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_CP018174	Corynebacterium glutamicum strain XV plasmid unnamed, complete sequence	0 crisprs	NA	0	0	0	0
NZ_CP018175	Corynebacterium glutamicum strain XV chromosome, complete genome	3 crisprs	csa3,WYL,cas3,cas9,DEDDh,PrimPol,DinG,RT	0	0	4	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP018175_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP018175_1

360563-360658

Orphan

Consensus_repeat	Method
TGCGTGGGCAGTGTGGTTTGGTTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP018175_1

>merge|NZ_CP018175|1|360563-360658|CRISPRCasFinder
TGCGTGGGCAGTGTGGTTTGGTTTTGGGGGCTCGGAACCGGTCACAGATGCCCACGATTGCGGTTTTTCCGTTGCGTGGGCAGTGTGGTTTGGTCT

>NZ_CP018175|1|1|360563-360658|CRISPRCasFinder
TGCGTGGGCAGTGTGGTTTGGTTT	TGGGGGCTCGGAACCGGTCACAGATGCCCACGATTGCGGTTTTTCCGT
TGCGTGGGCAGTGTGGTTTGGTCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018175.1\|WP_065366576.1\|365183_366317_+\|TadA-family-conjugal-transfer-associated-ATPase	unknown	unknown	gnl\|CDD\|200328
NZ_CP018175.1\|WP_060563668.1\|352315_353260_+\|amidohydrolase	unknown	unknown	gnl\|CDD\|225070
NZ_CP018175.1\|WP_003863293.1\|362804_363647_-\|HAD-family-hydrolase	unknown	unknown	gnl\|CDD\|319796
NZ_CP018175.1\|WP_060563686.1\|367074_367650_+\|type-II-secretion-system-F-family-protein	unknown	unknown	gnl\|CDD\|224975
NZ_CP018175.1\|WP_003863295.1\|361078_362074_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP018175.1\|WP_060563671.1\|353252_354449_+\|glutaryl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|173840
NZ_CP018175.1\|WP_065532532.1\|364125_365187_+\|septum-site-determining-protein	unknown	unknown	gnl\|CDD\|274798
NZ_CP018175.1\|WP_060563678.1\|362088_362640_-\|phage-holin-family-protein	unknown	unknown	gnl\|CDD\|377816
NZ_CP018175.1\|WP_060563688.1\|368220_368520_+\|flp-pilus-assembly-TadE/G-like-family-protein	unknown	unknown	gnl\|CDD\|274799
NZ_CP018175.1\|WP_060563677.1\|359314_360511_+\|MarP-family-serine-protease	unknown	unknown	gnl\|CDD\|367140
NZ_CP018175.1\|WP_060563685.1\|366301_367078_+\|type-II-secretion-system-F-family-protein	unknown	unknown	gnl\|CDD\|227300
NZ_CP018175.1\|WP_075348062.1\|357137_357920_+\|endonuclease-III	unknown	unknown	gnl\|CDD\|223255
NZ_CP018175.1\|WP_060563687.1\|367877_368198_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_040966841.1\|355961_356645_-\|Crp/Fnr-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223736
NZ_CP018175.1\|WP_003863309.1\|354470_354944_+\|MaoC-family-dehydratase	unknown	unknown	gnl\|CDD\|239534
NZ_CP018175.1\|WP_060563675.1\|357927_358488_+\|TlpA-family-protein-disulfide-reductase	unknown	unknown	gnl\|CDD\|239264
NZ_CP018175.1\|WP_060563676.1\|358480_359224_+\|CoA-pyrophosphatase	unknown	unknown	gnl\|CDD\|239518
NZ_CP018175.1\|WP_003863306.1\|356906_357092_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_075348061.1\|355040_355886_+\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293836
NZ_CP018175.1\|WP_003855827.1\|367673_367874_+\|DUF4244-domain-containing-protein	unknown	unknown	gnl\|CDD\|379429

Protein	Function_ID	Function_description	E-value
NZ_CP018175.1\|WP_065366576.1\|365183_366317_+\|TadA-family-conjugal-transfer-associated-ATPase	gnl\|CDD\|200328	TIGR03819, heli_sec_ATPase, helicase/secretion neighborhood ATPase. Members of this protein family comprise a distinct clade of putative ATPase associated with an integral membrane complex likely to act in pilus formation, secretion, or conjugal transfer. The association of most members with a nearby gene for a DEAH-box helicase suggests a role in conjugal transfer.	5.58238e-154
NZ_CP018175.1\|WP_060563668.1\|352315_353260_+\|amidohydrolase	gnl\|CDD\|225070	COG2159, COG2159, Predicted metal-dependent hydrolase of the TIM-barrel fold [General function prediction only].	5.19928e-87
NZ_CP018175.1\|WP_003863293.1\|362804_363647_-\|HAD-family-hydrolase	gnl\|CDD\|319796	cd02612, HAD_PGPPase, phosphatidylglycerol-phosphate phosphatase, similar to Escherichia coli K-12 phosphatidylglycerol-phosphate phosphatase C. This family includes Escherichia coli K-12 phosphatidylglycerol-phosphate phosphatase C, PgpC (previously named yfhB) which catalyzes the dephosphorylation of phosphatidylglycerol-phosphate (PGP) to phosphatidylglycerol (PG). This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	3.05942e-74
NZ_CP018175.1\|WP_060563686.1\|367074_367650_+\|type-II-secretion-system-F-family-protein	gnl\|CDD\|224975	COG2064, TadC, Flp pilus assembly protein TadC [Cell motility and secretion / Intracellular trafficking and secretion].	1.60236e-14
NZ_CP018175.1\|WP_003863295.1\|361078_362074_-\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	8.10411e-22
NZ_CP018175.1\|WP_060563671.1\|353252_354449_+\|glutaryl-CoA-dehydrogenase	gnl\|CDD\|173840	cd01151, GCD, Glutaryl-CoA dehydrogenase. Glutaryl-CoA dehydrogenase (GCD). GCD is an acyl-CoA dehydrogenase, which catalyzes the oxidative decarboxylation of glutaryl-CoA to crotonyl-CoA and carbon dioxide in the catabolism of lysine, hydroxylysine, and tryptophan. It uses electron transfer flavoprotein (ETF) as an electron acceptor. GCD is a homotetramer. GCD deficiency leads to a severe neurological disorder in humans.	2.05892e-107
NZ_CP018175.1\|WP_065532532.1\|364125_365187_+\|septum-site-determining-protein	gnl\|CDD\|274798	TIGR03815, CpaE_hom_Actino, helicase/secretion neighborhood CpaE-like protein. Members of this protein family belong to the MinD/ParA family of P-loop NTPases, and in particular show homology to the CpaE family of pilus assembly proteins (see ). Nearly all members are found, not only in a gene context consistent with pilus biogenesis or a pilus-like secretion apparatus, but also near a DEAD/DEAH-box helicase, suggesting an involvement in DNA transfer activity. The model describes a clade restricted to the Actinobacteria.	4.52424e-91
NZ_CP018175.1\|WP_060563678.1\|362088_362640_-\|phage-holin-family-protein	gnl\|CDD\|377816	pfam07332, Phage_holin_3_6, Putative Actinobacterial Holin-X, holin superfamily III. Phage_holin_3_6 is a family of small hydrophobic proteins with two or three transmembrane domains of the Hol-X family. Holin proteins are produced by double-stranded DNA bacteriophages that use an endolysin-holin strategy to achieve lysis of their hosts. The endolysins are peptidoglycan-degrading enzymes that are usually accumulated in the cytosol until access to the cell wall substrate is provided by the holin membrane lesion.	9.48535e-32
NZ_CP018175.1\|WP_060563688.1\|368220_368520_+\|flp-pilus-assembly-TadE/G-like-family-protein	gnl\|CDD\|274799	TIGR03816, tadE_like_DECH, helicase/secretion neighborhood TadE-like protein. Members of this small, highly hydrophobic protein family occur in a pilus/secretion-like region that usually is next to an uncharacterized DEAH-box helicase, in Actinobacteria. Members show sequence similarity to the TadE-like family described by pfam07811. The function is unknown. [Unknown function, General].	2.11014e-07
NZ_CP018175.1\|WP_060563677.1\|359314_360511_+\|MarP-family-serine-protease	gnl\|CDD\|367140	pfam02674, Colicin_V, Colicin V production protein. Colicin V production protein is required in E. Coli for colicin V production from plasmid pColV-K30. This protein is coded for in the purF operon.	2.02474e-18
NZ_CP018175.1\|WP_060563685.1\|366301_367078_+\|type-II-secretion-system-F-family-protein	gnl\|CDD\|227300	COG4965, TadB, Flp pilus assembly protein TadB [Intracellular trafficking and secretion].	2.72284e-66
NZ_CP018175.1\|WP_075348062.1\|357137_357920_+\|endonuclease-III	gnl\|CDD\|223255	COG0177, Nth, Predicted EndoIII-related endonuclease [DNA replication, recombination, and repair].	9.85454e-107
NZ_CP018175.1\|WP_040966841.1\|355961_356645_-\|Crp/Fnr-family-transcriptional-regulator	gnl\|CDD\|223736	COG0664, Crp, cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases [Signal transduction mechanisms].	8.3036e-56
NZ_CP018175.1\|WP_003863309.1\|354470_354944_+\|MaoC-family-dehydratase	gnl\|CDD\|239534	cd03450, NodN, NodN (nodulation factor N) contains a single hot dog fold similar to those of the peroxisomal Hydratase-Dehydrogenase-Epimerase (HDE) protein, and the fatty acid synthase beta subunit. Rhizobium and related species form nodules on the roots of their legume hosts, a symbiotic process that requires production of Nod factors, which are signal molecules involved in root hair deformation and meristematic cell division. The nodulation gene products, including NodN, are involved in producing the Nod factors, however the role played by NodN is unclear.	1.47997e-80
NZ_CP018175.1\|WP_060563675.1\|357927_358488_+\|TlpA-family-protein-disulfide-reductase	gnl\|CDD\|239264	cd02966, TlpA_like_family, TlpA-like family; composed of TlpA, ResA, DsbE and similar proteins. TlpA, ResA and DsbE are bacterial protein disulfide reductases with important roles in cytochrome maturation. They are membrane-anchored proteins with a soluble TRX domain containing a CXXC motif located in the periplasm. The TRX domains of this family contain an insert, approximately 25 residues in length, which correspond to an extra alpha helix and a beta strand when compared with TRX. TlpA catalyzes an essential reaction in the biogenesis of cytochrome aa3, while ResA and DsbE are essential proteins in cytochrome c maturation. Also included in this family are proteins containing a TlpA-like TRX domain with domain architectures similar to E. coli DipZ protein, and the N-terminal TRX domain of PilB protein from Neisseria which acts as a disulfide reductase that can recylce methionine sulfoxide reductases.	4.38626e-22
NZ_CP018175.1\|WP_060563676.1\|358480_359224_+\|CoA-pyrophosphatase	gnl\|CDD\|239518	cd03426, CoAse, Coenzyme A pyrophosphatase (CoAse), a member of the Nudix hydrolase superfamily, functions to catalyze the elimination of oxidized inactive CoA, which can inhibit CoA-utilizing enzymes. The need of CoAses mainly arises under conditions of oxidative stress. CoAse has a conserved Nudix fold and requires a single divalent cation for catalysis. In addition to a signature Nudix motif G[X5]E[X7]REUXEEXGU, where U is Ile, Leu, or Val, CoAse contains an additional motif upstream called the NuCoA motif (LLTXT(SA)X3RX3GX3FPGG) which is postulated to be involved in CoA recognition. CoA plays a central role in lipid metabolism. It is involved in the initial steps of fatty acid sythesis in the cytosol, in the oxidation of fatty acids and the citric acid cycle in the mitochondria, and in the oxidation of long-chain fatty acids in peroxisomes. CoA has the important role of activating fatty acids for further modification into key biological signalling molecules.	4.08015e-53
NZ_CP018175.1\|WP_075348061.1\|355040_355886_+\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293836	cd16278, metallo-hydrolase-like_MBL-fold, uncharacterized subgroup of the MBL-fold_metallo-hydrolase superfamily; MBL-fold metallo hydrolase domain. Members of the MBL-fold metallohydrolase superfamily are mainly hydrolytic enzymes which carry out a variety of biological functions. The class B metal beta-lactamases (MBLs) for which this fold was named perform only a small fraction of the activities included in this superfamily.Activities carried out by superfamily members include class B beta-lactamases, hydroxyacylglutathione hydrolases, AHL (acyl homoserine lactone) lactonases, persulfide dioxygenases, flavodiiron proteins, cleavage and polyadenylation specificity factors such as the Int9 and Int11 subunits of Integrator, Sdsa1-like and AtsA-like arylsulfatases, 5'-exonucleases human SNM1A and yeast Pso2p, ribonuclease J and ribonuclease Z, cyclic nucleotide phosphodiesterases, insecticide hydrolases, and proteins required for natural transformation competence. Classical members of the superfamily are di-, or less commonly mono-, zinc-ion-dependent hydrolases, however the diversity of biological roles is reflected in variations in the active site metallo-chemistry.	1.25158e-64
NZ_CP018175.1\|WP_003855827.1\|367673_367874_+\|DUF4244-domain-containing-protein	gnl\|CDD\|379429	pfam14029, DUF4244, Protein of unknown function (DUF4244). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 66 and 95 amino acids in length. There is a conserved EYA sequence motif.	1.21917e-15

>NZ_CP018175.1|WP_060563677.1|359314_360511_+|MarP-family-serine-protease
MLSPSLVVDAVIVLVMAFALWGGWRQGAFTSLLSTVGVVSGLVVGAAAAPFVMGLTDSTALRFLLAIGTVVLLVGLGNLIGAHLGAAIRDNIKFRSSRTLDSGLGAIFQVLATLIVVWLVAIPLATGLPGTVASGIRDSRILGFVDKYTPQGLDTLPSKIAAMLSESGLPPLISPFAGGSSVEVDAPEINVTNVDLVEAMRPSVIHVMGDAQECSRRLMGSGFVASPDYVVTNAHVVAGTSTVSLDTMIGTRSAEVVFYDPNLDIAVLYSPDLGLDPLPWASTPLDTGDEAIVMGFPQSGPFNASPARVRERIMITGSNIYANGQHEREAYSVRGSIQSGNSGGPMTNEMGEVVGVVFGAAIDGSDTGYVLTAEEVQERIGDITALTQPVDTMQCAVS
>NZ_CP018175.1|WP_060563676.1|358480_359224_+|CoA-pyrophosphatase
MRNYPDLPHDFPGQNTELTPAKAPVWMHRLLDRIHTGRMANPLDGAETLGDTDSEKRAAVLMLFSGSETSFDLPNDASVLLTHRTPTMRSHAGQIAFPGGRIDPTDTNAVDCAFREAWEETGLDRRTATPLAQLNEVHIRATGYPVYPIIGHWHTPSPVAVASPHETDEVFDAPLYDLIDPKNRLMVGWREWHGPAFRINDYIIWGFTGGLLSAILDTAGWATEWDTDRIFDLENTLSTSRNNERMR
>NZ_CP018175.1|WP_060563675.1|357927_358488_+|TlpA-family-protein-disulfide-reductase
MTSSAKWSIVGVVAILAVIVALIPQLVGGESAEEAQGETSTSKITTRPDCVASGAAGVDLPCLGGANGAGNELATVVNLWAWWCEPCRAELPIFDEFATTHPELNVIGVHADQNAANGAALLEDLGVNLASYQDDSNLFAGTLGLPGVVPITIVVSPDGNVVDTFPQPFETIDDLETAVAGALQNA
>NZ_CP018175.1|WP_075348062.1|357137_357920_+|endonuclease-III
MGSITPQKRPRVGSHIANKDQETDIGRKRRARRINRTLTVAYPDAHCELDFTNPLELTVATILSAQCTDVRVNQVTPALFKRYPTAADYANADRTELEEFIRPTGFYRNKAASLIGLGEALISLHDGQVPGTLEQLVELPGVGRKTANVVLGNAFGVPGITVDTHFGRLVRRLKLTDEEDPVKVEKVMNELIEKPEWTMFSHRLIFHGRRICHSRRAACGACMLAADCPSFGLEGPSDPFEAQKLIKSDDREHLLKMAGM
>NZ_CP018175.1|WP_003863306.1|356906_357092_-|hypothetical-protein
MTGLLVVIIPLLLMLFAFAMERIESSFLHSNAPQNTEVKLAKDAVGAENLNEDDVQEASAA
>NZ_CP018175.1|WP_040966841.1|355961_356645_-|Crp/Fnr-family-transcriptional-regulator
MEGVQDILSRAGIFQGVDPTAVNNLIQDMETVRFPRGATIFDEGEPGDRLYIITSGKVKLARHAPDGRENLLTIMGPSDMFGELSIFDPGPRTSSAVCVTEVHAATMNSDMLRNWVADHPAIAEQLLRVLARRLRRTNASLADLIFTDVPGRVAKTLLQLANRFGTQEAGALRVNHDLTQEEIAQLVGASRETVNKALATFAHRGWIRLEGKSVLIVDTEHLARRAR
>NZ_CP018175.1|WP_075348061.1|355040_355886_+|MBL-fold-metallo-hydrolase
MTKLERMEHPAYSQLRPVTPSASVVLCPNPGYSSLEGTNSWVIRAPEDPRSIVIDPGPEDEGHLNVLHSKAEEVGLILLTHRHHDHADGAQRFRQLTNAPVRAMDPSYCAGAEEIHDGEIITIDGVTPQIEVVATPGHTRDSVSYFIWSGVPHESTLEGIVSGDTIAGRHTTMISETDGDLGEYLNSLAILEERGKDIPLLPGHGPDGQDVASFARKYIERRELRLNQIREVWETRGRDVSMKDLIDAIYDDVDSVLRGAAEQSTHVAIRYLQAQEASASN
>NZ_CP018175.1|WP_003863309.1|354470_354944_+|MaoC-family-dehydratase
MTTSTTPNTIVSFEDAPTLTGQDLGFSQWRTVTQEMVNTFADATDDQQWIHTDPERAKDGPFGGAIAHGFLTLSMIIPFWGELLDVTGVTTKVNYGLDKVRFTSPVKVGSRIRMGAVVREISEVKGNGLHLVADGTIEIEGQERPAVVATFLTRFYA
>NZ_CP018175.1|WP_060563671.1|353252_354449_+|glutaryl-CoA-dehydrogenase
MRDPIQGAVIPSDLFGFAEVLTEAERAVLLETRRVLEEEVKPYINEAWDKAVFPNAIMQPLQDLQLLDPPALREAGESVRDIFTGFRNFELARCDINVGTYYNASAGLFRTACMVGGSAEQAQRLDAQIKSGEVKGVFALTEPDHGSDIAGGLATTATKDADTGEWIINGEKRWIGGASTADLIATFARDTADNQVKCFLVAPKAEGVSMEIIDRKASLRIMQNAHITYNNVRVSEDARLHNINSFKDVSECLRRMRSDVAWMAVGAQAGAYEAAVKYVRSREQFGRPIAGFQLIQEKLALMLGNLTASLGMMVKLTEQQQAGIFKEENSALAKMFTSLKLRETVGWAREICGGNGIILDNDVARFHADAEAVYSYEGTHEINALIVGRAITGVSAFI
>NZ_CP018175.1|WP_060563668.1|352315_353260_+|amidohydrolase
MSNNVVKYECAVDADNIVAVDMHVHLEVDSCGHESMPADIMEASSKYFKAAERTPSADAIADIYREHKMAAVVFTIDARTQMGHLPNSIDDLVASCARNNDVLIPFGSVDPRTGEDALVEARRQVEELGVRGFKFHPSVQGFDPSAPEFYPLWELLESFGLPCVFHTGQNGMGAGLPGGRGIKLRFSNPLLLDDVAADFPNLTIIMAHPSVPWQDEANSIATHKANVFIDLSGWSPKYFPESLVRQSNNVLSKKVLFGTDFPLITPEKWLAAFANLPLKDEVRPGILKDNAVKVLGLAASTERGSQAEKAVQHA
>NZ_CP018175.1|WP_003863295.1|361078_362074_-|alpha/beta-hydrolase
MAFFSFSTSPLTRLIPGSRSKATGAKRRLSSTIASIERSPGIIALDGPFTHDHVSVRGIRLHLAEAGSPTNPLVLLIHGAFGGWYDYREVIGPLADAGFHVAAIDLRGYGMSDKPPTGYDLRHAAGELSSVIAALGHDDALLVGSDTGASIAWAIASMYPERVRGLISLGAIHPLDMRRAIRRKPHLHVSDLSRLAPFRLPSFLHNLFHFGITSEARREIVNNTSSSYQRSNAFTETVLLRKKALSIDHTITPIIRTNRYLVGSIPSKTVSAPVWLLRTNTRRWEHLANTARTRTTGPFTTIAIPGGYELPYLENPSEFAATIAEFARTTF
>NZ_CP018175.1|WP_060563678.1|362088_362640_-|phage-holin-family-protein
MSNKDGLFTDGSSTFAPKVDSIPLSDVDTSVSGEASIGTLISNATSQMSSLFRAEVELAKTELAGEAKKAAIGGGAFSVAGVIALYSSFFFFFFVAALLSEWIKPWAAFLIVFLFMLVIAAALALFGWRKVKKMGAPKNTIQSVNQLKNLVPGQASEKLEKANKRGLYTSASFHSPGAITGNH
>NZ_CP018175.1|WP_003863293.1|362804_363647_-|HAD-family-hydrolase
MKHPDPAQKVEGTTATTPTKVAAFFDLDKTIIAMSSTYAYGREFMNSGLISPVEALQLSLAQATYMFAGHTSEQMDNTRDQLTAMIRGWEVQQVRSIAEETMHSVVTPTIYAEARELIEHHQELGHDVIIISASVKELVEPIARELGVHKTVTTVLEAHDGMYTGEVLFYCKGDAKAQSILDLAEANNYDLSLSFAYSDSFTDLPMLEAVGNPAAVNPDRALKKIALEQGWKILSFKNPEPLFQMPSTRDVGIGTGVVAGIAAVAAGSIWWMKRARRGSA
>NZ_CP018175.1|WP_065532532.1|364125_365187_+|septum-site-determining-protein
MNTITHQAILIAVEDPVLHPEAMHVAAATGRPVIETTNLMDISRHFHRASAVLIDASMASQLSPGKRRDRVFLLDSDPGPSDWKTAMKIHAEQAMLLPAQAGELLSALGRDDKQLPVASGHVIGVAGVVGGTGASTFAAALAKRRAESATTVLIDADPSSGGIDLLLGIEDVPGARWPDVGLRRGTVQAADVLKALPSTPDEVVVLSTARSNVLDPFALSESDVSAAIDCFLSADRSVDVVVDLPHARVHPDIAERLSHLVLVIPAEVRAVAAARARYMELQQLHVSITCVLRHRGWSGLDVAEVEEILGADITAEIGSIQRLAKSVEMHGLTGSLPRVLSSACDAVLGEVAA
>NZ_CP018175.1|WP_065366576.1|365183_366317_+|TadA-family-conjugal-transfer-associated-ATPase
MTDIDLVVENVQRIIATKETPPTSAEIASLIREQAGVISNEDIVMVLRRLRSDSVGVGPLESLLALPGVTDVLVNAHDSVWIDRGQGVEKVDMDLGSEEAVRRLATRLALTCGRRLDDAQPFADGRITRDDGSVLRIHAVLAPLAESGTCISVRVLRQARLSLDDLINSGTVPEDIAPALRNIINQRRSFLVVGGTGTGKTTLLSAMLTEVPADQRIICIEDTAELHPGHPSTINLVSRQANVEGAGAVSMADLLKQSLRMRPDRIVVGEIRGAEVVDLLAAMNTGHDGGAGTIHANSISEVPARMEALAATGGLDRMALHSQLAAAVDIVLVMKHTPFGRRLAQLGVLRGNPVTTQVVWDLDHGMHEGSEEAWFMP
>NZ_CP018175.1|WP_060563685.1|366301_367078_+|type-II-secretion-system-F-family-protein
MVYALGLLSVAVLISGSRGPGARTRPPTPGNGVHLFALIALFCLATVLFIVVEAYTMIAGIIIATTLFWYLRQTHAAAQRTKQSLQLASFLSLCAGNLRAGVTMVDAMDYALDNTTPDKFLSPTLQTAARQARSGGSGPRVLIDASLPDLQRLGHLWETSERHGIPLVALIDQMRSRISSKQRHGESTRAALQGPQATAVILTVLPLAGLLMGTAMGANPLGLLTGGGIGGFLLVIGVGLDAAGFVVTHKILQSASPS
>NZ_CP018175.1|WP_060563686.1|367074_367650_+|type-II-secretion-system-F-family-protein
MITALVIAAVAMFIGSPNPGVRGGLISPKSGKSLRIRAGPKKLGNADPVDVSADIELFSACLDAGLNTRDAAQVVAHVAAKTHRELWTHVVALLSIGVSAPQAFALMAGVDGLDELANLATVSHRSGSALSDGCRNISTSLLASAGDKRTAAAERAGVFIALPLALCFLPAFMIVGLAPVVLSLGTQLINF
>NZ_CP018175.1|WP_003855827.1|367673_367874_+|DUF4244-domain-containing-protein
MSNNLELLRLRTRAILAQDDGLTTVEYALGTLAAAALAAVLYMVVNSDAVSSAFESIISDALSARP
>NZ_CP018175.1|WP_060563687.1|367877_368198_+|hypothetical-protein
MRTKQQREPPELCSDDGSVSIEAALALSSLVIVCGLIIAAMATLAAYLAAVDAAGAAARAHAIGESFEPARGHVDMQEAGGMLTATATIPAPIGQVSASAVFPVEN
>NZ_CP018175.1|WP_060563688.1|368220_368520_+|flp-pilus-assembly-TadE/G-like-family-protein
MTIASAGVASILISLLVALAWQAGNLVAREQAQVAADVSAVAGAYAFARGELPDAACATAKHTAEANNAQLENCATEGEDLTLTVTVRGQEAHAKAGPL

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Crispr_ID: NZ_CP018175_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP018175_2

545338-545431

Orphan

Consensus_repeat	Method
AGTTTTCGGTCACCTAGTTTGGT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP018175_2

>merge|NZ_CP018175|2|545338-545431|CRISPRCasFinder
AGTTTTCGGTCACCTAGTTTGGTTTCCAACCCGCCAAACCAAACTATTTGACCGAAAATTCCCCCGGAGGCAGTTTTCGGTCACCTAGTTTGGT

>NZ_CP018175|2|2|545338-545431|CRISPRCasFinder
AGTTTTCGGTCACCTAGTTTGGT	TTCCAACCCGCCAAACCAAACTATTTGACCGAAAATTCCCCCGGAGGC
AGTTTTCGGTCACCTAGTTTGGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018175.1\|WP_060563925.1\|554539_555559_+\|porphobilinogen-synthase	unknown	unknown	gnl\|CDD\|236450
NZ_CP018175.1\|WP_060563909.1\|540109_541513_+\|MHS-family-MFS-transporter	unknown	unknown	gnl\|CDD\|340927
NZ_CP018175.1\|WP_059288679.1\|550456_551536_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270265
NZ_CP018175.1\|WP_075348086.1\|554022_554451_+\|DUF3806-domain-containing-protein	unknown	unknown	gnl\|CDD\|372263
NZ_CP018175.1\|WP_060563900.1\|535863_537258_+\|glutamyl-tRNA-reductase	unknown	unknown	gnl\|CDD\|234592
NZ_CP018175.1\|WP_003860437.1\|543889_544741_+\|quinate/shikimate-dehydrogenase-(NAD+)	unknown	unknown	gnl\|CDD\|172521
NZ_CP018175.1\|WP_075348085.1\|541536_543393_+\|dehydroshikimate-dehydratase-QsuB	unknown	unknown	gnl\|CDD\|225726
NZ_CP018175.1\|WP_060563907.1\|538949_539834_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP018175.1\|WP_060563912.1\|544746_545022_-\|50S-ribosomal-protein-L7/L12	unknown	unknown	gnl\|CDD\|223300
NZ_CP018175.1\|WP_060563917.1\|546475_547636_+\|IS3-family-transposase	unknown	unknown	gnl\|CDD\|366234
NZ_CP018175.1\|WP_065366623.1\|552209_554006_+\|bifunctional-uroporphyrinogen-III-C-methyltransferase/uroporphyrinogen-III-synthase	unknown	unknown	gnl\|CDD\|224503
NZ_CP018175.1\|WP_075348479.1\|548802_550380_-\|iron-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224099
NZ_CP018175.1\|WP_060563903.1\|537259_538168_+\|hydroxymethylbilane-synthase	unknown	unknown	gnl\|CDD\|223259
NZ_CP018175.1\|WP_040966933.1\|543438_543876_+\|type-II-3-dehydroquinate-dehydratase	unknown	unknown	gnl\|CDD\|237270
NZ_CP018175.1\|WP_075348084.1\|538661_538946_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_060563914.1\|545663_546473_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_060563926.1\|555588_556173_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_075348083.1\|535529_535778_+\|glutaredoxin-family-protein	unknown	unknown	gnl\|CDD\|368604
NZ_CP018175.1\|WP_003855576.1\|556213_556726_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_060563919.1\|547749_548802_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|226361

Protein	Function_ID	Function_description	E-value
NZ_CP018175.1\|WP_060563925.1\|554539_555559_+\|porphobilinogen-synthase	gnl\|CDD\|236450	PRK09283, PRK09283, porphobilinogen synthase.	0
NZ_CP018175.1\|WP_060563909.1\|540109_541513_+\|MHS-family-MFS-transporter	gnl\|CDD\|340927	cd17369, MFS_ShiA_like, Shikimate transporter and similar proteins of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli shikimate transporter (ShiA), inner membrane metabolite transport protein YhjE, and other putative metabolite transporters. ShiA is involved in the uptake of shikimate, an aromatic compound involved in siderophore biosynthesis. It has been suggested that YhjE may mediate the uptake of osmoprotectants. The ShiA-like subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	1.06473e-158
NZ_CP018175.1\|WP_059288679.1\|550456_551536_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|270265	cd13547, PBP2_Fbp_like_2, Substrate binding domain of an uncharacterized ferric iron transporter, a member of the type 2 periplasmic binding fold superfamily. The periplasmic iron binding protein plays an essential role in the iron uptake pathway of Gram-negative pathogenic bacteria from the Pasteurellaceae and Neisseriaceae families and is critical for survival of these pathogens within the host. This periplasmic domain (Fbp) has high affinity for ferric iron and serves as the primary receptor for transport. After binding iron with high affinity, Fbp interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The ferric iron-binding proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	6.33674e-102
NZ_CP018175.1\|WP_075348086.1\|554022_554451_+\|DUF3806-domain-containing-protein	gnl\|CDD\|372263	pfam12713, DUF3806, Domain of unknown function (DUF3806). This family represent the C-terminal domain of the structure. In two related Bacteroides species the gene lies immediately upstream from a putative ATP binding component of an ATP transporter and a putative histidinol phosphatase. The structure of this domain is strikingly similar to the N-terminal structure of 1ma7 whose C-terminal domain is a phage integrase, pfam00589.	5.71885e-22
NZ_CP018175.1\|WP_060563900.1\|535863_537258_+\|glutamyl-tRNA-reductase	gnl\|CDD\|234592	PRK00045, hemA, glutamyl-tRNA reductase; Reviewed.	7.50526e-158
NZ_CP018175.1\|WP_003860437.1\|543889_544741_+\|quinate/shikimate-dehydrogenase-(NAD+)	gnl\|CDD\|172521	PRK14027, PRK14027, quinate/shikimate dehydrogenase (NAD+).	0
NZ_CP018175.1\|WP_060563919.1\|547749_548802_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	5.01221e-128
NZ_CP018175.1\|WP_060563907.1\|538949_539834_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	6.03883e-33
NZ_CP018175.1\|WP_060563912.1\|544746_545022_-\|50S-ribosomal-protein-L7/L12	gnl\|CDD\|223300	COG0222, RplL, Ribosomal protein L7/L12 [Translation, ribosomal structure and biogenesis].	1.24501e-15
NZ_CP018175.1\|WP_060563917.1\|546475_547636_+\|IS3-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.	2.34545e-26
NZ_CP018175.1\|WP_065366623.1\|552209_554006_+\|bifunctional-uroporphyrinogen-III-C-methyltransferase/uroporphyrinogen-III-synthase	gnl\|CDD\|224503	COG1587, HemD, Uroporphyrinogen-III synthase [Coenzyme metabolism].	3.97466e-65
NZ_CP018175.1\|WP_075348083.1\|535529_535778_+\|glutaredoxin-family-protein	gnl\|CDD\|368604	pfam05768, DUF836, Glutaredoxin-like domain (DUF836). These proteins are related to the pfam00462 family.	1.36745e-13
NZ_CP018175.1\|WP_060563903.1\|537259_538168_+\|hydroxymethylbilane-synthase	gnl\|CDD\|223259	COG0181, HemC, Porphobilinogen deaminase [Coenzyme metabolism].	4.14818e-132
NZ_CP018175.1\|WP_040966933.1\|543438_543876_+\|type-II-3-dehydroquinate-dehydratase	gnl\|CDD\|237270	PRK13015, PRK13015, 3-dehydroquinate dehydratase; Reviewed.	8.40157e-84
NZ_CP018175.1\|WP_075348479.1\|548802_550380_-\|iron-ABC-transporter-permease	gnl\|CDD\|224099	COG1178, ThiP, ABC-type Fe3+ transport system, permease component [Inorganic ion transport and metabolism].	2.08141e-102
NZ_CP018175.1\|WP_075348085.1\|541536_543393_+\|dehydroshikimate-dehydratase-QsuB	gnl\|CDD\|225726	COG3185, COG3185, 4-hydroxyphenylpyruvate dioxygenase and related hemolysins [Amino acid transport and metabolism / General function prediction only].	2.06984e-132

>NZ_CP018175.1|WP_060563912.1|544746_545022_-|50S-ribosomal-protein-L7/L12
MFGRKDVNLSALEARVAALERRLAEQDRIIAQLGGDSSTPLSLQRPQSGLHPDVVALLQQGKKIAAIKRHRELTGAGLKEAKETVEASRFY
>NZ_CP018175.1|WP_003860437.1|543889_544741_+|quinate/shikimate-dehydrogenase-(NAD+)
MNDSILLGLIGQGLDLSRTPAMHEAEGLAQGRATVYRRIDTLGSRASGQDLKTLLDAALYLGFNGLNITHPYKQAVLPLLDEVSEQATQLGAVNTVVIDANGHTTGHNTDVSGFGRGMEEGLPNAKLDSVVQVGAGGVGNAVAYALVTHGVQKLQVADLDTSRAQALADVINNAVGREAVVGVDARGIEDVIAAADGVVNATPMGMPAHPGTAFDVSCLTKDHWVGDVVYMPIETELLKAARALGCETLDGTRMAIHQAVDAFRLFTGLEPDVSRMRETFLSL
>NZ_CP018175.1|WP_040966933.1|543438_543876_+|type-II-3-dehydroquinate-dehydratase
MPGKILLLNGPNLNMLGKREPDIYGHDTLEDVVALATAEAAKHGLEVEALQSNHEGELIDALHNARGTHIGCVINPGGLTHTSVALLDAVKASELPTVEVHISNPHAREEFRHHSYISLAAVSVIAGAGIQGYRFAVDILANLQK
>NZ_CP018175.1|WP_075348085.1|541536_543393_+|dehydroshikimate-dehydratase-QsuB
MRTSIATVCLSGTLAEKLRAAADAGFDGVEIFEQDLVVSPHSAEQIRQRAQDLELTLDLFQPFRDFEGVEEEQFLKNLHRLEEKFKLMNRLGIEMILLCSNVGTATINDDDLFVEQLHRAADLAEKYNVKIAYEALAWGKFVNDFEHAHALVEKVNHKALGTCLDTFHILSRGWETDEVENIPAEKIFFVQLADAPKLSMDILSWSRHHRVFPGEGDFDLVKFMVHLAKTGYDGPISLEIFNDSFRKAEVGRTTIDGLRSLRWLEDQTWHALNAEDRPSALELRALPEVAEPEGVDFIEIATGRLGETIRVLHQLGFRLGGHHCSKQDYQVWTQGDVRIVVCDRGATGAPTTISAMGFDTPDPEAAHARAELLRAQTIDRPHIEGEVDLKGVYAPDGVELFFAGPSPDGMPEWLPEFGVEKQEAGLIEAIDHVNFAQPWQHFDEAVLFYTALMALETVREDEFPSPIGLVRNQVMRSPNDAVRLLLSVAPEDGEQGDFLNAAYPEHIALATADIVAVAERARKRGLDFLPVPENYYDDVQARFDLPQEFLDTLKENHLLYDRDENGEFLHFYTRTLGTLFFEVVERRGGFAGWGETNAPVRLAAQYREVRDLERGIPN
>NZ_CP018175.1|WP_060563909.1|540109_541513_+|MHS-family-MFS-transporter
MSEQLQGVTHSESTPGKTPKRAALSSWIGSALEYYDFAVYGTAAALVLNHLFFPADTSPGIAILAAMGTVGVAYVVRPLGALIMGPLGDRYGRKFVLMLCLFLIGASTFAVGCLPTFDQVGYLAPALLVLCRVIQGLSASGEQSSAISVSLEHADERHRAFTASWTLHGTQFGTLLATGVFIPFTLFLSEDALMSWGWRVPFWLSAAVVLVAFLIRRGLEEPPAFHENKEAVAGAASPLAMTLRYHKAAVVRVAIAAMINSVNIVFTVWALSFATNIVGLDRSTVLLVPVVANLVALIAIPLSGMLADRIGRRPVFIMGAIGGGLAMNGYLGAIYSGNWTMIFFMGVLMSGLLYSMGNAVWPAFYAEMFPTSVRVTGLALGTQIGFAVSGGFVPVIASALAGDQGDQWMKVSIFVGVVCVISALVAMTAKETKALTLDEIDALHTARGEAADLAAASKASEAQLAAQ
>NZ_CP018175.1|WP_060563907.1|538949_539834_-|LysR-family-transcriptional-regulator
MHLNQLEFFIAVAQHGQINRAAEDLLISQPALSRQISALEKSVGAPLFERHSRGVSLTKAGEILHEEALRTLSRMQSVVDEIQSGEHLITSINIGVPPGIPIDWLRCQLIDLGPETRISLIESPTDDQLKLLKQRELDIALCRRQSEAFATTLVHEQELGIVVRKNSELHQKVAGKDNATLFDLEGLRVLAHSRGEVRIQEEILKNAMLAAGVNATWIFRKFGQYSSLIADLVQADVALTTEESARTNFPSWQWVPIEGEDASGNDLVVRTWITWNPQPTPAVKALIQKFIDGN
>NZ_CP018175.1|WP_075348084.1|538661_538946_+|hypothetical-protein
MRIPRKAIRNIQVVDNVISSVDRPIKRAGRLRIPGVFVAGTHAYVNETLSENEFSMCRKNEPGLVIELENISIDRIVISTPDAHRYADELMAAV
>NZ_CP018175.1|WP_060563903.1|537259_538168_+|hydroxymethylbilane-synthase
MTLKIGTRGSKLATTQAGTIRDQLKHYGRDAELHIVTTPGDVNMSPVERIGVGVFTQALRDVLHSGDCDVAVHSMKDLPTAADPRFHLVVPTRADSREALIARDGLTLAELPEGAKVGTSAPRRISQLKVIRPDLEILPLRGNIDTRMGKVTSGELDAVMLAYAGLTRVGMQDRATEVFDADIIMPAPAQGALAIECRADDTETVRALNMLMHADTFVSAVAERTVLNRLEAGCTAPVAAHATLDGYSGDTMTLTAGVYALDGSDQLVFSAEGDGARPEELGELVAQQLIDAGAANLLGDRS
>NZ_CP018175.1|WP_060563900.1|535863_537258_+|glutamyl-tRNA-reductase
MVSVLIVGMSHRSAPVSLLERLSMDDSVRGETTQALLGRASLSEALIVSTCNRLEVYTVTSSFHTGVNDVVEVLHEASGVDIETLRGYLYVRYADAAAEHMLVVTSGLDSMVLGEQQIIGQVRTAYQAANEYGSVGPALHSLTQTALHTGKRVHSETAIDDAGASMVSFAVDRALVQMGLDPEAEAPLSGKTALVLGAGAMSSLAATHLGRAGISNLIMANRTLERAERLAEHSLEAGVPAEVVEYDQRASAYNRVDLVVSATGADDFTVKPEDIPEGASLMLVDLSMPRDIDDACADLPGVDLVNIERLHKASREGGSGMAPSEEEALAIVREELDSFTSEQRIRDIVPAVSALRRQAASVGSDELDRLRQRAPGISEVEWGEVEKTVRRVVDKLLHEPTVRVKELAARSGSISYDSALQELFGLESLASTAAPATTSVNASELPDAGIVAFVNAPSATQTRE
>NZ_CP018175.1|WP_075348083.1|535529_535778_+|glutaredoxin-family-protein
MGATMGHSVEIIVRDNCGSCVRVKAQILSIVEAAGIKLTERNVDQDASLKLEFGDRVPVILVDDEEFACWEVDNDELANALL
>NZ_CP018175.1|WP_060563914.1|545663_546473_+|hypothetical-protein
MSIPFSVLQDYLDLISPEALPQIPQPPAPAPTAPQLPPAPDPHSIEWPIFPPDRISANGRRYYEPQTRLEFMRIYTTLPHGYRQPFLKANNIGHCTVRTWLAAISTFSRLPHAFDDAHRFGIERTTPVDDVTTLTADDKRDLVIGYLAQPHGQGQQFLTFYQLRKHTIMAWCAAMTDGDLDADVYPRKIGLMTTRTVVEIVRLRHMIAQQLERATIMENEYLKEIAALKKELAHYKQKDHQNQMVIDILGKAIGTRPNPGEGLDEEDAT
>NZ_CP018175.1|WP_060563917.1|546475_547636_+|IS3-family-transposase
MDEQRAFDQGLKEENTLITDLTTCARLSHNKALRLIKLSKSTAYYRNKPRPCPAPKPVLQAVAAPTAPGVEPTPEPWQGKEPAVSSVRQALAEHERQFIVDAITAYPQLSVSGVFNMLFNKGIYRASLRTWWRVAKQHKLLHKDRVSALSPGKRSPTPRVKPRLEATQPGQVVCWDVTFLPSLVRGKTYALHLAIDLFSRKIVGAKVAPTENTSTAVELLTQVLADNPGVVTVHSDNGSAMTSTRVRRLLADHGVALSLIRPRVSDDNAFVESVFHTLKYRPFYPKVFASMDQARVWVEEFVVYYNTVHPHSGVAGHTPQSVFDGSWRAAHRLRVQALDAHYRQFPQRYVGRPVVQEVAGVVRLNGARDDGSVQERVGGVASLLSA
>NZ_CP018175.1|WP_060563919.1|547749_548802_-|ABC-transporter-ATP-binding-protein
MSSIKLRDLSVSFRDGTFGLLDINLKIEPEEFVVLIGPSGSGKTTMLRTIAGFAEPTSGSVLIGGEDMTHVPPERRRMGMVFQQHAVWPHMSVAKNVGYPLARSGQKGASISKRVERTLALVGLEGFGSRKPASLSGGQRQRVALARAIIADPTVLLLDEALSALDEPLRDALRRELVSLTRREGLTTVHVTHDRAEAISIADRIVVLGNGRIQQVATPTELLSAPATADVARFIIDATVLNGIVRNGRVMCPDLDTSWDLDAVQAIDDIFDGDLVDIAIPPHSVGIGPAHHPDYIFAEITSVLFQVTSYSVTAKTQSGHSFRMSITCSVPEIGETIGLSIDNPMVYRAD
>NZ_CP018175.1|WP_075348479.1|548802_550380_-|iron-ABC-transporter-permease
MRLGVWLIVAGLFITPLALVVGLALGGNQFPALWDSGLGKALWNSAYTTVLSAVGATIIGTIMALTLDRTDVFGRTALRLFLLSPLLIPPFIGAIAWLQLFGKNQGINRFFGTEVWDIYGADGVTFLLIVHSYPTVYIIVSAALRQLPSDLEQAARIAGADTFTVLRTITLPLLKPALLSAFTLTAVANLADFGIPALLGSPARFETLATMIYRFMESGTVSNPLQVVSTIGIVLLFLGIAAVTADYLVSLYAASKLQDAGTPHRFTLNKSRIPVSLITWIIALIITAAPLLGLAYRALLPAPGVPFNLDNITLNNFEAALSNPRVIEGFSNSLMLSLGAALICGVLGWLIGVLITRTQHFANVPLTLTVLLPTALPGMIIGVGWLILGRYTGIYNTPWVILGAYVCAFTALVVQAVRGPLSQAPEAIEEAARISGAGRLRSIMDTTGAMAIPAAFAGAVLVAVTAVRELTVSILLIAPGTTTLGVQVFNLQQAGNYNQASALSLMFAIIGIVALALTVRSQKEF
>NZ_CP018175.1|WP_059288679.1|550456_551536_-|ABC-transporter-substrate-binding-protein
MSSKHPLKRTAVTVFALGASAALLVACSEPSEDVSTAETTTASSSANASDAAGEKVTITVYTSEPEEKVDEINKAFMEANPDIEVEVYRAGTGDLTARIEAEKASGSIEADVLWAADAATFETYAAQGDLAELEDVDTSDIIEEALDAENFYVGTRIIPTVIAYNTEVVDQAELPTSWADLTDPKYAGQLVMPDPAVSGAAAFNASVWKNDPALGEAWITALGENQPMIAQSNGPTSQEIAGGGHPVGIVVDYLVRDLAAAGSPIDTIYASEGSPYITEPAGVFADSEKKEAAERYINFLLSVEGQEIAVEQAYLPVREDVGTPEGTPELADIELMTPDLEVVTADKAAAVEFFQNAMN
>NZ_CP018175.1|WP_065366623.1|552209_554006_+|bifunctional-uroporphyrinogen-III-C-methyltransferase/uroporphyrinogen-III-synthase
MTIAHKPEMAETTGIETNQVSETIGVESLTHGNLRPVSSFEGQHEGQTEELLPGKVIFVGAGPGNPDLLTVRAREVLGNAVRAITDEQVLSGVRAFVATEIPVPEDKLQAAEDEYERICIEAKENGARRKPPRPAPPTAAEITEVSEATPAQIVELVQDALSYGGDVIRLVTGNPLSSDATLAEISAVSEAGLEFQVVPGMSLPGTVPAFAGIALGSTYTETDVNGQDLDWDQLASAPQPLVLQARVDDLSRIAQELKARNMSLETPVSVTVNGTTRLQRTYDTTLGLLHKLDAELSGPLVVTLGKGVDDRSKYSWWENRALYGWRVLVPRPREQAASMSARLSSHGAIPQEVPTISVEPPRNPAQMERAIKGIVEGRYQWVVLTSVNAVKAVWEKITEFGLDSRSFAGVRIAAVGEKTAAEIRALGITPELLPARTRQNAQGLVDVFPEYFEELDPVGRVLLPRADIATDVLVDGLTHLGWEVEDVVAYRTVRAAPPSADIRDMIKTGGFDAVAFTSSSTVKNLVGIAGKPHPRTIVACIGPMTAATAEELGLRVDVMPEIAEVPELIDALAEHVADLRAKGELPPPRKKRRRRKAS
>NZ_CP018175.1|WP_075348086.1|554022_554451_+|DUF3806-domain-containing-protein
MLSMDIQQLDAETTAWKDSLLRAAQEAGFHFEPPKFFEDFETMVEQYKQAAASDPDIDVTDIQQMWGIVVGEYLREKMGMEWVVITDDYGTDLAILATAPNGDHVYSCPIIVVGKRFSTDYEPGQLEFFCNQFMVTSLAQLQ
>NZ_CP018175.1|WP_060563925.1|554539_555559_+|porphobilinogen-synthase
MSTSSDYSHALIRRPRRLRANPAMRELVAETALRPADLILPMFFADGIAEAREISSMPGVYQHTEDSLLRAAHEALDAGVRCVDLFGVPVDAAKDFNGSEAWSETGVLNRALSSLRKEFGDDLLIMADTCLDEFTDHGHCGVVTEDRHGNAIVDNDATLPLYQQMAVAQARAGAHIVSPSGMMDGQIAAIRAALDEEGYQDVAIMAYSAKYASAFFGPFREAVGSSLQGDRRTYQQDPANLRESLLEAELDIAEGADFIMVKPALPYLDVLTRIADTSPVPVAAYQVSGEYAMIQAAGRNGWVDLDAVMMESLTSIKRAGANQILTYFAVNAARALRNA
>NZ_CP018175.1|WP_060563926.1|555588_556173_+|hypothetical-protein
MSMLPNLTPKKSAPPSSSASAKNPGEKKEDTVKLLIQMWAVMIGLELLHQILNVVMSFTDPTALRTVAKEQAAAQGLSDGIVNATVIAAILVMGFFNLIVIAILSWMVVMVKNRSKRLPTAFLLLTIFSFFFILRVLMLFFASPGGTDVPMALFAIDGCVQILVGVSAGVAYALSRTEQPVKMLTDYAPEDAKR
>NZ_CP018175.1|WP_003855576.1|556213_556726_+|hypothetical-protein
MPSMFPSPATGGDDINRRPLNEPNADATTIPTALKVVFWMLFATAAFMIFTGLVMYTAGYTGPDDVDESYKAVVVNNQEFIGGINAFAGIVIAALTSQLPKGGKNPRRLLLAIMLLVLLTDLLSFATRAGGFALAIIAVLLALEALLMFRPAVNDHIDRNHMARVMNREK

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Crispr_ID: NZ_CP018175_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP018175_3

2912992-2913077

Orphan

Consensus_repeat	Method
AGGTGGCTTTTAGAGGGACCGACT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP018175_3

>merge|NZ_CP018175|3|2912992-2913077|CRISPRCasFinder
AGGTGGCTTTTAGAGGGACCGACTTACCCATCGCCCGCGTCACTCATGACCGAACTCAAAGAAGGTGGCTTTTAGAGGGACCGGCT

>NZ_CP018175|3|3|2912992-2913077|CRISPRCasFinder
AGGTGGCTTTTAGAGGGACCGACT	TACCCATCGCCCGCGTCACTCATGACCGAACTCAAAGA
AGGTGGCTTTTAGAGGGACCGGCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018175.1\|WP_060565527.1\|2919789_2920722_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213235
NZ_CP018175.1\|WP_003853704.1\|2906963_2908094_-\|glutamate--cysteine-ligase	unknown	unknown	gnl\|CDD\|237408
NZ_CP018175.1\|WP_074492444.1\|2920743_2921247_-\|NUDIX-hydrolase	unknown	unknown	gnl\|CDD\|239217
NZ_CP018175.1\|WP_003853711.1\|2905541_2905922_+\|cation:proton-antiporter	unknown	unknown	gnl\|CDD\|183613
NZ_CP018175.1\|WP_060565238.1\|2913361_2914558_-\|multidrug-effflux-MFS-transporter	unknown	unknown	gnl\|CDD\|340878
NZ_CP018175.1\|WP_075348376.1\|2919038_2919809_-\|multidrug-ABC-transporter-permease	unknown	unknown	unknown
NZ_CP018175.1\|WP_060565239.1\|2917031_2918198_+\|Na/Pi-cotransporter-family-protein	unknown	unknown	gnl\|CDD\|224202
NZ_CP018175.1\|WP_003853699.1\|2908833_2909046_-\|DUF3263-domain-containing-protein	unknown	unknown	gnl\|CDD\|378688
NZ_CP018175.1\|WP_075348375.1\|2918194_2919037_-\|PhzF-family-phenazine-biosynthesis-protein	unknown	unknown	gnl\|CDD\|223461
NZ_CP018175.1\|WP_003862899.1\|2905265_2905541_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|181179
NZ_CP018175.1\|WP_075348373.1\|2909632_2910640_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|366181
NZ_CP018175.1\|WP_075348530.1\|2921441_2922830_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_075348374.1\|2915846_2916656_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP018175.1\|WP_060565237.1\|2911464_2912967_+\|cardiolipin-synthase-A	unknown	unknown	gnl\|CDD\|234967
NZ_CP018175.1\|WP_038586019.1\|2922830_2923865_+\|glutamate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270408
NZ_CP018175.1\|WP_003862894.1\|2909061_2909643_+\|peptide-deformylase	unknown	unknown	gnl\|CDD\|237227
NZ_CP018175.1\|WP_060563917.1\|2914683_2915844_-\|IS3-family-transposase	unknown	unknown	gnl\|CDD\|366234
NZ_CP018175.1\|WP_003853708.1\|2906357_2906957_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP018175.1\|WP_003853692.1\|2910666_2911458_+\|exodeoxyribonuclease-III	unknown	unknown	gnl\|CDD\|197320
NZ_CP018175.1\|WP_003853702.1\|2908162_2908828_-\|LytR-C-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|379163

Protein	Function_ID	Function_description	E-value
NZ_CP018175.1\|WP_060565527.1\|2919789_2920722_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|213235	cd03268, ABC_BcrA_bacitracin_resist, ATP-binding cassette domain of the bacitracin-resistance transporter. The BcrA subfamily represents ABC transporters involved in peptide antibiotic resistance. Bacitracin is a dodecapeptide antibiotic produced by B. licheniformis and B. subtilis. The synthesis of bacitracin is non-ribosomally catalyzed by a multi-enzyme complex BcrABC. Bacitracin has potent antibiotic activity against gram-positive bacteria. The inhibition of peptidoglycan biosynthesis is the best characterized bacterial effect of bacitracin. The bacitracin resistance of B. licheniformis is mediated by the ABC transporter Bcr which is composed of two identical BcrA ATP-binding subunits and one each of the integral membrane proteins, BcrB and BcrC. B. subtilis cells carrying bcr genes on high-copy number plasmids develop collateral detergent sensitivity, a similar phenomenon in human cells with overexpressed multi-drug resistance P-glycoprotein.	1.28038e-94
NZ_CP018175.1\|WP_003853704.1\|2906963_2908094_-\|glutamate--cysteine-ligase	gnl\|CDD\|237408	PRK13517, PRK13517, glutamate--cysteine ligase.	0
NZ_CP018175.1\|WP_074492444.1\|2920743_2921247_-\|NUDIX-hydrolase	gnl\|CDD\|239217	cd02883, Nudix_Hydrolase, Nudix hydrolase is a superfamily of enzymes found in all three kingdoms of life, and it catalyzes the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+ for their activity. Members of this family are recognized by a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolase include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance and "house-cleaning" enzymes. Substrate specificity is used to define child families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required. This superfamily consists of at least nine families: IPP (isopentenyl diphosphate) isomerase, ADP ribose pyrophosphatase, mutT pyrophosphohydrolase, coenzyme-A pyrophosphatase, MTH1-7,8-dihydro-8-oxoguanine-triphosphatase, diadenosine tetraphosphate hydrolase, NADH pyrophosphatase, GDP-mannose hydrolase and the c-terminal portion of the mutY adenine glycosylase.	4.6603e-16
NZ_CP018175.1\|WP_003853711.1\|2905541_2905922_+\|cation:proton-antiporter	gnl\|CDD\|183613	PRK12592, PRK12592, putative monovalent cation/H+ antiporter subunit G; Reviewed.	2.61795e-74
NZ_CP018175.1\|WP_060565238.1\|2913361_2914558_-\|multidrug-effflux-MFS-transporter	gnl\|CDD\|340878	cd17320, MFS_MdfA_MDR_like, Multidrug transporter MdfA and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as MdfA (also called chloramphenicol resistance pump Cmr), EmrD, MdtM, MdtL, bicyclomycin resistance protein (also called sulfonamide resistance protein), and the uncharacterized inner membrane transport protein YdhC. EmrD is a proton-dependent secondary transporter, first identified as an efflux pump for uncouplers of oxidative phosphorylation. It expels a range of drug molecules and amphipathic compounds across the inner membrane of E. coli. Similarly, MdfA is a secondary multidrug transporter that exports a broad spectrum of structurally and electrically dissimilar toxic compounds. These MDR transporters are drug/H+ antiporters (DHA) belonging to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.30364e-100
NZ_CP018175.1\|WP_060565239.1\|2917031_2918198_+\|Na/Pi-cotransporter-family-protein	gnl\|CDD\|224202	COG1283, NptA, Na+/phosphate symporter [Inorganic ion transport and metabolism].	4.15863e-96
NZ_CP018175.1\|WP_003853699.1\|2908833_2909046_-\|DUF3263-domain-containing-protein	gnl\|CDD\|378688	pfam11662, DUF3263, Protein of unknown function (DUF3263). This family of proteins with unknown function appears to be restricted to Actinobacteria.	3.49121e-25
NZ_CP018175.1\|WP_075348375.1\|2918194_2919037_-\|PhzF-family-phenazine-biosynthesis-protein	gnl\|CDD\|223461	COG0384, COG0384, Predicted epimerase, PhzC/PhzF homolog [General function prediction only].	1.89268e-100
NZ_CP018175.1\|WP_003862899.1\|2905265_2905541_+\|hypothetical-protein	gnl\|CDD\|181179	PRK07948, PRK07948, putative monovalent cation/H+ antiporter subunit F; Reviewed.	4.78942e-38
NZ_CP018175.1\|WP_075348373.1\|2909632_2910640_+\|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.	2.80971e-10
NZ_CP018175.1\|WP_060565237.1\|2911464_2912967_+\|cardiolipin-synthase-A	gnl\|CDD\|234967	PRK01642, cls, cardiolipin synthetase; Reviewed.	4.27935e-117
NZ_CP018175.1\|WP_038586019.1\|2922830_2923865_+\|glutamate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|270408	cd13690, PBP2_GluB, Substrate binding domain of ABC glutamate transporter; the type 2 periplasmic binding protein fold. This group includes periplasmic glutamate-binding domain GluB from Corynebacterium efficiens and its related proteins. The GluB domain belongs 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.	3.78811e-75
NZ_CP018175.1\|WP_003862894.1\|2909061_2909643_+\|peptide-deformylase	gnl\|CDD\|237227	PRK12846, PRK12846, peptide deformylase; Reviewed.	6.52209e-77
NZ_CP018175.1\|WP_060563917.1\|2914683_2915844_-\|IS3-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.	2.34545e-26
NZ_CP018175.1\|WP_003853708.1\|2906357_2906957_-\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	1.28371e-06
NZ_CP018175.1\|WP_003853692.1\|2910666_2911458_+\|exodeoxyribonuclease-III	gnl\|CDD\|197320	cd09086, ExoIII-like_AP-endo, Escherichia coli exonuclease III (ExoIII) and Neisseria meningitides NExo-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes Escherichia coli ExoIII, Neisseria meningitides NExo,and related proteins. These are ExoIII family AP endonucleases and they belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER, the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiencies. Many organisms have two AP endonucleases, usually one is the dominant AP endonuclease, the other has weak AP endonuclease activity. For example, Neisseria meningitides Nape and NExo, and exonuclease III (ExoIII) and endonuclease IV (EndoIV) in Escherichia coli. NExo and ExoIII are found in this subfamily. NExo is the non-dominant AP endonuclease. It exhibits strong 3'-5' exonuclease and 3'-deoxyribose phosphodiesterase activities. Escherichia coli ExoIII is an active AP endonuclease, and in addition, it exhibits double strand (ds)-specific 3'-5' exonuclease, exonucleolytic RNase H, 3'-phosphomonoesterase and 3'-phosphodiesterase activities, all catalyzed by a single active site. Class II AP endonucleases have been classified into two families, designated ExoIII and EndoIV, based on their homology to the Escherichia coli enzymes ExoIII and endonuclease IV (EndoIV). This subfamily belongs to the ExoIII family; the EndoIV family belongs to a different superfamily.	1.12558e-104
NZ_CP018175.1\|WP_003853702.1\|2908162_2908828_-\|LytR-C-terminal-domain-containing-protein	gnl\|CDD\|379163	pfam13399, LytR_C, LytR cell envelope-related transcriptional attenuator. This family appears at the C-terminus of members of the LytR_cpsA_psr, pfam03816, family.	0.0014775

>NZ_CP018175.1|WP_060565237.1|2911464_2912967_+|cardiolipin-synthase-A
MIFQINLESWQTVGLIIDYTIKIIAIGYVPEGRRPSSSTAWLLAILLLPYVGLPLFLLMGSPYINRRRHRIQQEINDLIEDVHDDVPDIPTGMDVSAEVESVIKLNRRLTRMPAVTGGNNGFYSDYRESLKRMTAAIDEAEEYIYVEIYIMAWDSCTQPFFAALERAHNRGVQVRLLFDHVGSWKYPGYHRLKKELNRMGFAWYLMLPLQPWRRRFRRPDLRNHRKMLIIDGHTAFMGSQNLIAPSYLQKKNIKLGREWKDLMVELTGPIVSSMEMIFAGDWYVESNEALDIRDHAEAHGYIGNTQKDSATNLVQLIPSGPGYTTEPNLRMFNSIVHHAKERLILCSPYFIPDESLLEAVTSACYRGVTVELFVSEQADQFAIDHAQSSYYQALLEAGVKIYQFPKPDVLHTKYMIADPDDTTGNEALGVLGSSNLDIRSFGLNYEISLMIAKGNLIHELNALTDRYRTVSLKLTLDKWNQRSWRRRYVDNVMRLTSALQ
>NZ_CP018175.1|WP_003853692.1|2910666_2911458_+|exodeoxyribonuclease-III
MRIVNWNVNSARTRVDRMVDFLLRHDVDVLAVQETKCKDEQFPTERFTEIGYEVAHFGLNQWNGVAIISRVGIENVETHFPAQPGFNKDITKEQSIEARAIGARCGGVQVWSLYVPNGREIADPHYDYKLRWLFSLRNYVIDTLEYRPEEKLVLLGDFNIAPTDIDVWDIAAFEGKTHVTEPERAAFDGLIEAGLKETTPGPGTYTYWDYKGARFLKGEGMRIDFQLASPALAATAGETFVDVEERSGTGASDHAPVIVDYKV
>NZ_CP018175.1|WP_075348373.1|2909632_2910640_+|GNAT-family-N-acetyltransferase
MTPSLPRFRSQKPAVGDRVVARRRIPGANVHWTDAIGHVIGVDPLVVRPQSVGGMPSDAEEIVIPDDQLEVIKILSPRTIRNSDIRAVEVATAKAFPGLVNEWHDGWLLRAGDGIAERSNSASPLGPSVGFEPVPMEDISRFYARHDLPVKLHIPERIGRPAQKVIDADPQKWVMGPEILVMTKSLDHVESHELPGGLEFSVDKQPDQEWLGMYHFRGQALPAHALELLRTQIEGRMGFGRLTTPAGQTVAITRATITAAEEHIFLGYSAVEVDPAFRRQGLGTALGSRIQEWGAEQHAQEAYLQVVAHNEAGIGLYQKLGFSEHHRHRYAERKF
>NZ_CP018175.1|WP_003862894.1|2909061_2909643_+|peptide-deformylase
MTVRPIVIHGDPVLHNPTQLVTEDVSELQELIADMYETMDVANGVGLAANQIGVSKRIFVYDCPDDEGVMHKGCFINPVLETSEIPETMPADDGSDEEGCLSVPGEGFPTGRAHWAKVTGLNEKGEEVSVEAEGFLARCFQHEVGHLDGFLYTDVLIGRWKRMAKKAIKANGWTEPGLTWMPGEDEDPFGHDA
>NZ_CP018175.1|WP_003853699.1|2908833_2909046_-|DUF3263-domain-containing-protein
MLSADDLTLLEFEAHAPHAIGAKEEAIRATFGISPVRYYQRLNVIIDTPEAMKVNPTLVSRLRRRAGKID
>NZ_CP018175.1|WP_003853702.1|2908162_2908828_-|LytR-C-terminal-domain-containing-protein
MTSDMQNSPQHSATPSEEKQGGLPMRGLAMILIAVAVLLAAWALWSMQGKDDTSTTSAGQTQSTETNAGTIAESSGSSDSEQASAEPGTSEETSAEQPAADGEAANAAGTAAAGGASSANGNSTPVNTLYVLNNSTVPQLAARVADSLSGDYQKVESGNLPDTIIPQNTVYFTAGNTEAEKAARELADRVSGVAMERSDALPTETEGKDALVLVLVQDVAL
>NZ_CP018175.1|WP_003853704.1|2906963_2908094_-|glutamate--cysteine-ligase
MGIEFKRSPRPTLGVEWEIALVDPETRDLAPRAAEILEIVAKNHPEVHLEREFLQNTVELVTGVCDTVPEAVAELSHDLDALKEAADSLGLRLWTSGSHPFSDFRENPVSEKGSYDEIIARTQYWGNQMLIWGIHVHVGISHEDRVWPIINALLTNYPHLLALSASSPAWDGLDTGYASNRTMLYQQLPTAGLPYQFQSWDEWCSYMADQDKSGVINHTGSMHFDIRPASKWGTIEVRVADSTSNLRELSAIVALTHCLVVHYDRMIDAGEELPSLQQWHVSENKWRAARYGLDAEIIISRDTDEAMVQDELRRLVAQLMPLANELGCARELELVLEILERGGGYERQRRVFKETGSWKAAVDLACDELNDLKALD
>NZ_CP018175.1|WP_003853708.1|2906357_2906957_-|alpha/beta-hydrolase
MVESQHIIFIPESQQTPDEFTEVVNEIPAGIKPRIVPWSGSVSAGVQAVESILDREEIRRVILVGAGTGAGVALEIAKNQPRRVERLVLDSPLVTFDEKQLKGMSTALKMMPGFFFRKKNKKDLLQQVEEARTAVPMGFSEITMPTLIIRGSAAKAGIDSDLEKQIPSARATTIIGANWLTYTTHGRQTGAAIAEFLAQ
>NZ_CP018175.1|WP_003853711.1|2905541_2905922_+|cation:proton-antiporter
MTLQLFTDIVSLVFILSGAFLSFSASIGLIRFKDTMSRVHAMTKPQTTGLILTVVGAIIRILGHEHFDQSQRSDLGVLVLLVLFALLTSPVTAQRVGRVSRREGLYGAKDDMSDNQAPAELKPKKS
>NZ_CP018175.1|WP_003862899.1|2905265_2905541_+|hypothetical-protein
MDNTLYTAGLTIAAAFFMLSFIFTIYRIIVGPNSIDRLLGLDGTVSMIQCSMATYICWTLDTTVTNFMMVIALLGFISSVSVARFRKRDGA
>NZ_CP018175.1|WP_060565238.1|2913361_2914558_-|multidrug-effflux-MFS-transporter
MQKKQQLSTALIMGLALLSASSALATDMYLPAMPGIAEDLGTTAPMVQLTLSSFMAGMAIGQLIIGPLSDQLGRKGLLVAGAVAALVASVVCALAPSISVLVIARLVQGLGGGACVVIARAIVPDLERGQKAAHAFALLMIIQGIAPVVAPLIGGVLVGPFGWRGIFWALALVNFAQLLVALLQIKESKPVEERTAAGLGGMLSNYVFVLKNPQFLAYVFTLGLSFGAMFSYISASPFVLQNQMGIPVLLYSIIFGVNAFGLIVGGMVNRRLLQRIHPHRIMQTVLASFTVLCALLLIEVLFINWIPLFLVLLFLIVSHIPMVMANATALGTEVVRSRAGSGSAILGFVQFTMGALVSSLVGLGSDKALTMGIAMTACALLACGCAYLAGRKGIPEMK
>NZ_CP018175.1|WP_060563917.1|2914683_2915844_-|IS3-family-transposase
MDEQRAFDQGLKEENTLITDLTTCARLSHNKALRLIKLSKSTAYYRNKPRPCPAPKPVLQAVAAPTAPGVEPTPEPWQGKEPAVSSVRQALAEHERQFIVDAITAYPQLSVSGVFNMLFNKGIYRASLRTWWRVAKQHKLLHKDRVSALSPGKRSPTPRVKPRLEATQPGQVVCWDVTFLPSLVRGKTYALHLAIDLFSRKIVGAKVAPTENTSTAVELLTQVLADNPGVVTVHSDNGSAMTSTRVRRLLADHGVALSLIRPRVSDDNAFVESVFHTLKYRPFYPKVFASMDQARVWVEEFVVYYNTVHPHSGVAGHTPQSVFDGSWRAAHRLRVQALDAHYRQFPQRYVGRPVVQEVAGVVRLNGARDDGSVQERVGGVASLLSA
>NZ_CP018175.1|WP_075348374.1|2915846_2916656_-|hypothetical-protein
MSIPFSVLQDYLDLISPEALPQIPQPPAPAPTAPQLPPAPDPHSIEWPIFPPDRISANGRRYYEPQTRLEFMRIYTTLPHGYRQPFLKANNIGHCTVRTWLAAISTFSRLPHAFDDAHRFGIERTTPVDDVTTLTADDKRDLVIRYLAQPHGQGQQFLTFYQLRKHTIMAWCAAMTDGDLDADVYPRKIGLMTTRTVVEIVRLRHMIAQQLERATIMENEYLKEIAALKKELAHYKQKDHQNQMVIDILGKAIGTRPNPGEGLDEEDAT
>NZ_CP018175.1|WP_060565239.1|2917031_2918198_+|Na/Pi-cotransporter-family-protein
MLLSGWGKFVRWLLVLLSILVIIIGINLILDGVYGFGTFSTTQMYQVAKDPLIGVLIGILATALVQSSTTTTTLTVTAVGTGIVSVPVAIPIILGANIGTTITAMLVAFSYVGERREFKRAFTVAAMHVWFNVLVILVLFVVELLFHPFRTISGAIATEITLTTGGSLPTSDVMTKIFDPPTQLLGMNGLIGSIGNPSISAIVCLVVGTILILISVRAMSSQIRTITAATVTSIMDKVINPENSPKATILSNFWSFILGVLFTLMVTASSVTVASMQPVAVSGVVKQKPLLGVILGANVGTTVTAMFATFAIVSDQGEFAIQAALIHLIVNFTGALLVLCIPQLANVIIHLAEKTANLTARSYSITLATIVTAYVLVPSAVLMIYFFI
>NZ_CP018175.1|WP_075348375.1|2918194_2919037_-|PhzF-family-phenazine-biosynthesis-protein
MPSKISRPYYQVDVFSSEPFMGNPLAVIADADDLSAEQMARIARWTNLSETTFLLKPTQEGADYRVRIFTPTGELPFAGHPTLGTAHVFRELHGEQGTQLVQECVAGLVAVRAIDGPASGLAFQAPPTLKDGPLDASDLDAACEALGISPDFIRAHQWVDNGPGWAVVELPSAQHVLDLEPDFSAHPTLKLGVIGAYPEGAPHAFEVRAFAPGIGEDPVTGSLNASIAQWLHRDGRAGEGYLASQGTAIGRVGEIHISIESHVIWVGGSVTTIFQGTAEF
>NZ_CP018175.1|WP_075348376.1|2919038_2919809_-|multidrug-ABC-transporter-permease
MWTTMINTIRSEWTKLVTTKSFWWTTALILVFSLGYAALTESLATGESFASLFLLAGSTVTGLYLLGFVVIMIQSIMMFTTEFRFGYQTQTFLATPKRWVVAVSKWLLYLVFAVVLTFITVILCFYLAKALASDTASSTLVVWEDTQARRIMWQYPLAAALLVTFCSGIALLLRQTAGAVALVLMWHFAIENLLSFLPRIGEYVGKYGPFTNLYAFITDYQSIDPGWSTTMGAVYFGAWAFVLFALGIVVLEKKDA
>NZ_CP018175.1|WP_060565527.1|2919789_2920722_-|ABC-transporter-ATP-binding-protein
MINVEGLTKQYGQVRAVDDLSFEVKPGIVTGFLGPNGAGKSTTMRLILGLDNPTAGHATIEGQPYRSLKNPLTKVGALLDAKATHPNRTAENHLKWIARANGLSTKRVDEVLTLVGLTGVASKKTGGFSLGMGQRLGLAAALLGDPEYLILDEPVNGLDPEGIHWVRTLLQNIAKQGRTVLVSSHLLSEMAQTAEHLIVIGRGKLVADMPMHEFVRSHSASTVVVRAAVPGALESALKEAGVAFNTAPDESGRMTYRIDGSTTDDIGRLAFERGIALLELSETRASLEEAFLETTGEAVQYQAGSVDNND
>NZ_CP018175.1|WP_074492444.1|2920743_2921247_-|NUDIX-hydrolase
MDTMKGDGDGWAAAPNGGAVWGKNGAAGLLLVADKQMLMQHRAAWTNNGDTWALPGGARDSHETAAESALREAFEETGILPDDVEVLDSIVTAGPFPADPERPELAGNWTYTTVIARTKTGETLETTANEESLELRWVDIAAVDSLALMPAFAKAWPSLRKLLNTTE
>NZ_CP018175.1|WP_075348530.1|2921441_2922830_+|hypothetical-protein
MDTDDSSDHWLDPLTEKDTSKRTLVNSIVQETFGQPIFVARKIWAFVNTSPGRMTLMTIIISIAIFAAGYAMSVSSDTRQSNLDDLITNAEPVSYNAHVLYTSLAVADTTATTGFVQAGVEGPVNRVKYHTAIDRAAVAATHTAASADSSNEHLMELVLEIQRQLPVYTGLVETARTNNRAGNPVGVAYMSEASAMMRNEILPMASELYNLTSRAVSDQQRSVTGPQWFPLSGLLAALAMLVVAQWWLMRITRRRINKGFALATVMMMTATLWVSAANWATWQAGTKGFEEASGPLNSMTTARIYAQQTRTTETLSLVRRQSIQGSGTGFTATINQIKRALDEYETTAQSQTPEHQQLITAIRNAIAAWTADHDEFTVLLASGEYNGAVSAVLNKDEEGQTSFDELDTALAELIADSRSSMRSYIQSGLQATELVSVMVMLLSVVSVLALWVGIRPRLQEYL
>NZ_CP018175.1|WP_038586019.1|2922830_2923865_+|glutamate-ABC-transporter-substrate-binding-protein
MHAFRRPPPLTTRVGAALLAATLLASCTPTPVEPAETLTALDPDAGPPLPPDSSIEAPGEKEPIVEAIENWPGSLRPDDLTPEERVPGIVNRGRIIVGVDQSQNLLSFRDPVTGELRGFEVELAREISRDIFGDPNKVDFRFVGSSDRLRSLDQGDVDIVIRSVTITDERAKLVEFSTPYLRTQTRMLTMESSGITSIADLPGHTICVTDGSTSLQRARTIAPEASILKTRNWSDCLMALQQHQAQVILGDDVILSGIAAQDPYTEILDTSLDSHSYGVAAASTTAETDSSGLIRQVNYTIERIRTDRMWWTMFDDWFGPYLWSYGPPQLQYMPEEEGTENDEG

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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

449268 : 486969

Catovirus(20.0%)

transposase

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_065366598.1\|449268_450534_-\|transposase	IS256 family transposase	A0A220NQR7	Corynebacterium_phage	7.8e-234	97.6
WP_075348072.1\|451837_454489_+	hypothetical protein	NA	NA	NA	NA
WP_155761551.1\|454528_455395_+	hypothetical protein	NA	NA	NA	NA
WP_075348073.1\|455432_456809_+	glycosyltransferase family 25 protein	NA	NA	NA	NA
WP_060563805.1\|457027_457912_+	ABC transporter permease	NA	NA	NA	NA
WP_077311031.1\|458039_458762_+	ABC transporter ATP-binding protein	NA	NA	NA	NA
WP_075348074.1\|460705_461128_-	hypothetical protein	NA	NA	NA	NA
WP_089158484.1\|461515_466045_-	glycosyltransferase	A0A1V0SAE6	Catovirus	2.3e-33	31.6
WP_060563814.1\|466375_467629_-	UDP-N-acetyl-D-mannosamine dehydrogenase	M1HFY9	Paramecium_bursaria_Chlorella_virus	8.8e-20	25.0
WP_081302975.1\|470945_473138_-	hypothetical protein	NA	NA	NA	NA
WP_060563823.1\|473180_474089_-\|transposase	IS982 family transposase	NA	NA	NA	NA
WP_060563825.1\|474367_475555_+	hypothetical protein	NA	NA	NA	NA
WP_075348077.1\|475589_478817_+	glycosyltransferase	A0A1V0SAE6	Catovirus	6.8e-32	28.3
WP_081299819.1\|479075_479360_-\|transposase	transposase	NA	NA	NA	NA
WP_060563542.1\|479407_480718_-\|transposase	ISL3-like element IS13869 family transposase	A0A2H4PDF8	Mycobacterium_phage	2.5e-86	44.2
WP_089158485.1\|481227_481566_+\|transposase	transposase	NA	NA	NA	NA
WP_152024167.1\|481379_482162_+\|transposase	IS3 family transposase	Q6J1X2	Lactobacillus_phage	5.9e-14	28.6
WP_152024168.1\|482139_483341_-\|transposase	IS3 family transposase	Q6J1X2	Lactobacillus_phage	1.2e-26	30.5
WP_075348078.1\|483399_483579_-\|transposase	transposase	A0A1B3AZF8	Gordonia_phage	2.4e-08	49.1
WP_075348079.1\|483718_484054_+\|transposase	transposase	NA	NA	NA	NA
WP_075348475.1\|484489_485899_+	dihydrolipoyl dehydrogenase	A0A2K5B2C5	Erysipelothrix_phage	1.1e-45	29.2
WP_075348476.1\|486090_486969_+	UTP--glucose-1-phosphate uridylyltransferase	A0A127AW70	Bacillus_phage	9.4e-45	39.9

DBSCAN-SWA_2

1492302 : 1554787

Shigella_phage(18.18%)

transposase,integrase

attL 1545411:1545462|attR 1560331:1560382

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_081378006.1\|1492302_1493550_-\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_075348190.1\|1495659_1496895_+	restriction endonuclease subunit S	NA	NA	NA	NA
WP_065366844.1\|1496891_1499978_+	HsdR family type I site-specific deoxyribonuclease	A0A220A398	Liberibacter_phage	1.8e-58	29.3
WP_081299843.1\|1499961_1500708_+	M48 family metallopeptidase	NA	NA	NA	NA
WP_075348191.1\|1500749_1502381_+	AAA family ATPase	NA	NA	NA	NA
WP_060564452.1\|1502377_1503475_+	AAA family ATPase	NA	NA	NA	NA
WP_060564454.1\|1504369_1505335_-	hypothetical protein	NA	NA	NA	NA
WP_060564455.1\|1505335_1505617_-	hypothetical protein	NA	NA	NA	NA
WP_155762128.1\|1506485_1507325_+\|transposase	IS5 family transposase	NA	NA	NA	NA
WP_060564456.1\|1507405_1508329_+	hypothetical protein	NA	NA	NA	NA
WP_065366846.1\|1508462_1509875_+	hypothetical protein	NA	NA	NA	NA
WP_060564458.1\|1509969_1511196_+	leucine-rich repeat protein	NA	NA	NA	NA
WP_080506418.1\|1511861_1512119_-	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_060564459.1\|1512226_1513381_+	hypothetical protein	NA	NA	NA	NA
WP_011014272.1\|1513377_1513704_+	hypothetical protein	NA	NA	NA	NA
WP_065366847.1\|1513700_1515464_-	phosphomethylpyrimidine synthase ThiC	NA	NA	NA	NA
WP_107111918.1\|1515802_1516093_-	hypothetical protein	NA	NA	NA	NA
WP_060565493.1\|1516632_1516962_+	hypothetical protein	NA	NA	NA	NA
WP_034983522.1\|1517240_1518551_+\|transposase	ISL3-like element IS31831 family transposase	A0A2H4PDF8	Mycobacterium_phage	1.0e-82	42.2
WP_065366848.1\|1518636_1521024_-	glycogen/starch/alpha-glucan phosphorylase	Q8B3H5	Iris_mild_mosaic_virus	6.4e-19	47.7
WP_003861489.1\|1521219_1521378_-	hypothetical protein	A0A1V0SKJ6	Klosneuvirus	8.2e-08	60.0
WP_065366849.1\|1521435_1522845_-	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_075348192.1\|1522952_1523705_-	sulfite exporter TauE/SafE family protein	NA	NA	NA	NA
WP_060564463.1\|1523754_1524234_-	hypothetical protein	NA	NA	NA	NA
WP_060564464.1\|1524294_1524861_+	bifunctional (p)ppGpp synthetase/guanosine-3',5'-bis(diphosphate) 3'-pyrophosphohydrolase	A0A2I2L310	Orpheovirus	1.6e-08	36.8
WP_003861499.1\|1524843_1525551_-	IclR family transcriptional regulator	NA	NA	NA	NA
WP_060564465.1\|1525804_1527250_+	3-isopropylmalate dehydratase large subunit	NA	NA	NA	NA
WP_060564466.1\|1527268_1527862_+	3-isopropylmalate dehydratase small subunit	NA	NA	NA	NA
WP_075348193.1\|1528208_1529288_-	NUDIX hydrolase	NA	NA	NA	NA
WP_003858852.1\|1529296_1529455_+	hypothetical protein	NA	NA	NA	NA
WP_003858849.1\|1529496_1530495_+	NAD(P)-dependent glycerol-3-phosphate dehydrogenase	NA	NA	NA	NA
WP_060564468.1\|1530519_1531602_+	D-alanine--D-alanine ligase	NA	NA	NA	NA
WP_060564469.1\|1531658_1532639_-	DUF3515 domain-containing protein	NA	NA	NA	NA
WP_060564470.1\|1532706_1533696_+	thiamine-phosphate kinase	NA	NA	NA	NA
WP_060564471.1\|1533695_1534445_+	uracil-DNA glycosylase	S4VZ65	Pandoravirus	1.2e-29	35.7
WP_075348492.1\|1534576_1536160_+	DAK2 domain-containing protein	NA	NA	NA	NA
WP_065366851.1\|1536164_1538288_+	ATP-dependent DNA helicase RecG	NA	NA	NA	NA
WP_003858832.1\|1538307_1538523_+	acetyl-CoA carboxylase biotin carboxyl carrier protein subunit	NA	NA	NA	NA
WP_003858829.1\|1538522_1539107_+	16S rRNA (guanine(966)-N(2))-methyltransferase RsmD	NA	NA	NA	NA
WP_060564475.1\|1539110_1539593_+	pantetheine-phosphate adenylyltransferase	A0A1B1IVQ3	uncultured_Mediterranean_phage	1.9e-15	30.8
WP_065532560.1\|1540164_1540929_-	amino acid ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	1.2e-27	37.6
WP_060564477.1\|1540932_1541883_-	amino acid ABC transporter permease	NA	NA	NA	NA
WP_003858822.1\|1541925_1542930_-	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_060564478.1\|1543029_1543839_+	DUF1266 domain-containing protein	NA	NA	NA	NA
WP_003858816.1\|1543921_1544902_-	DUF368 domain-containing protein	NA	NA	NA	NA
1545411:1545462	attL	NA	NA	NA	NA
WP_011014293.1\|1545549_1546308_-\|integrase	site-specific integrase	G9FH48	Rhodococcus_phage	1.8e-15	32.1
WP_011014294.1\|1546293_1546704_+	hypothetical protein	NA	NA	NA	NA
WP_003861519.1\|1546700_1547447_+	hypothetical protein	NA	NA	NA	NA
WP_075348194.1\|1547639_1548074_+	metallopeptidase	NA	NA	NA	NA
WP_155762129.1\|1548752_1549954_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.5e-27	34.2
WP_003858803.1\|1550059_1550674_+	DUF4258 domain-containing protein	NA	NA	NA	NA
WP_003858801.1\|1550676_1550898_+	DUF2283 domain-containing protein	NA	NA	NA	NA
WP_038583885.1\|1551546_1551981_-	hypothetical protein	NA	NA	NA	NA
WP_003858799.1\|1551996_1552212_-	hypothetical protein	NA	NA	NA	NA
WP_003858795.1\|1552650_1553022_-	hypothetical protein	NA	NA	NA	NA
WP_011014297.1\|1553042_1553360_-	hypothetical protein	NA	NA	NA	NA
WP_107111897.1\|1553600_1554787_-\|transposase	IS3-like element IS1206 family transposase	U5P429	Shigella_phage	5.4e-27	33.7
1560331:1560382	attR	NA	NA	NA	NA

DBSCAN-SWA_3

1792672 : 1798083

Corynephage(33.33%)

integrase

attL 1786878:1786891|attR 1797541:1797554

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
1786878:1786891	attL	NA	NA	NA	NA
WP_081299849.1\|1792672_1792984_+	TM2 domain-containing protein	A0A1B0T6B3	Bacillus_phage	4.4e-05	42.7
WP_060564601.1\|1793022_1793613_+	hypothetical protein	A0A1P8D5Q9	Corynebacterium_phage	2.6e-22	53.3
WP_060564602.1\|1794345_1795104_+	hypothetical protein	NA	NA	NA	NA
WP_060564603.1\|1795208_1795541_+	hypothetical protein	Q9ZWV7	Corynephage	2.8e-18	45.0
WP_060564604.1\|1795571_1796114_+\|integrase	tyrosine-type recombinase/integrase	Q9ZWV7	Corynephage	2.7e-10	31.0
WP_060564605.1\|1796217_1796448_+\|integrase	tyrosine-type recombinase/integrase	A0A1L6BZH2	Pasteurella_phage	1.3e-06	43.1
WP_065532569.1\|1796451_1798083_-	ABC-F family ATP-binding cassette domain-containing protein	A0A1V0SKJ1	Klosneuvirus	1.3e-36	26.9
1797541:1797554	attR	NA	NA	NA	NA

DBSCAN-SWA_4

3185723 : 3243382

Streptococcus_phage(13.33%)

transposase,integrase

attL 3212855:3212875|attR 3255681:3255701

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_040968032.1\|3185723_3186014_+\|transposase	transposase	NA	NA	NA	NA
WP_075348427.1\|3186557_3186764_+	hypothetical protein	NA	NA	NA	NA
WP_075348428.1\|3187039_3188602_-	hypothetical protein	NA	NA	NA	NA
WP_003860174.1\|3189386_3190013_-	recombinase family protein	A0A286S1P7	Klebsiella_phage	1.9e-23	36.4
WP_011013963.1\|3190362_3190722_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_046552205.1\|3190721_3191318_+	cadmium transporter	NA	NA	NA	NA
WP_003859023.1\|3191576_3192998_-	mercury(II) reductase	A0A2K5B2C5	Erysipelothrix_phage	1.2e-44	30.0
WP_003859021.1\|3193096_3193486_+	heavy metal-responsive transcriptional regulator	NA	NA	NA	NA
WP_060565376.1\|3193976_3194687_-\|transposase	IS6-like element ISCef5 family transposase	A0A077SL39	Escherichia_phage	3.6e-79	59.8
WP_040968043.1\|3195099_3195342_-	DUF2892 domain-containing protein	NA	NA	NA	NA
WP_003862071.1\|3195578_3196880_-	APC family permease	NA	NA	NA	NA
WP_075348429.1\|3196945_3198427_-	multicopper oxidase family protein	NA	NA	NA	NA
WP_003862069.1\|3198423_3198690_-	hypothetical protein	NA	NA	NA	NA
WP_081302982.1\|3199359_3199908_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	Q8W6R2	Burkholderia_virus	9.7e-40	54.2
WP_075348430.1\|3199868_3200153_+	heavy-metal-associated domain-containing protein	NA	NA	NA	NA
WP_075348431.1\|3200238_3200979_+	Crp/Fnr family transcriptional regulator	NA	NA	NA	NA
WP_011015535.1\|3201134_3201371_+	heavy-metal-associated domain-containing protein	NA	NA	NA	NA
WP_011015536.1\|3201576_3201894_+	hypothetical protein	NA	NA	NA	NA
WP_075348432.1\|3202537_3204415_+	cadmium-translocating P-type ATPase	E4ZFI9	Streptococcus_phage	4.6e-105	37.2
WP_003861174.1\|3205622_3205997_-	thioredoxin	A0A1J0GW78	Streptomyces_phage	4.5e-12	38.7
WP_075348433.1\|3206182_3206389_+	heavy-metal-associated domain-containing protein	NA	NA	NA	NA
WP_011015541.1\|3206561_3207908_+	MFS transporter	NA	NA	NA	NA
WP_003861180.1\|3207867_3208050_-	hypothetical protein	NA	NA	NA	NA
WP_075348434.1\|3208060_3208663_-	PadR family transcriptional regulator	NA	NA	NA	NA
WP_060565382.1\|3208869_3210402_-	replicative DNA helicase	A0A1P8VVQ6	Streptococcus_phage	1.1e-88	42.3
WP_003855068.1\|3211009_3211462_-	50S ribosomal protein L9	NA	NA	NA	NA
WP_060565383.1\|3211518_3212196_-	single-stranded DNA-binding protein	A0A1P8D5R5	Corynebacterium_phage	2.9e-49	52.7
WP_003855074.1\|3212232_3212520_-	30S ribosomal protein S6	NA	NA	NA	NA
3212855:3212875	attL	NA	NA	NA	NA
WP_075348435.1\|3212879_3213071_-	hypothetical protein	NA	NA	NA	NA
WP_011015546.1\|3213067_3214528_-	DUF2029 domain-containing protein	NA	NA	NA	NA
WP_075348436.1\|3214573_3216736_-	penicillin-binding protein	NA	NA	NA	NA
WP_060565385.1\|3216827_3217220_-	hypothetical protein	NA	NA	NA	NA
WP_003855083.1\|3217411_3217885_+	MarR family transcriptional regulator	NA	NA	NA	NA
WP_011015549.1\|3217912_3218857_+	universal stress protein	NA	NA	NA	NA
WP_003861203.1\|3218888_3219386_+	hypothetical protein	NA	NA	NA	NA
WP_038586445.1\|3219453_3219777_-	antibiotic biosynthesis monooxygenase	NA	NA	NA	NA
WP_060565387.1\|3219797_3220736_-	rhodanese-related sulfurtransferase	NA	NA	NA	NA
WP_075348437.1\|3220783_3222049_-	FtsX-like permease family protein	NA	NA	NA	NA
WP_003855103.1\|3222045_3222738_-	ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	1.0e-38	43.1
WP_060565535.1\|3222741_3224580_-	HlyD family efflux transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_003855107.1\|3224946_3226038_+	inositol-3-phosphate synthase	A0A0H4IPK5	Stenotrophomonas_phage	8.6e-72	42.4
WP_075348539.1\|3226113_3226668_-	hypothetical protein	NA	NA	NA	NA
WP_060565390.1\|3226733_3228221_-	DUF1846 domain-containing protein	NA	NA	NA	NA
WP_006285365.1\|3228589_3229003_+	hypothetical protein	NA	NA	NA	NA
WP_006285366.1\|3229179_3230085_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	U5P429	Shigella_phage	3.4e-13	27.5
WP_081299886.1\|3230398_3231604_-\|transposase	IS30 family transposase	Q9MBM9	Staphylococcus_prophage	2.1e-31	32.7
WP_060565391.1\|3232112_3232610_-	DNA starvation/stationary phase protection protein Dps	NA	NA	NA	NA
WP_075348438.1\|3232755_3233571_+	Fpg/Nei family DNA glycosylase	NA	NA	NA	NA
WP_060565393.1\|3233807_3234959_+	RtcB family protein	A0A0M5M6X2	Mycobacterium_phage	1.4e-136	63.2
WP_003855120.1\|3234965_3235442_-	methylated-DNA--[protein]-cysteine S-methyltransferase	A0A0G2Y1B6	Acanthamoeba_polyphaga_mimivirus	5.0e-16	42.7
WP_075348439.1\|3235456_3236470_-	zinc-binding alcohol dehydrogenase family protein	NA	NA	NA	NA
WP_075348440.1\|3236627_3237551_+	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_011898098.1\|3237854_3239033_+	MFS transporter	NA	NA	NA	NA
WP_038586475.1\|3239308_3240487_+	NADP-dependent malic enzyme	NA	NA	NA	NA
WP_065532602.1\|3240617_3241991_+	hypothetical protein	NA	NA	NA	NA
WP_075348441.1\|3242071_3243382_+\|transposase	ISL3 family transposase	A0A2H4PDF8	Mycobacterium_phage	1.7e-82	42.2
3255681:3255701	attR	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_CP018175

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