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_CP014263	Spirosoma montaniterrae strain DY10, complete genome	6 crisprs	cas3,DEDDh,cas14j,WYL,c2c9_V-U4,csa3,cas4,cas2,cas1,cas6,cas5,cas7,cas8b8,Cas9_archaeal	1	3	0	0

1. NZ_CP014263

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP014263_1

• CRISPR_ID: NZ_CP014263_1
• CRISPR_location: 955707-955799
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP014263_1

Consensus_repeat	Method
GTAGGGACGCAACAGCAGAAGGC	CRISPRCasFinder

spacers of NZ_CP014263_1

>1.1|955730|47|NZ_CP014263|CRISPRCasFinder
GTCGGTAGAGATGTAGGGACGCAACAGCCGAAGGCATCGGTAGAGAT

CRISPR arrays and Neighbor proteins around NZ_CP014263_1

CRISPR arrays

The CRISPR arrays of NZ_CP014263_1

>merge|NZ_CP014263|1|955707-955799|CRISPRCasFinder
GTAGGGACGCAACAGCAGAAGGCGTCGGTAGAGATGTAGGGACGCAACAGCCGAAGGCATCGGTAGAGATGTAGGGACGCAACAGCCGAAGGC

>NZ_CP014263|1|1|955707-955799|CRISPRCasFinder
GTAGGGACGCAACAGCAGAAGGC	GTCGGTAGAGATGTAGGGACGCAACAGCCGAAGGCATCGGTAGAGAT
GTAGGGACGCAACAGCCGAAGGC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014263.1|WP_077130022.1|947504_948008_+|pyridoxamine-5'-phosphate-oxidase-family-protein	unknown	unknown	gnl|CDD|379804
NZ_CP014263.1|WP_077133786.1|946758_946971_+|hypothetical-protein	unknown	unknown	gnl|CDD|227213
NZ_CP014263.1|WP_077130025.1|949536_950076_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130033.1|959856_960483_+|ATP-binding-protein	unknown	unknown	gnl|CDD|377306
NZ_CP014263.1|WP_077130024.1|948845_949487_+|phosphoglycerate-mutase	unknown	unknown	gnl|CDD|274461
NZ_CP014263.1|WP_077130027.1|952805_953615_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187616
NZ_CP014263.1|WP_077130035.1|962963_964058_+|tetraacyldisaccharide-4'-kinase	unknown	unknown	gnl|CDD|376853
NZ_CP014263.1|WP_077130023.1|948092_948827_+|DUF3891-family-protein	unknown	unknown	gnl|CDD|379025
NZ_CP014263.1|WP_077130034.1|961798_962914_-|o-succinylbenzoate-synthase	unknown	unknown	gnl|CDD|239436
NZ_CP014263.1|WP_077133788.1|960548_961472_+|oxygen-dependent-coproporphyrinogen-oxidase	unknown	unknown	gnl|CDD|376494
NZ_CP014263.1|WP_077130029.1|955069_955684_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077133787.1|958646_959288_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130021.1|947000_947414_+|four-helix-bundle-copper-binding-protein	unknown	unknown	gnl|CDD|153434
NZ_CP014263.1|WP_077130028.1|953773_954787_+|hypothetical-protein	unknown	unknown	gnl|CDD|226304
NZ_CP014263.1|WP_077130032.1|958005_958638_-|thioredoxin-family-protein	unknown	unknown	gnl|CDD|379658
NZ_CP014263.1|WP_077130031.1|957504_957945_-|peptidylprolyl-isomerase	unknown	unknown	gnl|CDD|223976
NZ_CP014263.1|WP_077130036.1|964109_966179_+|putative-porin	unknown	unknown	gnl|CDD|379481
NZ_CP014263.1|WP_083732744.1|955879_956872_-|UV-DNA-damage-repair-endonuclease-UvsE	unknown	unknown	gnl|CDD|235029
NZ_CP014263.1|WP_077130026.1|950136_952779_-|glucosidase	unknown	unknown	gnl|CDD|367389
NZ_CP014263.1|WP_077130030.1|957065_957470_+|hypothetical-protein	unknown	unknown	unknown

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP014263.1|WP_077130022.1|947504_948008_+|pyridoxamine-5'-phosphate-oxidase-family-protein	gnl|CDD|379804	pfam16242, Pyrid_ox_like, Pyridoxamine 5'-phosphate oxidase like. This domain, approximately 140 residues in length, is mainly found in general stress proteins in various Xanthomonas species. It is composed of a six-stranded antiparallel beta-barrel flanked by five alpha-helices and can bind to FMN and FAD, suggesting that it may help the bacteria to react against the oxidative stress induced by the defense mechanisms of the plant.	9.49161e-64
NZ_CP014263.1|WP_077133786.1|946758_946971_+|hypothetical-protein	gnl|CDD|227213	COG4876, COG4876, Uncharacterized protein conserved in bacteria [Function unknown].	2.15865e-05
NZ_CP014263.1|WP_077130032.1|958005_958638_-|thioredoxin-family-protein	gnl|CDD|379658	pfam14595, Thioredoxin_9, Thioredoxin.	1.91926e-45
NZ_CP014263.1|WP_077130033.1|959856_960483_+|ATP-binding-protein	gnl|CDD|377306	pfam04326, AlbA_2, Putative DNA-binding domain. This family belongs to the AlbA clan of DNA-binding domains.	3.2663e-28
NZ_CP014263.1|WP_077130028.1|953773_954787_+|hypothetical-protein	gnl|CDD|226304	COG3781, COG3781, Predicted membrane protein [Function unknown].	3.33325e-41
NZ_CP014263.1|WP_077130027.1|952805_953615_-|SDR-family-oxidoreductase	gnl|CDD|187616	cd05358, GlcDH_SDR_c, glucose 1 dehydrogenase (GlcDH), classical (c) SDRs. GlcDH, is a tetrameric member of the SDR family, it catalyzes the NAD(P)-dependent oxidation of beta-D-glucose to D-glucono-delta-lactone. GlcDH has a typical NAD-binding site glycine-rich pattern as well as the canonical active site tetrad (YXXXK motif plus upstream Ser and Asn). SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRS are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes have a 3-glycine N-terminal NAD(P)(H)-binding pattern (typically, TGxxxGxG in classical SDRs and TGxxGxxG in extended SDRs), while substrate binding is in the C-terminal region. A critical catalytic Tyr residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering), is often found in a conserved YXXXK pattern. In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) or additional Ser, contributing to the active site. Substrates for these enzymes include sugars, steroids, alcohols, and aromatic compounds. The standard reaction mechanism is a proton relay involving the conserved Tyr and Lys, as well as Asn (or Ser). Some SDR family members, including 17 beta-hydroxysteroid dehydrogenase contain an additional helix-turn-helix motif that is not generally found among SDRs.	2.80644e-135
NZ_CP014263.1|WP_077130035.1|962963_964058_+|tetraacyldisaccharide-4'-kinase	gnl|CDD|376853	pfam02606, LpxK, Tetraacyldisaccharide-1-P 4'-kinase. This family consists of tetraacyldisaccharide-1-P 4'-kinase also known as Lipid-A 4'-kinase or Lipid A biosynthesis protein LpxK, EC:2.7.1.130. This enzyme catalyzes the reaction: ATP + 2,3-bis(3-hydroxytetradecanoyl)-D -glucosaminyl-(beta-D-1,6)-2,3-bis(3-hydroxytetradecanoyl)-D-glu cosam inyl beta-phosphate <=> ADP + 2,3,2',3'-tetrakis(3-hydroxytetradecanoyl)-D- glucosaminyl-1,6-beta-D-glucosamine 1,4'-bisphosphate. This enzyme is involved in the synthesis of lipid A portion of the bacterial lipopolysaccharide layer (LPS). The family contains a P-loop motif at the N-terminus.	1.3227e-86
NZ_CP014263.1|WP_077130023.1|948092_948827_+|DUF3891-family-protein	gnl|CDD|379025	pfam13030, DUF3891, Protein of unknown function (DUF3891). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and archaea. Proteins in this family are approximately 250 amino acids in length.	3.71685e-86
NZ_CP014263.1|WP_077130034.1|961798_962914_-|o-succinylbenzoate-synthase	gnl|CDD|239436	cd03320, OSBS, o-Succinylbenzoate synthase (OSBS) catalyzes the conversion of 2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate (SHCHC) to 4-(2'-carboxyphenyl)-4-oxobutyrate (o-succinylbenzoate or OSB), a reaction in the menaquinone biosynthetic pathway. Menaquinone is an essential cofactor for anaerobic growth in eubacteria and some archaea. OSBS belongs to the enolase superfamily of enzymes, characterized by the presence of an enolate anion intermediate which is generated by abstraction of the alpha-proton of the carboxylate substrate by an active site residue and is stabilized by coordination to the essential Mg2+ ion.	1.61799e-76
NZ_CP014263.1|WP_077133788.1|960548_961472_+|oxygen-dependent-coproporphyrinogen-oxidase	gnl|CDD|376494	pfam01218, Coprogen_oxidas, Coproporphyrinogen III oxidase.	0
NZ_CP014263.1|WP_077130021.1|947000_947414_+|four-helix-bundle-copper-binding-protein	gnl|CDD|153434	cd08026, DUF326, Cysteine-rich 4 helical bundle widely conserved in bacteria. This functionally uncharacterized protein forms a 4-helical bundle with a bromodomain-like topology. It is present in major bacterial lineages and contains highly conserved cysteines in a repeated pattern, whose sidechains appear buried. Some family members have been (mis)annotated as putative ferredoxins.	3.45161e-21
NZ_CP014263.1|WP_077130024.1|948845_949487_+|phosphoglycerate-mutase	gnl|CDD|274461	TIGR03162, Adenosylcobalamin/alpha-ribazole_phosphatase, alpha-ribazole phosphatase. Members of this protein family include the known CobC protein of Salmonella and Eschichia coli species, and homologous proteins found in cobalamin biosynthesis regions in other bacteria. This protein is alpha-ribazole phosphatase (EC 3.1.3.73) and, like many phosphatases, can be closely related in sequence to other phosphatases with different functions. Close homologs excluded from this model include proteins with duplications, so this model is built in -g mode to suppress hits to those proteins. [Biosynthesis of cofactors, prosthetic groups, and carriers, Heme, porphyrin, and cobalamin].	3.39918e-54
NZ_CP014263.1|WP_077130031.1|957504_957945_-|peptidylprolyl-isomerase	gnl|CDD|223976	COG1047, SlpA, FKBP-type peptidyl-prolyl cis-trans isomerases 2 [Posttranslational modification, protein turnover, chaperones].	2.58509e-41
NZ_CP014263.1|WP_077130036.1|964109_966179_+|putative-porin	gnl|CDD|379481	pfam14121, Porin_10, Putative porin. This family of membrane bet-barrel proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 655 and 722 amino acids in length. SRI_1264 is identified by Gene3D as a membrane bound beta-barrel. These sequences are putative porins.	7.20414e-129
NZ_CP014263.1|WP_083732744.1|955879_956872_-|UV-DNA-damage-repair-endonuclease-UvsE	gnl|CDD|235029	PRK02308, uvsE, putative UV damage endonuclease; Provisional.	7.29796e-106
NZ_CP014263.1|WP_077130026.1|950136_952779_-|glucosidase	gnl|CDD|367389	pfam03200, Glyco_hydro_63, Glycosyl hydrolase family 63 C-terminal domain. This is a family of eukaryotic enzymes belonging to glycosyl hydrolase family 63. They catalyze the specific cleavage of the non-reducing terminal glucose residue from Glc(3)Man(9)GlcNAc(2). Mannosyl oligosaccharide glucosidase EC:3.2.1.106 is the first enzyme in the N-linked oligosaccharide processing pathway. This family represents the C-terminal catalytic domain.	3.17999e-11

Protein sequences

>NZ_CP014263.1|WP_077130029.1|955069_955684_+|hypothetical-protein
MKQFRLSIAVLLAVWGLAGMGDANADNGSGANGVKIEKSENKKVRLYIPNAPSKTAVDVAVIDAEGNVLYKGIVAHNKAGRQLFNLANLPDGQYFITATSDAWWMSQGITVKGNALSVDARNLQQVSKPTVVAYEKNKVEVTLPASNLSGAHVTIYDAQSTAVYSDKFAGTTRRFDLSSLPDGAYTVVVGPDQKQFSTPLTIRH
>NZ_CP014263.1|WP_077130028.1|953773_954787_+|hypothetical-protein
MFTTKRVPFYIVFPFAARSILFFLLYSTGICLLYWGLDWKFLAIPFVPIATIGTAVAFYVGFKNNSSYDRLWEARRIWGSLTNASRSWSIMVLDYIGPDQLADPVNEAELKRLHKELIYRHLAYLTALRVQLRQKPVWVQHRDPAHEVIERITEFKQCSLDKEVSRFISEHEAELLIRHPNPATYLLRQQSAQLRELRNEGYLSEYYHVDLERMLVEFYNQQGACERIKSFPFPRQYAFFSYVFTWLFIFVLPYGLLSEMAKASSWHIWLMVPFYTIIAWVFNTMEVVGDTSENPFENSINDVPMTAICRNIEIDLRDMLGETDLPKRVQAVNNILM
>NZ_CP014263.1|WP_077130027.1|952805_953615_-|SDR-family-oxidoreductase
MDQTLKGQIALITGASSGIGAGVAKSLAKAGATVVINYPVASSQVAAEAVLQEITDAGGQGMTAQCDVSQEAQVEAMFSDVVSRYGTVDILVNNAGIERNAPFHEQTLDQWNAVINVNLTGQFLCARAAIREFLRRGPRPEVSAATGKIICMSSVHELIPWAGHVNYAASKGGVKLMMQSLAQEYGDRRIRVNSICPGAIQTPINRPAWETPQAMSSLLGLIPYNRIGQPEDIGNLAVFLASDLSDYITGASIFIDGGMTVFESFATGG
>NZ_CP014263.1|WP_077130026.1|950136_952779_-|glucosidase
MTKPSAERLRVEEAAKKTIPLAKWGPYLSERQWGTVREDYSANGDAWNFFPHDHARSRVYRWGEDGLGGISDRRQNVCFALALWNHRDGILKERLFGLTNNEGNHGEDVKELYYYLDNTPTHSYMRMRYKYPQAPFPYGWLVHENGIRNRQEPEFEILHTGVFEEGRYFDVDVEYARKSDNDVCIRITVVNQGLDPAPLTVLPTLWCRNRWAFEPNVEKPTINRRPDAPHTGLAQLSHPKTGQYFLYYEPTDTALLTENETNMKRLYGVPNTSPFVKDAFHEAICQDDDYLLQLLQENQSGTKFAPVYALTLQPGESQSVCLRLVNELILKPFGEEFQQVFTDRVREADDFYRQLAPADTTTDRLQIMRQALAGMLWTKQYYHYDIPRWLQGDPGHLPPPPERVLGRNARWEHLNNEDVLSMPDKWEYPWYAAWDLAFHTVPLAMVDPAFAKNQLILLMREWYMNPQGQMPAYEWNFSDVNPPVHAWGALSVYKIEKAIYGNADIQFLKRAFQKLLINFTWWANRHDDEENNIFGGGFLGLDNIGVINRSHLPPGTLLEQADATAWMGMYALNLMDMALEITRYDPTFEDVATKFYEHFVLIGESLNQALWDEKDQFFYDLLHPMRGPSAKLEVRSAVGLSVLFAVSVIRREKCEPLADFLKRMSFFQRYHLELGRPMPEQLVNEQGDILLSLISRDKLEKLLQVMLDESEFLSPGGIRALSKYHEQHPYSVQINGDTYSIAYVPGDSDSGMFGGNSNWRGPVWMPINYLLIKSLKKYYQFYGDSLQVEYPTGSGNWLNLKQVSQALADRLVSIFEQDANGHRPVNGPFSPFYQRSENKELILFFEYFHGDTAQGIGASHQTGWTGAVAELINEDSWEWD
>NZ_CP014263.1|WP_077130025.1|949536_950076_+|hypothetical-protein
MKSISIRPATLMLMILAAALFRLLPHWPNFTPIAAMALFGAATFERKWLGLATPLAAMLLSDALIGFHGSMGAVYLSFGLTWLLGIWALQRPTAGRVASASVTASVLFFLITNFAVWYGSAFYPQTLAGLASCYVAGLAFYNGTSFFLNGLLGDLFFSGVLFGSFYLLQQRFPVLRVAQ
>NZ_CP014263.1|WP_077130024.1|948845_949487_+|phosphoglycerate-mutase
MDVYLIRHTEVAVGRSVAYGQSDVDLADAYDEQRDRLLAHLPTDAAAIFSSPLTRCRRLADDIAGSMAAGSRIETAPGQTALIDAHRPVVVHDDRLKEYHFGDWEMVPWATIDRAALDPWMADFVTVRVPNGENFQDLFDRVSRFWREQILPLAETQPGQPVFIVTHGGVIRALLCLFLDLSLHNAYRINLDYGAVTKLTLTDLSYTIQYINR
>NZ_CP014263.1|WP_077130023.1|948092_948827_+|DUF3891-family-protein
MIVIQTDTGWQVIHQQAHGLLAVQAAMHWQVDKRPKYWIETLIALTEHDDGQDPWEGRNHLTTAGAPLHFQVLEYSVEQCRNMIAISLDKSRWNALMLSMHTSFLYEEKRGTDKALDEFLDQQIDNQKKWRKQYAATKADAQYAYDFIQWCDALSLILCLNQVPPEGRRLEISKGPDGVSYYILQNPNGSLCIDPWPFDVPAFAAHVEVFELNQLVFSDDNELYNALQDAPLALKEWQFVQRSQ
>NZ_CP014263.1|WP_077130022.1|947504_948008_+|pyridoxamine-5'-phosphate-oxidase-family-protein
METKPQKNEKLEKVRKMVGDIRIAMMTTVNDEGQLMSRPMAALEMDEDATIWFFTQKTSPKVAQIEQHERQVNLAFVNVSDADYVSISGTADEIDDRAKIDELWNPQAKAWFPNGKDDPNLTLLRVHTHMAEYWDSNDSTMVRLFQQASAALTGTVPKMGENEKVYN
>NZ_CP014263.1|WP_077130021.1|947000_947414_+|four-helix-bundle-copper-binding-protein
MIWNKTIYDTLTSCATLCDEFATECSRSEDIENWYRSIFLNLDCADMCRQLAMLYVRGSENTRLLATACIEVCEKCAQEIAQFDTERCQQVYAMCQQTILSCVSILNMQRNDADAKNPTSTPASLFYGIDLRETIYN
>NZ_CP014263.1|WP_077133786.1|946758_946971_+|hypothetical-protein
MWTPTHFPAAMRSLNPSTRAKAIEIANQLLEQGQLDKQRAITISIIEARRLARMYAVETDRIGRSVSSYA
>NZ_CP014263.1|WP_083732744.1|955879_956872_-|UV-DNA-damage-repair-endonuclease-UvsE
MIVSPLNVGYACINLTLQAEKILTNRGMIKKTFAERGIQYASQLALKNVQDLLTIVDWNLAHGFGLFRISSDIFPWASEYRLANLPDFTEIRTLLEEIGSRPIRLTTHPGPFNHLAGQGNVLKNTLVDLEYQSEIFDLMGLKPSHWNKINIHLGGTYGDKPGTIARFCQNFGLLSENLRARLTVENDDRVSLYTVADLVPVYEAIGTPVVFDYFHHALNPGTLTEEEAFLMAYGTWDVRPVFHYSDSRQEREDPKARREAHADWLYSIANTYGKEVDIVFESKMKELAILRLRGNEPVITPKLAKLINQAKKQDPENPPAEAVETSDVAL
>NZ_CP014263.1|WP_077130030.1|957065_957470_+|hypothetical-protein
MEDLTTDQIIGIATGYRNMARALNEFQVRRWPEFTHEQQLDVNAYQNSLLNRAHDLQSLLVRPAFKYPLDIATDIVQATDTARNSLKIIRNLTVALNVGAIMVALASYVARANLRGIQTALRELRELVMLEEEK
>NZ_CP014263.1|WP_077130031.1|957504_957945_-|peptidylprolyl-isomerase
MAQAKAGDTVQVHYTGTLTDGTVFDSSAGRTPLEFIVGSGQVIKGFDEGVEGMNTGEKKTINIPVEDAYGSANEEMIFTLNRSDIPDDIPLEVGMTLNMHEDGNPRPIPVIVRQLSDSSVTLDANHPLAGQNLVFEVELVGVKTNE
>NZ_CP014263.1|WP_077130032.1|958005_958638_-|thioredoxin-family-protein
MSIDSPVITPDLIASAMTYDQYVALSTERFNEGRSTTIDPHYNTPEILGYVKLNLHRMSRLHRLTTLEPELRKALAEVLEPWTWLVLTESWCGDAAQSLPVIDLMASESPSITVGYLLRDENPALMNAYLTNGGRSIPKLICLRTRDLSEIGTWGPRPAGLQNLMIDWRTEKLPLSEAVERAQRWYNDDHTQSVQAELLTLVRGWSKISV
>NZ_CP014263.1|WP_077133787.1|958646_959288_-|hypothetical-protein
MTLTPFETKLYHQLTPFFARHQYVLLSEKKQFRRTTETGFQNVILSPAFYSDETMLEVNFGCRSDQVEQIAQQFLNNLPDYRPDANTLILSIGKFNGFQYFRYKIHSDDELSDVCGQIEQFFDLEGFEFLDTACTLHNLDRLLNDQPNQPSRYVYNQTHRCYKGLIAARLNHNPHFDGLVDSYRHLMIRQTQNAYEQLHFERLITYLQHYSAN
>NZ_CP014263.1|WP_077130033.1|959856_960483_+|ATP-binding-protein
MTFTELIALIEQGESNRLEFKRTLSSAHRIARTLAAFANTAGGTLLIGVADDGRITGVSSELREMRKIEEATDQLINPPLTVSYQTIAPDGRNVLIINVPESDEKPHTAISEAGKHTIYVRARDKSVPTNQLIINPEPADAQLLKSPTARTLIQYLRKNDHITADKFAKLINVSEYRATKLLRQFAGQGLLLLIDNQRAGRYALKLTE
>NZ_CP014263.1|WP_077133788.1|960548_961472_+|oxygen-dependent-coproporphyrinogen-oxidase
MVTEQRISKETIATFFMDLQDRICRSLEDADGGATFREDAWQRPGGGGGRSRIITDGAVIEKGGVGFSAVHGEATEATLRSLNLTEPAEFYATGVSIVLHPRNPMVPIIHMNVRYFEVSTATFVGGHNWFGGGIDLTPHYVDEDDARWFHTYLKTVCDRHAVADYSRFKTWADDYFYIPHRQETRGIGGIFFDYLKPTDDVDKADLFAFVQDVGNAFAPIYTHFMHQNRELPFGEREKQWQLLRRGRYVEFNLVWDRGTKFGLETNGRTESILMSMPPQANWIYDHHPEANTREAETLGWLRKGIDW
>NZ_CP014263.1|WP_077130034.1|961798_962914_-|o-succinylbenzoate-synthase
MSLRADYLKYTLHFRFEAGTSRGTLTEKTSYLIRLFDDEDSSTIGYGECGPLKGLSYDDRPDFEEQLREYCREFTSLDLQLFSWNVPIVLNQLIDPKFPSILFGFETAMLDFLSGGRHIVHETEFTTGQRSLPINGLIWMGSAATMRQQIEEKIKAGFTTLKLKIGAIDFEQECDLLAMIRDRFSPEQITLRVDANGAFRPNEAMAKLERLATYGLHSIEQPIRAGQPEQMAELCRHSPLPIALDEELIGQMEYVHKYKLLKSIHPQYIILKPTLLGGMRHCDEWIELAGRLNIGWWITSALESNIGLNAIAQYTAQFKNLMPQGLGTGQLYYNNFDSPLTIREGYLHYHPGQPWDFSALQKSSIRSSVDK
>NZ_CP014263.1|WP_077130035.1|962963_964058_+|tetraacyldisaccharide-4'-kinase
MLEKGNITKLLAIRFVRKWLLLPVSWLYGWVMNVRNILFDKGLFVSLMPDVPTICVGNLTVGGTGKTPAVEYLIKWYVRNEPGVPLETVTLSRGYGRRTKGFRITTESDTADTVGDEPLQLYRKFGHLVRVCVGERRADAIQFILRQFPETERILLDDAFQHRAVRSHLNVLLMDYNRPFYDDYPFPAGRLRESRHGASRANVIIVTKCPDNLNATERTAIEAHIRPYARPETPVFFAGLHYEQPVSFATHQSANGLTNVVLVSGLANADPLERYVSQVFKLVRHHRFADHYAYSRTNLNALLASLPTDAALLTTEKDWVKIDVLLTPNERATLPLYYLPVAMRFLEGEERFSALLTQDALKKS
>NZ_CP014263.1|WP_077130036.1|964109_966179_+|putative-porin
MNQRFLFLLLFSIAALSGRAQQFPGTTQPGQFPGGFGNQQGRPTGSGNSQSSSSGGIDDSTKVIYGPKSTRYILEDDVLNNRQKQYLVDTTMDDVHRYLYVHRTQNQYQDLGNLGTPMRPVFVQVPDQLGSQTGYSVFSEYAYNPMNVKYFNTRSPFTDMYVALGGRNQNILRFDFAQNITPRWNVGFALQRFTSNRQFGAQGQTSQLNRQLAENWGFLGHTNYQSKNNKYTLLMNFINMNHSLGEQGGLIPGQFLDGSINRFAYTGDARLSSGVVQTGFAPAVPGPRGNEIRNNWHVYQQYVLDKGFQIYDRLEYQRQKNSYRDDTLRFNQEPRQVTDNLVLPGFYPSRRNDPNLTTLGDTSRILVDARFRVLDNQFGVKGIYQLGKSAFNYRAYLRNRLLGQYTLYNTGRAVENEYETRRLETFVGGWLGYYFPDSLSRLTAELEYQLGGGFRLKGQLESKWFTAGYTAMLVQPTLLQERFESIVFNWRNSGLRGFNHAYGRLNLRYKGIRLEPGLDYHLLSNYIYFDTNAVARQDNGSFSVLRTGLGYQYQRGRFLLAGQAYYTLQSRDDVLRTPPFFWNGRFQYELIYAKVLYIQVGVDLHYKSPYFADAYMPVTQQFHLQNRQRVEGYVLADLYANLRVNRTRLFVKLTHANQGVLQGPGYFVAPDFLQMRRGFAFGVDWYLFD

Crispr_ID: NZ_CP014263_2

• CRISPR_ID: NZ_CP014263_2
• CRISPR_location: 2034878-2034961
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP014263_2

Consensus_repeat	Method
AGAGACGGAACATCTTCCGTCTC	CRISPRCasFinder

spacers of NZ_CP014263_2

>2.1|2034901|38|NZ_CP014263|CRISPRCasFinder
CCTCGCGTCAGCCATACATTAAAAAAACCATCCGGCGG

CRISPR arrays and Neighbor proteins around NZ_CP014263_2

CRISPR arrays

The CRISPR arrays of NZ_CP014263_2

>merge|NZ_CP014263|2|2034878-2034961|CRISPRCasFinder
AGAGACGGAACATCTTCCGTCTCCCTCGCGTCAGCCATACATTAAAAAAACCATCCGGCGGGGAGACGGAACATCTTCCGTCTC

>NZ_CP014263|2|2|2034878-2034961|CRISPRCasFinder
AGAGACGGAACATCTTCCGTCTC	CCTCGCGTCAGCCATACATTAAAAAAACCATCCGGCGG
GGAGACGGAACATCTTCCGTCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014263.1|WP_077130844.1|2024288_2024804_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130851.1|2029958_2032355_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|274576
NZ_CP014263.1|WP_077130850.1|2028832_2029732_+|DUF2911-domain-containing-protein	unknown	unknown	gnl|CDD|378565
NZ_CP014263.1|WP_077130843.1|2022817_2024035_+|ADP-forming-succinate--CoA-ligase-subunit-beta	unknown	unknown	gnl|CDD|234813
NZ_CP014263.1|WP_077130861.1|2049989_2051564_-|acyl-CoA-carboxylase-subunit-beta	unknown	unknown	gnl|CDD|130187
NZ_CP014263.1|WP_157579179.1|2048808_2049642_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_083732799.1|2037869_2040554_+|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP014263.1|WP_077130855.1|2040669_2042199_+|gliding-motility-associated-C-terminal-domain-containing-protein	unknown	unknown	gnl|CDD|372639
NZ_CP014263.1|WP_077130856.1|2042224_2044255_-|hypothetical-protein	unknown	unknown	gnl|CDD|369609
NZ_CP014263.1|WP_077130842.1|2022020_2022677_-|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213222
NZ_CP014263.1|WP_077130848.1|2027752_2028139_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130859.1|2047461_2048739_+|aspartate-aminotransferase-family-protein	unknown	unknown	gnl|CDD|99735
NZ_CP014263.1|WP_077130853.1|2034983_2037386_+|FtsX-like-permease-family-protein	unknown	unknown	gnl|CDD|274576
NZ_CP014263.1|WP_077130845.1|2025014_2026097_+|hypothetical-protein	unknown	unknown	gnl|CDD|366675
NZ_CP014263.1|WP_077130852.1|2032480_2034874_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|274576
NZ_CP014263.1|WP_077130854.1|2037534_2037873_+|PadR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|367559
NZ_CP014263.1|WP_077130849.1|2028219_2028762_-|NUDIX-hydrolase	unknown	unknown	gnl|CDD|239646
NZ_CP014263.1|WP_077130858.1|2046199_2047420_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130847.1|2026864_2027629_-|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|235546
NZ_CP014263.1|WP_077130857.1|2044328_2046020_-|sodium:solute-symporter	unknown	unknown	gnl|CDD|271385

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP014263.1|WP_077130854.1|2037534_2037873_+|PadR-family-transcriptional-regulator	gnl|CDD|367559	pfam03551, PadR, Transcriptional regulator PadR-like family. Members of this family are transcriptional regulators that appear to be related to the pfam01047 family. This family includes PadR, a protein that is involved in negative regulation of phenolic acid metabolism.	3.43107e-05
NZ_CP014263.1|WP_077130851.1|2029958_2032355_+|ABC-transporter-permease	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	1.79623e-90
NZ_CP014263.1|WP_077130850.1|2028832_2029732_+|DUF2911-domain-containing-protein	gnl|CDD|378565	pfam11138, DUF2911, Protein of unknown function (DUF2911). This bacterial family of proteins has no known function.	2.27234e-65
NZ_CP014263.1|WP_077130843.1|2022817_2024035_+|ADP-forming-succinate--CoA-ligase-subunit-beta	gnl|CDD|234813	PRK00696, sucC, ADP-forming succinate--CoA ligase subunit beta.	0
NZ_CP014263.1|WP_077130861.1|2049989_2051564_-|acyl-CoA-carboxylase-subunit-beta	gnl|CDD|130187	TIGR01117, methylmalonyl-CoA_decarboxylase_alpha-subunit, methylmalonyl-CoA decarboxylase alpha subunit. This model describes methymalonyl-CoA decarboxylase aplha subunit in archaea and bacteria. Metylmalonyl-CoA decarboxylase Na+ pump is a representative of a class of Na+ transport decarboxylases that couples the energy derived by decarboxylation of carboxylic acid substrates to drive the extrusion of Na+ ion across the membrane. [Energy metabolism, ATP-proton motive force interconversion, Energy metabolism, Fermentation, Transport and binding proteins, Cations and iron carrying compounds].	0
NZ_CP014263.1|WP_083732799.1|2037869_2040554_+|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	2.95754e-66
NZ_CP014263.1|WP_077130855.1|2040669_2042199_+|gliding-motility-associated-C-terminal-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.	1.66772e-15
NZ_CP014263.1|WP_077130856.1|2042224_2044255_-|hypothetical-protein	gnl|CDD|369609	pfam07944, Glyco_hydro_127, Beta-L-arabinofuranosidase, GH127. One member of this family, from Bidobacterium longicum, UniProtKB:E8MGH8, has been characterized as an unusual beta-L-arabinofuranosidase enzyme, EC:3.2.1.185. It rleases l-arabinose from the l-arabinofuranose (Araf)-beta1,2-Araf disaccharide and also transglycosylates 1-alkanols with retention of the anomeric configuration. Terminal beta-l-arabinofuranosyl residues have been found in arabinogalactan proteins from a mumber of different plantt species. beta-l-Arabinofuranosyl linkages with 1-4 arabinofuranosides are also found in the sugar chains of extensin and solanaceous lectins, hydroxyproline (Hyp)2-rich glycoproteins that are widely observed in plant cell wall fractions. The critical residue for catalytic activity is Glu-338, in a ET/SCAS sequence context.	4.2958e-57
NZ_CP014263.1|WP_077130842.1|2022020_2022677_-|ABC-transporter-ATP-binding-protein	gnl|CDD|213222	cd03255, ABC_MJ0796_LolCDE_FtsE, ATP-binding cassette domain of the transporters involved in export of lipoprotein and macrolide, and cell division protein. This family is comprised of MJ0796 ATP-binding cassette, macrolide-specific ABC-type efflux carrier (MacAB), and proteins involved in cell division (FtsE), and release of lipoproteins from the cytoplasmic membrane (LolCDE). They are clustered together phylogenetically. MacAB is an exporter that confers resistance to macrolides, while the LolCDE system is not a transporter at all. An FtsE null mutants showed filamentous growth and appeared viable on high salt medium only, indicating a role for FtsE in cell division and/or salt transport. The LolCDE complex catalyzes the release of lipoproteins from the cytoplasmic membrane prior to their targeting to the outer membrane.	3.18616e-104
NZ_CP014263.1|WP_077130853.1|2034983_2037386_+|FtsX-like-permease-family-protein	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	5.47153e-51
NZ_CP014263.1|WP_077130845.1|2025014_2026097_+|hypothetical-protein	gnl|CDD|366675	pfam01494, FAD_binding_3, FAD binding domain. This domain is involved in FAD binding in a number of enzymes.	2.39846e-35
NZ_CP014263.1|WP_077130852.1|2032480_2034874_+|ABC-transporter-permease	gnl|CDD|274576	TIGR03434, ADOP, Acidobacterial duplicated orphan permease. Members of this protein family are found, so far, only in three species of Acidobacteria, namely Acidobacteria bacterium Ellin345, Acidobacterium capsulatum ATCC 51196, and Solibacter usitatus Ellin6076, where they form large paralogous families. Each protein contains two copies of a domain called the efflux ABC transporter permease protein (pfam02687). However, unlike other members of that family (including LolC, FtsX, and MacB), genes for these proteins are essentially never found fused or adjacent to ABC transporter ATP-binding protein (pfam00005) genes. We name this family ADOP, for Acidobacterial Duplicated Orphan Permease, to reflect the restricted lineage, internal duplication, lack of associated ATP-binding cassette proteins, and permease homology. The function is unknown.	1.01696e-69
NZ_CP014263.1|WP_077130849.1|2028219_2028762_-|NUDIX-hydrolase	gnl|CDD|239646	cd03674, Nudix_Hydrolase_1, Members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity. They also contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, U=I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	1.50974e-41
NZ_CP014263.1|WP_077130859.1|2047461_2048739_+|aspartate-aminotransferase-family-protein	gnl|CDD|99735	cd00610, OAT_like, Acetyl ornithine aminotransferase family. This family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). The major groups in this CD correspond to ornithine aminotransferase, acetylornithine aminotransferase, alanine-glyoxylate aminotransferase, dialkylglycine decarboxylase, 4-aminobutyrate aminotransferase, beta-alanine-pyruvate aminotransferase, adenosylmethionine-8-amino-7-oxononanoate aminotransferase, and glutamate-1-semialdehyde 2,1-aminomutase. All the enzymes belonging to this family act on basic amino acids and their derivatives are involved in transamination or decarboxylation.	5.01059e-133
NZ_CP014263.1|WP_077130847.1|2026864_2027629_-|SDR-family-oxidoreductase	gnl|CDD|235546	PRK05653, fabG, 3-oxoacyl-ACP reductase FabG.	2.37348e-75
NZ_CP014263.1|WP_077130857.1|2044328_2046020_-|sodium:solute-symporter	gnl|CDD|271385	cd11494, SLC5sbd_NIS-like_u2, uncharacterized subgroup of the Na(+)/iodide (NIS) cotransporter subfamily; putative solute-binding domain. Proteins belonging to the same subfamily as this uncharacterized subgroup include i) NIS, which transports I-, and other anions including ClO4-, SCN-, and Br-, ii) SMVT, which transports biotin, pantothenic acid and lipoate, and iii) the Na(+)/monocarboxylate cotransporters, SMCT1 and 2. SMCT1 is a high-affinity transporter while SMCT2 is a low-affinity transporter. This subgroup belongs to the solute carrier 5 (SLC5) transporter family.	3.03478e-162

Protein sequences

>NZ_CP014263.1|WP_077130852.1|2032480_2034874_+|ABC-transporter-permease
MFRNYFKIAFRSLWKNRVYSGINVVGLAVGLAACLLITLYVADELSYDRYHKRADRIYRVVHRATWEGGSMNLAPTSAPYAPTLKQTYPEIEQAVRILPEGGGIIQYGTTKVEAEDIAFADQNLFQVFSYSFLHGDPNMALSKPHSIVLTQTLAARLFGDVASAMSKTVLFENNFPNVVTGIISDMPANSHARFSALRSFSTGFTSGWQQFNLHTYLLLQEGADPKKVEAKFPAFFERYIKPEVGNVAYEMSLQPLTFIHLRSNLDYELSPNGSYRTVSVFAIIAGLILLLAGINYINLATARSSIRLREVGVRKAVGSGRGQLAGLFLIETSLLTVLATTLGVGLAYALMPFFNQLTGKELSMWRFGTGYSMLILVGFAVITSLLSGTYPALFLSGSRTVAALRGQMGSQLATIMFRKSLVTFQFAITVALIAASGIIYQQLQFAMNKSLGFNKDQVLTFHLHDDETRTKIPVLKAKLLQSPLIEDVAVASNPIGTNNLGGGGYYFEIDGKMTTSSKIIHSIMVDGDFLKTMEIGLVEGRSFSNTIPADRYNAILVNETLVKELGWKDPIGKRVKFYVDDKGTQAERRVVGIVKDFHTHSLQHKIEPLALQMPPSADEQDNVYIRIRAGQTEAALAFIQKTYEQFEPGGVFDYQFLDQNFARQYTNEQNQNNLLLIFTALAIFIACLGLFGLVTFTAEQRTKEIGVRKVLGASVISIVALLSKEFLKLVLIAIMIASPLAWYAMNRWLQGFAYKIDISWWMFVLAGLLAVGIALLTVSFQSIKAALMNPVKSLRSE
>NZ_CP014263.1|WP_077130851.1|2029958_2032355_+|ABC-transporter-permease
MLQNYLKIAVRNLWRNPLYSLLNLGGLALSTACCLLIALYVYDEWSYDRHYRDASRIFRVVERQQQPDGVYDVAATPGPLAPSLKATMPDVVEAGRIGRWNGLLRYGRQVYEEKSLFFADNGLLQLFNFPFLKGNPATALTRPDELVLTETAARRYFGANWQQNPKVIGATLRLNNERDYRVVGVLRDLPTNTHLRFDVLLSFKNVELDKSSYSWDWNSYHTYVRMRPNWSGDRADFGQKLTALYVRNNPTSKNTLSPQPLTDIHLYSDFAFNTDWGQRGSIFYVRLFATVGLIVLLIACVNFINLATARSMQRAREVGVRKTIGAHRRHLIFQFLGESFLLTGIAVGLALLLASGLMPLFNDLTGKTLTLDVSRLSFWVALVLLTGLIGLLAGAYPAFLLSSFQPATVLKGAITVRAGVTFRQVLVVGQFALSLILIISSVLIYRQLVYIQQKDLGFDKSQLLYARMAGALRFKAAEFKQELLRQSGIESAAATTATLVDVANESDIEWEGRQGRIERVRTDFFITQMNIDPDFTKTVGMKVARGSNFRPKAATDTNQTYLINETAARRMGYTVESAIGKRVKFWGKVGPIVGVVRDFHFRPLNVPIQPFIFRYAPDNPYFQLLVKTRPGQTATVLRHIEQLYKQYEKESPLHYGFVDQELDQQYQREQRTGRIVLYFSGLAVLISCLGLFGLAAFTAEQRTKEIGIRKVLGASVASIVALLSKDFLKLVGVSILIASPLAWYAMNRWLADFAYRIDIEWWVFALAGVLAVGIALLTVSFQSIKAALMNPVKSLRSE
>NZ_CP014263.1|WP_077130850.1|2028832_2029732_+|DUF2911-domain-containing-protein
MRKLVLSGVTLCLVAQLATAQIKLPSPSPAATIMQTVGTTDLTVKYSRPSLKGRTPFTDAFVPLGKVWRTGANQATAFTTTTDLMVNGKTLPAGTYAIMSIPTENDWTLIFNKNTSVSEQSYKQEEDALRVSIQPTETNEKAETFTIGFGDLTDSTATMSFMWANYKATANLAVNTAANAAANVDKAVAEKPDDAAVLQAAASYNLSKGRNLEQSLGMIDKAIAAKETFRNLFVKAQLLGKMGKFTEALPVAQKALSLGQTSNDAAFPFFKDGIEKSIAEYTSKLPAMPALKGKKGKKA
>NZ_CP014263.1|WP_077130849.1|2028219_2028762_-|NUDIX-hydrolase
MHRLPLLTLLRQHTPADTHERAMTEATIAFVEKHPDCFERSLLIGHVTGSAFIVSPDYAQMLLIHHRKLDRWLQPGGHADGDPDVAAVALREAQEETGLTQLQFASQQIFDVDVHTIPARGDVPEHLHYDVRFLFVSNTREKFGFSTEIKNIRWFSLDEADFYTNDSAFSRIRSKIYAKL
>NZ_CP014263.1|WP_077130848.1|2027752_2028139_-|hypothetical-protein
MKKSIFTLAVLCLLALTSCTMAQDNKRNDHTYSTANYKHANKAATARQWEANKGVAVQQPKPGDASVANYKRQTPAQQPAGGVTVEHTPSTDVAERNYKMQRPAQSATNNAAIAGKRKGKMVETTIGD
>NZ_CP014263.1|WP_077130847.1|2026864_2027629_-|SDR-family-oxidoreductase
MNRFQGKRVIITGGSGGIGKTTAKLFLEEGATVLLVDLDEEKLQAVANELGDRAHYAKADVTKADEVEAYAKAAADKMGGVDIFFNNAGIEGIVKPLVDYPEDIFQKVLSVNVLGVWLGLKYVMPIMKQGGGGSVIITSSVAGLRGTPNVSAYVTSKHAVVGLMKVAALEGAADNIRVNTVHPSPVDNRMMRSLEEGFAPGGAAQAKEQFAKAIPLQRYAEETDVSKLVLFLASDDASFLTGGQFTVDGGQTAA
>NZ_CP014263.1|WP_077130845.1|2025014_2026097_+|hypothetical-protein
MDRDITIIGAGSTGLSAGLFLESLGYKPRIFEKRDRVKITKAIGINPVTLQLFEKYGLTKRFINNGWRLDCMNFWYNDDLIYKNQFSKVRHPYPFMVIQPQFETEQILEDYLSEKGIKIERNVELLKISNDRTSMNLEFKNINNDTNFSLQTDGIVIGADGNKSKVRQEIGVEMKGWEHPTEYTLYDIELETPISHKEGHYRFYRDGAMLMLHIRDGVWRVGGNLKDVLNYLPKDTKIGKTSWETNFTISEKVAQNYSVGNVHIIGDAAHIHSPLGGKGMNMCIEDSYIFSELFHQNREKEFSTIRRKRVQTTVGVLGQLTEVVGGQHFIGRVMRGSMKPFSFLFPVFMPYMRNFLLGLK
>NZ_CP014263.1|WP_077130844.1|2024288_2024804_+|hypothetical-protein
MANNPMLHLMVGKWKTPNHSNCKADDDSHKVKKKILKRIGRKNFSKKVGDNPDIDITVEGVIILKGRGKFKNRPYFVSDISADDYFVLKFVPFTESNEVEISILVPDKEEENNDTGFEFEFISDKLYIIPNDERLILITINYLIDKYINNNTKQEENFLVVLQSNNLKNED
>NZ_CP014263.1|WP_077130843.1|2022817_2024035_+|ADP-forming-succinate--CoA-ligase-subunit-beta
MNIHEYQGKDILKKYGVRIQEGIVAESPEKAVEAAKQIMAQTGSKFVVVKSQIHAGGRGKGKIVGSEQRGVALAKSVDDVRTIAINLIGNVLVTHQTGPEGKKVNKILVAQDVFYPGASEPKEMYLGILLDRSKACNVIMASTEGGMDIEEVAEKTPEKIVKEWIDPAVGLQPFQARKIAFGLGLEGEAFKEMVKFVTSLYKAYVDTDASMFEINPVLKTSDNKILAVDAKVNLDDNALYRHPDLANLRDLSEEDPLEVEASANDLNYVKLDGNVGCMVNGAGLAMATMDIIKLSGGEPANFLDVGGGANAKTVEAGFRIILKDPNVKAILINIFGGIVRCDRVATGVVEAYKAIGDIPVPIIVRLQGTNAEEGARIIDESGLKVQSAVLLKEAADKVRAVVEAM
>NZ_CP014263.1|WP_077130842.1|2022020_2022677_-|ABC-transporter-ATP-binding-protein
MPLLHASDLRRNYGNLSVLKGINLTIEPGEVVSIVGASGAGKTTLLHILGTLDRPDTGSLQIANQDVFILTDNQLARFRNERIGFVFQFNNLLPEFTALENVCLPGFIAGKDERTVRQRAESLLTTLGLRERLGNLPSQLSGGEQQRVAVARALINEPAIVFADEPSGNLDSRNAEELHQLFFRLRDELGQTFIIVTHNEALAALADRTVTIRDGVIE
>NZ_CP014263.1|WP_077130853.1|2034983_2037386_+|FtsX-like-permease-family-protein
MLRNYFKIAWRNLLRNKTYSFINIGGLAVGMAVAILIGLWIYDELSFNKYHQNYDRIAQVREHGIREDGKHYSNTSLPYPLATELKTSYQRFFKHILIANDPGEYILTTGETKLTQKGQFIEAGAPEMLTLTMLKGSWAGLTDPHSILLSASAATALFGDADPIDKPVKINADMEAKVTGVYLDLPHNSEFHPIKFFAPFDLWTSANPWVREQQWNNWFLSVYAQVQTNVDFDKVSAIIKDIEINQIKNLKDRQEQVARQPQIALLPMSRWHLYGSYYVDDNGPVQMVWLIGLIGAFVLLLACINFMNLSTARSVKRAQEVGIRKAVGSLRGQLMSQFFSESFLVVLLAFMLSLSLVGISLPWFNDIAAKQLTVPWTASPFWLACVLFVLATGFLAGSYPAFYLSSFQPVKVLKGVVIQGRFAALPRKLLIVLQFTVSVTLIIVTLLVYRQIQHAKNRPIGYDKAGLVMVEKKTADFNDKQQLLRSELKNTGVVVEVAESRSSPTGITMWNGGFSRKGIAFDCPNGCGTLPVSPEYGQTVGWQFVAGRDFSKALATDSLGFIINESFAKLLELKTPVGEQVTWGPGQRLPKTYTVLGVVKDMVALSPYKPTIPTVFFLEDNYNWINIRLNPAISASEALPKIEAVFKKIIPTAPFDYKFADQEYAAKFAAEERIGNLALVFTVLAVLISCLGLFGLASFMAEARTKEIGVRKVLGASVLNLWGLLSKDFVILVIISFFIATPIAYYFLSNWLQKYEYRTELSWWIFAVSGAGALVITLLTISFQSVKAALMNPVKSLRTE
>NZ_CP014263.1|WP_077130854.1|2037534_2037873_+|PadR-family-transcriptional-regulator
MKRTYLGEFEEIVLLLVVSMDGEAYGVGLTHKLNEETDRSVRLNQVHAALHRLQEKGMVASRLGDPTPERGGRRKLLFTVTAYGYRTLQDIKVMRAQLWNAVPTTPKLAIGL
>NZ_CP014263.1|WP_083732799.1|2037869_2040554_+|FtsX-like-permease-family-protein
MKPSPPRLADRLLEWFVAPHRLEALQGDLHEEFAYQVGRMGVRRARWQYWRDVLGFMRPWVVKRKANEYPNPTNTDMIQNHLKIAWRSILRHRSFTGLNVLGLSVGIAAALLLFMTVRYELSFDTFHPEHDRIYRVVREQFLTNGDRDVTPGNPLPVADALKTDVAQFENVVSVFGTLDPQVTVLGSDPKTTNATTKFLEDDEGMIVGPEFFRLFNFPWLIGRPDALTQPNVVALSKTFAEKYFGSPQQAMGKFLRINKHTTMRVVGVLADAPPNTSFPMNLVISYATKKADKGERFGFGSFDDWGSTSSQDQIFVRLPRNLPVASANALLEKFSRKHYDGRDESKKTHFLSPLADLHHDNRFDTFTTKVAVVPFQRIWNLALVGGLLLLMACVNFVNIASALATRRAKEVSVRKVLGSQKSQLVGQFLTETFLMVLASLMLGIGLAYVALPLLNTLFAIPADASLYFKPELGLALLGLLVLLTLLAGLYPALVLSSFSPLDVFRKRVARGWLRGISVRQSLIVFQFATALVLIISTVINLRQMNYLSRMDTGFSKEGVFNFGMDTEYRTRNATLRNELLRVPGVSAVTFSSDVPSSDSRWQSTFAFANLSKDEDFTASMKMADGNYFTTHGITFVAGASYAVGDTLPKFVANETLLKKLGVKNPASVIGRNLRLGDVTGPIVGVVKDFHTNSARDDGGPRTRGIQPLLLTPSDKFYYAGSVKIRSQNLPQTVERIKAVYARVFPEVAFTGRFYEDALNAYYKAEQQMGLLYRVFAGLTIFIACLGLFGLAAFTAEQRTKEIGVRKVLGASVAGIVALLSKDFLKLVLVAVLIASPIAWYLMNGWLQDFTYRINIDWWVFALAGLLAVSIALLTVSFQSVKAALMNPVKSLRSE
>NZ_CP014263.1|WP_077130855.1|2040669_2042199_+|gliding-motility-associated-C-terminal-domain-containing-protein
MRWSVGLIVCLSLWTSVRAFGQELIPNGGFETYATCPRKDNLLSEATPWYNPNTATPDFYHSCFPTPQMELPPHSGQGLARLFMDLGWAEYLATPLKEPLLAGETYQFELYVASPKPTQYPIGSFGAYFANQPVGSADKTLLRLDNPPQVLDNTPRRLTQRLKWEKMGGCLLAKGGERHVVIGNFAALPSTLGDYYLFIDDVSLKPIRLDLGRDTTLCGRRSTLLLDATTPGAIFYEWNTGSNAPTLQVAKPGRYWVTVQTPCKTLRDTITVTYPPDFSLGADTTLCEGKTLMLHVDAPGTYQWQDGSRRNTFLVERAGQYVVQVTNKNCMVADTIAVRYSRPPQLDLGADQQLCGTEVYTIRPTFANGTFRWLDAFADVERTVNASGIFRASVTNACATRTDDVLIDYSGCSCQVYAPDAFSPNTDGLNDVFEPFACNDITFLTLTVYDRWGEAVFHTDQPPFRWNGTYQGERCATAVYTWQLSYLFQRPDAPPIRQTKQKRLTLLSQ
>NZ_CP014263.1|WP_077130856.1|2042224_2044255_-|hypothetical-protein
MALSRSLRIFFVFSCFATLIATAQTRSSVAPYLNNRAPLRPNPYIELPLGAIKPQGWLNEMLVRQKTGMTGQLDKLYPLVMNQRNGWLGGDGDQWERGPYWIDGLVPLAYILNDSTLIARAKPWIEWTLNSQQPDGYFGPKTDYPHERGIQRNNSRDWWPKMVMLKVLKQYYSATSDKRVIRLMTNYFRYQLKELPTKPLDHWTFWARYRGGDNLQVVYWLYTITGDKFLLDLADLIHKQTFDYTGAFLAGDLLTTPGSIHCVNLAQGFKEPLVYYQHRPDARYLNASKKGLADLRRFNGMAHGLYGGDEALHGNNPTQGSELCSAVEMMFSLESMLTITGDVTYADQLEKIAFNALPTQATDDYMGRQYFQQANQVMLTRHVRNFDVNHGGTDLCMGLLTGYPCCTSNMHQGWPKFVQNLWYATPDRGLAALVYSPSTVTATVGNGTRVMVDEQTNYPFGESIRFALTLNGGSKTVSFPFHLRIPAWCRKATVLVNGQVVKESAGNQIAVVKRVWQSGDVVELRLPMHIFKNQWHENSVSVERGPLAYALKMGEETQIVRNDKDPIEFGAEYIEVRPTTPWNYGLIETDKQPVEQNARFSSRETTSDYPWNVANAPSEIRLKARRIPSWKLYNEMAGPIPFSVIDYMEVAKEEEEITLIPYGCTTLRISQFPVVR
>NZ_CP014263.1|WP_077130857.1|2044328_2046020_-|sodium:solute-symporter
MSILDWGVLVITLFGIIAYGMIRSRRSRSMDDYLLAGQSLPWYHVGLSVMATQASAITFLSAPGQGFVDGMRFVQFYFGLPLAMVVLSITFVPIFHKLKIFTAYEFLETRFDVRVRTLTAGLFLLQRGLSTGLSIYAPAIILSTILGWNIYWTNLLMGGIVLIYTVTGGTKAISHTHLQQMLVVTLAMVVAGFLTVRLLPESVGFVDALQVAGKAGRMNLIDLKFDPDNRYNLWSGLIGGFFLQLSYFGTDQSQVGRYLTGQSIGQSRLGLLMNGLLKVPMQFLILLVGVLVFVFYQFNPAPAFFNKQETDRLRTSPYAREYQLTEIRHQNLAAQRQRAVLDMQVALKTNDEAGQQAANAMLQETDVALKTVKADVVKLIDKNNPAADTNDANYVFLRFVLDHLPHGLIGLLIAVIFSASMGSIASAYSSLASTTVVDVYKRLVSTNGSDADYLRASRWATVGWGVFCIVVAQFANRMGSMIEAVNILGSLFYGVILGVFVVAFYMKQIGGRATFWAALIGQVFVVLSWYFDLTAFLWLNAIGCVLVMGFAWLLQRVLGADRS
>NZ_CP014263.1|WP_077130858.1|2046199_2047420_-|hypothetical-protein
MKTVLLGLFAFLPSLLFAQTYKVTPDDLARRQSYLLMRDGSTVRGQILRQDSILISVRKRNGNMSFVEADQVIRVVGDAAAVPKPAFGSENTILPYQVFVMRDGARVEGTFVRRDSTMITVRKRNGQLTYFEPELLLRTDTLSMETVGELTGMSPNRFAPWLLTGNTAHNAEKGRFYYRNTWLSRHELQYGITRFWSVGATFITPIPYLATAENYYGSGLYSWNMPRLYTQLSAGVGPLFRAGVNASFTANQLIGSSKTGGQFTLQGLLSFGSSQNNVTLGYSIAVPKFKYVLYPAWPSFSSSMPPQPVSVSVANQQLLSFGVIKKVSPKLTVVSDNSVSLGKQYRYYSYADGRARVSLALRFDRKRHAFDAGAYMLIYEKPFLWEGDKKARLFPYIGYNLIIGKD
>NZ_CP014263.1|WP_077130859.1|2047461_2048739_+|aspartate-aminotransferase-family-protein
MQTVTHRQLFFQHIAQTSDFPLALEIDRAEGIFIYGPTLGGSAEGAAQQPKRYIDLISGIGVSNVGHRHPHVLQAIQTQLDKYLHLMVYGEYVQSSQTQLAHALAQTLASHTGPVGVLDNVYFTNSGTEAVEGAMKLAKRYTGRTEIISCLNAYHGATQGALSLSGDENFKRNYRPLLPGVRHINYNNWADIEKISCRTAAVVMEVVGAESGVRVPDAGYLQAVRQRCTDMGALVIFDEIQTGFGRTGTFWAFEGAGENGTAVVPDVLLCAKGMGGGMPIGAFISSAAVMSVFKNNPVLGHITTFGGHPVSCAASLATLQVIRDEKLYADAEAKGQLFRQLLVHPAIREIRGKGLMLAVEFESFDVLKPIIDRAIQPGESTPGESTPGVITDWFLFCDNSMRIAPPLIITEEQIREACAVILGAI
>NZ_CP014263.1|WP_157579179.1|2048808_2049642_-|hypothetical-protein
MFYTLGSSTLAQQPPKIQIMLLGSNHFGQAGFYKDAPLADLFIERRQQELQQLRDQLARFKPDLILIEREPTAQSTTDSLYRLYTAGKLALTDLDYGRAETYQIAYALGKTLRHDRIYGVDYYGGTSNRILNQGQGIEYYLDELKTFNVLGSQINEPFRQGKTTVSGYLRQLNAPEVLQKTYHLMFVTPAKVRRGLLNTTDRTLDSSRVSYDYVGADFISHFYNRELRIYANIVATQLAQKKQRILVVMGQRHAAVLTKIFENDPDYTLVPVGDYLK
>NZ_CP014263.1|WP_077130861.1|2049989_2051564_-|acyl-CoA-carboxylase-subunit-beta
MQTETQPALNARLSNVDILAQKNAEAELGGGQKRIDAQHKKGKLTARERIALLVDENSFEEIGKFVMHRTRDFGLDKEHYLGDGVVTGYGTIDGRLVYVFAQDFTVFGGALSETHAEKICKIMDLALQNGAPVIGLNDSGGARIQEGVLSLAGYADIFYRNTRASGVIPQLSAIMGPCAGGAVYSPAITDFIFMVEQTSYMFVTGPNVVKTVTHEEVTAEELGGASTHSTKSGVTHFACANELACIQHIKQLLSYIPQNCEDDAPRLPYEPGDESRPALNSLIPDNPNQPYDMREVIDELVDGGSFLEVHKNFAENIVVGFARIGGRSIGIVGNQPAVLAGVLDIQASAKAARFVRFCDCFNVPLLVLEDVPGFLPGTDQEWNGIITNGAKLLYAFCEATVPRITVITRKAYGGAYDVMNSKHIGADMNYAWPSAEIAVMGASGAAEIIFKREIAEADDPQAKLHEKVQEYTEKFANPYRAAHRGYIDEVIMPDQTRQKLLRAFGMLENKVATLPKKKHGNIPL

Crispr_ID: NZ_CP014263_3

• CRISPR_ID: NZ_CP014263_3
• CRISPR_location: 2174159-2174280
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 2 spacers

Consensus repeat of NZ_CP014263_3

Consensus_repeat	Method
CGCAACCCTTTGCGTCTCCACGT	CRISPRCasFinder

spacers of NZ_CP014263_3

>3.1|2174182|20|NZ_CP014263|CRISPRCasFinder
CGGATGGTCAATTGTAGAGA
>3.2|2174225|33|NZ_CP014263|CRISPRCasFinder
GCGTCAGCAACCCTTTGCGTCTCCACCTGCGTC

CRISPR arrays and Neighbor proteins around NZ_CP014263_3

CRISPR arrays

The CRISPR arrays of NZ_CP014263_3

>merge|NZ_CP014263|3|2174159-2174280|CRISPRCasFinder
CGCAAAGGGTTGCGTCTCTACGCCGGATGGTCAATTGTAGAGACGCAACCCTTTGCGTCTCCACGTGCGTCAGCAACCCTTTGCGTCTCCACCTGCGTCAGCAACCCTTTGCGTCTCCACGT

>NZ_CP014263|3|3|2174159-2174280|CRISPRCasFinder
CGCAAAGGGTTGCGTCTCTACGC	CGGATGGTCAATTGTAGAGA
CGCAACCCTTTGCGTCTCCACGT	GCGTCAGCAACCCTTTGCGTCTCCACCTGCGTC
AGCAACCCTTTGCGTCTCCACGT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014263.1|WP_077130958.1|2186534_2187131_-|tRNA-(ms[2]io[6]A)-hydroxylase	unknown	unknown	gnl|CDD|153119
NZ_CP014263.1|WP_077130959.1|2187232_2187886_+|peptide-methionine-(S)-S-oxide-reductase-MsrA	unknown	unknown	gnl|CDD|376578
NZ_CP014263.1|WP_077130962.1|2190057_2191128_+|hypothetical-protein	unknown	unknown	gnl|CDD|367122
NZ_CP014263.1|WP_083732805.1|2172917_2174072_-|DUF4249-domain-containing-protein	unknown	unknown	gnl|CDD|379442
NZ_CP014263.1|WP_077130960.1|2188067_2188775_+|hypothetical-protein	unknown	unknown	gnl|CDD|237000
NZ_CP014263.1|WP_157579183.1|2170124_2171423_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130948.1|2167641_2168892_-|hypothetical-protein	unknown	unknown	gnl|CDD|237617
NZ_CP014263.1|WP_157579318.1|2176788_2178036_+|DUF4249-family-protein	unknown	unknown	gnl|CDD|379442
NZ_CP014263.1|WP_077130946.1|2164165_2166532_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP014263.1|WP_077130945.1|2162767_2163652_+|Rpn-family-recombination-promoting-nuclease/putative-transposase	unknown	unknown	gnl|CDD|372314
NZ_CP014263.1|WP_077130957.1|2185507_2186524_+|alkaline-phosphatase-family-protein	unknown	unknown	gnl|CDD|277335
NZ_CP014263.1|WP_077130955.1|2178330_2181294_-|PD-(D/E)XK-nuclease-family-protein	unknown	unknown	gnl|CDD|378929
NZ_CP014263.1|WP_077130947.1|2166575_2167613_-|DUF4249-domain-containing-protein	unknown	unknown	gnl|CDD|379442
NZ_CP014263.1|WP_077130943.1|2160835_2161693_+|sterol-desaturase-family-protein	unknown	unknown	gnl|CDD|225546
NZ_CP014263.1|WP_077130961.1|2188891_2189920_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130953.1|2174300_2176712_-|TonB-dependent-receptor	unknown	unknown	gnl|CDD|238657
NZ_CP014263.1|WP_077130944.1|2162142_2162562_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077130951.1|2171532_2172732_-|DUF4249-domain-containing-protein	unknown	unknown	gnl|CDD|379442
NZ_CP014263.1|WP_077130956.1|2184823_2185402_-|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl|CDD|223736
NZ_CP014263.1|WP_083732804.1|2168947_2170096_-|DUF4249-domain-containing-protein	unknown	unknown	gnl|CDD|379442

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP014263.1|WP_077130958.1|2186534_2187131_-|tRNA-(ms[2]io[6]A)-hydroxylase	gnl|CDD|153119	cd07910, MiaE, MiaE tRNA-modifying nonheme diiron monooxygenase, ferritin-like diiron-binding domain. MiaE is a nonheme diiron monooxygenase that catalyzes the posttranscriptional allylic hydroxylation of a modified nucleoside in tRNA called 2-methylthio-N-6-isopentenyl adenosine (ms2i6A). ms2i6A is found at position 37, next to the anticodon at the 3' position in almost all eukaryotic and bacterial tRNA's that read codons beginning with uridine. The miaE gene is absent in Escherichia coli, a finding consistent with the absence of the hydroxylated derivative of ms2i6A in this species.	3.75776e-87
NZ_CP014263.1|WP_077130959.1|2187232_2187886_+|peptide-methionine-(S)-S-oxide-reductase-MsrA	gnl|CDD|376578	pfam01625, PMSR, Peptide methionine sulfoxide reductase. This enzyme repairs damaged proteins. Methionine sulfoxide in proteins is reduced to methionine.	1.93312e-83
NZ_CP014263.1|WP_077130962.1|2190057_2191128_+|hypothetical-protein	gnl|CDD|367122	pfam02541, Ppx-GppA, Ppx/GppA phosphatase family. This family consists of the N-terminal region of exopolyphosphatase (Ppx) EC:3.6.1.11 and guanosine pentaphosphate phospho-hydrolase (GppA) EC:3.6.1.40.	0.000145913
NZ_CP014263.1|WP_083732805.1|2172917_2174072_-|DUF4249-domain-containing-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.	3.94806e-30
NZ_CP014263.1|WP_077130960.1|2188067_2188775_+|hypothetical-protein	gnl|CDD|237000	PRK11855, PRK11855, dihydrolipoamide acetyltransferase; Reviewed.	0.00627745
NZ_CP014263.1|WP_077130948.1|2167641_2168892_-|hypothetical-protein	gnl|CDD|237617	PRK14131, PRK14131, N-acetylneuraminate epimerase.	1.32456e-06
NZ_CP014263.1|WP_157579318.1|2176788_2178036_+|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.	3.99927e-37
NZ_CP014263.1|WP_077130946.1|2164165_2166532_-|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.	3.29071e-18
NZ_CP014263.1|WP_077130945.1|2162767_2163652_+|Rpn-family-recombination-promoting-nuclease/putative-transposase	gnl|CDD|372314	pfam12784, PDDEXK_2, PD-(D/E)XK nuclease family transposase. Members of this family belong to the PD-(D/E)XK nuclease superfamily. These proteins are transposase proteins.	4.9615e-29
NZ_CP014263.1|WP_077130957.1|2185507_2186524_+|alkaline-phosphatase-family-protein	gnl|CDD|277335	cd07389, MPP_PhoD, Bacillus subtilis PhoD and related proteins, metallophosphatase domain. PhoD (also known as alkaline phosphatase D/APaseD in Bacillus subtilis) is a secreted phosphodiesterase encoded by phoD of the Pho regulon in Bacillus subtilis. PhoD homologs are found in prokaryotes, eukaryotes, and archaea. PhoD contains a twin arginine (RR) motif and is transported by the Tat (Twin-arginine translocation) translocation pathway machinery (TatAyCy). This family also includes the Fusarium oxysporum Fso1 protein. PhoD belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	4.83707e-60
NZ_CP014263.1|WP_077130955.1|2178330_2181294_-|PD-(D/E)XK-nuclease-family-protein	gnl|CDD|378929	pfam12705, PDDEXK_1, PD-(D/E)XK nuclease superfamily. Members of this family belong to the PD-(D/E)XK nuclease superfamily.	6.78973e-22
NZ_CP014263.1|WP_077130947.1|2166575_2167613_-|DUF4249-domain-containing-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.	2.38103e-37
NZ_CP014263.1|WP_077130943.1|2160835_2161693_+|sterol-desaturase-family-protein	gnl|CDD|225546	COG3000, ERG3, Sterol desaturase [Lipid metabolism].	1.05414e-42
NZ_CP014263.1|WP_077130953.1|2174300_2176712_-|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.	7.97243e-18
NZ_CP014263.1|WP_077130951.1|2171532_2172732_-|DUF4249-domain-containing-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.	2.4967e-34
NZ_CP014263.1|WP_077130956.1|2184823_2185402_-|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].	2.724e-24
NZ_CP014263.1|WP_083732804.1|2168947_2170096_-|DUF4249-domain-containing-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.	2.10556e-40

Protein sequences

>NZ_CP014263.1|WP_083732805.1|2172917_2174072_-|DUF4249-domain-containing-protein
MTLMTKLIRLVLWLLVIAVSLAACIDPYEPDANYNLDVLVIDGFLTDLDEPQIVTLNRSRTEKLTGRFGVLPVSRAALTLLIDGQQTVAFSETAPGTYQLPTGIRGQAGRRYQLQLLLSDGTRYVSTEEVMPTAPAISRVYQRFNSASIVATNPARLLPANDFFIDTNDPAKQPNFYRWDWKAWEKQPWCRSCYQGRYQIFDDQQRLVEGCVTNFTIQGYLDYSCRTPCWEILQSTQLNLLADIYTDGRTIGGRLVGQIPYLHAGPCLVEIRQVALTKEAFMYFRQLEVQTQNAGGLADVPPNAPIGNVRNLANEREAVVGYFGATSVARVRYWLNRSANTGPPIANTLFEAQTGRIPQEDGRVAALCVPGPTRTPIKPEGWQE
>NZ_CP014263.1|WP_077130951.1|2171532_2172732_-|DUF4249-domain-containing-protein
MKPIARYAVIAFLSMLIGCIDPIAPRFNLTADVLVVDGTITDRAEPQRIRLNRSAADRFTGRFGDTPLTGARVTVRVNDDETITAREVSPGTYQLPDGFRGRVGNRYQLQLELADGMRYASSTETMPAVSPILTTTDVYNPRSLTGQLSPLTAANDLFIDTQDPAGTPNYYRWDWVLWEKQDFCQTCGNDQVYYERDDAGNLVEKCMPNRIVPLPFPRPQNIDYECRTQCWEILYSSQLSLFSDALSDGKRITNRRVAQIPFYQYYPALVEIRQSALTAEAYRYFRRLDEQSQQTGGLTDTPPAAPVGNIRNLSNDREEVVGYFTASGVSAVRYWLTRRNVTNELPASPADPDRPKLFTYLNGRTPYKEPVSGIRGRPPLALCVPGPTRTPIKPEGWQE
>NZ_CP014263.1|WP_157579183.1|2170124_2171423_-|hypothetical-protein
MLILFAGCRTTEPVPVVVQPDPVTASQASLVSVQATGASSAEVIVKSIRMEPSGWRLTAQTGQGGVVPFTVGETQTLRDFMLTSLRLSGLTVGQTYQLRLAFRFADRDSITALRTYTHRLNNSPTGGPRWTRLAHASFSGGDYTTCPVAVDGICGSNPMNGCGNPTIGAYVGNQVQVVRYAGPTQPFMDVKIYNRQADEWQLLSADRRTPRHGFVQYNVFFQGVDRHQFSGLGYIIEERSASKYFFFRGMGAIFPVGGSPVNPSYGGEDGELVFFTTTDEAYFLTQNGSPAMRSIDAVFTQTVRAPLPEPPGLMATFSIRNIGYVVNQRPGQPTRLWAYNPATDSWTKRADFPGDARQRGVGFAMARQGYFGLGVTAEGRGCATSGSMTLWPTAGSTSRTIRVRAISLWPSSVHPTGPGLSGLMWAGATKRS
>NZ_CP014263.1|WP_083732804.1|2168947_2170096_-|DUF4249-domain-containing-protein
MHRLVGTNAMNFLGHRYTQRQYRYAGAGDAQRKKSFVYLCVTTFFCLTTLSCINEVQLPIRQMERRLVVDGLITDEPPPYPIKLTYSGNLSRSLLIPDELAINGAVVFVDDNLGNRTQLLQDPLNPAFYWLRDARLRGVPGRSYTLRVTLPDGTRYQSRPERMAPVPELERVYGEYRESDRNTSQLNTFLVRIDTQDPPTPGNYYRWQAMCYMPVWSGSDPLRGRGAISYAPFYGLLTNVLSDQLINGNRVAGRLVLTPPLVGLGAQYVEVRQYSLSREAYQYWTRYEQQLARSGTLFDAQPASIEGNVYAAGDSTRLALGYFGVSAVSRRRIVMETDTLDYNDFVARFGPVLFSNTPPSVPGLAREQTQAAPPPNWLTYGR
>NZ_CP014263.1|WP_077130948.1|2167641_2168892_-|hypothetical-protein
MKKLCIWMLLLLAVSCGPTEPVPLAEVLPNILSPTLVSVNTTSSEQAEVVLKTGSEFGATDWHLTMTDASDRPVALSINPVLRLGLFNIVPCRVTGLRPEQTYRLRMRTRNAGGDSVRIERTYTHRTSGPRWLRLAHAPIDQGDFAGTAMSTDNITESEETKLLSVSQNGFYAKRLDYLVPNNEWVVRSSTTGGRSHRTVRYRLQAEAGLVYDFAGLGFLSDELRPGQRQYLKSMVSSGLVVPFYAGPDGELRWFATRDRAYQLTDGSQELWVRQGNWAQYRTADLPEPTGTLATFRIGSTGYAVNQRSGQPAHLWAFDTKTEQWSRRADFPGPARSLGVGFTVAGNAYFGLGINPNEETLRDIWQYDPLGDRWQYVTDYPGQGSTYVVVAQMQRGRTFLGWGYEQQPTGVGAFGW
>NZ_CP014263.1|WP_077130947.1|2166575_2167613_-|DUF4249-domain-containing-protein
MNKLLIACLCVLLMTCVQEVQLPIRQVDRRLVVEGLLTNEPFPWVRLTYSGRYNSNNPSPPQLVVNDALVVLQDDLDRSVRLLPDPFALSYYTPRDSTFRGEVGRTYTLYITLPDGTRYESRPERLNPVPVLEPLRATLRQGVPETGQPDFYDIRIDTQDSPTPGNYYRWSALGWVRRWVQSDPKNPRIPCNTCSCWIPDYGPPGDVLSDALINGNRITQRLVYSLPVLAIAPQYVQVEQFSITQAAYQYWTLFEQQRTRTGSLFDAQPASIEGNVRAVNDTTIRALGFWGASAVSRRRITIAGDTINYDRFLVRYGKLFILPTGDCFSNFSNPILVPPRGWPAR
>NZ_CP014263.1|WP_077130946.1|2164165_2166532_-|TonB-dependent-receptor
MKKLYALIGLLTLLLFGGLTAHAQKRFVISGEVIDGTTRQPLPNVSVVDAKQGAGTRTDSAGQFSLRVLPGPYNLTFSAVGYYARSRFIDMSRGDAYLDITLNPDIRELAQVEVKGRAPDANVTAAEMSVVRLDMKNLKNIPVVFGEVDVLKALLLQPGVTSVGEGAAGFNVRGGAADQNLVLLDGAPIFNTSHLLGLLSNLNADAIQDVTLYKGGIPAQYGGRLSSLLLLNTKPGNDERLSITGGIGLITSRLLANGPLTKNKKLTFVAGGRVAYPNLMLGLFPDPTRRNRASFYDLNGRLTYRLAEGSQLTATAYHAYDSFKFPQDTVFGWQSTLATLRWSQRLTPRLSLNAGASHSDYRFFLDGLTSRNTYRYQSEIRQQDARLDWLFTPNRHRLEWGGSLTSYRIRPGSIQPTGTDTNINPQTLPTEQAVESAAYVSDEWTPVRWLSVQAGVRYVQFTNRGPGVVYQYAEGLPRSRETITDTLQIGAGQTIAQYGGWEPRLTVRATVAANTSLKLSYNRTRQYLHLISNTTSISPVDFWKLSDALVPPQLADQWAVGLFRNFRENMYEASVEVYQKQLTDLVEYRNGATLLLNPALDADLLRAQGRAYGAEMSVQKTRGLLTGLLAYTYARTFARVNSPYAVDQINAGNWYPATFDRPHNLTVSTQWKWKRGWTFGTNFVYTSGRPTTYPDGTYRLNGVVVLDYSQRNADRIPDYHRLDVSFSKDGRRTPGQRRYSNWSVSLYNVYARRNAYSIYFQRVNTTTRSYQLSVFGTVIPSVSWNLTW
>NZ_CP014263.1|WP_077130945.1|2162767_2163652_+|Rpn-family-recombination-promoting-nuclease/putative-transposase
MDLYNDNERFISILSDYGFKVTFGNESDTRFLRRALQALIQSPATITQVEFIESEIPGLTRDSRSGVYDLACVDERGNQFIVEMQLSKYPDFIQRMKFYSFYRLNTLVRKGKYKFEGLPRIYCIGILAFDIFPHVGDYHNVAMLRNEKGELIDDQTTFITVELAKFKKRLANVQTDLDKLIYTMKATHKATKPKQFPQFWNEEWLEAAIKELDTRQMTPEKRMAYEMTLSANALAVENENRKIEEAEERREKLVKTETVTKALKRGKLTIEEIAEDSGVSVDFVLEIQRGLIKN
>NZ_CP014263.1|WP_077130944.1|2162142_2162562_+|hypothetical-protein
MSFQNLLATLTALGLGAILTKFFEYASDRQKTKEQTKHDFKQTRYKAIILLMYSLLDFEKQNKMLQQNNRHFTDKTELWEELKAEWTNMTLYASDNVVRAMKQFLREPTLDSYNVTTLAMRKDLYNIKTKLTLEDLRLD
>NZ_CP014263.1|WP_077130943.1|2160835_2161693_+|sterol-desaturase-family-protein
MRDLIQYAIPGFVVLLVAEVLVTAHQQKDYYDAKDTASSLAMGIGNVIVGLVGKVIVFGAYSFVYQFRLFTIDMSQWWAWVMLFFADDFSYYWFHRISHSSRYFWASHVVHHSSQKYNLGTALRQTWTGALTGAWVFWLWMPLLGFSPVAVMTMQAISLLYQFWIHTELIDKLPAPIEFVFNTPSHHRVHHGSDLDYLDKNHAGILIIWDRLFGTFAPEKQRPTYGLTKNIDSYNPVRIAFHEWTDILRDLRRAGSFRNALGYLFGPPGWSHDGSRKTTKQLRGE
>NZ_CP014263.1|WP_077130953.1|2174300_2176712_-|TonB-dependent-receptor
MSRRLLFLILLMNLTGLAQAQILYTLSGTVRDSATGQPLVRAAIVLNYEKASSGTYTDDEGRFSIKVAAGRHVVVARHVGYVPFRQSLRIRGNTMLDVRLPSVASQLEEVVVTSKGFDRTVRQPLLGVSQISLKTIQKLPTALGEVDILRSLQLLPGVTSVGEAANGVNIRGGTTDQNLILLDDTPIFNPTHMFGMFSVFPADAVSGLDLYKGNVPARYGGRAASVLDVTLRNPDLNQFRLTGGVSLVSNRLTAEVPIIRQKMAVMVSGRGAVNDFLLPLVLPRFDQIRARFGDLVGKVFWRMNDRHTLTATGYVNRDIFQTDLLGSIANINATATQYDNQTANGMVRWFWAITPRLNLQTSAIVARYTPRILSIEPPTDPAVAANKVVLEQSIWQRQAKTNLGYQTDNHKLEVGLSATHYRLNPGELLPGSSTSVNRQATPLENGLELAVHAEDEWSITPQLAVSAGLRYSYFLNVGPSLVRQYRPGTLPDETTVTDSVRYGAGQVAQTYGGLEPRLGLRYAVGANASVKVGYNLMRQYLQVISNTTTPLPTARWKLADPFIRPQISQLWSAGWFQNLKSNIYELSAEVYWRSTQNVVDYRPGANFLLQPYPETQLLQGRGKAYGVELMLAKKKGELTGWVNYTFARTFNQVAEGASFQERINNGNWYAANFDRPHSLNLSLTINQTKHHSFSFNFVYSTGRPYTAPEGFVRYQGRNYPYYNERNQYRLPDYHRLDFAWNIYNPSLKGRRWQGRWTFTVYNLYGRKNAYSIFFRTEGQATNPYRLAIFAVPIPSLSYNFEFK
>NZ_CP014263.1|WP_157579318.1|2176788_2178036_+|DUF4249-family-protein
MTILLSVILLLFIAVACVDPYQPDFKATVDVVVVDGTINNLPEPQVIQLNRSRADPVTGRFGVLPIRNAKVDIIVNGDQTLSLVETQNGTYQLPSDFKGKVGASYQLRFTLDDGTRYESTPEVMPAVVPISRLSHRFNANSLPAKRPDGQPSRVRDATDIFVDWQDPPSTVNYYRWNWILWERQAWCRSCGNGYYLIWNRNNTNLLYEDCYTLQNTGSVSGPSPPYFINDYRCRTPCWEILYGYDINLFDDAFSNGGQLTGRLVARIPFYQSEGCLVEIRQASLTRQAHRYFQQLQQQTQNSGGLADTPPAAPIGNIRNKTNQAEAVVGYFTAAGISAQRYWLDRLDATGNPPGLFQALNNLEPSPEDILVDPNNDRGKPAPDFVGGTKNQSRPPTAVCEPSDSRTPFMPAGWRE
>NZ_CP014263.1|WP_077130955.1|2178330_2181294_-|PD-(D/E)XK-nuclease-family-protein
MTFLQQTAQRIYEAHGPSMADVWVILPTRRAVSVFLDELAAQSDRPFLAPHAMAVDDFITQAAGVQLIDSVSLLFELYDVFKDIDPQVEFEQFIGWATVLLADFDRIDQYLVDPHELFSYLTAAKALERWQVNVPSSAQPITETLGTTRYFKLFENLHTTYHALRQRLTEQGLAYRGMAYRLLADNVESLIRDNYAYERVYFVGFNALSAAEEHVIRVLVDARKAELFWDADLYYMNDRRQEAGQFLRRYRENGWFFAKQNHADLRDLSNNLLSTEKNIRVVGVPNASMQAKVAGALVQSAGSGKTAIVLADETLLVPVLYALDESVTDLNVTMGLSLRSSLLFTLVDTLFEMQRTVHEFRTKDGRNLRLPKFHHRHVVKVLNHPFVKQYERISGLMGPEEVNEKGEVLPPEPLFQWMAKDIVKQQRVYLTERDLREMGQNDPLVRVLFARWPDDKPDRVIRTFYDLVDLLRDVYRASQDAIEIEYLYLFYTLLRQLETTLERQALTPEGRTPVTVKSFRQFLYELIRQTTIPFTSEGNSQLQVMGMLETRALDFDRVIILSVNEGVLPQSRRLNSLIPFDIAHELKLPTYREQEAVMAYHFYRLLQRASDIVLIHTTSTDAYGNSKGEPSRFIRQIEHELVPLSGGRIRLSRPTVRFGQMNAAKVADVSELEVPKTESIRDEIQKLLTTKGLYPSYLNQFLRCSMSFYFSRVVNISEEEDIEEKMGAVDFGNWMHKVLERLDIEYRLKELPVEEPLVIRLLEEEFSNTMKGRVIESGMNLLLYDLAKKLMLDFQKQQGNLPGLTVIGTEQTLETYLDVPMNGHEPLHIRIAGKIDRIERFGDQIRIVDYKTGNVKLSDKTPANLREKLLDDGKEDKMRQLWLYRYLAIKNIRDHGGLPRDKAKRDIFPAAGMPVEAGFYSFRDVQGGFKTNPVRFTATDDPDQYIADSEDLLRQLIHRMLDMNEPFRKTDQLDRCEYCNFKGICGR
>NZ_CP014263.1|WP_077130956.1|2184823_2185402_-|Crp/Fnr-family-transcriptional-regulator
MTTDILTDYLITQSPKACLRKRLERGDYIYKPGDDAPYVYLLEKGVVKIGSLGPLGERVVYDVLRPGEVFGDLDYLDEVEFFEFAQAATSLSIVVVQLSFFRHIIIHDPVVAEWFNETIVRRWYKAEMRLLHRAHETVENRLYRLKEQHIQVVKDADGLAHQVLQLLSHQEIADLVGATRQTVSKKLRRMPV
>NZ_CP014263.1|WP_077130957.1|2185507_2186524_+|alkaline-phosphatase-family-protein
MKNLILLSLCASFLFSGCRTSQSNSAAPPKRASVIAFGSCSDQKRPQPLWDDIVAQKPDVWIWLGDNIYGDSENMDTLTAKYARQKANPVYGQLRQSASVIGIWDDHDYGVNDGGKEYPRRRESQQLMLDFLDEPANSPLRSQEGAYSSHVYGPVGQRVKVILLDGRYFRDPLKKEGKVNVPDPSGDILGEAQWQWLEQQLTNSDADVHIIGCGIQFIPEEHPYEKWANFPTARQRLMNLLGKTKPKGAILISGDRHIAEISRESVPGLGYDLFDITSSGLTHVSKPHDEPNRHRVGNMITKLNYGLITINWQQKPLTATVRINGDEQATYLTQEIRF
>NZ_CP014263.1|WP_077130958.1|2186534_2187131_-|tRNA-(ms[2]io[6]A)-hydroxylase
MSLTTLGLELPTDPRWVNIAEMNIGDILIDHAYCEQKAASSCISLIVSYSDKEELVETLTPVVAEEWGHFQRVLKELRKRNIPLGRQRKDEYVNQLRSRLRRSTGDQNEQLMDNLLINALIEARSCERFKLLSEHIADEGLQKFYRELMISEAGHYRNFIELAETYLPAERVRQRWKEFLAVEADIIASLDLRGDRMH
>NZ_CP014263.1|WP_077130959.1|2187232_2187886_+|peptide-methionine-(S)-S-oxide-reductase-MsrA
MKALTSLLLVFVLVAGCRQQTSQATTEKDTRPAKLPALQPGEAVATFAAGCFWCIEEEFELLRGVREVVSGYSGGDLENPTYEQVGTDQTGHAEAVQIYYDPKIIPFDTLLTAFFAGHDATSLNRQGPDIGTQYRSIAFYRTPAEKEAINAAIKRETASGRHQRPIVTEVVPFKAFYPAEVYHQGYYRLHPNELYVQTVSKPKVEHFKERMSAWLKE
>NZ_CP014263.1|WP_077130960.1|2188067_2188775_+|hypothetical-protein
MPEPEPSLGRKILSFFIKSEETADKPATGTAPASVPASPRPAAVPAPAATTGPAPTPSTQPGSIDTKFAEHFADVLAQNNPPGPDYFEFRETLRSLSNLGLTEEKQYQAAWASFKALAGTADINLLTNTAKQYLTALNKDRDGFGKSVEAAISERVGGLQNEQKRLQTENESLAKQLLAIQQQIDANNNRLGAIGGDIAEQSAKINQNRENYDATFAHFTNQINADINKMTQYLK
>NZ_CP014263.1|WP_077130961.1|2188891_2189920_+|hypothetical-protein
MATPDFSQLGGNTEPEKKSFWSRPEGILGMIALAGLAGFALVNVNQILEFLIRATSNVLELALLLGVLGVVIFLITSRDVRTAVFFLFKSLMRTLTGTVIQLNPIAIMKIYIDDLKKKRREMQGQIDTLAGQLVKLNKRINDNNESIKQKFAEANKANNMADRPGMREQAQLATIEGAGLQEMNEKLLPLQRNIQMVLAFMEKVNQSADYIIKETEIKVRLKETEYQIVKESSNALKTAVSIFKGDPDKKFYFDESMEYIQDDMSRKLGEMKRAMDLSMDFINGVDIQNGILSDKGQALLEAYNKGEFKMVQLDAPKANPITAPQPGQLNPPKDAGYRNLLD
>NZ_CP014263.1|WP_077130962.1|2190057_2191128_+|hypothetical-protein
MQRLTVAGRLLITALILAAIFFGFRYFGGSEALRKLAPGVDSPKQESESATMPRAEDQTSSTSADESTASDNGSSAGSSDESSASSGARRTFTYTPPAPQNGKLKGVVELGASGFNSFIVRVDADKNWKLEKAEFGNSLVMENMATDDDIRAGLKSYIGKMLDFGVGGRDIQFVVSSGAVKAEGTQKIIKALKSLNYVVNTVTPEQEGSLGLRAVLPADYADNSFVVDIGSGNTKISWKENGQTKAVETHGSKYFQNGMSDETVASEVGAKAKQVPTSHRKTCFIIGGVPFELAKAVRNGKERYTVLDAPSAYKLENAKSKAGLNIYKAIADATGCDQFVFDWDANFTIGYLLTLK

Crispr_ID: NZ_CP014263_4

• CRISPR_ID: NZ_CP014263_4
• CRISPR_location: 3424944-3429101
• CRISPR_type: Unclear
• Repeat_type: NA
• Spacer_info: 56 spacers
• Cas_protein_info: cas4,cas2,cas1,cas6,cas3,cas5,cas7,cas8b8

Consensus repeat of NZ_CP014263_4

Consensus_repeat	Method
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CRISPRCasFinder
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CRT
GTTTCAATCCTGCTTATCAATGGATTAGCTCTCGAAT	PILER-CR
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	PILER-CR
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CRISPRCasFinder

spacers of NZ_CP014263_4

>4.1|3424981|35|NZ_CP014263|CRISPRCasFinder,CRT
GCGATGTCGAAGCTACCCGCCGTGCTTGAAGCGGG
>4.2|3425053|42|NZ_CP014263|CRISPRCasFinder,CRT
TTTCGGCGGCTTTGCGTTCGATGATACCCACGAAGAGCGTAG
>4.3|3425132|37|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
ATGTCCTCGGCGCACATTATTACCTCGGCGCGGCAGT
>4.4|3425206|38|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
GCGCATGTCGGCCTCCGGGTTTGCCAGCAACTGGTACA
>4.5|3425281|36|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
CGTCAGCAGCCCCGGCATTCGGGCCATTTCCATTCT
>4.6|3425354|37|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
ATATGCTTATTGACTATATCCGAAATCCCGATTTAGC
>4.7|3425428|37|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
CCTGCTGGCAGTGGTGGCCGGTGGCTTAATCCTTTAC
>4.8|3425502|36|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
CTGGAGCAATACCGAGAGTTTACCATCGGGCTATAT
>4.9|3425575|38|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
CCGGGTAGTTCCGTAATGCACACAAGCCGACAGAAAAT
>4.10|3425650|36|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
CAAAACCAAAGCCGGGGCCAGCATCGACGTAGACGA
>4.11|3425723|38|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR
CCGGCCACGTGGTTGCGCGGCAAGTACGATAACGATTA
>4.12|3425798|37|NZ_CP014263|CRT
AACCGACCGCCGAGGGCCGGGCCTACGAGGAAAAAAT
>4.13|3425872|26|NZ_CP014263|CRT
GTCATGGACAAACTCGCTCAGTACAC
>4.14|3425935|39|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CGTCTTTGCCCGAAAAAAACACGTACAGAATACTTTCGG
>4.15|3426011|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CTCGATTGAGCCGCTGGTTAAGTTTGTGGAAGAGTA
>4.16|3426084|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
GGCCTACGCCAAGAGTGCACGCAGTTCGGGCATCGA
>4.17|3426157|38|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CTGATTCGGGATACCAACGAAAGCCACGGCGGTACGGG
>4.18|3426232|35|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
AACCGGAACAGCTTCGTGCAGGTTGAAGCCCATGA
>4.19|3426304|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
ATATACATTTGTGTCAACAAGCCGGGAAACATTCGAG
>4.20|3426378|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
AAGTCCAGCAGGGCCAACAGATCCACGCGCTGCTCAT
>4.21|3426452|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CTTCCAGATCGTGGGGAGCCTCTTTGGTGTCTACTT
>4.22|3426525|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CGTGTTTGCCGGTTCTTTGTACGTAGGGGCTTCACCG
>4.23|3426599|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TGGCGGCATCACCAATTGGCGCAGCGGGTAACAGGG
>4.24|3426672|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TTGTTCCGTCACCCTTCGCGCCCCACAACTGTACGC
>4.25|3426745|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TTTTTTTCAGGAAAGCATGTCGTCTTCCTGTTGCAC
>4.26|3426818|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CGCGCAGGCGGCAATGGAGCGGGCCACCGCTCCGGT
>4.27|3426891|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CTACACCGAACGCTTCGTAATAGTCGCATACTCGAAA
>4.28|3426965|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TACCTGCGCTATGTGGTGGCCGGTGATCTGGGTAAAG
>4.29|3427039|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
GGGCAATTACGTTACTACCTTCATCGAAGCCTAACCA
>4.30|3427113|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TGATCGTAGATGTGATTCGGGTTACAGTTGCCATCGA
>4.31|3427187|38|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CAGGTGGTCAAACCCTCAATTTTTTCTTGGAGTTCTGA
>4.32|3427262|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TAAACTCCCGAAATTCTTCGCTCATTTGGCGCAAGAT
>4.33|3427336|38|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CCGGCGTATTGCGCTGAATCCTATCAGCCAAAACCTGT
>4.34|3427411|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
AGGTGAAAAAAGGTACATTACAGGGTACGAGTGGGG
>4.35|3427484|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CAAATAGTGTTGGCAGATGTTGGCAGGCTGCCGAAT
>4.36|3427557|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CTGGTTGAGAGGTGGTTTACCCACAAATCCGCATACG
>4.37|3427631|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
AACAACGACTCAACCATTTGCTTAGACACTTTCATGT
>4.38|3427705|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CTGGCCCCCGTCGTCAGCTTTGAGCCGGGGGGCGAAA
>4.39|3427779|38|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TCCGTTGTGGACGACGCCATGCCGGGACTACTCGGACG
>4.40|3427854|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CGTAGGCCAGATTGTACGCCAGTCCCGTTAACGGTAT
>4.41|3427928|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
AAGATTGGGTTCCGTTCGACATTGTGTCGAACGACG
>4.42|3428001|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TTTCTTCCTTTCGCCATAAGCTAAGTAACTTTTTAA
>4.43|3428074|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
GTTGGAGCGGTTAGTTTACGTATGCGGATTTGTGGG
>4.44|3428147|35|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
ACGCTCAAGACCCGCCCCCTGATGGACGATCAGGG
>4.45|3428219|35|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
AAGCGCGTCGTCTACAGCCGTTAGGCTGACCGTGT
>4.46|3428291|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CGATGGCCGCTATTGGGGTAAGCAGCTACAATACATA
>4.47|3428365|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TTATTGCAGGAATGTGCCTCGTCATTATCTTATTAGA
>4.48|3428439|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
GTCGTTTACCAGGGCAATGTACTCTGTCAGGTACTC
>4.49|3428512|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TTTCTTGTTGTCACCACATATCAGCCCAATGGCGAAA
>4.50|3428586|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CCAACTGAAGCGATACGGCCATGCGTTGATGCCTCG
>4.51|3428659|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CAATCCAGTGGCACAGGTAGCAGGTCGCGCTTTTCGG
>4.52|3428733|38|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
ATGACTCGGTTTTTCAGGTCTCTGATTTGCATGGCTTG
>4.53|3428808|36|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TGGTGATTTAGTAATCTCAATCCCGTAGTGTTCACT
>4.54|3428881|38|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
ACCGTCTGACAGGTTGCCAACGAGCGCGGCTTAGATGG
>4.55|3428956|35|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
CCCAATTCAGGGATACCTGGGTGCAACTCTGCCAA
>4.56|3429028|37|NZ_CP014263|CRT,PILER-CR,CRISPRCasFinder
TCAGAACGTGTAATTTAGCCGTATGTCCAAACGAACA

CRISPR arrays and Neighbor proteins around NZ_CP014263_4

CRISPR arrays

The CRISPR arrays of NZ_CP014263_4

>merge|NZ_CP014263|4|3424944-3429101|CRISPRCasFinder,CRT,PILER-CR,PILER-CR,CRISPRCasFinder
GTTTCAATCCTGCTTATTAGTGGATTAGCTCTCGAATGCGATGTCGAAGCTACCCGCCGTGCTTGAAGCGGGGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATTTTCGGCGGCTTTGCGTTCGATGATACCCACGAAGAGCGTAGGTTTCAATCCTGCTTATCAGTGGGTTAGCTCTCGAATATGTCCTCGGCGCACATTATTACCTCGGCGCGGCAGTGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATGCGCATGTCGGCCTCCGGGTTTGCCAGCAACTGGTACAGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATCGTCAGCAGCCCCGGCATTCGGGCCATTTCCATTCTGTTTCAATCCTGCTTATCAATGGATTAGCTCTCGAATATATGCTTATTGACTATATCCGAAATCCCGATTTAGCGTTTCAATCCTGCTTTTCAGTGGATTAGCTCTCGAATCCTGCTGGCAGTGGTGGCCGGTGGCTTAATCCTTTACGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATCTGGAGCAATACCGAGAGTTTACCATCGGGCTATATGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCCGGGTAGTTCCGTAATGCACACAAGCCGACAGAAAATGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCAAAACCAAAGCCGGGGCCAGCATCGACGTAGACGAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCCGGCCACGTGGTTGCGCGGCAAGTACGATAACGATTAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAACCGACCGCCGAGGGCCGGGCCTACGAGGAAAAAATGTTTCAATCCTGCTTTTGCTCTCGAATGTCGCAGGGCGTCATGGACAAACTCGCTCAGTACACGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATCGTCTTTGCCCGAAAAAAACACGTACAGAATACTTTCGGGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATCTCGATTGAGCCGCTGGTTAAGTTTGTGGAAGAGTAGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATGGCCTACGCCAAGAGTGCACGCAGTTCGGGCATCGAGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATCTGATTCGGGATACCAACGAAAGCCACGGCGGTACGGGGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAATAACCGGAACAGCTTCGTGCAGGTTGAAGCCCATGAGTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAATATATACATTTGTGTCAACAAGCCGGGAAACATTCGAGGTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAATAAGTCCAGCAGGGCCAACAGATCCACGCGCTGCTCATGTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAATCTTCCAGATCGTGGGGAGCCTCTTTGGTGTCTACTTGTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAATCGTGTTTGCCGGTTCTTTGTACGTAGGGGCTTCACCGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTGGCGGCATCACCAATTGGCGCAGCGGGTAACAGGGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTTGTTCCGTCACCCTTCGCGCCCCACAACTGTACGCGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTTTTTTTCAGGAAAGCATGTCGTCTTCCTGTTGCACGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCGCGCAGGCGGCAATGGAGCGGGCCACCGCTCCGGTGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCTACACCGAACGCTTCGTAATAGTCGCATACTCGAAAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTACCTGCGCTATGTGGTGGCCGGTGATCTGGGTAAAGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATGGGCAATTACGTTACTACCTTCATCGAAGCCTAACCAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTGATCGTAGATGTGATTCGGGTTACAGTTGCCATCGAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCAGGTGGTCAAACCCTCAATTTTTTCTTGGAGTTCTGAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTAAACTCCCGAAATTCTTCGCTCATTTGGCGCAAGATGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCCGGCGTATTGCGCTGAATCCTATCAGCCAAAACCTGTGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAGGTGAAAAAAGGTACATTACAGGGTACGAGTGGGGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCAAATAGTGTTGGCAGATGTTGGCAGGCTGCCGAATGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCTGGTTGAGAGGTGGTTTACCCACAAATCCGCATACGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAACAACGACTCAACCATTTGCTTAGACACTTTCATGTGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCTGGCCCCCGTCGTCAGCTTTGAGCCGGGGGGCGAAAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTCCGTTGTGGACGACGCCATGCCGGGACTACTCGGACGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCGTAGGCCAGATTGTACGCCAGTCCCGTTAACGGTATGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAAGATTGGGTTCCGTTCGACATTGTGTCGAACGACGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTTTCTTCCTTTCGCCATAAGCTAAGTAACTTTTTAAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATGTTGGAGCGGTTAGTTTACGTATGCGGATTTGTGGGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATACGCTCAAGACCCGCCCCCTGATGGACGATCAGGGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAAGCGCGTCGTCTACAGCCGTTAGGCTGACCGTGTGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCGATGGCCGCTATTGGGGTAAGCAGCTACAATACATAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTTATTGCAGGAATGTGCCTCGTCATTATCTTATTAGAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATGTCGTTTACCAGGGCAATGTACTCTGTCAGGTACTCGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTTTCTTGTTGTCACCACATATCAGCCCAATGGCGAAAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCCAACTGAAGCGATACGGCCATGCGTTGATGCCTCGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCAATCCAGTGGCACAGGTAGCAGGTCGCGCTTTTCGGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATATGACTCGGTTTTTCAGGTCTCTGATTTGCATGGCTTGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTGGTGATTTAGTAATCTCAATCCCGTAGTGTTCACTGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATACCGTCTGACAGGTTGCCAACGAGCGCGGCTTAGATGGGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATCCCAATTCAGGGATACCTGGGTGCAACTCTGCCAAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATTCAGAACGTGTAATTTAGCCGTATGTCCAAACGAACAGTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT

>NZ_CP014263|4|4|3424944-3425798|CRISPRCasFinder
GTTTCAATCCTGCTTATTAGTGGATTAGCTCTCGAAT	GCGATGTCGAAGCTACCCGCCGTGCTTGAAGCGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	TTTCGGCGGCTTTGCGTTCGATGATACCCACGAAGAGCGTAG
GTTTCAATCCTGCTTATCAGTGGGTTAGCTCTCGAAT	ATGTCCTCGGCGCACATTATTACCTCGGCGCGGCAGT
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GCGCATGTCGGCCTCCGGGTTTGCCAGCAACTGGTACA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCAGCAGCCCCGGCATTCGGGCCATTTCCATTCT
GTTTCAATCCTGCTTATCAATGGATTAGCTCTCGAAT	ATATGCTTATTGACTATATCCGAAATCCCGATTTAGC
GTTTCAATCCTGCTTTTCAGTGGATTAGCTCTCGAAT	CCTGCTGGCAGTGGTGGCCGGTGGCTTAATCCTTTAC
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGGAGCAATACCGAGAGTTTACCATCGGGCTATAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGGTAGTTCCGTAATGCACACAAGCCGACAGAAAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAAACCAAAGCCGGGGCCAGCATCGACGTAGACGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCCACGTGGTTGCGCGGCAAGTACGATAACGATTA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAACCGACCGCCGAGGGCCGGGCCTACGAGGAAAAAATGTTTCAATCCTGCTTTTGCTCTCGAATGTCGCAGGGCGTCATGGACAAACTCGCTCAGTACACGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCTTTGCCCGAAAAAAACACGTACAGAATACTTTCGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTCGATTGAGCCGCTGGTTAAGTTTGTGGAAGAGTA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GGCCTACGCCAAGAGTGCACGCAGTTCGGGCATCGA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGATTCGGGATACCAACGAAAGCCACGGCGGTACGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	AACCGGAACAGCTTCGTGCAGGTTGAAGCCCATGA
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	ATATACATTTGTGTCAACAAGCCGGGAAACATTCGAG
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	AAGTCCAGCAGGGCCAACAGATCCACGCGCTGCTCAT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CTTCCAGATCGTGGGGAGCCTCTTTGGTGTCTACTT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CGTGTTTGCCGGTTCTTTGTACGTAGGGGCTTCACCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGCGGCATCACCAATTGGCGCAGCGGGTAACAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTGTTCCGTCACCCTTCGCGCCCCACAACTGTACGC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTTTTTCAGGAAAGCATGTCGTCTTCCTGTTGCAC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGCGCAGGCGGCAATGGAGCGGGCCACCGCTCCGGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTACACCGAACGCTTCGTAATAGTCGCATACTCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TACCTGCGCTATGTGGTGGCCGGTGATCTGGGTAAAG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GGGCAATTACGTTACTACCTTCATCGAAGCCTAACCA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGATCGTAGATGTGATTCGGGTTACAGTTGCCATCGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAGGTGGTCAAACCCTCAATTTTTTCTTGGAGTTCTGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TAAACTCCCGAAATTCTTCGCTCATTTGGCGCAAGAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCGTATTGCGCTGAATCCTATCAGCCAAAACCTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AGGTGAAAAAAGGTACATTACAGGGTACGAGTGGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAATAGTGTTGGCAGATGTTGGCAGGCTGCCGAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGTTGAGAGGTGGTTTACCCACAAATCCGCATACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AACAACGACTCAACCATTTGCTTAGACACTTTCATGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGCCCCCGTCGTCAGCTTTGAGCCGGGGGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCCGTTGTGGACGACGCCATGCCGGGACTACTCGGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGTAGGCCAGATTGTACGCCAGTCCCGTTAACGGTAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGATTGGGTTCCGTTCGACATTGTGTCGAACGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTCCTTTCGCCATAAGCTAAGTAACTTTTTAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTTGGAGCGGTTAGTTTACGTATGCGGATTTGTGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACGCTCAAGACCCGCCCCCTGATGGACGATCAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGCGCGTCGTCTACAGCCGTTAGGCTGACCGTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGATGGCCGCTATTGGGGTAAGCAGCTACAATACATA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTATTGCAGGAATGTGCCTCGTCATTATCTTATTAGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTCGTTTACCAGGGCAATGTACTCTGTCAGGTACTC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTGTTGTCACCACATATCAGCCCAATGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCAACTGAAGCGATACGGCCATGCGTTGATGCCTCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAATCCAGTGGCACAGGTAGCAGGTCGCGCTTTTCGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ATGACTCGGTTTTTCAGGTCTCTGATTTGCATGGCTTG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGTGATTTAGTAATCTCAATCCCGTAGTGTTCACT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACCGTCTGACAGGTTGCCAACGAGCGCGGCTTAGATGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCCAATTCAGGGATACCTGGGTGCAACTCTGCCAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCAGAACGTGTAATTTAGCCGTATGTCCAAACGAACA


>NZ_CP014263|4|1|3424944-3429101|CRT
GTTTCAATCCTGCTTATTAGTGGATTAGCTCTCGAAT	GCGATGTCGAAGCTACCCGCCGTGCTTGAAGCGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	TTTCGGCGGCTTTGCGTTCGATGATACCCACGAAGAGCGTAG
GTTTCAATCCTGCTTATCAGTGGGTTAGCTCTCGAAT	ATGTCCTCGGCGCACATTATTACCTCGGCGCGGCAGT
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GCGCATGTCGGCCTCCGGGTTTGCCAGCAACTGGTACA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCAGCAGCCCCGGCATTCGGGCCATTTCCATTCT
GTTTCAATCCTGCTTATCAATGGATTAGCTCTCGAAT	ATATGCTTATTGACTATATCCGAAATCCCGATTTAGC
GTTTCAATCCTGCTTTTCAGTGGATTAGCTCTCGAAT	CCTGCTGGCAGTGGTGGCCGGTGGCTTAATCCTTTAC
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGGAGCAATACCGAGAGTTTACCATCGGGCTATAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGGTAGTTCCGTAATGCACACAAGCCGACAGAAAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAAACCAAAGCCGGGGCCAGCATCGACGTAGACGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCCACGTGGTTGCGCGGCAAGTACGATAACGATTA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AACCGACCGCCGAGGGCCGGGCCTACGAGGAAAAAAT
GTTTCAATCCTGCTTTTGCTCTCGAATGTCGCAGGGC	GTCATGGACAAACTCGCTCAGTACAC
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCTTTGCCCGAAAAAAACACGTACAGAATACTTTCGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTCGATTGAGCCGCTGGTTAAGTTTGTGGAAGAGTA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GGCCTACGCCAAGAGTGCACGCAGTTCGGGCATCGA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGATTCGGGATACCAACGAAAGCCACGGCGGTACGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	AACCGGAACAGCTTCGTGCAGGTTGAAGCCCATGA
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	ATATACATTTGTGTCAACAAGCCGGGAAACATTCGAG
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	AAGTCCAGCAGGGCCAACAGATCCACGCGCTGCTCAT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CTTCCAGATCGTGGGGAGCCTCTTTGGTGTCTACTT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CGTGTTTGCCGGTTCTTTGTACGTAGGGGCTTCACCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGCGGCATCACCAATTGGCGCAGCGGGTAACAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTGTTCCGTCACCCTTCGCGCCCCACAACTGTACGC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTTTTTCAGGAAAGCATGTCGTCTTCCTGTTGCAC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGCGCAGGCGGCAATGGAGCGGGCCACCGCTCCGGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTACACCGAACGCTTCGTAATAGTCGCATACTCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TACCTGCGCTATGTGGTGGCCGGTGATCTGGGTAAAG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GGGCAATTACGTTACTACCTTCATCGAAGCCTAACCA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGATCGTAGATGTGATTCGGGTTACAGTTGCCATCGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAGGTGGTCAAACCCTCAATTTTTTCTTGGAGTTCTGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TAAACTCCCGAAATTCTTCGCTCATTTGGCGCAAGAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCGTATTGCGCTGAATCCTATCAGCCAAAACCTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AGGTGAAAAAAGGTACATTACAGGGTACGAGTGGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAATAGTGTTGGCAGATGTTGGCAGGCTGCCGAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGTTGAGAGGTGGTTTACCCACAAATCCGCATACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AACAACGACTCAACCATTTGCTTAGACACTTTCATGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGCCCCCGTCGTCAGCTTTGAGCCGGGGGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCCGTTGTGGACGACGCCATGCCGGGACTACTCGGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGTAGGCCAGATTGTACGCCAGTCCCGTTAACGGTAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGATTGGGTTCCGTTCGACATTGTGTCGAACGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTCCTTTCGCCATAAGCTAAGTAACTTTTTAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTTGGAGCGGTTAGTTTACGTATGCGGATTTGTGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACGCTCAAGACCCGCCCCCTGATGGACGATCAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGCGCGTCGTCTACAGCCGTTAGGCTGACCGTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGATGGCCGCTATTGGGGTAAGCAGCTACAATACATA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTATTGCAGGAATGTGCCTCGTCATTATCTTATTAGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTCGTTTACCAGGGCAATGTACTCTGTCAGGTACTC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTGTTGTCACCACATATCAGCCCAATGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCAACTGAAGCGATACGGCCATGCGTTGATGCCTCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAATCCAGTGGCACAGGTAGCAGGTCGCGCTTTTCGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ATGACTCGGTTTTTCAGGTCTCTGATTTGCATGGCTTG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGTGATTTAGTAATCTCAATCCCGTAGTGTTCACT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACCGTCTGACAGGTTGCCAACGAGCGCGGCTTAGATGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCCAATTCAGGGATACCTGGGTGCAACTCTGCCAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCAGAACGTGTAATTTAGCCGTATGTCCAAACGAACA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT

>NZ_CP014263|4|1|3425095-3425797|PILER-CR
GTTTCAATCCTGCTTATCAGTGGGTTAGCTCTCGAAT	ATGTCCTCGGCGCACATTATTACCTCGGCGCGGCAGT
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GCGCATGTCGGCCTCCGGGTTTGCCAGCAACTGGTACA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCAGCAGCCCCGGCATTCGGGCCATTTCCATTCT
GTTTCAATCCTGCTTATCAATGGATTAGCTCTCGAAT	ATATGCTTATTGACTATATCCGAAATCCCGATTTAGC
GTTTCAATCCTGCTTTTCAGTGGATTAGCTCTCGAAT	CCTGCTGGCAGTGGTGGCCGGTGGCTTAATCCTTTAC
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGGAGCAATACCGAGAGTTTACCATCGGGCTATAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGGTAGTTCCGTAATGCACACAAGCCGACAGAAAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAAACCAAAGCCGGGGCCAGCATCGACGTAGACGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCCACGTGGTTGCGCGGCAAGTACGATAACGATTA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAACCGACCGCCGAGGGCCGGGCCTACGAGGAAAAAATGTTTCAATCCTGCTTTTGCTCTCGAATGTCGCAGGGCGTCATGGACAAACTCGCTCAGTACACGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCTTTGCCCGAAAAAAACACGTACAGAATACTTTCGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTCGATTGAGCCGCTGGTTAAGTTTGTGGAAGAGTA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GGCCTACGCCAAGAGTGCACGCAGTTCGGGCATCGA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGATTCGGGATACCAACGAAAGCCACGGCGGTACGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	AACCGGAACAGCTTCGTGCAGGTTGAAGCCCATGA
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	ATATACATTTGTGTCAACAAGCCGGGAAACATTCGAG
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	AAGTCCAGCAGGGCCAACAGATCCACGCGCTGCTCAT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CTTCCAGATCGTGGGGAGCCTCTTTGGTGTCTACTT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CGTGTTTGCCGGTTCTTTGTACGTAGGGGCTTCACCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGCGGCATCACCAATTGGCGCAGCGGGTAACAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTGTTCCGTCACCCTTCGCGCCCCACAACTGTACGC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTTTTTCAGGAAAGCATGTCGTCTTCCTGTTGCAC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGCGCAGGCGGCAATGGAGCGGGCCACCGCTCCGGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTACACCGAACGCTTCGTAATAGTCGCATACTCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TACCTGCGCTATGTGGTGGCCGGTGATCTGGGTAAAG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GGGCAATTACGTTACTACCTTCATCGAAGCCTAACCA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGATCGTAGATGTGATTCGGGTTACAGTTGCCATCGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAGGTGGTCAAACCCTCAATTTTTTCTTGGAGTTCTGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TAAACTCCCGAAATTCTTCGCTCATTTGGCGCAAGAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCGTATTGCGCTGAATCCTATCAGCCAAAACCTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AGGTGAAAAAAGGTACATTACAGGGTACGAGTGGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAATAGTGTTGGCAGATGTTGGCAGGCTGCCGAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGTTGAGAGGTGGTTTACCCACAAATCCGCATACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AACAACGACTCAACCATTTGCTTAGACACTTTCATGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGCCCCCGTCGTCAGCTTTGAGCCGGGGGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCCGTTGTGGACGACGCCATGCCGGGACTACTCGGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGTAGGCCAGATTGTACGCCAGTCCCGTTAACGGTAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGATTGGGTTCCGTTCGACATTGTGTCGAACGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTCCTTTCGCCATAAGCTAAGTAACTTTTTAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTTGGAGCGGTTAGTTTACGTATGCGGATTTGTGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACGCTCAAGACCCGCCCCCTGATGGACGATCAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGCGCGTCGTCTACAGCCGTTAGGCTGACCGTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGATGGCCGCTATTGGGGTAAGCAGCTACAATACATA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTATTGCAGGAATGTGCCTCGTCATTATCTTATTAGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTCGTTTACCAGGGCAATGTACTCTGTCAGGTACTC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTGTTGTCACCACATATCAGCCCAATGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCAACTGAAGCGATACGGCCATGCGTTGATGCCTCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAATCCAGTGGCACAGGTAGCAGGTCGCGCTTTTCGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ATGACTCGGTTTTTCAGGTCTCTGATTTGCATGGCTTG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGTGATTTAGTAATCTCAATCCCGTAGTGTTCACT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACCGTCTGACAGGTTGCCAACGAGCGCGGCTTAGATGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCCAATTCAGGGATACCTGGGTGCAACTCTGCCAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCAGAACGTGTAATTTAGCCGTATGTCCAAACGAACA


>NZ_CP014263|4|2|3425898-3429101|PILER-CR
	ATGTCCTCGGCGCACATTATTACCTCGGCGCGGCAGT
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GCGCATGTCGGCCTCCGGGTTTGCCAGCAACTGGTACA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCAGCAGCCCCGGCATTCGGGCCATTTCCATTCT
GTTTCAATCCTGCTTATCAATGGATTAGCTCTCGAAT	ATATGCTTATTGACTATATCCGAAATCCCGATTTAGC
GTTTCAATCCTGCTTTTCAGTGGATTAGCTCTCGAAT	CCTGCTGGCAGTGGTGGCCGGTGGCTTAATCCTTTAC
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGGAGCAATACCGAGAGTTTACCATCGGGCTATAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGGTAGTTCCGTAATGCACACAAGCCGACAGAAAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAAACCAAAGCCGGGGCCAGCATCGACGTAGACGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCCACGTGGTTGCGCGGCAAGTACGATAACGATTA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAACCGACCGCCGAGGGCCGGGCCTACGAGGAAAAAATGTTTCAATCCTGCTTTTGCTCTCGAATGTCGCAGGGCGTCATGGACAAACTCGCTCAGTACACGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCTTTGCCCGAAAAAAACACGTACAGAATACTTTCGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTCGATTGAGCCGCTGGTTAAGTTTGTGGAAGAGTA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GGCCTACGCCAAGAGTGCACGCAGTTCGGGCATCGA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGATTCGGGATACCAACGAAAGCCACGGCGGTACGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	AACCGGAACAGCTTCGTGCAGGTTGAAGCCCATGA
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	ATATACATTTGTGTCAACAAGCCGGGAAACATTCGAG
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	AAGTCCAGCAGGGCCAACAGATCCACGCGCTGCTCAT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CTTCCAGATCGTGGGGAGCCTCTTTGGTGTCTACTT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CGTGTTTGCCGGTTCTTTGTACGTAGGGGCTTCACCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGCGGCATCACCAATTGGCGCAGCGGGTAACAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTGTTCCGTCACCCTTCGCGCCCCACAACTGTACGC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTTTTTCAGGAAAGCATGTCGTCTTCCTGTTGCAC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGCGCAGGCGGCAATGGAGCGGGCCACCGCTCCGGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTACACCGAACGCTTCGTAATAGTCGCATACTCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TACCTGCGCTATGTGGTGGCCGGTGATCTGGGTAAAG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GGGCAATTACGTTACTACCTTCATCGAAGCCTAACCA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGATCGTAGATGTGATTCGGGTTACAGTTGCCATCGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAGGTGGTCAAACCCTCAATTTTTTCTTGGAGTTCTGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TAAACTCCCGAAATTCTTCGCTCATTTGGCGCAAGAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCGTATTGCGCTGAATCCTATCAGCCAAAACCTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AGGTGAAAAAAGGTACATTACAGGGTACGAGTGGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAATAGTGTTGGCAGATGTTGGCAGGCTGCCGAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGTTGAGAGGTGGTTTACCCACAAATCCGCATACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AACAACGACTCAACCATTTGCTTAGACACTTTCATGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGCCCCCGTCGTCAGCTTTGAGCCGGGGGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCCGTTGTGGACGACGCCATGCCGGGACTACTCGGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGTAGGCCAGATTGTACGCCAGTCCCGTTAACGGTAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGATTGGGTTCCGTTCGACATTGTGTCGAACGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTCCTTTCGCCATAAGCTAAGTAACTTTTTAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTTGGAGCGGTTAGTTTACGTATGCGGATTTGTGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACGCTCAAGACCCGCCCCCTGATGGACGATCAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGCGCGTCGTCTACAGCCGTTAGGCTGACCGTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGATGGCCGCTATTGGGGTAAGCAGCTACAATACATA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTATTGCAGGAATGTGCCTCGTCATTATCTTATTAGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTCGTTTACCAGGGCAATGTACTCTGTCAGGTACTC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTGTTGTCACCACATATCAGCCCAATGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCAACTGAAGCGATACGGCCATGCGTTGATGCCTCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAATCCAGTGGCACAGGTAGCAGGTCGCGCTTTTCGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ATGACTCGGTTTTTCAGGTCTCTGATTTGCATGGCTTG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGTGATTTAGTAATCTCAATCCCGTAGTGTTCACT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACCGTCTGACAGGTTGCCAACGAGCGCGGCTTAGATGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCCAATTCAGGGATACCTGGGTGCAACTCTGCCAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCAGAACGTGTAATTTAGCCGTATGTCCAAACGAACA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT

>NZ_CP014263|4|5|3425898-3429101|CRISPRCasFinder
	GCGATGTCGAAGCTACCCGCCGTGCTTGAAGCGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	TTTCGGCGGCTTTGCGTTCGATGATACCCACGAAGAGCGTAG
GTTTCAATCCTGCTTATCAGTGGGTTAGCTCTCGAAT	ATGTCCTCGGCGCACATTATTACCTCGGCGCGGCAGT
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GCGCATGTCGGCCTCCGGGTTTGCCAGCAACTGGTACA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCAGCAGCCCCGGCATTCGGGCCATTTCCATTCT
GTTTCAATCCTGCTTATCAATGGATTAGCTCTCGAAT	ATATGCTTATTGACTATATCCGAAATCCCGATTTAGC
GTTTCAATCCTGCTTTTCAGTGGATTAGCTCTCGAAT	CCTGCTGGCAGTGGTGGCCGGTGGCTTAATCCTTTAC
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGGAGCAATACCGAGAGTTTACCATCGGGCTATAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGGTAGTTCCGTAATGCACACAAGCCGACAGAAAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAAACCAAAGCCGGGGCCAGCATCGACGTAGACGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCCACGTGGTTGCGCGGCAAGTACGATAACGATTA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAATAACCGACCGCCGAGGGCCGGGCCTACGAGGAAAAAATGTTTCAATCCTGCTTTTGCTCTCGAATGTCGCAGGGCGTCATGGACAAACTCGCTCAGTACACGTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CGTCTTTGCCCGAAAAAAACACGTACAGAATACTTTCGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTCGATTGAGCCGCTGGTTAAGTTTGTGGAAGAGTA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	GGCCTACGCCAAGAGTGCACGCAGTTCGGGCATCGA
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	CTGATTCGGGATACCAACGAAAGCCACGGCGGTACGGG
GTTTCAATCCTGCTTATCAGTGGATTAGCTCTCGAAT	AACCGGAACAGCTTCGTGCAGGTTGAAGCCCATGA
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	ATATACATTTGTGTCAACAAGCCGGGAAACATTCGAG
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	AAGTCCAGCAGGGCCAACAGATCCACGCGCTGCTCAT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CTTCCAGATCGTGGGGAGCCTCTTTGGTGTCTACTT
GTTTCAATCCTACTTTTCAATGGATTAGCTCTCGAAT	CGTGTTTGCCGGTTCTTTGTACGTAGGGGCTTCACCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGCGGCATCACCAATTGGCGCAGCGGGTAACAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTGTTCCGTCACCCTTCGCGCCCCACAACTGTACGC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTTTTTCAGGAAAGCATGTCGTCTTCCTGTTGCAC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGCGCAGGCGGCAATGGAGCGGGCCACCGCTCCGGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTACACCGAACGCTTCGTAATAGTCGCATACTCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TACCTGCGCTATGTGGTGGCCGGTGATCTGGGTAAAG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GGGCAATTACGTTACTACCTTCATCGAAGCCTAACCA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGATCGTAGATGTGATTCGGGTTACAGTTGCCATCGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAGGTGGTCAAACCCTCAATTTTTTCTTGGAGTTCTGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TAAACTCCCGAAATTCTTCGCTCATTTGGCGCAAGAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCGGCGTATTGCGCTGAATCCTATCAGCCAAAACCTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AGGTGAAAAAAGGTACATTACAGGGTACGAGTGGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAAATAGTGTTGGCAGATGTTGGCAGGCTGCCGAAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGTTGAGAGGTGGTTTACCCACAAATCCGCATACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AACAACGACTCAACCATTTGCTTAGACACTTTCATGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CTGGCCCCCGTCGTCAGCTTTGAGCCGGGGGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCCGTTGTGGACGACGCCATGCCGGGACTACTCGGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGTAGGCCAGATTGTACGCCAGTCCCGTTAACGGTAT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGATTGGGTTCCGTTCGACATTGTGTCGAACGACG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTCCTTTCGCCATAAGCTAAGTAACTTTTTAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTTGGAGCGGTTAGTTTACGTATGCGGATTTGTGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACGCTCAAGACCCGCCCCCTGATGGACGATCAGGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	AAGCGCGTCGTCTACAGCCGTTAGGCTGACCGTGT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CGATGGCCGCTATTGGGGTAAGCAGCTACAATACATA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTATTGCAGGAATGTGCCTCGTCATTATCTTATTAGA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	GTCGTTTACCAGGGCAATGTACTCTGTCAGGTACTC
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TTTCTTGTTGTCACCACATATCAGCCCAATGGCGAAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCAACTGAAGCGATACGGCCATGCGTTGATGCCTCG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CAATCCAGTGGCACAGGTAGCAGGTCGCGCTTTTCGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ATGACTCGGTTTTTCAGGTCTCTGATTTGCATGGCTTG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TGGTGATTTAGTAATCTCAATCCCGTAGTGTTCACT
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	ACCGTCTGACAGGTTGCCAACGAGCGCGGCTTAGATGG
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	CCCAATTCAGGGATACCTGGGTGCAACTCTGCCAA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT	TCAGAACGTGTAATTTAGCCGTATGTCCAAACGAACA
GTTTCAATCCTGCTTTTCAATGGATTAGCTCTCGAAT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014263.1|WP_077131888.1|3431357_3432092_-|CRISPR-associated-endonuclease-Cas6	cas6	cls000004_cas6_CAS-I:CAS-III	gnl|CDD|379957
NZ_CP014263.1|WP_077131879.1|3416755_3417208_+|DUF4174-domain-containing-protein	unknown	unknown	gnl|CDD|379363
NZ_CP014263.1|WP_077131882.1|3420312_3421170_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077131892.1|3437995_3438208_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077131891.1|3436010_3437792_-|hypothetical-protein	cas8b8	cls000685_cas8b8_CAS-I-B	unknown
NZ_CP014263.1|WP_077134011.1|3432100_3434392_-|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl|CDD|224124
NZ_CP014263.1|WP_077131890.1|3435121_3436021_-|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	cas7	cd09687_cas7_CAS-I-B	gnl|CDD|187818
NZ_CP014263.1|WP_077131885.1|3429300_3429888_-|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl|CDD|187768
NZ_CP014263.1|WP_077134009.1|3421375_3421900_-|DUF2911-domain-containing-protein	unknown	unknown	gnl|CDD|378565
NZ_CP014263.1|WP_083732865.1|3424167_3424590_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077131877.1|3416140_3416350_+|membrane-protein-insertion-efficiency-factor-YidD	unknown	unknown	gnl|CDD|376620
NZ_CP014263.1|WP_077131884.1|3423885_3424128_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077131889.1|3434396_3435110_-|CRISPR-associated-protein-Cas5	cas5	cd09693_cas5_CAS-I	gnl|CDD|273860
NZ_CP014263.1|WP_077131880.1|3417343_3419296_-|sialate-O-acetylesterase	unknown	unknown	gnl|CDD|377084
NZ_CP014263.1|WP_077131894.1|3438505_3440317_-|gamma-glutamyltransferase	unknown	unknown	gnl|CDD|223482
NZ_CP014263.1|WP_077131881.1|3419369_3420266_+|SDR-family-oxidoreductase	unknown	unknown	gnl|CDD|187578
NZ_CP014263.1|WP_077131887.1|3430218_3431295_-|CRISPR-associated-endonuclease-Cas1	cas1	pfam01867_cas1_CAS-I:CAS-II:CAS-III	gnl|CDD|187766
NZ_CP014263.1|WP_077131886.1|3429931_3430222_-|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl|CDD|187856
NZ_CP014263.1|WP_077131878.1|3416366_3416744_+|co-chaperone-GroES	unknown	unknown	gnl|CDD|238197
NZ_CP014263.1|WP_077131883.1|3422054_3423875_+|acyl-CoA-dehydrogenase	unknown	unknown	gnl|CDD|173842

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP014263.1|WP_077131890.1|3435121_3436021_-|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	cas7	cd09687_cas7_CAS-I-B	1.3e-67	222.9	0.0
NZ_CP014263.1|WP_077131887.1|3430218_3431295_-|CRISPR-associated-endonuclease-Cas1	cas1	pfam01867_cas1_CAS-I:CAS-II:CAS-III	1.3e-76	252.3	0.0
NZ_CP014263.1|WP_077131891.1|3436010_3437792_-|hypothetical-protein	cas8b8	cls000685_cas8b8_CAS-I-B	0	1166.1	8.5
NZ_CP014263.1|WP_077131886.1|3429931_3430222_-|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	5.8e-22	72.5	0.1
NZ_CP014263.1|WP_077131888.1|3431357_3432092_-|CRISPR-associated-endonuclease-Cas6	cas6	cls000004_cas6_CAS-I:CAS-III	6.2e-72	236.4	0.0
NZ_CP014263.1|WP_077131885.1|3429300_3429888_-|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	3.4e-32	106.8	0.1
NZ_CP014263.1|WP_077131889.1|3434396_3435110_-|CRISPR-associated-protein-Cas5	cas5	cd09693_cas5_CAS-I	2.3e-16	54.9	0.0
NZ_CP014263.1|WP_077134011.1|3432100_3434392_-|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	4.5e-77	254.6	2.8

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP014263.1|WP_077134011.1|3432100_3434392_-|CRISPR-associated-helicase/endonuclease-Cas3	gnl|CDD|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	1.36139e-59
NZ_CP014263.1|WP_077131879.1|3416755_3417208_+|DUF4174-domain-containing-protein	gnl|CDD|379363	pfam13778, DUF4174, Domain of unknown function (DUF4174). This domain of unknown function is found in a putative tumor suppressor gene and in a ligand for the the urokinase-type plasminogen activator receptor, which plays a role in cellular migration and adhesion.	1.085e-28
NZ_CP014263.1|WP_077131894.1|3438505_3440317_-|gamma-glutamyltransferase	gnl|CDD|223482	COG0405, Ggt, Gamma-glutamyltransferase [Amino acid transport and metabolism].	0
NZ_CP014263.1|WP_077131878.1|3416366_3416744_+|co-chaperone-GroES	gnl|CDD|238197	cd00320, cpn10, Chaperonin 10 Kd subunit (cpn10 or GroES); Cpn10 cooperates with chaperonin 60 (cpn60 or GroEL), an ATPase, to assist the folding and assembly of proteins and is found in eubacterial cytosol, as well as in the matrix of mitochondria and chloroplasts. It forms heptameric rings with a dome-like structure, forming a lid to the large cavity of the tetradecameric cpn60 cylinder and thereby tightly regulating release and binding of proteins to the cpn60 surface.	4.06074e-18
NZ_CP014263.1|WP_077131890.1|3435121_3436021_-|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	gnl|CDD|187818	cd09687, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Cst2/DevR family.	3.04665e-68
NZ_CP014263.1|WP_077131885.1|3429300_3429888_-|CRISPR-associated-protein-Cas4	gnl|CDD|187768	cd09637, Cas4_I-A_I-B_I-C_I-D_II-B, CRISPR/Cas system-associated protein Cas4. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas4 is RecB-like nuclease with three-cysteine C-terminal cluster.	3.15713e-24
NZ_CP014263.1|WP_077134009.1|3421375_3421900_-|DUF2911-domain-containing-protein	gnl|CDD|378565	pfam11138, DUF2911, Protein of unknown function (DUF2911). This bacterial family of proteins has no known function.	2.06354e-62
NZ_CP014263.1|WP_077131889.1|3434396_3435110_-|CRISPR-associated-protein-Cas5	gnl|CDD|273860	TIGR01895, conserved_hypothetical_protein, CRISPR-associated protein Cas5, subtype I-B/TNEAP. CRISPR is a term for Clustered Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This family is represented by TM1800 from Thermotoga maritima. It is related to TIGR01868 (CRISPR-associated protein, CT1976 family).	1.05311e-13
NZ_CP014263.1|WP_077131877.1|3416140_3416350_+|membrane-protein-insertion-efficiency-factor-YidD	gnl|CDD|376620	pfam01809, Haemolytic, Haemolytic domain. This domain has haemolytic activity. It is found in short (73-103 amino acid) proteins and contains three conserved cysteine residues.	4.91951e-39
NZ_CP014263.1|WP_077131880.1|3417343_3419296_-|sialate-O-acetylesterase	gnl|CDD|377084	pfam03629, SASA, Carbohydrate esterase, sialic acid-specific acetylesterase. The catalytic triad of this esterase enzyme comprises residues Ser127, His403 and Asp391 in UniProtKB:P70665.	3.17036e-10
NZ_CP014263.1|WP_077131886.1|3429931_3430222_-|CRISPR-associated-endonuclease-Cas2	gnl|CDD|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	2.7002e-20
NZ_CP014263.1|WP_077131887.1|3430218_3431295_-|CRISPR-associated-endonuclease-Cas1	gnl|CDD|187766	cd09634, Cas1_I-II-III, CRISPR/Cas system-associated protein Cas1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas1 is the most universal CRISPR system protein thought to be involved in spacer integration; Cas1 is metal-dependent deoxyribonuclease, also binds RNA; Shown to possess a unique fold consisting of a N-terminal beta-strand domain and a C-terminal alpha-helical domain.	2.8013e-86
NZ_CP014263.1|WP_077131881.1|3419369_3420266_+|SDR-family-oxidoreductase	gnl|CDD|187578	cd05269, TMR_SDR_a, triphenylmethane reductase (TMR)-like proteins, NMRa-like, atypical (a) SDRs. TMR is an atypical NADP-binding protein of the SDR family. It lacks the active site residues of the SDRs but has a glycine rich NAD(P)-binding motif that matches the extended SDRs. Proteins in this subgroup however, are more similar in length to the classical SDRs. TMR was identified as a reducer of triphenylmethane dyes, important environmental pollutants. This subgroup also includes Escherichia coli NADPH-dependent quinine oxidoreductase (QOR2), which catalyzes two-electron reduction of quinone; but is unlikely to play a major role in protecting against quinone cytotoxicity. Atypical SDRs are distinct from classical SDRs. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	6.32898e-87
NZ_CP014263.1|WP_077131883.1|3422054_3423875_+|acyl-CoA-dehydrogenase	gnl|CDD|173842	cd01153, ACAD_fadE5, Putative acyl-CoA dehydrogenases similar to fadE5. Putative acyl-CoA dehydrogenase (ACAD). Mitochondrial acyl-CoA dehydrogenases (ACAD) catalyze the alpha,beta dehydrogenation of the corresponding trans-enoyl-CoA by FAD, which becomes reduced. The reduced form of ACAD is reoxidized in the oxidative half-reaction by electron-transferring flavoprotein (ETF), from which the electrons are transferred to the mitochondrial respiratory chain coupled with ATP synthesis. The ACD family includes the eukaryotic beta-oxidation, as well as amino acid catabolism enzymes. These enzymes share high sequence similarity, but differ in their substrate specificities. The mitochondrial ACD's are generally homotetramers and have an active site glutamate at a conserved position.	3.68282e-146
NZ_CP014263.1|WP_077131888.1|3431357_3432092_-|CRISPR-associated-endonuclease-Cas6	gnl|CDD|379957	pfam17262, DUF5328, Family of unknown function (DUF5328). This family of unknown function can be found in Bacteria and Archaea. Some of the proteins in this family are annotated in UniProt as putative DNA repair proteins.	4.3014e-43

Protein sequences

>NZ_CP014263.1|WP_083732865.1|3424167_3424590_+|hypothetical-protein
MNTEQLINLIQAAQTPDQIREANRLAAAYLKASEGLDSYEKQAVQRAKSDALNRFLDEVEFEQQETLRFLALNGKQYDLNEWLTPMEYARKYNLRSVNNVTNWMIRGVIPPADIVDVPELNGLRLVRDRVYKEIPQGMGS
>NZ_CP014263.1|WP_077131884.1|3423885_3424128_-|hypothetical-protein
MFTFLPVFCLPCRRLVELIDYQVGTAKNLLREVVVAVLTAVATYMVVHALQPANPLKNKTCSVKCIRLANHNPVHFTEHA
>NZ_CP014263.1|WP_077131883.1|3422054_3423875_+|acyl-CoA-dehydrogenase
MATTYFSKRNLHFLLHEVFKAEELTQYEYFSAHDRETFNLVLDSATYIADTLMHPYLKEVDKNQPELKDGQVTVHPKVKEFMQAMGDAGLIGAGFSFEHGGQQLPEMISSCVGFILMAANNGMMYTGLSSGAAHLITSFGSPELSEFYVPNMLSGKWQGTMALTEPQAGSSLSDVTTSATPLTDGESVPGSYKIKGQKVFISAGDHDAVDNVVHLMLARIDGAPKGTKGISLFVVPKYRPDGNNGFVDNDVQSTGVYHKMGQKGVPAMHLTMGSNDNTIGYIVGEPHQGLPYMFQMMNEARIGVGMTAAAIATAAYHAAVQYARERPQSRRLNEKNLLDAPQTPIINHPDVRRMLLFQKAVTEGSLSVLIEAARLYDISKVAEGDDKDNAFLLLDLLMPVAKTYPSEMGVQSVSQSLQTFGGYGFTEDFPVEQLYRDIRITPIYEGTTGIQAQDLLGRKMTMKGGKAPQLLFAEMGKTIAEASMFDDLKPYAEQLNGEMKRIQEVFSALLPHAMKGDTERYLADATLFLELFGIVVVAWQWLKQAIVAKHALLTQNPQGDDLTFYEGKLHTMKFFFHYEVPKTLGLAVRLKDPEVLTIVSEKELAL
>NZ_CP014263.1|WP_077134009.1|3421375_3421900_-|DUF2911-domain-containing-protein
MKKLLFVFSFLFAMVSLAQAQDKKPPMSPRITAESPDKSIKVAYGQPSKRGRVVFGEGGLEKYGKVWRTGANEATEITFANDVMFGGKMVKAGTYTLYTIPGEKEWTVLLNSTLGQWGAYDYEKIKSGDVASVKVPVSMNKTAIEKLTITPANSSLTIAWDNMTVSVPVTKHGS
>NZ_CP014263.1|WP_077131882.1|3420312_3421170_-|hypothetical-protein
MMKRYLLYSCLALAALPAVGQDMADYYRLPDRSRQLDRLTMRYGGPQIRDRWYVSFDAFVRTDRAKLDNSLNGLIESDRVTKLDWSAVVGWSARERWAIEAGYARMPIHTQVSVSNGRSPLVYRYTNSHNAFMLRGKRLLASTSGPWLRSGFWLSGGMWLVPNNGQREGQFSLIGYRRNETVDTLRLNSQTNVNGRATAMAELGAEYNVRLSNNVDLGFTVRKFWGLGTSLTTDVAYTINNTLAQQAQLRGTGSGMSYGVSLRYTLSLRRKQPDVLEVQGRQRIR
>NZ_CP014263.1|WP_077131881.1|3419369_3420266_+|SDR-family-oxidoreductase
MLPSTAERILITGASGNVGLETLRALVKHPHKSQIELLAGTRSPETDMRVIPIQPDRYVLLDFTDPATFDAALSGVRRVLLVRPPQLSDANRYFRPFVEAMKRAGVQHVVFLSLQGVENNPVTPHYTIEKLIVEAGLPFTFLRPSFFMQNLSTTHRDEIRSRNEIFIPAGNGRTSFVDVRDIGAVAALVLTDTTGNHLNRGYELTGSEALTYSEVAQMLTQVLGRKISYRNPSVVRFIWRKWLTEKNPLGFTLVMVALYTVSKLGKAARTTSDLERLLKRPPIKFRQFAMDTKAAWLS
>NZ_CP014263.1|WP_077131880.1|3417343_3419296_-|sialate-O-acetylesterase
MKSFCYRWLFIFLAMAQPVLADVRLPHVFGSHMVLQRRKPLPIWGWADANERVTVLLNKQTKTIKAGKDGRWQLTLDPMEAGGPYDLTVKGSKNELVLTDVLLGEVWVCSGQSNMEWPLRQATNANKEINAANYPQIRQLLVKKAISLTPKDDIEGEWAVCTPGTAPAFTAVGYFFARQLQQELNVPIGLINTSWGGTHSETWTSRQAMASDPELAKAVANLPADLEQMRQSGQERIRQLIQTVQGGILPTPADELAWANPDFNAADWKTIAMPGDWEWRGLPVFDGVVWLRREVTLPANTDLLNPQLLFGAVDDADSTFVNGQFVGTTNGRTKPRLYELPNGLLKPGRNVIVVRVKDTGGSGGLMGDPEAMKLTFGTTELPLAGSWQYRIAQAFPSSYTAGPNTYATLLFNAMLKPLIPYAIAGTIWYQGESNAGRAHQYRRAFPLLIQDWRQHWGYEFPFLFVQLASYNSANGDSRKGSTWGELREAQTLTLQLPNTGMAVTSDIGEANDIHPRNKQDVGKRLAAEAMRVAYQKPGVSAGPLFEKMTVDGNRAVLLFRNTGSGLSVKDRYGYLKGFELAGTDQQFHYAKAEIQGNTVVVYCDAVAAPVAVRYGWADDNGDVNLYNREGFPAVPFRTDTWKGVTEGKTF
>NZ_CP014263.1|WP_077131879.1|3416755_3417208_+|DUF4174-domain-containing-protein
MQRRWFLLVAVLILGLTLVMESVANQRKSLKAILSEKKDHRRVLLLYGRDGSSGGPGQRLLIEQQENLNEHRNGLAERDLDVIVLIASEVSEPDRQFLMHEYHLQPSEEFIGWLIGKDGGLKHTYKKPVDAAELFGLIDTMPMRKQEMKQ
>NZ_CP014263.1|WP_077131878.1|3416366_3416744_+|co-chaperone-GroES
MIGISADNKLKRLIVVGDRVLIKPKDPTDRTASGLYLPPTVQEKEQVQSGYVIKAGPGYPIPVATEDEPWKETEEKVKYMPLQAQEGDLALYLQRNAIDLQYEGEQYVIVPQASILMLERSEDLA
>NZ_CP014263.1|WP_077131877.1|3416140_3416350_+|membrane-protein-insertion-efficiency-factor-YidD
MKHLLIGLVRLYQAILSPWLPNACRYTPTCSQYAIDAIRKYGAVRGGWLGLKRIGRCHPWGGHGYDPVP
>NZ_CP014263.1|WP_077131885.1|3429300_3429888_-|CRISPR-associated-protein-Cas4
MTLTPSHIIEYLFCPRFTYFEYVLGIPQYEDKNYKVMRGRHLHDERLERNKDYLRRRLGRPGAPVVEKLVDQYLTNAFLRGVVDEVLAFGDESMAPLDYKFAEYKDKIFSTYQTQLYCYAWLIEDNFDRRVDRGFLVYTRSNNRVVEVPITDENKADVRRAAEAIFSIIDRNFFPKATKAKARCVTCTYRNVCIK
>NZ_CP014263.1|WP_077131886.1|3429931_3430222_-|CRISPR-associated-endonuclease-Cas2
MTIWVLYDIVNDKARSKAAKRCQQAGLYRVQFSCFLGTLTQNQKDTLQLQLEELINEETDKVYIFPMSRSELQQTVLLGQAFDRKLVTDEIRALFF
>NZ_CP014263.1|WP_077131887.1|3430218_3431295_-|CRISPR-associated-endonuclease-Cas1
MQLHITTYGTYLHVKDSMFDVRRKGDDGRVLSATYSAEKVTHILLATGTSLSTDAVKLAMRHNVDIVFLERDGDPMGRVWHAKLGSTTKIRKRQLEVSLGAEGLRWVRTWLLAKLDNQAGFIRSLKKHRLQHSAYLDDKLARLDALSVSISTLDGARVADVADTLRGLEGTAGRLYFETLSYVLPADYQFNGRSSRPAHDAFNAFLNYAYGMLYGKVEKTLMLAGLDPYVGFLHRDDYNQLSMVYDFIEPYRGWADEVVFRLFSAKKVNKSHVDAVSGGRNGGAKAGESTPGESTPGVSLNAEGKPLLVNAFNEFMDNDPIRYRGRNLVRSHCIQLDAHQFANELIGKTGGMPELTML
>NZ_CP014263.1|WP_077131888.1|3431357_3432092_-|CRISPR-associated-endonuclease-Cas6
MPTTTQIPLTTITFPEIALRTRDAHKLRGYFGELFREHSPLLHNHLEADDADGNAGVKYRYAYPLVQYKVLNHVPTLVGAGEGAGLLAQLFLQMREINIARSEGDAASRPAETFPVLSKHIRHEQATLGMTDDLVDYRFETLWMALNQTNYRDYRHYTEAEQQAQLKRVLTSQILATFREFGLWLEPHERVMVRLRVQERQTQFKNQTMVAFSGGFTANVLLPNGLGLGKAVSRGFGVVMSDER
>NZ_CP014263.1|WP_077134011.1|3432100_3434392_-|CRISPR-associated-helicase/endonuclease-Cas3
MIDHLLAKTKDRESLSTHTDLVLGAWQELHTRYAAVLEEDESFWFDAFIAALFHDFGKASLNFQNMLRKELGESISENGYEPMRHEFLSGVLLAAHTMLKARSRQDIQPNPAQVFAVFTHHKDFTLDLFCKDADKQWKIRPSDADAFFAYASQRLGMYYSEKGAFLNDIETTWQFIEDKPASSLLMLKDHVVQSTLADLEEKRNYVYRKTYLLQKALLMIADWTASGHRKLETTLAYDVELIRQKIVERVAKAGGTFSGFREFQERSGQLSGNVLAIAPTGSGKTEAALLWATQREGYEKIVYLLPTRVTANALFKRLDSFFGYTADKKPERFTAVVHSSAKLFRLDLDENYENLNYLRESAFFKAVTVATVDQMLTQGFNLGWWEMKTFHLFRARVILDEIHAYAPYTLGLIVATIRYLRANFQTQFYVMTATMPQKLQVLLARELGIGDDKILRDQQLLDKKRNTFYTTEKTIDQLRPNVEADLREGKKVLIVVNTVDEAIRLYDQYASVKNRMCYHSRFIVKHRTEKERLILENEEKAPNQGFLLIATQVVEVSLDIDYQSLYTENAPIDAIIQRAGRINRKRSETLGKVVIFPHSETTEKHVYDEPQGILKKTFDELEKRKGTDLSEQDLLDLVEVVYDGWNVEADKQYIDALTKYERLLKKHCAYLYDFSGDLEQVFTREGLDTVNVIPNCYQIELANASILEKSKHEVAIRNHRFKSGRKEKDMKHSWFQYFDCDYSFEKGLRYKAKENHAGTTHHH
>NZ_CP014263.1|WP_077131889.1|3434396_3435110_-|CRISPR-associated-protein-Cas5
MLCCTIELKSVTASFRNPEFQNFHKSFPLPPPTALIGLAGAALGYSPRQAQDFFDTNGFRAGVSGKGEGMTRDLWKYDRLTGTGSSIILRELYVNTHYRLVFGSENHAAVEQLRQAFDRPFYALTLGQSDSLAKVMQTTLTDAVTDGRTLENTLVEGDIVPAILEQVLYGGTFALSLSTSDPIAYQLPTRFQYKSDYGMRTVAKRKLFSFVGPKVTFQNQTFPGVQVGDVFVPLFAL
>NZ_CP014263.1|WP_077131890.1|3435121_3436021_-|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR
MKTNSLTITYLSKVSFASLNGGDKEVDNIVTIKKVTLDNGDQLPYLSSQAVRRALRDKLEELGWAVSPVAKASEDKGAAKTSLDPAQYIDDDLFGFMDAAKGKDAEKGKATVRTSPVRVEALLALTKYQEDLDFGTNYMAKKVEGGQPNIFETEIHSGIYRGTILIELDRVGAGEGFEKTGKLSADERAKRVQGLIDAFQTMWSSGRQSRFLADISPKFMAAACMNSKNPIFLEAVRTDRNGQVDVAALQTVLSDYDQFITSSVLATQEGVFGKAEGVVSLKDGFSAIKQWIRDYYAAN
>NZ_CP014263.1|WP_077131891.1|3436010_3437792_-|hypothetical-protein
MSVEKITFNQTHNVFLDNGIVAMYRYLRRIEDGELGKLKKFSLTEGTHFGLEPDNLWLNHHDLFGLLEDLYYEMGREVYDTYTDKQLAEGGNLFFTVGQNGELTATPFPKMNTYGLTELLTNNAQGTTSKEVNTEKIESIRKRDSALADKIEVEFNNRKLKLLSKVYFNEPYTKLTRLEPPQNAYFEPGPNPCYLTGESVKRLVDAQNISPFISGISAFSSHRSTNDKKVSWKALYLSRFAAAACFYQYPGKLRDALNVYLIYSDNLKNLYELLRDKFDKITRPADLLRQQEYIANFPMSDENNALGRAGDFIGRNENLFYMLHTLYNSVMKDRKSFEQLEMLKMLGIADRSIGIVSLRAESFAATMRPNQFENLHHVKFVFALIHRFRQQGVSIPNVWQSLKIIKPSLQSNRDRYCMERQFREKFVGKVLNAQSILSDMEGFFNDCYGYLLDVLNEPGKSIGFKRYNDLVKFITQYELIVNQEVMQNEDLQKRALGLGAQVGQGILNYNQNDRKTNARQGRKYIIALRKANQFAGFMDQLSRVQSRFTLNISRDLLEGINEDNYAWIKQFVIISALNQINPELSPKSQTNEN
>NZ_CP014263.1|WP_077131892.1|3437995_3438208_+|hypothetical-protein
MTILQLPVPETTAERFRALSEQQQTFVSQLVTDCLSESSSLTQVMDYISFKAAQRGLTPEILQELLSSHP
>NZ_CP014263.1|WP_077131894.1|3438505_3440317_-|gamma-glutamyltransferase
MLKRILSGSLLLAVGLYACKTKPPVSTTPAVRESQGVYQYVEEIPTRTGTQASAFFSDKKGVVGRNGMVATAHPISSEVGLSILQAGGNAVDAAVAVHFALAVVYPFAGNLGGGGFMVYRDQAGKAYTLDYREKASGRATQNMYLDSAGNVRPSLSILGHLASGVPGTVDGMVEAHKRFGKLTWAQVLQPAVDLAANGFLLTDRDATGLNRIKGDLLKINPDKTYFLRSTTPGDTVTWHKGDRLVQTDLAKTLQRIQTRGRADFYEGETARLLAEEMRRGGGLITEDDLKNYHATWRDPIQATYKNYKIITMPPTSSGGVALVQLMRFTEPYPLRKWGWNADSTVQVMIEAERRVYADRSKFLGDPDFVKIPMAELMSPDYLRTRWTDFSFARATDSKAVRGGTIPGYESLETTHFSIVDKEGNAVSITTTLNGGYGSRVVVGGAGFFMNNEMDDFSVKPGVPNMFGLIGNQANAIAPNKRMLSSMTPTIVEKDGKLFMVVGTPGGSTIITSVYQTILNVIEHGMSMQQAVNALKFHHQWLPDKTIFENGAFSDNTVLKLQERGYILEKLTNTLGRMDCVMVRPDGSYEGASDPRADNTARGW

Crispr_ID: NZ_CP014263_5

• CRISPR_ID: NZ_CP014263_5
• CRISPR_location: 4399134-4399223
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP014263_5

Consensus_repeat	Method
CCGCGACCGCAATCGCGATGACCG	CRISPRCasFinder

spacers of NZ_CP014263_5

>5.1|4399158|42|NZ_CP014263|CRISPRCasFinder
GAACAATGACCGCTACGACGACCGTCGCAGTTCGTATGATGA

CRISPR arrays and Neighbor proteins around NZ_CP014263_5

CRISPR arrays

The CRISPR arrays of NZ_CP014263_5

>merge|NZ_CP014263|5|4399134-4399223|CRISPRCasFinder
CCGCGACCGCAATCGCGATGACCGGAACAATGACCGCTACGACGACCGTCGCAGTTCGTATGATGACCGCGACCGCAACCGCGATGACCG

>NZ_CP014263|5|6|4399134-4399223|CRISPRCasFinder
CCGCGACCGCAATCGCGATGACCG	GAACAATGACCGCTACGACGACCGTCGCAGTTCGTATGATGA
CCGCGACCGCAACCGCGATGACCG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014263.1|WP_077132635.1|4392902_4398386_+|alpha-2-macroglobulin-family-protein	unknown	unknown	gnl|CDD|225248
NZ_CP014263.1|WP_077132632.1|4383244_4384639_-|MBL-fold-metallo-hydrolase	unknown	unknown	gnl|CDD|224157
NZ_CP014263.1|WP_077132643.1|4409925_4410552_+|biopolymer-transporter-ExbD	unknown	unknown	gnl|CDD|376792
NZ_CP014263.1|WP_077132645.1|4411113_4411938_+|energy-transducer-TonB	unknown	unknown	gnl|CDD|367555
NZ_CP014263.1|WP_077132633.1|4388543_4392014_-|PKD-domain-containing-protein	unknown	unknown	gnl|CDD|369642
NZ_CP014263.1|WP_077134080.1|4384769_4387118_+|penicillin-binding-protein-1C	unknown	unknown	gnl|CDD|273954
NZ_CP014263.1|WP_077132638.1|4400967_4401819_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077132642.1|4409012_4409846_+|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl|CDD|376576
NZ_CP014263.1|WP_077132629.1|4380265_4381375_-|chorismate-synthase	unknown	unknown	gnl|CDD|235438
NZ_CP014263.1|WP_077132644.1|4410572_4411109_+|biopolymer-transporter-ExbD	unknown	unknown	gnl|CDD|376792
NZ_CP014263.1|WP_077132637.1|4400365_4400971_+|HupE/UreJ-family-protein	unknown	unknown	gnl|CDD|379373
NZ_CP014263.1|WP_077132640.1|4403476_4405882_+|M1-family-metallopeptidase	unknown	unknown	gnl|CDD|341067
NZ_CP014263.1|WP_077134082.1|4399856_4400369_+|gamma-carbonic-anhydrase-family-protein	unknown	unknown	gnl|CDD|100051
NZ_CP014263.1|WP_083732909.1|4387174_4388671_-|amidohydrolase-family-protein	unknown	unknown	gnl|CDD|238624
NZ_CP014263.1|WP_077132631.1|4382981_4383185_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077132628.1|4380016_4380223_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077132634.1|4392345_4392783_+|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl|CDD|379639
NZ_CP014263.1|WP_077132639.1|4401818_4403228_-|MBOAT-family-protein	unknown	unknown	gnl|CDD|224610
NZ_CP014263.1|WP_077132630.1|4381414_4382857_-|hypothetical-protein	unknown	unknown	gnl|CDD|379280
NZ_CP014263.1|WP_077132641.1|4405904_4408322_+|M1-family-metallopeptidase	unknown	unknown	gnl|CDD|341067

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP014263.1|WP_077132635.1|4392902_4398386_+|alpha-2-macroglobulin-family-protein	gnl|CDD|225248	COG2373, COG2373, Large extracellular alpha-helical protein [General function prediction only].	0
NZ_CP014263.1|WP_077132632.1|4383244_4384639_-|MBL-fold-metallo-hydrolase	gnl|CDD|224157	COG1236, YSH1, Predicted exonuclease of the beta-lactamase fold involved in RNA processing [Translation, ribosomal structure and biogenesis].	7.03211e-98
NZ_CP014263.1|WP_077132645.1|4411113_4411938_+|energy-transducer-TonB	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.	1.51621e-20
NZ_CP014263.1|WP_077132633.1|4388543_4392014_-|PKD-domain-containing-protein	gnl|CDD|369642	pfam07995, GSDH, Glucose / Sorbosone dehydrogenase. Members of this family are glucose/sorbosone dehydrogenases that possess a beta-propeller fold.	2.65807e-25
NZ_CP014263.1|WP_077134080.1|4384769_4387118_+|penicillin-binding-protein-1C	gnl|CDD|273954	TIGR02073, Includes:_Penicillin-insensitive_transglycosylase, penicillin-binding protein 1C. This subfamily of the penicillin binding proteins includes the member from E. coli designated penicillin-binding protein 1C. Members have both transglycosylase and transpeptidase domains and are involved in forming cross-links in the late stages of peptidoglycan biosynthesis. All members of this subfamily are presumed to have the same basic function. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan].	0
NZ_CP014263.1|WP_077132642.1|4409012_4409846_+|MotA/TolQ/ExbB-proton-channel-family-protein	gnl|CDD|376576	pfam01618, MotA_ExbB, MotA/TolQ/ExbB proton channel family. This family groups together integral membrane proteins that appear to be involved translocation of proteins across a membrane. These proteins are probably proton channels. MotA is an essential component of the flageller motor that uses a proton gradient to generate rotational motion in the flageller. ExbB is part of the TonB-dependent transduction complex. The TonB complex uses the proton gradient across the inner bacterial membrane to transport large molecules across the outer bacterial membrane.	1.45309e-33
NZ_CP014263.1|WP_077132629.1|4380265_4381375_-|chorismate-synthase	gnl|CDD|235438	PRK05382, PRK05382, chorismate synthase; Validated.	0
NZ_CP014263.1|WP_077132644.1|4410572_4411109_+|biopolymer-transporter-ExbD	gnl|CDD|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	4.579e-16
NZ_CP014263.1|WP_077132637.1|4400365_4400971_+|HupE/UreJ-family-protein	gnl|CDD|379373	pfam13795, HupE_UreJ_2, HupE / UreJ protein. These proteins contain many conserved histidines that may be involved in nickel binding.	4.17739e-55
NZ_CP014263.1|WP_077132640.1|4403476_4405882_+|M1-family-metallopeptidase	gnl|CDD|341067	cd09604, M1_APN_like, Peptidase M1 family similar to aminopeptidase N catalytic domain. This family contains bacterial M1 peptidases with smilarity to the catalytic domain of aminopeptidase N (APN; CD13; alanyl aminopeptidase; EC 3.4.11.2), a type II integral membrane protease belonging to the M1 gluzincin family. APN preferentially cleaves neutral amino acids from the N-terminus of oligopeptides and, in higher eukaryotes, is present in a variety of human tissues and cell types (leukocyte, fibroblast, endothelial and epithelial cells). APN expression is dysregulated in inflammatory diseases such as chronic pain, rheumatoid arthritis, multiple sclerosis, systemic sclerosis, systemic lupus erythematosus, polymyositis/dermatomyosytis and pulmonary sarcoidosis, and is enhanced in tumor cells such as melanoma, renal, prostate, pancreas, colon, gastric and thyroid cancers. It is predominantly expressed on stem cells and on cells of the granulocytic and monocytic lineages at distinct stages of differentiation, thus considered a marker of differentiation. Thus, APN inhibition may lead to the development of anti-cancer and anti-inflammatory drugs. APNs are also present in many pathogenic bacteria and represent potential drug targets. Some APNs have been used commercially, such as one from Lactococcus lactis used in the food industry. APN also serves as a receptor for coronaviruses, although the virus receptor interaction site seems to be distinct from the enzymatic site and aminopeptidase activity is not necessary for viral infection. APNs have also been extensively studied as putative Cry toxin receptors. Cry1 proteins are pore-forming toxins that bind to the midgut epithelial cell membrane of susceptible insect larvae, causing extensive damage. Several different toxins, including Cry1Aa, Cry1Ab, Cry1Ac, Cry1Ba, Cry1Ca and Cry1Fa, have been shown to bind to APNs; however, a direct role of APN in cytotoxicity has been yet to be firmly established.	3.79276e-142
NZ_CP014263.1|WP_077134082.1|4399856_4400369_+|gamma-carbonic-anhydrase-family-protein	gnl|CDD|100051	cd04645, LbH_gamma_CA_like, Gamma carbonic anhydrase-like: This family is composed of gamma carbonic anhydrase (CA), Ferripyochelin Binding Protein (FBP), E. coli paaY protein, and similar proteins. CAs are zinc-containing enzymes that catalyze the reversible hydration of carbon dioxide in a two-step mechanism, involving the nucleophilic attack of a zinc-bound hydroxide ion on carbon dioxide, followed by the regeneration of the active site by ionization of the zinc-bound water molecule and removal of a proton from the active site. They are ubiquitous enzymes involved in fundamental processes like photosynthesis, respiration, pH homeostasis and ion transport. There are three evolutionary distinct groups - alpha, beta and gamma carbonic anhydrases - which show no significant sequence identity or structural similarity. Gamma CAs are trimeric enzymes with left-handed parallel beta helix (LbH) structural domain.	3.24702e-75
NZ_CP014263.1|WP_083732909.1|4387174_4388671_-|amidohydrolase-family-protein	gnl|CDD|238624	cd01299, Met_dep_hydrolase_A, Metallo-dependent hydrolases, subgroup A is part of the superfamily of metallo-dependent hydrolases, a large group of proteins that show conservation in their 3-dimensional fold (TIM barrel) and in details of their active site. The vast majority of the members have a conserved metal binding site, involving four histidines and one aspartic acid residue. In the common reaction mechanism, the metal ion (or ions) deprotonate a water molecule for a nucleophilic attack on the substrate. The function of this subgroup is unknown.	5.64302e-75
NZ_CP014263.1|WP_077132641.1|4405904_4408322_+|M1-family-metallopeptidase	gnl|CDD|341067	cd09604, M1_APN_like, Peptidase M1 family similar to aminopeptidase N catalytic domain. This family contains bacterial M1 peptidases with smilarity to the catalytic domain of aminopeptidase N (APN; CD13; alanyl aminopeptidase; EC 3.4.11.2), a type II integral membrane protease belonging to the M1 gluzincin family. APN preferentially cleaves neutral amino acids from the N-terminus of oligopeptides and, in higher eukaryotes, is present in a variety of human tissues and cell types (leukocyte, fibroblast, endothelial and epithelial cells). APN expression is dysregulated in inflammatory diseases such as chronic pain, rheumatoid arthritis, multiple sclerosis, systemic sclerosis, systemic lupus erythematosus, polymyositis/dermatomyosytis and pulmonary sarcoidosis, and is enhanced in tumor cells such as melanoma, renal, prostate, pancreas, colon, gastric and thyroid cancers. It is predominantly expressed on stem cells and on cells of the granulocytic and monocytic lineages at distinct stages of differentiation, thus considered a marker of differentiation. Thus, APN inhibition may lead to the development of anti-cancer and anti-inflammatory drugs. APNs are also present in many pathogenic bacteria and represent potential drug targets. Some APNs have been used commercially, such as one from Lactococcus lactis used in the food industry. APN also serves as a receptor for coronaviruses, although the virus receptor interaction site seems to be distinct from the enzymatic site and aminopeptidase activity is not necessary for viral infection. APNs have also been extensively studied as putative Cry toxin receptors. Cry1 proteins are pore-forming toxins that bind to the midgut epithelial cell membrane of susceptible insect larvae, causing extensive damage. Several different toxins, including Cry1Aa, Cry1Ab, Cry1Ac, Cry1Ba, Cry1Ca and Cry1Fa, have been shown to bind to APNs; however, a direct role of APN in cytotoxicity has been yet to be firmly established.	1.01899e-137
NZ_CP014263.1|WP_077132634.1|4392345_4392783_+|nuclear-transport-factor-2-family-protein	gnl|CDD|379639	pfam14534, DUF4440, Domain of unknown function (DUF4440).	3.03344e-09
NZ_CP014263.1|WP_077132643.1|4409925_4410552_+|biopolymer-transporter-ExbD	gnl|CDD|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	1.97263e-14
NZ_CP014263.1|WP_077132639.1|4401818_4403228_-|MBOAT-family-protein	gnl|CDD|224610	COG1696, DltB, Predicted membrane protein involved in D-alanine export [Cell envelope biogenesis, outer membrane].	1.48463e-59
NZ_CP014263.1|WP_077132630.1|4381414_4382857_-|hypothetical-protein	gnl|CDD|379280	pfam13584, BatD, Oxygen tolerance. This family of proteins carries up to three membrane spanning regions and is involved in tolerance to oxygen in in Bacteroides spp.	1.73909e-41

Protein sequences

>NZ_CP014263.1|WP_077132635.1|4392902_4398386_+|alpha-2-macroglobulin-family-protein
MTRRRLLHSLLFIPLVFLLAHCSRLSFNEVNVVGRNFGDEVQQTQNLTFTFNKNVGPDEKNGALGEWDSTQYVRFKPAVRGKFRWTAPNELVFSPTVAFDPATDYRAELTADLLKRAPDKDLKVSGEEIDFHTPYLQLTGTETWWAKSRETGQPVAKAKLNFNYPVSAGEVSGKLTVATDEKPITVQLAPADGPTSVALTLLNAPAEKNEQPLTMKLGKGLTVPKTAYVSKEAIEETSTLPSRTSVEVVDVQTRFENNTGVVRVITTQELQAGKLSQYYTIQPEVETSAELTENGFVIRGNFNETDTYVLTLTDQIRGTLGTKLSESITRDLFFGKMPASIQFANKKALYLSSKGARNVGLSIVNVPKVQVRIAKLYENNLLNYFRSNRYEQYSEGQDGIWAPNGTFNYNDDESGDLSDVLVNKTVETIDLPKVRGVSALNVSLPDQDNNFRGVYLVSVGSKDEAYLSATQLVSVSDIGLVARQTNDEVLVWANSIRTAEPLQNVELTLVSSNNQSVYTLKTDGSGFARFEKVGEKAPGFKIALITARTDGPTQNADFNFLFLPDTQVETSRFAVEGKRDNTSGFDAFVYGDRDIYRPGETIHFNTVIRSQSWQSVGEVPVLIRLLAPNGREVRAFRKTTNSQGAISTDVPLDPAAVTGTYTIEVLNANNIQLTTESVSVEEFIPDRIKVDVLTDRTTYKAGQTITLSTTATNLFGPPAADRSYEMELQLKRKTFAPKDFAEYNFAMSEMGASAVAFPKEVRQGRTNANGQATERFVIPATYQDIGILEGKLFVSVFDENGRPVNRLRRFDVQTQDVFFGVRLPDYYVTTNAPVAAEVVAVDASGTLRPSATATVEVVRYDYQTVIEKKENDQIKYTTKQREKVVYTNTLTFKGGKASFRYVPTVSGEYEIRIRRAGESATGYATTGFYAYGWGSTSASSFEVSQEGQVLMTLDKETYETGDRARILFKAPFDGKLLVTIERNRVLEHKWLTTSNKSAEFSFSVGSDHLPNVYVTATLIRAMDATNLPLTVAHGFAPVPVQDKDSKLAVAITAATQSRSKTKQTIRVKTARNAQVTVAVVDEGILQLKNFKTPDPHGFFYQKRALEVNSHDLYALLYPELSLQSQSSVGGDGYDLERRVNPLSNGRVRLVALWSGILDTGLDGEAEFTVDVPQFSGDLRVMAVAYKDNAFGSANSNMKVADPIVISAGVPRFLSPGDQLDLPVNLSNTTKKAATVTARLSLTGPLAIDSLSSQQLNIPAGREARATFRLSAKQAIGPGGITFTVNGLGETFTEKIDVTVRPAASLQKTTLSGAVAGGKTQTLNVTGGFLPGTARASMTLSRSPVAQYGRELSFLLGYPHGCIEQTISRAFPQLYFADLTKQIGASNTYFVRNGDSDLNPATNVRQAIQTVEGLQTARGGFSMWPGMVGLAVDPWASAYALHFLTEAQEAGYEVRGSVLSSAIDYLTTYTNNPATESVAQFDEAGGRTVRNVASRTSIYALYALATAGKPNRPIMNYYKQNAQTLTTDSRYLLAAAFFRLGDTRSYTALLPKRYTDNTTARETGGSYASPLRNLALTLDALVETDRSNLQIPTLARQLSGALRQNTYLNTQEAAFAFLALGKLARQNAGTTTTATLSAGGKSLGSMTDAFLNVKRLLTNQPLLLSAKGSGNVYYFVQSEGVPQAGQIAEEDNGLRVRRQYLDRNGQPISEVRQNDLVVVKVTVASTNGLNIDNVVVTDLLPAGLEVENPRLTEQRDMDWLKGAATPDHFDLRDDRINFYTSATGAEKVFYYQARAVSKGRFVLGPVSADAMYNGEYRSYHGAGVVVVR
>NZ_CP014263.1|WP_077132634.1|4392345_4392783_+|nuclear-transport-factor-2-family-protein
MKSILLLVAGLVFATATFAQTAPTDPMQDPTALTNAFFKAMLDEDGTLNKYLTSDFSITSFDGQTVDGDLLAQGVGGGFVIVETATISDARTRQYNNDAAVTTGNWKAKGSIQGQGFDSNVAFSVTSVKQGTGWKIANIQFTAAK
>NZ_CP014263.1|WP_077132633.1|4388543_4392014_-|PKD-domain-containing-protein
MRLACFFSVCRLTISLLVFISSIRSGFAQLPSGFSKTTIQDNYTSPVGIVFSTDGNRFFVWEKSGRVWVSVWNGSAYVRQATPVVDIREEVGEWNDFGLHSICLDPNFESNGLMYLFYTVDLHHVLNFGTAQYSSTTNQYHNATISRVSRFRVQNTNGTLTANSRTVLVGESATTGIPVTFESHAGGTILFGEDGTLLVSTGDGAHHEGVDVGGRTDTYFQASLNFGMMRSNENVGALRAQMVRSLCGKVLRIDPATGNGVSSNPFYDAANPRSPQSRVWTLGLRNPYRMSLKPNTGSTNPADGNPGTLLIGDVSWYQIEEFHVVDKAGLNCGWPVYEGLDPTISYNGTNVRNLDEPGTPTFESLCVQPTTFADNPNPTLRRFTHSRPALDYSHGTARTRVPAFSGTTPIARLVGSTGAPAGTPFFGKCVIGGVYYTGTQFPAMYRNTYFFTDFSQHWIKNLDLHDEGDHVVHEVRNFAPDNFDPSILDIKMNPRDGSLFYVRIQGTVSRISYGGNQPPVANASSTINYGTSPLSVTFTGSNSVDPEGLPLTYLWDFGDGTTSTSANPVHVFTGTGVRKFTVTLTVRDNANQASLPKQLVVSVNNTPPTVQITNPAQGTLYTMSQATPYTLQANVTDTDQTGMGYEWQVSLEHNNHSHPEPVITTASPTVTISPVGCSPNETYYYLITLTVTDNGGLKATHSVTLYPDCNSASSLVSNVVATPQLNSVRVSWINPTATFNEILVAARPTGGFTDIPIGTSYTADPSYTGNGSPIEGGKVVYKGIGNEVTVTNLNPLVQYYFRVYTRVGGIWNGGVEVSAIPNLPPVAPAIQPPAAATGQSYAYTIPVFTDPENQALVYNLTGLPAWLSYNTTSRQLTGTPTQSASHTLTISATDPGGLITAVPFVIVAGPNQPPTAPTLPVLTAEVNQFFTYTTPAFTDPEGKSLTYSVTNLPGWLSFNSGTRQFSGTPTVASSYSITVRATDPSGLFTSRVLVINTSVNQPPIPPTIGPQTAEIGYFFTYTVPAFTDPEGQTLTYSASGLPGWLSFDAVNRRLTGTPTQAGSFTVTVRATDPRSLTASVQVVISTGVCSMVTVKNGSWDDPTVWSCNRVPASTDAVRVEHVISLPNNYTALARRVTFAGGKTLSVGDGARLQFSP
>NZ_CP014263.1|WP_083732909.1|4387174_4388671_-|amidohydrolase-family-protein
MLYGSSMSSVCLTTTRHWPEELRSQVGKRCLWAMEHGYSLAHNILRVDAPLSKHKLSMRLLIPFLLLLVSSPVLAQPKTKLFIRVGKLYDAKNSSFLTNQQIIVADGVIEAVGHNIVKPANATVLNLTTCTVTPGLIDMHTHLLLHQKQTKDGLEVASKVPASERIKSGLVFARQHIEAGITTVRDLGNSGQYLDSQLQKTLAESKEIGPTMYVSGPIISPPGGQFSKLFPADSFVINQEYRVVSGVEDARAAVLEHKKRGVNVIKVCMNTENRVLAPEEIAAIVQTAHKNGLSVTAHATYDDSAKDAVLAGVDGIEHGYILSDSTLALMAQRGTYLVPTDVSREKGELLVAGIGMVGKEAEDYLKSALDGFHDRLRRAVNKGVMIVSGSDFYNDVKGIERGEGAVDVIQSYYEAGLPAKDVLRYATYNAAKALGLSERLGVISKGAKADLVFFNGDLENDFAQSLANVKMVLKEGRIIYPKAKPQSKTKLKNPQGSK
>NZ_CP014263.1|WP_077134080.1|4384769_4387118_+|penicillin-binding-protein-1C
MLSKKMSNWRELVKRLWRKRLTKAVLTTFSLFLLLDLLFPLNTRVPYSTLIISRDGQILHAFLSRDDKWRMYAELPEITPTLRNAILFKEDKYFYYHPGFNPVAMLRAAGRNLLTGRRTSGASTITMQTVRLLEPRKRTYLSKAIELFRAIQLEWHYSKDEILQLYLNLIPYGGNIEGLKSASLLYFGKPPQLLSLAELTTLTIIPNRPSSLRLGHSNARIVQERNRWLTRFRTAGLYNDATIADALTEPLTAYRREAPQQAPHLARRLRTDHPDTPIVRASVRADAQATAERIVQNYANRLRGLAIHNAAVLIVDNATREIVAYVGSADFRNAFDGGQVDGVRAVRSPGSALKPLLYGLAFDAGIITPKTKLADVPTNFSGYEPDNYDRRFNGPVTAEFALANSLNIPAVALLNELGTSSFVSALGKAGFVSVKKQAKDLGLSLVLGGCGVTLEEMTRLYVGLANGGQVKPIHLTASSATKEVPASGAEETVLSPEATYLVTQTLVQITRPDLPNNFDNSYHLPRIAWKTGTSYGRRDAWSIGYNRRYTVGVWVGNFSGVGVAELSGANTATPLLFQLFNALDYNSPSGWFRPPTNLSHRLICPETGDVPGDSCHHPVTDAFIMGVSRYRPCQHRKAIWTNAAGTISYCAHCRPADAVRRLYPNLAPNVLAFYQTQRIPFRTVPPHNPACERVYGDAGPLITSLNDRSEYYINPRQPAELELGCQAGSDVKTVFWYLNDKFYRRATPTEAVFFKPRPGPLKISCADDRGRHSDLHVLVKAE
>NZ_CP014263.1|WP_077132632.1|4383244_4384639_-|MBL-fold-metallo-hydrolase
MTIQFFGAARTVTGSKHLVTTDSGTQILLDCGLFQGINTDELNQTFGFNPARVDYMVLSHAHIDHAGLIPRLVKQGFRGPIYTTLATIDLCDVMLRDSARIQERDLERVNERRTRRGQPELEALYDEQDVEQALSQMRPVNYNQPFVITEDVTGLLTDAAHLLGSASISLTIRENGAEKRLFFSGDIGRPDDKILRRPDSFPQADYIICESTYGDRLHEPEPDMKSHLLRIVHKTCIENRGKLIIPAFAVDRTQELIYALDQLSSEGRLPKLPVYIDSPMAVKATQVMHMHQDNFNPDILVYINKDGDAFSFPNLHYVSDVNESKAINNRQGPCIIIAPSGMAEAGRIKHHIKNNIDDPQTTILLVGYASPNSLGGALKRGDKEVTIFGDRYEVKARVEIMDSFSAHGDYREMLDFLSCQNPVLVKRVFLVHGEYEKQLVWKDKLETAGFQHVAIPEMGEKVVL
>NZ_CP014263.1|WP_077132631.1|4382981_4383185_+|hypothetical-protein
MLSMLEYIKTILQKVSFDKALFEKELAKAIKMLIPEEVTQLKRWCYAQFGKMYRVVLNRCFARVRYS
>NZ_CP014263.1|WP_077132630.1|4381414_4382857_-|hypothetical-protein
MFLAVFRKYFALFFCLPIVTFGQVIDNAATIEFSATNFPIERPFVITVSIPNSETRPTISFPDITGFSKKGTSASVTTVEIGGKTVVNQIITQNYQARTPGRFRLPPFSITTNGTTVRSEGAELTVRPTATLPGSASALLENTLPKNPAFLTLRATKSSIYVGESIGLTLSFFVADNYPYVLNFTALDKQLQTIIKKIRPANAWEENLNINELKAVPVQVGGKPFREYKLYQAVFFPLSTRPLRLPAVTLQLTRSRPLIGPPAPTPETVSFTSRPLNVAVRALPAHPLRGRVPVGVFRLEESLDRRRIVVSRSVRYAFSVVGEGNIAALPAPAMLNPNPDVDVFPPEERLTLSRTVAGVTGSKTFTYFLVPHQQSPIPLAGRFQWIYFNPQLARYDTLRPALVLQVGTTNGNTSPAKMGNSPETGRDTVSAPAGSMSIYDGIETLDSSRQPISISVLVRAAANVFIVLMLLGMIFVFFKR
>NZ_CP014263.1|WP_077132629.1|4380265_4381375_-|chorismate-synthase
MSSTYGTLFKISTFGESHGPAIGVVIDGCPAGLTFDTEFIQHELDRRKPGQSRITTQRREADEFDVLSGVFDGQTQGTPIALIIRNTDQRSKDYGHIAQQFRPSHADYTYQAKYGSRDYRGGGRSSARETAARVAAGAVAKLLLAQHGVQIRAYVSQVGALKLDKPYTELNLNLTEENPVRCPDSDMAGQMFQYIDETRKRGDSIGGVIDCVITGVPAGWGEPVFDKLHAELGKAMLSINAVKGFEYGSGFAGVELYGSQHNDEFYTDETGKVRTRTNHSGGIQGGISNGEAIYFRTAFKPVATIMQDQDSVDVDGQPVTVSGKGRHDPCVVPRAVPIVEAMAALVLVDMMLRNEAAQVGRTTKQAEFL
>NZ_CP014263.1|WP_077132628.1|4380016_4380223_+|hypothetical-protein
MITIRNKYLLAAAGFWLLGLIFVLIGAAGRSNQWDSAGTLLTIGILAQAIGFGLLGFVLMQAVFSKKK
>NZ_CP014263.1|WP_077134082.1|4399856_4400369_+|gamma-carbonic-anhydrase-family-protein
MALIKPVRGIAPQFGENCWFAENATIVGEVTFGRDCTVWFNAVVRGDVNSITIGDRTNIQDGAVIHCTYQRYKTTIGSFVSIAHNAVVHGCTLADNVLIGMGAIVMDGAVVGAGSIIAAGAIVTQNTIVPPGSIYAGNPARFLKAVSPEQAEIFARTANNYVMYADWFKE
>NZ_CP014263.1|WP_077132637.1|4400365_4400971_+|HupE/UreJ-family-protein
MNDFLIYLRLGFDHITDPSGYDHILFVVALCTVYTLRQWRQVLILVTAFTVGHSITLALATLQLVRYDTAVIELLIPITILITAITNFFFKEQKSRSLSKPKPFNQAWRYGLALVFGLIHGLGFSNYLRSLLGREASILQPLLAFNIGLELGQLLIVGLVLGIAYVTIEVLRRSRLRWTLIVSGIVAGMALSLIINNELLN
>NZ_CP014263.1|WP_077132638.1|4400967_4401819_-|hypothetical-protein
MIRKAILTTVLLLLLYSTFIHVCQSHIRRTGLTTQQTNTIKAEEFAYETDHQADTIIVGSSMSNRLLFDGMQSSYCNLSMEGMASIDGLGLIAHMRQHPRLLLVEMNSLDRLPDTTLALHLTEPGWALVREYVPLTRLKYQPLGVAKALFRDWYSPPAQAMGAESIDTAFASKLIAERLHDMMRIPSEGELREKIAKVAEHIRHFQKAGTQVVFFEMPTDPRVRNAALSCRIRHVIEETFPPAAYRYIRYPVTVYQTTDGVHLPQTEGIRYSRYLYQQLCQKL
>NZ_CP014263.1|WP_077132639.1|4401818_4403228_-|MBOAT-family-protein
MLFTSFSFVVLVAVTFCFYYLPPLHRWQVPILIAASLVFYMVNQADLLWLLLLSISVNIVASYLVVYGRTDLRLFHATWGVVVNLGILCFFKYGPLLSQTFLPANSTLGETLSALPLPVGISFFTFQGISLVVDTYRNRDVPRFRSLIARNLAQHAQTVFFFKAFFPQLISGPIVKAHFFLPQISRKYWADIQWENCFRTLVVGYFLKMVVADNLKDHTMLITYPYFEGYSSLTLLGLLFGYSMQIFADFAGYSLIALGLAGLFGYTFPANFNFPYVAVSFADFWRRWHISLSSFLREYLYIPLGGNRHGVWRTYLNLMLTMVLGGLWHGAAWSYAVWGFGHGLALALERFVDQHIPLKSTRITQVIRSSVVFSYVTLLWLLFKLPDFNHVVAYCRAIVNNVGKPHDSRVLSLILLYSLGVVGYHVHYLMRSSESHYEPSTWEFVGCGILLFFIITNSGSAGTFIYFQF
>NZ_CP014263.1|WP_077132640.1|4403476_4405882_+|M1-family-metallopeptidase
MQKIILLIVALTTLAQTASAQSGQVPTQNANSRFEQLGSLLPTPNTFRTASGAPGKDYFQNRADYDIKVELDDQKQRIIASETITYLNNSTDALRYIWLQLDQNLFRPDADGNTARTNSINAERGASPAQLDPGANLRGKNYGHSITSIRDAAGKSLPYRINQTMMRIDLPTPVQPGKSVTFSIDWNFTIVDADATNARSGYEYFPKDGNYVYEMAQWFPRLCAYNDVTGWQNKQFLGQGEFTLIFGNYKVAITAPNDHVVGATGELQNPAQVLTATQIARWNSAKGRGNKPGENPIAIVTQAEAEAAEKGKPTGKKTWIYKASNVRDFAFASSRKFIWDALQPTVEGKPVWAMSLYPKEANPLWGQYSTRLVAHTLRSYSRRTFAYPYPVAYSVHGPVGGMEYPMMSFNGARPEPDGTYSVNTKNFLIQVVIHEVGHNFFPMIVNSDERQWSWMDEGLNSFLEGLACLEWDPNFPARGIEPQYIVPYMQLDAASQVPIMSSSDNILPNTFGPNAYSKPATALNILRETVMGRDLFDYAFKEYARRWAFKSPEPADFFRTLEDASGVDLDWFWKGWFYGTEAVDQELLDVDWFQPSSQNPEVAKAEARTAAQRRLNTISRQRDAATKDQTVVAQDSTMTDFYNRYDPYAVTEADKKRYQDYLATLSEEERKTLASSSQTHYYTLSVKNKGGLPMPVIIRMQFEDGTDSVARFPAEIWRFNDVSVKKVIATSKKVTQWTLDPYREIADIHPENNNFPVIAEPTRFQLFKQRGNAGTQTPNPMQQQRQNQPANRPAVQGSGRN
>NZ_CP014263.1|WP_077132641.1|4405904_4408322_+|M1-family-metallopeptidase
MKNRLLIACAVFLTGTAALAQPGQAPTQNANSRFEQLGSVLPTPNTFRTASGAPGKDYFQNRADYDIKVELDDAQQKIIGSETVTYYNNSTDVLPYIWLQLDQNLFAKGSTGSVTRTGGVNENGMSFSQLQNLTSVRERSQQQASDKYGYTITAVTDGKTRSPLKYTINQTMMRIDLPAPLRPGGSYSFNIDWNYFVTEYYGRSGMEFFPTDGNYNYFIAHWFPRLCAYNDVTGWQNKQFLGQGEFTLIFGNYKAAITVPADFVVGATGECQNYKQVLNATQQKRLAQAANSKTPVVIVTQDEAVAAEKTKAGGTTAKKTWVYKADNVRDFAFTASRRFIWDAMQTDVYGDGRKIWSMSFYSKEGNPLWGQYSTRVVEHTLKSYGNRTIKYPYPVAISCHATPGGGMEYPMISFNGGRPEPDGTYSEQVKYGMIGVIIHEVGHNFFPMIVNSDERQWTWMDEGLNTFCQYLAEKEWDYNYPTRRGEPQQIVDYMKSDKAVLSPIMTSSDNVISLGPNAYAKPATALNILRETVMGRDLFDYAFKEYARRWAFKSPEPADFFRTLEDASGVDLDWFWKGWFYGTEAVDQELLDVDWFQPSSQNPEVAKAEARTAAQRRLNTISRQRDAATKDQTVIAQDSTMTDFYNRYDPYAVTEADKKRYQDYLATLSEEERKTLASSSQTHYYTLSVKNKGGLPMPVIIRMQFEDGTDSVARFPAEIWRFNDVSVKKVIATSKKVTQWTLDPYQEIADIDTENNAFPRVSQPTRFQLFKQRSNPFAPQGPNPMQQQRQATGATPPARQGSGRN
>NZ_CP014263.1|WP_077132642.1|4409012_4409846_+|MotA/TolQ/ExbB-proton-channel-family-protein
MKTQTPSPAPAKAAAPKKKSGGLNPALVIPILLLIGILVYMFVFGDGSHFQEGDNTKEPLPGDYFGTVYKGGFIVPILFTCFLTVLVFSIERFITIGRANGTGSIDDFVRKIKSLLDRNEVAAAIAECDKQKGSIGNVVKTALLKYQQLATDTQLDKEQKLAALQKEVEEATTLELPMLEKNLTIIATLASVSTLIALLGTVLGMIRAFAAMGATGQPDTAALSTGISEALVNTALGIGTAAIATIMYSYFTTRIDVLTYNIDEIGLSIQQNFAAHY
>NZ_CP014263.1|WP_077132643.1|4409925_4410552_+|biopolymer-transporter-ExbD
MPAVKVKRASSAVDMTAMCDVAFLLLTFFILTAQFRAQDAATIETPSSISGIKVPDKDIMTIGLDRDGKVYFGIDNQQYRMAMLDNIATAKGISFSDKEKKEFALMSNFGMPINQLKSFLSLSHEQMGKIKQPGIPTDSTGAAASNELKDWVFNARKANNNLRIALKGDNLAKFPAFKNVLATLQAQNINKFNLITGTEAPPAGWKAD
>NZ_CP014263.1|WP_077132644.1|4410572_4411109_+|biopolymer-transporter-ExbD
MAEINTGGGGGKHDGGKVRSKKASTRVDMTPMVDLGFLLITFFILATTLSKPSSMTLNVPDKTKEVETEPIKASNVMTVFLGKDNKAHYIFGKAATEDPEVKTVGYGYEFRQAILENTRKVGSDKFVVVIKPTKESSYRNMVDVLDEMAITKTKRYALVDLLTPDEKTLLKDKVKLDT
>NZ_CP014263.1|WP_077132645.1|4411113_4411938_+|energy-transducer-TonB
MAENPNTATLDDIVFANRNKAYGAYDLRKGYSRTVTRALIIGGVVFTLGVLAPTIITALTPEPEEQAMVEVDLMKLPPPPIDPNEPPPPPPPPVELPKVNTVKFLPPEVKPDEEVPEETPPPAVEELKEAVAAEKTQEGDPNAEEVIAAPEASAAPTKVEVAVEAAPKEEEIFTVVEQQPEFPGGMAALGQFLGKNLRYPAAAQRANVSGRVFVSFVVNTDGSIQDVQVLKGLGFGTDEEAQRVVKSMPKWRPGKQSGRPVRVKYNLPINFTLE

Crispr_ID: NZ_CP014263_6

• CRISPR_ID: NZ_CP014263_6
• CRISPR_location: 5278563-5278661
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP014263_6

Consensus_repeat	Method
TGTTCGGGATGTAAATCCCGAAC	CRISPRCasFinder

spacers of NZ_CP014263_6

>6.1|5278586|53|NZ_CP014263|CRISPRCasFinder
CTGATAACTGCGGGTATTCACCCGCGCAAGCGGACAAACGTCCGCTGTTAATA

CRISPR arrays and Neighbor proteins around NZ_CP014263_6

CRISPR arrays

The CRISPR arrays of NZ_CP014263_6

>merge|NZ_CP014263|6|5278563-5278661|CRISPRCasFinder
TGTTCGGGATGTAAATCCCGAACCTGATAACTGCGGGTATTCACCCGCGCAAGCGGACAAACGTCCGCTGTTAATAGGTTCGGGATGTAAATCCCGAAC

>NZ_CP014263|6|7|5278563-5278661|CRISPRCasFinder
TGTTCGGGATGTAAATCCCGAAC	CTGATAACTGCGGGTATTCACCCGCGCAAGCGGACAAACGTCCGCTGTTAATA
GGTTCGGGATGTAAATCCCGAAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014263.1|WP_077133305.1|5275008_5275986_+|radical-SAM-protein	unknown	unknown	gnl|CDD|223609
NZ_CP014263.1|WP_077133309.1|5280185_5280644_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077133311.1|5282709_5283696_-|N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase	unknown	unknown	gnl|CDD|271335
NZ_CP014263.1|WP_157579291.1|5288757_5289720_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077134155.1|5278719_5280066_-|xylose-isomerase	unknown	unknown	gnl|CDD|235487
NZ_CP014263.1|WP_077133306.1|5275995_5277093_-|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl|CDD|275036
NZ_CP014263.1|WP_077133303.1|5272637_5273948_+|DUF5103-domain-containing-protein	unknown	unknown	gnl|CDD|379920
NZ_CP014263.1|WP_077133312.1|5283710_5284277_-|pentapeptide-repeat-containing-protein	unknown	unknown	gnl|CDD|224276
NZ_CP014263.1|WP_077133300.1|5266753_5267635_-|cysteine-synthase-CysM	unknown	unknown	gnl|CDD|236972
NZ_CP014263.1|WP_077133307.1|5277201_5278020_+|hypothetical-protein	unknown	unknown	gnl|CDD|235664
NZ_CP014263.1|WP_077133304.1|5274059_5274902_+|acetyl-CoA-carboxylase-carboxyltransferase-subunit-beta	unknown	unknown	gnl|CDD|235547
NZ_CP014263.1|WP_077133318.1|5290582_5291305_-|copper-homeostasis-protein-CutC	unknown	unknown	gnl|CDD|225684
NZ_CP014263.1|WP_077133315.1|5288303_5288765_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP014263.1|WP_077133317.1|5289723_5290581_+|formyltetrahydrofolate-deformylase	unknown	unknown	gnl|CDD|235676
NZ_CP014263.1|WP_077133299.1|5265640_5266696_-|quinone-dependent-dihydroorotate-dehydrogenase	unknown	unknown	gnl|CDD|235388
NZ_CP014263.1|WP_077133308.1|5278082_5278517_-|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl|CDD|378987
NZ_CP014263.1|WP_077133301.1|5267867_5268293_+|LytTR-family-transcriptional-regulator	unknown	unknown	gnl|CDD|197918
NZ_CP014263.1|WP_077133310.1|5280760_5282581_-|glycogen-synthase	unknown	unknown	gnl|CDD|340824
NZ_CP014263.1|WP_077133313.1|5284381_5287210_+|restriction-endonuclease-subunit-M	unknown	unknown	gnl|CDD|223363
NZ_CP014263.1|WP_077133302.1|5268358_5270059_-|AMP-binding-protein	unknown	unknown	gnl|CDD|235923

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP014263.1|WP_077133305.1|5275008_5275986_+|radical-SAM-protein	gnl|CDD|223609	COG0535, COG0535, Predicted Fe-S oxidoreductases [General function prediction only].	3.0147e-25
NZ_CP014263.1|WP_077133311.1|5282709_5283696_-|N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase	gnl|CDD|271335	cd04513, Glycosylasparaginase, Glycosylasparaginase and similar proteins. Glycosylasparaginase catalyzes the hydrolysis of the glycosylamide bond of asparagine-linked glycoproteins. This enzyme is an amidase located inside lysosomes. Mutation of this gene in humans causes a genetic disorder known as aspartylglycosaminuria (AGU). The glycosylasparaginase precursor undergoes autoproteolysis through an N-O or N-S acyl rearrangement of the peptide bond, which leads to the cleavage of a peptide bond between an Asp and a Thr. This proteolysis step generates an exposed N-terminal catalytic threonine and activates the enzyme.	5.41808e-135
NZ_CP014263.1|WP_077133317.1|5289723_5290581_+|formyltetrahydrofolate-deformylase	gnl|CDD|235676	PRK06027, purU, formyltetrahydrofolate deformylase; Reviewed.	8.05035e-147
NZ_CP014263.1|WP_077134155.1|5278719_5280066_-|xylose-isomerase	gnl|CDD|235487	PRK05474, PRK05474, xylose isomerase; Provisional.	0
NZ_CP014263.1|WP_077133306.1|5275995_5277093_-|T9SS-type-A-sorting-domain-containing-protein	gnl|CDD|275036	TIGR04183, hypothetical_protein, Por secretion system C-terminal sorting domain. Species that include Porphyromonas gingivalis, Fibrobacter succinogenes, Flavobacterium johnsoniae, Cytophaga hutchinsonii, Gramella forsetii, Prevotella intermedia, and Salinibacter ruber average twenty or more copies of a C-terminal domain, represented by this model, associated with sorting to the outer membrane and covalent modification.	6.56737e-08
NZ_CP014263.1|WP_077133303.1|5272637_5273948_+|DUF5103-domain-containing-protein	gnl|CDD|379920	pfam17116, DUF5103, Domain of unknown function (DUF5103). This is a family of Bacteroidetes proteins of unknown function.	7.78521e-114
NZ_CP014263.1|WP_077133312.1|5283710_5284277_-|pentapeptide-repeat-containing-protein	gnl|CDD|224276	COG1357, COG1357, Pentapeptide repeats containing protein [Function unknown].	3.15868e-14
NZ_CP014263.1|WP_077133300.1|5266753_5267635_-|cysteine-synthase-CysM	gnl|CDD|236972	PRK11761, cysM, cysteine synthase CysM.	0
NZ_CP014263.1|WP_077133307.1|5277201_5278020_+|hypothetical-protein	gnl|CDD|235664	PRK05995, PRK05995, enoyl-CoA hydratase; Provisional.	3.72251e-63
NZ_CP014263.1|WP_077133304.1|5274059_5274902_+|acetyl-CoA-carboxylase-carboxyltransferase-subunit-beta	gnl|CDD|235547	PRK05654, PRK05654, acetyl-CoA carboxylase carboxyltransferase subunit beta.	3.05195e-150
NZ_CP014263.1|WP_077133318.1|5290582_5291305_-|copper-homeostasis-protein-CutC	gnl|CDD|225684	COG3142, CutC, Uncharacterized protein involved in copper resistance [Inorganic ion transport and metabolism].	4.31444e-91
NZ_CP014263.1|WP_077133299.1|5265640_5266696_-|quinone-dependent-dihydroorotate-dehydrogenase	gnl|CDD|235388	PRK05286, PRK05286, quinone-dependent dihydroorotate dehydrogenase.	0
NZ_CP014263.1|WP_077133308.1|5278082_5278517_-|nuclear-transport-factor-2-family-protein	gnl|CDD|378987	pfam12893, Lumazine_bd_2, Putative lumazine-binding. This is a family of uncharacterized proteins. However, the family belongs to the NTF2-like superfamily of various enzymes, and some of the members of the family are putative dehydrogenases.	0.000223107
NZ_CP014263.1|WP_077133301.1|5267867_5268293_+|LytTR-family-transcriptional-regulator	gnl|CDD|197918	smart00850, LytTR, LytTr DNA-binding domain. This domain is found in a variety of bacterial transcriptional regulators. The domain binds to a specific DNA sequence pattern.	3.51476e-17
NZ_CP014263.1|WP_077133310.1|5280760_5282581_-|glycogen-synthase	gnl|CDD|340824	cd03793, GT3_GSY2-like, glycogen synthase GSY2 and similar proteins. Glycogen synthase, which is most closely related to the GT3 family of glycosyltransferases, catalyzes the transfer of a glucose molecule from UDP-glucose to a terminal branch of a glycogen molecule, a rate-limit step of glycogen biosynthesis. GSY2, the member of this family in S. cerevisiae, has been shown to possess glycogen synthase activity.	0
NZ_CP014263.1|WP_077133313.1|5284381_5287210_+|restriction-endonuclease-subunit-M	gnl|CDD|223363	COG0286, HsdM, Type I restriction-modification system methyltransferase subunit [Defense mechanisms].	1.83128e-26
NZ_CP014263.1|WP_077133302.1|5268358_5270059_-|AMP-binding-protein	gnl|CDD|235923	PRK07059, PRK07059, Long-chain-fatty-acid--CoA ligase; Validated.	0

Protein sequences

>NZ_CP014263.1|WP_077133308.1|5278082_5278517_-|nuclear-transport-factor-2-family-protein
MKFLCLLLLTAPAFAQNPDEAAVRKTISSLFEGMKRADSTTLKPLFLPNARLQTVLNKAGDVSVKDDPIAGFVASVGKAKAGALDERLGDYMVHIDGDLATAFTPYQFYYNGEQHHCGANAFTLVRVGEVWKIQTIIDTRRKCQ
>NZ_CP014263.1|WP_077133307.1|5277201_5278020_+|hypothetical-protein
MLYTAQQTAQLPPNGFRYLRTSLNNNVLTITLNRPEKKNALHPPMLAELAFALAYAHHTATVWLVVLAAAGDTFCAGMDLRALAEGETEASTVPEPAGPVRLGELMAGLHKPCLARVQGPVYAGGFLLVGGSTYVLAAENATFSLPEVKRGLFPFQVLAVLIDIMPVRQALDLCLRARTLSAAQAQDIGLATHLVPADELDDAVYNLANELKQFSPTALHYGLRAAHTLKSLPSNEQQAYLYEQFQQLQQTPDAKEGMAAFLEKRRPEWGKS
>NZ_CP014263.1|WP_077133306.1|5275995_5277093_-|T9SS-type-A-sorting-domain-containing-protein
MKTLTLLSLLLLVRIAEATHLIGGYIQTKPISGLQYEITVTLYMYEIGGQVASGADDNVSICFGDGVTQSVARVARVITDDRQYSSNVYRVVHTYPGPATYRVTTFVPNRTPARNNGGPNQPFGLSTTFLAGMGQTPALSFPWVSLVLKTNQLAIVPLKATDAEGDSLAYRLAWPLVSLANVPCQPGDADGYQYPNAVARRGAFTINSRTGDLVWDAPTQEGRYNVAIMVLEYRRGALISQTIQEISVVVVDQPGTPGTIPPYEPAQTIGLITTTEAWRDNGPLLQAYPSPADGTLQVELLSPVPALVHLTLTDANGRVLQTAEPTRATRAYEKALNTSYLQSGMYILRADVDGQILTRKVLVEH
>NZ_CP014263.1|WP_077133305.1|5275008_5275986_+|radical-SAM-protein
MRLVRSPVLCNYYVTYRCNATCGFCDIWERPSPYVTLDNARANLRDLRRLGVRVIDFTGGEPLLHRQLPELLEEAKRLGFITTVTTNALLYPKQAERLRGLVDMLHFSLDSPVAEEHDRSRGVRCFDKVMESIQIARQLGERPDILFTVFEHNVQQIRDMYDTICRPNKLVLILNPVFEYNGVDTGGALSTDALQQLTNWGRQPGVYLNDAFVQLRRDGGNHVDKPVCRAGSTTIVISPENKLVLPCYHLGLKDFSINDDLYTLYRSEEVQKMVALEGRLPACEGCAINCYMQPSFAVDVNRYFWKALPSTLKYNWMKGTWKQLF
>NZ_CP014263.1|WP_077133304.1|5274059_5274902_+|acetyl-CoA-carboxylase-carboxyltransferase-subunit-beta
MSWFVRKDKGIQTPTEMKREAPDGLWYQCPNCKKAMHTREHKLNAYTCVHCNYHEKIGSEAYFSILFDNNTFTELDANMMSADPLNFTDTKSYPGRVKATMMKTGLKDAVRTAYGPMNDQIVTVACMDFSFIGGSMGSVVGEKIARAIDHAIASRTPFLMISRSGGARMMEAGYSLMQMAKTSAKLALLSQARLPYVSLLTDPTTGGVTASYAMLGDFNIAEPGALIGFAGPRVIRETIGKDLPKGFQEAEFVLEHGFLDFIVDRKDLKDKLSSLFGMLE
>NZ_CP014263.1|WP_077133303.1|5272637_5273948_+|DUF5103-domain-containing-protein
MTKPLAFAFFILHLSLPHAFAQSVPNIDRIYDPQVQTVLLYPLISQKPADRDAGSPTLLLNPPVVSLDEPVPLQLEFDDLTADYRSFRAKLVHCDANWQKSVLNDIEYTFEYNDNPITDYAVSVNAKVPYYHYRFTLPRVKLPGNYLLVVYDERNPRNTILTRRFSTYQNRLTVAAAVRFSTDPARQFTDQQIDLNIDYKGYQVLSPQDDFRVVIRQNYRDDRILTNLRPTNVRAFDQVLEYRVVDLSNTIPGGNEFRFFDIRTVVSRGNFIERINRPADRNIAYVQADVPRSQGAYIQSDDFNGQYIIDNRETGNGATGADYIETVFTLRTPEIPGVSLFVNGAFNLWQLNDRNRMTFDAGEGTYRAAILLKQGVYNYNYVVQTSGSQPRIDEMYIEGSYSATENEYEVFVYHRPPAARADQLVGYRRIGVNRRK
>NZ_CP014263.1|WP_077133302.1|5268358_5270059_-|AMP-binding-protein
METQQTNLTYPWRRFYPKGVPHEINPDAYPSLAALMEEGFQRFADRPAYACMGKHITFSELDKLSQQFASFLQNDLKLQKGDRIAIQMPNTLQYPVAMFGALRAGLAVVNTNPLYTPREMQHQFKDSGAKAIVILANFAGNLEKILDRTDIKHVVITELGDLLGFPKKLLVNAVVKYVKKLVPAYKLPNAISFGDALNRGIRQPFRPVDIKNTDMAFVQYTGGTTGVSKGAVLSHRNIISNVECQHVWMSPGNVSDGEGVIVAALPLYHVYALTTNALAALKSGAMNLLITNPRDLNAFIDDLKKYKVTAFTGVNTLYNGLLNHPRITEVDWSYLSVTSAGGMALQTTVAERWAKLTGNTPCEGYGLTETSPVLCSNPVDGSVRVGTIGIPWPSTDMKIIREDGTDAAIGEPGEIVARGPQVFGGYYNRPDETEKCMIDGWFKTGDVGVMNEDGFFKIVDRKKDMILVSGFNVYPNEIEDVVAQCPGVLEAACIGVPDAKSNEAVKVFVVKKDPELTVDTIKAFCRENLTAYKVPRYIEFRTELPKSNVGKILRKPLRDEELAKIK
>NZ_CP014263.1|WP_077133301.1|5267867_5268293_+|LytTR-family-transcriptional-regulator
MKAAVLTKPLTNAHVKQIAGQFDMSDLTLPFWGYRKKMPMHRIVRLEGEGNYTVFHFDDGTQLMVSLTLKKMQSRLPSNVFVRPHKKNIINLLYLEGIHPDRQQLSVSLVNGDRVEVSRRKASNFIRQVKGFQQELQAIEA
>NZ_CP014263.1|WP_077133300.1|5266753_5267635_-|cysteine-synthase-CysM
MATLLDLVGNTPLVEINRMGANRINPNVKIYGKLEGNNPGGSVKDRAASSMIEGALLRGDLKPGMKLIEATSGNTGIALAMIARLYSIDIELVMPANSTRERVLTMEAFGAKVILSETIEAARDYAEAQVQQGGYLMLNQFANPDNYLAHYRTTGPEIWRDTAGQITHFVSSMGTTGTIMGTSRFLKEQNSTVQIVGCQPTDGSSIPGIRKWPTEYLPKIYDAQRVDRIIEVSEADAVETTRQLANVEGIFAGMSSGGSVWSALKLAEELESGVIVCIICDRGDRYLSSGLFG
>NZ_CP014263.1|WP_077133299.1|5265640_5266696_-|quinone-dependent-dihydroorotate-dehydrogenase
MYKRILLPILFRFDAETIHHTVTSLLKFALAIPGVSAICRKLYVLEDKRLERTVFGLTFPNPVGMAAGFDKNAELVSELSDLGFGFVEIGTVTPRPQPGNPRPRLFRLKADAGLINRMGFNNKGVGPAVERLRNVGRNRVGQPDGGRRVIVGGNIGKNKDTPNEQALSDYLASFRELFDVVDYFVVNVSSPNTPGLRDLQEREPLTNLLTALQAENRLYAAPKPILLKIAPDLTNGQLDDIIAIVSETGIAGVIATNTTVSRANLLTDAAIVEQMGAGGVSGQPLRERATEVIRYLHTKSGGAFPIIGVGGIASAADAQEKLQAGASLVQVYTSFIYEGPGLAKKICQGIL
>NZ_CP014263.1|WP_077134155.1|5278719_5280066_-|xylose-isomerase
MSQTSLTLGDKAYFPFVEKPIQYEGRESDNPLAFKFYDASRPILGTPMRDLFRFAVAYWHTFCGTGNDPFGPGVKHFPWDVNAQTDPLGAAFSKADAAFEFITKMGMEYYCFHDVDVSPEGKSNSEFESNFRKVVDYLKQKQTASGVKLLWGTANLFSHERYMNGASTNPDFHVLAHGGWQVKNAIDATIELGGRGYTFWGGREGYMSLLNTNMKREQEHLAKFLQISRDYARRQGFTGAFYIEPKPMEPTKHQYDFDAATVVGFLHRNGLQDDFELNVETNHATLANHTFAHELQVAADNNMLGSIDANRGDYQNGWDTDQFPVDVYELTEAMLVILEAGGFRSGGVNFDAKTRRNSTDLEDIFIAHIGGMDTFARAAIATEAILSQSKYKQLRADRYASYDSGAGADFEAGKLTLEDLRQYALDNGEPKQISGKQELYEMIVNQYI
>NZ_CP014263.1|WP_077133309.1|5280185_5280644_-|hypothetical-protein
MNPIFTKLNYKDQSEVAVVNAPDAFLPALETMRPLATIVTDPALIQTGGFILAFVKTQQEVDTLTEALAAKVEGDGLLWFAYPKGTSKRHQCEFNRDTGWAELGKQGFEGVRQVAIDEDWSALRFRRAEYIKKMTRQASRAMSEHGKKRVAP
>NZ_CP014263.1|WP_077133310.1|5280760_5282581_-|glycogen-synthase
MESVFSTSKRKLLLEIAWEVCNQVGGIYTVIRSKVPAMVEKWDDNYVAVGPYFPQRATAEFEPITDSDETEIGQTVRKMRQMGFGVEYGYWLVTGRPRVVLFDINSVSVDQLNYIKTQLWLNHQLTTLNVEDLVNQTIVFGEMVRQFITLLAADHARRVDLVAHFHEWMASTGLPDLRRDNIKVATVFTTHATMLGRYLAQNEPGFYGKLPFFDWLKEARHYGIETQATVERLAALQSHVFTTVSDVTARECEVFLGRNPDLVLPNGLNITRFAAVHEFQNLHVRFKQKIHEFVMGHFFQSYSFDLEKTLYFFTSGRFEFSNKGYDLTLEALARLNYRMREANMDMTVVMFMVTKQPYTSINPDVLHSRALLDEIQETTQAIEKQVGERLFQATASDPNGTTLPDLNSFVDEYWRLRLRRTVQSWKTKRLPPFVTHNLVQEDDMTRFIRQANLVNNEYDRVKVVYHPDFIASTNPLFGLDYSQFVRGCHLGVFPSYYEPWGYTPLECVVRGIPTVTSDQSGFGDFIMQIMRDYENRGIYVINRRTQNFNEAADQLTNVLFRFVKMAQRDRIQQRNRVESIAEVFDWTNLRSYYDTAHDLALKRKKP
>NZ_CP014263.1|WP_077133311.1|5282709_5283696_-|N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase
MLNRRRFLTLSSLSALSPKLFALTPPTGPPDRPIVVSTWNQPKANAAAEAVLNRSGRALDAVEAGVRVPEADPNDTSVGYGGLPDRDGRVTLDACIMDERGNAGSVTFLENIMHPISVARAVMEKTPHVMLSGEGAQAFALSQGFKKENLLTKESEAKWREWLKTAEYKPKVNIERHDTIGMLAIDAKGDASGACTTSGLAYKMHGRVGDSPIIGAGLFVDNEIGGACATGLGELVLRTCGSFLAVELMRQGKTPQQACEEVIRRIAKGSFAKDGKYLNGAGTIDDVQVGVLAVSKQGEIGAYSLQPGFNYTVSQGGQTRVVEAKSWK
>NZ_CP014263.1|WP_077133312.1|5283710_5284277_-|pentapeptide-repeat-containing-protein
MDYLDLLFDRPDQLPTRWADHTFEQCTFRKLNLSGQSLAGANFIDCRFDHCDLTRAGLKNTKLYDIQFLHCNLQHVDFSVCNPFGFHVNFQECPLNYAVFIDRKLKKARFADCSLREAHFIKSDLSGTTFHHCNLEFATFDNNDLTQADFSSSYNLTLNPDSNKLKKARFSLHNLPGLLMKHELVIVH
>NZ_CP014263.1|WP_077133313.1|5284381_5287210_+|restriction-endonuclease-subunit-M
MIQSAIQQLISRLGFTSDVSGNLFVKTFAQHKNYKLEVDLVNRRIVYAEPVKVHDKTTSHFDAPENFVVLECVNRLLEKGYEPQHIELERRWSLGRTGKSGKADVTVMGRDGQSLIVIECKTAGSEYEKEKRNTTASGGQLFSYLQQDRNTRFLCLYASELRNAAVHYENAIVQIKDRPEVTELVRTDPDTVAYETAKTKEELHRAWKENFNCYFAPNGIFDEEAQAYNPEFKPIKRKDLRPFTPEEGRQLFNAFEEILRHNNISDRSNAFNRILSLILCKIVDERKQPNEETGFQVKEATDTPESIQERLQRLYQQGMQDYLKEEFTYISEEQVDEIVSRFPRQTAQREIREIVRKLKFYSNNEFAFKEVHNESLFNENAKVLNEILALLQYKQFRYQRTDAHQYKHQKRYLGDFFELLLDAGYKQTAGQFFTPLPVARFIVKSLPLREMMQEKLAAQRPNFLPYVIDYACGSGHFLTEVMEEIQHHIDQLPPTYSDDVNQNLTHWQKADWTGEFIYGIEKDYRLARTAKVACFMNGDGEANIIFGDGLEDYTRPVKGRNYKFAPQFDAVVANPPYSIQSFKTHLGLKNSQFSLYDSLTESASEIEVLFVERTAQLLREGGVAGVVLPSSILSNTGIYTRARELMLQRFELRAIVEFGSNTFMATGTNTVTLFLTRRNDRLADDFRAVADDFILKNQFRPDDFTDTEALLAAYASRHNLSVADYRSLLSKTPTEVLLQSDLWRDYDRWFADLTETKNRRDTKKAEGKAFAKLSPDEQQQELTRLFYERVLPREHDRFLYFCLTYQQPTLIVRLPADGAEEKRFLGYEFSRRRGDEGIKLYQDAQGRHQTTLYDEEELHHPDKLNTLVWQALSGRQPTIPDALRPHANVVDLADCLDVTRVEFEKQIGLATQTTNSALYWTFVKQGIPLTTLNDIKNAAKTW
>NZ_CP014263.1|WP_077133315.1|5288303_5288765_+|hypothetical-protein
MKQIYPPLLAAGFQEIGPWQLDQQFLEPFGENERRLHLINRLRVYLNDLINLGIPLEIWLDGSFVTRKPEPDDVDMVVWVQASDIDQLPAAHKLKFRLLLMDRDRVRSLYDVDVYWAIPTSDHEREKWQCMFGFDQSPVPKPKGIFKLTLNHA
>NZ_CP014263.1|WP_157579291.1|5288757_5289720_+|hypothetical-protein
MPNIAHIDSMLRMARQTLAERERERETQPDSFAWQCAVESAQMHVDELTRQLVDAKKQREIELVEIRLTGKLARFGSLPMSVLGRISTAFEEVLVQAGRTLRQQETVEAIRSLFDVRLKAVAPGSTRLFITLQTNPDLFGDSLAETCLTHTFNLLKVETPVEAQTQVRKVGRKGTQQLSKLLKVLDENYLEAHVNWQSPTDKFFTWEGKLGRIRELSQTFDRIVANEPEEVAVEGTVYTESIRKRFEVQDASGFIYGGSVPDSLMNSLTALRVGEPCRAILLETIHENPTTGQQQKLYQLKYIAPLPAQSTLQPTQLSLF
>NZ_CP014263.1|WP_077133317.1|5289723_5290581_+|formyltetrahydrofolate-deformylase
MTPPDKHILLMDGPDSKGLIYHVTGVLYRHGLNIIHNDEYVSPNGQFFMRTEFESAPDVTFDSAALLSELNTALPNAEGITFRLNPKRKKNIVVLVTKEHHCLGDLLIRYAFDELDADILAVVSNYNHLQPLVSKFGIPFHYVSHEGRSREEHEEAILRTLSIYEPEYLVLAKYMRVLTSDFVNRFPNRIVNIHHSFLPAFVGASPYRQAYERGVKIIGATAHFVNNDLDEGPIIAQNVKEVDHRHTASDMATEGRDVEKIVLSQALKLVFNDRVFIAGNRAIVL
>NZ_CP014263.1|WP_077133318.1|5290582_5291305_-|copper-homeostasis-protein-CutC
MVEVCAYSLESCLTAQRAGAGRIELCGGMAEGGTTPSAGLIQLARQYLTIPLYVMIRPRGGDFLYSDTEFMVMQADIELARSFGADGVVLGILNATGTVDEIRTRQLVELAHPLPVTFHRAFDMTRDPLEALEAVIRTGAARILTSGQQPTAEAGLPILRQLVKQAAGRIEIMGGAGVNAQNATRLREAGVDALHLSGSQRNESGMLFRQAAVSMASAVPGEYERIEADEEKIRAVCSLC

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	346443-346462	0	1.0
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	643158-643177	0	1.0
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	2625296-2625315	0	1.0
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	3793393-3793412	0	1.0
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	4890628-4890647	0	1.0
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	5442389-5442408	0	1.0
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	1221377-1221396	1	0.95
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	2870139-2870158	1	0.95
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	2908267-2908286	1	0.95
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	2908310-2908329	1	0.95
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	2908353-2908372	1	0.95
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	5565105-5565124	1	0.95
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	247596-247615	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	397799-397818	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	627044-627063	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	1002678-1002697	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	1166926-1166945	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	1171555-1171574	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	1434167-1434186	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	1474729-1474748	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	2785588-2785607	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	2951606-2951625	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	4036397-4036416	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	5168321-5168340	2	0.9
NZ_CP014263_3	3.1|2174182|20|NZ_CP014263|CRISPRCasFinder	2174182-2174201	20	NZ_CP014263.1	5234502-5234521	2	0.9

1. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 346443-346462, mismatch: 0, identity: 1.0

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaattgtagaga	Protospacer
********************

2. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 643158-643177, mismatch: 0, identity: 1.0

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaattgtagaga	Protospacer
********************

3. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 2625296-2625315, mismatch: 0, identity: 1.0

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaattgtagaga	Protospacer
********************

4. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 3793393-3793412, mismatch: 0, identity: 1.0

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaattgtagaga	Protospacer
********************

5. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 4890628-4890647, mismatch: 0, identity: 1.0

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaattgtagaga	Protospacer
********************

6. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 5442389-5442408, mismatch: 0, identity: 1.0

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaattgtagaga	Protospacer
********************

7. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 1221377-1221396, mismatch: 1, identity: 0.95

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcacttgtagaga	Protospacer
********** *********

8. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 2870139-2870158, mismatch: 1, identity: 0.95

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcgattgtagaga	Protospacer
*********.**********

9. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 2908267-2908286, mismatch: 1, identity: 0.95

cggatggtcaattgtagaga	CRISPR spacer
cggatagtcaattgtagaga	Protospacer
*****.**************

10. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 2908310-2908329, mismatch: 1, identity: 0.95

cggatggtcaattgtagaga	CRISPR spacer
cggatagtcaattgtagaga	Protospacer
*****.**************

11. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 2908353-2908372, mismatch: 1, identity: 0.95

cggatggtcaattgtagaga	CRISPR spacer
cggatagtcaattgtagaga	Protospacer
*****.**************

12. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 5565105-5565124, mismatch: 1, identity: 0.95

cggatggtcaattgtagaga	CRISPR spacer
cggacggtcaattgtagaga	Protospacer
****.***************

13. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 247596-247615, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcacctgtagaga	Protospacer
********** .********

14. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 397799-397818, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggttaactgtagaga	Protospacer
********.**.********

15. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 627044-627063, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cgggtggtcaactgtagaga	Protospacer
***.*******.********

16. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 1002678-1002697, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtctactgtagaga	Protospacer
********* *.********

17. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 1166926-1166945, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcacctgtagaga	Protospacer
********** .********

18. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 1171555-1171574, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcacctgtagaga	Protospacer
********** .********

19. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 1434167-1434186, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcattcgtagaga	Protospacer
********** *.*******

20. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 1474729-1474748, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaaccgtagaga	Protospacer
***********..*******

21. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 2785588-2785607, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaaccgtagaga	Protospacer
***********..*******

22. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 2951606-2951625, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggacggtcaactgtagaga	Protospacer
****.******.********

23. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 4036397-4036416, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcaaccgtagaga	Protospacer
***********..*******

24. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 5168321-5168340, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcacctgtagaga	Protospacer
********** .********

25. spacer 3.1|2174182|20|NZ_CP014263|CRISPRCasFinder matches to position: 5234502-5234521, mismatch: 2, identity: 0.9

cggatggtcaattgtagaga	CRISPR spacer
cggatggtcacctgtagaga	Protospacer
********** .********

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP014263_4	4.7|3425428|37|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR	3425428-3425464	37	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1921781-1921817	7	0.811
NZ_CP014263_4	4.4|3425206|38|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR	3425206-3425243	38	NZ_CP032696	Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525b, complete sequence	166546-166583	9	0.763
NZ_CP014263_4	4.8|3425502|36|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR	3425502-3425537	36	NZ_CP049157	Caballeronia sp. SBC1 plasmid pSBC1_1, complete sequence	1307680-1307715	10	0.722
NZ_CP014263_4	4.8|3425502|36|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR	3425502-3425537	36	NZ_CP049317	Caballeronia sp. SBC2 plasmid pSBC2-1, complete sequence	336728-336763	10	0.722

1. spacer 4.7|3425428|37|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.811

-cctgctggcagtggtggccggtggcttaatcctttac	CRISPR spacer
gctttgcggca-tggtggccggtggcctgatcctttac	Protospacer
 *.*  .**** **************.*.*********

2. spacer 4.4|3425206|38|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP032696 (Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525b, complete sequence) position: , mismatch: 9, identity: 0.763

gcgcatgtcggcctccgggtttgccagcaactggtaca	CRISPR spacer
gcgcatgtcggcctcggcgtttgccagcatgtcggcgg	Protospacer
*************** * ***********  * *   .

3. spacer 4.8|3425502|36|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049157 (Caballeronia sp. SBC1 plasmid pSBC1_1, complete sequence) position: , mismatch: 10, identity: 0.722

ctggagcaataccgagagtttaccatcgggctatat	CRISPR spacer
gccaagcaataccgtgagttttccatcgggcacggt	Protospacer
 . .********** ****** *********   .*

4. spacer 4.8|3425502|36|NZ_CP014263|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049317 (Caballeronia sp. SBC2 plasmid pSBC2-1, complete sequence) position: , mismatch: 10, identity: 0.722

ctggagcaataccgagagtttaccatcgggctatat	CRISPR spacer
gccaagcaataccgtgagttttccatcgggcacggt	Protospacer
 . .********** ****** *********   .*