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_CP022203	Myxococcus macrosporus DSM 14697 chromosome, complete genome	19 crisprs	WYL,cas3,RT,Cas9_archaeal,DEDDh,PD-DExK,csa3,2OG_CAS,DinG,cas2,cas1,cas5,cas7,cas8b3,cas6,cmr6gr7,cmr5gr11,cmr4gr7,cmr3gr5,cas10,cmr1gr7	5	61	9	1

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP022203_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_1

31598-31803

Orphan

Consensus_repeat	Method
GGAGCCGCCGCTGGCCTCGGCGTCGA	CRT

3 spacers

The CRISPR arrays of NZ_CP022203_1

>merge|NZ_CP022203|1|31598-31803|CRT
GGAGCCGCCGCTGGCCTCGGTGTCCAGCGTCTTGACGCCCTTCACGTCCAGGGCGCGCACGGCGGAGCCGCCGCTGGCCTCGGCGTCGAACTCCGTCGCCCGGCCCGCCAGCGTCACCTGGGAGCCGCCGCTGGCCTCGGCCTCGACCTTGCGCGCGTCCACGCCGCGCACGGTGACGATGGCGCCGCCGCTGGCCTCGACGTCGA

>NZ_CP022203|1|1|31598-31803|CRT
GGAGCCGCCGCTGGCCTCGGTGTCCA	GCGTCTTGACGCCCTTCACGTCCAGGGCGCGCACGGC
GGAGCCGCCGCTGGCCTCGGCGTCGA	ACTCCGTCGCCCGGCCCGCCAGCGTCACCTG
GGAGCCGCCGCTGGCCTCGGCCTCGA	CCTTGCGCGCGTCCACGCCGCGCACGGTGACGAT
GGCGCCGCCGCTGGCCTCGACGTCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_013936809.1\|27964_28261_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095956555.1\|19947_21144_+\|type-II-toxin-antitoxin-system-HipA-family-toxin	unknown	unknown	gnl\|CDD\|377920
NZ_CP022203.1\|WP_095956559.1\|28792_30982_+\|tenascin-X	unknown	unknown	unknown
NZ_CP022203.1\|WP_095956565.1\|40116_42156_+\|PilZ-domain-containing-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095956562.1\|37430_38057_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013936811.1\|24845_25814_-\|glutathione-synthase	unknown	unknown	gnl\|CDD\|235371
NZ_CP022203.1\|WP_043709762.1\|28291_28588_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095956561.1\|35503_37399_+\|VacB/RNase-II-family-3'-5'-exoribonuclease	unknown	unknown	gnl\|CDD\|273947
NZ_CP022203.1\|WP_095956568.1\|43736_44894_+\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP022203.1\|WP_095956557.1\|22729_24625_-\|PHB-depolymerase-family-esterase	unknown	unknown	gnl\|CDD\|273828
NZ_CP022203.1\|WP_095956553.1\|18625_19408_-\|methyltransferase	unknown	unknown	gnl\|CDD\|226608
NZ_CP022203.1\|WP_095956563.1\|38066_38486_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_157757415.1\|43437_43647_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095956566.1\|42172_43129_-\|NYN-domain-containing-protein	unknown	unknown	gnl\|CDD\|350237
NZ_CP022203.1\|WP_095956569.1\|45240_45831_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP022203.1\|WP_095956564.1\|39339_39834_-\|YkgJ-family-cysteine-cluster-protein	unknown	unknown	gnl\|CDD\|308985
NZ_CP022203.1\|WP_095956554.1\|19565_19907_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|213767
NZ_CP022203.1\|WP_095956556.1\|21396_22707_+\|type-II-toxin-antitoxin-system-HipA-family-toxin-YjjJ	unknown	unknown	gnl\|CDD\|236623
NZ_CP022203.1\|WP_095956558.1\|25892_27599_-\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP022203.1\|WP_095956560.1\|32285_35243_-\|protein-kinase	unknown	unknown	gnl\|CDD\|270916

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095956566.1\|42172_43129_-\|NYN-domain-containing-protein	gnl\|CDD\|350237	cd11297, PIN_LabA-like_N_1, uncharacterized subfamily of N-terminal LabA-like PIN domains. This N-terminal LabA-like PIN domain is found in a well conserved group of mainly bacterial proteins with no defined function, which contain a C-terminal LabA_like_C domain. LabA from Synechococcus elongatus PCC 7942, (which does not contain this C-terminal domain), has been shown to play a role in cyanobacterial circadian timing. The LabA-like C-terminal domains characteristic of this subfamily may be related to the LOTUS domain family (which also co-occurs with LabA-like N-terminal domains). The function of the N-terminal domain is unknown. The LabA-like PIN domain family also includes the N-terminal domain of limkain b1, a human autoantigen localized to a subset of ABCD3 and PXF marked peroxisomes. Other members are the LabA-like PIN domains of human ZNF451, uncharacterized Bacillus subtilis YqxD and Escherichia coli YaiI. Curiously, a gene labeled NicB from Pseudomonas putida S16, which is described as a putative NADH-dependent hydroxylase involved in the microbial degradation of nicotine also falls into the LabA-like PIN family. The PIN (PilT N terminus) domain belongs to a large nuclease superfamily. The structural properties of the PIN domain indicate its active center, consisting of three highly conserved catalytic residues which coordinate metal ions; in some members, additional metal coordinating residues can be found while some others lack several of these key catalytic residues. The PIN active site is geometrically similar in the active center of structure-specific 5' nucleases, PIN-domain ribonucleases of eukaryotic rRNA editing proteins, and bacterial toxins of toxin-antitoxin (TA) operons.	1.53311e-42
NZ_CP022203.1\|WP_095956555.1\|19947_21144_+\|type-II-toxin-antitoxin-system-HipA-family-toxin	gnl\|CDD\|377920	pfam07804, HipA_C, HipA-like C-terminal domain. The members of this family are similar to a region close to the C-terminus of the HipA protein expressed by various bacterial species. This protein is known to be involved in high-frequency persistence to the lethal effects of inhibition of either DNA or peptidoglycan synthesis. When expressed alone, it is toxic to bacterial cells, but it is usually tightly associated with HipB, and the HipA-HipB complex may be involved in autoregulation of the hip operon. The hip proteins may be involved in cell division control and may interact with cell division genes or their products.	8.35891e-51
NZ_CP022203.1\|WP_013936811.1\|24845_25814_-\|glutathione-synthase	gnl\|CDD\|235371	PRK05246, PRK05246, glutathione synthetase; Provisional.	5.82951e-140
NZ_CP022203.1\|WP_095956561.1\|35503_37399_+\|VacB/RNase-II-family-3'-5'-exoribonuclease	gnl\|CDD\|273947	TIGR02063, Ribonuclease_R, ribonuclease R. This family consists of an exoribonuclease, ribonuclease R, also called VacB. It is one of the eight exoribonucleases reported in E. coli and is broadly distributed throughout the bacteria. In E. coli, double mutants of this protein and polynucleotide phosphorylase are not viable. Scoring between trusted and noise cutoffs to the model are shorter, divergent forms from the Chlamydiae, and divergent forms from the Campylobacterales (including Helicobacter pylori) and Leptospira interrogans. [Transcription, Degradation of RNA].	3.42734e-147
NZ_CP022203.1\|WP_095956568.1\|43736_44894_+\|IS4-family-transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain 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. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	1.83958e-05
NZ_CP022203.1\|WP_095956557.1\|22729_24625_-\|PHB-depolymerase-family-esterase	gnl\|CDD\|273828	TIGR01840, poly3-hydroxybutyrate_depolymerase_A_precursor, esterase, PHB depolymerase family. This model describes a subfamily among lipases of the ab-hydrolase family. This subfamily includes bacterial depolymerases for poly(3-hydroxybutyrate) (PHB) and related polyhydroxyalkanoates (PHA), as well as acetyl xylan esterases, feruloyl esterases, and others from fungi. [Fatty acid and phospholipid metabolism, Degradation].	9.5318e-74
NZ_CP022203.1\|WP_095956553.1\|18625_19408_-\|methyltransferase	gnl\|CDD\|226608	COG4123, COG4123, Predicted O-methyltransferase [General function prediction only].	2.34729e-53
NZ_CP022203.1\|WP_095956569.1\|45240_45831_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	6.3527e-06
NZ_CP022203.1\|WP_095956564.1\|39339_39834_-\|YkgJ-family-cysteine-cluster-protein	gnl\|CDD\|308985	pfam03692, CxxCxxCC, Putative zinc- or iron-chelating domain. This family of proteins contains 8 conserved cysteines. It has in the past been annotated as being one of the complex of proteins of the flagellar Fli complex. However this was due to a mis-annotation of the original Salmonella LT2 Genbank entry of 'fliB'. With all its conserved cysteines it is possibly a domain that chelates iron or zinc ions.	0.000242829
NZ_CP022203.1\|WP_095956554.1\|19565_19907_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|213767	TIGR03070, couple_hipB, transcriptional regulator, y4mF family. Members of this family belong to a clade of helix-turn-helix DNA-binding proteins, among the larger family pfam01381 (HTH_3; Helix-turn-helix). Members are similar in sequence to the HipB protein of E. coli. Genes for members of the seed alignment for this protein family were found to be closely linked to genes encoding proteins related to HipA. The HibBA operon appears to have some features in common with toxin-antitoxin post-segregational killing systems. [Regulatory functions, DNA interactions].	3.19163e-05
NZ_CP022203.1\|WP_095956556.1\|21396_22707_+\|type-II-toxin-antitoxin-system-HipA-family-toxin-YjjJ	gnl\|CDD\|236623	PRK09775, PRK09775, type II toxin-antitoxin system HipA family toxin YjjJ.	0
NZ_CP022203.1\|WP_095956558.1\|25892_27599_-\|serine/threonine-protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.24304e-85
NZ_CP022203.1\|WP_095956560.1\|32285_35243_-\|protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	2.70365e-79

>NZ_CP022203.1|WP_095956559.1|28792_30982_+|tenascin-X
MAHAKRVAAVSGLWWVLVLGVAACRDAPSLSGAVGRLRLSAQRVDFPPAYPGTRREAEVRVVNGGRAPLDVTWTEVTPPFYLEAPLPAQVLVGEVPVRLRFAPEAEGTYEATLTGTASDGGQVRLVLAGEARPVPECFTPVTCATATFDLVAEACVESLLPDGTACDPGNACLTGATCQAGRCRGEERACDDGNACTTDVCHVLDGCQAVPAPPCAAAGPCLVGTCDPKRGCVMASAPDGTLCGGARDTCEDVDVCLDGACVKRDLPEGFPCAAASPCQAAGQCRGGRCARPEAQPLTVDWTYDAQAQGQQLQDLLVGPEGDVTLSGFYGTPVLDAAKSPVRASNPARRCMLWNDRLLCMDMPVDGTVSLLERTTGAPRWTFTLGDARPDFRDRTRTLFLARLAVMAPDRLAALFEAYPAEERSDTACRRYFLVVLDAFGHMVSARELTDPLLSECDHPHPYGLASDAVGDLYVAFGPTRNVGAPLASGAPTLLMAFSSDGVPRWRRTESQRAGELAVANGLLLPEWGLQALSTRDGTPVGASFPQQLGRVVATRDVVVPSAPGTTVNAGTAGSSSPPAATRLTGFRLPDLEPAWAYSLREGQHLATKELRLATWPGAAGLPPETLVLTHAVAADHPGLLVGVRARDGSEAFQCSLDYAPRTLPQLMELGPGALYLMEGATSCGECDPPFANSQPRFLRFRAPGLMPAREPWPGTFGGPGHGHHENTVR
>NZ_CP022203.1|WP_043709762.1|28291_28588_-|hypothetical-protein
MTSAASSSCVPSSSQAFTVLIPRGLQAAVEGLPAETRQELLAELFRLAALARQEESQLPPEFPYTLRLDVAGCQVSVELEPSRSRLTLVGLLRPQPLE
>NZ_CP022203.1|WP_013936809.1|27964_28261_-|hypothetical-protein
MSRRAGYAESWDLTYLVEQLRELIGHDLRLDEVLAEELEDVLGSLVQRNQRLRVLQRMVNAERAPDDLAALRGALEDMDRELLTRLPALLERLRLALP
>NZ_CP022203.1|WP_095956558.1|25892_27599_-|serine/threonine-protein-kinase
MPAEGFPIDFYRGERIGKYEVVTQLSVGGMAELFLGFTSGPGGFRKYVVIKRVLPDARDNAQFERMFLDEARITAAFNHPNIAQVFDLGREDDGLYLAMEFIAGQNLNQITGACLKRHDQLSLGFTLSVARDVCMALHYAHTYTAPSGAPSPVIHRDVAQKNIMVTYDGVVKLLDFGIAKAKDSLERTNVGTVKGTTGYMSPEQVRGEALDGRSDLFSVGVMMHELITGARLFAGRNERDEMMKILDAPVPWPSTVAPHVPEEVSKVVMRALERSREKRFATGRDMAKAIEAAAGRLLLDATDRAALMQELFAERMSATRVMLESADGTTNGVILASAKRALRGDDGPYLPERKDLPTPSNGVSGLPRKPSRKVPAAPAPRRAAAPDTPPAPESRSSNVVWGLVLLGILVGGGYAAWHLSKVLNETVEEEAASALRTLPRHDPNLPVYPVPGYDTPTPDAGTPEAPARALGAAVGGEEAADAPPKETASARPAARGRGKLTLVVLPEAEVFRGAKRLGRTPMFNLALPVGNHELTLKGPDGKKRLLMVPITAGETTRFKLKLGEIPER
>NZ_CP022203.1|WP_013936811.1|24845_25814_-|glutathione-synthase
MASLTIGFLMDPLESVRVDHDSTFALMLEAQQRGHQVRYFEQGWLRFNGTCAEARMRHVTVRREAGRHFDVLDEAPLPVSALDVLFMRKDPPVDAEFLHATQLVELCGTRPPPVFINEPAGIRDANEKLFSLRYPDLMPDTRVTSELPVLLDFIARNAAGTILKPVDGFAGKGILFLSATDRNARSAVDMLTRGGREAVMAQAYIPESRQGDKRILLVDGEPVGGVLRVPSDDDHRGNMAAGGVPQKAVLTPRDVEICERLKPELVKRGLRLVGIDVLGTYLTEVNVTSPTGLVEANHLDNVCVEARVLDVAERLAAERAAR
>NZ_CP022203.1|WP_095956557.1|22729_24625_-|PHB-depolymerase-family-esterase
MLKQRCSRSWPWSRSAGVPLAAWLYAGLVGCGGPVSEAPEPGAEVAEQPQRLLTQVTGFGSNPGNLQMFRHVPSGMPANAPLVVVLHGCTQRAASMEGSGWSAAADVYKFYAVYPQQQSGNNMTSCFNWFEPGDIARDRGEALSIKQMVDTMKATYSVDPSRVYVAGFSAGAYMVPALLAAYPDVFSAGAIHSGGPYRCAESMTAGFNCMSPGVNRAPAAWGDLVRGAYPGYAGPRPRVSIWHGTSDYTVNVMNLTEAMEQWTNVHGIDQTPDTVETVSNFPHKVYRDGAGNALVETWELTGMGHGVAMDAQFQFPGGTGTAACGAVGAYLNDVNLCSVYHQARFFGLLDGGGEPTGDTTPPTVNVTAPANGATVGGTVNVTADAADAVGVTRVEFLVDGEVVSTDSQAPYAFAWNSAAVGNGQHRLGARAFDAAGNQATDNDTVVTVSNTGSPAPVTAQFTSIAAEDGYLKANADGSAAALGFMTNLALGRGTDGKYNRSFLSFDTSGLPDGATVTRAFLTVTYSSGSGDPWSTPAGNTLVIDVKTGTFNAANTEAADWAGAAAASSVAGIERFSAGAKRSGDFSAAGLSAINKAGKTQLRLRFTQAQTATQYLFVRDGANAVLTVVYTP
>NZ_CP022203.1|WP_095956556.1|21396_22707_+|type-II-toxin-antitoxin-system-HipA-family-toxin-YjjJ
MATLEQLLAVLGRQVEVKGGELATQLRVSRPTVSRLLASAGPSVCRMGQGPATRYARARSIAALGEQIPLYRVGETGRPSEAGILYPLWNGGCWVAQAEGVGERFAGLPPFAADMSPQGYLGRGFASRHPELGLPPRITDWTEDHQLIALALRGDDCVGDRIIGAASLDRFLASPLRPATEAQYPELARSSMSSEAGSSAGGEQPKFTAYTEGRHVLVKFAANDDGAAAQRWRELLVCEGLALEAVRAAGIPAAATRSLRVEGYQFLEVERFDRIGERGRKALLSLKAIDNEYLGHEGKGSTWTSAAHYLQQSQSISDEDARRIRWLDTFGQLTGNTDRHFGNLSFFEEGPKRFKLAPAYDMLPMMFAPVGTTIVERAFEPRPPTSETLDVWSDAARHALAYWTRLLEAQELSQAFRARCAQCRDSLAALMQRTPV
>NZ_CP022203.1|WP_095956555.1|19947_21144_+|type-II-toxin-antitoxin-system-HipA-family-toxin
MEVVTCGRFQQQGEVGRFVYGRSYLANPRAVELEKFELPLRPGTFETARLGGIFGSLRDASPDAWGRRVIERQLERVALSEVDFLLNSPEDRAGALSFGTSPTPPAPVHRFNKVLRLDLLLEEARRVEQELPLSGVQVSDLVNPGSSMGGARPKNVVEDEEGLWVAKFPARGDRWNNAAVEGGMLRLARECGLKAAVSKRTHVAGQDVLLVRRFDRQRVDGGYHRHRMVSALTVLRADEHPQDRSKWSYILLADELKRWVGDPDEDLRELFSRMVFNALISNVDDHPRNHALIAAGTAWNLSPAYDLTPSPQASLERHLAMEVGSAQHRRATRLNLLSECGRFRLSKEAANHLIDTMKATVTARWRGAIKDCGGTDADVTAVERAFDSEGFEYTHYSV
>NZ_CP022203.1|WP_095956554.1|19565_19907_+|helix-turn-helix-domain-containing-protein
MPRQNLTSDTAPLAVVRAVERLGQNIARARIRRGLRQVDLAKKTGLALGTLKRIEEGSPTTGLSAYFTVLWALGLEQEFDNLAAPERDEEGKTLELARQPQRVRLKKGLDADF
>NZ_CP022203.1|WP_095956553.1|18625_19408_-|methyltransferase
MPEPTLPPGPGPDETLDSIGTAGVRVLQRRTGYRFTLDAVLLAHFAATEGAGTPGRMLELGAGSGVVSFLLVKQFGLGPVDALEFQPSVHARLTRAVALNACEAHVTPLLGDLRRIREHVPGGLYAHVVSNPPFRLADAGVRSPDDERAMSKSEVACDAQSVVAAARYALAPGGGVSLVYPAARVAEVLGLLAQAKLHPTALRFVHARVGAPATRFLVHALRDRDRGLAVRPPLIVHGEGPGGYTPEVAALMDPPLAERT
>NZ_CP022203.1|WP_095956560.1|32285_35243_-|protein-kinase
MGDGAFASIRLTVYIRRHSMSGNRLPLAQEARTLGKYEVLCRLSTGGMAEIFLASQRGLAGFHKLVVLKQILPDIRGEEEFVRMFLDEAKVTAAFNHPHIAQVYDLDIADGELFLSMEFVPGATLVEVARACRQANTPIPMGYSLMAVRDTAVALHYAHTFTDPLGRPSPVIHRDVAEKNIMVTYEGVTKLLDFGIAKSLARASRTAVGMVKGTSGYMSPEQIMGEPLDARSDLFSLGVVLHECLTGMRLFYAKQADAMMNAVLRCEVTPPSRTNKQVPPELDAIVLRALSRRREDRYASTLEFARAIERAVGPLIWHPEQSSELMLRLFSDRRDQTRQLLMSGQDETGDTTGVVNLARVMAMGVEPSELPTGGVTVQPPNRGPGAARSAAPAPTPRRATAASPDAGTVRKAVLQAPPGKRLTSRASPADARPPPPPPETMAPPPPPPDSGVQHMRTQPGMPAHPPEHTVRTQLPGTGRDVGSPPPAPAEAHPRQSARAATAEAQAVAREQTQVRAPRPPEPPPAPEEPRADATRSRASRTPEASPSVDDAPRPRSARTPEASPAVEESPRAEARSRASRTQDGLRAVPPSELPAPRVAAEDAPRARAPRTQDGLRAAPTPPPVERDLQTAMIRMPVPPPDAGEDTTLPVSAAPRRSVPVRRRSMSAEHTTLPVRVRDLHDEEDEESTVMGRGDGARATRSTHLRPPPRRGKAWVALTAVVGMLALGAAAVVLKLDGGVVSSRLEPLLGQGAPPDPQAGSGTRTPPAPGNADDNKRATGTDTPAPGNADGKQVATGTDTPAPGNADDNKRATVTNTPAPGNAGDTVAAGTDTPVDAPVKDRTASPASGGIASLEAAGDVAPAPLTDRAPVLDEAPPKEPRTFKRVRNSTQRSRMVTSSPRKAPSSSEDIPAGEPGFLTLVTEPRAQVFLGGQDLGKTPLFKVKLPAGQHTLKLVDATSKAHQVPVDIKPGETTSVRGPLSLLSDP
>NZ_CP022203.1|WP_095956561.1|35503_37399_+|VacB/RNase-II-family-3'-5'-exoribonuclease
MDTSVSPRTVTGRLDVHPRGFGFLTVQTPGSPEVLSAFVPPPDLNPYFAGDVVTATVTAGADGRWSASNLSLVERPRTQVYGEVVLRKGAPLLRVDREVANADWTLDTAGTQVQAGDAVVARIDEGKVVLLYRVEAGEDRSLERVIARHELRKDFPAEVVEEARSARAVPHAAGARRDLRSVPTVTVDAPSTRDIDDAISVLPAGPDGALRLLVSIADVGEYVKQGTALDAEARERATSVYLAGRVLPMLPEELSSHWLSLVQGEERLCLTVELRIDPQGRVTAADVYESIIRSWARLDYDEVAAFLDRGEVSAPMEPVREVMPWFRLAAARLAVARAARGGMEFARDEARFTFDQATGELSGLVSEKPTSAHAMIERFMVAANESIAGWLLARGLPGVYRVHEQPDPLRVADLNAFAETSGFAAGFGRELTPLALAAFDRQIAGAVAEPALRSVLRRSLGPSRYTVKPGPHFGLAAPLYLHFTSPIRRYADLAVHRTLKGYLQGRRDFVDEDPRVEALAAHINAKARASTRAENDRHRELEARWMAGHVGKQFPARVTRVRPFGLVAQLDGMLVEGVVPTDALTGGPFRPDARELSLVGRERTFTVGMPVTVKVTSTDEQLGRIELALAE
>NZ_CP022203.1|WP_095956562.1|37430_38057_+|hypothetical-protein
MSLRWARIALLLTACGGAGYRYAGRDIYFGPEGGQVWVRGPWPAIQPSRNVDDVIDQLCPIIMEMDGAREKEYGQEYCGVLYSLGDGVFHASYPSPIGEMQRIGPNKRKSCTSPRYVRDARGRAVGIADYHSHPWAPSPLTPEDRWEKNQRWLIRIQFDTDCHVMKLVPHSNEPRPGEVYLRKGRTWELIGIIKPEHKPLGIVTDVGG
>NZ_CP022203.1|WP_095956563.1|38066_38486_+|hypothetical-protein
MKCRALLLTVVLLPGCVLFQRPFRPEHAPKEEAAKLPYPLWLPSEGRVQVPANLAAAIGLAMDDMLPRDVKPPRDATPDDVCLHRRDSYDVEAAPLNEEVVLVRFLVKEGACRSEGATATEAATYAIDVRGWRILAVQR
>NZ_CP022203.1|WP_095956564.1|39339_39834_-|YkgJ-family-cysteine-cluster-protein
MPLNTLCLRCGMCCDGTLFTHVSLQPEEALALRRRGLAVGSRTDGTPALMQHCSALDGRACTVYTDRPASCRRYHCQLFAALAEKEVSLEEALAVVDEAHARVDAVARTLAPAAEGAPRSVLQRARRANLPEHGGPLSSADLATYERAEAYLDTHFRGRLGRRG
>NZ_CP022203.1|WP_095956565.1|40116_42156_+|PilZ-domain-containing-protein
MQTDTLEGLSGRASMLGYRMGTELTAVASFGNLQAPCRLVQLSLEHLTLNLGTQAAPKPGETASVVLGHGERWATALDAEVMDVRGAPEVSLRFLAPPLDAGRRIVSVLEALRDNGLLLPPETRPVWKERIDHPDRVRRICDALVGRQARGMARAADGRKVPVTAASFDAHEGLLGWRFEGELPAQPFTLEAFGYSSVVHLEVSEAREASGLVVMPLPRELVRYRHRWLRRAAPSRPCTLSFDHPLWPQVHVRRQVVDLSYEGIAFLTEPGEDLLYPGLRQPVLEVVTEGMAPVRLRAEVRNISSTAAGRRCGMSVRPLDASGAQAWRALVESQMHPATQVEGDWNDATWKLFDGSGYFRLPGKAPEDFEDAHPRFDATLARLEGRTRLGYRVVHPEGQSVGATLSVVKPYEGSWMAHQLARQPVKGSRTSAREALRDIYLRGYEPTQVDPEVKWFFAFCEARVRWVRFTKFDFATWYEHTGQTCLVPFQLMEAEVDGAWEIPAGIEVGTPTEAEREAFFDQVARTRPLAYREALDLVPERFDLKRAKERWGEAGLGRERELVVARHEGKPVVLAVLETAQPGLNLFNVLDGVRLVPLVDDATKEAQDAMVALLAHAADWYRARERKVFIHYVEASCVEYVERASLADLGEGKLWVISASLLPEFLEHLFEATTPPAGA
>NZ_CP022203.1|WP_095956566.1|42172_43129_-|NYN-domain-containing-protein
MNGRNAEHRIALFIDFENLVTNTGISSASFDLQPSLDRLLEKGKVVFRRAYCDWSRFAEAKIRLHEFGVELIDVPPSTRAGKNGADMRLVIDALELCYARESIDTFVIGSGDSDFCPLAYKLRENGRTVIGLAVKESTSPLFVKACDEFIYLRPRQSRSDKGDKGRQSVSAEEAGHGKRGGRPGRDEKGRGDKEKAAQGGGKSQSKTEVPDIAREVVQSMLARATGPVNPSLIKEAIVRKEPDFDEREHGFSTFARLLAALEQERLLRRIQQGRQWYVVAADFDMGGGDGKGKKRGPAHAAEEDDELESYPDPDEDEG
>NZ_CP022203.1|WP_157757415.1|43437_43647_+|hypothetical-protein
MLDTKKVVRIICLMLLGTLGGCAPSSAGDAVSTVITDTLVGAPVGVTVRVAAGTATLAAGSWCEAAPGT
>NZ_CP022203.1|WP_095956568.1|43736_44894_+|IS4-family-transposase
MLVRKVAINEEQVRAFLENLFEEDLHAKRVLSLSHATLGVVHAASLSVHAIGQALAWARGGVQKHGIKQVDRLLSNEAVDVWKLAASWVPYVLAERTEAVVALDWTDFEADDHTTLVASLVTSHGRTTPLLWLTLKKSALAGNRAQAEDELLLRLKECVPEGVQVTILADRGFADQRLYALLAQAGFEYVVRFRKDVRVEVEGGHQRPAAEWIPASGHAKKLTEVHVTADRTPVPAVVLVHQKGMKEPWCLATSLGAASARQVVDLYARRFSCEETFRDVKDLRFGMGLSTVRVKSPERRDRLLLVSALAQVLLTLLGAAGESLGMEKGLKANTVKTRTYSLFRQGCMYYQAIPMMKEERLRPLVERFAELLRHHPVFKEALGFI
>NZ_CP022203.1|WP_095956569.1|45240_45831_+|tetratricopeptide-repeat-protein
MTREVLVEKTHATLSDAEKRRISKRIDALFAEAQWGELDQLLSGSLRGTSDDHWLHVRRADAWYAQGKYARAERLFQQVLRAMPRCPLARWGLANTRMARGNAEDARKLFLSLARQKPEVMGTGACGEGVRWARGLVADAHFRLGQLEEQAGATAAARRRYQAYLRILQQPAFSLESRKAANTRLRALGLPKQARR

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Crispr_ID: NZ_CP022203_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_2

1607127-1607219

Orphan

Consensus_repeat	Method
CGCTCCAGCGCGACCGCGCCTGCG	CRISPRCasFinder

1 spacers

WYL

The CRISPR arrays of NZ_CP022203_2

>merge|NZ_CP022203|2|1607127-1607219|CRISPRCasFinder
CGCTCCAGCGCGACCGCGCCTGCGCGGGTCGCCCCGAAGACCACGCCCCCGGCGGACTCCGCGAGGGCTCGCTCCAGGGCGACCGCGCCTGCG

>NZ_CP022203|2|1|1607127-1607219|CRISPRCasFinder
CGCTCCAGCGCGACCGCGCCTGCG	CGGGTCGCCCCGAAGACCACGCCCCCGGCGGACTCCGCGAGGGCT
CGCTCCAGGGCGACCGCGCCTGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095957483.1\|1615293_1616862_+\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|379873
NZ_CP022203.1\|WP_013935517.1\|1596043_1596688_-\|DUF3332-domain-containing-protein	unknown	unknown	gnl\|CDD\|371739
NZ_CP022203.1\|WP_095957477.1\|1599141_1600863_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|283060
NZ_CP022203.1\|WP_013935503.1\|1609168_1609594_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013935499.1\|1613338_1614361_+\|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl\|CDD\|379100
NZ_CP022203.1\|WP_095957481.1\|1604149_1606159_+\|c-type-cytochrome	unknown	unknown	gnl\|CDD\|225926
NZ_CP022203.1\|WP_095957475.1\|1595367_1595943_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013935501.1\|1611415_1612549_+\|glutamate-5-kinase	unknown	unknown	gnl\|CDD\|235460
NZ_CP022203.1\|WP_043709040.1\|1606182_1606782_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095957480.1\|1602420_1603950_-\|two-component-sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|274368
NZ_CP022203.1\|WP_050989106.1\|1609641_1611318_-\|GTPase-HflX	unknown	unknown	gnl\|CDD\|274455
NZ_CP022203.1\|WP_095957479.1\|1601722_1602424_-\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP022203.1\|WP_013935498.1\|1614357_1615287_+\|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl\|CDD\|379100
NZ_CP022203.1\|WP_095957476.1\|1596826_1598191_-\|sigma-54-interacting-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP022203.1\|WP_082207308.1\|1612553_1613024_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961500.1\|1607225_1608140_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|237057
NZ_CP022203.1\|WP_095961499.1\|1598481_1599063_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095957482.1\|1608151_1609159_+\|NAD(P)-dependent-glycerol-3-phosphate-dehydrogenase	unknown	unknown	gnl\|CDD\|234629
NZ_CP022203.1\|WP_043709036.1\|1616901_1618251_+\|cardiolipin-synthase-B	unknown	unknown	gnl\|CDD\|234967
NZ_CP022203.1\|WP_095957478.1\|1601016_1601715_+\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|379312

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095957483.1\|1615293_1616862_+\|FHA-domain-containing-protein	gnl\|CDD\|379873	pfam16697, Yop-YscD_cpl, Inner membrane component of T3SS, cytoplasmic domain. Yop-YscD-cpl is the cytoplasmic domain of Yop proteins like YscD from Proteobacteria. YscD forms part of the inner membrane component of the bacterial type III secretion injectosome apparatus.	1.95571e-20
NZ_CP022203.1\|WP_013935517.1\|1596043_1596688_-\|DUF3332-domain-containing-protein	gnl\|CDD\|371739	pfam11810, DUF3332, Domain of unknown function (DUF3332). This family of proteins are functionally uncharacterized. This family is only found in bacteria.	2.02945e-62
NZ_CP022203.1\|WP_095957477.1\|1599141_1600863_-\|hypothetical-protein	gnl\|CDD\|283060	pfam05297, Herpes_LMP1, Herpesvirus latent membrane protein 1 (LMP1). This family consists of several latent membrane protein 1 or LMP1s mostly from Epstein-Barr virus. LMP1 of EBV is a 62-65 kDa plasma membrane protein possessing six membrane spanning regions, a short cytoplasmic N-terminus and a long cytoplasmic carboxy tail of 200 amino acids. EBV latent membrane protein 1 (LMP1) is essential for EBV-mediated transformation and has been associated with several cases of malignancies. EBV-like viruses in Cynomolgus monkeys (Macaca fascicularis) have been associated with high lymphoma rates in immunosuppressed monkeys.	0.000459239
NZ_CP022203.1\|WP_043709036.1\|1616901_1618251_+\|cardiolipin-synthase-B	gnl\|CDD\|234967	PRK01642, cls, cardiolipin synthetase; Reviewed.	4.35674e-92
NZ_CP022203.1\|WP_013935499.1\|1613338_1614361_+\|WYL-domain-containing-protein	gnl\|CDD\|379100	pfam13280, WYL, WYL domain. WYL is a Sm-like SH3 beta-barrel fold containing domain. It is a member of the WYL-like superfamily, named for three conserved amino acids found in a subset of the superfamily. However, these residues are not strongly conserved throughout the family. Rather, the conservation pattern includes four basic residues and a position often occupied by a cysteine, which are predicted to line a ligand-binding groove typical of the Sm-like SH3 beta-barrels. A WYL domain protein (sll7009) is a negative regulator of the I-D CRISPR-Cas system in Synechocystis sp. It is predicted to be a ligand-sensing domain that could bind negatively charged ligands, such as nucleotides or nucleic acid fragments, to regulate CRISPR-Cas and other defense systems such as the abortive infection AbiG system.	7.63582e-32
NZ_CP022203.1\|WP_095957481.1\|1604149_1606159_+\|c-type-cytochrome	gnl\|CDD\|225926	COG3391, COG3391, Uncharacterized conserved protein [Function unknown].	4.74527e-12
NZ_CP022203.1\|WP_013935498.1\|1614357_1615287_+\|WYL-domain-containing-protein	gnl\|CDD\|379100	pfam13280, WYL, WYL domain. WYL is a Sm-like SH3 beta-barrel fold containing domain. It is a member of the WYL-like superfamily, named for three conserved amino acids found in a subset of the superfamily. However, these residues are not strongly conserved throughout the family. Rather, the conservation pattern includes four basic residues and a position often occupied by a cysteine, which are predicted to line a ligand-binding groove typical of the Sm-like SH3 beta-barrels. A WYL domain protein (sll7009) is a negative regulator of the I-D CRISPR-Cas system in Synechocystis sp. It is predicted to be a ligand-sensing domain that could bind negatively charged ligands, such as nucleotides or nucleic acid fragments, to regulate CRISPR-Cas and other defense systems such as the abortive infection AbiG system.	2.74272e-44
NZ_CP022203.1\|WP_095957480.1\|1602420_1603950_-\|two-component-sensor-histidine-kinase	gnl\|CDD\|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	2.45805e-54
NZ_CP022203.1\|WP_050989106.1\|1609641_1611318_-\|GTPase-HflX	gnl\|CDD\|274455	TIGR03156, GTP_HflX, GTP-binding protein HflX. This protein family is one of a number of homologous small, well-conserved GTP-binding proteins with pleiotropic effects. Bacterial members are designated HflX, following the naming convention in Escherichia coli where HflX is encoded immediately downstream of the RNA chaperone Hfq, and immediately upstream of HflKC, a membrane-associated protease pair with an important housekeeping function. Over large numbers of other bacterial genomes, the pairing with hfq is more significant than with hflK and hlfC. The gene from Homo sapiens in this family has been named PGPL (pseudoautosomal GTP-binding protein-like). [Unknown function, General].	0
NZ_CP022203.1\|WP_013935501.1\|1611415_1612549_+\|glutamate-5-kinase	gnl\|CDD\|235460	PRK05429, PRK05429, gamma-glutamyl kinase; Provisional.	0
NZ_CP022203.1\|WP_095957476.1\|1596826_1598191_-\|sigma-54-interacting-transcriptional-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	2.19103e-115
NZ_CP022203.1\|WP_095957479.1\|1601722_1602424_-\|response-regulator-transcription-factor	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	3.45992e-91
NZ_CP022203.1\|WP_095961500.1\|1607225_1608140_+\|hypothetical-protein	gnl\|CDD\|237057	PRK12323, PRK12323, DNA polymerase III subunit gamma/tau.	8.36024e-09
NZ_CP022203.1\|WP_095957482.1\|1608151_1609159_+\|NAD(P)-dependent-glycerol-3-phosphate-dehydrogenase	gnl\|CDD\|234629	PRK00094, gpsA, NAD(P)H-dependent glycerol-3-phosphate dehydrogenase.	3.83085e-176
NZ_CP022203.1\|WP_095957478.1\|1601016_1601715_+\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	1.21568e-09

>NZ_CP022203.1|WP_043709040.1|1606182_1606782_-|hypothetical-protein
MRVGGRAALFMALALAACRSRPADPPAADAGGAATPIERAAVPDCEVLLSENDRELMLPGFTMKQERACPTCGPLCSFRSDADPDIAVSIAWDCNARHAQADVHALMAPTLQAGGVEVPALGRAAVRRAPAQGMSQVLAWDDDTPCALVITWLGGETERAVEVARAALIATTPAVLDAGTANGQAPDAGDADAGPTGAP
>NZ_CP022203.1|WP_095957481.1|1604149_1606159_+|c-type-cytochrome
MRRTLLATVVVSMLAAPACEDREAQATWTQASGSVALSRDDAFLYVVDSDNGVLAVVDTARREKVGEVKVGLLPERVAVGADDTVYVSNRGSRSVSVIRRGDWSEAARVAVGVEPVGLSVSPTGDTLYVVNSTSRESSRHGSLMAVDTRSLAVRWELPVGDEPRGIALAQGGKRALITRFRQGDLISVDLTDADRPRVAREKTDLYARANTRDGAAASPDGLTPLPPSPDIRFQPRGMSSVAVTPDGERALATVMWAREDPLSPDGTPTPPTGGSLYGGGGPCNTGGVVAPGLVTFDTDTGTPRVDDLDRCRPPPELAPDFPPSTIISPESTHPIQGPVAAVVDPTGLWAFVVNRETDNVAIIPTGRRSGSDLMSGMGSTVRQLVRVGSGPTGIAMTRDGRRAYVYNAFDHTVTTLVSDGAGGTANVRTEGAPLPIAGDVLAPNEVAGRKLFFSALDSRMASTSVGASCASCHPDGREDGHVWGFPDGPRQTPSLAGRGMTKTGPFHWSGEFSTMRDFLDATVRHRMGGTVLDGVMVAQLSDFIDVLPAPDNPHKGEVLTEAQARGEAVFRKAACDACHGGEHFTLNTQADVGTFVTTGPLQDNAAVREVGLNTPSLLGLARTAPYLHDGSAASLKDRLLQGRESNQHGVTAQLTDAEVDDLVEYLLTL
>NZ_CP022203.1|WP_095957480.1|1602420_1603950_-|two-component-sensor-histidine-kinase
MSRTPPRFLNFRRTFALLIVLVVVPSAGLSGFGVVAIINERAAVEKRLEAAWRGTLESLSEELPRILASASLEAVEGRLQFILPDGQSVSEPEGGFELEEGQVRTRDPQLTEALTAVLPEAGGLPTEPTVFSLTTGGRAVLVAAERRGPVVHGVRLSVQALEARLAERVDSRAVSSEPVRFALLPVPRDTSEGGLMGRLVSEVAQARASALGPTGLAERVLPSPLQDFRLVVLPTGEDPVARASTRNRVLYGVLLGLFYLTLTFGVVYTGRALYREAQLSRMKTDFVSLVSHELRTPLTSIRMFIETLALGRLKDPAQMQEVLTLLMRETERLSIFVERVLDWARIEGGRKVYQREMVAVPELVGAAVEAFRTQRMEDGVDLSVDVAEGLPRVDVDRAAVAGALLNLLQNAYKYSGPDNRRITLLARGGGKWVDLSVEDNGVGIAAKERKRVFERFYRVDNLLTRRTEGSGLGLAIARRIIEAHGGRISVQSEPGKGSRFTIQLPAGKA
>NZ_CP022203.1|WP_095957479.1|1601722_1602424_-|response-regulator-transcription-factor
MSSDKTRRILVVEDDLSILTGLSMNLRFEGYEVLQAQDGRTGLARALDESPDLVVLDVMLPELNGFEVLKELRQRGRDTPVVVLSAKGLEPDKILGLNLGADDYVVKPFGLQELLARIKAVLRRRYPSAGAGSPPPVTFGDVSVDMAARTVARAGTPVELTAQEFKLLAHFLAHPGRTFTREELLSGAWGYHYEGSARTVDNFMRQLRLKFEPDPEAPRHFLTVRGLGYRFER
>NZ_CP022203.1|WP_095957478.1|1601016_1601715_+|class-I-SAM-dependent-methyltransferase
MGGHDARGRMPLSLVGQEPDLLFYTRQAAEHGGPVLVLGAANGRVVWALAGHGFDAVGVDPSEVMIRSAEEQRSTEPEDISRRARFQVADLRSLRLPERFPLILAPQHALGLMPGKDDLEALLATVRHHLTPEGTFVYDVLNTPREPVLPRDDEAPSAGLEPRRPLFALHLRERRQPGGPSPIRRLKLRHFTPEELDAALTAAGLVPRERYGRFDGKPFDLEDSRHIGIAGP
>NZ_CP022203.1|WP_095957477.1|1599141_1600863_-|hypothetical-protein
MNTTAHFGPSDFPAGDGDEMKRGWGWAGALFMAGVVGATGCGSGSDSTGAEDLDVPPVQSPQNPEGDAGTPDSGIPGEPDSGAPDDGGTPDDGGTPDDGGTPDDGGTPDDGGTPDDGGTPDGGPVEVPLPTPSAANWEFFGREAGGPRFIHGVTADASGNIWVAGGEEGLFLMKKGERTFRKFTMADGLRPYGYMPDGSVPPGPKYLKVISVAGGWNDTVFVGYEGMPGDGALHCENNWDGNAPDPARYKSGDADRVSLRADGTLDVVHYDISSGPNVVDAELRGREKLCNIWRIAYDANTNSVWFGANHGFARGDADYQGNPTCNGQLLCSGVEEHSHPGINAYIYADPAGDRQRYGEDRSQWSVRDALLTDAYYGLGVRPDGDVWVGGANRTTRYFYGSVGNDFWEGQTRTESAAYAWNRIDIWKDAVGEERYSRPEERTDDLVSGIALMGSSVWVGSFGHGIAELNDSGQVVRTLKNELAAPHVASVAADPANGSIWAGHSWGGGLSRVHGGSVTLYGLSVFGRELSTLRVPDIQVDRSGPRRRILVAFQGATLSDGTVMPGTIGIYSGD
>NZ_CP022203.1|WP_095961499.1|1598481_1599063_+|hypothetical-protein
MPDARPEVKPVLGNRDELIDALRQRLAGSFRWASVSVALGALAVLYGASSFQQALDSGRYRWPFSAQLPVWGSLLIVIGLVAFWLAPRYTRRLVRSVESDVRTELRMTVERKRVPGDDEHFLFVATLYTPDQRHVVLRNVHFHQGDKPLQYPYKKGVTQIPVQVYGRPGEGPIVIDAGWGFLLPANLTYPWYK
>NZ_CP022203.1|WP_095957476.1|1596826_1598191_-|sigma-54-interacting-transcriptional-regulator
MPVLPPAPIPSHTVIGARTQGERLSAQLFHLVLLDTERAGTVFPLANDALRVGKAADNDVVIDHPTVSRNHLVVRRQGDRFLVQDLGSTNGTFLDGAQVREAFLRPGALLEVGDVRLRFSPQVSPVQVEPILEDRLGDLVGRSLPMRQIFALLQRIAPTDSTVLLVGETGSGKGAAAKATHKLSPRATGPLVVFDCASVSDSLIESELFGHEKGAFTGAVSQRIGCLERANGGTLFLDEIDDLALDLQPKLLRAIEDREFRRLGASTPISFDARIIVASKKDLWAETQAGRFREDLYFRLSVFTVSLPSLRDRKEDIPLLVDAFAGEGLWPRLPEKIREQFTGHTWPGNVRELRNALERARHMVDIPELAGDSLLREFTREAPAAAGDSLPVEFTGPFKVCKDELIRAFEREYLTRLLGRAKGNIARAAREAELDRKHLYSLLHKYGLVQSETD
>NZ_CP022203.1|WP_013935517.1|1596043_1596688_-|DUF3332-domain-containing-protein
MKRPSPWLAMLFAGFMSMHATGCFGQFQLTQKIWNFNKNISGNKFVQWLMFLVLTIIPVYGLGAFIDAIVINSIEFWTGSNPVASVDGAPETTRIVKLSPTDTLRLSRDVETGVMRMELEREGQETMVRYFEPLEDGMVVRDDAGAMLIQAQEATDGAVAVTDAAGTTLTVHARDALAVARRVYEEGGAQALAQHTVAQASMSQGLAANTCVAR
>NZ_CP022203.1|WP_095957475.1|1595367_1595943_+|hypothetical-protein
MTRAVRALAAVGLSALMAGAGLAACGLADNSLGGSVSELFPLEVSRVEVRRNAEAFQVSYYRNNDLDVDLVVRLTVSTEGLDLRPGSKVDLAGTTPSGQARATVVHLNAGEPARVFGPVNKGDLQLESGGNPGESTRGNFSMSFIRGDGYGAGRNLEGTFAVVAQDATFGPEPGQLLDGGVPPPDAGTPPE
>NZ_CP022203.1|WP_095961500.1|1607225_1608140_+|hypothetical-protein
MPAPAPSEATAPAPSGPAGPPPRNPAPDTSWAQPAEVSAPARNEAPDDAAWESFPGATAVPRAEEAATLPRLPEVPPLVPVDDAAIPTPQPAAPVVTRPPPVPNRVSLLGARTVGEGGLAAGLSLGFPTVSARVAVGVLRRLDVLAGVDSAYGLMNELRLGARWMVFDGGPRWSLGVAVEGSHAFFLRPASVEDRGARYLSGRRNWNVQPGIVGNFQLRGARAPRLFLDVRYLLTLDTEPIQGVPLGGLPPDVELSSAFPIRVGAEVPVSEKTSYAVTLGGDIRTRPDEADFMPVISFGVVTGF
>NZ_CP022203.1|WP_095957482.1|1608151_1609159_+|NAD(P)-dependent-glycerol-3-phosphate-dehydrogenase
MRGSVIGSGSFGTALANVLAVNCEEVRLWGREASVVEAINAQHENPTYLKGIPISERVRATTNLEEALAGSELVVLATPSHATREVVARAQAYLPRHVPIVTVSKGIENETLLTMTELLEDCLPEEFHPYLAVLSGPSFAKELARRMPTVVTIASHWDKVALRCQKALQTETFRSYTSTDVVGVQYGGALKNVIAIAAGMADGLGMGHNARAAIITRGLAEITRLAVRKGANPLTLSGLSGMGDLVLTCTGELSRNRHVGMELGKGRKLPDILADMKEVAEGVKTARSARDLELKTGVELPICHQVYLIAHEGKSARSAVVDLMTRQPKSELAGV
>NZ_CP022203.1|WP_013935503.1|1609168_1609594_-|hypothetical-protein
MSIPTLTPLLLAQADYAKPVSSLSPKYIELLEQNSHIIYPIVAILTLVIIAAGVLQAWRTQDLDGLQKNEFKRAIVNELRRNISGMPGDLLAKSVGLDRLKTNRLLEQMQQEGLVVSHTNSQRLTVWRVRGATPDAAPRRY
>NZ_CP022203.1|WP_050989106.1|1609641_1611318_-|GTPase-HflX
MPPPGEHGLKEIYGNTLGLKSSEQHRLRNTFRRRVPPHEIVSPELARHLTELSRETNRQVGVLVNRKGEIEHVIVGNAHKLELPDIGRARAGQVRLRGLRLVHTHLKSEPLTKDDLTDLALLRLDCVAAIGVEHDGLPGVLHYAYLVPENGSGEFWNVESLPSVHVAQPDLMDTLGALEEEFNRKAASRKVGGREKAILVAVCLDGNRALAESSLAELKELARTAGVEVIDSVLQVKREADPRYLIGRGKLEELNLRSMQSMVDLLIFDKDLTPSQGRHIGEATSLKVLDRSQLILDIFAQRAQSAEGKLQVELAQLKYRLPRLVQSDDSLSRLMGGIGGRGPGETKLEIDRRRVRERITHLEKRIDAIGRERSVRRAQRNRRELPVISIVGYTNAGKSTLLNAITNAEVLAENKLFATLDPTSRRLRFPQEREVIITDTVGFIRDLPKDLVAAFRATLEELYDASLLLHVVDAADPARDEQVEAVENILDSLDLMEKPRLMVWNKADLLPQDEVEALLRTRGGVAISAATREGLATLLAKADTTLFAEGATEAIGAV
>NZ_CP022203.1|WP_013935501.1|1611415_1612549_+|glutamate-5-kinase
MSWISTGRTALRAARRVVVKIGTNALTNATGRFNRHHFDALGQDLLWAAQGRELVVVSSGAIALGVERLGLPSRPRDIPGKQACAAVGQSRLMQAYEEAFAARGKAVAQVLLTHEDVQERRRYLNVKHTLERLLTAGVVPVINENDTVSVDELKFGDNDTLAGLVAGVVEADALVLLSDVEGLYTGDPRRDADAELLATVLQVTPEVLALATGTTSGVGTGGMSTKVRAAARASESGIHCVITSGAVPGRLRAVLEGEDVGTLFEPTGSRRSARAAWIAHALRARGTLTVDAGAREAIVTGKRSLLPSGVRGVEGDFGRGDPVDLVGVDGAVFARGLAAYDANELRRIAGRHTADIEAVLGYRYLDEAVHRDDLAVL
>NZ_CP022203.1|WP_082207308.1|1612553_1613024_-|hypothetical-protein
MSRITLVRNVVAGLAMFVGVTSTAAPAPVRAEPLYFAVEVRRDGRLVAQPKLLGETGRTLRAERRRPGAPLPDYRLVLTPRAEGKSFLLQLDLQLPEAKGHSELALLHGQERKLQLGSVPGELEVSLLLMKVDSPEFRALMQLGESSGASSSTSSI
>NZ_CP022203.1|WP_013935499.1|1613338_1614361_+|WYL-domain-containing-protein
MDRTERILDLVALLLDAREPISWAELREHFPADYGGSDDAAERKFERDKAELVELGFPLTYVQGDDERRDGYIVDRDAYYLPEADLSKEELAVLYAAGSAALASGAFPGRDDLAHALRKIGFFAGQSLPTPRVRMELGSVHEGQEKEVSARLEQLWDACAARKWVDVTYASPKQAGTTQRRVDPYGLALRRGAWTLVGYCHLRASLRSFHVHRIRELKVNTARPRTPDFQVPADFSLDSHVAYFPWQHRFHEQVEVVLHLSGTLASRAASLLPGAALEPAEAGAVRARLPVTFVDGLLRFCLALGPDCRVEGPERAQARLREMASRIVASHEDSQDKVSA
>NZ_CP022203.1|WP_013935498.1|1614357_1615287_+|WYL-domain-containing-protein
MSNVHERLRRLLFLVPYVSKHPGVTVDALARALNVSREDLLEELDLLTCVGRPPFNPDDYIDIYVDNDRVYVDLDQRLFAPPRLTPGEAAALAASAELLRPATGDALQSALQKLERVLPPATRERYREMYRKIDASTEAPQALGPLTRAIIERLEVTFGYASPGRSPEPRTVRPYELLSHRGQWYLQGYCHTRQDARLFRLDRMEDITVTDVPFQPPADARADVPNPARGLTDASVRVRFSPVAAPYVKERFGRDARPLADGGVEVLVAGDSERWLTQWVLSFGGEAQVMEPASARAAVARAARASVGL
>NZ_CP022203.1|WP_095957483.1|1615293_1616862_+|FHA-domain-containing-protein
MPFQLTISEGREAGKEFVFDQDSVLIGRSTDCDVALFDPGVSRRHCRIFLDGDAYSVEDQGSANGSLVNGSPVKTQVLEDGDKLTLGPVTFIFAMLTDEPATGEEELPAGAQEGDGSTRIVSLDSLKRQRNKGVALAPEGADQDELDEIREGATRNNLQALRPVSQGQSGSRPAAIERSAPAAAPARRPASAPPPARARPAPSAGGGGLSAAERARIRRESPGIVSSAKLFWADASQGVRTGIIGGGVALVLGLFGVLYWLVLSGEDGQPVGEEPAWLSGQPIRDGFGLGPGATWERADMKVFEWEYTAATRAVVILHYQAQGISKDEVVVSVNGVDVGKVPPDTLASQDRSIELMIPAQHLKKGEPNRIIFDNVKNPPGEDPWVIWNIWVERALLPDLLPEELVREATEYHKRGLKHFQTPDIGARNRYEAWKSFRVSWLMLEAHPEPKPDLYYDAQERMKAAQQELDRTCSKLLLEVEGYYNQGNYKSASATLDHVKEYFPEYDQPCATRAEAKRAEYGL
>NZ_CP022203.1|WP_043709036.1|1616901_1618251_+|cardiolipin-synthase-B
MSRRFPDTGWHRQTGCEAARVAGSRGRPHRWEAMGEPEALTEQSGEADTGAPTPPGPVPEHGPVWSPNVSGLLLSRYYLPRRHPVMQGNACQLLRDGVEAYPAMLEAIRGARRYVRLETYMFVSDAVGELFGEALAQAAERGVHVKVLYDAVGSWTSRRSFFAGLRARGVDIRAFKPFSLSRGLRHLLRRDHRKILVVDGEVAFTGGVNISAHWAPAGVGAAWRDDVLRIEGPAVHELERCFSATWRMMFQGRFHRLTRRLERLRRQPSRQGGVGLAVLSSRRSIHRAYLHAIRRARRSVLVAAAYFIPDRRMVMALREAARRGVEVHLLLNARSDHPLLEFMARGFYERLLGAGVRIFEWQRGVLHAKTAVVDGVWGTIGSFNLERLSLAFNHEVNAVFADPRLGQQLEDSFRGDCGDCREVTLAEFRRRPLWQKLLERALLLLRKII

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Crispr_ID: NZ_CP022203_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_3

2359053-2359156

Orphan

Consensus_repeat	Method
CTCGGCCGGCCCCGAGACGGCGGGCGGTTTCTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022203_3

>merge|NZ_CP022203|3|2359053-2359156|CRISPRCasFinder
CTCGGCCGGCCCCGAGACGGCGGGCGGTTTCTTGTAGGGCGCTCCATGGGGGAGCTCCCGACGCCCACCGCCTCGGCCGGCCCCGAGACGGTGGGCGGTTTCTT

>NZ_CP022203|3|2|2359053-2359156|CRISPRCasFinder
CTCGGCCGGCCCCGAGACGGCGGGCGGTTTCTT	GTAGGGCGCTCCATGGGGGAGCTCCCGACGCCCACCGC
CTCGGCCGGCCCCGAGACGGTGGGCGGTTTCTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095957937.1\|2347098_2348379_-\|serine--tRNA-ligase	unknown	unknown	gnl\|CDD\|235461
NZ_CP022203.1\|WP_095957943.1\|2359711_2363533_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP022203.1\|WP_095957940.1\|2355874_2356813_+\|polysaccharide-deacetylase-family-protein	unknown	unknown	gnl\|CDD\|200565
NZ_CP022203.1\|WP_013938559.1\|2366029_2366281_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|378598
NZ_CP022203.1\|WP_095957944.1\|2363902_2365984_-\|ATP-dependent-DNA-helicase-RecQ	unknown	unknown	gnl\|CDD\|223588
NZ_CP022203.1\|WP_095957939.1\|2355146_2355857_+\|glycosyltransferase-family-2-protein	unknown	unknown	gnl\|CDD\|133022
NZ_CP022203.1\|WP_095957946.1\|2368798_2369983_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|99738
NZ_CP022203.1\|WP_013938554.1\|2357833_2358757_+\|SDR-family-oxidoreductase	unknown	unknown	gnl\|CDD\|187551
NZ_CP022203.1\|WP_095957947.1\|2369979_2370474_+\|cyclic-pyranopterin-monophosphate-synthase-MoaC	unknown	unknown	gnl\|CDD\|236483
NZ_CP022203.1\|WP_095957945.1\|2366280_2367051_-\|DNA-repair-protein-RadC	unknown	unknown	gnl\|CDD\|178801
NZ_CP022203.1\|WP_095957941.1\|2356943_2357798_+\|acyltransferase-family-protein	unknown	unknown	gnl\|CDD\|153249
NZ_CP022203.1\|WP_013938550.1\|2353759_2355073_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235967
NZ_CP022203.1\|WP_095957938.1\|2348526_2353530_-\|zinc-ribbon-domain-containing-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP022203.1\|WP_013938557.1\|2363534_2363906_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_170114724.1\|2359157_2359622_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013938547.1\|2346193_2346658_-\|nucleoside-deaminase	unknown	unknown	gnl\|CDD\|223663
NZ_CP022203.1\|WP_013938562.1\|2367739_2368702_+\|thioredoxin-disulfide-reductase	unknown	unknown	gnl\|CDD\|273540
NZ_CP022203.1\|WP_170114809.1\|2344483_2345815_+\|mannosyltransferase	unknown	unknown	gnl\|CDD\|281842
NZ_CP022203.1\|WP_043710497.1\|2342992_2344201_-\|DNA-polymerase-III-subunit-gamma/tau	unknown	unknown	gnl\|CDD\|237871
NZ_CP022203.1\|WP_013938561.1\|2367208_2367667_-\|cyclic-nucleotide-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|237999

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095957937.1\|2347098_2348379_-\|serine--tRNA-ligase	gnl\|CDD\|235461	PRK05431, PRK05431, seryl-tRNA synthetase; Provisional.	0
NZ_CP022203.1\|WP_095957940.1\|2355874_2356813_+\|polysaccharide-deacetylase-family-protein	gnl\|CDD\|200565	cd10940, CE4_PuuE_HpPgdA_like_1, Putative catalytic domain of uncharacterized bacterial polysaccharide deacetylases similar to bacterial PuuE allantoinases and Helicobacter pylori peptidoglycan deacetylase (HpPgdA). This family contains many uncharacterized bacterial polysaccharide deacetylases (DCAs) that show high sequence similarity to the catalytic domain of bacterial PuuE allantoinases and Helicobacter pylori peptidoglycan deacetylase (HpPgdA). PuuE allantoinase appears to be metal-independent and specifically catalyzes the hydrolysis of (S)-allantoin into allantoic acid. Different from PuuE allantoinase, HpPgdA has the ability to bind a metal ion at the active site and is responsible for a peptidoglycan modification that counteracts the host immune response. Both PuuE allantoinase and HpPgdA function as homotetramers. The monomer is composed of a 7-stranded barrel with detectable sequence similarity to the 6-stranded barrel NodB homology domain of DCA-like proteins in the CE4 superfamily, which removes N-linked or O-linked acetyl groups from cell wall polysaccharides. In contrast to typical NodB-like DCAs, PuuE allantoinase and HpPgdA do not exhibit a solvent-accessible polysaccharide binding groove and might only bind a small molecule at the active site.	4.54093e-113
NZ_CP022203.1\|WP_013938559.1\|2366029_2366281_-\|hypothetical-protein	gnl\|CDD\|378598	pfam11213, DUF3006, Protein of unknown function (DUF3006). This family of proteins has no known function.	0.001324
NZ_CP022203.1\|WP_095957944.1\|2363902_2365984_-\|ATP-dependent-DNA-helicase-RecQ	gnl\|CDD\|223588	COG0514, RecQ, Superfamily II DNA helicase [DNA replication, recombination, and repair].	2.21739e-156
NZ_CP022203.1\|WP_095957939.1\|2355146_2355857_+\|glycosyltransferase-family-2-protein	gnl\|CDD\|133022	cd04179, DPM_DPG-synthase_like, DPM_DPG-synthase_like is a member of the Glycosyltransferase 2 superfamily. 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. In higher eukaryotes,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. In lower eukaryotes, such as Saccharomyces cerevisiae and Trypanosoma brucei, DPM synthase consists of a single component (Dpm1p and TbDpm1, respectively) that possesses one predicted transmembrane region near the C terminus for anchoring to the ER membrane. In contrast, the Dpm1 homologues of higher eukaryotes, namely fission yeast, fungi, and animals, have no transmembrane region, suggesting the existence of adapter molecules for membrane anchoring. This family also includes bacteria and archaea DPM1_like enzymes. However, the enzyme structure and mechanism of function are not well understood. The UDP-glucose:dolichyl-phosphate glucosyltransferase (DPG_synthase) is a transmembrane-bound enzyme of the endoplasmic reticulum involved in protein N-linked glycosylation. This enzyme catalyzes the transfer of glucose from UDP-glucose to dolichyl phosphate. This protein family belongs to Glycosyltransferase 2 superfamily.	7.51832e-39
NZ_CP022203.1\|WP_095957946.1\|2368798_2369983_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|99738	cd00614, CGS_like, CGS_like: Cystathionine gamma-synthase is a PLP dependent enzyme and catalyzes the committed step of methionine biosynthesis. This pathway is unique to microorganisms and plants, rendering the enzyme an attractive target for the development of antimicrobials and herbicides. This subgroup also includes cystathionine gamma-lyases (CGL), O-acetylhomoserine sulfhydrylases and O-acetylhomoserine thiol lyases. CGL's are very similar to CGS's. Members of this group are widely distributed among all three forms of life.	2.73263e-133
NZ_CP022203.1\|WP_013938554.1\|2357833_2358757_+\|SDR-family-oxidoreductase	gnl\|CDD\|187551	cd05240, UDP_G4E_3_SDR_e, UDP-glucose 4 epimerase (G4E), subgroup 3, extended (e) SDRs. Members of this bacterial subgroup are identified as possible sugar epimerases, such as UDP-glucose 4 epimerase. However, while the NAD(P)-binding motif is fairly well conserved, not all members retain the canonical active site tetrad of the extended 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. Extended SDRs are distinct from classical SDRs. In addition to the Rossmann fold (alpha/beta folding pattern with a central beta-sheet) core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids. Extended SDRs are a diverse collection of proteins, and include isomerases, epimerases, oxidoreductases, and lyases; they typically have a TGXXGXXG cofactor binding motif. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	2.76828e-115
NZ_CP022203.1\|WP_095957947.1\|2369979_2370474_+\|cyclic-pyranopterin-monophosphate-synthase-MoaC	gnl\|CDD\|236483	PRK09364, moaC, cyclic pyranopterin monophosphate synthase MoaC.	4.29362e-75
NZ_CP022203.1\|WP_095957945.1\|2366280_2367051_-\|DNA-repair-protein-RadC	gnl\|CDD\|178801	PRK00024, PRK00024, DNA repair protein RadC.	2.52974e-77
NZ_CP022203.1\|WP_095957941.1\|2356943_2357798_+\|acyltransferase-family-protein	gnl\|CDD\|153249	cd07987, LPLAT_MGAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: MGAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this suubgroup are such LPLATs as 2-acylglycerol O-acyltransferase (MGAT), and similar proteins.	1.47178e-43
NZ_CP022203.1\|WP_013938550.1\|2353759_2355073_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|235967	PRK07208, PRK07208, hypothetical protein; Provisional.	1.72977e-44
NZ_CP022203.1\|WP_095957943.1\|2359711_2363533_+\|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.	1.50853e-23
NZ_CP022203.1\|WP_095957938.1\|2348526_2353530_-\|zinc-ribbon-domain-containing-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.	2.42955e-38
NZ_CP022203.1\|WP_013938547.1\|2346193_2346658_-\|nucleoside-deaminase	gnl\|CDD\|223663	COG0590, CumB, Cytosine/adenosine deaminases [Nucleotide transport and metabolism / Translation, ribosomal structure and biogenesis].	1.94346e-67
NZ_CP022203.1\|WP_013938562.1\|2367739_2368702_+\|thioredoxin-disulfide-reductase	gnl\|CDD\|273540	TIGR01292, Thioredoxin_reductase, thioredoxin-disulfide reductase. This model describes thioredoxin-disulfide reductase, a member of the pyridine nucleotide-disulphide oxidoreductases (pfam00070). [Energy metabolism, Electron transport].	3.13639e-153
NZ_CP022203.1\|WP_170114809.1\|2344483_2345815_+\|mannosyltransferase	gnl\|CDD\|281842	pfam03901, Glyco_transf_22, Alg9-like mannosyltransferase family. Members of this family are mannosyltransferase enzymes. At least some members are localized in endoplasmic reticulum and involved in GPI anchor biosynthesis.	1.58097e-23
NZ_CP022203.1\|WP_043710497.1\|2342992_2344201_-\|DNA-polymerase-III-subunit-gamma/tau	gnl\|CDD\|237871	PRK14965, PRK14965, DNA polymerase III subunits gamma and tau; Provisional.	0
NZ_CP022203.1\|WP_013938561.1\|2367208_2367667_-\|cyclic-nucleotide-binding-domain-containing-protein	gnl\|CDD\|237999	cd00038, CAP_ED, effector domain of the CAP family of transcription factors; members include CAP (or cAMP receptor protein (CRP)), which binds cAMP, FNR (fumarate and nitrate reduction), which uses an iron-sulfur cluster to sense oxygen) and CooA, a heme containing CO sensor. In all cases binding of the effector leads to conformational changes and the ability to activate transcription. Cyclic nucleotide-binding domain similar to CAP are also present in cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) and vertebrate cyclic nucleotide-gated ion-channels. Cyclic nucleotide-monophosphate binding domain; proteins that bind cyclic nucleotides (cAMP or cGMP) share a structural domain of about 120 residues; the best studied is the prokaryotic catabolite gene activator, CAP, where such a domain is known to be composed of three alpha-helices and a distinctive eight-stranded, antiparallel beta-barrel structure; three conserved glycine residues are thought to be essential for maintenance of the structural integrity of the beta-barrel; CooA is a homodimeric transcription factor that belongs to CAP family; cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) contain two tandem copies of the cyclic nucleotide-binding domain; cAPK's are composed of two different subunits, a catalytic chain and a regulatory chain, which contains both copies of the domain; cGPK's are single chain enzymes that include the two copies of the domain in their N-terminal section; also found in vertebrate cyclic nucleotide-gated ion-channels.	7.76046e-30

>NZ_CP022203.1|WP_013938554.1|2357833_2358757_+|SDR-family-oxidoreductase
MKPAVVVTGISGNLGRTLAKLLHKHERIIGIDRRPFMGRPKDVEMYELDLRKKKAEDVFRKNEIRAVIHMGIMHDPRMSEEEHHSFNVVGTTRLLEYCAKYGVKKVVVLSSANVYGPSPDNSNFLTEDAPLMAASRFSGVRDLIEVDMLAHSFFWKHPHIETVILRPVHIVGPTIKNAPSNYLRMRRPWMMAGFDPMVQLIHVEDVARAMVEALRPEPKGVYNVVGPGEVPLSAVMRELGNTPIPVPHPVARPLLGMLFKYRLANFPPPELDHIQFLCAVDGSRWVKDVAWKPRHSMRDTIRSVQGD
>NZ_CP022203.1|WP_095957941.1|2356943_2357798_+|acyltransferase-family-protein
MLENVTDRLKKGLREWTDRLANDEQKQRLQALARPGNEYGVDPFGFDLDYSLSAVAPLLWLYRNYFRVETYGIEHVPAGRVLLVSNHSGQLPMDGAMIGVAMMLEASPPRPIRSMVEKWVSSLPYVSTFMARVGQIVGTPENCRRLLESEEAILVFPEGTRGINKLWPQRYQLQEFGLGFMRLALETNTPIVPVAVIGAEEQAPALMDLKPVAKLLGFPSFPITPTGLPIPLPTKYRIYFGEPLHFSGRPDDEDSELDKKVRTVKASIQSMLHQGLKERQGVFW
>NZ_CP022203.1|WP_095957940.1|2355874_2356813_+|polysaccharide-deacetylase-family-protein
MRLASISVDLDSLPHYCRIHGLPEAMLDDRARSLVHAVAVPRFRELLDGLGVPGTFFVIGEDLETDPAAAVGMRASHEAGIEVASHSHAHDYALTRRGPAAIQEDLARADAAIHQATGVRPVGFRAPGYTLNADLYAATAALGYRYGSSAFPAAPYYAAKAAVMGGLAMLGRPSRSVLDTPRVLLAPRVPYRPDPAQPYRRGTGSVLELPMTVTPALRFPLIGTFATTLPRASLHALWRTCRRDRFFNFELHGVDVLDASDGIPPELVRQQRDLRVSATQKMARLREVFGWLKAEREVLTLRDVAGRLASTV
>NZ_CP022203.1|WP_095957939.1|2355146_2355857_+|glycosyltransferase-family-2-protein
MAPHLTVVIPVYNEESIIASAAEELRQGLEARGLDYEIIFAENGSRDATPAILEELCAKNPRLRWFHSETPNYGVALKAGILKARGTYVICDEIDLCDLTFYDAALPRLERGEADMVVGSKAAKGASDQRPLIRRAATRVHNKLLKVALGFQGTDTHGLKAFRREALLPVIQKCVVDMDVFASEFVIRAWREGLRVVEIPIQLQEKRQPSIHLFKRVPNVLKNVGKLFYVIRVRGT
>NZ_CP022203.1|WP_013938550.1|2353759_2355073_+|FAD-dependent-oxidoreductase
MEPIVILGAGLAGLSTAHFLTKPWRLIEKSDRVGGLIKTEVIQGCYFDPTGHWLHLRDPEIQALVNTLWLPEQMVRIQRKAGIFTRGVFTRFPYQVNTHGLPPEVVAENLTGYVEAIYGEKGRELREREPRNFEEFILRYMGEGFAKNFMVPYNQKLWTVHPREMSAAWVGRFVPRPNLKEVVDGALGAGSDAVGYNASFLYPREGGIESLARAMLSHLKGGQLSTHTEPTAIDWKARKVTLSDGTVQPYAGLVSSISLPGLVKLLAKGEAGVPDAVQDAARKLRATTVTYVAVGAKGANRQPWHWIYLPEPEFHTYRIGSPSAVYAPLAPPDTSTFYVEYSHHGELSPAAAEQYAVEDLVRSQMIHAADDVLFAQAREIPHAYVLYDEAYGPAKSEILRFLEHAGVQIAGRYGQWEYSSMEDAILAGRACARTLNG
>NZ_CP022203.1|WP_095957938.1|2348526_2353530_-|zinc-ribbon-domain-containing-protein
MKVSCPSCQTNYNIDDKRIPPGGAKLKCARCQTTFPIKLEAVSAPPAPAPAEPAVPLPGAPAPAPRSAAVPLPGAAPDASAAPAAAAVPLPGAAPAHPATAAVPLPGAPASAGAIPLPGAAPAPAAVPLPGAVPPPGAAAPAASAIPLPGAAPAASAAIPLPGAAPAASAIPLPGAAPAHLAASAAIPLPGAPASAGAIPLPGAPAAGAIPLPGAAPAHPAASAAIPLPGAPVSSSAIPPPAAPDASGAIPLPGGAPEADPFAFDMSEAPQAASIPLPGGAPEADPFAFDMSEAPQAASIPLPGSAPEEDAFAFDMGAPAEAAVPPPGAAPEEDAFAFDMSSPAEAAAAMPPSDGLDAFGDDPGEPARDTREVTRVVSIPLPSDAYREPPAPAASGYGVNEPAGTARDFDFDTVEAPAEDATQGYGVNEPAGTARDFDFASDDALPVPVEAPPAEDAFAFDIESPGAAAQPPQDDPFALPPPPAHAQPAAPQDDPFALPPPQDDPFALPPAPDAYAMPAAPAAEPYAMPPPAAGAPSFDFAELPVPANADPFALPPPGAADFSDLPAPAAPQALEFADLPAPAAPAPDLSFDFNEPPAPGADPFAADFGSAPAPAPAADPFAADFGSAPAPAPAADPFAADFGSAPAPAPAADPFAIDFAEPPAPAPAVAVNPALDFGDVDFGSPPPAASPSIPDSLEFDPTARPDDDLEADLSDPLPPPPNAGPADGLEMLSFIDDAAGKDGGAQAGAKVRRFHVRRRSGKVFGPFDEGVIVKMLEDGQLLGNEDVSQDSETWSAIGTVPTFAAAIQRLMEGPAKLVTPAAAPAAAVVDAPRVDGVDPQANMKRLEQLYEGRMAAVSVVDRSGNTEKWKKRIPLMIAAGVAVVVAGIGAGTEFGTRYGAFGRKALFPPRVADGSPQAKQVQEAKQALLTDTFDSYKQAREITAKVLQQKEYPEVRSLWCQSVHYLQRRYAAGNPNEMSRCRQDMAEIGFLGEKDVDFIKASAALALTSRQADSVIPALSDAHSREDTQADAELAFLLAEAYAQKRDEKRALDTLKKVLAKNPKSAKAHHAMGNLHQSADRADEAAAAYAAALEADPKHVASAVELAAVELLVRKDVEKGAEAVERALAPDVQSALGPAELARARGLKGVAMFQRHQPKEAEAELKAALEMDEKSAFLRGQLARVLRAQRNFDGALPIYKALSVEEPNNLEFADGHITALVMTGKMQDALEAVTKANGVFPNEARIAYLFGRIEDALDKLSDAEGHYKRAIAADENLVEARLYLGRFYLAQRRNAEARAQLEEAVKKAPEHAGVRAGLGELALAENNALLAQQEFERSVKLDPILADAHLGLSRVALLTDDLETAKTEANRALELDPHLLKDGRLQRGLVLWRLGQLEEAVAELEKAKTEDPRSTTIPITLGAVLLERGDLPGAESNLGLALSNEPSNHEALYYLALVKAKRLEFTQALDNMRKAVERAPNRPDYHYAYGVILRDAKNLPDAMDSWRKTVELDASHADAHEALGHAQLESSQFDEAIASFEASLKADPRRTRVMGSIGDAYFAAARWNDAIKRYQSALKADPKLTYVYYKVARAFTEQAQHAKAIDWYRKATNADSENPMAYYYLGFAYKERNKKREAVQAFKDYLSRKPDATDKQDIEDEIYDLQN
>NZ_CP022203.1|WP_095957937.1|2347098_2348379_-|serine--tRNA-ligase
MLDLRNVAQNFDAVVARLKTRGGNLDLGPFQRLFAERRELYVSVESLAARRNAANEEMKRKAKEDPKALDALRGDLRAVSQEIKEKEGRLKDVEEELNRILLLIPNVPHESVPEGGGAEDNVQVAIWGQKPDLLFAPKQHFELGEKLGMLDFERAAKVSGSRFTFYKGALARLERALVTFMIDVHTSKGYTELLPPYLVLRETMMGTGQLPKFEDDVFKTVGEPERFLIPTAEVPVTNYHADEILEGESLPIRYCAFSPSFRAEAGAAGRDTRGLVRQHQFHKVELVKFAQQDKSLDELEAMTDDACDILRRLGLHHRVMLLCTGDMGFSARKTYDIEVWLPGQNAYREISSCSDCGDFQARRAKIRYRAQKGDKPQLAHTLNGSGLAVGRTAIAILENYQREDGSVAIPEALVPYMGGLKELKPI
>NZ_CP022203.1|WP_013938547.1|2346193_2346658_-|nucleoside-deaminase
MSDEAFMQQALSLAREAAELGEVPVGAVAVLDGEVVGTGFNRREVDRNPLAHAEMLAMDAAARKLGAWRLSGVTLYVTLEPCAMCAGGLVQSRVTRLVFGAFDPKAGAVGSLYNLVEEPRHNHRLQVTSGILADESRLLLKTFFGRLRAKKRDN
>NZ_CP022203.1|WP_170114809.1|2344483_2345815_+|mannosyltransferase
MALLPGLIAVVQLGRIHPDEVYQSLEPAWWRVHGYGVLAWEWREGLRNWAVPGVLAGFLKLADLLGITHPRAYRVVVALPQVALHAWSLWAAHRFAQRRAGDTGGLLATLLVGLYGPVLVFAGRTMAESISASLLIVAMEALDRRERLARAGLVGGVALGLAVVARYPSAIFVLAALVWLAAARRWRLLVFTCVGGLAVAVALGALDWATWGKPFHSFFAYVRFNVFSGKAAARFGADPPSFYVKPLLSAVPLWAWAAVPLGAAALRQRRFPSLPLWCAAVYTGVLLATAHKEERFLYPGLVLAMLAAAPPVAALLARRAQPTGRWGLAGLALAATLASAAYFPSGDLRADQFRAIVAATRGNARGLLIVNEGLWGSGGFFYLGKRIPWLTCDWPHDAAFQRALRDKTFNRAVTFEDRALTELQAGGFQVVRKVGRETILSRE
>NZ_CP022203.1|WP_043710497.1|2342992_2344201_-|DNA-polymerase-III-subunit-gamma/tau
MSYLVLARKWRPQKFDDMTGQEHVVRTVANAIKMDRVAHAYLFCGPRGVGKTTAARLLAKALNCEKGPTAQPCGECRACVEIAAGTSVDVAEIDGASNNGVENVREIRENAKYLPQRDRHKIYIIDEVHMLSGAAFNALLKTLEEPPGHVKFIFATTEAHKLPDTILSRCQRHNFRRIPAARMLQRLQEICKAEGAGISDRSLSLVVRQSEGGMRDALSLLDQVLASCGANPSDEEVAEALGAIDRTMVQDFADALVHKDAKRVLERVEEVFNRGLDLKRLAEELAFQLRHLFVTKTLGKAPDELAESEQKALVALAQDAEAAQITRLFDVVHGCIWDVSRAAQPRLALEMALLKAIQLSPGGSIPELLARVDKLAAGLGDGSAKSNAGAPGGRSSPANFRA
>NZ_CP022203.1|WP_170114724.1|2359157_2359622_-|hypothetical-protein
MNRLPALLLALVLGACATVSKKSNLETLKPTVERFHQAIRWKDFQSASRIIVPERRKDFQKARIELNDDKDLSITDYEVVDVKVSADGNQATIQSRIQWMRLPSASERTALVTSEFVFRDGAWQLESQEDGPFEGELPSPSPNPSSSPEETPIP
>NZ_CP022203.1|WP_095957943.1|2359711_2363533_+|tetratricopeptide-repeat-protein
MAKSMVERYEQLLRQDPTSSVFVELAKALLEKGDTARAIEVCGQGISHHPTSIVGRVLWGKALIQQGRPAEAMEQFDQAISIEKDNPYAYNLIGEVLLQRGLYRSALPILRKAVALQPNDGRVKSWLDQAQQALAGGPAPVFADLMGLEKPAADEDTPAEPPKDEDPAPGPTVAPMAAARLRAAALGDAAKLKPASAGAAAAGDSADAGPGTAGVADAGTGADAGTGADGGEASAADPSVARGGEASAADPSVARGGEASAVDPSVARGGAATRPEGSGDEAGASLGLLNRRVPVSSVLGAELPSLDLGLGDDEDAPQRGEDEAPGQALSSEAAAGGPAEDSALPDSTQDSGAGQDAPTQQVALPEGAEAAAASAPEADEDGRQAGAAPAEDGPLAASAPVEDTASAGSGGLLGDLPPPEPMAPMPVVAARAPSATRPSSGGKRSLLEDIPDAAPAPTAASAQAKARKPDTEALTAEYEKELRARLAREAAKTSFIARHGVKVAGAVVGVVVLAIVAISFINIRANQGGKTLSETLARAEDLIVQDTGASLDAALAQLQKARDMDDSSSRAWALTAWAHALRYADHGQASEDRRQALEALERPGVKDAAPALVLVTNVLVADERGRALARSALLGSQEESTEVHALAGSLLLEAKDEKQALERFDRALRASGVNVRALVALGGYYKASEDFPQAIEMYERARKRSPGHPGARIGQAEARLALYQDLDAALADVAPLAEDPKLPPSLKARQQLVHGELLSAQGKHAEARALLSKGTQGPLAFEFQLALGAASRAAGTLDAAQAAYEAALKLRPKSEEAREGLGRALLDRDREREVLSRLDADGGRKVSLVRGAAYARLGDWKKARAELARTRVNDRYPPEAVSWLALADAAEGNGAQARELLEKALQAAKRPRNDMRLALGQLYWRERAYDKAQSLFEEVQKDPRDHEGACSLGRLMLSRGLPDMALKPLTQAVERNGAHGEARDALGRTLLALGRTQDALKQFEAWQLENPGSAAAHKGFALALFHAGRRKDAEGAVQRSVKLASDDPEAHKLRAAILFGAGDARGGFSALARANKLDPKDADTFCEIALAFMRQGNSGNAEAAFAAARREGPDATCGRVGELYAQLPGGGRGAARTLEDLAARAPTVWDKAFARATMARALLGAGALKDARAAADEAVRLAPFDGRAQLALGMVALKQRQEAVARAALEKAVELEPADGLARLALADALVREPGELPRAVASYEAFLKLAGGANDAARVKKALPGLKKKAAR
>NZ_CP022203.1|WP_013938557.1|2363534_2363906_+|hypothetical-protein
MRYFSSRTDSPLLRIMWGNAFLLSLIYLLLGLGVEIALRFHPSSFLRRMSLSLDSLPARALELSGAMEPLRAAYFTGRISEWGVRVVFGLTTMAVIFVLAMVVGTLMGGVRTLLARRALRSRS
>NZ_CP022203.1|WP_095957944.1|2363902_2365984_-|ATP-dependent-DNA-helicase-RecQ
MMNMRAMPVDLPYLEEAQRGLVRHFGLSQFRPGQDQVISSVLSGRNTVVVMPTGAGKSLCYQLPATLLPGLTLVVSPLIALMKDQVEQLTARGIPATFINSSLSDLERAERMRKLRAREYKLLYVAPERFRSQSFLETVSAVGVDLLAVDEAHCISQWGHDFRPDYAQLGQVRKRLRPPRTVALTATATPEVRADIVRVLLMKDPQEFAMGFDRPNLFLGKQEVGGDADRHEACARLAATGGSGIVYCSTRRAAEGIFSELHGRGVKAVLYHAGMDDDARRRAQDTFMAAKEAVAVATNAFGMGIDKPDIRFVGHANIPRAVEAYYQEIGRAGRDGQAARAVLLFNHSDVFTQERLIQSSHPAEAIFGDVWNVLQSVEEFERGVHVLAGMVNASEFEVSAALRILEREGKVERGGRGEGEHGITLLEKATSAQPHSPDAQRLLKSLLETFPVGRQITTELPILARRIGLSVDEVRHALGLLEKAHVAKVRRPFAGRSIRALERLPFRELGLDLSRVREQERQNLSLLRRMTEYAYTDRDKKCRRSAILRYFGQRDAGTSCGNCDVCTPEKMPTLLAHGPAASRGRGPGSTAAPVVTNYSELASTELRRWRKELAKDLGVAPFIIFNDATLLGLSAALPVDREGFLAVKGTGESRWERFGPKVVEICLMARAAGHEPQAVPAAAARKPILRRRG
>NZ_CP022203.1|WP_013938559.1|2366029_2366281_-|hypothetical-protein
MVSVVGLWGAVQVELLEDTRAQVVRLDTGQACTVERASLPSGAREGDLVVDGRLEPGQTEARRRDVARIRARLAVPVPPGLDL
>NZ_CP022203.1|WP_095957945.1|2366280_2367051_-|DNA-repair-protein-RadC
MEQSAAGAAWAGDGSVSARGVGGAEESRERLFRLGAAALTDPELLCVVWSSGARAPGAWAVAGALLTEGGGLKGLVQQEPLALSLRPGVGPARAAQVLAALELGRRAQRAGERRPRLRTPKEIAAYLAPVLGALRREVFHVLCFNARNVLLHDARVAEGTMNTCPVDPREVFAAALTARATSIVLAHNHPSGDPEPSVQDLALTRHLVAGAQLLNIKVLDHVVVGDGGYVSMLERGLMPDEAKEQRRTWSANGGCG
>NZ_CP022203.1|WP_013938561.1|2367208_2367667_-|cyclic-nucleotide-binding-domain-containing-protein
MDADVLKKVALFEGLTQGQLAKVAQIGHSRTYPAGAFLFREGDAGQEMFVIAEGKVRISKSVPGVGEEALAVLEPGQYFGEMAVIEDSPRSADAIAHVSCAVWVIERSRLDQLMFTDKDLAYVLLWTFVRTLSERLRETNEKIKGFFALSRF
>NZ_CP022203.1|WP_013938562.1|2367739_2368702_+|thioredoxin-disulfide-reductase
MAEEKTNKVTIIGSGPAGYTAAIYAARANLQPVVFAGGPTLEHPQRVPGGQLMVTTDVENYPGFPEAITGPELMERFQKQAERFGTTIHMENVVKVDFSQRPFLIQGESVSYRSETVIISTGATAKWLGVKGEDTYKNRGVSACATCDGAFFKKQDVLVVGGGDTAMEEATYLAKIVNHVTLIHRRDTLRASKVMQERALQNPKISFMWDSAVEEVLGDNKGMNGAVVRNLKTGDSQLVKATGLFVAIGHTPNTELFQGVLETHQGGYLKTVPGSTRTNIEGVFACGDVQDHYYRQAITAAGTGCMAAIDAERWLIEHGE
>NZ_CP022203.1|WP_095957946.1|2368798_2369983_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MSSKQKTVAVHAGTRLAGSKAVPVSPPIYPAAVNWFDSSDDLDSALDGKDYAYARISAPNTTLLEEAVAALEGAEACVAYASGMAALRSVFEAQGFKPGDRLVMPADGYGVTRALYKRLCATLGVELHALLMTDPEVSARIRELKPRMVLAESISNPLLRVPDLRVLARACQDVGAAFVVDGTFPSPVGQRALALGADYAVQSTSKWLNGHSDALGGTVSASRERMAPLRAARVLAGDVLGPFEAWLTLRGLRTLPVRMKAHVEHAAHVARRLTESPLLERVIYPGLASHPDHATANALLLGGGPMVAFEIKGAGRAEGMRFLEALKVGRPGPSLGDVCTLVMHAASASARRFTPEERAAAGIQENLIRVSVGLEDPDDIADDLLAAVAQGARR
>NZ_CP022203.1|WP_095957947.1|2369979_2370474_+|cyclic-pyranopterin-monophosphate-synthase-MoaC
MKMVDVGEKPKTGRVAVATALLRMLPATRERILAGKVEKGDVLAAARLAGIMAAKRTPDFVPLCHPIALAGVEVTLAPEDAGLRVRAQVKTVDRTGVEMEALTAACAAALTVYDMCKSVDRGMVLDAVQLEHKSGGRSGTWQREEAAPAPQPAPRRRTRAKKAR

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Crispr_ID: NZ_CP022203_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_4

2964253-2964329

Orphan

Consensus_repeat	Method
GTGGATTCGACGTCACCGACGACGCC	CRISPRCasFinder

1 spacers

WYL

The CRISPR arrays of NZ_CP022203_4

>merge|NZ_CP022203|4|2964253-2964329|CRISPRCasFinder
GTGGATTCGACGTCACCGACGACGCCGATGCCCGGGTCGTTGGTCTCGCCGGTGGATTCGACGTCACCGACAACGCC

>NZ_CP022203|4|3|2964253-2964329|CRISPRCasFinder
GTGGATTCGACGTCACCGACGACGCC	GATGCCCGGGTCGTTGGTCTCGCCG
GTGGATTCGACGTCACCGACAACGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095958269.1\|2971233_2972271_-\|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl\|CDD\|225253
NZ_CP022203.1\|WP_095958265.1\|2961964_2963104_-\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP022203.1\|WP_095958267.1\|2965449_2967582_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|338048
NZ_CP022203.1\|WP_013939119.1\|2956240_2957281_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|227187
NZ_CP022203.1\|WP_095961569.1\|2967578_2968394_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP022203.1\|WP_095958262.1\|2951806_2953816_+\|adventurous-gliding-motility-protein-GltC	unknown	unknown	gnl\|CDD\|223021
NZ_CP022203.1\|WP_043710809.1\|2953909_2955196_+\|tetracycline-resistance-MFS-efflux-pump	unknown	unknown	gnl\|CDD\|340888
NZ_CP022203.1\|WP_013939131.1\|2974300_2975932_+\|RIP-metalloprotease-RseP	unknown	unknown	gnl\|CDD\|100084
NZ_CP022203.1\|WP_095958270.1\|2973385_2974216_+\|phosphatidate-cytidylyltransferase	unknown	unknown	gnl\|CDD\|366491
NZ_CP022203.1\|WP_095958272.1\|2977244_2978279_+\|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|237845
NZ_CP022203.1\|WP_095958271.1\|2976454_2977192_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB	unknown	unknown	gnl\|CDD\|274750
NZ_CP022203.1\|WP_013939121.1\|2959564_2960773_-\|DNA-polymerase-IV	unknown	unknown	gnl\|CDD\|176459
NZ_CP022203.1\|WP_043713020.1\|2972597_2973389_+\|isoprenyl-transferase	unknown	unknown	gnl\|CDD\|259850
NZ_CP022203.1\|WP_013939132.1\|2975939_2976443_+\|septal-ring-lytic-transglycosylase-RlpA-family-protein	unknown	unknown	gnl\|CDD\|223868
NZ_CP022203.1\|WP_095958264.1\|2961017_2961968_-\|RluA-family-pseudouridine-synthase	unknown	unknown	gnl\|CDD\|223638
NZ_CP022203.1\|WP_095958268.1\|2968633_2970970_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013939115.1\|2951039_2951810_+\|outer-membrane-beta-barrel-domain-containing-protein	unknown	unknown	gnl\|CDD\|275358
NZ_CP022203.1\|WP_095958261.1\|2950215_2951043_+\|outer-membrane-beta-barrel-domain-containing-protein	unknown	unknown	gnl\|CDD\|275358
NZ_CP022203.1\|WP_043713015.1\|2955206_2956244_+\|phosphate-acyltransferase-PlsX	unknown	unknown	gnl\|CDD\|235414
NZ_CP022203.1\|WP_095958263.1\|2957690_2959418_+\|polynucleotide-adenylyltransferase-PcnB	unknown	unknown	gnl\|CDD\|130997

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095958269.1\|2971233_2972271_-\|WYL-domain-containing-protein	gnl\|CDD\|225253	COG2378, COG2378, Predicted transcriptional regulator [Transcription].	2.73044e-41
NZ_CP022203.1\|WP_095958265.1\|2961964_2963104_-\|serine/threonine-protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	4.84924e-64
NZ_CP022203.1\|WP_095958267.1\|2965449_2967582_-\|hypothetical-protein	gnl\|CDD\|338048	pfam11617, Cu-binding_MopE, Putative metal-binding motif. The seqeunce of structure 2vov is not matched in any other sequence either in UniProt or in NCBI (Sep2014). The model is of a short repeat not found on the G1UBC6 - 2vov - protein. The presence of conserved cysteine residues and the lack of hydrophobic residues suggests that this repeat might be a metal-binding site, perhaps for zinc or calcium ions.	2.20322e-10
NZ_CP022203.1\|WP_013939119.1\|2956240_2957281_+\|hypothetical-protein	gnl\|CDD\|227187	COG4850, COG4850, Uncharacterized conserved protein [Function unknown].	4.30389e-05
NZ_CP022203.1\|WP_095961569.1\|2967578_2968394_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	0.0019757
NZ_CP022203.1\|WP_095958262.1\|2951806_2953816_+\|adventurous-gliding-motility-protein-GltC	gnl\|CDD\|223021	PHA03247, PHA03247, large tegument protein UL36; Provisional.	8.07198e-06
NZ_CP022203.1\|WP_043710809.1\|2953909_2955196_+\|tetracycline-resistance-MFS-efflux-pump	gnl\|CDD\|340888	cd17330, MFS_SLC46_TetA_like, Eukaryotic Solute carrier 46 (SLC46) family, Bacterial Tetracycline resistance proteins, and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of the eukaryotic proteins MFSD9, MFSD10, MFSD14, and SLC46 family proteins, as well as bacterial multidrug resistance (MDR) transporters such as tetracycline resistance protein TetA and multidrug resistance protein MdtG. MDR transporters are drug/H+ antiporters (DHA) that mediate the efflux of a variety of drugs and toxic compounds, and confer resistance to these compounds. TetA proteins confer resistance to tetracycline while MdtG confers resistance to fosfomycin and deoxycholate. The Solute carrier 46 (SLC46) family is composed of three vertebrate members (SLC46A1, SLC46A2, and SLC46A3), the best-studied of which is SLC46A1, which functions both as an intestinal proton-coupled high-affinity folate transporter involved in the absorption of folates and as an intestinal heme transporter which mediates heme uptake. MFSD10 facilitates the uptake of organic anions such as some non-steroidal anti-inflammatory drugs (NSAIDs) and confers resistance to such NSAIDs. The SLC46/TetA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	3.99731e-72
NZ_CP022203.1\|WP_013939131.1\|2974300_2975932_+\|RIP-metalloprotease-RseP	gnl\|CDD\|100084	cd06163, S2P-M50_PDZ_RseP-like, RseP-like Site-2 proteases (S2P), zinc metalloproteases (MEROPS family M50A), cleave transmembrane domains of substrate proteins, regulating intramembrane proteolysis (RIP) of diverse signal transduction mechanisms. In Escherichia coli, the S2P homolog RseP is involved in the sigmaE pathway of extracytoplasmic stress responses. Also included in this group are such homologs as Bacillus subtilis YluC, Mycobacterium tuberculosis Rv2869c S2P, and Bordetella bronchiseptica HurP. Rv2869c S2P appears to have a role in the regulation of prokaryotic lipid biosynthesis and membrane composition and YluC of Bacillus has a role in transducing membrane stress. This group includes bacterial and eukaryotic S2P/M50s homologs with either one or two PDZ domains present. PDZ domains are believed to have a regulatory role. The RseP PDZ domain is required for the inhibitory reaction that prevents cleavage of its substrate, RseA.	3.54228e-56
NZ_CP022203.1\|WP_095958270.1\|2973385_2974216_+\|phosphatidate-cytidylyltransferase	gnl\|CDD\|366491	pfam01148, CTP_transf_1, Cytidylyltransferase family. The members of this family are integral membrane protein cytidylyltransferases. The family includes phosphatidate cytidylyltransferase EC:2.7.7.41 as well as Sec59 from yeast. Sec59 is a dolichol kinase EC:2.7.1.108.	4.20628e-55
NZ_CP022203.1\|WP_095958272.1\|2977244_2978279_+\|aspartate-semialdehyde-dehydrogenase	gnl\|CDD\|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	6.11135e-76
NZ_CP022203.1\|WP_095958271.1\|2976454_2977192_+\|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB	gnl\|CDD\|274750	TIGR03725, T6A_YeaZ, tRNA threonylcarbamoyl adenosine modification protein YeaZ. This family describes a protein family, YeaZ, now associated with the threonylcarbamoyl adenosine (t6A) tRNA modification. Members of this family may occur as fusions with ygjD (previously gcp) or the ribosomal protein N-acetyltransferase rimI, and is frequently encoded next to rimI. [Protein synthesis, tRNA and rRNA base modification].	9.16229e-42
NZ_CP022203.1\|WP_013939121.1\|2959564_2960773_-\|DNA-polymerase-IV	gnl\|CDD\|176459	cd03586, PolY_Pol_IV_kappa, DNA Polymerase IV/Kappa. Pol IV, also known as Pol kappa, DinB, and Dpo4, is a translesion synthesis (TLS) polymerase. Translesion synthesis is a process that allows the bypass of a variety of DNA lesions. TLS polymerases lack proofreading activity and have low fidelity and low processivity. They use damaged DNA as templates and insert nucleotides opposite the lesions. Known primarily as Pol IV in prokaryotes and Pol kappa in eukaryotes, this polymerase has a propensity for generating frameshift mutations. The eukaryotic Pol kappa differs from Pol IV and Dpo4 by an N-terminal extension of ~75 residues known as the "N-clasp" region. The structure of Pol kappa shows DNA that is almost totally encircled by Pol kappa, with the N-clasp region augmenting the interactions between DNA and the polymerase. Pol kappa is more resistant than Pol eta and Pol iota to bulky guanine adducts and is efficient at catalyzing the incorporation of dCTP. Bacterial pol IV has a higher error rate than other Y-family polymerases.	3.902e-169
NZ_CP022203.1\|WP_043713020.1\|2972597_2973389_+\|isoprenyl-transferase	gnl\|CDD\|259850	cd00475, Cis_IPPS, Cis (Z)-Isoprenyl Diphosphate Synthases. Cis (Z)-Isoprenyl Diphosphate Synthases (cis-IPPS) catalyze the successive 1'-4 condensation of the isopentenyl diphosphate (IPP) molecule to trans,trans-farnesyl diphosphate (FPP) or to cis,trans-FPP to form long-chain polyprenyl diphosphates. A few can also catalyze the condensation of IPP to trans-geranyl diphosphate to form the short-chain cis,trans- FPP. In prokaryotes, the cis-IPPS, undecaprenyl diphosphate synthase (UPP synthase), catalyzes the formation of the carrier lipid UPP in bacterial cell wall peptidoglycan biosynthesis. Similarly, in eukaryotes, the cis-IPPS, dehydrodolichyl diphosphate (dedol-PP) synthase catalyzes the formation of the polyisoprenoid glycosyl carrier lipid dolichyl monophosphate. cis-IPPS form homodimers and are mechanistically and structurally distinct from trans-IPPS, which lack the DDXXD motifs, yet require Mg2+ for activity.	1.7945e-121
NZ_CP022203.1\|WP_013939132.1\|2975939_2976443_+\|septal-ring-lytic-transglycosylase-RlpA-family-protein	gnl\|CDD\|223868	COG0797, RlpA, Lipoproteins [Cell envelope biogenesis, outer membrane].	3.95453e-47
NZ_CP022203.1\|WP_095958264.1\|2961017_2961968_-\|RluA-family-pseudouridine-synthase	gnl\|CDD\|223638	COG0564, RluA, Pseudouridylate synthases, 23S RNA-specific [Translation, ribosomal structure and biogenesis].	9.97211e-81
NZ_CP022203.1\|WP_013939115.1\|2951039_2951810_+\|outer-membrane-beta-barrel-domain-containing-protein	gnl\|CDD\|275358	TIGR04565, hypothetical_protein_N47_G32130, outer membrane beta-barrel protein. Members of this family are outer membrane beta-barrel proteins, as inferred by distant homologies to other families (e.g. pfam13505) and by the concentration of aromatic residues, especially Phe, in the OMP signal region, which is flush with the C-terminus in some members, but followed by a few residues in others. Members have variable insertions and deletions, affecting scores, so this model does not cleanly separate all members from all non-members. Members are common in the Myxococcales, with five occurring in Myxococcus xanthus DK 1622.	4.93266e-40
NZ_CP022203.1\|WP_095958261.1\|2950215_2951043_+\|outer-membrane-beta-barrel-domain-containing-protein	gnl\|CDD\|275358	TIGR04565, hypothetical_protein_N47_G32130, outer membrane beta-barrel protein. Members of this family are outer membrane beta-barrel proteins, as inferred by distant homologies to other families (e.g. pfam13505) and by the concentration of aromatic residues, especially Phe, in the OMP signal region, which is flush with the C-terminus in some members, but followed by a few residues in others. Members have variable insertions and deletions, affecting scores, so this model does not cleanly separate all members from all non-members. Members are common in the Myxococcales, with five occurring in Myxococcus xanthus DK 1622.	2.05529e-37
NZ_CP022203.1\|WP_043713015.1\|2955206_2956244_+\|phosphate-acyltransferase-PlsX	gnl\|CDD\|235414	PRK05331, PRK05331, phosphate acyltransferase PlsX.	2.14758e-124
NZ_CP022203.1\|WP_095958263.1\|2957690_2959418_+\|polynucleotide-adenylyltransferase-PcnB	gnl\|CDD\|130997	TIGR01942, pcnB, poly(A) polymerase. This model describes the pcnB family of poly(A) polymerases (also known as plasmid copy number protein). These enzymes sequentially add adenosine nucleotides to the 3' end of RNAs, targeting them for degradation by the cell. This was originally described for anti-sense RNAs, but was later demonstrated for mRNAs as well. Members of this family are as yet limited to the gamma- and beta-proteobacteria, with putative members in the Chlamydiacae and spirochetes. This family has homology to tRNA nucleotidyltransferase (cca).	1.0731e-91

>NZ_CP022203.1|WP_095958265.1|2961964_2963104_-|serine/threonine-protein-kinase
MPPKVIGPYRVLETLGSGGAGTVYRALDRRTTDEVALKLLSAGPARDARAARRLAREFDTLVDLSHPNVVKVFESGVHQGVPYLAMELIEGLTLRHYLDLGSGERPPHPGSHTPRSPLSVLRTADDDFGPLNRDFSDSMDDSDASPHEGTFGLEAFAEEAPSEDLESFASGFSPHAGIGSDDSMEGFDLVPPLPRTLPPEEPDRLLRAEDLNRPERMGRLKDAMLQICEALAYIHGHGLVHRDLKPSNIMVDDDRQVRLMDFGLAKFLADDAAITEAGKLVGTYRYMAPEQILGEPLDGRSDLYSLGVILYELLSGRPPFDAKTPHELWRQVLETEPPPVLALNLHGDPQLARVAHRLIRKEPDDRFQTAEEVYEALSE
>NZ_CP022203.1|WP_095958264.1|2961017_2961968_-|RluA-family-pseudouridine-synthase
MNPSKLHTLTVDADKAGQRVDLFVGEALGLSRARLKRLFEAGAVKVNGRPAKKGLTLTAGQHIAVEVEEESREAVPDADFPLTVLHEDDSLVFVDKPAGRPSHPLQSGETGTVANALVARYPECAQASVDAREGGLCHRLDVETSGVVVAARTRDAWNAVREAFGGRAVDKRYLALVTGPLADEGDIDLPLRHHPRHPDRVEPAPSGAADAREAVSKFTVLSRSGEFSVVEVKILTGVLHQVRAHLAGVGAPIVGDSLYGGREAPELGRFFLHARSLGLTHPQTKRAMTVHSPLPPELRAELERHGLPLPRGEQRS
>NZ_CP022203.1|WP_013939121.1|2959564_2960773_-|DNA-polymerase-IV
MRAIIHVDMDAFYASVEQRDNPALRGKPLIVGGHAQRGVVVAASYEVRPFGVRSAMPMARAMKAAPHALVVKPRFSAYAEASEHVFAIFERYTPLIEPLSLDEAFLDVTASVGLFGTPADIARRIRKEIADELGLPSSAGVATVKFVAKIASDLAKPNGQREVRAEETVAFLAGLPVSRLWGVGPKTEEALRLAGLKTIGDVAARELDWLEDRLGSSGRHLWELSQGIDTREVVPDRAAKSVGAEDTFDEDLVGMDALKPHVHAQALRVARRLRRAALKGRVVQLKLKFADFTLITRRTTLREATDDGQTLYRAALELMEKAHQGKPLRLTGVSVQLDEEQPQLGLFPAAAPRTAKLNAALDKIAERFGSKAITTADIAGSEATDSAEHRSERPVDKGGPKS
>NZ_CP022203.1|WP_095958263.1|2957690_2959418_+|polynucleotide-adenylyltransferase-PcnB
MNSNLELSAPPEEDSAAKPVAADEQAATETPTIQTAPASVPAPEPASPPARADAEDEDDEEEDDDEADPAEAGLDEAVLGAEAALAAAEAEDAAEARGEEVEEVPTILEPEPEPTPDERALHAPHVRPTGEPAEIDPDELDPDALKVVLRLHQHGHQAYMVGGCVRDLLLGRKPKDFDIATSATPNEVRGIFRNCRLIGRRFRLAHVYFKGGKIIEVSTFRANPTELEAAANGGEDDGEGEDLLITHDNVFGTAQQDARRRDFTINGLFYDVAEGRVIDYVRGRRDLDERFIRTIGDPEVRMREDPVRILRAVRFAAKLELDIESRTYAAMEGAVEDLPRCAPARLLEETFRLIRGGVSAPALKLLDALDALKILLPPVNAYLKQHGKEGEKTFYAFAEALDRRVSAGEPLDDAILLAMLLIPISRSTGPEESQDGGRPSVSQVVEDLLADFVQSARLPRRIAERCRMLLLAQRTLTGERRRRSAAFKRHPLFSEALTVFEMTVEATGENREQLEAWKAGEVPQPRAAAADGEESDAGGQRKRRRRRRRRRPSANGGSGEGAGSSSESGSDAGDA
>NZ_CP022203.1|WP_013939119.1|2956240_2957281_+|hypothetical-protein
MSLPDRIDPRPPRRIYRWDLDKTYLQTEFDSLRDLVRTAFQKAHQKVAVPGASALIRELSENGDSRLCIVSGSPKQMRAVLEEKLKLDGVRWDEFVLKDNVGNLLRGRFRALRGQVGYKLPAILESRVHAPVEAEEVLFGDDAEADAFIYSLFADLVAGRVDERVLSQVLEAGGVYPDDAERVREAWKKIPVGDPVRRIFIHLDRLTPPAHFTPYGPRVVPIFNYFQAALVLLADGHLTAPQVLKIAVEMVQTAGHNIITLSNSFQDLLRRGLPLQQAAVALSQALEGPNKLLAAMRPMPDILAAFSKRLAALGTPPPPPPVQAVDYVSLIHHALPRNHKGRSKPQ
>NZ_CP022203.1|WP_043713015.1|2955206_2956244_+|phosphate-acyltransferase-PlsX
MVGTQPQPVTIAFDVMGTDHGPAEVVRGAAMLSLESPHIHTLLVGDRTLIDDALAETKHNGERISVQHAADFIGMDEKPGEALARKPNASVAVAARLVAEGEAQALVSAGNTGAGVLACARHFQLIPGVRRAALATVYPTRSVRGAKGDPFSLILDVGATVEATADDLVTFAVMGSAYARIISQNERPKVALLSNGIEPQKGPPRVVEAHARLSEMKDIHFIGNVEGIDIPKGTADVIVTDGFVGNVCLKMLEGVHDTVVELAQYAYKESLRWRAGLAMLSSGIQRIKDITDWNQYGGAPILGFDKIFIKAHGRSKSRAIANAGKVAAKVVSNNLGAAIREGLKT
>NZ_CP022203.1|WP_043710809.1|2953909_2955196_+|tetracycline-resistance-MFS-efflux-pump
MVRRAASLRVVFGIVALDLIGFGILIPQLGVYGVRFGASPFTVGLLISIYSLMQLVSAPVLGRLSDRYGRRPVLLVSQVGSLLAYLLFAFAQSLPLLFLARVIDGISGGNISTAQAVVADITPPKDRARGMGVIGAAFGLGFVLGPALGGFLGAWGGNLAIGLFAAGLVALNLTSTYFFLPETRVEGRPGEGHARTLKGATLAMNLPVVGRCLVLMLVFTTAFAQMEGTFSVYLLTRFLSSGPVPLQDGGLFLRAAVTDLDVLREASLRSGWLFAAVGVISAAVQGGLVRRLTGGPGSRPGREALLATAGFGLTAAGLGLLPVAPDYAWLFPVMGLLAVGSALVTPCLSALVSLHAPPERLGAVLGAYQAFGSLGRILGPALGGWLFTRLGPAAPYGTAAGMVALSGLLGLALVAQARMAGAGAEQRS
>NZ_CP022203.1|WP_095958262.1|2951806_2953816_+|adventurous-gliding-motility-protein-GltC
MMRSFRLIRVAVVGLSLAWTAPTFAQSFEGLDLSGQSKKKKRPTKKKKRPTRKARTDKAKPAPVQDEAGDDDAAASSIEAPTTVAPAEAAPAPAPTPASPPANTGSMGMGLDLTQEAPKPAAPTMSFDAVDVSGKTADRQRLDVAVSLFKNDEYEKASMAAHELLEDPKLAGLHTEARYVLAKSLYRMGMYHSSLGEFSKILSLGPSTKFFKTSLEWLFFISRKTKNETVILDEIARHANQEFPEKYRNEFRYLLARYHFVRGRALDQVGQPEEADKSFSEVKRLALTIPRTDPFFPRAKYLEGLSSFRNGSRQKDAAAKRANGEMLAAIEAMKEVVRLTRPVAGKTPEQAKADKSLRELAFMQLARTHYGMQQNRFALFYLGKVERGNTQWLESLFESAWANYRVGQYEQALGNLITLSSPFFREEYFPEALILKAVIYYENCRYRESTSILGDFERTYLPVHDQLEALVKKNMEASEYYSVLADVQKKNKEGLEKNETDLILERILRLALTDQDLRKTNDSILELEAEMDAFANRADTFKYSELSKSLLDGLKVQRTALISKAGIMAKGKLETELVALKQLLANGLRIKFETTTKEKEFLEEQLKAGGRTAIVKKYKYSVAVQDDQLYWPYEGEYWRDELGTYQYTMTKGCIERDTANRNVQSAEAM
>NZ_CP022203.1|WP_013939115.1|2951039_2951810_+|outer-membrane-beta-barrel-domain-containing-protein
MKRLFRVLLALCLTGPALGSAQTTEEVEAGDVSEVDKDRLGPLRERVRPVSGHVFLKKGRLEFSPSATLSLRDAFYSKYIFGGTLTYHPMETLGISLRVGYAVNTVAGAAQKCTFGDGGEGSTRGCVAPTLNELDGNAPGQIKLLGGADVQWAPIYGKVSLLAETFVHFDLYGVAGASLVQYRGPGETPGTVAQNYLTPGANLGVGARFFLNRWVTLRTELRDLIYVEKGTEVSGNYLRNQLLFELGVSFFFGSES
>NZ_CP022203.1|WP_095958261.1|2950215_2951043_+|outer-membrane-beta-barrel-domain-containing-protein
MNRPKLLLALCLVPALASAQSQEGMGLDLTDESQAESSQDAESPAPPPVEEASPAAASSLADEPVEEDPQLPLTDITQEDRVKSVQRKVYLKKGRFELTPLLSFSVNDAFYSKVGLSVRGAYYLADTLAISARGSLMQVVPSDDVRTAKRTFNSQIYYSVPQWSAMGDVEWSPIYGKVAFLNSILHFDGYLLAGAGVVRTETSALPGRGLNPAADLGLGMRFVAQDYLAVNVALINTSYVDQPLGSSKGAIQNVMTLNAGISLFLPFKSTGRDSE
>NZ_CP022203.1|WP_095958267.1|2965449_2967582_-|hypothetical-protein
MNRLYLACLVLSGMACTVPSLDELHPCDLPSLIGAPVDAVLGDQPTCRVIQVKIHAAGFRPGCVRVGAHDEASEQALTAELSGEDVPSGDLLAISVVVPKDWDDAVQVEARAFEQSCNAAPVATHAVRLPGVKEGVTRVELDLRATDADGDGYVAVLTGGTDCDDDTPDIHPGATERCNDVDDNCNGVSDEVELSLGQHCTEAAGCEGTRTCDVNGTVVCSMPLAVYASPDVDQDGHGDRSVTPVAFCAGVPPGYVVSPADDCNDNNASIRPGATELCNGVDDNCNDQIDEAFPELNTACTAAAQCAGVYVCDASGIATTCQATQTSTHWYLDDDGDGFGVDTAVSSCVSPGARYVTSSGDCNDGNPFTHPGAPELCDGLDNDCDGSTEGPAACPGSAGNWVPRTVGAATQEWRSIFTEVPGDVTVVGNQGGTAVLAPGATSFQTNASNCGNSTRGWNAVWTDMSNQGRAYIGSSAGSLSFLDRAQNACTETHNFGRWVRGLIGIRHEGTLEIHGVTSTSGTVNQGLTFIWNGTSGAAALNFGNNPVAHLYDIHGRSRSALFAVGGVETGSSQGRIYRFNSLIPQWEVGLLQDAIPGLGRLRGVWVVSDDLAFAVGEALDGMNTVLRWNGSTWSRMPFPTTHIETLTSVVAFGANSVYVTAYDGRIYRYDVTGWQIIYENTAIRLNDIAGTSPADLWVAGSNGQILHWPQ
>NZ_CP022203.1|WP_095961569.1|2967578_2968394_-|tetratricopeptide-repeat-protein
MLSHALLLPGLAFGQSVTSKAAQAGTRDSAFRSRLKAAAQLYEELEYESALKALTRAKAIATTDAERADAAMYEAIVLADLGKRSQSLRAFREALLLEPESQLPVRVSPKVARDFDEVRKRVQSERVAVSPVAPTSPATSQDRPVLEPETEASAVALSTHPAPTAPLIAAPEDRLVTTEQGGLRIRPLPVALLGAGVLAGGIGSYFGLSSRSDIQSARDTFDVEEQMGHLDSARGKALGANILFGVAATAAAGAVITYLLGDGATSQREAP
>NZ_CP022203.1|WP_095958268.1|2968633_2970970_-|hypothetical-protein
MDAGSDDAGVPDAGDNEPDAGSGDGGEPDAGTSCEPSSVTDLLDNGEWDPRFSIGGVSGMDGHVPHIYDLAKTPSGDLLATGYFRWFGAQASTPLIRHQDGQWRPEPRTWSQEIPGGAGFSAVAAKDDTTLALATNDTFGDRGGEVWIQSPDGVQVIGHFTGLVRTMAYVRDELWVAGQFQLEENGAIGLAIWDGTAWKLPPGGPADGSVYELMLQGDDVWVGGAFTRVGGISSNKVAKWNGSRWESYNFPIAGNGVYALTLGDDGTLYAGGTFAYDFNADGVGSIARWNGVRWEMLDGGVSTGFYPGVVTDLVFNQGKLHVGGCFNFVNGQGYGNPLALQANALALWSPESGWENWPQAISPNRTVWYAPSFCGDEPPVTFAVWEVPIQRFLLDGDRIYVAGTLPSIDGAASQSIVSYEGGQWRAEGAEPGHGLSGGAQMLAVGGEQCTVHALGDISHAGGAAVPRTVLQFTDAGWQALGELPDMECLDLAVNAQGDIYVACIDWDSVQSQLLTWSGTEWTSLGDLSAHGFISKLTLDSLGRPWLTSMVESTSRVVRWTGTQFELVADGLDGPVFALALRPENDDPDRPAFVVAGEFTHAGEVPARRIAHWNGTTFEALGDGLTTSPITAAYGPNGIFASTNHEQDMDGNPVQGRLMLGHWDGTAWRELATPENGMPGPLNEEQGGVHSFRKLAFAGTDLVVVGTIFPADGGPTHAYVFNGERFLPIGGGVSALTMDDIALTPDGIWLGGNIAEAGRGENLLPTVGMAHFRRRAAAP
>NZ_CP022203.1|WP_095958269.1|2971233_2972271_-|WYL-domain-containing-protein
MRADRLVSLTLLLQTRPKMTAGELARELQVSERTIHRDLDALSGAGVPVYATRGAAGGVALMEGWRTQLTGFTRTELHALAAVAAPGALDDLGLTSALRSGLVKLAASLPALQQPALEYARQRLHVDASSWFAEREPVPHLATLRDAVWQDRRVSLTYRDFEGTPSRKVVDPYALVIKADRWYLVARTGADEPRVYRGSRVEGARLRPETFVRQARFDLPAFWKAWCARFAEKRARYEVTLRLTPEALEALRKIRPRAEGARLAAAPPEADGHKTVIVDFERESIAFSQLCDVGAGFEVLAPEFLRMRLMKLATSLLDSHGDDAAKRASARHTRARARAHPPSDY
>NZ_CP022203.1|WP_043713020.1|2972597_2973389_+|isoprenyl-transferase
MERPSVISTLEQAVKARPMPRHVGIIMDGNGRWAESRGLPRLEGHREATSSVREVTRTARRLGIQALTLYAFSSQNWARPAEEVAGLMELLREYLERERAEILDNGIRLNAIGDVDRLPRYVREPLDRLRADSAHNTGMVLSLALSYGGREEILQAARRLAEAVERGELAAGRLEESDFEQFLWTQGLPPLDLMVRTSGELRVSNFLLWQMAYAEMCFTDALWPDFRTDEFLRCVSQYQQRERRFGLTSAQVQREDAPQQAKA
>NZ_CP022203.1|WP_095958270.1|2973385_2974216_+|phosphatidate-cytidylyltransferase
MNDKNRNLVIRVVSAVTLLPLVILLLFLGGYWSAALLGAAAAACVGEYYLIVQKRLTVASWVGLAFAAVMPFLPLRDAARTGETAFWLTVVFAFFAWIYHLFKGPLAEAPTRTAHLVNGFLYGAVGLTAMSALRLLPDHGMAWVICALVITWANDTAAYFFGRFLGKHKLYPEVSPNKTWEGFFGGMLGSVGGMFIARQFFFPVFTVWDCVLLGIAGGILGPVGDLCESMLKRAYGVKDSGFLIPGHGGVLDRIDALLFNAPLVFVYVQFVRDLLP
>NZ_CP022203.1|WP_013939131.1|2974300_2975932_+|RIP-metalloprotease-RseP
MLQNIGFFVILLGVLVTVHELGHFLVAKACGVKVLKFSIGFGPKLIGFTKGETEYQIALLPLGGYVKMAGDMPHEELSPEEASRGFLAQPPWKRGLIVLAGPAFNLIFPILVYFFVFLGPHQATSTYVGSVSEGMPAQAAGIRPGDRILSVDGEPVRTFNDMREAFVGRFERPIPIGLERNGQKLTLDVTPTKQVETSPIDTVERGSIGVEAVSKPPIMGVPPGSVAEQAGLRTFDRILAVNGVSVETEARFQQELDKHAEGAPLELTLRRMEPVAAGAVTGRVPSVLKLTVPKQPGEGLAAVGAETSDLYLATVAPGSAAEKGGLRPGDRIIALDGEKPESFVKFSSKLNALKERSFQLTWRGADGERTKTLAQAPLKTEDELGTATSPIVLGVRPWVLSAADMPVLDEVTVHLGPGDALKQAALIVPKIVGQMVRVLGGLVTGSVPMNTVGGPIMMYQLASKSAEQGLDSFLHLMALISINLGVMNLLPIPVLDGFHLLSAAWEGIRRRPIPVRVREVANMVGLALLVLLMLLAVTNDITR
>NZ_CP022203.1|WP_013939132.1|2975939_2976443_+|septal-ring-lytic-transglycosylase-RlpA-family-protein
MRGFAVAGLLCLGFTSACASRAAKPDPVEAPPRSSKSPKPRGGAPGVTKRPKMPRSYLGEGLASFYGPGLHGRPTASGERFDQEAMTAAHRKLRFGSCLRVVNMENGRAVKVRVNDRGPFIDGRIVDLSKGAARKLDMLDKGVVRVRLYRCDDRLSEIPQAMWAAPV
>NZ_CP022203.1|WP_095958271.1|2976454_2977192_+|tRNA-(adenosine(37)-N6)-threonylcarbamoyltransferase-complex-dimerization-subunit-type-1-TsaB
MFLALDTSTLTLSLALVERAPDGAPRTLEHVVVGPPRKQSELLPGIVGELLARHGATLPGLEGLVVGLGPGSFTGLRIGLATAKSLAYAAKLKVAGASSLAAVALEGPEDVPLYCLAVARKDDLYLGAYVRRGGAVEPLAPETAMSPAEVAARMAAEPRAVALGPALVDYRAALESHGVAPHRLLAAPAFPSAVALARLARFPETQTLEALFAMEPHYVRASEPERNPKFPPLPGPAPTARLKED
>NZ_CP022203.1|WP_095958272.1|2977244_2978279_+|aspartate-semialdehyde-dehydrogenase
MRDDLTIGVVGATGVVGREVLAALYAQDVPAEQVRVFGSERSKGMEVEYGEDSLEVEHATPDAFRGVKLVLLATPAEASRTLAAAAQAAGAWVVDASNAFRGDGNVPMVLPGFNADVLGAGFTFKGRIVCLPGAVTTAAVHVVEPLRKAFGVTRAQVTALMAASSAGVRGVAELEKQTADLLSGREPEPHAFPHRVGFNLVPQVGGFMVNSPWTEEEGGWTLEAARLFSSKGDVPVIAGTAVQVPTFYGHGLTLNVQLKKPGPVEQVRAALKTSGALKVLDVPGERVYPMPMLVTSDPAVHVGRVRAFPQAPEWVTLFASVDNASRGAALNLVEAGFRLAERPA

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Crispr_ID: NZ_CP022203_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_5

3443659-3443773

Orphan

Consensus_repeat	Method
GGTGGGCTCGCGCCCGCCTTTCGTGCAGGGCGGCCCCGCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022203_5

>merge|NZ_CP022203|5|3443659-3443773|CRISPRCasFinder
GGTGGGCTCGCGCCCGCCTTTCGTGCAGGGCGGCCCCGCGACGTCCGGGCCTCACGGGGGTGTGCCGCCCGGGATGGTGGGCTCGCGCCCGCCTTCCGTGCAGGGCGGCCCCGCG

>NZ_CP022203|5|4|3443659-3443773|CRISPRCasFinder
GGTGGGCTCGCGCCCGCCTTTCGTGCAGGGCGGCCCCGCG	ACGTCCGGGCCTCACGGGGGTGTGCCGCCCGGGAT
GGTGGGCTCGCGCCCGCCTTCCGTGCAGGGCGGCCCCGCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095958529.1\|3456719_3457628_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP022203.1\|WP_095958531.1\|3460905_3461514_-\|winged-helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|379282
NZ_CP022203.1\|WP_095958516.1\|3427633_3430462_+\|zinc-ribbon-domain-containing-protein	unknown	unknown	gnl\|CDD\|274350
NZ_CP022203.1\|WP_157757504.1\|3460471_3460990_-\|transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP022203.1\|WP_013939498.1\|3437844_3439239_+\|undecaprenyl-phosphate-glucose-phosphotransferase	unknown	unknown	gnl\|CDD\|274396
NZ_CP022203.1\|WP_095958517.1\|3430463_3431729_+\|phosphoribosylamine--glycine-ligase	unknown	unknown	gnl\|CDD\|234856
NZ_CP022203.1\|WP_095958522.1\|3439308_3441249_-\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379142
NZ_CP022203.1\|WP_157757502.1\|3436481_3437591_+\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340833
NZ_CP022203.1\|WP_095958519.1\|3432834_3433950_+\|YjgP/YjgQ-family-permease	unknown	unknown	gnl\|CDD\|367632
NZ_CP022203.1\|WP_095958527.1\|3454885_3456085_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095958521.1\|3435273_3436395_-\|glycosyltransferase-family-4-protein	unknown	unknown	gnl\|CDD\|340838
NZ_CP022203.1\|WP_157757503.1\|3456081_3456723_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP022203.1\|WP_095958532.1\|3461556_3463029_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095958515.1\|3426085_3427630_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	unknown	unknown	gnl\|CDD\|234854
NZ_CP022203.1\|WP_095958525.1\|3452495_3452837_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	unknown	unknown	gnl\|CDD\|239278
NZ_CP022203.1\|WP_095958526.1\|3452992_3454792_+\|glycosyl-hydrolase	unknown	unknown	gnl\|CDD\|119365
NZ_CP022203.1\|WP_095958520.1\|3433951_3435322_+\|O-antigen-ligase-family-protein	unknown	unknown	gnl\|CDD\|377422
NZ_CP022203.1\|WP_095958518.1\|3431725_3432838_+\|YjgP/YjgQ-family-permease	unknown	unknown	gnl\|CDD\|367632
NZ_CP022203.1\|WP_095958524.1\|3449109_3451890_-\|vitamin-B12-dependent-ribonucleotide-reductase	unknown	unknown	gnl\|CDD\|235828
NZ_CP022203.1\|WP_043713138.1\|3459038_3460346_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|275097

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095958529.1\|3456719_3457628_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	3.65073e-06
NZ_CP022203.1\|WP_095958531.1\|3460905_3461514_-\|winged-helix-turn-helix-domain-containing-protein	gnl\|CDD\|379282	pfam13592, HTH_33, Winged helix-turn helix. This helix-turn-helix domain is often found in transferases and is likely to be DNA-binding.	3.83486e-15
NZ_CP022203.1\|WP_095958516.1\|3427633_3430462_+\|zinc-ribbon-domain-containing-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.	1.74073e-18
NZ_CP022203.1\|WP_157757504.1\|3460471_3460990_-\|transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain 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.	4.05018e-23
NZ_CP022203.1\|WP_013939498.1\|3437844_3439239_+\|undecaprenyl-phosphate-glucose-phosphotransferase	gnl\|CDD\|274396	TIGR03023, Sugar_transferase., Undecaprenyl-phosphate glucose phosphotransferase. This family of proteins encompasses the E. coli WcaJ protein involved in colanic acid biosynthesis, the Methylobacillus EpsB protein involved in methanolan biosynthesis, as well as the GumD protein involved in the biosynthesis of xanthan. All of these are closely related to the well-characterized WbaP (formerly RfbP) protein, which is the first enzyme in O-antigen biosynthesis in Salmonella typhimurium. The enzyme transfers galactose from UDP-galactose (NOTE: not glucose) to a polyprenyl carrier (utilizing the highly conserved C-terminal sugar transferase domain, pfam02397) a reaction which takes place at the cytoplasmic face of the inner membrane. The N-terminal hydrophobic domain is then believed to facilitate the "flippase" function of transferring the liposaccharide unit from the cytoplasmic face to the periplasmic face of the inner membrane. Most of these genes are found within large operons dedicated to the production of complex exopolysaccharides such as the enterobacterial O-antigen. Colanic acid biosynthesis utilizes a glucose-undecaprenyl carrier, knockout of EpsB abolishes incorporation of UDP-glucose into the lipid phase, and the C-terminal portion of GumD has been shown to be responsible for the glucosyl-1-transferase activity.	0
NZ_CP022203.1\|WP_095958517.1\|3430463_3431729_+\|phosphoribosylamine--glycine-ligase	gnl\|CDD\|234856	PRK00885, PRK00885, phosphoribosylamine--glycine ligase; Provisional.	0
NZ_CP022203.1\|WP_095958522.1\|3439308_3441249_-\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	3.58241e-16
NZ_CP022203.1\|WP_157757502.1\|3436481_3437591_+\|glycosyltransferase	gnl\|CDD\|340833	cd03804, GT4_WbaZ-like, mannosyltransferase WbaZ and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. WbaZ in Salmonella enterica has been shown to possess mannosyltransferase activity.	9.24248e-146
NZ_CP022203.1\|WP_095958519.1\|3432834_3433950_+\|YjgP/YjgQ-family-permease	gnl\|CDD\|367632	pfam03739, YjgP_YjgQ, Predicted permease YjgP/YjgQ family. Members of this family are predicted integral membrane proteins of unknown function. They are about 350 amino acids long and contain about 6 transmembrane regions. They are predicted to be permeases although there is no verification of this.	2.43064e-64
NZ_CP022203.1\|WP_095958521.1\|3435273_3436395_-\|glycosyltransferase-family-4-protein	gnl\|CDD\|340838	cd03809, GT4_MtfB-like, glycosyltransferases MtfB, WbpX, and similar proteins. This family is most closely related to the GT4 family of glycosyltransferases. MtfB (mannosyltransferase B) in E. coli has been shown to direct the growth of the O9-specific polysaccharide chain. It transfers two mannoses into the position 3 of the previously synthesized polysaccharide.	1.31775e-81
NZ_CP022203.1\|WP_157757503.1\|3456081_3456723_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274357	TIGR02937, RNA_polymerase_sigma_factor, RNA polymerase sigma factor, sigma-70 family. This model encompasses all varieties of the sigma-70 type sigma factors including the ECF subfamily. A number of sigma factors have names with a different number than 70 (i.e. sigma-38), but in fact, all except for the Sigma-54 family (TIGR02395) are included within this family. Several Pfam models hit segments of these sequences including Sigma-70 region 2 (pfam04542) and Sigma-70, region 4 (pfam04545), but not always above their respective trusted cutoffs.	2.66588e-26
NZ_CP022203.1\|WP_095958515.1\|3426085_3427630_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	gnl\|CDD\|234854	PRK00881, purH, bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase; Provisional.	0
NZ_CP022203.1\|WP_095958525.1\|3452495_3452837_+\|(2Fe-2S)-ferredoxin-domain-containing-protein	gnl\|CDD\|239278	cd02980, TRX_Fd_family, Thioredoxin (TRX)-like [2Fe-2S] Ferredoxin (Fd) family; composed of [2Fe-2S] Fds with a TRX fold (TRX-like Fds) and proteins containing domains similar to TRX-like Fd including formate dehydrogenases, NAD-reducing hydrogenases and the subunit E of NADH:ubiquinone oxidoreductase (NuoE). TRX-like Fds are soluble low-potential electron carriers containing a single [2Fe-2S] cluster. The exact role of TRX-like Fd is still unclear. It has been suggested that it may be involved in nitrogen fixation. Its homologous domains in large redox enzymes (such as Nuo and hydrogenases) function as electron carriers.	6.47929e-21
NZ_CP022203.1\|WP_095958526.1\|3452992_3454792_+\|glycosyl-hydrolase	gnl\|CDD\|119365	cd06548, GH18_chitinase, The GH18 (glycosyl hydrolases, family 18) type II chitinases hydrolyze chitin, an abundant polymer of N-acetylglucosamine and have been identified in bacteria, fungi, insects, plants, viruses, and protozoan parasites. The structure of this domain is an eight-stranded alpha/beta barrel with a pronounced active-site cleft at the C-terminal end of the beta-barrel.	2.79645e-142
NZ_CP022203.1\|WP_095958520.1\|3433951_3435322_+\|O-antigen-ligase-family-protein	gnl\|CDD\|377422	pfam04932, Wzy_C, O-Antigen ligase. This group of bacterial proteins is involved in the synthesis of O-antigen, a lipopolysaccharide found in the outer membrane in gram-negative bacteria. This family includes O-antigen ligases such as E. coli RfaL.	1.73853e-10
NZ_CP022203.1\|WP_095958518.1\|3431725_3432838_+\|YjgP/YjgQ-family-permease	gnl\|CDD\|367632	pfam03739, YjgP_YjgQ, Predicted permease YjgP/YjgQ family. Members of this family are predicted integral membrane proteins of unknown function. They are about 350 amino acids long and contain about 6 transmembrane regions. They are predicted to be permeases although there is no verification of this.	6.37695e-79
NZ_CP022203.1\|WP_095958524.1\|3449109_3451890_-\|vitamin-B12-dependent-ribonucleotide-reductase	gnl\|CDD\|235828	PRK06556, PRK06556, vitamin B12-dependent ribonucleotide reductase; Validated.	0
NZ_CP022203.1\|WP_043713138.1\|3459038_3460346_+\|hypothetical-protein	gnl\|CDD\|275097	TIGR04275, beta_prop_Msarc, beta propeller repeat, Methanosarcina surface protein type. This model describes a repeat region found mostly in cell surface proteins of various methanogens. Methanosarcina barkeri, for example, has twenty such proteins, often with either seven or fourteen repeats. These repeats resemble the beta propeller repeats of the TolB periplasmic protein of Gram-negative bacteria, part of a complex associated with various functions including biopolymer transport (see TIGR02800).	0.000306216

>NZ_CP022203.1|WP_095958522.1|3439308_3441249_-|trypsin-like-peptidase-domain-containing-protein
MKRIPLACLVTALVTGAPALASDAVCQQEEAAASSSSQRLTKVGEDVFRRFETTHPYATTRIRASDGPIHTDVITHPGAAYIAPHFERLDVEEGDFVVVRSPDGTRKWRYDNSHPGARGGFWAIHIPGDTAIIELHSRDSVNRRGILNKHGYVIDRYARGYSNEEMGLSDNKALCGADDSQWAPCYASSDPAIYGRARPVARLLINGSGACTGWLVGSQGHLMTNQHCIGSASEAQNTNFEFMAEGASCSTSCASWFGCPGTVIPGGTLVKVDAPRDYALIQLSQNPANTYGYLQLRSTGAVVDERIYVPQHPAGHGKKIAVRSTHTQDQSGFAEVYSRNEASCQSGGPNDIGYYADTQGGSSGSPVIGHADNLVVALHHCAYCPNRGVPIESVISHLGTSLPECALPAAGCNPNGNGEPPPPPPPPPPPPEDSFDYTASNTASATQNTTNHVIALTAGQTLTVATCGLTGTQFTGDTWLRLRNPAGTEVASNDDACGGRGSSITFTATTAGNHEVRAGCYSSGSCTGRVVWETTGGSGGPTSGSFDFSASNTASAQQNTTNRDVTVAAGQRISVATCGVAGAVANGDTYLRLYNGTTQAASNDDGCSSGLGSSLSFTATTSGPLQIRAGCYSSNSCSGTVVWSID
>NZ_CP022203.1|WP_013939498.1|3437844_3439239_+|undecaprenyl-phosphate-glucose-phosphotransferase
MFSRLQRFYTSIKVVADMVMLAMAFVLAYATRFSGIVPVTEGIPPWTDSFFSLVMVLVIFPVTFHQSRLYGTNRSRTNTGEVFEVFKSTITAALILVAVTYFVRERYSRLTLAIFIVYAFTLVTCSRLVFRYVLSEVRRRGHNLKSILVIGAGDLGQRVIETVEHHRELGFRVMGVLTLRQEKVGQYVHGVRIIGHVDQVNEVLDAHPVDQVILALPLEGHAHVKGLMDKLALRTVDVRVVPDLYQYITLYGGLEEFGGLPIIRLQGDPMEGWSQVAKRAFDITFSLLAILITSPLMVATALAVRLTSRGPMLYRQERMGMDGRTFPILKFRTMRIDAEHSGAMMARPDDPRRTVIGTFLRKYSLDELPQFFNVLRGDMSLVGPRPERPVFIEEFKRQIPRYHLRHKVKAGITGWAQINGLRGQTCIEKRIEYDLYYIENWSLLMDLKILVRTALGGFLSKNAY
>NZ_CP022203.1|WP_157757502.1|3436481_3437591_+|glycosyltransferase
MKVALVHDWLVTHRGGERVLDALCEVLPGADIYTLIHKPGSQSPAIESRRIFTSFLQHLPGIHSRYRHFLPLMPKAIESLRLQGTYDLVLSSSHCVAKGLRTPRGTPHLSYVHAPMRYMWDLFDDYFGPGRTGLPVRAAAHAVRPWLRRWDRRTAAGVDRFVANSRHIAAKVRRFWGREASVVHPPVALERFAQVPLEGGGQGGYFLWLGAFAPYKRLDIALEAFRGLDAPLWVVGTGQDAARLGGESLPANIRFLGNVLDASLPALYRDARALIFTPEEDFGITPLESQATGRPVIAYAKGGALETVTNQTGIFFQEQTPAALAAAVRRFDAWEQGFRPEDARAQAERFSRARFQQAMLEEIDAILRG
>NZ_CP022203.1|WP_095958521.1|3435273_3436395_-|glycosyltransferase-family-4-protein
MWYAGAVAHVLLDLRMVRGRLHGIARYALELARRMPALAPDLRFSALVPPEGLAPGLGELTPRMPLHRARAGFLSPLEQPALAADLLQLAPEAFHATSFSLPLFWGGRLVATLHDANHLALADQYTPAQSLYYRVVVGPRARRASALVTVSEFSRDEIARHLKLSPYRLQVIHNGVDARFQPPTQAEAAAFRERHELPARYVAAVGNAKRFKNLALLKDFAGDLPVPVVLLAGKGAVAHELGLHENVLDLEELPEDEMPLFYGAAAALLLPSRYEGFGLPALEAMGAGCPVLASDTSSLPEVVGNAALKLPPDDAAAWREATLRVLRDDALRRELVELGRERVARFTWDDCARRTLAVYRRVLEASAPGGARG
>NZ_CP022203.1|WP_095958520.1|3433951_3435322_+|O-antigen-ligase-family-protein
MSTPMGTASELPLDPRWRRAVNAVLVTWTVGLVLAEVVLQVATGAAVLLAVLLRVGGRLRLPPDVRAYVGASVGLCLWQAVSPAVALLTGAAEAWPRGARYGQVLDSVAGAAAACVGAAGVPWLLLAGVLAGGWLVAALLGMFQNRVRWSVELPAFLKLNLGRLHENFGTEESPRYAAGGFFSHRLRFAHGAIAALGPALAVLGGAEHARRRVLAGAVVMGMLLSIYNAFARAALGAALLVSVVALLLLVQGSARKVGLALLVALVAVVSMSPAWRARMEKALGNLYGGEREHAMVVGWSLVREHPLTGVGFGNHKPAALATQDETGITDLLATDSHNLWLTVWAETGLVGLLLALAMHGFLGRALIRRYREGSLAATGALLSWVGFHILAMVHYLPFHSSVYLSFSLVWGLGLCEGSERLRGGTARPALDALTEAPGAAPYPRAPPGAEASNTRR
>NZ_CP022203.1|WP_095958519.1|3432834_3433950_+|YjgP/YjgQ-family-permease
MRATLFSYVLRAYVRYALGMLAGLVLVFVVVDFVDRAKLYTGPGWVRDAAELYFYKAMMSVQQLGPAALLLAAGTTVSALRKQGEVTAIRALTFGPSALYLPILVASFVACAGLVVFDERVATYSGRRVDEITTQRFNKWGDWRFYYTPKQWFRRGDNIFFLRGGSAQEGFQDVSVFTVTESFDLRRRLDASGMFPVEGMRWRLTDVVERTFDGEGKTSVRRLPEAEYALGVAVTAFRIRPGRPEQMRASELREQIDARRDVGLATKQFELALHNRFAYPMAAFPAALLGVGLALRANRRGHLTAAIIEGLLTAVAMWGLMMVCRTLVLTERLSPGVAAWTPTVLLALVAGAVWLQREGLLHLPRRSLLVR
>NZ_CP022203.1|WP_095958518.1|3431725_3432838_+|YjgP/YjgQ-family-permease
MNSLSRYLLRELLVPLGVWVAFMFLLLFVMQFLRGTDVLLGSSVTLVDLARLLAYLAPHFLMMALPIAFLLAILLGLGRLAEDRELTALQSLGVGPSRLVAAPLGIAVALSALMLVMTSTAQPWGLSGLKVLVSEVIRKNAVGDVKSGVFYEDLSDLTLYAEQVSADGKWTNVLLHDDREADAPLLVLARRGQVGTSTSGEVLRFALAAGEVHRSAGGEAEEYSVIRFDEAEISVGLGASMGKRSRFSFSREELTPAELMAAARDAEARGEDPRVFRMALHSRLGSALAPIAFALLGTPLAMGRRQSGRAWGYLLTLGGYVLYYLLSRVFEQMGQKGQMPVALAGQMANLVFIAVGLVALYRVSRSGTLK
>NZ_CP022203.1|WP_095958517.1|3430463_3431729_+|phosphoribosylamine--glycine-ligase
MDVKVLLLGSGGREHALAWKLSRSPRLTRLLCAPGNPGTAKLGTNVALRADAPEEVAAFAKRESVDLVVVGPEAPLVAGVADALADVGIACFGPVAAGARIEGSKAFAKDIMAEAGVPTAAFRTFTDVAAAEAYAVAQGRIVVKADGLAAGKGVIVAHDVEAARAAVRAVGAMGVAGQTMVLEELLEGEEVSAMALCDGERYAMLPLSQDHKRVGEGDTGPNTGGMGAYSPAPFLSAEQLAEVGERVVAPTLAVLRRRGIPFRGVLYAGLMLTRSGPKVLEFNARFGDPETQVLMMQLGEDLLPLLDACARGTLTPRTLVSAPGASVGVVLAARGYPDAPEKGRRIEGLDAVPPDATVFLAGVEARDGGLVTAGGRVLTVCARGEDLARARERAYAAAAAVRFEGMHFRRDIGARGMKGAP
>NZ_CP022203.1|WP_095958516.1|3427633_3430462_+|zinc-ribbon-domain-containing-protein
MRIVCQKCAAAYAIDDKLITAKGVRAQCPRCRHLQLVRRDPSAAPAPAPQPPVTLTPVSGAGAAPAPNPADDLFGDFGAPPPAAAPAPTPARSEGAAGSDLFGDFGAMPASAPASSPPVDPFADLGAPAAARGPAAAEDPLLDFLGPPPSAPQGLEARAERPAKPAAPKPPATAGCRACQKPLTDSFDQALGICDDCRQPGAAQVPPAAASRPSAPAASADSLPPMADLGAGPSSGGGAQDPQPEPRGGARVPISTDIIPDMGPEPRSGARGSAPQLGAEPRSGPRAAPVRTSAAQHGGRARGGRGGLVAGLVGLVVVGGGVGGYFLYQQQQTARRDEGPPPAPAIPDAVQAVLPRWKLKYLEISGTSAERLAQGQQQLARDERFGYAEAEESFQQALLLDPTSDAAIAGYVQALALGRGARMDDATFQEARALLLAAESRSGRTAPLLLAHANLLLARSGQPEQARPLAEELLARAELPDAQKAEAHLVLGRTWLSSSRELARSHFDSAQKLAPDIKRLHYYRALAHASGGEYSAALDTLRERLEANPKDWESLALTARLYQEVGEPGEARKLYEARVKAEPGELRALLPLAMLRYQSEGSAAGAVRELRALLRNRARYDAPEVAEVLVHLAAAERTAGSQDAAAKSAEEALRLVKDLPEAHLQLFLVALGRRDAEKARAHLPGFRGQLEDGALEKVLEGRLLLLEKQPLVALEAFQAAVKLDARRLDAQLLAGVAAASAKRRDDAFRALHQALQSDPLRLEPRPVMSAYWVRPRETVDGVEGVILALAEGPEDPSPLLYEGLLRFHQHQLDAAERHFRGVLEVDANNAGALAYRSLIALQRGAVADARRLGERSAAAGRQMPVSHLALGLARAESRQVEPAKRALRDALALAPTLLSAQARLANLESPQGKAAAKDTLVKVVGLDPAYLPAKRMLYLLER
>NZ_CP022203.1|WP_095958515.1|3426085_3427630_+|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase
MLALLSVSDKRGLVPFAQGLVRLGFRLLSTGGTLEALKGAGVPVTKVSEHTQSPEILGGRVKTLHPRIHGGILGRLELDADREEMKAHGIEPISLVAVNLYPFRQTVASGAAEPDVIEQIDIGGPAMVRASAKNFRHVSVVVDPDDYPAVLAELEERKTVGEDTRRRLMRKAFAHTAAYDASISAWLSAQAGEAFPGELSLAFQKSQELRYGENPHQRGAFYREHATPQEPTVAFARVLQGKELSYNNILDLDAALGLLLEFPEAPAAVIIKHNTPCGVAVDDALVKAYRTARAVDEVSAFGGIVALNREVDAATAQAMAETFLEAVIAPSYSPEALQVLAAKKNLRLLEAGPALASPQARPRAQLDARSVSGGLLLMDRDSVEPPLSWKVVSKRAPTPEEERAMRFAWKVCKHVKSNAIVFASGARLLAQGGGQTNRVDSVRIAMQRGGEALKGSAVASDAFFPFRDGLDEAARAGATCVVQPGGSVRDAELIAAADEHGMAMVLTGVRHFRH
>NZ_CP022203.1|WP_095958524.1|3449109_3451890_-|vitamin-B12-dependent-ribonucleotide-reductase
MDKELSSKSTANGKERRNGRKARVAAKGLTVERFFTTPGVDPADELAWEYRSASITGEDGKAVFEQKNIEVPKSWSMLATNVVASKYFRGTPGTPERETSVRKLVARVVDTLTRWGVEGGYFTRDTDREAFHAELTHLLLRQKASFNSPVWFNVGVETQPQCSACFINSVEDSMDSILTLARTEGMLFKYGSGTGSNLSSIRGSKELLAGGGTASGPVSFMRGFDAFAGVIKSGGKTRRAAKMVILNAEHPDILEFIRCKSAEEKKAWALIEAGYDPSFNGEAYSSVFFQNSNNSVRVTDAFMKAVVDDAAWTTRAVRDGQPVDTYQARALFREIAEAAHLCGDPGMQFDTTVNGWHTCSGTARINASNPCSEYMFLDDSACNLASLNLMHFRTIDGDFDVTAFRHAVDILLMAQEIIVGNSRYPTERIEKNSHDYRPLGLGYANLGALLMASGLPYDSAAGRNYAAAITSLMCGEAYAMSARLAEKQGPFAGYANNAEPMLGVIRKHRKAAYHVAPEGVSQGLFAAQKDAWDRALALGEAHGFRNSQVTVLAPTGTIGFMMDCDTTGIEPDIALIKYKKLVGGGMLKIVNQTVPLALEKLGYPQTQAQDIISYLDKQDTIEGAPFLKPEHLPVFDCAFKPAQGQRSIHWMGHIQMMEACQPFLSGAISKTVNMPSDATVEDIEKAYMEAWKRGLKAIAVYRDGCKRTQPLNTSKDTRAAKATVAPEPAPAVQPEPRAVRRRLPDERRSITHKFSIGGHEGYLTVGMYEDGLPGELFIVMAKEGSVVSGLMDSFATSVSMALQYGVPLKVLVDKLSHTRFEPSGFTGNPDIPIAKSITDYIFRWLELKFLPSEEVDAVLDRVDVKPEREALPAQTASAQLPAANGSKRSTWLNQADAPPCHTCGAIMVRSGACYKCSNCGATSGCS
>NZ_CP022203.1|WP_095958525.1|3452495_3452837_+|(2Fe-2S)-ferredoxin-domain-containing-protein
MAPPFQRHVFVCTNRRPDGHPKGCCATKGAEEVRAAFKAELDKRGIKGSMRANAAGCLDTCSFGVAVVVYPEGTWYGGVKVEDVKDIVEQHLVEGRPVERLLMPFSRKVLAQD
>NZ_CP022203.1|WP_095958526.1|3452992_3454792_+|glycosyl-hydrolase
MRRSWWASGLIATALSVVGCDSEGPSFPTGDLTAFQEAALASEWAVGVTYAVGTRVTYQGRLYECRQPHTSQADWTPAAVPALWLDLGPSSGGEPDGGSGGTDAGTGGDVTAPTVGLNASSSRITAAGSLSVMATATDDVGVTRVELLENGAVVATGTQFSRAFTGWEQNGTYVYGVRAYDAAGNVGTTTLTVVVEIPGGPPPTGKRIVGYFTAWGIYARNYQVSNVQPAKLTHINYAFSNISPDGRCILGDPYADIDKGGGWQGEWDPGALRGNFRAFKELKRQHPHLKLLISVGGWSWSTHFSTVASSPASRAAFVKSCVDLYIRGQYPGVTPANGEGVFDGIDIDWEYPVGGGLPGNSNSPADKQNYTLLMQEFRSQLNAVTAQTGKPYLLTIATGASPDLLENKQETKKLSDVLDWINVMSYDYHGAFEPTTNFHSALNRVTGDPGASAGFYTEGSVSKMLQLGVPPAKIVVGVPFYGRGWGQVPNVNNGLFQPGIPIMGTWDDGTSGPTGVFDFKDIKNRFERAGSGYTKFFHPEAKQAYVFNPSTGVWIGYDDVQSITAKSDYILNNNLGGAMFWELSGDDGSLLDELARKLR
>NZ_CP022203.1|WP_095958527.1|3454885_3456085_+|hypothetical-protein
MSFAAAVLLVALSSSSVAAEPWTAVVRVASDEDRALLVRLRGQSSDLAVRLNVSPGAPFDGHPGGAWLAAERLAERHQARAVLWFAREGGDVRVQVAEFDSRRLFTRAARLGQSVGSLEWSTGAEALALAARSALRAVEVGAPLGDVVAVAPPRPPSADARLKPGGVMGASHPLDDVASGDGGATTRSAHAGGAAPVAEVVMAPVREGMAAAREGSGAPDGLEHPGRGVWLSVGGHAALDGYTRTGHQGVAVGVGFQPGRLRLRAQVLASVPRRLRDARTELTLGQHAASVWAGRPWAVTERWDVEAGLGAGAVLFTRRTQALAAEVEAAPPGSMLALLVGPELRARWMGARVGLEASLAGEVLLGRPELHYAIDGNFVSRGAGWAVRPRLGLAMVVFL
>NZ_CP022203.1|WP_157757503.1|3456081_3456723_+|sigma-70-family-RNA-polymerase-sigma-factor
MSADDPIGPAPPSMAAMRSSGSHAADPRRAAEDPRIQAAIQGEREATGALLMELLPRVRNLVRYLVRGDGDVEDIAQEALIALVRGLPSYRAEGRFQSWADRVVARTTFAWLKRSRGRDARHADAPVELVAVPSEDALPDEYVHRRHMVTLLDRLSNEQRHALVLHHVLELSVPEISTELGIPFETVRSRLRLGRTALRALATVEDDGGEGLG
>NZ_CP022203.1|WP_095958529.1|3456719_3457628_+|tetratricopeptide-repeat-protein
MSDFREEGDGALNALVLPLDEAAGPARRISRERSAQMVLAALEAGALVAQPAPRPRAKRPPVWLMTGALLVAGAAAAAVWSFTRPGAVPTPQVEDASLTAAPRPRPGDPGARGSEPSPRGALSARDAEGDSGAHGASAAARVTEGPPGAEALPAASSAGAPGPARSLAPAASAKPGAQEDLLLKANGLRSEGRWKEAESLYLRVIRAEPSSLASYVARVASGSLRLEHLGDAPGALRQFKAALRLQPRGVLDQEAQHGIAEAHRVLGDRDAERGALEAFLAAHPDSPLVPSARARVRELTAP
>NZ_CP022203.1|WP_043713138.1|3459038_3460346_+|hypothetical-protein
MFAKGRLHMKREVKAGITGLVFGSMLVGCGVAPEQDGQGGVEDATTEAQAQASTERVLEESGGYVEPDPLARYWPAVAYGGGKFLAVWTDVRTGGIYGTRVKPDGTVLDGEGIRVNIGDEEGVRPGIGFNGKYFFVVWESRDGVDGVRVKPDGTVVGPVFRAIQTGESFGPVRVACSPKICLVTYTISGDFSTIYFTRVTKDGVVLRTADRTLSASNTFAYDASPTWNNKTKEFLVVWSDEHGEGPENADIYGNRVKEDGTILDGNGFPISDAEGTQSTPDVEWTGKSYQVVWTDDRNGNPDIYGARVSKTGTVKDPEGIPISTAAGAQADPRIAHHNDKSLVVWDDQRDGPHSIWGARWGEDGDVWDPAGFPISTGDQPQEYVPDVAYGSNKFFTVYAGQETFEPFEPHFILGTRVTHQAELKDVPAIPLTREP
>NZ_CP022203.1|WP_157757504.1|3460471_3460990_-|transposase
MDETGHTFRARLGTTWAPVGQVRVLKRLSRRREISSVVLLTAPRGRERPKVFARHFVGAVHDKEVIAALRYFHRRLGRPLVIIWDRLQAHRSKAVRAWLQRHSKDVLVEWLPPYAPDLNPEEGCNGVVKEALLNATPPAISDLMRLARREFRALQHRPDVLRSFFEHAGLDV
>NZ_CP022203.1|WP_095958531.1|3460905_3461514_-|winged-helix-turn-helix-domain-containing-protein
MKGVVVMGQQPFRLTPEQMEERRLFAASLLKSGWRPVDVADECGVTRGAVSQWCKALAQGGVRKLRRKPHQGRPSQLSPSQWKQVARALNAGAVRAGFPTERWTLPRIAHLIEHRWGVRYHPRSLTRPLHRLGFSAHRPRSQASERDDALIEAWVRRDWPRIKRGLEEAGGQLPSWMRRVTRFGPAWAPPGRRWDKSESSSV
>NZ_CP022203.1|WP_095958532.1|3461556_3463029_-|hypothetical-protein
MQEFIDVLRSQARHIAPDLARLAYQRGLAVTRPDGTTRPIPITATPVVLDAAEIRRRAELSARLSSATVKMAQAQLQGPDAEALLGALSPLERVLAERTWRQSTRLATTRVDYFVAGGTPWALEVNATIPAMQGYSDIAARTFIEVVGRYFRYPEKALHALLSLNGSNALALYRSLLDGYAAERNGRMPDTVALLCRRNDAQITELRWLCERFREFGADADLVHPDEVSGDDAFVAHGKKYDLVYRHLFVRRLEESPSLWVEDFLGTVPGKKAVFLNPPASQVEVKLTFARLSQALAEPALAEAAQLTGEELEAVRASVPWTRVFQPGPTRGPDGEQVEDMVALVAATPARFVLKRSWDYGGRAVFLGRSAGTVPYTERVQAAYGAPMTWAELCARTAADRAGGGFVVQEVVDSPPEDHLLCEPNGTVLPASFFVDYSAYASVGLARQPAWGGVCRGSLSEIVNIVGGGGVLPLITTEVASKLLMAWKAF

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Crispr_ID: NZ_CP022203_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_6

3528776-3528888

Orphan

Consensus_repeat	Method
TCGGAGCACCGCTCCCTGGAGTC	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP022203_6

>merge|NZ_CP022203|6|3528776-3528888|CRISPRCasFinder
TCGGACCTGCGCTACCTGGAGACCTCGGACCGTGCGCCAGGCGCGTCCGAGCGCCGCTATCTGGAAGCACCTCCCCGAGCGCAGGGAGCATCGGAGCACCGCTCCCTGGAGTC

>NZ_CP022203|6|5|3528776-3528888|CRISPRCasFinder
TCGGACCTGCGCTACCTGGAGAC	CTCGGACCGTGCGCCAGGCGCG
TCCGAGCGCCGCTATCTGGAAGC	ACCTCCCCGAGCGCAGGGAGCA
TCGGAGCACCGCTCCCTGGAGTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095958560.1\|3510350_3511496_-\|cysteine-desulfurase	unknown	unknown	gnl\|CDD\|224029
NZ_CP022203.1\|WP_095958565.1\|3519172_3523675_-\|response-regulator	unknown	unknown	gnl\|CDD\|274008
NZ_CP022203.1\|WP_013939576.1\|3541774_3542512_+\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|376576
NZ_CP022203.1\|WP_095958567.1\|3529397_3530987_+\|DUF1957-domain-containing-protein	unknown	unknown	gnl\|CDD\|212104
NZ_CP022203.1\|WP_095958563.1\|3516254_3517670_-\|patatin-like-phospholipase-family-protein	unknown	unknown	gnl\|CDD\|366777
NZ_CP022203.1\|WP_095958568.1\|3531084_3532560_+\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|273938
NZ_CP022203.1\|WP_095958564.1\|3517687_3518626_-\|MoxR-family-ATPase	unknown	unknown	gnl\|CDD\|223786
NZ_CP022203.1\|WP_013939572.1\|3535702_3536548_+\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|188247
NZ_CP022203.1\|WP_013939559.1\|3513726_3515067_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|223679
NZ_CP022203.1\|WP_095958571.1\|3542531_3543053_+\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|223917
NZ_CP022203.1\|WP_043712923.1\|3512767_3513610_-\|Fic-family-protein	unknown	unknown	gnl\|CDD\|376885
NZ_CP022203.1\|WP_095958570.1\|3537918_3539040_+\|DNA-protecting-protein-DprA	unknown	unknown	gnl\|CDD\|376794
NZ_CP022203.1\|WP_013939575.1\|3539051_3541613_+\|type-I-DNA-topoisomerase	unknown	unknown	gnl\|CDD\|235840
NZ_CP022203.1\|WP_095958561.1\|3511492_3512614_-\|DHH-family-phosphoesterase	unknown	unknown	gnl\|CDD\|223691
NZ_CP022203.1\|WP_013939570.1\|3532744_3534679_-\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP022203.1\|WP_095958569.1\|3536544_3537780_+\|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|212030
NZ_CP022203.1\|WP_095958572.1\|3543055_3543637_+\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP022203.1\|WP_095958562.1\|3515206_3516154_-\|branched-chain-amino-acid-transaminase	unknown	unknown	gnl\|CDD\|235841
NZ_CP022203.1\|WP_013939563.1\|3518815_3519037_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961585.1\|3523774_3526843_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|340831

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095958560.1\|3510350_3511496_-\|cysteine-desulfurase	gnl\|CDD\|224029	COG1104, NifS, Cysteine sulfinate desulfinase/cysteine desulfurase and related enzymes [Amino acid transport and metabolism].	2.31724e-162
NZ_CP022203.1\|WP_095958565.1\|3519172_3523675_-\|response-regulator	gnl\|CDD\|274008	TIGR02168, Chromosome_partition_protein_Smc, chromosome segregation protein SMC, common bacterial type. SMC (structural maintenance of chromosomes) proteins bind DNA and act in organizing and segregating chromosomes for partition. SMC proteins are found in bacteria, archaea, and eukaryotes. This family represents the SMC protein of most bacteria. The smc gene is often associated with scpB (TIGR00281) and scpA genes, where scp stands for segregation and condensation protein. SMC was shown (in Caulobacter crescentus) to be induced early in S phase but present and bound to DNA throughout the cell cycle. [Cellular processes, Cell division, DNA metabolism, Chromosome-associated proteins].	5.09872e-27
NZ_CP022203.1\|WP_013939576.1\|3541774_3542512_+\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|376576	pfam01618, MotA_ExbB, MotA/TolQ/ExbB proton channel family. This family groups together integral membrane proteins that appear to be involved translocation of proteins across a membrane. These proteins are probably proton channels. MotA is an essential component of the flageller motor that uses a proton gradient to generate rotational motion in the flageller. ExbB is part of the TonB-dependent transduction complex. The TonB complex uses the proton gradient across the inner bacterial membrane to transport large molecules across the outer bacterial membrane.	1.08275e-18
NZ_CP022203.1\|WP_095958567.1\|3529397_3530987_+\|DUF1957-domain-containing-protein	gnl\|CDD\|212104	cd10792, GH57N_AmyC_like, N-terminal catalytic domain of alpha-amylase ( AmyC ) and similar proteins. Alpha-amylases (alpha-1,4-glucan-4-glucanohydrolases, EC 3.2.1.1) play essential roles in alpha-glucan metabolism by catalyzing the hydrolysis of polysaccharides such as amylose starch, and beta-limit dextrin. This subfamily is represented by a novel alpha-amylase (AmyC) encoded by hyperthermophilic organism Thermotoga maritime ORF tm1438, and its prokaryotic homologs. AmyC functions as a homotetramer and shows thermostable amylolytic activity. It is strongly inhibited by acarbose. AmyC is composed of a N-terminal catalytic domain, containing a distorted TIM-barrel structure with a characteristic (beta/alpha)7 fold motif, and two additional less conserved domains. There are other two canonical alpha-amylases encoded from T. maritime that lack the sequence similarity to AmyC, and belong to a different superfamily.	0
NZ_CP022203.1\|WP_095958562.1\|3515206_3516154_-\|branched-chain-amino-acid-transaminase	gnl\|CDD\|235841	PRK06606, PRK06606, branched-chain amino acid transaminase.	9.45331e-172
NZ_CP022203.1\|WP_095958568.1\|3531084_3532560_+\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|273938	TIGR02037, Probable_periplasmic_serine_protease_do/HhoA-like, periplasmic serine protease, Do/DeqQ family. This family consists of a set proteins various designated DegP, heat shock protein HtrA, and protease DO. The ortholog in Pseudomonas aeruginosa is designated MucD and is found in an operon that controls mucoid phenotype. This family also includes the DegQ (HhoA) paralog in E. coli which can rescue a DegP mutant, but not the smaller DegS paralog, which cannot. Members of this family are located in the periplasm and have separable functions as both protease and chaperone. Members have a trypsin domain and two copies of a PDZ domain. This protein protects bacteria from thermal and other stresses and may be important for the survival of bacterial pathogens.// The chaperone function is dominant at low temperatures, whereas the proteolytic activity is turned on at elevated temperatures. [Protein fate, Protein folding and stabilization, Protein fate, Degradation of proteins, peptides, and glycopeptides].	3.11863e-147
NZ_CP022203.1\|WP_095958564.1\|3517687_3518626_-\|MoxR-family-ATPase	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	2.47955e-41
NZ_CP022203.1\|WP_095958569.1\|3536544_3537780_+\|LysM-peptidoglycan-binding-domain-containing-protein	gnl\|CDD\|212030	cd00118, LysM, Lysin Motif is a small domain involved in binding peptidoglycan. LysM, a small globular domain with approximately 40 amino acids, is a widespread protein module involved in binding peptidoglycan in bacteria and chitin in eukaryotes. The domain was originally identified in enzymes that degrade bacterial cell walls, but proteins involved in many other biological functions also contain this domain. It has been reported that the LysM domain functions as a signal for specific plant-bacteria recognition in bacterial pathogenesis. Many of these enzymes are modular and are composed of catalytic units linked to one or several repeats of LysM domains. LysM domains are found in bacteria and eukaryotes.	4.85053e-06
NZ_CP022203.1\|WP_095958572.1\|3543055_3543637_+\|biopolymer-transporter-ExbD	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	5.26741e-14
NZ_CP022203.1\|WP_013939559.1\|3513726_3515067_-\|AAA-family-ATPase	gnl\|CDD\|223679	COG0606, COG0606, Predicted ATPase with chaperone activity [Posttranslational modification, protein turnover, chaperones].	3.4446e-09
NZ_CP022203.1\|WP_095958571.1\|3542531_3543053_+\|biopolymer-transporter-ExbD	gnl\|CDD\|223917	COG0848, ExbD, Biopolymer transport protein [Intracellular trafficking and secretion].	1.09726e-08
NZ_CP022203.1\|WP_043712923.1\|3512767_3513610_-\|Fic-family-protein	gnl\|CDD\|376885	pfam02661, Fic, Fic/DOC family. This family consists of the Fic (filamentation induced by cAMP) protein and doc (death on curing). The Fic protein is involved in cell division and is suggested to be involved in the synthesis of PAB or folate, indicating that the Fic protein and cAMP are involved in a regulatory mechanism of cell division via folate metabolism. This family contains a central conserved motif HPFXXGNG in most members. The exact molecular function of these proteins is uncertain. P1 lysogens of Escherichia coli carry the prophage as a stable low copy number plasmid. The frequency with which viable cells cured of prophage are produced is about 10(-5) per cell per generation. A significant part of this remarkable stability can be attributed to a plasmid-encoded mechanism that causes death of cells that have lost P1. In other words, the lysogenic cells appear to be addicted to the presence of the prophage. The plasmid withdrawal response depends on a gene named doc (death on curing) that is represented by this family. Doc induces a reversible growth arrest of E. coli cells by targetting the protein synthesis machinery. Doc hosts the C-terminal domain of its antitoxin partner Phd (prevents host death) through fold complementation, a domain that is intrinsically disordered in solution but that folds into an alpha-helix on binding to Doc.This domain forms complexes with Phd antitoxins containing pfam02604.	1.81664e-10
NZ_CP022203.1\|WP_095958570.1\|3537918_3539040_+\|DNA-protecting-protein-DprA	gnl\|CDD\|376794	pfam02481, DNA_processg_A, DNA recombination-mediator protein A. The SMF family, of DNA processing chain A, dprA, are a group of bacterial proteins. In H. pylori, dprA is required for natural chromosomal and plasmid transformation. It has now been shown that DprA is found to bind cooperatively to single-stranded DNA (ssDNA) and to interact with RecA. In the process, DprA-RecA-ssDNA filaments are produced and these filaments catalyze the homology-dependent formation of joint molecules. While the E.coli SSB protein limits access of RecA to ssDNA, DprA alleviates this barrier. It is proposed that DprA is a new member of the recombination-mediator protein family, dedicated to natural bacterial transformation.	7.28426e-79
NZ_CP022203.1\|WP_013939575.1\|3539051_3541613_+\|type-I-DNA-topoisomerase	gnl\|CDD\|235840	PRK06599, PRK06599, DNA topoisomerase I; Validated.	0
NZ_CP022203.1\|WP_095958561.1\|3511492_3512614_-\|DHH-family-phosphoesterase	gnl\|CDD\|223691	COG0618, COG0618, Exopolyphosphatase-related proteins [General function prediction only].	8.86674e-50
NZ_CP022203.1\|WP_013939570.1\|3532744_3534679_-\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	2.99294e-62
NZ_CP022203.1\|WP_095958563.1\|3516254_3517670_-\|patatin-like-phospholipase-family-protein	gnl\|CDD\|366777	pfam01734, Patatin, Patatin-like phospholipase. This family consists of various patatin glycoproteins from plants. The patatin protein accounts for up to 40% of the total soluble protein in potato tubers. Patatin is a storage protein but it also has the enzymatic activity of lipid acyl hydrolase, catalyzing the cleavage of fatty acids from membrane lipids. Members of this family have been found also in vertebrates.	1.13156e-13
NZ_CP022203.1\|WP_013939572.1\|3535702_3536548_+\|tetratricopeptide-repeat-protein	gnl\|CDD\|188247	TIGR02795, Uncharacterized_protein_in_oprL_3'region, tol-pal system protein YbgF. Members of this protein family are the product of one of seven genes regularly clustered in operons to encode the proteins of the tol-pal system, which is critical for maintaining the integrity of the bacterial outer membrane. The gene for this periplasmic protein has been designated orf2 and ybgF. All members of the seed alignment were from unique tol-pal gene regions from completed bacterial genomes. The architecture of this protein is a signal sequence, a low-complexity region usually rich in Asn and Gln, a well-conserved region with tandem repeats that resemble the tetratricopeptide (TPR) repeat, involved in protein-protein interaction.	6.72129e-19
NZ_CP022203.1\|WP_095961585.1\|3523774_3526843_-\|glycosyltransferase	gnl\|CDD\|340831	cd03801, GT4_PimA-like, phosphatidyl-myo-inositol mannosyltransferase. This family is most closely related to the GT4 family of glycosyltransferases and named after PimA in Propionibacterium freudenreichii, which is involved in the biosynthesis of phosphatidyl-myo-inositol mannosides (PIM) which are early precursors in the biosynthesis of lipomannans (LM) and lipoarabinomannans (LAM), and catalyzes the addition of a mannosyl residue from GDP-D-mannose (GDP-Man) to the position 2 of the carrier lipid phosphatidyl-myo-inositol (PI) to generate a phosphatidyl-myo-inositol bearing an alpha-1,2-linked mannose residue (PIM1). Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct 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. The members of this family are found mainly in certain bacteria and archaea.	4.17189e-46

>NZ_CP022203.1|WP_095961585.1|3523774_3526843_-|glycosyltransferase
MPGPSGSSRRLTEYLKALPDRFSVVVLSAKTPDHSHIEKYQGARLLRVPVGSGDLASRIQAFERAVRRQLESEDYALAHFTDPFGGYALCELKGDYGYRLIYEAQTFPSQELRYTHPQTEGDRRFLSKIRRQELFCLMNADLVVTGSEATRAYIQSLGASEDQVRVLPAPVDLAPFSPDVLGAPDGEPLRMMYLGSQVGWQGLSTLLRAVALAARHEEVRLTVVGARHADWQPHLDDLVKELKLGDRVEFQPPVNHDDLAKVLALADVGVLPLEDVERNRVQGGPLAKASEYCAAGRPLIAADLPVTRELIPEAAGLFFPPGDSQALADRILELARDVPRRLELGRAARAHAEEALDAGLIRGKLLDLYDSLLEKRSEPVSTTSEDDLPAPTTVTGTPTNRLAALLPPEPAPTAAPVARSKAPEPRKDKDAPATKPSKKEDLPLVLGQVLDEGLDTRLVKTELESNPIGPPVVMGAPLREQPSTAGAEAATPRPSEDPENSLPIVQATEFEDADEPPSARAASTADDASGPSEPTPVTKAPPPSGRHPAFASADGEEDAGTTPVTKAPSPSGRPPVSSGPDTPESAGTTPIVKVPPPPVRLPSTSSTDGAEASAATPVVKVPPPPGRPPPPVSADAGETPAPTPIVKAPAALNRGEARASEGTGESDEAPAPTPVVRSPVLGARYEPPSHTPVVRSPFERERDEPPAPTPIIRVPTELLRELLPSRSPSGGRGAQGSGRPDEHPTPTPIVPAPSPLSSRSISARMETPAGRMPSLTERSKTSEHERTPPVLRSGPGAPDGERLPPIRGGTAASTPERPAPTLHPSAATPEADRPPALPPRAATPPPVPRQRPPTLQSVDGPPRLEPLSPRTLKASAPLPSAEDEEPEEISEDEAESLDEGDDSPPRDRPQPDEPDEISSDEVEEAEISASSAAQLIDTDDDLEEADADVAPASPDEGPAPEPVPSTLNPWFAQLAHGYCPPDGIRFDRHTPPTTFPGRDEPTNPAHPAPSGRPEVVVRGKSS
>NZ_CP022203.1|WP_095958565.1|3519172_3523675_-|response-regulator
MERRVLIVESDHELALSMATVLKGAGYQTNLAETSADAQRELEKRRPDLVVLRAELKDQSGFVLCGNIKKGKWGQNLKVLLISSESGVEGLAQHRQTPQAADGYLAFPFELGDLTALSHGIVPPGTDDTSASLDAALNGTREAPPPMPPSLKAAGGPPKLPKRERRSAMTEEDRAFLDRTFQSIAERKAELLAESRQLKRPPPRRELMGTPEGKIQILRDELKTREAQLARLSEIWSVRERELLSGEDRIHEKDVELQGLKMQVDDLLRRFNEAQQATIQKEREHGATVDDLLLQKFSAEKDLIEVVASKEKDINLLRREVSRAEEELARRASELEHGRNEYDKLEKHLGVVTLEFEVKEQKLQDTVLANEGEIARLTRRGDDFEAELGRTISERDQRFAELDGEIQALQERLQQTEQERDTTVRGLEARAARAEEHGTQADAEIHRLNAERDALEAKLSQQVADLETDLARTTGERDQLRLDKDAQEAELTRRVEERDAKLGTLERELSETIARNEHTEAELNANIQQHLERIGELEGEVEAVKAHLDDRENELTAELQALGQAKDELETDLNDRLQALSQAKAELEADLTGQIQALTSQLEETQRQLDDSQRTGEQRSARVAMLEDTVAQRDGTIEALQGDVAARDQRISELSGDLEATSQTLTQTQQTLAQTEQQLADTQNTLASTEGTLAQTRGELDATSQTLADTQARLSDTEGTLAQTRGELEATSQTLTQTQQTLAQTEDSLAQTRGELDATSQTLTQTQQTLAQTEQQLADTQNTLASTEGTLAQTRGELDATSQTLAQTQQQLASTEGALAETRGELDATSQTLAQTQQTLAQTEDSLAQTRGELDATSQTLGQTQQTLAQTEQQLADTQSTLASTEGTLAETRGELDATSQTLADTQARLSDTEGALAQTRDTLAHTTHERDQRIAELADLGAAKDALEQDLTGQIGQLRSELSETQGNYEAERAAHEKLAAESSAHIGDLTSERDGLRAELEATSQTLEQTQGQLAATRDALAKEQHAHQESRKAAANTQAALEGQLAEARAHGEDLGEHLTLTKHELGTRVAEVTQLTATLAQAENARATLEERLHTLTEESQRREELLQHDLTQKGTELSDTLRKLTHVTQEKMRQAEVLNREVATRTEQLKAMEARLQAQATEARRQAEGLGQQVAGLNEQLEQGRKALAGREDQLRAAGTAQQKLTAERDGLAGQLQQAEARLQQQAQQATQERADAKRAADELAAKLAKAEQRVAQLTQDAQTQAAEHDARAKELQGQLTARAKKIQDLELAVENAHGTKARAEKELNAKVAAAEARAHEATTRLAAAQKERKDLEARHAKEQEELTAKQKAELERRDTIKAQEVARLQQSVQEKSKALKVAELELARYKSKSTAAASKAAARPAEDDDLAVRTQLNQVIPPTAAPAAPAKKAAARPAAQAAAKKAPAPAPAPAPAPPAALSDDSEPTDRTLLIQLPTAKEDDDWTALVDELDK
>NZ_CP022203.1|WP_013939563.1|3518815_3519037_+|hypothetical-protein
MVWAWIRMVMMVAVVLLPGGFPLLLAYVSLRTLRNSWRRAQEEALSDGHQVTLREVVSTLHFKELVREARASL
>NZ_CP022203.1|WP_095958564.1|3517687_3518626_-|MoxR-family-ATPase
MSTPSTVESRAFTSVEDAEKRLEQVGYLSSPEIATAAFLADRMDKPILVEGPAGVGKTELAKALSQALGREFIRLQCYEGLDEAKALYEWEYAKQLLYTQLLKDKIGDMVQGTTTLAQAADRLASSDAVFFSERFLLPRPVLRAQLSERPALLLVDEIDKADPEFEAFLLEVLSDNAVTIPELGTFRARHIPRVLLTSNAARELSDALKRRCLHLHIDFPDRERELRIVRARLPQVPQVLAEQVVEAVAAIRALDLKKAPSISETLDWAQSLALLNAEQLTSDVVASTLNLVLKYEGDIEKAKANLPQIAQA
>NZ_CP022203.1|WP_095958563.1|3516254_3517670_-|patatin-like-phospholipase-family-protein
MLLKERFQITRPLEEMELRLVRASLANAALVDPREEAILRTALSLARLYKVRHGGLDVGVGAQLTPFREEVERRLGPVLRGPTPPTRDRLMPHVKDLRQHAAKARDAVAERLRGRVPLEALDREIRHKELVLVTGGGGGTAYVYLGVMSLLDEHGLEPRLLAGTSMGAILAIMRSRLARFDPTDMINIVRGLSFRKLFRFISTESRYGLPAALRLFLRAGLGRFFGAGPESSGMRLRDLPVPTLIAVGGIRRGMLPRPLEYYERLLGTSPLGLLNPAGVARRIQAAMGAMAELFTRPEVTARLYLGADDATGDFDALDAAGFSSALPGVIHYDVLREDPAMHTLVEGLMGQHGVARLIDGGLVDNLPAKAAWKAVARGRIGTRNAFILALDGFAPKLTTPFWLPLQRLAAMTVAPNLPYTHHVKRFPRTLSPVEVVPSVELAAKALHFGRAALAEDIPFLRRMLAPLPPVL
>NZ_CP022203.1|WP_095958562.1|3515206_3516154_-|branched-chain-amino-acid-transaminase
MSSTSSSGVRAEQIWLDGRLMKWDEGHVHLMTHALHYGLGVFEGIRAYKTHDGRLAVFRLREHIRRLLDSAHIIMLKIPYTEDELFDACVNLLRAQKDLFANGAYLRPVAFMGDGAMGLGAVNPTRTAVTAWDWGAYLGDKGIKEGIRAKVSSYTRMHVNVNMVRGKITGQYVNSILAKREAVMAGYDEAILLDVSGFVAEASGENIFQVNKKGVIKTPPLSCPILDGITRDTVLHILRDSGRTVEEVTFTRDALYITNEIFFCGTAAEITPVREVDNRQVGDGKPGPITRHVQDMYFRIVRGQEPKYAEWLTYI
>NZ_CP022203.1|WP_013939559.1|3513726_3515067_-|AAA-family-ATPase
MAPPAGYDYDDNPFKLENPSILDIAPPEPKSVEDTGLKMGILSDIALKYLYYVGTGTGMGIADEMRLPWPGVIEHVVDFLATEKLVDLRGGKGFGRASVEFILSEKGREYARDALTRTTYVGPAPVPIEQYNALITSQTEETPVVSQEELVMALSHLTVPAELMDKLGPAVNSGRSLFLYGSPGNGKTSLAEAVSNMFGGEVFVPHCLEIGNQIIQVYDRLIHTPVSLEVGRDTSGRRQTFEMDNRWLVCRRPSVVVGGELTLAMLDLIYSESTRFYEAPFQVKANGGMLLIDDFGRQKVHPTDLLNRWIVPLEKRVDFLTLHTGKKFEIPFDQLLVFSTNLDPKELVDEAFLRRIKYKIEVGNPDEEAYREIFSRVCEAAGIPYVDQAVTYLIEHYYKPRSMELRSCHPRDLVSLIRDAARYRQIPPALSKDLLDQACEVFLVNL
>NZ_CP022203.1|WP_043712923.1|3512767_3513610_-|Fic-family-protein
MKERYQDIDEKNETLRGYLDIYKDKPDAREFMDKMEMSWIYHDAALEGVVYTHQELMAALFPHRTSAEASMIPVVLEIRNHKAVCDYIREEAAGARKQAQITLTTIKRMHDLFLGNTPEAQTERARMERRERTEKELAKERDRSGLRKDMPLHRTYFHDIAQPAKIQPELEKLVDYTASAEFREFHPIKQAATVQHKFVQIFPFTEHSGKVGRMCSNLILLRNGYMPAVIHSIDRQRYYESFRGPAAAFRTVLMDAMENSLDNGMKYFRDLGRKYKALNG
>NZ_CP022203.1|WP_095958561.1|3511492_3512614_-|DHH-family-phosphoesterase
MPVTQSLNSRRGAGNSGGELTEPPPARLAHMPARDKLERLLRVAQGHHKALILTHDNPDPDSLAAAVALAHLLEHKAGMEAHVGYGGIIGRAENIAFVKVLRLPVSHVSTLDLDEYDLFGLVDTQPKVGNHSLPAKKEAHVVVDHHPLRQESLEAPFADVGGDFGATSTMLVEYLRAARLEPSVEVATGLFYGIKADTRDLGRETTPTDVDSYLWLFPRMDKTLLAQIEHPELPARYFQLYHTAYERAKVYGTAIVTDLEEVYSPDMVAEVAERLMFLEGMKWSLAFGTYRNQLFLSLRVKDRRMNAGRLIREICEDYGGSSGGHGSMAGARLPLSGKLAQRKALKRELVGKFLEAFGVSDERPVSLLYAQDS
>NZ_CP022203.1|WP_095958560.1|3510350_3511496_-|cysteine-desulfurase
MTYWDYNAAAPVRPEVVALLSRAFASGGFGNASSVHQEGRAARARLDAARVKVARVLGCEPKEVSFTGSGSEADALALLGAWYARPRPERRRVVTSAVEHPALLGAAARLEREGAHVVRVAPGPEGRVREAEVLEALTPDTALCSLMWANNETGVLQPAREVARACRQRGVLFHTDAVQAAGKVPLSLREVDADLLSLSAHKFGGPPGVGVLMVRKRVDVQALTPGHQEGGRRGGTQNVPYAEALALALELAVAELPETAARLTALRDAFEREVAARLSGVHVNGGDAPRVPNTSNLRFDAVEGESLLMALDLEGICVSSGAACASGTLSPSHVLRAMGLSAAQARGSLRFSLGPGTTEADVTRVVEALVRHVPSVRALAG
>NZ_CP022203.1|WP_095958567.1|3529397_3530987_+|DUF1957-domain-containing-protein
MSLGSLALVLHAHLPFVRHPEHEDFLEEDWLYEAISETYLPLLQVFDALAEDGVPFRLAMTLSPTLVSMLRDELLMSRYARRLDLLCELGAREVHRTRDDATFGPLAHFYRDHFESLRRAFHDRYRRDLVSAFRRLQDAGHLDILTCNATHGFLPLMQQVPEAVRAQVTVAANHYRQHFGRDPAGIWLAECGYYPGLERLLANERIRYFFVDTHGLTDAVPRPLHGPYAPVFTEAGVAAYARDPESSQQVWSTEHGYPGDPDYREFYRDIGWDLDLDYIRPFIQPTGERKNTGFKYYRITGKTNEKRPYDPRAARERAAVHAGNFLFNRQRQIEDLASRLGGRAPVVVAPYDAELFGHWWFEGPQFLDFLIRKAAREQQTFRLVTPSDDLREHPENQVATPPLSSWGAGGYATMWLDGSNDWIYRHLNQCAKQMVELARDFPDANELQRRALNQAARELLLAQSSDWAFIMKTGTMVEYAQRRTREHILRFQRLHEQLRGGSLDERWLSQVEGRDNLYPELDYRLYLPA
>NZ_CP022203.1|WP_095958568.1|3531084_3532560_+|trypsin-like-peptidase-domain-containing-protein
MNRSTVSFRKALVAALLVALPPAAVAQAPKPPAATQPGAGNVLQPATREAQTLPSLAPLVESVKSAVVNVDVQARGGGLPRGMEGNPLFDRFFGGGREGGSQRREPLRQGAGSGFIIDPKGLVLTNNHVVEEAVSITIRLDDGRSFSGEVVGRDPLTDVALVRLKEKVEGLPTVKLGDSDALRVGDWVVAIGNPFGLASSVSLGIVSARAREIGASQYDEFLQTDAAINPGNSGGPLFNMKGEVVGINTAIVGGGSGIGFAVPSTLISSLLPQLQKEGSVTRAWLGVGIQDLTRDLANALKLPVNEGAILTQVMPASPASKAGLKQDDVVIAIDGRTVTSSGELTRTVALKRPGSTSTLTLFRDGKKRDVKVALGTRPDLEGVASAKQRPEDQQESSRRVGVSLQNLDARTAKQAGFTDSSGALITDVIPGSPADRAQLEPGMVVIEANRKKVESADALASIIKGAASGSTLLLRVTAPGGARNLRALRVP
>NZ_CP022203.1|WP_013939570.1|3532744_3534679_-|diguanylate-cyclase
MPLGPDTVGRKLLWSIALPGLLVALLGVGHFWREARVAVQDATQVESLALAEFVASTFTLPQARGAPAHGAVTEVLRSDTRLFRSVEDVRVLTLDGRILWSRRTGEEGTVHPEAARLTAPGPERARSVARMTEVIRPLGGPECAGCHTTGDVPGASILQLRMAEPALHQQLSSVFGAALGSMGLFVVLLALITGLALHFILTRPLRRLSAAMRRAEAGDLLVRADARGTDELARLGAAFNQMLARLTSMKAEEIDTHRDLELVKEKLALKDELEDRLKELALLFDVARSLNATLELDELLDAVTRLVTERLRIPEFSIMLMNPDGVLEIKHAWPEGRGAEGLTFALGEGACGRAAESRKAVYLPDTADRSSVFARPDLVKGGLNSGALLAAPMVHMETLLGVMNFQRPEVASFSAEEIELLTAVADVVATAVKNARLHAETVKLTMTDPLTGVPNRRHLFQRMELELARANRFGTPLALLMVDVDHFKRINDLAGHRVGDETLRRVCDVLRLRVRKVDTLARYGGEEFVLLLPQTPRAEAMEVAEKLRRAVAESVALAQPGLPGNHVTVSIGVSHFPSDATAQEELVDCADAALYFSKRTGRNRTTLYEAGMELHPGRERGPHTPSAEPPAVAAPKPPGGVAKA
>NZ_CP022203.1|WP_013939572.1|3535702_3536548_+|tetratricopeptide-repeat-protein
MPARSVIFRLLAAAPLCALSACATTAPAEAEVAALRSELRTLRASQERLQDRVARLEAHEAVSRASASAEVPAARPVPVKVEASPAESLSATPELAVVKLKPRFEPAPRLPTAVAVVEPDDEQVELFISPVAEDAGASGGATMVAAGDDAGEEKDPDLLQAEFDKLVNMLRTGNVEGGVERLQRFAAENPRHPRADNALYFSGLGQMGLNEFKGAAVTFQRLIDSYPAGDAMLDGMLRLAECQMRLNQAADAKVLYTRVVTQFPGTAAATQAEQRLAALPQ
>NZ_CP022203.1|WP_095958569.1|3536544_3537780_+|LysM-peptidoglycan-binding-domain-containing-protein
MKLLSKGRPAMRSRILTSLMLSLAVVPAAHAQQENEEEQDTGSEMDSAEVMDEAPDTAPPTSVAIPPGAPQGRESSPGTVHSVETGDTLWDLSQRYLGSPWYWPKVWSYNPEIANPHWIYPGNQVRFFGAGEEVPTQVSEMVVEEGDLTAPTEFASNDQVTVTGKIGFDAASSVPVTTQGFVTQRELDEAGRIEGSPSNAVMLSFPDSVYVRFKRKGDVKVGDRYVVFHTTQAVKHPINGRPLGYLTDFVGTLRVQRVGDGIVTAQIMDTWDGIERGDLVGPVGERLTERVARRPNAKQVDGTVITALVPYLTIMGENNSIVIDRGSADGVELGNTFTILRKGDPSRHVLGHDVRKPSKAEKAFPWRSIGECMVTELKERTSNCLMTRSLEELVPGDRAYMAPGAGPSASR
>NZ_CP022203.1|WP_095958570.1|3537918_3539040_+|DNA-protecting-protein-DprA
MADAETDSLTAEQQACLALWAVPGLGPRTLAALRAFADGSLAPLAATPVRDWVSQAPVSAQVRRRLASVERLSPVAWRVWEACQASGMKVAFQGQPGFPERLAEVEDAPPLLFYRGAPGLPRRRLAMVGSRHPDQGFLPFARRFAQQVAESGVGVVSGAAAGVDRACHWGALDAGGETWAFLGSALDALDTAQARLLPHFLARGGMFFSELPPGVRASTTTFPRRNRLISGASDAVLVLRAGTKSGSLYTAEAGRAQGRPVFAMPGDVRHEEAAGCNALLRDGRAATCLGPEDVWRALKIDPLAAVPPGTMGAWEDLSAEAKGAFSLLDRVPRSFDEVLVGSTFSPAALVSALVELELTGLVIQHPGRLYERI
>NZ_CP022203.1|WP_013939575.1|3539051_3541613_+|type-I-DNA-topoisomerase
MATRTKKKVEETEAAEEKAPAKKAAAKKKPAARKKTVAKKKTAARRRTKKGDEDALPTVEADAEEEATPRGKGPHYLVVVESPAKAKTIKKYLGSGYTVKASVGHVKDLPKSKMGVDVEHDFQPEYTVIKGKEKVLNELKKMAKSADRVFLATDPDREGEAIAWHIKEELAHPDALRVTFNEITKKAIQEAIAQPRQLNQDNYDSQQTRRILDRLVGYQISPLLWKKVRRGLSAGRVQSVAVRLIVEREEEIKAFVPEEYWTLDALLEGPSGPPPFKAKLSKVDGKKVELKDRATTEGLVAELQSASFSVAKVDRRERRRNAPAPFITSKLQQEAANRLSFTAKKTMTLAQRLYEGVPLGDEGQTALITYMRTDSTRLSDDAVKQVREFIDGKYGKDFLPDEPMVYRSKKSAQDAHEAIRPTSLEYPPERVKGFFEAMGEEDMYRLYELIWNRFVACQMKPAVYDQTSADIAAGRATFRASGSTLKFAGYLAVYGAGLTPEEEAEKEKAKAAGDENAEGADAVGELPVLNDGDALNLQKLLHEQHFTQPPPRFSEATLVKELEERGIGRPSTYAAILSTIQDKKYVEKLEGRFRPTDLGNMTNEMLVKHFPHELDVTFTATMEEKLDQISEGGANWKSVLHDFYGPFKETLEKAEAEMRDVKREEIKTDIPCEKCGNLFVIKFGKMGHFLACSNYPDCKNTKDFKRDAEGKIVMVEEETTDELCEKCGKPMVIKRGRFGRFLACSGYPDCKTSKPISIGVSCPECKEGYLTERRSGRGKIFFGCNRYPDCKFAAWDRPLAEPCPTCASPYLLQKFSKRDGPYVACPNKECDYRREITEQPAGPGGSPEASSAA
>NZ_CP022203.1|WP_013939576.1|3541774_3542512_+|MotA/TolQ/ExbB-proton-channel-family-protein
MIPSVSELLLDVTFAATEGGQMGVTDSVIKFFKDGGPFMFVNLFWLACSLAVALERVVTLVFRYNLNAPPFMEQIAKLVRSGNLDRAVKVCAMAPNAPLAKVVRAGLVNANRGEIEVSKAVEEAIVEHSPHVSKRIPWLWSLANIATLVGLVGTIFGLIGTFQALGNVPAEQKQVLLSDGISKAMNNTAFALSIAVICIIFHLFLTSYAKSMVEGMELHALKLENLLSRRGAVDPATTELEARAS
>NZ_CP022203.1|WP_095958571.1|3542531_3543053_+|biopolymer-transporter-ExbD
MAFHYSRRKLKVREEEETGELNIVPYLDILMNLIIFMLLSITGLATFGIINVNAPAYGAPTTGMAQEDPDDAPKLTLSVLISKKGHFVSSENAILGEAGTPTIPVKADGMHDFGALNAKMVEIKSAFPKETKVIVGADPDVPYETLTQTLDAIRETQGRERRLLFPDVTLGAI
>NZ_CP022203.1|WP_095958572.1|3543055_3543637_+|biopolymer-transporter-ExbD
MADPTSPALDTPDAETVARLSYRRALARKKRKEREAAGEIKELNITAMMDMMTILLVFLLKSFASSSAAVTASEDVRPPVSSTRATPRDTVAVTITPKNVLVGDKEVLRLQDGQFPADKLQGRLVLPLDAQLKKEVEKLKYIAARNPSAPFSGELSVIADKKIPYDMLLTVLYTAGQNELENYRFVVLQKEGE

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Crispr_ID: NZ_CP022203_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_7

4664379-4664534

Unclear

Consensus_repeat	Method
CGGCGCTCCGGGCGGCCCGCGCCA	CRISPRCasFinder

2 spacers

cas3

The CRISPR arrays of NZ_CP022203_7

>merge|NZ_CP022203|7|4664379-4664534|CRISPRCasFinder
CGGCGCTCCGGCCGGCCCGCGCCACGGCTCCGGGGGGCGTCTCCCTCGCCGCTGCCCCAGGTGCGGCGCTCCGGGCGGCCCGCGCCAGGGGCTCGGCTGCGCGGCGCGGCGTCACCACCCGCGCTCCACTCACGGCGCTCCGGCCGGCCCGCGCCA

>NZ_CP022203|7|6|4664379-4664534|CRISPRCasFinder
CGGCGCTCCGGCCGGCCCGCGCCA	CGGCTCCGGGGGGCGTCTCCCTCGCCGCTGCCCCAGGTG
CGGCGCTCCGGGCGGCCCGCGCCA	GGGGCTCGGCTGCGCGGCGCGGCGTCACCACCCGCGCTCCACTCA
CGGCGCTCCGGCCGGCCCGCGCCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_043711330.1\|4670864_4671800_-\|site-specific-tyrosine-recombinase-XerD	unknown	unknown	gnl\|CDD\|274043
NZ_CP022203.1\|WP_013940472.1\|4674808_4676032_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366411
NZ_CP022203.1\|WP_043713379.1\|4657982_4658669_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959103.1\|4654179_4656528_-\|DEAD/DEAH-box-helicase	cas3	mkCas0139_cas3_CAS-I	gnl\|CDD\|274800
NZ_CP022203.1\|WP_095959111.1\|4671845_4672826_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959104.1\|4658987_4659686_+\|general-secretion-pathway-protein-GspE	unknown	unknown	gnl\|CDD\|274186
NZ_CP022203.1\|WP_013940464.1\|4666312_4667302_-\|SMC-Scp-complex-subunit-ScpB	unknown	unknown	gnl\|CDD\|377219
NZ_CP022203.1\|WP_095959105.1\|4659724_4661761_-\|cyclic-nucleotide-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|237999
NZ_CP022203.1\|WP_095959113.1\|4673513_4674812_-\|cation:proton-antiporter	unknown	unknown	gnl\|CDD\|223551
NZ_CP022203.1\|WP_095959112.1\|4672848_4673460_-\|threonylcarbamoyl-AMP-synthase	unknown	unknown	gnl\|CDD\|223088
NZ_CP022203.1\|WP_095959102.1\|4652481_4654164_-\|ribonuclease-H-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|379215
NZ_CP022203.1\|WP_095959101.1\|4650818_4651796_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959108.1\|4667288_4668158_-\|segregation/condensation-protein-A	unknown	unknown	gnl\|CDD\|234635
NZ_CP022203.1\|WP_043713373.1\|4651879_4652362_-\|peptidylprolyl-isomerase	unknown	unknown	gnl\|CDD\|223976
NZ_CP022203.1\|WP_095959106.1\|4661760_4663881_-\|HEAT-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|237512
NZ_CP022203.1\|WP_013940473.1\|4676064_4676403_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_043713376.1\|4656718_4657966_+\|citrate-transporter	unknown	unknown	gnl\|CDD\|238537
NZ_CP022203.1\|WP_095959109.1\|4668318_4669365_-\|tryptophan--tRNA-ligase	unknown	unknown	gnl\|CDD\|234866
NZ_CP022203.1\|WP_013940453.1\|4649898_4650819_+\|bile-acid:sodium-symporter-family-protein	unknown	unknown	gnl\|CDD\|223462
NZ_CP022203.1\|WP_095959110.1\|4669649_4670822_+\|DUF4388-domain-containing-protein	unknown	unknown	gnl\|CDD\|373017

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_043711330.1\|4670864_4671800_-\|site-specific-tyrosine-recombinase-XerD	gnl\|CDD\|274043	TIGR02225, Tyrosine_recombinase_XerD, tyrosine recombinase XerD. The phage integrase family describes a number of recombinases with tyrosine active sites that transiently bind covalently to DNA. Many are associated with mobile DNA elements, including phage, transposons, and phase variation loci. This model represents XerD, one of two closely related chromosomal proteins along with XerC (TIGR02224). XerC and XerD are site-specific recombinases which help resolve chromosome dimers to monomers for cell division after DNA replication. In species with a large chromosome and with homologs of XerD on other replicons, the chomosomal copy was preferred for building this model. This model does not detect all XerD, as some apparent XerD examples score below the trusted and noise cutoff scores. XerC and XerD interact with cell division protein FtsK. [DNA metabolism, DNA replication, recombination, and repair].	3.20726e-135
NZ_CP022203.1\|WP_013940472.1\|4674808_4676032_-\|hypothetical-protein	gnl\|CDD\|366411	pfam00999, Na_H_Exchanger, Sodium/hydrogen exchanger family. Na/H antiporters are key transporters in maintaining the pH of actively metabolising cells. The molecular mechanisms of antiport are unclear. These antiporters contain 10-12 transmembrane regions (M) at the amino-terminus and a large cytoplasmic region at the carboxyl terminus. The transmembrane regions M3-M12 share identity with other members of the family. The M6 and M7 regions are highly conserved. Thus, this is thought to be the region that is involved in the transport of sodium and hydrogen ions. The cytoplasmic region has little similarity throughout the family.	0.00070318
NZ_CP022203.1\|WP_095959103.1\|4654179_4656528_-\|DEAD/DEAH-box-helicase	gnl\|CDD\|274800	TIGR03817, DECH_helic, helicase/secretion neighborhood putative DEAH-box helicase. A conserved gene neighborhood widely spread in the Actinobacteria contains this uncharacterized DEAH-box family helicase encoded convergently towards an operon of genes for protein homologous to type II secretion and pilus formation proteins. The context suggests that this helicase may play a role in conjugal transfer of DNA.	0
NZ_CP022203.1\|WP_095959112.1\|4672848_4673460_-\|threonylcarbamoyl-AMP-synthase	gnl\|CDD\|223088	COG0009, SUA5, Putative translation factor (SUA5) [Translation, ribosomal structure and biogenesis].	4.37118e-67
NZ_CP022203.1\|WP_095959104.1\|4658987_4659686_+\|general-secretion-pathway-protein-GspE	gnl\|CDD\|274186	TIGR02538, Type_IV_pilus_assembly_protein_PilF, type IV-A pilus assembly ATPase PilB. This model describes a protein of type IV pilus biogenesis designated PilB in Pseudomonas aeruginosa but PilF in Neisseria gonorrhoeae; the more common usage, reflected here, is PilB. This protein is an ATPase involved in protein export for pilin assembly and is closely related to GspE (TIGR02533) of type II secretion, also called the main terminal branch of the general secretion pathway. Note that type IV pilus systems are often divided into type IV-A and IV-B, with the latter group including bundle-forming pilus, mannose-sensitive hemagglutinin, etc. Members of this family are found in type IV-A systems. [Cell envelope, Surface structures, Protein fate, Protein and peptide secretion and trafficking].	4.95808e-23
NZ_CP022203.1\|WP_013940464.1\|4666312_4667302_-\|SMC-Scp-complex-subunit-ScpB	gnl\|CDD\|377219	pfam04079, SMC_ScpB, Segregation and condensation complex subunit ScpB. This is a family of prokaryotic proteins that form one of the subunits, ScpB, of the segregation and condensation complex, condensin, that plays a key role in the maintenance of the chromosome. In prokaryotes the complex consists of three proteins, SMC, ScpA (kleisin) and ScpB. ScpB dimerizes and binds to ScpA. As originally predicted, ScpB is structurally a winged-helix at both its N- and C-terminal halves. IN Bacillus subtilis,one Smc dimer is bridged by a single ScpAB to generate asymmetric tripartite rings analogous to eukaryotic SMC complex ring-shaped assemblies.	1.72453e-63
NZ_CP022203.1\|WP_095959105.1\|4659724_4661761_-\|cyclic-nucleotide-binding-domain-containing-protein	gnl\|CDD\|237999	cd00038, CAP_ED, effector domain of the CAP family of transcription factors; members include CAP (or cAMP receptor protein (CRP)), which binds cAMP, FNR (fumarate and nitrate reduction), which uses an iron-sulfur cluster to sense oxygen) and CooA, a heme containing CO sensor. In all cases binding of the effector leads to conformational changes and the ability to activate transcription. Cyclic nucleotide-binding domain similar to CAP are also present in cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) and vertebrate cyclic nucleotide-gated ion-channels. Cyclic nucleotide-monophosphate binding domain; proteins that bind cyclic nucleotides (cAMP or cGMP) share a structural domain of about 120 residues; the best studied is the prokaryotic catabolite gene activator, CAP, where such a domain is known to be composed of three alpha-helices and a distinctive eight-stranded, antiparallel beta-barrel structure; three conserved glycine residues are thought to be essential for maintenance of the structural integrity of the beta-barrel; CooA is a homodimeric transcription factor that belongs to CAP family; cAMP- and cGMP-dependent protein kinases (cAPK and cGPK) contain two tandem copies of the cyclic nucleotide-binding domain; cAPK's are composed of two different subunits, a catalytic chain and a regulatory chain, which contains both copies of the domain; cGPK's are single chain enzymes that include the two copies of the domain in their N-terminal section; also found in vertebrate cyclic nucleotide-gated ion-channels.	7.74472e-26
NZ_CP022203.1\|WP_095959113.1\|4673513_4674812_-\|cation:proton-antiporter	gnl\|CDD\|223551	COG0475, KefB, Kef-type K+ transport systems, membrane components [Inorganic ion transport and metabolism].	5.23223e-12
NZ_CP022203.1\|WP_095959102.1\|4652481_4654164_-\|ribonuclease-H-like-domain-containing-protein	gnl\|CDD\|379215	pfam13482, RNase_H_2, RNase_H superfamily.	1.40174e-48
NZ_CP022203.1\|WP_095959108.1\|4667288_4668158_-\|segregation/condensation-protein-A	gnl\|CDD\|234635	PRK00104, scpA, segregation and condensation protein A; Reviewed.	1.61093e-64
NZ_CP022203.1\|WP_043713373.1\|4651879_4652362_-\|peptidylprolyl-isomerase	gnl\|CDD\|223976	COG1047, SlpA, FKBP-type peptidyl-prolyl cis-trans isomerases 2 [Posttranslational modification, protein turnover, chaperones].	2.18503e-49
NZ_CP022203.1\|WP_095959106.1\|4661760_4663881_-\|HEAT-repeat-domain-containing-protein	gnl\|CDD\|237512	PRK13800, PRK13800, fumarate reductase/succinate dehydrogenase flavoprotein subunit.	5.23352e-08
NZ_CP022203.1\|WP_043713376.1\|4656718_4657966_+\|citrate-transporter	gnl\|CDD\|238537	cd01117, YbiR_permease, Putative anion permease YbiR. Based on sequence similarity, YbiR proteins are predicted to function as anion translocating permeases in eubacteria, archaea and plants. They belong to ArsB/NhaD superfamily of permeases that have been shown to translocate sodium, sulfate, arsenite and organic anions. A typical ArsB/NhaD permease is composed of 8-13 transmembrane domains.	3.31262e-87
NZ_CP022203.1\|WP_095959109.1\|4668318_4669365_-\|tryptophan--tRNA-ligase	gnl\|CDD\|234866	PRK00927, PRK00927, tryptophanyl-tRNA synthetase; Reviewed.	5.08803e-155
NZ_CP022203.1\|WP_013940453.1\|4649898_4650819_+\|bile-acid:sodium-symporter-family-protein	gnl\|CDD\|223462	COG0385, COG0385, Predicted Na+-dependent transporter [General function prediction only].	1.25751e-56
NZ_CP022203.1\|WP_095959110.1\|4669649_4670822_+\|DUF4388-domain-containing-protein	gnl\|CDD\|373017	pfam14332, DUF4388, Domain of unknown function (DUF4388). This domain family is found in bacteria, and is typically between 102 and 135 amino acids in length.	0.000192804

>NZ_CP022203.1|WP_095959106.1|4661760_4663881_-|HEAT-repeat-domain-containing-protein
MRTGARPLILALALLLGCNGSRDQLLADLQSPRPEVRALAVKKLAGQGNPDDLVLFTRAAKDFAAIVRAEAAVALGESQDARVVDLLGELLEDADEEVQGRAAMALSKVNNEKAKAYLTLQYGRRGRATRRIIVQALKNANVPGAMAEVVAAEARSQWDRNQLALTEGALPERVGAAEELGKSGRPDAVNRLLPMVRDSQVILAAAAVRGLGDAGDKRAVGPIALLLEENFPELRESAIHALMKLQDPVATQRLQLVAVEKSAVSPLATDAIVSFPRTPQTDAALCAIVLEGAPAEALVAGRAMRARGGCPVDPIGERLARPATAVGGLQAITGLGPTALPLLGKVVPWLSHPDASMRLLAVEAVAELGDASVVPAVQKLYEQESKGLEALRADWVTQALPEKFGLGFDPSTMPPTQTMPGMNDDRPSRHADLLGRVKELNAARVRESGRDVVRHRVPTELYDDVAAERLVPLATLLRALGTLKAPGALELLTGYTQDSSPALRVAALVGLARLGPEGVAVAKAGLIDPDRDLQKALAQALADAGEAGQAALIELLPKMGSEKLLALDALTRGSGVPASASAPLQAVVREGGPEAALAAALLGRLQAKDAVPTLVKALDEPNSVARRDVLLALGSIGDAQAADAVAKDLFHDMPEIRAAAASSLRKLGSAAHADPLEALKGDYFRTVREAAGAAPLSESTASEGAR
>NZ_CP022203.1|WP_095959105.1|4659724_4661761_-|cyclic-nucleotide-binding-domain-containing-protein
MELRKLKDKATEAFTKGRFSKAAELYEDYCRAEPKDHQSRLRSGDAWVKAGQKDRAISAYQAAAEGFARDGFLPRAIAASKLILELDPAHRGVQQMLADLYARRGTPAGARVRGPMSSASAVTKPEAPAARSGGGDGASPAPLAARGPAVDVSSEPPPELALSANEPSSGHEEVVHSVQIGLAHDEASAGVELTLDIATSTAAVPPESRPEPTAMPASEPVTPPLATRLPAVQPGGARAATSALPPGLAPRASQRVPAVGAPRASEPEAPTPRPVSNSGRWQALASPISEQPPTAPVPSTVDASASSAPPGLRPRRAEQAAPAGASVLPVHDLSSALGASLRTASSPSSFTELELEADSLLHAVELAAQAGLHRQGLAAPASSDGVEEELDSLTEEAPADAASLDTLPTIPLFSDLPRDAFIELFERCPLRRFGPGERIIQQGSHGDAFYVICEGAVRVFRTENGARQDLATLEGGTFFGEMALLSGAARTASVESASEDTQLLEISAGVLAELSRSHPQVAQALKKFCRQRMLTNVMNTSELFRLFGRSDRRALVERFRSRDVERDTVIIRDGDPTDGLYVVLSGEVEVRKDGHLLTQLREGEVFGEISLLQKTPATATVTATRHTTLLRLPRADFDTLISSHPQILALISDLSDERLRRTQRVLTEAGVEEDLILV
>NZ_CP022203.1|WP_095959104.1|4658987_4659686_+|general-secretion-pathway-protein-GspE
MDAGLLSETQLRSALAEQRKWGGKLGLTLVHMGYVDESSMVHALSRQLAIPTVDLEQHTPAPLALQALRADIAERYTVFPIAADPATKTVTVATADPTNVEAFQELAFHSGQRLQVVVASASSIERAIRRHYHGEVTSTTATPLSFGMDEPTFELAPPAESEPLSVAVRAASAALAQPGREAELAQRVEELTQQVAGLERMVAQQARSLRAMLELLETRGLVTRDDYLAKVR
>NZ_CP022203.1|WP_043713379.1|4657982_4658669_-|hypothetical-protein
MFREDSAYGDKLKKLEPVEADRRLTVKLLQAVTRFEVSERLRVNTLTQLPREFPWTHVVDPARVASVLESFLVEEVPANAPDYDLVASLGADTIVEFVIEDYGMRSDDGHAGAYLRGYGRMFTLDGRTEVWRRPFDLDQVTQGKPHLDPFKVGKNPSLFRDAMTELLDEVAQLFVKDLTPQDRGAAPPPSRASAASDVVPGQAGAPAPEAEKPAEDTLAPGELPDPDP
>NZ_CP022203.1|WP_043713376.1|4656718_4657966_+|citrate-transporter
MALAIFLFTYVFIAGARLPYLKLDRPGGALLGAVLMVVFGVVTPAEVYNHSADANRHAIDADTIVLLLGMMLLAAYMSQASFFRTAGAWAVRKAHTPRLLLLAVTFISAALSAFLVNDTVCLMLTPLVLATVEDARLPPAPYLLAVCMGSNSGSVATFTGNPQNMLIQGASGLSYASFAAYMALPALLSTAVVAAGLLYLFRHDLPSKRFEPNPPPPPVDRGLMALTLGVLTGVVVAFFAGLPMSWSALAGAALVMALARREPREALERVDWVLLLFFASLFVVVYGVNKHGWAEEIRVLFEPLMTGPPLREMVGFAGLTLVASNLFSNVPFVMLARTWVPTLHDAELGWHVLALGSTLAGNLTLVGSVANLIVFEAARGKVNMTFLRYLRVGLPVTLVSFVVGLTVLLLEHALL
>NZ_CP022203.1|WP_095959103.1|4654179_4656528_-|DEAD/DEAH-box-helicase
MSAVLEGWRSDRQLRSCFVLDEATPARAGVFAPIPEEVAPQVREALEKRGVQQLFSHQAEAYRLARAGRSLVIATPTASGKSLCYNLPLLDRFAREPQARALYLFPTKALSRDQEESLRALMREAGLSHGAITFDGDTPADARRAARERSGVLLTNPDMLHTGILPHHASWARLFSNLRYVVIDELHTYRGVFGSHLANVLRRLQRVARFHGADPVFIAASATIGNPEAHARRMLGRDVTLVSESGAPSGERRVMVFNPPVVNAELGIRASYLKTAVRLTADLVRAGVSTLLFGQSRNNIEVMLKYLRDRFVEEKLDPSLIQGYRGGYLPGTRRATEAALRAGEVRCVVATNALELGIDIGSLDAVVCAGYPGSVAALMQRFGRAGRRGEGSLALLVTSSAPLDQYLAGDPRFLVGSPVEHARIDPDNVEILVQHLKCASFELPFEEGEPFGDVPPESTTEALGFLAQHEVVHPTIGEAGRRVFHWSTDAYPANHVSLRSVGWDNVVIIEKGTDRTLAEMDFRSAHTMLHEQAIYQHEAEQYQVERFDYENHKAFVRKVAPDYFTDAMTYVRVHVIQEDQAAPIGPDLQAGMGEVSVIEKVVGYKKIKYHTHENVGYGDVALPEMQMHTTALWLTVPETVVRAMRAPRPAVIDALRGLTTALRTVACVGLMIDPRDIGKTLGSRDDAEGPPRKDGGVGFDPTLFLYDNVPGGVGLAARLYDQRDELLNRARRLLESCACEDGCPACIGPAAGAMPGQAPVDPHPRKRLALEVLSALGVAGVQ
>NZ_CP022203.1|WP_095959102.1|4652481_4654164_-|ribonuclease-H-like-domain-containing-protein
MDLKRKLARLTSVGPGGKAPPRPAVAEPRAEEPAGTTAESNVSEALARLAQARRMDEPPSTQAEPGVPAALARLAQARRMEAPSQPDAGDSPTAPAGQGTPAPATIGAEAQVPTSARAHPAPRPSTSSPAPEAAAPRPSDPRIDSLRRLLSDWSERQGQAAARRGTPPPAPPGPLPVESRATAHGTIHVSERIHTPEHRHGSAPVAAALDVEGPLVASLALHADLAGVDFQRMLFLDTETTGLAGGTGTVPFLVGLAWFEGRSLKVHQLFLRRLGEEAPMLRALAERMATSSCLVTFNGKSFDWPLLRTRFVLNRVPAPAELPHLDLLHCARRVFKHRGAGARLVHLEDQVLGFRRVDDVDGSLIPDLYFRYLRGGDGASLTPVLEHNVNDLLLLAALLGELVRRFRAGGAGASVPRGEDPRDLLGFAGVALRARDYERAQAFARAAAAGDTGAVGIEALALASRLSRKAGDAAAAAAHLHQALNTAQGFQAAALHLQLTKLYEHDLKDLARALHHAKLASAAELPADHHRRILRLEARLARSTRAASLDLGMERPRSGT
>NZ_CP022203.1|WP_043713373.1|4651879_4652362_-|peptidylprolyl-isomerase
MKITKDSVVSIDFRLHLGDGKAVDESEPGEPLVYLQGHEEIVPGLEKALDGKSRGDTLQVTVGPDEGYGDYDPEGVEEVPKTEFPEGLELVAGGVLSATDPDGDEVDFFIKEVKADSVLVDFNHPLAGKTLHFEVTVRDVRAATAEELEHGHAHGPHDHH
>NZ_CP022203.1|WP_095959101.1|4650818_4651796_+|hypothetical-protein
MTLRRPLSVLSLSLCLGFSAPAAAEEAEAEALPSTPQTTPKPTDAPTAPTLPPLGPDTRLYFANINFLRWNPLGMETQNRLVLQKRMFDGESMLTRDNFVNGAFALKANPASMKIGPVLEIQPLAIFNLRATYEYVRYFGTFGFLQSYNNPLLDFSDDARSLTQDDAYSTSGHHYMVEPTLQARFGSFVVRSKTSIEYWNVALREGQGASFYDALLDTLIPGRGWVFTNDTDLMMLTTPQLTLGARFSGVWPRYQDGSGGAQNVDNSHTRIGPMVAYALNTREGSSFNRPTILLNFAWYLNHPNRGGALPYMMGAFAFTSDFLGG
>NZ_CP022203.1|WP_013940453.1|4649898_4650819_+|bile-acid:sodium-symporter-family-protein
MQSNVFTAVLMPLALAVIMLGLGLTLTLADFKRIIVYPRAILVGLVCQMLLLPVACLGIAHAFALPPELAVGLMLLAASPGGATANLFSHLARGDVALNITLTAVNSALSLVTLPLIINLSLMHFMDDGRAVPMQFAKVVQVVLIVLVPVSVGMLIRSRSASAAQRMDKPIRVLSTAFLVAVIGASVYTERENALGFFRQVGPAALAFNLVSLAVGYFVPVLLRLPRKQAVAIGMEIGIHNGMLAIAIALSPTLLANSTMAIPPAIYSLIMYFTAAAFGFYVSRRYADEQSPAVDRTPTSLPEKVS
>NZ_CP022203.1|WP_013940464.1|4666312_4667302_-|SMC-Scp-complex-subunit-ScpB
MTTGSDGPQDETPEPGTPGGPGPFSEEEIAAVTGPGPADELDEFEAASIEEDSDEAPPDLETSFEKLVSKSRKLSTDRIRTVIESVLFVAERPLSVDELYMATGIERELIAEALNQLSGIHRDGISGIVLYEVAGGWQFRTDPHSGEYVRRYLRVKPQRLTRAAVETLAIIAYRQPVTRPEIEDIRGVDCGAVIKALMDRKLVKILGKREEVGRPILYGTSREFLEFFALKDLSALPTLREFHELTQEHREIVEKEDKPAPPAAGTVEALSDPAFTKRMEKSAAASEAALEDLEEAMAAADRTQKVSSSVLDTTPPKPETGDTTGPKPE
>NZ_CP022203.1|WP_095959108.1|4667288_4668158_-|segregation/condensation-protein-A
MSEERRSPADEALREGELPRSPGDNFRIALPNFEGPLDLLLHLIKEHRVDIFDIPLALITEKYLEHLDRMREINLDIAGEFLVMASTLAHLKSRMLLPRQDVVAAQEAGEVLSVSEEAEDPRAELVRRLLEYQKYKDAAEQLATQDLLGRDVFARSVPVEAVPIPEDEVGLQEFSVLKLVEALDRVLERLQPKLQHEVVRERVTLSEAILRVVERLRPDGQVLFESLFTEEDTPSRQEVVITFLAILEMVKRRLIRVVQDEPLGPILLLPNGDALEKLAPAEVDDSDYR
>NZ_CP022203.1|WP_095959109.1|4668318_4669365_-|tryptophan--tRNA-ligase
MRILSGVQSSGRLHIGNYYGALRQFVQLQDEGEGYYFIANLHALTTVRDPKAALALTREAAMAYLSLGLDPKKAVLFRQSDVREVLELYWILGTVTPHAHLERAHSYKDKVAKGISPDFGLFAYPVLMAADILLYSADFVPVGKDQIQHIEFARDWAVKFNTQYVPGYDPADPEGKERGHAPGILKLPAARIQEATQTVPGVDGQKMSKSYGNTIELFGDEKEIKKRIMSIKTDSTPVDAPKPVPTQPATTPGLISDAPLYDLLKLMLPESDFAEVDATWKAGGKGYGDYKKKLLEAYHAAFGPARQRYAELAADPGEVERILQDGANRARAEATRLMDQVRKAVGIP
>NZ_CP022203.1|WP_095959110.1|4669649_4670822_+|DUF4388-domain-containing-protein
MEPFNGSLASYRLQLVMPPLFSAPGVEGVLRVERGAVRRCFHVKDGYLVGESSNDPREHLAQVLVNLRILDAPRAAAAFEAAEGAGMPYGTFLVQRCFVELPRLIEALEHKARESLFDCYAWESGEVEFTPGLPPNTRAVGLKLSLSTLHRDAVTRQREWAMFRDIFPRLDTTFRVYREFAVETYSEEEDVLLDLASSGATLGELLASAREAPLFAARWVLHLYRRGALAPRKARGPRLGEAAELAELLTLVKRFLENGKYDHAVALAAQILERGPVPEAHALYREAEIRLTLALSDELFALDGRLVFEPIPRPTPPDLTADDLYLYSKLRGSRSIRQALRTAAMGELAASRSVHRLMATGLIRVAPLPGSEPRRAQTDPFGLPVHVAGS
>NZ_CP022203.1|WP_043711330.1|4670864_4671800_-|site-specific-tyrosine-recombinase-XerD
MEGMLDAFIAFIRAERGLSGKTVDAYAADINVYFEDLRSRGVADVTQVRQEDVSAHLAALGKRGLGKRSQARHLAALRGFHRFLVAERMADKDPTEDLDTPRSARKLPVFLTLDEVEQLLAAPDERTSTGLRDKAMLEVLYATGLRVSELCGLGINDVQLTAGYLVAKGKGAKERLVPLGRVAIEKVQAYLAESRPAVLGKRKSQALFVTPRGSGFTRQGFWKLLKRYALKAGILKPLSPHKLRHSFATHLVERGADLRAVQQMLGHADLATTQIYTHVNAARLRSVYDEFHPRSDVFVPKAKKPRASAAR
>NZ_CP022203.1|WP_095959111.1|4671845_4672826_-|hypothetical-protein
MAQGGTRPSSVDGPEQVPGLLRLLLLLLFRPVDLHYRLRSAGIALPGARLATLNGHAAEGHKATSVYLRRMLLLLLVWAPVVTELLGLALLSAGLPLERGWVLSALCCSAVGLVLAQTLGLAAGVLLGSLASLATLLGLHATAANAFGPDLGGAAGMMVGLCLGGVAGLACGSISGIAIGRGPTVVWVQLAAILTSLTPMAVWSGTTNVSYAGAVAASALVAFLVSAFRLPLYALEVLASAVAYAVERWTGRPTLGWVPVRHHNLSYLPHPFLGRHLALAVRSRPAEVLAVADACLRSPGNIVVGWPWVVQALESAVPEGAGEPRR
>NZ_CP022203.1|WP_095959112.1|4672848_4673460_-|threonylcarbamoyl-AMP-synthase
MAAPILEVDMEHPSPRHIQRAVEVLERGGLLAYPTDTYFGLGCDLSSKKGIERLYQLKGRDKKKPLSFLCPDLSDVARYAHVSNFAYRTMKSLTPGAFTFILEATRLVPDLMMSKQKQVGIRVPDSALVRELARALGRPLVTTSATNTEGEPLTDAKDIKAELGHGLELILDGGVTLNEPSTVISLIGDSLEILRQGKGRLED
>NZ_CP022203.1|WP_095959113.1|4673513_4674812_-|cation:proton-antiporter
MNGSVIRLLLLMVLLAIISRAQVLRADSGTPVILAAGALLLCGLFAGKVAKGMGLPRLTGYLLVGVAVGPHALGFIPNAGVKGLELVKGLAVSLIALVAGTELRLGLIRRVGARVALLCAAVCGFTFLVCFGATFALKPVLPFLTAMTVPQALAVSALMSTVVVSFSPTVTIAIVQETSARGAFTEFLMALVIIGDLFVMVAFALAAGVTKASFGGGLDVPGLLGGVGWELFGSVVVGLVLAVGMLIYMRGVKQELPLFLVGLCFAAAEGGTRLHLSPLLVSLAAGALIANLDEHAGERIHNAIQQAGLPVFALFFAAAGAGLKLDTLVSVGPAALLLVALRGAAIWFSCRRFAPADDPRLKRYLWMGLISQAGVTFGLAALVSRTFPTFGPQVEVLIVAMITAHELVGPVLTRKALAASGEIRSEDAQGTA
>NZ_CP022203.1|WP_013940472.1|4674808_4676032_-|hypothetical-protein
MQALLVFLSIAALSLLASSRALDPGRFPALARLAASGFLFVLLGILLGPSVAGVLTERNVEALRPVMALGLGTAGVLLGLNLEPRLLRLLPRPVYLSAMAHSGTAFFFVALPLLVPLLFTSGRGVLGAVGAAAMLGAAASLSSGHSAVLAWRAGRLDRARGLGVALLTMLDDAVGLGVLALALMIGSADNVGEGLGLVCLALLLGVMCGALLAFLTHGLKDLAELTTVTLGGVALVGGAAAYLRVSPLLAGVACGATLAVVGGRTSERVARALGRVERPVFLVLVFLVGCAVHARDYWAWALMPAYVGLRFLGKMAGGRLASRLVQQTLVLPPRLGYALIAQGGLALCLVAEYGMLVPGVLARRVLDVVVMGAVVNELLAGQAFQHVMEPPRGALTPSSSDGDKVAA
>NZ_CP022203.1|WP_013940473.1|4676064_4676403_-|hypothetical-protein
MYLVITFLEQLEGTERAIRRLREFGIPEPLVVRARSAAAALSAEVPVFAGLRSLALGADDDRVILLSLLPGVPAEEMERLVQRVQLEMDADDPPMGRLVAMPVISAPTHRRS

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Crispr_ID: NZ_CP022203_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_8

4795820-4796003

Orphan

Consensus_repeat	Method
GGTGCCGGCGTCGTCCTCG	CRT

4 spacers

The CRISPR arrays of NZ_CP022203_8

>merge|NZ_CP022203|8|4795820-4796003|CRT
GGTGCCGGCGTCGTCCTCGCCCGTGCCGGCGTCCTCGGTGGTGCCGGCGTCGTCCTCGATGATGATGCCGCCGTCCTCTTCACCCGTGCCGGCGTCGTCCTCGCCCGTGCCAGCGTCCTCGGTGGTGCCGGCGTCGTCCTCGATGATGCCGCCGTCCTCTTCACCGGTGCCGGCATCCTCGTCC

>NZ_CP022203|8|2|4795820-4796003|CRT
GGTGCCGGCGTCGTCCTCG	CCCGTGCCGGCGTCCTCGGT
GGTGCCGGCGTCGTCCTCG	ATGATGATGCCGCCGTCCTCTTCACC
CGTGCCGGCGTCGTCCTCG	CCCGTGCCAGCGTCCTCGGT
GGTGCCGGCGTCGTCCTCG	ATGATGCCGCCGTCCTCTTCACC
GGTGCCGGCATCCTCGTCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095959187.1\|4811679_4812729_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379240
NZ_CP022203.1\|WP_095959184.1\|4808034_4808949_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274033
NZ_CP022203.1\|WP_095959175.1\|4792750_4793542_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP022203.1\|WP_095959176.1\|4793545_4794328_-\|exodeoxyribonuclease-III	unknown	unknown	gnl\|CDD\|197319
NZ_CP022203.1\|WP_095959178.1\|4796341_4800724_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|223533
NZ_CP022203.1\|WP_095959172.1\|4788724_4789519_+\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|226119
NZ_CP022203.1\|WP_095959173.1\|4789536_4790394_-\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223377
NZ_CP022203.1\|WP_095959171.1\|4785514_4786861_+\|(2Fe-2S)-binding-protein	unknown	unknown	gnl\|CDD\|273584
NZ_CP022203.1\|WP_095959181.1\|4802702_4804793_-\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP022203.1\|WP_013940567.1\|4783335_4783839_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959170.1\|4783789_4785280_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|377376
NZ_CP022203.1\|WP_095959185.1\|4808945_4810607_+\|acyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|173843
NZ_CP022203.1\|WP_095959179.1\|4800862_4801831_-\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP022203.1\|WP_095959182.1\|4804921_4805737_+\|WbqC-family-protein	unknown	unknown	gnl\|CDD\|378083
NZ_CP022203.1\|WP_095959180.1\|4801917_4802700_+\|phytanoyl-CoA-dioxygenase-family-protein	unknown	unknown	gnl\|CDD\|368580
NZ_CP022203.1\|WP_095959186.1\|4810931_4811687_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959174.1\|4792215_4792731_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|274907
NZ_CP022203.1\|WP_095959183.1\|4805744_4807514_-\|ATPase	unknown	unknown	gnl\|CDD\|223679
NZ_CP022203.1\|WP_095961629.1\|4790549_4791017_+\|universal-stress-protein	unknown	unknown	gnl\|CDD\|366180
NZ_CP022203.1\|WP_013940570.1\|4786857_4788375_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|223737

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095959187.1\|4811679_4812729_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379240	pfam13527, Acetyltransf_9, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.26746e-07
NZ_CP022203.1\|WP_095959184.1\|4808034_4808949_+\|hypothetical-protein	gnl\|CDD\|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	2.78858e-07
NZ_CP022203.1\|WP_095959175.1\|4792750_4793542_-\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	gnl\|CDD\|153251	cd07989, LPLAT_AGPAT-like, Lysophospholipid Acyltransferases (LPLATs) of Glycerophospholipid Biosynthesis: AGPAT-like. Lysophospholipid acyltransferase (LPLAT) superfamily member: acyltransferases of de novo and remodeling pathways of glycerophospholipid biosynthesis which catalyze the incorporation of an acyl group from either acylCoAs or acyl-acyl carrier proteins (acylACPs) into acceptors such as glycerol 3-phosphate, dihydroxyacetone phosphate or lyso-phosphatidic acid. Included in this subgroup are such LPLATs as 1-acyl-sn-glycerol-3-phosphate acyltransferase (AGPAT, PlsC), Tafazzin (product of Barth syndrome gene), and similar proteins.	1.46593e-53
NZ_CP022203.1\|WP_095959178.1\|4796341_4800724_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|223533	COG0457, NrfG, FOG: TPR repeat [General function prediction only].	2.18941e-07
NZ_CP022203.1\|WP_095959172.1\|4788724_4789519_+\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|226119	COG3591, COG3591, V8-like Glu-specific endopeptidase [Amino acid transport and metabolism].	2.28421e-09
NZ_CP022203.1\|WP_095959173.1\|4789536_4790394_-\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|223377	COG0300, DltE, Short-chain dehydrogenases of various substrate specificities [General function prediction only].	2.03097e-61
NZ_CP022203.1\|WP_095959174.1\|4792215_4792731_+\|hypothetical-protein	gnl\|CDD\|274907	TIGR03991, alt_bact_glmU, UDP-N-acetylglucosamine diphosphorylase/glucosamine-1-phosphate N-acetyltransferase. The MJ_1101 protein from Methanococcus jannaschii has been characterized as the GlmU enzyme catalyzing the final two steps of UDP-GlcNAc biosynthesis. Homologs of this enzyme are identified in a number of bacterial organisms and modeled here. A number of these are observed in proximity to the GlmS and GlmM genes, and phylogenetic profiling by PPP identifies the LEPBI_I0518 gene in Leptospira biflexa as a likely Glm-system candidate. Multiple sequence alignments of these bacterial homologs with their archaeal counterparts reveals significant structural differences, necessitating the construction of separate models. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Central intermediary metabolism, Amino sugars].	0.00998873
NZ_CP022203.1\|WP_095959181.1\|4802702_4804793_-\|GAF-domain-containing-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	5.07494e-49
NZ_CP022203.1\|WP_095959171.1\|4785514_4786861_+\|(2Fe-2S)-binding-protein	gnl\|CDD\|273584	TIGR01372, sarcosine_oxidase_alpha_subunit, sarcosine oxidase, alpha subunit family, heterotetrameric form. This model describes the alpha subunit of a family of known and putative heterotetrameric sarcosine oxidases. Five operons of such oxidases are found in Mesorhizobium loti and three in Agrobacterium tumefaciens, a high enough copy number to suggest that not all members are share the same function. The model is designated as subfamily rather than equivalog for this reason.Sarcosine oxidase catalyzes the oxidative demethylation of sarcosine to glycine. The reaction converts tetrahydrofolate to 5,10-methylene-tetrahydrofolate. The enzyme is known in monomeric and heterotetrameric (alpha,beta,gamma,delta) forms [Energy metabolism, Amino acids and amines].	4.56825e-48
NZ_CP022203.1\|WP_095959170.1\|4783789_4785280_+\|hypothetical-protein	gnl\|CDD\|377376	pfam04519, Bactofilin, Polymer-forming cytoskeletal. This is a family of bactofilins, a functionally diverse class of cytoskeletal, polymer-forming, proteins that is widely conserved among bacteria. In the example species C. crescentus, two bactofilins assemble into a membrane-associated laminar structure that shows cell-cycle-dependent polar localization and acts as a platform for the recruitment of a cell wall biosynthetic enzyme involved in polar morphogenesis. Bactofilins display distinct subcellular distributions and dynamics in different bacterial species, suggesting that they are versatile structural elements that have adopted a range of different cellular functions.	1.03544e-06
NZ_CP022203.1\|WP_095959185.1\|4808945_4810607_+\|acyl-CoA-dehydrogenase-family-protein	gnl\|CDD\|173843	cd01154, AidB, Proteins involved in DNA damage response, similar to the AidB gene product. AidB is one of several genes involved in the SOS adaptive response to DNA alkylation damage, whose expression is activated by the Ada protein. Its function has not been entirely elucidated; however, it is similar in sequence and function to acyl-CoA dehydrogenases. It has been proposed that aidB directly destroys DNA alkylating agents such as nitrosoguanidines (nitrosated amides) or their reaction intermediates.	2.50761e-118
NZ_CP022203.1\|WP_095959179.1\|4800862_4801831_-\|alpha/beta-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	4.54353e-19
NZ_CP022203.1\|WP_095959182.1\|4804921_4805737_+\|WbqC-family-protein	gnl\|CDD\|378083	pfam08889, WbqC, WbqC-like protein family. This family of proteins are functionally uncharacterized. However it is found in an O-antigen gene cluster in E. coli and other bacteria suggesting a role in O-antigen production. Feng et al. suggest that wbnG may code for a glycine transferase.	9.55378e-77
NZ_CP022203.1\|WP_095959180.1\|4801917_4802700_+\|phytanoyl-CoA-dioxygenase-family-protein	gnl\|CDD\|368580	pfam05721, PhyH, Phytanoyl-CoA dioxygenase (PhyH). This family is made up of several eukaryotic phytanoyl-CoA dioxygenase (PhyH) proteins, ectoine hydroxylases and a number of bacterial deoxygenases. PhyH is a peroxisomal enzyme catalyzing the first step of phytanic acid alpha-oxidation. PhyH deficiency causes Refsum's disease (RD) which is an inherited neurological syndrome biochemically characterized by the accumulation of phytanic acid in plasma and tissues.	1.12561e-22
NZ_CP022203.1\|WP_095959176.1\|4793545_4794328_-\|exodeoxyribonuclease-III	gnl\|CDD\|197319	cd09085, Mth212-like_AP-endo, Methanothermobacter thermautotrophicus Mth212-like subfamily of the ExoIII family purinic/apyrimidinic (AP) endonucleases. This subfamily includes the thermophilic archaeon Methanothermobacter thermautotrophicus Mth212and related proteins. These are Escherichia coli exonuclease III (ExoIII)-like AP endonucleases and they belong to the large EEP (exonuclease/endonuclease/phosphatase) superfamily that contains functionally diverse enzymes that share a common catalytic mechanism of cleaving phosphodiester bonds. AP endonucleases participate in the DNA base excision repair (BER) pathway. AP sites are one of the most common lesions in cellular DNA. During BER, the damaged DNA is first recognized by DNA glycosylase. AP endonucleases then catalyze the hydrolytic cleavage of the phosphodiester bond 5' to the AP site, and this is followed by the coordinated actions of DNA polymerase, deoxyribose phosphatase, and DNA ligase. If left unrepaired, AP sites block DNA replication, and have both mutagenic and cytotoxic effects. AP endonucleases can carry out a variety of excision and incision reactions on DNA, including 3'-5' exonuclease, 3'-deoxyribose phosphodiesterase, 3'-phosphatase, and occasionally, nonspecific DNase activities. Different AP endonuclease enzymes catalyze the different reactions with different efficiences. Mth212 is an AP endonuclease, and a DNA uridine endonuclease (U-endo) that nicks double-stranded DNA at the 5'-side of a 2'-d-uridine residue. After incision at the 5'-side of a 2'-d-uridine residue by Mth212, DNA polymerase B takes over the 3'-OH terminus and carries out repair synthesis, generating a 5'-flap structure that is resolved by a 5'-flap endonuclease. Finally, DNA ligase seals the resulting nick. This U-endo activity shares the same catalytic center as its AP-endo activity, and is absent from other AP endonuclease homologues.	5.45835e-152
NZ_CP022203.1\|WP_095959183.1\|4805744_4807514_-\|ATPase	gnl\|CDD\|223679	COG0606, COG0606, Predicted ATPase with chaperone activity [Posttranslational modification, protein turnover, chaperones].	2.25781e-08
NZ_CP022203.1\|WP_095961629.1\|4790549_4791017_+\|universal-stress-protein	gnl\|CDD\|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	6.10113e-34
NZ_CP022203.1\|WP_013940570.1\|4786857_4788375_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|223737	COG0665, DadA, Glycine/D-amino acid oxidases (deaminating) [Amino acid transport and metabolism].	7.43052e-74

>NZ_CP022203.1|WP_095959176.1|4793545_4794328_-|exodeoxyribonuclease-III
MRVVSWNVNGLRSVHRKGFLPWLAGCRAQVVGLQEVRARADQLPDEVRSPPRWKTHFVAAERPGYSGVGLYSRLEPDEVVTVLGVGELDVEGRLQIARFGKLTVVNGYFPNGNGKDRDLSRIPYKLTFYRRLFERLEKPLRDGGRVLVMGDFNTAHQEIDLARPKENRETSGFRPEEREEFDRWIRAGWVDTFRHFNKGGGHYSWWSQRAGVREKNIGWRIDYVLASPAAMAYVRKAGIHPGVLGSDHCPVSVDLDPAVR
>NZ_CP022203.1|WP_095959175.1|4792750_4793542_-|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MFEALMNALLSIWTWIEIGLVALVGFFVQLSLAILTWAFDRKRHVTGRCFRLIGVTAAKLTPFWRFGVHGAVPDRLAPNTVVVSNHESNADPFLISHLPWEMKWLGKASLFKIPVVGWSMWMAGDIPVHRGDRDSATGAMAKCRQWLAKGMPVMIFPEGTRSKTDELLPFKDGAFRLAIEAQADVLPLAVSGTRRALPKHSWRFATSRGLVTVGTPISTKGMTLADVETLKTLAREQILTLRASLMPLTRVDAPEAPGSANAA
>NZ_CP022203.1|WP_095959174.1|4792215_4792731_+|hypothetical-protein
MRASPLAVLVLALSTPALAEDDAKPQKWKVVCATQSKDGSRAVQGTDLVIEAGEQVKDGVAVEGDVIVRKGARVEDVVAIRGRVIVEPGGRVTGSAVSLGGEVRVHKGAAVDGDAIALGGRLKVDQDEAVKGDKVSLSFEIGGRDIVRGFIEGVLDEETGCHIVDEDTQDV
>NZ_CP022203.1|WP_095961629.1|4790549_4791017_+|universal-stress-protein
MATVSRILVPVDLSDGSREVIDYAVKLARPFKASVEVVHAWEPPQYVAPDLLVAAPGWNSQSLEHVAVETATKELTAQVNQGEPPGVPVSQKIVVGEAASTILDLAEQEKCDLIVMGTHGRRGLPRLLLGSVAQKVVARASCPVLTLHVSEQKPH
>NZ_CP022203.1|WP_095959173.1|4789536_4790394_-|SDR-family-NAD(P)-dependent-oxidoreductase
MRPLPIDQGTVLIIGAARGIGRELARLLARRVRTLVLVDRQAQALEPLREELLLNYPTLGVLVESYDVCDPRQVDALLASLEAQFVRVDVLVNNAAEGDQGLYAQEGWERVEAMLRANVWVPALLTHRLLKPMLERGRGGILNIGSGAAQLILPGSAAFAASQRFLDGFTEALRLEVEGQGVTVTRVAPGPLWEAGLEGADGQTPFFHLSLERCAREALAGFERGEPLVYPGLGHRWVMRLLPLLPRGLKRSLGRMALRGLQREQLLLPRQAPAALPVSGEPSPG
>NZ_CP022203.1|WP_095959172.1|4788724_4789519_+|trypsin-like-peptidase-domain-containing-protein
MFPKSVRALFLVGALSACGTEAPPDVPDADGQEPLQSQEADVIVGSVNWVSATTLSGTQRTRSRAVGYLSIPAVGSRCTAWLVARDVIITNNHCIGSSSEASGARVSFNYEDGVSASARVWYNCGTLIRTWASDDMTALRCTATSGRLPGDVYGVLTVASTNAATGASVYVVHQNCDYYTSSGCTPTKKSSPGVVRNANYSSTDLSYDADTLGGSSGSPVLSSSSNQVVGLHHIGLGGNSQGRGTANTGVKATRVKARLAEIGL
>NZ_CP022203.1|WP_013940570.1|4786857_4788375_+|FAD-dependent-oxidoreductase
MSKAMICSCEDVTVDDIRHAVSRGFCDVESVKRYTGFGTGICQGKSCTAAVAALLAKEKALKPAAVVPFTPRQPLYPTELRMMASAPVDESQPPVGGLPQEVDHFPAALRPEGPVPARAKVVIIGGGIMGLALAYNLARAGETDVVVLERGYLCAGASGRNGGGVRMQWGTPSLVELAKRSIGLMKGFARELGINVWLRQGGYIFMAKTKPVAQRLERNVSLHNRFGVPTRLITPDEARGIVPGLTLKDCLVASYNPEDGVIFPWPFLWGYAQGCQKRGVRVETYTDVTGFETSGGQVRKVKTTRGDIACDTVVLAAGAWSPQVAKLVDVKLPNEPHRHEILSTEPLKPFLTPLVSVLDSGLYFSQSMRGEIVGGMGDAKEPAGLNMGSTLRFVSRFAQAVMEQLPQVGHVKVLRQWAGCYDVTPDNNPILGRTPGLDNLLQMSGFVGHGFMMAPAVAERMAKWMATGESDELFTRFNLRRYSDAAGHSREFGSGTLEREDMVIG
>NZ_CP022203.1|WP_095959171.1|4785514_4786861_+|(2Fe-2S)-binding-protein
MRRLPDVPPRGRAITVDLEGESLPAIEGEPVACSLVAAGEPLLARSIKYHRPRGPYCFAGACSHCLMRVDGVPNVYTCRTPARDGMKLERQNAYPSAKVDLFESIDWAFPKGMDHHEMFAGVPVAEQVMAKVARQLAGLGLLPKAPAPALAPARAVRTRVAVVGGGAAGLAAARVLTERDVGFLLIERDDALGGRLAHGAPEAGGPSLDDVHRLSPSSVMTRATALGLYDDEGGRFLAVGTWEADAPRLVKVYSERFLLTPGGHPPTLPFENNDLPGVYAGRAASLLLRRYDVAPETAALVGWGAELHALANLLHERGTKVVAVVDLRDTPPPGAHATAVRGGEPKAHGLRGVSAFSYTREGGGREKVSCDAVLVSVPVSPSFELARQGGAKVPFDEQRGLFVVETDADGRTQAQDVYAAGDVTGGGTAKDAAAAGRRAAQALVGGLS
>NZ_CP022203.1|WP_095959170.1|4783789_4785280_+|hypothetical-protein
MASSGSSAPGPPLPERERTMKILPRILFPALLLGAPLALAQDAAPRADVTASAPSTIDISFRGSLRDALKTIADKGGLNLVVTGDLDSPAEVHLRGVTANQALRTVARAYSLRLDQDGSIYTLRPMTEQEQQAAESGEAPADAAASAPPEAAAPPVAIPPIPPLPDLPDSFPEEARDEMKRAREEMKKARDEVRRSMRRKGSRDVVARGQNLEVKEGQAVESAVVYGGNLVVNGHVKDDAVAFGGNLEVHGRVDGDAHAFGGNVILGPDARVEGDVSAFGGSVERDDDAQVEGSIESFGGAGIGRMVAGEIKKGVREAKDSERHSDDDDGGAGLAGFILTFAVLFGLGFMGQMFFPARMKQLGEEVRRKPVQTGLIGLFGLVAIAILSVVLCIIIIGIPVALVLLMATPLATALGFAAVASELGTRLPVLRGRKTQAVVLALGLLVLMLLGALPIVGPLITVTVAFMALGAVIRTRFGQRPQGMPEPIIPSSDQPV
>NZ_CP022203.1|WP_013940567.1|4783335_4783839_+|hypothetical-protein
MTAHLCPDLEVLFTELEAGEGPALDHAAECEACAAVLEEHRLMENDLYRLADPLPPPTLVASVMARVSTEPVPRRREVWSGLAILLTSMLGGLGYLVMSDQALGRLGTGLASVLVQGRPFVEGVLSGAHALWSTAGLTVACSLAFLLLTSLYGLKRLVGTGPTPSGA
>NZ_CP022203.1|WP_095959178.1|4796341_4800724_-|tetratricopeptide-repeat-protein
MALPALHHARRPAFAATWPSELLDIITARLADEVHADDLRVIVLAPTQDRLRVGVWLGTEWDRYPDVTGSSAAAGFVSLTPWLDELDALSRGERTLPPPAEWTPLAPLYFHDAARNASFLAWWLELHRALVATAIELGTRLLAERFAQPVGVFVSMSGAEAQLVSFCHPRGAPLWPLREHRKEHGYGSAYPSASLEGDTLVLFYPEGEGEDGGPPSIRGWSRAQVVRAGVDRKALHVTARFEGEDFDVRFSAGHTHPRFGGPPPAAIITALVGFFRAGEGLEAGDLPPPPSGAAEVAATLAALPTVEDQRRYATGLARVVGFERLSGLLAGPEVAAPTRAALCRALASDALDAGQWAAALALVEQLPEADRPSWMEARALTALGRWEDVLRVASHDALPERALALGRLGRIDEALPLVDKADAESEALAVLALLRQAQAAATLRAALAEGVREHLLVHVEASPELGPLLRAHRAVEAAVRASRAACERLTPSPFPLEPARVLAVEPATRALIAPLEDEDAASARAYLLAFVERPDGSWWGADKEGTLREYRADGGPKTLATFSPRIDELVAVASGVVAAVGSTLVLLDAAGQARATLQRPLAGDGPMAAQGALLACASGEAIGLYRATGDTLQWLAPLAMPGSSRIGELGFTGPGRLLVRAGRHLALFDVSEPTWPVPLRRWVDDVDFELVATREGAAALTRDEWIWLVEVGEALRGTHKLHLGPSPRAATSDAAPWAFSSRGRVVEVAGEAAREVFLVGEDASRLGPRALTLRGRQGAAVTRDTVLSLSSVEIDAAPFAAYVEALLPRVREWLFGHLEAWARDGVRAPSGEGRAPLGGLVLTWMTGLWAGVRGQPACSVVSLGFDTSEGLPLGAVAPPPPALRAPGASLAEERQTQALEAAREQRATYEQLRVCRALLREAAAAFAHRSPARTFLLALDTEDGLEVLDVLPGGGAAPRLRAADAPRAGRTLRELLSAAEAGMSMPNLVARARRDAAVRADVLSLLEREGHEAAGRLSLELLDVDLEGCARAWLAVAARDVHQGLPGLLALARRGHAEAHARLLGLVDARDTRLALQARVEVGRADEDATVPLLEQHLASPGEGDAVLARALAVVGDARLTRLRAALLSARAQRGADADWLLLPLVRGGWAPDEETVKAGNAARHGESEFIASVFSADVPEGAASAVRQWTAQRIASAVATAGPLWPQEVPLERHRTGWQRFFTLAWPYWESRGLLPRLYEALAGCEGAADAELAYQLLFQGLLRGDPRCAALGRALARNTAHAGRHAEMTRLATLSRLQFGWSLVKARRLTEARQVADAALADAPQDGQVRFFDARVAWLERDDPTAALDRIDQALRIARDAVGRARLLNLYGAALDVLGRHAEALDWFHKAFTANESAVDSHTGKSGDPGMSHAILSNIAEMHWKLGQREEARRHAEQAARRGSTTEVVMEILAETRA
>NZ_CP022203.1|WP_095959179.1|4800862_4801831_-|alpha/beta-hydrolase
MPYRRTTRFVTAPDGTRVAWHTHFGNLREASADTDLASRPTVLLTNGIGSSENFWRYLVGNLEQDHRVVHWNYRGHGSSDESQADGYRIPVHVGDLERVTEAVMARGDGRPPHHVAYSMGVRVLLDLYRRRPDLVPSMTLIAGAPGAFGSGSDTAAARAFLAATRGMLKLATPTLPLTAPLAHAVMASRFAYPLGRMVGALRARAPRADIDEFMRALRRMSPKAYWYTLRGMVEGHAWDVASTVQVPTLIVAASNDLLVPLGEMERMRHIMPHAHWMRVDDAGHAGLLEAGAEIAEAVRVFLVDHGLEPPHAVGEHAPVPPR
>NZ_CP022203.1|WP_095959180.1|4801917_4802700_+|phytanoyl-CoA-dioxygenase-family-protein
MLCVDVERFDITPALAHYAEHGYARLGRVLGDAGLEALRERADDLMLGRVVHPGLFFQPDAATGRYEDAPLGLGWQGPSLDYRKLEKLEKDPRFLAWLENPLFERVARAFLPGDIVLYRAILFHKGQAGGSNLPWHQDGGRLWGITREPELQIWTALDDAPEDGGCLEVIPGSHRGGLVTALGGVVPPDAVAAAHAEARAVPLPARAGEALLIHNHLWHRSGRGRPGLRRRAFSACYMDADVRCVRKKKAPRVFPPVFRR
>NZ_CP022203.1|WP_095959181.1|4802702_4804793_-|GAF-domain-containing-protein
MFGATEQGDRMKFLCLTSDTRHPVVEELRRQGQGVCVTADLVEAGAALGHGPVDVLVVDAADLTKGARWLDTLRTWARPEEPLVLGLAPAATDEALEPLLAAGVDEFLVEPFCAVQVRARRVLLERRVAARRQRRTSEAEARGELERLASIIQAQSDVAMAGFGLDELMRLLCERSRVLCGADGAAVALLEPAADEVNYLVATGSLAPFIGFRLKVEGSLTGTSLVRGEVMRTDDSEADVRVNVTALRQVGARSMICVPLWREGRPVGALNVTSRRPNAFDDRDVRTLELMAGMLGAAMGNAAEAQARQELMAQNTLALGALEESQELFASFMDNIPAVAFMKDEQGRRLWVNARYCRFFGYPPGTDLSQVADLDLMPPASAEQSRRDDEAVLASGRQSITESMIPAPDGAERHWLTYRFIVRERSGRRLLAGVAMDITDRKAMQAQLVVSDRLAAVGTLAAGVAHEINNPLAFVLSNLSFLSGELHALTRELPSGRVAELEEVLRDATDGAHRVRQIVRDLRTFSRGDDEVATAVNVQAVLESAITLARSELKQRARIVRDYREVPLVEGNEGRFGQVFLNLLINAAQAIPPGQPERHEVRLSLETAGDRVIIEVRDTGMGMPPAVRARIFDPFFTTKPVGEGTGLGLSICHGIVTGFGGDISVESEEGRGSTFRVSLPVVRRALEPPPRMPLVG
>NZ_CP022203.1|WP_095959182.1|4804921_4805737_+|WbqC-family-protein
MARRRYPPRVPGIPGVVVAEQPHYLPWVDFHEQLARAGTFVVLDNVQWLRRGWQRRTRVALPHNVPLPPPTEPGFQWMSIPLEAPRRDALIKDLAVDARQPWAREHLRRLVSLYGRRPCFASQVLPRLEPFYDAAARESGPGSLLRVLLASMALFNEPLGLTPNLVLASTLDKQGEDKSARLVAYCRQLGAHTYYSGLGSSLYLQVGLFRDADVRVLWQRFRHPEYAQGRPGRFVHGMSLVDVLSNVPVDEVRRWLEPSPWGPFAPRPPGD
>NZ_CP022203.1|WP_095959183.1|4805744_4807514_-|ATPase
MSLFRRPPSPESGSSSDESSRSVTPVETAVVPPTVPTPVLSGPPRPRVGVTGASAALPPRPPGATTGSRPALPPEPDEPEFPTERRASSAPPERRGVPQAPATLPSVIVAPPEHRERRGPGPSQYAGPDRRGGAAGAGYNGPERRAFRRGEEGGAGPGDRFWPAQPRTLGETGLNTTFVEELVLKALFFSGEMRGMDIAARLQLPTALVDDVIEGLRRQKYIDIRGGGGSGVGKSTMIYQLTTFVTDMLRQVLDRNRYNGPAPVPFLEWAAAVKRQTVRGNRITRARMQDKFGDLIIKDYIFDGIGPAMNSGRAIFFYGPPGNGKTAICQGMVNCFDGDIFIPHAILIDDFVVRIFDANLHKAVEDEPGMQPYDRRWVRCRRPLVVVGGELTLEMLDLVYSPEVKYYEAPFQMKASNGMLLIDDFGRQKVSPKDLLNRWIVPLESDIDMLTLHTGKKLQVPFDVFAAFSTNLDPSDLVDDAFLRRVRYKLEVQRPDEEQFHDIFQVMCRKRGVPYNAAAVDYLIDAHYRPVGRPFAACQPRDLLDQVIDMAHYQGQEPRLTTELLDSAVRGYFVRFDKDKPEATSASAG
>NZ_CP022203.1|WP_095959184.1|4808034_4808949_+|hypothetical-protein
MTSTQARNAARPWLLLLPLPAMLLGAFTAWRSGAPAGAFILNAAAAALGAGVAVLLGRQPGLTLPRAATPLAVIAILVTASTLLFPGLEGIHRWVALGPVRLHASAIATPWVLLGMSAALHQRLAVSAALALSMAAVHAAQPDAGQGTAFALAASVLLARAQLAPWPARAATCAGVLAMGAMAWLRPDPLAAVPHVERIVQLAAGLTPVLGAVAVLALALLLVPTVPGITVGRDLSLGLAVYLAATLCVPALGNFPVPVMGAGAGPVLGWYLATGMLMAAARRPPGSSPPRRAPRPPRGGTLEA
>NZ_CP022203.1|WP_095959185.1|4808945_4810607_+|acyl-CoA-dehydrogenase-family-protein
MSFFQDPPRLGNQYDDDSLLQSYLARTLPDDLRRGLTDEFLELGDLGGDYFYRFQLRDRLNEPELTQWDAWGHRVDHIEVSPLWKEAEALAARRGLVATAYEQKSAELSRVHQFVLNYLVQPSLDVYSCPLAMTDGAARSLLTLGNQALIDRALPHLTSRNPATAWTSGQWMTERTGGSDVGLTQTVARQTPEGWRLSGTKWFTSATTAQMALTLARPEGNGPGGKGLALFYVETRDAAGKLNGIQINRLKDKLGTRKVPTAELTLDGTLAVPVAGLTDGIRNMAWMLNVTRTWNAVGSAWSMRRALALARDYAQRRVQFGARLADKPLHVDTLAGLEAEFQAGFLLAFRAVELLGRMEAKVATEQELLLQRLVTPLAKLTTGRQVVHVTSEVTESFGGAGYVEDTGIPRLQADAQVLSIWEGTTNVLSLDALRALAKEGTLEALFSEVETRLGQVRDAGLRPCVGAAHAALEHARAWVSGALESPTTLEAGARRFALTLGRTLELALLSAHAQWCLDQGHGPRSRAAARRFASHGVNLIQQEASLEDARLLA
>NZ_CP022203.1|WP_095959186.1|4810931_4811687_+|hypothetical-protein
MPAMQTMRWRSLGEMIGDLELPESCYAEQLSRDDIPRVTKLLGTWYPDIRVGTESRHLEPSFYDKEVYLRGESPDRPVYAMLGRDRATGDIIGLLTLERNVRGLQVSATMGVLEPSQRGLGLGQVGLSVLEQVGRSIGAEVILYYSTLKLARVQRNAEHRGFTLVGLVPAFDVDAIAPNTVKRVYEAIYAKVLVGPEQIHLPDWNALTPTTRALYTHLFGQHPSAAAAEGATPAFSVPASAQRPAPEVRHG
>NZ_CP022203.1|WP_095959187.1|4811679_4812729_+|GNAT-family-N-acetyltransferase
MVEVRSFEGDAKEASQFLNGIWQRTYGAKMALTVWDERFFDWLLFSNPLVDRDYMLGAYSKGKLVGAFFAEPAKIQLGQRQVDGTYGSWATVAPEHRRQGIGVKLSDAMLSRHRERGAALTLACVADGTLGQAFWGQRSHARHLNGLGLWLHVFDRQKVVRWSLSATERAFLTLTRPFQRHRFQEASTEGIRAYEPRDLPQCMALVQQMMRPVNLGYAYTTERLAHQLQYRQTPRTFVLEREGVIQGLVNSYMLQMTARGLLSVGLVDMLAFQAALPLSEQRRLLWVAMQDMVAQGAECAAMLRSPCTPPSLMLRSGWLPFPGGSRVTCLLTTPDVELPASPRVFMHLR

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Crispr_ID: NZ_CP022203_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_9

5086268-5086488

Orphan

Consensus_repeat	Method
GCACCAGCCTCACCCGCGGCACC	CRT

4 spacers

The CRISPR arrays of NZ_CP022203_9

>merge|NZ_CP022203|9|5086268-5086488|CRT
GCACCAGCCTCACCCGCGGCACCAGCCTCACCCGGAGCCGCTGCGGCACCGGCCTCACCCGGAGCCGTCGCGGCACCGGCCTCACCGGCAGCACCAGCCTCACCCGCGGCACCGGCCTCACCCGGAGCCGCTGCGGCACCAGCCTCACCCGCGGCACCGGCCTCACCCGGAGCCACTGCGGCGCCAGCCTCACCGGCGGCGCCAGCCTCACCTGCGGCACC

>NZ_CP022203|9|3|5086268-5086488|CRT
GCACCAGCCTCACCCGCGGCACC	AGCCTCACCCGGAGCCGCTGCG
GCACCGGCCTCACCCGGAGCCGT	CGCGGCACCGGCCTCACCGGCA
GCACCAGCCTCACCCGCGGCACC	GGCCTCACCCGGAGCCGCTGCG
GCACCAGCCTCACCCGCGGCACC	GGCCTCACCCGGAGCCACTGCGGCGCCAGCCTCACCGGCG
GCGCCAGCCTCACCTGCGGCACC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_170114751.1\|5088305_5090510_+\|PQQ-binding-like-beta-propeller-repeat-protein	unknown	unknown	gnl\|CDD\|379140
NZ_CP022203.1\|WP_095959303.1\|5084418_5085333_-\|HEAT-repeat-domain-containing-protein	unknown	unknown	gnl\|CDD\|379311
NZ_CP022203.1\|WP_013940755.1\|5076010_5077135_+\|alanine-dehydrogenase	unknown	unknown	gnl\|CDD\|240630
NZ_CP022203.1\|WP_095959306.1\|5090523_5091516_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959311.1\|5097135_5097828_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP022203.1\|WP_095959302.1\|5083805_5084441_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959297.1\|5074529_5075834_-\|radical-SAM-protein	unknown	unknown	gnl\|CDD\|100105
NZ_CP022203.1\|WP_095959313.1\|5099424_5100603_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959298.1\|5079117_5080809_+\|response-regulator	unknown	unknown	gnl\|CDD\|224117
NZ_CP022203.1\|WP_095959300.1\|5081983_5082754_-\|type-III-pantothenate-kinase	unknown	unknown	gnl\|CDD\|237349
NZ_CP022203.1\|WP_013940756.1\|5077377_5078019_+\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|236608
NZ_CP022203.1\|WP_095959308.1\|5093228_5094920_-\|DUF692-family-protein	unknown	unknown	gnl\|CDD\|377459
NZ_CP022203.1\|WP_095959312.1\|5097796_5099437_+\|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_CP022203.1\|WP_043711467.1\|5078041_5078941_+\|anti-sigma-factor	unknown	unknown	gnl\|CDD\|227949
NZ_CP022203.1\|WP_095959309.1\|5095000_5095816_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379326
NZ_CP022203.1\|WP_095959310.1\|5095952_5096828_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959301.1\|5082767_5083772_-\|biotin--[acetyl-CoA-carboxylase]-ligase	unknown	unknown	gnl\|CDD\|237010
NZ_CP022203.1\|WP_095959307.1\|5091492_5092524_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|224932
NZ_CP022203.1\|WP_095959299.1\|5080853_5081987_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_043711474.1\|5092524_5093160_-\|uridine-kinase	unknown	unknown	gnl\|CDD\|235492

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_170114751.1\|5088305_5090510_+\|PQQ-binding-like-beta-propeller-repeat-protein	gnl\|CDD\|379140	pfam13360, PQQ_2, PQQ-like domain. This domain contains several repeats of the PQQ repeat.	5.69649e-13
NZ_CP022203.1\|WP_095959303.1\|5084418_5085333_-\|HEAT-repeat-domain-containing-protein	gnl\|CDD\|379311	pfam13646, HEAT_2, HEAT repeats. This family includes multiple HEAT repeats.	6.86836e-09
NZ_CP022203.1\|WP_013940755.1\|5076010_5077135_+\|alanine-dehydrogenase	gnl\|CDD\|240630	cd05305, L-AlaDH, Alanine dehydrogenase NAD-binding and catalytic domains. Alanine dehydrogenase (L-AlaDH) catalyzes the NAD-dependent conversion of pyruvate to L-alanine via reductive amination. Like formate dehydrogenase and related enzymes, L-AlaDH is comprised of 2 domains connected by a long alpha helical stretch, each resembling a Rossmann fold NAD-binding domain. The NAD-binding domain is inserted within the linear sequence of the more divergent catalytic domain. Ligand binding and active site residues are found in the cleft between the subdomains. L-AlaDH is typically hexameric and is critical in carbon and nitrogen metabolism in micro-organisms.	0
NZ_CP022203.1\|WP_095959311.1\|5097135_5097828_+\|response-regulator-transcription-factor	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	2.24043e-77
NZ_CP022203.1\|WP_095959297.1\|5074529_5075834_-\|radical-SAM-protein	gnl\|CDD\|100105	cd01335, Radical_SAM, Radical SAM superfamily. Enzymes of this family generate radicals by combining a 4Fe-4S cluster and S-adenosylmethionine (SAM) in close proximity. They are characterized by a conserved CxxxCxxC motif, which coordinates the conserved iron-sulfur cluster. Mechanistically, they share the transfer of a single electron from the iron-sulfur cluster to SAM, which leads to its reductive cleavage to methionine and a 5'-deoxyadenosyl radical, which, in turn, abstracts a hydrogen from the appropriately positioned carbon atom. Depending on the enzyme, SAM is consumed during this process or it is restored and reused. Radical SAM enzymes catalyze steps in metabolism, DNA repair, the biosynthesis of vitamins and coenzymes, and the biosynthesis of many antibiotics. Examples are biotin synthase (BioB), lipoyl synthase (LipA), pyruvate formate-lyase (PFL), coproporphyrinogen oxidase (HemN), lysine 2,3-aminomutase (LAM), anaerobic ribonucleotide reductase (ARR), and MoaA, an enzyme of the biosynthesis of molybdopterin.	1.04881e-13
NZ_CP022203.1\|WP_095959301.1\|5082767_5083772_-\|biotin--[acetyl-CoA-carboxylase]-ligase	gnl\|CDD\|237010	PRK11886, PRK11886, bifunctional biotin--[acetyl-CoA-carboxylase] ligase/biotin operon repressor BirA.	5.95734e-86
NZ_CP022203.1\|WP_095959300.1\|5081983_5082754_-\|type-III-pantothenate-kinase	gnl\|CDD\|237349	PRK13321, PRK13321, type III pantothenate kinase.	1.14309e-163
NZ_CP022203.1\|WP_013940756.1\|5077377_5078019_+\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|236608	PRK09652, PRK09652, RNA polymerase sigma factor RpoE; Provisional.	1.39965e-58
NZ_CP022203.1\|WP_095959308.1\|5093228_5094920_-\|DUF692-family-protein	gnl\|CDD\|377459	pfam05114, DUF692, Protein of unknown function (DUF692). This family consists of several uncharacterized bacterial proteins.	3.18868e-22
NZ_CP022203.1\|WP_095959312.1\|5097796_5099437_+\|HAMP-domain-containing-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	7.39658e-40
NZ_CP022203.1\|WP_043711467.1\|5078041_5078941_+\|anti-sigma-factor	gnl\|CDD\|227949	COG5662, COG5662, Predicted transmembrane transcriptional regulator (anti-sigma factor) [Transcription].	1.71826e-14
NZ_CP022203.1\|WP_095959298.1\|5079117_5080809_+\|response-regulator	gnl\|CDD\|224117	COG1196, Smc, Chromosome segregation ATPases [Cell division and chromosome partitioning].	1.87867e-18
NZ_CP022203.1\|WP_095959307.1\|5091492_5092524_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|224932	COG2021, MET2, Homoserine acetyltransferase [Amino acid transport and metabolism].	2.28045e-46
NZ_CP022203.1\|WP_095959309.1\|5095000_5095816_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379326	pfam13673, Acetyltransf_10, Acetyltransferase (GNAT) domain. This family contains proteins with N-acetyltransferase functions such as Elp3-related proteins.	3.50652e-10
NZ_CP022203.1\|WP_043711474.1\|5092524_5093160_-\|uridine-kinase	gnl\|CDD\|235492	PRK05480, PRK05480, uridine/cytidine kinase; Provisional.	8.97514e-109

>NZ_CP022203.1|WP_095959303.1|5084418_5085333_-|HEAT-repeat-domain-containing-protein
MKPVLLLASCVVLLGACRWRAPRYPVAPVELTGVTLQDNALLGLAPEGVATLFTVALKDSGRFEQKGEDAPREERPWRLTLDVPFTREVLKDGDPRSFAEVGANLVLERFGGRLPQRYELVGLGEAPVEEDSPAGRQKAMRTALANVLRQVTESAIMQLTALDRTDDELVLDLKATDARVREFSLRTLAERQHPAAAPLLIDRLKEATDAETVRRTMGALVEMKARVAVPVLIDLARGRDLGFVQEIVFAVGEIGGPEAEAYLYTMAQGHDAPAVQAAAQQALDTLYASRKHSPAEARGPGRAD
>NZ_CP022203.1|WP_095959302.1|5083805_5084441_-|hypothetical-protein
MAQAARTDIEMKRSFGVGGAVVLGALMLGTGCSKNVEAAADSGASTGDVAEYYPLAVGNRWTYRLNGREDKEVTVEILKEEAGVFHDNQGGQLFLDGYGLRDPKRYLLRGPLKEGHSWTNVVSVSSTERYRIVQAGESCQTLAGTFPRCVQVEARNRMDAKATMVNTMTFAPGVGMVRIETVVEANGQLVPQTLLELTAWQLRDGAAPPSG
>NZ_CP022203.1|WP_095959301.1|5082767_5083772_-|biotin--[acetyl-CoA-carboxylase]-ligase
MPVQVNEQSQEALILSFLSESGSDYTSGEALSSKLGLSRTAVWKHVESLRAKGYRIEAVPARGYRLVEVPDRLTSLEIGPLLDTHDLGRTVHHHESLPSTNERAFRLAQDGAGHGEVVVAEQQTAGKGRRGRTWVSPSGLNLYFSAILRPELPPQRAPELTLVAAVALAEALRDAGADAAIKWPNDVHIDGRKVAGILTELSAEPERVHFVVVGVGVNLNALAEHFPEELRATATSLALALGHPVKRAPFTAALWTRLEEWLDLYLETGFDAVRARWKALSSTLGQDVLVRTDRQALRGHAEDIDPSGALLVRTEGGSLERVLAGDVEQLRPRR
>NZ_CP022203.1|WP_095959300.1|5081983_5082754_-|type-III-pantothenate-kinase
MLLAIDVGNTNTALGVFEGRRLLDHWRMETSTRRTSDEYGILVRQLFTHRGIDPAKVTAVAVSSVVPPLQSNLEKMSERYFKLRPMFVGPGVKTGMPIFYDNPREVGADRIVNAVAAYEKHHAGVLVVDFGTATTFDAVSPKGEYLGGCICPGINISMEALFQNASKLPRVEFARPPHVIGRNTVHSMQAGLVYGFVGLVDGICARMQAELGFPVKVVATGGLASLVASESKAIHQVDEFLTLEGLRIIYGRNHAS
>NZ_CP022203.1|WP_095959299.1|5080853_5081987_-|hypothetical-protein
MTTAAPNNVPAPPPGCPFDAEFLPPNMRKHVDPAAPVPLRMMAAKTLVPLNPSDMLGALYMLTFDPDAGVRETVAKTAAMLPDKILGSALRDEEVQPQVLGYFLGLVKDKEAYAEMLVLNASTPDDAVADVAKDCGPKLAEIIGQNQLRLLRHEDILRNLCANASAPVSLIDNVCDFAVRSGMQLLDVPQMKAARVRVFGPEAAETPPPQGPTAEEVLQEFQEAADESAAPMEEGKRLTLAQRIMRMSIAEKIKLATLGNKEARTALIRETNKLVAVAVIRSPRITDGEVLACAANRAMMDDVLRVIYSNREWTKNHKVKMALVKNPKVPLTVTMKFLNAFRDAELKDLSRDKNVPAAVQGFAKKLHEKKTTPKKQG
>NZ_CP022203.1|WP_095959298.1|5079117_5080809_+|response-regulator
MSKKILIVESDTALSASLRSALEGRGFTVDETTDGKGSVEQIRRDRPDLVVLAVDLSAGQNGYLICGKLKKDDDLKNVPIVIIGNPDGFAQHRKLKAHADEYVAKPVDADLLVDRVGALIGFPELPAAALEDVVDESLTLDALGDEPMTADFGEEISVETAEEPPVTGEELDLDAAFGDLSAPEETPAFEEEVVVAPPEAVVEGVEEDFSTLDSLGTDAEDALDGLDDSEKTVVGFLAPAPTPAAPPPEPPRAVAPPPAPRAVAPPRPAPPPVSVAPAADAVELRGLRAKVAELQAELDDSRGTASHAEERVRDLEVQLEAQATELEAARASSGKNDKDTFALRDAANKKDKEILRLKTELNQKDQEIIELKDQNLELEQKASTAESELTQRDAQLKTLSARADSLAADRKRVDQQLSAAKDEARSASAQLTALQAELDQHQAQAHAYAAELEDLRARAGQLEADVQAARSEAEDLRVQLGQAQVELSEQSSRANAEAEELRGRIAELEAATARSEERVTRLYARIKSEEKLREKTKKALVIAQQLLEEPASAVADDASEAAA
>NZ_CP022203.1|WP_043711467.1|5078041_5078941_+|anti-sigma-factor
MNCQDLERLLYPYLDGEFQPEERVDLETHLSGCAACRRRAEEEKQMQQALRRAARHSVSGMRAPASLRAGIQVGLKQEQRRAQVGVWLRAGAMALVVVTVGGGWAAFHTEQRLSAARTEAVQRHSKSKALPFEIASNTPEQVEEWFKDKVDPRITVPQLPKAKPLGGRISILNGREVAYISYETLPDNEDEPRRRLGVFVLPGDDEGALPKFQALQAVEVDSAQGFNVVTWRDDEIVYEMVTDMDESDIRRMLAERDSGEKLARKSAPESDEPLYSLPPAVRPPYSRPPISIEPVTYPQ
>NZ_CP022203.1|WP_013940756.1|5077377_5078019_+|sigma-70-family-RNA-polymerase-sigma-factor
MLDFRQPNRTKQEFEELALAHLDPLYSAALRLTKNERDAEDLVQDTCMRAYRFFDKFERGTNIKAWLFKILTNTFINRYRRKVKERTVVEGVEREAVHERFVSRDATDFAANPEQYFFDRLLSDDVLRAIDSLPIDFRLVVILADLQEFSYKEIAEILECPVGTVMSRLFRGRKLLQKNLREYAEGQGVFRHDGEPVNAPADLEEYRHRKKTG
>NZ_CP022203.1|WP_013940755.1|5076010_5077135_+|alanine-dehydrogenase
MIVGVPKEIKTREYRVGMVPAGVSAFIAAGHTVLIETNAGVGSGIPDSEFQRVGAQIVASADELWKRSEMIIKVKEPIAPEYARIQPGQIIYTYFHLAGVDPELTRTLIQKKAAAVAYETLQLDDGSLPLLKPMSEVAGKMAIQVGAKCLEKAHGGKGILLGGVPGVRRGRVTVIGGGVVGLCAAKVALGMGAEVTILDVNMERLTYLDDVFLGRVGVLASDSESIARSVREADLVVGAVLIPGGKAPKLVSEALISEMTPGAVVVDVAVDQGGCIETCKPTTHDNPTFEVHGVVHYCVANMPGAVPQTSTYALTNVTRPHSRKIADMGLIEAVKSDRALARALNTYNGHVTYEAVAKDMGYPYMPINDALAGK
>NZ_CP022203.1|WP_095959297.1|5074529_5075834_-|radical-SAM-protein
MTSAPKLLFADPKGRVMEHPYLLATLRSGEELVPPQDKPIPLPSAGRLVHLPGRLPVGLHPETGELELVREMKVGGKTFVPNAVGALLPPGYTRTFLPGEVKGSGPVLPQWAYTAAAWVGDGPVAWAIHTDRRSHWNPERFSTPEMKGLVAQHLARFPDNRVLKQLKTCALVYSCFTSQNTFYVRDEAAIPASVMCNARCVGCISDQPADGPPASHERMDDGPTGEEMGQIGLFHLEHAPGRTMVSFGQGCEGEPLTRWKQIAEAIRYMRARTQAGSININTNASLTRGLEALFDAGLDAIRVSLNSAVKDLYEAYYKPVKYGWEDVEASIALARERGAYLALNLLLFPGVTDREGEVRALERLVKKYRVDQVQTRSLCIDPLQYLEVARERGAGGEPVGIRTLLQRLKAARPGLVVGNFARGLEERENAAGPR
>NZ_CP022203.1|WP_170114751.1|5088305_5090510_+|PQQ-binding-like-beta-propeller-repeat-protein
MTRIRIGQRWKREPAASPLDSIALELDGVDLLSGAVEESLAEVVPSLVRSVAALAGGRQKLAQVSLPEAHLELVLRRVGPEVELLVANLSRPARLMRPPVRVELEELVEAVREAGERFLADVTRAGPKALATPLGQALKEPLKSLKRPARPPDEVPARPATRRLEPAEVPGFGFELRDAGLPTGAGRGAARGTAGLLAPLLAGGEVWLSLPGRPDAWRVPGPPFLTVLELSRLAVELARAVELGERRFELAPAGAKPPLLLDLKTGQARAGRTGAPFPLPGSVLAAALFHLGESLAAAFAEADRALVGNPYRAELAERCREGLSHLRGPVQPPEAQGAAREKKARAKGQGTSRPLKVPGRLRRLRFEKLWEKRGLPDAEEARLLLGRHGPVYCAPQLTSAFSRKDGALLWKRAAALGVAASADGHAVAADIARVYGFTGRGSGARWLHDHDGIPLGPLLLRKDGLLLTLSEDRTVVAFAEATGREVWRLAPPRTQRSWLATQGHRALVGTDSGYLYGLDLEDGQVRYRMRAPMPFHGAPVAWGKRFLAMLGRGSHWALLLADAHTGEAVWTYEPDLSHLSAPLPVGSRVFIAGEREREGVLLCLDAKGRRLWERPLNLGPGPYALAPLPRAVVVTSASGAATRVAASGTVDWRVGAAGEPLIGALPAHTARDVTLVPGERVRAVDPRGGQVLAEVQAGVGLVALQADVRLNLYFLDDAGTLSAYRLGSHFTVVE
>NZ_CP022203.1|WP_095959306.1|5090523_5091516_-|hypothetical-protein
MGPGGLDHVGEFSYHCQDKGTGDCRVKRYFGVIVIVAGVLLGAVMSYRSASGRALEAQREADQQRIHAEYLERVGWMRSNPDEASYRDELKPFFKNYFEQVDDHLTRFQGNTKFDDYLLELEQREERGAKDDRANDRKAFYEYARKTFDSMREGRYRPVWTATDKGMRLDLISSDVVMVLGKPQIRLQLAVWGAQRTLKDDGKVLKMVTSAAFDTVWKLTDAKGKLLGEMRGADPSMKIDHPERFIKAFPPQMVLGHYDLDLLPNEVSKMEMTINLTSSAASGGTATSTYVWKVDEVPSDWKLGAGESWEGATQEERPEEEIDPSKAARD
>NZ_CP022203.1|WP_095959307.1|5091492_5092524_+|alpha/beta-fold-hydrolase
MIQATGTHLFTTPLPLEEGELLGNPQVAWAAYGEPSDGKAVVLLHDLAHSHLALGPPEDSAYQPSGWGRALVGTNLALDPAVTPVLAPGLLGSPFGSTSPATVNPASGERWGLELPPLTVQDMARAVSATLRACGLSHVRALVGVGLGGHVALRLASLFPDLADGVVTLGAARALPEAVREKLGLSWQVLRADPDYRDGLYALDAPPRKTMRKLRLDFQKLLAGREHLTATYRDAESARAALDAEADAFADAFDAVSWASLCSAYAGSDVSDGFARIRSRVLLIAGASDAMAPVNRVRDTYHLLSAAGVSARFLELPGPGDHAALLQDSERLHGPLSDFLRRC
>NZ_CP022203.1|WP_043711474.1|5092524_5093160_-|uridine-kinase
MASPLVVGIAGGTASGKTTVARKVREALADCRVAFIDQDSYYRDLKDLPLADRREVNFDHPDAFDRELLVKHLKALKSGQPIQKPVYDFVTSSRQPQTKNVEPGDIILIEGILVLHMKEVRDEMDVKIYVDADDDLRILRRLTRDIKDRGRDFDHVVSQYLRHVRPMHMGFVEPSKHFADIIIPHGGNNEIAIGMLVGALRGKLSGVAQRD
>NZ_CP022203.1|WP_095959308.1|5093228_5094920_-|DUF692-family-protein
MAVAAGRVYVEEMTHAAPPSWTLPWRGLGLSSNLSMADVPQPYRLLDASPGLFDYVEYSAPLSLEESKAHASLFPEMWRRRQDVPVLFHPVHLNLWGPGLEPARALVELDAHARAVESPWVGNDVGWWHVEGQPFPGYLYFTPPFNEAGLEASVAHALHVQRHLSMPLVLENPAVLARRGQWHVLDFMAKLHARTGAPLLLDLGHLFSHQLSAGLPLETGLEGFPLDQVIELHIAGGVVTHRGPRRFYVDDHTQPVREELFELLASLIPRCPSLRAVTFEGDGHPPEVAAASLRRLRELVPAGARPPLTWRVPEASAAPVPALTEDSQPWALFDAGYGAAPVTSVEDEAGTLADQDFRLAVVAEVLDRDWPLTRLLLAGTREALAAFTGSKEFRKLFSPLGRSPGQAFASWAMRRLRESPDEGGSAALTLEMLLPSLFLRRVPAPAPGQVGLMEDVRAGSLPVDLSELVHAARAVRRHLTARAWASGVLELSGLESLNQVARRAGPGPWSFTARRRAGGLEVTTVSPAMGEFLRMLAVQPLTEAEVAPGLVEEARQRGLIRRG
>NZ_CP022203.1|WP_095959309.1|5095000_5095816_+|GNAT-family-N-acetyltransferase
MPPASRAEIDESNAQYRGAWRLFALGSKAGEVVERPDVYITACNVAWSMMNAAFLRAPVETEQALAAAAASAARYFSAGKHGWSFLICDDWLAPAVRDNAPSILDWYGLKPELVVTGMVADRLQPSLHPPSPFDLRPVTDAGGRQAVADINALSYDVPQHLGREAFDEATLYNADCQGFVACRDEEPAASTVVLRVDAAAYVALVATHPQHRRQGAAEAVMRHALARARQDWGTERTVLHATEAGQPVYTRLGYRPVTRFRMYLAPPPGQG
>NZ_CP022203.1|WP_095959310.1|5095952_5096828_+|hypothetical-protein
MPHVLHRPATRSPHMAKWDDLVLAIPPHAGGRLEVPAPAALLETLLGLHNVQLTLLRGLRRELRPLQEGPFHAGRTHLEAARVAHASRDEQLERLKAARGCFTEAMGMERDKARLSFIALHLGLCWLLLGAERDAREWTQLAHRTAVEAMKDILVDASKHQGLTRNRYLAPAITFFMFFTSAATLGAGYLFWDRVLSKRTGTVMRRALVQMQSLADYVDALGEIRLRLGELSHDVARYELTHGVDEQQFVARITIRKLINDREAIYFNGRETRKVTWNDQERSEVITRELL
>NZ_CP022203.1|WP_095959311.1|5097135_5097828_+|response-regulator-transcription-factor
MAERPTVLVVDDDPHLREIVRFALEQGGFRVDEATDGRAALAQVDRALPALIVLDIMMPELDGLAVCREVRRKHELPIVFLSSRDDEVDRILGLELGGDDYLTKPFSPRELVARVKAVLRRARPAPEAEAPPARMQSRGPLRMDAERWRAWWRDTEVVLTVTEFQLLATLLRVPGKVFTRDELMNRVYDDVVVSDRTIDSHVRRVRQKFASAGGDVIETVHGLGYRLALP
>NZ_CP022203.1|WP_095959312.1|5097796_5099437_+|HAMP-domain-containing-histidine-kinase
MALAIGSPSPERRARPRLWLVFAAVGVAGFALTLAGLAFVRVYDNQLIRQTESELIAQGAVIAEVFRERLRDAEPRDDHGRERTAPWPFPLPDDTRLRPILPSLRASDATLPSGGTPQPSRVPAEPLAHAAGLRLTPLLEQVRAATLAGIRVVDPEGVVVASSSASLLGTTLADRTEVQRALRGEPVSVLRRRVAEPEDTPLASLSRDTGIRVSVALPVLDGERVWGAVVLTRTPMTFAKATYADRWNLTATGFVLLGVVALMSLAAAALVGRPVRALMRQTRAIALSDPSGFEPVARPVVAELAELSESLAGMATALRDRNQYIRSFAANVSHEFKTPLASIQGAVELLRDSADAMSPEQRARFLANVDADARRLTRLVQRLLELARADSMTATPAQVALGPLLEGLALRARAEGALDIHVTPPPAGLTMGLPQEVLDDVLWQLVTNARQHGGDTVRVDLSVEQAPEADLVRVVVKDSGRGISEANRARIFDAFFTTARARGGTGLGLTIAQSMLRAFNARLELLPSATGTTFAVVAPVRGLQRK
>NZ_CP022203.1|WP_095959313.1|5099424_5100603_-|hypothetical-protein
MWTVPLFVGLLLTTADAAAASTPSGTATVPLQELIPLYAQRQDAPATPPPTDALVKSQLKGRLTADALFVDGHFDVEVLADGRWTQVRLLQLDADTYPATLPSLEGGTVGVVDGYLCLLTRKAGRYVFDVGVSIRSPGTGPERRARLRFGPHAPPVPLALEADTSVFTLTEPLASLGGESHAVYPVQGALRVGWRASVARAASSQKQQVRPPLEPRITEATASWVSTLEGRATLRVSYALSLDREQPLELVLPEGHRLERVTLNAIPVPVESQEGTLTLKAAPARLGETGGTLEVVLSRELGVFHLSGRLKLALPRVSWPVAELRAKAHFPAVFNYRREGGSLEQYESPESATPETSGLPGKALHFRQFLVAASAPTLELGYSVDISDSYFR

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Crispr_ID: NZ_CP022203_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_10

5157132-5157274

Orphan

Consensus_repeat	Method
CGGACGGAACGTTCATTCCGGGC	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP022203_10

>merge|NZ_CP022203|10|5157132-5157274|CRISPRCasFinder
CGGACGGAACGTCCGTTCCGGGCACTGCGACGACGCTGGACTCCGGCTGAGGCCTGGCGCCGGACGGAACGTTCATTCCGGGCGCCCATGCAGAGACGGACGCCACCGGCGCCATGGCTGCGGACGGAACGTTCATTCCGGAC

>NZ_CP022203|10|7|5157132-5157274|CRISPRCasFinder
CGGACGGAACGTCCGTTCCGGGC	ACTGCGACGACGCTGGACTCCGGCTGAGGCCTGGCGC
CGGACGGAACGTTCATTCCGGGC	GCCCATGCAGAGACGGACGCCACCGGCGCCATGGCTG
CGGACGGAACGTTCATTCCGGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_013940824.1\|5159296_5160226_-\|lipoyl-synthase	unknown	unknown	gnl\|CDD\|235493
NZ_CP022203.1\|WP_095959342.1\|5152064_5153297_+\|molybdopterin-molybdotransferase-MoeA	unknown	unknown	gnl\|CDD\|238452
NZ_CP022203.1\|WP_095959347.1\|5160484_5161882_-\|dihydrolipoyl-dehydrogenase	unknown	unknown	gnl\|CDD\|235798
NZ_CP022203.1\|WP_095959341.1\|5150477_5151869_-\|protease-inhibitor-I42-family-protein	unknown	unknown	gnl\|CDD\|378179
NZ_CP022203.1\|WP_095959338.1\|5145070_5145814_+\|DUF2807-domain-containing-protein	unknown	unknown	gnl\|CDD\|371327
NZ_CP022203.1\|WP_095959343.1\|5154150_5154972_+\|MBL-fold-metallo-hydrolase	unknown	unknown	gnl\|CDD\|293801
NZ_CP022203.1\|WP_095959348.1\|5161899_5163087_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959336.1\|5142702_5143917_+\|metallophosphoesterase	unknown	unknown	gnl\|CDD\|277331
NZ_CP022203.1\|WP_095959351.1\|5165961_5166498_-\|imidazoleglycerol-phosphate-dehydratase	unknown	unknown	gnl\|CDD\|153419
NZ_CP022203.1\|WP_013940830.1\|5165200_5165962_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	unknown	unknown	gnl\|CDD\|234996
NZ_CP022203.1\|WP_095959340.1\|5146109_5150369_-\|ribonuclease-R	unknown	unknown	gnl\|CDD\|273947
NZ_CP022203.1\|WP_095959352.1\|5166494_5167211_-\|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase	unknown	unknown	gnl\|CDD\|240083
NZ_CP022203.1\|WP_095959337.1\|5144065_5144854_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|276809
NZ_CP022203.1\|WP_095959349.1\|5163816_5164425_-\|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE	unknown	unknown	gnl\|CDD\|235067
NZ_CP022203.1\|WP_095959344.1\|5154961_5156053_-\|lipoyl(octanoyl)-transferase-LipB	unknown	unknown	gnl\|CDD\|319743
NZ_CP022203.1\|WP_095959339.1\|5145842_5146061_-\|DUF3185-family-protein	unknown	unknown	gnl\|CDD\|378652
NZ_CP022203.1\|WP_095959350.1\|5164424_5165204_-\|histidinol-phosphatase	unknown	unknown	gnl\|CDD\|273949
NZ_CP022203.1\|WP_013940819.1\|5153414_5154089_+\|GTP-cyclohydrolase-II	unknown	unknown	gnl\|CDD\|234745
NZ_CP022203.1\|WP_013940827.1\|5163101_5163551_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095959346.1\|5157970_5159236_-\|2-oxo-acid-dehydrogenase-subunit-E2	unknown	unknown	gnl\|CDD\|237001

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_013940824.1\|5159296_5160226_-\|lipoyl-synthase	gnl\|CDD\|235493	PRK05481, PRK05481, lipoyl synthase; Provisional.	8.37079e-176
NZ_CP022203.1\|WP_095959342.1\|5152064_5153297_+\|molybdopterin-molybdotransferase-MoeA	gnl\|CDD\|238452	cd00887, MoeA, MoeA family. Members of this family are involved in biosynthesis of the molybdenum cofactor (MoCF), an essential cofactor of a diverse group of redox enzymes. MoCF biosynthesis is an evolutionarily conserved pathway present in eubacteria, archaea and eukaryotes. MoCF contains a tricyclic pyranopterin, termed molybdopterin (MPT). MoeA, together with MoaB, is responsible for the metal incorporation into MPT, the third step in MoCF biosynthesis. The plant homolog Cnx1 is a MoeA-MogA fusion protein. The mammalian homolog gephyrin is a MogA-MoeA fusion protein, that plays a critical role in postsynaptic anchoring of inhibitory glycine receptors and major GABAa receptor subtypes.	2.95797e-167
NZ_CP022203.1\|WP_095959347.1\|5160484_5161882_-\|dihydrolipoyl-dehydrogenase	gnl\|CDD\|235798	PRK06416, PRK06416, dihydrolipoamide dehydrogenase; Reviewed.	0
NZ_CP022203.1\|WP_095959341.1\|5150477_5151869_-\|protease-inhibitor-I42-family-protein	gnl\|CDD\|378179	pfam09394, Inhibitor_I42, Chagasin family peptidase inhibitor I42. Chagasin is a cysteine peptidase inhibitor which forms a beta barrel structure.	5.30737e-13
NZ_CP022203.1\|WP_095959338.1\|5145070_5145814_+\|DUF2807-domain-containing-protein	gnl\|CDD\|371327	pfam10988, DUF2807, Putative auto-transporter adhesin, head GIN domain. This bacterial family of proteins shows structural similarity to other pectin lyase families. Although structures from this family align with acetyl-transferases, there is no conservation of catalytic residues found. It is likely that the function is one of cell-adhesion. In Structure 3jx8, it is interesting to note that the sequence of contains several well defined sequence repeats, centred around GSG motifs defining the tight beta turn between the two sheets of the super-helix; there are 8 such repeats in the C-terminal half of the protein, which could be grouped into 4 repeats of two. It seems likely that this family belongs to the superfamily of trimeric auto-transporter adhesins (TAAs), which are important virulence factors in Gram-negative pathogens. In the case of Parabacteroides distasonis, which is a component of the normal distal human gut microbiota, TAA-like complexes probably modulate adherence to the host (information derived from TOPSAN).	2.91273e-32
NZ_CP022203.1\|WP_095959343.1\|5154150_5154972_+\|MBL-fold-metallo-hydrolase	gnl\|CDD\|293801	cd07715, TaR3-like_MBL-fold, MBL-fold metallo-hydrolase domain of Myxococcus xanthus TaR3 and related proteins; MBL-fold metallo-hydrolase domain. Myxococcus xanthus Tar3 may function as an ammonium regulator/effector protein involved in biosynthesis of the antibiotic TA. Some are members of this subgroup are annotated as ribonucleases. Members of this subgroup belong to the MBL-fold metallo-hydrolase superfamily which is comprised mainly of hydrolytic enzymes which carry out a variety of biological functions.	1.85631e-115
NZ_CP022203.1\|WP_095959352.1\|5166494_5167211_-\|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase	gnl\|CDD\|240083	cd04732, HisA, HisA. Phosphoribosylformimino-5-aminoimidazole carboxamide ribonucleotide (ProFAR) isomerase catalyzes the fourth step in histidine biosynthesis, an isomerisation of the aminoaldose moiety of ProFAR to the aminoketose of PRFAR (N-(5'-phospho-D-1'-ribulosylformimino)-5-amino-1-(5''-phospho-ribosyl)-4-imidazolecarboxamide). In bacteria and archaea, ProFAR isomerase is encoded by the HisA gene.	8.47742e-82
NZ_CP022203.1\|WP_095959336.1\|5142702_5143917_+\|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.	2.85352e-80
NZ_CP022203.1\|WP_095959351.1\|5165961_5166498_-\|imidazoleglycerol-phosphate-dehydratase	gnl\|CDD\|153419	cd07914, IGPD, Imidazoleglycerol-phosphate dehydratase. Imidazoleglycerol-phosphate dehydratase (IGPD; EC 4.2.1.19) catalyzes the dehydration of imidazole glycerol phosphate to imidazole acetol phosphate, the sixth step of histidine biosynthesis in plants and microorganisms where the histidine is synthesized de novo. There is an internal repeat in the protein domain that is related by pseudo-dyad symmetry, perhaps as a result of an ancient gene duplication. The apo-form of IGPD exists as a catalytically inactive trimer which, in the presence of specific divalent metal cations such as manganese (Mn2+), cobalt (Co2+), cadmium (Cd2+), nickel (Ni2+), iron (Fe2+) and zinc (Zn2+), assembles to form a biologically active high molecular weight metalloenzyme; a 24-mer with 4-3-2 symmetry. Each 24-mer has 24 active sites, and contains around 1.5 metal ions per monomer, each monomer contributing residues to three separate active sites. IGPD enzymes are monofunctional in fungi, plants, archaea and some eubacteria while they are encoded as bifunctional enzymes in other eubacteria, such that the enzyme is fused to histidinol-phosphate phosphatase, the penultimate enzyme of the histidine biosynthesis pathway. The histidine biosynthesis pathway is a potential target for development of herbicides, and IGPD is a target for the triazole phosphonate herbicides.	1.79995e-63
NZ_CP022203.1\|WP_013940830.1\|5165200_5165962_-\|imidazole-glycerol-phosphate-synthase-subunit-HisF	gnl\|CDD\|234996	PRK02083, PRK02083, imidazole glycerol phosphate synthase subunit HisF; Provisional.	4.29796e-151
NZ_CP022203.1\|WP_095959340.1\|5146109_5150369_-\|ribonuclease-R	gnl\|CDD\|273947	TIGR02063, Ribonuclease_R, ribonuclease R. This family consists of an exoribonuclease, ribonuclease R, also called VacB. It is one of the eight exoribonucleases reported in E. coli and is broadly distributed throughout the bacteria. In E. coli, double mutants of this protein and polynucleotide phosphorylase are not viable. Scoring between trusted and noise cutoffs to the model are shorter, divergent forms from the Chlamydiae, and divergent forms from the Campylobacterales (including Helicobacter pylori) and Leptospira interrogans. [Transcription, Degradation of RNA].	0
NZ_CP022203.1\|WP_095959337.1\|5144065_5144854_+\|hypothetical-protein	gnl\|CDD\|276809	sd00006, TPR, Tetratricopeptide repeat. The Tetratricopeptide repeat (TPR) typically contains 34 amino acids and is found in a variety of organisms including bacteria, cyanobacteria, yeast, fungi, plants, and humans. It is present in a variety of proteins including those involved in chaperone, cell-cycle, transcription, and protein transport complexes. The number of TPR motifs varies among proteins. Those containing 5-6 tandem repeats generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein. It has been proposed that TPR proteins preferentially interact with WD-40 repeat proteins, but in many instances several TPR-proteins seem to aggregate to multi-protein complexes.	5.09152e-06
NZ_CP022203.1\|WP_095959349.1\|5163816_5164425_-\|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE	gnl\|CDD\|235067	PRK02759, PRK02759, bifunctional phosphoribosyl-AMP cyclohydrolase/phosphoribosyl-ATP diphosphatase HisIE.	1.93368e-86
NZ_CP022203.1\|WP_095959344.1\|5154961_5156053_-\|lipoyl(octanoyl)-transferase-LipB	gnl\|CDD\|319743	cd16444, LipB, lipoyl/octanoyl transferase. Lipoate-protein ligase B is a octanoyl-[acyl carrier protein]-protein acyltransferase the catalyzes the first step of lipoic acid synthesis. It transfers endogenous octanoic acid attached via a thioester bond to acyl carrier protein (ACP) onto lipoyl domains, which is later converted by lipoate synthase LipA into lipoylated derivatives.	2.33527e-97
NZ_CP022203.1\|WP_095959339.1\|5145842_5146061_-\|DUF3185-family-protein	gnl\|CDD\|378652	pfam11381, DUF3185, Protein of unknown function (DUF3185). Some members in this bacterial family of proteins are annotated as membrane proteins however this cannot be confirmed. Currently no function is known.	2.74006e-14
NZ_CP022203.1\|WP_095959350.1\|5164424_5165204_-\|histidinol-phosphatase	gnl\|CDD\|273949	TIGR02067, his_9_HisN, histidinol-phosphatase, inositol monophosphatase family. This subfamily belongs to the inositol monophosphatase family (pfam00459). The members of this family consist of no more than one per species and are found only in species in which histidine is synthesized de novo but no histidinol phosphatase can be found in either of the two described families (TIGR01261, TIGR01856). In at least one species, the member of this family is found near known histidine biosynthesis genes. The role as histidinol-phosphatase wsa first proven in Corynebacterium glutamicum. [Amino acid biosynthesis, Histidine family].	6.47286e-101
NZ_CP022203.1\|WP_013940819.1\|5153414_5154089_+\|GTP-cyclohydrolase-II	gnl\|CDD\|234745	PRK00393, ribA, GTP cyclohydrolase II RibA.	6.86635e-107
NZ_CP022203.1\|WP_095959346.1\|5157970_5159236_-\|2-oxo-acid-dehydrogenase-subunit-E2	gnl\|CDD\|237001	PRK11856, PRK11856, branched-chain alpha-keto acid dehydrogenase subunit E2; Reviewed.	1.9835e-175

>NZ_CP022203.1|WP_095959344.1|5154961_5156053_-|lipoyl(octanoyl)-transferase-LipB
MNTITVYRLGRVEYEDGLELMRLFSESRREGLSGDVLLLLEHPPILTLGRAAKRENIVASDARLAQEGAEVFETNRGGDVTYHGPGQLVGYPLFLLPEDRRDVRRYVRDVERSVMQVLARWGITAGPIPKWPGVWIGEEGAPDARKVAAIGVHLSRWLTTHGFALNVNTNLDHFQLIVPCGIREAGVTSMQRELGRALPMAEVEDAIADSFCAVFDSERVDAPEPMRTVSIAVVKGHGPEARVLLVRRRPERGGFWQVLTGRLEAGESPARAAARELEEETGLRAPLVDLTYRHAFALGDALPPRLVEEHGFAVQVPPDADVRLGAEHDTFEWVDVPTALERLPFRGLRETVKRAVAGTGPTA
>NZ_CP022203.1|WP_095959343.1|5154150_5154972_+|MBL-fold-metallo-hydrolase
MRFWGVRGSIPSPGARTQRYGGNTPCVEVRCGEELLIFDLGTGARALGHALLAKKQPVKGSIFISHYHYDHLQGLPFFGPMFLPTSTLTIYGPSRHGQSVKQLLSGQMVPPYFPVTADGVFRARLSYTDLAATQTLELGPATVRTIELNHPGGNLGYRVECQGRSVVYATDLEHGTDMDAAFYDFARDADVLIYDAMYTEDEYHGRTGPARTGWGHSTWQAAVRAADEAGVKKLVLFHHDPSRDDAGMDRLLRQVRKHRPDAIAARESLVLKL
>NZ_CP022203.1|WP_013940819.1|5153414_5154089_+|GTP-cyclohydrolase-II
MSDIRSPQVLPTRKPTQHLERFSEADIPTERGTLRTIVFRDKRNGREHVALVVGQVSGDEGVPVRIHSECLTSEVFGSLKCDCREQLDRSLDFIAQAGQGVVLYLRQEGRGIGLGNKIKAYALQAKGLDTYEANRQLGFADDLRTYDIAAEMLRSLDVRSVDLMTNNPLKIAGMVEEGIPVRRRIPSRTEHNPHNVDYLRTKRERTGHLIELFAEDDDTEAKAG
>NZ_CP022203.1|WP_095959342.1|5152064_5153297_+|molybdopterin-molybdotransferase-MoeA
MNDSATLRPEEDARSQILALCAPLPSEWLPLDDALGRVLAEDVTAQRTLPPWDNSAMDGYAVRSADLGGPLPVRLDVGETLYAGGTPQRPLVAGVCARIMTGAPLPEGADAVVMRERTRPAVRGGADQVDVLEAARPGQFVRPRGEDAREGQLLLARGTPLGIPELGLLWAQGRQAVPVARAPRVAILSTGDELCHADEPPNGRIVDTNAPSLALAVRRAGGVPTLLGIARDTRDAVAAALSGLEGFDVVLTSAGVSVGERDYVKEVLAALGVEQHFWRVAIKPGKPLLVGRRGATLFFGLPGNPTSSLVTFELFVRPALRRLLGHSQVAPGRVPGRLEGRLTKPAGLAHFVRVTAAWREGNLWARPLATQTSGVLRSATAATHLLHFPREASSLSEGDTVELLPLSWVA
>NZ_CP022203.1|WP_095959341.1|5150477_5151869_-|protease-inhibitor-I42-family-protein
MAKPKSGAKKTTPAGKAGAKPAAKKDSAARLDLIKNASKRVAKAATKLAKAASDVTKGAKGAVKKAAQEKATAKKAAPAGKTASAAKAAPAAKAPKAPPAKAPPSKAPPAAKAAAGAKTAKASAVPVAPPVERPRPRATKLPPPGDPLTKREMEQLLTAGEGRGVTGEGSLKGRLVVTNDLPHLVVVGRDKRELTFLLQGPDQEVLPAYVDHKVSVSGLIRKTTNHGGVVDVRKYSAKKPDAEAVEAAPAETEERLRYLSPGEVSMVTAAGMGAGIKGFAGVRGNLEMTGEEFVLVVSNGGTRQQVSFIIEGKAAGKPLRKHVGHTLQVQGVVDKTSGWGGRIAAENVEPRPSEARAVSRDEMELVHIEGEVPTSVDVRLNHGLTVRLPEQPGFTWAIEPTVAKRVGLREANFEPAPEDGPGTREFFFTPRNPGTFEVEFFLAKALSPGLVDRTFKINVTVKP
>NZ_CP022203.1|WP_095959340.1|5146109_5150369_-|ribonuclease-R
MSLSPDLLKQLLAEADHPLGIKELLRLAGLHPGQQTELKRTLRELVRQGDILKEGKRFVPRQPSRREADARAREPGAPEAWRQRTAGGFRDGASGRGARHTPPRVGPGGYAARRQEGDARGKGSGWQERGPGRERRGAPKQGGGFRRERAERPGRRGRFSEAEGQDLLEGILHVHRDGFGFVHPSSGEGDNVFLPPHEAQRALDNDRVVVAVSGRPPRLEGRLVRVVQRRRELAVGTYVVKGRYAVVYPTDSSLPGPIRVPLTQMAREGDLVKVQLGIGAQMLDPDRGLHGEVAGSLGKPGTPGAEVLGVAYSQGFSDEFPPEVMSEADRYAVRVSDEEARGEQRRDLRAMPLITIDGEDARDFDDAVYVEDRPDGWRLVVAIADVSHYVWEGSALNTEALRRATSVYLPDRVLPMLPERLSNGICSLRPDEDRLCMVADMTYDRRGHRQSHDLYPAVMRSAARCTYNEVQDVLDGKDVPHRNALKPHFERLMALARALMKMRKERGAIDFDLPEHKVVLGEDGLPERMDKRERKDSHRLIEECMLAANEAVAMFFQDEGLPTVYRFHGEPDPEKLATFAALAEAYGFKMRVEDGVASKELDAFISQLQGHPEQRALNQLLLRSMMQAIYTSSRVGHYGLAAEHYLHFTSPIRRYPDLLVHRLLKAHWARRGRKPSPSMLEREEDQLEDMAAQCSERERAAMQVEREVVSFYACLMMKDRVGEEFAATVAAITDFGFFVELDEEHVEGLVKAETLGPGAKLDKLTHSLVYANGRRVRVGQKLRVRLTSVNVTAKKIDFEALQFEGEAPLSRAGTAGAQPHRRQAWMAEAPSHRERGGRREQREQRPGRREREAAGRGPSQGTREEMDAGRPRGRFSRDGRREEAAPHRNEPRFPPRAPEGQGTQPTESPAWSKRRTFIRPEPPVAAPVAETAAPRPPEAPSAPAPWEVPTGEEGARSPHPGFDRIRALAAQRHGGADTRGAGPGRPHAKQKPQGGPGPRYPAPKPRPPSEDGKAFSMEPPRPPPEDEQAFSMEPPRPQPEARVEAPARVLAPAHVKAEPAAPTPVAEGPVSSAPTRVDRPKAAEPANEAPAQKGQAAEVKSAALKAERTPPRQEVGEGASRNAKDKNAAPTQAATAAGAKAAVSAPAKKAAGVKAAVSAPAKKAAGTAAVSTPAKKAAGTAAVSTPGKKAARKAQVQVPAKKAAGTAAVSTPGKKAVTSKATVSAPAKKAAAPEAQVKVSAKQAIASRATANVPAKKAVTSKATVSAPAKKAAAPEAQVQVPAKQATASRATVNVPAKKAVTSKATVGAPAKKAAAPEAQVKVSSKEAAAPKAPVKVPTKKAAAPEAQVKVSSKEAAAPKAPVKVPTKKAAVPKAQVKVPAKQAKASGAAKQAKASGAAKQAKASGAAKKQGPSGSKKR
>NZ_CP022203.1|WP_095959339.1|5145842_5146061_-|DUF3185-family-protein
MSFVRLLGVMLAIAGAVLLWSGLKARDSLAERATELFTGRNTDRTTLYLAGGGAALAGGLLMMLAGGGRRRR
>NZ_CP022203.1|WP_095959338.1|5145070_5145814_+|DUF2807-domain-containing-protein
MHIAKSGGWVGTALLAVALAACSTGPFVDGNGQRTESERDTPAFEEVHVGDGVEATVVVEPDQPARVIVEGDSNLVELLRTEVKPGARLRVYFREEDVGHWESVHPLRVRITVPTLKSFRRSGGGASDLSGRIDVPAFLLTASGGGTIRARGFVTERLTLETSGGTETTLEGQATRLDSEMSGGGRLFATGLQTRDARLESSGGGTSEVQVSDTLRVEASGGADIRIIGAPTVVDRDLSGGSRLHFD
>NZ_CP022203.1|WP_095959337.1|5144065_5144854_+|hypothetical-protein
MKRLGKVGLVVGALALGGMAVGCKAEDDTAKKHRIAGSNHLSKKEYKEAAAAYALSLQADPKQEKVWEKKAFAHMQLGQMNEAAEAVLKMGEMKTEPAEKAELYRTLASMYMTGGTTEEAEKYFNEALKLEPKDEASLGWIAEIYAQRGGARSMGAPIIKESLEKSLSYYDQVIAINPNSANTYLNKRVVMGRLMEFERQQKEMALSEATENAKDKAIVAEATARAEEHQKRMDEYQVQFAEMTKKFGEAQKAAKAQAAEAK
>NZ_CP022203.1|WP_095959336.1|5142702_5143917_+|metallophosphoesterase
MPLRLFSFSMLIGLGALLGHLYLYRRLVRPLVQGRWPRLMALGVLVAMTGVLGFRRTVLDLLPESAEGLLNMAMYTWMGVALCLVIALLVTDVGRGLAALARRLRPAARPEAPLPAPAASASSPNVDEERRRFLGQAVAGGAFVAGGGLASYGSWRAFSPPLVTEVAVKVPKLPRALDGLSIVQLTDIHVGHFIQRKYMDALVQQANALRPDLFAITGDLVDGDVASLGGHVSALAALKSRYGSYFVTGNHDYYSGDEAWTAFLESLGIEVLRNRHVRIGDAGASLDLVGVDDWSGGRRRNKQGYDLDQALAGRDPDRAAVLLAHQPANFKVAAERGVDLQISGHTHGGQLAPMTFLISLAWEHSAGLYGHGDSSIYVSRGCGFWGPPMRVGSPPEIVKLVLTA
>NZ_CP022203.1|WP_095959346.1|5157970_5159236_-|2-oxo-acid-dehydrogenase-subunit-E2
MAIFEFKLPDLGEGVMEGELVKWHVKAGDSVKEDQVLAEVMTDKATVTVPAPKAGRVVQTHGKEGDMAKVHQLLVTLEVEGDAPAQAGGHGEASAPAAAPVAAAPAAGGNGGGAPASSSKVLATPVTRRMAREHGLDLSAIPGTGPQGRVTKADVVAALEGGEKNVVAAPAAQQARPAAPPVSSGASDERIPLRGLRKKIAEKMVRSKFTAPHFAFVEEVDATDLVALRARLNAQLAAAGENLKLNYLPFIIKATVAALKKFPHLNANFDEARQELVVRGEFNIGMAAATPDGLTVAVVKNADRLTLGELARETARLGAAARDRKLKMEELTGGTFTISSLGQSGGLFATPIINHPEVGILGVHRLKKRPAVVGDQVVVRDMMNLSLSCDHRVIDGSVAADFTYEIIKYLEKPDLLFLAMA
>NZ_CP022203.1|WP_013940824.1|5159296_5160226_-|lipoyl-synthase
MATPDRFPLPQVTETTRKPEWLKVRLPHGDGYERVKAIVKRTKLATVCEEARCPNIAECWGGGTATVMLMGEVCTRACRFCHVKVGAPPPLDPMEPIHLAQAVKEMNLEYIVVTSVNRDDRPDGGASHFASAIRELRRESPRTIVEVLIPDFKGVEKDLTTVAEAKPHVVAHNVETVERLTPTVRDRRAHYRQSLRVLEYLKRRPEGLYTKTSVMVGLGETDAELEQTFKDLRDVGVDVLTLGQYLQPSQYHLRVERFVTPAQFEAYKALAESYGFLYVASGPLVRSSYRAAEFFMKGLMERERLERLG
>NZ_CP022203.1|WP_095959347.1|5160484_5161882_-|dihydrolipoyl-dehydrogenase
MAETFDVVIIGSGPGGYVGAIRAGQLGLKTAIIEKDKRLGGTCLHRGCIPTKSLLWTAELFHHVREAADFGIDVSSPAINWPNAMKHKDKVVTKGANGIDFLMKKNKVTVVKGHGRIAGKGKVEVTAEDGSKQVLEAKNIIIATGSVPKSLPNVPVDHKRVLNSDSILQIDRVPKSIIVLGAGAVGCEFASVFNHVGSKTAIVEYMPALLPIEDADISKELEKIFKRRGIDVHTGSAVEKVEHTADGVRVTMKVGNETKTLEAEILLSAVGRSPVTEDVGLDKTSIKSERGYIKVDSMLRTSEPNVYAVGDIIPTPMLAHMASAECVVAVEHIAGKSPQPINYDLTPSATYCYPEVASVGLTEKKAKERGYDVKVGIAPMGAVTKAAISNEATGMIKIVSDRKYDEVLGVHIIGPHATELLAEACVALKLEITTEELANTIHAHPTLSEIVHEGAEATLGHPRHF
>NZ_CP022203.1|WP_095959348.1|5161899_5163087_+|hypothetical-protein
MRMEPGGADNPRSRLESRSLLVRRFPLRTVLLMLVALIAFGRLWCVTHPEEAPSPPPERLTRAPGGPGPAAAPECRTLERALESALRAPQDAQVQESARGRLDACGQPPVRACALGPALDARSPLSEGEATPLRGLLATLCERCPAAVNPCAQAVGQALLSAAVGPNVDAASARWNLAHAGAGTGGACASLVQLGLAPAAQSGITVRPPVRSLVGELAPLCSRAGHLDDALLRAAAANLVAPTPSLVALAAAPTPPETGPVEPDRTEGTEPGHQAFDRDEHTGVAVGMALRGERWEADGALRASYAPTLKQLVSVSVRATGPGTVRAIVRTPQGVGLKDPEKGFAFVNPTVCRFNGTGQWEQCPLPVPLRDVDAVSVFPERADTELKELEVHGAR
>NZ_CP022203.1|WP_013940827.1|5163101_5163551_-|hypothetical-protein
MNGPTYKAEIIDRVIFSRWENPPTKEDVTLVLAQMQEAASRLNTNLIYVGSVSSKSKVPDANERTVLNQFLMDARRTCVEQAWLIYEGTDLQHNLQRVIISGVLILTRTFDNFLSVAKSGDSIIKDVSAVLKKDAAPLFTLARERGLLV
>NZ_CP022203.1|WP_095959349.1|5163816_5164425_-|bifunctional-phosphoribosyl-AMP-cyclohydrolase/phosphoribosyl-ATP-diphosphatase-HisIE
MLDLDSLDFTKGNGMVTVVTQDARTGDVLMVAHADREALERTLATGEMHYRSRTRGLWHKGATSGNVQRVVALRADCDGDAVLARVEKAGPACHTGEETCFGPGRWDALAALDDTLARRAAPEPPSGDAPPSYTRRLMDDRNLRLKKLGEEAAELVTACADADPRRAVEEAADLLYHVLVAVRPLGLTLDDVKAVLARRAAR
>NZ_CP022203.1|WP_095959350.1|5164424_5165204_-|histidinol-phosphatase
MTNAGNLMQAAAELARTAGDVALGFFRAGIAVDTKSDGSPVTVADRTAESRAREWLEARFPEDGILGEEFGETRPGARRRWILDPIDGTKTFIRGVPLWGTLVALAEGERVLVGAAYFPAVGELLVAAPGQGCFWNDQPTRVSTQAELARAVVLSTDERFPVYPERGAAWRALARDAAVDRTWGDCYGYLLVATGRAEVMVDELLSPWDGAALQPIIEEAGGVFTDWTGKRTAFGGNGIATNAALARVVRERLGAVEAR
>NZ_CP022203.1|WP_013940830.1|5165200_5165962_-|imidazole-glycerol-phosphate-synthase-subunit-HisF
MLTRRLVVCLDVKGGRVVKGVQFEGLRDVGDPVALARRYEAEGADEVTFLDISASAEERGTLWELVRRTAEQLFIPLAVGGGVRTVEDVGRALRAGADKVSINSAAVANPALLTACAERFGAQCVVASIDAKRDGDRWRVYTHGGRKPTDLDAVAWARECVARGAGEVLLTSIDRDGARRGYDVALTRAVSEAVDVPVIASGGAGDAAHVRDAFHEGGADAALVAGILHDGLTTVGAIKSLLRESGLHIRSVT
>NZ_CP022203.1|WP_095959351.1|5165961_5166498_-|imidazoleglycerol-phosphate-dehydratase
MTTVIRETKETQVHVEVTPGKGATQVDTGLKFFDHMLATFARYAGLDLTLRARGDLTHHVMEDVAITLGTAVQRVIPATAARFAERTIPMDDALVQACLDAGGRFYYQGPLKNRLYEHWMRSFCEHARVTLHLRVLRGKDSHHATEAAFKALGLALRDAMVDSGSVFSMKGSVALEVK
>NZ_CP022203.1|WP_095959352.1|5166494_5167211_-|1-(5-phosphoribosyl)-5-[(5--phosphoribosylamino)methylideneamino]-imidazole-4-carboxamide-isomerase
MIAIPAIDLREGACVQLVGGSYAAERVRVDDPLEALKQWRAHGFSAFHVVDLDAALGKGSNADAIFRLTAYERGLTFTVGGGVRDSDRVEAVLSGGAACAVVGTRAIEDGAWLADVASRYPGRVVVAADVKGREVVTRGWTEGSRRDIRDVLAAFEPLPLGGLLVTAVHKEGQLSGVDLPLMREVASTSRHRLYASGGVTTLEDLRALAAAGAYGAVIGMALYTGRLDASAVAREFAG

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Crispr_ID: NZ_CP022203_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_11

5516602-5517119

Orphan

Consensus_repeat	Method
GNNNCCGGCGGNNNCNCN	CRT

10 spacers

The CRISPR arrays of NZ_CP022203_11

>merge|NZ_CP022203|11|5516602-5517119|CRT
GGAGGCTGCGGCACGCCCGCGGGCGGACGGAACCCACCCGGCGCGGGCCCCCCGGCGGAGGCGGCACGCCCGGACGCGCCATGGCGCCCGGCCCCGGCGGCATGCCCGGACGCGGCGGCAGCCCCGCCCCAGGCCCCCCGGCGGAGGCGGCACACCCGGACGCGCCCCCGGCGGCATCCCAGGCCCCGGCGGACGCGCACCCGGCGGCATCCCAGGCCCCGGCGGACGCGCCATGCCCGGAGGCGGCACCCCAGGCCCCGGCGGACGCGGCGCGCCCGGGGCGCCCGGAGGCGGCATGCCGGGCCCCGGCGGACGCGCCATGCCCGGAGGCGGCGCGCCCGGCGGACGCGCACCCGGCGGCGGCATGCCCGCGCCCGGCGGACGCGGCACGCCCGGCCCCGGCGGAACCCCCGGACGGGCGCCCGGCGGCGGCGCGGGACGGGCGCCCGGCGGCACGGCGCCAGCGACGGGCGCGGGCGCGGGCGCGGCGGGCGCCGGCTGCGGCGCGGCGGGGCGCA

>NZ_CP022203|11|4|5516602-5517119|CRT
GGAGGCTGCGGCACGCCC	GCGGGCGGACGGAACCCACCCGGCGCGGGCCCCCC
GGCGGAGGCGGCACGCCC	GGACGCGCCATGGCGCCC
GGCCCCGGCGGCATGCCC	GGACGCGGCGGCAGCCCCGCCCCAGGCCCCCCGGCGGAGGCGGCACACCCGGACGC
GCCCCCGGCGGCATCCCA	GGCCCCGGCGGACGCGCACCCGGCGGCATCCCA
GGCCCCGGCGGACGCGCC	ATGCCCGGAGGCGGCACCCCA
GGCCCCGGCGGACGCGGC	GCGCCCGGGGCGCCCGGAGGCGGCATGCCG
GGCCCCGGCGGACGCGCC	ATGCCCGGAGGCGGCGCGCCCGGCGGACGCGCACCCGGCGGCGGCATGCCC
GCGCCCGGCGGACGCGGC	ACGCCCGGCCCCGGCGGAACCCCCGGACGG
GCGCCCGGCGGCGGCGCG	GGACGGGCGCCCGGCGGCACGGCGCCA
GCGACGGGCGCGGGCGCG	GGCGCGGCGGGCGCCGGCT
GCGGCGCGGCGGGGCGCA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095959522.1\|5509319_5510972_+\|alkaline-phosphatase-family-protein	unknown	unknown	gnl\|CDD\|293740
NZ_CP022203.1\|WP_013941058.1\|5507835_5508801_-\|class-II-fructose-bisphosphatase	unknown	unknown	gnl\|CDD\|236536
NZ_CP022203.1\|WP_095959520.1\|5505628_5506672_+\|ADP-ribosylglycohydrolase-family-protein	unknown	unknown	gnl\|CDD\|377122
NZ_CP022203.1\|WP_157757532.1\|5511956_5513144_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235334
NZ_CP022203.1\|WP_013941057.1\|5507367_5507793_-\|SRPBCC-family-protein	unknown	unknown	gnl\|CDD\|176854
NZ_CP022203.1\|WP_095959531.1\|5526438_5527416_-\|NAD-dependent-epimerase/dehydratase-family-protein	unknown	unknown	gnl\|CDD\|187540
NZ_CP022203.1\|WP_013941067.1\|5519884_5520277_-\|demethoxyubiquinone-hydroxylase-family-protein	unknown	unknown	gnl\|CDD\|275328
NZ_CP022203.1\|WP_095959525.1\|5518504_5519878_+\|diguanylate-cyclase	unknown	unknown	gnl\|CDD\|143635
NZ_CP022203.1\|WP_013941056.1\|5506777_5506954_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_157757533.1\|5520427_5521945_+\|hybrid-histidine-protein-kinase/response-regulator-SinK	unknown	unknown	gnl\|CDD\|223715
NZ_CP022203.1\|WP_095959523.1\|5511112_5512006_-\|carboxylating-nicotinate-nucleotide-diphosphorylase	unknown	unknown	gnl\|CDD\|238806
NZ_CP022203.1\|WP_095959521.1\|5508831_5509260_-\|acyl-CoA-thioesterase	unknown	unknown	gnl\|CDD\|223894
NZ_CP022203.1\|WP_095959519.1\|5504223_5505522_-\|phosphopyruvate-hydratase	unknown	unknown	gnl\|CDD\|234617
NZ_CP022203.1\|WP_013941053.1\|5503430_5504219_-\|5'/3'-nucleotidase-SurE	unknown	unknown	gnl\|CDD\|234732
NZ_CP022203.1\|WP_043711626.1\|5517638_5518454_-\|chemotaxis-protein-CheW	unknown	unknown	gnl\|CDD\|366716
NZ_CP022203.1\|WP_095959529.1\|5524965_5525364_-\|response-regulator	unknown	unknown	gnl\|CDD\|381103
NZ_CP022203.1\|WP_095959532.1\|5527463_5528162_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP022203.1\|WP_095959530.1\|5525366_5526485_+\|metallopeptidase-family-protein	unknown	unknown	gnl\|CDD\|240572
NZ_CP022203.1\|WP_095959527.1\|5521941_5523027_+\|signal-integration-modulator-SinM	unknown	unknown	gnl\|CDD\|225921
NZ_CP022203.1\|WP_095959528.1\|5523156_5524797_-\|chaperonin-GroEL	unknown	unknown	gnl\|CDD\|234573

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095959522.1\|5509319_5510972_+\|alkaline-phosphatase-family-protein	gnl\|CDD\|293740	cd16016, AP-SPAP, SPAP is a subclass of alkaline phosphatase (AP). Alkaline phosphatases are non-specific phosphomonoesterases that catalyze the hydrolysis reaction via a phosphoseryl intermediate to produce inorganic phosphate and the corresponding alcohol, optimally at high pH. Alkaline phosphatase exists as a dimer, each monomer binding 2 zinc atoms and one magnesium atom, which are essential for enzymatic activity. Although SPAP is a subclass of alkaline phosphatase, SPAP has many differences from other APs: 1) the catalytic residue is a threonine instead of serine, 2) there is no binding pocket for the third metal ion, and 3) the arginine residue forming bidentate hydrogen bonding is deleted in SPAP. A lysine and an asparagine residue, recruited together for the first time into the active site, bind the substrate phosphoryl group in a manner not observed before in any other AP.	1.1181e-87
NZ_CP022203.1\|WP_013941058.1\|5507835_5508801_-\|class-II-fructose-bisphosphatase	gnl\|CDD\|236536	PRK09479, glpX, fructose 1,6-bisphosphatase II; Reviewed.	0
NZ_CP022203.1\|WP_095959520.1\|5505628_5506672_+\|ADP-ribosylglycohydrolase-family-protein	gnl\|CDD\|377122	pfam03747, ADP_ribosyl_GH, ADP-ribosylglycohydrolase. This family includes enzymes that ADP-ribosylations, for example ADP-ribosylarginine hydrolase EC:3.2.2.19 cleaves ADP-ribose-L-arginine. The family also includes dinitrogenase reductase activating glycohydrolase. Most surprisingly the family also includes jellyfish crystallins, these proteins appear to have lost the presumed active site residues.	1.82535e-31
NZ_CP022203.1\|WP_013941057.1\|5507367_5507793_-\|SRPBCC-family-protein	gnl\|CDD\|176854	cd07812, SRPBCC, START/RHO_alpha_C/PITP/Bet_v1/CoxG/CalC (SRPBCC) ligand-binding domain superfamily. SRPBCC domains have a deep hydrophobic ligand-binding pocket; they bind diverse ligands. Included in this superfamily are the steroidogenic acute regulatory protein (StAR)-related lipid transfer (START) domains of mammalian STARD1-STARD15, and the C-terminal catalytic domains of the alpha oxygenase subunit of Rieske-type non-heme iron aromatic ring-hydroxylating oxygenases (RHOs_alpha_C), as well as the SRPBCC domains of phosphatidylinositol transfer proteins (PITPs), Bet v 1 (the major pollen allergen of white birch, Betula verrucosa), CoxG, CalC, and related proteins. Other members of this superfamily include PYR/PYL/RCAR plant proteins, the aromatase/cyclase (ARO/CYC) domains of proteins such as Streptomyces glaucescens tetracenomycin, and the SRPBCC domains of Streptococcus mutans Smu.440 and related proteins.	5.93983e-18
NZ_CP022203.1\|WP_095959531.1\|5526438_5527416_-\|NAD-dependent-epimerase/dehydratase-family-protein	gnl\|CDD\|187540	cd05229, SDR_a3, atypical (a) SDRs, subgroup 3. These atypical SDR family members of unknown function have a glycine-rich NAD(P)-binding motif consensus that is very similar to the extended SDRs, GXXGXXG. Generally, this group has poor conservation of the active site tetrad, However, individual sequences do contain matches to the YXXXK active site motif, and generally Tyr or Asn in place of the upstream Ser found in most SDRs. 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. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. 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. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.	1.84931e-107
NZ_CP022203.1\|WP_013941067.1\|5519884_5520277_-\|demethoxyubiquinone-hydroxylase-family-protein	gnl\|CDD\|275328	TIGR04535, conserved_hypothetical_protein, ferritin-like protein. Two families of proteins are known to be encoded, with some regularity, next to the gene for encapsulin (pfam04454), with surrounds the target protein to form a prokaryotic proteinaceous organelle. One is the family of enzymes that includes Dyp-type peroxidases. The other is this family, with a resemblance to bacterioferritins. Encapsulin-associated forms of the proteins in these two families have a necessary C-terminal motif that resembles DGSL[SGN]IGSL[KR]. Members of this family that include the last columns of the model in the hit region (and are encoded next to the encapsulin gene) should be designated encapsulin-associated ferritin-like protein.	1.01588e-19
NZ_CP022203.1\|WP_095959525.1\|5518504_5519878_+\|diguanylate-cyclase	gnl\|CDD\|143635	cd01949, GGDEF, Diguanylate-cyclase (DGC) or GGDEF domain. Diguanylate-cyclase (DGC) or GGDEF domain: Originally named after a conserved residue pattern, and initially described as a domain of unknown function 1 (DUF1). This domain is widely present in bacteria, linked to a wide range of non-homologous domains in a variety of cell signaling proteins. The domain shows homology to the adenylyl cyclase catalytic domain. This correlates with the functional information available on two GGDEF-containing proteins, namely diguanylate cyclase and phosphodiesterase A of Acetobacter xylinum, both of which regulate the turnover of cyclic diguanosine monophosphate. Together with the EAL domain, GGDEF might be involved in regulating cell surface adhesion in bacteria.	5.8381e-56
NZ_CP022203.1\|WP_157757532.1\|5511956_5513144_-\|hypothetical-protein	gnl\|CDD\|235334	PRK05035, PRK05035, electron transport complex protein RnfC; Provisional.	2.54974e-14
NZ_CP022203.1\|WP_157757533.1\|5520427_5521945_+\|hybrid-histidine-protein-kinase/response-regulator-SinK	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.29344e-34
NZ_CP022203.1\|WP_095959523.1\|5511112_5512006_-\|carboxylating-nicotinate-nucleotide-diphosphorylase	gnl\|CDD\|238806	cd01572, QPRTase, Quinolinate phosphoribosyl transferase (QAPRTase or QPRTase), also called nicotinate-nucleotide pyrophosphorylase, is involved in the de novo synthesis of NAD in both prokaryotes and eukaryotes. It catalyses the reaction of quinolinic acid (QA) with 5-phosphoribosyl-1-pyrophosphate (PRPP) in the presence of Mg2+ to produce nicotinic acid mononucleotide (NAMN), pyrophosphate and carbon dioxide. QPRTase functions as a homodimer with two active sites, each formed by the C-terminal region of one subunit and the N-terminal region of the other.	2.46962e-127
NZ_CP022203.1\|WP_095959521.1\|5508831_5509260_-\|acyl-CoA-thioesterase	gnl\|CDD\|223894	COG0824, FcbC, Predicted thioesterase [General function prediction only].	5.50665e-42
NZ_CP022203.1\|WP_095959519.1\|5504223_5505522_-\|phosphopyruvate-hydratase	gnl\|CDD\|234617	PRK00077, eno, enolase; Provisional.	0
NZ_CP022203.1\|WP_013941053.1\|5503430_5504219_-\|5'/3'-nucleotidase-SurE	gnl\|CDD\|234732	PRK00346, surE, 5'(3')-nucleotidase/polyphosphatase; Provisional.	5.44959e-132
NZ_CP022203.1\|WP_043711626.1\|5517638_5518454_-\|chemotaxis-protein-CheW	gnl\|CDD\|366716	pfam01584, CheW, CheW-like domain. CheW proteins are part of the chemotaxis signaling mechanism in bacteria. CheW interacts with the methyl accepting chemotaxis proteins (MCPs) and relays signals to CheY, which affects flageller rotation. This family includes CheW and other related proteins that are involved in chemotaxis. The CheW-like regulatory domain in CheA binds to CheW, suggesting that these domains can interact with each other.	1.19628e-06
NZ_CP022203.1\|WP_095959529.1\|5524965_5525364_-\|response-regulator	gnl\|CDD\|381103	cd17551, REC_RpfG-like, phosphoacceptor receiver (REC) domain of cyclic di-GMP phosphodiesterase response regulator RpfG and similar proteins. Cyclic di-GMP phosphodiesterase response regulator RpfG, together with sensory/regulatory protein RpfC, constitute a two-component system implicated in sensing and responding to the diffusible signal factor (DSF) that is essential for cell-cell signaling. RpfC is a hybrid sensor/histidine kinase that phosphorylates and activates RpfG, which degrades cyclic di-GMP to GMP, leading to the activation of Clp, a global transcriptional regulator that regulates a large set of genes in the DSF pathway. RpfG contains a CheY-like receiver domain attached to a histidine-aspartic acid-glycine-tyrosine-proline (HD-GYP) cyclic di-GMP phosphodiesterase domain. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	5.89881e-26
NZ_CP022203.1\|WP_095959532.1\|5527463_5528162_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	4.57509e-15
NZ_CP022203.1\|WP_095959530.1\|5525366_5526485_+\|metallopeptidase-family-protein	gnl\|CDD\|240572	cd12952, MMP_ACEL2062, Minimal MMP-like domain found in Acidothermus cellulolyticus hypothetical protein ACEL2062 and similar protein. The subfamily includes an uncharacterized protein from Acidothermus cellulolyticus (ACEL2062) and its homologs from bacteria. Although its biological role remains unclear, ACEL2062 contains a minimal metalloprotease (MMP)-like domain consisting of 3-stranded mixed 2-beta sheets and a HExxHxxGxxD/S (x could be any amino acid) motif. It may belong to a superfamily of bacterial zinc metallo-peptidases, which is characterized by a conserved HExxHxxGxxD motif.	5.30597e-36
NZ_CP022203.1\|WP_095959527.1\|5521941_5523027_+\|signal-integration-modulator-SinM	gnl\|CDD\|225921	COG3386, COG3386, Gluconolactonase [Carbohydrate transport and metabolism].	0.00796292
NZ_CP022203.1\|WP_095959528.1\|5523156_5524797_-\|chaperonin-GroEL	gnl\|CDD\|234573	PRK00013, groEL, chaperonin GroEL; Reviewed.	0

>NZ_CP022203.1|WP_157757532.1|5511956_5513144_-|hypothetical-protein
MQGNVDLAEELKDELEAAGGVPEAADPQVQDALEKLRAGTKEGLSPADHHDLGVAYMSMGLVDDAMREFNTARAGGDAREVPAEVEETAESETAESEAAESEVAETEAAESEAAESEAAETAQTVASTAKAVVKAALAAVRKASSIAKDTVTDAASDVEPAAPVKARPAKKAAARKAPAAETEAPTRKAPAKTAATKQAAVTKASAKGAAKKAAVTKAPAKGAAKKASAQKGAAKKAAVTKAPAKGAAKKASAQKGAAKKAAAKKAPAKVAAKKGTAKAAPAKGAAKKAPSKKAPSKGAAKKAAVTKAPARGAAKKAAAKKAPAKVAAKKGAAKKGAAATRKPVKNAAGRKAPRRRLRRRRPPGRNPKRGQSPGGSRRRRAAAGLPRPAHRARSR
>NZ_CP022203.1|WP_095959523.1|5511112_5512006_-|carboxylating-nicotinate-nucleotide-diphosphorylase
MQQQDYLDRLIALALDEDLGAAGDVTSQALIPPDYEGSAELVAKEQLVLAGLEAFVRVFKTVDPNVEVELLRRDGQEIKPKMVAARCHGRMRSLLAAERTALNIVQRAAGIATLAQQAVTSVRGSKLRVLDTRKTPPGMRTVAKEAVRMGGASNHRFGLFDGVLIKDNHIAAVGGSIAEALRRAKLNGPRLCKVEIEVTNLKQLAEAIEHGADVVMLDNMDDAQIREAVKLAAGRVPLEVSGGVTLDRLPRLAKLGIDFVSMGALTHSARAMDLSLEITAAAKRPARARQAKQPKPA
>NZ_CP022203.1|WP_095959522.1|5509319_5510972_+|alkaline-phosphatase-family-protein
MLLTIPAGMVLLPMIRALLLAAALTALPALARPPRLTLVISVDALGSDVLLRNRARLKGGLGQLLNQGAFFPYARYGQAECRTAPGHTTLSTGANPWRHGIVDNRWVERSTMKRVLAFADAAHPVLEAPLTPGQDSGPAHIQVETLADRLRVATQERGKAVAVSIKSHAAIPLAGRAGQAWWFDKGVGKFVTGTWYTKAFPEWMKALNARKLPEASFGKKWELMRPASEYVGEDEGPAESDVYGLGRTFPHPLDGGLPSPGPTFYQAFAVSPDSHDLLVEAAKAAIAGEGLGKDDVPDLLAVSFSGTDLVFHEYGPYSWEMQDTLLRLDKAMSGLIAAAERAAGGRGNLVIALSADHGGAAAPEQWAATGLAAKRVNPVELANGLTQALRQQFGGDVTATLEVLDVYLGGKTHQGGAVDAAVRRAAAAWLMKHPSVVTAVASDDLLTAPDTAGYLARMRKGYFPGRSGDVLFMVKPFHLLLSTPVGTSHGTPHAYDAQVPMLFAGKGVKPGVYLEEVDPVDFAPTLAALMELGMPASAEGKPRAEALTGR
>NZ_CP022203.1|WP_095959521.1|5508831_5509260_-|acyl-CoA-thioesterase
MVEARLRVIYGDTDQMGVVYYANYFRYFEFARSEYFRARGGSYAELERSGALLPVAEASCQYKASARYDDLLVIQTTVSELRRASIVFTYALFRDGAPRTLLCTGRTRHACVGRDGRPTRLPDALIRLLESPEPSPGSPTST
>NZ_CP022203.1|WP_013941058.1|5507835_5508801_-|class-II-fructose-bisphosphatase
MDRNLAMEVVRVTEMAAIASARLMGRGNKDESDQAAVDAMRRAFDALQIDGTVVIGEGERDEAPMLYIGEKVGKRGDGAPEVDIALDPLEGTNLCAYGRPGSIAVVAMAGKGGLLNAPDTYMEKLAVGPRARGAIDLRKTPTENLRAIAEKMKVYVEDLTVVVLDRERHTDLIKEIRAAGARIRLIEDGDVAGAIATCFDNTGVEVLMGIGGAPEGVIAAAAIRATGGDMQGRLVPRNQGEIERCKTMGISDISKIYTAEELARGEVMFAASGVTTGDFLKGVRFFGGGCETHSVVMRSKTGTVRFIQSVHKFDKKPGYAF
>NZ_CP022203.1|WP_013941057.1|5507367_5507793_-|SRPBCC-family-protein
MPGASRTIVVNAPIEKVFDVITQYEKYPEFLPEVKGIRTENRQGNTVDVHYKVDVVKTISYSIHVTEERPTRMSWSYIKGEFMKDNKGSWVLEPEGEGRTKATYTVEMALGALVPKSVVSALVETSLPKMLDAFKRRFEAP
>NZ_CP022203.1|WP_013941056.1|5506777_5506954_-|hypothetical-protein
MLDAFIIEEIKRRERRREEHDRPVVELPLPVPDERPRRRTETEDDKPQRGVVVIDLLA
>NZ_CP022203.1|WP_095959520.1|5505628_5506672_+|ADP-ribosylglycohydrolase-family-protein
MKGPDPLLAQRRRGALLGMAVGNALAVPTAHRPFMAVAFPKQAEGPYMKLMGGGPHELRRGQVTEVVQLAACLGHSLRALRRHDAADALRRYRAWQPHAFDVSEPMKEVFEDCQTSGFPPLGAGRRVWLRAHRKPATSGSLARTAPLGVYLAGDVHALVLASLEDSALTHFDPRCQLACAAFNAAIGHAVTHGAGLKATDLITAAESGLLLAGAALGRSASDYVQEVSFAAALLREDLALAQQEDPMLYGPELHLHRPAHAVRVAFRLAFWELLHAPSAEAALLDVVHRGGDTEAHAAITGALVGAFHGEQALPEEWRKQVLEALATVKGPLWEVYHPRHLLALTQG
>NZ_CP022203.1|WP_095959519.1|5504223_5505522_-|phosphopyruvate-hydratase
MTEISQILAREVLDSRGNPTVEAEVQLVGGSRGRAAVPSGASTGEHEAIELRDGDKQRYLGKGVQKAVKNVVDALAPALIGMDAADQFAVDQRMLELDGTATKGKLGANAILAVSMAAARAAADAHGLPLYRYVGGAQARTLPVPLMNILNGGAHADTRVDVQEFMVVPAGASSFAEGLRWGAEVFHALKKILKGRKLATGVGDEGGYAPDLPANEEALKLIMEAIDQAGFKAGEQLFLALDVAASEFFDKGSKKYKLKGEGKEYDSTGLLEYYRGLAERYPIISIEDGMAEDDWEGWKKLTDALGSRMQLVGDDLFVTNVERLGRGIESGTANSILVKVNQIGTLTETFDAVRMAHRAGYTSVMSHRSGETEDTTIADLAVALDCGQIKTGSASRSDRVAKYNQLLRIEGELGAAARYAGKSVFRALNQKK
>NZ_CP022203.1|WP_013941053.1|5503430_5504219_-|5'/3'-nucleotidase-SurE
MSDKPKRILVSNDDGYFSEGLQALVEAVSPLGEVWVVAPDREQSAASHAISLHRPLRIKEVRERWFAVDGTPADCAYLAINHLLKDDRPVLMVSGINHGANLAEDIMYSGTVAAAMEGALLGVPAIAFSLVARRSFDFAPGARFARSLVASALSRPLPPRMLLNVNIPGGVEPEGFVVTRQGRHSYGYEVVENEDPRGRKYYWIGGSDYQHEDIPGSDCNAVFRDKRISVTPLHFELTDHGRLPDLSGWRVDGFNRHEPDGA
>NZ_CP022203.1|WP_043711626.1|5517638_5518454_-|chemotaxis-protein-CheW
MSPFESGRRLCLLVEAGETRYAVEATSVMEVAMPGANGSSLRGVLEVKDLCALLGGPPEEGPGMVVVLDVSPTLAVRVRSVVEVADVARAPFFLLPPGLADSLAPLSRGAVLHKSRLYLELIAEALPHRVGSMAAAVSARPVHWAEAAPERALVFESQGGLFGVPLGLVSQVISRGEAFSVLPVQSGPVAGIFPHDQVLWPVCSVPALLGAEPLPEPFIVLTELAGRNVGLTATRVLGVLQRFEPDDTAGSFRAPGLSEPVAFLDLQRMFS
>NZ_CP022203.1|WP_095959525.1|5518504_5519878_+|diguanylate-cyclase
MARILLVDDEKIARTLYGDYLTAVGHAVTAVGTLQEAREALAGDRFDAVVTDLILPGGDGMEVLRHVREHHPGVEVVVITGLEKVDPAVRAIKSGAAEYLVKPVAPEALQHAVRRALTTRDLMQENASLRRHVAMLEAGQRIATTLDREKLAAATASALQSMASASAVVLLERDSAFALRRHGTSGLPTALEEPLIAELIGRLANERGTRELEGLDAPFPRAVSFPALEGDAVLGHAVLFFGGTGAEWAGETASFLVRNWALALRNLGRFAAVEDLAYVDDLTRLFNTRYLHLVVDREVQDALQSQRTFSLLFLDLDHFKSINDTHGHLVGSKVLVEAARVVKGCVRDHDVVARYGGDEYVVVLRNTDSGGALKVAERIRRTMETHNFLAREGLSLKLTTCIGVASFPEHAQDKATLLDLADRAMYRGKRGSRNVVYMAANDLEAPPAERRQAHPAT
>NZ_CP022203.1|WP_013941067.1|5519884_5520277_-|demethoxyubiquinone-hydroxylase-family-protein
MPQTNPFHSLVPRKMTDTELARSIRLNIEAELDAINLYAAHIDATDNEDAKAILQHVMDEEREHAALFWELIARLDPEQAAHAKEAVEKYRLITSGASHEAVEAVGKEGAEPSPADVTPEKRLTVGSLRR
>NZ_CP022203.1|WP_157757533.1|5520427_5521945_+|hybrid-histidine-protein-kinase/response-regulator-SinK
METPAPLAQLLQAVEAGDLTAARTAAAALQRAGAHASQLAAEVLHELRQPLLGVKAYAQLLAEDGAAPGPLRLLLSQVERMEQIVSDFIRLSSERPASQQRLSLAAPIWAAAKHFSINPDSSRISLEVEAPEDITIQGNARLIEQLTLNLLNNARDAMSGRGRVKVVLTTEGASPALYVADWGPGIPEELRARIFEPYVTANKRGTGLGLSVCQRIAREHHARLELAPPSVLRDVPPPATVFRVLFPATDAPPAQKQRLLVVDDEIIIRMVFRDLMGKECEVIEAASAEEALDLLHQAPVDLIVTDKNLPGMSGLELAQQARRLHTGSRVILMTGYPSLVTTQQALELGVVDYLLKPFDDIREVRGLLRSTLARRPAPAPLETDPAMRRVDVLEDNPAAAAQITHALTLVGLEARILTTTELAALAPPAGVVVSWDFSPAYGRKALELGKALAQGAPFVVLAEHLTMETALESLRAGAAACLPKLMSDATALSRELNRAFKREAP
>NZ_CP022203.1|WP_095959527.1|5521941_5523027_+|signal-integration-modulator-SinM
MRLALLSVLLLGVACSSDKPPTQDRRDAGTGTEDAGSEDAGSGDAGCEPLAPGLGTPLLTGLNTPRRLAVDGADLYIVESHSLNPQQPQPGPGRLLQLPRAGGDAVPVATGFRAPDALAVTPDALYVLDLDGLWRVDKATGEKDARPLDATVNNVTIGGTEVLPARLGDRDVLVIATAHRRLVRVEASGGNRQELYAGTGYTQVRGARVVGQDVWFLVAASETPGLYSVPLDGSAPATLRDGSITAGTSLEVTPTHFLVTEGGGGNGRVLRLPREGGAAEVVATDLQGPAFPVELHGTLYFKDVSTGGADFLRRVSVCSAGGAVESVGPEGVGPGGLVVDGDTLLYTSQESGTGGVVGRVP
>NZ_CP022203.1|WP_095959528.1|5523156_5524797_-|chaperonin-GroEL
MAAKEIFFHQSAREAILRGVRILSDAVAVTLGPKGRNVVIEKSFGSPTITKDGVTVAKEIDLENKFENMGAQMVKEVASKTSDKAGDGTTTATVLARAIYEEGLKLVAAGHSPMDLKRGIDKAVEVVVGELRTLSKPTADKKAITQVGTISANGDETIGVIIADAMEKVGKEGVITVEEAKGLETTLDVVEGMQFDRGYVSPYFVTNRERMEAVLDDPYILISEKKVSSMQDMIPLLEQVARAGKPLLIIADDIEGEALATLVVNKIRGVLNVCAVKAPGFGDRRKEMLQDIAVLTGGTVVSEDLGHKFETLTLTDLGRSKRATVDKDNTTIVDGVGTKAAIEGRIKLIRTQIESVTSDYDREKLQERLAKLVGGVAVINVGAATETEMKEKKARVEDALHATRAAVEEGIVPGGGVAYLRALPALEKLKLGGEQDFGVAIIVRALQEPLRKIASNAGVEGAVVINKVREGTGAFGYNARTETYEDLEKAGVIDPTKVERTALQNAASVASLLLTTEAMVAERPKGKAKAGAGAGTPDYGGDDMDY
>NZ_CP022203.1|WP_095959529.1|5524965_5525364_-|response-regulator
MLRSLARPGAALGPVNILVVDDDLELCTMLSRFLEMHGFTVYSASDALQALDVLERNQVSMVITDYVMPHMDGIQFTELLKADPRFQSVPVLLMTGSEDGSVTDRGLRKGVALTLHKPLDMGQLLTLVRFAQ
>NZ_CP022203.1|WP_095959530.1|5525366_5526485_+|metallopeptidase-family-protein
MRGVDNEVRGFICRGPMGTRTSKRAGVGGMEALDAAAVAFETGDFEAALTAADRVLAQSPDALAALHLRAAALVELGRLEEAGRAFGAALRVGPEDMEVLLGTADCLICRAGEDREAVEEGLGFCAKGKRLAQKAGDVELLFEFLLLEGMGLNQVGDCRAALTSLDAALGHLPRSVDAQVERGIALFELCRFDEAKAAFDKVLKDAPDEAWAHQYLGLLAERRGDEKEAQRRFAKAQALVPAEFFPPVELGEAEFDRAVEAAVQSLPRHAKQYLDNVTIAVEDLPADDDLLSEDPPLSPSILGVFRGLAVGERSVTNAFDHVPAAIVLYQKNLERFARTREELIEQIGITVMHEVGHLMGLDEDDLWQRGLD
>NZ_CP022203.1|WP_095959531.1|5526438_5527416_-|NAD-dependent-epimerase/dehydratase-family-protein
MGTVALFGASGVIGHSVAQALRGQGRPYRVVGRSREGLQREFGADPQAELVTWNPDDEASIRAAARGVQTLIYLVGVPYWQFRLHPILMKRTLDAAIAEGVERIVFIASVYPYGRPRTDVVNESHPRMPHTFKGRMRKEQEELLLAADKAGAIQVTILRLPDFYGPGVENSFLHRAFVAASQGKRAQLIGPIDTPHEFVYVPDVGPVVTSLIDHPGAYGRFWNLGGAGVTTQKALVEDIYAQAGVPAKYSVLGPGMVRLIGLFNPFMRELPEMHYLHATPVIMDDSALRALLGDLRKTPYHEGIRQTLAALSPAPVATGHPHPVP
>NZ_CP022203.1|WP_095959532.1|5527463_5528162_+|TetR/AcrR-family-transcriptional-regulator
MNGVHLLVAVRCVKAYTGNMGIAERKERQRAELREQILRVARDIVVKEGFPALSMRKLADAVEYAPATLYLHFENREAIAKELCVRGFQDLLALLEPAAQVEDPLERLPQLAKAYVRFGLEHPETYRLIFMEDPKLSTALFGDSPEGAGPRAFGVLVQVFVDLLAAGRLEEGTKPEQLAEVLWAGVHGIVSLRLTCTGFPGTPAEELTQVLVTTLVKGLPGLKAGRAQKKTR

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Crispr_ID: NZ_CP022203_12

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_12

6778310-6778483

Orphan

Consensus_repeat	Method
CTCGTCGCCGTCCGGCAGGCCGTCGTCGTCCGAGTCGAC	PILER-CR

2 spacers

The CRISPR arrays of NZ_CP022203_12

>merge|NZ_CP022203|12|6778310-6778483|PILER-CR
CTCGTTGCCGTCCAGGAGGCCGTCGTCGTCCGAGTCGTCATCGAGCGGATCCGTCCCCCCGACGTTCACCTCGAGGCCGTCCGGCAGGCCGTCGCCGTCCGTGTCGGGGTTGTTCGGGTCCGTGCCCAGCGCAATCTCCTCGGCGTCCGACAGGCCGTCGTCGTCCGAGTCGAC

>NZ_CP022203|12|1|6778310-6778483|PILER-CR
CTCGTTGCCGTCCAGGAGGCCGTCGTCGTCCGAGTCGTC	ATCGAGCGGATCCGTCCCCCCGACGTTCAC
CTCGAGGCCGTCCGGCAGGCCGTCGCCGTCCGTGTCGGG	GTTGTTCGGGTCCGTGCCCAGCGCAAT
CTCCTCGGCGTCCGACAGGCCGTCGTCGTCCGAGTCGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095960187.1\|6768603_6770325_+\|FHA-domain-containing-protein	unknown	unknown	gnl\|CDD\|366133
NZ_CP022203.1\|WP_095960190.1\|6773974_6775192_-\|cell-division-protein-FtsZ	unknown	unknown	gnl\|CDD\|236468
NZ_CP022203.1\|WP_095960193.1\|6787120_6788053_-\|UDP-N-acetylmuramate-dehydrogenase	unknown	unknown	gnl\|CDD\|237777
NZ_CP022203.1\|WP_013942040.1\|6771815_6772028_-\|biotin/lipoyl-binding-carrier-protein	unknown	unknown	gnl\|CDD\|133459
NZ_CP022203.1\|WP_095960194.1\|6791795_6793163_-\|UDP-N-acetylmuramoyl-L-alanine--D-glutamate-ligase	unknown	unknown	gnl\|CDD\|223842
NZ_CP022203.1\|WP_095960196.1\|6794360_6795761_-\|UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D--alanine-ligase	unknown	unknown	gnl\|CDD\|223841
NZ_CP022203.1\|WP_002634374.1\|6783879_6785112_-\|cell-division-protein-FtsA	unknown	unknown	gnl\|CDD\|273483
NZ_CP022203.1\|WP_095960188.1\|6772072_6773425_-\|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	unknown	unknown	gnl\|CDD\|236307
NZ_CP022203.1\|WP_095960192.1\|6785158_6786058_-\|FtsQ-type-POTRA-domain-containing-protein	unknown	unknown	gnl\|CDD\|224505
NZ_CP022203.1\|WP_002634367.1\|6770400_6770994_+\|response-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP022203.1\|WP_013942048.1\|6788058_6789477_-\|UDP-N-acetylmuramate--L-alanine-ligase	unknown	unknown	gnl\|CDD\|234757
NZ_CP022203.1\|WP_013942050.1\|6790621_6791791_-\|putative-lipid-II-flippase-FtsW	unknown	unknown	gnl\|CDD\|274232
NZ_CP022203.1\|WP_095961704.1\|6766941_6768489_-\|rhomboid-family-intramembrane-serine-protease	unknown	unknown	gnl\|CDD\|366759
NZ_CP022203.1\|WP_095960185.1\|6765253_6766252_+\|RNA-ligase-(ATP)	unknown	unknown	gnl\|CDD\|134000
NZ_CP022203.1\|WP_095960186.1\|6766307_6766850_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095960189.1\|6773562_6773952_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013942046.1\|6786167_6787124_-\|D-alanine--D-alanine-ligase	unknown	unknown	gnl\|CDD\|234948
NZ_CP022203.1\|WP_013942039.1\|6771028_6771811_-\|enoyl-CoA-hydratase/isomerase-family-protein	unknown	unknown	gnl\|CDD\|119339
NZ_CP022203.1\|WP_095960195.1\|6793182_6794361_-\|phospho-N-acetylmuramoyl-pentapeptide--transferase	unknown	unknown	gnl\|CDD\|234638
NZ_CP022203.1\|WP_043713723.1\|6789473_6790622_-\|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase	unknown	unknown	gnl\|CDD\|234825

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095960187.1\|6768603_6770325_+\|FHA-domain-containing-protein	gnl\|CDD\|366133	pfam00498, FHA, FHA domain. The FHA (Forkhead-associated) domain is a phosphopeptide binding motif.	3.34443e-17
NZ_CP022203.1\|WP_095960190.1\|6773974_6775192_-\|cell-division-protein-FtsZ	gnl\|CDD\|236468	PRK09330, PRK09330, cell division protein FtsZ; Validated.	0
NZ_CP022203.1\|WP_095960193.1\|6787120_6788053_-\|UDP-N-acetylmuramate-dehydrogenase	gnl\|CDD\|237777	PRK14652, PRK14652, UDP-N-acetylmuramate dehydrogenase.	4.16973e-158
NZ_CP022203.1\|WP_013942040.1\|6771815_6772028_-\|biotin/lipoyl-binding-carrier-protein	gnl\|CDD\|133459	cd06850, biotinyl_domain, The biotinyl-domain or biotin carboxyl carrier protein (BCCP) domain is present in all biotin-dependent enzymes, such as acetyl-CoA carboxylase, pyruvate carboxylase, propionyl-CoA carboxylase, methylcrotonyl-CoA carboxylase, geranyl-CoA carboxylase, oxaloacetate decarboxylase, methylmalonyl-CoA decarboxylase, transcarboxylase and urea amidolyase. This domain functions in transferring CO2 from one subsite to another, allowing carboxylation, decarboxylation, or transcarboxylation. During this process, biotin is covalently attached to a specific lysine.	1.04956e-22
NZ_CP022203.1\|WP_095960196.1\|6794360_6795761_-\|UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D--alanine-ligase	gnl\|CDD\|223841	COG0770, MurF, UDP-N-acetylmuramyl pentapeptide synthase [Cell envelope biogenesis, outer membrane].	7.96089e-142
NZ_CP022203.1\|WP_002634374.1\|6783879_6785112_-\|cell-division-protein-FtsA	gnl\|CDD\|273483	TIGR01174, Cell_division_protein_FtsA, cell division protein FtsA. This bacterial cell division protein interacts with FtsZ, the bacterial homolog of tubulin. It is an ATP-binding protein and shows structural similarities to actin and heat shock cognate protein 70. [Cellular processes, Cell division].	1.70887e-176
NZ_CP022203.1\|WP_095960188.1\|6772072_6773425_-\|acetyl-CoA-carboxylase-biotin-carboxylase-subunit	gnl\|CDD\|236307	PRK08591, PRK08591, acetyl-CoA carboxylase biotin carboxylase subunit; Validated.	0
NZ_CP022203.1\|WP_095960192.1\|6785158_6786058_-\|FtsQ-type-POTRA-domain-containing-protein	gnl\|CDD\|224505	COG1589, FtsQ, Cell division septal protein [Cell envelope biogenesis, outer membrane].	1.5346e-27
NZ_CP022203.1\|WP_002634367.1\|6770400_6770994_+\|response-regulator	gnl\|CDD\|225114	COG2204, AtoC, Response regulator containing CheY-like receiver, AAA-type ATPase, and DNA-binding domains [Signal transduction mechanisms].	4.81769e-35
NZ_CP022203.1\|WP_013942048.1\|6788058_6789477_-\|UDP-N-acetylmuramate--L-alanine-ligase	gnl\|CDD\|234757	PRK00421, murC, UDP-N-acetylmuramate--L-alanine ligase; Provisional.	0
NZ_CP022203.1\|WP_013942050.1\|6790621_6791791_-\|putative-lipid-II-flippase-FtsW	gnl\|CDD\|274232	TIGR02614, Putative_lipid_II_flippase_FtsW, cell division protein FtsW. This family consists of FtsW, an integral membrane protein with ten transmembrane segments. In general, it is one of two paralogs involved in peptidoglycan biosynthesis, the other being RodA, and is essential for cell division. All members of the seed alignment for this model are encoded in operons for the biosynthesis of UDP-N-acetylmuramoyl-pentapeptide, a precursor of murein (peptidoglycan). The FtsW designation is not used in endospore-forming bacterial (e.g. Bacillus subtilis), where the member of this family is designated SpoVE and three or more RodA/FtsW/SpoVE family paralogs are present. SpoVE acts in spore cortex formation and is dispensible for growth. Biological rolls for FtsW in cell division include recruitment of penicillin-binding protein 3 to the division site. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	9.3006e-144
NZ_CP022203.1\|WP_095961704.1\|6766941_6768489_-\|rhomboid-family-intramembrane-serine-protease	gnl\|CDD\|366759	pfam01694, Rhomboid, Rhomboid family. This family contains integral membrane proteins that are related to Drosophila rhomboid protein. Members of this family are found in bacteria and eukaryotes. Rhomboid promotes the cleavage of the membrane-anchored TGF-alpha-like growth factor Spitz, allowing it to activate the Drosophila EGF receptor. Analysis has shown that Rhomboid-1 is an intramembrane serine protease (EC:3.4.21.105). Parasite-encoded rhomboid enzymes are also important for invasion of host cells by Toxoplasma and the malaria parasite.	8.99467e-24
NZ_CP022203.1\|WP_095960185.1\|6765253_6766252_+\|RNA-ligase-(ATP)	gnl\|CDD\|134000	PHA02142, PHA02142, putative RNA ligase.	1.12776e-59
NZ_CP022203.1\|WP_095960194.1\|6791795_6793163_-\|UDP-N-acetylmuramoyl-L-alanine--D-glutamate-ligase	gnl\|CDD\|223842	COG0771, MurD, UDP-N-acetylmuramoylalanine-D-glutamate ligase [Cell envelope biogenesis, outer membrane].	1.84022e-150
NZ_CP022203.1\|WP_013942046.1\|6786167_6787124_-\|D-alanine--D-alanine-ligase	gnl\|CDD\|234948	PRK01372, ddl, D-alanine--D-alanine ligase; Reviewed.	4.01573e-158
NZ_CP022203.1\|WP_013942039.1\|6771028_6771811_-\|enoyl-CoA-hydratase/isomerase-family-protein	gnl\|CDD\|119339	cd06558, crotonase-like, Crotonase/Enoyl-Coenzyme A (CoA) hydratase superfamily. This superfamily contains a diverse set of enzymes including enoyl-CoA hydratase, napthoate synthase, methylmalonyl-CoA decarboxylase, 3-hydoxybutyryl-CoA dehydratase, and dienoyl-CoA isomerase. Many of these play important roles in fatty acid metabolism. In addition to a conserved structural core and the formation of trimers (or dimers of trimers), a common feature in this superfamily is the stabilization of an enolate anion intermediate derived from an acyl-CoA substrate. This is accomplished by two conserved backbone NH groups in active sites that form an oxyanion hole.	1.17824e-50
NZ_CP022203.1\|WP_095960195.1\|6793182_6794361_-\|phospho-N-acetylmuramoyl-pentapeptide--transferase	gnl\|CDD\|234638	PRK00108, mraY, phospho-N-acetylmuramoyl-pentapeptide-transferase; Provisional.	1.75412e-161
NZ_CP022203.1\|WP_043713723.1\|6789473_6790622_-\|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase	gnl\|CDD\|234825	PRK00726, murG, undecaprenyldiphospho-muramoylpentapeptide beta-N- acetylglucosaminyltransferase; Provisional.	2.10413e-163

>NZ_CP022203.1|WP_095960190.1|6773974_6775192_-|cell-division-protein-FtsZ
MDQFDQNKQAAKIRVVGAGGAGCNAVNTMILSKLDRVDFIAANTDVQALAASKAPTRLQLGQTLTKGLGAGANPEMGREAALESRDQIAAVLEGADMVFVTAGMGGGTGTGAAPIIADIAKSLGCLTVGVVTKPFLFEGNKRRKQAEQGIVELKAAVDTLITIPNQRLLSLSNEPMPLLETFKRADEVLLNAVQGISDLIQYHGYINVDFADVKTIMSDKGIALMGTGNSSGDKRALIAMQQAIASPLLEDVSIDGATGLLINITGGRDMTLQEVNEALTLVHDAADSEAEIIFGSLIDENISDEVKITIIATGFVHRDAPKVRTVVPAVQVPLSRPAPSVLANAREEVASLVPAKGNGSRPLTVESSKSVSARTAVVKDAPLPLDEDQFDIPTFLRRQGQTELP
>NZ_CP022203.1|WP_095960189.1|6773562_6773952_+|hypothetical-protein
MLPVTPPSSSSPGGVVNLHHARRAKRLDLYRGRHADRVRFVRTTLETLTQSGTLFTEEGTRRGLSLLKALQLLQRAHARLEEVSGDGVLPAARLPERVDALYTEVDGLFVRADTLSGRDEARVAQLPAR
>NZ_CP022203.1|WP_095960188.1|6772072_6773425_-|acetyl-CoA-carboxylase-biotin-carboxylase-subunit
MFQKLLIANRGEIARRIGVVARGMGLKTVAVYSDADAELPFVKEADEAVRIGPAPAKDSYLNTAAILEAAKQTGAQAVHPGYGFLSENGEFAQACKDARLIFVGPPPEAMARMKDKSQARKLVAAAGVPVVPGSDGVVPDVASAQAAAERIGFPVLIKAASGGGGIGMAVANNPAELEKAYRQCTDRAKAAFGKEGVYVERYFPAPRHIEVQILGDHHGHLIHGLERECSIQRRHQKVVEEAPSMLFAEGRNAELAQKLFSAAIAAAKAFGYANAGTVEFLYSDGEVYFIEMNARLQVEHPVTELTTGLDLIGWQLRIAAGERLTVKQEDVKRRGAALEFRIYAEDPVKFFPSPGPLKVFQPPTGEGVRLDAGYGEGNTVTPNYDPMIAKLIITGETRAQAIERSVAALQSFRIEGIKTNIPLHLRIVQDAAFQAGELDTHFLEHHAKPA
>NZ_CP022203.1|WP_013942040.1|6771815_6772028_-|biotin/lipoyl-binding-carrier-protein
MADVAAHITGTVWKIEVQVGQQINAGDTLVILESMKMEMPVEAEEGGTVKEIRVKEAQSVNEGDVLVVLG
>NZ_CP022203.1|WP_013942039.1|6771028_6771811_-|enoyl-CoA-hydratase/isomerase-family-protein
MEPVASAGASLNVEDRDDGVRVLTLSNPARRNALDDGLLARLDAALAPAPQVRALLVRGAGGAFCSGYDLTHLGPPGADGRLPDDLLVECLLKLESHPAPSVALVEGAAVGAGFDLAASCDFRVGTPNAVFLMPPARLGIVYSPEGLARAARLVGVARAKQLFLAARKLSAREALEWGLLDDCLVDAEARALALCATLAGHAPLAVSGMKESFGRLARAPLEEADRARLRDLRAAAFGSEDAKEGRAAFLEKRPPRFSGR
>NZ_CP022203.1|WP_002634367.1|6770400_6770994_+|response-regulator
MQIRILVVDDEQDNCDYLKLVLTREGYEVVTTTDPTQTVEILRGSDFHLVILDMMMPQMSGTEVLEQIRKYDTDVAVIVATAYPTVDTAVASLKAQASDYVKKPMEPEQFITAVRNALQKKGLSQDPEADLHRAIGRTIRDARKTQELTLKQLARRTGLSVSLLSQIERAESSASISSLYKIASALQLRMGELFGDT
>NZ_CP022203.1|WP_095960187.1|6768603_6770325_+|FHA-domain-containing-protein
MLKLIIEDDEGRKTVVPFVRDEITIGRQEGNTIRLTERNVSRRHARLVRLNGHVVVEDLGSYNGTRINGERIAGQSPLKEGDLVQIGDYDLALQAEGAANAAAGPITTKVPARRPEPEPEDDSDEDADDERDHTPPSQSAADARRHSTSIIRLDQVEAERPRKVVDVPAEDAPRLLVLSPDELKGQEFACIRTELRIGRTDDNDITLDHRSLSRTHAKLVREDSGEWRVIDMQSANGMTINGENYAQATLSTGDIVELGHVKLRFVNAGDAADDVADGGGSRSKLGLVAGLAALLLGGGGAAAYYMNQQGTQPAAPPVVAQVPTPVPDDAPPAAVGAQAPANNPQVAATPPPQAPETPPPPKGPSMEEQRAVADKAIAARDFDAAVEALEGIQDANGKRPRDVETRLDEARAEQLMKRRLDDVRKALGDGKLPEAEEALRESAATKAFAREYAALKVQVAEAQKKAAPPAAVPTSGTEKAPPPTQSAAAKAQAEGFEHIKGLRYRQAIEQLNKCLDLEPNRAECHLYLGSAYANDNQPEKGAVHYKRFLELAPNHAYYERVKGLVESYENPKK
>NZ_CP022203.1|WP_095961704.1|6766941_6768489_-|rhomboid-family-intramembrane-serine-protease
MGQSAGEARPGGGPWLTLILATVLVGIHGAARAAGPVGLDTLLRWGAKAGPLVVDVGQVWRLVTANLLHRDFLHLGLNVLVLLAAGTGLERLCRRRDYAALLVAAGLATMAGSLGSSGAVSVGASGIVYGCVGALLVLGRRHRAKLPARWMSGEAAVPTVLVFLWMGWTSVGVDNAGHLAGLLAGLLAGVFLEPRWRPDPGWLRPVAMVVAAVALAGAVVAERSVWRTERDDGFGISVSLPRDWRGEVDGQGRRAFSNGLPGRGRATFSAEAIEAGEPGDGSVQARQFLEEVLVLGAPGPEGRPLKVTGPVAARVGGRGAQRLSAELEGVGGATQLTALFVPRGEWVYRLVFTWPAAYPAYRGVVDRMVAELRFDEPSVLREARARALLVPGAPGPLRSLGAVLRRLGLPKEAVAPLSESVRLAPAHVQTRVELARALLEASRVEEGCHAAAEARVYGPWNTGALEAGVRCELSRGDVARALERLVEARRVDPQDARLRAAELALRTVLEASPRR
>NZ_CP022203.1|WP_095960186.1|6766307_6766850_-|hypothetical-protein
MPQIPGVKSTVSSFKPGPVVAEVADRTMNAVSLEANVAKSVGGSKSGSSEQVRTPQQVVSTIGGTSGTLNNAINVADTFETGARAIGQMSRGNVPTALPPTVVGKTLGKFVPGLNVIGAVSSLSNTRDVFTNPSSTPSQKTHAVIDSASAVVSALPVPGLSQAGAVVNTVNSLFTPSSSQ
>NZ_CP022203.1|WP_095960185.1|6765253_6766252_+|RNA-ligase-(ATP)
MERKLVSIQRIDHLEPVSGADTLLKARVMGWDVVVKKGEFAVGDACVFFEIDSLLPEGRPWAEFLRPRGFRVKTARLRGVLSQGLALPTSILPSTVPAVGTDVRDALGVVKFEPALPDTREVAGPFPGQVPKTDEVRVQSALGVLDELRGHDFFVTTKLDGTSGTFFRTLDGELVACSRNWALKRGPNPVWRMAEKYALDTVLPPGFAVQGELCGPGIQKNRLGLDALELFIFSVHDTRTGVFLGHEDFIAFCAEHGLRTVPVEHVVTGEAARAFDHGLEHYLKLAQGHYPGTKQRKEGIVVRPLVERLSPTLGGRLSFKVINNDFLLKDED
>NZ_CP022203.1|WP_002634374.1|6783879_6785112_-|cell-division-protein-FtsA
MAKQKSGEIIVGLDIGTTKICAIVGELTDSGIDIIGIGTHPSKGLRKGVVVNIEATVSSIRRAVEEAELMAGAEISHVYTGIAGGHIKGFNSQGIVAVKDKEVREADIARVIDAAKAVAIPLDREVIHVLPQEFIIDDQGGIKEPLGMAGVRLEAKVHIVTGAVSSAQNIVKCANRTGLNVSDIVLQPLASAEAVLGEDEKELGVCLVDIGGGTTDIAIFSGGSIVHTAVIALGGNNLTSDIAIGLRTPAHEAERIKQKYGCALSSLINKDDTIEVPSVGGRQPRVLGRQILCEILEPRVEEIFQLVHREIQKCGYEDLLASGVVITGGSTLLAGMPELAEEVLGLPVRRGMPRGIGGLVDVVKSPMYATGVGLVVYGARHLDRRMFRIREENVYKKVKGRMREWLEEIF
>NZ_CP022203.1|WP_095960192.1|6785158_6786058_-|FtsQ-type-POTRA-domain-containing-protein
MAPQPRTACVNPFLPMAFGKSKNRRRQDAAQQKEAVRGAVRSHGPGVLKVLGLTLGTGLLMWGGVALREWALTSPRFELEAVSFSGLQRASRVELLRLAALTKGQNLWTLDVDALERAMDQHPWLRTVEVTRRFPNRVSVEVTEHTPVAMAVLGELYVLDEEGEPFKRVTPGDGLDLPLVTGLDREGYVADPAAARERLRSALAVASAYARLSPDQAEQLSEVRLEAQSLALVTVSGQEVRLGEGDSEVKLQRLARVRRELGARGLAAEIIHLDNRARPGWVAVKISSPASERSGASMR
>NZ_CP022203.1|WP_013942046.1|6786167_6787124_-|D-alanine--D-alanine-ligase
MTPNRGAFTKDELKQKRVGVLLGGLSAERDVSLRTGEAVSGALRGLGYDVVDIDVGRDLPARLAAEKVDVAWLAVHGRYGEDGCLQGLLESLFIPYTGSGVLASALGMDKVYAKQVFVAHGIPTPAYRSFRDAASALAAADSLSFPFPVVVKPSREGSSVGVHICKTRDAYEAAVQDAAKYAGTLLVEQFVKGREVQGGVLDDEALGVIEVRAAREFYDYDAKYKAGTGTQYLFPAPLPPDQYARVNEVCLAAHQALGCSGGSRSDVIVTDGGEVFLLETNTLPGMTATSLLPKIAAGRGIDFPALCERLLLGACLKA
>NZ_CP022203.1|WP_095960193.1|6787120_6788053_-|UDP-N-acetylmuramate-dehydrogenase
MVEAGVKTALAARVESLEGCEVKAGAPLAPLTSVRAGGAAEALVRPRSPDALVALLKLAREEGVPVSILGGGANTLVGDGGVPGLTLKLPGDLFPEVADVGPEEGRLTLGAGAAIVRLVNVMRANALVGAEFLAGIPGTLGGAVAMNAGTKNGEAFRVIDAVEVATADGVGWLTKAQVPHAYRHAELPPGGVVTRVRFALRKGDVVASKAVMDADLGYRKRTQPLSQPNFGSVFTNPPGDHAGRLIELAGLKGYSLGRAQVSTLHANWIVNLGGATARDVLGLITFMQVRVLETSGVDMKPEVKRLGDFL
>NZ_CP022203.1|WP_013942048.1|6788058_6789477_-|UDP-N-acetylmuramate--L-alanine-ligase
MTRNKPPSLFKTRHAAQVHFVGLGGIGMSGIAEVLLNLGYRVSGSDLRESDITRRLARMGATFFEGHRAQNLVQADVVVISSAVRKDNPEVVAARQRKIPVIPRAEMLAELMRLKYAVAVAGSHGKTTTTSMVATVLSAAGLDPTAVVGGKVNVLDSNAKLGKSELMVVEADESDGSFLHLHPSIAIVTNIDPEHMDHYGDLETLQSAFVEFCNRVPFYGLNVLCLDNPNVQALLPRMEKRFVTYGSSHMADYRLENIQLDGFTTRFQAYRREEALGEFRVRMVGAHNAFNALAVIAVAEEMDIPLETVRESLAEFGGVQRRFTVRGEAQGITVVDDYAHHPTEVLATLAGARRAFGRRVVVAFQPHRYTRTHDLLKEFTTSFNDSDVLFVTSVYAAGEERIEGATGDALADAIRAHGHRDVTFVEKRTALPAALLPRLREGDLVLTLGAGDITHVGADLLELLRTTPLSKD
>NZ_CP022203.1|WP_043713723.1|6789473_6790622_-|undecaprenyldiphospho-muramoylpentapeptide-beta-N-acetylglucosaminyltransferase
MKVLIAGGGTGGHLFPGIALAEEVVTRHHRNEVVFVGTERGIESRVVPKEGYPLELVKVQGLKGKGFVSLLKALLALPLAFVESFRILARQKPDVVVGVGGYASGPVVLAAWLMGIPTAIQEQNALPGFTNKVLGRIVRVVFIAFEEARAFFPEKKVQLIGNPIRRKLMDNYLRSHVAHERFSVLVFGGSLGARGLNQRMTEALDSLGDLRDSLHFVHQTGKNDLDAVRKGYEDKGFQAEVVEFIDDMSSAYARADLVVCRAGATTLAELTVCKKASILIPFPHATDDHQAVNARALVEAGAALMFRESELTGEKLAQTIRELKSHPERLKGMEKKAGLLGRPEAAKELADVCVDLMVQTWGPNGRERTPVEAEKKAPRSHS
>NZ_CP022203.1|WP_013942050.1|6790621_6791791_-|putative-lipid-II-flippase-FtsW
MKTSPPSPAAALVRFDPVLLCAVLGLVSFGLVMVYSASAVLAQDKQGDSLYFLKRQLVAAGLGLGAMAVAMKVGWRRLARWAYPLLLAAIVLLVLVNIPGIGSTAGGARRWIRLPGFGLQPAEVAKFAWVVYLSYSLAKKREKVAKFSVGFVPHLALCGILVLLCMMQPDFGSSVLLVFMLFVLLFAAGAKLSYLVGMVLLALPLAYVAIASSPYRMKRILAFMDPWAHRHDVGYQVAESLMSIGSGGVSGLGLGDGRQKLFFLPEAHTDFIFSIIAEETGLIGVGILVVLYGVVLWRGVRASLAAGETFGTYLGLGISSIIAFQAAVNMCVAMGLLPTKGLTLPFVSYGGSSLVVLMGAAGVLLSLSANTQGAARPSRVGTDMREVAA
>NZ_CP022203.1|WP_095960194.1|6791795_6793163_-|UDP-N-acetylmuramoyl-L-alanine--D-glutamate-ligase
MTLALSGQKVLVFGLAKSGVAALRLLRQQGADVTALDGRSEDALGAVAHEVKSLGAALVSGPTPPGLLASRDLVVVSPGVPLALPEIQAARAAGVAVWGEVELAGRMLAGVPLFGITGTNGKSTTTALTGALFAAGDKRTFVGGNLGRPFSEAAMSPEAWDALVVELSSYQLEGIRALRPRGAAILNLTPDHIDRYPSHAAYGEAKARIFLNQQAGDFAVVNADDADVLGLARAAKAPVYGFSLTGEPVADAPALAGLAVAEPGGFRLEFLGEHYTLTNRALRGAHNAQNAMAAALLARLGGVASGAVQAGLDGYPGLPHRLESVRVLDGVEWVNDSKATNVDSVLVALRAFSSGVWLIAGGKGKGAPYAPMVEAGRGKVKGVLTMGDDADTLARAYAGAARVHACGTLAQAVARAREVAERGDTVLLSPACASFDQFKNFEDRGETFKRLVEAL
>NZ_CP022203.1|WP_095960195.1|6793182_6794361_-|phospho-N-acetylmuramoyl-pentapeptide--transferase
MLYLLYEVIQNSEAGRVLNFLRYPTFRIIAAGVFALLLGMLIGPRLIARLRLKQHGQSNVREDTPDSHQKKKGTPTMGGALILLCIAAGTLLFADLKSRAVWVMLLLTLGYGFIGFLDDWLKLSKRNSKGLAGRKKMVLQTCFFLVAVFGLLTTWTLPDGSFGPTLLINTRLTLPFIPTRWFNPDLGWFYVVFAWIVVVGTSNAVNLTDGLDGLAIVPTIVSAITFAVLCYVAGTTLSIADSETVDGVSRLVATPLYQYLGVLQVPGGAELAVFCAAIVGAGISFLWFNTYPASVFMGDIGSLALGGALGGLAMLSKNEVVSAIIHGIFFAEILSVMIQVTSFKMTGKRVFKMAPVHHHFELKGMAEPKIIVRFWIVSILCGGVALLSLKLR
>NZ_CP022203.1|WP_095960196.1|6794360_6795761_-|UDP-N-acetylmuramoyl-tripeptide--D-alanyl-D--alanine-ligase
MAASFSDEEVVQATGATRRGGPARAAYATVCTDTRALTPGCLFVALVGERFDAHAFVDAAAKGGAAGAVVARGRPLPALPEGLVLYEVEDTLRALGALGRHHRQRFRIPVCAVGGSNGKTTTKEMVGAILATRGPALKTEGNLNNEIGVPLTLFRLEPHHVAAVIEVGMNQPGEIERLARIVQPDAGVITVVQPEHLEGLGSLEGVAAAEGELFQEMGRGTTVVVNVDDALIPAQAERSTARRLTFGRAEHADVRLADVKTLGREGMVATVRHLGREWPVRLSFIGPHNAQNATAAFAVALALGYTPEECVRGLESARPYSRRLNVVDGQRGVTVIDDCYNANPASMDAALETLGTLVPANGRAVVVLGDMLELGPGELEEHARLGGQVPSHATLAAFFGPRSVKGWESASMGESAAHFTEVEPLMAWLSPRLREGDVVLVKGSRGMRLERVVAALTGTAVPGGNH

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Crispr_ID: NZ_CP022203_13

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_13

7236224-7236350

Orphan

Consensus_repeat	Method
TCATTCCACCGGGCCTCCATGGGGAGGGGCCCTC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022203_13

>merge|NZ_CP022203|13|7236224-7236350|CRISPRCasFinder
TCATTCCACCGGGCCTCCATGGGGAGGGGCCCTCCGCCTTGGCATGACCGGAGGGGGGCCGCTGCCGACCGGCCTTCTGGGTGGAGGGAACGCTCATTCCACCGGGCCTCCATGGGGAGGGGCCCTC

>NZ_CP022203|13|8|7236224-7236350|CRISPRCasFinder
TCATTCCACCGGGCCTCCATGGGGAGGGGCCCTC	CGCCTTGGCATGACCGGAGGGGGGCCGCTGCCGACCGGCCTTCTGGGTGGAGGGAACGC
TCATTCCACCGGGCCTCCATGGGGAGGGGCCCTC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_013938303.1\|7237950_7238142_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095960445.1\|7234757_7235978_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|286344
NZ_CP022203.1\|WP_095960442.1\|7227035_7227950_+\|DNA-binding-protein	unknown	unknown	gnl\|CDD\|143386
NZ_CP022203.1\|WP_095960447.1\|7237468_7237855_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|225949
NZ_CP022203.1\|WP_095960448.1\|7239356_7240190_-\|YhfC-family-intramembrane-metalloprotease	unknown	unknown	gnl\|CDD\|337619
NZ_CP022203.1\|WP_095960439.1\|7223835_7224786_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013938302.1\|7238371_7239340_+\|prolyl-aminopeptidase	unknown	unknown	gnl\|CDD\|130316
NZ_CP022203.1\|WP_095960446.1\|7236953_7237439_-\|transposase	unknown	unknown	gnl\|CDD\|315923
NZ_CP022203.1\|WP_013938305.1\|7233624_7234632_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|226952
NZ_CP022203.1\|WP_095960438.1\|7223341_7223737_+\|RidA-family-protein	unknown	unknown	gnl\|CDD\|100011
NZ_CP022203.1\|WP_095960450.1\|7242185_7243199_+\|TIGR02266-family-protein	unknown	unknown	gnl\|CDD\|274060
NZ_CP022203.1\|WP_095960449.1\|7240263_7241670_-\|M20/M25/M40-family-metallo-hydrolase	unknown	unknown	gnl\|CDD\|236127
NZ_CP022203.1\|WP_011555961.1\|7241746_7242121_+\|response-regulator	unknown	unknown	gnl\|CDD\|381097
NZ_CP022203.1\|WP_095960452.1\|7245043_7246081_-\|oxidoreductase	unknown	unknown	gnl\|CDD\|99810
NZ_CP022203.1\|WP_095960444.1\|7232824_7233628_-\|ABC-2-family-transporter-protein	unknown	unknown	gnl\|CDD\|226953
NZ_CP022203.1\|WP_013938307.1\|7232016_7232823_-\|ABC-2-family-transporter-protein	unknown	unknown	gnl\|CDD\|226218
NZ_CP022203.1\|WP_095960443.1\|7227901_7229077_-\|acetyltransferase	unknown	unknown	gnl\|CDD\|224001
NZ_CP022203.1\|WP_095960451.1\|7243437_7245066_+\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP022203.1\|WP_095960440.1\|7224831_7225527_+\|response-regulator-transcription-factor	unknown	unknown	gnl\|CDD\|223816
NZ_CP022203.1\|WP_095960441.1\|7225523_7226918_+\|HAMP-domain-containing-histidine-kinase	unknown	unknown	gnl\|CDD\|223715

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095960445.1\|7234757_7235978_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|286344	pfam09243, Rsm22, Mitochondrial small ribosomal subunit Rsm22. Rsm22 has been identified as a mitochondrial small ribosomal subunit and is a methyltransferase. In Schizosaccharomyces pombe, Rsm22 is tandemly fused to Cox11 (a factor required for copper insertion into cytochrome oxidase) and the two proteins are proteolytically cleaved after import into the mitochondria.	2.36236e-23
NZ_CP022203.1\|WP_095960442.1\|7227035_7227950_+\|DNA-binding-protein	gnl\|CDD\|143386	cd00141, NT_POLXc, Nucleotidyltransferase (NT) domain of family X DNA Polymerases. X family polymerases fill in short gaps during DNA repair. They are relatively inaccurate enzymes and play roles in base excision repair, in non-homologous end joining (NHEJ) which acts mainly to repair damage due to ionizing radiation, and in V(D)J recombination. This family includes eukaryotic Pol beta, Pol lambda, Pol mu, and terminal deoxyribonucleotidyl transferase (TdT). Pol beta and Pol lambda are primarily DNA template-dependent polymerases. TdT is a DNA template-independent polymerase. Pol mu has both template dependent and template independent activities. This subgroup belongs to the Pol beta-like NT superfamily. In the majority of enzymes in this superfamily, two carboxylates, Dx[D/E], together with a third more distal carboxylate, coordinate two divalent metal cations involved in a two-metal ion mechanism of nucleotide addition. These three carboxylate residues are fairly well conserved in this family.	8.20837e-27
NZ_CP022203.1\|WP_095960447.1\|7237468_7237855_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|225949	COG3415, COG3415, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	1.62699e-14
NZ_CP022203.1\|WP_095960448.1\|7239356_7240190_-\|YhfC-family-intramembrane-metalloprotease	gnl\|CDD\|337619	pfam10086, DUF2324, Putative membrane peptidase family (DUF2324). This domain, found in various hypothetical bacterial proteins, has no known function. This family appears to be related to the prenyl protease 2 family pfam02517, suggesting this family may be peptidases.	1.16189e-57
NZ_CP022203.1\|WP_095960452.1\|7245043_7246081_-\|oxidoreductase	gnl\|CDD\|99810	cd06214, PA_degradation_oxidoreductase_like, NAD(P) binding domain of ferredoxin reductase like phenylacetic acid (PA) degradation oxidoreductase. PA oxidoreductases of E. coli hydroxylate PA-CoA in the second step of PA degradation. Members of this group typically fuse a ferredoxin reductase-like domain with an iron-sulfur binding cluster domain. Ferredoxins catalyze electron transfer between an NAD(P)-binding domain of the alpha/beta class and a discrete (usually N-terminal) domain which vary in orientation with respect to the NAD(P) binding domain. The N-terminal portion may contain a flavin prosthetic group, as in flavoenzymes, or use flavin as a substrate. Ferredoxin-NADP+ (oxido)reductase is an FAD-containing enzyme that catalyzes the reversible electron transfer between NADP(H) and electron carrier proteins such as ferredoxin and flavodoxin. Isoforms of these flavoproteins (i.e. having a non-covalently bound FAD as a prosthetic group) are present in chloroplasts, mitochondria, and bacteria and participate in a wide variety of redox metabolic pathways. The C-terminal domain contains most of the NADP(H) binding residues and the N-terminal domain interacts non-covalently with the isoalloxazine rings of the flavin molecule which lies largely in a large gap betweed the two domains. Ferredoxin-NADP+ reductase first accepts one electron from reduced ferredoxin to form a flavin semiquinone intermediate. The enzyme then accepts a second electron to form FADH2 which then transfers two electrons and a proton to NADP+ to form NADPH.	4.65737e-61
NZ_CP022203.1\|WP_013938302.1\|7238371_7239340_+\|prolyl-aminopeptidase	gnl\|CDD\|130316	TIGR01249, Putative_proline_iminopeptidase, proline iminopeptidase, Neisseria-type subfamily. This model represents one of two related families of proline iminopeptidase in the alpha/beta fold hydrolase family. The fine specificities of the various members, including both the range of short peptides from which proline can be removed and whether other amino acids such as alanine can be also removed, may vary among members.	7.99775e-166
NZ_CP022203.1\|WP_095960446.1\|7236953_7237439_-\|transposase	gnl\|CDD\|315923	pfam13358, DDE_3, DDE superfamily endonuclease. This family of proteins are related to pfam00665 and are probably endonucleases of the DDE superfamily. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain 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.	5.85333e-31
NZ_CP022203.1\|WP_013938305.1\|7233624_7234632_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|226952	COG4586, COG4586, ABC-type uncharacterized transport system, ATPase component [General function prediction only].	1.53325e-127
NZ_CP022203.1\|WP_095960438.1\|7223341_7223737_+\|RidA-family-protein	gnl\|CDD\|100011	cd06154, YjgF_YER057c_UK114_like_6, This group of proteins belong to a large family of YjgF/YER057c/UK114-like proteins present in bacteria, archaea, and eukaryotes with no definitive function. The conserved domain is similar in structure to chorismate mutase but there is no sequence similarity and no functional connection. Members of this family have been implicated in isoleucine (Yeo7, Ibm1, aldR) and purine (YjgF) biosynthesis, as well as threonine anaerobic degradation (tdcF) and mitochondrial DNA maintenance (Ibm1). This domain homotrimerizes forming a distinct intersubunit cavity that may serve as a small molecule binding site.	1.33899e-59
NZ_CP022203.1\|WP_095960450.1\|7242185_7243199_+\|TIGR02266-family-protein	gnl\|CDD\|274060	TIGR02266, gmx_TIGR02266, Myxococcus xanthus paralogous domain TIGR02266. This domain is related to Type IV pilus assembly protein PilZ (pfam07238). It is found in at least 12 copies in Myxococcus xanthus DK 1622.	6.82734e-28
NZ_CP022203.1\|WP_095960449.1\|7240263_7241670_-\|M20/M25/M40-family-metallo-hydrolase	gnl\|CDD\|236127	PRK07907, PRK07907, hypothetical protein; Provisional.	1.79987e-152
NZ_CP022203.1\|WP_011555961.1\|7241746_7242121_+\|response-regulator	gnl\|CDD\|381097	cd17542, REC_CheY, phosphoacceptor receiver (REC) domain of chemotaxis protein CheY. The chemotaxis response regulator CheY contains a stand-alone REC domain. Chemotaxis is a behavior known for motile bacteria that directs their movement in response to chemical gradients. CheY is involved in transmitting sensory signals from chemoreceptors to the flagellar motors. Phosphorylated CheY interacts with the flagella switch components FliM and FliY, which causes counterclockwise rotation of the flagella, resulting in smooth swimming. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	2.8604e-26
NZ_CP022203.1\|WP_095960444.1\|7232824_7233628_-\|ABC-2-family-transporter-protein	gnl\|CDD\|226953	COG4587, COG4587, ABC-type uncharacterized transport system, permease component [General function prediction only].	1.60217e-40
NZ_CP022203.1\|WP_013938307.1\|7232016_7232823_-\|ABC-2-family-transporter-protein	gnl\|CDD\|226218	COG3694, COG3694, ABC-type uncharacterized transport system, permease component [General function prediction only].	2.12822e-56
NZ_CP022203.1\|WP_095960443.1\|7227901_7229077_-\|acetyltransferase	gnl\|CDD\|224001	COG1075, LipA, Predicted acetyltransferases and hydrolases with the alpha/beta hydrolase fold [General function prediction only].	5.39275e-11
NZ_CP022203.1\|WP_095960451.1\|7243437_7245066_+\|GAF-domain-containing-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	2.79109e-45
NZ_CP022203.1\|WP_095960440.1\|7224831_7225527_+\|response-regulator-transcription-factor	gnl\|CDD\|223816	COG0745, OmpR, Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain [Signal transduction mechanisms / Transcription].	3.49841e-71
NZ_CP022203.1\|WP_095960441.1\|7225523_7226918_+\|HAMP-domain-containing-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.43519e-36

>NZ_CP022203.1|WP_095960445.1|7234757_7235978_+|methyltransferase-domain-containing-protein
MSNAYSKDLERWMPRLIAVWRASRGRGGAGGPETRLTPQEVKEVAAGVRQLSLGLTRERQLAGARYMDDPKLLGAYLLFYWPVSYAQARQVLGELPSRPRQVLDLGSGPGPVAFAALDAGGGQVTAADRSKPALTLARNLAAEAGEALATRDWDPTKKGAALPEGQFDLITMGHVVNELYGAGDAAIAPRAALLETILAKVKRGGSLLVMEPALRETSRGLLQVRDAMVARGYAIRAPCMYRGPCPALVKETDWCHAERAWPMPRVVEELARAASLHKESLKMSYLVLAPKDEAWPELTPGRLFRIVSEPLEGKGRHRYIGCGPEGRVGLAMQERHRNERNERFLKLNRGDVISVTETEPKGDGLALDERTEVRMVAPAGKQVPPPPPKEDAPSGPGAGPRPGAPS
>NZ_CP022203.1|WP_013938305.1|7233624_7234632_-|ATP-binding-cassette-domain-containing-protein
MISVRGLRKHYKVHKRPPGLKAALRSLVHRSYTTVKAVDGISFDIRPGERVGFLGPNGAGKTTTLKVLSGLLYPSDGEVTVDGHVPQKREEAFLKKIMLVMGQKQQLLWDLPPAETFELNRAIYDVPQAQYKKTMSDLVELLEIGDLIGKPTRQLSLGERMKCELAAALIHQPRVLFLDEPTIGLDVAMQATMRTFIKEYNEKYGATLILTSHYMDDVAALCPRVIVIDKGLLSYDGGLDALVQRVRPEKRVVLRLSEEVDAARLAPLGKVVTHEPGSAVLQVQQEAVNATITRALSTLPVMDLTVENAPLEEVMSELFAESKARRAAAPEPVPA
>NZ_CP022203.1|WP_095960444.1|7232824_7233628_-|ABC-2-family-transporter-protein
MSARTVLRAFPTLLRVGFAEAVAYRAEMLIWVLSTTMPLVNMVLWMAVSREAPVGRFGEADFISYFLATFAVRQLATSWAAWLINWEVKQGTLAMRLLRPISPLWTYAVESIAAFPMRLLVAVPVVLLSVALVGEKAVPQHAWQWGFFVLSVIGGWAVAFLANVAIGALCFFLESSQKVLEVWLVLFFVCSGYMYPVELLPPTLRAIIDWLPFRYQIGVPVEMLTGAYGWQESLRLLAAQWAWVAVLGGLAAVTWKQGVRRFAAFGG
>NZ_CP022203.1|WP_013938307.1|7232016_7232823_-|ABC-2-family-transporter-protein
MNLKRYLRLLGIQLKASGLLSLQYRADFFTEGLTSLFWTFTALAPLFVVYGERPNIEGWSFGEALLVVGWFTLLQGILEGAINPSLTGVVEHIRKGTLDFVLLKPADAQFLVSTQRFQPWRAFNVLTGVGLFVYAFTHLGRWPSVTGLLASVLLLGTSTLLLYSLWILTVSAAFFVVRVDNLTYLFTSIFDFARWPSSVFQGVGRGALTMVFTYVIPLALMTTFPAQAMLGRLPFQSLLGAVAGAGIFAWGSRQVWLRSIRRYTSASS
>NZ_CP022203.1|WP_095960443.1|7227901_7229077_-|acetyltransferase
MKGLQAVVMAGVFVGVLGLAPAAWAGAAKTRYPVVFAHGMGGFDDLLGFDYWGNDYGTFVGKACASSLDTDCNGDLARGQRAFVAQVAAFQSSEVRGLDLADDIEGFMATTGAAKVSIIGHSQGGIDARKAARVLRERRGVTSVAVLASVSSPHRGSPVARYILDLKPGVTSVVAALARYYGDSVYAPGNDAYAAAKQLVYDDYAASDGVVTGMKVFNEKYPVSSLYAGRYVSLITAQHGVNVNPALYLLKEFLFDIDGDGHCEGDGDNDGAAGCGDGVHDEADDDGMVGISSQQMGRRLRYHDAFFGFDSVTEDTSIPVLSGLNAPSRLQSTSMSSVVSQDHVDVVGVGPDTFDEPEFYAALIHYIATQEGGLAAQAPGGGASTSSDSTP
>NZ_CP022203.1|WP_095960442.1|7227035_7227950_+|DNA-binding-protein
MEAAMGVAWKDNIDVADALERVADLLEEQDAMPFRVGAYRKAADTIAQWPQPVAELLAEKDEAGLRELPGVGKSIAAAMAELIRTGHLSLLQRLETEHSPEQLLASVPGIGAELARRIHDELGVRSLEELEQAAHDGRLERVEGFGPRRGEQVRELLGARLGRERRGAARRSEAHDEGPRPDVGLILQVDEEYRRRADAGELRRIAPRRFNPSGEAWLPVLRRKLAGWNFRVLFSNTALAHQQGTTRDWVVLYFDQEGDEGQCTVVTAHGGPLDGRRVVRGREVECLAYYGVESEEVEAPPPGA
>NZ_CP022203.1|WP_095960441.1|7225523_7226918_+|HAMP-domain-containing-histidine-kinase
MRLRNRLAQRILVASALLGLLGTLAASILAVFLAVDAALKHGARMTAALVLAPQTADCRTTPGWRFRSPDGVEVEAFDLAQVGTGTPGARPDPTLLARLAQGEREPTVFYPPLFHPEAEWAGATLLKLGEAGPCSLLELRWPLMHERALVGQWVFASAVLFTLLAAALSTFAVAQPLLQRLRGLHRAAGMLGATGYRSAADGQDDELGELSRVLDATHARVQEDATRIEAQKHALERHLADVAHDLKTPIASLQLSLELASTTPTEPAAALLRQGLEDTVYLTSLVDNLHLACQLGEGIDPTAGDPRVELGQTMERVVRRLQQLARLLERTVECARPDEALWVRCNPTMLEQALSNLLHNAVTHGEAGGHVVAVLEDAEPGRFRLTVLDDGPGLPPGDLERLGERGFRAQATRRRATRGSGLGLSIVRELCHRVGFSLAFAPNVPTGLKVVIEGPRASDERVPR
>NZ_CP022203.1|WP_095960440.1|7224831_7225527_+|response-regulator-transcription-factor
MSMNPSARILVVEDDAPIAAGIVRGLKLAGFQVALATDGVLALEMAEREQPDLVVLDLNLPGQDGFEVMEAWRFRLRVPIIVLTARQELEARLRSFGLGAADYLPKPFWMEELVARIRARLLLQEERPRRVLRWDDVSLDLDAREASREGTGVLPLTRHEFDVLAYLVERPGRALTRAQIAQHALPPSEERDDRTVDSHVARIRKKLGPAGARIQTSWGIGYRFVPDEAPR
>NZ_CP022203.1|WP_095960439.1|7223835_7224786_+|hypothetical-protein
MSLSKSFKKAVKKVKKSAKKAGNAVVDTANKAADTVTDTAGTVTNQVSREAEQLAREVDTLTRDAAKLAEQAYAESLAAGEAAWNEVVELSTRFLTDALSDVAQTLAEDVYREHLALLEGMAETGYALLTNPTRHKQVEFLVGQSSQKKKDDDTQKTVSSLSQDASVQRTNNDARGKGFITFSLGSGGDAAYGAGAEGNFGFAFDLPELKELRGYYGVGGVAGLATGASLDFQLGVWADKPSKLDGPELSVSLGASLKYGGSVQVVFNAPATEREWTDFLTSGKLELAGLVVSLGVGVSPTPEVSATVGCGYTWVY
>NZ_CP022203.1|WP_095960438.1|7223341_7223737_+|RidA-family-protein
MKRTQHSTGTPWEPKVGYSRAVRVGPFVSVSGTTATDGHGNIVGVGDAYIQARRALQNIQAALEALGARLEDVVRTRMYVTDIQRWEEVGRAHGEFFAHIRPATSMVEVSRLISPEILVEIEADAVVTDAG
>NZ_CP022203.1|WP_095960446.1|7236953_7237439_-|transposase
MRKGAPDKLVVVDEMGSRTDMTRTHGRAPAGERLTGEAVPRNRGCVTTVLGALTHQGIEAHMEVEGGTSLEVWDNLAAHKCRALIDVIESRGARVVFLPPYSPDFSPIELAWSKVKARLRKWRFRTRSALRQGIHLALAAISPSDAAGWFAHCGYSVAQAI
>NZ_CP022203.1|WP_095960447.1|7237468_7237855_-|helix-turn-helix-domain-containing-protein
MSSTHSLDLRERVIAAWQEGEGKSAIARRFMLGYAPVRRYIARFETTGSVRARPHGGGAPRKVDAAGEEVLRRLVCERPDATDEELARVYAVRAGCAINHTTVNRALRRMGLTRKKDPSTRPSATPRQ
>NZ_CP022203.1|WP_013938303.1|7237950_7238142_-|hypothetical-protein
MNIASLIRPVTVPLQARAPRRLKLVRVQATVLAQGTVGAMKDGVKAFRHMCDVLTGGYSQVRH
>NZ_CP022203.1|WP_013938302.1|7238371_7239340_+|prolyl-aminopeptidase
MSVPPRPLRSLYPPLEPYRAGRLRVSGGHEVYFEESGNPEGKPVLFVHGGPGGGTDPRQRRFFDPAAYRIILFDQRGCGRSTPHASLEENTTWDLVADMERLREHLGVPHWQLFGGSWGSTLSLAYAQTHPERVTELVLRGIFLLRKQEIDWFYQRGASALFPDAWEYYLEPIPPEERGDLLTAYHRRLMGPDVKAQQEAARAWSVWEGRTSCLYPNAELVARNSGDAFALAFARIECHYFVNRGFLRSDTQLLDDVHRIRHIPAVIVQGRYDVVCPPESAWALHKAWPEAEFVMVADAGHSANEPGNTSALVEATDRFRGR
>NZ_CP022203.1|WP_095960448.1|7239356_7240190_-|YhfC-family-intramembrane-metalloprotease
MDAVDTRLVASYAVAIAFDVLMPVGVVLWARRRLGASWKVVGWGAAAFALSQLLTRLPMVQVAQYFMRDALKASSVLLGAWIAVLSLTAGLFEETARLWAFRKPLKDFRRWRDAVGFGAGHGGLESALLVGGLAVLGLVNVIVLSALDPSTLSLKPEQAAQVVEAKATIAALDWWMPLLGAYERLGAMAVHIALSVVVLQRFLRGEVRWYWFAVAAHASFNALTVVVGKLATAAWGTRFGALAGEGMVTVAALLSVWVIVYFRRVEAARESVAPGLT
>NZ_CP022203.1|WP_095960449.1|7240263_7241670_-|M20/M25/M40-family-metallo-hydrolase
MSMSTDNALSHFESRKQTYLEDLKSLVRIPSVSFPGFDATQVRRSAEATARLLKDRGFENVQLLEIEGTHPYVYGEVLKAPGRPTLLLYAHHDVQPAGDEAAWKSPPFEPVERDGRLYGRGSADDKAGIVVHTSAVESWLKGAGQLPLNVKVIIEGEEEIGSNFLGAFLQKHAALLKADAIVLTDTSNFDTGLPSITTALRGLVTVDVEVRALRQAVHSGMWGGPVPDPVMALCRMLATLTHADGSIAIEGLRERVKPLTEGERQSIQALPGDEAHFRAQSGLLPGAQVLGGGTHPWEMNWRQPSIAINAIQASSRKDARNIICDSAWARVGIRIVPDLEASDVEQRLKAHLREVCPWGLEVHFDTEGASGWWYTDPSHPAFQAAFRALEKGYGTKAVAIGCGASIPFVEPFAKELGGVPALLIGVEDPYTYAHSENESLHLGDWEKSIRSAIHLYAELAEALSASRA
>NZ_CP022203.1|WP_011555961.1|7241746_7242121_+|response-regulator
MSDTPTLLLVDDDSFVRRILKDVIADTGIELRLLEAADGEEGLAVAAREKPAVMFLDLFMPKKSGLEVLGAIKAVSPTTRVLVISSMDAEPVVEQAMAAGAVGFVGKPFHPLEIASAVRQALAH
>NZ_CP022203.1|WP_095960450.1|7242185_7243199_+|TIGR02266-family-protein
MLGPLALQALRELIASGRLKAAVRASRDGTNWVALPELPELRDLFASARPTPSVEQQQAERLRAQMRAMQSLPAHEVFGLKPTANLDELRLAYFRMAKRFTPDHLAPDTHPELKKVSAEIFDFLSRRMRDAEATWTQAAQAPRPPPPVVAAAPRPVVPAPPRPPPVVHAAPAAVAPAPPPRPVQAAPVMARAPIAPPPPAPPPPAPSTRRAAAAPTYSSAEFVGLERRSDDRIHADVKVTLQTAGIFTDHRIINLSSGGLFIATDKPLRLGTLVELTLRFDEPPRVLTLRSSVIWENSLEDGKNPRGYGLRLSHLRPEEKEFVQKYLARAKELKKKP
>NZ_CP022203.1|WP_095960451.1|7243437_7245066_+|GAF-domain-containing-protein
MTAVTTASAADRLLEAMPLPTAILRGEQVLRVNTALATLLGVPAAELEALPLSESIRRFVPEERGWVEPMYQTLSQGGPIPERPVWVRVQPAHGPQRTLSVWHAPGAHADELVVVLLEAEAEDSVRRLTEALVVAASTMLRCRDERSVLETAVEAIYRQGFSVSIMRVEGDAFRYGPARQSPFNVADAEAVYGMPLDAVRIPRPALPHLLEVLERRKAVFHHDMLGVARYPDAPDGVAPVHQLHPPDTRGLDAPVLVEGQPYGVLCVQGPALTPAGASTLELFAQLVGGALENVRHHQTSAVRLEEVSRLQDELVARERLEVLGEAAGVVAHEVRNPLGAILNAVAVLRREAHLGPTGQAAVGMLEEEAIRLEDIVRDLLDVVRPLEPRPRPVQLGELVRRALGQMHGPPDAPTLRFSVDEAAGTPALEGDETLLQLAVTHLVRNAVQASPAGGKVRMTVEPADGGVRLVVEDEGPGIPDVDPQRVFQPFFLTRANGRGLGLAIVRRVVLAHEGSVRASSRPRGGARFELWLPLVPSRMSPV
>NZ_CP022203.1|WP_095960452.1|7245043_7246081_-|oxidoreductase
MSRVSTSPVLAPRLPGRPSYSQRSCGTGGRDGFCFPSSHPPHGLAMGGRMSLVEVRASRARKPVEYEVTVDHVRMDTHDTATLFLDFGGVPLDYKAGQFLNIDPHQFPALARLSAYLQEQKGRKEPQRSYSLASAPHEPLVAITVKDEEFIPGLTRYPPLLSPYLVHGRLTGARLKVMAFMGPYVLPEDVEARTGHIVHLVAGSGAVPNFAILKDALHRGLKLRHTFLFSNKTWGDVLYGDELAALARAHPDRVRVVHTLTRETDESRFGADVRKGRVHQALLEELIQDRDTCLVYACGPAITPWDRRKALETRTPSTPRFMETVLGHLHALGIDDKRIKRETYG

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Crispr_ID: NZ_CP022203_14

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_14

8150132-8150250

Orphan

Consensus_repeat	Method
GCGTGAGCGCGCGCCCCGGAGCGAGGGCTGCCGCGGTGCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022203_14

>merge|NZ_CP022203|14|8150132-8150250|CRISPRCasFinder
GCGTGAGCGCGCGCCCCGGAGCGAGGGCTGCCGCGGTGCTACATGACTCTGGGATTCACTGGCGCGGGTGGATGGCTCAGCGTGAGCGCACGCCCCGGAGCGAGGGCTGCCGCGGTGCT

>NZ_CP022203|14|9|8150132-8150250|CRISPRCasFinder
GCGTGAGCGCGCGCCCCGGAGCGAGGGCTGCCGCGGTGCT	ACATGACTCTGGGATTCACTGGCGCGGGTGGATGGCTCA
GCGTGAGCGCACGCCCCGGAGCGAGGGCTGCCGCGGTGCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095960948.1\|8144855_8146121_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369943
NZ_CP022203.1\|WP_095960954.1\|8159058_8160978_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP022203.1\|WP_095960945.1\|8138936_8141534_-\|TonB-family-protein	unknown	unknown	gnl\|CDD\|238657
NZ_CP022203.1\|WP_043712729.1\|8152953_8153175_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013937513.1\|8143990_8144368_-\|thioredoxin	unknown	unknown	gnl\|CDD\|239245
NZ_CP022203.1\|WP_013937517.1\|8138100_8138940_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013937502.1\|8155159_8155648_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP022203.1\|WP_013937501.1\|8155770_8156508_-\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|376576
NZ_CP022203.1\|WP_013937509.1\|8148191_8148848_-\|LON-peptidase-substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|366967
NZ_CP022203.1\|WP_043710096.1\|8144381_8144705_-\|FKBP-type-peptidyl-prolyl-cis-trans-isomerase	unknown	unknown	gnl\|CDD\|223619
NZ_CP022203.1\|WP_095960946.1\|8141642_8142554_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095960952.1\|8153800_8154460_-\|HAD-family-hydrolase	unknown	unknown	gnl\|CDD\|223620
NZ_CP022203.1\|WP_095960944.1\|8136845_8138093_+\|sterol-desaturase-family-protein	unknown	unknown	gnl\|CDD\|225546
NZ_CP022203.1\|WP_013937500.1\|8156833_8157712_+\|general-secretion-pathway-protein-GspE	unknown	unknown	gnl\|CDD\|274186
NZ_CP022203.1\|WP_095960951.1\|8153188_8153776_-\|putative-glycolipid-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|377662
NZ_CP022203.1\|WP_095960949.1\|8146217_8148110_-\|NAD(+)-synthase	unknown	unknown	gnl\|CDD\|237577
NZ_CP022203.1\|WP_095960947.1\|8142561_8143797_-\|hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl\|CDD\|223715
NZ_CP022203.1\|WP_095960953.1\|8157939_8159049_+\|bifunctional-methionine-sulfoxide-reductase-B/A-protein	unknown	unknown	gnl\|CDD\|235499
NZ_CP022203.1\|WP_013937503.1\|8154549_8155134_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP022203.1\|WP_095960950.1\|8150304_8152836_-\|MASE1-domain-containing-protein	unknown	unknown	gnl\|CDD\|283013

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095960948.1\|8144855_8146121_-\|hypothetical-protein	gnl\|CDD\|369943	pfam08549, SWI-SNF_Ssr4, Fungal domain of unknown function (DUF1750). This is a fungal domain of unknown function.	2.15645e-05
NZ_CP022203.1\|WP_095960954.1\|8159058_8160978_-\|PAS-domain-S-box-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	2.54083e-78
NZ_CP022203.1\|WP_095960945.1\|8138936_8141534_-\|TonB-family-protein	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.	5.83427e-18
NZ_CP022203.1\|WP_013937513.1\|8143990_8144368_-\|thioredoxin	gnl\|CDD\|239245	cd02947, TRX_family, TRX family; composed of two groups: Group I, which includes proteins that exclusively encode a TRX domain; and Group II, which are composed of fusion proteins of TRX and additional domains. Group I TRX is a small ancient protein that alter the redox state of target proteins via the reversible oxidation of an active site dithiol, present in a CXXC motif, partially exposed at the protein's surface. TRX reduces protein disulfide bonds, resulting in a disulfide bond at its active site. Oxidized TRX is converted to the active form by TRX reductase, using reducing equivalents derived from either NADPH or ferredoxins. By altering their redox state, TRX regulates the functions of at least 30 target proteins, some of which are enzymes and transcription factors. It also plays an important role in the defense against oxidative stress by directly reducing hydrogen peroxide and certain radicals, and by serving as a reductant for peroxiredoxins. At least two major types of functional TRXs have been reported in most organisms; in eukaryotes, they are located in the cytoplasm and the mitochondria. Higher plants contain more types (at least 20 TRX genes have been detected in the genome of Arabidopsis thaliana), two of which (types f amd m) are located in the same compartment, the chloroplast. Also included in the alignment are TRX-like domains which show sequence homology to TRX but do not contain the redox active CXXC motif. Group II proteins, in addition to either a redox active TRX or a TRX-like domain, also contain additional domains, which may or may not possess homology to known proteins.	1.03122e-36
NZ_CP022203.1\|WP_013937502.1\|8155159_8155648_-\|biopolymer-transporter-ExbD	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	1.79226e-16
NZ_CP022203.1\|WP_095960944.1\|8136845_8138093_+\|sterol-desaturase-family-protein	gnl\|CDD\|225546	COG3000, ERG3, Sterol desaturase [Lipid metabolism].	1.61188e-29
NZ_CP022203.1\|WP_013937501.1\|8155770_8156508_-\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|376576	pfam01618, MotA_ExbB, MotA/TolQ/ExbB proton channel family. This family groups together integral membrane proteins that appear to be involved translocation of proteins across a membrane. These proteins are probably proton channels. MotA is an essential component of the flageller motor that uses a proton gradient to generate rotational motion in the flageller. ExbB is part of the TonB-dependent transduction complex. The TonB complex uses the proton gradient across the inner bacterial membrane to transport large molecules across the outer bacterial membrane.	3.94646e-23
NZ_CP022203.1\|WP_013937509.1\|8148191_8148848_-\|LON-peptidase-substrate-binding-domain-containing-protein	gnl\|CDD\|366967	pfam02190, LON_substr_bdg, ATP-dependent protease La (LON) substrate-binding domain. This domain has been shown to be part of the PUA superfamily. This domain represents a general protein and polypeptide interaction domain for the ATP-dependent serine peptidase, LON, Peptidase_S16, pfam05362. ATP-dependent Lon proteases are conserved in all living organisms and catalyze rapid turnover of short-lived regulatory proteins and many damaged or denatured proteins.	2.0712e-27
NZ_CP022203.1\|WP_043710096.1\|8144381_8144705_-\|FKBP-type-peptidyl-prolyl-cis-trans-isomerase	gnl\|CDD\|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	4.4775e-53
NZ_CP022203.1\|WP_095960952.1\|8153800_8154460_-\|HAD-family-hydrolase	gnl\|CDD\|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	2.5137e-52
NZ_CP022203.1\|WP_095960951.1\|8153188_8153776_-\|putative-glycolipid-binding-domain-containing-protein	gnl\|CDD\|377662	pfam06475, Glycolipid_bind, Putative glycolipid-binding. This family has a novel fold known as a spiral beta-roll, consisting of a 15-stranded beta sheet wrapped around a single alpha helix. It forms dimers. It has some structural similarity to the E. coli lipoprotein localization factors LolA and LolB. Its structure suggests that it may have a role in glycolipid binding. Its genomic context supports a role in glycolipid metabolism.	1.12646e-56
NZ_CP022203.1\|WP_013937500.1\|8156833_8157712_+\|general-secretion-pathway-protein-GspE	gnl\|CDD\|274186	TIGR02538, Type_IV_pilus_assembly_protein_PilF, type IV-A pilus assembly ATPase PilB. This model describes a protein of type IV pilus biogenesis designated PilB in Pseudomonas aeruginosa but PilF in Neisseria gonorrhoeae; the more common usage, reflected here, is PilB. This protein is an ATPase involved in protein export for pilin assembly and is closely related to GspE (TIGR02533) of type II secretion, also called the main terminal branch of the general secretion pathway. Note that type IV pilus systems are often divided into type IV-A and IV-B, with the latter group including bundle-forming pilus, mannose-sensitive hemagglutinin, etc. Members of this family are found in type IV-A systems. [Cell envelope, Surface structures, Protein fate, Protein and peptide secretion and trafficking].	1.71469e-19
NZ_CP022203.1\|WP_095960949.1\|8146217_8148110_-\|NAD(+)-synthase	gnl\|CDD\|237577	PRK13981, PRK13981, NAD synthetase; Provisional.	5.46947e-107
NZ_CP022203.1\|WP_095960947.1\|8142561_8143797_-\|hybrid-sensor-histidine-kinase/response-regulator	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.5955e-44
NZ_CP022203.1\|WP_095960953.1\|8157939_8159049_+\|bifunctional-methionine-sulfoxide-reductase-B/A-protein	gnl\|CDD\|235499	PRK05550, PRK05550, bifunctional methionine sulfoxide reductase B/A protein; Provisional.	9.96208e-161
NZ_CP022203.1\|WP_013937503.1\|8154549_8155134_-\|biopolymer-transporter-ExbD	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	1.61423e-13
NZ_CP022203.1\|WP_095960950.1\|8150304_8152836_-\|MASE1-domain-containing-protein	gnl\|CDD\|283013	pfam05231, MASE1, MASE1. Predicted integral membrane sensory domain found in histidine kinases, diguanylate cyclases and other bacterial signaling proteins. This entry also includes members of the 8 transmembrane UhpB type (8TMR-UT) domain family.	5.0014e-49

>NZ_CP022203.1|WP_013937509.1|8148191_8148848_-|LON-peptidase-substrate-binding-domain-containing-protein
MTAQERIERAASALKVFPLPSAVLFPHTVIPLHIFEPRYRALVRDALAGDRVLALSQLEPGWEGNYGGKPPMLPMMCAGVIVWDEQVEEGRYNILLQGVSRVRMTSELTTEKAYREVLAEALPDVPYEGPEEEQLRQAVFELAGRVPPSFAENLLPVAARAQGGMLADVVASAVIPEPERRQALLAELDVRKRLEGVLEDVGALIGRLQPLRPTGPLN
>NZ_CP022203.1|WP_095960949.1|8146217_8148110_-|NAD(+)-synthase
MRLVKLGLASVNTTVGAFTRNTDRALALAGKMAAEGVTLGVFQEQVIAGYPAEDMVQWQGFMDRQWPELERFARETASLSTVFVVGVGVAHQGLRLNCAAVVAGGRILGLVPKEKLPTYSVFYEARTFGRGQPGMAEVHRGVPLGDYLFRFDFGVVAPEVCEDIWSPDGPMRRRAYSGAELVVNLSASPFRLGFVETRRELIATRAADHQCTIAYCNAVGSNDGLIFDGGGFLNQNGRHIMETPRFQEGYASAVVDLDRTLRLRAEATTWRVDRESWLASGGQAVPVLDCTQAVRTRRESLKYPVPAHRSFFLPSPDTRRTARDALCEDILDALALGVGDYFEKTRAFKVLGIALSGGRDSLLTLLIAHRYAKRARPEDPGSLIQAFYMPSRYSSDATREAAETIARELGVAFQVVSIDEAFERERDVARTMLGGKDVTPITEQNIQARLRAQRMWNWSNSCGGLFLQTGNMSEKSVGYTTIGGDLMGALAVIANVPKTVVMYLLDYLQDTTGYEGIRRVLARPAGPELAHDQVGEDELMPFPILDACFYLYGSEKLTPAEILQALTAMFPEVEAARLGGYVEKFVRLFQQSIYKWVQSPLSLHIGNLDLDRERALQLPVVTGAEWMRQG
>NZ_CP022203.1|WP_095960948.1|8144855_8146121_-|hypothetical-protein
MPRLAGCRAGNNLHVCHSTMEAWMKAKILAGAVAALMYGGVAVADDGDCPPPQASTSQSEQGTMVAQSQEDDLMGDDMLQEDDVIILETEPVPDVSGQQGGMGTGGSGTQGMDDAAMGGSGQQPSGAQGEVYMNVPVRCEPVGQQQGMGGSGQQGMGGSGQESMTPPPAAPQGTHDSEQLVVPPAPPMGTGGSGQPSTQPVYPEPESAYPPPEDATGGSGIATTPPPSSFQPSAERAEPLEVEKREDKNKMKGLSVMLGGGVEGYTGALAPQLSPGATAGVRAAIKPSKVLGLELGYTGALNNIRNAETGASGPDLVRNGGQAVLTLGIAPTAWQPYLLGGIGINDYNFRGGESLGYRDDTVGNVPAGLGLRGHVGHFVVDARANYNFLFDKDFAPGIDPAGGDFEGGGSYQGTVSIGGTF
>NZ_CP022203.1|WP_043710096.1|8144381_8144705_-|FKBP-type-peptidyl-prolyl-cis-trans-isomerase
MGLNVEDVKVGTGAEATSGKSVTVHYVGTLTSGSKFDSSRDRGQGFTFRLGAGQVIEGWDKGVAGMKVGGVRKLTIPPEMGYGARGFPPVIPPNSTLLFEVELLDVR
>NZ_CP022203.1|WP_013937513.1|8143990_8144368_-|thioredoxin
MAAVEITKDNFKETVSKEGIVILDWWASWCGPCRAFAPIFEQTSNKHPDIVFGKIDTDAQQELSGAFEIRSIPTLMVFRDGILLFEQPGALPAAALEDLLKQVRALDMEQVRKEVAARRGEPPQA
>NZ_CP022203.1|WP_095960947.1|8142561_8143797_-|hybrid-sensor-histidine-kinase/response-regulator
MPHSAFRDPPGDDTPRARILLVDDTPANLLSLEAILEPLGQELVLARSGEEALRELLRGEFACILMDVQMPGLDGLETARLIRARERTRYLPILFITALHREAAFITKGYAQGAVDYLLKPVDPDILRTKVQVFVDLYVRGEQVKRQAVELVERRRAEEAAQRASELEQQLMGIVGHDLRTPLSVVLTTAKSQLSSGALEPAQQKAFERVARSGERIQHIVDLLTDFTRSRLGDGMPVMPRAGDLNEVCREVADELQVARPGRLIRCDFSRDSLHGVWDLERMAQVVANLLDNALKYSPESSDVRLSTWEKPDVVFLEVHNEGAPIRRELLPHLFEPFRRGDASRAQARTSLGLGLYIARAVVEAHRGRLTVRSSEAGGTTFRLCLPRRADARPPVSHASEADGAPAPMSA
>NZ_CP022203.1|WP_095960946.1|8141642_8142554_+|hypothetical-protein
MLQLTTHCMNTQRRQSRKWWCAALVAWGLAGTACDNVATGDVQVTMSGGDGTQRGLPDTLFQDGWSIQFTRYLVSLGDVTLTSASGETHTSSRHVLVDVQKGDIPLVDLTGVPAGRWDVGFRVSPPEARTELADGQVSAEDLAMMRERGFSYYVEGHATKQNEPVLRFRMGFPVNALMNNCINGADGTQGIVVPEGSIARPEVTIHAEHMFYDRLGTHRGVQLRFEAIAATAGEDHVVTPEGLATQALTDLRDRDGNELRDAQGQPVIYQPGAYDVRTLQEFITQSVVDQAHLNGGGVCTVVK
>NZ_CP022203.1|WP_095960945.1|8138936_8141534_-|TonB-family-protein
MWIPTLVLCVLSATGELPVTPPVPLEAPGPVLPADVPPPEVPATVLLRLTIDRAGEVSQVEVRQSAGVAFDRAAMNAALRWRFQPARRGTEAIDVRVDVPVTFVPPVHGHHIEPVADGAEPPGAAVGHGAGDARALGGATQAGAQHQGVPGGPAPAGTEASGATGQDAQAPPSFSTTVRGAAHAPPPVAVSDFHIPVGQLADVPRRSASDLMLLAPGVMLANHGGEGHAESIYIRGFDAGEGKDVELRLNGVPLNEVSHAHGHGYADTYFIIPELVESLRVTEGPYDPSQGDFGVAGTVEYQLGLARRGLTASLATGSFAARRLSLLWGPPEASDATFVGLLLRQGHGFGPNRSYSNAGAMAQVELRVGDESRLRLFGTSYGSRFASAGVVRETDVVDTRLPCATDADSQFFCSYDPNQGGAGQRHILSAELQSRLKNGGRFVQQGYVILRQTRIRDNFTGFLQDTTPPDGETQRGDNTEGYYRGSTVGLRGRYTPGLTLLGQPQPLELGYVARYDDVRTRSRRLRDRGGVPYATVFDNQVRTTNLGAYASLRVAPLSWLTLRGGVRLDTFLFGVDDHNRPVEDRDGPRLPDESLEAYGFFASPRASAEVRLTPRLTWLTSAGLGARSSDAAALSDAELAPYARVASGETGLGWRMDGPLSLEARGAFFATRVSQDFVFDEAVGRNQPVGASQRLGAFVSARGTLRNRVDVQASLAWARATLPVPGASAWKLWDGAVMPYIPELLGRVDASLRGTTRVAGQLVDWNVALGHSAIGPRPLPLDRYSAPVFLFDVGTRARWKAVELGLSVENLLDTRWRESEFNFVSNFRGPDAPPSLMATRHFTAGAPRTFMGTLTLHLDLQEDSP
>NZ_CP022203.1|WP_013937517.1|8138100_8138940_-|hypothetical-protein
MTSPLRTTRRAFSLMLGTALVGGASACGLSGTGGRSVTFRMGLRTARAPGEDALGEFTTDTGWRVRLSSGLMVLGPIYIFENASPLEPTASAPRVLRRLGQWLLPSAHAHDGHFFSGGTVLGEWDREVVFDLLAEAGEVRELGRSPGIAGLARSFSLLLQPPSRALGAEGAVLGGRSMILEGTASREEAQVPFRVALDFPPPVELQRVDFVPIAVELDEGGRFIVEVQPHRWFEGAHFDRVTVPASGEPAELTPETQVYRALTLNVRRYTAFAGTWEPA
>NZ_CP022203.1|WP_095960944.1|8136845_8138093_+|sterol-desaturase-family-protein
MSINVYAIATPFVIVLALGEFAYCVIRRNGYYAFQDSIASMGTAVLNQCVNVAVALLVLPLFIQLGQLAPWRLGASSPLELVALFLGVDFLFYWFHRFGHRTNIGWAAHSPHHSTEELNYAVALRASVTQRLFSFLFYWPLVLVGFPPEAVLAMVAFHLVLQFIPHTRVIPKLPRWIESWLNTPSHHRVHHARNDVYIDKNYAGFLIIWDKLFGTFEEEKEACSYGLTSPPNTWDPTVINFQAWAKLVGDALATKSHWDRLRIWVMPTGWRPADLPPRPSVGWQKDGVELKFQSTELPGTRAYLVFQLLAAMPFMLLVSHHASPLSGWQKLVLSLLFWAMATAWSGMLESRRWSLPLELGRVLAMGVAVTWWLLRSPAPQSWSALCAGWLLASLVWLLVVRTAAHTATPMPQGTR
>NZ_CP022203.1|WP_095960950.1|8150304_8152836_-|MASE1-domain-containing-protein
MPRLAWPSDTRRVGGRVSGGWVIFGLLRATVRGVQGRHLLEMLGLAVVYLLAGALGQKVVSVGNISPAWPPAGVALAALGVLGVSRWPGVFVGASLMAFLSGASAAAALGVGVGNTLAAVLGLGLLRWVGFDKGLERIRDVVALCAGAGALCLGVSAVVGTASLVLGGRVPWSSLAAGLRVWWVGDLMGVLVVAPPLMLFRRWAWPRRGGEAVVLASLTTVLGGAIFFMPELPHSAAHAATFLLFPMSAWAALRFGPRGAAAATLCISAASIVGTARGHGPFATDDLTQDLLVLQLFIATNAVTGLLLAAASTERQRAIGQLQLLGTTVRSVHEGVLIAEVRGGGALRTVFANQALCSLLGYRLEELVGQDPCALYGAQGPEFRQRTRQSLLAGEPVFAEVQLTRKEGDLVWSEVLLSPVRATGEDTTHFVATHRDISATKELQARLVAAERVAAVGTLAAGVGHEINNPLAYLVLNLEAAERGLTQGGMTGMREAMSSVRGALEGAERIRLIVRDLQVFSRQENQDRGLVDLNALVPPAVRIISHALRGRARLVEEFGPVPRVSGSEARLGQVLLNLLVNAMQAIPEGNPSLNEVRVRTSTDASGRARVDVVDSGAGIPAHVLPRIFEAFYTTKSSGEGTGLGLAICQQIVRAHGGELEVRSEPGRGSVFSVLLPPARVQAPAPPRPLPRVSPPQPPPGARRGRVLVVDDEPRLAQSMRLLLEPFHDVVTTTRGGEALALVDAGHRFDVILCDLQMPETDGAAVYQHLCAHAPDQAARVVFISGGAYTPESRAFIDSVPLRVLEKPVRPDVLMGTVDAALAAGAEPSGADASPAAAVGGARH
>NZ_CP022203.1|WP_043712729.1|8152953_8153175_+|hypothetical-protein
MSRPAIAALLSFLIPGVGQIYNGDLLRGLFWLIITPGFWIGTGGCLGWVCHIVAAVTAHNRAEDKEKFRVTVV
>NZ_CP022203.1|WP_095960951.1|8153188_8153776_-|putative-glycolipid-binding-domain-containing-protein
MNAEVSHHGIRALVWRRLLSPGSEYFELRARPEGWVLAGSVVFVDGGLPHFVEYTVTTNAAWETQTVHVLRRNGDGEARLQLRVDGERRWWKGDEEVAHLRGCPDIDVACTPSTNTLPIRRLGLAVGQAADVRAAWLRIPSLALEVLPQRYTRLAETRYRYESNGGRFVAEVDVDADGVVTHYPPGWERVAVTGG
>NZ_CP022203.1|WP_095960952.1|8153800_8154460_-|HAD-family-hydrolase
MLLRAVIFDLDGTLVDSLGDIADATNHALAHHGLPTHPESAYLRFVGSGVRELIRRAVPAGQDALIEPVLATYKAYYDDHLFDRTVHYPGIPELLAALAEQGARLAVLSNKSDGFVKRLVARLLPRVPFAAVYGERPELPRKPDPAAALALASELGVPPSACAFVGDSSIDMDTARAAGMYAVGVAWGFREVHELRAHGARAVAATAAELLSALRDARP
>NZ_CP022203.1|WP_013937503.1|8154549_8155134_-|biopolymer-transporter-ExbD
MAIQVPGKRYGKRLQHSKVFGHGATAKKSGYSDLLITPLVDMFIIIVLFLIANFSATGEVLMMTKDIELPEAVNVQEVEMHPVVMVSGEQISVSGTIIGRVEDFTKDEYLNIPSLEEKLRDMKKQYEDLHSMAQDTANTFKGDINIQAHKDVEYSIIKRVMFSCATAGYNNINFAVITAGGGDAEKEASAKATP
>NZ_CP022203.1|WP_013937502.1|8155159_8155648_-|biopolymer-transporter-ExbD
MAGGMDTGGGKGGKKSLDTSINLTAFIDLMAVTISFLIMTAVWTQIGRLQVSQAGGPSTEEEQQQEEQTKTVQLNLLITPTELRLSADQSAFEPIPLTKDAKGKTDLSKLVARFKELKAQLPDQSAITLQPEDKVRYEDLVRIIDECIGAGLPQVSVSAAMG
>NZ_CP022203.1|WP_013937501.1|8155770_8156508_-|MotA/TolQ/ExbB-proton-channel-family-protein
MNLASVTNLTVLANVGGPQRGFFEEVAMRWEAGQWGMYPIAACLIVALAIMVERSIILFGKASINKEAFLRGLKKHIYAGDLDKAINYVAGQKSTPLTNVIKAGLMNVPKGNDEVQAALDEASLRETPKIEARTGYLAMLGNAAMLAGLLGTVSGLIACFEAVANVNPADKATILANGISEAMNCTGFGLLTAIPALIAFSVLTGRTQSLINDINETSVSVLNLIVANKDKFKNLNVPTSARDDE
>NZ_CP022203.1|WP_013937500.1|8156833_8157712_+|general-secretion-pathway-protein-GspE
MARKRIGELLLEQRAISVAQLEAGLAAHRKSGQRLGATLIAQGAITEATLAGALSQALGMQRVDLSATTPEWAAVHMLRARFCEQHDLFPIALESVGGRKQLVVAMSDPLNVTAVEEIEFTTGLKVSPRVAPLSTVRGAILRYYHKVPVAAPSATRPVAPARPAAKPVKAAPPAAAPPPEDDEEVIIGEELPPGEATQRTSLAELIRAREEQSRQKRGQGGAAKPKAAAANAGGVLDDLDYLFGQAREDPDRIEELERKFWALMRIMARKGLLTNEEFTRELDDEDKASGES
>NZ_CP022203.1|WP_095960953.1|8157939_8159049_+|bifunctional-methionine-sulfoxide-reductase-B/A-protein
MTTAPPSLARRFLPLALAALAALSACTQAHGAAPASPAPTIQDSRRYEKPSDAELRRTLSPLAYEVTQQGATEPAFRNPLWNHHEEGLYVDVVSGEPLFSSRDKFDSGTGWPSFTRPVDGARVVEKKDTTQGMERVEVRSKAAGSHLGHVFGDGPGPTKLRYCINSAALRFVSVNDLAKEGYGAWLPLFGRPAPAAAAKRPDASPFTETALLAGGCFWGMEDLLRKIPGVVRTEVGYTGGSSAFAKPTYRDVSSGKTGHAEAVRVVFDPTRLTYETLLEQWFFRMHDPTTLNRQGNDVGTQYRSAIFYLSDAQKRVAEAVKARVDASRKWPRPVVTQVVPATAFTPAEDYHQDYLVKNPGGYTCHYLRD
>NZ_CP022203.1|WP_095960954.1|8159058_8160978_-|PAS-domain-S-box-protein
MKTETRAVRIAGGGPAPESFQALFEALDAPAAMCDPALRLVSVNAAFRRFCADQHASVEEVARTLAGASVPADGASCDVELLPDLPGVVLTLSRRGDVVAVRARNEPELSRNRLVVAERALLEQARTEGVLLDLGRSVAEAGGEEELVAAVARGVKELFPGRSFCIRITDARTGGLTSLYAEGRLKEGAHEPLVLMERAVEKTSLDRASLPGDRVAVLSEVPLLFQDSTHGVSAPLVASGQLFGAINMEYPAGFVSDVPHDERVLLQLANQVAVAVKNAKLIDELTFVRKYLEDLLEKANALILVANRDKQVVVFNQALSALTGFGKEEVLGRDFFWLIPESEHLRLNQVIGAAIRGEPVNSFETRLLTRNGAEVRVSFATSSKLSQHGEVEGVIAIGQDITVVKELEKRIIHAEKLASIGQLAASVVHEINNPMTAVATYADALLQRSRMTPGANPADQEKLRKILESSHRILRFTRDLVSYARPAQDRPERVQLNAVVDMAVGFCEHVVSQARVSVQREYAELPPLSAVRANLVQVFVNLITNACHAMPPGGSVILATGRDGQDAVVKVRDTGTGIDPKHLQRIFEPFFTTKPEGKGTGLGLSICQGIVENHGGRMTVESTLGEGTTFIVRLPLQQG

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Crispr_ID: NZ_CP022203_15

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_15

8151308-8151499

Orphan

Consensus_repeat	Method
ACGCGCTCGGCGGCCTCCAGG	PILER-CR

2 spacers

The CRISPR arrays of NZ_CP022203_15

>merge|NZ_CP022203|15|8151308-8151499|PILER-CR
ATGCGCTCGGCGCCCTCCAGCGCGCCCCGCACGCTGGACATCGCCTCGCGCATGCCCGTCATCCCGCCCTGCGTCAGGCCACGCTCGGCGGCCTCCAGGTTCAGCACCAGGTAGGCCAGCGGGTTGTTGATTTCGTGCCCCACGCCGGCCGCGAGCGTCCCCACCGCGGCCACGCGCTCGGCGGCCACCAGG

>NZ_CP022203|15|2|8151308-8151499|PILER-CR
ATGCGCTCGGCGCCCTCCAGC	GCGCCCCGCACGCTGGACATCGCCTCGCGCATGCCCGTCATCCCGCCCTGCGTCAGG
CCACGCTCGGCGGCCTCCAGG	TTCAGCACCAGGTAGGCCAGCGGGTTGTTGATTTCGTGCCCCACGCCGGCCGCGAGCGTCCCCACCGCGGCC
ACGCGCTCGGCGGCCACCAGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095960948.1\|8144855_8146121_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|369943
NZ_CP022203.1\|WP_095960954.1\|8159058_8160978_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP022203.1\|WP_095960945.1\|8138936_8141534_-\|TonB-family-protein	unknown	unknown	gnl\|CDD\|238657
NZ_CP022203.1\|WP_043712729.1\|8152953_8153175_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013937517.1\|8138100_8138940_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_013937502.1\|8155159_8155648_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP022203.1\|WP_013937513.1\|8143990_8144368_-\|thioredoxin	unknown	unknown	gnl\|CDD\|239245
NZ_CP022203.1\|WP_013937508.1\|8149147_8150137_+\|alpha/beta-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|370661
NZ_CP022203.1\|WP_013937509.1\|8148191_8148848_-\|LON-peptidase-substrate-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|366967
NZ_CP022203.1\|WP_043710096.1\|8144381_8144705_-\|FKBP-type-peptidyl-prolyl-cis-trans-isomerase	unknown	unknown	gnl\|CDD\|223619
NZ_CP022203.1\|WP_095960946.1\|8141642_8142554_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095960952.1\|8153800_8154460_-\|HAD-family-hydrolase	unknown	unknown	gnl\|CDD\|223620
NZ_CP022203.1\|WP_095960951.1\|8153188_8153776_-\|putative-glycolipid-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|377662
NZ_CP022203.1\|WP_013937500.1\|8156833_8157712_+\|general-secretion-pathway-protein-GspE	unknown	unknown	gnl\|CDD\|274186
NZ_CP022203.1\|WP_095960949.1\|8146217_8148110_-\|NAD(+)-synthase	unknown	unknown	gnl\|CDD\|237577
NZ_CP022203.1\|WP_095960947.1\|8142561_8143797_-\|hybrid-sensor-histidine-kinase/response-regulator	unknown	unknown	gnl\|CDD\|223715
NZ_CP022203.1\|WP_170114837.1\|8160967_8162881_-\|PAS-domain-S-box-protein	unknown	unknown	gnl\|CDD\|236901
NZ_CP022203.1\|WP_095960953.1\|8157939_8159049_+\|bifunctional-methionine-sulfoxide-reductase-B/A-protein	unknown	unknown	gnl\|CDD\|235499
NZ_CP022203.1\|WP_013937503.1\|8154549_8155134_-\|biopolymer-transporter-ExbD	unknown	unknown	gnl\|CDD\|376792
NZ_CP022203.1\|WP_013937501.1\|8155770_8156508_-\|MotA/TolQ/ExbB-proton-channel-family-protein	unknown	unknown	gnl\|CDD\|376576

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095960948.1\|8144855_8146121_-\|hypothetical-protein	gnl\|CDD\|369943	pfam08549, SWI-SNF_Ssr4, Fungal domain of unknown function (DUF1750). This is a fungal domain of unknown function.	2.15645e-05
NZ_CP022203.1\|WP_095960954.1\|8159058_8160978_-\|PAS-domain-S-box-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	2.54083e-78
NZ_CP022203.1\|WP_095960945.1\|8138936_8141534_-\|TonB-family-protein	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.	5.83427e-18
NZ_CP022203.1\|WP_013937513.1\|8143990_8144368_-\|thioredoxin	gnl\|CDD\|239245	cd02947, TRX_family, TRX family; composed of two groups: Group I, which includes proteins that exclusively encode a TRX domain; and Group II, which are composed of fusion proteins of TRX and additional domains. Group I TRX is a small ancient protein that alter the redox state of target proteins via the reversible oxidation of an active site dithiol, present in a CXXC motif, partially exposed at the protein's surface. TRX reduces protein disulfide bonds, resulting in a disulfide bond at its active site. Oxidized TRX is converted to the active form by TRX reductase, using reducing equivalents derived from either NADPH or ferredoxins. By altering their redox state, TRX regulates the functions of at least 30 target proteins, some of which are enzymes and transcription factors. It also plays an important role in the defense against oxidative stress by directly reducing hydrogen peroxide and certain radicals, and by serving as a reductant for peroxiredoxins. At least two major types of functional TRXs have been reported in most organisms; in eukaryotes, they are located in the cytoplasm and the mitochondria. Higher plants contain more types (at least 20 TRX genes have been detected in the genome of Arabidopsis thaliana), two of which (types f amd m) are located in the same compartment, the chloroplast. Also included in the alignment are TRX-like domains which show sequence homology to TRX but do not contain the redox active CXXC motif. Group II proteins, in addition to either a redox active TRX or a TRX-like domain, also contain additional domains, which may or may not possess homology to known proteins.	1.03122e-36
NZ_CP022203.1\|WP_013937502.1\|8155159_8155648_-\|biopolymer-transporter-ExbD	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	1.79226e-16
NZ_CP022203.1\|WP_013937508.1\|8149147_8150137_+\|alpha/beta-hydrolase-family-protein	gnl\|CDD\|370661	pfam09752, DUF2048, Abhydrolase domain containing 18. The proteins in this family are conserved from plants to vertebrates. The function is unknown.	4.08092e-60
NZ_CP022203.1\|WP_013937509.1\|8148191_8148848_-\|LON-peptidase-substrate-binding-domain-containing-protein	gnl\|CDD\|366967	pfam02190, LON_substr_bdg, ATP-dependent protease La (LON) substrate-binding domain. This domain has been shown to be part of the PUA superfamily. This domain represents a general protein and polypeptide interaction domain for the ATP-dependent serine peptidase, LON, Peptidase_S16, pfam05362. ATP-dependent Lon proteases are conserved in all living organisms and catalyze rapid turnover of short-lived regulatory proteins and many damaged or denatured proteins.	2.0712e-27
NZ_CP022203.1\|WP_043710096.1\|8144381_8144705_-\|FKBP-type-peptidyl-prolyl-cis-trans-isomerase	gnl\|CDD\|223619	COG0545, FkpA, FKBP-type peptidyl-prolyl cis-trans isomerases 1 [Posttranslational modification, protein turnover, chaperones].	4.4775e-53
NZ_CP022203.1\|WP_095960952.1\|8153800_8154460_-\|HAD-family-hydrolase	gnl\|CDD\|223620	COG0546, Gph, Predicted phosphatases [General function prediction only].	2.5137e-52
NZ_CP022203.1\|WP_095960951.1\|8153188_8153776_-\|putative-glycolipid-binding-domain-containing-protein	gnl\|CDD\|377662	pfam06475, Glycolipid_bind, Putative glycolipid-binding. This family has a novel fold known as a spiral beta-roll, consisting of a 15-stranded beta sheet wrapped around a single alpha helix. It forms dimers. It has some structural similarity to the E. coli lipoprotein localization factors LolA and LolB. Its structure suggests that it may have a role in glycolipid binding. Its genomic context supports a role in glycolipid metabolism.	1.12646e-56
NZ_CP022203.1\|WP_013937500.1\|8156833_8157712_+\|general-secretion-pathway-protein-GspE	gnl\|CDD\|274186	TIGR02538, Type_IV_pilus_assembly_protein_PilF, type IV-A pilus assembly ATPase PilB. This model describes a protein of type IV pilus biogenesis designated PilB in Pseudomonas aeruginosa but PilF in Neisseria gonorrhoeae; the more common usage, reflected here, is PilB. This protein is an ATPase involved in protein export for pilin assembly and is closely related to GspE (TIGR02533) of type II secretion, also called the main terminal branch of the general secretion pathway. Note that type IV pilus systems are often divided into type IV-A and IV-B, with the latter group including bundle-forming pilus, mannose-sensitive hemagglutinin, etc. Members of this family are found in type IV-A systems. [Cell envelope, Surface structures, Protein fate, Protein and peptide secretion and trafficking].	1.71469e-19
NZ_CP022203.1\|WP_095960949.1\|8146217_8148110_-\|NAD(+)-synthase	gnl\|CDD\|237577	PRK13981, PRK13981, NAD synthetase; Provisional.	5.46947e-107
NZ_CP022203.1\|WP_095960947.1\|8142561_8143797_-\|hybrid-sensor-histidine-kinase/response-regulator	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	3.5955e-44
NZ_CP022203.1\|WP_170114837.1\|8160967_8162881_-\|PAS-domain-S-box-protein	gnl\|CDD\|236901	PRK11360, PRK11360, two-component system sensor histidine kinase AtoS.	1.12721e-15
NZ_CP022203.1\|WP_095960953.1\|8157939_8159049_+\|bifunctional-methionine-sulfoxide-reductase-B/A-protein	gnl\|CDD\|235499	PRK05550, PRK05550, bifunctional methionine sulfoxide reductase B/A protein; Provisional.	9.96208e-161
NZ_CP022203.1\|WP_013937503.1\|8154549_8155134_-\|biopolymer-transporter-ExbD	gnl\|CDD\|376792	pfam02472, ExbD, Biopolymer transport protein ExbD/TolR. This group of proteins are membrane bound transport proteins essential for ferric ion uptake in bacteria. The Pfam family consists of ExbD, and TolR which are involved in TonB-dependent transport of various receptor bound substrates including colicins.	1.61423e-13
NZ_CP022203.1\|WP_013937501.1\|8155770_8156508_-\|MotA/TolQ/ExbB-proton-channel-family-protein	gnl\|CDD\|376576	pfam01618, MotA_ExbB, MotA/TolQ/ExbB proton channel family. This family groups together integral membrane proteins that appear to be involved translocation of proteins across a membrane. These proteins are probably proton channels. MotA is an essential component of the flageller motor that uses a proton gradient to generate rotational motion in the flageller. ExbB is part of the TonB-dependent transduction complex. The TonB complex uses the proton gradient across the inner bacterial membrane to transport large molecules across the outer bacterial membrane.	3.94646e-23

>NZ_CP022203.1|WP_013937508.1|8149147_8150137_+|alpha/beta-hydrolase-family-protein
MPRVLRTHPVDVLFAGLSRRARLFSQGWGDEAFLEEVAAAAPFQERPLPIAPEWSAPRLQRGLRVRDGTFPSPLARLDVAARTAHVRWLSAGQGPSRGACVVLAASREEGFSLRERMYAPLAREGLDLFLLENPYYGLRRPVGQKGGALRTVSDHVLMNLGMVDEARALLAWLRGEGHARLGVAGYSMGGYMAALTAAVVPEPLAVAALAAGASPVPVFTQGLLSWSIAFALLDGPRRDAEQARLRLGRIFDLANLTRFPPPRQPEAAVLVACRRDGFVPGDETLALHAHWPRSELRWVDAGHVTALFTERAALCAAIRDSLARVDAAA
>NZ_CP022203.1|WP_013937509.1|8148191_8148848_-|LON-peptidase-substrate-binding-domain-containing-protein
MTAQERIERAASALKVFPLPSAVLFPHTVIPLHIFEPRYRALVRDALAGDRVLALSQLEPGWEGNYGGKPPMLPMMCAGVIVWDEQVEEGRYNILLQGVSRVRMTSELTTEKAYREVLAEALPDVPYEGPEEEQLRQAVFELAGRVPPSFAENLLPVAARAQGGMLADVVASAVIPEPERRQALLAELDVRKRLEGVLEDVGALIGRLQPLRPTGPLN
>NZ_CP022203.1|WP_095960949.1|8146217_8148110_-|NAD(+)-synthase
MRLVKLGLASVNTTVGAFTRNTDRALALAGKMAAEGVTLGVFQEQVIAGYPAEDMVQWQGFMDRQWPELERFARETASLSTVFVVGVGVAHQGLRLNCAAVVAGGRILGLVPKEKLPTYSVFYEARTFGRGQPGMAEVHRGVPLGDYLFRFDFGVVAPEVCEDIWSPDGPMRRRAYSGAELVVNLSASPFRLGFVETRRELIATRAADHQCTIAYCNAVGSNDGLIFDGGGFLNQNGRHIMETPRFQEGYASAVVDLDRTLRLRAEATTWRVDRESWLASGGQAVPVLDCTQAVRTRRESLKYPVPAHRSFFLPSPDTRRTARDALCEDILDALALGVGDYFEKTRAFKVLGIALSGGRDSLLTLLIAHRYAKRARPEDPGSLIQAFYMPSRYSSDATREAAETIARELGVAFQVVSIDEAFERERDVARTMLGGKDVTPITEQNIQARLRAQRMWNWSNSCGGLFLQTGNMSEKSVGYTTIGGDLMGALAVIANVPKTVVMYLLDYLQDTTGYEGIRRVLARPAGPELAHDQVGEDELMPFPILDACFYLYGSEKLTPAEILQALTAMFPEVEAARLGGYVEKFVRLFQQSIYKWVQSPLSLHIGNLDLDRERALQLPVVTGAEWMRQG
>NZ_CP022203.1|WP_095960948.1|8144855_8146121_-|hypothetical-protein
MPRLAGCRAGNNLHVCHSTMEAWMKAKILAGAVAALMYGGVAVADDGDCPPPQASTSQSEQGTMVAQSQEDDLMGDDMLQEDDVIILETEPVPDVSGQQGGMGTGGSGTQGMDDAAMGGSGQQPSGAQGEVYMNVPVRCEPVGQQQGMGGSGQQGMGGSGQESMTPPPAAPQGTHDSEQLVVPPAPPMGTGGSGQPSTQPVYPEPESAYPPPEDATGGSGIATTPPPSSFQPSAERAEPLEVEKREDKNKMKGLSVMLGGGVEGYTGALAPQLSPGATAGVRAAIKPSKVLGLELGYTGALNNIRNAETGASGPDLVRNGGQAVLTLGIAPTAWQPYLLGGIGINDYNFRGGESLGYRDDTVGNVPAGLGLRGHVGHFVVDARANYNFLFDKDFAPGIDPAGGDFEGGGSYQGTVSIGGTF
>NZ_CP022203.1|WP_043710096.1|8144381_8144705_-|FKBP-type-peptidyl-prolyl-cis-trans-isomerase
MGLNVEDVKVGTGAEATSGKSVTVHYVGTLTSGSKFDSSRDRGQGFTFRLGAGQVIEGWDKGVAGMKVGGVRKLTIPPEMGYGARGFPPVIPPNSTLLFEVELLDVR
>NZ_CP022203.1|WP_013937513.1|8143990_8144368_-|thioredoxin
MAAVEITKDNFKETVSKEGIVILDWWASWCGPCRAFAPIFEQTSNKHPDIVFGKIDTDAQQELSGAFEIRSIPTLMVFRDGILLFEQPGALPAAALEDLLKQVRALDMEQVRKEVAARRGEPPQA
>NZ_CP022203.1|WP_095960947.1|8142561_8143797_-|hybrid-sensor-histidine-kinase/response-regulator
MPHSAFRDPPGDDTPRARILLVDDTPANLLSLEAILEPLGQELVLARSGEEALRELLRGEFACILMDVQMPGLDGLETARLIRARERTRYLPILFITALHREAAFITKGYAQGAVDYLLKPVDPDILRTKVQVFVDLYVRGEQVKRQAVELVERRRAEEAAQRASELEQQLMGIVGHDLRTPLSVVLTTAKSQLSSGALEPAQQKAFERVARSGERIQHIVDLLTDFTRSRLGDGMPVMPRAGDLNEVCREVADELQVARPGRLIRCDFSRDSLHGVWDLERMAQVVANLLDNALKYSPESSDVRLSTWEKPDVVFLEVHNEGAPIRRELLPHLFEPFRRGDASRAQARTSLGLGLYIARAVVEAHRGRLTVRSSEAGGTTFRLCLPRRADARPPVSHASEADGAPAPMSA
>NZ_CP022203.1|WP_095960946.1|8141642_8142554_+|hypothetical-protein
MLQLTTHCMNTQRRQSRKWWCAALVAWGLAGTACDNVATGDVQVTMSGGDGTQRGLPDTLFQDGWSIQFTRYLVSLGDVTLTSASGETHTSSRHVLVDVQKGDIPLVDLTGVPAGRWDVGFRVSPPEARTELADGQVSAEDLAMMRERGFSYYVEGHATKQNEPVLRFRMGFPVNALMNNCINGADGTQGIVVPEGSIARPEVTIHAEHMFYDRLGTHRGVQLRFEAIAATAGEDHVVTPEGLATQALTDLRDRDGNELRDAQGQPVIYQPGAYDVRTLQEFITQSVVDQAHLNGGGVCTVVK
>NZ_CP022203.1|WP_095960945.1|8138936_8141534_-|TonB-family-protein
MWIPTLVLCVLSATGELPVTPPVPLEAPGPVLPADVPPPEVPATVLLRLTIDRAGEVSQVEVRQSAGVAFDRAAMNAALRWRFQPARRGTEAIDVRVDVPVTFVPPVHGHHIEPVADGAEPPGAAVGHGAGDARALGGATQAGAQHQGVPGGPAPAGTEASGATGQDAQAPPSFSTTVRGAAHAPPPVAVSDFHIPVGQLADVPRRSASDLMLLAPGVMLANHGGEGHAESIYIRGFDAGEGKDVELRLNGVPLNEVSHAHGHGYADTYFIIPELVESLRVTEGPYDPSQGDFGVAGTVEYQLGLARRGLTASLATGSFAARRLSLLWGPPEASDATFVGLLLRQGHGFGPNRSYSNAGAMAQVELRVGDESRLRLFGTSYGSRFASAGVVRETDVVDTRLPCATDADSQFFCSYDPNQGGAGQRHILSAELQSRLKNGGRFVQQGYVILRQTRIRDNFTGFLQDTTPPDGETQRGDNTEGYYRGSTVGLRGRYTPGLTLLGQPQPLELGYVARYDDVRTRSRRLRDRGGVPYATVFDNQVRTTNLGAYASLRVAPLSWLTLRGGVRLDTFLFGVDDHNRPVEDRDGPRLPDESLEAYGFFASPRASAEVRLTPRLTWLTSAGLGARSSDAAALSDAELAPYARVASGETGLGWRMDGPLSLEARGAFFATRVSQDFVFDEAVGRNQPVGASQRLGAFVSARGTLRNRVDVQASLAWARATLPVPGASAWKLWDGAVMPYIPELLGRVDASLRGTTRVAGQLVDWNVALGHSAIGPRPLPLDRYSAPVFLFDVGTRARWKAVELGLSVENLLDTRWRESEFNFVSNFRGPDAPPSLMATRHFTAGAPRTFMGTLTLHLDLQEDSP
>NZ_CP022203.1|WP_013937517.1|8138100_8138940_-|hypothetical-protein
MTSPLRTTRRAFSLMLGTALVGGASACGLSGTGGRSVTFRMGLRTARAPGEDALGEFTTDTGWRVRLSSGLMVLGPIYIFENASPLEPTASAPRVLRRLGQWLLPSAHAHDGHFFSGGTVLGEWDREVVFDLLAEAGEVRELGRSPGIAGLARSFSLLLQPPSRALGAEGAVLGGRSMILEGTASREEAQVPFRVALDFPPPVELQRVDFVPIAVELDEGGRFIVEVQPHRWFEGAHFDRVTVPASGEPAELTPETQVYRALTLNVRRYTAFAGTWEPA
>NZ_CP022203.1|WP_043712729.1|8152953_8153175_+|hypothetical-protein
MSRPAIAALLSFLIPGVGQIYNGDLLRGLFWLIITPGFWIGTGGCLGWVCHIVAAVTAHNRAEDKEKFRVTVV
>NZ_CP022203.1|WP_095960951.1|8153188_8153776_-|putative-glycolipid-binding-domain-containing-protein
MNAEVSHHGIRALVWRRLLSPGSEYFELRARPEGWVLAGSVVFVDGGLPHFVEYTVTTNAAWETQTVHVLRRNGDGEARLQLRVDGERRWWKGDEEVAHLRGCPDIDVACTPSTNTLPIRRLGLAVGQAADVRAAWLRIPSLALEVLPQRYTRLAETRYRYESNGGRFVAEVDVDADGVVTHYPPGWERVAVTGG
>NZ_CP022203.1|WP_095960952.1|8153800_8154460_-|HAD-family-hydrolase
MLLRAVIFDLDGTLVDSLGDIADATNHALAHHGLPTHPESAYLRFVGSGVRELIRRAVPAGQDALIEPVLATYKAYYDDHLFDRTVHYPGIPELLAALAEQGARLAVLSNKSDGFVKRLVARLLPRVPFAAVYGERPELPRKPDPAAALALASELGVPPSACAFVGDSSIDMDTARAAGMYAVGVAWGFREVHELRAHGARAVAATAAELLSALRDARP
>NZ_CP022203.1|WP_013937503.1|8154549_8155134_-|biopolymer-transporter-ExbD
MAIQVPGKRYGKRLQHSKVFGHGATAKKSGYSDLLITPLVDMFIIIVLFLIANFSATGEVLMMTKDIELPEAVNVQEVEMHPVVMVSGEQISVSGTIIGRVEDFTKDEYLNIPSLEEKLRDMKKQYEDLHSMAQDTANTFKGDINIQAHKDVEYSIIKRVMFSCATAGYNNINFAVITAGGGDAEKEASAKATP
>NZ_CP022203.1|WP_013937502.1|8155159_8155648_-|biopolymer-transporter-ExbD
MAGGMDTGGGKGGKKSLDTSINLTAFIDLMAVTISFLIMTAVWTQIGRLQVSQAGGPSTEEEQQQEEQTKTVQLNLLITPTELRLSADQSAFEPIPLTKDAKGKTDLSKLVARFKELKAQLPDQSAITLQPEDKVRYEDLVRIIDECIGAGLPQVSVSAAMG
>NZ_CP022203.1|WP_013937501.1|8155770_8156508_-|MotA/TolQ/ExbB-proton-channel-family-protein
MNLASVTNLTVLANVGGPQRGFFEEVAMRWEAGQWGMYPIAACLIVALAIMVERSIILFGKASINKEAFLRGLKKHIYAGDLDKAINYVAGQKSTPLTNVIKAGLMNVPKGNDEVQAALDEASLRETPKIEARTGYLAMLGNAAMLAGLLGTVSGLIACFEAVANVNPADKATILANGISEAMNCTGFGLLTAIPALIAFSVLTGRTQSLINDINETSVSVLNLIVANKDKFKNLNVPTSARDDE
>NZ_CP022203.1|WP_013937500.1|8156833_8157712_+|general-secretion-pathway-protein-GspE
MARKRIGELLLEQRAISVAQLEAGLAAHRKSGQRLGATLIAQGAITEATLAGALSQALGMQRVDLSATTPEWAAVHMLRARFCEQHDLFPIALESVGGRKQLVVAMSDPLNVTAVEEIEFTTGLKVSPRVAPLSTVRGAILRYYHKVPVAAPSATRPVAPARPAAKPVKAAPPAAAPPPEDDEEVIIGEELPPGEATQRTSLAELIRAREEQSRQKRGQGGAAKPKAAAANAGGVLDDLDYLFGQAREDPDRIEELERKFWALMRIMARKGLLTNEEFTRELDDEDKASGES
>NZ_CP022203.1|WP_095960953.1|8157939_8159049_+|bifunctional-methionine-sulfoxide-reductase-B/A-protein
MTTAPPSLARRFLPLALAALAALSACTQAHGAAPASPAPTIQDSRRYEKPSDAELRRTLSPLAYEVTQQGATEPAFRNPLWNHHEEGLYVDVVSGEPLFSSRDKFDSGTGWPSFTRPVDGARVVEKKDTTQGMERVEVRSKAAGSHLGHVFGDGPGPTKLRYCINSAALRFVSVNDLAKEGYGAWLPLFGRPAPAAAAKRPDASPFTETALLAGGCFWGMEDLLRKIPGVVRTEVGYTGGSSAFAKPTYRDVSSGKTGHAEAVRVVFDPTRLTYETLLEQWFFRMHDPTTLNRQGNDVGTQYRSAIFYLSDAQKRVAEAVKARVDASRKWPRPVVTQVVPATAFTPAEDYHQDYLVKNPGGYTCHYLRD
>NZ_CP022203.1|WP_095960954.1|8159058_8160978_-|PAS-domain-S-box-protein
MKTETRAVRIAGGGPAPESFQALFEALDAPAAMCDPALRLVSVNAAFRRFCADQHASVEEVARTLAGASVPADGASCDVELLPDLPGVVLTLSRRGDVVAVRARNEPELSRNRLVVAERALLEQARTEGVLLDLGRSVAEAGGEEELVAAVARGVKELFPGRSFCIRITDARTGGLTSLYAEGRLKEGAHEPLVLMERAVEKTSLDRASLPGDRVAVLSEVPLLFQDSTHGVSAPLVASGQLFGAINMEYPAGFVSDVPHDERVLLQLANQVAVAVKNAKLIDELTFVRKYLEDLLEKANALILVANRDKQVVVFNQALSALTGFGKEEVLGRDFFWLIPESEHLRLNQVIGAAIRGEPVNSFETRLLTRNGAEVRVSFATSSKLSQHGEVEGVIAIGQDITVVKELEKRIIHAEKLASIGQLAASVVHEINNPMTAVATYADALLQRSRMTPGANPADQEKLRKILESSHRILRFTRDLVSYARPAQDRPERVQLNAVVDMAVGFCEHVVSQARVSVQREYAELPPLSAVRANLVQVFVNLITNACHAMPPGGSVILATGRDGQDAVVKVRDTGTGIDPKHLQRIFEPFFTTKPEGKGTGLGLSICQGIVENHGGRMTVESTLGEGTTFIVRLPLQQG
>NZ_CP022203.1|WP_170114837.1|8160967_8162881_-|PAS-domain-S-box-protein
MAAAATRAGLRVVDGLEEASLALVDLTAPGGLAAGEALLDAALAAHLTLVVLVAPGEGAFATAQSLKPADVVTAPVALHELAWRLQCAAERHVEREEQARSQEDLALLLELTADYAETSDVEALLHGVTRRLAEKLDIARATLVMLGRSADEGIIVAASDDPTLKDLRIDLSRYPEIREVMRTGKPVVMQEASTHPLLGDVERRAVAARGIHAIAALPLPIRGQVRGVLLLRAAGRRRTFTPREIDFLTTVAHATAVALRNASVLQLVRGQTEAEKTARLAAEEQAASFKPYQLFFAHVSEGVAILDDKACVLSLNPSGAAMLDVEAPDARGRHLHQVTQPVDENVLMELVTTAARGEARSGADVQVCTRTGRRLTLSMSAAPLRDEEAATILSFRDVTDARKLEEELLQTKDFLERLIDSSVDAIIAADLKGRIILFNKGAEALCGYTAQEALGGSFTVHQLYPPGVAKRVMAMIRAPEHGGKGRLSLIREELVHRSGERVPVNMTASIVYEGGREVFSVGIFTDMRARMQLERKLSDVETRLEESEKSAVIVALAGTAAHELNQPLTSVMGYAELLKRKLKEDDFAWKPVDIIYREAERMAEIVRKIGKITRYETKSYMGAQQILDLDKATSHED

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Crispr_ID: NZ_CP022203_16

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_16

8643209-8647602

Unclear

I-A,I-B,II-B

Consensus_repeat	Method
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CRISPRCasFinder
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CRT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	PILER-CR

61 spacers

cas2,cas1,cas5,cas7,cas8b3,cas3,cas6

The CRISPR arrays of NZ_CP022203_16

>merge|NZ_CP022203|16|8643209-8647602|CRISPRCasFinder,CRT,PILER-CR
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACACCCCGAAGGCCAGGATGGCTGCCTCTGAATCATTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCAGGACACCCCACCGTGCGGCAAGGGGTACGTCGCGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCAAGCCGCGTCGTTCGCGTGGTGCTTGTTGAATAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAACGTGCGGTCGGTGCACAGCCACTGGGCGCCACCATGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTGGAAGGTGTCGCACCGCAAGGGCGTGCGCGCCTTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTGGAGGAGGTCATCACCTCCATGGCAGAGGGCGCCGAGACGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGTTGCAACCGGCGGCCTGCCGGAGGGCTCCGGGTCTACGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTGTGAGCCCACTTTCCAAACGTCTGGAAACCGTGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTGGGCTACGACTTCGGCTATCCATGGTGGCGCAAGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAAGTGTTACGTGGTGCATCTCTTCATAGATCATTCATGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCTGGCGAAGTTGTCACGGTGCATGTGAAGGACTGCAAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGGATCCTCCACAACCTCCAGCCGATCTCCGCTCATGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCCTCCGCCACCATGGCGTCGCGCTGGGGGTGGTGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGCTGCGCGACGACTTGCTGGTGGCGTCCAGTAAGCGGTGCTCAACGCCTTTCGGCATCACGGCGAGTGGGACACCGCTCAGGTCCATCGCCTCGGCATCAACCATGGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGATCCTCCGGTCCGTACTCACGAGCCCCTCAAAGATGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCACACCGGATGGTCAATGTGTTCATCATCCCACGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGTCGGCGGCGAGTCAGGGCCTGGCGCACGGCCCATGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGTTGCCCCGTATCGCCTTCGCCAGCCCCGCCGCGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGGTAACACGCTCCTCGTCAACGAGATTTTCTACAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTAGGTTCAGGGTCGACGTATGCACAAACGGTGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCTACGACTGCCATGGGCTGGGCACCCGCCGAGCAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAGCGCGGTGCCGTTCGACAGGCAGCGCCGCTGCATGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACATCCCCAGGACCACGGCTGACATACGCCTCCCACCTCGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACACCACGTTCTACACGTTCAAACCTGAGAGAAACGACGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTCCATCAAGCCCATCGCATCCAACCGCACGAAGTTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCATGGAGCCTGAACCGCCGCTGGGTCCTCTCGGCGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCTGGGGCAGGGTGACCTCTACGACCGCTACCTGGGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACACGAAACCGGGCCCTTCATGGGCATCATGAAAACGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGGTGCGTCGTCCTCGACTGCGAGGCGGACGCCGGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGTGGCTGCTGCCGCAGACGTTCAACCTCGGCATGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCATGCTCACGCGCGCGCGCTTGCTTCAGCTCCGTTTCGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGACCGCATCCTCGGGATCCTCCGGGTGGCCGAGGAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTGGGTTCACTGGTTACAGCTCGGCCGGTTCGGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACACGCGCGACACGTCAACTCGGTCGCTGTATTTAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAAGAAGGCCAAGGGCGTCAGGGCGCGGAAACTGAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTAGGCGAACCACGCCACCTCCTTGCCAGCGAAGTACGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGTGCTGCTACCGGGACGCGATGCGCACAGAAATCCAGCGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGCGTTCGGCTCCAGCATCCAGCGCGCGACGATTGGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGTCCCGCTGCGCGAGCGCGTCATCCCGCTCGTCAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGCGGCACCAGGTGCCCCGCTGTGACTCGGGCGGAGGCGAAGGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGCTTCACCACCTCCTCGTCCTCCGCCCAGGGGAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGGGTCTCACTTCGCAACAGGGAGATCTCCAATGGCTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCTCAACTCCAGCGCCGCGTCCCGCTGCGCGAGCGCGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGGGCGCGGCAGGCGGTGGAGACGCTGGTGGTCGAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCACTGGAGGTGCCCGGTGAGCGCCCCGGTGAAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTGAGAGGGGTAGAGCGTGATTTCCATGACGTCATGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACTATGCCGGTGAATAGAACGACCAAGGGCGGATACGAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCCGTCGCCGCCACCAGAGATGGACACCAGGGAGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGAGGCTGACCGCTACAGCACCCGGGAGGAAGCCGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGTTGCTCGGCTTCCGGCACGAGAAGTACGGCGACAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCTCACTGTGTCGTCTCAGACTGCACTTCCTGCTGGACGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCCTGTCCGTCGTACTCGCCCAGCGACTGGACAGCCGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGAGGGCGCTGGTTACGAGATGGTGGACTGAGAGAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGAGATGGACGTGGGTGAGCTGCGCGCCCGCTACGCGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGCATGGCGCGCGAGGCGGCATCGGGTCTGTCACGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGGGGCGCAGTCGATTCAGTTCACCTCGGGGGGGAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAGCATCTTCGTCAGGCCCTGAAGCAGAGAGGAATCCCTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACACACCACAATTCAGATCGGTACTGGCGCAGCAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCACTTCTCCGGTAGTGGGGCGCGACGAATCCGCATGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACACGATGCCGAGGATATTTGTAAGTGTTTGTTGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACC

>NZ_CP022203|16|10|8643209-8647602|CRISPRCasFinder
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACCCCGAAGGCCAGGATGGCTGCCTCTGAATCATT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CAGGACACCCCACCGTGCGGCAAGGGGTACGTCGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CAAGCCGCGTCGTTCGCGTGGTGCTTGTTGAATAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACGTGCGGTCGGTGCACAGCCACTGGGCGCCACCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGAAGGTGTCGCACCGCAAGGGCGTGCGCGCCTT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGAGGAGGTCATCACCTCCATGGCAGAGGGCGCCGAGAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTTGCAACCGGCGGCCTGCCGGAGGGCTCCGGGTCTAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGTGAGCCCACTTTCCAAACGTCTGGAAACCGTGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGGCTACGACTTCGGCTATCCATGGTGGCGCAAGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AAGTGTTACGTGGTGCATCTCTTCATAGATCATTCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTGGCGAAGTTGTCACGGTGCATGTGAAGGACTGCAA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGATCCTCCACAACCTCCAGCCGATCTCCGCTCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCTCCGCCACCATGGCGTCGCGCTGGGGGTGGTG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCTGCGCGACGACTTGCTGGTGGCGTCCAGTAAGCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGTGGGAC	ACCGCTCAGGTCCATCGCCTCGGCATCAACCATGGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GATCCTCCGGTCCGTACTCACGAGCCCCTCAAAGAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACACCGGATGGTCAATGTGTTCATCATCCCACG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTCGGCGGCGAGTCAGGGCCTGGCGCACGGCCCATG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTTGCCCCGTATCGCCTTCGCCAGCCCCGCCGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGTAACACGCTCCTCGTCAACGAGATTTTCTACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TAGGTTCAGGGTCGACGTATGCACAAACGGTGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTACGACTGCCATGGGCTGGGCACCCGCCGAGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGCGCGGTGCCGTTCGACAGGCAGCGCCGCTGCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ATCCCCAGGACCACGGCTGACATACGCCTCCCACCTC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACCACGTTCTACACGTTCAAACCTGAGAGAAACGAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TCCATCAAGCCCATCGCATCCAACCGCACGAAGTT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CATGGAGCCTGAACCGCCGCTGGGTCCTCTCGGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTGGGGCAGGGTGACCTCTACGACCGCTACCTGGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGAAACCGGGCCCTTCATGGGCATCATGAAAAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGTGCGTCGTCCTCGACTGCGAGGCGGACGCCGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTGGCTGCTGCCGCAGACGTTCAACCTCGGCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CATGCTCACGCGCGCGCGCTTGCTTCAGCTCCGTTTC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GACCGCATCCTCGGGATCCTCCGGGTGGCCGAGGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGGTTCACTGGTTACAGCTCGGCCGGTTCGGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGCGCGACACGTCAACTCGGTCGCTGTATTTA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AAGAAGGCCAAGGGCGTCAGGGCGCGGAAACTGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TAGGCGAACCACGCCACCTCCTTGCCAGCGAAGTAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTGCTGCTACCGGGACGCGATGCGCACAGAAATCCAGCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGCGTTCGGCTCCAGCATCCAGCGCGCGACGATTGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTCCCGCTGCGCGAGCGCGTCATCCCGCTCGTCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCGGCACCAGGTGCCCCGCTGTGACTCGGGCGGAGGCGAAGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCTTCACCACCTCCTCGTCCTCCGCCCAGGGGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGGTCTCACTTCGCAACAGGGAGATCTCCAATGGCT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTCAACTCCAGCGCCGCGTCCCGCTGCGCGAGCGCGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGGCGCGGCAGGCGGTGGAGACGCTGGTGGTCGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACTGGAGGTGCCCGGTGAGCGCCCCGGTGAAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGAGAGGGGTAGAGCGTGATTTCCATGACGTCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TATGCCGGTGAATAGAACGACCAAGGGCGGATACGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCGTCGCCGCCACCAGAGATGGACACCAGGGAGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGGCTGACCGCTACAGCACCCGGGAGGAAGCC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTTGCTCGGCTTCCGGCACGAGAAGTACGGCGACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTCACTGTGTCGTCTCAGACTGCACTTCCTGCTGGACG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCTGTCCGTCGTACTCGCCCAGCGACTGGACAGCCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGGGCGCTGGTTACGAGATGGTGGACTGAGAGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGATGGACGTGGGTGAGCTGCGCGCCCGCTACGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGCATGGCGCGCGAGGCGGCATCGGGTCTGTCAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGGGCGCAGTCGATTCAGTTCACCTCGGGGGGGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGCATCTTCGTCAGGCCCTGAAGCAGAGAGGAATCCCT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACACCACAATTCAGATCGGTACTGGCGCAGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACTTCTCCGGTAGTGGGGCGCGACGAATCCGCATGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGATGCCGAGGATATTTGTAAGTGTTTGTTG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACC

>NZ_CP022203|16|5|8643209-8647601|CRT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACCCCGAAGGCCAGGATGGCTGCCTCTGAATCATT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CAGGACACCCCACCGTGCGGCAAGGGGTACGTCGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CAAGCCGCGTCGTTCGCGTGGTGCTTGTTGAATAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACGTGCGGTCGGTGCACAGCCACTGGGCGCCACCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGAAGGTGTCGCACCGCAAGGGCGTGCGCGCCTT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGAGGAGGTCATCACCTCCATGGCAGAGGGCGCCGAGAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTTGCAACCGGCGGCCTGCCGGAGGGCTCCGGGTCTAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGTGAGCCCACTTTCCAAACGTCTGGAAACCGTGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGGCTACGACTTCGGCTATCCATGGTGGCGCAAGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AAGTGTTACGTGGTGCATCTCTTCATAGATCATTCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTGGCGAAGTTGTCACGGTGCATGTGAAGGACTGCAA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGATCCTCCACAACCTCCAGCCGATCTCCGCTCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCTCCGCCACCATGGCGTCGCGCTGGGGGTGGTG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCTGCGCGACGACTTGCTGGTGGCGTCCAGTAAGCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGTGGGAC	ACCGCTCAGGTCCATCGCCTCGGCATCAACCATGGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GATCCTCCGGTCCGTACTCACGAGCCCCTCAAAGAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACACCGGATGGTCAATGTGTTCATCATCCCACG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTCGGCGGCGAGTCAGGGCCTGGCGCACGGCCCATG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTTGCCCCGTATCGCCTTCGCCAGCCCCGCCGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGTAACACGCTCCTCGTCAACGAGATTTTCTACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TAGGTTCAGGGTCGACGTATGCACAAACGGTGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTACGACTGCCATGGGCTGGGCACCCGCCGAGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGCGCGGTGCCGTTCGACAGGCAGCGCCGCTGCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ATCCCCAGGACCACGGCTGACATACGCCTCCCACCTC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACCACGTTCTACACGTTCAAACCTGAGAGAAACGAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TCCATCAAGCCCATCGCATCCAACCGCACGAAGTT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CATGGAGCCTGAACCGCCGCTGGGTCCTCTCGGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTGGGGCAGGGTGACCTCTACGACCGCTACCTGGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGAAACCGGGCCCTTCATGGGCATCATGAAAAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGTGCGTCGTCCTCGACTGCGAGGCGGACGCCGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTGGCTGCTGCCGCAGACGTTCAACCTCGGCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CATGCTCACGCGCGCGCGCTTGCTTCAGCTCCGTTTC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GACCGCATCCTCGGGATCCTCCGGGTGGCCGAGGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGGTTCACTGGTTACAGCTCGGCCGGTTCGGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGCGCGACACGTCAACTCGGTCGCTGTATTTA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AAGAAGGCCAAGGGCGTCAGGGCGCGGAAACTGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TAGGCGAACCACGCCACCTCCTTGCCAGCGAAGTAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTGCTGCTACCGGGACGCGATGCGCACAGAAATCCAGCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGCGTTCGGCTCCAGCATCCAGCGCGCGACGATTGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTCCCGCTGCGCGAGCGCGTCATCCCGCTCGTCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCGGCACCAGGTGCCCCGCTGTGACTCGGGCGGAGGCGAAGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCTTCACCACCTCCTCGTCCTCCGCCCAGGGGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGGTCTCACTTCGCAACAGGGAGATCTCCAATGGCT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTCAACTCCAGCGCCGCGTCCCGCTGCGCGAGCGCGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGGCGCGGCAGGCGGTGGAGACGCTGGTGGTCGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACTGGAGGTGCCCGGTGAGCGCCCCGGTGAAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGAGAGGGGTAGAGCGTGATTTCCATGACGTCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TATGCCGGTGAATAGAACGACCAAGGGCGGATACGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCGTCGCCGCCACCAGAGATGGACACCAGGGAGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGGCTGACCGCTACAGCACCCGGGAGGAAGCC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTTGCTCGGCTTCCGGCACGAGAAGTACGGCGACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTCACTGTGTCGTCTCAGACTGCACTTCCTGCTGGACG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCTGTCCGTCGTACTCGCCCAGCGACTGGACAGCCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGGGCGCTGGTTACGAGATGGTGGACTGAGAGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGATGGACGTGGGTGAGCTGCGCGCCCGCTACGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGCATGGCGCGCGAGGCGGCATCGGGTCTGTCAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGGGCGCAGTCGATTCAGTTCACCTCGGGGGGGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGCATCTTCGTCAGGCCCTGAAGCAGAGAGGAATCCCT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACACCACAATTCAGATCGGTACTGGCGCAGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACTTCTCCGGTAGTGGGGCGCGACGAATCCGCATGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGATGCCGAGGATATTTGTAAGTGTTTGTTG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC

>NZ_CP022203|16|3|8645144-8647601|PILER-CR
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTGGGGCAGGGTGACCTCTACGACCGCTACCTGGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGAAACCGGGCCCTTCATGGGCATCATGAAAAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGTGCGTCGTCCTCGACTGCGAGGCGGACGCCGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTGGCTGCTGCCGCAGACGTTCAACCTCGGCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CATGCTCACGCGCGCGCGCTTGCTTCAGCTCCGTTTC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GACCGCATCCTCGGGATCCTCCGGGTGGCCGAGGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGGGTTCACTGGTTACAGCTCGGCCGGTTCGGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGCGCGACACGTCAACTCGGTCGCTGTATTTA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AAGAAGGCCAAGGGCGTCAGGGCGCGGAAACTGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TAGGCGAACCACGCCACCTCCTTGCCAGCGAAGTAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTGCTGCTACCGGGACGCGATGCGCACAGAAATCCAGCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGCGTTCGGCTCCAGCATCCAGCGCGCGACGATTGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTCCCGCTGCGCGAGCGCGTCATCCCGCTCGTCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCGGCACCAGGTGCCCCGCTGTGACTCGGGCGGAGGCGAAGG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GCTTCACCACCTCCTCGTCCTCCGCCCAGGGGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGGTCTCACTTCGCAACAGGGAGATCTCCAATGGCT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTCAACTCCAGCGCCGCGTCCCGCTGCGCGAGCGCGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGGCGCGGCAGGCGGTGGAGACGCTGGTGGTCGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACTGGAGGTGCCCGGTGAGCGCCCCGGTGAAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TGAGAGGGGTAGAGCGTGATTTCCATGACGTCAT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	TATGCCGGTGAATAGAACGACCAAGGGCGGATACGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCGTCGCCGCCACCAGAGATGGACACCAGGGAGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGGCTGACCGCTACAGCACCCGGGAGGAAGCC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GTTGCTCGGCTTCCGGCACGAGAAGTACGGCGACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CTCACTGTGTCGTCTCAGACTGCACTTCCTGCTGGACG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCTGTCCGTCGTACTCGCCCAGCGACTGGACAGCCG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGGGCGCTGGTTACGAGATGGTGGACTGAGAGAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GAGATGGACGTGGGTGAGCTGCGCGCCCGCTACGC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGCATGGCGCGCGAGGCGGCATCGGGTCTGTCAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGGGCGCAGTCGATTCAGTTCACCTCGGGGGGGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGCATCTTCGTCAGGCCCTGAAGCAGAGAGGAATCCCT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACACCACAATTCAGATCGGTACTGGCGCAGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CACTTCTCCGGTAGTGGGGCGCGACGAATCCGCATGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ACGATGCCGAGGATATTTGTAAGTGTTTGTTG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095961673.1\|8647756_8648905_+\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP022203.1\|WP_095961255.1\|8655056_8657294_-\|CRISPR-associated-helicase/endonuclease-Cas3	cas3	cd09639_cas3_CAS-I	gnl\|CDD\|350688
NZ_CP022203.1\|WP_095961250.1\|8649873_8650167_-\|CRISPR-associated-endonuclease-Cas2	cas2	pfam09827_cas2_CAS-I:CAS-II:CAS-III	gnl\|CDD\|187856
NZ_CP022203.1\|WP_095961249.1\|8642143_8642875_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373953
NZ_CP022203.1\|WP_095961258.1\|8658314_8659784_-\|SAVED-domain-containing-protein	unknown	unknown	gnl\|CDD\|380122
NZ_CP022203.1\|WP_095961253.1\|8652518_8653427_-\|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	cas7	cd09650_cas7_CAS-I	gnl\|CDD\|273846
NZ_CP022203.1\|WP_095961256.1\|8657290_8657902_-\|type-I-MYXAN-CRISPR-associated-protein-Cas6/Cmx6	cas6	cd09703_cas6_CAS-I:CAS-III	gnl\|CDD\|274308
NZ_CP022203.1\|WP_095961795.1\|8639307_8640519_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961248.1\|8640508_8642131_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373989
NZ_CP022203.1\|WP_157770496.1\|8632398_8633166_-\|immunity-49-family-protein	unknown	unknown	gnl\|CDD\|373949
NZ_CP022203.1\|WP_157770497.1\|8633200_8634328_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235715
NZ_CP022203.1\|WP_095961259.1\|8660109_8661033_+\|DUF2381-family-protein	unknown	unknown	gnl\|CDD\|131321
NZ_CP022203.1\|WP_095961251.1\|8650170_8651832_-\|type-I-MYXAN-CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|274899
NZ_CP022203.1\|WP_095961243.1\|8634324_8635668_-\|TIGR02270-family-protein	unknown	unknown	gnl\|CDD\|131323
NZ_CP022203.1\|WP_095961254.1\|8653455_8655072_-\|type-I-MYXAN-CRISPR-associated-Cas8a1/Cmx1	cas8b3	cd09713_cas8b3_CAS-I-B	gnl\|CDD\|187844
NZ_CP022203.1\|WP_095961245.1\|8637254_8637728_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961252.1\|8651877_8652522_-\|type-I-MYXAN-CRISPR-associated-protein-Cas5/Cmx5/DevS	cas5	cd09688_cas5_CAS-I-B	gnl\|CDD\|131635
NZ_CP022203.1\|WP_095961241.1\|8631078_8632293_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961246.1\|8637773_8638235_-\|DUF4150-domain-containing-protein	unknown	unknown	gnl\|CDD\|372665
NZ_CP022203.1\|WP_157770498.1\|8636297_8637185_-\|AHH-domain-containing-protein	unknown	unknown	gnl\|CDD\|379603

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095961673.1\|8647756_8648905_+\|IS4-family-transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain 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. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	0.000458578
NZ_CP022203.1\|WP_095961250.1\|8649873_8650167_-\|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.	2.97834e-19
NZ_CP022203.1\|WP_095961252.1\|8651877_8652522_-\|type-I-MYXAN-CRISPR-associated-protein-Cas5/Cmx5/DevS	gnl\|CDD\|131635	TIGR02586, CRISPR-associated_protein_Cas5, CRISPR-associated protein Cas5/DevS, subtype MYXAN. This model represents DevS of Myxococcus xanthus and related proteins of Leptospira interrogans and Gemmata obscuriglobus. This protein is encoded in a cluster of CRISPR-associated (cas) genes, and in the special case of Myxococcus xanthus has taken on a role in the control of fruiting body development. CRISPRs are clustered, regularly interspaced short palidromic repeats. This protein family is related to models TIGR01868, TIGR01895, and TIGR01876.	1.79288e-92
NZ_CP022203.1\|WP_095961253.1\|8652518_8653427_-\|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	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, , ].	3.18185e-60
NZ_CP022203.1\|WP_095961258.1\|8658314_8659784_-\|SAVED-domain-containing-protein	gnl\|CDD\|380122	pfam18145, SAVED, SMODS-associated and fused to various effectors sensor domain. Predicted to function as a sensor domain, sensing nucleotides or nucleotide derivatives generated by SMODS and other nucleotide synthetase domains. The sensing of ligands by SAVED is predicted to activate effectors deployed by a class of conflict systems which are reliant on the on the production and sensing of the nucleotide second messengers.	2.11261e-28
NZ_CP022203.1\|WP_095961248.1\|8640508_8642131_+\|hypothetical-protein	gnl\|CDD\|373989	pfam15648, Tox-REase-5, Restriction endonuclease fold toxin 5. A predicted toxin of the restriction endonuclease fold present in bacterial polymorphic toxin systems. In bacterial polymorphic toxin systems, the toxin is exported by the type 2, type 5, type 6, or PrsW-peptidase dependent secretion system. Versions of this domain are also found in caudoviruses.	1.13347e-18
NZ_CP022203.1\|WP_157770496.1\|8632398_8633166_-\|immunity-49-family-protein	gnl\|CDD\|373949	pfam15575, Imm49, Immunity protein 49. A predicted immunity protein with an all alpha-helical fold and a conserved proline residue. Proteins containing this domain are present in bacterial polymorphic toxin systems as an immediate gene neighbor of the toxin gene, usually containing a domain of the Tox-REAse-1 or Tox-REase-6 families.	1.42257e-09
NZ_CP022203.1\|WP_157770497.1\|8633200_8634328_-\|hypothetical-protein	gnl\|CDD\|235715	PRK06147, PRK06147, 3-oxoacyl-(acyl carrier protein) synthase; Validated.	1.39136e-35
NZ_CP022203.1\|WP_095961259.1\|8660109_8661033_+\|DUF2381-family-protein	gnl\|CDD\|131321	TIGR02268, TIGR02268, Myxococcus xanthus paralogous family TIGR02268. This family consists of at least 8 paralogs in Myxococcus xanthus, a member of the Deltaproteobacteria. The function is unknown.	8.88884e-91
NZ_CP022203.1\|WP_095961246.1\|8637773_8638235_-\|DUF4150-domain-containing-protein	gnl\|CDD\|372665	pfam13665, DUF4150, Domain of unknown function (DUF4150).	5.8713e-46
NZ_CP022203.1\|WP_095961243.1\|8634324_8635668_-\|TIGR02270-family-protein	gnl\|CDD\|131323	TIGR02270, hypothetical_protein_GSU3180, conserved hypothetical protein. Members are found in Myxococcus xanthus (six members), Geobacter sulfurreducens, and Pseudomonas aeruginosa; a short protein homologous to the N-terminal region is found in Mesorhizobium loti. All sequence are from Proteobacteria. The function is unknown. [Hypothetical proteins, Conserved].	3.85081e-50
NZ_CP022203.1\|WP_095961254.1\|8653455_8655072_-\|type-I-MYXAN-CRISPR-associated-Cas8a1/Cmx1	gnl\|CDD\|187844	cd09713, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. 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; Large proteins, some contain Zn-finger domain; signature gene for I-C subtype; also known as Csx13_N family.	5.67157e-130
NZ_CP022203.1\|WP_095961255.1\|8655056_8657294_-\|CRISPR-associated-helicase/endonuclease-Cas3	gnl\|CDD\|350688	cd17930, DEXHc_cas3, DEXH/Q-box helicase domain of Cas3. CRISPR-associated (Cas) 3 is a nuclease-helicase responsible for degradation of dsDNA. The two enzymatic units of Cas3, a histidine-aspartate (HD) nuclease and a Superfamily 2 (SF2) helicase, may be expressed from separate genes as Cas3' (SF2 helicase) and Cas3'' (HD nuclease) or may be fused as a single HD-SF2 polypeptide. The nucleolytic activity of most Cas3 enzymes is transition metal ion-dependent. Cas3 is a member of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	2.03186e-39
NZ_CP022203.1\|WP_095961249.1\|8642143_8642875_+\|hypothetical-protein	gnl\|CDD\|373953	pfam15579, Imm52, Immunity protein 52. A predicted immunity protein with an alpha+beta fold and conserved tryptophan and phenylalanine residues, and a GT motif. Proteins containing this domain are present in bacterial polymorphic toxin systems as an immediate gene neighbor of the toxin gene, usually containing a domain of the Tox-REase-5 family.	1.56654e-30
NZ_CP022203.1\|WP_095961256.1\|8657290_8657902_-\|type-I-MYXAN-CRISPR-associated-protein-Cas6/Cmx6	gnl\|CDD\|274308	TIGR02807, hypothetical_protein_LA_3189, CRISPR-associated protein Cas6, subtype MYXAN. Members of this protein family resemble the Cas6 proteins described by TIGR01877 in having a C-terminal motif GXGXXXXXGXG, where the single X of each GXG is hydrophobic and the spacer XXXXX has at least one Lys or Arg. Examples are found in cas gene operons of CRISPR regions in Anabaena variabilis ATCC 29413, Leptospira interrogans, Gemmata obscuriglobus UQM 2246, and twice in Myxococcus xanthus DK 1622. Oddly, an orphan member is found in Thiobacillus denitrificans ATCC 25259, whose genome does not seem to contain other evidence of CRISPR repeats or cas genes.	3.22589e-87
NZ_CP022203.1\|WP_095961251.1\|8650170_8651832_-\|type-I-MYXAN-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274899	TIGR03983, hypothetical_protein_LA3181, CRISPR-associated endonuclease Cas1, subtype MYXAN. Members of this protein are the Cas1 endonuclease, or Cas1 domain in Cas4/Cas1 fusion proteins, of the MYXAN subtype of CRISPR/Cas systems. These systems typically feature repeats and spacers each about 36 base pairs in length. Species with this type of CRISPR system include Myxococcus xanthus, Cyanothece sp., Leptospira interrogans, Sorangium cellulosum, Anabaena variabilis ATCC 29413, etc.	0
NZ_CP022203.1\|WP_157770498.1\|8636297_8637185_-\|AHH-domain-containing-protein	gnl\|CDD\|379603	pfam14412, AHH, A nuclease family of the HNH/ENDO VII superfamily with conserved AHH. AHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif, AHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. Like WHH and LHH, the AHH nuclease contains 4 conserved histidines of which, the first one is predicted to bind a metal-ion and the other three ones are involved in activation of a water molecule for hydrolysis.	4.66714e-05

>NZ_CP022203.1|WP_095961249.1|8642143_8642875_+|hypothetical-protein
MTERPVPEGYYAGAYWGPRKESPEECAQRAANFLNLLAPHDPLLAHWYKPARSAKDARKHPLMPPDVPTLTGLFRRGVNRERGGPAIEQLGYTLWFDNGGGKFDRAGLQILCGCYSEAVSNACVLTLPSTGPEAERVGAVPVLAGAVRSMAMTWDPDWAVATSDSFRRLMREPSKSSAFVGWVTYLSRRRGMVPPLPAPVRIEPVEDKGTLIILTPERLTARNPEHVEQGRRVCELLARAGRM
>NZ_CP022203.1|WP_095961248.1|8640508_8642131_+|hypothetical-protein
MRANALLLFVAVLATGCASLTPAPGRGRSLSYTTRGATAPPLAPSPSEEYPHAPASLPPSVAGPEVPERLSRRRGFREVATGASPGSVAGAVGGFVARGTAQEDAWEKLLTDAGLEERDERPMGGALSPTQAARLLGVLLRRPVTLGTFPPRMAVGYLLREVLEEGEVSRDELLRRVERFARVAVLRPDGYLAWTRTGRTQQKAAPVEWRDGAFRAGPFELGRFYVSNGFVFQLADERLAPVEGSVFVEVYDDADYVGRTLDGAEAAFVKLALSIGHFFTYPLDSIASLKNLPAGVAALIESSPEYFERFRYMTRGEQVQAIAELATNLLVTTGTATGTTRTITGALAGAEATVPVLSLSARGALAIERVAVPVGRAAAVLGGGPGATLILHRANTAAPGAGPSKGPGQWGPAKESMKPPARRYQEQITGHGADEAYWVGGMSAAEGGVKFDGFKDGVLLEAKGPNYANKFEDSLEPRFWFANSGAAEMVKQAQRQIESVRGMGIPIEWHVAEAKVAEAIELLFERNQVSEIRVVHTPPL
>NZ_CP022203.1|WP_095961795.1|8639307_8640519_+|hypothetical-protein
MTRLEAATLALLPRAGAGEREGFVQVEPTVILDGGPEFGLNVGAPVRLRLWGGAAGASVVRREDWDSLSDWGQLVRGLKFGSDTAPLGVWFGALEGYSLLTGHLVRRYSNRMNPDYHPAGGVLTGTVGPLYTEAFVSDVLGARLMGAELSLDMQHVLFGKPKEKGRYTLALSAVHDWGKVGGRAPSVTLAHLDATAVVLVRPGFEALVVAGWGGRPIEGGAWGAVAGVGADAVTPTLDMTLRLEVRRQHGGFRQGFFGPDYELARFHAAGPEGVPLAEAAFPEGFSLYGEAAVGWDAVSYGGRYRHLQLSLGAEAFTWGRFDVDGRVAVQLFERSLEVALKGLGVGMGQPGARYLGAAEVRWRVLRGRLYALGTGGTLLFPQGDGTLRPGAFASVGLGVEHAR
>NZ_CP022203.1|WP_095961246.1|8637773_8638235_-|DUF4150-domain-containing-protein
MANTVGVNKMSVVTKDSKGVTVAFPDVCKTPGPAGPVPIPYPNVARSADTEQGSKKVSVEGNPVCVRDSNFSTSTGDEAGSVGGVVSGTTRGKAEFVNFSFDVQFEGKSVARAFDLMLHNDRNTPPTPLMQPPVAGLGVPPEKRPCDTCGKER
>NZ_CP022203.1|WP_095961245.1|8637254_8637728_-|hypothetical-protein
MVSEEPILAPRVGWVAGASADGALWVDFKGNRRGPLLARTTVVLASEVIRRASVARQGALLLFENGDPSLPVLVGLLQRSLSAPLTEALLDSLGAGPREARVDGKQVRLEAREEVTLKCGKASLTLRRNGDVILRGVNIQTEAEQVQRIKGGKVQVN
>NZ_CP022203.1|WP_157770498.1|8636297_8637185_-|AHH-domain-containing-protein
MVNMPRTSTRKRTVKKAPLRTKVRKRHSVGGAADKKGTAVKKPKPPPSPHSWEGSYISDDHAHGCVNRHISAYTPSNPCSHRHQARLKAQQNPAKYTWPADADRQPDTVGAWDLTADGNFETHARTPFYHEAHHIVANAELQAVVAEAGEGIEPRGRVPLIVRSGLMREGYNLNSQLNMIILPMVKYAAVALGLPLHRRTPLHFHHAIYSEYIKRELRKRFSWVKKAAAEHEVPEYQATREAVELLSMEVQPQIIAAGEAMKAGTMAGDALEDIPHEFLSGGRNKGVDMLTGPPP
>NZ_CP022203.1|WP_095961243.1|8634324_8635668_-|TIGR02270-family-protein
MNTALRPSAARTAPRRPPLLWDVLTEHLEEASFLWAQRARAMGASDFTLSEVEAGDEARLRAHLDGLRVGGPPVALRLLRPALEDDEPGRVVSAASVLLAAGEQALVLARWEEDGARRPWLGHALALGEPPALDAALLELLPRLAPALQAELLDVLAFRQVDAGPLLERLALADTEPALLAAAFRAARVTQPPVLAAWLRKGLEDPRPRVRDAAIEAGLLRGLRAAWQSCQALATEGPEPRLAMLALAVGGGHADVERLVRTLDRPERRAEALWALGFSGRMAAAEAALEVLKARAPEVAWLALRTFSVITGLPPEDLFIRAEDEDEDEVASPSEAVSSLLPPPEHRSGQVRVAEVARWWAQARERFDPEGRYRAGAPWTPEALLQALHLAPMRHRPALAFELAVRSRGACQVEPRGWCGHQRARLRAARARSLERLTRGFDGWMIS
>NZ_CP022203.1|WP_157770497.1|8633200_8634328_-|hypothetical-protein
MSAPREAPPRDVLGVITAIGAVTSVGRGAAASCAAIRAGISRPRRVSHFQVLEPETQDTVPLTAHPIQGYTDGFVGMGRWLRLARGCLGEVLETPGLPRPSDARFWDRAGLLMVIPSRDDGLFELEGDDGLEGIREDCLRPLLDALGLALPDAKVWVVDQGPAGTATAVQQASGELWRAGFERVLVLAVDSLVDPEALRMLDEEGRLKVGDNPVGLMPGEAGACFLLEQEEAVRRRGAAPLALVTGVATAEERLHLYAGHVSQGAGLAACLREVLARGPVPARFEGDLYSDLNGEEWRAREWGTALVRLGDALGAHGVQLPCVSVGDVGAASGALGVCLSVHAFTRGHSRTAQSLVVSSSPWGAVGCLRLHSTGA
>NZ_CP022203.1|WP_157770496.1|8632398_8633166_-|immunity-49-family-protein
MASRFLPAVIENALHQNRALRRVLVRRAGSARHILTFCDNLRLAGIGALFLTGTSEPFLQRLQQSGRAFAHHLREVGSADLRLSRSRPLFDAVGAGDFHGAALIAQRARRTWTQGEEYEEDFLFVEFVIQHGVLDAPVAACEDLLMRYERALRGAEDLRFDVCRALLQADSEGFNQALGVFLSERKDRLEAQARTAPFPEEFLATEWSFSLEGLALVRLAERNGLETEEDYLHIPSLAREPHRTPLGEDAWMDAD
>NZ_CP022203.1|WP_095961241.1|8631078_8632293_+|hypothetical-protein
MVKDVSHKWEFKARFRRHAFGWKSQPAITRIKQAVTEIKQAAKKAPVLAAEGAVLFLERVSPALAHVDSSSGAIGTAVNHAISELVPLIASAPVDAATRDAWLERLWEAYQADDIPYIESLGHHWGTLCAAPEVASAWADRLIGTVRLAWSPSSDLRGFFKGTTNCLSALVAAGRHDDVLALLELAPYRMWHDRQYGVKALAAQGRTEEALRYAEAERNDSPYAVARACEALLLAEGRAEEAYQRHGLLANQGGTYLATFRAVARKYPHKAAGEVLADLVRSTPGEEGKWFAAAKDAGLYEEALGLARQTPCDPKTLTRAAQAFAKTQPAFALEAGLLALHWLVQGHGYEVTSLDVCDAYRATCEAAEQQGASAGARARIRALLAAGGPGRDFVAGALASELAS
>NZ_CP022203.1|WP_095961673.1|8647756_8648905_+|IS4-family-transposase
MSKSITHAEVHRFIEEAVGPDTHAKRVLSLSNATLGAVHAASLSVRAIGLALSQARGLEGKHAIKQVDRLLSNSGVDVWRLFAQWVPFVVAERKAVTVTIDWTDFESDDHTTVAIQLVTRHGRATPLLWKTVPKSELAGQRNAHEDALLERLHQVLPSDVEVTVLADRGFGDVALYELLDRLSFGYVIRFRGVVHVESAGGEVHKAKEWVPPTGRPKLLRGARVTQARFGVGAVVCVHQKGMKEAWFLAASSKEATATELVKAYGRRFTCEETHRDIKDLRFGMGLSAIAIGTCERRDRLLLLSAFAMALLTLLGAAGEATGLDRKFRADTRKTREYSLFRQGIIYYGALANMREEWLRPLMEKFAELIREQAVFREAFGFI
>NZ_CP022203.1|WP_095961250.1|8649873_8650167_-|CRISPR-associated-endonuclease-Cas2
MAEPRRWYLITYDIRDPKRWRKVHGLLKGYGEWLQLSVFRCSLTDRDREKLRWELSRRMDAVDTLLVIGLCGGCVERVRAINAKEDWPEEPAPFKVL
>NZ_CP022203.1|WP_095961251.1|8650170_8651832_-|type-I-MYXAN-CRISPR-associated-endonuclease-Cas1
MNVPVTSPKPDVAEPSIRTHALHALAYCERLFYLEEVEELRVADASVFAGRRLHVQLQEEGERVELELASEALGLHGRVDALRTREGTLVVHEHKRGRHAPGRDAPEAWPSDRLQAGAYALLVEERFPGTPVECRVRYHQTDTTVSFPLDAALRRDVAAAVSRARLLRASRERPPVTPEERKCAKCSLAPVCLPEEERSGAGEERPRLFPEDDVRLVLHVTTPGARVGKSSEQLVVTPPDGEGEPTRQPGRMVSALIAHGAVQVSAQALAYCVENDIGVHWFTSGGRYLGGLTGGAGSVHRRLRQFEALRQEAVCLGLARRLVAAKLEGQLRFLMRASRGDTESRKVLASAVRDLRELLPKCAEAPSLEVLLGLEGAGAARYFGALPYLQGEDVDARLRFDGRNRRPPRDRFNAALGFLYGLVHREVEAAIRAVGLDVAFGFYHQPRGSAGPLGLDVMELFRVPLADMPLVASVNRRAWDADADFEVTSEHVWLSKTGRAKAIELYERRKRETWKHNVLGYSLSYARLVELEVRLLEKEWTGKPGLFATFRLR
>NZ_CP022203.1|WP_095961252.1|8651877_8652522_-|type-I-MYXAN-CRISPR-associated-protein-Cas5/Cmx5/DevS
MIALELSVPVACWRKGRARELVETEVLPPPATCYGALLSLVGEQDRERHRGCRVTAGVLNAPVISTVLRTFWRSKNLKVAKGNDENAAPDQQQLVIEARLVVWCDSGEEVDSRESLEVRVIRAMLEPGTVTRSGAWSLGESTHLINDAHLLPAGRPPASCRTFLVAPAGALTLPVWVDHVGTRGSRYAVGLLEDVLEAPAVQRLPRIPLAEGAG
>NZ_CP022203.1|WP_095961253.1|8652518_8653427_-|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR
MSLHVFAAFVTPLGTAANNRGLTEGNITSLQKLVWNGQVHTTVSAESIRFALRRRLNALEPCNRTYDDALRANEWKDKDFSAWAAKSKEKTYIDDDLLGFMAAEGAKQEGDKGTAKVRRAVLEVSRAVSLTPWSGDVTFNAASPGATPSAQKKGSNPVPYGTEMHATRYQYGVALTPDALRVPARAVTALNQLCALGPVAGNHGRFLFDFSPESVVFRLTQEAAPRILYAFEPSSRPGGVELAALLRKVKSGDVPAKELVLGGQAVEGLSAEEREVLSGAELHAGVVAACRAACKRMEAGKR
>NZ_CP022203.1|WP_095961254.1|8653455_8655072_-|type-I-MYXAN-CRISPR-associated-Cas8a1/Cmx1
MAKAVSSRKKALPAPLTVRLYAPGMTPLLRAGAGGLAASLRAILGDAAPWPAPVPLGPGTATVAPEAIHLDWGGEPPEATLRALFGASFQVRQGFIDLPGTRAPGAPEPPPALAAALHDALKVTFLQHGKSTQGGARRRVTFEVDAQPVVVESQGYESFVHQTAWRDVLKALESGTTSLASWAYPGAAERHLGVRVTKVEYTAAEALCACFALVGCVSYKLPQLRGGAFVALAPTDLVRFAELRPRLTPMRLHDVAVAGAADAVLAAQLVLAQESGKRRLGAVLGTTEAVALRQMPWNAQQKIRGAVVRQDAVREAVLDRYEAAAAALPHTLRVRKPEGKAKGDAGYFIATSALRAFITENLAAARPWYAGFATATTAEGRFIHTYRDRDNLGALLWHERKGLTTMHSYLGDAEQWLVQSVHLALRARFRSIYKDTEHSPKATRSNRLKGERERLRLGFAGAKTPEQVRAALADLWSRAGSNSELQEHWREVLPLLGPERWREARDLALVALASYQSQGPEAAELESADDESAADEQS
>NZ_CP022203.1|WP_095961255.1|8655056_8657294_-|CRISPR-associated-helicase/endonuclease-Cas3
MKRLLAKSTATPDRPEGEATLLGHTALVLSAARRLLEHRGRASLLAAGLDPALEPRLRRIVLLAAALHDLGKCSEHFQSMLRRKRDAPQWVRHEALSLWLCWPGQPLSAWLLRDVSELDLGLALVCVAAHHRKFQADAFAPEDAGAGLTVELLVQHEDFTRTLARIAEELSLSAPPVFTAPLLLRATRTAHPRDQLQAWQEDFERTIPASAMDARLLAVCKALVLAADVAGSALPRSGERQDWVDRQLTAPHPGEALLAVVERRLAGRMPRPFQEAVARCAAPLTLVRAGCGSGKTAAAYLWAARQHPGRPLWLTYPTMGTATEGFRDYLHGADVDARLQHSRAEVDFDIFGLRDGAARELGSREQDRLDALRSWGVDAMSCTADTVLGLVQSQRQGLYAWPALCAACVVFDEVHAYDDRLFGCLLRFLEALPGIPALLMTASLPAARLGALREVCERVHGQRLAEVDGPEDLEALPRYQRLDVAEPWALVARCLEGNGKVLWVSNTVERCMRTAEVATSHGAHALLYHSRFRYADRVHRHGDVIETFATPDRAVFASTTQVAEMSLDLSADLLVTDLAPIAALIQRLGRLNRRSTPERPGPVRPFVVLPFDGPPYGAPDLREARAWLERLGTDPLSQQDLVDAWSPSTVASPRRASSTWLDGRFDTWPAPCRDGSPSLTVLLEKDAEDVRTGAVSAHKVTLPMNLPPDSFRWRAWPRAGRLPYPIPPAHLLEYDELRGARWRKP
>NZ_CP022203.1|WP_095961256.1|8657290_8657902_-|type-I-MYXAN-CRISPR-associated-protein-Cas6/Cmx6
MALIDLLFPVQGGPVPLDHAYLLFAALSRHIPALHERSDLGVFSLRGVSNTRELLYLGRGTLRLRCPVEAVATLLPLVSAPLEVAGRRLSLGAPSLYALEPVPSLAARLVTFKHAMDEPAFIAAASRALEALGVQATLTVGRRRIVRIADKKVVGFALDLHGLSAEHSLRVQERGLGGRRHMGCGLFLPPGRAALAQARGRAA
>NZ_CP022203.1|WP_095961258.1|8658314_8659784_-|SAVED-domain-containing-protein
MGEQSASRLEGDRYQHLLSWYELLRLLDAGSPFAHGYVEHPEAGSADDVTLHARPGAGAGSRYMQVKWHVDHRETYSVAGLVAPPRVGRSLLGKLLESWLSLRPQGPVEIWLLSNWASAEDLGRYLHGRDHCFTEAFFAQPARGALKRHWAEWQQRLGVPAETLRAFCKDLRLRLGVGGIADVEEQVDDRMGRLGLRMGRQPRAIAVDGLREWIEVGGGRKHVTAESLREALREWGLVASREDAPEVSLWIHGWARRVWERPPTEELDWTPHFDRDTRKVPSEAAWRDVLLPSLLAAKQRLSRRPDGALIDLRGKLPLSTVLAVGFHLPEVGGYRFRVEQPTRGETFLWRSDTKPSERRLRVTGHEGKADATGLLVVFQLTGDARADMERFMAERPGHFRAVLYLEPEDGPHDGAVGSDADAVAFAVQAREQLRRARNELRTGVTHLILYAPAACCLFLGQRLNAVGPVVAYERTGAGGYAPALTLETG
>NZ_CP022203.1|WP_095961259.1|8660109_8661033_+|DUF2381-family-protein
MFPPGSLVMAAVVLLLGTAAVAQTPNTKRWRRIERALVLSAGAGEPVQRLRLAPGVVTTVLLDSGAVLEGELPEALRGLFSRLDVTGTHLLLQPTVVMPAQGVPPLVLRFTDAAAPQRLVLELTTEANVVDSVVDVRRHPATVAQLEAELVALRERNALLEARLATARRQAPHPGLAGAILSGAIGITGVLETWLDAPASEAELKVRQLNSYRSGSWVAVAVKLENPPGDVPWQPGIARLTSLDSNGQPTDEPMELPLLLKEPRLLPGQSAVAVVQWPVPSRPPAAYALELWDTGRRRGARWARLKP

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Crispr_ID: NZ_CP022203_17

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_17

8648950-8649624

Unclear

I-A,I-B,II-B

Consensus_repeat	Method
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	PILER-CR
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CRISPRCasFinder
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CRT

9 spacers

cas2,cas1,cas5,cas7,cas8b3,cas3,cas6

The CRISPR arrays of NZ_CP022203_17

>merge|NZ_CP022203|17|8648950-8649624|PILER-CR,CRISPRCasFinder,CRT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAGGCGCTACGCATCATCGGCGCTTCCGGGCAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAACTTCCCGATGGCGGTGAATCGCCGGACACGGATGTGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCCATCCGCCTTTTCGAGTCCTGGATCGACCCTGCCGAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACATCGCGGCTGGGTGACGATTTCAGGCGTCCTCACGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGGCTATCGCATACTATTGTGCCTTTAGATTCAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACAACCCCACGAGGGCCGCGAGGTCCGACCCGCCCAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACGGCAACACCGTGCCCGCGTCGCCCGTCGCCGTCAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGGCGTCACCAACAACGTCAACAACGGGGTGACGAAGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGACCGTGGTGCGTGGCGGCAGGCGTCGCCGCAGGAACAGGTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC

>NZ_CP022203|17|4|8648950-8649624|PILER-CR
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGGCGCTACGCATCATCGGCGCTTCCGGGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACTTCCCGATGGCGGTGAATCGCCGGACACGGATGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCATCCGCCTTTTCGAGTCCTGGATCGACCCTGCCGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ATCGCGGCTGGGTGACGATTTCAGGCGTCCTCAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGCTATCGCATACTATTGTGCCTTTAGATTCA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACCCCACGAGGGCCGCGAGGTCCGACCCGCCCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGCAACACCGTGCCCGCGTCGCCCGTCGCCGTCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGCGTCACCAACAACGTCAACAACGGGGTGACGAA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTGGTGCGTGGCGGCAGGCGTCGCCGCAGGAACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC

>NZ_CP022203|17|11|8648950-8649624|CRISPRCasFinder
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGGCGCTACGCATCATCGGCGCTTCCGGGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACTTCCCGATGGCGGTGAATCGCCGGACACGGATGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCATCCGCCTTTTCGAGTCCTGGATCGACCCTGCCGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ATCGCGGCTGGGTGACGATTTCAGGCGTCCTCAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGCTATCGCATACTATTGTGCCTTTAGATTCA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACCCCACGAGGGCCGCGAGGTCCGACCCGCCCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGCAACACCGTGCCCGCGTCGCCCGTCGCCGTCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGCGTCACCAACAACGTCAACAACGGGGTGACGAA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTGGTGCGTGGCGGCAGGCGTCGCCGCAGGAACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC

>NZ_CP022203|17|6|8648950-8649624|CRT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AGGCGCTACGCATCATCGGCGCTTCCGGGCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACTTCCCGATGGCGGTGAATCGCCGGACACGGATGT
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CCATCCGCCTTTTCGAGTCCTGGATCGACCCTGCCGA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	ATCGCGGCTGGGTGACGATTTCAGGCGTCCTCAC
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGCTATCGCATACTATTGTGCCTTTAGATTCA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	AACCCCACGAGGGCCGCGAGGTCCGACCCGCCCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	GGCAACACCGTGCCCGCGTCGCCCGTCGCCGTCAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGGCGTCACCAACAACGTCAACAACGGGGTGACGAA
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC	CGTGGTGCGTGGCGGCAGGCGTCGCCGCAGGAACAG
GTGCTCAACGCCTTTCGGCATCACGGCGAGCGGGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095961673.1\|8647756_8648905_+\|IS4-family-transposase	unknown	unknown	gnl\|CDD\|376573
NZ_CP022203.1\|WP_095961255.1\|8655056_8657294_-\|CRISPR-associated-helicase/endonuclease-Cas3	cas3	cd09639_cas3_CAS-I	gnl\|CDD\|350688
NZ_CP022203.1\|WP_095961250.1\|8649873_8650167_-\|CRISPR-associated-endonuclease-Cas2	cas2	pfam09827_cas2_CAS-I:CAS-II:CAS-III	gnl\|CDD\|187856
NZ_CP022203.1\|WP_095961249.1\|8642143_8642875_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373953
NZ_CP022203.1\|WP_095961253.1\|8652518_8653427_-\|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	cas7	cd09650_cas7_CAS-I	gnl\|CDD\|273846
NZ_CP022203.1\|WP_095961258.1\|8658314_8659784_-\|SAVED-domain-containing-protein	unknown	unknown	gnl\|CDD\|380122
NZ_CP022203.1\|WP_095961795.1\|8639307_8640519_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961248.1\|8640508_8642131_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373989
NZ_CP022203.1\|WP_157770496.1\|8632398_8633166_-\|immunity-49-family-protein	unknown	unknown	gnl\|CDD\|373949
NZ_CP022203.1\|WP_157770497.1\|8633200_8634328_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235715
NZ_CP022203.1\|WP_095961259.1\|8660109_8661033_+\|DUF2381-family-protein	unknown	unknown	gnl\|CDD\|131321
NZ_CP022203.1\|WP_095961251.1\|8650170_8651832_-\|type-I-MYXAN-CRISPR-associated-endonuclease-Cas1	cas1	cd09634_cas1_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|274899
NZ_CP022203.1\|WP_095961243.1\|8634324_8635668_-\|TIGR02270-family-protein	unknown	unknown	gnl\|CDD\|131323
NZ_CP022203.1\|WP_095961254.1\|8653455_8655072_-\|type-I-MYXAN-CRISPR-associated-Cas8a1/Cmx1	cas8b3	cd09713_cas8b3_CAS-I-B	gnl\|CDD\|187844
NZ_CP022203.1\|WP_095961245.1\|8637254_8637728_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961252.1\|8651877_8652522_-\|type-I-MYXAN-CRISPR-associated-protein-Cas5/Cmx5/DevS	cas5	cd09688_cas5_CAS-I-B	gnl\|CDD\|131635
NZ_CP022203.1\|WP_095961260.1\|8661063_8662920_+\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP022203.1\|WP_095961256.1\|8657290_8657902_-\|type-I-MYXAN-CRISPR-associated-protein-Cas6/Cmx6	cas6	cd09703_cas6_CAS-I:CAS-III	gnl\|CDD\|274308
NZ_CP022203.1\|WP_095961246.1\|8637773_8638235_-\|DUF4150-domain-containing-protein	unknown	unknown	gnl\|CDD\|372665
NZ_CP022203.1\|WP_157770498.1\|8636297_8637185_-\|AHH-domain-containing-protein	unknown	unknown	gnl\|CDD\|379603

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095961673.1\|8647756_8648905_+\|IS4-family-transposase	gnl\|CDD\|376573	pfam01609, DDE_Tnp_1, Transposase DDE domain. Transposase proteins are necessary for efficient DNA transposition. This domain is a member of the DDE superfamily, which contain 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. This family contains transposases for IS4, IS421, IS5377, IS427, IS402, IS1355, IS5, which was original isolated in bacteriophage lambda.	0.000458578
NZ_CP022203.1\|WP_095961250.1\|8649873_8650167_-\|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.	2.97834e-19
NZ_CP022203.1\|WP_095961249.1\|8642143_8642875_+\|hypothetical-protein	gnl\|CDD\|373953	pfam15579, Imm52, Immunity protein 52. A predicted immunity protein with an alpha+beta fold and conserved tryptophan and phenylalanine residues, and a GT motif. Proteins containing this domain are present in bacterial polymorphic toxin systems as an immediate gene neighbor of the toxin gene, usually containing a domain of the Tox-REase-5 family.	1.56654e-30
NZ_CP022203.1\|WP_095961253.1\|8652518_8653427_-\|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	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, , ].	3.18185e-60
NZ_CP022203.1\|WP_095961258.1\|8658314_8659784_-\|SAVED-domain-containing-protein	gnl\|CDD\|380122	pfam18145, SAVED, SMODS-associated and fused to various effectors sensor domain. Predicted to function as a sensor domain, sensing nucleotides or nucleotide derivatives generated by SMODS and other nucleotide synthetase domains. The sensing of ligands by SAVED is predicted to activate effectors deployed by a class of conflict systems which are reliant on the on the production and sensing of the nucleotide second messengers.	2.11261e-28
NZ_CP022203.1\|WP_095961260.1\|8661063_8662920_+\|serine/threonine-protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	1.50947e-54
NZ_CP022203.1\|WP_095961248.1\|8640508_8642131_+\|hypothetical-protein	gnl\|CDD\|373989	pfam15648, Tox-REase-5, Restriction endonuclease fold toxin 5. A predicted toxin of the restriction endonuclease fold present in bacterial polymorphic toxin systems. In bacterial polymorphic toxin systems, the toxin is exported by the type 2, type 5, type 6, or PrsW-peptidase dependent secretion system. Versions of this domain are also found in caudoviruses.	1.13347e-18
NZ_CP022203.1\|WP_157770496.1\|8632398_8633166_-\|immunity-49-family-protein	gnl\|CDD\|373949	pfam15575, Imm49, Immunity protein 49. A predicted immunity protein with an all alpha-helical fold and a conserved proline residue. Proteins containing this domain are present in bacterial polymorphic toxin systems as an immediate gene neighbor of the toxin gene, usually containing a domain of the Tox-REAse-1 or Tox-REase-6 families.	1.42257e-09
NZ_CP022203.1\|WP_157770497.1\|8633200_8634328_-\|hypothetical-protein	gnl\|CDD\|235715	PRK06147, PRK06147, 3-oxoacyl-(acyl carrier protein) synthase; Validated.	1.39136e-35
NZ_CP022203.1\|WP_095961259.1\|8660109_8661033_+\|DUF2381-family-protein	gnl\|CDD\|131321	TIGR02268, TIGR02268, Myxococcus xanthus paralogous family TIGR02268. This family consists of at least 8 paralogs in Myxococcus xanthus, a member of the Deltaproteobacteria. The function is unknown.	8.88884e-91
NZ_CP022203.1\|WP_095961246.1\|8637773_8638235_-\|DUF4150-domain-containing-protein	gnl\|CDD\|372665	pfam13665, DUF4150, Domain of unknown function (DUF4150).	5.8713e-46
NZ_CP022203.1\|WP_095961243.1\|8634324_8635668_-\|TIGR02270-family-protein	gnl\|CDD\|131323	TIGR02270, hypothetical_protein_GSU3180, conserved hypothetical protein. Members are found in Myxococcus xanthus (six members), Geobacter sulfurreducens, and Pseudomonas aeruginosa; a short protein homologous to the N-terminal region is found in Mesorhizobium loti. All sequence are from Proteobacteria. The function is unknown. [Hypothetical proteins, Conserved].	3.85081e-50
NZ_CP022203.1\|WP_095961254.1\|8653455_8655072_-\|type-I-MYXAN-CRISPR-associated-Cas8a1/Cmx1	gnl\|CDD\|187844	cd09713, Cas8c_I-C, CRISPR/Cas system-associated protein Cas8c. 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; Large proteins, some contain Zn-finger domain; signature gene for I-C subtype; also known as Csx13_N family.	5.67157e-130
NZ_CP022203.1\|WP_095961255.1\|8655056_8657294_-\|CRISPR-associated-helicase/endonuclease-Cas3	gnl\|CDD\|350688	cd17930, DEXHc_cas3, DEXH/Q-box helicase domain of Cas3. CRISPR-associated (Cas) 3 is a nuclease-helicase responsible for degradation of dsDNA. The two enzymatic units of Cas3, a histidine-aspartate (HD) nuclease and a Superfamily 2 (SF2) helicase, may be expressed from separate genes as Cas3' (SF2 helicase) and Cas3'' (HD nuclease) or may be fused as a single HD-SF2 polypeptide. The nucleolytic activity of most Cas3 enzymes is transition metal ion-dependent. Cas3 is a member of the DEAD-like helicase superfamily, a diverse family of proteins involved in ATP-dependent RNA or DNA unwinding. This domain contains the ATP-binding region.	2.03186e-39
NZ_CP022203.1\|WP_157770498.1\|8636297_8637185_-\|AHH-domain-containing-protein	gnl\|CDD\|379603	pfam14412, AHH, A nuclease family of the HNH/ENDO VII superfamily with conserved AHH. AHH is a predicted nuclease of the HNH/ENDO VII superfamily of the treble clef fold. The name is derived from the conserved motif, AHH. It is found in bacterial polymorphic toxin systems and functions as a toxin module. Like WHH and LHH, the AHH nuclease contains 4 conserved histidines of which, the first one is predicted to bind a metal-ion and the other three ones are involved in activation of a water molecule for hydrolysis.	4.66714e-05
NZ_CP022203.1\|WP_095961256.1\|8657290_8657902_-\|type-I-MYXAN-CRISPR-associated-protein-Cas6/Cmx6	gnl\|CDD\|274308	TIGR02807, hypothetical_protein_LA_3189, CRISPR-associated protein Cas6, subtype MYXAN. Members of this protein family resemble the Cas6 proteins described by TIGR01877 in having a C-terminal motif GXGXXXXXGXG, where the single X of each GXG is hydrophobic and the spacer XXXXX has at least one Lys or Arg. Examples are found in cas gene operons of CRISPR regions in Anabaena variabilis ATCC 29413, Leptospira interrogans, Gemmata obscuriglobus UQM 2246, and twice in Myxococcus xanthus DK 1622. Oddly, an orphan member is found in Thiobacillus denitrificans ATCC 25259, whose genome does not seem to contain other evidence of CRISPR repeats or cas genes.	3.22589e-87
NZ_CP022203.1\|WP_095961251.1\|8650170_8651832_-\|type-I-MYXAN-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274899	TIGR03983, hypothetical_protein_LA3181, CRISPR-associated endonuclease Cas1, subtype MYXAN. Members of this protein are the Cas1 endonuclease, or Cas1 domain in Cas4/Cas1 fusion proteins, of the MYXAN subtype of CRISPR/Cas systems. These systems typically feature repeats and spacers each about 36 base pairs in length. Species with this type of CRISPR system include Myxococcus xanthus, Cyanothece sp., Leptospira interrogans, Sorangium cellulosum, Anabaena variabilis ATCC 29413, etc.	0
NZ_CP022203.1\|WP_095961252.1\|8651877_8652522_-\|type-I-MYXAN-CRISPR-associated-protein-Cas5/Cmx5/DevS	gnl\|CDD\|131635	TIGR02586, CRISPR-associated_protein_Cas5, CRISPR-associated protein Cas5/DevS, subtype MYXAN. This model represents DevS of Myxococcus xanthus and related proteins of Leptospira interrogans and Gemmata obscuriglobus. This protein is encoded in a cluster of CRISPR-associated (cas) genes, and in the special case of Myxococcus xanthus has taken on a role in the control of fruiting body development. CRISPRs are clustered, regularly interspaced short palidromic repeats. This protein family is related to models TIGR01868, TIGR01895, and TIGR01876.	1.79288e-92

>NZ_CP022203.1|WP_095961673.1|8647756_8648905_+|IS4-family-transposase
MSKSITHAEVHRFIEEAVGPDTHAKRVLSLSNATLGAVHAASLSVRAIGLALSQARGLEGKHAIKQVDRLLSNSGVDVWRLFAQWVPFVVAERKAVTVTIDWTDFESDDHTTVAIQLVTRHGRATPLLWKTVPKSELAGQRNAHEDALLERLHQVLPSDVEVTVLADRGFGDVALYELLDRLSFGYVIRFRGVVHVESAGGEVHKAKEWVPPTGRPKLLRGARVTQARFGVGAVVCVHQKGMKEAWFLAASSKEATATELVKAYGRRFTCEETHRDIKDLRFGMGLSAIAIGTCERRDRLLLLSAFAMALLTLLGAAGEATGLDRKFRADTRKTREYSLFRQGIIYYGALANMREEWLRPLMEKFAELIREQAVFREAFGFI
>NZ_CP022203.1|WP_095961249.1|8642143_8642875_+|hypothetical-protein
MTERPVPEGYYAGAYWGPRKESPEECAQRAANFLNLLAPHDPLLAHWYKPARSAKDARKHPLMPPDVPTLTGLFRRGVNRERGGPAIEQLGYTLWFDNGGGKFDRAGLQILCGCYSEAVSNACVLTLPSTGPEAERVGAVPVLAGAVRSMAMTWDPDWAVATSDSFRRLMREPSKSSAFVGWVTYLSRRRGMVPPLPAPVRIEPVEDKGTLIILTPERLTARNPEHVEQGRRVCELLARAGRM
>NZ_CP022203.1|WP_095961248.1|8640508_8642131_+|hypothetical-protein
MRANALLLFVAVLATGCASLTPAPGRGRSLSYTTRGATAPPLAPSPSEEYPHAPASLPPSVAGPEVPERLSRRRGFREVATGASPGSVAGAVGGFVARGTAQEDAWEKLLTDAGLEERDERPMGGALSPTQAARLLGVLLRRPVTLGTFPPRMAVGYLLREVLEEGEVSRDELLRRVERFARVAVLRPDGYLAWTRTGRTQQKAAPVEWRDGAFRAGPFELGRFYVSNGFVFQLADERLAPVEGSVFVEVYDDADYVGRTLDGAEAAFVKLALSIGHFFTYPLDSIASLKNLPAGVAALIESSPEYFERFRYMTRGEQVQAIAELATNLLVTTGTATGTTRTITGALAGAEATVPVLSLSARGALAIERVAVPVGRAAAVLGGGPGATLILHRANTAAPGAGPSKGPGQWGPAKESMKPPARRYQEQITGHGADEAYWVGGMSAAEGGVKFDGFKDGVLLEAKGPNYANKFEDSLEPRFWFANSGAAEMVKQAQRQIESVRGMGIPIEWHVAEAKVAEAIELLFERNQVSEIRVVHTPPL
>NZ_CP022203.1|WP_095961795.1|8639307_8640519_+|hypothetical-protein
MTRLEAATLALLPRAGAGEREGFVQVEPTVILDGGPEFGLNVGAPVRLRLWGGAAGASVVRREDWDSLSDWGQLVRGLKFGSDTAPLGVWFGALEGYSLLTGHLVRRYSNRMNPDYHPAGGVLTGTVGPLYTEAFVSDVLGARLMGAELSLDMQHVLFGKPKEKGRYTLALSAVHDWGKVGGRAPSVTLAHLDATAVVLVRPGFEALVVAGWGGRPIEGGAWGAVAGVGADAVTPTLDMTLRLEVRRQHGGFRQGFFGPDYELARFHAAGPEGVPLAEAAFPEGFSLYGEAAVGWDAVSYGGRYRHLQLSLGAEAFTWGRFDVDGRVAVQLFERSLEVALKGLGVGMGQPGARYLGAAEVRWRVLRGRLYALGTGGTLLFPQGDGTLRPGAFASVGLGVEHAR
>NZ_CP022203.1|WP_095961246.1|8637773_8638235_-|DUF4150-domain-containing-protein
MANTVGVNKMSVVTKDSKGVTVAFPDVCKTPGPAGPVPIPYPNVARSADTEQGSKKVSVEGNPVCVRDSNFSTSTGDEAGSVGGVVSGTTRGKAEFVNFSFDVQFEGKSVARAFDLMLHNDRNTPPTPLMQPPVAGLGVPPEKRPCDTCGKER
>NZ_CP022203.1|WP_095961245.1|8637254_8637728_-|hypothetical-protein
MVSEEPILAPRVGWVAGASADGALWVDFKGNRRGPLLARTTVVLASEVIRRASVARQGALLLFENGDPSLPVLVGLLQRSLSAPLTEALLDSLGAGPREARVDGKQVRLEAREEVTLKCGKASLTLRRNGDVILRGVNIQTEAEQVQRIKGGKVQVN
>NZ_CP022203.1|WP_157770498.1|8636297_8637185_-|AHH-domain-containing-protein
MVNMPRTSTRKRTVKKAPLRTKVRKRHSVGGAADKKGTAVKKPKPPPSPHSWEGSYISDDHAHGCVNRHISAYTPSNPCSHRHQARLKAQQNPAKYTWPADADRQPDTVGAWDLTADGNFETHARTPFYHEAHHIVANAELQAVVAEAGEGIEPRGRVPLIVRSGLMREGYNLNSQLNMIILPMVKYAAVALGLPLHRRTPLHFHHAIYSEYIKRELRKRFSWVKKAAAEHEVPEYQATREAVELLSMEVQPQIIAAGEAMKAGTMAGDALEDIPHEFLSGGRNKGVDMLTGPPP
>NZ_CP022203.1|WP_095961243.1|8634324_8635668_-|TIGR02270-family-protein
MNTALRPSAARTAPRRPPLLWDVLTEHLEEASFLWAQRARAMGASDFTLSEVEAGDEARLRAHLDGLRVGGPPVALRLLRPALEDDEPGRVVSAASVLLAAGEQALVLARWEEDGARRPWLGHALALGEPPALDAALLELLPRLAPALQAELLDVLAFRQVDAGPLLERLALADTEPALLAAAFRAARVTQPPVLAAWLRKGLEDPRPRVRDAAIEAGLLRGLRAAWQSCQALATEGPEPRLAMLALAVGGGHADVERLVRTLDRPERRAEALWALGFSGRMAAAEAALEVLKARAPEVAWLALRTFSVITGLPPEDLFIRAEDEDEDEVASPSEAVSSLLPPPEHRSGQVRVAEVARWWAQARERFDPEGRYRAGAPWTPEALLQALHLAPMRHRPALAFELAVRSRGACQVEPRGWCGHQRARLRAARARSLERLTRGFDGWMIS
>NZ_CP022203.1|WP_157770497.1|8633200_8634328_-|hypothetical-protein
MSAPREAPPRDVLGVITAIGAVTSVGRGAAASCAAIRAGISRPRRVSHFQVLEPETQDTVPLTAHPIQGYTDGFVGMGRWLRLARGCLGEVLETPGLPRPSDARFWDRAGLLMVIPSRDDGLFELEGDDGLEGIREDCLRPLLDALGLALPDAKVWVVDQGPAGTATAVQQASGELWRAGFERVLVLAVDSLVDPEALRMLDEEGRLKVGDNPVGLMPGEAGACFLLEQEEAVRRRGAAPLALVTGVATAEERLHLYAGHVSQGAGLAACLREVLARGPVPARFEGDLYSDLNGEEWRAREWGTALVRLGDALGAHGVQLPCVSVGDVGAASGALGVCLSVHAFTRGHSRTAQSLVVSSSPWGAVGCLRLHSTGA
>NZ_CP022203.1|WP_157770496.1|8632398_8633166_-|immunity-49-family-protein
MASRFLPAVIENALHQNRALRRVLVRRAGSARHILTFCDNLRLAGIGALFLTGTSEPFLQRLQQSGRAFAHHLREVGSADLRLSRSRPLFDAVGAGDFHGAALIAQRARRTWTQGEEYEEDFLFVEFVIQHGVLDAPVAACEDLLMRYERALRGAEDLRFDVCRALLQADSEGFNQALGVFLSERKDRLEAQARTAPFPEEFLATEWSFSLEGLALVRLAERNGLETEEDYLHIPSLAREPHRTPLGEDAWMDAD
>NZ_CP022203.1|WP_095961250.1|8649873_8650167_-|CRISPR-associated-endonuclease-Cas2
MAEPRRWYLITYDIRDPKRWRKVHGLLKGYGEWLQLSVFRCSLTDRDREKLRWELSRRMDAVDTLLVIGLCGGCVERVRAINAKEDWPEEPAPFKVL
>NZ_CP022203.1|WP_095961251.1|8650170_8651832_-|type-I-MYXAN-CRISPR-associated-endonuclease-Cas1
MNVPVTSPKPDVAEPSIRTHALHALAYCERLFYLEEVEELRVADASVFAGRRLHVQLQEEGERVELELASEALGLHGRVDALRTREGTLVVHEHKRGRHAPGRDAPEAWPSDRLQAGAYALLVEERFPGTPVECRVRYHQTDTTVSFPLDAALRRDVAAAVSRARLLRASRERPPVTPEERKCAKCSLAPVCLPEEERSGAGEERPRLFPEDDVRLVLHVTTPGARVGKSSEQLVVTPPDGEGEPTRQPGRMVSALIAHGAVQVSAQALAYCVENDIGVHWFTSGGRYLGGLTGGAGSVHRRLRQFEALRQEAVCLGLARRLVAAKLEGQLRFLMRASRGDTESRKVLASAVRDLRELLPKCAEAPSLEVLLGLEGAGAARYFGALPYLQGEDVDARLRFDGRNRRPPRDRFNAALGFLYGLVHREVEAAIRAVGLDVAFGFYHQPRGSAGPLGLDVMELFRVPLADMPLVASVNRRAWDADADFEVTSEHVWLSKTGRAKAIELYERRKRETWKHNVLGYSLSYARLVELEVRLLEKEWTGKPGLFATFRLR
>NZ_CP022203.1|WP_095961252.1|8651877_8652522_-|type-I-MYXAN-CRISPR-associated-protein-Cas5/Cmx5/DevS
MIALELSVPVACWRKGRARELVETEVLPPPATCYGALLSLVGEQDRERHRGCRVTAGVLNAPVISTVLRTFWRSKNLKVAKGNDENAAPDQQQLVIEARLVVWCDSGEEVDSRESLEVRVIRAMLEPGTVTRSGAWSLGESTHLINDAHLLPAGRPPASCRTFLVAPAGALTLPVWVDHVGTRGSRYAVGLLEDVLEAPAVQRLPRIPLAEGAG
>NZ_CP022203.1|WP_095961253.1|8652518_8653427_-|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR
MSLHVFAAFVTPLGTAANNRGLTEGNITSLQKLVWNGQVHTTVSAESIRFALRRRLNALEPCNRTYDDALRANEWKDKDFSAWAAKSKEKTYIDDDLLGFMAAEGAKQEGDKGTAKVRRAVLEVSRAVSLTPWSGDVTFNAASPGATPSAQKKGSNPVPYGTEMHATRYQYGVALTPDALRVPARAVTALNQLCALGPVAGNHGRFLFDFSPESVVFRLTQEAAPRILYAFEPSSRPGGVELAALLRKVKSGDVPAKELVLGGQAVEGLSAEEREVLSGAELHAGVVAACRAACKRMEAGKR
>NZ_CP022203.1|WP_095961254.1|8653455_8655072_-|type-I-MYXAN-CRISPR-associated-Cas8a1/Cmx1
MAKAVSSRKKALPAPLTVRLYAPGMTPLLRAGAGGLAASLRAILGDAAPWPAPVPLGPGTATVAPEAIHLDWGGEPPEATLRALFGASFQVRQGFIDLPGTRAPGAPEPPPALAAALHDALKVTFLQHGKSTQGGARRRVTFEVDAQPVVVESQGYESFVHQTAWRDVLKALESGTTSLASWAYPGAAERHLGVRVTKVEYTAAEALCACFALVGCVSYKLPQLRGGAFVALAPTDLVRFAELRPRLTPMRLHDVAVAGAADAVLAAQLVLAQESGKRRLGAVLGTTEAVALRQMPWNAQQKIRGAVVRQDAVREAVLDRYEAAAAALPHTLRVRKPEGKAKGDAGYFIATSALRAFITENLAAARPWYAGFATATTAEGRFIHTYRDRDNLGALLWHERKGLTTMHSYLGDAEQWLVQSVHLALRARFRSIYKDTEHSPKATRSNRLKGERERLRLGFAGAKTPEQVRAALADLWSRAGSNSELQEHWREVLPLLGPERWREARDLALVALASYQSQGPEAAELESADDESAADEQS
>NZ_CP022203.1|WP_095961255.1|8655056_8657294_-|CRISPR-associated-helicase/endonuclease-Cas3
MKRLLAKSTATPDRPEGEATLLGHTALVLSAARRLLEHRGRASLLAAGLDPALEPRLRRIVLLAAALHDLGKCSEHFQSMLRRKRDAPQWVRHEALSLWLCWPGQPLSAWLLRDVSELDLGLALVCVAAHHRKFQADAFAPEDAGAGLTVELLVQHEDFTRTLARIAEELSLSAPPVFTAPLLLRATRTAHPRDQLQAWQEDFERTIPASAMDARLLAVCKALVLAADVAGSALPRSGERQDWVDRQLTAPHPGEALLAVVERRLAGRMPRPFQEAVARCAAPLTLVRAGCGSGKTAAAYLWAARQHPGRPLWLTYPTMGTATEGFRDYLHGADVDARLQHSRAEVDFDIFGLRDGAARELGSREQDRLDALRSWGVDAMSCTADTVLGLVQSQRQGLYAWPALCAACVVFDEVHAYDDRLFGCLLRFLEALPGIPALLMTASLPAARLGALREVCERVHGQRLAEVDGPEDLEALPRYQRLDVAEPWALVARCLEGNGKVLWVSNTVERCMRTAEVATSHGAHALLYHSRFRYADRVHRHGDVIETFATPDRAVFASTTQVAEMSLDLSADLLVTDLAPIAALIQRLGRLNRRSTPERPGPVRPFVVLPFDGPPYGAPDLREARAWLERLGTDPLSQQDLVDAWSPSTVASPRRASSTWLDGRFDTWPAPCRDGSPSLTVLLEKDAEDVRTGAVSAHKVTLPMNLPPDSFRWRAWPRAGRLPYPIPPAHLLEYDELRGARWRKP
>NZ_CP022203.1|WP_095961256.1|8657290_8657902_-|type-I-MYXAN-CRISPR-associated-protein-Cas6/Cmx6
MALIDLLFPVQGGPVPLDHAYLLFAALSRHIPALHERSDLGVFSLRGVSNTRELLYLGRGTLRLRCPVEAVATLLPLVSAPLEVAGRRLSLGAPSLYALEPVPSLAARLVTFKHAMDEPAFIAAASRALEALGVQATLTVGRRRIVRIADKKVVGFALDLHGLSAEHSLRVQERGLGGRRHMGCGLFLPPGRAALAQARGRAA
>NZ_CP022203.1|WP_095961258.1|8658314_8659784_-|SAVED-domain-containing-protein
MGEQSASRLEGDRYQHLLSWYELLRLLDAGSPFAHGYVEHPEAGSADDVTLHARPGAGAGSRYMQVKWHVDHRETYSVAGLVAPPRVGRSLLGKLLESWLSLRPQGPVEIWLLSNWASAEDLGRYLHGRDHCFTEAFFAQPARGALKRHWAEWQQRLGVPAETLRAFCKDLRLRLGVGGIADVEEQVDDRMGRLGLRMGRQPRAIAVDGLREWIEVGGGRKHVTAESLREALREWGLVASREDAPEVSLWIHGWARRVWERPPTEELDWTPHFDRDTRKVPSEAAWRDVLLPSLLAAKQRLSRRPDGALIDLRGKLPLSTVLAVGFHLPEVGGYRFRVEQPTRGETFLWRSDTKPSERRLRVTGHEGKADATGLLVVFQLTGDARADMERFMAERPGHFRAVLYLEPEDGPHDGAVGSDADAVAFAVQAREQLRRARNELRTGVTHLILYAPAACCLFLGQRLNAVGPVVAYERTGAGGYAPALTLETG
>NZ_CP022203.1|WP_095961259.1|8660109_8661033_+|DUF2381-family-protein
MFPPGSLVMAAVVLLLGTAAVAQTPNTKRWRRIERALVLSAGAGEPVQRLRLAPGVVTTVLLDSGAVLEGELPEALRGLFSRLDVTGTHLLLQPTVVMPAQGVPPLVLRFTDAAAPQRLVLELTTEANVVDSVVDVRRHPATVAQLEAELVALRERNALLEARLATARRQAPHPGLAGAILSGAIGITGVLETWLDAPASEAELKVRQLNSYRSGSWVAVAVKLENPPGDVPWQPGIARLTSLDSNGQPTDEPMELPLLLKEPRLLPGQSAVAVVQWPVPSRPPAAYALELWDTGRRRGARWARLKP
>NZ_CP022203.1|WP_095961260.1|8661063_8662920_+|serine/threonine-protein-kinase
MRLESNASSPGPLVLSPQALPVGTRVERWRVERRIGGGGNGTVYEVRSRPEGRSYALKLAHAPDDPRFQREARTLRLLRHPGVVRLQATGTWRAGATAYPYLVMEHVRGRTLYDWSRARNPTARHVASLLAQAAWALDAAHRRQVLHRDFKGENLRVEEHGRLVVLDWGAGWHPRAAPITSAARLPPGTGPYRSPQAILWSMRAPRQTACSEHYPYTVEDELYSVGVTFYRLVVEQYPPLVLDKAHAPAISATVRALNPRVPEPLARWIERLLAFAPEARPRGAGYLAREVQHAQAHGGPDWDVPLFGWYEGPSTATRTTQEEDPWGPVAPGEEAALLQARALREARVQHHRLSRWLRRRIRSEVQTQPRTEPASPPEPRPKGRWMRAAGGLTLVACMAWGLMLAGPPHTAPAPSQPVQQLARPRGPTDTGAPATALPFSTAAPPWPGNAMPTTEPHARCIPRLHRYILAAFTAAHLNACSGPQVRPEPARCPSEALEAMSQLGLDLRSHGPIQFDIQQPDDSYQTNYSIVVSDGPITSRLDEPMGRLPANTLFYGRIWTGGEKIQGRYTLARTPDGSEYPVCFILGNETGMSKYRGSRPGHTRAHPWSNAQVVHHFP

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Crispr_ID: NZ_CP022203_18

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_18

8678532-8683018

TypeIII

I-A,I-B,II-B

Consensus_repeat	Method
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	PILER-CR
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CRISPRCasFinder
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CRT

62 spacers

cmr6gr7,cmr5gr11,cmr4gr7,cmr3gr5,cas10,cmr1gr7

The CRISPR arrays of NZ_CP022203_18

>merge|NZ_CP022203|18|8678532-8683018|PILER-CR,CRISPRCasFinder,CRT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACATGAGTTTCAGCGCACCGACTGGCGCGCAGGGAACGTGCTCAACGCCTTCCGGCATCACGGCGAGCAGGACCACGTGCTGATGGGGGAGCGCAGCGCGCGCCAGTTCCAGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGGTGGGATGCCCGTGGCAAAGAAGGTGCATCAGACGGCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCACGCTGTCGAACGTCGCCAACACCGTCAACACGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGAGGCGTCGGTTTGCGTAGCGCGCCCGAGCTCGACGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGCGCTTCGGCCTCTCGGTAGGCCCGGAGGGCGGCGGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCCTCTACGACGTCCAAGGGACGCAGGGGCAGGAGTAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGGTGTGGCACTTGATGGACTATGTGAAAGAGCCTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGTGGCCGCCCGCGCCTGTACTGCCACGACTGCGGACGTCTCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCCGCCGCCCGCGCGAGGCGAATAGGTGCGGACGTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACACAAGAGACGAGGGTACGCGAACAGGAGTAAGTCCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACACTTCTGGGCACCATGGTCGCCTGGGGGCTCGACAAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGAACGAATCTCCCCGAGGTGGGCGTGGCGCGCGAGCGCGTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGAAAAAGGCCTTCCGTCACCCCAACCCCGATTTCTAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCGGAGGCATCCGTCTTCCCAGCCGTGTGGTGGAGAATGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTGAACCCCCCATCACCTCCAAGCAGCTGGACCAGGAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGCCAGGTACGCCCAGGCGTCGTCCGACATCAAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTCGCACAGAGGCCTCGGGCACGCGCGGGGCCAGGAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACACCCGGGTGCCACGTCATGACAACGTGGCGGCGGGAGTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCAGCATCCGCAGCACCTTCTCCCAGCGCTGGCGCTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCACGTACAACGAAGAGATTGGGGACTCGCTCAAGACAGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTCTTCATCCATGCCTGGTACGACTTCGCTTCGACGTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGCGGACCTCCAGAGGGCCCTCCGGGCGAACCCCGCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGACTGGGCCTGCCGGTGCAAATCGGCCAGGGCGGACGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGGCAGAACCCGACGGTGACGAAGGCGGACGTGGAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCGTCGATGTCCTGCTGCCCATCCCGGATGAACAGGTGCTCAACACCTTCCGGCATCACGGCGAGCGGGACAAACCGAAATGCCGATTCAGACTTCCGTTGCCGACGTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGGCGGGTGAAGTCCGGGCCGTTGTCCACCTGCAGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACACGCCGCACCTGTGACGGTGACAGTCTGCGCTGCCTCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCTCCAGCAGGACACGCATGGCGACATCTGGGGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCCAGAGCAGTTGTAGCCGCTCGACTCCGTGGAGACGATTACGGGTGCTCAACGCCTTCCTGCATCACGGCGAGCGGGACTTCCGTCTTTTCGATTCGTTCAAGTTCGGCGTCCAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGTGCCCTCCACGTCGTAGCCCTCGGCCTCGGCGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGGCGATGGGGCCGCCCAATGGGAGGCAGTCATGGAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCTGCTCGCTGCGCCGGTCATCCGGAGGCGATTCCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACACCTTCTAGGACCTCCAGCCATGACCGACGACAACCCCTTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACATCGAACGGGCGGAGAGCTTGACCACCGCCCGCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCAGCGACTACGACGGACGCCAGCCCCGTTGAAAGGCCAGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCTTCGCACCGAAGGGCAAGGGCAGGCCCAGAGTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCCAGGACACGGTGGCCGGCATCGTCTTCCTTGGCAACGCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCACTTCGGGGGCGGAGGGCTGGGCCTTGAGCGGCGGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACACGCCCGCCGAACACAAGATGGCGGAGGTCTTCAGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACAGACTTGCGGCAGCCCGGACAAGTCGAGCGGCTGCCCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACATGTCCCGGATTTCCCAGAAGTGAGCCATGATGTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGGCCCTGTTGACCCGCCCCGCCGCCTACCGCCTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACAAGGGCGCCTGTCTGACGCTGGTGGGCCTGCTGCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGGCAAACCCATCCGTACTCGTCGAGCTAAGCGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGTACGGCTGGCATGGGCCTCAACCTGTCGAGGGCCGAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGAATCCGAGAGGACGCGCCGAACATCGAGTCGTTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGGGAGGCGCTACGCGGGCTGGACGTCCGTCCGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACAAGGGCGCGAGGGAGGGCAACGAGGACAGGCGCGGGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCGCTGGGCGCGTGGCGCGTTCGACTCGCGGGTTTCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGGTAGGCGCGTCGCCGGTTGAGGCGCTGATGTCGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGGCTACGCTGGGACGCCGTGCGCGCCCGCTGGGGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACAACGAACTCAAGATGCCTGGGCATGGAGTCATGTATAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTGGTGTCATCGCTGATGATGACCTCGTCGCGCTTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCAGAGACGGCTCTAGACATCGGTCGCGGCGAGACGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCGCGAGCGTGGTCCCTGGGCTGTCTGGATGGAAAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGGGCCTGGGCGCACGTCGAGGCAGACACGCCGCTGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCTCCGTGGCGGGCGGAGCGTTGTCCGCTCGCGAGGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGGTGCCCTCAGTGGACGGCAGCGCCCATGTTGTAGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGCCTGCGGCGCACGGGGCGTTTGCGGCGGGGAGGTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC

>NZ_CP022203|18|5|8678532-8683018|PILER-CR
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ATGAGTTTCAGCGCACCGACTGGCGCGCAGGGAAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCAGGAC	CACGTGCTGATGGGGGAGCGCAGCGCGCGCCAGTTCCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGTGGGATGCCCGTGGCAAAGAAGGTGCATCAGACGGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CACGCTGTCGAACGTCGCCAACACCGTCAACAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GAGGCGTCGGTTTGCGTAGCGCGCCCGAGCTCGAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGCGCTTCGGCCTCTCGGTAGGCCCGGAGGGCGGCGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCTCTACGACGTCCAAGGGACGCAGGGGCAGGAGTA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGTGTGGCACTTGATGGACTATGTGAAAGAGCCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GTGGCCGCCCGCGCCTGTACTGCCACGACTGCGGACGTCTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCGCCGCCCGCGCGAGGCGAATAGGTGCGGACGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACAAGAGACGAGGGTACGCGAACAGGAGTAAGTCC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACTTCTGGGCACCATGGTCGCCTGGGGGCTCGACAA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGAAC	GAATCTCCCCGAGGTGGGCGTGGCGCGCGAGCGCGTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGA	AAAAGGCCTTCCGTCACCCCAACCCCGATTTCTAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCG	GAGGCATCCGTCTTCCCAGCCGTGTGGTGGAGAATGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTG	AACCCCCCATCACCTCCAAGCAGCTGGACCAGGAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGC	CAGGTACGCCCAGGCGTCGTCCGACATCAAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTC	GCACAGAGGCCTCGGGCACGCGCGGGGCCAGGAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACACC	CGGGTGCCACGTCATGACAACGTGGCGGCGGGAGTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCAG	CATCCGCAGCACCTTCTCCCAGCGCTGGCGCTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCAC	GTACAACGAAGAGATTGGGGACTCGCTCAAGACAGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTC	TTCATCCATGCCTGGTACGACTTCGCTTCGACGTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGC	GGACCTCCAGAGGGCCCTCCGGGCGAACCCCGCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGAC	TGGGCCTGCCGGTGCAAATCGGCCAGGGCGGACGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGG	CAGAACCCGACGGTGACGAAGGCGGACGTGGAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCG	TCGATGTCCTGCTGCCCATCCCGGATGAACAGGTG
CTCAACACCTTCCGGCATCACGGCGAGCGGGACAAA	CCGAAATGCCGATTCAGACTTCCGTTGCCGACGTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGGC	GGGTGAAGTCCGGGCCGTTGTCCACCTGCAGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACACG	CCGCACCTGTGACGGTGACAGTCTGCGCTGCCTCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCT	CCAGCAGGACACGCATGGCGACATCTGGGGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCC	AGAGCAGTTGTAGCCGCTCGACTCCGTGGAGACGATTACGGGTG
CTCAACGCCTTCCTGCATCACGGCGAGCGGGACTTC	CGTCTTTTCGATTCGTTCAAGTTCGGCGTCCAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGTG	CCCTCCACGTCGTAGCCCTCGGCCTCGGCGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGG	CGATGGGGCCGCCCAATGGGAGGCAGTCATGGAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCT	GCTCGCTGCGCCGGTCATCCGGAGGCGATTCCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACACC	TTCTAGGACCTCCAGCCATGACCGACGACAACCCCTTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACATC	GAACGGGCGGAGAGCTTGACCACCGCCCGCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCA	GCGACTACGACGGACGCCAGCCCCGTTGAAAGGCCAGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCT	TCGCACCGAAGGGCAAGGGCAGGCCCAGAGTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCCA	GGACACGGTGGCCGGCATCGTCTTCCTTGGCAACGCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCAC	TTCGGGGGCGGAGGGCTGGGCCTTGAGCGGCGGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACACG	CCCGCCGAACACAAGATGGCGGAGGTCTTCAGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACAGA	CTTGCGGCAGCCCGGACAAGTCGAGCGGCTGCCCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACATG	TCCCGGATTTCCCAGAAGTGAGCCATGATGTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGG	CCCTGTTGACCCGCCCCGCCGCCTACCGCCTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACAAG	GGCGCCTGTCTGACGCTGGTGGGCCTGCTGCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGGC	AAACCCATCCGTACTCGTCGAGCTAAGCGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGTA	CGGCTGGCATGGGCCTCAACCTGTCGAGGGCCGAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGAA	TCCGAGAGGACGCGCCGAACATCGAGTCGTTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGG	GAGGCGCTACGCGGGCTGGACGTCCGTCCGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACAAG	GGCGCGAGGGAGGGCAACGAGGACAGGCGCGGGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCG	CTGGGCGCGTGGCGCGTTCGACTCGCGGGTTTCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGG	TAGGCGCGTCGCCGGTTGAGGCGCTGATGTCGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGGC	TACGCTGGGACGCCGTGCGCGCCCGCTGGGGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACAAC	GAACTCAAGATGCCTGGGCATGGAGTCATGTATAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTTG	GTGTCATCGCTGATGATGACCTCGTCGCGCTTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACGCA	GAGACGGCTCTAGACATCGGTCGCGGCGAGACGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTCG	CGAGCGTGGTCCCTGGGCTGTCTGGATGGAAAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGG	GCCTGGGCGCACGTCGAGGCAGACACGCCGCTGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCTC	CGTGGCGGGCGGAGCGTTGTCCGCTCGCGAGGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACCGG	TGCCCTCAGTGGACGGCAGCGCCCATGTTGTAGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGACTGC	CTGCGGCGCACGGGGCGTTTGCGGCGGGGAGGTG
CTCAACGCCTTCCGGCATCACGGCGAGCGGGAC

>NZ_CP022203|18|12|8678532-8683018|CRISPRCasFinder
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ATGAGTTTCAGCGCACCGACTGGCGCGCAGGGAAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCAGGAC	CACGTGCTGATGGGGGAGCGCAGCGCGCGCCAGTTCCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGTGGGATGCCCGTGGCAAAGAAGGTGCATCAGACGGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CACGCTGTCGAACGTCGCCAACACCGTCAACAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GAGGCGTCGGTTTGCGTAGCGCGCCCGAGCTCGAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGCGCTTCGGCCTCTCGGTAGGCCCGGAGGGCGGCGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCTCTACGACGTCCAAGGGACGCAGGGGCAGGAGTA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGTGTGGCACTTGATGGACTATGTGAAAGAGCCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GTGGCCGCCCGCGCCTGTACTGCCACGACTGCGGACGTCTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCGCCGCCCGCGCGAGGCGAATAGGTGCGGACGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACAAGAGACGAGGGTACGCGAACAGGAGTAAGTCC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACTTCTGGGCACCATGGTCGCCTGGGGGCTCGACAA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGAAC	GAATCTCCCCGAGGTGGGCGTGGCGCGCGAGCGCGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGAAAAAGGCCTTCCGTCACCCCAACCCCGATTTCTA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCGGAGGCATCCGTCTTCCCAGCCGTGTGGTGGAGAAT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTGAACCCCCCATCACCTCCAAGCAGCTGGACCAGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGCCAGGTACGCCCAGGCGTCGTCCGACATCAA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTCGCACAGAGGCCTCGGGCACGCGCGGGGCCAGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACCCGGGTGCCACGTCATGACAACGTGGCGGCGGGAGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CAGCATCCGCAGCACCTTCTCCCAGCGCTGGCGCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CACGTACAACGAAGAGATTGGGGACTCGCTCAAGACAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTCTTCATCCATGCCTGGTACGACTTCGCTTCGACGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGCGGACCTCCAGAGGGCCCTCCGGGCGAACCCCGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GACTGGGCCTGCCGGTGCAAATCGGCCAGGGCGGACG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGCAGAACCCGACGGTGACGAAGGCGGACGTGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCGTCGATGTCCTGCTGCCCATCCCGGATGAACAG
GTGCTCAACACCTTCCGGCATCACGGCGAGCGGGAC	AAACCGAAATGCCGATTCAGACTTCCGTTGCCGACGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGCGGGTGAAGTCCGGGCCGTTGTCCACCTGCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACGCCGCACCTGTGACGGTGACAGTCTGCGCTGCCTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCTCCAGCAGGACACGCATGGCGACATCTGGGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCCAGAGCAGTTGTAGCCGCTCGACTCCGTGGAGACGATTACGG
GTGCTCAACGCCTTCCTGCATCACGGCGAGCGGGAC	TTCCGTCTTTTCGATTCGTTCAAGTTCGGCGTCCA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GTGCCCTCCACGTCGTAGCCCTCGGCCTCGGCG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGGCGATGGGGCCGCCCAATGGGAGGCAGTCATGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCTGCTCGCTGCGCCGGTCATCCGGAGGCGATTCC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACCTTCTAGGACCTCCAGCCATGACCGACGACAACCCCTT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ATCGAACGGGCGGAGAGCTTGACCACCGCCCGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCAGCGACTACGACGGACGCCAGCCCCGTTGAAAGGCCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCTTCGCACCGAAGGGCAAGGGCAGGCCCAGAGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCAGGACACGGTGGCCGGCATCGTCTTCCTTGGCAACGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CACTTCGGGGGCGGAGGGCTGGGCCTTGAGCGGCGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACGCCCGCCGAACACAAGATGGCGGAGGTCTTCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AGACTTGCGGCAGCCCGGACAAGTCGAGCGGCTGCCC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ATGTCCCGGATTTCCCAGAAGTGAGCCATGATGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGCCCTGTTGACCCGCCCCGCCGCCTACCGCCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AAGGGCGCCTGTCTGACGCTGGTGGGCCTGCTGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGCAAACCCATCCGTACTCGTCGAGCTAAGCG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GTACGGCTGGCATGGGCCTCAACCTGTCGAGGGCCGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GAATCCGAGAGGACGCGCCGAACATCGAGTCGTT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGGAGGCGCTACGCGGGCTGGACGTCCGTCCG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AAGGGCGCGAGGGAGGGCAACGAGGACAGGCGCGGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCGCTGGGCGCGTGGCGCGTTCGACTCGCGGGTTTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGTAGGCGCGTCGCCGGTTGAGGCGCTGATGTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGCTACGCTGGGACGCCGTGCGCGCCCGCTGGGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AACGAACTCAAGATGCCTGGGCATGGAGTCATGTATA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTGGTGTCATCGCTGATGATGACCTCGTCGCGCTT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCAGAGACGGCTCTAGACATCGGTCGCGGCGAGAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCGCGAGCGTGGTCCCTGGGCTGTCTGGATGGAAA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGGGCCTGGGCGCACGTCGAGGCAGACACGCCGCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CTCCGTGGCGGGCGGAGCGTTGTCCGCTCGCGAGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGGTGCCCTCAGTGGACGGCAGCGCCCATGTTGTA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGCCTGCGGCGCACGGGGCGTTTGCGGCGGGGAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC

>NZ_CP022203|18|7|8678532-8683018|CRT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ATGAGTTTCAGCGCACCGACTGGCGCGCAGGGAAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCAGGAC	CACGTGCTGATGGGGGAGCGCAGCGCGCGCCAGTTCCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGTGGGATGCCCGTGGCAAAGAAGGTGCATCAGACGGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CACGCTGTCGAACGTCGCCAACACCGTCAACAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GAGGCGTCGGTTTGCGTAGCGCGCCCGAGCTCGAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGCGCTTCGGCCTCTCGGTAGGCCCGGAGGGCGGCGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCTCTACGACGTCCAAGGGACGCAGGGGCAGGAGTA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGTGTGGCACTTGATGGACTATGTGAAAGAGCCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GTGGCCGCCCGCGCCTGTACTGCCACGACTGCGGACGTCTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCGCCGCCCGCGCGAGGCGAATAGGTGCGGACGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACAAGAGACGAGGGTACGCGAACAGGAGTAAGTCC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACTTCTGGGCACCATGGTCGCCTGGGGGCTCGACAA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGAAC	GAATCTCCCCGAGGTGGGCGTGGCGCGCGAGCGCGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGAAAAAGGCCTTCCGTCACCCCAACCCCGATTTCTA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCGGAGGCATCCGTCTTCCCAGCCGTGTGGTGGAGAAT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTGAACCCCCCATCACCTCCAAGCAGCTGGACCAGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGCCAGGTACGCCCAGGCGTCGTCCGACATCAA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTCGCACAGAGGCCTCGGGCACGCGCGGGGCCAGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACCCGGGTGCCACGTCATGACAACGTGGCGGCGGGAGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CAGCATCCGCAGCACCTTCTCCCAGCGCTGGCGCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CACGTACAACGAAGAGATTGGGGACTCGCTCAAGACAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTCTTCATCCATGCCTGGTACGACTTCGCTTCGACGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGCGGACCTCCAGAGGGCCCTCCGGGCGAACCCCGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GACTGGGCCTGCCGGTGCAAATCGGCCAGGGCGGACG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGCAGAACCCGACGGTGACGAAGGCGGACGTGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCGTCGATGTCCTGCTGCCCATCCCGGATGAACAG
GTGCTCAACACCTTCCGGCATCACGGCGAGCGGGAC	AAACCGAAATGCCGATTCAGACTTCCGTTGCCGACGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGCGGGTGAAGTCCGGGCCGTTGTCCACCTGCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACGCCGCACCTGTGACGGTGACAGTCTGCGCTGCCTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCTCCAGCAGGACACGCATGGCGACATCTGGGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCCAGAGCAGTTGTAGCCGCTCGACTCCGTGGAGACGATTACGG
GTGCTCAACGCCTTCCTGCATCACGGCGAGCGGGAC	TTCCGTCTTTTCGATTCGTTCAAGTTCGGCGTCCA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GTGCCCTCCACGTCGTAGCCCTCGGCCTCGGCG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGGCGATGGGGCCGCCCAATGGGAGGCAGTCATGGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCTGCTCGCTGCGCCGGTCATCCGGAGGCGATTCC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACCTTCTAGGACCTCCAGCCATGACCGACGACAACCCCTT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ATCGAACGGGCGGAGAGCTTGACCACCGCCCGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCAGCGACTACGACGGACGCCAGCCCCGTTGAAAGGCCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCTTCGCACCGAAGGGCAAGGGCAGGCCCAGAGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CCAGGACACGGTGGCCGGCATCGTCTTCCTTGGCAACGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CACTTCGGGGGCGGAGGGCTGGGCCTTGAGCGGCGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ACGCCCGCCGAACACAAGATGGCGGAGGTCTTCAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AGACTTGCGGCAGCCCGGACAAGTCGAGCGGCTGCCC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	ATGTCCCGGATTTCCCAGAAGTGAGCCATGATGT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGCCCTGTTGACCCGCCCCGCCGCCTACCGCCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AAGGGCGCCTGTCTGACGCTGGTGGGCCTGCTGC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGCAAACCCATCCGTACTCGTCGAGCTAAGCG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GTACGGCTGGCATGGGCCTCAACCTGTCGAGGGCCGA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GAATCCGAGAGGACGCGCCGAACATCGAGTCGTT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGGAGGCGCTACGCGGGCTGGACGTCCGTCCG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AAGGGCGCGAGGGAGGGCAACGAGGACAGGCGCGGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCGCTGGGCGCGTGGCGCGTTCGACTCGCGGGTTTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGGTAGGCGCGTCGCCGGTTGAGGCGCTGATGTC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GGCTACGCTGGGACGCCGTGCGCGCCCGCTGGGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	AACGAACTCAAGATGCCTGGGCATGGAGTCATGTATA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TTGGTGTCATCGCTGATGATGACCTCGTCGCGCTT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	GCAGAGACGGCTCTAGACATCGGTCGCGGCGAGAC
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TCGCGAGCGTGGTCCCTGGGCTGTCTGGATGGAAA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGGGCCTGGGCGCACGTCGAGGCAGACACGCCGCT
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CTCCGTGGCGGGCGGAGCGTTGTCCGCTCGCGAGG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	CGGTGCCCTCAGTGGACGGCAGCGCCCATGTTGTA
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC	TGCCTGCGGCGCACGGGGCGTTTGCGGCGGGGAG
GTGCTCAACGCCTTCCGGCATCACGGCGAGCGGGAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095961276.1\|8690395_8692225_-\|SAVED-domain-containing-protein	unknown	unknown	gnl\|CDD\|380122
NZ_CP022203.1\|WP_095961273.1\|8685811_8687023_-\|CRISPR-associated-protein-Crm3	cmr3gr5	cd09748_cmr3gr5_CAS-III-B	gnl\|CDD\|187879
NZ_CP022203.1\|WP_095961261.1\|8662935_8664126_-\|AI-2E-family-transporter	unknown	unknown	gnl\|CDD\|223701
NZ_CP022203.1\|WP_095961279.1\|8694200_8695025_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274375
NZ_CP022203.1\|WP_170114795.1\|8692326_8693247_-\|nucleotidyltransferase	unknown	unknown	gnl\|CDD\|143390
NZ_CP022203.1\|WP_095961274.1\|8687015_8688818_-\|type-III-B-CRISPR-associated-protein-Cas10/Cmr2	cas10	cls000742_cas10_CAS-III	gnl\|CDD\|274208
NZ_CP022203.1\|WP_095961266.1\|8671079_8672600_-\|VWA-domain-containing-protein	unknown	unknown	gnl\|CDD\|236815
NZ_CP022203.1\|WP_095961263.1\|8665832_8666918_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381306
NZ_CP022203.1\|WP_095961796.1\|8665331_8665730_-\|MarR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|197670
NZ_CP022203.1\|WP_095961268.1\|8675564_8676173_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961269.1\|8676461_8677571_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961275.1\|8688822_8690298_-\|CRISPR-associated-protein-Cmr1	cmr1gr7	COG1367_cmr1gr7_CAS-III-B	gnl\|CDD\|224286
NZ_CP022203.1\|WP_095961270.1\|8683412_8684450_-\|type-III-B-CRISPR-module-RAMP-protein-Cmr6	cmr6gr7	COG1604_cmr6gr7_CAS-III-B	gnl\|CDD\|187792
NZ_CP022203.1\|WP_095961271.1\|8684475_8684868_-\|type-III-B-CRISPR-module-associated-protein-Cmr5	cmr5gr11	cd09749_cmr5gr11_CAS-III-B	gnl\|CDD\|187880
NZ_CP022203.1\|WP_095961278.1\|8693343_8694201_-\|serine/threonine-protein-kinase	unknown	unknown	gnl\|CDD\|270916
NZ_CP022203.1\|WP_095961264.1\|8666949_8667936_-\|SWIM-zinc-finger-family-protein	unknown	unknown	gnl\|CDD\|226729
NZ_CP022203.1\|WP_095961265.1\|8667932_8670905_-\|DEAD/DEAH-box-helicase	unknown	unknown	gnl\|CDD\|223627
NZ_CP022203.1\|WP_095961267.1\|8672596_8674210_-\|AAA-family-ATPase	unknown	unknown	gnl\|CDD\|184118
NZ_CP022203.1\|WP_095961272.1\|8684864_8685809_-\|type-III-B-CRISPR-module-RAMP-protein-Cmr4	cmr4gr7	cd09682_cmr4gr7_CAS-III-B	gnl\|CDD\|274210
NZ_CP022203.1\|WP_095961262.1\|8664173_8665094_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_095961276.1\|8690395_8692225_-\|SAVED-domain-containing-protein	gnl\|CDD\|380122	pfam18145, SAVED, SMODS-associated and fused to various effectors sensor domain. Predicted to function as a sensor domain, sensing nucleotides or nucleotide derivatives generated by SMODS and other nucleotide synthetase domains. The sensing of ligands by SAVED is predicted to activate effectors deployed by a class of conflict systems which are reliant on the on the production and sensing of the nucleotide second messengers.	2.85476e-11
NZ_CP022203.1\|WP_095961267.1\|8672596_8674210_-\|AAA-family-ATPase	gnl\|CDD\|184118	PRK13531, PRK13531, regulatory ATPase RavA; Provisional.	5.66288e-82
NZ_CP022203.1\|WP_095961261.1\|8662935_8664126_-\|AI-2E-family-transporter	gnl\|CDD\|223701	COG0628, yhhT, Predicted permease, member of the PurR regulon [General function prediction only].	2.35253e-54
NZ_CP022203.1\|WP_095961279.1\|8694200_8695025_-\|sigma-70-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274375	TIGR02984, Sig-70_plancto1, RNA polymerase sigma-70 factor, Planctomycetaceae-specific subfamily 1. This group of sigma factors are members of the sigma-70 family (TIGR02937) and are apparently found only in the Planctomycetaceae family including the genuses Gemmata and Pirellula (in which seven sequences are found).	7.25848e-23
NZ_CP022203.1\|WP_170114795.1\|8692326_8693247_-\|nucleotidyltransferase	gnl\|CDD\|143390	cd05400, NT_2-5OAS_ClassI-CCAase, Nucleotidyltransferase (NT) domain of 2'5'-oligoadenylate (2-5A)synthetase (2-5OAS) and class I CCA-adding enzyme. In vertebrates, 2-5OASs are induced by interferon during the innate immune response to protect against RNA virus infections. In the presence of an RNA activator, 2-5OASs catalyze the oligomerization of ATP into 2-5A. 2-5A activates endoribonuclease L, which leads to degradation of the viral RNA. 2-5OASs are also implicated in cell growth control, differentiation, and apoptosis. This family includes human OAS1, -2, -3, and OASL. CCA-adding enzymes add the sequence [cytidine(C)-cytidine-adenosine (A)], one nucleotide at a time, onto the 3' end of tRNA, in a template-independent reaction. This class I group includes the archaeal Sulfolobus shibatae and Archeoglobus fulgidus CCA-adding enzymes. It belongs to the Pol beta-like NT superfamily. In the majority of enzymes in this superfamily, two carboxylates, Dx[D/E], together with a third more distal carboxylate, coordinate two divalent metal cations involved in a two-metal ion mechanism of nucleotide addition. These carboxylate residues are conserved in this family.	1.06557e-15
NZ_CP022203.1\|WP_095961272.1\|8684864_8685809_-\|type-III-B-CRISPR-module-RAMP-protein-Cmr4	gnl\|CDD\|274210	TIGR02580, putative_CRISPR-associated_protein, CRISPR type III-B/RAMP module RAMP protein Cmr4. This model represents a CRISPR-associated protein from the family that includes TM1792 of Thermotoga maritima. This family is part of the broad RAMP superfamily (pfam03787) collection of CRISPR-associated proteins. It is the fourth of a recurring set of six proteins, four of are in the RAMP superfamily, that we designate the CRISPR RAMP module.	4.2078e-66
NZ_CP022203.1\|WP_095961263.1\|8665832_8666918_+\|aldo/keto-reductase	gnl\|CDD\|381306	cd19080, AKR_AKR9A_9B, AKR9A and AKR9B families of aldo-keto reductase (AKR). The AKR9A family includes Aspergillus nidulans sterigmatocystin biosynthesis dehydrogenase StcV, Aspergillus flavus norsolorinic acid reductase (NOR), and Phanerochaete chrysosporium aryl-alcohol dehydrogenase [NADP(+)] (AAD), are founding members of aldo-keto reductase family 9 member A1-3 (AKR9A1-3), respectively. StcV may be involved in the dehydration of 5'-hydroxyaverantin to form averufin. NOR is involved in aflatoxin biosynthesis. AAD (EC1.1.1.91) is involved in lignin degradation and reduces aromatic benzaldehydes to their respective alcohols in the presence of NADP(H). The AKR9B family includes Saccharomyces cerevisiae aryl-alcohol dehydrogenases AAD14p, AAD3p, AAD4p, and AAD10p, which are founding members of aldo-keto reductase family 9 member B1-4 (AKR9B1-4), respectively.	8.71045e-170
NZ_CP022203.1\|WP_095961796.1\|8665331_8665730_-\|MarR-family-transcriptional-regulator	gnl\|CDD\|197670	smart00347, HTH_MARR, helix_turn_helix multiple antibiotic resistance protein.	6.66683e-15
NZ_CP022203.1\|WP_095961271.1\|8684475_8684868_-\|type-III-B-CRISPR-module-associated-protein-Cmr5	gnl\|CDD\|187880	cd09749, Cmr5_III-B, CRISPR/Cas system-associated protein Cmr5. 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; Small alpha-helical protein; signature gene for subtype III-B.	7.11617e-27
NZ_CP022203.1\|WP_095961278.1\|8693343_8694201_-\|serine/threonine-protein-kinase	gnl\|CDD\|270916	cd14014, STKc_PknB_like, Catalytic domain of bacterial Serine/Threonine kinases, PknB and similar proteins. STKs catalyze the transfer of the gamma-phosphoryl group from ATP to serine/threonine residues on protein substrates. This subfamily includes many bacterial eukaryotic-type STKs including Staphylococcus aureus PknB (also called PrkC or Stk1), Bacillus subtilis PrkC, and Mycobacterium tuberculosis Pkn proteins (PknB, PknD, PknE, PknF, PknL, and PknH), among others. S. aureus PknB is the only eukaryotic-type STK present in this species, although many microorganisms encode for several such proteins. It is important for the survival and pathogenesis of S. aureus as it is involved in the regulation of purine and pyrimidine biosynthesis, cell wall metabolism, autolysis, virulence, and antibiotic resistance. M. tuberculosis PknB is essential for growth and it acts on diverse substrates including proteins involved in peptidoglycan synthesis, cell division, transcription, stress responses, and metabolic regulation. B. subtilis PrkC is located at the inner membrane of endospores and functions to trigger spore germination. Bacterial STKs in this subfamily show varied domain architectures. The well-characterized members such as S. aureus and M. tuberculosis PknB, and B. subtilis PrkC, contain an N-terminal cytosolic kinase domain, a transmembrane (TM) segment, and mutliple C-terminal extracellular PASTA domains. The PknB subfamily is part of a larger superfamily that includes the catalytic domains of other protein STKs, protein tyrosine kinases, RIO kinases, aminoglycoside phosphotransferase, choline kinase, and phosphoinositide 3-kinase.	7.19047e-72
NZ_CP022203.1\|WP_095961275.1\|8688822_8690298_-\|CRISPR-associated-protein-Cmr1	gnl\|CDD\|224286	COG1367, COG1367, CRISPR system related protein, RAMP superfamily [Defense mechanisms].	1.47663e-23
NZ_CP022203.1\|WP_095961270.1\|8683412_8684450_-\|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.	1.25265e-39
NZ_CP022203.1\|WP_095961264.1\|8666949_8667936_-\|SWIM-zinc-finger-family-protein	gnl\|CDD\|226729	COG4279, COG4279, Uncharacterized conserved protein [Function unknown].	6.54017e-63
NZ_CP022203.1\|WP_095961265.1\|8667932_8670905_-\|DEAD/DEAH-box-helicase	gnl\|CDD\|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	5.13368e-130
NZ_CP022203.1\|WP_095961273.1\|8685811_8687023_-\|CRISPR-associated-protein-Crm3	gnl\|CDD\|187879	cd09748, Cmr3_III-B, CRISPR/Cas system-associated RAMP superfamily protein Cmr3. 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.	3.93686e-68
NZ_CP022203.1\|WP_095961266.1\|8671079_8672600_-\|VWA-domain-containing-protein	gnl\|CDD\|236815	PRK10997, yieM, ATPase RavA stimulator ViaA.	1.16872e-46
NZ_CP022203.1\|WP_095961274.1\|8687015_8688818_-\|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.	4.67616e-85

>NZ_CP022203.1|WP_095961269.1|8676461_8677571_-|hypothetical-protein
MSEHQVYEFVALERPLTAGQMAQLRAVSTRAEITPTRFWNEYHWGNLKADPAQLLLRYFDAHLYSANWGDRRLMLRLPREGLDVKALKACFPARGPSALTVAGANLVLDFRAGEEEPLDEEMPPGSLAALLPLRTELQRGDLRGAYLAWLAAVQSGCIAPSAKEPLVPEGLGALTGAQQALVGWLRLDEDLLAAAAHGREPREDDRRALRAWVRQLAPEQKTRWLLLAVDAPERPLGATLLRAFREAQAPAHSSPVRTVHELLALAKTQRERRERAEAEHRRKALAATEKRLQRRLATLARDEEGAWRRLERLVAASEYDEAMGLAEELWALASRAGAPSLFDTRFEALRKRQARRRGFFDRWKHRRPD
>NZ_CP022203.1|WP_095961268.1|8675564_8676173_+|hypothetical-protein
MNHYLIHLMPRENPDYCFIDKYPKELGLKSYKIAHGERLGPDYPANARVYMTDRYSGIQTPDLVENACGMLIVSKRVKEVLERTIMATVEYLPLTICNHKKRVASSDHFIVNPIGTVDCLNLKASDIVYHEDKVVAVRDFVLDPAKLEHAPPLFRVQEDSYAYIMSEQILEALRTLEPRPTNFLLELLNQVPASPASAPPAT
>NZ_CP022203.1|WP_095961267.1|8672596_8674210_-|AAA-family-ATPase
MAEALKKPPPDLAARLKALRDGLLTGLVERDVPVRLALLAALAGEHLLLIGPPGTAKSLVARRLHQAFHPATYFERLLTRFSVPEELFGPLSIKGLEEDRYERLTEAYLPRASIAFLDEIFKANSAILNALLTLLNEREFDNGARREPTPLVCAVGASNELPEGEELDALFDRFLLRCHVGPVSKDGFPALLGLRGNVGAEPPQQLRLSDADLAEVREMAALVDVPDDVVALLADLRDWCMAEGIQVSDRRWRKVVKLLQTAALTNGRDRVSIWDCWLLQHCLWNEPEQRAKVNDWYSARAGASAAMDPSRLTRIVVSWEGQLKRDQDSRSQAHDAEGNLLFKDSDGKPTTAKGGQGQARRGKSPLFLAPPKAQTESPHSYTYGDKGRIQDRTRAGKGFTRAELGPLWFQDASQDWTQFEDWSKRDAYLANKANWLMEEMDLPPLMEPTRQKAAHLDACLKELTALRSQVETYKAQLLAHIASLDADIRAHLWVTDDFAEPAARSLGGTRREVETLLGRLDKLRQGFEMLPREEAPR
>NZ_CP022203.1|WP_095961266.1|8671079_8672600_-|VWA-domain-containing-protein
MSDAFDAGALERGYAFLDDCPAELLQEVITFPVGTLPERVRGIRAWRDALLDGRLPPEGTWPPPEIAASARYTAEALGFLRFCKGQPELVDAFLRDVLASFTRQASVVRAELAARLRELEQLERQRLDAQEAQAAKRDRRARAATRIDEVTLARLRQQAEREVAARPAKEDAELLAAWGERTRAWAELSDVFGDLGELMGRGWDLSLGVLRHTGWMDLVRLRELVAQLPQLTEVVRSLGRLHVSDAEETIAETVFVPMRRLEEERREAWTRHVPAETRGIERSGELARMLPAEAVNLGHPKLRYLWHARRAERALLTYRVEGLEVERTLVERDSVESVERRSPRPKRGPIIAVIDTSGSMHGVPERVGKALVLEALRTAHAEKRRCFLYDYSGPGQVREFELSLTAEGLGRLLTFLGQSFGGGSDVAEVMARVVQRLDANDWKRADVLFVSDGEWPVPDGLPRRVAQAREQGTRFHGVQIGNRGRTGLHALCDPVHVFQDWAAVGG
>NZ_CP022203.1|WP_095961265.1|8667932_8670905_-|DEAD/DEAH-box-helicase
MPLVFLPDAETLFLWGPEPLPGSLDGLTDPGERASALLVTPEGLRECKGHNLPLVATVERLAVVGASEAESFPGSIALWTLASKLALELIARERVVPTLLRRGERIEARWAAALSAPEDAGRVAALARSMPPGAHAVPVGKGRAIWAPDALLRAFLDATTDAFVRAARGAPALPSRRASSWDERWREALTGAHRDFAPEGFAERSVVDELTRWSEPALGARDKLRACFRLEPPRADGEPFVLSFHLQSPDDPSLLVPAADVWKTRGRSLEKLGRAFRDPQESLLEALGRAARLFAPLALVLESPRPQALLLEPDTAWTFLSEGARALSDAGFGVIVPGELTSSGRRRLRLRMRVGAGTKAAGVVSGTAGLGLDALLRVDWDAVLGDQPLTAQELTLLARRKAPLVRFRGEWVAVAPDELDAIQRHLAQGPGRMALSEAVRVSLLGETRHGALPVTVLATGALEARLRQLRAGGATAQDAPRALRATLRPYQARGLHWLDTLASLGLGACLADDMGLGKTVQVLAFLLRRLEQAPDEARPTLLVAPTSVVGNWERELARFAPALRLTPHYGAERARAAGAFPLAPGAVVLTTYGLLRRDAALLAGVDWGAVVLDEAQNIKNAASATARAARALRATQRFALTGTPVENRLAELWSILEFANPGLLGPLETFRRELALPIERHGNPEAAARLRRLVGPFVLRRLKSDPAIISDLPAKNEMKVVCTLTREQASLYKAVVDEELRRIEEADGMERRGRVLALLLYTKQIANHPAQYLGESGPLPRRSGKLARVVEMLEEALSAGDKALVFTQFREMGDKLVTHLSERLGHEVLFLHGGTSRKARDEMVRRFQEGPHGPRVFVLSVKAGGTGLNLTAASHVFHYDRWWNPAVEDQATDRAYRIGQTRAVQVHKLVCAGTVEEKVDRLLEQKRQLADSVVGTGEHWVTELDTAALRELFSLSEGAVADEGEEDGDVVRARAPRQQGRTRAKKAVSR
>NZ_CP022203.1|WP_095961264.1|8666949_8667936_-|SWIM-zinc-finger-family-protein
MSDRDFWGWPSTPKRPPPAHGIKMKKAGTTWWGQRWLEALERVLGGDSGRLSRGRTYARAGRTHDLVIQRGEVTARVTGSRPKPYAISLTLKRLDDGVWEKAIAGMAGRAQYAAELLAGAMPQAIDEVFLAAGGSLFPRSRGELMTECSCPDWGDPCKHVAATHYVLGEALDHDPFLLFELRGRTKEQVLSALRAARGAGSDGEGATRRGAAKRRRAADAPAIPSVKPGKLTRAGYDAPREPLPALGFTFDVPSASGAVLRQLGAPASWSANVTPGEVLAPPVRAAAERARRIALEEPGAADAPATAPRRRSRAKPPTRRAKRKGADE
>NZ_CP022203.1|WP_095961263.1|8665832_8666918_+|aldo/keto-reductase
MPLNHYVTLGRSGLRVSPLCLGAMTFGEDLGWGSSVEESQQIIDRYLELGGNFIDTANFYTKSHSEKILGDHVGRHPARRDRLVIATKFSGNLYPGDPNGGGSGRKSIINAAEHSLRRLQTDYIDLYWLHNWDIHTPIEETMAALEDLVRAGKVRYIGVSDTPAWKIAQANVLAHFRGWSSFIGLQIEYSLLERSVEQELVPMALEFGLGITPWSPLKSGALSGKYTRANAGQLKGDRSAFLDHVLNEKTYALVDELGTIAREHGSTVARVALAWVQAQPGVSSTIIGARRLSQLEDNVGALEVKLTAEQLARLDALTKPAFGFPQSMQPMFPSIHNGGTTVNGVFAEPSGFGVQRGDTVY
>NZ_CP022203.1|WP_095961796.1|8665331_8665730_-|MarR-family-transcriptional-regulator
MDPARIWSLNHRLLMAVISSVAADLAALGLETKELFVLAEVDEHPYPAELASVLCIPKPSVTLYVKRLEAAGFLRREIDTEDLRRHRLHLTPAGRKAMQQGTALLSGAFGERLGRLSATQQAELRGLLEKMT
>NZ_CP022203.1|WP_095961262.1|8664173_8665094_-|hypothetical-protein
MKGIKLGGLFKSPSVPKSPSASGSGPNKPSAPPPVESKPTPKPGPVKDGFDAQGSKPSAGKVNAQPTPQPGKDVTSSFGANPLGYSGQNILNAYNMFPGSAPQGVALPTAQKPFVNANDSRVTLNAHQHQGNTNLSVSPAGGQGIPAHYMHYLSTGEGKFAGIQGVPLHPRPGEPTTVVTGALNGCAIHALHDTKQNNLSFLHHADYSKNGKAELDGFLSQHPNLKPAGSFTPADYSLPTGKHGLPAGATPFIHYSQGTANQPGQWTINGQLNTYKNGGTPGGRPELMRPTDLQVPFMQTVPVNVP
>NZ_CP022203.1|WP_095961261.1|8662935_8664126_-|AI-2E-family-transporter
MDSRRASSPSVHEATPAGGLRVPCAASCIGCARRMATPDTPPASWLTRGALFSGKLLVIAVAVVALVVLLARLYLIVLPSVVALLLATLLHPPVRWLSARRVPRALATLLALLVLLLVGVAGLFVLVPRIIQQVSAAGSNVQAGLNEAIDWVTWKLPVSRAQLDGLLQQGLVFLKSNAGRITTGVLAGANLAAQAVAGVLLTLTLLFFFVKDAEQIGGWLLARVSPARRETARAVGLRAWGTLSGYLRGVVIVALADAVGIGAGLAIIGVPLVLPLAALTFLGGFFPVVGATLAGGVAVLVALITNGPLDALLVLLVVLGVQQLEGNVLEPVVMGRAVPLHPVVILLAITAGGVLFGVAGAFLAVPVAAVLSAVGNELRLRNEARVLETPPSIEPP
>NZ_CP022203.1|WP_095961270.1|8683412_8684450_-|type-III-B-CRISPR-module-RAMP-protein-Cmr6
MRAALRHLVGTKPGETAHAGLVYERYAPVKAHEPGSKWEDWLSGLEAHAEPEGYSSAYRRWEDSLRQSHAVTFQARAESRLLVGHGHASPTGVGLTLHHTWGVPVVPGSSLKGVLAGYLRAVLGDGAAQARRRLFGVPGDAGARAQAGEVIFHDAQWVPGASGFLSRDVLTVHQKAWYGGEAEWPSDHDAPNPVSFLTVRPGGRFLVALSLAPAREQAPDAEALLAWAARRLDEALRHWGVGGKTAAGYGRLVRVDEFDSRRPRRPVRGSPELDAFRAWAAARRDDEEMPKRQILEDFEREWLPRLSRLAPDAREVCAAALRHLVPKHRKFGPWRDALIARMMEA
>NZ_CP022203.1|WP_095961271.1|8684475_8684868_-|type-III-B-CRISPR-module-associated-protein-Cmr5
MTGQTREQRRALEVYARVREVRDRHPRLCAEYKPRVNGLGAAVLRDGLAAALSFLERERTPATDRLLEDLAVCLAQVLSKPGLRGEELPEAVRNLKLEAYMLATREALRLLVWFRRAVQSTFPAEASSHG
>NZ_CP022203.1|WP_095961272.1|8684864_8685809_-|type-III-B-CRISPR-module-RAMP-protein-Cmr4
MECRPYLLHALSPLHVGTGQSVGVIDLPLARQKATGIPIVPGSSLKGVLRELRRPREESGSASGLHDAVFGPRRKKPGVEGDEPGDYAGALVVGDARLLALPVRSFVGTFALVTSPLLLALARRDLGALAEAWPVVAPLEGRRAQVASLKGSLVVYSAEGSAAAVYLEDLDLPVAQEPDTALATWAQGLAGLLPDAERELLTRRLVLVDDETMSFLWETATQVDTRVSIEPDTGTAADGHLWTEESLPAETLLVGVLGATGTFNAAPRKLTPDEVLGEALGGEGAVLQLGGKATVGRGRCRLSAWRPSVVGGAR
>NZ_CP022203.1|WP_095961273.1|8685811_8687023_-|CRISPR-associated-protein-Crm3
MNDARFALLPRDGLSAKDGRGWYTSEVGRGHSLPWPLPTTVRGALRAAWGHDVMAAEGITLSPDRWERDSERVALQRFIALRRGLGEPSFTRDHRMWPVPADAVRVLDANGEERVVSLQPRPGGAATLGPDEDAAREALWHPRREEGGKPLAPPLFWPEPRMMAWLRGAPDLLTPAPEAPSRRTDIHLAIDVATQAAQDSMLHSREVVEWLRAQRREAGRLLVEEWALGVACAWPELADGPPRGPVGLGGRRRLTDVERLDADLFAMPEGLAQTTRGLRLVLATPAEFRRGWLPDGLELESGTPPRYVGRLPGLAAPVVLRAALVPRPLDVSGWDMVRRRPRPTRRWVPAGAVYFFEKHCGEDFTADELRALWLASWGGGHAEALGQVLPGVWQPPLPHGQGA
>NZ_CP022203.1|WP_095961274.1|8687015_8688818_-|type-III-B-CRISPR-associated-protein-Cas10/Cmr2
MRYVIVLKVGPVQGFIAQARRTRDLWYGSQLLSLLAREMARDLTASGATLIFPHPDQVRDTSTGVANKVVALVDGVPEQVARRARDAAKSLLRSEWRRVAGRCESLLIQEAEALAEEQLEAFLEVHAAWAPVDASPTGYAKALREAEGALEARRGLREFSPWTRSPPEGTHKSSLDGGRPSLLRRDRERGPIWRELRIGLREELDALGLLKRAGGRPGQFVPVPSIGLAAGLHAASKAHADLLGRLKAQCEARNFQAVRAPSRPWVRDFPFDGQLLLPERWQPYFEECAIPDARRSAASFGRDFVEPLRAAMRSRGAEPIPYVACLVADGDHMGRALARLAEAPDGARAHQRVSQALAGFTQQARRIVEVEHRGVLVYAGGDDVLAFVTPADAPACAQDLATTFRATLAAALAGTDAVVPTLSVGLGVGHVLESLGALLDLGRRAEAAAKKAGRDALAILVAKHAGRERLWTAPWRMHPVERLSRDITLLTREPWPLPLGKVHEVADLERRFPPGSAPGPELAALLKDEAGRILARAEAGRAPAPLTPGDVGLELSSEGAASVSPHLALEQWSSRLLVADTFARAGRGLGFLQESEVRDE
>NZ_CP022203.1|WP_095961275.1|8688822_8690298_-|CRISPR-associated-protein-Cmr1
MRSLLDLPEPDSTDLAHLRRRSASAPRLETFTLALKTITPILGGGPVARSPELPSVDIIRVPTLRGHLRFWWRALYGHAYVARGTEGAWELARKERELWGGMGRAGGVDDAGPRRSQVELRVTEVQQAQGDSSDVDRAPRGVYALWPAITKPGLRDLPRWRPGLRFTLEVVAPEGEAMLQVRNAVRAWILFGGYGSRGRRGCGSVDVATGDKAIREQWLPAEASREALRQLMGGLPLFLARPEAPRCDMPLLQDAFLYRAHRRAPYSSGVAAWEVALQWLRDFRQGTESWGDGLPLPARNPKKEGREGRSNWPEADKIRRFARPSPKDEVGTATGRAYPEEHAPRPGHSASPAWPRAGFGLPIAFRFQRENKHKTPYSPQEPVGCVLQWARKNNGKWERMDRLASPLIVKAMPLSNGQFEPVALWLHRGTPVNGRVVVVQGKAVLSRSEVAFERSFRASDDQPLFSPLQRADNLRDAFFQWLKDTQKAQEA
>NZ_CP022203.1|WP_095961276.1|8690395_8692225_-|SAVED-domain-containing-protein
MRSEDIPITPRTRALIVRYEQDRPVIEATARDTLIRYGLEGDRDVASVVLHPHDPARAARSLPGQDWSEAFSEHERFAAALLKREAELHLDHLPVHIFGCAPLALMLELASRLPRRPVCVYQQAQDGSWSLGYDRMTAPSAEDFFQVEGLPSGRQGGRGHVLLVVEVTRAIRDNVRSKVSAWLPEASILTTVCLRPAAGPSPTAVQNPGQAARAAAQFREVLDKLHELLEGAESVVLAIDAPGSFAAALGTAVNPTTQHPLTLLHFNAERQLYDRVHVIRARRDVAPRVPTADDKLTAMRVLREVQKVHKELVSWLKEPEQQPFVEHIDGQAYLRSEIEDEPAYERTPLFRHGAGKWKLDWELLLGLGALLKRLQSQEDWKECLRLFLIHEAFHVRQGGLTSYNYRGIGRAGFVLEAADYDADAVGVEVALAWRKARQGGTVKDVGQVKTLESIVWNSLEILRVFEPERPVRELAERRLRRYLIWLFHACRFSALALRSPDAEVREELERVTVELVGLPAFRDPHESYFQQRVRLSLEDSREEVMLALYFRHRLVRMDNARAWVEDLLQALREWEAPPREELQDRVRLLFERLFDRHPELVSPRLPGAR
>NZ_CP022203.1|WP_170114795.1|8692326_8693247_-|nucleotidyltransferase
MDNEFPARRVMRSVGHALQEAIESLELPPEQHRRVTARMQEVQQRLRAVFGPKTDFLSGSYGRGTSIRPLNDIDFFIVLGDVLMTAAPARPLLPSDALRELRDGIHKEIPRRNMPAIQLHSVRVEFEETPIQFDVIPAYACSNGPGYLIPERKKDQSEEKWVRTDPRRHQEACATANKRCEGRLHSLIKLVKHWNRKQHSPLKSFHLEVMSYSVQLPRLSRESGHLESLETLFAHLARGVMNRCTDPAELGDDVDVYLSPSQRSAASQLLDGAAREVRLAREEQDTHPARAHARMKKLFPDLYQGY
>NZ_CP022203.1|WP_095961278.1|8693343_8694201_-|serine/threonine-protein-kinase
MLVRGTQVGAHVIVRRVAVGAFSDVYSGLHAVDGTQVAVKVLSASSCLHEELVARFLNEGQSLRDLRHPGLVRALDLGLLPDGPPFIVLEWLPTDLEQALARAGGCLPVRTCAEVLGQVAAALDALHVHGLIHRDVKPANILVARLDAEDVTVKLADLGLAKRVATGPEAPAALPVSTAGTAVLGSWDFMAPEQWLDAKRVDARVDVYSLGVLGFQLLAGQLPFGGGTQKELMIRHLRMPPPLHLLGDEVPASLRGLLGRMMAKAAGTRPPLMEVRECVAGLVFR
>NZ_CP022203.1|WP_095961279.1|8694200_8695025_-|sigma-70-family-RNA-polymerase-sigma-factor
MKKPPLLELSVEALIRLAKEGDSAALEELLTRFHDVIQAHAKRYGKPYGPGGTRPSDLSQLASMRVLQQFSTFKGQSEGELRGWLKRVVASQVVQTVRHATRQKRDESDAVPFDSDEARNAPTRQRSPSQVVSQQQEALQLIRSIHTELSGGQSDVVKAYYLDGHSLKDIALQMDKSEDAVASLMQRGVGALKQYFLGERVAGDGDEDAAKQSRLDNAFLAYLRRLAAETDVDPVSFAAGYSDCSPELERLLLWAGRLQALRPPEPFGTGGTED

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Crispr_ID: NZ_CP022203_19

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP022203_19

8817584-8817701

Orphan

Consensus_repeat	Method
CGCCTGACGTCGCTTCGGCGCACGAAGAAGGCGCTGGAG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP022203_19

>merge|NZ_CP022203|19|8817584-8817701|CRISPRCasFinder
CGCCTGACGTCGCTTCGGCGCACGAAGAAGGCGCTGGAGCCCAGCCGCATGCGGGCGCGGCGCAAGCTCCGTGCGCCCCCGCCTGACGTCGCTTCGGCGCACGAAGAAGGCGCTGGAG

>NZ_CP022203|19|13|8817584-8817701|CRISPRCasFinder
CGCCTGACGTCGCTTCGGCGCACGAAGAAGGCGCTGGAG	CCCAGCCGCATGCGGGCGCGGCGCAAGCTCCGTGCGCCCC
CGCCTGACGTCGCTTCGGCGCACGAAGAAGGCGCTGGAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP022203.1\|WP_095961349.1\|8827312_8828188_-\|tryptophan-2,3-dioxygenase	unknown	unknown	gnl\|CDD\|188272
NZ_CP022203.1\|WP_043709838.1\|8809206_8810079_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|373664
NZ_CP022203.1\|WP_013936962.1\|8815866_8816298_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961340.1\|8806591_8807701_+\|CBS-domain-containing-protein	unknown	unknown	gnl\|CDD\|341390
NZ_CP022203.1\|WP_013936957.1\|8820021_8820432_-\|type-II-secretion-system-protein-GspG	unknown	unknown	gnl\|CDD\|130771
NZ_CP022203.1\|WP_013936972.1\|8808588_8809167_-\|YceI-family-protein	unknown	unknown	gnl\|CDD\|377274
NZ_CP022203.1\|WP_095961347.1\|8818483_8819845_-\|universal-stress-protein	unknown	unknown	gnl\|CDD\|366180
NZ_CP022203.1\|WP_095961344.1\|8813694_8814819_-\|LysM-peptidoglycan-binding-domain-containing-protein	unknown	unknown	gnl\|CDD\|225720
NZ_CP022203.1\|WP_013936953.1\|8826049_8827171_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961350.1\|8829055_8829613_-\|hemerythrin-domain-containing-protein	unknown	unknown	gnl\|CDD\|376622
NZ_CP022203.1\|WP_095961341.1\|8807773_8808592_-\|Rieske-2Fe-2S-domain-containing-protein	unknown	unknown	gnl\|CDD\|239550
NZ_CP022203.1\|WP_095961806.1\|8821994_8823047_-\|thrombospondin-type-3-repeat-containing-protein	unknown	unknown	gnl\|CDD\|143586
NZ_CP022203.1\|WP_095961343.1\|8811879_8813238_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961805.1\|8810478_8811072_-\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|378915
NZ_CP022203.1\|WP_095961346.1\|8817750_8818347_-\|Fis-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225114
NZ_CP022203.1\|WP_095961345.1\|8816447_8816915_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_043709822.1\|8828317_8828854_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961342.1\|8811057_8811849_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP022203.1\|WP_095961348.1\|8823043_8825956_-\|GAF-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP022203.1\|WP_043709825.1\|8820486_8821947_-\|response-regulator	unknown	unknown	gnl\|CDD\|143636

Protein	Function_ID	Function_description	E-value
NZ_CP022203.1\|WP_043709838.1\|8809206_8810079_-\|hypothetical-protein	gnl\|CDD\|373664	pfam15231, VCX_VCY, Variable charge X/Y family. The variable charge X/Y (VCX/VCY) family of proteins has members on the Human X and Y chromosomes, is expressed in male germ calls and may play a role in spermatogenesis or in sex ratio distortion.	0.000367983
NZ_CP022203.1\|WP_095961806.1\|8821994_8823047_-\|thrombospondin-type-3-repeat-containing-protein	gnl\|CDD\|143586	cd07185, OmpA_C-like, Peptidoglycan binding domains similar to the C-terminal domain of outer-membrane protein OmpA. OmpA-like domains (named after the C-terminal domain of Escherichia coli OmpA protein) have been shown to non-covalently associate with peptidoglycan, a network of glycan chains composed of disaccharides, which are crosslinked via short peptide bridges. Well-studied members of this family include the Escherichia coli outer membrane protein OmpA, the Escherichia coli lipoprotein PAL, Neisseria meningitdis RmpM, which interact with the outer membrane, as well as the Escherichia coli motor protein MotB, and the Vibrio flagellar motor proteins PomB and MotY, which interact with the inner membrane.	1.31911e-33
NZ_CP022203.1\|WP_095961340.1\|8806591_8807701_+\|CBS-domain-containing-protein	gnl\|CDD\|341390	cd04622, CBS_pair_HRP1_like, CBS pair domain found in Hypoxic Response Protein 1 (HRP1) -like proteinds. Mycobacterium tuberculosis adapts to cellular stresses by upregulation of the dormancy survival regulon. Hypoxic response protein 1 (HRP1) is encoded by one of the most strongly upregulated genes in the dormancy survival regulon. HRP1 is a 'CBS-domain-only protein; however unlike other CBS containing proteins it does not appear to bind AMP. The biological function of the protein remains unclear, but is thought to contribute to the modulation of the host immune response. The CBS domain, named after human CBS, is a small domain originally identified in cystathionine beta-synthase and is subsequently found in a wide range of different proteins. CBS domains usually occur in tandem repeats. They associate to form a so-called Bateman domain or a CBS pair based on crystallographic studies in bacteria. The CBS pair was used as a basis for this cd hierarchy since the human CBS proteins can adopt the typical core structure and form an intramolecular CBS pair. The interface between the two CBS domains forms a cleft that is a potential ligand binding site. The CBS pair coexists with a variety of other functional domains and this has been used to help in its classification here. It has been proposed that the CBS domain may play a regulatory role, although its exact function is unknown. Mutations of conserved residues within this domain are associated with a variety of human hereditary diseases, including congenital myotonia, idiopathic generalized epilepsy, hypercalciuric nephrolithiasis, and classic Bartter syndrome (CLC chloride channel family members), Wolff-Parkinson-White syndrome (gamma 2 subunit of AMP-activated protein kinase), retinitis pigmentosa (IMP dehydrogenase-1), and homocystinuria (cystathionine beta-synthase).	7.20724e-49
NZ_CP022203.1\|WP_013936957.1\|8820021_8820432_-\|type-II-secretion-system-protein-GspG	gnl\|CDD\|130771	TIGR01710, Type_II_secretion_system_protein_G, type II secretion system protein G. This model represents GspG, protein G of the main terminal branch of the general secretion pathway, also called type II secretion. It transports folded proteins across the bacterial outer membrane and is widely distributed in Gram-negative pathogens. [Protein fate, Protein and peptide secretion and trafficking, Cellular processes, Pathogenesis].	5.21905e-11
NZ_CP022203.1\|WP_013936972.1\|8808588_8809167_-\|YceI-family-protein	gnl\|CDD\|377274	pfam04264, YceI, YceI-like domain. E. coli YceI is a base-induced periplasmic protein. The recent structure of a member of this family shows that it binds to poly-isoprenoid. The structure consists of an extended, eight-stranded, antiparallel beta-barrel that resembles the lipocalin fold.	1.92686e-18
NZ_CP022203.1\|WP_095961347.1\|8818483_8819845_-\|universal-stress-protein	gnl\|CDD\|366180	pfam00582, Usp, Universal stress protein family. The universal stress protein UspA is a small cytoplasmic bacterial protein whose expression is enhanced when the cell is exposed to stress agents. UspA enhances the rate of cell survival during prolonged exposure to such conditions, and may provide a general "stress endurance" activity. The crystal structure of Haemophilus influenzae UspA reveals an alpha/beta fold similar to that of the Methanococcus jannaschii MJ0577 protein, which binds ATP, though UspA lacks ATP-binding activity.	8.96288e-13
NZ_CP022203.1\|WP_095961344.1\|8813694_8814819_-\|LysM-peptidoglycan-binding-domain-containing-protein	gnl\|CDD\|225720	COG3179, COG3179, Predicted chitinase [General function prediction only].	2.05082e-39
NZ_CP022203.1\|WP_095961349.1\|8827312_8828188_-\|tryptophan-2,3-dioxygenase	gnl\|CDD\|188272	TIGR03036, trp_2_3_diox, tryptophan 2,3-dioxygenase. Members of this family are tryptophan 2,3-dioxygenase, as confirmed by several experimental characterizations, and by conserved operon structure for many of the other members. This enzyme represents the first of a two-step degradation to L-kynurenine, and a three-step pathway (via kynurenine) to anthranilate plus alanine. [Energy metabolism, Amino acids and amines].	4.09411e-143
NZ_CP022203.1\|WP_095961350.1\|8829055_8829613_-\|hemerythrin-domain-containing-protein	gnl\|CDD\|376622	pfam01814, Hemerythrin, Hemerythrin HHE cation binding domain. Iteration of the HHE family found it to be related to Hemerythrin. It also demonstrated that what has been described as a single domain in fact consists of two cation binding domains. Members of this family occur all across nature and are involved in a variety of processes. For instance, in Nereis diversicolor hemerythrin binds Cadmium so as to protect the organism from toxicity. However Hemerythrin is classically described as Oxygen-binding through two attached Fe2+ ions. And the bacterial NorA is a regulator of response to NO, which suggests yet another set-up for its metal ligands. In Staphylococcus aureus the iron-sulfur cluster repair protein ScdA has been noted to be important when the organism switches to living in environments with low oxygen concentrations; perhaps this protein acts as an oxygen store or scavenger.	2.01715e-08
NZ_CP022203.1\|WP_095961341.1\|8807773_8808592_-\|Rieske-2Fe-2S-domain-containing-protein	gnl\|CDD\|239550	cd03467, Rieske, Rieske domain; a [2Fe-2S] cluster binding domain commonly found in Rieske non-heme iron oxygenase (RO) systems such as naphthalene and biphenyl dioxygenases, as well as in plant/cyanobacterial chloroplast b6f and mitochondrial cytochrome bc(1) complexes. The Rieske domain can be divided into two subdomains, with an incomplete six-stranded, antiparallel beta-barrel at one end, and an iron-sulfur cluster binding subdomain at the other. The Rieske iron-sulfur center contains a [2Fe-2S] cluster, which is involved in electron transfer, and is liganded to two histidine and two cysteine residues present in conserved sequences called Rieske motifs. In RO systems, the N-terminal Rieske domain of the alpha subunit acts as an electron shuttle that accepts electrons from a reductase or ferredoxin component and transfers them to the mononuclear iron in the alpha subunit C-terminal domain to be used for catalysis.	3.31561e-14
NZ_CP022203.1\|WP_095961805.1\|8810478_8811072_-\|nuclear-transport-factor-2-family-protein	gnl\|CDD\|378915	pfam12680, SnoaL_2, SnoaL-like domain. This family contains a large number of proteins that share the SnoaL fold.	2.76539e-15
NZ_CP022203.1\|WP_095961346.1\|8817750_8818347_-\|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].	0.00147419
NZ_CP022203.1\|WP_095961348.1\|8823043_8825956_-\|GAF-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.95068e-51
NZ_CP022203.1\|WP_043709825.1\|8820486_8821947_-\|response-regulator	gnl\|CDD\|143636	cd07302, CHD, cyclase homology domain. Catalytic domains of the mononucleotidyl cyclases (MNC's), also called cyclase homology domains (CHDs), are part of the class III nucleotidyl cyclases. This class includes eukaryotic and prokaryotic adenylate cyclases (AC's) and guanylate cyclases (GC's). They seem to share a common catalytic mechanism in their requirement for two magnesium ions to bind the polyphosphate moiety of the nucleotide.	1.12449e-66

>NZ_CP022203.1|WP_095961345.1|8816447_8816915_-|hypothetical-protein
MSQDNAGKPKRGLKRPIEVVRAELLKDPETKKIAEAVSMKLEDYVELVLKYAQDKDKEAEVAVISDEELRRNGFNPLSAEEAANILIKGMKGELPGSPPDFEASKFTQDKASTAGKPSLTAPPPAGATPIGPQDPAARQELMDQLKKGGSGGNRP
>NZ_CP022203.1|WP_013936962.1|8815866_8816298_-|hypothetical-protein
MGSALKGITKAISNVASTVSKIAGGIANIGGKAMEFLQKPLSSLVSPIASFIGDKVGKLPFVGKFLGPIAENLVKQGASSFLGEGTLGSLGFMSKIAPKVQDITNIAQTVKGAADKVGAFVDNPLGQQNFQNIIAQNHARFVE
>NZ_CP022203.1|WP_095961344.1|8813694_8814819_-|LysM-peptidoglycan-binding-domain-containing-protein
MTTYSVRRGDTLSALAQRFKTSVSSLAKTNGISNPNLIYAGQQLRIPDGFDAPRASGGGRAASSYTVKSGDTLSGIAGRHGTSVGALAKANNISNPDRIYVGQKLTIPGSGGAAPTRPSTGGGGGGSYTVKSGDTLSGIAGRHGTTVGALAKANNISNPNLIYVGQRLTIPGGGGASPTRPTPNQPPVGGVGGPKPPTGGSAGVTVQQLRAVMPNLSQAKAEQYLPHLNRAMAEANITTPKRKAAFLAQLAHESGQLRYMEEIASGAAYEGRRDLGNTQPGDGVRYKGRGPIQLTGRANYRAAGRALGIDLEGNPQRAKDPDVAFRIAGWYWSSRNLNTYADAGNFREVTRRINGGYNGMADREMYYRRALNVF
>NZ_CP022203.1|WP_095961343.1|8811879_8813238_-|hypothetical-protein
MSPHRNELRAFDGSAAKTPEPTPRGGSTPASAGPARSAGELAVLGGWSRPGATKEPPTDVLEDLRARLTRSLENWTVGADDVRAVHTALGGLPSGTYRATLERMQHDGLLSAYVKAQDAGARLAFLEQAESKGVLQRRNGEAGPVGALGYPAVPDVFVNDRRLPEAMRDAVNAHATDVGAGFYRAHTEYLGRYARAVDGAQSLQELGALGPPRAAHLPESILGLEWKDPARRDYETAWKVGIGQPKSLNLTLQHVSARQRELSGERAGGTVRLHGKVGVSNEHVQWGAKAALDTRGHGDLKGEVGVAARNGPVGIEVSHDSAGDTDVKLKLKLGLAELSLDSDGEQRVAVGVGTLFQVHAALNPKKAELGGGVSAKFKADDGSQASVEAGFSMKGLTAERAGQAVDREHRGVFQPPAELASRTAWDALPEATRATYAKEGWNREAWTRALPR
>NZ_CP022203.1|WP_095961342.1|8811057_8811849_+|hypothetical-protein
MTSTHTRPTPSMSDSPVESLAPLPAAASLTALREALGSPGVIPAEVDALLAAMAQAPEGDEARRARTDFLLSLMTLPGDASVQTGSAGITVRTAAVEALLELGYPYALEVPPDALAWARRERGTSRRGAPASRLSPPKLAVAVTALCAVLQLFFVFSTYRSALGNGMLWEELLLVLAAVTPALLATLGVWLRARPLQSLGSVGLGLQGLFWLGALLLFAWLTEHSDWLWLALPWYLPLISAYLMWPRREPDEPGAVLPEPAPP
>NZ_CP022203.1|WP_095961805.1|8810478_8811072_-|nuclear-transport-factor-2-family-protein
MRGGHGRKAVTLPPGPVASPPPGRPEGEGPGLPGGHAPEACAPFPCVTLSRGARQRMAMERAQRFVEALTKLEKEGDLEAIVSLFSDDAQVSNVASPQVFSGQEGARRFWREYKGTLQRVESTFRNMIEAGSRVALEWETQGTAHNGAAVAYEGVSIIEWDGDRIRRFYAYFDPHALGLELTQGNAPRTEVPATTPA
>NZ_CP022203.1|WP_043709838.1|8809206_8810079_-|hypothetical-protein
MTRFAALFVVLSLIAAPHTAWAQRSQTESAKKTRAVKSSSKAAKTKATKGKTTRASSKAKAGKKATRRKKAAPAVDSKQVGAPAVQPARPTMQVEPARPLAPTEDAPTVQKSDEAPAEGGDSLDFDLLEPAEAATAAQVDPDLEKRIGRRRTMLKLHQGLGFAMAAGLVGTTVVGQLQFNDSFRGGGDDRNLLGLHRGLAIGTSALFASVGLLGLLAPEPFEKEFQWDTITVHKMFMALATVGMVAQIVLGIMATDRFGRLSETDLATAHQISGYVTLGAVSAGVFTLFF
>NZ_CP022203.1|WP_013936972.1|8808588_8809167_-|YceI-family-protein
MIARRIALIATLVLALPAVAQSQARTYNVKKDASSLTYKLKHKLHEVVGKAPPSDGKARLLPDGTLQVAVRANVKDFDSGNANRDAHMMETTDAAKFPIIDFKGVATGVKTPKSFPAKVPVKVKGQLTFHGVKKTVEIPMTVEFKSEKEAVAEGTFDISLDAYNVERPSLMMVKVDDLLVLEPKLVFEVEGT
>NZ_CP022203.1|WP_095961341.1|8807773_8808592_-|Rieske-2Fe-2S-domain-containing-protein
MSSTRRGFLKGILGTGAASAAATTLPGCAPDINPAPVTDVTASDAGTVDILVSRYPDLEPVGGALTVRVPGEQVPLLVVHSKDDGAPDDFSVLSSLCTHVGCPLGFDGKDVICPCHLSRFSATDGSVLQRPATVPLQTFAAEYNPNTGVVRINLRAGQSDFPPAVDGQVVLPFSDFPQLRGLGGSVTGVPSGYGKRIFVFRLQDGSLSAVDSVCTHAFCEVNYREQEADLFCACHASIFTKDGAVTQGPATIPLKKFTVSETGDSVVLTGVA
>NZ_CP022203.1|WP_095961340.1|8806591_8807701_+|CBS-domain-containing-protein
MAHRSTDNGRDETHGARRTLPSEPTAHREADVAPPGSRERAESDLTGWNPARDEAASTRQGRYHRAATMRMAQPRTQVDDGPRQDGYGAPPEGSGPYGLDDRDSHYATGWGPRHDTGEQDVELSRQRADYRPWDRSGYGGDEPPRTVAPQAESRDARARASHGEERHGDARPRYRMERSPSDAASLHAHRSAGPGRDEASTPYRRDTRAEDRGRRGRWQHEPLTAREVMTRNVRTARPESPLREVAQIMKDESCGAVPIVDERGRLVGIVTDRDLVVRAFTGGRSPDQLRVSDVMTDDVEAVTQDDTLHDVIGLMGRRQLRRIPVVERDDCIVGIISLGDIALRADHDEALQQALERISSKRSFWSRLG
>NZ_CP022203.1|WP_095961346.1|8817750_8818347_-|Fis-family-transcriptional-regulator
MTSKGYREVELVCNRSSLLLHGGTEEERRSWAQEAARNFDVELVEVRQAAELPQALRQPDGVVFIADVAKLGRDAQFALLRCLQTQEERPKLVLGVSGSADAALARGTLRDDLHYRLHQAQVDLQKDGLRELLKHRWAQQAEQLAQKAAAARTAEEAARQAAIARLPGTVTRIAPRQKAKPVGGNASRAKGVPRNAAR
>NZ_CP022203.1|WP_095961347.1|8818483_8819845_-|universal-stress-protein
MAIVCVTNLSPESLAAAHVAAAVAGRLQEPLLLLGISEGDAFLDEGTGALTLTQQRLEAEAARLETLARVVRYRLQAGTSADEVLSDEECRRARWIVVAASGWRGSAWRRATVPERLSRYGCAPVLAVRSDTALTDWARGRRRLLVLVGVDPGSSTTGAAVSFLRELRRVGPCDVLATYVCSPMDERERLGIHSPVHVELLEPGLQGMEALDPLVERVLQREVREQVGELLGEGRVEVVLEPGFGRPADHLMHVAHTRGADLMVVGTHQRSGVKRLWHGSVSAGVLRHAAQSVVCVPPMVQGRRADRAPRSVLVPVDFSEASAKAISQARTLVGPGGRVHLLHVHRRKLEDRGFMDHYGVLPEPARDRDGVLQRLWELVPRDEGAQTVRWSVEGVTGEDVTLAICQATEREGVDLVCVGTSLEPSRLRDALEGEVAHELVARCRRPVMVVPSA
>NZ_CP022203.1|WP_013936957.1|8820021_8820432_-|type-II-secretion-system-protein-GspG
MNASDEPPPSRRSPVLFVGLVFGLGLVVAILVGALSGSKAIHADRIHQDFVVLEEALGRYRADKGALPEEADLEALLVPAYLPSVPLDPWGRAYRYTSNGEQVFLATFGKSDDRGGAGEEQDHTNHDGHAAPKVAR
>NZ_CP022203.1|WP_043709825.1|8820486_8821947_-|response-regulator
MSASSPLFGDLLLKLGIVSPSQVQEALALQALTGQRVGEALISLGYVTREQIQDALGEALGLHQDKSPLQPALGELLVGLKYVTLAQLDEGLARQRRDGRKLGEILVELGHCTYKQIYEALGLQNRIAGRQDLARPTSDGRRRVVVVDDSPLACAFVQEGLVALGYEVLCFQDPFEALESMGRLQPVIVLSDLEMPGLDGVELCRRLKEGPRHAVPVIILTANDVEAERVRGLRAGADDYVNKSASMDELAARIESVVRRTGETERMRKLFARYTSDAVVEEILKSADAVVLTGEKREVTLLFADIRNFTGLAESLPPEQVVGVLNQVLGRMSDAVLTCGGTLDKFLGDGLMAVFGAPVARPDDALRALQCAKMMMDALTDLRIEAEAEWAANGREGQPLALELGIGINSGVVVAGNIGSTVRAEYTCIGDAVNVAARLCALAGPGEILVGERTRELVDANETAFEDLPPVRLKGKQQPVPLFRAL
>NZ_CP022203.1|WP_095961806.1|8821994_8823047_-|thrombospondin-type-3-repeat-containing-protein
MSVWTGRTRCALVPRMTTRALHRWVLLAAVLGAFAPGCRHAPDLNPALDADGDGVLNGEDACPTARGLARLQGCPAKDTDGDGVEDALDTCPRRAGPASRDGCPIRDSDEDGVEDAKDACPRVFGPLERQGCPVEDPDRDGVEGAADKCPDEPGPASREGCPIRDADGDGVPDEEDACPTEEGLPALRGCPERDMDGDSVPDHRDNCPRERGAADNQGCPAARKQRVGIRPDRLELLERITFVPGTATLHPRVQPVLDNVAEVLLAHPRLGVIAVEGHTDNRGDPEVQREMTRARAEVVRDYLVERGVPADRLEAWGFGPDRPVGSNETSQGRAANRRLDLRIVTPRGRP
>NZ_CP022203.1|WP_095961348.1|8823043_8825956_-|GAF-domain-containing-protein
MHPCRGEWGMKVPGKTMGAAVDRMSRALERLSAAPPVVAVLEELLCQASSALGASGAFLCWWGGTGDLSTLTTQGVDAEAAAVCAQRLLAQAPGPGEPRLPRVVEDVSRDALLASEPDARRELGAGALLSQPLFFAGGLGAAGVLGVLFREAWRPAEGDLQRFGLSVKLAALALERERMAETLRQSVLSARAEVEETEVLRLRRFQAVTEAFGRALSWDEVARVVLEQGLPAVGASLGMVHLVVPDGTVALKAAVGLSDAQKQALHVPPWRGGGTSGADAGGLSSPLWLETPAAVRDALPGLVSLLAPEPPRALVLLPLHVEGRTFGTLCFGFSEARRFSALERASITGLGHECGQALERARLYARERTARLQAEAAGQRLRLLADASALVSASLDWEETVAGVARLALGHFADGCAVDSYEDGVVRRLAVLYENPHTAPRGLELLRFTPQEGSPTLLAEVLASGRPWMMARPTSEPGDTRTAAARLYAAARELGVGSLILTPLVARQRTLGVLTFMRGAGSVPFDIPDLSLAEELAGRAALAIDNADLFRKARAAEEESRRGAARLHVLVQVSHLIAEAGLDLPTVLEVLVRKVSEALGDACVLQLLSEDKAHLDLVSVHHPDAEARAVLDASMRRCPARVGEGLSGRVAATGQPLFVPRLQAEDLRDERVPQGMPFLQRYGPHSVIVVPLGVRGRVLGTLGVMREARGREYSVEERALLESLAARAALAIEDARRYGAATQAVKARDEMLSVAGHELKSPLNALQLQIHLLARMAREAMAVDGLAERAERAAKAGQRLGLLIDDLLDVSRLSSGRLGLKREEVDLAALTRELVGRMSEELALAGSEVRLVLDEPVSGQWDRLRLEQVLVNLLSNAAKYGAGRPVTVEVGAVGPVARLSVRDEGIGVSPDEQERIFEQFERSASVQHFKGLGLGLWITKRIIEAHGGSIRLTSEPGKGSTFTVELPLPA
>NZ_CP022203.1|WP_013936953.1|8826049_8827171_-|hypothetical-protein
MDAAAPLLFDKAYVLCYRTFDIAEELDLERARRVLTEDSRRLKLSRENSQYLQLPNPPLAYELGRRPLALRDGPVAVDATARLFDHGAASIILRVPVVPGTSLETLTRMADELYDSQALEDLALELVEGVRRTIAPAAQAPHLWEQNESYTVIFAEEIRGHPTAEELLKQADLAPLLLGESGTVPLSPRESESVLQSRFSYTIHDLVVIDWNSAFVYEPSGSRDIPDLLEIANAQLLEFRYYDERLDAHITRIHEKVQSARHGWATLFRSPYRSLARQTLSTLVDLNEFIERVENSLKIIGDFYLAKVYENAVRRMRIPPWQASVTRKQQLLAQTYGLLKGDVDIDRSHTLEAVIVLLIVLEIFFAVFRVFEH
>NZ_CP022203.1|WP_095961349.1|8827312_8828188_-|tryptophan-2,3-dioxygenase
MPGPMNKRDLEPGIITDLAGRTTYGDYLQLDRLLSAQVTRSQPPHHDELLFIIQHQTSELWMKLLIHELGACIRYVQADRLEPSFKIFARVAHIQRMLFEQWSVLETLTPNEYLEFRDTLGSSSGFQSFQYRALEFLLGNKDAQALTPFRHVPTIHGELERLFESPSLYDEFLRHLSRMGHPVPQSHAQRDWRKPYEKSPEVVEVFRRIYEDTEAHWDAYEMCEKLVDTEERFQLWRYRHMMTVMRIIGFKQGTGGSSGVGFLRKALDLRFFPELWDVRTELAPPPPRHRP
>NZ_CP022203.1|WP_043709822.1|8828317_8828854_-|hypothetical-protein
MSVDKAFRDMIRNEIEVQLKPLRDVVARLEEGTADLDALRNVAERLAPLAEVVGPLFGAQIPAAAKAGRRGPGRPAAARSSVTAAPAAAGGKRRGRKPAAAGADGARACAIIGCGKPSRTKGYCAAHYQKLRMLEKTNRRPSDWKDYADPDSVDDIKLPRGRAASKALAAAAQAGHAG
>NZ_CP022203.1|WP_095961350.1|8829055_8829613_-|hemerythrin-domain-containing-protein
MPARRHTQVVCFLVRAERSRMGSPFDILIDQHRELEERLERLVSGVEPEELRGLTAELLALLRLHSRLEERCLYPLMARVEGREVSRVQAEDHLTMRELMAELEELPAGHPEWQARLLTLEDLAVAHFQEEENARLPQLMIALDSLSLEDLRRDLSATREELLSRPQVFQVPGGAPLLESLSWDG

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP022203_9	9.2\|5086336\|22\|NZ_CP022203\|CRT	5086336-5086357	22	NZ_CP022203.1	5086246-5086267	0	1.0
NZ_CP022203_11	11.2\|5516673\|18\|NZ_CP022203\|CRT	5516673-5516690	18	NZ_CP022203.1	7158915-7158932	1	0.944
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	120621-120639	1	0.947
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	2621333-2621351	1	0.947
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	2818058-2818076	1	0.947
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	7853705-7853723	1	0.947
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NZ_CP022203.1	5212376-5212402	1	0.963
NZ_CP022203_8	8.1\|4795839\|20\|NZ_CP022203\|CRT	4795839-4795858	20	NZ_CP022203.1	6407828-6407847	2	0.9
NZ_CP022203_8	8.1\|4795839\|20\|NZ_CP022203\|CRT	4795839-4795858	20	NZ_CP022203.1	7999389-7999408	2	0.9
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	534003-534021	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	610179-610197	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	1613041-1613059	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	2714190-2714208	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	3565980-3565998	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	5314029-5314047	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	5709391-5709409	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	6187610-6187628	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	6759640-6759658	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	7135195-7135213	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	7341688-7341706	2	0.895
NZ_CP022203_11	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	NZ_CP022203.1	8684905-8684923	2	0.895

1. spacer 9.2|5086336|22|NZ_CP022203|CRT matches to position: 5086246-5086267, mismatch: 0, identity: 1.0

cgcggcaccggcctcaccggca	CRISPR spacer
cgcggcaccggcctcaccggca	Protospacer
**********************

2. spacer 11.2|5516673|18|NZ_CP022203|CRT matches to position: 7158915-7158932, mismatch: 1, identity: 0.944

ggacgcgccatggcgccc	CRISPR spacer
ggacgcgccgtggcgccc	Protospacer
*********.********

3. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 120621-120639, mismatch: 1, identity: 0.947

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgggcgcgggct	Protospacer
************** ****

4. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 2621333-2621351, mismatch: 1, identity: 0.947

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgggcgcccgct	Protospacer
*************** ***

5. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 2818058-2818076, mismatch: 1, identity: 0.947

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgggcggcggct	Protospacer
************* *****

6. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 7853705-7853723, mismatch: 1, identity: 0.947

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggagggcgccggct	Protospacer
******* ***********

7. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to position: 5212376-5212402, mismatch: 1, identity: 0.963

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
gtcgttcgggtccgtgcccagcgcaat	Protospacer
**.************************

8. spacer 8.1|4795839|20|NZ_CP022203|CRT matches to position: 6407828-6407847, mismatch: 2, identity: 0.9

cccgtgccggcgtcctcggt	CRISPR spacer
cccgtgccgccgtccttggt	Protospacer
********* ******.***

9. spacer 8.1|4795839|20|NZ_CP022203|CRT matches to position: 7999389-7999408, mismatch: 2, identity: 0.9

cccgtgccggcgtcctcggt	CRISPR spacer
cccgtgcggccgtcctcggt	Protospacer
******* * **********

10. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 534003-534021, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggctggcgcctgct	Protospacer
******** ****** ***

11. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 610179-610197, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgcgcgccgcct	Protospacer
********* ****** **

12. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 1613041-1613059, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgggcggcgcct	Protospacer
************* ** **

13. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 2714190-2714208, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgggagcaggct	Protospacer
*********** ** ****

14. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 3565980-3565998, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgggcggcgcct	Protospacer
************* ** **

15. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 5314029-5314047, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcccggcgggccccggct	Protospacer
*** ******** ******

16. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 5709391-5709409, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgccgcgggggccggct	Protospacer
***** ***** *******

17. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 6187610-6187628, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggccggcgcgggct	Protospacer
******** ***** ****

18. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 6759640-6759658, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgccgcgggcgcgggct	Protospacer
***** ******** ****

19. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 7135195-7135213, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcgcagggcgccggct	Protospacer
******  ***********

20. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 7341688-7341706, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggcgggcgcggcct	Protospacer
************** * **

21. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to position: 8684905-8684923, mismatch: 2, identity: 0.895

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggccggtgccggct	Protospacer
******** **.*******

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP022203_8	8.4\|4795962\|23\|NZ_CP022203\|CRT	4795962-4795984	23	NZ_CP054613	Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence	2340130-2340152	2	0.913
NZ_CP022203_9	9.2\|5086336\|22\|NZ_CP022203\|CRT	5086336-5086357	22	LN997845	Streptomyces reticuli genome assembly TUE45, plasmid : IV	3631-3652	2	0.909
NZ_CP022203_9	9.2\|5086336\|22\|NZ_CP022203\|CRT	5086336-5086357	22	LR743530	Xanthomonas phage Suba genome assembly, chromosome: 1	42965-42986	2	0.909
NZ_CP022203_9	9.2\|5086336\|22\|NZ_CP022203\|CRT	5086336-5086357	22	MN586047	Gordonia phage EMoore, complete genome	17712-17733	2	0.909
NZ_CP022203_9	9.3\|5086381\|22\|NZ_CP022203\|CRT	5086381-5086402	22	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	873443-873464	2	0.909
NZ_CP022203_4	4.1\|2964279\|25\|NZ_CP022203\|CRISPRCasFinder	2964279-2964303	25	MT536174	Stenotrophomonas phage vB_SmaS-AXL_3, complete genome	3125-3149	3	0.88
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP027299	Streptomyces sp. SGAir0924 plasmid unnamed_5	374927-374953	3	0.889
NZ_CP022203_4	4.1\|2964279\|25\|NZ_CP022203\|CRISPRCasFinder	2964279-2964303	25	NZ_CP029834	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence	370256-370280	4	0.84
NZ_CP022203_4	4.1\|2964279\|25\|NZ_CP022203\|CRISPRCasFinder	2964279-2964303	25	NZ_CP054617	Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence	239943-239967	4	0.84
NZ_CP022203_8	8.2\|4795878\|26\|NZ_CP022203\|CRT	4795878-4795903	26	NZ_CP020331	Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence	551593-551618	4	0.846
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP029358	Azospirillum sp. CFH 70021 plasmid unnamed3	381649-381675	4	0.852
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP032348	Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence	334163-334189	4	0.852
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	230041-230067	4	0.852
NZ_CP022203_4	4.1\|2964279\|25\|NZ_CP022203\|CRISPRCasFinder	2964279-2964303	25	NZ_CP034431	Bradyrhizobium sp. LCT2 plasmid pLCT2, complete sequence	124534-124558	5	0.8
NZ_CP022203_8	8.2\|4795878\|26\|NZ_CP022203\|CRT	4795878-4795903	26	NZ_CP054613	Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence	2340130-2340155	5	0.808
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	1253773-1253802	5	0.833
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP012944	Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence	1274409-1274438	5	0.833
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP012940	Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence	620033-620062	5	0.833
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NC_017575	Ralstonia solanacearum Po82 megaplasmid, complete sequence	1123417-1123446	5	0.833
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP026308	Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence	1123363-1123392	5	0.833
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP051295	Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence	612005-612034	5	0.833
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NZ_CP029830	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence	862572-862601	5	0.833
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NC_011961	Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence	246589-246615	5	0.815
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1072628-1072654	5	0.815
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	572702-572728	5	0.815
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP032054	Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence	674358-674384	5	0.815
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP016560	Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence	331614-331640	5	0.815
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	609392-609418	5	0.815
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_CP022417	Sulfitobacter pseudonitzschiae strain SMR1 plasmid pSMR1-2, complete sequence	237194-237220	5	0.815
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NZ_CP035514	Haematobacter massiliensis strain OT1 plasmid pOT1-4, complete sequence	77196-77222	5	0.815
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NZ_CP025810	Sulfitobacter sp. SK025 plasmid unnamed2, complete sequence	173683-173709	5	0.815
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NZ_CP044976	Hydrogenophaga sp. PBL-H3 substr. PBL-H3(B2) plasmid pPBL-H3_B2-1, complete sequence	46253-46279	5	0.815
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	47913-47943	6	0.806
NZ_CP022203_8	8.2\|4795878\|26\|NZ_CP022203\|CRT	4795878-4795903	26	MN204493	Streptomyces phage Zuko, complete genome	16166-16191	6	0.769
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP021367	Acidovorax carolinensis strain P4 plasmid pACP4.1, complete sequence	12482-12511	6	0.8
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP021363	Acidovorax carolinensis strain P3 plasmid pACP3.1, complete sequence	256617-256646	6	0.8
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	753744-753770	6	0.778
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NC_017966	Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence	614198-614224	6	0.778
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NC_025024	Burkholderia glumae strain BGR1 plasmid pBGA40, complete sequence	2912-2938	6	0.778
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	1527754-1527780	6	0.778
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	313309-313335	6	0.778
NZ_CP022203_16	16.30\|8645321\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8645321-8645354	34	NZ_CP007130	Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence	803382-803415	6	0.824
NZ_CP022203_16	16.45\|8646397\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646397-8646431	35	NZ_CP013109	Sinorhizobium americanum strain CFNEI 73 plasmid B, complete sequence	285955-285989	6	0.829
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1781389-1781419	7	0.774
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	31873-31903	7	0.774
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NZ_CP038638	Cupriavidus oxalaticus strain X32 plasmid unnamed3, complete sequence	32223-32253	7	0.774
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_AP022319	Burkholderia sp. THE68 plasmid BTHE68_p1, complete sequence	65408-65441	7	0.794
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP013855	Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence	114240-114269	7	0.767
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP007794	Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence	485253-485282	7	0.767
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP054615	Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence	219311-219340	7	0.767
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP032322	Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence	647768-647797	7	0.767
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	KY092482	Streptomyces phage Mojorita, complete genome	23483-23512	7	0.767
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	KY092480	Streptomyces phage Picard, complete genome	23681-23710	7	0.767
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	1507903-1507929	7	0.741
NZ_CP022203_12	12.1\|6778349\|30\|NZ_CP022203\|PILER-CR	6778349-6778378	30	NC_019789	Deinococcus peraridilitoris DSM 19664 plasmid pDEIPE01, complete sequence	469456-469485	7	0.767
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NZ_CP045122	Rubrobacter sp. SCSIO 52915 plasmid unnamed1, complete sequence	32638-32664	7	0.741
NZ_CP022203_12	12.2\|6778418\|27\|NZ_CP022203\|PILER-CR	6778418-6778444	27	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	3412925-3412951	7	0.741
NZ_CP022203_17	17.1\|8648986\|32\|NZ_CP022203\|PILER-CR,CRISPRCasFinder,CRT	8648986-8649017	32	NZ_CP010630	Phaeobacter inhibens strain P78 plasmid pP78_a, complete sequence	49868-49899	7	0.781
NZ_CP022203_17	17.1\|8648986\|32\|NZ_CP022203\|PILER-CR,CRISPRCasFinder,CRT	8648986-8649017	32	NZ_CP050647	Escherichia coli strain PapM-36-2 plasmid pIncFIB, complete sequence	18910-18941	7	0.781
NZ_CP022203_17	17.1\|8648986\|32\|NZ_CP022203\|PILER-CR,CRISPRCasFinder,CRT	8648986-8649017	32	NZ_CP010126	Escherichia coli strain C8 plasmid A, complete genome	12534-12565	7	0.781
NZ_CP022203_17	17.1\|8648986\|32\|NZ_CP022203\|PILER-CR,CRISPRCasFinder,CRT	8648986-8649017	32	NZ_CP031323	Escherichia coli strain ST2350 isolate Es_ST2350_SE1_NDM_03_2018 plasmid pEsST2350_SE_2, complete sequence	4792-4823	7	0.781
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NZ_CP041045	Paracoccus sp. AK26 plasmid pAK1, complete sequence	8935-8967	7	0.788
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NZ_CP044425	Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence	107556-107588	7	0.788
NZ_CP022203_18	18.50\|8682100\|33\|NZ_CP022203\|PILER-CR	8682100-8682132	33	NZ_LR723678	Arsenite-oxidising bacterium NT-25 plasmid 2	47504-47536	7	0.788
NZ_CP022203_18	18.50\|8682100\|33\|NZ_CP022203\|PILER-CR	8682100-8682132	33	NZ_FO082821	Rhizobium sp. NT-26 plasmid NT26_p1, complete sequence	128725-128757	7	0.788
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NZ_CP041045	Paracoccus sp. AK26 plasmid pAK1, complete sequence	8935-8967	7	0.788
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NZ_CP044425	Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence	107556-107588	7	0.788
NZ_CP022203_18	18.100\|8682097\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8682097-8682129	33	NZ_LR723678	Arsenite-oxidising bacterium NT-25 plasmid 2	47504-47536	7	0.788
NZ_CP022203_18	18.100\|8682097\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8682097-8682129	33	NZ_FO082821	Rhizobium sp. NT-26 plasmid NT26_p1, complete sequence	128725-128757	7	0.788
NZ_CP022203_19	19.1\|8817623\|40\|NZ_CP022203\|CRISPRCasFinder	8817623-8817662	40	NZ_CP029831	Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence	343401-343440	7	0.825
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	1649103-1649133	8	0.742
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NZ_CP023071	Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence	1625565-1625595	8	0.742
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NZ_CP029232	Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence	377538-377568	8	0.742
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NZ_CP031166	Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence	542418-542448	8	0.742
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_LR134465	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence	147282-147315	8	0.765
NZ_CP022203_11	11.4\|5516783\|33\|NZ_CP022203\|CRT	5516783-5516815	33	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1069823-1069855	8	0.758
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NC_010578	Beijerinckia indica subsp. indica ATCC 9039 plasmid pBIND02, complete sequence	49274-49303	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NZ_CP016083	Streptomyces sp. SAT1 plasmid unnamed3, complete sequence	139457-139486	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	423177-423206	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1460154-1460183	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	353108-353137	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NZ_CP019484	Sinorhizobium meliloti strain B401 plasmid pSymB, complete sequence	674667-674696	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NZ_CP019487	Sinorhizobium meliloti strain B399 plasmid pSym, complete sequence	463353-463382	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	MK967402	Mycobacterium phage NihilNomen, complete genome	79485-79514	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	MH727551	Mycobacterium phage Kalah2, complete genome	79732-79761	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	JN116822	Rhodococcus phage RRH1, complete genome	13831-13860	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NC_014458	Mycobacterium phage Angelica, complete genome	3434-3463	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	MG962364	Mycobacterium phage Deby, complete genome	3434-3463	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	MK524527	Mycobacterium phage ThreeRngTarjay, complete genome	80556-80585	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	MK524529	Mycobacterium phage Phoebus, complete genome	81965-81994	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	MF919532	Mycobacterium phage Sulley, complete genome	3434-3463	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	KF114875	Mycobacterium phage Redno2, complete genome	77487-77516	8	0.733
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	MK524504	Mycobacterium phage Hughesyang, complete genome	80611-80640	8	0.733
NZ_CP022203_12	12.1\|6778349\|30\|NZ_CP022203\|PILER-CR	6778349-6778378	30	NC_010070	Burkholderia multivorans ATCC 17616 plasmid pBMUL01, complete sequence	111297-111326	8	0.733
NZ_CP022203_12	12.1\|6778349\|30\|NZ_CP022203\|PILER-CR	6778349-6778378	30	NC_010802	Burkholderia multivorans ATCC 17616 plasmid pTGL1, complete sequence	2160-2189	8	0.733
NZ_CP022203_16	16.27\|8645110\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8645110-8645143	34	MN034385	Leviviridae sp. isolate H2_Rhizo_31_scaffold_518 hypothetical protein (H2Rhizo31518_000001) gene, partial cds; and hypothetical protein (H2Rhizo31518_000002), RNA-dependent RNA polymerase (H2Rhizo31518_000003), and hypothetical protein (H2Rhizo31518_000004) genes, complete cds	3264-3297	8	0.765
NZ_CP022203_16	16.27\|8645110\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8645110-8645143	34	MN035339	Leviviridae sp. isolate H2_Rhizo_33_scaffold_3580 sequence	1476-1509	8	0.765
NZ_CP022203_16	16.27\|8645110\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8645110-8645143	34	MN035781	Leviviridae sp. isolate H4_Bulk_47_scaffold_337 hypothetical protein (H4Bulk47337_000001) gene, partial cds; and hypothetical protein (H4Bulk47337_000002), RNA-dependent RNA polymerase (H4Bulk47337_000003), and hypothetical protein (H4Bulk47337_000004) genes, complete cds	3264-3297	8	0.765
NZ_CP022203_16	16.46\|8646468\|33\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646468-8646500	33	NZ_CP027859	Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence	1427420-1427452	8	0.758
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	MK494123	Mycobacterium phage Blackbeetle, complete genome	6803-6836	8	0.765
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	MG757167	Mycobacterium phage Tesla, complete genome	6794-6827	8	0.765
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	MK305892	Mycobacterium phage RedRaider77, complete genome	6942-6975	8	0.765
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	KJ538721	Mycobacterium phage MosMoris, complete genome	6692-6725	8	0.765
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	MN329676	Mycobacterium phage Poise, complete genome	6803-6836	8	0.765
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	KX159477	Mycobacterium phage Gattaca, complete genome	6692-6725	8	0.765
NZ_CP022203_17	17.1\|8648986\|32\|NZ_CP022203\|PILER-CR,CRISPRCasFinder,CRT	8648986-8649017	32	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	759035-759066	8	0.75
NZ_CP022203_18	18.25\|8680307\|35\|NZ_CP022203\|PILER-CR	8680307-8680341	35	NC_023722	Rhodococcus phage ReqiPine5, complete genome	3580-3614	8	0.771
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	JN106171	Uncultured bacterium plasmid pAKD26, complete sequence	31212-31245	8	0.765
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NZ_CP013369	Burkholderia ubonensis strain RF23-BP41 plasmid pRF23, complete sequence	143541-143574	8	0.765
NZ_CP022203_18	18.30\|8680665\|33\|NZ_CP022203\|PILER-CR	8680665-8680697	33	NC_016817	Pantoea ananatis LMG 5342 plasmid pPANA10, complete sequence	122751-122783	8	0.758
NZ_CP022203_18	18.30\|8680665\|33\|NZ_CP022203\|PILER-CR	8680665-8680697	33	NZ_CP020944	Pantoea ananatis strain PNA 97-1R plasmid unamed1, complete sequence	122816-122848	8	0.758
NZ_CP022203_18	18.30\|8680665\|33\|NZ_CP022203\|PILER-CR	8680665-8680697	33	NC_017553	Pantoea ananatis PA13 plasmid PAGR_p, complete sequence	122905-122937	8	0.758
NZ_CP022203_18	18.30\|8680665\|33\|NZ_CP022203\|PILER-CR	8680665-8680697	33	NZ_CP022429	Pantoea ananatis strain YJ76 plasmid p_unamed1	241652-241684	8	0.758
NZ_CP022203_18	18.30\|8680665\|33\|NZ_CP022203\|PILER-CR	8680665-8680697	33	NC_017533	Pantoea ananatis AJ13355 plasmid pEA320, complete sequence	309620-309652	8	0.758
NZ_CP022203_18	18.30\|8680665\|33\|NZ_CP022203\|PILER-CR	8680665-8680697	33	NZ_CP014208	Pantoea ananatis strain R100 plasmid, complete sequence	254763-254795	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH271319	Rhodococcus UhSalsa, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MF324902	Rhodococcus phage Krishelle, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	KT959213	Rhodococcus phage TWAMP, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH271297	Rhodococcus phage Erik, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH271309	Rhodococcus phage Phrankenstein, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MF324904	Rhodococcus phage RexFury, complete genome	5108-5140	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MF324901	Rhodococcus phage Naiad, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	KT990218	Rhodococcus phage Lillie, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	KX550082	Rhodococcus phage Natosaleda, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MK524495	Rhodococcus phage Belenaria, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH271299	Rhodococcus phage Gollum, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH271293	Rhodococcus phage Bradshaw, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NC_028677	Rhodococcus phage CosmicSans, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH271306	Rhodococcus phage Nancinator, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH271314	Rhodococcus phage Swann, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MF324900	Rhodococcus phage StCroix, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH316569	Rhodococcus phage Shuman, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	KT375356	Rhodococcus phage Rhodalysa, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MK524487	Rhodococcus phage Espica, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NC_016653	Rhodococcus phage RER2, complete genome	1949-1981	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MF324905	Rhodococcus phage Alatin, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NZ_AP019795	Thermus thermophilus strain AA2-29 plasmid pAA229, complete sequence	55435-55467	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	59033-59065	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NZ_AP019793	Thermus thermophilus strain AA2-20 plasmid pAA220, complete sequence	80621-80653	8	0.758
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	MH047631	Microbacterium phage Triscuit, complete genome	35138-35170	8	0.758
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_010158	Yersinia pestis Angola plasmid pMT-pPCP, complete sequence	76258-76289	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_015382	Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence	188318-188349	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_005815	Yersinia pestis biovar Microtus str. 91001 plasmid pMT1, complete sequence	2462-2493	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009490	Yersinia pestis strain PBM19 plasmid pMT1, complete sequence	87396-87427	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009714	Yersinia pestis Pestoides F plasmid pMT, complete sequence	131740-131771	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009702	Yersinia pestis strain Harbin35 plasmid unnamed1, complete sequence	53130-53161	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009784	Yersinia pestis strain El Dorado plasmid pMT, complete sequence	11909-11940	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009722	Yersinia pestis strain Shasta plasmid pMT, complete sequence	73791-73822	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP045259	Yersinia pestis strain SCPM-O-B-5942 (I-2638) plasmid pMT, complete sequence	56899-56930	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_014022	Yersinia pestis Z176003 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_017266	Yersinia pestis biovar Medievalis str. Harbin 35 plasmid pMT, complete sequence	2462-2493	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP033694	Yersinia pestis strain FDAARGOS_602 plasmid unnamed1, complete sequence	73116-73147	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_009378	Yersinia pestis Pestoides F plasmid MT, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP033700	Yersinia pestis strain FDAARGOS_601 plasmid unnamed3	87259-87290	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP033700	Yersinia pestis strain FDAARGOS_601 plasmid unnamed3	122784-122815	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_006323	Yersinia pestis plasmid pG8786, complete sequence	519-550	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP045146	Yersinia pestis strain SCPM-O-B-6899 (231) plasmid pMT, complete sequence	56894-56925	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP045164	Yersinia pestis strain SCPM-O-B-6291 (C-25) plasmid pMT, complete sequence	56900-56931	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP045155	Yersinia pestis strain SCPM-O-B-5935 (I-1996) plasmid pMT, complete sequence	56895-56926	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP045159	Yersinia pestis subsp. pestis bv. Medievalis strain SCPM-O-B-6530 plasmid pMT, complete sequence	57610-57641	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP006746	Yersinia pestis 8787 plasmid pMT1, complete sequence	48571-48602	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_003134	Yersinia pestis CO92 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP045150	Yersinia pestis strain SCPM-O-DNA-18 (I-3113) plasmid pMT, complete sequence	56899-56930	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP006790	Yersinia pestis 2944 plasmid pMT, complete sequence	45610-45641	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP006749	Yersinia pestis 3770 plasmid pMT1, complete sequence	44900-44931	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP006756	Yersinia pestis 1522 plasmid pMT, complete sequence	88413-88444	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_017155	Yersinia pestis D106004 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_017158	Yersinia pestis D182038 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_004835	Yersinia pestis strain KIM5 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_004838	Yersinia pestis KIM10+ plasmid pMT-1, complete sequence	45840-45871	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP033692	Yersinia pestis strain FDAARGOS_603 plasmid unnamed3, complete sequence	47045-47076	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP033693	Yersinia pestis strain FDAARGOS_603 plasmid unnamed4	2103-2134	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP033693	Yersinia pestis strain FDAARGOS_603 plasmid unnamed4	103753-103784	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP006760	Yersinia pestis 1413 plasmid pMT, complete sequence	48571-48602	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP006779	Yersinia pestis 1412 plasmid pMT, complete sequence	3897-3928	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP006752	Yersinia pestis 3067 plasmid pMT1, complete sequence	66666-66697	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NC_008118	Yersinia pestis Nepal516 plasmid pMT, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP016275	Yersinia pestis strain Cadman plasmid pMT1, complete sequence	79599-79630	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP019709	Yersinia pestis strain 195/P plasmid pMT1, complete sequence	11475-11506	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009904	Yersinia pestis Antiqua plasmid pMT, complete sequence	43672-43703	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009841	Yersinia pestis A1122 plasmid pMT, complete sequence	40033-40064	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009989	Yersinia pestis strain Nicholisk 41 plasmid 1, complete sequence	17837-17868	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP009934	Yersinia pestis Angola plasmid pMT, complete sequence	16201-16232	8	0.75
NZ_CP022203_18	18.47\|8681889\|32\|NZ_CP022203\|PILER-CR	8681889-8681920	32	NZ_CP010021	Yersinia pestis str. Pestoides B plasmid pMT, complete sequence	97766-97797	8	0.75
NZ_CP022203_18	18.75\|8680304\|35\|NZ_CP022203\|CRISPRCasFinder,CRT	8680304-8680338	35	NC_023722	Rhodococcus phage ReqiPine5, complete genome	3580-3614	8	0.771
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	JN106171	Uncultured bacterium plasmid pAKD26, complete sequence	31212-31245	8	0.765
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NZ_CP013369	Burkholderia ubonensis strain RF23-BP41 plasmid pRF23, complete sequence	143541-143574	8	0.765
NZ_CP022203_18	18.80\|8680662\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680662-8680694	33	NC_016817	Pantoea ananatis LMG 5342 plasmid pPANA10, complete sequence	122751-122783	8	0.758
NZ_CP022203_18	18.80\|8680662\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680662-8680694	33	NZ_CP020944	Pantoea ananatis strain PNA 97-1R plasmid unamed1, complete sequence	122816-122848	8	0.758
NZ_CP022203_18	18.80\|8680662\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680662-8680694	33	NC_017553	Pantoea ananatis PA13 plasmid PAGR_p, complete sequence	122905-122937	8	0.758
NZ_CP022203_18	18.80\|8680662\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680662-8680694	33	NZ_CP022429	Pantoea ananatis strain YJ76 plasmid p_unamed1	241652-241684	8	0.758
NZ_CP022203_18	18.80\|8680662\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680662-8680694	33	NC_017533	Pantoea ananatis AJ13355 plasmid pEA320, complete sequence	309620-309652	8	0.758
NZ_CP022203_18	18.80\|8680662\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680662-8680694	33	NZ_CP014208	Pantoea ananatis strain R100 plasmid, complete sequence	254763-254795	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH271319	Rhodococcus UhSalsa, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MF324902	Rhodococcus phage Krishelle, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	KT959213	Rhodococcus phage TWAMP, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH271297	Rhodococcus phage Erik, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH271309	Rhodococcus phage Phrankenstein, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MF324904	Rhodococcus phage RexFury, complete genome	5108-5140	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MF324901	Rhodococcus phage Naiad, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	KT990218	Rhodococcus phage Lillie, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	KX550082	Rhodococcus phage Natosaleda, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MK524495	Rhodococcus phage Belenaria, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH271299	Rhodococcus phage Gollum, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH271293	Rhodococcus phage Bradshaw, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NC_028677	Rhodococcus phage CosmicSans, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH271306	Rhodococcus phage Nancinator, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH271314	Rhodococcus phage Swann, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MF324900	Rhodococcus phage StCroix, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH316569	Rhodococcus phage Shuman, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	KT375356	Rhodococcus phage Rhodalysa, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MK524487	Rhodococcus phage Espica, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NC_016653	Rhodococcus phage RER2, complete genome	1949-1981	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MF324905	Rhodococcus phage Alatin, complete genome	5077-5109	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NZ_AP019795	Thermus thermophilus strain AA2-29 plasmid pAA229, complete sequence	55435-55467	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	59033-59065	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NZ_AP019793	Thermus thermophilus strain AA2-20 plasmid pAA220, complete sequence	80621-80653	8	0.758
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	MH047631	Microbacterium phage Triscuit, complete genome	35138-35170	8	0.758
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_010158	Yersinia pestis Angola plasmid pMT-pPCP, complete sequence	76258-76289	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_015382	Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence	188318-188349	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_005815	Yersinia pestis biovar Microtus str. 91001 plasmid pMT1, complete sequence	2462-2493	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009490	Yersinia pestis strain PBM19 plasmid pMT1, complete sequence	87396-87427	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009714	Yersinia pestis Pestoides F plasmid pMT, complete sequence	131740-131771	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009702	Yersinia pestis strain Harbin35 plasmid unnamed1, complete sequence	53130-53161	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009784	Yersinia pestis strain El Dorado plasmid pMT, complete sequence	11909-11940	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009722	Yersinia pestis strain Shasta plasmid pMT, complete sequence	73791-73822	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP045259	Yersinia pestis strain SCPM-O-B-5942 (I-2638) plasmid pMT, complete sequence	56899-56930	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_014022	Yersinia pestis Z176003 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_017266	Yersinia pestis biovar Medievalis str. Harbin 35 plasmid pMT, complete sequence	2462-2493	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP033694	Yersinia pestis strain FDAARGOS_602 plasmid unnamed1, complete sequence	73116-73147	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_009378	Yersinia pestis Pestoides F plasmid MT, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP033700	Yersinia pestis strain FDAARGOS_601 plasmid unnamed3	87259-87290	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP033700	Yersinia pestis strain FDAARGOS_601 plasmid unnamed3	122784-122815	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_006323	Yersinia pestis plasmid pG8786, complete sequence	519-550	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP045146	Yersinia pestis strain SCPM-O-B-6899 (231) plasmid pMT, complete sequence	56894-56925	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP045164	Yersinia pestis strain SCPM-O-B-6291 (C-25) plasmid pMT, complete sequence	56900-56931	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP045155	Yersinia pestis strain SCPM-O-B-5935 (I-1996) plasmid pMT, complete sequence	56895-56926	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP045159	Yersinia pestis subsp. pestis bv. Medievalis strain SCPM-O-B-6530 plasmid pMT, complete sequence	57610-57641	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP006746	Yersinia pestis 8787 plasmid pMT1, complete sequence	48571-48602	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_003134	Yersinia pestis CO92 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP045150	Yersinia pestis strain SCPM-O-DNA-18 (I-3113) plasmid pMT, complete sequence	56899-56930	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP006790	Yersinia pestis 2944 plasmid pMT, complete sequence	45610-45641	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP006749	Yersinia pestis 3770 plasmid pMT1, complete sequence	44900-44931	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP006756	Yersinia pestis 1522 plasmid pMT, complete sequence	88413-88444	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_017155	Yersinia pestis D106004 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_017158	Yersinia pestis D182038 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_004835	Yersinia pestis strain KIM5 plasmid pMT1, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_004838	Yersinia pestis KIM10+ plasmid pMT-1, complete sequence	45840-45871	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP033692	Yersinia pestis strain FDAARGOS_603 plasmid unnamed3, complete sequence	47045-47076	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP033693	Yersinia pestis strain FDAARGOS_603 plasmid unnamed4	2103-2134	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP033693	Yersinia pestis strain FDAARGOS_603 plasmid unnamed4	103753-103784	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP006760	Yersinia pestis 1413 plasmid pMT, complete sequence	48571-48602	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP006779	Yersinia pestis 1412 plasmid pMT, complete sequence	3897-3928	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP006752	Yersinia pestis 3067 plasmid pMT1, complete sequence	66666-66697	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NC_008118	Yersinia pestis Nepal516 plasmid pMT, complete sequence	2466-2497	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP016275	Yersinia pestis strain Cadman plasmid pMT1, complete sequence	79599-79630	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP019709	Yersinia pestis strain 195/P plasmid pMT1, complete sequence	11475-11506	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009904	Yersinia pestis Antiqua plasmid pMT, complete sequence	43672-43703	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009841	Yersinia pestis A1122 plasmid pMT, complete sequence	40033-40064	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009989	Yersinia pestis strain Nicholisk 41 plasmid 1, complete sequence	17837-17868	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP009934	Yersinia pestis Angola plasmid pMT, complete sequence	16201-16232	8	0.75
NZ_CP022203_18	18.97\|8681886\|32\|NZ_CP022203\|CRISPRCasFinder,CRT	8681886-8681917	32	NZ_CP010021	Yersinia pestis str. Pestoides B plasmid pMT, complete sequence	97766-97797	8	0.75
NZ_CP022203_1	1.2\|31687\|31\|NZ_CP022203\|CRT	31687-31717	31	NZ_CP020572	Thermus aquaticus strain YT-1 plasmid p61, complete sequence	5767-5797	9	0.71
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP034087	Methylocystis rosea strain GW6 plasmid pGW6_1, complete sequence	266514-266547	9	0.735
NZ_CP022203_11	11.4\|5516783\|33\|NZ_CP022203\|CRT	5516783-5516815	33	NZ_CP020041	Streptomyces sp. 3211 isolate 3 plasmid p3211-2, complete sequence	166926-166958	9	0.727
NZ_CP022203_11	11.4\|5516783\|33\|NZ_CP022203\|CRT	5516783-5516815	33	NC_020894	Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence	156935-156967	9	0.727
NZ_CP022203_11	11.4\|5516783\|33\|NZ_CP022203\|CRT	5516783-5516815	33	NC_017766	Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence	156936-156968	9	0.727
NZ_CP022203_11	11.6\|5516873\|30\|NZ_CP022203\|CRT	5516873-5516902	30	NZ_CP037443	Klebsiella sp. PO552 plasmid p2, complete sequence	59450-59479	9	0.7
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NZ_CP015867	Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence	7854-7883	9	0.7
NZ_CP022203_11	11.8\|5516990\|30\|NZ_CP022203\|CRT	5516990-5517019	30	NZ_CP010990	Pseudonocardia sp. EC080625-04 plasmid pFRP1-1, complete sequence	25733-25762	9	0.7
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NC_010070	Burkholderia multivorans ATCC 17616 plasmid pBMUL01, complete sequence	143439-143472	9	0.735
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NZ_CP022369	Azospirillum sp. TSH58 plasmid TSH58_p05, complete sequence	52425-52458	9	0.735
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NZ_CP013108	Sinorhizobium americanum strain CFNEI 73 plasmid A, complete sequence	201633-201666	9	0.735
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NZ_CP028965	Burkholderia sp. IDO3 plasmid p1, complete sequence	79509-79542	9	0.735
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NZ_CP028965	Burkholderia sp. IDO3 plasmid p1, complete sequence	224775-224808	9	0.735
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NC_010802	Burkholderia multivorans ATCC 17616 plasmid pTGL1, complete sequence	137436-137469	9	0.735
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NZ_CP023408	Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence	240861-240894	9	0.735
NZ_CP022203_16	16.13\|8644114\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8644114-8644147	34	NZ_CP023039	Komagataeibacter saccharivorans strain CV1 plasmid unnamed3, complete sequence	12726-12759	9	0.735
NZ_CP022203_16	16.20\|8644612\|35\|NZ_CP022203\|CRISPRCasFinder,CRT	8644612-8644646	35	NC_021289	Burkholderia insecticola plasmid p1, complete sequence	239141-239175	9	0.743
NZ_CP022203_16	16.20\|8644612\|35\|NZ_CP022203\|CRISPRCasFinder,CRT	8644612-8644646	35	NZ_AP022319	Burkholderia sp. THE68 plasmid BTHE68_p1, complete sequence	1156380-1156414	9	0.743
NZ_CP022203_16	16.31\|8645391\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8645391-8645424	34	NZ_CP049911	Diaphorobacter sp. HDW4A plasmid p_unnamed1, complete sequence	108490-108523	9	0.735
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP012748	Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence	504209-504245	9	0.757
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	MK511056	Pseudomonas phage BR293, partial genome	9472-9508	9	0.757
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	MK511055	Pseudomonas phage BR204, partial genome	9484-9520	9	0.757
NZ_CP022203_16	16.50\|8646749\|33\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646749-8646781	33	NC_013857	Azospirillum sp. B510 plasmid pAB510c, complete sequence	522602-522634	9	0.727
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	NZ_CP027025	Streptomyces sp. WAC00288 plasmid p3, complete sequence	23636-23669	9	0.735
NZ_CP022203_16	16.56\|8647178\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8647178-8647211	34	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	981842-981875	9	0.735
NZ_CP022203_18	18.4\|8678788\|33\|NZ_CP022203\|PILER-CR,CRISPRCasFinder,CRT	8678788-8678820	33	NZ_CP013855	Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence	333382-333414	9	0.727
NZ_CP022203_18	18.4\|8678788\|33\|NZ_CP022203\|PILER-CR,CRISPRCasFinder,CRT	8678788-8678820	33	NZ_CP011869	Pseudonocardia sp. HH130629-09 plasmid pLS1-1, complete sequence	138667-138699	9	0.727
NZ_CP022203_18	18.17\|8679729\|33\|NZ_CP022203\|PILER-CR	8679729-8679761	33	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1104356-1104388	9	0.727
NZ_CP022203_18	18.17\|8679729\|33\|NZ_CP022203\|PILER-CR	8679729-8679761	33	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	708768-708800	9	0.727
NZ_CP022203_18	18.17\|8679729\|33\|NZ_CP022203\|PILER-CR	8679729-8679761	33	KY385381	Mycobacterium phage EniyanLRS, complete genome	1861-1893	9	0.727
NZ_CP022203_18	18.17\|8679729\|33\|NZ_CP022203\|PILER-CR	8679729-8679761	33	MN585992	Mycobacterium phage MaryV, complete genome	2318-2350	9	0.727
NZ_CP022203_18	18.17\|8679729\|33\|NZ_CP022203\|PILER-CR	8679729-8679761	33	NC_008206	Mycobacteriophage Wildcat, complete genome	2328-2360	9	0.727
NZ_CP022203_18	18.17\|8679729\|33\|NZ_CP022203\|PILER-CR	8679729-8679761	33	KP027195	Mycobacterium phage Cosmo, complete genome	2318-2350	9	0.727
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NZ_LR594660	Variovorax sp. PBL-H6 plasmid 2	521337-521370	9	0.735
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NZ_LR594667	Variovorax sp. SRS16 plasmid 2	314199-314232	9	0.735
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NC_008760	Polaromonas naphthalenivorans CJ2 plasmid pPNAP04, complete sequence	37943-37976	9	0.735
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NC_016968	Comamonas testosteroni plasmid pTB30, complete sequence	34377-34410	9	0.735
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NZ_LR594672	Variovorax sp. PBL-E5 plasmid 2	315398-315431	9	0.735
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NC_019263	Delftia acidovorans plasmid pLME1, complete sequence	34741-34774	9	0.735
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NC_008195	Mycobacterium phage Cooper, complete genome	26591-26623	9	0.727
NZ_CP022203_18	18.33\|8680885\|33\|NZ_CP022203\|PILER-CR	8680885-8680917	33	NZ_LR134468	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 26, complete sequence	5440-5472	9	0.727
NZ_CP022203_18	18.37\|8681173\|33\|NZ_CP022203\|PILER-CR	8681173-8681205	33	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1636490-1636522	9	0.727
NZ_CP022203_18	18.45\|8681749\|34\|NZ_CP022203\|PILER-CR	8681749-8681782	34	NZ_CP040821	Paraoceanicella profunda strain D4M1 plasmid pD4M1C, complete sequence	96957-96990	9	0.735
NZ_CP022203_18	18.46\|8681819\|34\|NZ_CP022203\|PILER-CR	8681819-8681852	34	MN234221	Arthrobacter phage Shepard, complete genome	8464-8497	9	0.735
NZ_CP022203_18	18.52\|8682241\|36\|NZ_CP022203\|PILER-CR	8682241-8682276	36	KC661275	Mycobacterium phage HINdeR, complete genome	50606-50641	9	0.75
NZ_CP022203_18	18.67\|8679726\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8679726-8679758	33	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1104356-1104388	9	0.727
NZ_CP022203_18	18.67\|8679726\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8679726-8679758	33	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	708768-708800	9	0.727
NZ_CP022203_18	18.67\|8679726\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8679726-8679758	33	KY385381	Mycobacterium phage EniyanLRS, complete genome	1861-1893	9	0.727
NZ_CP022203_18	18.67\|8679726\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8679726-8679758	33	MN585992	Mycobacterium phage MaryV, complete genome	2318-2350	9	0.727
NZ_CP022203_18	18.67\|8679726\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8679726-8679758	33	NC_008206	Mycobacteriophage Wildcat, complete genome	2328-2360	9	0.727
NZ_CP022203_18	18.67\|8679726\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8679726-8679758	33	KP027195	Mycobacterium phage Cosmo, complete genome	2318-2350	9	0.727
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NZ_LR594660	Variovorax sp. PBL-H6 plasmid 2	521337-521370	9	0.735
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NZ_LR594667	Variovorax sp. SRS16 plasmid 2	314199-314232	9	0.735
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NC_008760	Polaromonas naphthalenivorans CJ2 plasmid pPNAP04, complete sequence	37943-37976	9	0.735
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NC_016968	Comamonas testosteroni plasmid pTB30, complete sequence	34377-34410	9	0.735
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NZ_LR594672	Variovorax sp. PBL-E5 plasmid 2	315398-315431	9	0.735
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NC_019263	Delftia acidovorans plasmid pLME1, complete sequence	34741-34774	9	0.735
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NC_008195	Mycobacterium phage Cooper, complete genome	26591-26623	9	0.727
NZ_CP022203_18	18.83\|8680882\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8680882-8680914	33	NZ_LR134468	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 26, complete sequence	5440-5472	9	0.727
NZ_CP022203_18	18.87\|8681170\|33\|NZ_CP022203\|CRISPRCasFinder,CRT	8681170-8681202	33	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1636490-1636522	9	0.727
NZ_CP022203_18	18.95\|8681746\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8681746-8681779	34	NZ_CP040821	Paraoceanicella profunda strain D4M1 plasmid pD4M1C, complete sequence	96957-96990	9	0.735
NZ_CP022203_18	18.96\|8681816\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8681816-8681849	34	MN234221	Arthrobacter phage Shepard, complete genome	8464-8497	9	0.735
NZ_CP022203_18	18.102\|8682238\|36\|NZ_CP022203\|CRISPRCasFinder,CRT	8682238-8682273	36	KC661275	Mycobacterium phage HINdeR, complete genome	50606-50641	9	0.75
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1646608-1646641	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP021653	Ralstonia solanacearum strain RS 488 plasmid unnamed, complete sequence	1601492-1601525	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP021767	Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence	1601505-1601538	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP012940	Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence	1324412-1324445	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP012944	Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence	519836-519869	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP012688	Ralstonia solanacearum strain UY031 plasmid unnamed, complete sequence	1601490-1601523	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NC_017575	Ralstonia solanacearum Po82 megaplasmid, complete sequence	863895-863928	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP026308	Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence	863873-863906	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	CP047139	Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence	1507973-1508006	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	NZ_CP051295	Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence	1309989-1310022	10	0.706
NZ_CP022203_1	1.3\|31744\|34\|NZ_CP022203\|CRT	31744-31777	34	CP047137	Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence	1451914-1451947	10	0.706
NZ_CP022203_16	16.28\|8645180\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8645180-8645214	35	NZ_CP040722	Rhodococcus pyridinivorans strain YF3 plasmid unnamed3, complete sequence	80909-80943	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP048224	Aeromonas salmonicida subsp. salmonicida strain J223 plasmid pASal5, complete sequence	42512-42546	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP017144	Aeromonas salmonicida subsp. masoucida strain RFAS1 plasmid unnamed1, complete sequence	27119-27153	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP022171	Aeromonas salmonicida strain S121 plasmid pS121-2, complete sequence	40297-40331	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP022182	Aeromonas salmonicida strain S68 plasmid pS68-1, complete sequence	18935-18969	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NC_009350	Aeromonas salmonicida subsp. salmonicida A449 plasmid 5, complete sequence	44010-44044	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP038103	Aeromonas salmonicida subsp. salmonicida strain SHY16-3432 plasmid pAsa5-3432, complete sequence	46606-46640	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP038104	Aeromonas salmonicida subsp. salmonicida strain SHY16-3432 plasmid pAsa9-like, complete sequence	26478-26512	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP022177	Aeromonas salmonicida strain S44 plasmid pS44-2, complete sequence	37722-37756	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_KY555070	Aeromonas salmonicida subsp. salmonicida strain 01-B526 plasmid pAsa9, complete sequence	26469-26503	10	0.714
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_KY555069	Aeromonas salmonicida subsp. salmonicida strain 01-B526 plasmid pAsa5, complete sequence	46636-46670	10	0.714
NZ_CP022203_16	16.42\|8646183\|33\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646183-8646215	33	KY709687	Salmonella phage 29485, complete genome	35148-35180	10	0.697
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP013104	Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence	185319-185355	10	0.73
NZ_CP022203_16	16.45\|8646397\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646397-8646431	35	NZ_CP045120	Rubrobacter sp. SCSIO 52909 plasmid unnamed1, complete sequence	130736-130770	10	0.714
NZ_CP022203_16	16.45\|8646397\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646397-8646431	35	KC292026	Halovirus HGTV-1, complete genome	19739-19773	10	0.714
NZ_CP022203_18	18.28\|8680522\|34\|NZ_CP022203\|PILER-CR	8680522-8680555	34	NC_029005	Streptomyces phage phiSAJS1, complete genome	32154-32187	10	0.706
NZ_CP022203_18	18.43\|8681606\|37\|NZ_CP022203\|PILER-CR	8681606-8681642	37	NZ_CP010024	Paraburkholderia fungorum strain ATCC BAA-463 plasmid pBIL, complete sequence	222527-222563	10	0.73
NZ_CP022203_18	18.54\|8682383\|34\|NZ_CP022203\|PILER-CR	8682383-8682416	34	NZ_KY349138	Mycolicibacterium sp. CBMA 213 plasmid pCBMA213_2, complete sequence	124497-124530	10	0.706
NZ_CP022203_18	18.62\|8682952\|34\|NZ_CP022203\|PILER-CR	8682952-8682985	34	NZ_CP013739	Streptomyces globisporus C-1027 plasmid SGLP1, complete sequence	57226-57259	10	0.706
NZ_CP022203_18	18.78\|8680519\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8680519-8680552	34	NC_029005	Streptomyces phage phiSAJS1, complete genome	32154-32187	10	0.706
NZ_CP022203_18	18.93\|8681603\|37\|NZ_CP022203\|CRISPRCasFinder,CRT	8681603-8681639	37	NZ_CP010024	Paraburkholderia fungorum strain ATCC BAA-463 plasmid pBIL, complete sequence	222527-222563	10	0.73
NZ_CP022203_18	18.104\|8682380\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8682380-8682413	34	NZ_KY349138	Mycolicibacterium sp. CBMA 213 plasmid pCBMA213_2, complete sequence	124497-124530	10	0.706
NZ_CP022203_18	18.112\|8682949\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8682949-8682982	34	NZ_CP013739	Streptomyces globisporus C-1027 plasmid SGLP1, complete sequence	57226-57259	10	0.706
NZ_CP022203_16	16.3\|8643387\|35\|NZ_CP022203\|CRISPRCasFinder,CRT	8643387-8643421	35	MG696115	Plesiomonas phage phiP4-7, complete genome	37164-37198	11	0.686
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP048224	Aeromonas salmonicida subsp. salmonicida strain J223 plasmid pASal5, complete sequence	121898-121932	11	0.686
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NC_009350	Aeromonas salmonicida subsp. salmonicida A449 plasmid 5, complete sequence	122384-122418	11	0.686
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_CP038103	Aeromonas salmonicida subsp. salmonicida strain SHY16-3432 plasmid pAsa5-3432, complete sequence	147315-147349	11	0.686
NZ_CP022203_16	16.40\|8646034\|35\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646034-8646068	35	NZ_KY555069	Aeromonas salmonicida subsp. salmonicida strain 01-B526 plasmid pAsa5, complete sequence	125024-125058	11	0.686
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP021653	Ralstonia solanacearum strain RS 488 plasmid unnamed, complete sequence	1483389-1483425	11	0.703
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP039340	Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence	1431498-1431534	11	0.703
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP012688	Ralstonia solanacearum strain UY031 plasmid unnamed, complete sequence	1483396-1483432	11	0.703
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	CP047139	Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence	1393632-1393668	11	0.703
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	CP047137	Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence	1338904-1338940	11	0.703
NZ_CP022203_18	18.45\|8681749\|34\|NZ_CP022203\|PILER-CR	8681749-8681782	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	212787-212820	11	0.676
NZ_CP022203_18	18.45\|8681749\|34\|NZ_CP022203\|PILER-CR	8681749-8681782	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	896286-896319	11	0.676
NZ_CP022203_18	18.45\|8681749\|34\|NZ_CP022203\|PILER-CR	8681749-8681782	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	916703-916736	11	0.676
NZ_CP022203_18	18.53\|8682313\|34\|NZ_CP022203\|PILER-CR	8682313-8682346	34	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	1425978-1426011	11	0.676
NZ_CP022203_18	18.53\|8682313\|34\|NZ_CP022203\|PILER-CR	8682313-8682346	34	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	211533-211566	11	0.676
NZ_CP022203_18	18.95\|8681746\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8681746-8681779	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	212787-212820	11	0.676
NZ_CP022203_18	18.95\|8681746\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8681746-8681779	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	896286-896319	11	0.676
NZ_CP022203_18	18.95\|8681746\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8681746-8681779	34	NZ_CP030772	Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence	916703-916736	11	0.676
NZ_CP022203_18	18.103\|8682310\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8682310-8682343	34	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	1425978-1426011	11	0.676
NZ_CP022203_18	18.103\|8682310\|34\|NZ_CP022203\|CRISPRCasFinder,CRT	8682310-8682343	34	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	211533-211566	11	0.676
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP026091	Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence	963549-963585	12	0.676
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NC_014309	Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome	1536216-1536252	12	0.676
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP026093	Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence	963647-963683	12	0.676
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP021767	Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence	1483343-1483379	12	0.676
NZ_CP022203_16	16.44\|8646324\|37\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646324-8646360	37	NZ_CP021765	Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence	1476960-1476996	12	0.676
NZ_CP022203_16	16.47\|8646537\|34\|NZ_CP022203\|CRISPRCasFinder,CRT,PILER-CR	8646537-8646570	34	NZ_CP018573	Marivivens sp. JLT3646 plasmid unnamed, complete sequence	123040-123073	12	0.647
NZ_CP022203_11	11.9\|5517038\|27\|NZ_CP022203\|CRT	5517038-5517064	27	NC_011887	Methylobacterium nodulans ORS 2060 plasmid pMNOD02, complete sequence	260754-260780	14	0.481

1. spacer 8.4|4795962|23|NZ_CP022203|CRT matches to NZ_CP054613 (Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence) position: , mismatch: 2, identity: 0.913

atgatgccgccgtcctcttcacc	CRISPR spacer
atgatgccgccgacctcttcagc	Protospacer
************ ******** *

2. spacer 9.2|5086336|22|NZ_CP022203|CRT matches to LN997845 (Streptomyces reticuli genome assembly TUE45, plasmid : IV) position: , mismatch: 2, identity: 0.909

cgcggcaccggcctcaccggca	CRISPR spacer
ggcggcaccggccgcaccggca	Protospacer
 ************ ********

3. spacer 9.2|5086336|22|NZ_CP022203|CRT matches to LR743530 (Xanthomonas phage Suba genome assembly, chromosome: 1) position: , mismatch: 2, identity: 0.909

cgcggcaccggcctcaccggca	CRISPR spacer
cgcggcaccggccttaccggcg	Protospacer
**************.******.

4. spacer 9.2|5086336|22|NZ_CP022203|CRT matches to MN586047 (Gordonia phage EMoore, complete genome) position: , mismatch: 2, identity: 0.909

cgcggcaccggcctcaccggca	CRISPR spacer
cgcggcaccggcgtcaccggcg	Protospacer
************ ********.

5. spacer 9.3|5086381|22|NZ_CP022203|CRT matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 2, identity: 0.909

ggcctcacccggagccgctgcg	CRISPR spacer
ggcctcacccgcagccgctgca	Protospacer
*********** *********.

6. spacer 4.1|2964279|25|NZ_CP022203|CRISPRCasFinder matches to MT536174 (Stenotrophomonas phage vB_SmaS-AXL_3, complete genome) position: , mismatch: 3, identity: 0.88

gatgcccgggtcgttggtctcgccg	CRISPR spacer
gatgcccgggtcgttgttgtcgctg	Protospacer
**************** * ****.*

7. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP027299 (Streptomyces sp. SGAir0924 plasmid unnamed_5) position: , mismatch: 3, identity: 0.889

ggacg-ggcgcccggcggcacggcgcca	CRISPR spacer
-gacgtggcgcccggcgccacggcgccc	Protospacer
 **** *********** *********

8. spacer 4.1|2964279|25|NZ_CP022203|CRISPRCasFinder matches to NZ_CP029834 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed4, complete sequence) position: , mismatch: 4, identity: 0.84

gatgcccgggtcgttggtctcgccg	CRISPR spacer
gatgaccgggtcgttggcctcgcgc	Protospacer
**** ************.*****

9. spacer 4.1|2964279|25|NZ_CP022203|CRISPRCasFinder matches to NZ_CP054617 (Azospirillum oryzae strain KACC 14407 plasmid unnamed3, complete sequence) position: , mismatch: 4, identity: 0.84

gatgcccgggtcgttggtctcgccg	CRISPR spacer
gatgaccgggtcgttggcctcgcgc	Protospacer
**** ************.*****

10. spacer 8.2|4795878|26|NZ_CP022203|CRT matches to NZ_CP020331 (Martelella mediterranea DSM 17316 strain MACL11 plasmid pMM593, complete sequence) position: , mismatch: 4, identity: 0.846

atgatgatgccgccgtcctcttcacc	CRISPR spacer
atgctgatgccgccgtcctcgtcgcg	Protospacer
*** **************** **.*

11. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP029358 (Azospirillum sp. CFH 70021 plasmid unnamed3) position: , mismatch: 4, identity: 0.852

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
agacgggcgaccggctgcacggcgccc	Protospacer
.******** ***** **********

12. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP032348 (Azospirillum brasilense strain MTCC4039 plasmid p4, complete sequence) position: , mismatch: 4, identity: 0.852

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
agacgggcgcccggcggccgggcgccc	Protospacer
.*****************  ******

13. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 4, identity: 0.852

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
ggcggggcgcccggcggcacggccccg	Protospacer
**  ******************* **.

14. spacer 4.1|2964279|25|NZ_CP022203|CRISPRCasFinder matches to NZ_CP034431 (Bradyrhizobium sp. LCT2 plasmid pLCT2, complete sequence) position: , mismatch: 5, identity: 0.8

gatgcccgggtcgttggtctcgccg	CRISPR spacer
cggccccgggtcgttggtctcgcgg	Protospacer
 .  ******************* *

15. spacer 8.2|4795878|26|NZ_CP022203|CRT matches to NZ_CP054613 (Paenibacillus cellulosilyticus strain KACC 14175 plasmid unnamed4, complete sequence) position: , mismatch: 5, identity: 0.808

atgatgatgccgccgtcctcttcacc	CRISPR spacer
tgcatgatgccgccgacctcttcagc	Protospacer
   ************ ******** *

16. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 5, identity: 0.833

gcgcccggggcgcccggaggcggcatgccg-	CRISPR spacer
gcgcccgcggcgcccggcggcggcg-gcggt	Protospacer
******* ********* ******. ** *

17. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP012944 (Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
gtggccgtggcgcccggcggcggcatgctg	Protospacer
*.* *** ********* **********.*

18. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP012940 (Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
gtggccgtggcgcccggcggcggcatgctg	Protospacer
*.* *** ********* **********.*

19. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NC_017575 (Ralstonia solanacearum Po82 megaplasmid, complete sequence) position: , mismatch: 5, identity: 0.833

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
gtggccgtggcgcccggcggcggcatgctg	Protospacer
*.* *** ********* **********.*

20. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP026308 (Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.833

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
gtggccgtggcgcccggcggcggcatgctg	Protospacer
*.* *** ********* **********.*

21. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP051295 (Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence) position: , mismatch: 5, identity: 0.833

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
gtggccgtggcgcccggcggcggcatgctg	Protospacer
*.* *** ********* **********.*

22. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NZ_CP029830 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed1, complete sequence) position: , mismatch: 5, identity: 0.833

acgcccggccccggcggaa--cccccggacgg	CRISPR spacer
tcgcccggccccggcggaacgccccttgac--	Protospacer
 ******************  ****. ***

23. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NC_011961 (Thermomicrobium roseum DSM 5159 plasmid unnamed, complete sequence) position: , mismatch: 5, identity: 0.815

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
caccgggctcctggcggcacggcgcca	Protospacer
 . ***** **.***************

24. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 5, identity: 0.815

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
ggcacggcgcccggcggcacggcgcgg	Protospacer
**   ******************** .

25. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 5, identity: 0.815

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
aaacgggcgcccggcgccacggcctca	Protospacer
..************** ****** .**

26. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP032054 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL1, complete sequence) position: , mismatch: 5, identity: 0.815

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
ggcacggcgcccggcggcacggcgcgg	Protospacer
**   ******************** .

27. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP016560 (Streptomyces clavuligerus strain F613-1 plasmid pSCL4, complete sequence) position: , mismatch: 5, identity: 0.815

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
ggcacggcgcccggcggcacggcgcgg	Protospacer
**   ******************** .

28. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 5, identity: 0.815

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
agcggggcgcccggcggcacgacggca	Protospacer
.*  *****************.** **

29. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_CP022417 (Sulfitobacter pseudonitzschiae strain SMR1 plasmid pSMR1-2, complete sequence) position: , mismatch: 5, identity: 0.815

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
ggacgggcgcccgtcggcagggctgaa	Protospacer
************* ***** ***   *

30. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to NZ_CP035514 (Haematobacter massiliensis strain OT1 plasmid pOT1-4, complete sequence) position: , mismatch: 5, identity: 0.815

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
cttgtccgggtccgtgaccagcgcacc	Protospacer
 ****.********** ******** .

31. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to NZ_CP025810 (Sulfitobacter sp. SK025 plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.815

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
gttgttcgggtccatgccctgcgcctc	Protospacer
*************.***** ****  .

32. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to NZ_CP044976 (Hydrogenophaga sp. PBL-H3 substr. PBL-H3(B2) plasmid pPBL-H3_B2-1, complete sequence) position: , mismatch: 5, identity: 0.815

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
tgtgttcgagtccgtggccagcgcact	Protospacer
  ******.******* ******** *

33. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 6, identity: 0.806

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
tcacggtcgcctggccctccagcgtcacctc	Protospacer
 * * ******.***** ************

34. spacer 8.2|4795878|26|NZ_CP022203|CRT matches to MN204493 (Streptomyces phage Zuko, complete genome) position: , mismatch: 6, identity: 0.769

atgatgatgccgccgtcctcttcacc	CRISPR spacer
ttgatgatgccgccgccctcttgctg	Protospacer
 **************.******  .

35. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP021367 (Acidovorax carolinensis strain P4 plasmid pACP4.1, complete sequence) position: , mismatch: 6, identity: 0.8

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
acgcccggggcgcccggacgctgcaaggtg	Protospacer
.***************** ** *** * .*

36. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP021363 (Acidovorax carolinensis strain P3 plasmid pACP3.1, complete sequence) position: , mismatch: 6, identity: 0.8

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
acgcccggggcgcccggacgctgcaaggtg	Protospacer
.***************** ** *** * .*

37. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 6, identity: 0.778

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
tagcgggcgcccagcggcgcggcgccg	Protospacer
 ..*********.*****.*******.

38. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NC_017966 (Tistrella mobilis KA081020-065 plasmid pTM2, complete sequence) position: , mismatch: 6, identity: 0.778

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
tggcgggcgcccggcggcgcggcgagg	Protospacer
 *.***************.*****  .

39. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NC_025024 (Burkholderia glumae strain BGR1 plasmid pBGA40, complete sequence) position: , mismatch: 6, identity: 0.778

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
caccaggcgcccggcggcgcggcgccg	Protospacer
 . *.*************.*******.

40. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 6, identity: 0.778

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
cttgtccgggtccgtgcccagcttgaa	Protospacer
 ****.**************** ..*

41. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 6, identity: 0.778

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
cttgtccgggtccgtgcccagcttgaa	Protospacer
 ****.**************** ..*

42. spacer 16.30|8645321|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP007130 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 2, complete sequence) position: , mismatch: 6, identity: 0.824

ggtgcgtcgtcctcgactgcgaggcggacgccgg	CRISPR spacer
agcgccgcgtcctcgacggcgaggcggccgccgg	Protospacer
.*.**  ********** ********* ******

43. spacer 16.45|8646397|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013109 (Sinorhizobium americanum strain CFNEI 73 plasmid B, complete sequence) position: , mismatch: 6, identity: 0.829

cgggcgcggcaggcggtggagacgctggtggtcga	CRISPR spacer
ctgccggcgccggcagtggagacgctggtggtcga	Protospacer
* * **  ** ***.********************

44. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 7, identity: 0.774

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
cgtacgtcgcccggcccggcaccgtcagccg	Protospacer
  * ************** ** ***** *.*

45. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 7, identity: 0.774

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
cgtacgtcgcccggcccggcaccgtcagccg	Protospacer
  * ************** ** ***** *.*

46. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NZ_CP038638 (Cupriavidus oxalaticus strain X32 plasmid unnamed3, complete sequence) position: , mismatch: 7, identity: 0.774

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
actccggcgccaggcccgccagcacggcatg	Protospacer
****** **** ***********.. .* **

47. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_AP022319 (Burkholderia sp. THE68 plasmid BTHE68_p1, complete sequence) position: , mismatch: 7, identity: 0.794

ccttgcgcg-cgtccacgccgcgcacggtgacgat	CRISPR spacer
-tcggcgcgtcgttcacgccgcgcacggtgatgac	Protospacer
 .. ***** ***.*****************.**.

48. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP013855 (Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence) position: , mismatch: 7, identity: 0.767

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
gcgcccggtgcgcccggaagcgggaccgct	Protospacer
******** *********.**** *.  *

49. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP007794 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p1, complete sequence) position: , mismatch: 7, identity: 0.767

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
ggggccgaggcgcccggaggcggcagctcc	Protospacer
* * ***.*****************  .*

50. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP054615 (Azospirillum oryzae strain KACC 14407 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.767

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
ggtgccgggacggccggaggcggcatggca	Protospacer
*   *****.** ************** *.

51. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP032322 (Azospirillum brasilense strain MTCC4035 plasmid p1, complete sequence) position: , mismatch: 7, identity: 0.767

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
ggggccgaggcgcccggaggcggcagctcc	Protospacer
* * ***.*****************  .*

52. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to KY092482 (Streptomyces phage Mojorita, complete genome) position: , mismatch: 7, identity: 0.767

acgcccggccccggcggaacccccggacgg	CRISPR spacer
tctcgacgccccggcggcaccgccggacgg	Protospacer
 * *   ********** *** ********

53. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to KY092480 (Streptomyces phage Picard, complete genome) position: , mismatch: 7, identity: 0.767

acgcccggccccggcggaacccccggacgg	CRISPR spacer
tctcgacgccccggcggcaccgccggacgg	Protospacer
 * *   ********** *** ********

54. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 7, identity: 0.741

ggacgggcgcccggcggcacggcgcca	CRISPR spacer
ccgcgggcgaccggcggcacggcggtg	Protospacer
  .****** ************** ..

55. spacer 12.1|6778349|30|NZ_CP022203|PILER-CR matches to NC_019789 (Deinococcus peraridilitoris DSM 19664 plasmid pDEIPE01, complete sequence) position: , mismatch: 7, identity: 0.767

atcgagcggatccgtccccccgacgttcac---	CRISPR spacer
ttcgagcggatccgtcccc---acgtgcgtggt	Protospacer
 ******************   **** *..

56. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to NZ_CP045122 (Rubrobacter sp. SCSIO 52915 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.741

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
cgcgtccgggtccgtgcccagcgcgcg	Protospacer
  .**.******************.

57. spacer 12.2|6778418|27|NZ_CP022203|PILER-CR matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 7, identity: 0.741

gttgttcgggtccgtgcccagcgcaat	CRISPR spacer
cgagttcgggtccgcgcccagcgcgtc	Protospacer
   ***********.*********. .

58. spacer 17.1|8648986|32|NZ_CP022203|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP010630 (Phaeobacter inhibens strain P78 plasmid pP78_a, complete sequence) position: , mismatch: 7, identity: 0.781

aggcgctacgcatcatcggcgcttccgggcag	CRISPR spacer
aacctatacgcatcatcggcgtttccggtcac	Protospacer
*. *  ***************.****** **

59. spacer 17.1|8648986|32|NZ_CP022203|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP050647 (Escherichia coli strain PapM-36-2 plasmid pIncFIB, complete sequence) position: , mismatch: 7, identity: 0.781

aggcgctacgcatcatcggcgcttccgggcag	CRISPR spacer
gggtggcgcgtatcaccggcgcttccgggcag	Protospacer
.**.* ..**.****.****************

60. spacer 17.1|8648986|32|NZ_CP022203|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP010126 (Escherichia coli strain C8 plasmid A, complete genome) position: , mismatch: 7, identity: 0.781

aggcgctacgcatcatcggcgcttccgggcag	CRISPR spacer
gggtggcgcgtatcaccggcgcttccgggcag	Protospacer
.**.* ..**.****.****************

61. spacer 17.1|8648986|32|NZ_CP022203|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP031323 (Escherichia coli strain ST2350 isolate Es_ST2350_SE1_NDM_03_2018 plasmid pEsST2350_SE_2, complete sequence) position: , mismatch: 7, identity: 0.781

aggcgctacgcatcatcggcgcttccgggcag	CRISPR spacer
gggtggcgcgtatcaccggcgcttccgggcag	Protospacer
.**.* ..**.****.****************

62. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NZ_CP041045 (Paracoccus sp. AK26 plasmid pAK1, complete sequence) position: , mismatch: 7, identity: 0.788

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
tggcgaaccacggcgaagccctcggcctcggcg	Protospacer
  **   ***** ** *****************

63. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NZ_CP044425 (Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence) position: , mismatch: 7, identity: 0.788

-gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
agcgtcat-gacgtcgtcgcccccggcctcggcg	Protospacer
 *.*.* *  ******* ****.***********

64. spacer 18.50|8682100|33|NZ_CP022203|PILER-CR matches to NZ_LR723678 (Arsenite-oxidising bacterium NT-25 plasmid 2) position: , mismatch: 7, identity: 0.788

tgggaggcgctacgcgggctggacgtc-cgtccg	CRISPR spacer
catgaggagctgcgcgggctggacgtcgcgacc-	Protospacer
.. **** ***.*************** ** **

65. spacer 18.50|8682100|33|NZ_CP022203|PILER-CR matches to NZ_FO082821 (Rhizobium sp. NT-26 plasmid NT26_p1, complete sequence) position: , mismatch: 7, identity: 0.788

tgggaggcgctacgcgggctggacgtc-cgtccg	CRISPR spacer
catgaggagctgcgcgggctggacgtcgcgacc-	Protospacer
.. **** ***.*************** ** **

66. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP041045 (Paracoccus sp. AK26 plasmid pAK1, complete sequence) position: , mismatch: 7, identity: 0.788

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
tggcgaaccacggcgaagccctcggcctcggcg	Protospacer
  **   ***** ** *****************

67. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP044425 (Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence) position: , mismatch: 7, identity: 0.788

-gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
agcgtcat-gacgtcgtcgcccccggcctcggcg	Protospacer
 *.*.* *  ******* ****.***********

68. spacer 18.100|8682097|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_LR723678 (Arsenite-oxidising bacterium NT-25 plasmid 2) position: , mismatch: 7, identity: 0.788

tgggaggcgctacgcgggctggacgtc-cgtccg	CRISPR spacer
catgaggagctgcgcgggctggacgtcgcgacc-	Protospacer
.. **** ***.*************** ** **

69. spacer 18.100|8682097|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_FO082821 (Rhizobium sp. NT-26 plasmid NT26_p1, complete sequence) position: , mismatch: 7, identity: 0.788

tgggaggcgctacgcgggctggacgtc-cgtccg	CRISPR spacer
catgaggagctgcgcgggctggacgtcgcgacc-	Protospacer
.. **** ***.*************** ** **

70. spacer 19.1|8817623|40|NZ_CP022203|CRISPRCasFinder matches to NZ_CP029831 (Azospirillum ramasamyi strain M2T2B2 plasmid unnamed7, complete sequence) position: , mismatch: 7, identity: 0.825

cccagccgcatgcgggcgcggcgcaagctccgtgcgcccc---	CRISPR spacer
cccagccccatgcgggcgcgccgcaagccgc---cgccccaca	Protospacer
******* ************ *******. *   ******

71. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 8, identity: 0.742

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
cgatcaccgcctggcccgccggcgtcacctg	Protospacer
   .*..****.********.**********

72. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NZ_CP023071 (Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence) position: , mismatch: 8, identity: 0.742

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
cgatcaccgcctggcccgccggcgtcacctg	Protospacer
   .*..****.********.**********

73. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NZ_CP029232 (Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence) position: , mismatch: 8, identity: 0.742

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
cgatcaccgcctggcccgccggcgtcacctg	Protospacer
   .*..****.********.**********

74. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NZ_CP031166 (Euzebya sp. DY32-46 plasmid pEDY32-46I, complete sequence) position: , mismatch: 8, identity: 0.742

actccgtcgcccggcccgccagcgtcacctg	CRISPR spacer
caccagtcgcccggcccgcccgcgccacgcg	Protospacer
  .* *************** ***.*** .*

75. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_LR134465 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 23, complete sequence) position: , mismatch: 8, identity: 0.765

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
ccttgcgcgcgttcacgccgcccacgacgttcgt	Protospacer
************.******** ****..* . .*

76. spacer 11.4|5516783|33|NZ_CP022203|CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 8, identity: 0.758

ggccccggcggacgcgcacccggcggcatccca----	CRISPR spacer
tcccccggcggacccgcagccggcgg----ccatggc	Protospacer
  *********** **** *******    ***

77. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NC_010578 (Beijerinckia indica subsp. indica ATCC 9039 plasmid pBIND02, complete sequence) position: , mismatch: 8, identity: 0.733

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
tttaccggggcgcgccgaggcggcatgatg	Protospacer
 .  ********* * *********** .*

78. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NZ_CP016083 (Streptomyces sp. SAT1 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
ctgcccggccccggcgggaccgccgcgctc	Protospacer
 .***************.*** *** .*

79. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
gcgcccggccctggcggaacccgaccacct	Protospacer
.**********.**********    **

80. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
ccccccggcaccggcggaatccccggcgcc	Protospacer
 * ****** *********.******

81. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
ccccccggcaccggcggaatccccggcgcc	Protospacer
 * ****** *********.******

82. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NZ_CP019484 (Sinorhizobium meliloti strain B401 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
gatttccgccccggcggaacagccggacgg	Protospacer
.  ..* *************  ********

83. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NZ_CP019487 (Sinorhizobium meliloti strain B399 plasmid pSym, complete sequence) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
gatttccgccccggcggaacagccggacgg	Protospacer
.  ..* *************  ********

84. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to MK967402 (Mycobacterium phage NihilNomen, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
cggaggggccgcggcggaaaccccggacgt	Protospacer
  *   **** ******** *********

85. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to MH727551 (Mycobacterium phage Kalah2, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
cggaggggccgcggcggaaaccccggacgt	Protospacer
  *   **** ******** *********

86. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to JN116822 (Rhodococcus phage RRH1, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
ggacccggccccggcggatccgccggccac	Protospacer
. .*************** ** **** *.

87. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NC_014458 (Mycobacterium phage Angelica, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
acgcccggccccgacggaacgcctgagatc	Protospacer
*************.****** **.*..

88. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to MG962364 (Mycobacterium phage Deby, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
acgcccggccccgacggaacgcctgagatc	Protospacer
*************.****** **.*..

89. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to MK524527 (Mycobacterium phage ThreeRngTarjay, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
cggaggggccgcggcggaaaccccggacgt	Protospacer
  *   **** ******** *********

90. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to MK524529 (Mycobacterium phage Phoebus, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
cggaggggccgcggcggaaaccccggacgt	Protospacer
  *   **** ******** *********

91. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to MF919532 (Mycobacterium phage Sulley, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
acgcccggccccgacggaacgcctgagatc	Protospacer
*************.****** **.*..

92. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to KF114875 (Mycobacterium phage Redno2, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
cggaggggccgcggcggaaaccccggacgt	Protospacer
  *   **** ******** *********

93. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to MK524504 (Mycobacterium phage Hughesyang, complete genome) position: , mismatch: 8, identity: 0.733

acgcccggccccggcggaacccccggacgg	CRISPR spacer
cggaggggccgcggcggaaaccccggacgt	Protospacer
  *   **** ******** *********

94. spacer 12.1|6778349|30|NZ_CP022203|PILER-CR matches to NC_010070 (Burkholderia multivorans ATCC 17616 plasmid pBMUL01, complete sequence) position: , mismatch: 8, identity: 0.733

atcgagcggatccgtccccccgacgttcac	CRISPR spacer
aaatagcgaatccgtgcccccgacgttact	Protospacer
*   ****.****** ***********  .

95. spacer 12.1|6778349|30|NZ_CP022203|PILER-CR matches to NC_010802 (Burkholderia multivorans ATCC 17616 plasmid pTGL1, complete sequence) position: , mismatch: 8, identity: 0.733

atcgagcggatccgtccccccgacgttcac	CRISPR spacer
aaatagcgaatccgtgcccccgacgttact	Protospacer
*   ****.****** ***********  .

96. spacer 16.27|8645110|34|NZ_CP022203|CRISPRCasFinder,CRT matches to MN034385 (Leviviridae sp. isolate H2_Rhizo_31_scaffold_518 hypothetical protein (H2Rhizo31518_000001) gene, partial cds; and hypothetical protein (H2Rhizo31518_000002), RNA-dependent RNA polymerase (H2Rhizo31518_000003), and hypothetical protein (H2Rhizo31518_000004) genes, complete cds) position: , mismatch: 8, identity: 0.765

catgg-agcctgaaccgccgctgggtcctctcggc--	CRISPR spacer
-ataacagcctgaaccgccgctggggc--gtcagccg	Protospacer
 **.. ******************* *   **.**

97. spacer 16.27|8645110|34|NZ_CP022203|CRISPRCasFinder,CRT matches to MN035339 (Leviviridae sp. isolate H2_Rhizo_33_scaffold_3580 sequence) position: , mismatch: 8, identity: 0.765

catgg-agcctgaaccgccgctgggtcctctcggc--	CRISPR spacer
-ataacagcctgaaccgccgctggggc--gtcagccg	Protospacer
 **.. ******************* *   **.**

98. spacer 16.27|8645110|34|NZ_CP022203|CRISPRCasFinder,CRT matches to MN035781 (Leviviridae sp. isolate H4_Bulk_47_scaffold_337 hypothetical protein (H4Bulk47337_000001) gene, partial cds; and hypothetical protein (H4Bulk47337_000002), RNA-dependent RNA polymerase (H4Bulk47337_000003), and hypothetical protein (H4Bulk47337_000004) genes, complete cds) position: , mismatch: 8, identity: 0.765

catgg-agcctgaaccgccgctgggtcctctcggc--	CRISPR spacer
-ataacagcctgaaccgccgctggggc--gtcagcca	Protospacer
 **.. ******************* *   **.**

99. spacer 16.46|8646468|33|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027859 (Streptomyces clavuligerus strain ATCC 27064 plasmid pCLA1, complete sequence) position: , mismatch: 8, identity: 0.758

cactggaggtgcccggtgagcgccccggtgaag	CRISPR spacer
cggcggaggaacccggtgagcgccccggcgggg	Protospacer
*. .***** .*****************.*..*

100. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to MK494123 (Mycobacterium phage Blackbeetle, complete genome) position: , mismatch: 8, identity: 0.765

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
cgcatcgcgcacgaggcggcatcggcgatcgcaa	Protospacer
***** ****.**************   *  **

101. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to MG757167 (Mycobacterium phage Tesla, complete genome) position: , mismatch: 8, identity: 0.765

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
cgcatcgcgcacgaggcggcatcggcgatcgcaa	Protospacer
***** ****.**************   *  **

102. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to MK305892 (Mycobacterium phage RedRaider77, complete genome) position: , mismatch: 8, identity: 0.765

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
cgcatcgcgcacgaggcggcatcggcgatcgcaa	Protospacer
***** ****.**************   *  **

103. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to KJ538721 (Mycobacterium phage MosMoris, complete genome) position: , mismatch: 8, identity: 0.765

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
cgcatcgcgcacgaggcggcatcggcgatcgcaa	Protospacer
***** ****.**************   *  **

104. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to MN329676 (Mycobacterium phage Poise, complete genome) position: , mismatch: 8, identity: 0.765

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
cgcatcgcgcacgaggcggcatcggcgatcgcaa	Protospacer
***** ****.**************   *  **

105. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to KX159477 (Mycobacterium phage Gattaca, complete genome) position: , mismatch: 8, identity: 0.765

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
cgcatcgcgcacgaggcggcatcggcgatcgcaa	Protospacer
***** ****.**************   *  **

106. spacer 17.1|8648986|32|NZ_CP022203|PILER-CR,CRISPRCasFinder,CRT matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 8, identity: 0.75

aggcgcta-cgcatcatcggcgcttccgggcag	CRISPR spacer
-accgtcaccgcatcctcggcgcgtccgggcaa	Protospacer
 . **..* ****** ******* ********.

107. spacer 18.25|8680307|35|NZ_CP022203|PILER-CR matches to NC_023722 (Rhodococcus phage ReqiPine5, complete genome) position: , mismatch: 8, identity: 0.771

tggcagaacccgacggtgacgaaggcggacgtgga	CRISPR spacer
gcgaacacctcggcggtgacgaaggcggccgtgga	Protospacer
  * * * *.**.*************** ******

108. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to JN106171 (Uncultured bacterium plasmid pAKD26, complete sequence) position: , mismatch: 8, identity: 0.765

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
ggctggtgaactccgggccgttgtcggtgcgcac	Protospacer
*** ****** ************** .. .***

109. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NZ_CP013369 (Burkholderia ubonensis strain RF23-BP41 plasmid pRF23, complete sequence) position: , mismatch: 8, identity: 0.765

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tgctgacgaactccgggccgttatccacctgaat	Protospacer
 ** *..*** ***********.******** *

110. spacer 18.30|8680665|33|NZ_CP022203|PILER-CR matches to NC_016817 (Pantoea ananatis LMG 5342 plasmid pPANA10, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

111. spacer 18.30|8680665|33|NZ_CP022203|PILER-CR matches to NZ_CP020944 (Pantoea ananatis strain PNA 97-1R plasmid unamed1, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

112. spacer 18.30|8680665|33|NZ_CP022203|PILER-CR matches to NC_017553 (Pantoea ananatis PA13 plasmid PAGR_p, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

113. spacer 18.30|8680665|33|NZ_CP022203|PILER-CR matches to NZ_CP022429 (Pantoea ananatis strain YJ76 plasmid p_unamed1) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

114. spacer 18.30|8680665|33|NZ_CP022203|PILER-CR matches to NC_017533 (Pantoea ananatis AJ13355 plasmid pEA320, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

115. spacer 18.30|8680665|33|NZ_CP022203|PILER-CR matches to NZ_CP014208 (Pantoea ananatis strain R100 plasmid, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

116. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH271319 (Rhodococcus UhSalsa, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

117. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MF324902 (Rhodococcus phage Krishelle, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

118. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to KT959213 (Rhodococcus phage TWAMP, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

119. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH271297 (Rhodococcus phage Erik, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

120. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH271309 (Rhodococcus phage Phrankenstein, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

121. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MF324904 (Rhodococcus phage RexFury, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

122. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MF324901 (Rhodococcus phage Naiad, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

123. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to KT990218 (Rhodococcus phage Lillie, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

124. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to KX550082 (Rhodococcus phage Natosaleda, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

125. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MK524495 (Rhodococcus phage Belenaria, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

126. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH271299 (Rhodococcus phage Gollum, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

127. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH271293 (Rhodococcus phage Bradshaw, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

128. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NC_028677 (Rhodococcus phage CosmicSans, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

129. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH271306 (Rhodococcus phage Nancinator, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

130. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH271314 (Rhodococcus phage Swann, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

131. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MF324900 (Rhodococcus phage StCroix, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

132. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH316569 (Rhodococcus phage Shuman, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

133. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to KT375356 (Rhodococcus phage Rhodalysa, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

134. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MK524487 (Rhodococcus phage Espica, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

135. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NC_016653 (Rhodococcus phage RER2, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

136. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MF324905 (Rhodococcus phage Alatin, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

137. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NZ_AP019795 (Thermus thermophilus strain AA2-29 plasmid pAA229, complete sequence) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
gcccagtccacggcgtggccctcggcctcgagg	Protospacer
*. *  ****** ***.*************. *

138. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 8, identity: 0.758

gtgccctc---cacgtcgtagccctcggcctcggcg	CRISPR spacer
---tccttgaacagggcgtagccctcggcctcggcc	Protospacer
   .***.   ** * *******************

139. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NZ_AP019793 (Thermus thermophilus strain AA2-20 plasmid pAA220, complete sequence) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
gcccagtccacggcgtggccctcggcctcgagg	Protospacer
*. *  ****** ***.*************. *

140. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to MH047631 (Microbacterium phage Triscuit, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
tcgagctcctcgtcgtcgccctcggcctcttcg	Protospacer
 .*  **** ****** ************  **

141. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_010158 (Yersinia pestis Angola plasmid pMT-pPCP, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

142. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_015382 (Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcgagctaagcg	CRISPR spacer
gttcaacgcatccgtactcgtcgcgctcaccc	Protospacer
* . *** *************** *** * *

143. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_005815 (Yersinia pestis biovar Microtus str. 91001 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

144. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009490 (Yersinia pestis strain PBM19 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

145. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009714 (Yersinia pestis Pestoides F plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

146. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009702 (Yersinia pestis strain Harbin35 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

147. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009784 (Yersinia pestis strain El Dorado plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

148. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009722 (Yersinia pestis strain Shasta plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

149. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP045259 (Yersinia pestis strain SCPM-O-B-5942 (I-2638) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

150. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_014022 (Yersinia pestis Z176003 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

151. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_017266 (Yersinia pestis biovar Medievalis str. Harbin 35 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

152. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP033694 (Yersinia pestis strain FDAARGOS_602 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

153. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_009378 (Yersinia pestis Pestoides F plasmid MT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

154. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP033700 (Yersinia pestis strain FDAARGOS_601 plasmid unnamed3) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

155. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP033700 (Yersinia pestis strain FDAARGOS_601 plasmid unnamed3) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

156. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_006323 (Yersinia pestis plasmid pG8786, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

157. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP045146 (Yersinia pestis strain SCPM-O-B-6899 (231) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

158. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP045164 (Yersinia pestis strain SCPM-O-B-6291 (C-25) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

159. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP045155 (Yersinia pestis strain SCPM-O-B-5935 (I-1996) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

160. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP045159 (Yersinia pestis subsp. pestis bv. Medievalis strain SCPM-O-B-6530 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

161. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP006746 (Yersinia pestis 8787 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

162. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_003134 (Yersinia pestis CO92 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

163. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP045150 (Yersinia pestis strain SCPM-O-DNA-18 (I-3113) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

164. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP006790 (Yersinia pestis 2944 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

165. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP006749 (Yersinia pestis 3770 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

166. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP006756 (Yersinia pestis 1522 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

167. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_017155 (Yersinia pestis D106004 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

168. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_017158 (Yersinia pestis D182038 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

169. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_004835 (Yersinia pestis strain KIM5 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

170. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_004838 (Yersinia pestis KIM10+ plasmid pMT-1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

171. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP033692 (Yersinia pestis strain FDAARGOS_603 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

172. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP033693 (Yersinia pestis strain FDAARGOS_603 plasmid unnamed4) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

173. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP033693 (Yersinia pestis strain FDAARGOS_603 plasmid unnamed4) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

174. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP006760 (Yersinia pestis 1413 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

175. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP006779 (Yersinia pestis 1412 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

176. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP006752 (Yersinia pestis 3067 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

177. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NC_008118 (Yersinia pestis Nepal516 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

178. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP016275 (Yersinia pestis strain Cadman plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

179. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP019709 (Yersinia pestis strain 195/P plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

180. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009904 (Yersinia pestis Antiqua plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

181. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009841 (Yersinia pestis A1122 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

182. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009989 (Yersinia pestis strain Nicholisk 41 plasmid 1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

183. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP009934 (Yersinia pestis Angola plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

184. spacer 18.47|8681889|32|NZ_CP022203|PILER-CR matches to NZ_CP010021 (Yersinia pestis str. Pestoides B plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

185. spacer 18.75|8680304|35|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_023722 (Rhodococcus phage ReqiPine5, complete genome) position: , mismatch: 8, identity: 0.771

tggcagaacccgacggtgacgaaggcggacgtgga	CRISPR spacer
gcgaacacctcggcggtgacgaaggcggccgtgga	Protospacer
  * * * *.**.*************** ******

186. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to JN106171 (Uncultured bacterium plasmid pAKD26, complete sequence) position: , mismatch: 8, identity: 0.765

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
ggctggtgaactccgggccgttgtcggtgcgcac	Protospacer
*** ****** ************** .. .***

187. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP013369 (Burkholderia ubonensis strain RF23-BP41 plasmid pRF23, complete sequence) position: , mismatch: 8, identity: 0.765

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tgctgacgaactccgggccgttatccacctgaat	Protospacer
 ** *..*** ***********.******** *

188. spacer 18.80|8680662|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_016817 (Pantoea ananatis LMG 5342 plasmid pPANA10, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

189. spacer 18.80|8680662|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP020944 (Pantoea ananatis strain PNA 97-1R plasmid unamed1, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

190. spacer 18.80|8680662|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_017553 (Pantoea ananatis PA13 plasmid PAGR_p, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

191. spacer 18.80|8680662|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP022429 (Pantoea ananatis strain YJ76 plasmid p_unamed1) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

192. spacer 18.80|8680662|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_017533 (Pantoea ananatis AJ13355 plasmid pEA320, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

193. spacer 18.80|8680662|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP014208 (Pantoea ananatis strain R100 plasmid, complete sequence) position: , mismatch: 8, identity: 0.758

tctccagcaggacacgcatggcgacatctgggg	CRISPR spacer
cggcgggcagtacacgcatggcgccatctgggc	Protospacer
.  * .**** ************ ********

194. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH271319 (Rhodococcus UhSalsa, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

195. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MF324902 (Rhodococcus phage Krishelle, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

196. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to KT959213 (Rhodococcus phage TWAMP, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

197. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH271297 (Rhodococcus phage Erik, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

198. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH271309 (Rhodococcus phage Phrankenstein, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

199. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MF324904 (Rhodococcus phage RexFury, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

200. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MF324901 (Rhodococcus phage Naiad, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

201. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to KT990218 (Rhodococcus phage Lillie, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

202. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to KX550082 (Rhodococcus phage Natosaleda, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

203. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MK524495 (Rhodococcus phage Belenaria, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

204. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH271299 (Rhodococcus phage Gollum, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

205. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH271293 (Rhodococcus phage Bradshaw, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

206. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_028677 (Rhodococcus phage CosmicSans, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

207. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH271306 (Rhodococcus phage Nancinator, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

208. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH271314 (Rhodococcus phage Swann, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

209. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MF324900 (Rhodococcus phage StCroix, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

210. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH316569 (Rhodococcus phage Shuman, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

211. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to KT375356 (Rhodococcus phage Rhodalysa, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

212. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MK524487 (Rhodococcus phage Espica, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

213. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_016653 (Rhodococcus phage RER2, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

214. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MF324905 (Rhodococcus phage Alatin, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
caaagctcctcgtcggagccctcggcctcggcc	Protospacer
  .  **** ***** ****************

215. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_AP019795 (Thermus thermophilus strain AA2-29 plasmid pAA229, complete sequence) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
gcccagtccacggcgtggccctcggcctcgagg	Protospacer
*. *  ****** ***.*************. *

216. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 8, identity: 0.758

gtgccctc---cacgtcgtagccctcggcctcggcg	CRISPR spacer
---tccttgaacagggcgtagccctcggcctcggcc	Protospacer
   .***.   ** * *******************

217. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_AP019793 (Thermus thermophilus strain AA2-20 plasmid pAA220, complete sequence) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
gcccagtccacggcgtggccctcggcctcgagg	Protospacer
*. *  ****** ***.*************. *

218. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MH047631 (Microbacterium phage Triscuit, complete genome) position: , mismatch: 8, identity: 0.758

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
tcgagctcctcgtcgtcgccctcggcctcttcg	Protospacer
 .*  **** ****** ************  **

219. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_010158 (Yersinia pestis Angola plasmid pMT-pPCP, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

220. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_015382 (Burkholderia gladioli BSR3 plasmid bgla_1p, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcgagctaagcg	CRISPR spacer
gttcaacgcatccgtactcgtcgcgctcaccc	Protospacer
* . *** *************** *** * *

221. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_005815 (Yersinia pestis biovar Microtus str. 91001 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

222. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009490 (Yersinia pestis strain PBM19 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

223. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009714 (Yersinia pestis Pestoides F plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

224. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009702 (Yersinia pestis strain Harbin35 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

225. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009784 (Yersinia pestis strain El Dorado plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

226. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009722 (Yersinia pestis strain Shasta plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

227. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP045259 (Yersinia pestis strain SCPM-O-B-5942 (I-2638) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

228. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_014022 (Yersinia pestis Z176003 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

229. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_017266 (Yersinia pestis biovar Medievalis str. Harbin 35 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

230. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP033694 (Yersinia pestis strain FDAARGOS_602 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

231. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_009378 (Yersinia pestis Pestoides F plasmid MT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

232. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP033700 (Yersinia pestis strain FDAARGOS_601 plasmid unnamed3) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

233. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP033700 (Yersinia pestis strain FDAARGOS_601 plasmid unnamed3) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

234. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_006323 (Yersinia pestis plasmid pG8786, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

235. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP045146 (Yersinia pestis strain SCPM-O-B-6899 (231) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

236. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP045164 (Yersinia pestis strain SCPM-O-B-6291 (C-25) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

237. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP045155 (Yersinia pestis strain SCPM-O-B-5935 (I-1996) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

238. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP045159 (Yersinia pestis subsp. pestis bv. Medievalis strain SCPM-O-B-6530 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

239. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP006746 (Yersinia pestis 8787 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

240. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_003134 (Yersinia pestis CO92 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

241. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP045150 (Yersinia pestis strain SCPM-O-DNA-18 (I-3113) plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

242. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP006790 (Yersinia pestis 2944 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

243. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP006749 (Yersinia pestis 3770 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

244. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP006756 (Yersinia pestis 1522 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

245. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_017155 (Yersinia pestis D106004 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

246. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_017158 (Yersinia pestis D182038 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

247. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_004835 (Yersinia pestis strain KIM5 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

248. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_004838 (Yersinia pestis KIM10+ plasmid pMT-1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

249. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP033692 (Yersinia pestis strain FDAARGOS_603 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

250. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP033693 (Yersinia pestis strain FDAARGOS_603 plasmid unnamed4) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

251. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP033693 (Yersinia pestis strain FDAARGOS_603 plasmid unnamed4) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

252. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP006760 (Yersinia pestis 1413 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

253. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP006779 (Yersinia pestis 1412 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

254. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP006752 (Yersinia pestis 3067 plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

255. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_008118 (Yersinia pestis Nepal516 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

256. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP016275 (Yersinia pestis strain Cadman plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

257. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP019709 (Yersinia pestis strain 195/P plasmid pMT1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

258. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009904 (Yersinia pestis Antiqua plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

259. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009841 (Yersinia pestis A1122 plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

260. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009989 (Yersinia pestis strain Nicholisk 41 plasmid 1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

261. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP009934 (Yersinia pestis Angola plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

262. spacer 18.97|8681886|32|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP010021 (Yersinia pestis str. Pestoides B plasmid pMT, complete sequence) position: , mismatch: 8, identity: 0.75

ggcaaacccatccgtactcgtcg--agctaagcg	CRISPR spacer
ggcaaacccttccgtagtcgtcggtggttcaa--	Protospacer
********* ****** ******  .*.* *.

263. spacer 1.2|31687|31|NZ_CP022203|CRT matches to NZ_CP020572 (Thermus aquaticus strain YT-1 plasmid p61, complete sequence) position: , mismatch: 9, identity: 0.71

actccgtc-------gcccggcccgccagcgtcacctg	CRISPR spacer
-------cggggaaggcccggcccgccagcaccacctg	Protospacer
       *       ***************..******

264. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP034087 (Methylocystis rosea strain GW6 plasmid pGW6_1, complete sequence) position: , mismatch: 9, identity: 0.735

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
ccatgcgcgcgtccgcgccgcgcagcccgagaac	Protospacer
** ***********.*********   .** .*.

265. spacer 11.4|5516783|33|NZ_CP022203|CRT matches to NZ_CP020041 (Streptomyces sp. 3211 isolate 3 plasmid p3211-2, complete sequence) position: , mismatch: 9, identity: 0.727

ggccccggcggacgcgcacccggcggcatccca	CRISPR spacer
ggcccaggcggacccgcacccggcactccaccg	Protospacer
***** ******* **********. . . **.

266. spacer 11.4|5516783|33|NZ_CP022203|CRT matches to NC_020894 (Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence) position: , mismatch: 9, identity: 0.727

ggccccggcggacgcgcacccggcggcatccca	CRISPR spacer
ggccccggccgacgcgcaaccggctgagcgcgc	Protospacer
********* ******** ***** * .. *

267. spacer 11.4|5516783|33|NZ_CP022203|CRT matches to NC_017766 (Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence) position: , mismatch: 9, identity: 0.727

ggccccggcggacgcgcacccggcggcatccca	CRISPR spacer
ggccccggccgacgcgcaaccggctgagcgcgc	Protospacer
********* ******** ***** * .. *

268. spacer 11.6|5516873|30|NZ_CP022203|CRT matches to NZ_CP037443 (Klebsiella sp. PO552 plasmid p2, complete sequence) position: , mismatch: 9, identity: 0.7

gcgcccggggcgcccggaggcggcatgccg	CRISPR spacer
gacgatggggcgcccggaggcgtcatggtt	Protospacer
*    .**************** **** .

269. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NZ_CP015867 (Streptomyces parvulus strain 2297 plasmid pSPA1, complete sequence) position: , mismatch: 9, identity: 0.7

acgcccggccccggcggaacccccggacgg	CRISPR spacer
cgccccggccccgccggaaccaccggcgaa	Protospacer
   ********** ******* ****  ..

270. spacer 11.8|5516990|30|NZ_CP022203|CRT matches to NZ_CP010990 (Pseudonocardia sp. EC080625-04 plasmid pFRP1-1, complete sequence) position: , mismatch: 9, identity: 0.7

acgcccggccccggcggaacccccggacgg	CRISPR spacer
ctccccggccccggcgggaccgccggggcc	Protospacer
 . **************.*** ****.

271. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_010070 (Burkholderia multivorans ATCC 17616 plasmid pBMUL01, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctgggggtggtg	CRISPR spacer
cctccgcaaccgtggcgtcgcgctgctgccgaat	Protospacer
******* ***.*************  * .*.

272. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP022369 (Azospirillum sp. TSH58 plasmid TSH58_p05, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctgggggtggtg	CRISPR spacer
cgctctgatccttggcggcgcgctgggggtggtg	Protospacer
* ..*    ** ***** ****************

273. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP013108 (Sinorhizobium americanum strain CFNEI 73 plasmid A, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctgggggtggtg	CRISPR spacer
cgaccgccatcatggcgtcgcgccggggagacgg	Protospacer
*  ******.*************.****. .  *

274. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP028965 (Burkholderia sp. IDO3 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctgggggtggtg	CRISPR spacer
cctccgcaaccttggcgtcgcgctgctgccgagt	Protospacer
******* *** *************  * .*.

275. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP028965 (Burkholderia sp. IDO3 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctgggggtggtg	CRISPR spacer
cctccgcaaccgtggcgtcgcgctgctgccgaat	Protospacer
******* ***.*************  * .*.

276. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_010802 (Burkholderia multivorans ATCC 17616 plasmid pTGL1, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctgggggtggtg	CRISPR spacer
cctccgcaaccgtggcgtcgcgctgctgccgaat	Protospacer
******* ***.*************  * .*.

277. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP023408 (Streptomyces fungicidicus strain TXX3120 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctgggggtggtg	CRISPR spacer
gttccgccgccatggcgtcgcgcagggcctccag	Protospacer
 .******.************** ***  *   *

278. spacer 16.13|8644114|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP023039 (Komagataeibacter saccharivorans strain CV1 plasmid unnamed3, complete sequence) position: , mismatch: 9, identity: 0.735

cctccgccaccatggcgtcgcgctggg-ggtggtg	CRISPR spacer
ggcccgcctccatggcctcgcgctgggcggccgc-	Protospacer
  .***** ******* ********** **. *.

279. spacer 16.20|8644612|35|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_021289 (Burkholderia insecticola plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.743

ggtaacacgctcctcgtcaacgagattttctacag	CRISPR spacer
gacgacacgcccttcgtcaacgagattttcagccc	Protospacer
*...******.*.***************** .*

280. spacer 16.20|8644612|35|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_AP022319 (Burkholderia sp. THE68 plasmid BTHE68_p1, complete sequence) position: , mismatch: 9, identity: 0.743

ggtaacacgctcctcgtcaacgagattttctacag	CRISPR spacer
gacgacacgcccttcgtcaacgagattttcagccc	Protospacer
*...******.*.***************** .*

281. spacer 16.31|8645391|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP049911 (Diaphorobacter sp. HDW4A plasmid p_unnamed1, complete sequence) position: , mismatch: 9, identity: 0.735

cgtggctgctgccgcagacgttcaacctcggcat	CRISPR spacer
gctggctgctgccgctcacgttcaaccgccacgc	Protospacer
  *************  ********** * .*..

282. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012748 (Paraburkholderia caribensis MBA4 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.757

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
cccggcagcgacgccgcgacctgctgcgcgagcgcgt	Protospacer
*.*..*  *..******* **.***************

283. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to MK511056 (Pseudomonas phage BR293, partial genome) position: , mismatch: 9, identity: 0.757

--ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
gggtcgcgtc--gcgccgcgtcccgtagcgcgagcgcga	Protospacer
   **.  **  *************. ***********

284. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to MK511055 (Pseudomonas phage BR204, partial genome) position: , mismatch: 9, identity: 0.757

--ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
gggtcgcgtc--gcgccgcgtcccgtagcgcgagcgcga	Protospacer
   **.  **  *************. ***********

285. spacer 16.50|8646749|33|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NC_013857 (Azospirillum sp. B510 plasmid pAB510c, complete sequence) position: , mismatch: 9, identity: 0.727

gaggctgaccgctacagcacccgggaggaagcc	CRISPR spacer
tctttcggcctctacaacacccgggaggaagcc	Protospacer
    ..*.** *****.****************

286. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP027025 (Streptomyces sp. WAC00288 plasmid p3, complete sequence) position: , mismatch: 9, identity: 0.735

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
agcatggcgcgccaggcggcatcggccgggacgg	Protospacer
 *********** ************ .  * *.

287. spacer 16.56|8647178|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 9, identity: 0.735

cgcatggcgcgcgaggcggcatcgggtctgtcac	CRISPR spacer
ggcaaggcgcgcgcggcggcatcggtggcggcgc	Protospacer
 *** ******** ***********   .* *.*

288. spacer 18.4|8678788|33|NZ_CP022203|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP013855 (Pseudonocardia sp. HH130630-07 plasmid pLS2-1, complete sequence) position: , mismatch: 9, identity: 0.727

cacgctgtcgaacgtcgccaacaccgtcaacac	CRISPR spacer
accgctgtcgagcgtcgccaactccggcgcttc	Protospacer
  *********.********** *** *. . *

289. spacer 18.4|8678788|33|NZ_CP022203|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP011869 (Pseudonocardia sp. HH130629-09 plasmid pLS1-1, complete sequence) position: , mismatch: 9, identity: 0.727

cacgctgtcgaacgtcgccaacaccgtcaacac	CRISPR spacer
accgctgtcgagcgtcgccaactccggcgcttc	Protospacer
  *********.********** *** *. . *

290. spacer 18.17|8679729|33|NZ_CP022203|PILER-CR matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
cgccaggtcctcccaggcgtcgtccagctcccc	Protospacer
.******* * **************..* .*

291. spacer 18.17|8679729|33|NZ_CP022203|PILER-CR matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
cgccaggtcctcccaggcgtcgtccagctcccc	Protospacer
.******* * **************..* .*

292. spacer 18.17|8679729|33|NZ_CP022203|PILER-CR matches to KY385381 (Mycobacterium phage EniyanLRS, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

293. spacer 18.17|8679729|33|NZ_CP022203|PILER-CR matches to MN585992 (Mycobacterium phage MaryV, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

294. spacer 18.17|8679729|33|NZ_CP022203|PILER-CR matches to NC_008206 (Mycobacteriophage Wildcat, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

295. spacer 18.17|8679729|33|NZ_CP022203|PILER-CR matches to KP027195 (Mycobacterium phage Cosmo, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

296. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NZ_LR594660 (Variovorax sp. PBL-H6 plasmid 2) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

297. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NZ_LR594667 (Variovorax sp. SRS16 plasmid 2) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

298. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NC_008760 (Polaromonas naphthalenivorans CJ2 plasmid pPNAP04, complete sequence) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
ggctggtgaactccgggccgttgtcagtgcgaac	Protospacer
*** ****** ************** .. .* *

299. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NC_016968 (Comamonas testosteroni plasmid pTB30, complete sequence) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

300. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NZ_LR594672 (Variovorax sp. PBL-E5 plasmid 2) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

301. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NC_019263 (Delftia acidovorans plasmid pLME1, complete sequence) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

302. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NC_008195 (Mycobacterium phage Cooper, complete genome) position: , mismatch: 9, identity: 0.727

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
atgcgctccacgtcgcagccctcggcgaagaac	Protospacer
.*** **********.**********   *.

303. spacer 18.33|8680885|33|NZ_CP022203|PILER-CR matches to NZ_LR134468 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 26, complete sequence) position: , mismatch: 9, identity: 0.727

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
agctcggcgacgacgtggccctcggcctcggcg	Protospacer
.  .*  * *** ***.****************

304. spacer 18.37|8681173|33|NZ_CP022203|PILER-CR matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 9, identity: 0.727

atcgaacgggcggagagcttgaccaccgcccgc	CRISPR spacer
ggcttcacggcggagaccttgaccaccgcgcgc	Protospacer
. *     ******** ************ ***

305. spacer 18.45|8681749|34|NZ_CP022203|PILER-CR matches to NZ_CP040821 (Paraoceanicella profunda strain D4M1 plasmid pD4M1C, complete sequence) position: , mismatch: 9, identity: 0.735

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
ccggcgcggtgcccggccccgccgcctaccgccg	Protospacer
. * * .* ** ** ******************

306. spacer 18.46|8681819|34|NZ_CP022203|PILER-CR matches to MN234221 (Arthrobacter phage Shepard, complete genome) position: , mismatch: 9, identity: 0.735

aagggcgcctgtctgacgctggtgggcctgctgc	CRISPR spacer
ttcgatgtctgtccgacgctggttggcctgctgt	Protospacer
   *..*.*****.********* *********.

307. spacer 18.52|8682241|36|NZ_CP022203|PILER-CR matches to KC661275 (Mycobacterium phage HINdeR, complete genome) position: , mismatch: 9, identity: 0.75

tcgctgggcgcgtggcgcgttcgactcgcg----ggtttc	CRISPR spacer
cggatggtcgcatggcgcgttcgactcgcgccacgg----	Protospacer
. * *** ***.******************    **

308. spacer 18.67|8679726|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
cgccaggtcctcccaggcgtcgtccagctcccc	Protospacer
.******* * **************..* .*

309. spacer 18.67|8679726|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
cgccaggtcctcccaggcgtcgtccagctcccc	Protospacer
.******* * **************..* .*

310. spacer 18.67|8679726|33|NZ_CP022203|CRISPRCasFinder,CRT matches to KY385381 (Mycobacterium phage EniyanLRS, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

311. spacer 18.67|8679726|33|NZ_CP022203|CRISPRCasFinder,CRT matches to MN585992 (Mycobacterium phage MaryV, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

312. spacer 18.67|8679726|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_008206 (Mycobacteriophage Wildcat, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

313. spacer 18.67|8679726|33|NZ_CP022203|CRISPRCasFinder,CRT matches to KP027195 (Mycobacterium phage Cosmo, complete genome) position: , mismatch: 9, identity: 0.727

tgccaggtacgcccaggcgtcgtccgacatcaa	CRISPR spacer
gacgggtcgcgcccaggcgttctccgacatcaa	Protospacer
 .* .* ..***********. ***********

314. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_LR594660 (Variovorax sp. PBL-H6 plasmid 2) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

315. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_LR594667 (Variovorax sp. SRS16 plasmid 2) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

316. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_008760 (Polaromonas naphthalenivorans CJ2 plasmid pPNAP04, complete sequence) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
ggctggtgaactccgggccgttgtcagtgcgaac	Protospacer
*** ****** ************** .. .* *

317. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_016968 (Comamonas testosteroni plasmid pTB30, complete sequence) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

318. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_LR594672 (Variovorax sp. PBL-E5 plasmid 2) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

319. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_019263 (Delftia acidovorans plasmid pLME1, complete sequence) position: , mismatch: 9, identity: 0.735

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
tggaggtgaactccgtgccgttgtccaccgtgat	Protospacer
 * .****** **** *************   *

320. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_008195 (Mycobacterium phage Cooper, complete genome) position: , mismatch: 9, identity: 0.727

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
atgcgctccacgtcgcagccctcggcgaagaac	Protospacer
.*** **********.**********   *.

321. spacer 18.83|8680882|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_LR134468 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 26, complete sequence) position: , mismatch: 9, identity: 0.727

gtgccctccacgtcgtagccctcggcctcggcg	CRISPR spacer
agctcggcgacgacgtggccctcggcctcggcg	Protospacer
.  .*  * *** ***.****************

322. spacer 18.87|8681170|33|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 9, identity: 0.727

atcgaacgggcggagagcttgaccaccgcccgc	CRISPR spacer
ggcttcacggcggagaccttgaccaccgcgcgc	Protospacer
. *     ******** ************ ***

323. spacer 18.95|8681746|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP040821 (Paraoceanicella profunda strain D4M1 plasmid pD4M1C, complete sequence) position: , mismatch: 9, identity: 0.735

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
ccggcgcggtgcccggccccgccgcctaccgccg	Protospacer
. * * .* ** ** ******************

324. spacer 18.96|8681816|34|NZ_CP022203|CRISPRCasFinder,CRT matches to MN234221 (Arthrobacter phage Shepard, complete genome) position: , mismatch: 9, identity: 0.735

aagggcgcctgtctgacgctggtgggcctgctgc	CRISPR spacer
ttcgatgtctgtccgacgctggttggcctgctgt	Protospacer
   *..*.*****.********* *********.

325. spacer 18.102|8682238|36|NZ_CP022203|CRISPRCasFinder,CRT matches to KC661275 (Mycobacterium phage HINdeR, complete genome) position: , mismatch: 9, identity: 0.75

tcgctgggcgcgtggcgcgttcgactcgcg----ggtttc	CRISPR spacer
cggatggtcgcatggcgcgttcgactcgcgccacgg----	Protospacer
. * *** ***.******************    **

326. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

327. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP021653 (Ralstonia solanacearum strain RS 488 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

328. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP021767 (Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

329. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP012940 (Ralstonia solanacearum strain UW163 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

330. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP012944 (Ralstonia solanacearum strain IBSBF1503 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

331. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP012688 (Ralstonia solanacearum strain UY031 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

332. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NC_017575 (Ralstonia solanacearum Po82 megaplasmid, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

333. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP026308 (Ralstonia solanacearum strain IBSBF 2571 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

334. spacer 1.3|31744|34|NZ_CP022203|CRT matches to CP047139 (Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

335. spacer 1.3|31744|34|NZ_CP022203|CRT matches to NZ_CP051295 (Ralstonia solanacearum strain CIAT_078 plasmid megaplasmid, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

336. spacer 1.3|31744|34|NZ_CP022203|CRT matches to CP047137 (Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence) position: , mismatch: 10, identity: 0.706

ccttgcgcgcgtccacgccgcgcacggtgacgat	CRISPR spacer
cgatgcgcacgtccacgccgcgcgcggccagcgc	Protospacer
*  *****.**************.***. *  ..

337. spacer 16.28|8645180|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP040722 (Rhodococcus pyridinivorans strain YF3 plasmid unnamed3, complete sequence) position: , mismatch: 10, identity: 0.714

ctggggcagggtgacctctacgaccgctacctggg	CRISPR spacer
gcccgcctcggtggcctctacgaccgctacgtggc	Protospacer
 .  * *  ****.**************** ***

338. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048224 (Aeromonas salmonicida subsp. salmonicida strain J223 plasmid pASal5, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

339. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP017144 (Aeromonas salmonicida subsp. masoucida strain RFAS1 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

340. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022171 (Aeromonas salmonicida strain S121 plasmid pS121-2, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

341. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022182 (Aeromonas salmonicida strain S68 plasmid pS68-1, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

342. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NC_009350 (Aeromonas salmonicida subsp. salmonicida A449 plasmid 5, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

343. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP038103 (Aeromonas salmonicida subsp. salmonicida strain SHY16-3432 plasmid pAsa5-3432, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

344. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP038104 (Aeromonas salmonicida subsp. salmonicida strain SHY16-3432 plasmid pAsa9-like, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

345. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP022177 (Aeromonas salmonicida strain S44 plasmid pS44-2, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

346. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_KY555070 (Aeromonas salmonicida subsp. salmonicida strain 01-B526 plasmid pAsa9, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

347. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_KY555069 (Aeromonas salmonicida subsp. salmonicida strain 01-B526 plasmid pAsa5, complete sequence) position: , mismatch: 10, identity: 0.714

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattgggcgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   ********** ************ **.

348. spacer 16.42|8646183|33|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to KY709687 (Salmonella phage 29485, complete genome) position: , mismatch: 10, identity: 0.697

gcttcaccacctcctcgtcctccgcccagggga	CRISPR spacer
atttcaccacctcctcttccgccgccaccatgt	Protospacer
..************** *** *****   . *

349. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP013104 (Paraburkholderia caribensis strain MWAP64 plasmid 1, complete sequence) position: , mismatch: 10, identity: 0.73

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
ccgggcagcgacgccgcgacctgctgcgcgagcgcgt	Protospacer
*. ..*  *..******* **.***************

350. spacer 16.45|8646397|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP045120 (Rubrobacter sp. SCSIO 52909 plasmid unnamed1, complete sequence) position: , mismatch: 10, identity: 0.714

cgggcgcggcaggcggtggagacgctggtggtcga	CRISPR spacer
ctcgaccggggggcggtggagacgctggtggggcg	Protospacer
*  *  *** .********************   .

351. spacer 16.45|8646397|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to KC292026 (Halovirus HGTV-1, complete genome) position: , mismatch: 10, identity: 0.714

cgggcgcggcaggcggtggagacgctggtggtcga	CRISPR spacer
agattggtcaaggcggtggtggcgctggtggtcga	Protospacer
 *. .*    ********* *.*************

352. spacer 18.28|8680522|34|NZ_CP022203|PILER-CR matches to NC_029005 (Streptomyces phage phiSAJS1, complete genome) position: , mismatch: 10, identity: 0.706

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
cgtcccagccgtccgggccgttgtcgaccagcag	Protospacer
 *.    *  *************** *** ****

353. spacer 18.43|8681606|37|NZ_CP022203|PILER-CR matches to NZ_CP010024 (Paraburkholderia fungorum strain ATCC BAA-463 plasmid pBIL, complete sequence) position: , mismatch: 10, identity: 0.73

agacttgcggcagcccggacaagtcgagcggctgccc	CRISPR spacer
gccctcgcggcaccccggacaagtcgagccgatcggc	Protospacer
.  **.****** **************** * *   *

354. spacer 18.54|8682383|34|NZ_CP022203|PILER-CR matches to NZ_KY349138 (Mycolicibacterium sp. CBMA 213 plasmid pCBMA213_2, complete sequence) position: , mismatch: 10, identity: 0.706

ggctacgctgggacgccgtgcgcgcccgctgggg	CRISPR spacer
acctgcgctgggacgccctgcgcgccgccggaca	Protospacer
. **.************ ********  * *. .

355. spacer 18.62|8682952|34|NZ_CP022203|PILER-CR matches to NZ_CP013739 (Streptomyces globisporus C-1027 plasmid SGLP1, complete sequence) position: , mismatch: 10, identity: 0.706

tgcctgcggcgcacggggcgtttgcggcggggag	CRISPR spacer
gctcccgggcgcccggggcgtttgcggcgcgggc	Protospacer
  .*.  ***** **************** **.

356. spacer 18.78|8680519|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_029005 (Streptomyces phage phiSAJS1, complete genome) position: , mismatch: 10, identity: 0.706

ggcgggtgaagtccgggccgttgtccacctgcag	CRISPR spacer
cgtcccagccgtccgggccgttgtcgaccagcag	Protospacer
 *.    *  *************** *** ****

357. spacer 18.93|8681603|37|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP010024 (Paraburkholderia fungorum strain ATCC BAA-463 plasmid pBIL, complete sequence) position: , mismatch: 10, identity: 0.73

agacttgcggcagcccggacaagtcgagcggctgccc	CRISPR spacer
gccctcgcggcaccccggacaagtcgagccgatcggc	Protospacer
.  **.****** **************** * *   *

358. spacer 18.104|8682380|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_KY349138 (Mycolicibacterium sp. CBMA 213 plasmid pCBMA213_2, complete sequence) position: , mismatch: 10, identity: 0.706

ggctacgctgggacgccgtgcgcgcccgctgggg	CRISPR spacer
acctgcgctgggacgccctgcgcgccgccggaca	Protospacer
. **.************ ********  * *. .

359. spacer 18.112|8682949|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP013739 (Streptomyces globisporus C-1027 plasmid SGLP1, complete sequence) position: , mismatch: 10, identity: 0.706

tgcctgcggcgcacggggcgtttgcggcggggag	CRISPR spacer
gctcccgggcgcccggggcgtttgcggcgcgggc	Protospacer
  .*.  ***** **************** **.

360. spacer 16.3|8643387|35|NZ_CP022203|CRISPRCasFinder,CRT matches to MG696115 (Plesiomonas phage phiP4-7, complete genome) position: , mismatch: 11, identity: 0.686

caagccgcgtcgttcgcgtggtgcttgttgaatag	CRISPR spacer
atggccgggtcgttcgcgtgctgcttgtagtgctc	Protospacer
  .**** ************ ******* * ..

361. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP048224 (Aeromonas salmonicida subsp. salmonicida strain J223 plasmid pASal5, complete sequence) position: , mismatch: 11, identity: 0.686

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattggacgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   .********* ************ **.

362. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NC_009350 (Aeromonas salmonicida subsp. salmonicida A449 plasmid 5, complete sequence) position: , mismatch: 11, identity: 0.686

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattggacgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   .********* ************ **.

363. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP038103 (Aeromonas salmonicida subsp. salmonicida strain SHY16-3432 plasmid pAsa5-3432, complete sequence) position: , mismatch: 11, identity: 0.686

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattggacgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   .********* ************ **.

364. spacer 16.40|8646034|35|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_KY555069 (Aeromonas salmonicida subsp. salmonicida strain 01-B526 plasmid pAsa5, complete sequence) position: , mismatch: 11, identity: 0.686

gtcccgctgcgcgagcgcgtcatcccgctcgtcag	CRISPR spacer
gcgattggacgcgagcgcctcatcccgctcgacaa	Protospacer
*.  .   .********* ************ **.

365. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021653 (Ralstonia solanacearum strain RS 488 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.703

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctacgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . * ********  ****************..

366. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP039340 (Ralstonia solanacearum strain UW386 plasmid pUW386, complete sequence) position: , mismatch: 11, identity: 0.703

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctacgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . * ********  ****************..

367. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP012688 (Ralstonia solanacearum strain UY031 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.703

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctacgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . * ********  ****************..

368. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to CP047139 (Ralstonia solanacearum strain CFBP 8695 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.703

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctacgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . * ********  ****************..

369. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to CP047137 (Ralstonia solanacearum strain CFBP 8697 plasmid unnamed, complete sequence) position: , mismatch: 11, identity: 0.703

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctacgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . * ********  ****************..

370. spacer 18.45|8681749|34|NZ_CP022203|PILER-CR matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 11, identity: 0.676

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
tggccctgtggatccgccccgccggacgtgaagt	Protospacer
********* **.***********  ... .  *

371. spacer 18.45|8681749|34|NZ_CP022203|PILER-CR matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 11, identity: 0.676

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
tggccctgtggatccgccccgccggacgtgaagt	Protospacer
********* **.***********  ... .  *

372. spacer 18.45|8681749|34|NZ_CP022203|PILER-CR matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 11, identity: 0.676

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
tggccctgtggatccgccccgccggacgtgaagt	Protospacer
********* **.***********  ... .  *

373. spacer 18.53|8682313|34|NZ_CP022203|PILER-CR matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 11, identity: 0.676

tggtaggcgcgtcgccggttgaggcgctgatgtc	CRISPR spacer
gcatcggcgcgtcgacggttgcggcgctggccgt	Protospacer
  .* ********* ****** *******..  .

374. spacer 18.53|8682313|34|NZ_CP022203|PILER-CR matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 11, identity: 0.676

tggtaggcgcgtcgccggttgaggcgctgatgtc	CRISPR spacer
gcatcggcgcgtcgacggttgcggcgctggccgt	Protospacer
  .* ********* ****** *******..  .

375. spacer 18.95|8681746|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 11, identity: 0.676

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
tggccctgtggatccgccccgccggacgtgaagt	Protospacer
********* **.***********  ... .  *

376. spacer 18.95|8681746|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 11, identity: 0.676

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
tggccctgtggatccgccccgccggacgtgaagt	Protospacer
********* **.***********  ... .  *

377. spacer 18.95|8681746|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP030772 (Streptomyces sp. YIM 121038 plasmid pSSP121038, complete sequence) position: , mismatch: 11, identity: 0.676

tggccctgttgacccgccccgccgcctaccgcct	CRISPR spacer
tggccctgtggatccgccccgccggacgtgaagt	Protospacer
********* **.***********  ... .  *

378. spacer 18.103|8682310|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 11, identity: 0.676

tggtaggcgcgtcgccggttgaggcgctgatgtc	CRISPR spacer
gcatcggcgcgtcgacggttgcggcgctggccgt	Protospacer
  .* ********* ****** *******..  .

379. spacer 18.103|8682310|34|NZ_CP022203|CRISPRCasFinder,CRT matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 11, identity: 0.676

tggtaggcgcgtcgccggttgaggcgctgatgtc	CRISPR spacer
gcatcggcgcgtcgacggttgcggcgctggccgt	Protospacer
  .* ********* ****** *******..  .

380. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP026091 (Ralstonia solanacearum strain IBSBF 2570 plasmid unnamed, complete sequence) position: , mismatch: 12, identity: 0.676

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctatgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . . ********  ****************..

381. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NC_014309 (Ralstonia solanacearum CFBP2957 plasmid RCFBPv3_mp, complete genome) position: , mismatch: 12, identity: 0.676

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctatgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . . ********  ****************..

382. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP026093 (Ralstonia solanacearum strain SFC plasmid unnamed, complete sequence) position: , mismatch: 12, identity: 0.676

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctatgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . . ********  ****************..

383. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021767 (Ralstonia solanacearum strain RS 489 plasmid unnamed, complete sequence) position: , mismatch: 12, identity: 0.676

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctatgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . . ********  ****************..

384. spacer 16.44|8646324|37|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP021765 (Ralstonia pseudosolanacearum strain CRMRs218 plasmid unnamed, complete sequence) position: , mismatch: 12, identity: 0.676

ctcaactccagcgccgcgtcccgctgcgcgagcgcgt	CRISPR spacer
accgctatgagcgccgccgcccgctgcgcgagcgcac	Protospacer
 .*. . . ********  ****************..

385. spacer 16.47|8646537|34|NZ_CP022203|CRISPRCasFinder,CRT,PILER-CR matches to NZ_CP018573 (Marivivens sp. JLT3646 plasmid unnamed, complete sequence) position: , mismatch: 12, identity: 0.647

tgagaggggtagagcgtgatttccatgacgtcat	CRISPR spacer
atttgcatgtagagcgtgagttcaatgacgtccg	Protospacer
    . . *********** *** ********

386. spacer 11.9|5517038|27|NZ_CP022203|CRT matches to NC_011887 (Methylobacterium nodulans ORS 2060 plasmid pMNOD02, complete sequence) position: , mismatch: 14, identity: 0.481

-----------ggacgggcgcccggcggcacggcgcca	CRISPR spacer
cggcgccgtcccgccaggcgcccggcg-----------	Protospacer
            * *.***********

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

1748000 : 1877447

119

Bacillus_phage(15.0%)

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

attL 1849835:1849854|attR 1864385:1864404

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_013935390.1\|1748000_1748288_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatC	NA	NA	NA	NA
WP_095957550.1\|1748306_1749767_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatA	NA	NA	NA	NA
WP_095957551.1\|1749799_1751239_+\|tRNA	Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase subunit GatB	NA	NA	NA	NA
WP_095957552.1\|1751235_1752291_-	carbon-nitrogen hydrolase family protein	NA	NA	NA	NA
WP_095957553.1\|1752297_1753260_-	isopenicillin N synthase family oxygenase	NA	NA	NA	NA
WP_095957554.1\|1753566_1755504_+	protein kinase	A0A2H4UVE2	Bodo_saltans_virus	2.3e-19	26.4
WP_095957555.1\|1755561_1755930_-	hypothetical protein	NA	NA	NA	NA
WP_013935383.1\|1756186_1756495_+	50S ribosomal protein L21	NA	NA	NA	NA
WP_043708982.1\|1756534_1756810_+	50S ribosomal protein L27	NA	NA	NA	NA
WP_095957556.1\|1758941_1759619_+	RNA methyltransferase	NA	NA	NA	NA
WP_095957557.1\|1759693_1760428_+	outer membrane lipoprotein carrier protein LolA	NA	NA	NA	NA
WP_095957558.1\|1760429_1761863_+	hypothetical protein	NA	NA	NA	NA
WP_095957559.1\|1761885_1762875_+	hypothetical protein	NA	NA	NA	NA
WP_013935376.1\|1762908_1764339_-	30S ribosomal protein S12 methylthiotransferase RimO	NA	NA	NA	NA
WP_043708979.1\|1764344_1765460_-	hypothetical protein	NA	NA	NA	NA
WP_013935374.1\|1765456_1765954_-	YajQ family cyclic di-GMP-binding protein	NA	NA	NA	NA
WP_095957560.1\|1765975_1767616_-	ribonuclease J	NA	NA	NA	NA
WP_157757458.1\|1767686_1771142_-	tetratricopeptide repeat protein	A0A2R3ZRI5	Marseillevirus	2.7e-10	25.6
WP_095957561.1\|1771288_1772191_+	acyl dehydratase	NA	NA	NA	NA
WP_095957562.1\|1772204_1773401_-	polysaccharide deacetylase family protein	NA	NA	NA	NA
WP_043708973.1\|1773633_1774206_+	hypothetical protein	NA	NA	NA	NA
WP_095957563.1\|1774221_1777044_-	AAA family ATPase	A0A223W0B1	Agrobacterium_phage	4.5e-48	26.5
WP_095957564.1\|1777386_1777929_-	HNH endonuclease	A0A1P8DIY8	Virus_Rctr197k	1.8e-46	50.8
WP_123784020.1\|1780038_1780419_+	hypothetical protein	NA	NA	NA	NA
WP_095961506.1\|1780723_1781929_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_157757459.1\|1782731_1783760_+	hypothetical protein	NA	NA	NA	NA
WP_095957566.1\|1784049_1785174_+	HNH endonuclease	NA	NA	NA	NA
WP_157757460.1\|1785270_1786182_-	hypothetical protein	NA	NA	NA	NA
WP_157757461.1\|1786587_1786725_+	hypothetical protein	NA	NA	NA	NA
WP_095957568.1\|1786984_1787647_+	class I SAM-dependent methyltransferase	NA	NA	NA	NA
WP_095957569.1\|1788262_1789842_-\|transposase	IS3 family transposase	A0A2P1JR32	Mycobacterium_phage	3.6e-10	28.4
WP_157757462.1\|1789887_1790208_-	hypothetical protein	NA	NA	NA	NA
WP_157757463.1\|1790260_1790449_+	hypothetical protein	NA	NA	NA	NA
WP_095957570.1\|1790764_1791067_+	hypothetical protein	NA	NA	NA	NA
WP_157757464.1\|1791314_1791743_+	hypothetical protein	NA	NA	NA	NA
WP_095961507.1\|1791958_1793740_-	DUF4209 domain-containing protein	NA	NA	NA	NA
WP_095961458.1\|1793908_1795057_-\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_157757465.1\|1795312_1796440_+	hypothetical protein	A0A0A7RU01	Clostridium_phage	4.3e-18	36.7
WP_157757466.1\|1797056_1797254_-	hypothetical protein	NA	NA	NA	NA
WP_095961508.1\|1797773_1798379_+	RDD family protein	NA	NA	NA	NA
WP_095957573.1\|1798439_1800311_+	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_095961509.1\|1800364_1800796_-	cell wall protein	NA	NA	NA	NA
WP_095961510.1\|1801722_1801953_-	hypothetical protein	NA	NA	NA	NA
WP_095957574.1\|1801961_1802348_-	gamma-glutamylcyclotransferase	H9D1E0	Salinivibrio_phage	1.5e-10	36.4
WP_095957575.1\|1802344_1802785_-	gamma-glutamylcyclotransferase	NA	NA	NA	NA
WP_095957576.1\|1803321_1804740_+\|transposase	ISKra4 family transposase	NA	NA	NA	NA
WP_095957577.1\|1804856_1805822_-	amidoligase family protein	A0A1B1IUD7	uncultured_Mediterranean_phage	6.7e-76	50.0
WP_095957578.1\|1806227_1806566_-	hypothetical protein	NA	NA	NA	NA
WP_095957579.1\|1806788_1806974_-	hypothetical protein	NA	NA	NA	NA
WP_095957580.1\|1807095_1807458_-	hypothetical protein	NA	NA	NA	NA
WP_095957581.1\|1807466_1808084_-	DUF2924 domain-containing protein	NA	NA	NA	NA
WP_095957582.1\|1808198_1808423_-	hypothetical protein	NA	NA	NA	NA
WP_095957583.1\|1808935_1809373_-	hypothetical protein	NA	NA	NA	NA
WP_095957584.1\|1809381_1811292_-	hypothetical protein	NA	NA	NA	NA
WP_157757467.1\|1812194_1813457_+	hypothetical protein	NA	NA	NA	NA
WP_170114805.1\|1813638_1814574_-\|tail	phage tail protein	NA	NA	NA	NA
WP_082207158.1\|1814853_1815189_+	hypothetical protein	NA	NA	NA	NA
WP_013938504.1\|1815185_1815527_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_095961512.1\|1815604_1817302_+\|transposase	IS66 family transposase	A0A0P0ZEB3	Stx2-converting_phage	1.8e-39	29.3
WP_095957586.1\|1817574_1817970_-	hypothetical protein	NA	NA	NA	NA
WP_095957587.1\|1817974_1818670_-	hypothetical protein	NA	NA	NA	NA
WP_095957588.1\|1818677_1819208_-	hypothetical protein	NA	NA	NA	NA
WP_095961513.1\|1819209_1820721_-\|plate	baseplate J/gp47 family protein	NA	NA	NA	NA
WP_157757468.1\|1821627_1822119_+	hypothetical protein	NA	NA	NA	NA
WP_095957589.1\|1822174_1822561_-	hypothetical protein	NA	NA	NA	NA
WP_095957590.1\|1822568_1823240_-	hypothetical protein	NA	NA	NA	NA
WP_095957591.1\|1823248_1823827_-	hypothetical protein	NA	NA	NA	NA
WP_095957592.1\|1823837_1825121_-	phage late control D family protein	NA	NA	NA	NA
WP_095957593.1\|1825117_1825459_-	hypothetical protein	NA	NA	NA	NA
WP_095957594.1\|1825458_1825971_-	peptidoglycan-binding protein	NA	NA	NA	NA
WP_095957595.1\|1825986_1828680_-\|tail	phage tail tape measure protein	A0A2H4J055	uncultured_Caudovirales_phage	2.3e-17	23.3
WP_046711595.1\|1828683_1828875_-	hypothetical protein	NA	NA	NA	NA
WP_095957596.1\|1828871_1829645_-	hypothetical protein	NA	NA	NA	NA
WP_095957597.1\|1830206_1830668_-\|tail	phage tail protein	NA	NA	NA	NA
WP_095961514.1\|1830679_1831489_-\|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	3.3e-20	30.5
WP_095957598.1\|1832893_1833223_-	hypothetical protein	NA	NA	NA	NA
WP_095957599.1\|1833219_1834122_-	transcription factor	NA	NA	NA	NA
WP_095957600.1\|1834121_1834727_-	hypothetical protein	NA	NA	NA	NA
WP_095957601.1\|1834734_1835376_-	hypothetical protein	NA	NA	NA	NA
WP_095957602.1\|1835372_1835651_-	hypothetical protein	NA	NA	NA	NA
WP_095957603.1\|1835647_1836172_-	hypothetical protein	NA	NA	NA	NA
WP_095957604.1\|1836171_1836810_-	hypothetical protein	NA	NA	NA	NA
WP_013375346.1\|1836811_1837189_-	hypothetical protein	NA	NA	NA	NA
WP_095957605.1\|1837280_1838141_-\|capsid	phage major capsid protein	A0A1B1P7E3	Bacillus_phage	8.7e-35	42.3
WP_095957606.1\|1838187_1838877_-	hypothetical protein	NA	NA	NA	NA
WP_095957607.1\|1838873_1840226_-	DNA adenine methylase	A0A1B1P7E4	Bacillus_phage	4.4e-17	39.3
WP_002618804.1\|1840218_1840404_-	hypothetical protein	NA	NA	NA	NA
WP_095957608.1\|1840458_1841538_-\|head	head morphogenesis protein	NA	NA	NA	NA
WP_095957609.1\|1841518_1841800_-	hypothetical protein	NA	NA	NA	NA
WP_095957610.1\|1841796_1843821_-\|portal	phage portal protein	A0A0U3E050	Pseudomonas_phage	8.3e-52	30.8
WP_095957611.1\|1844037_1844925_+	hypothetical protein	NA	NA	NA	NA
WP_157757469.1\|1845184_1845976_+	hypothetical protein	NA	NA	NA	NA
WP_095957613.1\|1845972_1847178_+	ImmA/IrrE family metallo-endopeptidase	NA	NA	NA	NA
WP_157757470.1\|1847367_1848465_+	DUF3800 domain-containing protein	NA	NA	NA	NA
WP_095957615.1\|1848915_1850223_+\|transposase	IS21 family transposase	U5N3F9	Enterobacteria_phage	1.2e-27	31.5
1849835:1849854	attL	NA	NA	NA	NA
WP_095957616.1\|1850219_1851014_+	ATP-binding protein	U5N3V8	Enterobacteria_phage	2.6e-62	50.6
WP_095957617.1\|1851795_1852446_+	hypothetical protein	NA	NA	NA	NA
WP_095957618.1\|1852500_1852830_-	hypothetical protein	NA	NA	NA	NA
WP_013375354.1\|1853023_1853347_-\|terminase	phage terminase ATPase subunit	NA	NA	NA	NA
WP_095957619.1\|1853363_1854458_-\|terminase	terminase	NA	NA	NA	NA
WP_095957620.1\|1854538_1855153_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
WP_095957621.1\|1856203_1857175_-	AT hook motif domain protein	NA	NA	NA	NA
WP_095957622.1\|1857183_1858014_-	hypothetical protein	NA	NA	NA	NA
WP_095957623.1\|1857989_1858328_-	hypothetical protein	NA	NA	NA	NA
WP_095957624.1\|1858324_1858984_-	3'-5' exonuclease	A0A0A8WJ41	Clostridium_phage	5.9e-07	28.6
WP_095957625.1\|1858984_1860160_-	PD-(D/E)XK nuclease family protein	NA	NA	NA	NA
WP_095957626.1\|1860290_1860902_-	hypothetical protein	NA	NA	NA	NA
WP_013935609.1\|1862954_1863737_-	ATP-binding protein	U5N3V8	Enterobacteria_phage	9.3e-44	40.2
WP_095957627.1\|1863790_1865359_-\|transposase	IS21 family transposase	NA	NA	NA	NA
1864385:1864404	attR	NA	NA	NA	NA
WP_095957628.1\|1866139_1866481_+	hypothetical protein	NA	NA	NA	NA
WP_095961515.1\|1866486_1867224_+	hypothetical protein	NA	NA	NA	NA
WP_095957629.1\|1867311_1868829_+	DEAD/DEAH box helicase	A7WKN6	Acidianus_filamentous_virus	4.6e-23	27.6
WP_095957630.1\|1868855_1872065_+	hypothetical protein	NA	NA	NA	NA
WP_170114710.1\|1872235_1872409_+	hypothetical protein	NA	NA	NA	NA
WP_095957631.1\|1872500_1873079_+	DUF2924 domain-containing protein	K4I3X1	Acidithiobacillus_phage	2.1e-08	28.3
WP_095957632.1\|1873075_1873276_+	hypothetical protein	NA	NA	NA	NA
WP_095957634.1\|1874953_1875376_+	hypothetical protein	NA	NA	NA	NA
WP_095957635.1\|1875492_1876026_+	PspA	NA	NA	NA	NA
WP_095961516.1\|1876082_1877447_-\|transposase	IS701 family transposase	NA	NA	NA	NA

DBSCAN-SWA_2

2203365 : 2278681

Bacillus_phage(30.77%)

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

attL 2257700:2257715|attR 2286953:2286968

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_095957821.1\|2203365_2203893_+\|transposase	transposase	NA	NA	NA	NA
WP_095957822.1\|2204182_2205238_+	virulence RhuM family protein	Q9JMN3	Wolbachia_phage	6.0e-78	47.5
WP_095957823.1\|2206289_2206655_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_095957824.1\|2206671_2207790_+	ACR3 family arsenite efflux transporter	NA	NA	NA	NA
WP_095957825.1\|2207786_2208188_+	arsenate reductase ArsC	NA	NA	NA	NA
WP_095961542.1\|2208184_2208631_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_157757480.1\|2208657_2208942_-	metalloregulator ArsR/SmtB family transcription factor	NA	NA	NA	NA
WP_095957827.1\|2209016_2209589_-	hypothetical protein	NA	NA	NA	NA
WP_095957828.1\|2210338_2210755_-	hypothetical protein	NA	NA	NA	NA
WP_095957829.1\|2210783_2211386_-	c-type cytochrome	NA	NA	NA	NA
WP_095957830.1\|2211422_2213891_-	heavy metal translocating P-type ATPase	A0A218MNH6	uncultured_virus	2.7e-81	35.2
WP_095961543.1\|2214453_2215038_-	DUF305 domain-containing protein	NA	NA	NA	NA
WP_095957831.1\|2215256_2216291_-	hypothetical protein	NA	NA	NA	NA
WP_095957832.1\|2216446_2217847_-	sigma-54-dependent Fis family transcriptional regulator	NA	NA	NA	NA
WP_095961544.1\|2217843_2219271_-	HAMP domain-containing sensor histidine kinase	Q8QKV7	Ectocarpus_siliculosus_virus	7.2e-10	25.3
WP_095957833.1\|2219486_2220929_-	multicopper oxidase family protein	NA	NA	NA	NA
WP_095957834.1\|2221043_2224346_-	efflux RND transporter permease subunit	NA	NA	NA	NA
WP_095957835.1\|2224351_2225782_-	efflux RND transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_095957836.1\|2225795_2227280_-	TolC family protein	NA	NA	NA	NA
WP_095957837.1\|2227688_2228138_-	cupredoxin domain-containing protein	NA	NA	NA	NA
WP_095957839.1\|2229009_2230518_+	TolC family protein	NA	NA	NA	NA
WP_095957840.1\|2230630_2232001_+	copper oxidase	NA	NA	NA	NA
WP_095957841.1\|2232481_2232856_+	hypothetical protein	NA	NA	NA	NA
WP_095961545.1\|2232901_2233132_-	hypothetical protein	NA	NA	NA	NA
WP_095957842.1\|2233137_2233527_-	gamma-glutamylcyclotransferase	H9D1E0	Salinivibrio_phage	1.1e-10	36.4
WP_095957843.1\|2233523_2233964_-	gamma-glutamylcyclotransferase	NA	NA	NA	NA
WP_095957844.1\|2234097_2234301_-	hypothetical protein	NA	NA	NA	NA
WP_095957845.1\|2234496_2235462_-	amidoligase family protein	A0A1B1IUD7	uncultured_Mediterranean_phage	3.9e-76	50.7
WP_095957846.1\|2235838_2236120_-	hypothetical protein	NA	NA	NA	NA
WP_095957847.1\|2236299_2236545_-	hypothetical protein	NA	NA	NA	NA
WP_095957848.1\|2236624_2236966_-	hypothetical protein	NA	NA	NA	NA
WP_095957849.1\|2237164_2237503_-	hypothetical protein	NA	NA	NA	NA
WP_095957850.1\|2237681_2238104_-	hypothetical protein	NA	NA	NA	NA
WP_095957851.1\|2238174_2238810_-	hypothetical protein	NA	NA	NA	NA
WP_095957852.1\|2239178_2239541_-	hypothetical protein	NA	NA	NA	NA
WP_095957853.1\|2239545_2240166_-	DUF2924 domain-containing protein	NA	NA	NA	NA
WP_095957854.1\|2240279_2240504_-	hypothetical protein	NA	NA	NA	NA
WP_095957855.1\|2240576_2240873_-	hypothetical protein	NA	NA	NA	NA
WP_095957856.1\|2241017_2241455_-	hypothetical protein	NA	NA	NA	NA
WP_095957857.1\|2241466_2243377_-	hypothetical protein	NA	NA	NA	NA
WP_095957858.1\|2243441_2244779_-\|tail	phage tail protein	NA	NA	NA	NA
WP_095957859.1\|2244789_2245185_-	hypothetical protein	NA	NA	NA	NA
WP_095957860.1\|2245189_2245885_-	hypothetical protein	NA	NA	NA	NA
WP_095957861.1\|2245892_2246423_-	hypothetical protein	NA	NA	NA	NA
WP_095961546.1\|2246424_2247936_-\|plate	baseplate J/gp47 family protein	NA	NA	NA	NA
WP_095957862.1\|2248031_2249393_-\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_141619463.1\|2249522_2250698_-	hypothetical protein	NA	NA	NA	NA
WP_095957863.1\|2250858_2251239_-	hypothetical protein	NA	NA	NA	NA
WP_095957864.1\|2251249_2251924_-	hypothetical protein	NA	NA	NA	NA
WP_095957865.1\|2251932_2252511_-	hypothetical protein	NA	NA	NA	NA
WP_095957866.1\|2252521_2253805_-	phage late control D family protein	NA	NA	NA	NA
WP_095957867.1\|2253801_2254143_-	hypothetical protein	NA	NA	NA	NA
WP_095957868.1\|2254142_2254655_-	peptidoglycan-binding protein	NA	NA	NA	NA
WP_095957869.1\|2254669_2257363_-\|tail	phage tail tape measure protein	A0A2H4J055	uncultured_Caudovirales_phage	2.2e-23	29.8
WP_095957870.1\|2257366_2257558_-	hypothetical protein	NA	NA	NA	NA
WP_095957871.1\|2257554_2258328_-	hypothetical protein	A0A127AX46	Bacillus_phage	3.4e-14	26.6
2257700:2257715	attL	NA	NA	NA	NA
WP_141619464.1\|2258386_2259100_-	MerC family mercury resistance protein	NA	NA	NA	NA
WP_095961547.1\|2259086_2259518_-	MerR family transcriptional regulator	NA	NA	NA	NA
WP_095957872.1\|2259596_2260058_-\|tail	phage tail protein	NA	NA	NA	NA
WP_157757481.1\|2260032_2260710_-	HNH endonuclease	M1U3A7	Cyanophage	2.5e-05	49.0
WP_170114723.1\|2260805_2261666_-\|tail	phage tail sheath family protein	J9PVC2	Bacillus_phage	3.8e-22	30.9
WP_095957876.1\|2263010_2263340_-	hypothetical protein	NA	NA	NA	NA
WP_095957877.1\|2263336_2264239_-	IPT/TIG domain-containing protein	NA	NA	NA	NA
WP_095957878.1\|2264238_2264844_-	hypothetical protein	NA	NA	NA	NA
WP_095957879.1\|2264851_2265493_-	hypothetical protein	NA	NA	NA	NA
WP_095957880.1\|2265489_2265798_-	hypothetical protein	NA	NA	NA	NA
WP_095957881.1\|2265794_2266319_-	hypothetical protein	NA	NA	NA	NA
WP_095957882.1\|2266318_2266957_-	hypothetical protein	NA	NA	NA	NA
WP_095957883.1\|2266958_2267336_-	hypothetical protein	NA	NA	NA	NA
WP_095957884.1\|2267673_2268285_-\|capsid	phage major capsid protein	A0A1B1P7E3	Bacillus_phage	8.0e-35	42.3
WP_095957885.1\|2268330_2269023_-	hypothetical protein	NA	NA	NA	NA
WP_095957886.1\|2269019_2270372_-	DNA adenine methylase	A0A1B1P7E4	Bacillus_phage	4.4e-17	38.3
WP_095957887.1\|2270364_2270544_-	hypothetical protein	NA	NA	NA	NA
WP_095957888.1\|2270599_2271679_-\|head	head morphogenesis protein	NA	NA	NA	NA
WP_095957889.1\|2271659_2271941_-	hypothetical protein	NA	NA	NA	NA
WP_095957890.1\|2271937_2273737_-\|portal	phage portal protein	A0A0U3E050	Pseudomonas_phage	1.3e-51	30.1
WP_095957891.1\|2273733_2273937_-	hypothetical protein	NA	NA	NA	NA
WP_157757482.1\|2274690_2275944_-	hypothetical protein	NA	NA	NA	NA
WP_157757483.1\|2275940_2276279_-	hypothetical protein	NA	NA	NA	NA
WP_170114807.1\|2276551_2277115_-\|terminase	terminase	A0A1B0T6F0	Thiobacimonas_phage	6.3e-10	30.1
WP_095957894.1\|2278066_2278681_+\|integrase	tyrosine-type recombinase/integrase	NA	NA	NA	NA
2286953:2286968	attR	NA	NA	NA	NA

DBSCAN-SWA_3

2459833 : 2470750

Bacillus_thuringiensis_phage(14.29%)

tRNA

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_095958003.1\|2459833_2462758_+	response regulator	Q56AR1	Bacillus_thuringiensis_phage	3.1e-07	31.3
WP_013938648.1\|2462807_2463803_+\|tRNA	tRNA (adenosine(37)-N6)-threonylcarbamoyltransferase complex transferase subunit TsaD	A0A0R6PI74	Moraxella_phage	1.1e-73	46.0
WP_095958004.1\|2463816_2464674_+	16S rRNA (adenine(1518)-N(6)/adenine(1519)-N(6))- dimethyltransferase RsmA	E4ZFQ0	Streptococcus_phage	2.2e-14	33.1
WP_043710562.1\|2464677_2464956_-	hypothetical protein	NA	NA	NA	NA
WP_013938651.1\|2465166_2465811_+	deoxynucleoside kinase	A0A288TXV5	Enterococcus_phage	4.4e-15	33.5
WP_095958005.1\|2465975_2466893_+	3-methyl-2-oxobutanoate hydroxymethyltransferase	A0A0N7HVJ8	Ostreococcus_lucimarinus_virus	3.1e-46	37.6
WP_095958006.1\|2466895_2467774_+	pantoate--beta-alanine ligase	NA	NA	NA	NA
WP_095958007.1\|2467770_2468259_+	SsrA-binding protein SmpB	W5RAM5	Staphylococcus_phage	3.0e-32	49.3
WP_013938655.1\|2468292_2468814_+	hypothetical protein	NA	NA	NA	NA
WP_095958008.1\|2468821_2470750_-	protein kinase	A0A1D6Y713	Golden_Marseillevirus	1.6e-12	26.0

DBSCAN-SWA_4

5533383 : 5564684

Stx2-converting_phage(25.0%)

transposase,plate,tail

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_157757535.1\|5533383_5535072_+\|transposase	IS66 family transposase	A0A0P0ZEB3	Stx2-converting_phage	1.0e-47	32.0
WP_095959539.1\|5535139_5535421_+	hypothetical protein	NA	NA	NA	NA
WP_095959541.1\|5536147_5537515_-	radical SAM protein	NA	NA	NA	NA
WP_095959542.1\|5537936_5539103_+	serine/threonine protein kinase	A0A2P1EM68	Moumouvirus	1.0e-09	28.4
WP_095959543.1\|5539125_5539473_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_095961659.1\|5539586_5539889_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_095959544.1\|5540019_5541936_+	serine/threonine protein kinase	A0A1C9C556	Heterosigma_akashiwo_virus	1.0e-06	24.7
WP_095959545.1\|5541945_5542872_+	DUF2381 family protein	NA	NA	NA	NA
WP_157757536.1\|5543134_5543779_-	hypothetical protein	NA	NA	NA	NA
WP_095959547.1\|5545000_5549260_+	DUF4157 domain-containing protein	NA	NA	NA	NA
WP_095959548.1\|5549603_5550611_+	pentapeptide repeat-containing protein	NA	NA	NA	NA
WP_123784252.1\|5550891_5551356_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_095959549.1\|5551352_5552084_+	hypothetical protein	NA	NA	NA	NA
WP_095959550.1\|5552139_5554512_+\|tail	phage tail sheath subtilisin-like domain-containing protein	H6WFT7	Cyanophage	3.1e-18	34.6
WP_013941083.1\|5554530_5554986_+\|tail	phage tail protein	NA	NA	NA	NA
WP_095959551.1\|5555014_5556586_+\|tail	phage tail sheath protein	NA	NA	NA	NA
WP_013941085.1\|5556582_5557062_+\|tail	phage tail protein	NA	NA	NA	NA
WP_095959552.1\|5557068_5558427_+	hypothetical protein	NA	NA	NA	NA
WP_170114757.1\|5558430_5558604_+	hypothetical protein	NA	NA	NA	NA
WP_095959553.1\|5558622_5559699_+	phage late control D family protein	NA	NA	NA	NA
WP_095959554.1\|5559695_5560394_+	hypothetical protein	NA	NA	NA	NA
WP_095959555.1\|5560324_5561932_+	hypothetical protein	NA	NA	NA	NA
WP_013941091.1\|5561939_5562341_+	GPW/gp25 family protein	NA	NA	NA	NA
WP_095959556.1\|5562341_5564684_+\|plate	putative baseplate assembly protein	NA	NA	NA	NA

DBSCAN-SWA_5

5915480 : 5950126

Agrobacterium_phage(50.0%)

plate,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_095959738.1\|5915480_5916848_+\|plate	type VI secretion system baseplate subunit TssK	NA	NA	NA	NA
WP_013941366.1\|5916863_5917580_+	DotU family type IV/VI secretion system protein	NA	NA	NA	NA
WP_043711753.1\|5917576_5921272_+	type VI secretion system membrane subunit TssM	NA	NA	NA	NA
WP_095961667.1\|5921273_5922206_+	type VI secretion system-associated protein TagF	NA	NA	NA	NA
WP_095959739.1\|5922211_5924188_+	type VI secretion system protein TssA	NA	NA	NA	NA
WP_013941370.1\|5924270_5924765_+	type VI secretion system contractile sheath small subunit	NA	NA	NA	NA
WP_013941371.1\|5924790_5926275_+	type VI secretion system contractile sheath large subunit	NA	NA	NA	NA
WP_013941372.1\|5926394_5926886_+	type VI secretion system tube protein Hcp	NA	NA	NA	NA
WP_013941373.1\|5926968_5927364_+\|plate	type VI secretion system baseplate subunit TssE	NA	NA	NA	NA
WP_013941374.1\|5927400_5929152_+\|plate	type VI secretion system baseplate subunit TssF	NA	NA	NA	NA
WP_095959740.1\|5929187_5930159_+\|plate	type VI secretion system baseplate subunit TssG	NA	NA	NA	NA
WP_095959741.1\|5930199_5932848_+	type VI secretion system ATPase TssH	A0A1S6UBG5	Serratia_phage	9.0e-99	34.8
WP_095959742.1\|5932856_5933891_+	hypothetical protein	NA	NA	NA	NA
WP_013941378.1\|5934041_5934407_+	HPF/RaiA family ribosome-associated protein	NA	NA	NA	NA
WP_095959743.1\|5934470_5935022_+	redoxin domain-containing protein	NA	NA	NA	NA
WP_095959744.1\|5935044_5936409_-	glycoside hydrolase family 16 protein	NA	NA	NA	NA
WP_095959745.1\|5936504_5937572_-	sulfate/molybdate ABC transporter ATP-binding protein	G9BWD6	Planktothrix_phage	5.7e-20	32.6
WP_043713548.1\|5937568_5938417_-	sulfate ABC transporter permease subunit CysW	NA	NA	NA	NA
WP_095959746.1\|5938422_5939265_-	sulfate ABC transporter permease subunit CysT	NA	NA	NA	NA
WP_095959747.1\|5939275_5940286_-	sulfate ABC transporter substrate-binding protein	NA	NA	NA	NA
WP_095959748.1\|5940613_5943208_+	LamG domain-containing protein	NA	NA	NA	NA
WP_095959749.1\|5943273_5946708_+\|protease	ATP-dependent Clp protease ATP-binding subunit	A0A223W0B1	Agrobacterium_phage	2.3e-54	30.0
WP_095959750.1\|5946712_5950126_+\|protease	ATP-dependent Clp protease ATP-binding subunit	A0A223W0B1	Agrobacterium_phage	3.2e-64	29.5

DBSCAN-SWA_6

6168106 : 6246170

Streptomyces_phage(14.29%)

transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_095961673.1\|6168106_6169255_-\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_095961674.1\|6169420_6171589_+	decarboxylase	NA	NA	NA	NA
WP_095959860.1\|6171794_6172529_-	endonuclease/exonuclease/phosphatase family protein	A0A2L1IVW7	Streptomyces_phage	4.2e-14	27.9
WP_095959861.1\|6172873_6173953_-	phosphomevalonate kinase	NA	NA	NA	NA
WP_095959862.1\|6173952_6174939_-	diphosphomevalonate decarboxylase	NA	NA	NA	NA
WP_095959863.1\|6174947_6175880_-	mevalonate kinase	NA	NA	NA	NA
WP_095959864.1\|6175884_6177213_-	hydroxymethylglutaryl-CoA reductase, degradative	NA	NA	NA	NA
WP_013941567.1\|6177246_6178305_-	type 2 isopentenyl-diphosphate Delta-isomerase	NA	NA	NA	NA
WP_095961675.1\|6178491_6178878_+	hypothetical protein	NA	NA	NA	NA
WP_095959865.1\|6178911_6181419_-	TonB-dependent receptor	NA	NA	NA	NA
WP_095959866.1\|6181530_6183009_-	hypothetical protein	NA	NA	NA	NA
WP_170114767.1\|6183197_6184430_+	imelysin family protein	NA	NA	NA	NA
WP_095959868.1\|6184422_6185877_+	HTTM domain-containing protein	NA	NA	NA	NA
WP_095959869.1\|6186043_6187027_+\|protease	zinc metalloprotease HtpX	NA	NA	NA	NA
WP_095959870.1\|6187188_6188214_+	cell envelope biogenesis protein TolA	NA	NA	NA	NA
WP_095959871.1\|6188295_6188751_-	MarR family transcriptional regulator	NA	NA	NA	NA
WP_095959872.1\|6188873_6190262_+	TolC family protein	NA	NA	NA	NA
WP_095959873.1\|6190249_6191410_+	efflux RND transporter periplasmic adaptor subunit	NA	NA	NA	NA
WP_095959874.1\|6191432_6194579_+	multidrug efflux RND transporter permease subunit	NA	NA	NA	NA
WP_013941579.1\|6195678_6197226_+	HAMP domain-containing sensor histidine kinase	W8CYF6	Bacillus_phage	4.6e-26	29.6
WP_095959875.1\|6197222_6198554_+	insulinase family protein	NA	NA	NA	NA
WP_095959876.1\|6198534_6199860_-	tetratricopeptide repeat protein	NA	NA	NA	NA
WP_013941582.1\|6199900_6200245_+	hypothetical protein	NA	NA	NA	NA
WP_095959877.1\|6200260_6201586_-	BamA/TamA family outer membrane protein	NA	NA	NA	NA
WP_095959878.1\|6201604_6202735_-	DUF819 family protein	NA	NA	NA	NA
WP_095959879.1\|6202731_6204048_-	aspartate aminotransferase family protein	NA	NA	NA	NA
WP_095959880.1\|6204356_6204794_-	DUF779 domain-containing protein	NA	NA	NA	NA
WP_095959881.1\|6204793_6206314_-	aldehyde dehydrogenase family protein	NA	NA	NA	NA
WP_095959882.1\|6206500_6208702_-	sigma-54-dependent Fis family transcriptional regulator	NA	NA	NA	NA
WP_095959883.1\|6208977_6210900_+	OmpA family protein	NA	NA	NA	NA
WP_095959884.1\|6210920_6215012_+	DUF4215 domain-containing protein	NA	NA	NA	NA
WP_095959885.1\|6215129_6218801_+	serine/threonine protein kinase	A0A2K9V9B7	Bandra_megavirus	4.4e-11	26.2
WP_170114768.1\|6218814_6219162_-	hypothetical protein	NA	NA	NA	NA
WP_095959887.1\|6219346_6220954_-	sigma-54-dependent Fis family transcriptional regulator	NA	NA	NA	NA
WP_095959888.1\|6221368_6222868_-	response regulator	NA	NA	NA	NA
WP_013941597.1\|6222887_6224738_-	response regulator	NA	NA	NA	NA
WP_013941598.1\|6224776_6225628_-	diaminopimelate epimerase	NA	NA	NA	NA
WP_095959889.1\|6225652_6231796_-	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_095959890.1\|6231783_6232737_+	IF-2 protein	NA	NA	NA	NA
WP_095959891.1\|6233176_6235693_+	ribonucleoside-diphosphate reductase subunit alpha	G3GQC5	Emiliania_huxleyi_virus	9.6e-183	45.1
WP_095959892.1\|6235768_6236779_+	ribonucleotide-diphosphate reductase subunit beta	R4ZDG8	Choristoneura_biennis_entomopoxvirus	6.8e-47	35.3
WP_095957122.1\|6237587_6239006_-\|transposase	ISKra4-like element ISMfu2 family transposase	NA	NA	NA	NA
WP_095959893.1\|6239339_6240750_+\|transposase	IS3 family transposase	U5P429	Shigella_phage	1.1e-10	25.6
WP_095959894.1\|6241839_6242799_+	SIR2 family protein	NA	NA	NA	NA
WP_095959895.1\|6242817_6243723_-\|transposase	IS4 family transposase	NA	NA	NA	NA
WP_095961422.1\|6243721_6244057_+	hypothetical protein	NA	NA	NA	NA
WP_013938504.1\|6244053_6244395_+	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_095961676.1\|6244472_6246170_+\|transposase	IS66 family transposase	A0A0P0ZEB3	Stx2-converting_phage	4.2e-41	29.4

DBSCAN-SWA_7

6415737 : 6461097

Vibrio_phage(25.0%)

transposase,tRNA,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_095959989.1\|6415737_6416772_-\|tRNA	tRNA pseudouridine(13) synthase TruD	NA	NA	NA	NA
WP_095959990.1\|6416768_6418112_-	DUF4388 domain-containing protein	NA	NA	NA	NA
WP_095959991.1\|6418119_6419100_-	thioredoxin domain-containing protein	NA	NA	NA	NA
WP_043713650.1\|6419172_6420234_+	asparaginase	NA	NA	NA	NA
WP_013941759.1\|6420294_6421206_+	GGDEF domain-containing protein	A0A127AWB9	Bacillus_phage	1.2e-21	35.5
WP_095959992.1\|6421271_6422885_-	HEAT repeat domain-containing protein	NA	NA	NA	NA
WP_002614080.1\|6422996_6423191_+	30S ribosomal protein S21	NA	NA	NA	NA
WP_013941762.1\|6423295_6423754_+	GatB/YqeY domain-containing protein	A0A292GL36	Xanthomonas_phage	1.0e-13	34.5
WP_050989256.1\|6424072_6425905_+	DNA primase	A0A1S5RF71	Helicobacter_phage	3.5e-41	32.9
WP_095959993.1\|6425997_6428124_+	RNA polymerase sigma factor RpoD	A0A2I7SAT0	Vibrio_phage	2.5e-35	36.7
WP_095959994.1\|6428205_6428592_+	MGMT family protein	NA	NA	NA	NA
WP_095959995.1\|6429130_6429385_-	hypothetical protein	NA	NA	NA	NA
WP_157770513.1\|6429384_6429696_-\|transposase	transposase	NA	NA	NA	NA
WP_157757553.1\|6429922_6431173_-	hypothetical protein	NA	NA	NA	NA
WP_095959997.1\|6431727_6432438_-	site-specific DNA-methyltransferase	A0A2I7R760	Vibrio_phage	2.5e-19	28.8
WP_095959998.1\|6433224_6433704_-	ATP-binding protein	NA	NA	NA	NA
WP_095961512.1\|6434222_6435920_-\|transposase	IS66 family transposase	A0A0P0ZEB3	Stx2-converting_phage	1.8e-39	29.3
WP_013938504.1\|6435997_6436339_-	IS66 family insertion sequence element accessory protein TnpB	NA	NA	NA	NA
WP_082207158.1\|6436335_6436671_-	hypothetical protein	NA	NA	NA	NA
WP_157757554.1\|6436857_6438153_-	hypothetical protein	NA	NA	NA	NA
WP_170114826.1\|6438460_6438631_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_157757555.1\|6439047_6439284_+	hypothetical protein	NA	NA	NA	NA
WP_157757556.1\|6439860_6440319_+	hypothetical protein	NA	NA	NA	NA
WP_095960002.1\|6440607_6440802_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_095957569.1\|6440928_6442508_-\|transposase	IS3 family transposase	A0A2P1JR32	Mycobacterium_phage	3.6e-10	28.4
WP_095960003.1\|6443173_6444340_+	hypothetical protein	NA	NA	NA	NA
WP_095960004.1\|6444419_6445340_-	hypothetical protein	NA	NA	NA	NA
WP_095960005.1\|6445803_6445920_-	hypothetical protein	NA	NA	NA	NA
WP_043711956.1\|6446295_6447123_+	hypothetical protein	NA	NA	NA	NA
WP_157757558.1\|6447262_6448174_+	hypothetical protein	NA	NA	NA	NA
WP_095960007.1\|6448370_6448694_-	DUF3175 domain-containing protein	A0A0F6TH17	Sinorhizobium_phage	2.0e-21	61.1
WP_095960008.1\|6449013_6449595_-	hypothetical protein	NA	NA	NA	NA
WP_170114770.1\|6449670_6451095_-	GTPase HflX	NA	NA	NA	NA
WP_095960010.1\|6451233_6452142_+\|protease	CPBP family intramembrane metalloprotease	NA	NA	NA	NA
WP_095960011.1\|6452182_6453088_+	RluA family pseudouridine synthase	NA	NA	NA	NA
WP_157757559.1\|6453101_6454088_-	hypothetical protein	NA	NA	NA	NA
WP_157757560.1\|6454084_6456157_-	hypothetical protein	NA	NA	NA	NA
WP_095961506.1\|6456304_6457510_+\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_095960014.1\|6457533_6458034_-	hypothetical protein	NA	NA	NA	NA
WP_095960015.1\|6458790_6460209_+	hypothetical protein	NA	NA	NA	NA
WP_095960016.1\|6460326_6461097_+\|protease	protease	NA	NA	NA	NA

DBSCAN-SWA_8

7495299 : 7522974

Leptospira_phage(25.0%)

transposase,protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_095960583.1\|7495299_7495518_+\|transposase	IS3 family transposase	NA	NA	NA	NA
WP_095960584.1\|7495551_7496685_+	alpha/beta hydrolase	NA	NA	NA	NA
WP_157757577.1\|7496818_7497574_+	RICIN domain-containing protein	NA	NA	NA	NA
WP_095960586.1\|7497648_7498518_-	class I SAM-dependent methyltransferase	NA	NA	NA	NA
WP_095960587.1\|7498980_7500231_+	SBBP repeat-containing protein	S5WIY5	Leptospira_phage	1.1e-41	31.2
WP_095960588.1\|7500302_7502132_-\|protease	aspartyl protease family protein	NA	NA	NA	NA
WP_095960589.1\|7502128_7502962_-	TrmB family transcriptional regulator	NA	NA	NA	NA
WP_095960590.1\|7503282_7505169_-	chloride channel protein	NA	NA	NA	NA
WP_095960591.1\|7505155_7505638_-	MarR family transcriptional regulator	NA	NA	NA	NA
WP_095960592.1\|7506223_7507693_-	endo alpha-1,4 polygalactosaminidase	NA	NA	NA	NA
WP_095960593.1\|7507970_7509233_-	phosphatidylserine decarboxylase family protein	A0A2K9L169	Tupanvirus	1.0e-20	33.0
WP_095958729.1\|7509326_7510568_+\|transposase	IS256 family transposase	A0A2P1JQX9	Mycobacterium_phage	2.0e-72	40.1
WP_013938066.1\|7510743_7511667_-	hypothetical protein	NA	NA	NA	NA
WP_095961738.1\|7512535_7513126_-	Uma2 family endonuclease	NA	NA	NA	NA
WP_170114789.1\|7513372_7514314_-	LysR family transcriptional regulator	NA	NA	NA	NA
WP_095961739.1\|7514386_7514959_+	AhpC/TSA family protein	NA	NA	NA	NA
WP_157757578.1\|7515529_7515928_+\|transposase	transposase zinc-binding domain-containing protein	NA	NA	NA	NA
WP_095961741.1\|7516706_7518029_+	hypothetical protein	NA	NA	NA	NA
WP_095960596.1\|7518028_7519087_+	trypsin-like peptidase domain-containing protein	NA	NA	NA	NA
WP_095960598.1\|7519646_7521054_-\|transposase	IS3 family transposase	U5P429	Shigella_phage	9.9e-12	25.6
WP_095960599.1\|7521303_7522974_-\|transposase	ISL3 family transposase	NA	NA	NA	NA

DBSCAN-SWA_9

8934293 : 8967461

Salmonella_phage(33.33%)

transposase,tRNA,integrase

attL 8957819:8957847|attR 8968718:8968746

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_095961406.1\|8934293_8936141_-\|tRNA	tRNA uridine-5-carboxymethylaminomethyl(34) synthesis enzyme MnmG	NA	NA	NA	NA
WP_043709789.1\|8936898_8938146_+	multidrug effflux MFS transporter	S4TR35	Salmonella_phage	2.2e-23	30.1
WP_095961407.1\|8939431_8939686_+\|transposase	transposase	NA	NA	NA	NA
WP_095961408.1\|8939747_8940032_+	hypothetical protein	NA	NA	NA	NA
WP_095961409.1\|8940213_8940630_+	hypothetical protein	NA	NA	NA	NA
WP_013936858.1\|8940639_8940963_+	TIGR02996 domain-containing protein	NA	NA	NA	NA
WP_157770506.1\|8940919_8941267_-\|transposase	transposase	NA	NA	NA	NA
WP_095961411.1\|8941479_8942259_+	alpha/beta hydrolase	NA	NA	NA	NA
WP_095961412.1\|8942356_8942656_+	hypothetical protein	NA	NA	NA	NA
WP_095961413.1\|8942745_8945592_-	insulinase family protein	A0A167R9K4	Powai_lake_megavirus	7.1e-17	21.9
WP_095961414.1\|8945906_8947700_+	signal peptide peptidase SppA	NA	NA	NA	NA
WP_013936854.1\|8947775_8948369_-	cysteine dioxygenase family protein	NA	NA	NA	NA
WP_095961812.1\|8948664_8949876_+	general secretion pathway protein GspE	NA	NA	NA	NA
WP_043709780.1\|8950514_8950841_+	winged helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_013936850.1\|8950837_8951308_+	SRPBCC domain-containing protein	NA	NA	NA	NA
WP_013936849.1\|8951324_8951711_+	DoxX family protein	NA	NA	NA	NA
WP_050989280.1\|8951730_8952300_-	Uma2 family endonuclease	NA	NA	NA	NA
WP_095961415.1\|8952412_8953921_-\|tRNA	tRNA modification GTPase	NA	NA	NA	NA
WP_013936846.1\|8953993_8954221_-	hypothetical protein	NA	NA	NA	NA
WP_095961416.1\|8954269_8955049_-	hypothetical protein	NA	NA	NA	NA
WP_095961417.1\|8955045_8956860_-	membrane protein insertase YidC	NA	NA	NA	NA
WP_013936843.1\|8956909_8957128_-	membrane protein insertion efficiency factor YidD	NA	NA	NA	NA
WP_013936842.1\|8957124_8957547_-	ribonuclease P protein component	NA	NA	NA	NA
WP_002637840.1\|8957559_8957712_-	50S ribosomal protein L34	NA	NA	NA	NA
8957819:8957847	attL	NA	NA	NA	NA
WP_095961418.1\|8958112_8959915_-	serine/threonine protein kinase	NA	NA	NA	NA
WP_157770507.1\|8959946_8960807_-	DUF2381 family protein	NA	NA	NA	NA
WP_157770508.1\|8961034_8961580_+\|transposase	transposase family protein	NA	NA	NA	NA
WP_095961813.1\|8961821_8963099_+\|integrase,transposase	DDE-type integrase/transposase/recombinase	NA	NA	NA	NA
WP_095961814.1\|8963419_8964625_+\|transposase	IS701 family transposase	NA	NA	NA	NA
WP_095961421.1\|8965485_8965752_+	hypothetical protein	NA	NA	NA	NA
WP_095961676.1\|8965763_8967461_-\|transposase	IS66 family transposase	A0A0P0ZEB3	Stx2-converting_phage	4.2e-41	29.4
8968718:8968746	attR	NA	NA	NA	NA

Anti-CRISPR protein detection

Acr_ID: NZ_CP022203.1|WP_095959889.1|6225652_6231796_-|methyltransferase-domain-containing-protein

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Acr ID

Acr position

Acr size

Homology with known anti

Neighbor HTH/AcRanker

Neighbor Aca

In prophage

Protospacer in prophage

NZ_CP022203.1|WP_095959889.1|6225652_6231796_-|methyltransferase-domain-containing-protein

6225652_6231796_-

2047 aa aa

6168106-6246170

yes

CRISPR ID	CRISPR type	Spacer info	Spacer location	Spacer length	Protospacer location	Mismatch
NZ_CP022203_11	Orphan	11.10\|5517083\|19\|NZ_CP022203\|CRT	5517083-5517101	19	6187628-6187610	2

1. spacer 11.10|5517083|19|NZ_CP022203|CRT matches to NZ_CP022203 position: 6187628-6187610, mismatch: 2

ggcgcggcgggcgccggct	CRISPR spacer
ggcgcggccggcgcgggct	Protospacer
******** ***** ****

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP022203

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection

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