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_CP022436	Arthrobacter sp. YN chromosome, complete genome	3 crisprs	csa3,cas3,DinG,WYL,DEDDh	1	0	2	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP022436_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022436_1

1787369-1787466

Orphan

Consensus_repeat	Method
CGTCCGGGCAACAACCCGTTTGC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022436_1

>merge|NZ_CP022436|1|1787369-1787466|CRISPRCasFinder
CGTCCGGGCAACAACCCGTTTGCTACCTCCCAGGGCATGCCCCGGGGCCGTGGTGGCGACGGAGATCGTCCGCCGCGTCCGGGTAACAACCCGTTTGC

>NZ_CP022436|1|1|1787369-1787466|CRISPRCasFinder
CGTCCGGGCAACAACCCGTTTGC	TACCTCCCAGGGCATGCCCCGGGGCCGTGGTGGCGACGGAGATCGTCCGCCG
CGTCCGGGTAACAACCCGTTTGC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022436.1\|WP_089594382.1\|1795128_1795398_+\|30S-ribosomal-protein-S15	unknown	unknown	gnl\|CDD\|180170
NZ_CP022436.1\|WP_089594378.1\|1790445_1790928_+\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|238612
NZ_CP022436.1\|WP_089594369.1\|1779934_1780732_+\|TSUP-family-transporter	unknown	unknown	gnl\|CDD\|182593
NZ_CP022436.1\|WP_089594384.1\|1797978_1799322_+\|insulinase-family-protein	unknown	unknown	gnl\|CDD\|223685
NZ_CP022436.1\|WP_089594385.1\|1799400_1799862_+\|DUF1579-family-protein	unknown	unknown	gnl\|CDD\|377882
NZ_CP022436.1\|WP_089594372.1\|1783363_1784584_-\|DUF4439-domain-containing-protein	unknown	unknown	gnl\|CDD\|373114
NZ_CP022436.1\|WP_089594380.1\|1793450_1793897_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022436.1\|WP_089594367.1\|1776994_1777726_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022436.1\|WP_089594374.1\|1785225_1786206_+\|transcription-termination/antitermination-protein-NusA	unknown	unknown	gnl\|CDD\|237061
NZ_CP022436.1\|WP_089597287.1\|1792126_1793092_+\|tRNA-pseudouridine(55)-synthase-TruB	unknown	unknown	gnl\|CDD\|235113
NZ_CP022436.1\|WP_089594377.1\|1789857_1790361_+\|30S-ribosome-binding-factor-RbfA	unknown	unknown	gnl\|CDD\|234787
NZ_CP022436.1\|WP_089594368.1\|1778126_1779938_+\|proline--tRNA-ligase	unknown	unknown	gnl\|CDD\|236405
NZ_CP022436.1\|WP_089594375.1\|1786295_1786745_+\|YlxR-family-protein	unknown	unknown	gnl\|CDD\|377288
NZ_CP022436.1\|WP_089594371.1\|1781526_1782534_-\|aminoglycoside-resistance-protein	unknown	unknown	gnl\|CDD\|309685
NZ_CP022436.1\|WP_089597285.1\|1782583_1783312_-\|VIT-family-protein	unknown	unknown	gnl\|CDD\|153123
NZ_CP022436.1\|WP_089594383.1\|1795636_1797889_+\|polyribonucleotide-nucleotidyltransferase	unknown	unknown	gnl\|CDD\|131743
NZ_CP022436.1\|WP_089594379.1\|1793094_1793448_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022436.1\|WP_089594381.1\|1793985_1794969_+\|bifunctional-riboflavin-kinase/FAD-synthetase	unknown	unknown	gnl\|CDD\|235536
NZ_CP022436.1\|WP_089594373.1\|1784614_1785226_+\|ribosome-maturation-factor-RimP	unknown	unknown	gnl\|CDD\|234627
NZ_CP022436.1\|WP_089594370.1\|1780746_1781523_-\|DUF108-domain-containing-protein	unknown	unknown	gnl\|CDD\|224626

Protein	Function_ID	Function_description	E-value
NZ_CP022436.1\|WP_089594382.1\|1795128_1795398_+\|30S-ribosomal-protein-S15	gnl\|CDD\|180170	PRK05626, rpsO, 30S ribosomal protein S15; Reviewed.	1.18664e-53
NZ_CP022436.1\|WP_089594369.1\|1779934_1780732_+\|TSUP-family-transporter	gnl\|CDD\|182593	PRK10621, PRK10621, hypothetical protein; Provisional.	1.33052e-41
NZ_CP022436.1\|WP_089594384.1\|1797978_1799322_+\|insulinase-family-protein	gnl\|CDD\|223685	COG0612, PqqL, Predicted Zn-dependent peptidases [General function prediction only].	4.33736e-109
NZ_CP022436.1\|WP_089594385.1\|1799400_1799862_+\|DUF1579-family-protein	gnl\|CDD\|377882	pfam07617, DUF1579, Protein of unknown function (DUF1579). A family of paralogous hypothetical proteins identified in Rhodopirellula baltica that also has members in Gloeobacter violaceus, Sinorhizobium meliloti and Agrobacterium tumefaciens.	0.00310944
NZ_CP022436.1\|WP_089594372.1\|1783363_1784584_-\|DUF4439-domain-containing-protein	gnl\|CDD\|373114	pfam14530, DUF4439, Domain of unknown function (DUF4439). This domain has a ferritin-like fold.	1.19278e-20
NZ_CP022436.1\|WP_089594378.1\|1790445_1790928_+\|nucleoside-deaminase	gnl\|CDD\|238612	cd01285, nucleoside_deaminase, Nucleoside deaminases include adenosine, guanine and cytosine deaminases. These enzymes are Zn dependent and catalyze the deamination of nucleosides. The zinc ion in the active site plays a central role in the proposed catalytic mechanism, activating a water molecule to form a hydroxide ion that performs a nucleophilic attack on the substrate. The functional enzyme is a homodimer. Cytosine deaminase catalyzes the deamination of cytosine to uracil and ammonia and is a member of the pyrimidine salvage pathway. Cytosine deaminase is found in bacteria and fungi but is not present in mammals; for this reason, the enzyme is currently of interest for antimicrobial drug design and gene therapy applications against tumors. Some members of this family are tRNA-specific adenosine deaminases that generate inosine at the first position of their anticodon (position 34) of specific tRNAs; this modification is thought to enlarge the codon recognition capacity during protein synthesis. Other members of the family are guanine deaminases which deaminate guanine to xanthine as part of the utilization of guanine as a nitrogen source.	4.16267e-37
NZ_CP022436.1\|WP_089594374.1\|1785225_1786206_+\|transcription-termination/antitermination-protein-NusA	gnl\|CDD\|237061	PRK12327, nusA, transcription elongation factor NusA; Provisional.	0
NZ_CP022436.1\|WP_089597287.1\|1792126_1793092_+\|tRNA-pseudouridine(55)-synthase-TruB	gnl\|CDD\|235113	PRK03287, truB, tRNA pseudouridine synthase B; Provisional.	2.455e-163
NZ_CP022436.1\|WP_089594377.1\|1789857_1790361_+\|30S-ribosome-binding-factor-RbfA	gnl\|CDD\|234787	PRK00521, rbfA, 30S ribosome-binding factor RbfA.	2.06052e-46
NZ_CP022436.1\|WP_089594368.1\|1778126_1779938_+\|proline--tRNA-ligase	gnl\|CDD\|236405	PRK09194, PRK09194, prolyl-tRNA synthetase; Provisional.	0
NZ_CP022436.1\|WP_089594375.1\|1786295_1786745_+\|YlxR-family-protein	gnl\|CDD\|377288	pfam04296, DUF448, Protein of unknown function (DUF448).	4.7704e-22
NZ_CP022436.1\|WP_089594371.1\|1781526_1782534_-\|aminoglycoside-resistance-protein	gnl\|CDD\|309685	pfam04655, APH_6_hur, Aminoglycoside/hydroxyurea antibiotic resistance kinase. The aminoglycoside phosphotransferases achieve inactivation of their antibiotic substrates by phosphorylation utilising ATP. Likewise hydroxyurea is inactivated by phosphorylation of the hydroxy group in the hydroxylamine moiety.	2.17839e-22
NZ_CP022436.1\|WP_089597285.1\|1782583_1783312_-\|VIT-family-protein	gnl\|CDD\|153123	cd02432, Nodulin-21_like_1, Nodulin-21 and CCC1-related protein family. Nodulin-21_like_1: This is a family of proteins closely related to nodulin-21, a plant nodule-specific protein that may be involved in symbiotic nitrogen fixation. This family is also related to CCC1, a yeast vacuole transmembrane protein that functions as an iron and manganese transporter. .	5.38338e-97
NZ_CP022436.1\|WP_089594383.1\|1795636_1797889_+\|polyribonucleotide-nucleotidyltransferase	gnl\|CDD\|131743	TIGR02696, polyribonucleotide_nucleotidyltransferase, guanosine pentaphosphate synthetase I/polynucleotide phosphorylase. Sohlberg, et al. present characterization of two proteins from Streptomyces coelicolor. The protein in this family was shown to have poly(A) polymerase activity and may be responsible for polyadenylating RNA in this species. Reference 2 showed that a nearly identical plasmid-encoded protein from Streptomyces antibioticus is a bifunctional enzyme that acts also as a guanosine pentaphosphate synthetase.	0
NZ_CP022436.1\|WP_089594381.1\|1793985_1794969_+\|bifunctional-riboflavin-kinase/FAD-synthetase	gnl\|CDD\|235536	PRK05627, PRK05627, bifunctional riboflavin kinase/FAD synthetase.	5.42828e-125
NZ_CP022436.1\|WP_089594373.1\|1784614_1785226_+\|ribosome-maturation-factor-RimP	gnl\|CDD\|234627	PRK00092, PRK00092, ribosome maturation protein RimP; Reviewed.	6.32921e-37
NZ_CP022436.1\|WP_089594370.1\|1780746_1781523_-\|DUF108-domain-containing-protein	gnl\|CDD\|224626	COG1712, COG1712, Predicted dinucleotide-utilizing enzyme [General function prediction only].	4.34563e-47

>NZ_CP022436.1|WP_089594375.1|1786295_1786745_+|YlxR-family-protein
MEPGLRPVSARFGVPQLRVQDRGPSGASNVRQVGRVVAELLEHGHGPVRTCIGCRKQGSRSELVRLVTQGSGSSAVLVDVRRRMAGRGAWLHPSEKCLALAIKRRAFGRALAGAAETDAVERYLMQGTPLVEAQAATGKPSKPESGSEN
>NZ_CP022436.1|WP_089594374.1|1785225_1786206_+|transcription-termination/antitermination-protein-NusA
MDIDMSALRLLEREREIPLDLLIPTIEQALLVAYHKTPGAFEKARAELDRKSGHVTIWATEIDDDGEPIGEFEDTPAGFGRIAASTARQIILQRLRDVEDDNVLGEFKGREGELVAGMIQQGNNPHMIQVNLGAVEALLPPPEQVPGEKYLHGSRLRAFVVDVHRGAKGPSITLSRSHPGLVRKLFEMEVPEIADHSVEIVALAREAGHRTKIAVKANTPGINAKGACIGEMGSRVRAVMTELNDEKIDIVDFSDDPATFIANSLSPSRVNSVTITDESTRSARVVVPDYQLSLAIGKEGQNARLAAKLTGWRIDIVSDAAPAKVD
>NZ_CP022436.1|WP_089594373.1|1784614_1785226_+|ribosome-maturation-factor-RimP
MSDSEATTSTHRSESNSTATIHNPEESRLKALLEPAVLASRLYLEDVSIHVAGSHRTVHVVVDLPQEETGGVSLDAIADVSRGLSDILDNDPHDDGRPYDLEVSSPGVSRPLTEPRHWHRARGRMVRVNVIQGDNLLGRIASVEDDGVTLIPEHEVKKGMKPKQGDPITIPFDRIRQGKVEIEFSHLHEAALADEHNGPSEEA
>NZ_CP022436.1|WP_089594372.1|1783363_1784584_-|DUF4439-domain-containing-protein
MTTSLTIFPGTWCTDFATHVTPWSVVSGQTSEKRRTPPWGRVLLVAVVALLVAGTGIVLIPRDSGTPPPVPFSETARARALEDTLQLRGSAAALSSAAGQGAAQPALQDAVTLLTTQARALLVPSEATPSATATPAGTAETTTRAAFVAALSASGTQRLADAYEADGGIARLLAAVGSAQVLGAEKLAGAWQLPVPKDAAASKTKKPAATPSTAPCPSVSPTPEPTSATTDAALAATVRTHQEAVYAYQVALKRLDTGAAGTAAKGLATHELLLQQVEALTRANCGDVPASEAGYRLPGQFAQDPAAALAALESSALPVLGDLVALSTGETRAWAVDGLLAAGRRSLAWGADVPALPGLTLDAGELPPLPTPGSATGSATGSVSGSATTTPSTESTTNGSTPPPAG
>NZ_CP022436.1|WP_089597285.1|1782583_1783312_-|VIT-family-protein
MASPDTATVHENEPHRDDLAHRLNWLRAGVLGANDGIVSVAAIVVGVAGATTSTGSILAAGTAGLVGGAISMALGEYVSVSSQSDTQKALIEKERLELAQQPEDELNELAAIYESKGLSAKTARAVAEELTEHDALAAHLSAELNIHEDDIVSPWNAALASAVAFTLGAILPMLAILLPPPELRVPLTFVAVLLALAITGAVGAWIGGASRFRAAFRVVLGGALALAATFSLGTLLGASGVF
>NZ_CP022436.1|WP_089594371.1|1781526_1782534_-|aminoglycoside-resistance-protein
MIPIPGDLHARYNRDSAGRDWLASLPGLISDALDRWQLSVDLAPGTEPWNGHGALVVPVLQNGAPSALKIAYPHDEAQVERHALALWDGHGAVRLLAADAPTCTMLLERLDASRWLQDAPMDHARDAWGAVLRRLSIQPDERLEWQALEHIAATAERWSDELPAEWERLDRPFPRWLLEAALEVCQTRGAVGRRSGTDVLVHTDLHFMNILAVPSGNRQLRGDYLAIDPQPQVGEAEFAVAPVLWNRIHDLSRTAPEAALRERCHDFSVAAGLDPEAARQWSIAREVDNALGYAGTPGHGGDFARSLWVASTLAGRTLDDLPRAHELPVPGATAF
>NZ_CP022436.1|WP_089594370.1|1780746_1781523_-|DUF108-domain-containing-protein
MTLNVALIGSGAIGSRIVELLDAGTVPGVRLAGVVPHGNAGTGFSFDDALEVADVVVECAGVAAVAEFGPRTVAAGTDLLVTSIGALCDQSLRTKLLDDGPGRTFLTTGALGGLDAITAAGAGGTIHRITLESRKLPAALVQPWMDGETKEGLLAATRPVELLRGGPAELIKAFPKSTNVVSALALAAGSWEVVEAVLIADPGASRTAHHVVAETNLGTFDICVTNEASPGNPASSALVPHAVVRGLKSLANASGSFI
>NZ_CP022436.1|WP_089594369.1|1779934_1780732_+|TSUP-family-transporter
MISGFESIQLTTLILIVVAGFAAGWVDAVVGGGGLIQLPALLLVPGITPVQALATNKMGSIFGTTTSAVTYYRRVGPDLKTAVPMAVIALAGSFGGAILAASLPASVFKPIIVVALIAVAIFTALRPRAGELTALRHDGHKHYVVACLIGAVIGFYDGLIGPGTGSFLVIALVSAMGYAFLEASAKAKIVNMATNAGALIFFLPHGSLLWGVGLVLGLANMAGGYLGARTAVAKGSGFVRVVFLIVVAALIIKLGIDVWNENFAG
>NZ_CP022436.1|WP_089594368.1|1778126_1779938_+|proline--tRNA-ligase
MVLRLSQLFLRTLREDPVDAEVASHKLLVRAGYIRRAAPGIYTWLPLGLSVLRKVEEIIRQEMSAIGAQEVHFPALLPREPYEATNRWTEYGEGLFRLQDRKGADYLLAPTHEEMFTLLVKDLYSSYKDLPLSLYQIQNKYRDEARPRAGLLRGREFIMKDSYSFDIDDAGLDASYAAHRAAYLKIFERLGLEVIPVAATAGAMGGSKSEEFLFPTEIGEDTFVRSAGGYYANVEAVTTVVPDEIDFSNAPDAQVLDTPNTPTIETLVAAANQLAPRSEADGGAWTAADTLKNVVLAVTLPTGERQIVVIGVPGDRGVDLKRVEANIGSHLPIAGEIGLEAANEEDLKKLPWLVKGYIGPGLSLDQPVLGIEGSSKVLFLVDPRVVSGTSWVTGANAEGKHVFGLVAGRDFAWDGVIESTEVRAGDPAPDGSGPLETARGIEMGHIFQLGRKYAAALDLKVLDQNGKQQVVTMGSYGVGVTRAVAALAEANHDDRGLVWPRSVAPADVHVVAVGRGDEIFEAAEKLSAELEAAGLDVIFDDRPKVSPGVKFGDAELVGVPTILAVGRGLVDGVVEIKDRRSGEAENVAVDKAVDYVVNAVRNR
>NZ_CP022436.1|WP_089594367.1|1776994_1777726_+|hypothetical-protein
MKKNALRGFAVSGLLVMSLTACGGAGTSTDAASAPASETPAPAPAQAKQYTTQELTDLVKQIKAADGTELMVSSVDDLAGQQDPLKELLGSMNIEPAECKDLAMAGASQPIEGATGASGAKIDAASGVISSVTLASGVSKDVLENNVKSNEDQITTCANMTMSMSGTTMTMKTEKFDGIGSVPGTLGIKTTMTLPDGQTQSTLMAAAIKDGVLISATASGKNAENGGAAAAGALMDQAAALIK
>NZ_CP022436.1|WP_089594377.1|1789857_1790361_+|30S-ribosome-binding-factor-RbfA
MADPARAAKLAQRIKVVVAEALGRRVKDPRVESITVTDARVTNDLQHATIYYTVFGDEVAHADAARALEKAKGVLRQEVGRNITVRLTPTLEFVADQIPVNASNLEELLREAKRRDAEVAALAASAKHAGEADPYKGDAPEDIDEDDFDEEDTDLSGDKELDEDANR
>NZ_CP022436.1|WP_089594378.1|1790445_1790928_+|nucleoside-deaminase
MSAHTAQQRDDYLNRAIHLAVQNVSDGGGPFGAVVVTPDGTVHEGVNRVTRDHDPTAHAEVVAIRRAASATQRFDLTGSVLYASCEPCPLCLSAALWARIGHVYFAADRHGAARAGFDDAVFYEYFAGARPGLLPVEHAGLPASDDPFEAWLNHSRRTAY
>NZ_CP022436.1|WP_089597287.1|1792126_1793092_+|tRNA-pseudouridine(55)-synthase-TruB
MGAILATHILVSVLSGLVIVDKPQGWTSHDVVGRMRRLAGTRKVGHAGTLDPMATGVLVLGINKATRLLTYIVGTSKTYTATIRLGETTITDDAEGEVTESRTAAEVTDDAIAAGVAALTGPIQQVPSSVSAIKVNGERSYARVRSGEEVKLAARPVTIHRFDVHSITRVDGGRVVDVDVTVECSSGTYIRALARDLGNGLDVGGHLTALRRTQVGPYTLDQARTLEELAEELNVLEMSLAARALMPNRELSEEETTEISFGRRIAAGPGAGTPTAATAENPAAAFAPSGELVALLADAGSFAKPVLVFAPGTGPGTGQAH
>NZ_CP022436.1|WP_089594379.1|1793094_1793448_+|hypothetical-protein
MDGYFYAILIVGLVSTIMCLVAGLMKKAPNDPTIFSVLAVELVLLVYLVGSIVRVAMGEQIAGEAWEFWGYLVTALMIPLGAVYWAILERTRWSNFVLAAVGVTVLVMGARMNQIWY
>NZ_CP022436.1|WP_089594380.1|1793450_1793897_+|hypothetical-protein
MKEEHDVTGTETNPANPQQKDTRNTGPGRLLIAVYAVFALSATARAGYQIATKFAEAPLAHILSAFAAVVYIVATISLAKPGRTWFKVSLAAVLTELVGVLVVGAISLFDPVAFPHDTVWSLFGRGYGFVPLVLPILGLLWLNKRRPS
>NZ_CP022436.1|WP_089594381.1|1793985_1794969_+|bifunctional-riboflavin-kinase/FAD-synthetase
MVHIWNDPTEVPKDFGATVVTIGNFDGVHRGHQHVLAQLTDTAKRHNIPSVAVTFDPHPAQVHRPDSAPELIMGLQDKLEALADTGVDAVLVMKYTLDLAAMTPLEFVRGVLLDGLHAAHLVVGHDLRFGAGNAGDVVTMQELGDQLGFSVQVVNEYGAGGFPVHDDGDTDRRCSSTWVREALSEGDVVTAAAVLGRPHRMRGEVVHGAARGRDLGFPTANLSHDSTGYVPADGIYAGWLIDQSGTRWPAAISVGSNPTFDGVSRQVEAHVIDRPEENVEDFDLYGQTVAVEFTQRLRGMVAYRGPEALVEQMCLDVAQAHELLGQS
>NZ_CP022436.1|WP_089594382.1|1795128_1795398_+|30S-ribosomal-protein-S15
MALEAAVKQSIIKEYATSEGDTGSPEVQVAVLTQRIKDLTEHMKEHKHDFHTQRGLLAMVGRRKRMLSYLKNTDIARYRALIERLGLRR
>NZ_CP022436.1|WP_089594383.1|1795636_1797889_+|polyribonucleotide-nucleotidyltransferase
MEGPEIQFSEAIIDNGRFGKRVIRFETGRLAKQAAGASMVYIDEDTALLSATTAGKQPREGFDFFPLTVDVEERMYAAGRIPGSFFRREGRPSTEAILACRLMDRPLRPAFVKGLRNEVQIVVTVLAINPDELYDVVAINASSMSTQLSGLPFSGPIGGVRVALIADEQGSQWVAFPKHSQLENAVFNMVVAGRITGDDVAIMMVEAEATDNSWNLIKEQGATAPTEEVVSEGLEAAKPFIKALCEAQADLAARAAKPTVEFPVFLDYQDDVYAAVEAAAADKLAAVFQIADKQDRDTASDELKDEVLGALAGNFEGREKELSAAFRSVTKQVVRQRILKDQIRIDGRGLTDIRQLTAEVEVLPRVHGSAIFERGETQIMGVTTLNMLKMEQQIDSLSPVTRKRYMHNYNFPPYSTGETGRVGSPKRREIGHGALAERALVPVLPTREEFPYAIRQVSEALSSNGSTSMGSVCASTLSMLNAGVPLKAAVAGIAMGLVSDQVDGQTRYAALTDILGAEDAFGDMDFKVAGTSEFVTAIQLDTKLDGIPASVLAAALKQAREARLHILEVINAAIDTPDELSEFAPRVIAVKIPVDKIGEVIGPKGKMINQIQEDTGADISIEDDGTVYIGATNGPSADAARSAINAIANPQVPEIGERYLGTVVKTTTFGAFVSLTPGKDGLLHISELRKLANGKRVDNVDDVVSVGQKVQVEITKIDDRGKLSLSPVVAEEDGAVAEDAPAEAAEESAE
>NZ_CP022436.1|WP_089594384.1|1797978_1799322_+|insulinase-family-protein
MTVVPLPLEQTLPGGELIHGAEGGSVVRRSVLPGGVRVLTEAMPGQRSATIGFWVAVGSRDEADGQHGSTHFLEHLLFKGTKRRTALEIASAFDEVGGESNAATAKESTCYFARVLDTDLPMAIDVIADMITGAVLDPAELEQERDVILEEIAMDSDDPTDVAHEKFVEAVLGHHPLARPIGGTPDAIKAVARDAVWAHYQRYYRPEELVITAAGGLDHDVVCDLVLDALTAAGWNLDPQAAPVNRRGTDRAVISGTSGLHVVKRPVEQANIIMGCPTIVATDDRRFVMSVLNAVLGGGMSSRLFQEIREKRGLVYSTYSFTAAYADAGYFGMYAGCTPSKVRQVLDLLGVELEKLAKEGITEEELRKAVGQLSGGIVLALEDTGSRMSRLGRAELVSGEFQDIDETLARIQAVTVEEVQDLARELAAAPRTITVVGPFEETETFGL
>NZ_CP022436.1|WP_089594385.1|1799400_1799862_+|DUF1579-family-protein
MDLPSSGQAAELLQDFIGHWLGITEIAASPWGSARTAEAEVVFTKAAGGYAVVQSYRHREADGTHFEGHGMFTVDRDHGDTLWYYVDSLGRSPASPVRGAWNAGTLTLDRRTADGVARHTFRVEDGVLVHTADLRLEGTPDFSPLLKSVFRKA

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Crispr_ID: NZ_CP022436_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022436_2

3608177-3608314

Orphan

Consensus_repeat	Method
CAGACCCACGCTCTCTCACATCCCGCGCCCTTCAGACCCAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022436_2

>merge|NZ_CP022436|2|3608177-3608314|CRISPRCasFinder
CAGACCCACGCTCTCTCACATCCCGCGCCCTTCAGACCCACGCTCTCTCACATCCCGCGCCCTTCCAGACCCACCGTCTCTCACATCCCGCGCCCTTCAGACCCACGCTCTCTCACATCCCGCGCCCTTCCAGACCCA

>NZ_CP022436|2|2|3608177-3608314|CRISPRCasFinder
CAGACCCACGCTCTCTCACATCCCGCGCCCTTCAGACCCAC	GCTCTCTCACATCCCGCGCCCTTCCAGACCCACCGTCTCTCACATCCCGCGCCCTT
CAGACCCACGCTCTCTCACATCCCGCGCCCTTCCAGACCCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022436.1\|WP_089595770.1\|3612677_3614990_-\|malto-oligosyltrehalose-synthase	unknown	unknown	gnl\|CDD\|237740
NZ_CP022436.1\|WP_089597529.1\|3617335_3618835_-\|NAD(P)H-hydrate-epimerase	unknown	unknown	gnl\|CDD\|238576
NZ_CP022436.1\|WP_089595766.1\|3606462_3608151_+\|formate--tetrahydrofolate-ligase	unknown	unknown	gnl\|CDD\|237403
NZ_CP022436.1\|WP_089595759.1\|3599314_3599986_-\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB	unknown	unknown	gnl\|CDD\|274750
NZ_CP022436.1\|WP_089595764.1\|3604463_3604982_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP022436.1\|WP_089595771.1\|3614986_3617266_-\|glycogen-debranching-protein-GlgX	unknown	unknown	gnl\|CDD\|131155
NZ_CP022436.1\|WP_089595772.1\|3619282_3621166_-\|glutamine--fructose-6-phosphate-transaminase-(isomerizing)	unknown	unknown	gnl\|CDD\|234729
NZ_CP022436.1\|WP_089595773.1\|3623214_3624579_-\|phosphoglucosamine-mutase	unknown	unknown	gnl\|CDD\|237672
NZ_CP022436.1\|WP_089595763.1\|3603088_3604483_+\|6-phospho-beta-glucosidase	unknown	unknown	gnl\|CDD\|133432
NZ_CP022436.1\|WP_089595760.1\|3599985_3600570_-\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-ATPase-subunit-type-1-TsaE	unknown	unknown	gnl\|CDD\|376771
NZ_CP022436.1\|WP_089595768.1\|3609730_3610768_-\|L-glyceraldehyde-3-phosphate-reductase	unknown	unknown	gnl\|CDD\|381377
NZ_CP022436.1\|WP_089595757.1\|3597646_3598807_-\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-transferase-subunit-TsaD	unknown	unknown	gnl\|CDD\|236585
NZ_CP022436.1\|WP_011775548.1\|3618930_3619278_-\|holo-ACP-synthase	unknown	unknown	gnl\|CDD\|234610
NZ_CP022436.1\|WP_089597531.1\|3622343_3623147_+\|M15-family-metallopeptidase	unknown	unknown	gnl\|CDD\|350624
NZ_CP022436.1\|WP_089595769.1\|3610849_3612619_-\|malto-oligosyltrehalose-trehalohydrolase	unknown	unknown	gnl\|CDD\|274114
NZ_CP022436.1\|WP_089595758.1\|3598803_3599301_-\|ribosomal-protein-S18-alanine-N-acetyltransferase	unknown	unknown	gnl\|CDD\|273701
NZ_CP022436.1\|WP_089595765.1\|3605114_3606359_+\|D-inositol-3-phosphate-glycosyltransferase	unknown	unknown	gnl\|CDD\|132490
NZ_CP022436.1\|WP_089595761.1\|3600566_3601820_-\|alanine-racemase	unknown	unknown	gnl\|CDD\|143481
NZ_CP022436.1\|WP_157731855.1\|3601928_3603059_-\|carbohydrate-kinase-family-protein	unknown	unknown	gnl\|CDD\|238917
NZ_CP022436.1\|WP_089595767.1\|3608473_3609559_-\|inositol-3-phosphate-synthase	unknown	unknown	gnl\|CDD\|132491

Protein	Function_ID	Function_description	E-value
NZ_CP022436.1\|WP_089595770.1\|3612677_3614990_-\|malto-oligosyltrehalose-synthase	gnl\|CDD\|237740	PRK14511, PRK14511, malto-oligosyltrehalose synthase.	0
NZ_CP022436.1\|WP_089597529.1\|3617335_3618835_-\|NAD(P)H-hydrate-epimerase	gnl\|CDD\|238576	cd01171, YXKO-related, B.subtilis YXKO protein of unknown function and related proteins. Based on the conservation of the ATP binding site, the substrate binding site and the Mg2+binding site and structural homology this group is a member of the ribokinase-like superfamily.	1.33051e-54
NZ_CP022436.1\|WP_089595766.1\|3606462_3608151_+\|formate--tetrahydrofolate-ligase	gnl\|CDD\|237403	PRK13505, PRK13505, formate--tetrahydrofolate ligase; Provisional.	0
NZ_CP022436.1\|WP_089595759.1\|3599314_3599986_-\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB	gnl\|CDD\|274750	TIGR03725, T6A_YeaZ, tRNA threonylcarbamoyl adenosine modification protein YeaZ. This family describes a protein family, YeaZ, now associated with the threonylcarbamoyl adenosine (t6A) tRNA modification. Members of this family may occur as fusions with ygjD (previously gcp) or the ribosomal protein N-acetyltransferase rimI, and is frequently encoded next to rimI. [Protein synthesis, tRNA and rRNA base modification].	1.08112e-52
NZ_CP022436.1\|WP_089595764.1\|3604463_3604982_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	4.7641e-08
NZ_CP022436.1\|WP_089595771.1\|3614986_3617266_-\|glycogen-debranching-protein-GlgX	gnl\|CDD\|131155	TIGR02100, Glycogen_operon_protein_GlgX_homolog, glycogen debranching enzyme GlgX. This family consists of the GlgX protein from the E. coli glycogen operon and probable equivalogs from other prokaryotic species. GlgX is not required for glycogen biosynthesis, but instead acts as a debranching enzyme for glycogen catabolism. This model distinguishes GlgX from pullanases and other related proteins that also operate on alpha-1,6-glycosidic linkages. In the wide band between the trusted and noise cutoffs are functionally similar enzymes, mostly from plants, that act similarly but usually are termed isoamylase. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP022436.1\|WP_089595772.1\|3619282_3621166_-\|glutamine--fructose-6-phosphate-transaminase-(isomerizing)	gnl\|CDD\|234729	PRK00331, PRK00331, isomerizing glutamine--fructose-6-phosphate transaminase.	0
NZ_CP022436.1\|WP_089595773.1\|3623214_3624579_-\|phosphoglucosamine-mutase	gnl\|CDD\|237672	PRK14318, glmM, phosphoglucosamine mutase; Provisional.	0
NZ_CP022436.1\|WP_089595763.1\|3603088_3604483_+\|6-phospho-beta-glucosidase	gnl\|CDD\|133432	cd05296, GH4_P_beta_glucosidase, Glycoside Hydrolases Family 4; Phospho-beta-glucosidase. Some bacteria simultaneously translocate and phosphorylate disaccharides via the phosphoenolpyruvate-dependent phosphotransferase system (PEP-PTS). After translocation, these phospho-disaccharides may be hydrolyzed by the GH4 glycoside hydrolases such as the phospho-beta-glucosidases. Other organisms (such as archaea and Thermotoga maritima ) lack the PEP-PTS system, but have several enzymes normally associated with the PEP-PTS operon. The 6-phospho-beta-glucosidase from Thermotoga maritima hydrolylzes cellobiose 6-phosphate (6P) into glucose-6P and glucose, in an NAD+ and Mn2+ dependent fashion. The Escherichia coli 6-phospho-beta-glucosidase (also called celF) hydrolyzes a variety of phospho-beta-glucosides including cellobiose-6P, salicin-6P, arbutin-6P, and gentobiose-6P. Phospho-beta-glucosidases are part of the NAD(P)-binding Rossmann fold superfamily, which includes a wide variety of protein families including the NAD(P)-binding domains of alcohol dehydrogenases, tyrosine-dependent oxidoreductases, glyceraldehyde-3-phosphate dehydrogenases, formate/glycerate dehydrogenases, siroheme synthases, 6-phosphogluconate dehydrogenases, aminoacid dehydrogenases, repressor rex, and NAD-binding potassium channel domains, among others.	1.46188e-180
NZ_CP022436.1\|WP_089595760.1\|3599985_3600570_-\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-ATPase-subunit-type-1-TsaE	gnl\|CDD\|376771	pfam02367, TsaE, Threonylcarbamoyl adenosine biosynthesis protein TsaE. This family of proteins is involved in the synthesis of threonylcarbamoyl adenosine (t(6)A).	7.73654e-42
NZ_CP022436.1\|WP_089595768.1\|3609730_3610768_-\|L-glyceraldehyde-3-phosphate-reductase	gnl\|CDD\|381377	cd19151, AKR_AKR14A2, Salmonella enterica aldo-keto reductase (AKR) and similar protein. Salmonella enterica AKR is a founding member of aldo-keto reductase family 14 member A2 (AKR14A2).	0
NZ_CP022436.1\|WP_089595757.1\|3597646_3598807_-\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-transferase-subunit-TsaD	gnl\|CDD\|236585	PRK09604, PRK09604, tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex transferase subunit TsaD.	7.59483e-171
NZ_CP022436.1\|WP_011775548.1\|3618930_3619278_-\|holo-ACP-synthase	gnl\|CDD\|234610	PRK00070, acpS, 4'-phosphopantetheinyl transferase; Provisional.	1.29921e-47
NZ_CP022436.1\|WP_089597531.1\|3622343_3623147_+\|M15-family-metallopeptidase	gnl\|CDD\|350624	cd14852, LD-carboxypeptidase, L,D-carboxypeptidase DacB and LdcB, and related proteins. This L,D-carboxypeptidase family includes LdcB LD-Carboxypeptidase from Streptococcus pneumoniae, Bacillus anthracis, and Bacillus subtilis, and L,D-carboxypeptidase DacB from Streptococcus pneumonia and Lactococcus lactis. These enzymes are active against cell-wall-derived tetrapeptides and synthetic tetrapeptides lacking the sugar moiety but are inactive against tetrapeptides terminating in L-alanine. L,D-carboxypeptidase DacB plays a key role in the remodeling of S. pneumoniae peptidoglycan during cell division. It adopts a zinc-dependent carboxypeptidase fold and acts as an L,D-carboxypeptidase towards the tetrapeptide L-Ala-D-iGln-L-Lys-D-Ala of the peptidoglycan stem. This family also includes vanY D-Ala-D-Ala carboxypeptidase which is vancomycin-inducible and penicillin-resistant. VanY hydrolyzes depsipeptide- and D-alanyl-D-alanine-containing peptidoglycan precursors; it is insensitive to beta-lactams. All these enzymes belong to the MEROPS family M15 subfamily B.	1.75069e-65
NZ_CP022436.1\|WP_089595769.1\|3610849_3612619_-\|malto-oligosyltrehalose-trehalohydrolase	gnl\|CDD\|274114	TIGR02402, Malto-oligosyltrehalose_trehalohydrolase, malto-oligosyltrehalose trehalohydrolase. Members of this family are the trehalose biosynthetic enzyme malto-oligosyltrehalose trehalohydrolase, formally known as 4-alpha-D-{(1->4)-alpha-D-glucano}trehalose trehalohydrolase (EC 3.2.1.141). It is the TreZ protein of the TreYZ pathway for trehalose biosynthesis, and alternative to the OtsAB system. [Energy metabolism, Biosynthesis and degradation of polysaccharides].	0
NZ_CP022436.1\|WP_089595758.1\|3598803_3599301_-\|ribosomal-protein-S18-alanine-N-acetyltransferase	gnl\|CDD\|273701	TIGR01575, rimI, ribosomal-protein-alanine acetyltransferase. Members of this model belong to the GCN5-related N-acetyltransferase (GNAT) superfamily. This model covers prokarotes and the archaea. The seed contains a characterized accession for Gram negative E. coli. An untraceable characterized accession (PIR\|S66013) for Gram positive B. subtilis scores well (205.0) in the full alignment. Characterized members are lacking in the archaea. Noise cutoff (72.4) was set to exclude M. loti paralog of rimI. Trusted cutoff (80.0) was set at next highest scoring member in the mini-database. [Protein synthesis, Ribosomal proteins: synthesis and modification].	9.11274e-33
NZ_CP022436.1\|WP_089595765.1\|3605114_3606359_+\|D-inositol-3-phosphate-glycosyltransferase	gnl\|CDD\|132490	TIGR03449, mycothiol_MshA, D-inositol-3-phosphate glycosyltransferase. Members of this protein family, found exclusively in the Actinobacteria, are MshA, the glycosyltransferase of mycothiol biosynthesis. Mycothiol replaces glutathione in these species.	1.86116e-166
NZ_CP022436.1\|WP_089595761.1\|3600566_3601820_-\|alanine-racemase	gnl\|CDD\|143481	cd00430, PLPDE_III_AR, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzyme Alanine Racemase. This family includes predominantly bacterial alanine racemases (AR), some serine racemases (SerRac), and putative bifunctional enzymes containing N-terminal UDP-N-acetylmuramoyl-tripeptide:D-alanyl-D-alanine ligase (murF) and C-terminal AR domains. These proteins are fold type III PLP-dependent enzymes that play essential roles in peptidoglycan biosynthesis. AR catalyzes the interconversion between L- and D-alanine, which is an essential component of the peptidoglycan layer of bacterial cell walls. SerRac converts L-serine into its D-enantiomer (D-serine) for peptidoglycan synthesis. murF catalyzes the addition of D-Ala-D-Ala to UDPMurNAc-tripeptide, the final step in the synthesis of the cytoplasmic precursor of bacterial cell wall peptidoglycan. Members of this family contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain. They exist as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. AR and other members of this family require dimer formation and the presence of the PLP cofactor for catalytic activity. Fungal ARs and eukaryotic serine racemases, which are fold types I and II PLP-dependent enzymes respectively, are excluded from this family.	1.07611e-145
NZ_CP022436.1\|WP_157731855.1\|3601928_3603059_-\|carbohydrate-kinase-family-protein	gnl\|CDD\|238917	cd01942, ribokinase_group_A, Ribokinase-like subgroup A. Found in bacteria and archaea, this subgroup is part of the ribokinase/pfkB superfamily. Its oligomerization state is unknown at this time.	1.6695e-59
NZ_CP022436.1\|WP_089595767.1\|3608473_3609559_-\|inositol-3-phosphate-synthase	gnl\|CDD\|132491	TIGR03450, mycothiol_INO1, inositol 1-phosphate synthase, Actinobacterial type. This enzyme, inositol 1-phosphate synthase as found in Actinobacteria, produces an essential precursor for several different products, including mycothiol, which is a glutathione analog, and phosphatidylinositol, which is a phospholipid.	0

>NZ_CP022436.1|WP_089595766.1|3606462_3608151_+|formate--tetrahydrofolate-ligase
MSENKVMSDLEIARNATILPIVDIAQRAGITVDALELYGPYKAKINPAKLVLPARTAPGKVVLVSAMSPTPAGEGKSTTTVGLADSLARAGHKVMIALREPSLGPILGMKGGATGGGYSQVLPMDDINLHFTGDFHAITSANNALMALVDNHIFQGNELGIDPRRIAFKRVLDMNDRSLREVVIGLGGPVQGVPRQDGFDITVASEIMAVFCLATDLDDLRSRLGRITFGYTYDRAPVTVADLGVEGALTMLLKDAIKPNLVQTIAGTPAVVHGGPFANIAHGCNSLIATSTAMQLADIVVTEAGFGADLGAEKYMDIKARIAAVAPSAVVVVATIRALKMQGGVPKDQLSQPNVEAMAAGVENLRRHVRNVAKFGISPIVSINKFATDTSAELEWLLAWCAAEGVEAAVADVWGRGGGGDGGDDLAAKVAAALDAPSDFHHLYPLEIPVEDKIRTIVQEIYGADGVEFSVPALKRLAEIEKNGWSDFPVCMAKTQYSFTDDASRLGAPKGFTVHVRELIPKTGAGFIVALTGAVMTMPGLPKEPAAMRMDVDAEGQPTGLF
>NZ_CP022436.1|WP_089595765.1|3605114_3606359_+|D-inositol-3-phosphate-glycosyltransferase
MPLIRRVAFLSLHTSPMEQPGAGDAGGMNVYVRALAMALAESGVEVEIFTRSTKAGQPAVEHPGPGVCVHNVMAGPRRKLPKEELPALLHQMVEEIDRIRGSQLHGRYDAIHSHYWVSGVAGLELSQLWGVPLVHTMHTMAKVKNLVLESGERPEPRRREEGEQRIVDGAARLVANTPAEAEELVSHYGADLDRIDVAPPGVDLKVFTPSFRRKSRSLRDVRPDSFHILFAGRIQRLKGPQVFVKAAGILRKRRPDIDLEMTILGSLSGAKDFNLQHIIEDAGLADVVTHRPPVVAPELASWFRSADVVVMPSFSESFGLVALEAQACGTPVVATNVGGLSRAISDGRTGMLVDGHDPSDWADALEDLYDDVQTREDMGRLAATHAESFGWQRTAAITLESYREAVGGLLVPRR
>NZ_CP022436.1|WP_089595764.1|3604463_3604982_-|GNAT-family-N-acetyltransferase
MAAVSQEQTFDIRKATPEDWPGIWAILEPVIRDGETFTWDRDTSEETARDKWTKDAPGQTFVAVGKDTGQILGTGEFHANQAGGGSHIANAGYMVGANNSGQGIARALCAYSLSEAKAAGFYAMQYNAVVESNVRAVWLWQSMGFRILATVPEAFDHPEIGYVGLHVMYRKL
>NZ_CP022436.1|WP_089595763.1|3603088_3604483_+|6-phospho-beta-glucosidase
MRLMIAGGGGFRVPLVYRALCAGPFAGLVDELVLYDVDAARLAAIEAVIGDMPPAGGSTPVVVVSTDLREALTGADMVFAAIRPGGTAGRIADERVALDLGLLGQETTGAGGISYALRSIPRMLELARAMRRHCPEAWLINFTNPAGMVTEALEPVLGRKVIGICDSAGGLVQRAARAVGAPLTEGTLDGVGYFGLNHLGWLYRLAPGGQDLLPGLLSDHAALESMEEGRLFGQHTLLQLGCLPNEYLYYYYQTAQATDAIRRQQETRGASIHHQQSALYPALAKAPHAFELWDSARRSREEGYLAEARTHGEQRDESDLAGGGYERVALSVMRALSGGGSAQLILNVPNSPVSAVGLATADVAVPGLPADAVVEVPCEVTPDGALPLTQARPGGQFLTLMQHVKEVERLTIRAVVHGERSAAVGAFAAHPLIGSAELGEQLLTGYEAAFPDLGQLWGPTASDT
>NZ_CP022436.1|WP_157731855.1|3601928_3603059_-|carbohydrate-kinase-family-protein
MQPSTVQRSLRCMDAMPQRRFDPLASLRSTADQQCDLLLTGTVFQDIIFTGLPHSPEPGTEIWSEGMGSCPGGVANQAIAAARLGLRTNLAATFGDDGYGDYNWQILESQEHVDLSLSRKVPGWHSPVTVSLCVNQDRSMVTHGHPAPISSSELIGQPPKALAAVADLGEELEPWMLAAKEGGTKLFGVVGWDPTGEWSERRLDLLENFHAFLPNAPEAMAFTGKADPWAALYSLADRVPVAVVTLGPQGAVALDSETGEEEWVPSLPVSAYDPTGAGDCFGAAFIVGCLAGWRLGDRLRFANLCASLAVQEVGGSLAAPGWGDIADWWQRANARKERQSSQWLRRFAFLEPIVKDIPAEAQRRARATIAHLSDAQ
>NZ_CP022436.1|WP_089595761.1|3600566_3601820_-|alanine-racemase
MTYEAAAEIGIGSKASIAKSAVLERSAVIDLEAVRHNVRQFVAIASPATVMAVVKADAYGHGAVQVARAALDAGAAWLGVAHISEALALRAAGVDAPLLAWLHTRESNFQAAVAAGIDVGISGWELDAVVAAAREQERPARVHLKVDTGLGRNGCPIADWDQLVGQAMEYQDQGLLRVVGIFSHLAVADEPHRPETDEQLAVFREAIAMAEDAGVDMEVRHIANTPATLSRPDSHFDLVRVGLGIYGLSPFEGATSAELGLHPAMTVRTLLSNCKKVPEGQGVSYGLNYRTSGESTLGLVPLGYADGVPRIGTGGPVRVNGTNYPVVGRIAMDQMVIDLGALTSDEAAAFKGAEAVMLGDGADGGPTADDWAAAAGTNNYEIVTRISPRVPRTYINEVPAQAEAHKAAGHATETAAL
>NZ_CP022436.1|WP_089595760.1|3599985_3600570_-|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-ATPase-subunit-type-1-TsaE
MSEPQWERTLTVTTAEQTHALAAAVGGVLEAGDLLVLTGELGAGKTTFTQGLGEGLGVRAGIISPTFVLVRIHPNLADGPRPGGPDLVHVDAYRLESAAEIDDIDLENTMDTAVTVVEWGRDRVEHLSDSRLEVDLHRSVGGESPATDAAAAGDVMDFDTDDDDEPRTLVFRGYGPRWAEVPRLLETPSPEKGN
>NZ_CP022436.1|WP_089595759.1|3599314_3599986_-|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB
MLILAIDTSAVASAALISDDAMESVVDSFATEDTRSHAEVLAPGIEKLLAGAGVTGTDIDAIVTGVGPGPFTGLRSGIATARTLAFVWNKPLYGLMSLDAIALEVAESTSAAPEFLVATDARRKEVYWARYTLADGQLPELVDGPHVGFASGLPDLPVFGAGAGLYAEVLNANEDFAQTQPDAASLGQFALAKLTAGQALLDSTPLYLRESDAQVPGPRKRAL
>NZ_CP022436.1|WP_089595758.1|3598803_3599301_-|ribosomal-protein-S18-alanine-N-acetyltransferase
MKLSPKLELAGVSLRDMTEADIPAVETLERRLFPVDAWPLQMFFDELAQPETRRYVVAEVAGEIVAYAGLMCIEPIADVQTIAVVPEFEGKGIGSAVLTELIDEARRRRAADVLLEVRADNPRAQQLYVRFGFEQIHVRPRYYRDGTDALIMRLELNKPHEGDTA
>NZ_CP022436.1|WP_089595757.1|3597646_3598807_-|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-transferase-subunit-TsaD
MSGAHPEQPKQPLVLGIESSCDETGVGIVRGTTLLTNTVSSSMEEHVRFGGVIPEIASRAHLDAFVPTLQESLHEAGVTLDDLDAIAVTSGPGLAGALMVGVCAAKALAVATGKPLYAINHLVAHVGVGLLDRQPASNGKAADGKHDAGAAAGLGAGKLPENLGALLVSGGHTEILRIRSITDDVELLGSTIDDAAGEAYDKVARILGLGYPGGPAIDKLARHGNPKSIRFPRGLSQPKYMGTAEEKGPHRYDWSFSGLKTAVARCVEQFEARGEEVPVSDIAAAFQEAVVDVISSKAVLACKEHGITDVLLGGGVAANSRLRELTGQRCASAGITLHVPPLDLCTDNGAMVAALGAQLIMAGIGPSGIAFAPDSSMPVTTVSVPA
>NZ_CP022436.1|WP_089595767.1|3608473_3609559_-|inositol-3-phosphate-synthase
MSSHPIRVAIVGVGNCAASLVQGVQYYRDADPKATIPGLMHVEFGQYHVNDVQFVAAFDVDSKKVGLDLADAIGASENNTIKIADVPTTGVTVQRGHTLDGLGKYYRETIVEAPDETVDIVAALREAKADVMVCYLPVGSDQAAKFYAQCAIDAGVAFVNALPVFIAGTKEWADKFTEAGVPIVGDDIKSQIGATITHRVMAKLFEDRGVTLDRTYQLNVGGNMDFKNMLERDRLESKKISKTQAVTSNVEAKLHADDVHIGPSDYVAWLDDRKWAFVRLEGRNFGDAPVSLEYKLEVWDSPNSAGVIIDAIRAAKIGLDRGIGGPLLSASSYFMKSPPEQFNDDLARDKVEAFIRGDIER
>NZ_CP022436.1|WP_089595768.1|3609730_3610768_-|L-glyceraldehyde-3-phosphate-reductase
MTYSAAENRYETMPYRRVGRSGLKLPAISLGLWHNFGDDKRFDEQRAILRRAFDLGVNHFDLANNYGPPDGSAETNFGRHLKDDFKPYRDELVISTKAGYYMWPGPYGEWGSRKYLISSLDQSLERMGLDYVDIFYSHRPDPETPLEETMGALDYAVRSGKALYAGISSYTPEQTLEAARILKELGTPLLIHQPSYSMLNRWTENGSPNLYEALDQVGAGSIAFSPLAQGMLTNRYLNGVPADSRAAKERFLSESQLTEEKLDRVRGLNAIAEGRGQTLAQMAIAWILRDQPKGSPVTSALVGASSVAQLEDTLSAINNLKFTTDELTAIDEFAVESDINRWAQK
>NZ_CP022436.1|WP_089595769.1|3610849_3612619_-|malto-oligosyltrehalose-trehalohydrolase
MLEHAAGKNRYDVWAPNADSVRLVADGREYAMEHHDAAAPGWWRAPADVVGQESDGVPYGYIVDGEGPFPDPRSRRQPDGVHALSATFDPSIHEWQDSAWKGRQLKGAVIYELHLGTFTPEGTLDAAAAKLDYLVDLGVDFIELLPVNGFNGVHNWGYDGVLWYAVHEPYGGPAAYQRFVDAAHAAGLGVIQDVVYNHLGPSGNYLPKFGPYLKSGEGNTWGDSVNLDGPGSDDVRRYILENAAMWLRDYHVDGLRLDAVHALRDERAVQILEEFGALGDQIEAETGIPRTLIAESDLNNPRLIYPRKDNGYGLDGQWSDDFHHAVHVNLSGETTGYYSDFDSLAVLAKVLEHGFLHDGSYSSFRGRHHGRPIRRDLAHPSALVVCLQNHDQIGNRAIGDRLTASLSYGQLAIGAVLTMTSPFTPMLFMGEEFGASTPWQFFTSHPEPELGKATAEGRIKEFERMGWDPAVVPDPQDPETFLRSKLKWEEVGEGKHASLLQLYKDLAQLRRNTPELVDGGFGSTVVEYDDDEHWLQFSRGTVRVVCNFGDEALGTPLSGSILLATDHEAVLDEGTLTLPGGSAVVARVN
>NZ_CP022436.1|WP_089595770.1|3612677_3614990_-|malto-oligosyltrehalose-synthase
MRTPVSTYRLQIRPGLTLQDAAELTGYLRTLGVDWVYVSPILTAEEGSDHGYDVTDPSTVDPSRGGPEGLSALSKAAREQGLGVLADIVPNHMGVASAGQNAWWWQLLKEGRGSKYAEAFDVDWDFGGGKIRIPVLGSDEDLEQITVVDGELHYYDHRFPLAEGTFAPGDSPQDVHARQHYQLIGWRRADAELNYRRFFAVNTLAGVRVEIPWVFDESHEEIVRWFREELVDGLRIDHPDGLADPEGYLARLREATGGAYLLVEKILEPGEQLPGTFSCEGTTGYDALADVDRLFVDPAAEEYLDSLDARLRDADAPADYEDMIHGTKRRIADGILRSEILRLARLVPQSMDLPADKVADAIAEVICCFPIYRTYLPYGQDVLEESIRRAAENRADLKAVLEDLRPLLLDSSGALARRFQQTSGMVMAKGVEDTAFFRYTRLGTLTEVGADPTEFAVSSGVFHERTARRQQVLPLSMTTLSTHDTKRSEDARARISVISEAVPEWELFLGTVQELAPIPDGPLAALVWQSIVGAWPADRGRLQSYALKAAREAGNSTNWTDPNQDFERHLAAAVDSVFDVPEVAAALANFVAELEPYGTSNSLSAKLVQLTMPGVPDVYQGTEFRDGSLTDPDNRRPVDFQARMTALAELDNGAAPPFTDEAAKLLVVSRALRLRRDRPELFGGYLPVVAQGAAADHVVAFDRGADRRGALTVATRLPKRLAREGGWRDTAIELSGNARDELTGATYSAGTVHLATLLEQYPVALLVPTD
>NZ_CP022436.1|WP_089595771.1|3614986_3617266_-|glycogen-debranching-protein-GlgX
MEVWPGSAYPLGATFDGTGTNFALFSEKAEKVELCLFDDDGGEVRVEVTEVDGYVWHCYLPQVQPGQKYGYRVHGPYDPDAGQRFNPNKLLLDPYAKAIHRQIDWDPALFSYNLGDPDSRNDEDSAPHMMLGVVINPFFDWDGDKLLRIPYHKSVIYEAHVKGLTQMHPEVPEEQRGTYAGVAHPAVISHLQKLGITAIELMPVHQFVNDGILQDKGLNNYWGYNTIGFFAPHNSYSSKGDTGQQVQDFKAMVRALHTAGIEVILDVVYNHTAEGNHLGPTLSFKGIDNSAYYRLVEDDQKYYMDYTGTGNSLNVRSPHSLQLLMDSLRYWVTEMHVDGFRFDLASTLAREFYDVDKLSTFFELIQQDPVVSQVKLIAEPWDVGPGGYQVGNFPPQWTEWNGQYRDTVRDFWRGEPSTLGEFASRLTGSADLYEHSGRRPVASINFVTAHDGFTLADLVSYNEKHNEANGEDNNDGESHNRSWNCGTEGPTEDPTVLGLRARQQRNFIATLFLSQGVPMLLHGDELGRTQRGNNNGYCQDSELTWINWENVDQPLIEFTAAVCALRAKHPSLRRSRFFDGRPVLRGEGERLPDIVWLDADASTMSPSDWDEALGRSVGVFLNGDGIHGRDNQGRRITDVNFLLYFNADQDEVGFRIPSDEYAPAWDVMIDTAGEGAEAGVVKPDQILMVGAKSLVVLRAHSTPEVEPDHSVAASLAALTQTSTPETASITAPAVTSLPFDYKGDAPAGEESGATKKADS
>NZ_CP022436.1|WP_089597529.1|3617335_3618835_-|NAD(P)H-hydrate-epimerase
MQRAAYGLAQAVVLEVKTRRKLAGASVTVLAGKGNNGGDGLFAAALLARRGMRTTAVLAAAEVHPEALAAFAAAGGRTFYLEPGNAEELAVLCAGDDVIIDALLGTGARGGLRGPSAELVASLQELRPRLVVACDLPSGLDANTGEVHWPVLEADVTVTFGGVKAGLMTDPGEGCAGRVHVVEIGIEGSLESQQPELRRLTSQDVGAVLPHPGRRAHKYSRGVLGVVAGSVRFAGAAVLGVHAAALAGAGMVRYAGPQTVGQLVLAQTPEALWEPDEPGRVQAWLLGSGVDGEEQLQRAKDAAAAALAADVPVVVDAGALSLLPDRCPPHWILTPHAGELATLLDSLPSTGEVAVTRDDVESRPLHFVRQAAEQTGATVLLKGATTLVASPSGVVFSQSEGTAWMATAGSGDVLGGVLGALLAQCAETIKDDDGAYAGLGLDVADRWAALAAVAASVHGRAGSAASAELAGGPITASAIMAAVPRVLGSLNAECDPSRP
>NZ_CP022436.1|WP_011775548.1|3618930_3619278_-|holo-ACP-synthase
MIVGIGVDVVDIERFGRQLERTPGLRDRLFVPAERELNTRSLAARFAAKEAVAKVLGAPAGMNWQDCWIGLDENGPTVQVKGTVLAVAEAKGVKRWHLSMSHDGGIATATVLAEG
>NZ_CP022436.1|WP_089595772.1|3619282_3621166_-|glutamine--fructose-6-phosphate-transaminase-(isomerizing)
MCGIVGYVGNSSRKAAGHSALDVVVEGLRRLEYRGYDSAGVAVVADGTISSRKKSGKLSNLISELEANPVPESLTGIGHTRWATHGGPTDRNAHPHLSDGGRLALIHNGIIENFAELKQELLAKGVTFESETDTEVAAALVGDIFRTQLNGDGGNLTEAMRLACQRLEGAFTLLAVHADQPDVVVAARRNSPLVVGLGEGENFLGSDVSGFIDYTRRAVELGQDQIVTITADSVEITDFFGAPAEGKEYHVDWDPASAEKGGFNSFMEKEIHDQPDAVAQTLLGRSDLDGKLTLDEVRIDPELLKQVDKIIVLACGTAAYAGLVAKYAIENWCRIPTEVELAHEFRYRDPIVDSNTLVVSISQSGETMDTLMAVRYAREQGAKTISICNTNGSTIPRESDAVLYTHAGPEIAVASTKAFLAQITAAYLLGLYLAQLRGNIFSGQIKDVLADLNKIPAKIQKILDNAGPLRELARSMKDEKSVLFLGRHVGYPVALEGALKLKEIAYIHAEGFAAGELKHGPIALIDDGQPVFVVVPSPRGRDSLHSKVVSNIQEVRARGARTLVIAEEGDESVKDYAEHVFYVPETPTLLMPLLTTVPLQIFAAELAGAKGYDVDQPRNLAKSVTVE
>NZ_CP022436.1|WP_089597531.1|3622343_3623147_+|M15-family-metallopeptidase
MAALSSCTPETAVPSPAAANAASGAAAPSAAPSSAATTDPATFAPETAAPSPSAMPSSAAPSSAVVPQHSLTDPTSPWVIVNKHRPLNPQDFVPTDLVQPNIRLAVSGEASLMNSTTAAAAEKLFAAAATEGVVMTLASGYRSYSTQVATYGGYVASTGQAAADRASARPGHSEHQTGWSFDIADGGGACSFQPCFAEQPAAVWAKANAHKFGFVVRYPWMFHDITGYFYESWHLRYIGVEAATDMVARGIVTLEEYFGLEAAPDYL
>NZ_CP022436.1|WP_089595773.1|3623214_3624579_-|phosphoglucosamine-mutase
MSRLFGTDGVRGLANGLLTAELAMQLAQAAAVVLGHDRTTNGKRPRAVVARDPRASGEFLAAAVEAGLSSSGIDVYDAGVLPTPAAAYLVADLDADFGVMLSASHNPAPDNGIKFFARGGQKLPDHVEDAIEAQLGKEPQRPVGADVGRIQRFSDAEDRYIVHLLGTLPKRLDGLKVVLDCAHGAASGCSPQVFKDAGADVVVIGAEPDGLNINEGVGSTHLGPLKEAVLKHGADLGVAHDGDADRCLAVDHEGNEVDGDQIMAILALALNEAGKLKDSVLVATVMSNLGLKIALKSAGITIRETGVGDRYVLEEMRNGGYNLGGEQSGHVIFSDYATTGDGVLTGLQLAAQVALTGRSLKELSTAMTKLPQLMINVKGVDKARAGTDEGVAAAVAAAELELGETGRVLLRPSGTEALVRVMVEAADMETAERICNSLAAVVKERLGASSEMAV

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Crispr_ID: NZ_CP022436_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022436_3

4168542-4168700

Orphan

Consensus_repeat	Method
TGGCCGTCGGCGTCGGCGTCGGGCTTGCGGACGTTGGAGTCGGGGTTGCAGTGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022436_3

>merge|NZ_CP022436|3|4168542-4168700|CRISPRCasFinder
TCGGCGTCGGCGTCGGCGTCGGGCTTGCGGACATGGCCGTCGGCGTCGGCGTCGGGCTTGCGGACGTTGGAGTCGGGGTTGCAGTGGGGGTTGCGGTGGTCACGCTCGGCGTCGGCGTCGGCGTCGGGCTTGCGGACGTGGCCGTCGGCGTCGGCGTCG

>NZ_CP022436|3|3|4168542-4168700|CRISPRCasFinder
TCGGCGTCGGCGTCGGCGTCGGGCTTGCGGACATGGCCGTCGGCGTCGGCGTCG	GGCTTGCGGACGTTGGAGTCGGGGTTGCAGTGGGGGTTGCGGTGGTCACGC
TCGGCGTCGGCGTCGGCGTCGGGCTTGCGGACGTGGCCGTCGGCGTCGGCGTCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022436.1\|WP_089596171.1\|4176674_4178273_+\|malate-synthase-A	unknown	unknown	gnl\|CDD\|236432
NZ_CP022436.1\|WP_089596174.1\|4180448_4180760_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022436.1\|WP_089596164.1\|4163278_4164862_-\|NCS2-family-permease	unknown	unknown	gnl\|CDD\|225161
NZ_CP022436.1\|WP_089596159.1\|4156634_4157273_+\|nucleotidyltransferase-family-protein	unknown	unknown	gnl\|CDD\|133025
NZ_CP022436.1\|WP_089596162.1\|4160669_4161608_-\|FAD-binding-molybdopterin-dehydrogenase	unknown	unknown	gnl\|CDD\|366378
NZ_CP022436.1\|WP_089597604.1\|4170971_4171880_+\|urate-oxidase	unknown	unknown	gnl\|CDD\|274554
NZ_CP022436.1\|WP_089596175.1\|4180845_4181160_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226323
NZ_CP022436.1\|WP_026546905.1\|4174278_4175034_-\|IclR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224332
NZ_CP022436.1\|WP_089596163.1\|4161598_4162948_-\|XdhC-family-protein	unknown	unknown	gnl\|CDD\|379212
NZ_CP022436.1\|WP_089596168.1\|4172054_4173563_+\|purine-permease	unknown	unknown	gnl\|CDD\|274468
NZ_CP022436.1\|WP_089596160.1\|4157314_4157782_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP022436.1\|WP_089596170.1\|4175255_4176656_+\|NAD-dependent-malic-enzyme	unknown	unknown	gnl\|CDD\|223358
NZ_CP022436.1\|WP_089596173.1\|4179551_4180364_+\|(S)-ureidoglycine-aminohydrolase	unknown	unknown	gnl\|CDD\|183011
NZ_CP022436.1\|WP_089596172.1\|4178274_4179537_+\|aldolase	unknown	unknown	gnl\|CDD\|225184
NZ_CP022436.1\|WP_089597600.1\|4153414_4156201_+\|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	unknown	unknown	gnl\|CDD\|236500
NZ_CP022436.1\|WP_089596165.1\|4164868_4165363_-\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|238612
NZ_CP022436.1\|WP_089596166.1\|4165786_4167130_+\|8-oxoguanine-deaminase	unknown	unknown	gnl\|CDD\|236184
NZ_CP022436.1\|WP_089596161.1\|4157839_4160680_-\|molybdopterin-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|376913
NZ_CP022436.1\|WP_089597602.1\|4167237_4168296_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022436.1\|WP_089596169.1\|4173740_4174208_+\|DUF2867-domain-containing-protein	unknown	unknown	gnl\|CDD\|378548

Protein	Function_ID	Function_description	E-value
NZ_CP022436.1\|WP_089596171.1\|4176674_4178273_+\|malate-synthase-A	gnl\|CDD\|236432	PRK09255, PRK09255, malate synthase; Validated.	0
NZ_CP022436.1\|WP_089596164.1\|4163278_4164862_-\|NCS2-family-permease	gnl\|CDD\|225161	COG2252, COG2252, Xanthine/uracil/vitamin C permease [Nucleotide transport and metabolism].	3.44863e-111
NZ_CP022436.1\|WP_089596159.1\|4156634_4157273_+\|nucleotidyltransferase-family-protein	gnl\|CDD\|133025	cd04182, GT_2_like_f, GT_2_like_f is a subfamily of the glycosyltransferase family 2 (GT-2) with unknown function. GT-2 includes diverse families of glycosyltransferases with a common GT-A type structural fold, which has two tightly associated beta/alpha/beta domains that tend to form a continuous central sheet of at least eight beta-strands. These are enzymes that catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. Glycosyltransferases have been classified into more than 90 distinct sequence based families.	7.73184e-45
NZ_CP022436.1\|WP_089596162.1\|4160669_4161608_-\|FAD-binding-molybdopterin-dehydrogenase	gnl\|CDD\|366378	pfam00941, FAD_binding_5, FAD binding domain in molybdopterin dehydrogenase.	5.28145e-16
NZ_CP022436.1\|WP_089597604.1\|4170971_4171880_+\|urate-oxidase	gnl\|CDD\|274554	TIGR03383, Structure_Of_Uricase, urate oxidase. Members of this protein family are urate oxidase, also called uricase. This protein contains two copies of the domain described by the uricase model pfam01014. In animals, this enzyme has been lost from primates and birds. [Central intermediary metabolism, Other].	9.36646e-166
NZ_CP022436.1\|WP_089596175.1\|4180845_4181160_-\|hypothetical-protein	gnl\|CDD\|226323	COG3801, COG3801, Uncharacterized protein conserved in bacteria [Function unknown].	2.47258e-10
NZ_CP022436.1\|WP_026546905.1\|4174278_4175034_-\|IclR-family-transcriptional-regulator	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	2.23342e-67
NZ_CP022436.1\|WP_089596163.1\|4161598_4162948_-\|XdhC-family-protein	gnl\|CDD\|379212	pfam13478, XdhC_C, XdhC Rossmann domain. This entry is the rossmann domain found in the Xanthine dehydrogenase accessory protein.	7.62415e-49
NZ_CP022436.1\|WP_089596168.1\|4172054_4173563_+\|purine-permease	gnl\|CDD\|274468	TIGR03173, pbuX, xanthine permease. All the seed members of this model are observed adjacent to genes for either xanthine phosphoribosyltransferase (for the conversion of xanthine to guanine, GenProp0696) or genes for the conversion of xanthine to urate and its concomitant catabolism (GenProp0640, GenProp0688, GenProp0686 and GenProp0687). A number of sequences scoring higher than trusted to this model are found in different genomic contexts, and the possibility exist that these transport related compounds in addition to or instead of xanthine itself. The outgroup to this family are sequences which are characterized as uracil permeases or are adjacent to established uracil phosphoribosyltransferases.	2.14229e-178
NZ_CP022436.1\|WP_089596160.1\|4157314_4157782_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|366181	pfam00583, Acetyltransf_1, Acetyltransferase (GNAT) family. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	3.34882e-15
NZ_CP022436.1\|WP_089596170.1\|4175255_4176656_+\|NAD-dependent-malic-enzyme	gnl\|CDD\|223358	COG0281, SfcA, Malic enzyme [Energy production and conversion].	2.37598e-172
NZ_CP022436.1\|WP_089596173.1\|4179551_4180364_+\|(S)-ureidoglycine-aminohydrolase	gnl\|CDD\|183011	PRK11171, PRK11171, (S)-ureidoglycine aminohydrolase.	1.46176e-164
NZ_CP022436.1\|WP_089596172.1\|4178274_4179537_+\|aldolase	gnl\|CDD\|225184	COG2301, CitE, Citrate lyase beta subunit [Carbohydrate transport and metabolism].	0.00842654
NZ_CP022436.1\|WP_089597600.1\|4153414_4156201_+\|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	gnl\|CDD\|236500	PRK09405, aceE, pyruvate dehydrogenase subunit E1; Reviewed.	0
NZ_CP022436.1\|WP_089596165.1\|4164868_4165363_-\|nucleoside-deaminase	gnl\|CDD\|238612	cd01285, nucleoside_deaminase, Nucleoside deaminases include adenosine, guanine and cytosine deaminases. These enzymes are Zn dependent and catalyze the deamination of nucleosides. The zinc ion in the active site plays a central role in the proposed catalytic mechanism, activating a water molecule to form a hydroxide ion that performs a nucleophilic attack on the substrate. The functional enzyme is a homodimer. Cytosine deaminase catalyzes the deamination of cytosine to uracil and ammonia and is a member of the pyrimidine salvage pathway. Cytosine deaminase is found in bacteria and fungi but is not present in mammals; for this reason, the enzyme is currently of interest for antimicrobial drug design and gene therapy applications against tumors. Some members of this family are tRNA-specific adenosine deaminases that generate inosine at the first position of their anticodon (position 34) of specific tRNAs; this modification is thought to enlarge the codon recognition capacity during protein synthesis. Other members of the family are guanine deaminases which deaminate guanine to xanthine as part of the utilization of guanine as a nitrogen source.	1.25016e-44
NZ_CP022436.1\|WP_089596166.1\|4165786_4167130_+\|8-oxoguanine-deaminase	gnl\|CDD\|236184	PRK08203, PRK08203, hydroxydechloroatrazine ethylaminohydrolase; Reviewed.	0
NZ_CP022436.1\|WP_089596161.1\|4157839_4160680_-\|molybdopterin-dependent-oxidoreductase	gnl\|CDD\|376913	pfam02738, Ald_Xan_dh_C2, Molybdopterin-binding domain of aldehyde dehydrogenase.	2.86345e-171
NZ_CP022436.1\|WP_089596169.1\|4173740_4174208_+\|DUF2867-domain-containing-protein	gnl\|CDD\|378548	pfam11066, DUF2867, Protein of unknown function (DUF2867). This bacterial family of proteins have no known function.	2.65271e-21

>NZ_CP022436.1|WP_089597602.1|4167237_4168296_-|hypothetical-protein
MSVYYGKPEHATQLKDIGVNVYQNAEHDGSTMASITNTGMLVIAGTEWSRTEVGSNPNVVGWDTYDECDMLGLGCNGSTYEQNLQQMKDKVAQIRGFNDGRFAFANYSKGILGTYWAPGLMDDFMAAVDAASVDNYMYARADLQDELNRTPAWPEGANTATSAAYGWQIDQMRKFQSAPGIHPNWIFVESARPFLNASNDRTITPEQMEGAMWSGIIHEARGISIFQHNNNGQAGFGTYSLVQAPADRKAKIKTALAGIQSLAPVLNTQSYVWDAGAAGTDTMLKAKDGSAYLFAGIGVNGGTGSKTFTLPAGITGTQVEVVGENRTISVQNGKFTDSFANEYTHHIYKITI
>NZ_CP022436.1|WP_089596166.1|4165786_4167130_+|8-oxoguanine-deaminase
MTRLWIKNPLGIFTANDLDAGGGLVVSDGKIVELVPSGGQPSTPAAVFDASSHVVLPGLINTHHHFYQTLTRAWGPVANAPLFPWLQNLYPVWARLTPRSLELAVQVALAELLLSGCTTAADHHYLFPDGMEDAIDIEVAAVRSMGMRATLTRGSMTLGEDDGGLPPRTTVQSPEAILADSERLIRQYHETGDGAVVQIALAPCSPFSVTKEIMAESAAMAERFDVRLHTHLAETIDEEDFCRSMFGLRTVDYLESVGWLGNRTWLGHGIHFNDEEIARLGAAGTAVAHCPTSNMRLASGTARVLELEAAGVPVGLGVDGSASNDASNMILEARQALYLQRLRYGASVPVERALGWATRGSAAVLGRSDLGQLAPGMQADLALFKPDSLRFSGSHDPVAALLLCGADRADRVMVGGVWRVVDGAIPGLDVAGLIAEHSAAARKLVAG
>NZ_CP022436.1|WP_089596165.1|4164868_4165363_-|nucleoside-deaminase
MSTTVTAEQFLATSIELATANVLNSGGPFGAVIVTADGRAFEGVNRVTATNDPTAHAEVTAIRNACRELGTFDLSGATLYTSCEPCPMCLASALWARVDRVFFAADRHDAASVGFDDAVFYEYFENDNRDALMPVAKLELGDPQAPAALQPFTTWNTLDSRIDY
>NZ_CP022436.1|WP_089596164.1|4163278_4164862_-|NCS2-family-permease
MADMTILDNSAEKQTAAEKQAALFPQGDSAEPTAAKHTATGLAGGNKKPPVSNSFLDKFFQISKRGSTLAREFRGGLVTFFTMAYIVILNPLILGGFSAENAPTDVAGGWLSAAQVGAVTGLTAGVMTIIFGLVANLPFGLAAGLGINSFLAVAVIQEVTWPEAMGLVVINGILIVIFGATGARTAIFKAVPKELKAAITVGIGLFIAFIGFVDSGFVRATTGGPPVQLGDNGSITSIPTLVFIIGLLTMGILVARKIQGGLLIGIVATTVLAAVAEAVFRIGPGSADNPGGWHLNVPILSSQLVSVPDLSLVGQFDLFGSFARIGGLAATMLVFTLVFTNFFDAMGTMTGLAKSAGVAHKDGTFPKLKSAFIVEGMGAVVGGATSGSSNTVYIDSAAGIGEGARTGLASVVTGLLFLGSMFFTPLTSVVPLEVAAAALVVVGAMMMAQIREIKFTKFSIALPAFLTIVTMPLTYSIANGIGVGFISFAVISAASGKAKKVHPLMWVVTAGFIIYFARGPINALMGV
>NZ_CP022436.1|WP_089596163.1|4161598_4162948_-|XdhC-family-protein
MLDLMPSLGSWRPAVSGQRCAVATIVGTGGSVPRPMGTSMMVSEQGEILGSLSGGCVEGAVVEAALEAMRDGGPRLESFGYSSEDAFAAGLTCGGELEVHIQPLGAGSPELSVFTELSAFTGLSSFQGQSTMAHPVEAHPAEAPPAVAPPAVALIRRLDAVGGVVVVHDPVRFRAMESEELAKLVGDHPSTLFAAAAQVEPLLQGGRAGLVRLAPPEGCIDGWVTTDRWAAEHQEEETQPEPITLFVESRLPAARMLIFGANDFGAALLPAGQLLGYNVTLCDARPAFARQSRFAGADQVVTDWPHRYLEAEAAARRIDNRTVVCVLTHDPKFDIPLLETALRFNLAYVGAMGSRRSHRQRVDALLEAGTPPESLERLHSPIGLNLGAVTPAEVAVSITAEIVAERGAAAAERGAGTTGFPSLKDSTGPIHPAPIHPAPQHLTQEDPWT
>NZ_CP022436.1|WP_089596162.1|4160669_4161608_-|FAD-binding-molybdopterin-dehydrogenase
MDMNTIEAVVPTTDPAQWRDGDAWLAGGTVLFSYGSTVLKRLLDLGQAEWPAITVTDAGIELAATCTVAELYALPQTAETASREWPGLALIRPCCDSFVASFKIWNMSTVGGNICTGLPAGPMTSLCAGLDGVATILGPDGGSRKVPVSDVVTGDMQTALEPGELLRSIHLPASALSARVAFRRLSLSNLGRSGVLLIGRLDPDGGLVITVTASTKRPVQLRFPAGQVPDAGTLADAVGDSIPWPLYHDDIHGLPAWRRDMTFKLAEEIRAELLGESMTVSGDFWPPHSTSPQPSTQPALSTTQQKEAPNGN
>NZ_CP022436.1|WP_089596161.1|4157839_4160680_-|molybdopterin-dependent-oxidoreductase
MAIEINGTASQATPRPGQCLRTFLREEGNFGVKKGCDGGDCGACTVHVDGAPVHSCIYPAVRAEGKSVTTIEGLSTAEGLHPVQEQFLEAQGFQCGFCTAGMMMTAATFDDEQRANLPRNLKGNLCRCTGYRSIADAVCGHGGDHQHDAGADVSGAQSVAGTQPGSGAQPAAVPATPGQLGDNVPAPAGPAIVTGTARYSLDVPAEQLPGLLHMKLLRSPHPHARIVSIDKAPALAVPGVVAVFTHEDAPQLLFSTAQHENYTDDPDDTRVLDNVVRFIGQRVAAVVAESVGAAEAGARALDVQYELLESVFTPQEAILPGAPAIHGEKDGVFSRISRPLQNVVAEVHAELGSVADGFAAADFIHEHTYQTQRVQHVAMETHASIAWLDEEGRLMIRSSTQVPFLVKRTLSRVFNLAPETIRVVAGRVGGGFGGKQEVLTEDLVALAALALRRPVQLEFTRTEQFTATTTRHPFTIHLKAGASRDGSLTALQLNVLTNTGAYGNHAPGVMFHGCGESLAVYKCVNKKVDAHAVYTNTVPAGAFRGYGLSQMIFAIESAIDELAVGIGMDPLEFRLKNMVRPGDHMLSTTPEPEEDVHYGSYGLDQCVALVRDALDRGKERYRAAGLDDLGPDWVVGEGSALSMIDTVPPRGHFAHTRVSLEANGRFAVDVGTAEFGNGTTTVHAQLAATALATTASKVAVRQSDTDLLEHDTGAFGSAGTVVAGKATLGAALELATRIQTVAASLTGAALTDCRLVDGAVECGDRTVTLTEIVDAARLQGVRLATDGNWGGTPRSVAFNVHGFRVAVNTGTGELRILQSVQAADAGVVVNPRQCRGQIEGGIAQALGAVLYEEVKVDDAGRVTTDILRQYHIPSFADVPRSEVYFATTNDSTGPLGAKSMSESPFNPVAPALANAIRNATGIRFGELPIARDKIYLALRDRTTAPV
>NZ_CP022436.1|WP_089596160.1|4157314_4157782_+|GNAT-family-N-acetyltransferase
MIRIDLDDPARPDVHQLLSEHLADMFATSPAESVHALDHSALSHESITFWTAREDGVLLGCGALKTLSAGQAEIKSMRTTATARGRGVATLMLEHIVADARGRGFERLSLETGTEDYFAPARRLYARHGFAECPPFGDYTLDPNSVFMELAVSPK
>NZ_CP022436.1|WP_089596159.1|4156634_4157273_+|nucleotidyltransferase-family-protein
MHPRAYREDMTDSGMAPTTGVLLAAGAGTRLGRGPKALLPFRGRTLVEVLANTLFDGGCREVVVVLGAEADRVRSVTDLGPYVVVENEQWGKGMAGSFRAGIDAATPGNSIMVALVDQPGLTPTAVSRLLGSHRPGRVTAAAYPDESGHLKRRHPVIFDVGLRAEAASAAHGDTGARSFLKAHPGLVDLVDCSDVCSGEDLDTKDQLHLLEL
>NZ_CP022436.1|WP_089597600.1|4153414_4156201_+|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type
MAAGEETSHILSGLTAQLPDRDPEETAEWIESLDALIAEQGTERAQYIMRSLLQRAGARSVGVPMVTTTDYVNTIPVDQEAEFPGNEEFERRYRAYMRWNAAVMVHRAQRADIGVGGHISTYAGAATLYEVGFNHFFRGKDHPSGGDQVFFQGHASPGMYARAFMEGRLTEEDLDGFRQEKSKAGHALSSYPHPRLMPDFWEFPTVSMGIGPMNAIYQAQSNRYLQNRGIKDTSDQQVWAFLGDGEMDEPESRGLLQLAANENLDNLNFVINCNLQRLDGPVRGNGKIMQELEAFFRGAGWNVIKVVWGREWDSLLEADQDGALVKIMNETPDGDYQTYKAESGGFVREHFFGKSPQTKDMVADLDDEQIWGLKRGGHDYRKVYAAYKAATEFKGKPTVILAKTVKGYGLGPHFEGRNATHQMKKLTMEDLKAFRDHLRIPISDDQLDADLYRPPYYHPGMDAPEIKYLMERRAELGGFVPERRRKHTDVTLPEAKSYDVAKRGSGKQQAATTMAFVRLLKDLMRDKNFGARFVPVVPDESRTFGMDAFFPTAKIYNPKGQNYLSVDRDLVLAYKESPAGQLIHPGINEAGAVAAFTAAGTAYATHGEPLVPIYVFYSMFGFQRTGDSFWAAADQMTRGFIIGATAGRTTLTGEGLQHADGHSPILASTNPAVKTYDPAYGYEIGHIIRHGLEEMYGPDADAQGTGTASDKNVMYYLTVYNEPITQPAEPENLDVNGLLKGIYHLAEAPTADGTNTANRPTAAILASGVSVPWALEAQRILAEDWNVAAEIYSVTSWNELRRDGLAAEEHAFLNPGQPARTPFITEQLAGHTGPVIAVTDYMKAVPDQIRQFIPNDFASLGADGFGFSDTRQAARRYFKNDTHSIVAKTLQLLAARGEVEEGAPSYAIDRYKLLDVNAGTTGGAGGDA
>NZ_CP022436.1|WP_089597604.1|4170971_4171880_+|urate-oxidase
MSNNIVLGENQYGKAEVRVVKVTRDTDRHHIEDLNVTSQLRGDFQAAHLEGDNGHVVATDTQKNTVYAFAREGIGSPESFLLRLADHFTGGFDWVSGGRWEAEAYSWDRIQAHGEGHDHSFVRNGQEVRTAVVVRDGATTHLISGLKDLTVLKTTQSGFVGYPRDKYTTLPETTDRILATDVSARWRYNTNLDFAGTDFNKSYEDIKALLLEGFTENYSHALQQTLFDMGKKVLEAHSEVDEIKFSMPNKHHFLVDLSPFGLDNPNEVFFAADRPYGLIEATVQRENIAAAPVAWSGIAGFC
>NZ_CP022436.1|WP_089596168.1|4172054_4173563_+|purine-permease
MNIKKKSRPANTTSSRKHQPERPEDKRLSIGSTFAYGFQHVLTMYGGIIAPPLIIGAAAGMSSQDIGLLIAACLFVGGLATILQTVGIPWFGSQLPLVQGVSFAGVSTMVAIVQGGGGIQAVFGSVIVASLIGLAITPLFSKIIKFFPPVVTGTVITTIGLTLMPVAANWAMGGNAKADNYGSMANIGLAAATMGVVLLLSKVGNAAISRLSILLAMVIGTIIAFVAGMADFSKVGQGDIVAFPTPFAFGAPTFEIAAIISMLIVILVTLTETSADIIAVGEIVDTKVDSRRIGDGLRADMLSSAISPLFNSFTQSAFAQNVGLVAITGIKSRFVVSAGGLILVILGLLPILGRVVAAVPTPVLGGAGVVLFGTVAASGIRTLAKVEYKNNMNLIIVAASIGFGMIPIAAPSFYDAFPSWFSTIFHSGISSAAVMAILLNILFNHFKAGNSDNQSVFVAGTDRIVSEEDIKCLSEGDRFENGKLIDADGKEVPLKTSSASEH
>NZ_CP022436.1|WP_089596169.1|4173740_4174208_+|DUF2867-domain-containing-protein
MTEQAPCFHSLAFREIPTPDYADVCLAVLPEGAGTDPTEWAERLFSLESMPRCVAAAMGLRQALVPLIGVPKAPQDTFKVSEQSGEEALIFVRDKHLDFAAAVGVDPVGRLIRVTTAVVLKGWRGKLYFSVVRPVHPIVVNSMLKKATRSQPTPS
>NZ_CP022436.1|WP_026546905.1|4174278_4175034_-|IclR-family-transcriptional-regulator
MAEKASGGVQSVERVFELLELITDAGGDVTLSELSSSTDLPLPTIHRLLRTLVSLGYIRQLPNRRYALGPRLIRLGEGASKQLGAVARPQLKTLVERLGETSNMAVLDSDMVIYVAQVPSMHSMRMFTEVGRRAHTHDTGVGKAILAQLDDEVVRGIVARTGMPTPTAKSIGDIDSLLADLALIRERGYSIDEEEQELGVRCFAMAVPNAPTPTAISVSGPITRVDQSFADRAVPMLREAAMAISAELNQN
>NZ_CP022436.1|WP_089596170.1|4175255_4176656_+|NAD-dependent-malic-enzyme
MANPSPGNSITLRVAAPSSFTATSELAAAVGAAGAAITALDVTESHHETIVVDVTCNTTDDDHAARVKDALNALDGVTVQHVSDRTFLMHLGGKLEVVPKVALRNRDDLSRAYTPGVARVCMAIAEDPAAARNLTVKRNTIAVLTDGSAVLGLGNIGPAAALPVMEGKAALFKQFANVDAWPVCLDTQDTEEIIMIAKAMAPVYGGINLEDIAAPRCFEIENRLREELDIPVFHDDQHGTAIVTLAALVNALRVVDKKLSEVKIVVSGVGAAGSAIIQLLKAQGAQHIIAAGRSGAIHSGEKYDDEHRSWIAANTNEEGFSGTLHDALKGADVFIGVSAPHVIGEEQVASMAEDAIVFAMANPTPEIDPVVASKHAAVVATGRSDFPNQINNVLAFPGFFRGLLDAGASDITPNMLVAAAEAIANRVADDELNASYIIPSVFDPHVAADVATAVANAAHANAASAL
>NZ_CP022436.1|WP_089596171.1|4176674_4178273_+|malate-synthase-A
MAITVTDPRPIDRAEEILTPKALAFIEELHKRFAGTRNELLEARGVKRQKVADTSRLDFLPETQDIRDGDWKVAEAPAALQDRRVEMTGPATPAKMAINALNSGAKVWLADLEDASTPTWPNVIDAILNLRDAAQGTLSFTSPEGKEYRLRTDAPLAVVVARPRGWHMEERHLLIDGEPAVGALVDFGLHFFHIAKQLLLNGHGPYYYLPKMESHLEARLWNDVFVFAQDFLGIPQGSVRATVLIETIPAAFEMDEILYELRDHASGLNAGRWDYLFSIIKYFRDAGEEFVLPDRATVAMTAPFMRAYTELLVKTCHKRGAFAMGGMAAVIPNRKQPDVTAAAFDKVRADKTREANDGFDGSWVAHPDLVSTCREVFDSVLGDRPNQLDKQRPEVSVTAEQLIDVASAGGTVTEAGLRLNLYVAVAYTGVWISGSGAVAIHNLMEDAATAEISRSQVWQQIRNKSVLADTGNTVTRELVSRILGEETERLRIEFGDENFKAYYEPASKLIEDICLSDDYTDFLTTPAYELVG
>NZ_CP022436.1|WP_089596172.1|4178274_4179537_+|aldolase
MGSFSSSDLAHIESQLAATDQLLDRNYPGDDGSRQPIHTVYIPADRFTPSLAAEWGAQALATAEAHGGLEKLGQLLGQESHLAAAVAERVAAKLSAEPIEDLRLDFEDGYGDRGDEAEDADAVAAAKAVATAVAAGTAPPFIGIRFKCFEAPTRARGLKTLDLFVSTLAEAGELPAGLILTLPKVTTVAQVQAMDYAVTRLEEVHGLPAGRLRFEVQVETPQLIIGADGTSPVAQLPHVVPGRISSLHYGTYDYSASLGISAEYQSMEHPVADFAKEVMQLAVAGTGIRLSDGSTNIIPVGDGVEDAWKLHGRLVRRSLENGYYQGWDLHAAQLPSRFSASYAFYREGLPAAALRLRNYVERTEGGVMDEPATARALAGFVLRGVQCGAVATDEVKALAGVELSQLTALAHPRLAQPTSH
>NZ_CP022436.1|WP_089596173.1|4179551_4180364_+|(S)-ureidoglycine-aminohydrolase
MGKYYYPQGGLPPQTQLTTERAIVTEAYTVIPKGVMTDIVTSNLPGFSNTRSWIIARPISGFATTFSQLIVEIAPGGGAPKAEFESGVEGVIFVTKGQVNLTLDGELHHLEEGGYAYLAAGSEWGLENVSDDIVSFHWIRKAYERLEGFEAKSFVTNEKDVEPTSMPDTDDVWKTTRFTDSSDLAHDMQVNIVTFQPGGVIPFPETHVMEHGLYVLEGKAMYLLNNDWVEVEAGDFMWLRAFCPQACYAGGPGEFRYLLYKDMNRQVKLT
>NZ_CP022436.1|WP_089596174.1|4180448_4180760_-|hypothetical-protein
MGERNISGEQNTPQPARRLAAVVVPLLGLIAVIAGVVVAWSNLETNVGWFAYAPLSNEVFVGDNGSFVSKGTQLGLAVAGVGLLVLAFWAGLAIGRRGSHPER
>NZ_CP022436.1|WP_089596175.1|4180845_4181160_-|hypothetical-protein
MATEDDIRRICLGMPGVSERPSWGQPAWFAKTLMARIWEEGVGTVKTDEREALAAMEPDTFFWTPHHDQSPQLMLIRLERIGTDELDELLQESYRIAGGPGKPN

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Click the colored protein region to show detailed information

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP022436_2	2.1\|3608218\|56\|NZ_CP022436\|CRISPRCasFinder	3608218-3608273	56	NZ_CP022436.1	3608283-3608338	0	1.0

1. spacer 2.1|3608218|56|NZ_CP022436|CRISPRCasFinder matches to position: 3608283-3608338, mismatch: 0, identity: 1.0

gctctctcacatcccgcgcccttccagacccaccgtctctcacatcccgcgccctt	CRISPR spacer
gctctctcacatcccgcgcccttccagacccaccgtctctcacatcccgcgccctt	Protospacer
********************************************************

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

1108313 : 1115953

Human_herpesvirus(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_089593892.1\|1108313_1109084_-	uracil-DNA glycosylase	A0A0N9SDW0	Human_herpesvirus	3.6e-24	38.5
WP_089593893.1\|1109190_1109526_+	DUF3263 domain-containing protein	A0A0A7RXU7	Mycobacterium_phage	2.6e-11	53.0
WP_089593894.1\|1109575_1110184_+	LytR C-terminal domain-containing protein	NA	NA	NA	NA
WP_011773737.1\|1110355_1110559_+	cold-shock protein	Q9AZD3	Lactococcus_phage	1.2e-16	62.7
WP_089593895.1\|1110882_1112508_+	chaperonin GroEL	A0A240F779	uncultured_virus	3.4e-149	54.5
WP_089593896.1\|1112718_1113858_+	ribonuclease HI family protein	A0A142CJN1	Brazilian_marseillevirus	7.5e-18	35.9
WP_089593897.1\|1113998_1114289_-	WXG100 family type VII secretion target	NA	NA	NA	NA
WP_089593898.1\|1114486_1115953_-	HAMP domain-containing histidine kinase	W8CYF6	Bacillus_phage	9.0e-24	30.6

DBSCAN-SWA_2

3082246 : 3105526

Arthrobacter_phage(35.29%)

terminase,portal

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_089595361.1\|3082246_3082738_+	single-stranded DNA-binding protein	A0A249XNK4	Arthrobacter_phage	1.3e-59	95.9
WP_157731816.1\|3083002_3083197_+	hypothetical protein	NA	NA	NA	NA
WP_089595364.1\|3084120_3084417_+	hypothetical protein	NA	NA	NA	NA
WP_157731818.1\|3084413_3084710_+	hypothetical protein	NA	NA	NA	NA
WP_089595366.1\|3084699_3085563_+	hypothetical protein	A0A1B3AZY7	Gordonia_phage	3.4e-31	40.7
WP_089595367.1\|3085559_3086699_+	AAA family ATPase	V5R9D2	Arthrobacter_phage	3.3e-130	66.6
WP_157731820.1\|3086692_3086863_+	hypothetical protein	V5R9D2	Arthrobacter_phage	4.1e-13	74.5
WP_157731822.1\|3086859_3087045_+	hypothetical protein	NA	NA	NA	NA
WP_089595369.1\|3087037_3087502_+	hypothetical protein	V5R8T9	Arthrobacter_phage	7.7e-46	61.9
WP_157731824.1\|3087606_3087939_+	hypothetical protein	NA	NA	NA	NA
WP_089595371.1\|3087935_3088220_+	hypothetical protein	NA	NA	NA	NA
WP_089595372.1\|3088216_3088474_+	hypothetical protein	NA	NA	NA	NA
WP_089595373.1\|3088470_3088902_+	ASCH domain-containing protein	A0A160DEV7	Gordonia_phage	4.4e-19	41.1
WP_089595374.1\|3088898_3089237_+	hypothetical protein	NA	NA	NA	NA
WP_089595375.1\|3089352_3089748_+	hypothetical protein	A0A0A7HAR9	Arthrobacter_phage	1.7e-22	52.5
WP_089595376.1\|3089750_3089981_+	hypothetical protein	NA	NA	NA	NA
WP_157731826.1\|3090058_3090478_+	HNH endonuclease	A0A088FQF5	Mycobacterium_phage	4.8e-23	45.3
WP_089595378.1\|3090474_3090702_+	hypothetical protein	NA	NA	NA	NA
WP_157731828.1\|3090730_3091003_+	hypothetical protein	NA	NA	NA	NA
WP_089595380.1\|3091523_3091994_+	hypothetical protein	NA	NA	NA	NA
WP_089595381.1\|3092071_3092323_+	hypothetical protein	NA	NA	NA	NA
WP_089595382.1\|3092973_3093459_+	hypothetical protein	A0A1J0MCI5	Streptomyces_phage	7.6e-12	33.1
WP_089597461.1\|3093505_3094753_+\|terminase	PBSX family phage terminase large subunit	A0A1J0MC90	Streptomyces_phage	1.8e-113	49.2
WP_089595383.1\|3094859_3095114_+	hypothetical protein	NA	NA	NA	NA
WP_157731830.1\|3095123_3096698_+\|portal	phage portal protein	A0A162E1F1	Gordonia_phage	7.8e-82	39.6
WP_157731832.1\|3096654_3097806_+	hypothetical protein	A0A1J0MCS2	Streptomyces_phage	3.4e-34	33.3
WP_089595386.1\|3097832_3098552_+	hypothetical protein	NA	NA	NA	NA
WP_089595387.1\|3098567_3099521_+	hypothetical protein	A0A2H5BLW0	Streptomyces_phage	2.4e-102	62.3
WP_089595388.1\|3099541_3099853_+	hypothetical protein	A0A1C9EHZ8	Gordonia_phage	1.8e-22	66.7
WP_089595389.1\|3099868_3100294_+	hypothetical protein	A0A1J0MC70	Streptomyces_phage	5.3e-09	36.1
WP_157731834.1\|3100286_3100604_+	hypothetical protein	NA	NA	NA	NA
WP_089595391.1\|3100612_3100945_+	hypothetical protein	NA	NA	NA	NA
WP_089595392.1\|3100952_3101414_+	hypothetical protein	NA	NA	NA	NA
WP_089595393.1\|3101464_3102166_+	hypothetical protein	A0A0U4JQQ8	Arthrobacter_phage	1.5e-13	58.1
WP_089595394.1\|3102254_3102695_+	hypothetical protein	NA	NA	NA	NA
WP_089595395.1\|3102874_3105526_+	hypothetical protein	A0A0K1Y5T7	Streptomyces_phage	3.6e-07	49.2

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_CP022436

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

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection