399-2980432	34	NZ_CP049244	Rhizobium pseudoryzae strain DSM 19479 plasmid unnamed3, complete sequence	143149-143182	9	0.735
NZ_CP036280_8	8.27\|2981333\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2981333-2981366	34	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1436825-1436858	9	0.735
NZ_CP036280_8	8.27\|2981333\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2981333-2981366	34	MH271307	Microbacterium phage OlinDD, complete genome	10946-10979	9	0.735
NZ_CP036280_8	8.27\|2981333\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2981333-2981366	34	MH271300	Microbacterium phage Hortus1, complete genome	10947-10980	9	0.735
NZ_CP036280_8	8.50\|2982862\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2982862-2982896	35	NZ_CP031409	Borreliella burgdorferi strain MM1 plasmid plsm_lp28-8, complete sequence	22652-22686	9	0.743
NZ_CP036280_8	8.64\|2983796\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2983796-2983829	34	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	421237-421270	9	0.735
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_CP022775	Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence	1479947-1479979	9	0.727
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_LR134451	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence	324549-324581	9	0.727
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_CP033873	Caulobacter sp. FWC26 plasmid p1, complete sequence	252579-252611	9	0.727
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	408699-408731	9	0.727
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	638520-638552	9	0.727
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_CP022764	Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence	1480102-1480134	9	0.727
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_CP022797	Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence	1480083-1480115	9	0.727
NZ_CP036280_8	8.71\|2984257\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984257-2984289	33	NZ_CP022758	Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence	1480066-1480098	9	0.727
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NC_019848	Sinorhizobium meliloti GR4 plasmid pRmeGR4c, complete sequence	851549-851582	9	0.735
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NC_013545	Sinorhizobium meliloti plasmid pSmeSM11a, complete sequence	122289-122322	9	0.735
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NZ_CP021796	Sinorhizobium meliloti strain USDA1157 plasmid accessoryA, complete sequence	53821-53854	9	0.735
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NZ_CP021215	Sinorhizobium meliloti RU11/001 plasmid pSmeRU11c, complete sequence	44038-44071	9	0.735
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NZ_CP019483	Sinorhizobium meliloti strain B401 plasmid pSymA, complete sequence	525642-525675	9	0.735
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NZ_CP019486	Sinorhizobium meliloti strain B399 plasmid pSymA, complete sequence	495184-495217	9	0.735
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	MN908687	Gordonia phage Skog, complete genome	80323-80355	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NC_012854	Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132505, complete sequence	266373-266405	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP050095	Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b1, complete sequence	23630-23662	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NC_008381	Rhizobium leguminosarum bv. viciae 3841 plasmid pRL10, complete sequence	247998-248030	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP020897	Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5a, complete sequence	20427-20459	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP006991	Rhizobium sp. IE4771 plasmid pRetIE4771e, complete sequence	20476-20508	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP013631	Rhizobium sp. N324 plasmid pRspN324a, complete sequence	22440-22472	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP013528	Rhizobium phaseoli strain R723 plasmid pRphaR723a, complete sequence	20437-20469	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP013581	Rhizobium phaseoli strain N261 plasmid pRphaN261a, complete sequence	20437-20469	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP030762	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed2, complete sequence	147492-147524	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP021128	Rhizobium sp. Kim5 plasmid pRetKim5d, complete sequence	22047-22079	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP054026	Rhizobium sp. JKLM12A2 plasmid pPR12A205, complete sequence	51041-51073	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	CP007645	Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803d, complete sequence	22027-22059	9	0.727
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP054036	Rhizobium sp. JKLM13E plasmid pPR13E05, complete sequence	189338-189370	9	0.727
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP025013	Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence	889223-889257	9	0.743
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP025507	Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvA, complete sequence	1057843-1057877	9	0.743
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP030761	Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence	530342-530376	9	0.743
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP054022	Rhizobium sp. JKLM12A2 plasmid pPR12A201, complete sequence	589107-589141	9	0.743
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP020331	Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence	462163-462197	9	0.743
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP022666	Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence	481380-481414	9	0.743
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP016451	Sinorhizobium sp. RAC02 plasmid pBSY16_2, complete sequence	1878-1912	9	0.743
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP050086	Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence	77294-77328	9	0.743
NZ_CP036280_8	8.11\|2980267\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980267-2980300	34	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	685790-685823	10	0.706
NZ_CP036280_8	8.11\|2980267\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980267-2980300	34	NZ_CP049358	Deinococcus wulumuqiensis R12 plasmid unnamed1, complete sequence	178449-178482	10	0.706
NZ_CP036280_8	8.11\|2980267\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980267-2980300	34	NZ_CP031159	Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdA, complete sequence	142564-142597	10	0.706
NZ_CP036280_8	8.14\|2980465\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980465-2980499	35	NC_019898	Thermobacillus composti KWC4 plasmid pTHECO01, complete sequence	31634-31668	10	0.714
NZ_CP036280_8	8.50\|2982862\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2982862-2982896	35	MK415399	CrAssphage apr34_000142F, complete genome	76047-76081	10	0.714
NZ_CP036280_8	8.67\|2983994\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2983994-2984027	34	NZ_CP016619	Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence	577-610	10	0.706
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NZ_CP048281	Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence	30733-30766	10	0.706
NZ_CP036280_8	8.82\|2984985\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984985-2985017	33	NZ_CP022568	Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK04, complete sequence	24778-24810	10	0.697
NZ_CP036280_8	8.108\|2986714\|33\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986714-2986746	33	NZ_CP023000	Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-B, complete sequence	1427449-1427481	10	0.697
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP050104	Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence	77279-77313	10	0.714
NZ_CP036280_8	8.109\|2986779\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2986779-2986813	35	NZ_CP050109	Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence	77279-77313	10	0.714
NZ_CP036280_8	8.7\|2980001\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980001-2980034	34	NC_014533	Gloeothece verrucosa PCC 7822 plasmid Cy782201, complete sequence	331631-331664	11	0.676
NZ_CP036280_8	8.14\|2980465\|35\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980465-2980499	35	NZ_CP029832	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence	16406-16440	11	0.686
NZ_CP036280_8	8.15\|2980532\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2980532-2980565	34	NZ_CP012399	Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence	495262-495295	11	0.676
NZ_CP036280_8	8.54\|2983130\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2983130-2983163	34	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	654508-654541	11	0.676
NZ_CP036280_8	8.54\|2983130\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2983130-2983163	34	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	1477874-1477907	11	0.676
NZ_CP036280_8	8.60\|2983528\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2983528-2983561	34	NZ_CP044989	Deinococcus sp. AJ005 plasmid p380k, complete sequence	370460-370493	11	0.676
NZ_CP036280_8	8.72\|2984322\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984322-2984355	34	NZ_CP040720	Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence	129577-129610	11	0.676
NZ_CP036280_8	8.74\|2984455\|34\|NZ_CP036280\|CRISPRCasFinder,CRT,PILER-CR	2984455-2984488	34	NC_019849	Sinorhizobium meliloti GR4 plasmid pRmeGR4d, complete sequence	1288543-1288576	11	0.676

1. spacer 8.108|2986714|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030359 (Salinibacter ruber strain SP38 plasmid pSR14, complete sequence) position: , mismatch: 5, identity: 0.848

ctttgccccgcccggcttcaaggt-caacgcggt	CRISPR spacer
cttcgccccgcccggattcaaggtccgaggcgg-	Protospacer
***.*********** ******** *.* ****

2. spacer 8.108|2986714|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030359 (Salinibacter ruber strain SP38 plasmid pSR14, complete sequence) position: , mismatch: 5, identity: 0.848

ctttgccccgcccggcttcaaggt-caacgcggt	CRISPR spacer
cttcgccccgcccggattcaaggtccgaggcgg-	Protospacer
***.*********** ******** *.* ****

3. spacer 8.72|2984322|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_023498 (Mycobacterium phage Validus, complete genome) position: , mismatch: 6, identity: 0.824

ccaagcggcagatcaacaacgtggtgcgcgacgc-	CRISPR spacer
tcaagtggcagttcaacaacgtggtg-acggcgct	Protospacer
.****.***** ************** .**.***

4. spacer 8.11|2980267|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031166 (Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence) position: , mismatch: 7, identity: 0.794

tgaacgagc---tcgaagcggcggagggcatcggcga	CRISPR spacer
---accggcccgtcgatgcggcggagcgcatcggcga	Protospacer
   ** .**   **** ********* **********

5. spacer 8.72|2984322|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MN945901 (Mycobacterium phage Ximenita, complete genome) position: , mismatch: 7, identity: 0.794

ccaagcggcagatcaacaacgtggtgcgcgacgc-	CRISPR spacer
tcaagtggcagttcaacaacgtggtg-acggccct	Protospacer
.****.***** ************** .**.* *

6. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to KY092484 (Streptomyces phage Raleigh, complete genome) position: , mismatch: 7, identity: 0.788

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
cggcgaggccgtcggcggtgagctgggggcgaa	Protospacer
  .********************.* *****.

7. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to KU985096 (Mycobacterium phage Kazan, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

8. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MG099952 (Mycobacterium phage WunderPhul, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

9. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MK359352 (Mycobacterium phage JewelBug, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

10. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to KX375815 (Mycobacterium phage ToneTone, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

11. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MK494090 (Mycobacterium phage Jordennis, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

12. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to KX641261 (Mycobacterium phage Isiphiwo, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

13. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to KF560333 (Mycobacterium phage Artemis2UCLA, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

14. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to KU695582 (Mycobacterium phage McFly, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

15. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MT024861 (Mycobacterium phage Pmask, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

16. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MH155876 (Mycobacterium phage Priamo, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

17. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MK359360 (Mycobacterium phage Hexamo, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

18. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MH051253 (Mycobacterium phage GreedyLawyer, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

19. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MT657338 (Mycobacterium phage SuperCallie99, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

20. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_042334 (Mycobacterium virus Jeffabunny, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

21. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MN728683 (Mycobacterium phage Yokurt, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

22. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_022965 (Mycobacterium phage CloudWang3, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

23. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to JF937092 (Mycobacterium phage DaVinci, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

24. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MF668288 (Mycobacterium phage Wiks, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

25. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MH020240 (Mycobacterium phage SuperAwesome, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

26. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MG099945 (Mycobacterium phage Koko, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

27. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MK894433 (Mycobacterium phage Kipper29, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

28. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_022985 (Mycobacterium phage Zaka, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

29. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to JN049605 (Mycobacterium virus EricB, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

30. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MN586039 (Mycobacterium phage Blinn1, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

31. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MH779517 (Mycobacterium phage Zulu, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

32. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_029077 (Mycobacterium phage VohminGhazi, complete genome) position: , mismatch: 7, identity: 0.8

--tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
ggtccctggt--ccgggaccgccgccgccgccccgtc	Protospacer
  * ** *.*  ****.************** *****

33. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021468 (Komagataeibacter europaeus strain SRCM101446 plasmid pKE1446-1) position: , mismatch: 8, identity: 0.765

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
cgggcggcagcgcgctgttcatcgccgatccgga	Protospacer
***.***************** *** *..   **

34. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021469 (Komagataeibacter europaeus strain SRCM101446 plasmid pKE1446-2, complete sequence) position: , mismatch: 8, identity: 0.765

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
cgggcggcagcgcgctgttcatcgccgatccgga	Protospacer
***.***************** *** *..   **

35. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP004364 (Komagataeibacter xylinus E25 plasmid pGX4, complete sequence) position: , mismatch: 8, identity: 0.765

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
cgggcggcagcgcgctgttcatcgccgatccgga	Protospacer
***.***************** *** *..   **

36. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_023286 (Streptomyces sp. F12 plasmid pFRL6, complete sequence) position: , mismatch: 8, identity: 0.765

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
ccgaggcgcgcgagctgttcaccgcgggcgacgt	Protospacer
* ** *   *** ******** ***********

37. spacer 8.11|2980267|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_023285 (Streptomyces sp. F8 plasmid pFRL5, complete sequence) position: , mismatch: 8, identity: 0.765

tgaacgagctcgaagcggcggagggcatcggcga	CRISPR spacer
tggccaagatcgaagcggctgagggcatcgcccg	Protospacer
**. *.** ********** ********** * .

38. spacer 8.14|2980465|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_009622 (Sinorhizobium medicae WSM419 plasmid pSMED03, complete sequence) position: , mismatch: 8, identity: 0.771

ggcggcttggcgaacagcaccgccatcgatccgca----	CRISPR spacer
gttggcttggcgaacagcatcgccagcg----gcagctc	Protospacer
* .****************.***** **    ***

39. spacer 8.34|2981798|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024200 (Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence) position: , mismatch: 8, identity: 0.765

cgcgctcgtgatactcgatgcggcgaccatccat	CRISPR spacer
ggcggatgtgatattcggtgcggcgaccatcaag	Protospacer
 ***  .******.***.************* *

40. spacer 8.49|2982796|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015881 (Ensifer adhaerens strain Casida A plasmid pCasidaAA, complete sequence) position: , mismatch: 8, identity: 0.765

ctcgctcgcctccggcatctgcctggttatcgag	CRISPR spacer
cttctccacatccggcatctggctggtcatcgag	Protospacer
**. ..*.* *********** *****.******

41. spacer 8.49|2982796|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030263 (Ensifer adhaerens strain Corn53 plasmid AA, complete sequence) position: , mismatch: 8, identity: 0.765

ctcgctcgcctccggcatctgcctggttatcgag	CRISPR spacer
cttctccacatccggcatctggctggtcatcgag	Protospacer
**. ..*.* *********** *****.******

42. spacer 8.50|2982862|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031409 (Borreliella burgdorferi strain MM1 plasmid plsm_lp28-8, complete sequence) position: , mismatch: 8, identity: 0.771

aacatcatcaccatcattaccatcacccatatata	CRISPR spacer
accctcattaccatcattaccatcaccaatagccg	Protospacer
* * ****.****************** ***  ..

43. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 8, identity: 0.758

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
gccggggcggcgctggtggcgatcgacggggcc	Protospacer
* .. ******** ************* ***

44. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018784 (Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence) position: , mismatch: 8, identity: 0.758

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
ctacgacgccgtcggcgctgagccgtgggaact	Protospacer
 .**** ********** *********** . .

45. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 8, identity: 0.758

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
gttcgaagcggtcggcggtgagccgtggctggt	Protospacer
.. ***.** ****************** .**.

46. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 8, identity: 0.758

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
gttcgaagcggtcggcggtgagccgtggctggt	Protospacer
.. ***.** ****************** .**.

47. spacer 8.89|2985452|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP024792 (Nostoc flagelliforme CCNUN1 plasmid pNFSY07, complete sequence) position: , mismatch: 8, identity: 0.765

tagtgggttggctgttaatgctaatttctggggc	CRISPR spacer
aaatgggttggctgctaatgttaatttccgacga	Protospacer
 *.***********.*****.*******.*. *

48. spacer 8.103|2986381|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP025513 (Neorhizobium sp. SOG26 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.765

gaaagcctttgcgcttttggaccgacacgccagt	CRISPR spacer
tcgcgacattgcgcttctggaccggcacgccagt	Protospacer
  . * * ********.*******.*********

49. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_012811 (Methylorubrum extorquens AM1 megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
cgggcggcagcgcgctgttcgacgcgatgcgggt	Protospacer
***.****************.*****.   . *

50. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

51. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

52. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

53. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

54. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

55. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

56. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

57. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

58. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

59. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

60. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

61. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

62. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

63. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

64. spacer 8.5|2979869|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

cggacggcagcgcgctgttcaacgcgggcgacga	CRISPR spacer
tgatcgtgcgcacgctgttcaaggcgggcgacgt	Protospacer
.*. **   **.********** **********

65. spacer 8.11|2980267|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_016623 (Azospirillum lipoferum 4B plasmid AZO_p3, complete sequence) position: , mismatch: 9, identity: 0.735

tgaacgagctcgaagcggcggagggcatcggcga	CRISPR spacer
gcggcctggtcgaagcggcgcagcgcatcggcga	Protospacer
  ..*  * *********** ** **********

66. spacer 8.13|2980399|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049244 (Rhizobium pseudoryzae strain DSM 19479 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.735

ttaaggccgatgaagcatcggtcgccgagatcaa	CRISPR spacer
tcgccatcgatgaagcgtcggttgccgagatcga	Protospacer
*..  ..*********.*****.*********.*

67. spacer 8.27|2981333|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.735

gtgctcggctggcgacacctgcccgagggtccgg	CRISPR spacer
gggctcggcttgcaacacctgcccgagctgatga	Protospacer
* ******** **.*************    .*.

68. spacer 8.27|2981333|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MH271307 (Microbacterium phage OlinDD, complete genome) position: , mismatch: 9, identity: 0.735

gtgctcggctggcgacacctgcccgagggtccgg	CRISPR spacer
gcactcggctggcgacagctgtccgagaaccgag	Protospacer
*..************** ***.*****...* .*

69. spacer 8.27|2981333|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MH271300 (Microbacterium phage Hortus1, complete genome) position: , mismatch: 9, identity: 0.735

gtgctcggctggcgacacctgcccgagggtccgg	CRISPR spacer
gcactcggctggcgacagctgtccgagaaccgag	Protospacer
*..************** ***.*****...* .*

70. spacer 8.50|2982862|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031409 (Borreliella burgdorferi strain MM1 plasmid plsm_lp28-8, complete sequence) position: , mismatch: 9, identity: 0.743

aacatcatcaccatcattaccatcacccatatata	CRISPR spacer
acccgcatcaccatcattaccaccaccaatagccg	Protospacer
* *  *****************.**** ***  ..

71. spacer 8.64|2983796|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 9, identity: 0.735

ctacgcgtttcggcagggcgtggacgatgcaaaa	CRISPR spacer
cgccgcgttccagcagggcgtggacgatgtcgcg	Protospacer
*  ******.*.*****************. . .

72. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022775 (Ralstonia solanacearum strain T12 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
gcgagagcgtcgcaggtgccgatcgaccggatc	Protospacer
*  * .*** ******** ***********.

73. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LR134451 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
aagatggtggcgaaggtggcgatcgacgcgatc	Protospacer
.* ****.**** **************  *.

74. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP033873 (Caulobacter sp. FWC26 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
gtgatggcggtgcaggtggggatcgacggtcac	Protospacer
*  *******.******** ******* *  .

75. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
ccattggcggcgcagctggcgatctacctcggc	Protospacer
    *********** ******** ***  **

76. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
ccattggcggcgcagctggcgatctacctcggc	Protospacer
    *********** ******** ***  **

77. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022764 (Ralstonia solanacearum strain T82 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
gcgagagcgtcgcaggtgccgatcgaccggatc	Protospacer
*  * .*** ******** ***********.

78. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022797 (Ralstonia solanacearum strain SL2312 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
gcgagagcgtcgcaggtgccgatcgaccggatc	Protospacer
*  * .*** ******** ***********.

79. spacer 8.71|2984257|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022758 (Ralstonia solanacearum strain T101 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.727

gatatggcggcgcaggtggcgatcgaccgggga	CRISPR spacer
gcgagagcgtcgcaggtgccgatcgaccggatc	Protospacer
*  * .*** ******** ***********.

80. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_019848 (Sinorhizobium meliloti GR4 plasmid pRmeGR4c, complete sequence) position: , mismatch: 9, identity: 0.735

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
ttccaatctcggtagccgcacccgtcgctgcaat	Protospacer
** *.*******************. .*.** .

81. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_013545 (Sinorhizobium meliloti plasmid pSmeSM11a, complete sequence) position: , mismatch: 9, identity: 0.735

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
ttccaatctcggtagccgcacccgtcgctgcaat	Protospacer
** *.*******************. .*.** .

82. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021796 (Sinorhizobium meliloti strain USDA1157 plasmid accessoryA, complete sequence) position: , mismatch: 9, identity: 0.735

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
ttccaatctcggtagccgcacccgtcgctgcaat	Protospacer
** *.*******************. .*.** .

83. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021215 (Sinorhizobium meliloti RU11/001 plasmid pSmeRU11c, complete sequence) position: , mismatch: 9, identity: 0.735

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
ttccaatctcggtagccgcacccgtcgctgcaat	Protospacer
** *.*******************. .*.** .

84. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP019483 (Sinorhizobium meliloti strain B401 plasmid pSymA, complete sequence) position: , mismatch: 9, identity: 0.735

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
ttccaatctcggtagccgcacccgtcgctgcaat	Protospacer
** *.*******************. .*.** .

85. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP019486 (Sinorhizobium meliloti strain B399 plasmid pSymA, complete sequence) position: , mismatch: 9, identity: 0.735

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
ttccaatctcggtagccgcacccgtcgctgcaat	Protospacer
** *.*******************. .*.** .

86. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MN908687 (Gordonia phage Skog, complete genome) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
caccgaggccgacggcggtgagtcgtggggtca	Protospacer
   ******** **********.******

87. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_012854 (Rhizobium leguminosarum bv. trifolii WSM1325 plasmid pR132505, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

88. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050095 (Rhizobium leguminosarum bv. trifolii strain 22B plasmid pRL22b1, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

89. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_008381 (Rhizobium leguminosarum bv. viciae 3841 plasmid pRL10, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

90. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020897 (Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5a, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

91. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP006991 (Rhizobium sp. IE4771 plasmid pRetIE4771e, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggtcct	Protospacer
 ********** *.***********. **.  .

92. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013631 (Rhizobium sp. N324 plasmid pRspN324a, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

93. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013528 (Rhizobium phaseoli strain R723 plasmid pRphaR723a, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

94. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013581 (Rhizobium phaseoli strain N261 plasmid pRphaN261a, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

95. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030762 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

96. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021128 (Rhizobium sp. Kim5 plasmid pRetKim5d, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggtcct	Protospacer
 ********** *.***********. **.  .

97. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP054026 (Rhizobium sp. JKLM12A2 plasmid pPR12A205, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

98. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to CP007645 (Rhizobium etli bv. phaseoli str. IE4803 plasmid pRetIE4803d, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggtcct	Protospacer
 ********** *.***********. **.  .

99. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP054036 (Rhizobium sp. JKLM13E plasmid pPR13E05, complete sequence) position: , mismatch: 9, identity: 0.727

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctggttct	Protospacer
 ********** *.***********. **.  .

100. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP025013 (Rhizobium leguminosarum strain Norway plasmid pRLN1, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
tgccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*********.*** *************  .  *.

101. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP025507 (Rhizobium leguminosarum bv. viciae strain UPM791 plasmid pRlvA, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
tgccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*********.*** *************  .  *.

102. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP030761 (Rhizobium leguminosarum strain ATCC 14479 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
tgccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*********.*** *************  .  *.

103. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP054022 (Rhizobium sp. JKLM12A2 plasmid pPR12A201, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
tgccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*********.*** *************  .  *.

104. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP020331 (Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
cgccggatcgccgtaaccgccgccgccgggcgtgg	Protospacer
.********.*** ************** .*

105. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022666 (Rhizobium leguminosarum bv. viciae strain BIHB 1217 plasmid pPR1, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
tgccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*********.*** *************  .  *.

106. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP016451 (Sinorhizobium sp. RAC02 plasmid pBSY16_2, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
aaccagatcaccggaaccgccgccgtcgccttcgc	Protospacer
 .**.********************.*** ..  *

107. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050086 (Rhizobium leguminosarum bv. trifolii strain 23B plasmid pRL23b7, complete sequence) position: , mismatch: 9, identity: 0.743

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
tgccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*********.*** *************  .  *.

108. spacer 8.11|2980267|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 10, identity: 0.706

tgaacgagctcgaagcggcggagggcatcggcga	CRISPR spacer
gcggtctggtcgaagcggcgcagcgcatcggcga	Protospacer
  ...  * *********** ** **********

109. spacer 8.11|2980267|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049358 (Deinococcus wulumuqiensis R12 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.706

tgaacgagctcgaagcggcggagggcatcggcga	CRISPR spacer
gcctctcgcccgaagcggcggcgggcatcggggc	Protospacer
    *  **.*********** ********* *

110. spacer 8.11|2980267|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP031159 (Deinococcus wulumuqiensis strain NEB 479 plasmid pDrdA, complete sequence) position: , mismatch: 10, identity: 0.706

tgaacgagctcgaagcggcggagggcatcggcga	CRISPR spacer
gcctctcgcccgaagcggcggcgggcatcggggc	Protospacer
    *  **.*********** ********* *

111. spacer 8.14|2980465|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_019898 (Thermobacillus composti KWC4 plasmid pTHECO01, complete sequence) position: , mismatch: 10, identity: 0.714

ggcggcttggcgaacagcaccgccatcgatccgca	CRISPR spacer
tatggcttggcgaacatcgccgccatcgtccttaa	Protospacer
 ..************* *.********* .*.  *

112. spacer 8.50|2982862|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to MK415399 (CrAssphage apr34_000142F, complete genome) position: , mismatch: 10, identity: 0.714

aacatcatcaccatcattaccatcacccatatata	CRISPR spacer
cgcatcatcactatcattaccattaccattaccat	Protospacer
 .*********.***********.***  **.

113. spacer 8.67|2983994|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP016619 (Microvirga ossetica strain V5/3m plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.706

ggggcacccagccgccgttcgtgccgagcagcga	CRISPR spacer
ccggcacccagccgccgtcggtgccggtgacctt	Protospacer
  ****************. ******.  * *

114. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048281 (Rhizobium leguminosarum bv. viciae 248 plasmid pRle248e, complete sequence) position: , mismatch: 10, identity: 0.706

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
cggcgatctcgatagccgcacccacggattcgag	Protospacer
. *********.***********.**. . * .*

115. spacer 8.82|2984985|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022568 (Rhizobium leguminosarum bv. viciae strain BIHB 1148 plasmid pSK04, complete sequence) position: , mismatch: 10, identity: 0.697

acacgaggccgtcggcggtgagccgtgggcggc	CRISPR spacer
tcacgaggccggcagcggtgagccgctagttct	Protospacer
 ********** *.***********. .*.  .

116. spacer 8.108|2986714|33|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP023000 (Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-B, complete sequence) position: , mismatch: 10, identity: 0.697

ctttgccccgcccggcttcaaggtcaacgcggt	CRISPR spacer
gaggacctcgcccggcttcaaggtcaacgatac	Protospacer
    .**.*********************  ..

117. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050104 (Rhizobium leguminosarum bv. trifolii strain 4B plasmid pRL4b2, complete sequence) position: , mismatch: 10, identity: 0.714

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
taccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*.*******.*** *************  .  *.

118. spacer 8.109|2986779|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP050109 (Rhizobium leguminosarum bv. trifolii strain 3B plasmid pRL3b2, complete sequence) position: , mismatch: 10, identity: 0.714

tgccggatcaccggaaccgccgccgccgcaccgtc	CRISPR spacer
taccggatcgccgtaaccgccgccgcccggaagcg	Protospacer
*.*******.*** *************  .  *.

119. spacer 8.7|2980001|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_014533 (Gloeothece verrucosa PCC 7822 plasmid Cy782201, complete sequence) position: , mismatch: 11, identity: 0.676

gtcgacgggtgtaggccgcggctttgtgggcgtg	CRISPR spacer
tattccgggtgaaggctgcggctttgtggttctc	Protospacer
  .  ****** ****.************ . *

120. spacer 8.14|2980465|35|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP029832 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed2, complete sequence) position: , mismatch: 11, identity: 0.686

ggcggcttggcgaacagcaccgccatcgatccgca	CRISPR spacer
atggagccggcgatcagcgccgccatcgatccgac	Protospacer
.  *. ..***** ****.**************

121. spacer 8.15|2980532|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012399 (Chelatococcus sp. CO-6 plasmid pCO-6, complete sequence) position: , mismatch: 11, identity: 0.676

cttcgagatcgccaaggagctcaagcaggaaaaa	CRISPR spacer
catcgagaccgccaaggaggtcaagctcttcggc	Protospacer
* ******.********** ******     ..

122. spacer 8.54|2983130|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 11, identity: 0.676

agagctcgaggcgatcgacatggaacagatgctc	CRISPR spacer
gcagatcgaggcgatcgacatgggacgccgcggc	Protospacer
. ** ******************.**.      *

123. spacer 8.54|2983130|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 11, identity: 0.676

agagctcgaggcgatcgacatggaacagatgctc	CRISPR spacer
gcagatcgaggcgatcgacatgggacgccgcggc	Protospacer
. ** ******************.**.      *

124. spacer 8.60|2983528|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP044989 (Deinococcus sp. AJ005 plasmid p380k, complete sequence) position: , mismatch: 11, identity: 0.676

aacaggtccgggatgaatacctactgggggatta	CRISPR spacer
gcccggtccgggatgaagacctgctgggtctgcg	Protospacer
. * ************* ****.*****    ..

125. spacer 8.72|2984322|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP040720 (Rhodococcus pyridinivorans strain YF3 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.676

ccaagcggcagatcaacaacgtggtgcgcgacgc	CRISPR spacer
cggtcacgcagatcaacgacctggtgcgcgatcg	Protospacer
* .    **********.** **********.

126. spacer 8.74|2984455|34|NZ_CP036280|CRISPRCasFinder,CRT,PILER-CR matches to NC_019849 (Sinorhizobium meliloti GR4 plasmid pRmeGR4d, complete sequence) position: , mismatch: 11, identity: 0.676

ttgcgatctcggtagccgcacccgcgaccgccgg	CRISPR spacer
gcggcgggtcgattgccgcacccgcgaccgcccc	Protospacer
 .*  .  ***.* ******************

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

282729 : 340301

Phage_21(14.29%)

transposase,integrase

attL 289002:289017|attR 346530:346545

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_145444504.1\|282729_283527_+\|transposase	transposase	NA	NA	NA	NA
WP_145444506.1\|283901_285146_-	NADP-dependent isocitrate dehydrogenase	Q77Z09	Phage_21	1.6e-18	81.5
WP_145444508.1\|285187_286234_-	NAD-dependent epimerase/dehydratase family protein	A0A2K9L4U8	Tupanvirus	2.2e-40	36.2
WP_145444511.1\|286482_288069_+	2-isopropylmalate synthase	E5EQ69	Micromonas_sp._RCC1109_virus	1.7e-07	24.3
WP_145444513.1\|288065_288653_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_145447190.1\|288738_290127_+	AAA family ATPase	A0A2I7SAD7	Vibrio_phage	3.7e-59	33.4
289002:289017	attL	NA	NA	NA	NA
WP_145444515.1\|290218_290944_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_145444517.1\|291014_291395_+	hypothetical protein	NA	NA	NA	NA
WP_145444519.1\|291478_291868_+	hypothetical protein	NA	NA	NA	NA
WP_145444521.1\|291951_292443_+	DNA starvation/stationary phase protection protein Dps	NA	NA	NA	NA
WP_145444523.1\|292471_295471_+	alpha-mannosidase	NA	NA	NA	NA
WP_145444524.1\|295546_295714_-	hypothetical protein	NA	NA	NA	NA
WP_145444526.1\|295741_297076_-	hypothetical protein	NA	NA	NA	NA
WP_145444528.1\|297251_297671_+	transcriptional repressor	NA	NA	NA	NA
WP_145444530.1\|297839_299534_+	PEP-CTERM sorting domain-containing protein	NA	NA	NA	NA
WP_145444532.1\|299734_300283_+	hypothetical protein	NA	NA	NA	NA
WP_145444534.1\|300343_301828_-	response regulator	Q8QKV7	Ectocarpus_siliculosus_virus	6.5e-38	30.5
WP_145444536.1\|301824_302958_-	histidine kinase	NA	NA	NA	NA
WP_145444538.1\|303222_304140_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_145444540.1\|304261_305689_-	hypothetical protein	NA	NA	NA	NA
WP_145444542.1\|305420_306941_-	hypothetical protein	NA	NA	NA	NA
WP_145444544.1\|306844_307117_-	hypothetical protein	NA	NA	NA	NA
WP_145444546.1\|307116_307896_-	hypothetical protein	NA	NA	NA	NA
WP_145444548.1\|307892_308321_-	hypothetical protein	NA	NA	NA	NA
WP_145444550.1\|308359_308596_-	hypothetical protein	NA	NA	NA	NA
WP_145444552.1\|308767_309391_-	hypothetical protein	NA	NA	NA	NA
WP_145444554.1\|309387_310401_-	protein rep	NA	NA	NA	NA
WP_145444556.1\|310634_310895_-	hypothetical protein	NA	NA	NA	NA
WP_145444558.1\|310899_311172_-	hypothetical protein	NA	NA	NA	NA
WP_145444560.1\|311606_312887_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_145444562.1\|312937_313351_+	hypothetical protein	NA	NA	NA	NA
WP_145444564.1\|313347_313890_+	hypothetical protein	NA	NA	NA	NA
WP_145444566.1\|314542_315475_+	NmrA family NAD(P)-binding protein	NA	NA	NA	NA
WP_145444567.1\|315487_316825_+	MFS transporter	NA	NA	NA	NA
WP_145444569.1\|317628_318195_+\|transposase	IS3 family transposase	S5WIU1	Leptospira_phage	5.7e-19	37.2
WP_145444571.1\|318250_319297_+\|transposase	IS110 family transposase	NA	NA	NA	NA
WP_145444573.1\|319903_320824_-	N-acetylglucosamine-6-phosphate deacetylase	NA	NA	NA	NA
WP_145444575.1\|320820_321573_-	glucosamine-6-phosphate deaminase	NA	NA	NA	NA
WP_145444577.1\|321609_323655_-	sodium:solute symporter	NA	NA	NA	NA
WP_145444579.1\|323651_325085_-	family 20 glycosylhydrolase	NA	NA	NA	NA
WP_145444580.1\|325171_326110_-	hypothetical protein	NA	NA	NA	NA
WP_145444582.1\|326419_327562_+	ROK family protein	NA	NA	NA	NA
WP_145444585.1\|327571_329116_+	family 20 glycosylhydrolase	A0A2H4UUW7	Bodo_saltans_virus	1.6e-10	29.2
WP_145444587.1\|330185_331328_+	ROK family protein	NA	NA	NA	NA
WP_145444589.1\|331348_334078_+	hypothetical protein	NA	NA	NA	NA
WP_145444592.1\|334243_334855_+	PEP-CTERM sorting domain-containing protein	NA	NA	NA	NA
WP_145444594.1\|334733_336089_+	PEP-CTERM sorting domain-containing protein	NA	NA	NA	NA
WP_145444596.1\|336121_338140_+	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_145444598.1\|338136_339219_+	family 16 glycosylhydrolase	NA	NA	NA	NA
WP_145444600.1\|339821_340301_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
346530:346545	attR	NA	NA	NA	NA

DBSCAN-SWA_2

1140399 : 1149086

Vibrio_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_145445196.1\|1140399_1141551_+	Fic family protein	D7RWK9	Brochothrix_phage	6.8e-35	31.4
WP_145445197.1\|1141556_1142969_-	ParB N-terminal domain-containing protein	A0A2H4JGF1	uncultured_Caudovirales_phage	1.5e-76	41.2
WP_145445198.1\|1143292_1145845_-	DUF3987 domain-containing protein	A0A088FAP0	Vibrio_phage	5.8e-18	23.6
WP_145445199.1\|1145941_1146181_+	AbrB/MazE/SpoVT family DNA-binding domain-containing protein	NA	NA	NA	NA
WP_145445200.1\|1146171_1146498_+	type II toxin-antitoxin system PemK/MazF family toxin	NA	NA	NA	NA
WP_145445201.1\|1146509_1148216_-	DEAD/DEAH box helicase family protein	A0A172PZU9	Pseudomonas_phage	4.6e-96	36.1
WP_145445202.1\|1148215_1148602_-	RusA family crossover junction endodeoxyribonuclease	K7PKN5	Enterobacterial_phage	6.7e-19	40.9
WP_145445203.1\|1148612_1149086_-	DUF669 domain-containing protein	A0A088FAP5	Vibrio_phage	2.1e-27	50.4

DBSCAN-SWA_3

1266648 : 1278081

uncultured_virus(50.0%)

tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_145447224.1\|1266648_1267884_-\|tRNA	tyrosine--tRNA ligase	K4F5T3	Cronobacter_phage	1.4e-73	38.8
WP_145445304.1\|1267925_1268270_-	zinc ribbon domain-containing protein	NA	NA	NA	NA
WP_145445305.1\|1268303_1268879_-	nucleotide exchange factor GrpE	NA	NA	NA	NA
WP_145445306.1\|1268894_1270031_-	molecular chaperone DnaJ	A0A1V0SBY2	Catovirus	9.4e-29	28.6
WP_145445307.1\|1270115_1271729_-	chaperonin GroEL	A0A240F779	uncultured_virus	5.8e-149	53.6
WP_145445308.1\|1271811_1272132_-	co-chaperone GroES	A0A221S308	uncultured_virus	2.8e-15	45.7
WP_145445309.1\|1272194_1273901_-	chaperonin GroEL	A0A219YK78	uncultured_virus	5.4e-153	55.0
WP_145445310.1\|1274169_1278081_-	ATP-dependent RNA helicase HrpA	A0A2K9L482	Tupanvirus	3.4e-46	28.6

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_CP036280

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection