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_CP036549	Bacteroides fragilis strain DCMSKEJBY0001B plasmid pBFS01_3, complete sequence	0 crisprs	NA	0	0	0	0
NZ_CP036546	Bacteroides fragilis strain DCMSKEJBY0001B chromosome, complete genome	2 crisprs	PD-DExK,RT,PrimPol,csa3,cas2,cas4,cas7,cas8b6,cas3,cas5,cas6,DEDDh,WYL	1	4	3	2
NZ_CP036548	Bacteroides fragilis strain DCMSKEJBY0001B plasmid pBFS01_2, complete sequence	0 crisprs	NA	0	0	0	0
NZ_CP036547	Bacteroides fragilis strain DCMSKEJBY0001B plasmid pBFS01_1, complete sequence	0 crisprs	Cas14u_CAS-V,c2c9_V-U4	0	0	0	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP036546_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036546_1

3058434-3058814

Orphan

Consensus_repeat	Method
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	CRISPRCasFinder
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	CRT
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	PILER-CR

5 spacers

The CRISPR arrays of NZ_CP036546_1

>merge|NZ_CP036546|1|3058434-3058814|CRISPRCasFinder,CRT,PILER-CR
ACCGTTAGCCTTATTATACTGGAATAGATCTACATTCTACAATTGGCTGGCAAAAAAAGCAATTGCCTTCGTCTTAATCCTTATTATACTGGAATAGATCTACATTGTAAGGAGCTATATTGGAATGAAGCTCCGGAAGTCTTAATCCTTATTATACTGGAATAGATCTACATACCAATGACACCATTACCTATGTAACCAAGAACGTCTTAATCCTTATTATACTGGAATAGATCTACATTGTTAAAGTAACCCTTGAAGGTGTTATGGCTTGGGTCTTAATCCTTATTATACTGGAATAGATCTACATTGATAAAAATTTTTCATGCCGCACAACGCATCGGGGGTCTTAATCCTTATTATACTGGAATAGATCTACAT

>NZ_CP036546|1|1|3058434-3058814|CRISPRCasFinder
ACCGTTAGCCTTATTATACTGGAATAGATCTACAT	TCTACAATTGGCTGGCAAAAAAAGCAATTGCCTTC
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGTAAGGAGCTATATTGGAATGAAGCTCCGGAA
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	ACCAATGACACCATTACCTATGTAACCAAGAAC
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGTTAAAGTAACCCTTGAAGGTGTTATGGCTTGG
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGATAAAAATTTTTCATGCCGCACAACGCATCGGGG
GTCTTAATCCTTATTATACTGGAATAGATCTACAT

>NZ_CP036546|1|1|3058434-3058814|CRT
ACCGTTAGCCTTATTATACTGGAATAGATCTACAT	TCTACAATTGGCTGGCAAAAAAAGCAATTGCCTTC
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGTAAGGAGCTATATTGGAATGAAGCTCCGGAA
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	ACCAATGACACCATTACCTATGTAACCAAGAAC
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGTTAAAGTAACCCTTGAAGGTGTTATGGCTTGG
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGATAAAAATTTTTCATGCCGCACAACGCATCGGGG
GTCTTAATCCTTATTATACTGGAATAGATCTACAT

>NZ_CP036546|1|1|3058504-3058814|PILER-CR
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGTAAGGAGCTATATTGGAATGAAGCTCCGGAA
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	ACCAATGACACCATTACCTATGTAACCAAGAAC
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGTTAAAGTAACCCTTGAAGGTGTTATGGCTTGG
GTCTTAATCCTTATTATACTGGAATAGATCTACAT	TGATAAAAATTTTTCATGCCGCACAACGCATCGGGG
GTCTTAATCCTTATTATACTGGAATAGATCTACAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036546.1\|WP_005808830.1\|3065640_3065865_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036546.1\|WP_032536431.1\|3051497_3052520_+\|polysaccharide-biosynthesis-protein	unknown	unknown	gnl\|CDD\|275003
NZ_CP036546.1\|WP_032536422.1\|3068956_3069766_+\|RNA-methyltransferase	unknown	unknown	gnl\|CDD\|223640
NZ_CP036546.1\|WP_032536427.1\|3063074_3064571_+\|glucose-6-phosphate-dehydrogenase	unknown	unknown	gnl\|CDD\|235579
NZ_CP036546.1\|WP_005808839.1\|3059602_3060082_+\|DUF4496-domain-containing-protein	unknown	unknown	gnl\|CDD\|273496
NZ_CP036546.1\|WP_032536432.1\|3050383_3051511_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340838
NZ_CP036546.1\|WP_032536430.1\|3052507_3053638_+\|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	unknown	unknown	gnl\|CDD\|340819
NZ_CP036546.1\|WP_032536423.1\|3066843_3068907_+\|family-10-glycosylhydrolase	unknown	unknown	gnl\|CDD\|187678
NZ_CP036546.1\|WP_033572629.1\|3049010_3050372_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373001
NZ_CP036546.1\|WP_032536425.1\|3064567_3065284_+\|6-phosphogluconolactonase	unknown	unknown	gnl\|CDD\|376480
NZ_CP036546.1\|WP_032536424.1\|3066087_3066402_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036546.1\|WP_005808835.1\|3061584_3063060_+\|decarboxylating-NADP(+)-dependent-phosphogluconate-dehydrogenase	unknown	unknown	gnl\|CDD\|236453
NZ_CP036546.1\|WP_032536428.1\|3055752_3056760_+\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|187543
NZ_CP036546.1\|WP_032536429.1\|3054518_3055730_+\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340825
NZ_CP036546.1\|WP_005786849.1\|3046724_3047870_+\|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	unknown	unknown	gnl\|CDD\|223458
NZ_CP036546.1\|WP_032536441.1\|3069871_3070294_-\|hydroxyisourate-hydrolase	unknown	unknown	gnl\|CDD\|376352
NZ_CP036546.1\|WP_005817163.1\|3053658_3054522_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187564
NZ_CP036546.1\|WP_032530624.1\|3056763_3057714_+\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|133464
NZ_CP036546.1\|WP_005808836.1\|3060273_3061452_-\|dicarboxylate/amino-acid:cation-symporter	unknown	unknown	gnl\|CDD\|366058
NZ_CP036546.1\|WP_032536241.1\|3047880_3048999_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|340825

Protein	Function_ID	Function_description	E-value
NZ_CP036546.1\|WP_032536431.1\|3051497_3052520_+\|polysaccharide-biosynthesis-protein	gnl\|CDD\|275003	TIGR04130, L-fucosamine_synthetase, UDP-N-acetylglucosamine 4,6-dehydratase/5-epimerase. The FnlA enzyme is the first step in the biosynthesis of UDP-FucNAc from UDP-GlcNAc in E. coli (along with FnlB and FnlC). The proteins identified by this model include FnlA homologs in the O-antigen clusters of O4, O25, O26, O29 (Shigella D11), O118, O145 and O172 serotype strains, all of which produce O-antigens containing FucNAc (or the further modified FucNAm). A homolog from Pseudomonas aerugiosa serotype O11, WbjB, also involved in the biosynthesis of UDP-FucNAc has been characterized and is now believed to carry out both the initial 4,6-dehydratase reaction and the subsequent epimerization of the resulting methyl group at C-5. A phylogenetic tree of related sequences shows a distinct clade of enzymes involved in the biosynthesis of UDP-QuiNAc (Qui=qinovosamine). This clade appears to be descendant from the common ancestor of the Pseudomonas and E. coli fucose-biosynthesis enzymes. It has been hypothesized that the first step in the biosynthesis of these two compounds may be the same, and thus that these enzymes all have the same function. At present, lacking sufficient confirmation of this, the current model trusted cutoff only covers the tree segment surrounding the E. coli genes. The clades containing the Pseudomonas and QuiNAc biosynthesis enzymes score above the noise cutoff. Immediately below the noise cutoff are enzymes involved in the biosynthesis of UDP-RhaNAc (Rha=rhamnose), which again may or may not produce the same product.	0
NZ_CP036546.1\|WP_032536422.1\|3068956_3069766_+\|RNA-methyltransferase	gnl\|CDD\|223640	COG0566, SpoU, rRNA methylases [Translation, ribosomal structure and biogenesis].	3.24257e-48
NZ_CP036546.1\|WP_032536427.1\|3063074_3064571_+\|glucose-6-phosphate-dehydrogenase	gnl\|CDD\|235579	PRK05722, PRK05722, glucose-6-phosphate 1-dehydrogenase; Validated.	0
NZ_CP036546.1\|WP_005808839.1\|3059602_3060082_+\|DUF4496-domain-containing-protein	gnl\|CDD\|273496	TIGR01201, HU_rel, DNA-binding protein, histone-like, putative. This model describes a set of proteins related to but longer than DNA-binding protein HU. Its distinctive domain architecture compared to HU and related histone-like DNA-binding proteins justifies the designation as superfamily. Members include, so far, one from Bacteroides fragilis, a gut bacterium, and ten from Porphyromonas gingivalis, an oral anaerobe. [DNA metabolism, Chromosome-associated proteins].	6.60941e-57
NZ_CP036546.1\|WP_032536432.1\|3050383_3051511_+\|glycosyltransferase	gnl\|CDD\|340838	cd03809, GT4_MtfB-like, glycosyltransferases MtfB, WbpX, and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. MtfB (mannosyltransferase B) in E. coli has been shown to direct the growth of the O9-specific polysaccharide chain. It transfers two mannoses into the position 3 of the previously synthesized polysaccharide.	3.31077e-27
NZ_CP036546.1\|WP_032536430.1\|3052507_3053638_+\|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	gnl\|CDD\|340819	cd03786, GTB_UDP-GlcNAc_2-Epimerase, UDP-N-acetylglucosamine 2-epimerase and similar proteins. Bacterial members of the UDP-N-Acetylglucosamine (GlcNAc) 2-Epimerase family (EC 5.1.3.14) are known to catalyze the reversible interconversion of UDP-GlcNAc and UDP-N-acetylmannosamine (UDP-ManNAc). The enzyme serves to produce an activated form of ManNAc residues (UDP-ManNAc) for use in the biosynthesis of a variety of cell surface polysaccharides; The mammalian enzyme is bifunctional, catalyzing both the inversion of stereochemistry at C-2 and the hydrolysis of the UDP-sugar linkage to generate free ManNAc. It also catalyzes the phosphorylation of ManNAc to generate ManNAc 6-phosphate, a precursor to salic acids. In mammals, sialic acids are found at the termini of oligosaccharides in a large variety of cell surface glycoconjugates and are key mediators of cell-cell recognition events. Mutations in human members of this family have been associated with Sialuria, a rare disease caused by the disorders of sialic acid metabolism. This family belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	1.6844e-142
NZ_CP036546.1\|WP_032536423.1\|3066843_3068907_+\|family-10-glycosylhydrolase	gnl\|CDD\|187678	cd09620, CBM9_like_3, DOMON-like type 9 carbohydrate binding module. Family 9 carbohydrate-binding modules (CBM9) play a role in the microbial degradation of cellulose and hemicellulose (materials found in plants). The domain has previously been called cellulose-binding domain. The polysaccharide binding sites of CBMs with available 3D structure have been found to be either flat surfaces with interactions formed by predominantly aromatic residues (tryptophan and tyrosine), or extended shallow grooves. CBM9 domains found in this uncharacterized heterogeneous subfamily may co-occur with various other domains.	9.99709e-72
NZ_CP036546.1\|WP_033572629.1\|3049010_3050372_+\|hypothetical-protein	gnl\|CDD\|373001	pfam14296, O-ag_pol_Wzy, O-antigen polysaccharide polymerase Wzy. This family includes O-antigen polysaccharide polymerases. These enzymes link O-units via a glycosidic linkage to form a long O-antigen. These enzymes vary in specificity and sequence.	0.000719993
NZ_CP036546.1\|WP_032536425.1\|3064567_3065284_+\|6-phosphogluconolactonase	gnl\|CDD\|376480	pfam01182, Glucosamine_iso, Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase.	1.14323e-75
NZ_CP036546.1\|WP_005808835.1\|3061584_3063060_+\|decarboxylating-NADP(+)-dependent-phosphogluconate-dehydrogenase	gnl\|CDD\|236453	PRK09287, PRK09287, NADP-dependent phosphogluconate dehydrogenase.	0
NZ_CP036546.1\|WP_032536428.1\|3055752_3056760_+\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|187543	cd05232, UDP_G4E_4_SDR_e, UDP-glucose 4 epimerase, subgroup 4, extended (e) SDRs. UDP-glucose 4 epimerase (aka UDP-galactose-4-epimerase), is a homodimeric extended SDR. It catalyzes the NAD-dependent conversion of UDP-galactose to UDP-glucose, the final step in Leloir galactose synthesis. This subgroup is comprised of bacterial proteins, and includes the Staphylococcus aureus capsular polysaccharide Cap5N, which may have a role in the synthesis of UDP-N-acetyl-d-fucosamine. This subgroup has the characteristic active site tetrad and NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they 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 numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, 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. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. 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.	9.91588e-56
NZ_CP036546.1\|WP_032536429.1\|3054518_3055730_+\|glycosyltransferase-family-4-protein	gnl\|CDD\|340825	cd03794, GT4_WbuB-like, Escherichia coli WbuB and similar proteins. This family is most closely related to the GT1 family of glycosyltransferases. WbuB in E. coli is involved in the biosynthesis of the O26 O-antigen. It has been proposed to function as an N-acetyl-L-fucosamine (L-FucNAc) transferase.	2.68105e-125
NZ_CP036546.1\|WP_005786849.1\|3046724_3047870_+\|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)	gnl\|CDD\|223458	COG0381, WecB, UDP-N-acetylglucosamine 2-epimerase [Cell envelope biogenesis, outer membrane].	6.71748e-175
NZ_CP036546.1\|WP_032536441.1\|3069871_3070294_-\|hydroxyisourate-hydrolase	gnl\|CDD\|376352	pfam00576, Transthyretin, HIUase/Transthyretin family. This family includes transthyretin that is a thyroid hormone-binding protein that transports thyroxine from the bloodstream to the brain. However, most of the sequences listed in this family do not bind thyroid hormones. They are actually enzymes of the purine catabolism that catalyze the conversion of 5-hydroxyisourate (HIU) to OHCU. HIU hydrolysis is the original function of the family and is conserved from bacteria to mammals; transthyretins arose by gene duplications in the vertebrate lineage. HIUases are distinguished in the alignment from the conserved C-terminal YRGS sequence.	2.12834e-48
NZ_CP036546.1\|WP_005817163.1\|3053658_3054522_+\|SDR-family-oxidoreductase	gnl\|CDD\|187564	cd05254, dTDP_HR_like_SDR_e, dTDP-6-deoxy-L-lyxo-4-hexulose reductase and related proteins, extended (e) SDRs. dTDP-6-deoxy-L-lyxo-4-hexulose reductase, an extended SDR, synthesizes dTDP-L-rhamnose from alpha-D-glucose-1-phosphate, providing the precursor of L-rhamnose, an essential cell wall component of many pathogenic bacteria. This subgroup has the characteristic active site tetrad and NADP-binding motif. This subgroup also contains human MAT2B, the regulatory subunit of methionine adenosyltransferase (MAT); MAT catalyzes S-adenosylmethionine synthesis. The human gene encoding MAT2B encodes two major splicing variants which are induced in human cell liver cancer and regulate HuR, an mRNA-binding protein which stabilizes the mRNA of several cyclins, to affect cell proliferation. Both MAT2B variants include this extended SDR domain. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they 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 numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, 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. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. 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.	6.98622e-86
NZ_CP036546.1\|WP_032530624.1\|3056763_3057714_+\|glycosyltransferase-family-4-protein	gnl\|CDD\|133464	cd06854, GT_WbpL_WbcO_like, The members of this subfamily catalyze the formation of a phosphodiester bond between a membrane-associated undecaprenyl-phosphate (Und-P) molecule and N-acetylhexosamine 1-phosphate, which is usually donated by a soluble UDP-N-acetylhexosamine precursor. The WbcO/WbpL substrate specificity has not yet been determined, but the structure of their biosynthetic end products implies that UDP-N-acetyl-D-fucosamine (UDP-FucNAc) and/or UDPN-acetyl-D-quinosamine (UDP-QuiNAc) are used. The subgroup of bacterial UDP-HexNAc:polyprenol-P HexNAc-1-P transferases includes the WbcO protein from Yersinia enterocolitica and the WbpL protein from Pseudomonas aeruginosa. These transferases initiate LPS O-antigen biosynthesis. Similar to other GlcNAc/MurNAc-1-P transferase family members, WbpL is a highly hydrophobic protein possessing 11 predicted transmembrane segments.	7.6108e-69
NZ_CP036546.1\|WP_005808836.1\|3060273_3061452_-\|dicarboxylate/amino-acid:cation-symporter	gnl\|CDD\|366058	pfam00375, SDF, Sodium:dicarboxylate symporter family.	1.4416e-79
NZ_CP036546.1\|WP_032536241.1\|3047880_3048999_+\|hypothetical-protein	gnl\|CDD\|340825	cd03794, GT4_WbuB-like, Escherichia coli WbuB and similar proteins. This family is most closely related to the GT1 family of glycosyltransferases. WbuB in E. coli is involved in the biosynthesis of the O26 O-antigen. It has been proposed to function as an N-acetyl-L-fucosamine (L-FucNAc) transferase.	3.45745e-09

>NZ_CP036546.1|WP_032530624.1|3056763_3057714_+|glycosyltransferase-family-4-protein
MYYLIILVLLFLVELFYFRIADKCNIIDKPNERSSHTRITLRGGGIIFFFGALAYFLTNQFEYPWFMLALTLITFISFVDDIRSTSQGLRLVFHFTAMALMFYQWGLFSLPWWTIVVALIVCTGIINAYNFMDGINGITGGYSLVVLAALAFINGVYVPFVEPALIYTMLCAVLVFNFFNFRKQAKCFAGDVGSVSIAFVILFLIGMLIIRTENFSWIVLLAVYGVDSVLTIIHRLMLHENIGLPHRKHLYQIMANELKIPHVVVSLVYMLVQAVVIAGYLLFPGNEYGYLSGTIIALSLVYILFMKRFFCLHQAK
>NZ_CP036546.1|WP_032536428.1|3055752_3056760_+|NAD-dependent-epimerase/dehydratase-family-protein
MNILITGAYGFVGTNLINNLKIKHNLYGLDIVCPTREGVLKTFCWKDIDPESFPLQTLPQFDAIIHLAGKAHDTKNQSAAQSYFDINTGLTQKIFDFFLESSAKKFIFFSSVKAAADSVVGDMLTEDVIPAPVGPYGESKIRAEEYIKEHCVFPAVSSCECSPFREMTSLTEKQVYILRPCMIHGPGNKGNLNLLYNVVKKGILWPLGDFENRRSFTSIDNLCYVIEGLLTKEVPTGIYHMGDDEALSTNELIAIMCEAMGKQPHIWKMNKGFMEGCAGLGTLLHLPLNTERLRKLTENYVVSNAKIKAALGIDKMPVTAKEGLIKTIRSFEETK
>NZ_CP036546.1|WP_032536429.1|3054518_3055730_+|glycosyltransferase-family-4-protein
MKILLVSQYFWPETFRVNDLAQELVLRGNEVTVLTGKPNYPQGAIYKGYSFWGYKKEYYKGIELIRVPLIPRGKGSGLRLALNYLSFVLFSCLYILFHKRKFDISLTFAISPITQVYAALLHKKLFGSRAYLWVQDLWPESVSAAGKMNSGLVYRMLTKMVQSIYQKVDGICIQSEAFSQSILQKGDYKHKISYIPNWAEDLFTDDSLINKEHFKSLIPDGFVVMFAGNIGEAQDFDSILKAAIRTKEYKDIKWVIVGDGRKKEFVEQQVKELNLCDTVFLLGRYPLEDMPDLFIHADVMLVSLKDQNIFSLTIPSKIQSYMAFGKPIISMINGIGNEIIKEANCGFTANAGDFESLANNVKRLSRMDKNMLYEKGRAGKEYYQLSFAKKKIIDNLIEVFQSE
>NZ_CP036546.1|WP_005817163.1|3053658_3054522_+|SDR-family-oxidoreductase
MVKKKILLFGATGMAGHMAYYYLQCTGKYDLVNVVYRTQLTDDSIVVDVTDGDAVSRLVREVRPDFILNCIGVLIRGSREHPDNAILINAWFPHLLKKLSDEVGAKLIHISTDCVFSGKKGNYSETDFRDADDVYGRSKALGEIINDKDLTIRTSIIGPELKENGEGLFHWFMHQHGCVNGFQTAIWGGVTTLELAKAIDVAIDQGVTGLIQLSNGLGISKYDLLHLFSRIWHKQDVEILPFDGNGIDKSIAKSARFSYVVPGYEEMLREQYDWMQNKQELYRTLYL
>NZ_CP036546.1|WP_032536430.1|3052507_3053638_+|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)
MLKVMTIVGTRPEIIKLSRVMAELDKYTEHIMVHTGQNFDYELNEIFFQELRIRKPDYFLDAAGKNAAETIANVIRKSDELMDQVKPDALLLYGDTNSCISVISAKRRKIPIFHMEAGNRCFDQRVPEEINRKIVDHLSDINMPLSEHARKYLLAEGLRPETVIKTGSPMTEVLIYHKAEIEENDVLEKEGLKKGDYFIVSTHREENVDSEKNFSDLLSSLNAIVDRYHKKVIVSTHPRTRKKLESIGFINSNPMIEFMKPFGFMEYIKLQQNAFCVISDSGTIMEESSILHFPAITIRQAHERPEGMDEGTLIMTGLNSDRILESIEIVTSQYAEGADVIHSIPDYASDNVSKKVVRIILSYTDYVNRTVWHKEI
>NZ_CP036546.1|WP_032536431.1|3051497_3052520_+|polysaccharide-biosynthesis-protein
MSIFKDKTLLITGGTGSFGNAVLKRFLDSDIKEIRIFSRDEKKQDDMRHHLQNKKVKFYIGDVRDKRSVDGVMNGVDYIFHAAALKQVPSCEFFPVQAVRTNVLGTENVLDSAIEHGVKNVVVLSTDKACYPINAMGISKAMMEKVAIAKGRQMGEGGQTTICCTRYGNVMASRGSVIPLWVEQMKAGKDITITDPNMTRFMMTLDDAVDLVIYAFQHGHNGDLFVQKAPAATLDTLARSLKELYKKDTPVRVIGTRHGEKLYESLVTREEMAKAEDMGNYYRIPCDARDLNYDKYFVEGQEKVSKFEDYHSHNTHRLDVDGMKQLLLKLDMIKEDVCLK
>NZ_CP036546.1|WP_032536432.1|3050383_3051511_+|glycosyltransferase
MKLIINASLNYVGGGLQVALSFIQECALIPENTYYVFMSENVSSQIDVTSYPTNFVFYNIPNLRFYQFHTYLSQIEREIVPDVVFSIFGPVYWKSRAPHIMGFALGHYLYSDSPFWGMVPWKDKLFWLIKKNIHFFFLKRDADAFITETEDATIRLAKLLHKPCFTVSNTYSRNFHSFKKDALLNDKILPNLEMDEYRLLSVSSAYPHKNLNIILPVIDVLHQKGFFNFKFVLTISQKEYLRLIPEIYRLVVVNVGPIPSQLVPQLYSECHATFVPSLLECFTANFPEAMIMRKPILASDLSFSHSICGDSALYFDPLDPIDIANSIIKLYRNPSLQEKLVNNGVERVNLFKTAAERAEMYLKICSKYINKNVHF
>NZ_CP036546.1|WP_033572629.1|3049010_3050372_+|hypothetical-protein
MHFTYAGIISLCVLFLIIVHVKGKIQTLVTLPLAMICVNFYNFYGRYESVEFSLRSEMLLLFSFLIFLISYSIGTRLVIKKSVSFINDIIHKENSNGDLLCKRSVFSFFIFIVFLYACFDLWLNTWLYGSFEAAMTRFYVRQTIDEAPSFLVNMQVFIMTTIISLIFVFRLFQNIYHKKTALIYIPIAILILISFPKGSRGATVSPILFLILADLFYVKFYSVKQLAFYSKRMFEYCSLIIVSCFLFFILTFIRGIELDDIADLYEHLSSFELSQGTEEYGESEKDLMLSDLQFTFDNYGSKISFLPVTYTLGTVLCNPIPRAIFPKKPIGFGTVLTEAKYGNNDYSVENLVKWRTSFAVGVAGEGWANGGLLGLFLYSVLMGVYSGYFSKLYFRFILSQNYLSVIIALLFFQCSGKFIRGDLLSGITQGIYPIILFIIIVQLVYRKKKIVHN
>NZ_CP036546.1|WP_032536241.1|3047880_3048999_+|hypothetical-protein
MEEMNVIIVHKNSINVEPPTQMVLQTLSDLGVSVKLITLSIDKYWELELHKRNIEYFSLNINRYLRGGKVSLISRLKIWLKYRMFVLRILKQLDTNFIIWFVNADSIAPLLCSNIFNRYKFIFHILETYENSIFYKYVIDKYAKYVYNMVVCEEHRAAIFNMWFNLNKYPIILPNKPYRLLEKEAAIEFVKEKSFPLYDAIQNNRKIILYQGVVSYDRNLLPAIKAVKELGNEFVFVIMGRDYGPLNDYIQSCPEIIYVPQISSPQHLYITSLAYIGILIYNPISLNQIFCAPNKIFEYSGYRVPMIGNNIPGLSIPFEKFMAGEVFDMQSTNSIKNKILKIKNSMEYYKMGAERLYTSVDTTSIIYNTLSI
>NZ_CP036546.1|WP_005786849.1|3046724_3047870_+|UDP-N-acetylglucosamine-2-epimerase-(non-hydrolyzing)
MKKVMLVFGTRPEAIKMAPLVRELKRKSHSVKVIVCVTGQHREMLDQVLHLFDIIPDYDLNIMKSGQDLYDVTTKVLLGMRGVLLNTHPDIVLVHGDTTTSVAAALAAFYQQIPVGHVEAGLRTYDIYSPWPEELNRQITSRIATFHFAPTQISKKNLLMEGVDEKDIIVTGNTVIDALYMIIDKIKSNKNLEIELCTKMKTVGYDVNRLKEGRKMILITGHRRENFGDGFVSICKAIEVLAKQNPEIDLVYPMHLNPNVRKPIHDIFDNEELSNIFFIEPLEYLSFVYLMEQAYLVLTDSGGIQEEAPGLGKPVLVMRDTTERPEALEAGTVRLVGTDYDKIISETTQLLNNSQYYNAMSKAVNPYGDGFACNRIIESLM
>NZ_CP036546.1|WP_005808839.1|3059602_3060082_+|DUF4496-domain-containing-protein
MPLFYRARQSQLKTKEGKKQWHLTLVKVGKMVTSQQLAEVIAEKSSLTPGDVHNVIRNLMTAMRKELLNSRSVRLEGLGTFTMKACTQGNGVDQEEEVNPNQVKALRCLFTAEYTRPAAIGTTRALLQGVEFQKASAIGGAINGGSGSGDGDIVDDPTA
>NZ_CP036546.1|WP_005808836.1|3060273_3061452_-|dicarboxylate/amino-acid:cation-symporter
MKKIHIGLLPRIIIAIILGIAIGNFLPTPLVRLFVTFNSIFGEFLNFSIPLIILGLVTIAIADIGKGAGRMLLVTALIAYGATLFSGFLSYFTGAAIFPSLITPGAPLDEVSEAQGILPYFSVAIPPLMNVMTALVLAFTLGLGLASLHSDALKNVARDFQEIIVRMISAVILPLLPIYIFGIFLNMTHSGQVFSILMVFIKIIGVIFILHIFLLVFQYCIAALFVRKNPFRLLGRMLPAYFTALGTQSSAATIPVTLEQTKKNGVSADIAGFVIPLCATIHLSGSTLKIVACALALMMMQGMPFDFSLFAGFIFMLGITMIAAPGVPGGAIMASLGILQSMLGFDESAQALMIALYIAMDSFGTACNVTGDGAIALIIDKIMGKRKTPESL
>NZ_CP036546.1|WP_005808835.1|3061584_3063060_+|decarboxylating-NADP(+)-dependent-phosphogluconate-dehydrogenase
MATQNKTDIGLIGLAVMGENLALNMESRGWSVSVYNRTVPGVEEGVVERFINGRAKGKHIEGFTDIEAFVESIALPRKIMMMVRAGSPVDELMEQLFPYLSPGDILIDGGNSNYEDTNRRVKLAESKGFLFVGAGVSGGEEGALNGASIMPGGSEKAWEEVKPILQSIAAKAPDGSPCCQWVGPAGSGHFVKMIHNGIEYGDMQLIAEAYWVMKELLDMTNEEMASVFTRWNEGKLRSYLIEITGNILRHKDKTGAYLIDKILDAAGQKGTGKWSVINAMELGMPLGLIATAVFERSLSAQKELRETAARQYQSKHSMAVYNKQDTEKEIFAALYASKLVSYAQGFAVLQRASDAFGWSLDLASIARMWRGGCIIRSVFLNDIAAAFEAKEKPKHLLLAPYFEEEIKGLLSGWKNLVAQAMREELPVPAFSSALNYFYSLVSADLPANLVQAQRDYFGAHTFERKDELRGVFFHENWTGHGGDTKSGTYNV
>NZ_CP036546.1|WP_032536427.1|3063074_3064571_+|glucose-6-phosphate-dehydrogenase
MSKFVMTIFGASGDLTKRKLMPALYSLYVAKRLPEEFEILGVGRTVYEDADYRAYIYSEMEKFVKPEEQSKEKMEAFVAHLHYLAIDPAVENGYAQLRLRIEELSGDSRPDDLLFYLATPPSLYGVIPLHLKSVHLNKGRARIIVEKPFGYDLESAEKLNKIYASVFDEHQIYRIDHFLGKETAQNLLAFRFANGIFEPLWNRNYIDYVEVTAVENLGIEQRGGFYDTTGALRDMVQNHLIQLVALTAMEPPAVFNADNFRNEVVKVYESLTPLTETDLSEHIVRGQYTAGGNKRGYREEKNISTDSRTETYIAMKLGISNWRWSGVPFYIRTGKQMPTKVTEIVVHFRETPHQMFHCAGGNCPRANKLILRLQPNEGIVLKFGMKVPGPGFEVKQVMMDFSYDQLGGVPSGDAYARLIEDCILGDQTLFTRSDAVEASWHFFDPILRYWNEHPEAPLYGYPAGTWGPLESEAMMHEHGADWTNPCKNLTNTDQYCEL
>NZ_CP036546.1|WP_032536425.1|3064567_3065284_+|6-phosphogluconolactonase
MKPYIFPSSIETARALILHLVKLMLDEPDKTFCIAFSGGSTPALMFDLWANEYTDITPWERLKVFWVDERCVPPENSDSNYGMMRSLLLSVVPIPYENVFRIQGEKNPKKEAARYSKLVMKEVPMENDFPVFDVVLLGAGNDGHTSSIFPGQEELLSTDHIYEANFNPNNGQKRIALTGLPILNARRIIFLITGKVKSPVVEDIFYSGDTGPAAYIAHHADNVELFMDNAAAEKVVSR
>NZ_CP036546.1|WP_005808830.1|3065640_3065865_+|hypothetical-protein
MEYKFDEQSVKELMEWAQTAQLPQELELSKAERIFDVKLCVESDLSCIRAHYPDAFYNPAITRLYRIREKLEEK
>NZ_CP036546.1|WP_032536424.1|3066087_3066402_+|hypothetical-protein
MKKVLVALVIVMGLGFSVVKADEPLKKKSAKVEQRDSREDFTPIEVNNLPEAVIDELSCEGALIKEAFMAYSRSEGKLYKVIILSSDFHEQAVFLNERGNILNR
>NZ_CP036546.1|WP_032536423.1|3066843_3068907_+|family-10-glycosylhydrolase
MKQIHLDCLAVKLFLFFSLFSLPSGAQSIFQKYDRFLTEPRSYVCYRVDGKLKIDGKLDEVSWQKAKSTAPFVDISGEGFPTPKYETTAKMLWDDEYLYVGAILQEDDIKARLTQRDTIIYYDNDFEVFIDPDWDGHNYFEIETNARGVIFDLMLDKPYRSGGNFMVQWDCPGLKLAIHREGTLNKSKDKDKYWSVEMAIPHKALTMNFNNPLKAGNCWRINFSRVQWLKAGGPEENWVWTPTGKVDMHMPDRWGYLFFADEAVGAPERTVALPYNTAVYKLLWAMFYAQQERYAKEKSYLRTEKDFFLTDAELKGLPQGAQISVDATRNTYQIAITVPGENKRYVINNEGRFWTEKIAPRQVKNWVWTRINKNKSEADYRQWFALLKECGISGVMFEGYDENLYRMCKEAGLEAHFWKWTMNRAELLNVHPDWFAVNRKGESTHDKPAYVDYYRFLCPNHEGVAQYLADDYVKIAHLPYVDGVHLDYVRFPDVVLPVSLWKNYGIEQTSEHFEYDYCYCEVCRAKFKAQTGRDPLELKYPMEDQSWINFRLDAITRVVDRITEAVKADGKAISAAVFPGPSMAKKMVRQDWGNWTLDAYFPMIYNGFYYEGPEWIGRSVQESVKTVDGRAKVYAGLMFPDIKNDFEKALDEAFDNGASGVSFFDGPSDEYLHKFKAYLDKKGLKTE
>NZ_CP036546.1|WP_032536422.1|3068956_3069766_+|RNA-methyltransferase
MPIIEISSLSHPGVEIFSTLTEAQLRNRLEPEKGLFIAESPKVIKVALDAGYEPLAILCEQKHITGDAANIIERCGDIPVYTGDRELLATLTGYVLTRGVLCAMRLPVPRSMEEVCRRARRIVIIDGVVDTTNIGAIFRSAAALGIDAVLLTRNSCSPLNRRAIRVSMGAVFLVPWTWLDGPLSDLARWGFRTVAMALTDNSISIDDPVLTTEPKLAIVMGTEGDGLSHERIAEADYVVRIPMSHGVDSLNVAAASAIAFWQLRAEKEY
>NZ_CP036546.1|WP_032536441.1|3069871_3070294_-|hydroxyisourate-hydrolase
MTQLIKKFSVIIILSLLPFSIYAQTESHQLSTHILDISKGEPAQGVDITLYKLNPSTPSQWKQIATGKTDVNGRISNFLPGIEDNTGIYMLKFYTEPYFLKQGLKSIYPFVEVIFRIEGKKHYHIPITMSANGYSTYRGN

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Crispr_ID: NZ_CP036546_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP036546_2

3935808-3937438

Unclear

Consensus_repeat	Method
GTTTCAATTCCATAAGGTACAATTAACAC	CRISPRCasFinder
GTTTCAATTCCATAAGGTACAATTAACAC	CRT
GTTTCAATTCCATAAGGTACAATTAACAC	PILER-CR

25 spacers

cas2,cas4,cas7,cas8b6,cas3,cas5,cas6

The CRISPR arrays of NZ_CP036546_2

>merge|NZ_CP036546|2|3935808-3937438|CRISPRCasFinder,CRT,PILER-CR
AGTCCAATTCCATAAGGTACAATTAATACCCTGTCATTTTATCTTTATTTTGCTTTTTTCTCAGGTTTCAATTCCATAAGGTACAATTAACACATCAAGTTTAAGTTCATCTCTCAGGAACGTTACTGTTTCAATTCCATAAGGTACAATTAACACTATTGAGCTACCGTTCCACTTCATCACTCCGACAGGTTTCAATTCCATAAGGTACAATTAACACAATGAGTAAATCTTTTTTAACCTTTATGATTCTATCGTTTCAATTCCATAAGGTACAATTAACACATCATCAACCACAGACGCATACTTAGACTTATTAAGTGTTTCAATTCCATAAGGTACAATTAACACGTTTTAGACAGTTTGTTTCTAAGAGCTGGCGATTGTTTCAATTCCATAAGGTACAATTAACACTTGATTGCAGAGGTTGACAAAAAACCTGTTTAATAGTTTCAATTCCATAAGGTACAATTAACACAAATTTGATGAAAAATGAGTAGTTTATTTTCGTAGTTTCAATTCCATAAGGTACAATTAACACTAAATTTGATGAAAAATGAGTAATTTGTTTTCGTAGTTTCAATTCCATAAGGTACAATTAACACGATGGATCGTTGGTCCCAAGACCCTGTTAAAGCTCGTGTTTCAATTCCATAAGGTACAATTAACACAACCACAAATACGGGTCGAACGATGTGCTTGCATGTTTCAATTCCATAAGGTACAATTAACACCATGAATAAAGCGTCTTTTCTTATAATAAATAAGCGTTTCAATTCCATAAGGTACAATTAACACGAGTAAAAACTAAAGACAATTAACGACCTCTACGTGTTTCAATTCCATAAGGTACAATTAACACAAACCGATCAGTAAAACGATCAATAACATGAAAGTGTTTCAATTCCATAAGGTACAATTAACACTCAACCGAAGTTCCTCAGGTGCATAATACAAAGAAGTTTCAATTCCATAAGGTACAATTAACACATATCGTGAATCAAAAGAATCACTTTTTTTAAAGGTTTCAATTCCATAAGGTACAATTAACACTTTTCTAAGCGTTTGTATTTTTTGATTCGTCGATATTGTTTCAATTCCATAAGGTACAATTAACACTTTGCCACAGGAAAAACAGATAGCTCTTTCTACTCTGTTTCAATTCCATAAGGTACAATTAACACCCTGTTTAGTTATGGAAGTTAAGAATTTTTATTTGTTTCAATTCCATAAGGTACAATTAACACGGTTATCGTTCTCGTTTTGTAAATCATGCTGTTGGGTTTCAATTCCATAAGGTACAATTAACACGAATTAACAATAAGAGGCTTACCAAAAGCACTACGTAAGTTTCAATTCCATAAGGTACAATTAACACGAAATACCACCTGCACGAATACCAGCCATAAAAGTGTTTCAATTCCATAAGGTACAATTAACACACCTCATCAATGAATCCGAACTTTGCAAGGACTTGGTTTCAATTCCATAAGGTACAATTAACACACAATTGTTAAACCTAAAAGGTCGCATATCAATGTTTCAATTCCATAAGGTACAATTAACACAACTAATTGAAGCAGAACCAGAAGCAGCATAATTGTTTCAATTCCATAAGGTACAATTAACAC

>NZ_CP036546|2|2|3935808-3937438|CRISPRCasFinder
AGTCCAATTCCATAAGGTACAATTAATAC	CCTGTCATTTTATCTTTATTTTGCTTTTTTCTCAG
GTTTCAATTCCATAAGGTACAATTAACAC	ATCAAGTTTAAGTTCATCTCTCAGGAACGTTACT
GTTTCAATTCCATAAGGTACAATTAACAC	TATTGAGCTACCGTTCCACTTCATCACTCCGACAG
GTTTCAATTCCATAAGGTACAATTAACAC	AATGAGTAAATCTTTTTTAACCTTTATGATTCTATC
GTTTCAATTCCATAAGGTACAATTAACAC	ATCATCAACCACAGACGCATACTTAGACTTATTAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	GTTTTAGACAGTTTGTTTCTAAGAGCTGGCGATT
GTTTCAATTCCATAAGGTACAATTAACAC	TTGATTGCAGAGGTTGACAAAAAACCTGTTTAATA
GTTTCAATTCCATAAGGTACAATTAACAC	AAATTTGATGAAAAATGAGTAGTTTATTTTCGTA
GTTTCAATTCCATAAGGTACAATTAACAC	TAAATTTGATGAAAAATGAGTAATTTGTTTTCGTA
GTTTCAATTCCATAAGGTACAATTAACAC	GATGGATCGTTGGTCCCAAGACCCTGTTAAAGCTCGT
GTTTCAATTCCATAAGGTACAATTAACAC	AACCACAAATACGGGTCGAACGATGTGCTTGCAT
GTTTCAATTCCATAAGGTACAATTAACAC	CATGAATAAAGCGTCTTTTCTTATAATAAATAAGC
GTTTCAATTCCATAAGGTACAATTAACAC	GAGTAAAAACTAAAGACAATTAACGACCTCTACGT
GTTTCAATTCCATAAGGTACAATTAACAC	AAACCGATCAGTAAAACGATCAATAACATGAAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	TCAACCGAAGTTCCTCAGGTGCATAATACAAAGAA
GTTTCAATTCCATAAGGTACAATTAACAC	ATATCGTGAATCAAAAGAATCACTTTTTTTAAAG
GTTTCAATTCCATAAGGTACAATTAACAC	TTTTCTAAGCGTTTGTATTTTTTGATTCGTCGATATT
GTTTCAATTCCATAAGGTACAATTAACAC	TTTGCCACAGGAAAAACAGATAGCTCTTTCTACTCT
GTTTCAATTCCATAAGGTACAATTAACAC	CCTGTTTAGTTATGGAAGTTAAGAATTTTTATTT
GTTTCAATTCCATAAGGTACAATTAACAC	GGTTATCGTTCTCGTTTTGTAAATCATGCTGTTGG
GTTTCAATTCCATAAGGTACAATTAACAC	GAATTAACAATAAGAGGCTTACCAAAAGCACTACGTAA
GTTTCAATTCCATAAGGTACAATTAACAC	GAAATACCACCTGCACGAATACCAGCCATAAAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	ACCTCATCAATGAATCCGAACTTTGCAAGGACTTG
GTTTCAATTCCATAAGGTACAATTAACAC	ACAATTGTTAAACCTAAAAGGTCGCATATCAAT
GTTTCAATTCCATAAGGTACAATTAACAC	AACTAATTGAAGCAGAACCAGAAGCAGCATAATT
GTTTCAATTCCATAAGGTACAATTAACAC

>NZ_CP036546|2|2|3935808-3937438|CRT
AGTCCAATTCCATAAGGTACAATTAATAC	CCTGTCATTTTATCTTTATTTTGCTTTTTTCTCAG
GTTTCAATTCCATAAGGTACAATTAACAC	ATCAAGTTTAAGTTCATCTCTCAGGAACGTTACT
GTTTCAATTCCATAAGGTACAATTAACAC	TATTGAGCTACCGTTCCACTTCATCACTCCGACAG
GTTTCAATTCCATAAGGTACAATTAACAC	AATGAGTAAATCTTTTTTAACCTTTATGATTCTATC
GTTTCAATTCCATAAGGTACAATTAACAC	ATCATCAACCACAGACGCATACTTAGACTTATTAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	GTTTTAGACAGTTTGTTTCTAAGAGCTGGCGATT
GTTTCAATTCCATAAGGTACAATTAACAC	TTGATTGCAGAGGTTGACAAAAAACCTGTTTAATA
GTTTCAATTCCATAAGGTACAATTAACAC	AAATTTGATGAAAAATGAGTAGTTTATTTTCGTA
GTTTCAATTCCATAAGGTACAATTAACAC	TAAATTTGATGAAAAATGAGTAATTTGTTTTCGTA
GTTTCAATTCCATAAGGTACAATTAACAC	GATGGATCGTTGGTCCCAAGACCCTGTTAAAGCTCGT
GTTTCAATTCCATAAGGTACAATTAACAC	AACCACAAATACGGGTCGAACGATGTGCTTGCAT
GTTTCAATTCCATAAGGTACAATTAACAC	CATGAATAAAGCGTCTTTTCTTATAATAAATAAGC
GTTTCAATTCCATAAGGTACAATTAACAC	GAGTAAAAACTAAAGACAATTAACGACCTCTACGT
GTTTCAATTCCATAAGGTACAATTAACAC	AAACCGATCAGTAAAACGATCAATAACATGAAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	TCAACCGAAGTTCCTCAGGTGCATAATACAAAGAA
GTTTCAATTCCATAAGGTACAATTAACAC	ATATCGTGAATCAAAAGAATCACTTTTTTTAAAG
GTTTCAATTCCATAAGGTACAATTAACAC	TTTTCTAAGCGTTTGTATTTTTTGATTCGTCGATATT
GTTTCAATTCCATAAGGTACAATTAACAC	TTTGCCACAGGAAAAACAGATAGCTCTTTCTACTCT
GTTTCAATTCCATAAGGTACAATTAACAC	CCTGTTTAGTTATGGAAGTTAAGAATTTTTATTT
GTTTCAATTCCATAAGGTACAATTAACAC	GGTTATCGTTCTCGTTTTGTAAATCATGCTGTTGG
GTTTCAATTCCATAAGGTACAATTAACAC	GAATTAACAATAAGAGGCTTACCAAAAGCACTACGTAA
GTTTCAATTCCATAAGGTACAATTAACAC	GAAATACCACCTGCACGAATACCAGCCATAAAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	ACCTCATCAATGAATCCGAACTTTGCAAGGACTTG
GTTTCAATTCCATAAGGTACAATTAACAC	ACAATTGTTAAACCTAAAAGGTCGCATATCAAT
GTTTCAATTCCATAAGGTACAATTAACAC	AACTAATTGAAGCAGAACCAGAAGCAGCATAATT
GTTTCAATTCCATAAGGTACAATTAACAC

>NZ_CP036546|2|2|3935872-3937438|PILER-CR
GTTTCAATTCCATAAGGTACAATTAACAC	ATCAAGTTTAAGTTCATCTCTCAGGAACGTTACT
GTTTCAATTCCATAAGGTACAATTAACAC	TATTGAGCTACCGTTCCACTTCATCACTCCGACAG
GTTTCAATTCCATAAGGTACAATTAACAC	AATGAGTAAATCTTTTTTAACCTTTATGATTCTATC
GTTTCAATTCCATAAGGTACAATTAACAC	ATCATCAACCACAGACGCATACTTAGACTTATTAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	GTTTTAGACAGTTTGTTTCTAAGAGCTGGCGATT
GTTTCAATTCCATAAGGTACAATTAACAC	TTGATTGCAGAGGTTGACAAAAAACCTGTTTAATA
GTTTCAATTCCATAAGGTACAATTAACAC	AAATTTGATGAAAAATGAGTAGTTTATTTTCGTA
GTTTCAATTCCATAAGGTACAATTAACAC	TAAATTTGATGAAAAATGAGTAATTTGTTTTCGTA
GTTTCAATTCCATAAGGTACAATTAACAC	GATGGATCGTTGGTCCCAAGACCCTGTTAAAGCTCGT
GTTTCAATTCCATAAGGTACAATTAACAC	AACCACAAATACGGGTCGAACGATGTGCTTGCAT
GTTTCAATTCCATAAGGTACAATTAACAC	CATGAATAAAGCGTCTTTTCTTATAATAAATAAGC
GTTTCAATTCCATAAGGTACAATTAACAC	GAGTAAAAACTAAAGACAATTAACGACCTCTACGT
GTTTCAATTCCATAAGGTACAATTAACAC	AAACCGATCAGTAAAACGATCAATAACATGAAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	TCAACCGAAGTTCCTCAGGTGCATAATACAAAGAA
GTTTCAATTCCATAAGGTACAATTAACAC	ATATCGTGAATCAAAAGAATCACTTTTTTTAAAG
GTTTCAATTCCATAAGGTACAATTAACAC	TTTTCTAAGCGTTTGTATTTTTTGATTCGTCGATATT
GTTTCAATTCCATAAGGTACAATTAACAC	TTTGCCACAGGAAAAACAGATAGCTCTTTCTACTCT
GTTTCAATTCCATAAGGTACAATTAACAC	CCTGTTTAGTTATGGAAGTTAAGAATTTTTATTT
GTTTCAATTCCATAAGGTACAATTAACAC	GGTTATCGTTCTCGTTTTGTAAATCATGCTGTTGG
GTTTCAATTCCATAAGGTACAATTAACAC	GAATTAACAATAAGAGGCTTACCAAAAGCACTACGTAA
GTTTCAATTCCATAAGGTACAATTAACAC	GAAATACCACCTGCACGAATACCAGCCATAAAAGT
GTTTCAATTCCATAAGGTACAATTAACAC	ACCTCATCAATGAATCCGAACTTTGCAAGGACTTG
GTTTCAATTCCATAAGGTACAATTAACAC	ACAATTGTTAAACCTAAAAGGTCGCATATCAAT
GTTTCAATTCCATAAGGTACAATTAACAC	AACTAATTGAAGCAGAACCAGAAGCAGCATAATT
GTTTCAATTCCATAAGGTACAATTAACAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP036546.1\|WP_005778065.1\|3927198_3927807_+\|thiamine-phosphate-synthase	unknown	unknown	gnl\|CDD\|238317
NZ_CP036546.1\|WP_005806448.1\|3938992_3939505_-\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|366863
NZ_CP036546.1\|WP_005806451.1\|3940640_3941966_-\|hypothetical-protein	cas8b6	mkCas0111_cas8b6_CAS-I-B	unknown
NZ_CP036546.1\|WP_005806458.1\|3945768_3946623_+\|type-I-methionyl-aminopeptidase	unknown	unknown	gnl\|CDD\|238519
NZ_CP036546.1\|WP_005806453.1\|3941969_3944129_-\|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|224124
NZ_CP036546.1\|WP_005778073.1\|3929372_3932093_-\|pyruvate,-phosphate-dikinase	unknown	unknown	gnl\|CDD\|236446
NZ_CP036546.1\|WP_005778086.1\|3935200_3935635_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036546.1\|WP_005806424.1\|3925295_3926420_+\|2-iminoacetate-synthase-ThiH	unknown	unknown	gnl\|CDD\|236425
NZ_CP036546.1\|WP_005778068.1\|3927887_3928403_-\|porin-family-protein	unknown	unknown	gnl\|CDD\|379226
NZ_CP036546.1\|WP_005806432.1\|3932359_3933778_+\|23S-rRNA-(uracil(1939)-C(5))-methyltransferase-RlmD	unknown	unknown	gnl\|CDD\|225174
NZ_CP036546.1\|WP_005778083.1\|3934774_3935179_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP036546.1\|WP_005806435.1\|3933788_3934706_+\|RluA-family-pseudouridine-synthase	unknown	unknown	gnl\|CDD\|223638
NZ_CP036546.1\|WP_005806450.1\|3939569_3940628_-\|hypothetical-protein	cas7	mkCas0088_cas7_CAS-I-B	gnl\|CDD\|187818
NZ_CP036546.1\|WP_005806429.1\|3928602_3929172_-\|PorT-family-protein	unknown	unknown	gnl\|CDD\|372635
NZ_CP036546.1\|WP_005806462.1\|3947876_3948623_+\|DUF169-domain-containing-protein	unknown	unknown	gnl\|CDD\|376845
NZ_CP036546.1\|WP_005806443.1\|3937651_3937915_-\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP036546.1\|WP_005806454.1\|3944118_3944682_-\|hypothetical-protein	cas5	mkCas0069_cas5_CAS-I-B	unknown
NZ_CP036546.1\|WP_005806426.1\|3926435_3927137_+\|HesA/MoeB/ThiF-family-protein	unknown	unknown	gnl\|CDD\|238386
NZ_CP036546.1\|WP_005806460.1\|3946623_3947850_+\|DNA-recombination-protein-RmuC	unknown	unknown	gnl\|CDD\|224241
NZ_CP036546.1\|WP_005806456.1\|3944693_3945365_-\|CRISPR-associated-endoribonuclease-Cas6	cas6	cd09652_cas6_CAS-I:CAS-III	gnl\|CDD\|273848

Protein	Function_ID	Function_description	E-value
NZ_CP036546.1\|WP_005778065.1\|3927198_3927807_+\|thiamine-phosphate-synthase	gnl\|CDD\|238317	cd00564, TMP_TenI, Thiamine monophosphate synthase (TMP synthase)/TenI. TMP synthase catalyzes an important step in the thiamine biosynthesis pathway, the substitution of the pyrophosphate of 2-methyl-4-amino-5- hydroxymethylpyrimidine pyrophosphate by 4-methyl-5- (beta-hydroxyethyl) thiazole phosphate to yield thiamine phosphate. TenI is a enzymatically inactive regulatory protein involved in the regulation of several extracellular enzymes. This superfamily also contains other enzymatically inactive proteins with unknown functions.	1.72829e-30
NZ_CP036546.1\|WP_005806448.1\|3938992_3939505_-\|CRISPR-associated-protein-Cas4	gnl\|CDD\|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	4.29989e-56
NZ_CP036546.1\|WP_005806458.1\|3945768_3946623_+\|type-I-methionyl-aminopeptidase	gnl\|CDD\|238519	cd01086, MetAP1, Methionine Aminopeptidase 1. E.C. 3.4.11.18. Also known as methionyl aminopeptidase and Peptidase M. Catalyzes release of N-terminal amino acids, preferentially methionine, from peptides and arylamides.	1.05797e-137
NZ_CP036546.1\|WP_005806453.1\|3941969_3944129_-\|CRISPR-associated-helicase/endonuclease-Cas3	gnl\|CDD\|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	1.04435e-61
NZ_CP036546.1\|WP_005778073.1\|3929372_3932093_-\|pyruvate,-phosphate-dikinase	gnl\|CDD\|236446	PRK09279, PRK09279, pyruvate phosphate dikinase; Provisional.	0
NZ_CP036546.1\|WP_005806460.1\|3946623_3947850_+\|DNA-recombination-protein-RmuC	gnl\|CDD\|224241	COG1322, COG1322, Predicted nuclease of restriction endonuclease-like fold, RmuC family [General function prediction only].	3.80603e-92
NZ_CP036546.1\|WP_005806424.1\|3925295_3926420_+\|2-iminoacetate-synthase-ThiH	gnl\|CDD\|236425	PRK09240, thiH, 2-iminoacetate synthase ThiH.	0
NZ_CP036546.1\|WP_005778068.1\|3927887_3928403_-\|porin-family-protein	gnl\|CDD\|379226	pfam13505, OMP_b-brl, Outer membrane protein beta-barrel domain. This domain is found in a wide range of outer membrane proteins. This domain assumes a membrane bound beta-barrel fold.	2.03152e-05
NZ_CP036546.1\|WP_005806432.1\|3932359_3933778_+\|23S-rRNA-(uracil(1939)-C(5))-methyltransferase-RlmD	gnl\|CDD\|225174	COG2265, TrmA, SAM-dependent methyltransferases related to tRNA (uracil-5-)-methyltransferase [Translation, ribosomal structure and biogenesis].	2.53299e-124
NZ_CP036546.1\|WP_005806435.1\|3933788_3934706_+\|RluA-family-pseudouridine-synthase	gnl\|CDD\|223638	COG0564, RluA, Pseudouridylate synthases, 23S RNA-specific [Translation, ribosomal structure and biogenesis].	9.63059e-68
NZ_CP036546.1\|WP_005806450.1\|3939569_3940628_-\|hypothetical-protein	gnl\|CDD\|187818	cd09687, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Cst2/DevR family.	2.86153e-06
NZ_CP036546.1\|WP_005806429.1\|3928602_3929172_-\|PorT-family-protein	gnl\|CDD\|372635	pfam13568, OMP_b-brl_2, Outer membrane protein beta-barrel domain. This domain is found in a wide range of outer membrane proteins. This domain assumes a membrane bound beta-barrel fold.	4.74368e-13
NZ_CP036546.1\|WP_005806462.1\|3947876_3948623_+\|DUF169-domain-containing-protein	gnl\|CDD\|376845	pfam02596, DUF169, Uncharacterized ArCR, COG2043.	4.73675e-28
NZ_CP036546.1\|WP_005806443.1\|3937651_3937915_-\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	2.15698e-27
NZ_CP036546.1\|WP_005806426.1\|3926435_3927137_+\|HesA/MoeB/ThiF-family-protein	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). .	1.28148e-115
NZ_CP036546.1\|WP_005806456.1\|3944693_3945365_-\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|273848	TIGR01877, CRISPR-associated_endoribonuclease_Cas6_1, CRISPR-associated endoribonuclease Cas6. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This broadly distributed, highly divergent Cas family is now characterized as an endoribonuclease that generates guide RNAs for host defense against phage and other invaders. The family contains a C-terminal motif GXGXXXXXGXG, where the each X between two Gly is hydrophobic and the spacer XXXXX contains (usually) one Arg or Lys. The seed alignment for the current version of this model has gappy columns removed. Members of this protein family are found associated with several different CRISPR/cas system subtypes, and consequently we designate this family Cas6.	2.18746e-23

>NZ_CP036546.1|WP_005778086.1|3935200_3935635_-|hypothetical-protein
MKTLNFMKTLLLLVAIVGLSSCGDKYYSDDYLRNSNAKLCGKTWVNDSDKNDADEWVRHTLKFDDSGRLAETYAYYHLNENQPYRTETNNLTWSWIDDSMEGIVFDYGVNGMTYFDNVWVREHNLSGKLNGKVVVFVDSKYNRN
>NZ_CP036546.1|WP_005778083.1|3934774_3935179_-|hypothetical-protein
MKGYLKILLVLLLAVGLASCEDDQGEIEYVIAGRAWTGDVGMNADNGEALFSTFEFGLDGFGVETQFYASDGALYDQYRFRWYWGDSYNRNLVLDYGTNGISFMDDVRVYGDRLSGIFYLSDNAPGFNFELRME
>NZ_CP036546.1|WP_005806435.1|3933788_3934706_+|RluA-family-pseudouridine-synthase
MKRMKRTPAEKARAQYTGYLVKEPMELMDFLAAKMPDASRTKLKSLLSKRIVLVDNVITTQFNFPLQPGMKVLISKDKNKKEFRHPLLKIVYEDAYIIVVEKKEGLLSVGTDRQKERTAQHILSEYVGRSGRGNRIFVVHRLDRDTSGLMMFAKDEKTQRTLRDHWHDIVTDRRYVAVVTGEMEKDSNTVVSWLTDRTLYVSSSSYDDGGSKSITHYRTIKRANGYSLVELRLETGRKNQIRVHMQDLGHPLIGDGRYGIDGGPNPLGRLALHAFKLCFYHPVTDQLMEFETPYPPAFKKLFLRK
>NZ_CP036546.1|WP_005806432.1|3932359_3933778_+|23S-rRNA-(uracil(1939)-C(5))-methyltransferase-RlmD
MARKKKELPLLEKVTITDVAAEGKAIAKVNDLVVFVPYVVPGDVVDLQVKRKKNKYAEAEAVKFHELSPIRAVPFCQHYGVCGGCKWQVLPYAEQIKYKQKQVEDNLRRIGKIELPEISPILGSAKTEFYRNKLEFTFSNKRWLTAEEVKQDVKYDQMNAVGFHIPGAFDKVLAIEKCWLQDDISNRIRNTIRDYAYEHNYSFINLRSQEGMLRNMIVRTSSTGELMVILICKITEEHEMDLFKQLLQYVADQFPEITSLLYIINNKCNDTINDLDVHVFRGNDHIFEEMEGLRFKVGPKSFYQTNSGQAYNLYKVARDFAGLTGGELVYDLYTGTGTIANFVSRQARQVIGIEYVPEAIEDAKVNAEINGIENTLFFAGDMKDILTQDFINQYGRPDVIITDPPRAGMHQDVVDVILFAEPKRIVYVSCNPATQARDLQLLDVKYRVKAVQPVDMFPHTHHVENVVLLELK
>NZ_CP036546.1|WP_005778073.1|3929372_3932093_-|pyruvate,-phosphate-dikinase
MDKKRVYTFGNGLAEGKAGMRNLLGGKGANLAEMNLIGVPVPPGFTITTDVCTEYYEMGQEKVVSLLKEEVEKAIANIENLMRSKFGDVENPLLVSVRSGARASMPGMMDTILNLGLNDEVVEGLTRKTGNARFAWDSYRRFVQMYGDVVLGMKPVNKEDQDPFEAIIEEVKHAKGVKLDNELEVEDLKELVKKFKAAVKAQTGKDFPTCAYEQLWGAICAVFNSWMNERAILYRKMEGIPDEWGTAVSVQAMVFGNMGDGSATGVCFSRDAATGEDLFNGEYLINAQGEDVVAGIRTPQQITKIGSQRWAQLAGVSEEERASKYPSMEEAMPEIYKQLDELQTKLENHYKDMQDMEFTVQEGKLWFLQTRNGKRTGAAMVKIAMDLFRQGMIDEKTALMRVEPNKLDELLHPVFDKSALKQAKVLTRGLPASPGAATGQIVFFADDAAEWHAAGKRVVMVRIETSPEDLAGMAVAEGILTARGGMTSHAAVVARGMGKCCVSGAGALNIDYKARTVEVDGVLLKEGDFISLNGSTGEVYQGKVETKAAELSGDFSDLMKLADKYTRLQVRTNADTPHDAEVARNFGAVGIGLCRTEHMFFEGEKIKAMREMILAENAEGRRKALAKILPYQQADFKGIFKAMSGCPVTVRLLDPPLHEFVPHDLKGQQEMADTMGVSLQYIQQRVESLCEHNPMLGHRGCRLGNTYPEITQMQTRAILGAALELKKEGIETHPEIMVPLTGILYEFQQQESVIRAEAEKLFEEVGDRIDFKVGTMIEIPRAALTADRIASSAEFFSFGTNDLTQMTFGYSRDDIASFLPVYLEKKILKVDPFQVLDQNGVGQLVRMATEKGRAIRPDLKCGICGEHGGEPSSVKFCHKVGLNYVSCSPFRVPIARLAAAQAAIED
>NZ_CP036546.1|WP_005806429.1|3928602_3929172_-|PorT-family-protein
MKRNLVFVLFALFSVVGFSQVSWNAKVGMNISNYTGDFDMNAKVGFKIGGGMEYGFNEIWSLQPSLFVSSKGVKKDELSVNAVYLELPVMAAARFKVADNTNIVLSAGPYFACGIGGNSKVDLGKGRLEVDTFGDDGLLKRGDVGLGIGVAAEFGKIIAGLDGQFGFVDVMDDVNGKNLNVSISVGYKF
>NZ_CP036546.1|WP_005778068.1|3927887_3928403_-|porin-family-protein
MKKIVLFLFVAIATLSVKAQDIYMGGTVGLWRNDDANTTSFKLAPEIGYNLSEQWALGVELQFNHDYISHKTINSFAIAPYARFSYYENKIVRLFIDGGFGFATTKVKDGGDAINGFEIGLKPGIAIKLNQHFSLVAKCGFLGYKDDYMNNSGFGFSASSEDLTFGFHYEF
>NZ_CP036546.1|WP_005778065.1|3927198_3927807_+|thiamine-phosphate-synthase
MKLIVVTTPTFFVEEDKIITALFEEGLDILHLRKPETPAMYSERLLTLIPEKYHKRIVTHEHFYLKEEFNLMGIHLNARNPKEPHDYSGHISCSCHSVEEVKNKKHFYDYVFMSPIYDSISKEGYNSPYTAEELRQAGKDKIIDGKVMALGGITPENILEVKDFGFGGAVVLGDLWGKFDACSDRDYLAVIEHFKKLKKMAD
>NZ_CP036546.1|WP_005806426.1|3926435_3927137_+|HesA/MoeB/ThiF-family-protein
MERYNRQIMLPEIGEAGQAKLKAAKVLIVGVGGLGSPIALYLAGAGVGTIGLVDNDEVSLSNLQRQVLYTEEEVGDLKAICASLRLSALNREIEVNACPGRLSKDNARELIRQYDIVVDGCDNFITRYLINDVCVELGKPYVYGAICGFEGQVSVFNYGSGAQRKTYRDLYPDEEEMLRMPPPPKGVVGVTPAVTGSVEATEVLKIICGFGEVLAGKLWTIDLRTLQSNIFSL
>NZ_CP036546.1|WP_005806424.1|3925295_3926420_+|2-iminoacetate-synthase-ThiH
MFSDELEKISWEETTKIIYSKTDADVRRALSKEHCDVNDFMALISPAAAPYLETMARLSRKYTLERFGKTISMFVPLYITNSCTNSCVYCGFNHNNPMKRTILTEEEMVNEYKAIKKLAPFENLLLVTGENPAKAGVDYIERALLLAKPYFSNLQIEVMPLKAEEYERLTYAGLNGVICFQETYNKANYKVYHPRGMKSKFEWRVNGFDRMGQAGVHKIGMGVLIGLEEWRTDVTMMAYHLRYLQKHYWKTKYSVNFPRMRPSENGGFQPNVVMNDRELAQVTFAMRIFDHDVDISYSTRESAEFRNHMATLGVTTMSAESKTEPGGYFTYPQALEQFHVSDERKAVEVDAALRSLGRIPVYKDWDTALTLTQC
>NZ_CP036546.1|WP_005806443.1|3937651_3937915_-|CRISPR-associated-endonuclease-Cas2
MYVILVYDFGERRVSKMLRLCRRYLNWIQNSVFEGELSEVRLKELLLLAKGFMNPEEDCIIIFKGATQCSLEKEIVGKELSNIDNFL
>NZ_CP036546.1|WP_005806448.1|3938992_3939505_-|CRISPR-associated-protein-Cas4
MNLIGTHFNYYQVCKRKLWLFANGIRMEHTSDLVYDGKLIHENSYPQRSSKYEEIEIDGIKVDYYDALHKTIHEIKKSDKVDIAHEWQLKYYIYVFERNGIMDVTGVLEYPILRKRNIVLLSEIDREKISEMETDIIRIMDSDICPSLERKRICRNCSYFDFCYSGEDVE
>NZ_CP036546.1|WP_005806450.1|3939569_3940628_-|hypothetical-protein
MKPYIYLRGLRHVDLSVFCVENGQKRYWDPVFNVWAPYSSGQQVKRSILNAINDELQAEPSPVTFVFDVNKNTLGEGEVLSLCDPQYFDQLLGGWMKAAKGGKERTLKRRSPFSISAMRPLHPLLGGRFIENATFDRSDRPELHKVIVRDSSGKPMTEEQIEELLVDTDRSLYRKWIPENSRATGLFVYDVAIDMRTLFTVSTNQLEPELSKEKIQELKEKGWGITQNVFGECLIMPEVERLKVIPAIAKALVNWRISSNQSRTFSLMETLAVAISDNANTLAGAIRAKLLDNNPDKPQAKPVIDEAAGAELFVTLPCSGYVVTENESADALQKAEAKLIALLTAFDYETQK
>NZ_CP036546.1|WP_005806451.1|3940640_3941966_-|hypothetical-protein
MYTTTIGKIFLKAYNRKYQKEHTGKSFFIEEFVPLFFDHQKYMMTAGNSPLENPKLSWEDMIKGKKPFETPEQRQARIDKMIRKIESEEADASIAVGYGVSDNTAATTGQVTNIDFPDNKENIYLSWIGAGLGVGVSGGLTISFNHEQILLDIFDGWKYYRDYLERYPWMKGNQINTWNAHWITHRYDDYLYDVDNPTSGMNPVVSVEGEIVNLPTISWVPVVMGIARYFPIDNLVGYLYSIGQSNTTIGFMPFRLQDIISIEHLYSKVFGLPALNDNRRKIESLLGTAFGLRIACQAGTIGIPAMEPKGLKAYFSTGKGLKKIVYKDDNEQKIIINIYLIWILAMLNNEKLWTLSEEFARLLLQYEADAGKMKRDRMNQVGQLFASVSAKQFLNNLIPIIENEKEVEGYRNMGKVLHEMPKDNFPYFNTLIRFQYALLNK
>NZ_CP036546.1|WP_005806453.1|3941969_3944129_-|CRISPR-associated-helicase/endonuclease-Cas3
MGSRYDYILAKSESNGGTPLKSHLESVAFFAQIAARYAGMDENVVKIGALLHDIGKASPLFQARLKGEKTPYEKVFRHEVASLFFLKLIERSLWPEVIDMIIAHHKSVYKDRSSSGLLDLKDYYGEENTFSDHVAGFPSWNVDAIGILRELNFPGLSADSLLSEEDALEAYRYAIEHCRRKPKGWSKWKGLLMGVDHLASATEEFKERIPTLFSIPDVGFYNRQHPLYPLSQVLSEANKKHTFVKAPTGAGKTDFLLKRCQGRIFYTLPFQASINAMYERIHRDLNGMVEDVRLLHSMSRLVIEGEKAWEEKVIQDKIGASIKVLTPHQLASVSLGTKGYETLLFDLCGCDIILDEIHTYSDIMQSIILTMIEVLVHIGCRIHVGTATMPSELEQKILDILGRDKTQQVELLPSVLDSFNRHIVHKVTDFDSVLPVLREAIENDQKILIVCNRVRNAQILFERIDELYPEVDKMLIHSRFKRKDRNRLEKELQDTYNKMPRACIVVSTQVVEVSLDISFDMMITETAPIDALIQRFGRINRKRKPKEERTLKHIYVIAPPDKKEDCLPYSQEILQRSYDALPQDSLLEESSLQRLIDQVYPQVNVIDLSLDAAFADGKWRLKELFHLPKSAFIEKLDIDSVSCITQEDADTGKYREATAEERILMEIPMRYSSLRWKKLETFPYGSHPFVIPDIAYSSDRGLDVTKMGAENYDTNYQML
>NZ_CP036546.1|WP_005806454.1|3944118_3944682_-|hypothetical-protein
MKYYVVKYAGPFGFIKPWTAVRDASGGETYSQQFLTPSIIEGIRQKLEVTAIMRHKLSYAGIDLQQEVVQAKAWSKKGKTYVKERSILRRGVMLSPVIYIAFSTLEDACKASLQHICLCRNEDILLPESNIQELSISEFDKLEGYELRFGESEQSFLVGYNRFKNNEEMYGWIEIVGNPTKVHKYGE
>NZ_CP036546.1|WP_005806456.1|3944693_3945365_-|CRISPR-associated-endoribonuclease-Cas6
MRIRIETTSSKKILPFDYQGKLIGVIHKWLGNNELHDKISLYSFSWLLGGVMVNKKGYIFPNGAELLISFYEDQYLKKIIDSILLDPEIFYGLCVKDITIVESSIFTEGPQRFFLASPIFIKRRIEEGIGYKYYFYDDLESNQLMTETLKHKMREAGLPEDDTLRVEFDISYSKKKKKMVTIHGIKSIANMCPVIIHGTQTSKRFAWVVGLGNGTGSGYGALI
>NZ_CP036546.1|WP_005806458.1|3945768_3946623_+|type-I-methionyl-aminopeptidase
MKKFIKGVRFTPSNYPDEIEDKIQKYRKQGYKLPPRKVLRTPEQIEGIRESAKINTALLDHIAENIREGMPTEEIDRLVYDFTTAHGAIPAPLNYEGFPKSVCTSINDVVCHGIPSPTEFLQSGDIVNVDVSTIYKGYFSDASRMFMIGEVSPEKQRLVQVTRECMEIGIAAAQPWARLGDVGAAIQEHAEKNGYSVVRDLCGHGVGIKFHEEPDVEHFGRRGTGMLILPGMTFTIEPMINMGTYEVFVDSADDWTVCTDDGLPSAQWENMILITETGNEILTY
>NZ_CP036546.1|WP_005806460.1|3946623_3947850_+|DNA-recombination-protein-RmuC
MELTLLLIIAALLVVQLVLTLTRNNRSQSEEMQRALRQQMQENREELNRSIRELRMEMTQTLNQGLQQLQDAMHKNMMTTGELQRQKFDAMARQQETLIQSTEKRLDDMRVMVEEKLQKTLNERIGHSFEIVRSQLENVQKGLGEMKSLAQDVGGLKKVLSNVKMRGTFGEVQLGALLEQMMSPEQYEANVKTKKSGTEFVEFAIKLPGKDDANSTVYLPIDAKFPKDVYEQYYDAFEAGDAVLMESCGRQLETTIKKMAKDIHDKYVDPPFTTDFAILFLPFESIYAEVIRRTTLVETLQKDFKIVVTGPTTLGAILNSLQMGFRTLAIQKRTGEVWTVLGAVKTEFGKFGGLLEKVQKNLQSAGDQLEEVMGKRTRAIERKLRQVEELPHEESRKILPIDDGGEDD
>NZ_CP036546.1|WP_005806462.1|3947876_3948623_+|DUF169-domain-containing-protein
METTLKDQFITLWDTYFPQAGLPIAFEYSADTQNLPVVEAPKGHRCIIAQLTQVQRGKTLCIQADSVGCRGGKRYTSFTDKMFPGFECFLSHNGQGEGERYKQTPELAAEALAQLPVLPIKGENLIFKRWDKLEAEDTPEAVIFFASADVLSGLFTLACFDNADPDAVIAPFGAGCASIIYHPYREQLNGTNRAVLGSFDPSARKCMKSDLLSFAIPFNKFKKMVLQIEESFLKTATWDVIKKRMGSS

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP036546_1	1.2\|3058539\|33\|NZ_CP036546\|CRISPRCasFinder,CRT,PILER-CR	3058539-3058571	33	NZ_CP036546.1	3204945-3204977	0	1.0

1. spacer 1.2|3058539|33|NZ_CP036546|CRISPRCasFinder,CRT,PILER-CR matches to position: 3204945-3204977, mismatch: 0, identity: 1.0

tgtaaggagctatattggaatgaagctccggaa	CRISPR spacer
tgtaaggagctatattggaatgaagctccggaa	Protospacer
*********************************

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP036546_2	2.16\|3936798\|34\|NZ_CP036546\|CRISPRCasFinder,CRT,PILER-CR	3936798-3936831	34	NZ_LR135199	Enterococcus faecium isolate E6055 plasmid 3	52997-53030	9	0.735
NZ_CP036546_2	2.16\|3936798\|34\|NZ_CP036546\|CRISPRCasFinder,CRT,PILER-CR	3936798-3936831	34	NZ_LR135374	Enterococcus faecium isolate E8172 plasmid 3	87168-87201	9	0.735
NZ_CP036546_2	2.1\|3935837\|35\|NZ_CP036546\|CRISPRCasFinder,CRT	3935837-3935871	35	NC_013940	Deferribacter desulfuricans SSM1 megaplasmid pDF308, complete sequence	252375-252409	10	0.714
NZ_CP036546_2	2.16\|3936798\|34\|NZ_CP036546\|CRISPRCasFinder,CRT,PILER-CR	3936798-3936831	34	LR721753	Aliivibrio wodanis 06/09/160 plasmid 2 complete sequence	188641-188674	10	0.706
NZ_CP036546_2	2.19\|3936992\|34\|NZ_CP036546\|CRISPRCasFinder,CRT,PILER-CR	3936992-3937025	34	NZ_CP039703	Clostridium butyricum strain 29-1 plasmid p-butyl_plas_29-1, complete sequence	202491-202524	10	0.706
NZ_CP036546_2	2.25\|3937376\|34\|NZ_CP036546\|CRISPRCasFinder,CRT,PILER-CR	3937376-3937409	34	NC_048646	Cronobacter phage vB_CsaM_leE, complete genome	169097-169130	10	0.706
NZ_CP036546_2	2.1\|3935837\|35\|NZ_CP036546\|CRISPRCasFinder,CRT	3935837-3935871	35	MK496714	Capybara microvirus Cap1_SP_121, complete genome	2516-2550	11	0.686

1. spacer 2.16|3936798|34|NZ_CP036546|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LR135199 (Enterococcus faecium isolate E6055 plasmid 3) position: , mismatch: 9, identity: 0.735

atatcgtgaatcaaaagaatcactttttttaaag	CRISPR spacer
ttattcgaaattaaaataatcactttttttaatt	Protospacer
 ***.  .***.**** ***************

2. spacer 2.16|3936798|34|NZ_CP036546|CRISPRCasFinder,CRT,PILER-CR matches to NZ_LR135374 (Enterococcus faecium isolate E8172 plasmid 3) position: , mismatch: 9, identity: 0.735

atatcgtgaatcaaaagaatcactttttttaaag	CRISPR spacer
ttattcgaaattaaaataatcactttttttaatt	Protospacer
 ***.  .***.**** ***************

3. spacer 2.1|3935837|35|NZ_CP036546|CRISPRCasFinder,CRT matches to NC_013940 (Deferribacter desulfuricans SSM1 megaplasmid pDF308, complete sequence) position: , mismatch: 10, identity: 0.714

cctgtcattttatctttattttgcttttttctcag	CRISPR spacer
aacctcattttttctttattttacttttttatatc	Protospacer
  . ******* **********.******* *

4. spacer 2.16|3936798|34|NZ_CP036546|CRISPRCasFinder,CRT,PILER-CR matches to LR721753 (Aliivibrio wodanis 06/09/160 plasmid 2 complete sequence) position: , mismatch: 10, identity: 0.706

atatcgtgaatcaaaagaatcactttttttaaag	CRISPR spacer
gtcatttgaatcaaaagaatcaccttatttacct	Protospacer
.*  . *****************.** ****

5. spacer 2.19|3936992|34|NZ_CP036546|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039703 (Clostridium butyricum strain 29-1 plasmid p-butyl_plas_29-1, complete sequence) position: , mismatch: 10, identity: 0.706

---cctgtttagttatggaagttaagaatttttattt	CRISPR spacer
gagtacgt---gttatggaagataagaattttgatga	Protospacer
   . .**   ********** ********** **

6. spacer 2.25|3937376|34|NZ_CP036546|CRISPRCasFinder,CRT,PILER-CR matches to NC_048646 (Cronobacter phage vB_CsaM_leE, complete genome) position: , mismatch: 10, identity: 0.706

aactaattgaagcagaaccagaagcagcataatt	CRISPR spacer
tcggcattgaagcagatccagcagcagcaccagt	Protospacer
     *********** **** *******. * *

7. spacer 2.1|3935837|35|NZ_CP036546|CRISPRCasFinder,CRT matches to MK496714 (Capybara microvirus Cap1_SP_121, complete genome) position: , mismatch: 11, identity: 0.686

cctgtcattttatctttattttgcttttttctcag	CRISPR spacer
atggcttttttatcttcatttttcttttttctttt	Protospacer
 . *.. *********.***** *********.

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

413259 : 475296

unidentified_phage(25.0%)

integrase,protease,transposase

attL 408969:408983|attR 479594:479608

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
408969:408983	attL	NA	NA	NA	NA
WP_005782309.1\|413259_414507_-\|protease	ATP-dependent Clp protease ATP-binding subunit ClpX	G3M9Z9	Bacillus_virus	2.2e-116	53.7
WP_005782306.1\|414509_415172_-	ATP-dependent Clp endopeptidase proteolytic subunit ClpP	A0A223W000	Agrobacterium_phage	9.6e-42	46.6
WP_032529761.1\|415311_416667_-	trigger factor	NA	NA	NA	NA
WP_005811280.1\|417906_418152_+	RNA-binding protein	NA	NA	NA	NA
WP_005782293.1\|418267_419029_-	LPS export ABC transporter ATP-binding protein	A0A2H4PQG7	Staphylococcus_phage	5.2e-23	28.0
WP_005782292.1\|419104_419848_+	ABC transporter permease	NA	NA	NA	NA
WP_005782291.1\|419844_420615_+	ABC transporter ATP-binding protein	F2Y1V5	Organic_Lake_phycodnavirus	1.3e-10	30.9
WP_005782290.1\|420847_421495_-	response regulator transcription factor	NA	NA	NA	NA
WP_005782289.1\|421671_422985_-	ribosome biogenesis GTPase Der	NA	NA	NA	NA
WP_005782288.1\|423037_423919_-	GTPase Era	NA	NA	NA	NA
WP_005811282.1\|424006_425011_-	ketoacyl-ACP synthase III	NA	NA	NA	NA
WP_002562387.1\|425109_425295_-	50S ribosomal protein L32	NA	NA	NA	NA
WP_080714160.1\|425308_425845_-	DUF177 domain-containing protein	NA	NA	NA	NA
WP_032536193.1\|432718_433495_+\|integrase	site-specific integrase	NA	NA	NA	NA
WP_008768950.1\|433510_433696_-	hypothetical protein	NA	NA	NA	NA
WP_004289225.1\|433924_434818_+	tyrosine recombinase	NA	NA	NA	NA
WP_004289226.1\|434864_435194_+	hypothetical protein	NA	NA	NA	NA
WP_004289228.1\|435927_436845_+	DUF4465 domain-containing protein	NA	NA	NA	NA
WP_004293827.1\|436909_438691_+	cell surface protein	NA	NA	NA	NA
WP_004311297.1\|438705_440796_+	lipoprotein	NA	NA	NA	NA
WP_004293828.1\|440824_441925_+	YncE family protein	NA	NA	NA	NA
WP_004311295.1\|441943_444022_+	TonB-dependent receptor plug domain-containing protein	NA	NA	NA	NA
WP_004289233.1\|444033_445173_+	ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_004311292.1\|445173_446154_+	iron ABC transporter permease	NA	NA	NA	NA
WP_008768949.1\|446117_446909_+	ABC transporter ATP-binding protein	A0A1V0SE00	Indivirus	6.2e-11	27.1
WP_004289236.1\|446905_447472_+	hypothetical protein	NA	NA	NA	NA
WP_004327095.1\|447400_447673_-	hypothetical protein	NA	NA	NA	NA
WP_008650625.1\|448055_448310_-	hypothetical protein	NA	NA	NA	NA
WP_004327094.1\|448386_448803_+	DUF3408 domain-containing protein	NA	NA	NA	NA
WP_004315818.1\|448832_449237_+	DUF3408 domain-containing protein	NA	NA	NA	NA
WP_004311277.1\|449312_450101_+	ParA family protein	NA	NA	NA	NA
WP_004327093.1\|451358_453239_+	TonB-dependent receptor plug domain-containing protein	NA	NA	NA	NA
WP_032497150.1\|453228_453426_+	hypothetical protein	NA	NA	NA	NA
WP_005821497.1\|454158_457020_+	TonB-dependent receptor	NA	NA	NA	NA
WP_008774664.1\|457105_458305_+	DUF4876 domain-containing protein	NA	NA	NA	NA
WP_008768947.1\|458328_459891_+	hypothetical protein	NA	NA	NA	NA
WP_004311267.1\|459948_462096_+	hypothetical protein	NA	NA	NA	NA
WP_004311266.1\|462102_464304_+	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_008650629.1\|464354_466499_+	hypothetical protein	NA	NA	NA	NA
WP_005651724.1\|466908_467640_+\|transposase	transposase	NA	NA	NA	NA
WP_004311263.1\|467566_471115_-	class I SAM-dependent DNA methyltransferase	A0A1B1IUC6	uncultured_Mediterranean_phage	2.5e-11	26.3
WP_004311262.1\|471310_471478_-	hypothetical protein	NA	NA	NA	NA
WP_005651718.1\|471451_471643_+	hypothetical protein	NA	NA	NA	NA
WP_032849094.1\|471776_471980_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_004311261.1\|471992_472286_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_008768946.1\|472350_473562_-\|integrase	site-specific integrase	H7BUI8	unidentified_phage	3.0e-17	27.4
WP_004311259.1\|473581_474811_-\|integrase	site-specific integrase	H7BUI8	unidentified_phage	4.9e-23	31.4
WP_080594425.1\|474927_475296_+\|integrase	integrase	NA	NA	NA	NA
479594:479608	attR	NA	NA	NA	NA

DBSCAN-SWA_2

3695730 : 3706473

unidentified_phage(83.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_005806176.1\|3695730_3696672_+	hypothetical protein	H7BUQ9	unidentified_phage	1.1e-91	56.3
WP_005806178.1\|3696674_3697475_+	hypothetical protein	H7BUR0	unidentified_phage	1.6e-62	45.4
WP_005806179.1\|3697471_3697867_+	peptidase M15	H2A0C2	Bacteroides_phage	5.9e-39	63.4
WP_032537116.1\|3697879_3698323_+	hypothetical protein	NA	NA	NA	NA
WP_005806183.1\|3698319_3698784_+	hypothetical protein	NA	NA	NA	NA
WP_080714613.1\|3698704_3702904_+	hypothetical protein	H7BUR2	unidentified_phage	5.6e-87	28.3
WP_005806187.1\|3702914_3705017_+	hypothetical protein	H7BUR3	unidentified_phage	1.1e-115	38.6
WP_065849892.1\|3705061_3705283_+	hypothetical protein	NA	NA	NA	NA
WP_032537114.1\|3705279_3706473_+	hypothetical protein	H7BUR5	unidentified_phage	6.2e-39	30.3

DBSCAN-SWA_3

5251508 : 5320820

Norovirus(20.0%)

transposase,protease,tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_122200341.1\|5251508_5252015_-\|transposase	transposase	NA	NA	NA	NA
WP_080594319.1\|5252678_5252816_+\|transposase	transposase	NA	NA	NA	NA
WP_005808376.1\|5253585_5253885_+	hypothetical protein	NA	NA	NA	NA
WP_080594320.1\|5254612_5255980_+	DUF4932 domain-containing protein	NA	NA	NA	NA
WP_050503227.1\|5256164_5257532_+	SPASM domain-containing protein	NA	NA	NA	NA
WP_005807054.1\|5257760_5259248_+\|transposase	IS1182 family transposase	NA	NA	NA	NA
WP_080594321.1\|5259244_5259469_-\|transposase	transposase	A0A218MNE7	uncultured_virus	9.2e-05	66.7
WP_005808382.1\|5259443_5260619_-\|transposase	IS66 family transposase	NA	NA	NA	NA
WP_032537009.1\|5261864_5263706_-	RagB/SusD family nutrient uptake outer membrane protein	NA	NA	NA	NA
WP_022011712.1\|5263728_5266944_-	TonB-dependent receptor	Q2PGD7	Norovirus	2.5e-50	56.2
WP_080714599.1\|5267516_5267642_+	hypothetical protein	NA	NA	NA	NA
WP_032537007.1\|5267822_5269145_-	DUF1735 domain-containing protein	NA	NA	NA	NA
WP_032537006.1\|5269171_5271058_-	RagB/SusD family nutrient uptake outer membrane protein	NA	NA	NA	NA
WP_032537005.1\|5271087_5274540_-	TonB-dependent receptor	Q2PGD7	Norovirus	1.1e-93	96.0
WP_032537004.1\|5274668_5275868_-	DUF4974 domain-containing protein	NA	NA	NA	NA
WP_005781354.1\|5275967_5276546_-	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_005808404.1\|5276806_5277883_+	chorismate synthase	A0A291AU41	Pandoravirus	5.0e-88	49.2
WP_032537003.1\|5277895_5279260_+	dipeptidase	NA	NA	NA	NA
WP_032537002.1\|5279367_5280420_-	linear amide C-N hydrolase	NA	NA	NA	NA
WP_122200537.1\|5280487_5283808_-	bifunctional proline dehydrogenase/L-glutamate gamma-semialdehyde dehydrogenase	NA	NA	NA	NA
WP_005808413.1\|5284164_5284887_-	DUF4396 domain-containing protein	NA	NA	NA	NA
WP_032537012.1\|5284976_5287127_-	DNA topoisomerase III	A0A1X9I6W8	Streptococcus_phage	9.1e-49	34.5
WP_005808417.1\|5287251_5288643_+	alpha-L-fucosidase	NA	NA	NA	NA
WP_005781369.1\|5288772_5290920_-	methylmalonyl-CoA mutase	NA	NA	NA	NA
WP_005808421.1\|5290921_5292820_-	methylmalonyl-CoA mutase small subunit	NA	NA	NA	NA
WP_080594322.1\|5293005_5293194_-	hypothetical protein	NA	NA	NA	NA
WP_080714598.1\|5293184_5293388_+	hypothetical protein	NA	NA	NA	NA
WP_032536999.1\|5293743_5295408_+	putative transporter	NA	NA	NA	NA
WP_005781380.1\|5295495_5296125_-	cytidylate kinase-like family protein	NA	NA	NA	NA
WP_005781382.1\|5296288_5297641_+	MATE family efflux transporter	NA	NA	NA	NA
WP_005781385.1\|5297682_5298252_+	Crp/Fnr family transcriptional regulator	NA	NA	NA	NA
WP_005821714.1\|5298936_5299263_+	hypothetical protein	NA	NA	NA	NA
WP_128900005.1\|5299504_5299687_-	hypothetical protein	NA	NA	NA	NA
WP_080594325.1\|5299848_5300001_+	hypothetical protein	NA	NA	NA	NA
WP_032536997.1\|5300142_5302353_-	patatin-like phospholipase domain-containing protein	A0A2H4UUE4	Bodo_saltans_virus	5.9e-19	34.7
WP_032536996.1\|5302432_5303791_-	MATE family efflux transporter	NA	NA	NA	NA
WP_005781393.1\|5303928_5305656_+\|tRNA	lysine--tRNA ligase	A0A1V0SIS0	Klosneuvirus	1.2e-96	39.7
WP_005781396.1\|5305755_5306751_+	NAD(P)H-dependent glycerol-3-phosphate dehydrogenase	NA	NA	NA	NA
WP_005781398.1\|5306776_5308114_+	glucose-6-phosphate isomerase	NA	NA	NA	NA
WP_005781399.1\|5308192_5308699_-	DUF5035 family protein	NA	NA	NA	NA
WP_005808441.1\|5308796_5309525_+	HAD family hydrolase	NA	NA	NA	NA
WP_005781403.1\|5309870_5310908_+	aspartate--ammonia ligase	A0A1C9C5F0	Heterosigma_akashiwo_virus	1.1e-55	39.5
WP_005781405.1\|5310914_5311577_+	uracil-DNA glycosylase	A0A1R3T3N6	Sphenicid_alphaherpesvirus	3.1e-48	46.3
WP_005781407.1\|5311666_5314375_-	LPS-assembly protein LptD	NA	NA	NA	NA
WP_005808444.1\|5314464_5315001_-	HDIG domain-containing protein	NA	NA	NA	NA
WP_005781411.1\|5315462_5317769_+	family 20 glycosylhydrolase	A0A2H4UUW7	Bodo_saltans_virus	2.6e-09	27.3
WP_032536995.1\|5317963_5320057_+	hypothetical protein	NA	NA	NA	NA
WP_005808448.1\|5320079_5320820_-\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr_ID: NZ_CP036546.1|WP_008645968.1|815137_815560_-|hypothetical-protein

Click the colored protein region to show detailed information

Acr_ID: NZ_CP036546.1|WP_004291533.1|1488665_1489082_+|hypothetical-protein

Click the colored protein region to show detailed information

Acr ID

Acr position

Acr size

Homology with known anti

Neighbor HTH/AcRanker

Neighbor Aca

In prophage

Protospacer in prophage

NZ_CP036546.1|WP_008645968.1|815137_815560_-|hypothetical-protein

815137_815560_-

140 aa aa

hit_Aca_id	identity	query_coverage	hit_coverage
gnl\|BL_ORD_ID\|40	0.5673758865248227	1	1.0

NZ_CP036546.1|WP_004291533.1|1488665_1489082_+|hypothetical-protein

1488665_1489082_+

138 aa aa

hit_Aca_id	identity	query_coverage	hit_coverage
gnl\|BL_ORD_ID\|40	0.5571428571428572	0.9855072463768116	0.9929078014184397

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP036546

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

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information