CRISPRimmunity

Please click to download your results

Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Target MGE spacer number	Prophage number
NZ_CP015201	Chryseobacterium glaciei strain IHBB 10212 plasmid pMP02, complete sequence	0 crisprs	NA	0	0
NZ_CP015199	Chryseobacterium glaciei strain IHBB 10212 chromosome, complete genome	2 crisprs	DEDDh,WYL,cas3,csa3,RT,PD-DExK	1	4
NZ_CP015200	Chryseobacterium glaciei strain IHBB 10212 plasmid pMP01, complete sequence	0 crisprs	NA	0	0

Results visualization

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP015199_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP015199_1

842914-843072

Orphan

Consensus_repeat	Method
CTGAATAGAAGAAGCTTCGTTTCTTCT	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP015199_1

>merge|NZ_CP015199|1|842914-843072|CRISPRCasFinder
CTGTACTCCTGTAGCTTCATTTCTTCTGCCTAACTGTACCTGAACATCAGTATTGTCATCTCCAAGCTGAATAGAAGAAGCTTCGTTTCTTCTGCCGTTCTGAAGCTGATAAGCAAAGTTATCACTACCCAACTGAATAGAAGAAGCTTCATTTCTTCT

>NZ_CP015199|1|1|842914-843072|CRISPRCasFinder
CTGTACTCCTGTAGCTTCATTTCTTCT	GCCTAACTGTACCTGAACATCAGTATTGTCATCTCCAAG
CTGAATAGAAGAAGCTTCGTTTCTTCT	GCCGTTCTGAAGCTGATAAGCAAAGTTATCACTACCCAA
CTGAATAGAAGAAGCTTCATTTCTTCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP015199.1\|WP_066751325.1\|845631_846969_+\|peptidoglycan-synthetase	unknown	unknown	gnl\|CDD\|223844
NZ_CP015199.1\|WP_066751340.1\|852744_853032_+\|antibiotic-biosynthesis-monooxygenase	unknown	unknown	gnl\|CDD\|224278
NZ_CP015199.1\|WP_066751305.1\|833265_833937_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP015199.1\|WP_066751309.1\|837951_839463_-\|carboxypeptidase-like-regulatory-domain-containing-protein	unknown	unknown	gnl\|CDD\|372685
NZ_CP015199.1\|WP_066751322.1\|845188_845626_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_066759482.1\|836412_836889_+\|OsmC-family-protein	unknown	unknown	gnl\|CDD\|224678
NZ_CP015199.1\|WP_066751313.1\|840871_841282_-\|curli-assembly-protein-CsgF	unknown	unknown	gnl\|CDD\|371165
NZ_CP015199.1\|WP_066751331.1\|848213_849809_+\|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|275036
NZ_CP015199.1\|WP_066751338.1\|852130_852745_+\|NAD(P)H-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|376808
NZ_CP015199.1\|WP_027388329.1\|834076_834367_+\|integration-host-factor-subunit-beta	unknown	unknown	gnl\|CDD\|259858
NZ_CP015199.1\|WP_066751333.1\|849961_850903_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP015199.1\|WP_066759484.1\|841293_842022_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|337812
NZ_CP015199.1\|WP_066751328.1\|847098_847974_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381359
NZ_CP015199.1\|WP_066751307.1\|834742_836302_+\|ribonuclease-E/G	unknown	unknown	gnl\|CDD\|378414
NZ_CP015199.1\|WP_066751311.1\|839474_840839_-\|curli-production-assembly-protein-CsgG	unknown	unknown	gnl\|CDD\|367655
NZ_CP015199.1\|WP_066751315.1\|842032_842431_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_066751336.1\|851040_851781_-\|metallophosphoesterase-family-protein	unknown	unknown	gnl\|CDD\|365906
NZ_CP015199.1\|WP_054511251.1\|844369_845176_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP015199.1\|WP_066759483.1\|837109_837757_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225107
NZ_CP015199.1\|WP_066751319.1\|843712_844342_+\|CoA-pyrophosphatase	unknown	unknown	gnl\|CDD\|239518

Protein	Function_ID	Function_description	E-value
NZ_CP015199.1\|WP_066751325.1\|845631_846969_+\|peptidoglycan-synthetase	gnl\|CDD\|223844	COG0773, MurC, UDP-N-acetylmuramate-alanine ligase [Cell envelope biogenesis, outer membrane].	5.22112e-71
NZ_CP015199.1\|WP_066751340.1\|852744_853032_+\|antibiotic-biosynthesis-monooxygenase	gnl\|CDD\|224278	COG1359, COG1359, Uncharacterized conserved protein [Function unknown].	2.05546e-20
NZ_CP015199.1\|WP_066751305.1\|833265_833937_+\|response-regulator-transcription-factor	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	9.22637e-22
NZ_CP015199.1\|WP_066751309.1\|837951_839463_-\|carboxypeptidase-like-regulatory-domain-containing-protein	gnl\|CDD\|372685	pfam13715, CarbopepD_reg_2, CarboxypepD_reg-like domain. This domain family is found in bacteria, archaea and eukaryotes, and is approximately 90 amino acids in length. The family is found in association with pfam07715 and pfam00593.	6.21437e-10
NZ_CP015199.1\|WP_066759482.1\|836412_836889_+\|OsmC-family-protein	gnl\|CDD\|224678	COG1764, osmC, Organic hydroperoxide reductase [Secondary metabolites biosynthesis, transport and catabolism].	2.07197e-29
NZ_CP015199.1\|WP_066751313.1\|840871_841282_-\|curli-assembly-protein-CsgF	gnl\|CDD\|371165	pfam10614, CsgF, Type VIII secretion system (T8SS), CsgF protein. The extracellular nucleation-precipitation (ENP) pathway or Type VIII secretion system (T8SS) in Gram-negative (diderm) bacteria is responsible for the secretion and assembly of prepilins for fimbiae biogenesis, the prototypical curli. Besides the T2SS that can be involved in the assembly of prototypical Type 4 pilus, the T4SS that can be involved in the biogenesis of the prototypical pilus T, the T3SS involved in the assembly of the injectisome and the T7SS involved in the formation of the prototypical Type 1 pilus, the T8SS differs in that fibre-growth occurs extracellularly. The curli, also called thin aggregative fimbriae (Tafi), are the only fimbriae dependent on the T8SS. Tafi were first identified in Salmonella spp and the controlling operon termed agf; however subsequent isolation of the homologous operon in E coli led to its being called csg. In the absence of extracellular polysaccharides Tafi appear curled, although when expressed with such polysaccharides their morphology appears as a tangled amorphous matrix. CsgF is one of three putative curli assembly factors appearing to act as a nucleator protein. Unlike eukaryotic amyloid formation, curli biogenesis is a productive pathway requiring a specific assembly machinery.	5.00999e-44
NZ_CP015199.1\|WP_066751331.1\|848213_849809_+\|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.	7.21912e-13
NZ_CP015199.1\|WP_066751338.1\|852130_852745_+\|NAD(P)H-dependent-oxidoreductase	gnl\|CDD\|376808	pfam02525, Flavodoxin_2, Flavodoxin-like fold. This family consists of a domain with a flavodoxin-like fold. The family includes bacterial and eukaryotic NAD(P)H dehydrogenase (quinone) EC:1.6.99.2. These enzymes catalyze the NAD(P)H-dependent two-electron reductions of quinones and protect cells against damage by free radicals and reactive oxygen species. This enzyme uses a FAD co-factor. The equation for this reaction is:- NAD(P)H + acceptor <=> NAD(P)(+) + reduced acceptor. This enzyme is also involved in the bioactivation of prodrugs used in chemotherapy. The family also includes acyl carrier protein phosphodiesterase EC:3.1.4.14. This enzyme converts holo-ACP to apo-ACP by hydrolytic cleavage of the phosphopantetheine residue from ACP. This family is related to pfam03358 and pfam00258.	3.11698e-30
NZ_CP015199.1\|WP_027388329.1\|834076_834367_+\|integration-host-factor-subunit-beta	gnl\|CDD\|259858	cd13836, IHF_B, Beta subunit of integration host factor (IHFB). This subfamily consists of the beta subunit of integration host factor (IHF) and IHF-like domains. IHF is a nucleoid-associated protein (NAP) that binds and sharply bends many DNA targets in a sequence specific manner. It is a heterodimeric protein composed of two highly homologous subunits IHFA (IHF-alpha) and IHFB (IHF-beta). It is known to act as a transcription factor at many gene regulatory regions in E. coli. IHF is an essential cofactor in phage lambda site-specific recombination, having an architectural role during assembly of specialized nucleoprotein structures (snups). IHF is also involved in formation as well as maintenance of bacterial biofilms since it is found in complex with extracellular DNA (eDNA) within the extracellular polymeric substances (EPS) matrix of many biofilms.	4.92824e-32
NZ_CP015199.1\|WP_066751333.1\|849961_850903_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	8.64026e-35
NZ_CP015199.1\|WP_066759484.1\|841293_842022_-\|hypothetical-protein	gnl\|CDD\|337812	pfam10627, CsgE, Curli assembly protein CsgE. Curli are a class highly aggregated surface fibers that are part of a complex extracellular matrix. They promote biofilm formation in addition to other activities. CsgE is a non-structural protein involved in curli biogenesis. CsgE forms an outer membrane complex with the curli assembly proteins CsgG and CsgF.	9.76272e-10
NZ_CP015199.1\|WP_066751328.1\|847098_847974_-\|aldo/keto-reductase	gnl\|CDD\|381359	cd19133, AKR_AKR5F1, the AKR5F family of aldo-keto reductase (AKR). Klebsiella sp. 2,5-diketo-D-gluconic acid reductase (2,5-DKG reductase) is a founding member of aldo-keto reductase family 5 member F1 (AKR5F1). It catalyzes the reduction of 2,5-diketo-D-gluconic acid (25DKG) to 2-keto-L-gulonic acid (2KLG).	3.82078e-148
NZ_CP015199.1\|WP_066751307.1\|834742_836302_+\|ribonuclease-E/G	gnl\|CDD\|378414	pfam10150, RNase_E_G, Ribonuclease E/G family. Ribonuclease E and Ribonuclease G are related enzymes that cleave a wide variety of RNAs.	2.82363e-123
NZ_CP015199.1\|WP_066751311.1\|839474_840839_-\|curli-production-assembly-protein-CsgG	gnl\|CDD\|367655	pfam03783, CsgG, Curli production assembly/transport component CsgG. CsgG is an outer membrane-located lipoprotein that is highly resistant to protease digestion. During curli assembly, an adhesive surface fibre, CsgG is required to maintain the stability of CsgA and CsgB.	2.07199e-75
NZ_CP015199.1\|WP_066759483.1\|837109_837757_+\|response-regulator-transcription-factor	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	4.08325e-33
NZ_CP015199.1\|WP_066751336.1\|851040_851781_-\|metallophosphoesterase-family-protein	gnl\|CDD\|365906	pfam00149, Metallophos, Calcineurin-like phosphoesterase. This family includes a diverse range of phosphoesterases, including protein phosphoserine phosphatases, nucleotidases, sphingomyelin phosphodiesterases and 2'-3' cAMP phosphodiesterases as well as nucleases such as bacterial SbcD or yeast MRE11. The most conserved regions in this superfamily centre around the metal chelating residues.	1.02519e-11
NZ_CP015199.1\|WP_054511251.1\|844369_845176_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	2.16121e-19
NZ_CP015199.1\|WP_066751319.1\|843712_844342_+\|CoA-pyrophosphatase	gnl\|CDD\|239518	cd03426, CoAse, Coenzyme A pyrophosphatase (CoAse), a member of the Nudix hydrolase superfamily, functions to catalyze the elimination of oxidized inactive CoA, which can inhibit CoA-utilizing enzymes. The need of CoAses mainly arises under conditions of oxidative stress. CoAse has a conserved Nudix fold and requires a single divalent cation for catalysis. In addition to a signature Nudix motif G[X5]E[X7]REUXEEXGU, where U is Ile, Leu, or Val, CoAse contains an additional motif upstream called the NuCoA motif (LLTXT(SA)X3RX3GX3FPGG) which is postulated to be involved in CoA recognition. CoA plays a central role in lipid metabolism. It is involved in the initial steps of fatty acid sythesis in the cytosol, in the oxidation of fatty acids and the citric acid cycle in the mitochondria, and in the oxidation of long-chain fatty acids in peroxisomes. CoA has the important role of activating fatty acids for further modification into key biological signalling molecules.	2.48453e-48

>NZ_CP015199.1|WP_066751315.1|842032_842431_-|hypothetical-protein
MFKLGWSVFALLIFLSVKSQLLDWDRINSNTVLNVIAGQNPDQMMSYSNIIQMGDANNAELSLNAKTNISIKQLGDYNSLYFNNSFTDTETKTAITTQGNNNIIDVTGSNSISDGLQIQVKGDNKTIFMRNY
>NZ_CP015199.1|WP_066759484.1|841293_842022_-|hypothetical-protein
MKNFYSLILCSFIFLSVSISGQEDKKINAKIESKTMEGQINLKAVVTNSTAIYKELNYLLVSIKKGNGGNLSNNQQSGKFSINPNETKVLSEINVNLEKKDALKVFLYVKDEETQKLIAKDSLELNNDSFKKKVSKVEEDVVFELKGLTIDETKSKVGKDFYDFFYLQYSQLPDKSNSAITISELPGRGTNGQINIEIDDKVVYSFMTNPSEDYLKEQLTNSLKYIKEFNAKKNLIKNEFIY
>NZ_CP015199.1|WP_066751313.1|840871_841282_-|curli-assembly-protein-CsgF
MKTLILILTFFAGIFLGKSQQLVYKPVNPAFGGDTFNYQWLLSSANAQNQFDQKNDYSDLLGNLNSVDSFSQSLNRQVLSELSRKLFEDQFGEGSIQPGNYLFGSMYLQVTTTAQGLLINILDTSTGDQSEIVIPK
>NZ_CP015199.1|WP_066751311.1|839474_840839_-|curli-production-assembly-protein-CsgG
MRAYTYTRIFFCAVMLCVIQACSSLFGLPSNPEKSTMGENTSYTAELKNLPLPKEKVVIGVYKFRDQTGQYKPSENGNNWSTAVPQGTTTILIKALEDSKWFIPIERENIANLLNERQIIRSTRQEYLKDAEKNSQALPPLLYAGILLEGGVISYDSNIMTGGLGARYFGIGASTQYRQDRITIYLRAVSTLNGEILKTVYTSKTILSTSVNGSFFRYIDTERLLEAEVGMTQNEPVQLAVSEAIEKSVKSLIVEGIRDKIWGKSVDNTVDYQALIDNYNREQEQNQNRAIGNRYPDNQRGKFSIFAQAEGQKIKDDYINPKMNIGGKLGFKYFISPNFNVEVSGNYFTLENENIVKRNYFVPEVNLEFLVFPKYKFTPYIYGGLGAMYSEFKPNYKGQVGGGLEYLIDKNVAVRASAQYDLGFKDNWEGLVNGKRKDQAMRFALGINFYIGNK
>NZ_CP015199.1|WP_066751309.1|837951_839463_-|carboxypeptidase-like-regulatory-domain-containing-protein
MKTLIQLISIIIFSVCLFSCNEELVDQAQTGILKGKVVKRGTNEPIANVKIFTAPTTQTVFSGTDGSFEIANMPVGNYSVKAELSGYLTNFQAVNVQNQNQVVTVVFEMDDDESLNSPPTTPVLLSPVDNAVNQPLSVELTWNATDPDTTDVLKYSLTVKNNLDTNVIQVNDLTAKHYSLSNLKFGVSYFWQVSVSDGIHQPVLSSISKFTTNTVPSNRYHYAQKQNGNLVIVSSDASGNNFQFTNSSYNSWRPRKNNNAGLIAFLRTEGGSAHLYTANPDGSNLFKVTSVPVAGFNNFEMDFSWSTNGQELIYSNFNKLYKINKDGSGLTLIYTTLDGSMISECDWSYDGSKIALKTNDFNGYNVKIYIVDMVGSVVKTILTGVAGAAGGLNFSVDGQLLLYTKDVSAYQDGSGNYRQLDSRIFIYNLATNTNIDISTESDKPLGTNDLDPRFSPNNAQVIFMNTSNDNVSQKNVMTIDLSSSMTDLIRTALFSNAEMPDYE
>NZ_CP015199.1|WP_066759483.1|837109_837757_+|response-regulator-transcription-factor
MKPRLTIFDEPVLYTEGLSKLLTQSKIFNTIDVFNCYEALSIQLKKEPPEFLMISSNMLMLTELYKSVESITSENKNIKIIIIGNSYDIVDIRKLFNKGIKSYLDKNSRYDEFIKSIQALLLNEIYICDHAKDRMINFISSEHAQKRLQIKDPLTRREMEILKLICDGLSSKDICEKLFISINTVETHRKRILLKLNVKNSVGVVKYALENHMID
>NZ_CP015199.1|WP_066759482.1|836412_836889_+|OsmC-family-protein
MSKDHHYKTTIQWTGNKGTGTSNYRSYERSHTVSIENKAIIEASSDPAFRGDKTKHNPEDLFLSSLSSCHMLWYLHFCSEAGIIVTDYTDNATGIMEETTNGSGHFREVTLNPTVIITEESMIEKAKELHHKANEFCFIANSVNFPVKHIPLVLVKSI
>NZ_CP015199.1|WP_066751307.1|834742_836302_+|ribonuclease-E/G
MKKELIVSHEGDFTKIALLEDGRLCELHEEEDKSDFIVGDLFIGKVKKLAPNLNAAFVNIGYDKDAFLHYQDLGPQYLTYKKFLKDTISKKQSTSSLKSFEIQPEIDKNGTVEKVIVKDDLVLLQITKEPISTKGPRISTQVSLTGRFLVLIPFDNKVSISKKIKSYEEKERLRTLIESIKPEGFGVIIRTVAEGKKVADLHNDMNQLIQKWESTFKNIQKNKFPSKVLSEEDKASAILRDNFNQDFVSIICDDEQMVEEMKNYVEVIAPERKNIVQFYDSHIPLLEYYNVEKQLKQSFGKHVNIPSSKGAYLVIEHTEALHVVDVNSGNNITTGNAANKEHALNVNKMAATEIARQLRLRDMGGIIVIDFIDMPNPDHRRDLFEHLKAEMMRDKARHKILPPSKFGLIQITRQRNRQEKQIETKEDNPNKDGEIIAPIVIVERLEETIRNIIQKDKGKLYLHVHPFVEAYLTKGIKSIQMKWFIKYKKWVTIIPRDSFKYLEYKIYNSKKEELIGYSN
>NZ_CP015199.1|WP_027388329.1|834076_834367_+|integration-host-factor-subunit-beta
MTKAELVNTISNKLGTEKNETQKVVEAFMQEIRTSMYNGDNVYLRGFGSFIIKTRAAKTGRNISKNTAIEIPAHNIPAFKPSKSFVEKVKTKVTVK
>NZ_CP015199.1|WP_066751305.1|833265_833937_+|response-regulator-transcription-factor
MSKLLTNTVRFSIADSDFYFKKIMIKTLMENPFYMLLNDCNNGHEIVNRIYRRQEDVFIIELFMPVLSGIEAIKYIRKSNSETPIITYSGTYQEDMAEILSKIPNTFYCQKKSSVIKDIVKGQIASNTFDYEAYSKEWEQQPLAVQEYMDRQKQSQGELSSTEIQLMKFCYEGFSNKEIGEKLNLSTRTIDTYINRLTEKLGLKTKLHLIRFCVENGYYNSSM
>NZ_CP015199.1|WP_066751319.1|843712_844342_+|CoA-pyrophosphatase
MENFGKDLLRKIKSVELPGEHAHGVFSPPSRPVFTYDEVLAKNPKFAAVNIILYIKDDEWYFPLILRTENERDRHSGQISLPGGKREETDRDFAETAVRETSEEIGIEKHYVRIIREMSPIYIPPSNFYVYPYISYTKKDPKFILQHTEVVETIEFPITSFLNLPDKPEIMALPSAGGHEVPVINFNGYIIWGATAMILSEFSQLLKKM
>NZ_CP015199.1|WP_054511251.1|844369_845176_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MAKKNIFTDAFGTPYFLKRLIIFILGLVSYRRFNGFNKLKITGTEHLVDLPDSNVLFVCNHQTYFADVAAMYHAFCAVNNGYLDTIKNPIYLLNPKIDFYYVAAEETMNKGILPKIFKIAGAVTVKRTWRAEGQNVNRMVDLTEVDNIMKALDNGWVATFPQGTTSAFAQGRRGTAKLVKNQRPIVIPIKINGFRRAFDKKGLRVKVTGVKPTMEFKAPLDIDYDNEKAPEILLKIMTAIEQTEDFNVLHNYDEELKAKKLEQKDSDN
>NZ_CP015199.1|WP_066751322.1|845188_845626_+|hypothetical-protein
MKRIIGILFAIIVLVSCNSQKVYSDFDISYSKNGGPSPIYENLLIKANNVHYSFEGQGKKIKKEFKLTNEDLKKLDNVLSQNNFRRIQEDRKKLYDNVTTSINVKKGPNEGSKTDASLVMPNYKTNWDNILNAFQEIINNNVKKQ
>NZ_CP015199.1|WP_066751325.1|845631_846969_+|peptidoglycan-synthetase
MNTHFIAIGGSAMHNLAIALKDKGYQVTGSDDAIFEPSKSRLEKKGILPQEMGWFPEKITSDIDAVILGMHAHQDNPELAKAKELGLKIYSYPEFLYEQSKTKTRVVIAGSHGKTTITSMILHVLNFHQKDVDYMVGAQLEGFDCMVKLTQDNDFMVLEGDEYLSSPIDLRSKFLLYQPNIALMSGIAWDHINVFKTFDDYIEQFRRFVASITPGGVLVYNEEDAEVVKVVETAENYFRKIPYKTPEYEINNGQVYLKTEMGDIPLSVFGAHNLLNLEGARHICHTLGIMDEDFYDAIMSFKGASKRLEKVEREDKGILYKDFAHAPSKVKAAVKAFCEQFKNEKKYGFLELHTYSSLNPVFLEQYDHAMDGLEEAIVFYSEDALKIKRMDPISPDLIKEKFKNENLKVFTNAEELHAYWETLDKTNGVFLMMSSGNFGGLDLTK
>NZ_CP015199.1|WP_066751328.1|847098_847974_-|aldo/keto-reductase
MQKKTYTGQPVITLNNGVDIPALGFGVWQIDDQKVCEDTVIKAIQTGYRMIDTAAIYQNEVGVGKAIQNSGVNREDLFITSKLWVQDTTYDKATSAFHRTLDRLQLEYLDMYLIHWPYSDFIGAWKALEELYHEGKIKAIGVCNFTVEKLEELKANSSILPVVNQIELHPIFQQKELQVYNRENNIVTQPWSPLGNGNAELLNNESLKAIAEKHNKTVAQVILRWHLQEGFCAIPKSVTPSRIEENFNVFDFELSEDEMNIVRSLDTGKRLFFDPKDPEWEQKMLNVVVDI
>NZ_CP015199.1|WP_066751331.1|848213_849809_+|T9SS-type-A-sorting-domain-containing-protein
MKINYKKMVPFIGILCSSAITAQAPAIEWQKSLGGTNSDRAHTIIQTADGGYMISGASNSNNGNVTGNHGNQDYWLAKLNATGNLQWQKSLGGTGTDYGSSIIQTADGGYVVAGTSDSNNGNVTGNHGLTDGWVLKLNSDAGIIYWQKSFGGTNYDVINQMIPTTDGGYIFAGNSSSNNGDVTGNNGYVDYWIVKINADGNLQWKKSLGGTGDDRAISIVQTNDGGYAVAGYAENNNGDVIGNHGGKDYWILKLNTDGGVIFWKKSLGGSHQDLAYSIKQTSDGGYIVAGNAFSNDGDVTGNHDGTDAWIVKLNSDGNLQWQKALGGTKVDDASSIIQTADGGYLAVGSTTSNDGQVTGYHAPSSTGPGEAPLSYDYWAVKLNATGSIQWQKCLGGSGSDEASSVIQTADGGYVIAGSSNSNNGDVSGNHGDYDIWVVKLAQDNLATNEVLKDDIKVNIFPNPTKDNITLKLDYSTPSMEVTITDMLGKIIHTQKLEGLTTKINTNNLKKGVYFLNLIGGKENVSKKFIKE
>NZ_CP015199.1|WP_066751333.1|849961_850903_-|LysR-family-transcriptional-regulator
MVNLEWYRTFKAIYKTGTLTGAAEALFISQPGVSLHLSSLEAYVGYKLFDRTGRKMHPTERGKVLFNAVSDPLTKLEDVEKNFQKSTEKTTPTISVGMCFETFQTTLEQYVSSLPFNLIISFGEYPEMLDQLDKGILDLIITPKKGISPNIQHEAFSSEQIILVGGKDVDTESFKKVLKTKDKEQIESWLKEEKWYGTTGDMEHLFQFWTLNFGHKPDFRANYIVPNLNSIIRCLKGGKGLAVIPDFLCKNEIENGEVKLIWEGEKKLENTLYFGCRKNTSYQSEIAHIKGLFRQVMSKDAFTADSQISMILE
>NZ_CP015199.1|WP_066751336.1|851040_851781_-|metallophosphoesterase-family-protein
MQIAIFSDVHGNLPALEVVLNDIEERGIHQKFCLGDLVDFAPWGNEVIEKIKNLNIPCLMGNHDERIAFDIPVIPLTKHSEEETAARFLAIDHSKKYITKENKKYLSELPFHLKLNYKIGKKHWNIQLVHSSLKSNDTYLYESENDNIFIDLLNDSQSDVVIMGHTHLSFKKYFDGKWAINSGSVGRSREENRLASYVILTLDEDNITPEIIQLEYPLEEVAQKIEESEIPNYYASFLRNEKLSVF
>NZ_CP015199.1|WP_066751338.1|852130_852745_+|NAD(P)H-dependent-oxidoreductase
MKKVLIINGGQNFGHSGGKYNKTIADSTLEVLQKFENVEVKTTTIDEGYNKDEEVQKFVWADVIIYHTPIWWFQLPNGFKKYIDEVFTAGHAKGIYMSDGRTSDNPQTNYGTGGMLGGRKYMVTTSWNAPETAFTLPGEFFNETSVDNGPLFGFHRMNAFVSLEKMESFHFHDVEKNANIERDMKVYKEHLTNIFEQELKPQLA
>NZ_CP015199.1|WP_066751340.1|852744_853032_+|antibiotic-biosynthesis-monooxygenase
MKIYLTAVIKAKEEHRTEVLEVLQNMVSETRKEEANELYTLHQGIEDKNHFIFYEIWKDQEGLTQHNQQPYIQAFGDLVDEKLQEKPQIYLTNII

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Crispr_ID: NZ_CP015199_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP015199_2

4718560-4718783

Orphan

Consensus_repeat	Method
ACCTGTATCTCTTTTACTCAGGT	CRISPRCasFinder

3 spacers

The CRISPR arrays of NZ_CP015199_2

>merge|NZ_CP015199|2|4718560-4718783|CRISPRCasFinder
ACCTAGCCTTTTTTTACGCAGGTTGACCTTGTATTATTTTACACACGTCAGCCAGGAACCTGTGCCTAACTTACGCAGGTCAATCGAATACCTGTATCTCTTTTACTCAGGTTGCTATTGTGCAGGAAAAATTCCCAACCTATATCTCTTTTACTCAGGTCAGCTAAGAACCTATATCTTTTTTACGCAGGTCGATTGACTAGCTGTATCTATTTTACACATCT

>NZ_CP015199|2|2|4718560-4718783|CRISPRCasFinder
ACCTAGCCTTTTTTTACGCAGGT	TGACCTTGTATTATTTTACACACGTCAGCCAGGA
ACCTGTGCCTAACTTACGCAGGT	CAATCGAATACCTGTATCTCTTTTACTCAGGTTGCTATTGTGCAGGAAAAATTCCCA
ACCTATATCTCTTTTACTCAGGT	CAGCTAAGAACCTATATCTTTTTTACGCAGGTCGATTGACT
AGCTGTATCTATTTTACACATCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP015199.1\|WP_066759159.1\|4703002_4707049_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_066759173.1\|4716141_4717131_-\|site-specific-DNA-methyltransferase	unknown	unknown	gnl\|CDD\|334588
NZ_CP015199.1\|WP_066759167.1\|4710569_4712771_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|131694
NZ_CP015199.1\|WP_066759161.1\|4707070_4708822_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_066759175.1\|4718924_4720625_-\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225117
NZ_CP015199.1\|WP_157886092.1\|4720898_4721327_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_157886093.1\|4721607_4721922_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_066759165.1\|4709669_4710563_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|131694
NZ_CP015199.1\|WP_066759171.1\|4714113_4716132_-\|DUF87-domain-containing-protein	unknown	unknown	gnl\|CDD\|223510
NZ_CP015199.1\|WP_066759155.1\|4699354_4700107_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_082891219.1\|4723344_4726524_-\|SusC/RagA-family-TonB-linked-outer-membrane-protein	unknown	unknown	gnl\|CDD\|274948
NZ_CP015199.1\|WP_066759169.1\|4712767_4714108_-\|DNA-double-strand-break-repair-nuclease-NurA	unknown	unknown	unknown
NZ_CP015199.1\|WP_082891221.1\|4731411_4732449_+\|nucleoid-associated-protein	unknown	unknown	gnl\|CDD\|377262
NZ_CP015199.1\|WP_034706501.1\|4717878_4718139_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378935
NZ_CP015199.1\|WP_082891220.1\|4726582_4727884_-\|TlpA-family-protein-disulfide-reductase	unknown	unknown	gnl\|CDD\|239264
NZ_CP015199.1\|WP_066759182.1\|4721983_4723333_-\|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	unknown	unknown	gnl\|CDD\|185760
NZ_CP015199.1\|WP_066759163.1\|4708869_4709667_-\|HNH-endonuclease	unknown	unknown	gnl\|CDD\|225973
NZ_CP015199.1\|WP_066759192.1\|4728912_4729965_+\|nucleoid-associated-protein	unknown	unknown	gnl\|CDD\|377262
NZ_CP015199.1\|WP_066759194.1\|4729970_4731467_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP015199.1\|WP_066759190.1\|4728503_4728752_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP015199.1\|WP_066759173.1\|4716141_4717131_-\|site-specific-DNA-methyltransferase	gnl\|CDD\|334588	pfam01555, N6_N4_Mtase, DNA methylase. Members of this family are DNA methylases. The family contains both N-4 cytosine-specific DNA methylases and N-6 Adenine-specific DNA methylases.	2.42182e-25
NZ_CP015199.1\|WP_066759167.1\|4710569_4712771_-\|AAA-family-ATPase	gnl\|CDD\|131694	TIGR02646, Hypothetical_protein_SMc04429, TIGR02646 family protein. Members of this uncharacterized protein family are found exclusively in bacteria. Neighboring genes in various genomes are also uncharacterized or may annotated as similar to restriction system proteins. [Hypothetical proteins, Conserved].	3.08519e-11
NZ_CP015199.1\|WP_066759175.1\|4718924_4720625_-\|AraC-family-transcriptional-regulator	gnl\|CDD\|225117	COG2207, AraC, AraC-type DNA-binding domain-containing proteins [Transcription].	5.80884e-09
NZ_CP015199.1\|WP_082891221.1\|4731411_4732449_+\|nucleoid-associated-protein	gnl\|CDD\|377262	pfam04245, NA37, 37-kD nucleoid-associated bacterial protein.	2.93897e-26
NZ_CP015199.1\|WP_066759182.1\|4721983_4723333_-\|RagB/SusD-family-nutrient-uptake-outer-membrane-protein	gnl\|CDD\|185760	cd08977, SusD, starch binding outer membrane protein SusD. SusD-like proteins from Bacteroidetes, members of the human distal gut microbiota, are part of the starch utilization system (Sus). Sus is one of the large clusters of glycosyl hydrolases, called polysaccharide utilization loci (PULs), which play an important role in polysaccharide recognition and uptake, and it is needed for growth on amylose, amylopectin, pullulan, and maltooligosaccharides. SusD, together with SusC, a predicted beta-barrel porin, forms the minimum outer-membrane starch-binding complex. The adult human distal gut microbiota is essential for digestion of a large variety of dietary polysaccharides, for which humans lack the necessary glycosyl hydrolases.	1.4398e-26
NZ_CP015199.1\|WP_082891220.1\|4726582_4727884_-\|TlpA-family-protein-disulfide-reductase	gnl\|CDD\|239264	cd02966, TlpA_like_family, TlpA-like family; composed of TlpA, ResA, DsbE and similar proteins. TlpA, ResA and DsbE are bacterial protein disulfide reductases with important roles in cytochrome maturation. They are membrane-anchored proteins with a soluble TRX domain containing a CXXC motif located in the periplasm. The TRX domains of this family contain an insert, approximately 25 residues in length, which correspond to an extra alpha helix and a beta strand when compared with TRX. TlpA catalyzes an essential reaction in the biogenesis of cytochrome aa3, while ResA and DsbE are essential proteins in cytochrome c maturation. Also included in this family are proteins containing a TlpA-like TRX domain with domain architectures similar to E. coli DipZ protein, and the N-terminal TRX domain of PilB protein from Neisseria which acts as a disulfide reductase that can recylce methionine sulfoxide reductases.	2.12323e-11
NZ_CP015199.1\|WP_066759165.1\|4709669_4710563_-\|hypothetical-protein	gnl\|CDD\|131694	TIGR02646, Hypothetical_protein_SMc04429, TIGR02646 family protein. Members of this uncharacterized protein family are found exclusively in bacteria. Neighboring genes in various genomes are also uncharacterized or may annotated as similar to restriction system proteins. [Hypothetical proteins, Conserved].	1.87823e-10
NZ_CP015199.1\|WP_066759171.1\|4714113_4716132_-\|DUF87-domain-containing-protein	gnl\|CDD\|223510	COG0433, COG0433, HerA helicase [Replication, recombination, and repair].	1.00586e-10
NZ_CP015199.1\|WP_082891219.1\|4723344_4726524_-\|SusC/RagA-family-TonB-linked-outer-membrane-protein	gnl\|CDD\|274948	TIGR04056, OMP_RagA_SusC, TonB-linked outer membrane protein, SusC/RagA family. This model describes a distinctive clade among the TonB-linked outer membrane proteins (OMP). Members of this family are restricted to the Bacteriodetes lineage (except for Gemmatimonas aurantiaca T-27 from the novel phylum Gemmatimonadetes) and occur in high copy numbers, with over 100 members from Bacteroides thetaiotaomicron VPI-5482 alone. Published descriptions of members of this family are available for RagA from Porphyromonas gingivalis, SusC from Bacteroides thetaiotaomicron, and OmpW from Bacteroides caccae. Members form pairs with members of the SusD/RagB family (pfam07980). Transporter complexes including these outer membrane proteins are likely to import large degradation products of proteins (e.g. RagA) or carbohydrates (e.g. SusC) as nutrients, rather than siderophores. [Transport and binding proteins, Unknown substrate].	9.10162e-145
NZ_CP015199.1\|WP_034706501.1\|4717878_4718139_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|378935	pfam12728, HTH_17, Helix-turn-helix domain. This domain is a DNA-binding helix-turn-helix domain.	5.61068e-07
NZ_CP015199.1\|WP_066759163.1\|4708869_4709667_-\|HNH-endonuclease	gnl\|CDD\|225973	COG3440, COG3440, Predicted restriction endonuclease [Defense mechanisms].	1.61197e-15
NZ_CP015199.1\|WP_066759192.1\|4728912_4729965_+\|nucleoid-associated-protein	gnl\|CDD\|377262	pfam04245, NA37, 37-kD nucleoid-associated bacterial protein.	2.6463e-12

>NZ_CP015199.1|WP_034706501.1|4717878_4718139_-|helix-turn-helix-domain-containing-protein
MRVNLVTKEDLQEFKTELLEDIKNLFNIKISEQKLWLRSSEVKELLKISTGTLQNLRVSGTLSYTRVGGTLYYNYKDIEKMLNGKG
>NZ_CP015199.1|WP_066759173.1|4716141_4717131_-|site-specific-DNA-methyltransferase
MSIGEKLTQKYKSKLGKLFVGNSLELLTNDKKLSKLKGKVNLIVTSPPFPLNNKKQYGNEKGDEYKDWFIKLAPIFSDLLTDDGSLVIEIGNAWEPERPVQSLLHLECLLGMVKHPEANLRLIQEFICYNPSKLPSPAQWVTVNRLRTVDSYTHVWWIAKNDFPKADNSKVLRPYSDSMKQLLKRQSYNSGKRPSEHQISEKGFLKDNGGSISHNFFEMEALEEKREVRLPHSVLSFSNTNSNGYFLKTCRDKGITPHPARMSGGLVNFFIQFLTDEDDLVLDPFSGSNTTGYCAEKLNRKWISFEIKEDYIKQAIIRFSDPELKSPLK
>NZ_CP015199.1|WP_066759171.1|4714113_4716132_-|DUF87-domain-containing-protein
MKTVDKIKQLVSVDPLKVGKQTELFVGHPFSLDYNKANILVCDADKERVKGIAQGTFLLAFYDNEETVEEAILLRALAPAKLPTDSAMISSMIEYYKDNLPTSGKSSKLDDFTRYEFSFSGLECRVLGTFYRNGNNVEFGADLENFYSAHHYSVYKVNKDVLGYIVNQRDSPDIIPGNDNEFSIGHVRYSSSLRFQSKNEEDKAEVYIHPADLLGKRTALFGMTRTGKSNTVKKVIEATSQISSKATATLPSKSPNTIEENLKSFDTNGAPKYPVGQLIFDVNGEYANKNLQDEGTAIFEKYKTNTVRYSILEKSDADFKIMKVNFYKDIVTGFSYICASLEDEKGDYITSLKVLDFTPPPLDNEHFDEWTRYNKNKAIYFCCLNKAGFNPSTNFTVKFKADATIKKLVSEKYKELDIEKGVSLDEAESWFLCAWENINDKVFTDYKKKKGKDWFSDEMKSLMIFLTQKKDGRSVSGFDKFKKVAKMHTNTTENSFEVDISKHLRKGGIVIIDLSQGDPKLQEIFLERISKKIFSDSMSRFTDSLPNNFIQFYFEEAHNLFPKKDDKDLSQIYNRIAKEGAKLNLGMIYATQEVSSISSNILKNTQNWFIAHLNNEDEIKELRKYYDFDDFADALIRFSAKNDKGFVRMKTYSNPFIVPVQIDKFSVEISTK
>NZ_CP015199.1|WP_066759169.1|4712767_4714108_-|DNA-double-strand-break-repair-nuclease-NurA
MAYSSRTGKRPDELASKSSHSFLINDEEVQSFLENCEYPKSAEEVELDRSRIIKIQYPEENSIEHIIAMDGGYSTIPVRKTFPSSLITFFQFGEIFLNTEDLNNMSEMPFISRESMSALKDLERSKLVLPTKNVSYNSNITLTHSVRSTIYEYFKKKGDEKNNLLSTTYWLIFNLFDQPEESFNLTICPHCKGKNQDILRANFNSEYTTNCPECNGILYLTDCFRLHEVIDDELGAGGILGYLVNLIEQINIIHTIKYIKETQPKLLDKFFFIKDGPLAFFGQTANMHKHVRKLCNYLFEHHNLFLAGLEKSGAFVEHADEIKNLLEPGEALLLTNKHIYSYILPGDPENTQPYAGTSYYSSKIIFKSRDERVYVITLPVENENIVLNPQKDDFKNLDTILWNIEKLRCDMYDNSIVPVALANKLISLSSHPSSSILEKFAKKHTK
>NZ_CP015199.1|WP_066759167.1|4710569_4712771_-|AAA-family-ATPase
MIYVERNIIPVPKVFYSKEVEIAKKRLEEFYLKSKESRSQQKYSQPFEKELRDKFLEALREVFKGKCAYCESPISFNRTQSEYDHFRPKGGARGLDKEFSTDHYWWLAYNWNNIYLSCSHCNQYKSTWFPVEGKRIPLNTPYKEVVDNEKALLIDPCIDKPEEHLIFNEQGGIEAISSKGITTIEILKLDRSELVNSRLEALKELYGEWELLLKLLRKKESNRDDIKKLYDAWQYKYTIHSGEPYLGIQRFMLSKWLGNRPEIQEYLSTIDGKETKTPVNTLAQDFLYSKAENFKETEKDNIEQSISSIKHIYVEKIELKNFKCFSSLELEFNHNSDSLIGNEPWLLFLGENGVGKSSLLKAFVIGLTGDEYIKSLELKGRDLLKHGARNGFIRIHLVGAIRPIEVTFNKTEIKTTLHQPIVNIVAYNSIRLNPKEGKIQPEKGDFYGAKAKNLFDYTFSLIDADTWLVKLFKKDKDAFDRVAISLKDLMLLENDDTISIIKNQPIIKRNGDVFSIDELSDGYRSIFYLAVDIMATLAGENVTFDLAEGMVLIDEIGTHLHPRWRMEVVTRLRKAFPKIRFVVTTHEPLCLRGLRAGETVVLTKNQENEVIALTELPDPSELRVDQILTSDFFGLKSTIDPETERLFDEYYLILALEENDRTEEQKNRLLDLSQIIPRIKHLGDTEREELTYYVIDELLARRTREDGPKIKEELKAEALKRVESIWKTLDTKK
>NZ_CP015199.1|WP_066759165.1|4709669_4710563_-|hypothetical-protein
MIKVDRSQVSKPSALDKKNKAGKTETERAIEHYTSPTFDGTTNFDFKIYSDSEVKQALINLFKGKCAYCESTFLHVYSGDVEHFRPKGEIEEASPHKKPGYYWLAADWHNLLLSCRNCNQKLSHSLYGIGTKKTMGKMNQFPLSDLTKYVRKHDNVNGIADEEPHRLLLNPCIDNPEDHLEYGDEGVIRPKKDAGGNKSVMAEKSIDVYVLQRMYLVQSREKKLIEMQAQIQRVKEATENYNDIIGSPDTTKKFYFERILKREMEGLKKFLNPKEEYVGMARQVVGEFLRVNFGITI
>NZ_CP015199.1|WP_066759163.1|4708869_4709667_-|HNH-endonuclease
MNWVKENRNKLSINNYVRKADAKTNYWLDLSEGRINNYRKLTNDNFNIIIYGNDNLETDFYIIPFEELKHLLLENNFAKSEGRRRWIGNIINHHISLSNTGVKLNISHRYSNPIPFKVEPLILNIESTNDYAIENAKREIQVRIKQSAFRKKVLENFDYKCCLTGIIENDLLVASHIIPWASKIDTRLSPHNGLCLSTLYDSLFDKGYFSIDEKYQVIITPKLDELSLQTQNWLSEISGKTISLPLNYEISTVALKFHREKVFIK
>NZ_CP015199.1|WP_066759161.1|4707070_4708822_-|hypothetical-protein
MKLTGKIVITFNDIFPDEEPKSINEYLDGIDKDLLLKFGTFLLGFSQNSKYENPLEFLKMYFSQENQEFFNKVLSGLDQFIKQTKWEIESYSFPYVASSLSFFENAFDKEYEITKNYTNQEIEIRVFKAYLLFNKFNTTDRTLILNDSLKYLKGDRSKYATAYCIGLFLNNSDLVNYDIKKVFTTQVLRAISFFEFLESRNDTRELLKEFYKEYDISNYQEYIKRLLPIQIAVLKKEKESHIDIDITQNDGKESSISFLNKFSIKESELLKDFDFKNIRSSPMYRFDEKTFRLIFPLFVLELIGNGLYFKFKHINDRLAKEKKAKDLYGLKTYDFSEKYILHKILKEYFGNRYFQKNGDELDAQYDGAPDYYVRNGKKIFLFESKDILINAIAKQSSDFSKIEKEMSIKLYKNEEGKPKAVLQIINNIRKILSKKLEFDSNYNTKNLIVYPILVLHYRIFDTAGLNKWVNFWFQEELNKLGKEGFYTSNIKPLTLIDIDTLIFHKEVFASRKLSLEEVLNEYGNDYINFTAKGKKYRSEEDVIQASKNSFIPFGHYLDNKIDLKKLREVPKEFMEKTYGLLNK
>NZ_CP015199.1|WP_066759159.1|4703002_4707049_-|hypothetical-protein
MYYKNKEKIEAIQNIIKPFEIDRNHNKNDKALQADIYWNASIFFAKILIKAVIQKNYCSKEDVEKFSKKYNTENNTSIDIDSLFKKFWLREILGIIHIPDAVRKVIYDFEKNQSYKEELRFVREVYKTYQTKTTNKTEYQKFIAQYKIKNNVNLDKEWLSTNWIKTSKKSKDDIDVGNIIYYSVLLDNWDEFEFLYKLKKNKLEYNSKGLELSKKNFNAIHTAHQLYFIKAPSIDDLKEQRIIKEIDNKYYINFYDCEISYWGTLSDTIGGFVWEDLISDDKIPDDKERVIIFVRKMLYWENSWSDFYKHITKESKNRFIKSALELILEEQDIVGVENEFFKCFIDESVGSRYAFQGGIDLVEEALKPSTNYYELYEHMRFLSKKHQGNLFYIQEVRNDLAFLIKTIVCCDNPFSKTKGSDSEKIEHYPLIKSLLENSLSKPYLLWETCHFLIQDKPTIIPYLMEVPYFSTLAFSLVDKLKIESSIAEINRSIKFKLIEDSIKLSLDSILSSQKHTNKEIALLIFQFYKEINKDKYQSLSNVRREEDVYEIREYQKKKEQLLISIIEDCRVNGFDTYNSSSEFLLPKIISELIEIFKNYEEPILYLNGTIQFPILVLDGLSWLSKCSIYSKYEKQIQDIEDIREILSDSFKEIYLDKIEQKSVQKKDFQSNNIIESLPSWAERNERLNLIDWVYPVALLSDSEKLKEFLSPRINLKKAEHEYDEENRFNASKIRTHLFVLLTVLKKITTNKAEYFLIYDKLKDVKISIEQNILDLLKQYAVVGKPSKIDILSSSFEQKVFRASKEEELLPQVAQAINWFGDKNKVITILIDTSDLLRLLIILDWVTSEGIKKEIIERIKKAKLIDFFKSQSWIPEIELTLSKLSHYKELIVQTEEALDYWEKNITSKRNEIEYKQASFVVRLMLAYNQKDIQQINNLEEPGKNAFEVRGFKPYDYKQFFIGLIHFEDKPKEAYKIFDRLYNQFKESSSVCINRFAAKINWATKNDDIIIKNKLLNESLEEWEDAGKNLSEQSIESIIDKVWVNKLTVYYHLKNVTEFEQLFLSLPDPYQMMEEVAKMRIELFLEHIKQQEAIYYLNKVKEYHKFSDGSNLDFINELSSLVDDKSNIELLKASYNEIFSKKPQTLIKIFPEKLNGQIDIGNFIAKEFAIATNKALDKILSIDEIKNEDKYNDLVQICLESRFSVFGWIVKDQTRGAFSGRGLHPGERDILIQNSNSETILVCEAFIYRDVRTTQSHLKKIFNYHHQKENLLVLIYDLGLSSNFENKWKKYLKETLPKLNYPTDFEIDSSKTKDLTDNLNYKASAIKIAMTFHGKSTTIHHLMINLKYKI
>NZ_CP015199.1|WP_066759155.1|4699354_4700107_-|hypothetical-protein
MRKIKLHFYAVVFIAGIKVHGQVGVGTASPYPSAVLDLNSSKKGLLLPRIALTSTADITTVSNPAKGLLVYATQNAGTGITAIQKDTLYKFDGTNWKAFTTREKFIANELPKIVAVGRKTTTEPCTAATTNGLFNLNVRSSTSITATGAFTAPQAGYYMFSVRIIQLMAPSPSQPFNASPYIQAQNLATYSYLYRGSGPSAQPASVLGVIYLASGASTQGFRWFLGNNTCTTDSRIQGQEVTWEYLGNPL
>NZ_CP015199.1|WP_066759175.1|4718924_4720625_-|AraC-family-transcriptional-regulator
MHYHHKISLLIFNLFFFFLNAQELQSLSYKTISDLYENYPENDSRAMVFVNKYIEKAKKENNWKKQIIGYEDAIYYTEDINRKLSYADNAIVVAFKLSDRDIISRAYLGKGIVYYYNKRQYKYALEQYLKAYQFSRNSSDDYLINKIDYHLGMVKSYLGYYEAAAVHFKNTTKYFEESMKENLHPNIRLNNESGYFNSIYRLSNCYENLRLYNKEDSLISIGLQKLKNINEHLLEYGYFQKGKGVQLLRKGNTDEALKHLKLSRDILVNNQDYNSLTAVYFYLGKLYWLKGNRAESLVYLNKVDSMINKVQFTTPEIRSSYKYLITDATENGSLGKRLYYSDQFLLTNSTLNVDFAMLSSKIHEEYDTERLLEEKQLLENKLRNDFYFLVATPVIFVLLFFLVIKLRNRERKFPGKFIKLWKKFRKYYSFLIANKKTSEKKKTHNPEIIDDIKEKLKKFEEDRRFLDKNLTLPMVAKMFGRTHSQLSYVLNEHLNVSFTQYLKVLRIKYITALLLENDLYLKYNIENLAHECGMSSRQLFSTHFLEINGIRPIDFIKNRMKEIDEN
>NZ_CP015199.1|WP_157886092.1|4720898_4721327_+|hypothetical-protein
MKKVKTRVVEFISYFFILLFCYAGISKIMDFENFQIQISESPLLSAYAAFLPFAIIILELIIAGLLCYRKTRNTGLIGSFILMLIFTGYIFFIIHTSENLPCSCGGILEKMSWNQHLIFNIGCVLLDAIALIMNIKYSRPAR
>NZ_CP015199.1|WP_157886093.1|4721607_4721922_+|hypothetical-protein
MKFNQFLKMNAVAIAAVMFTGATMSFKIIEKKTADQQFYYNSTDTSAGAFSQESNWAVGAGSSCLTTGNKPCTISVPEGQDLVDVIGGMTNSQVLAIHPSERRQ
>NZ_CP015199.1|WP_066759182.1|4721983_4723333_-|RagB/SusD-family-nutrient-uptake-outer-membrane-protein
MRKIKILVISLSLILTSFGCSDFLDEKSDLKLATPDRLEDNQMLLNNYGFLNVDFASSGETSSDDYYLTDADYYGLSFEASKRLHIWMPDNVASPISSGNDWSTCYRSIYVCNAVLFNMQDKNFTGEQADNIRGQALALRAFRYLDAAQIWCPAYNPQTAGTDLGLPLRLDPDMNIPSVRSTVKQTYNQIISDLQTAIPLLLPKQISGMRISRAAAYGLLARAYLYIGDYNNALKNTEQALNINNDLMDFNILNPNADYPIEEMNKEVLLWTAMGYESHLIPAKIPDHIYQMYDNNDLRKTVFFNKNTANEVLFKGYYNNVNGPIVSVATDELYLMAAECNVRLNKIQEGMSYLNNLLVKRWKTGTYIPMTANSQAEALNIILKERRKELLIRGLRWSDLKRYNRDGANITLTRTVNGQTYTLSPNDLRYAIAIPEDIITLTGMPQNPR
>NZ_CP015199.1|WP_082891219.1|4723344_4726524_-|SusC/RagA-family-TonB-linked-outer-membrane-protein
MKKLLVLPILCYCVPIMAQQMFTGSVIDETTRLPVMGATIAIQNSKTVTTTDKNGKFSLSTNDKKINLVILGKGYEEQVIILELPLKETLKINLSEKIAQIDEVVLTTGYQKIPKERSTGSFSSVSNSALNTQVSINILDRLAATANGIVINKGTSQGGAQIMVRGLSTIQGPKTPLIVVDNFPYDGDISNLDPNIVENITVLKDAAASSIWGARAANGVIVITTKTAKYNQPVTVNFNTYLMTSPKPDFNYLKVMSSADFIDVEQELFKKNFYNTDINSTSHPVLSPVVDLLNKEKKGLLSSEYVRNEIERLKTIDSRDQYRKYMYQPLENRQYSLSMAGGAPQFSWTSSLGYDDNTGNLGEKYERVNLRFQNTWQPLKNLTLNTGIFFTHSATQNGRSAYGSIIMKTNSVPYMEMADKYGNALAVSKSYEQSYKSALGNGKLLDWNYYPLTDWQHNSAKSKSSEIILNAGLNYKILKGLDVDIKYQYQRTTGLSNTLYDEESYFVRDYVNRFTVINSNGSLTYNVPKGAIMDKNNSQLLINNFRGQLNFNRGFGKHQISAILGSEVRDANSQSGNNRYYGYDPNNLSFGMVDLSKRFPIIAGGTAFIDNMNSLRESTNRFVSVYANAAYTFDNRYTISGSARRDASNLFGLKTNDQWNPFWSTGISWNVANEKFYSVSWLPNLKLRGSYGFNGNINPAMVAVTTMALLGVSTYTQEQMARFDNYYNPQLRWETIRMINAGLDFATKNNRISGSVEYFQKKGENLFGQVPLDYTIGLSSLVWNVAGIEGKGVDVELKTININKSFRWLTTLNFSTYKDKVTNYYPSSTIARNFVLASVPISGIEGLPVYSMFGYQWTGLDPQTGDPRGYFNGEISKDYAKIMGADVKELQYFGSAIPTVYGSFTNTFAYKQLSLDVGITYKMGYYFRRPSINYTSLFREWNGHSDYEQRWQKPGDEAFTNVPSNQYQTNSNRDAFYAGSAALIEKGDHIRLQYINLGYEISKKQWRGLPIKSLQLYANVGNLGILWQESKSGIDPDFNLGNNTLKPPMTCTLGLKAKF
>NZ_CP015199.1|WP_082891220.1|4726582_4727884_-|TlpA-family-protein-disulfide-reductase
MKNIFCRGLMSFVFIIVFTTTSYAQNKSLKIGESLPESIWTNPFPVVNHSRKATNLSEDKNKLILIDFWSTWCSACLMSLPKIEALQQKFRDRVKILPVSSQDRFALDKFFSSPNGKKYKSMMSTYEDKALHELFPHAGVPFIIWIKDGKFFNSTDAGQLTEQTINEVLSGDKSSLQTIIQMNRERPLMLSDDYDRQKNVQLLNYSFFAKGKIPDIGAGGTYRKTATGKIHGRQFTNLPLWDMYYAIGYELFKRQDKTSFTEKRMVIDVNQPEQLIPIEKADGSNDGTNLYNYEFIIPEQKSDSLYNYMLEDLNRYSGYTVTLEKRPVKCLVLVRTSTKDKLATKGGEKRSTFPRTPSILRNVPLKNMVNMLNGEINIKELFIDETGYTGNVDLEVSGVKDIATLKKELQKYDLDLRPEERQLLMMIIKDQLN
>NZ_CP015199.1|WP_066759190.1|4728503_4728752_+|helix-turn-helix-transcriptional-regulator
MDEEKEVIIAICKYVYTNWISKAKSQREFASKCDIEESTVRRIKNIALGTSKTDYNMSVKTIAKICRKKEVTLEELFQNIKK
>NZ_CP015199.1|WP_066759192.1|4728912_4729965_+|nucleoid-associated-protein
MPKESVLTQAEKASAKIEKFIFHIIIESELNPFFLDEVDLTDEQLDFFRLQFLEAAEGTQFDFNDNSTSEVYKNCEKIIENPSENFFTISKDLTASFKSHHKKNMNDGVFITALVSINDSNNLIFLLKLDNRKVFEYKRTGNKAILEEIKNTFVEDKRSIQKLAIIDVTDYYKWDVLAYDRSPGVGKTISDFFRDFLVVHEKETPTTLTTNTVKAITNWTISNRADLDPVQEISSYKNRVIDYLTNCSMVDFKKLIDRVIDDSDSSRKRKLKKSLKEFLEDLGLYGQSFKPSRSVLNTAQKKNIRQTAEGIKIEWQGDANDVNIDIPNIPSSNDGFYHITIKTRDVKVVK
>NZ_CP015199.1|WP_066759194.1|4729970_4731467_+|hypothetical-protein
MDFDKLIEIIDSYDSINVKESWGYIEISCDINKRENLQKIKLLKDYLSGEGFPNSISIKIDNARVDDDDLDSYLEDDTSNWEININKIPFFNTGYIDVRQNFFYSIEKFQEWLSGLSPFEKENPFHKKNNLIINGLDHVILGDKFKIIPYKFNGNIESFVIGESLPDLNRINEVVHSLTSEELIISPLSFVYQTKSNNETIISILNKLASISLSASIVNEIKSDDFITVDGIRRLNLKLFDDHDIYKKEFYNDLLKVVKWIYEEKTITRQKLFNDRISLELDESKTYINALSIHLKNSLSQASQRYNFVILERKDKYISELKDLLKDVRSQSDLYSQKIRTLLNNLLRDVLAAIVLVGFTIFTKFSDNLLLDKISLLKYVFYFLAIYYVLSAIIQAIVDITDVQVSKNEMLYWKATTKELIPEKDFKKHIENSLKDRKRSLKILYPTIIILYLLLAYTCYKFPIYFHSISSEKTKKEKINNDKVSKYRSQQSSGSSGR
>NZ_CP015199.1|WP_082891221.1|4731411_4732449_+|nucleoid-associated-protein
MIKFLNIEVNKVAVHQVGNKSLDEQVNFSDTLVDISDERLVRIFLKYFLSSFSGNEMYDFFNEVGIEQNEIYTLIKRIFENPDDLFKQSKIIAQHLYNCSTHPKIKNGDLFIVYFNNIIIDNINTDAIGIFKSESKENYLKVDLEKKIHFVNYDEGTNINKLDKGCLVFKIDESYKVCIIDNLNKANEASYWKDDFLSIRPIKNDYHQTNEFLSIAKQFVTKQLDEEFKISKADKIDYLNRSVDYFKSHGSFDKQEFEELVFEDKGLIESFRTFDQAYRQENEIELYDNFDISTQAVKKQARVFKNVLKLDKNFHIYIHGNADLITQGIDENGRKYYKIFYEEEN

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP015199_2	2.1\|4718583\|34\|NZ_CP015199\|CRISPRCasFinder	4718583-4718616	34	NZ_CP039041	Piscirickettsia salmonis strain Psal-072 plasmid unnamed1, complete sequence	116600-116633	10	0.706

1. spacer 2.1|4718583|34|NZ_CP015199|CRISPRCasFinder matches to NZ_CP039041 (Piscirickettsia salmonis strain Psal-072 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.706

tgaccttgtattattttacacacgtcagccagga	CRISPR spacer
aaactttatattattttacacacgtccatgagtg	Protospacer
 .**.**.****************** .. ** .

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

202227 : 213441

Bacillus_phage(33.33%)

The bacterium proteins that are colored denote the protein is present at specific phage-related keywords (such as 'capsid', 'head', 'integrase', 'plate', 'tail', 'fiber', 'coat', 'transposase', 'portal', 'terminase', 'protease' or 'lysin' and 'tRNA')

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_066750191.1\|202227_204927_+	sodium:proline symporter	W8CYF6	Bacillus_phage	2.7e-18	31.1
WP_066750193.1\|204935_205298_+	response regulator	W8CYM9	Bacillus_phage	1.1e-10	30.5
WP_066750195.1\|205414_207301_+	AMP-binding protein	A0A2H4PQU7	Staphylococcus_phage	2.6e-63	32.1
WP_066750198.1\|207361_209269_+	acetate--CoA ligase	A0A2H4PQU7	Staphylococcus_phage	1.1e-82	38.3
WP_066750200.1\|209573_209939_+	hypothetical protein	NA	NA	NA	NA
WP_066750202.1\|210053_212264_+	bifunctional (p)ppGpp synthetase/guanosine-3',5'-bis(diphosphate) 3'-pyrophosphohydrolase	A0A2I2L310	Orpheovirus	1.3e-13	37.7
WP_066750204.1\|212265_213441_+	Na+/H+ antiporter NhaA	A0A2H4J5W3	uncultured_Caudovirales_phage	4.2e-72	44.3

DBSCAN-SWA_2

2113959 : 2120811

Serratia_phage(28.57%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_066754057.1\|2113959_2114433_+	macro domain-containing protein	A0A2L1IVW3	Streptomyces_phage	1.2e-33	47.5
WP_066754060.1\|2115671_2116328_+	DUF4291 domain-containing protein	NA	NA	NA	NA
WP_066754062.1\|2116317_2116827_+	O-acetyl-ADP-ribose deacetylase	A0A2K9L8X2	Tupanvirus	3.9e-27	45.3
WP_066759604.1\|2116936_2117623_+	NAD-dependent deacylase	R9TG77	Vibrio_phage	7.9e-31	39.3
WP_066754063.1\|2117622_2118573_+	ADP-ribosylglycohydrolase family protein	A0A1S6UB21	Serratia_phage	5.1e-44	35.2
WP_066754064.1\|2118557_2119523_+	ADP-ribosylglycohydrolase family protein	A0A1S6UB21	Serratia_phage	2.8e-42	35.4
WP_066754066.1\|2119533_2120079_+	RNA 2'-phosphotransferase	A0A2H4UTN1	Bodo_saltans_virus	1.7e-44	47.2
WP_066754068.1\|2120079_2120811_+	serine/threonine protein phosphatase	S0A0Y6	Cellulophaga_phage	7.9e-45	38.0

DBSCAN-SWA_3

3096807 : 3103860

Vibrio_phage(50.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_066755480.1\|3096807_3097626_-	hypothetical protein	A0A0B5HE59	Vibrio_phage	3.3e-07	44.3
WP_066755484.1\|3097644_3098448_-	hypothetical protein	A0A0B5HE59	Vibrio_phage	2.5e-07	34.2
WP_066755486.1\|3098450_3099275_-	hypothetical protein	A0A0B5HE59	Vibrio_phage	1.6e-09	45.6
WP_066755488.1\|3099547_3101206_-	ribonucleoside-diphosphate reductase subunit alpha	A0A223W070	Agrobacterium_phage	5.7e-168	54.8
WP_066755491.1\|3101266_3101554_-	hypothetical protein	NA	NA	NA	NA
WP_054510330.1\|3101768_3102743_-	ribonucleotide-diphosphate reductase subunit beta	A0A1X9I9V4	Staphylococcus_phage	4.4e-83	47.2
WP_066755494.1\|3103170_3103860_+	ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	6.3e-36	43.8

DBSCAN-SWA_4

3609628 : 3681343

uncultured_phage(28.57%)

plate,tail,tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_066756883.1\|3609628_3610678_+\|tRNA	tRNA preQ1(34) S-adenosylmethionine ribosyltransferase-isomerase QueA	NA	NA	NA	NA
WP_066756886.1\|3610750_3611794_+	23S rRNA (adenine(2503)-C(2))-methyltransferase RlmN	NA	NA	NA	NA
WP_066756889.1\|3611867_3612800_+	sterol desaturase family protein	NA	NA	NA	NA
WP_066756892.1\|3613052_3613925_+	hypothetical protein	NA	NA	NA	NA
WP_066756896.1\|3614001_3614979_+	polyprenyl synthetase family protein	NA	NA	NA	NA
WP_157886044.1\|3615050_3615821_-	hypothetical protein	NA	NA	NA	NA
WP_066756909.1\|3616227_3616521_-	hypothetical protein	NA	NA	NA	NA
WP_066756911.1\|3616658_3619091_+	transketolase	NA	NA	NA	NA
WP_157886045.1\|3619254_3619527_+	hypothetical protein	NA	NA	NA	NA
WP_066756915.1\|3619531_3619921_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_066756918.1\|3620053_3621115_+	NADH:flavin oxidoreductase	NA	NA	NA	NA
WP_066756921.1\|3621595_3622798_-	aminopeptidase	NA	NA	NA	NA
WP_066756925.1\|3623035_3623551_+	RNA polymerase sigma factor	NA	NA	NA	NA
WP_066756927.1\|3623563_3624664_+	TonB-dependent receptor plug domain-containing protein	NA	NA	NA	NA
WP_066756930.1\|3624763_3627541_+	hypothetical protein	NA	NA	NA	NA
WP_066756933.1\|3627544_3632074_+	TonB-dependent receptor plug domain-containing protein	NA	NA	NA	NA
WP_066756936.1\|3632414_3634385_+	VWA domain-containing protein	NA	NA	NA	NA
WP_066756939.1\|3634501_3635005_+	transcriptional regulator	NA	NA	NA	NA
WP_157886046.1\|3635075_3635420_+	hypothetical protein	NA	NA	NA	NA
WP_066756944.1\|3635427_3635829_+	hypothetical protein	NA	NA	NA	NA
WP_066756946.1\|3635907_3636327_+	hypothetical protein	NA	NA	NA	NA
WP_066756949.1\|3636338_3636716_+	hypothetical protein	NA	NA	NA	NA
WP_066756952.1\|3636712_3637525_+	DUF393 domain-containing protein	NA	NA	NA	NA
WP_066756959.1\|3637605_3638076_+	SRPBCC family protein	NA	NA	NA	NA
WP_066756962.1\|3638140_3638845_+	DUF2071 domain-containing protein	NA	NA	NA	NA
WP_066756966.1\|3638950_3639844_+	TIGR01777 family protein	NA	NA	NA	NA
WP_066756974.1\|3640062_3641505_+	alpha-L-fucosidase	NA	NA	NA	NA
WP_066756977.1\|3641771_3644435_+	glycoside hydrolase family 3 C-terminal domain-containing protein	NA	NA	NA	NA
WP_066756980.1\|3644756_3645179_+	hypothetical protein	NA	NA	NA	NA
WP_066759778.1\|3645259_3645520_+	hypothetical protein	NA	NA	NA	NA
WP_066756982.1\|3645750_3647139_+	dihydrolipoyl dehydrogenase	NA	NA	NA	NA
WP_066756985.1\|3647223_3647823_+	hypothetical protein	NA	NA	NA	NA
WP_066756987.1\|3647977_3648781_+	patatin-like phospholipase family protein	A0A1V0SKV5	Klosneuvirus	4.3e-12	32.0
WP_066756989.1\|3649084_3651028_+	band 7 protein	A0A2I7RWB7	Vibrio_phage	5.2e-27	26.3
WP_066756992.1\|3651079_3651517_-	hypothetical protein	NA	NA	NA	NA
WP_066756995.1\|3651666_3652398_-	ATP-binding cassette domain-containing protein	A0A2H4PQG7	Staphylococcus_phage	1.3e-34	35.4
WP_066756998.1\|3652481_3653075_-	hypothetical protein	NA	NA	NA	NA
WP_162271029.1\|3654136_3656656_+	T9SS type A sorting domain-containing protein	NA	NA	NA	NA
WP_066757004.1\|3656804_3657152_-	hypothetical protein	NA	NA	NA	NA
WP_066757007.1\|3657218_3657620_-	hypothetical protein	NA	NA	NA	NA
WP_066757010.1\|3657718_3658345_-	hypothetical protein	NA	NA	NA	NA
WP_066757013.1\|3658482_3658791_-	hypothetical protein	NA	NA	NA	NA
WP_066757015.1\|3659288_3659915_-	hypothetical protein	NA	NA	NA	NA
WP_066757018.1\|3659922_3663498_-	peptidoglycan-binding protein	NA	NA	NA	NA
WP_066757021.1\|3663540_3665007_-	ATP-binding protein	A0A109WUE1	Acidianus_tailed_spindle_virus	1.0e-11	32.8
WP_066757024.1\|3665091_3666534_-	hypothetical protein	NA	NA	NA	NA
WP_066757027.1\|3666585_3666900_-	hypothetical protein	NA	NA	NA	NA
WP_066757031.1\|3667574_3668138_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_066757033.1\|3668189_3669947_+\|tail	phage tail sheath family protein	NA	NA	NA	NA
WP_157886122.1\|3670935_3671742_+	hypothetical protein	NA	NA	NA	NA
WP_066757038.1\|3671781_3672213_+\|tail	phage tail protein	A0A059XP41	uncultured_phage	2.2e-26	49.2
WP_066757041.1\|3672238_3673579_+\|tail	phage tail sheath family protein	NA	NA	NA	NA
WP_066757038.1\|3673618_3674050_+\|tail	phage tail protein	A0A059XP41	uncultured_phage	2.2e-26	49.2
WP_066757044.1\|3674052_3674520_+\|tail	phage tail protein	NA	NA	NA	NA
WP_169816839.1\|3674723_3674885_+	hypothetical protein	NA	NA	NA	NA
WP_066757047.1\|3674884_3675604_+	hypothetical protein	NA	NA	NA	NA
WP_066757049.1\|3675605_3677351_+	type VI secretion system tip protein VgrG	NA	NA	NA	NA
WP_066757051.1\|3677353_3677644_+	PAAR domain-containing protein	NA	NA	NA	NA
WP_066757053.1\|3677790_3678201_+	GPW/gp25 family protein	A0A0E3FJY3	Synechococcus_phage	9.9e-05	32.6
WP_066757055.1\|3678289_3681343_+\|plate	baseplate J/gp47 family protein	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP015199

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection