CRISPRimmunity

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_CP018788	Campylobacter lanienae strain NCTC 13003 chromosome, complete genome	5 crisprs	cas4,DEDDh,cas2,cas1,cas9	0	2	1	0

1. NZ_CP018788

CRISPR-Cas detection and classification

Crispr_ID: NZ_CP018788_1

• CRISPR_ID: NZ_CP018788_1
• CRISPR_location: 119100-119193
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP018788_1

Consensus_repeat	Method
GGTGGAATTTAAATAATTTTTGG	CRISPRCasFinder

spacers of NZ_CP018788_1

>1.1|119123|48|NZ_CP018788|CRISPRCasFinder
ATTGATTTGTAACTAATCTAAAAAGAAATCCTGATGTATTTTCTAAAT

CRISPR arrays and Neighbor proteins around NZ_CP018788_1

CRISPR arrays

The CRISPR arrays of NZ_CP018788_1

>merge|NZ_CP018788|1|119100-119193|CRISPRCasFinder
GGTGGAATTTAAATAATTTTTGGATTGATTTGTAACTAATCTAAAAAGAAATCCTGATGTATTTTCTAAATGGTGGAATTTAAATAGTTTTTGG

>NZ_CP018788|1|1|119100-119193|CRISPRCasFinder
GGTGGAATTTAAATAATTTTTGG	ATTGATTTGTAACTAATCTAAAAAGAAATCCTGATGTATTTTCTAAAT
GGTGGAATTTAAATAGTTTTTGG

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018788.1|WP_141081323.1|127777_128347_+|metal-dependent-hydrolase	unknown	unknown	gnl|CDD|377294
NZ_CP018788.1|WP_086301945.1|110180_111089_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187550
NZ_CP018788.1|WP_086301954.1|119249_120032_+|ABC-transporter-permease	unknown	unknown	gnl|CDD|224596
NZ_CP018788.1|WP_086301949.1|114697_115927_-|DegT/DnrJ/EryC1/StrS-family-aminotransferase	unknown	unknown	gnl|CDD|99740
NZ_CP018788.1|WP_086301948.1|113032_114082_-|GDP-L-fucose-synthase	unknown	unknown	gnl|CDD|187550
NZ_CP018788.1|WP_086251207.1|112375_112936_-|dTDP-4-dehydrorhamnose-3,5-epimerase-family-protein	unknown	unknown	gnl|CDD|224810
NZ_CP018788.1|WP_086224986.1|125450_126518_+|NAD(P)-dependent-alcohol-dehydrogenase	unknown	unknown	gnl|CDD|176186
NZ_CP018788.1|WP_086239058.1|120028_120694_+|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|213187
NZ_CP018788.1|WP_086303181.1|128685_129834_+|hypothetical-protein	unknown	unknown	gnl|CDD|225559
NZ_CP018788.1|WP_086301951.1|116621_116804_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301947.1|111325_112375_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187550
NZ_CP018788.1|WP_086301946.1|110980_111238_-|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl|CDD|187550
NZ_CP018788.1|WP_086303180.1|120705_121833_+|capsule-biosynthesis-protein	unknown	unknown	gnl|CDD|226055
NZ_CP018788.1|WP_086301950.1|116194_116449_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301952.1|116830_117922_+|hypothetical-protein	unknown	unknown	gnl|CDD|319747
NZ_CP018788.1|WP_086239276.1|114158_114698_-|dTDP-4-dehydrorhamnose-3,5-epimerase-family-protein	unknown	unknown	gnl|CDD|224810
NZ_CP018788.1|WP_086301958.1|126519_127800_+|hypothetical-protein	unknown	unknown	gnl|CDD|238538
NZ_CP018788.1|WP_086301959.1|129837_130221_+|YcfL-family-protein	unknown	unknown	gnl|CDD|176923
NZ_CP018788.1|WP_086301956.1|123122_124826_+|DUF262-domain-containing-protein	unknown	unknown	gnl|CDD|377008
NZ_CP018788.1|WP_086301955.1|121836_123030_+|hypothetical-protein	unknown	unknown	gnl|CDD|133037

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP018788.1|WP_141081323.1|127777_128347_+|metal-dependent-hydrolase	gnl|CDD|377294	pfam04307, YdjM, LexA-binding, inner membrane-associated putative hydrolase. YdjM is a family of putative LexA-binding proteins. Members are predicted to be membrane-bound metal-dependent hydrolases that may be acting as phospholipases. It is a member of the SOS network, that rescues cells from UV and other DNA-damage. Expression of YdjM is regulated by LexA.	1.63816e-13
NZ_CP018788.1|WP_086301945.1|110180_111089_-|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187550	cd05239, GDP_FS_SDR_e, GDP-fucose synthetase, extended (e) SDRs. GDP-fucose synthetase (aka 3, 5-epimerase-4-reductase) acts in the NADP-dependent synthesis of GDP-fucose from GDP-mannose. Two activities have been proposed for the same active site: epimerization and reduction. Proteins in this subgroup are extended SDRs, which have a characteristic active site tetrad and an NADP-binding motif, [AT]GXXGXXG, that is a close match to the archetypical form. 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.	2.4357e-87
NZ_CP018788.1|WP_086301954.1|119249_120032_+|ABC-transporter-permease	gnl|CDD|224596	COG1682, TagG, ABC-type polysaccharide/polyol phosphate export systems, permease component [Carbohydrate transport and metabolism / Cell envelope biogenesis, outer membrane].	3.80762e-34
NZ_CP018788.1|WP_086301949.1|114697_115927_-|DegT/DnrJ/EryC1/StrS-family-aminotransferase	gnl|CDD|99740	cd00616, AHBA_syn, 3-amino-5-hydroxybenzoic acid synthase family (AHBA_syn). AHBA_syn family belongs to pyridoxal phosphate (PLP)-dependent aspartate aminotransferase superfamily (fold I). The members of this CD are involved in various biosynthetic pathways for secondary metabolites. Some well studied proteins in this CD are AHBA_synthase, protein product of pleiotropic regulatory gene degT, Arnb aminotransferase and pilin glycosylation protein. The prototype of this family, the AHBA_synthase, is a dimeric PLP dependent enzyme. AHBA_syn is the terminal enzyme of 3-amino-5-hydroxybenzoic acid (AHBA) formation which is involved in the biosynthesis of ansamycin antibiotics, including rifamycin B. Some members of this CD are involved in 4-amino-6-deoxy-monosaccharide D-perosamine synthesis. Perosamine is an important element in the glycosylation of several cell products, such as antibiotics and lipopolysaccharides of gram-positive and gram-negative bacteria. The pilin glycosylation protein encoded by gene pglA, is a galactosyltransferase involved in pilin glycosylation. Additionally, this CD consists of ArnB (PmrH) aminotransferase, a 4-amino-4-deoxy-L-arabinose lipopolysaccharide-modifying enzyme. This CD also consists of several predicted pyridoxal phosphate-dependent enzymes apparently involved in regulation of cell wall biogenesis. The catalytic lysine which is present in all characterized PLP dependent enzymes is replaced by histidine in some members of this CD.	8.72365e-108
NZ_CP018788.1|WP_086239276.1|114158_114698_-|dTDP-4-dehydrorhamnose-3,5-epimerase-family-protein	gnl|CDD|224810	COG1898, RfbC, dTDP-4-dehydrorhamnose 3,5-epimerase and related enzymes [Cell envelope biogenesis, outer membrane].	1.48681e-52
NZ_CP018788.1|WP_086303180.1|120705_121833_+|capsule-biosynthesis-protein	gnl|CDD|226055	COG3524, KpsE, Capsule polysaccharide export protein [Cell envelope biogenesis, outer membrane].	8.49084e-109
NZ_CP018788.1|WP_086224986.1|125450_126518_+|NAD(P)-dependent-alcohol-dehydrogenase	gnl|CDD|176186	cd05283, CAD1, Cinnamyl alcohol dehydrogenases (CAD). Cinnamyl alcohol dehydrogenases (CAD), members of the medium chain dehydrogenase/reductase family, reduce cinnamaldehydes to cinnamyl alcohols in the last step of monolignal metabolism in plant cells walls. CAD binds 2 zinc ions and is NADPH- dependent. CAD family members are also found in non-plant species, e.g. in yeast where they have an aldehyde reductase activity. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P) binding-Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability. ADH-like proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and generally have 2 tightly bound zinc atoms per subunit. The active site zinc is coordinated by a histidine, two cysteines, and a water molecule. The second zinc seems to play a structural role, affects subunit interactions, and is typically coordinated by 4 cysteines.	8.03581e-162
NZ_CP018788.1|WP_086239058.1|120028_120694_+|ABC-transporter-ATP-binding-protein	gnl|CDD|213187	cd03220, ABC_KpsT_Wzt, ATP-binding cassette component of polysaccharide transport system. The KpsT/Wzt ABC transporter subfamily is involved in extracellular polysaccharide export. Among the variety of membrane-linked or extracellular polysaccharides excreted by bacteria, only capsular polysaccharides, lipopolysaccharides, and teichoic acids have been shown to be exported by ABC transporters. A typical system is made of a conserved integral membrane and an ABC. In addition to these proteins, capsular polysaccharide exporter systems require two 'accessory' proteins to perform their function: a periplasmic (E.coli) or a lipid-anchored outer membrane protein called OMA (Neisseria meningitidis and Haemophilus influenza) and a cytoplasmic membrane protein MPA2.	2.47899e-86
NZ_CP018788.1|WP_086303181.1|128685_129834_+|hypothetical-protein	gnl|CDD|225559	COG3014, COG3014, Uncharacterized protein conserved in bacteria [Function unknown].	2.10451e-98
NZ_CP018788.1|WP_086301947.1|111325_112375_-|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187550	cd05239, GDP_FS_SDR_e, GDP-fucose synthetase, extended (e) SDRs. GDP-fucose synthetase (aka 3, 5-epimerase-4-reductase) acts in the NADP-dependent synthesis of GDP-fucose from GDP-mannose. Two activities have been proposed for the same active site: epimerization and reduction. Proteins in this subgroup are extended SDRs, which have a characteristic active site tetrad and an NADP-binding motif, [AT]GXXGXXG, that is a close match to the archetypical form. 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.	1.16593e-116
NZ_CP018788.1|WP_086301946.1|110980_111238_-|NAD-dependent-epimerase/dehydratase-family-protein	gnl|CDD|187550	cd05239, GDP_FS_SDR_e, GDP-fucose synthetase, extended (e) SDRs. GDP-fucose synthetase (aka 3, 5-epimerase-4-reductase) acts in the NADP-dependent synthesis of GDP-fucose from GDP-mannose. Two activities have been proposed for the same active site: epimerization and reduction. Proteins in this subgroup are extended SDRs, which have a characteristic active site tetrad and an NADP-binding motif, [AT]GXXGXXG, that is a close match to the archetypical form. 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.	1.0962e-16
NZ_CP018788.1|WP_086251207.1|112375_112936_-|dTDP-4-dehydrorhamnose-3,5-epimerase-family-protein	gnl|CDD|224810	COG1898, RfbC, dTDP-4-dehydrorhamnose 3,5-epimerase and related enzymes [Cell envelope biogenesis, outer membrane].	1.16663e-45
NZ_CP018788.1|WP_086301952.1|116830_117922_+|hypothetical-protein	gnl|CDD|319747	cd16439, beta_Kdo_transferase_KpsC_2, beta-3-deoxy-D-manno-oct-2-ulosonic acid (Kdo)-transferase KpsC, repeat 2. KpsC is a beta-3-deoxy-D-manno-oct-2-ulosonic acid (Kdo)-transferase. It is part of the ATP-binding cassette transporter dependent capsular polysaccharides (CPSs) synthesis pathway, one of two CPS synthesis pathways present in Escherichia coli. The poly-Kdo linker is thought to be the common feature of CPSs synthesized via this pathway. CPSs are high-molecular-mass cell-surface polysaccharides that are important virulence factors for many pathogenic bacteria. KpsC contains a domain duplication.	1.02149e-149
NZ_CP018788.1|WP_086301948.1|113032_114082_-|GDP-L-fucose-synthase	gnl|CDD|187550	cd05239, GDP_FS_SDR_e, GDP-fucose synthetase, extended (e) SDRs. GDP-fucose synthetase (aka 3, 5-epimerase-4-reductase) acts in the NADP-dependent synthesis of GDP-fucose from GDP-mannose. Two activities have been proposed for the same active site: epimerization and reduction. Proteins in this subgroup are extended SDRs, which have a characteristic active site tetrad and an NADP-binding motif, [AT]GXXGXXG, that is a close match to the archetypical form. 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.	1.29564e-140
NZ_CP018788.1|WP_086301958.1|126519_127800_+|hypothetical-protein	gnl|CDD|238538	cd01118, ArsB_permease, Anion permease ArsB. These permeases have been shown to export arsenate and antimonite in eubacteria and archaea. A typical ArsB permease contains 8-13 transmembrane helices and can function either independently as a chemiosmotic transporter or as a channel-forming subunit of an ATP-driven anion pump (ArsAB). The ArsAB complex is similar in many ways to ATP-binding cassette transporters, which have two groups of six transmembrane-spanning helical segments and two nucleotide-binding domains. The ArsB proteins belong to the ArsB/NhaD superfamily of permeases that translocate sodium, arsenate, sulfate, and organic anions across biological membranes in all three kingdoms of life.	4.53969e-91
NZ_CP018788.1|WP_086301959.1|129837_130221_+|YcfL-family-protein	gnl|CDD|176923	cd09030, DUF1425, Putative periplasmic lipoprotein. This bacterial family of proteins contains members described as putative lipoproteins, some are also known as YcfL. The function of this family is unknown. Family members have also been annotated as predicted periplasmic lipoproteins (COG5633), and appear to contain an N-terminal membrane lipoprotein lipid attachment side (pfam08139), which is not included in this alignment model.	5.3179e-16
NZ_CP018788.1|WP_086301956.1|123122_124826_+|DUF262-domain-containing-protein	gnl|CDD|377008	pfam03235, DUF262, Protein of unknown function DUF262.	5.2458e-25
NZ_CP018788.1|WP_086301955.1|121836_123030_+|hypothetical-protein	gnl|CDD|133037	cd04194, GT8_A4GalT_like, A4GalT_like proteins catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The members of this family of glycosyltransferases catalyze the addition of galactose or glucose residues to the lipooligosaccharide (LOS) or lipopolysaccharide (LPS) of the bacterial cell surface. The enzymes exhibit broad substrate specificities. The known functions found in this family include: Alpha-1,4-galactosyltransferase, LOS-alpha-1,3-D-galactosyltransferase, UDP-glucose:(galactosyl) LPS alpha1,2-glucosyltransferase, UDP-galactose: (glucosyl) LPS alpha1,2-galactosyltransferase, and UDP-glucose:(glucosyl) LPS alpha1,2-glucosyltransferase. Alpha-1,4-galactosyltransferase from N. meningitidis adds an alpha-galactose from UDP-Gal (the donor) to a terminal lactose (the acceptor) of the LOS structure of outer membrane. LOSs are virulence factors that enable the organism to evade the immune system of host cells. In E. coli, the three alpha-1,2-glycosyltransferases, that are involved in the synthesis of the outer core region of the LPS, are all members of this family. The three enzymes share 40 % of sequence identity, but have different sugar donor or acceptor specificities, representing the structural diversity of LPS.	0.00731913

Protein sequences

>NZ_CP018788.1|WP_086301952.1|116830_117922_+|hypothetical-protein
MENNKKFLFGFSIWKRKFMVPFLGGNLNFISTFSKDPLLLALKKGLNPSSLVYIWGKKEYPKLQKWCDENGVSIIRVEDGFIRSIGLGSDLTRPYSLVFDDVGIYFDTTKPSRLENILNYHKFSAYELEEAIKLKQNLINSKISKYNDDKDGIITPKNSKKIALVIGQVEDDASVKIGADGMKNIELIKQARSNSPKAHIIYKPHPDVLSGNRIGQVDESEALKYCDEIVTGVSMPVLLDIADEIHTMTSTSGLEAILRGKRVICYGRPFWAGWGLSDDKKPLPRRCRNLNIDELIAGAYIIYPRYIYPVSLETCGASDLVLALQGQKQELQKPINAVLHKIWSLYARIGQKILYVVLFVVKR
>NZ_CP018788.1|WP_086301951.1|116621_116804_+|hypothetical-protein
MLSFIVPVFYKDYNSFIYNRAVELINKFSNHPKIEIVIADASKNPNLIAHASNIKIITQG
>NZ_CP018788.1|WP_086301950.1|116194_116449_-|hypothetical-protein
MFKFKSTILMLFLSATFALANGYFIGFSGGLNHSLVDDDNYDLKSDNNLLLSPKFGYQINNTHRYSISYEHGGKSSGSKAIISN
>NZ_CP018788.1|WP_086301949.1|114697_115927_-|DegT/DnrJ/EryC1/StrS-family-aminotransferase
MQGYSLASSTWDEKELNAINEVIKSDIFTMGKKVAEFEKDFAKFVGSKYAVMTSSGSTANLIATAALFYTKNNKLKRGDEVIVPAVSWSTTYYPLHQYGLKLKFVDVDLHTLNYDLEALKNAISNKTKMIMCVNLLGNPNDFDAIKAMICDKNIILLEDNCESMGAEYKGKQAGTFGIMGTFSTFYSHHMATMEGGFVVTDDEDLYHILLCLRAHGWTRNLPKENLVAPKSDDWFSESFRFVLPGYNVRPVEMSGAIGIEQLKKLPNFLKHRRENAKLFQKYFANHPDFIIQQEIGSSSWFGFSLIIKPTSKLKRADIIKLLEANNIEYRPIATGDFTQNEVIKYFDYEIFGELKNAKYLQENGFFVGNHQIDISNQINLLNSVIVGGGRPLNNKFQISIAYLSELKVA
>NZ_CP018788.1|WP_086239276.1|114158_114698_-|dTDP-4-dehydrorhamnose-3,5-epimerase-family-protein
MAIEFDIQESKKLKGVYIITPNKFRDLRGEIWSAFTSEAIDKLLPNNLRFIHDKFIHSKHNVIRGIHGDKNTYKLATCVYGQIHQVVVDCNENSPTYLQYEEFVIDADNQKMILVPAGFGNAHYVSSQSAVYYYKCAYIGKYTDADEQFTYAWNDPRIGIEWPTTNPILSERDMLITQN
>NZ_CP018788.1|WP_086301948.1|113032_114082_-|GDP-L-fucose-synthase
MEKNSKIYIAGHRGLVGSAILRKLQNDGYLNLIYKTHDELDLTNQQEVKKFFEIEKPEFVILCAAKAGGIGANSKYRADFIYQNLMIECNVIHQAYLNGVKKLLFIASTTVYPKNATLPTNESWMLKGDLDYANKPYALSKIAGCLMCESYNLQYNTNFISITPTNLYGNNDKFDLEKSHVVPGILRKMHLAKLLNENRYDELLNDLNMPNLDEALVYLNKFGINENSVEIWGDGTPTREFLHSDDLAEAALFIMKKINFKDLIDNSQEIQNTHLNIGPNENITIKELATLIKEIVGFKGDLTFNANRPNGAMNKLTDCSKIHSLGWKHKINLEEGVKMLYQWYKNGGV
>NZ_CP018788.1|WP_086251207.1|112375_112936_-|dTDP-4-dehydrorhamnose-3,5-epimerase-family-protein
MAIEFDIQESKKLKGVYIITPSKFKDLRGEIWSAYSSEAILKLLPNGLNFVLDKFTLSKPNVLRGIHGDHKSWKLVTCVTGEIHQVVVDCQKESPTYLQYEKFIINSDNQKLILIPPRFGNAQYVSSKCDSMYYYKWAYEGEYVDASDQFTFAWNDPRIAIDWPTNTPILSNRDIEAMTQDHTKGF
>NZ_CP018788.1|WP_086301947.1|111325_112375_-|NAD-dependent-epimerase/dehydratase-family-protein
MDKNSKIYIAGHNGTAGTALVDNLRARGYNNLILRTRQELDLTNQEAVADLFKNEKPEYVFLCAVLPCGAANVAQRADFIYVNLMIQNNIIHQSYLHGVKKLICYGSGYMYPYHAKNPLKEEYMMQSVLEYNAYTMGIAKIAGAAMCEAYNIQYGTNFLCLALNNLYGTRANFDFGKSRVLPALLCKFHLAKMLEDDNFEGVLADLNMNEKEATEILNNYGIAKDSVEIWGTGKVKREFIHSDDLADASIFTMENINFSDLAKGKNPQNTHINIGSGVAYSIAEVVDMIKGIVGFNGQLYFNTSRPDSTMDRLMDVSKINSLGWKHKIELEEGIKMMYQWYKTSIKGRG
>NZ_CP018788.1|WP_086301946.1|110980_111238_-|NAD-dependent-epimerase/dehydratase-family-protein
MDKNSKIYISGHRGLVGSAIIEELQKQGYANLIYKTHNELDLINQKAVNEFLNKKNLIMYFSVLLLRVDLSNKRNIRLNFYTIIS
>NZ_CP018788.1|WP_086301945.1|110180_111089_-|NAD-dependent-epimerase/dehydratase-family-protein
MFEQEKPDYVFFSAAFAGGFIKQKKYPAEFLYNNIMMQNNVIWAAANNGVKKLIYLASACVFPKDAPLPLEERYMLEGAFQPNNESYAIGKVAGIKLCEYLNLEKGKNFLCVAPTSIYGENDNFNIEDSHVQAGIFRKIYLAKMRNENNINALCKDLNLNQKEALEFCDKHGIFDNYIKMIGTGAAAREFANSRDLAGFCIYLAQNIDFKDLCEYDENGNLISSFVNFTDGEPVSIKELSFLIVKLMDYKGELIFEKELSRNDGTLRKTMSRKKINKLGYQNKISLKNGLKKMIEMYGVWSR
>NZ_CP018788.1|WP_086301954.1|119249_120032_+|ABC-transporter-permease
MLNVIRALFFRELKTRFGKNRHLGYFWVVGEPLMQILVITTLVTLIREYITNLSIPGGTPVFMFLACGIIPFFMFRNIVTQLMGGIAGNLTLFFYKPVRPIHVFLARTLLEFYMYSLIFFCVMVLAGWIMGYDVLPRDFLAMFVSLALMVLSGFSLGVIFAIITHFMEPLKIVLTYFTAALYMLSCVIFPIWIIPSNILQYMLYNPMLHICESIKYYYFDGYPLADGVNLAYPLVFNVVLLFIGFWFYYYKRRELVASRP
>NZ_CP018788.1|WP_086239058.1|120028_120694_+|ABC-transporter-ATP-binding-protein
MIKLDNLTKFYPLSNGDKHFVFREFTFTFPDDCSIGLIGRNGAGKSTLMRLLSGADIPNAGRVITDKKISWPVGLAGGFQSSLSARDNVKFVARVYGYRGEALEEKVRYIEEFAEIGKYFDEPMNTYSSGMRSRIGFGLSMAFDFDYYLIDEAGAVGDAKFKKKSDAIYKEKLSNSKVIMVSHNMAEIKQWCDKIILVNSGMTTVYDDVDEGIEMYKRICS
>NZ_CP018788.1|WP_086303180.1|120705_121833_+|capsule-biosynthesis-protein
MILRSIKDLKQHKERLNRLDSFKTVIYIMIVVIFYYAFIAADRYVSNVSLSVKSTDGGSPISLSGIESLVGVASSSTEDIKLLQEYIKSFDMLQKLDEKINLRSLYEKQKIDLFFRIYSSTSKESYLKYYRDRIHILFDDTTGLLNVAVEGFSPEDARNISAAILEESERFINEISHNIAREQLRFAQGELESAKQKYKDAKNELLAFQNEYGVFDPQSLAKTKAGFITEIELQISKKETELNTMRSYLNDNAPEIAALKAELRAHKEQLEKEKRKVASNASQDKLNDVVAQFEALYLNLSFAEDVYKTAITAVETTRIEIGRKAKQVVVIQSPYVPDSAAYPNKMYNIITIFVILTLIFGVVRLVRAIIDEHRY
>NZ_CP018788.1|WP_086301955.1|121836_123030_+|hypothetical-protein
MKKPYKNGILLAATSNSAFAIGTMVANIAEVMGGEVDIFYIVHDGFTQSELEAFARVAGGAKVKFISFTKDDFAKRLKPHTNNQNILNSPFFSRWTHMAYGMFEPLLLLDECECIVYLDFDILLLKGVGELFRLKGYHFSAHRGKSLLNPTLRDYNGEFKDCRVYRSGIVAYYDTIPNPKECYNQIYNYSAKYGANDQGVLSLLILDNKFKVKNLGYEYTSSTFWRKSIGASIIHAWGRDGRFWNNELVYQFWGEIWDKYYQKWLKCGGSEYKGGFICKANYAIERIRYHLAYKLGYAMIENHTTIFGKIKLPFILLAIALKHRGQKIEYLQIIQTKPNLKVPPIEHYEDYKPALAEKQSAPYRLGQALIKATKTWYKGGLIKLYFEINEIKRDKKG
>NZ_CP018788.1|WP_086301956.1|123122_124826_+|DUF262-domain-containing-protein
MSKLNIDQKKIKQLFEDKRSDFLIPDYQRPYAWGEDECQTLWKDIFDFAFPDKKPENFNSDEEYFLGPIVTFENNKKLEVIDGQQRLTTLMLLLRVFYKRLEKMEDENSMRTKQNLAQCIWKSDEFGNENKEKLKIDSQVALDEHKNEFLEILKTGDAKDFKSQYAINFRYFEKEVDEFLKEYPNYFAYLPTRILNNCILLPIEADNEKTALRIFSTLNDRGKPLADADIFKAQFYKFYVAKNQKDEFIEKWKNLEILCKEVFSKKDNTSTDEIFNRYMYYQRALKGNKNSTTEGLRDFYEKDSYALLKSDRTFEDLQNLGSFWQAISIQDKNYFDENTLRWLFILNYAPNIMWANITSVYFMKNKDEQNKLDNIKFAKFLEKITAFIFAYSFIYPSVSQLRIPIYSVMVDIINDKEMDFSKFLFEKENLKTFIQTQKFSNNNSITRSMLTWWFLKDSTQKTPGLTEQFQIEHIYAKERAKRENFSGNEIEFIGNKVLLERKINIRASDFSFADKEKHYKKSQNNELNSIHKNYSEFSKTEIIERNNNIINDFISFVEKNNLIKTTS
>NZ_CP018788.1|WP_086224986.1|125450_126518_+|NAD(P)-dependent-alcohol-dehydrogenase
MNNIFTIPATGYAMLSKDSKFTPIEFTRHSVGDNDILIEILYSGICHSDIHTAKDEWGGTSYPCIPGHEIAGQVIAVGKNVTKFKIGDYAGVGCMVNSCGECEACKASQEQFCQQGKTVYTYNCPDFFHGGKITFGGYSSNIVVSQNFAIKVRANAPLDKVAPLLCAGITTYSPLKFSKIKAGDKVGVAGFGGLGMMALKYAVKMGAQVSVFARNENKKADALALGATSFYTNTDKNIVNERFDLIISTIPTSYDVIAYIDLLKFGGELAIVGLPPYKEAPSVSIIDLVHKAGKKIYGSLIGGIKETQEMLDFSLENEIYPETILITPNQIDEAYEKLTNGSGQFRYVIDMKASN
>NZ_CP018788.1|WP_086301958.1|126519_127800_+|hypothetical-protein
MAFAIFAISMALIYTRPFGLPVWASAVAGAIAAMMFGVVSVSSAFGVLAMVWDSTLVLVGLIIIAMAFEQMGFFDALAGRIIGKFAKGSGGIYRIATLKFFALMMGLGLFVATFLANDGAILVLTPLVFALFSNTKDELSITTPLVAFLLFFGFLSDFGSNALIISNLTNIITAKLFNLSFKEYFEAMVLAQIFAFIAACGLFWLVLARRLPAVLEFKLPARRIGSGRFLACLFLLILLPIGSMIFEEMELPISLFILLVALISIMMQDSGKFALFKRAPFGVVVFSVGLFVMVYGVGMAGILEFLRQNIQMLAGLDRFSSLLGIALGSSIGSALINNLPMVMLGDLALRDFGADMGLIYAHLLGCNIGSKLTPIGSLATLLWLANLKLRGVKISLLDYFKFTFIFSLGVLFAAVLGLWIGESFDI
>NZ_CP018788.1|WP_141081323.1|127777_128347_+|metal-dependent-hydrolase
MERVLTFRTHLAIGALGAMGFVGAVDLSGVANLDKTQTAYVVGLILFGSVLPDIDEPRSFISRKFPLISQITATFFKHRGPTHFLFIPVLLFVAWAIFGQIAWGALGFGMIMHHVGDMLTPSGIQGYFYPFKKRFVARILPKKIAVKTGSTVEMALVLPAILAVDGFLGAKILGFDIDMGRILGILNLI
>NZ_CP018788.1|WP_086303181.1|128685_129834_+|hypothetical-protein
MARVCQEFALSNELLDIAEDKYKYDVDLESTGNKIARNLVGILLNDTFSDYDGNLYERIMVNLYKGLNFMSLNDFENARVEFNRALIRQDMAKEYFAPQIQAAKEELEKQKSDPNYKKNLKNTKLVYDEYSRLFKEFKTSENFINPYATYAASVFFYLDKDYKNSADKFREIAIANPKNKAISAINKRLQTRAKNVKSKGKKYIFLAYEDGLGTIKNEFAINIPYIISDGVATLSLSLPMLKKRDFSYKDISINGVKATQISNFDNIFATEFKIELPWIITKSILSGTIKSATSAVVADKFGGVASLATTFLLSATNKADIRVWQTLPKIASIAMVENKGSYTIKDSSGKIIASDKIDKSKDALIWLRSSNKDMVKSIIIQR
>NZ_CP018788.1|WP_086301959.1|129837_130221_+|YcfL-family-protein
MKKLAMFLVCAMLFGCAGNSDIVLGDSGYNSNLVSLEAIDRDIVQGINHRFNDLGLLEFQVILKSNSEMDVAYKVVWLDESGFELRNSIDESYKILRLNANRQISINKLAQDKRAKSFKIYLTTKGL

Crispr_ID: NZ_CP018788_2

• CRISPR_ID: NZ_CP018788_2
• CRISPR_location: 181838-181940
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_CP018788_2

Consensus_repeat	Method
CCAGCTAGATATATCTGAGTTAAAATTT	CRISPRCasFinder

spacers of NZ_CP018788_2

>2.1|181866|47|NZ_CP018788|CRISPRCasFinder
ACAGCACCAGCGAACATATAGTTCATATTGGTTACATTAGATACATC

CRISPR arrays and Neighbor proteins around NZ_CP018788_2

CRISPR arrays

The CRISPR arrays of NZ_CP018788_2

>merge|NZ_CP018788|2|181838-181940|CRISPRCasFinder
CCAGCTAGATATATCTGAGTTAAAATTTACAGCACCAGCGAACATATAGTTCATATTGGTTACATTAGATACATCCCAGTTAGATATATCTGAGTTAAAATTT

>NZ_CP018788|2|2|181838-181940|CRISPRCasFinder
CCAGCTAGATATATCTGAGTTAAAATTT	ACAGCACCAGCGAACATATAGTTCATATTGGTTACATTAGATACATC
CCAGTTAGATATATCTGAGTTAAAATTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018788.1|WP_086301988.1|178852_179980_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301995.1|195042_195273_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301992.1|189458_191168_-|dynamin-family-protein	unknown	unknown	gnl|CDD|366045
NZ_CP018788.1|WP_086229311.1|187247_189446_-|dynamin-family-protein	unknown	unknown	gnl|CDD|206739
NZ_CP018788.1|WP_086301985.1|171189_173046_+|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552	unknown	unknown	gnl|CDD|225840
NZ_CP018788.1|WP_086303185.1|170660_171131_+|cytochrome-c-nitrite-reductase-small-subunit	unknown	unknown	gnl|CDD|274453
NZ_CP018788.1|WP_086235117.1|169138_170455_+|MATE-family-efflux-transporter	unknown	unknown	gnl|CDD|240539
NZ_CP018788.1|WP_086301993.1|191412_191877_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301991.1|185091_187245_-|BspA-family-leucine-rich-repeat-surface-protein	unknown	unknown	gnl|CDD|184118
NZ_CP018788.1|WP_180383468.1|192461_192635_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_115633444.1|193320_193578_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301989.1|180019_181432_-|dynamin-family-protein	unknown	unknown	gnl|CDD|366045
NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_CP018788.1|WP_086301986.1|173256_174237_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270260
NZ_CP018788.1|WP_086301994.1|194327_194942_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_180381652.1|192261_192426_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_181892508.1|174552_177342_+|flagellar-hook-protein-FlgE	unknown	unknown	gnl|CDD|236263
NZ_CP018788.1|WP_086301984.1|167040_168822_-|phosphoethanolamine-transferase	unknown	unknown	gnl|CDD|293741
NZ_CP018788.1|WP_086303187.1|183486_184527_-|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|236815
NZ_CP018788.1|WP_086224945.1|178659_178839_-|hypothetical-protein	unknown	unknown	unknown

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	5.7e-32	106.1	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP018788.1|WP_086301992.1|189458_191168_-|dynamin-family-protein	gnl|CDD|366045	pfam00350, Dynamin_N, Dynamin family.	3.53266e-15
NZ_CP018788.1|WP_086229311.1|187247_189446_-|dynamin-family-protein	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	3.19345e-11
NZ_CP018788.1|WP_086301985.1|171189_173046_+|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552	gnl|CDD|225840	COG3303, NrfA, Formate-dependent nitrite reductase, periplasmic cytochrome c552 subunit [Inorganic ion transport and metabolism].	2.16953e-155
NZ_CP018788.1|WP_086303185.1|170660_171131_+|cytochrome-c-nitrite-reductase-small-subunit	gnl|CDD|274453	TIGR03153, cytochr_NrfH, cytochrome c nitrite reductase, small subunit. Members of this protein family are NrfH, a tetraheme cytochrome c. NrfH is the cytochrome c nitrite reductase small subunit, and forms a heterodimer with NrfA, the catalytic subunit. While NrfA can act as a monomer, NrfH can bind to and anchor NrfA in the membrane and enables electron transfer to NrfA from quinones. [Energy metabolism, Electron transport].	1.33363e-53
NZ_CP018788.1|WP_086235117.1|169138_170455_+|MATE-family-efflux-transporter	gnl|CDD|240539	cd13134, MATE_like_8, Uncharacterized subfamily of the multidrug and toxic compound extrusion (MATE) proteins. The integral membrane proteins from the MATE family are involved in exporting metabolites across the cell membrane and are responsible for multidrug resistance (MDR) in many bacteria and animals. A number of family members are involved in the synthesis of peptidoglycan components in bacteria.	4.55188e-133
NZ_CP018788.1|WP_086301991.1|185091_187245_-|BspA-family-leucine-rich-repeat-surface-protein	gnl|CDD|184118	PRK13531, PRK13531, regulatory ATPase RavA; Provisional.	1.79415e-79
NZ_CP018788.1|WP_086301989.1|180019_181432_-|dynamin-family-protein	gnl|CDD|366045	pfam00350, Dynamin_N, Dynamin family.	3.52866e-11
NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	3.79289e-28
NZ_CP018788.1|WP_086301986.1|173256_174237_+|extracellular-solute-binding-protein	gnl|CDD|270260	cd13542, PBP2_FutA1_ilke, Substrate binding domain of ferric iron-binding protein, a member of the type 2 periplasmic binding fold superfamily. FutA1 is the periplasmic component of an ABC-type iron transporter and serves as the primary receptor in Synerchosystis species. The periplasmic iron binding protein plays an essential role in the iron uptake pathway of Gram-negative pathogenic bacteria and is critical for survival of these pathogens within the host. After binding iron with high affinity, FutA1 interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The iron- and thiamine-binding proteins belong to the PBPI2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	4.45307e-116
NZ_CP018788.1|WP_181892508.1|174552_177342_+|flagellar-hook-protein-FlgE	gnl|CDD|236263	PRK08425, flgE, flagellar hook protein FlgE; Validated.	7.90715e-166
NZ_CP018788.1|WP_086301984.1|167040_168822_-|phosphoethanolamine-transferase	gnl|CDD|293741	cd16017, LptA, Lipooligosaccharide Phosphoethanolamine Transferase A (LptA) or Lipid A Phosphoethanolamine Transferase. Lipooligosaccharide Phosphoethanolamine Transferase A (LptA) or Lipid A Phosphoethanolamine Transferase catalyzes the modification of the lipid A headgroups by phosphoethanolamine (PEA) or 4-amino-arabinose residues. Lipopolysaccharides, also called endotoxins, protect bacterial pathogens from antimicrobial peptides and have roles in virulence. The PEA modified lipid A increases resistance to the cationic cyclic polypeptide antibiotic, polymyxin. Lipid A PEA transferases usually consist of a transmembrane domain anchoring the enzyme to the periplasmic face of the cytoplasmic membrane.	1.17689e-72
NZ_CP018788.1|WP_086303187.1|183486_184527_-|VWA-domain-containing-protein	gnl|CDD|236815	PRK10997, yieM, ATPase RavA stimulator ViaA.	7.68634e-47

Protein sequences

>NZ_CP018788.1|WP_086301989.1|180019_181432_-|dynamin-family-protein
MQELQIINEILSAKPNNQTLSSFNKYLNNFYDITKKIAVENERDLVLNLKAIESEMAIIAAYAELFSKHVIAVGGGFSAGKSAFVNSFLKSKDIQLPISIDPTTAIPSYVMSSDKDQIIGISKNNGVANLGKIAPDILSRLTHNADNRLNFSFNLKDILPFLVVSSEFNDPKYQNICFIDTPGYNPNSDGNRAQDFNTAKEFLANSSSLLWLISCDASGGNITESDIKFLNSIGLENKKLYFIITKADKRPKSDLDEVLENLKDTLDMEGIEYEGISLYSSTDIEEYGYHKLSLFDFILSQINNKHSKSQENVMTNLIRVYQSYEKALVKKQDDNDRIFSVLHSITIEMAYIDDEENEEHTFKVDQYAKNLKSIFSSTYSDECKKLLKELTKAFKELKSSIDAIFGAVYDWDADANKITTKDIEQLSDLRKTIDLDGDDDLPKKPKGSTKAIQEANSAVQKTGFFNFEVK
>NZ_CP018788.1|WP_086301988.1|178852_179980_-|hypothetical-protein
MHNLLILYNPRYNSDLIKEHLELLKECGKVAFGKVRVKNNNMPHPFKGELEKIYSDTNPDSFTQLFITDYSNLYVAKVVKISSDDHTPIAPKYYQEQNLLVESWFVITDMREIYRNEFESVRDYFLSRITLPLRDNHTYALYGNNYVYPLIIDQDQNYFEDETLHHTDIYKTKKYLKTKKTLSRYCFGTNIDKLMSDTIDAVVLAEIEYIQNQKNMSNDFSSILVKYSKSVEREFYSLFKALFAYLCYNNSGLLTIRYDVQGIKYQLKDIFTHKPNLGSYGYLMKQSEISSTFENLVPNDIKNGFYYKILNFMHILKDIRNENIHGKNATIKETQKIRNAILGIGQESILITCLELKSKLNALYKESKIDRSKQI
>NZ_CP018788.1|WP_086224945.1|178659_178839_-|hypothetical-protein
MNGFVPHIQTLKCPKCGKKKVITAGCVINFYSCPKCNTIMIPSSGNFIDKLIGKLKGGR
>NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein
MNSNGSNGENMIRRLMIMLKMLYLGQGLNPSELCSEFNLSLRTLQRDIARLKEYCAVDIQKGKDGKYYISRTEYEDGLLSFGDIKTFAKRSGVADLYPKLDTPMIADILSTTISKSLIVSSEPKQDSKELKDLFELLSDAILEHCVISFYYNDSQRTIKPYKLINTAGVWYLLGDEKAKLKHFTLSKIKSYKPLDQHFTPSNTFLKRIESNNLKWFSTSLKNAKILVLPKAREYFERKQVFKSYKLIKDDENGILLDVEFAFDDELLNIIKAWIPYIKIIEPQELDTKLKDILKSYINDEPISNLA
>NZ_CP018788.1|WP_181892508.1|174552_177342_+|flagellar-hook-protein-FlgE
MMGALWSGVTGLQAHQVAMDVEGNNIANVNTVGFKYSRASFADLFSQTQKVATAPQGDLGGKNSMQIGLGSTVNTVTKIFKQGTIQTTDKQSDMAIQGDGFFVVSADGGKTYMYTRNGDFSLDSKGNFVDRNGYVVQGWMRNEDTGTIDPTSPLSNIIIEPGMAMEANPTSELAIIANLNSGSNIGAKNSPIYTLDHYNDFLDANGNGLWEDGETKNPNDLSNNTYYINSNKEVAVKEAGVDLGVVFNGSGEGLNLREGQGIWVSYADAKATFGELPNNAGQGTNKYKLHISINGIEIPATELTKMDEVVKKINDYTPQTGVIATLNGDKGIQLTNTNNQGTTDATKNIKIKKLEDDTTSIRTTSVITAYKYTYSSGAGKTADHNYNDGAARVVKTTEDLRRAMQTDAREYVNYSGSNVSNAVNGATYITNKILGIIDAAGNVQTAKQNVRNQIQRALQDGQATFNGFKNNGAITEPISEAAVGVMVSILNSSDQIMQNQQITTINDLKEAIRELVTNDKLAEFASREWDSPLDADGDGNFNNNTANDLPAPEADGSHANGTYRDINLNDGVQVTVNEKGQFVFRNPAGDASYGQNDGHTIVNQNQQGGTKVEDSADAYTDTNGQKKTPANADTYTNDYAMQIAVSGYSNAAQNVNENSALADVFKALGGSLATGTGEKVSSNLTMSSHAATTEIYDSLGSKHEIKFEWRKVSYSPENGTEWSVLIQVPEPGVLNTDGSGFSNVVSGSARFNNDGTLLGFTPTTLSFTANNGSAPGQGIELNFGKIGDSNGLRSNDNPSATDNIIQDGYTAGNLVGTRIDEAGTIIGSFSNGRSFGLAQVSLAVFSNNEGLESRSGNIFSQTANSGDPIFGAAGTSRRGTITASALEMSNVDLSRALTQLIVVQRGYQANSKTITTSDQMLTSLLQIKQ
>NZ_CP018788.1|WP_086301986.1|173256_174237_+|extracellular-solute-binding-protein
MKKLLLTAAFACMALANEINLYSGKGLDPKLANMFESQTGIKINIIKDKEQMAKMNAPDSKADLFMGMDVSTFAKLQNDSKLAPAKSKIIDSIVPANLKDENNEWIGLSKRARVIVYNKKAIDPKLIQNYEDLAKPELKGKLLMRTSNVSFNRSLLAFIIANDGEDKAKEWAKGTLNNLARDPKGGDREQARGVYEGIGAVGVMNSYYIITLLNSKKQSDQETAKSLGVIFPNQDGRGTHINITGIALLKSSQNKDAAIKFIEFMLSKEAQEILVSTSHEYPVNKDAKPSKEIAALGKFKEDSISLNKVANELENAQKIYKELGWK
>NZ_CP018788.1|WP_086301985.1|171189_173046_+|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552
MKKALLAILAIIVLIGFVLFNKDISSKKAQPDMAGAVSKDVVTMSDDDPRFNVWGKNFPEHMDMYQTVETEAPFETEFGGNHSYSKLIRYPQLTILWAGYPFSIDANEERGHFWIQVDQMDTARNNKDFLNSHGFAAFNGQPAACMNCHSGWTKWLENNAALGDTPREKWVSFNSAKYWTMVKNIPALEGITENSPEHSGPHGGKRMGVACADCHVPNTMELRVTRTALINALTKWRGYEPDPVTGVKATRSEMRSLVCAQCHVEYYFRPTGEKVKTIGESIASDTDKKWWNGTQKTYDEFDSWRDGNKATEIEVAGIELVFPWKQWGKNKPFRIEMFDEYYDENVTRSIFPQDWAHKITKAPMLKIQHPETELYSSSVHAANGVSCADCHMPYVRKGSSKVTNHNVTSPLKDINAACKSCHTQSEEYLKAQIQDIQRSIAFDLRSVEYATVSLINDIKNMRDRLAALPEFQTDGKADDKKISAVLKEVLELHRKGQMRGDFVGAENSTGFHSPREASRMLLQALEMARMGQTKLAEIALQYGFSDFKTSNLGFEDIQKLNPGEIRYKVDLNDARQSTAKGHKAGDRYYEHDNINDGPNAKLLELDKNNKPYNHKVLD
>NZ_CP018788.1|WP_086303185.1|170660_171131_+|cytochrome-c-nitrite-reductase-small-subunit
MWFLVVVVIIIVAAGYTFYNAKGMSYFSDDSAACNNCHVMNDVYASWRKSAHSREINGKPIASCNDCHLPNEFVDKWIAKAQSGVSHAYAFTFKLDDLPQNFTATKMSKNMVQANCVRCHSQMVSVVVNPTTKINHANEQLSCVKCHASVGHTRGF
>NZ_CP018788.1|WP_086235117.1|169138_170455_+|MATE-family-efflux-transporter
MSSKQLSLKALSVPIFFELFLRYLSLIINTLMVAAHSNFLVGAMGAGNQILDIFITIFTFLSIGCSVVITQAIGARDKILARKAIHQSLFLNSILGLICAAGIVWHGELILELMNVPKELMAQSSIYLYMLGICLFFDAVGIVLASIIRVYNRAYSVMFVTILMDGVTLIGNYYVLNFTQSELFGVGLSTIIGRVVAIIILIFILIYILKFIPKFSEFIKLERAVISKIIKIGGWAAGENLLWIVQYTIAFGFVASLGKENLSVQTIYFQISLFIMLIGQAISVANEIIIGKLVGAKKLQIAYKHTWRALYVSVLASFLVAFASFLAQDETMNALNLNPSLKELMIPLFTLSIFLEVVRTFNIIMVNSLRASGDAKFCFFSGVVFMFGVSLPVGYILCFNFGLGILGVWIGFCADEALRGFVNSWRWKSKKWQTKAVV
>NZ_CP018788.1|WP_086301984.1|167040_168822_-|phosphoethanolamine-transferase
MPVKLKNILELSFVFIYAIIGVVEIFLVMNFSNILNPIFFDTFLSTEPNEAIEFMQSYFSFNVALAVFGFIGVSILFFYFPIKFSPKPLNPKIYFALFLIISIVIFSKGTRYLEPNKFILGGWFVTIKDTITEQNSYLNEFKKLAKILDTQMKQDYNLTIKSQIPKVVLIISESTQRNYQSLYGFKLDTTPNLNALKASGNLFEFSDTIAPESHTNPALAKLLTFSNYENSQSSKWYEHMNIIDLMKIAGYKTQWFSNQEAVSVFGNIPEVISSRADIREFTRVGTSLELKNDFDEKLLEVYSKYRVKADREFHIFHLMGTHMAYANRFDKNNKNVRYFDMDELKNANLDIYPNGDKISNKGLKEKLNYINAIAYNDYVVSEIFKLYKDENAIIFYISDHADEVYDFREFKGHTSTMASRYMIEIPFMIYLSDKFKSSNPQLIQKIQKAQNKPFMSDDFIHGFMDILGIFSNDLDLSRSLFSDEFDANRIRIFSGKDYDKELKIDYPFASPSKIWLHRTNEPKKLADFKNIYQNFEIDVHFIDGYFDVGHDGKKYSIGLNLKDMLQITNNQNGGGHSPHIWLDFKNLTKENEK
>NZ_CP018788.1|WP_086303187.1|183486_184527_-|VWA-domain-containing-protein
MVNNALNLDNLGDLKYQKKVLGDFGDLSDIAASSKGFGNQKGNLNRYSIAQILNYFNMIKNNKALMDICDILGRMQNEEKELYKEKIMELTAYSYTQTTPTKRYKEEIIGITLGNDLENIVPQEMSLLDDEDLELLFDLKYIENRLFCFEKQGLISNQEEGQKEIEKEIEKERKKEDQKGPIIICVDTSGSMQGSPETIAKAITLMLTAKAKKENRNCYLINFSTSTICTDMSGAMGINKINDFLELSFNGGTDVGAGLRVGVEQMNKENYKNSDLLVISDGDFGYIDSNLHKQIEEKRKQKNKFYLLDVDGNSGKKDFFDKHWVYDSNTKNIRILCELKQQMKDD
>NZ_CP018788.1|WP_086301991.1|185091_187245_-|BspA-family-leucine-rich-repeat-surface-protein
MPNYEKRIKETIETLKSGLFEREECLKLVLLSMFAGKSIFLYGPPGTAKSMIARRASLAFKITDNSQDESKESNNGFFAYLMNRFSTPEEIFGPIDIAELKKNNLTRKTDGYLPTAHFAFLDEIWKSSPAILNTLLTIINERIYRDGNKDIKVPLKGVVCASNEFPPDNQGLEALYDRMILRYFVKPLEERENFKKLFKSKKSNDIKPLEPFSITELEQIAIKSQDIKFEQNTMDLICDLKSQIQLLNQDKEYRKKLLSSDEYKPIYISDRRWKQCAELLQTAALLSDRDAVERYDLALLAHLLWSSEEDKAIIEKILFNVLNENSNFDSELKALKEDNLNLKNLIEKNLYSPNGKPKKVDNNDKNKYLQISKDQITKANNLKNNIEAEFQKAKASIKNPFLSQNDIELSLSSYTLPLKEVNNEILKAKELENIIQNQPVNEKLKKASSAEYKYHPKTNEELRELVSHESVKLSEIDISEVSDLYELFKDSQRSDFSGIEEWDVSHVTNMRNMFIGIENFNSDISNWDVSNVTNMNYMFAGAVNFNSDISSWNVSKVTDMGYMFYNATSFNQPLDNWDVSNVTDMSGMFQGAFRFNQPLNNWDVSKVTNMSGMFATTYNNTSFGFFYNNKTPTIFNQPLNNWDVSSVTDMSGMFLGNESFNQFLNDWNVSNVINISRMFYNAKSFNQPLASWKISINVNKTLAFEGSAQNPLPRWYE
>NZ_CP018788.1|WP_086229311.1|187247_189446_-|dynamin-family-protein
MENLLKMSQTLENLVQENDLVGELQGIEKEHGIRPSAELKEALDEKMEPERDLKIGILGRVKAGKSSLLNALVFKGQNVLPKAATPMTAALTVLEYGDRFEASIEYYSQDEIETIKSNHATCQKILEDHQNAKFTELKQNNRKGESDSKLQESARKDAIKKLKDEVSLYAYYEQYEQIKKSGINASSIGEKEILTCSSYDELNEKLKNYVGSSGEYTPFTKSITLKLNEEMLKDVKIIDTPGVNDPIVSREDRTKELIAKCDVVFLVSPAGQFLNDVDLELLSNVNEKNGIKEFHIVASQFDLQLSAPEIIGNGVLDEAIQRALTPLSRQQKTVFENKKSSYNDKIYEQLTRFNVLYSSGISTEIINNYDNLQDENATHALGLFKKHYPDYFSNKETAISNLKKLSNIDEILKVLENVRKEKDEIIKGIMDDFISSKKSALNQYKNEIGAIINKKIEVLNSTDIEELKAQIEKIKSVKSKVVINANAAFEDSGAELSSKLKEKLNTQIKALFGGISSASENAKGSETVTKTKRVEDGRVLGFLWKKYKDVNYQVSIDTLNASSLRTAAQDAVIEISNILGDVYSDNIRMWKKTILKDLLTSLQESVGDEALDADMIKQSVRNIIANISLPEFSYDTTLPAALQKSGKLVGYERDEFLNALESFQSELRSRTNADIKAICATLDKAISNANIGDKFINSYEEKIEQLAKDAQDKESSLARYRSILDQLNQIEG
>NZ_CP018788.1|WP_086301992.1|189458_191168_-|dynamin-family-protein
MTNKQKSYIECGNKAINIAQNTDCLNDKIQELSLLTKSIENQELLVPVIGGFSSGKSSLINSFLGSEVLGIGITPQTAIATELRYSQDEKIEAIKDDDSIEIFDIKDLKKVEEKAQTYNHIKLYLNNQKLKEIDPIVLVDMPGFNAPIDTHNKAISRYMPSGVYFIALLSGVDEKTITKTYITELNGIHTRGKEFQLCISKTNLLPQRDIEQIKSYAKDTLEMEFGYSKDIELLDDNSGAKLEKILKDIDIESLFESIYKPHISMNLKEMESTINTTISALRYDKQDAINAIDELKNGISQIEIEKKKAIDNANSKYNDTNIEGIIGVVSSALSNNATTLAQSALNGGDIQSAINNIINSVLPSEIQKRLSGIQQNVIDNFKLSIGNIDMKASDIQTWADGLKEIVSGACFVANTLLNSDINKKSSSALVSSAIGIGGGALATQALAKIGFTINPIVGTILSAVFAILPGIFGKIADSKRLEAVKEQVRNEVIPSILSQIRPKLNEYFAKTTNEIINAISQEFTQKMSEKEDEIKNAQKEKELAISEVEDKISYLEDRRVEIQALIKNI
>NZ_CP018788.1|WP_086301993.1|191412_191877_-|hypothetical-protein
MKAKYAIAAIALGAAGFMAKKWLDKEVEKSRKIYGDDYSIKDTLLDKFENGLWKSYDALERVEETTLTALDKLQTKITGKEVDHRTILDLNEVSPEMREALLKIFGAMSMNAGFNEGANKSEPCGADQAQPLNTNACETNQSEPCDTNTGEKER
>NZ_CP018788.1|WP_180381652.1|192261_192426_-|hypothetical-protein
MCLRLGDAIKLLNKFDELGKDFNLLNGAKKHTYKELFIKYMDKKIVDISVWYIS
>NZ_CP018788.1|WP_180383468.1|192461_192635_-|hypothetical-protein
MANISKACLSDKDIELLEIINKRYFAVVGNTKELEIYINPKGSKVFQLLFMTNMAKT
>NZ_CP018788.1|WP_115633444.1|193320_193578_+|hypothetical-protein
MLFWILVARLGDKVAFSLASILDLGLMADINLAVNQADGRDAHTPYTQAQSLDGRLVQKNISSAMITIVSHNVKYDENDCKKSKN
>NZ_CP018788.1|WP_086301994.1|194327_194942_+|hypothetical-protein
MKSLTFDEIYQDLKSLEYDYLQPTLDRILAEEPRYIENFNKVFANLTDNAYLELKQLFMEFGLDFIDFNKEIQAKKKAIWKIRCSLKDGYTLVPLIASATFTALNDYIENLKKQKELGIPIVDIGNIHGKETIETLNKISSILNQTNSNYKYINLQALKNDYNVKLAQIAKKYRISLGKFRAFVAFEQIFKTTKSSKKRKIKII
>NZ_CP018788.1|WP_086301995.1|195042_195273_+|hypothetical-protein
MAGIDILNSTDYLTISDVETIYHIKRANHAKLRMAKNQNPNNPFLFSKIGKIILYKRSDIENFINGNIRRYDENGI

Crispr_ID: NZ_CP018788_3

• CRISPR_ID: NZ_CP018788_3
• CRISPR_location: 185590-185692
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers
• Cas_protein_info: WYL

Consensus repeat of NZ_CP018788_3

Consensus_repeat	Method
CCAGCTAGATATATCTGAGTTAAAATTT	CRISPRCasFinder

spacers of NZ_CP018788_3

>3.1|185618|47|NZ_CP018788|CRISPRCasFinder
ACAGCACCAGCGAACATATAGTTCATATTGGTTACATTAGATACATC

CRISPR arrays and Neighbor proteins around NZ_CP018788_3

CRISPR arrays

The CRISPR arrays of NZ_CP018788_3

>merge|NZ_CP018788|3|185590-185692|CRISPRCasFinder
CCAGCTAGATATATCTGAGTTAAAATTTACAGCACCAGCGAACATATAGTTCATATTGGTTACATTAGATACATCCCAGTTAGATATATCTGAGTTAAAATTT

>NZ_CP018788|3|3|185590-185692|CRISPRCasFinder
CCAGCTAGATATATCTGAGTTAAAATTT	ACAGCACCAGCGAACATATAGTTCATATTGGTTACATTAGATACATC
CCAGTTAGATATATCTGAGTTAAAATTT

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018788.1|WP_086301988.1|178852_179980_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301995.1|195042_195273_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_181892509.1|195256_196270_+|AAA-family-ATPase	unknown	unknown	gnl|CDD|316042
NZ_CP018788.1|WP_086229311.1|187247_189446_-|dynamin-family-protein	unknown	unknown	gnl|CDD|206739
NZ_CP018788.1|WP_086301985.1|171189_173046_+|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552	unknown	unknown	gnl|CDD|225840
NZ_CP018788.1|WP_086303185.1|170660_171131_+|cytochrome-c-nitrite-reductase-small-subunit	unknown	unknown	gnl|CDD|274453
NZ_CP018788.1|WP_086301993.1|191412_191877_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301992.1|189458_191168_-|dynamin-family-protein	unknown	unknown	gnl|CDD|366045
NZ_CP018788.1|WP_086301997.1|197020_197446_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_180383468.1|192461_192635_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_115633444.1|193320_193578_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301989.1|180019_181432_-|dynamin-family-protein	unknown	unknown	gnl|CDD|366045
NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl|CDD|225253
NZ_CP018788.1|WP_086301986.1|173256_174237_+|extracellular-solute-binding-protein	unknown	unknown	gnl|CDD|270260
NZ_CP018788.1|WP_086301994.1|194327_194942_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_180381652.1|192261_192426_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_181892508.1|174552_177342_+|flagellar-hook-protein-FlgE	unknown	unknown	gnl|CDD|236263
NZ_CP018788.1|WP_086303187.1|183486_184527_-|VWA-domain-containing-protein	unknown	unknown	gnl|CDD|236815
NZ_CP018788.1|WP_086224945.1|178659_178839_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086301990.1|181447_183487_-|BspA-family-leucine-rich-repeat-surface-protein	unknown	unknown	gnl|CDD|184118

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	5.7e-32	106.1	0.0

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP018788.1|WP_086301989.1|180019_181432_-|dynamin-family-protein	gnl|CDD|366045	pfam00350, Dynamin_N, Dynamin family.	3.52866e-11
NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein	gnl|CDD|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	3.79289e-28
NZ_CP018788.1|WP_086301986.1|173256_174237_+|extracellular-solute-binding-protein	gnl|CDD|270260	cd13542, PBP2_FutA1_ilke, Substrate binding domain of ferric iron-binding protein, a member of the type 2 periplasmic binding fold superfamily. FutA1 is the periplasmic component of an ABC-type iron transporter and serves as the primary receptor in Synerchosystis species. The periplasmic iron binding protein plays an essential role in the iron uptake pathway of Gram-negative pathogenic bacteria and is critical for survival of these pathogens within the host. After binding iron with high affinity, FutA1 interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The iron- and thiamine-binding proteins belong to the PBPI2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	4.45307e-116
NZ_CP018788.1|WP_181892509.1|195256_196270_+|AAA-family-ATPase	gnl|CDD|316042	pfam13481, AAA_25, AAA domain. This AAA domain is found in a wide variety of presumed DNA repair proteins.	2.70164e-14
NZ_CP018788.1|WP_086229311.1|187247_189446_-|dynamin-family-protein	gnl|CDD|206739	cd09912, DLP_2, Dynamin-like protein including dynamins, mitofusins, and guanylate-binding proteins. The dynamin family of large mechanochemical GTPases includes the classical dynamins and dynamin-like proteins (DLPs) that are found throughout the Eukarya. This family also includes bacterial DLPs. These proteins catalyze membrane fission during clathrin-mediated endocytosis. Dynamin consists of five domains; an N-terminal G domain that binds and hydrolyzes GTP, a middle domain (MD) involved in self-assembly and oligomerization, a pleckstrin homology (PH) domain responsible for interactions with the plasma membrane, GED, which is also involved in self-assembly, and a proline arginine rich domain (PRD) that interacts with SH3 domains on accessory proteins. To date, three vertebrate dynamin genes have been identified; dynamin 1, which is brain specific, mediates uptake of synaptic vesicles in presynaptic terminals; dynamin-2 is expressed ubiquitously and similarly participates in membrane fission; mutations in the MD, PH and GED domains of dynamin 2 have been linked to human diseases such as Charcot-Marie-Tooth peripheral neuropathy and rare forms of centronuclear myopathy. Dynamin 3 participates in megakaryocyte progenitor amplification, and is also involved in cytoplasmic enlargement and the formation of the demarcation membrane system. This family also includes mitofusins (MFN1 and MFN2 in mammals) that are involved in mitochondrial fusion. Dynamin oligomerizes into helical structures around the neck of budding vesicles in a GTP hydrolysis-dependent manner.	3.19345e-11
NZ_CP018788.1|WP_086301985.1|171189_173046_+|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552	gnl|CDD|225840	COG3303, NrfA, Formate-dependent nitrite reductase, periplasmic cytochrome c552 subunit [Inorganic ion transport and metabolism].	2.16953e-155
NZ_CP018788.1|WP_181892508.1|174552_177342_+|flagellar-hook-protein-FlgE	gnl|CDD|236263	PRK08425, flgE, flagellar hook protein FlgE; Validated.	7.90715e-166
NZ_CP018788.1|WP_086303187.1|183486_184527_-|VWA-domain-containing-protein	gnl|CDD|236815	PRK10997, yieM, ATPase RavA stimulator ViaA.	7.68634e-47
NZ_CP018788.1|WP_086303185.1|170660_171131_+|cytochrome-c-nitrite-reductase-small-subunit	gnl|CDD|274453	TIGR03153, cytochr_NrfH, cytochrome c nitrite reductase, small subunit. Members of this protein family are NrfH, a tetraheme cytochrome c. NrfH is the cytochrome c nitrite reductase small subunit, and forms a heterodimer with NrfA, the catalytic subunit. While NrfA can act as a monomer, NrfH can bind to and anchor NrfA in the membrane and enables electron transfer to NrfA from quinones. [Energy metabolism, Electron transport].	1.33363e-53
NZ_CP018788.1|WP_086301992.1|189458_191168_-|dynamin-family-protein	gnl|CDD|366045	pfam00350, Dynamin_N, Dynamin family.	3.53266e-15
NZ_CP018788.1|WP_086301990.1|181447_183487_-|BspA-family-leucine-rich-repeat-surface-protein	gnl|CDD|184118	PRK13531, PRK13531, regulatory ATPase RavA; Provisional.	3.00623e-79

Protein sequences

>NZ_CP018788.1|WP_086303187.1|183486_184527_-|VWA-domain-containing-protein
MVNNALNLDNLGDLKYQKKVLGDFGDLSDIAASSKGFGNQKGNLNRYSIAQILNYFNMIKNNKALMDICDILGRMQNEEKELYKEKIMELTAYSYTQTTPTKRYKEEIIGITLGNDLENIVPQEMSLLDDEDLELLFDLKYIENRLFCFEKQGLISNQEEGQKEIEKEIEKERKKEDQKGPIIICVDTSGSMQGSPETIAKAITLMLTAKAKKENRNCYLINFSTSTICTDMSGAMGINKINDFLELSFNGGTDVGAGLRVGVEQMNKENYKNSDLLVISDGDFGYIDSNLHKQIEEKRKQKNKFYLLDVDGNSGKKDFFDKHWVYDSNTKNIRILCELKQQMKDD
>NZ_CP018788.1|WP_086301990.1|181447_183487_-|BspA-family-leucine-rich-repeat-surface-protein
MYKTKIENIIKELSSGLFEREECLKLVLLSMFAGKSIFLYGPPGTAKSMIARRASLAFKITDNSQDESKESNNGFFAYLMNRFSTPEEIFGPIDIAELKKNNLTRKTDGYLPTAHFAFLDEIWKSSPAILNTLLTIINERIYRDGNKDIKVPLKGVVCASNEFPPDNQGLEALYDRMILRYFVKPLEERENFKKLFKSKKSNDIKPLEPFSITELEQIAIKSQDIKFEQNTMDLICDLKSQIQLLNQDKEYRKKLLSSDEYKPIYISDRRWKQCAELLQTAALLSDRDAVERYDLALLAHLLWSSEEDKAIIEKILFNVLNENSNFDSELKALKEDNLNLKNLIEKNLYSPNGKPKKVDNNDKNKYLQISKDQITKANNLKNNIEAEFQKAKASIKNPFLSQNDIELSLSSYTLPLKEVNNEILKAKELENIIQNQPVNEKLKKASSAEYKYHPKTNEELRELVSHESVKLSEIDISEVSDLYELFKDSQRSDFSGIEEWDVSHVTNMRNMFIGIENFNSDISNWDVSNVTNMNYMFAGAVNFNSDISSWNVSKVTDMGYMFYNATSFNQPLDNWDVSNVTDMSYMFAGATSFNQPLDNWDVSNVTDMSYMFAGATSFNQPLDNWDVSNVKNMENMFFSGADVVDTFAAGLLSAVGAARGAVAKQQLPNKKRLPKWYKE
>NZ_CP018788.1|WP_086301989.1|180019_181432_-|dynamin-family-protein
MQELQIINEILSAKPNNQTLSSFNKYLNNFYDITKKIAVENERDLVLNLKAIESEMAIIAAYAELFSKHVIAVGGGFSAGKSAFVNSFLKSKDIQLPISIDPTTAIPSYVMSSDKDQIIGISKNNGVANLGKIAPDILSRLTHNADNRLNFSFNLKDILPFLVVSSEFNDPKYQNICFIDTPGYNPNSDGNRAQDFNTAKEFLANSSSLLWLISCDASGGNITESDIKFLNSIGLENKKLYFIITKADKRPKSDLDEVLENLKDTLDMEGIEYEGISLYSSTDIEEYGYHKLSLFDFILSQINNKHSKSQENVMTNLIRVYQSYEKALVKKQDDNDRIFSVLHSITIEMAYIDDEENEEHTFKVDQYAKNLKSIFSSTYSDECKKLLKELTKAFKELKSSIDAIFGAVYDWDADANKITTKDIEQLSDLRKTIDLDGDDDLPKKPKGSTKAIQEANSAVQKTGFFNFEVK
>NZ_CP018788.1|WP_086301988.1|178852_179980_-|hypothetical-protein
MHNLLILYNPRYNSDLIKEHLELLKECGKVAFGKVRVKNNNMPHPFKGELEKIYSDTNPDSFTQLFITDYSNLYVAKVVKISSDDHTPIAPKYYQEQNLLVESWFVITDMREIYRNEFESVRDYFLSRITLPLRDNHTYALYGNNYVYPLIIDQDQNYFEDETLHHTDIYKTKKYLKTKKTLSRYCFGTNIDKLMSDTIDAVVLAEIEYIQNQKNMSNDFSSILVKYSKSVEREFYSLFKALFAYLCYNNSGLLTIRYDVQGIKYQLKDIFTHKPNLGSYGYLMKQSEISSTFENLVPNDIKNGFYYKILNFMHILKDIRNENIHGKNATIKETQKIRNAILGIGQESILITCLELKSKLNALYKESKIDRSKQI
>NZ_CP018788.1|WP_086224945.1|178659_178839_-|hypothetical-protein
MNGFVPHIQTLKCPKCGKKKVITAGCVINFYSCPKCNTIMIPSSGNFIDKLIGKLKGGR
>NZ_CP018788.1|WP_086301987.1|177742_178663_-|WYL-domain-containing-protein
MNSNGSNGENMIRRLMIMLKMLYLGQGLNPSELCSEFNLSLRTLQRDIARLKEYCAVDIQKGKDGKYYISRTEYEDGLLSFGDIKTFAKRSGVADLYPKLDTPMIADILSTTISKSLIVSSEPKQDSKELKDLFELLSDAILEHCVISFYYNDSQRTIKPYKLINTAGVWYLLGDEKAKLKHFTLSKIKSYKPLDQHFTPSNTFLKRIESNNLKWFSTSLKNAKILVLPKAREYFERKQVFKSYKLIKDDENGILLDVEFAFDDELLNIIKAWIPYIKIIEPQELDTKLKDILKSYINDEPISNLA
>NZ_CP018788.1|WP_181892508.1|174552_177342_+|flagellar-hook-protein-FlgE
MMGALWSGVTGLQAHQVAMDVEGNNIANVNTVGFKYSRASFADLFSQTQKVATAPQGDLGGKNSMQIGLGSTVNTVTKIFKQGTIQTTDKQSDMAIQGDGFFVVSADGGKTYMYTRNGDFSLDSKGNFVDRNGYVVQGWMRNEDTGTIDPTSPLSNIIIEPGMAMEANPTSELAIIANLNSGSNIGAKNSPIYTLDHYNDFLDANGNGLWEDGETKNPNDLSNNTYYINSNKEVAVKEAGVDLGVVFNGSGEGLNLREGQGIWVSYADAKATFGELPNNAGQGTNKYKLHISINGIEIPATELTKMDEVVKKINDYTPQTGVIATLNGDKGIQLTNTNNQGTTDATKNIKIKKLEDDTTSIRTTSVITAYKYTYSSGAGKTADHNYNDGAARVVKTTEDLRRAMQTDAREYVNYSGSNVSNAVNGATYITNKILGIIDAAGNVQTAKQNVRNQIQRALQDGQATFNGFKNNGAITEPISEAAVGVMVSILNSSDQIMQNQQITTINDLKEAIRELVTNDKLAEFASREWDSPLDADGDGNFNNNTANDLPAPEADGSHANGTYRDINLNDGVQVTVNEKGQFVFRNPAGDASYGQNDGHTIVNQNQQGGTKVEDSADAYTDTNGQKKTPANADTYTNDYAMQIAVSGYSNAAQNVNENSALADVFKALGGSLATGTGEKVSSNLTMSSHAATTEIYDSLGSKHEIKFEWRKVSYSPENGTEWSVLIQVPEPGVLNTDGSGFSNVVSGSARFNNDGTLLGFTPTTLSFTANNGSAPGQGIELNFGKIGDSNGLRSNDNPSATDNIIQDGYTAGNLVGTRIDEAGTIIGSFSNGRSFGLAQVSLAVFSNNEGLESRSGNIFSQTANSGDPIFGAAGTSRRGTITASALEMSNVDLSRALTQLIVVQRGYQANSKTITTSDQMLTSLLQIKQ
>NZ_CP018788.1|WP_086301986.1|173256_174237_+|extracellular-solute-binding-protein
MKKLLLTAAFACMALANEINLYSGKGLDPKLANMFESQTGIKINIIKDKEQMAKMNAPDSKADLFMGMDVSTFAKLQNDSKLAPAKSKIIDSIVPANLKDENNEWIGLSKRARVIVYNKKAIDPKLIQNYEDLAKPELKGKLLMRTSNVSFNRSLLAFIIANDGEDKAKEWAKGTLNNLARDPKGGDREQARGVYEGIGAVGVMNSYYIITLLNSKKQSDQETAKSLGVIFPNQDGRGTHINITGIALLKSSQNKDAAIKFIEFMLSKEAQEILVSTSHEYPVNKDAKPSKEIAALGKFKEDSISLNKVANELENAQKIYKELGWK
>NZ_CP018788.1|WP_086301985.1|171189_173046_+|ammonia-forming-cytochrome-c-nitrite-reductase-subunit-c552
MKKALLAILAIIVLIGFVLFNKDISSKKAQPDMAGAVSKDVVTMSDDDPRFNVWGKNFPEHMDMYQTVETEAPFETEFGGNHSYSKLIRYPQLTILWAGYPFSIDANEERGHFWIQVDQMDTARNNKDFLNSHGFAAFNGQPAACMNCHSGWTKWLENNAALGDTPREKWVSFNSAKYWTMVKNIPALEGITENSPEHSGPHGGKRMGVACADCHVPNTMELRVTRTALINALTKWRGYEPDPVTGVKATRSEMRSLVCAQCHVEYYFRPTGEKVKTIGESIASDTDKKWWNGTQKTYDEFDSWRDGNKATEIEVAGIELVFPWKQWGKNKPFRIEMFDEYYDENVTRSIFPQDWAHKITKAPMLKIQHPETELYSSSVHAANGVSCADCHMPYVRKGSSKVTNHNVTSPLKDINAACKSCHTQSEEYLKAQIQDIQRSIAFDLRSVEYATVSLINDIKNMRDRLAALPEFQTDGKADDKKISAVLKEVLELHRKGQMRGDFVGAENSTGFHSPREASRMLLQALEMARMGQTKLAEIALQYGFSDFKTSNLGFEDIQKLNPGEIRYKVDLNDARQSTAKGHKAGDRYYEHDNINDGPNAKLLELDKNNKPYNHKVLD
>NZ_CP018788.1|WP_086303185.1|170660_171131_+|cytochrome-c-nitrite-reductase-small-subunit
MWFLVVVVIIIVAAGYTFYNAKGMSYFSDDSAACNNCHVMNDVYASWRKSAHSREINGKPIASCNDCHLPNEFVDKWIAKAQSGVSHAYAFTFKLDDLPQNFTATKMSKNMVQANCVRCHSQMVSVVVNPTTKINHANEQLSCVKCHASVGHTRGF
>NZ_CP018788.1|WP_086229311.1|187247_189446_-|dynamin-family-protein
MENLLKMSQTLENLVQENDLVGELQGIEKEHGIRPSAELKEALDEKMEPERDLKIGILGRVKAGKSSLLNALVFKGQNVLPKAATPMTAALTVLEYGDRFEASIEYYSQDEIETIKSNHATCQKILEDHQNAKFTELKQNNRKGESDSKLQESARKDAIKKLKDEVSLYAYYEQYEQIKKSGINASSIGEKEILTCSSYDELNEKLKNYVGSSGEYTPFTKSITLKLNEEMLKDVKIIDTPGVNDPIVSREDRTKELIAKCDVVFLVSPAGQFLNDVDLELLSNVNEKNGIKEFHIVASQFDLQLSAPEIIGNGVLDEAIQRALTPLSRQQKTVFENKKSSYNDKIYEQLTRFNVLYSSGISTEIINNYDNLQDENATHALGLFKKHYPDYFSNKETAISNLKKLSNIDEILKVLENVRKEKDEIIKGIMDDFISSKKSALNQYKNEIGAIINKKIEVLNSTDIEELKAQIEKIKSVKSKVVINANAAFEDSGAELSSKLKEKLNTQIKALFGGISSASENAKGSETVTKTKRVEDGRVLGFLWKKYKDVNYQVSIDTLNASSLRTAAQDAVIEISNILGDVYSDNIRMWKKTILKDLLTSLQESVGDEALDADMIKQSVRNIIANISLPEFSYDTTLPAALQKSGKLVGYERDEFLNALESFQSELRSRTNADIKAICATLDKAISNANIGDKFINSYEEKIEQLAKDAQDKESSLARYRSILDQLNQIEG
>NZ_CP018788.1|WP_086301992.1|189458_191168_-|dynamin-family-protein
MTNKQKSYIECGNKAINIAQNTDCLNDKIQELSLLTKSIENQELLVPVIGGFSSGKSSLINSFLGSEVLGIGITPQTAIATELRYSQDEKIEAIKDDDSIEIFDIKDLKKVEEKAQTYNHIKLYLNNQKLKEIDPIVLVDMPGFNAPIDTHNKAISRYMPSGVYFIALLSGVDEKTITKTYITELNGIHTRGKEFQLCISKTNLLPQRDIEQIKSYAKDTLEMEFGYSKDIELLDDNSGAKLEKILKDIDIESLFESIYKPHISMNLKEMESTINTTISALRYDKQDAINAIDELKNGISQIEIEKKKAIDNANSKYNDTNIEGIIGVVSSALSNNATTLAQSALNGGDIQSAINNIINSVLPSEIQKRLSGIQQNVIDNFKLSIGNIDMKASDIQTWADGLKEIVSGACFVANTLLNSDINKKSSSALVSSAIGIGGGALATQALAKIGFTINPIVGTILSAVFAILPGIFGKIADSKRLEAVKEQVRNEVIPSILSQIRPKLNEYFAKTTNEIINAISQEFTQKMSEKEDEIKNAQKEKELAISEVEDKISYLEDRRVEIQALIKNI
>NZ_CP018788.1|WP_086301993.1|191412_191877_-|hypothetical-protein
MKAKYAIAAIALGAAGFMAKKWLDKEVEKSRKIYGDDYSIKDTLLDKFENGLWKSYDALERVEETTLTALDKLQTKITGKEVDHRTILDLNEVSPEMREALLKIFGAMSMNAGFNEGANKSEPCGADQAQPLNTNACETNQSEPCDTNTGEKER
>NZ_CP018788.1|WP_180381652.1|192261_192426_-|hypothetical-protein
MCLRLGDAIKLLNKFDELGKDFNLLNGAKKHTYKELFIKYMDKKIVDISVWYIS
>NZ_CP018788.1|WP_180383468.1|192461_192635_-|hypothetical-protein
MANISKACLSDKDIELLEIINKRYFAVVGNTKELEIYINPKGSKVFQLLFMTNMAKT
>NZ_CP018788.1|WP_115633444.1|193320_193578_+|hypothetical-protein
MLFWILVARLGDKVAFSLASILDLGLMADINLAVNQADGRDAHTPYTQAQSLDGRLVQKNISSAMITIVSHNVKYDENDCKKSKN
>NZ_CP018788.1|WP_086301994.1|194327_194942_+|hypothetical-protein
MKSLTFDEIYQDLKSLEYDYLQPTLDRILAEEPRYIENFNKVFANLTDNAYLELKQLFMEFGLDFIDFNKEIQAKKKAIWKIRCSLKDGYTLVPLIASATFTALNDYIENLKKQKELGIPIVDIGNIHGKETIETLNKISSILNQTNSNYKYINLQALKNDYNVKLAQIAKKYRISLGKFRAFVAFEQIFKTTKSSKKRKIKII
>NZ_CP018788.1|WP_086301995.1|195042_195273_+|hypothetical-protein
MAGIDILNSTDYLTISDVETIYHIKRANHAKLRMAKNQNPNNPFLFSKIGKIILYKRSDIENFINGNIRRYDENGI
>NZ_CP018788.1|WP_181892509.1|195256_196270_+|AAA-family-ATPase
MKMEYNSTQSVEQNIHDIISKFGLEATSEMINNTKDEWIIPNFLAPQTITMIYASAGAGKSLFTLYLTKFLLQENKFSQIHYLDADNSPRVLKDRNLNQILDSFKDSFHYYFIDKPKNGDILTNLSKSNDLDGVLIIIDSIRNFINVDFTKDDKITSFLDKLQKLRNLGATIIFLHHQPKQIDDENNKAYKGSIAFMDSVDEGYYLSLIKEHSILGLNELFFTLEPQKFRFDMAISNFIINTDNFGFKKDDNLLFASNDIARYTAEYVIKILQKHANGLPKSKLIKELKDLAFRDDVEVYRKNSLWRFMDKFKNRLWTITREAKHNTIRYKLINSQF
>NZ_CP018788.1|WP_086301997.1|197020_197446_+|hypothetical-protein
MAESHVISALVAKHADLQGKIKSYQEAIKEERDEISTISKSIKIFDPNYDLRKIALKKTRERYFKHKELTKLVIEHIKSNDNVDINELTEYVMKAKALSQELHKSIYGGIYTVLENLVRQYIIECRVINDAKQYRIKILNA

Crispr_ID: NZ_CP018788_4

• CRISPR_ID: NZ_CP018788_4
• CRISPR_location: 1407086-1407180
• CRISPR_type: Orphan
• Repeat_type: NA
• Spacer_info: 1 spacers

Consensus repeat of NZ_CP018788_4

Consensus_repeat	Method
ACACCCTTTACAAAGTCAAAGCTC	CRISPRCasFinder

spacers of NZ_CP018788_4

>4.1|1407110|47|NZ_CP018788|CRISPRCasFinder
CCTAATTTTAACTTAGATAGCTTATTTAATGGGTATGAGTTCAATTC

CRISPR arrays and Neighbor proteins around NZ_CP018788_4

CRISPR arrays

The CRISPR arrays of NZ_CP018788_4

>merge|NZ_CP018788|4|1407086-1407180|CRISPRCasFinder
ACACCCTTTACAAAGTCAAAGCTCCCTAATTTTAACTTAGATAGCTTATTTAATGGGTATGAGTTCAATTCACACCCTTTACAAAGTCAAAGCTC

>NZ_CP018788|4|4|1407086-1407180|CRISPRCasFinder
ACACCCTTTACAAAGTCAAAGCTC	CCTAATTTTAACTTAGATAGCTTATTTAATGGGTATGAGTTCAATTC
ACACCCTTTACAAAGTCAAAGCTC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018788.1|WP_086302999.1|1416607_1417291_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086302954.1|1398212_1399361_+|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl|CDD|225114
NZ_CP018788.1|WP_086302961.1|1403969_1404470_+|site-specific-integrase	unknown	unknown	gnl|CDD|271182
NZ_CP018788.1|WP_086302956.1|1402037_1402946_+|radical-SAM-protein	unknown	unknown	gnl|CDD|223803
NZ_CP018788.1|WP_086302995.1|1414132_1415440_+|MFS-transporter	unknown	unknown	gnl|CDD|341025
NZ_CP018788.1|WP_086302991.1|1412294_1413140_-|phosphate-ABC-transporter-permease-subunit-PstC	unknown	unknown	gnl|CDD|223646
NZ_CP018788.1|WP_086302989.1|1411476_1412298_-|phosphate-ABC-transporter-permease-PstA	unknown	unknown	gnl|CDD|273373
NZ_CP018788.1|WP_086245210.1|1400463_1400991_+|YqhA-family-protein	unknown	unknown	gnl|CDD|377024
NZ_CP018788.1|WP_086302987.1|1410721_1411477_-|phosphate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl|CDD|224042
NZ_CP018788.1|WP_086302997.1|1415426_1416611_+|molybdopterin-molybdotransferase-MoeA	unknown	unknown	gnl|CDD|238452
NZ_CP018788.1|WP_086234988.1|1401006_1402038_+|uroporphyrinogen-decarboxylase	unknown	unknown	gnl|CDD|234644
NZ_CP018788.1|WP_086302969.1|1408303_1410013_-|PAS-domain-containing-protein	unknown	unknown	gnl|CDD|274368
NZ_CP018788.1|WP_086225568.1|1399436_1400471_+|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl|CDD|237845
NZ_CP018788.1|WP_086234974.1|1417691_1418048_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086302958.1|1403274_1403979_+|integrase-arm-type-DNA-binding-domain-containing-protein	unknown	unknown	gnl|CDD|170049
NZ_CP018788.1|WP_086302962.1|1404821_1405043_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086302966.1|1405595_1406357_+|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086302964.1|1405039_1405393_+|hypothetical-protein	unknown	unknown	gnl|CDD|271198
NZ_CP018788.1|WP_086302993.1|1413139_1413970_-|substrate-binding-domain-containing-protein	unknown	unknown	gnl|CDD|270371
NZ_CP018788.1|WP_086302984.1|1410014_1410686_-|response-regulator-transcription-factor	unknown	unknown	gnl|CDD|223816

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP018788.1|WP_086302954.1|1398212_1399361_+|sigma-54-dependent-Fis-family-transcriptional-regulator	gnl|CDD|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	2.57315e-164
NZ_CP018788.1|WP_086302956.1|1402037_1402946_+|radical-SAM-protein	gnl|CDD|223803	COG0731, COG0731, Fe-S oxidoreductases [Energy production and conversion].	4.12754e-55
NZ_CP018788.1|WP_086302961.1|1403969_1404470_+|site-specific-integrase	gnl|CDD|271182	cd00801, INT_P4_C, Bacteriophage P4 integrase, C-terminal catalytic domain. P4-like integrases are found in temperate bacteriophages, integrative plasmids, pathogenicity and symbiosis islands, and other mobile genetic elements. The P4 integrase mediates integrative and excisive site-specific recombination between two sites, called attachment sites, located on the phage genome and the bacterial chromosome. The phage attachment site is often found adjacent to the integrase gene, while the host attachment sites are typically situated near tRNA genes. This family belongs to the superfamily of DNA breaking-rejoining enzymes, which share the same fold in their catalytic domain and the overall reaction mechanism. The catalytic domain contains six conserved active site residues. Their overall reaction mechanism involves cleavage of a single strand of a DNA duplex by nucleophilic attack of a conserved tyrosine to give a 3' phosphotyrosyl protein-DNA adduct. In the second rejoining step, a terminal 5' hydroxyl attacks the covalent adduct to release the enzyme and generate duplex DNA.	6.02576e-50
NZ_CP018788.1|WP_086302995.1|1414132_1415440_+|MFS-transporter	gnl|CDD|341025	cd17472, MFS_YajR_like, Escherichia coli inner membrane transport protein YajR and similar multidrug-efflux transporters of the Major Facilitator Superfamily. This family is composed of Escherichia coli inner membrane transport protein YajR and some uncharacterized multidrug-efflux transporters. YajR is a putative proton-driven major facilitator superfamily (MFS) transporter found in many gram-negative bacteria. Unlike most MFS transporters, YajR contains a C-terminal, cytosolic YAM domain, which may play an essential role for the proper functioning of the transporter. YajR-like transporters belong to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	4.21866e-107
NZ_CP018788.1|WP_086302991.1|1412294_1413140_-|phosphate-ABC-transporter-permease-subunit-PstC	gnl|CDD|223646	COG0573, PstC, ABC-type phosphate transport system, permease component [Inorganic ion transport and metabolism].	3.27304e-77
NZ_CP018788.1|WP_086302989.1|1411476_1412298_-|phosphate-ABC-transporter-permease-PstA	gnl|CDD|273373	TIGR00974, 3a0107s02c, phosphate ABC transporter, permease protein PstA. This model describes PtsA, one of a pair of permease proteins in the ABC (high affinity) phosphate transporter. In a number of species, this permease is fused with the PtsC protein (TIGR02138). In the model bacterium Escherichia coli, this transport system is induced when the concentration of extrallular inorganic phosphate is low. A constitutive, lower affinity transporter operates otherwise. [Transport and binding proteins, Anions].	1.87133e-67
NZ_CP018788.1|WP_086245210.1|1400463_1400991_+|YqhA-family-protein	gnl|CDD|377024	pfam03350, UPF0114, Uncharacterized protein family, UPF0114.	2.76378e-31
NZ_CP018788.1|WP_086302984.1|1410014_1410686_-|response-regulator-transcription-factor	gnl|CDD|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	8.44378e-77
NZ_CP018788.1|WP_086302997.1|1415426_1416611_+|molybdopterin-molybdotransferase-MoeA	gnl|CDD|238452	cd00887, MoeA, MoeA family. Members of this family are involved in biosynthesis of the molybdenum cofactor (MoCF), an essential cofactor of a diverse group of redox enzymes. MoCF biosynthesis is an evolutionarily conserved pathway present in eubacteria, archaea and eukaryotes. MoCF contains a tricyclic pyranopterin, termed molybdopterin (MPT). MoeA, together with MoaB, is responsible for the metal incorporation into MPT, the third step in MoCF biosynthesis. The plant homolog Cnx1 is a MoeA-MogA fusion protein. The mammalian homolog gephyrin is a MogA-MoeA fusion protein, that plays a critical role in postsynaptic anchoring of inhibitory glycine receptors and major GABAa receptor subtypes.	7.54731e-128
NZ_CP018788.1|WP_086234988.1|1401006_1402038_+|uroporphyrinogen-decarboxylase	gnl|CDD|234644	PRK00115, hemE, uroporphyrinogen decarboxylase; Validated.	0
NZ_CP018788.1|WP_086302969.1|1408303_1410013_-|PAS-domain-containing-protein	gnl|CDD|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	1.45972e-61
NZ_CP018788.1|WP_086225568.1|1399436_1400471_+|aspartate-semialdehyde-dehydrogenase	gnl|CDD|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	0
NZ_CP018788.1|WP_086302958.1|1403274_1403979_+|integrase-arm-type-DNA-binding-domain-containing-protein	gnl|CDD|170049	PRK09692, PRK09692, integrase; Provisional.	1.12983e-17
NZ_CP018788.1|WP_086302964.1|1405039_1405393_+|hypothetical-protein	gnl|CDD|271198	cd04434, LanC_like, Cyclases involved in the biosynthesis of lantibiotics, and similar proteins. LanC is the cyclase enzyme of the lanthionine synthetase. Lanthionine is a lantibiotic, a unique class of peptide antibiotics. They are ribosomally synthesized as a precursor peptide and then post-translationally modified to contain thioether cross-links called lanthionines (Lans) or methyllanthionines (MeLans), in addition to 2,3-didehydroalanine (Dha) and (Z)-2,3-didehydrobutyrine (Dhb). These unusual amino acids are introduced by the dehydration of serine and threonine residues, followed by thioether formation via addition of cysteine thiols, catalysed by LanB and LanC or LanM. LanC, the cyclase component, is a zinc metalloprotein, whose bound metal has been proposed to activate the thiol substrate for nucleophilic addition. A related domain is also present in LanM and other pro- and eukaryotic proteins with poorly characterized functions.	0.00422314
NZ_CP018788.1|WP_086302993.1|1413139_1413970_-|substrate-binding-domain-containing-protein	gnl|CDD|270371	cd13653, PBP2_phosphate_like_1, Substrate binding domain of putative ABC-type phosphate transporter, a member of the type 2 periplasmic binding fold superfamily. This subfamily contains uncharacterized phosphate binding domains found in PstS proteins that serve as initial receptors in the ABC transport of phosphate in eubacteria and archaea. After binding the ligand, PstS interacts with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. The PstS proteins belong to the PBP2 superfamily of periplasmic binding proteins that differ in size and ligand specificity, but have similar tertiary structures consisting of two globular subdomains connected by a flexible hinge. They have been shown to bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	1.09862e-37
NZ_CP018788.1|WP_086302987.1|1410721_1411477_-|phosphate-ABC-transporter-ATP-binding-protein	gnl|CDD|224042	COG1117, PstB, ABC-type phosphate transport system, ATPase component [Inorganic ion transport and metabolism].	3.44495e-176

Protein sequences

>NZ_CP018788.1|WP_086302966.1|1405595_1406357_+|hypothetical-protein
MAFSLIEAIYQSIGETEAQKALSNINAFNQPSSLNCDSLRFIATKSFYSKFTKWLAKLNIQMHETQINDKKFNLFDLLTPQAPKIAFESKITNKITLTTYYSSISFKKARQAKRTLNNFIIIELHGLAQYNPQSKIPIKLTNPIIRILKYIFKYCDNLKERKTLNLVSFDIALDYHDNEPITKEYAINKATYLDQIHAKFFNYQGTLYIQESKAPTAKNINSNLQKIIIYSKTTKNALPYPLNRFELRFLIND
>NZ_CP018788.1|WP_086302964.1|1405039_1405393_+|hypothetical-protein
MNPAKKLIAPKLRGSDKSAQMLLKALIDGKKITNHEISKYATNSVKDILGDLKRDYGLNLLDEWVRDPKTDIRYKKYYINKSGIAYARLLLSYFTTKNRAILAKLKIRVKAKEPKNV
>NZ_CP018788.1|WP_086302962.1|1404821_1405043_+|hypothetical-protein
MSNLDKFQNNGGIVLLDTKQLKTLLHIKGDATLWRYLKDGIIPQPRLIVSRSKRLWALDEVLSYLSKNKGGEI
>NZ_CP018788.1|WP_086302961.1|1403969_1404470_+|site-specific-integrase
MQLGAYTALRSGTIRALKWDYIDFKQNIINIPAELMKMKKPFILPISSQAKAILKELETYRLGQYLFSINSKIMSENTLNKAIKILGFGDEATFHGFRGLFSTICHENTQEHGLTSEVIELCLAHTDNNKVRSTYNKSERLQEKAQLMEWYGYYLNNLKKEQLLTS
>NZ_CP018788.1|WP_086302958.1|1403274_1403979_+|integrase-arm-type-DNA-binding-domain-containing-protein
MSFTTDSQLKSLTLTDDKKEQYVKDGSTKNLFILLRETSKTFIFRYKIDGSKIKSITIGQYPSISLAEARQKANEFKALLAKGIDPRDYTNEHELTFQDIADKWLQDRAKQKLTNYKDIQGRLNNHILPKIGNIKIKDLKRDKLNKCILEVKLKGAGKDGYETKQRIFIILRDILKYITIQGIIQDYTSPLAGLNFSDICKDKHEVSNHRFIKDPTKLREFLTAIDSYKGNKYS
>NZ_CP018788.1|WP_086302956.1|1402037_1402946_+|radical-SAM-protein
MGYKFIFGPVSSRRFGSSLGIDLSPDQKSCNFDCLYCELKKAKTIRVIKNGPNSKVIINELKNALNEFKDIDVITLTANGEPSLYSDLSNLITQINTLKTTQKSLILSNGSAVLNPNAIEALLNLDIVKFSLDSANQKTFRKIDRSIDNIDINKLVELMSQFRSKFKGELIMEVLVVAGYNDSDDEFMALNRAFKKILPNRIDISTIDRPPAHNVRGVSSETLHYLATFIDAAPVSIASRTPLKSKFDYSKDDLEKLLKLRPQSLYDIENNFTTNAKINLETLINEGKVIECDLAGMKFYRI
>NZ_CP018788.1|WP_086234988.1|1401006_1402038_+|uroporphyrinogen-decarboxylase
MIFIDACLGKKTPYTPVWMMRQAGRYLPEYMRVRAEAGDFLSLCKDYEKASEVTLQPVDILGVDAAILFSDILVVPMEMGMELKFVKGEGPVFPKPIATMEDLDRLSSDKAVKNLSYVYDTIKLTRDKLAKDKALIGFCGAPWTIATYMIEGGSTKTYNICKKMVYDNPQFLHAILRKVTNALKLYLAEQIKSGVNAVQIFDSWAGALEKSAYMEFGFSYINEIVDYLKANFPDTPIIVFPKGISGFLDDISGNFDVFGVDWSTPLANAKKSLGAKYILQGNMEPTRLYNKDAIDEGVDEILSIMGGKRHIFNLGHGILPDIPVEHAKYFIKSVQEKSAKYAK
>NZ_CP018788.1|WP_086245210.1|1400463_1400991_+|YqhA-family-protein
MDNIKNKIEKLFEGLLWKSRMVTLLPVIFGLLGAFVMFIVASYDIVKVIVYAWHYLILGDHSVDLHSDGVALIIGAIDLYLMALVFFIFSFGIYELFISEIDTIKSSRQARVLEVHSLDQLKDKIGKVIVMVLVVNFFQRVLHAKFTTPLEMVYLALSILALCLGLYFLHKSSHH
>NZ_CP018788.1|WP_086225568.1|1399436_1400471_+|aspartate-semialdehyde-dehydrogenase
MRKYSIAVVGATGAVGEEIFRVLEEMDFPVGDVLPLASAKSVGKEIEFKGKNYPIVELTDTVFDEHEVDIAFFSAGGSISAHFVPFAAASGAIVIDNTSHFRMDPEVPLVVPECNPGDIAQWQNKGIIANPNCSTIQMVQVLKPLDDAFGIQRVDVSTYQATSGAGKKGMEELVMQMQKFFEFKLDECEPSAFKHQIALNVIPHIDVFLDNDYTKEEMKMVKETQKILHKDIQVSATCVRVPVLRSHSESITIKFKTPIDAQKATQILKNAPSVVVQDSPKDNLYPMPIHASDTNETYVGRIRKDNYDDSILHLWCVADQIRVGAATNAVRIAQKWIEMQEQNG
>NZ_CP018788.1|WP_086302954.1|1398212_1399361_+|sigma-54-dependent-Fis-family-transcriptional-regulator
MNVVIVEDDINMRKSLEIALGDYNEFSVKSYKSATEALKKLSNDTDVIVTDINMPGMDGLEFIKELGGKYDVIIMTGNATLNRAIESVRLGVKDFLTKPFDIDTLATAIKRTSVITQKTKTKTPDTTTGIKSSNFLAASANLDKTLNIAKKAAQTDVSVMIMGESGVGKELFSRYIHENSKRKDSALMAINMAAIPENLLESELYGYEKGAFTDATATKKGLFELANGGTLFLDEIGEMPLNLQPKLLRAIQEREIVRVGASKPIKIDVRIVSATNANLEQKVANGEFREDLFYRLNTVPLKIPPLRERKDEIVDIANATLKRVCVEYELGKKEFSQEAIDELLNYDYPGNIRELISIVERAAILSEGSSISKEDLFIYAKK
>NZ_CP018788.1|WP_086302969.1|1408303_1410013_-|PAS-domain-containing-protein
MQKRVFYFIIFSTLALALFINIFLIFSIESVLKNELFDRLKNYAYSIKSEVLSSIQNGSIQSLKDLDETYRISIIDQNGVVIYDNLVNNLNLDNHSNRAEFKDAIEDGESTNIRYSNTLLKRNLYYGLKISNEKGEFVLRISKEQDYLYAIFMSFIPYIIAEIIAVLIFSFLLAKYLTHIILRPIQGIDLKNLDSNLPYPELRVLIETLKKQNKIIKSQFKHLKQKRQELQSLTKGMKDGIIIINRSGEILSINPSAQKYFANLAKHTNISQIQNDLFLKLLLQNLRDFKDGKISCEIREQIVFMQETLVECEIVFSPIFSQKGKFKGLIIVICDITEFKRNQNLSKEFSANVTHELKTPLTSIMGNAEMIRNNLVKSDDIPHFIDTIYNESKRLLHLIEDILKLSFLDESSTKNIPFAKVELKNLLLKVYSNLKSVAKKYDIEFKFELEEAYIHGSKELLEHAIFNLCDNAIKYNHPGGYVKIKIKNLKDCVELSIKDSGIGIEPSSQERIFERFYFVDKSYSKKVGGTGLGLSIVKSVLNMHHAKVKLKSQKDIGSEFIITFAKDIK
>NZ_CP018788.1|WP_086302984.1|1410014_1410686_-|response-regulator-transcription-factor
MIYVLEDEGAILDLICYALKSQNIPVKGFSLAKDFYKALKDEIPQILVLDVMLPDGDGFEILKDLKNSAKYKDICVLMLTALDSEINKVKGLDLGADDYIAKPFGVMELLARIRVIFRRKAKEEPNSDISFNGLEFSYKNHIVKVNGKPLELTLKEFELLGFLLQNPNQVFSRDMLLEMIWGYSYDKESRTIDMHIKTLRKKLGNMSDMIRTIHGVGYKLVRE
>NZ_CP018788.1|WP_086302987.1|1410721_1411477_-|phosphate-ABC-transporter-ATP-binding-protein
MKKCFDINKLNLHYGAFHALKNINMEITKGEVTAFIGPSGCGKSTFIKTLNRMNDLVEGCKIEGEILFHDRDIYSKDYDINLLRKRVGMVFQKPNPFAMSIYDNITFGPKTHGIKDKDTLDSIVEKSLKDAALWDDLKDRLYSSALGLSGGQQQRLCIARTLAVDPEVILMDEPTSALDPISTAKIEELVLKLKKDYTIIIVTHNMQQAHRISDKTAFFLMGEVIEYDDTKKIFNKPKNQKTQDYVMGKFG
>NZ_CP018788.1|WP_086302989.1|1411476_1412298_-|phosphate-ABC-transporter-permease-PstA
MSRDYLSIFLSFLLKFSIFSVLFVFFGITLFIFIKGIIYISPSLFEWEYNSTNVSLMPALINTINMVICSLAIAMPLGIFGAIYLNEYSKKDSKILNLIRVTSDTLVGIPSIVYGLFGYLAFVIYFGFKTSFIAGVLTLSIMILPLILRSSEEALKSVPMGYKEASLALGASKLRTIFAIILPSATAGILAGVILSIGRIVGESAALLYTSGSVAQIAGALDSGRTLSVHMYAISSEGLHINEAYSTAMVLIVIVFFMNFISNFVAKKILKDS
>NZ_CP018788.1|WP_086302991.1|1412294_1413140_-|phosphate-ABC-transporter-permease-subunit-PstC
MLKERFFQGLFALSAGFSIFAVGAIALFLFFNAFATISQIGFLEFIFGMDWYPDEEIFGIFPMIVGSIYVTALAIALGVPIGVLSAVYLAYFCPKGLKKIIMPAVELLGAIPSVVYGFFGLVIVVPLVSNIFDGVSGKSILAASLILAIMVLPTIILVSKVAIEALPKSYYEGALALGASPERTVFFAIVPAAKSGILASVILGVGRAIGEAMAVIMVAGNQVQIPHSLSDGVRTLTTNIVLEMGYAADLHKDVLIANAVVLFVFILIINISFSALKRGKK
>NZ_CP018788.1|WP_086302993.1|1413139_1413970_-|substrate-binding-domain-containing-protein
MFKKYLVALFVLFGLNSYLLAENIYPISREMGSGTRGAFVDIFDVKEQVGKKKIDATSKKAEVTNSTGVMITTVANSKNAIGYISLGSLNDSVKAVKIDGVAPSVENINNKTYTVFRPFNLAISSDNELVNDFLGYTSSNQAKSIIQKAGYIALYDNEFSSKKPSGKIIVAGSSSITPLMEKLKESYKSLNPKATIEIQQSDSTTGINSAIEKIADIAMVSREFKDSELKNGLKTQVLALDGLAVIVNKANPIDSLSKDSVKKIFTGDITTWEKVK
>NZ_CP018788.1|WP_086302995.1|1414132_1415440_+|MFS-transporter
MIRSVLPLGFIAASRFFGLFIILPVLSLYALELDGANEFLAGLTIGAYAITQMIFQLPFGSLSDRFGRKFMIFVGLIIFIIGSLICAISTDIYTMLFGRLLQGCGAVGAVATAMISDLVSEDKRSKAMAMMGGMIGIAFAISMILSPLLSREFGLSSLFYLSIIVTIFCIFLLFSAVPKEPKIHHHDPKIPLTKLLKQKDLAIMNLTNLMQKMLMSCAFVAIPIVLVKSLEYSTDNLWIVYLISMIFGFLAMGMAGFLGDGKGHSKKLLLIGVVLFIISFIGFGVANSAVSFIIFVVIFFIGFNIHEPIMQSCASKFAKSNQRGSALGIFNSFGYLGSFLGGAVGGYLLHSYNITALAVVLAVASAIWLLILFQLSDPRIFQIIRLKNADISILDSVNGIVDRYKQNGYSIVKFNSNIISRDEVISILGVSNEEL
>NZ_CP018788.1|WP_086302997.1|1415426_1416611_+|molybdopterin-molybdotransferase-MoeA
MKSYNENLQNLLNLAPKWDFIERVSLDRALGRILADDIVAKSPYPAYPTSSMDGYAIKFTNQNNKIKIINIAPAGNSDDIAISENECVKTLTGALVCDGADTIVPIENVKLSGEYIEITRPVSQGFAIREVGESYKESELLLSSRTKLGYCELALLAELGYSYINVLARPRVAILSTGSEVLDIGQIKEHKAQIYSSNSISISSLLKDMGCEPIIMPIIKDDKQAIQTALQNALISADFIITTGGVSVGDFDFMRDITRESKIIIDGASIKPGRHIKVAKINDKFIFALPGFAYSAMVTCVLFFKEFIEHIFGLNKKNRFKAILKDNHTKKSPFEEFSAASITNENGTIKISTATKKSGSSAIVGNLINGGVLLICPSDKDGLKAGEIVEYIEI
>NZ_CP018788.1|WP_086302999.1|1416607_1417291_-|hypothetical-protein
MKILSLASKLSLQSPKLVDKFKNDEIMVISPLDDSINANFIKCEIGAISYALALIGLEFGFGGEFWDELDCGELSGESNIGEEELPSICEFIKNCDICVISDEIFESNESSVKAILSLFKGKFGFKIVNLNGDEVELNGELVELEAIPSYDSAVVFTHPHCDEFRAGNYFGIAAKLKDGDEINIHLRQKDIKAKLSIDKSIKGTIGFLGFEGAKYGFEVLKFSPLVG
>NZ_CP018788.1|WP_086234974.1|1417691_1418048_+|hypothetical-protein
MDINSQISLNNLEIKPSDLELLGDYFSIIHHTPGRIRLRASLKLKNAAQNSDINPKDLMDKLSQLPLIKEIKFNKLIGSLTISYDPKLLEPSLFEDAANGRNLDKVASVINEILKDIK

Crispr_ID: NZ_CP018788_5

• CRISPR_ID: NZ_CP018788_5
• CRISPR_location: 1466746-1467145
• CRISPR_type: TypeII
• Repeat_type: NA
• Spacer_info: 5 spacers
• Cas_protein_info: cas4,cas2,cas1,cas9

Consensus repeat of NZ_CP018788_5

Consensus_repeat	Method
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	CRISPRCasFinder
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	CRT
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	PILER-CR

spacers of NZ_CP018788_5

>5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT
CTTCAAGAAAAAGATAAAGGCAAAAAAGGTGAAAA
>5.2|1466855|36|NZ_CP018788|CRISPRCasFinder,CRT
TATGGAACAAGTATTAAAACAATTTACTATCGCATT
>5.3|1466928|36|NZ_CP018788|CRISPRCasFinder,CRT
ATGTTTAAATATTTGAAGCTTTGCTAACGATTTATC
>5.4|1467001|36|NZ_CP018788|CRISPRCasFinder,CRT
TTAATCCGCAATCTAAAGATGATTTTATTTATCAAA
>5.5|1467074|35|NZ_CP018788|CRISPRCasFinder,CRT
TATCAGTCTTAACCCTTTCATTTTTGCAAGGGTTA
>5.6|1466784|35|NZ_CP018788|PILER-CR
CTTCAAGAAAAAGATAAAGGCAAAAAAGGTGAAAA
>5.7|1466856|36|NZ_CP018788|PILER-CR
TATGGAACAAGTATTAAAACAATTTACTATCGCATT
>5.8|1466929|36|NZ_CP018788|PILER-CR
ATGTTTAAATATTTGAAGCTTTGCTAACGATTTATC
>5.9|1467002|36|NZ_CP018788|PILER-CR
TTAATCCGCAATCTAAAGATGATTTTATTTATCAAA
>5.10|1467075|35|NZ_CP018788|PILER-CR
TATCAGTCTTAACCCTTTCATTTTTGCAAGGGTTA

CRISPR arrays and Neighbor proteins around NZ_CP018788_5

CRISPR arrays

The CRISPR arrays of NZ_CP018788_5

>merge|NZ_CP018788|5|1466746-1467145|CRISPRCasFinder,CRT,PILER-CR
ATTTTAAGCTGAGTTGATTTGTGGTATAATTTACAACCTTCAAGAAAAAGATAAAGGCAAAAAAGGTGAAAAGTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACTATGGAACAAGTATTAAAACAATTTACTATCGCATTGTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACATGTTTAAATATTTGAAGCTTTGCTAACGATTTATCGTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACTTAATCCGCAATCTAAAGATGATTTTATTTATCAAAGTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACTATCAGTCTTAACCCTTTCATTTTTGCAAGGGTTAGTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC

>NZ_CP018788|5|5|1466746-1467145|CRISPRCasFinder
ATTTTAAGCTGAGTTGATTTGTGGTATAATTTACAAC	CTTCAAGAAAAAGATAAAGGCAAAAAAGGTGAAAA
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	TATGGAACAAGTATTAAAACAATTTACTATCGCATT
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	ATGTTTAAATATTTGAAGCTTTGCTAACGATTTATC
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	TTAATCCGCAATCTAAAGATGATTTTATTTATCAAA
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	TATCAGTCTTAACCCTTTCATTTTTGCAAGGGTTA
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC

>NZ_CP018788|5|1|1466746-1467145|CRT
ATTTTAAGCTGAGTTGATTTGTGGTATAATTTACAAC	CTTCAAGAAAAAGATAAAGGCAAAAAAGGTGAAAA
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	TATGGAACAAGTATTAAAACAATTTACTATCGCATT
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	ATGTTTAAATATTTGAAGCTTTGCTAACGATTTATC
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	TTAATCCGCAATCTAAAGATGATTTTATTTATCAAA
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC	TATCAGTCTTAACCCTTTCATTTTTGCAAGGGTTA
GTTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC

>NZ_CP018788|5|1|1466747-1467145|PILER-CR
TTTTAAGCTGAGTTGATTTGTGGTATAATTTACAACC	TTCAAGAAAAAGATAAAGGCAAAAAAGGTGAAAAG
TTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACT	ATGGAACAAGTATTAAAACAATTTACTATCGCATTG
TTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACA	TGTTTAAATATTTGAAGCTTTGCTAACGATTTATCG
TTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACT	TAATCCGCAATCTAAAGATGATTTTATTTATCAAAG
TTTCAAACCGAGTTGATTTGTGGTATAATTTGCAACT	ATCAGTCTTAACCCTTTCATTTTTGCAAGGGTTAG
TTTCAAACCGAGTTGATTTGTGGTATAATTTGCAAC

Neighbor Proteins Overview

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP018788.1|WP_086246094.1|1465336_1466674_+|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	unknown	unknown	gnl|CDD|236269
NZ_CP018788.1|WP_086303059.1|1475153_1476362_+|phosphoglycerate-kinase	unknown	unknown	gnl|CDD|234613
NZ_CP018788.1|WP_086239172.1|1464208_1464769_-|dCTP-deaminase	unknown	unknown	gnl|CDD|234753
NZ_CP018788.1|WP_086303048.1|1468315_1469152_-|CRISPR-associated-endonuclease-Cas1	cas1	pfam01867_cas1_CAS-I:CAS-II:CAS-III	gnl|CDD|376633
NZ_CP018788.1|WP_086303046.1|1463071_1464199_-|UDP-4-amino-4,-6-dideoxy-N-acetyl-beta-L-altrosamine-transaminase	unknown	unknown	gnl|CDD|274662
NZ_CP018788.1|WP_086280460.1|1461347_1462943_+|arginine--tRNA-ligase	unknown	unknown	gnl|CDD|234964
NZ_CP018788.1|WP_086303054.1|1471287_1472967_-|hypothetical-protein	cas9	cd09704_cas9_CAS-II-B	gnl|CDD|274401
NZ_CP018788.1|WP_086225621.1|1460486_1461098_+|guanylate-kinase	unknown	unknown	gnl|CDD|234719
NZ_CP018788.1|WP_086253751.1|1464890_1465340_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	unknown	unknown	gnl|CDD|235777
NZ_CP018788.1|WP_086303044.1|1458060_1460487_+|hypothetical-protein	unknown	unknown	gnl|CDD|227596
NZ_CP018788.1|WP_086282656.1|1473235_1473562_-|ribosome-silencing-factor	unknown	unknown	gnl|CDD|272901
NZ_CP018788.1|WP_086303055.1|1473551_1474100_-|nicotinate-(nicotinamide)-nucleotide-adenylyltransferase	unknown	unknown	gnl|CDD|185680
NZ_CP018788.1|WP_086225670.1|1467357_1467924_-|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	gnl|CDD|273040
NZ_CP018788.1|WP_086225671.1|1467924_1468194_-|CRISPR-associated-endonuclease-Cas2	cas2	pfam09827_cas2_CAS-I:CAS-II:CAS-III	gnl|CDD|378256
NZ_CP018788.1|WP_086225619.1|1457226_1458000_+|flagellar-type-III-secretion-system-protein-FliR	unknown	unknown	gnl|CDD|235568
NZ_CP018788.1|WP_086225622.1|1461135_1461348_+|twin-arginine-translocase-TatA/TatE-family-subunit	unknown	unknown	gnl|CDD|234822
NZ_CP018788.1|WP_086303050.1|1469132_1469678_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086303042.1|1456385_1456667_-|hypothetical-protein	unknown	unknown	unknown
NZ_CP018788.1|WP_086303057.1|1474156_1475152_+|type-I-glyceraldehyde-3-phosphate-dehydrogenase	unknown	unknown	gnl|CDD|223135
NZ_CP018788.1|WP_143297692.1|1469794_1471180_-|hypothetical-protein	unknown	unknown	gnl|CDD|379160

HMMScan for Signature genes

Protein	Cas_name	Cas_description	E-value	Identity	Coverage
NZ_CP018788.1|WP_086303054.1|1471287_1472967_-|hypothetical-protein	cas9	cd09704_cas9_CAS-II-B	1.2e-36	121.0	47.5
NZ_CP018788.1|WP_086303048.1|1468315_1469152_-|CRISPR-associated-endonuclease-Cas1	cas1	pfam01867_cas1_CAS-I:CAS-II:CAS-III	2.1e-60	199.2	6.5
NZ_CP018788.1|WP_086225670.1|1467357_1467924_-|CRISPR-associated-protein-Cas4	cas4	cd09637_cas4_CAS-I:CAS-II:CAS-V	1e-21	72.6	0.7
NZ_CP018788.1|WP_086225671.1|1467924_1468194_-|CRISPR-associated-endonuclease-Cas2	cas2	pfam09827_cas2_CAS-I:CAS-II:CAS-III	2.9e-17	57.6	0.3

rpsblast for functional proteins

Protein	Function_ID	Function_description	E-value
NZ_CP018788.1|WP_086246094.1|1465336_1466674_+|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	gnl|CDD|236269	PRK08462, PRK08462, acetyl-CoA carboxylase biotin carboxylase subunit.	0
NZ_CP018788.1|WP_086303059.1|1475153_1476362_+|phosphoglycerate-kinase	gnl|CDD|234613	PRK00073, pgk, phosphoglycerate kinase; Provisional.	0
NZ_CP018788.1|WP_086239172.1|1464208_1464769_-|dCTP-deaminase	gnl|CDD|234753	PRK00416, dcd, deoxycytidine triphosphate deaminase; Reviewed.	2.93506e-103
NZ_CP018788.1|WP_086303048.1|1468315_1469152_-|CRISPR-associated-endonuclease-Cas1	gnl|CDD|376633	pfam01867, Cas_Cas1, CRISPR associated protein Cas1. Clustered regularly interspaced short palindromic repeats (CRISPRs) are a family of DNA direct repeats found in many prokaryotic genomes. This family of proteins corresponds to Cas1, a CRISPR-associated protein. Cas1 may be involved in linking DNA segments to CRISPR.	5.03366e-61
NZ_CP018788.1|WP_086303046.1|1463071_1464199_-|UDP-4-amino-4,-6-dideoxy-N-acetyl-beta-L-altrosamine-transaminase	gnl|CDD|274662	TIGR03588, PseC, UDP-4-amino-4,6-dideoxy-N-acetyl-beta-L-altrosamine transaminase. This family of enzymes are aminotransferases of the pfam01041 family involved in the biosynthesis of pseudaminic acid. They convert UDP-4-keto-6-deoxy-N-acetylglucosamine into UDP-4-amino-4,6-dideoxy-N-acetylgalactose. Pseudaminic acid has a role in surface polysaccharide in Pseudomonas as well as in the modification of flagellin in Campylobacter and Helicobacter species.	1.85591e-178
NZ_CP018788.1|WP_086280460.1|1461347_1462943_+|arginine--tRNA-ligase	gnl|CDD|234964	PRK01611, argS, arginyl-tRNA synthetase; Reviewed.	1.54027e-166
NZ_CP018788.1|WP_086303054.1|1471287_1472967_-|hypothetical-protein	gnl|CDD|274401	TIGR03031, cas_csx12, CRISPR system subtype II-B RNA-guided endonuclease Cas9/Csx12. Members of this family of CRISPR-associated (cas) protein are found, so far, in CRISPR/cas loci in Wolinella succinogenes DSM 1740, Legionella pneumophila str. Paris, and Francisella tularensis, where the last probably is an example of a degenerate CRISPR locus, having neither repeats nor a functional Cas1. The characteristic repeat length is 37 base pairs and period is about 72. One region of this large protein shows sequence similarity to pfam01844, HNH endonuclease.	9.16572e-33
NZ_CP018788.1|WP_086225621.1|1460486_1461098_+|guanylate-kinase	gnl|CDD|234719	PRK00300, gmk, guanylate kinase; Provisional.	5.51204e-98
NZ_CP018788.1|WP_086282656.1|1473235_1473562_-|ribosome-silencing-factor	gnl|CDD|272901	TIGR00090, rsfS_iojap_ybeB, ribosome silencing factor RsfS/YbeB/iojap. This model describes a widely distributed family of bacterial proteins related to iojap from plants. It includes RsfS(YbeB) from E. coli. The gene iojap is a pattern-striping gene in maize, reflecting a chloroplast development defect in some cells. The conserved function of this protein is to silence ribosomes by binding the ribosomal large subunit and impairing joining with the small subunit in response to nutrient stress. Note that RsfS (starvation) is an author-endorsed change from the published symbol RsfA, which conflicted with previously published gene symbols. [Protein synthesis, Translation factors].	2.52766e-34
NZ_CP018788.1|WP_086303044.1|1458060_1460487_+|hypothetical-protein	gnl|CDD|227596	COG5271, MDN1, AAA ATPase containing von Willebrand factor type A (vWA) domain [General function prediction only].	6.99212e-06
NZ_CP018788.1|WP_086303055.1|1473551_1474100_-|nicotinate-(nicotinamide)-nucleotide-adenylyltransferase	gnl|CDD|185680	cd02165, NMNAT, Nicotinamide/nicotinate mononucleotide adenylyltransferase. Nicotinamide/nicotinate mononucleotide (NMN/ NaMN)adenylyltransferase (NMNAT). NMNAT represents the primary bacterial and eukaryotic adenylyltransferases for nicotinamide-nucleotide and for the deamido form, nicotinate nucleotide. It is an indispensable enzyme in the biosynthesis of NAD(+) and NADP(+). Nicotinamide-nucleotide adenylyltransferase synthesizes NAD via the salvage pathway, while nicotinate-nucleotide adenylyltransferase synthesizes the immediate precursor of NAD via the de novo pathway. Human NMNAT displays unique dual substrate specificity toward both NMN and NaMN, and can participate in both de novo and salvage pathways of NAD synthesis.	3.30816e-48
NZ_CP018788.1|WP_086225670.1|1467357_1467924_-|CRISPR-associated-protein-Cas4	gnl|CDD|273040	TIGR00372, conserved_hypothetical_protein, CRISPR-associated protein Cas4. This model represents a family of proteins associated with CRISPR repeats in a wide set of prokaryotic genomes. This scope of this model has been broadened since it was first built to describe an archaeal subset only. The function of the protein is undefined. Distantly related proteins, excluded from this model, include ORFs from Mycobacteriophage D29 and Sulfolobus islandicus filamentous virus and a region of the Schizosaccharomyces pombe DNA replication helicase Dna2p.	2.39886e-14
NZ_CP018788.1|WP_086225671.1|1467924_1468194_-|CRISPR-associated-endonuclease-Cas2	gnl|CDD|378256	pfam09827, CRISPR_Cas2, CRISPR associated protein Cas2. Members of this family of bacterial proteins comprise various hypothetical proteins, as well as CRISPR (clustered regularly interspaced short palindromic repeats) associated proteins, conferring resistance to infection by certain bacteriophages.	1.0476e-09
NZ_CP018788.1|WP_086225619.1|1457226_1458000_+|flagellar-type-III-secretion-system-protein-FliR	gnl|CDD|235568	PRK05701, fliR, flagellar type III secretion system protein FliR.	1.48269e-59
NZ_CP018788.1|WP_086225622.1|1461135_1461348_+|twin-arginine-translocase-TatA/TatE-family-subunit	gnl|CDD|234822	PRK00720, tatA, twin-arginine translocase TatA/TatE family subunit.	2.77267e-18
NZ_CP018788.1|WP_086253751.1|1464890_1465340_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein	gnl|CDD|235777	PRK06302, PRK06302, acetyl-CoA carboxylase biotin carboxyl carrier protein.	9.20816e-49
NZ_CP018788.1|WP_086303057.1|1474156_1475152_+|type-I-glyceraldehyde-3-phosphate-dehydrogenase	gnl|CDD|223135	COG0057, GapA, Glyceraldehyde-3-phosphate dehydrogenase/erythrose-4-phosphate dehydrogenase [Carbohydrate transport and metabolism].	1.2401e-158
NZ_CP018788.1|WP_143297692.1|1469794_1471180_-|hypothetical-protein	gnl|CDD|379160	pfam13395, HNH_4, HNH endonuclease. This HNH nuclease domain is found in CRISPR-related proteins.	5.35384e-08

Protein sequences

>NZ_CP018788.1|WP_086246094.1|1465336_1466674_+|acetyl-CoA-carboxylase-biotin-carboxylase-subunit
MREIKRILIANRGEIALRALRTIQEMGKEAVVVHSTADKDALYVKYADASICIGGARSSESYLHIPAIITACEISEADAIFPGYGFLSENQNFVEICEKHNIKFIGPSVEAMALMSDKSKAKQMMMRAGIPVVPGSDGAIKDMEMAKKLASEIGYPVIIKAAAGGGGRGMRVVEKEEDLEKSFWSAESEAMSAFGDGTMYMEKYISNPRHIEVQVLGDEYGNVIHVGERDCSMQRRHQKLIEESPAVILDDETRAQLHQTAVNAAKAIGYTGAGTFEFLYDQRDNKFYFIEMNTRLQVEHCVSEMCSGLDLIEWMIRISQGERLPEQKDIKLSGHSIECRITAEDPKSFTPNPGKITKYVAPGGRNVRMDSHVYEGYSVPPYYDSMIGKLIVHDIDRNRAIAKMKVALDELIIQGIKTTKDFHINMMNNDDFINNLYDTNYLAKH
>NZ_CP018788.1|WP_086253751.1|1464890_1465340_+|acetyl-CoA-carboxylase-biotin-carboxyl-carrier-protein
MTRDEIKELMSFFDETNINKIKIKDGDFVIELEKHEPCEQIAPAPACPTIPAPAPINVVVNEKTVTTSTATDTLNAPMVGTFYIAPSPGAPSFVKVGQTVKKGDTIGIIEAMKIMNEIEAEFDCRITKALIADGQPVEFGMALFEVEKL
>NZ_CP018788.1|WP_086239172.1|1464208_1464769_-|dCTP-deaminase
MGLKSDKWIRQMSLEHKMITPFCEENIGRGVVSYGLSSYGYDIRVGNEFKIFTNVGGTVVDPKNFDEKNVVDFIGDICIVPPNSFALARTVEYFIMPRDTLAICLGKSTYARCGIIVNVTPFEPGFEGHITIEISNTTPLPAKIYANEGIAQVLFLQGDEICETSYADKNGKYQSQTGITLPRILQ
>NZ_CP018788.1|WP_086303046.1|1463071_1464199_-|UDP-4-amino-4,-6-dideoxy-N-acetyl-beta-L-altrosamine-transaminase
MMVYSRQKIEDDDIQAVVEALKSDMLTCGNRVVDFESALCELTGAKYAVVMNSATSALHAGYIALGVGPGDEVITTPITFAATANAAIMCGARIKFADVLLNGNINPASIKELISDKTKVITAVDFGGYPVDMDAIKALIKEQDIKIIDDASHALGSSINGKMVGTLADATIFSFHAIKPITTFEGGALLTNDENIAKSARLTRSHGMVKKQAWNMDMVTLGYNYRLSDVACALGLSQIKKLDKFINRRYEIAKIYDDAFKNSKYLKTIDIPDNIRSARHLYPVLLNSNLWCVKEDIYNELHAMGIGVQVHYKPTYQFSFYKNLYGEMRLDGAEDFYRAELSLPCHQMMSDDDAKFVIANLNELLEIYTSKSVCG
>NZ_CP018788.1|WP_086280460.1|1461347_1462943_+|arginine--tRNA-ligase
MSAKDTLKNEISAILGREVVIEKPKDKTLAHYATPLAFGLAKELKKSPVAIAAQMAQQFSSPNYEVTAVNGYINFKLSGDFLDSLANDALKSGDKFGSKEITNPKNIFLEYISANPTGPLHIGHVRGAVYGDTLARVARHIGVGVHTEYYINDAGNQIDLLGISITLRAKEILFNETVEYPEKYYRGDYIDELAHKAYDKFGKEIFESSRNSELAEFAKDEVLKIIKKDLADAGIFIDNWASEKSYYDQLEQTLEQLEKSGQVYKKDSTTYIASSKLGDDSDRVVVRSDGRPTYLAGDIIYHNVKFANDFDTYINIWGADHHGYIARLKAAINFLGYDESKLEVILMQMVSLLKDGKPFKMSKRAGTSVLMSDILAEIGSDALRFIFISKAGNSSLEFDIDELKKQDSSNPIFYINYAHARVNQIFAKANKTPADVANASLTNLSDDGKNLLFEALTMPEVLEDALNQRSLHKIPDYLKSLSASFHKFYNENRVVGSQNEDELLKLFSVVALSIKVALNLMGIKAKDIMEN
>NZ_CP018788.1|WP_086225622.1|1461135_1461348_+|twin-arginine-translocase-TatA/TatE-family-subunit
MGSMSISHWLIVLAIIVLLFGAKKIPELAKGMGKGIKSFKKEMEDDTSLEKIEKTEDTTQIKKDETQKSA
>NZ_CP018788.1|WP_086225621.1|1460486_1461098_+|guanylate-kinase
MSGQILIISGPSGSGKSTLLSRLMAEFDNLYFSISSTTREPRAGEKNGVDYNFISTDEFKQGIEQGKFLEWANVHKNYYGTSLEPVEKALKDDKIVIFDIDVQGFHLAMKQYKELITSVFITTKDRLELKKRLIKRGSDDEQTIENRLFNAATEIAHIGEYDYLIINDDLDSSYEKLKAIFISMRSKTQSFIINDVIESWSEC
>NZ_CP018788.1|WP_086303044.1|1458060_1460487_+|hypothetical-protein
MKVILLNNNPAVSKLVSVSLNKLGYTFAEIDNLEYLTSNDADLIICDSGLYDSKINYLEYAKNQLFLIPRNRADEYNLAKSQTLQKPFLPTDFIDVVKRILVEIPKSTKIVEPKPSDIKVGDEFGQIHTNDKIDVFSDLNSDELLDDVNKLQDDFENSSFDDENHEEQELEQFENLIEVAEPELAKDEFDDDLGLDDESGKIESLMDKSKDVNNLTDDLMSDNKELNIATDEFNLDNIDDELAKLDNLEYETDNLADKNLNKSVDESQAKSVDNQINANNQIQELDDADLDLDNPGIKLNKIDSLDDKKELDTLDNTDNLADKNLNKSVDESQAKSVDNQINANNQIQELDDADLDLDNPGIKLNEIDSLDDKKELDTLDNTDNLADKNLNKSVDESQAKSVDNQINANNQIQELDDADLDLDNPGIKLNEIDSLDDKKELDTLDNKASEIEALDDLSNDEQIIDNLDNQAQESSPSNELNDEQKQQNIKDITSEYENIKLDISALDALPDGDGEVDNAEFDTTFKDEIKDESAIKPVGKPELESKFQDDSVADLAAIPQEITECDEIDKESIIQPETVAKFATDEFEQTQPVQESKSEFEFKDKSIDESTQKTKPAFLVEEIGLDKSDNELDDLESELAGFENDLANIKSSQDDEPLDFDESQDFNELADENDQVKDVEYTENLNKLSSMLDEIDNMDCENNMKNQDLSNSYEASTIDEIEEAAIKEALHEENNKEDSQTQNEPKVNQSDKNAVENKTEPSQNEQKEIAQVLASQIGEGLGRAFSTSALKDVLKDINININISFEGR
>NZ_CP018788.1|WP_086225619.1|1457226_1458000_+|flagellar-type-III-secretion-system-protein-FliR
MEFVNYLGQENVVTFFLLLVRTGALMVFFPFFNHMQIPMTIKATLSFMLTLYLFPLATPPANLDGINVQYLILEALSELMLGLCVGVLLMLVFGAVQLAGEQISMIMGFSMATVIDPQSGINAPLISNILNLIVLLAFLLFDGHHLVLYFLAYGLEYIPLGGFYPEQNILKYASQGMVNLFLYGFIISFPILALTLMSDLIFGMLMKTMPQFNLLVVGFPIKITIAFVVLMAILAVIVKVFTTLMMRVLNDLPSLFF
>NZ_CP018788.1|WP_086303042.1|1456385_1456667_-|hypothetical-protein
MGFFSTIEAAIQQAEQTRQQSQSNIISAIGTAISQVSAQVEAEENEIKAKRQELLNAMIGCKEMMAKTPQSLADRKIELSKKQNSNDDEYITL
>NZ_CP018788.1|WP_086225670.1|1467357_1467924_-|CRISPR-associated-protein-Cas4
MILVSHIRQFVFCPRILYFYTFCDIKPVYPEYVSSGSQYHNKQNELFKNRKFIKFKLPIIKAYSNLYLQDSSMQGVADLVLECQNEIIVAEFKNQNKPILNKGTKMQLIAYSKLASKHFNKPFFKIMLICSNNLKFKIFDINSDDLAQFNSTIDKINKMLNQELFPQSCASIAACMQCEFKNYCDDRE
>NZ_CP018788.1|WP_086225671.1|1467924_1468194_-|CRISPR-associated-endonuclease-Cas2
MRYLICYDIENSKNRTKLFERLKDFGLLAVQKSVFYGELSRADKLAIKELLSKYCAKSDKAIIASVNLDFNDTLGYTKECFESKIYEII
>NZ_CP018788.1|WP_086303048.1|1468315_1469152_-|CRISPR-associated-endonuclease-Cas1
MKHLVINSFGLFLGLKSQRIVIYQNKEIIKEIALKSLKTISINSNGITISSDLIFACSVRGIKIFYQNFNTFSATHTLYEHKGVNVLKQQFSSKDNAKGLMLAKELIIGKIKNQRSTILYFSRNKNNEQKNTALIAMQKAIDTLKSSKIIDTNDIFSIEANAAHRYFEFLKFNSLLPSSFEHRTKRASSEISNQALNYGYAILLNIIYKSIINAGLNPYFGVLHTMRSAKPSLALDIMEEYRSFIVDRNIIKIRSSLKGELNAELKKSNSFKYIKFIK
>NZ_CP018788.1|WP_086303050.1|1469132_1469678_-|hypothetical-protein
MPIKAIKSPNYIIRQNGGYAGLVNSDIATKTYIDLDSKNIIKIPFFSKNILPRKIADIINIIELKSKNIKQIYKLLVTKNLPSAIIKLEYIISQANRHDIEVEFDKSQIGDYNLLDQTSRDEFIDKYLNGEFKELLGKPRDNKITIIKDTKDSLIITYCTQTSAIHKKIMLDNLIDETSSY
>NZ_CP018788.1|WP_143297692.1|1469794_1471180_-|hypothetical-protein
MPANSARLINGKIEMYLNRLAYEISTAIKPEILKDISYITINVEMNKFSFENSASDLNLISKRQKSKDMICPYSGQKIDEINCEYDHILPRSKGLYNSRANLIPASSTANLQKGNQSYTLENLHQNYLNSIYKIIKVQNLDEFKNFIDTQMAKININKFTNFDNLNSIEQIALRHALFYKNSDSFTKALEILKLDRIKTHSNGTQKRFVNLLIQKVKDKLNKSNQDIEFSVNFINAELVSAIRSELSKEDKELQKAKIQDSHSHCIDASIVFYYANSKLIKNSKGQREFKYNYNHIKPEYSNKMTMQSKKYLELNSNKISRKKLFDDGVYSLVYENANILKDKEANILLDLGLLHTKENGKKVAITSDFKSGKFYISTHKVFDLLFKAFNEGDIKLLNKLKFLDNHLCSYIRKDIFAIIKDEDKSSMFFNNKNELKVPDAKIKTKNIDKFYHILKQMKARL
>NZ_CP018788.1|WP_086303054.1|1471287_1472967_-|hypothetical-protein
MYELSINVDMGAANNGVFIAITNENSIIYKNAFNIYFDKNLTFSKSDRTARRHARRSYDRDRFILRLLNEILPIDGLSQSQIETIYGLFKNRGFNYHNIEFNESLDDDVVEFLNGLDRYIFGLSKNKDEFEQIINEIVVDHSNDEIKKILDTQSQILINIDKENKKAIKASKNIQSLIQSICNEIDKNNKHRISYLKDIKELIYKDCEFIIQKSDKFDNLDEFYNFVGNISNFQTRILRRYFNNKYLDNINFDDAKLKKNIIRNINYMEYITDIQNNNKLNMLNSLKTKSALEYLKSIDPVITIPPYENRKNKNPQKCNTLMLNIDKITPSLANLTYKILNSDDFTHIRRDENGQLISLNDINENNIAKYLQRVLDISKESLIDVALYPRALDNNSKIFADTFRLNSDEIREFKEFARRYYNEVDNAKKGIITNDLLIPCGKNTPHKNRNKNELISALFGKNITKDDVINLEEFMLKNKIKGNRSYKGFFRDLNELKKSYQNSFYHNLNNDEINDKDIQTILELYPKVAQNINNHNSVFEFKHPFDKNNLIQISTILAS
>NZ_CP018788.1|WP_086282656.1|1473235_1473562_-|ribosome-silencing-factor
MQNRIDRIVKLLDEKKAENIEVIDMQGRDYLSKFVVVATTLAARHGAALLDDLKTELKPAGENFLGVESSDDWTVIDLGDIMIHLMSETYRAKYNIEEFLKELSVKGN
>NZ_CP018788.1|WP_086303055.1|1473551_1474100_-|nicotinate-(nicotinamide)-nucleotide-adenylyltransferase
MNIAIFGGSFDPPHLGHDMIVKEVLKSLNINKLIIIPTFLSPFKSEFGAPPLLRLQWCNELWSNLDEKIIISDYEISQNRPVATIESVSYFKNKFNASRIYLIIGADQLNSLHKWHRYDELKALVSFVVACRDGIKIDENLQKLDINVKISSSKIKSELNFKHIPTAILDSVEKFYKDKNAK
>NZ_CP018788.1|WP_086303057.1|1474156_1475152_+|type-I-glyceraldehyde-3-phosphate-dehydrogenase
MALKIAINGFGRIGRCAARIILNNPAEYELCIINDTAERKMTRYLLKYDTVHGEFNQDVEVLNDDYIAVNGKKIRVYSTRDINDLDLRGIDVVLECTGKFLTKEQCQTYIAKGAKKVIMSAPAKDDTPTFVLGVNSDKYEGQTIISNASCTTNCLGPVTRVLEDLYGIKKGLMTTIHAYTNGQSLVDVKCRDFRRSRAAAANMIPTSTGAAKAMKLVMPSLDGKLHGQSIRVPVPNVSIVDLTAVLEKSVTKDELNNAFVEASKGSLKGIMAVDFDERVSSDFITSNYSSIVAADLTQVICGDMIKVMAWYDNEWGYSNRLVEMAKFISEK
>NZ_CP018788.1|WP_086303059.1|1475153_1476362_+|phosphoglycerate-kinase
MSEIISIKDIEFKSGSKVLVRCDFNTPMDEFNNITDDRRIRSVIPTIRYILDQGCSVILASHLGRPKNGYEDKYSLLPVAKRLGRLMDREIKFAHDVVGHDAKEKVQKLQSGEILLLENLRFEKGETKDDINLAKSLSEFANYYINDAFGVCHRAHSSVHAITQCYDSEHKAAGFLLIKEIEFGQNLIRHPSRPFVAVTGGSKVSGKLQALTNLLPRIDKLIIGGGMAFTFLKALGENIGNSLLEEELVEEASNILKKGRELGVKIYLPVDVVAAQSFSNDSAIKYVPVQEIPNGWMGLDIGPASVKLFKEAIADAQTIWWNGPMGVFEMDKFSKGSIKMSHAIGESFATTVVGGGDTADVVERAGDTDEMTFISTGGGASLELIEGKELPGVRVLLREDDI

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP007000	Campylobacter fetus subsp. venerealis cfvi03/293 plasmid pCfviMP1, complete sequence	2673-2707	1	0.971
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP007000	Campylobacter fetus subsp. venerealis cfvi03/293 plasmid pCfviMP1, complete sequence	2673-2707	1	0.971
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NC_012040	Campylobacter lari RM2100 plasmid pCL2100, complete sequence	29843-29877	6	0.829
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP007767	Campylobacter peloridis LMG 23910 plasmid pPEL1, complete sequence	26143-26177	6	0.829
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NC_012040	Campylobacter lari RM2100 plasmid pCL2100, complete sequence	29843-29877	6	0.829
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP007767	Campylobacter peloridis LMG 23910 plasmid pPEL1, complete sequence	26143-26177	6	0.829
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_KX686749	Campylobacter coli strain Tx40 plasmid unnamed, complete sequence	38182-38216	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP028373	Campylobacter jejuni subsp. jejuni strain huA17 plasmid unnamed1, complete sequence	12079-12113	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP022078	Campylobacter jejuni strain FDAARGOS_265 plasmid unnamed1, complete sequence	22668-22702	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP007182	Campylobacter coli RM4661 plasmid pRM4661_48kbp, complete sequence	38320-38354	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017230	Campylobacter jejuni strain FORC_046 isolate Not reported plasmid pFORC46.1, complete sequence	43358-43392	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NC_006134	Campylobacter coli plasmid pCC31, complete sequence	41959-41993	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NC_006135	Campylobacter jejuni subsp. jejuni 81-176 plasmid pTet, complete sequence	42457-42491	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP007180	Campylobacter coli RM5611 plasmid pRM5611_48kb, complete sequence	42437-42471	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017869	Campylobacter coli strain MG1116 plasmid pCCDM116L, complete sequence	41960-41994	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP044166	Campylobacter coli strain AR-0416 plasmid pAR-0416	165914-165948	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP045046	Campylobacter jejuni subsp. jejuni strain NADC 20827 plasmid p20827L, complete sequence	40600-40634	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP010073	Campylobacter jejuni subsp. jejuni strain 01-1512 plasmid pCj1, complete sequence	30355-30389	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017857	Campylobacter jejuni strain YQ2210 plasmid pCJDM210L, complete sequence	42728-42762	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP023544	Campylobacter jejuni strain CFSAN032806 plasmid pCFSAN032806, complete sequence	40566-40600	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017854	Campylobacter jejuni strain ZP3204 plasmid pCJDM204L, complete sequence	25823-25857	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	CP002030	Campylobacter jejuni subsp. jejuni ICDCCJ07001 plasmid pTet, complete sequence	40718-40752	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP028186	Campylobacter jejuni strain CFSAN054107 plasmid pGMI16-002, complete sequence	59545-59579	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP022471	Campylobacter jejuni strain jejuni plasmid pRM1246_ERRC, complete sequence	38604-38638	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	CP013735	Campylobacter coli strain OR12 plasmid pOR12TET, complete sequence	25449-25483	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017418	Campylobacter jejuni strain MTVDSCj13 plasmid pMTVDSCj13-1, complete sequence	34383-34417	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017419	Campylobacter jejuni strain MTVDSCj16 plasmid pMTVDSCj16-1, complete sequence	34769-34803	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017866	Campylobacter coli strain YF2105 plasmid pCCDM105L, complete sequence	19596-19630	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017879	Campylobacter coli strain BG2108 plasmid pCCDM108L, complete sequence	29046-29080	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017416	Campylobacter jejuni strain MTVDSCj07 plasmid pMTVDSCj07-1, complete sequence	35353-35387	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017872	Campylobacter coli strain BP3183 plasmid pCCDM183, complete sequence	28672-28706	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP020775	Campylobacter jejuni strain YH002 plasmid pCJP002, complete sequence	43156-43190	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NC_022355	Campylobacter coli CVM N29710 plasmid pN29710-1, complete sequence	40532-40566	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_KJ646012	Campylobacter jejuni strain 11601MD plasmid p11601MD, complete sequence	18739-18773	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP045793	Campylobacter coli strain CFSAN032805 plasmid p1CFSAN032805, complete sequence	35170-35204	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NC_017282	Campylobacter jejuni subsp. jejuni S3 plasmid pTet, complete sequence	11347-11381	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	CP047483	Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence	15482-15516	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	CP047483	Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence	23832-23866	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP013035	Campylobacter coli strain HC2-48 plasmid pccdm1, complete sequence	28329-28363	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP007752	Campylobacter jejuni subsp. jejuni D42a plasmid pTet-D42a, complete sequence	32157-32191	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP014745	Campylobacter jejuni strain OD267 plasmid pCJDM67 L, complete sequence	50957-50991	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP023546	Campylobacter coli strain CFSAN032805 plasmid pCFSAN032805_1, complete sequence	35741-35775	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017026	Campylobacter coli plasmid pCC14983A-1, complete sequence	104755-104789	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP011017	Campylobacter coli strain FB1 plasmid pFB1TET, complete sequence	4030-4064	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017030	Campylobacter jejuni subsp. jejuni strain 14980A plasmid pCJ14980A, complete sequence	31921-31955	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP014743	Campylobacter jejuni strain WP2202 plasmid pCJDM202, complete sequence	52988-53022	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017877	Campylobacter coli strain ZV1224 plasmid pCCDM224L, complete sequence	20501-20535	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP044168	Campylobacter jejuni strain AR-0415 plasmid pAR-0415, complete sequence	39802-39836	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP040609	Campylobacter sp. CFSAN093226 plasmid unnamed, complete sequence	22800-22834	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP017861	Campylobacter jejuni strain TS1218 plasmid pCJDM218, complete sequence	32465-32499	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP043764	Campylobacter jejuni strain BfR-CA-14430 plasmid pBfR-CA-14430, complete sequence	9257-9291	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP007750	Campylobacter jejuni subsp. jejuni M129 plasmid pTet-M129, complete sequence	30407-30441	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP048762	Campylobacter jejuni strain ZS004 plasmid pCJFEX, complete sequence	44575-44609	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_CP044170	Campylobacter jejuni strain AR-0413 plasmid pAR-0413-1, complete sequence	66061-66095	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_MK541987	Campylobacter coli strain CVM N46788F plasmid pN46788F, complete sequence	583-617	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_MK541988	Campylobacter coli strain CVM N61740F plasmid pN61740F, complete sequence	35776-35810	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NZ_MK541989	Campylobacter coli strain CVM N61925F plasmid pN61925F, complete sequence	11512-11546	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NC_022354	Campylobacter jejuni subsp. jejuni 00-2544 plasmid unnamed, complete sequence	13142-13176	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_KX686749	Campylobacter coli strain Tx40 plasmid unnamed, complete sequence	38182-38216	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP028373	Campylobacter jejuni subsp. jejuni strain huA17 plasmid unnamed1, complete sequence	12079-12113	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP022078	Campylobacter jejuni strain FDAARGOS_265 plasmid unnamed1, complete sequence	22668-22702	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP007182	Campylobacter coli RM4661 plasmid pRM4661_48kbp, complete sequence	38320-38354	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017230	Campylobacter jejuni strain FORC_046 isolate Not reported plasmid pFORC46.1, complete sequence	43358-43392	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NC_006134	Campylobacter coli plasmid pCC31, complete sequence	41959-41993	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NC_006135	Campylobacter jejuni subsp. jejuni 81-176 plasmid pTet, complete sequence	42457-42491	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP007180	Campylobacter coli RM5611 plasmid pRM5611_48kb, complete sequence	42437-42471	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017869	Campylobacter coli strain MG1116 plasmid pCCDM116L, complete sequence	41960-41994	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP044166	Campylobacter coli strain AR-0416 plasmid pAR-0416	165914-165948	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP045046	Campylobacter jejuni subsp. jejuni strain NADC 20827 plasmid p20827L, complete sequence	40600-40634	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP010073	Campylobacter jejuni subsp. jejuni strain 01-1512 plasmid pCj1, complete sequence	30355-30389	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017857	Campylobacter jejuni strain YQ2210 plasmid pCJDM210L, complete sequence	42728-42762	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP023544	Campylobacter jejuni strain CFSAN032806 plasmid pCFSAN032806, complete sequence	40566-40600	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017854	Campylobacter jejuni strain ZP3204 plasmid pCJDM204L, complete sequence	25823-25857	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	CP002030	Campylobacter jejuni subsp. jejuni ICDCCJ07001 plasmid pTet, complete sequence	40718-40752	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP028186	Campylobacter jejuni strain CFSAN054107 plasmid pGMI16-002, complete sequence	59545-59579	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP022471	Campylobacter jejuni strain jejuni plasmid pRM1246_ERRC, complete sequence	38604-38638	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	CP013735	Campylobacter coli strain OR12 plasmid pOR12TET, complete sequence	25449-25483	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017418	Campylobacter jejuni strain MTVDSCj13 plasmid pMTVDSCj13-1, complete sequence	34383-34417	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017419	Campylobacter jejuni strain MTVDSCj16 plasmid pMTVDSCj16-1, complete sequence	34769-34803	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017866	Campylobacter coli strain YF2105 plasmid pCCDM105L, complete sequence	19596-19630	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017879	Campylobacter coli strain BG2108 plasmid pCCDM108L, complete sequence	29046-29080	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017416	Campylobacter jejuni strain MTVDSCj07 plasmid pMTVDSCj07-1, complete sequence	35353-35387	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017872	Campylobacter coli strain BP3183 plasmid pCCDM183, complete sequence	28672-28706	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP020775	Campylobacter jejuni strain YH002 plasmid pCJP002, complete sequence	43156-43190	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NC_022355	Campylobacter coli CVM N29710 plasmid pN29710-1, complete sequence	40532-40566	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_KJ646012	Campylobacter jejuni strain 11601MD plasmid p11601MD, complete sequence	18739-18773	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP045793	Campylobacter coli strain CFSAN032805 plasmid p1CFSAN032805, complete sequence	35170-35204	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NC_017282	Campylobacter jejuni subsp. jejuni S3 plasmid pTet, complete sequence	11347-11381	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	CP047483	Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence	15482-15516	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	CP047483	Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence	23832-23866	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP013035	Campylobacter coli strain HC2-48 plasmid pccdm1, complete sequence	28329-28363	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP007752	Campylobacter jejuni subsp. jejuni D42a plasmid pTet-D42a, complete sequence	32157-32191	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP014745	Campylobacter jejuni strain OD267 plasmid pCJDM67 L, complete sequence	50957-50991	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP023546	Campylobacter coli strain CFSAN032805 plasmid pCFSAN032805_1, complete sequence	35741-35775	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017026	Campylobacter coli plasmid pCC14983A-1, complete sequence	104755-104789	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP011017	Campylobacter coli strain FB1 plasmid pFB1TET, complete sequence	4030-4064	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017030	Campylobacter jejuni subsp. jejuni strain 14980A plasmid pCJ14980A, complete sequence	31921-31955	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP014743	Campylobacter jejuni strain WP2202 plasmid pCJDM202, complete sequence	52988-53022	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017877	Campylobacter coli strain ZV1224 plasmid pCCDM224L, complete sequence	20501-20535	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP044168	Campylobacter jejuni strain AR-0415 plasmid pAR-0415, complete sequence	39802-39836	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP040609	Campylobacter sp. CFSAN093226 plasmid unnamed, complete sequence	22800-22834	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP017861	Campylobacter jejuni strain TS1218 plasmid pCJDM218, complete sequence	32465-32499	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP043764	Campylobacter jejuni strain BfR-CA-14430 plasmid pBfR-CA-14430, complete sequence	9257-9291	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP007750	Campylobacter jejuni subsp. jejuni M129 plasmid pTet-M129, complete sequence	30407-30441	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP048762	Campylobacter jejuni strain ZS004 plasmid pCJFEX, complete sequence	44575-44609	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_CP044170	Campylobacter jejuni strain AR-0413 plasmid pAR-0413-1, complete sequence	66061-66095	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_MK541987	Campylobacter coli strain CVM N46788F plasmid pN46788F, complete sequence	583-617	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_MK541988	Campylobacter coli strain CVM N61740F plasmid pN61740F, complete sequence	35776-35810	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NZ_MK541989	Campylobacter coli strain CVM N61925F plasmid pN61925F, complete sequence	11512-11546	7	0.8
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NC_022354	Campylobacter jejuni subsp. jejuni 00-2544 plasmid unnamed, complete sequence	13142-13176	7	0.8
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	NC_004996	Streptococcus phage SM1, complete genome	13305-13339	11	0.686
NZ_CP018788_5	5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT	1466783-1466817	35	AY007505	Streptococcus mitis phage SM1,complete genome	13305-13339	11	0.686
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	NC_004996	Streptococcus phage SM1, complete genome	13305-13339	11	0.686
NZ_CP018788_5	5.6|1466784|35|NZ_CP018788|PILER-CR	1466784-1466818	35	AY007505	Streptococcus mitis phage SM1,complete genome	13305-13339	11	0.686

1. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP007000 (Campylobacter fetus subsp. venerealis cfvi03/293 plasmid pCfviMP1, complete sequence) position: , mismatch: 1, identity: 0.971

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
cttcaagaaaaagataaaggtaaaaaaggtgaaaa	Protospacer
********************.**************

2. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP007000 (Campylobacter fetus subsp. venerealis cfvi03/293 plasmid pCfviMP1, complete sequence) position: , mismatch: 1, identity: 0.971

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
cttcaagaaaaagataaaggtaaaaaaggtgaaaa	Protospacer
********************.**************

3. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NC_012040 (Campylobacter lari RM2100 plasmid pCL2100, complete sequence) position: , mismatch: 6, identity: 0.829

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaattgaaaaagataaagacaaaaaaggcgaaaa	Protospacer
**    *************.*********.*****

4. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP007767 (Campylobacter peloridis LMG 23910 plasmid pPEL1, complete sequence) position: , mismatch: 6, identity: 0.829

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaattgaaaaagataaagacaaaaaaggcgaaaa	Protospacer
**    *************.*********.*****

5. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NC_012040 (Campylobacter lari RM2100 plasmid pCL2100, complete sequence) position: , mismatch: 6, identity: 0.829

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaattgaaaaagataaagacaaaaaaggcgaaaa	Protospacer
**    *************.*********.*****

6. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP007767 (Campylobacter peloridis LMG 23910 plasmid pPEL1, complete sequence) position: , mismatch: 6, identity: 0.829

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaattgaaaaagataaagacaaaaaaggcgaaaa	Protospacer
**    *************.*********.*****

7. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_KX686749 (Campylobacter coli strain Tx40 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

8. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP028373 (Campylobacter jejuni subsp. jejuni strain huA17 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

9. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP022078 (Campylobacter jejuni strain FDAARGOS_265 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

10. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP007182 (Campylobacter coli RM4661 plasmid pRM4661_48kbp, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

11. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017230 (Campylobacter jejuni strain FORC_046 isolate Not reported plasmid pFORC46.1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

12. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NC_006134 (Campylobacter coli plasmid pCC31, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

13. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NC_006135 (Campylobacter jejuni subsp. jejuni 81-176 plasmid pTet, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

14. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP007180 (Campylobacter coli RM5611 plasmid pRM5611_48kb, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

15. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017869 (Campylobacter coli strain MG1116 plasmid pCCDM116L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

16. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP044166 (Campylobacter coli strain AR-0416 plasmid pAR-0416) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

17. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP045046 (Campylobacter jejuni subsp. jejuni strain NADC 20827 plasmid p20827L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

18. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP010073 (Campylobacter jejuni subsp. jejuni strain 01-1512 plasmid pCj1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

19. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017857 (Campylobacter jejuni strain YQ2210 plasmid pCJDM210L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

20. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP023544 (Campylobacter jejuni strain CFSAN032806 plasmid pCFSAN032806, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

21. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017854 (Campylobacter jejuni strain ZP3204 plasmid pCJDM204L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

22. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to CP002030 (Campylobacter jejuni subsp. jejuni ICDCCJ07001 plasmid pTet, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

23. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP028186 (Campylobacter jejuni strain CFSAN054107 plasmid pGMI16-002, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

24. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP022471 (Campylobacter jejuni strain jejuni plasmid pRM1246_ERRC, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

25. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to CP013735 (Campylobacter coli strain OR12 plasmid pOR12TET, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

26. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017418 (Campylobacter jejuni strain MTVDSCj13 plasmid pMTVDSCj13-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

27. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017419 (Campylobacter jejuni strain MTVDSCj16 plasmid pMTVDSCj16-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

28. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017866 (Campylobacter coli strain YF2105 plasmid pCCDM105L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

29. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017879 (Campylobacter coli strain BG2108 plasmid pCCDM108L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

30. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017416 (Campylobacter jejuni strain MTVDSCj07 plasmid pMTVDSCj07-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

31. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017872 (Campylobacter coli strain BP3183 plasmid pCCDM183, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

32. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP020775 (Campylobacter jejuni strain YH002 plasmid pCJP002, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

33. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NC_022355 (Campylobacter coli CVM N29710 plasmid pN29710-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

34. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_KJ646012 (Campylobacter jejuni strain 11601MD plasmid p11601MD, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

35. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP045793 (Campylobacter coli strain CFSAN032805 plasmid p1CFSAN032805, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

36. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NC_017282 (Campylobacter jejuni subsp. jejuni S3 plasmid pTet, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

37. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to CP047483 (Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

38. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to CP047483 (Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

39. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP013035 (Campylobacter coli strain HC2-48 plasmid pccdm1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

40. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP007752 (Campylobacter jejuni subsp. jejuni D42a plasmid pTet-D42a, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

41. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP014745 (Campylobacter jejuni strain OD267 plasmid pCJDM67 L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

42. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP023546 (Campylobacter coli strain CFSAN032805 plasmid pCFSAN032805_1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

43. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017026 (Campylobacter coli plasmid pCC14983A-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

44. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP011017 (Campylobacter coli strain FB1 plasmid pFB1TET, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

45. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017030 (Campylobacter jejuni subsp. jejuni strain 14980A plasmid pCJ14980A, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

46. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP014743 (Campylobacter jejuni strain WP2202 plasmid pCJDM202, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

47. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017877 (Campylobacter coli strain ZV1224 plasmid pCCDM224L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

48. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP044168 (Campylobacter jejuni strain AR-0415 plasmid pAR-0415, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

49. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP040609 (Campylobacter sp. CFSAN093226 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

50. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP017861 (Campylobacter jejuni strain TS1218 plasmid pCJDM218, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

51. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP043764 (Campylobacter jejuni strain BfR-CA-14430 plasmid pBfR-CA-14430, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

52. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP007750 (Campylobacter jejuni subsp. jejuni M129 plasmid pTet-M129, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

53. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP048762 (Campylobacter jejuni strain ZS004 plasmid pCJFEX, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

54. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_CP044170 (Campylobacter jejuni strain AR-0413 plasmid pAR-0413-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

55. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_MK541987 (Campylobacter coli strain CVM N46788F plasmid pN46788F, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

56. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_MK541988 (Campylobacter coli strain CVM N61740F plasmid pN61740F, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

57. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NZ_MK541989 (Campylobacter coli strain CVM N61925F plasmid pN61925F, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

58. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NC_022354 (Campylobacter jejuni subsp. jejuni 00-2544 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

59. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_KX686749 (Campylobacter coli strain Tx40 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

60. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP028373 (Campylobacter jejuni subsp. jejuni strain huA17 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

61. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP022078 (Campylobacter jejuni strain FDAARGOS_265 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

62. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP007182 (Campylobacter coli RM4661 plasmid pRM4661_48kbp, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

63. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017230 (Campylobacter jejuni strain FORC_046 isolate Not reported plasmid pFORC46.1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

64. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NC_006134 (Campylobacter coli plasmid pCC31, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

65. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NC_006135 (Campylobacter jejuni subsp. jejuni 81-176 plasmid pTet, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

66. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP007180 (Campylobacter coli RM5611 plasmid pRM5611_48kb, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

67. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017869 (Campylobacter coli strain MG1116 plasmid pCCDM116L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

68. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP044166 (Campylobacter coli strain AR-0416 plasmid pAR-0416) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

69. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP045046 (Campylobacter jejuni subsp. jejuni strain NADC 20827 plasmid p20827L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

70. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP010073 (Campylobacter jejuni subsp. jejuni strain 01-1512 plasmid pCj1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

71. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017857 (Campylobacter jejuni strain YQ2210 plasmid pCJDM210L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

72. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP023544 (Campylobacter jejuni strain CFSAN032806 plasmid pCFSAN032806, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

73. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017854 (Campylobacter jejuni strain ZP3204 plasmid pCJDM204L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

74. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to CP002030 (Campylobacter jejuni subsp. jejuni ICDCCJ07001 plasmid pTet, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

75. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP028186 (Campylobacter jejuni strain CFSAN054107 plasmid pGMI16-002, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

76. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP022471 (Campylobacter jejuni strain jejuni plasmid pRM1246_ERRC, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

77. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to CP013735 (Campylobacter coli strain OR12 plasmid pOR12TET, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

78. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017418 (Campylobacter jejuni strain MTVDSCj13 plasmid pMTVDSCj13-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

79. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017419 (Campylobacter jejuni strain MTVDSCj16 plasmid pMTVDSCj16-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

80. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017866 (Campylobacter coli strain YF2105 plasmid pCCDM105L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

81. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017879 (Campylobacter coli strain BG2108 plasmid pCCDM108L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

82. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017416 (Campylobacter jejuni strain MTVDSCj07 plasmid pMTVDSCj07-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

83. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017872 (Campylobacter coli strain BP3183 plasmid pCCDM183, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

84. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP020775 (Campylobacter jejuni strain YH002 plasmid pCJP002, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

85. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NC_022355 (Campylobacter coli CVM N29710 plasmid pN29710-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

86. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_KJ646012 (Campylobacter jejuni strain 11601MD plasmid p11601MD, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

87. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP045793 (Campylobacter coli strain CFSAN032805 plasmid p1CFSAN032805, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

88. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NC_017282 (Campylobacter jejuni subsp. jejuni S3 plasmid pTet, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

89. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to CP047483 (Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

90. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to CP047483 (Campylobacter jejuni strain CFSAN096297 plasmid CFSAN096297, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

91. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP013035 (Campylobacter coli strain HC2-48 plasmid pccdm1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

92. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP007752 (Campylobacter jejuni subsp. jejuni D42a plasmid pTet-D42a, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

93. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP014745 (Campylobacter jejuni strain OD267 plasmid pCJDM67 L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

94. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP023546 (Campylobacter coli strain CFSAN032805 plasmid pCFSAN032805_1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

95. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017026 (Campylobacter coli plasmid pCC14983A-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

96. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP011017 (Campylobacter coli strain FB1 plasmid pFB1TET, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

97. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017030 (Campylobacter jejuni subsp. jejuni strain 14980A plasmid pCJ14980A, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

98. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP014743 (Campylobacter jejuni strain WP2202 plasmid pCJDM202, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

99. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017877 (Campylobacter coli strain ZV1224 plasmid pCCDM224L, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

100. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP044168 (Campylobacter jejuni strain AR-0415 plasmid pAR-0415, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

101. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP040609 (Campylobacter sp. CFSAN093226 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

102. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP017861 (Campylobacter jejuni strain TS1218 plasmid pCJDM218, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

103. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP043764 (Campylobacter jejuni strain BfR-CA-14430 plasmid pBfR-CA-14430, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

104. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP007750 (Campylobacter jejuni subsp. jejuni M129 plasmid pTet-M129, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

105. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP048762 (Campylobacter jejuni strain ZS004 plasmid pCJFEX, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

106. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_CP044170 (Campylobacter jejuni strain AR-0413 plasmid pAR-0413-1, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

107. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_MK541987 (Campylobacter coli strain CVM N46788F plasmid pN46788F, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

108. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_MK541988 (Campylobacter coli strain CVM N61740F plasmid pN61740F, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

109. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NZ_MK541989 (Campylobacter coli strain CVM N61925F plasmid pN61925F, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctaatggaaaaagataaagacaaaaagggtgaaag	Protospacer
**   .*************.******.*******.

110. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NC_022354 (Campylobacter jejuni subsp. jejuni 00-2544 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.8

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
ctgattgaaaaagacaaagacaaaaaaggtgaaag	Protospacer
**    ********.****.**************.

111. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to NC_004996 (Streptococcus phage SM1, complete genome) position: , mismatch: 11, identity: 0.686

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
attcaggaaaaagaaaaaggcaaaaaatcccgtcg	Protospacer
 ****.******** ************  . .  .

112. spacer 5.1|1466783|35|NZ_CP018788|CRISPRCasFinder,CRT matches to AY007505 (Streptococcus mitis phage SM1,complete genome) position: , mismatch: 11, identity: 0.686

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
attcaggaaaaagaaaaaggcaaaaaatcccgtcg	Protospacer
 ****.******** ************  . .  .

113. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to NC_004996 (Streptococcus phage SM1, complete genome) position: , mismatch: 11, identity: 0.686

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
attcaggaaaaagaaaaaggcaaaaaatcccgtcg	Protospacer
 ****.******** ************  . .  .

114. spacer 5.6|1466784|35|NZ_CP018788|PILER-CR matches to AY007505 (Streptococcus mitis phage SM1,complete genome) position: , mismatch: 11, identity: 0.686

cttcaagaaaaagataaaggcaaaaaaggtgaaaa	CRISPR spacer
attcaggaaaaagaaaaaggcaaaaaatcccgtcg	Protospacer
 ****.******** ************  . .  .

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site
DBSCAN-SWA_1	96468 : 115927	22	Synechococcus_phage(43.75%)	NA	NA

Sequences of DBSCAN-SWA_1

Nucleotide sequences of DBSCAN-SWA_1

>NZ_CP018788|96468:115927|DBSCAN-SWA
AATGAGTCAAATTAAAGCAGTAATTTTTGATATGGATGGAGTATTGATAGAAGCCAAAGATTGGCACTATGAAGCGTTAAATAGAGCGCTTAGGCTATTTGGATTAGAGATTAGCTATTTAGAGCATTTAACCACATTTGATGGACTACCGACAAAGAAAAAGCTAGAGATATTATCAGTTGATAGAAAACTGCCTAAATCTTTACATAATTTTATTAATCAAATGAAGCAACTTTATACAATGGAGATTGTCTATCAATCTTGTAAGCCTAGATTTTATCACCAATATGCCCTATCTAAACTACATAAAGAGGGTTATAAAATGGCGGTTTGTTCTAATTCTATCTATAATACAATTGATGTAATGATGCAAAAAGCCGCCCTTAATCCATATTTGGATTTCTATATCTCAAATGAAGATGTCAAGCACGGCAAACCAGACCCAGAGATGTATAACAAAGCTATAGCCAAATTTGGGTTACAACCAAATGAATGTATGATAGTAGAAGATAATGAAAACGGCATTAAAGCAGCAAGAGCAAGTGGGGCTAATGTGATGATAGTAAAAGAAGTTAGCGATGTCAATTATGAAAATATCAAAGAGCATATTTTTAAATTTCAAAAGGGGGATTTATGATAAATATCGTTATTCCACTAGCGGGGAAAAGCAATTTTTTTAAAGAAGATGAGATTATCTTTCCTAAGCCTTTTGTTGAGATTTGTGGTAAAACCATGATAGAGATGTTGATAGATAATTATAAAGAGATTACCAACAAGCAATTTATTTTTATACTTAAAGATGATGATGTAAGCGAATTTCACCTAGATGAAGCTATCAAGGTATTAGACCCAAGCGCTCATATCATCACGCTTAAAAACCCTACACAAGGTATGGCGTGTAGCGCTCTTTTGGCTATTGATTATATAGATGATAACTCACCACTAATCATCGCTAATGCAGATCAAATTTTTGATATAAATTTAAATATTGTTTTAGATTATTTCAAAGATTATGATGCTGGGGTAATCGCCTTTGACTCTATCCATCCTAGATGGGCCTATGTAAGAGTGGATAATAGCTCAAATGTGATAGAAGCAGTGGAGAAAAAGCCAATTAGCAAAAATGCAATTGCGGGATTTTATTATTACAAACAAGGTGTGGATTTTATCCAAGCTAGTCAAAAAATGATAATCAACGACTCTCATTTAAATGGGCAATTCTATATAGCACCTACCTTAAATGAGCTTATTTTAATTGGTAAAAATGTTGGAGTATATAAGATAGATAATGAGTTATATCATACTTTTTATAGTATGGAAAAGATTAGAGATTATGAAAGGATTAAAAATGCTTAAAAGATTAACTCAAGATTATATAGATAGTTTTAACGCAAAAGATTTGGATGCTATATCAAGCATGTTAAGCGATGAGTTTTCATTAGAAGATCCAATCGTTAAAAGGTTAGAAGGCAAAGATAAATGCCTAAAAGCTATTTTAAATATTTTTAACAATTGCCAAAATGTAAATTTTAAAGCCAAAAATATCTACACAGATGACAAAACTAGCTTTATAGAGTTTATACTGATTTTAGATGATAAGCATTTAGAGGGTGTAGATATCATAGAGTGGAATGAAAATTACAAAATTTCAGCCCTTAGAGCATATCTGTATGAGGAGGTGGCAAATGGCTAAGGTAGCATTATGTATAAGTGGAGCTTTTAGGGGTGAAAATTTTATAGAAGATATCAGAAATTCAATTAACGGCATTGCTGAGCCATTGAATGCCGATGTGTTTATTGCTTCATGGGATAGTTATAAAGTTTGGATGGGATTATGTGGTGGCAGTCCAGGATGGCTTAGAATACTATATAGTCAAAATATTATAGAAGCAGCGCCAAAAGAAATTGTCGTAGTCAACGCCGAATTTAAAGATAAATGTCCAAACATTTATAATGCATTGAATAGAGAAATTGATAGACCAATAACATCTAAAATTTTAAATAAAATACAAAAATTGCCAAATGTAAAAGGTGTTTATTTATCTAATGAGAGAGAGTTTTTACAAAAATATCCTTGCAAGTTAGATGTTGCAACTAGTTTAAAAATGACATATAATTACACAAGAGTAGCAAAGTTGATACAAGATTATGAAGAAAAGCATAATTTTTATTATGATTATATTATACATATTAGACCAGATTTTAAATATACGCTAAATTTTAGCATTGATACTTTAAAAAAATTAAAAGATAATCAGCTATATATAGCAATGCACCATTCAAATTCAACATCCGATATGCAATTTTTTGGCAGAAGATATGCTGTTTTAGAATTTTTAAGTTTATTTGATAAAGCTAAAAAATATTCTCATTTGCCATACTTTCAAGCATTTAAAGATGGAGGTGTTTGTTGTTGTTATAAATTAGGTGGCAATGGAGCTTACGAGGGCGGCATAGACCATCGTGTGCTTTATGAATGTGTTGCTTTTTTAGGTATAGAACAGATAGATAGCAAGACTTTACTTCCGTATGTTCGTATCAAAAAAAATCCTATTATGCCGCCCTTAAATGAAGCGATAAAAAAAGATAAAGAGCATTGGAAAAGTATTAAACTCAATGATCCTAGTGATTTTTTCAAAGCTTTGACTTGCAAGAAAATATTAAAATCGCAAAATGCAGATGAGAGAGTAAGAAATCAGTTGAGTTATAAATTGGGTCAAGCAATTATTGAATTGCCTATATATACACTACTATTTGCTTTGCTAAAAATTAAAAGAGATCATAAAATAGATGAAGCGATTTATCGACAATCTATTCAGAAATATCCAAATCTCAAGCTCCCACCACTTGAGACCTATCCAGATTATAATGAAGCCATAAAGATTAAAAACCATCTAAGCTACAAACTTGGAGAGGCTTTGATAAAAGCAAATAACAAAGGCTTTATCACCGGTGGGGGGGGGTATTGGCTACTATTTGAGATTAGGCGCATAATAAAAGAGCATAAAAAGGCAAAAAATGAAAATCGATAATTTAGATAGTATGATTCGTGGTTGGTTTGTAGGTGATTTTGAACCAAATGTATTAAAATCAGATCAAGTAGAAGTAGGGGTAAAAAGCTACAAAAAAGGCGACTATGAAGAGAGGCATTATCACAAAATAGCCACCGAAATCACAGTGATAACCAAAGGCAAAGTTAAAATGAACGGCGTGATATATGGCGAAGGCGATATCATCACGATAGTCCCATTTGAAGATACGGATTTTGAGGCTTTAGAAGATTCTCAAAATGTAGTAGTCAAAATCCCAGCCGCTAAAAATGATAAATATCTAGGTAAATATGGAGACAACAATGAGTAAAATAAATATTTTGATACCAGCAGCAGGGGCTGGGAGTAGATTTGCCAAAGAAAGATATACCAAGCCAAAGCCTTTTATAGATGTGCTAGGTAAGCCGATGATTGTAAGAGTTTTAGAGAATTTAAAAGTTGATGATGCACACTATATAATCATTTTACAAAAATCCCATTTCGAACAAGAAAAAGAGCTATGTAATTTAATAGCCAAAGATTATAATGTTAGCTTTGTATGCGTAGAGACTCTGACAGAGGGCACTGCTTGTTCTGTTTTACACGCTAGAGAACTTATAAATAATGATACGCCTTTGATGATAGCAAATTCAGATCAAATCGTAGATATAGATATCCAAAAATATATTTATGACACACTTGACAGGGGCTTAGATGGCTCAATTCTATGTTTTAAAGATTTAGAAAAAAGCCCCAAATGGTCTTTTGTAAAAATGAACAATGAGCTAATTGTAGAAGTAAAAGAAAAAGAGGTTATATCTGATATTGCTACAGTTGGAATTTATCTATTTTCTAAAGGAAGTTTATTTGTAGATTCGGCTATAGATATGATTGCGAGAAACGATAGAGTTAATAATGAATTTTATACTGCTCCAGCCTATAATTATGCAATTAAAAACGGAGCAAAAATTGGCTGTTTTTTGATGAATTTTGATGATATGCACGGTATAGGAACTCCAGATGATTTACAAAAATATATAAAATTTATTAAAGGATAATTATGATCCAAAAAAGATTAGCTATACAATTTTTTGGGCATACAAGAACATATAAAAAGACTTATGAGAGCTTTTTTAAAAATATAGTTGAACCTAATTTAAAAGATGGTTGGCAAATTGATATATTTATACATACTTGGGATATGAGTAGCAGCAGTGATAGAAGTTGGCATAATGGACAGGATTTATTCGACATTAATCTATTAAGTCAAAATGATATAGATGATATAAAAAGAGTATATAAACCAAAAAAGTTATTAGTAGAACATCTACAAGAAGGTGCTCACGGGGGGGGCGAATCTAAAAAAAGAGGAAATAGACTAAGAGAATCCTATGAAAAAGAAAATAGTATAAAATATGATTATATTTTATATACTAGAATGGATATTTTGTTTGCATCGCCTCTTAATATACAAAGATATATAGACTTATACACAAAAGGTAGTATGAAAAATTTTCCATTACCACAAAAGCATTGCTTTGCAGCATTTAATCCATTTGTGAGAATGCCTGTTATTGATATAAGATATATAAATGAGGGTGATATAGTTTATTTTACTAATTATCCACATAATGATTTTGAGCCAGATAAGTGCTTAGAACTCTTTATAATAATGATCGATTATAAATTGTATAGAGATTTTTTCTTACAAAGAAGAGATTTTATTCTTGGATATAATAGCTCATTAGCGGCCAAATTAAAAATAGAACAAGATAAATTATCTAAAGCTATGATAGCAAACTCTAAAAGCATATGGGGATATATAAGAATGCCTTATGTATTAAGCTATATAAAAGATATGTATAAAAGGAACAAATAGCCTATAATGAAAAGATTAAAGCTAACCCAAGCTTAAAGCTCCCACCACTTGAATCATATCCAGATTACAATGAGGCTGTAAAGATAAAAGAGAATTTAAGCTACAAACTTGAGAGGCTTTGATAAAGGCGAGTAGAGATTGGTATAAAGGCGGATATATTAAATTTATATTTGATATAAAAAAGATAAAAAATAGATAAATAAAATAGGCGTATTTATGGTGTTTTTATTGATATTATGATATAATGAATAATGATCTTTTATATAAATCAAGGATTAAAATCAAAATAAATAATTAAAATTTATGTCAAAAGGAGTATAAATGAAAATAGGTATTTTAGGTGCTGGAATATCTGGTTTATCTGTGGCTAGATTGTTAAAAGATGATTTTGAAGTAGAAGTTTTAGAAAAAGAATCAGTCGTAGGTGGCATAGCTAGAACAAGAGATGTAAATGGTATGGCCTATCATGTAAATGGTGGCCATTGCTTTGATTCTAAATATGATGATGTTAAGAAATTTGTTTTTGATACAGTATTGCCAAAAGATAAATGGAATTATATTCCTAGAAAAGCAGAGGTGCTGTTTAGAGATAGATGGATTAGCTATCCAATCGAATTTTCTATCAATCAAATAGATAAAATAGATTCGAATTTAGCTTTTAAAATCACAAATGAAATGTTTAATGCTTCTTATGAAAGTGGGGCAAATTTGCAAGAATGGTTTATAAACCACTTTGGAGAGACATTATCTAAAGAGTATTTTATACCATACAATACAAAAATATGGCAAATTTCACCTAAAGAGATGGATAGTGTTTGGATAGAAGATGAAAAACAAATGAAGCTCCCAGTACCAACTAAAAGAGGATTTTATGATGCTATATTAAATAGGCCAAATGATACTATGGTTCATAAAAATTTCTATTATCCTAAAACAAATAATCAAAACACATTTATAGAAGCTTTAGGCGATGGCTTAAATATTCTCACAAATTATGAAGTTAAAAATATAACGAAAGAAAATAACCAGTGGATTGTAAATGGAGAGAAAAAATATGGTATTTTGATTAACACAACACCACTTGATTTAATCCCAAATTTACTATCTAATATTCCAAGTGAAGCCTTGAGCGCATTTAAAAAACTTAAATTTAATAGAGTTACAAACATACTTTGGGAAACAGATGGTAGTTTAAATTTCACATGGGGATATATTCCAGATCCGAAAATAGGTTTCCATAGAATTAGCAATACCGGCTCGATTGTTCAGCCAAATGGTAAATTTTGTACAACAGAAGTTATAGGCAATGTGCCATACGAAAAGCTAGTACAAGAAGGTAAGAAATTATCGTTTTTAAAAAATCCTATTGATTATAATGTTACAGAACACGCCTATGTGCATTTTGACTTAAATTACAGCTCGGCCAAAAAAAGTGCCATCGATTATCTTAATCAATTGGGACTAATCTCTCATGGGCGCTTTGGTGAATGGGAGTATTATAATATGGATGTTTGCATTAAAAGATCAATTGATCTTGCTAATAAATTAAAATCTATGCACTTGTAATTGATTTTTATTGTCTTCAAGCCAAAGTGTAGTTTTTAAAAATTATGAAACTATAACTTTGGCATTATAAAATAGATATTAAATAAATAATTTTATTAAATTTTAATAATGATCTTCTTATAATAACCAAGAACAATTATTAATATTAATTTATCAAATTCCAAAAGGCCACAAATGAGAAATTTGCTATTTTTGCTCTTTATATCTTTAATTTTCATATCTTGCTCTTCAAGCAAAGCGCCATATTCTCCGCCTATTATAGATGATAACTTCACTCGTAATTCTCTAAAAACTCCTATATTAAATAAATTTGATTTAACAAACCCAAATAACCCCACCAACCAAACAAATATAACCCCATCAAATAATCAGCCAAATTCAGCTAATCAACTACCCCAAATAACCCAGCCACCGCTATTAACCGCCCCAGCTGCTCTAGGCTCATCCCCATCTCTTGGATCTAAATCAGCACCACTAACTATAATAAACCCAAAGGGTGGCTCAGCAATAACCGTTTGGGCATTAGTTCCTGGTAATTGGCTATGGGGATATACCTTAGATAACTCTAAAGAGTTTGGTAGAGCTAGGTCTTGGCAAGTTTTAAATCTAGGTAATGATATAGCTTTGATTATAAATTTCCTTACTAATACTTGTATCCATGATGAAGGTGGTGGTATAACTCACAGAGATTGTGATATCAATAACAAATCCCAACAATGGCAACTATCAGCTATGGATAATGGCGCCATTCAGATAAAATCTAGTGCTTCTAGTAAGTGTATCACAACAGATCTTGGCTCACTAACTCAAACTGGTAGCTACTACAGTCTTGCTATGAGAGAGTGTAATTTTAAGCCAAATTTCAATCAACAATGGGTATTTATCCCTGAAGCAGCACCAACCTCACCACTCTTAGGATACCAACAATGAAAAATCTATTAATAATACTATTATTTAGCTTTATAAGCTTATATGCTAATATAGATGATTTTAAAACAGCCACTTGGAATATGCAAGGCTCAAGTGCTAGTAGCGAGGCTAAATGGAGCATTAGTATAGCTCAAATGTTCTCAGGAGCAAATGGAATAGATGTCTTAGCCATCCAAGAAGCTGGCACCTTACCTGCTACAGCCGAGCCAACTGGAAGGGAGTTTAGAGCATTTGGTACTAGTGTGGTTGTAACTGAACATGTGTGGAATATAGGCACAAGATTAAGACCTGATCTAATCTTTATATATTATGCTAGGACAGATTTAGGTGGTAATAGAGTAAATTTAGCCCTAGCTAGTAGAAGACAAGCTGATGAAGTATTCTTACGACCACCTCCGACAACAGCCTCAAGACCAATGCTAGGAATTAGAATTAATAATGATGCATTCTTTAGTATTCACGCATTAGCTAATGGCGGAGCTGATGCTTCAGCTATAGTTCATAATATAGATCTATTCTTTCAAAGCAGCCCAACCCTAGCTAATACCAATTGGATTATAATGGGGGATTTTAATAGAGAACCTGTAGATCTACTTAGCTCATTTGAATTAGAGTTAAGACTTAGAACTAGGATAATTACTAATAACGCAATAACTCAAATAAGTGCTAGAAGAACTCTAGATTACGCTGTAGTAGGTAACTCCAATAGAGCTATCGCACCAGCACCACTACCACCAATATCAGCTAGCACATTCTTTAGTGGATTTAGAACTCACATAGCAAGTGATCACTTCCCTGTAACATTTAGGAGATTTCCATGAAAATAGCTATAAAAATATCTTTAATATCTTTAATCTCTATATTTATCATTGGTTGTAGCGGAGCTAAAGTAGAACAACCAAAGCAAGATATGAGCTTTTTAAAGCTTGATGACTCTAAGGGATTTGCAGGAGATATAAGCAAAGCCCCAGATGAAACAAAAGCCCCAGATAGAGATCCATTATTAAAAGATGAAAAAACACAAACACCAATCTTAACTAGCTCAAATAATCAAGATGGGTTTGATCCATTTACCTTGCCTTTAAGTCTAAGATCACTTGATACAGGTATGCCTTTAGTAGTCAATTTAAATAAATCAGATGAAACTTTTAATTATAACCTAAGAGAGATTAAGGCATTTGAGCCAACTATAATTAGTGAGATTAAAAGGGTTGATAGCTTTGCACATTTAAGCCTTGAGTATGTGCAGTTTGTATCAGCTAATGATATAAATAGTTGCCTCGGGATTGATGAGAGTGGATTTTTTGCTTTAAAGAATTGTATTGGGGATTTAGATAGAAAGAAGTTTGAAACTGTATTTCAACTCATCCCACTACTAAGTGATGCTGTAGAGATAAGATCACTAGTCCTAGGTGGTAAAGAGTGTATAAGTACATTTGAAAATCCAAATTTAGAGCCATGGCAAAGAGTAGGAATAAATAGATGTGAATTAAGAGAGGGCTTTAGCGTAGATGCATCTAAACTTTGGGCTATTATGCCTGAAATAAAAGAAGCAGCCATAATCCAACCGGTGGATTGAGTTAAAATAAGTAGATTAAATCAATCAAATTCCGATCAAAATATAAATAAATCTTATAAGAAATTTAGGTTTGGTGGATGAATTTAGGTTACTAAATAAAGTAAAAATTATTTATTAAATTTAAAATTTCAATTTTAAATTTAAAATTAATAAGATTGTGTTATAGAAGAAAATTAATTAATATCAATAAAAGCTTGATAGTCTTGCGGGATTCCAATATCAATAAAGTAGTCATCAAATACGCAGGCTCTAGCTTTGAGAGCTAAAAAATTATTTTGAAAAAACTCTTCAAATGAGAATTTGGCATTTAAACTAAAATCGTCAAATATATCTTTACTAACTAGATAAATTCCGCCATTGATAAATCCATCGGGTGTGAATTTTTTCTCATTAAATGCTGTTATATTATGATTTTTATCGATATTTACACTCCCATATCTATCAAAATTATTCATATGTTTTAAAGCTATACAAATTTTGCTATCATCTAGTTTTAAATTGTTTAGATTTATATCAAAAATTGTATCACCATTAAGTATATATACGCTATTTTGATCTACTAATTTTAAAGCTTCCATAATCGCTCCACCAGTGCCTAGTGGCTCATCTTCTATGCTATAGACAATCTCTATATCTAGATATGAATTTTGAAAATAATTTTGTATTATTTCATATTTATATGAAACGGCCAAGATAACTTTTTTGATATTTTGTCTTTTTAAATACTCTAGGATAAACGCTAAGAAAGGTTTGTTTTTAACAGGCGCCATAGGTTTTGGCAGGTTTGGTAACACGCTTTTAAGGCGTGTCCCAAGTCCGCCACATAATATGATCGCTTCTTTAGGGCTATTCATCTATTTAAAACCTTTTCCAAATATCTCTTCTTCTACGATAGCACAAATAATATGCCCTATAACAATGTGAGATTCTTGAATTCTAGGGGTGCAATTTGATGGCACTTTGATACAATAATCACACAAATCAGCCATTTTGCCGCCGCTTTGACCAGTAAGCCCTATAGAGATTATCTCTTTTTCTTTACATACTTTTAGGGCTTCTATGATATTGGTGCTATTTCCGCTTGTTGATATTCCTATAAAAATATCACCTTTTACGCCTTGGGCTTGAACTTGTCTAGCAAATAATCTATCATACCCATAGTCATTACCAATAGCTGTTAAAATGCTTGTATCAGTAGTGAGGGCTATGCTAGGAATTCCGGGCCTATCAAAATAAAATCTACTTACAAACTCACCTGCTATATGTTGGGCATCGGCAGCACTCCCGCCATTGCCAGCGAGCATGGTTTTAAAGCCATTTTTGTAAGCATTTGTAGTGATTAAGGCCACCTTTTGGATAAGCTCTATTAGGGCTTTATCTTGTAAAATTTGATTTTTTACTTGTATTGAGTCTTCAAAATGACTTTTTATATATTGATTTATAATTTCCACGATTTTGCTCCTTCTTTGGTAAATGAGAAGTCTTGGACATATCCTGATTGTTGATTTAGAATTTTAATTAGATTATATTTTTTGATTGGATCTACTAAGAAAAACATAAATCCACCCGCTCCAGCTCCACTAGTTTTGCCGCTATATGCGCCATTTTCCATAGCTAGATTATAAATTCTGTCTAATTCATCGTTGCTAACTATATCGGAGATAATTTTTTTAGATTTCCAAGATTTGCCTAAAATTTGAGCTATAGTATCAAAATCAGCCCTAAATAGAGCCTCTTTCATAGCTACCGCATCTTGTTTTATCGCATGCATTGCCTCAAGTGATTTGCTATCTCCTAATTTGCCTTTTTTGTGCTCTTCTATATCTTTGGCTTCTCTAGTAATGTTGGTAAAATATAAAACTACTCTAGATTCAAGCTCGCTAGCGATCCAATTTTTGATTCTTAATGGATTTACAATTACTCTTTTATTGTCATAAAATTCCATAAAGTTAAATCCGCCAAAGGTAGCAGCGTATTGATCTTGAGCGCCACCTACGATTCCTAAGTCTTCACGCTCGATTTCATAAGCAAGTTTTGCTATATCATATTCTCCAAGTGGTAGATTTAGCCATTCTGTGAATGCTTGAATTATTCCTACGACTAGAGTAGAGCTCCCACCAAGGCCACTTCCACTAGGGACATCTGAATATGTATGGAGCGAAAAACTTAAAGGTTTATAGGTAAAATCTTTTACAATGCGATTATAAACTGCCTTAAAAATATCTAAATTTCCATCATTTTCTAAATGCAATTTGCTATTGTATTTTGCGTATGAGTTAGTATCTGGCGAATCAAATATAATTGTGTTATCATCTCTTGGGATTAATGTGCAATGAATATAAAGGGATATCGTAGTATTTAAAACATAACCAGTGTATTTATCACAATATAAATTGATATCTGTACCACCGCCAGCTAATCCTAATCTAAGCGGGGTTTGAGAACGAATAATTTTCATAAAATTTCCTAATATTTTAAAAAATGGAACGATTAATTATAACCTAAATAAATTAAAACTAGTATTAAACTATTATATTAATTTTCTATTGTTACAAAAGCAGTAAAAACCAACATAGCTTTTGGTTTGATTATAGTTTAAAATAGTCCAAATTTCTTTTATTGAGTGTTTTGATTCTAATAATTTTTTAATCTTATCAATATCTTTATCATAAAAGCTATTAAATGAATTCTTAATGAGATATATAATTTAGCAGCTCAAAGCCATGTACATGTGAGTTTCGAAACGCCAGAATACACAGCAAATGCCGATGCCTTAGGAACTTTGAGAATTTTAGAGGCGGTTAAATTCTTAGGCTTAGAATCAAAAACAAGAATATACCAAGCATCTACATCTGAATTATATGGAAAAGTTCAAGAGATACCGCAAAATGAAAAGACTCCATTTTATCCACACAGTCCTTATGCCGTGGCTAAAATGTATGCTTATTGGATTACTATAAATTATAGGGAGGCTTATAATATTTTTGCTTGTAATGGAATTTTGTTTAATCACGAAAGTCCGATTCGTGGCGAGACATTTGTAACTAGAAAAATTACTAGAGCTGTTTCTAAAATAGCTTTAAATTTACAAGATTGTGTATATTTAGGAAATCTAAACGCAAAAAGAGATTGGGGACATGCTAAAGATTATGTAAAAATGATGTGGCTTATACTCCAATATAAAGAGCCAAAAGATTGGGTGATTGCTACTGGACAAACGACAATGGTTAGGGATTTTGTGAAATTAGCTTTTTTGTATTGCGGGATAGAGCTTGAATTTAAGGGTCAAGGCGTTGATGAAATAGGCGTGATATCAAGTATAGATTATCAAAAGGCTTTGAATTTAAATATCGATCTATCTCATCTTAAAATAGGCCAAGTAGTGGTGAAAATAGATCCTAGATATTTTAGACCTACAGAGGTTGATCTATTGTTAGGAGACCCAAGCCAAGCTCAAAATGAATTAGGTTGAAAAAGAGAATTTTCTTTATCTGATTTGGTAGATGATATGATGCAAAGCGATCTAAATTTGATGAAAAAAGATCAATTTTTACAAAATAATGGTTTTAAAATTATGCGTTATTATGAGTAATAAATTTAGATAAATAGCAATATTGCTATTTATCTTTAAGTATATAAATTTATCTATTTAGAGGGATTCTACCTTTTTTGATCTCATCTCTCCAATGATTTAACAGGTCTTCAAACATCTTTCTAGCTGGAATCTCTGGCTTCCAATTGATAAAGCTTTTGATTTTGGTATTGTCAAACATTTGATAATCAGCATCAATTGGGCGAAGTCTATTAGCATCTTCTTGAATTTTGATATCATCTCTTTTTGAAAATCCAAGCAATATATCTATAACTTCAGGTAGCTTAAATGCCTCTTCTCCTGCTATATTAAAAGCCTCTCCGCAAGGGACTTTGCCTTTTTGGCTCTCTAGCGATAAAAGATAATACGCTCTAATAGCATCACGGCAATCTTGGAAAGTTCTAACACTTGATAGATTTCCAACTTTTATAATTGGCTCTTGCAGGCCTGCTTCTATTAGGGCAATTTGCTTAGCTACTGTACTTTCAAAAAAGACATCGCTACGCCTTGGGCCACTATGTGTTCCCATTCTAGTTACATAGGTTTTAATACCATAAGCCTCGCCATAAAATCTACCTAAATAGTCAGTTCCGATTTTGCTAATGCTATATGGACTAGCGCCGTGAAATGGGGTATCTTCATTTAATTTTATTCCAACTTTTGCTCTACCATAAACCTCGCTTGATGAGCATACATGGACAACTGGGTCATAACCATCTTTTTGTTTTAAGGCTCTTATATTTTCTAATATATTTGCTGTGCCTATGATGTTTGTTTGTAGTGTTTCGATTGGAATATCAAAAGAAGTTTTAGGAAAAGACTGTGCAGCTAGGTGAAAAATAACATCCGGACGATGAAATTCAAAAAGCTTTTGAATACTTGAATAGTCATTTAAATCAGCGTAATATACGCTTATTCTATCATTTTTATTGATTCTATCGCTTAAATGATAGATATTATCCATAGGTTCTTGCCAACGCATCATACCTATAATTTCATAATCTGTATTTTCTAGTAGAAAATCAGCCATTTGAGAGCCTACTTGCCCTGTAAATCCTGTAATTAGAGCTTTCATTATTAAATTTCCTTAAAATTGAATTACATTATGGTAGCATTTAATTGCTAAAAATATTATAAATTATCTACTCCAAACACCATACATTTCTATCATTTTTTTAAGACCATTTTTTAGCGAAATTTTATTTTGGTATCCGAGTTTATTAATTTTTTTCCTACTCATTGTTTTTCTTAATGTTCCATCATTGCGACTTAGTTCTTTTTCAAAAATTAACTCACCTTTATAATCCATCAACTTAACAATTAAAAACGATAGCTCTTTTATACTTACTGGCTCTCCATCTGTAAAATTTACAAATGAACTTATAAGATTACCATTTTCATCATATTCGCAAAGATCTTTGAAGTCTATATTTTGTGCTAAATATATACAAAATCCAGCTAAATCTCTAGAATTGGCAAATTCTCTAGCTGCAGCACCAGTACCAATCATCTTGATATAATTGTCAAATATACCATGCTTATCGCAAAATTCCAAAGCCTCTTTTTGATTTAAATTTAAATCCTTACAAAGAGCATTTATATTATTTTCATTACGCATTTTAGCTAGATATATCTTTCTAAAAATACCGGCTTGTACATGCGAATCTTCAATATTAAAATTATCATTTTCTCCATAAATACTAGTTGGTGCTACACATAAAAAGTTTTTTCCTTTTTCTAAATTTAGATATTCACATAGTTTAATTCCTGCTACTTTGCCTATAGCATAGCTTTCATTATTAGGTTGAAAAGCACCTTCGAGCATATATCTTTCTTCTAATGGCAATGGCGCATCCTTAGGAAAAACACATGCAGAAGCTAGATAAATTAACTTTTTAACTCCATTATTTGCAGCAGCCCAAATAACATTATTTTGCATCATGATATTATTGTATAAAAATTCAGCCGGATATTTCTTTTGTTTGATAAATCCACCCGCAAAAGCAGCACTGAAAAATACATAATCAGGTTTTTCTTGTTCAAAAATTCATTTACAGCTTTTTGATTAATCAAATCCAGTTCATTATGGGTTTTATATATTAAATTTGCATATCCTTGCTTTTGCAATTCCTCTATAATTGCACTACCTACTAAGCCTCTATGCCCGGAGATATAAATTTTAGAATTTTTATCCATTGCAAATCCTTTTAGAATCTGCAATGAAATTTAAGTTATTTATTGCATTAAATGTAGTTGTATAGGTTAAATTTATAAATTTAGACTCTACCCCCTCCCCTTAATGCTAGTTTTATACCATTGATACATCATTTTAATACCTTCTTCTAACTCGATTTTATGTTTCCATCCTAGTGAATTTATCTTAGAAACATCCATTAATCTATCCATTGTTGAATCTGGTCTAGATGTATTAAAATATAACTGACCATTAAATCCAACAATGCCTTTAATCATATCAACTACTTCTGCAATACTATAAGCAACTCCAGAGCCAATATTAATATGAGTATTTTGAGGATTTTTGCCCTTAGCTAAATCGCTAAAATTAATATTTTCCATAGTAAAAATACTAGCATCGGCTAAGTCATCACTATGGATAAATTCTCTTTTAACCTTACCGGTCCCCCAAATTTCTACACTATCTTTAGCGATTCCATAATTATTTAGAATTTCAGTTGCTTCTTTTTCATTCATATTTAAATCTGCCAAAACACCTTCAAAATTATCATCTTCAAGCATTTTAGCTAAATGAAATTTACAAAGCAAAGCAGGCAAAACTCTACTTTTGCCAAAGTCAAAATTCGCCCTTGTGCCATATAGATTATTTAATGCCAAGCATAAGAAATTTGTGCCATATTGTATATTATATGCCTCACACATTGCAGCCCCAGCTATCTTAGCTATACCCATAGTATATGCGTTATACTCTAAAACGCTTTGCATCATATACTCTTCTTTTAATGGATTTTTGGCATGATATGGATACATATAGCCAGAGCCATAGCATATAAGCTTTTTAACACCATGTAAATAAGATTGATGAATGATATTATTTTGTATCATCAAATTTACATAGATAAAATCAGCTCTTTGCGCTACATTTGCAGCACCGCATGGTAATACGGCACATAAAAACACATATTCAGGTTTTTCATTTTTAAATAAATCTGCAACTGCCTCTTGATTAGTCAAATCAAGCTCTTGACGAGTTCTAAGTATTAAATTATTATAGCCTCTAGCCCTTAAATTATCCACAAGCGCCGTCCCAGCCGTCCCATTATGCCCAGCTATATAAATTTTAGAGTTTTTATCCATTTAAAATCCTTTAGTGTGATCTTGAGTCATTGCTTCAATATCTCTATTTGATAAAATTGGAGTATTAGTAGGCCAATCAATTGCGATTCTAGGATCATTCCAAGCAAATGTAAATTGATCACTTGCATCGACATATTCACCCTCATAAGCCCATTTGTAATAATACATAGAGTCGCATTTTGAGCTAACATATTGAGCATTGCCAAATCGTGGCGGGATTAAAATTAATTTTTGATTATCTGAGTTGATAATGAATTTTTCGTATTGTAGATATGTTGGAGATTCTTTTTGGCAATCTACTACAACTTGGTGAATTTCGCCAGTTACGCAAGTTACAAGCTTCCAAGATTTATGATCGCCATGAATGCCTCTTAAAACATTTGGTTTTGAAAGTGTAAATTTATCAAGGACAAAATTAAGGCCATTTGGTAAAAGTTTTAATATCGCTTCGCTTGAATACGCCGACCAAATCTCACCCCTTAAATCTTTGAATTTACTAGGAGTGATGATATAAACGCCTTTTAGTTTTTTAGATTCTTGTATGTCAAACTCTATCGCCATCACGCAGCCTTTAAACCTAAGCCAAAAGGCATAGTGAAATTGCAATTTGAATATAAATGAGTAAATTTAGAATTATTTATTGATTTTAAATTTAGCTCATACCCCCCCATTTTTATACCATTGATACAGCATTTTGACTCCTTCTTCTAAATTTATTTTATGTTTCCAGCCTAAAGAGTGAATTTTTGAACAATCAGTTAGTTTATTCATTGCTCCATTAGGGCGATTAGCGTTAAAGGTCAAATCGCCTTTAAATCCAACTATCTCTTTGATTAATGTTGCTAGCTCTTTAATTGTAATATTTTCATTTGGGCCTATATTTAGATGGGTATTTTGTATCTCTTGTGAGTTATCGATAAGATCTTTAAAGTTTATCTTTTTCATGATAAACAAGGCGGCCTCTGCTAGATCATCACTATGTAAAAATTCTCTTGTAGGAGTCCCATCGCCCCATATTTCTACGCTATTTTCATTTATACCAAATTTGTTTAAATAAACTAAAGCTTCATCTAAATTTGGCATATTTAAATCATTTAGTAGCTCATCATATCTATTTTCATTTAGGAGTTTGGCTAAGTGCATTTTTCTTAAAATTCCAGGGACTACATGTGATTTTTCTAAATCAAATTTATCATTATTCCCATATAAATTTGTAGGGGTTATGGATATAAAATTTGTGTTGTATTGTAAATTATAGGACTCACACATCAAACAACCAGCGATTTTGGATAAGGCATAAGGCTTATTAGCATAATCCAAATCACCTTTTAACATCCAAGATTCATTAGTTGGTAAGGTGGCGTTTTTAGGATAAACTGTAGTTGAAGCTATAAAAAGCAATTTTTTAACACCATTTAAATATGCTTGATGGATGACATTACACTCTATCATTAAATTTTGATAGATGAAATCTGCTCTATATTTGCTATTGGCGCCTATGCCACCAGCTTTGGCGGCACAGAGTATCACAAATTCCGGTTTTTCTATCTCAAAAAATTTTTTAACTTCTTGCTGATTAGTAAGATCTAATTCATCATGTGTTTTATATATCAAATTTAGATAACCATCATTTTGTAATTTTCGTAAAATAGCACTACCGACTAGACCTCTATGCCCTGCGATATAAATTTTAGAGTTTTTCTCCATTTATTTCCTTGATAATAGGCTTATTTAACCCATAATTATTACATTAATTCGCCTAATTTTTACTTAAATTTAAGTTTTAATTTTGTGTGATAAGCATATCTCGCTCTGATAAAATCGGATTAGTTGTAGGCCACTCTATGCCTATTCTAGGGTCATTCCAAGCATAAGTAAATTGCTCATCTGCGTCTGTATATTTACCTATATATGCACATTTGTAATAATATACCGCACTTTGCGAGCTAACATAATGAGCATTGCCAAAACCAGCTGGGACTAAAATCATCTTTTGATTATCAGCATCTATTACAAACTCTTCATATTGTAAATATGTAGGTGAGTTTTCGTTACAATCTACTACTACTTGGTGTATTTGTCCATATACGCAAGTAGCTAATTTGTATGTATTTTTATCGCCATGAATGCCACGGATTACATTGTGCTTTGAGTGAATAAATTTATCATGGATAAATCTTAGATTATTTGGAAGGAGTTTATCGATAGCTTCGCTAGTAAATGCTGACCAAATCTCACCCCTTAAATCCCTAAATTTATTAGGAGTGATGATATAAACGCCTTTTAGTTTTTTAGACTCTTGTATATCAAATTCTATCGCCATCACGCAACCTTTAGCTCGCTAAGATAAGCGATAGAAATTTGAAATTTATTATTTAGAGGTCTGCCCCCCCCCACTATAACGCTATTTAGCAAATTTATTTGATTACTAATATCTATTTGGTGATTGCCTACGAAAAATCCATTTTCTTGCAGATATTTTGCGTTTTTTAGTTCGCCAAAAATTTCGTAATCAAAATATTTGATAACCTCATTTTGAGTAAAATCACCAGTAGCAATAGGGCGATACTCTATATTATTAGCTTCTAAAAGTTTGATAATATCAGCTCTTTTTAATTTTGAAGTAGGTTTTATAATGAGTGAAAATCCAAACCACGAGCTAGAGCCAATCTCTTGTTGTATGATAAAATCAGGATGATTTGCGAAGTATTTTTGGAAAAGCTTGGCATTTTCTCTTCTATGTTTTAAGAAATTTGGAAGTTTTTTTAGCTGTTCTATACCAATTGCTCCGCTCATCTCAACAGGGCGGACATTGTATCCAGGCAATACAAATCTAAACGACTCACTAAACCAATCATCGCTTTTTGGTGCTACTAGATTCTCTTTTGGCAAATTCCTAGTCCAACCATGCGCCCTAAGACATAATAAAATGTGATAAAGATCTTCATCATCAGTAACGACAAAACCACCCTCCATAGTAGCCATATGGTGAGAGTAAAATGTAGAAAATGTCCCCATAATACCGAATGTTCCGGCTTGTTTGCCTTTATATTCGGCTCCCATTGACTCGCAATTATCTTCTAATAAAATTATATTTTTATCACAAATCATAGCTTTAATAGCATCAAAATCATTTGGATTTCCGAGTAAATTGACACACATTATCATCTTTGTTTTATTGCTTATAGCATTTTTTAACGCTTCTAAATCATAATTTAGTGTATGTAAATCTACATCAACAAATTTGAGTTTAAGGCCATATTGATGAAGTGGGTAATATGTAGTGCTCCAAGATACGGCTGGGACTATTACTTCATCGCCTCTTTTTAGTTTATTATTTTTGGTATAAAATAGCGCTGCAGTTGCGATTAAATTCGCTGTCGAGCCTGAGCTTGTCATAACGGCGTATTTTGATCCGACAAATTTAGCGAAATCTTTTTCAAATTCGGCTACTTTCTTGCCCATTGTAAAGATATCGCTTTTGATAACTTCATTAATGGCGTTTAACTCTTTTTCATCCCAAGTTGATGATGCCAAAGAATACCCTTGCAT

Protein sequences of DBSCAN-SWA_1

>NZ_CP018788|96468:115927|103867_104692_+|WP_086301940.1|DBSCAN-SWA
MKNLLIILLFSFISLYANIDDFKTATWNMQGSSASSEAKWSISIAQMFSGANGIDVLAIQEAGTLPATAEPTGREFRAFGTSVVVTEHVWNIGTRLRPDLIFIYYARTDLGGNRVNLALASRRQADEVFLRPPPTTASRPMLGIRINNDAFFSIHALANGGADASAIVHNIDLFFQSSPTLANTNWIIMGDFNREPVDLLSSFELELRLRTRIITNNAITQISARRTLDYAVVGNSNRAIAPAPLPPISASTFFSGFRTHIASDHFPVTFRRFP
>NZ_CP018788|96468:115927|113032_114082_-|WP_086301948.1|DBSCAN-SWA
MEKNSKIYIAGHRGLVGSAILRKLQNDGYLNLIYKTHDELDLTNQQEVKKFFEIEKPEFVILCAAKAGGIGANSKYRADFIYQNLMIECNVIHQAYLNGVKKLLFIASTTVYPKNATLPTNESWMLKGDLDYANKPYALSKIAGCLMCESYNLQYNTNFISITPTNLYGNNDKFDLEKSHVVPGILRKMHLAKLLNENRYDELLNDLNMPNLDEALVYLNKFGINENSVEIWGDGTPTREFLHSDDLAEAALFIMKKINFKDLIDNSQEIQNTHLNIGPNENITIKELATLIKEIVGFKGDLTFNANRPNGAMNKLTDCSKIHSLGWKHKINLEEGVKMLYQWYKNGGV
>NZ_CP018788|96468:115927|103115_103871_+|WP_086301939.1|DBSCAN-SWA
MRNLLFLLFISLIFISCSSSKAPYSPPIIDDNFTRNSLKTPILNKFDLTNPNNPTNQTNITPSNNQPNSANQLPQITQPPLLTAPAALGSSPSLGSKSAPLTIINPKGGSAITVWALVPGNWLWGYTLDNSKEFGRARSWQVLNLGNDIALIINFLTNTCIHDEGGGITHRDCDINNKSQQWQLSAMDNGAIQIKSSASSKCITTDLGSLTQTGSYYSLAMRECNFKPNFNQQWVFIPEAAPTSPLLGYQQ
>NZ_CP018788|96468:115927|114697_115927_-|WP_086301949.1|DBSCAN-SWA
MQGYSLASSTWDEKELNAINEVIKSDIFTMGKKVAEFEKDFAKFVGSKYAVMTSSGSTANLIATAALFYTKNNKLKRGDEVIVPAVSWSTTYYPLHQYGLKLKFVDVDLHTLNYDLEALKNAISNKTKMIMCVNLLGNPNDFDAIKAMICDKNIILLEDNCESMGAEYKGKQAGTFGIMGTFSTFYSHHMATMEGGFVVTDDEDLYHILLCLRAHGWTRNLPKENLVAPKSDDWFSESFRFVLPGYNVRPVEMSGAIGIEQLKKLPNFLKHRRENAKLFQKYFANHPDFIIQQEIGSSSWFGFSLIIKPTSKLKRADIIKLLEANNIEYRPIATGDFTQNEVIKYFDYEIFGELKNAKYLQENGFFVGNHQIDISNQINLLNSVIVGGGRPLNNKFQISIAYLSELKVA
>NZ_CP018788|96468:115927|111325_112375_-|WP_086301947.1|DBSCAN-SWA
MDKNSKIYIAGHNGTAGTALVDNLRARGYNNLILRTRQELDLTNQEAVADLFKNEKPEYVFLCAVLPCGAANVAQRADFIYVNLMIQNNIIHQSYLHGVKKLICYGSGYMYPYHAKNPLKEEYMMQSVLEYNAYTMGIAKIAGAAMCEAYNIQYGTNFLCLALNNLYGTRANFDFGKSRVLPALLCKFHLAKMLEDDNFEGVLADLNMNEKEATEILNNYGIAKDSVEIWGTGKVKREFIHSDDLADASIFTMENINFSDLAKGKNPQNTHINIGSGVAYSIAEVVDMIKGIVGFNGQLYFNTSRPDSTMDRLMDVSKINSLGWKHKIELEEGIKMMYQWYKTSIKGRG
>NZ_CP018788|96468:115927|99828_100554_+|WP_086303179.1|DBSCAN-SWA
MNILIPAAGAGSRFAKERYTKPKPFIDVLGKPMIVRVLENLKVDDAHYIIILQKSHFEQEKELCNLIAKDYNVSFVCVETLTEGTACSVLHARELINNDTPLMIANSDQIVDIDIQKYIYDTLDRGLDGSILCFKDLEKSPKWSFVKMNNELIVEVKEKEVISDIATVGIYLFSKGSLFVDSAIDMIARNDRVNNEFYTAPAYNYAIKNGAKIGCFLMNFDDMHGIGTPDDLQKYIKFIKG
>NZ_CP018788|96468:115927|106888_107908_-|WP_086301943.1|DBSCAN-SWA
MKIIRSQTPLRLGLAGGGTDINLYCDKYTGYVLNTTISLYIHCTLIPRDDNTIIFDSPDTNSYAKYNSKLHLENDGNLDIFKAVYNRIVKDFTYKPLSFSLHTYSDVPSGSGLGGSSTLVVGIIQAFTEWLNLPLGEYDIAKLAYEIEREDLGIVGGAQDQYAATFGGFNFMEFYDNKRVIVNPLRIKNWIASELESRVVLYFTNITREAKDIEEHKKGKLGDSKSLEAMHAIKQDAVAMKEALFRADFDTIAQILGKSWKSKKIISDIVSNDELDRIYNLAMENGAYSGKTSGAGAGGFMFFLVDPIKKYNLIKILNQQSGYVQDFSFTKEGAKSWKL
>NZ_CP018788|96468:115927|110980_111238_-|WP_086301946.1|DBSCAN-SWA
MDKNSKIYISGHRGLVGSAIIEELQKQGYANLIYKTHNELDLINQKAVNEFLNKKNLIMYFSVLLLRVDLSNKRNIRLNFYTIIS
>NZ_CP018788|96468:115927|98152_99499_+|WP_086301935.1|DBSCAN-SWA
MAKVALCISGAFRGENFIEDIRNSINGIAEPLNADVFIASWDSYKVWMGLCGGSPGWLRILYSQNIIEAAPKEIVVVNAEFKDKCPNIYNALNREIDRPITSKILNKIQKLPNVKGVYLSNEREFLQKYPCKLDVATSLKMTYNYTRVAKLIQDYEEKHNFYYDYIIHIRPDFKYTLNFSIDTLKKLKDNQLYIAMHHSNSTSDMQFFGRRYAVLEFLSLFDKAKKYSHLPYFQAFKDGGVCCCYKLGGNGAYEGGIDHRVLYECVAFLGIEQIDSKTLLPYVRIKKNPIMPPLNEAIKKDKEHWKSIKLNDPSDFFKALTCKKILKSQNADERVRNQLSYKLGQAIIELPIYTLLFALLKIKRDHKIDEAIYRQSIQKYPNLKLPPLETYPDYNEAIKIKNHLSYKLGEALIKANNKGFITGGGGYWLLFEIRRIIKEHKKAKNENR
>NZ_CP018788|96468:115927|96468_97104_+|WP_086226139.1|DBSCAN-SWA
MSQIKAVIFDMDGVLIEAKDWHYEALNRALRLFGLEISYLEHLTTFDGLPTKKKLEILSVDRKLPKSLHNFINQMKQLYTMEIVYQSCKPRFYHQYALSKLHKEGYKMAVCSNSIYNTIDVMMQKAALNPYLDFYISNEDVKHGKPDPEMYNKAIAKFGLQPNECMIVEDNENGIKAARASGANVMIVKEVSDVNYENIKEHIFKFQKGDL
>NZ_CP018788|96468:115927|99485_99827_+|WP_086301936.1|DBSCAN-SWA
MKIDNLDSMIRGWFVGDFEPNVLKSDQVEVGVKSYKKGDYEERHYHKIATEITVITKGKVKMNGVIYGEGDIITIVPFEDTDFEALEDSQNVVVKIPAAKNDKYLGKYGDNNE
>NZ_CP018788|96468:115927|105623_106304_-|WP_086301942.1|DBSCAN-SWA
MNSPKEAIILCGGLGTRLKSVLPNLPKPMAPVKNKPFLAFILEYLKRQNIKKVILAVSYKYEIIQNYFQNSYLDIEIVYSIEDEPLGTGGAIMEALKLVDQNSVYILNGDTIFDINLNNLKLDDSKICIALKHMNNFDRYGSVNIDKNHNITAFNEKKFTPDGFINGGIYLVSKDIFDDFSLNAKFSFEEFFQNNFLALKARACVFDDYFIDIGIPQDYQAFIDIN
>NZ_CP018788|96468:115927|112375_112936_-|WP_086251207.1|DBSCAN-SWA
MAIEFDIQESKKLKGVYIITPSKFKDLRGEIWSAYSSEAILKLLPNGLNFVLDKFTLSKPNVLRGIHGDHKSWKLVTCVTGEIHQVVVDCQKESPTYLQYEKFIINSDNQKLILIPPRFGNAQYVSSKCDSMYYYKWAYEGEYVDASDQFTFAWNDPRIAIDWPTNTPILSNRDIEAMTQDHTKGF
>NZ_CP018788|96468:115927|101696_102941_+|WP_086301938.1|DBSCAN-SWA
MKIGILGAGISGLSVARLLKDDFEVEVLEKESVVGGIARTRDVNGMAYHVNGGHCFDSKYDDVKKFVFDTVLPKDKWNYIPRKAEVLFRDRWISYPIEFSINQIDKIDSNLAFKITNEMFNASYESGANLQEWFINHFGETLSKEYFIPYNTKIWQISPKEMDSVWIEDEKQMKLPVPTKRGFYDAILNRPNDTMVHKNFYYPKTNNQNTFIEALGDGLNILTNYEVKNITKENNQWIVNGEKKYGILINTTPLDLIPNLLSNIPSEALSAFKKLKFNRVTNILWETDGSLNFTWGYIPDPKIGFHRISNTGSIVQPNGKFCTTEVIGNVPYEKLVQEGKKLSFLKNPIDYNVTEHAYVHFDLNYSSAKKSAIDYLNQLGLISHGRFGEWEYYNMDVCIKRSIDLANKLKSMHL
>NZ_CP018788|96468:115927|114158_114698_-|WP_086239276.1|DBSCAN-SWA
MAIEFDIQESKKLKGVYIITPNKFRDLRGEIWSAFTSEAIDKLLPNNLRFIHDKFIHSKHNVIRGIHGDKNTYKLATCVYGQIHQVVVDCNENSPTYLQYEEFVIDADNQKMILVPAGFGNAHYVSSQSAVYYYKCAYIGKYTDADEQFTYAWNDPRIGIEWPTTNPILSERDMLITQN
>NZ_CP018788|96468:115927|104688_105450_+|WP_086301941.1|DBSCAN-SWA
MKIAIKISLISLISIFIIGCSGAKVEQPKQDMSFLKLDDSKGFAGDISKAPDETKAPDRDPLLKDEKTQTPILTSSNNQDGFDPFTLPLSLRSLDTGMPLVVNLNKSDETFNYNLREIKAFEPTIISEIKRVDSFAHLSLEYVQFVSANDINSCLGIDESGFFALKNCIGDLDRKKFETVFQLIPLLSDAVEIRSLVLGGKECISTFENPNLEPWQRVGINRCELREGFSVDASKLWAIMPEIKEAAIIQPVD
>NZ_CP018788|96468:115927|97815_98160_+|WP_086301934.1|DBSCAN-SWA
MLKRLTQDYIDSFNAKDLDAISSMLSDEFSLEDPIVKRLEGKDKCLKAILNIFNNCQNVNFKAKNIYTDDKTSFIEFILILDDKHLEGVDIIEWNENYKISALRAYLYEEVANG
>NZ_CP018788|96468:115927|97100_97823_+|WP_086268305.1|DBSCAN-SWA
MINIVIPLAGKSNFFKEDEIIFPKPFVEICGKTMIEMLIDNYKEITNKQFIFILKDDDVSEFHLDEAIKVLDPSAHIITLKNPTQGMACSALLAIDYIDDNSPLIIANADQIFDINLNIVLDYFKDYDAGVIAFDSIHPRWAYVRVDNSSNVIEAVEKKPISKNAIAGFYYYKQGVDFIQASQKMIINDSHLNGQFYIAPTLNELILIGKNVGVYKIDNELYHTFYSMEKIRDYERIKNA
>NZ_CP018788|96468:115927|110180_111089_-|WP_086301945.1|DBSCAN-SWA
MFEQEKPDYVFFSAAFAGGFIKQKKYPAEFLYNNIMMQNNVIWAAANNGVKKLIYLASACVFPKDAPLPLEERYMLEGAFQPNNESYAIGKVAGIKLCEYLNLEKGKNFLCVAPTSIYGENDNFNIEDSHVQAGIFRKIYLAKMRNENNINALCKDLNLNQKEALEFCDKHGIFDNYIKMIGTGAAAREFANSRDLAGFCIYLAQNIDFKDLCEYDENGNLISSFVNFTDGEPVSIKELSFLIVKLMDYKGELIFEKELSRNDGTLRKTMSRKKINKLGYQNKISLKNGLKKMIEMYGVWSR
>NZ_CP018788|96468:115927|100556_101375_+|WP_086301937.1|DBSCAN-SWA
MIQKRLAIQFFGHTRTYKKTYESFFKNIVEPNLKDGWQIDIFIHTWDMSSSSDRSWHNGQDLFDINLLSQNDIDDIKRVYKPKKLLVEHLQEGAHGGGESKKRGNRLRESYEKENSIKYDYILYTRMDILFASPLNIQRYIDLYTKGSMKNFPLPQKHCFAAFNPFVRMPVIDIRYINEGDIVYFTNYPHNDFEPDKCLELFIIMIDYKLYRDFFLQRRDFILGYNSSLAAKLKIEQDKLSKAMIANSKSIWGYIRMPYVLSYIKDMYKRNK
>NZ_CP018788|96468:115927|109091_110120_-|WP_086301944.1|DBSCAN-SWA
MMKALITGFTGQVGSQMADFLLENTDYEIIGMMRWQEPMDNIYHLSDRINKNDRISVYYADLNDYSSIQKLFEFHRPDVIFHLAAQSFPKTSFDIPIETLQTNIIGTANILENIRALKQKDGYDPVVHVCSSSEVYGRAKVGIKLNEDTPFHGASPYSISKIGTDYLGRFYGEAYGIKTYVTRMGTHSGPRRSDVFFESTVAKQIALIEAGLQEPIIKVGNLSSVRTFQDCRDAIRAYYLLSLESQKGKVPCGEAFNIAGEEAFKLPEVIDILLGFSKRDDIKIQEDANRLRPIDADYQMFDNTKIKSFINWKPEIPARKMFEDLLNHWRDEIKKGRIPLNR
>NZ_CP018788|96468:115927|106304_106901_-|WP_086226129.1|DBSCAN-SWA
MEIINQYIKSHFEDSIQVKNQILQDKALIELIQKVALITTNAYKNGFKTMLAGNGGSAADAQHIAGEFVSRFYFDRPGIPSIALTTDTSILTAIGNDYGYDRLFARQVQAQGVKGDIFIGISTSGNSTNIIEALKVCKEKEIISIGLTGQSGGKMADLCDYCIKVPSNCTPRIQESHIVIGHIICAIVEEEIFGKGFK

Homologous phage analysis in the prophage region

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_086226139.1|96468_97104_+	HAD family phosphatase	M1I080	Acanthocystis_turfacea_Chlorella_virus	3.2e-34	40.4
WP_086268305.1|97100_97823_+	glycosyltransferase family 2 protein	A0A1D8KNV9	Synechococcus_phage	7.8e-37	32.6
WP_086301934.1|97815_98160_+	nuclear transport factor 2 family protein	NA	NA	NA	NA
WP_086301935.1|98152_99499_+	hypothetical protein	NA	NA	NA	NA
WP_086301936.1|99485_99827_+	hypothetical protein	A0A222YXE6	Synechococcus_phage	1.8e-12	36.0
WP_086303179.1|99828_100554_+	glycosyltransferase family 2 protein	A0A1D8KNV9	Synechococcus_phage	6.2e-50	46.3
WP_086301937.1|100556_101375_+	hypothetical protein	E3T516	Cafeteria_roenbergensis_virus	2.5e-07	33.3
WP_086301938.1|101696_102941_+	NAD(P)-binding protein	NA	NA	NA	NA
WP_086301939.1|103115_103871_+	RICIN domain-containing protein	A5LH52	Enterobacteria_phage	4.6e-16	33.3
WP_086301940.1|103867_104692_+	cytolethal distending toxin subunit B family protein	A5LH53	Enterobacteria_phage	1.8e-61	48.5
WP_086301941.1|104688_105450_+	hypothetical protein	NA	NA	NA	NA
WP_086301942.1|105623_106304_-	nucleotidyltransferase family protein	A0A2K9L821	Tupanvirus	7.6e-10	31.5
WP_086226129.1|106304_106901_-	D-sedoheptulose 7-phosphate isomerase	A0A067XQR2	Caulobacter_phage	5.3e-15	31.1
WP_086301943.1|106888_107908_-	dehydrogenase	A0A222YW25	Synechococcus_phage	1.2e-54	38.1
WP_086301944.1|109091_110120_-	GDP-mannose 4,6-dehydratase	A0A222YY99	Synechococcus_phage	5.9e-147	72.5
WP_086301945.1|110180_111089_-	NAD-dependent epimerase/dehydratase family protein	M4R1H4	Synechococcus_phage	2.0e-45	34.8
WP_086301946.1|110980_111238_-	NAD-dependent epimerase/dehydratase family protein	M1HWW2	Paramecium_bursaria_Chlorella_virus	6.4e-10	54.9
WP_086301947.1|111325_112375_-	NAD-dependent epimerase/dehydratase family protein	M4R1H4	Synechococcus_phage	2.0e-65	41.7
WP_086251207.1|112375_112936_-	dTDP-4-dehydrorhamnose 3,5-epimerase family protein	NA	NA	NA	NA
WP_086301948.1|113032_114082_-	GDP-L-fucose synthase	A7IWS0	Paramecium_bursaria_Chlorella_virus	1.0e-82	45.7
WP_086239276.1|114158_114698_-	dTDP-4-dehydrorhamnose 3,5-epimerase family protein	NA	NA	NA	NA
WP_086301949.1|114697_115927_-	DegT/DnrJ/EryC1/StrS family aminotransferase	E5ES46	Bathycoccus_sp._RCC1105_virus	5.9e-45	33.7