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_CP019688	Corynebacterium glaucum strain DSM 30827 chromosome, complete genome	3 crisprs	csa3,cas4,DEDDh,cas3,WYL,DinG	0	0	2	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP019688_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019688_1

766709-766795

Orphan

Consensus_repeat	Method
ATGTCCCGACTCACCTGTCAAGCATCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019688_1

>merge|NZ_CP019688|1|766709-766795|CRISPRCasFinder
ATGTCCCGACTCACCTGTCAAGCATCACTCATCAAGTTAAGGTCGGCCTAAGTGTCAAGTATGTCTCGACTCACCTGTCAAGCATCA

>NZ_CP019688|1|1|766709-766795|CRISPRCasFinder
ATGTCCCGACTCACCTGTCAAGCATCA	CTCATCAAGTTAAGGTCGGCCTAAGTGTCAAGT
ATGTCTCGACTCACCTGTCAAGCATCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019688.1\|WP_095659538.1\|759474_760446_+\|UTP--glucose-1-phosphate-uridylyltransferase	unknown	unknown	gnl\|CDD\|224131
NZ_CP019688.1\|WP_095659545.1\|770089_771253_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|225371
NZ_CP019688.1\|WP_095659546.1\|772009_772453_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|181285
NZ_CP019688.1\|WP_095659536.1\|758137_758776_-\|SAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|212159
NZ_CP019688.1\|WP_095658980.1\|765270_766620_+\|IS256-family-transposase	unknown	unknown	gnl\|CDD\|307151
NZ_CP019688.1\|WP_157731254.1\|758810_759410_-\|5-formyltetrahydrofolate-cyclo-ligase	unknown	unknown	gnl\|CDD\|274270
NZ_CP019688.1\|WP_095659547.1\|772394_772985_-\|DNA-3-methyladenine-glycosylase-I	unknown	unknown	gnl\|CDD\|377025
NZ_CP019688.1\|WP_095659548.1\|773037_773448_+\|DoxX-family-protein	unknown	unknown	gnl\|CDD\|225168
NZ_CP019688.1\|WP_095659534.1\|757372_757936_+\|molybdenum-cofactor-biosynthesis-protein	unknown	unknown	gnl\|CDD\|238451
NZ_CP019688.1\|WP_095659535.1\|757940_758132_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019688.1\|WP_095659550.1\|774096_775761_-\|phospholipid-carrier-dependent-glycosyltransferase	unknown	unknown	gnl\|CDD\|224839
NZ_CP019688.1\|WP_095659541.1\|762547_763813_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|215641
NZ_CP019688.1\|WP_095659539.1\|760464_761754_+\|molybdopterin-molybdotransferase-MoeA	unknown	unknown	gnl\|CDD\|238452
NZ_CP019688.1\|WP_095661020.1\|771321_771924_-\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP019688.1\|WP_095659540.1\|761763_762423_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|224584
NZ_CP019688.1\|WP_095659542.1\|766859_767156_-\|metal-sensitive-transcriptional-regulator	unknown	unknown	gnl\|CDD\|376835
NZ_CP019688.1\|WP_095661019.1\|764054_765269_-\|IS481-family-transposase	unknown	unknown	gnl\|CDD\|366234
NZ_CP019688.1\|WP_095659549.1\|773422_774079_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227947
NZ_CP019688.1\|WP_095659544.1\|769396_770005_+\|cation-transporter	unknown	unknown	gnl\|CDD\|224151
NZ_CP019688.1\|WP_095659543.1\|767163_769287_-\|heavy-metal-translocating-P-type-ATPase	unknown	unknown	gnl\|CDD\|319850

Protein	Function_ID	Function_description	E-value
NZ_CP019688.1\|WP_095659538.1\|759474_760446_+\|UTP--glucose-1-phosphate-uridylyltransferase	gnl\|CDD\|224131	COG1210, GalU, UDP-glucose pyrophosphorylase [Cell envelope biogenesis, outer membrane].	8.58032e-121
NZ_CP019688.1\|WP_095659548.1\|773037_773448_+\|DoxX-family-protein	gnl\|CDD\|225168	COG2259, COG2259, Predicted membrane protein [Function unknown].	9.48969e-21
NZ_CP019688.1\|WP_095659546.1\|772009_772453_-\|hypothetical-protein	gnl\|CDD\|181285	PRK08199, PRK08199, thiamine pyrophosphate protein; Validated.	2.78605e-45
NZ_CP019688.1\|WP_095659536.1\|758137_758776_-\|SAF-domain-containing-protein	gnl\|CDD\|212159	cd11614, SAF_CpaB_FlgA_like, SAF domains of the flagella basal body P-ring formation protein FlgA and the flp pilus assembly CpaB. FlgA is a putative periplasmic chaperone that assists in the formation of the flagellar P ring; CpaB is a protein invoved in the assembly of the flp pili, which are bacterial virulence factors mediating non-specific adherence to surfaces; these proteins appear to contain a single SAF domain. This intermediate family also contains the SAF domains of sialic acid synthetases and type III antifreeze proteins, which also share the same extensive core structure.	4.65703e-09
NZ_CP019688.1\|WP_095658980.1\|765270_766620_+\|IS256-family-transposase	gnl\|CDD\|307151	pfam00872, Transposase_mut, Transposase, Mutator family.	1.31372e-127
NZ_CP019688.1\|WP_157731254.1\|758810_759410_-\|5-formyltetrahydrofolate-cyclo-ligase	gnl\|CDD\|274270	TIGR02727, Uncharacterized_protein_YqgN, 5,10-methenyltetrahydrofolate synthetase. This enzyme, 5,10-methenyltetrahydrofolate synthetase, is also called 5-formyltetrahydrofolate cycloligase. Function of bacterial proteins in this family was inferred originally from the known activity of eukaryotic homologs. Recently, activity was shown explicitly for the member from Mycoplasma pneumonia. Members of this family from alpha- and gamma-proteobacteria, designated ygfA, are often found in an operon with 6S structural RNA, and show a similar pattern of high expression during stationary phase. The function may be to deplete folate to slow 1-carbon biosynthetic metabolism. [Central intermediary metabolism, One-carbon metabolism].	3.44066e-35
NZ_CP019688.1\|WP_095659547.1\|772394_772985_-\|DNA-3-methyladenine-glycosylase-I	gnl\|CDD\|377025	pfam03352, Adenine_glyco, Methyladenine glycosylase. The DNA-3-methyladenine glycosylase I is constitutively expressed and is specific for the alkylated 3-methyladenine DNA.	4.40738e-93
NZ_CP019688.1\|WP_095659549.1\|773422_774079_+\|hypothetical-protein	gnl\|CDD\|227947	COG5660, COG5660, Predicted integral membrane protein [Function unknown].	9.95721e-21
NZ_CP019688.1\|WP_095659534.1\|757372_757936_+\|molybdenum-cofactor-biosynthesis-protein	gnl\|CDD\|238451	cd00886, MogA_MoaB, MogA_MoaB family. Members of this family are involved in biosynthesis of the molybdenum cofactor (MoCF) an essential cofactor of a diverse group of redox enzymes. MoCF biosynthesis is an evolutionarily conserved pathway present in eubacteria, archaea, and eukaryotes. MoCF contains a tricyclic pyranopterin, termed molybdopterin (MPT). MogA, together with MoeA, is responsible for the metal incorporation into MPT, the third step in MoCF biosynthesis. The plant homolog Cnx1 is a MoeA-MogA fusion protein. The mammalian homolog gephyrin is a MogA-MoeA fusion protein, that plays a critical role in postsynaptic anchoring of inhibitory glycine receptors and major GABAa receptor subtypes. In contrast, MoaB shows high similarity to MogA, but little is known about its physiological role. All well studied members of this family form highly stable trimers.	4.34618e-39
NZ_CP019688.1\|WP_095659543.1\|767163_769287_-\|heavy-metal-translocating-P-type-ATPase	gnl\|CDD\|319850	cd07552, P-type_ATPase_Cu-like, P-type heavy metal-transporting ATPase, similar to Archaeoglobus fulgidus CopB, a Cu(2+)-ATPase. Archaeoglobus fulgidus CopB transports Cu(2+) from the cytoplasm to the exterior of the cell using ATP as energy source, it transports preferentially Cu(2+) over Cu(+), it is activated by Cu(2+) with high affinity and partially by Cu(+) and Ag(+). This subclass of P-type ATPase is also referred to as CPx-type ATPases because their amino acid sequences contain a characteristic CPC or CPH motif associated with a stretch of hydrophobic amino acids and N-terminal ion-binding sequences. This subfamily belongs to the P-type ATPases, a large family of integral membrane transporters that are of critical importance in all kingdoms of life. They generate and maintain (electro-) chemical gradients across cellular membranes, by translocating cations, heavy metals and lipids, and are distinguished from other main classes of transport ATPases (F- , V- , and ABC- type) by the formation of a phosphorylated (P-) intermediate state in the catalytic cycle.	0
NZ_CP019688.1\|WP_095659550.1\|774096_775761_-\|phospholipid-carrier-dependent-glycosyltransferase	gnl\|CDD\|224839	COG1928, PMT1, Dolichyl-phosphate-mannose--protein O-mannosyl transferase [Posttranslational modification, protein turnover, chaperones].	2.6907e-38
NZ_CP019688.1\|WP_095659541.1\|762547_763813_+\|hypothetical-protein	gnl\|CDD\|215641	PLN03237, PLN03237, DNA topoisomerase 2; Provisional.	0.00266536
NZ_CP019688.1\|WP_095659539.1\|760464_761754_+\|molybdopterin-molybdotransferase-MoeA	gnl\|CDD\|238452	cd00887, MoeA, MoeA family. Members of this family are involved in biosynthesis of the molybdenum cofactor (MoCF), an essential cofactor of a diverse group of redox enzymes. MoCF biosynthesis is an evolutionarily conserved pathway present in eubacteria, archaea and eukaryotes. MoCF contains a tricyclic pyranopterin, termed molybdopterin (MPT). MoeA, together with MoaB, is responsible for the metal incorporation into MPT, the third step in MoCF biosynthesis. The plant homolog Cnx1 is a MoeA-MogA fusion protein. The mammalian homolog gephyrin is a MogA-MoeA fusion protein, that plays a critical role in postsynaptic anchoring of inhibitory glycine receptors and major GABAa receptor subtypes.	2.7565e-114
NZ_CP019688.1\|WP_095661020.1\|771321_771924_-\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	2.8699e-11
NZ_CP019688.1\|WP_095659540.1\|761763_762423_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|224584	COG1670, RimL, Acetyltransferases, including N-acetylases of ribosomal proteins [Translation, ribosomal structure and biogenesis].	8.90789e-26
NZ_CP019688.1\|WP_095659542.1\|766859_767156_-\|metal-sensitive-transcriptional-regulator	gnl\|CDD\|376835	pfam02583, Trns_repr_metal, Metal-sensitive transcriptional repressor. This is a family of metal-sensitive repressors, involved in resistance to metal ions. Members of this family bind copper, nickel or cobalt ions via conserved cysteine and histidine residues. In the absence of metal ions, these proteins bind to promoter regions and repress transcription. When bound to metal ions they are unable to bind DNA, leading to transcriptional derepression.	2.96615e-34
NZ_CP019688.1\|WP_095661019.1\|764054_765269_-\|IS481-family-transposase	gnl\|CDD\|366234	pfam00665, rve, Integrase core domain. Integrase mediates integration of a DNA copy of the viral genome into the host chromosome. Integrase is composed of three domains. The amino-terminal domain is a zinc binding domain pfam02022. This domain is the central catalytic domain. The carboxyl terminal domain that is a non-specific DNA binding domain pfam00552. The catalytic domain acts as an endonuclease when two nucleotides are removed from the 3' ends of the blunt-ended viral DNA made by reverse transcription. This domain also catalyzes the DNA strand transfer reaction of the 3' ends of the viral DNA to the 5' ends of the integration site.	5.91195e-25
NZ_CP019688.1\|WP_095659544.1\|769396_770005_+\|cation-transporter	gnl\|CDD\|224151	COG1230, CzcD, Co/Zn/Cd efflux system component [Inorganic ion transport and metabolism].	5.1355e-36
NZ_CP019688.1\|WP_095659545.1\|770089_771253_-\|MFS-transporter	gnl\|CDD\|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	9.61631e-49

>NZ_CP019688.1|WP_095658980.1|765270_766620_+|IS256-family-transposase
MTTVSPKKSHDPARVNEISEKLMDNPELAKLIGELSTSTDDASELVKGLLQASINAGLQAEMDAHLGYEHSDRKAKAEVDTRGEDNHRNGSYTKTVDSGYGPLEVTMPRDRAGTFAPQMVPKGARRLTELDDMIISLYAGGMTVRDIQHHLATTLGVDMSPDTISTITDAVLDEVMMWQNRQLEEFYPVIFLDALRIKIRDGNRVVNKSCYMAVGVDMDGIKHILGLWIAGNEGAAFWASVCADLANRGVQDVFIVCCDGLKGLPDAVEATWPNSMVQTCIVHLIRAANRWVSYQDRKPVSSALREVYTAPNEDTARAALDAFEASELGRRYPQSVKVWRDAWEQFVPFLQFPPAARRVLYTTNAIESLNAELRKATRNRGQFPNDTAALKTLWLMICNIEDKRAAQRAKKAKRAIECNGYIEGAKATGWKQAINQLAVAYPDRFADYL
>NZ_CP019688.1|WP_095661019.1|764054_765269_-|IS481-family-transposase
MGETPSDQSLTHKTPDTLAVRDQKQKVAAVAKRFGVSRQRVYQILADYDAGGDAAVAPKSRAPHTHPQAVPEALRNDIIDMRKQLTRHGLDAGPETIAYHLAAQDKRVPSTSTIRRILTDAGLVTPEPKKRPKSSYIRFEAALCNEIWQADITHVFLADGTRVEVLDFIDDHSRYLMSITAAAAFSGAAVAAELTRLISTYGPPASTLTDNGLVFTARLAGRKGGRNAFEKVLTANRIQQKNGRPGHPQTQGKIERFHQTLKKWLAARSPAPTINELQHLLDEFADYYNTQRPHRALGRRTPAQVYTTGAKASPRDNPKEEWRIRNDTVCTNGKTTVRYAGKLFHLGIGRAYASKKILMVITDKHIITSLADTGEVITEHYIDTSRDYQKPYWKTGDPPLNPHQ
>NZ_CP019688.1|WP_095659541.1|762547_763813_+|hypothetical-protein
MGSPSLIILLIVVVWVIVLAPLAFGNNKPIRRSGQGYEETRVLHEGGTMPMVERRRPKLTAADVHHYEASEDEDYELVEAVSDEEQVLIDDTSASMKTLISRTAGVSRKLAPNVIEADEVEEVKEAEAAEGAEGAEGTVESNEVEAPAAGGSTAYSVLQAQAEDSDEDEDEDEAQAEYELAESYLAPADFGYVSEEASAAAEDQAVVLEHGETDTEDNAADSDIEVAADADTSSVELEDADIAFAEARKGRGGYDPQRDALTRADRLKRRKITFISLLAASAITLIAALIVGGWMWVLPAITVGLTLWFMVALRRVVKQEQELRARRMRQLRRARLGVDTEDRPAIVERERYRAGAVIMDLDDESPDFDHLPRYRQAEPEYGTIERERRVPVRVGGRYDDFGDDDSYDDYESYGDFGDRAS
>NZ_CP019688.1|WP_095659540.1|761763_762423_+|GNAT-family-N-acetyltransferase
MLDRFIAPFRAPTPGWPETTPAVRIRDGASVQLRPLASSDGEAWSHMRLHDESWLKPVEPTTHGTWWEAHSHASWRNNWLNLRRLAYDGTVVPMVIEVNREFAGQVTLGNIQHGAVGECWIGYWVFSPYMGRGVATAACALGTDHAIHRVGMHRVTATYLPYNPASGRVLRSCGYREEGFMRRNLHINGEWRDHHFVALNAEDYPTTAVERLAAAGRIR
>NZ_CP019688.1|WP_095659539.1|760464_761754_+|molybdopterin-molybdotransferase-MoeA
MRSVDEQLEIVIDAAVTPEPVRVGISDALGLMCAEEIAATKSLPGFHQAAVDGYAVRAVDVGGSAGLRRPEPRDDEGGAETPSASRDHTLPVVGEVAAGSQKPLRLQPKQAVRVATGAPLPTLADAVLPLEWSDRGRKRMTPTRPVGSGDFVRRPGDDIQPGDIAVRQGAVLGPAQIGLVAATGRDKVLVYPRPRVTVMSYGLELVDVERDPGLGQVYDVASYVVAAVAEEAGADVNRVGIINAEPRRLAEVIAGHVSRSELVIITGAVGGSGSDAVQDVLRELGEVDTTRVAMHPGSVQGFGLLGDERIPAFLLPSNAVSALIIAETIIRPVIRESLGKKATGRRAVRARSLRAIDSIGGRRGYVRARLMRDADTGDYLVESLGGVGGAPAHLLAGFAEANAMIRLPEGVTQVRPGEIVDVEFLQQRS
>NZ_CP019688.1|WP_095659538.1|759474_760446_+|UTP--glucose-1-phosphate-uridylyltransferase
MRNSKEESQQAAHGGVRTVVVPAAGMGTRFLPATKTVPKELLPVVDTPGIELIAEEAADLGAERLVIVVAPQKQEIMDHFGEFNVLQERLLNRGKEEQAEKVSRANELIDAVAVTQESPLGLGHAVGCAEPALDAEEDAVAVMLPDDLVLPIGVMDKMVRVREEFGGSVLCAFNVTPDEVYNYGVFDVEDAERDIEGVEVKKVRGMVEKPAKEEAPSTLVATGRYLLDRAVFDALGRIEPGKGGELQLTDAIELMIQEGHPVHVVVHRGKRHDLGNPGGYIPANVDFGLRDEKYGPALYPALKEILAEFEAEHPEVLERGQQG
>NZ_CP019688.1|WP_157731254.1|758810_759410_-|5-formyltetrahydrofolate-cyclo-ligase
MAIQRSKPGTEKDQLRREVAEGRSSLKRMPERKAQLDAEIVTYSIAAMTHFGALNQPIAAYNPLPSEPGPADYAACLNAHAQSVWLPISLAEGVLAWASTPQDGQAERQGALGITEPQGPRFNSNVLRACALVIAPAMAVDKHGLRLGKGAGYYDRALVGLDVPVAAVVYDTEFVAAVPHEAHDAPVDAVITPSGFFPL
>NZ_CP019688.1|WP_095659536.1|758137_758776_-|SAF-domain-containing-protein
MNLARFDALLHPGHHRSTVIRRVLALVLVVVAGLSMLIDAHRADPSVLIFARPVAAGAVLTEEDLTTTRLPSNVVPANAIQESELATGQILAAGASAGEVVTTTRLVGPDLIAQLVAEEPPGEDFTMVPLPLAEPDIVPMLHHGARVDVIGHGPAVIAEGGRIVTVGEEGTVLVLLRKTHAAAVAAASLVDPLTVVLSGGGYSAIPQLKSAR
>NZ_CP019688.1|WP_095659535.1|757940_758132_+|hypothetical-protein
MARARRRAKRTADVDYDRTADVPLQSADTTSDDERVVELDDNAPELLSDREFYEHERPPHHGE
>NZ_CP019688.1|WP_095659534.1|757372_757936_+|molybdenum-cofactor-biosynthesis-protein
MTTAQDSLDFLEPDEEFLRAAELETGSRPAPCALVVLVGDRRFDSPDDNTHSMVAELLTEIGLEVDAVVHTKSKKSEIRKAIETGVVGGVDLVLTIGGTGVGPRDKTPEATRAVIDKMVPGVSQAIRSSGQACGAVDACTSRGICGVSGSTVVVNLAPSRQAIRDGIATIGPLISHLISELDEHSVS
>NZ_CP019688.1|WP_095659542.1|766859_767156_-|metal-sensitive-transcriptional-regulator
MSSTSEHYGYISDKDRYLARLKRIEGQTRGLQRMIEEEKYCIDILTQISAVNSALENVAVALLQDHLKHCVTEAVNSGEGAEHKIKEASEAIARMLKS
>NZ_CP019688.1|WP_095659543.1|767163_769287_-|heavy-metal-translocating-P-type-ATPase
MHDQDTREAHTHAHHQHHDDNQHHDHEDHEGHGGHGGHSGHAGHGDHGDHVAQFRRLFWIMLALSIPVVGFNAMFADLIGYSLPEASWVPWVSPLLGTVIYFWGGWPFLTGAVDEIRQRQPGMMLLIGLAITVAFVASWLSSLGVLPHTLDFWWELAMLVVIMLLGHWIEMRSLAQTTSALDSLAALLPDEAEKVDGDEVVKVAPAELEVGDMVIVRPGSSIPADGVIVEGSAAMDESMVTGESKTVRRETGENVVAGTIATDSGLRVEVTATGDDTALAGIQKLVSDAQASSSRAQRLADTAAGWLFWFTIGAAVITAVVWSFLGRPDEAVERTITVMVIACPHALGLAIPLVVSIATERAARAGVLIKDRLALESMRNVDAVLFDKTGTLTQGEPTVTALEPVEGYSDNELLALAAAAESDSEHPLARAIVSAAEEQQLEVPRASDFSSSPAVGVRATVDGTVIEVGGPYLVEERSADELKVASTWREEGAIILHVLADGHVIGALRLADKIREESFDAVKALHAADVEVVMITGDAEAVAESVAAELGIDRVYAGVRPEDKAAKVEELQREGRTVAMVGDGVNDAPSLAQADVGIAIGAGTDVAIGSAGVILASSDPRSVLSVIDLSRETYKKMQQNLWWAAGYNLAAVPLAAGVLAPIGFVMPMSVGAILMSASTVIVALNAQLLRRLDLNPEASTARLLENA
>NZ_CP019688.1|WP_095659544.1|769396_770005_+|cation-transporter
MSTERIRRAVLIVALLNLAYFFVEFAAAIAIGSASLFADSADFLEDTAINLLVFFAVAWPAQRRRKVGAFLAVLILIPAVAAIATVIYKLLNPVPPSPEGLTGVALGALVVNLACAVILLRVRDEGSSLTTGAWLAARNDALANLLIIAAGLLTFVWATAWFDIIVGAIIAAVNLSASKEVWEESREEHDSVEEAFAEMDCD
>NZ_CP019688.1|WP_095659545.1|770089_771253_-|MFS-transporter
MKKHLYLLMTMIMVVSMSELQVAGMMPSIATDLDTSVSRVGLLVSMYSLGMALGGPAVAYMLRHIRPKLALLSVVGLYAVLEALVPLIHEYWWVAIFRILTGCLSGATFGLSVTFGAQLAESPTKIGEAISIVLGGIMVGTVFGLPLSHYVAGALSWQTSFYLLALIALCLFVASLFALPSRDPASQEASEQDLRNLRSLRLWSRYLVSLLTIGAAYGSFTYFTPLLERNSGLSPNTTTVVLLTYGLFSFIGNLVVGKFADSHAVTVLRIGHAVLIISLSIIAMFATTGWLTVTMVLLVGLAGVSMNPALVTRVAEVGGTGNLVSTVHTSVITMGVTLGTAVSALTMSIAGNDPAIAMWTGAAFACLAAIVLATQTVPFKRSAASSI
>NZ_CP019688.1|WP_095661020.1|771321_771924_-|TetR/AcrR-family-transcriptional-regulator
MGRPRMFDEKSVLDAAVSEFRVHGFTDTSTEQLCEAAGVRRSTLYNTFTSKDELFVRALQHYLETTSAAQREVLGDESLNGIERLHAYFDLMIEEEVCAAEDGHAAGCMAIGTRMTPDVARRDDRIRRLLDQGLNNQLSALSLAVRQGQADGSISKNVAPENAAQLIVSLVAGLRVMAQAGRSPGDLRSMTSLGLTALLP
>NZ_CP019688.1|WP_095659546.1|772009_772453_-|hypothetical-protein
MWTPTWWAPGAAARPESGSNSSGVALQRTVVAFTGDGELMMNGQELVTAVRYNTPMLVVLVDNEQYGTIRANQEKTYPGRVSGTQLVNPDFAEWARSMGAWAETVERNEEVPGTIERAFQKLDDGHVVLLHAKVDQDHATPEGSAEA
>NZ_CP019688.1|WP_095659547.1|772394_772985_-|DNA-3-methyladenine-glycosylase-I
MEHTYPITGPDGLTRPPWAATDPLLRDYYDTEWGMPIRDEAGMFERLALEGFQVGLSWRLILTKREALRRAFHGFDPDTVAGMEVEHLLDDASVIRNRRKLAAAVTNAQATVALREEGTDLAEFIWSYQPAETPAPRTVEEVPTRSPESEQLAKDLKSRGFTFVGPVTMYALMESVGIVDTNLVGTWRRGASGVWV
>NZ_CP019688.1|WP_095659548.1|773037_773448_+|DoxX-family-protein
MNRPAVRDFALLLLRLVLGVVFVARGYQRWFGLGMAQTARDFAAAGVPQPQISAYVVGTVELLGGVFLLIGLLTTIAASVLALMVLAAGYFVHFDHGLFVEDGGVEYPLVLAVSLFMVVVFGSGRASLDGVLTRND
>NZ_CP019688.1|WP_095659549.1|773422_774079_+|hypothetical-protein
MGCSPAMINHEDVQAALSARLDGELSALDDEVVDAHLAACAECSRFWERSLVLSKQLSKVDGQRDMVPPDLSDVIMAEVRDPFLKMEQRRALTLAIGRVALGVMAVAWALWAVKLVATGGEPDPVLASFAAVRFGVALALGLCAWRPQQVAGVLLIVGTMFTFTAGFAVRDAVLQTGEFQPALVFIPLLTSVALVWTWVADRGGELRRAWAHLNADPK
>NZ_CP019688.1|WP_095659550.1|774096_775761_-|phospholipid-carrier-dependent-glycosyltransferase
MSVTGGTIGPDLSCAQLQSFGVSTVAPNPTTPAPKPVRPKRPAPQAPVTVPWSKHDTQATIVIAAFALFTRFLGLTQPTSGGTPIFDEKHYVPQGWDMVRSSFNPVLGGIESNPGYGLVVHPPLGKQLLAMGETLFGYSPLGWRIMTALFGSAVVVFVFLLARRLSQSTSIGILAGAIALFDGVLLVASKFGMLDIFQVLFIVIASWTLAGDMRQVHQRWHDAWLAGEVQTAGPLGPRVGFRWWRFATGVLLGLALSVKWSGLYYIAFFGLLGSFWDLWLRNRYGVKKPVAGTLLRDVPSALASIVLLPAVLYLWSWRAWFASETSVYRHANVDGTVADSDWPWLNLLPPSVGNWLYYHFSVLDFHGSLTSSGGHSHPWDSKPWAWLVAARPILYYSSTGIECGNGGECREMIFLFGTPPIWWLTVPILLWAAWGWLTRQDFRVIVPFIAFAAGFLPWLAAFDRQMYFFYATALVPFTAVLIALALGNLAQKGKPVTWKWVRKLAGQQLRSGQLAVVGYMALVGAAFVYWSPILYGFMVPEDYYQSLMWLPSWK

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Crispr_ID: NZ_CP019688_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019688_2

2040881-2040967

Orphan

Consensus_repeat	Method
ATGTCCCGACTCACCTGTCAAGCATCA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019688_2

>merge|NZ_CP019688|2|2040881-2040967|CRISPRCasFinder
ATGTCCCGACTCACCTGTCAAGCATCACTCATCAAGTTAAGGTCGGCCTAAGTGTCAAGAATGTCCCGACTCACCTGTCAAGCATCA

>NZ_CP019688|2|2|2040881-2040967|CRISPRCasFinder
ATGTCCCGACTCACCTGTCAAGCATCA	CTCATCAAGTTAAGGTCGGCCTAAGTGTCAAGA
ATGTCCCGACTCACCTGTCAAGCATCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019688.1\|WP_157731350.1\|2048497_2048728_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|179269
NZ_CP019688.1\|WP_095660569.1\|2048768_2052593_-\|AMP-binding-protein	unknown	unknown	gnl\|CDD\|341253
NZ_CP019688.1\|WP_095660567.1\|2046001_2046649_-\|NAD(P)H-binding-protein	unknown	unknown	gnl\|CDD\|225462
NZ_CP019688.1\|WP_095660568.1\|2046667_2047579_-\|EamA-family-transporter	unknown	unknown	gnl\|CDD\|273359
NZ_CP019688.1\|WP_095660563.1\|2039674_2040871_-\|IS481-family-transposase	unknown	unknown	gnl\|CDD\|366234
NZ_CP019688.1\|WP_095660561.1\|2036735_2037278_-\|single-stranded-DNA-binding-protein	unknown	unknown	gnl\|CDD\|239942
NZ_CP019688.1\|WP_095660558.1\|2033802_2034453_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019688.1\|WP_095660556.1\|2032125_2033283_-\|cystathionine-gamma-synthase	unknown	unknown	gnl\|CDD\|236104
NZ_CP019688.1\|WP_095660554.1\|2028860_2031272_+\|aminopeptidase-N	unknown	unknown	gnl\|CDD\|274121
NZ_CP019688.1\|WP_095660555.1\|2031304_2031991_-\|GntR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225099
NZ_CP019688.1\|WP_095660560.1\|2034955_2036626_-\|energy-dependent-translational-throttle-protein-EttA	unknown	unknown	gnl\|CDD\|236992
NZ_CP019688.1\|WP_095660562.1\|2037454_2039428_-\|bifunctional-copper-resistance-protein-CopD/cytochrome-c-oxidase-assembly-protein	unknown	unknown	gnl\|CDD\|378238
NZ_CP019688.1\|WP_095660570.1\|2052619_2053030_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373220
NZ_CP019688.1\|WP_157731307.1\|2052985_2053654_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019688.1\|WP_095658980.1\|2041231_2042581_-\|IS256-family-transposase	unknown	unknown	gnl\|CDD\|307151
NZ_CP019688.1\|WP_095660557.1\|2033437_2033836_+\|globin	unknown	unknown	gnl\|CDD\|381280
NZ_CP019688.1\|WP_095660564.1\|2042889_2043540_-\|IS3-family-transposase	unknown	unknown	gnl\|CDD\|222853
NZ_CP019688.1\|WP_095661164.1\|2047563_2048505_-\|pseudouridine-5'-phosphate-glycosidase	unknown	unknown	gnl\|CDD\|377251
NZ_CP019688.1\|WP_157731348.1\|2043536_2043854_-\|transposase	unknown	unknown	gnl\|CDD\|366690
NZ_CP019688.1\|WP_095660559.1\|2034452_2034908_-\|acyl-CoA-thioesterase	unknown	unknown	gnl\|CDD\|238329

Protein	Function_ID	Function_description	E-value
NZ_CP019688.1\|WP_157731350.1\|2048497_2048728_-\|hypothetical-protein	gnl\|CDD\|179269	PRK01271, PRK01271, tautomerase PptA.	9.38459e-12
NZ_CP019688.1\|WP_095660569.1\|2048768_2052593_-\|AMP-binding-protein	gnl\|CDD\|341253	cd05930, A_NRPS, The adenylation domain of nonribosomal peptide synthetases (NRPS). The adenylation (A) domain of NRPS recognizes a specific amino acid or hydroxy acid and activates it as an (amino) acyl adenylate by hydrolysis of ATP. The activated acyl moiety then forms a thioester bond to the enzyme-bound cofactor phosphopantetheine of a peptidyl carrier protein domain. NRPSs are large multifunctional enzymes which synthesize many therapeutically useful peptides in bacteria and fungi via a template-directed, nucleic acid independent nonribosomal mechanism. These natural products include antibiotics, immunosuppressants, plant and animal toxins, and enzyme inhibitors. NRPS has a distinct modular structure in which each module is responsible for the recognition, activation, and in some cases, modification of a single amino acid residue of the final peptide product. The modules can be subdivided into domains that catalyze specific biochemical reactions.	3.72155e-97
NZ_CP019688.1\|WP_095660567.1\|2046001_2046649_-\|NAD(P)H-binding-protein	gnl\|CDD\|225462	COG2910, COG2910, Putative NADH-flavin reductase [General function prediction only].	4.18005e-31
NZ_CP019688.1\|WP_095660568.1\|2046667_2047579_-\|EamA-family-transporter	gnl\|CDD\|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	1.51528e-37
NZ_CP019688.1\|WP_095660563.1\|2039674_2040871_-\|IS481-family-transposase	gnl\|CDD\|366234	pfam00665, rve, Integrase core domain. Integrase mediates integration of a DNA copy of the viral genome into the host chromosome. Integrase is composed of three domains. The amino-terminal domain is a zinc binding domain pfam02022. This domain is the central catalytic domain. The carboxyl terminal domain that is a non-specific DNA binding domain pfam00552. The catalytic domain acts as an endonuclease when two nucleotides are removed from the 3' ends of the blunt-ended viral DNA made by reverse transcription. This domain also catalyzes the DNA strand transfer reaction of the 3' ends of the viral DNA to the 5' ends of the integration site.	5.71985e-25
NZ_CP019688.1\|WP_095660561.1\|2036735_2037278_-\|single-stranded-DNA-binding-protein	gnl\|CDD\|239942	cd04496, SSB_OBF, SSB_OBF: A subfamily of OB folds similar to the OB fold of ssDNA-binding protein (SSB). SSBs bind with high affinity to ssDNA. They bind to and protect ssDNA intermediates during DNA metabolic pathways. All bacterial and eukaryotic SSBs studied to date oligomerize to bring together four OB folds in their active state. The majority (e.g. Escherichia coli SSB) have a single OB fold per monomer, which oligomerize to form a homotetramer. However, Deinococcus and Thermus SSB proteins have two OB folds per monomer, which oligomerize to form a homodimer. Mycobacterium tuberculosis SSB varies in quaternary structure from E. coli SSB. It forms a dimer of dimers having a unique dimer interface, which lends the protein greater stability. Included in this group are OB folds similar to Escherichia coli PriB. E.coli PriB is homodimeric with each monomer having a single OB fold. It does not appear to form higher order oligomers. PriB is an essential protein for the replication restart at forks that have stalled at sites of DNA damage. It also plays a role in the assembly of primosome during replication initiation at the bacteriophage phiX174 origin. PriB physically interacts with SSB and binds ssDNA with high affinity.	4.54693e-15
NZ_CP019688.1\|WP_095660562.1\|2037454_2039428_-\|bifunctional-copper-resistance-protein-CopD/cytochrome-c-oxidase-assembly-protein	gnl\|CDD\|378238	pfam09678, Caa3_CtaG, Cytochrome c oxidase caa3 assembly factor (Caa3_CtaG). Members of this family are the CtaG protein required for assembly of active cytochrome c oxidase of the caa3 type, as found in Bacillus subtilis.	2.11644e-64
NZ_CP019688.1\|WP_095660556.1\|2032125_2033283_-\|cystathionine-gamma-synthase	gnl\|CDD\|236104	PRK07811, PRK07811, cystathionine gamma-synthase; Provisional.	0
NZ_CP019688.1\|WP_095660554.1\|2028860_2031272_+\|aminopeptidase-N	gnl\|CDD\|274121	TIGR02412, Aminopeptidase_N, aminopeptidase N, Streptomyces lividans type. This family is a subset of the members of the zinc metallopeptidase family M1 (pfam01433), with a single member characterized in Streptomyces lividans 66 and designated aminopeptidase N. The spectrum of activity may differ somewhat from the aminopeptidase N clade of E. coli and most other Proteobacteria, well separated phylogenetically within the M1 family. The M1 family also includes leukotriene A-4 hydrolase/aminopeptidase (with a bifunctional active site).	0
NZ_CP019688.1\|WP_095660555.1\|2031304_2031991_-\|GntR-family-transcriptional-regulator	gnl\|CDD\|225099	COG2188, PhnF, Transcriptional regulators [Transcription].	2.31167e-40
NZ_CP019688.1\|WP_095660560.1\|2034955_2036626_-\|energy-dependent-translational-throttle-protein-EttA	gnl\|CDD\|236992	PRK11819, PRK11819, putative ABC transporter ATP-binding protein; Reviewed.	0
NZ_CP019688.1\|WP_095660570.1\|2052619_2053030_-\|hypothetical-protein	gnl\|CDD\|373220	pfam14681, UPRTase, Uracil phosphoribosyltransferase. This family includes the enzyme uracil phosphoribosyltransferase (EC:2.4.2.9). This enzyme catalyzes the first step of UMP biosynthesis.	6.21132e-38
NZ_CP019688.1\|WP_095658980.1\|2041231_2042581_-\|IS256-family-transposase	gnl\|CDD\|307151	pfam00872, Transposase_mut, Transposase, Mutator family.	1.31372e-127
NZ_CP019688.1\|WP_095660557.1\|2033437_2033836_+\|globin	gnl\|CDD\|381280	cd14771, TrHb2_Mt-trHbO-like_O, Truncated hemoglobins, group 2 (O); Mycobacterium tuberculosis hemoglobin O like. The M- and S families exhibit the canonical secondary structure of hemoglobins, a 3-over-3 alpha-helical sandwich structure (3/3 Mb-fold), built by eight alpha-helical segments. Truncated hemoglobins (TrHbs, 2/2Hb, or 2/2 globins) or the T family globins adopt a 2-on-2 alpha-helical sandwich structure, resulting from extensive and complex modifications of the canonical 3-on-3 alpha-helical sandwich that are distributed throughout the whole protein molecule. TrHbs are classified into three main groups based on their structural properties and named after Mycobacterium sp. genes glbN, glbO, and glbP: TrHb1s (N), TrHb2s (O) and TrHb3s (P). This group includes a Mycobacterium tuberculosis TrHb2, Mt-trHbO, encoded by the Mycobacterium tuberculosis glbO gene, which is expressed throughout the Mycobacterium growth phase. It also includes a TrHb2 from the thermophilic Thermobifida fusca ( Tf-trHb) which has a high thermostability and at the optimal growth temperature for Thermobifida fusca (between 55 and 60 degrees C ), it is capable of efficient O2 binding and release. Tf-trHb shares a relatively slow rate of oxygen binding with Mt-trHbO.	5.23161e-58
NZ_CP019688.1\|WP_095660564.1\|2042889_2043540_-\|IS3-family-transposase	gnl\|CDD\|222853	PHA02517, PHA02517, putative transposase OrfB; Reviewed.	2.06697e-45
NZ_CP019688.1\|WP_095661164.1\|2047563_2048505_-\|pseudouridine-5'-phosphate-glycosidase	gnl\|CDD\|377251	pfam04227, Indigoidine_A, Indigoidine synthase A like protein. Indigoidine is a blue pigment synthesized by Erwinia chrysanthemi implicated in pathogenicity and protection from oxidative stress. IdgA is involved in indigoidine biosynthesis, but its specific function is unknown. The recommended name for this protein is now pseudouridine-5'-phosphate glycosidase.	1.59631e-109
NZ_CP019688.1\|WP_157731348.1\|2043536_2043854_-\|transposase	gnl\|CDD\|366690	pfam01527, HTH_Tnp_1, Transposase. Transposase proteins are necessary for efficient DNA transposition. This family consists of various E. coli insertion elements and other bacterial transposases some of which are members of the IS3 family.	0.00257017
NZ_CP019688.1\|WP_095660559.1\|2034452_2034908_-\|acyl-CoA-thioesterase	gnl\|CDD\|238329	cd00586, 4HBT, 4-hydroxybenzoyl-CoA thioesterase (4HBT). Catalyzes the final step in the 4-chlorobenzoate degradation pathway in which 4-chlorobenzoate is converted to 4-hydroxybenzoate in certain soil-dwelling bacteria. 4HBT forms a homotetramer with four active sites. There is no evidence to suggest that 4HBT is related to the type I thioesterases functioning in primary or secondary metabolic pathways. Each subunit of the 4HBT tetramer adopts a so-called hot-dog fold similar to those of beta-hydroxydecanoyl-ACP dehydratase, (R)-specific enoyl-CoA hydratase, and type II, thioesterase (TEII).	2.06677e-24

>NZ_CP019688.1|WP_095660563.1|2039674_2040871_-|IS481-family-transposase
MNSPNRNLAIVRAVRDQKQKVAAVAKRFGVSRQRVYQILADYDAGGDAAVAPKSRAPHTHPQAVPEALRNDIIDMRKQLTRHGLDAGPETIAYHLAAQGKRVPSTSTIRRILTDAGLVTPEPKKRPKSSYIRFEAALCNEIWQADITHVFLADGTRVEVLDFIDDHSRYLMSITAAAAFSGAAVAAELTRLISTYGPPASTLTDNGLVFTARLAGRKGGRNAFEKVLTANRIQQKNGRPGHPQTQGKIERFHQTLKKWLAARSPAPTINELQHLLDEFADYYNTQRPHRALGRRTPAQVYTTGAKASPRDNPKEEWRIRNDTVCTNGKTTVRYAGKLFHLGIGRAYASKKILMVITDKHIITSLADTGEVITEHYIDTSRDYQKPYWKTGDPPLNPHQ
>NZ_CP019688.1|WP_095660562.1|2037454_2039428_-|bifunctional-copper-resistance-protein-CopD/cytochrome-c-oxidase-assembly-protein
MQEKRAVKAAWPFYLAAVLVAAVIAGAVAQSFVGESLAVLGIPDPGWPTTFGLPALRGAGWMLAALAVGSFLFSAFLIPPRMVGQDLNGAPLTVDGHIASRTGAWASAGLALVGIVMIPLVLSDVSGEPLANVIFEANAWSTAIEQVQESQVWLIVAAIAAVVAAAGFVASTWWPQVALLIGAVIAIMPLALTGHSATGGNHDYGTNSFIWHLTFMLVWVGALMALVAHGRRLGPNLEPAVRRYSNIALFAFLAMLVSGLINGAIRIQLTELTDYDYGWVLIAKAVGLLALGVLGYWHRQRTIPALSKDPKAFTRLAAVEVIVMAAVTGLAATLGRTPPPPPRDPNLTQMQVQMGYNLAEPVTWGNWFTLWRFELLFSVIAILLAAFYLHLARRVEGWQVSRTVWWLLGCGAIVVTLSSRLGMHMPAAYSAHMAVHMILSMGVPVLLVLGAPLTLVRAAYPAGEFNPRQWVESFQRSTFLRVVTYPPVSLIQFIFFFYALYLFIPLYELMISEHAGHVIMNAVFLVSGYFYFWELIGPDEIPQRADAKIRLAWLWISMPVHLFMGVYLMQLNIVLAEDFYQALQLPWQPDLLADQKVGGGIAWATGSFPLVIVFGVLFRQWLLDDRAETAEVDRRAEETDDEEWRRYNEMLAQYNQS
>NZ_CP019688.1|WP_095660561.1|2036735_2037278_-|single-stranded-DNA-binding-protein
MSATIVTIHGNLVSQPEYLRVGPQDRQLTKLRIASSRRRPTGVQDEHGSEIWEDVDNLYIDAECWGSLANNCRVSLFKGAPVSVTGKLVTKTWSEEGVDETGKPVTQTRSKIMLKATQVSFDLSNYQVLHSARALREELQAQSADDLVARQDGPAFAETRISAEDVVTFDDVKEDAAAPF
>NZ_CP019688.1|WP_095660560.1|2034955_2036626_-|energy-dependent-translational-throttle-protein-EttA
MAEFIYTMKNVRRAIGDKVILDNVTMAFYPGAKIGVVGPNGAGKSSLLKIMAGIDQPNNGEAFLQPGASVGILLQEPPLNEEKTVRENVEEGLGDIFAKKQRFEEIAEEMATNYSDELMEEMGKLQEELDAADAWEVDSKIEQAMEALRCPPSEEPVTHLSGGERRRVALAKLLLSEPDLLLLDEPTNHLDAESVLWLEKHLQSYPGAVLAITHDRYFLDNVAEWICEVDRGKLYPYEGNYSTYLEKKAERLEVAGKKDQKLQKRLKNELEWVRSSPKARQAKNKARLERYEEMAAEAEQYKKLDFEEIQIPTPPRLGNKVVEVDSLDKGFDGRVLIKDLSFTLPRNGIVGVIGPNGVGKTTLFKTIVGLEQPDGGSVDVGETVQLSYVDQNRANIDPEKTVWEVVSDGLDYIHVGQNEMPSRAYLSAFGFKGPDQQKPSKVLSGGERNRLNLALTLKQGGNLILLDEPTNDLDVETLGSLENALQNFPGCAVVISHDRWFLDRTCTHILAWEGNIEEGKWFWFEGNFGDYEKNKVERLGEEAAKPSRVTHRKLTR
>NZ_CP019688.1|WP_095660559.1|2034452_2034908_-|acyl-CoA-thioesterase
MADQAVRDSQELAGNVHVHNIPLRWNDFDRYGHVTNSAYIELAQEARLAFAQENFYSRGHEFVVFVRHLEADYLRPLLPNTVTATVETQVVRVGNTSFTTRQEIKDAQGRVCCVIECVQVTVDNATTSPREITTKEIGILSQSAASSALEG
>NZ_CP019688.1|WP_095660558.1|2033802_2034453_-|hypothetical-protein
METLTVTQGERGLTTLLGRALGLDQAALARFSLVDDHVVDVFVTTPFDCLAARRVSGSASRDGAVVAANDLLNALRDAGDSGAADASREVGKARDMMWPGALPPATGFVERDIVPVGVARRLADEGRNLARQFSGPAGPPRSLLDGIVMTADADSAAPVEIPMRMIFACTALGLIPGFEAPAEIPRHLRVATAGSWVRLDAPYGSIYRNVGRLIIM
>NZ_CP019688.1|WP_095660557.1|2033437_2033836_+|globin
MDQELSLYDAVGGEEFFQKLVAGFYAQIKTDDLIGPMYPEDDWEGAEDRLRWFLSQYWGGPRMYQEQRGNPMLRRRHFPFSIGEAEADRWLDLMHNSLDQFSDEELLPVYRDQLWNHMQRVAYMMINRPTLR
>NZ_CP019688.1|WP_095660556.1|2032125_2033283_-|cystathionine-gamma-synthase
MTAQSHNGVSTQAIHAGYEPDGLYGSINTPIYASTTFAQDGLATLRGGYEYTRVGNPTITALEKTLAALEGADFGVAFASGMAAVDTVLRVLLKPGDHIVIGNDAYGGTYRLIQQVFTLWGVENTVVDITDVDAVAAAVQDNTKVIWVESPTNPLLSIADIAAISHVKQHAALVVDNTFASPYLQKPFELGADVVLHSTTKYVGGHSDVVGGVVCGKDSLIDGFEDQLRFFFGWVGSIPSPFDTYLTARGLKTLPVRMERHCDNAEAVAEFLGQQDEVAKVLYPGLESHPGHEVAKRQMRRFGGMVSVLFRTEEQAKQFCLSTKLFCLAESLGGVESLVEHPATMTHVSVTGSALEVPPELVRISVGIEDADDLIADLRQAFAAI
>NZ_CP019688.1|WP_095660555.1|2031304_2031991_-|GntR-family-transcriptional-regulator
MTTQLETRTTPKRPAYMVISDQLRAKIEAQELVAGDRLPAERELVDEFGVARMTVRHALALLQDEGIIERRRGRTGGTFVRELPPFVDLNSTEDIAVQLSAQDVALSSTVTSSGTIKAPAAVELAFDLDSGTEVFAIETVYAVRGYPIAYETTYTLPSRDPHAFAELRRQDVIAPARPSEREQARLCVTGNTLLQRITRRVYAGDTLVSFSQISVRPDALQLRTSALN
>NZ_CP019688.1|WP_095660554.1|2028860_2031272_+|aminopeptidase-N
MKTNLTRADAEARKALIDNVHYDIHVDVTGKEQFTSRTTISFCSKAGATHFDLVADEFSATLDGAPLQGRDPELSEGRHELVVDATITYNRTGEGLHKFTDPKDGKDYLYTQFEPAMAMKVFAAFDQPDLKATYDVAVTAPERYTVVLNEAVTVGEDAAAGTKTWRTRIDYPLSTYLIAIVAGEYEHVTDTYRDEANDKTIELGLYARASLMEHMDAERLFQQTKDGFDFYHANFGRPYPFGDKYDQIFCPEYNMGAMEHVGAVTFRDEYIFTSEPTPYRLERRNDTILHEMAHMWFGDLVTMQWWDDLWLNESFATWSAATAQVGIGEYPEAWTTFATVEKAWAYSQDQLPSTHPIAADAPDIETAEQNFDGITYAKGASVLKQLQAYVGYEEFFAGVRTHFDNHAYANATFDDLLAALQEASGRDLSDWAAQWLRTTGVSRLYPEITADTFTVVQESEVMRDHRVRIGLYSLIDGTVTRTHQVEVDIHGERTEIPELAGIEHDLALVNDDDLTYCLMGLAPQHQQFAIEHIGDIDDLLAKTLVWSWMWESVRGGQLPARSFVRAVAAEAGNVSHPSVQERLLAQATQAVRQYVDPAWQEEGFALLNDAFRGAEPKAIFDRALARLTPTADTVAYFTQLLETSDNQEVRWLAITNLVAAGALPLDAADEESDDTNEGAISRLRVRAAVDKQWAWDKLVNEDLTNLEARYLMDGLTFTAEGLDEFTDEYFRIAPTLWDRLTNEMAQRTLEGMYPLWAVTREAVEKPNALLADDAVPAGLRRILSEGQDRAARALRNRRVDAEA
>NZ_CP019688.1|WP_095658980.1|2041231_2042581_-|IS256-family-transposase
MTTVSPKKSHDPARVNEISEKLMDNPELAKLIGELSTSTDDASELVKGLLQASINAGLQAEMDAHLGYEHSDRKAKAEVDTRGEDNHRNGSYTKTVDSGYGPLEVTMPRDRAGTFAPQMVPKGARRLTELDDMIISLYAGGMTVRDIQHHLATTLGVDMSPDTISTITDAVLDEVMMWQNRQLEEFYPVIFLDALRIKIRDGNRVVNKSCYMAVGVDMDGIKHILGLWIAGNEGAAFWASVCADLANRGVQDVFIVCCDGLKGLPDAVEATWPNSMVQTCIVHLIRAANRWVSYQDRKPVSSALREVYTAPNEDTARAALDAFEASELGRRYPQSVKVWRDAWEQFVPFLQFPPAARRVLYTTNAIESLNAELRKATRNRGQFPNDTAALKTLWLMICNIEDKRAAQRAKKAKRAIECNGYIEGAKATGWKQAINQLAVAYPDRFADYL
>NZ_CP019688.1|WP_095660564.1|2042889_2043540_-|IS3-family-transposase
MIEYIDTYRDRFGVEAICRTLRQTECGFITSRGYRAAKTRAPSARSLSDALLIPELVKVYEDNFSVYGVRKMWKAMQRAGWDIGRDQTARLMKLAGIQGRRRGRTPITTLRTDVADCRPDLVNRDFTACAPHRLWVADITYVRTLSGFAYTAFITDVYSRKIVGVATRASMHTDELPLEAFEHALYHAGDLRAEGLVHHSDRGSQYVSIRYGCLVP
>NZ_CP019688.1|WP_157731348.1|2043536_2043854_-|transposase
MPRKYSDEFKDKAVRLAEELVELEGCSKWAAAEEIGEKLGVSAHTLNHWLKPRISAFDAQGSTDESVEDELKRLRRENNELRRANEILKTASAFFAAELARPTRR
>NZ_CP019688.1|WP_095660567.1|2046001_2046649_-|NAD(P)H-binding-protein
MKVLVLGASGQVGSVLTEAALERGHIVVGVTRSSSSRILEKLGGQLVNGDAYDAEFLTGIINSFKPDVVVSATRPSKGREAELVRGTLSVASVCAEKGVWLVVSGGAGALPVSDEPNAERVVDSGYVEDAWRDIARASADQFDALVDIFPRGRWTYVAPPSRLVEGERVGRVRKSNTALVSNEQGVSELTWLDYAGLILEEVEKPSGERLVTGGY
>NZ_CP019688.1|WP_095660568.1|2046667_2047579_-|EamA-family-transporter
MGASIEKPTENWRWVVLSASAPAVWGTTYIVTTQFLPPGYPIWSSVLRALPAGIIGLLICKQLPRGEWIWRSLIMAILNIGLWFPLLFVAAYRLPGGMASVLSACQPLFVIAFAWVLLYQSPSIWRVAWAIAGVVGVAVMVLASDSIFDPLGITAGILGTVSMALGIVMTKKWQRPTDGFTWAAWLLAWGGLLQLPMAILFEGTPPPQDLRSILGYAWLSIAGGLLTYWAWFTGLGKISAVSASFLPLLSPLVATLLGYLLLDELLTLPQWFGFLLCLTAIVLSQIAPPWGAAQTSLRGATRR
>NZ_CP019688.1|WP_095661164.1|2047563_2048505_-|pseudouridine-5'-phosphate-glycosidase
MNELRVSVSDEVRNALEEGTPILGLESNVLSHGLPFPKNVELQSACDEAIRSRGVVPAITFIDRGKLCLGATEADLERLTTANNVDKVTSRDIAVQLVRGSLGATSVSASLAICELAGVPIFASAGLGGVHRDYATTMDMSGDLYEIARRRVIVVSAGVKKFLDIPKTVEVLETLNIPAVGFHTSEFPAFYCKSSGVKLGARFDRLADLAKAARNHIELDLGSGFLALVSPSDEIALDHELVESAVQQALARAHAENVRGKDITKYVMRFIDEKTNMRSRDANFEVMVEVVSRGGGISGGTFKGEGKVVWERR
>NZ_CP019688.1|WP_157731350.1|2048497_2048728_-|hypothetical-protein
MPHVEMYYFQSPISNEQKDSFGRELAELIERYFSVSYRKVSLHLVPVDGSRWGEEVVDPIILPNIDELQVVADYLE
>NZ_CP019688.1|WP_095660569.1|2048768_2052593_-|AMP-binding-protein
MRMDLDMNSPSNSNCAGSSAEVHAVFSEASKNASPVAIIGQPGPHISMIALEALARESTYIPIDSQYPVERIRYILEDSTTRTAIIDSSADAKALGEIEGLQLVRLPLELEERLTQGFDTPTEEWPVVSLEWNGHKTAYLIYTSGSTGNPKGIAISRRNLSCQMRWLRSEGFLDPSTRILQKTPIGFDAAQWEILAPINGAIPVPSPHGAFRDPHTIVQAISDYAVNTLQAVPTLLQAIADIGGFAASPSLQKVFSGGEALSWNLVDEIRSQLPSAEIVNLYGPSECTINSSAFRFGPEMIAPTDRSSTVPLGAPAADSVFYIDVGGGIRQPTPGIEGELIICGELVGMGYVNNSEETRKKFLTVNGLPSYRSGDLVRCGDDAQLRFLGRIDNQIKLRGNRIELDEINNQYLQHPWVSKAECVVVGGGEDVPQRLEAFLQLSSNAAPLMDGRGGGVHHLSKNSRLQVKAQLSNLGVRTDLGTEVESLINEAPNELVEQLEQLAFCRKSYRTFEGDKFSLEDLVQMVRVAKQESDPLHLGIGLDRDLVDAAPLASILWGISAFKDERRLLPKYGYASPGALYSIQAYVSFGKDSPHYGQTWYFDPVEKGFKWVQDDHSPSSVTRVHLVSHEAAIRSVYEKNVREVQYFELGHLLGLLDDIFENSRYCAVFSDSPPDYVDCGKLPQDLYLGSLEIVSISSSELPDSYCHAPEVFISVDDRVSGLSRGTYAENAGQFTKISDAFVEVSDVIAINQSVYRTSSFGVGLYFLDSELDLKRQYVSLGAALHRLQSHCEAFGFMSSGYSSFSGSPLPAAIKATEILKIESESKEISFYFAVGGPISKSQRLHRGMNEDQVHMEGPAEIVTREIRDQVPSYMVPDQVTVLPALPTTPNGKVDRTALMAISEQRATSLRSSSGRAPEGEVERAIARSWGQILKCEGIKATDNFFDLGGNSVRVMMLVSSLKTVFGESVTPQLIFANPVLEELASVIKNPITQSRAIKLREMDPGGGQAQSSGRVSSLMWPGLGGLPLNLSHLADNLSAGGEIIGIQAQGINERESPVASIEQVAEQDCEFAPGEGVLHLIGYSFGCRTALTSAALLEAQGRRVDSLTLLCPGNPTLSTDGHLLIPQTGERDSSVDNPEFVGMLLSVFNHPLDPHDFQKVTATAKSLDDVVEFIQKKNHAIDPDQIERIVRLVCTQYEFDYSFEEMEAYHVSCPILLVKAKGDKYSSVDEILERNILDITTIGFDADHYEILKPPHVKELGAIISDFQSNAIHV
>NZ_CP019688.1|WP_095660570.1|2052619_2053030_-|hypothetical-protein
MKLDGTLANRQRVIHLELLTDNRGFTGKLHSQTLTPKFYYESLPDSVASSTVLLFEPMVATGRSLSLAIDRLKDVGVQETSIISVNYLASPQGLEFVQQRHPDCTYVIASIEEALTENGYMLPGIGDFGDRFFSAG
>NZ_CP019688.1|WP_157731307.1|2052985_2053654_+|hypothetical-protein
MNYPLAVRERAVELYRKGLEPRQVRTRLSDEGIDPVPSAASIWRWAVNAEHGVEVDHHWRSPSEVAAAVRAALTSPGSLREISRQCGVSSTALSIWVRNFAPDEETRRGMNPEQLEQATLWRVEQHRRRPRKSASPQTPKPTSARAAKIASEQHVTQLDDAALPDDPEELKAMLRHERFLRLADKALFEAVMESEGKAPARRRSTAWSSLKLSSDSGRTDTK

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Crispr_ID: NZ_CP019688_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP019688_3

2210966-2211062

Orphan

Consensus_repeat	Method
CCACCGAGGCGGCGGAGCCGACCAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP019688_3

>merge|NZ_CP019688|3|2210966-2211062|CRISPRCasFinder
CCACCGAGGCGGCGGAGCCGACCACTTCGGAGACTTCGACCGAATCCTCCACCACGACGACGACCGCGACTTCCACCGAGGCTGCGGAGCCGACCAC

>NZ_CP019688|3|3|2210966-2211062|CRISPRCasFinder
CCACCGAGGCGGCGGAGCCGACCAC	TTCGGAGACTTCGACCGAATCCTCCACCACGACGACGACCGCGACTT
CCACCGAGGCTGCGGAGCCGACCAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP019688.1\|WP_095659852.1\|2197322_2198786_-\|DDE-type-integrase/transposase/recombinase	unknown	unknown	gnl\|CDD\|366234
NZ_CP019688.1\|WP_095660707.1\|2213722_2214787_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|366166
NZ_CP019688.1\|WP_095660703.1\|2209114_2209849_+\|amino-acid-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224051
NZ_CP019688.1\|WP_095661182.1\|2218530_2219004_+\|acetyl-CoA-acetyltransferase	unknown	unknown	unknown
NZ_CP019688.1\|WP_095660702.1\|2208442_2209114_+\|amino-acid-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223836
NZ_CP019688.1\|WP_157731364.1\|2213168_2213324_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019688.1\|WP_095660699.1\|2204902_2206714_-\|serine/threonine-protein-phosphatase	unknown	unknown	gnl\|CDD\|277347
NZ_CP019688.1\|WP_095660695.1\|2198956_2199397_+\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP019688.1\|WP_157731362.1\|2212941_2213079_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP019688.1\|WP_157731360.1\|2211255_2211918_-\|enoyl-CoA-hydratase	unknown	unknown	gnl\|CDD\|236115
NZ_CP019688.1\|WP_095660700.1\|2206907_2207795_+\|transporter-substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|270412
NZ_CP019688.1\|WP_095660697.1\|2200237_2200696_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|368622
NZ_CP019688.1\|WP_095660706.1\|2211910_2212810_-\|polyphosphate-kinase-2	unknown	unknown	gnl\|CDD\|213852
NZ_CP019688.1\|WP_095660696.1\|2199510_2200158_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224482
NZ_CP019688.1\|WP_095660710.1\|2219298_2222319_+\|Na+/H+-antiporter-subunit-A	unknown	unknown	gnl\|CDD\|237154
NZ_CP019688.1\|WP_095660698.1\|2201091_2204868_+\|non-ribosomal-peptide-synthetase	unknown	unknown	gnl\|CDD\|274093
NZ_CP019688.1\|WP_095660701.1\|2207799_2208459_+\|amino-acid-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223836
NZ_CP019688.1\|WP_095660709.1\|2216788_2218168_+\|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl\|CDD\|236127
NZ_CP019688.1\|WP_095660708.1\|2214876_2216514_-\|chaperonin-GroEL	unknown	unknown	gnl\|CDD\|234573
NZ_CP019688.1\|WP_095660711.1\|2222319_2222811_+\|Na(+)/H(+)-antiporter-subunit-C	unknown	unknown	gnl\|CDD\|236136

Protein	Function_ID	Function_description	E-value
NZ_CP019688.1\|WP_095659852.1\|2197322_2198786_-\|DDE-type-integrase/transposase/recombinase	gnl\|CDD\|366234	pfam00665, rve, Integrase core domain. Integrase mediates integration of a DNA copy of the viral genome into the host chromosome. Integrase is composed of three domains. The amino-terminal domain is a zinc binding domain pfam02022. This domain is the central catalytic domain. The carboxyl terminal domain that is a non-specific DNA binding domain pfam00552. The catalytic domain acts as an endonuclease when two nucleotides are removed from the 3' ends of the blunt-ended viral DNA made by reverse transcription. This domain also catalyzes the DNA strand transfer reaction of the 3' ends of the viral DNA to the 5' ends of the integration site.	7.02925e-10
NZ_CP019688.1\|WP_095660707.1\|2213722_2214787_+\|alpha/beta-hydrolase	gnl\|CDD\|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	0.000469653
NZ_CP019688.1\|WP_095660703.1\|2209114_2209849_+\|amino-acid-ABC-transporter-ATP-binding-protein	gnl\|CDD\|224051	COG1126, GlnQ, ABC-type polar amino acid transport system, ATPase component [Amino acid transport and metabolism].	6.00718e-135
NZ_CP019688.1\|WP_095660702.1\|2208442_2209114_+\|amino-acid-ABC-transporter-permease	gnl\|CDD\|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	4.14485e-58
NZ_CP019688.1\|WP_095660699.1\|2204902_2206714_-\|serine/threonine-protein-phosphatase	gnl\|CDD\|277347	cd07402, MPP_GpdQ, Enterobacter aerogenes GpdQ and related proteins, metallophosphatase domain. GpdQ (glycerophosphodiesterase Q, also known as Rv0805 in Mycobacterium tuberculosis) is a binuclear metallophosphoesterase from Enterobacter aerogenes that catalyzes the hydrolysis of mono-, di-, and triester substrates, including some organophosphate pesticides and products of the degradation of nerve agents. The GpdQ homolog, Rv0805, has 2',3'-cyclic nucleotide phosphodiesterase activity. GpdQ and Rv0805 belong 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.	3.29911e-15
NZ_CP019688.1\|WP_095660695.1\|2198956_2199397_+\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	9.9763e-15
NZ_CP019688.1\|WP_095660710.1\|2219298_2222319_+\|Na+/H+-antiporter-subunit-A	gnl\|CDD\|237154	PRK12644, PRK12644, putative monovalent cation/H+ antiporter subunit A; Reviewed.	0
NZ_CP019688.1\|WP_157731360.1\|2211255_2211918_-\|enoyl-CoA-hydratase	gnl\|CDD\|236115	PRK07854, PRK07854, enoyl-CoA hydratase; Provisional.	2.61097e-64
NZ_CP019688.1\|WP_095660700.1\|2206907_2207795_+\|transporter-substrate-binding-domain-containing-protein	gnl\|CDD\|270412	cd13694, PBP2_Cysteine, Substrate binding domain of ABC cysteine transporter; the type 2 periplasmic binding protein fold. This subfamily comprises of the periplasmic-binding protein component of ABC transporter specific for cysteine and its closely related proteins. The cysteine-binding domains belong to the type 2 periplasmic binding protein fold superfamily (PBP2), whose many members are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two receptor cytoplasmically-located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	2.55897e-110
NZ_CP019688.1\|WP_095660697.1\|2200237_2200696_+\|hypothetical-protein	gnl\|CDD\|368622	pfam05808, Podoplanin, Podoplanin. This family consists of several mammalian podoplanin like proteins which are thought to control specifically the unique shape of podocytes.	0.0021836
NZ_CP019688.1\|WP_095660706.1\|2211910_2212810_-\|polyphosphate-kinase-2	gnl\|CDD\|213852	TIGR03707, PPK2_P_aer, polyphosphate kinase 2, PA0141 family. Members of this protein family are designated polyphosphate kinase 2 (PPK2) after the characterized protein in Pseudomonas aeruginosa. This family comprises one of three well-separated clades in the larger family described by pfam03976. PA0141 from this family has been shown capable of operating in reverse, with GDP preferred (over ADP) as a substrate, producing GTP (or ATP) by transfer of a phosphate residue from polyphosphate. Most species with a member of this family also encode a polyphosphate kinase 1 (PPK1). [Central intermediary metabolism, Phosphorus compounds].	5.14393e-149
NZ_CP019688.1\|WP_095660696.1\|2199510_2200158_+\|hypothetical-protein	gnl\|CDD\|224482	COG1566, EmrA, Multidrug resistance efflux pump [Defense mechanisms].	0.00253775
NZ_CP019688.1\|WP_095660698.1\|2201091_2204868_+\|non-ribosomal-peptide-synthetase	gnl\|CDD\|274093	TIGR02353, NON-RIBOSOMAL_PEPTIDE_SYNTHETASE, non-ribosomal peptide synthetase terminal domain of unknown function. This domain is found exclusively in non-ribosomal peptide synthetases and always as the final domain in the polypeptide. This domain is roughly 700 amino acids in size and is found in polypeptides roughly twice that size.	0
NZ_CP019688.1\|WP_095660701.1\|2207799_2208459_+\|amino-acid-ABC-transporter-permease	gnl\|CDD\|223836	COG0765, HisM, ABC-type amino acid transport system, permease component [Amino acid transport and metabolism].	4.4304e-63
NZ_CP019688.1\|WP_095660709.1\|2216788_2218168_+\|M20/M25/M40-family-metallo-hydrolase	gnl\|CDD\|236127	PRK07907, PRK07907, hypothetical protein; Provisional.	0
NZ_CP019688.1\|WP_095660708.1\|2214876_2216514_-\|chaperonin-GroEL	gnl\|CDD\|234573	PRK00013, groEL, chaperonin GroEL; Reviewed.	0
NZ_CP019688.1\|WP_095660711.1\|2222319_2222811_+\|Na(+)/H(+)-antiporter-subunit-C	gnl\|CDD\|236136	PRK07946, PRK07946, putative monovalent cation/H+ antiporter subunit C; Reviewed.	2.30933e-73

>NZ_CP019688.1|WP_095660703.1|2209114_2209849_+|amino-acid-ABC-transporter-ATP-binding-protein
MELLKLHDVRKTYPNGHRALDGVSLSVDRGEVVAIIGPSGCGKSTLLKTVNGLEPVDSGHILVDGRDVTLATTRLKDVRADVGMVFQSYDLFPHLTVMKNLLLAPKVVQGANEAQARERAMELLERVGLADKADARPRELSGGQQQRVAIVRALMMEPKALLLDEITASLDPEIVREVLEVVVGLARDGMTMLVVTHEMSFAKAVADRVVFMDAGRIVEVAPPEEFFASPSSDRAKRFLDQLVF
>NZ_CP019688.1|WP_095660702.1|2208442_2209114_+|amino-acid-ABC-transporter-permease
MFSDLEVLAQGNNFARLLQGLGVSVQIALISMALSIVLGTLLGVVMTSKSKIVRVVTQFYLQFVRIMPQLVLLFLVYFDLTRGFGINLDAKVAAIIVFTLWGTAEMGDLVRASIQAVPRHQYLSAAALGIEGRDLYRHVVLPQAVRGLLPLTINLTNRMIMTTSLVALIGVVEVLKVAQQIIDANRFDYPSAALWIYGVVFVLYFLVCFPISLAARKLEERWQ
>NZ_CP019688.1|WP_095660701.1|2207799_2208459_+|amino-acid-ABC-transporter-permease
MDFSVVADNIPVYAQAAVLTVRVAAKGILLAFLVGALCATIRYFRIPVLRQLTTAYIEVSRNTPLLVQLFFLYFGLPKLGIVIESETCAVIGLGFLGGSYMAEAIRAGLEGVPASQMQSSLSLGMSRTQALRHVITPQATALALPALTANIIFLIKETSVVSIVALPDLVYTAKEQIGQTYETREALLLLVTFYLIILLPISLVAGAVERKVRANVFGS
>NZ_CP019688.1|WP_095660700.1|2206907_2207795_+|transporter-substrate-binding-domain-containing-protein
MSIIPNRKRIAAGVAAVLAAVSLTACSSDSSGSSDSAGSDAPSASSSFRDVDAIKEDGTVKIGVFSDKAPFGYVDANGGYAGYDIEYGNRLGEDLGVEVEYVPVEAASRVEFLDTNKVDIILANFTVTPERQEKVDFANPYMKVSLGAVTPDAKPLNSVEELEGKNVIVVKGTTAEAYLEENHPEIKLTKFEQYTEATNALIDGRGDAWVTDNTEALAWAEQTPGFTATIPTLGDIDTIAGAVAKGNTSLKDWMNDELVELGKENFFHDAYEKTLKPVYGDAVSADDLVVEGGKL
>NZ_CP019688.1|WP_095660699.1|2204902_2206714_-|serine/threonine-protein-phosphatase
MTLRNSFLATATATAIATATVIALPLGLTQAVAAQPETLPASARPYLYFESFDAVPNPAHFTHDMPKGWKQDVTGVTSGEERWNGWTLSTIRRWTWTSGTEQRHYFTQGHDQVAIIDSKQQRLAPRDSMDASLTSANINVSGQGTVALEFDHHYRQGKSGQTAQVSVSFDGGAQQTVATFDADRYSSHEYFEIDVPAGASQMQVTFSYLGGNDDYWWALDNVAVRAPFTQVAEQPKAIIDVISDTQDDPEDFKLAVARLNAMPEKADALVINGDLVDLGTQEQWDTFLAAREAMPHDSGEEFWTIGNHELYGHELDFQEKMDRYMQYAGEHTGQDKPWFEKVVDGVPMIGISTEYYQDSDRDGKEPFQRLSAEQLAWLDSRLAYWDSQGVTALVFTHPLLPQTVSMSHSAWYQNDFENQQALSNVLSKYNDVVAFTSHSHASLYQNNWWGTRRYDGTQEGAIGFPVVNTGAILNEYMPDGDHDEEIVDEQAASGLRVKIYDDRVRVEAWDFKAGHSATNPEGTTKLIKYQDFSKQGRLTASDAVRNQAAGAGSNAGSQPSPNPQQDGSTGSSGSGMPAAVGVIVAVLAALGGLFAFFAPQVVR
>NZ_CP019688.1|WP_095660698.1|2201091_2204868_+|non-ribosomal-peptide-synthetase
MTIQGNHDEHLLRAHLAPPPRTLVDIVRATAEEHPEAAAIDDGEVLTYAELIAEVEALAADLHAHGLDHGGRVGIRMTSGSKDLYLAILATMFAGCAYVPVDADDPDERAELVFGEAKIDAVWTDEGFRVLRGSKAVQGGVDKQVSPDDDCWIIFTSGSTGTPKGVAVTHRSAAAFVDAEARLFCQAEPLGPDDRVLAGLSVAFDASCEEMWLAWRHGACLVPAPRALVRSGQDLGPWLIRRDITVVSTVPTLAGLWPAEALDNVRLLIVGGEACSQELTDRLATGREMWNTYGPTEATVVASAQRLVPGEPVTIGWALDGWDLKVADDGELVIGGVGLARYLDPAKDAEKYAPMGDWPRAYRTGDHVKIADNGLAFIGRADDQVKIGGRRIELGEVEAHVAGLDGVYNSAVSTQTLPSGDKVLVGYLSPDPGVTLDVIAMREALAEVMPAALVPRLHVMDELPVRTSGKVDKKALPWPLPAEVSAVGLTETEAWVAQTFVDVLGMDVASRDDDFFALGGTSLAAATLVARLRERVPTIAVRDLYDHPRLGALASLIDDSLGTTHTLRDRAVTPVGATTRLAQTLLMVPVMTLRAATAVTWVLLAAQLLGVLALSWSGLVLAFVVFCTPLGRVPVGALGARVIRGRIEAGVYPRGGAVHVRLWAAERWLAASGATNISAAWLVKPLARMLGARIGRGVDFQTLPPVTGLLTVGSGAAIEPGVDLSGHWLDGDELHVGAVTIGDDARIGARSTLMPGTEIRQDAHVEAGSTVTGDKPVKKGARWAGSPAKKVGRSKLRFPDERPPRGIVWAAAYALTSLALAGLPVAAAAAGIAVVWALAPSIGWAVVLSPLGGLVYQGVGMGLTWLGVRIAQLSIKPGIAPVRSRHGLALWTVVRLMDDARTRFFPVYAALLTPVWLRTLGAHIGNDAEVSTAVMVPTLTEVRDGAFLADDTLAGGYELGGGWIRSAQTTVGRRAFVGNSGMVAPGRKLAKQSLVAVLSASPKKSKAGSNWWGSPPERMRRVEVEAGSESVTYAPSTSMKLRRGFVETLRLLAPMAHAWLAALFAVVVVGLTPVLGWWVYLAGGLVWMYIGALAVLVAVATKWLLVGTHRAGEHPLYSWFVWLNELQDQFIELVAAPWFFNWAPGTGEMSLVLRLLGVDIGRGAWVESYWFPETDLCRVGDGASVGRGTVVQTHLFQDRVMSLDAVVVEAGASVGPHSVVLPGAVIGADASVGPGSLVMRGDVLSERTVWQGNPVEPR
>NZ_CP019688.1|WP_095660697.1|2200237_2200696_+|hypothetical-protein
MTRSRIRTAGVAAAVATSLIVAPNAFAEDNATTAAETVDAQNVEQQTPKEDAPKEDTPKEDTPKEDTPKEDTPKEEEEKEPKGDRSSNNTIQSSKEGDKTAKGSSEDGSLSPGAIAGIVIGVLAAIAGAAAFALPQIQQFLPPQIQQFLPKF
>NZ_CP019688.1|WP_095660696.1|2199510_2200158_+|hypothetical-protein
MKRFRAASIAAALSAALITAPIPFASAETPNAEIAAEENKNAAEDTNPELIAAEAALERAEKKLNEAKAELTKIEQDAIEARKAESEALKKATGDQAGKFEAARIDNEHERSKKILAAMEKVTKAQADYDRAAAEVERVKAGPSNDRNERESINQPLVTQVPKNTKGSATSSSELSGVNPVAGGAVIGLAIGIIAAIFSVVAVTLPMLPQIAAAF
>NZ_CP019688.1|WP_095660695.1|2198956_2199397_+|MarR-family-transcriptional-regulator
MAQSADLPHSLTRSPSFQIERVRRHTKDEVERALSQHGSSMREFWILSCVVDQPYSQTQLSELLAIDASDMVRLVDSLEKHEWVKRDRDPRDRRRQIVTPTKKGIKAHASLVDDVASAEDRALDMSTTKQLKSLKKLSKAILEEES
>NZ_CP019688.1|WP_095659852.1|2197322_2198786_-|DDE-type-integrase/transposase/recombinase
MAIPLHKRRKVADFDPVRDGKTITQFCKELGISRQTYTNIKKRVAQKGRSGILPDSTAPKNPARRFDEADKIAVVNARQHLMEQGLDYGPWSIYYSLFDSVGPDRTPSRSTIALWLHELGFVEANARKRPRSSYKRFARDFVGELWQIDGLVYRLFDHAHTHVTIYQVIDDASRFDVGTKAFALPENGTDARAALAEAFAVYGKPQEILSDNGEAFATYHRGHLSATEVWLASEGVLAIAGFAPTTQGKDERSHRTLIQFLDARHPVSLAEVNSYLVEYRQVYNERRRHQSLLVGKMHITPRQAFDTFPKAAPPTHPLDPENVWARVVTFNQAHNPQAALIATNGPGQAATSPEASTDDMAAQQGIPPTDTPTLTMPTTRSTNSWGIPDELRVSKDGVVRVLAHGLYIGLRFKNRLLYTTVTADNVAEFFTAHDGEFLFSVPLPITLSHRPPGGQININLVEGMKHRQPPQLKPNLSKPRPKRRPQR
>NZ_CP019688.1|WP_157731360.1|2211255_2211918_-|enoyl-CoA-hydratase
MIKVVDSGPVRVISLDRHEKRNALSQELCTLLIDGILHPPSSTRAIVLTGEGTVFSAGADLDETDFQDALYPVIAKLMRTIVASPLPAVAYLNGPAIGAGMMLAMACDLRVVSETAVCSLPVTKIGIGVDSWPVEALAELIGGARARAMLLAGLPLDVDTAVATGFAVGRGSLEDALAFAGNFAGKSAETVANVKQQFAPSLFTEAERDAGVQAAWDARP
>NZ_CP019688.1|WP_095660706.1|2211910_2212810_-|polyphosphate-kinase-2
MADHNDDDMPMIDLAATEGWIVDDSDEDDPVLLMPDGTPIQTWREQYPYEERMSRDEYEEKKRALQIELLKWQNWTKDTGQRHIILFEGRDAAGKGGTIKRFNEHLNPRGARTVALEKPSPRESTSWYFQRYIEHFPAAGEIVFFDRSWYNRSGVERVMGFCTESQHAEFLREVPMLENMILGSGISLTKFWFSVTQKEQRTRFAIRQVDPVRQWKLSPMDLASLDKWDDYTRAKEETFRYTDTDESPWITIKSNDKKRARLNAMRYILSKFEYTNKDHEIVGEPDPKIVKRGRDQIGD
>NZ_CP019688.1|WP_157731362.1|2212941_2213079_-|hypothetical-protein
MENITTALENWKFVSSDAHLAGALLDILKSLAGAAENAHKLLGLL
>NZ_CP019688.1|WP_157731364.1|2213168_2213324_-|hypothetical-protein
MDLSAIISALKDFETFGKNIVGLFRFVPDFLLKLTELGDKQTGLAPEAKAN
>NZ_CP019688.1|WP_095660707.1|2213722_2214787_+|alpha/beta-hydrolase
MAAEWHELHPGEAPAAPAGAATYRVIYPAPGARSEVTMSGLVTVPESTAATEAGTAVPLLSFAHGTTGISTSSAPSLYKEGDPIGRYIERSTVFLQSWVDAGFTVLQPDYEGLGVEEVGGTYLHRASSAGAINGLVETAKKRFDAQHWVNVGYSQGGYSALAAADNPTEGLMATVAIAPGDTELVNKNLRIMGIGPVDVARMLSGRAVRFFPIVLASAMNAFEDVDGDAFLSDLGRELVAKANTLTLPELEEEVEDISGGDLFFSNADTTVLQARLDEQRLELMHPQGPVLVLVGNQDTTINREHVIGQVNAWEAAGVEVKYVELDGVGHGKSISEAQAPIHEWVAQRDGRAAR
>NZ_CP019688.1|WP_095660708.1|2214876_2216514_-|chaperonin-GroEL
MAKMIAFDEEARRSLENGLNTLADAVRVTLGPKGRNVVLEKSWGAPTITNDGVTIAKEIDLEDPYEKIGAELVKEVAKKTDDVAGDGTTTATVLAQALVREGLRNVAAGSNPMGIKRGIQAATEKVSQSLLNSAKEVETQEEIASTAGISAGDPEIGKKIAEAMYAVGNGSVNKESVITVEESNTFGVELEVTEGMRFDKGFISAYFATDMERGEAVLEDPYILLVSGKISNVKELVPVLEQVMQSGKPLLIIAEDVEGEALSTLVVNKIRGTFKSVAVKAPGFGDRRKAMLQDLAILTGGQVISEEVGLSLETAGIELLGQARKVVVTKDETTIVQGSGDQAQIEGRVKQIRAEIENSDSEYDREKLQERLAKLAGGVAVIKVGAATEVELKEQKLRIEDAVRNAKAAVEEGIVAGGGVALLQAAKELEGDLGLEGDEATGVRIVREALSAPLKQIALNAGLEPGVVADKVAHLPEGEGLNAATGEYINMLANGIADPAKVTRSALQNAASIAALFLTTEAVVADKPEPAGAGAGMDPEAMGMM
>NZ_CP019688.1|WP_095660709.1|2216788_2218168_+|M20/M25/M40-family-metallo-hydrolase
MSNDNAVNSAVTSTDFTFSPNRERIFQELAELISHYSPHSMPEHAATHEEAAKWVTAKLEELGLDVTRHPTVDDADTIIGVKEPVGDAPTVLLYSHYDVVPAQNPAVWTNDPLELDERGGRWYGRGAADCKGNVIMHLAALRMVQENGGTDLGIKVVVEGSEELGGEDGLGKLIDANPELFTADVIFIGDGGNVAVGIPTLTTHLRGGAQLRIKVDTLEGPVHSGGWGGAAPDAAHALIRISDSFFDEHGRTTIEGVDTTAKWEGDPYDRETFRKDARVLDGVQLLGTVDDEPADMVWARPAITVIGFTSVPVKDATNIVNSTAEAQFNLRVPAPQSAAEVAKKVEEQIYARAPWGAKVEVSVTGVNEPFSTDPNGPAVQHFGKCMQDAYGAERLTVVGTGGSIPLTVTLQKHFPDAEFALYGVADPAANIHGIDESVDPTEIEHVAIAEATFLLTYGK
>NZ_CP019688.1|WP_095661182.1|2218530_2219004_+|acetyl-CoA-acetyltransferase
MEPDPLKARYEIDANLPRELRHEARDMDWGLFIATYAPEPTLKVTLTACKQKDWMKSEYSFDVYASPKASASQNFHETIEATGPVRAISQLLDRHRRYVEILAFHQIEIFEATATCLKVGHSERDLRKAWVIGFGGTPEASAAAAMSAGAQRIHGNL
>NZ_CP019688.1|WP_095660710.1|2219298_2222319_+|Na+/H+-antiporter-subunit-A
MLTLLIALFATTVAAPVLLRVIGRPAFGILAIVPAVGFGWMVSLFNRGVFRDGGEIVAAFQWMPSTHLNLEFRLDALAALFSLIILGVGALVLFYCWGYFDQNPRRLAKFAAELTMFATVMYGLVISDNFLLMYVFWELTSVLSYLLVSYYGERASSRRAAIQALLITSFGGLAMLVGINLLGAQTGIWKLSEISQFADLEATTGISVAIVLIMLGALTKSAQAPWHFWLPGAMAAPTPVSAYLHSAAMVKAGIYLVARLAPDLAAVQTWHLVVLTTGCATMLLGGWMALKQRDLKLILAYGTVSQLGFITAVIGIGSREATMAGLALTFGHSLFKATLFMVVGAIDHATGTRDIRKLSGLGKKEPIIAILAIVSAASMAGIPPLFGFVAKEAALEAVLHEELLTGMPGKITLVVLVVGSILTMAYSLYFLHGAFATKGDVEDVDDKGYSPVVREMHDIVPTMWLSPLVLTICTVVFGMFPAWFSGAFNDYLGVRFPAVDKQELKLWHGVTVPLILTVVIVAAGAVMFWQRDLVRRAQPERPALGDADAVWDNLLSALRTLSLRLTASTQRGSLTINLAVIFATLMVVQLAYLILGESNSIRMILWDSTWQGIVVIIMVAMAVFATLQNNRLSALVMVGLTGYSLAMIFALHGAPDLALTQALVETIVMVIFMLVLRKMPTEVEPRTDDNRLRAWLSIGVGLSVTIVGMTAMSARVAEPISKDMPDLAYEIGHGRNTVNVLLVDLRAADTFGEILVLVIAATGVASLIFGTGKFGRASRRPTLSTTKARWLAAGVATETEQNRSIMVDVVTRILFPSMMLLSVYFFFSGHNAPGGGFAGGLVAALAFSLRYLAGGREEIEEALPVDPAKLLGTGVMISFIAVVTPMFFGYPPLISNYVTLELPLIGEFDVPSALVFDAGVYVIVIGLIMHVLTSMGAYLDREEDLRKERARDRARELQEKNLKRRGKQARLRQARQEERAGFATAGSTAVGTTTLDTRDATKEGND
>NZ_CP019688.1|WP_095660711.1|2222319_2222811_+|Na(+)/H(+)-antiporter-subunit-C
MEANLFLLIGSGVLITCGVYLMLDRALTKMIMGVLLIGNGGNLLLLQAGGQAGSPPILGRSSEVVAEMADPLAQAMILTAIVISMALAGFMLSLAYRQYRYRTDDIIERDEEDRAVATRPTTPSAAPDHDASDDPETGRLSSSGDAFGPHFFENPVREADGER

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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

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

1956227 : 2010748

Streptococcus_phage(22.22%)

protease,tRNA

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_095660487.1\|1956227_1957523_+\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_095660488.1\|1957523_1958309_+\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_095660489.1\|1958309_1959101_+\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_095660490.1\|1959039_1960287_-	phosphatase PAP2 family protein	NA	NA	NA	NA
WP_157731340.1\|1960309_1961530_-	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_095660492.1\|1961546_1963511_+	hypothetical protein	NA	NA	NA	NA
WP_095660493.1\|1963542_1965399_-	elongation factor 4	A0A2K9L6L3	Tupanvirus	4.5e-20	37.7
WP_095661161.1\|1965624_1965981_+	hypothetical protein	NA	NA	NA	NA
WP_095660494.1\|1966153_1966417_+	30S ribosomal protein S20	NA	NA	NA	NA
WP_095660495.1\|1966413_1966776_-	ankyrin repeat domain-containing protein	NA	NA	NA	NA
WP_095660496.1\|1966827_1967436_-	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_095660497.1\|1967532_1967970_+	DUF1772 domain-containing protein	NA	NA	NA	NA
WP_095661162.1\|1968014_1968449_+	hypothetical protein	NA	NA	NA	NA
WP_095660498.1\|1968445_1969384_-	DNA polymerase III subunit delta	NA	NA	NA	NA
WP_095660499.1\|1969385_1971002_-	ComEC/Rec2 family competence protein	NA	NA	NA	NA
WP_095660500.1\|1970998_1971652_-	ComEA family DNA-binding protein	NA	NA	NA	NA
WP_095660501.1\|1971744_1972677_-	hypothetical protein	NA	NA	NA	NA
WP_095660502.1\|1972718_1973513_-	DegV family EDD domain-containing protein	NA	NA	NA	NA
WP_095660503.1\|1973512_1974187_-	histidine phosphatase family protein	NA	NA	NA	NA
WP_095660504.1\|1974180_1974651_-	ribosome silencing factor	NA	NA	NA	NA
WP_095660505.1\|1974719_1975331_-	nicotinate-nucleotide adenylyltransferase	NA	NA	NA	NA
WP_095660506.1\|1975327_1976611_-	glutamate-5-semialdehyde dehydrogenase	A0A1X9I5D4	Streptococcus_phage	1.4e-84	44.9
WP_095660508.1\|1977100_1978012_-	hypothetical protein	NA	NA	NA	NA
WP_095660509.1\|1978046_1978466_-	low molecular weight phosphatase family protein	NA	NA	NA	NA
WP_157731410.1\|1978495_1979590_-	ACR3 family arsenite efflux transporter	NA	NA	NA	NA
WP_095661163.1\|1979600_1979975_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_095660510.1\|1979981_1981103_-	glutamate 5-kinase	A0A1X9I5D0	Streptococcus_phage	2.3e-56	40.8
WP_095660511.1\|1981103_1982603_-	GTPase ObgE	NA	NA	NA	NA
WP_095660513.1\|1983417_1984173_+	hypothetical protein	NA	NA	NA	NA
WP_095660514.1\|1984243_1984588_-	50S ribosomal protein L27	NA	NA	NA	NA
WP_095660515.1\|1984603_1984909_-	50S ribosomal protein L21	NA	NA	NA	NA
WP_095660516.1\|1985195_1985612_+	hypothetical protein	NA	NA	NA	NA
WP_095660517.1\|1985620_1986154_+	sigma-70 family RNA polymerase sigma factor	A0A0F6TH34	Sinorhizobium_phage	3.0e-09	31.1
WP_095660519.1\|1988570_1990031_-	hypothetical protein	NA	NA	NA	NA
WP_095660520.1\|1990033_1991860_-	hypothetical protein	NA	NA	NA	NA
WP_095660521.1\|1992137_1993457_+	hypothetical protein	NA	NA	NA	NA
WP_095660522.1\|1993513_1996684_-	Rne/Rng family ribonuclease	NA	NA	NA	NA
WP_095660523.1\|1996877_1997288_-	nucleoside-diphosphate kinase	A0A167REB2	Powai_lake_megavirus	1.1e-27	47.4
WP_095660524.1\|1997312_1997618_-	hypothetical protein	NA	NA	NA	NA
WP_095660525.1\|1997635_1998085_-	DUF4233 domain-containing protein	NA	NA	NA	NA
WP_095660526.1\|1998131_1998986_-	RimK family alpha-L-glutamate ligase	NA	NA	NA	NA
WP_095660527.1\|1998982_2000434_-	dihydrofolate synthase	NA	NA	NA	NA
WP_095660528.1\|2000426_2003165_-\|tRNA	valine--tRNA ligase	A0A1V0S951	Catovirus	6.6e-137	39.0
WP_095660529.1\|2003192_2004194_-	malate dehydrogenase	NA	NA	NA	NA
WP_095660530.1\|2004284_2005133_+	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_095660531.1\|2005137_2006415_-\|protease	ATP-dependent Clp protease ATP-binding subunit ClpX	G3M9Z9	Bacillus_virus	5.3e-137	59.0
WP_095660532.1\|2006560_2007334_+	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_157731342.1\|2007352_2007982_+	hypothetical protein	NA	NA	NA	NA
WP_095660534.1\|2008001_2008796_+	alpha/beta fold hydrolase	NA	NA	NA	NA
WP_095660535.1\|2008832_2009429_+	hypothetical protein	NA	NA	NA	NA
WP_095660536.1\|2009500_2010121_-\|protease	ATP-dependent Clp protease proteolytic subunit	A0A223W000	Agrobacterium_phage	1.1e-39	45.0
WP_095660537.1\|2010154_2010748_-\|protease	ATP-dependent Clp protease proteolytic subunit	A0A223W000	Agrobacterium_phage	3.0e-42	48.6

DBSCAN-SWA_2

2039674 : 2069988

Gordonia_phage(25.0%)

protease,transposase,integrase

attL 2039551:2039566|attR 2060842:2060857

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
2039551:2039566	attL	NA	NA	NA	NA
WP_095660563.1\|2039674_2040871_-\|transposase	IS481 family transposase	S5WIU1	Leptospira_phage	3.2e-11	27.0
WP_095658980.1\|2041231_2042581_-\|transposase	IS256 family transposase	A0A218MNI5	uncultured_virus	6.1e-35	36.6
WP_095660564.1\|2042889_2043540_-\|transposase	IS3 family transposase	A0A1B3AZE5	Gordonia_phage	5.0e-35	43.8
WP_157731348.1\|2043536_2043854_-\|transposase	transposase	A0A1B3AZF8	Gordonia_phage	4.5e-13	47.1
WP_095660567.1\|2046001_2046649_-	NAD(P)H-binding protein	NA	NA	NA	NA
WP_095660568.1\|2046667_2047579_-	EamA family transporter	NA	NA	NA	NA
WP_095661164.1\|2047563_2048505_-	pseudouridine-5'-phosphate glycosidase	NA	NA	NA	NA
WP_157731350.1\|2048497_2048728_-	hypothetical protein	NA	NA	NA	NA
WP_095660569.1\|2048768_2052593_-	AMP-binding protein	A0A2K9KZV5	Tupanvirus	4.9e-29	29.8
WP_095660570.1\|2052619_2053030_-	hypothetical protein	NA	NA	NA	NA
WP_157731307.1\|2052985_2053654_+	hypothetical protein	NA	NA	NA	NA
WP_095660330.1\|2053602_2054643_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	A0A2I6AZV9	Macacine_betaherpesvirus	2.8e-19	35.8
WP_095660572.1\|2054635_2055013_-	hypothetical protein	NA	NA	NA	NA
WP_095660573.1\|2055075_2055777_-	phosphoribosylanthranilate isomerase	NA	NA	NA	NA
WP_157731352.1\|2056533_2056680_+	hypothetical protein	NA	NA	NA	NA
WP_095660574.1\|2056682_2056967_+	hypothetical protein	NA	NA	NA	NA
WP_095660575.1\|2057122_2058505_+	MHS family MFS transporter	NA	NA	NA	NA
WP_095660576.1\|2058546_2058972_+	hypothetical protein	NA	NA	NA	NA
WP_095660577.1\|2058968_2059286_+	ArsR family transcriptional regulator	NA	NA	NA	NA
WP_095660578.1\|2059296_2060112_+	SDR family oxidoreductase	NA	NA	NA	NA
WP_095660579.1\|2060104_2060749_+	oligoribonuclease	Q8B5Y0	Diachasmimorpha_longicaudata_entomopoxvirus	1.1e-31	37.5
WP_095660580.1\|2060924_2062196_-	L,D-transpeptidase	NA	NA	NA	NA
2060842:2060857	attR	NA	NA	NA	NA
WP_095660581.1\|2062538_2063102_+	isochorismatase family protein	A0A2K9L2K0	Tupanvirus	8.5e-15	30.9
WP_095661165.1\|2063098_2063677_-	DUF305 domain-containing protein	NA	NA	NA	NA
WP_095660582.1\|2063841_2064117_-	DUF3618 domain-containing protein	NA	NA	NA	NA
WP_095660583.1\|2064205_2064676_+	thioredoxin-dependent thiol peroxidase	NA	NA	NA	NA
WP_095660584.1\|2065027_2065474_+	hypothetical protein	NA	NA	NA	NA
WP_095660585.1\|2065477_2065888_+	DUF3817 domain-containing protein	NA	NA	NA	NA
WP_095660586.1\|2065936_2066308_-	hypothetical protein	NA	NA	NA	NA
WP_095661166.1\|2066335_2066935_-	RdgB/HAM1 family non-canonical purine NTP pyrophosphatase	NA	NA	NA	NA
WP_095660587.1\|2066940_2067687_-	ribonuclease PH	NA	NA	NA	NA
WP_095660588.1\|2067702_2068473_-	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_095660589.1\|2068483_2069317_-	glutamate racemase	NA	NA	NA	NA
WP_095661167.1\|2069313_2069988_-\|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA

Anti-CRISPR protein detection

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

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP019688

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection