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_CP024632	Acinetobacter junii strain lzh-X15 chromosome, complete genome	2 crisprs	cas3,DEDDh,csa3,WYL	1	6	2	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP024632_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024632_1

424822-425115

Unclear

Consensus_repeat	Method
TGGTGGTGAAGATCGTCCACGTCG	CRT

4 spacers

The CRISPR arrays of NZ_CP024632_1

>merge|NZ_CP024632|1|424822-425115|CRT
AGGCGGTGAAGATCGTCCACGTCGTAGCTTCGATGATAAACCACGTGGTGAACGTCCATCATTTGGTGGTGAAGATCGTCCACGTCGCGAATTCAATTCTGATCGTCCACGTCGTGAAGGTGGTTTTGAAGACCGTCCACGTCGTAACTTTGATGATAAACCACGTGGTGAACGTCCATCATTTGGTGGTGAAGATCGTCCACGTCGCGAATTCAATTCTGATCGTCCACGCCGCGAAGGTGGTTTTGATGATCGTCCAAAACGTACATTTGGTGGTGAAGATCGCCCACGTCG

>NZ_CP024632|1|1|424822-425115|CRT
AGGCGGTGAAGATCGTCCACGTCG	TAGCTTCGATGATAAACCACGTGGTGAACGTCCATCATT
TGGTGGTGAAGATCGTCCACGTCG	CGAATTCAATTCTGATCGTCCACGTCGTGAAGG
TGGTTTTGAAGACCGTCCACGTCG	TAACTTTGATGATAAACCACGTGGTGAACGTCCATCATT
TGGTGGTGAAGATCGTCCACGTCG	CGAATTCAATTCTGATCGTCCACGCCGCGAAGGTGGTTTTGATGATCGTCCAAAACGTACATT
TGGTGGTGAAGATCGCCCACGTCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024632.1\|WP_099948031.1\|420228_422124_+\|1-deoxy-D-xylulose-5-phosphate-synthase	unknown	unknown	gnl\|CDD\|235470
NZ_CP024632.1\|WP_099948034.1\|431388_431973_+\|TIGR00730-family-Rossman-fold-protein	unknown	unknown	gnl\|CDD\|129813
NZ_CP024632.1\|WP_004951721.1\|417041_417830_-\|shikimate-dehydrogenase	unknown	unknown	gnl\|CDD\|234703
NZ_CP024632.1\|WP_099948030.1\|414669_416991_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024632.1\|WP_099948028.1\|410097_411207_+\|HPP-family-protein	unknown	unknown	gnl\|CDD\|225979
NZ_CP024632.1\|WP_004951734.1\|422246_423077_+\|inositol-monophosphatase	unknown	unknown	gnl\|CDD\|238817
NZ_CP024632.1\|WP_099948035.1\|431982_432369_+\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|240046
NZ_CP024632.1\|WP_004909415.1\|430224_431238_-\|magnesium-and-cobalt-transport-protein-CorA	unknown	unknown	gnl\|CDD\|213369
NZ_CP024632.1\|WP_039047481.1\|425877_426696_+\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|213228
NZ_CP024632.1\|WP_004909424.1\|426692_427469_+\|lipid-asymmetry-maintenance-ABC-transporter-permease-subunit-MlaE	unknown	unknown	gnl\|CDD\|223838
NZ_CP024632.1\|WP_099948029.1\|412606_414430_-\|acyl-CoA-dehydrogenase-C-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|185635
NZ_CP024632.1\|WP_099948033.1\|429416_429866_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024632.1\|WP_153569569.1\|428210_428795_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|377516
NZ_CP024632.1\|WP_004964385.1\|428806_429094_+\|STAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|379202
NZ_CP024632.1\|WP_004760601.1\|411271_411541_-\|PspC-domain-containing-protein	unknown	unknown	gnl\|CDD\|377200
NZ_CP024632.1\|WP_004951723.1\|418246_419188_-\|oxygen-dependent-coproporphyrinogen-oxidase	unknown	unknown	gnl\|CDD\|235413
NZ_CP024632.1\|WP_099949461.1\|419319_419922_-\|GTP-cyclohydrolase-II	unknown	unknown	gnl\|CDD\|234745
NZ_CP024632.1\|WP_099948036.1\|432358_433018_-\|ComF-family-protein	unknown	unknown	gnl\|CDD\|223970
NZ_CP024632.1\|WP_004909422.1\|427468_428143_+\|outer-membrane-lipid-asymmetry-maintenance-protein-MlaD	unknown	unknown	gnl\|CDD\|275223
NZ_CP024632.1\|WP_099949460.1\|411884_412553_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP024632.1\|WP_099948031.1\|420228_422124_+\|1-deoxy-D-xylulose-5-phosphate-synthase	gnl\|CDD\|235470	PRK05444, PRK05444, 1-deoxy-D-xylulose-5-phosphate synthase; Provisional.	0
NZ_CP024632.1\|WP_099948034.1\|431388_431973_+\|TIGR00730-family-Rossman-fold-protein	gnl\|CDD\|129813	TIGR00730, LOG_family_protein_YJL055W, TIGR00730 family protein. This model represents one branch of a subfamily of proteins of unknown function. Both PSI-BLAST and weak hits by this model show a low level of similarity to and suggest an evolutionary relationship of the subfamily to the DprA/Smf family of DNA-processing proteins involved in chromosomal transformation with foreign DNA. Both Aquifex aeolicus and Mycobacterium leprae have one member in each of two branches of this subfamily, suggesting that the branches may have distinct functions. [Hypothetical proteins, Conserved].	3.64731e-64
NZ_CP024632.1\|WP_004951721.1\|417041_417830_-\|shikimate-dehydrogenase	gnl\|CDD\|234703	PRK00258, aroE, shikimate 5-dehydrogenase; Reviewed.	3.74584e-112
NZ_CP024632.1\|WP_153569569.1\|428210_428795_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|377516	pfam05494, MlaC, MlaC protein. MlaC is a component of the Mla pathway, an ABC transport system that functions to maintain the asymmetry of the outer membrane. This family of proteins is involved in toluene tolerance, which is mediated by increased cell membrane rigidity resulting from changes in fatty acid and phospholipid compositions, exclusion of toluene from the cell membrane, and removal of intracellular toluene by degradation. Many proteins are involved in these processes.	5.93844e-42
NZ_CP024632.1\|WP_099948028.1\|410097_411207_+\|HPP-family-protein	gnl\|CDD\|225979	COG3448, COG3448, CBS-domain-containing membrane protein [Signal transduction mechanisms].	1.59748e-99
NZ_CP024632.1\|WP_004951734.1\|422246_423077_+\|inositol-monophosphatase	gnl\|CDD\|238817	cd01639, IMPase, IMPase, inositol monophosphatase and related domains. A family of Mg++ dependent phosphatases, inhibited by lithium, many of which may act on inositol monophosphate substrate. They dephosphorylate inositol phosphate to generate inositol, which may be recycled into inositol lipids; in eukaryotes IMPase plays a vital role in intracellular signaling. IMPase is one of the proposed targets of Li+ therapy in manic-depressive illness. This family contains some bacterial members of the inositol monophosphatase family classified as SuhB-like. E. coli SuhB has been suggested to participate in posstranscriptional control of gene expression, and its inositol monophosphatase activity doesn't appear to be sufficient for its cellular function. It has been proposed, that SuhB plays a role in the biosynthesis of phosphatidylinositol in mycobacteria.	2.14602e-112
NZ_CP024632.1\|WP_099948035.1\|431982_432369_+\|NUDIX-domain-containing-protein	gnl\|CDD\|240046	cd04690, Nudix_Hydrolase_31, Members of the Nudix hydrolase superfamily catalyze 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 and contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which functions as a metal binding and catalytic site. Substrates of nudix hydrolases 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 & "house-cleaning" enzymes. Substrate specificity is used to define 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.	1.28245e-37
NZ_CP024632.1\|WP_004909415.1\|430224_431238_-\|magnesium-and-cobalt-transport-protein-CorA	gnl\|CDD\|213369	cd12835, EcCorA-like_1, Escherichia coli Mg2+ transporter CorA_like subgroup. A bacterial subgroup of the Escherichia coli CorA-Salmonella typhimurium ZntB_like (EcCorA_ZntB-like) family of the MIT superfamily of essential membrane proteins involved in transporting divalent cations (uptake or efflux) across membranes. This subgroup includes the Mg2+ transporters Escherichia coli CorA and Salmonella typhimurium CorA (which can also transport Co2+, and Ni2+). Structures of the intracellular domain of Vibrio parahaemolyticus and Salmonella typhimurium ZntB form funnel-shaped homopentamers, the tip of the funnel is formed from two C-terminal transmembrane (TM) helices from each monomer, and the large opening of the funnel from the N-terminal cytoplasmic domains. The GMN signature motif of the MIT superfamily occurs just after TM1, mutation within this motif is known to abolish Mg2+ transport through Salmonella typhimurium CorA, and Mrs2p. Natural variants such as GVN and GIN, such as occur in some ZntB family proteins, may be associated with the transport of different divalent cations, such as zinc and cadmium. The functional diversity of MIT transporters may also be due to minor structural differences regulating gating, substrate selection, and transport.	2.74778e-129
NZ_CP024632.1\|WP_004760601.1\|411271_411541_-\|PspC-domain-containing-protein	gnl\|CDD\|377200	pfam04024, PspC, PspC domain. This family includes Phage shock protein C (PspC) that is thought to be a transcriptional regulator. The presumed domain is 60 amino acid residues in length.	9.59509e-21
NZ_CP024632.1\|WP_039047481.1\|425877_426696_+\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|213228	cd03261, ABC_Org_Solvent_Resistant, ATP-binding cassette transport system involved in resistant to organic solvents. ABC transporters are a large family of proteins involved in the transport of a wide variety of different compounds, like sugars, ions, peptides, and more complex organic molecules. The nucleotide binding domain shows the highest similarity between all members of the family. ABC transporters are a subset of nucleotide hydrolases that contain a signature motif, Q-loop, and H-loop/switch region, in addition to, the Walker A motif/P-loop and Walker B motif commonly found in a number of ATP- and GTP-binding and hydrolyzing proteins.	1.02606e-139
NZ_CP024632.1\|WP_004909424.1\|426692_427469_+\|lipid-asymmetry-maintenance-ABC-transporter-permease-subunit-MlaE	gnl\|CDD\|223838	COG0767, Ttg2B, ABC-type transport system involved in resistance to organic solvents, permease component [Secondary metabolites biosynthesis, transport, and catabolism].	2.23346e-82
NZ_CP024632.1\|WP_099948029.1\|412606_414430_-\|acyl-CoA-dehydrogenase-C-terminal-domain-containing-protein	gnl\|CDD\|185635	PTZ00456, PTZ00456, acyl-CoA dehydrogenase; Provisional.	0
NZ_CP024632.1\|WP_099948036.1\|432358_433018_-\|ComF-family-protein	gnl\|CDD\|223970	COG1040, ComFC, Predicted amidophosphoribosyltransferases [General function prediction only].	4.85519e-31
NZ_CP024632.1\|WP_004909422.1\|427468_428143_+\|outer-membrane-lipid-asymmetry-maintenance-protein-MlaD	gnl\|CDD\|275223	TIGR04430, OM_asym_MlaD, outer membrane lipid asymmetry maintenance protein MlaD. Members of this protein family are the MlaD (maintenance of Lipid Asymmetry D) protein of an ABC transport system that seems to remove phospholipid from the outer leaflet of the Gram-negative bacterial outer membrane (OM), leaving only lipopolysaccharide in the outer leaflet. The Mla locus has long been associated with toluene tolerance, consistent with the proposed role in retrograde transport of phospholipid and therefore with maintaining the integrity of the OM as a protective barrier.	1.99373e-46
NZ_CP024632.1\|WP_004951723.1\|418246_419188_-\|oxygen-dependent-coproporphyrinogen-oxidase	gnl\|CDD\|235413	PRK05330, PRK05330, oxygen-dependent coproporphyrinogen oxidase.	0
NZ_CP024632.1\|WP_099949461.1\|419319_419922_-\|GTP-cyclohydrolase-II	gnl\|CDD\|234745	PRK00393, ribA, GTP cyclohydrolase II RibA.	3.06078e-125
NZ_CP024632.1\|WP_004964385.1\|428806_429094_+\|STAS-domain-containing-protein	gnl\|CDD\|379202	pfam13466, STAS_2, STAS domain. The STAS (after Sulphate Transporter and AntiSigma factor antagonist) domain is found in the C-terminal region of Sulphate transporters and bacterial antisigma factor antagonists. It has been suggested that this domain may have a general NTP binding function.	0.000182003

>NZ_CP024632.1|WP_004951734.1|422246_423077_+|inositol-monophosphatase
MEPMVVMAARAAQTVGQELLKAHQNRHKLDLQVEEKGIDGPVTRVDRYLEQLTIDTLRKSYKNHSFLGEEFGMQEGKGHDADWCWVIDPLDGTQNFINGFPHFCISIAVQHKGVTQHGVIYDPVRDELFSASRGRGAVMNQRRIRANVKDTLDKTFLAVGHPYRAKRNGEIVSYAEQHFASLLAVTKSGAQIRRAGSAALDLAYVAAGRFDGFFELGLKPWDIAAGELIVKEAGGVVVDARGGNDSMENGQVIACSMKMLKPLMQAVVPAWSEAAK
>NZ_CP024632.1|WP_099948031.1|420228_422124_+|1-deoxy-D-xylulose-5-phosphate-synthase
MLYTEIPTQRPVTPLLDEIDHPEQLRQLEQSQLPQVADELRQYILYAAGQSGGHFGANLGVIELTVALHYCFNTPDDRLVWDVGHQAYPHKVLTGRRERITTIRSKGGLAAFPARDESDFDTFGVGHSSTAISAGLGMALARRYQQKPCEVVAIIGDGAMTAGMAFEAMNDAVAHDADLIVVLNDNDMSISCSTGGFAKHLAAIWETGQLVNVNEQGEAYVQPHPKWTYNSRLHQSATDAADNLFKAIGFDYFGPFDGHNVEQLAQVFHALKKRKGPRLVHVYTKKGKGFAPAEADPITYHAITKITPTASAPVKKSPPKYSDVFGQWLCDEAEQDVRLLAITPAMCEGSGMVKFAQQYPERFFDVAIAEQHAVTLAAGMACEGLKPVVAIYSTFLQRGYDQLIHDVALQNLDVTFGIDRAGLVGEDGPTHAGAYDYAYMRTVPNMVIMAPKDENECRQMLHTAYHYKGPTAVRYPRGAGTGVEIQQQMTALEIGKAEIVAEFNLDADQQISILAFGSRVAASVEAAQQFANKHAIGVRVVNMRFVKPLDEQMIRTLAERTQLFVTVEEHAVMAGAGSAVNEFLAQAKIVKPILNLGLPDEFLHQATHQQMLTDCGLDAHGILASIERAWF
>NZ_CP024632.1|WP_099949461.1|419319_419922_-|GTP-cyclohydrolase-II
MPIEFIATSKLPTAFGDFNISVFQDPKTGEEHVALSKGLETPPNTPVLVRIHSECLTGDAFASLKCDCGPQLQATQRLINEAGQGVILYLRQEGRGIGLTNKIRAYALQDQGHDTVDANLLLNLPADARRYDMCSIMLDHLQVKKVKLITNNPLKLKALTDLGINVVERVPLTVGKNPFNEQYLKTKRERMDHLYQKDDF
>NZ_CP024632.1|WP_004951723.1|418246_419188_-|oxygen-dependent-coproporphyrinogen-oxidase
MQHPTSADIQRVREFLLDLQARICAGLEQQERAGGGTAEFIIDDWERTEGGGGRSRVLQNGEVIEKGGVMFSHINISKLPASATERHPQIAGAKAQALGVSLVIHPKNPNIPTSHANVRLFVAEPEGQDPVWWFGGGFDLTPFYPDDQDIQNWHQTAYDLCKPFGENVYAEHKQWCDDYFYLKHRDEQRGVGGLFFDDLNQWDFETCFKYMQAVGNGYLEAILPIFEKHREQPYTEAQREFQLYRRGRYVEYNLVYDRGTLFGLQTGGRIESILVSLPNLAGWSYRPEWDADSSEKRLTDYYLKPRDWLGLTK
>NZ_CP024632.1|WP_004951721.1|417041_417830_-|shikimate-dehydrogenase
MTKQFAVIGNPIEQSRSPELHHAFAAKTGVDLNYKKILAPLDGFESAVKAFFDQNGVGMNVTVPFKEQAFALCDQLTERAKIAKAVNTLWMQDGQLYGDNTDGQGLVAAIQALNWNLANSRILILGAGGATRGVIYPLVQAGAKQIVIANRTLARAEQLVEDLKTAVPDTELHAISLDQLTGEFDIVINATSASLTGEALQLPQTLIFHHAYEMAYGKPSSFLDQALIRQVPSTDGFGMLVGQAIEAFSIWNGVKPELKDFL
>NZ_CP024632.1|WP_099948030.1|414669_416991_+|hypothetical-protein
MRLKYLTLCLFGLSISGCSQHVIKTNSSSSSLEQKAINSINAMYEYPSYDYRGKFNIHVDLDQHKTEADQQKDVLDAALKQKVDQYLREQKVNLDAKQKQALYKALAEQPKGLGNSKFDKFARVMANILNDMQFEYDGSVHYRQKMGSFNLTARYEKPTLLVQAKVPMVLDLNNYKFYINYFALMPYLVNKENQNNLAYLDFSKYQGLFKQVDYKKFAEYIKASSAIYYRLADPNSIQALSVSSADQAAGVVEKIRLKTTIEELVLQANLYSKVNEKYLMQSILKFDEQNLEKLISEQDKTDTASKAEQSGTLLNSKAAADDASVVSQELYRLVNQHFGVEEPEDEYTDEADATKVAAEDVAQEAEDISEEADAVAESATATEQVLTGEQCTALQNAAKTNFGDIQYCQTMYDVDVLGEKKTPSGFLSYIEKLVAVEKEFVQYDQNQFIDDQGFKALWLKHQADIQKALPPFEKRNPFVMDVGLDAQGRAVKLDYDLNYALPELKSSFNIKADMLVTNYGKATPIDQAQLKQAKTWAEASKGSILEQAIGSFSEKLGQTGIQERSAQPYTLSLDDQLKVIAEQRYDATQSYEQTYKAVFIAKLVENNPSLAKRYTSQELQEVASVYAYWFSDEEVYSPEGKALKQIESLQKKHHLEQEDQFDDKLGQAVNRLVTDAMRGDQDRQQWKKLKAQYKQPQQLFAKQYQIQFEQTNGISNEEKSLLEQTANVLGQVYIDARKNQLSDKSLKALKIEHNEFIDYEIFKDVYQKMISTK
>NZ_CP024632.1|WP_099948029.1|412606_414430_-|acyl-CoA-dehydrogenase-C-terminal-domain-containing-protein
MPAYKAPLRDIRFLMNEVFDYPAHYQTLTSGQNADADTVDMILEGAADYCENVLSPINQSGDEEGCTFNNGEVTTPKGFKEAYDQFVMGGWQGLSYPEEFGGQGLPMSLNLIKSEMMGTANWSFTMYPGLSTGCMNTIMQFGTDEQKNTYMPKLVEGTWSGTMCLTEPQCGTDLGQVKTKAEAAADGTYKISGTKIFISAGEHDLTENIIHIVLARLPDSPAGTRGISLFIVPKFIPTADGGVGERNTVSCGSIEHKMGIRASATAVLNFDNATGYLIGEINKGLHAMFTFMNTARIGTAVQGIAHAELSFQGALPYAKDRMSMRALSGKKEPERVADAIIHHADVRRMLLTQKAVAEGGRAMIYHAAKLADKMTDALVNGDQAAYEAADDKLGFYTPILKGFLTELGLEAANHGIQVYGGHGFIKEWGMEQIARDARISTLYEGTTGIQALDLLGRKVLLSSKGKVVRDYTAEILKFCAAHARNKYLRRFAWDLTKLCAQWNTLTVRIMLAARKDRDIVSSASADFLMFSGYVMMAYFWAQQAVIASEKLEAGKGAETPEFYKAKIKVADFYFDRLLPRAQGHAESMVSTSRTLTSLAPEHFSFDY
>NZ_CP024632.1|WP_099949460.1|411884_412553_+|hypothetical-protein
MQFRLFLQPLSVGTLLVLGLTACDGHHPEPAISHSQTQPKPVGAAVSTALADDQAVTSEGVALTEVAGQATIPHVASKHMEKPSPKDLIYAGRYHARIPCSDPFAGCVNNENEAEYIINLLDDGSVFWTNTSFGRLGTDSSQNIAKIEQTCKQVHWHVHKDQNEIMIRCDAADVNLYYQINTNQDLVMNLDKIWNGDHGQNRKFFNEYPFPKKAYVFEKVKS
>NZ_CP024632.1|WP_004760601.1|411271_411541_-|PspC-domain-containing-protein
MANSGLYRSNQQSMIAGVMGGIAERFGWNANLLRLIFVIISIMSAAFPGILVYLIMWLVIPKRQANRVEHVQGYNQPVKTVYEDQGIKR
>NZ_CP024632.1|WP_099948028.1|410097_411207_+|HPP-family-protein
MNLTQLDWINLLKPNYKVLPVKERLFSGFGALCGLAISSLISWYVLGGMNVWYIAPMGASSVLLFAVPNSPLAQPWNVVVGNTLAGFIGVACTQLLPDLTTAFSVAVGLAIFMMMTTDSLHPPSGAVAITAVLGGEAVHKLGFHFILYPVLLNSLLLLVFAVFFNRLIGRNYPTMPHLNERSKDPTPTQKVSIQPKDIEYALEQHTELLDISQYDLEKIILEAQEHANERLNHSFVCQDIMSRDVIKLYENDDIHQALDKFKSVNLMSLPVVNDQDQLVGTLALYEVVEWFKGATDPRNSWQHYVKQIMSRRVVKVDPLQPIQDLVPYFVEKSFNYIPVVEELRLIGIISRADMIAALHQQIKQQSSIF
>NZ_CP024632.1|WP_039047481.1|425877_426696_+|ABC-transporter-ATP-binding-protein
MNNKTPRDTEALIEVKHLSFNRGERVIYDDVCLKIRRGQITAIMGPSGTGKTTLLRLIGGQLTPDRGEVLLDGKNIAAMSRSELFTARARMGMLFQSGALFTDMSVYENVAFPIRAHTKLPEHIIAELVALKLESVGLRGAEQLMPSELSGGMNRRVALARAIALDPELIMYDEPFAGQDPIVKGVLTRLIRSLREALDLTTIIVSHDVAETLSIADYIYVVAEGKIQGEGTPEQLENHASPFVRQFLTGSAEGPVEYQFTHQAYLDNEVRP
>NZ_CP024632.1|WP_004909424.1|426692_427469_+|lipid-asymmetry-maintenance-ABC-transporter-permease-subunit-MlaE
MNTIAWLGRLVIERVKGIGAASLMLIQILFSMPSKGGFQRFIYQMYRVGVMSLLIISVSGLFIGLVLGLQGYSILVNVGSEAMLGTMVSLTLLRELAPVVAALLFAGRAGSALTAEIGSMKQSEQLASMEMIGVDPLKQIVSPRLWAGIVSLPMLTVIFAAIGIVGGKLVGVDFLGVDEGSFWGGMQSSVQFGHDVVNGIIKSVVFALICTWVAVYQGYACDPTPEGIATSMTRTVVYSSLCVLGFDFVLTAVMFGGI
>NZ_CP024632.1|WP_004909422.1|427468_428143_+|outer-membrane-lipid-asymmetry-maintenance-protein-MlaD
MKSRTSELAVGIFVIIFGIALFFLAMKVSGLVGTNLRDSYSMTAQFDNVNGLKPRAKVTMSGVTIGRVESITLDPITRLATVKFELDGKLTSFNAEQLKEVQKNALEELRYSSDYQQADAAKQKEMEQQLIGNMTSITSLDEDAYIMVATNGLLGEKYLKVVPGGGVNYLKRGDVVSNTQGTMDLEDLISKFITGGAGKSTSSSSTESSASQPATDDAEPSFVE
>NZ_CP024632.1|WP_153569569.1|428210_428795_+|ABC-transporter-substrate-binding-protein
MLASAAFAAPKETPPDFVKRVADGLITRLKADKPKLQNNPALVRTIIRQNLDPYVDSQAFTRIVLGTYANNQYTNAAQRAQFEKNFREVIIENYGGAFAKYTNESYTMRPFKSTNSKNPVVTLDFMHNGEKIPVSFQLTDKGDQWKVRNINVSGIDLGLQFRNQFAATVQRNGGNIDKAIATFKPDADAAVNKK
>NZ_CP024632.1|WP_004964385.1|428806_429094_+|STAS-domain-containing-protein
MIQYIDQQLVVPKTIDFENAEQVYQSGLAYIQQHQSFPLVVDLAQLENGNTLSLAVLVQWLRQTPESKGLHFKNVSEKMLKIIQACHLQDDLKLI
>NZ_CP024632.1|WP_099948033.1|429416_429866_+|hypothetical-protein
MEIKSLFSRSIEFYVFAAVLIYAVVRLSISFINVNIMGDIIDENVRKNQFKQGYICFYDYKPQTGSKSKGSYGDREYFYYFYIDGKKSQNLIRPYFPFGEQWEGFIKRMDRRQCYQATYIEARFLFFTQRRIYQVFEKTVPSPYFKGEN
>NZ_CP024632.1|WP_004909415.1|430224_431238_-|magnesium-and-cobalt-transport-protein-CorA
MLEAFYATERGSLEDATINGSFDLHPELVWIDLIAPSQEEQQWVLDAYERNLPTLKSLEDISSSARFYRDDDGILHISTYFLTKNKNYQVDGDTDDSSHMLAMVQTVAFILHKDRLFTMRGEKLVAFRAFRARARRNDYDMDYKDPTWILLGLLEAKLDELADILEDIHKDLERYSTEVLNNHHREKILDLDDMITRLAQQEDMLGKAQLCLIDLRRVLTFLSRPRALGSHIYDADIRELSEDVRSLVEHDAFLFQKVRFLLDTTSGFINTEQNDTIRRFSILPSMLAPPMLIASIYGMNTDELPFAHGSLSFLVVAGILMAFLVLPMVYFRWKKWI
>NZ_CP024632.1|WP_099948034.1|431388_431973_+|TIGR00730-family-Rossman-fold-protein
MNSICVFCGSSLGNDVVYEKITQATGQIIAEQGLTLVYGGGRSGLMGVVANSALKAGGKVIGVIPEALVDRELAHAELSELYVVKDMHERKTKMAELADGFIALPGGAGTLEEIFEQWTWNQLGIHQKPCAFLNINGFYDDLIKMLQASVEHGFSQARFVDTLIVSDNIHDILTAFQKYQPAVPKWTSRNEIQA
>NZ_CP024632.1|WP_099948035.1|431982_432369_+|NUDIX-domain-containing-protein
MKTITVAAAVIMNDKNELLLVRKKNTRVFMQVGGKLEPNEAPEIAIQREILEEVGSTCDIKQYLGRYETATANEPDHQLISHLFVVELHQQPEIAAEIAEMKWIDLHEESILLAPLTTEVVIPWCLKQ
>NZ_CP024632.1|WP_099948036.1|432358_433018_-|ComF-family-protein
MFKLLSRGAQQVADYFTACHLCDIGVRAHHGVCQSCWQQLPWLKHKIERHQQDILIACHYEYPISQLIQQFKYEQQLHHLRLLSGLLLELKLPKVHAIVPMPISNDRLMERGFNQSLLIAKELSKVLNIPVWQPVQRLAQHSQKGLSRLERLENIEDQFVAKTHLQLIYRKVLIIDDVVTTGSSINALSQVLKQLGCQHIYSACLAAGGVKQANHDVIA

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Crispr_ID: NZ_CP024632_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024632_2

1451377-1452125

Orphan

I-F

Consensus_repeat	Method
TTTCTAAGCTACCTATGCGGTAGTAAAC	CRISPRCasFinder
TTTCTAAGCTACCTATGCGGTAGTAAAC	CRT
TTTCTAAGCTACCTATGCGGTAGTAAAC	PILER-CR

12 spacers

The CRISPR arrays of NZ_CP024632_2

>merge|NZ_CP024632|2|1451377-1452125|CRISPRCasFinder,CRT,PILER-CR
GTCATAAGCTACCTATGCGGTAGTGAACTTAAGCGCTGGACTGGACTTTTGATTGCACTTTTTCTAAGCTACCTATGCGGTAGTAAACTCCTCAGTATTTGATTGATACGTTAGGGATTTTTTCTAAGCTACCTATGCGGTAGTAAACTATCTGCACCAATCGTGCTACTTGCTATTGTTTTTCTAAGCTACCTATGCGGTAGTAAACTGGCTATTCAACTATGAAAAATGCTTTAACGTTTTCTAAGCTACCTATGCGGTAGTAAACCGTAGCTCGGTTAATCCCGTTTATTTCCCAATTTTCTAAGCTACCTATGCGGTAGTAAACACCCAACAGGGTACAAAACTTGATGTTTCACATTTCTAAGCTACCTATGCGGTAGTAAACTTAACTATTGCAGAACGTACAACACTTGCCACTTTTCTAAGCTACCTATGCGGTAGTAAACGATCGAATTTGGGATGAAGGTTTAGGTGTTTCTTTCTAAGCTACCTATGCGGTAGTAAACAGCCTGAGATACTTAACAAGCCTAGATAAGTATTTCTAAGCTACCTATGCGGTAGTAAACACGCTAAAACACAAACATCAGAACAAGCAACGTTTCTAAGCTACCTATGCGGTAGTAAACTTTTTCTTATAGAAAAACTTATAGCTATCTTGTTTCTAAGCTACCTATGCGGTAGTAAACATCATATTTTAATTTTCTCCGACCAATATCTATTTCTAAGCTACCTATGCGGTAGTAAAC

>NZ_CP024632|2|1|1451377-1452125|CRISPRCasFinder
GTCATAAGCTACCTATGCGGTAGTGAAC	TTAAGCGCTGGACTGGACTTTTGATTGCACTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TCCTCAGTATTTGATTGATACGTTAGGGATTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TATCTGCACCAATCGTGCTACTTGCTATTGTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TGGCTATTCAACTATGAAAAATGCTTTAACGT
TTTCTAAGCTACCTATGCGGTAGTAAAC	CGTAGCTCGGTTAATCCCGTTTATTTCCCAAT
TTTCTAAGCTACCTATGCGGTAGTAAAC	ACCCAACAGGGTACAAAACTTGATGTTTCACA
TTTCTAAGCTACCTATGCGGTAGTAAAC	TTAACTATTGCAGAACGTACAACACTTGCCACT
TTTCTAAGCTACCTATGCGGTAGTAAAC	GATCGAATTTGGGATGAAGGTTTAGGTGTTTC
TTTCTAAGCTACCTATGCGGTAGTAAAC	AGCCTGAGATACTTAACAAGCCTAGATAAGTA
TTTCTAAGCTACCTATGCGGTAGTAAAC	ACGCTAAAACACAAACATCAGAACAAGCAACG
TTTCTAAGCTACCTATGCGGTAGTAAAC	TTTTTCTTATAGAAAAACTTATAGCTATCTTG
TTTCTAAGCTACCTATGCGGTAGTAAAC	ATCATATTTTAATTTTCTCCGACCAATATCTA
TTTCTAAGCTACCTATGCGGTAGTAAAC

>NZ_CP024632|2|2|1451377-1452125|CRT
GTCATAAGCTACCTATGCGGTAGTGAAC	TTAAGCGCTGGACTGGACTTTTGATTGCACTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TCCTCAGTATTTGATTGATACGTTAGGGATTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TATCTGCACCAATCGTGCTACTTGCTATTGTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TGGCTATTCAACTATGAAAAATGCTTTAACGT
TTTCTAAGCTACCTATGCGGTAGTAAAC	CGTAGCTCGGTTAATCCCGTTTATTTCCCAAT
TTTCTAAGCTACCTATGCGGTAGTAAAC	ACCCAACAGGGTACAAAACTTGATGTTTCACA
TTTCTAAGCTACCTATGCGGTAGTAAAC	TTAACTATTGCAGAACGTACAACACTTGCCACT
TTTCTAAGCTACCTATGCGGTAGTAAAC	GATCGAATTTGGGATGAAGGTTTAGGTGTTTC
TTTCTAAGCTACCTATGCGGTAGTAAAC	AGCCTGAGATACTTAACAAGCCTAGATAAGTA
TTTCTAAGCTACCTATGCGGTAGTAAAC	ACGCTAAAACACAAACATCAGAACAAGCAACG
TTTCTAAGCTACCTATGCGGTAGTAAAC	TTTTTCTTATAGAAAAACTTATAGCTATCTTG
TTTCTAAGCTACCTATGCGGTAGTAAAC	ATCATATTTTAATTTTCTCCGACCAATATCTA
TTTCTAAGCTACCTATGCGGTAGTAAAC

>NZ_CP024632|2|1|1451437-1452125|PILER-CR
TTTCTAAGCTACCTATGCGGTAGTAAAC	TCCTCAGTATTTGATTGATACGTTAGGGATTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TATCTGCACCAATCGTGCTACTTGCTATTGTT
TTTCTAAGCTACCTATGCGGTAGTAAAC	TGGCTATTCAACTATGAAAAATGCTTTAACGT
TTTCTAAGCTACCTATGCGGTAGTAAAC	CGTAGCTCGGTTAATCCCGTTTATTTCCCAAT
TTTCTAAGCTACCTATGCGGTAGTAAAC	ACCCAACAGGGTACAAAACTTGATGTTTCACA
TTTCTAAGCTACCTATGCGGTAGTAAAC	TTAACTATTGCAGAACGTACAACACTTGCCACT
TTTCTAAGCTACCTATGCGGTAGTAAAC	GATCGAATTTGGGATGAAGGTTTAGGTGTTTC
TTTCTAAGCTACCTATGCGGTAGTAAAC	AGCCTGAGATACTTAACAAGCCTAGATAAGTA
TTTCTAAGCTACCTATGCGGTAGTAAAC	ACGCTAAAACACAAACATCAGAACAAGCAACG
TTTCTAAGCTACCTATGCGGTAGTAAAC	TTTTTCTTATAGAAAAACTTATAGCTATCTTG
TTTCTAAGCTACCTATGCGGTAGTAAAC	ATCATATTTTAATTTTCTCCGACCAATATCTA
TTTCTAAGCTACCTATGCGGTAGTAAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024632.1\|WP_099948546.1\|1455329_1455881_+\|DUF2799-domain-containing-protein	unknown	unknown	gnl\|CDD\|378521
NZ_CP024632.1\|WP_099948538.1\|1443575_1444637_-\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|378890
NZ_CP024632.1\|WP_099949492.1\|1449458_1450490_+\|lipase-secretion-chaperone	unknown	unknown	gnl\|CDD\|234937
NZ_CP024632.1\|WP_099948547.1\|1456021_1456480_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024632.1\|WP_153569912.1\|1452413_1453142_+\|ThiF-family-adenylyltransferase	unknown	unknown	gnl\|CDD\|238386
NZ_CP024632.1\|WP_099948545.1\|1454861_1455296_+\|2-amino-4-hydroxy-6--hydroxymethyldihydropteridine-diphosphokinase	unknown	unknown	gnl\|CDD\|376515
NZ_CP024632.1\|WP_099948548.1\|1456543_1457179_-\|2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinone-monooxygenase	unknown	unknown	gnl\|CDD\|153101
NZ_CP024632.1\|WP_099948544.1\|1453199_1454498_+\|AarF/ABC1/UbiB-kinase-family-protein	unknown	unknown	gnl\|CDD\|223733
NZ_CP024632.1\|WP_099948549.1\|1461428_1465934_+\|translocation/assembly-module-TamB-domain-containing-protein	unknown	unknown	gnl\|CDD\|225463
NZ_CP024632.1\|WP_099948541.1\|1447076_1448096_-\|AraC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|378890
NZ_CP024632.1\|WP_099948537.1\|1442115_1442934_+\|peptide-chain-release-factor-N(5)-glutamine-methyltransferase	unknown	unknown	gnl\|CDD\|236467
NZ_CP024632.1\|WP_099949493.1\|1458667_1461382_+\|BamA/TamA-family-outer-membrane-protein	unknown	unknown	gnl\|CDD\|223801
NZ_CP024632.1\|WP_004911755.1\|1454524_1454905_+\|dihydroneopterin-aldolase	unknown	unknown	gnl\|CDD\|224456
NZ_CP024632.1\|WP_099948543.1\|1450562_1451339_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP024632.1\|WP_099948539.1\|1445706_1446390_+\|superoxide-dismutase	unknown	unknown	gnl\|CDD\|223678
NZ_CP024632.1\|WP_004953941.1\|1457182_1458505_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|235865
NZ_CP024632.1\|WP_099949491.1\|1442930_1443563_-\|FMN-binding-negative-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225366
NZ_CP024632.1\|WP_099948540.1\|1446445_1447018_-\|flavin-reductase-family-protein	unknown	unknown	gnl\|CDD\|214900
NZ_CP024632.1\|WP_004953914.1\|1444779_1445550_+\|3-hydroxyacyl-CoA-dehydrogenase	unknown	unknown	gnl\|CDD\|187629
NZ_CP024632.1\|WP_099948542.1\|1448375_1449392_+\|triacylglycerol-lipase	unknown	unknown	gnl\|CDD\|224001

Protein	Function_ID	Function_description	E-value
NZ_CP024632.1\|WP_099948546.1\|1455329_1455881_+\|DUF2799-domain-containing-protein	gnl\|CDD\|378521	pfam10973, DUF2799, Protein of unknown function (DUF2799). Some members in this family of proteins are annotated as yfiL which has no known function.	1.64082e-21
NZ_CP024632.1\|WP_099948538.1\|1443575_1444637_-\|AraC-family-transcriptional-regulator	gnl\|CDD\|378890	pfam12625, Arabinose_bd, Arabinose-binding domain of AraC transcription regulator, N-term. AraC is a bacterial transcriptional regulatory protein with a DNA-binding domain at the C-terminus, HTH_AraC, pfam00165, and this dimerization domain which harbours the arabinose-binding pocket at the N-terminus. AraC positively and negatively regulates expression of the proteins required for the uptake and catabolism of the sugar L-arabinose 1,2,3].	5.7619e-32
NZ_CP024632.1\|WP_099949492.1\|1449458_1450490_+\|lipase-secretion-chaperone	gnl\|CDD\|234937	PRK01294, PRK01294, lipase secretion chaperone.	1.03699e-75
NZ_CP024632.1\|WP_153569912.1\|1452413_1453142_+\|ThiF-family-adenylyltransferase	gnl\|CDD\|238386	cd00757, ThiF_MoeB_HesA_family, ThiF_MoeB_HesA. Family of E1-like enzymes involved in molybdopterin and thiamine biosynthesis family. The common reaction mechanism catalyzed by MoeB and ThiF, like other E1 enzymes, begins with a nucleophilic attack of the C-terminal carboxylate of MoaD and ThiS, respectively, on the alpha-phosphate of an ATP molecule bound at the active site of the activating enzymes, leading to the formation of a high-energy acyladenylate intermediate and subsequently to the formation of a thiocarboxylate at the C termini of MoaD and ThiS. MoeB, as the MPT synthase (MoaE/MoaD complex) sulfurase, is involved in the biosynthesis of the molybdenum cofactor, a derivative of the tricyclic pterin, molybdopterin (MPT). ThiF catalyzes the adenylation of ThiS, as part of the biosynthesis pathway of thiamin pyrophosphate (vitamin B1). .	4.54677e-97
NZ_CP024632.1\|WP_099948545.1\|1454861_1455296_+\|2-amino-4-hydroxy-6--hydroxymethyldihydropteridine-diphosphokinase	gnl\|CDD\|376515	pfam01288, HPPK, 7,8-dihydro-6-hydroxymethylpterin-pyrophosphokinase (HPPK).	3.77088e-13
NZ_CP024632.1\|WP_099948548.1\|1456543_1457179_-\|2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinone-monooxygenase	gnl\|CDD\|153101	cd01042, DMQH, Demethoxyubiquinone hydroxylase, ferritin-like diiron-binding domain. Demethoxyubiquinone hydroxylases (DMQH) are members of the ferritin-like, diiron-carboxylate family which are present in eukaryotes (the CLK-1/CAT5 family) and prokaryotes (the Coq7 family). DMQH participates in one of the last steps of ubiquinone biosysnthesis and is responsible for DMQ hydroxylation, resulting in the formation of hydroxyubiquinone, a precursor of ubiquinone. CLK-1 is a mitochondrial inner membrane protein and Coq7 is a proposed interfacial integral membrane protein. Mutations in the Caenorhabditis elegans gene clk-1 affect biological timing and extend longevity. The conserved residues of a diiron center are present in this domain.	8.30313e-74
NZ_CP024632.1\|WP_099948544.1\|1453199_1454498_+\|AarF/ABC1/UbiB-kinase-family-protein	gnl\|CDD\|223733	COG0661, AarF, Predicted unusual protein kinase [General function prediction only].	3.46208e-92
NZ_CP024632.1\|WP_099948549.1\|1461428_1465934_+\|translocation/assembly-module-TamB-domain-containing-protein	gnl\|CDD\|225463	COG2911, COG2911, Uncharacterized protein conserved in bacteria [Function unknown].	8.87518e-108
NZ_CP024632.1\|WP_099948541.1\|1447076_1448096_-\|AraC-family-transcriptional-regulator	gnl\|CDD\|378890	pfam12625, Arabinose_bd, Arabinose-binding domain of AraC transcription regulator, N-term. AraC is a bacterial transcriptional regulatory protein with a DNA-binding domain at the C-terminus, HTH_AraC, pfam00165, and this dimerization domain which harbours the arabinose-binding pocket at the N-terminus. AraC positively and negatively regulates expression of the proteins required for the uptake and catabolism of the sugar L-arabinose 1,2,3].	1.04621e-15
NZ_CP024632.1\|WP_099948537.1\|1442115_1442934_+\|peptide-chain-release-factor-N(5)-glutamine-methyltransferase	gnl\|CDD\|236467	PRK09328, PRK09328, N5-glutamine S-adenosyl-L-methionine-dependent methyltransferase; Provisional.	1.00458e-120
NZ_CP024632.1\|WP_099949493.1\|1458667_1461382_+\|BamA/TamA-family-outer-membrane-protein	gnl\|CDD\|223801	COG0729, COG0729, Outer membrane protein [Cell envelope biogenesis, outer membrane].	4.4721e-61
NZ_CP024632.1\|WP_004911755.1\|1454524_1454905_+\|dihydroneopterin-aldolase	gnl\|CDD\|224456	COG1539, FolB, Dihydroneopterin aldolase [Coenzyme metabolism].	2.5342e-34
NZ_CP024632.1\|WP_099948543.1\|1450562_1451339_+\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	1.93943e-18
NZ_CP024632.1\|WP_099948539.1\|1445706_1446390_+\|superoxide-dismutase	gnl\|CDD\|223678	COG0605, SodA, Superoxide dismutase [Inorganic ion transport and metabolism].	3.92629e-101
NZ_CP024632.1\|WP_004953941.1\|1457182_1458505_-\|MFS-transporter	gnl\|CDD\|235865	PRK06814, PRK06814, acyl-[ACP]--phospholipid O-acyltransferase.	6.18328e-137
NZ_CP024632.1\|WP_099949491.1\|1442930_1443563_-\|FMN-binding-negative-transcriptional-regulator	gnl\|CDD\|225366	COG2808, PaiB, Transcriptional regulator [Transcription].	1.2874e-79
NZ_CP024632.1\|WP_099948540.1\|1446445_1447018_-\|flavin-reductase-family-protein	gnl\|CDD\|214900	smart00903, Flavin_Reduct, Flavin reductase like domain. This entry represents the FMN-binding domain found in NAD(P)H-flavin oxidoreductases (flavin reductases), a class of enzymes capable of producing reduced flavin for bacterial bioluminescence and other biological processes. This domain is also found in various other oxidoreductase and monooxygenase enzymes... This domain consists of a beta-barrel with Greek key topology, and is related to the ferredoxin reductase-like FAD-binding domain. The flavin reductases have a different dimerisation mode than that found in the PNP oxidase-like family, which also carries an FMN-binding domain with a similar topology.	2.29556e-24
NZ_CP024632.1\|WP_004953914.1\|1444779_1445550_+\|3-hydroxyacyl-CoA-dehydrogenase	gnl\|CDD\|187629	cd05371, HSD10-like_SDR_c, 17hydroxysteroid dehydrogenase type 10 (HSD10)-like, classical (c) SDRs. HSD10, also known as amyloid-peptide-binding alcohol dehydrogenase (ABAD), was previously identified as a L-3-hydroxyacyl-CoA dehydrogenase, HADH2. In fatty acid metabolism, HADH2 catalyzes the third step of beta-oxidation, the conversion of a hydroxyl to a keto group in the NAD-dependent oxidation of L-3-hydroxyacyl CoA. In addition to alcohol dehydrogenase and HADH2 activites, HSD10 has steroid dehydrogenase activity. Although the mechanism is unclear, HSD10 is implicated in the formation of amyloid beta-petide in the brain (which is linked to the development of Alzheimer's disease). Although HSD10 is normally concentrated in the mitochondria, in the presence of amyloid beta-peptide it translocates into the plasma membrane, where it's action may generate cytotoxic aldehydes and may lower estrogen levels through its use of 17-beta-estradiol as a substrate. HSD10 is a member of the SRD family, but differs from other SDRs by the presence of two insertions of unknown function. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold (alpha/beta folding pattern with a central beta-sheet), an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Classical SDRs are typically about 250 residues long, while extended SDRs are approximately 350 residues. Sequence identity between different SDR enzymes are typically in the 15-30% range, but the enzymes share the Rossmann fold NAD-binding motif and characteristic NAD-binding and catalytic sequence patterns. These enzymes catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase (15-PGDH) numbering). In addition to the Tyr and Lys, there is often an upstream Ser (Ser-138, 15-PGDH numbering) and/or an Asn (Asn-107, 15-PGDH numbering) contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Extended SDRs have additional elements in the C-terminal region, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif. Some atypical SDRs have lost catalytic activity and/or have an unusual NAD(P)-binding motif and missing or unusual active site residues. Reactions catalyzed within the SDR family include isomerization, decarboxylation, epimerization, C=N bond reduction, dehydratase activity, dehalogenation, Enoyl-CoA reduction, and carbonyl-alcohol oxidoreduction.	5.5005e-123
NZ_CP024632.1\|WP_099948542.1\|1448375_1449392_+\|triacylglycerol-lipase	gnl\|CDD\|224001	COG1075, LipA, Predicted acetyltransferases and hydrolases with the alpha/beta hydrolase fold [General function prediction only].	9.59094e-49

>NZ_CP024632.1|WP_099948543.1|1450562_1451339_+|alpha/beta-hydrolase
MWNRAEAGIGKPLVLLHGIGMSHKAWSPVIQQLSKSRRVIAFDVAGFGDSPSLGASVQPTIHNLVSALERELKTIGIHEPVDIVGNSMGGWMALEAARVGLASSVVAISPAGLWDESPAHVKMVFFSLRNAIKFMPNISRQMMGFALFRELLLAIPIGIGSRNISRKDALNSIDDFSKATDFDRTFANVGRFIGGKDIQVPLTIAFGTKDWLLRKKDCQNKSELPDHVNWLEPRDWGHVPMWKDPQGVADLILKNISD
>NZ_CP024632.1|WP_099949492.1|1449458_1450490_+|lipase-secretion-chaperone
MIGKRINSKLLIFSLISILLIVLGLIYWFFKPEEGLAQSRNSDSQSYNVTENDALAMSDSKNTTLPTLAPSLKGTEIDCPIQVDANGNLVLTVGIRSCFDYFFSSLGEKTETELIADIRQYLSATLPAPAAKYAAYLLEQYVGYMHTLQNAKPSGNFKTADVEELEKIINQMHKIQQQFFNAKEIEALFGNERNLNKFNIEQLRIHANKNLSTQQKAMELAKLIDQLPPTLADGVRVSMQFSELQQLTQEIKDKGGSPQELRSMRESLLGPEAADRLEKVDQEEAVWQSQVNNYLIKRDQILKSEMTDLNKQQAINQLRTSSFQSKEELLRAQSYEIMHDQKR
>NZ_CP024632.1|WP_099948542.1|1448375_1449392_+|triacylglycerol-lipase
MKKKYLSAMTLMAGMLISSGSVVHAGLFDFLAPKASWQNCDVNSCTVGGSTNVTSSYAKTKYPILLAHGMAGFSAVGPLQYWNGITEDLVGNGANVFVAQQASFNSSEVRGEQLLIQAKQVLAITGAQKINLIGHSHGTQSVRYVAGLLPNKIASVTAVGGPTKGSDVADVVYDFSKSPVGTIATPIIAAGVNAFFSLVGIGSGHYYEQDALAGMYSLTTRGAAEFNQRFPDGVPTTACGTGTELVNGVRYYSWSGTGVLTNVLDPFDYALAATSLLIPSENDGLVPRCSSHLGTVIRDNYAFNHLDEVNQVLGLVGFLQNPVTPYRIQANRLKNQGL
>NZ_CP024632.1|WP_099948541.1|1447076_1448096_-|AraC-family-transcriptional-regulator
MSIPRLYNHHFISSSYVHLLSEVVSHWNISAEELFWGTGVDVEQLNDFNHKISLSSFKKVIARSIELTQEEGIGFYAGTHLKISSHGLLGFTAAISKNAFEAIQTINQFVRIQCSFVELDFKIHDDLAYYTIVYEPSLLNFSDISDRQSYEFSCIFFLTGFVHLVRFFIPSFKPSLGLQCKYPAYFSRFKDILDSTFEVITFEESCTRLIASAKFLEMPLSLSDPLTSEKFKQLCQKELDELVATQDILYRVKQLIDDPIEGLLGIDQVAQKLNLTKRTLQRMLQEKSVSFQSLYDDVRKTKAQKLMLSPFASKDQIAKQLGYASTSSFNRAIKRWALE
>NZ_CP024632.1|WP_099948540.1|1446445_1447018_-|flavin-reductase-family-protein
MNQYIAPVELSKSYRLLNHGPTVLVSAQYNDEVNVMAAAWACALEFSPAKVTVVLDKTTKTRELVEKSGYFALQVPCYEQLNMVHQLGNISQFDDPEKLQTCKTEVFYQEDYSVPLVSGSIGWLICKLIPEPHNQQTHDLFIGSVIAAWADTRVFRDGHWHFSEEHKNLKSLHYIAGGTFYLIGEEVKAE
>NZ_CP024632.1|WP_099948539.1|1445706_1446390_+|superoxide-dismutase
MRMLNKSLFSLMLCAGLSVPAYAEFKQAPLPYKSDALEPAIDQKTMEIHYAKHHKAYVDNLNAQIKSYPELDKLSIEQVQAQISKYNSAVRNNGGGHFNHAFFWESLAPTNKTGKVSAKLLKQINQDFGSFEAFQDKFNQAATGRFGSGWAWLILNDAGQLEIVSTPNQDNPLMDIAEKKGQPLLGLDVWEHAYYLKYQNRRADYTKAFWSIVNWNTVNQRYDAAIK
>NZ_CP024632.1|WP_004953914.1|1444779_1445550_+|3-hydroxyacyl-CoA-dehydrogenase
MKIQGKHFVITGGGSGLGAATAEYLVQKGASVTLVDMNAEVGTQQAQALGEKAEFVQLDVTDEQAAEQFFKDVLVKHGAVHGLVNCAGIGPSAKVVGKDGVHDLGMFSKTLQINVTGTFNMLRLAAEAMSKNEVAEGDEDRGVIVNTASVAAFDGQIGQAAYSASKGAVVAMTLPIARELARHAIRIMVIAPGIMETPMLKGLPQNVQDALGQMVPYPSRLGRPEEFARLVAHIAENSYLNGEVIRLDGSIRMAAK
>NZ_CP024632.1|WP_099948538.1|1443575_1444637_-|AraC-family-transcriptional-regulator
MSKLPNQDINSAKDTISNALIREALSVAASRGLNIVNIANKAGISAELLTSTKARVPVNQSAQLWVELAKSMNDEFLGMDTHPMRRGSYKVLAKLAFGADTLEQAIQDILKFLALILDDIHGELVHEGSKAFLILHDRDQPKRMFTYSTFLMLVHSLMCWLSDQRISFHRMSFRCHQPVEIQDYRVRFCENIEFNAEHNKIEFDAHYLKHKIKKDKQALNEFLKHAPYNLIVRFKNENSLSLQIRRQLILQPPSEWAELKDIAQQMNMSTATIQRRLKQEGVSYQQLKNDIRCDIAIERLSKTNDSIQSISDDLNFHDPSAFHRAFKKWSGVSPGSYRKTSPSKKLLVNQFED
>NZ_CP024632.1|WP_099949491.1|1442930_1443563_-|FMN-binding-negative-transcriptional-regulator
MYLPEIFEEKNTEKLYQLVEKYPLGTLVTHSTNGIEANHLPFKLLHEPKSNHAILIAHIARSNELHTLIESGTDVLVIFQGEQGYISPNWYPSKQLHHRHVPTWNYQVVHVKGKIKFLEDEKSLRGILAKLTRTHEAKQEKPWKMSDAPSDYIAAELKQIIGIEIEIQHMTGKFKLSQNRDQSDAVNVVNNLEKQGQIQLAKAVKQYIED
>NZ_CP024632.1|WP_099948537.1|1442115_1442934_+|peptide-chain-release-factor-N(5)-glutamine-methyltransferase
MNIAQALEIKGEIDSYERQEAAWLLEHILGINSLELKLRLEQELTEIQEQAYLNGLARIDHGEPLAYVTGSQPFWTLDLKVTHDTLVPRPDTEILIETVLKLELDSTSNVVDLGTGTGAIALALASERPQWKVTATDIYQPTLEVAQENAIRHGLTHVKFACGAWFDALEKQFFDLIVSNPPYIDPEDVHMQMLKSEPERALIADKQGLADLETIIVQGRGWLNPNGWIVLEHGYDQGEAVRTIFEKEGFSQIQTIKDYGGNDRVSLGQKLN
>NZ_CP024632.1|WP_153569912.1|1452413_1453142_+|ThiF-family-adenylyltransferase
MHLYSRQILLDGWDIEAQEKLKLANVLIIGAGGIGCTSAELLARAGVGKITIVDADTIEMSNLQRQIAFTPNDIGRYKAEILAKHLQVINPHIHVSYKNIRFDETNADDLIQHQDVVLDGCDNFTTRYLANAICKKYQVPLISASAIGFEGQMFMVESDSACYECLFPKEDHANEGMRCAESGVLATTPVMIASLQAHHTLLFLGLGLTPLKQKLLLWNGLNLSQRILKFEKDANCPVCRAT
>NZ_CP024632.1|WP_099948544.1|1453199_1454498_+|AarF/ABC1/UbiB-kinase-family-protein
MKRNILFDGLRSVARIGETVIVAAQAGVKYATEKPSNAKLMRETFESLGSTYIKLGQFIASTPSLFPREYVEEFQGCLDQTPTLPFSYIQEVLAEEFEGKNLNEIFSFIDEKPLASASIAQVHAAKLVTGEDVVLKVQKPGVETILYTDLNVVHWATKLLERAVPKIKFASLSEIVDEIKTRMVREVDFIEEAQNLDDFVQYLNVSGNQAATAPKVYHQFSTRRVLTMQRLYGVSLTDFDVVKKYAKDPTQVLITAMNTWFGSLMLCKSFHADLHAGNLMLLEDGRVGFIDFGIVGQLKPEVWTACMAFMDALQHTNYAAMAENMLKMGMTHQKIDTQVLADDLERLFSGVLLADPQEILSSNPADLNDIMMDMIGVGERHGIKFPRDFALLFKQMLYFDRFMRVLAPYTDIYADQRLKMVHNIEPASFLKH
>NZ_CP024632.1|WP_004911755.1|1454524_1454905_+|dihydroneopterin-aldolase
MDAIIIEGLKVDTVIGCFNWERQIIQPLMLDLTIHNDLNQAAQSDELDDTLNYAQICELAAQVIQQAKPKLIEHAAQLVLEKLFLVFPSIESIIITIRKPAIIAQANAVGIRLERNRNDFCARTGE
>NZ_CP024632.1|WP_099948545.1|1454861_1455296_+|2-amino-4-hydroxy-6--hydroxymethyldihydropteridine-diphosphokinase
MNATETIFALALASNVQQQQNFTFAYAQLAQLGKVEFSAIYQIPCRDAVGADYWNSACLLKSELTVDEVLDILKNLETQSGRVRPSHYISLDIDVIAWGKDLEHMQFNPKKLPLANDVKIPLLELWQHEVLNYDDKLQYPVIKI
>NZ_CP024632.1|WP_099948546.1|1455329_1455881_+|DUF2799-domain-containing-protein
MKVIFLLTTLSFLLSGCAAMSVEQCKTANWFNVGEKDGSAGRESRLDQYYSSCQKANITPNQNLYEKGYQKGLNFYCRPETIFDEALEGRGDYRVCPIEKRDSLRAYYQVAHEYYQANSEFERSQTDISYYLKELERKDLSVKDRDDYKKRLYDLRLNSSRVQYRYQDAVRNLERFKAERGLQ
>NZ_CP024632.1|WP_099948547.1|1456021_1456480_+|hypothetical-protein
MRNILLVFSILQSILITNQAFAIDEKYRHQLEQSGCTQLSELQGCDIRKSKQENIKAGFLENNTQDALDGKSSSEPQWIAERTDGKILARIKIDDKERVWVNDYRVIAIKKKGQITFRLGKINYTIFTDQEKGSESFWYDRYSKDRGKIVLQ
>NZ_CP024632.1|WP_099948548.1|1456543_1457179_-|2-polyprenyl-3-methyl-6-methoxy-1,4-benzoquinone-monooxygenase
MRHYTGLDKMINSFDQALRSLVPGATTSQRNNPAEETPSQLCVSDARHVAGLMRVNHSGEVCAQALYHGQALTAKLPHVKQEMQQAALEEQDHLAWCEDRLKELDSHTSILNPIWYGLSYGMGAIAGIAGDKYSLGFVAETERQVSQHLQEHIQQLPTHDERSRKILEQMNEDELHHRETALNAGGVELPVPVKITMTAISKLMTKTSYYL
>NZ_CP024632.1|WP_004953941.1|1457182_1458505_-|MFS-transporter
MMKQDDHLMTSRRFVPMFFTQFFGALNDNVYKQALLLVITYGWIQQQSAPISTLNNLAALLFILPYFFFSATAGQIADKYERSQLIRFIKILEIVIMLIGTAGFLLGNLWLLLFALFLMGTHSTCFGPIKYAILPEILKPNELMSGNALFQSGTSIAILLGMILGGAVIASSEGNLLWISVTVVTIACLGYLSSRFILPQKIASPDLKIDWNFIRTSFQTLSYVKKIPVVFMILLGNSWYWFYGATYLTQIPQLTQQNLHASENVVSLLLTFFSVGIGVGSLLCRKIGGSDINIKMVPYGAIGLTVFALYLAASLAFVPERTGELLNLKDMFTQGLVYYHVMIAVTLLGISGGFYIVPLYAMMQAYSPRSHRARVVAANNILNAVFMVSSAIFSILILSILKIDIKILFIITAVLSAFFSIWLLKRLQPLLANAPHTLED
>NZ_CP024632.1|WP_099949493.1|1458667_1461382_+|BamA/TamA-family-outer-membrane-protein
MPSKDKFKQSTLVHSMHLIFKMQGFPKLICSSFIISSFISVACAQEQIADMSKINSIETPSSSDQTLQTLASADVNVSATVEPSTVTVSELDSLAALKQQEQTINQVEELKPIQFDENLEDLPVVSVDQNMANEIYRVAEEAKNEAKNYRANATQTTVNDVSQAELTEITKAPVNINQLMQEIQADSKIVVEANETGRTLADFLARSEPAPEKVGFFKKIINRFKPENILNTDKVPRISADVSGAPPELAANIKAKLSSFTQESFDDFAVALPQLRALSNQAAQAVGYYNAEFKFEKVSENKVKVNVTPNEPVIINEQNIDFTGAGENLPQFQVIRLVPIQDEKDIFNHGKYEETKSKIVNTATDNGFFDAYWRLHDVKISQPEKIADINLKYETGERYKLKKVEYRMSDPSKPLPLTQKVLDSLAPWKEGDDYAFWRVNLLANNLTNTRYFNYTLVDTIKPDPIQPPLELPPDLQALVDQQRIQESQLLNSQQKADLARQKVTSSQEVTQDVVDESQFSGGQAAQPYALARAMPLAHDHDDEEEERQKLEEQTRIEKKIPVVVTLNADRLNSLETGIGYGTDTGARIRSQYRRAIVNKYGHAFDANIELSQIRQSIDGRYSIPYKHPLNDYFNLVGGYEREERDDIGPDVNLLVESAVLGGERIIKNPLGDWQHTMGFRYRLDRLTKKGDVNVDELPDAFKVSGIDSEQESLLFGYEASKTNANSRLNPTKGFKQTYKVELGSESLLSDANMAILTAGWRFIYSLGENEDHQFVGRGDASYIFTDDFNKVPYNLRFFTGGDQSLRGFDYKSLSPEEDGYKIGGQALGVGSFEYNYQFKDGWRAAVFSDFGNAYDKQFSNPTEYSIGVGIRWRSPIGPIRLDVASGISNDNNPIRLHFFIGPQL
>NZ_CP024632.1|WP_099948549.1|1461428_1465934_+|translocation/assembly-module-TamB-domain-containing-protein
MSEVEQQLTPSNGPKKQRHTIRTIVLVLLMTLVVLISSLLVMMSTDKGSRFLLDRVLQSQKMIRYEYESGNLLSGIILKNVLVQLKAVDVSLDRADVSLGWRAVFKKEIHLSHADVQNLKVINKKPPSGKPFAFDAIKLPFVLRVDEANLDHLVIKTTTSEVKFNDIYLKDALWSGTKLEFEDSHMDMGYLAVKNATGQMDFSGKYPIDAKADLIIPSLKSLDINVIKVVASGTLDTLKAGVATQTPDLLTGWTVLHPVRDGVPMQGELLFKNYHLPLLKEQKLFAKNGVARFNGNTKKLILSLDTDLKGEQIPEGKYNALMETDLRNQLNIQDFNGQVMNGSVSLKGIVSWKDHVAWDIKGRLDRLNPKNKIIPQVAQDFLPPTLDANLSSIGSMEKGLALNAQLAFDKYETWNVKLNQAKAISNKPQPMLLDIAWQGIDRAVPYIGWLSSDNGQTNITLKEGQQDIFVSTTVKPHEKTVLPTGKYDARLDVKGSLLDIENFRYQAENGSLSGLAKIKLPTEKQQLSWSATLKADNFNPQTVATAAPVNLLNGQIVAKGFAKPNQQIIQFDNIDLNGQLAQSNTSEKIALKGKSTAALIFHDQKNGGGFKSYAVQYDGSLNALNQANGLLKIDVAGTPDYVKINELKHDGVAGKLFATGSVNLKDKLGWNIETSLVRFKPQYFVSSVKGEISGHVKSQGVWSDDLKRVDIRQLNAAGFINNKPVRGRGNLTLLLDSNQKGFLPQQFEANDLFFAYAQNQLQATGNAQSLKVKLNAPALYEIYPGLQGRAYGNLNIQSQPKLKATANIAVDNFAFNNLVSIKSLRVQGELPTSETTPTILTAKVNQVRNGNREIENAVVNLAGTRKAHLLKVESKNKQSNFYVQLAGGFNQNNDWLGQLQKGNFTSRRISLVQNQSAPIIYTSSAAELFVGQHCWSSSHSQLCLDQAARISKTKGNVSFLTKNLDLNDFAAFMPEGLAVTGQLNGYARASWANGTRPKLDATLVTRKGEIGLAAADPQDPATTVTYDELSLIAKSVGEGLLFRVDMKTPDIGTGYANVIINPFQSNMPMRGEIAFDEVQLKVFKPFIKDVRSMAGTLSLAGKVDGTLTQPQFTGEMRLKNGAISMISLPVNLNNIQLYSSIRQDSASIDGAFNSGQGVGRLKGSFDWKNDPHLALTLKGDNLLVRQAPMITAIVKPDLSLDVYPFAQRLSLKGTIDVPRARISMPESSATVVNVSPDVRVVHQGQDLLATLKAAKPWDIRADMTVNLGNQVIFQGFESNIPLVGRLHLSQRGLETAMRANGAIGVSQKVKIEAYGQSLDLNRAIARFNGPLANPTLDIDANKPVQGSMVGVRVTGTATVPNVQVYNDAGLSEQEALNALLTGRINEGGSGLSNTEGFKSDVNNTIAAAGISMGLGGTRALTNQIGRTFGLSGLALDAQGTGDDTQVSLTGYITPDLFIRYGIGVFTPVNKLTLRYQMNRRLYLEASQSLERAIDLFYNWRF

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP024632_1	1.2\|424909\|33\|NZ_CP024632\|CRT	424909-424941	33	NZ_CP024632.1	425116-425148	2	0.939

1. spacer 1.2|424909|33|NZ_CP024632|CRT matches to position: 425116-425148, mismatch: 2, identity: 0.939

cgaattcaattctgatcgtccacgtcgtgaagg	CRISPR spacer
cgagttcaattctgatcgcccacgtcgtgaagg	Protospacer
***.**************.**************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	MH617060	Inoviridae sp. isolate ctcg21, complete genome	4587-4618	2	0.938
NZ_CP024632_2	2.10\|1451946\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451946-1451977	32	KT894027	Dishui lake virophage 1, complete genome	9688-9719	7	0.781
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	CP020760	Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-21, complete sequence	6476-6507	7	0.781
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NC_005567	Bacillus thuringiensis H1.1 plasmid pGI3, complete sequence	4415-4446	7	0.781
NZ_CP024632_1	1.2\|424909\|33\|NZ_CP024632\|CRT	424909-424941	33	NZ_CP030363	Salinibacter ruber strain SP73 plasmid pSR118, complete sequence	70669-70701	8	0.758
NZ_CP024632_2	2.4\|1451585\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451585-1451616	32	NZ_CP043858	Arcobacter cibarius strain H743 plasmid pACIB, complete sequence	129065-129096	8	0.75
NZ_CP024632_2	2.4\|1451585\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451585-1451616	32	CP013001	Bacillus thuringiensis strain XL6 plasmid, complete sequence	113457-113488	8	0.75
NZ_CP024632_2	2.6\|1451705\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451705-1451736	32	AP018319	Nostoc sp. HK-01 plasmid plasmid1 DNA, complete genome	52021-52052	8	0.75
NZ_CP024632_2	2.8\|1451826\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451826-1451857	32	NZ_CP013139	Pseudoalteromonas sp. Bsw20308 plasmid pPBSW1, complete sequence	425082-425113	8	0.75
NZ_CP024632_2	2.10\|1451946\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451946-1451977	32	GU071103	Prochlorococcus phage P-SSM7, complete genome	83379-83410	8	0.75
NZ_CP024632_2	2.10\|1451946\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451946-1451977	32	MG250483	Aeromonas phage Ah1, complete genome	55593-55624	8	0.75
NZ_CP024632_2	2.10\|1451946\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1451946-1451977	32	NC_023688	Aeromonas phage PX29, complete genome	56683-56714	9	0.719
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NZ_CP004876	Bacillus thuringiensis serovar kurstaki str. HD-1 plasmid pBMB299, complete sequence	141399-141430	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NC_017203	Bacillus thuringiensis serovar chinensis CT-43 plasmid pCT281, complete sequence	173565-173596	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NC_020384	Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-285, complete sequence	177790-177821	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NZ_CP011350	Bacillus thuringiensis strain YC-10 plasmid pYC1, complete sequence	706998-707029	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NZ_CP015152	Bacillus thuringiensis strain Bc601 plasmid pBTBC2, complete sequence	4871-4902	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NZ_CP013056	Bacillus thuringiensis strain YWC2-8 plasmid pYWC2-8-1, complete sequence	26536-26567	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NZ_CP004861	Bacillus thuringiensis serovar kurstaki str. YBT-1520 plasmid pBMB293, complete sequence	138730-138761	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NZ_AP014866	Bacillus thuringiensis serovar tolworthi strain Pasteur Institute Standard strain plasmid pKK2, complete sequence	8828-8859	10	0.688
NZ_CP024632_2	2.11\|1452006\|32\|NZ_CP024632\|CRISPRCasFinder,CRT,PILER-CR	1452006-1452037	32	NZ_CP010091	Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence	133462-133493	10	0.688

1. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to MH617060 (Inoviridae sp. isolate ctcg21, complete genome) position: , mismatch: 2, identity: 0.938

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttatagaaaaatttataactatcttg	Protospacer
*****************.*****.********

2. spacer 2.10|1451946|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to KT894027 (Dishui lake virophage 1, complete genome) position: , mismatch: 7, identity: 0.781

acgctaaaacacaaacatcagaacaagcaacg	CRISPR spacer
attataaaacacaaacatcatcacaagcaccc	Protospacer
*.  ****************  ******* *

3. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to CP020760 (Bacillus thuringiensis strain ATCC 10792 plasmid pLDW-21, complete sequence) position: , mismatch: 7, identity: 0.781

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tctttcttatagaaacacctatagcaactttt	Protospacer
*.************* **.****** *..**

4. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NC_005567 (Bacillus thuringiensis H1.1 plasmid pGI3, complete sequence) position: , mismatch: 7, identity: 0.781

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tctttcttatagaaacacctatagcaactttt	Protospacer
*.************* **.****** *..**

5. spacer 1.2|424909|33|NZ_CP024632|CRT matches to NZ_CP030363 (Salinibacter ruber strain SP73 plasmid pSR118, complete sequence) position: , mismatch: 8, identity: 0.758

cgaattcaattctgatcgtccacg------tcgtgaagg	CRISPR spacer
cgaattccattctgatcgaccacggccatctcg------	Protospacer
******* ********** *****      ***

6. spacer 2.4|1451585|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP043858 (Arcobacter cibarius strain H743 plasmid pACIB, complete sequence) position: , mismatch: 8, identity: 0.75

tggctattcaactatgaaaaatgctttaacgt	CRISPR spacer
ttgcaattcaactatgaaagatgcttataaaa	Protospacer
* ** **************.******  * .

7. spacer 2.4|1451585|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to CP013001 (Bacillus thuringiensis strain XL6 plasmid, complete sequence) position: , mismatch: 8, identity: 0.75

tggctattcaactatgaaaaatgctttaacgt	CRISPR spacer
attctagtcaactatgtaaaatgctttttagt	Protospacer
   *** ********* **********   **

8. spacer 2.6|1451705|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to AP018319 (Nostoc sp. HK-01 plasmid plasmid1 DNA, complete genome) position: , mismatch: 8, identity: 0.75

acccaacagggtacaaaacttgatgtttcaca	CRISPR spacer
acccaacagggtacaaagctagagatgacgaa	Protospacer
*****************.** ** .*  *. *

9. spacer 2.8|1451826|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013139 (Pseudoalteromonas sp. Bsw20308 plasmid pPBSW1, complete sequence) position: , mismatch: 8, identity: 0.75

gatcgaatttgggatgaaggtttaggtgtttc	CRISPR spacer
aataaacaatgggataaaggtttaggtgattc	Protospacer
.** .*   ******.************ ***

10. spacer 2.10|1451946|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to GU071103 (Prochlorococcus phage P-SSM7, complete genome) position: , mismatch: 8, identity: 0.75

acgctaaaacacaaacatcagaacaagcaacg	CRISPR spacer
atactaaaacacaaacctcagatcaaggtaat	Protospacer
*..************* ***** ****  *

11. spacer 2.10|1451946|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to MG250483 (Aeromonas phage Ah1, complete genome) position: , mismatch: 8, identity: 0.75

acgctaaaacacaaacatcagaacaagcaacg	CRISPR spacer
actgatttacacatacaccagaacaagcaacg	Protospacer
**      ***** ***.**************

12. spacer 2.10|1451946|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NC_023688 (Aeromonas phage PX29, complete genome) position: , mismatch: 9, identity: 0.719

acgctaaaacacaaacatcagaacaagcaacg	CRISPR spacer
actgattgacaccaacaccagaacaagcaacc	Protospacer
**     .**** ****.*************

13. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP004876 (Bacillus thuringiensis serovar kurstaki str. HD-1 plasmid pBMB299, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

14. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NC_017203 (Bacillus thuringiensis serovar chinensis CT-43 plasmid pCT281, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

15. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NC_020384 (Bacillus thuringiensis serovar thuringiensis str. IS5056 plasmid pIS56-285, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

16. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP011350 (Bacillus thuringiensis strain YC-10 plasmid pYC1, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

17. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015152 (Bacillus thuringiensis strain Bc601 plasmid pBTBC2, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

18. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013056 (Bacillus thuringiensis strain YWC2-8 plasmid pYWC2-8-1, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

19. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP004861 (Bacillus thuringiensis serovar kurstaki str. YBT-1520 plasmid pBMB293, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

20. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_AP014866 (Bacillus thuringiensis serovar tolworthi strain Pasteur Institute Standard strain plasmid pKK2, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

21. spacer 2.11|1452006|32|NZ_CP024632|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP010091 (Bacillus thuringiensis serovar galleriae strain 4G5 plasmid pBMB267, complete sequence) position: , mismatch: 10, identity: 0.688

tttttcttatagaaaaacttatagctatcttg	CRISPR spacer
tttttcttattgaaaaatttatacgagtaaga	Protospacer
********** ******.*****   .*   .

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

1121099 : 1131699

Bacillus_phage(33.33%)

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

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_005402946.1\|1121099_1123241_+	type I secretion system permease/ATPase	W8CYL7	Bacillus_phage	4.4e-27	23.9
WP_004959644.1\|1123237_1124425_+	HlyD family type I secretion periplasmic adaptor subunit	NA	NA	NA	NA
WP_004953163.1\|1124518_1125121_+	YigZ family protein	A0A1X9I5T8	Streptococcus_phage	1.7e-21	33.9
WP_080630816.1\|1125113_1125725_+	acyltransferase	M1HKK6	Paramecium_bursaria_Chlorella_virus	1.2e-11	58.2
WP_004913328.1\|1125843_1126686_+	universal stress protein	A0A2H4J154	uncultured_Caudovirales_phage	4.5e-36	33.9
WP_004959635.1\|1126805_1127474_-	O-methyltransferase	W8CYT3	Bacillus_phage	8.3e-25	40.9
WP_171265940.1\|1127610_1128264_-	peptidase M15	NA	NA	NA	NA
WP_004639922.1\|1128446_1128776_-	ferredoxin family protein	NA	NA	NA	NA
WP_099948352.1\|1129041_1131699_-	DNA mismatch repair protein MutS	A0A1V0SC35	Catovirus	2.3e-38	22.6

DBSCAN-SWA_2

2666200 : 2734325

uncultured_Caudovirales_phage(79.49%)

portal,tRNA,terminase,head,tail,plate,integrase,capsid

attL 2707363:2707379|attR 2725685:2725701

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_004950367.1\|2666200_2667982_+\|tRNA	aspartate--tRNA ligase	A0A2K9KZX5	Tupanvirus	5.8e-17	20.7
WP_004908914.1\|2668143_2668365_+	hypothetical protein	NA	NA	NA	NA
WP_099949135.1\|2668370_2669243_+	lysophospholipid acyltransferase family protein	NA	NA	NA	NA
WP_004950362.1\|2669264_2670077_-	glycosyltransferase family 25 protein	NA	NA	NA	NA
WP_099949136.1\|2670385_2671294_+	glycosyl transferase	NA	NA	NA	NA
WP_099949137.1\|2671476_2672382_+	lipopolysaccharide biosynthesis protein	NA	NA	NA	NA
WP_099949138.1\|2672420_2674349_+	acyltransferase	A0A193GZ69	Enterobacter_phage	6.4e-62	37.7
WP_099949139.1\|2674352_2675264_-	hypothetical protein	NA	NA	NA	NA
WP_099949140.1\|2675318_2676077_-	glycosyltransferase family 25 protein	NA	NA	NA	NA
WP_099949141.1\|2676091_2677087_-	capsular polysaccharide biosynthesis protein	NA	NA	NA	NA
WP_099949142.1\|2677114_2677870_-	glycosyltransferase	A0A292GAQ8	Xanthomonas_phage	5.5e-09	25.7
WP_004950345.1\|2678036_2679197_-	nucleotide sugar dehydrogenase	M1I798	Paramecium_bursaria_Chlorella_virus	5.2e-99	47.8
WP_004950342.1\|2679339_2680266_-	branched-chain amino acid transaminase	NA	NA	NA	NA
WP_099949143.1\|2680292_2683040_-	bifunctional [glutamate--ammonia ligase]-adenylyl-L-tyrosine phosphorylase/[glutamate--ammonia-ligase] adenylyltransferase	NA	NA	NA	NA
WP_099949144.1\|2683112_2684384_-	HAMP domain-containing histidine kinase	W8CYF6	Bacillus_phage	9.5e-22	27.3
WP_099949145.1\|2684560_2685187_-	hypothetical protein	NA	NA	NA	NA
WP_099949147.1\|2686098_2687178_-\|portal	phage portal protein	A0A2H4JCD2	uncultured_Caudovirales_phage	4.0e-146	72.3
WP_099949148.1\|2687174_2688956_-\|terminase	terminase	A0A2H4J8R1	uncultured_Caudovirales_phage	4.7e-261	78.0
WP_099949149.1\|2689096_2690008_+\|capsid	GPO family capsid scaffolding protein	A0A2H4JGC7	uncultured_Caudovirales_phage	1.8e-78	54.2
WP_099949150.1\|2690022_2691051_+\|capsid	phage major capsid protein, P2 family	A0A2H4J8R3	uncultured_Caudovirales_phage	4.5e-155	76.6
WP_099949151.1\|2691053_2691878_+	hypothetical protein	A0A2H4JAI1	uncultured_Caudovirales_phage	3.8e-80	59.3
WP_099949152.1\|2691881_2692280_+\|head	head completion/stabilization protein	A0A2H4JFX3	uncultured_Caudovirales_phage	4.4e-42	70.5
WP_099949153.1\|2692276_2692480_+\|tail	tail protein X	A0A2H4JDW1	uncultured_Caudovirales_phage	1.1e-12	49.3
WP_099949154.1\|2692490_2692862_+	hypothetical protein	A0A2H4JFC0	uncultured_Caudovirales_phage	4.5e-41	68.3
WP_171265914.1\|2692871_2693393_+	secretion activator protein	A0A2H4J8Q8	uncultured_Caudovirales_phage	1.6e-79	79.8
WP_099949155.1\|2693395_2693788_+\|tail	phage tail protein	A0A2H4J8N7	uncultured_Caudovirales_phage	4.5e-47	66.2
WP_099949156.1\|2693791_2694229_+	phage virion morphogenesis protein	A0A2H4JCC1	uncultured_Caudovirales_phage	2.6e-56	73.6
WP_099949157.1\|2694225_2694339_+	Com family DNA-binding transcriptional regulator	NA	NA	NA	NA
WP_099949158.1\|2694381_2695230_+	DNA adenine methylase	A0A2H4J8Q1	uncultured_Caudovirales_phage	9.5e-127	77.3
WP_099949159.1\|2695310_2695838_+\|plate	phage baseplate assembly protein V	A0A2H4JGB7	uncultured_Caudovirales_phage	2.6e-66	69.5
WP_099949160.1\|2695837_2696209_+	GPW/gp25 family protein	A0A2H4J8P9	uncultured_Caudovirales_phage	3.3e-31	53.7
WP_099949161.1\|2696205_2697102_+\|plate	baseplate J/gp47 family protein	A0A2H4JAG9	uncultured_Caudovirales_phage	4.7e-116	72.2
WP_099949162.1\|2697094_2697616_+\|tail	phage tail protein I	A0A2H4JFW9	uncultured_Caudovirales_phage	1.4e-56	60.9
WP_099949163.1\|2698487_2698817_+	hypothetical protein	NA	NA	NA	NA
WP_099949164.1\|2698816_2700166_+	hypothetical protein	NA	NA	NA	NA
WP_099949165.1\|2700261_2700888_+	hypothetical protein	A0A2H4JFB5	uncultured_Caudovirales_phage	3.0e-61	59.3
WP_099949166.1\|2700953_2702828_+	BspA family leucine-rich repeat surface protein	NA	NA	NA	NA
WP_099949167.1\|2702963_2703590_+\|tail	phage tail sheath subtilisin-like domain-containing protein	A0A2H4J8M7	uncultured_Caudovirales_phage	2.0e-97	81.6
WP_099949168.1\|2703600_2704107_+\|tail	phage major tail tube protein	A0A2H4JCA8	uncultured_Caudovirales_phage	4.9e-78	79.2
WP_099949169.1\|2704152_2704497_+\|tail	phage tail assembly protein	A0A2H4J8P1	uncultured_Caudovirales_phage	2.9e-34	69.8
WP_099949524.1\|2704511_2704631_+\|tail	GpE family phage tail protein	NA	NA	NA	NA
WP_099949170.1\|2704627_2707210_+\|tail	phage tail tape measure protein	A0A2H4JGB2	uncultured_Caudovirales_phage	0.0e+00	69.7
WP_099949171.1\|2707220_2707628_+\|tail	phage tail protein	A0A2H4J8N8	uncultured_Caudovirales_phage	2.6e-50	72.5
2707363:2707379	attL	NA	NA	NA	NA
WP_099949525.1\|2707630_2708614_+	hypothetical protein	A0A2H4JAG0	uncultured_Caudovirales_phage	7.4e-139	76.2
WP_099949172.1\|2708685_2709102_-	antitoxin	A0A2H4JFV9	uncultured_Caudovirales_phage	1.8e-33	51.1
WP_099949173.1\|2709181_2709361_-	type II toxin-antitoxin system HicA family toxin	A0A2H4JDU5	uncultured_Caudovirales_phage	6.4e-09	50.8
WP_099949174.1\|2709528_2709714_+	hypothetical protein	NA	NA	NA	NA
WP_157774471.1\|2709884_2710256_+	hypothetical protein	NA	NA	NA	NA
WP_157774472.1\|2710339_2711308_-	hypothetical protein	NA	NA	NA	NA
WP_099949177.1\|2712978_2713173_+	hypothetical protein	NA	NA	NA	NA
WP_099949178.1\|2713169_2713349_+	hypothetical protein	A0A2H4J8L7	uncultured_Caudovirales_phage	1.7e-17	64.3
WP_099949179.1\|2713345_2714023_+	hypothetical protein	A0A2H4JC99	uncultured_Caudovirales_phage	9.4e-69	60.5
WP_099949180.1\|2714033_2714375_+	hypothetical protein	A0A2H4J8M9	uncultured_Caudovirales_phage	1.5e-35	68.6
WP_099949181.1\|2714358_2714580_+	hypothetical protein	A0A2H4JGA6	uncultured_Caudovirales_phage	3.3e-07	44.3
WP_099949182.1\|2714542_2714884_-	helix-turn-helix transcriptional regulator	A0A2H4J8M8	uncultured_Caudovirales_phage	8.8e-23	50.5
WP_157774473.1\|2714997_2715162_+	toxin-antitoxin system HicB family antitoxin	NA	NA	NA	NA
WP_099949183.1\|2715307_2715691_+	ogr/Delta-like zinc finger family protein	NA	NA	NA	NA
WP_099949184.1\|2715698_2718428_+	toprim domain-containing protein	A0A2H4JDT6	uncultured_Caudovirales_phage	0.0e+00	75.2
WP_099949185.1\|2718498_2718948_+	DUF2528 family protein	NA	NA	NA	NA
WP_099949186.1\|2718940_2719252_+	hypothetical protein	NA	NA	NA	NA
WP_099949188.1\|2719543_2719834_+	hypothetical protein	NA	NA	NA	NA
WP_099949189.1\|2719861_2720926_-\|integrase	site-specific integrase	A0A0R6PHH4	Moraxella_phage	3.8e-32	32.5
WP_099949190.1\|2721378_2722416_+\|tRNA	tRNA preQ1(34) S-adenosylmethionine ribosyltransferase-isomerase QueA	NA	NA	NA	NA
WP_099949191.1\|2722429_2723458_+	hypothetical protein	NA	NA	NA	NA
WP_099949192.1\|2723537_2724107_+	LemA family protein	NA	NA	NA	NA
WP_099949193.1\|2724269_2725400_+\|tRNA	tRNA guanosine(34) transglycosylase Tgt	A0A1B1IVQ4	uncultured_Mediterranean_phage	1.7e-94	48.5
WP_004908970.1\|2725511_2725841_+	preprotein translocase subunit YajC	NA	NA	NA	NA
2725685:2725701	attR	NA	NA	NA	NA
WP_099949194.1\|2725892_2727794_+	protein translocase subunit SecD	NA	NA	NA	NA
WP_099949195.1\|2727804_2728773_+	protein translocase subunit SecF	A0A1B1IVP7	uncultured_Mediterranean_phage	5.0e-31	31.2
WP_099949196.1\|2728851_2729508_-	4'-phosphopantetheinyl transferase superfamily protein	NA	NA	NA	NA
WP_004908978.1\|2729573_2730983_-	ribosome biogenesis GTPase Der	NA	NA	NA	NA
WP_099949197.1\|2731160_2732303_-	outer membrane protein assembly factor BamB	NA	NA	NA	NA
WP_099949198.1\|2732302_2733001_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_099949199.1\|2733032_2734325_-\|tRNA	histidine--tRNA ligase	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_CP024632

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection