CRISPRimmunity

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Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_CP024595	Porphyromonas gingivalis strain KCOM 3001 chromosome, complete genome	6 crisprs	cas3,cas13b,Csx28,Csx27,DEDDh,cas6,cas5,cas8b6,cas7,cas4,cas1,cas2,cmr1gr7,cas10,cmr3gr5,cmr4gr7,cmr5gr11,cmr6gr7	0	23	1	2

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP024595_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024595_1

264811-265375

TypeVI-B1,TypeVI-B2

VI-B2

Consensus_repeat	Method
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	PILER-CR
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	CRISPRCasFinder
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA	CRT

8 spacers

Csx28,cas13b

The CRISPR arrays of NZ_CP024595_1

>merge|NZ_CP024595|1|264811-265375|PILER-CR,CRISPRCasFinder,CRT
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACAGAATACTTGAGCCGGCGATCTTGAGTATCGTTGGATCTACCCTCTATTCGAAGGGTACACACAACACAGATTCGATTCGTGCCTATAGATTATCAGTTGGATCTACCCTCTATTCGAAGGGTACACACAACAGGTTATACCTGTCCTCGTCTTGTGCGTGCGTTGGATCTACCCTCTATTCGAAGGGTACACACAACATTTTCTTTAACTGTATCTAATATATTAGTGTTGGATCTACCCTCTATTCGAAGGGTACACACAACTGCAGACGCAGGCGGGTATGCCCGATCTTGGTTGGATCTACCCTCTATTCGAAGGGTACACACAACGGTGAAGTGTTTTATCTCGTTGTCGAAATAGTTGGATCTACCCTCTATTCGAAGGGTACACACAACAAGGGAATATCTCTCCCTTGGCAGGCGTTCGTTGGATCTACCCTCTATTCGAAGGGTACACACAACAAGTCGTACGCGAACACGTGCGGATTGCTCGTTGGATCTACCCTCTATTCGAAGGGTACACACAACA

>NZ_CP024595|1|1|264811-265374|PILER-CR
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AGAATACTTGAGCCGGCGATCTTGAGTATC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	ACAGATTCGATTCGTGCCTATAGATTATCA
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AGGTTATACCTGTCCTCGTCTTGTGCGTGC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	ATTTTCTTTAACTGTATCTAATATATTAGT
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	TGCAGACGCAGGCGGGTATGCCCGATCTTG
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	GGTGAAGTGTTTTATCTCGTTGTCGAAATA
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AAGGGAATATCTCTCCCTTGGCAGGCGTTC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AAGTCGTACGCGAACACGTGCGGATTGCTC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC

>NZ_CP024595|1|1|264811-265374|CRISPRCasFinder
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AGAATACTTGAGCCGGCGATCTTGAGTATC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	ACAGATTCGATTCGTGCCTATAGATTATCA
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AGGTTATACCTGTCCTCGTCTTGTGCGTGC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	ATTTTCTTTAACTGTATCTAATATATTAGT
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	TGCAGACGCAGGCGGGTATGCCCGATCTTG
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	GGTGAAGTGTTTTATCTCGTTGTCGAAATA
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AAGGGAATATCTCTCCCTTGGCAGGCGTTC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC	AAGTCGTACGCGAACACGTGCGGATTGCTC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAAC

>NZ_CP024595|1|1|264811-265375|CRT
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA	GAATACTTGAGCCGGCGATCTTGAGTATC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA	CAGATTCGATTCGTGCCTATAGATTATCA
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA	GGTTATACCTGTCCTCGTCTTGTGCGTGC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA	TTTTCTTTAACTGTATCTAATATATTAGT
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACT	GCAGACGCAGGCGGGTATGCCCGATCTTG
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACG	GTGAAGTGTTTTATCTCGTTGTCGAAATA
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA	AGGGAATATCTCTCCCTTGGCAGGCGTTC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA	AGTCGTACGCGAACACGTGCGGATTGCTC
GTTGGATCTACCCTCTATTCGAAGGGTACACACAACA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024595.1\|WP_099779069.1\|256818_257727_+\|DMT-family-transporter	unknown	unknown	gnl\|CDD\|273359
NZ_CP024595.1\|WP_021664582.1\|253420_253939_-\|DUF4496-domain-containing-protein	unknown	unknown	gnl\|CDD\|273496
NZ_CP024595.1\|WP_099779071.1\|258749_259652_-\|tRNA-(adenosine(37)-N6)-dimethylallyltransferase-MiaA	unknown	unknown	gnl\|CDD\|234626
NZ_CP024595.1\|WP_097637691.1\|254614_256591_+\|transcription-termination-factor-Rho	unknown	unknown	gnl\|CDD\|236490
NZ_CP024595.1\|WP_099779070.1\|257737_258697_-\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|133030
NZ_CP024595.1\|WP_099779077.1\|274612_276070_-\|internalin	unknown	unknown	gnl\|CDD\|380191
NZ_CP024595.1\|WP_004584814.1\|251449_252352_-\|glutamate-formimidoyltransferase	unknown	unknown	gnl\|CDD\|226169
NZ_CP024595.1\|WP_004584826.1\|266437_267637_-\|methionine-gamma-lyase	unknown	unknown	gnl\|CDD\|168478
NZ_CP024595.1\|WP_021676668.1\|252392_253388_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779074.1\|267799_269269_-\|metallophosphoesterase-family-protein	unknown	unknown	gnl\|CDD\|277318
NZ_CP024595.1\|WP_004584829.1\|269965_270571_+\|YihA-family-ribosome-biogenesis-GTP-binding-protein	unknown	unknown	gnl\|CDD\|234770
NZ_CP024595.1\|WP_099779075.1\|269271_269865_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779658.1\|276634_278077_+\|exo-alpha-sialidase	unknown	unknown	gnl\|CDD\|271234
NZ_CP024595.1\|WP_005873836.1\|270580_271609_+\|UDP-glucose-4-epimerase-GalE	unknown	unknown	gnl\|CDD\|187558
NZ_CP024595.1\|WP_005873802.1\|273747_274518_+\|HAD-IA-family-hydrolase	unknown	unknown	gnl\|CDD\|223710
NZ_CP024595.1\|WP_097637689.1\|264056_264602_+\|hypothetical-protein	Csx28	-	unknown
NZ_CP024595.1\|WP_099779076.1\|271651_273748_+\|ATP-dependent-DNA-helicase-RecG	unknown	unknown	gnl\|CDD\|236794
NZ_CP024595.1\|WP_021678157.1\|278141_278327_-\|DUF1661-domain-containing-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_077083535.1\|259667_260237_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779072.1\|260524_264052_+\|hypothetical-protein	cas13b	cas13b_CAS_V-B1	gnl\|CDD\|380475

Protein	Function_ID	Function_description	E-value
NZ_CP024595.1\|WP_099779069.1\|256818_257727_+\|DMT-family-transporter	gnl\|CDD\|273359	TIGR00950, Uncharacterized_inner_membrane_transporter_YicL, Carboxylate/Amino Acid/Amine Transporter. [Transport and binding proteins, Amino acids, peptides and amines].	2.36953e-12
NZ_CP024595.1\|WP_021664582.1\|253420_253939_-\|DUF4496-domain-containing-protein	gnl\|CDD\|273496	TIGR01201, HU_rel, DNA-binding protein, histone-like, putative. This model describes a set of proteins related to but longer than DNA-binding protein HU. Its distinctive domain architecture compared to HU and related histone-like DNA-binding proteins justifies the designation as superfamily. Members include, so far, one from Bacteroides fragilis, a gut bacterium, and ten from Porphyromonas gingivalis, an oral anaerobe. [DNA metabolism, Chromosome-associated proteins].	1.16618e-52
NZ_CP024595.1\|WP_099779071.1\|258749_259652_-\|tRNA-(adenosine(37)-N6)-dimethylallyltransferase-MiaA	gnl\|CDD\|234626	PRK00091, miaA, tRNA delta(2)-isopentenylpyrophosphate transferase; Reviewed.	1.65928e-126
NZ_CP024595.1\|WP_097637691.1\|254614_256591_+\|transcription-termination-factor-Rho	gnl\|CDD\|236490	PRK09376, rho, transcription termination factor Rho; Provisional.	0
NZ_CP024595.1\|WP_099779070.1\|257737_258697_-\|glycosyltransferase-family-2-protein	gnl\|CDD\|133030	cd04187, DPM1_like_bac, Bacterial DPM1_like enzymes are related to eukaryotic DPM1. A family of bacterial enzymes related to eukaryotic DPM1; Although the mechanism of eukaryotic enzyme is well studied, the mechanism of the bacterial enzymes is not well understood. The eukaryotic DPM1 is the catalytic subunit of eukaryotic Dolichol-phosphate mannose (DPM) synthase. DPM synthase is required for synthesis of the glycosylphosphatidylinositol (GPI) anchor, N-glycan precursor, protein O-mannose, and C-mannose. The enzyme has three subunits, DPM1, DPM2 and DPM3. DPM is synthesized from dolichol phosphate and GDP-Man on the cytosolic surface of the ER membrane by DPM synthase and then is flipped onto the luminal side and used as a donor substrate. This protein family belongs to Glycosyltransferase 2 superfamily.	2.15998e-97
NZ_CP024595.1\|WP_099779077.1\|274612_276070_-\|internalin	gnl\|CDD\|380191	NF033187, internalin_J, class 1 internalin InlJ. Internalins, as found in the intracellular human pathogen Listeria monocytogenes, are paralogous surface-anchored proteins with an N-terminal signal peptide, leucine-rich repeats, and a C-terminal LPXTG processing and cell surface anchoring site. See PMID:17764999 for a general discussion of internalins. Members of this family are internalin J (InlJ).	1.79016e-35
NZ_CP024595.1\|WP_004584814.1\|251449_252352_-\|glutamate-formimidoyltransferase	gnl\|CDD\|226169	COG3643, COG3643, Glutamate formiminotransferase [Amino acid transport and metabolism].	1.57335e-150
NZ_CP024595.1\|WP_004584826.1\|266437_267637_-\|methionine-gamma-lyase	gnl\|CDD\|168478	PRK06234, PRK06234, methionine gamma-lyase; Provisional.	0
NZ_CP024595.1\|WP_099779074.1\|267799_269269_-\|metallophosphoesterase-family-protein	gnl\|CDD\|277318	cd00839, MPP_PAPs, purple acid phosphatases of the metallophosphatase superfamily, metallophosphatase domain. Purple acid phosphatases (PAPs) belong to a diverse family of binuclear metallohydrolases that have been identified and characterized in plants, animals, and fungi. PAPs contain a binuclear metal center and their characteristic pink or purple color derives from a charge-transfer transition between a tyrosine residue and a chromophoric ferric ion within the binuclear center. PAPs catalyze the hydrolysis of a wide range of activated phosphoric acid mono- and di-esters and anhydrides. PAPs are distinguished from the other phosphatases by their insensitivity to L-(+) tartrate inhibition and are therefore also known as tartrate resistant acid phosphatases (TRAPs). While only a few copies of PAP-like genes are present in mammalian and fungal genomes, multiple copies are present in plant genomes. PAPs belong to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	4.78057e-14
NZ_CP024595.1\|WP_004584829.1\|269965_270571_+\|YihA-family-ribosome-biogenesis-GTP-binding-protein	gnl\|CDD\|234770	PRK00454, engB, GTP-binding protein YsxC; Reviewed.	2.70082e-98
NZ_CP024595.1\|WP_099779658.1\|276634_278077_+\|exo-alpha-sialidase	gnl\|CDD\|271234	cd15482, Sialidase_non-viral, Non-viral sialidases. Sialidases or neuraminidases function to bind and hydrolyze terminal sialic acid residues from various glycoconjugates, they play vital roles in pathogenesis, bacterial nutrition and cellular interactions. They have a six-bladed, beta-propeller fold with the non-viral sialidases containing 2-5 Asp-box motifs (most commonly Ser/Thr-X-Asp-[X]-Gly-X-Thr- Trp/Phe). This CD includes eubacterial and eukaryotic sialidases.	2.92922e-91
NZ_CP024595.1\|WP_005873836.1\|270580_271609_+\|UDP-glucose-4-epimerase-GalE	gnl\|CDD\|187558	cd05247, UDP_G4E_1_SDR_e, UDP-glucose 4 epimerase, subgroup 1, extended (e) SDRs. UDP-glucose 4 epimerase (aka UDP-galactose-4-epimerase), is a homodimeric extended SDR. It catalyzes the NAD-dependent conversion of UDP-galactose to UDP-glucose, the final step in Leloir galactose synthesis. This subgroup has the characteristic active site tetrad and NAD-binding motif of the extended SDRs. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	0
NZ_CP024595.1\|WP_005873802.1\|273747_274518_+\|HAD-IA-family-hydrolase	gnl\|CDD\|223710	COG0637, COG0637, Predicted phosphatase/phosphohexomutase [General function prediction only].	1.15004e-37
NZ_CP024595.1\|WP_099779076.1\|271651_273748_+\|ATP-dependent-DNA-helicase-RecG	gnl\|CDD\|236794	PRK10917, PRK10917, ATP-dependent DNA helicase RecG; Provisional.	0
NZ_CP024595.1\|WP_099779072.1\|260524_264052_+\|hypothetical-protein	gnl\|CDD\|380475	cd20477, Cas13b_Pb-like, Class 2 type VI-B CRISPR-associated RNA-guided ribonuclease Cas13b from Prevotella buccae and similar Cas13b proteins. CRISPR-Cas (clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins) adaptive immune systems defend microbes against foreign nucleic acids via RNA-guided endonucleases. These systems are divided into two classes: class 1 systems utilize multiple Cas proteins and CRISPR RNA (crRNA) to form an effector complex while class 2 systems employ a large, single effector with crRNA to mediate interference. Class 2 type VI CRISPR-Cas13 systems use a single enzyme to target RNA using a programmable crRNA guide and are divided into four subtypes based on the identity of the Cas13 protein (Cas13a-d). The Cas13 proteins are capable of both pre-crRNA processing and target RNA cleavage, which protect the host from phage attacks. Once bound to a target RNA, their non-specific RNase activity is activated. Cas13b has many distinctive features compared to the other Cas13 proteins, including the lack of significant sequence similarity, disparate crRNA repeat region, and double-sided protospacer flanking sequence (PFS)-dependent target RNA cleavage.	0

>NZ_CP024595.1|WP_097637689.1|264056_264602_+|hypothetical-protein
MMTMTICWTPICVQLIELSGIFIAAYLAYRYAVRKLSKESIENIERCKYQAVLEAHRSFYKLLRFTTDTENADSILVWQKAKGGGAKTYYFRPACIRGFLSELTDEFYKNGNGIFLSKEIISRIFEYRSIVYGLLLSERQNSDERIVMNKPETAERMISIHQELTQTVREAIALKKRTLNF
>NZ_CP024595.1|WP_099779072.1|260524_264052_+|hypothetical-protein
MTEQNEKPYNGTYYTLEDKHFWAAFFNLARHNAYITLAHIDRQLAYSKADITNDEDILFFKGQWKNLDNDLERKARLRSLILKHFSFLEGAAYGKKLFESQSSGNKSSKKKELTKKEKEELQANALSLDNLKSILFDFLQKLKDFRNYYSHYRHPESSELPLFDGNMLQRLYNVFDVSVQRVKRDHEHNDKVDPHRHFNHLVRKGKKDRYGNNDNPFFKHHFVDREGTVTEAGLLFFVSLFLEKRDAIWMQKKIRGFKGGTETYQQMTNEVFCRSRISLPKLKLESLRTDDWMLLDMLNELVRCPKSLYDRLREEDRARFRVPVDILSDEDDTDGAEEDPFKNTLVRHQDRFPYFALRYFDLKKVFTSLRFHIDLGTYHFAIYKKNIGEQPEDRHLTRNLYGFGRIQDFAEEHRPEEWKRLVRDLDYFETGDKPYITQTTPHYHIEKGKIGLRFVPEGQHLWPSPEVGATRTGRSKYAQDKRFTAEAFLSVHELMPMMFYYFLLREKYSDEASAERVQGRIKRVIEDVYAVYDAFARGEIDTLDRLDACLADKGIRRGHLPRQMIAILSQEHKDMEEKVRKKLQEMIADTDHRLDMLDRQTDRKIRIGRKNAGLPKSGVIADWLVRDMMRFQPVAKDTSGKPLNNSKANSTEYRMLQRALALFGGEKERLTPYFRQMNLTGGNNPHPFLHETRWESHTNILSFYRSYLKARKAFLQSIGRSDRVENHRFLLLKEPKTDRQTLVAGWKGEFHLPRGIFTEAVRDCLIEMGYDEVGSYKEVGFMAKAVPLYFERACKDRVQPFYNYPFNVGNSLKPKKGRFLSKEKRAEEWESGKERFRDLEAWSQSAARRIEDAFAGIENASRENKKKIEQLLQDLSLWKAFESKLKVKADKINIAKLKKEILEAKEHPYHDFKSWQKFERELRLVKNQDIITWMMCRDLMEENKVEGLDTGTLYLKDIRTDVHEQGSLNVLNRVKPMRLPVVVYRADSRGHVHKEQAPLATVYIEERDTKLLKQGNFKSFVKDRRLNGLFSFVDTGALAMEQYPISKLRVEYELAKYQTARVCAFEQTLELEESLLTRYPHLPDKNFRKMLESWSDPLLDKWPDLHRKVRLLIAVRNAFSHNQYPMYDEAVFSSIRKYDPSSPDAIEERMGLNIAHRLSEEVKQAKEMAERIIQA
>NZ_CP024595.1|WP_077083535.1|259667_260237_-|hypothetical-protein
MVFNFLIVSDEVEDFRREIAIDSEATFLDLQNAILDSVGYSHSELTSFFLCDEDWHKGQEITLMEMDTASDEDSYVMENTRLEEFIEDEHQRLVFEFDLMTERYFFIEVMDIVPGKSLSEPKLLTSEGLPPQQSSLDDLMDPTAIPTKQAKGLDLEEDFFGDSEYNEDEIDREGFEGFDEITSDLSDNY
>NZ_CP024595.1|WP_099779071.1|258749_259652_-|tRNA-(adenosine(37)-N6)-dimethylallyltransferase-MiaA
METQDHTLYVLLGPTGVGKTDLSLDIAERLGSPIISADSRQIFRELPIGTAAPTPEQRAKVPHLFVGTHSVRDYYSAGMYEVEVLEALKELFRKYRGVLLTGGSMMYIDAVCRGIDDIPDPFPEVREELYARYAAEGLDGILAQLRLLDPDYYAKVDRRNYKRVIHGLEICLSTGRPFSSFHRHEAKERPFRIVKIGLYREREELCRRIDARVLEMMEQGLEEEARAVYPLRHLNALNTVGYKEMFEYFDGSIDRAEAVRRIQRNSRVYARKQMTWFRRDSTIRWFHPEADKGTVLTLVT
>NZ_CP024595.1|WP_099779070.1|257737_258697_-|glycosyltransferase-family-2-protein
MDVNTTYTKELSIVVPIYNEEKGIPELVRRLSAAAASITEDYELIFVNDGSRDGSMELLRSLCKGDDRFFYINLSRNFGHQIAVSAGLDHVRGKATVIIDGDLQDPPELIPELYAKYREGYEVVYAQRKHREGETWFKKATAKGFYRTMRKITSIDMPLDTGDFRLIDQKIVQCLREMPEQNKFLRGQIAWMGFRQTGVQFDRDERKYGQTNYPLRKMLALAIDGITGFSSRPLEWVAQLGAWVSLLSLFVIVYALISHFLLNKTVSGWTSVIVSSMFLGGVQLICLGVIGTYISKINKNIVARPLYLVAESNIAADER
>NZ_CP024595.1|WP_099779069.1|256818_257727_+|DMT-family-transporter
MTSSRLYGLAVGILSSATFGLIPLFTLPVSAKGASFELILFYRFFFAAIAIGILHRLSGGSFKVSRADIGPLVLLGFLYAGTALFLFHGYGYMASGVATTIHFLYPLFVTALMLLFFGERLSPVPLTAIFIALIGVGLLMGLTGGGDRVGLTGFVIVAISALCYALYIVFVNRSRIRIMPGRRLTFYVFVAAAGFCLINILVRQGEVAPLPDAASWGNILLLALVPTVISNLALVVAVRNIGSTLTSALGAMEPLTSVLVGVWVFDEVLGASAIVGMGCILIAVGLIVFSEPLELMLRRRRR
>NZ_CP024595.1|WP_097637691.1|254614_256591_+|transcription-termination-factor-Rho
MQKYTIVDLNEKAEAELAAIAGELGIANAGSMPKQELIYKILDEQAISVAGVRKEKQKTTEDRHTERRKPGRPRKNAEEEAPESEDAAAAPAEPNDEEAQAKRKRGRPRKAAEEIAEETREDVQQLVALAAAEETNATEKESAGRKPAAKTSTASPAKAPAKALPRPAETTPRVAPSPPPTTPVSEPAKDDAKPETPAPPPAIESITTTPTAGAVDEGGARRLVFRHKNSSSVLDQVLPYSSPQPPQRPKPAGAPVGSSPIRQRQPAGVPTPRREPQQPLYNFDGILECMGVLEIMPDGYGFLRSSDYNYLSSPDDVYVSQQQIKHNGLKTGDVVAGTIRPPREGEKYFPFVQLRSVNGRSPEEIRDRVPFDHLTPLFPEEKFTLEAPGIRAVNDKISVRVVDLFAPIGKGQRGLIVSQPKTGKTMLLKDIANAIAANHPEVYMIVLLIDERPEEVTDMARSVNAEVIASTFDEPAERHVKIAEIVLNKAKRMVECGHDVVILLDSITRLARAYNTVQPASGKVLSGGVDANALQKPKRFFGAARNIENGGSLTILATALTDTGSKMDEVIFEEFKGTGNMELQLDRRLSNKRIFPAVDIMSSSTRRDDLLQDETTLNRMWILRKYLSDMNPVEAMEFVRKQLENTHTNMEFLASMSN
>NZ_CP024595.1|WP_021664582.1|253420_253939_-|DUF4496-domain-containing-protein
MSLKYVIKKSVAKIGPKAGQTIYYAQPAAQDSVTFHSLCKRIAEESALTSADVKGILDRLVNILSEELPNGKTVRIGELGSFRLSFGSKQLDDPKNFSVDQIQKHRLVFIPSAELKSIPARGKLRPGSSALAFDYERVEPQPKKKPGTGDNQTPSPSTPDGGGGQGGTGGGL
>NZ_CP024595.1|WP_021676668.1|252392_253388_-|hypothetical-protein
MFRISRLGIVLLVSLIACNLSKAQNTTKDLINLSIKYLEQNDSTAFRKTYQDIFMQYVTEALCAPFDKAIQDRDQTYIQARLDSLTSDPEEDAFTYHLLSKPEYQAFYYTLPRWEVYKSWIDSVERNPHADMRNEIWQIQREDQGIRILWLRLPNETGDNIRKKVRDEILLVDRQNTERAIHIIDTFGEWPGANRLGCSADQTLWLCIQHADQRPEVATRYLPMLQKAVEEKRTDPMHYAYLVDRIRMHECKEQIYGTQTYHVKEENGNKFFFVIPIEDIDHVDERRAGIGMDPLSDYVNSMGYDWDIRQYKKDLPKIWKYYRHSCEKKKN
>NZ_CP024595.1|WP_004584814.1|251449_252352_-|glutamate-formimidoyltransferase
MALSRIMECVPNFSEGRDKEKIEKIVNPFRTREGVKLLNYSNDEDHNRLVVTVVGEPEPLREAVLEAVGIAVELIDLTKHTGQHPRMGAVDVIPFIPIKNVTAEDADALAKEVGRTIGEKYGVPVFLYEKSATAPHRENLAKIRKGEFEGMAEKIHEADWHPDFGPADRHPTAGTVAVGARMPLVAYNVNLNTNDLSIADAIAKKVRFLGGGLRFCKAMGVELTDRGIVQVSMNLTDFTKTAVYRAHEMVRMEAARYGVSVVGSEVIGLVPMQALIDCAEYYLGIENFSMDQILESRIME
>NZ_CP024595.1|WP_004584826.1|266437_267637_-|methionine-gamma-lyase
MKKEDLMRSGFATRAIHGGAIENAFGCLATPIYQTSTFVFDSAEQGGRRFAGEEDGYIYTRLGNPNCTQVEEKLAMLEGGEAAASASSGIGAISSAIWVCVKAGDHIVAGKTLYGCTFAFLTHGLSRYGVEVTLVDTRHPEEVEAAIRPNTKLVYLETPANPNMYLTDIKAVCDIAHKHEGVRVMVDNTYCTPYICRPLELGADIVVHSATKYLNGHGDVIAGFVVGKEDYIKEVKLVGVKDLTGANMSPFDAYLISRGMKTLQIRMEQHCRNAQTVAEFLEKHPAVEAVYFPGLPSFPQYELAKKQMALPGAMIAFEVKGGCEAGKKLMNSLHLCSLAVSLGDTETLIQHPASMTHSPYTPEERAASDISEGLVRLSVGLENVEDIIADLKHGLDSLI
>NZ_CP024595.1|WP_099779074.1|267799_269269_-|metallophosphoesterase-family-protein
MRKKRSNPYYKVSRRKFSKRNSGRRYSRKRRRNGRRWGLMISLLLLVALGIWIAKRYRAWFVSPTEVAYTVPHTIDRLTLTPGEDFLTQRTVSWRCDTLPQDSWLDYRSPDGADADTLLISLPAEGKEVLTRAGRNYYYHAKINGLKPGRTYTYRVKTGEQTSPWYRFSIPDSSAATDFIYIGDVQDPGNGGSQALLQRLRTLHPHPDFLALGGDQIEGPTDFYWEVWHRVIGDWTASTPVIAATGNHEYIKGLKRQLDPRWVPQYNYPANGPKGFERRSYYIDFPHMRLIVMDTNDIQWPASVFNHRTWLKNALETTVQPWKVVMFHHGVYSVRQGRMNPIIRYGFRSILEEGGADLVLQGHDHAYSRITTKTESGTKTTPVYIISSASPKHYRNGFSEQHDRIGSGLYLYQTIHVTQGEIRYRSTTFDNRPYDDLHLKKQGGRTTVKDNAEDWKEIFAFDNFADSKKGRKKRADYRQAAQERAAGHR
>NZ_CP024595.1|WP_099779075.1|269271_269865_-|hypothetical-protein
MNKSLIILIYTLVWVLLIVLQSLALESANPGTPSFWNTPSAYYSIWIVDAYIIALYYINYFLIAPFMIKRHLFRPYIVLSLALGGIGMLLPVVFHHAWQWTIPGTSEGQMPLYGEGFIASIAAIAVGLSVRGVREWVRLARRNTNLEIALKNKSIAYDRAEARLRSLEQPVSFHNPGTGAKAENAPSSTPVSPQTNE
>NZ_CP024595.1|WP_004584829.1|269965_270571_+|YihA-family-ribosome-biogenesis-GTP-binding-protein
MEIKKAAFVISNTDVRKCPDTRLPEYAFIGRSNVGKSSLINMLTGQKGLAMTSQKPGKTQLINHFIIDDSWYLVDLPGYGYARLGASNRESLRRIIETYILCREQLSSLFVLIDCRHEPQKIDLEFLQWLGENGIPFGIVFTKADKLSFSRLKENTEAYKQKLLETWEELPPVFITSSEKKTGKEELLDYIDSINQELATK
>NZ_CP024595.1|WP_005873836.1|270580_271609_+|UDP-glucose-4-epimerase-GalE
MKQKILVTGGTGYIGSHTTVELQQAGYRVVSVDNFSNSNAAVLDGIARITGVRPDFYEADCNDTEAMERVFTAHPDIAGVIHFAASKAVGESVQKPLLYYRNNILSLLNILELMERFGTRGIVFSSSCTVYGQPEVLPVTEEAPIQEALSPYGNTKQINEEIIRDAIHAGAGYKAILLRYFNPIGAHPTAHIGELPNGVPQNLIPYLTQTAAGIRAELSVFGDDYDTPDGSCIRDYIYVVDLAKAHVAAIERMLNEEKASDSLEVFNIGTGRGVSVLELIRTFERVTGVAVPHRIVGRREGDIEQVWAEPKKANEVLGWKALESLEDTLLSAWRWQQRLSEK
>NZ_CP024595.1|WP_099779076.1|271651_273748_+|ATP-dependent-DNA-helicase-RecG
MDILSTKITYLTGVGPKRAEVLKEEIEVRTYLDLLHYFPFRYVDRSRFYAIREIRSDMPYIQLRGVLRNFSEVGEGRRKRLTATFSDGTGSIELVWFKGIKYIRDKLQEGRRYIVFGKPVFFASGYNIAHPEIDAEEKAERVAGGLTPIYHTTERMKSMGLGSKQLQQLLYVLLNQVSATLTETLPPYILSSYGFVSYQEAIRQIHFPQGVAQLEAARTRLKFEELFYVQLHLIGSKLERKARFQGIVFAQVGALFNTFYKEHLLFELTGAQKRVVREIRQDTLSGHQMNRLVQGDVGSGKTLVALLSMLLALDNGCQACLMAPTEILARQHHHTLSELLRPLGIEVGLLIGSCTARQRERLLPRLADGSLSIVVGTHALLEQGVAFRRLGMAVIDEQHRFGVQQRARLWEKNLDTLPHILIMSATPIPRTLAMTLYGDLDISVIDELPPGRKPIQTLHHFDNDMAPVFRFLRSQLAAGRQVYVVYPMIEGSETTDLKNLEDGFELFSSIFPDEGVTMVHGKMKAKEKEARMADFVSGRSRILLATTVIEVGVNVPNATVMVVENADRFGLSQLHQLRGRVGRGGEQSYCILITGTKTGEDSRRRIQVMVETNDGFEIAEEDMRLRGFGDLEGTRQSGRQISLRIANPARDTELIALSRSIAEQLLERDPELRHPDNQMLALRLNKLFPKEEDWSVIS
>NZ_CP024595.1|WP_005873802.1|273747_274518_+|HAD-IA-family-hydrolase
MEKKESMDYNNITEALQAFRTEKAYRHAPLRSCFFDMDGVLFDSMPAHARSWVEAAGECGIAAEPLDFYRWEGQKGSDTIKILFERGYGRLPTEKEIADMYGRKSQLFALYNSGNVIDDAPALVSDVCDRGLRIMLVTGSSQTDILQRLQRSYGDNFSPANMVTGADVHRGKPHPEPYLKALECVGMSPSEAFVVENAPLGVRAAVDAGIFTIAVNTGCLPDADLWDAGASLVLPSMAVLRSLLGELLTESLSSSA
>NZ_CP024595.1|WP_099779077.1|274612_276070_-|internalin
MKRKPLFSALVILSGFFGSVHPASAQKVPAPVDGERIIMELSEADVECTIKIEAEDGYANDIWADLNGNGKYDSGERLDSGEFRDVEFRQTKAIVYGKMAKFLFRGSSAGDYGATFIDISNCTGLTAFDCFANLLTELDLSKANGLTFVNCGKNQLTKLDLPANADIETLNCSKNKITSLNLSTYTKLKELYVGDNGLTALDLSANTLLEELVYSNNEVTTINLSANTNLKSLYCINNKMTGLDVAANKELKILHCNNNQLTALNLSANTKLTTLSFFNNELTNIDLSGNTALEWLFCNGNKLTKLDVSANANLIALQCSNNQLTALDLSKTPKLTTLNCYSNRIKDTAMRALIESLPTITEGEGRFVPYNDDEEGGEEENVCTTEHVEMAKAKNWKVLTSWGEPFPGITALISIEGESEYSVYAQDGILYLSGMEQGLPVQVYTMGGSMMYSSVASGSAMEIQLPRGAAYVVRIGSHAIKTAMP
>NZ_CP024595.1|WP_099779658.1|276634_278077_+|exo-alpha-sialidase
MYRTLVKVALSESLPPDAKQIRIGFSLPKETEEKVTALYLLVSDSLAVRDLPDYKGRVSYDSFPISKEDRTTALSADLVAGRRFFYLAADIGPVASFSRSDTLTARVEEVAVDGRPLPLKELSPASRHLYRGYEALFVPGDGGSRNYRIPAILKTANGTLIAMADRRKYNQTDLPEDIDIVMRRSTDGGKSWSDPRIIVQGEGRNHGFGDVALVQTQAGKLLMIFVGGVGLWQSTPDRPQRTYISESRDEGLAWSPPRDITHFIFGKDCADPGRSRWLASFCASGQGLVLPSGRITFVAAIRESGQEYVLNNYVLYSDDEGDTWHLSDCAYRRGDEAKLSLMPDGRVLMSVRNQGRQESRQRFFALSSDDGLTWERAKQFEGIHDPGCNGAMLQVKRNGRDQVLHSLPLGPDGRRDGAVYLFDHTSGRWSAPVVVNSGSSAYSDMTLLADGTIGYFVEEGDEISLVFIRFVLDDLFDARQ
>NZ_CP024595.1|WP_021678157.1|278141_278327_-|DUF1661-domain-containing-protein
MPEFSCLQFGKTWCVNFFALAREIKKSRTKTKKFRHHLLQKRRAAIRGFSARIGGIAVDGY

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Crispr_ID: NZ_CP024595_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024595_2

521650-521744

Orphan

Consensus_repeat	Method
GAAGCTCTCTTTTTGTCTCTTTCAGACT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP024595_2

>merge|NZ_CP024595|2|521650-521744|CRISPRCasFinder
GAAGCTCTCTTTTTGTCTCTTTCAGACTAGCAAAAACAGGGTTCTCAATTCCAAACAAATATCTGATGAAGCTCTCTTTTTGTCTCTTTCAGACT

>NZ_CP024595|2|2|521650-521744|CRISPRCasFinder
GAAGCTCTCTTTTTGTCTCTTTCAGACT	AGCAAAAACAGGGTTCTCAATTCCAAACAAATATCTGAT
GAAGCTCTCTTTTTGTCTCTTTCAGACT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024595.1\|WP_061156813.1\|510032_513614_+\|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase	unknown	unknown	gnl\|CDD\|131231
NZ_CP024595.1\|WP_021664688.1\|527335_527839_-\|DNA-binding-protein	unknown	unknown	gnl\|CDD\|273496
NZ_CP024595.1\|WP_099779139.1\|520482_521157_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_077492170.1\|530824_531838_+\|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|237845
NZ_CP024595.1\|WP_077492131.1\|525517_527194_+\|putative-transporter	unknown	unknown	gnl\|CDD\|179654
NZ_CP024595.1\|WP_010956062.1\|505154_505454_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_077492169.1\|529072_530629_-\|lamin-tail-domain-containing-protein	unknown	unknown	gnl\|CDD\|376421
NZ_CP024595.1\|WP_077082881.1\|519507_520410_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779142.1\|528374_528941_-\|elongation-factor-P	unknown	unknown	gnl\|CDD\|234788
NZ_CP024595.1\|WP_099779140.1\|521755_522577_-\|purine-nucleoside-phosphorylase-I,-inosine-and-guanosine-specific	unknown	unknown	gnl\|CDD\|273764
NZ_CP024595.1\|WP_099779136.1\|506657_507293_-\|terminase	unknown	unknown	gnl\|CDD\|313962
NZ_CP024595.1\|WP_099779135.1\|505867_506542_+\|integrase-catalytic-domain-containing-protein	unknown	unknown	gnl\|CDD\|271185
NZ_CP024595.1\|WP_097596496.1\|517893_518412_-\|histidinol-phosphate-phosphatase	unknown	unknown	gnl\|CDD\|273496
NZ_CP024595.1\|WP_097596500.1\|522596_523871_-\|amidohydrolase	unknown	unknown	gnl\|CDD\|238623
NZ_CP024595.1\|WP_021663920.1\|532520_533456_+\|16S-rRNA-(cytosine(1402)-N(4))-methyltransferase-RsmH	unknown	unknown	gnl\|CDD\|234597
NZ_CP024595.1\|WP_099779137.1\|507368_507839_-\|histidinol-phosphate-phosphatase	unknown	unknown	gnl\|CDD\|375718
NZ_CP024595.1\|WP_099779138.1\|514545_517368_-\|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|275036
NZ_CP024595.1\|WP_004585089.1\|508662_509844_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|379049
NZ_CP024595.1\|WP_099779141.1\|527861_528077_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_077492129.1\|523945_525301_-\|dipeptidase	unknown	unknown	gnl\|CDD\|349929

Protein	Function_ID	Function_description	E-value
NZ_CP024595.1\|WP_061156813.1\|510032_513614_+\|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase	gnl\|CDD\|131231	TIGR02176, pyruvate_flavodoxin/ferrodoxin_oxidoreductase, pyruvate:ferredoxin (flavodoxin) oxidoreductase, homodimeric. This model represents a single chain form of pyruvate:ferredoxin (or flavodoxin) oxidoreductase. This enzyme may transfer electrons to nitrogenase in nitrogen-fixing species. Portions of this protein are homologous to gamma subunit of the four subunit pyruvate:ferredoxin (flavodoxin) oxidoreductase.	0
NZ_CP024595.1\|WP_021664688.1\|527335_527839_-\|DNA-binding-protein	gnl\|CDD\|273496	TIGR01201, HU_rel, DNA-binding protein, histone-like, putative. This model describes a set of proteins related to but longer than DNA-binding protein HU. Its distinctive domain architecture compared to HU and related histone-like DNA-binding proteins justifies the designation as superfamily. Members include, so far, one from Bacteroides fragilis, a gut bacterium, and ten from Porphyromonas gingivalis, an oral anaerobe. [DNA metabolism, Chromosome-associated proteins].	3.20735e-63
NZ_CP024595.1\|WP_077492129.1\|523945_525301_-\|dipeptidase	gnl\|CDD\|349929	cd05680, M20_dipept_like, uncharacterized M20 dipeptidase. Peptidase M20 family, unknown dipeptidase-like subfamily (inferred by homology to be dipeptidases). M20 dipeptidases include a large variety of bacterial enzymes including cytosolic nonspecific dipeptidase (CNDP), Xaa-methyl-His dipeptidase (anserinase),and canosinase. These dipeptidases have been shown to act on a wide range of dipeptides, but not larger peptides. For example, anserinase mainly catalyzes the hydrolysis of N-alpha-acetylhistidine while carnosinase degrades beta-alanyl-L-histidine.	0
NZ_CP024595.1\|WP_077492170.1\|530824_531838_+\|aspartate-semialdehyde-dehydrogenase	gnl\|CDD\|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	1.34109e-179
NZ_CP024595.1\|WP_077492169.1\|529072_530629_-\|lamin-tail-domain-containing-protein	gnl\|CDD\|376421	pfam00932, LTD, Lamin Tail Domain. The lamin-tail domain (LTD), which has an immunoglobulin (Ig) fold, is found in Nuclear Lamins, Chlo1887 from Chloroflexus, and several bacterial proteins where it occurs with membrane associated hydrolases of the metallo-beta-lactamase,synaptojanin, and calcineurin-like phosphoesterase superfamilies.	2.4661e-06
NZ_CP024595.1\|WP_097596500.1\|522596_523871_-\|amidohydrolase	gnl\|CDD\|238623	cd01298, ATZ_TRZ_like, TRZ/ATZ family contains enzymes from the atrazine degradation pathway and related hydrolases. Atrazine, a chlorinated herbizide, can be catabolized by a variety of different bacteria. The first three steps of the atrazine dehalogenation pathway are catalyzed by atrazine chlorohydrolase (AtzA), hydroxyatrazine ethylaminohydrolase (AtzB), and N-isopropylammelide N-isopropylaminohydrolase (AtzC). All three enzymes belong to the superfamily of metal dependent hydrolases. AtzA and AtzB, beside other related enzymes are represented in this CD.	1.79943e-162
NZ_CP024595.1\|WP_099779142.1\|528374_528941_-\|elongation-factor-P	gnl\|CDD\|234788	PRK00529, PRK00529, elongation factor P; Validated.	2.9716e-99
NZ_CP024595.1\|WP_099779140.1\|521755_522577_-\|purine-nucleoside-phosphorylase-I,-inosine-and-guanosine-specific	gnl\|CDD\|273764	TIGR01700, Purine_nucleoside_phosphorylase_1, purine nucleoside phosphorylase I, inosine and guanosine-specific. This model represents a family of bacterial and metazoan purine phosphorylases acting primarily on inosine and guanosine and not acting on adenosine. PNP-I refers to the nomenclature from Bacillus stearothermophilus where PHP-II refers to the nucleotidase acting on adenosine as the primary substrate.The bacterial enzymes (PUNA) are typified by the Bacilus PupG protein, which is involved in the metabolism of nucleosides as a carbon source.Several metazoan enzymes (PNPH) are well characterized including the human and bovine enzymes which have been crystallized. [Purines, pyrimidines, nucleosides, and nucleotides, Salvage of nucleosides and nucleotides].	2.9955e-155
NZ_CP024595.1\|WP_099779136.1\|506657_507293_-\|terminase	gnl\|CDD\|313962	pfam10899, AbiGi, Putative abortive phage resistance protein AbiGi, antitoxin. This is a bacterial family of proteins with unknown function. AbiGi is a family of putative type IV toxin-antitoxin system antitoxins. The AbiG abortive phage resistance system affects lactococcal bacteriophages phiP335 and phiQ30 but not the other P335 phage species. AbiGii toxin appears to confer resistance to phages by a mechanism of abortive infection that acts by interfering with phage RNA synthesis. The cognate toxin is found in pfam16873.	6.56209e-06
NZ_CP024595.1\|WP_099779135.1\|505867_506542_+\|integrase-catalytic-domain-containing-protein	gnl\|CDD\|271185	cd01185, INTN1_C_like, Integrase IntN1 of Bacteroides mobilizable transposon NBU1 and similar proteins, C-terminal catalytic domain. IntN1 is a tyrosine recombinase for the integration and excision of Bacteroides mobilizable transposon NBU1 from the host chromosome. IntN1 does not require strict homology between the recombining sites seen with other tyrosine recombinases. 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.	5.47579e-53
NZ_CP024595.1\|WP_097596496.1\|517893_518412_-\|histidinol-phosphate-phosphatase	gnl\|CDD\|273496	TIGR01201, HU_rel, DNA-binding protein, histone-like, putative. This model describes a set of proteins related to but longer than DNA-binding protein HU. Its distinctive domain architecture compared to HU and related histone-like DNA-binding proteins justifies the designation as superfamily. Members include, so far, one from Bacteroides fragilis, a gut bacterium, and ten from Porphyromonas gingivalis, an oral anaerobe. [DNA metabolism, Chromosome-associated proteins].	8.31535e-56
NZ_CP024595.1\|WP_021663920.1\|532520_533456_+\|16S-rRNA-(cytosine(1402)-N(4))-methyltransferase-RsmH	gnl\|CDD\|234597	PRK00050, PRK00050, 16S rRNA (cytosine(1402)-N(4))-methyltransferase RsmH.	1.39367e-142
NZ_CP024595.1\|WP_099779137.1\|507368_507839_-\|histidinol-phosphate-phosphatase	gnl\|CDD\|375718	pfam18291, HU-HIG, HU domain fused to wHTH, Ig, or Glycine-rich motif. Rapidly-diverging family of HU domains predominantly observed in the bacteroidetes lineage with a predicted role in recognition and possible interception of the DNA of parasitic elements, a counter-conflict strategy preventing incorporation of these elements into the host genome.	1.96282e-15
NZ_CP024595.1\|WP_099779138.1\|514545_517368_-\|T9SS-type-A-sorting-domain-containing-protein	gnl\|CDD\|275036	TIGR04183, hypothetical_protein, Por secretion system C-terminal sorting domain. Species that include Porphyromonas gingivalis, Fibrobacter succinogenes, Flavobacterium johnsoniae, Cytophaga hutchinsonii, Gramella forsetii, Prevotella intermedia, and Salinibacter ruber average twenty or more copies of a C-terminal domain, represented by this model, associated with sorting to the outer membrane and covalent modification.	8.73088e-06
NZ_CP024595.1\|WP_004585089.1\|508662_509844_+\|ATP-binding-protein	gnl\|CDD\|379049	pfam13173, AAA_14, AAA domain. This family of domains contain a P-loop motif that is characteristic of the AAA superfamily.	8.36193e-24
NZ_CP024595.1\|WP_077492131.1\|525517_527194_+\|putative-transporter	gnl\|CDD\|179654	PRK03818, PRK03818, putative transporter; Validated.	0

>NZ_CP024595.1|WP_099779139.1|520482_521157_+|hypothetical-protein
MNEVPVIRKGRLKSYWNTAFRGGFFLGLFVFLAALTKQSLLNSLLFGLMIWAFVIVLWLGVGFTSEEYYKRKKQIKKLMSDQYAFLDLHGFTLHEDLYFEGIYEGFFFRVCPATEYIKKGYAGKKAIEYVIIESFYRFASEATDMDREVKMSGEYNFGDVHFENHCAGFVPKDWKNPDFKASFDALITIFEREGLLPITKNDWESTFGQHSKKAKDASRKNPQR
>NZ_CP024595.1|WP_077082881.1|519507_520410_+|hypothetical-protein
MMKLSSGGVSSAVVNNGTIVQQAGFLPAGTTFFTPMVLFQITSFVTGQYYMNGMTKQLNAALEKLDTLIEFYYRERMAKIKQSVSLINKNLSNKIFSDEDLQQMKDVHSDLSIIKNEFFEDLSCMAREMSKKNKRNPWGKLKAAKSIEKEKAKFIHKMEILLFVEALLYLTKVTELYMNIRYIQPDMNRLNWTLSALIELSTFREDDLFSMELINLHETVKKEILEYLSDLEKGPIFTSKIREIKSNFENSFVDIEEHKDNLLSEAKEIHKSTLVRFEKDKMFVIDFRNGNLELYSSNDQ
>NZ_CP024595.1|WP_097596496.1|517893_518412_-|histidinol-phosphate-phosphatase
MIGYVSKQSKVANKDGKRVWYPQTVASGRVIDTKRVARELAARSGASEGDVHGILHDLGLVLRDYLSTGARVVLDGVGSFRITANARGKGVEKKEDVSPRQFNSIRVAFYPEKRVNQSTHTTNVTLIDPNLRFVYVKNPKDAAGNASSQTNTSDSPTPPNGGGEQGSQGGGL
>NZ_CP024595.1|WP_099779138.1|514545_517368_-|T9SS-type-A-sorting-domain-containing-protein
MNKFYKSLLQSGLAAFVSMATALTASAQISFGGEPLSFSSRSTETHSFDDAMTIRLTPDFNPEDLIAQSRWQSQRDGRPVRIGQVIPVDVDFASKALLISSIGDVDVYRLQFKLEGAKAITLYYDAFNIPEGGRLYIYTPDHEIVLGAYTNATHRRNGAFATEPVPGSELIMDYEVSRGGTLPDIKISGAGYIFDKVGGRPVTDNHYGIGEDDSDSDCEININCPEGADWQAEKNGVVQMIMVKGQYISMCSGNLLNNTKGDFTPLIISAGHCASLTTNFGVTQSELDKWIFTFHYEKRGCSNGTLAIFRGNSIIGASMKAFLPIKGKSDGLLLQLNDEVPLRYRVYYNGWDSTPDIPSSGAGIHHPAGDAMKISILKKTPTLNTWISSSGSGGTDDHFYFKYDQGGTEGGSSGSSLFNQNKHVVGTLTGGAGNCGGTEFYGRLNSHWNEYASDGNTSRMDIYLDPQNNGQTTVLNGTYRDGYKPLPSVPRLLLQSTGDQVELNWTAVPADQYPSSYQVEYHIFRNGKEIATTKELSYSDPIDESIIGSGIIRYEVSARFIYPSPLDGVESYKDTDKTSADLAIGDIQTKLKPDVTPLPGGGVSLSWKVPFLSQLVSRFGESPNPVFKTFEVPYVSAAAAQTPNPPVGVVIADKFMAGTYPEKAAIAAVYVMPSAPDSTFHLFLKSNTNRRLQKVTTPSDWQAGTWLRINLDKPFPVNNDHMLFAGIRMPNKYKLNRAIRYVRNPDNLFSITGKKISYNNGVSFEGYGIPSLLGYMAIKYLVVNTDAPKIDMSLVQEPYAKGTNVAPFPELVSIYVYKNGTFIGTQDPSVTTYSVSDGTESDEYEIKLVYKGSGISNGVAQIENNNAVVAYPSVVTDRFSIKNAHMVHAAALYSLDGKQVRSWNNLRNGVTFSVQGLTAGTYMLVMQTANGPVSQKIVKQ
>NZ_CP024595.1|WP_061156813.1|510032_513614_+|pyruvate:ferredoxin-(flavodoxin)-oxidoreductase
MAKEKKFLTCDGNQAAAHIAYMFSEVAAIYPITPSSTMAEYVDDWAAAGRKNIFGETVRVQEMQSEAGAAGAVHGSLQGGALTTTFTASQGLLLMIPNMYKIAGELLPCVFHVSARTIASHALSIFGDHQDVMAARQTGFAQLCTGSVQEVMDLAGVAHLATLRTRIPFIHFFDGFRTSHEIQKIEALDNEDLARFIDWDDVKRFRKQALNPESPVTRGTAQNGDIYFQNREACNRFYDAVPEAVQYYMDQLATVTGRHYHLFDYYGDPEAEHVIIAMGSVTEAIREVIDFLRAKGEKVGLLSVHLYRPFSAKHFLAAMPKTVKRIAVLDRTKEPGATGEPLYLDVRDCYYGMEDAPLIVGGRYGLSSKDTTPAQMKAVFDNLKLNVPKDHFTVGIVDDVTFTSLPLGEDLIFDNPSLVEAKFYGLGADGTVGANKNSVKIIGDNTNKYCQAYFAYDSKKSGGFTCSHLRFGDTPIRSTYLVVTPDFVACHVPAYLRMYDVLKGLKKKGTFLLNSIWAPEDIEQHLPNKVKRYLAKNNIRFYTINATAIAQQIGLGNRTNTILQSAFFKIANVIPYDLAVEQMKKFIVKSYGKKGEDVVNKNFAAVDRGGDVVEITVKSEWADLPDDPVVRHEGDTDFVHNVVRPINAQAGDDLPVSAFLGREDGTWDSGTAASEKRGVAAFVPVWEADNCVQCNQCAYVCPHATIRPFVLTKEEEEKTGVKVLKAVGKQFPDMGFRIQVNVMDCLGCSNCVDVCPGNKNGKALTMQPIEEQYEEQKNWDKMISGVTGKAHLVDIAANVKNSQFATPLFEFSGACSGCGETPYVKLITQLYGDRQTVANATGCSSIYSASAPSTPYTKNERGEGPAWANSLFEDNAEFGLGMHLAYKKMRRRLVNLAEEAQQSPCCSDELKALLREWVEKRQDAVASKVLADKIKPLVAACDCDICKRIGRVDSFFIKRAQWIIGGDGWAYDIGFGGLDHVIASGMNVNILVLDTEVYSNTGGQSSKSTPIGAIAKFAAAGKRIRKKDLGMIAATYGYVYVAQVSIGANPAQTLKAIREAEAYDGPSIVIAYSPCISHGIKSGMGKTQAEGKRAVECGYWHLWRYNPELEKEGKNPFQMDSKEPNWSEFKNFLKGEVRYASLYKEFPEDAEQLFDAAFENAQWRYRNYMRMSAADWSLPLGIQDIKEEKDRDH
>NZ_CP024595.1|WP_004585089.1|508662_509844_+|ATP-binding-protein
MNNFFKIHDNLLRNLSPSLRRGLMDEIDWNDRLIGIKGARGMGKTTFLLDYARENFGIGNRKCLYINLNQLYFTTESLVNFAGEFVKQGGEVLLLDQVFKYPNWSIELRQCMELYPDLRIVFTGSTVMRLKEENPELNGLVTSYVLNGFSFREFLNLKTGLSLQPYSFDEIVSNHEQIAPRILEQVNPLDWFQDYLHHGYYPIFLEDKNYSESLLKTLNMTLEVDVLFIRQIEQRFLHKLRKLLYLLGQRAPGSLNISSIAKEVDTSRTTITNYLKYLSEARLIKELHREEETGAKKPAMIYLDNTNVGYVIQPEPLNYIDVLKTFFLNQVKSRNEVCLGSRSQIAFCVNRQYQFCIDEKMSRRYRPDRYYAIQNMRSGTRNMIPLWLFGFLY
>NZ_CP024595.1|WP_099779137.1|507368_507839_-|histidinol-phosphate-phosphatase
MANKPLQFVLMERKMNVGPQAGKTVQVAHPTGRHRVDFRSFCERVAKSTTFNRQEVEAVLNYATEIARDIVANGDIVEFGDLGTLSPSFKSKIVPQGEVFNVQKHIEKPVVRLSPSKKYFTLTDVTYEQTVAKPKKGSTKPTPQPNEGGASNDEGL
>NZ_CP024595.1|WP_099779136.1|506657_507293_-|terminase
MNNRPDFSNYLVHFTKDNEPCGVKDPNNPIENKAKGEALTRLISILTDKKIIASTMPWTNCHCVCLTECPWSSLIDHTKSYSPYGIGFSKPFVFSRNGSPVYYVRADQYEKQQWHEHLHPFVTPFWPSYRAKSIEAKKKFQTCDYTHEREWRVPHDFPFEHDQIEFIILDKYEDMAKFPKELKDSIGRDKFLLMDNYKMIEKLWPVHNLGI
>NZ_CP024595.1|WP_099779135.1|505867_506542_+|integrase-catalytic-domain-containing-protein
MMDKHLCWLSRLMYRAVSQGTIRFNLFEEAKYEAVECKPRFLSKGDVAKLLAFPLQDEGAELSRRMFLFSIFTGLAFADLQSLRASQIEMNSEGKRYIRKARQKTEVESLIPLHPIAEQILSLYTKENSKGDYKIFPNMLSKSKLLTHLKAVGLACGIRTPLTYHMARHSFGTLTLEAGIPIESIAKMMGHSSIASTQIYAQITDQKIARDMDRLMQQCGCRLV
>NZ_CP024595.1|WP_010956062.1|505154_505454_+|hypothetical-protein
MEQKMIFITYNQAYHDIIIRLLSRYNLRGYTYWETVRGCGSDTGEPHLGTHAWPTLNGALMVVCPSEKMKTIMDALRILDAATPDQGLRAFVWNIEQTI
>NZ_CP024595.1|WP_099779140.1|521755_522577_-|purine-nucleoside-phosphorylase-I,-inosine-and-guanosine-specific
MKLQEQHYHEAASFLSSRLPGDAKTAIILGSGLGELAEKIENKTVIPYNEIPHFAQATAVGHKGNIIGGILGGTPVVAMQGRFHYYEGYSMDQVTFPIRVMKLLGIENLFVSNAAGGINTSFKVGDLMIICDHINNLPNPLIGPNMDMFGVRFPDMTRAYDREFIAKAKGIAQELNIPVKEGVYVGLTGPSYETPAEYKFWGQVGGDAIGMSTVPEVIVARHTGIRVFGMSVITNEGYHFADDFVNDEQDVIRAANAASKKMGAIFARLIAAV
>NZ_CP024595.1|WP_097596500.1|522596_523871_-|amidohydrolase
MGILIKQALLEGVRQDIRIEGNRIVEVAPAIGCHADEIIDASSMAVIPGLQNCHTHSAMTIFRGYGDDLRLMDWLENWIWPVEAQMTEEDVYWGSKLACLEMIKSGTTAFLDMYAHTLATARAVEEMGLRAVLSSTLFDRGDQERARIDRERCYSLHEAFCSYSDRIQFSVGPHAIYTVSGEQLQFCHRFANEKNVLIHLHLSETEGEVRDCIAKFGTTPVRYLHKLGVLSPQLILAHSIWLDDEEMDLLAAHGCKVVHNPASNMKLASGYRFHYDEMRKRGIVIGLGTDGCSSSNNLDMIIAMKLAAFLGKAWRSDATAVKATDIYESATADGARIMGTDAGVIAPGRLADLCLVRLDIPEMTPCHNFISNLVYSANGSAVDTTIVDGKILMRGRKVPGEEAILAGAAEAAYKLMAKAHKTHE
>NZ_CP024595.1|WP_077492129.1|523945_525301_-|dipeptidase
MNIRDYIRENEARFLEDLFALIRIPSVSAKSEHKPDMQRCAEHWRNHLLQVGAQKAEVFRTPGNPVVYAERIMDPKAKTILVYAHYDVMPPEPLELWKSEPFEPVIRDGHIWARGADDDKGQGMIQVKGFETALALGLVQCNVKFLFEGEEEIGSTNLEAFCRAHKEMLSADVIIVSDTSMVSAETPSLTTGLRGLAYWEMEVTGPNRDLHSGHFGGAVANPINELCKLIAGIVDENGRITIPHFYDDVVPLSDEERQMIAQVPFSEEKYCQALDIDAVFGEAGYSTLERNSCRPSFDVCGIWGGYTGEGAKTVLPSKAYAKVSSRLVANQDHEKISQMFIDYIRSVAPKHIKVKVTPLHGGEAYLCPIDLPAYKAAEEACTIAFGKRPLAVRRGGSIPIIATFEKVLGLKTVLMGFGLESNAIHSPNENMPLDIFRKGIESVAEFYRIYK
>NZ_CP024595.1|WP_077492131.1|525517_527194_+|putative-transporter
MDAIVLWLREVFLEPSVTQTIIILSLVCALGLQLGKLRIGTISLGITFVFFVGILASHFGVTADPVMLTFAQNFGLVIFVYALGLQVGPSFFPSLKKGGIAQNLISLGLVLLTFLLCILLYYILGISMPNLMGIVAGATTNTPALGAAQTTLHQINPDATAEMAEMALACAVTYPLGVVGVIIALAMLKVMMPKVEERDDSEAPKAFFSEYEICNPALDGKSVREVALLLKRPFVITRVWHNGKVEIPTSDMILYFGDHILAVSGEEDTSQLEILFGKREMKDWNRPDIDWNSVDKQLVSRRLVITRPKLNGVRLGMLKIRNLYGVNISRVDRAGVELLPDRDLRLQLGDRLTVVGEGKAVERVAEILGDEVKQLDNPHLTTLFGGLVLGCVFGMIPFYLPGVSMPIKLGLAGGPIIIGILMGAFGPRFHLTTYVTNSANLLLRQFGIILYLGGLGLASGANFFDTIIHGDGLLWVGTGFLITMLPTLLVGWASIKFLRNRYDGTAGMICGSTANPMALDYVNSQLKGDGASVVYATVYPLSMFVRIIFAQIMILIFA
>NZ_CP024595.1|WP_021664688.1|527335_527839_-|DNA-binding-protein
MLFFKRRQSCIAHKATGKKLWYPQTVINGSTASTLHIAEQISELSGASPGDVFGILRDLGIVMRRELASGKKIKLDGIGCFRLIAQAKGSGVEKKEDVKASQFNSVRVNFRAECRYNTVTRERDCTLIAPDLKFAEYGKPLPAGASANAGDSNSQTGGGDQGSGGGL
>NZ_CP024595.1|WP_099779141.1|527861_528077_-|hypothetical-protein
MLRSLCLRNTEAVLYIKRKAPFVVENFFPQNIWTIGFFTLIFAVQTERRGWRRIDLSIAIIKLMDRKSPHY
>NZ_CP024595.1|WP_099779142.1|528374_528941_-|elongation-factor-P
MATTADFRNGMCLEIEGQYYFIVEFLHVKPGKGPAFVRTKLKNVATGRILDKTWNSGVKVEEVRIERRPYQYLYQDEMGYNFMHPETFEQITIPGASIDGVQFLKDGDMVEAMVHATSETVLTCELPPHVKLRVTYTEPGLKGDTATNTLKPATVETGAEVRVPLFIQEGELIEVDTRDGSYTGRVKE
>NZ_CP024595.1|WP_077492169.1|529072_530629_-|lamin-tail-domain-containing-protein
MIRRLTVWLFLLSIVCPPLSAQWAENFDHITALTSPPWRGQIADFAIIKKQLKLYVEYPDDLNESRIAITVPYFKTTTWKGDVKLDFRPTVNNYLYCYLYCYGEISDSEFDYVALRWGSGSKGVDLLDVRLRVLPSGESSIVQSDILIDGSAYPLGTKPFTSFTVTYAVGSGWQLWVNGGNDTGNETVLIGSSSFDVESPFQSGGLGIDCFYTKSRSKAFSFDNLSVTEGTVSPPEEEEEPIPLGKPTLNELMANPLEGGSEYIELYNPTDKPVVPSKFAIGILRNGSYTTTTALPTVADTLYPGQYIVFARKSEGVTDFYPQAQNVVTMSNLPQLANKGFTLGLFEEGLDQPLEEVVYSPKMLGEGNVTRRGVSLERISFETPASDPTNWAGGLPSAGYATPGYLNSQSSNADTTQLGLPNNETEGNGKSYLPPASIAEEILLLPKGSLCGSAIYLMSAKTVKYMDGTATKRWCRKFSEGKDLGESMGLPSGYSYLIVVWIQRPDSMVYARKCIVTL
>NZ_CP024595.1|WP_077492170.1|530824_531838_+|aspartate-semialdehyde-dehydrogenase
MKIAIVGVSGAVGQEFLRVLSQRDFPIDGLYLFGSSRSAGSVYSFKGKEYVVRELKDNDDFKGIDIAFCSAGGDTSIAFADTITRHGTLMIDNSSAFRMQEDVPLVVPEVNGDDALVHPRNIISNPNCTTIQMVVALKPIEDLSHIRRVHVATYQAASGAGALGMAELVQQVEELARGEKPTVDKFAYQLMYNLIPQIDVFTDNDYTKEEMKMYRETKRIMHSDVMVSATCVRVPVMRAHSEAIWVETERPIAPEEARAAFAKAPGVLLCDEPSEKQYPMPLFGTEQDPVIVGRIRQDLANPNGLVFWCVSDQIRKGAALNAVQIAEYLIAKGHFAR
>NZ_CP024595.1|WP_021663920.1|532520_533456_+|16S-rRNA-(cytosine(1402)-N(4))-methyltransferase-RsmH
MHCPDKESVYHIPVMLGECLEGLRIDPDGCYVDVTFGGGGHSRAIVEKLSSKGRLYGFDQDADACRNILQDERFTFVTSNFRYLANFMDYYGEDGVDGILADLGVSSHHFDEEERGFSFRSESPLLDMRMNARAGRNAAAILNEYDASSLSALFYHYGELKQARRLAASIVHYRESLSGGLQTVGQLLEAVRGLISPREEKKQLACIFQALRIEVNDELGALQQMLEAALGCLRSGGRLVVMTYHSLEDRMVKNFLRYGTVKAPDEDSLRLYGAPQSPWQQITRKPLTASTKELSDNPRSRSAKLRIAEKI

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Crispr_ID: NZ_CP024595_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024595_3

1082408-1083036

TypeVI-B1,TypeVI-B2

VI-B1

Consensus_repeat	Method
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	PILER-CR
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CRISPRCasFinder
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CRT

9 spacers

cas13b,Csx27

The CRISPR arrays of NZ_CP024595_3

>merge|NZ_CP024595|3|1082408-1083036|PILER-CR,CRISPRCasFinder,CRT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACATTTTCAGTAAGATTAAAATGTTCTCTGTGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACCATGACGTTGTATTGCATCGACCGTATCGAGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACTGGGGAAACGCTCTGATAGGATCAGAATGTGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACTCATCAGGTGGTGATGATGTCTGGATTGCCGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACAAGGGCGAAACTGTACTCGACATCTGCAGCGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACTTTTTTGTTTTCATACTATGTATGTTTTTGGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACAGTTTGAATATAGACGGTTTTTTATCATTAGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACCTAACCCAAAGGCATAAGAGTTGGCGATTTGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAACGATAAATACTCTAAGTCTTCAGCCTCCTCTGTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC

>NZ_CP024595|3|2|1082408-1083036|PILER-CR
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	ATTTTCAGTAAGATTAAAATGTTCTCTGT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CATGACGTTGTATTGCATCGACCGTATCGA
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TGGGGAAACGCTCTGATAGGATCAGAATGT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TCATCAGGTGGTGATGATGTCTGGATTGCC
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	AAGGGCGAAACTGTACTCGACATCTGCAGC
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TTTTTTGTTTTCATACTATGTATGTTTTTG
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	AGTTTGAATATAGACGGTTTTTTATCATTA
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CTAACCCAAAGGCATAAGAGTTGGCGATTT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	GATAAATACTCTAAGTCTTCAGCCTCCTCT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC

>NZ_CP024595|3|3|1082408-1083036|CRISPRCasFinder
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	ATTTTCAGTAAGATTAAAATGTTCTCTGT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CATGACGTTGTATTGCATCGACCGTATCGA
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TGGGGAAACGCTCTGATAGGATCAGAATGT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TCATCAGGTGGTGATGATGTCTGGATTGCC
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	AAGGGCGAAACTGTACTCGACATCTGCAGC
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TTTTTTGTTTTCATACTATGTATGTTTTTG
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	AGTTTGAATATAGACGGTTTTTTATCATTA
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CTAACCCAAAGGCATAAGAGTTGGCGATTT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	GATAAATACTCTAAGTCTTCAGCCTCCTCT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC

>NZ_CP024595|3|2|1082408-1083036|CRT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	ATTTTCAGTAAGATTAAAATGTTCTCTGT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CATGACGTTGTATTGCATCGACCGTATCGA
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TGGGGAAACGCTCTGATAGGATCAGAATGT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TCATCAGGTGGTGATGATGTCTGGATTGCC
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	AAGGGCGAAACTGTACTCGACATCTGCAGC
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	TTTTTTGTTTTCATACTATGTATGTTTTTG
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	AGTTTGAATATAGACGGTTTTTTATCATTA
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	CTAACCCAAAGGCATAAGAGTTGGCGATTT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC	GATAAATACTCTAAGTCTTCAGCCTCCTCT
GTTGGGAATACCCTTAGTTAGAAGGGTGGAGACAAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024595.1\|WP_157766763.1\|1076508_1077093_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_004584374.1\|1091141_1091747_-\|DUF4254-domain-containing-protein	unknown	unknown	gnl\|CDD\|379447
NZ_CP024595.1\|WP_099779278.1\|1072739_1075412_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|236545
NZ_CP024595.1\|WP_099779284.1\|1092461_1093610_-\|iron-containing-alcohol-dehydrogenase	unknown	unknown	gnl\|CDD\|341466
NZ_CP024595.1\|WP_012458144.1\|1089566_1090019_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224108
NZ_CP024595.1\|WP_005873518.1\|1078279_1078996_+\|hypothetical-protein	Csx27	-	unknown
NZ_CP024595.1\|WP_058018901.1\|1091906_1092323_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_021664633.1\|1090002_1091058_-\|glycosyltransferase-family-9-protein	unknown	unknown	gnl\|CDD\|340821
NZ_CP024595.1\|WP_010956235.1\|1087671_1088682_+\|cobalamin-biosynthesis-protein-CobD	unknown	unknown	gnl\|CDD\|377002
NZ_CP024595.1\|WP_099779282.1\|1084598_1085165_+\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	unknown	unknown	gnl\|CDD\|376665
NZ_CP024595.1\|WP_004584294.1\|1068048_1068522_+\|PaaI-family-thioesterase	unknown	unknown	gnl\|CDD\|239527
NZ_CP024595.1\|WP_004584296.1\|1069222_1070590_-\|lactate-utilization-protein	unknown	unknown	gnl\|CDD\|224062
NZ_CP024595.1\|WP_099779281.1\|1083256_1084576_+\|cobyrinate-a,c-diamide-synthase	unknown	unknown	gnl\|CDD\|234896
NZ_CP024595.1\|WP_004584297.1\|1070586_1071408_-\|(Fe-S)-binding-protein	unknown	unknown	gnl\|CDD\|223325
NZ_CP024595.1\|WP_023846767.1\|1078992_1082400_+\|hypothetical-protein	cas13b	cas13b_CAS_V-B1	gnl\|CDD\|380475
NZ_CP024595.1\|WP_099779277.1\|1071647_1072520_-\|phosphoserine-phosphatase-SerB	unknown	unknown	gnl\|CDD\|319803
NZ_CP024595.1\|WP_099779279.1\|1075509_1076271_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779283.1\|1086650_1087658_+\|threonine-phosphate-decarboxylase	unknown	unknown	gnl\|CDD\|273466
NZ_CP024595.1\|WP_054190948.1\|1085161_1086658_+\|cobyric-acid-synthase	unknown	unknown	gnl\|CDD\|234838
NZ_CP024595.1\|WP_005873513.1\|1068632_1069217_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|224473

Protein	Function_ID	Function_description	E-value
NZ_CP024595.1\|WP_099779278.1\|1072739_1075412_-\|hypothetical-protein	gnl\|CDD\|236545	PRK09510, tolA, cell envelope integrity inner membrane protein TolA; Provisional.	1.33172e-05
NZ_CP024595.1\|WP_099779284.1\|1092461_1093610_-\|iron-containing-alcohol-dehydrogenase	gnl\|CDD\|341466	cd08187, BDH, Butanol dehydrogenase catalyzes the conversion of butyraldehyde to butanol with the cofactor NAD(P)H being oxidized in the process. The butanol dehydrogenase (BDH) is involved in the final step of the butanol formation pathway in anaerobic micro-organism. Butanol dehydrogenase catalyzes the conversion of butyraldehyde to butanol with the cofactor NAD(P)H being oxidized in the process. Activity in the reverse direction is 50-fold lower than that in the forward direction. The NADH-BDH has higher activity with longer chained aldehydes and is inhibited by metabolites containing an adenine moiety. This protein family belongs to the so-called iron-containing alcohol dehydrogenase superfamily. Since members of this superfamily use different divalent ions, preferentially iron or zinc, it has been suggested to be renamed to family III metal-dependent polyol dehydrogenases. This family also includes E. coli YqhD enzyme, an NADP-dependent dehydrogenase whose activity measurements with several alcohols demonstrate preference for alcohols longer than C3. The active site of YqhD contains a Zn metal, and a modified NADPH cofactor bearing OH groups on the saturated C5 and C6 atoms, possibly due to oxygen stress on the enzyme, which would functionally work under anaerobic conditions.	3.99853e-178
NZ_CP024595.1\|WP_012458144.1\|1089566_1090019_-\|hypothetical-protein	gnl\|CDD\|224108	COG1187, RsuA, 16S rRNA uridine-516 pseudouridylate synthase and related pseudouridylate synthases [Translation, ribosomal structure and biogenesis].	1.32349e-10
NZ_CP024595.1\|WP_021664633.1\|1090002_1091058_-\|glycosyltransferase-family-9-protein	gnl\|CDD\|340821	cd03789, GT9_LPS_heptosyltransferase, lipopolysaccharide heptosyltransferase and similar proteins. Lipopolysaccharide heptosyltransferase (2.4.99.B6) is involved in the biosynthesis of lipooligosaccharide (LOS). Lipopolysaccharide (LPS) is a major component of the outer membrane of gram-negative bacteria. LPS heptosyltransferase transfers heptose molecules from ADP-heptose to 3-deoxy-D-manno-octulosonic acid (KDO), a part of the inner core component of LPS. This family also contains lipopolysaccharide 1,2-N-acetylglucosaminetransferase EC 2.4.1.56 and belongs to the GT-B structural superfamily of glycoslytransferases, which have characteristic N- and C-terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility.	1.22899e-44
NZ_CP024595.1\|WP_010956235.1\|1087671_1088682_+\|cobalamin-biosynthesis-protein-CobD	gnl\|CDD\|377002	pfam03186, CobD_Cbib, CobD/Cbib protein. This family includes CobD proteins from a number of bacteria, in Salmonella this protein is called Cbib. Salmonella CobD is a different protein. This protein is involved in cobalamin biosynthesis and is probably an enzyme responsible for the conversion of adenosylcobyric acid to adenosylcobinamide or adenosylcobinamide phosphate.	1.48718e-121
NZ_CP024595.1\|WP_099779282.1\|1084598_1085165_+\|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase	gnl\|CDD\|376665	pfam01923, Cob_adeno_trans, Cobalamin adenosyltransferase. Cobalamin adenosyltransferase This family contains the gene products of PduO and EutT which are both cobalamin adenosyltransferases. PduO is a protein with ATP:cob(I)alamin adenosyltransferase activity. The main role of this protein is the conversion of inactive cobalamins to AdoCbl for 1,2-propanediol degradation.The EutT enzyme appears to be an adenosyl transferase, converting CNB12 to AdoB12.	1.56545e-77
NZ_CP024595.1\|WP_004584294.1\|1068048_1068522_+\|PaaI-family-thioesterase	gnl\|CDD\|239527	cd03443, PaaI_thioesterase, PaaI_thioesterase is a tetrameric acyl-CoA thioesterase with a hot dog fold and one of several proteins responsible for phenylacetic acid (PA) degradation in bacteria. Although orthologs of PaaI exist in archaea and eukaryotes, their function has not been determined. Sequence similarity between PaaI, E. coli medium chain acyl-CoA thioesterase II, and human thioesterase III suggests they all belong to the same thioesterase superfamily. The conserved fold present in these thioesterases is referred to as an asymmetric hot dog fold, similar to those of 4-hydroxybenzoyl-CoA thioesterase (4HBT) and the beta-hydroxydecanoyl-ACP dehydratases (FabA/FabZ).	4.83078e-11
NZ_CP024595.1\|WP_004584296.1\|1069222_1070590_-\|lactate-utilization-protein	gnl\|CDD\|224062	COG1139, COG1139, Uncharacterized conserved protein containing a ferredoxin-like domain [Energy production and conversion].	9.77623e-138
NZ_CP024595.1\|WP_099779281.1\|1083256_1084576_+\|cobyrinate-a,c-diamide-synthase	gnl\|CDD\|234896	PRK01077, PRK01077, cobyrinate a,c-diamide synthase.	0
NZ_CP024595.1\|WP_004584297.1\|1070586_1071408_-\|(Fe-S)-binding-protein	gnl\|CDD\|223325	COG0247, GlpC, Fe-S oxidoreductase [Energy production and conversion].	1.60129e-46
NZ_CP024595.1\|WP_023846767.1\|1078992_1082400_+\|hypothetical-protein	gnl\|CDD\|380475	cd20477, Cas13b_Pb-like, Class 2 type VI-B CRISPR-associated RNA-guided ribonuclease Cas13b from Prevotella buccae and similar Cas13b proteins. CRISPR-Cas (clustered regularly interspaced short palindromic repeats and CRISPR-associated proteins) adaptive immune systems defend microbes against foreign nucleic acids via RNA-guided endonucleases. These systems are divided into two classes: class 1 systems utilize multiple Cas proteins and CRISPR RNA (crRNA) to form an effector complex while class 2 systems employ a large, single effector with crRNA to mediate interference. Class 2 type VI CRISPR-Cas13 systems use a single enzyme to target RNA using a programmable crRNA guide and are divided into four subtypes based on the identity of the Cas13 protein (Cas13a-d). The Cas13 proteins are capable of both pre-crRNA processing and target RNA cleavage, which protect the host from phage attacks. Once bound to a target RNA, their non-specific RNase activity is activated. Cas13b has many distinctive features compared to the other Cas13 proteins, including the lack of significant sequence similarity, disparate crRNA repeat region, and double-sided protospacer flanking sequence (PFS)-dependent target RNA cleavage.	0
NZ_CP024595.1\|WP_099779277.1\|1071647_1072520_-\|phosphoserine-phosphatase-SerB	gnl\|CDD\|319803	cd07500, HAD_PSP, phosphoserine phosphatase (PSP), similar to Methanococcus Jannaschii PSP and Saccharomyces cerevisiae SER2p. This family includes Methanococcus jannaschii PSP, and Saccharomyces cerevisiae phosphoserine phosphatase SER2p, EC 3.1.3.3, which participates in a pathway whereby serine and glycine are synthesized from the glycolytic intermediate 3-phosphoglycerate; phosphoserine phosphatase catalyzes the hydrolysis of phospho-L-serine to L-serine and inorganic phosphate, the third reaction in this pathway. This family belongs to the haloacid dehalogenase-like (HAD) hydrolases, a large superfamily of diverse enzymes that catalyze carbon or phosphoryl group transfer reactions on a range of substrates, using an active site aspartate in nucleophilic catalysis. Members of this superfamily include 2-L-haloalkanoic acid dehalogenase, azetidine hydrolase, phosphonoacetaldehyde hydrolase, phosphoserine phosphatase, phosphomannomutase, P-type ATPases and many others. HAD hydrolases are found in all three kingdoms of life, and most genomes are predicted to contain multiple HAD-like proteins. Members possess a highly conserved alpha/beta core domain, and many also possess a small cap domain, the fold and function of which is variable. HAD hydrolases are sometimes referred to as belonging to the DDDD superfamily of phosphohydrolases.	1.59265e-57
NZ_CP024595.1\|WP_004584374.1\|1091141_1091747_-\|DUF4254-domain-containing-protein	gnl\|CDD\|379447	pfam14063, DUF4254, Protein of unknown function (DUF4254). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and eukaryotes. Proteins in this family are typically between 195 and 207 amino acids in length.	8.54226e-84
NZ_CP024595.1\|WP_099779283.1\|1086650_1087658_+\|threonine-phosphate-decarboxylase	gnl\|CDD\|273466	TIGR01140, L_thr_O3P_dcar, L-threonine-O-3-phosphate decarboxylase. This family contains pyridoxal phosphate-binding class II aminotransferases (see pfamAM:pfam00222) closely related to, yet distinct from, histidinol-phosphate aminotransferase (HisC). It is found in cobalamin biosynthesis operons in Salmonella typhimurium and Bacillus halodurans (each of which also has HisC) and has been shown to have L-threonine-O-3-phosphate decarboxylase activity in Salmonella. Although the gene symbol cobD was assigned in Salmonella, cobD in other contexts refers to a different cobalamin biosynthesis enzyme, modeled by pfam03186 and called cbiB in Salmonella. [Biosynthesis of cofactors, prosthetic groups, and carriers, Heme, porphyrin, and cobalamin].	4.04367e-116
NZ_CP024595.1\|WP_005873513.1\|1068632_1069217_-\|hypothetical-protein	gnl\|CDD\|224473	COG1556, COG1556, Uncharacterized conserved protein [Function unknown].	2.88283e-18
NZ_CP024595.1\|WP_054190948.1\|1085161_1086658_+\|cobyric-acid-synthase	gnl\|CDD\|234838	PRK00784, PRK00784, cobyric acid synthase.	0

>NZ_CP024595.1|WP_023846767.1|1078992_1082400_+|hypothetical-protein
MNTVPASENKGQSRTVEDDPQYFGLYLNLARENLIEVESHVRIKFGKKKLNEESLKQSLLCDHLLSVDRWTKVYGHSRRYLPFLHYFDPDSQIEKDHDSKTGVDPDSAQRLIRELYSLLDFLRNDFSHNRLDGTTFEHLEVSPDISSFITGTYSLACGRAQSRFADFFKPDDFVLAKNRKEQLISVADGKECLTVSGLAFFICLFLDREQASGMLSRIRGFKRTDENWARAVHETFCDLCIRHPHDRLESSNTKEALLLDMLNELNRCPRILYDMLPEEERAQFLPALDENSMNNLSENSLNEESRLLWDGSSDWAEALTKRIRHQDRFPYLMLRFIEEMDLLKGIRFRVDLGEIELDSYSKKVGRNGEYDRTITDHALAFGKLSDFQNEEEVSRMISGEASYPVRFSLFAPRYAIYDNKIGYCHTSDPVYPKSKTGEKRALSNPRSMGFISVHDLRKLLLMELLCEGSFSRMQSDFLRKANRILDETAEGKLQFSALFPEMRHRFIPPQNPKSKDRREKAETTLEKYKQEIKGRKDKLNSQLLSAFDMNQRQLPSRLLDEWMNIRPASHSVKLRTYVKQLNEDCRLRLRKFRKDGDGKARAIPLVGEMATFLSQDIVRMIISEETKKLITSAYYNEMQRSLAQYAGEENRRQFRAIVAELHLLDPSSGHPFLSATMETAHRYTEDFYKCYLEKKREWLAKTFYRPEQDENTKRRISVFFVPDGEARKLLPLLIRRRMKEQNDLQDWIRNKQAHPIDLPSHLFDSKIMELLKVKDGKKKWNEAFKDWWSTKYPDGMQPFYGLRRELNIHGKSVSYIPSDGKKFADCYTHLMEKTVQDKKRELRTAGKPVPPDLAADIKRSFHRAVNEREFMLRLVQEDDRLMLMAINKMMTDREEDILPGLKNIDSILDEENQFSLAVHAKVLEKEGEGGDNSLSLVPATIEIKSKRKDWSKYIRYRYDRRVPGLMSHFPEHKATLDEVKTLLGEYDRCRIKIFDWAFALEGAIMSDRDLKPYLHESSSREGKSGEHSTLVKMLVEKKGCLTPDESQYLILIRNKAAHNQFPCAAEMPLIYRDVSAKVGSIEGSSAKDLPEGSSLVDSLWKKYEMIIRKILPILDPENRFFGKLLNNMSQPINDL
>NZ_CP024595.1|WP_005873518.1|1078279_1078996_+|hypothetical-protein
MEKFSLYDFLAIILPGIAFIVVFRIIFSSLHLSLPVDIPLGLESTIVYALICGAVLYVLSFSLVKLFPRLFGLYRHVADLYQKMKALHPIMNDTLNRQAERWGLGKIYLSEEEFCQSEEKEKIRMLQSDFYDRMWYRLDFRGKLGSAKSFQCYYFFFRHSFWGLVLISLILLSYKLLAYIPACDMEDIGWREYSDIAVPIMILSALFVFLAQWFRIKMVEKMYWTFYISLIEQENSNL
>NZ_CP024595.1|WP_157766763.1|1076508_1077093_-|hypothetical-protein
MTSREIEEFDQKLSDYTMARYMRLLYFLCLADAKQRGETGTNSGGKLLSIFDNFVAYQRGPVEEDIYFRRYDEGVFTHFIFDEEGRLKLRQKSDSSPLPEMVEEADQKAVAKALEELGRLRIGDTHRGKSILEQTDMVLVDLSHSLSQEVWPAAYFYSEQDGRISKILEDAEILQKEITAFMSKCITTRHRNHE
>NZ_CP024595.1|WP_099779279.1|1075509_1076271_-|hypothetical-protein
MTKGLRTEIEHIIIKYPKDLNIMCRLRKTAVFEFFVSKLIGLDLAKIKEMTSGEIEEFNKKLSDYSMTRYMKLLYFLCLVDAGEEKEGGEEKEGGEGETKSGEKLLSIFDNFVAYRNGPIEDDIYLNRENEGEFTHFIFEEGCLKLRQKSDLSLLPEMVENADQKAVDKALEELEKCQIGKTCQEKSVLQQTDTVLVDLSHELNVWPAAYYYSKEGGKMSTILLGQDGVRQKEVEAFYGKTTKHPAAMQPTLQ
>NZ_CP024595.1|WP_099779278.1|1072739_1075412_-|hypothetical-protein
MESNSNIDEFISIVKDICLLYQSAVYQELIKDLSTDLNSLLTKKLEYILNNNPTSPFFDNFNKSLLKGIERSREASEGMNNESYIETEVNEILSAQERILTEEDHKATIRKLRSEITDCIQKFQDKKRDLIKAVISRDVEKYNNILEEVGLDKKGLDKKITSRESLDRRCDTLDKMAQSLVLHFSCSLLQAEFLEDGEYSTKLNDITKEISQWYKDHEPEEAQFLPPILHRIFTLCQELSYTCQLIRTQIDTLPPETDEKNIRKHRVFHAPAYILKSEQYAGGVDAIEMLQANNFYDFAKMLITLTRVDISGVINHSTVSSLLLLYKLCSRLIGEKNNNDAQRRPSRSFFPWNGNIEKVFTLIQAKTSLLLVHSFYKPSIDESTGKLDLEKSISIPYSRVENFELLYEGEKYILKGKATPDLSLLCNTGFKEFDNLKPVTLSKINEKKLSDVGKSDIENYNTYIENGRAIRKNLPNQEELKKELIEGKEEFDSQYYPIDVLLSLMRTLEKEYTKKEDELGLDRTKYAEAMGILLKCFSENVQHYKEFVSADQKRALYENSFFTIDNHDDLSIFISSYGCKLFDTDALEHEVYPQYNRLYRKWLSKAQAEAKELTKEAADKASKASQKATIAAEVAQKASNKAAEAAQKASNEAAEAANQASNEAKSTIKEESNQILLHVRRESMSIISVFVALITFISVGISILKGVNNLPDYMILAGTLYVFIASIIGFLYFKKTETPQPTGETPQSKGETPQPTGETPQSKGETPQPTGETPQSKGETPQSTEKQFATRCKHFLKKIVSAKGILFSSIGFAVIMIVIGFSWKNDQKLNPKDVEIQEPFFKQIISTDQHVDPIIDQTSNSQKVQQYSLYADSTHKAPRTEASIPKKTSK
>NZ_CP024595.1|WP_099779277.1|1071647_1072520_-|phosphoserine-phosphatase-SerB
MNGDYRVYIMAARADLLHVAAVCRAVEAIGARIVQFVREADTYDPCVRLSVAYKGAKSLLIKALMPMARTYPIMLGIRREDTPVGRIGLVAFDLDSTLVRTEIMNELATAHGCLDEMGELTEAAMSGREEFPDNFSRRVSMLRGLPLAKLEELSASLPIVEGLSSLMRKFKEQGIRSAIISGGFRLYSHNIKERYGFDYICTSEAEVENGLLTGRLSGTIVDAKVKAEFLRSLAKELSLTPAEIIAVGDGANDVPMLDFSAGSIIFNSSAHPPSMPQLRIEAILQFMGCR
>NZ_CP024595.1|WP_004584297.1|1070586_1071408_-|(Fe-S)-binding-protein
MAEEEAFVPLQGIGTKVFKNTIIRFITMKVGLFIPCYVNAVYPEVGIATYKLLKSLDIDVDYPMDQTCCGQPMANAGFEQKAQKLALRFEELFESYDVVVGPSASCVAFVKENYDHILRPTGHVCKSAAKVRDICEFLHDDLKITSLPSRFAHKVSLHNSCHGVRELHLSTPSEVHRPYHNKVRRLLEMVQGIEVFEPKRIDECCGFGGMYSVEEPEVSTCMGHDKVLDHISTGAEYITGPDSSCLMHMQGVIDREKLPIKTIHAVEILAANL
>NZ_CP024595.1|WP_004584296.1|1069222_1070590_-|lactate-utilization-protein
MSTKHSEAAARFLENKAGAKWHDETLWMVRHKRDIQRDTVPEWEDLRQLAHDIKRYNVTHLDELLLRFEENARRNGVIVHWAKDAKEHNEILYGILRDHGVKKFVKSKSMLTEECHLNEYLIEKGINVIETDLGERILQLMEEPPSHIVMPAIHIKREAVSDLFHDKLGTEKGNYDPTYLTRAARKSLREDFISADAAMTGGNFAVASTGEVVVCTNEGNADMGMACQKLNICSFGLEKLVPDLDAVGVFTRLLARSGTGQPSTTYTAHYRKPHEGGELHYIIVDNGRTDIIENEEHVKTLNCIRCGACMNTCPVYRRSGGYSYTYFIPGPIGINLGMLKDPRRYSDNVSACSLCLSCSNVCPVKIDLGEQIYRWRQDLDHLGRASQEKKLMSAGMKYLMDSPWRFNTALKMAPMANSLPRFLLYNGLNAWGKGRELPRFASTSFNNWWKKNIKK
>NZ_CP024595.1|WP_005873513.1|1068632_1069217_-|hypothetical-protein
MDSRQIILDRIKQHTKQREPKPEMNFTPITYPDKVARFIEISRAVGGDAIELQPGQDINEVIRAAYPDAKRIGSALPYIHIATYKPDEVENPGDMNGTDLAIIEGEIGVCENGCVWVDQTIQKRAMFFISEYLVIVLDKTKLVHNMHEAYKRVAEIDSQSPYSCFISGPSKTADIEQSLVIGAHGARGAIVILK
>NZ_CP024595.1|WP_004584294.1|1068048_1068522_+|PaaI-family-thioesterase
MDKKSFQEYYATGFSHCYGCGTSNEHGLHVKSYWAEEHPDETVAYFRPDSHHTGGFPGFVYGGLIAAILDCHGNGTAAAAGYRFQSRPMDSEPNLRYVTANLNLNYRRPTPMGVDLELRAHIKEVTDRKVLMELSLIAEGQVTVEGSMLSVLLPEKK
>NZ_CP024595.1|WP_099779281.1|1083256_1084576_+|cobyrinate-a,c-diamide-synthase
MSVPIKRSHLLISAASSGGGKTTFTLGLLRLLRRRGLKVQPFKCGPDYIDPKYHRLACGTETVNLDAFMMSREHIARLYDRYGCEADVSIVEGVMGLFDGYDRMTGSSALLAENLRIPVLLLIHAGSTAYSVAPILYGFKHFRPGVAPVGVVFNKVGSASHYRYLEEAAADAGVASLGYLPKMKDLEVPSRHLGLSVEDLARYEYLPDRVADAIEKYVDVERLLGLMASDVDPVIEEESFTESSLHGRKCIAVADDEAFNFTYRENIRRLESRGRVVRFSPLRDNRLPDDCDFLYLPGGYPEFYLPALSANTSMKQSVRDYIESGGYALAECGGMMYLCDTIRGMDGRDYPMCGVLPETATMEGMRLHLGYRRMEYKGKELRGHEFHYSSTIGSMPSVAQQYNVRGEAVETPLYRYKNLLAGYTHLYWGEHDDLWMWFD
>NZ_CP024595.1|WP_099779282.1|1084598_1085165_+|cob(I)yrinic-acid-a,c-diamide-adenosyltransferase
MIYTKTGDKGTTGIFGGERVKKDDVRVEAYGTMDELNAAIGMIRTFLPEEDERQTVLYDIQMRMMAAMSIVATPAGKREQNPNHFPEEAAADCEAFIDRLLAETTDNGYFILPGGTPLSAHLQLARTIARRAERRLWTLHRSDEVPDAILKWMNRLSDLFFVMARHEMQQQGWSEEKWHRFAYKRKKK
>NZ_CP024595.1|WP_054190948.1|1085161_1086658_+|cobyric-acid-synthase
MTEGGKLRPIMFVGTGSDVGKSIIATGFCRIFRQDGYHPAPFKAQNMALNSFVTPEGLEIGRAQAVQAEAAGIPCHTDMNPVLLKPSSDHTSQVVLNGRPIGNRDAYEYFRREGRDELRTEVYAAFDRLASRFSPVVMEGAGSISELNLRDTDIVNMPMAIHAGACVILVADIDRGGVFASVYGSIMLLSAEERKYVRGIMINKFRGDLRLFDEGKKILEELCGIPVVGVIPYYKDIHIEEEDSVALSVKQYAAGQGRVNVAVVLLRYLSNYTDFNVLERDPRVHLYYTNNTEELRKADIIILPGSKSTLADLYELRRNGAAQAIVQAHRDGTTVLGICGGFQLMGMEVCDPDHIEGDIERLPGLGLLPVTTVMTGEKVTRRTAFRFLDHTDECEGYEIHMGRTMPVEGAASSPLNRLSDGTEDGYFVDATCMGTYVHGILDNPVVIDYLLSPYADKMEERKSFDYVRYKDEQYDKLADHLRRYADVPLIYQLMKDDD
>NZ_CP024595.1|WP_099779283.1|1086650_1087658_+|threonine-phosphate-decarboxylase
MIKGHGDDLYRHGPIRANFSSNIYNATERQGLLDHLHKRLDSIGSYPEPEPYSLEKGLADYHGIAADSISVTSGATEAIYLIAQAFRGSSSAVVVPTFSEYADACRLHGHRVDFISKPEEASSRYDMVWLCNPNNPTGRVWKTSELYRIVRECPSTIFIVDQSYEYFSTAEVLGTKEAISLPNLLLLHSLTKRFAIPGLRLGYLTAHASLTERIRVCRMPWSVNALAIAAGEYLVQQGFPTSIPLAELRVETERLRTAIGSMAGYEVEPTDTHFMLVRCRHHSAADLKAVLADQYGLLIRDASNFEGLDAHCIRIATQTREQNDWLIDALRSISF
>NZ_CP024595.1|WP_010956235.1|1087671_1088682_+|cobalamin-biosynthesis-protein-CobD
MQGSVLILLLFLLPLLLGWLADYFLGDPLSLPHPIVGFGRMIAFGEKRLNKGNYRKVKGAFMSVFYIVAVFLLTLLILLGLVFVCVYTILLDDFFRIAVAFAVASLILAIGIFFCLAGTTLIREVRMVFEAVDRSLEEGRKQVTRIVGRDTAALSAQEVRTAALETLSENLSDGVVAPMFWYMWLGLPGMMAYKMINTLDSMIGYKTARYFLFGRIAAKIDDVANYIPARLTAWLMILVSGKLHLFSFVRRYGRQHASPNSGYPEAALAGILNCRFGGTHDYFGESISKPYIGHNERELATADMQIAIRINRRVELVMLLLTFVVSWITSSLFLFA
>NZ_CP024595.1|WP_012458144.1|1089566_1090019_-|hypothetical-protein
MKLRINKLISDAGLGSRREAEKYITEGRVKINGRIARLTDLVCEKDIVLLDDIDIPIKDLIREEISLRKYEERLAPSASNQGRQDEKRKNPRPKQHKEVPSQRNAGKPRSESRIRNRWEEGDEDDFDFDRGRGFRKGNRKNDSSVKKFRH
>NZ_CP024595.1|WP_021664633.1|1090002_1091058_-|glycosyltransferase-family-9-protein
MARYLIVRLSAIGDVAMTIPVLYAVAKAYPQHSFTLLTQPFLTSLLINPPNNLEGMGIDIKHEESSLVGLLTYIGRLKDEQFDYVIDLHNVIRSKIIRFYLRFFGVKGFSLKKPRLQLRQLTAKPPKKPTRLPSVIERYAQVFHKAGLEIHPPYPILLNDSGHISTELPIVEIGSGHHLIGIAPFAGHEAKTYPPEKMHEVVRTLAERDDVQIFLFGGKGKEKNILEQWADESPRIVSVAGLLSLPEELSLIHALRCMISMDSANMHFASLVGTRVISIWCATHPAAGFLGYGQRIEDCIGADLDCRPCSVFGNKPCFRKDYACRTQIEPQLIINKIVSTLTDLNSDETEN
>NZ_CP024595.1|WP_004584374.1|1091141_1091747_-|DUF4254-domain-containing-protein
MTISKLCNRIFAEAIQAYNVTDSVDAPCNNPYRPQTIEHYLFLKNWIDNAQWHLEDIIRDPNIDPADALVIKRRIDKSNQDRTDLVELIDSYFLDTYKDVKVLPDATINTESPAWAIDRLSILKLKIHNMRLATERPDADDAHRAKCQEKLRVLIEQDADLCTAIDQLVDDIAAGRKYMKVYKQMKMYNDPTLNPILLGKK
>NZ_CP024595.1|WP_058018901.1|1091906_1092323_-|hypothetical-protein
MRKIVVTALMGIGLLVGTTVNAQTQKKVETAKTEQTVKKQECTHQHDKACDAKKAGESCKDKAKDAKDCCKDKAKDANAKDCSKDKSKDCKKSDCHKSEKGECKSKHGHKSCEGKGKDKAEAGNCPHAKKHEKATDKQ
>NZ_CP024595.1|WP_099779284.1|1092461_1093610_-|iron-containing-alcohol-dehydrogenase
MNNFKFKNPTELIFGQGMIKELPKRVPAGVPVLVTFGSGSVRYNGVYRAVKDALEGYDLVEFWGIESNPKIETLRKAIAMGKEHNCQFVLAVGGGSVIDGSKLIAAAIPYEGDAWELVLKGYSRDTILPLRTVLTIPATGSEMNSGAIISREETKEKLVFRGNFPVFSILDPEVTFSLPPYQIACGLADSFVHVIEQYITTPGQSRLMDRWAESIMLTLKEIAPLIRENPHSYDLMADFMLCATMALNGFIAMGVTQDWATHMIGHEITALTGLTHGHTLAIVLPGTLRTLGHDHKREKMLQYAERIWDIKEGTEEERIDAAIARTEEFFRELGLKTRLEEMHIGSDVIKEIERRFIERGVSYGEALDVDGPMARRILEACR

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Crispr_ID: NZ_CP024595_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024595_4

2098289-2098436

Orphan

Consensus_repeat	Method
CTTAGCTCAGTCGGTTAGAGCATCTGACTGTTAATCAGAGGGTCCTTGGTTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP024595_4

>merge|NZ_CP024595|4|2098289-2098436|CRISPRCasFinder
CTTAGCTCAGTCGGTTAGAGCATCTGACTGTTAATCAGAGGGTCCTTGGTTCGAGCCCAAGAGAAAGCGCTCTCACAAGCCGTTTTTCTATTCTTCCTTAGCTCAGTTGGTTAGAGCATCTGACTGTTAATCAGAGGGTCCTTGGTTC

>NZ_CP024595|4|4|2098289-2098436|CRISPRCasFinder
CTTAGCTCAGTCGGTTAGAGCATCTGACTGTTAATCAGAGGGTCCTTGGTTC	GAGCCCAAGAGAAAGCGCTCTCACAAGCCGTTTTTCTATTCTTC
CTTAGCTCAGTTGGTTAGAGCATCTGACTGTTAATCAGAGGGTCCTTGGTTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024595.1\|WP_099779567.1\|2101244_2101949_-\|NAD-dependent-deacylase	unknown	unknown	gnl\|CDD\|234777
NZ_CP024595.1\|WP_099779569.1\|2103049_2103622_-\|N-acetyltransferase	unknown	unknown	gnl\|CDD\|100048
NZ_CP024595.1\|WP_099779561.1\|2081089_2082766_+\|sulfate-permease	unknown	unknown	gnl\|CDD\|183265
NZ_CP024595.1\|WP_021664650.1\|2082762_2083764_+\|tRNA-dihydrouridine-synthase-DusB	unknown	unknown	gnl\|CDD\|239200
NZ_CP024595.1\|WP_023846701.1\|2100015_2101170_+\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|277331
NZ_CP024595.1\|WP_099779563.1\|2088136_2089486_-\|sigma-54-dependent-Fis-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP024595.1\|WP_004583413.1\|2090850_2091879_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|273466
NZ_CP024595.1\|WP_021664641.1\|2098583_2099963_+\|MATE-family-efflux-transporter	unknown	unknown	gnl\|CDD\|240548
NZ_CP024595.1\|WP_005874769.1\|2105729_2106386_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779564.1\|2091926_2094938_-\|serine-hydrolase	unknown	unknown	gnl\|CDD\|366376
NZ_CP024595.1\|WP_099779568.1\|2102028_2103048_+\|acyltransferase-family-protein	unknown	unknown	gnl\|CDD\|225813
NZ_CP024595.1\|WP_099779562.1\|2084538_2086719_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_157766776.1\|2097676_2098099_-\|DUF1661-domain-containing-protein	unknown	unknown	gnl\|CDD\|285160
NZ_CP024595.1\|WP_099779565.1\|2095077_2097657_-\|ATP-dependent-Clp-protease-ATP-binding-subunit	unknown	unknown	gnl\|CDD\|223616
NZ_CP024595.1\|WP_021664648.1\|2086788_2088126_-\|GHKL-domain-containing-protein	unknown	unknown	gnl\|CDD\|227333
NZ_CP024595.1\|WP_021661646.1\|2108973_2109603_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_054191515.1\|2090070_2090841_-\|2-phosphosulfolactate-phosphatase	unknown	unknown	gnl\|CDD\|377205
NZ_CP024595.1\|WP_099779571.1\|2106382_2108605_-\|TonB-dependent-receptor	unknown	unknown	gnl\|CDD\|238657
NZ_CP024595.1\|WP_005874754.1\|2108684_2108981_-\|transcriptional-regulator	unknown	unknown	gnl\|CDD\|316153
NZ_CP024595.1\|WP_099779570.1\|2103634_2105056_-\|chromosomal-replication-initiator-protein-DnaA	unknown	unknown	gnl\|CDD\|273037

Protein	Function_ID	Function_description	E-value
NZ_CP024595.1\|WP_099779567.1\|2101244_2101949_-\|NAD-dependent-deacylase	gnl\|CDD\|234777	PRK00481, PRK00481, NAD-dependent deacetylase; Provisional.	1.49224e-107
NZ_CP024595.1\|WP_099779569.1\|2103049_2103622_-\|N-acetyltransferase	gnl\|CDD\|100048	cd03358, LbH_WxcM_N_like, WcxM-like, Left-handed parallel beta-Helix (LbH) N-terminal domain: This group is composed of Xanthomonas campestris WcxM and proteins with similarity to the WcxM N-terminal domain. WcxM is thought to be bifunctional, catalyzing both the isomerization and transacetylation reactions of keto-hexoses. It contains an N-terminal LbH domain responsible for the transacetylation function and a C-terminal isomerase domain. The LbH domain contains imperfect tandem repeats of a hexapeptide repeat motif (X-[STAV]-X-[LIV]-[GAED]-X), typical of enzymes with acyltransferase activity.	2.94769e-63
NZ_CP024595.1\|WP_099779561.1\|2081089_2082766_+\|sulfate-permease	gnl\|CDD\|183265	PRK11660, PRK11660, putative transporter; Provisional.	9.69659e-162
NZ_CP024595.1\|WP_021664650.1\|2082762_2083764_+\|tRNA-dihydrouridine-synthase-DusB	gnl\|CDD\|239200	cd02801, DUS_like_FMN, Dihydrouridine synthase-like (DUS-like) FMN-binding domain. Members of this family catalyze the reduction of the 5,6-double bond of a uridine residue on tRNA. Dihydrouridine modification of tRNA is widely observed in prokaryotes and eukaryotes, and also in some archaea. Most dihydrouridines are found in the D loop of t-RNAs. The role of dihydrouridine in tRNA is currently unknown, but may increase conformational flexibility of the tRNA. It is likely that different family members have different substrate specificities, which may overlap. 1VHN, a putative flavin oxidoreductase, has high sequence similarity to DUS. The enzymatic mechanism of 1VHN is not known at the present.	3.57186e-109
NZ_CP024595.1\|WP_099779565.1\|2095077_2097657_-\|ATP-dependent-Clp-protease-ATP-binding-subunit	gnl\|CDD\|223616	COG0542, clpA, ATP-binding subunits of Clp protease and DnaK/DnaJ chaperones [Posttranslational modification, protein turnover, chaperones].	0
NZ_CP024595.1\|WP_099779563.1\|2088136_2089486_-\|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].	8.15406e-167
NZ_CP024595.1\|WP_004583413.1\|2090850_2091879_-\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|273466	TIGR01140, L_thr_O3P_dcar, L-threonine-O-3-phosphate decarboxylase. This family contains pyridoxal phosphate-binding class II aminotransferases (see pfamAM:pfam00222) closely related to, yet distinct from, histidinol-phosphate aminotransferase (HisC). It is found in cobalamin biosynthesis operons in Salmonella typhimurium and Bacillus halodurans (each of which also has HisC) and has been shown to have L-threonine-O-3-phosphate decarboxylase activity in Salmonella. Although the gene symbol cobD was assigned in Salmonella, cobD in other contexts refers to a different cobalamin biosynthesis enzyme, modeled by pfam03186 and called cbiB in Salmonella. [Biosynthesis of cofactors, prosthetic groups, and carriers, Heme, porphyrin, and cobalamin].	2.20574e-68
NZ_CP024595.1\|WP_021664641.1\|2098583_2099963_+\|MATE-family-efflux-transporter	gnl\|CDD\|240548	cd13143, MATE_MepA_like, Subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins similar to Streptococcus aureus MepA. 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. This subfamily includes Streptococcus aureus MepA and Vibrio vulnificus VmrA and functions most likely as a multidrug efflux pump.	3.31861e-131
NZ_CP024595.1\|WP_099779564.1\|2091926_2094938_-\|serine-hydrolase	gnl\|CDD\|366376	pfam00933, Glyco_hydro_3, Glycosyl hydrolase family 3 N terminal domain.	3.22463e-77
NZ_CP024595.1\|WP_099779568.1\|2102028_2103048_+\|acyltransferase-family-protein	gnl\|CDD\|225813	COG3274, COG3274, Predicted O-acyltransferase [General function prediction only].	4.11416e-18
NZ_CP024595.1\|WP_054191515.1\|2090070_2090841_-\|2-phosphosulfolactate-phosphatase	gnl\|CDD\|377205	pfam04029, 2-ph_phosp, 2-phosphosulpholactate phosphatase. Thought to catalyze 2-phosphosulpholactate = sulpholactate + phosphate. Probable magnesium cofactor. Involved in the second step of coenzyme M biosynthesis. Inhibited by vanadate in Methanococcus jannaschii. Also known as the ComB family.	2.42409e-79
NZ_CP024595.1\|WP_157766776.1\|2097676_2098099_-\|DUF1661-domain-containing-protein	gnl\|CDD\|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	5.87983e-06
NZ_CP024595.1\|WP_023846701.1\|2100015_2101170_+\|metallophosphoesterase	gnl\|CDD\|277331	cd07385, MPP_YkuE_C, Bacillus subtilis YkuE and related proteins, C-terminal metallophosphatase domain. YkuE is an uncharacterized Bacillus subtilis protein with a C-terminal metallophosphatase domain and an N-terminal twin-arginine (RR) motif. An RR-signal peptide derived from the Bacillus subtilis YkuE protein can direct Tat-dependent secretion of agarase in Streptomyces lividans. This is an indication that YkuE is transported by the Bacillus subtilis Tat (Twin-arginine translocation) pathway machinery. YkuE belongs to the metallophosphatase (MPP) superfamily. MPPs are functionally diverse, but all share a conserved domain with an active site consisting of two metal ions (usually manganese, iron, or zinc) coordinated with octahedral geometry by a cage of histidine, aspartate, and asparagine residues. The MPP superfamily includes: Mre11/SbcD-like exonucleases, Dbr1-like RNA lariat debranching enzymes, YfcE-like phosphodiesterases, purple acid phosphatases (PAPs), YbbF-like UDP-2,3-diacylglucosamine hydrolases, and acid sphingomyelinases (ASMases). The conserved domain is a double beta-sheet sandwich with a di-metal active site made up of residues located at the C-terminal side of the sheets. This domain is thought to allow for productive metal coordination.	2.24699e-50
NZ_CP024595.1\|WP_021664648.1\|2086788_2088126_-\|GHKL-domain-containing-protein	gnl\|CDD\|227333	COG5000, NtrY, Signal transduction histidine kinase involved in nitrogen fixation and metabolism regulation [Signal transduction mechanisms].	7.37569e-33
NZ_CP024595.1\|WP_099779571.1\|2106382_2108605_-\|TonB-dependent-receptor	gnl\|CDD\|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	4.25858e-19
NZ_CP024595.1\|WP_005874754.1\|2108684_2108981_-\|transcriptional-regulator	gnl\|CDD\|316153	pfam13601, HTH_34, Winged helix DNA-binding domain.	5.20509e-38
NZ_CP024595.1\|WP_099779570.1\|2103634_2105056_-\|chromosomal-replication-initiator-protein-DnaA	gnl\|CDD\|273037	TIGR00362, DnaA, chromosomal replication initiator protein DnaA. DnaA is involved in DNA biosynthesis; initiation of chromosome replication and can also be transcription regulator. The C-terminal of the family hits the pfam bacterial DnaA (bac_dnaA) domain family. For a review, see Kaguni (2006). [DNA metabolism, DNA replication, recombination, and repair].	0

>NZ_CP024595.1|WP_157766776.1|2097676_2098099_-|DUF1661-domain-containing-protein
MLRKTWRENFFVLVPQVFISRAKTKNFTRVFFRIYEPQSRHFRFENQVSNKPRTSISPLCNSKSVSAGSSGSKKLFSCYRSRTESLCRAIGTSPSRPVRDRGLSANRTFASVIMTDEEVLNTRQTVIVMLKGINPNRAAR
>NZ_CP024595.1|WP_099779565.1|2095077_2097657_-|ATP-dependent-Clp-protease-ATP-binding-subunit
MAYDFTQTFRNSLEYSYQEATRLGVVAVTQDMLVLGIIRDGDNGAIDIMRNYGINLYELKRLIELEAIAESLPASPEESPIFTPSAREAIDDATDICADMEDEAVSPVHLLLSILNSTQESLVQKIFMKQGIKYDTILSDYFGQRNPSEGKSPSEMEILDGYQDNDFDDEEDESSPPSGNSGTGGGSGDAPEQNTGGGDITTTTRSGGDTPALDTFGTDITAMAAAGKLDPVVGREQEIERVIQILSRRKKNNPVLIGEPGVGKSAIVEGLAERIVNRKVSRILFDKRIISLDLAQMVAGTKYRGQFEERLKAVLDELKKNPQIILFIDEIHTIVGAGSAAGSMDTANMLKPALARGQVQCIGATTLDEYRKNIEKDGALERRFQKVPIAPSTAEETLTILQNIKEKYEDYHGVRYTDEAIKAAVELTDRYVSDRFFPDKAIDAMDEAGASVHITNVVAPKEIEILEAELASVRENKLLAVKAQNYELAASFRDQERRTQQQIAEEKKKWEEQMSKHRETVDENVVAHVVALMTGVPAERLSTGEGERLRTMADDLKTKVVGQDTAIEKMVRAIQRNRLGLRNEKKPIGSFLFLGPTGVGKTYLAKKLAEYLFEDENAMIRVDMSEYMEKFSVSRLVGAPPGYVGYEEGGQLTERVRRKPYSVVLLDEIEKAHADVFNLLLQVMDEGQLTDSLGRRVNFKNTVIIITSNVGTRQLKDFGQGIGFRSEKDEEANKEHSRSVIQKALNKTFSPEFLNRLDDIILFDQLGKTEIRRMVDIELKAVLARIHRAGYDLVLTDEAKDVIATKGYDLQYGARPLKRTLQNEVEDRLTDLILSGQIEKGQTLTLSARDGEIIVQEQA
>NZ_CP024595.1|WP_099779564.1|2091926_2094938_-|serine-hydrolase
MKRFLFSAITILSLSVLYTATASARTNMGAMHAQQSKDYPFLLFGGVDSKDVKRWVDDRMKAMSTEEKVGQLLMPVVYPSLQEEKVKQAEQLVRTCHIGGILFQKGTLSEQYTMTRRLQEAAGTPLLIALDGEWGLHMRLKDAPRFPRNMGLGHQKDNQLLYNYGREVARQCRLMGIHINFAPVLDVNNNPKNPVIGTRSFGDNPRRVAERGIAYAQGLEDGGVMAVAKHFPGHGNTTEDSHKTLPTVFASREELENTELFPFKEFFRAGLSGVMTAHLNVPALEAKKNTPSSLSHAICTDLLRQEMGFKGLIFTDGLAMQGVQTAGSQPISVRAILAGNDILLGPVDPVKTFSEVLAAVEDRTISKELLDEKCRKILAFKYALIICKGVSKEVPAEEVVRQVNSREAERMSEDLWRASITILKNKKQFLPLSEENRIACVNLDGAASNTFTQELGLTSKDCYSYAKGSNSTRTQELLSKLKGYDAVIVTVRHTQPDWAGTFLHRLTEQNHTAIVFFTSPYVADRIPVAMDKARAIVVAYENVKEAARMAAYKIRDRVVVSSGGGIPVVQEEEDTDPTANMMPPTELSSGLIPMPAVDRIAKEALRQGAFPGCRILAVHRDKVVYDKSFGTLDGSARGGKVSSSTIYDLASVTKVVATTPAVMLLVQDGKLKLSDRLGTLLPRFARTDLKDITVQQLLLHEAGLRPSINFYESLIDSSSLDGKLLSPRRSSGWVRVDANMWGNPFFGFRSDLVSGQFRPDYPFRFSSNLYLSKEVKEIVLNTIASTPRNGVGRYKYSDLGFILLQQIVEKVSGKSLNVFVEERIFRPIGAGSLGYLPLDKYSVSRIAPAQNDKFLRKSIVRGTVDDEAAACLGGISGNAGVFGTAEDVARVLDMFIHEGTYKGHRIIDQKIFRQFITTHGKGNRRCLGFDKGRASMAESASGSTYGHTGFTGTCVWVDPENELIFVFLSNRTYPNRLNKTLMTASIRPRLHQAIYEALGIAEQ
>NZ_CP024595.1|WP_004583413.1|2090850_2091879_-|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MIFGHGDEGITPLSSEIVNFSTTVWTDGDKDHLEKHLVENLNCIRHYPEPDAGTLRQMLAKRNSVDNNAILVTNGPTAAFYQIAQAFRGSRSLIAIPSFAEYEDACRMYEHEVCFYPSNEDIGEADFSNMDFCWLCNPNNPDGRLLQRTEILRLLNDHPDTTFVLDQSYVSFTTEEVIRPADIKGRKNLVMVYSFSHAYGIPGLRIGYIVANKDFMKRVAAFSTPWAVNALAIEAAKFILIHPAQFTLPIRKWQRNTVDFITALNRLDGVEVHPSGTTFFLLRLKKGTAAELKKYMLEEYNMLIRDASNFRGLDESYVRITTQRPAQNQLFIKALETFLEKY
>NZ_CP024595.1|WP_054191515.1|2090070_2090841_-|2-phosphosulfolactate-phosphatase
MLQISLCPSPVLYPYYKTEQEEYTVVIVDIFRAGTTITTALMNGAVGIIPIATVEEAEIYAGNGFLVGGERGTKRLPFARFGNAPEEYTRQAVEGKQLVLSTTNGTRAVDIAAGALHVIIGAFINLEAVARYCIAKQKPVMVLASGWQNRMSTEDCLFAGALAATIVRLGEEVICEDGASVFQELWGNYNTHEKLTAYLNGRDHYERLRANKLERSVPYCTSLNLTEIVPELTFKISAASTDCPANRLFLPVTPPF
>NZ_CP024595.1|WP_099779563.1|2088136_2089486_-|sigma-54-dependent-Fis-family-transcriptional-regulator
MKKSGNIIVVDDNKHVLTALKLLLTGSFETVTLLPSPKTLLSTIVEVHADVLLLDMNFSTGINTGNEGLYWLDQVRSRFPDLPVVLFTAYADIRLAVEALKRGASDFVVKPWNNAELLESLRMAMNKAASTQVTATPKEDDSVFLGKSKAMREVLELADRIGDTAAHVLITGENGTGKGVLAEYIHARSPRSRQPMLTVDMGALSETLFESELFGHVKGAFTDAKSDRAGKFETASGGTIFMDEIGNLSLALQAKLLAVLQQKVVTRVGSNTPIPVDVRIISATNSDLPLSVAEGRFREDLLYRLNTIHIEMPPLRRRREDIAPMAVFFLHRYARQYGKEVPELTPEAEALLSDYPWPGNVRELQHCIEKAVILSRSSSLSAADLSLPKSVDAHPTATGVASTPQTLDEMEKTAIEQALARNGSNLSNVARELGISRQTLYNKMKRYGL
>NZ_CP024595.1|WP_021664648.1|2086788_2088126_-|GHKL-domain-containing-protein
MGRRKTGSFGLHLLFTIVMAVVGTWSAAAGHYAITVFAAGLVIFSALRLRLLYRRHLQDLSLLLNAIENGDYSVRFSEMGGNVSHRTFNRTLNRIKEILSRSRDEAIAGEQFLVHVLEQIPVGIMMVAPEGYVYSTNTVLLRLLGLPVITHLDQLRRVSPDMPRLFRSAATDSGIHIKLTTEREEQEVSLRFSSFRIKGKIYHIYTLSNIGKELDARETESWIRLIRVMTHEIMNSIAPITSICDTLLDNLQSSADEEMLSTGLDTIRSTGVGLLSFVQDYRKFTAVPPPEKEDIALHAFLSGILRLQEELLSSNDIKVDIEEIPVELTVPADRRQLTSVLINLVKNAAEAEYPADTEKRLLRIRVEERLDSLDEHRLLLHVENNGTPIPQEVFDNMFVPFYTTKTGGSGIGLSLSRYIIRLHGGNLLARRTADGFTSFVIELPL
>NZ_CP024595.1|WP_099779562.1|2084538_2086719_-|hypothetical-protein
MVGQSLPSVSKEIRELSNRTEQQTSLSDRKESEAFALETVRMISDRTPYLFRLAEGRSWEADVRGRSWASRVLPIVHRLKHGGIPWKQYLSSDSLCMEARLYGKYDSVTGAYRRGVVSFRSDIPQRNKVDDLTALALLGENVYAEEFDFGNRQIFPNPIRREAEAFYTYRLDSLYEKDGITYRRIAFRGLSGLNHGTVTIDATHGQLAILEMRVMMKGVITESYRVELGEVEPDFFLPIGLSVVIDRNRLWASLHNGYSASISYTGEQLDKTVLPVYMPTDSSRYRLPDELPVAPVWAVRSSFGREDSSTYWKNVVVGRDHTLHQHVPWHRALAWGHKYRIGERWRLGNEGLVWALFYYNYADHLWLGQSLTAIYDMAPGIRWEIKPGLYYVTKRRKAVWTLDSKLYYSPPQRGLLQLSAGHRSFDLYSTRERIDQLTDLMMELLNGQGPTTRYDDKFVRLTNSIDLLPKLNVETSVMLAERNPLPHGETWSLFGGSITDILNISNADPDLPRIVPHHRLLEVRAKMTFNPRPYYRYTADGFLIREGEGIRAPLLSLSYRGAFGMGRKSDARFHHLDLSIQQRLVFSPAASLFYQLNVGGYFDRSVIYPSEYFFLKGGNAFWRFGDSMEAAFQTLPPYTATADKHLILQTSYRASRLLVNFLPFVFLKTNDEALHFKARWDMVSRKPYLEMGYSESIGTLMQVGVFYGGYNFFYERGVAIRFTFNM
>NZ_CP024595.1|WP_021664650.1|2082762_2083764_+|tRNA-dihydrouridine-synthase-DusB
MKIGAIDLGVEPLLLAPMEDVTDVAFRIMCKQFGADLVFSEFLSADALIRQVAGTFRKMAIDESERPMAVQIYGRDVASMVEAARLCESAGPDLIDLNFGCPVKRVAGKGAGSGMLRNIPLMIEITREVVKAVKLPVTVKTRLGWDNDSKIIVDLAEQLQDCGIAALTIHGRTRAQMYTGTADWTLIGEVKNNPRMQIPIIGNGDVTTPQEARRAFDVYGVDAVMVGRASIGQPWIFEDMKHFLRTGETLSSRPFSYYMDILRRQTLNNIRKLDERRGILHTRRHIAASPIFKGIPNFKPMRVAMLRATTQEGLFALMDEVEKMIGSADSAAV
>NZ_CP024595.1|WP_099779561.1|2081089_2082766_+|sulfate-permease
MIGSYFRPKLLDVFSGYNRERFMADLMAGVIVGIVALPLAIAFGIASGVSPETGLITAIIGGFIVSLLGGSSVQIGGPTGAFIVIVYGIIHKYGIEGLTIATIIAGILLLVMGVLRLGTLIKFIPYPIVVGFTAGIALTIFSIQMNDLFGLGITDMPGDFLGKWGAYFTNFKSVNLWAFGMGLLSIVIIMLSPRFTKKIPGSLIAIILMTVAAYLLRLQGIGEFETIGDRFTISAQLPKPTGVTLSLETIRQLFPPAFTIALLGAIESLLSASVADGVIGEKHNSNTELIAQGAANIVVPFFGGIPVTGAIARTMTNINNGGRSPIAGIIHAFVLLLILLFLGPLTAYIPMACLAGVLIIVSYNMSGWRSVANIGRGPRSDSLVMLVTFLLTVILDLTVAIEIGLLLAILLFMKRVTENTRITVATGRLDLTQTGEIAHHDEVLDIPKGVEVYEIEGPFFFGIANRFEEIMNTLGDHPDVRIIRMRHVPFMDSTGMHNLENLIKMSRKEGVSIVLSGVRKDVHEELATAGIVELLGEENVCADIQAALRQAQAIAQGA
>NZ_CP024595.1|WP_021664641.1|2098583_2099963_+|MATE-family-efflux-transporter
MSSQQIQALESEKIPKLLFHYALPAVVGTAVNSLYNIVDRIFIGNGVSEYALSGLAITFPILIFLMAFGMLVGAGASVRVSILLGRKDIKEAEHTLANAIFLTFFTQALTIIPCYIFMEPLLRLFGASERTLPYAMEYLQYVVPANIFSALSFGYNAIMRASGYPRKAMITMIIGAMTNVVLDYIFIYPLGMGISGAAIATVISMIVCSVYVLSHFFRKDSIVRFHRSAFRLSLPVIGSITAIGVAPFAMHLTGSLVNIIMNRSFVSYGETADATDLAIGAFGIINGYAMLFFMIIIGVAQGMQPIVGFNYGAKNPGRVKSVYRYSCGVNLLVSFLGFALAMLMPRTIVSLFTNSEQMIELSASALRTALIGLSLVGFQVTTTQFFQSIGFSHKAIFLSLTRQIIFLIPCLLIIPRFMGLDGVWWSLPISDLASVVLSFVLITIQMKHFNQSKKTTFAE
>NZ_CP024595.1|WP_023846701.1|2100015_2101170_+|metallophosphoesterase
MKVFLEAFLLQYLLTLYIAYRGGQALPQKNLWRKGFHLLMSVVFTLYLIGFAGNRVLPDAVMSCIMSVTGFWFVMSIYAMFAMVIVEIARVVDKRFLHRFDRLSERVQARIRLGLFVLIGLSSALLVIHGLNIVRYPVVKHMDIRLDRPAIDGRQSMKVALLTDIHISETVTAGHIREMVERTLAERPDIVLIGGDMIDYHGRYARRDSITEYMRRLQDETPMGAYYVLGNHEYRADEVEKREWFRSIGHLVIDQVVTPGNAFYLIGRDDSTNVFRAPLHKLMPHVDTTKASILLDHQPHKLDSVAMTGVDLALYGHTHNGQIWPFTILTQLAFEKSWGYLRKGHTQFYVSSGVGAAGPAIRVFTESEIVILNVRFASENKPVH
>NZ_CP024595.1|WP_099779567.1|2101244_2101949_-|NAD-dependent-deacylase
MNKKRLVVLSGAGMSAESGISTFRDANGLWENYPVEDVASIDGFRRNPALVLKFYNARRRDYAGCKPNAGHIGLAEMEKEYDVRIITQNVDDLHERAGSTRVIHLHGELMKNRSVATDSVLYPVDPTNPDLHVGDLAPDGCQLRPFIVWFGEAVPMIEPAIEEVTQADIFVVIGTSLNVYPAAGLLNYAPRNCPIYLIDPKPVRSTSRQDIRYIHAPATEGVRMLRQELRDIDR
>NZ_CP024595.1|WP_099779568.1|2102028_2103048_+|acyltransferase-family-protein
MTTKGRNTTVDVLRVLAGLMVIGIHTSGEYVLEGVAEGANFIAGLCWEAVVQPAVPIFVIISGAFVLGRNETWGDFYRKRIPRLLVLLAFWLPFYWLWLWLKGDDIGSYLASFWQGRSFVHLWYVVMLLGLYAVVPLLNEIIRRCEADGEKAARKRLWTLSTILLLLGILSNTYDYILGYNRFFPFLWPDYLGYFLVGYTLKCHAPQRSLPALSLYGLSTISLFFASRYAFEHGEGLYFYRNLSPLIVLSAISLFAFFVSWGGCGGKLARIGKMQGDILGIYLVHIAVLNVVTKILVLTTPSLMQCAWLNIPIRVGLVFFVSWGVVRLMKRLPICRYLV
>NZ_CP024595.1|WP_099779569.1|2103049_2103622_-|N-acetyltransferase
MVHPTAIVEDGCVLGQGTRVWHFSHLMCGAEVGENCNIGQNVVIMPEVRLGRGCKVQNNVSLYSGVVCEDYVFLGPSCVFTNVINPRAFIERKSEYRPTHLHEGVSIGANATILCGITIGAYAMVGAGTVVIRDVPPYALVVGNPARRIGWVSRAGHRLSFDDKGMAVCPETGERYREVEETGTIESVSD
>NZ_CP024595.1|WP_099779570.1|2103634_2105056_-|chromosomal-replication-initiator-protein-DnaA
MNYHSTNVNEIWDACLRILQDIVDERAYRTWFLPIIPVSIEGDTLTLQVPSQFFCEFLEGNFVEQLRTVLGRVIGPNASLQYNALVDNSSPKYPGTVTLAGCADGGQAAEQFDVNLLHRHMPNAATHSEAQDFDTQLNSRLNFRNFYQSECNYVARSVAEAIAASPGNTPMNPFFIYGASGVGKTHLCHALGLRVREMHPRLKVLYVSSHLFEMQFTTAARMGTINDFIAFYQQVDVLIIDDIQWLIGKKKTQLAFFQVFNHLYMLGKQIVLTSDKPPVDLNGMEERLVTRMAGATCVKIERPDLKLRREILHQRTLQSGVRLDESVLNFIAENVCDNVRELEGTLVSLITNSVVVGKEIDLTFAKRIVRQAVRLEKKEVTIECIQQAVSRVFQVQIEQMKSKSRKQDIVQARQVVMFLSKKHTAQSLSAIGELMGGRNHATVLHGCRCVTNEMEMNASFRSSVERAEQLIAN
>NZ_CP024595.1|WP_005874769.1|2105729_2106386_-|hypothetical-protein
MKTFKRIALLLVAGFAGLCATSAQGTAYAEVMNRKVAALDSVPPTEYATLAADFSRIAAVEGSDWMAAYYTAYCRIIPAFGNPSEADRLCEEAESMLSKAESLGGDLSEIACLRSMAASARLLVNPQERWQTYGAESSRQLAVALEANPANPRAYFLQAQSLLYTPAQFGGGKDKALPFAEKSVSCYAAATVSPAYAPHWGEQQARQLLMLCKAETQE
>NZ_CP024595.1|WP_099779571.1|2106382_2108605_-|TonB-dependent-receptor
MKRLISRTLIWFLLILCIPISLAAQRQIAGTVTDTKGRPIVLANVYPINSFDGMATDSLGRFRFTTSSTFPIRLVVSHINYHSDTLTIRKGDPMENIRIRLRETDDYKLSEVVVSVSAFGVGGKQNKTVLNPMDVYTNPSGNGDLSMALRQTPGLQDVGDREGFFVRGGASWETAVTIEGIRVKRFFGKNRFDAPARSRFETGMFSGLSLSTGGYEATEGGALSGLLRLRLAGKSPSSVGIGISPLFVNGGGGHLSRSNRFYIEQNASVSDAAYIRLLLKPEYKLPGTNRSYAYNARTIWNPTPRDEVKGLFLFVHDLSSSALRIPSPATAYMLYAGRNTYGFGMAVWRHDFEGGKTTSTLSAGYSEDHNRLHRQLEIEPDIESTFRTVERDANIRLRFDSRIKAWRLSYGSDYTYSEAKSSVREDKSSALPTLREHLVAAYAEALFPLSNRISATAGLRSEYSGLTESAIILPRLSATYKLSPSSRITLDAGGYAAPGDYYLSHGIVPQKREHSQQYNLTYEWRPSRTQVLRLQAYDKEYSRLTTLAPDGTASNLGKGYARGLDFFWKASGLIRSFEHWFSYSYTDARRQYLFSPDQERPDFVAKHTLSTVLKYWCAPISSLFNVSMSWRSGMTYHDPNIASPAYLNASLPANFSMSASYNYPFKYKKAGGVLVFSVHNLFNSDPTYGYRFGDKPIGGVYPSVRISTPYRQFYMVGLFINFGIDRRQEIMNTDIKIKSR
>NZ_CP024595.1|WP_005874754.1|2108684_2108981_-|transcriptional-regulator
MLRPLDPLLMSELRLAIMSVLMSVEEADFLYLKEVTGATSGNISVQLDKLSTAGYIEIEKGYNGKRPRTTCRATDAGREAFSAHFEALKSYLPTDSTH
>NZ_CP024595.1|WP_021661646.1|2108973_2109603_-|hypothetical-protein
MEYEPLTDSKKMEEKQLTPQESVQMIEKMLEQTRKRLIRGAGIPSLIWGYVTFATSLLILFVYPHIGYRANYLWMLIPIVGGSLTIICNRKRQKEAHARTQIDRFIDTTWITIGLNVTALSILAYRFPLAILPLVLILIGIATAITGFSHKVTLLKYSSIFGILVGYMLLVVPMNGKLMVLIFGLTFFLMHCVPGHYLCYLERKILRDA

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Crispr_ID: NZ_CP024595_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024595_5

2271481-2282122

Unclear

Consensus_repeat	Method
ATTTCAATTGCACCATACAGGAATTAAAAC	PILER-CR
ATTTCAATTGCACCATACAGGAATTAAAAC	CRISPRCasFinder
NNNNNNATTTCAATTGCACCATACAGGAATTAAAAC	CRT
ATTTCAATTGCACCATACAGGAATTAAAAC	PILER-CR

161 spacers

cas2,cas1,cas4,cas7,cas8b6,cas3,cas5,cas6

The CRISPR arrays of NZ_CP024595_5

>merge|NZ_CP024595|5|2271481-2282122|PILER-CR,CRISPRCasFinder,CRT,PILER-CR
ATTTCAATTGCACCATACAGGAATTAAAACAATTTGGGAATTACGATGAAGAAAAGCATTTTTTCATTTCAATTGCACCATACAGGAATTAAAACAAAAAAATTAGAATCTTTTATTCGCTCGTATATCGAAAATTTCAATTGCACCATACAGGAATTAAAACGTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTAATTTCAATTGCACCATACAGGAATTAAAACTTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTATATTTCAATTGCACCATACAGGAATTAAAACAATCTTCTTTAGTAAAGAATCTAAAAAGATCTTCTAATTTCAATTGCACCATACAGGAATTAAAACTTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTATTTCAATTGCACCATACAGGAATTAAAACGAACAACGAGCTTTATTTGAGAAGTATATAAATACTTATTTCAATTGCACCATACAGGAATTAAAACAATACTATTATATTCTCGTTGTTCTGTATAGATAGAATTTCAATTGCACCATACAGGAATTAAAACTTCAAAATCGTGTTCAAACGGAACCTCTTTTATAGTATTTCAATTGCACCATACAGGAATTAAAACGTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTAATTTCAATTGCACCATACAGGAATTAAAACGTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTAGATTTCAATTGCACCATACAGGAATTAAAACTTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTATTTCAATTGCACCATACAGGAATTAAAACTTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTATTTCAATTGCACCATACAGGAATTAAAACCTTGCATCGATATGTTCCCTGTTTCTTGATGTTCAATTTCAATTGCACCATACAGGAATTAAAACTCTGTACTATTGCAATAGCATAACCATTGTGCTAAGAATTTCAATTGCACCATACAGGAATTAAAACTCTGCAACAACATCGATGTATTTTTGTAGACGTTAGATTTCAATTGCACCATACAGGAATTAAAACTCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGACATTTCAATTGCACCATACAGGAATTAAAACTCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGACATTTCAATTGCACCATACAGGAATTAAAACTACGGTATAGAGTCTCAAGTACGTTGACTTCGGGTATTTCAATTGCACCATACAGGAATTAAAACTTGTGCTAAGAGAAACTTAATGCTGTTATATTCTCATTTCAATTGCACCATACAGGAATTAAAACAAAAAAATTAGAATCTTTTATTCGTTCGTATATCGAAAAATTTCAATTGCACCATACAGGAATTAAAACCCTATCTTTTTCACTTGAGGTAGCATCAACAAACTTATTTCAATTGCACCATACAGGAATTAAAACATCAACCTCTTCATATCTACTGGATAGTTGAAGTTATTTCAATTGCACCATACAGGAATTAAAACTATAATTCTTTAGGAGATAGTCCAGGATCTACATCAATTTCAATTGCACCATACAGGAATTAAAACAAGGAGGATGAGGAGTTTTTGAATAACTACATCAAATTTCAATTGCACCATACAGGAATTAAAACAGTCAGGTTGGTATCCATATGCCTCTAAGAGGCTGGATTTCAATTGCACCATACAGGAATTAAAACATGAGAGCGGGTGATATGATTGTAAGACTCAGAAAAATTTCAATTGCACCATACAGGAATTAAAACGATGTGAAGTTCTCCAGCACACCTTCGAGAGTGGAAATTTCAATTGCACCATACAGGAATTAAAACTCACGATAACTTCACGCTCAGAAAGATTGACTGGTTATTTCAATTGCACCATACAGGAATTAAAACGAGGGCGCAGATAGGGCTTAGAACCCTATCTGCTTTATTTCAATTGCACCATACAGGAATTAAAACGACAGGATATGCTATAGTTGCAAATTGAGTATATTTGATTTCAATTGCACCATACAGGAATTAAAACGCTAGGATATATAGGACAATAATATTCACTGTCCTTATTTCAATTGCACCATACAGGAATTAAAACTTCAACATCTCATGAGAGAATGTATAAATAGGCTATTTCAATTGCACCATACAGGAATTAAAACCGTATTGTTCGCGTAGTTTGTTGTAATACTCAGCGATTTCAATTGCACCATACAGGAATTAAAACTATGCCTCTAAGAGGCTGGATACTTCGATGGGTACGATTTCAATTGCACCATACAGGAATTAAAACTCAACAAAGGCTTGTGAGTATATGGCATTTCTATACCCATTTCAATTGCACCATACAGGAATTAAAACCCACGTGTCCCATATGCCATAAAACGCGAACCTCGATTTCAATTGCACCATACAGGAATTAAAACAAAGCATAAGTTCTATAGATTCTAGTTTAATTTATAATTTCAATTGCACCATACAGGAATTAAAACTATCGTTTTGTAGGTTAAATAGCCTCTCTATTTCTTATTTCAATTGCACCATACAGGAATTAAAACTGAGGGAGGTAACAAACCCCTGGGTAATAGAAAATGATTTCAATTGCACCATACAGGAATTAAAACGGAAAGATTATAAACTTTCTAGATCCATATCTGCTGTATTTCAATTGCACCATACAGGAATTAAAACATGTAGTAATTAAATCTATTATAAATCATATTTCTTATTTCAATTGCACCATACAGGAATTAAAACACACTCCCTTATTAAAGACGTAGATCCGGCAGCTGCATTTCAATTGCACCATACAGGAATTAAAACATAGGTAATGTAGTTCTCAGCTCTCGAACGGGAAATTTCAATTGCACCATACAGGAATTAAAACGTCTTGTGTGTGGATCTGCTCCTGATAATCCATCTGATTTCAATTGCACCATACAGGAATTAAAACTACTGTTGTTTTGTTAAACTTTTATTTTATGTCTGAATTTCAATTGCACCATACAGGAATTAAAACTTCTTAAACTCAGATAAATCTACTTCTAAATTTAGTAATTTCAATTGCACCATACAGGAATTAAAACAAGGGATTATCAAAATAGCGATGTTTTACATCTAATTTCAATTGCACCATACAGGAATTAAAACAGGTTCACTAACTGGCGGAATAAGTGTGATTCCACCATTTCAATTGCACCATACAGGAATTAAAACTAAGAAATCTACAATACTTCCAACTTATTCAAGAAAAATTTCAATTGCACCATACAGGAATTAAAACTGATAGACATATGAAGAGCTTCAGACAGTGCAAAATTTCAATTGCACCATACAGGAATTAAAACTAAGACTCGATAACCTCTTTCACAGAGTTCTCAAAGATTTCAATTGCACCATACAGGAATTAAAACAGCATTCTGTAGGAGCGAAGTTTTGTTTGTTTGTGTAATTTCAATTGCACCATACAGGAATTAAAACAACTTGAACTTTCGGTTGAGCTAATACAAAGATTATTTCAATTGCACCATACAGGAATTAAAACCTATAATGGAGTTAATATCAATCTGATTAAGAGCAAAATTTCAATTGCACCATACAGGAATTAAAACAACTGCAAATCTGTAAAAGTCTTTTTGGAATTCTTATTTCAATTGCACCATACAGGAATTAAAACACAGACTGGATTAAGATGGATAAGGAAGGAAATTTAGATTTCAATTGCACCATACAGGAATTAAAACAACTTAAACGTAGATTATAAAACTCTACCGCTGTAAATTTCAATTGCACCATACAGGAATTAAAACAAAGCTCATCGGTATGCTGCAAGAAAAAGATACACTATTTCAATTGCACCATACAGGAATTAAAACATATAAAGACCCTCAAAGAGGAGGGATTTAATATAATTTCAATTGCACCATACAGGAATTAAAACGAGGCTATACAGGTAATTTCTGCCTATTCGGCTTACCATTTCAATTGCACCATACAGGAATTAAAACACGAAATGATCAAAAAGGAGTTTATCCACCGCACATTTCAATTGCACCATACAGGAATTAAAACTTTCTTTTGCTTCTTTCTGATTGCGAGCGAATACGATTTCAATTGCACCATACAGGAATTAAAACACACATCATCTGTATAGAGTTTATATGTGTCGTAAAATTTCAATTGCACCATACAGGAATTAAAACTTTATTACGTTATAGAAATCATCTTCATCTGCTAACATTTCAATTGCACCATACAGGAATTAAAACAATTTTGGTATTACAATAAAGAATCGATGTTTTTCGATTTCAATTGCACCATACAGGAATTAAAACAGTAACGCTGCTTCTATAAAAAGTTTTAGCCCTCAATATTTCAATTGCACCATACAGGAATTAAAACAAATTAGGAACCTATAAAGAAGAGGAATAGATATGAATTTCAATTGCACCATACAGGAATTAAAACTCTCCTCTACATCCTCAGGAGAAGGAGACCATGCTGATTTCAATTGCACCATACAGGAATTAAAACCAGCTTGGGAAGCTGAATATATCTCGACCTTTTTGATTTCAATTGCACCATACAGGAATTAAAACTGTTTTCATGGTGCGGGCTTTTGCCCTGAGTTCTTATTTCAATTGCACCATACAGGAATTAAAACTAGCAGATCGGTTCCTGAATCACATAGGGCTATAGATTTCAATTGCACCATACAGGAATTAAAACTATAATCAAGCATTTATGTCTTACTCTAAGAATTTCAATTTCAATTGCACCATACAGGAATTAAAACATATATCGACAACTCCGGGAATAATGGTGCAAACACATTTCAATTGCACCATACAGGAATTAAAACAAGCGCAGCTTGTCGGTGGAGCAGCTACGGACGTTGTATTTCAATTGCACCATACAGGAATTAAAACTCAATCTATTGAAGAGGGGAAGAGAAGCATGTCAATTTCAATTGCACCATACAGGAATTAAAACCACGGGGCTTGTGCTCATACTATCGAATGTATGAGGATTTCAATTGCACCATACAGGAATTAAAACTTTCAGCCCTCAAATTTGAGAGGGCTGATTATTTTTATTTCAATTGCACCATACAGGAATTAAAACGCATTGTAAGAGAGGATTCTTCCTTCATAAAACGTTATTTCAATTGCACCATACAGGAATTAAAACTTGAACCACCTAATTGGGAGAAAGAAGAATTTTATAATTTCAATTGCACCATACAGGAATTAAAACCTGATGAGGCATTTCTTTCCTCTGCTGCCTTTTTACAATTTCAATTGCACCATACAGGAATTAAAACGCAACGGCGAATATTAAACTCTTCATAATAGTTTTATTTCAATTGCACCATACAGGAATTAAAACTAGTTTGGAGCGGTATATAGAAAAGAATCGGATCGTATTTCAATTGCACCATACAGGAATTAAAACTCGTGATGACGGCGAATAATCTTAGTTTCATGTTATATTTCAATTGCACCATACAGGAATTAAAACCCATATTCCTTTTGCTTTTGGTTACGGCTGTGCTGATTTCAATTGCACCATACAGGAATTAAAACCGAATCGCGTATTGGATACTATCGACATTTACGCGCTATTTCAATTGCACCATACAGGAATTAAAACGCATGGGTAAAAGTTAATGGGCGCAGTTTTGCGCTCATTTCAATTGCACCATACAGGAATTAAAACTGCAGGGCGACAAGGGCGCCCGATCCCTCGGAGAGGTATTTCAATTGCACCATACAGGAATTAAAACTCTGCAGACCGAACACTTTCAAATTTGACAGGTCGATTTCAATTGCACCATACAGGAATTAAAACCGAGACCTCGACGTTATAGACGCGCGCCTTCGCGGCATTTCAATTGCACCATACAGGAATTAAAACTGTCGATGTAATATCTTCGGGGTTAATTTCTTCAATTTCAATTGCACCATACAGGAATTAAAACTCGCCGCGCAGGCTATCTCATATCGTCTCTTTTCCCATTTCAATTGCACCATACAGGAATTAAAACTAAGTAACGACTTAAATACATAATAATCTGAAATTTTATTTCAATTGCACCATACAGGAATTAAAACCTTGGATAGGGTTTGCCGCGACACTTTGACGCGCTATTTCAATTGCACCATACAGGAATTAAAACTAAGTAACGACTTAAATACATAATAATCTGAAATTTATTTCAATTGCACCATACAGGAATTAAAACACTGTCTACATAGTGTTTAAGATAATGCTCAAAAAGATTTCAATTGCACCATACAGGAATTAAAACAATTTTAACAGTCTTTAAGACTTACATTAAAGAAAATTTCAATTGCACCATACAGGAATTAAAACCCGGAATCGGCGCAAAGGACTACGCAGAAGGAAGCCAATTTCAATTGCACCATACAGGAATTAAAACTCGATTTGGCATGAGATGTCTTTTATTTCGACATCCATTTCAATTGCACCATACAGGAATTAAAACTAAGTAACGACTTAAATACATAATAATCTGAAATTTATTTCAATTGCACCATACAGGAATTAAAACTCATTAAAAATATCATCTGTATGTAGCTGCAGTACAATTTCAATTGCACCATACAGGAATTAAAACCTGAAAACTCAAATAGTTTGATGATTTATTGCATAATTTCAATTGCACCATACAGGAATTAAAACTCATTAAAAATATCATCTGTATGTAGCTGCAGTACATATTTCAATTGCACCATACAGGAATTAAAACGATTTTCTGGTACTTGATGATTATTATAGTAGCACAATTTCAATTGCACCATACAGGAATTAAAACAGATTCTTATTATAATTATTTCTTATCGTACTTAAAATTTCAATTGCACCATACAGGAATTAAAACTCATTAAAAATATCATCTGTATGTAGCTGCAGTACATATTTCAATTGCACCATACAGGAATTAAAACTAAGTAACGACTTAAATACATAATAATCTGAAATTTTATTTCAATTGCACCATACAGGAATTAAAACAGATTCTTATTATAATTATTTCTTATCGTACTTAAAATTTCAATTGCACCATACAGGAATTAAAACTCACGAACAAGACGCAGCTGATAAGCGCAATCAACTATTTCAATTGCACCATACAGGAATTAAAACACATAGCACGGTTTATCTACAGAGACAACTCCTCAAATTTCAATTGCACCATACAGGAATTAAAACAAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCCATTTCAATTGCACCATACAGGAATTAAAACTTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAATATTTCAATTGCACCATACAGGAATTAAAACAAAAAAGAAGAATAACCATGTTAGGAGCGATAATTGATTTCAATTGCACCATACAGGAATTAAAACTCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAAATTTCAATTGCACCATACAGGAATTAAAACAGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGCATTTCAATTGCACCATACAGGAATTAAAACTTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTGATTTCAATTGCACCATACAGGAATTAAAACACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGCATTTCAATTGCACCATACAGGAATTAAAACTATACTCTGTTACGTCCATCTTGTTAGATGAACAAGATTCCAATTGCACCATACAGGAATTAAAACAGAGAGAATCGTATATTTCAATCGATCCGCCACTGGATTTCAATTGCACCATACAGGAATTAAAACGAACCAAGACCTTATAAAGCTCTTCCACAAGGTTGATTTCAATTGCACCATACAGGAATTAAAACCGCTGTTTCTTTCTACTAAAGCTGTCGTTTTCATAAATTTCAATTGCACCATACAGGAATTAAAACACATAAAATATCGAACGCTAAAATTTAAAAACGAAGAATTTCAATTGCACCATACAGGAATTAAAACTGTACTCACGCTTTATGCCGGCTCCTCATACTCGGCATTTCAATTGCACCATACAGGAATTAAAACTCGATGATGAGAAGTGCTGCGAACCCTTCAACTGGATTTCAATTGCACCATACAGGAATTAAAACATCACGATATATATCGTCACCCTGAGAAGCCGGGAATTTCAATTGCACCATACAGGAATTAAAACTCACGAACAAGACGCAGCTGATAAGCGCAATCAACTATTTCAATTGCACCATACAGGAATTAAAACACATAGCACGGTTTATCTACAGAGACAACTCCTCAAATTTCAATTGCACCATACAGGAATTAAAACAAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCCATTTCAATTGCACCATACAGGAATTAAAACTTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAATATTTCAATTGCACCATACAGGAATTAAAACAAAAAAGAAGAATAACCATGTTAGGAGCGATAATTGATTTCAATTGCACCATACAGGAATTAAAACTCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAAATTTCAATTGCACCATACAGGAATTAAAACAGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGCATTTCAATTGCACCATACAGGAATTAAAACTTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTGATTTCAATTGCACCATACAGGAATTAAAACATACGTCGGCTTTTCGGTATATGGCCCTATCAATGATTTCAATTGCACCATACAGGAATTAAAACATATTGAAAATAGAAAGAACGAAAAAGAAATCGAAAATTTCAATTGCACCATACAGGAATTAAAACACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGCATTTCAATTGCACCATACAGGAATTAAAACTATACTCTGTTACGTCCATCTTGTTAGATGAACAAGATTCCAATTGCACCATACAGGAATTAAAACAGAGAGAATCGTATATTTCAATCGATCCGCCACTGGATTTCAATTGCACCATACAGGAATTAAAACCTTTGCGTATCAGGATCGTGCGACTCTTGTAGCTGAATTTCAATTGCACCATACAGGAATTAAAACTGCTTGAATAACTACATTAGCATCAATAGGAACGTATTTCAATTGCACCATACAGGAATTAAAACTAAAGTATTCTCCTCGATAGTAGAAATAATGCTAATTTCAATTGCACCATACAGGAATTAAAACATGTTGGGTCTATAGAATCTCCGTCCTCCAAAGGGGATTTCAATTGCACCATACAGGAATTAAAACGGTGAAAATATACTCCAGACTAGGTTAGAAAGGAAATTTCAATTGCACCATACAGGAATTAAAACACAGCTACTGCGATAGTAGAAATAATGCTAACTAATTTCAATTGCACCATACAGGAATTAAAACCAGTTTATGTTATTGGCTTAGAGCGTAAAAGGTTTAATTTCAATTGCACCATACAGGAATTAAAACCGATCGATCAGTCGATTACAGCAGCTCAAAGCCTCGATTTCAATTGCACCATACAGGAATTAAAACGCATCGCGACCATCGATGACGAACGCCGCCTTCGTAATTTCAATTGCACCATACAGGAATTAAAACTCTATACATGTGTATAGAATCTTCTTGCCATTAAACATTTCAATTGCACCATACAGGAATTAAAACTGAACACATCACTCTGCATGATCTGAGCATGGTAGTATTTCAATTGCACCATACAGGAATTAAAACTGGGGAGGATACACGGATACGGCAGGTGAAATCGTCATTTCAATTGCACCATACAGGAATTAAAACAGAATAATCAATGGAAGAATTAGAATGGATTTTTCATTTCAATTGCACCATACAGGAATTAAAACGTTCTCGTTCTTTCTGAGCTTGATGTAGGGATCGGCATTTCAATTGCACCATACAGGAATTAAAACCGCCTGCGGCCTTATTTTCGTCGGCGTTGTGCTATATTTCAATTGCACCATACAGGAATTAAAACCAGCTCGGCACACTCTTTGTAGCCGAACACTCGCCGATTTCAATTGCACCATACAGGAATTAAAACGCGTTTCTGAAGAATACGCTTTTTCATATTGCTCTCATTTCAATTGCACCATACAGGAATTAAAACCCTCGCGGCAAGGGCAAATCCACCGATCCCGCCGAATTTCAATTGCACCATACAGGAATTAAAACTGAATTCTTTTGAGACTATTAAAACAGGAGCTCTTAATTTCAATTGCACCATACAGGAATTAAAACACGAGCCTATTGCAGAGCTTACAGTCGAACTGCGGCATTTCAATTGCACCATACAGGAATTAAAACAGACGGAGGTAAAGGGCTTTCAGGAGCAAGGCGAAAATTTCAATTGCACCATACAGGAATTAAAACATCTCAGCCCGTCTATCAAGTGGGTGGGCACAAGTCATTTCAATTGCACCATACAGGAATTAAAATGTCGGTCGAGACTACGAGGACTTCCGGCTCAGGGAAATTTCAATTGCACCATACAGGAATTAAAAT

>NZ_CP024595|5|3|2271481-2272963|PILER-CR
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTGGGAATTACGATGAAGAAAAGCATTTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGCTCGTATATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATCTTCTTTAGTAAAGAATCTAAAAAGATCTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACAACGAGCTTTATTTGAGAAGTATATAAATACTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATACTATTATATTCTCGTTGTTCTGTATAGATAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAAACGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGCATCGATATGTTCCCTGTTTCTTGATGTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGTACTATTGCAATAGCATAACCATTGTGCTAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAACAACATCGATGTATTTTTGTAGACGTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TACGGTATAGAGTCTCAAGTACGTTGACTTCGGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGTGCTAAGAGAAACTTAATGCTGTTATATTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGTTCGTATATCGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTATCTTTTTCACTTGAGGTAGCATCAACAAACTT
ATTTCAATTGCACCATACAGGAATTAAAACATCAACCTCTTCATATCTACTGGATAGTTGAAGTTATTTCAATTGCACCATACAGGAATTAAAACTATAATTCTTTAGGAGATAGTCCAGGATCTACATCAATTTCAATTGCACCATACAGGAATTAAAAC	AAGGAGGATGAGGAGTTTTTGAATAACTACATCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTCAGGTTGGTATCCATATGCCTCTAAGAGGCTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGAGAGCGGGTGATATGATTGTAAGACTCAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GATGTGAAGTTCTCCAGCACACCTTCGAGAGTGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGATAACTTCACGCTCAGAAAGATTGACTGGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGGCGCAGATAGGGCTTAGAACCCTATCTGCTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GACAGGATATGCTATAGTTGCAAATTGAGTATATTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCTAGGATATATAGGACAATAATATTCACTGTCCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAACATCTCATGAGAGAATGTATAAATAGGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	CGTATTGTTCGCGTAGTTTGTTGTAATACTCAGCG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATGCCTCTAAGAGGCTGGATACTTCGATGGGTACG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAACAAAGGCTTGTGAGTATATGGCATTTCTATACCC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCACGTGTCCCATATGCCATAAAACGCGAACCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCATAAGTTCTATAGATTCTAGTTTAATTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TATCGTTTTGTAGGTTAAATAGCCTCTCTATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAGGGAGGTAACAAACCCCTGGGTAATAGAAAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGAAAGATTATAAACTTTCTAGATCCATATCTGCTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTAGTAATTAAATCTATTATAAATCATATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACTCCCTTATTAAAGACGTAGATCCGGCAGCTGC
ATTTCAATTGCACCATACAGGAATTAAAAC	ATAGGTAATGTAGTTCTCAGCTCTCGAACGGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTCTTGTGTGTGGATCTGCTCCTGATAATCCATCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TACTGTTGTTTTGTTAAACTTTTATTTTATGTCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCTTAAACTCAGATAAATCTACTTCTAAATTTAGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGGGATTATCAAAATAGCGATGTTTTACATCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGGTTCACTAACTGGCGGAATAAGTGTGATTCCACC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGAAATCTACAATACTTCCAACTTATTCAAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGATAGACATATGAAGAGCTTCAGACAGTGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGACTCGATAACCTCTTTCACAGAGTTCTCAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGCATTCTGTAGGAGCGAAGTTTTGTTTGTTTGTGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTGAACTTTCGGTTGAGCTAATACAAAGATT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTATAATGGAGTTAATATCAATCTGATTAAGAGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTGCAAATCTGTAAAAGTCTTTTTGGAATTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGACTGGATTAAGATGGATAAGGAAGGAAATTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTAAACGTAGATTATAAAACTCTACCGCTGTAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCTCATCGGTATGCTGCAAGAAAAAGATACACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATAAAGACCCTCAAAGAGGAGGGATTTAATATA
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGCTATACAGGTAATTTCTGCCTATTCGGCTTACC
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAAATGATCAAAAAGGAGTTTATCCACCGCAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCTTTTGCTTCTTTCTGATTGCGAGCGAATACG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACATCATCTGTATAGAGTTTATATGTGTCGTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTATTACGTTATAGAAATCATCTTCATCTGCTAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTGGTATTACAATAAAGAATCGATGTTTTTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTAACGCTGCTTCTATAAAAAGTTTTAGCCCTCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAATTAGGAACCTATAAAGAAGAGGAATAGATATGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTCCTCTACATCCTCAGGAGAAGGAGACCATGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTTGGGAAGCTGAATATATCTCGACCTTTTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTTTTCATGGTGCGGGCTTTTGCCCTGAGTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGCAGATCGGTTCCTGAATCACATAGGGCTATAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATAATCAAGCATTTATGTCTTACTCTAAGAATTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATATCGACAACTCCGGGAATAATGGTGCAAACAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGCGCAGCTTGTCGGTGGAGCAGCTACGGACGTTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAATCTATTGAAGAGGGGAAGAGAAGCATGTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	CACGGGGCTTGTGCTCATACTATCGAATGTATGAGG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCAGCCCTCAAATTTGAGAGGGCTGATTATTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATTGTAAGAGAGGATTCTTCCTTCATAAAACGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGAACCACCTAATTGGGAGAAAGAAGAATTTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGATGAGGCATTTCTTTCCTCTGCTGCCTTTTTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	GCAACGGCGAATATTAAACTCTTCATAATAGTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGTTTGGAGCGGTATATAGAAAAGAATCGGATCGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGTGATGACGGCGAATAATCTTAGTTTCATGTTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CCATATTCCTTTTGCTTTTGGTTACGGCTGTGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAATCGCGTATTGGATACTATCGACATTTACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATGGGTAAAAGTTAATGGGCGCAGTTTTGCGCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCAGGGCGACAAGGGCGCCCGATCCCTCGGAGAGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAGACCGAACACTTTCAAATTTGACAGGTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAGACCTCGACGTTATAGACGCGCGCCTTCGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTCGATGTAATATCTTCGGGGTTAATTTCTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGCCGCGCAGGCTATCTCATATCGTCTCTTTTCCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGGATAGGGTTTGCCGCGACACTTTGACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTGTCTACATAGTGTTTAAGATAATGCTCAAAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTAACAGTCTTTAAGACTTACATTAAAGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCGGAATCGGCGCAAAGGACTACGCAGAAGGAAGCCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATTTGGCATGAGATGTCTTTTATTTCGACATCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGAAAACTCAAATAGTTTGATGATTTATTGCATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	GATTTTCTGGTACTTGATGATTATTATAGTAGCACA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACCAAGACCTTATAAAGCTCTTCCACAAGGTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCTGTTTCTTTCTACTAAAGCTGTCGTTTTCATAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAAAATATCGAACGCTAAAATTTAAAAACGAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTACTCACGCTTTATGCCGGCTCCTCATACTCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATGATGAGAAGTGCTGCGAACCCTTCAACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCACGATATATATCGTCACCCTGAGAAGCCGGGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATACGTCGGCTTTTCGGTATATGGCCCTATCAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATTGAAAATAGAAAGAACGAAAAAGAAATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTTGCGTATCAGGATCGTGCGACTCTTGTAGCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCTTGAATAACTACATTAGCATCAATAGGAACGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAAGTATTCTCCTCGATAGTAGAAATAATGCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTTGGGTCTATAGAATCTCCGTCCTCCAAAGGGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGTGAAAATATACTCCAGACTAGGTTAGAAAGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGCTACTGCGATAGTAGAAATAATGCTAACTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGTTTATGTTATTGGCTTAGAGCGTAAAAGGTTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CGATCGATCAGTCGATTACAGCAGCTCAAAGCCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATCGCGACCATCGATGACGAACGCCGCCTTCGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTATACATGTGTATAGAATCTTCTTGCCATTAAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAACACATCACTCTGCATGATCTGAGCATGGTAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGGGGAGGATACACGGATACGGCAGGTGAAATCGTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGAATAATCAATGGAAGAATTAGAATGGATTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	GTTCTCGTTCTTTCTGAGCTTGATGTAGGGATCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCCTGCGGCCTTATTTTCGTCGGCGTTGTGCTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTCGGCACACTCTTTGTAGCCGAACACTCGCCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCGTTTCTGAAGAATACGCTTTTTCATATTGCTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTCGCGGCAAGGGCAAATCCACCGATCCCGCCGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAATTCTTTTGAGACTATTAAAACAGGAGCTCTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAGCCTATTGCAGAGCTTACAGTCGAACTGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGACGGAGGTAAAGGGCTTTCAGGAGCAAGGCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCTCAGCCCGTCTATCAAGTGGGTGGGCACAAGTC
ATTTCAATTGCACCATACAGGAATTAAAAT	GTCGGTCGAGACTACGAGGACTTCCGGCTCAGGGAA


>NZ_CP024595|5|5|2271481-2282122|CRISPRCasFinder
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTGGGAATTACGATGAAGAAAAGCATTTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGCTCGTATATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATCTTCTTTAGTAAAGAATCTAAAAAGATCTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACAACGAGCTTTATTTGAGAAGTATATAAATACTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATACTATTATATTCTCGTTGTTCTGTATAGATAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAAACGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGCATCGATATGTTCCCTGTTTCTTGATGTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGTACTATTGCAATAGCATAACCATTGTGCTAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAACAACATCGATGTATTTTTGTAGACGTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TACGGTATAGAGTCTCAAGTACGTTGACTTCGGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGTGCTAAGAGAAACTTAATGCTGTTATATTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGTTCGTATATCGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTATCTTTTTCACTTGAGGTAGCATCAACAAACTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCAACCTCTTCATATCTACTGGATAGTTGAAGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TATAATTCTTTAGGAGATAGTCCAGGATCTACATCA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGGAGGATGAGGAGTTTTTGAATAACTACATCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTCAGGTTGGTATCCATATGCCTCTAAGAGGCTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGAGAGCGGGTGATATGATTGTAAGACTCAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GATGTGAAGTTCTCCAGCACACCTTCGAGAGTGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGATAACTTCACGCTCAGAAAGATTGACTGGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGGCGCAGATAGGGCTTAGAACCCTATCTGCTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GACAGGATATGCTATAGTTGCAAATTGAGTATATTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCTAGGATATATAGGACAATAATATTCACTGTCCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAACATCTCATGAGAGAATGTATAAATAGGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	CGTATTGTTCGCGTAGTTTGTTGTAATACTCAGCG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATGCCTCTAAGAGGCTGGATACTTCGATGGGTACG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAACAAAGGCTTGTGAGTATATGGCATTTCTATACCC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCACGTGTCCCATATGCCATAAAACGCGAACCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCATAAGTTCTATAGATTCTAGTTTAATTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TATCGTTTTGTAGGTTAAATAGCCTCTCTATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAGGGAGGTAACAAACCCCTGGGTAATAGAAAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGAAAGATTATAAACTTTCTAGATCCATATCTGCTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTAGTAATTAAATCTATTATAAATCATATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACTCCCTTATTAAAGACGTAGATCCGGCAGCTGC
ATTTCAATTGCACCATACAGGAATTAAAAC	ATAGGTAATGTAGTTCTCAGCTCTCGAACGGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTCTTGTGTGTGGATCTGCTCCTGATAATCCATCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TACTGTTGTTTTGTTAAACTTTTATTTTATGTCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCTTAAACTCAGATAAATCTACTTCTAAATTTAGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGGGATTATCAAAATAGCGATGTTTTACATCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGGTTCACTAACTGGCGGAATAAGTGTGATTCCACC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGAAATCTACAATACTTCCAACTTATTCAAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGATAGACATATGAAGAGCTTCAGACAGTGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGACTCGATAACCTCTTTCACAGAGTTCTCAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGCATTCTGTAGGAGCGAAGTTTTGTTTGTTTGTGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTGAACTTTCGGTTGAGCTAATACAAAGATT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTATAATGGAGTTAATATCAATCTGATTAAGAGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTGCAAATCTGTAAAAGTCTTTTTGGAATTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGACTGGATTAAGATGGATAAGGAAGGAAATTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTAAACGTAGATTATAAAACTCTACCGCTGTAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCTCATCGGTATGCTGCAAGAAAAAGATACACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATAAAGACCCTCAAAGAGGAGGGATTTAATATA
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGCTATACAGGTAATTTCTGCCTATTCGGCTTACC
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAAATGATCAAAAAGGAGTTTATCCACCGCAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCTTTTGCTTCTTTCTGATTGCGAGCGAATACG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACATCATCTGTATAGAGTTTATATGTGTCGTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTATTACGTTATAGAAATCATCTTCATCTGCTAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTGGTATTACAATAAAGAATCGATGTTTTTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTAACGCTGCTTCTATAAAAAGTTTTAGCCCTCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAATTAGGAACCTATAAAGAAGAGGAATAGATATGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTCCTCTACATCCTCAGGAGAAGGAGACCATGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTTGGGAAGCTGAATATATCTCGACCTTTTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTTTTCATGGTGCGGGCTTTTGCCCTGAGTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGCAGATCGGTTCCTGAATCACATAGGGCTATAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATAATCAAGCATTTATGTCTTACTCTAAGAATTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATATCGACAACTCCGGGAATAATGGTGCAAACAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGCGCAGCTTGTCGGTGGAGCAGCTACGGACGTTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAATCTATTGAAGAGGGGAAGAGAAGCATGTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	CACGGGGCTTGTGCTCATACTATCGAATGTATGAGG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCAGCCCTCAAATTTGAGAGGGCTGATTATTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATTGTAAGAGAGGATTCTTCCTTCATAAAACGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGAACCACCTAATTGGGAGAAAGAAGAATTTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGATGAGGCATTTCTTTCCTCTGCTGCCTTTTTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	GCAACGGCGAATATTAAACTCTTCATAATAGTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGTTTGGAGCGGTATATAGAAAAGAATCGGATCGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGTGATGACGGCGAATAATCTTAGTTTCATGTTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CCATATTCCTTTTGCTTTTGGTTACGGCTGTGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAATCGCGTATTGGATACTATCGACATTTACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATGGGTAAAAGTTAATGGGCGCAGTTTTGCGCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCAGGGCGACAAGGGCGCCCGATCCCTCGGAGAGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAGACCGAACACTTTCAAATTTGACAGGTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAGACCTCGACGTTATAGACGCGCGCCTTCGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTCGATGTAATATCTTCGGGGTTAATTTCTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGCCGCGCAGGCTATCTCATATCGTCTCTTTTCCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGGATAGGGTTTGCCGCGACACTTTGACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTGTCTACATAGTGTTTAAGATAATGCTCAAAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTAACAGTCTTTAAGACTTACATTAAAGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCGGAATCGGCGCAAAGGACTACGCAGAAGGAAGCCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATTTGGCATGAGATGTCTTTTATTTCGACATCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGAAAACTCAAATAGTTTGATGATTTATTGCATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	GATTTTCTGGTACTTGATGATTATTATAGTAGCACA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACCAAGACCTTATAAAGCTCTTCCACAAGGTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCTGTTTCTTTCTACTAAAGCTGTCGTTTTCATAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAAAATATCGAACGCTAAAATTTAAAAACGAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTACTCACGCTTTATGCCGGCTCCTCATACTCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATGATGAGAAGTGCTGCGAACCCTTCAACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCACGATATATATCGTCACCCTGAGAAGCCGGGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATACGTCGGCTTTTCGGTATATGGCCCTATCAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATTGAAAATAGAAAGAACGAAAAAGAAATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTTGCGTATCAGGATCGTGCGACTCTTGTAGCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCTTGAATAACTACATTAGCATCAATAGGAACGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAAGTATTCTCCTCGATAGTAGAAATAATGCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTTGGGTCTATAGAATCTCCGTCCTCCAAAGGGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGTGAAAATATACTCCAGACTAGGTTAGAAAGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGCTACTGCGATAGTAGAAATAATGCTAACTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGTTTATGTTATTGGCTTAGAGCGTAAAAGGTTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CGATCGATCAGTCGATTACAGCAGCTCAAAGCCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATCGCGACCATCGATGACGAACGCCGCCTTCGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTATACATGTGTATAGAATCTTCTTGCCATTAAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAACACATCACTCTGCATGATCTGAGCATGGTAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGGGGAGGATACACGGATACGGCAGGTGAAATCGTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGAATAATCAATGGAAGAATTAGAATGGATTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	GTTCTCGTTCTTTCTGAGCTTGATGTAGGGATCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCCTGCGGCCTTATTTTCGTCGGCGTTGTGCTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTCGGCACACTCTTTGTAGCCGAACACTCGCCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCGTTTCTGAAGAATACGCTTTTTCATATTGCTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTCGCGGCAAGGGCAAATCCACCGATCCCGCCGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAATTCTTTTGAGACTATTAAAACAGGAGCTCTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAGCCTATTGCAGAGCTTACAGTCGAACTGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGACGGAGGTAAAGGGCTTTCAGGAGCAAGGCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCTCAGCCCGTCTATCAAGTGGGTGGGCACAAGTC
ATTTCAATTGCACCATACAGGAATTAAAAT	GTCGGTCGAGACTACGAGGACTTCCGGCTCAGGGAA
ATTTCAATTGCACCATACAGGAATTAAAAT

>NZ_CP024595|5|3|2271481-2282122|CRT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTGGGAATTACGATGAAGAAAAGCATTTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGCTCGTATATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATCTTCTTTAGTAAAGAATCTAAAAAGATCTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACAACGAGCTTTATTTGAGAAGTATATAAATACTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATACTATTATATTCTCGTTGTTCTGTATAGATAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAAACGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGCATCGATATGTTCCCTGTTTCTTGATGTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGTACTATTGCAATAGCATAACCATTGTGCTAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAACAACATCGATGTATTTTTGTAGACGTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TACGGTATAGAGTCTCAAGTACGTTGACTTCGGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGTGCTAAGAGAAACTTAATGCTGTTATATTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGTTCGTATATCGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTATCTTTTTCACTTGAGGTAGCATCAACAAACTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCAACCTCTTCATATCTACTGGATAGTTGAAGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TATAATTCTTTAGGAGATAGTCCAGGATCTACATCA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGGAGGATGAGGAGTTTTTGAATAACTACATCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTCAGGTTGGTATCCATATGCCTCTAAGAGGCTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGAGAGCGGGTGATATGATTGTAAGACTCAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GATGTGAAGTTCTCCAGCACACCTTCGAGAGTGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGATAACTTCACGCTCAGAAAGATTGACTGGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGGCGCAGATAGGGCTTAGAACCCTATCTGCTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GACAGGATATGCTATAGTTGCAAATTGAGTATATTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCTAGGATATATAGGACAATAATATTCACTGTCCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAACATCTCATGAGAGAATGTATAAATAGGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	CGTATTGTTCGCGTAGTTTGTTGTAATACTCAGCG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATGCCTCTAAGAGGCTGGATACTTCGATGGGTACG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAACAAAGGCTTGTGAGTATATGGCATTTCTATACCC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCACGTGTCCCATATGCCATAAAACGCGAACCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCATAAGTTCTATAGATTCTAGTTTAATTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TATCGTTTTGTAGGTTAAATAGCCTCTCTATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAGGGAGGTAACAAACCCCTGGGTAATAGAAAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGAAAGATTATAAACTTTCTAGATCCATATCTGCTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTAGTAATTAAATCTATTATAAATCATATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACTCCCTTATTAAAGACGTAGATCCGGCAGCTGC
ATTTCAATTGCACCATACAGGAATTAAAAC	ATAGGTAATGTAGTTCTCAGCTCTCGAACGGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTCTTGTGTGTGGATCTGCTCCTGATAATCCATCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TACTGTTGTTTTGTTAAACTTTTATTTTATGTCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCTTAAACTCAGATAAATCTACTTCTAAATTTAGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGGGATTATCAAAATAGCGATGTTTTACATCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGGTTCACTAACTGGCGGAATAAGTGTGATTCCACC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGAAATCTACAATACTTCCAACTTATTCAAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGATAGACATATGAAGAGCTTCAGACAGTGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGACTCGATAACCTCTTTCACAGAGTTCTCAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGCATTCTGTAGGAGCGAAGTTTTGTTTGTTTGTGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTGAACTTTCGGTTGAGCTAATACAAAGATT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTATAATGGAGTTAATATCAATCTGATTAAGAGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTGCAAATCTGTAAAAGTCTTTTTGGAATTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGACTGGATTAAGATGGATAAGGAAGGAAATTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTAAACGTAGATTATAAAACTCTACCGCTGTAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCTCATCGGTATGCTGCAAGAAAAAGATACACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATAAAGACCCTCAAAGAGGAGGGATTTAATATA
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGCTATACAGGTAATTTCTGCCTATTCGGCTTACC
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAAATGATCAAAAAGGAGTTTATCCACCGCAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCTTTTGCTTCTTTCTGATTGCGAGCGAATACG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACATCATCTGTATAGAGTTTATATGTGTCGTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTATTACGTTATAGAAATCATCTTCATCTGCTAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTGGTATTACAATAAAGAATCGATGTTTTTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTAACGCTGCTTCTATAAAAAGTTTTAGCCCTCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAATTAGGAACCTATAAAGAAGAGGAATAGATATGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTCCTCTACATCCTCAGGAGAAGGAGACCATGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTTGGGAAGCTGAATATATCTCGACCTTTTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTTTTCATGGTGCGGGCTTTTGCCCTGAGTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGCAGATCGGTTCCTGAATCACATAGGGCTATAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATAATCAAGCATTTATGTCTTACTCTAAGA
ATTTCAATTTCAATTGCACCATACAGGAAT	TAAAACATATATCGACAACTCCGGGAATAATGGTGCAAACAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGCGCAGCTTGTCGGTGGAGCAGCTACGGACGTTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAATCTATTGAAGAGGGGAAGAGAAGCATGTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	CACGGGGCTTGTGCTCATACTATCGAATGTATGAGG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCAGCCCTCAAATTTGAGAGGGCTGATTATTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATTGTAAGAGAGGATTCTTCCTTCATAAAACGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGAACCACCTAATTGGGAGAAAGAAGAATTTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGATGAGGCATTTCTTTCCTCTGCTGCCTTTTTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	GCAACGGCGAATATTAAACTCTTCATAATAGTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGTTTGGAGCGGTATATAGAAAAGAATCGGATCGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGTGATGACGGCGAATAATCTTAGTTTCATGTTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CCATATTCCTTTTGCTTTTGGTTACGGCTGTGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAATCGCGTATTGGATACTATCGACATTTACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATGGGTAAAAGTTAATGGGCGCAGTTTTGCGCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCAGGGCGACAAGGGCGCCCGATCCCTCGGAGAGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAGACCGAACACTTTCAAATTTGACAGGTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAGACCTCGACGTTATAGACGCGCGCCTTCGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTCGATGTAATATCTTCGGGGTTAATTTCTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGCCGCGCAGGCTATCTCATATCGTCTCTTTTCCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGGATAGGGTTTGCCGCGACACTTTGACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTGTCTACATAGTGTTTAAGATAATGCTCAAAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTAACAGTCTTTAAGACTTACATTAAAGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCGGAATCGGCGCAAAGGACTACGCAGAAGGAAGCCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATTTGGCATGAGATGTCTTTTATTTCGACATCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGAAAACTCAAATAGTTTGATGATTTATTGCATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	GATTTTCTGGTACTTGATGATTATTATAGTAGCACA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACCAAGACCTTATAAAGCTCTTCCACAAGGTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCTGTTTCTTTCTACTAAAGCTGTCGTTTTCATAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAAAATATCGAACGCTAAAATTTAAAAACGAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTACTCACGCTTTATGCCGGCTCCTCATACTCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATGATGAGAAGTGCTGCGAACCCTTCAACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCACGATATATATCGTCACCCTGAGAAGCCGGGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATACGTCGGCTTTTCGGTATATGGCCCTATCAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATTGAAAATAGAAAGAACGAAAAAGAAATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTTGCGTATCAGGATCGTGCGACTCTTGTAGCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCTTGAATAACTACATTAGCATCAATAGGAACGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAAGTATTCTCCTCGATAGTAGAAATAATGCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTTGGGTCTATAGAATCTCCGTCCTCCAAAGGGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGTGAAAATATACTCCAGACTAGGTTAGAAAGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGCTACTGCGATAGTAGAAATAATGCTAACTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGTTTATGTTATTGGCTTAGAGCGTAAAAGGTTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CGATCGATCAGTCGATTACAGCAGCTCAAAGCCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATCGCGACCATCGATGACGAACGCCGCCTTCGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTATACATGTGTATAGAATCTTCTTGCCATTAAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAACACATCACTCTGCATGATCTGAGCATGGTAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGGGGAGGATACACGGATACGGCAGGTGAAATCGTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGAATAATCAATGGAAGAATTAGAATGGATTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	GTTCTCGTTCTTTCTGAGCTTGATGTAGGGATCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCCTGCGGCCTTATTTTCGTCGGCGTTGTGCTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTCGGCACACTCTTTGTAGCCGAACACTCGCCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCGTTTCTGAAGAATACGCTTTTTCATATTGCTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTCGCGGCAAGGGCAAATCCACCGATCCCGCCGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAATTCTTTTGAGACTATTAAAACAGGAGCTCTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAGCCTATTGCAGAGCTTACAGTCGAACTGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGACGGAGGTAAAGGGCTTTCAGGAGCAAGGCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCTCAGCCCGTCTATCAAGTGGGTGGGCACAAGTC
ATTTCAATTGCACCATACAGGAATTAAAAT	GTCGGTCGAGACTACGAGGACTTCCGGCTCAGGGAA
ATTTCAATTGCACCATACAGGAATTAAAAT

>NZ_CP024595|5|4|2273065-2282122|PILER-CR
	AATTTGGGAATTACGATGAAGAAAAGCATTTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGCTCGTATATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATCTTCTTTAGTAAAGAATCTAAAAAGATCTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACAACGAGCTTTATTTGAGAAGTATATAAATACTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AATACTATTATATTCTCGTTGTTCTGTATAGATAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAAACGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTGCTGAACAAAAAGAAACAATTCGTAAGTTTCTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAAAATCGTGTTCAATCGGAACCTCTTTTATAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGCATCGATATGTTCCCTGTTTCTTGATGTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGTACTATTGCAATAGCATAACCATTGTGCTAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAACAACATCGATGTATTTTTGTAGACGTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTAAAGGTTCAAGGCTCGGTAGAAATGGGGGGAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TACGGTATAGAGTCTCAAGTACGTTGACTTCGGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGTGCTAAGAGAAACTTAATGCTGTTATATTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAATTAGAATCTTTTATTCGTTCGTATATCGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTATCTTTTTCACTTGAGGTAGCATCAACAAACTT
ATTTCAATTGCACCATACAGGAATTAAAACATCAACCTCTTCATATCTACTGGATAGTTGAAGTTATTTCAATTGCACCATACAGGAATTAAAACTATAATTCTTTAGGAGATAGTCCAGGATCTACATCAATTTCAATTGCACCATACAGGAATTAAAAC	AAGGAGGATGAGGAGTTTTTGAATAACTACATCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTCAGGTTGGTATCCATATGCCTCTAAGAGGCTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGAGAGCGGGTGATATGATTGTAAGACTCAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GATGTGAAGTTCTCCAGCACACCTTCGAGAGTGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGATAACTTCACGCTCAGAAAGATTGACTGGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGGCGCAGATAGGGCTTAGAACCCTATCTGCTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GACAGGATATGCTATAGTTGCAAATTGAGTATATTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCTAGGATATATAGGACAATAATATTCACTGTCCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCAACATCTCATGAGAGAATGTATAAATAGGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	CGTATTGTTCGCGTAGTTTGTTGTAATACTCAGCG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATGCCTCTAAGAGGCTGGATACTTCGATGGGTACG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAACAAAGGCTTGTGAGTATATGGCATTTCTATACCC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCACGTGTCCCATATGCCATAAAACGCGAACCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCATAAGTTCTATAGATTCTAGTTTAATTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TATCGTTTTGTAGGTTAAATAGCCTCTCTATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAGGGAGGTAACAAACCCCTGGGTAATAGAAAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGAAAGATTATAAACTTTCTAGATCCATATCTGCTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTAGTAATTAAATCTATTATAAATCATATTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACTCCCTTATTAAAGACGTAGATCCGGCAGCTGC
ATTTCAATTGCACCATACAGGAATTAAAAC	ATAGGTAATGTAGTTCTCAGCTCTCGAACGGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	GTCTTGTGTGTGGATCTGCTCCTGATAATCCATCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TACTGTTGTTTTGTTAAACTTTTATTTTATGTCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCTTAAACTCAGATAAATCTACTTCTAAATTTAGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGGGATTATCAAAATAGCGATGTTTTACATCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGGTTCACTAACTGGCGGAATAAGTGTGATTCCACC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGAAATCTACAATACTTCCAACTTATTCAAGAAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGATAGACATATGAAGAGCTTCAGACAGTGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGACTCGATAACCTCTTTCACAGAGTTCTCAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGCATTCTGTAGGAGCGAAGTTTTGTTTGTTTGTGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTGAACTTTCGGTTGAGCTAATACAAAGATT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTATAATGGAGTTAATATCAATCTGATTAAGAGCAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTGCAAATCTGTAAAAGTCTTTTTGGAATTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGACTGGATTAAGATGGATAAGGAAGGAAATTTAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AACTTAAACGTAGATTATAAAACTCTACCGCTGTAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGCTCATCGGTATGCTGCAAGAAAAAGATACACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATAAAGACCCTCAAAGAGGAGGGATTTAATATA
ATTTCAATTGCACCATACAGGAATTAAAAC	GAGGCTATACAGGTAATTTCTGCCTATTCGGCTTACC
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAAATGATCAAAAAGGAGTTTATCCACCGCAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCTTTTGCTTCTTTCTGATTGCGAGCGAATACG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACACATCATCTGTATAGAGTTTATATGTGTCGTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTATTACGTTATAGAAATCATCTTCATCTGCTAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTGGTATTACAATAAAGAATCGATGTTTTTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTAACGCTGCTTCTATAAAAAGTTTTAGCCCTCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAATTAGGAACCTATAAAGAAGAGGAATAGATATGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTCCTCTACATCCTCAGGAGAAGGAGACCATGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTTGGGAAGCTGAATATATCTCGACCTTTTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTTTTCATGGTGCGGGCTTTTGCCCTGAGTTCTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGCAGATCGGTTCCTGAATCACATAGGGCTATAG
ATTTCAATTGCACCATACAGGAATTAAAAC	TATAATCAAGCATTTATGTCTTACTCTAAGAATTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATATCGACAACTCCGGGAATAATGGTGCAAACAC
ATTTCAATTGCACCATACAGGAATTAAAAC	AAGCGCAGCTTGTCGGTGGAGCAGCTACGGACGTTGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCAATCTATTGAAGAGGGGAAGAGAAGCATGTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	CACGGGGCTTGTGCTCATACTATCGAATGTATGAGG
ATTTCAATTGCACCATACAGGAATTAAAAC	TTTCAGCCCTCAAATTTGAGAGGGCTGATTATTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATTGTAAGAGAGGATTCTTCCTTCATAAAACGTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TTGAACCACCTAATTGGGAGAAAGAAGAATTTTATA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGATGAGGCATTTCTTTCCTCTGCTGCCTTTTTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	GCAACGGCGAATATTAAACTCTTCATAATAGTTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAGTTTGGAGCGGTATATAGAAAAGAATCGGATCGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGTGATGACGGCGAATAATCTTAGTTTCATGTTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CCATATTCCTTTTGCTTTTGGTTACGGCTGTGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAATCGCGTATTGGATACTATCGACATTTACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATGGGTAAAAGTTAATGGGCGCAGTTTTGCGCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCAGGGCGACAAGGGCGCCCGATCCCTCGGAGAGGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTGCAGACCGAACACTTTCAAATTTGACAGGTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGAGACCTCGACGTTATAGACGCGCGCCTTCGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTCGATGTAATATCTTCGGGGTTAATTTCTTCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGCCGCGCAGGCTATCTCATATCGTCTCTTTTCCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTGGATAGGGTTTGCCGCGACACTTTGACGCGCT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTGTCTACATAGTGTTTAAGATAATGCTCAAAAAG
ATTTCAATTGCACCATACAGGAATTAAAAC	AATTTTAACAGTCTTTAAGACTTACATTAAAGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	CCGGAATCGGCGCAAAGGACTACGCAGAAGGAAGCCA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATTTGGCATGAGATGTCTTTTATTTCGACATCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTT
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACA
ATTTCAATTGCACCATACAGGAATTAAAAC	CTGAAAACTCAAATAGTTTGATGATTTATTGCATA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	GATTTTCTGGTACTTGATGATTATTATAGTAGCACA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCATTAAAAATATCATCTGTATGTAGCTGCAGTACAT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAGTAACGACTTAAATACATAATAATCTGAAATTTT
ATTTCAATTGCACCATACAGGAATTAAAAC	AGATTCTTATTATAATTATTTCTTATCGTACTTAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GAACCAAGACCTTATAAAGCTCTTCCACAAGGTTG
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCTGTTTCTTTCTACTAAAGCTGTCGTTTTCATAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAAAATATCGAACGCTAAAATTTAAAAACGAAGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGTACTCACGCTTTATGCCGGCTCCTCATACTCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGATGATGAGAAGTGCTGCGAACCCTTCAACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCACGATATATATCGTCACCCTGAGAAGCCGGGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCACGAACAAGACGCAGCTGATAAGCGCAATCAACT
ATTTCAATTGCACCATACAGGAATTAAAAC	ACATAGCACGGTTTATCTACAGAGACAACTCCTCAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAGTATCAGAGGCGATGGAGATTGAAGCAATCTTCC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTCGTGCCGTCGGGGGTTACGGCGACCCTTGGCAAT
ATTTCAATTGCACCATACAGGAATTAAAAC	AAAAAAGAAGAATAACCATGTTAGGAGCGATAATTG
ATTTCAATTGCACCATACAGGAATTAAAAC	TCGAAAGGGACAACGCTTTCGACAGGCTGGCGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	AGTTTTGTACCCCTCGACGTTCTCGCGTAGCGTAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TTATAGATGTGTCCATTTTTGAAGTGGTAACCTGCGCTG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATACGTCGGCTTTTCGGTATATGGCCCTATCAATG
ATTTCAATTGCACCATACAGGAATTAAAAC	ATATTGAAAATAGAAAGAACGAAAAAGAAATCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACTTATGTTCTTTTCGATACCGGATAGTTCAAGCAGC
ATTTCAATTGCACCATACAGGAATTAAAAC	TATACTCTGTTACGTCCATCTTGTTAGATGAACAAG
ATTCCAATTGCACCATACAGGAATTAAAAC	AGAGAGAATCGTATATTTCAATCGATCCGCCACTGG
ATTTCAATTGCACCATACAGGAATTAAAAC	CTTTGCGTATCAGGATCGTGCGACTCTTGTAGCTGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGCTTGAATAACTACATTAGCATCAATAGGAACGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TAAAGTATTCTCCTCGATAGTAGAAATAATGCTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATGTTGGGTCTATAGAATCTCCGTCCTCCAAAGGGG
ATTTCAATTGCACCATACAGGAATTAAAAC	GGTGAAAATATACTCCAGACTAGGTTAGAAAGGAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACAGCTACTGCGATAGTAGAAATAATGCTAACTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGTTTATGTTATTGGCTTAGAGCGTAAAAGGTTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	CGATCGATCAGTCGATTACAGCAGCTCAAAGCCTCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCATCGCGACCATCGATGACGAACGCCGCCTTCGTA
ATTTCAATTGCACCATACAGGAATTAAAAC	TCTATACATGTGTATAGAATCTTCTTGCCATTAAAC
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAACACATCACTCTGCATGATCTGAGCATGGTAGT
ATTTCAATTGCACCATACAGGAATTAAAAC	TGGGGAGGATACACGGATACGGCAGGTGAAATCGTC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGAATAATCAATGGAAGAATTAGAATGGATTTTTC
ATTTCAATTGCACCATACAGGAATTAAAAC	GTTCTCGTTCTTTCTGAGCTTGATGTAGGGATCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	CGCCTGCGGCCTTATTTTCGTCGGCGTTGTGCTAT
ATTTCAATTGCACCATACAGGAATTAAAAC	CAGCTCGGCACACTCTTTGTAGCCGAACACTCGCCG
ATTTCAATTGCACCATACAGGAATTAAAAC	GCGTTTCTGAAGAATACGCTTTTTCATATTGCTCTC
ATTTCAATTGCACCATACAGGAATTAAAAC	CCTCGCGGCAAGGGCAAATCCACCGATCCCGCCGA
ATTTCAATTGCACCATACAGGAATTAAAAC	TGAATTCTTTTGAGACTATTAAAACAGGAGCTCTTA
ATTTCAATTGCACCATACAGGAATTAAAAC	ACGAGCCTATTGCAGAGCTTACAGTCGAACTGCGGC
ATTTCAATTGCACCATACAGGAATTAAAAC	AGACGGAGGTAAAGGGCTTTCAGGAGCAAGGCGAAA
ATTTCAATTGCACCATACAGGAATTAAAAC	ATCTCAGCCCGTCTATCAAGTGGGTGGGCACAAGTC
ATTTCAATTGCACCATACAGGAATTAAAAT	GTCGGTCGAGACTACGAGGACTTCCGGCTCAGGGAA
ATTTCAATTGCACCATACAGGAATTAAAAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024595.1\|WP_099779613.1\|2284717_2286466_-\|phospho-sugar-mutase	unknown	unknown	gnl\|CDD\|100092
NZ_CP024595.1\|WP_099779610.1\|2269955_2270972_+\|type-I-B-CRISPR-associated-endonuclease-Cas1	cas1	cd09722_cas1_CAS-I-B	gnl\|CDD\|274695
NZ_CP024595.1\|WP_012458630.1\|2296180_2296807_+\|signal-peptidase-I	unknown	unknown	gnl\|CDD\|274044
NZ_CP024595.1\|WP_097616251.1\|2294061_2294778_+\|4-hydroxy-tetrahydrodipicolinate-reductase	unknown	unknown	gnl\|CDD\|234595
NZ_CP024595.1\|WP_021664493.1\|2292657_2294001_+\|deoxyguanosinetriphosphate-triphosphohydrolase-family-protein	unknown	unknown	gnl\|CDD\|273571
NZ_CP024595.1\|WP_099779611.1\|2282950_2283853_-\|IS982-like-element-IS195-family-transposase	unknown	unknown	gnl\|CDD\|372648
NZ_CP024595.1\|WP_012458648.1\|2264222_2264810_+\|hypothetical-protein	cas5	mkCas0069_cas5_CAS-I-B	unknown
NZ_CP024595.1\|WP_088442951.1\|2291521_2292514_+\|putative-sulfate-exporter-family-transporter	unknown	unknown	gnl\|CDD\|225411
NZ_CP024595.1\|WP_054191585.1\|2286538_2287276_-\|DNA-repair-protein-RecO	unknown	unknown	gnl\|CDD\|376822
NZ_CP024595.1\|WP_012458635.1\|2290653_2291013_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_012458646.1\|2266957_2268253_+\|hypothetical-protein	cas8b6	mkCas0111_cas8b6_CAS-I-B	unknown
NZ_CP024595.1\|WP_004583651.1\|2294793_2296191_+\|signal-peptidase-I	unknown	unknown	gnl\|CDD\|182787
NZ_CP024595.1\|WP_157766537.1\|2263217_2263310_-\|DUF1661-domain-containing-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_010956473.1\|2270971_2271235_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_CP024595.1\|WP_012458649.1\|2263550_2264216_+\|CRISPR-associated-endoribonuclease-Cas6	cas6	cd09652_cas6_CAS-I:CAS-III	gnl\|CDD\|273848
NZ_CP024595.1\|WP_099779615.1\|2287845_2290347_-\|TonB-dependent-receptor	unknown	unknown	gnl\|CDD\|238657
NZ_CP024595.1\|WP_099779607.1\|2263278_2263476_+\|DUF1661-domain-containing-protein	unknown	unknown	gnl\|CDD\|285160
NZ_CP024595.1\|WP_099779608.1\|2264826_2266947_+\|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|224124
NZ_CP024595.1\|WP_097552678.1\|2268273_2269332_+\|CRISPR-associated-protein-Cas7	cas7	mkCas0088_cas7_CAS-I-B	gnl\|CDD\|273846
NZ_CP024595.1\|WP_099779609.1\|2269449_2269959_+\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|366863

Protein	Function_ID	Function_description	E-value
NZ_CP024595.1\|WP_099779613.1\|2284717_2286466_-\|phospho-sugar-mutase	gnl\|CDD\|100092	cd05799, PGM2, This CD includes PGM2 (phosphoglucomutase 2) and PGM2L1 (phosphoglucomutase 2-like 1). The mammalian PGM2 is thought to be a phosphopentomutase that catalyzes the conversion of the nucleoside breakdown products, ribose-1-phosphate and deoxyribose-1-phosphate to the corresponding 5-phosphopentoses. PGM2L1 is thought to catalyze the 1,3-bisphosphoglycerate-dependent synthesis of glucose 1,6-bisphosphate and other aldose-bisphosphates that serve as cofactors for several sugar phosphomutases and possibly also as regulators of glycolytic enzymes. PGM2 and PGM2L1 belong to the alpha-D-phosphohexomutase superfamily which includes several related enzymes that catalyze a reversible intramolecular phosphoryl transfer on their sugar substrates. Other members of this superfamily include phosphoglucosamine mutase (PNGM), phosphoacetylglucosamine mutase (PAGM), the bacterial phosphomannomutase ManB, the bacterial phosphoglucosamine mutase GlmM, and the bifunctional phosphomannomutase/phosphoglucomutase (PMM/PGM). Each of these enzymes has four domains with a centrally located active site formed by four loops, one from each domain. All four domains are included in this alignment model.	0
NZ_CP024595.1\|WP_099779610.1\|2269955_2270972_+\|type-I-B-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274695	TIGR03641, cas1_HMARI, CRISPR-associated endonuclease Cas1, subtype I-B/HMARI/TNEAP. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes Cas1 subgroup that includes Cas1 proteins of the related HMARI and TNEAP subtypes of CRISPR/Cas system.	1.54491e-164
NZ_CP024595.1\|WP_012458630.1\|2296180_2296807_+\|signal-peptidase-I	gnl\|CDD\|274044	TIGR02227, Inactive_signal_peptidase_IA., signal peptidase I, bacterial type. This model represents signal peptidase I from most bacteria. Eukaryotic sequences are likely organellar. Several bacteria have multiple paralogs, but these represent isozymes of signal peptidase I. Virtually all known bacteria may be presumed to A related model finds a simlar protein in many archaea and a few bacteria, as well as a microsomal (endoplasmic reticulum) protein in eukaryotes. [Protein fate, Protein and peptide secretion and trafficking].	6.50616e-12
NZ_CP024595.1\|WP_097616251.1\|2294061_2294778_+\|4-hydroxy-tetrahydrodipicolinate-reductase	gnl\|CDD\|234595	PRK00048, PRK00048, dihydrodipicolinate reductase; Provisional.	2.23878e-51
NZ_CP024595.1\|WP_021664493.1\|2292657_2294001_+\|deoxyguanosinetriphosphate-triphosphohydrolase-family-protein	gnl\|CDD\|273571	TIGR01353, dGTP_triPase, deoxyguanosinetriphosphate triphosphohydrolase, putative. dGTP triphosphohydrolase (dgt) releases inorganic triphosphate, an unusual activity reaction product, from GTP. Its activity has been called limited to the Enterobacteriaceae, although homologous sequences are detected elsewhere. This finding casts doubt on whether the activity is shared in other species. In several of these other species, the homologous gene is found in an apparent operon with dnaG, the DNA primase gene. The enzyme from E. coli was shown to bind coopertatively to single stranded DNA. The biological role of dgt is unknown. [Purines, pyrimidines, nucleosides, and nucleotides, Nucleotide and nucleoside interconversions].	4.95914e-160
NZ_CP024595.1\|WP_099779611.1\|2282950_2283853_-\|IS982-like-element-IS195-family-transposase	gnl\|CDD\|372648	pfam13612, DDE_Tnp_1_3, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contains three carboxylate residues that are believed to be responsible for coordinating metal ions needed for catalysis. The catalytic activity of this enzyme involves DNA cleavage at a specific site followed by a strand transfer reaction.	4.32032e-99
NZ_CP024595.1\|WP_088442951.1\|2291521_2292514_+\|putative-sulfate-exporter-family-transporter	gnl\|CDD\|225411	COG2855, COG2855, Predicted membrane protein [Function unknown].	1.65319e-53
NZ_CP024595.1\|WP_054191585.1\|2286538_2287276_-\|DNA-repair-protein-RecO	gnl\|CDD\|376822	pfam02565, RecO_C, Recombination protein O C terminal. Recombination protein O (RecO) is involved in DNA repair and pfam00470 pathway recombination.	1.30559e-18
NZ_CP024595.1\|WP_004583651.1\|2294793_2296191_+\|signal-peptidase-I	gnl\|CDD\|182787	PRK10861, PRK10861, signal peptidase I.	8.0144e-17
NZ_CP024595.1\|WP_010956473.1\|2270971_2271235_+\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	2.04042e-30
NZ_CP024595.1\|WP_012458649.1\|2263550_2264216_+\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|273848	TIGR01877, CRISPR-associated_endoribonuclease_Cas6_1, CRISPR-associated endoribonuclease Cas6. CRISPR is a term for Clustered, Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This broadly distributed, highly divergent Cas family is now characterized as an endoribonuclease that generates guide RNAs for host defense against phage and other invaders. The family contains a C-terminal motif GXGXXXXXGXG, where the each X between two Gly is hydrophobic and the spacer XXXXX contains (usually) one Arg or Lys. The seed alignment for the current version of this model has gappy columns removed. Members of this protein family are found associated with several different CRISPR/cas system subtypes, and consequently we designate this family Cas6.	3.8915e-34
NZ_CP024595.1\|WP_099779615.1\|2287845_2290347_-\|TonB-dependent-receptor	gnl\|CDD\|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	5.53294e-41
NZ_CP024595.1\|WP_099779607.1\|2263278_2263476_+\|DUF1661-domain-containing-protein	gnl\|CDD\|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	2.6292e-05
NZ_CP024595.1\|WP_099779608.1\|2264826_2266947_+\|CRISPR-associated-helicase/endonuclease-Cas3	gnl\|CDD\|224124	COG1203, COG1203, CRISPR-associated helicase Cas3 [Defense mechanisms].	2.16595e-59
NZ_CP024595.1\|WP_097552678.1\|2268273_2269332_+\|CRISPR-associated-protein-Cas7	gnl\|CDD\|273846	TIGR01875, CRISPR-associated_protein_Cas7/Cst2/DevR, CRISPR-associated autoregulator DevR family. CRISPR is a term for Clustered Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This model represents one such family, represented by MJ0381 of Methanococcus jannaschii. This family includes the DevR protein of Myxococcus xanthus, a protein whose expression appears to regulated through a number of means, including both location and autorepression; DevR mutants are incapable of fruiting body development. [Regulatory functions, DNA interactions, , ].	0.000103036
NZ_CP024595.1\|WP_099779609.1\|2269449_2269959_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	2.43134e-68

>NZ_CP024595.1|WP_010956473.1|2270971_2271235_+|CRISPR-associated-endonuclease-Cas2
MYIILVYDIGEKRVGKMLKLCRKYLNWIQNSVFEGEISEVKLLELKSRAAGIMEKEEDSLIIFSSRQERWLEKEIIGKERSATDIFL
>NZ_CP024595.1|WP_099779610.1|2269955_2270972_+|type-I-B-CRISPR-associated-endonuclease-Cas1
MKKTYYLFNPGELSRKDNTIRFVPIQEGENGQEQAGQARYIPIEGISDFYVFGSLRANSSLYNFLGSNDIAVHFFDYYENYTGSFMPRDFLLSGKMLLAQASAYKNKKKRLFLARKFIEGAASNMQKNLAYYNNRGKDMQPMMELIDKYSLRLKETTTIEALMGIEGNIRQAYYDAFNLIIDPFEMGVRSKQPPQNEVNALISFGNMMCYTLCLKAIHQSQLNPTISFLHTPGERRYSLCLDISEVFKPILVDRTIFKVMNKRIIQAKHFDKQLNKCILNPSGKKLFVQAFEERLSETIRHRKLNRSVSFRHLVKLECYKIAKDILGIEEYQPFKMYW
>NZ_CP024595.1|WP_099779609.1|2269449_2269959_+|CRISPR-associated-protein-Cas4
MIITGTHFNYHQVCRRKLWLFSAGITMEHTSDLVYEGKLIHETTYQQRPERYQELELDGIKIDFYDAKNRVVHEVKKSNKISPAHRLQLLYYLYVLERNGVSGATGILEYPTLRKKEEVILSDIDRERIREIEQEILQIISHEDCPPVIDSGICKNCSYYEFCFSGEEQ
>NZ_CP024595.1|WP_097552678.1|2268273_2269332_+|CRISPR-associated-protein-Cas7
MKPYIYLRGLKRAEHTVFCVQDGQKTYYDAQYDRSLAYSSGQQVKRSVLEAFTDCLNVQMAPITFNYEISSKKELTQKEPWSPCDPEYADQLIGGWMRAGDGITKKRRSPLSVSAMRPLHPLLCGVSKENLTFDRSDRPDNHPVNVRLAGQSSLLSEEEIESFLRDTGSTLTRRHWIPDNKRASGLFVYDIAIDLRTLFSVSLNQHDPEIDPETIEKLRANGWVESETVFGKCLVLPKAGRDKIIPALAHALIHWRITSNQARTFSLMETLAIAISDKANAQAGAIRAKLVDDGSEKPKAKPIVDEKAGAELFITLPCAAHVVVENESADALDAAEKRLIEMLQAFDYENQL
>NZ_CP024595.1|WP_012458646.1|2266957_2268253_+|hypothetical-protein
MVTSVIGKIFLKAYNERNNTDYAPKGFFLDIYYPLFFGQEKYLMTAGNSPFENPKISWKDMILGKKHFETAERRAERLEKFVEKIDSGIADASIAIGYPSIDPLSTTSGQVSIPRNEIDASESYLSWIGAGLGVGVQGGMTILFNKPELLLDIFEGWKEYRRHLDKTPSMRGNQINTWNGQWIKKLYDSKDCSLDFSDVYSTKDGIMEVSILPWAQLLVSISKRFEDPKMMGYIYNIGQTNTTIGFIPFVLWPIRKANELFDRYFGADKYKDAVKLFGTAIGFAKACSEGSVGLKAMEPKGLSDYMRKGKIPVCKAGNEEQTIQYNTYQIWLLAMLNNEELWGKSKEFAQTLQLFGSGGKAGRTGRTNAIKLLLEATNKKVFIERLTAIVEESEVAKELEEMASIVHLMPSDNVPYFLTLIRFHYAVINKQ
>NZ_CP024595.1|WP_099779608.1|2264826_2266947_+|CRISPR-associated-helicase/endonuclease-Cas3
MSRYEHIFAKSDGTPLLQHLQDVAKAAEVMAQHWGLSTDMARKGAHLHDIGKASPIFQSRLKAEDNLGGDVFRHEIASIFFISLLPDEVDRRAIIEMIAAHHKSICNDSRELGLLDLDENESRCFKLHSKGFEQWSQEALGILHELGWETHPITMDEARSNYQEAVDYCSSLGRNCSQWKGLLMAADHFASSLDGQTEDTLRKLFVTPDLSYYRNRRSELYPLSLLSADDERQHTLVTAPTGAGKTDFLLRRCRGRVFYTLPFQASINAMYDRLKADLRDTDAQIYPLHAASILKLNGGYERILSRHVGASIKVLTPHQIAALAFGLKGYEVTALDIRGCDVILDEIHTYRKETQAMVLKIVEILVALGCRIHIGTATMPTDLYTGLLRLLGGETAVYEVKLPKEVLKGFDRHTIHKAGSMEDVEPVIQKAIEQSQKILMVCNQVTRAQQLYQEVVRKYPAIPTLLIHSRFKRGHRAQLEQELKERYNQCQGPCIVVSTQVVEVSLDISFDMMLTECAPIDALIQRFGRINRKRSLETIGQTKPIYVIAPPENEKEALPYELEILQRSYSSLPHCEVLHEADVQQLLDAVYPEVMALDINMHTIFQDGEWVMKELKHNSKSALFKILDINSACCIMESDREEYENGNYINRTPLEIPVPQSIRFKQLVATNCGAHPFVIPDRAYDSKLGLMEEFADSRYYKSFEIF
>NZ_CP024595.1|WP_012458648.1|2264222_2264810_+|hypothetical-protein
MEDKIFFVVHYTGPFGYIKPWSAVRDGETYSQQFLTPSIIEGMEKKLFPEMLIKKGIHKIARHKLSCMSMSVQQEKTQTQAWEGKGKGKGRTYTRPQSILKRGVMLHPSLYLAFTSEEDAVIAARQHLCLCRNEDVVLPDTEILKMDEETFNALPGFELRFGKDYPDAFMVGFNRFDENTPMYGRIEIGGEAILQ
>NZ_CP024595.1|WP_012458649.1|2263550_2264216_+|CRISPR-associated-endoribonuclease-Cas6
MRIELSIKADDSLVSFSHQHLLVGTLQKWLGENDMHGKSISYSFSRLNGGKFVSELNSILFTDWANMFVSAHDPELIRRMLAGIRQDPEMFKSLCVREVTVIEDPDMTDREIFFPAGPILLKRWREDNGFDHIVYTDEAANALLTENLRKKLQAVGIDDPTATASFVPDQGKAKVMLIDYRGVKNKASWCPIRIIGNAETKLFAWNAGIGNSTGIGFGAIK
>NZ_CP024595.1|WP_099779607.1|2263278_2263476_+|DUF1661-domain-containing-protein
MVREIKNSRATTKNFLFRFFRKHAPQSEHFRFVFYTPALAPFLFSVRFSQNSSERWMLYIRFPRK
>NZ_CP024595.1|WP_157766537.1|2263217_2263310_-|DUF1661-domain-containing-protein
MAREFFISRTTTKKFTRHVFRGRRHREIGS
>NZ_CP024595.1|WP_099779611.1|2282950_2283853_-|IS982-like-element-IS195-family-transposase
MKTNIVDVFCIIDDFSKLFDEAIKKKTLEEADKKRRNRKFKMSDSEVMTILILFHLSRYRDLKAFYLQYITHSCRSEFPHLVSYNRFVELQSRVGFKLIAFLNMCCLGQCTGISFIDSTPLKACHIKRAHGHRTMRGWAQKGKSTMGWFYGFKLHIVINDRGEIINYQITPGNCDDREPLKDGTFTKNLFGKLIADRGCISQNLFDRLFVDDIHMITKIKKNMKNSLMHLYDKVLLRKRALIETVNDMLKNVCQIEHTRHRSVNNFVTNLISGIIAYNILPKKPELNIEIIRNPNFPISA
>NZ_CP024595.1|WP_099779613.1|2284717_2286466_-|phospho-sugar-mutase
METDKLLDQVRAKARIWLGTEYDDSSRKAVQAMLDNADTTELVDAFYRDLEFGTGGLRGIMGAGTNRMNRYTVGAATQGLSNYLLREFAGSSDISVVIGYDCRNNSRFFADTAAAVFSANGIGVYLFEELRPTPEISYAIRHLGCKSGVMITASHNPKEYNGYKAYWEDGAQIIAPHDRNIIAEVNRIRSVDEIKFEAKPELIRMIGENIDSAFIAEVKALSLSPESIARHRDMKIVYTPIHGTGSTVVPRALREYGFANIIHVPEQDVVSGDFPTVHSPNPEEPAALALAIAKAEETGADLVLASDPDADRIGVAVRNNEGRMVLINGNEICSLLIYYSIMRRKELGDLHPDDYIVKTIVTTELIRDIAKKEHVSMFDCYTGFKWIAAVIRENEGRRRYIGGGEESYGFLWEDFIRDKSSVSACALFCEMAAWALDRGMSVYRLIRSIYLEYGLYYEKGLSVVRKGKSGAEEIEAMMRNYREYAPVELGGSPVQEILDYASLEGKDFTRGEKFSLDMPTTSNVLQYKTEDGTKVSIRPSGTEPKIKFYIGVHFSVANEQELDRAYTIAEEKIAAILHDLGV
>NZ_CP024595.1|WP_054191585.1|2286538_2287276_-|DNA-repair-protein-RecO
MIIVSRAIVLHNTAYNDSYSIAHLFSRESGRVSYLIPRSSKRGKSGGSLRLLISPLNELEITAEHKQHRDLHFIKEAKLCSLHGRIQSDPVRNSIALFLAEFLYLILRLPEADTNLYDFVAFSIDKLEEMDGPMANFHLAFLFRLLVPLGLIPDLQFGGSVIPRWFDPADGRFVPNAPAHGRGIPPHQSTYLQLFSRITFDNMKAFRLSRGERRQVLDYLVDYYRFHLPPFPLLKTPDILSTLFY
>NZ_CP024595.1|WP_099779615.1|2287845_2290347_-|TonB-dependent-receptor
MKQLNIISFIIAFLFLGTSASAQQSGGSVTGTVVDKSSKEPIAYVQVFVKGTTLGTSTDANGNYSIKGIPSGNQTIVARLMGYSTCEEKVHIEKGGSRHVDLYLTEEILSLDGVVVSANRNETFRRQAPSLVTVLSPELFLKTNSTNLSQGLKFQPGLRVEDNCQNCGFNQVRINGLEGAYSQILIDSHPIFSSLAGVYGLEQMPANMIERVEVIRGGGSALFGSNAVGGVINVITKEPLRNSAEISHSTMTFDHAKGWGSFQNTTQFNGSMLTEDRKAGVMVFGQHNYRPGQDIDGDSFTELPNLRNRSLGFRSYYKTGLYSKATLEYHSMQEYRRGGDRLDNPPFEAQIAEYLQHYINGGSFKFDQGFSGGKDFFSLYASAQDVQRRSYYGGGDYTENLLNGAVQSGSTESDEYNNAFTALTSYGTTKGFDLQGGGMYRHTFGENWDFTGGLEYIYGQLDDRSGYRPSKIDQNTSTFSQYDQLEYKTEKLSALIGARIDYVLLNQDGKRYIDPLFIFSPRANVRYNPNKNLCFRLSYSEGFRAPQYFDEDLHVELAGGTPISRVLSPNLKEERSRSISASFDYYHRADEWQFNIMGEAFSTFISNQFKPSDKVETTSDGKEWIIRTIYNDKDGVSKVYGVNLEGRIAYNKSFDLQLGGTWQRSRYGSIYTAVEADKTTGQAEISVKDYVRTPNLYGYFVATVRPTEHFAINLSGTFTGKMDVVHEAYEGDIPAEHIAPDGSFDFEMNGQQFKGLAEGHAKLVKTPTFADIDLKLSHDFHLASTMTLELNAGIQNIFNSYQKDTDKGPGRASTYVYGPMQPRRIFVGTKINF
>NZ_CP024595.1|WP_012458635.1|2290653_2291013_-|hypothetical-protein
MKERLNQTVRYFLPILFAVYAGLVISFTHVHIINGVIIVHSHVQWGDNESNPQDNPHSDSELILYNQLSAIFTTYLDTPAIDLKEPVRVVGVVPFFCDNLIALISELTPSNHLRAPPVA
>NZ_CP024595.1|WP_088442951.1|2291521_2292514_+|putative-sulfate-exporter-family-transporter
MNTDNPKSHISRIAYPAIIVFLILTLLGSLVERFHSFTSWLTPPVALLMGLAYALIFGSTHRRANKLGSKVLLQYSVVGLGFGMNLGESLASGRDGMMFTIISVFGTLLLGWFIGRKILQMNRNTSALISAGTAICGGSAIAAVGPILKAEEHEMSVALGTVFLLNAVALFIFPSIGHWLALDQQQFGTWAAIAIHDTSSVVGAGSAYGEEALRVATTIKLTRALWIVPLTLVFSFVYKTKGAKRFPVPLFILFFIGAIILNTYLLEAYFPEVGRFVASLARKGLTLSLFFIGASLTKEVIASVGVRALLQGLFLWILISVGSLAFILLI
>NZ_CP024595.1|WP_021664493.1|2292657_2294001_+|deoxyguanosinetriphosphate-triphosphohydrolase-family-protein
MTMMQWERLLSDKRVGMEHYHQPKQSAQPWERTDFERDYDRMVFSSPFRRLQNKAQVFPLAGNIFVHNRLTHSLEVSCVGRSLGNNITRGLKARYGELPWESGAISAIVSAACLAHDMGNPPFGHSGERAISAYFREGKGRVWEDAVRKEGGRWEDFLHFEGNANAFRLLTHQFEGRRKGGFALTYSTVASIVKYPYSSEMAGKAGKFGFFATEEDTFLMIAEELGMLCRNEHPVKYARYPLVYLVEAADDICYQIMDIEDAYKLRILTYAETENLFLAFCPEEELGHIRGVLDHITDANEQIAYLRSRVISLLVESCTRVFLDHEDEILSGTFSGTLIGAMEPRLKEAYGACARMAYSKIYVARDVVDVELAGHQIFGALIDKMMQALTNPDHAYSRTLLSRVSTQYNIREESLYGKIQCTLDYISGMTDIYALDLYRKITGMNLR
>NZ_CP024595.1|WP_097616251.1|2294061_2294778_+|4-hydroxy-tetrahydrodipicolinate-reductase
MKIVLIGYGKMGHVIERIACSRGHEVVLTIDAGEEDRFDSIAFRSADVAIEFTRPDAAYANCSRCMDKSVPVVCGTTGWTERLPELEERCRREGKTLFWASNFSIGVNLFFSLSRMFARLMSRHDQYRPHLTEIHHVHKLDAPSGTAITLAEGLIAESPSLDAWRLTETPEENELPITSIREDEVPGTHSISYTSEVDRLTICHEAFGREGFALGAVLAAEYAATHKGFLTMNDLISL
>NZ_CP024595.1|WP_004583651.1|2294793_2296191_+|signal-peptidase-I
MTFHWKDLTPWRRIKGVAITILYLLFCIWAGPFWLIFLPLIVDYYFFHIIKWGWYKNIRNKTLRIICSWVADIIYCVVAVTFIFAFLFQNFAIPTSSLEKTLLIGDYLFVSKLSYGPRSPMTPLGVPLTHNTMPLTGGKSFSDKPLLPYKRLKGFGHVKEGDLVVFNFPAGDTVAVKQPNPDYYMWKKLVGREELWSNPDFYGEIVYRPVDRRDHYVKRCVGMPGQELSIRNNQIYIDGKEQRNPRNMQLNYLVRMSREMSVDLIDELGISYDDVRAASSEELKASVGSNLIDSASNQPQIIYHLPLTQGMLDKLQAEPSFVKAVEEPTPIGPLYPLEYETGWTRDNYGPIVIPAKGMTVRLTPLNLALYSRCIRNFEGNKLVQKADGTVLINGRTADSYTFKMDYYFMMGDNRHNSADSRYWGFVPEDHIVGKPVFIWLSLNKDKSLFGGKIRFGRMMRTVNAD
>NZ_CP024595.1|WP_012458630.1|2296180_2296807_+|signal-peptidase-I
MQIKSRYRNRIFFIGLPAVVLLSAVLIRLFLVTTYRVRSDAMLPTYRSGKLLWINRIASPDRGDVLVIKYRQDGEADSRFYLARLIGLPGDTLFLSKGGVVANRQKLKLPTSLLPREPYKIIVPRNDRTYRLTPLSLLACRRAIEEECSSNISFRRGKLYRDGAETAFFHFRRNYYWILADNPASGPDSRHLGIVPEESIVGVVMNAN

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Crispr_ID: NZ_CP024595_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP024595_6

2316825-2317017

TypeIII

Consensus_repeat	Method
GTACTCACTATACATACACAGTCCGTAAGGCTATTAAGACAC	PILER-CR
CTCACTATACATACACAGTCCGTAAGGCTATTAAGAC	CRISPRCasFinder

2 spacers

cas2,cas1,cmr6gr7,cmr5gr11,cmr4gr7,cmr3gr5,cas10,cmr1gr7

The CRISPR arrays of NZ_CP024595_6

>merge|NZ_CP024595|6|2316825-2317017|PILER-CR,CRISPRCasFinder
GTACTCACTATACATACACAGTCCGTAAGGCTATTAAGACTACTTTTCGGCCAATTCTGTTGGGACGTTGTCCGTCCTCACTATACATACACAGTCCGTAAGGCTATTAAGACACATACATGTAAACATATGTTTCGATGCCATAGTCTGATAGCTCACTATACATACACAGTCCGTAAGGCTATTAAGACAC

>NZ_CP024595|6|5|2316825-2317017|PILER-CR
GTACTCACTATACATACACAGTCCGTAAGGCTATTAAGACTA	CTTTTCGGCCAATTCTGTTGGGACGTTGTCC
GTCCTCACTATACATACACAGTCCGTAAGGCTATTAAGACAC	ATACATGTAAACATATGTTTCGATGCCATAGTCTGA
TAGCTCACTATACATACACAGTCCGTAAGGCTATTAAGACAC

>NZ_CP024595|6|6|2316828-2317015|CRISPRCasFinder
CTCACTATACATACACAGTCCGTAAGGCTATTAAGAC	TACTTTTCGGCCAATTCTGTTGGGACGTTGTCCGTC
CTCACTATACATACACAGTCCGTAAGGCTATTAAGAC	ACATACATGTAAACATATGTTTCGATGCCATAGTCTGATAG
CTCACTATACATACACAGTCCGTAAGGCTATTAAGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP024595.1\|WP_021677507.1\|2324652_2325651_+\|mechanosensitive-ion-channel	unknown	unknown	gnl\|CDD\|182386
NZ_CP024595.1\|WP_099779625.1\|2304927_2306511_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779633.1\|2311081_2311783_+\|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	gnl\|CDD\|187813
NZ_CP024595.1\|WP_099779631.1\|2309889_2311068_+\|type-III-B-CRISPR-module-associated-protein-Cmr3	cmr3gr5	cd09656_cmr3gr5_CAS-III-B	gnl\|CDD\|273855
NZ_CP024595.1\|WP_099779635.1\|2312219_2312966_+\|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	cd09661_cmr6gr7_CAS-III-B	gnl\|CDD\|187792
NZ_CP024595.1\|WP_143733548.1\|2317277_2317385_-\|DUF1661-domain-containing-protein	unknown	unknown	gnl\|CDD\|285160
NZ_CP024595.1\|WP_012458609.1\|2317353_2317524_+\|DUF1661-domain-containing-protein	unknown	unknown	gnl\|CDD\|285160
NZ_CP024595.1\|WP_099779634.1\|2311779_2312223_+\|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	mkCas0098_cmr5gr11_CAS-III-B	unknown
NZ_CP024595.1\|WP_099779644.1\|2323663_2324551_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP024595.1\|WP_021679467.1\|2325611_2327408_-\|chloride-channel-protein	unknown	unknown	gnl\|CDD\|238233
NZ_CP024595.1\|WP_099779627.1\|2306776_2308225_+\|hypothetical-protein	cmr1gr7	mkCas0086_cmr1gr7_CAS-III-B	unknown
NZ_CP024595.1\|WP_099779639.1\|2318593_2320600_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP024595.1\|WP_099779640.1\|2320962_2322018_-\|hemagglutinin	unknown	unknown	unknown
NZ_CP024595.1\|WP_039424499.1\|2306512_2306770_+\|hypothetical-protein	cmr1gr7	mkCas0102_cmr1gr7_CAS-III-B	unknown
NZ_CP024595.1\|WP_099779629.1\|2308217_2309888_+\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl\|CDD\|274208
NZ_CP024595.1\|WP_099779642.1\|2322665_2323568_+\|T9SS-type-A-sorting-domain-containing-protein	unknown	unknown	gnl\|CDD\|275036
NZ_CP024595.1\|WP_099779637.1\|2313021_2316117_+\|CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187766
NZ_CP024595.1\|WP_005874926.1\|2316136_2316427_+\|CRISPR-associated-endonuclease-Cas2	cas2	pfam09827_cas2_CAS-I:CAS-II:CAS-III	gnl\|CDD\|187856
NZ_CP024595.1\|WP_021677506.1\|2327404_2328811_-\|sugar-transferase	unknown	unknown	gnl\|CDD\|274398
NZ_CP024595.1\|WP_026292128.1\|2317973_2318564_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP024595.1\|WP_099779631.1\|2309889_2311068_+\|type-III-B-CRISPR-module-associated-protein-Cmr3	gnl\|CDD\|273855	TIGR01888, Hypothetical_protein_SSO1730, CRISPR type III-B/RAMP module-associated protein Cmr3. CRISPR is a term for Clustered Regularly Interspaced Short Palidromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR associated) proteins. This highly divergent family is found in at least ten different archaeal and bacterial species as part of the CRISPR RAMP modulue but is not a member of the RAMP superfamily itself. A typical example is TM1793 from Thermotoga maritima.	1.56519e-80
NZ_CP024595.1\|WP_021677507.1\|2324652_2325651_+\|mechanosensitive-ion-channel	gnl\|CDD\|182386	PRK10334, PRK10334, small-conductance mechanosensitive channel MscS.	1.97356e-59
NZ_CP024595.1\|WP_099779633.1\|2311081_2311783_+\|type-III-B-CRISPR-module-RAMP-protein-Cmr4	gnl\|CDD\|187813	cd09682, Cmr4_III-B, CRISPR/Cas system-associated RAMP superfamily protein Cmr4. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; RAMP superfamily protein; This protein is a subunit of Cmr complex.	1.38943e-85
NZ_CP024595.1\|WP_012458609.1\|2317353_2317524_+\|DUF1661-domain-containing-protein	gnl\|CDD\|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	8.77199e-09
NZ_CP024595.1\|WP_099779644.1\|2323663_2324551_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|274350	TIGR02917, TPR_domain_protein, putative PEP-CTERM system TPR-repeat lipoprotein. This protein family occurs in strictly within a subset of Gram-negative bacterial species with the proposed PEP-CTERM/exosortase system, analogous to the LPXTG/sortase system common in Gram-positive bacteria. This protein occurs in a species if and only if a transmembrane histidine kinase (TIGR02916) and a DNA-binding response regulator (TIGR02915) also occur. The present of tetratricopeptide repeats (TPR) suggests protein-protein interaction, possibly for the regulation of PEP-CTERM protein expression, since many PEP-CTERM proteins in these genomes are preceded by a proposed DNA binding site for the response regulator.	9.42348e-15
NZ_CP024595.1\|WP_021679467.1\|2325611_2327408_-\|chloride-channel-protein	gnl\|CDD\|238233	cd00400, Voltage_gated_ClC, CLC voltage-gated chloride channel. The ClC chloride channels catalyse the selective flow of Cl- ions across cell membranes, thereby regulating electrical excitation in skeletal muscle and the flow of salt and water across epithelial barriers. This domain is found in the halogen ions (Cl-, Br- and I-) transport proteins of the ClC family. The ClC channels are found in all three kingdoms of life and perform a variety of functions including cellular excitability regulation, cell volume regulation, membrane potential stabilization, acidification of intracellular organelles, signal transduction, transepithelial transport in animals, and the extreme acid resistance response in eubacteria. They lack any structural or sequence similarity to other known ion channels and exhibit unique properties of ion permeation and gating. Unlike cation-selective ion channels, which form oligomers containing a single pore along the axis of symmetry, the ClC channels form two-pore homodimers with one pore per subunit without axial symmetry. Although lacking the typical voltage-sensor found in cation channels, all studied ClC channels are gated (opened and closed) by transmembrane voltage. The gating is conferred by the permeating ion itself, acting as the gating charge. In addition, eukaryotic and some prokaryotic ClC channels have two additional C-terminal CBS (cystathionine beta synthase) domains of putative regulatory function.	1.4503e-101
NZ_CP024595.1\|WP_143733548.1\|2317277_2317385_-\|DUF1661-domain-containing-protein	gnl\|CDD\|285160	pfam07877, DUF1661, Protein of unknown function (DUF1661). This is a family containing bacterial proteins of unknown function. Many of the proteins in this family are hypothetical.	0.000634986
NZ_CP024595.1\|WP_005874926.1\|2316136_2316427_+\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	8.2336e-16
NZ_CP024595.1\|WP_099779635.1\|2312219_2312966_+\|type-III-B-CRISPR-module-RAMP-protein-Cmr6	gnl\|CDD\|187792	cd09661, Cmr6_III-B, CRISPR/Cas system-associated RAMP superfamily protein Cmr6. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; RAMP superfamily protein; This protein is a subunit of Cmr complex.	1.17006e-64
NZ_CP024595.1\|WP_099779637.1\|2313021_2316117_+\|CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|187766	cd09634, Cas1_I-II-III, CRISPR/Cas system-associated protein Cas1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas1 is the most universal CRISPR system protein thought to be involved in spacer integration; Cas1 is metal-dependent deoxyribonuclease, also binds RNA; Shown to possess a unique fold consisting of a N-terminal beta-strand domain and a C-terminal alpha-helical domain.	6.63589e-69
NZ_CP024595.1\|WP_099779629.1\|2308217_2309888_+\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	gnl\|CDD\|274208	TIGR02577, thermophile-specific_DNA_repair_system, CRISPR-associated protein Cas10/Cmr2, subtype III-B. This model represent a Crm2 family of the CRISPR-associated RAMP module, a set of six genes recurring found together in prokaryotic genomes. This gene cluster is found only in species with CRISPR repeats, usually near the repeats themselves. Because most of the six (but not this family) contain RAMP domains, and because its appearance in a genome appears to depend on other CRISPR-associated Cas genes, the set is designated the CRISPR RAMP module. This protein, typified by TM1794 from Thermotoga maritima, is designated Crm2, for CRISPR RAMP Module protein 2.	6.97071e-80
NZ_CP024595.1\|WP_021677506.1\|2327404_2328811_-\|sugar-transferase	gnl\|CDD\|274398	TIGR03025, EPS_sugtrans, exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase. Members of this family are generally found near other genes involved in the biosynthesis of a variety of exopolysaccharides. These proteins consist of two fused domains, an N-terminal hydrophobic domain of generally low conservation and a highly conserved C-terminal sugar transferase domain (pfam02397). Characterized and partially characterized members of this subfamily include Salmonella WbaP (originally RfbP), E. coli WcaJ, Methylobacillus EpsB, Xanthomonas GumD, Vibrio CpsA, Erwinia AmsG, Group B Streptococcus CpsE (originally CpsD), and Streptococcus suis Cps2E. Each of these is believed to act in transferring the sugar from, for instance, UDP-glucose or UDP-galactose, to a lipid carrier such as undecaprenyl phosphate as the first (priming) step in the synthesis of an oligosaccharide "block". This function is encoded in the C-terminal domain. The liposaccharide is believed to be subsequently transferred through a "flippase" function from the cytoplasmic to the periplasmic face of the inner membrane by the N-terminal domain. Certain closely related transferase enzymes, such as Sinorhizobium ExoY and Lactococcus EpsD, lack the N-terminal domain and are not found by this model.	3.91045e-129
NZ_CP024595.1\|WP_099779642.1\|2322665_2323568_+\|T9SS-type-A-sorting-domain-containing-protein	gnl\|CDD\|275036	TIGR04183, hypothetical_protein, Por secretion system C-terminal sorting domain. Species that include Porphyromonas gingivalis, Fibrobacter succinogenes, Flavobacterium johnsoniae, Cytophaga hutchinsonii, Gramella forsetii, Prevotella intermedia, and Salinibacter ruber average twenty or more copies of a C-terminal domain, represented by this model, associated with sorting to the outer membrane and covalent modification.	6.99598e-10

>NZ_CP024595.1|WP_005874926.1|2316136_2316427_+|CRISPR-associated-endonuclease-Cas2
MNDKKLLVAYDISSNRRRRKVARILEQCGIRINKSVFICSLRELTMDKLVEAVTSQTAKRDKVFFLPLCQHCYTAAWMSGHPTLPKSRRKRKSIVV
>NZ_CP024595.1|WP_099779637.1|2313021_2316117_+|CRISPR-associated-endonuclease-Cas1
MPLSTDSLPIFLSDFTAYHFSVRFRAERAIAFERKWYFMPRFALGNALKNSEQYAYLYGQIFKPQEEDTDESKGPGNTSRLIIRADKPSRKSLEAGEALDLYITVVTRDPLLVGDFLSFLPEWQAYNFFRENDLTYDSYRLYNPTTEKYESGLRVEDAALTVDFFSRQAIRWGEILSVRFLSPASIKVDQILSAEIPYSRLMNRLSRRLYELYTQYLSWGETSVERYIFPDHDGLIYSQISMPRKATIKENRQYDMSGILGQLFYRVPYDPVAALMLSMAHWVHIGNHTIVGNGQIESTPGNDTLYRKWLSSLAADRDLPMAEAERQDLLEALRICSYIPQPYHSVNIPKGDGSYRQLHIPSAVDLHLQRSLAGILYPITESLSIAQSYAYRKGKGAVAAVRRVQHLLDSLDENHTVVRCDIDNFFDSIPVPSLLQKVQRTTEDPFLTRMLSLWMKSGVVDRKQQYARASSGVPQGSPLAPLLSNLYLEDTDRYIAGHITTEFIRYADDLLLFLPEKVDPLNALQDLSEHLKYRKGLKLNRDFVVSSIKSSFSFLGITFCADGSRSMSRDKKEGLKRKITLALHRDTENFSALSETIHGMEQYYRKLLEKVDIEAIDEVAATVYATYIASLPTSEARKSAKDNLLRLGFLSSETAKQTLREAMRQTVVSSADNFPIKKESEILREQQKRQLQEREEIFDLVVTEPGAFIGISRNHVLVRKYGKTICKRPAAQIEQISIISDGVSLSSNVTKYCRKKNIRVIFYNATGQAYASLNGMNTILPSVMEAQMRLSEEKKQEFILALIKNKVRNQGKLLRYYHKYYRHDKELKEPLSNAIAELKQLEGIPIAEGSSLADFRQHAMLHEARCAQVYWRAFALLVHRSGHEFEGREHKGAEGLVNQMLNYGYAILRSYVMKTIVLWQLNPNIGILHSTQDNKPALCFDLMEQYRAFVVDRSILALLAKGEDVGQNNKGLLDMPTRSRIISKINERWFATEYYRSGEKLFSDIMKLQTKDVRAFCCGKVKRIKFYTPKW
>NZ_CP024595.1|WP_099779635.1|2312219_2312966_+|type-III-B-CRISPR-module-RAMP-protein-Cmr6
MNFGHWYYREYFDTINLDSEGIVTNFSTFNKGKNDKLIKGAALPPYDKENDIEDVTSFELKTCYPGLLCGVGYHHEINNPKNEPKEDDAPEVYNLGMYFDYTSGLPVIPGSSIKGMLRSAIEEWDFLADYKPNNGVTREEIIKTVFEGKGLSIYDRDIFLDAIPIKADNKLFGEDYITHHPNPLQNPNPVRFLRVNPGVTYQFRFILRNNDNGLKADFKEDLFKAIICTFGLGAKTNVGYGQFVEPEK
>NZ_CP024595.1|WP_099779634.1|2311779_2312223_+|type-III-B-CRISPR-module-associated-protein-Cmr5
MNKKTIQDLIPKAMQAIEGVGIVGKDKKFEKVHEGYINALGPTIIQSGLLPTLIFYNKDKRELWLKALYYMEIISNDIDPTAIIQLIIKEGDSESRQEKTLKELEGKAKEWERKILEYAVALKLALRTFVAEEAETSNTKQQEGGAQ
>NZ_CP024595.1|WP_099779633.1|2311081_2311783_+|type-III-B-CRISPR-module-RAMP-protein-Cmr4
MKTAAYMIHCLTNMHVGKGDATYEVVDKCVQRDVTTGMPCIYSSSLKGALRQFFSKQGFAELNYVFGKDQNRDKKNNSNEKNEEEHSVGNFTFFQANLLAYPVQTTQEGATYILKTNKTLQDPIKELANLLSAPSNIEEMLPEGTEKDLSNEDLEQLPVIARNQLDNGKSENLWYEEVVPAESRFVFFVSYDDEEIFAKFDKIIQEGVIQIGANGSIGYGFCKIANVTNPFKK
>NZ_CP024595.1|WP_099779631.1|2309889_2311068_+|type-III-B-CRISPR-module-associated-protein-Cmr3
MSTYLIKLTPLDKFFFGQKKTFGDDNANYFVYSSLFPQQTALLGLLRYQLLQIAGEEIFKDNKIQDEHKAGELIGKQSFSPFVEEELQFGIIESLSSVFIIDKMNEDEHFLPVGRRFQKENEKAPYNLLHLSCQAGCPPIFGEYKPKKGLASCWLSSKSHTLLNEEDFFTKDERIGIRKDYEGATNDDAFFCQRYYRFKNFKEVEGEKTKVCKQPPVREHDFCFAVLLETHRDIKHEELNKRIVYLGGERQPFLMDLMEVSEETFKLTIESSTLTSDEKHYTVVLLSDAMIESKLLSEVRFASTEVKDFACLLTHVGTRKFYNKENKRQTQYLTESATALSVQKELYARGSVFYFDTKEQADQFCEDLKKVPNFHTIGYNHTIVIKPTKTKE
>NZ_CP024595.1|WP_099779629.1|2308217_2309888_+|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MSNEIYTAITIGPICKTLDKARSVKSFWTASYLFSWIMRELLERLPKEERPEGSFEVLSPHRDGKDVSEETSKKVGLFPDRLFAKGELEEKELKRIKREIFGELAEKFKNAFQDEKDDIARKIDTERDPKRKRELEEIKSRYSNAASKSEDIRKYLENYLSISSITVELSSDCSILEQLNKYLDTQELFNKASSHTDEDYMELFIEASKNSFLEDYSKENTSSSGSNKDLKESSTKKRAFPSTSEIAVSGWEQDPPKDENGEVEYSKLTSKKGFRNCYKYLAVIKADGDGFGTYIKNLNVNKENELTRFTKSFFEFSVEVANELIQKTKAIPVYIGGDDLFLFAPVLEGNVEKDVFNLIKEIDDLFIQKEIGEGLSMSYGVSIFYYKSPMSEAIDIADSMLRKAKEEKEEKEKKKDTVAISIQKHSGQKIEFLLPCKHSTDKCKQETGLYKKATELIRAFKEDDSMLNSLIYWIENMYETIFTDEVTLYQERINAVFDNFFDEEIHKENEVFFDLLKKFIHSMHHSEDTPRKLKDKKKLLHGILRYCQFVTAKKEK
>NZ_CP024595.1|WP_099779627.1|2306776_2308225_+|hypothetical-protein
MYKLEFELEQHTPIIHFQARDAGATLRASEVKPKLDKFVLTQIGKGFVNDPKANEEEYYKEGKKHLQNKDAEARRVYEEEKKKGNKDAKLELCLIPGQEGALNYKLSFKLSPDAKVQYFLPMSSNPKEIDKLKSLAQEKLGVQEVEMLPLTSYFANEDKAKSEPNIKHGDTPDQIKNKKRIFEENWQKVQLATFVNTPVEGVIRFQNAGLREEVNNLITNFFMLHNFGARQSKGFGSFIISLRDGKEEEDYFDTGCACYGYSFYIPAKTLEEALRKINYFYRSLRSGFNEYRGKNEIFYAKSGMHFYATKHNFEWDKKSIKGMLFDRDKDLEGKMKKEELFAFRDLLGLSSNERWQSYKTTITKECRNKKGEKFDRIKSPIQFKPICYSKYDYIVFFDLFPEKSGIPQLKGGKVVVKSSRHKGAVLELKIQEDIDLYNVFNEIFSELNFESQVGEYDSLTDAKEIFETMKDIYEQLNKNCHE
>NZ_CP024595.1|WP_039424499.1|2306512_2306770_+|hypothetical-protein
MEIETLILLSLAVAGFTTIIVVAIVWYSKFKIRKEELRDKTLVELERERTKDLNKWQSFSESLLATNKEIIEVYCKNNIKQKQEA
>NZ_CP024595.1|WP_099779625.1|2304927_2306511_+|hypothetical-protein
MGAETYSRHIFIFPFQWDYIEKRGYASYNERTDIKKFDKLFSAVSPLKRQYFEIGASEERYNEYTYFHPFARRALFGTKENPSVYHYELSDTQGSYNISVKIDGVSTTYSLQLEKIAVSVFDTGVGTVAYFLRNEKHTSFEDILRINDSGRRIYPQYMAKGNRLKAKDSFLADRIYGSLGVLDFDDDFRQFEEDISHTNIFLPPDHIRQVFGYNKMDRTEDDGCQKFVFHQESERKDIIRISPVMDDRMFFITYYHSPYYAKKLRSKPKNFRRKREYNIYEEGRFGDLWFRYIFGDGGDKTVANTSVQREDVRRTTYARWSGSGTLFGLTKDSLVGISGWELMGDHITTMYYQMATLSLVQRSTILRFSNEIASITQLILDKKTKRKTEKQVKELYGNYIRFLNETYFREVTPQIQGIEMYDMLQSNMNIEKDAKALDEEMGELFNYTTLEEQGVLNKTANLYLPITLLVGFLGINTFVEKGCITRFFNIGDPCPSTWGLLCGDIITLIVFAICLYFPIRHYFKYRK
>NZ_CP024595.1|WP_143733548.1|2317277_2317385_-|DUF1661-domain-containing-protein
MAREFFTSRTKTKKFPRHVFQSIDSLLQRVRYPLL
>NZ_CP024595.1|WP_012458609.1|2317353_2317524_+|DUF1661-domain-containing-protein
MVREVKNSRATAKKFSRRFSRKHAPQSEHFRSVNFGEADLSAKESSVVFGGGDRLV
>NZ_CP024595.1|WP_026292128.1|2317973_2318564_+|hypothetical-protein
MKRTLVFLFLTAVLALRAEAQSAPEQSETKDFIFSPQKEMVYVAIGYPAGIGLPSLDNYNVEGASASFAVGYERGVKQLAEGLLLSIYAELDWAAFRSVSDKRSLPFSDDSAQNRFRFLAGAGVHKRLNPNIELYARGAVGASFFPENNGSSSRELKGGFNVSLRVGLSCSLRDNFAVFIDTGTSDIVRGGLALMW
>NZ_CP024595.1|WP_099779639.1|2318593_2320600_+|hypothetical-protein
MKPLLTVVCAIILLSLPLGGQTVVPEWDEYIAEQIESGALGEDEGAEFLERWMVQKQRPLDINTLTREDLEQFPFLDEFQIRRFLLYRHAHPEGFDSIWVLNEIAGWDRRTCLLLWPMLTVQKRSEPAVGSFREILSYARHDVSVHTDAILQRQEGYRPDSRHPYRGDPWGGGLRWSYAMGNRFSLGLTASKDRGEPAFDKRRKGFDSYSAHFFMEGKGAVRAVALGDYRIGMGYGLLVNQASFMGMAYAYPRGGTTLRRAFTYAEDNFMRGAATALAQGRWTLTAFYSHKGVDATVTEDGAIKAIYHTGLHRTDAEIARRNAATMTTAGTSVCYTDDRLRLTFNLLHLHWGGLRLLRAVGTQGIASLTDLERFSLVSADYSYLFGQGETELFGEFAGAANGAVGTINGLRYTHPVGGSYMLVGRYIPADYWSYYRGAFARYSRPGNEWGVMGRAAWELPSDRTVRAFADYYGSFVPRFGRKEKTEALYWMFEGEKRLSALSWSCRIRGTADKRYRRSLAVRLRGRYTFDERWRLMASLQWSRSNSFDGQQQVWQAPTGGKSFALRADYSGGKLLRVCSVDAVAFDTDSFADRLYEAVHNPRHHYSSAFFYGRGVRLGVFVRIAPLPQVEVESRIDHLLRRDTDTIGSAGELIRGQARTHLFMTVRYR
>NZ_CP024595.1|WP_099779640.1|2320962_2322018_-|hemagglutinin
MTVENLRLQRLQNLEHYRFAKNVLTLCRTANIAKLNPKLPELEKAIEMEDLALNPPVANELTPQVIALDEERDRAYQALMSRVRSYAFDEDSQLRNAAARIEDVAARYGNVIRMNYDKETAAIENFLTDLKGENIRPLVTKLGVTALVDRLEKNNKAFADFFLRRLSTDQRGKYDVKALRAETDRTLVAVVRRMDSIDDMEPSPEIRALIELYNRLVANRRALLARRASYGEAAVEKRRAEIAEMLRPLLARIVDEKKTAVFAGRTLGTGKNRHYLITFVAENGDEEDRWYRIDGEQLVYVPEDELPKPKKKKKPASSTDTPSEPPVLPNPSQEGGSSSGGGEQGSTGGGL
>NZ_CP024595.1|WP_099779642.1|2322665_2323568_+|T9SS-type-A-sorting-domain-containing-protein
MAFAQVPKGNDKSKDEHILTWALPEELVIDNDSIVATYNSFLTPFNGMTMACASFFDVQDLLPYVGYTINRIDFHPTADEKNYEQVAASKFYICIWGNKEQTEVLYEQALPTIHKEDLSFGYGVDGEEDYYDEPMYLAELETPFVIPAGKALYIGCRVETQEGHAVGFGLDDGPAMKGKGDLVGSYLPGAAPMPFVPLSDIPARSMDANFFIYSRISLGSGTHDILQHRMKVYPNPATTELHVEALSAWVGEQAAVYDMRGRRVSARTVDSEKLCIDIASLPVGVYMLRIGSYSAKFEKR
>NZ_CP024595.1|WP_099779644.1|2323663_2324551_-|tetratricopeptide-repeat-protein
MTDRFLHILRLSALCLLFSALLPPLFGQPTTARQDSLPADYTRLIDRSFEALGQGNLELAEQALRQAIKAYPDLPSGYALMNNLGAIQQRQGKPEEALLTYSAALQKLPDDKLLRTNRAMLLTEMGRTDEAIFDYNELLRAEPDNEIFHYGRAMLYLAKGMYGDAESDLEEILRINDSSLKARLGIALVATMKGEYDKAERLYNYVIDKLPKNAAAYEGRARLFLNKGMKGYALRDINKAFEYATPPAASLFVLRGEINAAIGDKKAAAEDYAAAESRGYSKESLDVLRAALRKQ
>NZ_CP024595.1|WP_021677507.1|2324652_2325651_+|mechanosensitive-ion-channel
MGLKIFFPLQNLSVDTTKVNKIAEVVSPEALKQIKDIKPSQWTELLTQWGGKALSFGIKVLIALVAFYLGKLLLNALVKWLDRIMVRRSFEPAARTFLRSFANIGGFVLLIVIIISTLGFQPVSLAALLASVGVAVGMGLSGQLQNLAGGLIVLLTKPFKVGDYIVSNNVEGVVDGVTLFHTTVMTFENKYIFIPNGLLSSNVIINYSRMAVRRNEWIIGIEYNEDFDRVKTLLLRLIDEEPRIIKEPLPTVVLKELADSSVRVMARAWCATDDLWNVYWDINERIYSEFNRQGIAFPFPQLTIHGSAAGQERRGKSTEAQSPENVSTNTSL
>NZ_CP024595.1|WP_021679467.1|2325611_2327408_-|chloride-channel-protein
MKDKETSRYGWFLHFLLWRERHINERLFLIILSLIIGILSAFAAVLLKNTIHIIQHFAFDRIRETSYLYLIFPVVGILITWLFVRYVVRDDIGHGVTKILFAISQRKSRIKPHNMWSSLAASSITIGFGGSVGAESPIVLTGAAIGSNLGRLFRMEQKTLMLLVGCGAAGAISGIFKAPITGLVFVIEVLLLDLTMSSVLPLLISSVSAAAVSYIITGQGAMFSFTLNDPFSMDRIPYALLLGVFCGLVSFYFSKVMFVFESKLKNFPHYRERYLISAFILCGLIFLFPPLYGEGYDTINALLGGQYSSLMDGSLFEPYSNSYWVLFVFLGFIIITKVFASVATNSGGGCGGLFAPSLFMGALSGFIFAYALNFFPFIEVYLPQKNFALLGMAGVMAAVMHAPLTGIFLIAELTGGYNLFLPLMLVSTSSYATIRLFMPHSIYSLRLAQKGKLLTHQKDKAVLTLMTLDAVIEKDFEPVRPDMTLGDVVHVFGISHRNVFPVLDENNLLMGLVLLDNIRNIMFRPELYERFKVSRFMVSPPAKIVNTMSMETIMRIFDDTKAWNLPVIDEQGCYLGFVSKSKIFNSYREVLVETFSGD
>NZ_CP024595.1|WP_021677506.1|2327404_2328811_-|sugar-transferase
MTRMQLHRLRYLLADVFGIVASYLSYNTLRYLTEEQERIYSTLSEYLFNAKSLWVGILYLLFWLSLFALSGYYNKPIAKSRISELLTTVASVLVGSVVVFLLLVVDDIVHDTALYLRLFFMMVATVLPWVYFPRLWVTTFGIKERKKTKGYHRVLLIGSGTIAEETASWLKSVNDMATTRLHFVPPTMREGFEQSLKSFATLVAEAVQESKPHQIILAVDCPDASFISLLLYQLYPFHMPVCVPMRSMLFAGAKVNVQGMKGEPMVDMTATNMSECAKSIKWFADRLFSLLMLILLIPVYAVIAVLVKRSSRGPVFFGQERIGLHGRPFTIYKFRTMYLDAEKDGPSLSFDGDSRVTPIGRILRKYRMDELPQFWNVLRGDMSFVGPRPERAFYIRQLVERAPYYYLLHNVRPGITSWGMVRYGYASTPDEMLERLQYDFLYYENMSLRLDIEVLLYTCQTIFKGLGK

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	NC_013940	Deferribacter desulfuricans SSM1 megaplasmid pDF308, complete sequence	98837-98866	5	0.833
NZ_CP024595_1	1.5\|265111\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265111-265140	30	NZ_CP029358	Azospirillum sp. CFH 70021 plasmid unnamed3	79334-79363	5	0.833
NZ_CP024595_1	1.13\|265112\|29\|NZ_CP024595\|CRT	265112-265140	29	NZ_CP029358	Azospirillum sp. CFH 70021 plasmid unnamed3	79334-79362	5	0.828
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	NZ_CP013709	Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence	184572-184601	6	0.8
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	MN694740	Marine virus AFVG_250M752, complete genome	53063-53092	6	0.8
NZ_CP024595_1	1.12\|265046\|29\|NZ_CP024595\|CRT	265046-265074	29	NZ_CP013709	Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence	184573-184601	6	0.793
NZ_CP024595_1	1.13\|265112\|29\|NZ_CP024595\|CRT	265112-265140	29	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	330761-330789	6	0.793
NZ_CP024595_3	3.4\|1082641\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082641-1082670	30	NC_009425	Enterobacter sp. 638 plasmid pENTE01, complete sequence	87615-87644	6	0.8
NZ_CP024595_3	3.4\|1082641\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082641-1082670	30	NC_009425	Enterobacter sp. 638 plasmid pENTE01, complete sequence	98752-98781	6	0.8
NZ_CP024595_1	1.5\|265111\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265111-265140	30	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	330760-330789	7	0.767
NZ_CP024595_1	1.12\|265046\|29\|NZ_CP024595\|CRT	265046-265074	29	NC_022877	Bacillus thuringiensis YBT-1518 plasmid pBMB0232, complete sequence	1861-1889	7	0.759
NZ_CP024595_1	1.12\|265046\|29\|NZ_CP024595\|CRT	265046-265074	29	MN694792	Marine virus AFVG_250M662, complete genome	14576-14604	7	0.759
NZ_CP024595_1	1.12\|265046\|29\|NZ_CP024595\|CRT	265046-265074	29	MN694757	Marine virus AFVG_250M663, complete genome	14581-14609	7	0.759
NZ_CP024595_1	1.12\|265046\|29\|NZ_CP024595\|CRT	265046-265074	29	MN692977	Marine virus AFVG_117M37, complete genome	35649-35677	7	0.759
NZ_CP024595_1	1.13\|265112\|29\|NZ_CP024595\|CRT	265112-265140	29	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	1772992-1773020	7	0.759
NZ_CP024595_1	1.13\|265112\|29\|NZ_CP024595\|CRT	265112-265140	29	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1854314-1854342	7	0.759
NZ_CP024595_3	3.7\|1082839\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082839-1082868	30	NZ_CP022346	Bacillus thuringiensis strain c25 plasmid unnamed1, complete sequence	236691-236720	7	0.767
NZ_CP024595_3	3.8\|1082905\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082905-1082934	30	NZ_LR699557	Paraburkholderia sp. Msb3 isolate PDMSB31 plasmid pIII	29894-29923	7	0.767
NZ_CP024595_3	3.8\|1082905\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082905-1082934	30	NC_005262	Burkholderia cepacia phage Bcep22, complete genome	58185-58214	7	0.767
NZ_CP024595_5	5.147\|2281136\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2281136-2281171	36	NZ_CP012185	Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence	250401-250436	7	0.806
NZ_CP024595_5	5.147\|2281136\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2281136-2281171	36	NZ_CP012182	Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence	173785-173820	7	0.806
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	NC_022877	Bacillus thuringiensis YBT-1518 plasmid pBMB0232, complete sequence	1860-1889	8	0.733
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	MN694792	Marine virus AFVG_250M662, complete genome	14576-14605	8	0.733
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	MN694757	Marine virus AFVG_250M663, complete genome	14581-14610	8	0.733
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	MN692977	Marine virus AFVG_117M37, complete genome	35648-35677	8	0.733
NZ_CP024595_1	1.4\|265045\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265045-265074	30	MN694471	Marine virus AFVG_250M232, complete genome	22994-23023	8	0.733
NZ_CP024595_1	1.5\|265111\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265111-265140	30	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	1772991-1773020	8	0.733
NZ_CP024595_1	1.5\|265111\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder	265111-265140	30	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	1854314-1854343	8	0.733
NZ_CP024595_1	1.12\|265046\|29\|NZ_CP024595\|CRT	265046-265074	29	MN694471	Marine virus AFVG_250M232, complete genome	22995-23023	8	0.724
NZ_CP024595_3	3.4\|1082641\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082641-1082670	30	MN850603	Escherichia phage pinkbiff, complete genome	47287-47316	8	0.733
NZ_CP024595_3	3.4\|1082641\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082641-1082670	30	KX377933	Escherichia phage vB_EcoM_Alf5, complete genome	9652-9681	8	0.733
NZ_CP024595_3	3.5\|1082707\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082707-1082736	30	NC_018683	Sinorhizobium meliloti Rm41 plasmid pSYMA, complete sequence	82295-82324	8	0.733
NZ_CP024595_3	3.5\|1082707\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082707-1082736	30	NZ_CP021809	Sinorhizobium meliloti strain Rm41 plasmid psymA, complete sequence	545216-545245	8	0.733
NZ_CP024595_3	3.6\|1082773\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082773-1082802	30	CP011075	Brevibacillus laterosporus strain B9 plasmid unnamed1, complete sequence	230104-230133	8	0.733
NZ_CP024595_3	3.6\|1082773\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082773-1082802	30	NZ_CP016589	Bacillus thuringiensis strain KNU-07 plasmid pBTKNU07-01, complete sequence	324143-324172	8	0.733
NZ_CP024595_3	3.6\|1082773\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082773-1082802	30	MN855975	Siphoviridae sp. isolate 45, complete genome	11967-11996	8	0.733
NZ_CP024595_5	5.1\|2271511\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2271511-2271545	35	NC_018689	Bacillus thuringiensis MC28 plasmid pMC429, complete sequence	295406-295440	8	0.771
NZ_CP024595_5	5.42\|2274216\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2274216-2274251	36	MF360958	Salicola phage SCTP-2, complete genome	22501-22536	8	0.778
NZ_CP024595_5	5.102\|2278165\|35\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2278165-2278199	35	MH622943	Myoviridae sp. isolate ctbc_4, complete genome	196060-196094	8	0.771
NZ_CP024595_3	3.9\|1082971\|30\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	1082971-1083000	30	NZ_LR134418	Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9	397066-397095	9	0.7
NZ_CP024595_5	5.62\|2275532\|34\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2275532-2275565	34	NZ_CP018188	Streptococcus salivarius strain ICDC2 plasmid, complete sequence	144038-144071	9	0.735
NZ_CP024595_5	5.65\|2275727\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2275727-2275762	36	NZ_CP015884	Enterococcus faecalis strain sorialis plasmid Efsorialis-p1, complete sequence	65552-65587	9	0.75
NZ_CP024595_5	5.69\|2275992\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2275992-2276027	36	NC_027396	Streptococcus phage SpSL1, complete genome	14319-14354	9	0.75
NZ_CP024595_5	5.3\|2271644\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2271644-2271678	35	NZ_CP017574	Bacillus thuringiensis strain SCG04-02 plasmid PSCG364, complete sequence	147057-147091	10	0.714
NZ_CP024595_5	5.3\|2271644\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2271644-2271678	35	NZ_CP009595	Bacillus cereus strain 3a plasmid pBFC_3, complete sequence	311583-311617	10	0.714
NZ_CP024595_5	5.3\|2271644\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2271644-2271678	35	NZ_CP009606	Bacillus cereus strain S2-8 plasmid pBFR_2, complete sequence	177818-177852	10	0.714
NZ_CP024595_5	5.3\|2271644\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2271644-2271678	35	NZ_CP053994	Bacillus cereus strain FDAARGOS_780 plasmid unnamed1, complete sequence	251589-251623	10	0.714
NZ_CP024595_5	5.3\|2271644\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2271644-2271678	35	NZ_CP053992	Bacillus cereus strain FDAARGOS_781 plasmid unnamed2, complete sequence	234605-234639	10	0.714
NZ_CP024595_5	5.10\|2272108\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2272108-2272142	35	NZ_CP017574	Bacillus thuringiensis strain SCG04-02 plasmid PSCG364, complete sequence	147057-147091	10	0.714
NZ_CP024595_5	5.10\|2272108\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2272108-2272142	35	NZ_CP009595	Bacillus cereus strain 3a plasmid pBFC_3, complete sequence	311583-311617	10	0.714
NZ_CP024595_5	5.10\|2272108\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2272108-2272142	35	NZ_CP009606	Bacillus cereus strain S2-8 plasmid pBFR_2, complete sequence	177818-177852	10	0.714
NZ_CP024595_5	5.10\|2272108\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2272108-2272142	35	NZ_CP053994	Bacillus cereus strain FDAARGOS_780 plasmid unnamed1, complete sequence	251589-251623	10	0.714
NZ_CP024595_5	5.10\|2272108\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2272108-2272142	35	NZ_CP053992	Bacillus cereus strain FDAARGOS_781 plasmid unnamed2, complete sequence	234605-234639	10	0.714
NZ_CP024595_5	5.30\|2273424\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2273424-2273459	36	MN032679	Leviviridae sp. isolate H1_Rhizo_25_scaffold_979 hypothetical protein (H1Rhizo25979_000001), hypothetical protein (H1Rhizo25979_000002), and RNA-dependent RNA polymerase (H1Rhizo25979_000003) genes, complete cds	3580-3611	10	0.722
NZ_CP024595_5	5.109\|2278629\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2278629-2278664	36	AP013384	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C111A-MedDCM-OCT-S34-C44	3952-3987	10	0.722
NZ_CP024595_5	5.109\|2278629\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2278629-2278664	36	AP013579	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C111A-MedDCM-OCT-S25-C41, * SEQUENCING IN PROGRESS *	23170-23205	10	0.722
NZ_CP024595_5	5.126\|2279753\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2279753-2279788	36	AP013384	Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C111A-MedDCM-OCT-S34-C44	3952-3987	10	0.722
NZ_CP024595_5	5.126\|2279753\|36\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2279753-2279788	36	AP013579	Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C111A-MedDCM-OCT-S25-C41, * SEQUENCING IN PROGRESS *	23170-23205	10	0.722
NZ_CP024595_5	5.151\|2281400\|35\|NZ_CP024595\|CRISPRCasFinder,CRT,PILER-CR	2281400-2281434	35	NC_015712	Clostridium perfringens plasmid pCPPB-1, complete sequence	20191-20225	10	0.714
NZ_CP024595_5	5.3\|2271644\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2271644-2271678	35	NZ_CP009691	Bacillus mycoides strain ATCC 6462 plasmid pBMX_1, complete sequence	286873-286907	11	0.686
NZ_CP024595_5	5.10\|2272108\|35\|NZ_CP024595\|PILER-CR,CRISPRCasFinder,CRT	2272108-2272142	35	NZ_CP009691	Bacillus mycoides strain ATCC 6462 plasmid pBMX_1, complete sequence	286873-286907	11	0.686

1. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to NC_013940 (Deferribacter desulfuricans SSM1 megaplasmid pDF308, complete sequence) position: , mismatch: 5, identity: 0.833

attttctttaactgtatctaatatattagt-	CRISPR spacer
atttgctttaacagtatctaata-atgactg	Protospacer
**** ******* ********** ** * *

2. spacer 1.5|265111|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to NZ_CP029358 (Azospirillum sp. CFH 70021 plasmid unnamed3) position: , mismatch: 5, identity: 0.833

tgcagacgcaggcgggtatgcccgatcttg-	CRISPR spacer
tgcagacgcaggcggatatg-ccgctgtcgg	Protospacer
***************.**** *** * *.*

3. spacer 1.13|265112|29|NZ_CP024595|CRT matches to NZ_CP029358 (Azospirillum sp. CFH 70021 plasmid unnamed3) position: , mismatch: 5, identity: 0.828

gcagacgcaggcgggtatgcccgatcttg-	CRISPR spacer
gcagacgcaggcggatatg-ccgctgtcgg	Protospacer
**************.**** *** * *.*

4. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to NZ_CP013709 (Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence) position: , mismatch: 6, identity: 0.8

attttctttaactgtatctaatatattagt	CRISPR spacer
aataacgttaactgtagcttatatattagt	Protospacer
* *  * ********* ** **********

5. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to MN694740 (Marine virus AFVG_250M752, complete genome) position: , mismatch: 6, identity: 0.8

attttctttaactgtatctaatatattagt	CRISPR spacer
attttctttatctgtatctaaattttcagc	Protospacer
********** **********  * *.**.

6. spacer 1.12|265046|29|NZ_CP024595|CRT matches to NZ_CP013709 (Clostridium botulinum strain F634 plasmid pRSJ2_2, complete sequence) position: , mismatch: 6, identity: 0.793

ttttctttaactgtatctaatatattagt	CRISPR spacer
ataacgttaactgtagcttatatattagt	Protospacer
 *  * ********* ** **********

7. spacer 1.13|265112|29|NZ_CP024595|CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 6, identity: 0.793

gcagacgcaggcgggtatgcccgatcttg	CRISPR spacer
gcgcgtggaggcgggtctgcccgatcttg	Protospacer
**. ..* ******** ************

8. spacer 3.4|1082641|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NC_009425 (Enterobacter sp. 638 plasmid pENTE01, complete sequence) position: , mismatch: 6, identity: 0.8

tcatcaggtggtgatgatgtctggattgcc	CRISPR spacer
ttttcaggagctgatgatgtctggatttgc	Protospacer
*. ***** * ****************  *

9. spacer 3.4|1082641|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NC_009425 (Enterobacter sp. 638 plasmid pENTE01, complete sequence) position: , mismatch: 6, identity: 0.8

tcatcaggtggtgatgatgtctggattgcc	CRISPR spacer
ttttcaggagctgatgatgtctggatttgc	Protospacer
*. ***** * ****************  *

10. spacer 1.5|265111|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 7, identity: 0.767

tgcagacgcaggcgggtatgcccgatcttg	CRISPR spacer
cgcgcgtggaggcgggtctgcccgatcttg	Protospacer
.**. ..* ******** ************

11. spacer 1.12|265046|29|NZ_CP024595|CRT matches to NC_022877 (Bacillus thuringiensis YBT-1518 plasmid pBMB0232, complete sequence) position: , mismatch: 7, identity: 0.759

ttttctttaactgtatctaatatattagt	CRISPR spacer
gtttctttaaatgtatctaatctactcaa	Protospacer
 ********* ********** **.* .

12. spacer 1.12|265046|29|NZ_CP024595|CRT matches to MN694792 (Marine virus AFVG_250M662, complete genome) position: , mismatch: 7, identity: 0.759

ttttctttaactgtatctaatatattagt	CRISPR spacer
cctcttttaactgcatctattatattagg	Protospacer
..*..********.***** ********

13. spacer 1.12|265046|29|NZ_CP024595|CRT matches to MN694757 (Marine virus AFVG_250M663, complete genome) position: , mismatch: 7, identity: 0.759

ttttctttaactgtatctaatatattagt	CRISPR spacer
cctcttttaactgcatctattatattagg	Protospacer
..*..********.***** ********

14. spacer 1.12|265046|29|NZ_CP024595|CRT matches to MN692977 (Marine virus AFVG_117M37, complete genome) position: , mismatch: 7, identity: 0.759

ttttctttaactgtatctaatatattagt	CRISPR spacer
tattctttaactttatctaatatccattt	Protospacer
* ********** ********** .   *

15. spacer 1.13|265112|29|NZ_CP024595|CRT matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 7, identity: 0.759

gcagacgcaggcgggtatgcccgatcttg	CRISPR spacer
ccagtcgcaggcgggtgtgcccgagaacg	Protospacer
 *** ***********.*******   .*

16. spacer 1.13|265112|29|NZ_CP024595|CRT matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 7, identity: 0.759

gcagacgcaggcgggtatgcccgatcttg	CRISPR spacer
ccagtcgcaggcgggtgtgcccgagaacg	Protospacer
 *** ***********.*******   .*

17. spacer 3.7|1082839|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP022346 (Bacillus thuringiensis strain c25 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

agtttgaatatagacggttttttatcatta	CRISPR spacer
tttatgaaaataaacggttttttatcagaa	Protospacer
  * **** ***.**************  *

18. spacer 3.8|1082905|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR699557 (Paraburkholderia sp. Msb3 isolate PDMSB31 plasmid pIII) position: , mismatch: 7, identity: 0.767

ctaacccaaaggcataagagttggcgattt	CRISPR spacer
cccggataaaggcgtaagagttggcgattt	Protospacer
*. .  .******.****************

19. spacer 3.8|1082905|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NC_005262 (Burkholderia cepacia phage Bcep22, complete genome) position: , mismatch: 7, identity: 0.767

ctaacccaaaggcataagagttggcgattt	CRISPR spacer
cctctcccaaggcataagggttggcgatct	Protospacer
*.  .** **********.*********.*

20. spacer 5.147|2281136|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012185 (Pseudonocardia sp. EC080619-01 plasmid pBCI1-2, complete sequence) position: , mismatch: 7, identity: 0.806

---gcatcgcgaccatcgatgacgaacgccgccttcgta	CRISPR spacer
ggcacatcg---ccatcgttgacgaacgccgccatcgtg	Protospacer
   .*****   ****** ************** ****.

21. spacer 5.147|2281136|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012182 (Pseudonocardia sp. EC080610-09 plasmid pBCI2-1, complete sequence) position: , mismatch: 7, identity: 0.806

---gcatcgcgaccatcgatgacgaacgccgccttcgta	CRISPR spacer
ggcacatcg---ccatcgttgacgaacgccgccatcgtg	Protospacer
   .*****   ****** ************** ****.

22. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to NC_022877 (Bacillus thuringiensis YBT-1518 plasmid pBMB0232, complete sequence) position: , mismatch: 8, identity: 0.733

attttctttaactgtatctaatatattagt	CRISPR spacer
tgtttctttaaatgtatctaatctactcaa	Protospacer
  ********* ********** **.* .

23. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to MN694792 (Marine virus AFVG_250M662, complete genome) position: , mismatch: 8, identity: 0.733

attttctttaactgtatctaatatattagt	CRISPR spacer
tcctcttttaactgcatctattatattagg	Protospacer
 ..*..********.***** ********

24. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to MN694757 (Marine virus AFVG_250M663, complete genome) position: , mismatch: 8, identity: 0.733

attttctttaactgtatctaatatattagt	CRISPR spacer
tcctcttttaactgcatctattatattagg	Protospacer
 ..*..********.***** ********

25. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to MN692977 (Marine virus AFVG_117M37, complete genome) position: , mismatch: 8, identity: 0.733

attttctttaactgtatctaatatattagt	CRISPR spacer
gtattctttaactttatctaatatccattt	Protospacer
.* ********** ********** .   *

26. spacer 1.4|265045|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to MN694471 (Marine virus AFVG_250M232, complete genome) position: , mismatch: 8, identity: 0.733

attttctttaactgtatctaatatattagt	CRISPR spacer
agtttctttaattgtatctaataatcccat	Protospacer
* *********.***********  .. .*

27. spacer 1.5|265111|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 8, identity: 0.733

tgcagacgcaggcgggtatgcccgatcttg	CRISPR spacer
gccagtcgcaggcgggtgtgcccgagaacg	Protospacer
  *** ***********.*******   .*

28. spacer 1.5|265111|30|NZ_CP024595|PILER-CR,CRISPRCasFinder matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 8, identity: 0.733

tgcagacgcaggcgggtatgcccgatcttg	CRISPR spacer
gccagtcgcaggcgggtgtgcccgagaacg	Protospacer
  *** ***********.*******   .*

29. spacer 1.12|265046|29|NZ_CP024595|CRT matches to MN694471 (Marine virus AFVG_250M232, complete genome) position: , mismatch: 8, identity: 0.724

ttttctttaactgtatctaatatattagt	CRISPR spacer
gtttctttaattgtatctaataatcccat	Protospacer
 *********.***********  .. .*

30. spacer 3.4|1082641|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to MN850603 (Escherichia phage pinkbiff, complete genome) position: , mismatch: 8, identity: 0.733

tcatcaggtggtgatgatgtctggattgcc	CRISPR spacer
tcatcaggtgctgatgatgtcagaacatta	Protospacer
********** ********** *.*.  .

31. spacer 3.4|1082641|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to KX377933 (Escherichia phage vB_EcoM_Alf5, complete genome) position: , mismatch: 8, identity: 0.733

tcatcaggtggtgatgatgtctggattgcc	CRISPR spacer
tcatcaggtgctgatgatgtcagaacatta	Protospacer
********** ********** *.*.  .

32. spacer 3.5|1082707|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NC_018683 (Sinorhizobium meliloti Rm41 plasmid pSYMA, complete sequence) position: , mismatch: 8, identity: 0.733

aagggcgaaactgtactcgacatctgcagc	CRISPR spacer
gatctcgaaactgtactctacatctacaat	Protospacer
.*   ************* ******.**..

33. spacer 3.5|1082707|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP021809 (Sinorhizobium meliloti strain Rm41 plasmid psymA, complete sequence) position: , mismatch: 8, identity: 0.733

aagggcgaaactgtactcgacatctgcagc	CRISPR spacer
gatctcgaaactgtactctacatctacaat	Protospacer
.*   ************* ******.**..

34. spacer 3.6|1082773|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to CP011075 (Brevibacillus laterosporus strain B9 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.733

ttttttgttttcatactatgtatgtttttg	CRISPR spacer
ttttttgttttcctactatgcattcgtcat	Protospacer
************ *******.** . *.

35. spacer 3.6|1082773|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP016589 (Bacillus thuringiensis strain KNU-07 plasmid pBTKNU07-01, complete sequence) position: , mismatch: 8, identity: 0.733

ttttttgttttcatactatgtatgtttttg	CRISPR spacer
gtttttattttcatattatgtatgctaaga	Protospacer
 *****.********.********.*   .

36. spacer 3.6|1082773|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to MN855975 (Siphoviridae sp. isolate 45, complete genome) position: , mismatch: 8, identity: 0.733

ttttttgttttcatactatgtatgtttttg	CRISPR spacer
ttttttgttttcataatatctatatacaaa	Protospacer
*************** *** ***.* .  .

37. spacer 5.1|2271511|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NC_018689 (Bacillus thuringiensis MC28 plasmid pMC429, complete sequence) position: , mismatch: 8, identity: 0.771

aatttgggaattacgatgaagaaaagcattttttc	CRISPR spacer
tgttttggaatttcgatgaagaaaagcacctctta	Protospacer
 .*** ****** ***************..*.**

38. spacer 5.42|2274216|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to MF360958 (Salicola phage SCTP-2, complete genome) position: , mismatch: 8, identity: 0.778

-atgtagtaattaaatctattataaatcatatttctt	CRISPR spacer
aacattg-aattaaatatattataattcatatttgtc	Protospacer
 *..* * ******** ******** ******** *.

39. spacer 5.102|2278165|35|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to MH622943 (Myoviridae sp. isolate ctbc_4, complete genome) position: , mismatch: 8, identity: 0.771

ctgaaaact--caaatagtttgatgatttattgcata	CRISPR spacer
--taaagttgataaaaagtttgatgatttattacata	Protospacer
   ***..*  .*** ****************.****

40. spacer 3.9|1082971|30|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR134418 (Legionella adelaidensis strain NCTC12735 genome assembly, plasmid: 9) position: , mismatch: 9, identity: 0.7

gataaatactctaagtcttcagcctcctct	CRISPR spacer
gataaaaactctaagtcttcaaacgaaagc	Protospacer
****** **************. *     .

41. spacer 5.62|2275532|34|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018188 (Streptococcus salivarius strain ICDC2 plasmid, complete sequence) position: , mismatch: 9, identity: 0.735

acgaaatgatcaaaaaggagtttatccaccgcac	CRISPR spacer
acgaaacgatcaaaaaggagcttatttatgccga	Protospacer
******.*************.****..*.  *.

42. spacer 5.65|2275727|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP015884 (Enterococcus faecalis strain sorialis plasmid Efsorialis-p1, complete sequence) position: , mismatch: 9, identity: 0.75

tttattacgttatagaaatcatcttcatctgctaac	CRISPR spacer
tctaaattattatagaaatcatcttgatctgttaag	Protospacer
*.**   ..**************** *****.***

43. spacer 5.69|2275992|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to NC_027396 (Streptococcus phage SpSL1, complete genome) position: , mismatch: 9, identity: 0.75

tctcctctacatcctcaggagaaggagaccatgctg	CRISPR spacer
ggccatcaacatcctcaggagcaggagaccagtcag	Protospacer
  .* ** ************* *********  * *

44. spacer 5.3|2271644|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP017574 (Bacillus thuringiensis strain SCG04-02 plasmid PSCG364, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

45. spacer 5.3|2271644|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009595 (Bacillus cereus strain 3a plasmid pBFC_3, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

46. spacer 5.3|2271644|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009606 (Bacillus cereus strain S2-8 plasmid pBFR_2, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

47. spacer 5.3|2271644|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP053994 (Bacillus cereus strain FDAARGOS_780 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

48. spacer 5.3|2271644|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP053992 (Bacillus cereus strain FDAARGOS_781 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

49. spacer 5.10|2272108|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP017574 (Bacillus thuringiensis strain SCG04-02 plasmid PSCG364, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

50. spacer 5.10|2272108|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009595 (Bacillus cereus strain 3a plasmid pBFC_3, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

51. spacer 5.10|2272108|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009606 (Bacillus cereus strain S2-8 plasmid pBFR_2, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

52. spacer 5.10|2272108|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP053994 (Bacillus cereus strain FDAARGOS_780 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

53. spacer 5.10|2272108|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP053992 (Bacillus cereus strain FDAARGOS_781 plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.714

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaattattcaaaaaggagcaattcgtaagtttcca	Protospacer
. ..*.  *******.*.***************.*

54. spacer 5.30|2273424|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to MN032679 (Leviviridae sp. isolate H1_Rhizo_25_scaffold_979 hypothetical protein (H1Rhizo25979_000001), hypothetical protein (H1Rhizo25979_000002), and RNA-dependent RNA polymerase (H1Rhizo25979_000003) genes, complete cds) position: , mismatch: 10, identity: 0.722

gagggcgcagatagggcttagaaccctatctgcttt	CRISPR spacer
aggaacgcacatagggcttagaaccctatcta----	Protospacer
..*..**** *********************.

55. spacer 5.109|2278629|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to AP013384 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C111A-MedDCM-OCT-S34-C44) position: , mismatch: 10, identity: 0.722

tcacgaacaagacgcagctgataagcgcaatcaact	CRISPR spacer
aattgaccaagacgcagctgataaacgcaagaaggt	Protospacer
   .** *****************.*****  *. *

56. spacer 5.109|2278629|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to AP013579 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C111A-MedDCM-OCT-S25-C41, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 10, identity: 0.722

tcacgaacaagacgcagctgataagcgcaatcaact	CRISPR spacer
aattgaccaagacgcagctgataaacgcaagaaggt	Protospacer
   .** *****************.*****  *. *

57. spacer 5.126|2279753|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to AP013384 (Uncultured Mediterranean phage uvMED DNA, complete genome, group G15, isolate: uvMED-CGR-C111A-MedDCM-OCT-S34-C44) position: , mismatch: 10, identity: 0.722

tcacgaacaagacgcagctgataagcgcaatcaact	CRISPR spacer
aattgaccaagacgcagctgataaacgcaagaaggt	Protospacer
   .** *****************.*****  *. *

58. spacer 5.126|2279753|36|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to AP013579 (Uncultured Mediterranean phage uvMED isolate uvMED-CGF-C111A-MedDCM-OCT-S25-C41, *** SEQUENCING IN PROGRESS ***) position: , mismatch: 10, identity: 0.722

tcacgaacaagacgcagctgataagcgcaatcaact	CRISPR spacer
aattgaccaagacgcagctgataaacgcaagaaggt	Protospacer
   .** *****************.*****  *. *

59. spacer 5.151|2281400|35|NZ_CP024595|CRISPRCasFinder,CRT,PILER-CR matches to NC_015712 (Clostridium perfringens plasmid pCPPB-1, complete sequence) position: , mismatch: 10, identity: 0.714

agaataatcaatggaagaattagaatggatttttc	CRISPR spacer
agaatattcaatagaagaattagaagaagcatata	Protospacer
****** *****.************ .... * *

60. spacer 5.3|2271644|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009691 (Bacillus mycoides strain ATCC 6462 plasmid pBMX_1, complete sequence) position: , mismatch: 11, identity: 0.686

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaataattcaaaaaggagcaattcgtaagtttcca	Protospacer
. .. .  *******.*.***************.*

61. spacer 5.10|2272108|35|NZ_CP024595|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP009691 (Bacillus mycoides strain ATCC 6462 plasmid pBMX_1, complete sequence) position: , mismatch: 11, identity: 0.686

gtgctgaacaaaaagaaacaattcgtaagtttcta	CRISPR spacer
aaataattcaaaaaggagcaattcgtaagtttcca	Protospacer
. .. .  *******.*.***************.*

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

1473001 : 1524967

Streptococcus_virus(20.0%)

tRNA,protease,transposase

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

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_099779389.1\|1473001_1473916_-\|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA
WP_077492586.1\|1473899_1474616_-\|protease	rhomboid family intramembrane serine protease	NA	NA	NA	NA
WP_077492588.1\|1474642_1477498_-	LPS-assembly protein LptD	NA	NA	NA	NA
WP_099779390.1\|1477990_1478527_-	pyridoxamine 5'-phosphate oxidase family protein	NA	NA	NA	NA
WP_099779391.1\|1478789_1479755_+	cation transporter	NA	NA	NA	NA
WP_021664252.1\|1479751_1480270_-	hypothetical protein	NA	NA	NA	NA
WP_077492498.1\|1480359_1482045_-	putative transporter	NA	NA	NA	NA
WP_023846932.1\|1483950_1486554_+	TonB-dependent receptor plug domain-containing protein	NA	NA	NA	NA
WP_013816585.1\|1486989_1487931_+	2-nitropropane dioxygenase	NA	NA	NA	NA
WP_077492502.1\|1487927_1488155_+	cysteine-rich CWC family protein	NA	NA	NA	NA
WP_099779394.1\|1488223_1489870_+	fumarate hydratase	NA	NA	NA	NA
WP_099779395.1\|1489991_1491800_+	DNA polymerase III subunit gamma/tau	A0A1U9WR94	Streptococcus_virus	6.1e-46	39.1
WP_099779176.1\|1492086_1493459_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	2.0e-09	24.8
WP_010956309.1\|1493751_1493922_-	4Fe-4S dicluster domain-containing protein	NA	NA	NA	NA
WP_005873462.1\|1494257_1495790_-	D-alanyl-D-alanine carboxypeptidase/D-alanyl-D-alanine-endopeptidase	NA	NA	NA	NA
WP_061156921.1\|1496014_1497685_-	peptidylarginine deiminase PPAD	NA	NA	NA	NA
WP_099779396.1\|1498879_1501411_-	T9SS type A sorting domain-containing protein	NA	NA	NA	NA
WP_004585428.1\|1501549_1502035_-	6,7-dimethyl-8-ribityllumazine synthase	A0A2H4PQS3	Staphylococcus_phage	1.3e-27	42.9
WP_052912128.1\|1502126_1502813_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_021663568.1\|1502998_1503676_-	response regulator transcription factor	NA	NA	NA	NA
WP_099779397.1\|1503688_1505497_-	tetratricopeptide repeat-containing sensor histidine kinase	NA	NA	NA	NA
WP_013816575.1\|1505885_1506080_+	exodeoxyribonuclease VII small subunit	NA	NA	NA	NA
WP_021678656.1\|1506076_1506745_+	2-C-methyl-D-erythritol 4-phosphate cytidylyltransferase	NA	NA	NA	NA
WP_125026584.1\|1507585_1507660_-	DUF1661 domain-containing protein	NA	NA	NA	NA
WP_099779399.1\|1507947_1509036_-\|transposase	ISAs1 family transposase	NA	NA	NA	NA
WP_099779400.1\|1509295_1510831_+	hypothetical protein	NA	NA	NA	NA
WP_143738878.1\|1510886_1511114_+	hypothetical protein	NA	NA	NA	NA
WP_043894125.1\|1511211_1512051_+	GLPGLI family protein	NA	NA	NA	NA
WP_077492386.1\|1512029_1514642_+	hypothetical protein	NA	NA	NA	NA
WP_099779401.1\|1517841_1518927_+\|transposase	IS5 family transposase	A0A077K814	Ralstonia_phage	1.4e-18	27.5
WP_004585370.1\|1519356_1520184_+	FtsX-like permease family protein	NA	NA	NA	NA
WP_013815640.1\|1520230_1520458_+	DUF3098 domain-containing protein	NA	NA	NA	NA
WP_023847376.1\|1520565_1521408_+	undecaprenyl-diphosphate phosphatase	NA	NA	NA	NA
WP_013815638.1\|1521417_1522194_+\|tRNA	tRNA pseudouridine(55) synthase TruB	NA	NA	NA	NA
WP_012457606.1\|1522211_1523264_+\|tRNA	tRNA preQ1(34) S-adenosylmethionine ribosyltransferase-isomerase QueA	NA	NA	NA	NA
WP_004585365.1\|1523266_1523710_+	2-amino-4-hydroxy-6- hydroxymethyldihydropteridine diphosphokinase	NA	NA	NA	NA
WP_099779703.1\|1523722_1524967_+\|protease	collagenase-like protease	Q6DW11	Phage_TP	3.4e-16	24.4

Anti-CRISPR protein detection

Acr_ID: NZ_CP024595.1|WP_077491804.1|800845_801268_+|PcfK-like-protein

Click the colored protein region to show detailed information

Acr_ID: NZ_CP024595.1|WP_077085632.1|1305146_1305563_+|PcfK-like-protein

Click the colored protein region to show detailed information

Acr ID

Acr position

Acr size

Homology with known anti

Neighbor HTH/AcRanker

Neighbor Aca

In prophage

Protospacer in prophage

NZ_CP024595.1|WP_077491804.1|800845_801268_+|PcfK-like-protein

800845_801268_+

140 aa aa

hit_Aca_id	identity	query_coverage	hit_coverage
gnl\|BL_ORD_ID\|40	0.5319148936170213	1.0	0.9929078014184397

NZ_CP024595.1|WP_077085632.1|1305146_1305563_+|PcfK-like-protein

1305146_1305563_+

138 aa aa

hit_Aca_id	identity	query_coverage	hit_coverage
gnl\|BL_ORD_ID\|40	0.574468085106383	1	1.0

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP024595

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information