CRISPRimmunity

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Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP014150	Paeniclostridium sordellii strain AM370 chromosome, complete genome	5 crisprs	WYL,DinG,DEDDh,csa3,cas3,cas2,csx1	0	3	6	0
NZ_CP014149	Paeniclostridium sordellii strain AM370 plasmid pRSJ16_1, complete sequence	0 crisprs	NA	0	0	2	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP014150_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP014150_1

629621-629730

Orphan

Consensus_repeat	Method
AAAACTTGTCCAACATGTAATGGAGAAGGAGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP014150_1

>merge|NZ_CP014150|1|629621-629730|CRISPRCasFinder
AAAACTTGTCCAACATGTAATGGAGAAGGAGAAATTAGAACGGCTCAAAGAACTCCATTTGGGAACATAATGAGTTCAAAAACTTGTCCAACATGTAATGGAGAGGGAGA

>NZ_CP014150|1|1|629621-629730|CRISPRCasFinder
AAAACTTGTCCAACATGTAATGGAGAAGGAGA	AATTAGAACGGCTCAAAGAACTCCATTTGGGAACATAATGAGTTCA
AAAACTTGTCCAACATGTAATGGAGAGGGAGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014150.1\|WP_057543653.1\|618819_619785_+\|stage-II-sporulation-protein-P	unknown	unknown	gnl\|CDD\|377838
NZ_CP014150.1\|WP_101508195.1\|631862_632330_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_158645311.1\|630479_631541_+\|dicarboxylate/amino-acid:cation-symporter	unknown	unknown	gnl\|CDD\|366058
NZ_CP014150.1\|WP_021129036.1\|625487_626510_+\|heat-inducible-transcription-repressor-HrcA	unknown	unknown	gnl\|CDD\|234621
NZ_CP014150.1\|WP_101508193.1\|617850_618807_+\|GPR-endopeptidase	unknown	unknown	gnl\|CDD\|237076
NZ_CP014150.1\|WP_055329824.1\|639148_640063_+\|DUF2935-domain-containing-protein	unknown	unknown	gnl\|CDD\|378573
NZ_CP014150.1\|WP_021129040.1\|619794_620052_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_101508196.1\|632436_633144_+\|noncanonical-pyrimidine-nucleotidase,-YjjG-family	unknown	unknown	gnl\|CDD\|162788
NZ_CP014150.1\|WP_055341161.1\|633295_634582_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_021124926.1\|617309_617576_-\|30S-ribosomal-protein-S20	unknown	unknown	gnl\|CDD\|376586
NZ_CP014150.1\|WP_054631651.1\|631553_631748_+\|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl\|CDD\|366058
NZ_CP014150.1\|WP_054631650.1\|627167_629003_+\|molecular-chaperone-DnaK	unknown	unknown	gnl\|CDD\|234715
NZ_CP014150.1\|WP_057561322.1\|624255_625386_+\|oxygen-independent-coproporphyrinogen-III-oxidase	unknown	unknown	gnl\|CDD\|180263
NZ_CP014150.1\|WP_021129035.1\|626525_627080_+\|nucleotide-exchange-factor-GrpE	unknown	unknown	gnl\|CDD\|271355
NZ_CP014150.1\|WP_057546651.1\|636561_637668_+\|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl\|CDD\|349932
NZ_CP014150.1\|WP_101508194.1\|622600_623929_+\|amino-acid-permease	unknown	unknown	gnl\|CDD\|273332
NZ_CP014150.1\|WP_021129039.1\|620186_621992_+\|elongation-factor-4	unknown	unknown	gnl\|CDD\|235462
NZ_CP014150.1\|WP_038293759.1\|635057_635768_+\|DUF5058-family-protein	unknown	unknown	gnl\|CDD\|379849
NZ_CP014150.1\|WP_054631655.1\|635781_636498_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_101508197.1\|637683_639018_+\|amidohydrolase	unknown	unknown	gnl\|CDD\|349947

Protein	Function_ID	Function_description	E-value
NZ_CP014150.1\|WP_057543653.1\|618819_619785_+\|stage-II-sporulation-protein-P	gnl\|CDD\|377838	pfam07454, SpoIIP, Stage II sporulation protein P (SpoIIP). This family contains the bacterial stage II sporulation protein P (SpoIIP) (approximately 350 residues long). It has been shown that a block in polar cytokinesis in Bacillus subtilis is mediated partly by transcription of spoIID, spoIIM and spoIIP. This inhibition of polar division is involved in the locking in of asymmetry after the formation of a polar septum during sporulation. Engulfment in Bacillus subtilis is mediated by two complementary systems: the first includes the proteins SpoIID, SpoIIM and SpoIIP (DMP) which carry out the engulfment, and the second includes the SpoIIQ-SpoIIIAGH (Q-AH) zipper, that recruits other proteins to the septum in a second-phase of the engulfment. The course of events follows as the incorporation firstly of SpoIIB into the septum during division to serve directly or indirectly as a landmark for localising SpoIIM and then SpoIIP and SpoIID to the septum. SpoIIP and SpoIID interact together to form part of the DMP complex. SpoIIP itself has been identified as an autolysin with peptidoglycan hydrolase activity.	1.77745e-71
NZ_CP014150.1\|WP_158645311.1\|630479_631541_+\|dicarboxylate/amino-acid:cation-symporter	gnl\|CDD\|366058	pfam00375, SDF, Sodium:dicarboxylate symporter family.	6.1632e-64
NZ_CP014150.1\|WP_021129036.1\|625487_626510_+\|heat-inducible-transcription-repressor-HrcA	gnl\|CDD\|234621	PRK00082, hrcA, heat-inducible transcription repressor; Provisional.	1.24453e-106
NZ_CP014150.1\|WP_101508193.1\|617850_618807_+\|GPR-endopeptidase	gnl\|CDD\|237076	PRK12362, PRK12362, germination protease; Provisional.	8.24362e-168
NZ_CP014150.1\|WP_055329824.1\|639148_640063_+\|DUF2935-domain-containing-protein	gnl\|CDD\|378573	pfam11155, DUF2935, Domain of unknown function (DUF2935). This family of proteins with unknown function appears to be restricted to Firmicutes. The structure of this protein has been solved and each domain is composed of four alpha helices. A metal cluster composed of iron and magnesium lies between the two domains.	2.01452e-36
NZ_CP014150.1\|WP_054631650.1\|627167_629003_+\|molecular-chaperone-DnaK	gnl\|CDD\|234715	PRK00290, dnaK, molecular chaperone DnaK; Provisional.	0
NZ_CP014150.1\|WP_101508196.1\|632436_633144_+\|noncanonical-pyrimidine-nucleotidase,-YjjG-family	gnl\|CDD\|162788	TIGR02254, hydrolase_haloacid_dehalogenase-like_family, noncanonical pyrimidine nucleotidase, YjjG family. This HAD superfamily includes including YjjG from E. coli and YfnB from B. subtilis. YjjG has been shown to act as a house-cleaning enzyme, cleaving nucleotides with non-canonical nucleotide bases. This family is a member of the haloacid dehalogenase (HAD) superfamily of hydrolases which are characterized by three conserved sequence motifs. By virtue of an alpha helical domain in-between the first and second conserved motif, this family is a member of subfamily IA (TIGR01549).	3.24586e-65
NZ_CP014150.1\|WP_021124926.1\|617309_617576_-\|30S-ribosomal-protein-S20	gnl\|CDD\|376586	pfam01649, Ribosomal_S20p, Ribosomal protein S20. Bacterial ribosomal protein S20 interacts with 16S rRNA.	7.33083e-22
NZ_CP014150.1\|WP_101508197.1\|637683_639018_+\|amidohydrolase	gnl\|CDD\|349947	cd09849, M20_Acy1L2-like, M20 Peptidase aminoacylase 1-like protein 2, amidohydrolase family. Peptidase M20 family, aminoacylase 1-like protein 2 (ACY1L2; amidohydrolase)-like subfamily. This group contains many uncharacterized proteins predicted as amidohydrolases, including gene products of abgA and abgB that catalyze the cleavage of p-aminobenzoyl-glutamate, a folate catabolite in Escherichia coli , to p-aminobenzoate and glutamate. p-Aminobenzoyl-glutamate utilization is catalyzed by the abg region gene product, AbgT. Aminoacylase 1 (ACY1) proteins are a class of zinc binding homodimeric enzymes involved in hydrolysis of N-acetylated proteins. N-terminal acetylation of proteins is a widespread and highly conserved process that is involved in the protection and stability of proteins. Several types of aminoacylases can be distinguished on the basis of substrate specificity. ACY1 breaks down cytosolic aliphatic N-acyl-alpha-amino acids (except L-aspartate), especially N-acetyl-methionine and acetyl-glutamate into L-amino acids and an acyl group. However, ACY1 can also catalyze the reverse reaction, the synthesis of acetylated amino acids. ACY1 may also play a role in xenobiotic bioactivation as well as the inter-organ processing of amino acid-conjugated xenobiotic derivatives (S-substituted-N-acetyl-L-cysteine).	2.54633e-165
NZ_CP014150.1\|WP_054631651.1\|631553_631748_+\|cation:dicarboxylase-symporter-family-transporter	gnl\|CDD\|366058	pfam00375, SDF, Sodium:dicarboxylate symporter family.	3.85832e-06
NZ_CP014150.1\|WP_057561322.1\|624255_625386_+\|oxygen-independent-coproporphyrinogen-III-oxidase	gnl\|CDD\|180263	PRK05799, PRK05799, oxygen-independent coproporphyrinogen III oxidase.	9.55401e-160
NZ_CP014150.1\|WP_021129035.1\|626525_627080_+\|nucleotide-exchange-factor-GrpE	gnl\|CDD\|271355	cd00446, GrpE, nucleotide exchange factor GrpE. GrpE is the adenine nucleotide exchange factor of DnaK (Hsp70)-type ATPases. In bacteria, the DnaK-DnaJ-GrpE (KJE) chaperone system functions at the fulcrum of protein homeostasis. GrpE participates actively in response to heat shock by preventing aggregation of stress-denatured proteins; unfolded proteins initially bind to DnaJ, the J-domain ATPase-activating protein (Hsp40 family), whereupon DnaK hydrolyzes its bound ATP, resulting in a stable complex. The GrpE dimer binds to the ATPase domain of Hsp70 catalyzing the dissociation of ADP, which enables rebinding of ATP, one step in the Hsp70 reaction cycle in protein folding. In eukaryotes, only the mitochondrial Hsp70, not the cytosolic form, is GrpE dependent. Over-expression of Hsp70 molecular chaperones is important in suppressing toxicity of aberrantly folded proteins that occur in Alzheimer's disease (AD), Parkinson's disease (PD), amyotrophic lateral sclerosis, as well as several polyQ-diseases such as Huntington's disease and ataxias.	1.53241e-54
NZ_CP014150.1\|WP_057546651.1\|636561_637668_+\|M20/M25/M40-family-metallo-hydrolase	gnl\|CDD\|349932	cd05683, M20_peptT_like, M20 Peptidase T like enzymes specifically cleave tripeptides. Peptidase M20 family, PeptT (tripeptide aminopeptidase; tripeptidase)-like subfamily. This group includes bacterial tripeptidases as well as predicted tripeptidases. Peptidase T acts only on tripeptide substrates, and is thus called a tripeptidase. It catalyzes the release of N-terminal amino acids with hydrophobic side chains from tripeptides with high specificity; dipeptides, tetrapeptides or tripeptides with the N-terminus blocked are not cleaved. Tripeptidases are known to function at the final stage of proteolysis in lactococcal bacteria and release amino acids from tripeptides produced during the digestion of milk proteins such as casein.	2.35834e-129
NZ_CP014150.1\|WP_101508194.1\|622600_623929_+\|amino-acid-permease	gnl\|CDD\|273332	TIGR00911, High-affinity_methionine_permease, L-type amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	3.3952e-67
NZ_CP014150.1\|WP_021129039.1\|620186_621992_+\|elongation-factor-4	gnl\|CDD\|235462	PRK05433, PRK05433, GTP-binding protein LepA; Provisional.	0
NZ_CP014150.1\|WP_038293759.1\|635057_635768_+\|DUF5058-family-protein	gnl\|CDD\|379849	pfam16481, DUF5058, Domain of unknown function (DUF5058). This family consists of uncharacterized proteins around 250 residues in length and is mainly found in various Firmicutes species. The function of this family is unknown.	7.68119e-74

>NZ_CP014150.1|WP_054631650.1|627167_629003_+|molecular-chaperone-DnaK
MGKIIGIDLGTTNSCVAVLEGGEPQIIPNSEGMRTTPSVVAFTKDGERIVGEPAKRQAVTNADRTIISIKTHMGTDYKVNIDGKEYSPQEISAIILQKLKADAESYLGQTVTEAVITVPAYFTDAQRQATKDAGRIAGLDVKRIINEPTAAALAYGMDKLDQEKKILVFDLGGGTFDVSVLEIGDGTFEVLATAGNNRLGGDDFDQVIIDYLAEEFKKTEGVDLRNDKMALQRLKEAAEKAKKELSSTMSTNINLPFITATAEGPKHLNIDLSRAKFDELTANLVEKTMEPTRRALQDAGLSTSDIDDVLLVGGSTRIPAVQEAVKKFIGKEPHKGINPDECVAAGAAIQGGVLAGDVKDLLLLDVTPLSLGIETMGNVMTKIIDRNTTIPTKKSQVFSTAADNQTAVDIHVLQGERSMSYDNTTLGRFQLTDIPPAPRGIPQIEVTFDIDANGIVHVTAKDLGTGKEQKVTITSGTNLSEEEIQQKVKEAEMNAEADKQKKDKIEAVNQTEATIYQMEKTLKEAGDKVDPGAKSEVEAEIVKLKELKDRENVTAEELNKAMEELNNKFHKIAEQMYQQTQQEQAQGGAQEEAKQDDNVVDADFREVDDQK
>NZ_CP014150.1|WP_021129035.1|626525_627080_+|nucleotide-exchange-factor-GrpE
MENNKQEELQEEVNENASEEVEETIEEAIEEATEAKDSSEADEKDKKVEELTDTLQRLQAEYANYRRRTQQEKETMGIFANEKILNELIPVMDNMERAMDACTDKEDSMYKGLDMVQKQLKATFEKFGLEEIDAEGQEFDPNLHLAVMQEPVEGIDANQVVMVLQKGYKLKTKVLRPAMVKVSC
>NZ_CP014150.1|WP_021129036.1|625487_626510_+|heat-inducible-transcription-repressor-HrcA
MTELNERKLNILKAIVKDYIDTAEAVGSRTLSKKYELGISAATIRNEMADLEEMGYLIQPHTSSGRIPSEKGYKLYVDSLMKEYELNTVEKHLIEESINKNMNYMNDLIHETSKLISKLTNYTTIAVTKNVSNLQNIKHIQLVGLDEKSIVLIIVTEKGEIKNTTISTNTYIDQAKLNLISDKLTRKLAGKNICEIDEEFLNYIKYEIAENSLIIDKLVESLNFGIEKNETSISLSGATNIFNFPEFSDVVRAKTFLTMLEEKDNISNMLKSKGIQKENLNIIIGSDNQCEVAQDCSIITATYNIDKDVVGKISLIGPTRMDYAKVYSILNYMGLLLNKK
>NZ_CP014150.1|WP_057561322.1|624255_625386_+|oxygen-independent-coproporphyrinogen-III-oxidase
MLGLYIHVPFCAQKCYYCDFNSYKIKSNEKEDYLINIEREMHLYKDEFKDKYFDTVFLGGGTPSILKAEELSRLFYKLHENFNIKKDAEITIECNPGTINKEKLKFMKKMGINRLSIGLQAVQNYHLKSIGRIHTYEEFERNYYDAIDVGFNNINIDLMYALPNQKEDEWRETLNKIISLNPSHISAYSLILEEGTKLYDMYENNEFKLLDEDTDIKMYEYTINTLKKYGYNQYEISNYAKTEKECKHNIIYWKCDNYLGLGPGASGYIDNKRYSNVENLKTYNGKLSKNLKPINEEIQLSEKDKIEEFIFMGLRMNEGINLDVFKERFNIEFLDLYKDILDKLIENKLLKLDGSNIMLTQKGREISNSVFIEFIN
>NZ_CP014150.1|WP_101508194.1|622600_623929_+|amino-acid-permease
MSNKGLQKTLGFSAALSTVVGMVIGGGVFFKPQAIYSATGGAPGLGMLAWVIAGVITIAAGLTAAEVSAAIPKTGGMMIYIKEIYGDRLGFLTGWMQAVLFFPATAAALGVIFAQQAATLIGQSEKNMAVVLPIAIGIILFLAILNTVGSKLGGTIQTVATICKLIPLALIIVFGFINGSGDNSITTPFIGENLSMGAVLGQVLIAALFAYDGWINVGSIAGEMKNPGKDLPKAIVGGLSIVMAVYVVINLAYLWVVPASEMATVSAPAALVAERIFGPIGGKIVTIGILISVFGGLNGYLLTGPRVTYALACEGTLPFSKGLSKLNKGGVPSNAIFLMAILACVYALSGQFNLLTDLTIFIIWVFYVLTFIGVMKLRKDQPKLERPYKVPLYPIIPLIAIAGGLFVIVNQLMNNTLIAAGGLIVTAIGLPVYSVMSKKNNN
>NZ_CP014150.1|WP_021129039.1|620186_621992_+|elongation-factor-4
MDNKQSRTRNFSIIAHIDHGKSTLADRLIQYTGLVSEREMKDQLLDNMDLERERGITIKLQNIRLVYKAKDGQEYFLNLIDTPGHVDFNYEVSRSLAACEGALLVVDAAQGVEAQTLANVYLALDQDLEILPVINKIDLPSARPDEIKAEIEDIIGLDASEAPLISAKSGLNIEDVLEDIVKNVPAPKGDTEAPLKALIFDSYYDAYKGVVAYVRVFEGTVKKGMTIKMMNTNKKFEVTEVGVMAPGQRELDELAAGDVGYIAASIKDIRSCCVGDTITDADNPTDEPMPGYKKATPMVYCGIYPGEGEKYENVRDALEKLQVNDAALEFEAESSAALGFGFRCGFLGLLHMEIIQERLEREFDLNIITTAPSVIYRVTKTDGEVVMVQNPANLPERDEIDIIEEPMVKGDIIVPKDYVGTVMELCQERRGDMINMEYIDEKRVMLHYDLPLNEVVYDFFDALKSRTRGYGSLDYELKGYVPSKLVKLDILINKEQVDALSFIVHESKAYSRGKSMCEKLKGEIPRHQFAVPIQAAVGNKVVARETISALRKDVLAKCYGGDISRKKKLLEKQKEGKKRMRQIGSVEVPQKAFMSVLKLDS
>NZ_CP014150.1|WP_021129040.1|619794_620052_+|hypothetical-protein
MSRIERKQEEKNKKRARRAVYRLLFLCMMICILSISTFLIDKEATLMIGEINTYNIEVFVKNIGKSIFESYKDIEEKLSKLNNLK
>NZ_CP014150.1|WP_057543653.1|618819_619785_+|stage-II-sporulation-protein-P
MISKKIISIGLITSVVFTICIKTSYALEDEKLLNFLINTSYPETKLEQPKDEENKEKEEENKKESKEDKKSSKKEDEFVKMYVGEENLPTEESSNEVAVTNGKYVDNVLVTKEQPNILIYHTHGGETYANSPAGNYHSDDKVNSTLEVGATLTKELSKRGRSVVHNTTYHDLPEFVGAYGRSLKTIETMQAKYSSIDMIIDLHRDGRKLDSKEAEKNFHDTCTANINGENVAKFMFVVGKKSENYAQNLKLAQEITAFAESKYPGITRPVVTKDNGRYNQFKSNKPLLIEVGGQMNTIEEAKASTKYIAEVLDEFFKQKGA
>NZ_CP014150.1|WP_101508193.1|617850_618807_+|GPR-endopeptidase
MISLRTDLALEAREIYEQGNDASNIPGVKIDTKELEDCIVTKVEVLDEQGAQIMNKGIGIYTTIESKLMKYDDDESREQVISYLKDELISILGNDKTKKTLVIGLGNWNITSDALGPKTVSKTLVTRHIFKNYNKDYDDDFTEVSGLSPGVMGITGIETSEIVKAIVEATNPDRVIAIDALASRKMERINSTIQISTAGISPGGGVGNKRKALNKEYLGVDVIAIGVPTVVDAATLTSDVLDLAIDNLMEQSKESEGFYNMLKQLKEDEKYHLIKDSLEPYDKNLIVTPKDIDDTIENLSIIISEGLNRSLHPGRTLN
>NZ_CP014150.1|WP_021124926.1|617309_617576_-|30S-ribosomal-protein-S20
MANIKSAKKRIKVIEKKTALNRARKSQIKTAIRKFEEAVTAGNREEAVARFQYAQKRISQVASKGTIHKNAAARKVAKLAQKLNGMNA
>NZ_CP014150.1|WP_158645311.1|630479_631541_+|dicarboxylate/amino-acid:cation-symporter
MRDFLKTYKSSFILLGCTILGAIVGLIWGPKATELKPIGDLFINLIMMIVVPLVFFSVASGVANVNSMQRFGKIMKNVVIVFTITTLVMAVVGILGSVILDPAKGIDIQSVKEMMVAPDQEKLASKGSLLTQIVNSVTVSNFGDLFSSSNLLQLVVFAVLVGSSVAVLGDKANTIRKILNEGTSVVLNVVGIIMKLGPIGLGCYTASIIGELGQEIIAGYIRVFGTYCLIAIIYFIVCYTLYAYVAGGKKGVKKFYENSISPIATALATSSSSACIPSNLEASKKIGVPDDIAETVIPLGINIHKDGSVLAVIVKVAFLTGIMGGNMANPETLINLLVTVMVVGVFMAPVAGG
>NZ_CP014150.1|WP_054631651.1|631553_631748_+|cation:dicarboxylase-symporter-family-transporter
MLVVSIFGFPVEAIPLLTVITTITDIPNTVLNTTGNTVSSMLVARLVEGKNWLKDEVTNLKKVG
>NZ_CP014150.1|WP_101508195.1|631862_632330_+|hypothetical-protein
MDKFNFIIDGNHITNEKDLHNFILEKIDSIDYVVEYDLRGKKKKKPDCKPPGPSPVCLKLMFPYKVEVMRGCKQMIFGILVDKHGHPIKHPIIEFELSDYSLGNLSFSPAISFGDGCFCTTFVGERVGRGFIKMCCRGTDLDRIVPVEVKENHCC
>NZ_CP014150.1|WP_101508196.1|632436_633144_+|noncanonical-pyrimidine-nucleotidase,-YjjG-family
MKQYKYLIFDLDDTLLDFQDNERNSLKVIFEKYNIPFEEKSINKYKAINRSFWSQIEQGTIKKEEALTKRFEEFFALYGYNVQGEVIEKEYQNCLNKGHKTIPKAMETLMDLRIRGYKIFAGTNGVGKTQNQRLKDSKLIDFFDDVFISEEMGVEKPNSKFFEIIFNKYDFMKKDETLMIGDSLASDIKGANNFGIDSMWFNSLNKECGEIKPTYEIHELSEVLEVLNKEAVAAV
>NZ_CP014150.1|WP_055341161.1|633295_634582_+|hypothetical-protein
MIIGVLGPLDSATRIEKILKDIDSGLETRLYTKEKIVESIDLIEACELECDGIILTGCGVYEEILKKYEIKKPHSFVQRSDTSILKAFWEIQSQGNLIDKFSIDVVEDDMVKNIIEEFNIEHKAMYCLPFSTDINEDEYLKWHTDLYLNKEVNIIITAFMNIYNQLKDQGYPIILLKPTRALVKVAYDEVINQFAINKAEFSQIAVEIFNFGNSSRNIENYYSNMIKKTDIDRYIVEYVRSINGAVFPFGRNEYIIFSNKGSVNKSKNYKKLIKLQKEIKSLGFDLNIGIGFGANAFKAEINASKALERGIDSGESYIYSIDEEENLTGPLGLDNEISYCIVPNDQSILDISSQTGLSCETISKIMGINEIRESKIYDSKELAGYLDISDRSARRILQKITTSGLGKVHAKESNKGAGRPKNLIEILF
>NZ_CP014150.1|WP_038293759.1|635057_635768_+|DUF5058-family-protein
MANHPFMWLAAGLAVTVVIVQSIVFFRKSVVAAKEMGIKDTQVKAAIKSSAISSIGPSIVILVGMISLLVSMGGPISWMRLSFIGSVNYELMAAGFGAEAMGAKLGAGMDPMVFACAIWVMVLGSLGWLIFTLLFTDKMDKVNHLLSSGNEKLVPIISACAMLGAFAYLASGNFITGEGSVTFTSPAAVATIIGCVVMMGLSKIAKDKNIQWIKEWALSISMFSGMIIGTVLINVI
>NZ_CP014150.1|WP_054631655.1|635781_636498_+|hypothetical-protein
MSNNNYYSKKYIPSITKWGKGTLLLGIVLCFAPLIVVSGIFGYMPPIAAIIAGTISQISVSGAFYIVEPIAYFPILGIPGTYMTFISGNTSNMRVPCAMVAQEAADVEPGTEKGSVISTIGIAVSIIVNIIILSVGVVFGQAILSVLPPQVTAAFDLILPALFGAVFGQFAIMKPKFAAVAALIAVPMNFLLKNGVFDFMPGSGSPSYLVILTAVFGTILIGKKINEKEEAKQNNRAA
>NZ_CP014150.1|WP_057546651.1|636561_637668_+|M20/M25/M40-family-metallo-hydrolase
MLSRERLVNNFIDMVKVDSPSNKEIEMSKWLVNYLTERGIEVKVDDAGEKFGGNSGNIIAYIKGEDSENPICFAAHMDQVAPCLGVKPVVKGNIIETDKTTTLGADDKAGIAAILEALECVMEDKIPHRDIYLLFTVCEEAGMLGAKNFNPENLPCKDVVILDAGGATGVIAYKAPAQENIKVTFYGKKAHAGIEPEKGINAIVAASNAISNMHIGRIDEMTTSNIGRIEGGGATNIVTDEVSFTAEIRSHIPNRLEEEINHMKICCEEAAKNMNTTCDFEHTNAYPSFELSLDSDVFKLVEEATKKVGIEPKPMVIGGGSDANIMANLGYQSAIISLGMYDVHTVNEYVNIDELYDATKIVYNIMAL
>NZ_CP014150.1|WP_101508197.1|637683_639018_+|amidohydrolase
MNKKELKRLVLEEIDKNKDKIIEAGRSIYKTPELGYKEVKSTKIASEFLKSLGVEVVDNIAVTGCMTSLNKDKNGPKIAVMGELDSVVCPDHKDANEIGNIHCCGHNIQVAGMLGCAVGIINSGVLKYLDGKIDFMAVPSEECIDLEFRKSLQEKNEIKYVGGKQELLYRGTLDDVDMAMMFHALNFEENKNCVIKSYTNGFVSKHATFIGRASHAGIAPHEGINALNMASLATNNINAQRETFKDEDRVRISTVINHGGDIVNVVPSKVTIEAMVRAATVDAMIDANEKVNRSLHAAAMALGGEVIIEDTIGYLPLDSDDSMDFIFKKNYVELVGGSEESIVDVIKTAGSTDFGDISQIIPCIHPWIGGVSGSLHTKDYYISDEELAYIIPAKAMAMTIIDLLVDDAKIAKDIVEKFKPIFTKESYLDFMDKNTNTYKYDYKK
>NZ_CP014150.1|WP_055329824.1|639148_640063_+|DUF2935-domain-containing-protein
MINDQRYVILSLELHLFFARIMKEHSLFLESGFVTKDSKLELEADHYKREFEKLLGYAISASNGVIRDDILKSGEIVTDYTLGTEQKTQNLTGIDINQNLTVLESKLRSGNDPKVSENLINYVNQLNNNSKLLLNGLISFKERLLNGVLSCNLFTSNYPLLIEHILREAKLYLSLVQDLEHRVDIETKSNKETELFWDQIMMEHSLFIRGLLDPSENKLIETADEFADDFEDLIKEARNMTDATINSMTDETLEKTIELKNFKQAGTEGIASCKIRSIILPLLADHVLREANHYIRILESYKRK

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Crispr_ID: NZ_CP014150_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP014150_2

1152406-1152480

Orphan

Consensus_repeat	Method
GTATCAGGGGTATTAAAAAATAGT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP014150_2

>merge|NZ_CP014150|2|1152406-1152480|CRISPRCasFinder
GTATCAGGGGTATTAAAAAATAGTAAAAACATACAGTGTGAAGAATTTAAAGTATCAGGGGTATTAAAAAGTAGT

>NZ_CP014150|2|2|1152406-1152480|CRISPRCasFinder
GTATCAGGGGTATTAAAAAATAGT	AAAAACATACAGTGTGAAGAATTTAAA
GTATCAGGGGTATTAAAAAGTAGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014150.1\|WP_055329278.1\|1160733_1161192_-\|ImmA/IrrE-family-metallo-endopeptidase	unknown	unknown	gnl\|CDD\|368753
NZ_CP014150.1\|WP_158645323.1\|1149779_1150208_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP014150.1\|WP_021128552.1\|1156923_1157190_+\|mor-transcription-activator-family-protein	unknown	unknown	gnl\|CDD\|337191
NZ_CP014150.1\|WP_057543393.1\|1141835_1142591_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224059
NZ_CP014150.1\|WP_021128555.1\|1153791_1154412_+\|DUF4004-family-protein	unknown	unknown	gnl\|CDD\|379048
NZ_CP014150.1\|WP_101508411.1\|1152966_1153782_+\|polymer-forming-cytoskeletal-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_101508404.1\|1142577_1144677_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|376899
NZ_CP014150.1\|WP_101508413.1\|1161779_1161998_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|224393
NZ_CP014150.1\|WP_101508409.1\|1150434_1152123_+\|FUSC-family-protein	unknown	unknown	gnl\|CDD\|379231
NZ_CP014150.1\|WP_021128554.1\|1154462_1155257_-\|YitT-family-protein	unknown	unknown	gnl\|CDD\|224203
NZ_CP014150.1\|WP_101508403.1\|1140996_1141698_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|225818
NZ_CP014150.1\|WP_101508407.1\|1147476_1149714_+\|FtsX-like-permease-family-protein	unknown	unknown	gnl\|CDD\|226957
NZ_CP014150.1\|WP_055329280.1\|1156111_1156630_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_021128549.1\|1161210_1161612_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP014150.1\|WP_021123572.1\|1155596_1155971_+\|CGGC-domain-containing-protein	unknown	unknown	gnl\|CDD\|378059
NZ_CP014150.1\|WP_101508412.1\|1157618_1160696_+\|collagenase	unknown	unknown	gnl\|CDD\|366791
NZ_CP014150.1\|WP_101508405.1\|1144801_1146019_+\|FAD-binding-oxidoreductase	unknown	unknown	gnl\|CDD\|223737
NZ_CP014150.1\|WP_101508402.1\|1139716_1140988_-\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|340412
NZ_CP014150.1\|WP_057579392.1\|1146778_1147477_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213222
NZ_CP014150.1\|WP_057540381.1\|1146152_1146779_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228

Protein	Function_ID	Function_description	E-value
NZ_CP014150.1\|WP_055329278.1\|1160733_1161192_-\|ImmA/IrrE-family-metallo-endopeptidase	gnl\|CDD\|368753	pfam06114, Peptidase_M78, IrrE N-terminal-like domain. This entry includes the catalytic domain of the protein ImmA, which is a metallopeptidase containing an HEXXH zinc-binding motif from peptidase family M78. ImmA is encoded on a conjugative transposon. Conjugating bacteria are able to transfer conjugative transposons that can, for example, confer resistance to antibiotics. The transposon is integrated into the chromosome, but during conjugation excises itself and then moves to the recipient bacterium and re-integrate into its chromosome. Typically a conjugative tranposon encodes only the proteins required for this activity and the proteins that regulate it. During exponential growth, the ICEBs1 transposon of Bacillus subtilis is inactivated by the immunity repressor protein ImmR, which is encoded by the transposon and represses the genes for excision and transfer. Cleavage of ImmR relaxes repression and allows transfer of the transposon. ImmA has been shown to be essential for the cleavage of ImmR. This domain is also found in in metalloprotease IrrE, a central regulator of DNA damage repair in Deinococcaceae, HTH-type transcriptional regulators RamB and PrpC.	1.75074e-17
NZ_CP014150.1\|WP_158645323.1\|1149779_1150208_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	8.28916e-13
NZ_CP014150.1\|WP_057543393.1\|1141835_1142591_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224059	COG1136, SalX, ABC-type antimicrobial peptide transport system, ATPase component [Defense mechanisms].	9.75965e-102
NZ_CP014150.1\|WP_021128555.1\|1153791_1154412_+\|DUF4004-family-protein	gnl\|CDD\|379048	pfam13171, DUF4004, Protein of unknown function (DUF4004). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are approximately 210 amino acids in length.	1.79564e-77
NZ_CP014150.1\|WP_021128552.1\|1156923_1157190_+\|mor-transcription-activator-family-protein	gnl\|CDD\|337191	pfam08765, Mor, Mor transcription activator family. Mor (Middle operon regulator) is a sequence specific DNA binding protein. It mediates transcription activation through its interactions with the C-terminal domains of the alpha and sigma subunits of bacterial RNA polymerase. The N terminal region of Mor is the dimerization region, and the C terminal contains a helix-turn-helix motif which binds DNA.	8.04073e-13
NZ_CP014150.1\|WP_101508404.1\|1142577_1144677_+\|ABC-transporter-permease	gnl\|CDD\|376899	pfam02687, FtsX, FtsX-like permease family. This is a family of predicted permeases and hypothetical transmembrane proteins. Buchnera aphidicola LolC has been shown to transport lipids targeted to the outer membrane across the inner membrane. Both LolC and Streptococcus cristatus TptD have been shown to require ATP. This region contains three transmembrane helices.	0.000130554
NZ_CP014150.1\|WP_101508413.1\|1161779_1161998_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|224393	COG1476, COG1476, Predicted transcriptional regulators [Transcription].	2.56914e-13
NZ_CP014150.1\|WP_101508409.1\|1150434_1152123_+\|FUSC-family-protein	gnl\|CDD\|379231	pfam13515, FUSC_2, Fusaric acid resistance protein-like.	1.14547e-17
NZ_CP014150.1\|WP_021128554.1\|1154462_1155257_-\|YitT-family-protein	gnl\|CDD\|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	1.08564e-65
NZ_CP014150.1\|WP_101508403.1\|1140996_1141698_-\|response-regulator-transcription-factor	gnl\|CDD\|225818	COG3279, LytT, Response regulator of the LytR/AlgR family [Transcription / Signal transduction mechanisms].	3.8886e-39
NZ_CP014150.1\|WP_101508407.1\|1147476_1149714_+\|FtsX-like-permease-family-protein	gnl\|CDD\|226957	COG4591, LolE, ABC-type transport system, involved in lipoprotein release, permease component [Cell envelope biogenesis, outer membrane].	3.38771e-12
NZ_CP014150.1\|WP_021128549.1\|1161210_1161612_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	2.71669e-15
NZ_CP014150.1\|WP_021123572.1\|1155596_1155971_+\|CGGC-domain-containing-protein	gnl\|CDD\|378059	pfam08821, CGGC, CGGC domain. This putative domain contains a quite highly conserved sequence of CGGC in its central region. The domain has many conserved cysteines and histidines suggestive of a zinc binding function.	1.38897e-24
NZ_CP014150.1\|WP_101508412.1\|1157618_1160696_+\|collagenase	gnl\|CDD\|366791	pfam01752, Peptidase_M9, Collagenase. This family of enzymes break down collagens.	2.28185e-69
NZ_CP014150.1\|WP_101508405.1\|1144801_1146019_+\|FAD-binding-oxidoreductase	gnl\|CDD\|223737	COG0665, DadA, Glycine/D-amino acid oxidases (deaminating) [Amino acid transport and metabolism].	4.95671e-48
NZ_CP014150.1\|WP_101508402.1\|1139716_1140988_-\|sensor-histidine-kinase	gnl\|CDD\|340412	cd16935, HATPase_AgrC-ComD-like, Histidine kinase-like ATPase domain of two-component sensor histidine kinases similar to Staphylococcus aureus AgrC and Streptococcus pneumoniae ComD which are involved in quorum sensing. This family includes the histidine kinase-like ATPase (HATPase) domains of various two-component sensor histidine kinase (HKs) including Staphylococcus aureus AgrC which is an HK of the accessory gene regulator (agr) quorum sensing two-component regulatory system (TCS) AgrC-AgrA. The agr system plays a part in the transition from persistent to virulent phenotype. This family also includes Streptococcus pneumoniae ComD HK of the ComD-ComE TCS, involved in quorum sensing and genetic competence.	9.54418e-35
NZ_CP014150.1\|WP_057579392.1\|1146778_1147477_+\|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.	6.00423e-94
NZ_CP014150.1\|WP_057540381.1\|1146152_1146779_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.59265e-17

>NZ_CP014150.1|WP_101508409.1|1150434_1152123_+|FUSC-family-protein
MILIQIFYITIFGRHNIIIGIILGLAAVGFINRDFTGQILYRTITFLIINLYLAIAAYFATTNIYIGLIINFITIFMVTYVYMNDYKHPTSYTFLMAYIFMVCMKINIDELPLRLLAVSMGVIFIILPQIILNRKQFEKKSTNIIKNIVKEILEQIDDLIDGKYEEGKSIKINQKIRSLVICINERINNSFKKNKHKVNMFNIAICLSRLNIIINHISKCKMDKDKRDEYLNDLKLQIINIDKFNDGLNSFEIINKNIDDFANRYKKLGKKINLVDESIYVLKIFLKRISVNEESDNTISSKVYKTVNMPKRFNMVESMKENFNIKSLRCRYSIKLAMAISILIFLGNIINIEHKAWVIISAYIVLQPYQEDGVVKAKKRFIGVTKGVLIFFITFSLIKDYVPIIVILLFTFTGYFYFTDYSKKVIMTTILSLSSISLVENIDKTSLSRFAFVSIGIGIGLLFNKYFLPYQIEDSIKELKHKYKKNTKAILKEIHLIMEEKHDTGKLMSLSMERNKIENKLILNYNKLNKKDLEKFVYEENMKMSDEKYTLLKHFYKNSNIK
>NZ_CP014150.1|WP_158645323.1|1149779_1150208_-|MarR-family-transcriptional-regulator
MEIIDTLNLIRSTSLLRKNYANFVNKSLSNSDITLSEFAYLKEVVNCDGIAQDELIRNLSIDKAAATRIAQSLEKKEIIKRVRNENNKRFFNVFLTDKGHKYADFIKQTLSDFYNVLNNEVSSSDMKTFMTIFKKINGSFEE
>NZ_CP014150.1|WP_101508407.1|1147476_1149714_+|FtsX-like-permease-family-protein
MKLNKSIIRVMKENMGKYLGMLYMLILSVFLFVSLNLTAQNLRYNKDEYVTKNVQEDLEFYTLNKIDDISKIEDKFDLKMDETLVKDYKYNGKTLRLFTPNDKVNITAVLEGSMPKVGEIALDPQFAKANKLSIGDNYKIGDSSYKISGFIGIPNYAYILEKEGDIINNPKKFGIGILNEEDIKGATYLYSVKYNDKNKNIYNSSKDLKSHLSEEKVVVTDWIYAKNNLKISVLDIEVMAISTYSIILPTIILLITVVLISIVLGRMIKNDMAGIGTLYALGYRKKEIMMHYLNYPIILSLTGGLVGGVIGLIVQKYIFDLFLTFFPIPVEKLSYSPMYFILGIVLCVLFTVVGSYISINKILKASPVSLMKNEFKTKKVNIIERKINLKGFKFKTKFAIREQLRSIPRLAFLVIGVSIATIFLMYGFIAKCSMDYAINQDNNNIFSYNYEYILKQPTTDKAPKGSKAISGTRFAIDTTLKDKFELLGVSKNSDMVILKNKDGSKISIDDDKFIITSKMAKEYKLDVGDKLSFINMMDDKKYSLTITDIAKSNTGDYVFTSLDNFNKMMGLKKGEHSAIISKSPIKIDKDLLYMTNTPSNMKDMLADYMDLMETFIYAIAVVAFIIGIIIVYIIASISIDENKNNIALMKVFGYKKKEINSMMLNGSRIYVVIGYIIGVPIGYFIIDLIFKIFAELDIGLEAKITLPYILIGFVIIALTFEISKAICSRKIEKIALSEALKTQKE
>NZ_CP014150.1|WP_057579392.1|1146778_1147477_+|ABC-transporter-ATP-binding-protein
MFIKTSNLCKSYKTEDVETIALNKVNISLDKGDIGVILGPSGSGKSTLMNILGGLDRADTGQAIVDGVDILKLSDDELVEYRREKTGFIFQSYNLMPHLTVLENIEIIENISKSPLDINEVLQAVGLINKANRFPKELSGGEQQRVAIARAVIKNPAILFCDELTGALDYNSAIDVLSLIQDINRTFNTTILIITHNASISAMANKVYKFRSGEVSDFIINNNPVDAREVKW
>NZ_CP014150.1|WP_057540381.1|1146152_1146779_+|TetR/AcrR-family-transcriptional-regulator
MNKTFENLSEEKQLRIINSAIEEFANKGYKRATVDNIVSKAGISKGSIFQYFKNKERLYLYICDYQIKIITDEVFKQKENNENDFFKLYKQASRVKFEILKKNPYIFKFFKTLYSDDSQVAQKWLENILKNKDQLVLNFIGDYDKSKFRDDIDIDMAIKTIELTFDGLSMKWMDKLSYENYESDLKSLFEEVENYINFYKKLYYKGEN
>NZ_CP014150.1|WP_101508405.1|1144801_1146019_+|FAD-binding-oxidoreductase
MKIQYVQGKPLFTTINKNKKQYPYLTDDIETDICIIGGGVTGAIASYYFSKQNIKTVILEKKRIAHLSTSVTTSLLQYELDDNLSDLQEYTRLENSLKAYNLGLRALDEIEEFVNTYGNKCDYKKKDALLYTAKNSEVNSIKIEYDLRKENGFDVEYIDETTNEFSFDLKAGIIAKNGGAELDPYKYTNQLLEVALDNGLKIYENTEVVDLVHHEDYIDVITEFGYRVKAKKIIVATGYNTKLFTDRNFATKTTTFNVVTKPVSNFDGWKDRILIRDNCDPYNYLRTTDDNRIIIGGEDVSFIPDIFDEKLANKKYDILEARLKSMFKDIDNIEIDFKYCGTFASTPDNLGFVGPDHKHKNLWYLLGYGANGILFAILGAMMLTKLYEGREDENMKLFKVDRFDK
>NZ_CP014150.1|WP_101508404.1|1142577_1144677_+|ABC-transporter-permease
MTMNSVISKLRKNSIKNYYMLAFCITLSVLLVTSYALMLFSPTVMNILPSGGDSRKQGYMIFSIAIIGCSVFTTYASSLFFKYKSHEFGVLMALGERKSKLKKVLLNELLFIIPICLVVGLVLSVPVSYIIWKIFQIFIIDTKEMVYQFGATGLIFGIGFCVFVTICIFINGAKFIKRSNIMDVIYEQRKSEVVKDIKPWTGIVGWILVIGGLFLGYGVPTIVIELTGYNMPAIWDVVYLLSFVGLYMVLTYAIIYSKKGKNPKKYYKNIISTNMMRFSGKQTVRNMCVITFLIAGGLFASFYGPTMIANLLIDIKNNPIDYAFYYKGNENQIKKGEIYSLAKDNNVDITEYYEVDSISLITNGYYRDYDENNMIITEYIKKMQYNEFFKESDFNKVSGQNIDVNKGEYYKVIANGESEMIWSKFNDLDTITHPVTEKSEKIKFKGTVSFRPFVKENQGKYVISDEDYERLSKGLPKEQYDKFVLFNVINPSETYKFAKALKEEIINRSSKDAAVSISFDEYEKMLAQKKGEDYTYDFKLELSPDDNQLFDEWKYYPMFKPLDQQDLLKNMAVFIMLFTYIAIICLASTAIITYTRAITIGLDNKQLFSDIKKLGANKKYIEKNIKKQLAKIFIYPTVIGSIFTYMIYITMFFGNSRGNISQGEFLGLVVGLVIILLVIIYMFIIYKFSLKKVKRIAKI
>NZ_CP014150.1|WP_057543393.1|1141835_1142591_+|ABC-transporter-ATP-binding-protein
MLKVNNLYKSYKTGNMNYDVLKNISFYVKKGEFVAVMGPSGSGKTTLLNCISCFVPFEKGEILLGGENISGLNEESLADIRNQKLGFVFQDFMLLDGLSVVENICLPQIIADKDVTKMEVLANKLCNTFGISHIKDKYPAEISGGEKQRSAVARALINKPYIILADEPTGNLDSKSCRAVIDSFVQAKKELGATVFMVTHDSFAASFCDRVIVLKDGEVYTELTKTTSRIEFMDKLLDTLKKLGGDDCDNE
>NZ_CP014150.1|WP_101508403.1|1140996_1141698_-|response-regulator-transcription-factor
MLKIAICDDEKYQINLLKNILSIHLDLKGLDYRIYEFDCGESLIDSITKESYDIIFSDIEMKALNGIDTAKNIRLHNKKSVIIFVTSYPDFVFQGYEVKAFNYILKPYTSEKIGKVLDSALEELNEIQDKFYVVESKSKTVKINLSNTYYFTSDKRKVNAVTFTETIDFYDKLDNLEKNLPSFFVRIHQRYLVNINHVSSVKSCSLVINKEVLPISRGRYNSFMIEFAKTMLR
>NZ_CP014150.1|WP_101508402.1|1139716_1140988_-|sensor-histidine-kinase
MYNIIYNLTTVILYIVISYYFYKVIANFSSVKDNKYAKFASIFGAYLVPNVIIYTSDIVNIFYTMIGFILIMVVFYKSSYIKNISAVMIFYPIVVSINLMANDFCTKIYFYLGKTLWMDYFAHTLEMCIISLSWFLIYHFSKDKLSNIDRYIDIKTWVMIDIICLAPFISIISTNINTPMGKEYQAYPIAIACIVTSLSMIFLIEYIVKSVKNRLENQNLKLEYSYYRELEENQKNVRKLNHDMNNHLSVIYSFLEYDNLEGAKEYFNELSDKFNVTNRVFCKNSIVNAVINSKYNLAIKNQIDCFFNIDIDEILPLEDIDLCSIFSNTLDNAIEASLKLDDISKRKISLKARCDKGYFSFSICNNYNGIIKFNKGKYSSTKSDSSMHGFGLENVSEIVNKYSGTLDINYSKFEFNILAIIKI
>NZ_CP014150.1|WP_101508411.1|1152966_1153782_+|polymer-forming-cytoskeletal-protein
MEKSNIKLIGDGFISEGEYNNIKIIGDGTSEGNIVANKVKILGDCNFDGILDFESLKVTGDFETKGVLKCKDFKVVGSARIDGDLICDSIKVMGDLVVKGTCKINDLVVTGEMESFYNMECNNVTIKGYLSCKESINSKYIKSYGDLNVGKNIESETITIYGKIICDGLLNAEEVIIVPRGRCKCSEIGASNIEVTKKPKGIFKPITLFDKMGVLSCNLIEGDSIYLERSNVENIRGREIKLINKCNIGNVEYNDLLEVSSDSTVVSSSRV
>NZ_CP014150.1|WP_021128555.1|1153791_1154412_+|DUF4004-family-protein
MEENLISKKELLEVTNISYGQLYRWKRKKIIPEEWFIKKSSFTGQETYLPKDKILERIEYILSMKDEISLDDMANMFAKSDSDKKFDIDIIMAKNAICESTKNIFEQITNAKYIGKKEILILSIIEKYLIKSIITLEELKQVVSVINNGFDVLYNEESKIFLFRKLGIPFVVGCKSYKDVFFEEDMVKILEIDVIREISEMGRKII
>NZ_CP014150.1|WP_021128554.1|1154462_1155257_-|YitT-family-protein
MSVGLNMFLEPYMIASGGLTGLAIVLKNLFNTPLWFINLVFNIPLFIFGIKILGKRDAIKTLIGILFLTFFLKVTEPLTSAFQTNDVLLSSIAGGIVVGISLGMLFRIDASTGGTELACLILNKIFPFISISVFMFIIDGLVIALAGLVSRNIQIALYAIVSLYISVKICDTIVEGFDFSKSFIIVTDHSDEISDSIMENLERGVTFLEGRGGYSKQRKDVILVVVSRREEVVLRKLVNEIDPLAFVIINNAYEVLGEGFTRKV
>NZ_CP014150.1|WP_021123572.1|1155596_1155971_+|CGGC-domain-containing-protein
MKKVAIYVCGEVSRKCTANGCLRTFNAMEDSFERYKEDGCKLVAFNTCNGCDQDPVESLDVKIEKLKKADVEVMHISTCIRGRCSHYEEYAKEFAKHFEVIGYTHGSKEGKKNNNINYIKDIEK
>NZ_CP014150.1|WP_055329280.1|1156111_1156630_+|hypothetical-protein
MKKIGIIITLILLVISLVGCENSESKKAVEQGKVEMNNKEYDKALASFKVALDKDSGNEEAKRLTTLINNYNKANVEFEKDNIDDANKFMNQIDEGTIEDSIKNDIDNLKAKIHEQEKIDKEIVHIKELIKDKKYEESKKSIDKIDSDKLTNKDKKEIDELKDEIYLGLLQI
>NZ_CP014150.1|WP_021128552.1|1156923_1157190_+|mor-transcription-activator-family-protein
MLEKLKIEDLPDSYKDVAEEIGIDSFKKLVKLLGGNSLYIPKEVSLTRPIRDRIIKEDFNGDYKILSRRYNISQSQIRNILDKQTKGV
>NZ_CP014150.1|WP_101508412.1|1157618_1160696_+|collagenase
MKYKNHAKYIAGTLICSFGVTTIQSPILSHAMDSKNAKNINMFNNNDKEVRNTTNQNNKDKADRLTAEEASVHKKDKMIGKQSIDNVKKDKKSINYTMADLNKMSNEELIKTLEQINWYNITDLFEYNKDAQEFYGNREKFDFLIKTLEQKGTKYTSQNHEGIPTFVEVIRAGFYLGFYNEGLSYLYELETREKCLPAMISIQKNPNFKLGENGQNEVIKSLGMLIGNSAVSVDVVNNMIPVFEQYNQDLKNNMNNFGKSDIIYNIMKGVEYRLNAYAYDSKLQPEETQFAKKIDKYIDIVSDYMSNKPENDSEEWFIECGMYYTSKLYKFHSKPNQIHAKMDKVLEINEEMSWLYLKAVDLIEWYMGGTLSDGTPINSKEIKEKAKKYYLPNEYKFEDDKIVIKTGDKVTAEKVERLYWATKEVQSQFFKIIGSDKALEVGHADDILTVVIYNSPKEYKMNQVLYGYSTDNGGMYIEGEGTFYTYERTPQESIYSLEELFRHEYTHYLQSRYLIEGYFGTGDFYKDKDWRITWFEEGSAEFWAGATRTDNVISRKSMVSGISKNPSDRFTVDKLMHSKYGSWDFYNYGFAFVDFIYRERPEIFEKFTDLMITNNVAGYDKYVEELSKDVELNKGYQAYMQKLVDNYDNLTVPFVSDNYLKEHPSRDISKIKEDIDKTINLKNSKVETKKKATLNKYKVSGKRGKSSIESEKSPLFNTYTFSGIFEGGKSNGRTSDNKEMGEILNTTLKKLEQIGWSGYETVNAYHTDYKVNENGNYEFRIVFTGILPKGSQEVVNDDTFETANGPIKINTNYSGDLSDTDNKDYYYFNLYNPSNINITLENLDNKGVSWQLFHESDLNNYVAYPTTSGAVLNGDYNATKTGKYYILVYNHDKSIANYNLKVNFGNSNDDGVEQEDNNSFEKANPFNINQLIKGELDNSKDTSDYFKFEVKEDASLNISLEKTEGDGVNWLLFKDSDLENYIASPTESIDNKLNGKVDLKVGTYYLEVYGYGSSPVKYNFKVTPN
>NZ_CP014150.1|WP_055329278.1|1160733_1161192_-|ImmA/IrrE-family-metallo-endopeptidase
MGILDKIKDSIKGLVNKNKTRNPFELAEALGIILVEAPLKDGLNGCYHERSGFQFIYINSDLPYEKRLMVAAHELGHAILHRGRNILYLSNNTYYTRGTFEREANLFAAELLLEDDFFEKYKHIENCTLEYVSQCECVSYELVDYKLKYLSE
>NZ_CP014150.1|WP_021128549.1|1161210_1161612_-|helix-turn-helix-transcriptional-regulator
METLSTRLKELRKEKGYTLEQMAQDLNTTKVTLSRYENGTREPKSETLNQLSDYFNVSIDYLFGKTDERNPKTKDEIIDVKKAIEEIKDELENSNSLMFDGECLSEDAISSLLSAMEVGLSIAKKKQEEMKNK
>NZ_CP014150.1|WP_101508413.1|1161779_1161998_+|helix-turn-helix-domain-containing-protein
MIYKNNLKGIRVSRGLTQGDLAKLINMPRSTYIKKENEKSYFNIKEAMKIGKVLNLSIDYIFLTQSYQIGKK

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_CP014150_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP014150_3

1163912-1164027

Orphan

Consensus_repeat	Method
GCTTTAACGTTTCGTCAAATTGATATAACCACATCACTTAATAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP014150_3

>merge|NZ_CP014150|3|1163912-1164027|CRISPRCasFinder
GCTTTAACGTTTCGTCAAATTGATATAACCACATCACTTAATAGTTACTAAACTGCATTTGGGAAGTAGAAAGCTTTAACGTTTCGTCAAATTGATATAATCACATCACTTAATAG

>NZ_CP014150|3|3|1163912-1164027|CRISPRCasFinder
GCTTTAACGTTTCGTCAAATTGATATAACCACATCACTTAATAG	TTACTAAACTGCATTTGGGAAGTAGAAA
GCTTTAACGTTTCGTCAAATTGATATAATCACATCACTTAATAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014150.1\|WP_101508413.1\|1161779_1161998_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|224393
NZ_CP014150.1\|WP_101508423.1\|1172969_1173980_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|369561
NZ_CP014150.1\|WP_055329278.1\|1160733_1161192_-\|ImmA/IrrE-family-metallo-endopeptidase	unknown	unknown	gnl\|CDD\|368753
NZ_CP014150.1\|WP_101508414.1\|1162015_1162828_+\|phage-antirepressor-KilAC-domain-containing-protein	unknown	unknown	gnl\|CDD\|377029
NZ_CP014150.1\|WP_021128552.1\|1156923_1157190_+\|mor-transcription-activator-family-protein	unknown	unknown	gnl\|CDD\|337191
NZ_CP014150.1\|WP_021128554.1\|1154462_1155257_-\|YitT-family-protein	unknown	unknown	gnl\|CDD\|224203
NZ_CP014150.1\|WP_101508415.1\|1162862_1163855_+\|YqaJ-viral-recombinase-family-protein	unknown	unknown	gnl\|CDD\|227668
NZ_CP014150.1\|WP_101508412.1\|1157618_1160696_+\|collagenase	unknown	unknown	gnl\|CDD\|366791
NZ_CP014150.1\|WP_055332104.1\|1174710_1175043_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_101508420.1\|1167707_1168358_+\|DUF1311-domain-containing-protein	unknown	unknown	gnl\|CDD\|377758
NZ_CP014150.1\|WP_158645325.1\|1164852_1165596_+\|recombinase-RecT	unknown	unknown	gnl\|CDD\|236628
NZ_CP014150.1\|WP_101508419.1\|1166521_1167274_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|180750
NZ_CP014150.1\|WP_021128549.1\|1161210_1161612_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|238045
NZ_CP014150.1\|WP_021123572.1\|1155596_1155971_+\|CGGC-domain-containing-protein	unknown	unknown	gnl\|CDD\|378059
NZ_CP014150.1\|WP_101508422.1\|1170608_1172348_-\|ABC-F-family-ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|223562
NZ_CP014150.1\|WP_158645324.1\|1164441_1164609_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_101508421.1\|1168657_1170538_+\|caspase-family-protein	unknown	unknown	gnl\|CDD\|334197
NZ_CP014150.1\|WP_101508418.1\|1165722_1166610_+\|DnaD-domain-protein	unknown	unknown	gnl\|CDD\|273630
NZ_CP014150.1\|WP_101508424.1\|1174054_1174636_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_055329280.1\|1156111_1156630_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP014150.1\|WP_101508413.1\|1161779_1161998_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|224393	COG1476, COG1476, Predicted transcriptional regulators [Transcription].	2.56914e-13
NZ_CP014150.1\|WP_101508423.1\|1172969_1173980_+\|alpha/beta-hydrolase	gnl\|CDD\|369561	pfam07859, Abhydrolase_3, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	3.55022e-67
NZ_CP014150.1\|WP_055329278.1\|1160733_1161192_-\|ImmA/IrrE-family-metallo-endopeptidase	gnl\|CDD\|368753	pfam06114, Peptidase_M78, IrrE N-terminal-like domain. This entry includes the catalytic domain of the protein ImmA, which is a metallopeptidase containing an HEXXH zinc-binding motif from peptidase family M78. ImmA is encoded on a conjugative transposon. Conjugating bacteria are able to transfer conjugative transposons that can, for example, confer resistance to antibiotics. The transposon is integrated into the chromosome, but during conjugation excises itself and then moves to the recipient bacterium and re-integrate into its chromosome. Typically a conjugative tranposon encodes only the proteins required for this activity and the proteins that regulate it. During exponential growth, the ICEBs1 transposon of Bacillus subtilis is inactivated by the immunity repressor protein ImmR, which is encoded by the transposon and represses the genes for excision and transfer. Cleavage of ImmR relaxes repression and allows transfer of the transposon. ImmA has been shown to be essential for the cleavage of ImmR. This domain is also found in in metalloprotease IrrE, a central regulator of DNA damage repair in Deinococcaceae, HTH-type transcriptional regulators RamB and PrpC.	1.75074e-17
NZ_CP014150.1\|WP_101508414.1\|1162015_1162828_+\|phage-antirepressor-KilAC-domain-containing-protein	gnl\|CDD\|377029	pfam03374, ANT, Phage antirepressor protein KilAC domain. This domain was called the KilAC domain by Iyer and colleagues.	5.2887e-22
NZ_CP014150.1\|WP_021128552.1\|1156923_1157190_+\|mor-transcription-activator-family-protein	gnl\|CDD\|337191	pfam08765, Mor, Mor transcription activator family. Mor (Middle operon regulator) is a sequence specific DNA binding protein. It mediates transcription activation through its interactions with the C-terminal domains of the alpha and sigma subunits of bacterial RNA polymerase. The N terminal region of Mor is the dimerization region, and the C terminal contains a helix-turn-helix motif which binds DNA.	8.04073e-13
NZ_CP014150.1\|WP_021128554.1\|1154462_1155257_-\|YitT-family-protein	gnl\|CDD\|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	1.08564e-65
NZ_CP014150.1\|WP_101508418.1\|1165722_1166610_+\|DnaD-domain-protein	gnl\|CDD\|273630	TIGR01446, replication_protein, DnaD and phage-associated domain. This model represents the conserved domain of DnaD, part of Bacillus subtilis replication restart primosome, and of a number of phage-associated proteins. Members, both chromosomal or phage-associated, are found in the Bacillus/Clostridium group of Gram-positive bacteria. [DNA metabolism, DNA replication, recombination, and repair, Mobile and extrachromosomal element functions, Prophage functions].	8.92561e-05
NZ_CP014150.1\|WP_101508412.1\|1157618_1160696_+\|collagenase	gnl\|CDD\|366791	pfam01752, Peptidase_M9, Collagenase. This family of enzymes break down collagens.	2.28185e-69
NZ_CP014150.1\|WP_101508420.1\|1167707_1168358_+\|DUF1311-domain-containing-protein	gnl\|CDD\|377758	pfam07007, LprI, Lysozyme inhibitor LprI. This family consists of several bacterial proteins of around 120 residues in length. Members of this family contain four highly conserved cysteine residues. Family members include lipoprotein LprI from Mycobacterium, which binds to and inhibits macrophage lysozyme, which may aid bacterial survival.	2.70927e-12
NZ_CP014150.1\|WP_158645325.1\|1164852_1165596_+\|recombinase-RecT	gnl\|CDD\|236628	PRK09846, recT, recombination protein RecT.	2.6819e-74
NZ_CP014150.1\|WP_101508419.1\|1166521_1167274_+\|ATP-binding-protein	gnl\|CDD\|180750	PRK06921, PRK06921, hypothetical protein; Provisional.	1.6059e-59
NZ_CP014150.1\|WP_021128549.1\|1161210_1161612_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	2.71669e-15
NZ_CP014150.1\|WP_021123572.1\|1155596_1155971_+\|CGGC-domain-containing-protein	gnl\|CDD\|378059	pfam08821, CGGC, CGGC domain. This putative domain contains a quite highly conserved sequence of CGGC in its central region. The domain has many conserved cysteines and histidines suggestive of a zinc binding function.	1.38897e-24
NZ_CP014150.1\|WP_101508422.1\|1170608_1172348_-\|ABC-F-family-ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|223562	COG0488, Uup, ATPase components of ABC transporters with duplicated ATPase domains [General function prediction only].	1.77355e-111
NZ_CP014150.1\|WP_101508421.1\|1168657_1170538_+\|caspase-family-protein	gnl\|CDD\|334197	pfam00656, Peptidase_C14, Caspase domain.	2.54085e-28
NZ_CP014150.1\|WP_101508415.1\|1162862_1163855_+\|YqaJ-viral-recombinase-family-protein	gnl\|CDD\|227668	COG5377, COG5377, Phage-related protein, predicted endonuclease [DNA replication, recombination, and repair].	4.39654e-60

>NZ_CP014150.1|WP_101508415.1|1162862_1163855_+|YqaJ-viral-recombinase-family-protein
MRKYLDAIISHETKYMTKEEWLEARRGGIGGSDASSVLGFNPYKSSISVYLEKIQHNNLSKDLERKGGISLINKNQFKEEVSYKMELGNKLEEFVAREFTLKTGKKVRNINGILKNDNYPFALANIDRAVVGEKAFLECKVTNSFSKKLWKKEVPMHYQIQMTHYMAITGATHCYVAALIGNEDLVIHKIYRDEELISKVMNLEKRFWDECVLGESLPNPDGSNDYSNMLQGIYKDSKKEELILFEKDDLMSRYDEVCELSKDIYKEKKTIEQYIQSQMKDYEVAYLGDRKITWKTQIRSSLDSKKLKKEYPELVDRYMETTTSRVFRMS
>NZ_CP014150.1|WP_101508414.1|1162015_1162828_+|phage-antirepressor-KilAC-domain-containing-protein
MEIFKSKEFGDLRLIVVNGKEYFDAIPIAKTLGYSNPHDALMRHCQKEGVVFHEVGVETGKYKSGDSIMQFVSKKFIDEGNLYRLILKSKLKKVRKFEMWVFEEVLPTIRKHGAYINEDVIDEILDDPILLRKLTERLSNEKSKRYEAERKVNLLKGNIISNKPYVDFSKTVSNVEGAISIGSFAKLLNNNYINIGRNRLYHWFRENGYLIKSGKEKNNPKQKYIDMGLFRVVERVVQTENGDKLIITPLITGKGQIYFMEIIEEDFILN
>NZ_CP014150.1|WP_101508413.1|1161779_1161998_+|helix-turn-helix-domain-containing-protein
MIYKNNLKGIRVSRGLTQGDLAKLINMPRSTYIKKENEKSYFNIKEAMKIGKVLNLSIDYIFLTQSYQIGKK
>NZ_CP014150.1|WP_021128549.1|1161210_1161612_-|helix-turn-helix-transcriptional-regulator
METLSTRLKELRKEKGYTLEQMAQDLNTTKVTLSRYENGTREPKSETLNQLSDYFNVSIDYLFGKTDERNPKTKDEIIDVKKAIEEIKDELENSNSLMFDGECLSEDAISSLLSAMEVGLSIAKKKQEEMKNK
>NZ_CP014150.1|WP_055329278.1|1160733_1161192_-|ImmA/IrrE-family-metallo-endopeptidase
MGILDKIKDSIKGLVNKNKTRNPFELAEALGIILVEAPLKDGLNGCYHERSGFQFIYINSDLPYEKRLMVAAHELGHAILHRGRNILYLSNNTYYTRGTFEREANLFAAELLLEDDFFEKYKHIENCTLEYVSQCECVSYELVDYKLKYLSE
>NZ_CP014150.1|WP_101508412.1|1157618_1160696_+|collagenase
MKYKNHAKYIAGTLICSFGVTTIQSPILSHAMDSKNAKNINMFNNNDKEVRNTTNQNNKDKADRLTAEEASVHKKDKMIGKQSIDNVKKDKKSINYTMADLNKMSNEELIKTLEQINWYNITDLFEYNKDAQEFYGNREKFDFLIKTLEQKGTKYTSQNHEGIPTFVEVIRAGFYLGFYNEGLSYLYELETREKCLPAMISIQKNPNFKLGENGQNEVIKSLGMLIGNSAVSVDVVNNMIPVFEQYNQDLKNNMNNFGKSDIIYNIMKGVEYRLNAYAYDSKLQPEETQFAKKIDKYIDIVSDYMSNKPENDSEEWFIECGMYYTSKLYKFHSKPNQIHAKMDKVLEINEEMSWLYLKAVDLIEWYMGGTLSDGTPINSKEIKEKAKKYYLPNEYKFEDDKIVIKTGDKVTAEKVERLYWATKEVQSQFFKIIGSDKALEVGHADDILTVVIYNSPKEYKMNQVLYGYSTDNGGMYIEGEGTFYTYERTPQESIYSLEELFRHEYTHYLQSRYLIEGYFGTGDFYKDKDWRITWFEEGSAEFWAGATRTDNVISRKSMVSGISKNPSDRFTVDKLMHSKYGSWDFYNYGFAFVDFIYRERPEIFEKFTDLMITNNVAGYDKYVEELSKDVELNKGYQAYMQKLVDNYDNLTVPFVSDNYLKEHPSRDISKIKEDIDKTINLKNSKVETKKKATLNKYKVSGKRGKSSIESEKSPLFNTYTFSGIFEGGKSNGRTSDNKEMGEILNTTLKKLEQIGWSGYETVNAYHTDYKVNENGNYEFRIVFTGILPKGSQEVVNDDTFETANGPIKINTNYSGDLSDTDNKDYYYFNLYNPSNINITLENLDNKGVSWQLFHESDLNNYVAYPTTSGAVLNGDYNATKTGKYYILVYNHDKSIANYNLKVNFGNSNDDGVEQEDNNSFEKANPFNINQLIKGELDNSKDTSDYFKFEVKEDASLNISLEKTEGDGVNWLLFKDSDLENYIASPTESIDNKLNGKVDLKVGTYYLEVYGYGSSPVKYNFKVTPN
>NZ_CP014150.1|WP_021128552.1|1156923_1157190_+|mor-transcription-activator-family-protein
MLEKLKIEDLPDSYKDVAEEIGIDSFKKLVKLLGGNSLYIPKEVSLTRPIRDRIIKEDFNGDYKILSRRYNISQSQIRNILDKQTKGV
>NZ_CP014150.1|WP_055329280.1|1156111_1156630_+|hypothetical-protein
MKKIGIIITLILLVISLVGCENSESKKAVEQGKVEMNNKEYDKALASFKVALDKDSGNEEAKRLTTLINNYNKANVEFEKDNIDDANKFMNQIDEGTIEDSIKNDIDNLKAKIHEQEKIDKEIVHIKELIKDKKYEESKKSIDKIDSDKLTNKDKKEIDELKDEIYLGLLQI
>NZ_CP014150.1|WP_021123572.1|1155596_1155971_+|CGGC-domain-containing-protein
MKKVAIYVCGEVSRKCTANGCLRTFNAMEDSFERYKEDGCKLVAFNTCNGCDQDPVESLDVKIEKLKKADVEVMHISTCIRGRCSHYEEYAKEFAKHFEVIGYTHGSKEGKKNNNINYIKDIEK
>NZ_CP014150.1|WP_021128554.1|1154462_1155257_-|YitT-family-protein
MSVGLNMFLEPYMIASGGLTGLAIVLKNLFNTPLWFINLVFNIPLFIFGIKILGKRDAIKTLIGILFLTFFLKVTEPLTSAFQTNDVLLSSIAGGIVVGISLGMLFRIDASTGGTELACLILNKIFPFISISVFMFIIDGLVIALAGLVSRNIQIALYAIVSLYISVKICDTIVEGFDFSKSFIIVTDHSDEISDSIMENLERGVTFLEGRGGYSKQRKDVILVVVSRREEVVLRKLVNEIDPLAFVIINNAYEVLGEGFTRKV
>NZ_CP014150.1|WP_158645324.1|1164441_1164609_+|hypothetical-protein
MSKLKSALQSKEAKGEGLTVSKSYAMKQLMIKMNRITIIKTSICFNRGDRLLDSL
>NZ_CP014150.1|WP_158645325.1|1164852_1165596_+|recombinase-RecT
MSKLKSALQGKEAKGDGLTVSKSYAMKQLMIKMKNDIKEALPSHFCIDNFQKSAINTYNLDKSLQECEATTFISAMIECAKLGLEPNNILGQAYLVPVCVDGVNKVEFQIGYKGLIELAYRSGKIKSLYANEVFEKDEFHIDYGLDQKLIHKPFLGGDRGEVIGYYAVYQMDNRGASFVFMTRDEILGHSKKYSRSFGWDLWESEFDAMAKKTVIKKLLKYAPLSIELQKSVSIDESVGDSSCIGVI
>NZ_CP014150.1|WP_101508418.1|1165722_1166610_+|DnaD-domain-protein
MAVYRHIHIDFWQDGFVLDLTPEEKYFYMYLMTNSKTSQCGIYELPKRIIETETGYNRETVEKLISRFKEYEKIIYCEETKEIFLLNWMKHNKANSPQVKKCIEKELNKIKNKEFIGVFLDVCKEIKYSIDTLSIDYGEKEKEKEKEEKKEKQKYKEKDENEKINLSMYIKNNISQYAKLYEENIGLINGIASEWLIEVSENVDVRLFKKALEIATCNSCCNQGYVNGILKQWRSNNIRSLEDLNAYKLNKDKKGGANHDKYQRAVDEEEQELYRKPTEKELKEFKKFLEENTKL
>NZ_CP014150.1|WP_101508419.1|1166521_1167274_+|ATP-binding-protein
MKRNKNFIESQQKKSLKNLKSSLKKTQSYNCDKCRDLTFILDGDVAVSCDCRSLRQTESILKLSGISEEFRKKTFDSFNYAYDIQTIDAYSKAIGYYSSFLDIRSSRKNSIMFLGQVGSGKTHLSLAIANKLMDDGFGVLYMQYRDVITRIKQNVMNGEEYERIVNRYKNAKVLLMDDLFKGSISKSDVNIVFEIVNFRYFNNLPVIVSCEKGVDELLDIDEAIGSRLIEMSKDYLVEMKGRKLNFRVYG
>NZ_CP014150.1|WP_101508420.1|1167707_1168358_+|DUF1311-domain-containing-protein
MKKVIISIGLIMALILTGCAKDEKKENEKVATVVYCNNCGKESKEVTKFCSNCGKEAKWLAEKPEISKDKKEDTEKKDIDKKDENKDTTKDVETVKHSYKNEYINKLNSTEEGMSDLDYLYENGTTGEMGQAEATKLKRWDNMLNEIYSLLKTQLTESEMNELRNKQRSWIEYRDKTAENEASENTGGTLYNVVYNGSLARLTKERCYELVNTYMK
>NZ_CP014150.1|WP_101508421.1|1168657_1170538_+|caspase-family-protein
MSKKALLIGNKEYEGDDFEELNLPENDVRQLKDTLQIIGFEVLDKYNLKFNDMKNIISEFIGSINDGDEIIFYFSGHGYSYKGNNYILPIDCLDIIKINDLNVFKNGYSEAAKVIDVSSIVSDLKSNKNGINILLLDACRKEYKDKKYKSDKISYFTEISTYETSCFISYATALGKYSYENKNAKYSNYVDAICNVIYRKDQTLEEMFQCVRNFIKSTADYEINESEQRPCYVNSLNSSYSLINNDNYTPYLENKYFKDLFKIYKCLLSCYPEDGIDDEEKFNEALEFAKMELFYPQEILEKYMRKFIKGTEAKLGIINFILEDDNVRDVSVFRDRIFINRNFNIKNFDKEYYNFDDCIKFIEGLEAKSEELLYKVYYYNKKNIIVINASNEVSFQIIGNSKQANLYDLIHNPIKLISKDDKGKHITDTIIKYIKDKKNILLLGAYDTLKEDMVSAFSNYFRINDKILNIVEDIDIDIKYGQVDKLSSDVDSILQKDDREYYDYIKKVKEKKFDRILYPYKSFRHVRNERKILEDLLDIKDSQLIIYMDHKSDYFGENLNKNNISHYGDFIYKVDLVIYISKICAIENSIVKCIYEKVNNEIKRSIVVDIDYIKLGRINQKECSKK
>NZ_CP014150.1|WP_101508422.1|1170608_1172348_-|ABC-F-family-ATP-binding-cassette-domain-containing-protein
MIKIDNLSYSFPQRDLYNKVSFTLEDGQHCAFIGASGSGKSTLIDIIMDPEKYMFDGNLEMDPNLRIGYVSQFSQLDKIKEITVFEYIAQEFIKLQDEIASICSEMENSTDIDALLEKYQEALDAFDAIDGDDYESNINKKLNVANLAKHKDKMISELSGGEFKLIQVIKEMLNNPDLMIMDEPDVFLDFENLNALKDLINSHKKTILVITHNRYLLNHCFNKIIHLENTELQEFDGRYIDYNFALLQTKIELQEMSIADEEEIARNEALIEILREKATYNAEASRGRALKARVKIQERLEAKRIKAPFVDIKQPYINLETNNEIEETIALEACDFGVSFDEVLLENVNFDIKSTDKVAIVGTNGVGKTTLLKEIFKNNNESIKINENIKLAYLSQMQSEVVNESNTILQEFYDVGFETYGEIRKYVSRYGFDSDILTQKIESLSGGEKNILQLAKVSASKANMLLMDEPTSHLDIYSQMALEKAIADYKGAILMISHDYHFIVNCADYVLLIEDKTVRKMSMRKFRKMIYANHFDKDYLQIEEKKKAVEMEIASALKDTDFERAKILSTKLEELIKSL
>NZ_CP014150.1|WP_101508423.1|1172969_1173980_+|alpha/beta-hydrolase
MKKRFVISAGIAGLIGLWFYYRDKKYPLTKGYYLMNKFSVPDKVVTLSNVKLVNKLLSKEELPKTPDDITREIRYIKTEDKESIPLSIYKLKDMNSNIPCLIYFHGGGFFFKDEAYMHRLVCEYVKKAKCMVVFVHYRTSDEYPFPTPFKDCCNAIEYIWENAKQLNVNKKKIALGGDSAGGALTGSCTLWCRDETDIKPCFQMLIYPVTDLRMQTESMKKYSDCPLWNPSLTKKMWKFYLRNGIKGKKEYISPILAKRFSKLPPAYIETAQYDCIHDEGIDYAKSLKSAGVKVQLEDIKSVFHGYDVFLNTEITKKMIEKRAQALYSAFYDKDKD
>NZ_CP014150.1|WP_101508424.1|1174054_1174636_+|hypothetical-protein
MAYLLKIEQFERSYDIGVFKSEESIYKFIESIPFVKKEVFSDNYINYFMNFKDIPDYYEVNYNNYIYIISKFSFIPDEGEIYFNWREIHLWDEKESVKETFIEGETIVDAYSFSNNEVKSYIEKREELYKETKKYYESKGLKITRNALGSEDGEYVELLNDSILYLLDPRAVEIWEESKDIEEFMDKYKKYEY
>NZ_CP014150.1|WP_055332104.1|1174710_1175043_+|hypothetical-protein
MKKNVFGNFIPIITMLVVIILGVGFNLKGVFIIGLVGIVPLSFFIEGVMCSRKKIGFIIPLITSLTAFFIVILIYMNDSANVYLKYCLIAYILGYLFEKMISNIIKFFNR

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_CP014150_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP014150_4

1538341-1538445

Orphan

Consensus_repeat	Method
AACTGATCCAAATCAGCCAGCAACTGATCCAAATCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP014150_4

>merge|NZ_CP014150|4|1538341-1538445|CRISPRCasFinder
ACCAACTGAGGAACAACCACCAACTGATCCAAATCAGCCAGCAACTGATCCAAATCAGCCAACGCCACCAACTGATCCAAATCAGCCAGTAACTGATCCAAATCA

>NZ_CP014150|4|4|1538341-1538445|CRISPRCasFinder
ACCAACTGAGGAACAACCACCAACTGATCCAAATCA	GCCAGCAACTGATCCAAATCAGCCAACGCCACC
AACTGATCCAAATCAGCCAGTAACTGATCCAAATCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014150.1\|WP_021127207.1\|1528307_1529288_+\|TDT-family-transporter	unknown	unknown	gnl\|CDD\|187765
NZ_CP014150.1\|WP_057536118.1\|1545787_1546645_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224098
NZ_CP014150.1\|WP_055329009.1\|1531119_1532064_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377527
NZ_CP014150.1\|WP_155486422.1\|1534762_1534939_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_057536117.1\|1544589_1545795_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|183238
NZ_CP014150.1\|WP_055331869.1\|1529777_1530455_+\|glucosaminidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|376625
NZ_CP014150.1\|WP_101508601.1\|1538663_1539659_-\|calcium/sodium-antiporter	unknown	unknown	gnl\|CDD\|273039
NZ_CP014150.1\|WP_101508599.1\|1532066_1533215_+\|DUF2974-domain-containing-protein	unknown	unknown	gnl\|CDD\|238287
NZ_CP014150.1\|WP_057562467.1\|1533304_1534735_+\|PTS-transporter-subunit-EIIC	unknown	unknown	gnl\|CDD\|273920
NZ_CP014150.1\|WP_055328999.1\|1547437_1548472_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|226361
NZ_CP014150.1\|WP_054629708.1\|1539895_1540831_-\|magnesium-transporter-CorA-family-protein	unknown	unknown	gnl\|CDD\|213361
NZ_CP014150.1\|WP_021127200.1\|1535136_1535388_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_101508597.1\|1527844_1528294_+\|C-GCAxxG-C-C-family-protein	unknown	unknown	gnl\|CDD\|378246
NZ_CP014150.1\|WP_055329003.1\|1542525_1543026_+\|QueT-transporter-family-protein	unknown	unknown	gnl\|CDD\|377623
NZ_CP014150.1\|WP_101508602.1\|1541194_1542325_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|224370
NZ_CP014150.1\|WP_101508596.1\|1527390_1527639_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_101508598.1\|1530542_1530995_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378897
NZ_CP014150.1\|WP_021127193.1\|1544085_1544517_+\|rhodanese-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|238089
NZ_CP014150.1\|WP_101508603.1\|1543048_1543924_+\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|277331
NZ_CP014150.1\|WP_021127190.1\|1546653_1547436_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224098

Protein	Function_ID	Function_description	E-value
NZ_CP014150.1\|WP_021127207.1\|1528307_1529288_+\|TDT-family-transporter	gnl\|CDD\|187765	cd09325, TDT_C4-dicarb_trans, C4-dicarboxylate transporters of the Tellurite-resistance/Dicarboxylate Transporter (TDT) family. This subfamily contains bacterial C4-dicarboxylate transporters, which is part of the Tellurite-resistance/Dicarboxylate Transporter (TDT) family. It includes Tellurite resistance protein tehA; the tehA gene encodes an integral membrane protein that has been shown to have efflux activity of quaternary ammonium compounds. TehA protein of Escherichia coli functions as a tellurite-resistance uptake permease.	1.59014e-66
NZ_CP014150.1\|WP_057536118.1\|1545787_1546645_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224098	COG1177, PotC, ABC-type spermidine/putrescine transport system, permease component II [Amino acid transport and metabolism].	1.86663e-28
NZ_CP014150.1\|WP_055331869.1\|1529777_1530455_+\|glucosaminidase-domain-containing-protein	gnl\|CDD\|376625	pfam01832, Glucosaminidase, Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase. This family includes Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase EC:3.2.1.96. As well as the flageller protein J that has been shown to hydrolyze peptidoglycan.	2.33891e-07
NZ_CP014150.1\|WP_101508598.1\|1530542_1530995_-\|hypothetical-protein	gnl\|CDD\|378897	pfam12638, Staygreen, Staygreen protein. This family of proteins have been implicated in chlorophyll degradation. Intriguingly members of this family are also found in non-photosynthetic bacteria.	2.26427e-31
NZ_CP014150.1\|WP_057536117.1\|1544589_1545795_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|183238	PRK11622, PRK11622, ABC transporter substrate-binding protein.	3.57226e-159
NZ_CP014150.1\|WP_054629708.1\|1539895_1540831_-\|magnesium-transporter-CorA-family-protein	gnl\|CDD\|213361	cd12827, EcCorA_ZntB-like_u2, uncharacterized bacterial subfamily of the Escherichia coli CorA-Salmonella typhimurium ZntB family. A uncharacterized subfamily of the Escherichia coli CorA-Salmonella typhimurium ZntB (EcCorA-ZntB_like) family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes.The EcCorA-ZntB-like family includes the Mg2+ transporters Escherichia coli and Salmonella typhimurium CorAs, which can also transport Co2+, and Ni2+. Structures of the intracellular domain of EcCorA-ZntB-like family members, Vibrio parahaemolyticus and Salmonella typhimurium ZntB, form funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport through Salmonella typhimurium CorA. Natural variants such as GVN and GIN, such as occur in some ZntB family proteins, may be associated with the transport of different divalent cations, such as zinc and cadmium. The functional diversity of MIT transporters may also be due to minor structural differences regulating gating, substrate selection, and transport.	1.18419e-125
NZ_CP014150.1\|WP_101508601.1\|1538663_1539659_-\|calcium/sodium-antiporter	gnl\|CDD\|273039	TIGR00367, Uncharacterized_membrane_protein_MJ0091, K+-dependent Na+/Ca+ exchanger related-protein. This model models a family of bacterial and archaeal proteins that is homologous, except for lacking a central region of ~ 250 amino acids and an N-terminal region of > 100 residues, to a functionally proven potassium-dependent sodium-calcium exchanger of the rat. [Unknown function, General].	3.48147e-69
NZ_CP014150.1\|WP_101508599.1\|1532066_1533215_+\|DUF2974-domain-containing-protein	gnl\|CDD\|238287	cd00519, Lipase_3, Lipase (class 3). Lipases are esterases that can hydrolyze long-chain acyl-triglycerides into di- and monoglycerides, glycerol, and free fatty acids at a water/lipid interface. A typical feature of lipases is "interfacial activation," the process of becoming active at the lipid/water interface, although several examples of lipases have been identified that do not undergo interfacial activation . The active site of a lipase contains a catalytic triad consisting of Ser - His - Asp/Glu, but unlike most serine proteases, the active site is buried inside the structure. A "lid" or "flap" covers the active site, making it inaccessible to solvent and substrates. The lid opens during the process of interfacial activation, allowing the lipid substrate access to the active site. .	4.20976e-07
NZ_CP014150.1\|WP_057562467.1\|1533304_1534735_+\|PTS-transporter-subunit-EIIC	gnl\|CDD\|273920	TIGR01998, N-acetylglucosamine_and_glucose_PTS, PTS system, N-acetylglucosamine-specific IIBC component. This model represents the combined B and C domains of the PTS transport system enzyme II specific for N-acetylglucosamine transport. Many of the genes in this family also include an A domain as part of the same polypeptide and thus should be given the name "PTS system, N-acetylglucosamine-specific IIABC component". This family is most closely related to the glucose-specific PTS enzymes. [Transport and binding proteins, Carbohydrates, organic alcohols, and acids].	4.63792e-171
NZ_CP014150.1\|WP_055328999.1\|1547437_1548472_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	1.40039e-133
NZ_CP014150.1\|WP_021127193.1\|1544085_1544517_+\|rhodanese-like-domain-containing-protein	gnl\|CDD\|238089	cd00158, RHOD, Rhodanese Homology Domain (RHOD); an alpha beta fold domain found duplicated in the rhodanese protein. The cysteine containing enzymatically active version of the domain is also found in the Cdc25 class of protein phosphatases and a variety of proteins such as sulfide dehydrogenases and certain stress proteins such as senesence specific protein 1 in plants, PspE and GlpE in bacteria and cyanide and arsenate resistance proteins. Inactive versions (no active site cysteine) are also seen in dual specificity phosphatases, ubiquitin hydrolases from yeast and in sulfuryltransferases, where they are believed to play a regulatory role in multidomain proteins.	7.66621e-28
NZ_CP014150.1\|WP_101508597.1\|1527844_1528294_+\|C-GCAxxG-C-C-family-protein	gnl\|CDD\|378246	pfam09719, C_GCAxxG_C_C, Putative redox-active protein (C_GCAxxG_C_C). This entry represents a putative redox-active protein of about 140 residues, with four perfectly conserved Cys residues. It includes a CGAXXG motif. Most members are found within one or two loci of transporter or oxidoreductase genes. A member from Geobacter sulfurreducens, located in a molybdenum transporter operon, has a TAT (twin-arginine translocation) signal sequence for Sec-independent transport across the plasma membrane, a hallmark of bound prosthetic groups such as FeS clusters.	4.86267e-28
NZ_CP014150.1\|WP_055329003.1\|1542525_1543026_+\|QueT-transporter-family-protein	gnl\|CDD\|377623	pfam06177, QueT, QueT transporter. This family includes the queT gene encoding a hypothetical integral membrane protein with 5 predicted transmembrane regions. The queT genes in Firmicutes are often preceded by the PreQ1 (7-aminomethyl-7-deazaguanine) riboswitches of two distinct classes, suggesting involvement of the QueT transporters in uptake of a queuosine biosynthetic intermediate.	1.49285e-41
NZ_CP014150.1\|WP_101508602.1\|1541194_1542325_+\|aldo/keto-reductase	gnl\|CDD\|224370	COG1453, COG1453, Predicted oxidoreductases of the aldo/keto reductase family [General function prediction only].	4.28254e-173
NZ_CP014150.1\|WP_101508603.1\|1543048_1543924_+\|metallophosphoesterase	gnl\|CDD\|277331	cd07385, MPP_YkuE_C, Bacillus subtilis YkuE and related proteins, C-terminal metallophosphatase domain. YkuE is an uncharacterized Bacillus subtilis protein with a C-terminal metallophosphatase domain and an N-terminal twin-arginine (RR) motif. An RR-signal peptide derived from the Bacillus subtilis YkuE protein can direct Tat-dependent secretion of agarase in Streptomyces lividans. This is an indication that YkuE is transported by the Bacillus subtilis Tat (Twin-arginine translocation) pathway machinery. YkuE 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.	5.15529e-63
NZ_CP014150.1\|WP_021127190.1\|1546653_1547436_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224098	COG1177, PotC, ABC-type spermidine/putrescine transport system, permease component II [Amino acid transport and metabolism].	1.32975e-40
NZ_CP014150.1\|WP_055329009.1\|1531119_1532064_+\|hypothetical-protein	gnl\|CDD\|377527	pfam05580, Peptidase_S55, SpoIVB peptidase S55. The protein SpoIVB plays a key role in signalling in the final sigma-K checkpoint of Bacillus subtilis.	1.23513e-26

>NZ_CP014150.1|WP_021127200.1|1535136_1535388_-|hypothetical-protein
MNDSYLRRKAVEEAKSIYEDYFSASKTLDAFNSIPSIEVYAIPKYYHSTCCRCLNPYPHNEKNYFPNEGFICDDCLNNTNTLS
>NZ_CP014150.1|WP_155486422.1|1534762_1534939_-|hypothetical-protein
MHLTLDELQKDDQLFETDGYNIIINKRLATQINNVYISFGGLLSPNEFSIDCDFNEYY
>NZ_CP014150.1|WP_057562467.1|1533304_1534735_+|PTS-transporter-subunit-EIIC
MLKFLQRIGKSLMLPIATLPIAGIMLRLGQADVVNALGGIPFMQTILPFFGAAGSALFDNLPLLFALGVAVGFSDDQNGASALAGVISYFTLTNVTKQYWTMNLSSDLVSTLNISFLGGILAGLIGGLCYNKFRKVKLPEFLAFFGGRRLVPIMAGLISVIIAIPLGMIWPTVQGALTQFSMSIVGFGAVGAAIFGLFNRLLIPVGLHHVLNSFFWFQLGSYNGKTGDIARFFAGDPTAGHFMAGFFPIMMFGLPAIALAIYFAAKKEKRKAVGGMLLSLALTSFLTGVTEPIEFLFIFLSPMLLVAHAILTSLSFFIVDSLGILHGFTFSAGAIDYLMNFGLATNPLTLLLVGLGMGVLYFIVFYILIVKLNLPTPGREEDCDEFDQDGAQVSVSGDEAVAKKYVEFLGGSENIVKVENCATRLRLELLDTDKINEKGLKSIGAKGIVKLNKTSAQVIVGTNVEFVADGMKVFLK
>NZ_CP014150.1|WP_101508599.1|1532066_1533215_+|DUF2974-domain-containing-protein
MKIIKLTLILCLSICIIGFNKLDLLDENNPKWDIDSDKDGLPDAFEELIGTDKYNVDSDKDNINDEEEIKLGFDPNVRDLNRNYHYKLNNKYISDNFDLNNKISVTEKMIFESCQIVSEKFYENPTGKTVGEVFLDKYKSIKNFKIIRFERGENGFGAIALNLGDSIIVSYKPTRSFRDWIENFTTQFMPHPQRGYAIEFTEPIINKNVQIYTCGHSLGGLLAQYVTYDLVNKGYKNIKTITFNSANSFNPKHMQGKYAPPIIKSNLVKDYINVYIDVINQKDEGYIVDLTSINKFLIKSIDYNGFVDINNDKFKESDFKDYEEIVTNYITCNDPLYLTINGGYLGKCNIVNMNCGNLGFKRDIQELMKFHDLKNFSKIIEN
>NZ_CP014150.1|WP_055329009.1|1531119_1532064_+|hypothetical-protein
MKNFKTIIITAIIAILLPTNICFSQEKVEKLMPSAEVVFVNLNLKFPIVQSKLSKDSDFEEDDVILSVISLSKKKVYDLNDLTELYKQEDEKVLVRFIRDKKENSQVFTATDFRGIYLSFVQQFCGTITAIKEDGSFVGLSHNIEGSEAAQSTQVYETAYVHSIKAKLFNSGGLKPHIKEGKDGKLNYMGDIEGYSDYGVHGKLKENKFNSSKAMEIGRPKKGTAYIYCKSPITNEKKLHEIEIVKVYKDGAKIKVKDKELKEYRGGVIGGMSGSPIIQDNKLVGGVRSSYIYNHKVGFISNIDYMLNPNLSSK
>NZ_CP014150.1|WP_101508598.1|1530542_1530995_-|hypothetical-protein
MNFNPNKLKVNFINSDIINSQIKYRKYTLRYDFDLNNSFLDIANFYNYNKIDFTLRNEVLGEWILINKNKYTLCLYIYLKGYFPYEIKLKYEMFKAYLPNIIKSILYGDKNFIYINNFLLNSEIIVNFNSDSFMFNTSENYKKVKSYFIN
>NZ_CP014150.1|WP_055331869.1|1529777_1530455_+|glucosaminidase-domain-containing-protein
MKLLKKIVILVCLSSMLVGFNIGYKEKQDRLNIQNINNIKIRERQEDNNQFKISKMDEDNTLNISYLRDDVTLKTGITEDEMREVLINTTGAKTMSHLAKAFVDAENLYGVNAFFMAGVVALESGFATSRRAIEDNNLTGYEVYKDDSEGKLFTSQYESILQTAKHLKENYLTKDSIYYNGLSVDAVQINYCPDEGLNKNWNGKVNELANSFLNTYKVLYEFDKK
>NZ_CP014150.1|WP_021127207.1|1528307_1529288_+|TDT-family-transporter
MKTIRKEISKSDFQNIPIAIAGISLGFMSISTALVEFNIFWVRHLAVIFSSISILILLMKTFLHPKQVWEELKNPLAGSIYPTISMTIMLIAVYIVKLNLQFAKVLWIGATILHLVIFIMFTVHMLRNFKITNMLPSWFISTVGIGLAAVTSKPMEMPYLSRAIFYYSLILFIVLGIIMTYRLIFMEKLEGNKKFTLMIMTAPANICLAGYLAVYEKPNIVLLQILALLGYASIIYSFILLPRLINTKFTLALAPLTFPLGIGVTAAQRYIKYLNSIGSGMEEILRYILYIQVIVSVAVIGYIVIKTIDLFVKEFILIENNLERID
>NZ_CP014150.1|WP_101508597.1|1527844_1528294_+|C-GCAxxG-C-C-family-protein
MTKQSRVEEIRKIAEGYFERGEFYCSEAVVKTINDELGKPFGDDVTKLASGFPIGIGKSGCLCGAVSGGVIALGMVYGRCHKEPMNDKMFTASADLHDHIKKLYKSTCCRVMTRNFEFQSPERKAHCIKITGEVAAYIAEKLIEDDQLK
>NZ_CP014150.1|WP_101508596.1|1527390_1527639_+|hypothetical-protein
MGCPNCKCNKNKISEEEYNELKEYLEETIKDFKVIDYIDEDNQSNRFVEVELEDYILEVENVDTTNLNLAKLIDIIIQNKMV
>NZ_CP014150.1|WP_101508601.1|1538663_1539659_-|calcium/sodium-antiporter
MVYLFLLLGFLFLVKGADYFVDGSSSIAKYFKVPPLIIGLTIVAFGTSAPEAAVSITASIQGQNGIALGNVIGSNIFNLLCVVGMSAFISTLPVKKSILLKEFPFLLLSSIVLFILCNDFVFQKSSISILSSGDGLILLIFFIIFIYYLLGVALKSRKETKIDYDDLVLSKDNHSGNTCTCEISISKALIMSIVGIIGIILGGKLVVDCASDIAMTFGVSEKMIGLTIVSIGTSLPEFVTSVIAASKGESDIALGNVIGSNVFNILFILGLSSLISPIPVDPSLFFDIAIMILITIVTYLFSIRKKDVNKFESIILIAAYAIYMMLVIFKV
>NZ_CP014150.1|WP_054629708.1|1539895_1540831_-|magnesium-transporter-CorA-family-protein
MIRYYKTIDSKLEKLKSFENGCWINLVEPTTAEILDISTKFNIDIESIRAALDEEERSRIDIEDNHILILIDIPIDESDASSAHYSTIPLGIILLDNTIVTICTAQTKILNDFIVGHVKNFFTFKKTRFILQILYKNASYYLHYLRRINKMTIAIEKEIYKSMKNKELVQLLELEKSLIYFSTSLKANELVLNKMLRTESIKKYSEDEDLLEDVIIENKQALEMATIYGDILSRIMDAFSAIVSNNQNTVMQFLTSITLIMSIPTIVSGFFGMNVEGLPFSNHVNGFWIVILITCIMCLILTFIMSRNKLL
>NZ_CP014150.1|WP_101508602.1|1541194_1542325_+|aldo/keto-reductase
MRYREFGSTGEKISILGFGCMRFPQTDGKIDEDETLKMVRYAIDNGVNYIDTAYPYHGGESELVVGRILKDGYREKVNLATKLPSWNIKSREDMDKYLNEQLKKLQTNYIDFYLVHALDKELWDNLVKNGIFDFLDEIKRNKKVRYVGFSFHDKYEVFEKIIDDYDWDFTQIQYNYIDEDYQAGTKGLEYAYKKGLGIVIMEPLRGGKLVNNLSDDIKDIIKFANTKKSPTKWAFKFLYNKSEIGIVLSGMSTMEQVIENIKICDEEGKANSMTRDEKKIIDNLGEKFKSKIKVDCTACKYCIPCPRGVNIPGCFEALNNASMFDDVESVKINMYKFIEENESDASMCIECGKCEAMCPQHINIIDKLKEVKYTFK
>NZ_CP014150.1|WP_055329003.1|1542525_1543026_+|QueT-transporter-family-protein
MTNKTKKLVMTSLVAAIYAVLTLVLGAISYGPIQFRIAEIMVLLAFIKKDYIWGLTIGCFLANVIGPYGAPDIIFGTTATFLSVYAIYLTGKAMKGKKYAILIASIWPTLINAVIIGFMLNIFVGMPLILSMIQVGFGEFVVITIIGVPVYKIIGKKYIKLLENAF
>NZ_CP014150.1|WP_101508603.1|1543048_1543924_+|metallophosphoesterase
MFVEILIGSTIVLGTTLFLKNETEKLEITKHEVENNKIPKDFDGFKIIQISDLHNKSFGKNNEKLLKKVEDEKPDIVVITGDLVEGDNNKYHVALNLVEELTKKYEVYYIVGNHEQKSLIKKYKEEYKEYFKELEKKSIINLHNDKVCLNKGNSCINLFGFIVPLDYYPYFFKNYKNRKKDLEKNLICDSLGEIDKENYNIMLAHTPFFFEDYEKYGVDLVLSGHVHGGIIRIPGIGGVLSPNREFFPKYDFGKYEKNNTTMLLSKGLGGSKVLIRFNCKPEIVSIVLKSK
>NZ_CP014150.1|WP_021127193.1|1544085_1544517_+|rhodanese-like-domain-containing-protein
MKKNKKLKMLVMGLLFALSITSLVGCSSNKGNDTSSKSESSYKNINAKETEDLLASGDDIAVVDVRSKGEYDEGHIDRAQNIDFNDFENNLTILDDYKEKPVLLYCKTGNRSEKAAKILQKHGFKKVYNATDGVEEHDYKLVK
>NZ_CP014150.1|WP_057536117.1|1544589_1545795_+|ABC-transporter-substrate-binding-protein
MKKIIALVMTLSLIFMVGCSSNSAKNTEDILNKDQKEIEKLAKGSTVNFYGWGGNEVLNKWFDTYVIPNMKEKYDISVKRVGMDIDTIMNKLLSEKKLQNDNGNIDVFWLNGENFKSAKDNDLLFGPFTSKIENYEKYVDTKSKDITTDFGTPVDNMESPWGKATFTVFKNGEKVENQITDTKSLKEAIMKNPGKFTYPAPPDFTGSAFVRNIIYDTVGYEKVANLPEDEKQVKEAIQPAINYLNEIKPYLWNKGKTYPSTIAQLNNMYSDNEVYFSMSYSPNEVKGKIDSGEFNKNTQFINFDKGNISNTHFLAIPKNAKNKAGSMVLINYLTSIDAQASKSNPKNWGDMTILDLNKVPSEDRSKFKSSIDIKNPVPEIKASLVPIIEKIWIEEVANSNE
>NZ_CP014150.1|WP_057536118.1|1545787_1546645_+|ABC-transporter-permease-subunit
MSKFKPYLYIAPVAILLITIIGMGIFTCICQSLGYFPQIGMTDITLSYYKELLSDKQFVESIYISLRTALISSIISVLVGVILAYFISKEKFSKFRYFLINLPIIVPHIVVILLTFAIFSKSGIISRILYNLDLISDSNQFISLVNDKYGIGIILVYIYKGIPFIALTTYNILKSLDKNLEDVARNLGANNVQAFKFIILPQIIPSIISSFIIIFAFSFGSFEVPYLIGATSPKALPVNAYLYYIGSDLTKRPISMAMNTVLAGISFILLIIYDTIFKKIYKYKL
>NZ_CP014150.1|WP_021127190.1|1546653_1547436_+|ABC-transporter-permease-subunit
MSKKLKKLIVNIILLTLILPLGILFIWAITSSWVYPNLIPNEFSLRGFEYILNEENIKVLLNSIFISIVVVIITLIISIPAAKAISLYEFKGKKFFELLILSPIIIPMISVAMGIQLVFIKFGIANTLTGVILINIIPCIPYGVRIIADVYKLIGAKYEIQASMLGAKKIDTLRYVTIPLILPGIIGASSMCFIISFSQYFLTLLIGGGSVITYPLLMFPYIQSGDRILASMYSIVFIIISLIVVMLMKKSLEKYYNKEN
>NZ_CP014150.1|WP_055328999.1|1547437_1548472_+|ABC-transporter-ATP-binding-protein
MASVKIVNLTKSFNNVNVLNSINLDINQGEFITLLGKSGCGKSTTLKLIAGLISPDKGDILFDKNSILNQKTQERQAVIVFQDYSLFPHMNVFENIEFGLKMKKIEKKIRQKKVMELLELVKLDGFEKKFPSELSGGQKQRVAIARTLAVNPKVLLLDEPFSSLDINLRNEMRSFILELQKKLNITTVLVTHDKEEALMMSDKIAVMIDGNIAQFDSPMNLYEKPISKDIANVFGQRNYLKGKIKNGIFTSDIFDIELKGHENIDNIELMISREDVKIHNKKTYGLEGIISKKTYAGDTTYYEIDVKTKTIISSSSESFYNIGDEVSIDIKPKNIIYFKNNLKK

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Crispr_ID: NZ_CP014150_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP014150_5

2623659-2623744

Orphan

Consensus_repeat	Method
TTTAGCTTCTTCAACTTTAGTTTCTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP014150_5

>merge|NZ_CP014150|5|2623659-2623744|CRISPRCasFinder
TTCTATTTCTTGTTCTTTAGCTTCTTCAACTTTAGTTTCTTTTACTTCTATATTATCGGCTTTAATTTCTTCAGTTTTAGCCTCTT

>NZ_CP014150|5|5|2623659-2623744|CRISPRCasFinder
TTCTATTTCTTGTTCTTTAGCTTCTT	CAACTTTAGTTTCTTTTACTTCTATATTATCGGC
TTTAATTTCTTCAGTTTTAGCCTCTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP014150.1\|WP_021128119.1\|2615597_2616866_+\|DUF1002-domain-containing-protein	unknown	unknown	gnl\|CDD\|377628
NZ_CP014150.1\|WP_021128125.1\|2620064_2620550_-\|chemotaxis-protein-CheD	unknown	unknown	gnl\|CDD\|319352
NZ_CP014150.1\|WP_021128131.1\|2627743_2629678_-\|iron-hydrogenase-small-subunit	unknown	unknown	gnl\|CDD\|274171
NZ_CP014150.1\|WP_021128124.1\|2619564_2620047_-\|purine-binding-chemotaxis-protein-CheW	unknown	unknown	gnl\|CDD\|223905
NZ_CP014150.1\|WP_021128120.1\|2616945_2617209_-\|FliM/FliN-family-flagellar-motor-switch-protein	unknown	unknown	gnl\|CDD\|236154
NZ_CP014150.1\|WP_021128121.1\|2617213_2618101_-\|FliM/FliN-family-flagellar-motor-switch-protein	unknown	unknown	gnl\|CDD\|130464
NZ_CP014150.1\|WP_055328261.1\|2626820_2627426_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP014150.1\|WP_057562128.1\|2630935_2631955_-\|RIP-metalloprotease-RseP	unknown	unknown	gnl\|CDD\|308008
NZ_CP014150.1\|WP_021128135.1\|2633182_2633959_-\|phosphatidate-cytidylyltransferase	unknown	unknown	gnl\|CDD\|366491
NZ_CP014150.1\|WP_021128136.1\|2633971_2634706_-\|isoprenyl-transferase	unknown	unknown	gnl\|CDD\|184840
NZ_CP014150.1\|WP_038293377.1\|2618771_2619581_-\|protein-glutamate-O-methyltransferase-CheR	unknown	unknown	gnl\|CDD\|224271
NZ_CP014150.1\|WP_021128137.1\|2634942_2635500_-\|ribosome-recycling-factor	unknown	unknown	gnl\|CDD\|178850
NZ_CP014150.1\|WP_021128132.1\|2629842_2630904_-\|flavodoxin-dependent-(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase	unknown	unknown	gnl\|CDD\|377382
NZ_CP014150.1\|WP_021128129.1\|2624676_2626413_-\|HAMP-domain-containing-protein	unknown	unknown	gnl\|CDD\|214599
NZ_CP014150.1\|WP_101509066.1\|2631967_2633119_-\|1-deoxy-D-xylulose-5-phosphate-reductoisomerase	unknown	unknown	gnl\|CDD\|235472
NZ_CP014150.1\|WP_021128126.1\|2620561_2621176_-\|chemotaxis-protein-CheC	unknown	unknown	gnl\|CDD\|381737
NZ_CP014150.1\|WP_101509064.1\|2613636_2615361_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP014150.1\|WP_057547754.1\|2621193_2622267_-\|chemotaxis-response-regulator-protein-glutamate-methylesterase	unknown	unknown	gnl\|CDD\|234828
NZ_CP014150.1\|WP_021128122.1\|2618394_2618748_-\|response-regulator	unknown	unknown	gnl\|CDD\|381097
NZ_CP014150.1\|WP_021124639.1\|2634736_2634940_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP014150.1\|WP_021128119.1\|2615597_2616866_+\|DUF1002-domain-containing-protein	gnl\|CDD\|377628	pfam06207, DUF1002, Protein of unknown function (DUF1002). This protein family has no known function. Its members are about 300 amino acids in length. It has so far been detected in Firmicute bacteria and some archaebacteria.	7.82715e-94
NZ_CP014150.1\|WP_021128125.1\|2620064_2620550_-\|chemotaxis-protein-CheD	gnl\|CDD\|319352	cd16352, CheD, chemotaxis protein CheD stimulates methylation of methyl-accepting chemotaxis proteins. This family contains bacterial chemotaxis protein CheD that stimulates methylation of methyl-accepting chemotaxis proteins (MCPs). The CheD chemotaxis gene is not found in the Escherichia coli genome, but is present in many other organisms, including B. subtilis, where CheD appears to have two separate roles; it binds to chemoreceptors to activate them as part of the CheC/CheD/CheYp adaptation system, and it deamidates selected residues to activate chemoreceptors, enabling them to mediate amino acid chemotaxis. CheD has been shown to catalyze amide hydrolysis of specific glutaminyl side chains of the B. subtilis chemoreceptors McpA, McpB and McpC; deamination by CheD is required for the chemoreceptors to effectively transduce signals to the CheA kinase. CheD's ability to bind the receptors is controlled by CheC via a competitive binding mechanism; substituting Gln into the receptor motif of the signal-terminating phosphatase, CheC, turns the inhibitor into a receptor-modifying deamidase CheD substrate. Also, CheYp increases the affinity of CheD for CheC, controlling CheD binding to the receptors through its interactions with CheC. Thus, high levels of CheYp means CheC is a better binding target for CheD than the receptors, resulting in decreased CheA activity. The CheD structure reveals a distant homology with a class of bacterial toxins represented by the cytotoxic necrotizing factor 1 (CNF1) as well as a class of proteins of unknown function represented by B. subtilis YfiH. An invariant Cys-His pair forming a catalytic dyad is observed, and is required by the toxins for deamidation activity.	4.03164e-60
NZ_CP014150.1\|WP_021128131.1\|2627743_2629678_-\|iron-hydrogenase-small-subunit	gnl\|CDD\|274171	TIGR02512, Periplasmic_hydrogenase_large_subunit, [FeFe] hydrogenase, group A. This model describes iron-only hydrogenases of anaerobic and microaerophilic bacteria and protozoa. This model is narrower, and covers a longer stretch of sequence, than pfam02906. This family represents a division among families that belong to pfam02906, which also includes proteins such as nuclear prelamin A recognition factor in animals. Note that this family shows some heterogeneity in terms of periplasmic, cytosolic, or hydrogenosome location, NAD or NADP dependence, and overal protein protein length.	5.24495e-157
NZ_CP014150.1\|WP_021128124.1\|2619564_2620047_-\|purine-binding-chemotaxis-protein-CheW	gnl\|CDD\|223905	COG0835, CheW, Chemotaxis signal transduction protein [Cell motility and secretion / Signal transduction mechanisms].	7.38315e-31
NZ_CP014150.1\|WP_021128120.1\|2616945_2617209_-\|FliM/FliN-family-flagellar-motor-switch-protein	gnl\|CDD\|236154	PRK08119, PRK08119, flagellar motor switch protein; Validated.	1.99234e-25
NZ_CP014150.1\|WP_021128121.1\|2617213_2618101_-\|FliM/FliN-family-flagellar-motor-switch-protein	gnl\|CDD\|130464	TIGR01397, Flagellar_motor_switch_protein_FliM, flagellar motor switch protein FliM. Members of this family are the flagellar motor switch protein FliM. The family excludes FliM homologs that lack an N-terminal region critical to interaction with phosphorylated CheY. One set lacking this N-terminal region is found in Rhizobium meliloti, in which the direction of flagellar rotation is not reversible (i.e. the FliM homolog does not act to reverse the motor direction), and in related species. Another is found in Buchnera, an obligate intracellular endosymbiont with genes for many of the components of the flagellar apparatus, but not, apparently, for flagellin iself. [Cellular processes, Chemotaxis and motility].	1.00908e-38
NZ_CP014150.1\|WP_021128137.1\|2634942_2635500_-\|ribosome-recycling-factor	gnl\|CDD\|178850	PRK00083, frr, ribosome recycling factor; Reviewed.	2.39738e-107
NZ_CP014150.1\|WP_057562128.1\|2630935_2631955_-\|RIP-metalloprotease-RseP	gnl\|CDD\|308008	pfam02163, Peptidase_M50, Peptidase family M50.	1.98014e-71
NZ_CP014150.1\|WP_021128135.1\|2633182_2633959_-\|phosphatidate-cytidylyltransferase	gnl\|CDD\|366491	pfam01148, CTP_transf_1, Cytidylyltransferase family. The members of this family are integral membrane protein cytidylyltransferases. The family includes phosphatidate cytidylyltransferase EC:2.7.7.41 as well as Sec59 from yeast. Sec59 is a dolichol kinase EC:2.7.1.108.	2.83233e-48
NZ_CP014150.1\|WP_021128136.1\|2633971_2634706_-\|isoprenyl-transferase	gnl\|CDD\|184840	PRK14830, PRK14830, undecaprenyl pyrophosphate synthase; Provisional.	1.0485e-151
NZ_CP014150.1\|WP_038293377.1\|2618771_2619581_-\|protein-glutamate-O-methyltransferase-CheR	gnl\|CDD\|224271	COG1352, CheR, Methylase of chemotaxis methyl-accepting proteins [Cell motility and secretion / Signal transduction mechanisms].	7.62853e-85
NZ_CP014150.1\|WP_021128132.1\|2629842_2630904_-\|flavodoxin-dependent-(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase	gnl\|CDD\|377382	pfam04551, GcpE, GcpE protein. In a variety of organisms, including plants and several eubacteria, isoprenoids are synthesized by the mevalonate-independent 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway. Although different enzymes of this pathway have been described, the terminal biosynthetic steps of the MEP pathway have not been fully elucidated. GcpE gene of Escherichia coli is involved in this pathway.	0
NZ_CP014150.1\|WP_021128129.1\|2624676_2626413_-\|HAMP-domain-containing-protein	gnl\|CDD\|214599	smart00283, MA, Methyl-accepting chemotaxis-like domains (chemotaxis sensory transducer). Thought to undergo reversible methylation in response to attractants or repellants during bacterial chemotaxis.	2.47346e-57
NZ_CP014150.1\|WP_101509066.1\|2631967_2633119_-\|1-deoxy-D-xylulose-5-phosphate-reductoisomerase	gnl\|CDD\|235472	PRK05447, PRK05447, 1-deoxy-D-xylulose 5-phosphate reductoisomerase; Provisional.	0
NZ_CP014150.1\|WP_021128126.1\|2620561_2621176_-\|chemotaxis-protein-CheC	gnl\|CDD\|381737	cd17909, CheC_ClassI, chemotaxis protein CheC, Class I. This subfamily contains Class I CheC proteins with phosphatase activity. The Class I cheC genes are generally found in firmicute and archaeal chemotaxis operons with cheD, usually translationally coupled. Class I CheCs interact with the CheD protein which is responsible for deamidation of certain glutamine residues to glutamates on the chemotaxis receptor proteins. This family contains two active sites with the consensus sequence ([DS]xxxExxNx(22)P), with four conserved residues thought to form the phosphatase active site. The C-terminal helix of CheC acts as a mimic of the natural enzymatic target of CheD, the alpha-helical receptors, and serves as the binding site for CheD. The CheC/CheD heterodimerization increases CheY-P phosphatase activity five-fold. Class I CheCs are involved in adaptation of the chemotaxis system.	8.02942e-65
NZ_CP014150.1\|WP_101509064.1\|2613636_2615361_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	4.86714e-165
NZ_CP014150.1\|WP_057547754.1\|2621193_2622267_-\|chemotaxis-response-regulator-protein-glutamate-methylesterase	gnl\|CDD\|234828	PRK00742, PRK00742, chemotaxis-specific protein-glutamate methyltransferase CheB.	4.39751e-147
NZ_CP014150.1\|WP_021128122.1\|2618394_2618748_-\|response-regulator	gnl\|CDD\|381097	cd17542, REC_CheY, phosphoacceptor receiver (REC) domain of chemotaxis protein CheY. The chemotaxis response regulator CheY contains a stand-alone REC domain. Chemotaxis is a behavior known for motile bacteria that directs their movement in response to chemical gradients. CheY is involved in transmitting sensory signals from chemoreceptors to the flagellar motors. Phosphorylated CheY interacts with the flagella switch components FliM and FliY, which causes counterclockwise rotation of the flagella, resulting in smooth swimming. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.15328e-51

>NZ_CP014150.1|WP_057547754.1|2621193_2622267_-|chemotaxis-response-regulator-protein-glutamate-methylesterase
MESNKKIKVLVVDDSSMFRRIIKNYLQENPDLEVVDTAKDPYEARDKILQLRPDVLTLDIEMPGMNGIDFLKILMDQCPIPTIVISGADGRCFEAISAGAVGFVEKPTANTMKDFSIDLASKIREASVAKLEKSITKTNTSKIINKGNILNHIGIRKNNSKEIIAIGASMGGVEAVGKLLKQLPLGLPGIVVTQHMPPVFTQRYAERLNKECLINVSEGKDGEEVLSGHAYIAPGGFQMGIIKKNNKYVLEIIEGEKVSGHCPSVDYLFQSVAKVAKDNSIGVILTGMGSDGAKGLLDIKESGGYTIGQNRQSCVVYGMPMAAKNIGAVAKETSLEMIPNSILNQLKRRQSTVKSND
>NZ_CP014150.1|WP_021128126.1|2620561_2621176_-|chemotaxis-protein-CheC
MKFECDKLNVFREISNIGSGNASSSLAIMLNELVDIGIPKSDMIKFSDITNSYSSPEELVVGTVLQLSGDMEGFIMVIMKVDSAFNLLSRISGKEITCDKNDYNAVCEELSSIGEICNILCGTYLTAISDMTNLSITPSIPYFSVDMVMAIMNLPMSLYGPVSDSILCIETEFFTADRSIDGKYYFIPKVESCNKLLSSLGFAD
>NZ_CP014150.1|WP_021128125.1|2620064_2620550_-|chemotaxis-protein-CheD
MEKITVGIADFNIVKAPDRISTIGLGSCCGVVIYDEVNKIAGLVHILLAESKYDKKLVNKAKYADTGITLLYEEMKKAGANTRFMRAKIAGGAHMFSFKNTTNSIFTIGEKNVKACKETLAKLRVMIVSEDVLGSCGRTIVFDTNTNKLLIKSVGKSEKFI
>NZ_CP014150.1|WP_021128124.1|2619564_2620047_-|purine-binding-chemotaxis-protein-CheW
MEANEEIIENKIDDLYMVFIINNQKYALSSKYIIEIIEMLPITKVPFLPNYMKGIINLRSTIIPVMDARMRFDMEPIAYNERTCIIIIENDSNKIGLIVDAVNEVINISPTQSMNMNSNNDESKENFIKGVSEINDEVQLILDCDSLMKIVEDIKNEINE
>NZ_CP014150.1|WP_038293377.1|2618771_2619581_-|protein-glutamate-O-methyltransferase-CheR
MKLTNKDFVRLKTFMYNNYGINLENKRTLIETRLVLMVKRLGFEDFKSYIDSLMLDKTGDQAAILVEKLTTNFTYFMREEQHFEFLRNEVLLPHFKKPRVGGLKIWSAASSTGEEPYCIAMLASSVFGRNTKLKVSISASDISNNVLKQAKSGVYSQDKIDKLPQAWVKNFFQQIDNRNYAICDSIKSLVDFKYFNLNNSIGWERNKYDVIFCRNVMIYFDNPTKQNLSKRLYDALKPGGYLIIGMSENLSNLKTDFERVKPSVYRKMI
>NZ_CP014150.1|WP_021128122.1|2618394_2618748_-|response-regulator
MKRVLIVDDAAFMRMSIRKMLEENGFEIVGEAENGLMAIEKYQELQPEVVTMDITMPEMDGLEALRQIKKIDPAASIVMVSALGQEARMKEAIIYGAKGFIVKPFKEEIIVSALAKL
>NZ_CP014150.1|WP_021128121.1|2617213_2618101_-|FliM/FliN-family-flagellar-motor-switch-protein
MKQKVTVYDFKKPQRYSTGNMRFLSVIAEEFCKSINLFVTYELKRPNIVCKLDRIEQTNYEEFMNMISNDSVIVEHAIQPLVKGLIYQLDKSVALTFIDLILGGDGEFGDTKRELTAVDRELISYVGSKFLTKMYIFEGCENREVSHIYTNVGSSKKYPISESVVISHMKMMDGDKEVGRMSFCNPYSCMEPVLEQLEPKRLFKSKSIEYDFEFTNAIYNKICGTSTDMVAILGRTKVSVEELLDLKVGDVITLDTKVDGDMDLHVGGSSAFKCKLGLIKNKKGVMITDCVKKEG
>NZ_CP014150.1|WP_021128120.1|2616945_2617209_-|FliM/FliN-family-flagellar-motor-switch-protein
MSEKFDRVLDIELKVSAILGRTQIALKDIFELSKGSLIELDTFEDQEVEITVNGRMIGYGQVVIVDDSFGVRITRILGEEELAKTLA
>NZ_CP014150.1|WP_021128119.1|2615597_2616866_+|DUF1002-domain-containing-protein
MSIKKKIISIVICSTMVLGSISLVFADSSKVVTLGANLTPEQKQTMLKYFGVNKNDAVILDVNNQEERKYLEGIAPESQIGTKTYSCAYVEPTKSGSGINVKTANITWVTSSMIASTLASLGITDANCVIAANFPVSGTGALTGVMKAYEDATGKPLDEKKKEIATEELVVTGDLGQDVGKDKATGIINDIKTQVIKNNTSDTVQIADTINNITNNYNVTLSPEQQKQIENLMLKISKQDYNYKEMKDALESVSNTVNDHLKELGENVNNSGILDTVKGWFDGIGNWVSNLFGGDNKDLGILENTNDKLLGDNAKIDATDKNAINLPSNEEVEGFFTKVWNWFTGLFNNEPKKEESTDNSNSQSENTNNESNNNEINDNENATKSEQSSDLENKDNNANHNNDVNNINDANSQIDNNTQKSN
>NZ_CP014150.1|WP_101509064.1|2613636_2615361_-|ABC-transporter-ATP-binding-protein
MLKLLKNLKKYKWVVVIIFLLVFIQALCDVYLPNLMSNIVDIGIINNDKAYILKIGFIMLGVSLIGVIATILASYFGAKVAMGFGRDIREKVFEQVETFSLKEVNDLGVSSLITRTTNDVTQIQQVLIIMLRMMLYAPMVAIGATIMAIRKDSKLSLIILVSIPILILSIYLIASKAIPLFKKMQKNVDKLNRVLRENLTGIRVIRVFNKYKLEKQKFEKSSFQLSDIAIKANRTITLLMPIMMLLVNLSIIAVVWFGGIRIDKGNMQVGDLIAFIQYLTQIMFALMMLSMMFVMVPRASASADRINEILGKKSEIYSKEKAIKETEKTGYLEFKNVSFYYDENSEKVLDNINFTSGPGETTAIIGGTGSGKSTLIKLIPRLLEVNEGEVLVDGINVKDMDLKVLRDKIGYVPQKSVLFTGTIKENIVYGDDDASNDDIKSAIDISQSKEFINEKKDRENSYIAQGGNNVSGGQKQRLAIARAIVKKPEIYIFDDSFSALDFKTDKNLREALKEETKKSTVIIVAQRVSTVINADRIIVLDEGKVIKIGTHKELLETCDIYKEIVYSQLSKEEI
>NZ_CP014150.1|WP_021128129.1|2624676_2626413_-|HAMP-domain-containing-protein
MKNLKIGRKLSIAFIVLLMITTFANFYTISKLRQAEDLSSILFNRPYKQTNDSMEIRRDLVSIGREISNAILRENPGKYKAGIESDFNSIYEKVEKISKSFGGDKNLVDSIKSTTQNLQNQYNNVFAVLESGDYKKAKEITDDNTEYRNAYEQSVEAAVTFNKEADKRGNLFNDEIQDASSRAIFASTAISIVSIGIGAVICIFMTKSLKKPIEDIEKAANKMAEGDFDIEIDYESKDELGSLSNSMKQMSNTTKDVINDTVRVLGEVALGNFNVEPEAKYIGVFKDIEKSVVRITNDLSETMSQINLAAEEVGAASDQVAGGSQMLSQGATEQASAIQELSATLTEISEKIQDTAQNAKKANSLTLSSGRDVKEGNEQMKQMVKAMEEISFTSSEIGRIIKTIDDIAFQTNILALNAAVEAARAGEAGKGFAVVADEVRNLAAKSAEAAKNTATLIENSIEAVGKGTEIVDNTAQSLQKIINTTNKTISVVDEIAKASDEEANAINQVTLGVEQISEVVQTNSATSEESAAASEELSGQAQMLKSLIENFKLKNINDSRKSIDFNNDKVNFVGNELD
>NZ_CP014150.1|WP_055328261.1|2626820_2627426_-|hypothetical-protein
MKFSKLVSLGLIGLLTFGTVGCTTKTEEKKATEKAKTETTTEARDNMTLESYKTEFGKLYDTNIARLENYSKYKDIAVEEPTKDYPGNEAYLNELKKSYKDSEVKLQEFVNSLKKVKTDDPKLKEMNDKLIKEGDKVIGELKARSKKLEEVPNDLMSKSEVEFRRGLNDLVKVDNTAKSDFEKMINDVNEFLGMKPSNTKK
>NZ_CP014150.1|WP_021128131.1|2627743_2629678_-|iron-hydrogenase-small-subunit
MDNNKPTIIQSSLGSVFSVFSESELKELTDDNSRKIAIAGKVNNPGIIEIPEKATLREIIDLAGGIIKKREFKAAQLGIPFGGFLTEDSLDKELDFSLFGKDSGRSIIILSQEDCIVQYAKFYIDFLIGKMKEDKYKKYEKVKDEIIQMWKILDRISKGRSNMRDVFILRELASTVKTTLNQNHNIMQEIIDKFYEEIEEHIEDEKCYTAQCNNLVKLTITGKCIGCGACKRVCPVDCISGERKEQHYIDYNRCTHCGQCIASCPVDAITAGDNTLKFLRDLATPNKVVITQMAPAIRVAIGEAFGFEPGENVEKKIAAALRKLGVDYVFDTTWAADLTIMEEAAELQERLEKHLNGDKDVKLPILTSCCPAWVKFIEQNYGDMLDVPSSAKSPMQMFATVAKDLWGREKGLTRDQITSVAIMPCIAKKYEASRKEFSRGLNYDVDYVITTRELIKIFEDSGINLKEIEDEEIDQVLGEYTGAGIIFGRTGGVIEAATRTAIENMTGEKIENVEFEALRGWDSFRSCDLEVSGMKLRIGVAYGLKEAGKMLDKIRAGEEFYHAIEIMACLGGCVGGGGQPKARKRAETVEKRAEGLNNIDRSLTLRVSKENPAVQAIYDKYLGHPLSHRAHELLHTRYFVKVKK
>NZ_CP014150.1|WP_021128132.1|2629842_2630904_-|flavodoxin-dependent-(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase
MSYKRRLSKEVSVGSLKIGGNNPISIQSMTNTDTRDAKATIDQIKRLEEVGCDVVRVAVPDMEAAKNIGEIKKNVNIPIIADIHFDYRLALEAIDQGVDGVRINPGNIGSIDRVKMVVNKCREKNLKIRIGVNGGSLEKELLEKYGSATAEALVESAMGHVKILEDLDFHNIVISLKSSDIYKTLDAYELIAKKVDYPLHIGITESGSVKKGTIKSSIGVGALLLKGIGDTIRISLTGDPTEEVIVGKEILRSLDLLNDKIKVISCPTCGRCNIDLISVVNEVEEKINKVDKDITVAIMGCAVNGPGEAKEADIGIAGGKGEGLLFKKGEIIRKINGDKLVDELLAEIENYKK
>NZ_CP014150.1|WP_057562128.1|2630935_2631955_-|RIP-metalloprotease-RseP
MNILTILVAILAFGIIVFIHELGHFLFAKKAGVRIHEFAIGMGPKIYGFQKGETTYSIRLLPLGGYVAMEGEDSDSKDPRAFGNKSILQRASILFAGPFFNIILTVIILIPVFMYIGTPSTKLKSVIDNSAAQRAGIQAGDTITEVNGKDVKSWNELSKEIQDSNGNKLNITLERDGKEKKVNLIPESKDGKYLIGIYPKYEKSILGSFTTAIKTTISMIVGMITFLGQLITGNLPGGIDQSLAGPIGVISIVADATKTGIINVLYLAAVISLNLGVLNLLPIPALDGGRLFFLFIEFLRGGRKIDPNKEGMINVIGFAVLMVFMLFVTYKDIVRLMAS
>NZ_CP014150.1|WP_101509066.1|2631967_2633119_-|1-deoxy-D-xylulose-5-phosphate-reductoisomerase
MKKISILGSTGSIGTQTLDVVRKNRDKFEVVAISANSSINLLLEQIKEFKPKYVAVYNENRAKQLKEIIPRDIKIEVLSGMDGLVTISSLDEIDVLLTAIVGMIGLVPTLEAIKKGKTIALANKETLVTAGQLVMEEARKRNVDILPVDSEHSAIFQCLNGENKKEIDSIILTASGGPFRGKTKEELLNVTKNEALKHPNWSMGRKISIDSSTLMNKGLEVIEAKWLFDVDSEKIDVVVHPQSIIHSMVQFVDSSIIAQMGCPDMKLPIQYALTYPNRLLNDFERLDFSKLNGLTFEKPDLETFPCLQLAYESLKSGGTYSAVLNAANEVLVNEFLEDKIKFYDIPYYIEKTLEAHDSIKKPTLEEILHIDKWSRDFVKKCIK
>NZ_CP014150.1|WP_021128135.1|2633182_2633959_-|phosphatidate-cytidylyltransferase
MVVRIIAALALIPLLLFVIYGGLPLYIAEAIIGIIALDEFYKAFKSKSIQPISILGYVFAIYLSMRHVLNLNSEYTYILVFTLFLIGIIYMLTNKKNILDFSITFIGMFYIPIFLDFIVLTINNFDLGNIYVWLIFIVSFMTDTFAYFSGYLFGRHKLIPSISPKKTIEGSIGGILGSTICCVAFGYVFNLGIAHMILVGSIGSVVAQLGDLFASAIKRYVGIKDYGKLIPGHGGILDRFDSVILVAPFVYYAIYVFI
>NZ_CP014150.1|WP_021128136.1|2633971_2634706_-|isoprenyl-transferase
MNKKNKYDINLSNVPTHIAIIMDGNGRWAKERLLPRTVGHKAGVEAIRAVTKECSALGVKHLTLYAFSTENWKRPKLEVDALMNLLYTYLKKELKELHENNVKITTIGDIDVLPSKSMEAIKDAIDITKDNTGLNLNIALNYGSRNDIKNAVIDIVKKCKSGKIDIEDINEDTISKYLSTKSIPDPDLIIRTSGEQRISNFLLWEIAYSEFYFTDVYWPDFNSNELRKAIYTYQNRDRRFGGLK
>NZ_CP014150.1|WP_021124639.1|2634736_2634940_-|hypothetical-protein
MKKYYNLLGLHTDEVANFFEKENKNYTIKTIKGYKDTEKLIIPRVIKISEVENCVEIIQTYFADSLK
>NZ_CP014150.1|WP_021128137.1|2634942_2635500_-|ribosome-recycling-factor
MSAQVKKQLDEKMNKTIEALKKEFTTIRAGRANAQMLDKVRVDYYGTPTPVNQVGAISVPEPRTLMINPWDKTAMAEIEKAIRNSDLGLNPTNDGQVIRISVPALTEERRKDLAKQASKVAEEFKVRLRNERRDANDKLKKMEKEGEITEDDLKKSQDEVQKITDKFIKEVDSLLKAKEQDIMAV

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP014150_2	2.1\|1152430\|27\|NZ_CP014150\|CRISPRCasFinder	1152430-1152456	27	NC_022111	Prevotella sp. oral taxon 299 str. F0039 plasmid, complete sequence	1728908-1728934	5	0.815
NZ_CP014150_2	2.1\|1152430\|27\|NZ_CP014150\|CRISPRCasFinder	1152430-1152456	27	NZ_CP034228	Lactobacillus agilis strain La3 plasmid pLa3_3, complete sequence	1238-1264	5	0.815
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	MN693431	Marine virus AFVG_25M363, complete genome	5323-5356	7	0.794
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	NZ_KT897275	Clostridium botulinum strain IFR 12/29 plasmid p12/29, complete sequence	37504-37537	8	0.765
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	NZ_KT897276	Clostridium botulinum strain INGR16-02E1 plasmid pINGR16-02E1, complete sequence	37520-37553	9	0.735
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	NZ_KT897280	Clostridium botulinum strain FI1111E1 plasmid pFI1111E1, complete sequence	36433-36466	9	0.735
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	NZ_KT897277	Clostridium botulinum strain ST0210E1 plasmid pST0210E1, complete sequence	37520-37553	9	0.735
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	NZ_KT897278	Clostridium botulinum strain FWSKR40E1 plasmid pFWSKR40E1, complete sequence	36433-36466	9	0.735
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	NZ_KT897279	Clostridium botulinum strain SWKR38E2 plasmid pSWKR38E2, complete sequence	36433-36466	9	0.735
NZ_CP014150_5	5.1\|2623685\|34\|NZ_CP014150\|CRISPRCasFinder	2623685-2623718	34	MN693095	Marine virus AFVG_25M68, complete genome	15187-15220	9	0.735
NZ_CP014150_4	4.1\|1538377\|33\|NZ_CP014150\|CRISPRCasFinder	1538377-1538409	33	NZ_CP025986	Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence	1115904-1115936	10	0.697

1. spacer 2.1|1152430|27|NZ_CP014150|CRISPRCasFinder matches to NC_022111 (Prevotella sp. oral taxon 299 str. F0039 plasmid, complete sequence) position: , mismatch: 5, identity: 0.815

aaaaacatacagtgtgaagaatttaaa	CRISPR spacer
taaaacaaacagtatgaagaatttatt	Protospacer
 ****** *****.***********

2. spacer 2.1|1152430|27|NZ_CP014150|CRISPRCasFinder matches to NZ_CP034228 (Lactobacillus agilis strain La3 plasmid pLa3_3, complete sequence) position: , mismatch: 5, identity: 0.815

aaaaacatacagtgtgaagaatttaaa	CRISPR spacer
tataacaaacagtctgaagaatttaag	Protospacer
 * **** ***** ************.

3. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to MN693431 (Marine virus AFVG_25M363, complete genome) position: , mismatch: 7, identity: 0.794

caactttagtttcttttacttctatattatcggc	CRISPR spacer
caataatcgcttcttttaattttatattatcggc	Protospacer
***.  * *.******** **.************

4. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to NZ_KT897275 (Clostridium botulinum strain IFR 12/29 plasmid p12/29, complete sequence) position: , mismatch: 8, identity: 0.765

caactttagtttcttttacttctatattatcggc	CRISPR spacer
gtactttagtttcttttacttctattttaaaatt	Protospacer
  *********************** ***  . .

5. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to NZ_KT897276 (Clostridium botulinum strain INGR16-02E1 plasmid pINGR16-02E1, complete sequence) position: , mismatch: 9, identity: 0.735

caactttagtttcttttacttctatattatcggc	CRISPR spacer
gtactttagtttcttttacttctaatttaaaatt	Protospacer
  **********************  ***  . .

6. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to NZ_KT897280 (Clostridium botulinum strain FI1111E1 plasmid pFI1111E1, complete sequence) position: , mismatch: 9, identity: 0.735

caactttagtttcttttacttctatattatcggc	CRISPR spacer
gtactttagtttcttttacttctaatttaaaatt	Protospacer
  **********************  ***  . .

7. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to NZ_KT897277 (Clostridium botulinum strain ST0210E1 plasmid pST0210E1, complete sequence) position: , mismatch: 9, identity: 0.735

caactttagtttcttttacttctatattatcggc	CRISPR spacer
gtactttagtttcttttacttctaatttaaaatt	Protospacer
  **********************  ***  . .

8. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to NZ_KT897278 (Clostridium botulinum strain FWSKR40E1 plasmid pFWSKR40E1, complete sequence) position: , mismatch: 9, identity: 0.735

caactttagtttcttttacttctatattatcggc	CRISPR spacer
gtactttagtttcttttacttctaatttaaaatt	Protospacer
  **********************  ***  . .

9. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to NZ_KT897279 (Clostridium botulinum strain SWKR38E2 plasmid pSWKR38E2, complete sequence) position: , mismatch: 9, identity: 0.735

caactttagtttcttttacttctatattatcggc	CRISPR spacer
gtactttagtttcttttacttctaatttaaaatt	Protospacer
  **********************  ***  . .

10. spacer 5.1|2623685|34|NZ_CP014150|CRISPRCasFinder matches to MN693095 (Marine virus AFVG_25M68, complete genome) position: , mismatch: 9, identity: 0.735

caactttagtttcttttacttctatattatcggc	CRISPR spacer
cttctttcgtttcttttacttctttatcagccat	Protospacer
*  **** *************** ***.* * ..

11. spacer 4.1|1538377|33|NZ_CP014150|CRISPRCasFinder matches to NZ_CP025986 (Ralstonia solanacearum strain RSCM plasmid p-unname2, complete sequence) position: , mismatch: 10, identity: 0.697

gccagcaactgatccaaatcagccaacgccacc	CRISPR spacer
aagcggggctgatccagatccgccaacgccacg	Protospacer
.   * ..********.*** ***********

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

730599 : 737220

Acanthamoeba_polyphaga_mimivirus(16.67%)

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_055332423.1\|730599_731538_+	SPFH/Band 7/PHB domain protein	A0A0G2YDT0	Acanthamoeba_polyphaga_mimivirus	3.9e-20	34.4
WP_101508232.1\|731689_732595_+	S8 family peptidase	A0A127AWU5	Bacillus_phage	1.3e-57	44.0
WP_054632000.1\|732709_733396_+	cell division ATP-binding protein FtsE	G9BWD6	Planktothrix_phage	1.3e-28	36.1
WP_057541742.1\|733379_734279_+	ABC transporter permease	NA	NA	NA	NA
WP_101508234.1\|734299_735391_+	peptidoglycan DD-metalloendopeptidase family protein	A0A292GJG6	Xanthomonas_phage	1.6e-25	50.0
WP_038293741.1\|735486_735990_+	3'-5' exonuclease	A0A0A7RWA3	Clostridium_phage	3.5e-20	38.8
WP_054632003.1\|736158_737220_+	serine/threonine protein kinase	D2X3B9	Enterobacteria_phage	2.2e-48	36.2

DBSCAN-SWA_2

1160733 : 1167274

Thermus_phage(28.57%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_055329278.1\|1160733_1161192_-	ImmA/IrrE family metallo-endopeptidase	S6B1N5	Thermus_phage	1.4e-20	44.6
WP_021128549.1\|1161210_1161612_-	helix-turn-helix transcriptional regulator	A8ATJ9	Listeria_phage	1.1e-16	40.2
WP_101508413.1\|1161779_1161998_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_101508414.1\|1162015_1162828_+	phage antirepressor KilAC domain-containing protein	A0A2H4PQV4	Staphylococcus_phage	7.4e-52	42.0
WP_101508415.1\|1162862_1163855_+	YqaJ viral recombinase family protein	S6C475	Thermus_phage	9.3e-57	39.3
WP_158645324.1\|1164441_1164609_+	hypothetical protein	NA	NA	NA	NA
WP_158645325.1\|1164852_1165596_+	recombinase RecT	Q0H279	Geobacillus_phage	3.2e-46	42.1
WP_101508418.1\|1165722_1166610_+	DnaD domain protein	A6M985	Geobacillus_virus	2.0e-58	54.4
WP_101508419.1\|1166521_1167274_+	ATP-binding protein	A6XMI1	Bacillus_virus	2.5e-38	39.8

DBSCAN-SWA_3

1380413 : 1391343

Pandoravirus(25.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_055329122.1\|1380413_1381373_+	peptidase	U5Q1E2	Bacillus_phage	1.7e-18	46.8
WP_101508502.1\|1381382_1382093_+	polysaccharide deacetylase family protein	NA	NA	NA	NA
WP_054630795.1\|1382177_1382501_+	hypothetical protein	A0A0A8WF25	Clostridium_phage	1.9e-27	61.1
WP_155484440.1\|1382514_1382676_-	hypothetical protein	NA	NA	NA	NA
WP_055333956.1\|1382896_1383490_+	aminodeoxychorismate/anthranilate synthase component II	A0A0P0IKJ1	Acinetobacter_phage	9.5e-57	53.9
WP_101508503.1\|1383483_1384824_+	aminodeoxychorismate synthase component I	S4VNU7	Pandoravirus	3.8e-37	38.5
WP_101509405.1\|1384816_1385563_+	aminotransferase class IV	NA	NA	NA	NA
WP_057557868.1\|1385541_1386225_+	hypothetical protein	NA	NA	NA	NA
WP_057541524.1\|1386260_1386833_+	GTP cyclohydrolase I FolE	E7DN69	Pneumococcus_phage	3.3e-46	53.4
WP_054630800.1\|1386843_1387635_+	dihydropteroate synthase	A0A0B5J4J5	Pandoravirus	9.8e-25	28.2
WP_101508504.1\|1387642_1388008_+	dihydroneopterin aldolase	NA	NA	NA	NA
WP_057546219.1\|1388000_1388507_+	2-amino-4-hydroxy-6- hydroxymethyldihydropteridine diphosphokinase	NA	NA	NA	NA
WP_101508505.1\|1388487_1389267_+	3-deoxy-7-phosphoheptulonate synthase	E3T537	Cafeteria_roenbergensis_virus	3.9e-18	30.1
WP_101508506.1\|1389525_1391343_+	DNA primase	A0A0K1LMQ9	Caulobacter_phage	1.0e-53	34.2

DBSCAN-SWA_4

1416049 : 1424633

Bacillus_phage(66.67%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_101508519.1\|1416049_1418254_+	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	9.0e-44	29.8
WP_057543718.1\|1418285_1420106_+	ABC transporter ATP-binding protein	W8CYL7	Bacillus_phage	3.2e-47	30.3
WP_021124043.1\|1420211_1420415_+	cold-shock protein	Q9AZD3	Lactococcus_phage	5.9e-19	68.2
WP_057564165.1\|1420628_1422467_+	asparagine synthase (glutamine-hydrolyzing)	A0A1V0SGM7	Hokovirus	8.1e-38	32.3
WP_038293467.1\|1422480_1423176_+	response regulator transcription factor	W8CYM9	Bacillus_phage	1.0e-38	37.7
WP_055329097.1\|1423178_1424633_+	HAMP domain-containing histidine kinase	W8CYF6	Bacillus_phage	4.7e-25	26.2

DBSCAN-SWA_5

1437635 : 1516313

Clostridium_phage(61.67%)

integrase,coat,tail,holin,protease,capsid,head,portal,terminase

attL 1436817:1436834|attR 1502489:1502506

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
1436817:1436834	attL	NA	NA	NA	NA
WP_101508527.1\|1437635_1438112_-	hypothetical protein	B6SBW7	Clostridium_virus	9.9e-49	61.8
WP_101509408.1\|1438128_1438587_-	helix-turn-helix transcriptional regulator	A0A1Q1PVT4	Staphylococcus_phage	5.7e-17	69.2
WP_101509409.1\|1438744_1438960_+	DUF739 family protein	E8ZDN3	Streptococcus_phage	1.4e-05	32.4
WP_101508528.1\|1438985_1439732_+	ORF6C domain-containing protein	A0A0A8WJ22	Clostridium_phage	4.7e-21	60.9
WP_021128284.1\|1439845_1440049_+	hypothetical protein	NA	NA	NA	NA
WP_101508529.1\|1440116_1440380_+	hypothetical protein	NA	NA	NA	NA
WP_101508530.1\|1440460_1441444_+	YqaJ viral recombinase family protein	Q0H280	Geobacillus_phage	2.0e-59	41.7
WP_101508531.1\|1441468_1442287_+	recombination protein RecT	S6AVW6	Thermus_phage	4.5e-57	48.8
WP_101508532.1\|1442362_1443223_+	replication protein	A0A0A8WI94	Clostridium_phage	3.0e-67	53.8
WP_101508533.1\|1443234_1443591_+	hypothetical protein	NA	NA	NA	NA
WP_101508534.1\|1443593_1444109_+	dUTP diphosphatase	NA	NA	NA	NA
WP_101508535.1\|1444113_1444308_+	hypothetical protein	NA	NA	NA	NA
WP_101508536.1\|1444384_1444786_+	RusA family crossover junction endodeoxyribonuclease	J9QE82	Clostridium_phage	2.9e-33	47.6
WP_021128275.1\|1444879_1445137_+	AbrB/MazE/SpoVT family DNA-binding domain-containing protein	A0A0K2CZ86	Paenibacillus_phage	1.1e-09	44.7
WP_021128274.1\|1445160_1445664_+	hypothetical protein	A0A090EUN5	Clostridium_phage	4.3e-42	58.3
WP_101508537.1\|1446126_1446813_+	SLATT domain-containing protein	NA	NA	NA	NA
WP_158645331.1\|1447017_1447194_+	hypothetical protein	NA	NA	NA	NA
WP_101508538.1\|1447258_1447948_+	helix-turn-helix domain-containing protein	A0A0A8WFS6	Clostridium_phage	1.9e-80	70.9
WP_101508539.1\|1447937_1449275_+\|terminase	PBSX family phage terminase large subunit	A0A1J1J8Z1	Escherichia_phage	1.7e-175	68.2
WP_101508540.1\|1449552_1450974_+\|portal	phage portal protein	A0A0A8WE96	Clostridium_phage	1.6e-142	54.1
WP_101508541.1\|1450975_1452673_+\|capsid	phage minor capsid protein	A0A1J1J8Z3	Escherichia_phage	1.3e-106	50.2
WP_057541491.1\|1452675_1452897_+	hypothetical protein	NA	NA	NA	NA
WP_101508542.1\|1452967_1453573_+	phage scaffolding protein	A0A0A7RW68	Clostridium_phage	7.0e-07	25.8
WP_101508543.1\|1453611_1454694_+\|coat	phage coat protein	A0A0A7RTH8	Clostridium_phage	1.9e-124	63.0
WP_101508544.1\|1454698_1455040_+	hypothetical protein	F6K8R2	Clostridium_phage	6.3e-13	42.1
WP_101508545.1\|1455042_1455468_+	hypothetical protein	F6K8R3	Clostridium_phage	2.5e-27	44.6
WP_101508546.1\|1455467_1455827_+\|capsid	capsid protein	F6K8R4	Clostridium_phage	1.7e-21	51.9
WP_057566563.1\|1455827_1456256_+	chloramphenicol resistance protein	A0A1J1J8Y6	Escherichia_phage	5.8e-40	58.2
WP_055329062.1\|1456261_1456747_+	hypothetical protein	F6K8R6	Clostridium_phage	2.0e-28	46.4
WP_101509410.1\|1456767_1457166_+	hypothetical protein	F6K8R7	Clostridium_phage	1.0e-06	34.3
WP_055329061.1\|1457165_1457786_+	bacteriophage Gp15 family protein	F6K8R8	Clostridium_phage	2.4e-50	55.8
WP_101508547.1\|1457838_1460730_+	tape measure protein	A0A1J1J8L9	Escherichia_phage	2.2e-13	34.6
WP_158645332.1\|1460753_1461476_+	hypothetical protein	NA	NA	NA	NA
WP_101508549.1\|1461487_1464079_+\|tail	phage tail protein	B6CXF5	Clostridium_phage	1.4e-115	43.1
WP_158645333.1\|1464014_1466747_+	hypothetical protein	B6CXE5	Clostridium_phage	4.2e-06	25.5
WP_101508551.1\|1466758_1467259_+	hypothetical protein	NA	NA	NA	NA
WP_101508552.1\|1467261_1467447_+	XkdX family protein	NA	NA	NA	NA
WP_057536086.1\|1467498_1467732_+	hemolysin XhlA family protein	Q0SPG4	Clostridium_phage	8.3e-17	55.8
WP_021128251.1\|1467748_1468000_+\|holin	phage holin family protein	A0A2H4J047	uncultured_Caudovirales_phage	2.8e-18	59.0
WP_101508553.1\|1468106_1469048_+	N-acetylmuramoyl-L-alanine amidase	A0A0N9SGH1	Paenibacillus_phage	6.0e-29	46.7
WP_101508554.1\|1469094_1469649_-	hypothetical protein	NA	NA	NA	NA
WP_101508555.1\|1470298_1470895_-	hypothetical protein	NA	NA	NA	NA
WP_101508556.1\|1470875_1471367_-	SocA family protein	A0A0N9SGM1	Paenibacillus_phage	1.4e-21	44.2
WP_101508557.1\|1471662_1471851_-	hypothetical protein	A0A0A8WFY8	Clostridium_phage	7.9e-18	74.6
WP_101508558.1\|1472710_1473166_-	hypothetical protein	NA	NA	NA	NA
WP_101508559.1\|1473611_1474160_-	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_057559634.1\|1474340_1475153_+	nitroreductase family protein	NA	NA	NA	NA
WP_054630939.1\|1475220_1476024_-	ABC transporter permease	NA	NA	NA	NA
WP_155484067.1\|1476010_1476184_-	hypothetical protein	NA	NA	NA	NA
WP_055329043.1\|1476216_1477809_-	recombinase family protein	A0A1L2BY67	Clostridium_phage	2.1e-111	44.5
WP_055330016.1\|1477864_1478308_-	ImmA/IrrE family metallo-endopeptidase	A8ATJ8	Listeria_phage	3.0e-15	35.3
WP_101508560.1\|1478330_1478762_-	helix-turn-helix transcriptional regulator	A0A0A8WFJ2	Clostridium_phage	7.9e-21	50.4
WP_101508561.1\|1478903_1479119_+	helix-turn-helix transcriptional regulator	S5MNF4	Brevibacillus_phage	1.0e-08	51.6
WP_055329040.1\|1479134_1479674_+	hypothetical protein	A0A0A7RW33	Clostridium_phage	1.5e-32	48.6
WP_055329039.1\|1479731_1479983_+	hypothetical protein	NA	NA	NA	NA
WP_101508562.1\|1480297_1480966_+	hypothetical protein	Q8SBM0	Clostridium_phage	9.5e-05	35.6
WP_101508563.1\|1481185_1481641_-	hypothetical protein	NA	NA	NA	NA
WP_101508564.1\|1481748_1482264_+	hypothetical protein	NA	NA	NA	NA
WP_101508565.1\|1482276_1482498_+	hypothetical protein	NA	NA	NA	NA
WP_054630932.1\|1483021_1483279_+	AbrB/MazE/SpoVT family DNA-binding domain-containing protein	A0A0K2CZ86	Paenibacillus_phage	3.7e-10	45.6
WP_101508566.1\|1483303_1483807_+	hypothetical protein	A0A0A8WIL5	Clostridium_phage	3.1e-40	57.1
WP_101508567.1\|1484258_1484459_+	hypothetical protein	NA	NA	NA	NA
WP_101508568.1\|1484554_1485103_+\|integrase	site-specific integrase	E2ELN7	Clostridium_phage	7.6e-61	61.0
WP_101508569.1\|1485369_1486050_+	manganese catalase family protein	NA	NA	NA	NA
WP_057538067.1\|1486199_1486613_+	hypothetical protein	NA	NA	NA	NA
WP_057570204.1\|1487294_1487756_+\|terminase	phage terminase small subunit P27 family	A0A0A7S0C4	Clostridium_phage	3.3e-33	51.0
WP_101508570.1\|1487769_1489491_+\|terminase	terminase large subunit	A0A0A7RVS5	Clostridium_phage	1.9e-227	66.7
WP_101508571.1\|1489506_1490769_+\|portal	phage portal protein	A6M949	Geobacillus_virus	2.8e-138	56.9
WP_101508572.1\|1490761_1491607_+\|protease	Clp protease ClpP	A0A0A7RTN2	Clostridium_phage	2.1e-73	59.1
WP_101508573.1\|1491659_1492814_+\|capsid	phage major capsid protein	A6M951	Geobacillus_virus	3.5e-79	47.9
WP_101508574.1\|1492958_1493234_+\|head,tail	phage gp6-like head-tail connector protein	A0A0A7RWM0	Clostridium_phage	5.6e-20	52.8
WP_101508575.1\|1493234_1493582_+\|head	phage head closure protein	Q0SPK6	Clostridium_phage	1.5e-30	59.3
WP_101508576.1\|1494496_1494859_+	hypothetical protein	Q0SPK8	Clostridium_phage	8.7e-29	54.2
WP_057567412.1\|1494893_1495247_+	hypothetical protein	A0A0A7S158	Clostridium_phage	3.6e-27	53.4
WP_101508577.1\|1495291_1495900_+	hypothetical protein	Q0SPK9	Clostridium_phage	4.9e-85	78.2
WP_101508578.1\|1495925_1496291_+	RNA polymerase subunit sigma	NA	NA	NA	NA
WP_101508579.1\|1496524_1497706_+\|tail	phage tail tape measure protein	Q0SPL2	Clostridium_phage	6.5e-73	83.6
WP_101508580.1\|1498927_1501312_+\|tail	phage tail tape measure protein	Q0SPL2	Clostridium_phage	3.0e-85	73.2
WP_101508581.1\|1501315_1502020_+	hypothetical protein	Q0SPL3	Clostridium_phage	2.0e-69	57.7
WP_101508582.1\|1502034_1502265_+	hypothetical protein	A0A0P0I3K6	Lactobacillus_phage	3.1e-08	38.7
WP_081012931.1\|1502293_1502689_+	hypothetical protein	M9Q2L1	Clostridium_phage	4.1e-24	47.7
1502489:1502506	attR	NA	NA	NA	NA
WP_158645334.1\|1502728_1506523_+\|tail	phage tail protein	H7BVF2	unidentified_phage	1.3e-74	47.3
WP_158645335.1\|1506523_1506682_+	hypothetical protein	NA	NA	NA	NA
WP_158645336.1\|1506810_1507020_+	hypothetical protein	NA	NA	NA	NA
WP_101508585.1\|1507080_1507377_+	hypothetical protein	A0A2H4J1Q4	uncultured_Caudovirales_phage	1.1e-24	56.5
WP_101508586.1\|1507357_1507585_+\|holin	phage holin	NA	NA	NA	NA
WP_101508587.1\|1507739_1508618_+	N-acetylmuramoyl-L-alanine amidase	A0A1L6BY22	Clostridium_phage	1.5e-21	40.4
WP_057559607.1\|1509494_1510313_+	PH domain-containing protein	A0A0F6N4L7	Staphylococcus_phage	9.4e-31	44.7
WP_101508588.1\|1511713_1511947_+	(2Fe-2S)-binding protein	NA	NA	NA	NA
WP_101508589.1\|1512131_1512596_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_101508590.1\|1512806_1513001_-	hypothetical protein	NA	NA	NA	NA
WP_101508591.1\|1513376_1514360_-	linear amide C-N hydrolase	M1I458	Paramecium_bursaria_Chlorella_virus	4.0e-20	32.7
WP_101508592.1\|1515064_1515565_+	hypothetical protein	NA	NA	NA	NA
WP_057558095.1\|1516079_1516313_+\|coat	spore coat associated protein CotJA	NA	NA	NA	NA

DBSCAN-SWA_6

3349739 : 3363505

Prochlorococcus_phage(25.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_101509325.1\|3349739_3353558_-	phosphoribosylformylglycinamidine synthase	A6N228	Microbacterium_phage	2.3e-34	23.9
WP_101509326.1\|3353616_3354870_-	phosphoribosylamine--glycine ligase	NA	NA	NA	NA
WP_101509327.1\|3354881_3356414_-	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	Q58MG4	Prochlorococcus_phage	3.4e-58	41.2
WP_021127483.1\|3356406_3357000_-	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	4.7e-24	38.4
WP_101509328.1\|3356993_3358022_-	phosphoribosylformylglycinamidine cyclo-ligase	Q58MH8	Prochlorococcus_phage	8.4e-69	45.2
WP_101509329.1\|3358015_3359386_-	amidophosphoribosyltransferase	A0A0M3SGR2	Mollivirus	5.6e-44	29.6
WP_055332839.1\|3359402_3360098_-	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0E3F9V5	Synechococcus_phage	2.8e-44	42.4
WP_101509330.1\|3360103_3360580_-	5-(carboxyamino)imidazole ribonucleotide mutase	A0A2P0VNU7	Tetraselmis_virus	2.4e-26	47.1
WP_101509331.1\|3360925_3361282_-	hypothetical protein	NA	NA	NA	NA
WP_021127477.1\|3361476_3362058_+	rubrerythrin family protein	NA	NA	NA	NA
WP_101509332.1\|3362170_3363505_-	NCS2 family permease	A0A0R6PHV4	Moraxella_phage	4.2e-52	32.0

Anti-CRISPR protein detection

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

2. NZ_CP014149

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

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

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

0 : 15057

Clostridium_phage(91.67%)

head,holin,tail

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_101508003.1\|848_1127_+\|head,tail	phage gp6-like head-tail connector protein	NA	NA	NA	NA
WP_101508004.1\|1110_1437_+\|head	phage head closure protein	I2E8V6	Clostridium_phage	8.1e-34	61.0
WP_101508040.1\|1448_1877_+	HK97 gp10 family phage protein	I2E8V7	Clostridium_phage	3.0e-52	65.5
WP_101508005.1\|1881_2235_+	hypothetical protein	Q8SBP4	Clostridium_phage	1.7e-37	66.4
WP_101508006.1\|2271_2877_+\|tail	phage tail protein	Q8SBP3	Clostridium_phage	6.9e-55	56.0
WP_057566211.1\|3057_3363_+	hypothetical protein	Q8SBP2	Clostridium_phage	1.8e-19	49.5
WP_101508007.1\|3440_3893_+	hypothetical protein	NA	NA	NA	NA
WP_101508008.1\|3927_6867_+\|tail	phage tail tape measure protein	Q8SBP1	Clostridium_phage	2.4e-100	47.1
WP_101508009.1\|6867_7578_+\|tail	phage tail family protein	Q8SBP0	Clostridium_phage	7.1e-59	48.9
WP_158645304.1\|7577_10133_+\|tail	phage tail protein	Q8SBN9	Clostridium_phage	3.8e-163	47.5
WP_101508011.1\|10119_12738_+	hypothetical protein	A0A0A8WHQ1	Clostridium_phage	1.2e-18	26.3
WP_101508012.1\|12749_13253_+	hypothetical protein	NA	NA	NA	NA
WP_101508013.1\|13245_13434_+	XkdX family protein	NA	NA	NA	NA
WP_101508014.1\|13488_13722_+	hemolysin XhlA family protein	Q0SPG4	Clostridium_phage	1.9e-16	54.5
WP_021121865.1\|13739_13958_+\|holin	phage holin	S4UAD2	Listeria_phage	1.4e-05	37.3
WP_101508015.1\|14112_15057_+	N-acetylmuramoyl-L-alanine amidase	A0A1L6BY22	Clostridium_phage	1.3e-23	38.9

DBSCAN-SWA_2

18854 : 33975

Clostridium_phage(28.57%)

terminase,protease,portal,integrase

attL 22838:22853|attR 28903:28918

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_101508021.1\|18854_19661_-	ParA family protein	A0A1V0DZZ0	Clostridioides_phage	4.2e-92	61.9
WP_101508022.1\|20011_21241_-	replication initiation protein	A0A218MNI2	uncultured_virus	1.1e-06	24.2
WP_101508023.1\|21687_22065_+	hypothetical protein	NA	NA	NA	NA
WP_101508024.1\|22209_22839_+	repressor LexA	A0A1B1P7Q3	Bacillus_phage	8.9e-13	50.7
22838:22853	attL	NA	NA	NA	NA
WP_101508025.1\|23013_23355_-	helix-turn-helix transcriptional regulator	E2ELL8	Clostridium_phage	4.5e-19	54.7
WP_158645305.1\|23528_23684_+	hypothetical protein	NA	NA	NA	NA
WP_101508026.1\|23695_24505_+	ORF6C domain-containing protein	A0A2H4JBC7	uncultured_Caudovirales_phage	3.5e-38	39.8
WP_101508027.1\|24498_24732_+	hypothetical protein	NA	NA	NA	NA
WP_101508041.1\|25038_25503_+	conserved phage C-terminal domain-containing protein	D2KRE4	Lactobacillus_phage	3.6e-19	51.4
WP_158645306.1\|25492_26185_+	ATP-binding protein	A6XMI1	Bacillus_virus	2.9e-25	33.9
WP_158645307.1\|26337_26496_+	hypothetical protein	NA	NA	NA	NA
WP_101508029.1\|26498_26897_+	hypothetical protein	NA	NA	NA	NA
WP_101508030.1\|26935_27187_+	hypothetical protein	NA	NA	NA	NA
WP_101508031.1\|27282_27795_+	hypothetical protein	A0A2H4J015	uncultured_Caudovirales_phage	8.9e-11	34.5
WP_101508032.1\|28006_28213_+	hypothetical protein	NA	NA	NA	NA
WP_101508033.1\|28231_28810_+\|integrase	site-specific integrase	E2ELN7	Clostridium_phage	1.7e-55	56.2
WP_101508034.1\|29001_29199_+	hypothetical protein	NA	NA	NA	NA
28903:28918	attR	NA	NA	NA	NA
WP_101508035.1\|29203_29620_+	HNH endonuclease	A0A0A7RUV1	Clostridium_phage	5.7e-24	45.6
WP_101508036.1\|29751_30237_+\|terminase	phage terminase small subunit P27 family	A6M947	Geobacillus_virus	1.5e-15	35.5
WP_101508037.1\|30238_31990_+\|terminase	terminase large subunit	A6M948	Geobacillus_virus	8.3e-125	42.2
WP_101508038.1\|31994_33281_+\|portal	phage portal protein	A6M949	Geobacillus_virus	1.4e-65	38.0
WP_101508039.1\|33249_33975_+\|protease	Clp protease ClpP	A0A0A8WFM9	Clostridium_phage	2.7e-74	61.4

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_CP014150

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection

2. NZ_CP014149

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection