CRISPRimmunity

Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP042437	Mucilaginibacter ginsenosidivorax strain KHI28 chromosome, complete genome	14 crisprs	RT,DEDDh,csa3,PD-DExK,cas3,WYL,cas2,cas1,cas9	1	55	1	0

1. NZ_CP042437

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP042437_1

• CRISPR_ID: NZ_CP042437_1
• CRISPR_location: 1182229-1182334
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_1

Consensus_repeat	Method
CTCACACCTCCCAAAACAGACAACA	CRISPRCasFinder

spacers of NZ_CP042437_1

>1.1|1182254|56|NZ_CP042437|CRISPRCasFinder
TCGTGGATCTTTGTTATTTTTAATTTAATATTTAACCTTGTATTTAAGTATCAGAC

CRISPR arrays and Neighbor proteins around NZ_CP042437_1

CRISPR arrays

The CRISPR arrays of NZ_CP042437_1

>merge|NZ_CP042437|1|1182229-1182334|CRISPRCasFinder
CTCACACCTCCCAAAACAGACAACATCGTGGATCTTTGTTATTTTTAATTTAATATTTAACCTTGTATTTAAGTATCAGACCTCACACCTCCCAAAACAGACAACA

>NZ_CP042437|1|1|1182229-1182334|CRISPRCasFinder
CTCACACCTCCCAAAACAGACAACA	TCGTGGATCTTTGTTATTTTTAATTTAATATTTAACCTTGTATTTAAGTATCAGAC
CTCACACCTCCCAAAACAGACAACA

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147052426.1|1180823_1182137_+|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|224172
NZ_CP042437.1|WP_147052418.1|1171491_1172718_+|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl|CDD|223745
NZ_CP042437.1|WP_147052424.1|1176973_1177456_+|dihydrofolate-reductase	unknown	unknown	gnl|CDD|365932
NZ_CP042437.1|WP_147052423.1|1176593_1176977_+|type-II-toxin-antitoxin-system-death-on-curing-family-toxin	unknown	unknown	gnl|CDD|226180
NZ_CP042437.1|WP_147052427.1|1182335_1183187_+|hydroxymethylglutaryl-CoA-lyase	unknown	unknown	gnl|CDD|163676
NZ_CP042437.1|WP_147052421.1|1175461_1176283_+|thymidylate-synthase	unknown	unknown	gnl|CDD|234984
NZ_CP042437.1|WP_147052431.1|1185791_1186304_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052422.1|1176408_1176597_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052434.1|1187454_1187829_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052429.1|1184668_1185112_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052417.1|1170353_1171376_+|Holliday-junction-branch-migration-DNA-helicase-RuvB	unknown	unknown	gnl|CDD|234619
NZ_CP042437.1|WP_147052420.1|1174225_1175026_-|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase	unknown	unknown	gnl|CDD|237766
NZ_CP042437.1|WP_147052432.1|1186323_1187016_-|DUF4288-domain-containing-protein	unknown	unknown	gnl|CDD|379479
NZ_CP042437.1|WP_147052435.1|1187831_1188554_-|hypothetical-protein	unknown	unknown	gnl|CDD|378271
NZ_CP042437.1|WP_147052430.1|1185163_1185694_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052433.1|1187012_1187444_-|hypothetical-protein	unknown	unknown	gnl|CDD|319943
NZ_CP042437.1|WP_147052428.1|1183289_1184516_-|ROK-family-protein	unknown	unknown	gnl|CDD|224851
NZ_CP042437.1|WP_147052425.1|1177572_1180560_+|protein-translocase-subunit-SecDF	unknown	unknown	gnl|CDD|237276
NZ_CP042437.1|WP_147052436.1|1188572_1189016_-|DUF695-domain-containing-protein	unknown	unknown	gnl|CDD|368292
NZ_CP042437.1|WP_147052419.1|1173222_1174101_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147052426.1|1180823_1182137_+|FAD-dependent-oxidoreductase	gnl|CDD|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	7.46052e-125
NZ_CP042437.1|WP_147052418.1|1171491_1172718_+|Gfo/Idh/MocA-family-oxidoreductase	gnl|CDD|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	1.02848e-28
NZ_CP042437.1|WP_147052424.1|1176973_1177456_+|dihydrofolate-reductase	gnl|CDD|365932	pfam00186, DHFR_1, Dihydrofolate reductase.	1.25383e-89
NZ_CP042437.1|WP_147052423.1|1176593_1176977_+|type-II-toxin-antitoxin-system-death-on-curing-family-toxin	gnl|CDD|226180	COG3654, Doc, Prophage maintenance system killer protein [General function prediction only].	7.05915e-21
NZ_CP042437.1|WP_147052427.1|1182335_1183187_+|hydroxymethylglutaryl-CoA-lyase	gnl|CDD|163676	cd07938, DRE_TIM_HMGL, 3-hydroxy-3-methylglutaryl-CoA lyase, catalytic TIM barrel domain. 3-hydroxy-3-methylglutaryl-CoA lyase (HMGL) catalyzes the cleavage of HMG-CoA to acetyl-CoA and acetoacetate, one of the terminal steps in ketone body generation and leucine degradation, and is a key enzyme in the pathway that supplies metabolic fuel to extrahepatic tissues. Mutations in HMGL cause a human autosomal recessive disorder called primary metabolic aciduria that affects ketogenesis and leucine catabolism and can be fatal due to an inability to tolerate hypoglycemia. HMGL has a TIM barrel domain with a catalytic center containing a divalent cation-binding site formed by a cluster of invariant residues that cap the core of the barrel. The cleavage of HMG-CoA requires the presence of a divalent cation like Mg2+ or Mn2+, and the reaction is thought to involve general acid/base catalysis. This family belongs to the DRE-TIM metallolyase superfamily. DRE-TIM metallolyases include 2-isopropylmalate synthase (IPMS), alpha-isopropylmalate synthase (LeuA), 3-hydroxy-3-methylglutaryl-CoA lyase, homocitrate synthase, citramalate synthase, 4-hydroxy-2-oxovalerate aldolase, re-citrate synthase, transcarboxylase 5S, pyruvate carboxylase, AksA, and FrbC. These members all share a conserved triose-phosphate isomerase (TIM) barrel domain consisting of a core beta(8)-alpha(8) motif with the eight parallel beta strands forming an enclosed barrel surrounded by eight alpha helices. The domain has a catalytic center containing a divalent cation-binding site formed by a cluster of invariant residues that cap the core of the barrel. In addition, the catalytic site includes three invariant residues - an aspartate (D), an arginine (R), and a glutamate (E) - which is the basis for the domain name "DRE-TIM".	2.71823e-103
NZ_CP042437.1|WP_147052421.1|1175461_1176283_+|thymidylate-synthase	gnl|CDD|234984	PRK01827, thyA, thymidylate synthase; Reviewed.	0
NZ_CP042437.1|WP_147052435.1|1187831_1188554_-|hypothetical-protein	gnl|CDD|378271	pfam09844, DUF2071, Uncharacterized conserved protein (COG2071). This conserved protein (similar to YgjF), found in various prokaryotes, has no known function.	2.07836e-06
NZ_CP042437.1|WP_147052433.1|1187012_1187444_-|hypothetical-protein	gnl|CDD|319943	cd08355, TioX_like, Micromonospora sp. TioX and similar proteins. Micromonospora sp. TioX is encoded by a gene of the thiocoraline biosynthetic gene cluster. Thiocoraline is a thiodepsipeptide with potent antitumor activity. TioX may be involved in thiocoraline resistance or secretion. TioX belongs to vicinal oxygen chelate (VOC) superfamily that is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	6.02685e-23
NZ_CP042437.1|WP_147052417.1|1170353_1171376_+|Holliday-junction-branch-migration-DNA-helicase-RuvB	gnl|CDD|234619	PRK00080, ruvB, Holliday junction branch migration DNA helicase RuvB.	0
NZ_CP042437.1|WP_147052420.1|1174225_1175026_-|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase	gnl|CDD|237766	PRK14609, PRK14609, 4-diphosphocytidyl-2-C-methyl-D-erythritol kinase; Provisional.	2.16379e-148
NZ_CP042437.1|WP_147052432.1|1186323_1187016_-|DUF4288-domain-containing-protein	gnl|CDD|379479	pfam14119, DUF4288, Domain of unknown function (DUF4288). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 120 amino acids in length.	1.62668e-13
NZ_CP042437.1|WP_147052428.1|1183289_1184516_-|ROK-family-protein	gnl|CDD|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	4.35708e-46
NZ_CP042437.1|WP_147052425.1|1177572_1180560_+|protein-translocase-subunit-SecDF	gnl|CDD|237276	PRK13024, PRK13024, bifunctional preprotein translocase subunit SecD/SecF; Reviewed.	0
NZ_CP042437.1|WP_147052436.1|1188572_1189016_-|DUF695-domain-containing-protein	gnl|CDD|368292	pfam05117, DUF695, Family of unknown function (DUF695). Family of uncharacterized bacterial proteins.	2.8541e-16

Protein sequences

>NZ_CP042437.1|WP_147052426.1|1180823_1182137_+|FAD-dependent-oxidoreductase
MNTSDSSKFPLVVIVGGGFGGLQVAKKLADKPVDVLMLDKHNYHTFQPLLYQVAMGGLESESIAFSLRKNFSGQKNFRFRIAEVLKVDAANNTIDTTIGPIAYDYLVIATGSTTNFFGNHDIEKFSMPMKSIPEALNLRYSVLQNIEEALLKTSKDEREALLTFVLVGAGPTGVELSGSLAELRNHVLTKDYPELKKEDMKVYLVDFLPKVLGPFSDQASNAAKDFLTKMGVEVLLGVKVESYDGKEIKFEGGKTIRTKNVIWSAGVMGVVPEGIEKGNIERGNRIKVDNICRMVGTENIFAIGDVAAMITDETPKGHPGVAQVAIQMGAHVGKTIMQLINHEPTTPFKYFDKGSLATIGRNKAVADLGKIRFQGFFAWLVWMFVHLISLLGGRNKVIVFINWVSSYINYNGGTRLIIRKFEREGLTEDEHLPKTVD
>NZ_CP042437.1|WP_147052425.1|1177572_1180560_+|protein-translocase-subunit-SecDF
MQGKGVIKFFAILLAVVCIYQLSFTWVAQKVESDAKAYAKGNAEKEKAYLDSMSTQPVYPIFKHTYAFVLQRELALGLDLKGGMNVTMQIQLDELVRKIANDNPDATFNQALANADKLQANAKTSQKDYIALFVSEYEKLNPDGKLAAIFSTKDNQDHLKFNATNSEVEAYLRDLASTAVKQSFTVLNTRINQFGVTQPNIQLEASSNRILIELPGVKEPDRVRKLLSGTAKLEFYQTFDNSEAYQTIIAIDNLLGAKNKTIAKTDTTKTTATAAAKTDTAKKAGSLLSKVQKSAEKDTSASALAGKSQLAAQHPLLSVMSLNLYPGQNGQQQLGSGPVVGYALLKDTAKVNSYLHSKLAQSAIPRNMKFLWDVKPMKDAKQKAFALYAIKLSGAENGPVLSGSVITDARADVNQKGSPEVVMIMNSEGAQKWRAVTAEAAAATNKRAIAIVLDDNVYSAPNVQNEISGGVSSIEGSFTQEDTRDLANVLKAGRLPAPAHIVSEDVVGPSLGKQAIAASLLSCVLGLVVVLVFMIAYYNRAGTVAVVAVIINIFFLMGVLTSLGAVLTVPGVAGIVLTLGIAVDANVLVYERVREELALGKSLKIAVADGFKHALPSILDSQISTFLTGLILFIFGSGPIQGFATTLMIGIITSLFCSLLISRVIFEWMLEKGWDIKFSNPWSSHTFKNANYAFVKNRFKFYIFSGTFIIAGIISIFVRGFSYGVDFEGGRNFIITFPNKNITTEQIHSVVDPSLLGRGTEVKTVNADKISITTNYLIQQNTPAVDVQVRKTLIEALATKPETKISDSDIQGQSKVSATIAEELKTSAVYTVLIAILVISAYIFIRFRKWQFSLGAMVATAHDALLVLSFFSLFNGILPFSLDIDQAFIAAILTVIGYSINDTVVVFDRIREFLDHKSKDEQTEDVINRAINSTLSRTIITALTVIFVLIVLFIFGGDVIKGFSFALLIGVIFGTYSSICVATPVIVDFGKKDLK
>NZ_CP042437.1|WP_147052424.1|1176973_1177456_+|dihydrofolate-reductase
MIVSIIVAIAKNHAIGKDNKLLWYLPNDLKHFKDVTSGHTVIMGRKTFDSVGKPLPRRRNIVITRQDISIEGCEVVKSIEAALVLCAAEDEIFIVGGAEIYRQAIPLTNRIYLTIIDQEFEGDTFFPELNTGDWQETQRENFEPDDKNKYSYSFITLERR
>NZ_CP042437.1|WP_147052423.1|1176593_1176977_+|type-II-toxin-antitoxin-system-death-on-curing-family-toxin
MISIQSVLYIHSQLIKNFGGGEGVRDQGGLEAAIARPYATFDGIDLYPEPIDKAAAIFESLIINHPFIDGNKRTAYTLLRLMLLGFGWDIEASEDEKYDMTIAASTGKLKFDEIKLWLSEKTITKNK
>NZ_CP042437.1|WP_147052422.1|1176408_1176597_+|hypothetical-protein
MTAVQIKEEIQKALNDMPETALADVLNFVKQFQTHPFDQSTLDNNLKKIMSEDKGLLERLAK
>NZ_CP042437.1|WP_147052421.1|1175461_1176283_+|thymidylate-synthase
MKQYLDLMKHVLETGAQKHDRTGTGTVSVFGYQMRFNLKDGFPMVTTKKLHLKSIIHELIWFLSGDSNIRYLKENGVRIWDEWADADGNLGPVYGVQWRSWPTPDGGHIDQIAQVVNQIKNNPDSRRMIVSAWNVAEVNQMALPPCHSLFQFYVEPANPLKGESKGKLSCQLYQRSADIFLGVPFNIASYALLTMMMAQVCDLDYGDFIHTLGDAHLYNNHLEQVNLQLSREPRPLPTMKINPEVKDIFGFKFEDFTLENYDPHPHIKGVVAV
>NZ_CP042437.1|WP_147052420.1|1174225_1175026_-|4-(cytidine-5'-diphospho)-2-C-methyl-D-erythritol-kinase
MILFPNAKINIGLNITERRPDGYHNLETIFYPVNIKDALEVVESDELTFTSSGLDIPGRAEDNLCVKGYHMLKKDFDIPPVSIHLHKNIPIGAGLGGGSADAAFFIRLMNEQFNLCISVDEMTGYARRLGADCAFFIENKPVFAFERGDEFETIKLDLSAYKIVLVMPDIHISTSEAFSGIKPTPVKDSLLELITEPITEWKKHIKNDFETSIFKNHIEIRGVKAALYEAGAIYASMSGSGASVFGIFDHTPDLGFLETDNEVFYL
>NZ_CP042437.1|WP_147052419.1|1173222_1174101_+|hypothetical-protein
MKRSVLLFLAALALLGCGSKKKKVAATVYPTISYLNIKLDAVGHLPSNPYILTFDNAEKHIVFCGVNHVDKNKINDPMYAGIEKAFFAFKPDVCVNEGGDVSKKVFASKQAALRKDGEIGLVKILADSLKIKTVNGDMTDSLEFKELLKKYTPGEFLAYIVTERFMWGLNEQQANDTVNLKKSYAGFIQNYIMKTGAVKLTPQQQTLAFYKTNYQKLLKRPFIFNELEPTNPFDPKGKFQEIGRASKEIRDQSLLATIDSLLKTHNKVFVVFGGWHLLTCEPGLKQIISRAK
>NZ_CP042437.1|WP_147052418.1|1171491_1172718_+|Gfo/Idh/MocA-family-oxidoreductase
MKTMFNHGVKFFFTMLFVSCAAITMAQTTIPAPTTPMVPNKPEALPADTAKKLGKDTALTKKDTIPVKKIPTGPKVGIAGLNHDHIHLILNEYRNGNVNIVGIAEPDKKLWAKYGKMYGVPDSLFFEDLKTMCLARKPVIVLGYNAVGKHIDVVETCAPLHISVMVEKPLAATLEQARRMEFLALKYYISLLTNYETTWYPSVQSAYNTVKTDSVGIIRKMVFHDGHQGPREIGCSEDFLSWLTDPILNGAGALNDFGCYGANMMTWLMQGQRPIAVTAVARHYKPSVYPKVEDDATIIVEYPNATGMIEASWNWPYGIKDMEIFGAKGYIHTFDKDSVEVRVNNSVHSFKAPALPAPADAPVPYFTAALKNPIKSHNDRSSLRYNMIVMQILDAAKRSIKEGKRIVL
>NZ_CP042437.1|WP_147052417.1|1170353_1171376_+|Holliday-junction-branch-migration-DNA-helicase-RuvB
MNEHLDPAPERLSNTERDIEKVLRPQQFEDFTGQHKILANLKIFVQAARQRGEALDHVLLHGPPGLGKTTLSHIIANEMSVGIKITSGPVLDKPGDLAGLLTNLETGDILFIDEIHRLSPLVEEYLYSAMEDFKIDIMLESGPNARSVQISLNPFTLVGATTRSGLLTAPLRARFGINARLEYYDAKLLTTIVLRSSSILKTPITDEGAYEIARRSRGTPRIANALLRRTRDFAQIKGDGNIDTAIAKYALNALNVDEHGLDEMDNKILSTIIDKFKGGPVGLKTIATAVGEDEGTIEEVYEPFLIQEGFLMRTARGRECTESAYKHLGKIKLGGNPSLF
>NZ_CP042437.1|WP_147052427.1|1182335_1183187_+|hydroxymethylglutaryl-CoA-lyase
MPIKITECPRDAMQGIVHFIPTDIKAAYINLLLQVGFDTIDFGSFVSAKAIPQLQDTAEVLSKLDLSNTQSKLLAIIANYRGAEEAVKHPEITYLGYPFSISETFQLRNTNTTLSQAFENVKRMQELAIANNKKLLVYLSMGFGNPYGDEWNTGVIHDWTGKLVKQGIDNIALADTIGISEPDQISSIYPELCLAFPKTEFGIHLHSTPDTWQPKIEAAYQSGCKRFDTAIKGYGGCPMAADDLTGNIATENLIVYLESQKEPTGLYMDKFREAMEYSGRVFL
>NZ_CP042437.1|WP_147052428.1|1183289_1184516_-|ROK-family-protein
MEPENKGVKGSQLKNMIIKRLYFNKAMSCAGLSDLFDKSIPSIAKAINELMHEGFVVEHGYAPSSGGRRPLMYSVKANAMYILAVALDQLTARIQLFDLQNSPVADMLTFELKLLNNPNALTILTNQINSYIKTSGVAKGKIAGIGIGMPGFINVTQGINYTYLDANGSLTAYLTEHTGITTYIDNDSSLIALAEQKFGIAKAQTEVMVINLGWGIGLGMIVNGKLFRGHNGFAGELSHIPLSEDGSLCECGKRGCLEAEASMLVVARKAIEGIQQGRITSLKHNTNDHSKLMGDALLDAANNGDQFAIELLSDAGYKIGKALAILIHIMNPAIIVLSGRGAKVAKILMAPIQQALHKYCIPRLSAGTELLVSELGFDAELVGAAVLVMENFDKTVKAKVAKAAKTIV
>NZ_CP042437.1|WP_147052429.1|1184668_1185112_-|hypothetical-protein
MRFKPHFEKIRFIFGAIVVVTISGCFQIFGSGPATFIKKSFNPSKTKQAILFWKGGNATSGNSLQVSIKGAGDDLDKAEVGNVFTVDDDHGKARLNPKAIRLIWKSDRQLNIEYDVNLRTFIQLKRFNDDTIVYRTFKPVIPANHMD
>NZ_CP042437.1|WP_147052430.1|1185163_1185694_-|hypothetical-protein
MAAMGHFIFELFKIAILSFIYSVLLGILHLIFLTAKGIEPVFDKRTFNRLFKIVYASLFVFSFTYYGNHGLGDEYNIPLGYGETMQAGDLLPCFYPKGKNQVAVKNYLVRGDKLCATIDSGVMVYNLNTKRLKDFNSDEQYNAYAEDHDLPPTNQFLGFEQQYHDYWSGWRFWVLP
>NZ_CP042437.1|WP_147052431.1|1185791_1186304_-|hypothetical-protein
MPAFTKIIAICLLTLSACSSSPRKNPAKNQHKKVLAAHEYINTRLSGTGKIPREVFIVDSTAAVFTILDTTEIQKRHKASTDEEFYAGADDQVFYTSEARTFLKKQPVKIIELDPAYKYLEFKQANGVVHRIKLDTVAFISNLYFFNPQKQSHNVDMLDVEAEYKKYFGK
>NZ_CP042437.1|WP_147052432.1|1186323_1187016_-|DUF4288-domain-containing-protein
MKEIYDLEYWQLDKSVSNTKRFAIVKINLVYPKVKQLTDLKPKERVKKIDSIYREDLTRLIALNLFDTYEITGKKKRPTGVTAKVKFNDLKKLKKVDFVASIWVTSVDHAIFIKAEEPPKEQYYCVKMTGVIEVEGVRLKKQDIEKRFVLIKAWSFNDAYDKVKKQQENYCEPYLNPNGRFVRWRIESYDDCFVTDIGNPAELDNPEGVEVFSALGKRKNKLKTVWDGKP
>NZ_CP042437.1|WP_147052433.1|1187012_1187444_-|hypothetical-protein
MGTSNQQIIPMLAYEDGIAAMEWLCKVFGFTEVTRMTDEQGRLGHGEIAMGESLVMLAEPTPDYQGPKHHAQNCTIAAKAYEVPYVINGVLVYVDDVTLHYEHAKSNGATILSVLEEGYPGTRYRAADLEGQRWMFMQKEILK
>NZ_CP042437.1|WP_147052434.1|1187454_1187829_-|hypothetical-protein
MPISIFRKIKFDALVIITSLLISGTYILDRVVLFFLRIYLRNHYDSHFLTKNKEQADIKGIAYWSLFIESYYLIVFHLLVLTAVLLVFFHKQLRLYKRELLWAYLIIVVCDIGYFVVARLFVKH
>NZ_CP042437.1|WP_147052435.1|1187831_1188554_-|hypothetical-protein
MKIPTITGIIDRRILVNFAVDPDIAKLIVPAPFSPKIVNGKAIVGICLIRLKDVRPKGMPAFIGMGSENGAHRIAVEWQEDGEIKEGVYIPRRDTSSRFNTIVGGRIFPGRHYHARFDVNEHSGNYHVAFESSDGTTISIDAKITGTFNRDSVFKDLDTASDFFKAGATGYSPNGDKYEGLLLHTENWKVEALEVSQVSSSFFEDEAIFPKGTIVFDNALLMTNIQHDWYSKPDKAVVND
>NZ_CP042437.1|WP_147052436.1|1188572_1189016_-|DUF695-domain-containing-protein
MIEELYLGDSWISLEFSTDGGLPVFVKFRPYMQNFIDTGFYNQRMDVIWSYNSPNETLLPHETDLDLMEQVEEALMDVMEEDNQTILAFSFTGENERWWAWYTTDVDIAGERLNAALAGFEELPISITANTDPDWDEYNGVLEDFAE

Crispr_ID: NZ_CP042437_2

• CRISPR_ID: NZ_CP042437_2
• CRISPR_location: 1755502-1755591
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_2

Consensus_repeat	Method
TCACCGATTAAGAATGATTTCACCGATTTT	CRISPRCasFinder

spacers of NZ_CP042437_2

>2.1|1755532|30|NZ_CP042437|CRISPRCasFinder
ATTGTTAAAGTTTATATTAAAGTTGGGATT

CRISPR arrays and Neighbor proteins around NZ_CP042437_2

CRISPR arrays

The CRISPR arrays of NZ_CP042437_2

>merge|NZ_CP042437|2|1755502-1755591|CRISPRCasFinder
TCACCGATTAAGAATGATTTCACCGATTTTATTGTTAAAGTTTATATTAAAGTTGGGATTTCACCGATTAAGGATGATTTCACCGATTTT

>NZ_CP042437|2|2|1755502-1755591|CRISPRCasFinder
TCACCGATTAAGAATGATTTCACCGATTTT	ATTGTTAAAGTTTATATTAAAGTTGGGATT
TCACCGATTAAGGATGATTTCACCGATTTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147060908.1|1758272_1759955_-|dihydroxy-acid-dehydratase	unknown	unknown	gnl|CDD|234861
NZ_CP042437.1|WP_147052970.1|1754420_1755479_-|ketol-acid-reductoisomerase	unknown	unknown	gnl|CDD|273093
NZ_CP042437.1|WP_147052965.1|1748657_1749413_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|226591
NZ_CP042437.1|WP_147052964.1|1747384_1748551_-|2-isopropylmalate-synthase	unknown	unknown	gnl|CDD|234864
NZ_CP042437.1|WP_147052967.1|1750683_1751478_-|methyltransferase-domain-containing-protein	unknown	unknown	gnl|CDD|181382
NZ_CP042437.1|WP_147052974.1|1763964_1764963_-|zinc-binding-dehydrogenase	unknown	unknown	gnl|CDD|176180
NZ_CP042437.1|WP_147052963.1|1746131_1747382_-|threonine-ammonia-lyase-IlvA	unknown	unknown	gnl|CDD|236318
NZ_CP042437.1|WP_147052969.1|1752849_1754262_-|3-isopropylmalate-dehydratase-large-subunit	unknown	unknown	gnl|CDD|235490
NZ_CP042437.1|WP_090643183.1|1760851_1762357_-|F0F1-ATP-synthase-subunit-beta	unknown	unknown	gnl|CDD|236447
NZ_CP042437.1|WP_147052975.1|1765039_1765252_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052966.1|1749538_1750630_-|3-isopropylmalate-dehydrogenase	unknown	unknown	gnl|CDD|234832
NZ_CP042437.1|WP_090643187.1|1760511_1760766_-|ATP-synthase-F1-subunit-epsilon	unknown	unknown	gnl|CDD|213395
NZ_CP042437.1|WP_147052962.1|1745742_1746135_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052976.1|1767053_1767992_-|DNRLRE-domain-containing-protein	unknown	unknown	gnl|CDD|366248
NZ_CP042437.1|WP_147060909.1|1765420_1767016_+|hydroxymethylbilane-synthase	unknown	unknown	gnl|CDD|234612
NZ_CP042437.1|WP_147052972.1|1756423_1758163_-|biosynthetic-type-acetolactate-synthase-large-subunit	unknown	unknown	gnl|CDD|272915
NZ_CP042437.1|WP_147052971.1|1755779_1756382_-|acetolactate-synthase-small-subunit	unknown	unknown	gnl|CDD|183365
NZ_CP042437.1|WP_147052968.1|1751587_1752178_-|3-isopropylmalate-dehydratase-small-subunit	unknown	unknown	gnl|CDD|179314
NZ_CP042437.1|WP_147052973.1|1762633_1763980_+|G-D-S-L-family-lipolytic-protein	unknown	unknown	gnl|CDD|238863
NZ_CP042437.1|WP_147052961.1|1744074_1745736_-|hypothetical-protein	unknown	unknown	gnl|CDD|223619

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147060908.1|1758272_1759955_-|dihydroxy-acid-dehydratase	gnl|CDD|234861	PRK00911, PRK00911, dihydroxy-acid dehydratase; Provisional.	0
NZ_CP042437.1|WP_147052970.1|1754420_1755479_-|ketol-acid-reductoisomerase	gnl|CDD|273093	TIGR00465, Ketol-acid_reductoisomerase, ketol-acid reductoisomerase. This is the second enzyme in the parallel isoleucine-valine biosynthetic pathway [Amino acid biosynthesis, Pyruvate family].	1.79588e-108
NZ_CP042437.1|WP_147052965.1|1748657_1749413_-|methyltransferase-domain-containing-protein	gnl|CDD|226591	COG4106, Tam, Trans-aconitate methyltransferase [General function prediction only].	2.20701e-31
NZ_CP042437.1|WP_147052964.1|1747384_1748551_-|2-isopropylmalate-synthase	gnl|CDD|234864	PRK00915, PRK00915, 2-isopropylmalate synthase; Validated.	0
NZ_CP042437.1|WP_147052967.1|1750683_1751478_-|methyltransferase-domain-containing-protein	gnl|CDD|181382	PRK08317, PRK08317, hypothetical protein; Provisional.	4.81902e-27
NZ_CP042437.1|WP_147052974.1|1763964_1764963_-|zinc-binding-dehydrogenase	gnl|CDD|176180	cd05276, p53_inducible_oxidoreductase, PIG3 p53-inducible quinone oxidoreductase. PIG3 p53-inducible quinone oxidoreductase, a medium chain dehydrogenase/reductase family member, acts in the apoptotic pathway. PIG3 reduces ortho-quinones, but its apoptotic activity has been attributed to oxidative stress generation, since overexpression of PIG3 accumulates reactive oxygen species. PIG3 resembles the MDR family member quinone reductases, which catalyze the reduction of quinone to hydroxyquinone. NAD(P)(H)-dependent oxidoreductases are the major enzymes in the interconversion of alcohols and aldehydes or ketones. Alcohol dehydrogenase in the liver converts ethanol and NAD+ to acetaldehyde and NADH, while in yeast and some other microorganisms ADH catalyzes the conversion acetaldehyde to ethanol in alcoholic fermentation. ADH is a member of the medium chain alcohol dehydrogenase family (MDR), which has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The NAD(H)-binding region is comprised of 2 structurally similar halves, each of which contacts a mononucleotide. A GxGxxG motif after the first mononucleotide contact half allows the close contact of the coenzyme with the ADH backbone. The N-terminal catalytic domain has a distant homology to GroES. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit, a catalytic zinc at the active site, and a structural zinc in a lobe of the catalytic domain. NAD(H) binding occurs in the cleft between the catalytic and coenzyme-binding domains at the active site, and coenzyme binding induces a conformational closing of this cleft. Coenzyme binding typically precedes and contributes to substrate binding. In human ADH catalysis, the zinc ion helps coordinate the alcohol, followed by deprotonation of a histidine, the ribose of NAD, a serine, then the alcohol, which allows the transfer of a hydride to NAD+, creating NADH and a zinc-bound aldehyde or ketone. In yeast and some bacteria, the active site zinc binds an aldehyde, polarizing it, and leading to the reverse reaction.	0
NZ_CP042437.1|WP_147052963.1|1746131_1747382_-|threonine-ammonia-lyase-IlvA	gnl|CDD|236318	PRK08639, PRK08639, threonine dehydratase; Validated.	0
NZ_CP042437.1|WP_147052969.1|1752849_1754262_-|3-isopropylmalate-dehydratase-large-subunit	gnl|CDD|235490	PRK05478, PRK05478, 3-isopropylmalate dehydratase large subunit.	0
NZ_CP042437.1|WP_147052966.1|1749538_1750630_-|3-isopropylmalate-dehydrogenase	gnl|CDD|234832	PRK00772, PRK00772, 3-isopropylmalate dehydrogenase; Provisional.	0
NZ_CP042437.1|WP_090643187.1|1760511_1760766_-|ATP-synthase-F1-subunit-epsilon	gnl|CDD|213395	cd12152, F1-ATPase_delta, mitochondrial ATP synthase delta subunit. The F-ATPase is found in bacterial plasma membranes, mitochondrial inner membranes and in chloroplast thylakoid membranes. It has also been found in the archaea Methanosarcina barkeri. It uses a proton gradient to drive ATP synthesis and hydrolyzes ATP to build the proton gradient. The extrinisic membrane domain, F1, is composed of alpha, beta, gamma, delta, and epsilon subunits with a stoichiometry of 3:3:1:1:1. Alpha and beta subunit form the globular catalytic moiety, a hexameric ring of alternating subunits. Gamma, delta and epsilon subunits form a stalk, connecting F1 to F0, the integral membrane proton translocating domain. In bacteria, which is lacking a eukaryotic epsilon subunit homolog, this subunit is called the epsilon subunit.	1.31693e-25
NZ_CP042437.1|WP_090643183.1|1760851_1762357_-|F0F1-ATP-synthase-subunit-beta	gnl|CDD|236447	PRK09280, PRK09280, F0F1 ATP synthase subunit beta; Validated.	0
NZ_CP042437.1|WP_147052976.1|1767053_1767992_-|DNRLRE-domain-containing-protein	gnl|CDD|366248	pfam00688, TGFb_propeptide, TGF-beta propeptide. This propeptide is known as latency associated peptide (LAP) in TGF-beta. LAP is a homodimer which is disulfide linked to TGF-beta binding protein.	0.00215061
NZ_CP042437.1|WP_147060909.1|1765420_1767016_+|hydroxymethylbilane-synthase	gnl|CDD|234612	PRK00072, hemC, porphobilinogen deaminase; Reviewed.	2.62453e-115
NZ_CP042437.1|WP_147052972.1|1756423_1758163_-|biosynthetic-type-acetolactate-synthase-large-subunit	gnl|CDD|272915	TIGR00118, Probable_acetolactate_synthase_large_subunit, acetolactate synthase, large subunit, biosynthetic type. Two groups of proteins form acetolactate from two molecules of pyruvate. The type of acetolactate synthase described in this model also catalyzes the formation of acetohydroxybutyrate from pyruvate and 2-oxobutyrate, an early step in the branched chain amino acid biosynthesis; it is therefore also termed acetohydroxyacid synthase. In bacteria, this catalytic chain is associated with a smaller regulatory chain in an alpha2/beta2 heterotetramer. Acetolactate synthase is a thiamine pyrophosphate enzyme. In this type, FAD and Mg++ are also found. Several isozymes of this enzyme are found in E. coli K12, one of which contains a frameshift in the large subunit gene and is not expressed. [Amino acid biosynthesis, Pyruvate family].	0
NZ_CP042437.1|WP_147052971.1|1755779_1756382_-|acetolactate-synthase-small-subunit	gnl|CDD|183365	PRK11895, ilvH, acetolactate synthase 3 regulatory subunit; Reviewed.	7.66151e-27
NZ_CP042437.1|WP_147052968.1|1751587_1752178_-|3-isopropylmalate-dehydratase-small-subunit	gnl|CDD|179314	PRK01641, leuD, 3-isopropylmalate dehydratase small subunit.	1.70513e-91
NZ_CP042437.1|WP_147052973.1|1762633_1763980_+|G-D-S-L-family-lipolytic-protein	gnl|CDD|238863	cd01825, SGNH_hydrolase_peri1, SGNH_peri1; putative periplasmic member of the SGNH-family of hydrolases, a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	0.000277307
NZ_CP042437.1|WP_147052961.1|1744074_1745736_-|hypothetical-protein	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	1.74478e-17

Protein sequences

>NZ_CP042437.1|WP_147052970.1|1754420_1755479_-|ketol-acid-reductoisomerase
MAKLNFGGTEENVVTRDEFPLSKAQEVLKDEVVAVIGYGVQGPGQALNQKDNGINVIVGQRKGTKTWDKAVSDGFVPGETLFEIEEALQRGTVICYLLSDAAQIALWPTVKKHLTPGKALYFSHGFGITFNEQTGIVPPADVDVFLVAPKGSGTSLRRMFLQGRGLNSSYAIFQDATGKAFERVISLGIAVGSGYLFETNFKKEVYSDLTGERGTLMGCIQGIFAAQYEVLRSNGHTPSEAFNETVEELTQSLMPLVAENGMDWMYANCSTTAQRGALDWWKKFRDATKPVFEDLYKSVATGFESQRSIDSNSQPDYREKLDAELKELRESELWQAGKTVRSLRPENQVVEA
>NZ_CP042437.1|WP_147052969.1|1752849_1754262_-|3-isopropylmalate-dehydratase-large-subunit
MGQTLFDKIWDAHVVSSNEGFPDILYIDTHFIHEVTSPQAFDGLRTRGLPVFRPKQTVATADHNVPTIDQHLPIKEELSRYQVDMLTKNCAEFGIELYGLGHPFQGIVHVIGPELGITRPGGTYVCGDSHTSTHGAFGAIAFGIGTSQVEQVMATQCLLQSRPKRMKIEVNGKLQKGVGAKDIILYIISKISAAGGTGYAVEYAGDTIRALSMEGRMTICNMSIEMGARCGLIAPDDTTIEYVKGREFAPKGEEWDKAVAYWKTLYSDEDALFDEVLSFKAEDIEPMITYGTNPGMGIGVTQHVPETASFEAKEQGSYKKALDYMGLHDDEQLLGKPIDYVFIGSCTNSRIEDLRQVAEFVKGKHKADNVTVWVVPGSKQVQEQAIREGLDKIFNEAGFPLREPGCSACLGMNEDKIPAGKYCVSTSNRNFEGRQGPNSRTFLASPLTAAASAITGKVTDIRSFLSESVV
>NZ_CP042437.1|WP_147052968.1|1751587_1752178_-|3-isopropylmalate-dehydratase-small-subunit
MSTKIFKHIQTSVVPLPIENIDTDQIIPARFLKATTREGFGNNLFRDWRFDENDNPKQDFVLNNPNYSGKILVAGKNFGCGSSREHAAWAIADYGFDAVVSSFFADIFKGNALNNGLLPVQVSEDFLKKIFDAVYADEHAVVEIDLVDQFIRLVPTGEQESFEVNPYKKACMTNGYDDIDYILSKKELIAEFESER
>NZ_CP042437.1|WP_147052967.1|1750683_1751478_-|methyltransferase-domain-containing-protein
MNKTIHREGKGTAKLFDERSLANDYATLTSALKPGLRVLDVGCGTGAISKDIAAKVGDTGHVTGIDNTEFFIQSGKETYADVKNLDLIYTDLFAYEPEGQFDLIVAARVLQWLNNPVEALKKMYSLLKPGGTVSILDYNHEALEWQPQPPPSMLRFYATFLRWRGDAGMNNHIAEDLPGYFEEAGFINIAEFNADEVYQKGEENFTNKAGIWAKVAMSKQMVEEGYIDDELRLLAIDEYTEWVATDAGRMVMKLKEIRGIKPLS
>NZ_CP042437.1|WP_147052966.1|1749538_1750630_-|3-isopropylmalate-dehydrogenase
MKKHILVIPGDGIGPEVTTWGKAVLEKIGHDFGHEFTFDEALMGHAGIEATGNPLPDETLAKAKASDAILFGAIGHIKYDNDPSAKVRPEQGLLKIRKELGLYANLRPIMLFDELLDASSLKPEILKGTDILFFRELTGDVYFGEKKRSEDRNTASDLMIYSRYEVERIAIKAYEAAMVRGKRLCSVDKANVLEASRLWREVVQEIAKNYPEVETEHMFIDNAAMQLVKNPKKFDVVLTANLFGDILTDEASQIAGSMGMLASASIGDGTGFFEPIHGSAHDIAGMDKANPLASILSVALMLEISFGLKDEAKLITSAIDKTLKEGYRTGDIADANTDKAKILGTKAMGQKVLEYLAPPNPPR
>NZ_CP042437.1|WP_147052965.1|1748657_1749413_-|methyltransferase-domain-containing-protein
MKWNADLYDQKHSFVFQYGEDVLALLDVKPGEHILDIGCGTGHLTKQIQDKGAIVKGTDYSPDMIAQAKKLFPGVDFAVENAADFYTEQKYDAVFSNAALHWVLDANGAIKSIYNALKPGGRFVAEMGGKGNVAKLLEAIRLVLQNHGYPDKAETKVWYFPSTAEYAKLLEDHGFRVTFTAHYDRKTPLQDGDQGVAKWVTMFGAQFLEGIPEEEKEQILAEITKKLEPYYNENGQWYADYKRLRFVAVKE
>NZ_CP042437.1|WP_147052964.1|1747384_1748551_-|2-isopropylmalate-synthase
MLHDPNRVYVFDTTLRDGEQVPGCQLTPPEKIEIAKELELLGVDIIEAGFPVSSPGDFQSVVEISKAVTNPTVCALTRANKGDIDAAIESLKYAKHPRIHTGIGSSDMHIKHKFNSTREEILERAVEAVKYAKRAVEDIEFYAEDAGRADVVYLAQMVEAVIAAGATVVNIPDTNGYCLPDQYGAKIRFLKENVKNIDKAIISVHCHNDLGLATANSIAGLQNGARQIEGTINGIGERAGNTSIEEVVMILKVHQVLGLKTNIDSKRFYELSQMIRTQMRMPVQPNKAIVGSNAFAHSSGIHQDGFLKMRENYEIIRPEDVGFPSATIVLTARSGRHALKFHLERLGFSLDKEELAQVYNKFLTLADVKLDINDEDLQGLMAHRLVKN
>NZ_CP042437.1|WP_147052963.1|1746131_1747382_-|threonine-ammonia-lyase-IlvA
METETKSLLDFDSAYERLKGVVKRTPLEYNAGLSAKYECELYLKREDLQIVRSYKLRGAYNMISQLTQDELDRGVVCASAGNHAQGVAFSCSRLGTKGVIFMPEITPKQKVTQTEMHGKGNIEIILTGDTFDDCLREALIYTEAHQMTFIPPFDNYRIIEGQGTVGVEILQDLPGIEAIVMPIGGGGLAAGTGTYLKQHVPGIYLVGVEPEGAPSMLEAFEHGGPTTLKEINRFVDGAAVKCVGKLTYNLCHEVLDEMLLVPEGKVCTTILKLYNEDAIVVEPAGALSVAVLDACKDKIKGKKVVCVISGGNNDIARMQEIKEKSLLYEGLKHYFIVRFPQRPGALKLFVNNVLGPQDDITRFEFIKKTEKENGPALVGIELRNAGDYPALLNRMAAHRFDVIELNKDQTLFEYLV
>NZ_CP042437.1|WP_147052962.1|1745742_1746135_+|hypothetical-protein
MKIVKGYLNKLTIKLQTKNYNQNSLVIKVITNISVLWDAETSSARLGSKQKASRSFCLREALIFWGNRLGLNGMRGVCFVPRNDMVGLAWRLCMAARPLPTCFDRLSMTGSFYLLPFTFRLLPFTFTLSP
>NZ_CP042437.1|WP_147052961.1|1744074_1745736_-|hypothetical-protein
MVTKQLPLLVFLIFANLFTTLLTAEAQVKKARPQSVPDIYMAGVGNGNGEYYMASYFKNMKPGLPLTGADESTKESYGAAICVVGNDVYIAGCLGRKAVYWKNGQLVQLASTSVSYGAASAITVAGNDVYVGGTGYKKLFLHDGSKGRDQEQPRYWKNGQEVLLPQPLEDNGYENETTIVSMKVVGDDLYIIGRVAYGYGPIYWKNGQLVQSLNNGLDRVEKIEVVNGNVYAVGSKDSKAAYWKNGTTTILTSEESLATAIAVAGNDVYVTGIIGSYKMKGLYPGYGNGGVGKYWKNGRQMGLTGGADQYASPYPKSIAVSGNDVYIVGIDQSNSNYMLWKNGQYTALTNNNSRDGWFGPWAITAGAPGGVKGYNATVKTTPPKPQPAPARSSATTPPPTPAAPPAPAPPVQPSNATAIKVQQAARYLADNKLKPGVTTTASGLQYEILQPQAGIKPTLSDKVSYKFKRTMIVGNQVMRAEGLAGPVNLSMTFLAPGLGEGLKLMSPGSKYRFTIPPSLGADTQLRDRPADPNFPLGAVIMIFEVELLEILSK
>NZ_CP042437.1|WP_147052971.1|1755779_1756382_-|acetolactate-synthase-small-subunit
MTQDTEKQEFNITVYTENQIGLLNRIAIIFTRRKINIDSLNTSPSEIESIHRFNIVITESEDVVRKLTRQIEKQVEVLKCYYHTNEDVIWQEMALYKVSTDVIAEKVSVERLLRENGARAVVIRKDYTVFETTGHREETDNLISILQPYGLIEFVRSARVAIIKDSDGFNRKLREFERLEPGEDVIENEYLNQGQKVFTM
>NZ_CP042437.1|WP_147052972.1|1756423_1758163_-|biosynthetic-type-acetolactate-synthase-large-subunit
MEAIQEVLTETKPTETIVEVSGSVALLEALIVEGVDTIFGYPGGAIMPIYDALFDYNDKLNHILVRHEQGGIHAGQGYARTSGKVGVVFATSGPGATNLVTGLADAQIDSTPLVCITGQVFAHLLGTDAFQETDVINITTPVTKWNYQVTDANEIPEVIAKAFYIAKSGRPGPVLIDITKNAQIQLFNYKGYTPCNHIRSYRPKPIVRPQYIQEAAALINQAKKPFILFGQGVILGSAEQEFKTFVEKSGIPAAWTVLGAGAIPTDHPLNVGMLGMHGNYGPNVLTNECDVLIAIGMRFDDRVTGRLDKYAKQAKVVHLDIDPAEIDKNVKSTVPVWGDCKETLPLLTALVDEKQHTEWLAKFNDYTRQEVEQVIEKELNPTTAEMTMGEVIKQLNEITKGEAVIVTDVGQHQMVACRYAQFNNTRSNVTSGGLGTMGFALPAAIGAKFGAQDRTVVAIIGDGGFQMTCQELGTIMQSGIDVKIIILNNRFLGMVRQWQELFNSRRYSFVDIQSPDFVALAAAYRIPGKVIDDRKDLPSALNEMLSNKGSFLLEVMVTKENNVFPMVPQGCSVSEIRLK
>NZ_CP042437.1|WP_147060908.1|1758272_1759955_-|dihydroxy-acid-dehydratase
MELNKYSKTFTQDPTQPAAQAMLYGIGLTDDDMRKAQVGVASMGYDGNTCNMHLNDLAKIVKQGIWDEDMVGLIFHTIGVSDGMSNGTEGMRYSLVSRDIIADSIEAVTGAQYYDGLITLPGCDKNMPGSVMAMGRLNRPSIMVYGGTIKPGHWKGEDLNIVSAFEALGKRMAGTIEDVDFMGIIKNACPSAGACGGIYTANTMAAAIEALGMSLPYSSSNPALSEDKKAECLAAGKAIKILLEKDIKPSDIMTREAFENAMVIIMVLGGSTNAVLHLIAMAKSVDVKLTQDDFQTVSNRIPVLADMKPSGKYMMEDLHNIGGVPAVMKYCLAQGWLHGDCLTVTGKTITENLADVPELEFDTQKIIWPVEKPVKATGHLQILYGNIAEGGSVAKITGKEGTHFEGPARVFDGEFELIHGIQSGRVKKGDVVVIRNVGPKGAPGMPEMLKPTSAIFGAGLGSSVALITDGRFSGGTHGFVVGHITPEAFDGGAIGLINDDDKIIIDATTNTINVILSDEEMAARKAAWKQPALKATKGLLYRYAKTVSSAAEGCVTDEMP
>NZ_CP042437.1|WP_090643187.1|1760511_1760766_-|ATP-synthase-F1-subunit-epsilon
MTLEILTPDKKIYEGEATSVTVPGTLGLFEILNHHAPIISTLQDGKLVVRGGNAGKEEVFFIKGGVVEALNNKVIILAEGILHK
>NZ_CP042437.1|WP_090643183.1|1760851_1762357_-|F0F1-ATP-synthase-subunit-beta
MPNIGKISRIIGPVVDVSFADDAHLPKIYDALEITKDNGQKIILEVQQHLGEDRVRAIAMDSTDGLLRGMKVLDLESAIKMPIGENIKGRVFNVVGDAIDGIPDLDKTNGRPIHNTPPRFEDLSTETEVLFTGIKVIDLLEPYVKGGKIGLFGGAGVGKTVLIQELINNIAKAYAGLSVFAGVGERTREGNDLLREMLEAGIIKYGDAFMHSMEEGGWDLSKVDTEMMKDSKATFVFGQMNEPPGARARVALSGLTIAEYFRDGDEDGKGRDILFFIDNIFRFTQAGSEVSALLGRMPSAVGYQPTLATEMGTMQERITSTKRGSITSVQAVYVPADDLTDPAPATTFAHLDATTVLSRKIAELGIYPAVDPLDSTSRILSPAILGDEHYNTAQRVKETLQRYKELQDIIAILGMDELSEEDKLVVSRARRVQRFLSQPFHVAEQFTGLKGVLVDIKDTIKGFNMIMDGEVDEYPEGAFNLVGSIEDAIEKGKKLLAEANN
>NZ_CP042437.1|WP_147052973.1|1762633_1763980_+|G-D-S-L-family-lipolytic-protein
MRLAGVLFFSALLFFSACKLDTTIGPEKKAETSGSTPTTNTGFYSRYIAIGDSQTAGYTNDGLYNWGIYNSFPNIFAGSLEGSGLKTFNQPLFSIAQMNGTGFMELKGTDANGQPLIVRDTLKTAIRGSINISGSGTMQLLSKFTGDNDNFGVAGLKVADISNTQTGNTNRYFERLLPLNAPANNTSYVDFITSKPFGFFTLNLGTNDVFGYAAGGGVKPLALTDKTTFNTSYTLLVNKLTANGAKGVLTTIPDVSALPFFTATKLADILTKAKVISPTFDKLYIEAKQSIDVGQDGYEVRAATSADLLLLSLNVSQIGKQVSTTHGAQYYGLSPYAPIENKWILDVNEKTIASDYITAYNTSIRTLASTKALALFDAYAFFNDVKKGTTVQGISVSSNYLTGGLFSLDGVHLSPRGNAILANMYVAVTNAKYGTTLKEAKLSDYSAN
>NZ_CP042437.1|WP_147052974.1|1763964_1764963_-|zinc-binding-dehydrogenase
MKAVIITRPGDPSVLQVQERPEPAYADNEVLIKVMAAGVNRPDVFQRKGNYPPPAGAPQDIPGLEIAGVVVAIGATVTHLMVGDKVCALVAGGGYAEYCNAPEEQCLPIPENLSFTEAASLPETFFTVWSNVFDRAGLKDGETLLVHGGSSGIGVAAIQMAKALGHTVYVTAGSADKCRFCEALGAAKAINYKTENFADVINDITAGKGVDVILDMIGGDYTTGNIKSLAVEGRLVLINAMNGSNVQIDLAQVMRKRLVITGSMLRSREVEFKGAIAHKLKAIIWPLLASGKIKPIINAVFPASEAEKAHQLMESSGHIGKIVLDFDYQFAL
>NZ_CP042437.1|WP_147052975.1|1765039_1765252_+|hypothetical-protein
MERIQLVQEALNQIESDYYSFFEETNSGIIDYVNIISNGESNWLNVVVKENSKLPTKIEEAIKDKFKIYQ
>NZ_CP042437.1|WP_147060909.1|1765420_1767016_+|hydroxymethylbilane-synthase
MDRKLIIGTRGSELALWQANFVKDSLAAINITAELKIIKTQGDRILNLSFDKLEGKGFFTKELEEELLAGSIDLAVHSHKDLPTENPPGLIIAAVSEREDPSELLLILKDCVDVHQKLSVKYGAIVGTSSNRRKAQLLAYRPDLEIEELRGNVPTRIGKLRDEKYDAIMLAKAGVSRLNIDLSEFHVEELTPAELIPAPAQGALAIQIREADQELFEAMQALHHADVAEELAVERTVLKLFGGGCHLPLGCYCRKEDDVYQVFTSKANEGDEFPDRVFLKSDTTEGLAQKVVAMFDTNRKLAQSVFITRDLSEQSYFRKALEKHGINIDARSLIRTVPVINKLDPYILRDINWIFFSSKNAVEYFFALKPQLPSKVKFGVMGSGSEDTLRRNGYFAAYVGESGDTAEVAADFAALANGTKVLFPGAEGSLRSIQQGLSAETKIIDLTVYETVIEEDVEGTGADVLVFTSPSNVEAYFQDNLLEPNQQVIAIGKSTGKKFDEMGTRYTLPFSPDEVGLAEAVFGTTCLTNRC
>NZ_CP042437.1|WP_147052976.1|1767053_1767992_-|DNRLRE-domain-containing-protein
MKTHKLIPVTGLIVFFALAACQKNTVTPTVQKVVAKAEPDVTITLPKDSVLLTGTDGNPADVAVGYLWSQISGPGEASIVNESSASATAKHLVEGKYLFQFMVIDNNGLSGVDTVGVIVKGPTITTLDLSPTNNPNETNVGIYNGQDASNHTSIEEPLCAWTINFIPITVRNLLKFDLSSIPANATITSAQLYLYSDTIPKNGDLVHANSGTDNSFVVQQVATDWSTASVTWFNQPAGLTANQVILPSTNQPFLNMNINVKDMVSSMVSSNANYGFKLFVQNEVLYTCRIFCSSYYSDPSRHPRLIVKYIKH

Crispr_ID: NZ_CP042437_3

• CRISPR_ID: NZ_CP042437_3
• CRISPR_location: 1795025-1795120
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_3

Consensus_repeat	Method
ATAAGTTTGGCTTGTTTTAAAATGTA	CRISPRCasFinder

spacers of NZ_CP042437_3

>3.1|1795051|44|NZ_CP042437|CRISPRCasFinder
AATGCTACCGCGGGTTTAGTGAAGCGTAACCCGCGGCAGCATAC

CRISPR arrays and Neighbor proteins around NZ_CP042437_3

CRISPR arrays

The CRISPR arrays of NZ_CP042437_3

>merge|NZ_CP042437|3|1795025-1795120|CRISPRCasFinder
ATAAGTTTGGCTTGTTTTAAAATGTAAATGCTACCGCGGGTTTAGTGAAGCGTAACCCGCGGCAGCATACATAAGTTTGGCTTGTTTTAAAAGTAC

>NZ_CP042437|3|3|1795025-1795120|CRISPRCasFinder
ATAAGTTTGGCTTGTTTTAAAATGTA	AATGCTACCGCGGGTTTAGTGAAGCGTAACCCGCGGCAGCATAC
ATAAGTTTGGCTTGTTTTAAAAGTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147053001.1|1792819_1793707_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052996.1|1787345_1788125_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053007.1|1802329_1802731_+|hypothetical-protein	unknown	unknown	gnl|CDD|319914
NZ_CP042437.1|WP_147052997.1|1788224_1789175_+|TIGR01212-family-radical-SAM-protein	unknown	unknown	gnl|CDD|224163
NZ_CP042437.1|WP_147053006.1|1801882_1802278_+|hypothetical-protein	unknown	unknown	gnl|CDD|367555
NZ_CP042437.1|WP_147053010.1|1804815_1805127_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147052999.1|1790243_1791476_+|acyltransferase-family-protein	unknown	unknown	gnl|CDD|224748
NZ_CP042437.1|WP_147053005.1|1801438_1801756_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053003.1|1795121_1796858_-|ubiquinone-dependent-pyruvate-dehydrogenase	unknown	unknown	gnl|CDD|180614
NZ_CP042437.1|WP_147052998.1|1789203_1790076_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053000.1|1791450_1792809_+|prolyl-oligopeptidase-family-serine-peptidase	unknown	unknown	gnl|CDD|225989
NZ_CP042437.1|WP_147053012.1|1806614_1808666_-|(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase	unknown	unknown	gnl|CDD|179361
NZ_CP042437.1|WP_147052992.1|1783330_1783705_+|DoxX-family-protein	unknown	unknown	gnl|CDD|226720
NZ_CP042437.1|WP_147053008.1|1802736_1803468_-|response-regulator	unknown	unknown	gnl|CDD|225818
NZ_CP042437.1|WP_147052994.1|1785317_1786148_+|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|378924
NZ_CP042437.1|WP_147053011.1|1805687_1806605_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378964
NZ_CP042437.1|WP_147052993.1|1783781_1785308_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|143598
NZ_CP042437.1|WP_147053009.1|1803442_1804576_-|histidine-kinase	unknown	unknown	gnl|CDD|225814
NZ_CP042437.1|WP_147052995.1|1786224_1787220_+|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|293841
NZ_CP042437.1|WP_158642858.1|1796952_1801221_-|response-regulator	unknown	unknown	gnl|CDD|236848

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147052993.1|1783781_1785308_+|GNAT-family-N-acetyltransferase	gnl|CDD|143598	cd07574, nitrilase_Rim1_like, Uncharacterized subgroup of the nitrilase superfamily; some members of this subgroup have an N-terminal RimI domain (class 12 nitrilases). Some members of this subgroup are implicated in post-translational modification, as they contain an N-terminal GCN5-related N-acetyltransferase (GNAT) protein RimI family domain. The nitrilase superfamily is comprised of nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes, which depend on a Glu-Lys-Cys catalytic triad. This superfamily has been classified in the literature based on global and structure based sequence analysis into thirteen different enzyme classes (referred to as 1-13), this subgroup corresponds to class 12. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer.	2.56958e-141
NZ_CP042437.1|WP_147052997.1|1788224_1789175_+|TIGR01212-family-radical-SAM-protein	gnl|CDD|224163	COG1242, COG1242, Predicted Fe-S oxidoreductase [General function prediction only].	1.08293e-102
NZ_CP042437.1|WP_147053012.1|1806614_1808666_-|(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase	gnl|CDD|179361	PRK02048, PRK02048, 4-hydroxy-3-methylbut-2-en-1-yl diphosphate synthase; Provisional.	0
NZ_CP042437.1|WP_147052999.1|1790243_1791476_+|acyltransferase-family-protein	gnl|CDD|224748	COG1835, COG1835, Predicted acyltransferases [Lipid metabolism].	1.57867e-29
NZ_CP042437.1|WP_147053003.1|1795121_1796858_-|ubiquinone-dependent-pyruvate-dehydrogenase	gnl|CDD|180614	PRK06546, PRK06546, pyruvate dehydrogenase; Provisional.	0
NZ_CP042437.1|WP_147053007.1|1802329_1802731_+|hypothetical-protein	gnl|CDD|319914	cd07251, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	7.08328e-17
NZ_CP042437.1|WP_147053000.1|1791450_1792809_+|prolyl-oligopeptidase-family-serine-peptidase	gnl|CDD|225989	COG3458, COG3458, Acetyl esterase (deacetylase) [Secondary metabolites biosynthesis, transport, and catabolism].	2.19835e-35
NZ_CP042437.1|WP_147052992.1|1783330_1783705_+|DoxX-family-protein	gnl|CDD|226720	COG4270, COG4270, Predicted membrane protein [Function unknown].	4.40229e-13
NZ_CP042437.1|WP_147053008.1|1802736_1803468_-|response-regulator	gnl|CDD|225818	COG3279, LytT, Response regulator of the LytR/AlgR family [Transcription / Signal transduction mechanisms].	9.38811e-43
NZ_CP042437.1|WP_147052994.1|1785317_1786148_+|alpha/beta-fold-hydrolase	gnl|CDD|378924	pfam12697, Abhydrolase_6, Alpha/beta hydrolase family. This family contains alpha/beta hydrolase enzymes of diverse specificity.	2.85647e-10
NZ_CP042437.1|WP_147053011.1|1805687_1806605_-|helix-turn-helix-domain-containing-protein	gnl|CDD|378964	pfam12833, HTH_18, Helix-turn-helix domain.	1.25807e-20
NZ_CP042437.1|WP_147053006.1|1801882_1802278_+|hypothetical-protein	gnl|CDD|367555	pfam03544, TonB_C, Gram-negative bacterial TonB protein C-terminal. The TonB_C domain is the well-characterized C-terminal region of the TonB receptor molecule. This protein is bound to an inner membrane-bound protein ExbB via a globular domain and has a flexible middle region that is likely to help in positioning the C-terminal domain into the iron-transporter barrel in the outer membrane. TonB_C interacts with the N-terminal TonB box of the outer membrane transporter that binds the Fe3+-siderophore complex. The barrel of the transporter, consisting of 22 beta-sheets and an inside plug, binds the iron complex in the barrel entrance.	5.27143e-10
NZ_CP042437.1|WP_147053009.1|1803442_1804576_-|histidine-kinase	gnl|CDD|225814	COG3275, LytS, Putative regulator of cell autolysis [Signal transduction mechanisms].	1.56795e-29
NZ_CP042437.1|WP_147052995.1|1786224_1787220_+|MBL-fold-metallo-hydrolase	gnl|CDD|293841	cd16283, RomA-like_MBL-fold, Enterobacter cloacae RomA and related proteins; MBL-fold metallo hydrolase domain. Derepression of the romA-ramA locus results in a multidrug-resistance phenotype. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) from which this fold was named are only a small fraction of the activities which are included in this superfamily. Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	5.895e-70
NZ_CP042437.1|WP_158642858.1|1796952_1801221_-|response-regulator	gnl|CDD|236848	PRK11107, PRK11107, hybrid sensory histidine kinase BarA; Provisional.	2.18733e-121

Protein sequences

>NZ_CP042437.1|WP_147053001.1|1792819_1793707_+|hypothetical-protein
MDKNLTLNKKLFKYLLAVLILIAFAPRYSYADGFPVRPGRFILSPSVSYFFANKQFDSTSHRRAFDDNGRFHSVSYAFYSEYGISRKFTLSALVPYSMNYFNTDSITHAITTSGLQDIEIGLKYYLANINYKYYFSIKATGIIPTYRNNASLGYGYYGSELKLAFAGSGHLFGKQSYFVAENAVREYFGSESVFQDRYNLTYGLTLDKKFREQFSISIGGFYATSNNSFINPNPIISANPNTSKNFAFNQVSASYGHAFTKNLSLFLTGGTFITGRNTGAGTSLSASLNYRLDTR
>NZ_CP042437.1|WP_147053000.1|1791450_1792809_+|prolyl-oligopeptidase-family-serine-peptidase
MSRKTSMLSEYNMVRKLKRYFILIGALFAFQQVFAQHDSPVNPKKEDDESVSTILNINNKDGIFNSVASFTFDVKNTYDTQQEGTVSYLITDEKGVKIKTLSKPVKIERKSTEHYSFEIPALKTGFYKLNMMINVSDYDDTTRRAFGIRADEVKSAFPKPADFDSFWANAKAELAKVKPQFKVTEDVSQNTDNRRVFLIEMKSLDNLTIRGWMTIPKNNNKNKQFSVLLGLPGYQVTLKPIVGRDDDLAIITLNTRGQGNSRDVIHTERDAFISYNIEDRDKYVMRGVIMDCVRAVDFIYSRKELRHDQILATGGSMGGYLAIALAALDKRVTICSAQNPILSDVHNLVGTVEWPIKDIRKYVAGKPGVTFDQVLHNMEYYDTKNFATDIKCPILLGLGLLDPYVPPGNGFAVYNSLNTDKKVMVFKDLGHEVSQKYKDYEGAWMRDTFGLF
>NZ_CP042437.1|WP_147052999.1|1790243_1791476_+|acyltransferase-family-protein
MSQRAQQNYIPALTGVRAMAAYLVFISHFAYVFDEKFPHSVQRFFNEFHIGVTIFFVLSGFLIAFRYFDSFKLTKDWFKQYLKNRVARIYPMYAILTIGAFIAFYFTNNQIVTAGHNPIAMFLMNIVFLRGFFDQLKFTGVAQGWSLTVEECFYFSAPFIFLIATKYKKFYIQPIAVTGLGVVLVLIFSHVNWYGFFGNFTFMMLYTFLGRCFEFFAGIQLALIVRRQKPDGSSKKKLTYLGFFLIFFCVWIMSVLPIPKGQEAGLHNPLGIITNNYLLALSITLFFYGILTETTLLKKVLATPFVELLGKSSYIFYLVHLGYMYNFLHFGFNWLNDYTFALYDKWGVEWHSPFEYDSLNLLYAFIVLNIISITLFKLIEEPLNHYIRKSDFLIKNKSRKPENEPENINA
>NZ_CP042437.1|WP_147052998.1|1789203_1790076_-|hypothetical-protein
MRKLLPSLLLLFCFNNLRGQEIIEQFLGIDNFPNKFIIANKVVRRVKYEYKLNGHGIADSTYMGAINFNYNNEGHLTDQVHFDKDNYLDEKYVYFYYDFGLISKKIEYEYPKRKLYPRSLNVTHEFAYDSIGRLQYHVSYNQDTLFVNRDKRDYDAKGRLYRITKTTNNLPTYVSNMASYNEDNNLEVIDYFYKQNTPDFSYKMNTDTTEQGDKIINISKIVPGKDEDYWCTYKFNRYNQCTEIIGFDVVGLQKTKYTEKLIYNTDGTLYTMIFYINKKMRSMYKFYYHK
>NZ_CP042437.1|WP_147052997.1|1788224_1789175_+|TIGR01212-family-radical-SAM-protein
MQLTGEKTAIWEKGYNNYGPWLKEKYKGHRVFKVIVDGGFTCPNRDGSKGYGGCTYCNVDSFTPSVSRNAPTVRQQVIEGMERARKGNKADKFIIYFQPNTNTYAPAHYLKMMYDEALSYGTEDIVGLSVGTRPDCIDAEKIALLESYTDRFDVDLEMGMESIYNETLGQINRGCSHEELVKALKLVENSKLDICVHTIFGFPWETHEMMLKYADEINRFPQIKFVKFHHLHIVEGSVMGVKYKREPFKLFGIDEYADFLCELLPRVRPDIVIQRLFGLSDRELLIAPNWGLKKSEIQYYIDQRILSRGVVQGSAL
>NZ_CP042437.1|WP_147052996.1|1787345_1788125_+|hypothetical-protein
MQATTIDEIITQLETIITDAIQTGSRAGYFAALYHKVTCKVKEGILAGEFEDGKRMEQLDVTFASRYITAYHQWQQKQQPSASWALAFGIFNKPRKMVLQHLLIGMNAHINLDLGIAVVETARAFNQSLTQVHNDFNAINTILSALTYEVITELNQVSPLMSLAGLHAQNNSILIQFALGNARDGAWCFAEDLYTRTGQDYINLISSRDADINKLGLGIVAPVGLLSFTVWIIHLFEWRNPSKITTVLSEYKKAYLKVN
>NZ_CP042437.1|WP_147052995.1|1786224_1787220_+|MBL-fold-metallo-hydrolase
MSLEASRKKAKKYINVIPTDEAGFGKMIPILREYMGNKAENSPKKPIGPFKTDVKIYNDAPESGLRITWVGHSSILIEIDGKRILTDPVWGDRASFSKYFGPKRFFKPAIALQDLPPLDAVLLSHDHYDHLDKETIKFFAGTDIPFYCSVGVGQYLEKWGIFKNFVFEMDWGDSVLIGNQVVVTSTPSRHFSGRGVVNRNETLWASFVIKGPKHNIYFGADSGWSPSFAEIGKAFGPFDLTMLEVGAYGKYWPDIHMGPDHASNAHIALKGKLMMPIHYGTFNLAPHAWYEPVERLEKFAKDKKIDLFVPEPGKPTEVKGPYNSAWWKKFM
>NZ_CP042437.1|WP_147052994.1|1785317_1786148_+|alpha/beta-fold-hydrolase
MIRKDNYTLPGAKGRPMLIDVTYNDAFKNAPVVIFAHGFKGFKDWGTHNLVAGYFANAGFKYLKFNFSHNGTTPDNPLDFTDLIAFSDNTFSIELEDLDTIIDFACSGSGMAAASGVYLIGHSMGGGISIVKSAEDSRIKKLVTMASISSFYNLWPEEIEIQWRLQGIIYMPNKRTGQQMPLKATLLGDLDKHPKRLDILAQAAKVKQPWLLMHGDTDQTVPLSHAEELYAAHPDAEFFILPGGDHTFGGAHPYLSDVLPASLIAFCDTTISFLSK
>NZ_CP042437.1|WP_147052993.1|1783781_1785308_+|GNAT-family-N-acetyltransferase
MDLQSVEMRNLEVHDYQELKKSMKSAYMDMDEDYWDANSIKKLIKIFPEGQICVTVNDVVVGCALAIIVDYQKFGDNHTYKQITGDSTFKTHTDKGDVLYGIDVFIHPNYRGLRLARRLYDARKALCEKLNLKSIIAGGRIPNYQKFQNDLTPRQYIDKVKYKEIYDPTLSFQLANDFHVRKVLRNYLPEDSRSKGFATLIEWNNVYYEEISNAINQKTVVRIGLVQWQMRPYNNISELLKHAEYFVDAVSDYQADFILFPELFGTPLMADYNHMDSAKAMRELAKYTQPIIEEFSKLAVSYNVNIIAGSMPTIFEDSLYNVSYLFRRNGSMEEVYKIHPTPSEISSWGIRGGDEVRVFETDAGKIGILICYDVEFPELSRILASQDMQILFVPFLTDTQNGYNRVKFCSQARAVENECYVAIAGCVGNLPNVNNMGISYAQSAVFTPSDFGFPTNGIQSEATPNSEMIVIADVDLSLLDELHEYGSVQNLKDRRTDLYNITFNGKKV
>NZ_CP042437.1|WP_147052992.1|1783330_1783705_+|DoxX-family-protein
MRFVKKVSLFILVVGYAFAGINHFLNPESYIHIIPRYIPFPVLMNIIAGVAEISFALMLIRPKTRPWAIYGIILMLAAFLPVHIQMLIDAPFKLANITVTPLIAWVRLILQPALMLWVWWHRKN
>NZ_CP042437.1|WP_147053003.1|1795121_1796858_-|ubiquinone-dependent-pyruvate-dehydrogenase
MAKKVADQLVQMLVDAGIKRIYAVTGDSLNEVNDAVRREGSIQWVHVRHEEAGAYAAGAEAQLNGLACCAGSSGPGHVHLINGLYDAHRSGAPVIAIASTIASFEFGTNYFQETNTIKLFDDCSYYNQIATTPKQLPRMLQAGIQSALHQKGVAVIGLPGDLAAMDAVEIETSIQNFTPAPVVRPTDADLYELAALVNRYNKITIFCGIGAAGAHDQVVELSQKLNATVAYSFRAKMDIQYDNPNEVGMTGLLGLPSAYHSMHECDLLILLGTDFPYTPFMPADCKIVQVDIKPERLGRRAKVDVGLCGTVKDTLIALLPLISQKQDNSFLQAQLKVYADVKDKMQTYVDNSGETDKIHPEFVAHVLDKLAAGDAIFTVDTGMSCVWGSRYINATGKRQMIGSFNHGSMANAMPQAIGAALARPAQQVIALCGDGGLSMLLGDLATIVQYKLPVKIIVFNNRSLGMVKLEMEVAGLPDWQTDMYNPDFALVSQAMGIKGFTVTEPGDVRQAISNALAFDGPALVNVFTDPNALAMPPKIELKQVAGMAVSMTKLMLNGHMDEVLDTVKANYKHLKDLL
>NZ_CP042437.1|WP_158642858.1|1796952_1801221_-|response-regulator
MFTILLSPKDGKTQAPEIKFKQISIEQGLSNSYVFATRQDSRGFMWFGTQDGLNRYDGQQMVVYRNIPGDKHSLSDNLIKYIYEDSNKILWIGTVNGLNSFNPYSNSFARYTHDAKDKNSISGNMIACIFEDTQHVLWVVSEDGGLDIFNRQTKQFLHFAHSKKDGNSISAGSVHYILEDRQNRLWIATDSGLNVYNRSAKKFNLVKNKLGSAANNIQSMQLARDGKLWLATKTAGVLVFDPQNSSFKQYQHITGSAGSLSGNEIALAGLLIDHEGHVWVGTINEGLNLYNPADDSFYHYTHKFYDPTSLAQTSASGLFEDNQGNLWVGTGRGGISLYTPAANRFNVYRQEKDPNSLSFSDVKSFCEDSRGYIWIGTDGGGLNLFNREKATFKHFRYNEADAASIGSDAVLDITEDLDKNLWISTWAGGLNLLRPGSTRFTRFKNNPNDKTTISSDMVFKTFQDSEGNLWVGTFGGGLNLLDAKTHQFRRVTKDPDGVTEFLGNNVFVINQDKAGNVWFGGDDGGLNCYNLKSRRFSHYFNELAKKPDIRVIFTDHKGRLWIGQTGLYLFDAKKNAFALYNKQPGQFDDMIKGITEDEFGNLWVSANDGLSMFNPDKHTYKKFNIHDGLQGIEFESNSFLRAKDGEMFFGGTKGLTTFYPKNIKINTFLPPVFITGLQIFNKTIVPGEKDSILKTDISLTRQLHLNYRQTSLTFEFNGLNYVIPENNSYAYKLEGFDTSWTTADATKRATYTNLDPGTYTFRVKASNNDGFWNPKTASVRVIITPPYWQTLWFRILAALTFIVGIYSYYRHRIDGINKQKIALEKQVKERTADIANKAEELQTQSEALQAQAEELQAQSEELHSLNTELTIKSDKLLEQADDLKVLNQLLTEQKHQEHLAREEAEKANLAKSTFLATMSHEIRTPMNGVIGMGSLLAETNLDSEQREYTDTIINCGESLLNVINDILDFSKIESGKIEIEHEDFVLRKSIENVMDVFSTKIAEKHIDLIYEIDTDVPACIVGDELRLKQVLINLVSNAIKFTEKGEIFIRVFAASKPHDGNILIGFSVKDTGIGVPENKLSNLFKPFSQVDSSTTRKYGGTGLGLVISKKLVEFMGGEIWVQSLPSEGSVFNFTITAGVSDAKAPRDEMYTTAGFKGVQVLIVDDNTTNLKILKNQLENWGMEVTAATSGKEALNQLVTDSSIQLVITDMEMPGMDGVGLTKAIKSINELIPVIMLSSIGDESRKKFPGLFAAILIKPVKQQYLFNSLQIALNLNNNNSLPEGKSKQILSVDFAVQNPLSILVAEDNPVNQKLIQRILSKLGYAPQMVQNGFEVLTEMEKNDFDVVLMDVQMPGMDGLETTANIRKNSRQQPYIIAMTANAMAEDKEVCLQAGMDNYIAKPMKLNEIIDMLKNVSTTYKQKA
>NZ_CP042437.1|WP_147053005.1|1801438_1801756_+|hypothetical-protein
MARIVIVAYKPKPGKALELKELTKTHVPRLRAEGLVTNREAVIMQAADGTVIEVFEWLSADAIRQAHANPVVHQLWAEYAEVCDYVNLNSLAEAGNMFAEFNAID
>NZ_CP042437.1|WP_147053006.1|1801882_1802278_+|hypothetical-protein
MKFSLLPIIAILAFCFIGQHSFAHEQKDTVKSNTATIEPGEVLPQFPGGQDKLTAFIKSKLRPVKGASGKVLVYFVVEKTGKLNHIKVIKGLSAEANKEAVRVIKLSPKWKPGSQNGVARRVAYTTPVTFS
>NZ_CP042437.1|WP_147053007.1|1802329_1802731_+|hypothetical-protein
MKQVLSAVTIAAKNLQQLRLFYTGVLDWEILTENESVLMLKLKTVVLTLCTEAVFAGYTGIPPRGEKHTGCYFTINLDSAKEVDDNFMALASLKTTIVKMPAQTFWGGYSGFFTDPEDNLWELCHNPIPGTRA
>NZ_CP042437.1|WP_147053008.1|1802736_1803468_-|response-regulator
MKLRILIVDDEPYAIEVMENYLRNFDDMEIVGKCYNAIQAFQLLQQKTVDLMFLDIQMPGITGIDFLKTLKNPPKTIFTTAYSQYALDGFDLNVVDYLVKPIPLDRFMRAIDKVYQLSGNNAGTGHSYEKFGGDTEAFLYLKVERKTIKINVNDILWVESLRDYVKVITTGNVYISKQKISLLEGMLPENKFVRAHRSFIVAIAHISSFYAYSVEVNGHELPIGRNYKQEMQKRLKAENFHFK
>NZ_CP042437.1|WP_147053009.1|1803442_1804576_-|histidine-kinase
MKQLADLDVAHFKMPRPLQHILFWLTVSFIIIMMYSVQTNFMVSLRNNLIFMPIQIAYYYAIAGWLIPKYLFPGRYLKFGCLALGVFVLSVVVTRIVGILFVTPYTIRMMHVTEGDYFEASRRPFLMKLFDLQNMINALKGTNLVIGFVLAIKLFKMWYQRKQATLQAELNALKAQVHPHFLFNTLNNLYALSLNQSAKSPQLILNLSNILRYMLYECNTGEVLLSQEIKMLQQFISLEKLRYEDRLDINFNIYGDTDGKLIAPLLMLPLIENAFKHGAGEQMGDAWININLYVMRDELKLKISNSKAAGANKGAGKTGNIGLQNLRKRLELIYPTTHSLKIMDDHDTFLAVLDVRLNFAPQTPSQITTHEIAYTHS
>NZ_CP042437.1|WP_147053010.1|1804815_1805127_+|hypothetical-protein
MKKTVLTLAIIWMAATGSIAQTKTSNTATWVVESNLNHPGIQTVRFYDSDKHLIYTETIKARINVSNKKVQRKLNSMLDILMTTGKPVNDSNLLAASFKVKKN
>NZ_CP042437.1|WP_147053011.1|1805687_1806605_-|helix-turn-helix-domain-containing-protein
MSDKITVLDIPSTLKKHLASAGDRAPDFGIINDGWNQDDFAVLNNHPGLTHGLPVKTDYYSVILCLRGSCKKTIGHFVFEVYTNSIHLVSPQFITSFEDASPDLLLYEVLFKKEFLINNLLKENILDNLLEVNPDYPPIYGLSQKSCASLKALYEKISDESREKGAFHLPILRLLLTDLLYEMNRACENCLLHSTRHLSKQYQLVYKFKKLVEDQFLTLKTVQEYADALFISAKYLTEIVKAETGQNALHVIHNRMYLEAQYLLSSSGLSIKEIAERLNFDSSSHFSRFFKRFAGNNPSEFKQLQ
>NZ_CP042437.1|WP_147053012.1|1806614_1808666_-|(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase
MNTDAVKLLQGRYCNSLTQYSRFVTREVNIGDVPMGGNNPIRIQSMTTTDTMDTMGTVEQSIRMVDAGCEYVRITAPSIKEAKNLAEIKKQLRARGYNVPLVADIHFTPNAAEVAARIVEKVRVNPGNYADKKKFDQIDYTDLEYQGELERIYQKFAPLVNICKEYGTAMRIGTNHGSLSDRIMSRYGDTPQGMVESAMEFMRMCETLNYYNLVISMKSSNPQVMVQAYRLLVETMVAEGMNYPLHLGVTEAGDGEDGRIKSAVGIGTLLEDGLGDTVRVSLTEEPEAEAPVAIELVKRYSLREKEVKGERLKAKGNEIITDKNLLPFTFHLSPQTHSPYEYKKRHTYEANAFIGGHMVPRVVLDLSKKNLKDPGIMADAGYIYSPLLDKYNMAEQSVDFVYLADELPSFNLPGNLKQLYNYQTWLKLADKTLCHPLFTLKEYIAATNKTSALNLVKLFPEDIDSEDFGSLPFDNSLVFVLETNALHGMADQRGFFFKMEELGLDVPVIVKRSYEFGVMSIESEHENSALKTQNLQLFAATDLGALLVDGFGDGIWIDAPGVDTKVITSTAFGILQATRSRISKTEYISCPSCGRTLFDLMITTQMIRSRTSHLKGLKIGIMGCIVNGPGEMADADYGYVGSGTDKITLYRGKEAVKKNISAANALDELIGIIKDDGNWVEQE

Crispr_ID: NZ_CP042437_4

• CRISPR_ID: NZ_CP042437_4
• CRISPR_location: 1943628-1943729
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_4

Consensus_repeat	Method
ATTGGTTCACTTGTTCATTAGTTCATTGGT	CRISPRCasFinder

spacers of NZ_CP042437_4

>4.1|1943658|42|NZ_CP042437|CRISPRCasFinder
TCATTGGTCTTTTGCGCTGGAATTTCCTGGCAAGTGGCCTGA

CRISPR arrays and Neighbor proteins around NZ_CP042437_4

CRISPR arrays

The CRISPR arrays of NZ_CP042437_4

>merge|NZ_CP042437|4|1943628-1943729|CRISPRCasFinder
TTTGGTTCATTGGTTCACTTGTTCATTAGTTCATTGGTCTTTTGCGCTGGAATTTCCTGGCAAGTGGCCTGAATTGGTTCACTGGTTCATTAGTTCATTGGT

>NZ_CP042437|4|4|1943628-1943729|CRISPRCasFinder
TTTGGTTCATTGGTTCACTTGTTCATTAGT	TCATTGGTCTTTTGCGCTGGAATTTCCTGGCAAGTGGCCTGA
ATTGGTTCACTGGTTCATTAGTTCATTGGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147053112.1|1934747_1934987_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053124.1|1951136_1952474_+|insulinase-family-protein	unknown	unknown	gnl|CDD|223685
NZ_CP042437.1|WP_147053125.1|1952651_1953749_-|AI-2E-family-transporter	unknown	unknown	gnl|CDD|223701
NZ_CP042437.1|WP_158642863.1|1935022_1935277_+|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	unknown	unknown	unknown
NZ_CP042437.1|WP_147053115.1|1937773_1939090_-|DUF3887-domain-containing-protein	unknown	unknown	gnl|CDD|379023
NZ_CP042437.1|WP_147053117.1|1942204_1942594_-|DUF1634-domain-containing-protein	unknown	unknown	gnl|CDD|377927
NZ_CP042437.1|WP_147060918.1|1941921_1942137_-|KTSC-domain-containing-protein	unknown	unknown	gnl|CDD|379296
NZ_CP042437.1|WP_147053111.1|1934258_1934507_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053118.1|1942729_1943566_-|TSUP-family-transporter	unknown	unknown	gnl|CDD|376667
NZ_CP042437.1|WP_147053122.1|1948922_1949621_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053116.1|1939368_1941807_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|379720
NZ_CP042437.1|WP_147053119.1|1943926_1945300_+|insulinase-family-protein	unknown	unknown	gnl|CDD|223685
NZ_CP042437.1|WP_158642864.1|1954397_1954562_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053120.1|1945400_1946702_+|insulinase-family-protein	unknown	unknown	gnl|CDD|223685
NZ_CP042437.1|WP_147060919.1|1954843_1957246_-|DUF4982-domain-containing-protein	unknown	unknown	gnl|CDD|225789
NZ_CP042437.1|WP_147053121.1|1946913_1948761_+|UbiD-family-decarboxylase	unknown	unknown	gnl|CDD|376697
NZ_CP042437.1|WP_147053114.1|1937208_1937697_+|DinB-family-protein	unknown	unknown	gnl|CDD|378981
NZ_CP042437.1|WP_147053126.1|1953916_1954363_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147060917.1|1935335_1937072_-|DUF885-family-protein	unknown	unknown	gnl|CDD|377577
NZ_CP042437.1|WP_147053123.1|1949740_1951120_+|insulinase-family-protein	unknown	unknown	gnl|CDD|223685

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147053124.1|1951136_1952474_+|insulinase-family-protein	gnl|CDD|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	2.36874e-39
NZ_CP042437.1|WP_147053125.1|1952651_1953749_-|AI-2E-family-transporter	gnl|CDD|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	7.56522e-44
NZ_CP042437.1|WP_147053123.1|1949740_1951120_+|insulinase-family-protein	gnl|CDD|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	1.04505e-55
NZ_CP042437.1|WP_147053115.1|1937773_1939090_-|DUF3887-domain-containing-protein	gnl|CDD|379023	pfam13026, DUF3887, Protein of unknown function (DUF3887). This domain family is found in bacteria and archaea, and is approximately 90 amino acids in length.	1.53851e-11
NZ_CP042437.1|WP_147053117.1|1942204_1942594_-|DUF1634-domain-containing-protein	gnl|CDD|377927	pfam07843, DUF1634, Protein of unknown function (DUF1634). This family contains many hypothetical bacterial and archaeal proteins. A few members of this family are annotated as being putative transmembrane proteins, and the region in question in fact contains many hydrophobic residues.	3.05915e-31
NZ_CP042437.1|WP_147060918.1|1941921_1942137_-|KTSC-domain-containing-protein	gnl|CDD|379296	pfam13619, KTSC, KTSC domain. This short domain is named after Lysine tRNA synthetase C-terminal domain. It is found at the C-terminus of some Lysyl tRNA synthetases as well as a single domain in bacterial proteins. The domain is about 60 amino acids in length and contains a reasonably conserved YXY motif in the centre of the sequence. The function of this domain is unknown but it could be an RNA binding domain.	2.04733e-17
NZ_CP042437.1|WP_147053118.1|1942729_1943566_-|TSUP-family-transporter	gnl|CDD|376667	pfam01925, TauE, Sulfite exporter TauE/SafE. This is a family of integral membrane proteins where the alignment appears to contain two duplicated modules of three transmembrane helices. The proteins are involved in the transport of anions across the cytoplasmic membrane during taurine metabolism as an exporter of sulfoacetate. This family used to be known as DUF81.	8.97072e-28
NZ_CP042437.1|WP_147053116.1|1939368_1941807_+|TonB-dependent-receptor	gnl|CDD|379720	pfam14905, OMP_b-brl_3, Outer membrane protein beta-barrel family. This family includes proteins annotated as TonB dependent receptors. But it is also likely to contain other membrane beta barrel proteins of other functions.	1.76597e-100
NZ_CP042437.1|WP_147053119.1|1943926_1945300_+|insulinase-family-protein	gnl|CDD|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	1.41399e-54
NZ_CP042437.1|WP_147060917.1|1935335_1937072_-|DUF885-family-protein	gnl|CDD|377577	pfam05960, DUF885, Bacterial protein of unknown function (DUF885). This family consists of several hypothetical bacterial proteins several of which are putative membrane proteins.	7.52577e-101
NZ_CP042437.1|WP_147060919.1|1954843_1957246_-|DUF4982-domain-containing-protein	gnl|CDD|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	1.96785e-77
NZ_CP042437.1|WP_147053121.1|1946913_1948761_+|UbiD-family-decarboxylase	gnl|CDD|376697	pfam01977, UbiD, 3-octaprenyl-4-hydroxybenzoate carboxy-lyase. This family has been characterized as 3-octaprenyl-4- hydroxybenzoate carboxy-lyase enzymes. This enzyme catalyzes the third reaction in ubiquinone biosynthesis. For optimal activity the carboxy-lase was shown to require Mn2+.	2.3444e-131
NZ_CP042437.1|WP_147053114.1|1937208_1937697_+|DinB-family-protein	gnl|CDD|378981	pfam12867, DinB_2, DinB superfamily. The DinB family are an uncharacterized family of potential enzymes. The structure of these proteins is composed of a four helix bundle.	7.68037e-05
NZ_CP042437.1|WP_147053120.1|1945400_1946702_+|insulinase-family-protein	gnl|CDD|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	6.47428e-51

Protein sequences

>NZ_CP042437.1|WP_147053118.1|1942729_1943566_-|TSUP-family-transporter
MSVIVLTLIILIGSYFAGLLGSLTGLGGGVVIIPLLTLLLKVDIHYAIGASLVSVIATSSGSAAAYVKEGITNIRLGMFLEIATTAGAMVGALIAVYIPTHFIAILFGVILILSAIMSLKKKVESVNQEPSVLAEKLKLNSTYPTANGSVAYKVKNVGGGFFMMMFAGTISGLLGIGSGALKVLAMDTIMRIPFKVSTTTSNFMIGVTAAASAVVYLQRGYIDPGLSMPVAIGVLLGALSGSKILVHTSSSGWLRWVFAVVVTFLASQMIYNGFAGKI
>NZ_CP042437.1|WP_147053117.1|1942204_1942594_-|DUF1634-domain-containing-protein
MNDSKKFRDTDMQAIIGWILRAGVFISMSVVFIGGVVYLYRHGQTHVDYSTFKGVPDFVGSVGGILHGIFTGRGRAIIQAGIILLIATPIIRVVFSAIGFVMEKDYLYLGITILVLLIIMASMLSGHAG
>NZ_CP042437.1|WP_147060918.1|1941921_1942137_-|KTSC-domain-containing-protein
MQRQSVQSSALNSAGYDPSSKILELEFRDSGGVWQYFGFSNASFKKFMSAESLGKFFITQIKGKYPEIRIR
>NZ_CP042437.1|WP_147053116.1|1939368_1941807_+|TonB-dependent-receptor
MKVLFGGIFFAILTGVCYGSFAQTKSSVIQGKVLTEVNSPAEAATVVLMLAADSAIIKSTLADKSGLYQLTNIKPGNYILLASQIGSTKVYTGTFGLVAGQTFVAPTITLKQTNTQLKAVTVVARRPYIQVKPGKIVLNVQNSILADGNSAYEVLRQSPGVHVGGDKESLIISGRQPALITIDGRATNLTGDDLNNLLRSMQSSTIDQIEIISTASAKYDASGGGIINIVLKKGKNVGTNGTITAGAGYGKYAKGRAGIVFNNRSAKVNVFGNYSFDDNKTTRIINTDRNISYHDTLSDYNVAYHNIQKTQNHNFKAGLDYSLSSKQSIGFLVSGIITDSKFIKDNTLKISNQNKLDSIIISQSNLDRGSNFLNYNINYNAELDKSGKNLSADATYSTYSRHSNEFITNNFYTPGGINYRDAQQLENISPSSIHIWTFKADYVNPLTKTSRIEAGAKYNFAKSDNNLTFGPRVGNVYQADPNFSNRFLYIEKVSAGYINYINKVGKWDITTGLRAENTNSKGSSVSTAWVTTSYKYFNLFPQTQVSYTYNEKNVFGISYNRGIHRPDYQDINPFLYYTDPYDYRSGNKNLKPEYTDAVQLSHTYNDTFITTLYYNQTNDAYDFPVYRQNDTTKVNITERKNFGHIYVYGVSFYAPVQFTKWWSANFNLDASYLRYKAYPVNGSFNKASQDIIFNSTQTFAISSTIAAEITGRYESPTLYGVNQLKQSYTVNTGISKSIFNKRASIKINLNDIFNTDRDRNHAMYQNIDLSEYNKKETRVLRIGFSYRFGKMSVKSAAKHNTGSDDEQRRTGN
>NZ_CP042437.1|WP_147053115.1|1937773_1939090_-|DUF3887-domain-containing-protein
MKKVSFLVLMLCFAGRIFAQTEPANYKVALNRFIHLYNANQPDSIFNYFSPEMKAALPLESFKTTTLQLKAQMGSLDRTDFVKFASPIASYKATFSKGTYLLNIALNDKNQFTGLFLKPFEGVPADATAPAPASAATFVMDPSIQETPVTVKNLAGSISGTLAIPKNVTGKIPVVIIIAGSGPTNRDGNSPKLGLATNAYKMIANELGKSGIASLRYDKRLVGKSVSSTTEDQLRFEDYVEDGVNLINFLTDDERFSRIIILGHSEGSLVGMLSSIDQPVKGFISVAGAGDSADNILTEQMKSQPTHISEGFKRMLDSLKKGKTTDNIDPSLYFIARPGIQKYLMSWFRYDPTRAIKRLKIPILIVQGTTDLQVKVSNAEKLKKAKSDAVLEIIPEMNHVLKDAPADKDKNMATYNEPDLPLKPEFIKAVISFVKKVR
>NZ_CP042437.1|WP_147053114.1|1937208_1937697_+|DinB-family-protein
MNDNHNILVGEIVHLLQGGNAHADIKKALQNLPKTLRSAKPDKLPYSIWQLTEHIRIAQWDMLEFCKDGSHQSPKWPEGYWPKETGPESDEAWENSVQQIDRDLNELVSLVKTGDLFTKIPHGDGQNILREALQVADHTAYHVAEIIVIRRLLGAWRSPLTP
>NZ_CP042437.1|WP_147060917.1|1935335_1937072_-|DUF885-family-protein
MVALTGCKKDSASRGPNFAKDDAAFTIYENSFLENLWKLNPDWATTAGYHKYDSLLYIPNDQSRDKMLDFAKVQMDSLSRFDVNTLNEGNRIDYNMMQNQLDYAQWQIKQLKSYEWDPSSYNVIGTFAYILNEHYAPLPKRLHNFYQRMLNVPLFYKDAEKQIKNPVTELVSLAIEQNLGGVDVIGKDFADSLQKTNIPKAEQKLMVDRAAVTVKAIKDYAEWLKNLKNDHPRNFRLGRDLYEDKFKYEVVAAKTAQQVYNTAVQRKKYVHQQMAKISRQLWPKYFGKKVMPADSLEMISQMIDTLSGNHVKPDDFQSAIVQLIPKLNNFVRTKDLLTLDATKPLIIRKEPGYMAGVAGASMSGPGPYDKDGNSYYNVGSLSGWPKEKAESYLREYNQYIIQILSIHEAVPGHYVQGVYANKAPSIIKAVFGNGAMQEGWAVYAEEMMLNAGYGNNEPEMLLMWYKWNLRSVCNTILDYSVHSGSMTKEQAIKMLTTEAFQQQAEADGKWKRVSVSSVQLTSYYTGYKEITDLRDAYKEKMGDKYKLKEFNEKFLSYGSAPVKFIKDAMLAKPAAKKE
>NZ_CP042437.1|WP_158642863.1|1935022_1935277_+|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin
MAKEAYEWYEEQQAGLGDLFLKELDSCYDKIEIWPSAYAKVKKNFRQIILKKFPYIVVFEIFENDVVIYAIFHTSRSPRKKFIK
>NZ_CP042437.1|WP_147053112.1|1934747_1934987_+|hypothetical-protein
MTTLTMRQKLMSYLADADDSKVNALYKLLERDIQEEEVFTLSNEQLDILKKEREMHLSGQSKSYSRQEASQIIKGQQSF
>NZ_CP042437.1|WP_147053111.1|1934258_1934507_+|hypothetical-protein
MLQQIAFIPQHQFHVLINFKNDERAVAVLPNEAGKFRVVDQGKVIAEVNFDKNRSNVVCSRGKLGAYVMAQLANQIKNHYAS
>NZ_CP042437.1|WP_147053119.1|1943926_1945300_+|insulinase-family-protein
MNKKACLLTILSALLPALIFAQLKLPANMFLKKLPNGLDVLVVEDNSVPLATIMITTKNGSYTETPKFNGLSHLYEHMFFKANKDYKNQEDFLDRVSELGMQFNGSTTYENVNYYFTLPKFNLNQGLGFMNSAIRYPSFNAEEMARENIVVDGEFQRQESSPTYALSDAMDHHMWGDLYSRKNAIGNHDVIRTATPDLMDSIKNKYYYPNNSLLTVAGDVEHEDVFKKVEAIYGSWKPSKFDPFKKWPIPEFKPLAKPDYFIAESALSNVPLIMIDWQGPDTRNDVQSTYAADVFSYILNQNSSTLKKALVQSGLALDVSISYLTLSHVGPITLFIVPNPNKIKECMAEVKRQLELMDKDDYVTDEQITTSKQKLGILKIQEEEVASDFVQVLSFWWSSASLDYYTTYNTRLNQVTRADLQNYVRKYIKNRPYCAGMLINPELASQVNPKTFFNASN
>NZ_CP042437.1|WP_147053120.1|1945400_1946702_+|insulinase-family-protein
MKKILTAILFICGSLSVMAQSETTSFDVDGIKVIFKPTLKDIINVRMFYRGGVTNYPASQAGIEKFALEATTECGTKKYSGNVYRDRADVYGVDVASEGEYDYGNIQMQCITKYFNEGWDLFTESVVNPVFDAGEVELLRSKIVAKMREDQSNPDKRAEQLVLQSAFEGTPYATDPDGTEEILSKLTAADLKNYYSSIFNKNRMFIVVAGKISKEALIAKIKASFAGLPSAPYTPVALKEPAWNDYKVVKEDRNLQTNYIDAIMNGPAFNSPDYVAYRVGISALGGSLFSELRTKLNLSYDPGTYSVMQHMPYALMYVSTTSPKEAVTAMNQQLNKVLSYGLSPEGLKRIKSSFITSNYIKQQSTASITGSLGIAEILGGWQLAEDLPKAIENVTVAQINDAMQKYIVGLRWSYLGDLKKAEEADAAFKMLIH
>NZ_CP042437.1|WP_147053121.1|1946913_1948761_+|UbiD-family-decarboxylase
MGYKSLQACIADLEKHGHLVRIKEEVDPHLQMAAIHLRVFENQGPAILFENVKGSKFPAVSNLFGTLERSKFIFRDTLEKIKTLVELKNDPVKAVKNPFKYANVALTALSALPMKGSGSSAPVNFGKCTISDIPQIVNWPMDGGPFVTMPQVYTEDADKPGIMNANLGMYRIQLAGNDYILNKEIGLHYQLHRGIGVHQTKANAKGQPLKVSIFVGGPPSHPVAAVMPLPEGLSEMTFAGALGNRRFRYFYDDEGFCISSDADFVITGTVMPMENKPEGPFGDHLGYYSLAHDFPLLKVHNVYHRKAAIWSFTVVGRPPQEDTSFGALIHEISGAALPKEIPGLHAVNAVDAAGVHPLLFATGSERYTPYIKERKPQEILTIANHILGKSQLSLAKYLLIAAQEDDPNLDVNNIEGFLLHILQRVDFTRDLHFYTRTTIDTLDYSGDGLNTGSKVAITVAGDIKRELWTALPSWFDLPRPITNIKMAMPGVLMVEVPKHINHKDIDNVISIIEYRLKEEEDELGGLALMILCDDASFAAANINNFVWVTFTRSNPSHDIYGIGSFTEHKHWGCTGPLIIDARIKPHHAPVLERDPEVEKLVDKMGERGGALYGLI
>NZ_CP042437.1|WP_147053122.1|1948922_1949621_+|hypothetical-protein
MKNISIYILSVALLASACIKKDVAYYSISKVTKSDTASKVIVNIKARLTKDQLLGIAGKIKSDSAALPNLQLCYMLPGHNDKNTGSNNFYAIAKYPSAQTATMQDTLKDSEGNVVRLKITGVSAQMAQKLVNFHPKELKDQNFFGHFIDDNNHTVIIPFRDLTDPKKEYYILELDTTGKVVSATIPTVVTKDGIEKWFVTDRGDYITIKDSILTQYSIDDLGMPYNSIKSGL
>NZ_CP042437.1|WP_147053123.1|1949740_1951120_+|insulinase-family-protein
MTRNLIKTLTLSVIGVFSFCFAIAQPRLPEGYFWKKLPNGLEVVVIENSKVPLATIEIAVKNGAYTEGPEFSGLSHMFEHMFFKANKDYPDQASFLKRTQELGAIWNGTTDVERVNYFFTFDRDSLSAGLKFMNAAIRFPIYREEDMKKERPVVDGEFQRAESDPGFQLWYGIQQKLWGDLITRKNPIGIHEVINTATPEKMMVIKNKYYFPNNSLLTICGDVKHDAAFAMAEKIFGDWESSGFNPHEKYPIPAFKPLTKKEYFIKETTIAQTPSMQISWQGPSYLTDSASTVAADLFGTIVGLNSSKLQQALVDKGLASSVYVNYTTSKYVGPIDMGIEPNPTKLKECYDEVINQISLWAKDDYYTDEQLKDAKAILMRNSIHRKEKPSTLASQLSYQWCSTSLNFATDLDSNYQKVTRADIKKFVDTYIIGKPYAAGLIISPDLSKQLNAASFFVAK
>NZ_CP042437.1|WP_147053124.1|1951136_1952474_+|insulinase-family-protein
MMKKYMFALLIVAAIGNIKTVQAQKAAYETSVDGVKVIVQPSGNDIVEIQTIIKGGVQNYTAEKMGIESMAMNALTECGTVKHDKNAFKDILDKVSATVYGYSNKNYSVVRMNCIKSDLDVVWPLYVEAMTQPRFDAKEFARIKTDAITQLKSLDSRPDNAIDKFADKVAFVNRDYAKDPMGTVDILTKLTPEETKAYYSSIFTKSRLLIVVVADLDQATIEAKVKAMLDGVKKGPAFTFKKASFKVYKNSINVEQRDLATNYVEGITSGPIPGTEDFDAFNVAMRIFANRHFLDVRTNNGLSYAPQAWFSVGQTSTARFSVSTTQPDKYIAVFDKLVDKVKTEGFKPEEVANMKVTYLTGFYYKNETNSAQASSIASNEVLFDNWKRSLTLVDDVKKLTVEQVNNAFKTYINNIVWVYQGDPKKVNQILYINGTLNKGENGVSH
>NZ_CP042437.1|WP_147053125.1|1952651_1953749_-|AI-2E-family-transporter
MPAKEYPFFLKSTVIMFGLILLVYIFYQLADVFVPVAYSLFIAILLNPVCNWLESKKVPKALAISITLLLASIAIAGLFYFLSTQIIQFGDSLPVLKQKFATISASAQSWVATTFGYPIQKQNLLIKEAMNNSQSLLGSTLGSVLGIFGLIFIIPVYVFLVLYYKTLLLNFFYEVFSEENSKQVAEILKETKTAIQSYIIGLLIEMMIVAAMNSLALILLGVKYGILIGVIGAILNLVPYLGGIIAIALPVLMATVTKDGYATQLGVIVAYLVIQFIDNNILVPRIVSSKVQINALMSIIVVLLGNMLWGLSGMFLSIPFIAVLKIIFDRIDGLKPWGKLLGDTVPTRHKGEIWKRRKKVILPEQ
>NZ_CP042437.1|WP_147053126.1|1953916_1954363_+|hypothetical-protein
MNLDRYNYQISNDHQDYIFYSEGPKGKIKKIVRFSKIQDLESTVYNLGFGDADDETGVVDDSVVTNNKDSSMVLATVANTVIDFTNYYGNQYIYATGSTPARTRLYQIGIAGLWEKISIDFEVYGLKEDSWHEFKKNVNYDAFLVRRK
>NZ_CP042437.1|WP_158642864.1|1954397_1954562_+|hypothetical-protein
MPTTIKKATSKKSYSGDIINDDVKSYADEPYFVKKTEEARATLKRVGLPGQKKK
>NZ_CP042437.1|WP_147060919.1|1954843_1957246_-|DUF4982-domain-containing-protein
MKLSGLLLIALFFSAKTFAQQTRQTLDFDKGWRFNLGEVADAEKPATSDTKWRSLNLPHDWSVEGKFSKDNPATPEGGALPGGIGWYRKSFTVPASSKGKLVYIDFDGVYQKSKVWINGHLLGFRPNGYISFRYELTPYLNFGGNNVIAVKVDNSVQPNSRWYSGSGIYRNVWLVTTAKTAINHWGTFVTTTDVSNASAKVNIKVSVKNGAPSAALVVKTTLYDALGKAVAGGGAIPSKTQLQDTVFETSTTLAVKNPTLWSVDKPYLYKAVTQVLSGKTVIDEYTTPVGIRYFNFDLDKGFSLNGKAMKILGVCDHHDLGSLGAAINTRALERQLQILKAMGCNGIRTSHNPPAPELLDLCDKMGFIVMDEAFDCWEWEKVKYDYHLYFKEWHKRDLEDQVLRDRNHPSVMIWSIGNEIPQQHDTTALRIAPELSAIVHSLDTTRPITAANNNPDKNNKIISSGAIDLVGYNYHEGEYAAFHDRYPGKKFIATETTSGLETRGFYEMPSDSIRVWPEKWDKPFEREGNNVSAYDNVRPPWGSTHEMTWKVMKKYDFLSGMFIWTGFDYLGEPTPYSWPSRSSYFGIVDLAGFPKDVYYMYQSEWTNKPVLHIFPHWNWTPGKMVDVWAYYNSADEVELFLNGKSLGTKKKTGDDLHIMWRVKYEPGTLKAVSRKDGKVVLTKLIHTAGEPARIELSADRKLIKADGKDLSFITVKILDKDGNVVPDADNLVDFKISGPAFVASVDNGDPVTHDSFKVSYRKAFHGLALAIVQAKEKAGAVTFTATSKGLPAATITLNAK

Crispr_ID: NZ_CP042437_5

• CRISPR_ID: NZ_CP042437_5
• CRISPR_location: 2560763-2560855
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: cas3

Consensus repeat of NZ_CP042437_5

Consensus_repeat	Method
CGAAGCAATCCCCGATTTGCTAAGT	CRISPRCasFinder

spacers of NZ_CP042437_5

>5.1|2560788|43|NZ_CP042437|CRISPRCasFinder
TCCACCTATACTATCAATATCGAATATCCGTCATTGCGAGGTA

CRISPR arrays and Neighbor proteins around NZ_CP042437_5

CRISPR arrays

The CRISPR arrays of NZ_CP042437_5

>merge|NZ_CP042437|5|2560763-2560855|CRISPRCasFinder
CGAAGCAATCCCCGATTTGCTAAGTTCCACCTATACTATCAATATCGAATATCCGTCATTGCGAGGTACGAAGCAATCCTCGATTTGCTAAGT

>NZ_CP042437|5|5|2560763-2560855|CRISPRCasFinder
CGAAGCAATCCCCGATTTGCTAAGT	TCCACCTATACTATCAATATCGAATATCCGTCATTGCGAGGTA
CGAAGCAATCCTCGATTTGCTAAGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147053544.1|2557044_2558430_-|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|349879
NZ_CP042437.1|WP_147053548.1|2565259_2567092_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	unknown	unknown	gnl|CDD|369630
NZ_CP042437.1|WP_147053543.1|2554193_2555141_+|tryptophan-2,3-dioxygenase	unknown	unknown	gnl|CDD|226014
NZ_CP042437.1|WP_147053542.1|2553531_2553996_-|universal-stress-protein	unknown	unknown	gnl|CDD|366180
NZ_CP042437.1|WP_147053553.1|2571392_2574563_-|UvrD-helicase-domain-containing-protein	unknown	unknown	gnl|CDD|223288
NZ_CP042437.1|WP_147053538.1|2547708_2548890_-|formimidoylglutamase	unknown	unknown	gnl|CDD|212514
NZ_CP042437.1|WP_147060945.1|2555376_2556618_-|MFS-transporter	unknown	unknown	gnl|CDD|340863
NZ_CP042437.1|WP_147053540.1|2550068_2550596_+|hypothetical-protein	unknown	unknown	gnl|CDD|260119
NZ_CP042437.1|WP_147053541.1|2550687_2551674_+|acyltransferase-family-protein	unknown	unknown	gnl|CDD|224748
NZ_CP042437.1|WP_147053546.1|2561023_2561401_-|RidA-family-protein	unknown	unknown	gnl|CDD|129116
NZ_CP042437.1|WP_147053545.1|2558568_2560671_-|ATP-dependent-DNA-helicase-RecG	cas3	cd09639_cas3_CAS-I	gnl|CDD|236794
NZ_CP042437.1|WP_147053556.1|2575349_2577074_-|glycoside-hydrolase-family-3	unknown	unknown	gnl|CDD|366376
NZ_CP042437.1|WP_147053549.1|2567496_2568369_-|EamA-family-transporter	unknown	unknown	gnl|CDD|227339
NZ_CP042437.1|WP_147053554.1|2574703_2574937_+|hypothetical-protein	unknown	unknown	gnl|CDD|275028
NZ_CP042437.1|WP_147053555.1|2574943_2575243_+|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	unknown	unknown	unknown
NZ_CP042437.1|WP_147053547.1|2561920_2565241_+|SusC/RagA-family-TonB-linked-outer-membrane-protein	unknown	unknown	gnl|CDD|274948
NZ_CP042437.1|WP_147053539.1|2549089_2550055_+|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187539
NZ_CP042437.1|WP_090641689.1|2551943_2553233_+|HAD-IB-family-phosphatase	unknown	unknown	gnl|CDD|236985
NZ_CP042437.1|WP_147053551.1|2569013_2570357_-|M28-family-peptidase	unknown	unknown	gnl|CDD|349894
NZ_CP042437.1|WP_147053552.1|2570731_2571100_-|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP042437.1|WP_147053545.1|2558568_2560671_-|ATP-dependent-DNA-helicase-RecG	cas3	cd09639_cas3_CAS-I	7.9e-11	36.3	0.1

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147053544.1|2557044_2558430_-|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|349879	cd03883, M28_Pgcp_like, M28 Zn-Peptidase Plasma glutamate carboxypeptidase. Peptidase M28 family; Plasma glutamate carboxypeptidase (PGCP; blood plasma glutamate carboxypeptidase; EC 3.4.17.21) subfamily. PGCP is a 56kDa glutamate carboxypeptidase that is mainly produced in mammalian placenta and kidney, the majority of which is thought to be secreted into the bloodstream. Similar proteins are also found in other species, including bacteria. These proteins contain protease-associated (PA) domain inserts between the first and second strands of the central beta sheet in the protease-like domain. The PA domains may participate in substrate binding and/or promoting conformational changes, which influence the stability and accessibility of the site to substrate. The exact physiological substrates of PGCP are unknown, although this enzyme may play an important role in the hydrolysis of circulating peptides. Its closest homolog encodes an important brain glutamate carboxypeptidase II (NAALADase) identical to the prostate-specific membrane antigen (PSMA), which serves as a marker for prostatic cancer metastasis. Hypermethylation of PGCP gene has been associated with human bronchial epithelial (HBE) cell immortalization and lung cancer. PGCP also provides an attractive target for serological analysis in hepatitis C virus (HCV)-induced hepatocellular carcinoma (HCC) patients.	3.27014e-133
NZ_CP042437.1|WP_147053548.1|2565259_2567092_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	gnl|CDD|369630	pfam07980, SusD_RagB, SusD family. This domain is found in bacterial cell surface proteins such SusD and SusD-like proteins, as as well RagB, outer membrane surface receptor antigen. Bacteroidetes, one of the two dominant bacterial phyla in the human gut, are Gram-negative saccharolytic microorganisms that utilize a diverse array of glycans. Hence, they express starch-utilization system (Sus) for glycan uptake. SusD has 551 amino acids, and is almost entirely alpha-helical, with 22 alpha-helices, eight of which form 4 tetra-trico peptide repeats (TPRs: helix-turn-helix motifs involved in protein-protein interactions). The four TPRs pack together to create a right-handed super-helix. This is predicted to mediate the formation of SusD and SusC porin complex at the cell surface. The interaction between SusC and TPR1/TPR2 region of SusD is predicted to be of functional importance since it allows SusD to be in position for oligosaccharide capture from other Sus lipoproteins and delivery of these glycans to the SusC porin. The non-TPR containing portion of SusD is where starch binding occurs. The binding site is a shallow surface cavity located on top of TPR1. SusD homologs such as SusD-like proteins have a critical role in carbohydrate acquisition. Both SusD and its homologs, contain about 15-20 residues at the N-terminus that might be a flexible linker region, anchoring the protein to the membrane and the glycan-binding domain. Other homologs to SusD have been examined in Porphyromonas gingivalis such as RagB, an immunodominant outer-membrane surface receptor antigen. Structural characterization of RagB shows substantial similarity with Bacteroides thetaiotaomicron SusD (i.e alpha-helices and TPR regions). Based on this structural similarity, functional studies suggest that, RagB binding of glycans occurs at pockets on the molecular surface that are distinct from those of SusD.	2.04833e-41
NZ_CP042437.1|WP_147053543.1|2554193_2555141_+|tryptophan-2,3-dioxygenase	gnl|CDD|226014	COG3483, TDO2, Tryptophan 2,3-dioxygenase (vermilion) [Amino acid transport and metabolism].	7.8476e-27
NZ_CP042437.1|WP_147053542.1|2553531_2553996_-|universal-stress-protein	gnl|CDD|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	2.79318e-31
NZ_CP042437.1|WP_147053553.1|2571392_2574563_-|UvrD-helicase-domain-containing-protein	gnl|CDD|223288	COG0210, UvrD, Superfamily I DNA and RNA helicases [DNA replication, recombination, and repair].	6.33639e-98
NZ_CP042437.1|WP_147053538.1|2547708_2548890_-|formimidoylglutamase	gnl|CDD|212514	cd09988, Formimidoylglutamase, Formimidoylglutamase or HutE. Formimidoylglutamase (N-formimidoyl-L-glutamate formimidoylhydrolase; formiminoglutamase; N-formiminoglutamate hydrolase; N-formimino-L-glutamate formiminohydrolase; HutE; EC 3.5.3.8) is a metalloenzyme that catalyzes hydrolysis of N-formimidoyl-L-glutamate to L-glutamate and formamide. This enzyme is involved in histidine degradation, requiring Mn as a cofactor while glutathione may be required for maximal activity. In Pseudomonas PAO1, mutation studies show that histidine degradation proceeds via a 'four-step' pathway if the 'five-step' route is absent and vice versa; in the four-step pathway, formiminoglutaminase (HutE, EC 3.5.3.8) directly converts formiminoglutamate (FIGLU) to L-glutamate and formamide in a single step. Formiminoglutamase has traditionally also been referred to as HutG; however, formiminoglutamase is structurally and mechanistically unrelated to N-formyl-glutamate deformylase (also called HutG). Phylogenetic analysis has suggested that HutE was acquired by horizontal gene transfer from a Ralstonia-like ancestor.	6.14873e-99
NZ_CP042437.1|WP_147060945.1|2555376_2556618_-|MFS-transporter	gnl|CDD|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.90383e-54
NZ_CP042437.1|WP_147053540.1|2550068_2550596_+|hypothetical-protein	gnl|CDD|260119	cd13956, PT_UbiA, UbiA family of prenyltransferases (PTases). Many characterized members of the UbiA prenyltransferase family are aromatic prenyltransferases and play an important role in the biosynthesis of heme, chlorophyll, vitamin E, and vitamin K. They contain two copies of a motif similar to the active site DxxD motif of trans-prenyltransferases and are potentially related. Prenyltransferases (PTs) catalyze the regioselective transfer of prenyl moieties onto a wide variety of substrates and play an important role in many biosynthetic pathways.	0.00944186
NZ_CP042437.1|WP_147053541.1|2550687_2551674_+|acyltransferase-family-protein	gnl|CDD|224748	COG1835, COG1835, Predicted acyltransferases [Lipid metabolism].	6.52952e-24
NZ_CP042437.1|WP_147053546.1|2561023_2561401_-|RidA-family-protein	gnl|CDD|129116	TIGR00004, RutC_family_protein, reactive intermediate/imine deaminase. This protein was described initially as an inhibitor of protein synthesis intiation, then as an endoribonuclease active on single-stranded mRNA, endoribonuclease L-PSP. Members of this family, conserved in all domains of life and often with several members per bacterial genome, appear to catalyze a reaction that minimizes toxic by-products from reactions catalyzed by pyridoxal phosphate-dependent enzymes. [Cellular processes, Other].	6.10344e-62
NZ_CP042437.1|WP_147053545.1|2558568_2560671_-|ATP-dependent-DNA-helicase-RecG	gnl|CDD|236794	PRK10917, PRK10917, ATP-dependent DNA helicase RecG; Provisional.	0
NZ_CP042437.1|WP_147053556.1|2575349_2577074_-|glycoside-hydrolase-family-3	gnl|CDD|366376	pfam00933, Glyco_hydro_3, Glycosyl hydrolase family 3 N terminal domain.	3.7857e-75
NZ_CP042437.1|WP_147053549.1|2567496_2568369_-|EamA-family-transporter	gnl|CDD|227339	COG5006, rhtA, Threonine/homoserine efflux transporter [Amino acid transport and metabolism].	3.96623e-81
NZ_CP042437.1|WP_147053554.1|2574703_2574937_+|hypothetical-protein	gnl|CDD|275028	TIGR04172, putative_dgqhr_domain_containing_protein, DNA phosphorothioation-associated DGQHR protein 1. The DND system produces an phosphorothioation modification to DNA, replacing a non-bridging oxygen of a phosphate group with sulfur. The modification causes DNA degradation during electrophoresis in Tris buffer. This protein, like DndB (TIGR03233), contains a DGQHR domain (TIGR03187), which also occurs in several contexts that suggest lateral transfer rather than DNA phosphorothioation-dependent restriction.	0.00979238
NZ_CP042437.1|WP_147053547.1|2561920_2565241_+|SusC/RagA-family-TonB-linked-outer-membrane-protein	gnl|CDD|274948	TIGR04056, OMP_RagA_SusC, TonB-linked outer membrane protein, SusC/RagA family. This model describes a distinctive clade among the TonB-linked outer membrane proteins (OMP). Members of this family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 alone. Published descriptions of members of this family are available for RagA from Porphyromonas gingivalis, SusC from Bacteroides thetaiotaomicron, and OmpW from Bacteroides caccae. Members form pairs with members of the SusD/RagB family (pfam07980). Transporter complexes including these outer membrane proteins are likely to import large degradation products of proteins (e.g. RagA) or carbohydrates (e.g. SusC) as nutrients, rather than siderophores. [Transport and binding proteins, Unknown substrate].	0
NZ_CP042437.1|WP_147053539.1|2549089_2550055_+|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187539	cd05228, AR_FR_like_1_SDR_e, uncharacterized subgroup of aldehyde reductase and flavonoid reductase related proteins, extended (e) SDRs. This subgroup contains proteins of unknown function related to aldehyde reductase and flavonoid reductase of the extended SDR-type. Aldehyde reductase I (aka carbonyl reductase) is an NADP-binding SDR; it has an NADP-binding motif consensus that is slightly different from the canonical SDR form and lacks the Asn of the extended SDR active site tetrad. Aldehyde reductase I catalyzes the NADP-dependent reduction of ethyl 4-chloro-3-oxobutanoate to ethyl (R)-4-chloro-3-hydroxybutanoate. The related flavonoid reductases act in the NADP-dependent reduction of flavonoids, ketone-containing plant secondary metabolites. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.72923e-76
NZ_CP042437.1|WP_090641689.1|2551943_2553233_+|HAD-IB-family-phosphatase	gnl|CDD|236985	PRK11790, PRK11790, phosphoglycerate dehydrogenase.	1.23192e-39
NZ_CP042437.1|WP_147053551.1|2569013_2570357_-|M28-family-peptidase	gnl|CDD|349894	cd05642, M28_like, M28 Zn-peptidase-like; uncharacterized subfamily. Peptidase family M28 (also called aminopeptidase Y family), uncharacterized subfamily. The M28 family contains aminopeptidases as well as carboxypeptidases. They have co-catalytic zinc ions; each zinc ion is tetrahedrally co-ordinated, with three amino acid ligands plus activated water; one aspartate residue binds both metal ions.	2.92695e-159

Protein sequences

>NZ_CP042437.1|WP_147053545.1|2558568_2560671_-|ATP-dependent-DNA-helicase-RecG
MDPFQTPLTYLKGAGQTRAEVLKKELAIATFEDLLRHFPFRYIDRTKFYKVKDINPDLPYVQVLARVISKQIVGEKHTKRLVVQTRDDTGTLELVWFKGINWIDKTIVPGTVYIVFGKAGSFNGQAQMAHPEMEIYSPANMQRQGNATLQPVYNSTEKLKQFQLDSKGIQKLTATLLGLHAKDIKENLPLYIIQHFKLLGRADAYRNIHFPADANLLNEALHRLKFEELFLLQLKLLRNKMLHTQKFKGNIFGTVGHYFNDFYHHKLPFQLTTPQKRVLKEIRQDTQRGVQMNRLLQGDVGSGKTVVALMAMLIAVDNGFQTCIMAPTEILASQHYQTISTLVGDGFIEVALLTGSTKQKDRRVLHQKLESGEMKILIGTHALIEDKVQFKNLGFVIIDEQHRFGVEQRARLWRKNVVPPHILVMTATPIPRTLAMTLYGDLDVSVIDELPAGRKPIQTLHFFDNQRLRVFGFMKKEIALGRQIYIVYPLIKESEKLDLKNLEEGIEIISREFPLPEYKISIVHGKLKPADKEFEMQRFIKGQTQIMVATTVIEVGVNVPNASVMIIENAERFGLSQLHQLRGRVGRGAEQSYCILMSSHKLSHDGKIRLNTMVKTNNGFEISEIDLQLRGPGNLDGTQQSGVLDLKVANLATDQELLFKARKTVEQIFTKDPQLALPENQVLHHAFETKNAGLSWDKIS
>NZ_CP042437.1|WP_147053544.1|2557044_2558430_-|M20/M25/M40-family-metallo-hydrolase
MKKTFTLLCAAMLSATFVHAQQDSLMIRKIYDEALVNGKSYESLRYLCKNIGQRISGSANAQKAVEWSKKLMESYGFDKVYLQEVMVPHWVRGAKETAFIIDGKNRIPVPIAALGMTVATPKEGITANVIEVQSLKELETLGEAAIKGKIVFFNRPFDPRFIETGRAYGTAGDQRFMGPAAAAKYGAVGVIVRSLTESLDDYPHTGATLVDKDGKNIPAAAISTKAANKLSAMLKMRKFPAAKFYFKQSCQLLPDVLSYNVVGELTGTAHPNKFITVGGHLDSWDLAEGAHDDGTGVMQSAEVLRVLKAVGYHPKNSIRAVFFMNEENGDKGGIKYAELAAQNKEEHIAAIETDEGGFTPRGFSFSDVSKDFIAKVNSNWKALLEPYEVDQLTIGGAGADIEPMKKTVPGVVLIGFRPDSQRYFDVHHTPNDVFENVNKRELELGDAGMAALIYLIDQHGF
>NZ_CP042437.1|WP_147060945.1|2555376_2556618_-|MFS-transporter
MRFCFTFAYSMQAVVIGFYMYQITHSAFALGLIGLCEAIPAISIALYGGYIADKSEKRKMLLLIFSGVILTSLVMFTVTLKSMSGIIHVGWIIPIIYVMIFCNGIARAFYGPATFTIYAHSIPKEVYPNGSTWSSSSWQVASIIGPAAGGLIYGYSDKFFGISGITATFGCIIFFLVVSLVLVALLRKYPPVFVPKENIWKSLSAGIEFVFGNKMMIGAMSLDLFSVFFGGAVALLPVFANEILKVGAEGLGIMRATSSLGAVLTMLVMTRFSPMGKPWRNLLIAVTGFGLSIICFGLSKSFYLSLFFIFTEGAFDSVSVIIRGTIMQLLTPDHMRGRVSAVNQMFIGSSNEIGAFESGTAARLMGTVPSVLFGGSMTMLIVGITYLKTKRLVPLSLSQIQPPEVAEEEIIAK
>NZ_CP042437.1|WP_147053543.1|2554193_2555141_+|tryptophan-2,3-dioxygenase
MQFSPEIEGRLAQLQEKYEAMGQDMNSYLDGLLYADFLTYWDYIHLDTLLSLQSPKTPFPDEEIFIIYHQITELYFKLALHECQQIAAAQPLTVDFFTARLKRINRYFGALTQSFEIMVDGMEKEQFLKFRMSLLPASGFQSGQYRMIEIYATDFINLVAKDKREELRTATIDEQFEYLYWKFGATELSTGKKTLTLKQFEKKYAKTFIELGKANVGYNFNTLALKFEAEGRLTPELKAELRQLDVNVNVNWPLSHYKSAVRYLNREPEEIKATGGTNWQKYLPPRFQKRIFYPSLWSADEVENWGKAWVDSVLG
>NZ_CP042437.1|WP_147053542.1|2553531_2553996_-|universal-stress-protein
MKISKILIGIDDSTYAHNAAAYGFDIAHTYNAAVGLVHIIEPTVFPQTPNDSLIGMPETMGIDQVELIDIQSKQSLSVIESIKKEYAGELEVTSFTDFNITADGILSCAKEFNADLIVLGTHSRTGLDRFLMGSVAENVVRHSTIPVLVVPFIA
>NZ_CP042437.1|WP_090641689.1|2551943_2553233_+|HAD-IB-family-phosphatase
MEQYFIIDFDSTFTQVEALDELARISLKNHPDREGIYKQIEDLTNASMEGRLSFTQSLEARVKLLCANRDHLKQLISHLKKKVSTSFSRNTIFFKNHQDEVLIVSGGFKEFITPVVTEYHIKKENIYANTFEFDDEGNIIGYDRTNPLSQEGGKVKLLKELQLPGDIYGIGDGYSDFQLKESGMIKKFYAFTENIERKSVTEKADHVTPSFDEFLYLNKLPRAISYPKNRIKCLVVGAIDEEAQAQMKKEGYNIRNRDEIEDKYLEEAGVLFCDEDHQPTPEQVQNSGRLKVIGIFGKCNNKLAETATENGIIIFDDPRHNPHNSDFLPKRVLAFMNEGKTHTSCNFPDLQPPRVNNAHRLIHIHKNVPGILAKINDVFARHNINIVGEFLVTNPQIGYVITDVNTGYDTQVLNELKAIEHTIKFRLLY
>NZ_CP042437.1|WP_147053541.1|2550687_2551674_+|acyltransferase-family-protein
MQPDKRNHLIDLLRILAASWVVFFHLNQPIKPIDNWYRDFCKYGHLGVPIFFIISGYCILIALHHAKKPTEFMVRRFFRIFPPYWFSLVTTAVIVLLLKVITHVNSVAVLPKSIAGILATITLTTTPITDIKTINWVYWTLSYEVFFYLAVFACAFFKKQYFVIALTGVTLLSIVLPRFESGPLFFLNLWPLFSLGVAIYQLLHQPAYKWFNIALLAFSAVDFYATHQSYIYIVLCLITGGLIVINHFKPLKSNLLSRYGDISYSLYLVHVPIGIYLLGHLKTTAIQTNVTLNILFDVVILIFLVFLSRLMHRYIELPAIKYGKRFGK
>NZ_CP042437.1|WP_147053540.1|2550068_2550596_+|hypothetical-protein
MDTEKRYTFNPRRLIFESVFTLALVGFAVWFTIKAVLLFPATGPLLLFLLFFFTGLISILYQQIKTWLVLRQYYQFDKDKTIILSADRLTLNMGKDNLDIHINSDEVVTVEIYEGKPWGRFQNFDYIILYTIDNQKVIITQFTVPLLVHDKVFKKFLRRKPRKYFKKRFNFIDVN
>NZ_CP042437.1|WP_147053539.1|2549089_2550055_+|NAD-dependent-epimerase/dehydratase-family-protein
MILITGATGFLGAELAKLLVTSGSNIRCTKRATSGIPALLAPFQSQIEWVEADMLDIFALENALVGVTQVYHCAAWVSLKSADKKPMINTNVTGTANLVNLCAEKGIRMVHVSSIAAIGLAKPGDLTTENHHLEQSTENDGYAISKLESEMEVWRGIAEGLDAVIVNPSLIIGASAGKVGSGALFETIRKGLKFYTAGTIGFVDVHDVAKCMVGLMNSDITAERYIISAENRTYQSITTEAANGFGIKPPAILAKPWLMEIGWRGAAVIAALTGGNPAIDKTSAQAASVTREFDNSKIRNAIGIEFKPINKTIKEICEALH
>NZ_CP042437.1|WP_147053538.1|2547708_2548890_-|formimidoylglutamase
MSLADFFKPIDLKKITPKKGYYTSQLGDKIVHYSVDFPDLEEKTDLAIIGVMDDRNATDNQGCALGPDYIREKLYQLNEGGYNLKIADLGNITAGASVTDTYFALKTVVSELVKKDIIPIILGGGQDLTYAQYLGYEDLEQKVDLVVVDARFDLDEDETPAGLETTSQSYLNKIFLHEPNYLFNFSNLGYQTYFASQESLRVMDKLYFDVHRLGELTGNIAVTEPAIRNASMVSFDVGSIRSADAAGNANATPNGFNGQEACQLCRYAGFNDKLSSIGFYEFNPAYDNNGQTAMLLAQMIWYFIDGFYGRKRDFPLNPKSQYLIYKTSLKHEDQEVVFVKSKKSDRWWMQVPYPTGGSKNERFHLVPCSYADYKTATSGELPDLWWRTYQKLN
>NZ_CP042437.1|WP_147053546.1|2561023_2561401_-|RidA-family-protein
MMEIINTNNAPAPIGPYSQATVAGNFVFVSGQIPLNPATGELVTSGIKDEAVLVMENIKAILTEAGIGFANVVKTSIFLTDLGNFGQVNEVYGTYFTSSFPARETVQVSALPKGVNVEISVIAVK
>NZ_CP042437.1|WP_147053547.1|2561920_2565241_+|SusC/RagA-family-TonB-linked-outer-membrane-protein
MNVFYQTKHRILRLFAVLLLIACAATASAQNKAVTGKIIDASTGEAVIGATVLAVGTSNGVAADLNGTFKITVAANTSLQFKSIGYTSVTVAADFDKPMIIKLTPSNKGLEEVVVVGYGQQKRATVSGAVATVSSKVFQDRGPINNPLESLQGQVPGVVVTRTSAQPGRENWNFQIRGATSTNTQDPLIVLDGVALVNNAELNSINPNDIDNISFLKDAAASIYGARAAFGVVLITTKKAKSGKMDVQYLSTISQKRLGLQPILINDRQWGQSLKEALTNDNYGVAPTNYLWYQLADLATHPPDSLYIDITRLPGYAGSANGVLYNGTPLPSFGDVKDFTFFDTNMQKMLWGNATSTQQDLSFSGSGDRSGYRVSLGYLNDGSQLKWGLNGNQRYNLRLNHSYKFSDRVNLETNISLERNNIQQPTLYSYGGYSALSNYAQPGLPAFTSKGQPYAWGTVYSAPALLKYGGDNKESNSRALLNSTFTYNFAKHLTFTAVTGYHVWYQDSRIQQKQVQFYNYAGNLLIQTNPINGGNGGSNTFYNRSNITEPYYNLAGRVSYDNVFNKIHAVGVMLGSSYERDEYNYFTTRTYNLGSDDIPSLGTGVTSGTAGFVTNGETQNHYALGSYFGRATYTYNSKYNLEVQGRYDGSSKFIADKRWKIFGSVLGSWLISEESFVKNLNIFSTLKLRASYGTTGSQSGIGLYDYLQSLNVNTGGALLGNNLATSVTTTGSLVSLNRTWETVVKKNLALDFAILNDHLSGSFDIYRNENNNMLLNQLYPGVLGASAPTQNIGTLHTWGYEGSLTWRSNIGKLTYSVSGTITDNQNKLVHFGGANVIAPGYNATVEGYPLGSYFGLKYGGKLQTQAEVDAYNAQYAPAGSTNNIGLPIPSALANPAGQMSGLRPGDNKFVDVNGDGKLSIGGTTADKGDLVYLGSDNPRYSYGLNLGLQWNGFDFYSIFQGVGKRAVLRTGSSANFSVPFLSIFQGQTTSYLGNVWSPENPDAYYPNLHSAQNNGINNYNYQPSTWRVQNGAYVRLKNVVLGYTIPKSLLAHTHAIKGLRIYFSGSDLWEKTYIHDGWDPEVTRTVSGNERYPFYRYLTLGANVTF
>NZ_CP042437.1|WP_147053548.1|2565259_2567092_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein
MKTKYIKFMSVIGFAFGFTIMSCNKALNLKPLDQLSDAAYFKSPTDFKTFANQYYGYLKNFTTINGLSDNPHSDGRSDLFGGGGAYGSGTNIVPVTEPGFGNAGNWTVDYGRIRAANYLLDKAASYPRPAEIAQYVAEAKFFRAYTYFDLLQQYGGVPLITKPLDLTSPELFGARATRDQVADLIIADLQAAIPALPVSLSTNSADFGRVTQMAAQAFLSRVALYEGTWQKFRSGDAARYNALLDKSIAASAAVMASNQYALFGTAASNALGGNSTVLGDSCLKYLFILENIKSNPAGITKTANHEYILSTRYDDVLKPANVFVSRSTMATGVAQKFVNMFLCTDGLPVEKSPQFGGFQTYLSEFQNRDNRLKYTIKITYQYYWYSINGRVNWTGDAADRANSLGPAKPYGYGNQKWISERQLVDGKESEDYPVIRYAEVLLNYAEAVYERNGIISDADLNKSVNLVRLRCNSTNGMPGLSNALVNTNNMDMRTEIRRERTIELYDEDFRFDDIKRWHSGTTDLVTNVGGTAYGNAAAFVSPWPVLYKYTGTQAELGPDPVKPVPTNAKDANGNLILDQTARLFGEKNYLYPLPSQQITLNPQLTQNPGW
>NZ_CP042437.1|WP_147053549.1|2567496_2568369_-|EamA-family-transporter
MQKNKIPIRPLLAVLGSILSVQIGAAIAKGLFPALGASVTATLRIGLSALMLLAVNRPGLKTLTKVQWRAVIPYGLCLGAMNLIYYLALSRIPLGIAVTLEFMGPLLLVVFSSKRLIEFLWVLLAAAGIALMTPWNNTNIDLFGAGMALLAGAFWAGYIVLGRRVSAVLNGGEAVTIGMLFALIITLPFAFASGGMLNFNSSMIIPAVGLALFCSAVPFSLEMYGLKYIPTKTFSILMSMEPAVGAICGLIFLKEYLSVQEYAAVVLVVIASVGATIGNRENIGKIAPDV
>NZ_CP042437.1|WP_147053551.1|2569013_2570357_-|M28-family-peptidase
MKYITILLLFVTTITSAQTIIKQDAQIKQMVDEVSSKNIEATIRKLVSFKSRHTLSDTTGKTTGSGAARNWIKGEMEKYASESGGRMTVAFDTFTQPKGTRIDKPVKLKNVLAILKGTDPTDTRVYLVSGHYDSRINDVMDANGVEPGANDDASGTALSMELARVMAKRSFPATIIFMTVVGEEQGLYGSTNVAKRAKAENWNVDAMLNNDIVGNTHGMETDLKDNRSVRVFSDGIPTNATDKQVAALKSLGGENDSPSRELARYAKETGERYVDQLDVKLIYRRDRYLRGGDHLPFLEQGFTAVRFTEMNEDFNRQHQNIRTENGVDYGDLPDFVDFNYVQKVARMNLSVLANLALAPARPQNVGIVTSDLTNKTKLTWEAPSAGKKPAGYYVLMRETTSAFWERKFYVADTTATLAYSKDNYFFAVQSVDADGHESLPVFPKPIR
>NZ_CP042437.1|WP_147053552.1|2570731_2571100_-|hypothetical-protein
MEDKYQKKYRISSPRLAGWDYGSHGLYFVTICTKHRIHYLGEVIQPENRSDAFVEYTDIGKIAHDNWLKITEFHPFVKLDDFCIMPDHMHAILFIDKPDKTSWEVNKLWRTKRKFGGSFTRV
>NZ_CP042437.1|WP_147053553.1|2571392_2574563_-|UvrD-helicase-domain-containing-protein
MQSNFNKYNDKFQSALAGLNPEQLAAVNKMDGPVLVVAGPGTGKTQILAARIGKILTDTDALPSEILCLTYTDAGAVAMRKRLFEFIGPDAYRINIYTFHAFCNEIIQENLEYFGKLNLESLSDLESAMLFRELVDEFANDHLLKRFTGDVYYDTKRLKDLFSTMKRENWDAAMIEKAVQEYLDDIPNREEFVYKRANSKTGIKVGDPKQKDIDAAHDLMKKLVAAVREYQNYDVKMKAKGRYDYDDMIIWVLRAFRDNDEILRKYQERYQYILVDEFQDTSGSQNELLRFLLNYWDVPNVFVVGDDDQSIFKFQGANMSNILDFASDYVSTLKTVVLKHNYRSNQHILDISKALIDNNQERLTKQLKLDKDLQASHARFTEMAVEPVIREYENPDQELVDVSAQIKKLIDKGAEPGEIAVIYRNHSQVEEMIQYLEVKKIAVNTRRKIDILTQPFGEKIINIMRYLMQELDSPYSGDELLFEILHYDFFNIAPIEIAKASIAVSQENFAANSRDKVKTSIRRYISELRPPAQPDLFAPDKYMEMRYLMNNIDDLLKSAVNSTLQAFFQDVIAKMGILKYIMQQPDKGGYMQMLTSFFDFLKDESRKNPDIKLSDLIATIELMKKNGIRLDLNKVIFSDNGVNFLTAHGSKGLEFEHVFFIGCDKRTWDSKGRNSGFSLPDTLTRSAADDIAQKEEARRLFYVAVTRAKQCLMISYAGKDKKGKDQEASQFIGEILASTDTQLQYPKVPADTMVDFIATQFSEVEKPKVELLDKNYINQLLQSYTLSVTHLNNYLDCPLRFYFQCLIRVPSGKSPSATFGQAVHWALNKTYRLLKENQDEFLSTEQFMNEFKWYMARNRDSFTKDEYKLRLAYGEKILPPYYEQNVGGWNKIAVTEKSIKNIEINGVPIKGNLDKMEFDGKNVTVVDYKTGKVRNAKDKLLRPTFDAPMGGDYWRQGVFYKILVDHDRTNDWEVIDTIFDFVEPVSEGEYYKEKYVISPADIELVTEQITDTYAKIMAHEFSTGCGKKECDWCHFVKTNFKQAEVVLNAVSEEEEG
>NZ_CP042437.1|WP_147053554.1|2574703_2574937_+|hypothetical-protein
MRTSQIRKQLHEYIETAEDDKLKAIYTLLQNEISDGYELTKAQREELDKRFSDHQNGLGQSFTWDETLTMAKQSLIK
>NZ_CP042437.1|WP_147053555.1|2574943_2575243_+|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin
MSYDLKIRQEATKEFSNAFLWYEEQQSGLGDVFETAIRRKLNQISRSPYHYKADYNQFHQALTEKFPFLIVYVIDENLKQITVMAIFHTSRNPNKKIRK
>NZ_CP042437.1|WP_147053556.1|2575349_2577074_-|glycoside-hydrolase-family-3
MPKLKTSYCFAFIISLNFIVINAFAQKESYIQSLNTQNHWVDSVYHKLSRKHRIAQLLFVRAHTNKGQAYADSVGKVIKDQQIGGLVFFQGGPGRQLNLVNQYQKLAKVPLLIAMDGEWGLGMRLDSTVSYPYQMTLGAIQDNTLIYKMGRQVAADFKRIGAHFNLAPDMDVNNNPNNPVINYRSFGDNKYNVAKKGIAYFTGMQDAGLLTAAKHFPGHGDTNVDSHFDLPLLPYSRARLDSLEEYPFREAIAAGISGVMIAHMSIPALDTTTHLPSTLSRPIITGILKDSLKFKGLVVSDAMEMKGVVKYFPNGDADVKAFVAGMDVIELSENSDRAINLIRKALRHGAISKAEFEIKVKKVLAAKYWAGLNQYREASPLNLNADINSPAQKDLVQQLSDAAVTILKGDASTIKLNPFLKTAIVSIGVSSPTAFQQEAAKSFPNCKLFMVDKNTPAIGLKNILSLLSQYQQVIVGVHDTRLRPQSKLDYNSDVKLMIADLAGRPNTVISVFANAYTIAGLPGIEKSKALMVCYQNSPELQKSVVKVLMGTLKPTGKLPVSVNVFFPTGTGIGL

Crispr_ID: NZ_CP042437_6

• CRISPR_ID: NZ_CP042437_6
• CRISPR_location: 2917819-2917954
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_6

Consensus_repeat	Method
CAAAAGTCTCCCCTACCGGGGGAGATTTAGAGGGGGCTT	CRISPRCasFinder

spacers of NZ_CP042437_6

>6.1|2917858|58|NZ_CP042437|CRISPRCasFinder
CTGGCCGGATAGTGTGTTTAGGTAGCTATTATATGTTGGATTCAGTCATTACTGAAGC

CRISPR arrays and Neighbor proteins around NZ_CP042437_6

CRISPR arrays

The CRISPR arrays of NZ_CP042437_6

>merge|NZ_CP042437|6|2917819-2917954|CRISPRCasFinder
CAAAAGTCTCCCCTACCGGGGGAGATTTAGAGGGGGCTTCTGGCCGGATAGTGTGTTTAGGTAGCTATTATATGTTGGATTCAGTCATTACTGAAGCCAAAAGTCTCCCCTACCGGGGGAGATTTAGAGGGGGCTT

>NZ_CP042437|6|6|2917819-2917954|CRISPRCasFinder
CAAAAGTCTCCCCTACCGGGGGAGATTTAGAGGGGGCTT	CTGGCCGGATAGTGTGTTTAGGTAGCTATTATATGTTGGATTCAGTCATTACTGAAGC
CAAAAGTCTCCCCTACCGGGGGAGATTTAGAGGGGGCTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147053837.1|2926714_2927497_+|indole-3-glycerol-phosphate-synthase-TrpC	unknown	unknown	gnl|CDD|234710
NZ_CP042437.1|WP_147053838.1|2927888_2929355_-|SusD/RagB-family-nutrient-binding-outer-membrane-lipoprotein	unknown	unknown	gnl|CDD|378943
NZ_CP042437.1|WP_147053827.1|2914319_2914613_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	unknown	unknown	gnl|CDD|368240
NZ_CP042437.1|WP_147053836.1|2925887_2926505_+|C26-family-cysteine-hydrolase-domain-containing-family	unknown	unknown	gnl|CDD|223586
NZ_CP042437.1|WP_147053822.1|2910722_2911019_-|hypothetical-protein	unknown	unknown	gnl|CDD|223619
NZ_CP042437.1|WP_147060957.1|2915268_2917701_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP042437.1|WP_147053830.1|2918748_2919834_+|acyl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173848
NZ_CP042437.1|WP_158642888.1|2911278_2911758_-|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|223619
NZ_CP042437.1|WP_147053833.1|2922881_2923670_+|hypothetical-protein	unknown	unknown	gnl|CDD|226720
NZ_CP042437.1|WP_147053820.1|2908699_2909206_-|DUF4440-domain-containing-protein	unknown	unknown	gnl|CDD|379639
NZ_CP042437.1|WP_147053821.1|2909307_2910603_-|amidohydrolase	unknown	unknown	gnl|CDD|349917
NZ_CP042437.1|WP_147053825.1|2911939_2912419_-|hypothetical-protein	unknown	unknown	gnl|CDD|223619
NZ_CP042437.1|WP_147053828.1|2914597_2914837_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053834.1|2923740_2924169_+|cytochrome-B	unknown	unknown	unknown
NZ_CP042437.1|WP_147053829.1|2917978_2918617_+|nicotinamide-mononucleotide-transporter	unknown	unknown	gnl|CDD|377432
NZ_CP042437.1|WP_147053835.1|2924403_2925813_+|anthranilate-synthase-component-I-family-protein	unknown	unknown	gnl|CDD|223225
NZ_CP042437.1|WP_147053826.1|2912481_2914227_-|aspartate--tRNA-ligase	unknown	unknown	gnl|CDD|234775
NZ_CP042437.1|WP_147053832.1|2922023_2922647_+|thiamine-phosphate-synthase	unknown	unknown	gnl|CDD|238317
NZ_CP042437.1|WP_147053831.1|2920080_2921799_+|alkaline-phosphatase-family-protein	unknown	unknown	gnl|CDD|293740
NZ_CP042437.1|WP_147053823.1|2910952_2911180_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147053837.1|2926714_2927497_+|indole-3-glycerol-phosphate-synthase-TrpC	gnl|CDD|234710	PRK00278, trpC, indole-3-glycerol phosphate synthase TrpC.	3.80347e-109
NZ_CP042437.1|WP_147053838.1|2927888_2929355_-|SusD/RagB-family-nutrient-binding-outer-membrane-lipoprotein	gnl|CDD|378943	pfam12771, SusD-like_2, Starch-binding associating with outer membrane. SusD is a secreted starch-binding protein with an N-terminal lipid tail that allows it to associate with the outer membrane.	2.66267e-144
NZ_CP042437.1|WP_147053827.1|2914319_2914613_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	gnl|CDD|368240	pfam05016, ParE_toxin, ParE toxin of type II toxin-antitoxin system, parDE. ParE is the toxin family of a type II toxin-antitoxin family. It is toxic towards DNA gyrase, but is neutralized by the antitoxin ParD. The family also encompasses RelE/ParE described in.	9.86712e-05
NZ_CP042437.1|WP_147053836.1|2925887_2926505_+|C26-family-cysteine-hydrolase-domain-containing-family	gnl|CDD|223586	COG0512, PabA, Anthranilate/para-aminobenzoate synthases component II [Amino acid transport and metabolism / Coenzyme metabolism].	8.47393e-92
NZ_CP042437.1|WP_147053829.1|2917978_2918617_+|nicotinamide-mononucleotide-transporter	gnl|CDD|377432	pfam04973, NMN_transporter, Nicotinamide mononucleotide transporter. Members of this family are integral membrane proteins that are involved in transport of nicotinamide mononucleotide.	5.17444e-46
NZ_CP042437.1|WP_147060957.1|2915268_2917701_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	4.89454e-28
NZ_CP042437.1|WP_147053830.1|2918748_2919834_+|acyl-CoA-dehydrogenase	gnl|CDD|173848	cd01159, NcnH, Naphthocyclinone hydroxylase. Naphthocyclinone is an aromatic polyketide and an antibiotic, which is active against Gram-positive bacteria. Polyketides are secondary metabolites, which have important biological functions such as antitumor, immunosupressive or antibiotic activities. NcnH is a hydroxylase involved in the biosynthesis of naphthocyclinone and possibly other polyketides.	2.80757e-52
NZ_CP042437.1|WP_158642888.1|2911278_2911758_-|peptidylprolyl-isomerase	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	4.81278e-22
NZ_CP042437.1|WP_147053833.1|2922881_2923670_+|hypothetical-protein	gnl|CDD|226720	COG4270, COG4270, Predicted membrane protein [Function unknown].	0.00339736
NZ_CP042437.1|WP_147053835.1|2924403_2925813_+|anthranilate-synthase-component-I-family-protein	gnl|CDD|223225	COG0147, TrpE, Anthranilate/para-aminobenzoate synthases component I [Amino acid transport and metabolism / Coenzyme metabolism].	3.66672e-140
NZ_CP042437.1|WP_147053820.1|2908699_2909206_-|DUF4440-domain-containing-protein	gnl|CDD|379639	pfam14534, DUF4440, Domain of unknown function (DUF4440).	5.93619e-05
NZ_CP042437.1|WP_147053821.1|2909307_2910603_-|amidohydrolase	gnl|CDD|349917	cd05667, M20_Acy1-like, M20 Peptidase aminoacylase 1 subfamily. Peptidase M20 family, uncharacterized subfamily of bacterial proteins that have been predicted as N-acyl-L-amino acid amidohydrolase (amaA), thermostable carboxypeptidase (cpsA-1, cpsA-2 in Sulfolobus solfataricus) and abgB (aminobenzoyl-glutamate utilization protein B), and generally are involved in the urea cycle and metabolism of amino groups. Aminoacylases 1 (ACY1s) comprise a class of zinc binding homodimeric enzymes involved in the hydrolysis of N-acetylated proteins. N-terminal acetylation of proteins is a widespread and is a highly conserved process that is involved in the protection and stability of proteins. Several types of aminoacylases can be distinguished on the basis of substrate specificity. ACY1 breaks down cytosolic aliphatic N-acyl-alpha-amino acids (except L-aspartate), especially N-acetyl-methionine and acetyl-glutamate into L-amino acids and an acyl group. However, ACY1 can also catalyze the reverse reaction, the synthesis of acetylated amino acids. ACY1 may also play a role in xenobiotic bioactivation as well as the inter-organ processing of amino acid-conjugated xenobiotic derivatives (S-substituted-N-acetyl-L-cysteine).	0
NZ_CP042437.1|WP_147053825.1|2911939_2912419_-|hypothetical-protein	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	3.43086e-29
NZ_CP042437.1|WP_147053822.1|2910722_2911019_-|hypothetical-protein	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	1.06847e-30
NZ_CP042437.1|WP_147053826.1|2912481_2914227_-|aspartate--tRNA-ligase	gnl|CDD|234775	PRK00476, aspS, aspartyl-tRNA synthetase; Validated.	0
NZ_CP042437.1|WP_147053832.1|2922023_2922647_+|thiamine-phosphate-synthase	gnl|CDD|238317	cd00564, TMP_TenI, Thiamine monophosphate synthase (TMP synthase)/TenI. TMP synthase catalyzes an important step in the thiamine biosynthesis pathway, the substitution of the pyrophosphate of 2-methyl-4-amino-5- hydroxymethylpyrimidine pyrophosphate by 4-methyl-5- (beta-hydroxyethyl) thiazole phosphate to yield thiamine phosphate. TenI is a enzymatically inactive regulatory protein involved in the regulation of several extracellular enzymes. This superfamily also contains other enzymatically inactive proteins with unknown functions.	2.76738e-45
NZ_CP042437.1|WP_147053831.1|2920080_2921799_+|alkaline-phosphatase-family-protein	gnl|CDD|293740	cd16016, AP-SPAP, SPAP is a subclass of alkaline phosphatase (AP). Alkaline phosphatases are non-specific phosphomonoesterases that catalyze the hydrolysis reaction via a phosphoseryl intermediate to produce inorganic phosphate and the corresponding alcohol, optimally at high pH. Alkaline phosphatase exists as a dimer, each monomer binding 2 zinc atoms and one magnesium atom, which are essential for enzymatic activity. Although SPAP is a subclass of alkaline phosphatase, SPAP has many differences from other APs: 1) the catalytic residue is a threonine instead of serine, 2) there is no binding pocket for the third metal ion, and 3) the arginine residue forming bidentate hydrogen bonding is deleted in SPAP. A lysine and an asparagine residue, recruited together for the first time into the active site, bind the substrate phosphoryl group in a manner not observed before in any other AP.	5.41543e-127

Protein sequences

>NZ_CP042437.1|WP_147060957.1|2915268_2917701_+|TonB-dependent-receptor
MALLLPVLASAQLSISGKVTNQSGEALPGATITINNPAASVVADATGKYGFTNLKPGSYTLNASFIGYQTISKNIVLAANQVINLALVNGTLAAEEVTISATRAVKNSPTAFTNLSKKDLAKNNFGQDLPYLLSLTPSVVTTSDAGAGIGYTGIRIRGSDNTRVNVTINGIPLNDAESQGSYFIDLPDLASSVDNIQVQRGVGTSTNGAGAFGGSINIQTTTRRDTAYAEINTSAGSYGSIKNTVNAGTGLLDGHFSLDGRLSRIHSNGYIDRATSDLKSLYLSAAWYGKNSTIRANVISGHERTYQAWNGIADYVIGDNTRKDNRTYNELGLMDDAGNFYKDQVDDYLQNHYQLLYDQKISSKLSFSGALHYTKGKGYYEEYRRQDAVANYGLTPVIMGMDTIKTTDLVRRLWLDNEFYGVTYALKYQPQSNLNMTLGGAYNEYKGAHYGNIIYTKESAGIGPNYEYYRDNAKKNDFNIFYRAEWHLNKVLLYADAQYRHLYYNFYGIDKNQQNAQQSIELNFFNPKVGITYQLNEQNNVYASFAVGNHEPNRDDYVNSTPQARPKAENLKDFEAGYRTVGKIFSGGINGFYMLYKNQLILTGALNDVGGAIRTNVPDSYRTGVELDGKVRITSQLNWGITATWSANKIKNYHQFFSNYDDGTLVEESFKKTTIAYSPSLTGASIISYSPVKGGEIAFISKYVGKQYLDNTMNQNPAGFNIAPDNQSNPYAANRYLKSYFTSDVRLRYNFSISQVKNIGLGLQVNNVFSKKYEANGATYPDIEGGNMVNYNYYFPQAPRNFMAMLSLNF
>NZ_CP042437.1|WP_147053828.1|2914597_2914837_-|hypothetical-protein
MLTDIEIKEKLIATISNTDNMELLRELLMITEMEDEISGVYQLSPEEIIAVNEGIEQIEKGMFVTNEEANKLIDKCLGR
>NZ_CP042437.1|WP_147053827.1|2914319_2914613_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin
MFREIVWSQRAIKEWIKILEYWNERNKSYAYSLKLDHLVKASFAIVANSPEIGKATDSPSIRIKVILDYLFYYRITPGHIEILSVWDSRRNPKKFKL
>NZ_CP042437.1|WP_147053826.1|2912481_2914227_-|aspartate--tRNA-ligase
MLRTHTCGELNISNLGQSVTLCGWVQKSRDLGGTTFIDVRDRYGLTQLVFNTDTDALLREKSRELGREFVIQVTGKVLERSNKNTKIPTGEIEIAVAGIEILNSAKIPPFLIEDETDGGEELRAKYRYLDLRRAPVRNNLILRHKMAQEIRRYLSDIDFLEVETPVLIKSTPEGARDFVVPSRMNPGEFYALPQSPQTFKQLLMVSGFDRYFQIVKCFRDEDLRADRQPEFTQIDCELSFITQEDILNIFEGLTRHLFTTVKGIDLGDFPRMQYADAMRLYGSDKPDVRFGMEFVELNDIVKGKGFGVFDNAELVVGINAKGCASYTRKQLDEITEWLKRPQIGVAGMIYCRYNEDGTLKSSVDKFYSEDELNNWAAAFEAERGDLMLVLAGNADKVRKQLNELRLEMGSRLGLRDKNKFAPLWVLDFPLLEWDEETGRYHAMHHPFTSPKPEDIALLDTDPGAVRANAYDLVINGTEVGGGSIRIHDRAMQSLMFKHLGFSSEEAQKQFGFLMDAFEYGAPPHGGLALGFDRLVSIFAGLDSIRDVIAFPKNNSGRDVMIDSPSTIADTQLKELNIKTTV
>NZ_CP042437.1|WP_147053825.1|2911939_2912419_-|hypothetical-protein
MKKILLLLLLPMAMLSSSCLKSNNNVVPFDAAKQAATDETTIQAYLAAHTEIHAVKDTTGVYYQIITQGTGATPALTSTISAAYTGKLTNGTIFDSSTNLVYKLNGLIPAWQIALPYLKTGGQMLIITPSRYAYGNAQAGIIPANSVLIFSVNLTAVAN
>NZ_CP042437.1|WP_158642888.1|2911278_2911758_-|peptidylprolyl-isomerase
MKKLLLLILFPLALYSLSSCTKVSDPTITTAIQQAADDDAAIKAYLTVHPEITNVKDTLGCYYQVVSTGAGAYPTATTTIKGTYTGSLLGGTAFATNASISAPLSSLIYGWQIVLPHVPIGSKIIMLIPSIYGYGTSGSGAIPANAVLRFDVDLSPPGA
>NZ_CP042437.1|WP_147053823.1|2910952_2911180_-|hypothetical-protein
MNKLLLLFAAVIGISSCKTAPQVDAVKQARIDDSLIRVYLSNNPVVKAVKIRRDCTTRLLNRVRAPQQPSILRLR
>NZ_CP042437.1|WP_147053822.1|2910722_2911019_-|hypothetical-protein
MYYQVVKPGTGAAATINSTVTVNYRGKLLNGPPFDSANGYSSPLAALVRGWQIGVPHIKAGGNIVLFVPSALGYGGASLGPIPPNSVLIFDIDLTGVK
>NZ_CP042437.1|WP_147053821.1|2909307_2910603_-|amidohydrolase
MKLRIAPLFLVFATQVFAQQSQVSTKADALKDQVIAWRRDFHEHPELGNHEVRTSAIIAKHLQSLGIQVQTGVATTGVVGILKGGKPGPVVALRADMDGLPVVERTDVPFASKVKTTYNGQEVGVMHACGHDSHMAILMGVAQVLSGMKNELHGTVKFIFQPAEEGVEPGQKGGAEEMVKEGVLENPKVDVVFGLHINSQTEVGKITYRPGGTMAGVNDMQIIVKGRSAHGAYPWSSVDPIVVSAEIINNLQTIVSRNINITENPAVVTIGSIKGGNRSNIIPESVEMLGTLRSFTAADEKMLVERVKQIATKTAEAQGATAEVKIPYSSHYPVTYNDPALTQQMLPSLQKTAGADNVMLKPPVTGAEDFSFYQEKVPGMFIFLGGMPKGADPLKAPSHHTPDFYIDESGFSLGVKALCNLTLDYMNAKGK
>NZ_CP042437.1|WP_147053820.1|2908699_2909206_-|DUF4440-domain-containing-protein
MRKSILTMVYTSLLLILITSQKTIAADMAAEDTVKKINPEVLQTINTVLKASYTFDIDKVTDVYAPNAVVTDEQQPYSWNGQLAGVQWVNSVQKAVSDFKIRDFTVNIKKIKIFQQTEEVAYLIVPVEYTGTVNGDPFNEEGAFSFVFRYVSGKWLIKSQAWVPKNGL
>NZ_CP042437.1|WP_147053829.1|2917978_2918617_+|nicotinamide-mononucleotide-transporter
MHDLIKLFIDQIKETTWVQWLAVALGVAEVLLARKNNIWLYPAGILGTAIAIYLLLNVGLYAESILNGYYVIMSVYGWWYWVKRRNEPPVEISWSTKNEWGISIAISVIGWIFFYVLLKNLPAKYFTPSNVPVWDALISSTAWAGMWLLARRKIENWIFLNISNLFAVPILFYKHLPMFALLTIFLFVVAIFGYFDWAARVKSQESRVKTGN
>NZ_CP042437.1|WP_147053830.1|2918748_2919834_+|acyl-CoA-dehydrogenase
MPHPSYLLKPEWVKTIRDTGAEAEKLAMLHPDQLKLVYEQGWFKFLVPKAYSGLQLPLPDMVRLEESLAWANGSLGWVVTLCSGAGWFGGFLSADVAPELLNNPALCLAGSGASTGTATITDGGYIINGTWKYASGAHHATHITANCIIKNGDEPVLDADGNELILPFIFDKKDVEIFPAWKYIGMMATGSDAYQVSNLFVKANRCFKIDPAYAVINEPLYKYPFLQLAEATLAANISGMAVHFLDLCGPLFDEKQLGKRQPGTYRDATKQLLDELTAKLNNTRAEFYRAVDASWQSGLTGPAGYLTEVSATSRKLAKTARESVDKLYPYCGLQAANPDTEISQTWRDLHTASQHSLLNSI
>NZ_CP042437.1|WP_147053831.1|2920080_2921799_+|alkaline-phosphatase-family-protein
MKLKYLLLLILATASLSASAQSHKKKHKHTARRNSDSEITYHRERSMPMPTGLPRPKLVIGLVVDQMRWDYLYRYFDRYEDGGFKRMLGEGFTCENTNIDYIPTVTAAGHTCIYTGSVPAIHGIAGNDFIVQATGKSMYCTDDSTVTAVGSTSKAGQMSPRNLLVTTVTDELRLATNFRSKVIGIALKDRGGILPAGHTANAAYWFDDASGNWISSTYYMTDLPAWVKNFNSQKIAEKYLKQDWNTLYPIATYLQSAPDNSGKYEGKFAGTSAPTMPVNTSALYNGHLGMIRSTPYGNSMTLDMAKAAIENEQLGKNTVTDFLAVSLSSTDYIGHQFGPNSVEIEDTYLRLDHDLAAFFAYLDGTLGKGSYSVFLTADHGAAHNATFLKDHNVPAGTWDDAAAQKEMNTVLNDKYKVQNLVISMDNYQVNLNNAAIKKAGISEAAIRLDCISYLQKQPAVQFAVDMQNANDATIPVDLRSRIVNGYNTEHSGVIQIVLKPGYYSGHGATGTTHGTWAPYDTHIPLVFMGWGINHGNTTRQTHMTDIAPTVASLLHIQAPDGCIGKTISEVIR
>NZ_CP042437.1|WP_147053832.1|2922023_2922647_+|thiamine-phosphate-synthase
MKKYISRFHYITQDMPQRSHIQQVEIACNAGANWIQYRCNTKPENELIAEIDQIAAICDDWGATLIITNHYQLLDKVDAQGVHIEDEAADFSAIREAINDDKTLGASATNLAGLLKTQDSGIVDYCVLGPFAHTETRPNNFPLLGYDGYRQLEKAPVEIPVIATGGIQLQDVELLLKTGIYGIAVSSAINRSVDPGGMVKEFYRKVY
>NZ_CP042437.1|WP_147053833.1|2922881_2923670_+|hypothetical-protein
MESYNRLWRLFFAIALVSIAVQQFICSGFRPVIMPPEPAFIGQSTFCMCVSGILLILVSAAIISGINSHIVADYLGAFMLLMIILSHVPYNIKINQLFLAGWNDAFKLLALCGGAFIVATSIPSDKVSGIDAVTEKIRPAGPYFFATTMIVFGIEHFIYPKFVALLVPSWIPFHLFWVCFAGIALIAAGVAIMLKFKVKLAASLLGLMLFLWLIMVHIPRGLDTSIVDHANEWTSVFEALAFSGIAFLIAGTYKPAQTAASQ
>NZ_CP042437.1|WP_147053834.1|2923740_2924169_+|cytochrome-B
MTAYSFLQHLHSGFRYIVLALILAAIIGAFIGLTGKKPYTNGNRKLNLFAMISAHTQLLIGIVLYFVSPLVQFNSETMKNKVTRYFTVEHWVIMLIALALITIGHSKSKKAATGEAKHKAIVTFYLIALVIILAGIILIPRS
>NZ_CP042437.1|WP_147053835.1|2924403_2925813_+|anthranilate-synthase-component-I-family-protein
MSTFKITTTHKKLLADTTTPVSIYLRLRDVFPNSLLLESSDYHSRENSLSYICCEPIAGFVLNNGILKKHYPDGSGESLEAGSFELIDQLNQFVGSFETDPNPLKIISNGLFGYFTHEAVEHFETIKLKQTDDNPRQIPVMQYHIYRYIIAVDHFKNELYIFHNQAEGGPTNGGIEKLEYLIKNKNFPEYSFKSSDVEKSNLTNEEFIAIVEKMKQHIYRGDVFQIVPSRAFSRTFQGDEFNVYRALRSINPSPYLFYFDYGDFRIFGSSPEAQITIKNNVASIFPIAGTFKRSGDDEKDAEIARNLENDPKESAEHVMLVDLARNDLSRHCEQVQVKAFKEVQYYSHLIHLVSHVSGKLLPGVSSFKIVADTYPAGTLSGAPKYRAMEIIDENEKAKRSFYSGAIGFMGFNGEFNHAIMIRSFLSKNNTLHYQAGAGIVAGSVAESELKEVDNKIAALRRAVELAEEL
>NZ_CP042437.1|WP_147053836.1|2925887_2926505_+|C26-family-cysteine-hydrolase-domain-containing-family
MNEHINSPFRGPGGQGGNILIIDNYDSFTYNLVHLVNELGLQCEVWRNDKFALEDVDAYDKIILSPGPGIPSEAGLLLDVIKKYAPTKSIFGVCLGQQAIAEVFGGSLYNLSQPMHGIATPIKVTDADEQLFRDLPGNFKVGRYHSWVVSANDLPEVLKVTAIDEEDNSIMALSHREYDVRGVQFHPESILTEYGKEMMGNWLNG
>NZ_CP042437.1|WP_147053837.1|2926714_2927497_+|indole-3-glycerol-phosphate-synthase-TrpC
MTILDKIVANKKKEVAYAKKRTSYIELEESEYFHRETYSFKDFLLDPARTGIIAEFKRKSPSKGIINDKVRVSKVTTDYAAAGASALSVLTDRDFFMGRKADLKKARSVNNIPVLRKDFMIDEYQVIEAKALGADIILLIAAILTPAEIDKLATLAKSLDLNVLLEVHNLEELERSIHPKLDAIGVNNRNLADFTVSVETSYQLAKHIPAEFMKISESAISDPETIRHLKLAGFNGFLIGETFMKQQDPGLAMREFVAQL
>NZ_CP042437.1|WP_147053838.1|2927888_2929355_-|SusD/RagB-family-nutrient-binding-outer-membrane-lipoprotein
MKKILGVFLLTSIVFSACKKDLTSLNNDPKNPSIVPSYALFTNAQRRLTNTVTSSNVNLNIFRLIEQQWQETTYTDESNYDITTRPIPDDIWNALYRDVIYNFERTKALIPTDVTGADIQKNEIAITDVMQVYTYYYLVTTFGDIPYTEALDISKPFPKFDDAKTVYYSLLTRLDADIAALNTGAASFGSADVIYGGDVTKWKKFAATLKLKMGITIADLDNAKAKTVVESAVATGVFTSNSDNAQFQYLTSPPNTNPVWVDLVQSARQDFVACSTIMGFLKPQTAFADPRLPYYFTVNSAGTYTGADPGSSATFSLFSKPSGPLLVSSSIGKITNPDFPGLLLDYSETEFNLAEAISRGYAVAGSVAGHYNSAVTASITYWGASATAAAAYLLQPTVAFATATGGTDLHKIGLQKYLALYNRGWDAWTETRRLDYPVLTAPSTAQTAFPVRLTYPVNEQNVNVTNYNKAATAIGGDLVTTKLFFDKH

Crispr_ID: NZ_CP042437_7

• CRISPR_ID: NZ_CP042437_7
• CRISPR_location: 2921849-2921933
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_7

Consensus_repeat	Method
TTGACATTTTACCGGCAACACGCCC	CRISPRCasFinder

spacers of NZ_CP042437_7

>7.1|2921874|35|NZ_CP042437|CRISPRCasFinder
TTCGCAACACGAACCACATAGCCAGGTTCAGGAAT

CRISPR arrays and Neighbor proteins around NZ_CP042437_7

CRISPR arrays

The CRISPR arrays of NZ_CP042437_7

>merge|NZ_CP042437|7|2921849-2921933|CRISPRCasFinder
TTGACATTTTACCGGCAACACGCCCTTCGCAACACGAACCACATAGCCAGGTTCAGGAATTTGATATTTTACCGGCAACACGCCC

>NZ_CP042437|7|7|2921849-2921933|CRISPRCasFinder
TTGACATTTTACCGGCAACACGCCC	TTCGCAACACGAACCACATAGCCAGGTTCAGGAAT
TTGATATTTTACCGGCAACACGCCC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147053837.1|2926714_2927497_+|indole-3-glycerol-phosphate-synthase-TrpC	unknown	unknown	gnl|CDD|234710
NZ_CP042437.1|WP_147053838.1|2927888_2929355_-|SusD/RagB-family-nutrient-binding-outer-membrane-lipoprotein	unknown	unknown	gnl|CDD|378943
NZ_CP042437.1|WP_147053827.1|2914319_2914613_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	unknown	unknown	gnl|CDD|368240
NZ_CP042437.1|WP_147053841.1|2936059_2938237_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053836.1|2925887_2926505_+|C26-family-cysteine-hydrolase-domain-containing-family	unknown	unknown	gnl|CDD|223586
NZ_CP042437.1|WP_158642888.1|2911278_2911758_-|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|223619
NZ_CP042437.1|WP_147053839.1|2929366_2932606_-|SusC/RagA-family-TonB-linked-outer-membrane-protein	unknown	unknown	gnl|CDD|274948
NZ_CP042437.1|WP_147060957.1|2915268_2917701_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP042437.1|WP_147053830.1|2918748_2919834_+|acyl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173848
NZ_CP042437.1|WP_147053832.1|2922023_2922647_+|thiamine-phosphate-synthase	unknown	unknown	gnl|CDD|238317
NZ_CP042437.1|WP_147053833.1|2922881_2923670_+|hypothetical-protein	unknown	unknown	gnl|CDD|226720
NZ_CP042437.1|WP_147053829.1|2917978_2918617_+|nicotinamide-mononucleotide-transporter	unknown	unknown	gnl|CDD|377432
NZ_CP042437.1|WP_147053825.1|2911939_2912419_-|hypothetical-protein	unknown	unknown	gnl|CDD|223619
NZ_CP042437.1|WP_147053828.1|2914597_2914837_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053834.1|2923740_2924169_+|cytochrome-B	unknown	unknown	unknown
NZ_CP042437.1|WP_147053835.1|2924403_2925813_+|anthranilate-synthase-component-I-family-protein	unknown	unknown	gnl|CDD|223225
NZ_CP042437.1|WP_147053826.1|2912481_2914227_-|aspartate--tRNA-ligase	unknown	unknown	gnl|CDD|234775
NZ_CP042437.1|WP_147053831.1|2920080_2921799_+|alkaline-phosphatase-family-protein	unknown	unknown	gnl|CDD|293740
NZ_CP042437.1|WP_147053840.1|2933203_2935486_-|glycoside-hydrolase-family-92-protein	unknown	unknown	gnl|CDD|377950
NZ_CP042437.1|WP_147053823.1|2910952_2911180_-|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147053837.1|2926714_2927497_+|indole-3-glycerol-phosphate-synthase-TrpC	gnl|CDD|234710	PRK00278, trpC, indole-3-glycerol phosphate synthase TrpC.	3.80347e-109
NZ_CP042437.1|WP_147053838.1|2927888_2929355_-|SusD/RagB-family-nutrient-binding-outer-membrane-lipoprotein	gnl|CDD|378943	pfam12771, SusD-like_2, Starch-binding associating with outer membrane. SusD is a secreted starch-binding protein with an N-terminal lipid tail that allows it to associate with the outer membrane.	2.66267e-144
NZ_CP042437.1|WP_147053827.1|2914319_2914613_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin	gnl|CDD|368240	pfam05016, ParE_toxin, ParE toxin of type II toxin-antitoxin system, parDE. ParE is the toxin family of a type II toxin-antitoxin family. It is toxic towards DNA gyrase, but is neutralized by the antitoxin ParD. The family also encompasses RelE/ParE described in.	9.86712e-05
NZ_CP042437.1|WP_147053836.1|2925887_2926505_+|C26-family-cysteine-hydrolase-domain-containing-family	gnl|CDD|223586	COG0512, PabA, Anthranilate/para-aminobenzoate synthases component II [Amino acid transport and metabolism / Coenzyme metabolism].	8.47393e-92
NZ_CP042437.1|WP_147053833.1|2922881_2923670_+|hypothetical-protein	gnl|CDD|226720	COG4270, COG4270, Predicted membrane protein [Function unknown].	0.00339736
NZ_CP042437.1|WP_147053835.1|2924403_2925813_+|anthranilate-synthase-component-I-family-protein	gnl|CDD|223225	COG0147, TrpE, Anthranilate/para-aminobenzoate synthases component I [Amino acid transport and metabolism / Coenzyme metabolism].	3.66672e-140
NZ_CP042437.1|WP_147053830.1|2918748_2919834_+|acyl-CoA-dehydrogenase	gnl|CDD|173848	cd01159, NcnH, Naphthocyclinone hydroxylase. Naphthocyclinone is an aromatic polyketide and an antibiotic, which is active against Gram-positive bacteria. Polyketides are secondary metabolites, which have important biological functions such as antitumor, immunosupressive or antibiotic activities. NcnH is a hydroxylase involved in the biosynthesis of naphthocyclinone and possibly other polyketides.	2.80757e-52
NZ_CP042437.1|WP_158642888.1|2911278_2911758_-|peptidylprolyl-isomerase	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	4.81278e-22
NZ_CP042437.1|WP_147053839.1|2929366_2932606_-|SusC/RagA-family-TonB-linked-outer-membrane-protein	gnl|CDD|274948	TIGR04056, OMP_RagA_SusC, TonB-linked outer membrane protein, SusC/RagA family. This model describes a distinctive clade among the TonB-linked outer membrane proteins (OMP). Members of this family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 alone. Published descriptions of members of this family are available for RagA from Porphyromonas gingivalis, SusC from Bacteroides thetaiotaomicron, and OmpW from Bacteroides caccae. Members form pairs with members of the SusD/RagB family (pfam07980). Transporter complexes including these outer membrane proteins are likely to import large degradation products of proteins (e.g. RagA) or carbohydrates (e.g. SusC) as nutrients, rather than siderophores. [Transport and binding proteins, Unknown substrate].	7.53883e-180
NZ_CP042437.1|WP_147053829.1|2917978_2918617_+|nicotinamide-mononucleotide-transporter	gnl|CDD|377432	pfam04973, NMN_transporter, Nicotinamide mononucleotide transporter. Members of this family are integral membrane proteins that are involved in transport of nicotinamide mononucleotide.	5.17444e-46
NZ_CP042437.1|WP_147053825.1|2911939_2912419_-|hypothetical-protein	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	3.43086e-29
NZ_CP042437.1|WP_147060957.1|2915268_2917701_+|TonB-dependent-receptor	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	4.89454e-28
NZ_CP042437.1|WP_147053826.1|2912481_2914227_-|aspartate--tRNA-ligase	gnl|CDD|234775	PRK00476, aspS, aspartyl-tRNA synthetase; Validated.	0
NZ_CP042437.1|WP_147053832.1|2922023_2922647_+|thiamine-phosphate-synthase	gnl|CDD|238317	cd00564, TMP_TenI, Thiamine monophosphate synthase (TMP synthase)/TenI. TMP synthase catalyzes an important step in the thiamine biosynthesis pathway, the substitution of the pyrophosphate of 2-methyl-4-amino-5- hydroxymethylpyrimidine pyrophosphate by 4-methyl-5- (beta-hydroxyethyl) thiazole phosphate to yield thiamine phosphate. TenI is a enzymatically inactive regulatory protein involved in the regulation of several extracellular enzymes. This superfamily also contains other enzymatically inactive proteins with unknown functions.	2.76738e-45
NZ_CP042437.1|WP_147053831.1|2920080_2921799_+|alkaline-phosphatase-family-protein	gnl|CDD|293740	cd16016, AP-SPAP, SPAP is a subclass of alkaline phosphatase (AP). Alkaline phosphatases are non-specific phosphomonoesterases that catalyze the hydrolysis reaction via a phosphoseryl intermediate to produce inorganic phosphate and the corresponding alcohol, optimally at high pH. Alkaline phosphatase exists as a dimer, each monomer binding 2 zinc atoms and one magnesium atom, which are essential for enzymatic activity. Although SPAP is a subclass of alkaline phosphatase, SPAP has many differences from other APs: 1) the catalytic residue is a threonine instead of serine, 2) there is no binding pocket for the third metal ion, and 3) the arginine residue forming bidentate hydrogen bonding is deleted in SPAP. A lysine and an asparagine residue, recruited together for the first time into the active site, bind the substrate phosphoryl group in a manner not observed before in any other AP.	5.41543e-127
NZ_CP042437.1|WP_147053840.1|2933203_2935486_-|glycoside-hydrolase-family-92-protein	gnl|CDD|377950	pfam07971, Glyco_hydro_92, Glycosyl hydrolase family 92. Members of this family are alpha-1,2-mannosidases, enzymes which remove alpha-1,2-linked mannose residues from Man(9)(GlcNAc)(2) by hydrolysis. They are critical for the maturation of N-linked oligosaccharides and ER-associated degradation.	0

Protein sequences

>NZ_CP042437.1|WP_147053831.1|2920080_2921799_+|alkaline-phosphatase-family-protein
MKLKYLLLLILATASLSASAQSHKKKHKHTARRNSDSEITYHRERSMPMPTGLPRPKLVIGLVVDQMRWDYLYRYFDRYEDGGFKRMLGEGFTCENTNIDYIPTVTAAGHTCIYTGSVPAIHGIAGNDFIVQATGKSMYCTDDSTVTAVGSTSKAGQMSPRNLLVTTVTDELRLATNFRSKVIGIALKDRGGILPAGHTANAAYWFDDASGNWISSTYYMTDLPAWVKNFNSQKIAEKYLKQDWNTLYPIATYLQSAPDNSGKYEGKFAGTSAPTMPVNTSALYNGHLGMIRSTPYGNSMTLDMAKAAIENEQLGKNTVTDFLAVSLSSTDYIGHQFGPNSVEIEDTYLRLDHDLAAFFAYLDGTLGKGSYSVFLTADHGAAHNATFLKDHNVPAGTWDDAAAQKEMNTVLNDKYKVQNLVISMDNYQVNLNNAAIKKAGISEAAIRLDCISYLQKQPAVQFAVDMQNANDATIPVDLRSRIVNGYNTEHSGVIQIVLKPGYYSGHGATGTTHGTWAPYDTHIPLVFMGWGINHGNTTRQTHMTDIAPTVASLLHIQAPDGCIGKTISEVIR
>NZ_CP042437.1|WP_147053830.1|2918748_2919834_+|acyl-CoA-dehydrogenase
MPHPSYLLKPEWVKTIRDTGAEAEKLAMLHPDQLKLVYEQGWFKFLVPKAYSGLQLPLPDMVRLEESLAWANGSLGWVVTLCSGAGWFGGFLSADVAPELLNNPALCLAGSGASTGTATITDGGYIINGTWKYASGAHHATHITANCIIKNGDEPVLDADGNELILPFIFDKKDVEIFPAWKYIGMMATGSDAYQVSNLFVKANRCFKIDPAYAVINEPLYKYPFLQLAEATLAANISGMAVHFLDLCGPLFDEKQLGKRQPGTYRDATKQLLDELTAKLNNTRAEFYRAVDASWQSGLTGPAGYLTEVSATSRKLAKTARESVDKLYPYCGLQAANPDTEISQTWRDLHTASQHSLLNSI
>NZ_CP042437.1|WP_147053829.1|2917978_2918617_+|nicotinamide-mononucleotide-transporter
MHDLIKLFIDQIKETTWVQWLAVALGVAEVLLARKNNIWLYPAGILGTAIAIYLLLNVGLYAESILNGYYVIMSVYGWWYWVKRRNEPPVEISWSTKNEWGISIAISVIGWIFFYVLLKNLPAKYFTPSNVPVWDALISSTAWAGMWLLARRKIENWIFLNISNLFAVPILFYKHLPMFALLTIFLFVVAIFGYFDWAARVKSQESRVKTGN
>NZ_CP042437.1|WP_147060957.1|2915268_2917701_+|TonB-dependent-receptor
MALLLPVLASAQLSISGKVTNQSGEALPGATITINNPAASVVADATGKYGFTNLKPGSYTLNASFIGYQTISKNIVLAANQVINLALVNGTLAAEEVTISATRAVKNSPTAFTNLSKKDLAKNNFGQDLPYLLSLTPSVVTTSDAGAGIGYTGIRIRGSDNTRVNVTINGIPLNDAESQGSYFIDLPDLASSVDNIQVQRGVGTSTNGAGAFGGSINIQTTTRRDTAYAEINTSAGSYGSIKNTVNAGTGLLDGHFSLDGRLSRIHSNGYIDRATSDLKSLYLSAAWYGKNSTIRANVISGHERTYQAWNGIADYVIGDNTRKDNRTYNELGLMDDAGNFYKDQVDDYLQNHYQLLYDQKISSKLSFSGALHYTKGKGYYEEYRRQDAVANYGLTPVIMGMDTIKTTDLVRRLWLDNEFYGVTYALKYQPQSNLNMTLGGAYNEYKGAHYGNIIYTKESAGIGPNYEYYRDNAKKNDFNIFYRAEWHLNKVLLYADAQYRHLYYNFYGIDKNQQNAQQSIELNFFNPKVGITYQLNEQNNVYASFAVGNHEPNRDDYVNSTPQARPKAENLKDFEAGYRTVGKIFSGGINGFYMLYKNQLILTGALNDVGGAIRTNVPDSYRTGVELDGKVRITSQLNWGITATWSANKIKNYHQFFSNYDDGTLVEESFKKTTIAYSPSLTGASIISYSPVKGGEIAFISKYVGKQYLDNTMNQNPAGFNIAPDNQSNPYAANRYLKSYFTSDVRLRYNFSISQVKNIGLGLQVNNVFSKKYEANGATYPDIEGGNMVNYNYYFPQAPRNFMAMLSLNF
>NZ_CP042437.1|WP_147053828.1|2914597_2914837_-|hypothetical-protein
MLTDIEIKEKLIATISNTDNMELLRELLMITEMEDEISGVYQLSPEEIIAVNEGIEQIEKGMFVTNEEANKLIDKCLGR
>NZ_CP042437.1|WP_147053827.1|2914319_2914613_-|type-II-toxin-antitoxin-system-RelE/ParE-family-toxin
MFREIVWSQRAIKEWIKILEYWNERNKSYAYSLKLDHLVKASFAIVANSPEIGKATDSPSIRIKVILDYLFYYRITPGHIEILSVWDSRRNPKKFKL
>NZ_CP042437.1|WP_147053826.1|2912481_2914227_-|aspartate--tRNA-ligase
MLRTHTCGELNISNLGQSVTLCGWVQKSRDLGGTTFIDVRDRYGLTQLVFNTDTDALLREKSRELGREFVIQVTGKVLERSNKNTKIPTGEIEIAVAGIEILNSAKIPPFLIEDETDGGEELRAKYRYLDLRRAPVRNNLILRHKMAQEIRRYLSDIDFLEVETPVLIKSTPEGARDFVVPSRMNPGEFYALPQSPQTFKQLLMVSGFDRYFQIVKCFRDEDLRADRQPEFTQIDCELSFITQEDILNIFEGLTRHLFTTVKGIDLGDFPRMQYADAMRLYGSDKPDVRFGMEFVELNDIVKGKGFGVFDNAELVVGINAKGCASYTRKQLDEITEWLKRPQIGVAGMIYCRYNEDGTLKSSVDKFYSEDELNNWAAAFEAERGDLMLVLAGNADKVRKQLNELRLEMGSRLGLRDKNKFAPLWVLDFPLLEWDEETGRYHAMHHPFTSPKPEDIALLDTDPGAVRANAYDLVINGTEVGGGSIRIHDRAMQSLMFKHLGFSSEEAQKQFGFLMDAFEYGAPPHGGLALGFDRLVSIFAGLDSIRDVIAFPKNNSGRDVMIDSPSTIADTQLKELNIKTTV
>NZ_CP042437.1|WP_147053825.1|2911939_2912419_-|hypothetical-protein
MKKILLLLLLPMAMLSSSCLKSNNNVVPFDAAKQAATDETTIQAYLAAHTEIHAVKDTTGVYYQIITQGTGATPALTSTISAAYTGKLTNGTIFDSSTNLVYKLNGLIPAWQIALPYLKTGGQMLIITPSRYAYGNAQAGIIPANSVLIFSVNLTAVAN
>NZ_CP042437.1|WP_158642888.1|2911278_2911758_-|peptidylprolyl-isomerase
MKKLLLLILFPLALYSLSSCTKVSDPTITTAIQQAADDDAAIKAYLTVHPEITNVKDTLGCYYQVVSTGAGAYPTATTTIKGTYTGSLLGGTAFATNASISAPLSSLIYGWQIVLPHVPIGSKIIMLIPSIYGYGTSGSGAIPANAVLRFDVDLSPPGA
>NZ_CP042437.1|WP_147053823.1|2910952_2911180_-|hypothetical-protein
MNKLLLLFAAVIGISSCKTAPQVDAVKQARIDDSLIRVYLSNNPVVKAVKIRRDCTTRLLNRVRAPQQPSILRLR
>NZ_CP042437.1|WP_147053832.1|2922023_2922647_+|thiamine-phosphate-synthase
MKKYISRFHYITQDMPQRSHIQQVEIACNAGANWIQYRCNTKPENELIAEIDQIAAICDDWGATLIITNHYQLLDKVDAQGVHIEDEAADFSAIREAINDDKTLGASATNLAGLLKTQDSGIVDYCVLGPFAHTETRPNNFPLLGYDGYRQLEKAPVEIPVIATGGIQLQDVELLLKTGIYGIAVSSAINRSVDPGGMVKEFYRKVY
>NZ_CP042437.1|WP_147053833.1|2922881_2923670_+|hypothetical-protein
MESYNRLWRLFFAIALVSIAVQQFICSGFRPVIMPPEPAFIGQSTFCMCVSGILLILVSAAIISGINSHIVADYLGAFMLLMIILSHVPYNIKINQLFLAGWNDAFKLLALCGGAFIVATSIPSDKVSGIDAVTEKIRPAGPYFFATTMIVFGIEHFIYPKFVALLVPSWIPFHLFWVCFAGIALIAAGVAIMLKFKVKLAASLLGLMLFLWLIMVHIPRGLDTSIVDHANEWTSVFEALAFSGIAFLIAGTYKPAQTAASQ
>NZ_CP042437.1|WP_147053834.1|2923740_2924169_+|cytochrome-B
MTAYSFLQHLHSGFRYIVLALILAAIIGAFIGLTGKKPYTNGNRKLNLFAMISAHTQLLIGIVLYFVSPLVQFNSETMKNKVTRYFTVEHWVIMLIALALITIGHSKSKKAATGEAKHKAIVTFYLIALVIILAGIILIPRS
>NZ_CP042437.1|WP_147053835.1|2924403_2925813_+|anthranilate-synthase-component-I-family-protein
MSTFKITTTHKKLLADTTTPVSIYLRLRDVFPNSLLLESSDYHSRENSLSYICCEPIAGFVLNNGILKKHYPDGSGESLEAGSFELIDQLNQFVGSFETDPNPLKIISNGLFGYFTHEAVEHFETIKLKQTDDNPRQIPVMQYHIYRYIIAVDHFKNELYIFHNQAEGGPTNGGIEKLEYLIKNKNFPEYSFKSSDVEKSNLTNEEFIAIVEKMKQHIYRGDVFQIVPSRAFSRTFQGDEFNVYRALRSINPSPYLFYFDYGDFRIFGSSPEAQITIKNNVASIFPIAGTFKRSGDDEKDAEIARNLENDPKESAEHVMLVDLARNDLSRHCEQVQVKAFKEVQYYSHLIHLVSHVSGKLLPGVSSFKIVADTYPAGTLSGAPKYRAMEIIDENEKAKRSFYSGAIGFMGFNGEFNHAIMIRSFLSKNNTLHYQAGAGIVAGSVAESELKEVDNKIAALRRAVELAEEL
>NZ_CP042437.1|WP_147053836.1|2925887_2926505_+|C26-family-cysteine-hydrolase-domain-containing-family
MNEHINSPFRGPGGQGGNILIIDNYDSFTYNLVHLVNELGLQCEVWRNDKFALEDVDAYDKIILSPGPGIPSEAGLLLDVIKKYAPTKSIFGVCLGQQAIAEVFGGSLYNLSQPMHGIATPIKVTDADEQLFRDLPGNFKVGRYHSWVVSANDLPEVLKVTAIDEEDNSIMALSHREYDVRGVQFHPESILTEYGKEMMGNWLNG
>NZ_CP042437.1|WP_147053837.1|2926714_2927497_+|indole-3-glycerol-phosphate-synthase-TrpC
MTILDKIVANKKKEVAYAKKRTSYIELEESEYFHRETYSFKDFLLDPARTGIIAEFKRKSPSKGIINDKVRVSKVTTDYAAAGASALSVLTDRDFFMGRKADLKKARSVNNIPVLRKDFMIDEYQVIEAKALGADIILLIAAILTPAEIDKLATLAKSLDLNVLLEVHNLEELERSIHPKLDAIGVNNRNLADFTVSVETSYQLAKHIPAEFMKISESAISDPETIRHLKLAGFNGFLIGETFMKQQDPGLAMREFVAQL
>NZ_CP042437.1|WP_147053838.1|2927888_2929355_-|SusD/RagB-family-nutrient-binding-outer-membrane-lipoprotein
MKKILGVFLLTSIVFSACKKDLTSLNNDPKNPSIVPSYALFTNAQRRLTNTVTSSNVNLNIFRLIEQQWQETTYTDESNYDITTRPIPDDIWNALYRDVIYNFERTKALIPTDVTGADIQKNEIAITDVMQVYTYYYLVTTFGDIPYTEALDISKPFPKFDDAKTVYYSLLTRLDADIAALNTGAASFGSADVIYGGDVTKWKKFAATLKLKMGITIADLDNAKAKTVVESAVATGVFTSNSDNAQFQYLTSPPNTNPVWVDLVQSARQDFVACSTIMGFLKPQTAFADPRLPYYFTVNSAGTYTGADPGSSATFSLFSKPSGPLLVSSSIGKITNPDFPGLLLDYSETEFNLAEAISRGYAVAGSVAGHYNSAVTASITYWGASATAAAAYLLQPTVAFATATGGTDLHKIGLQKYLALYNRGWDAWTETRRLDYPVLTAPSTAQTAFPVRLTYPVNEQNVNVTNYNKAATAIGGDLVTTKLFFDKH
>NZ_CP042437.1|WP_147053839.1|2929366_2932606_-|SusC/RagA-family-TonB-linked-outer-membrane-protein
MKKSLLTTLCIFLLAATQLYAQNHTVTGRVTAKEDGLPVPGVSVSIKGTTTGTQTDVSGKYSLSVPDNATLSFSFIGYITQSLPVNGNRMDVVLIASSQQLGEVVVTGALGISRTRNQQSYAAQQVSGDEVNKTRSSSFINGLSGKVAGLEIRQNNALGSSTNVVLRGVKSITGNNQALFVIDGVPVNNSNNNSSTQQSGGGGYDYGSPSSDINPDDIESVTVLKGAAASALYGSRGSNGVILITSKKAKKGVGITINSSVSVGEVDKSTFAKYQHSYGAGYGNYYNDPTGYFFYGDVNGDGKNDLVTPTTEDASYGAKFDPNLKVYQWDAFDKTSPNFGKATPWVAATNDPTSFFVKPVSNNQSIMITNGTDGGSFKLGFTRNDENGIIPNSSIKKNIVDLGGTYNITSKLSVGGSVNYYNINGVGRPGTGYDGASARNVMTNFRQWWEVNNDVKALKAAYDRTGKNITWNYADPLAGNLTPIFWDNPYYVRYQNFESDTRNRYIGNVNATYKPVSWLTITGRTSLDSYTELDEERKNVSSVGVPYYSRNNKSFSETNYDLLANVDKNLSKSFNLKALLGTNVRKENTQSVYSVTNGGLIVPSVYSLSNSLNTPNAPIEYKGLREVDGIFAGATLTYNNLLTLDGTIRRDKSSTLPKANNTYYYPSVAGGFIFSELLKQYTWLSYGKIRANYAQVGADAPVYSVNDTYTITPPFGASPQSAVNTTKNNPNLKPERTKSAEVGLELSFFNNRLGFDGSYYATSTFDEILPVNVSTATGYSFSYLNAGTVKNKGIELSLNGTPIRTQDFNWKMTLNFTRNRSKVTELFKDGTGEESKNLELNSYQGGVSINASLNQPFGMIRGTDYKYASNGQKIVGANGQYLQSGPNENIGNSNPDWIGGINNSFTYKGFNLSFLVDIRKGGSVFSTDMYYGLATGLYPETVYTNDLGNPVRNTLANGGGFIRPGVTESGAPNTVRVSASNYGAFGYARLPDKAFVYDASYVKLREALIGYSLPQKTISTLGPIKEVTFQLIGRNLWIIHKNLPYSDPEEGLTSGNLQGYQVGAYPTTRTISLNLKLRF
>NZ_CP042437.1|WP_147053840.1|2933203_2935486_-|glycoside-hydrolase-family-92-protein
MKKLLLLALACLPAATIAQQSARVTDPVELINPLMGTASKPSLSNGNTYPAIALPWGMNFWTPQTGRMGDGWQYTYDADKILGFKQTHQPSPWMNDYGMFSIFPETGKLKLNEKERASWFSHKAEIVKPYYYSVYLADYDVTTEITPTERAASFRFTFPKSDSSHIVIDAFDKGSYIKIIPGEQKIVGYSTKNSGAVPANFKNYFVIYVDKPFALASAWHDWKKDDGQLEYTGDHAGAVITLKTTNGEQVHLKVASSFVSIEQAELNLKRELADDKFEVTCQKAKDTWNKTLSRLNVEGGTVEQTKTFYSSLYRMLFFPNKMYEIDAKGEKIHYSPFNGKVMSGYLFAGTGFWDTFRALYPFLNLVYPSINKEMQEGLINDYKEGGWLPEWSSPGYADCMIGNNSASVVAEAYLKGMRGYDIETLYQALKHGANNEGPNATGRRGVQYYNTLGYVPYNVKINENAARTLEYAYDDFAIYQLGKALGKPKSEIEIYKKRSQNYRNIFDPQTKLMRGKNQDGTFETPFNPFKWGDAFTEGNSWHYSWGVFHDIQGLINLMGGKQQFAAKLDSVFSMPPTFDDSYYGGVIHEIREMQIANMGQYAHGNQPIQHMIYLYNHAGQPWKTQYWARETMNKLYKATPDGYCGDEDNGQTSAWYIFSAMGFYPVTPASDQYVLGAPLFKKVTINLENGKTVTITAPNNSAANKYVNSLTIDGKPYTNNWVSHKGLLSGAELNFDMIATPNKERGTKDADVPFSMSNEK
>NZ_CP042437.1|WP_147053841.1|2936059_2938237_-|hypothetical-protein
MKNIFVSCCLTMLASAVFAQQAPAPLKEKTAFQTASPWMPEIDVRSDIAIVYGTNDHPGMTFEQRVQTWRDHGYQTNFMTGIAWGDYKDYFLGKWDGKNHLGVGQVTQKGDTIFHGRDMPYVVPDASFIEYMKTAVIKRVIDVGITNIFLEEPEFWARAGYSAGFKAQWQSYYGFPWKPQDASAENTYLSSKLKYHLYYDAIEKVSSYAKAYGKSKGLNIKVFIATHSLVNYSSWQIVSPEASLASLPGIDGYIAQVWTGTSREPTYFNGLQKERVFENAYLEYGSMVSMTAPTGRKMFFLTDPIEDRQKDWSDYKRNYQATFTAKLLYPTVSDYEVMPWPERIYTHPYKVANSNEKILIPQYYSTQMQVMVNALNSMPPSANKVTGVNGIGVLMSNTLMFQRFPTHNGFEDPQFSNFYGQTLPLLKHGVPVQTVHMENLGYAASLKNIKVLVMSYANMKPVSAQIHQQLAAWVKQGGVLIYCGRDDDPYQSVMEWWDTKGNNFKAPSQHLFKLLGVNPTADSQKFNVGKGAVYVLRQNPKEYVLQAANDGNYIGTVKQAYEKDAHAGALTFKNSLYLARGPYDIVAVMDENADSKPYTVKGPVIDLFDPQLPILAEKVINPGEQALLYNVARVANKNIPQVLASASRIYNEKVAAGSYSFIAKSPVKTLNSARVLLPGQPKQIVITDSKGQNITDVKTSWDTPSKTLYLGFANSPDGIKVELKW

Crispr_ID: NZ_CP042437_8

• CRISPR_ID: NZ_CP042437_8
• CRISPR_location: 3121095-3121318
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 3 spacers

Consensus repeat of NZ_CP042437_8

Consensus_repeat	Method
TTAGCCTATCAAAACTCCGAAAAAGAGAAACGTGC	CRISPRCasFinder

spacers of NZ_CP042437_8

>8.1|3121130|28|NZ_CP042437|CRISPRCasFinder
CGGTGAATTACTCGTGGCAAACAACGAA
>8.2|3121193|28|NZ_CP042437|CRISPRCasFinder
GGCCGAACTTGCCATCGCAAATAACGAG
>8.3|3121256|28|NZ_CP042437|CRISPRCasFinder
AAACGAGTTGATTATCGCCAATAAGGAG

CRISPR arrays and Neighbor proteins around NZ_CP042437_8

CRISPR arrays

The CRISPR arrays of NZ_CP042437_8

>merge|NZ_CP042437|8|3121095-3121318|CRISPRCasFinder
CTGGCATACCAAAATACCGAGAAAGAGAAACGCGCCGGTGAATTACTCGTGGCAAACAACGAATTAGCCTATCAAAACTCCGAAAAAGAGAAACGTGCGGCCGAACTTGCCATCGCAAATAACGAGTTAGCCTATCAAAACGCCGAAAAAGAGAAACGTGCAAACGAGTTGATTATCGCCAATAAGGAGCTGGCCTACCAAAATTCCGAGAAAGAACAAAGGGC

>NZ_CP042437|8|8|3121095-3121318|CRISPRCasFinder
CTGGCATACCAAAATACCGAGAAAGAGAAACGCGC	CGGTGAATTACTCGTGGCAAACAACGAA
TTAGCCTATCAAAACTCCGAAAAAGAGAAACGTGC	GGCCGAACTTGCCATCGCAAATAACGAG
TTAGCCTATCAAAACGCCGAAAAAGAGAAACGTGC	AAACGAGTTGATTATCGCCAATAAGGAG
CTGGCCTACCAAAATTCCGAGAAAGAACAAAGGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147053986.1|3124006_3124636_-|NAD(P)H-dependent-oxidoreductase	unknown	unknown	gnl|CDD|380324
NZ_CP042437.1|WP_090652238.1|3121914_3122145_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053990.1|3129449_3130022_-|peptide-deformylase	unknown	unknown	gnl|CDD|234668
NZ_CP042437.1|WP_147053977.1|3115726_3116857_+|DUF1624-domain-containing-protein	unknown	unknown	gnl|CDD|226034
NZ_CP042437.1|WP_158642896.1|3122276_3122642_-|response-regulator	unknown	unknown	gnl|CDD|381093
NZ_CP042437.1|WP_147053975.1|3111469_3111892_-|ATP-binding-protein	unknown	unknown	gnl|CDD|379279
NZ_CP042437.1|WP_147053974.1|3111038_3111470_-|rRNA-maturation-RNase-YbeY	unknown	unknown	gnl|CDD|376735
NZ_CP042437.1|WP_147053982.1|3119779_3120517_+|heavy-metal-associated-domain-containing-protein	unknown	unknown	gnl|CDD|238219
NZ_CP042437.1|WP_147053991.1|3130042_3131272_-|insulinase-family-protein	unknown	unknown	gnl|CDD|223685
NZ_CP042437.1|WP_147053985.1|3122846_3123857_+|substrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|224525
NZ_CP042437.1|WP_147053989.1|3128702_3129329_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053976.1|3111893_3115223_-|hypothetical-protein	unknown	unknown	gnl|CDD|223496
NZ_CP042437.1|WP_147060968.1|3127074_3128160_+|P-loop-NTPase	unknown	unknown	gnl|CDD|378455
NZ_CP042437.1|WP_147053978.1|3116906_3117890_+|hypothetical-protein	unknown	unknown	gnl|CDD|293786
NZ_CP042437.1|WP_147053980.1|3118445_3118859_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147053988.1|3128308_3128587_+|NifU-family-protein	unknown	unknown	gnl|CDD|376458
NZ_CP042437.1|WP_147053981.1|3119132_3119693_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|378964
NZ_CP042437.1|WP_147053987.1|3124704_3126954_-|penicillin-binding-protein	unknown	unknown	gnl|CDD|376415
NZ_CP042437.1|WP_147053983.1|3120547_3120859_+|hypothetical-protein	unknown	unknown	gnl|CDD|293894
NZ_CP042437.1|WP_147053979.1|3118007_3118223_-|hypothetical-protein	unknown	unknown	gnl|CDD|119399

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147053986.1|3124006_3124636_-|NAD(P)H-dependent-oxidoreductase	gnl|CDD|380324	cd02149, NfsB-like, nitroreductase similar to Escherichia coli NfsB. NAD(P)H:FMN oxidoreductase family. This domain catalyzes the reduction of flavin, nitrocompound, quinones and azo compounds using NADH or NADPH as an electron donor. The enzyme is a homodimer, and each monomer binds a FMN as co-factor. This family includes FRase I in Vibrio fischeri, wihich reduces FMN into FMNH2 as part of the bioluminescent reaction. The family also includes oxygen-insensitive nitroreductases that use NADH or NADPH as an electron donor in the ping pong bi bi mechanism. This type of nitroreductase can be used in cancer chemotherapy to activate a range of prodrugs.	3.4505e-50
NZ_CP042437.1|WP_147053985.1|3122846_3123857_+|substrate-binding-domain-containing-protein	gnl|CDD|224525	COG1609, PurR, Transcriptional regulators [Transcription].	8.32419e-92
NZ_CP042437.1|WP_147053990.1|3129449_3130022_-|peptide-deformylase	gnl|CDD|234668	PRK00150, def, peptide deformylase; Reviewed.	7.80565e-72
NZ_CP042437.1|WP_147053977.1|3115726_3116857_+|DUF1624-domain-containing-protein	gnl|CDD|226034	COG3503, COG3503, Predicted membrane protein [Function unknown].	6.08287e-30
NZ_CP042437.1|WP_158642896.1|3122276_3122642_-|response-regulator	gnl|CDD|381093	cd17538, REC_D1_PleD-like, first (D1) phosphoacceptor receiver (REC) domain of response regulator PleD and similar domains. PleD contains a REC domain (D1) with the phosphorylatable aspartate, a REC-like adaptor domain (D2), and the enzymatic diguanylate cyclase (DGC) domain, also called the GGDEF domain according to a conserved sequence motif, as its output domain. The GGDEF-containing PleD response regulators are global regulators of cell metabolism in some important human pathogens. This model describes D1 of PleD and similar domains. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.26257e-20
NZ_CP042437.1|WP_147053975.1|3111469_3111892_-|ATP-binding-protein	gnl|CDD|379279	pfam13581, HATPase_c_2, Histidine kinase-like ATPase domain.	9.00923e-20
NZ_CP042437.1|WP_147053974.1|3111038_3111470_-|rRNA-maturation-RNase-YbeY	gnl|CDD|376735	pfam02130, UPF0054, Uncharacterized protein family UPF0054.	1.43954e-29
NZ_CP042437.1|WP_147053982.1|3119779_3120517_+|heavy-metal-associated-domain-containing-protein	gnl|CDD|238219	cd00371, HMA, Heavy-metal-associated domain (HMA) is a conserved domain of approximately 30 amino acid residues found in a number of proteins that transport or detoxify heavy metals, for example, the CPx-type heavy metal ATPases and copper chaperones. HMA domain contains two cysteine residues that are important in binding and transfer of metal ions, such as copper, cadmium, cobalt and zinc. In the case of copper, stoichiometry of binding is one Cu+ ion per binding domain. Repeats of the HMA domain in copper chaperone has been associated with Menkes/Wilson disease due to binding of multiple copper ions.	6.54755e-11
NZ_CP042437.1|WP_147053991.1|3130042_3131272_-|insulinase-family-protein	gnl|CDD|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	2.5565e-98
NZ_CP042437.1|WP_147053976.1|3111893_3115223_-|hypothetical-protein	gnl|CDD|223496	COG0419, SbcC, ATPase involved in DNA repair [DNA replication, recombination, and repair].	6.43268e-12
NZ_CP042437.1|WP_147060968.1|3127074_3128160_+|P-loop-NTPase	gnl|CDD|378455	pfam10609, ParA, NUBPL iron-transfer P-loop NTPase. This family contains ATPases involved in plasmid partitioning. It also contains the cytosolic Fe-S cluster assembling factor NBP35 which is required for biogenesis and export of both ribosomal subunits.	1.45942e-135
NZ_CP042437.1|WP_147053978.1|3116906_3117890_+|hypothetical-protein	gnl|CDD|293786	sd00045, ANK, ankyrin repeats. Ankyrin repeats are one of the most abundant repeat motifs, and generally function as scaffolds for protein-protein interactions in processes including cell cycle, transcriptional regulation, signal transduction, vesicular trafficking, and inflammatory response. Although predominantly found in eukaryotic proteins, they are also found in some bacterial and viral proteins. Less is known of their physiological roles in prokaryotes. Some bacterial ANK proteins play key roles in microbial pathogenesis by mimicking or manipulating host function(s). The pathogen Providencia alcalifaciens N-formyltransferase ankyrin repeats function in small molecule binding and allosteric control. Ankyrin-repeat proteins have been associated with a number of human diseases.	1.35622e-18
NZ_CP042437.1|WP_147053988.1|3128308_3128587_+|NifU-family-protein	gnl|CDD|376458	pfam01106, NifU, NifU-like domain. This is an alignment of the carboxy-terminal domain. This is the only common region between the NifU protein from nitrogen-fixing bacteria and rhodobacterial species. The biochemical function of NifU is unknown.	1.04347e-28
NZ_CP042437.1|WP_147053981.1|3119132_3119693_+|helix-turn-helix-domain-containing-protein	gnl|CDD|378964	pfam12833, HTH_18, Helix-turn-helix domain.	1.37193e-19
NZ_CP042437.1|WP_147053987.1|3124704_3126954_-|penicillin-binding-protein	gnl|CDD|376415	pfam00912, Transgly, Transglycosylase. The penicillin-binding proteins are bifunctional proteins consisting of transglycosylase and transpeptidase in the N- and C-terminus respectively. The transglycosylase domain catalyzes the polymerization of murein glycan chains.	1.03364e-53
NZ_CP042437.1|WP_147053983.1|3120547_3120859_+|hypothetical-protein	gnl|CDD|293894	cd03693, EF1_alpha_II, Domain II of elongation factor 1-alpha. This family represents domain II of elongation factor 1-alpha (EF-1A) that is found in archaea and all eukaryotic lineages. EF-1A is very abundant in the cytosol, where it is involved in the GTP-dependent binding of aminoacyl-tRNAs to the A site of the ribosomes in the second step of translation from mRNAs to proteins. Both domain II of EF-1A and domain IV of IF2/eIF5B have been implicated in recognition of the 3'-ends of tRNA. More than 61% of eukaryotic elongation factor 1A (eEF-1A) in cells is estimated to be associated with actin cytoskeleton. The binding of eEF-1A to actin is a noncanonical function that may link two distinct cellular processes, cytoskeleton organization and gene expression.	0.006035
NZ_CP042437.1|WP_147053979.1|3118007_3118223_-|hypothetical-protein	gnl|CDD|119399	cd00082, HisKA, Histidine Kinase A (dimerization/phosphoacceptor) domain; Histidine Kinase A dimers are formed through parallel association of 2 domains creating 4-helix bundles; usually these domains contain a conserved His residue and are activated via trans-autophosphorylation by the catalytic domain of the histidine kinase. They subsequently transfer the phosphoryl group to the Asp acceptor residue of a response regulator protein. Two-component signalling systems, consisting of a histidine protein kinase that senses a signal input and a response regulator that mediates the output, are ancient and evolutionarily conserved signaling mechanisms in prokaryotes and eukaryotes.	0.000489336

Protein sequences

>NZ_CP042437.1|WP_147053983.1|3120547_3120859_+|hypothetical-protein
MHGDNRVNNIKCGSFLLQDYFRITGRGLVVAGELVDGTISPGNLICICHLIIKVKSVEFVRRSGGELIGLMLDIADDKGIEILVDKLKDELAHEKHPAYLILA
>NZ_CP042437.1|WP_147053982.1|3119779_3120517_+|heavy-metal-associated-domain-containing-protein
MTHTYNITGMTCTGCRAKVQSLLSQVNHIQKVDISLAEGTADITMNRHVATADLQEALAAYPKYQITDTAPHHPDTLAIVDNTGNKTWLQTYKPILLIFGYITVVAFIAGYHAKSFDIMTAMRIFMSGFFLVFSFFKLLDVEGFADSYAMYDVVARKWHGWGRLYVFIELGLGLAFAFNFTPYIVNIVTIVIMSISLIGVLKSVVSKQQIRCACLGAVFNLPMSTVTIIEDGLMIAMGVTMLLIL
>NZ_CP042437.1|WP_147053981.1|3119132_3119693_+|helix-turn-helix-domain-containing-protein
MKLYIKNMVCSRCKMVVRSELEKAGLQVLGVELGEVEIKNPPTNLQQMKLTASLKQLGFELIDDQKSRLIEQIKTTIIGQVHYADAPAPLKLSAILADKLNYDYGYLSNLFSEVEGSTIEKYYINQRTEKVKELLVYNELSLSQIAFQLGYSSVAYLSSQFKQVTGMTPSAFKKLQGNKRKNIEDL
>NZ_CP042437.1|WP_147053980.1|3118445_3118859_+|hypothetical-protein
MSFLNDPLFKALFFTDTPRIILKADAPNFTILTYNEAYMKATYTHYRNIVGWYLWEAFDPKHAGSDGDKFLLDTLTRAVVNNETIVTPPFHYNIPSANPDIIVESWWQLDIIPIAGKNKKPAFLLLTTNNITDKIIT
>NZ_CP042437.1|WP_147053979.1|3118007_3118223_-|hypothetical-protein
MISRIQSHVVRAPLARIMGLLPLVKELSGHNDEREKMFEYLMSSANELDELIKNITDKTTRADYPVIQKGK
>NZ_CP042437.1|WP_147053978.1|3116906_3117890_+|hypothetical-protein
MIQPYEMSLGLPMEVANKVISTTDKVWQILTASREGNLEAVKRLVDECPELIYAQYNYTPPIHFAAREGHTELVRYLLKQGAHDSNYKTYPFLERLELMADRGHDEIVDLLNDYATHPERQKYFGDNGKIFFNRTPLQLEFEKAVYDGDIEHTARILKDNPEFAPDETYFWGEGILTFAAKVNNRPMADVLLSYGAKVPDILKWTQKYYFERIDGATYMMENGMSPNTMSWHHVTILHDMAQKGDLAKAELLLKHGANINALDEEYQSTPLGMAARWGHFDMAGYLLKQGADPNKSGAPWSAPLAWAIRKGHSEIEGLLRQYGAIDI
>NZ_CP042437.1|WP_147053977.1|3115726_3116857_+|DUF1624-domain-containing-protein
MINSEISPANSARIRSVDFLRGAIMVLMAIDHVRVYSGMPSGGADPAIFFTRWVTHFCVSGFVFFAGAAAFLYGHKINNPNKLSRYLFTRGLLLVILELTLIRFCWSFNLDFKTFMLAGVIWMLGWCMVLLSGIIRLSFRAVWISGLVIIAAQQLFGLIPASWTWWDFLYPRSEEGPGWIHVLYVLVPWIGVMMAGYGFGKLLIFEPDRRNKLCLQIGLSAIGLFLVAGSIIAASGHKNNLPFILRLLSQQKYPPSQLFLLMTLGPLITLVPLAEKAQGVLARVLNTFGRVPLFYYILHIALIHLLALGLNGILYGSGHQEWYNTAPFTNVPEDYRWGLPLLYAIFITAEVVLYFACRQYSVYKAKHPEKLWLKYL
>NZ_CP042437.1|WP_147053976.1|3111893_3115223_-|hypothetical-protein
MTSAENYELLIEKINIFIRKYYFNNFLRGLIFLGAGLFSAYVIITLSEYFGNFNILFRTILFYFFILLNAALVCWLILPPLLSWLKLGRSLTHDEAAAIIGKHFQDVNDKLLNTLQLKKLAADDEKHRALIEASIDQKIESLKPVSFPSAINIRENVKYLKYILVPAAIILVIGLAAPSVLTESTKRLIRHNEFFVPAAPFKFNILNQTLSVVQGDDLKLDLKLDGDKLPADVYVETANNTFKLDKENISRFHYQFTNLQQNTKFRLIGNGFTSAPYEIKVNQKPALLHFDVALNYPAYLHKKNEILTNAGDLVIPAGTAVKWLLHTQYATGLQFFMNNEPRQAVANGPGLFVHNEKVYKNAVYRLYPVNNQVNHSDSATYHINVILDEPPVISVDEKPDSVSMKSLYFNGKIQDDHGFSALNFHYNVQSSGNKGNTKAFVKRVEADMGQTQADFFYFWNLKDMGINPGDQVTYFFEVADNDGINGPKKARTPERTLHVPDAKEVNQQLNAGTEAIKQKMQSAIKLAGQVEKESQKLNQMLLNKNSLSFDEKKQIEDLLQKRKDLEDLVKEIKDDNKKNLYSRQENQQQNEEILAKQKQIEDLFNNVLDQKTKELLQNLQQLLNEQQKDATRDELSKMQMDNKSLKKELDRMLELYKKLEFDQKLNQQIDELNKLADKQQKLSEQTQKQGADKKQLQQEQDGLKKEFDDVKKGFDDLQKTNEQAEHKSDFQNPEKETQSIAQKMEQSAGDLQKNDKNKASKSQKQAADEMRDLAGKLQQQDQEGESKENAVDAQQLRELLKNLVNSSFSQEKLMQTLKSTSPTDPAYITLSQSQKDIKDNLKTAEDSLYALSRRIPQIQSTVNAEIGSINSRIDQALDNLGDRRTAEANRNQQLAMTSMNNLALMLSEALDQLQKMMNKSKGGKGKPQSISQLNKMQQQLNKNMQKAREQMQQQGNKPGQSQPGQGNMSEQLARMARQQQQIRQQLEQINREENKNGTGKLGNLDKISQEMEQTERDLVNRKITDEALKRQQQIQSRLLEAEKAQQEREQDQQRESQAGKNIPPGYIKALQGYQQQRAKQTEQVKTVSPALNLYYKQKIKSYFDQLNAK
>NZ_CP042437.1|WP_147053975.1|3111469_3111892_-|ATP-binding-protein
MEQANVQTGELFTLQLPSNPESITQLEALIEEIADKYHVADDTFANMMTCLNEAAINAIIHGNKLDAAKKVIINADVAPKRVIWTVTDEGDGFDYNHLADPTAPENLESLTGRGVFIIKHLADQCIFNAKGNEIELHFKI
>NZ_CP042437.1|WP_147053974.1|3111038_3111470_-|rRNA-maturation-RNase-YbeY
MPAISFFEEDINYKLKNKALVRQWIKDTIVAEGFKLKELNYIFCSDAYLLTLNQQYLDHDTYTDIITFDNSEVEGNIVGDIFISIERIRENAIKFGHSETEELHRVIIHGALHLVGYTDKSVVTKKKMTQKEDEYLAKRSFIG
>NZ_CP042437.1|WP_090652238.1|3121914_3122145_-|hypothetical-protein
MGLPLRITYNDTDLVYQVNTSPINKTTSELEILLNGETITLQKDERSVWIQQGNGPLIDPELAQALGRSVSLRFRM
>NZ_CP042437.1|WP_158642896.1|3122276_3122642_-|response-regulator
MAKKILIVDNNELMIEVMTYILTANGYDVVSFHDAGNIFAEIKTSHPDLVILDVLLPGLDSLEICKLIKLNRNTKNLPVIICLPGEDVGTALNQKGAPDDVLLKPFGINNLIEKVEYQLAA
>NZ_CP042437.1|WP_147053985.1|3122846_3123857_+|substrate-binding-domain-containing-protein
MDIVNIKKLAKELNISTSTISRAFNGSPDINKDTKERILAFAKEHNFLPNHYASNLRDKKTKTLAVIIPEIANDFFSQAINGIEEVARKKGFYILLYRTDDVFEKEVSFVNYLNNGKVDGIIMSVSGEANDHNYLRQLESKNVPVVFFDRVYEDIDAAKVTTNDYDSSFDATEHLLQTGCRRIAYLVVNKSISIGQVRMQGYMDALKKHNVVFDDELVIDCSNDEKVNYKILTKVLQEIKPDGIFSSVERLAFATYYVCNDLAIDIPKQLKIVSFSSLGIAPLLSPALSTITQPAYEMGIKAANLLFEALEHKAATNHKRHVVLKSKLFIRRSSGE
>NZ_CP042437.1|WP_147053986.1|3124006_3124636_-|NAD(P)H-dependent-oxidoreductase
MSLIDQLQKRAAVKKFDPSKKISAEQLDQLQSAIQLAPSSLGLQSFKVIVVQDAETRQKLRAAGYNQPQITDSSALFVFASLTSLDEAFGKKFIDLVANVRNVERESLAGYEQMILGKLSSLTDEQKLAWSHKQTYIALGVLVSQASELGIDAAPMEGFDAAKFDEILGLKELGLTTSVIAAVGHRADDDVYSKMIKVRRPKSELFIHV
>NZ_CP042437.1|WP_147053987.1|3124704_3126954_-|penicillin-binding-protein
MKRLNPKYIRIAAFVLIPLFLILLIGGYIAYSKREALLQKAIVKATAKAKRDYNLDVKIGSAHFTGAATVSFSDVTIVPEQRDSLLRIKNFVVSVKLLPLIVGNIKLSDVLLQDGFINLTNIKGVKNFDFLFKKKRDTTSTTKADLAVLANNLVNEVLYKIPDNLTLSNFVVSFKDDSTKLKLLAKTAQIKDGNLTSTIDVDNGESTWHFVGKMHPSDKNIDVKLYADGKKIELPIIQEKLHLKINADTISTKLTKVEHSGGETRIYGSWGVSNLLINHPGLSPGDIIFPRASIDANLFVGSNYVSIDSSSTIHIKNLVARPYIKYTLNPTKIYELKMNTDWLNATDVFDSFPQGMFDALDGIKVAGKLKYSMHFYMDATKIDDLQFDSRLDKDGFRIIKYGKTDLGKLNSPFVYTPYEKGKPQAPHLIGPDNPEFTPLEQIAPNLRNAVMTAEDPSFYTNHGFVEEAFRKSLATDFKTKKFKRGASGISMQLVKNSFLNRDKNLARKIEEILIVWIIENNRIMTKNRMLEVYLNIIEWGRNIYGIDEASHFYFGKSPSELTLGESIYLASIVPYPKGGLYAFQPDGSLRPGLHGYFNLIGKLMAEKGLTARDTSAYGFYNVRLKESLREKIAPIDTAKADSLMKQGGNDDNETLPVIEEPVKKPNFFQRLFGKKDSVEQKKEQVEKQKEKTAKEKLKEQIEALKQDYKNRIDNIDTAGKTRKDIRQEKRRLKKEESDKEDELKAKANL
>NZ_CP042437.1|WP_147060968.1|3127074_3128160_+|P-loop-NTPase
MITKEQVLQALGNVEEPDLKKDLVTLNMIQDIHIDGNKLSFSVILTTPACPLKAMIENACRNAISYFVSKDVVVDINMTSRVTTQKNTGVPGVKNIIAVASGKGGVGKSTVAANLALGLAKSGAKVGLIDADIYGPSVPIMFGLEGARPQAGVVDGKTRIEPIEKYGIKLLSIGFFTDPNQPVPWRGPMVSTAVKQLFNDADWGELDYLVVDLPPGTGDIHITITQTFPVTGAVIVTTPQNVALADARKGVGMFMMPAINVPILGVVENMSYFTPAELPDNKYYIFGKGGGQKLAAQLDVPFLGEIPLVKSISDSGDAGTPAILEADGVMTKAFIDMAQRVAQQVAISNAKAFEARLESEA
>NZ_CP042437.1|WP_147053988.1|3128308_3128587_+|NifU-family-protein
MSLLSQVEAALDTIRPYLEADGGNVSVEEITPEGVVKLKLLGSCGSCPMSIMTLKAGIEQAIKKAVPEITGVEALNLTDIDDPNAVLPENLR
>NZ_CP042437.1|WP_147053989.1|3128702_3129329_+|hypothetical-protein
MKYLVVIFLLFASVAAFAQKHDDRPLVQFTGVVHNADSTDVIVPYVSITNTSFHNQVYLSNYKGYFSFVAHEQDTLRFTCVGYGQILVVIPSNLNTKSYTLQVNIKPQIINLPTFHVFPWATTDEFKKDFLAIKLADDDLEIARKNISKASLSALYNTLPRDAQEIQSANAQSMHNTILNTHSLTPNPLLNPLAWGSLIKQISDADSK
>NZ_CP042437.1|WP_147053990.1|3129449_3130022_-|peptide-deformylase
MKYPIIAYGDPVLRKKATAIEPDEYPHIKELVNNMFETMYGARGVGLAAPQVGMSMRLFVVDATPFDDDEPELKDFKKAFINATIIEETGEEWGFNEGCLSIPDIREDVYRKPVIKISYYDENWKHYEETFKGMAARVIQHEYDHIEGKLFTDKLSPLRKRLIEKKLNDISKGAVNVEYKMKFPAVKKGR
>NZ_CP042437.1|WP_147053991.1|3130042_3131272_-|insulinase-family-protein
MIDYQAHTLPNGIRILYKQSPFAITHCCFIVNAGSRDEANQQEGLAHFIEHLLFKETERRNTNQILNRLELVGADLNAYTTKEYTCIHASLLNQHLERAIDLFEDILFHSTFPEDEQEKERGVILDEIASYLDQPEEAIQDDFEELLFKDDPFGKNILGTPETVGRMNSDDMRAFIKANYSTSEMIFAVHGNYDFKKVVKLCEKYFGGIQAHHPKKNRIAPKANNSGIVVVKKPISQTHCIIGGQAYPSSHQHKYGLLLLNNLLGGMGMSSRLNLEIREKYGIAYTIESNYTPFSDTGIFSVYFGTDSEKAEKASRLVHKELKKLRDQKLGTLQLHQAKQKFIGQIALAEENRMSLIISMAKSLLDFNHIDTLEDIFDKINAVTAEQLLEIGNEIFDNDRLITLKFEPK

Crispr_ID: NZ_CP042437_9

• CRISPR_ID: NZ_CP042437_9
• CRISPR_location: 3261353-3261453
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_9

Consensus_repeat	Method
ACAACAGGCTCTGGTTTTGGCGCTTCTGCTAC	CRISPRCasFinder

spacers of NZ_CP042437_9

>9.1|3261385|37|NZ_CP042437|CRISPRCasFinder
GGCCGGCTTTTCGGCAACAACAGGTTTAGGCGCTTCC

CRISPR arrays and Neighbor proteins around NZ_CP042437_9

CRISPR arrays

The CRISPR arrays of NZ_CP042437_9

>merge|NZ_CP042437|9|3261353-3261453|CRISPRCasFinder
ACAACAGGCTCTGGTTTTGGCGCTTCTGCTACGGCCGGCTTTTCGGCAACAACAGGTTTAGGCGCTTCCACAACCGGCTCTGGTTTTGGCGCTTCTGCTAC

>NZ_CP042437|9|9|3261353-3261453|CRISPRCasFinder
ACAACAGGCTCTGGTTTTGGCGCTTCTGCTAC	GGCCGGCTTTTCGGCAACAACAGGTTTAGGCGCTTCC
ACAACCGGCTCTGGTTTTGGCGCTTCTGCTAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_158642899.1|3253159_3254305_-|DUF4249-family-protein	unknown	unknown	gnl|CDD|379442
NZ_CP042437.1|WP_147054179.1|3266850_3267372_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|224584
NZ_CP042437.1|WP_147054175.1|3263815_3264217_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147054156.1|3250827_3251997_-|DUF4249-family-protein	unknown	unknown	gnl|CDD|379442
NZ_CP042437.1|WP_147054152.1|3247180_3249565_-|hypothetical-protein	unknown	unknown	gnl|CDD|376626
NZ_CP042437.1|WP_147054189.1|3274281_3274920_-|GTP-cyclohydrolase-I-FolE	unknown	unknown	gnl|CDD|236472
NZ_CP042437.1|WP_147054185.1|3269504_3273239_-|GHKL-domain-containing-protein	unknown	unknown	gnl|CDD|227333
NZ_CP042437.1|WP_147054162.1|3254331_3257109_-|TonB-dependent-receptor-plug-domain-containing-protein	unknown	unknown	gnl|CDD|238657
NZ_CP042437.1|WP_147054148.1|3244863_3245364_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_158642898.1|3251999_3253160_-|DUF4249-family-protein	unknown	unknown	gnl|CDD|379442
NZ_CP042437.1|WP_147054166.1|3258123_3258735_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147054150.1|3245429_3246650_-|tyrosine-type-recombinase/integrase	unknown	unknown	gnl|CDD|271185
NZ_CP042437.1|WP_147054164.1|3257197_3257944_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147054154.1|3249638_3250826_-|DUF4249-family-protein	unknown	unknown	gnl|CDD|379442
NZ_CP042437.1|WP_147054172.1|3263225_3263690_-|ribosome-assembly-cofactor-RimP	unknown	unknown	gnl|CDD|179358
NZ_CP042437.1|WP_147054183.1|3268794_3269328_+|putative-metal-dependent-hydrolase	unknown	unknown	gnl|CDD|183954
NZ_CP042437.1|WP_147054181.1|3267368_3268706_-|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|378963
NZ_CP042437.1|WP_147054187.1|3273303_3274191_-|ACP-S-malonyltransferase	unknown	unknown	gnl|CDD|223408
NZ_CP042437.1|WP_147054177.1|3264396_3266760_-|prolyl-oligopeptidase-family-serine-peptidase	unknown	unknown	gnl|CDD|224423
NZ_CP042437.1|WP_147054170.1|3261986_3263222_-|transcription-termination/antitermination-protein-NusA	unknown	unknown	gnl|CDD|236410

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_158642899.1|3253159_3254305_-|DUF4249-family-protein	gnl|CDD|379442	pfam14054, DUF4249, Domain of unknown function (DUF4249). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 279 and 365 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	1.52907e-41
NZ_CP042437.1|WP_147054179.1|3266850_3267372_+|GNAT-family-N-acetyltransferase	gnl|CDD|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	1.42051e-29
NZ_CP042437.1|WP_147054156.1|3250827_3251997_-|DUF4249-family-protein	gnl|CDD|379442	pfam14054, DUF4249, Domain of unknown function (DUF4249). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 279 and 365 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	1.24793e-42
NZ_CP042437.1|WP_147054152.1|3247180_3249565_-|hypothetical-protein	gnl|CDD|376626	pfam01835, A2M_N, MG2 domain. This is the MG2 (macroglobulin) domain of alpha-2-macroglobulin.	2.49549e-06
NZ_CP042437.1|WP_147054189.1|3274281_3274920_-|GTP-cyclohydrolase-I-FolE	gnl|CDD|236472	PRK09347, folE, GTP cyclohydrolase I; Provisional.	5.2865e-107
NZ_CP042437.1|WP_147054185.1|3269504_3273239_-|GHKL-domain-containing-protein	gnl|CDD|227333	COG5000, NtrY, Signal transduction histidine kinase involved in nitrogen fixation and metabolism regulation [Signal transduction mechanisms].	7.55103e-45
NZ_CP042437.1|WP_147054162.1|3254331_3257109_-|TonB-dependent-receptor-plug-domain-containing-protein	gnl|CDD|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	1.01959e-21
NZ_CP042437.1|WP_147054172.1|3263225_3263690_-|ribosome-assembly-cofactor-RimP	gnl|CDD|179358	PRK02001, PRK02001, ribosome assembly cofactor RimP.	1.13597e-42
NZ_CP042437.1|WP_158642898.1|3251999_3253160_-|DUF4249-family-protein	gnl|CDD|379442	pfam14054, DUF4249, Domain of unknown function (DUF4249). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 279 and 365 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	2.13606e-37
NZ_CP042437.1|WP_147054154.1|3249638_3250826_-|DUF4249-family-protein	gnl|CDD|379442	pfam14054, DUF4249, Domain of unknown function (DUF4249). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 279 and 365 amino acids in length. There are two completely conserved residues (C and G) that may be functionally important.	2.61986e-38
NZ_CP042437.1|WP_147054183.1|3268794_3269328_+|putative-metal-dependent-hydrolase	gnl|CDD|183954	PRK13291, PRK13291, putative metal-dependent hydrolase.	1.70835e-88
NZ_CP042437.1|WP_147054150.1|3245429_3246650_-|tyrosine-type-recombinase/integrase	gnl|CDD|271185	cd01185, INTN1_C_like, Integrase IntN1 of Bacteroides mobilizable transposon NBU1 and similar proteins, C-terminal catalytic domain. IntN1 is a tyrosine recombinase for the integration and excision of Bacteroides mobilizable transposon NBU1 from the host chromosome. IntN1 does not require strict homology between the recombining sites seen with other tyrosine recombinases. This family belongs to the superfamily of DNA breaking-rejoining enzymes, which share the same fold in their catalytic domain and the overall reaction mechanism. The catalytic domain contains six conserved active site residues. Their overall reaction mechanism involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA.	6.01138e-59
NZ_CP042437.1|WP_147054181.1|3267368_3268706_-|FAD-dependent-oxidoreductase	gnl|CDD|378963	pfam12831, FAD_oxidored, FAD dependent oxidoreductase. This family of proteins contains FAD dependent oxidoreductases and related proteins.	1.1016e-19
NZ_CP042437.1|WP_147054187.1|3273303_3274191_-|ACP-S-malonyltransferase	gnl|CDD|223408	COG0331, FabD, (acyl-carrier-protein) S-malonyltransferase [Lipid metabolism].	4.4027e-116
NZ_CP042437.1|WP_147054177.1|3264396_3266760_-|prolyl-oligopeptidase-family-serine-peptidase	gnl|CDD|224423	COG1506, DAP2, Dipeptidyl aminopeptidases/acylaminoacyl-peptidases [Amino acid transport and metabolism].	5.29993e-63
NZ_CP042437.1|WP_147054170.1|3261986_3263222_-|transcription-termination/antitermination-protein-NusA	gnl|CDD|236410	PRK09202, nusA, transcription elongation factor NusA; Validated.	3.16394e-166

Protein sequences

>NZ_CP042437.1|WP_147054166.1|3258123_3258735_+|hypothetical-protein
MNDGYHNIPEQTEGGMTDFIHFADLDTREEAHNLFLLAKNRLKDISNWHQFAGPASSKFSLTDAQGNELYRMAEKGDHFYVDLPAPGSIAGGGLDWVMIESIREFENAGSESEFIAITVRPVANPRNPGEAIANFYDHSATNTFIVERYLNHVSAAVHGRNEVINNSDTNLYDSIRNTIIALTARKGLSGPQWKALVEGLLKD
>NZ_CP042437.1|WP_147054164.1|3257197_3257944_-|hypothetical-protein
MINKPFLCFFIVFTYISGRAFGQTVTDDSTMQKIAIGHVVDAYNTSIGQMSRLYNGPEYEFYDPLIKGNACFLDVNAFKTGSVNYDGIFYANVPMMYDINKDLVVTLLYNGFSKYSLINSRLQSFDLLSHHFVYVAADSTNQASSISSGLYEEIYGGNLQVLVKWTKSIQSISTQTTLETFFTEAKKHYYLKKGNNYYSTGGQGAFLNALKDKKKELQQYIKANKISFKDNPEKAMYLIAAQYDQLSK
>NZ_CP042437.1|WP_147054162.1|3254331_3257109_-|TonB-dependent-receptor-plug-domain-containing-protein
MKKIYFFTFCFLILMKVGNAQQTAVKTISVNVQQATIEQFVTEIEAKTGYHFYYEPALFDSLKVTVKLDNKPVNAVLDAALKNTVFRYAITAEGQVFLTKGREIQPSLAAGFFGIKQGPETVKNNVTTTVAEFTDQKEKIIPEATTENKLYEIGNKTNTIGTGNATLSGYVRDSKSGEAVIGGSIFVTNTKTGVATDQFGYFTISLPKGRQILSIRGLGMRDTRRQIVLYSDGKLIIEMKEQVTSLKEVKISAEKVANVRNVQLGVNRLDIKSIKQVPTVFGEADVLRVVLTLPGVQSVGEATTGFNVRGGSADQNLILMNDATIYNPSHFFGFFSSFNPDIVKDIELYKSSIPEKFGGRLSSVLDVTNREGNKKKFTGSAGIGLITSRLNVEGPIIKDKTSFSFGGRTTYSDWLLKLLPEAYKHSQASFYDLNLDISHQINEKNNIYVTTYLSKDKFKLNSDTSYGYSNRNANIKWKHNFNDKLFSVIGAGVDRYQYDIASYDNPVNAYKLNFDINQTNFKADFTYYLNRKNTIDFGLSSIFYKLHPGNFQPNNPKSLVAPDVIPAQQALESALYLGDKYDFTEDFSVSGGIRYSIYNFLGPQLVYNYAPNLPKTTSNLLDSTNYSSGKFIKTYSGPEIRLSARYQLGDNTSLKGGYNTLRQYIHLLSNTTAIAPTDVWQLSDPNIKPQYGDQVSLGLYHNMKANTIETSVEIYYKRLRDYLDYRSGANLVLNHHIENDVLGTEGKAYGIEFLLKKTTGKANGWISYTYSRTFLRQTNPNEGELINGGAYYPANFDKPHDFNFIGNYRFSHRFSVSLNLTYSTGRPITLPVAKYEYGGSERVYYSDRNQYRIPDYFRSDFSMNIEGNHKVHQLTHNSFTIGVYNLTGRQNAYSTYFTEQGGVISGYKLSIFARPIPFINYNIRF
>NZ_CP042437.1|WP_158642899.1|3253159_3254305_-|DUF4249-family-protein
MVYLILLTATTPACRKPYAPNPVSAPGSYLVVEGVIDPGADSTIITVSNSVHLSDTTSLATETSARLTVESEAGASYSLNEFKAGRYLAIGLNLDKTKKYRLHIRTSGGQEYASDYVPVKPTPPIDSVTYKVTSSGLQINSNTHDATNSTRYYRMAYEEAWKFHARFNSGLIVKNGEIVPRREDEMIYYCYRGDKSSNTILASSEKLTQDVIANAPITVVPPSSEKLTIKYSIQVKQYALTKEAYQFWENIRRNTEQLGSIFDAQPSQLKGNIHNVTNPDEPVIGFVSISTTQRKRIFVDNDRVPYTWYVPDDGLCEKLGYLLNNNGENDVELFIIKLHLNPLEAILNPFTGQIIGYKAASVECSDCTLKGKTTAPPYWEF
>NZ_CP042437.1|WP_158642898.1|3251999_3253160_-|DUF4249-family-protein
MIVKNSYIWYFMTTATMMAGCRKPYAPPAVLAPASYLVVEGVIDSGSDSTLITLSRTVNIANKTSLLIDSAAEVAVEREDGASYPLSKFKGRYLVIGLNLDKAKKYRLHIKTGGDEYASDYEPVKLTPPIDSISYKITGAGLQINSNTHDVTNNARYYRWEYEEAWKFHAAVNSGLIVKNGKVTFRDANEMYYYCYAGDRSSNIVLASSEKLLQDVISQNPVTLIPPNSGKLEIKYSIRLKQYALTKGAYAFWENLQKNTEQLGSIFDAQPSQLVGNIHSISNPAEPVIGYVSVTNMQSRRIFISKNVLPDEWNIDLTGCENNAYLFANPNTRQDDVALFILKGGLIPTLSVLDSLGQVIGYRASTVECTDCRVRGNVNAPGFWQN
>NZ_CP042437.1|WP_147054156.1|3250827_3251997_-|DUF4249-family-protein
MKGNKHIWILILTAWCAAGCRKPYAPPVITNNKSYLVVEGNIDSGSDSTIITLSTTVNLNTHDTTTFQSGAQVSVEAEGGVSMPLQEQQYQPGRYYAAALNLDKTKKYRLHIVMPGNEYVSDYEGVKVNPPIDSVNYKIGSKGLQIFSNTHDPANNTRYYRWAYEEAWRFHSAFNSGLVVKNGAIVPRSSDEGIYYCYAGDRSSTIILASSAKLTQDVIFENPVILIPPNSEKLGIKYSILLKQYALTKAGYDFWENIKKNTEQLGSIFDAQPSQLVGNIHSVTHPNETVIGYISVTNMQSKRIYISSSALPASWQPDYKGSCELDSALFQNPNSKQNDVKVLILEGPLIPITTILKDSYVVLGYTASTLDCVDCRLRGKTEAPPFWTE
>NZ_CP042437.1|WP_147054154.1|3249638_3250826_-|DUF4249-family-protein
MNKIKKPSIWCLLILAGIVVIGCKKPYNPSIISTPNHYLVVEGVIDVGDSVTVIKLSETVNLGDNVKTSGLAGYTVNIQDEGGANVAELKEVPGQSGKYASAAVLTLDQTKKYRLHISGNSKEYASDYIAVKKTPPIDSVGFAPKGGNLNIYVNTHDATNNTRYYRWDYAEAWKFHARYESGFIVDPDTKAIRTRRQNEAMYYCYTGDTSSNTVIASSAKLSSDVIFQTPIIQIPSTAEKLSIRYSILLNQYGLTKEAYEFWENIRKNTEQLGSIFDAQPSQLQGNIHSITNPNEPVIGFITITNIQRKRIFINNSQLPAEWYPVYPYNCSADTALFYNPKTMQHEVQLIIIDGSAIPVSSIVNMNVLIGYTYSTVECTDCRIRGKSLPPPFWKP
>NZ_CP042437.1|WP_147054152.1|3247180_3249565_-|hypothetical-protein
MGKHNRTIKIIISSGLILLLAQTVGFAQVIEQVKNGFNQYRQRSVQEKIYVHTDKSVYLPGEIIWFKTYSVDASFHQLLNLSKVVYVDVIDNAHNAIMQAKIAANYGTGNGSLYIPVSVSNGNYTLRAYTNWMKNFSPDYYFEKNITIVNPLKSPDAPVKETAAAYDLQFFPEGGSLVAGLSSKVAFKVTAPNGNGVAVYRGAVIDQHNDTVARFEPLKFGIGSFTFTPVVNNSYKAIVKTSQGNKLVKELPIVSSQGYVMQLKDNGPDLQVTVNSNTGGGEIFLFAHTRQLVKAALSASLNSGVATFSIDKSKLGEGVSHITIFNNAKQPVCERLYFKRPKQLLQVDAAADQPQYATRKKVNINLGTKGAKGTSVLANLSLSVYRVDSLQQMDADDIFSYLWLRSDLRGNIESAGYYVKNQNAETDAAMDNLMLSQGWRRFQWNNIVNGGSSSFNFLPEYNDHLINAKITNTLTGAPAKDIVAYLSVPGKRVQLYASRSDSSGHLVFNTKQLFGPGEVVAQTNSEKDSTYRIDVLSPFSEQYSKRTIPQLTLTADLQKALEQHSLGMQVQNIYALNKIKRFYDPGVDSSGFFAQPYKTYLLDNYTRFTTMEEVLREYVREDNIVRSKGRYHIKVLNEKGFLDGDPIVLLDDVPVFNIDKVMAIDPLKVRKLEVVRDRYFYGPTVNEGVFSFTTYKGDLGGVEIDPHAVVLDYEGLQLKREFYSPVYDTEKATNSRVPDFRNLLFWSPDVNTNTVGKGQVSFYTSDQKGKYVVSVQGISEEGDVGAQYFSFEVK
>NZ_CP042437.1|WP_147054150.1|3245429_3246650_-|tyrosine-type-recombinase/integrase
MRTNINLLFYLKKRSTYKNGPVAIYLRFTVDGQRAEASTGKTCEPSRWNTQAGRAIGTKEDVRTLNSYLDTLQAKAQDFHRWMTANNEMVTAESLKNRFIGKTGKARTLITVFEDHNQKMRSLVGQEFEKSTFQRYETALMHTKDFMQWQHNVSDIPITKINFEFLNDFEYYLRSVRKCANNSAIKYIKNLGKIVRICLGNGWLTVDPYLNYKPKTKKVHRVVLTKEELTAIAEKQFPVDRLRLVRDIFLFSCYTGLAYVDVKKLKRSEMTKGIDGDLWIHTNRQKTDTLSRIPILPAALKVIEKYEDNPQCIVDDLLLPVMSNQKMNAYLKEIADLCGISKLLTFHIARHTFATTVTLNNGVPIESVAKMMGHTSIKTTQIYAKVMDHKISSDMAALKVKLSAIN
>NZ_CP042437.1|WP_147054148.1|3244863_3245364_-|hypothetical-protein
MIKEINKRVVLVHWKRFAGIDIDVFSSLKGFCDSYPDFNYHTLNNYLSKKKIPFENDDVKIERQPLIQKVTRPNLPPVLFWDFDFDKIDWRRSRLTIMERVLDKGDESDWKELIRFYGHDNVIYALKEEITYLTDMTTDLVCEYFQLSKKELKCYTKKQLNQGHWI
>NZ_CP042437.1|WP_147054170.1|3261986_3263222_-|transcription-termination/antitermination-protein-NusA
MSNINLIDSFQEFKDFKNIDRPTMMSVLEDVFRSMIRKKYGTDENCDVIVNTDNGDLEIWRTRKVMEDGFSEDDDLEVELAEAKLFDPDLEVGDEQIEQITLESFGRRAILAARQTLVSKILELEKDEIFKKYKDRVGEIVTGEVYQVWKKETLVLDDEGNELLLPKTEQIPADYFKKGDSVKAVVHKVDMLNSNPKIIISRTAPEFLQRLFELEVPEIFDGLITIKKIVREPGERAKVAVESYDDRIDPVGACVGMKGSRIHGIVRELKNENIDVINFTNNIQLYIQRALSPAKITSIKLDDEKKTAAVYLKPDQVSLAIGRGGHNIKLAGKLTGYEIDVYREADEHDEDVDIEEFTDEIDSWIIDEFKRIGLDTAKSVLALTVGELVKRTDLEEETVKEVLSILNAEFE
>NZ_CP042437.1|WP_147054172.1|3263225_3263690_-|ribosome-assembly-cofactor-RimP
MNIEKRVRELVEEKIADKPNLFLVDVKMHSNGKLIVLLDGDDGVGIDDCVAVSRHVGFHLEEENVIETAYNLEVSSPGIDFPLSSPRQYAKNVGRTLGIKMADGVKREGILSALTEDAIVIEEKIKEKGKKAETVESVIPLDKITETKVLISFK
>NZ_CP042437.1|WP_147054175.1|3263815_3264217_-|hypothetical-protein
MTLFIIGCSSNQHKINNVKINLTPDKHSLKITGLDPLIVQDINRDSTEGNWQSLVPVYKMPADTDLKNYQPIQPGKYMVADSVVTFTPDTPFAAAQTYFVRYYKYDANSKASDFILGKNKLGSLHYTDLIFKQ
>NZ_CP042437.1|WP_147054177.1|3264396_3266760_-|prolyl-oligopeptidase-family-serine-peptidase
MKKIFTLLLLANTAGAFAQKLDTLTIEKIMRDPKWIGVSPSNIHWSDDSKKILFTWNPDKIGPDELFAATPGGTGPQKVSISDRRGLPAENGSWNKKRTQKVFEKNGDLFLEDLKTGKITQLTHTEERESSPAFNGDESHIIFSQGSNLFYMKLNGNGLEQLTNFVKSKSKKGTDELNEEEKWLKRQQLELFDIVKVEKKEAKQDSTERADLAPKELKELIFGTKRVGRVKISPDERFVTYRLTKSADDVKNAIVPNYVTESGFTEDIPNRSKVGRPSSTSEAFIYDRQRDSVYRIKTSDLPGIKDAPDYLKDYPKEQDAYKKANADRAVTIEGIFWSENSANAVVVISAQDNKDRWIMRLDALTGKLSLLDRQRDEAWIGGPGIENSATGNVGFIDNYHFYFQSEASGYSHIYIVDINSGVKKQITSGKWEVQTLQLSNDKKRFYFTANIDHPGLTDFYSLPVDGGTPTKITGLKGGNDVTLSPDEKWLAIRYSYSNKPWELYVQANKPGARAVQVTRSISAEYESYPWRAPEIITFKNRYGSDVYARLYLPKKVDPAKPAVVFVHGAGYLQNVTYSWSYYFREFMFNNMLADNGYTVLDVDYTASAGYGRDWRTGIYRHMGGKDLTDQVDGVKYLVDKYGVNPKHVGLYGGSYGGFITLMGMFTEPDVFAAGGAIRSVTDWAHYNHEYTSNILNEPFTDETAYRKSSPIYFANGLKGNLLMLHGMIDQNVNYQDIIRLTQKLIELHKENWELASYPVEDHAFEQPSSWTDEYKRIYKLFEQTLKK
>NZ_CP042437.1|WP_147054179.1|3266850_3267372_+|GNAT-family-N-acetyltransferase
MEIKSDGFILRELRLADAESLQKHADNPRIFDALLDRFPSPYTMADAVDFIGLAMAENVQTKFAIVINGEVAGVIGIDLRGDIYRKSALIGYWLGQDHWGKGIMPKAVKLVVNYGFANLDIVRLQAGVLGNNPKSMRVLEKAGFVKEAICKNAIIKNGLIFDEHLYATLKPSA
>NZ_CP042437.1|WP_147054181.1|3267368_3268706_-|FAD-dependent-oxidoreductase
MIKRLFFVLLLLKCPITYAQTIKTDILVIGGGPAGCSAAIQGARSKIKTVLIEAGPQLCPSMQAQTMVTIGHGHNLPSGIWGEFRKWVTVFYKKTPGYDTAYNAPLRLEPYTGAAIIKKMADTVKNLTTKLNTVVIAIKKDGDGWVVTVNQDSKSQQIKAKLIIDATPNASIAEKLNINFKPVDLIADNHQSAAYRTSIATGDGYPEQNGDKTPPSGNYPQLPLYCIPLSSIVAPGAENLLVTGKLFPGDDIQYLPNQLMLGQGAGAAAAFCAFFKTTTHKLNSRTVQGELLDFKSYLVPFADVNQNDRYFRSVQQVAATGLLKGGQKLDSNVPELLFMPDSAVNTAEIEPVLNDIYTRTFLWFNREKPKPKFTVENTLSLISEITLTDPKTLHISMAKAWKSQYKFQSDFDVNRPITRREFAILVNQFLNPFARTVDLSGRFIN
>NZ_CP042437.1|WP_147054183.1|3268794_3269328_+|putative-metal-dependent-hydrolase
MTDEQMKFPIGKFAPPASYTDENIREWVDDLRTLPGKLRNAIAGLNYQELDTPYRTGGWTLRQVIHHLADSHMNSITRFKLALTETNPVIKPYEEADWALLPDYRLPVESSLKILEGIHIHMVALFESFTENEWERTFVHPASGDTVSLKKGLALYSWHSKHHLAHITETVKKFARD
>NZ_CP042437.1|WP_147054185.1|3269504_3273239_-|GHKL-domain-containing-protein
MTTPGKIRVLLTLIGIGLLFTAIFIQKTYTPVNNLDQSALALEANLHKKEAYIGKLLKDKEQVNKFKTLADNDQEAINRIEEFTTKRNTWFITAYNNHLSFWSGIKVLPDSIGNIHEGNSFIRQPNGYYEAIRKTEGAFSVIFFIPVKINYSFTNQYLQNTFAKDLITTDNIELTDLGDKNAYDVHSINNDYLFSVKQKASSVNYAFIYYQAVFWILTIITLCILIHNICCHMAAKGYAWLSVVFLGLYIILFRIVNLYYHLPDFRGMLKLFDPAIFHSGVLYPSFGDLCINLLCVFWFVAFIYLQRRRLFTAVYKNSIGYFIVAGCILLLIGLSTSLLRLFYDLVIHAGINFNVNNVLGLSSFSILGVLMLCFSFLIFYLVDEVVLFICLKLDVPKLHQLLLLVVGVVISTVVFAHHYDFSLFYLLWMLLVVMRAFGFIYQGGKLTTSAFLGVLLICSLISAIKLNHFEGIKEEAVRKKLLQRLGDPIDHYAENAFIKIEKRILVDTTIVRYFKENIHNNEYLLTRFQKLYFDGYLSKYVIKIHEYDASDQPLANDDIPITGFKDQVVYNSYKVVPTSYFYRGTASFGRQSYFAILPIKNGNKQLGTLAIEFTSKPVQVLGAFPDLLIEGSLQSEDEFKDYSYAYYYDNRLQSQRGSYVYTLNNPDFKGVLKSYITKTTRFNNPEWYNTFTKYDHLIYKPNKRNIIVVSKETNPLYNGVASITFFFMALLVFSAIIIIARGVWVRVRILSIKDDKIRWKFRINFDKVLYRTRIQFVMIFAVVVTLIVVGFITFVSIGRQYHEQQDKQIRDKITRIAETFQTGALNRYIYNVNEKNQVDFNVLAETYSTDLILFDTNGVPLVTTQPKMYEAGLVAKKMNSRAFIYLSRLQKTEFVNDEKIGELSYKAAYAPIVSSGQKVIAYIQLPYFSNEADYKQRISSLLNVMINVYALVFIAIGLLAIIIARQITAPLSFIQETLSKTIYGKKNEPIKWQRNDEIGALVKEYNKMISALENSATRLAQSERESAWREMAKQVAHEIKNPLTPLKLGLQLLDKSWRDKDPKFDQKFERFSKSFVEQIESLSSIASEFSAFAKMPDTRIEQLNVFEMLNQAVTIFKQMDNIHIVYQLPEAPFMINADKDQLLRCFNNLLKNAIEATPADRNGLININYLITSKNVLLTIKDNGNGIPENMREKIFEPNFTTKSSGTGLGLAFVKNSIENANGKVWFETTIGVGTTFYLSFPSA
>NZ_CP042437.1|WP_147054187.1|3273303_3274191_-|ACP-S-malonyltransferase
MKAYIFPGQGAQFPGMGKDLYEQSDKAHELFEKANEILGFRITDVMFDGTAEDLVQTNVTQPAIFLHSVILATVLGDDFKPDMVAGHSLGEFSALVAAGALSFEDGLRLVAARANAMQKACELQPSTMAAILGLDDFTVEDICQRATGVVVTANYNCPGQLVISGSIEGIDEACEKLLAAGAKRALKLKVGGAFHSPLMESARVELEAAIVATEIKAPVCPIYQNIDAKPYTDPAVIKQNLIAQLTGAVRWTQTVKHMLEDGATSFTEVGPGNVLQGLVKKVDRAIVTQSAVIPQ
>NZ_CP042437.1|WP_147054189.1|3274281_3274920_-|GTP-cyclohydrolase-I-FolE
MIDKNHIPDRDDDIDGYTKIDRYNPQLIENLSAHYLDVLKQIGENPQREGLLKTPERIAKAMLFLTHGYDLDAKSILNSAMFKEEYSQMVIVKDIEVYSMCEHHMLPFFGKAHIAYIPNGYVVGLSKIPRVVDAFARRLQVQERLTNEIRDCIQETLNPVGVGIVIECRHLCMSMRGVQKQNSVTTTSAFTGEFLKEKTRTEFLNLISSKLS

Crispr_ID: NZ_CP042437_10

• CRISPR_ID: NZ_CP042437_10
• CRISPR_location: 4073789-4073884
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_10

Consensus_repeat	Method
CCCTTCAGAATTTCGCGAAATTTTACCACTCAG	CRISPRCasFinder

spacers of NZ_CP042437_10

>10.1|4073822|30|NZ_CP042437|CRISPRCasFinder
CATGACAACGCTCTTTAGTATGTTATTTCC

CRISPR arrays and Neighbor proteins around NZ_CP042437_10

CRISPR arrays

The CRISPR arrays of NZ_CP042437_10

>merge|NZ_CP042437|10|4073789-4073884|CRISPRCasFinder
CCCTTCAGAATTTCGCGAAATTTTACCACTCAGCATGACAACGCTCTTTAGTATGTTATTTCCCCCTTCACAATTTCGCGAAATTTTACCACTCAG

>NZ_CP042437|10|10|4073789-4073884|CRISPRCasFinder
CCCTTCAGAATTTCGCGAAATTTTACCACTCAG	CATGACAACGCTCTTTAGTATGTTATTTCC
CCCTTCACAATTTCGCGAAATTTTACCACTCAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147055416.1|4081170_4082181_-|bifunctional-oligoribonuclease/PAP-phosphatase-NrnA	unknown	unknown	gnl|CDD|223691
NZ_CP042437.1|WP_147055393.1|4065328_4066609_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|237355
NZ_CP042437.1|WP_147055395.1|4066791_4068270_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147061008.1|4076426_4076954_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP042437.1|WP_147055418.1|4082382_4082802_+|nucleoside-diphosphate-kinase	unknown	unknown	gnl|CDD|184734
NZ_CP042437.1|WP_147061006.1|4070913_4071204_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147061007.1|4075030_4076398_+|MATE-family-efflux-transporter	unknown	unknown	gnl|CDD|240536
NZ_CP042437.1|WP_147055405.1|4074027_4074897_-|LysR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223656
NZ_CP042437.1|WP_147055401.1|4069796_4070513_+|pirin-family-protein	unknown	unknown	gnl|CDD|380375
NZ_CP042437.1|WP_147055403.1|4071493_4073344_+|DNA-topoisomerase-III	unknown	unknown	gnl|CDD|236078
NZ_CP042437.1|WP_147055414.1|4080176_4081169_-|FKBP-type-peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|223619
NZ_CP042437.1|WP_147055387.1|4060934_4061924_+|beta-ketoacyl-ACP-synthase-III	unknown	unknown	gnl|CDD|236475
NZ_CP042437.1|WP_147055412.1|4079139_4080120_-|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|223619
NZ_CP042437.1|WP_147055420.1|4083255_4083546_-|DUF721-domain-containing-protein	unknown	unknown	gnl|CDD|377496
NZ_CP042437.1|WP_147055407.1|4077265_4078288_-|type-I-asparaginase	unknown	unknown	gnl|CDD|199207
NZ_CP042437.1|WP_147055389.1|4062198_4062669_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	unknown	unknown	gnl|CDD|235777
NZ_CP042437.1|WP_147055399.1|4069023_4069608_+|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223736
NZ_CP042437.1|WP_147055391.1|4064185_4065052_+|twin-arginine-translocase-subunit-TatC	unknown	unknown	gnl|CDD|376413
NZ_CP042437.1|WP_147055410.1|4078323_4079091_-|YchF/TatD-family-DNA-exonuclease	unknown	unknown	gnl|CDD|238635
NZ_CP042437.1|WP_147055397.1|4068272_4069001_+|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl|CDD|224054

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147055416.1|4081170_4082181_-|bifunctional-oligoribonuclease/PAP-phosphatase-NrnA	gnl|CDD|223691	COG0618, COG0618, Exopolyphosphatase-related proteins [General function prediction only].	1.05233e-35
NZ_CP042437.1|WP_147055393.1|4065328_4066609_+|AAA-family-ATPase	gnl|CDD|237355	PRK13342, PRK13342, recombination factor protein RarA; Reviewed.	0
NZ_CP042437.1|WP_147055407.1|4077265_4078288_-|type-I-asparaginase	gnl|CDD|199207	cd08963, L-asparaginase_I, Type I (cytosolic) bacterial L-asparaginase. Asparaginases (amidohydrolases, E.C. 3.5.1.1) are enzymes that catalyze the hydrolysis of asparagine to aspartic acid and ammonia. In bacteria, there are two classes of amidohydrolases. This model represents type I L-asparaginases, which are highly specific for asparagine and localized in the cytosol. Type I L-asparaginase acts as a dimer. A conserved threonine residue is thought to supply the nucleophile hydroxy-group that attacks the amide bond. Many bacterial L-asparaginases have both L-asparagine and L-glutamine hydrolysis activities, to a different degree, and some of them are annotated as asparaginase/glutaminase. One example of an enzyme with no L-glutaminase activity is the type I L-asparaginase from Wolinella succinogenes.	6.94068e-118
NZ_CP042437.1|WP_147061008.1|4076426_4076954_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	1.11138e-16
NZ_CP042437.1|WP_147055418.1|4082382_4082802_+|nucleoside-diphosphate-kinase	gnl|CDD|184734	PRK14545, PRK14545, nucleoside diphosphate kinase; Provisional.	8.40005e-74
NZ_CP042437.1|WP_147061007.1|4075030_4076398_+|MATE-family-efflux-transporter	gnl|CDD|240536	cd13131, MATE_NorM_like, Subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins similar to Vibrio cholerae NorM. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. This subfamily includes Vibrio cholerae NorM and functions most likely as a multidrug efflux pump, removing xenobiotics from the interior of the cell. The pump utilizes a cation gradient across the membrane to facilitate the export process. NorM appears to bind monovalent cations in an outward-facing conformation and may subsequently cycle through an inward-facing and outward-facing conformation to capture and release its substrate.	8.27876e-96
NZ_CP042437.1|WP_147055405.1|4074027_4074897_-|LysR-family-transcriptional-regulator	gnl|CDD|223656	COG0583, LysR, Transcriptional regulator [Transcription].	3.27134e-36
NZ_CP042437.1|WP_147055401.1|4069796_4070513_+|pirin-family-protein	gnl|CDD|380375	cd02910, cupin_Yhhw_N, Escherichia coli YhhW and YhaK and related proteins, pirin-like bicupin, N-terminal cupin domain. This family includes the N-terminal cupin domains of YhhW and YhaK, Escherichia coli pirin-like proteins with unknown function. YhhW is structurally similar not only to human pirin but also to quercitin 2,3-dioxygenase (quercitinase). Although the function of YhhW is not completely understood, YhhW and its human ortholog have quercitinase activity and are likely to play an important role in transcription and apoptosis. This N-terminal cupin domain of YhhW has a metal coordination site and is thought to have catalytic activity while the C-terminal cupin-like domain has diverged considerably and has closer alignment with C-terminal pirin. YhaK is found in low abundance in the cytosol of E. coli and is strongly up-regulated by nitroso-glutathione (GSNO). There are major structural differences at the N-terminus of YhaK compared with YhhW; YhaK lacks the canonical cupin metal-binding residues of pirins and may be involved in chloride binding and/or sensing of oxidative stress in enterobacteria. YhaK showed no quercetinase and peroxidase activity; however, reduced YhaK was very sensitive to reactive oxygen species (ROS). Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold.	9.34149e-72
NZ_CP042437.1|WP_147055403.1|4071493_4073344_+|DNA-topoisomerase-III	gnl|CDD|236078	PRK07726, PRK07726, DNA topoisomerase 3.	0
NZ_CP042437.1|WP_147055414.1|4080176_4081169_-|FKBP-type-peptidylprolyl-isomerase	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	5.30753e-34
NZ_CP042437.1|WP_147055387.1|4060934_4061924_+|beta-ketoacyl-ACP-synthase-III	gnl|CDD|236475	PRK09352, PRK09352, beta-ketoacyl-ACP synthase 3.	8.82151e-180
NZ_CP042437.1|WP_147055412.1|4079139_4080120_-|peptidylprolyl-isomerase	gnl|CDD|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	1.79566e-35
NZ_CP042437.1|WP_147055420.1|4083255_4083546_-|DUF721-domain-containing-protein	gnl|CDD|377496	pfam05258, DUF721, Protein of unknown function (DUF721). This family contains several actinomycete proteins of unknown function.	1.12186e-17
NZ_CP042437.1|WP_147055389.1|4062198_4062669_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	gnl|CDD|235777	PRK06302, PRK06302, acetyl-CoA carboxylase biotin carboxyl carrier protein.	6.5146e-55
NZ_CP042437.1|WP_147055399.1|4069023_4069608_+|Crp/Fnr-family-transcriptional-regulator	gnl|CDD|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	5.87229e-16
NZ_CP042437.1|WP_147055391.1|4064185_4065052_+|twin-arginine-translocase-subunit-TatC	gnl|CDD|376413	pfam00902, TatC, Sec-independent protein translocase protein (TatC). The bacterial Tat system has a remarkable ability to transport folded proteins even enzyme complexes across the cytoplasmic membrane. It is structurally and mechanistically similar to the Delta pH-driven thylakoidal protein import pathway. A functional Tat system or Delta pH-dependent pathway requires three integral membrane proteins: TatA/Tha4, TatB/Hcf106 and TatC/cpTatC. The TatC protein is essential for the function of both pathways. It might be involved in twin-arginine signal peptide recognition, protein translocation and proton translocation. Sequence analysis predicts that TatC contains six transmembrane helices (TMHs), and experimental data confirmed that N- and C-termini of TatC or cpTatC are exposed to the cytoplasmic or stromal face of the membrane. The cytoplasmic N-terminus and the first cytoplasmic loop region of the Escherichia coli TatC protein are essential for protein export. At least two TatC molecules co-exist within each Tat translocon.	7.64477e-73
NZ_CP042437.1|WP_147055410.1|4078323_4079091_-|YchF/TatD-family-DNA-exonuclease	gnl|CDD|238635	cd01310, TatD_DNAse, TatD like proteins; E.coli TatD is a cytoplasmic protein, shown to have magnesium dependent DNase activity.	2.53975e-96
NZ_CP042437.1|WP_147055397.1|4068272_4069001_+|ATP-binding-cassette-domain-containing-protein	gnl|CDD|224054	COG1131, CcmA, ABC-type multidrug transport system, ATPase component [Defense mechanisms].	4.26375e-54

Protein sequences

>NZ_CP042437.1|WP_147055403.1|4071493_4073344_+|DNA-topoisomerase-III
MKVIIAEKPSVAREIAKVFGATTKKDGYMEGKGYTFTWAFGHLLQLAAPQEYGYYGWSVQNLPMLPPKFKLSIRKVKSKDGMIDDPSVKKQLDIIKSLFDEATEIIVATDAGREGELIFRYIYYYLKCKKPFKRLWISSQTDEAIKEGFRNLKPGSDYDTLFNSAHCRSQSDWLVGMNATQALSLSSGNRGVLSLGRVQTPTLAMICSRYLDNKNFVPQLYYQVSIQPDKDGQVFKAISVNNFKTKEEAQVIFDKVEDVASGFPQGAHIINLEAKPRKEPPPLLHDLSSLQQEANKRKGFTADQTLNILQNLYEGKLVTYPRTGSRYIGDDVFAGVPDLIEKLKEHPDFGKQATLLSGAKLSKRSVNAKKVTDHHAILTTGEPPYQLTPDKQAVYDMVAGRMLESFHQDCIKEITKITVESGSLFMASGTVIQTPGWRAVFNETDDEKKDEENPTLPKVQQGEKLPITDKALLEKQTKPKPLYNEASLLKALETAGKEIDDEELRYAMKDSGLGTPATRASIIETLLKRNYILREKKNLVPTPTGLAVYQVVKNQQIAQAELTGNWEKRLEEIRTGASVADFQEEIKTYTRAITQELLREGKALKIEPAGAGVAVS
>NZ_CP042437.1|WP_147061006.1|4070913_4071204_+|hypothetical-protein
MPILVIGRHPEILATVVRLVNNNPAWNATGCQTDDEAIQAFDAQGFTLVLLGGGIPPESESRLSQYFRDCKPDIRIVQHYGGGSGLLAAEIYEALK
>NZ_CP042437.1|WP_147055401.1|4069796_4070513_+|pirin-family-protein
MAQTVLHKAETRGHANHGWLNSYHSFSFGSYYNPERMNFGALRVLNDDTVDAGMGFGKHPHDNMEIISIPLEGNLEHEDSMNNVAVIKNGDIQAMSAGTGIYHSEYNQDPDKRVKFLQIWIYPNQRNVEPRYDQLTLNLDDRHNKLQQVLSPNPDDTGVWIHQDAWFNLGKFDAGVSTDYTIHKPGNGVYAFVLSGEVQIDGQAVGTRDALGIWDTEGFTITASTDAEFLLMEVPMSF
>NZ_CP042437.1|WP_147055399.1|4069023_4069608_+|Crp/Fnr-family-transcriptional-regulator
MSFTLILNNIAKHIHLTADEQTIFTGMLRPQTIKRKQFWLSDGDICKHSAFVTSGCLRGFTVDKNGIEHVLSFAPVDWWMADMYSLISQKPGMLNVEALEDTEVLLLSKINQEALYKQIPKFEHFFRVLVENSLVASQQRLIDGLSLTAEDRYNNFCKRYPTLIYTLPQKQIASYIGVTPEFFSRMRKKVVRST
>NZ_CP042437.1|WP_147055397.1|4068272_4069001_+|ATP-binding-cassette-domain-containing-protein
MIEIKNLKKIYNGVTVVDVPHLIINKGESVGLVGNNGAGKTTLFRMILDLIRPETGEVLSNGEVVAGHENWKNYTASYLDEGFLIDYLTPEEYLYFIGGLHQQSKATVDETLVKLSDFFNGEILKKGKYIRDLSKGNQCKVGVASCVLQKPELLMLDEPFANIDPSTQFRLKNMLKELNRSQNVTNIVSSHDLNHITDVCDRILLMEKGVIIKDIATSSSTLKELENYFGVGQEAGELTKDI
>NZ_CP042437.1|WP_147055395.1|4066791_4068270_+|hypothetical-protein
MVTSFISHELKAFWRSKNTGKSIAIRVVMGLLILYLFINVLAAGFFLDKILEQLYPNEELVIPFCGIILIYFLFDLLMRLQFQELPTLRVQPYLHLPITRNFLVKYLALSASLSVFNLWPFVLFLPFVFKVIAPDSGAIIVLAFVVSIAGFTVFNNYLALYLKRKSNINGWVFLISAAVLALIITGDYLWHIISLRAISYAFFGKLLTMPAMVLLPVILGLAMYYLNFLYLKQNLYLEDLTAHKVSSYKSSTDIPFLSRFGSVGDLAANEIKLVLRNKRSRSALVMGLFFMFYGLIFYSNSHYHGDGYKVFAGMFMTGIFIINYGQFMFGWQASHFDGLLVNKISFADFIKAKYLLFTTISTVFFILTTPYVYFGWRVLITHFIMYLWNIGVNTTMVLYFANRNFKRLDLSKGAAFNWEGVGATQWILSLPLMITPFVIYGPFALLKHPNIGLALIAAIGLAGVLTRNYWVKVLETDYRTKRYQIAEGFRNK
>NZ_CP042437.1|WP_147055393.1|4065328_4066609_+|AAA-family-ATPase
MTNLPPLAERMRPKSLDDYVGQKHLVGPGAVLRKAIESGALPSMLFWGPPGVGKTTLAYIISQSLNRPFFALSAINSGVKDVREVIEKASLLKQGGQTLPILFIDEIHRFSKSQQDSLLGAVERGIVTLIGATTENPSFEVISALLSRCQVYILQPLAEEDLLNLLEKSMQEDVVLKEKHIIIQDHEAIMRLSGGDARKLLNIFELLVNAFDSADIVLTDEVVLEHVQQNMALYDKTGEQHYDIISAFIKSMRGSDPNGAVYWLARMIAGGEDPLFIARRMLILSSEDIGNANPNALLLAQSCFEAVNKIGMPESQLILSQTAIYLATSPKSNSATTAIGAAMALVKQTGDLPVPLHLRNAPTKFMKNIGYGKDYKYAHSYEGNFTDLDFLPDAIRGTKIYEPGNNARENESKEKLKKLWGDRYKY
>NZ_CP042437.1|WP_147055391.1|4064185_4065052_+|twin-arginine-translocase-subunit-TatC
MSDNKLIKAIKDKGKTMEAEMSFFDHLEALRWHLIRSALAIVVITSFVFYFYDWIFDTIIMGPSKPTFWTYRMLCALGDLLHRPGFCIDKINIQLINTEMAGQFTLQINSSLIIGLTLGFPYLLFEIWRFVRPALHEKERKAASGFVFYATALFIIGVLFGYYVITPESINFLSGYTVSATIKNLFDIDSYLSSVSTLTLATGIVFELPILVYILSNLGILTAKFMRETRRYAIIVIMVVAAVVTPTPDMMTMTVVSIPLFALYEVGILVSAVVEKRKLKRAQEDGLV
>NZ_CP042437.1|WP_147055389.1|4062198_4062669_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein
MDIKQIQDLIRFVSKSGVNEVSIEQKDFKITIKTNETQPQVIHASIPAQTAPVVLPPAPVAAEPVAPAAPAGPDTSKYLTIKSPMIGTFYRSASPDKPLFVNIGDEIKTGSVVCIIEAMKLFNEIESEISGRIVKVLVDNASPVEYDQPLFLVEPV
>NZ_CP042437.1|WP_147055387.1|4060934_4061924_+|beta-ketoacyl-ACP-synthase-III
MSKIHAAITAVHGYVPDYVLTNQELETLVDTNDEWIVSRTGIKERRILKGEGLGTSDMAVPAVQALLKKRGIGAEEIDLIIFCTTTPDYVFPATANILANKIGAKNAWGYDLSAACSGFIFGLATGSQFIESGKHQKVLVVGGDKMSSIVNYQDRATCIIFGDGCGAVLLEPNFEGNGVMDSILKSDGAGVTYLHQKAGGSVRPASHETVDNHEHFAYQEGQAVFKFAVTNMADVAHEVMERNGLTGEDVAWLVPHQANKRIIDATARRTGLSDDKVIINIERYGNTTNGTIPLCLWEWESKFKKGDTLILAAFGGGFTWGSIYLRWAY
>NZ_CP042437.1|WP_147055405.1|4074027_4074897_-|LysR-family-transcriptional-regulator
MDLQQIKNFLALADELHFWNTSAKQNITQSALSRQIKSLEDELDVQLFERTKRSVKLTPAGEFLKTKWAGIVDEFNFIHQFAKKIELGETGSIRIAHPDSISFSTLPQLILDISIRYPELKIEMIQLAYEDEQEFLTKYKIDLKFSRDINRLDNISTMKVQTDHLALVLPQEHAFKELADITAKSLQTQKFIMPRSNSSSSYSQLTRQVFEHYGISPESFYTSDFGSTIISLITRQFGISIMPYSYANQGYQGIRFIELPFESNLFVHWRTDDHSPILKNILRMVEGLA
>NZ_CP042437.1|WP_147061007.1|4075030_4076398_+|MATE-family-efflux-transporter
MRLAYPVMISQVGHPLVGFSASIILGHFAGTVPLAALAIANGFFNLMLIIAIGISYGITPLVARENGAGNYRECGRLLWHSVVVNILTGLMLLIITWFGGQYLIAHIGLDAAVVAQAKPLLVLLGLSIIPLMLFLSFKQFAEGLGFTRLAMQVSIWGNVINIVVGIILVKGLFGMPAMGAKSIGYSAIIDRGLMAVVMATFVLKKHRFNKFLQGCRPFQFNVGRFKKILATSVPIVLQNIFEISAFSAAVFIVGIIGARQLAAYQIAMNYLSFIYYAVNGIGTAAAIQTGYFLGQAKFYLLRVSALASYHLTIIFHLVTGGLLLVLKSVLPKVISVDLQVVSMVGNLFIIAAGLEVFDGLQVVSLGILRGLGDLKYPVLINLAAYWGVALPVAFALGLHTPMGLTGVWLGLYSGLLVASALLYLRFRHLVNAKYFADNVPAAQEHLFNNVVQLES
>NZ_CP042437.1|WP_147061008.1|4076426_4076954_+|GNAT-family-N-acetyltransferase
MNSAGIRFIKVDMQNIQTLKAIGIETFNEAFAHLNTPENMEDYLATAFANEKLAGEVNNPNSEFYMAQIDGNIVGYVKINHGPAQTDVKDDDALEVERIYVLKAFHGKKVGQLLFDKALDIAAQMKKTYIWLGVWEHNAKALAFYKKNGFEVFGSHPFWLGDDLQTDLMMKRYLD
>NZ_CP042437.1|WP_147055407.1|4077265_4078288_-|type-I-asparaginase
MSQILIIYTGGTIGMMSDPVTKVLKPINFEQIMDNVPELEKLNCRIKVHSFDEIIDSSNMNPAIWSDLAGLIESNYHDNDGFVILHGSDTMAYTASALSFMLENLGKPVIFTGSQLPISAIRTDAKENLMTAIEIAKAKKNDRARVPEVCIYFDYKLFRGNRAFKYNSSKFEAFRSPNYPILAESGVHLKFSVNDIRHPQDGENLIIHNNLISDVGVLKLYPGIGTKVVEAILNADVRGVVMETFGAGNTTTDAWFISLLEKAIKDGKVIVDISQCKVGTVELGRYETSKQLKDMGVANGYDMTFESAVTKMMYLLGKFDDPALVKHYMETDLRGEITVS
>NZ_CP042437.1|WP_147055410.1|4078323_4079091_-|YchF/TatD-family-DNA-exonuclease
MVLTDTHTHLYYETIPVKRAALVQRCIDNDISRLFLPNVDAASVPLVYDLLQAYPGLCYPMLGLHPCSVKADWEQELAAIKAAQGQHPIYAIGEIGIDLYWDKAFLTEQVKAFKQQINWAKSLDLPIVIHCRDAYDEVYEVLQQENDDKLRGIFHCFGGTVEQAQQVIDLGFHLGIGGVVTYKNSGLDKVVAEIDLNHIVLETDSPYLTPVPFRGKPNESSYLIYIAQKVADLHQTSVEEVARVTTENSRLIFGI
>NZ_CP042437.1|WP_147055412.1|4079139_4080120_-|peptidylprolyl-isomerase
MKNIFYLLTALFGIATLTAHAQTGMQTTPAGAQYQIFTHNTGEKIKLNDIVYFNYIQMTDKDSVLYSSFKTGKPQPAQIRPSQNVADLMDIFPLLALNDSAMVKVPTDSIFKGHEEARPPFFPKGSKLVFILKIIKVQSLQEAMAERTAAIEKMKSQEATETNTYVTANKLSPVTTASGLKYIITKASALRKPLDGDTVMVNYTGYLLNGQLFDTSVQANAKAAGVEQPGRPYEPIPVVLGAHAVIPGWEEGLALLHEGSKAKFIIPSKLGYGEQGMGNGAIPPYATLVFDVEIVKVKPGKHVPVAARPGVKHTVRKKTTVAKKKN
>NZ_CP042437.1|WP_147055414.1|4080176_4081169_-|FKBP-type-peptidylprolyl-isomerase
MKQKLMFLAIAAIGFSSCNGGFKKGDAGLLYNIHTSKGGTHIKDGDFVSVNMIVKTDGDSVLSNTYDMGHPIIIMPMPKPQAKGDIYAGLELLGEGDSATFKVPTDSIFKGGQQRPPNLKGKFLIFQVNVNKVLAKGSLTEQVFRGRVQDYLKTLTEAMKAQEPGKIKKYIADHNLKVTTTASGLNYVITTPGTGPTPAVGDTAVVNYTGRLPNGKIFETSVKEVAIKEKQPIEPGRPFAPLRIPVGQGKVIPGWDEGLQLMNKGSKITLVIPSAIAYRDQGVGPIGPFTPIIFEMEMVEIVKPNPNAPKPVMPQMQMQQAPSQSQPTQR
>NZ_CP042437.1|WP_147055416.1|4081170_4082181_-|bifunctional-oligoribonuclease/PAP-phosphatase-NrnA
MLDLAALTELLASPRKIVITTHHKPDGDAMGSSLGLYNYLIQQGHHATVIAPTDYPAFLSWLPRNGDVVIYTEQAEKSAALIADAELIFCLDFNALSRINEMGVLVGESKAYKIMIDHHLEPQDFDDYRHWNINACATAQLIYDFIVNELHHRELINADVATCLYTGIMTDSASFRLPNTTSTVHRIVADLIDLGAVNWRIHELVYNSATENRLRFLGHCLANCLEVLPEYHTAIIAVNNTDLHKYDVDTGDTEGIVNYALSMADIKLAAFIVERSDRVKLSLRSKGEFPANEICKKYFDGGGHRNAAGGHSSNTLEQVVQQFKTILPEYKKLLNQ
>NZ_CP042437.1|WP_147055418.1|4082382_4082802_+|nucleoside-diphosphate-kinase
MTTNRTFTMIKPDAVANGHIGAIIDKITKSGFKIIALKYTALSAEKAGQFYEVHKERPFYNALVTFMSSGPIVAAILEKDNAIEDFRKLIGATDPAKAEEGTIRNLFAKSIDANAVHGSDSDENAAIEGSFFFSAFEKF
>NZ_CP042437.1|WP_147055420.1|4083255_4083546_-|DUF721-domain-containing-protein
MRKTNDKSLKEAIEQMLNVYKIKRRYDETGVVAAWPELVGKSVANRTKELFIRDKKLFLRIESSVIKHELMLMRSQIIDKINAEAKGVLVEEIVFL

Crispr_ID: NZ_CP042437_11

• CRISPR_ID: NZ_CP042437_11
• CRISPR_location: 5589976-5590110
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP042437_11

Consensus_repeat	Method
TTATAAAAATAGATAATCAGCCACAAC	CRISPRCasFinder

spacers of NZ_CP042437_11

>11.1|5590003|27|NZ_CP042437|CRISPRCasFinder
TATACAAATATACACACTTGTGGCTGA
>11.2|5590057|27|NZ_CP042437|CRISPRCasFinder
CATGATTTTTGTTGTACTTATGGCTAA

CRISPR arrays and Neighbor proteins around NZ_CP042437_11

CRISPR arrays

The CRISPR arrays of NZ_CP042437_11

>merge|NZ_CP042437|11|5589976-5590110|CRISPRCasFinder
TTATAAAAATAGATAATCAGCCACAACTATACAAATATACACACTTGTGGCTGATTATAAAAATAGATAACCAGCCACAACCATGATTTTTGTTGTACTTATGGCTAATTATAATTTATTATAATCAGCCATAAG

>NZ_CP042437|11|11|5589976-5590110|CRISPRCasFinder
TTATAAAAATAGATAATCAGCCACAAC	TATACAAATATACACACTTGTGGCTGA
TTATAAAAATAGATAACCAGCCACAAC	CATGATTTTTGTTGTACTTATGGCTAA
TTATAATTTATTATAATCAGCCATAAG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147057632.1|5580933_5582031_+|cellulase-family-glycosylhydrolase	unknown	unknown	gnl|CDD|367210
NZ_CP042437.1|WP_147057654.1|5600908_5601847_+|dihydrodipicolinate-synthase-family-protein	unknown	unknown	gnl|CDD|188630
NZ_CP042437.1|WP_147057652.1|5598405_5600640_+|glycoside-hydrolase-family-2	unknown	unknown	gnl|CDD|225789
NZ_CP042437.1|WP_147057642.1|5590524_5590707_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147057639.1|5588479_5589913_-|AAA-family-ATPase	unknown	unknown	gnl|CDD|376582
NZ_CP042437.1|WP_147057624.1|5574059_5575571_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	unknown	unknown	gnl|CDD|369630
NZ_CP042437.1|WP_147057634.1|5582072_5582951_+|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|380381
NZ_CP042437.1|WP_147061068.1|5591479_5592652_+|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl|CDD|349902
NZ_CP042437.1|WP_147057656.1|5601921_5602923_+|4-hydroxyproline-epimerase	unknown	unknown	gnl|CDD|184428
NZ_CP042437.1|WP_147057650.1|5596905_5598252_+|deoxyguanosinetriphosphate-triphosphohydrolase	unknown	unknown	gnl|CDD|234897
NZ_CP042437.1|WP_147057628.1|5578130_5579624_-|TonB-dependent-receptor	unknown	unknown	unknown
NZ_CP042437.1|WP_147061069.1|5590994_5591465_+|GNAT-family-N-acetyltransferase	unknown	unknown	gnl|CDD|366181
NZ_CP042437.1|WP_147061067.1|5585573_5586557_+|type-IX-secretion-system-membrane-protein-PorP/SprF	unknown	unknown	gnl|CDD|274625
NZ_CP042437.1|WP_147057636.1|5583042_5585574_+|T9SS-type-B-sorting-domain-containing-protein	unknown	unknown	gnl|CDD|372639
NZ_CP042437.1|WP_147057638.1|5586561_5588325_+|OmpA-family-protein	unknown	unknown	gnl|CDD|143586
NZ_CP042437.1|WP_147057646.1|5594586_5595984_+|outer-membrane-beta-barrel-protein	unknown	unknown	gnl|CDD|369446
NZ_CP042437.1|WP_147057644.1|5592626_5593967_+|response-regulator	unknown	unknown	gnl|CDD|225114
NZ_CP042437.1|WP_147057648.1|5596125_5596728_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147057626.1|5575627_5577463_+|alkaline-phosphatase	unknown	unknown	gnl|CDD|293736
NZ_CP042437.1|WP_147057630.1|5580084_5580903_+|phytanoyl-CoA-dioxygenase-family-protein	unknown	unknown	gnl|CDD|368580

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147057632.1|5580933_5582031_+|cellulase-family-glycosylhydrolase	gnl|CDD|367210	pfam02836, Glyco_hydro_2_C, Glycosyl hydrolases family 2, TIM barrel domain. This family contains beta-galactosidase, beta-mannosidase and beta-glucuronidase activities.	0.000180096
NZ_CP042437.1|WP_147057654.1|5600908_5601847_+|dihydrodipicolinate-synthase-family-protein	gnl|CDD|188630	cd00408, DHDPS-like, Dihydrodipicolinate synthase family. Dihydrodipicolinate synthase family. A member of the class I aldolases, which use an active-site lysine which stabilizes a reaction intermediate via Schiff base formation, and have TIM beta/alpha barrel fold. The dihydrodipicolinate synthase family comprises several pyruvate-dependent class I aldolases that use the same catalytic step to catalyze different reactions in different pathways and includes such proteins as N-acetylneuraminate lyase, MosA protein, 5-keto-4-deoxy-glucarate dehydratase, trans-o-hydroxybenzylidenepyruvate hydratase-aldolase, trans-2'-carboxybenzalpyruvate hydratase-aldolase, and 2-keto-3-deoxy- gluconate aldolase. The family is also referred to as the N-acetylneuraminate lyase (NAL) family.	1.45437e-92
NZ_CP042437.1|WP_147057652.1|5598405_5600640_+|glycoside-hydrolase-family-2	gnl|CDD|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	4.26078e-41
NZ_CP042437.1|WP_147057646.1|5594586_5595984_+|outer-membrane-beta-barrel-protein	gnl|CDD|369446	pfam07642, BBP2, Putative beta-barrel porin-2, OmpL-like. bbp2. BBP2 is a family of putative porin proteins that are likely to be outer membrane beta barrel proteins porins.	2.44811e-45
NZ_CP042437.1|WP_147057639.1|5588479_5589913_-|AAA-family-ATPase	gnl|CDD|376582	pfam01637, ATPase_2, ATPase domain predominantly from Archaea. This family contain a conserved P-loop motif that is involved in binding ATP. There are eukaryote members as well as archaeal members in this family.	5.89629e-09
NZ_CP042437.1|WP_147057624.1|5574059_5575571_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	gnl|CDD|369630	pfam07980, SusD_RagB, SusD family. This domain is found in bacterial cell surface proteins such SusD and SusD-like proteins, as as well RagB, outer membrane surface receptor antigen. Bacteroidetes, one of the two dominant bacterial phyla in the human gut, are Gram-negative saccharolytic microorganisms that utilize a diverse array of glycans. Hence, they express starch-utilization system (Sus) for glycan uptake. SusD has 551 amino acids, and is almost entirely alpha-helical, with 22 alpha-helices, eight of which form 4 tetra-trico peptide repeats (TPRs: helix-turn-helix motifs involved in protein-protein interactions). The four TPRs pack together to create a right-handed super-helix. This is predicted to mediate the formation of SusD and SusC porin complex at the cell surface. The interaction between SusC and TPR1/TPR2 region of SusD is predicted to be of functional importance since it allows SusD to be in position for oligosaccharide capture from other Sus lipoproteins and delivery of these glycans to the SusC porin. The non-TPR containing portion of SusD is where starch binding occurs. The binding site is a shallow surface cavity located on top of TPR1. SusD homologs such as SusD-like proteins have a critical role in carbohydrate acquisition. Both SusD and its homologs, contain about 15-20 residues at the N-terminus that might be a flexible linker region, anchoring the protein to the membrane and the glycan-binding domain. Other homologs to SusD have been examined in Porphyromonas gingivalis such as RagB, an immunodominant outer-membrane surface receptor antigen. Structural characterization of RagB shows substantial similarity with Bacteroides thetaiotaomicron SusD (i.e alpha-helices and TPR regions). Based on this structural similarity, functional studies suggest that, RagB binding of glycans occurs at pockets on the molecular surface that are distinct from those of SusD.	6.04749e-32
NZ_CP042437.1|WP_147057634.1|5582072_5582951_+|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.	1.38861e-35
NZ_CP042437.1|WP_147061068.1|5591479_5592652_+|M20/M25/M40-family-metallo-hydrolase	gnl|CDD|349902	cd05651, M20_ArgE_DapE-like, M20 peptidases with similarity to acetylornithine deacetylases and succinyl-diaminopimelate desuccinylases. Peptidase M20 family, uncharacterized protein subfamily with similarity to acetylornithine deacetylase/succinyl-diaminopimelate desuccinylase (ArgE/DapE) subfamily. ArgE/DapE enzymes catalyze analogous reactions and share a common activator, the metal ion (usually Co2+ or Zn2+). ArgE catalyzes a broad range of substrates, including N-acetylornithine, alpha-N-acetylmethionine and alpha-N-formylmethionine, while DapE catalyzes the hydrolysis of N-succinyl-L,L-diaminopimelate (L,L-SDAP) to L,L-diaminopimelate and succinate. Proteins in this subfamily are bacterial, and have been inferred by homology as being related to both ArgE and DapE.	0
NZ_CP042437.1|WP_147057650.1|5596905_5598252_+|deoxyguanosinetriphosphate-triphosphohydrolase	gnl|CDD|234897	PRK01096, PRK01096, deoxyguanosinetriphosphate triphosphohydrolase-like protein; Provisional.	7.06612e-161
NZ_CP042437.1|WP_147057630.1|5580084_5580903_+|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.	2.76685e-19
NZ_CP042437.1|WP_147061069.1|5590994_5591465_+|GNAT-family-N-acetyltransferase	gnl|CDD|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	0.000478414
NZ_CP042437.1|WP_147061067.1|5585573_5586557_+|type-IX-secretion-system-membrane-protein-PorP/SprF	gnl|CDD|274625	TIGR03519, bacteroidetes-specific_membrane_protein, type IX secretion system membrane protein, PorP/SprF family. This model describes a protein family unique to, and greatly expanded in, the Bacteriodetes. Species in this lineage include several, such as Cytophaga hutchinsonii and Flavobacterium johnsoniae, that have type IX secretion systems (T9SS) and exhibit a poorly understood rapid gliding phenotype. Several members of this protein family are found in operons with other genes whose loss leads to a loss a this motility.	2.68423e-74
NZ_CP042437.1|WP_147057636.1|5583042_5585574_+|T9SS-type-B-sorting-domain-containing-protein	gnl|CDD|372639	pfam13585, CHU_C, C-terminal domain of CHU protein family. The function of this C-terminal domain is not known; there are several conserved tryptophan and asparagine residues.	6.06394e-29
NZ_CP042437.1|WP_147057638.1|5586561_5588325_+|OmpA-family-protein	gnl|CDD|143586	cd07185, OmpA_C-like, Peptidoglycan binding domains similar to the C-terminal domain of outer-membrane protein OmpA. OmpA-like domains (named after the C-terminal domain of Escherichia coli OmpA protein) have been shown to non-covalently associate with peptidoglycan, a network of glycan chains composed of disaccharides, which are crosslinked via short peptide bridges. Well-studied members of this family include the Escherichia coli outer membrane protein OmpA, the Escherichia coli lipoprotein PAL, Neisseria meningitdis RmpM, which interact with the outer membrane, as well as the Escherichia coli motor protein MotB, and the Vibrio flagellar motor proteins PomB and MotY, which interact with the inner membrane.	3.8326e-33
NZ_CP042437.1|WP_147057656.1|5601921_5602923_+|4-hydroxyproline-epimerase	gnl|CDD|184428	PRK13971, PRK13971, 4-hydroxyproline epimerase.	0
NZ_CP042437.1|WP_147057644.1|5592626_5593967_+|response-regulator	gnl|CDD|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	7.02784e-157
NZ_CP042437.1|WP_147057626.1|5575627_5577463_+|alkaline-phosphatase	gnl|CDD|293736	cd16012, ALP, Alkaline Phosphatase. Alkaline phosphatases are non-specific membrane-bound phosphomonoesterases that catalyze the hydrolysis reaction via a phosphoseryl intermediate to produce inorganic phosphate and the corresponding alcohol, optimally at high pH. Alkaline phosphatase exists as a dimer, each monomer binding 2 zinc atoms and one magnesium atom, which are essential for enzymatic activity. Mammalian alkaline phosphatase is divided into four isozymes depending upon the site of tissue expression. They are Intestinal ALP, Placental ALP, Germ cell ALP and tissue nonspecific alkaline phosphatase or liver/bone/kidney (L/B/K) ALP.	1.78582e-108

Protein sequences

>NZ_CP042437.1|WP_147057639.1|5588479_5589913_-|AAA-family-ATPase
MKEIIGRVTEKQLLEQTLKADEAELIAMYGRRRVGKTYLIRKTFQKQLIFEFSGIHNAPLKEQLTNFRNTIAPLLKLSIPLPVPLNWTEAFLILKNYAEPLLKKNKCVIFLDEFPWLSSPKSGFLSAFEFFWNSWGTKQNNLIVTICGSAASWMIQKVVNNKGGLHNRITKKIRLLPFTLAETSDYLNNNNVNLDQYQITQLYMALGGIPQYLKEIAPGQSAAQNIDRICFTKDGALQGEFNNLYQSLFSEADKHVAIVKALAAKPAGLTRKEIIAACHLSTGGTTTLLLQELTESGFISAYLPFAKNTRDSIYKLSDEYSRFYLKFIENSRATGTGTWIKLSAAPSWGSWSGTAFESICLKHTREIKAALGIAGVYTEESAWRHVPGKKQPGAQIDLLFDRQDFCISICEIKFSNTVFTIDKAYAAELVQKCEVFKSNTKTSKTLFIVMVTTFGTQDNSYKTGLVQNDIVLQDLFR
>NZ_CP042437.1|WP_147057638.1|5586561_5588325_+|OmpA-family-protein
MKKLIMIVLLMALLAKVTLAQEQLSVKQRADKLFDQYEYFKSLKFYLKLVGHKPDVKVVERIATCYRYINQYQDAEDWYAKALNDPKAAKIDHYFYAEVLFRNQKFDQARQQYQLYFTDDAGALALKLADVDSAMVWMMQPSPYKVNNVGGVNTPSSDWGTAYGGQTTIIFTSDRENEDGKRDNRTGNGWFKLYTYDLNTKETKQLFLDPGTSKEFKDAYHVGPMVLNNKGDTAYITLTTEVAAKNLPIDQHSGKSSPRLYTRRLQLVTAVKKDGGWVISGSFPYNNVLQYSVGNAALSKDGSLIYFSSDMQGGQGKTDIWYCEKQSNGSWGKPVNCGKAINSKQEESFPFVDENGVLYYASKGLPGMGGYEIYAAHGQKNSWDTPKNLKYPINSTSDDFNLITRDGQSGYLSSNRDNGQGSDDIYAFTRVKDSIFVKPITGNPQLIVASGKPGSPGSPDPLSGASRPDFNIRPIYYDLDKSFIRPDAAVELDSLAGILKQYPALKIALASYCDSRASYLYNLALSQRRAKSAVTYLVKKGIAPTRMAAKGYSESNLVNQCADKVKCSEADHQLNRRTEIKVVSGSN
>NZ_CP042437.1|WP_147061067.1|5585573_5586557_+|type-IX-secretion-system-membrane-protein-PorP/SprF
MRGFKLYFLVAGLVLLTVKLQAQQSIQFSQYMFNGLAVNPAYAGYKQDWTLNLSSRIQWVGINDAPKTGTVSVDGLTNSTNQNMGLGLIATFDKLGPESTSSVYVNYAYRLRLDEDDTKRLSFGLGFGAIQYRLDGTKFNATDDGDANIPAGTQSNVTPDFRFGVYYYSPTVYVGASVFNLLSGLGNTVDHLQQYKQARTVYLTGGAMVPLNETMDIKPSLLIKEDFKGPTNLDVSNYIVFNKTIWVGASYRTGINLWKKSNLQSGLDKTDAVAAMVQFYISENFRIGYSYDFTTSRLASSQSGSHELSLSISFPGKSPRVVSPRYF
>NZ_CP042437.1|WP_147057636.1|5583042_5585574_+|T9SS-type-B-sorting-domain-containing-protein
MLNSAVIFCGMPYPYFKLIIKGFFCAVILFFLQVGGLYAEGSKELAANGGYRAYLFSSSTVANSSFPFPTLGTVKVYVKAGESIYVGSSAQGIAGGTINLRAPDGNNYTSGTDVNTGNINSRAQEVAGPLPNAGGFTPFIKTAGAGQEGVWEIDFVAENPGTVLNGNPPTIPANANWTQPQAEYITAFDVSVRNASNSGFINGRVYTQVFSGILGTFNVGFNAIFHILTKDGYQYILNNNGQAGNGFTFFVNNKGFRGADGNASYKSINGLSANVNVQDPRVADTQTDITQKIFFNIPATDMPAVANTPGSATTWLLNTPVVPAISNVTFTGAEGTVGKAGTNPLGGNFNFNITGNGNYVIGIDINHNGVYSDAIDRKLTGQATTGGNQVYWDGLDGLGAKVAGNSSLSLQVDITIATTAGEVHFPFFDVERNVNGLLLTRTNGTYAPDDTLYWDDTPISIVGTPSNPVKNLTGLSSAINGHKWGTTTSIATNDADFGNNKSIDTWSYIKSKPVTTSVSFVMQEADLSVESITAVAACSGQPVVYKVVVKNNGPNNVTGAGFSFSFPNDISGVVVTSAATTGSSSTSGGAVVANAYHANLDIANGAVRTFTITGNIALATSGNLTVEAAVLRPADVTDPDATNPDAAIPTDPNNECDASPSGVGCNNVKTNTVNIAPGPNAGADQTIFEYAPATMAATGTGVFTQVAGDPLPATISTPASNTTIITGLDKVGLYHFVFTNANGCADTVVLKVIAADLQIPNVITPNNDGKNDTFKIVGLESYPGSQLTVFNRWGNEVYRSDNYKNDWSGTGLAEATYFYVLNRKEHTGEFTPVKGWVFLKLSK
>NZ_CP042437.1|WP_147057634.1|5582072_5582951_+|helix-turn-helix-domain-containing-protein
MIKPTLETLSGHGNSTFLVRIFEETEFASPYHFHPEYELTAILKGEGNRFVGNNMSAYQKGDLVLLGGNVPHCWKTGLRTEDINARSVVIQFDRGFLGTAFFEDHHAWQVVQLLDKSLQGIQFTGAKAQAIIDLMLTMAKTDNEFKRLIMLLEVLDKLTEADDYKLLNEQPFIYRSTVTEHNRLNTIQAFIIDNFRNRVSLKQVADLAVMTPNAFCKFYKKMTGKTLIEVVTQYRLNYAMQLLIASNKTATEISFESGFADVAYFHKLFRQYTKHSPQVYRKEYLRKLRNVV
>NZ_CP042437.1|WP_147057632.1|5580933_5582031_+|cellulase-family-glycosylhydrolase
MKKIFLLLIMITGIGAAFAQNTGKRWTEERVWKWYNQQPWYCGFNYIPAYAINYTAMWDKTSFNAAAIDKELALAGQSGMNSLRAVLQYAVYADDPEYFLNTLDKFMAICEKHHIKFIPALFDDCSFGIDNDPKIGRQPEPLPGWYAWAWSPSPGHSLVVDSATHPKLEKYVKAVIGRFKNDPRILMWDLYNEPTNGGLGSATFPLLKKVIIWARAIDPVQPLTIGIFDQNPRLNSIITDNADLITFHDYGNKDNVIKTIEKLKQYNRPMINTEWMNRPWKSTVSEIIPVFYQYKVGCNLWGLVNGKTQTNLPWGHRPGDPEQKLWQHDLYHGDFKAYKTAEIDSLKMFIDKSKTIQYIQQHQHK
>NZ_CP042437.1|WP_147057630.1|5580084_5580903_+|phytanoyl-CoA-dioxygenase-family-protein
MISPKTPVLNSFIDVDERQISNFRLHGHVLLPNILQANEVAYYRNIIRQAAYRHNTETRAMQHRDTYGKAFLQVMNLWNTDEDVKQFTLAKRFAKIAADLLGVNHVRVYHDQALFKEPGGGFTPWHQDQYYWPLDTTNTVTMWMPLIDIDVELGMLTFASGSHLDGFAENIPISDESETALQKYVAQKKYPISRAERMRAGDATWHYGWTLHNAPGNSTASTTREVMTIIYYADGAHITAPQNKHQETDRNRWLGGLNPGQPANSHLNPLVY
>NZ_CP042437.1|WP_147057628.1|5578130_5579624_-|TonB-dependent-receptor
MNAIHNKDIGTKQKALAINLDPKIYGSFAEIGAGQDVAANFFKAGASSGTIAKTMSAYDMVFSDAIYGVQQSRRYVSEARLISMLDHEYGLLIERLAVQRGDSTTFFAFSDTVSALNYNKTNDGHGWMGVRFQLTPNSAFNDVVIHVKLLDNDTNLQQQAVGILGVNLMYACFYYNEIPPVFLLSLMDNLSRDRIQIDMIRFEGPDFTKVDNRLMSLHLVKYGFSDAAVFGPDGKNMQPTEALYKKHIVVIRGRFRPIINVHLDMLNNGVKQFLQEPDVDKSKVVVVTELTLQALKERNADLNADIDEKDFLDRVDILCSLGQTVMISNFHEYYKLVAYLSKITRLKIGMVLGFPNLEYIFSEEHYQDLPGGILESFATLFSRKVKLFIYPTLRDGVIWNCLKFYPPPHLIDLYRYLIANNKIEDIRHYTEGNLHVDTDKVLQLIKQGAAGWEEYVPNEVAAMIKDRCLFGFHCEVPPVNVVAAANESDTQTQTAAV
>NZ_CP042437.1|WP_147057626.1|5575627_5577463_+|alkaline-phosphatase
MVKIIRTATMLALLTGMSIAAHAQIKAYTVADAHSHNDYKNNIPFYRAYEKGFGSIEADVYAVNGQLMVAHDKKEISAKRSLKILYIDPLIEKFNRDPQRHLRLLIEIKEDYKAILPLVISELKPLEKYFAYDGHPGRLSIVMTGAVPPAAVMPNYPDWISFDVDHLDGFTAAQWKKIGLVSFPLSKYVHWNGKGVFNADEIKRIKGGIDSVHNAGKKVRFYETPDTKSSWLAMLRLGVDVIGTDDIEGLGNFLNRKEKSEYKAPEPYVIYHPSYKSDGTVKKVKNIILCIGDGMGLSQLYATYSANRGQLNIFQMLNMGFSVTYSADAYITDSAAGATAFASGQKTNDRAIGVDPAGKPLRSLADYSADAGKKTADIVVCELTDATPAAFYAHDSERSHSTNIANQIVSSPVDIFLGSAYKDFTQPVDGQTPIDKMKQRGYTIIRNFDDFLNTPATKILALMDDSVTRPKMDGRGNYLPLALKKVTQTFKSAPNGFFMMIEGSQIDHGGHTNNLKQVITENSDFDRMVGDALRFADEDGETLVIVTADHETGGLTLLDGNIAKGYVWGDFSTNDHTGTPVPIFAYGPHSLDFRGVFNNTEIFNKLKALIK
>NZ_CP042437.1|WP_147057624.1|5574059_5575571_+|RagB/SusD-family-nutrient-uptake-outer-membrane-protein
MKFKNIVKGLLGVMVIILAQSCNKSTLDNIKPTGTPTSTNFWKNASDAQAAANGLYEKQSNSEDLYGRGYFWLIDASDDMVVGRTSADRENIKNFVCTGNESSIYAPWSLHFVVMKRANDVIANVPGITMDQATKNFILGQAYFVHAVMHLEIADLYGTDKQGAPVQNRANPIAFPAQLASVKDNYAYIAADLKKAASLLPYFDQLAATDKGRAHKTAAWAYLAKTYLHAKDYANAEKYADSVISSGKHALLANYADVFKIANNYSSEYIWSVASNLNGQSILPGAMLENKGWGLYNGFGYFQPTKELVDEFETGDKRLAATILKSGDIFQYFGQTYTYPIGGKSNSLTGYQFNKYMEPFSYAGGIHISPNGDEPSTDLNVPLLRYAEILLIKAEAQIMQGKNGDVALNLVRVRAGLAPKSGATMADLKHERRVELAGEWSDRNFDLVRWGDAQATYAKPLHGANGSVVWKARNFDPARDNVWPIPPKDIQISQGQLKQNAGW
>NZ_CP042437.1|WP_147057642.1|5590524_5590707_+|hypothetical-protein
MTSFYIVLEVAAFIAVIVIPMAGPKAKKNVPVATTSNLAVNNEGYLEPIPANQQDHHPVH
>NZ_CP042437.1|WP_147061069.1|5590994_5591465_+|GNAT-family-N-acetyltransferase
MESSAIARGSGISKRSAASVIEKIDAGKAIVAITQNGEWAGFSYIETWDDEKFVSNSGLIVSPKHRNNGIASQIKTQIFELSRSKYPAAKIFSITSGLAIMKMNTKLGFVPVTYTEVTRETRFWDSCKSCVNYDVLQSKNRCNCLCTAMLFDPQLN
>NZ_CP042437.1|WP_147061068.1|5591479_5592652_+|M20/M25/M40-family-metallo-hydrolase
MIKDLNQRLSFAKAAKSLPLNPHFFSESVALLQHLIRTPSFSGEESDVADIVHQYLFGYSVKVKRKGNNLWCFNKFYDENKPTILLNSHLDTVMPNEGYTKDPFCPEIIDGKLYGLGSNDAGGCLVSLIATFLHFYSYQGLGFNLCLAVTAEEENSGENGIKSLLPQLGKLELAIVGEPTLLQMAVAEKGNLVIDCVSNGRSGHAARDEGDNAIHKCLKDLEWFSTYQFPQQLKSLPPVKMTVTTIKAGMQHNIVPARCEFTVDIRNDDTFSQRQILDTILKNVSCQVNVRPGALGASSIPVNHPIVKTGIAIGCKTYSSPTTSDQAWLSVPSIKIGPGDSARSHSSDEFIYLEEIKKGISLYIRLLDALPLMLINNPNKYKNEIKHINN
>NZ_CP042437.1|WP_147057644.1|5592626_5593967_+|response-regulator
MKSSILIIDDEVKLSELMARILTLEGYQVMQAANAKAGIKLVEREDIRVVLSDVKLPDANGVDLVERIKKIKPYIEIINLTAFGTISDGVLAIKNGAFDYLTKGDDNDKIIPLVSKAIDKANLQYQVSELQKQAEAQHGFPVVLGQSAAILEAVDLAKKVAHTDATVLLLGETGTGKEVFAEAIHAESLRKDKPFVAVNCSAFSKELLESELFGYKAGAFTGAVKDKKGLFEEASGGTIFLDELGEMSHDLQAKLLRVLENGTFIKIGEAKTTKVNVRLVAATNRDLQKESEEGHFRLDLFYRLSGFSIVLPPLRERVGDIEVLARHFIKLYSAKVKKKQPDVDPNFFKLLNQHKWNGNIRELKNVIERVIILMDEPVLTPKLLPNEFHNGGYYDLVALDLHSVEKHHIRRILKYVKGNKTEAARVLGIGLATLYRKIEEYQILLN
>NZ_CP042437.1|WP_147057646.1|5594586_5595984_+|outer-membrane-beta-barrel-protein
MKKLFLSIFVGSLFTTAYAQNPTAVVKKDSVAVTDSVKTKPEPFAFGDFTWLNGNDRRHKALLDTKYFTGRFLLDFNYTASNNNPIDHTVVGSTALARDHEFEISTVAFGGDFHYDNIRASVLTQFGTRSTVVPRNDFSVTRGQFDLSTAYRYLSEANAGYHFNVLNGINVDAGIFMSYIGLFSYYNAENWAYQPSFTSDNTPWFFNGVRVQIFVSDKLKIEPWLINGWQSYGMFNSRPGIGGQILWRPKEWLQILSNNYYGADTQDKPGRKRFHTDNSIEVRYFKSSNKGSFVNSAAFSVTGDLGDEKGDGVNGFTSDPVKGPAQYFASAMLYHRMVMAKGHLGWTVGGGFMNNPGRYLVLYPTGDANPIPAINTGAVGTHPFSANPGDKFKAYDYSTTVDLMPNDYLTFRLEVVHRHANVPYFAGHGGVTSPDGYNTTTLPADFKPDLVNSETRFIAALLVRF
>NZ_CP042437.1|WP_147057648.1|5596125_5596728_+|hypothetical-protein
MKNSIKMLIAFVVISLQISTLYAYDKTNNTGVYLTEQDYKAGKLSYILSNGDSMHLNDFLGGNHISIRYQGKKIKLSKKQVFGYRQDNQDFRFYQNQAYRVLDTAGFLLYTRDGLEQQGKGPKAVAKYFYSVNTQEPVLNLTLQNVIQSFPADSDFCYSVQNNFHQDADLMIFDRVNRQYEIKHLYLGHKHNLNNQHAAI
>NZ_CP042437.1|WP_147057650.1|5596905_5598252_+|deoxyguanosinetriphosphate-triphosphohydrolase
MMNWETLLSAKRWGYEDKYVASQVDARSEFQRDYDRIIFSSPFRRLQNKTQVFPLPGSIFVHNRLTHSLEVASVGKSLGRIFYNRLKEEDPGIDARLPLMSDIDTIISAACLAHDLGNPAFGHSGEAAISHYFIEGDGAGYRKNMPDEQWADLINFEGNANALRILTHAYSGKGNGSFALTYATIAAIAKYPCASIVGGNKANIHTKKYGFFQSEQAGFRKIADELGLNKVQDNPPIYKRHPLVYLVEAADDICYNIIDIEDAHRLKILSYDEIEALLLPLCNDPKMKARLDDIDDDDAKVGYLRARSINTLIQQCSKLFYNQQQNILAGDFNTSLIDMIDEPYRTIMKNIETLSVKKIYNYSSVVQIEVAGYKVMGGILEEFIPAYLQNSSKYHKKLVELIPRQFLTQNQDDYSKIQTVLDFVSGMTDLYAVELFRKIKGISFPTLS
>NZ_CP042437.1|WP_147057652.1|5598405_5600640_+|glycoside-hydrolase-family-2
MNLKKILCLAAMIMPSLLIAQQWQPKKAVLMTRFAKDVNPNCVLPEYPRPQFARVKWLNLNGVWQYQPGAAGDALPKGKLSKTILVPFPVESALSGVMEHHDRLWYRRKFTVPAAWKGQHVLLHFGAVDYESEVFVNGKSFGVHKGGYDPFSYDITSAITGAGPQEITVRVFDATDDAGEPRGKQSLHPQGIMYTPTTGIWQTVWLEPVPVTNINDIRITPDIDKSVVKLTVSTAAKAARYTVAIKVKDGVKVVQTYSGKAGQELSVPVKNAKLWSPDSPFLYNLDISLQKDGKSVDMVSSYFGMRKISVGDEDGYKKLFLNNKFLFQIGPLDQGFWPDGIYTAPTDAAIKNDLQMIKNYGFNMVRKHIKVEPYRWYYWADKLGLMVWQDMPSENSYTEHTPPIDSVAYASELTRMIKTHWNTPSIVTWVVFNEAQGQHNTAGLVNMVRKLDDSRLINQASGGNHFGVGDFMDIHSYPPPAVPESKTQVLACGEYGGIGYIIPGHIWKSGPTYIMIDNKKDYTNLYDTYANDLVLYKTNKGLSAAVYTEITDVEVELNGLLTYDREVDKGGVANISASNKKIINDHMYISDVLPSSQTNSRDWKYTFSKPEDGWFNTQYNDAAWKLGPGGFGTSFTPGVNVKTVWNSSDIWIRQDFTLNETRAINKDNLVLYIHHDETCEVYINGVKAATIDGGTSGYTVAPISKEGKAALNLKGKNTIAIHCHQTVGGQYIDAGISLLSKTKP
>NZ_CP042437.1|WP_147057654.1|5600908_5601847_+|dihydrodipicolinate-synthase-family-protein
MITFDWKGVFPAVTTKFTDNDELDFDAFDVNLAAQLEAGVDGFILGGSLGEASVLTDDEKFALLKHTIEYVDGKVPVILNIAEQTTKAAVACAKRAFDTGADGLMLLPPMRYNSEERETLAYIGAVAESTELPIMIYNNPVDYKIEVTLDMFEKLAVYKNIQAVKESTRNVSNVTKMFNRFGNRYAIFTGVDPLAMESLVMGADGWVAGLVDAFPKETVAIYRLVKAGRIAEALTIYRWFLPVLELDIHPKLVQYIKLAEVATGIGTENVRAPRLPLIGEERTKVLKIINDALAVRPELPVGSWGKLTEVEA
>NZ_CP042437.1|WP_147057656.1|5601921_5602923_+|4-hydroxyproline-epimerase
MSSKTFFCIDAHTCGNPVRVVAGGGPTLKGDNMSQKRQHFLKEYDWIRTGLMFEPRGHDMMSGSILFPPHDPANDVAVLFIETSGCLPMCGHGTIGTITIAIEEGLIQPKIPGIVRMEAPAGLVLIEYKQEGKKVTSVKLRNVAAYLAATNLEVECPDLGMLTIDVSYGGNYYAIVDPQPNFAGLENYTAGQLIAWSQVLRKRINEKYKFVHPQDPTINTCTHILWAGATLDSTSTARNAVFYGDKAIDRSPCGTGTSARMAQWYAKGKLKVGEPFIHESIIGSKFTGKVEDVVKIGELDAIIPSVEGWAKVYGYNTIKIDDDDPYAHGFQVI

Crispr_ID: NZ_CP042437_12

• CRISPR_ID: NZ_CP042437_12
• CRISPR_location: 6222636-6231258
• CRISPR_type: orTypeII
• Repeat_type: NA
• Spacer_info: 113 spacers
• Cas_protein_info: cas2,cas1,cas9

Consensus repeat of NZ_CP042437_12

Consensus_repeat	Method
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CRISPRCasFinder
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	PILER-CR
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	PILER-CR

spacers of NZ_CP042437_12

>12.1|6222682|30|NZ_CP042437|CRISPRCasFinder
ATCGGTTAATTGGGGCAGGGCCTTACTTAA
>12.2|6222758|29|NZ_CP042437|CRISPRCasFinder
TATGGTAACTGGTCATGAACTCGGCCGGT
>12.3|6222833|30|NZ_CP042437|CRISPRCasFinder
ATGGCAGTTTCACAAACGTGCCGGTTTCGA
>12.4|6222909|30|NZ_CP042437|CRISPRCasFinder
AACTGCTTATACCACCTTTATTCAAACCCT
>12.5|6222985|30|NZ_CP042437|CRISPRCasFinder
ACCACCCCTTTTTTTTAAAAAAAAGGGAAC
>12.6|6223061|30|NZ_CP042437|CRISPRCasFinder
GGTAACGCTAACATTTACAACAGAAAGCCT
>12.7|6223137|29|NZ_CP042437|CRISPRCasFinder
CGCAAACGCATCGCCATACGCCGATCTGA
>12.8|6223212|30|NZ_CP042437|CRISPRCasFinder
GGTTGGGATATAAGTCAAAACCCTTCAAAG
>12.9|6223288|30|NZ_CP042437|CRISPRCasFinder
GCTTACCCGCAGGCTGTATTTAGGGTTTGT
>12.10|6223364|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CGGCAAGGTGTTTAGAACCTTCCGCAGGCA
>12.11|6223440|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CCGTTCCGAGTTCGGAATGGTTTGAAATTA
>12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TGACGGCAAGCTGCTGCCCGGATGGGATAT
>12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTTTACTTTTGAAATAAGCATCTACATATT
>12.14|6223668|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CAAGTGGATAATAAGGATTGATAGCTATTT
>12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AGGGGTTTAAAATAAAAAAGCCTCACAAGT
>12.16|6223820|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTTGCTTTTTTATGATCAACCTCGCCGCCT
>12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TAAAGAAGATGATGTAAATTTTGCCGATCG
>12.18|6223972|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AAGTTGCAGCAATTATAAACCGGAAATCAC
>12.19|6224048|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GCTTACCCGCAGGCTGTATTTAGGGTTTGT
>12.20|6224124|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TGATCCCATTGCCGGCATGACCGCATTGCG
>12.21|6224200|29|NZ_CP042437|CRISPRCasFinder,PILER-CR
CCGGAAAATGGTGTACGCAAGAGAGCTCG
>12.22|6224275|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
ACTATTAATGAAGCGCAGTTATTACGATTA
>12.23|6224351|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CAAGTGGATAATAAGGATTGATAGCTATTT
>12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AGGGGTTTAAAATAAAAAAGCCTCACAAGT
>12.25|6224503|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CCAGGCTCGAAAGGTAGGGCGCTGCATAGA
>12.26|6224579|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GCTGTTTAAGATATGTAGGTATCCTGATAA
>12.27|6224655|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
ATATCCCAAAAGCAGGTAAAGCTTCCTTGC
>12.28|6224731|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CTATACAGCGAAAAGCGTGTATCTGACGGT
>12.29|6224807|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CCCAGTCTGTAGACGAATTGTCTACCGGAG
>12.30|6224883|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CACTAACGCTTCATCCGCTCTACGTTTAAC
>12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CCACGTAGATATATATAAAGATTTTTACCT
>12.32|6225035|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTAACAAACGAATAACCGCATCCGTACCAT
>12.33|6225111|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TGCATCAGGAAAATAAACAGCATGATTTGT
>12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TCTGAATCTGAAAATAAGATAAAAGAATTA
>12.35|6225263|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTCTTTTCGGTGTTTTTAATCGGTAATCTT
>12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TGTTTTTGTTACATAAATTGTATACCCTGC
>12.37|6225415|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTGTTTCCGATTATCACAAAGAACAAAAGC
>12.38|6225491|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GGAAATATTTGGTAATTGCTTTTAATAGTT
>12.39|6225567|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TGATTTAGTGAACAGGCCCGAACTTGCATT
>12.40|6225643|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AATCATCTTTATGCAGATTAGGTATGATTG
>12.41|6225719|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTTGATTTTTGTTTGAAGTTTTTCATATTC
>12.42|6225795|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AGGTTGGGCTTACTTGCTTTACCAGCTAAC
>12.43|6225871|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTAATGTATTCAATGCTACGGTATTGGCAA
>12.44|6225947|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TATGATATCGAAGTATTGAACGATAGTATA
>12.45|6226023|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TCGTCAGTTTCCGGCGCATCGTTTGTGGTC
>12.46|6226099|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GTGATGGTATCTTTTTACAACGTCTTCAGG
>12.47|6226175|29|NZ_CP042437|CRISPRCasFinder,PILER-CR
ACTAAATGACATTTCTATGACAATTCAAC
>12.48|6226250|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTTACCAGTATAATCCAGGTAGCAGGCCGC
>12.49|6226326|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
>12.50|6226402|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
>12.51|6226478|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTTTTTGCGTTTTCATAGCGATTGTATCTG
>12.52|6226554|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CACTATCGAAGAGTTTAGGGGTATTTACAA
>12.53|6226630|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GCTACGCATCAGGCGTGCCAAAGCCATATC
>12.54|6226706|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TACTGACCGGGATTACCCAATTTGGGATAA
>12.55|6226782|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GGTACCCAGTACGGCCACCAGGGCATTATT
>12.56|6226858|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AGCTCAGCGCGGTATTTAGCGATACGTCTG
>12.57|6226934|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AATTGCACATTGTTTATATGACGGTAAAAG
>12.58|6227010|29|NZ_CP042437|CRISPRCasFinder,PILER-CR
TACTAACTATATCGCCCCACACTTCGCTA
>12.59|6227085|29|NZ_CP042437|CRISPRCasFinder,PILER-CR
ATAGTAATGGGCGTAGTAAGTATAACGCC
>12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTGGCACAATGCTAAGATTGATGATATAAT
>12.61|6227236|29|NZ_CP042437|CRISPRCasFinder,PILER-CR
CACATCTTTACCCCGACTTTCGACGGCTG
>12.62|6227311|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CGCGGTTCAGATCGCGGCAAACATCTTCTA
>12.63|6227387|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
ATAGCCATGATATTTAATAGGGGTTTTAAA
>12.64|6227463|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AGTGCCTGCGTATGCCCAAATATCGGTGCC
>12.65|6227539|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CGCTGTTCAGTTCGTACGCAGCACCCCAAT
>12.66|6227615|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TGAGCCAGCCAAATGCGCCGCCTACGCCAC
>12.67|6227691|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CAATCGGTTAAACGTGGGAATGAACATGCA
>12.68|6227767|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GCGCCAATGATAATGGCAATGGCAAGGAGA
>12.69|6227843|30|NZ_CP042437|CRISPRCasFinder
CCAACCACCCGCCGGAACTCCAACAAGCGT
>12.70|6227919|30|NZ_CP042437|CRISPRCasFinder
CAATCGGTTAAACGTGGGAATGAACATGCA
>12.71|6227995|30|NZ_CP042437|CRISPRCasFinder
AAATGGTGGCTGATAAACAGCTACAAAACC
>12.72|6228071|30|NZ_CP042437|CRISPRCasFinder
CATTCTAAATTTGACAACTCAACAGCTAAA
>12.73|6228147|30|NZ_CP042437|CRISPRCasFinder
TGAGGAAAAATTAGGTTATGGTGCATCATT
>12.74|6228223|30|NZ_CP042437|CRISPRCasFinder
TCATCAACCGTACATAGCCATTCACTGTAA
>12.75|6228299|30|NZ_CP042437|CRISPRCasFinder
ACAAATTAATTCACATAAATCAAAAACAAT
>12.76|6228375|30|NZ_CP042437|CRISPRCasFinder
TTCATACCCAGGGACATCTACCATAAATGG
>12.77|6228451|30|NZ_CP042437|CRISPRCasFinder
CTGATGGTGTATTTAGCCTGGAAAAGCTTG
>12.78|6228527|30|NZ_CP042437|CRISPRCasFinder
ACTTTGGCTCGGGCTTCTTTCCAAATATCT
>12.79|6228603|30|NZ_CP042437|CRISPRCasFinder
GGCAGCGACTTTAGGGAACGCGAGGCTTTA
>12.80|6228679|30|NZ_CP042437|CRISPRCasFinder
ACATTTCTTTTTGGACTTTAACCATTACAG
>12.81|6228755|30|NZ_CP042437|CRISPRCasFinder
ACGGCCATCTATCCAAACAACAGTGTAATT
>12.82|6228831|30|NZ_CP042437|CRISPRCasFinder
CTAAATGGGGTTTTAATGTGCCTTTCGCAT
>12.83|6228907|30|NZ_CP042437|CRISPRCasFinder
TTTGTCATTGGTAGTTACCTGTTCAACCCT
>12.84|6228983|30|NZ_CP042437|CRISPRCasFinder
TAACCGCAATTTCGGGACTGCCGCGCTTGC
>12.85|6229059|30|NZ_CP042437|CRISPRCasFinder
GCGCGGCTAATGTTCCCATGCTTTCGGCGA
>12.86|6229135|30|NZ_CP042437|CRISPRCasFinder
CAATCGGTTAAACGTGGGAATGAATATGCA
>12.87|6229211|30|NZ_CP042437|CRISPRCasFinder
TAGGAGCATTCAAATCAACAGCAAACAGCA
>12.88|6229287|30|NZ_CP042437|CRISPRCasFinder
ACAATCGGTTAAACGTGGGAATGAATATGC
>12.89|6229363|30|NZ_CP042437|CRISPRCasFinder
ATACAACAGACAATTACAATACAATCGGTT
>12.90|6229439|30|NZ_CP042437|CRISPRCasFinder
AAAGGACGTTATCATATAACGCACCGACAC
>12.91|6229515|30|NZ_CP042437|CRISPRCasFinder
CGCAATCGGCTCTATCTTTCCCGGTATTGG
>12.92|6229591|30|NZ_CP042437|CRISPRCasFinder
TGAACCCGCAGCCCTTAACAGGTTTCCTAC
>12.93|6229667|30|NZ_CP042437|CRISPRCasFinder
CATGGCCGCTTCTTTTGCCCTACGGGCTAC
>12.94|6229743|30|NZ_CP042437|CRISPRCasFinder
CCATTTTTTCTATAACTACCTGGCCGGTAT
>12.95|6229819|30|NZ_CP042437|CRISPRCasFinder
CCTCTCAAAATCTCAAAACGACGCATTAGG
>12.96|6229895|30|NZ_CP042437|CRISPRCasFinder
AAGTAGCCAACCACCAGCAGGAACACCAAC
>12.97|6229971|29|NZ_CP042437|CRISPRCasFinder
ATTTAACTGGTGCCCGTTTAATTAAAGAG
>12.98|6230046|30|NZ_CP042437|CRISPRCasFinder
TTGTGGTAGTAGCGCCTATGATAGTACCTG
>12.99|6230122|30|NZ_CP042437|CRISPRCasFinder
AGTACCTCTATCGGAAGTCGAGAGCCGATA
>12.100|6230198|29|NZ_CP042437|CRISPRCasFinder
AACCAATAGCGGCGGAACGAACCCAACAA
>12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GTACCAATGCTAATGGCAATGGCCAGGCGG
>12.102|6230349|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
AACGAACCCAACAATAACGTTCACAAGCCC
>12.103|6230425|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TACAAAACACACCAGGAATAGACTGTAACG
>12.104|6230501|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TAACCGACTAAATGTTGGAATGAACATGCA
>12.105|6230577|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TAACAGACTAAACGTCGGCATGAATATGCA
>12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GTACCAATGCTAATGGCAATGGCCAGGCGG
>12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR
ATAAGCGGAGGAAGCTACGAAGACTGGGT
>12.108|6230804|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
CTTGCACATGGGTGTGCGGTATGGAAGTTT
>12.109|6230880|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TTGCTAAACGTCCGGCCGAATATAGGCAAC
>12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
GAGGCTAAAATACAAGTAAAGACAGCAAAA
>12.111|6231032|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TAAACATCCTTTTTTACGCAAGCTATCTAC
>12.112|6231108|30|NZ_CP042437|CRISPRCasFinder,PILER-CR
TGACTTAGTTAACAGGCCAGAACTTGCATT
>12.113|6231184|29|NZ_CP042437|CRISPRCasFinder,PILER-CR
AATAATATACAATCCTAAATCCAGGCTGT

CRISPR arrays and Neighbor proteins around NZ_CP042437_12

CRISPR arrays

The CRISPR arrays of NZ_CP042437_12

>merge|NZ_CP042437|12|6222636-6231258|CRISPRCasFinder,PILER-CR,PILER-CR
GTTGTGATTTGCTTTCAATCTTTAAACAACTGATATTTGGAACAACATCGGTTAATTGGGGCAGGGCCTTACTTAAGTTGTGATTTGCTTTCAATCTTTAAACAACTGATATTTGGAACAACTATGGTAACTGGTCATGAACTCGGCCGGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATGGCAGTTTCACAAACGTGCCGGTTTCGAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAACTGCTTATACCACCTTTATTCAAACCCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACCACCCCTTTTTTTTAAAAAAAAGGGAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGGTAACGCTAACATTTACAACAGAAAGCCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCGCAAACGCATCGCCATACGCCGATCTGAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGGTTGGGATATAAGTCAAAACCCTTCAAAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCTTACCCGCAGGCTGTATTTAGGGTTTGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCGGCAAGGTGTTTAGAACCTTCCGCAGGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCGTTCCGAGTTCGGAATGGTTTGAAATTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGACGGCAAGCTGCTGCCCGGATGGGATATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTTACTTTTGAAATAAGCATCTACATATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAAGTGGATAATAAGGATTGATAGCTATTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGGGGTTTAAAATAAAAAAGCCTCACAAGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTGCTTTTTTATGATCAACCTCGCCGCCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAAAGAAGATGATGTAAATTTTGCCGATCGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAGTTGCAGCAATTATAAACCGGAAATCACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCTTACCCGCAGGCTGTATTTAGGGTTTGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGATCCCATTGCCGGCATGACCGCATTGCGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCGGAAAATGGTGTACGCAAGAGAGCTCGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACTATTAATGAAGCGCAGTTATTACGATTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAAGTGGATAATAAGGATTGATAGCTATTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGGGGTTTAAAATAAAAAAGCCTCACAAGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCAGGCTCGAAAGGTAGGGCGCTGCATAGAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCTGTTTAAGATATGTAGGTATCCTGATAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATATCCCAAAAGCAGGTAAAGCTTCCTTGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTATACAGCGAAAAGCGTGTATCTGACGGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCCAGTCTGTAGACGAATTGTCTACCGGAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCACTAACGCTTCATCCGCTCTACGTTTAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCACGTAGATATATATAAAGATTTTTACCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTAACAAACGAATAACCGCATCCGTACCATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGCATCAGGAAAATAAACAGCATGATTTGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTCTGAATCTGAAAATAAGATAAAAGAATTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTCTTTTCGGTGTTTTTAATCGGTAATCTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGTTTTTGTTACATAAATTGTATACCCTGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTGTTTCCGATTATCACAAAGAACAAAAGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGGAAATATTTGGTAATTGCTTTTAATAGTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGATTTAGTGAACAGGCCCGAACTTGCATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAATCATCTTTATGCAGATTAGGTATGATTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTGATTTTTGTTTGAAGTTTTTCATATTCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGGTTGGGCTTACTTGCTTTACCAGCTAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTAATGTATTCAATGCTACGGTATTGGCAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTATGATATCGAAGTATTGAACGATAGTATAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTCGTCAGTTTCCGGCGCATCGTTTGTGGTCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGTGATGGTATCTTTTTACAACGTCTTCAGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACTAAATGACATTTCTATGACAATTCAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTACCAGTATAATCCAGGTAGCAGGCCGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCGGAAGTGCCGTTTTTGGGTTGAAGTCAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCGGAAGTGCCGTTTTTGGGTTGAAGTCAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTTTTGCGTTTTCATAGCGATTGTATCTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCACTATCGAAGAGTTTAGGGGTATTTACAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCTACGCATCAGGCGTGCCAAAGCCATATCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTACTGACCGGGATTACCCAATTTGGGATAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGGTACCCAGTACGGCCACCAGGGCATTATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGCTCAGCGCGGTATTTAGCGATACGTCTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAATTGCACATTGTTTATATGACGGTAAAAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTACTAACTATATCGCCCCACACTTCGCTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATAGTAATGGGCGTAGTAAGTATAACGCCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTGGCACAATGCTAAGATTGATGATATAATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCACATCTTTACCCCGACTTTCGACGGCTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCGCGGTTCAGATCGCGGCAAACATCTTCTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATAGCCATGATATTTAATAGGGGTTTTAAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGTGCCTGCGTATGCCCAAATATCGGTGCCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCGCTGTTCAGTTCGTACGCAGCACCCCAATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGAGCCAGCCAAATGCGCCGCCTACGCCACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAATCGGTTAAACGTGGGAATGAACATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCGCCAATGATAATGGCAATGGCAAGGAGAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCAACCACCCGCCGGAACTCCAACAAGCGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAATCGGTTAAACGTGGGAATGAACATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAATGGTGGCTGATAAACAGCTACAAAACCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCATTCTAAATTTGACAACTCAACAGCTAAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGAGGAAAAATTAGGTTATGGTGCATCATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTCATCAACCGTACATAGCCATTCACTGTAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACAAATTAATTCACATAAATCAAAAACAATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTCATACCCAGGGACATCTACCATAAATGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTGATGGTGTATTTAGCCTGGAAAAGCTTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACTTTGGCTCGGGCTTCTTTCCAAATATCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGGCAGCGACTTTAGGGAACGCGAGGCTTTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACATTTCTTTTTGGACTTTAACCATTACAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACGGCCATCTATCCAAACAACAGTGTAATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTAAATGGGGTTTTAATGTGCCTTTCGCATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTGTCATTGGTAGTTACCTGTTCAACCCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAACCGCAATTTCGGGACTGCCGCGCTTGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCGCGGCTAATGTTCCCATGCTTTCGGCGAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAATCGGTTAAACGTGGGAATGAATATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAGGAGCATTCAAATCAACAGCAAACAGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACAATCGGTTAAACGTGGGAATGAATATGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATACAACAGACAATTACAATACAATCGGTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAAGGACGTTATCATATAACGCACCGACACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCGCAATCGGCTCTATCTTTCCCGGTATTGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGAACCCGCAGCCCTTAACAGGTTTCCTACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCATGGCCGCTTCTTTTGCCCTACGGGCTACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCATTTTTTCTATAACTACCTGGCCGGTATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCTCTCAAAATCTCAAAACGACGCATTAGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAGTAGCCAACCACCAGCAGGAACACCAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATTTAACTGGTGCCCGTTTAATTAAAGAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTGTGGTAGTAGCGCCTATGATAGTACCTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGTACCTCTATCGGAAGTCGAGAGCCGATAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAACCAATAGCGGCGGAACGAACCCAACAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGTACCAATGCTAATGGCAATGGCCAGGCGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAACGAACCCAACAATAACGTTCACAAGCCCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTACAAAACACACCAGGAATAGACTGTAACGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAACCGACTAAATGTTGGAATGAACATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAACAGACTAAACGTCGGCATGAATATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGTACCAATGCTAATGGCAATGGCCAGGCGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATAAGCGGAGGAAGCTACGAAGACTGGGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTTGCACATGGGTGTGCGGTATGGAAGTTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTGCTAAACGTCCGGCCGAATATAGGCAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGAGGCTAAAATACAAGTAAAGACAGCAAAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAAACATCCTTTTTTACGCAAGCTATCTACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGACTTAGTTAACAGGCCAGAACTTGCATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAATAATATACAATCCTAAATCCAGGCTGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC

>NZ_CP042437|12|12|6222636-6231258|CRISPRCasFinder
GTTGTGATTTGCTTTCAATCTTTAAACAACTGATATTTGGAACAAC	ATCGGTTAATTGGGGCAGGGCCTTACTTAA
GTTGTGATTTGCTTTCAATCTTTAAACAACTGATATTTGGAACAAC	TATGGTAACTGGTCATGAACTCGGCCGGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATGGCAGTTTCACAAACGTGCCGGTTTCGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AACTGCTTATACCACCTTTATTCAAACCCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACCACCCCTTTTTTTTAAAAAAAAGGGAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGTAACGCTAACATTTACAACAGAAAGCCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCAAACGCATCGCCATACGCCGATCTGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGTTGGGATATAAGTCAAAACCCTTCAAAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTTACCCGCAGGCTGTATTTAGGGTTTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGGCAAGGTGTTTAGAACCTTCCGCAGGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGTTCCGAGTTCGGAATGGTTTGAAATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGACGGCAAGCTGCTGCCCGGATGGGATAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTTACTTTTGAAATAAGCATCTACATATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAAGTGGATAATAAGGATTGATAGCTATTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGGGTTTAAAATAAAAAAGCCTCACAAGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTGCTTTTTTATGATCAACCTCGCCGCCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAAAGAAGATGATGTAAATTTTGCCGATCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AAGTTGCAGCAATTATAAACCGGAAATCAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTTACCCGCAGGCTGTATTTAGGGTTTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGATCCCATTGCCGGCATGACCGCATTGCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAAATGGTGTACGCAAGAGAGCTCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACTATTAATGAAGCGCAGTTATTACGATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAAGTGGATAATAAGGATTGATAGCTATTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGGGTTTAAAATAAAAAAGCCTCACAAGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCAGGCTCGAAAGGTAGGGCGCTGCATAGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTGTTTAAGATATGTAGGTATCCTGATAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATATCCCAAAAGCAGGTAAAGCTTCCTTGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTATACAGCGAAAAGCGTGTATCTGACGGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCCAGTCTGTAGACGAATTGTCTACCGGAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACTAACGCTTCATCCGCTCTACGTTTAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCACGTAGATATATATAAAGATTTTTACCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTAACAAACGAATAACCGCATCCGTACCAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGCATCAGGAAAATAAACAGCATGATTTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TCTGAATCTGAAAATAAGATAAAAGAATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTCTTTTCGGTGTTTTTAATCGGTAATCTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGTTTTTGTTACATAAATTGTATACCCTGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGTTTCCGATTATCACAAAGAACAAAAGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGAAATATTTGGTAATTGCTTTTAATAGTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGATTTAGTGAACAGGCCCGAACTTGCATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATCATCTTTATGCAGATTAGGTATGATTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTGATTTTTGTTTGAAGTTTTTCATATTC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGTTGGGCTTACTTGCTTTACCAGCTAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTAATGTATTCAATGCTACGGTATTGGCAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TATGATATCGAAGTATTGAACGATAGTATA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TCGTCAGTTTCCGGCGCATCGTTTGTGGTC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTGATGGTATCTTTTTACAACGTCTTCAGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACTAAATGACATTTCTATGACAATTCAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTACCAGTATAATCCAGGTAGCAGGCCGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTTTTGCGTTTTCATAGCGATTGTATCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACTATCGAAGAGTTTAGGGGTATTTACAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTACGCATCAGGCGTGCCAAAGCCATATC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACTGACCGGGATTACCCAATTTGGGATAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGTACCCAGTACGGCCACCAGGGCATTATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGCTCAGCGCGGTATTTAGCGATACGTCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATTGCACATTGTTTATATGACGGTAAAAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACTAACTATATCGCCCCACACTTCGCTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAGTAATGGGCGTAGTAAGTATAACGCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGGCACAATGCTAAGATTGATGATATAAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACATCTTTACCCCGACTTTCGACGGCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCGGTTCAGATCGCGGCAAACATCTTCTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAGCCATGATATTTAATAGGGGTTTTAAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGTGCCTGCGTATGCCCAAATATCGGTGCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCTGTTCAGTTCGTACGCAGCACCCCAAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGAGCCAGCCAAATGCGCCGCCTACGCCAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAATCGGTTAAACGTGGGAATGAACATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCGCCAATGATAATGGCAATGGCAAGGAGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCAACCACCCGCCGGAACTCCAACAAGCGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAATCGGTTAAACGTGGGAATGAACATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AAATGGTGGCTGATAAACAGCTACAAAACC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CATTCTAAATTTGACAACTCAACAGCTAAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGAGGAAAAATTAGGTTATGGTGCATCATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TCATCAACCGTACATAGCCATTCACTGTAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACAAATTAATTCACATAAATCAAAAACAAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTCATACCCAGGGACATCTACCATAAATGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTGATGGTGTATTTAGCCTGGAAAAGCTTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACTTTGGCTCGGGCTTCTTTCCAAATATCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGCAGCGACTTTAGGGAACGCGAGGCTTTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACATTTCTTTTTGGACTTTAACCATTACAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACGGCCATCTATCCAAACAACAGTGTAATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTAAATGGGGTTTTAATGTGCCTTTCGCAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTGTCATTGGTAGTTACCTGTTCAACCCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAACCGCAATTTCGGGACTGCCGCGCTTGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCGCGGCTAATGTTCCCATGCTTTCGGCGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAATCGGTTAAACGTGGGAATGAATATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAGGAGCATTCAAATCAACAGCAAACAGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACAATCGGTTAAACGTGGGAATGAATATGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATACAACAGACAATTACAATACAATCGGTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AAAGGACGTTATCATATAACGCACCGACAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCAATCGGCTCTATCTTTCCCGGTATTGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGAACCCGCAGCCCTTAACAGGTTTCCTAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CATGGCCGCTTCTTTTGCCCTACGGGCTAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCATTTTTTCTATAACTACCTGGCCGGTAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCTCTCAAAATCTCAAAACGACGCATTAGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AAGTAGCCAACCACCAGCAGGAACACCAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATTTAACTGGTGCCCGTTTAATTAAAGAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGTGGTAGTAGCGCCTATGATAGTACCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGTACCTCTATCGGAAGTCGAGAGCCGATA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AACCAATAGCGGCGGAACGAACCCAACAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTACCAATGCTAATGGCAATGGCCAGGCGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AACGAACCCAACAATAACGTTCACAAGCCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACAAAACACACCAGGAATAGACTGTAACG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAACCGACTAAATGTTGGAATGAACATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAACAGACTAAACGTCGGCATGAATATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTACCAATGCTAATGGCAATGGCCAGGCGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAAGCGGAGGAAGCTACGAAGACTGGGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTTGCACATGGGTGTGCGGTATGGAAGTTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGCTAAACGTCCGGCCGAATATAGGCAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GAGGCTAAAATACAAGTAAAGACAGCAAAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAAACATCCTTTTTTACGCAAGCTATCTAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGACTTAGTTAACAGGCCAGAACTTGCATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATAATATACAATCCTAAATCCAGGCTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC

>NZ_CP042437|12|1|6223318-6227842|PILER-CR
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGGCAAGGTGTTTAGAACCTTCCGCAGGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGTTCCGAGTTCGGAATGGTTTGAAATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGACGGCAAGCTGCTGCCCGGATGGGATAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTTACTTTTGAAATAAGCATCTACATATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAAGTGGATAATAAGGATTGATAGCTATTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGGGTTTAAAATAAAAAAGCCTCACAAGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTGCTTTTTTATGATCAACCTCGCCGCCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAAAGAAGATGATGTAAATTTTGCCGATCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AAGTTGCAGCAATTATAAACCGGAAATCAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTTACCCGCAGGCTGTATTTAGGGTTTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGATCCCATTGCCGGCATGACCGCATTGCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAAATGGTGTACGCAAGAGAGCTCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACTATTAATGAAGCGCAGTTATTACGATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAAGTGGATAATAAGGATTGATAGCTATTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGGGTTTAAAATAAAAAAGCCTCACAAGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCAGGCTCGAAAGGTAGGGCGCTGCATAGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTGTTTAAGATATGTAGGTATCCTGATAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATATCCCAAAAGCAGGTAAAGCTTCCTTGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTATACAGCGAAAAGCGTGTATCTGACGGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCCAGTCTGTAGACGAATTGTCTACCGGAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACTAACGCTTCATCCGCTCTACGTTTAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCACGTAGATATATATAAAGATTTTTACCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTAACAAACGAATAACCGCATCCGTACCAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGCATCAGGAAAATAAACAGCATGATTTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TCTGAATCTGAAAATAAGATAAAAGAATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTCTTTTCGGTGTTTTTAATCGGTAATCTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGTTTTTGTTACATAAATTGTATACCCTGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGTTTCCGATTATCACAAAGAACAAAAGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGAAATATTTGGTAATTGCTTTTAATAGTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGATTTAGTGAACAGGCCCGAACTTGCATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATCATCTTTATGCAGATTAGGTATGATTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTGATTTTTGTTTGAAGTTTTTCATATTC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGTTGGGCTTACTTGCTTTACCAGCTAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTAATGTATTCAATGCTACGGTATTGGCAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TATGATATCGAAGTATTGAACGATAGTATA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TCGTCAGTTTCCGGCGCATCGTTTGTGGTC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTGATGGTATCTTTTTACAACGTCTTCAGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACTAAATGACATTTCTATGACAATTCAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTACCAGTATAATCCAGGTAGCAGGCCGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTTTTGCGTTTTCATAGCGATTGTATCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACTATCGAAGAGTTTAGGGGTATTTACAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTACGCATCAGGCGTGCCAAAGCCATATC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACTGACCGGGATTACCCAATTTGGGATAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGTACCCAGTACGGCCACCAGGGCATTATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGCTCAGCGCGGTATTTAGCGATACGTCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATTGCACATTGTTTATATGACGGTAAAAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACTAACTATATCGCCCCACACTTCGCTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAGTAATGGGCGTAGTAAGTATAACGCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGGCACAATGCTAAGATTGATGATATAAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACATCTTTACCCCGACTTTCGACGGCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCGGTTCAGATCGCGGCAAACATCTTCTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAGCCATGATATTTAATAGGGGTTTTAAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGTGCCTGCGTATGCCCAAATATCGGTGCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCTGTTCAGTTCGTACGCAGCACCCCAAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGAGCCAGCCAAATGCGCCGCCTACGCCAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAATCGGTTAAACGTGGGAATGAACATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCGCCAATGATAATGGCAATGGCAAGGAGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCAACCACCCGCCGGAACTCCAACAAGCGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAATCGGTTAAACGTGGGAATGAACATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAATGGTGGCTGATAAACAGCTACAAAACCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCATTCTAAATTTGACAACTCAACAGCTAAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGAGGAAAAATTAGGTTATGGTGCATCATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTCATCAACCGTACATAGCCATTCACTGTAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACAAATTAATTCACATAAATCAAAAACAATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTCATACCCAGGGACATCTACCATAAATGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTGATGGTGTATTTAGCCTGGAAAAGCTTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACTTTGGCTCGGGCTTCTTTCCAAATATCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGGCAGCGACTTTAGGGAACGCGAGGCTTTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACATTTCTTTTTGGACTTTAACCATTACAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACGGCCATCTATCCAAACAACAGTGTAATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTAAATGGGGTTTTAATGTGCCTTTCGCATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTGTCATTGGTAGTTACCTGTTCAACCCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAACCGCAATTTCGGGACTGCCGCGCTTGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCGCGGCTAATGTTCCCATGCTTTCGGCGAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAATCGGTTAAACGTGGGAATGAATATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAGGAGCATTCAAATCAACAGCAAACAGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACAATCGGTTAAACGTGGGAATGAATATGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATACAACAGACAATTACAATACAATCGGTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAAGGACGTTATCATATAACGCACCGACACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCGCAATCGGCTCTATCTTTCCCGGTATTGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGAACCCGCAGCCCTTAACAGGTTTCCTACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCATGGCCGCTTCTTTTGCCCTACGGGCTACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCATTTTTTCTATAACTACCTGGCCGGTATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCTCTCAAAATCTCAAAACGACGCATTAGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAGTAGCCAACCACCAGCAGGAACACCAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATTTAACTGGTGCCCGTTTAATTAAAGAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTGTGGTAGTAGCGCCTATGATAGTACCTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGTACCTCTATCGGAAGTCGAGAGCCGATAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAACCAATAGCGGCGGAACGAACCCAACAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTACCAATGCTAATGGCAATGGCCAGGCGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AACGAACCCAACAATAACGTTCACAAGCCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACAAAACACACCAGGAATAGACTGTAACG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAACCGACTAAATGTTGGAATGAACATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAACAGACTAAACGTCGGCATGAATATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTACCAATGCTAATGGCAATGGCCAGGCGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAAGCGGAGGAAGCTACGAAGACTGGGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTTGCACATGGGTGTGCGGTATGGAAGTTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGCTAAACGTCCGGCCGAATATAGGCAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GAGGCTAAAATACAAGTAAAGACAGCAAAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAAACATCCTTTTTTACGCAAGCTATCTAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGACTTAGTTAACAGGCCAGAACTTGCATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATAATATACAATCCTAAATCCAGGCTGT


>NZ_CP042437|12|2|6230227-6231258|PILER-CR
	CGGCAAGGTGTTTAGAACCTTCCGCAGGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGTTCCGAGTTCGGAATGGTTTGAAATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGACGGCAAGCTGCTGCCCGGATGGGATAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTTACTTTTGAAATAAGCATCTACATATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAAGTGGATAATAAGGATTGATAGCTATTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGGGTTTAAAATAAAAAAGCCTCACAAGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTGCTTTTTTATGATCAACCTCGCCGCCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAAAGAAGATGATGTAAATTTTGCCGATCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AAGTTGCAGCAATTATAAACCGGAAATCAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTTACCCGCAGGCTGTATTTAGGGTTTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGATCCCATTGCCGGCATGACCGCATTGCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAAATGGTGTACGCAAGAGAGCTCG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACTATTAATGAAGCGCAGTTATTACGATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAAGTGGATAATAAGGATTGATAGCTATTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGGGTTTAAAATAAAAAAGCCTCACAAGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCAGGCTCGAAAGGTAGGGCGCTGCATAGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTGTTTAAGATATGTAGGTATCCTGATAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATATCCCAAAAGCAGGTAAAGCTTCCTTGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTATACAGCGAAAAGCGTGTATCTGACGGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCCAGTCTGTAGACGAATTGTCTACCGGAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACTAACGCTTCATCCGCTCTACGTTTAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCACGTAGATATATATAAAGATTTTTACCT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTAACAAACGAATAACCGCATCCGTACCAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGCATCAGGAAAATAAACAGCATGATTTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TCTGAATCTGAAAATAAGATAAAAGAATTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTCTTTTCGGTGTTTTTAATCGGTAATCTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGTTTTTGTTACATAAATTGTATACCCTGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGTTTCCGATTATCACAAAGAACAAAAGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGAAATATTTGGTAATTGCTTTTAATAGTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGATTTAGTGAACAGGCCCGAACTTGCATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATCATCTTTATGCAGATTAGGTATGATTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTGATTTTTGTTTGAAGTTTTTCATATTC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGGTTGGGCTTACTTGCTTTACCAGCTAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTAATGTATTCAATGCTACGGTATTGGCAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TATGATATCGAAGTATTGAACGATAGTATA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TCGTCAGTTTCCGGCGCATCGTTTGTGGTC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTGATGGTATCTTTTTACAACGTCTTCAGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ACTAAATGACATTTCTATGACAATTCAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTACCAGTATAATCCAGGTAGCAGGCCGC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CCGGAAGTGCCGTTTTTGGGTTGAAGTCAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTTTTTGCGTTTTCATAGCGATTGTATCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACTATCGAAGAGTTTAGGGGTATTTACAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCTACGCATCAGGCGTGCCAAAGCCATATC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACTGACCGGGATTACCCAATTTGGGATAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GGTACCCAGTACGGCCACCAGGGCATTATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGCTCAGCGCGGTATTTAGCGATACGTCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATTGCACATTGTTTATATGACGGTAAAAG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACTAACTATATCGCCCCACACTTCGCTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAGTAATGGGCGTAGTAAGTATAACGCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGGCACAATGCTAAGATTGATGATATAAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CACATCTTTACCCCGACTTTCGACGGCTG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCGGTTCAGATCGCGGCAAACATCTTCTA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAGCCATGATATTTAATAGGGGTTTTAAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AGTGCCTGCGTATGCCCAAATATCGGTGCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CGCTGTTCAGTTCGTACGCAGCACCCCAAT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGAGCCAGCCAAATGCGCCGCCTACGCCAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CAATCGGTTAAACGTGGGAATGAACATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GCGCCAATGATAATGGCAATGGCAAGGAGA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCAACCACCCGCCGGAACTCCAACAAGCGTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAATCGGTTAAACGTGGGAATGAACATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAATGGTGGCTGATAAACAGCTACAAAACCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCATTCTAAATTTGACAACTCAACAGCTAAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGAGGAAAAATTAGGTTATGGTGCATCATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTCATCAACCGTACATAGCCATTCACTGTAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACAAATTAATTCACATAAATCAAAAACAATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTCATACCCAGGGACATCTACCATAAATGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTGATGGTGTATTTAGCCTGGAAAAGCTTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACTTTGGCTCGGGCTTCTTTCCAAATATCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGGCAGCGACTTTAGGGAACGCGAGGCTTTAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACATTTCTTTTTGGACTTTAACCATTACAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACGGCCATCTATCCAAACAACAGTGTAATTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCTAAATGGGGTTTTAATGTGCCTTTCGCATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTTGTCATTGGTAGTTACCTGTTCAACCCTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAACCGCAATTTCGGGACTGCCGCGCTTGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACGCGCGGCTAATGTTCCCATGCTTTCGGCGAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCAATCGGTTAAACGTGGGAATGAATATGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTAGGAGCATTCAAATCAACAGCAAACAGCAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACACAATCGGTTAAACGTGGGAATGAATATGCGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATACAACAGACAATTACAATACAATCGGTTGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAAGGACGTTATCATATAACGCACCGACACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCGCAATCGGCTCTATCTTTCCCGGTATTGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTGAACCCGCAGCCCTTAACAGGTTTCCTACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCATGGCCGCTTCTTTTGCCCTACGGGCTACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCATTTTTTCTATAACTACCTGGCCGGTATGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACCCTCTCAAAATCTCAAAACGACGCATTAGGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAAGTAGCCAACCACCAGCAGGAACACCAACGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACATTTAACTGGTGCCCGTTTAATTAAAGAGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACTTGTGGTAGTAGCGCCTATGATAGTACCTGGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAGTACCTCTATCGGAAGTCGAGAGCCGATAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAACAACCAATAGCGGCGGAACGAACCCAACAAGTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTACCAATGCTAATGGCAATGGCCAGGCGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AACGAACCCAACAATAACGTTCACAAGCCC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TACAAAACACACCAGGAATAGACTGTAACG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAACCGACTAAATGTTGGAATGAACATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAACAGACTAAACGTCGGCATGAATATGCA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GTACCAATGCTAATGGCAATGGCCAGGCGG
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	ATAAGCGGAGGAAGCTACGAAGACTGGGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	CTTGCACATGGGTGTGCGGTATGGAAGTTT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TTGCTAAACGTCCGGCCGAATATAGGCAAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	GAGGCTAAAATACAAGTAAAGACAGCAAAA
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TAAACATCCTTTTTTACGCAAGCTATCTAC
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	TGACTTAGTTAACAGGCCAGAACTTGCATT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC	AATAATATACAATCCTAAATCCAGGCTGT
GTTGTGATTTGCTTTCATTCTTTGAACAACTGATATTTGAATCAAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147058649.1|6242876_6243329_+|pyridoxamine-5'-phosphate-oxidase-family-protein	unknown	unknown	gnl|CDD|225998
NZ_CP042437.1|WP_147061092.1|6221585_6222431_-|alpha/beta-fold-hydrolase	unknown	unknown	gnl|CDD|223669
NZ_CP042437.1|WP_147058647.1|6242326_6242875_+|hypothetical-protein	unknown	unknown	gnl|CDD|372273
NZ_CP042437.1|WP_147058654.1|6245097_6246219_-|alpha-1,6-mannanase	unknown	unknown	gnl|CDD|367601
NZ_CP042437.1|WP_147058638.1|6231458_6231788_-|CRISPR-associated-endonuclease-Cas2	cas2	COG3512_cas2_CAS-II-A:CAS-II-B:CAS-II-C	gnl|CDD|226043
NZ_CP042437.1|WP_147058636.1|6220944_6221514_-|dihydrofolate-reductase	unknown	unknown	gnl|CDD|223340
NZ_CP042437.1|WP_147058651.1|6243753_6244539_-|exodeoxyribonuclease-III	unknown	unknown	gnl|CDD|197320
NZ_CP042437.1|WP_147058628.1|6217817_6218801_+|aldo/keto-reductase	unknown	unknown	gnl|CDD|381304
NZ_CP042437.1|WP_147058640.1|6231791_6232832_-|type-II-CRISPR-associated-endonuclease-Cas1	cas1	cd09720_cas1_CAS-II-A:CAS-II-B:CAS-II-C	gnl|CDD|274694
NZ_CP042437.1|WP_147058634.1|6219967_6220795_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|180766
NZ_CP042437.1|WP_158642989.1|6244630_6244807_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147058626.1|6217416_6217812_+|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|380361
NZ_CP042437.1|WP_147058642.1|6232970_6235604_-|DEAD/DEAH-box-helicase-family-protein	unknown	unknown	gnl|CDD|223989
NZ_CP042437.1|WP_147058622.1|6214724_6215198_-|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein	unknown	unknown	gnl|CDD|224991
NZ_CP042437.1|WP_147058632.1|6219308_6219821_+|DUF4440-domain-containing-protein	unknown	unknown	gnl|CDD|379639
NZ_CP042437.1|WP_147058643.1|6235605_6237192_-|site-specific-DNA-methyltransferase	unknown	unknown	gnl|CDD|225100
NZ_CP042437.1|WP_147058645.1|6237949_6241684_+|type-II-CRISPR-RNA-guided-endonuclease-Cas9	cas9	cd09643_cas9_CAS-II-A:CAS-II-B:CAS-II-C	gnl|CDD|273840
NZ_CP042437.1|WP_147058624.1|6215510_6216407_-|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl|CDD|197666
NZ_CP042437.1|WP_147058620.1|6214086_6214728_-|cytochrome-c	unknown	unknown	unknown
NZ_CP042437.1|WP_147058630.1|6218811_6219270_+|cupin-domain-containing-protein	unknown	unknown	gnl|CDD|380361

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP042437.1|WP_147058638.1|6231458_6231788_-|CRISPR-associated-endonuclease-Cas2	cas2	COG3512_cas2_CAS-II-A:CAS-II-B:CAS-II-C	2.1e-32	106.5	0.1
NZ_CP042437.1|WP_147058645.1|6237949_6241684_+|type-II-CRISPR-RNA-guided-endonuclease-Cas9	cas9	cd09643_cas9_CAS-II-A:CAS-II-B:CAS-II-C	5.3e-66	218.3	31.7
NZ_CP042437.1|WP_147058640.1|6231791_6232832_-|type-II-CRISPR-associated-endonuclease-Cas1	cas1	cd09720_cas1_CAS-II-A:CAS-II-B:CAS-II-C	2.8e-82	270.7	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147058649.1|6242876_6243329_+|pyridoxamine-5'-phosphate-oxidase-family-protein	gnl|CDD|225998	COG3467, COG3467, Predicted flavin-nucleotide-binding protein [General function prediction only].	4.3408e-27
NZ_CP042437.1|WP_147061092.1|6221585_6222431_-|alpha/beta-fold-hydrolase	gnl|CDD|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	1.57301e-25
NZ_CP042437.1|WP_147058647.1|6242326_6242875_+|hypothetical-protein	gnl|CDD|372273	pfam12724, Flavodoxin_5, Flavodoxin domain. This is a family of flavodoxins. Flavodoxins are electron transfer proteins that carry a molecule of non-covalently bound FMN.	1.47303e-16
NZ_CP042437.1|WP_147058638.1|6231458_6231788_-|CRISPR-associated-endonuclease-Cas2	gnl|CDD|226043	COG3512, COG3512, CRISPR-associated protein, Cas2 homolog [Defense mechanisms].	7.74786e-29
NZ_CP042437.1|WP_147058636.1|6220944_6221514_-|dihydrofolate-reductase	gnl|CDD|223340	COG0262, FolA, Dihydrofolate reductase [Coenzyme metabolism].	9.14649e-15
NZ_CP042437.1|WP_147058651.1|6243753_6244539_-|exodeoxyribonuclease-III	gnl|CDD|197320	cd09086, ExoIII-like_AP-endo, Escherichia coli exonuclease III (ExoIII) and Neisseria meningitides NExo-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Escherichia coli ExoIII, Neisseria meningitides NExo,and related proteins. These are ExoIII family AP endonucleases and they belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER, the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiencies. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity. For example, Neisseria meningitides Nape and NExo, and exonuclease III (ExoIII) and endonuclease IV (EndoIV) in Escherichia coli. NExo and ExoIII are found in this subfamily. NExo is the non-dominant AP endonuclease. It exhibits strong 3'-5' exonuclease and 3'-deoxyribose phosphodiesterase activities. Escherichia coli ExoIII is an active AP endonuclease, and in addition, it exhibits double strand (ds)-specific 3'-5' exonuclease, exonucleolytic RNase H, 3'-phosphomonoesterase and 3'-phosphodiesterase activities, all catalyzed by a single active site. Class II AP endonucleases have been classified into two families, designated ExoIII and EndoIV, based on their homology to the Escherichia coli enzymes ExoIII and endonuclease IV (EndoIV). This subfamily belongs to the ExoIII family; the EndoIV family belongs to a different superfamily.	7.80549e-137
NZ_CP042437.1|WP_147058628.1|6217817_6218801_+|aldo/keto-reductase	gnl|CDD|381304	cd19078, AKR_AKR13C1_2, AKR13C family of aldo-keto reductase (AKR). The AKR13C family includes Helicobacter pyroli aldehyde reductase (AKR13C1) and Thermotoga maritima aldo-keto reductase (AKR13C2). Aldehyde reductase (EC 1.1.1.21), also called aldose reductase, is a cytosolic NADPH-dependent oxidoreductase that catalyzes the reduction of a variety of aldehydes and carbonyls, including monosaccharides.	0
NZ_CP042437.1|WP_147058640.1|6231791_6232832_-|type-II-CRISPR-associated-endonuclease-Cas1	gnl|CDD|274694	TIGR03639, cas1_NMENI, CRISPR-associated endonuclease Cas1, subtype II/NMENI. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is a 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 variant of the NMENI subtype of CRISPR/Cas system.	5.82821e-105
NZ_CP042437.1|WP_147058634.1|6219967_6220795_+|SDR-family-oxidoreductase	gnl|CDD|180766	PRK06940, PRK06940, short chain dehydrogenase; Provisional.	6.33551e-156
NZ_CP042437.1|WP_147058626.1|6217416_6217812_+|cupin-domain-containing-protein	gnl|CDD|380361	cd02233, cupin_HNL-like, Granulicella tundricola hydroxynitrile lyase (GtHNL) and related proteins, cupin domain. This family includes archaeal, eukaryotic, and bacterial proteins homologous to hydroxynitrile lyase from Granulicella tundricola (GtHNL), a novel class of HNLs that does not show any sequence or structural similarity to any other HNL and does not contain conserved motifs typical of HNLs. HNLs comprise a diverse group of enzymes that vary in terms of their substrate specificity, enantioselectivity and the need for a co-factor. In plants, they catalyze the reversible cleavage of cyanohydrins, yielding HCN and aldehydes or ketones. Also included in this family is TM1010 from Thermotoga maritima, a protein of unknown function. Some but not all members of this family have N- or C-terminal carboxymuconolactone decarboxylase domains in addition to the cupin domain. Members of this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold capable of homodimerization.	9.67778e-58
NZ_CP042437.1|WP_147058654.1|6245097_6246219_-|alpha-1,6-mannanase	gnl|CDD|367601	pfam03663, Glyco_hydro_76, Glycosyl hydrolase family 76. Family of alpha-1,6-mannanases.	7.41235e-33
NZ_CP042437.1|WP_147058622.1|6214724_6215198_-|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein	gnl|CDD|224991	COG2080, CoxS, Aerobic-type carbon monoxide dehydrogenase, small subunit CoxS/CutS homologs [Energy production and conversion].	4.62228e-77
NZ_CP042437.1|WP_147058632.1|6219308_6219821_+|DUF4440-domain-containing-protein	gnl|CDD|379639	pfam14534, DUF4440, Domain of unknown function (DUF4440).	6.63564e-15
NZ_CP042437.1|WP_147058643.1|6235605_6237192_-|site-specific-DNA-methyltransferase	gnl|CDD|225100	COG2189, COG2189, Adenine specific DNA methylase Mod [DNA replication, recombination, and repair].	1.32341e-44
NZ_CP042437.1|WP_147058645.1|6237949_6241684_+|type-II-CRISPR-RNA-guided-endonuclease-Cas9	gnl|CDD|273840	TIGR01865, conserved_hypothetical_protein, CRISPR subtype II/NMENI RNA-guided endonuclease Cas9/Csn1. CRISPR loci appear to be mobile elements with a wide host range. This model represents a protein found only in CRISPR-containing species, near other CRISPR-associated proteins (cas), as part of the NMENI subtype of CRISPR/Cas locus. The species range so far for this protein is animal pathogens and commensals only.	1.46316e-59
NZ_CP042437.1|WP_147058624.1|6215510_6216407_-|helix-turn-helix-domain-containing-protein	gnl|CDD|197666	smart00342, HTH_ARAC, helix_turn_helix, arabinose operon control protein.	2.12103e-20
NZ_CP042437.1|WP_147058642.1|6232970_6235604_-|DEAD/DEAH-box-helicase-family-protein	gnl|CDD|223989	COG1061, SSL2, DNA or RNA helicases of superfamily II [Transcription / DNA replication, recombination, and repair].	1.0388e-07
NZ_CP042437.1|WP_147058630.1|6218811_6219270_+|cupin-domain-containing-protein	gnl|CDD|380361	cd02233, cupin_HNL-like, Granulicella tundricola hydroxynitrile lyase (GtHNL) and related proteins, cupin domain. This family includes archaeal, eukaryotic, and bacterial proteins homologous to hydroxynitrile lyase from Granulicella tundricola (GtHNL), a novel class of HNLs that does not show any sequence or structural similarity to any other HNL and does not contain conserved motifs typical of HNLs. HNLs comprise a diverse group of enzymes that vary in terms of their substrate specificity, enantioselectivity and the need for a co-factor. In plants, they catalyze the reversible cleavage of cyanohydrins, yielding HCN and aldehydes or ketones. Also included in this family is TM1010 from Thermotoga maritima, a protein of unknown function. Some but not all members of this family have N- or C-terminal carboxymuconolactone decarboxylase domains in addition to the cupin domain. Members of this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold capable of homodimerization.	1.21557e-50

Protein sequences

>NZ_CP042437.1|WP_147061092.1|6221585_6222431_-|alpha/beta-fold-hydrolase
MKPAFIIALLFFTVLQCYGQQLKPANSGYAPVNGIKVYYEVYGEGKPLVLLHGAFYTIEMNWGQLIPELAKTRKVIAVEMQGHGHTPFSDRKLDIATMASDVVGVMDFLKIDSADVAGYSMGGSIAYQLVVKSPKRVKKLVIISSTYKSGGWLPVINDGFKGFKPEFFNNTPIKTAYDAVAPDKTKWTKFIEQMIAFAGVPFDVGDANIAKITSPVLLISGDNDGLDKVELMKTYKLLGGGVAADLGPMPKSHLAIVPAQSHVSLMMQTKTIAGYLDDFLK
>NZ_CP042437.1|WP_147058636.1|6220944_6221514_-|dihydrofolate-reductase
MRKIRIFEHISLDGVIEHDGDYTYGAWTTPYRSPAGAAMLFEAYGPNFDLLLGRHTYDIFSSFWPNAGDFPMANAINAATKYIATHNPASLEWGPVQHLGEDVIEAIRDLKQTDGPDLIVVGSSTLTSVLLDQGLADEVVLITYPVLLGHGKRLLADSINARELVFVDSKATPTGLLVNTYRHVGPLKS
>NZ_CP042437.1|WP_147058634.1|6219967_6220795_+|SDR-family-oxidoreductase
MKNVIVVIGAGSIGQAIARRVSAGKHILLADLKQDNADAAAKVLGEAGFEVSTTTVDISSRTSVRALVEKATSIGSVTGLIQAAGVSPSQASPSTILHIDLYGNAVILEEFGKVIASGGSGVVIASQSGHRLPALTPEQDKALATTPADELLALDFLQPAQVKDSLRAYQLSKRGNSLRVMAEAVNWGKRGARINAISPGIIITPLAKDELNGPRGEGYRKMINISAAGRAGTPDEVGNVGALLMGQDGAFITGSDFLMDGGVTAAYWYGDLAPK
>NZ_CP042437.1|WP_147058632.1|6219308_6219821_+|DUF4440-domain-containing-protein
MKAIIIALFMCIAGVQLSLGQAKLPGAASTTTTKDEQELLDLSKTKWTWMAGKNVDALTGLFAENCVFVHMGGSWGKTQELNTIKGGFIWYKQAEVYGASVNIFGNTAILLNDIDLLAVVGGNEVVHAFMVTEVYLKENGKWKMGSLTFSTLIRPVKMKTNIAQPAQPQH
>NZ_CP042437.1|WP_147058630.1|6218811_6219270_+|cupin-domain-containing-protein
MKKLLLITCGLFAGFTMRATAQNAPVFPKGEISTVNNHTGTVWLTELNKADSTIDINVANATFAAGAKLDWHIHPAGQILMITEGTGYYQEKGKPIRIVHKGDVINCDPGVAHWHGASPNSLFTYIAVSTNSAKNKTIWLQRVTDAEYNSAN
>NZ_CP042437.1|WP_147058628.1|6217817_6218801_+|aldo/keto-reductase
MKKRQLGNSGLEVSALGLGCMGLSFGYGPATEKQEAIKLIHAAFERGVTFFDTAEAYGPFTNEELLGEALEPFRDQVVIATKFGFKDGKPPLGLDSRPEHIRKVAEAALIRLRTDHIDLFYQHRVDPNVPMEDVAGTVKDLIAEGKVKHFGLSEAGVGAIRKAHAIQPVAALQSEYSLWWREPEQDIIPVLEELGIGFVPFSPLGKGFLTGAINGSTTFDKSDFRNTVPRFSEENRKANQALVEVLGLIAKDKNATPAQIALAWLLSQKPWIVPIPGTTKMHRLEENLGAEDIRLSAKDLLEIGNSLSQIEVHGHRYSEQGQKMVNR
>NZ_CP042437.1|WP_147058626.1|6217416_6217812_+|cupin-domain-containing-protein
MKIQRIGSKPSAKGPAEYFTGTVRIDPLNEPPAPARVAMALVTFEPGARTAWHTHPFGQTLIVTAGAGWVQREGGVKENIFPGDVVYFEPNEKHWHGATTTTAMSHIAVQEKENGSPVDWLEQVTDEDYNG
>NZ_CP042437.1|WP_147058624.1|6215510_6216407_-|helix-turn-helix-domain-containing-protein
MDSMRRFNTISEYNAFNNNETRHPLVSVVDLSKAAPRQGSQMYFGFYIVFLKDVKCGDLVYGRNTYDYQEGTLVFMAPGQVAGVNSNGEYYQPKGHVLAFDADLIHGTSLGRHIQDYNFFSYQSNEALHLSEKERSIVLDCFSKINYELERGIDKHSKRLIVSNIELFLDYSVRFYDRQFITRDHVYKGTIEKFEKLLNNYFSSEKPQTVGLPSVAYCADELNLSPNYFGDLVKKETGKTAQEYIQFKLINLAKEKIFDGEKTVNQVAYELGFKYPQHFTRLFKKQVGQTPHEYRSLN
>NZ_CP042437.1|WP_147058622.1|6214724_6215198_-|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein
MININVNGTPHQIEADPNMPLLWVIRDIIGLTGTKFGCGVAQCGACVVHLNDQAVRSCVTKVSRAEGQKIVTIEGLSKNNDHPAQLAWNQEQVPQCGYCHSGQIMSAAVLLRENNNPSDADIDAAMAGNICRCGTYQRIRKAIRTAAELQRKESASK
>NZ_CP042437.1|WP_147058620.1|6214086_6214728_-|cytochrome-c
MKKQLKNKRRYTGVARAFAVVGVLLSAIAIMSFGLNSEPGKREAAPIVVRKDSVASVKAFKQVYSVLMSARCMNCHPSGNIPLQGDDSHLHTMSPQRGVDGKGVYAMKCANCHQATNTPGLHTPPGNPNWHLPPADMKMIFQGRSPRQLAKQIIDPKQNGHKDMKKLIEHADDGLVLSGWNPGEGRTLPPMSHAAFKKAWITWLTTGAYAPKK
>NZ_CP042437.1|WP_147058638.1|6231458_6231788_-|CRISPR-associated-endonuclease-Cas2
MRLNEYRILWVLVFFDLPTETKKDRQIYSKFRKDIMKDGFGMFQFSIYLRHCSSRENADVHIKRVKKILPPKGHVGIMTITDKQFGMMELFYGKEEKELPDTPQQLELF
>NZ_CP042437.1|WP_147058640.1|6231791_6232832_-|type-II-CRISPR-associated-endonuclease-Cas1
MIKRTLHFSNPAYLSLSQGQLMIDLPHLKVLGEKESKKSVPIEDVGIVVLEHQQITITHGCIAALLNNNSAIITCDHTHHPTGMMLPIDGHHTQSERFRYQVDASLPLKKQLWQQTTQAKILNQAAILAGRGIDHDNMLHWAKSVRSGDPDNYEGRAAAYYWKNVFPKKVEFFRGREGDPPNNLLNYGYAILRAIVARGLVCSGLIPTLGIHHRNKYNAYCLADDIMEPYRPYVDLIVLRIIDNGENFLELGNSIKSQLLAIATVDVQFEKSRSPLMVGVQNTTTSLARCYEGKLRKITYPMMKDFAPRRGVLYKDLEEDFISLAAEEEGKYYKAGDDDDEEELPF
>NZ_CP042437.1|WP_147058642.1|6232970_6235604_-|DEAD/DEAH-box-helicase-family-protein
MELKSYQYKVIRDLETYLEYVQQYKKTDRAFNLFWEERIGPYNPLSGEGMQPYKNTIPNAAHVCIKVPTAGGKTFIACNALHTVFSAYSAVMPRVVVWLVPWSNLLGQTVSALSNPAHPYRQKLNSLFNHRVEVYEKKDLLQGLNFNPAVVKEQLSIVVMSFASLRAKNKEDRKVYQENGQLASFASQYTNIGYLLQDVDETSLINVLRSMQPVIVVDESHNAESNLSVDMLNALNPSFVLDLTATPKNNSNIISMVPAIELKKEHMVKLPVIVYNHHDKTEVVNSALHLQRKLELLAIEQQKQGGRYIRPIVLFQAQPRIGEENITYEKLKRQLITIGIPQNQIRIKTATIDELRGEDLLSPLCEVRYIITINALKEGWDCPFAYVLASLADKSSAVDVEQILGRVLRQPYVTKHSASLLNISYVLTASAKFNDTLQNIVQGLQAAGFSDKDYREIDVMTETEKQAAIPGVLEQFLFPEKTGTDDPELDTNRINFDLGDTITPVANDSVLAKIEDMAIAQSAALQATINQQRTQPADEQIFEEMGDKIKRYKLVAAGKPYVAGIKLPQFYLNTGRANIFGTGREFLSQEPLLSLFKLSNEDIKIDFEQISSDLYKVDIEETGQSEYDARFTKIEDMVLKEPVVAYILAKPPSNQVKDIAHQLIKMIGDMYPIADQEIRIYIERILSSLNAEQLQDILVRKLSYADKIKAKIKQHADNYAEERFNDLIKIGKIEAEATWAFPEMIVPGMLGGAVSKSLYEREGLMNDFETTMIRNIAALPNITFWHRNLGRGKGFMINGYKSNHYPDFIVGTKLGKVILIETKGDDRDNSDSQAKCRLGNKWAELAGNRFSYFMVFDKKAIDGAYNADKARELIKQL
>NZ_CP042437.1|WP_147058643.1|6235605_6237192_-|site-specific-DNA-methyltransferase
MPTLTWIGKEKVITHHHDVPFKVLAHQYTFNTSAPPDLGEPSNKIIHGDNLEALKSLLPEYEGRVKCIYIDPPYNTGNESWVYNDNVNHPKLKKWLGQVVGKDSEDLTRHDKWLCMMYPRLVLLHKLLAKDGVIFISIDDNEQAVLKLICDEIFGGGNFVNNIIWQRAYAPVNTKKRFSPNHDFIICYGKDINALTFLLKRTDEANERYINPDNDKRGLYKPGDLSVGPIVEKQIYPITTPSGRIVYPPKGYCWRYTESRFQDLIADNRIWFGPDGNNVPAIKRFISEVKDGITPMTVWTYKEVGHTQDAKKDIKTIFSENELLFETPKAIKLMERIIQLATSSNSIILDSFAGSGTTAHAVLNLNKKDGGNRKFILIEMEDYAESITAERVKRVMQGYGGKEGTGGSFDYYILGEPLFVGENREYLNEAVGIDKIKNYVWYSETRTALDKFTPGAADDTLLGVHHNTAYYFIYHPERLTSLDFDSLVGINVQAGQYIVYADNCLLSKDFLFRHNIVFKKIPRDLSRF
>NZ_CP042437.1|WP_147058645.1|6237949_6241684_+|type-II-CRISPR-RNA-guided-endonuclease-Cas9
MKKILGLDIGTNSVGWALVHEPELPDESYSIAGIGVRIIPLSSDENDEFTKGNAMSKNADRTLRRGARRNLQRYKLRRRQLGILLEALNMMPDKKLFLLSALDLYGLRAKGVTEQLALQEIGRIFFHLNQKRGYKSNRKANNDEEQTAVTAAEETEASNAKPKKKGYLDLINDREQALKDEGITIGQHFYTQLLIDDKIRIKENIYLRSTYLDEFDRIWNKQQAYYPEVLTEDNKQKIRNETIYYQRPLRSQKGLVSNCLFEKHHKATPKSSPLFQVAKIWQELNNIELTSFKAMKGQEQGFDKQGKRPLTIEEKQSLFNLLTVKGKLTTKDCLKELGYKSGYDEYKLNIRNEKELEGNRTYAAIRKVFDHFKINHEELLQFNLTSDQKVNKQTGEVYGQLQIGAGFEREPLFQLWHLLYSVEEIDTLIAKLQSRYGFSPEAAKALAKIDFAKQGYGNLSAKAFRNIVPYLQKGLNYAEACKTAGYNHSNSQTTAQNEARDLIDKLELYPKNSLRQPVVEKIINQVINLVNEIIDENNGYVTNQERYKGAFEIRVELARELRQNAEERNKAYSRNSKQDKRHKEIEAIIKQLLPFRRVSRNDIERYKLWEEFGKVSPYEPQKAISLGELFSGEYDIEHIIPKSRLFDDSFSNKTICPKRLNSGSFGSKNQMTAHDFMKSQGDHTYNAYLEFIKIHLYKKDGISKAKFNKLMMSLDKIPEDFINRQLQETRFITKEVRNLLTQICRNVHATSGPVTSEIRHLWGWDDVIMDLQIDRYKTVNQTELIEYVTNGQTHKKEKIIGWSKREDHRHHAIDALTVACTKQGFINRINKVNAQENRDEMFNEVKGTRFNDRLSLLQKYLILQRPFETAKVLTAIDNILVSFKSGKKVTSNSNNLIKQGSSTHKTIEVIPRGFLHKETVYGRIKRFKEISLSPRFNNLKEVARREIRAQITEYLRQFDNDIKQAFNNKNLSLFKERTGYDKVVIYYYEHVVRYKLDTNFKVADVESIVDEGVKAIVKAHLAKYGNNPKEAFKNENTIWLNQEKGIAARSVRCFTGYTDLQPLHKNEYGEPIDFVITRNNHHIAIYRDKDGKMQENTVSFWDAVKRKQAKLPVIIKEPGMVWDEVINSGFDDQELLQGLPQPDWVYLTSLQQNEMFVFGLADKELQSAISVKNYALISKHLYRVQKMSKRSSGAIDLWFRHHLETKLDDSLAAKELNKFLNIQSLGGVNGMKVKVDNIGRIVKV
>NZ_CP042437.1|WP_147058647.1|6242326_6242875_+|hypothetical-protein
MNGIIVYQGKYGATEQYAQWLADELHMPFLKADEATPTILAGYDLVILGSSVYVGKLTIGKWLKRNSSILANKKIFLFIVCGTTAGDKAEQRLLLRTNLEPGVLKTTGVFFLPGRCVVSKLSWIDRFVLKLGAMLQKDPQKKAVMNHGFDHMNKKNLRSLVSAVGQECEVEAVMGSKATRRH
>NZ_CP042437.1|WP_147058649.1|6242876_6243329_+|pyridoxamine-5'-phosphate-oxidase-family-protein
MLGKLNEMQMEELLKKQVTGRIACTDAGVPYIVPVNYVYDGKQVIGHSTMGKKIEMMRKNPRVCFAVDDIKTIFNWQSVIAWGRFEEITDIAEKEQAMMAITHRLMPFAEKPANHPSHGLSEREDDIGTKLDLILYKIVLVNKTGRFERN
>NZ_CP042437.1|WP_147058651.1|6243753_6244539_-|exodeoxyribonuclease-III
MKIATYNVNGVNGRLPVLLRWLAETAPDVVCLQELKAPQDKFPLEAITGAGYNAIWHGQKSWNGVAILARSNYEIKELRKGLPGDPDDEHSRYIEAFINGIVIGCLYLPNGNPAPGPKLDYKLRWFERLTSHASGLLAHGIPTIITGDYNVMPTELDVYKPERWLDDALFRPEVRLAFKNLVDQGWTDAIRKLYPTEVIYTFFDYFRNAYGRNAGLRIDHFLLSPHVADRLQSAGVDRNVRGWEKTSDHCPVWIEIEESIK
>NZ_CP042437.1|WP_158642989.1|6244630_6244807_-|hypothetical-protein
MIIVKTDSFSTPARLALYINENNIKRENILTITDGARGLTIFFYGDSEVEEITHGLFS
>NZ_CP042437.1|WP_147058654.1|6245097_6246219_-|alpha-1,6-mannanase
MKKLTCFLALSIFTGFVSCSKGKDSAPAKTAVVKPVDQDFTAGDADLAYNAFNSAFYDSANKLYYSTTKKDGVAAIWTQAIYWDMAMNVYQRTKASSQLTMIGDIYQGNYNHYDGYNWSNQTVWFIYDDMMWWVMALARANQITGNATCLQKAKEGFDHVWAGSYDSVDGGMFWDFKHSGKNSCINFPTVIAAMRLYTITGDAGYLAKAKSIYTWSKTNLVDASGKVNDNKIGNNPAGGQDYTYNSGTAIGAALALYKQSNDAAYLDDARLYTDYVKNNLCTNGILPAEGDFNEQGVLKAIFAQYVMQLITEAGQTQYLSWIQTNVNTGWQNRDATRNLTYRNYAVACPTGDIQSYEASSIVTFMQLCPPTIK

Crispr_ID: NZ_CP042437_13

• CRISPR_ID: NZ_CP042437_13
• CRISPR_location: 6453747-6453834
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP042437_13

Consensus_repeat	Method
GGTGGTATTATGGCAGTTTAGTTTATT	CRISPRCasFinder

spacers of NZ_CP042437_13

>13.1|6453774|34|NZ_CP042437|CRISPRCasFinder
GGTTCACTTGTTCATTAGTTCATCGGTCTTTGCG

CRISPR arrays and Neighbor proteins around NZ_CP042437_13

CRISPR arrays

The CRISPR arrays of NZ_CP042437_13

>merge|NZ_CP042437|13|6453747-6453834|CRISPRCasFinder
GGTGGTATTATGGCAGTTTAGTTTATTGGTTCACTTGTTCATTAGTTCATCGGTCTTTGCGGGTGGTATTATGGCAGGTTAGTTTATT

>NZ_CP042437|13|13|6453747-6453834|CRISPRCasFinder
GGTGGTATTATGGCAGTTTAGTTTATT	GGTTCACTTGTTCATTAGTTCATCGGTCTTTGCG
GGTGGTATTATGGCAGGTTAGTTTATT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147058930.1|6440537_6441773_-|TolC-family-protein	unknown	unknown	gnl|CDD|224455
NZ_CP042437.1|WP_147058952.1|6454417_6456610_+|acylase	unknown	unknown	gnl|CDD|376618
NZ_CP042437.1|WP_147058946.1|6448909_6451288_+|TonB-dependent-receptor-plug-domain-containing-protein	unknown	unknown	gnl|CDD|274948
NZ_CP042437.1|WP_158642994.1|6444966_6447438_+|TonB-dependent-receptor	unknown	unknown	gnl|CDD|379720
NZ_CP042437.1|WP_147058966.1|6463730_6465131_-|GHKL-domain-containing-protein	unknown	unknown	gnl|CDD|223715
NZ_CP042437.1|WP_147058932.1|6442103_6443351_-|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl|CDD|223715
NZ_CP042437.1|WP_147058960.1|6460266_6461184_+|IS4-family-transposase	unknown	unknown	gnl|CDD|372999
NZ_CP042437.1|WP_147061096.1|6458571_6459207_+|DUF4291-family-protein	unknown	unknown	gnl|CDD|379483
NZ_CP042437.1|WP_147061097.1|6461060_6461477_+|transposase	unknown	unknown	gnl|CDD|376573
NZ_CP042437.1|WP_147058962.1|6461587_6461863_-|UBP-type-zinc-finger-domain-containing-protein	unknown	unknown	gnl|CDD|366940
NZ_CP042437.1|WP_147058934.1|6443347_6444025_-|response-regulator	unknown	unknown	gnl|CDD|223816
NZ_CP042437.1|WP_147058944.1|6448495_6448699_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147058958.1|6459636_6460068_+|DoxX-family-membrane-protein	unknown	unknown	gnl|CDD|311556
NZ_CP042437.1|WP_147058948.1|6451537_6452053_+|DUF2911-domain-containing-protein	unknown	unknown	gnl|CDD|378565
NZ_CP042437.1|WP_147058956.1|6457521_6458505_+|TIM-barrel-protein	unknown	unknown	gnl|CDD|366542
NZ_CP042437.1|WP_147058941.1|6447576_6448206_-|DUF47-family-protein	unknown	unknown	gnl|CDD|224310
NZ_CP042437.1|WP_147058936.1|6444293_6444707_+|EamA-family-transporter	unknown	unknown	gnl|CDD|225308
NZ_CP042437.1|WP_147058954.1|6456651_6457140_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147058950.1|6452631_6453714_+|DUF3810-family-protein	unknown	unknown	gnl|CDD|378933
NZ_CP042437.1|WP_147058964.1|6461872_6463534_-|FAD-dependent-oxidoreductase	unknown	unknown	gnl|CDD|381126

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147058930.1|6440537_6441773_-|TolC-family-protein	gnl|CDD|224455	COG1538, TolC, Outer membrane protein [Cell envelope biogenesis, outer membrane / Intracellular trafficking and secretion].	2.84968e-07
NZ_CP042437.1|WP_147058946.1|6448909_6451288_+|TonB-dependent-receptor-plug-domain-containing-protein	gnl|CDD|274948	TIGR04056, OMP_RagA_SusC, TonB-linked outer membrane protein, SusC/RagA family. This model describes a distinctive clade among the TonB-linked outer membrane proteins (OMP). Members of this family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 alone. Published descriptions of members of this family are available for RagA from Porphyromonas gingivalis, SusC from Bacteroides thetaiotaomicron, and OmpW from Bacteroides caccae. Members form pairs with members of the SusD/RagB family (pfam07980). Transporter complexes including these outer membrane proteins are likely to import large degradation products of proteins (e.g. RagA) or carbohydrates (e.g. SusC) as nutrients, rather than siderophores. [Transport and binding proteins, Unknown substrate].	4.9622e-14
NZ_CP042437.1|WP_158642994.1|6444966_6447438_+|TonB-dependent-receptor	gnl|CDD|379720	pfam14905, OMP_b-brl_3, Outer membrane protein beta-barrel family. This family includes proteins annotated as TonB dependent receptors. But it is also likely to contain other membrane beta barrel proteins of other functions.	4.21268e-82
NZ_CP042437.1|WP_147058966.1|6463730_6465131_-|GHKL-domain-containing-protein	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.00594e-33
NZ_CP042437.1|WP_147058932.1|6442103_6443351_-|HAMP-domain-containing-histidine-kinase	gnl|CDD|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.04143e-25
NZ_CP042437.1|WP_147058960.1|6460266_6461184_+|IS4-family-transposase	gnl|CDD|372999	pfam14294, DUF4372, Domain of unknown function (DUF4372). This domain family is found in bacteria, and is approximately 80 amino acids in length. The family is found in association with pfam01609. There is a single completely conserved residue G that may be functionally important.	2.85189e-24
NZ_CP042437.1|WP_147061096.1|6458571_6459207_+|DUF4291-family-protein	gnl|CDD|379483	pfam14124, DUF4291, Domain of unknown function (DUF4291). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and eukaryotes. Proteins in this family are typically between 190 and 214 amino acids in length. There are two conserved sequence motifs: VYQAY and RMTW.	8.39981e-89
NZ_CP042437.1|WP_147061097.1|6461060_6461477_+|transposase	gnl|CDD|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	2.69223e-07
NZ_CP042437.1|WP_147058934.1|6443347_6444025_-|response-regulator	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	4.84088e-69
NZ_CP042437.1|WP_147058962.1|6461587_6461863_-|UBP-type-zinc-finger-domain-containing-protein	gnl|CDD|366940	pfam02148, zf-UBP, Zn-finger in ubiquitin-hydrolases and other protein.	1.13161e-08
NZ_CP042437.1|WP_147058948.1|6451537_6452053_+|DUF2911-domain-containing-protein	gnl|CDD|378565	pfam11138, DUF2911, Protein of unknown function (DUF2911). This bacterial family of proteins has no known function.	3.18388e-58
NZ_CP042437.1|WP_147058952.1|6454417_6456610_+|acylase	gnl|CDD|376618	pfam01804, Penicil_amidase, Penicillin amidase. Penicillin amidase or penicillin acylase EC:3.5.1.11 catalyzes the hydrolysis of benzylpenicillin to phenylacetic acid and 6-aminopenicillanic acid (6-APA) a key intermediate in the the synthesis of penicillins. Also in the family is cephalosporin acylase and aculeacin A acylase which are involved in the synthesis of related peptide antibiotics.	6.6359e-118
NZ_CP042437.1|WP_147058956.1|6457521_6458505_+|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.	4.1022e-16
NZ_CP042437.1|WP_147058958.1|6459636_6460068_+|DoxX-family-membrane-protein	gnl|CDD|311556	pfam07681, DoxX, DoxX. These proteins appear to have some sequence similarity with pfam04173 but their function is unknown.	0.00026147
NZ_CP042437.1|WP_147058941.1|6447576_6448206_-|DUF47-family-protein	gnl|CDD|224310	COG1392, COG1392, Phosphate transport regulator (distant homolog of PhoU) [Inorganic ion transport and metabolism].	1.5261e-21
NZ_CP042437.1|WP_147058936.1|6444293_6444707_+|EamA-family-transporter	gnl|CDD|225308	COG2510, COG2510, Predicted membrane protein [Function unknown].	5.83384e-42
NZ_CP042437.1|WP_147058950.1|6452631_6453714_+|DUF3810-family-protein	gnl|CDD|378933	pfam12725, DUF3810, Protein of unknown function (DUF3810). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 333 and 377 amino acids in length. There is a conserved HEXXH sequence motif that is characteristic of metallopeptidases. This family may therefore belong to an as yet uncharacterized family of peptidase enzymes.	6.22425e-104
NZ_CP042437.1|WP_147058964.1|6461872_6463534_-|FAD-dependent-oxidoreductase	gnl|CDD|381126	cd17595, REC_TrxB, phosphoacceptor receiver (REC) domain a fused response regulator with a thioredoxin reductase output domain. This family is composed of uncharacterized fusion proteins containing a REC domain and a thioredoxin reductase domain. Thioredoxin reductase catalyzes the reduction of thioredoxin and is thus a central component in the thioredoxin system. Fusion proteins containing REC and thioredoxin reductase domains could play an important role in the environmental regulation of the cellular dithiol-disulfide ratio. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.86024e-82

Protein sequences

>NZ_CP042437.1|WP_147058950.1|6452631_6453714_+|DUF3810-family-protein
MRSYFNKNPFLKRITAILLLALAIFLLMLLAGYPALVERYYSQGFYKLICWVFHPVFNLFPFSVGDLLYTAIILAIVLAIIRMVKLLVKKQFKKIGLQLLGWIISIQVAVVAFYLFWGMNYFRPSAAVRLNLRDTTFTTADLKAVTKLLIDSANACRARVTAADLAQSNSTIYQTAVNAVKALSVDSANFRAFQPAIKPSMITFLLNYIGTSGYYNPFTSEAQINYAMPVFNRPFVACHEMSHQIGYGAEDEADFAGFIIAIKSKDRLLRYSGYHLAVDEFMHTLRRRDTLAHKELKAMVSKQVHQDFVTERAYWMAYENQLSWISSIFYDNFLKANNQPRGLATYNRMVLLVMAKYNVH
>NZ_CP042437.1|WP_147058948.1|6451537_6452053_+|DUF2911-domain-containing-protein
MNKPFQFKAAFVFAFALFLSSLAFAQEKPASPHDSTSATVAGSLIKIKYGSPYVKGRKILGELVPFDKVWRAGADSATSFTTSKAIKVQGKALPAGRYAFFVIPSASGTWTIIFDKNPKQWGAYTYKPENDQLRVTVKGKTAPKAESLTYTITPKGFNLKWDTFVVPVAIK
>NZ_CP042437.1|WP_147058946.1|6448909_6451288_+|TonB-dependent-receptor-plug-domain-containing-protein
MKKIVPALFCALCFCAPAFSQDAKAPLSLDGIVSRLQTLSTTKAIEKVYLHFDRTTYSAGDTAFFKAYLTLGEQHQLSKLSGVLHADLVNPNDSLVKYITLQVNNGLAWGDFPLPNSLPKGIYHIKAYTKWMLNSADPNVFDQPIIITSPVLPTRVLSAQQTKIANKYDIQFFPEGGTFVNDIPAKLAFKAIDHNGMGASVKGVVVDNLNAEITKFETRHLGMGIINITPVEGRTYKAKLTYADGTNATVDLPKADEKGMALLVNNTNPDKLLIEINANRAYYLANKNKEIGIAIYSGGGAVRSVKTTLDGQVLDLNLGKKDFQTGIVRVTLFSQTGEPMNERLSFIQNDDLMNLQTAVNKSSYTTREKVHLTLNAKKDDKPVVGYFSASVIDATKIPVDESAETTILTHLLLTSDLKGFVEQPNYYFNRVTNDTRADLDVLMLTQGYRRFEWKQLLGNDETTALAYPVERGLDISGTVKANSGTPVANGNVTLLAKNGGSMLTQVTDANGRFNFPNLAYSDNTPFVIQAKTADGKNNIQIIMDQPKELTLTLDNNKLAGGNNMEKSDGKTAPASVYMADASGKLLKEVIVKDKYLESHTNTITDFADQSGLGRSLEGRLPGVSLTNGVPYLRERVGISEAGPMLVIIDGVQGGSITDLNVSDVESVKMLKNVDAAIYGFQGSNGVLVITTKKNKGQAVNKKLSPGLITYAPKGFYKARTFYSPAYGGSVKQANKADDRVTIYWNPDVVTDKDGSASFDFYNADGKGNYRVIIEGIDDNGNVGRSVYTYKVE
>NZ_CP042437.1|WP_147058944.1|6448495_6448699_+|hypothetical-protein
MKPADKHYKFINSKTGYAIYYHSLSSDLNATEIKNQLQDIKARVAIQNGIYLETVYWEEIKENAEIQ
>NZ_CP042437.1|WP_147058941.1|6447576_6448206_-|DUF47-family-protein
MSIFPNSNQVFYDLFNRAVDNATQMATLLNTAVNSTDTYEQKFQFTHIDKLKTKSYEITHQVFTESGRTLISPFQRKDMCELAAAIDDVADSIAMASRRINLYDVPKITPPIINLANLILQTTQALESAVKAMNNLGNSAHIFEICNSIKQLEYQADTVYNEAFADLLANETDAIQLIKYTDVFMAMETATDSCEDATLIIESILIKNG
>NZ_CP042437.1|WP_158642994.1|6444966_6447438_+|TonB-dependent-receptor
MKTRYILLLLFVLVTINAWAQAPAPKGKISGKVTDAATKQPVDYATISVYKQGVAAPFNGISTDPKGNFTVDQIPPGEYRITADFLGYQRTTVDHVIVKAGGTTNLGEVLLSPNTHQLKDVTVTATTPTVQNKIDKMVYNPQNDLSAQGGVAIDILKKVPQITVDIDGNVELQGNANIRFLINGKPSSIFGASLADALASIPASQIKSIEVVTSPGAKYDAAGTGGIINIILKDSRVEGVNGSVNLSAGTRRENGSFNLNMRKGNFGVNAFFSGNAQINSNAPNTSNRTSTDGLGNTTTLFQQGSNNFKRNGYQSGLNFTWNISKHDDLTASVGFNHFGNHGSGLTNQDENKVDPNGIELSDIKTLRTSSSKFSGTSTDVSLAYKKTFEKEGQELDILYSSSFGNNSFSSSQLLQNLQAGTIPTGITNNNPGKDKETNISVDYTHPVSKNFTIETGGKLDFNHINNNVVTDTLLNGANVPNYNQTYGFTYDRKIYAYYLSLTTSVFNNFLDIKAGLRDEYTVTTADFKNTNIPNYNILVPSLVFSHKISESQSVKLSYTRRIERPDYGDLNPFLNISDTHNISTGDPNLKPERGDNFELGYNKSFDGGANINIAAFYRKNTDDLQRFTTFYDTLTIDGSTYTNVSLTKRYNLGSEEREGVNIYASVPITKAFNLRTNMIFSNRTSNNPGSPSVSGFTYRLNLNAQYNFGHDLSAEFFGNYNSSQRSIQGTQPKFVFYNIAMRKMFMNKKASIGLTASNPFAKYVSQSSTTYGTGFNQTNIRYVPIQSFGISLSYKFGKLEFKKDREKDDNGGKQDDMPADKGK
>NZ_CP042437.1|WP_147058936.1|6444293_6444707_+|EamA-family-transporter
MWWIYALLSALFAALTAIFAKIGIKGVDTDLATAIRTVVILILAWAIVLFKGSNQGISGLTKTNWTFLILSGCATGLSWICYFRALQLGKVSQVAPVDKLSVALAIVLAVVFLGEPLTLKNGIGALLIIAGTLVLIF
>NZ_CP042437.1|WP_147058934.1|6443347_6444025_-|response-regulator
MKLLIIEDEEGLRESIEEYFTEAGNICETAATYSAAISKIEMYSYDCILLDITLPGGNGINILKRLKDNNHQDGVLIISAKNSLDDRLQGLDLGADDYLVKPFHLSELKARVSAIIRRKMYNGSNLLTFNEISIDLQAKTVSVHDKSLKFTRKEFALLIYFIANKGKVVSKNAIAEHLWGDGIDLADNFDFIYSHIKNIRKKLVEAGANDYIQAAYGMGYKFAGQ
>NZ_CP042437.1|WP_147058932.1|6442103_6443351_-|HAMP-domain-containing-histidine-kinase
MKLITLYNRVNIVTTIAVMLITGIIYYQAISWILIDQADKSLKVEEDEVFDYVKLNKQLPQVFESKDQQISFTSAAPNSVTREFIDTLYKKDKDEVESGRGLISSITVNGKYYKILIVESKVETEDLIQIIFTITFGLILFLLLVLLVANRLILNRLWQPFHAILKEMKLFNITDNKEITQTETRIDEFADLNQAATAMTIRAKHDYKELKTFTENASHELLTPIAVINSKLDTLIQSENFNDRQSKLLNDLYSAVARLSRLNQSLLLLVKIENRLLTDQQTINLKQLIDEMLLQMEDIFADKQITVTARLEDKEISGSRYLIEILLNNLIINAVRHNHAGGEIVIDLTTAALTIKNTGADEPLDVDKIFTRFHKSAQSDGSGLGLTISKQICQSLNFSLTYRYSKPYHTFCMFF
>NZ_CP042437.1|WP_147058930.1|6440537_6441773_-|TolC-family-protein
MKWFFGLLLFTVTCTAARAQTYTLDHYLELAKNNSPLLKDLRNQLAATQIDSLRLRAGLKPQVNANSNGYFAPVIGGYGYAGAITNVQTFSALLGVNKQIVGKRNLNAQLAGINLQRDSVNNTTILSVQDLNRTITTQYITAYGSLQQVKFNTDVVKLLTEEEGFLKKLTRNNVYKQSEYLAFLVTLKQQQLQLSQAQIQYKNDYATLSYLAGVADTSAAEIAEPVIQKTATAAESESIFFRQFKSDSLRLLNQRDLIDISYRPKANIFADGGFNTDFGAQPYKNFGTSIGFSITMPIYDGGQRKLMYKKLKLQQETHATNKAFFKTQYQQQIAQLNQQINENDNLINQIKEQIKYAESLIKVDTQLMQTGDVKIADLILAVNSYYTITNLLTQTTITRLQLVNQLNYWNK
>NZ_CP042437.1|WP_147058952.1|6454417_6456610_+|acylase
MKLNLIFILLFSSLFVSAQKINPQEIKRAGDLAKRVTIIRDNYGVPHIYGETDASVVFGLMYAQCEDNFKGIERNYLYQFGKQTEVDGENSLATDIQLQLIADSADAINDYKTSAPAFRKLLDAFADGINYYLYKHPEVKPKVFKHFEPWYALMFTDGSVAATETGGIKLDETKEFYINGGDKLGYVPNSRARAYEFVNERETGSNGFAISPSRSASGHALLYINPHVPFYFRSEVELVSEEGLHAYGAVTWGQFFIYQGFNKHCGWMHTSSYADVADLYAEKMAKKDGRWFYEYNGTLKPVTERKLVINIKKGDKLEQKTITGYYTHHGPVVGSRDGKWLALKANNRSYNALVESWQITKANNLAEYKKAMDLVSNATNATVYADDKGNTIFWYGNYIPKRDPKYDWSLPVDGSTTATEWQGVHRLSEIVTTTNPATGWIQNCNSTPYTDAGASSPDKSKYPAYMAPDGENYRAITAINILKNAEGLTLDGLIAKGYDHYLAAFDDLLPALFKAYDEAPDSVKYSISDVMKILKQWDRRTAANSVASSLAIEWGTAMLKLLPPPKTDQESTFITRRIKTLADKTPGNQQLELLSAVMKNLQSRFGTWQVQWGDMNRYQRPADGITFDDKLPSIPVGLTGSGFGQLPSFQSRTVNTLKRYGYSGNSFVAAVEFGPRIKAKSIMTGGQSFDATSKNFTDQAQGIIEGKFKDVLFYREDVLKHVSKSYHPGS
>NZ_CP042437.1|WP_147058954.1|6456651_6457140_+|hypothetical-protein
MKKFLFVALLCFCGANLFGQSITVNDLTNLTNLTNADAHKYLVLAKGFKKAYTQELDGNTIEHLSKTDAEKKQESVDIGVALKLSSGAILRTVTYKTARTEQIFHLISQAKSQGLPMKFQGADTINNIYQFDNDFFHIVMYISRDNTSGYVEVKQKEYVGFD
>NZ_CP042437.1|WP_147058956.1|6457521_6458505_+|TIM-barrel-protein
MENISRKKFIAAATMATAGMALGLNAKGLTLPKDSNISDTGQFSPAKIKVSIFSKHLHWLNYADMASLAADMGFDGVDLTVRPDGHVLPEHVATDLPKAVAAVERAGLKVHTIVTNIKSPDEKYTHDILKAASALGIKYYRMAWLDYDKNISIPDNLKAINKQFKALEAINRQYNMHGAYQNHSGELFGASVWDLWLGMDGTNPDFIGCQYDVRHATTEGADTWPTSIQTLMPRIKTTNVKDFYWDKKDGKWQVKSVPLGEGMVDFPKYFRILKEQKINSPMSLHCEYELGGAQDGAKQLTISRDAFTTAVKKDLATLRGWLKEYDL
>NZ_CP042437.1|WP_147061096.1|6458571_6459207_+|DUF4291-family-protein
MITELYQDSIQRLPKTGQHLLGHQTEDLIIVYQAYNHNIADFAVENQFLGGNHYSYSRMSWIKPNFLWMMYRCGWAEKENQERVLALWIQKTDLEKILGEAAISSFNPKYYESHAQWRAGLDQKEVRLQWDPDHDPYGNKLQRRAIQLGLKGKMLEAFGKRQIRKIEDVTNFVKLQKQLLDAGRLDELLVPFETAFKTTDAALNDRVGIEG
>NZ_CP042437.1|WP_147058958.1|6459636_6460068_+|DoxX-family-membrane-protein
MNVVHKIEHWGDTHHPKFLDLVRIALGVFLLLKGVAFMENTAYLRDLIESQDVVDLSPGVLMVLVYYVTFAHMIGGILITLGIFTRLASIFQIPIVLGAVFLTGIFKEPINTLEWPSVTALILLVMFTILGSGPISLDRYLEG
>NZ_CP042437.1|WP_147058960.1|6460266_6461184_+|IS4-family-transposase
MPKDNFFSGQPVFAQLLSLIPRHIVSKQSQKYSADRYCKSFMSYDHLVTMLYQGFFQCLSLRELVTGLQANRSRLLHLGLTNTPRRSTLSDANSRRPADFFAAAYHQLYRYFYGSLPDSRPSLKKLFIIDSTTISLFSNIMGGAGMSKSNGKRKGGIKAHVMIDAEHNLPCFTLLTEARHHDLVFLQEVQVPPGSIVVFDRAYTNYKQFEAWGAQGIAWVTRQKNDANYQLLSESPVSTYSSEQGVIADQSLLLDGIATGAKYPLSGPAGSFLRTLPPRKSSRSLPTSPLLRPNRSLLCIKNGGR
>NZ_CP042437.1|WP_147061097.1|6461060_6461477_+|transposase
MRARRVVFKDPATQKELAFITNEPTLAPEQIAALYKKRWQIELLFKRIKQRYPLRYFLGDNVNAIQIQVWSMLICDLLVQIVLSQVNKAGKRKWSYANLAAMVKHHLMTYINLMAFLFDPEKALLNYKPPEPTAATLF
>NZ_CP042437.1|WP_147058962.1|6461587_6461863_-|UBP-type-zinc-finger-domain-containing-protein
MQNDDEICQHLAAITDIKQPKDYLCEECIKTHSSWMHLRTCQTCGVTLCCDSSPNTHMTKHFEATGHPVVISAEPGERWLWCYVDDAVKGY
>NZ_CP042437.1|WP_147058964.1|6461872_6463534_-|FAD-dependent-oxidoreductase
MNRPIIFSIDDDQQVLRSISRDLRSQYSKEYKILSTTSAQEALETLTELKNGSDVVALFLCDQRMPEMEGVKFLEKAKKVFPDAKRVLLTAYSDTEAAIKAINDVQLDYYLMKPWDPPEEKLYPVINDLLADWHNSYIPEFVGIKLVGYQFSPQSHVIKDYLAGNLIPYRWLDIEKNVDAGTLLALNNLSTDCLPMVFFEDGSYLQKPSIQGIAAKLEKNTQTLTDVYDVVIIGAGPAGLAAAVYGASEGLKTLLIERKAPGGQAGTSSRIENYLGFPAGLSGADLTRRAITQAMRLGAEFLSPQSVSDIKQKDGYKTIILDDGPEIISRTVVITTGVDYRKLEVKGVENFTGAGIYYGAATTEASACTGKDVYVIGGGNSAGQAAMHLSKYATKVHIVIRREDLVATMSAYLITQISETPNIEVLGNTEIVEAHGGNCLEKLTLKNCITQETFTNKAAALYIFIGAKPYTDWIKLDIIKNNKDFIETGRELRSYESFNKVWKLKRDPFLLETSCSGIFAAGDVRAGAMNRVASAVGEGSMAISFVHKYLAEV
>NZ_CP042437.1|WP_147058966.1|6463730_6465131_-|GHKL-domain-containing-protein
MQEVTVSWLKSLEALEHVPDDQLQWLIDHSEYNTFEDGTMLNEPGKPMTGPHIIVEGSMRFYMLQSRGRRDFVAVGPGNITGYLPFSRGLVSKGFAEAIGELRVLSFPTERITEMIKNHFELTQALVHIMTNRVRDFTALQQQNEKMMALGKLSAGLAHELNNPASAIVRDSTSLSKHLQLVPEAIKGMFAIKMDSDQVDGVTNEMFKVLTAKDEGRLSLKQRTHREDEIGEWLDENEIENSYEIAESFVDFNFKVENLDALKSYIPKQFLSTIFNWMSNKLVAEKMIQDIQESSKRIAELVSSVKTFTHMDRGQDKQYADIHIGITNTLTMLGYKIRKGNITVVEDFDRTLPEVKALIGELNQVWTNLIDNALDAMQPAGKGILTIKTRRDREFVEVFIIDDGPGIPEDIQSQIFDPFFTTKEMGKGTGMGLEVVQRIVKQHRGSIKVKSTPGCTVFSVCFLIDG

Crispr_ID: NZ_CP042437_14

• CRISPR_ID: NZ_CP042437_14
• CRISPR_location: 7233363-7233495
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP042437_14

Consensus_repeat	Method
AAGAGTCAGGAATCAAGACA	PILER-CR

spacers of NZ_CP042437_14

>14.1|7233383|46|NZ_CP042437|PILER-CR
TGATCAATTCTGGTTGCCAATATATACAAAATGTTTTAAGAGAGGC
>14.2|7233449|27|NZ_CP042437|PILER-CR
AGCACAAATCTTCAGTAAATGTCTTAA

CRISPR arrays and Neighbor proteins around NZ_CP042437_14

CRISPR arrays

The CRISPR arrays of NZ_CP042437_14

>merge|NZ_CP042437|14|7233363-7233495|PILER-CR
AAGAGTCAGGAATCAAGACATGATCAATTCTGGTTGCCAATATATACAAAATGTTTTAAGAGAGGCAAGAGTCAAGAATCAAGGCAAGCACAAATCTTCAGTAAATGTCTTAAAAGAGTCAGGAATCGAGACC

>NZ_CP042437|14|3|7233363-7233495|PILER-CR
AAGAGTCAGGAATCAAGACA	TGATCAATTCTGGTTGCCAATATATACAAAATGTTTTAAGAGAGGC
AAGAGTCAAGAATCAAGGCA	AGCACAAATCTTCAGTAAATGTCTTAA
AAGAGTCAGGAATCGAGACC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP042437.1|WP_147060010.1|7236940_7237567_-|HAD-hydrolase-like-protein	unknown	unknown	gnl|CDD|223943
NZ_CP042437.1|WP_147059989.1|7224585_7226487_-|OmpA-family-protein	unknown	unknown	gnl|CDD|143586
NZ_CP042437.1|WP_147060003.1|7232814_7233342_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147060006.1|7235487_7235985_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147060019.1|7242804_7243710_-|prephenate-dehydratase	unknown	unknown	gnl|CDD|270349
NZ_CP042437.1|WP_147060014.1|7238905_7240000_-|chorismate-synthase	unknown	unknown	gnl|CDD|376510
NZ_CP042437.1|WP_147060004.1|7233678_7235082_+|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl|CDD|224220
NZ_CP042437.1|WP_147060018.1|7241570_7242698_-|3-deoxy-7-phosphoheptulonate-synthase	unknown	unknown	gnl|CDD|273577
NZ_CP042437.1|WP_147059991.1|7226526_7227150_-|radical-SAM-protein	unknown	unknown	gnl|CDD|223675
NZ_CP042437.1|WP_090650785.1|7236419_7236809_+|50S-ribosomal-protein-L27	unknown	unknown	gnl|CDD|235464
NZ_CP042437.1|WP_147060012.1|7237563_7238805_-|MFS-transporter	unknown	unknown	gnl|CDD|340887
NZ_CP042437.1|WP_147060008.1|7236060_7236369_+|50S-ribosomal-protein-L21	unknown	unknown	gnl|CDD|235510
NZ_CP042437.1|WP_147061115.1|7223871_7224426_-|carbohydrate-binding-protein	unknown	unknown	gnl|CDD|271146
NZ_CP042437.1|WP_147059997.1|7228646_7229528_-|bifunctional-5,10-methylene-tetrahydrofolate-dehydrogenase/5,10-methylene-tetrahydrofolate-cyclohydrolase	unknown	unknown	gnl|CDD|184556
NZ_CP042437.1|WP_147060001.1|7232271_7232769_-|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl|CDD|224511
NZ_CP042437.1|WP_147060016.1|7240162_7241479_-|3-phosphoshikimate-1-carboxyvinyltransferase	unknown	unknown	gnl|CDD|238797
NZ_CP042437.1|WP_147059993.1|7227366_7228131_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147059999.1|7229627_7231415_-|elongation-factor-4	unknown	unknown	gnl|CDD|235462
NZ_CP042437.1|WP_090650382.1|7231694_7232285_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP042437.1|WP_147059995.1|7228134_7228473_+|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl|CDD|225057

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP042437.1|WP_147060010.1|7236940_7237567_-|HAD-hydrolase-like-protein	gnl|CDD|223943	COG1011, COG1011, Predicted hydrolase (HAD superfamily) [General function prediction only].	2.61482e-16
NZ_CP042437.1|WP_147059989.1|7224585_7226487_-|OmpA-family-protein	gnl|CDD|143586	cd07185, OmpA_C-like, Peptidoglycan binding domains similar to the C-terminal domain of outer-membrane protein OmpA. OmpA-like domains (named after the C-terminal domain of Escherichia coli OmpA protein) have been shown to non-covalently associate with peptidoglycan, a network of glycan chains composed of disaccharides, which are crosslinked via short peptide bridges. Well-studied members of this family include the Escherichia coli outer membrane protein OmpA, the Escherichia coli lipoprotein PAL, Neisseria meningitdis RmpM, which interact with the outer membrane, as well as the Escherichia coli motor protein MotB, and the Vibrio flagellar motor proteins PomB and MotY, which interact with the inner membrane.	8.33002e-45
NZ_CP042437.1|WP_090650785.1|7236419_7236809_+|50S-ribosomal-protein-L27	gnl|CDD|235464	PRK05435, rpmA, 50S ribosomal protein L27; Validated.	2.44549e-55
NZ_CP042437.1|WP_147060014.1|7238905_7240000_-|chorismate-synthase	gnl|CDD|376510	pfam01264, Chorismate_synt, Chorismate synthase.	0
NZ_CP042437.1|WP_147060004.1|7233678_7235082_+|cation:dicarboxylase-symporter-family-transporter	gnl|CDD|224220	COG1301, GltP, Na+/H+-dicarboxylate symporters [Energy production and conversion].	8.66883e-119
NZ_CP042437.1|WP_147060018.1|7241570_7242698_-|3-deoxy-7-phosphoheptulonate-synthase	gnl|CDD|273577	TIGR01361, DAHP_synth_Bsub, 3-deoxy-7-phosphoheptulonate synthase. This model describes one of at least three types of phospho-2-dehydro-3-deoxyheptonate aldolase (DAHP synthase). This enzyme catalyzes the first of 7 steps in the biosynthesis of chorismate, that last common precursor of all three aromatic amino acids and of PABA, ubiquinone and menaquinone. Some members of this family, including an experimentally characterized member from Bacillus subtilis, are bifunctional, with a chorismate mutase domain N-terminal to this region. The member of this family from Synechocystis PCC 6803, CcmA, was shown to be essential for carboxysome formation. However, no other candidate for this enzyme is present in that species, chorismate biosynthesis does occur, other species having this protein lack carboxysomes but appear to make chorismate, and a requirement of CcmA for carboxysome formation does not prohibit a role in chorismate biosynthesis. [Amino acid biosynthesis, Aromatic amino acid family].	1.84638e-50
NZ_CP042437.1|WP_147059991.1|7226526_7227150_-|radical-SAM-protein	gnl|CDD|223675	COG0602, NrdG, Organic radical activating enzymes [Posttranslational modification, protein turnover, chaperones].	1.29292e-42
NZ_CP042437.1|WP_147060019.1|7242804_7243710_-|prephenate-dehydratase	gnl|CDD|270349	cd13631, PBP2_Ct-PDT_like, Catalytic domain of prephenate dehydratase from Chlorobium tepidum and similar proteins, subgroup 2; the type 2 periplasmic binding protein fold. Prephenate dehydratase (PDT, EC:4.2.1.51) converts prephenate to phenylpyruvate through dehydration and decarboxylation reactions. PDT plays a key role in the biosynthesis of L-Phe in organisms that utilize the shikimate pathway. PDT is allosterically regulated by L-Phe and other amino acids. The catalytic PDT domain consists of two similar subdomains with a cleft in between, which hosts the highly conserved active site. In gram-postive bacteria and archaea, PDT is a monofunctional enzyme, consisting of a catalytic domain (PDT domain) and a regulatory domain (ACT) (aspartokinase, chorismate mustase domain). In gram-negative bacteria, PDT exists as fusion protein with chorismate mutase (CM), forming a bifunctional enzyme, P-protein (PheA). The CM in the P-protein catalyzes the pericycle isomerization of chorismate to prephenate that serves as a substrate for PDT. The CM and PDT are essentail enzymes for the biosynthesis of aromatic amino acids in microorganisms but are not found in humans. Thus, both CM and PDT can potentially serve as drug targets against microbial pathogens. The PDT domain has the same structural fold as the type 2 periplasmic binding proteins (PBP2), many of which are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	2.78082e-87
NZ_CP042437.1|WP_147060012.1|7237563_7238805_-|MFS-transporter	gnl|CDD|340887	cd17329, MFS_MdtH_MDR_like, Multidrug resistance protein MdtH and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of Escherichia coli MdtH and similar multidrug resistance (MDR) transporters from bacteria and archaea, many of which remain uncharacterized. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. MdtH confers resistance to norfloxacin and enoxacin. MdtH-like MDR transporters belong to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.7134e-55
NZ_CP042437.1|WP_147060008.1|7236060_7236369_+|50S-ribosomal-protein-L21	gnl|CDD|235510	PRK05573, rplU, 50S ribosomal protein L21; Validated.	1.96869e-43
NZ_CP042437.1|WP_147061115.1|7223871_7224426_-|carbohydrate-binding-protein	gnl|CDD|271146	cd04080, CBM6_cellulase-like, Carbohydrate Binding Module 6 (CBM6); appended to glycoside hydrolase (GH) domains, including GH5 (cellulase). This family includes carbohydrate binding module 6 (CBM6) domains that are appended to several glycoside hydrolase (GH) domains, including GH5 (cellulase) and GH16, as well as to coagulation factor 5/8 carbohydrate-binding domains. CBM6s are non-catalytic carbohydrate binding domains that facilitate the strong binding of the GH catalytic modules with their dedicated, insoluble substrates. The CBM6s are appended to GHs that display a diversity of substrate specificities. For some members of this family information is available about the specific substrates of the appended GH domains. It includes the CBM domains of various enzymes involved in cell wall degradation including, an extracellular beta-1,3-glucanase from Lysobacter enzymogenes encoded by the gluC gene (its catalytic domain belongs to the GH16 family), the tandem CBM domains of Pseudomonas sp. PE2 beta-1,3(4)-glucanase A (its catalytic domain also belongs to GH16), and a family 6 CBM from Cellvibrio mixtus Endoglucanase 5A (CmCBM6) which binds to the beta1,4-beta1,3-mixed linked glucans lichenan, and barley beta-glucan, cello-oligosaccharides, insoluble forms of cellulose, the beta1,3-glucan laminarin, and xylooligosaccharides, and the CBM6 of Fibrobacter succinogenes S85 XynD xylanase, appended to a GH10 domain, and Cellvibrio japonicas Cel5G appended to a GH5 (cellulase) domain. GH5 (cellulase) family includes enzymes with several known activities such as endoglucanase, beta-mannanase, and xylanase, which are involved in the degradation of cellulose and xylans. GH16 family includes enzymes with lichenase, xyloglucan endotransglycosylase (XET), and beta-agarase activities. CBM6 is an unusual CBM as it represents a chimera of two distinct binding sites with different modes of binding: binding site I within the loop regions and binding site II on the concave face of the beta-sandwich fold. For CmCBM6 it has been shown that these two binding sites have different ligand specificities.	3.66052e-33
NZ_CP042437.1|WP_147059997.1|7228646_7229528_-|bifunctional-5,10-methylene-tetrahydrofolate-dehydrogenase/5,10-methylene-tetrahydrofolate-cyclohydrolase	gnl|CDD|184556	PRK14185, PRK14185, bifunctional methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase FolD.	1.68869e-156
NZ_CP042437.1|WP_147060001.1|7232271_7232769_-|sigma-70-family-RNA-polymerase-sigma-factor	gnl|CDD|224511	COG1595, RpoE, DNA-directed RNA polymerase specialized sigma subunit, sigma24 homolog [Transcription].	1.40633e-33
NZ_CP042437.1|WP_147060016.1|7240162_7241479_-|3-phosphoshikimate-1-carboxyvinyltransferase	gnl|CDD|238797	cd01556, EPSP_synthase, EPSP synthase domain. 3-phosphoshikimate 1-carboxyvinyltransferase (5-enolpyruvylshikimate-3-phosphate synthase) (EC 2.5.1.19) catalyses the reaction between shikimate-3-phosphate (S3P) and phosphoenolpyruvate (PEP) to form 5-enolpyruvylshkimate-3-phosphate (EPSP), an intermediate in the shikimate pathway leading to aromatic amino acid biosynthesis. The reaction is phosphoenolpyruvate + 3-phosphoshikimate = phosphate + 5-O-(1-carboxyvinyl)-3-phosphoshikimate. It is found in bacteria and plants but not animals. The enzyme is the target of the widely used herbicide glyphosate, which has been shown to occupy the active site. In bacteria and plants, it is a single domain protein, while in fungi, the domain is found as part of a multidomain protein with functions that are all part of the shikimate pathway.	4.07131e-103
NZ_CP042437.1|WP_147059999.1|7229627_7231415_-|elongation-factor-4	gnl|CDD|235462	PRK05433, PRK05433, GTP-binding protein LepA; Provisional.	0
NZ_CP042437.1|WP_147059995.1|7228134_7228473_+|Rieske-2Fe-2S-domain-containing-protein	gnl|CDD|225057	COG2146, {NirD}, Ferredoxin subunits of nitrite reductase and ring-hydroxylating dioxygenases [Inorganic ion transport and metabolism / General function prediction only].	1.60676e-16

Protein sequences

>NZ_CP042437.1|WP_147060003.1|7232814_7233342_-|hypothetical-protein
MTVTTYGLQHIKKEIQHLPHEQLSELLLRLARYKKENKELLAYLLFEAYDETSFIEKVKAEAGFMFSQLPALSYNAAKGMRKILRLLSKYTKFTGSKTAEIEFLLNFCSNYLEYADRRTSYKPIRLILTRQVEKVKTLIAKLHEDLQYDFADSYNALITDAEKKLNWFKKSDYLL
>NZ_CP042437.1|WP_147060001.1|7232271_7232769_-|sigma-70-family-RNA-polymerase-sigma-factor
MANKEAAFKEIYAANSKKIFHLCYGYTGDDDAANDLLQETFLKVWQNLDKFRNQAMISTWIYRIAVNTCLTYLRSEKRQAKDELTEQIAETKREEFSEKNEQVALLYKCISKLEESERIIITLVLDEVPYPEIAEVSGISEGNLRVKIYRIKQKLTELYNQYERL
>NZ_CP042437.1|WP_090650382.1|7231694_7232285_-|hypothetical-protein
MKDFDHLMSVWQGQPKQDQLSVDDVLKQVKKGIRGITNKLYWTIVAMVAVTVFAAIVTFFLAFKSGVTTAGILIVLLTMLMYLALTVRHYHILSKRDATINPAEYLDSLKEYQKTRSKITGWFYYIYILLISAGLALYFIEVLENSSLAFKIGTYSSITIWFLFTTFYLKPRMFKNEEEKLNLMIDRLVRLKEQFN
>NZ_CP042437.1|WP_147059999.1|7229627_7231415_-|elongation-factor-4
MEHIRNFCIIAHIDHGKSTLADRLLEYTNTITQRESQAQLLDDMDLERERGITIKSHAIQMDYELNGQKYILNLIDTPGHVDFSYEVSRSIAACEGALLIVDAAQGIQAQTISNLYLALENDLEIIPVLNKMDLPGAMPEEVKDQIVDLIGCKREEILAASGKTGMGVHDILRAIVERVPAPVGDPKAPLQALIFDSVFNSFRGIIAYFKVVNGEIRKGEKVKFVATEKQYLADEVGTLKLRPLAKDVIKTGDVGYIISGIKEAREVKVGDTITHVDRPCEIGIQGFEEVKPMVFAGIYPVDTEDYEELRESMAKLQLNDASLVFEPESSAALGFGFRCGFLGMLHMEIIQERLEREFNMTVITTVPNVSYIAHTTKGEPIIVNNPSDLPDPSKIDFVEEPYIKATIITKSEFVGPVMSLCIQKRGSITNQSYLTSDRVELVFEMPMGEIVFDFYDKLKTISKGYASFDYHQIGYRQSDLVRLDIRLNAEPVDALSSLIFRGNSYDFGKKICEKLKELLPRQQFEIIIQASIGAKIIARETVKALRKDVTAKCYGGDISRKRKLLEKQKKGKKRMRQVGNVEIPQSAFMAVLKLD
>NZ_CP042437.1|WP_147059997.1|7228646_7229528_-|bifunctional-5,10-methylene-tetrahydrofolate-dehydrogenase/5,10-methylene-tetrahydrofolate-cyclohydrolase
MQLLDGKYVSEKLKVEIAEAAAKILAETGRQPHLVAVLVGHDGGSETYVASKIKNCEKVGFKSTLVRFEDTVTEDELLKKVEELNADADIDGIIVQLPLPKHIDPEKVTERIDHRKDVDGFHPVNLGRMQRNLPSFIPATPYGITLMLKEYGIETAGKHCVVVGRSNIVGSPMSILMARNTTPGNCTVTICHSRTPDIKKFTLDADILIVAIGKKNFITADMVKDGVVVIDVGMNRETSALTKSGFKLYGDVDFENVAPKASWITPVPGGVGLMTIIGLLKNTLSSANKEVYS
>NZ_CP042437.1|WP_147059995.1|7228134_7228473_+|Rieske-2Fe-2S-domain-containing-protein
MNWYKIAEIKNTLEPFIKKVKAGNRSICLVGFEGKIYATAINCPHAGFDLSQGLCVKGKIVCPYHRYTYNLTTGKGGEGQNDFLETYAVDIRGDDIYVGINSFWDKVRQAFK
>NZ_CP042437.1|WP_147059993.1|7227366_7228131_+|hypothetical-protein
MKKLYVPIIFLALLCFSSCVDIEEHYDFKSDGSCNVAYGFDMSKAVSVLVNLVSDSLKQTPQFSLVKDTTLNFYNAMPDSTQQKMNAAEIELAKSSDLTVNMNLKKSIMKVAINHKAKDAADLKYYLQNVSKIALNSQISALSTGQNNSKTLDAKQMVAGQDYYSYEITPHRFYRIVDKIKFNAFLKKTKSTFMMAKAMLIDMPYKVVLNFAKPIKKLNNPKAVLSADRRSITLVTNMDEVIKNPSVMNLKIDF
>NZ_CP042437.1|WP_147059991.1|7226526_7227150_-|radical-SAM-protein
MAHQIPDDGTLLPLMEEFYTIQGEGYNTGKAAYFIRLGGCDVGCHWCDVKESWDAELHPLTAADQIVANASVHPSKAVVVTGGEPLIYNLDYLTTQLHERGIKTFIETSGAYPLSGDWDWICLSPKKFKAPTPQVAEHAHELKVIVFNKSDFEWAEYHAKMVSPDCKLYLQPEWSKSKEMTPLIVDYVMNNPQWEISLQTHKYLNIP
>NZ_CP042437.1|WP_147059989.1|7224585_7226487_-|OmpA-family-protein
MRIITVFALFLFISATAWSQQRQYSTKNSEAIKYFAQAGQNLDEHYYDDAIENLQKAIAEDSKFVEAHAQLADVLKMRHLYKQAIEEYLKVIQLNPEFNRSIYLRIGETEIFEAKYPQAQQHLEKYLTYPDLTPQNNALAQKLIADTKFSIQALQHPVPFKPINMGANINTADDEYLPVATADESMLIFTRKINKNEDFYKSLKVNGKWDTATYLSNRINTDQYNEGAQSISQDGKYLFFTGCNRPDGRGRCDIYIAQKRGDDWGKPFDLSPPINTPGWESQPSISADGRTLYFVSNKKGGYGGYDIWKSSLTDKGWGEPENMGPNINTSYDEQSPFIHADDSTFYFCSNGWPGLGNKDLFVSRLGKDGKWQKPQNLGYPINTNGDENGLTLTAYGNYAFFASDNLNGFGGYDIYTFELPASLRPHIVTYVKGNVNDIKTHEPLEAAVEIIDLQNNTPVYQDYSSANEGDFLATITSGKNYGLNISKSGYLFYSDNFSLVGYKEQKPFHIKALLSPIEIGNKVILKNIFFDTNKFDLQSDSKAELLKLVEFLNVNPTVHIEISGHTDNVGAVQFNQTLSENRAKSVYQYLVTNGIPAARLVYKGYGETQPIAPNTTDENKAKNRRTEFMIIAK
>NZ_CP042437.1|WP_147061115.1|7223871_7224426_-|carbohydrate-binding-protein
MQKLPGRLECEFYNTGGEGVAYHDSDSTNNGSGRLNPANGTFLNEFRMQEGVDISYTKAHDHIDDNPYNKVPRDMNKFYVGWTQPGEWINYTVKVSKSGTYTIGVLYTSNGDGAISIDVDGKDATAPMKIASTHDNQDTTAWRQWHHWNASDSIGSITLTKGIHVLKLHIVANGNMNLDYLNFK
>NZ_CP042437.1|WP_147060004.1|7233678_7235082_+|cation:dicarboxylase-symporter-family-transporter
MQKKSKLTLYIFIALIAGVIVGYIYNTNVINKINSNISVADARIKAIDKNLLSSADTTTEAFKSIKKLRQTEVKAQQENSTLREDKLEGFNILSKIFLNLIKMIVAPLVFTTLVVGVAKVGDIKAVGRIGGKTMLWFVSATLVSLLLGMLLVNLFEPGKTMHLPLPDSHLSTGIKKSALSLTEFIGHVFPSSFIKSMADNEILQIVVFSLFFGIATAAIGEQGKIVIKAMDAIAHVILKITGYVMKLAPVAVFGAITAVIAKQGLGVLSTYGIFIGEFYFSLVLLWLIIISAGFIVLRKPVFRLINNIKDAMLIAFSTSTSEAAYPKVLLELERFGCSNKIVSFVLPLGYSFNLDGSMMYMTFASLFLAQSYDIHLSFGHQLSMLLVLMLTSKGVAGVPRASLVVIAGTLSMFNIPEAGLFLLIGIDPLLDMGRSATNVLGNAMATAVVSKWEGELDGKQVERNADI
>NZ_CP042437.1|WP_147060006.1|7235487_7235985_+|hypothetical-protein
MSSTTKKIFLISTIVIPFLLYCFYYYGMMIKNAPYRYADFQSISMVYGPKDSLVNKFNSRTGDYQYINKRDSLVKMHVKLTDNDLLYLHHKAADLGFWDFPSNERGDTVKEKPVRYIIEFKYKTKTKRVVFDSNFQGDPKLIDANKQLIKEIDQSLTTAERRLKK
>NZ_CP042437.1|WP_147060008.1|7236060_7236369_+|50S-ribosomal-protein-L21
MYAIVSIAGQQFKVAKDQQIFVHRLQGDEGASIEFDSVLLAENEGSFKLGSDLKGAKVSAKIVSHLKGDKVIVFKKKRRKGYKKKNGHRQQFTKIEITGITL
>NZ_CP042437.1|WP_090650785.1|7236419_7236809_+|50S-ribosomal-protein-L27
MAHKKGAGSSRNGRESHSKRLGIKIFGGQPAIAGNIIVRQRGTKHNPGVNVGIGRDHTLFALAEGIVVFRKKADNRSYVSVVPATEAVAEVAAAPAVVEAAPVAEEAPKAKKAAAPKAKKADTEEAAAE
>NZ_CP042437.1|WP_147060010.1|7236940_7237567_-|HAD-hydrolase-like-protein
MKKAIILDLDNTIYPVSSISGNLFEAVFGFVDTLAEEIGAEEIEKAKAEMQRRPYQQVAEKFNFSETAKNKGLDLLKDLEYALPMRPYEEYKYISETPIDKYLVTTGFTKLQWSKIRLLGIEADFKGIYIVDPQISSETKKDIFTMIMSNNNYRPEELLVIGDDPESEIKAAGSLGIDTFLFDPEDRHADAVVTHSSKSLKDAVLVFM
>NZ_CP042437.1|WP_147060012.1|7237563_7238805_-|MFS-transporter
MLSQLIQSYKNAYYGLSKNSWYLSLVMLINRSGTMVVPFMSVYMIKQLHFTVIQSGWVMAFFGIGAFGGAFLGGKLTDKIGFYDVQVGALLLGGIQFIILGYQHTFISICILTFVLSVCNESFRPANSAAIAHYADNATRTRSYSLNRLAVNLGWAVGGGLGGVLASINYHLLFWVDGCTNISAAVLLLSLMPRSQIRKSVKNVTKAVKSAAAHTDGMFLMFIILNTLFSCCFYEFFITQPVFYVIKWHLDSSFIGFLMALNGILIVVIEMVLVHKLDGKRHPLTYISIGVLLSGITFVLLNILPHNAAIAVLIVVMITFGEIIAMPFMNSFWVSRTNNSNRGSYAAIYGMSWSAAQIIAPAVGARIITSGGFDSLWWVFAGICLFVSTGYYVMKKLIKKSEPIALTPVDNIL
>NZ_CP042437.1|WP_147060014.1|7238905_7240000_-|chorismate-synthase
MAGNSFGQVFRITTFGESHGEAIGVIIDGCPAQLVVDIDYIQGELDKRKPGQSKITTQRKEADTVRILSGVFEGKTTGTPIAMLIPNEDQRSKDYTHNVDVFRPSHADYTYQTKYGIRDHRGGGRSSARETAARVAAGALAKLLLKTQGIEIAAHVSSVGKIYAPNVEIKNVQAFIDEREKNIVRCADPATAEEMIAFIDGIRKDGDTVGGKVSCYIKNCPVGLGDPVFDKLHADLGKAMLSINAVHGFEFGSGFAGSEMRGSEHNDIFVKSHLGDITTITNYSGGIQGGISNGMPIEFKVAFKPVATIMKNQATIDSEGNAAEISGKGRHDPCVVPRAVPIVEAMAALVLADHWLRNRNSKLS
>NZ_CP042437.1|WP_147060016.1|7240162_7241479_-|3-phosphoshikimate-1-carboxyvinyltransferase
MAMQNIILSKSNKHIKGTVNLTGSKSECNRALIIEALSNGKVKVDNVSDSADSVLLAGILRKNQESRVKDQEVLAGGSDHGPSTIDHGLQTVDIGPAGTAMRFLTAYYAIQDDEVILTGSQRMKERPIGVLVDALTELGAHIGFEEQEGYPPIRLKGGFEQLSRQISIKGNISSQYITALLLIAARLPLGLELHIEGELTSRPYVEMTLAMLQTAGIRHTWTDNVIAIANQDFATTSLYIEPDWSAASYWYAIAALADEAEIFLTGLTAYSLQGDSVITEIMANFGITSQFKDGGVHLLKEAKPLSRKVFDMKECPDLAQTVIVVCAALGHEATFTGLETLKIKETDRVLALQTELAKMGVKLIEKGQVYKLDCSEKFIPERMFINTYHDHRMAMAFAPLALIVPQLEFENGPVVDKSYPAFWDDLEKQGFIVEEVTI
>NZ_CP042437.1|WP_147060018.1|7241570_7242698_-|3-deoxy-7-phosphoheptulonate-synthase
MKLNLNIQPLHTWIKTGKEPLVIAGPCSAETEDQLVATAHLLAQTGKISALRAGIWKPRTRPGEFEGIGSIGLEWLKRAKAETGLPTAIEVATGKHVEEALKAGVDILWVGARSTVNPFTVQEIADALRGVDVPVMVKNPVNPDLSLWIGALERINNAGITKLAAIHRGFSSYEKSAFRNEPMWDIAIALKTLAPELPIINDPSHISGNRDLIGYISQKALDLDMQGLMIESHIDPSVAWTDAKQQVTPAALADIIDHLALRKPEVRNAEVNDKLAELRNQIDKIDDLVIQKIAERMLIADKIGQHKKDNGITILQVGRWDEILQKRTNYAKALKLGGEFTEKLLELLHAESISRQTAIMNASEAGQAAEKLTHA
>NZ_CP042437.1|WP_147060019.1|7242804_7243710_-|prephenate-dehydratase
MKIEKPRVAIQGIRASFHEEAGLRYFGENAQMIECNSFKQTFEKLKNREADYVVMAIENSIAGSILPNYTLLLDYGFPVVGEIYLPIQLHLMALPGVKFEDVKYVTSHPIALRQCVDFFDEYPHLKIIESSDTAACAKRIRDEQLTDTVAIANSLAATLYGLDVLERRIESNKRNFTRFLILTHHDNMDKKPANKASLCFQVSNKVGALAKVLNIFAEEGLNMSKIQSMPILGKRNEYNFYVDVEWDEQKHYDNAIRQILKYTQNFNILGEYERHDDEPSVAPKPQRIDRGRRYINIRRNV

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP042437_10	10.1|4073822|30|NZ_CP042437|CRISPRCasFinder	4073822-4073851	30	NZ_CP042437.1	1236146-1236175	1	0.967

1. spacer 10.1|4073822|30|NZ_CP042437|CRISPRCasFinder matches to position: 1236146-1236175, mismatch: 1, identity: 0.967

catgacaacgctctttagtatgttatttcc	CRISPR spacer
catgacaacgctctttagtatgtcatttcc	Protospacer
***********************.******

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP042437_12	12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230729-6230757	29	MH617085	Microviridae sp. isolate ctjj553, complete genome	1312-1340	3	0.897
NZ_CP042437_12	12.27|6224655|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224655-6224684	30	NZ_CP044465	Acinetobacter schindleri strain HZE23-1 plasmid pHZE23-1-2, complete sequence	29917-29946	4	0.867
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	HG531805	Clostridium phage CDMH1 complete genome	33971-34000	4	0.867
NZ_CP042437_12	12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230729-6230757	29	MH617412	Microviridae sp. isolate cteb899, complete genome	1273-1301	4	0.862
NZ_CP042437_12	12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230729-6230757	29	MH617030	Microviridae sp. isolate ctbd804, complete genome	1234-1262	4	0.862
NZ_CP042437_12	12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230729-6230757	29	MK012486	Microviridae sp. isolate ctbj6, complete genome	2752-2780	4	0.862
NZ_CP042437_12	12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230729-6230757	29	MH617339	Microviridae sp. isolate ctjd540, complete genome	1303-1331	4	0.862
NZ_CP042437_2	2.1|1755532|30|NZ_CP042437|CRISPRCasFinder	1755532-1755561	30	HQ634193	Cyanophage P-RSM6 genomic sequence	163717-163746	5	0.833
NZ_CP042437_8	8.2|3121193|28|NZ_CP042437|CRISPRCasFinder	3121193-3121220	28	NZ_AP017565	Pseudanabaena sp. ABRG5-3 plasmid ABRG53e, complete sequence	55611-55638	5	0.821
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	NZ_LR134429	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 20	25593-25619	5	0.815
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP044540	Borrelia sp. CA690 plasmid lp17, complete sequence	666-695	5	0.833
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP044540	Borrelia sp. CA690 plasmid lp17, complete sequence	667-696	5	0.833
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	AP013648	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C99-MedDCM-OCT-S33-C45, *** SEQUENCING IN PROGRESS ***	915-944	5	0.833
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MK250028	Prevotella phage Lak-B9, complete genome	294-323	5	0.833
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MK250025	Prevotella phage Lak-B6, complete genome	261-290	5	0.833
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MK250022	Prevotella phage Lak-B3, complete genome	294-323	5	0.833
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MK250020	Prevotella phage Lak-B1, complete genome	274-303	5	0.833
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NC_024989	Clostridium botulinum plasmid pMI06-01 DNA, complete genome, strain: Miyagi2006-01	17214-17243	5	0.833
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NC_025002	Clostridium botulinum plasmid pTO08 DNA, complete genome, strain: Tochigi2008	17214-17243	5	0.833
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	MH616914	Inoviridae sp. isolate ctfh53, complete genome	4079-4108	5	0.833
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	MH319754	Marine virus AG-345-L05 Ga0172272_11 genomic sequence	123561-123590	5	0.833
NZ_CP042437_2	2.1|1755532|30|NZ_CP042437|CRISPRCasFinder	1755532-1755561	30	MN276049	Acinetobacter phage BS46, complete genome	18300-18329	6	0.8
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	KX501134	Phage DP-2017a isolate CA39E hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds	8161-8187	6	0.778
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	KX501136	Phage DP-2017a isolate CA40B hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds	8161-8187	6	0.778
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	KX501135	Phage DP-2017a isolate CA40A hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds	8161-8187	6	0.778
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	KX501137	Phage DP-2017a isolate CA40C hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds	8161-8187	6	0.778
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	KX501138	Phage DP-2017a isolate CA40D hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds	8161-8187	6	0.778
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	KX501139	Phage DP-2017a isolate CA40E hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds	8161-8187	6	0.778
NZ_CP042437_11	11.2|5590057|27|NZ_CP042437|CRISPRCasFinder	5590057-5590083	27	NC_021794	Cellulophaga phage phi18:3, complete genome	19904-19930	6	0.778
NZ_CP042437_12	12.3|6222833|30|NZ_CP042437|CRISPRCasFinder	6222833-6222862	30	MN379631	Chicken microvirus mg4_164, complete genome	50-79	6	0.8
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP044540	Borrelia sp. CA690 plasmid lp17, complete sequence	668-697	6	0.8
NZ_CP042437_12	12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223592-6223621	30	NZ_CP038863	Campylobacter jejuni strain SCJK2 plasmid unnamed1, complete sequence	992-1021	6	0.8
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	NZ_CP013122	Fusobacterium nucleatum subsp. polymorphum strain ChDC F306 plasmid unnamed1, complete sequence	3863-3892	6	0.8
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	AP013877	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C117A-MedDCM-OCT-S27-C30, *** SEQUENCING IN PROGRESS ***	33104-33133	6	0.8
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	CP033552	Acinetobacter nosocomialis strain 2014S01-097 plasmid p2014S01-097-2, complete sequence	29346-29375	6	0.8
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	AP013511	Uncultured Mediterranean phage uvMED DNA, complete genome, group G21, isolate: uvMED-CGR-C117A-MedDCM-OCT-S32-C49	14110-14139	6	0.8
NZ_CP042437_12	12.16|6223820|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223820-6223849	30	NZ_CP049159	Caballeronia sp. SBC1 plasmid pSBC1_3, complete sequence	98296-98325	6	0.8
NZ_CP042437_12	12.16|6223820|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223820-6223849	30	NZ_CP049319	Caballeronia sp. SBC2 plasmid pSBC2-3, complete sequence	341087-341116	6	0.8
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	NZ_CP032629	Lactococcus sp. 1JSPR-7 plasmid unnamed2, complete sequence	1633-1662	6	0.8
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	NC_014502	Gloeothece verrucosa PCC 7822 plasmid Cy782203, complete sequence	146138-146167	6	0.8
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	NC_014502	Gloeothece verrucosa PCC 7822 plasmid Cy782203, complete sequence	284888-284917	6	0.8
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	NZ_CP013122	Fusobacterium nucleatum subsp. polymorphum strain ChDC F306 plasmid unnamed1, complete sequence	3863-3892	6	0.8
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	AP013877	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C117A-MedDCM-OCT-S27-C30, *** SEQUENCING IN PROGRESS ***	33104-33133	6	0.8
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	CP033552	Acinetobacter nosocomialis strain 2014S01-097 plasmid p2014S01-097-2, complete sequence	29346-29375	6	0.8
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	AP013511	Uncultured Mediterranean phage uvMED DNA, complete genome, group G21, isolate: uvMED-CGR-C117A-MedDCM-OCT-S32-C49	14110-14139	6	0.8
NZ_CP042437_12	12.32|6225035|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225035-6225064	30	HM144385	Brochothrix phage NF5, complete genome	31983-32012	6	0.8
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NC_020394	Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-233, complete sequence	130807-130836	6	0.8
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	CP020755	Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-16, complete sequence	368235-368264	6	0.8
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NZ_CP021062	Bacillus thuringiensis strain ATCC 10792 plasmid poh1, complete sequence	583753-583782	6	0.8
NZ_CP042437_12	12.41|6225719|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225719-6225748	30	MN693703	Marine virus AFVG_250M594, complete genome	13650-13679	6	0.8
NZ_CP042437_12	12.52|6226554|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6226554-6226583	30	KJ019071	Synechococcus phage ACG-2014g isolate Syn7803US105, complete genome	19662-19691	6	0.8
NZ_CP042437_12	12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227160-6227189	30	NZ_CP018213	Lactobacillus plantarum strain BLS41 plasmid pLPBLS41_4, complete sequence	25055-25084	6	0.8
NZ_CP042437_12	12.62|6227311|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227311-6227340	30	NC_015583	Novosphingobium sp. PP1Y plasmid Mpl, complete sequence	990462-990491	6	0.8
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK893987	Staphylococcus phage PMBT8, complete genome	36760-36789	6	0.8
NZ_CP042437_12	12.93|6229667|30|NZ_CP042437|CRISPRCasFinder	6229667-6229696	30	NZ_AP022607	Mycobacterium branderi strain JCM 12687 plasmid pJCM12687	680279-680308	6	0.8
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	605697-605726	6	0.8
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	294881-294910	6	0.8
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP007513	Bacillus bombysepticus plasmid pBb, complete genome	412821-412850	6	0.8
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP050184	Bacillus thuringiensis strain HER1410 plasmid pLUSID1, complete sequence	114299-114328	6	0.8
NZ_CP042437_2	2.1|1755532|30|NZ_CP042437|CRISPRCasFinder	1755532-1755561	30	NZ_CP032095	Vibrio alfacsensis strain CAIM 1831 plasmid pVa1, complete sequence	136516-136545	7	0.767
NZ_CP042437_2	2.1|1755532|30|NZ_CP042437|CRISPRCasFinder	1755532-1755561	30	NZ_AP018256	Calothrix sp. NIES-4071 plasmid plasmid1 DNA, complete genome	110889-110918	7	0.767
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP020436	Bacillus sp. FDAARGOS_235 plasmid 2, complete sequence	10760-10789	7	0.767
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP014289	Bacillus thuringiensis strain Bt185 plasmid pBT1850046, complete sequence	33470-33499	7	0.767
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP047434	Spiroplasma citri strain BLH-13 plasmid pSciBLH13-6	36453-36482	7	0.767
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP047434	Spiroplasma citri strain BLH-13 plasmid pSciBLH13-6	36451-36480	7	0.767
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP033050	Virgibacillus halodenitrificans strain Bac324 plasmid unnamed, complete sequence	156925-156954	7	0.767
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP034710	Salmonella enterica subsp. enterica serovar Karamoja strain RSE21 plasmid pRSE21, complete sequence	4257-4286	7	0.767
NZ_CP042437_12	12.10|6223364|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223364-6223393	30	NC_012473	Bacillus cereus 03BB102 plasmid p03BB102_179, complete sequence	81704-81733	7	0.767
NZ_CP042437_12	12.10|6223364|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223364-6223393	30	NZ_CP009317	Bacillus cereus 03BB102 plasmid unnamed, complete sequence	55190-55219	7	0.767
NZ_CP042437_12	12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223516-6223545	30	NZ_CP045419	Pseudoalteromonas sp. THAF3 plasmid pTHAF3_a, complete sequence	728956-728985	7	0.767
NZ_CP042437_12	12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223516-6223545	30	HM152765	Mycobacterium phage Island3, complete genome	38184-38213	7	0.767
NZ_CP042437_12	12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223516-6223545	30	NC_011291	Mycobacterium phage Brujita, complete genome	38184-38213	7	0.767
NZ_CP042437_12	12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223592-6223621	30	CP016195	Bacillus thuringiensis serovar coreanensis strain ST7 plasmid pST7-1, complete sequence	42522-42551	7	0.767
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	KT962247	Cellulophaga phage phi17:2_18, complete genome	87626-87655	7	0.767
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	KT962246	Cellulophaga phage phi4:1_18, complete genome	87173-87202	7	0.767
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	KT962245	Cellulophaga phage phi4:1_13, complete genome	87173-87202	7	0.767
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	KC821632	Cellulophaga phage phi4:1, complete genome	87173-87202	7	0.767
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	NC_021798	Cellulophaga phage phi17:2, complete genome	87626-87655	7	0.767
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	KT962247	Cellulophaga phage phi17:2_18, complete genome	87626-87655	7	0.767
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	KT962246	Cellulophaga phage phi4:1_18, complete genome	87173-87202	7	0.767
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	KT962245	Cellulophaga phage phi4:1_13, complete genome	87173-87202	7	0.767
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	KC821632	Cellulophaga phage phi4:1, complete genome	87173-87202	7	0.767
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	NC_021798	Cellulophaga phage phi17:2, complete genome	87626-87655	7	0.767
NZ_CP042437_12	12.33|6225111|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225111-6225140	30	NZ_CP025980	Escherichia marmotae strain HT073016 plasmid pEM148, complete sequence	42538-42567	7	0.767
NZ_CP042437_12	12.33|6225111|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225111-6225140	30	LC425522	Uncultured phage DNA, contig: NODE620	7593-7622	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NC_048665	Clostridium phage phiCDHM14, complete genome	19939-19968	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	HG796225	Clostridium phage phiCDHM13 complete genome	19439-19468	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	HG798901	Clostridium phage phiCDHM11 complete genome	19438-19467	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MK473382	Clostridium phage JD032, complete genome	14451-14480	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MN693097	Marine virus AFVG_25M78, complete genome	37010-37039	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MH552526	Siphoviridae sp. isolate ctfj46, complete genome	36161-36190	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NC_002669	Lactococcus prophage bIL310, complete genome	167-196	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	MK774614	Aeromonas phage CF8, complete genome	35557-35586	7	0.767
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	AF323671	Bacteriophage bIL310, complete genome	167-196	7	0.767
NZ_CP042437_12	12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225339-6225368	30	NC_023917	Clostridium perfringens plasmid pCP-OS1 DNA, complete sequence, strain: OS1	20389-20418	7	0.767
NZ_CP042437_12	12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225339-6225368	30	NC_023918	Clostridium perfringens plasmid pCP-TS1 DNA, complete sequence, strain: TS1	20371-20400	7	0.767
NZ_CP042437_12	12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225339-6225368	30	NC_011255	Borrelia recurrentis A1 plasmid pl35, complete sequence	21330-21359	7	0.767
NZ_CP042437_12	12.51|6226478|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6226478-6226507	30	NZ_CP019737	Lactobacillus brevis strain TMW 1.2108 plasmid pl12108-3, complete sequence	39550-39579	7	0.767
NZ_CP042437_12	12.51|6226478|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6226478-6226507	30	NZ_CP019746	Lactobacillus brevis strain TMW 1.2111 plasmid pl12111-3, complete sequence	42716-42745	7	0.767
NZ_CP042437_12	12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227160-6227189	30	NC_049968	Bacillus phage DK2, complete genome	16094-16123	7	0.767
NZ_CP042437_12	12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227160-6227189	30	MK284528	Bacillus phage DK3, complete genome	16782-16811	7	0.767
NZ_CP042437_12	12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227160-6227189	30	MK284526	Bacillus phage DK1, complete genome	16644-16673	7	0.767
NZ_CP042437_12	12.63|6227387|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227387-6227416	30	MK552327	Pseudomonas phage Psa21, complete genome	151402-151431	7	0.767
NZ_CP042437_12	12.71|6227995|30|NZ_CP042437|CRISPRCasFinder	6227995-6228024	30	NZ_CP045607	Bacillus cereus strain SB1 plasmid p1, complete sequence	226421-226450	7	0.767
NZ_CP042437_12	12.71|6227995|30|NZ_CP042437|CRISPRCasFinder	6227995-6228024	30	LR134127	Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7	129601-129630	7	0.767
NZ_CP042437_12	12.71|6227995|30|NZ_CP042437|CRISPRCasFinder	6227995-6228024	30	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	663-692	7	0.767
NZ_CP042437_12	12.71|6227995|30|NZ_CP042437|CRISPRCasFinder	6227995-6228024	30	NZ_CP014283	Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence	7751-7780	7	0.767
NZ_CP042437_12	12.71|6227995|30|NZ_CP042437|CRISPRCasFinder	6227995-6228024	30	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	325364-325393	7	0.767
NZ_CP042437_12	12.71|6227995|30|NZ_CP042437|CRISPRCasFinder	6227995-6228024	30	NZ_CP032614	Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence	332461-332490	7	0.767
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NZ_CP048619	Legionella pneumophila strain ERS1305867 plasmid unnamed, complete sequence	96-125	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	NZ_CP041669	Legionella israelensis strain L18-01051 plasmid unnamed, complete sequence	62436-62465	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448514	Streptococcus satellite phage Javan480, complete genome	2514-2543	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448347	Streptococcus satellite phage Javan171, complete genome	2514-2543	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448508	Streptococcus satellite phage Javan466, complete genome	2980-3009	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448346	Streptococcus satellite phage Javan168, complete genome	4254-4283	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448344	Streptococcus satellite phage Javan165, complete genome	4254-4283	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448339	Streptococcus satellite phage Javan154, complete genome	3506-3535	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448329	Streptococcus satellite phage Javan134, complete genome	10533-10562	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448325	Streptococcus satellite phage Javan125, complete genome	10533-10562	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448326	Streptococcus satellite phage Javan127, complete genome	3996-4025	7	0.767
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	MK448335	Streptococcus satellite phage Javan148, complete genome	10533-10562	7	0.767
NZ_CP042437_12	12.77|6228451|30|NZ_CP042437|CRISPRCasFinder	6228451-6228480	30	MH572451	Microviridae sp. isolate SD_MC_7, complete genome	173-202	7	0.767
NZ_CP042437_12	12.78|6228527|30|NZ_CP042437|CRISPRCasFinder	6228527-6228556	30	MN694130	Marine virus AFVG_250M413, complete genome	21409-21438	7	0.767
NZ_CP042437_12	12.87|6229211|30|NZ_CP042437|CRISPRCasFinder	6229211-6229240	30	NZ_CP019972	Enterococcus faecium isolate 2014-VREF-114 plasmid p114-2 sequence	114631-114660	7	0.767
NZ_CP042437_12	12.91|6229515|30|NZ_CP042437|CRISPRCasFinder	6229515-6229544	30	NZ_CP021406	Celeribacter manganoxidans strain DY25 plasmid pDY25-B, complete sequence	54499-54528	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP021449	Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence	528080-528109	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	CP023013	Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence	539789-539818	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP049790	Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence	1534131-1534160	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP049794	Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence	1137718-1137747	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP049788	Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence	1377128-1377157	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP021763	Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence	643477-643506	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP015116	Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence	703547-703576	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP049792	Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence	919194-919223	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP016915	Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence	107309-107338	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	783416-783445	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP015851	Ralstonia solanacearum strain YC40-M plasmid, complete sequence	1635143-1635172	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP022783	Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence	541277-541306	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP022795	Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence	540372-540401	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP009763	Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence	545616-545645	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	CP023015	Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence	1448162-1448191	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052085	Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence	605752-605781	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052095	Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence	550185-550214	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	643494-643523	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052077	Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence	538324-538353	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052087	Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence	605752-605781	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052097	Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence	550185-550214	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052127	Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence	605752-605781	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052079	Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence	538328-538357	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052089	Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence	605756-605785	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052093	Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence	550185-550214	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052101	Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence	550185-550214	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052099	Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence	550185-550214	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052125	Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence	538328-538357	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052129	Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence	548696-548725	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052123	Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence	538328-538357	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052131	Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence	605752-605781	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052081	Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence	538328-538357	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052083	Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence	538328-538357	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052091	Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence	550187-550216	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052111	Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence	1524029-1524058	7	0.767
NZ_CP042437_12	12.92|6229591|30|NZ_CP042437|CRISPRCasFinder	6229591-6229620	30	NZ_CP052113	Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence	1524029-1524058	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	JQ182733	Enterobacterial phage mEp213, complete genome	43673-43702	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	JQ182730	Enterobacteria phage mEp237, complete genome	43857-43886	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	NC_019706	Enterobacteria phage mEp043 c-1, complete genome	42333-42362	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	KM389288	UNVERIFIED: Escherichia phage Phi06_2987 S clone contig00002 genomic sequence	304-333	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	NC_011892	Methylobacterium nodulans ORS 2060 plasmid pMNOD01, complete sequence	401404-401433	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	AP014139	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C47-MedDCM-OCT-S39-C56, *** SEQUENCING IN PROGRESS ***	8499-8528	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	NZ_CP028348	Novosphingobium sp. THN1 plasmid pTHN, complete sequence	79008-79037	7	0.767
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	AP014138	Uncultured Mediterranean phage uvMED isolate uvMED-GF-C47-MedDCM-OCT-S36-C43, *** SEQUENCING IN PROGRESS ***	23589-23618	7	0.767
NZ_CP042437_12	12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230273-6230302	30	NC_019542	Pectobacterium phage PP1, complete genome	12727-12756	7	0.767
NZ_CP042437_12	12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230273-6230302	30	KY744566	Pectobacterium phage POP72, complete genome	11906-11935	7	0.767
NZ_CP042437_12	12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230653-6230682	30	NC_019542	Pectobacterium phage PP1, complete genome	12727-12756	7	0.767
NZ_CP042437_12	12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230653-6230682	30	KY744566	Pectobacterium phage POP72, complete genome	11906-11935	7	0.767
NZ_CP042437_2	2.1|1755532|30|NZ_CP042437|CRISPRCasFinder	1755532-1755561	30	MG592580	Vibrio phage 1.210.O._10N.222.52.C2, partial genome	46473-46502	8	0.733
NZ_CP042437_7	7.1|2921874|35|NZ_CP042437|CRISPRCasFinder	2921874-2921908	35	MG592621	Vibrio phage 1.255.O._10N.286.45.F1, partial genome	81052-81086	8	0.771
NZ_CP042437_7	7.1|2921874|35|NZ_CP042437|CRISPRCasFinder	2921874-2921908	35	MG592609	Vibrio phage 1.244.A._10N.261.54.C3, partial genome	81052-81086	8	0.771
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP020436	Bacillus sp. FDAARGOS_235 plasmid 2, complete sequence	10762-10791	8	0.733
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NC_022879	Enterococcus mundtii QU 25 plasmid pQY182, complete sequence	171437-171466	8	0.733
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP043834	Bacillus sp. BS98 plasmid unnamed4	50781-50810	8	0.733
NZ_CP042437_12	12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223516-6223545	30	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	1087252-1087281	8	0.733
NZ_CP042437_12	12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223516-6223545	30	NZ_CP039641	Azospirillum sp. TSH100 plasmid p2, complete sequence	22191-22220	8	0.733
NZ_CP042437_12	12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223516-6223545	30	MT498036	Gordonia Phage Zitch, complete genome	50999-51028	8	0.733
NZ_CP042437_12	12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223592-6223621	30	NC_014633	Ilyobacter polytropus DSM 2926 plasmid pILYOP01, complete sequence	539809-539838	8	0.733
NZ_CP042437_12	12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223592-6223621	30	MT188223	Acinetobacter phage vB_AbaM_D22, complete genome	39836-39865	8	0.733
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	MK448705	Streptococcus phage Javan215, complete genome	13894-13923	8	0.733
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	L37090	Bacteriophage P001 (from Lactococcus lactis) gene, terminal region	1790-1819	8	0.733
NZ_CP042437_12	12.16|6223820|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223820-6223849	30	NZ_CP034168	Enterococcus avium strain 352 plasmid unnamed, complete sequence	7992-8021	8	0.733
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	MN694590	Marine virus AFVG_250M75, complete genome	9421-9450	8	0.733
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	MN694249	Marine virus AFVG_250M74, complete genome	26230-26259	8	0.733
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	MK448705	Streptococcus phage Javan215, complete genome	13894-13923	8	0.733
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	L37090	Bacteriophage P001 (from Lactococcus lactis) gene, terminal region	1790-1819	8	0.733
NZ_CP042437_12	12.26|6224579|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224579-6224608	30	MN693750	Marine virus AFVG_250M298, complete genome	7861-7890	8	0.733
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	NZ_CP049229	Lactobacillus iners strain C0210C1 plasmid pC0210C1, complete sequence	69556-69585	8	0.733
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	NZ_CP049227	Lactobacillus iners strain C0011D1 plasmid pC0011D1, complete sequence	78396-78425	8	0.733
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	CP002030	Campylobacter jejuni subsp. jejuni ICDCCJ07001 plasmid pTet, complete sequence	581-610	8	0.733
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	NZ_CP025619	Acinetobacter schindleri strain SGAir0122 plasmid pSGAir0122, complete sequence	55345-55374	8	0.733
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NZ_CP013709	Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence	53102-53131	8	0.733
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NZ_CP013844	Clostridium botulinum strain A634 plasmid pRSJ19_2, complete sequence	98540-98569	8	0.733
NZ_CP042437_12	12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225187-6225216	30	NC_009700	Clostridium botulinum F str. Langeland plasmid pCLI, complete sequence	11248-11277	8	0.733
NZ_CP042437_12	12.41|6225719|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225719-6225748	30	NZ_LR214999	Mycoplasma conjunctivae strain NCTC10147 plasmid 3	20064-20093	8	0.733
NZ_CP042437_12	12.41|6225719|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225719-6225748	30	LR214965	Mycoplasma fermentans strain NCTC10117 genome assembly, plasmid: 11	9655-9684	8	0.733
NZ_CP042437_12	12.47|6226175|29|NZ_CP042437|CRISPRCasFinder,PILER-CR	6226175-6226203	29	NZ_CP049297	Bacillus megaterium strain S188 plasmid pS188, complete sequence	121203-121231	8	0.724
NZ_CP042437_12	12.55|6226782|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6226782-6226811	30	NZ_CP033220	Parasedimentitalea marina strain W43 plasmid pW43A, complete sequence	39896-39925	8	0.733
NZ_CP042437_12	12.55|6226782|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6226782-6226811	30	NZ_CP033220	Parasedimentitalea marina strain W43 plasmid pW43A, complete sequence	121603-121632	8	0.733
NZ_CP042437_12	12.68|6227767|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227767-6227796	30	NZ_CP022999	Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence	1219191-1219220	8	0.733
NZ_CP042437_12	12.69|6227843|30|NZ_CP042437|CRISPRCasFinder	6227843-6227872	30	NZ_CP025552	Streptomyces rimosus strain WT5260 plasmid unnamed, complete sequence	187641-187670	8	0.733
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NZ_CP021282	Legionella pneumophila subsp. pneumophila strain Flint 2 (D-7477) plasmid unnamed, complete sequence	70731-70760	8	0.733
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NZ_CP016031	Legionella pneumophila strain OLDA plasmid unnamed, complete sequence	91029-91058	8	0.733
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NZ_LT598658	Legionella pneumophila strain Lpm7613 isolate Lpm7613 plasmid 2	127170-127199	8	0.733
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NZ_LN681226	Legionella hackeliae strain ATCC 35250 plasmid II, complete sequence	86167-86196	8	0.733
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NZ_CP021287	Legionella pneumophila subsp. pneumophila strain Albuquerque 1 (D-7474) plasmid unnamed, complete sequence	27592-27621	8	0.733
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NZ_CP004007	Legionella oakridgensis ATCC 33761 = DSM 21215 plasmid unnamed, complete sequence	815-844	8	0.733
NZ_CP042437_12	12.72|6228071|30|NZ_CP042437|CRISPRCasFinder	6228071-6228100	30	NC_006365	Legionella pneumophila str. Paris plasmid pLPP, complete sequence	817-846	8	0.733
NZ_CP042437_12	12.73|6228147|30|NZ_CP042437|CRISPRCasFinder	6228147-6228176	30	NZ_AP018204	Leptolyngbya boryana NIES-2135 plasmid plasmid1 DNA, complete genome	310144-310173	8	0.733
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	CP003185	Thermoanaerobacterium saccharolyticum JW/SL-YS485 plasmid pMU3262, complete genome	100533-100562	8	0.733
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	NC_019956	Thermoanaerobacterium thermosaccharolyticum M0795 plasmid pTHETHE01, complete sequence	49881-49910	8	0.733
NZ_CP042437_12	12.80|6228679|30|NZ_CP042437|CRISPRCasFinder	6228679-6228708	30	NZ_CP040048	Acinetobacter baumannii strain VB1190 plasmid unnamed1, complete sequence	632117-632146	8	0.733
NZ_CP042437_12	12.80|6228679|30|NZ_CP042437|CRISPRCasFinder	6228679-6228708	30	KY883640	Vibrio phage JSF17, complete genome	53112-53141	8	0.733
NZ_CP042437_12	12.84|6228983|30|NZ_CP042437|CRISPRCasFinder	6228983-6229012	30	NZ_CP021356	Rhodococcus sp. S2-17 plasmid pRB29, complete sequence	147507-147536	8	0.733
NZ_CP042437_12	12.89|6229363|30|NZ_CP042437|CRISPRCasFinder	6229363-6229392	30	MN035857	Leviviridae sp. isolate H2_Bulk_36_scaffold_96 hypothetical protein (H2Bulk3696_000001), hypothetical protein (H2Bulk3696_000002), and RNA-dependent RNA polymerase (H2Bulk3696_000003) genes, complete cds	1104-1133	8	0.733
NZ_CP042437_12	12.95|6229819|30|NZ_CP042437|CRISPRCasFinder	6229819-6229848	30	MN693433	Marine virus AFVG_25M397, complete genome	9717-9746	8	0.733
NZ_CP042437_12	12.95|6229819|30|NZ_CP042437|CRISPRCasFinder	6229819-6229848	30	AP018399	Xanthomonas phage XacN1 DNA, complete genome	82155-82184	8	0.733
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	NZ_CP034079	Pseudomonas syringae pv. pisi str. PP1 plasmid pPP1-1, complete sequence	16943-16972	8	0.733
NZ_CP042437_12	12.96|6229895|30|NZ_CP042437|CRISPRCasFinder	6229895-6229924	30	NZ_CP015623	Corynebacterium crudilactis strain JZ16 plasmid pCRULAC1, complete sequence	91358-91387	8	0.733
NZ_CP042437_12	12.97|6229971|29|NZ_CP042437|CRISPRCasFinder	6229971-6229999	29	LR134125	Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 5	585142-585170	8	0.724
NZ_CP042437_12	12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230273-6230302	30	MT496971	Escherichia phage Mt1B1_P10, complete genome	33157-33186	8	0.733
NZ_CP042437_12	12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230653-6230682	30	MT496971	Escherichia phage Mt1B1_P10, complete genome	33157-33186	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	AP022644	Bacillus wiedmannii PL1 plasmid pBwiPL1-1 DNA, complete sequence	309300-309329	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP012101	Bacillus thuringiensis strain HS18-1 plasmid pHS18-2, complete sequence	149930-149959	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP016596	Bacillus cereus strain K8 plasmid pBCM301, complete sequence	153135-153164	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP018741	Bacillus cereus strain FORC_047 plasmid pFORC47_1, complete sequence	35540-35569	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP029455	Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence	334777-334806	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP010112	Bacillus thuringiensis serovar indiana strain HD521 plasmid pBTHD521-6, complete sequence	290429-290458	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NC_018688	Bacillus thuringiensis MC28 plasmid pMC319, complete sequence	190688-190717	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP045608	Bacillus cereus strain SB1 plasmid p2, complete sequence	39548-39577	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP009336	Bacillus thuringiensis strain HD1011 plasmid 1, complete sequence	54066-54095	8	0.733
NZ_CP042437_12	12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230956-6230985	30	NZ_CP016590	Bacillus thuringiensis strain KNU-07 plasmid pBTKNU07-02, complete sequence	71864-71893	8	0.733
NZ_CP042437_12	12.112|6231108|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6231108-6231137	30	NC_011412	Clostridium perfringens plasmid pCP8533etx, complete sequence	46041-46070	8	0.733
NZ_CP042437_12	12.112|6231108|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6231108-6231137	30	NC_007773	Clostridium perfringens plasmid pCPF5603, complete sequence	43751-43780	8	0.733
NZ_CP042437_12	12.113|6231184|29|NZ_CP042437|CRISPRCasFinder,PILER-CR	6231184-6231212	29	MN694669	Marine virus AFVG_250M354, complete genome	11827-11855	8	0.724
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP014289	Bacillus thuringiensis strain Bt185 plasmid pBT1850046, complete sequence	33472-33501	9	0.7
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NC_007392	Spiroplasma citri plasmid pSci6	1821-1850	9	0.7
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NC_018146	Zymomonas mobilis subsp. mobilis ATCC 29191 plasmid pZZ6.01, complete sequence	10852-10881	9	0.7
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	MF974396	Leptospira phage LE3, complete genome	16846-16875	9	0.7
NZ_CP042437_12	12.8|6223212|30|NZ_CP042437|CRISPRCasFinder	6223212-6223241	30	MH673674	Thermus phage phiMa, complete genome	6850-6879	9	0.7
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	MH853788	Acinetobacter phage vB_KpnM_IME512, complete genome	44072-44101	9	0.7
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	MK448711	Streptococcus phage Javan235, complete genome	20176-20205	9	0.7
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	MK448893	Streptococcus phage Javan270, complete genome	1289-1318	9	0.7
NZ_CP042437_12	12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223744-6223773	30	AP014858	Vibrio phage RYC DNA, complete sequence	58702-58731	9	0.7
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	NC_023571	Oenococcus phage phiS11, complete genome	42262-42291	9	0.7
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	NC_023559	Oenococcus phage phi9805, complete genome	40342-40371	9	0.7
NZ_CP042437_12	12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6223896-6223925	30	NC_023560	Oenococcus phage phiS13, complete genome	39740-39769	9	0.7
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	MH853788	Acinetobacter phage vB_KpnM_IME512, complete genome	44072-44101	9	0.7
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	MK448711	Streptococcus phage Javan235, complete genome	20176-20205	9	0.7
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	MK448893	Streptococcus phage Javan270, complete genome	1289-1318	9	0.7
NZ_CP042437_12	12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224427-6224456	30	AP014858	Vibrio phage RYC DNA, complete sequence	58702-58731	9	0.7
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	NZ_CP013982	Staphylococcus equorum strain KM1031 plasmid unnamed2, complete sequence	21621-21650	9	0.7
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	NZ_CP013982	Staphylococcus equorum strain KM1031 plasmid unnamed2, complete sequence	46785-46814	9	0.7
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	NZ_CP013717	Staphylococcus equorum strain C2014 plasmid pC2014-3, complete sequence	11036-11065	9	0.7
NZ_CP042437_12	12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225339-6225368	30	NC_015708	Pseudoalteromonas sp. SANK 73390 plasmid pTML1 carrying thiomarinol biosynthesis cluster	2620-2649	9	0.7
NZ_CP042437_12	12.44|6225947|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6225947-6225976	30	MF042360	Pseudomonas phage Phabio, complete genome	32197-32226	9	0.7
NZ_CP042437_12	12.55|6226782|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6226782-6226811	30	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	1666931-1666960	9	0.7
NZ_CP042437_12	12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227160-6227189	30	KT151955	Brevibacillus phage Jenst, complete genome	41027-41056	9	0.7
NZ_CP042437_12	12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227160-6227189	30	KT151957	Brevibacillus phage SecTim467, complete genome	41027-41056	9	0.7
NZ_CP042437_12	12.68|6227767|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6227767-6227796	30	NZ_CP024200	Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence	159519-159548	9	0.7
NZ_CP042437_12	12.75|6228299|30|NZ_CP042437|CRISPRCasFinder	6228299-6228328	30	HM144387	Bacillus phage W.Ph., complete genome	87240-87269	9	0.7
NZ_CP042437_12	12.95|6229819|30|NZ_CP042437|CRISPRCasFinder	6229819-6229848	30	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1116495-1116524	9	0.7
NZ_CP042437_12	12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230273-6230302	30	EU545650	Acidianus filamentous virus 9, complete genome	5003-5032	9	0.7
NZ_CP042437_12	12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6230653-6230682	30	EU545650	Acidianus filamentous virus 9, complete genome	5003-5032	9	0.7
NZ_CP042437_13	13.1|6453774|34|NZ_CP042437|CRISPRCasFinder	6453774-6453807	34	MK552327	Pseudomonas phage Psa21, complete genome	86811-86844	9	0.735
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	MF974397	Leptospira phage LE4, complete genome	16252-16281	10	0.667
NZ_CP042437_12	12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR	6224959-6224988	30	AP013402	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S38-C27	31346-31375	10	0.667
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	NZ_CP006906	Clostridium baratii str. Sullivan plasmid pCBJ, complete sequence	176658-176687	12	0.6
NZ_CP042437_12	12.5|6222985|30|NZ_CP042437|CRISPRCasFinder	6222985-6223014	30	MK911750	Streptococcus phage P738, complete genome	23712-23741	13	0.567

1. spacer 12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MH617085 (Microviridae sp. isolate ctjj553, complete genome) position: , mismatch: 3, identity: 0.897

ataagcggaggaagctacgaagactgggt	CRISPR spacer
ctaagcggaggaagctacgacgactggct	Protospacer
 ******************* ****** *

2. spacer 12.27|6224655|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP044465 (Acinetobacter schindleri strain HZE23-1 plasmid pHZE23-1-2, complete sequence) position: , mismatch: 4, identity: 0.867

atatc-ccaaaagcaggtaaagcttccttgc	CRISPR spacer
-tatcaacaaaagcagggatagcttccttgc	Protospacer
 ****  ********** * ***********

3. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to HG531805 (Clostridium phage CDMH1 complete genome) position: , mismatch: 4, identity: 0.867

tctgaatc---tgaaaataagataaaagaatta	CRISPR spacer
---gaatcaaatgaaaataagttaaaagaatta	Protospacer
   *****   ********** ***********

4. spacer 12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MH617412 (Microviridae sp. isolate cteb899, complete genome) position: , mismatch: 4, identity: 0.862

ataagcggaggaagctacgaagactgggt	CRISPR spacer
gtaagcggaggaagttacgacgactggct	Protospacer
.*************.***** ****** *

5. spacer 12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MH617030 (Microviridae sp. isolate ctbd804, complete genome) position: , mismatch: 4, identity: 0.862

ataagcggaggaagctacgaagactgggt	CRISPR spacer
gtaagcggaggaagctacgacgattggtt	Protospacer
.******************* **.*** *

6. spacer 12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK012486 (Microviridae sp. isolate ctbj6, complete genome) position: , mismatch: 4, identity: 0.862

ataagcggaggaagctacgaagactgggt	CRISPR spacer
gtaagcggaggaagctacaaggactggat	Protospacer
.*****************.*.******.*

7. spacer 12.107|6230729|29|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MH617339 (Microviridae sp. isolate ctjd540, complete genome) position: , mismatch: 4, identity: 0.862

ataagcggaggaagctacgaagactgggt	CRISPR spacer
gtaagcggaggaagttacgacgactggtt	Protospacer
.*************.***** ****** *

8. spacer 2.1|1755532|30|NZ_CP042437|CRISPRCasFinder matches to HQ634193 (Cyanophage P-RSM6 genomic sequence) position: , mismatch: 5, identity: 0.833

attgttaaagtttatattaaagttgggatt	CRISPR spacer
attattaaagtttatagtaaagttaccatt	Protospacer
***.************ *******.  ***

9. spacer 8.2|3121193|28|NZ_CP042437|CRISPRCasFinder matches to NZ_AP017565 (Pseudanabaena sp. ABRG5-3 plasmid ABRG53e, complete sequence) position: , mismatch: 5, identity: 0.821

ggccgaacttgccatcgcaaataacgag	CRISPR spacer
agacaaacttgccatcgcaatttacgag	Protospacer
.* *.*************** * *****

10. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to NZ_LR134429 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 20) position: , mismatch: 5, identity: 0.815

catgatttttgttgtacttatggctaa	CRISPR spacer
gaagatttttgttttacttatggcgat	Protospacer
 * ********** ********** * 

11. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP044540 (Borrelia sp. CA690 plasmid lp17, complete sequence) position: , mismatch: 5, identity: 0.833

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
ccttccccttttttttaaaaaaaggggaag	Protospacer
 *. *******************.***** 

12. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP044540 (Borrelia sp. CA690 plasmid lp17, complete sequence) position: , mismatch: 5, identity: 0.833

accaccccttttttttaaaaaaaagggaac-	CRISPR spacer
-cttccccttttttttaaaaaaaggggaaga	Protospacer
 *. *******************.*****  

13. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP013648 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C99-MedDCM-OCT-S33-C45, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 5, identity: 0.833

taaagaagatgatgtaaattttgc-cgatcg	CRISPR spacer
taaagaagctgatgtaaattctgcaccatt-	Protospacer
******** ***********.*** * **. 

14. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK250028 (Prevotella phage Lak-B9, complete genome) position: , mismatch: 5, identity: 0.833

--tctgaatctgaaaataagataaaagaatta	CRISPR spacer
cgtcttaa--agaaaaaaagataaaagaatta	Protospacer
  *** **   ***** ***************

15. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK250025 (Prevotella phage Lak-B6, complete genome) position: , mismatch: 5, identity: 0.833

--tctgaatctgaaaataagataaaagaatta	CRISPR spacer
cgtcttaa--agaaaaaaagataaaagaatta	Protospacer
  *** **   ***** ***************

16. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK250022 (Prevotella phage Lak-B3, complete genome) position: , mismatch: 5, identity: 0.833

--tctgaatctgaaaataagataaaagaatta	CRISPR spacer
cgtcttaa--agaaaaaaagataaaagaatta	Protospacer
  *** **   ***** ***************

17. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK250020 (Prevotella phage Lak-B1, complete genome) position: , mismatch: 5, identity: 0.833

--tctgaatctgaaaataagataaaagaatta	CRISPR spacer
cgtcttaa--agaaaaaaagataaaagaatta	Protospacer
  *** **   ***** ***************

18. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_024989 (Clostridium botulinum plasmid pMI06-01 DNA, complete genome, strain: Miyagi2006-01) position: , mismatch: 5, identity: 0.833

tctgaat-ctgaaaataagataaaagaatta	CRISPR spacer
-ctaaataaagaaaataagattaaagaatta	Protospacer
 **.***   *********** *********

19. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_025002 (Clostridium botulinum plasmid pTO08 DNA, complete genome, strain: Tochigi2008) position: , mismatch: 5, identity: 0.833

tctgaat-ctgaaaataagataaaagaatta	CRISPR spacer
-ctaaataaagaaaataagattaaagaatta	Protospacer
 **.***   *********** *********

20. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to MH616914 (Inoviridae sp. isolate ctfh53, complete genome) position: , mismatch: 5, identity: 0.833

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
agggagccaacgaccagcaggaacaacaag	Protospacer
*.* ******* ************* *** 

21. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to MH319754 (Marine virus AG-345-L05 Ga0172272_11 genomic sequence) position: , mismatch: 5, identity: 0.833

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
aataaatcaaccaccagcagcaacaccaac	Protospacer
**  *..************* *********

22. spacer 2.1|1755532|30|NZ_CP042437|CRISPRCasFinder matches to MN276049 (Acinetobacter phage BS46, complete genome) position: , mismatch: 6, identity: 0.8

attgttaaagtttatattaaagttgggatt	CRISPR spacer
cctgttaaagttgatattaaagttgaaaat	Protospacer
 .********** ************..* *

23. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to KX501134 (Phage DP-2017a isolate CA39E hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds) position: , mismatch: 6, identity: 0.778

catgatttttgttgtacttatggctaa	CRISPR spacer
actgatttttgttgtactaatggtaca	Protospacer
  **************** ****.  *

24. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to KX501136 (Phage DP-2017a isolate CA40B hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds) position: , mismatch: 6, identity: 0.778

catgatttttgttgtacttatggctaa	CRISPR spacer
actgatttttgttgtactaatggtaca	Protospacer
  **************** ****.  *

25. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to KX501135 (Phage DP-2017a isolate CA40A hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds) position: , mismatch: 6, identity: 0.778

catgatttttgttgtacttatggctaa	CRISPR spacer
actgatttttgttgtactaatggtaca	Protospacer
  **************** ****.  *

26. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to KX501137 (Phage DP-2017a isolate CA40C hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds) position: , mismatch: 6, identity: 0.778

catgatttttgttgtacttatggctaa	CRISPR spacer
actgatttttgttgtactaatggtaca	Protospacer
  **************** ****.  *

27. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to KX501138 (Phage DP-2017a isolate CA40D hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds) position: , mismatch: 6, identity: 0.778

catgatttttgttgtacttatggctaa	CRISPR spacer
actgatttttgttgtactaatggtaca	Protospacer
  **************** ****.  *

28. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to KX501139 (Phage DP-2017a isolate CA40E hypothetical protein, tape measure, hypothetical protein, LysM, D-like protein, hypothetical protein, type IV secretion protein, baseplate, hypothetical protein, hydrolase, hypothetical protein, helicase, primase, type III restriction endonuclease, and exonuclease genes, complete cds) position: , mismatch: 6, identity: 0.778

catgatttttgttgtacttatggctaa	CRISPR spacer
actgatttttgttgtactaatggtaca	Protospacer
  **************** ****.  *

29. spacer 11.2|5590057|27|NZ_CP042437|CRISPRCasFinder matches to NC_021794 (Cellulophaga phage phi18:3, complete genome) position: , mismatch: 6, identity: 0.778

catgatttttgttgtacttatggctaa	CRISPR spacer
catgttttttgttgtacttatttattt	Protospacer
**** ****************   *  

30. spacer 12.3|6222833|30|NZ_CP042437|CRISPRCasFinder matches to MN379631 (Chicken microvirus mg4_164, complete genome) position: , mismatch: 6, identity: 0.8

atggc-agtttcacaaacgtgccggtttcga	CRISPR spacer
-tgactcgtttcacaaacgcgcctgtttcgg	Protospacer
 **.*  ************.*** ******.

31. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP044540 (Borrelia sp. CA690 plasmid lp17, complete sequence) position: , mismatch: 6, identity: 0.8

accaccccttttttttaaaaaaaagggaac--	CRISPR spacer
--ttccccttttttttaaaaaaaggggaagaa	Protospacer
  . *******************.*****   

32. spacer 12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP038863 (Campylobacter jejuni strain SCJK2 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.8

ttttacttttgaaataagcatctacatatt	CRISPR spacer
aatcacttttgaaagaagcatctatatata	Protospacer
  *.********** *********.**** 

33. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP013122 (Fusobacterium nucleatum subsp. polymorphum strain ChDC F306 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt-----	CRISPR spacer
agggctttaaaataaaaaag-----caagttgata	Protospacer
**** ***************     *****     

34. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP013877 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C117A-MedDCM-OCT-S27-C30, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aggtgtttagaataaaaaagcctttaaagc	Protospacer
*** *****.*************.  ***.

35. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to CP033552 (Acinetobacter nosocomialis strain 2014S01-097 plasmid p2014S01-097-2, complete sequence) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt--	CRISPR spacer
ttgggtctaaaataaaaaagc--cacaaatta	Protospacer
  ****.**************  *****.*  

36. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP013511 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G21, isolate: uvMED-CGR-C117A-MedDCM-OCT-S32-C49) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aggtgtttagaataaaaaagcctttaaagc	Protospacer
*** *****.*************.  ***.

37. spacer 12.16|6223820|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP049159 (Caballeronia sp. SBC1 plasmid pSBC1_3, complete sequence) position: , mismatch: 6, identity: 0.8

tttgcttttttatgatcaacctcgccgcct	CRISPR spacer
gtcgcttttgtatgatcaacctcgcaatct	Protospacer
 *.****** *************** ..**

38. spacer 12.16|6223820|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP049319 (Caballeronia sp. SBC2 plasmid pSBC2-3, complete sequence) position: , mismatch: 6, identity: 0.8

tttgcttttttatgatcaacctcgccgcct	CRISPR spacer
gtcgcttttgtatgatcaacctcgcaatct	Protospacer
 *.****** *************** ..**

39. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP032629 (Lactococcus sp. 1JSPR-7 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.8

taaagaagatgatgtaaattttg-ccgatcg	CRISPR spacer
taaagaagattatgcaaattttgaactacc-	Protospacer
********** ***.********  * *.* 

40. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_014502 (Gloeothece verrucosa PCC 7822 plasmid Cy782203, complete sequence) position: , mismatch: 6, identity: 0.8

taaagaagatgatgtaaattt---tgccgatcg	CRISPR spacer
taaaaaagatgatgtaaatttatgtccgga---	Protospacer
****.****************   * * **   

41. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_014502 (Gloeothece verrucosa PCC 7822 plasmid Cy782203, complete sequence) position: , mismatch: 6, identity: 0.8

taaagaagatgatgtaaattt---tgccgatcg	CRISPR spacer
taaaaaagatgatgtaaatttatgtccgga---	Protospacer
****.****************   * * **   

42. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP013122 (Fusobacterium nucleatum subsp. polymorphum strain ChDC F306 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt-----	CRISPR spacer
agggctttaaaataaaaaag-----caagttgata	Protospacer
**** ***************     *****     

43. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP013877 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C117A-MedDCM-OCT-S27-C30, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aggtgtttagaataaaaaagcctttaaagc	Protospacer
*** *****.*************.  ***.

44. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to CP033552 (Acinetobacter nosocomialis strain 2014S01-097 plasmid p2014S01-097-2, complete sequence) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt--	CRISPR spacer
ttgggtctaaaataaaaaagc--cacaaatta	Protospacer
  ****.**************  *****.*  

45. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP013511 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G21, isolate: uvMED-CGR-C117A-MedDCM-OCT-S32-C49) position: , mismatch: 6, identity: 0.8

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aggtgtttagaataaaaaagcctttaaagc	Protospacer
*** *****.*************.  ***.

46. spacer 12.32|6225035|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to HM144385 (Brochothrix phage NF5, complete genome) position: , mismatch: 6, identity: 0.8

ttaacaaacgaataaccgcatccgtaccat-	CRISPR spacer
attacaaacgaataacagcatccgt-tgatg	Protospacer
 * ************* ******** . ** 

47. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_020394 (Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-233, complete sequence) position: , mismatch: 6, identity: 0.8

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
ttagaatacgaaaataagataaaagagata	Protospacer
*. **** .*****************. **

48. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to CP020755 (Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-16, complete sequence) position: , mismatch: 6, identity: 0.8

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
ttagaatacgaaaataagataaaagagata	Protospacer
*. **** .*****************. **

49. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP021062 (Bacillus thuringiensis strain ATCC 10792 plasmid poh1, complete sequence) position: , mismatch: 6, identity: 0.8

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
ttagaatacgaaaataagataaaagagata	Protospacer
*. **** .*****************. **

50. spacer 12.41|6225719|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MN693703 (Marine virus AFVG_250M594, complete genome) position: , mismatch: 6, identity: 0.8

tttgatttttgtttgaagtttttcatattc	CRISPR spacer
gttgattttggtttgaagttttccatagca	Protospacer
 ******** ************.**** . 

51. spacer 12.52|6226554|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KJ019071 (Synechococcus phage ACG-2014g isolate Syn7803US105, complete genome) position: , mismatch: 6, identity: 0.8

cactatcgaagagtttaggggtatttacaa	CRISPR spacer
cactaccgaagagtttatgggtagtaagat	Protospacer
*****.*********** ***** * * * 

52. spacer 12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP018213 (Lactobacillus plantarum strain BLS41 plasmid pLPBLS41_4, complete sequence) position: , mismatch: 6, identity: 0.8

-ttggcacaatgctaagattgatgatataat	CRISPR spacer
attcgt-caatgccaagattgctgatataaa	Protospacer
 ** *. ******.******* ******** 

53. spacer 12.62|6227311|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_015583 (Novosphingobium sp. PP1Y plasmid Mpl, complete sequence) position: , mismatch: 6, identity: 0.8

cgcggttcagatcgcggcaaacatcttcta	CRISPR spacer
cgcgggtcagattgcggcaaacagtcccta	Protospacer
***** ******.********** ...***

54. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK893987 (Staphylococcus phage PMBT8, complete genome) position: , mismatch: 6, identity: 0.8

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
attatttaattcacaaaaatcataaacaac	Protospacer
*. * ********** ****** ******.

55. spacer 12.93|6229667|30|NZ_CP042437|CRISPRCasFinder matches to NZ_AP022607 (Mycobacterium branderi strain JCM 12687 plasmid pJCM12687) position: , mismatch: 6, identity: 0.8

catgg-ccgcttcttttgccctacgggctac	CRISPR spacer
-acgatccgcttcttttgccatccgggctgc	Protospacer
 *.*. ************** * ******.*

56. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 6, identity: 0.8

gaggctaaaatacaagtaaagacagcaaaa-	CRISPR spacer
gaggctaaaataaatgtaaagac-gcacgtc	Protospacer
************ * ******** *** .  

57. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 6, identity: 0.8

gaggctaaaatacaagtaaagacagcaaaa-	CRISPR spacer
gaggctaaaataaatgtaaagac-gcacgtc	Protospacer
************ * ******** *** .  

58. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP007513 (Bacillus bombysepticus plasmid pBb, complete genome) position: , mismatch: 6, identity: 0.8

gaggctaaaatacaagtaaagacagcaaaa-	CRISPR spacer
gaggctaaaataaatgtaaagac-gcacgtc	Protospacer
************ * ******** *** .  

59. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP050184 (Bacillus thuringiensis strain HER1410 plasmid pLUSID1, complete sequence) position: , mismatch: 6, identity: 0.8

gaggctaaaatacaagtaaagacagcaaaa-	CRISPR spacer
gaggctaaaataaatgtaaagac-gcacgtc	Protospacer
************ * ******** *** .  

60. spacer 2.1|1755532|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP032095 (Vibrio alfacsensis strain CAIM 1831 plasmid pVa1, complete sequence) position: , mismatch: 7, identity: 0.767

attgttaaagtttatattaaagttgggatt--	CRISPR spacer
attgttaaactttatagtaaagt--aaatcaa	Protospacer
********* ****** ******  ..**.  

61. spacer 2.1|1755532|30|NZ_CP042437|CRISPRCasFinder matches to NZ_AP018256 (Calothrix sp. NIES-4071 plasmid plasmid1 DNA, complete genome) position: , mismatch: 7, identity: 0.767

attgttaaagtttatattaaagttgggatt	CRISPR spacer
attattaaagtttatatttaagtacttact	Protospacer
***.************** ****    *.*

62. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP020436 (Bacillus sp. FDAARGOS_235 plasmid 2, complete sequence) position: , mismatch: 7, identity: 0.767

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
aatcaaccttttttttgaaaaaaagggaat	Protospacer
* .   **********.************.

63. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP014289 (Bacillus thuringiensis strain Bt185 plasmid pBT1850046, complete sequence) position: , mismatch: 7, identity: 0.767

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
gctttccctttttttttagaaaaagggaaa	Protospacer
.*. .*********** *.********** 

64. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP047434 (Spiroplasma citri strain BLH-13 plasmid pSciBLH13-6) position: , mismatch: 7, identity: 0.767

accaccccttttttttaaaaaaaagggaac--	CRISPR spacer
--catccctcttttttaaaaaaaagaggaacg	Protospacer
  **.****.***************.*.*   

65. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP047434 (Spiroplasma citri strain BLH-13 plasmid pSciBLH13-6) position: , mismatch: 7, identity: 0.767

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
gtcatccctcttttttaaaaaaaagaggaa	Protospacer
..**.****.***************.*.* 

66. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP033050 (Virgibacillus halodenitrificans strain Bac324 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
aacgaaacttttttataaaaaaaagagaac	Protospacer
* *.   ******* **********.****

67. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP034710 (Salmonella enterica subsp. enterica serovar Karamoja strain RSE21 plasmid pRSE21, complete sequence) position: , mismatch: 7, identity: 0.767

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
accaccacttttttttataaaaatatccac	Protospacer
****** ********** ***** .   **

68. spacer 12.10|6223364|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_012473 (Bacillus cereus 03BB102 plasmid p03BB102_179, complete sequence) position: , mismatch: 7, identity: 0.767

cggcaaggtgtttagaaccttccg-caggca	CRISPR spacer
tcgcaaggtgtttagcaccttccatcatac-	Protospacer
. ************* *******. ** .* 

69. spacer 12.10|6223364|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP009317 (Bacillus cereus 03BB102 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cggcaaggtgtttagaaccttccg-caggca	CRISPR spacer
tcgcaaggtgtttagcaccttccatcatac-	Protospacer
. ************* *******. ** .* 

70. spacer 12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP045419 (Pseudoalteromonas sp. THAF3 plasmid pTHAF3_a, complete sequence) position: , mismatch: 7, identity: 0.767

tgacggcaagctgctgcccgg---atgggatat	CRISPR spacer
tgacggcaagctggtgcccggcgcactggc---	Protospacer
************* *******   *. **    

71. spacer 12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to HM152765 (Mycobacterium phage Island3, complete genome) position: , mismatch: 7, identity: 0.767

tgacggcaagctgctgcccggatgggatat	CRISPR spacer
cgagatcatgctgctgcccggatgggagaa	Protospacer
.** . ** ****************** * 

72. spacer 12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_011291 (Mycobacterium phage Brujita, complete genome) position: , mismatch: 7, identity: 0.767

tgacggcaagctgctgcccggatgggatat	CRISPR spacer
cgagatcatgctgctgcccggatgggagaa	Protospacer
.** . ** ****************** * 

73. spacer 12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to CP016195 (Bacillus thuringiensis serovar coreanensis strain ST7 plasmid pST7-1, complete sequence) position: , mismatch: 7, identity: 0.767

ttttacttttgaaataagcatctacatatt	CRISPR spacer
catgaacttttaaataagaatctacatatt	Protospacer
. * * .*** ******* ***********

74. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT962247 (Cellulophaga phage phi17:2_18, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

75. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT962246 (Cellulophaga phage phi4:1_18, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

76. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT962245 (Cellulophaga phage phi4:1_13, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

77. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KC821632 (Cellulophaga phage phi4:1, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

78. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_021798 (Cellulophaga phage phi17:2, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

79. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT962247 (Cellulophaga phage phi17:2_18, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

80. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT962246 (Cellulophaga phage phi4:1_18, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

81. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT962245 (Cellulophaga phage phi4:1_13, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

82. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KC821632 (Cellulophaga phage phi4:1, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

83. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_021798 (Cellulophaga phage phi17:2, complete genome) position: , mismatch: 7, identity: 0.767

aggggtt-----taaaataaaaaagcctcacaagt	CRISPR spacer
-----ttacccgtaaaataaaaaagcctcccaaat	Protospacer
     **     ***************** ***.*

84. spacer 12.33|6225111|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP025980 (Escherichia marmotae strain HT073016 plasmid pEM148, complete sequence) position: , mismatch: 7, identity: 0.767

tgcatcaggaaaataaacagcatgatttgt	CRISPR spacer
ccgatcaggaaaatcaccagcatgatttcc	Protospacer
.  *********** * *********** .

85. spacer 12.33|6225111|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to LC425522 (Uncultured phage DNA, contig: NODE620) position: , mismatch: 7, identity: 0.767

tgcatcaggaaaataaacagcatgatttgt	CRISPR spacer
ttcgtcaggaaaataaacaccctgattaag	Protospacer
* *.*************** * ***** . 

86. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_048665 (Clostridium phage phiCDHM14, complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
gaagaatttgaaactaagataaaagaaatg	Protospacer
   ****.***** ************* *.

87. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to HG796225 (Clostridium phage phiCDHM13 complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
gaagaatttgaaactaagataaaagaaatg	Protospacer
   ****.***** ************* *.

88. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to HG798901 (Clostridium phage phiCDHM11 complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
gaagaatttgaaactaagataaaagaaatg	Protospacer
   ****.***** ************* *.

89. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK473382 (Clostridium phage JD032, complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
gaagaatttgaaactaagataaaagaaatg	Protospacer
   ****.***** ************* *.

90. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MN693097 (Marine virus AFVG_25M78, complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
aaagaattagaaaataagataaaagaaaga	Protospacer
   ****. ******************  *

91. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MH552526 (Siphoviridae sp. isolate ctfj46, complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
aaggaaaaagataataagataaaagaatta	Protospacer
   ***   ** ******************

92. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_002669 (Lactococcus prophage bIL310, complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
cttgaatctgacaataaaataaaagcagtt	Protospacer
..********* *****.******* * * 

93. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK774614 (Aeromonas phage CF8, complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
atttatcccgaaaataagagaaaagaatta	Protospacer
 .* * .*.********** **********

94. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AF323671 (Bacteriophage bIL310, complete genome) position: , mismatch: 7, identity: 0.767

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
cttgaatctgacaataaaataaaagcagtt	Protospacer
..********* *****.******* * * 

95. spacer 12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_023917 (Clostridium perfringens plasmid pCP-OS1 DNA, complete sequence, strain: OS1) position: , mismatch: 7, identity: 0.767

tgtttttgttacataaattgtataccctgc	CRISPR spacer
caaatcagttacataaattgtatcccctgc	Protospacer
..  *. **************** ******

96. spacer 12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_023918 (Clostridium perfringens plasmid pCP-TS1 DNA, complete sequence, strain: TS1) position: , mismatch: 7, identity: 0.767

tgtttttgttacataaattgtataccctgc	CRISPR spacer
caaatcagttacataaattgtatcccctgc	Protospacer
..  *. **************** ******

97. spacer 12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_011255 (Borrelia recurrentis A1 plasmid pl35, complete sequence) position: , mismatch: 7, identity: 0.767

tgtttttgttacataaattgtataccctgc	CRISPR spacer
gatttttgttaaattaattgtatactatgt	Protospacer
 .********* ** **********. **.

98. spacer 12.51|6226478|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP019737 (Lactobacillus brevis strain TMW 1.2108 plasmid pl12108-3, complete sequence) position: , mismatch: 7, identity: 0.767

ttttttgcgttttcatagcgattgtatctg	CRISPR spacer
acttccgcgtcttcatagcgattgtattta	Protospacer
 .**..****.****************.*.

99. spacer 12.51|6226478|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP019746 (Lactobacillus brevis strain TMW 1.2111 plasmid pl12111-3, complete sequence) position: , mismatch: 7, identity: 0.767

ttttttgcgttttcatagcgattgtatctg	CRISPR spacer
acttccgcgtcttcatagcgattgtattta	Protospacer
 .**..****.****************.*.

100. spacer 12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_049968 (Bacillus phage DK2, complete genome) position: , mismatch: 7, identity: 0.767

-----ttggcacaatgctaagattgatgatataat	CRISPR spacer
agctatt-----aatgctaaaattgatgatatatt	Protospacer
     **     ********.************ *

101. spacer 12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK284528 (Bacillus phage DK3, complete genome) position: , mismatch: 7, identity: 0.767

-----ttggcacaatgctaagattgatgatataat	CRISPR spacer
agctatt-----aatgctaaaattgatgatatatt	Protospacer
     **     ********.************ *

102. spacer 12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK284526 (Bacillus phage DK1, complete genome) position: , mismatch: 7, identity: 0.767

-----ttggcacaatgctaagattgatgatataat	CRISPR spacer
agctatt-----aatgctaaaattgatgatatatt	Protospacer
     **     ********.************ *

103. spacer 12.63|6227387|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK552327 (Pseudomonas phage Psa21, complete genome) position: , mismatch: 7, identity: 0.767

atagccatgatatttaataggggttttaaa	CRISPR spacer
caaaacatgatttttaataagggttttata	Protospacer
  *. ****** *******.******** *

104. spacer 12.71|6227995|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP045607 (Bacillus cereus strain SB1 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.767

aaatggtggctgataaacagctacaaaacc	CRISPR spacer
acatggtccctgataaacagctacaggaat	Protospacer
* *****  ****************..* .

105. spacer 12.71|6227995|30|NZ_CP042437|CRISPRCasFinder matches to LR134127 (Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 7) position: , mismatch: 7, identity: 0.767

aaatggtggctgataaacagctacaaaacc	CRISPR spacer
aaatcgtggctgataaacagataggccagc	Protospacer
**** *************** ** .  * *

106. spacer 12.71|6227995|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 7, identity: 0.767

aaatggtggctgataaacagctacaaaacc	CRISPR spacer
acatggtccctgataaacagctacaggaat	Protospacer
* *****  ****************..* .

107. spacer 12.71|6227995|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP014283 (Bacillus thuringiensis strain Bt185 plasmid pBT1850636, complete sequence) position: , mismatch: 7, identity: 0.767

aaatggtggctgataaacagctacaaaacc	CRISPR spacer
acatggtccctgataaacagctacaggaat	Protospacer
* *****  ****************..* .

108. spacer 12.71|6227995|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 7, identity: 0.767

aaatggtggctgataaacagctacaaaacc	CRISPR spacer
acatggtccctgataaacagctacaggaat	Protospacer
* *****  ****************..* .

109. spacer 12.71|6227995|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP032614 (Bacillus thuringiensis strain QZL38 plasmid p.1, complete sequence) position: , mismatch: 7, identity: 0.767

aaatggtggctgataaacagctacaaaacc	CRISPR spacer
acatggtccctgataaacagctacaggaat	Protospacer
* *****  ****************..* .

110. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP048619 (Legionella pneumophila strain ERS1305867 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
tttccagaatttaataactcaacagctaaa	Protospacer
. *.* .*****.*.***************

111. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP041669 (Legionella israelensis strain L18-01051 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
acaaattaatccacataaaacaatcatcag	Protospacer
**********.******** ***  *. * 

112. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448514 (Streptococcus satellite phage Javan480, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

113. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448347 (Streptococcus satellite phage Javan171, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

114. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448508 (Streptococcus satellite phage Javan466, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

115. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448346 (Streptococcus satellite phage Javan168, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

116. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448344 (Streptococcus satellite phage Javan165, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

117. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448339 (Streptococcus satellite phage Javan154, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

118. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448329 (Streptococcus satellite phage Javan134, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

119. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448325 (Streptococcus satellite phage Javan125, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

120. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448326 (Streptococcus satellite phage Javan127, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

121. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to MK448335 (Streptococcus satellite phage Javan148, complete genome) position: , mismatch: 7, identity: 0.767

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
taaaattacttcaaataaatcaaaacaagt	Protospacer
  ****** **** ***********  *.*

122. spacer 12.77|6228451|30|NZ_CP042437|CRISPRCasFinder matches to MH572451 (Microviridae sp. isolate SD_MC_7, complete genome) position: , mismatch: 7, identity: 0.767

ctgatggtgtatttagcctggaaaagcttg	CRISPR spacer
cgatgggtgtatttagcctggcaaagaatg	Protospacer
* .  **************** ****  **

123. spacer 12.78|6228527|30|NZ_CP042437|CRISPRCasFinder matches to MN694130 (Marine virus AFVG_250M413, complete genome) position: , mismatch: 7, identity: 0.767

actttggctcgggcttctttccaaatatct	CRISPR spacer
ccccaggatcgggcttcttttcaaatatcc	Protospacer
 *.. ** ************.********.

124. spacer 12.87|6229211|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP019972 (Enterococcus faecium isolate 2014-VREF-114 plasmid p114-2 sequence) position: , mismatch: 7, identity: 0.767

taggagcattcaaatcaacagcaaacagca	CRISPR spacer
cacgagcattcaaataaacatcaaacaatc	Protospacer
.* ************ **** ******.. 

125. spacer 12.91|6229515|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP021406 (Celeribacter manganoxidans strain DY25 plasmid pDY25-B, complete sequence) position: , mismatch: 7, identity: 0.767

-cgcaatcggctctatctttcccggtattgg	CRISPR spacer
gtgcgg-cggctctatcctttccggtattgt	Protospacer
 .**.. **********.**.********* 

126. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP021449 (Ralstonia solanacearum strain SEPPX05 plasmid pSEPPX05, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

127. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to CP023013 (Ralstonia solanacearum strain T110 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

128. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP049790 (Ralstonia solanacearum strain 202 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

129. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP049794 (Ralstonia solanacearum strain 204 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

130. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP049788 (Ralstonia solanacearum strain B2 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

131. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP021763 (Ralstonia pseudosolanacearum strain RS 476 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

132. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP015116 (Ralstonia solanacearum strain EP1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

133. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP049792 (Ralstonia solanacearum strain 203 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

134. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP016915 (Ralstonia solanacearum strain CQPS-1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

135. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

136. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP015851 (Ralstonia solanacearum strain YC40-M plasmid, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

137. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP022783 (Ralstonia solanacearum strain SL3755 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

138. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP022795 (Ralstonia solanacearum strain SL2330 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

139. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP009763 (Ralstonia solanacearum OE1-1 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

140. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to CP023015 (Ralstonia solanacearum strain T25 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

141. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052085 (Ralstonia solanacearum strain FJAT15353.F8 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

142. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052095 (Ralstonia solanacearum strain FJAT15340.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

143. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

144. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052077 (Ralstonia solanacearum strain FJAT445.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

145. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052087 (Ralstonia solanacearum strain FJAT15353.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

146. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052097 (Ralstonia solanacearum strain FJAT15304.F6 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

147. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052127 (Ralstonia solanacearum strain FJAT1303.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

148. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052079 (Ralstonia solanacearum strain FJAT445.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

149. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052089 (Ralstonia solanacearum strain FJAT15353.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

150. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052093 (Ralstonia solanacearum strain FJAT15340.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

151. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052101 (Ralstonia solanacearum strain FJAT15304.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

152. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052099 (Ralstonia solanacearum strain FJAT15304.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

153. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052125 (Ralstonia solanacearum strain FJAT1452.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

154. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052129 (Ralstonia solanacearum strain FJAT1303.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

155. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052123 (Ralstonia solanacearum strain FJAT1452.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

156. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052131 (Ralstonia solanacearum strain FJAT1303.F8 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

157. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052081 (Ralstonia solanacearum strain FJAT442.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

158. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052083 (Ralstonia solanacearum strain FJAT442.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

159. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052091 (Ralstonia solanacearum strain FJAT15340.F6 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

160. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052111 (Ralstonia solanacearum strain FJAT15244.F50 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

161. spacer 12.92|6229591|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP052113 (Ralstonia solanacearum strain FJAT15244.F1 plasmid Plas1, complete sequence) position: , mismatch: 7, identity: 0.767

tgaacccgcagcccttaacaggtttcctac	CRISPR spacer
ggaaccagcagcccttaacagcttgcttca	Protospacer
 ***** ************** ** *.*  

162. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to JQ182733 (Enterobacterial phage mEp213, complete genome) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
accaatataaccaccagcaggaacaccaaa	Protospacer
*   *  .********************* 

163. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to JQ182730 (Enterobacteria phage mEp237, complete genome) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
accaatataaccaccagcaggaacaccaaa	Protospacer
*   *  .********************* 

164. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to NC_019706 (Enterobacteria phage mEp043 c-1, complete genome) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
accaatataaccaccagcaggaacaccaaa	Protospacer
*   *  .********************* 

165. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to KM389288 (UNVERIFIED: Escherichia phage Phi06_2987 S clone contig00002 genomic sequence) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
accaatataaccaccagcaggaacaccaaa	Protospacer
*   *  .********************* 

166. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to NC_011892 (Methylobacterium nodulans ORS 2060 plasmid pMNOD01, complete sequence) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
taaacgccgaccaccagcaggaacacctgc	Protospacer
 *.  ***.****************** .*

167. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to AP014139 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C47-MedDCM-OCT-S39-C56, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
aatttttgtaccaccagcaggaataccaac	Protospacer
** *  .  **************.******

168. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP028348 (Novosphingobium sp. THN1 plasmid pTHN, complete sequence) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
aggcggccaacaaccagcaggaacgccaga	Protospacer
*.*..****** ************.***. 

169. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to AP014138 (Uncultured Mediterranean phage uvMED isolate uvMED-GF-C47-MedDCM-OCT-S36-C43, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 7, identity: 0.767

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
aacttttgtaccaccagcaggaataccaac	Protospacer
** *  .  **************.******

170. spacer 12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_019542 (Pectobacterium phage PP1, complete genome) position: , mismatch: 7, identity: 0.767

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
gtaccaatgctaatagcaatagctggaacg	Protospacer
**************.*****.**..*.  *

171. spacer 12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KY744566 (Pectobacterium phage POP72, complete genome) position: , mismatch: 7, identity: 0.767

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
gtaccaatgctaatagcaatagctggaacg	Protospacer
**************.*****.**..*.  *

172. spacer 12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_019542 (Pectobacterium phage PP1, complete genome) position: , mismatch: 7, identity: 0.767

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
gtaccaatgctaatagcaatagctggaacg	Protospacer
**************.*****.**..*.  *

173. spacer 12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KY744566 (Pectobacterium phage POP72, complete genome) position: , mismatch: 7, identity: 0.767

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
gtaccaatgctaatagcaatagctggaacg	Protospacer
**************.*****.**..*.  *

174. spacer 2.1|1755532|30|NZ_CP042437|CRISPRCasFinder matches to MG592580 (Vibrio phage 1.210.O._10N.222.52.C2, partial genome) position: , mismatch: 8, identity: 0.733

attgttaaagtttatattaaagttgggatt	CRISPR spacer
gttgttaaagtttatcttaatgttaagcaa	Protospacer
.************** **** ***..*   

175. spacer 7.1|2921874|35|NZ_CP042437|CRISPRCasFinder matches to MG592621 (Vibrio phage 1.255.O._10N.286.45.F1, partial genome) position: , mismatch: 8, identity: 0.771

ttcgcaacacgaaccacatagccaggttcaggaat	CRISPR spacer
tcaacaacacgaaccacatacgcaggttcattagt	Protospacer
*. .****************  ********  *.*

176. spacer 7.1|2921874|35|NZ_CP042437|CRISPRCasFinder matches to MG592609 (Vibrio phage 1.244.A._10N.261.54.C3, partial genome) position: , mismatch: 8, identity: 0.771

ttcgcaacacgaaccacatagccaggttcaggaat	CRISPR spacer
tcaacaacacgaaccacatacgcaggttcattagt	Protospacer
*. .****************  ********  *.*

177. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP020436 (Bacillus sp. FDAARGOS_235 plasmid 2, complete sequence) position: , mismatch: 8, identity: 0.733

accaccccttttttttaaaaaaaagggaac--	CRISPR spacer
--tcaaccttttttttgaaaaaaagggaatat	Protospacer
  .   **********.************.  

178. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NC_022879 (Enterococcus mundtii QU 25 plasmid pQY182, complete sequence) position: , mismatch: 8, identity: 0.733

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
gtgtcttcttttttttaaaaaaaaggaaaa	Protospacer
..  *..*******************.** 

179. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP043834 (Bacillus sp. BS98 plasmid unnamed4) position: , mismatch: 8, identity: 0.733

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
aatcaaccttttttttgaaaaaaaggaaat	Protospacer
* .   **********.*********.**.

180. spacer 12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

tgacggcaagctgctgcccggatgggatat	CRISPR spacer
caacggcaagctgctgcccgggagggccgc	Protospacer
..*******************. *** ...

181. spacer 12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP039641 (Azospirillum sp. TSH100 plasmid p2, complete sequence) position: , mismatch: 8, identity: 0.733

tgacggcaagctgctgcccggatgggatat	CRISPR spacer
tgacggccagctgctgcccggccgacaggc	Protospacer
******* ************* .*. * ..

182. spacer 12.12|6223516|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MT498036 (Gordonia Phage Zitch, complete genome) position: , mismatch: 8, identity: 0.733

tgacggcaagctgctgcccggatgggatat	CRISPR spacer
gggcggcaagctgctgtccgggtgggccga	Protospacer
 *.*************.****.**** .. 

183. spacer 12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_014633 (Ilyobacter polytropus DSM 2926 plasmid pILYOP01, complete sequence) position: , mismatch: 8, identity: 0.733

ttttacttttgaaataagcatctacatatt	CRISPR spacer
ttttatttttcaaataagcatctctgagat	Protospacer
*****.**** ************ .. . *

184. spacer 12.13|6223592|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MT188223 (Acinetobacter phage vB_AbaM_D22, complete genome) position: , mismatch: 8, identity: 0.733

ttttacttttgaaataagcatctacatatt	CRISPR spacer
ttttactcttcaaataagcatctgagcctc	Protospacer
*******.** ************. .. *.

185. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK448705 (Streptococcus phage Javan215, complete genome) position: , mismatch: 8, identity: 0.733

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aatcaaataaaataaaaaagccacacaaat	Protospacer
*.  .  *************** *****.*

186. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to L37090 (Bacteriophage P001 (from Lactococcus lactis) gene, terminal region) position: , mismatch: 8, identity: 0.733

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aaaaatttaaaataaaaaagcataacaaag	Protospacer
*....**************** * ****. 

187. spacer 12.16|6223820|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP034168 (Enterococcus avium strain 352 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

tttgcttttttatgatcaacctcgccgcct	CRISPR spacer
ccagcttttgtatgatcaaccacgcccttt	Protospacer
.. ****** *********** **** ..*

188. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MN694590 (Marine virus AFVG_250M75, complete genome) position: , mismatch: 8, identity: 0.733

taaagaagatgatgtaaattttgccgatcg	CRISPR spacer
atcagaagatgatgtaaattctgctgttac	Protospacer
   *****************.***.* *  

189. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MN694249 (Marine virus AFVG_250M74, complete genome) position: , mismatch: 8, identity: 0.733

taaagaagatgatgtaaattttgccgatcg	CRISPR spacer
atcagaagatgatgtaaattctgctgttac	Protospacer
   *****************.***.* *  

190. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK448705 (Streptococcus phage Javan215, complete genome) position: , mismatch: 8, identity: 0.733

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aatcaaataaaataaaaaagccacacaaat	Protospacer
*.  .  *************** *****.*

191. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to L37090 (Bacteriophage P001 (from Lactococcus lactis) gene, terminal region) position: , mismatch: 8, identity: 0.733

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
aaaaatttaaaataaaaaagcataacaaag	Protospacer
*....**************** * ****. 

192. spacer 12.26|6224579|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MN693750 (Marine virus AFVG_250M298, complete genome) position: , mismatch: 8, identity: 0.733

gctgtttaagatatgtaggtatcctgataa	CRISPR spacer
gagcgagaagatttgtaggtgtcctgataa	Protospacer
*      ***** *******.*********

193. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP049229 (Lactobacillus iners strain C0210C1 plasmid pC0210C1, complete sequence) position: , mismatch: 8, identity: 0.733

ccacgtagatatatataaagatttttacct	CRISPR spacer
aaaggtcgatatatataaagattttgaaaa	Protospacer
  * ** ****************** *   

194. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP049227 (Lactobacillus iners strain C0011D1 plasmid pC0011D1, complete sequence) position: , mismatch: 8, identity: 0.733

ccacgtagatatatataaagatttttacct	CRISPR spacer
aaaggtcgatatatataaagattttgaaaa	Protospacer
  * ** ****************** *   

195. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to CP002030 (Campylobacter jejuni subsp. jejuni ICDCCJ07001 plasmid pTet, complete sequence) position: , mismatch: 8, identity: 0.733

ccacgtagatatatataaagatttttacct	CRISPR spacer
ttatatagttatatataaaaatttttacaa	Protospacer
..*..*** **********.********  

196. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP025619 (Acinetobacter schindleri strain SGAir0122 plasmid pSGAir0122, complete sequence) position: , mismatch: 8, identity: 0.733

ccacgtagatatatataaagatttttacct	CRISPR spacer
ttacaatgatatatataaaaatttttactc	Protospacer
..**.  ************.********..

197. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP013709 (Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence) position: , mismatch: 8, identity: 0.733

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
ttaataaaagaaaataaaataaaagaatta	Protospacer
*. . *   ********.************

198. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP013844 (Clostridium botulinum strain A634 plasmid pRSJ19_2, complete sequence) position: , mismatch: 8, identity: 0.733

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
ttaataaaagaaaataaaataaaagaatta	Protospacer
*. . *   ********.************

199. spacer 12.34|6225187|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_009700 (Clostridium botulinum F str. Langeland plasmid pCLI, complete sequence) position: , mismatch: 8, identity: 0.733

tctgaatctgaaaataagataaaagaatta	CRISPR spacer
ttaaataaagaaaataaaataaaagaatta	Protospacer
*. .*    ********.************

200. spacer 12.41|6225719|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_LR214999 (Mycoplasma conjunctivae strain NCTC10147 plasmid 3) position: , mismatch: 8, identity: 0.733

tttgatttttgtttgaagtttttcatattc	CRISPR spacer
aattgcttttgtttgacctttttcatattg	Protospacer
  * ..**********  *********** 

201. spacer 12.41|6225719|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to LR214965 (Mycoplasma fermentans strain NCTC10117 genome assembly, plasmid: 11) position: , mismatch: 8, identity: 0.733

tttgatttttgtttgaagtttttcatattc	CRISPR spacer
aattgcttttgtttgacctttttcatattg	Protospacer
  * ..**********  *********** 

202. spacer 12.47|6226175|29|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP049297 (Bacillus megaterium strain S188 plasmid pS188, complete sequence) position: , mismatch: 8, identity: 0.724

actaaatgacatttctatgacaattcaac	CRISPR spacer
catgaatgacatttctatgaaaattattg	Protospacer
  *.**************** ****    

203. spacer 12.55|6226782|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP033220 (Parasedimentitalea marina strain W43 plasmid pW43A, complete sequence) position: , mismatch: 8, identity: 0.733

ggtacccagtacggccaccagggcattatt	CRISPR spacer
cacacccagaacggccaccagggcgaaaat	Protospacer
 ..****** **************.  * *

204. spacer 12.55|6226782|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP033220 (Parasedimentitalea marina strain W43 plasmid pW43A, complete sequence) position: , mismatch: 8, identity: 0.733

ggtacccagtacggccaccagggcattatt	CRISPR spacer
cacacccagaacggccaccagggcgaaaat	Protospacer
 ..****** **************.  * *

205. spacer 12.68|6227767|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP022999 (Rhizobium sp. 11515TR strain 10195 plasmid p11515TR-A, complete sequence) position: , mismatch: 8, identity: 0.733

gcgccaatgataatggcaatggcaaggaga	CRISPR spacer
gcggcaatggtaatggcaatggcggcggtc	Protospacer
*** *****.*************.. *.  

206. spacer 12.69|6227843|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP025552 (Streptomyces rimosus strain WT5260 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

ccaaccacccgccggaactccaacaagcgt	CRISPR spacer
ttcgccacccgccggaactcctccaagggc	Protospacer
.. .*****************  **** *.

207. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP021282 (Legionella pneumophila subsp. pneumophila strain Flint 2 (D-7477) plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
ttgccagaatttaataactcaacagctaaa	Protospacer
.  .* .*****.*.***************

208. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP016031 (Legionella pneumophila strain OLDA plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
ttgccagaatttaataactcaacagctaaa	Protospacer
.  .* .*****.*.***************

209. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NZ_LT598658 (Legionella pneumophila strain Lpm7613 isolate Lpm7613 plasmid 2) position: , mismatch: 8, identity: 0.733

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
ttgccagaatttaataactcaacagctaaa	Protospacer
.  .* .*****.*.***************

210. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NZ_LN681226 (Legionella hackeliae strain ATCC 35250 plasmid II, complete sequence) position: , mismatch: 8, identity: 0.733

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
ttgccagaatttaataactcaacagctaaa	Protospacer
.  .* .*****.*.***************

211. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP021287 (Legionella pneumophila subsp. pneumophila strain Albuquerque 1 (D-7474) plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
ttgccagaatttaataactcaacagctaaa	Protospacer
.  .* .*****.*.***************

212. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP004007 (Legionella oakridgensis ATCC 33761 = DSM 21215 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.733

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
ttgccagaatttaataactcaacagctaaa	Protospacer
.  .* .*****.*.***************

213. spacer 12.72|6228071|30|NZ_CP042437|CRISPRCasFinder matches to NC_006365 (Legionella pneumophila str. Paris plasmid pLPP, complete sequence) position: , mismatch: 8, identity: 0.733

cattctaaatttgacaactcaacagctaaa	CRISPR spacer
ttgccagaatttaataactcaacagctaaa	Protospacer
.  .* .*****.*.***************

214. spacer 12.73|6228147|30|NZ_CP042437|CRISPRCasFinder matches to NZ_AP018204 (Leptolyngbya boryana NIES-2135 plasmid plasmid1 DNA, complete genome) position: , mismatch: 8, identity: 0.733

tgaggaaaaattaggttatggtgcatcatt	CRISPR spacer
ccaggaaaaattaggctatggtccaacgca	Protospacer
. *************.****** ** *.. 

215. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to CP003185 (Thermoanaerobacterium saccharolyticum JW/SL-YS485 plasmid pMU3262, complete genome) position: , mismatch: 8, identity: 0.733

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
tgaaatttcttcacataaatcaaaagattt	Protospacer
  *****  ****************.   *

216. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to NC_019956 (Thermoanaerobacterium thermosaccharolyticum M0795 plasmid pTHETHE01, complete sequence) position: , mismatch: 8, identity: 0.733

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
tgaaatttcttcacataaatcaaaagattt	Protospacer
  *****  ****************.   *

217. spacer 12.80|6228679|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP040048 (Acinetobacter baumannii strain VB1190 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

acatttctttttggactttaaccattacag	CRISPR spacer
gcatttattttttgactttaaccactctta	Protospacer
.***** ***** ***********.* . .

218. spacer 12.80|6228679|30|NZ_CP042437|CRISPRCasFinder matches to KY883640 (Vibrio phage JSF17, complete genome) position: , mismatch: 8, identity: 0.733

acatttctttttggactttaaccattacag	CRISPR spacer
gaatttatttttggactttaatcatcccga	Protospacer
. **** **************.***. *..

219. spacer 12.84|6228983|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP021356 (Rhodococcus sp. S2-17 plasmid pRB29, complete sequence) position: , mismatch: 8, identity: 0.733

taaccgcaatttcgggactgccgcgcttgc	CRISPR spacer
ccaccgcaatttcgggaccgtcgcgaagga	Protospacer
. ****************.*.****   * 

220. spacer 12.89|6229363|30|NZ_CP042437|CRISPRCasFinder matches to MN035857 (Leviviridae sp. isolate H2_Bulk_36_scaffold_96 hypothetical protein (H2Bulk3696_000001), hypothetical protein (H2Bulk3696_000002), and RNA-dependent RNA polymerase (H2Bulk3696_000003) genes, complete cds) position: , mismatch: 8, identity: 0.733

atacaacagacaattacaatacaatcggtt	CRISPR spacer
ggtctcaagacagttacaacacaatcggtt	Protospacer
.  *   *****.******.**********

221. spacer 12.95|6229819|30|NZ_CP042437|CRISPRCasFinder matches to MN693433 (Marine virus AFVG_25M397, complete genome) position: , mismatch: 8, identity: 0.733

cctctcaaaatctcaaaacgacgcattagg	CRISPR spacer
aattagaaaatcacaaaacgaggcattaga	Protospacer
  *.  ****** ******** *******.

222. spacer 12.95|6229819|30|NZ_CP042437|CRISPRCasFinder matches to AP018399 (Xanthomonas phage XacN1 DNA, complete genome) position: , mismatch: 8, identity: 0.733

cctctcaaaatctcaaaacgacgcattagg	CRISPR spacer
tctacaaaaatctcaaaacgatgcattgat	Protospacer
.** . ***************.*****.. 

223. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP034079 (Pseudomonas syringae pv. pisi str. PP1 plasmid pPP1-1, complete sequence) position: , mismatch: 8, identity: 0.733

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
gcagagccaagcaccagcaggaagaccaga	Protospacer
. . ****** ************ ****. 

224. spacer 12.96|6229895|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP015623 (Corynebacterium crudilactis strain JZ16 plasmid pCRULAC1, complete sequence) position: , mismatch: 8, identity: 0.733

aagtagccaaccaccagcaggaacaccaac	CRISPR spacer
cagtagccaaccaccagcgggacagtctaa	Protospacer
 *****************.***  ..* * 

225. spacer 12.97|6229971|29|NZ_CP042437|CRISPRCasFinder matches to LR134125 (Klebsiella aerogenes strain NCTC10006 genome assembly, plasmid: 5) position: , mismatch: 8, identity: 0.724

atttaactggtgcccgtttaattaaagag	CRISPR spacer
caggaactggtacccgtttaattaatcgg	Protospacer
    *******.*************  .*

226. spacer 12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MT496971 (Escherichia phage Mt1B1_P10, complete genome) position: , mismatch: 8, identity: 0.733

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
gtaccaatgctaatagcaatagctggaaca	Protospacer
**************.*****.**..*.  .

227. spacer 12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MT496971 (Escherichia phage Mt1B1_P10, complete genome) position: , mismatch: 8, identity: 0.733

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
gtaccaatgctaatagcaatagctggaaca	Protospacer
**************.*****.**..*.  .

228. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP022644 (Bacillus wiedmannii PL1 plasmid pBwiPL1-1 DNA, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacatgtc	Protospacer
************ * *********   .  

229. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP012101 (Bacillus thuringiensis strain HS18-1 plasmid pHS18-2, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacatgtc	Protospacer
************ * *********   .  

230. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP016596 (Bacillus cereus strain K8 plasmid pBCM301, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacacgtc	Protospacer
************ * *********   .  

231. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP018741 (Bacillus cereus strain FORC_047 plasmid pFORC47_1, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacatgtc	Protospacer
************ * *********   .  

232. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP029455 (Bacillus cereus strain FORC087 plasmid pFORC087.1, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacacgtc	Protospacer
************ * *********   .  

233. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP010112 (Bacillus thuringiensis serovar indiana strain HD521 plasmid pBTHD521-6, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacacgtc	Protospacer
************ * *********   .  

234. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_018688 (Bacillus thuringiensis MC28 plasmid pMC319, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacatgtc	Protospacer
************ * *********   .  

235. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP045608 (Bacillus cereus strain SB1 plasmid p2, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacatgtc	Protospacer
************ * *********   .  

236. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP009336 (Bacillus thuringiensis strain HD1011 plasmid 1, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacacgtc	Protospacer
************ * *********   .  

237. spacer 12.110|6230956|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP016590 (Bacillus thuringiensis strain KNU-07 plasmid pBTKNU07-02, complete sequence) position: , mismatch: 8, identity: 0.733

gaggctaaaatacaagtaaagacagcaaaa	CRISPR spacer
gaggctaaaataaatgtaaagacacatgtc	Protospacer
************ * *********   .  

238. spacer 12.112|6231108|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_011412 (Clostridium perfringens plasmid pCP8533etx, complete sequence) position: , mismatch: 8, identity: 0.733

tgacttagttaacaggccagaacttgcatt	CRISPR spacer
agcattagttatcagggcagaacttgctaa	Protospacer
 *  ******* **** **********   

239. spacer 12.112|6231108|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_007773 (Clostridium perfringens plasmid pCPF5603, complete sequence) position: , mismatch: 8, identity: 0.733

tgacttagttaacaggccagaacttgcatt	CRISPR spacer
agcattagttatcagggcagaacttgctaa	Protospacer
 *  ******* **** **********   

240. spacer 12.113|6231184|29|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MN694669 (Marine virus AFVG_250M354, complete genome) position: , mismatch: 8, identity: 0.724

aataatatacaatcctaaatccaggctgt------	CRISPR spacer
aataatagacaatcctaaatc------atttaaaa	Protospacer
******* *************      .*      

241. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP014289 (Bacillus thuringiensis strain Bt185 plasmid pBT1850046, complete sequence) position: , mismatch: 9, identity: 0.7

accaccccttttttttaaaaaaaagggaac-	CRISPR spacer
-tttccctttttttttagaaaaagggaaata	Protospacer
 .. ***.*********.*****.**.**. 

242. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NC_007392 (Spiroplasma citri plasmid pSci6) position: , mismatch: 9, identity: 0.7

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
taaattaattttttttaaaaaaatgggaat	Protospacer
   *..  *************** *****.

243. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NC_018146 (Zymomonas mobilis subsp. mobilis ATCC 29191 plasmid pZZ6.01, complete sequence) position: , mismatch: 9, identity: 0.7

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
ttaagaattttttcttaaaaaaaagggaaa	Protospacer
 . *   .*****.*************** 

244. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to MF974396 (Leptospira phage LE3, complete genome) position: , mismatch: 9, identity: 0.7

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
atatcccctttcttttaaaaaaaagatcgg	Protospacer
*.  *******.*************.  . 

245. spacer 12.8|6223212|30|NZ_CP042437|CRISPRCasFinder matches to MH673674 (Thermus phage phiMa, complete genome) position: , mismatch: 9, identity: 0.7

ggttgggatataagtcaaaacccttcaaag	CRISPR spacer
atgggggatataagtcaatacccttagttg	Protospacer
.   ************** ****** .  *

246. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MH853788 (Acinetobacter phage vB_KpnM_IME512, complete genome) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
ttgggtttacaataaaaaagccttgttgct	Protospacer
  ******* *************... . *

247. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK448711 (Streptococcus phage Javan235, complete genome) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
cccaatctaaaataaaaaagccacacaaac	Protospacer
   ..*.*************** *****..

248. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK448893 (Streptococcus phage Javan270, complete genome) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
tgaatattaaaataaaaaatcctcacactc	Protospacer
 *..  ************* *******  .

249. spacer 12.15|6223744|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP014858 (Vibrio phage RYC DNA, complete sequence) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
gtttatttaaaataaaaaagccccactcct	Protospacer
.   .*****************.***   *

250. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_023571 (Oenococcus phage phiS11, complete genome) position: , mismatch: 9, identity: 0.7

taaagaagatgatgtaaattttgccgatcg	CRISPR spacer
aggcacagatgatgtaaatttttccaatca	Protospacer
 .. . **************** **.***.

251. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_023559 (Oenococcus phage phi9805, complete genome) position: , mismatch: 9, identity: 0.7

taaagaagatgatgtaaattttgccgatcg	CRISPR spacer
aggtacagatgatgtaaatttttccaatca	Protospacer
 .. . **************** **.***.

252. spacer 12.17|6223896|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_023560 (Oenococcus phage phiS13, complete genome) position: , mismatch: 9, identity: 0.7

taaagaagatgatgtaaattttgccgatcg	CRISPR spacer
aggcacagatgatgtaaatttttccaatca	Protospacer
 .. . **************** **.***.

253. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MH853788 (Acinetobacter phage vB_KpnM_IME512, complete genome) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
ttgggtttacaataaaaaagccttgttgct	Protospacer
  ******* *************... . *

254. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK448711 (Streptococcus phage Javan235, complete genome) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
cccaatctaaaataaaaaagccacacaaac	Protospacer
   ..*.*************** *****..

255. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MK448893 (Streptococcus phage Javan270, complete genome) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
tgaatattaaaataaaaaatcctcacactc	Protospacer
 *..  ************* *******  .

256. spacer 12.24|6224427|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP014858 (Vibrio phage RYC DNA, complete sequence) position: , mismatch: 9, identity: 0.7

aggggtttaaaataaaaaagcctcacaagt	CRISPR spacer
gtttatttaaaataaaaaagccccactcct	Protospacer
.   .*****************.***   *

257. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP013982 (Staphylococcus equorum strain KM1031 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.7

ccacgtagatatatataaagatttttacct	CRISPR spacer
ccaggtagatatatataaagaacaatcaaa	Protospacer
*** ***************** .  *    

258. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP013982 (Staphylococcus equorum strain KM1031 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.7

ccacgtagatatatataaagatttttacct	CRISPR spacer
ccaggtagatatatataaagaacaatcaaa	Protospacer
*** ***************** .  *    

259. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP013717 (Staphylococcus equorum strain C2014 plasmid pC2014-3, complete sequence) position: , mismatch: 9, identity: 0.7

ccacgtagatatatataaagatttttacct	CRISPR spacer
ccaggtagatatatataaagaacaatcaaa	Protospacer
*** ***************** .  *    

260. spacer 12.36|6225339|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NC_015708 (Pseudoalteromonas sp. SANK 73390 plasmid pTML1 carrying thiomarinol biosynthesis cluster) position: , mismatch: 9, identity: 0.7

tgtttttgttacataaattgtataccctgc	CRISPR spacer
cgtatttcttacataaattgtatattgcat	Protospacer
.** *** ****************.. ...

261. spacer 12.44|6225947|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to MF042360 (Pseudomonas phage Phabio, complete genome) position: , mismatch: 9, identity: 0.7

tatgatatcgaagtattgaacgatagtata	CRISPR spacer
gtggatatcgaacaattgaacgatagctcg	Protospacer
   *********  ************. ..

262. spacer 12.55|6226782|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.7

ggtacccagtacggccaccagggcattatt	CRISPR spacer
aagacccagtacggccacccggccatcgac	Protospacer
.. **************** ** ***.. .

263. spacer 12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT151955 (Brevibacillus phage Jenst, complete genome) position: , mismatch: 9, identity: 0.7

ttggcacaatgctaagattgatgatataat	CRISPR spacer
cgatgtcattgctaagattgatgaaataaa	Protospacer
. .   ** *************** **** 

264. spacer 12.60|6227160|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to KT151957 (Brevibacillus phage SecTim467, complete genome) position: , mismatch: 9, identity: 0.7

ttggcacaatgctaagattgatgatataat	CRISPR spacer
cgatgtcattgctaagattgatgaaataaa	Protospacer
. .   ** *************** **** 

265. spacer 12.68|6227767|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to NZ_CP024200 (Thalassospira marina strain CSC3H3 plasmid pCSC3H3, complete sequence) position: , mismatch: 9, identity: 0.7

gcgccaatgataatggcaatggcaaggaga	CRISPR spacer
atgccattgataatggcaatggcggcaatg	Protospacer
..**** ****************.. .* .

266. spacer 12.75|6228299|30|NZ_CP042437|CRISPRCasFinder matches to HM144387 (Bacillus phage W.Ph., complete genome) position: , mismatch: 9, identity: 0.7

acaaattaattcacataaatcaaaaacaat	CRISPR spacer
gtttgttaattcacttaaatcaaaatcagc	Protospacer
..  .********* ********** **..

267. spacer 12.95|6229819|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.7

cctctcaaaatctcaaaacgacgcattagg	CRISPR spacer
gtcttcaaaatcgaaaaacgacgcatttta	Protospacer
 ...********  *************  .

268. spacer 12.101|6230273|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to EU545650 (Acidianus filamentous virus 9, complete genome) position: , mismatch: 9, identity: 0.7

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
ctagcaatgctaatggcaatggagacaaaa	Protospacer
 ** ******************  * . ..

269. spacer 12.106|6230653|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to EU545650 (Acidianus filamentous virus 9, complete genome) position: , mismatch: 9, identity: 0.7

gtaccaatgctaatggcaatggccaggcgg	CRISPR spacer
ctagcaatgctaatggcaatggagacaaaa	Protospacer
 ** ******************  * . ..

270. spacer 13.1|6453774|34|NZ_CP042437|CRISPRCasFinder matches to MK552327 (Pseudomonas phage Psa21, complete genome) position: , mismatch: 9, identity: 0.735

---ggttcacttgttcattagttcatcggtctttgcg	CRISPR spacer
aaaagccca---gttcattatttcatcagtctttgct	Protospacer
   .*..**   ******** ******.******** 

271. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to MF974397 (Leptospira phage LE4, complete genome) position: , mismatch: 10, identity: 0.667

accaccccttttttttaaaaaaaagggaac	CRISPR spacer
gtaccccctttcttttaaaaaaaagattgg	Protospacer
..  *******.*************.  . 

272. spacer 12.31|6224959|30|NZ_CP042437|CRISPRCasFinder,PILER-CR matches to AP013402 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-U-MedDCM-OCT-S38-C27) position: , mismatch: 10, identity: 0.667

ccacgtagatatatataaagatttttacct	CRISPR spacer
gatgaaagatatatataaagattattataa	Protospacer
    . ***************** ***.  

273. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to NZ_CP006906 (Clostridium baratii str. Sullivan plasmid pCBJ, complete sequence) position: , mismatch: 12, identity: 0.6

accaccccttttttttaaaaaaaagggaac--	CRISPR spacer
--ggcttttgttttttaaaaaaaaggtgtggt	Protospacer
   .*...* **************** .    

274. spacer 12.5|6222985|30|NZ_CP042437|CRISPRCasFinder matches to MK911750 (Streptococcus phage P738, complete genome) position: , mismatch: 13, identity: 0.567

accaccccttttttttaaaaaaaagggaac---	CRISPR spacer
---gttccgttttttttaaaaaaaaaagtcaaa	Protospacer
   ...** ******* *******.... *   

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	4021626 : 4031204	10	Caulobacter_phage(50.0%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP042437|4021626:4031204|DBSCAN-SWA
ACTATTTATCCCTGGTAAACAAATAGGTTTCACCATTTTGAAAGTAATAAAAACTGTGCTTAACGGTATCAAACCGAAGTGAAACCCCTGCCAAATCCAGTACGAATTTATCGTTACCCCTGGCCTCGAGCGGATAGGCGCTTTGGCCGGTGGCTTGCCCTATCAGCGTTGTTTTGTTTTTAGTAATAGCTATTTTTAGGGGCATTTTAACGCTGGAGTAATTGCCGAGGTACTTATCCAGATCGGCACTTTTAAGCTCAACGCTCTTAAATTCGGGCATTGCAAAGGGCTTATTATAATAAATGCTCAAAGCATCCGCGACAATCTCATTAGTAGGATACCGGATACCGTTGGCTATGTAAGCCACCGACAGCTTATCGGCCGGGTAATAAATAAGCTGACTCAAAAATCCGTCGATACCGCCACTATGGCCATAACCTGTTTTATCATCAAAGGGAAAAATAAACATCGCCATACCAAAATTATCCTTCATCAGTTTCATGTGCTCCAAATTTGTGTTGCTGATGAGTTTGCCGGCAAAAAGTGCGTCGATAAAGTGAACCAGGTCGGTAGGTGAAGCTACAATGGCTCCTGCGCCGCCCGGAATACTCATGTCTGTTTCGGGCACCTGGCTCCATCCAGAGATGTAGTTATAGGAATAAGCTTCATCATTTAACGAATCGGTTTTAGTGCCATAATAAGTATCTTCCAATCCTATTTTGGTTGTAATGCGTTCCTTCAGTTCTTCGGGATAGCTTTTACCAGTAATTTTTTCGATGATATAACCCAGCAGTACAAAATTTGTATTGCTATACGCGGCTTTAATGCCGGGCTCAAAATCGGCTTTCTGCTTTGCAAAAATGGCTGTCATTTCCGCTTCAGATTTCGGCTTGCCCATATAGTTAAGATAACCCGAATCAGCGGTGAAATTATGAAGCCCGCTGTGGTGGCTCAGCATTTGGGCAATAGTAATCTTGCCTGCATTGGGTAATTGCGGGTAATACTTAGCCAATGTAGTAGTTAGCGTAAGCTTACCCTCTTCAATAAGCTGAAAAATCATAACAGCGGTGAACATCTTGGTGATAGACCCCACCCTGTATTTGGTATGAACATTTGCCGGCGTTTTAATAGTGCCATTTATTCGGCTGTAGCCAAAAGCCTTTTGGTAAACAATCGTTCCGTTATCTGCTATCGCGATGCTACCCATATTCTGCTCATGCGCATTCAGCGTAACCAGTAAGGTGTCTAACCTGGGTTTATTAAAACTATGTTTATGGCAGCCCGATAGCAAGGCCAATATTGGCAATAAAATAAAAAGCAGTTTTCGGATCATTTTTGCAATAGTTCAGGTGACAAAAGCAATAACGTTTGTTGTGCAACTGTATTGCGTGGCGGTTTGTTTAAACAGGTGATTGCTTTAAATGCCCTTGTTGAAAGGTATACGTCATGCTAAAACGGATTAGCAAATGTATTAATGGTTTAATAATACCCATGCTAATAAGTAAACCTTATGCTAAAACGATTTTAGCCTTCGCCAATAGCATGCCCTTAGTTTATGTTCGATATTGACGTATACCGGCCCGCGCCCGATGCCAGGTGCCAGCGTCTGGCCCGGCCAGCTTTCTGACGGGCTTTTGCCCTGCGGGAGCAGTCTGCAAATTCCTTCGCATCATAGGCATCGGACCTATAGGGCGTACCCTTTTCGGGGAATAGGGCGGGTTGGTTCCTTCATTTTTATTTCATACTGTATATCAAAAAAACATATACCTTAGTTGTGCATTTTAAACCTTAGTTAAGCAAAATTTGAGGCCATTTTCGTAACAATTACGCGGCCTGCTTGTCAATATATAAATACATTTTACAATGGCTATTAATCTTCAAAAAGGACAAAAAATAGATATCGGACTGTCGAAAATGACAGTTGGTTTGGGCTGGAACCCAAATGAAGGCACAGGTTATGATTTCGACCTGGACGTATCGGCTATCATGATAGATGGCAACAGGTTTGTACCTGAAGACGAATTTTTCGTTTTTTATAACAACGTAGATTCGCCTGACGGCGCTGTTCATCACACCGGCGACGATCCTTCGGGCGGCAACAGCGATGGCGGCGATGATGAATCTATCAATATTGATTTAACTAAAGTTGATGGTAAAATACAGGAGATATTGTTTGTGGTAACCATTCACGAAGCACAGCCCCGCAGGCAAAACTTTGGCCAGGTGCGCGATTCATACATTCGCATTATTGATGAGCAAACCGGCAGCGAAGTTTGCAAATATGAGTTGGGCGAAGATTTTTCTATCGAAACAGCTATTGAGTTTGGCCGTTTATACCGCCGTAACGGCGCCTGGAAGTTTGAGGCATCGGGCGTGGGTTACAAGGAGGATCTTGCCTTCTTTTTAAGCAAGTATTTTAAGGGGCAAATTATTAAATAACAAGGGGCGTCCCCACCCAACCCTCCCCGGAAGGGGGCTGGCTTTTATTGATTAACAATATTATTATGGCAATTAATCTGGTTAAAGGTCAAACAATTGATCTTCGTAAAAATGATAAGGGCGAAAGCTTCGACCTGTCGTCGGTGACCATTGGCTTAGGCTGGGATGTAAGGCAAAGCCGCGGTGGCGGCGGTTTTTTGGGCAAACTATTTGGCGGCGGCGGTGAAGAAGTGGAGTATGACCTGGATGCTATAGCTTTCCTGCTGGATAAAAACGGCCATGTGGCCAACAGGGGCCGCACGTTTCAAAAACCCAACGGCAACAAAATAAATTTATATGAGGGCGATGTGGTTTATTTTAACTCCATGCGCCATCCATCAAACCATATCTGGCTTACGGGCGATAACCGTACAGGCGCTGGCGCTGGCGATGATGAGCAAATCATCGTGAAACTGGATGCGCTGGATCCGAAATACGATCGCATCCTGTTTATTGTAGCCATATACCAGGGCCAAAGGAAAAATCAGCATTTTGGCATGGTCGAGAATGCCTTTATCCGCGCTGTTGACAACCATGGCAAAGAGATAGCCAAATTCAGCCTGTCGGGCGATGCCACCTACAACGGTATGTGCTCCATGAAATTTGCCGAGGTATACCGTAAAGACGGAACCTGGAAATTCCGCGCCATTGGCGAACCATTTGCAACGGATAATTTTTTGGAACTACTTAAACAGTATTGAATTGGGTTGTACGTTGTAAGTTATACGTTGTACGTGCCTGTTTGGTAAAAAAACGTGTAGCTTACAACATATCGCGTACAACCTATATTTATAATGGCTAACAATATTGAAAATTTTGTTGTACATCTATATTTGCTAATTAGGCAAAACGTATAACTTACAACGTATCACGTACAACCTACACGGCCTGCAATGTACCAACACTACTCCTTCGATCTTTGGCTTACGCTGATCAAATCAAATCCATATTTTAAAATAGAGCGTACCAAAATCTTTCACCGGGATTTTAATCCTGCAGGTAAAAGCATCGACGAGGTGGCCAGGGCTTTCAGGCAGGTGGATTTGATGTGCAACGCGGTGAATGAAAACACAGGCAAAAACATTGATGCCGATGAGATGTACCTGATGGTGATTAGCCTGATTAATGACAATCAGCTCAGCTTATCAGATATTGATACCGGCAAACTGTACCAGGATATGGAGAAGCTGTTGTTTTACTACTTGCCGCTGGTATACTCGCCTGTAACAATTTCCACGTTGCAGCATCTAAAAGATAAAACAGGTAGTACCTTTAGTTTGTTAAGCAATACCGGTTTTATAAAGGGGGCAACCTTAAGAAAGGTACTGGTGGAATTAAAGATGAGCAATTACTTTGATTTTCAACTGTACTCAGACGAGGTGGGGATGTCGAAGCCAAACCCGGCCTTGTTTAATTTAATGCTGCAAAACATCAAACAGGTTAACACCCATAAGGATATCAATTTAACTGATATTATACATATAGGCGATAACCCTAAAGCTGATATTGACGGTGCACTTGCGGCCGGTATAAAAAGTTTGCTTATCAATTCAAACAACCAATCTATTTTAGCCTTATTAAGCTAATGAACGCTACCTACTCATTACATCATGTTGATAACGATAGCAGCTTCGGCTTTTGCCCGGATAGCTACAGCCGTTTCAAATTTGGGGATGAAGCCGTAGCCCGGAAATTTGGCTGCGCTTTAGCGGATGGTTTTATTGGGCATATTTTATCAAAACAACCCATCACGCAGCAAATTGTGGTGATATCAAGCCCTTACTCGTTTATCCCAACAGCTACCTTTGCCATGAAAACATGGTTTGTATACGGCCTTAACCGCTGGCTGGCACAACACGGATACGCAGTAGTGCAGGAAACCAAGGTACACCGCACCATTACGTATAAGGAAGATTATGGCGAACTGAACGCCGAGCAAAGAATGAACCTGATAGGGAACGACTCATTCCATATCGACAAGGATTTTTTGACCGGTAAAACGCTGATATTTTTAGATGATATTAAAATAACCGGCAGCCACGAGCGCATGATCATGAAGATGGTGGATGCATACGGCCTGAGCAATGATATTTATATGCTGTACTTTGCCGAGCTGGTGAATAAAACCATCCACCCCAACATCGAGAACTTTTTAAACTATCACCAGGTAAAAACTATTTTCGACCTGGAGCCCATTATACAAAGCGGCAACTTTGCTATTAATACCCGGATAGTTAAATATATATTGAATTACAATCCCGATTGCTTTAGTATTTTTATACAAAACCAAACAATGGATTTTGTAAACTTGCTATATGATATGGCTTTGGGCAATGGCTACCATACTATTGATGCCTATGCCCAAAACCTTAACTTTATTACCAAAAACCTATTTATAAACAATAAAAATCTGATTAAACATGGCAATTAATTTGCAAAAAGGCCAGCGCGAAAGCATCCACGCCCCCAAATTTACTATAGGGCTGGGCTGGGATACCAATAGCTCATCAACAGGCAGCGCGTTCGATTTAGACGCATCTGTTTTTATTTTGGGCGACAATAAACGATTACTGGCCGACGAATATTTTGTGTTTTATAACAACCTGGTATCCCCGGATGGCGCGGTTGAGCATACCGGCGATAACCTTACCGGCGCGGGCGATGGCGATGACGAGCAGGTAAAGGTCGATCTGTCTAAAATTTCCCCGCAGGTATCTGAAATTTGTATAGTAGTAACCATCCATGAGGCCGAAGCACGCAGGCAAAACTTTGGCCAGGTGCGCAACTCATTCATCAGGATATTTGATGCCGAAACAGGTGCCGATATTTTGAAATATGAGCTGGAAGAAGATTTCTCGATAGAAACCGCTGTTGAGTTTGGCCGTATTTACAAAAAAGATAATAACTGGAAATTTGAAGCTGTTGGCGTTGGTATGAAAGGTGGCCTGCAGGATTATTTAAACAAATATCAATAACGGCTATGGCAATTAATCTTCAAAAGGGACAACGCATCAGCCTCGAAAAAAGTAACGGCAGCAAATTACAAAGTGTTTGCGTGGGTATTAACTGGGGAGCCATTGAAAAAAAAGGCCTTTTTGGCTTTGGCGTAACCAAAGAAGCGGTTGATCTTGACGCCAGTTGCGCTTTGTTTGACGAAAGCAAACGCCTGGTAGATGTGATCTATTTCGGCAATTTAAAATCAAAAGATGGCTCGGTAAAACATAGCGGCGACGACCTTACCGGCGATTTAAACGGCAACGACGGTATTGACAATGAAGTAATTACTGTAAACCTTCCGGGTTTGCCTGCATCGGTAGCCTATGTAGCATTTATGCTGAACAGCTTTCGCGGACAGGATTTTGGTACTATTCCTTTCGCCTCCATCCGCATTTATGAAGGTACACCAACCCGTGTAAACGAAGTGTTTGCTACCTATGATATTGCACACAGTAAAGATTTTGCGGGCCACGTTGCCATGGTTATGGGCGTTTTTTACAAAAAGAACGGCGAATGGAAATTTAATGCCATTGGCGAACCAACCCGCGACCGCAAACTGGAAGAAACCGTTAAAACAGTTACCAATAATTATTTATAGTGAGTTGGTGAGTGGTGAATAGTGAGCAGTGAATGGTAAGTATAGAAGCATATCAACACTAACTAACTAACTAACTACACACAACTGACCATTCACCACTCACGACTGACCAAAATCACCATTAAAAACGCAAGAAAATGGAAGGCGCACCAAATAACACCCCGATAAATATAACCCCGGTTAACCTGGATATAACTCCGGCACCGGGAACAACCACTCCTGTAAAATTACTGGATAAGGAGGGTAATGTAGATTTAACTAACATTACGCCTACCGAAGTGCAAAAGTACAGTGAAGTAGCCAAGGCTCTTGACCCTAAGGATGTTAACTCCATCCTTAACTATGGCACTGATGTGCAGGCATCGATGGAGAAGTATAGTAACAACTTTTTAACTTCGGTACGTACCTATAACTCCGGCGAAGTTGGTTTGCTGATAAACGACCTGCTTACCGAACTGAACTATATTGACGTAGATGAGCTGAACCAAAACGCGTTCACCTCGTTTATCTCCCATATCCCTTTCATGAAAAAGCTGGTATTTGATGCCAAAAAACTATTTCAGAAGTACGATACGGTGATTAACAACATCGATAAGATCACCAATAAGATTAAGGCAGGTAGGGTTAACTCACTGAAGGACAATAGTTCGTTGCAAACTATGTTTGACAGCAACGTGACTTACATCCACCAGATGGAAGAGCTGATCATATCCGGTCAGTTAAAATACAATGAACTGAGTGAGCAATTGGCGCAAATGGATGCCAACCCATCGGCCTATAACGATTACGAAATTGCCGACCTGCGCGATTTTGTGAATCGCCTTGATAAACGCCTTGCCGACTTGAAAGTAGTAAGGTTTATCATGATGCAATCATTGGCACAAATACGCGTGGTGCAAAGTAATAACACTACCATAGCCGAGAAAGCACAATCCATCGTATCAACCACCATCCCGGTTTGGAAAAATCAGCTTACGATAGCTGTTGCCCTGAACCGCCAGAAGGAAAATGTGGAGATGCAGAAAAAGATCTCGGATACAACCAACACCATCCTGCAAAAAAATGCCGAGCTGCTTAAACAAAACAGTATTGACGTTGCCCGCGAGAATGAGAAAACGGTAGTATCGCTGGATACCCTGAAACGCACAACCGCATCGCTGATTGAAACCCTTACCGAGGTAAAACGTATTCATGATGAAGGTACTGCCAACAGAAAGGTACTTAACACCGAATTGCAGACACTGGAAACAGAGTTGAAAAAGCATGTGACTAACGCGTAAGCGAAGTCCCATCATCTCTTTATGTCATTGCGCGTATCCATCCGGTAAAACCTGAAAAAGATCGTTATGACGTGCAAGGGATATAAGTTAAACGAATGCTCTAAACTACCGTCATTGCGAGGTACGAAGCAATCCCGAACTATGTGGGACTAAGCATGTAGGGGATTGCTTCGTGGCAATGACGGATATTTTATAGTGACAGTCAATAACTTACAAACACGTCATTATAAGGAACGCAGCAATCTCGAATCTTGCACACACTGCACAGTTCGCGATTGCCGCGCTGCGCTCGTAATGACTTAATTTCCCCATCGCCTGTGTCTTCACAGGCGATTTGCATTTAAAGGCCTCGCCTTCAGGGTAGGGTTTGGGTGGGGTTTCTTTTTTCGTAAATTTGTTCCTTCTCCATGGACGAAAACAGGTTAAATATTTTAAATCAGAGTAACCGGATGCTCAGTAAGCTGCAACTGCTTTCTGTATTTTTTGGCGACGATATGATTTATAAAATTTACCTGCGCAGCCAGGTAATCCATAAACTGTTTGAGGCCAATCCCGAGCTTGATATCAATAAACTCGACCTGTTCCACCTACAGTTTACCCAAAGCCTCATAGATTTGCTCCGGAAGATCAAAAAGAACAACGAGACCAATGTAAGCCTGTTGTTTGATGAAATTCAGATTAACCGCGAGATGATTGAACGGCTGAACGACCCCACTTATACCCTGGCAAACTTTAACCTTGAAAAGCAAAGGCAGGCGCTCAAGATCAACTTATCGTTACGAAAGCTATTCCAGGTATTGTCGGATAGTTCAACAGAAAACCCACTGTCTAAAAACATCAACGCGTTTAGCTCAAGGTTTGCGGCCGATTTTTTTTACACTATCAGCACCGACCTGATGGAAGAGGTTACGGCCTTTAACCTAACGGACGTTTACAAAAATGAATACGCCAAAATTCAGCGTAAGCTGATGGGGGTGTTGTGCAAATATGATTTTAAAACAGAGTTTTATTGCGGTTTAAAATCAGGAGCGCAGGTTATCGAGGTTTACAAATTTATTGAGGCCGATAGGTATTTTATATATGCCCCCGGCGATAACCTGTTTGTGTTTTTTGACGTGGCAAAAATAGCCGGGCTGGATATGACCACCAATATGTCGAAAAAAGAGCGGCTGATGTATGAACTCAAAGACAAAAACGACAGGCTTGAGGGCAACGCCGCTGCGATGAAAGCTCATATGCCGCCGGAAATTGCCGCCCTGCTTGCCGATAATTATAAAAAGATCTCGGATATTACCTTCCTTGATAATATCAGCAATATCGATGTGCAAGCCAATATTTTAAAAAGCATGCTCAATACCGATTTAATTTAGTTTATTTAACCTTAACAAAAATACATTACCTGTTTATATGGATTTACATACAATATTAGGCCCCGATATTAAAGCCGGCCTGCTCATTATTTTAAACCTGATCCTGATAGAGAGTTTGCTATCTGTAGATAATGCCGCCGTGCTTGCAACCATGGTGCTCGATCTTCCTAAAGATCAGCGTAAAAAAGCTTTACGTTATGGTATCATTGGCGCTTATGTATTGCGGGGTGTTTGTCTTTTCCTGGCCGCGTGGCTGGTAAAAATATGGTGGTTAAAACCCATTGGCGGCTTATACCTGTTATACCTTTGCTTTGATTATTTTAAAGGTAAAATTCAGGCTGCAAACGCAGGAGGCGAAGAAGAAGAGGTTGACAAAAGCAAAAACTGGCTATATAAATCAACAGTGGGTGTATTTGGGGTATTTTGGGCCACCGTTGCGCTGGTTGAATTAATGGACCTGGCTTTCTCTATTGATAACGTATTTGCTGCAGTAGCTTTTACAGATCATGTGGTTTTGATTTACATAGGCGTATTCATAGGCATACTGGCTATGCGTTTTGTTGCCCAGGCCTTTGTTAAGCTGATGGAGAAATTTACCTTCCTGGAAACTGTGGCATTTATTGTAATAGGTGTATTGGGTTTAAAATTATCGGCATCATTATATATCCACTTTTACCCGGAAACAGGTTTCTCTAAAATGATGGAAGGCGAGGGCGCCGATATAGCTACATCGGTATTTACAGTAGCCATATTTATTATACCTGTATTAACATCGCTGCTATTCAACTTCCCCAGGCGCCACACCATCGAACCGGAGGTAGCAGAAGCCGCGGAAGATGTTTTGGATAAGCAGTAG

Protein sequences of DBSCAN-SWA_1

>NZ_CP042437|4021626:4031204|4024129_4024804_+|WP_147055330.1|DBSCAN-SWA
MAINLVKGQTIDLRKNDKGESFDLSSVTIGLGWDVRQSRGGGGFLGKLFGGGGEEVEYDLDAIAFLLDKNGHVANRGRTFQKPNGNKINLYEGDVVYFNSMRHPSNHIWLTGDNRTGAGAGDDEQIIVKLDALDPKYDRILFIVAIYQGQRKNQHFGMVENAFIRAVDNHGKEIAKFSLSGDATYNGMCSMKFAEVYRKDGTWKFRAIGEPFATDNFLELLKQY
>NZ_CP042437|4021626:4031204|4027835_4028978_+|WP_147055341.1|DBSCAN-SWA
MEGAPNNTPINITPVNLDITPAPGTTTPVKLLDKEGNVDLTNITPTEVQKYSEVAKALDPKDVNSILNYGTDVQASMEKYSNNFLTSVRTYNSGEVGLLINDLLTELNYIDVDELNQNAFTSFISHIPFMKKLVFDAKKLFQKYDTVINNIDKITNKIKAGRVNSLKDNSSLQTMFDSNVTYIHQMEELIISGQLKYNELSEQLAQMDANPSAYNDYEIADLRDFVNRLDKRLADLKVVRFIMMQSLAQIRVVQSNNTTIAEKAQSIVSTTIPVWKNQLTIAVALNRQKENVEMQKKISDTTNTILQKNAELLKQNSIDVARENEKTVVSLDTLKRTTASLIETLTEVKRIHDEGTANRKVLNTELQTLETELKKHVTNA
>NZ_CP042437|4021626:4031204|4023488_4024064_+|WP_147055328.1|DBSCAN-SWA
MAINLQKGQKIDIGLSKMTVGLGWNPNEGTGYDFDLDVSAIMIDGNRFVPEDEFFVFYNNVDSPDGAVHHTGDDPSGGNSDGGDDESINIDLTKVDGKIQEILFVVTIHEAQPRRQNFGQVRDSYIRIIDEQTGSEVCKYELGEDFSIETAIEFGRLYRRNGAWKFEASGVGYKEDLAFFLSKYFKGQIIK
>NZ_CP042437|4021626:4031204|4030385_4031204_+|WP_147055345.1|DBSCAN-SWA
MDLHTILGPDIKAGLLIILNLILIESLLSVDNAAVLATMVLDLPKDQRKKALRYGIIGAYVLRGVCLFLAAWLVKIWWLKPIGGLYLLYLCFDYFKGKIQAANAGGEEEEVDKSKNWLYKSTVGVFGVFWATVALVELMDLAFSIDNVFAAVAFTDHVVLIYIGVFIGILAMRFVAQAFVKLMEKFTFLETVAFIVIGVLGLKLSASLYIHFYPETGFSKMMEGEGADIATSVFTVAIFIIPVLTSLLFNFPRRHTIEPEVAEAAEDVLDKQ
>NZ_CP042437|4021626:4031204|4027083_4027698_+|WP_147055339.1|DBSCAN-SWA
MAINLQKGQRISLEKSNGSKLQSVCVGINWGAIEKKGLFGFGVTKEAVDLDASCALFDESKRLVDVIYFGNLKSKDGSVKHSGDDLTGDLNGNDGIDNEVITVNLPGLPASVAYVAFMLNSFRGQDFGTIPFASIRIYEGTPTRVNEVFATYDIAHSKDFAGHVAMVMGVFYKKNGEWKFNAIGEPTRDRKLEETVKTVTNNYL
>NZ_CP042437|4021626:4031204|4025688_4026534_+|WP_147055335.1|DBSCAN-SWA
MNATYSLHHVDNDSSFGFCPDSYSRFKFGDEAVARKFGCALADGFIGHILSKQPITQQIVVISSPYSFIPTATFAMKTWFVYGLNRWLAQHGYAVVQETKVHRTITYKEDYGELNAEQRMNLIGNDSFHIDKDFLTGKTLIFLDDIKITGSHERMIMKMVDAYGLSNDIYMLYFAELVNKTIHPNIENFLNYHQVKTIFDLEPIIQSGNFAINTRIVKYILNYNPDCFSIFIQNQTMDFVNLLYDMALGNGYHTIDAYAQNLNFITKNLFINNKNLIKHGN
>NZ_CP042437|4021626:4031204|4024996_4025689_+|WP_147055333.1|DBSCAN-SWA
MYQHYSFDLWLTLIKSNPYFKIERTKIFHRDFNPAGKSIDEVARAFRQVDLMCNAVNENTGKNIDADEMYLMVISLINDNQLSLSDIDTGKLYQDMEKLLFYYLPLVYSPVTISTLQHLKDKTGSTFSLLSNTGFIKGATLRKVLVELKMSNYFDFQLYSDEVGMSKPNPALFNLMLQNIKQVNTHKDINLTDIIHIGDNPKADIDGALAAGIKSLLINSNNQSILALLS
>NZ_CP042437|4021626:4031204|4026523_4027078_+|WP_147055337.1|DBSCAN-SWA
MAINLQKGQRESIHAPKFTIGLGWDTNSSSTGSAFDLDASVFILGDNKRLLADEYFVFYNNLVSPDGAVEHTGDNLTGAGDGDDEQVKVDLSKISPQVSEICIVVTIHEAEARRQNFGQVRNSFIRIFDAETGADILKYELEEDFSIETAVEFGRIYKKDNNWKFEAVGVGMKGGLQDYLNKYQ
>NZ_CP042437|4021626:4031204|4021626_4022958_-|WP_147055327.1|DBSCAN-SWA
MIRKLLFILLPILALLSGCHKHSFNKPRLDTLLVTLNAHEQNMGSIAIADNGTIVYQKAFGYSRINGTIKTPANVHTKYRVGSITKMFTAVMIFQLIEEGKLTLTTTLAKYYPQLPNAGKITIAQMLSHHSGLHNFTADSGYLNYMGKPKSEAEMTAIFAKQKADFEPGIKAAYSNTNFVLLGYIIEKITGKSYPEELKERITTKIGLEDTYYGTKTDSLNDEAYSYNYISGWSQVPETDMSIPGGAGAIVASPTDLVHFIDALFAGKLISNTNLEHMKLMKDNFGMAMFIFPFDDKTGYGHSGGIDGFLSQLIYYPADKLSVAYIANGIRYPTNEIVADALSIYYNKPFAMPEFKSVELKSADLDKYLGNYSSVKMPLKIAITKNKTTLIGQATGQSAYPLEARGNDKFVLDLAGVSLRFDTVKHSFYYFQNGETYLFTRDK
>NZ_CP042437|4021626:4031204|4029385_4030348_+|WP_147055343.1|DBSCAN-SWA
MDENRLNILNQSNRMLSKLQLLSVFFGDDMIYKIYLRSQVIHKLFEANPELDINKLDLFHLQFTQSLIDLLRKIKKNNETNVSLLFDEIQINREMIERLNDPTYTLANFNLEKQRQALKINLSLRKLFQVLSDSSTENPLSKNINAFSSRFAADFFYTISTDLMEEVTAFNLTDVYKNEYAKIQRKLMGVLCKYDFKTEFYCGLKSGAQVIEVYKFIEADRYFIYAPGDNLFVFFDVAKIAGLDMTTNMSKKERLMYELKDKNDRLEGNAAAMKAHMPPEIAALLADNYKKISDITFLDNISNIDVQANILKSMLNTDLI

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_147055327.1|4021626_4022958_-	serine hydrolase	A0A076YS03	Mycobacterium_phage	1.6e-19	30.1
WP_147055328.1|4023488_4024064_+	TerD family protein	K4JRX3	Caulobacter_phage	2.0e-27	36.1
WP_147055330.1|4024129_4024804_+	TerD family protein	K4JRX3	Caulobacter_phage	1.1e-19	29.7
WP_147055333.1|4024996_4025689_+	HAD-IA family hydrolase	NA	NA	NA	NA
WP_147055335.1|4025688_4026534_+	hypothetical protein	A0A291LAE0	Escherichia_phage	3.0e-32	32.4
WP_147055337.1|4026523_4027078_+	TerD family protein	K4JRX3	Caulobacter_phage	1.2e-34	44.2
WP_147055339.1|4027083_4027698_+	TerD family protein	K4JRX3	Caulobacter_phage	4.6e-14	31.3
WP_147055341.1|4027835_4028978_+	toxic anion resistance protein	A0A1D7XGB3	Escherichia_phage	3.7e-09	22.6
WP_147055343.1|4029385_4030348_+	hypothetical protein	NA	NA	NA	NA
WP_147055345.1|4030385_4031204_+	DUF475 domain-containing protein	A0A068EP98	Bacillus_phage	1.7e-32	45.1