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_CP023690	Streptomyces spectabilis strain ATCC 27465 chromosome, complete genome	11 crisprs	RT,csa3,Cas9_archaeal,casR,DEDDh,WYL,cas4,cas6e,cas5,cas7,cse2gr11,cas8e,cas3,PD-DExK,DinG	0	23	6	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP023690_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_1

2160907-2161039

Orphan

Consensus_repeat	Method
AGCCCGTCCGGCGATTGAGGACGAGGCCGCAGGCCGA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_1

>merge|NZ_CP023690|1|2160907-2161039|CRISPRCasFinder
AGCCCGTCCGGCGATTGAGGACGAGGCCGCAGGCCGACCGACCCACTGGTGGCGGCATGGATGGCCCGCAGACAGAAGACCAGCAGCGGGAACTGAAGCCCGTCCGGCGATTGAGGACGAGGCCGCAGGCCGA

>NZ_CP023690|1|1|2160907-2161039|CRISPRCasFinder
AGCCCGTCCGGCGATTGAGGACGAGGCCGCAGGCCGA	CCGACCCACTGGTGGCGGCATGGATGGCCCGCAGACAGAAGACCAGCAGCGGGAACTGA
AGCCCGTCCGGCGATTGAGGACGAGGCCGCAGGCCGA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_138958637.1\|2158546_2159740_-\|argininosuccinate-synthase	unknown	unknown	gnl\|CDD\|234785
NZ_CP023690.1\|WP_030680925.1\|2161068_2161614_-\|arginine-repressor	unknown	unknown	gnl\|CDD\|235116
NZ_CP023690.1\|WP_150510049.1\|2153697_2155242_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|184957
NZ_CP023690.1\|WP_150510056.1\|2163861_2165013_-\|bifunctional-glutamate-N-acetyltransferase/amino-acid-acetyltransferase-ArgJ	unknown	unknown	gnl\|CDD\|235441
NZ_CP023690.1\|WP_150510045.1\|2149724_2150156_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510057.1\|2165009_2166038_-\|N-acetyl-gamma-glutamyl-phosphate-reductase	unknown	unknown	gnl\|CDD\|234761
NZ_CP023690.1\|WP_150510051.1\|2155921_2156899_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381324
NZ_CP023690.1\|WP_150510058.1\|2166224_2168444_-\|NADP-dependent-isocitrate-dehydrogenase	unknown	unknown	gnl\|CDD\|377178
NZ_CP023690.1\|WP_144002441.1\|2152935_2153625_+\|1-acyl-sn-glycerol-3-phosphate-acyltransferase	unknown	unknown	gnl\|CDD\|153251
NZ_CP023690.1\|WP_150510059.1\|2168573_2169050_-\|MerR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|133384
NZ_CP023690.1\|WP_150510046.1\|2150163_2150688_-\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379228
NZ_CP023690.1\|WP_150510052.1\|2157022_2158453_-\|argininosuccinate-lyase	unknown	unknown	gnl\|CDD\|179143
NZ_CP023690.1\|WP_150510055.1\|2162877_2163795_-\|acetylglutamate-kinase	unknown	unknown	gnl\|CDD\|234869
NZ_CP023690.1\|WP_150510060.1\|2169048_2170014_+\|SDR-family-NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|235736
NZ_CP023690.1\|WP_150510061.1\|2170036_2171584_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|312032
NZ_CP023690.1\|WP_150510062.1\|2171849_2172839_+\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381302
NZ_CP023690.1\|WP_150510047.1\|2150728_2151253_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP023690.1\|WP_170316627.1\|2155238_2155817_-\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP023690.1\|WP_150510054.1\|2161621_2162881_-\|acetylornithine-transaminase	unknown	unknown	gnl\|CDD\|235112
NZ_CP023690.1\|WP_150510048.1\|2151327_2152518_-\|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl\|CDD\|176544

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_138958637.1\|2158546_2159740_-\|argininosuccinate-synthase	gnl\|CDD\|234785	PRK00509, PRK00509, argininosuccinate synthase; Provisional.	0
NZ_CP023690.1\|WP_030680925.1\|2161068_2161614_-\|arginine-repressor	gnl\|CDD\|235116	PRK03341, PRK03341, arginine repressor; Provisional.	1.94108e-87
NZ_CP023690.1\|WP_150510049.1\|2153697_2155242_-\|MFS-transporter	gnl\|CDD\|184957	PRK14995, PRK14995, SmvA family efflux MFS transporter.	6.44881e-106
NZ_CP023690.1\|WP_150510056.1\|2163861_2165013_-\|bifunctional-glutamate-N-acetyltransferase/amino-acid-acetyltransferase-ArgJ	gnl\|CDD\|235441	PRK05388, argJ, bifunctional glutamate N-acetyltransferase/amino-acid acetyltransferase ArgJ.	0
NZ_CP023690.1\|WP_150510057.1\|2165009_2166038_-\|N-acetyl-gamma-glutamyl-phosphate-reductase	gnl\|CDD\|234761	PRK00436, argC, N-acetyl-gamma-glutamyl-phosphate reductase; Validated.	1.80165e-178
NZ_CP023690.1\|WP_150510051.1\|2155921_2156899_-\|aldo/keto-reductase	gnl\|CDD\|381324	cd19098, AKR_unchar, uncharacterized aldo-keto reductase (AKR) superfamily protein. This family includes a group of uncharacterized AKR superfamily proteins. Aldo-keto reductases (AKRs) are a superfamily of soluble NAD(P)(H) oxidoreductases whose chief purpose is to reduce aldehydes and ketones to primary and secondary alcohols. AKRs are present in all phyla and are of importance in both health and industrial applications.	1.34368e-138
NZ_CP023690.1\|WP_150510058.1\|2166224_2168444_-\|NADP-dependent-isocitrate-dehydrogenase	gnl\|CDD\|377178	pfam03971, IDH, Monomeric isocitrate dehydrogenase. NADP(+)-dependent isocitrate dehydrogenase (ICD) is an important enzyme of the intermediary metabolism, as it controls the carbon flux within the citric acid cycle and supplies the cell with 2-oxoglutarate EC:1.1.1.42 and NADPH for biosynthetic purposes.	0
NZ_CP023690.1\|WP_144002441.1\|2152935_2153625_+\|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.	5.48189e-52
NZ_CP023690.1\|WP_150510059.1\|2168573_2169050_-\|MerR-family-transcriptional-regulator	gnl\|CDD\|133384	cd01109, HTH_YyaN, Helix-Turn-Helix DNA binding domain of the MerR-like transcription regulators YyaN and YraB. Putative helix-turn-helix (HTH) MerR-like transcription regulators of Bacillus subtilis, YyaN and YraB, and related proteins; N-terminal domain. Based on sequence similarity, these proteins are predicted to function as transcription regulators that mediate responses to stress in eubacteria. They belong to the MerR superfamily of transcription regulators that promote transcription of various stress regulons by reconfiguring the operator sequence located between the -35 and -10 promoter elements. A typical MerR regulator is comprised of distinct domains that harbor the regulatory (effector-binding) site and the active (DNA-binding) site. Their N-terminal domains are homologous and contain a DNA-binding winged HTH motif, while the C-terminal domains are often dissimilar and bind specific coactivator molecules such as metal ions, drugs, and organic substrates.	7.17248e-41
NZ_CP023690.1\|WP_150510046.1\|2150163_2150688_-\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.97908e-11
NZ_CP023690.1\|WP_150510052.1\|2157022_2158453_-\|argininosuccinate-lyase	gnl\|CDD\|179143	PRK00855, PRK00855, argininosuccinate lyase; Provisional.	0
NZ_CP023690.1\|WP_150510055.1\|2162877_2163795_-\|acetylglutamate-kinase	gnl\|CDD\|234869	PRK00942, PRK00942, acetylglutamate kinase; Provisional.	1.03404e-148
NZ_CP023690.1\|WP_150510060.1\|2169048_2170014_+\|SDR-family-NAD(P)-dependent-oxidoreductase	gnl\|CDD\|235736	PRK06196, PRK06196, oxidoreductase; Provisional.	4.67331e-160
NZ_CP023690.1\|WP_150510061.1\|2170036_2171584_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|312032	pfam08386, Abhydrolase_4, TAP-like protein. This is a family of putative bacterial peptidases and hydrolases that bear similarity to a tripeptidyl aminopeptidase isolated from Streptomyces lividans. A member of this family is thought to be involved in the C-terminal processing of propionicin F, a bacteriocidin characterized from Propionibacterium freudenreichii.	1.05895e-14
NZ_CP023690.1\|WP_150510062.1\|2171849_2172839_+\|aldo/keto-reductase	gnl\|CDD\|381302	cd19076, AKR_AKR13A_13D, AKR13A and AKR13D families of aldo-keto reductase (AKR). Schizosaccharomyces pombe aldo-keto reductase YakC is a founding member of aldo-keto reductase family 13 member A1 (AKR13A1). It catalyzes the reversible reduction of ketones to the respective alcohols using NADP(+) as a hydride donor. Rauvolfia serpentina PR is a founding member of aldo-keto reductase family 13 member D1 (AKR13D1). It catalyzes the NADPH-dependent reduction of the aldehyde perakine to yield the alcohol raucaffrinoline in the biosynthetic pathway of ajmaline in Rauvolfia, a key step in indole alkaloid biosynthesis. This family also includes Arabidopsis thaliana aldo-keto reductases, ALKR1-6.	6.87009e-180
NZ_CP023690.1\|WP_150510047.1\|2150728_2151253_-\|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.	1.78945e-14
NZ_CP023690.1\|WP_170316627.1\|2155238_2155817_-\|TetR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	3.83592e-09
NZ_CP023690.1\|WP_150510054.1\|2161621_2162881_-\|acetylornithine-transaminase	gnl\|CDD\|235112	PRK03244, argD, acetylornithine transaminase.	0
NZ_CP023690.1\|WP_150510048.1\|2151327_2152518_-\|glycerophosphodiester-phosphodiesterase	gnl\|CDD\|176544	cd08602, GDPD_ScGlpQ1_like, Glycerophosphodiester phosphodiesterase domain of Streptomycin coelicolor (GlpQ1) and similar proteins. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in a group of putative bacterial and eukaryotic glycerophosphodiester phosphodiesterases (GP-GDE, EC 3.1.4.46) similar to Escherichia coli periplasmic phosphodiesterase GlpQ, as well as plant glycerophosphodiester phosphodiesterases (GP-PDEs), all of which catalyzes the Ca2+-dependent degradation of periplasmic glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols. The prototypes of this family include putative secreted phosphodiesterase encoded by gene glpQ1 (SCO1565) from the pho regulon in Streptomyces coelicolor genome, and in plants, two distinct Arabidopsis thaliana genes, AT5G08030 and AT1G74210, coding putative GP-PDEs from the cell walls and vacuoles, respectively.	1.52493e-154

>NZ_CP023690.1|WP_138958637.1|2158546_2159740_-|argininosuccinate-synthase
MTERVVLAYSGGLDTSVAIGWIAEETGAEVIAVAVDVGQGGEDLDVIRKRALACGAVEAEVADAKDEFADEYCLPAIKANALYMDRYPLVSALSRPTIVKHLVAAANKHGAGIVAHGCTGKGNDQVRFEAGIQALGPDLKCIAPVRDYAMTRDKAIAFCEDKGLPIATSKKSPYSIDQNVFGRAVETGFLEDIWNAPIEDVYEYTSNPATPREADEVVLTFKEGVPVAIDGRPVTVLQAIQQLNERAGAQGIGRIDMVEDRLVGIKSREVYEAPGAIALITAHQELENVTVERELARYKRQVEQRWGELVYDGLWFSPLKRALDGFINEANQHVSGDIRMTLHGGRAVVTGRKSEQSLYDFNLATYDTGDTFDQSKAQGFIDIFALSSKIAAKRDLA
>NZ_CP023690.1|WP_150510052.1|2157022_2158453_-|argininosuccinate-lyase
MSSNSGDVRLWGGRFADGPAEALARLSASVHFDWRLAPYDIAGSRAHARVLHTAGLLTADELERMLAGLDLLEGDVASGAFVGTVADEDVHTALERGLLERLGPDLGGKLRAGRSRNDQVATLFKMYLRDHARIIGGLVTDLQEALIGLAEAHPDVAMPGRTHLQHAQPVLFAHHVLAHVQSLSRDAERLRQWDERTAVSPYGSGALAGSSLGLDPEAVARDLGFEHGSAANSIDGTASRDFVAEFAFITAMIGVNLSRIAEEVIIWNTKEFSFVTLHDAFSTGSSIMPQKKNPDIAELARGKSGRLIGNLTGLMATLKALPLAYNRDLQEDKEPVFDSCDQLEVLLPAFTGMMATLTVNRERMEELAPAGFSLATDIAEWLVKQGVPFRVAHEVAGSCVKECEAQGIELDQLTDEQFAKISPHLTPEVRTVLNVPGALASRDGRGGTAPSAVAVQLAEIKTDVAAQRRWATARTA
>NZ_CP023690.1|WP_150510051.1|2155921_2156899_-|aldo/keto-reductase
MPFARLAEATTPTAHIGLGLAAVGRPGYITLGREADLPPSRSVEALRERAFELLDAAYALGVRYVDAARSYGRSEEFLADWLASRPAADTADVVVGSKWGYTYTADWRTDATAHEVKDHSVAAYDRQRAETAALLGGRLDLYQIHSVTPGSPALTDKELHARLADLAAEGVTVGLSVSGPEQAAAIRAALDVTVGGAPLFRTVQATYNALETSAGPALAEAHDAGLTVLVKEGMANGRLAGEHAPAALRAVAERTGLGCDAVALALVLREPWAGVVLSGAATSVQLVSNLHAAAVDLDAEDLERAGALAEEPAAYWSTRAALPWH
>NZ_CP023690.1|WP_170316627.1|2155238_2155817_-|TetR-family-transcriptional-regulator
MSHVVYGCLMSVDRDQVLRGAAALLTRKGSATMDEVAKAAGVSRATLHRHFAGRDALVRALEDLGLRECELALDAARLDEGGAADALRRLVKELQPAAGLLAFLVTENALFEGESQHEGWSRIDTRVAELFRRGQESGEFRIDLTPVWLTEALYGLVSSGAWAVLDGRVASKDFSYMIAELLIGGARRRVEP
>NZ_CP023690.1|WP_150510049.1|2153697_2155242_-|MFS-transporter
MTRTAQRTSPTEVARPPGRWLALAVLVLAVLLVAVDATVLGLATPYISEDLKPSGNQLLWIGDVYSFVIAGLLVSMGSLGDRIGRKKLLLVGAVAFGAVSVLNSYATTPELMILARALLGVAGATLMPSTLALIRNIFHDPRERSIAVGVWGAMASAGAAIGPVVGGFLLEHFWWGSVFLINLPVMAVLVLVGIKLLPESKNPAPGPWDLISVALSLIGMIAVVYAVKEAAATGAGWEVFAAGAVGVGALTWFVRRQLTLQAPLLDMRLFRNRGFSAAVLADLLTILGLSGLVFFLSQFLQLVQGRQPFEAGLAELPAALGAVTAGLIAGLVARRFSVRAVVAGGLAAVGLALASLTTLSQHTGYPLLGAALLVVGVGAGFSFTVTADVILSSVPKEQAGAASAVSETAYELGAALGIALLGSIVTGVYRDFTAPAGTPADVASAAHESLGGAVEASAGLPAHTAGPLVSAAQDAFVDGLRVAAGVGAAVLLATAVAAWFLLKGQKLDDGVEHP
>NZ_CP023690.1|WP_144002441.1|2152935_2153625_+|1-acyl-sn-glycerol-3-phosphate-acyltransferase
MTPEEPLSRLALLKAVLGPILRLTFRTRVEGAENIPGTGPVILAGNHLTFIDSMILPVVCDRAVYFIGKDEYVTGKGLKGRLMAWFFTGVGMIPVDRDGGRGGVAALMTGKRVLDDGQMFGIYPEGTRSPDGRLYRGRTGIARLTLMTGAPVVPFAMIGTDKLQPGGKGLPRPGRVTVRFGEAMEFSRYDGMDRDRYVLRAVTDSVMTEVMRLSGQEYVDMYATKAKAA
>NZ_CP023690.1|WP_150510048.1|2151327_2152518_-|glycerophosphodiester-phosphodiesterase
MANEEYGATAERRTGTSPGRRAVLGAAVLGAGAAVAGAPGVARAEGRHGHGHGGDLPVPTVIAHRGTSGYRPEHTLGSYQLALDMGADVIEQDVVPTKDGHLVCRHENDITATTDVAAHPEFADRKTTKSVDGAQLTGWFTEDFTLAELKTLRAKERIPGTRQRNTLYDGRWEVPTLEEVLRWAERAGRERGRRVWLHIETKHPTYFRKLGLGLEEPLAKLLRRYNRHRRHSPNFLQSFEPSSIQRLRKLVDAPGVVLLSTANSRPWDFVEANDPRTVADLIKPEGLRWMASYAKGIGPTLDLIIPKGPDGKLLEPTTLVRDAHAADLILHPYTMRNENTFLPADFKKGTDPTAYGDAFGAFKKYFATGIDGIFSDNPDTALLAAADFRAGGSVNE
>NZ_CP023690.1|WP_150510047.1|2150728_2151253_-|sigma-70-family-RNA-polymerase-sigma-factor
MTPSLSPDLVTALRPLLAAEASAEAHGSGAEPGDLEQAVWLRLLEHLDAKGSLTDPADWLRAAVRDEAHRSRHTARRERPYVTEPADDLQGGPEQRVLRADRHRILRAAVRKLPGRCPRLLAALLSPKDLTYREIAGELGMSQGSLGPERSRCLGCLRRMLAQEVATPGPWGKE
>NZ_CP023690.1|WP_150510046.1|2150163_2150688_-|GNAT-family-N-acetyltransferase
MGMSVTISEAAADDQDAAEQILKLQYLCYQSEAELYGDYSIEPLTQSLDSLKAELAGGTVLVARLGTEVVASVRASVDGTGTARVGKLVVHPRMQRHGLGGRLLDAIERRLGEGGAARRFELFTGHRSESNLQLYRKHGYAPVSTRRVDEKLTVVTLAKDATDAAPAPAFVASA
>NZ_CP023690.1|WP_150510045.1|2149724_2150156_+|hypothetical-protein
MTASGKAPEQDGPKRQKLISGPGILLVWLYGVMVVGAVSRSAVQIATDFDRAPLAYTLSALAGVVYGFITYSLVRGGETARRAALVCCAAELVGVLGVGAWTLAEPSAFPDATVWSDFGMGYLFIPVLLPVTALYWLRRSRRP
>NZ_CP023690.1|WP_030680925.1|2161068_2161614_-|arginine-repressor
MSHAQRNERGESAGPAVPQTRTARHRRIVDILNRQPVRSQSQLAKLLADDGLSVTQATLSRDLDELNAVKIRNAEGDLIYAVPSEGGFRTPRAPLGESAKEERMRRLSGELLISAEASANLVVLRTPPGAAQFLASAIDQAELHDILGTIAGDDTVMLISRDATGGQALADHLLRLASNEH
>NZ_CP023690.1|WP_150510054.1|2161621_2162881_-|acetylornithine-transaminase
MTAATPSTPSTPSTPAPSFNASLTARWQGALMDNYGTPRLPLVRGAGSRLWDADGKEYVDFVGGIAVNALGHGHPAVVDAVSRQIAALGHVSNLFVAEPPVALAERLLQLFGRDGRVYFCNSGAEANEGAFKIGRLTGRPHMVATEGGFHGRTMGALALTGQPGKQQPFLPLPGDVTHVPYGDVDALRAAVTEDTAFVIIEPIQGENGAVVPPAGYLRAAREITRATGTLLVLDEVQTGVGRTGHWFAHFAEEDVLPDVVTLAKGLGGGLPLGATVAFGAAAELLRPGHHGTTFGGNPVACAAGLAVLDTITAEGLLDRTKRAGERLRHGIESAGHGMVDHVRGAGLLLGMVLTEPLAAQVQQAAQDAGFLVNAPAPDVVRLMPALNVGDTEVDAFLRALPGVLDQAAAAANGDGRSGE
>NZ_CP023690.1|WP_150510055.1|2162877_2163795_-|acetylglutamate-kinase
MSTRKHTALPKAQTLIEALPWLTRHRGKTVVIKFGGNAMVDAELKAAFAQDVVFLHHAGLRPVVVHGGGPQISAQLDKQGLVSEFKAGLRVTTPEAMDVVRMVLAGQVQRELVGLLNEHGPLAVGLTGEDAHTITATRHRPLIDGEPVDIGRVGEVTDIDTGAIQALLTDGRIPVVSSIARSQDEGDTGHVYNVNADTAAAALAAALGAETLMVLTDVEGLYEDWPRSDDVISRLTATELEKLLPELSSGMVPKMRGCLHAVRNGVQTARVIDGRVQHSILLEIFTDEGIGTMVVPDAPTEGATA
>NZ_CP023690.1|WP_150510056.1|2163861_2165013_-|bifunctional-glutamate-N-acetyltransferase/amino-acid-acetyltransferase-ArgJ
MSVTAAKGFQAAGIAAGIKENGNPDLALVVNSGPRRAAAGVFTSNRVKAAPVLWSEQVLKGGQVAAVVLNSGGANACTGPKGFQDTHATAEKAAEALGVDAAEVAVASTGLIGVTLPMDKLLPGVEAAAAALSPHGGEKAAIAIKTTDSVHKTAVFEGEGWTVGGMAKGAGMLAPGLATMLVVLTTDADLPAADLDKALREATRLTFDRVDSDGCMSTNDTVLLLASGAADVTPGQAEFAEAVRGVCDDLARQLIGDAEGASKDIRIEVVGAASEDDAVEVGRSIARNNLLKCAIHGEDPNWGRVLSAIGTTGAAFEPDRLNVAINDVWVCKNGSVGEDRDLVDMRYREVKITADLAAGSESAVIWANDLTADYVHENSAYSS
>NZ_CP023690.1|WP_150510057.1|2165009_2166038_-|N-acetyl-gamma-glutamyl-phosphate-reductase
MTVRAAVAGASGYAGGELLRTLLTHPEVEIGTLTANSNAGQPLGALQPHLTPLAERVLEPTTAETLAGHDVVFLALPHGQSAAVAEQLGPDVLVVDMGADFRLADAADWERFYGSEHAGTWPYGLPELPGARAALAGTKRIAVPGCYPTAVSLALFPAYAAGLVEDEAVIVAASGTSGAGKAAKPHLLGSEVMGSMSPYGVGGVHRHTPEMIQNLSAAAGTRVSVSFTPTLAPMPRGILATCSAKARPGVTAESVRATYEKAFADEPFVRLLPEGQWPATASVYGSNAVHVQVAHDPGSGRVIVISAIDNLTKGTAGGAVQSMNIALGLPEELGLSTIGVAP
>NZ_CP023690.1|WP_150510058.1|2166224_2168444_-|NADP-dependent-isocitrate-dehydrogenase
MTDSTIIYTHTDEAPALATHSFLPVIQAYASTAGVRVETRDISLAGRIIASFPERLEPSQRIEDALAELGELAKTPQANIIKLPNISASIPQLKAAVAELQEQGYALPDYPDDPKTDEERDIRARYDKVKGSAVNPVLREGNSDRRAPASVKNYAKTHPHRMGAWSADSKTNVATMGENDFRSTEKSAVVAEDGVLRIELAAADGTTTVLRESVPVLAGEVVDASVLHVAALREFLTAQIARAKAEGVLFSVHLKATMMKVSDPIIFGHVVRAFFPQTFEKYGDVLAGAGLTPNDGLGGIYKGLEALPNGAEIKASFDAELAAGPELAMVDSDRGITNLHVPSDVIVDASMPAMIRTSGHMWGPDGQEADTLAVLPDSSYAGIYQVVIDDCRANGAYDPATMGTVPNVGLMAQKAEEYGSHDKTFEVAAAGTVRLVDQQGNVVIEQAVAAGDIFRACQTKDAPIKDWVKLAVTRARATGDPAVFWLDEGRAHDAQLIAKVEQYLPEHDTEGLDIKILAPVDAIKFSVERIRRGENTISVTGNVLRDYLTDLFPILELGTSAKMLSVVPLMNGGGLFETGAGGSAPKHVQQLVKENYLRWDSLGEFLALAVSFEHLAQTTGNARAQVLADTLDRATASFLNENKSPSRKLGGIDNRGSHFYLSLYWAQELAKQTDDAQLAEAFGPLAKTLTEQERKIVDELVAVQGSPVDIGGYYKPDVTKAAAAMRPSATFNEAIASLA
>NZ_CP023690.1|WP_150510059.1|2168573_2169050_-|MerR-family-transcriptional-regulator
MAGTLEPRLRSRSSRARAEAKVAQRAEGKSIGQVARETGLSVHALRFFEREELFLRPVPRTGGGRRVYEPADVEWLLLCNRLRESGMPIATLKRFAGLVRSGPGNEPERLALLQEHERAVRAKLAELGASLEIIHGKVVAYERHVREGTATGVWAPGP
>NZ_CP023690.1|WP_150510060.1|2169048_2170014_+|SDR-family-NAD(P)-dependent-oxidoreductase
MTTKTAEQRGTGSGHGAWSTADDVLEGVSLKGRTALVTGGHSGLGLETTRALVRAGARVLVPARRPEAAATALGGLPGTEVAALDLADLDSVRAFADRVLDTGRALDLLIAGAGVMACPETRVGPGWEAHFAVNHLGHYALVNRLAPALSPGRARVVAVASSGHFLSDIRWADPHFHRGYDRWLAYAQSKTANALFALHLDRLAGSGGPRAFAVHPGSVLTPLQRHVPREEQLALGWVGADGTPAEGFKSPAQGAATAVWAATSPLLADRGGAYCQDCDVAGPATTDDMLVGGVKPWVRDPGSAARLWELSAELTGVDHFA
>NZ_CP023690.1|WP_150510061.1|2170036_2171584_-|alpha/beta-fold-hydrolase
MRAVTFTAAGLGLAALLAGGVPATAQPPDPAGGALAAYRNQHLTWGACSPGQKELRAAGARCADVTVPLDYAEPEGRTLTIAVSRIEAEAPAGERRGVLLSNPGGPGGLGLASTLALRPALKDVARAYDLIGFDPRFLGESTPLTCDPAREPAEPGPTTTPRRDFEESLAAAREDARRCHARGDNARLLPHASSRNVARDMDVIRAALGERRLSYYGVSYGADLGAAYTQMFPDRVDRFVVDSVTDPAATQYEQFQRSGGPAEAALDEWAAWTARRDSPYHLGRTAAAVRRQVESLLARAERRPLRVDGLRLNAPLLRMILKQPLVQAENDPTAAAVVRDLVAAAHGGTAEPGPELARMIELLKSPELADGMLGGMIFMCGDGGWPAGGWPGAPETYWRNSLRSRATEPVFGPFVNGVTAPCPYFPAPREPAVTIGNDVPVLLLQAKRDHTRYRDALAMHRALRGSRMVTVDLRGHGVYGREAEGLDPVPCADRAVNAYLGGGDLPREDVTCPTA
>NZ_CP023690.1|WP_150510062.1|2171849_2172839_+|aldo/keto-reductase
MTGLPTRELGALTVSAQGLGCMGMSHGYGASDDAQSTATIHRALDLGVTLFDTADFYGAGHNEELLGRALSGGRRERAVIATKFGFANRLGEPPLIRGDAAYVRQACDASLARLGVDHIDLYYLHRVDPSVPIEETVGAMADLVAAGKVRHLGLSEASARTVRRAHAVHPIAALQSEWSLWTRDLEAETAPVCRELGIGLVPFSPLGRGFLTGRVTSVEGLEANDVRRTQPRFADGNLERNLAVVDTLRVLAAEKGVTAGQLALAWVQHRGDDVVPIPGTRRETYLRENLAAATVELSADDLAAIDAAAPADGIAGTRYDEVSLAVVDR

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Crispr_ID: NZ_CP023690_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_2

3332373-3332711

TypeI-E

Consensus_repeat	Method
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	PILER-CR
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	CRISPRCasFinder
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	CRT

5 spacers

cas6e,cas5,cas7,cse2gr11,cas8e

The CRISPR arrays of NZ_CP023690_2

>merge|NZ_CP023690|2|3332373-3332711|PILER-CR,CRISPRCasFinder,CRT
GTGGTCCCCGCGCGTGCGGGGGTGGTCCCTGGTCCCACGGTGAATCCGGGACCATCTCGAAGTGGTCCCCGCGCGTGCGGGGGTGGTCCCGCCGGAACTCCGACCCCCGGAACGAAGTCGGAGTGGTCCCCGCGCGTGCGGGGGTGGTCCCGGACATCCGCGGCCCGCTTCGCCTCGCGCTCCGTGGTCCCCGCGCGTGCGGGGGTGGTCCCTCGAAGGGGCAGCAGAGCGTGGACACCGTGCTGTGGTCCCCGCGCGTGCGGGGGTGGTCCCAGCCCCTTCACCTTCACCTTCACGAAGATGATCGCCGCGTGGCCCCGCGCGTGCGAGGGTGCGCAG

>NZ_CP023690|2|1|3332373-3332645|PILER-CR
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	TGGTCCCACGGTGAATCCGGGACCATCTCGAA
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	GCCGGAACTCCGACCCCCGGAACGAAGTCGGA
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	GGACATCCGCGGCCCGCTTCGCCTCGCGCTCC
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	TCGAAGGGGCAGCAGAGCGTGGACACCGTGCT
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC

>NZ_CP023690|2|2|3332373-3332711|CRISPRCasFinder
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	TGGTCCCACGGTGAATCCGGGACCATCTCGAA
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	GCCGGAACTCCGACCCCCGGAACGAAGTCGGA
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	GGACATCCGCGGCCCGCTTCGCCTCGCGCTCC
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	TCGAAGGGGCAGCAGAGCGTGGACACCGTGCT
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	AGCCCCTTCACCTTCACCTTCACGAAGATGATCGCCG
CGTGGCCCCGCGCGTGCGAGGGTGCGCAG

>NZ_CP023690|2|1|3332373-3332711|CRT
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	TGGTCCCACGGTGAATCCGGGACCATCTCGAA
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	GCCGGAACTCCGACCCCCGGAACGAAGTCGGA
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	GGACATCCGCGGCCCGCTTCGCCTCGCGCTCC
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	TCGAAGGGGCAGCAGAGCGTGGACACCGTGCT
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	AGCCCCTTCACCTTCACCTTCACGAAGATGATCGCCG
CGTGGCCCCGCGCGTGCGAGGGTGCGCAG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_030680036.1\|3319797_3320073_-\|acyl-carrier-protein	unknown	unknown	gnl\|CDD\|223314
NZ_CP023690.1\|WP_150510889.1\|3331633_3331831_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|273953
NZ_CP023690.1\|WP_150510897.1\|3341774_3341954_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_170316296.1\|3330429_3330936_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510885.1\|3322348_3323332_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|99777
NZ_CP023690.1\|WP_150510892.1\|3334895_3335576_+\|methyltransferase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379312
NZ_CP023690.1\|WP_150510888.1\|3326241_3326532_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510893.1\|3336063_3336792_-\|type-I-E-CRISPR-associated-protein-Cas6/Cse3/CasE	cas6e	cd09727_cas6e_CAS-I-E	gnl\|CDD\|378050
NZ_CP023690.1\|WP_150510890.1\|3332797_3334105_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP023690.1\|WP_150510884.1\|3320758_3321619_-\|3-hydroxyacyl-CoA-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|224170
NZ_CP023690.1\|WP_150510895.1\|3337618_3338974_-\|type-I-E-CRISPR-associated-protein-Cas7/Cse4/CasC	cas7	pfam09344_cas7_CAS-I-E	gnl\|CDD\|378153
NZ_CP023690.1\|WP_150510886.1\|3323867_3324482_-\|flavin-reductase	unknown	unknown	gnl\|CDD\|214900
NZ_CP023690.1\|WP_150510898.1\|3342103_3345538_+\|XRE-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|379062
NZ_CP023690.1\|WP_150510896.1\|3339542_3341177_-\|type-I-E-CRISPR-associated-protein-Cse1/CasA	cas8e	pfam09481_cas8e_CAS-I-E	gnl\|CDD\|378189
NZ_CP023690.1\|WP_150510894.1\|3336773_3337622_-\|type-I-E-CRISPR-associated-protein-Cas5/CasD	cas5	cd09645_cas5_CAS-I-E	gnl\|CDD\|378243
NZ_CP023690.1\|WP_150510891.1\|3334297_3334738_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226728
NZ_CP023690.1\|WP_150515478.1\|3327131_3330353_+\|RHS-repeat-associated-core-domain-containing-protein	unknown	unknown	gnl\|CDD\|274730
NZ_CP023690.1\|WP_150510883.1\|3320087_3320759_-\|class-I-SAM-dependent-methyltransferase	unknown	unknown	gnl\|CDD\|366722
NZ_CP023690.1\|WP_150510887.1\|3324781_3326242_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|349447
NZ_CP023690.1\|WP_150515479.1\|3338970_3339534_-\|type-I-E-CRISPR-associated-protein-Cse2/CasB	cse2gr11	cd09670_cse2gr11_CAS-I-E	gnl\|CDD\|378191

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_030680036.1\|3319797_3320073_-\|acyl-carrier-protein	gnl\|CDD\|223314	COG0236, AcpP, Acyl carrier protein [Lipid metabolism / Secondary metabolites biosynthesis, transport, and catabolism].	0.000614872
NZ_CP023690.1\|WP_150510889.1\|3331633_3331831_+\|hypothetical-protein	gnl\|CDD\|273953	TIGR02072, Malonyl-_O-methyltransferase, malonyl-acyl carrier protein O-methyltransferase BioC. This enzyme, which is found in biotin biosynthetic gene clusters in proteobacteria, firmicutes, green-sulfur bacteria, fusobacterium and bacteroides, carries out an enzymatic step prior to the formation of pimeloyl-CoA, namely O-methylation of the malonyl group preferentially while on acyl carrier protein. The enzyme is recognizable as a methyltransferase by homology. [Biosynthesis of cofactors, prosthetic groups, and carriers, Biotin].	1.04749e-05
NZ_CP023690.1\|WP_150510898.1\|3342103_3345538_+\|XRE-family-transcriptional-regulator	gnl\|CDD\|379062	pfam13191, AAA_16, AAA ATPase domain. This family of domains contain a P-loop motif that is characteristic of the AAA superfamily.	0.00139097
NZ_CP023690.1\|WP_150510885.1\|3322348_3323332_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|99777	cd06170, LuxR_C_like, C-terminal DNA-binding domain of LuxR-like proteins. This domain contains a helix-turn-helix motif and binds DNA. Proteins belonging to this group are response regulators; some act as transcriptional activators, others as transcriptional repressors. Many are active as homodimers. Many are two domain proteins in which the DNA binding property of the C-terminal DNA binding domain is modulated by modifications of the N-terminal domain. For example in the case of Lux R which participates in the regulation of gene expression in response to fluctuations in cell-population density (quorum-sensing), a signaling molecule, the pheromone Acyl HSL (N-acyl derivatives of homoserine lactone), binds to the N-terminal domain and leads to LuxR dimerization. For others phophorylation of the N-terminal domain leads to multimerization, for example Escherichia coli NarL and Sinorhizobium melilot FixJ. NarL controls gene expression of many respiratory-related operons when environmental nitrate or nitrite is present under anerobic conditions. FixJ is involved in the transcriptional activation of nitrogen fixation genes. The group also includes small proteins which lack an N-terminal signaling domain, such as Bacillus subtilis GerE. GerE is dimeric and acts in conjunction with sigmaK as an activator or a repressor modulating the expression of various genes in particular those encoding the spore-coat. These LuxR family regulators may share a similar organization of their target binding sites. For example the LuxR dimer binds the lux box, a 20bp inverted repeat, GerE dimers bind two 12bp consensus sequences in inverted orientation having the central four bases overlap, and the NarL dimer binds two 7bp inverted repeats separated by 2 bp.	5.47246e-08
NZ_CP023690.1\|WP_150510890.1\|3332797_3334105_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	1.16119e-06
NZ_CP023690.1\|WP_150510892.1\|3334895_3335576_+\|methyltransferase-domain-containing-protein	gnl\|CDD\|379312	pfam13649, Methyltransf_25, Methyltransferase domain. This family appears to be a methyltransferase domain.	7.64017e-18
NZ_CP023690.1\|WP_150510893.1\|3336063_3336792_-\|type-I-E-CRISPR-associated-protein-Cas6/Cse3/CasE	gnl\|CDD\|378050	pfam08798, CRISPR_assoc, CRISPR associated protein. This domain forms an anti-parallel beta strand structure with flanking alpha helical regions.	1.12019e-37
NZ_CP023690.1\|WP_150510884.1\|3320758_3321619_-\|3-hydroxyacyl-CoA-dehydrogenase-family-protein	gnl\|CDD\|224170	COG1250, FadB, 3-hydroxyacyl-CoA dehydrogenase [Lipid metabolism].	8.32663e-79
NZ_CP023690.1\|WP_150510895.1\|3337618_3338974_-\|type-I-E-CRISPR-associated-protein-Cas7/Cse4/CasC	gnl\|CDD\|378153	pfam09344, Cas_CT1975, CT1975-like protein. 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 family is represented by CT1975 of Chlorobium tepidum.	2.34463e-53
NZ_CP023690.1\|WP_150510886.1\|3323867_3324482_-\|flavin-reductase	gnl\|CDD\|214900	smart00903, Flavin_Reduct, Flavin reductase like domain. This entry represents the FMN-binding domain found in NAD(P)H-flavin oxidoreductases (flavin reductases), a class of enzymes capable of producing reduced flavin for bacterial bioluminescence and other biological processes. This domain is also found in various other oxidoreductase and monooxygenase enzymes... This domain consists of a beta-barrel with Greek key topology, and is related to the ferredoxin reductase-like FAD-binding domain. The flavin reductases have a different dimerisation mode than that found in the PNP oxidase-like family, which also carries an FMN-binding domain with a similar topology.	3.1467e-51
NZ_CP023690.1\|WP_150510896.1\|3339542_3341177_-\|type-I-E-CRISPR-associated-protein-Cse1/CasA	gnl\|CDD\|378189	pfam09481, CRISPR_Cse1, CRISPR-associated protein Cse1 (CRISPR_cse1). Clusters of short DNA repeats with non-homologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This entry, represented by CT1972 from Chlorobaculum tepidum, is found in the CRISPR/Cas subtype Ecoli regions of many bacteria (most of which are mesophiles), and not in Archaea. It is designated Cse1.	1.82348e-49
NZ_CP023690.1\|WP_150510894.1\|3336773_3337622_-\|type-I-E-CRISPR-associated-protein-Cas5/CasD	gnl\|CDD\|378243	pfam09704, Cas_Cas5d, CRISPR-associated protein (Cas_Cas5). CRISPR is a term for Clustered, Regularly Interspaced Short Palindromic Repeats. A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This small Cas family is represented by CT1134 of Chlorobium tepidum.	1.66628e-30
NZ_CP023690.1\|WP_150510891.1\|3334297_3334738_+\|hypothetical-protein	gnl\|CDD\|226728	COG4278, COG4278, Uncharacterized conserved protein [Function unknown].	0.00331154
NZ_CP023690.1\|WP_150515478.1\|3327131_3330353_+\|RHS-repeat-associated-core-domain-containing-protein	gnl\|CDD\|274730	TIGR03696, tRNA_nuclease_WapA, RHS repeat-associated core domain. This model represents a conserved unique core sequence shared by large numbers of proteins. It is occasional in the Archaea Methanosarcina barkeri) but common in bacteria and eukaryotes. Most fall into two large classes. One class consists of long proteins in which two classes of repeats are abundant: an FG-GAP repeat (pfam01839) class, and an RHS repeat (pfam05593) or YD repeat (TIGR01643). This class includes secreted bacterial insecticidal toxins and intercellular signalling proteins such as the teneurins in animals. The other class consists of uncharacterized proteins shorter than 400 amino acids, where this core domain of about 75 amino acids tends to occur in the N-terminal half. Over twenty such proteins are found in Pseudomonas putida alone; little sequence similarity or repeat structure is found among these proteins outside the region modeled by this domain.	9.93543e-26
NZ_CP023690.1\|WP_150510883.1\|3320087_3320759_-\|class-I-SAM-dependent-methyltransferase	gnl\|CDD\|366722	pfam01596, Methyltransf_3, O-methyltransferase. Members of this family are O-methyltransferases. The family includes catechol o-methyltransferase, caffeoyl-CoA O-methyltransferase and a family of bacterial O-methyltransferases that may be involved in antibiotic production.	2.902e-69
NZ_CP023690.1\|WP_150510887.1\|3324781_3326242_-\|hypothetical-protein	gnl\|CDD\|349447	cd06228, M14-like, Peptidase M14-like domain; uncharacterized subfamily. A functionally uncharacterized subgroup of the M14 family of metallocarboxypeptidases (MCPs). The M14 family are zinc-binding carboxypeptidases (CPs) which hydrolyze single, C-terminal amino acids from polypeptide chains, and have a recognition site for the free C-terminal carboxyl group, which is a key determinant of specificity. Two major subfamilies of the M14 family, defined based on sequence and structural homology, are the A/B and N/E subfamilies. Enzymes belonging to the A/B subfamily are normally synthesized as inactive precursors containing preceding signal peptide, followed by an N-terminal pro-region linked to the enzyme; these proenzymes are called procarboxypeptidases. The A/B enzymes can be further divided based on their substrate specificity; Carboxypeptidase A-like (CPA-like) enzymes favor hydrophobic residues while carboxypeptidase B-like (CPB-like) enzymes only cleave the basic residues lysine or arginine. The A forms have slightly different specificities, with Carboxypeptidase A1 (CPA1) preferring aliphatic and small aromatic residues, and CPA2 preferring the bulky aromatic side chains. Enzymes belonging to the N/E subfamily enzymes are not produced as inactive precursors and instead rely on their substrate specificity and subcellular compartmentalization to prevent inappropriate cleavages. They contain an extra C-terminal transthyretin-like domain, thought to be involved in folding or formation of oligomers. MCPs can also be classified based on their involvement in specific physiological processes; the pancreatic MCPs participate only in alimentary digestion and include carboxypeptidase A and B (A/B subfamily), while others, namely regulatory MCPs or the N/E subfamily, are involved in more selective reactions, mainly in non-digestive tissues and fluids, acting on blood coagulation/fibrinolysis, inflammation and local anaphylaxis, pro-hormone and neuropeptide processing, cellular response and others. Another MCP subfamily, is that of succinylglutamate desuccinylase /aspartoacylase, which hydrolyzes N-acetyl-L-aspartate (NAA), and deficiency in which is the established cause of Canavan disease. Another subfamily (referred to as subfamily C) includes an exceptional type of activity in the MCP family, that of dipeptidyl-peptidase activity of gamma-glutamyl-(L)-meso-diaminopimelate peptidase I which is involved in bacterial cell wall metabolism.	4.62842e-93
NZ_CP023690.1\|WP_150515479.1\|3338970_3339534_-\|type-I-E-CRISPR-associated-protein-Cse2/CasB	gnl\|CDD\|378191	pfam09485, CRISPR_Cse2, CRISPR-associated protein Cse2 (CRISPR_cse2). Clusters of short DNA repeats with non-homologous spacers, which are found at regular intervals in the genomes of phylogenetically distinct prokaryotic species, comprise a family with recognisable features. This family is known as CRISPR (short for Clustered, Regularly Interspaced Short Palindromic Repeats). A number of protein families appear only in association with these repeats and are designated Cas (CRISPR-Associated) proteins. This family of proteins, represented by CT1973 from Chlorobaculum tepidum, is encoded by genes found in the CRISPR/Cas subtype Ecoli regions of many bacteria (most of which are mesophiles), and not in Archaea. It is designated Cse2.	2.04913e-12

>NZ_CP023690.1|WP_150510889.1|3331633_3331831_+|hypothetical-protein
MGGAVWFTDPDRLLPLIARRLAPGGVLAFAHAEPTGETYGPQSLRGPCGPNPGTSSPPYRSRACQ
>NZ_CP023690.1|WP_170316296.1|3330429_3330936_+|hypothetical-protein
MNPAVKGIAIGSARLSMLVAAIAVISTPWVAGWALSTSVIWDASFVALVYAVNLSLSRTAARWDIRKQVPQGEQVRIVVAVRRRVGKLPFPLLSDEFALALTDQRLLIQSRSTFTGRPRGALHLAEQVTLRQGKVLSIETESGVSIDALVQVAHRRDIAHWIGRRQDL
>NZ_CP023690.1|WP_150515478.1|3327131_3330353_+|RHS-repeat-associated-core-domain-containing-protein
MPPVKVGETKAPDSVREREPSPEVAAWRAAQKERARTATGKRERGAKAVAAVVPKGQGDVPWHQISDVRVTDSLVARINYSTGNLMLAGTDFEVAGAGQSLQLTRTYNSLDAPWGKVSQRWWQNYERYLQIEDSQVVLYDATGGAVTFTKRTDGTYSTPKGYRLDLKKSSNGEYTVTERGSGGKDTYSASGTLVKVTDRNGGHILVEQHDQGSEHKGFKLTESRSGRFVDLVKTDASQWQAKDNSGRTAVFDLNAAGDLAKTTDTEGKATQFGYDTSRRLTKITTPEGRVTVFTYDGDNRVTSMKRATHFDGSGETGPTYTYGYTAGEGRAGTTKVTDPAGNTTTYAHAADGEITKVTDALGRSRERTYDANLNVETAVDAMGVGSTPGNVTAYGWDTRSNPTSAKLPTGATSTLTGYKTIAGADVPGRITSADGVAVTYDYDDAGNTTKETVAGAQGGTRSFTYNPADPTCGGFKGQRCEVTDANGKTTKVTYDAKGNLSKVTPPSPLGVSTYTYDSLGRAETSVDGRGIKTVYVYDNRDRIKKVSSTNMTVTYDYDGDGNLKQRSDATGITKYDFDPLSRETIRTLQDGSQTVLTYYAEGNVESYTDPSGTVKYTYSKVNKLESLTDAQGKKTGYEYDANDFRTRTSFPGGTVETITPDKANRAQRIKATSPSGTLVDLAYDYAYTSGGTTKDGMRIRTETDTVAGLKRAYTYDSAGRLTFTVETKGTTVNDSWLYCYDKAGNLTSQGTKAGCPGGTTYTYNDASQITGRNGDTSGWSYDKAGNETAAAPTSESARTGGQWNDFSQLTSLTQGGQDFKGRYASTDQSERTQFGGTTFHNGPVGLSSKTAAGVDMSFVREPSGNLNSLRTEATSRTQSTYYYLTDAIGSTRAVVNDQGAKVNTYDYSPRGVTRNISEKVPQPYRFAGGYQDPTGLYHNEARYMDPRTGRFTQPDPAGLETNPYLYASGDPTNMIDPNGLWGMPGWAKAAVSTAVGVAVGAAATVAVGAACGATAGAACLFAGAVTGALWGGAAGAGMAKATGQNTVEGLSGGITGGLLGPWAPGLRPIYYVN
>NZ_CP023690.1|WP_150510888.1|3326241_3326532_-|hypothetical-protein
MSGPSERPAVRFDATVHPGAANRDLRGVADLDLDRIPGPEGAVRVLVSADDCRRLLESGYEVRLRALVPVRPLDSELVEGDDAVRAWLAERLQGGA
>NZ_CP023690.1|WP_150510887.1|3324781_3326242_-|hypothetical-protein
MYRTVAQLDLVGSQLATSFPQVCARTQLPELSLQGRPVFALRLRGGPGGNRRGVLLVGGTHARELMNPDALVELAVDLVTSYVNGTAVVYGGRTWTALDVKLILESLDVWIVPCVNPDGRHRVMTVDNMWRGNLRDNPGTPCDGVDLNRNAAFVWGVTEGQTSCSPCSGVFVGSGAFSEPETRNVKHLLDTRHIHSFADVHSFSELVLYPWGHAHSQTDDPGQRFTSLPTGTCAPIGVPGYREYITPRDLLRFTTVAGRVVEAIAAVRGRAYTPQTGRALYATTGTQSDYAYSRHIADPALHKTYGFTIETGPRVETVEDSFHPRDPTLIKRDAKAGVLALAQQSVCAFDLIGVRLLGRQTEVDALRRVRDEQLATTGAGREWIALVERVELPVASLVLDDERLAGRAAALIERAGKLVADAKLVVSDQDVDQGLALLSELAERAGADDEQVRVDLKAVGVALDRARGVSAAEVVRDLMSRGPLEK
>NZ_CP023690.1|WP_150510886.1|3323867_3324482_-|flavin-reductase
MVAPFDAKEFRRALGYLPTGVTVITTTGEFGEPVGMACNSFMSVSLNPPLVMICAGNESATLVDLRRSGGFCVNILGSDQGDLCRQFAMKDIDRFAGVPWTDSAAGPELSEAIAWMSCSIEVEHNAGDHVIIIAEVTALRVNPDEPTPLVFHRGKFGSFREAVEPLAAPAARPRQAVGGGHRAAPVAPGAYGYARGYAYGYAHR
>NZ_CP023690.1|WP_150510885.1|3322348_3323332_-|helix-turn-helix-transcriptional-regulator
MFPKPVAGVFEVYEWSLDRDGFAVDDIAHELGFHPAQSEEIVAKLLELQLVQPSRDRDAWFIPTDPGIASSQLLNQGELDLLERKLAVGQLRNDLARLSLLFRSSKFGSQYTNSFDIVKVPETVRLLLSEAAANSSQEVVCMQPGSGWPADDLVEAQTQDFQMLQRGVRLRVLYQHAARFDTPTREHAGKLIESGAEIRTAGALFGKIVIFDRTAAYIPASGEDGGAVVVQERSLIDFLHSCFEHVWATAKEFDTRRAEIDVIGGDMKKEIVKMLISGAKDEAIARRLGVSVRTCRKHIGQVMQMFGATSRFQFGYLVKEANLEEDV
>NZ_CP023690.1|WP_150510884.1|3320758_3321619_-|3-hydroxyacyl-CoA-dehydrogenase-family-protein
MTGNGGEQRLAVFGAGVMGIGIATLAIGRGVPVTLVDVDQARLGTARRRIRDELRLAQMMGALPRSGPTGELQFAESVAAAADATWVIEAITEVAELKTKVHREIAAAVAPGTLRVTNTSSIPVDELAGQVPAPEELAGIHFMNPPYLIGTLEVVRGPRTSERTMTAVQELLAVLGRKGIVVGDGPGFVTSRVLHRMINDAANVVEEGRATAEDVDALMEGCLGHPTGPLRTADLIGIDNLVDSLWVLHERTGDEGCRPSELLLRKVAEGNHGRKTGRGFYEYEVR
>NZ_CP023690.1|WP_150510883.1|3320087_3320759_-|class-I-SAM-dependent-methyltransferase
MAGQVQLDEGVLDYVRSVSLRDDEILRDLVNETAFMPSLNAMVTMPEEGQLLALLVGLTGASRVLEIGTFTGYSTLCMARALPPGGRIVTCDISERWTKIARRYWERAGVGDRIELRLGDGAETMAALLAEHGPETFDLVFVDADKTGYARYYEEALTQLRPGGLVVLDNTLYFGRVADPEAHDADTEAIRALNAALHVDSRVELSLLPMADGITLARKNKAQ
>NZ_CP023690.1|WP_030680036.1|3319797_3320073_-|acyl-carrier-protein
MTDSTTELPVAAIEQQIGAFLEAKTKMTWEPEVDLFASGAVSSLFAMELVVFVESTFDVEVEGPDLALDNFRTLRTMSALVTRLRVGGTGA
>NZ_CP023690.1|WP_150510890.1|3332797_3334105_-|helix-turn-helix-domain-containing-protein
MAATGTDPLWNSALVRTLVARCDPGGLIRLGRAHRGWRQSDLGARIGCSASTVSRIEQRGRRTDLTVLRRAAREVGIPTHVLAASLGLSASPATRVARDRPRCAEEADPMRRRTLLAAAGFVGPAALLSSLDDALAVTPDPTGSPVPLDARLAAARATFDAGRHTAFLQSLPGLLGDLHQDVRTRGTDHAHARLSACYGLATAALIKIGRYPQARLTADRAISHAELSGSPLAAAAAARELSIVLRHQDQSPAAQRLVHQALRGVERTGLRTDAQTSAYAQMFCTTAYTAARADDRDQALVMITEARRAARSLPDESPAERLFPLTPAAVDLYAVGVHWALGDAGTALDVGRGLHPGHFRTPERKARLHTDLGRAWWQWGKPEQTATELLSAARVSPGEVRDRLAIRTIISDLRTKHPRTPGVRELAAAAGLTAT
>NZ_CP023690.1|WP_150510891.1|3334297_3334738_+|hypothetical-protein
MVTAVKTLVRDPRTYVKPEVWEREVQLLMRDHPFDEVMATRLFHAAVSYLITAMEKWDQGLEMCCGRIVDIAVHVFILDTQNYREFCAEHFDGRFLEHIPEIAFKYDGSVERTARIIADNGFEVDRKLWEADFAKCGPCRPGSNCH
>NZ_CP023690.1|WP_150510892.1|3334895_3335576_+|methyltransferase-domain-containing-protein
MPRAPQTPAEYWDTYKPHRDEGPALRPDAAVFEWTQYPGHGPGAEFLGTPLPRRALDLGPAEGAEAAHLARQGVEVTGVDLSAVQVERARTWWQDTPRLDFVHADAVNYLTTTSTTFDAVYSVWGAVWFTDPDQLLPLIARCLAPGGVLAFAHAEPTGETYGPQRMRGKWLEGRERELTVLRWQYGPEAWTDLLKRHGFTDVDATVLPAPADEPVGTLLARAHASS
>NZ_CP023690.1|WP_150510893.1|3336063_3336792_-|type-I-E-CRISPR-associated-protein-Cas6/Cse3/CasE
MGRHSVNDSSRATITPGRFVASHSVLTLDARHPYVAKSLVDAQDMHRTVMSGFQGWGVAEGSRDARAQMGVLSTWTLDLKEAALVLVVQSRVPADWGHVPRAALRDEPYLITVDRTFRVGDAVVFRTVVNPTYNKPQDGPDGRMVRGKRVAHTKPDGVRKWLRRHFGDGREPGRVGVTTDPDDVAVHMLPPVSSPSPHKRLRIARAELRGSLTVTNPGAFVTALSDGIGHARAYSCGLLLTR
>NZ_CP023690.1|WP_150510894.1|3336773_3337622_-|type-I-E-CRISPR-associated-protein-Cas5/CasD
MTHVLLIRLAAPLQSWGTISRFAARRDSHSRPTKSAVIGLCAAALGLPRDEDLGELAQTVFGVRADHPGTPVRDYHTVGAGRYPLRPRDLITDHRRAAAASTSLDAATGDRFGHHRLADWYGAPKKIASDPVSGVLVSGELARTALITERWYLADATFLVGLQHQDLALLEGVAKALERPRRLLWLGRKSCPPSGTLTAGIEGGDLEEAFRAKQLLPGPDGTADPARRPWAWFQVPASTRGATPVQDQPVSFDASRPEHTTRWEIRRRVTIAPNATGWDVIP
>NZ_CP023690.1|WP_150510895.1|3337618_3338974_-|type-I-E-CRISPR-associated-protein-Cas7/Cse4/CasC
MTDASAPRGQFLSLHLLETLVAVLPVRDENGSPKTLVYGGVERHLITSQARRRAERVHARNRANDGVGPLAGRTTGLRTREWALITAWALESAHGWDRDEAVAMARAVLEATGLKFGDPAKKTVANLTKVLVFAPADTGDRIAAHIAAHAGELCGWRDAYLGAQAAAAKPRRGGRKTAEEPEGDDGTAADSAADGKVPPLPKASRDAVLTALAPRDAIDIALYGRFLAEIAESPNVDGAVQSAHAFTIHEAEQVDDFYAAADDAKLERKKNALDFLDAADDAGAGMTGYQSLISGTFYRHSVLDRRQLRANLQAAGMTEEEAADAAVGAEREFVTAFVEAFPEAKKNSTASTGSLPALVLAFEGERPYSYAAAFQRPVDENAVDKEEGGPAGLAGVRRLLRHHVFVSERRPDLRTARLLTYDPQIDALIDELEARHAVGGVRVETIDGLTP
>NZ_CP023690.1|WP_150515479.1|3338970_3339534_-|type-I-E-CRISPR-associated-protein-Cse2/CasB
MERDAAAASTDQSGGAQLTAWLTALVRNREYGELANLRRGRVRTNAHIRAGWYAPEQVEEREIYEQVAFLFAVYHRGVSKPAPGVGSLGTAVRRIGGSFGRGPNDPGAARLVDRIVTSRRVPWRHLQHAIARLRACEQPPPSWSRLVDDLQRWHDRKARVAYGWAVDFHEPEPHDTGRNTTQKGPST
>NZ_CP023690.1|WP_150510896.1|3339542_3341177_-|type-I-E-CRISPR-associated-protein-Cse1/CasA
MRVPDLSQPNGKCPRPRWDPRHHPCVRALSLDGEAVEQNLLQLLTRAEELTGIGGMTPGEKVALIEYLLAICYASGAYPSSTEDWTRWVLESQSLRKAAAWLAVQSDEDWDLFHPARPLGQNVRLADFMGRYGTGPAQLVIERAGDYAQFADHHHLEDPEALPAADAFRAMLTQHTFGLAGRARVSGKGTLGPALTNLAAGRLSGRIRVLALGPTLGDTLRLNLAPTADGPGALNLTWTEGPIERRGFTARPRGRAVTGFADLHSYLGRSVLMRPVPGAYGESAAVDRVLVGAGELLELDPELHLQDAVMSATRTGERKPLWPSATRDLWREAHALYAAVEEEAGGFYTRLGKLPKARQLGGHPFALHGRHPFDLLAVGLVSNKSTPVTWVTSVFPFAPGLAPVLHQASSRGSQVAEHIARSLDKAAYSAWEIAYPNPRPTDKKAQLARFDARGEHWKATEEPFHTLLQDVADGELVTDCMAEYVEWLVPMARRALEKRLDSLPGNTRGMRARAAALRRFDAEVTGFRAPDDLKGLNGLKGGEG
>NZ_CP023690.1|WP_150510897.1|3341774_3341954_-|hypothetical-protein
MLLLPDLLTASAALGVATGATYATTLLTVVLVSVVSRNPTRRRDARATLTILVRRRPPR
>NZ_CP023690.1|WP_150510898.1|3342103_3345538_+|XRE-family-transcriptional-regulator
MSGQGGDTVSREATKKLGTQLKELYQAVRTDHRNVTYVMLAERFGISRSAVGAWMTGRYPPDGELVTKYLAVVAYLESKSPDKPLPPGVWRRAIKKAQDEGVRNQGKRPPRSGPPAVRPFRYPHTAPQRVARDLIGRDAELDALAELSRRGPSYSALYGPPWAGKTALLAAFVTGHVPSEVDVISYFVQWSSSTNEAQKFLQTMVAQLDLLVGNKRSVPGDEASLFALYEQAVQTSSERGRSLLLVVDGLDEDAAAQPGQQSIASLLPKRPPPGLRVLVSSRWHPPLPANLDGDHPLQSAAIIPGFRPSPIGHSLRGAASEDLRALLECPDGREVIGLLALARGGLSYRSLIELMELGERAKPPAPVDLERMLRNVAGRGVAPEDLEPDTYVLAHEELYRTATQLLEGRTTTDLTQRLHHWADDYRNKQWPPTTPLYLLNGYPELLRGTGDTARFTTFALDHRRLLRLADHARTDLALASLDHVTRMSQGLDALASAAASRFFLERERRPVPRDVLRALARAGDTAWARSLALSPRDPASKATRLIAVTQALVETARPGATDIAREAANWAQRARYQDALLAPAEEPDTEGIVAQVTVVLASAGAPDEAIRLLDTIDVCSPGNFASTSDAAGRLLDSHPAFATRLLDELCDEADHLAYEADEGSAVAVEMWAAVAAADPGRTDPVHHRMAEFGRWLDVTSAGLAAVDCPAQAASVLAKTRPDDARALVDAALRRMDGLLNAPAGDRARETLARLVRALLDVDGKPDRARALLDGAPPEATARARMTLADEPDEPNELLARMRHLADIGDGPRARLVLAQATRQAGGTAAGANPIPWLPLLAGALAHHGTPWLTEAHTLLARASDPCLSLPVRILTSASLAHADAGRSGQALRYAEEAEDVVGDVDFTDPRAPLVRGLVAQAFAHAGQAQQAARWSAPDAGRRSGRARRHDRRVALAVEVGLAPEAIVPGVERPGLKSGYCTRLAHAVLRIAAGKRAEADLVALEDEARARGATEPLLSTGLALLHTVLGAPDRALRAAARLTDPVERATALTTVAAHLAGVPAHLDVAATTGDAWAISLLRVLARQAVPGHAGDDTTVRDVLRDVLSTSGWYEALPVLARTAPEAVSAVADVLAQHRQARQGEP

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Crispr_ID: NZ_CP023690_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_3

3354954-3355038

TypeI-E

Consensus_repeat	Method
CATGACGAGATTGGTGAGATTGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_3

>merge|NZ_CP023690|3|3354954-3355038|CRISPRCasFinder
CCTGACGAACATGACGAGATTGGTGAGATTGGCTCCGACCTGCGGTTTCTTGCGCACCTGTCACTGACGAGATTGGTGAGATTGG

>NZ_CP023690|3|3|3354954-3355038|CRISPRCasFinder
CCTGACGAACATGACGAGATTGG	TGAGATTGGCTCCGACCTGCGGTTTCTTGCGCACCTGTC
ACTGACGAGATTGGTGAGATTGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150510909.1\|3352562_3352841_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510905.1\|3350578_3351028_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510908.1\|3351843_3352566_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510906.1\|3351024_3351492_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510904.1\|3350324_3350582_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510916.1\|3357491_3357734_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510915.1\|3356826_3357450_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_170316419.1\|3357830_3357992_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510907.1\|3351652_3351847_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510917.1\|3358185_3358914_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510913.1\|3355817_3356207_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_170316416.1\|3349753_3349996_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP023690.1\|WP_150510914.1\|3356307_3356799_+\|single-stranded-DNA-binding-protein	unknown	unknown	gnl\|CDD\|236092
NZ_CP023690.1\|WP_150510903.1\|3349992_3350307_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|378935
NZ_CP023690.1\|WP_150510910.1\|3352931_3353792_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235927
NZ_CP023690.1\|WP_150510919.1\|3359155_3360265_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_170316417.1\|3351488_3351656_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510912.1\|3355605_3355821_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150510918.1\|3358913_3359159_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_170316420.1\|3358012_3358189_+\|hypothetical-protein	unknown	unknown	unknown

>NZ_CP023690.1|WP_150510910.1|3352931_3353792_+|hypothetical-protein
MNDTIAYNRLADLLRDMGEPTRYQGGALRTRGLCHDGDAPGTVAIRPGNNGSVVIHCHKCGGNAGFLAAIGWSETDLFDTPLERQRDRPADDTWIPCRDRDHKRVAQYVYRDENSAVVHGVTRCDHKCFAQWRPSHETKTGRRWSLNDKEGNRLVRTVPYRLPELLKAKEADRVIWIAEGEKDVHALGDHGLPATCNAGGSGKWTAEHARHLEGADVTIVADRDAKGREHATVVVETLRGLARSVYVVQARTGKDAADHFAAGHKDAQFVQVWAPVPHPSDPAVAA
>NZ_CP023690.1|WP_150510909.1|3352562_3352841_+|hypothetical-protein
MTDRRPGQWPVEQPANLDKIEKGYSLTSTPGEDELYMQRAAERALHEMVMDSIRHDLQQQPSTLSVLSAARHWCERITATADEIARTKRRTA
>NZ_CP023690.1|WP_150510908.1|3351843_3352566_+|hypothetical-protein
MTATFRKLAEQVVARHDDHLLDYGPDKQADRVVAALQRLNRIVDLTPAIGTDIDLAGFGKVPAQYASGNDSYFLLSDASEQLGWFHPRACKWAEKRFAWAVQEQRRIDEERGDGRLGWECLTGHVDLELHLCVDDPQAKPDAGGRRWSDSGDWLISTDRIPDLLASSPWGKEFMDNSMDAFRHAAREIFGDKLKQSPVIGPDGQPTGSNAYDLFEPQLPKDEALRRARRGPALDDEEGLS
>NZ_CP023690.1|WP_150510907.1|3351652_3351847_+|hypothetical-protein
MNDDKPRPDCTHWIGTEHRHCREGDGVRQYLTGPRCPAHTPAALASRPEPQPGPGWPIHRQEAT
>NZ_CP023690.1|WP_170316417.1|3351488_3351656_+|hypothetical-protein
MSAPSARPVRFEDPARNTAYWQRSTRIVDAAPPLTDAQRAIIRTAFHQPTERRAA
>NZ_CP023690.1|WP_150510906.1|3351024_3351492_+|hypothetical-protein
MSDNTQIPERVMSVTNFLNEDSPLTAAQRTLTLDTGLAAHRTTPIETALRDIDCESEHADLPWLSAEIVVLDDKPQAYGRTTNVWLAYGAAVTEMLPVQGREALAAMREFADRYEALLDLADEIAKGDFEGDPEITRLDQEAMDRHIRAVNEGRA
>NZ_CP023690.1|WP_150510905.1|3350578_3351028_+|hypothetical-protein
MTVMDNTRPRTWEFTDVDTGQTRTITCTPWCNISHASDIAHPCLPSEISCISYDRANTAALPVACGHDAEDVYVMSALIEVDHFDPDPARRAPHAIVEIVQDHFTGALDPDGLQALIGLFEQRVAALRIRHAELVTARAEHQPQKEAQA
>NZ_CP023690.1|WP_150510904.1|3350324_3350582_+|hypothetical-protein
MSTVSETATAPSTLPEQSIRITLAVEIMIDLDTGRPMLLASTDANEGDIHEVTPDEFLALAHQARAEIDRMARLALTHARQAVRS
>NZ_CP023690.1|WP_150510903.1|3349992_3350307_+|helix-turn-helix-domain-containing-protein
MTRALTVDEVLALPAMPNAWPDGAGACGGISRTTWYSLISSNQTPVPVIRVGRCLKVRRSDLLNFLGIKESAAEVESATGTEENDDAPGVEPGAPIEQSAPTAK
>NZ_CP023690.1|WP_170316416.1|3349753_3349996_+|helix-turn-helix-domain-containing-protein
MSSYQLRSDSLLKAASARGDRSCYAISKRTGIAESTLSRLRRGVARPATETLLILAAAYGLSIDDLIDQGADDQSEEGAA
>NZ_CP023690.1|WP_150510912.1|3355605_3355821_+|hypothetical-protein
MNVDDVIAERIAAARRRIEAAKKRRAALNASRQRGLAIRHAAKLRNQAGARAANGTAGVTPTPANSTEENQ
>NZ_CP023690.1|WP_150510913.1|3355817_3356207_+|hypothetical-protein
MTDIDLTTRALEPVSQFVLTTSHGDNDPHRLLAFHRTFGAAMEAYEIRYHQARHHEEQPEATAREEALYAALAAAGRPYAAAALSRAASVLGDKFNETTFLALGDTAAALDLAIVEDLNGANGTGEDDA
>NZ_CP023690.1|WP_150510914.1|3356307_3356799_+|single-stranded-DNA-binding-protein
MSGETVITVVGNLVDDPELRFTPAGAAVAKFRIASTPRRFNKTTNAWEDGDALFLTCSVWRQAAENAAESLTRGMRVIVQGRLKQRSYEDREGVKRTVYELDVDDVGPSLARATAKVTKNPAGGGHPAADPNGSPDPWASARPANGQQQPAGQSAGYSDEPPF
>NZ_CP023690.1|WP_150510915.1|3356826_3357450_+|hypothetical-protein
MNACGLCERPSEHSYLCPGCARGLAESLDQLPVLHDELVECLVPRRYGFGDIVATRGAAGPRSPLDEDVLDEMNSGHMAAVVHLWRVDVQRVRWPSHGEPPPAGLAADCRWLAMELNWIAAEYVAAGDLAREVSDLERDARSIVGDPAPRPQRLGTCVAVDTGGVVCGAVIKRMPGQTRLRCRWCGYTYETAQDWMRLQHFQPEEVA
>NZ_CP023690.1|WP_150510916.1|3357491_3357734_+|hypothetical-protein
MEPQPWRERIRDEDKLLEQLNQLASQAADRRAQALLDGVDELGTIADVARDLGKSWTAVDKAIKKYESKKASTTDAPTTE
>NZ_CP023690.1|WP_170316419.1|3357830_3357992_+|hypothetical-protein
MTDHVAGRSVPASSLPSRRLVAAGIIRRTPGRTLTVRATPAGVTGIIRKAVTR
>NZ_CP023690.1|WP_170316420.1|3358012_3358189_+|hypothetical-protein
MDNPTPPSTLTTAVHVAQQMLGAYGSSSRDGFDYAEAYGALRESLRILLRAVEAGENA
>NZ_CP023690.1|WP_150510917.1|3358185_3358914_+|hypothetical-protein
MRYPHLPAYGPTEAHADEDARPDVVVRVAYALDREQLLAALSIGFTELDPDRAPEDLTVDEVRREVEGWLAAQGIIELERYVIQGQLTAYPPKQQAVMDALAAALVRAYPPPPAEEPDTGPRYGDGTVNVHTRDAGRITLREPRWCIGEHRGGEYRVDVHHMGATQHTRFHTPMGPAYVALSAAQSPLSSQPQPELHAEVSGSWSMTCDTHVARAADALEEMAAHLRGQQALLAQLEDGGPR
>NZ_CP023690.1|WP_150510918.1|3358913_3359159_+|hypothetical-protein
MLKKTRARRAAAVRHRQLLDTAERVVRRHILEGQSGSDATPAEMVALAFGRLALHIDEDEARDYLNAVLVERGYPLPGGAQ
>NZ_CP023690.1|WP_150510919.1|3359155_3360265_+|hypothetical-protein
MSTRELTRPQKGMLAAAAVPMLAVGGFGAWGTYTNVVTEFHRAATAMGVVAAGEGLTLVLALTMLALTLLGQATPRPVHIGLWLAPVAASGVGISIADTVTEAVVYAATPLAMSGAAEGLGLIARRIVIYTTGIDAEARRRIADTVQRLAYEQAVAERHPDEDKREAALRKSWKLAQDIGRDDPELAEGLVAVQRERLRQGADGALAGMLTAAPAPKQVGPARQETAEEVLRRKLATMGAEDAVRLVRDAHPDAPLAELVEICNDHGVHVTPVQVAVILDQRPEQHTVYRQDAPDAPLVSGLPLVTVEGAVVEAASFLGPDAKARQISEHLARHRRLVVAEPYIRTALSREAKRQQGQAPAKPMEGGYA

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Crispr_ID: NZ_CP023690_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_4

3690251-3690352

Orphan

Consensus_repeat	Method
CCGGCCGCGCCCCGACCTGGCGGCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_4

>merge|NZ_CP023690|4|3690251-3690352|CRISPRCasFinder
CCGGCCGCGCCCCGACCTGGCGGCTGACCCGCCGTCGTCCGTTTTCTCCCACCCACCCACCCGTATCACCCCGGCGACCGGCCCCGCCCCGACCTGGCGGCT

>NZ_CP023690|4|4|3690251-3690352|CRISPRCasFinder
CCGGCCGCGCCCCGACCTGGCGGCT	GACCCGCCGTCGTCCGTTTTCTCCCACCCACCCACCCGTATCACCCCGGCGA
CCGGCCCCGCCCCGACCTGGCGGCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150511162.1\|3702098_3703307_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|225371
NZ_CP023690.1\|WP_150511149.1\|3681695_3682772_-\|trypsin-like-serine-protease	unknown	unknown	gnl\|CDD\|365866
NZ_CP023690.1\|WP_150511156.1\|3689723_3690170_+\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|240040
NZ_CP023690.1\|WP_150511163.1\|3703303_3703741_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP023690.1\|WP_150511150.1\|3683105_3684197_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150515507.1\|3696489_3697035_-\|sigma-70-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274357
NZ_CP023690.1\|WP_150511152.1\|3685593_3687348_-\|TIGR03767-family-metallophosphoesterase	unknown	unknown	gnl\|CDD\|213859
NZ_CP023690.1\|WP_150511161.1\|3701100_3701985_-\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP023690.1\|WP_150511159.1\|3699450_3700461_+\|aspartate-semialdehyde-dehydrogenase	unknown	unknown	gnl\|CDD\|237845
NZ_CP023690.1\|WP_150511151.1\|3684287_3685472_-\|serine-hydrolase	unknown	unknown	gnl\|CDD\|365903
NZ_CP023690.1\|WP_150511155.1\|3688779_3689667_+\|pyridoxamine-5'-phosphate-oxidase-family-protein	unknown	unknown	gnl\|CDD\|274926
NZ_CP023690.1\|WP_150511147.1\|3678241_3678883_-\|DsbA-family-protein	unknown	unknown	gnl\|CDD\|376526
NZ_CP023690.1\|WP_150511154.1\|3688309_3688765_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319898
NZ_CP023690.1\|WP_150511153.1\|3687597_3688152_-\|CGNR-zinc-finger-domain-containing-protein	unknown	unknown	gnl\|CDD\|378696
NZ_CP023690.1\|WP_150511148.1\|3679030_3681607_+\|aminopeptidase-N	unknown	unknown	gnl\|CDD\|274121
NZ_CP023690.1\|WP_150511157.1\|3690628_3693922_+\|S8-family-serine-peptidase	unknown	unknown	gnl\|CDD\|173796
NZ_CP023690.1\|WP_150511160.1\|3700577_3701087_+\|DUF1203-domain-containing-protein	unknown	unknown	gnl\|CDD\|377693
NZ_CP023690.1\|WP_150511158.1\|3694009_3695506_-\|M28-family-peptidase	unknown	unknown	gnl\|CDD\|349873
NZ_CP023690.1\|WP_150511164.1\|3703975_3704827_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045
NZ_CP023690.1\|WP_150515506.1\|3695665_3696391_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150511162.1\|3702098_3703307_+\|MFS-transporter	gnl\|CDD\|225371	COG2814, AraJ, Arabinose efflux permease [Carbohydrate transport and metabolism].	3.32834e-73
NZ_CP023690.1\|WP_150511149.1\|3681695_3682772_-\|trypsin-like-serine-protease	gnl\|CDD\|365866	pfam00089, Trypsin, Trypsin.	7.84919e-07
NZ_CP023690.1\|WP_150511156.1\|3689723_3690170_+\|NUDIX-domain-containing-protein	gnl\|CDD\|240040	cd04684, Nudix_Hydrolase_25, Contains a crystal structure of the Nudix hydrolase from Enterococcus faecalis, which has an unknown function. In general, members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity. They also contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	1.51176e-35
NZ_CP023690.1\|WP_150511163.1\|3703303_3703741_-\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.29482e-16
NZ_CP023690.1\|WP_150515507.1\|3696489_3697035_-\|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.	1.23522e-24
NZ_CP023690.1\|WP_150511152.1\|3685593_3687348_-\|TIGR03767-family-metallophosphoesterase	gnl\|CDD\|213859	TIGR03767, P_acnes_RR, metallophosphoesterase, PPA1498 family. This model describes a small collection of probable metallophosphoresterases, related to pfam00149 but with long inserts separating some of the shared motifs such that the homology is apparent only through multiple sequence alignment. Members of this protein family, in general, have a Sec-independent TAT (twin-arginine translocation) signal sequence, N-terminal to the region represented by this model. Members include YP_056203.1 from Propionibacterium acnes KPA171202.	0
NZ_CP023690.1\|WP_150511161.1\|3701100_3701985_-\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	2.5637e-28
NZ_CP023690.1\|WP_150511159.1\|3699450_3700461_+\|aspartate-semialdehyde-dehydrogenase	gnl\|CDD\|237845	PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.	0
NZ_CP023690.1\|WP_150511151.1\|3684287_3685472_-\|serine-hydrolase	gnl\|CDD\|365903	pfam00144, Beta-lactamase, Beta-lactamase. This family appears to be distantly related to pfam00905 and PF00768 D-alanyl-D-alanine carboxypeptidase.	5.23971e-54
NZ_CP023690.1\|WP_150511155.1\|3688779_3689667_+\|pyridoxamine-5'-phosphate-oxidase-family-protein	gnl\|CDD\|274926	TIGR04025, hypothetical_protein, PPOX class probable FMN-dependent enzyme, DR_2398 family. Members of the PPOX family (see pfam01243) may contain either FMN or F420 as cofactor. This subfamily consists of proteins mostly from species that lack the capability to synthesize F420, and therefore most likely all bind FMN.	2.40121e-16
NZ_CP023690.1\|WP_150511147.1\|3678241_3678883_-\|DsbA-family-protein	gnl\|CDD\|376526	pfam01323, DSBA, DSBA-like thioredoxin domain. This family contains a diverse set of proteins with a thioredoxin-like structure pfam00085. This family also includes 2-hydroxychromene-2-carboxylate (HCCA) isomerase enzymes catalyze one step in prokaryotic polyaromatic hydrocarbon (PAH) catabolic pathways. This family also contains members with functions other than HCCA isomerisation, such as Kappa family GSTs, whose similarity to HCCA isomerases was not previously recognized. Some members have been annotated as dioxygenases, dehydrogenases, or putative glycerol-3-phosphate transfer proteins, but are most likely HCCA isomerase enzymes.	1.47754e-05
NZ_CP023690.1\|WP_150511154.1\|3688309_3688765_+\|VOC-family-protein	gnl\|CDD\|319898	cd06587, VOC, vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC is found in a variety of structurally related metalloproteins, including the type I extradiol dioxygenases, glyoxalase I and a group of antibiotic resistance proteins. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). Type I extradiol dioxygenases catalyze the incorporation of both atoms of molecular oxygen into aromatic substrates, which results in the cleavage of aromatic rings. They are key enzymes in the degradation of aromatic compounds. Type I extradiol dioxygenases include class I and class II enzymes. Class I and II enzymes show sequence similarity; the two-domain class II enzymes evolved from a class I enzyme through gene duplication. Glyoxylase I catalyzes the glutathione-dependent inactivation of toxic methylglyoxal, requiring zinc or nickel ions for activity. The antibiotic resistance proteins in this family use a variety of mechanisms to block the function of antibiotics. Bleomycin resistance protein (BLMA) sequesters bleomycin's activity by directly binding to it. Whereas, three types of fosfomycin resistance proteins employ different mechanisms to render fosfomycin inactive by modifying the fosfomycin molecule. Although the proteins in this superfamily are functionally distinct, their structures are similar. The difference among the three dimensional structures of the three types of proteins in this superfamily is interesting from an evolutionary perspective. Both glyoxalase I and BLMA show domain swapping between subunits. However, there is no domain swapping for type 1 extradiol dioxygenases.	8.50773e-20
NZ_CP023690.1\|WP_150511153.1\|3687597_3688152_-\|CGNR-zinc-finger-domain-containing-protein	gnl\|CDD\|378696	pfam11706, zf-CGNR, CGNR zinc finger. This family consists of a C-terminal zinc finger domain. It seems likely to be DNA-binding given the conservation of many positively charged residues. The domain is named after a highly conserved motif found in many members of the family.	3.18775e-19
NZ_CP023690.1\|WP_150511148.1\|3679030_3681607_+\|aminopeptidase-N	gnl\|CDD\|274121	TIGR02412, Aminopeptidase_N, aminopeptidase N, Streptomyces lividans type. This family is a subset of the members of the zinc metallopeptidase family M1 (pfam01433), with a single member characterized in Streptomyces lividans 66 and designated aminopeptidase N. The spectrum of activity may differ somewhat from the aminopeptidase N clade of E. coli and most other Proteobacteria, well separated phylogenetically within the M1 family. The M1 family also includes leukotriene A-4 hydrolase/aminopeptidase (with a bifunctional active site).	0
NZ_CP023690.1\|WP_150511157.1\|3690628_3693922_+\|S8-family-serine-peptidase	gnl\|CDD\|173796	cd04857, Peptidases_S8_Tripeptidyl_Aminopeptidase_II, Peptidase S8 family domain in Tripeptidyl aminopeptidases_II. Tripeptidyl aminopeptidases II are member of the peptidase S8 or Subtilase family. Subtilases, or subtilisin-like serine proteases, have an Asp/His/Ser catalytic triad similar to that found in trypsin-like proteases, but do not share their three-dimensional structure (an example of convergent evolution). Tripeptidyl aminopeptidase II removes tripeptides from the free N terminus of oligopeptides as well as having endoproteolytic activity. Some tripeptidyl aminopeptidases have been shown to cleave tripeptides and small peptides, e.g. angiotensin II and glucagon, while others are believed to be involved in MHC I processing.	7.3429e-62
NZ_CP023690.1\|WP_150511160.1\|3700577_3701087_+\|DUF1203-domain-containing-protein	gnl\|CDD\|377693	pfam06718, DUF1203, Protein of unknown function (DUF1203). This family consists of several hypothetical bacterial proteins of around 155 residues in length. Family members are present in Rhizobium, Agrobacterium and Streptomyces species.	8.88529e-42
NZ_CP023690.1\|WP_150511158.1\|3694009_3695506_-\|M28-family-peptidase	gnl\|CDD\|349873	cd03876, M28_SGAP_like, M28 Zn-peptidase Streptomyces griseus aminopeptidase and similar proteins. Peptidase family M28; Streptomyces griseus Aminopeptidase (SGAP, Leucine aminopeptidase (LAP), aminopeptidase S, Mername-AA022 peptidase) subfamily. SGAP is a di-zinc exopeptidase with high preference towards large hydrophobic amino-terminal residues, with Leu being the most efficiently cleaved. It can accommodate all except Pro and Glu residues in the P1' position. It is a monomeric (30 kDa), calcium-activated and calcium-stabilized enzyme; its activation by calcium correlates with substrate specificity and it has thermal stability only in the presence of calcium. Although SGAP contains a calcium binding site, it is not conserved in many members of this subfamily. SGAP is present in the extracellular fluid of S. griseus cultures.	3.19004e-113
NZ_CP023690.1\|WP_150511164.1\|3703975_3704827_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	1.71526e-06

>NZ_CP023690.1|WP_150511156.1|3689723_3690170_+|NUDIX-domain-containing-protein
MHKELRVAAYAVCVRDGSVLLARWVAGDGSKRWTLPGGGMDHGEDPYDTVIREVDEETGYAVEPVALLGVDSLRRRYPRRLGAVADFHGLRIVYEGRVVGGDLRHETSGSTDLAAWHALDSVPGLDRVSLVDVGLGLWRGRPPNGHLT
>NZ_CP023690.1|WP_150511155.1|3688779_3689667_+|pyridoxamine-5'-phosphate-oxidase-family-protein
MTGHDPYHQGSRAVQDRVGVRALADHVGRSIGPGIRPVAAAFLELQPMLVIGARDPASGRVWASPLTGDPGFVRATGAHQMSVAGGAGAGDPLADALGRPGTPVGTIALDPRTRRRMRLGGRARPTPRGLAIEADRVFSNCPKYLQKRQLLAGRRAGGPAAEPRVSAELTAAQRRFVAAADTFFIATVRDGGADASHRGGNPGFVRVLSPTELSWPDYAGNAMFLTLGNLAADPGAGLLFLDWTTGTALQLTGTATTAYGPGGARTVHFALTEAVETSGASPWTWSAPEYSPANP
>NZ_CP023690.1|WP_150511154.1|3688309_3688765_+|VOC-family-protein
MTAISAPPTGHIGLNVTDLDRSLAFYRDVIGFEVTGEGAHEGRRYAFLGRAGTLALTLWQQASGAYDSGRAGLHHLSFEVDSVDAVREYERDLRAYGVEFAYDGVVPHGEGAASGGIFFHDPDGTRLEICTRSGAGDGAAPAGAAPTCGFF
>NZ_CP023690.1|WP_150511153.1|3687597_3688152_-|CGNR-zinc-finger-domain-containing-protein
MPAAHDPRPLTGEPLSLDLLNTRWMHDGARQDLLDDPEGLAVWLAANGLDERFTADAPTLRNVLAARDALAGLVDLPGKPGGEATAVARLDAVLTHGRIRARLTPEGPAEEPEFAEPAWGPAWLAARDYLDLLSAAPDRIRGCAHEACVLHFFDTSRNGTRRWCSMAVCGNRAKASRHYARTRP
>NZ_CP023690.1|WP_150511152.1|3685593_3687348_-|TIGR03767-family-metallophosphoesterase
MSRIRSVATAVTTAAVNRRAFLAATGAVSLSAGVGYALGPGAGHGEAAAAHRGPVAVSRRAPAAPLAPYRAGTTLGTVAAPRGTSGFRRLGDGPAWPRVVRADLAAPHRGREARRTALAAFVQFTDLHLVDVQHPLRYEYLRAQTASAWRPQEALSVAGAVSLVERVNALRGAPATGAPLHFVMTTGDNTDNNSRTELDWFLKVMSGGRVTPNSGDPRHYEGVQNSGLELYWHPDAALRDADKRLGFPRLHGFLDAAIRQVNSPGLNLPWYSTVGNHDALPGGCYAPGDSYFADLAVGGRKLMSLDEARGAALWKAVKKGRDPKGAHFKELLRAEARRMRPVTPDEARAPFTPTEYVQAHLDPAHAGRGPVGHGYTQENLANRTQYYAFRITDDVLGISLDTTDPGGHYEGSLGTAQLRWLERILKAVERGGDASYAIVFSHHTSRSMRNLTTDPHHPREQRHGGDEVLALLRRHRSVLAWVNGHSHKNAITPHGSLWEVSTASHVDFPQLARVLELVDNHDGTLSLFTTLIESAAPHRTDFADLSQTGLAALYRELALNAPGAKPALGGAPGDRNTELVLRKR
>NZ_CP023690.1|WP_150511151.1|3684287_3685472_-|serine-hydrolase
MAVPTRLTPVRTGFVGAVVAAAAVAGALTGPAAAAPRTDRDHHRTRAAIEAAVRAGVPGVTAHAHDRRGPWSAAAGVGDLRAGTPRGEHDRFRAASITKTFVATVVLQLEAEGRLDLDDKVGTWLPGVIEGNGHDGDEISVRQLLNHTSGIYDYSADPDFDRRLATPEFYAHRYRTWEPDELVAIAMRHEPDAAPGRDWNYSNTNYVVAGMIVEKVTGRPYGDEIRDRIINPLRLRATSVPGTTPTLPRPASRAYSKLSGSKLSGDATGKTYDVTELNPTMAGAAGEMISDAADLNRFYAALLRGALLPAQQLAAMKKTVLAKGEEGAGGRYGLGLLRLELPCGTVVWGHGGGIHGSLSLALTTADGRHALALNYNGDWSRGQDRILNAEFCGA
>NZ_CP023690.1|WP_150511150.1|3683105_3684197_+|hypothetical-protein
MNHNTPLSPRPLRHLTDVQRRVMSTAQLRTHGVGAAEVHAHCRPGGPWQQFLPGVYLLHPGPPTSEERLHGVLLYAGRPPAKESRAIPAQPRPGEPHAAYADAMITGLAALALHRFSSAPPLLSLDRIDVLVPRTRRLRSTGCARLVRAYTLPTPLQVTGVPVAPVPRALADAVAQLADAGAVRRLLTEAVRGGHCEPAALVKELNRARLLGRPHVVDAVDSLLAEGRAIAEDRLHALVRDHGLPDPLWNVDLRLPGGPHLGGVDAYWPEQAVAVELDTRAPRHGLRPHPRQGRTDRHQYEDDEQWSEYVRKREHLERLGITVVHITPKKLRDAADQQAAVVRTALMAAPDRDPAAYVVVLPR
>NZ_CP023690.1|WP_150511149.1|3681695_3682772_-|trypsin-like-serine-protease
MTPPRAITRRLVLTGIGVAALIAGTLTAAATSSAASDPTPKAIGATAAGRLADSLTDGSRGGTAGAYYDSAAKKLVVNVLDEAAADRVRAAGAEPRAVTHSQAQLDAVLRTLGERAVPGTSRGTDPVLNKVVVTADSTVTGAALDRLKQRVAAQGGKAVLKRTAGTFQPLIRGGDAIWSSSGRCSLGFNVVKNGQPYFLTAGHCAALAGTSWSETQGGPVIGQVEDYGFPGRDDAIVKYTANVAHPSEVNLYNGGSQQITGARQAVVGEQVQRSGSTTRLHGGTVQRLNVSVTYPQGTVNGLIQTNVCAEPGDSGGAMFAGSSALGLTSGGSGNCSSGGQTFFAPVVDALSRYGAQIG
>NZ_CP023690.1|WP_150511148.1|3679030_3681607_+|aminopeptidase-N
MPGENLSRDEAQERAALLSVDGYEVFLDLRSAVGDSQEGDTTPRTFRSVTTIRFRCAEPGAASFADLIAPSVTALSLNGKDLDPSEVFDGSRIALEDLREENELVVDAQCAYSRTGEGMHRFVDPEDGEVYLYTQYEPADSRRVFANFEQPDLKAPFRFSAQAPEGWTVWSNGAGEQADGVWKFAETKPISTYITAVVAGPYHYVTDSYERVFEDGTRLEIPLGAMCRKGLAKHFDADDVFLVTKQGLDFFHDHFDFPYPFGKYDQAFVPEYNLGAMENPGCVTFREEFIFRGKVTQASYERRANVILHEMAHMWFGDLVTMRWWDDLWLKESFADFMGSFSMVEATRFTNGWITFANNRKAWAYRADQLPSTHPVTADIRDLEDAKLNFDGITYAKGASVLKQLVAYAGRDAFLEGARRYFKRHAYGNTRLGDLLSVLEETSGRDLAAWSRAWLETAGVNSLTPQVTLSAEGRITELAVVQEAAESHPTLRPHRVAVGLYRRSDAGDLVRYARAEVDVEGPRTAVAELVGAEAPELVLVNDDDLTYCKIRFDETSLATLREHLGGLTDPLARALCWSALWNLTRDALMPARDFIGLVLRFAGRETDIGVLQMLHAWAGTAHTHYAAPGWREEGGRLLAEGALRELRIAEPGSQHQLTWARFFASVASSEADLQLLQGLLDGTAKIDGLEVDQELRWAFQLPLAVHGVADERALAAELSRDDTASGKRHQIRCLAARPSAAVKAQAWASVVESDALSNALVEATIAGFAQPSQRGLVAEYAPKYFAAIERVWAERSIQIGMDVVRGLFPHLQDSAGTVAAADAWLSAHESAPPALRRLVLESRDDLSRALRAQECDAA
>NZ_CP023690.1|WP_150511147.1|3678241_3678883_-|DsbA-family-protein
MSETAVKTPVDFWFDPLCPWAWMTSRWVLEVEKVRDIEVSWHVMSLAVLNEDKLDELPEEYREMLATKAWGPVRVVIAAQQEHGAQVLGDLYTALGTRIHNRGEGPTKEAVAGALKEVGLPESLLDHWDETPYEAELRASHNEGIEKVGQEVGTPVIAVPGADGEQIAFFGPVVTPAPKGEAAARLWDGTLLVASTPGFYEIKRTRTQGPIFD
>NZ_CP023690.1|WP_150511157.1|3690628_3693922_+|S8-family-serine-peptidase
MTREAQKSTEDRPGARRTARLATAIAVAAALTAAAPLPLAFADETPAPAPKSAAAKLGAADAELLADAKADGDKTVTMMVATEPGSTEQVAKQLDAVEGGSVGRTYDKLGYVRAAVPTAKADAAIKAASKLSTVHGIDLRHEIELDDPKPQSAKGAGPAPGAAAAPGKDTPAKNPYNPSFETGAVDFVKKHPKADGRGITIGVIDSGVDLGHPALQKTTTGERKITDWVTATDPIVDGDGTWRRMTNPVSGPAFTWDGDTWKAPSGSFQISRFREAATTGGDAKGDLNRDGDTTDTWGVLYDPAAGTVRVDLNDNKDFTDDKAMKPYGDKHQVAYFGKDDPATDVAERVPFVVEIRKDVPTDPYGGDWVGKKADFVNIGLIESEHGTHVAGITAANKLFGGKMNGAAPGAKIVSSRACTWSGGCTNVALTEGMIDLVTKRGVDIVNMSIGGLPALNDGNNARAELYKRLIDTYGVQLVISAGNEGPGANTIGDPGLADHVISVGAAISKETWAANYGSEVAKKYAMFNFSSRGPREDGGFQPLITAPGSAINTTQTWLPGGPVAEAGYKLPAGYSMLNGTSMSSPQAAGSAALLLSAAKQQRIDLTPAKLRTALTSTADRIPGVQAYAQGTGRMDVMGAWDAIKGGAKAHEYTVKAPVDTALEQELKKPGTGLYDREGGLKAGEKKTYKVTVTRTTGPRGPVRHELKFANNHEGTFRLVGPSEVLLTRDKPVTVKVEAKPKTAGVSSARLTVNDKRTRGIDHQIMTTVVVSKELAKPKFTYTAKGSVQRNGTKSYFVTVPKGAKTLEVALGGLADKSQTRFISVHPYGLPAEETSSLVCYPNFPNPDNTCRPDLRSYKDPTPGVWEIEVESRRTSPVLDNPYTLNVSALGVSFAPAPQQVDEAKVGAATPVTWKATNDYAAVDGKLKGGSLGSAVTARPTVKQGQKQTTTVVVPEGAERLDAAIGGTSDARADLDLAVLKDGRVVGQSADGDSDESVSIAKPAAGTYTIEVAGYSIPSGQTAYDYRDVFFSASLGQVKVDEAKPVKLANGETATVAAELVAGAPAASGRVLFGEVNLLNARGTVAGTGTVTVAKVTG
>NZ_CP023690.1|WP_150511158.1|3694009_3695506_-|M28-family-peptidase
MRAPRSRATAALVSAAVAVPVLFAAAPQAGAQGDHKPHPTTQERQAKKLAKKLVEKSSGKSAYRHLEKFQEIADKNGGNRAAGTKGHKASTTYVHDRLKKAGYKVSYQDFTFYESKTLREGAAVLSPEARKLNAVAFDFSKATPEGGIQAPLAAARVDDTPGCEADDYTSNTFTGKIALVKRGACTFAEKEAAAAKAGAIGLILYNHSGDKPVHGNLETPDNAHIPAAGITLAEGEALAKQIAQGEVKVSLDVATKAVPHKTRNVIAETRGGRADRVVGLGAHLDSVAEGPGINDNGSGSAGLIEVAEKLAKATNGGKKLNNKVRFSWWSAEELGLLGSDHYVKTLTAKQKKNIKLYLNFDMIGSPNAAELVYDGDNSDNVGSGPGPKGSAQIEKLINGFLDKKKVPHWGTDFDGRSDYGPFIAEGIPAGGTFTGAEGLKTAEQAAKAGGKAGQPYDPNYHGKGDNLKNIDRKIFDVNVDVIANAVGVYAQDLGSLKR
>NZ_CP023690.1|WP_150515506.1|3695665_3696391_-|hypothetical-protein
MLAVTDGPVPDAARADEEFMAEHAAAVADVAALRKQLRAMGDTLARGPEAEPPTARPVRAPGPAGPGWRRALLALAATAAAGLLGGVVWLGARADLGSGGDGDAKSADAGSRPGELESGGDTAQRDEGGKQSGVGYVACARLIVEGTVRSVETLPGGIEDRITLDVARAYKPVKAPDEVTFVMDVNVDPPLRAGDRALIGIPEGEASPDIWSTGKGVAEERGWIVAALPKARALESRGLEC
>NZ_CP023690.1|WP_150515507.1|3696489_3697035_-|sigma-70-family-RNA-polymerase-sigma-factor
MRGKPRRQARDAADRPAQGADPLDPAQEDRVRAVLSLGGVPYGELQDGVQQVRLRLLERAAKGDGAPRDVSAWAAVVASNWAMDWHRARRRQERLGERLAALRPERPEEDGAESRVLSLAVAQGLDELPDGQRQVVVLRFYADLPVRDIAAELGIPEGTVKSRLHTAVRMLRTRLHEEEVV
>NZ_CP023690.1|WP_150511159.1|3699450_3700461_+|aspartate-semialdehyde-dehydrogenase
MKVGIVGATGQVGTVMRKILIERKFPVDELRLFASARSAGTVVDGVTVEDASTADYTGLDIVLFSAGGTTSKALAEKVASQGAVVIDNSSAWRRHPEVPLVVSEVNPHAIADRPKGIIANPNCTTMAAMPVLKPLHLEAGLTSLVVATYQAVSGSGVAGVEELYGQIEKVGADAPKLAHDGSAVDFPAPDKYVAPIAYNVLPMAGSIVDDGLNETDEEQKLRHESRKILEIPGLKVSGTCVRVPVFTGHSLQVNARFERPISPERAIEILSGAEGVVVTDVPTPLGAAGRDESFVGRVRRDETVENGLAFFISDDNLRKGAALNAVQIAELVAQES
>NZ_CP023690.1|WP_150511160.1|3700577_3701087_+|DUF1203-domain-containing-protein
MSTQYTPRPIEPKALAQLRERDDAGRPCVPYVDEEGGSPLRCCLRPIPAGDRVALVAYAPLRRWAARTGAQPGAYDEQGPVFIHADPCAGPVEADLYPFARAGALRTLRRYDARGRIVGGRLLEIPEDTTAGFDAAFEEAFADPEVTQVHVRAVEHGCLQFVVHRPEGA
>NZ_CP023690.1|WP_150511161.1|3701100_3701985_-|LysR-family-transcriptional-regulator
MGGVEIRELECFLVLADELHFGRAGARLYVSQGRVSQLLAALEQRIGARLVERTSRRVRLTPLGERFRAELSPAYAELAAVVDRAKEAARGVEGRLRIGFQGTADARLMEAITTFRKRHPACVTEIAEVPFADPFGAVRQGEVDAAIVLLPVAEPDLVLGPLFSRQQQTVAVSVRHPFAGRERLAAAELGGMPLIAAGPPAPAYWREAHAPSALPAPAVRTLQEGLTLVAADQGAMLLCRPTAAYHGREDVVFVPVDGVPDSVLGMVWHRDGETERVRAFARAVAAATVPAAAA
>NZ_CP023690.1|WP_150511162.1|3702098_3703307_+|MFS-transporter
METPVETPTETPAQTPHVDARQRALPLSVVAVAAATFSVVTTEMLPVGLLTSLASGLGVSDGTAGLTVTLPGVVAALAALLLPVAVRGADRRAVLCGLMLLLGAANLLSALAPSFAVLLAARIVVGLCIGGVWAVAASLAVRLVRAESVGRATAVIFSGIAVASVLGVPAGTFLGELASWRWAFGAVAALGLGVAALLAVVLPALPPSEPVRLGAFPALLRLPRLRVGLIAVALLVVGHFAAYTYVRPVLERVPDVGAGLVSGLLLSYGVAGIAGNFLGGTFAARDPRRALLLISAALAAVVLLLVPAGSSLPVTVALLVAWGLAYGGVSVSSQNWVMAAAPQAREAASALFAGIFNVAIALGALLGGRVADGLGATDVLWLGGGLAALALGVVATAGRGAR
>NZ_CP023690.1|WP_150511163.1|3703303_3703741_-|ATP-binding-protein
MSEDGSKPEPFPGVEPWEYTLQIPRELCAVTVCRHTLRAILSVHGLGGVVDVAELLATELVSNAVRHTKGPVSFRLLWADGVLRIGAWDADPTPPAPTSRPAPLDQEDGRGLDLIRCCSDTWGWHPLPKEGDSGKYVWCELGAAA
>NZ_CP023690.1|WP_150511164.1|3703975_3704827_+|helix-turn-helix-domain-containing-protein
MATRRNPSARQVRLGVELRRMRDAAGLKATEAAALLGASSVQMSQIEAGVAGVSEERVRRLAANYGCADSGLVEALVAMATDRTQGWWEEYQSVLPRAFGDLAELEHHATFLREVVITHVPGLFQTPDYARAVFAYMNPELPVSALEPRVEHRMRRRAAIEGAAPTPYGAVVHEFALRVRVADRRVARAQLLQLLDLSELPGVSVRVIPVDQDGFAGAGASMMYCGGPVPRLDTGIRDAPVNKRQIDADVQLRRLRTLLRMVETASLAPVPSREFIHRVAKEL

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Crispr_ID: NZ_CP023690_5

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_5

4213302-4213408

Orphan

Consensus_repeat	Method
GCCCCGACCTAGCGGCTTGCACGCCGTCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_5

>merge|NZ_CP023690|5|4213302-4213408|CRISPRCasFinder
GCCCCGACCTAGCGGCTTGCACGCCGTCGCCTGCCTTCCCCCACCCGCCCACCCGTGACACCCCAGCCATCCGGCCCGGCCCCGACCTAGCGGCTTGCACGCCGTCG

>NZ_CP023690|5|5|4213302-4213408|CRISPRCasFinder
GCCCCGACCTAGCGGCTTGCACGCCGTCG	CCTGCCTTCCCCCACCCGCCCACCCGTGACACCCCAGCCATCCGGCCCG
GCCCCGACCTAGCGGCTTGCACGCCGTCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150511500.1\|4211367_4212768_+\|cytosine-permease	unknown	unknown	gnl\|CDD\|271377
NZ_CP023690.1\|WP_150511494.1\|4203224_4204613_-\|diaminopimelate-decarboxylase	unknown	unknown	gnl\|CDD\|143505
NZ_CP023690.1\|WP_150511507.1\|4220873_4222058_-\|4-hydroxybenzoate-3-monooxygenase	unknown	unknown	gnl\|CDD\|236198
NZ_CP023690.1\|WP_150511508.1\|4222718_4223540_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224059
NZ_CP023690.1\|WP_150511506.1\|4219754_4220669_-\|Bax-inhibitor-1/YccA-family-protein	unknown	unknown	gnl\|CDD\|378959
NZ_CP023690.1\|WP_150511504.1\|4218116_4218920_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150511502.1\|4213730_4215122_-\|cystathionine-beta-synthase	unknown	unknown	gnl\|CDD\|273464
NZ_CP023690.1\|WP_150515557.1\|4215356_4216355_+\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|238874
NZ_CP023690.1\|WP_150515556.1\|4207650_4209000_+\|formimidoylglutamate-deiminase	unknown	unknown	gnl\|CDD\|236420
NZ_CP023690.1\|WP_150511505.1\|4218957_4219269_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150511503.1\|4216617_4217838_+\|acetyl-CoA-C-acetyltransferase	unknown	unknown	gnl\|CDD\|181146
NZ_CP023690.1\|WP_150511501.1\|4212809_4213238_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150511495.1\|4204730_4206389_+\|urocanate-hydratase	unknown	unknown	gnl\|CDD\|235448
NZ_CP023690.1\|WP_150511493.1\|4201757_4203119_-\|amino-acid-permease	unknown	unknown	gnl\|CDD\|129987
NZ_CP023690.1\|WP_150511496.1\|4206451_4207654_+\|allantoate-amidohydrolase	unknown	unknown	gnl\|CDD\|236456
NZ_CP023690.1\|WP_150511492.1\|4200710_4201664_+\|SigB/SigF/SigG-family-RNA-polymerase-sigma-factor	unknown	unknown	gnl\|CDD\|274373
NZ_CP023690.1\|WP_030672559.1\|4219370_4219601_+\|DUF4287-domain-containing-protein	unknown	unknown	gnl\|CDD\|379478
NZ_CP023690.1\|WP_150511509.1\|4223698_4226218_+\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226957
NZ_CP023690.1\|WP_150511498.1\|4209236_4210406_+\|imidazolonepropionase	unknown	unknown	gnl\|CDD\|237604
NZ_CP023690.1\|WP_150511499.1\|4210417_4211251_-\|MurR/RpiR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224651

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150511500.1\|4211367_4212768_+\|cytosine-permease	gnl\|CDD\|271377	cd11484, SLC-NCS1sbd_CobB-like, nucleobase-cation-symport-1 (NCS1) transporter CobB-like; solute-binding domain. This NCS1 subfamily includes Escherichia coli CodB (cytosine permease), and the Saccharomyces cerevisiae transporters: Fcy21p (Purine-cytosine permease), and vitamin B6 transporter Tpn1. NCS1s are essential components of salvage pathways for nucleobases and related metabolites; their known substrates include allantoin, uracil, thiamine, and nicotinamide riboside. NCS1s belong to a superfamily which also contains the solute carrier 5 family sodium/glucose transporters (SLC5s), and solute carrier 6 family neurotransmitter transporters (SLC6s).	6.49083e-96
NZ_CP023690.1\|WP_150511494.1\|4203224_4204613_-\|diaminopimelate-decarboxylase	gnl\|CDD\|143505	cd06836, PLPDE_III_ODC_DapDC_like_1, Type III Pyridoxal 5-phosphate (PLP)-Dependent Enzymes, Uncharacterized Proteins with similarity to Ornithine and Diaminopimelate Decarboxylases. This subfamily contains uncharacterized proteins with similarity to ornithine decarboxylase (ODC) and diaminopimelate decarboxylase (DapDC). ODC and DapDC are fold type III PLP-dependent enzymes that contain an N-terminal PLP-binding TIM-barrel domain and a C-terminal beta-sandwich domain, similar to bacterial alanine racemases. They exist as homodimers with active sites that lie at the interface between the TIM barrel domain of one subunit and the beta-sandwich domain of the other subunit. ODC participates in the formation of putrescine by catalyzing the decarboxylation of ornithine, the first step in polyamine biosynthesis. DapDC participates in the last step of lysine biosynthesis, the conversion of meso-2,6-diaminoheptanedioate to L-lysine. Proteins in this subfamily may function as PLP-dependent decarboxylases. Homodimer formation and the presence of the PLP cofactor may be required for catalytic activity.	0
NZ_CP023690.1\|WP_150511507.1\|4220873_4222058_-\|4-hydroxybenzoate-3-monooxygenase	gnl\|CDD\|236198	PRK08243, PRK08243, 4-hydroxybenzoate 3-monooxygenase; Validated.	0
NZ_CP023690.1\|WP_150511508.1\|4222718_4223540_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224059	COG1136, SalX, ABC-type antimicrobial peptide transport system, ATPase component [Defense mechanisms].	2.0237e-111
NZ_CP023690.1\|WP_150511502.1\|4213730_4215122_-\|cystathionine-beta-synthase	gnl\|CDD\|273464	TIGR01137, Cystathionine_beta-synthase, cystathionine beta-synthase. Members of this family closely resemble cysteine synthase but contain an additional C-terminal CBS domain. The function of any bacterial member included in this family is proposed but not proven. [Amino acid biosynthesis, Serine family].	0
NZ_CP023690.1\|WP_150515557.1\|4215356_4216355_+\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|238874	cd01836, FeeA_FeeB_like, SGNH_hydrolase subfamily, FeeA, FeeB and similar esterases/lipases. FeeA and FeeB are part of a biosynthetic gene cluster and may participate in the biosynthesis of long-chain N-acyltyrosines by providing saturated and unsaturated fatty acids, which it turn are loaded onto the acyl carrier protein FeeL. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	2.61932e-49
NZ_CP023690.1\|WP_150515556.1\|4207650_4209000_+\|formimidoylglutamate-deiminase	gnl\|CDD\|236420	PRK09229, PRK09229, N-formimino-L-glutamate deiminase; Validated.	0
NZ_CP023690.1\|WP_150511506.1\|4219754_4220669_-\|Bax-inhibitor-1/YccA-family-protein	gnl\|CDD\|378959	pfam12811, BaxI_1, Bax inhibitor 1 like. The Bax-inhibitor-1 region of the receptor molecules is conserved from bacteria to humans.	7.47402e-84
NZ_CP023690.1\|WP_150511503.1\|4216617_4217838_+\|acetyl-CoA-C-acetyltransferase	gnl\|CDD\|181146	PRK07851, PRK07851, acetyl-CoA C-acetyltransferase.	0
NZ_CP023690.1\|WP_150511495.1\|4204730_4206389_+\|urocanate-hydratase	gnl\|CDD\|235448	PRK05414, PRK05414, urocanate hydratase; Provisional.	0
NZ_CP023690.1\|WP_150511493.1\|4201757_4203119_-\|amino-acid-permease	gnl\|CDD\|129987	TIGR00909, putative_amino_acid_transporter, amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	1.62647e-47
NZ_CP023690.1\|WP_150511496.1\|4206451_4207654_+\|allantoate-amidohydrolase	gnl\|CDD\|236456	PRK09290, PRK09290, allantoate amidohydrolase; Reviewed.	9.46333e-175
NZ_CP023690.1\|WP_150511492.1\|4200710_4201664_+\|SigB/SigF/SigG-family-RNA-polymerase-sigma-factor	gnl\|CDD\|274373	TIGR02980, SigBFG, RNA polymerase sigma-70 factor, sigma-B/F/G subfamily. This group of similar sigma-70 factors includes clades found in Bacilli (including the sporulation factors SigF:TIGR02885 and SigG:TIGR02850 as well as SigB:TIGR02941), and the high GC gram positive bacteria (Actinobacteria) where a variable number of them are found depending on the lineage.	4.1222e-122
NZ_CP023690.1\|WP_030672559.1\|4219370_4219601_+\|DUF4287-domain-containing-protein	gnl\|CDD\|379478	pfam14117, DUF4287, Domain of unknown function (DUF4287). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 70 and 180 amino acids in length.	7.16996e-24
NZ_CP023690.1\|WP_150511509.1\|4223698_4226218_+\|ABC-transporter-permease	gnl\|CDD\|226957	COG4591, LolE, ABC-type transport system, involved in lipoprotein release, permease component [Cell envelope biogenesis, outer membrane].	8.72423e-28
NZ_CP023690.1\|WP_150511498.1\|4209236_4210406_+\|imidazolonepropionase	gnl\|CDD\|237604	PRK14085, PRK14085, imidazolonepropionase; Provisional.	0
NZ_CP023690.1\|WP_150511499.1\|4210417_4211251_-\|MurR/RpiR-family-transcriptional-regulator	gnl\|CDD\|224651	COG1737, RpiR, Transcriptional regulators [Transcription].	2.31518e-31

>NZ_CP023690.1|WP_150511501.1|4212809_4213238_+|hypothetical-protein
MEATRDAELKKELDAALHARKDLGEEYESALVDSFLEKVEKRLDGTIDRQMRRHLAEQQMIMARSARNPSSGVDSWGERFGFGIVSLILAIPLSAIGVVNAGLSGLFVTWFGIVGVNAVHAVRGTGLLPLLRRSPRKPDWED
>NZ_CP023690.1|WP_150511500.1|4211367_4212768_+|cytosine-permease
MTESPKSLVERRSIDVVPDAERHGRAFSQFTLWLGANLQITAVVTGALAVVFGGDVVWSVVGLALGNVVGGAVMALHSAQGPKLGLPQMIQSRAQFGVRGAVVPLLLVILMYVGFFASGSVLAGQATAELTHTGDTTGIVLFAAVTAVTAAVGYRVIHVLGRIASVVCALAFVYLGIRLLDRVDLSALLADARFDLPVFLLAVSLSASWQLAFGPYVADYSRYLPRTTSARATFWWTLSGSALGSQWSMTFGVLVAASAGGVFLDDQVAYVVELGGTGLVASLLYFVIALGKLTINVLNTYGGFMSMVTSIGGFRTQKEISPRGRAAYIGLIMVVGTTVALLGKDSFLTSFKDFLLFLLTFFTPWSAINLVDYYLISKERYDIPALFDPHGRYGAWRWDALTVYGVGLLAQLPFLVTHFYTGPLVDPLGGADVSWIVGLVVPALLYWLLARRAPATGGLAQDGMGG
>NZ_CP023690.1|WP_150511499.1|4210417_4211251_-|MurR/RpiR-family-transcriptional-regulator
MSDSPAARLQVLFEGHRLTPTQRRIAHCMVRRAADAPFLSSVELAELAGVSQPSVTRFAVALGFDGYPALRRHLRDVAPAEAPEDAEANEYQQAVEAEIENLRHLAAVLADPAPVERAGRLLAASRPLPVLGLRAAASQAYGFSYFAAKVHPDVRLLDEGGSMLTDRLDAAVRAGATVLLCFALPRHPREAVDALAHAQGAGLTVVTVADSAFAPVAAHSDLLLPAAVGTGLAFDTACAPMLLGRALLEAMCDALPDAQARLEEFDAGAAERGLFVE
>NZ_CP023690.1|WP_150511498.1|4209236_4210406_+|imidazolonepropionase
MTTTVIRNIGSLVTNDPALGQGPLGLVEDAAVVLDGEEVAWVGPGAQAPAADEAYDAEGRAALPGFVDSHSHLLFAGDRTQEFNARMEGRPYEAGGIRTTVAATRAAPDEALEANLARYLAEALRQGTTTFETKSGYGLTTEDEARALRIARRHTDEVTFLGAHIVSPDFAADPAAYVALVTGEMLDACAPHARWIDVFCEKGAFDGDQARAILTAGKARGLHPRVHANQLSYGPGVQLAVELDAASADHCTHLTDADVDALAHSGTVATLLPGAEFSTRAEWPDARRLLDAGATVALSTDCNPGSSFTSSVPFCVALAVRDMGMTPDEAVWAATAGGAAALRRTDVGRLSPGARADLALLDAPSHVHLAYRPGVPLVSAVWRRGARVA
>NZ_CP023690.1|WP_150515556.1|4207650_4209000_+|formimidoylglutamate-deiminase
MTHTYWAEQAWLDPVVEPGVALDVGADGRIAAVRTGVEAPPPGATVLRGLTIPGLANAHSHAFHRALRSTVQVGSGTFWTWREVMYSVADRLTPETYHELARAVYAEMALAGVTAVGEFHYLHHAPGGKRYADPNAMGEALIAAAADAGIRITLLDTAYVAAGLRDATEGEPPNHHQLRFSDGTAEAWAERAALLKDREHARVGAAVHSVRAVPARQLGTVVEWAASRGVPLHVHLSEQTAENEACLAVHGCTPTRLLADHGALGARTTGVHNTHLTDADIALIGGSGTGTCMCPTTERDLADGIGPAPALQRAGSPLSLGSDSHAVIDLFEEARAMELNERLRSHTRGHWTAAALLRAASADGHAALGWADAGALAPGALADFATVALDSVRTAGAAARLGAEVAVFAASAADVRHTVVGGRHVVRDGAHTLLPDVPSSLARAVAALH
>NZ_CP023690.1|WP_150511496.1|4206451_4207654_+|allantoate-amidohydrolase
MWADLSPIGRDAETGGYRRYAWTGADADCRTWFQEQAESRGLAYETDRNGNQWAWLGDPAAGDAVVTGSHLDSVPDGGAFDGPLGVVSSFAALDELRARGVEFTRPLALTNFGDEEGARFGLACVGSRLTAGQLTKEQAYELRDGDGVRLPEAMEAAGYDPSAIGPDPERLAGIGAFVELHVEQGRALDLSGDEVGIASAIWPHGRWRFDFRGEANHAGTTRLVDRRDPMLSYAETVLAARREAELAGAVATFGKISVEPNGVNAIPSLVRGWLDSRAADQDTLDTVVTAVEKAAREYADRHGVDLAVVRESFTPVIEFEHALRDELGAILRGRTGREVPVLGTGAGHDAGILSASVPTAMLFVRNPTGVSHSPAEHAAEDDCLAGVRALADVLEGLACR
>NZ_CP023690.1|WP_150511495.1|4204730_4206389_+|urocanate-hydratase
MSGPRPVRAPRGTELSALGWQQEAALRMLQNNLDPEVAEHPDKLVVYGGTGKAARDWRSFDAMVRTLKTLKQDETMLVQSGRPVGVMQTHEWAPRVLIANSNLVGDWANWEEFRRLEALGLTMYGQMTAGSWIYIGTQGILQGTYETFAAVAAKKFGGTLAGTITLTAGLGGMGGAQPLAVTMNDGVAICIDCDPRAIERRIEHRYLDVKADSLEHALQLATEARDARRPLSIGLLGNAAELLPRMLAEGAPVDIVTDQTSAHDPLAYLPVGVDFDDMATAAEKDPAGFTQRARESMAQHVEAMVGFMDAGAEVFDYGNSIRGEAQLAGYERAFAFPGFVPAYIRPLFCEGKGPFRWAALSGEASDIHKTDKAILDLFPENESLHRWIKMAGERVHFQGLPARICWLGYGERDKAGERFNDMVASGELQAPLAIGRDHLDCGSVASPYRETEGMRDGSDAIADWPLLNAMVNVASGASWVSLHHGGGVGMGRSIHAGQVSVADGTKLAGEKVRRVLTNDPGMGVIRHVDAGYESADAVADDRGVRIPMREGE
>NZ_CP023690.1|WP_150511494.1|4203224_4204613_-|diaminopimelate-decarboxylase
MSLDDATVPGPTVDPTSPPGAEAAARRDQAVRAAIEQGLVSPENPLAGLIDVTGVRAAATALRAAFAGVTPPGTPVLHAFAVKATPLVPVLRLLREEGIGAEVASPGELALARAAGVPPAHTVLDSPAKTPAELREALALGIAVNADNSQELARIDALVRSAPTGAPLGVRVNPQVGAGSIGALSTATATSKFGVPLRDEGAREWLVRAYLDRPWLTRVHAHTGSQGIPLDLLVRGVAAVYELAEEINARAGRRQVDTLDIGGGLPVNFASDEADPTHGAYARLLKERVPGLLDGRYGLVTEFGRSLLAKQGVLLARVEYVKEAGGRPIALTHAGVQVATRTVYAPESWPLRLAAYDAKGRPKQGPAVGQDVAGPACFAGDLLAADHPLPRLEAGDHVAALDTGAYYFAQHYSYNSLPRPGIHGFAARADGTVRFATVRAPQPVAELVAEAGGGVPDALDGL
>NZ_CP023690.1|WP_150511493.1|4201757_4203119_-|amino-acid-permease
MTTSGTSGSTTHPAEEEPGLRRVLGPKLLILFVIGDILGTGIYATTGKVAGKVGGALWLPFLIGFVVAILTAASYVELVGKYPKAAGAALYTQKAFKVPFLTFIIAFMVMCSGLSSASAAARAFSGDYLSELTDDALPPTLVAIAFILALAALNLRGVSESVKTNVVLTVVELTGLLIILAIGAWAVLTGDGEPSRLTEFEASGTGYALLTGVLGATALGFFAFVGFEDSVNMAEETKDPTRTFPRAIFIGVAVTGTIYVLVALVSSLLVDYETLEGSSGPLLEVVKAGGVDFPHKLFALIALFAVTNSALINIMMASRLCYGMANERILPRAMGRVLAGRRTPVVGIAFVSLLAIGLVSTGEIEGLGDTTAFLLLCVFAVVNVAVLVLRRDPVAHDHFRAPTVLPVLGAITALVLASPLADRPAEVYIRAGVLLVIGIALWAVNKLAMTVRA
>NZ_CP023690.1|WP_150511492.1|4200710_4201664_+|SigB/SigF/SigG-family-RNA-polymerase-sigma-factor
MSPRLDESRTDQATSTPPPNRTRTTIPGPAEEALPPAATDPSHTGERPETLSGLPEIPPFDEVGPLDARALSKTLFERLDSLEEGTHAYAYVRNTLVELNLALVKFAASRFRSRSEPMEDIIQVGTIGLIKAIDRFELSRGVEFPTFAMPTIVGEIKRFFRDTSWSVRVPRRLQELRLDLAKAGDELAQQLDRSPTVAELAERLGISHDEVVEGMAASNAYTASSLDAQPEEDDSEGALADRIGYEDHGLEGIEYVESLKPLIADLPPRDRKILSLRFVANMTQSEIGEELGISQMHVSRLLSRTLVRLRRGLTVEE
>NZ_CP023690.1|WP_150511502.1|4213730_4215122_-|cystathionine-beta-synthase
MQFHDSMTSLVGNTPLVRLNNVTQGLKATVLAKVEYFNPGGSVKDRIALRMIEAAEASGELRPGGTIVEPTSGNTGVGLAIVAQQKGYKCVFVCPDKVSTDKINVLRAYGAEVVVCPTAVDPEHPDSYYNVSDRLVREIPDAWKPDQYSNPNNPLSHYHSTGPELWEQTDGKITHFVAGIGTGGTISGTGGYLKEVSGGKVRIVGADPEGSVYSGGSGRPYLVEGVGEDFWPTAYDRNVTDEIVAVSDKDSFQMTRRLAKEEGLLVGGSCGMAVVAALRVAEGLGPDDVVVVLLPDSGRGYMSKIFSDEWMNDYGFLEEAGDQPRVGDVLSRKEGGELPSLVHMHPEETVGEAIEVLREYGVSQMPIVKPGAGHPDVMAAEVIGSVVERELLDALFAQRASLHDPLEKHMSDPLPQVGSGEPVGDLMSVLGGADAAIVLVEGKPTGVVSRQDLLAFLAEQQGS
>NZ_CP023690.1|WP_150515557.1|4215356_4216355_+|SGNH/GDSL-hydrolase-family-protein
MARRIAAGAAYGGGGIGLLGAATVGLVLAEVQLAKRSVGNGGHGAPPRADGRYGAAFAARAACGEPLRFAMLGDSTAAGLGVHRARQTPAALLASGLAAVAERPVDLRVVAKAGAQSDDLDRQVTLVLSDETGPVPDVCVVMIGANDVTHRMPPTRSVRLLASAVRRLRTAGAEVVVGTCPDLGTIEPVYQPLRWLARRVSRQLAAAQTIGVVEQGGRTVSLGDLLGPEFAANPRELFGPDNYHPSAEGYATAAMAVLPTLCAALGLWPEEERPDVSRREGFLPVARAAARAAAEGGTEVTGAIPSGPRGPFALLKRRRRRRIQTPDPSPIG
>NZ_CP023690.1|WP_150511503.1|4216617_4217838_+|acetyl-CoA-C-acetyltransferase
MPEAVIVSAARSPIGRAFKGSLKELRPDDLTATIVQAALAKIPALDPRDIDDLMLGCGLPGGEQGHNLGRIVAVQMGMDHLPGCTITRYCSSSLQTSRMALHAIKAGEGDVFVSAGVEMVSRSVKGSSDGLPDTHNPLFADAEARTAARAEQTGTNWHDPREDDLVPDAYIAMGQTAENLARLKGVTRQDMDEFGVRSQNLAEEALKNGFWEREITPVTLPDGTVVAKDDGPRAGVTMEGVAGLKPVFRPDGLVTAGNCCPLNDGAAALVIMSDTKARELDLTPLARIVSTGVSALSPEIMGLGPVEASKQALKRAGLGIGDIDLVEINEAFAAQVIPSYRDLGIPLDKLNVNGGAIAVGHPFGMTGARITGTLINSLQFHDKQFGLETMCVGGGQGMAMVIERLS
>NZ_CP023690.1|WP_150511504.1|4218116_4218920_+|hypothetical-protein
MSLALLLSAAAATAVGAASLHTVRGLRQQITDLRTELAESHATTGGRATVPAARTTVDTDEIRAAVADALAEERERELAEARAFWAAQEARDIADAPSLLGGLPESIADELFLPRQADLAGLESDSLEPVVEPFADPDEFAGDSAELAAARRRHPSHPDFVPVQSPAYTDHERTVACLEELADARTALADVRPGPLGTLDVYVFADGTTLCMTPGHRETAELLAAALRDGKAPVLLGGSGVSGAYALTFACGTENVYILADRVIASV
>NZ_CP023690.1|WP_150511505.1|4218957_4219269_-|hypothetical-protein
MLDTTPLIAAVDRFADRLRAAPQSRLQRGAAAEALALARELAVRSQLSEEPGAEPRVMPDAGMFAAADQITVAGRDLAVVLRDEEELTEAVRLVEEALARAGV
>NZ_CP023690.1|WP_030672559.1|4219370_4219601_+|DUF4287-domain-containing-protein
MSQVFSEETHRNLLARIPHCTGREVSDWLRTVDEGPSLFRFEEKVSWLRGEHNLAYGHAKAIIHEYDLRRAARKLG
>NZ_CP023690.1|WP_150511506.1|4219754_4220669_-|Bax-inhibitor-1/YccA-family-protein
MRSSNPVFSRRGFSRDNGYAGFNAQPQAGGPAVATQGNAYAPGNPYAGQQAPTNPYAANPYGQQDLQGAPPQAPVTTGRMTMDDVVMRTATTLGVLVVTAALAWALLPVDDANISKSYGIAIGAGLVAMVLGFVQAFKRKASPPLILAYAALEGVFLGVVSSVVDNRIASGAAMQAVLGTMAVFLAVLVAYKAGWIRVNRRFYGFVMAAALGFVLLMAVNLLFSVFGGGDGLGFRSGGLGIMFGIIGVLLGACFLALDFKQVEDGIAYGAPREEAWLAAFGLTMTLVWIYLEFLRLIAILQGND
>NZ_CP023690.1|WP_150511507.1|4220873_4222058_-|4-hydroxybenzoate-3-monooxygenase
MRTQVGIIGAGPAGLVLARLLHAAGIETVVIEARDRSYVEGRQRAGILEHGTADILRAAGAGERMDREGHRHDGIELRFDRRRHRVDFPSLTGGRSVMVYAQTEVCKDLIALRLRDGGPLLFGAEALAVEGADTGRPRVRYRHEGRERTLECAYVAGCDGFWGVARAAVPAALSRTYERAYPYGWLGVLADAPPSHDELVYARHDRGFALLSHRSPTVSRLYLQVPADTDPAAWGDTQIWDELERRCATEGGGRLTRGPLTAKSVTPLRSYVHEPMRYGRLFLAGDAAHIVPPTGAKGLNLAVGDVATLARALVAHARTGDTALLDAYSATCLRRVWQAERFSNALTALLHRHPDATPFDDRLQLAQLDRVATSRPARADLAEAYTGRPLDGVL
>NZ_CP023690.1|WP_150511508.1|4222718_4223540_+|ATP-binding-cassette-domain-containing-protein
MDEVPPTPSYRQEHPPVTTTTAFAAHATAVAARATDLSKVYGQGETQVVALDRVSVDFGQGRFTAIMGPSGSGKSTLMHCVAGLDSFSSGSVRIGETELSTLKDKQLTKLRRDKIGFIFQAFNLLPTLTALENITLPMDIAGRKVDKQWLEQVISMVGLAGRLSHRPTELSGGQQQRVAVARALASKPEIIFGDEPTGNLDSRSGAEVLGFLRNSVRELGQTVVMVTHDPVAASYADRVIFLADGRVVDEMHQPSAERVLDRMKDFDAKGRTS
>NZ_CP023690.1|WP_150511509.1|4223698_4226218_+|ABC-transporter-permease
MFRTALRNVLAHKARLLMTVLAVMLGVAFVSGTLVFTDTFGSAYKNKSAKSFDHVSVAIRPDGGSSHDDGQEAKQPPRLTDALLTEAGKLPGAGSVIGTYSGFTALADKDGKLVGGEWGTTGANYYPGKDGKDPRYDFAAGKAPRSAGEIALDSRTADRTGYGVGDAVRYSTDGPVKTAKVSGVFDTDDGSVVAGGSLVLFDNDTARKVLGKTEYDEIDVKAAAGTSETALKGAVEKILPKDTEAETGVSLKDEQDRMIEQNTSSMSQVLLIFAGIALFVGIFIIANTFTMLVAQRTKELALMRAVGASRRQVTRSVLIEAFIVGLVAAVAGFALGIGVAVGLEALMNAGGASLPDGPLVIGPTTIITALLIGVVVTMLAAWLPGRRAAKIPPVAAMNSVHASPTTRGLVVRNSIGSLIVALGAVMLFMDDNYVKSGGAATILVGVIVLTPLLSRPFIAAAGPLLKPFGVTGKLARLNSVRNPRRTASTASALMIGLTLITAMTVVAVSMGSAINKMATDSLKADYAVSMANFQPLTPAVHDKLAELPEVEASSALRTTWGEADGRDTRISGVDPQDFDKLVGLDFTSGSAAGLKGDAVLVDKETADAKGLKAGDTVPVKFDDDRTTRLKVAGVYKSNEMLNGLFTPTSVVTPHLSKIQDQQVLLKMKDGASDRAEDAIVKALGDNPAIKIQDKDDISNEVGGAINLLLNMLYGLLAMAILVAVLGVINTLAMSVFERKHEIGMLRAIGLDRAKIKQMVRLESVVISLFGAVLGVGLGLFLGWVAGDSISGSVKTYTMEIPAGRILVFLAIAAVVGVLAAVWPARSAARLNPLQAIKSD

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Crispr_ID: NZ_CP023690_6

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_6

5114206-5114314

Orphan

Consensus_repeat	Method
GTGCCGGTGGTGCCCTCGCAGGCTTT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_6

>merge|NZ_CP023690|6|5114206-5114314|CRISPRCasFinder
GTGCCGGTGGTGCCCTCGCAGGCTTTTCGCCGGGGTGGGGTGGGCGGTGAGTCTGCCCCTCGGTGTTGCGATGGCTGGGCCTGGTGCCGGTGGTGCCCTCGCAGGCTTT

>NZ_CP023690|6|6|5114206-5114314|CRISPRCasFinder
GTGCCGGTGGTGCCCTCGCAGGCTTT	TCGCCGGGGTGGGGTGGGCGGTGAGTCTGCCCCTCGGTGTTGCGATGGCTGGGCCTG
GTGCCGGTGGTGCCCTCGCAGGCTTT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150512149.1\|5114884_5115208_+\|TfoX/Sxy-family-protein	unknown	unknown	gnl\|CDD\|377438
NZ_CP023690.1\|WP_150512151.1\|5115803_5116214_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319924
NZ_CP023690.1\|WP_150512150.1\|5115242_5115719_+\|NUDIX-domain-containing-protein	unknown	unknown	gnl\|CDD\|240040
NZ_CP023690.1\|WP_150512148.1\|5111792_5113358_+\|DHA2-family-efflux-MFS-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|129794
NZ_CP023690.1\|WP_150512156.1\|5119498_5120092_+\|DUF4291-family-protein	unknown	unknown	gnl\|CDD\|379483
NZ_CP023690.1\|WP_150512146.1\|5108024_5109287_-\|SGNH/GDSL-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|238868
NZ_CP023690.1\|WP_170316471.1\|5109485_5110394_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|223656
NZ_CP023690.1\|WP_150512145.1\|5107637_5108015_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512144.1\|5106367_5107438_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|130256
NZ_CP023690.1\|WP_150512147.1\|5110400_5110847_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_144320016.1\|5110913_5111657_-\|TetR/AcrR-family-transcriptional-regulator-C-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|367243
NZ_CP023690.1\|WP_150515636.1\|5117770_5118166_-\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP023690.1\|WP_150512143.1\|5105525_5106371_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|366444
NZ_CP023690.1\|WP_150515637.1\|5120178_5120862_-\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|380061
NZ_CP023690.1\|WP_150515634.1\|5104574_5105405_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512152.1\|5116541_5117378_-\|glucose-1-dehydrogenase	unknown	unknown	gnl\|CDD\|235500
NZ_CP023690.1\|WP_150512154.1\|5118215_5119151_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|379262
NZ_CP023690.1\|WP_150512142.1\|5103500_5104517_-\|endonuclease/exonuclease/phosphatase-family-protein	unknown	unknown	gnl\|CDD\|377028
NZ_CP023690.1\|WP_150512155.1\|5119113_5119374_+\|DUF397-domain-containing-protein	unknown	unknown	gnl\|CDD\|377231
NZ_CP023690.1\|WP_150512153.1\|5117310_5117781_-\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380376

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150512149.1\|5114884_5115208_+\|TfoX/Sxy-family-protein	gnl\|CDD\|377438	pfam04993, TfoX_N, TfoX N-terminal domain. TfoX may play a key role in the development of genetic competence by regulating the expression of late competence-specific genes. This family corresponds to the N-terminal presumed domain of TfoX. The domain is found as an isolated domain in some proteins suggesting this is an autonomous domain.	1.53816e-10
NZ_CP023690.1\|WP_150512151.1\|5115803_5116214_+\|VOC-family-protein	gnl\|CDD\|319924	cd07263, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) family. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	6.2896e-48
NZ_CP023690.1\|WP_150512150.1\|5115242_5115719_+\|NUDIX-domain-containing-protein	gnl\|CDD\|240040	cd04684, Nudix_Hydrolase_25, Contains a crystal structure of the Nudix hydrolase from Enterococcus faecalis, which has an unknown function. In general, members of the Nudix hydrolase superfamily catalyze the hydrolysis of NUcleoside DIphosphates linked to other moieties, X. Enzymes belonging to this superfamily require a divalent cation, such as Mg2+ or Mn2+, for their activity. They also contain a highly conserved 23-residue nudix motif (GX5EX7REUXEEXGU, where U = I, L or V), which forms a structural motif that functions as a metal binding and catalytic site. Substrates of nudix hydrolases include intact and oxidatively damaged nucleoside triphosphates, dinucleoside polyphosphates, nucleotide-sugars and dinucleotide enzymes. These substrates are metabolites or cell signaling molecules that require regulation during different stages of the cell cycle or during periods of stress. In general, the role of the nudix hydrolase is to sanitize the nucleotide pools and to maintain cell viability, thereby serving as surveillance & "house-cleaning" enzymes. Substrate specificity is used to define families within the superfamily. Differences in substrate specificity are determined by the N-terminal extension or by residues in variable loop regions. Mechanistically, substrate hydrolysis occurs by a nucleophilic substitution reaction, with variation in the numbers and roles of divalent cations required.	5.16548e-30
NZ_CP023690.1\|WP_150512148.1\|5111792_5113358_+\|DHA2-family-efflux-MFS-transporter-permease-subunit	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	2.19342e-71
NZ_CP023690.1\|WP_150512156.1\|5119498_5120092_+\|DUF4291-family-protein	gnl\|CDD\|379483	pfam14124, DUF4291, Domain of unknown function (DUF4291). This family of proteins is functionally uncharacterized. This family of proteins is found in bacteria and eukaryotes. Proteins in this family are typically between 190 and 214 amino acids in length. There are two conserved sequence motifs: VYQAY and RMTW.	2.75026e-110
NZ_CP023690.1\|WP_150512146.1\|5108024_5109287_-\|SGNH/GDSL-hydrolase-family-protein	gnl\|CDD\|238868	cd01830, XynE_like, SGNH_hydrolase subfamily, similar to the putative arylesterase/acylhydrolase from the rumen anaerobe Prevotella bryantii XynE. The P. bryantii XynE gene is located in a xylanase gene cluster. SGNH hydrolases are a diverse family of lipases and esterases. The tertiary fold of the enzyme is substantially different from that of the alpha/beta hydrolase family and unique among all known hydrolases; its active site closely resembles the Ser-His-Asp(Glu) triad found in other serine hydrolases.	5.50762e-90
NZ_CP023690.1\|WP_170316471.1\|5109485_5110394_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|223656	COG0583, LysR, Transcriptional regulator [Transcription].	1.31253e-31
NZ_CP023690.1\|WP_150512142.1\|5103500_5104517_-\|endonuclease/exonuclease/phosphatase-family-protein	gnl\|CDD\|377028	pfam03372, Exo_endo_phos, Endonuclease/Exonuclease/phosphatase family. This large family of proteins includes magnesium dependent endonucleases and a large number of phosphatases involved in intracellular signalling. This family includes: AP endonuclease proteins EC:4.2.99.18, DNase I proteins EC:3.1.21.1, Synaptojanin an inositol-1,4,5-trisphosphate phosphatase EC:3.1.3.56, Sphingomyelinase EC:3.1.4.12, and Nocturnin.	1.28838e-20
NZ_CP023690.1\|WP_150512144.1\|5106367_5107438_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|130256	TIGR01188, drrA, daunorubicin resistance ABC transporter ATP-binding subunit. This model describes daunorubicin resistance ABC transporter, ATP binding subunit in bacteria and archaea. This model is restricted in its scope to preferentially recognize the ATP binding subunit associated with effux of the drug, daunorubicin. This transport system belong to the larger ATP-Binding Cassette (ABC) transporter superfamily. The characteristic feature of these transporter is the obligatory coupling of ATP hydrolysis to substrate translocation. The minimal configuration of bacterial ABC transport system: an ATPase or ATP binding subunit; An integral membrane protein; a hydrophilic polypetpide, which likely functions as substrate binding protein. In eukaryotes proteins of similar function include p-gyco proteins, multidrug resistance protein etc. [Transport and binding proteins, Other].	1.64687e-126
NZ_CP023690.1\|WP_144320016.1\|5110913_5111657_-\|TetR/AcrR-family-transcriptional-regulator-C-terminal-domain-containing-protein	gnl\|CDD\|367243	pfam02909, TetR_C, Tetracyclin repressor, C-terminal all-alpha domain.	7.09185e-10
NZ_CP023690.1\|WP_150515636.1\|5117770_5118166_-\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	2.5372e-19
NZ_CP023690.1\|WP_150512143.1\|5105525_5106371_-\|ABC-transporter-permease	gnl\|CDD\|366444	pfam01061, ABC2_membrane, ABC-2 type transporter.	1.85975e-24
NZ_CP023690.1\|WP_150515637.1\|5120178_5120862_-\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|380061	pfam17932, TetR_C_24, Tetracyclin repressor-like, C-terminal domain. TetR family regulators are involved in the transcriptional control of multidrug efflux pumps, pathways for the biosynthesis of antibiotics, response to osmotic stress and toxic chemicals, control of catabolic pathways, differentiation processes, and pathogenicity. The TetR proteins identified in overm ultiple genera of bacteria and archaea share a common helix-turn-helix (HTH) structure in their DNA-binding domain. However, TetR proteins can work in different ways: they can bind a target operator directly to exert their effect (e.g. TetR binds Tet(A) gene to repress it in the absence of tetracycline), or they can be involved in complex regulatory cascades in which the TetR protein can either be modulated by another regulator or TetR can trigger the cellular response. TetR regulates the expression of the membrane-associated tetracycline resistance protein, TetA, which exports the tetracycline antibiotic out of the cell before it can attach to the ribosomes and inhibit protein synthesis. TetR blocks transcription from the genes encoding both TetA and TetR in the absence of antibiotic. The C-terminal domain is multi-helical and is interlocked in the homodimer with the helix-turn-helix (HTH) DNA-binding domain. This entry represents the C-terminal domain present in family members such as HTH-type transcriptional repressor KstR2 as well as fatty acid metabolism regulator proteins. In Mycobacterium smegmatis, KstR2 is involved in involved in cholesterol catabolism, while YsiA in Bacillus subtilis is involved in fatty acid degradation.	4.66198e-08
NZ_CP023690.1\|WP_150512152.1\|5116541_5117378_-\|glucose-1-dehydrogenase	gnl\|CDD\|235500	PRK05557, fabG, 3-ketoacyl-(acyl-carrier-protein) reductase; Validated.	1.21376e-74
NZ_CP023690.1\|WP_150512154.1\|5118215_5119151_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|379262	pfam13560, HTH_31, Helix-turn-helix domain. This domain is a helix-turn-helix domain that probably binds to DNA.	4.41174e-07
NZ_CP023690.1\|WP_150512155.1\|5119113_5119374_+\|DUF397-domain-containing-protein	gnl\|CDD\|377231	pfam04149, DUF397, Domain of unknown function (DUF397). The function of this family is unknown.	8.46121e-20
NZ_CP023690.1\|WP_150512153.1\|5117310_5117781_-\|cupin-domain-containing-protein	gnl\|CDD\|380376	cd06121, cupin_YML079wp, Saccharomyces cerevisiae YML079wp and related proteins, cupin domain. This family includes eukaryotic, bacterial, and archaeal proteins homologous to YML079wp, a Saccharomyces cerevisiae cupin-like protein of unknown function that structurally resembles plant seed storage and ligand-binding proteins (canavalin, glycinin, auxin binding protein) as well as the bacterial RmlC epimerase. YML079wp is non-essential in yeast and localizes to the nucleus and cytoplasm. The presence of a hydrophobic ligand within a well-conserved binding pocket inside the cupin beta-barrel and sequence similarity with bacterial epimerases suggests a possible biochemical function for YML079wp and its homologs. Also included in this family are Shewanella oneidensis So0799, Agrobacterium fabrum Atu3615 and Branchiostoma belcheri Bbduf985. Proteins in this family belong to the cupin superfamily with a conserved "jelly roll-like" beta-barrel fold and forms a homodimer.	2.31005e-56

>NZ_CP023690.1|WP_150512148.1|5111792_5113358_+|DHA2-family-efflux-MFS-transporter-permease-subunit
MDGLAAQGKDDRGEETGGAAPVRDPKRWLILVVLCLSTLVLVVDNMILTVAIPPIAEDIDATASDIQWILDSYMLVFAGLLLTSGSLSDRFGRRKVMVIGLVLFGAASLIATIANSPEQLIAGRVLMGIGGALIMPSTLSILITVFDEEERPRAIAAWSAVAMVGLVGGPVFGGALLGHFWWGSVFLINLPIVGLAIIAALILMPESKGPWRKADPLGIVLSVVGMVALVWTITEWPKEGFDHPKVFVAGIVAVVALVGFAFWETRVDEPMVPIELFRNRVFTGASFSIVLLTFANGGLLLVLTQYLQFVLHYSPTKTGWAFAPLAVASLVFNTLGATLGQKLGNRVLVAVGLTITAGGFFTLTTLEPGDGFSIVAVAMVLMGMGGGLAMPAAVAALMSAVPGEHAGVGSALNDTVQQAGAALGVALLGSVLSSTYAKEMPASAGDVADNSVVEGLAEAARTGNAALGDAVRSAFTDAMSATFVTGAAAVLVAAVLSLFLMKPGPDAPAVDEDREPDLVSH
>NZ_CP023690.1|WP_144320016.1|5110913_5111657_-|TetR/AcrR-family-transcriptional-regulator-C-terminal-domain-containing-protein
MPRTGKPTAISVWTRPQRPRRDQPALSREQIVSEAIALLDAEGIEALSMRKLGTRLNAGATSLYTHVSNKDEIIELAVDQVYGEIEVPQPVSGSHEDWLAAAKQFAENVRATLLRHPWIASVLGELGMAHLGPNMMGLTEEMLGLFESGGFDLETSEIAGKTIWAYVIGVALTEAAYLTTLARSGRAEQEWHDMIQPAAAEAVQAYPRLRKMYAMGPRGADAISARQGFFEVGIACILDGLQTHAAH
>NZ_CP023690.1|WP_150512147.1|5110400_5110847_-|hypothetical-protein
MTSPERDTWRAAPSGPADDDSGWATGGTLFAGVLMFVYGILSVLEGIAGIAKDDVYARIGDYVYKFNLTTWGWIHLVLGVLVAVTGWGILKGADWARATGIALAAVAMVAQFLWLPYTPLWALISLAIGAFIIWALCTDGSRDGATAP
>NZ_CP023690.1|WP_170316471.1|5109485_5110394_+|LysR-family-transcriptional-regulator
MERQELETFLTLAEELHFGHTAERLLVSQARVSQTVKKLERSIGGTLFERTSRVVRLSPLGRQLYEDLAPLHRLMEEAVARAKDVARGVEGELGVGFLGAGAGALTQPILKLFRERCPRCEVRMRETQFRDPLGPLRSGDVDVLFTCLPVEEPDLTVGPVVIRRPRVLAMPVDHRLAGRASLSWEDLAGETCFGVVNSAPSYWWDFQVPPRTPSGREIRRGQAVATFQELMTLIATGQGVSPVIASVETYYARPDIAFVPVPDLPAAEVAAVWRTGTPSAPARAFAQAVHDTLEANGGPAAF
>NZ_CP023690.1|WP_150512146.1|5108024_5109287_-|SGNH/GDSL-hydrolase-family-protein
MSSRTRRSVVAATALALVAGLSTAGASASTDGGTQWNAAWAASPQRPSTGFTPNWSEAGFDHHTLRQVVRVTQGGDRARIRLSNAYGASPLRVEGATVARTQGTKGAAVEKGTLRRLTFGGKRSVTVPAGGQLSSDAAALGLDRFDSVTVTLRLARTTGPATFHAQSFATSYRAAGDHLTDTGGGAFGESTESWYYLSGVDVRGERPARRDGVVLFGDSITDGFGSSADGNRRWSDALAERLAAAGAPRPVVNSGIGGNLVLNDSAWFGDKSSTRFARDVTELPNARTVVVLEGVNDIGFSETDKPVYKPAPVVTAKQLINGHRKLIRAARAKGLKVVGATLVPFGGSDHYGERAAAVSDAFNTWVRTSGEYDGYVDFDKALADPKDPERIRPAYDSGDHLHPNDAGYRAMARAVDLKAL
>NZ_CP023690.1|WP_150512145.1|5107637_5108015_+|hypothetical-protein
MALTAHGSPGIRSLSHVWAGPLVLAVVYGVWAAGIHRDGGPITGGNVLYGVVTGVAFGALYAAVRRFAPGLPRELRALAWATFAGVGFGFLYSLTDASVLRSTGMAAVVAGSVFAATFYYFYTHE
>NZ_CP023690.1|WP_150512144.1|5106367_5107438_-|ATP-binding-cassette-domain-containing-protein
MTSTQPGRGPGPDGLAIETAGLVKTFGENRAVDGVDLAVPAGTVYGLLGPNGAGKTTTVKMLATLLRPDGGEAHVFGHDVVREADAVRTRVSLTGQYASVDEDLTGTENLVLLARLTGHGKKASYARAEQLLAAFGLAEAAGRQVKNYSGGMRRRIDIAASILNTPDLLFLDEPTTGLDPRSRNQVWDIVRAVVAQGTTVLLTTQYLDEADQLAARIAVIDKGRVIAEGTKGELKASVGAGSVHVRLRDAAQRAEAAQLLEHALAAQVQLEPDPVALTARVGDGGRHAEEAAAEKASRALAGLARAGIVVDNFSLGQPSLDEVFLALTDQPLDHHRQNGTQQDRTQQDRKEAEAAL
>NZ_CP023690.1|WP_150512143.1|5105525_5106371_-|ABC-transporter-permease
MSTVTTVEAQDLAPVRTESLAELLISKERPRRPSALSTSLTFGWRAVLKIKHVPEQLFDVTAFPIMMVLMYTYLFGGALAGSPREYIQYLLPGILVMSVVMITMYTGVSVNTDIEKGVFDRFRSLPIWRPSAMVGYLLGDVLRYAMASAVMLSVGLILGFRPDNTVGVLLGVLLLLVFSFAFSWVWTMFGLLLRTEKSVMGVSMMVLFPLTFLSDIFVKPETMPGWLQAFVNNNPVTHVASAVRGLMAGDWPGTEIAWSLGWAALLVAVFGPVTMRLYNRK
>NZ_CP023690.1|WP_150515634.1|5104574_5105405_-|hypothetical-protein
MLLVLSCLLVPLGVVSTWAAYEIQDTDRYVATMAPLSSDPAVRAAVADAVTDSVVKEIDAGPLQSTVESFVRDAVRSFTGTAAFRTAWNAANRAAHAAVEQALENDSEGEVTIDLAPITQQVKRQLSEEGVPFADRIPVRHTEVTVMKAQDLSDYRKVFRMLQAAGLWLPVAAAVFAVGGILLAAHRRHAVLATALGTAAGAAALAAAVAVGRALTLDDLPPDVSRAAAGAVYDALTRTLWVTAWVLVGLGLLVAAGMWWLSHRRAGKLSVEPPRL
>NZ_CP023690.1|WP_150512142.1|5103500_5104517_-|endonuclease/exonuclease/phosphatase-family-protein
MEHATAPPTAPEDAFPADVPVRRPGRWRLAAWTAGLLLAGVSAVLGCRAADTDAFTPVPQVLAFLPWLLAPAALALLLAAYGRWRVGLVWAVAVLGGLAWFMEPYGKVAEPDGPPLADLRVLASNVEFGRGAPGLVKAVREHEPDLVFVSECDRACQDTLREELPDSAYPYRVAAGGNGADGSVILANVPLKRAAGVRGTLGMPGAVADVKGVAVRLQLAHPMPPTPGDVDRWRAELGSLRAYAAAGDGRPTILAGDFNATQDHAAFRHILDTGLRDGARVAGASRTPTWPTALPRPFGAQIDHVLTTPDFAAHEARFLTIGNTDHRAVLLDLTLHRG
>NZ_CP023690.1|WP_150512149.1|5114884_5115208_+|TfoX/Sxy-family-protein
MAYDEVLADRIRERLEPEGVTAKKMFGGITFLLQGNALANLYEEGLMVRVGPEGMEEALGRPGARQFVFRGKEQNGWVVLAEETLDDEVLDDWLKWAMEVTAELPPK
>NZ_CP023690.1|WP_150512150.1|5115242_5115719_+|NUDIX-domain-containing-protein
MSFRLAAYAVCVEGGRVLLARHVSRKGESTWTLPGGRVEHAEDPFDAVVREVAEETGCDAVVERLLGVDSRVIPAAERAVPGELDHQNVGVFYQVRITGGQPRPEPDGGGIAESVWTPLPDVAGLCRSSLVDVGLALARTRPPTGHVATVPVGGLIRH
>NZ_CP023690.1|WP_150512151.1|5115803_5116214_+|VOC-family-protein
MDITIHTTALPHDDPDASLAFYRDVLGFEVRGDVGQGRMRWITVGPAGQPGTSILLAPPAADPGITEDERRTITEMMAKGTYGWILLATRDLDATFERVQAGDTEVVQEPTEQPYGVRDCAFRDPAGNLVRIQELR
>NZ_CP023690.1|WP_150512152.1|5116541_5117378_-|glucose-1-dehydrogenase
MRTRWRPRIRARRRESGSCAVTDPELPSLEGRVALVTGASGLLGGGIARRFAAAGAAVVLHCREQGERARELAEEIGEAGGDALVVAADLREEDECRRLIGAARDWRGRLDALVNNAGVQPVQPLPGMTAADWRELQEANVTSAFACTQAAAEVMGAQDGGGSVTQIASIEGHQPAPGHAHYASSKAALIMFARAAAVEYGAAGVRVNSVSPGLIGRPGLAEDWPEGVERWGRAAPLSRLGRAEDVGSACVFLASPAASWITGVDLVVDGGVSARPTW
>NZ_CP023690.1|WP_150512153.1|5117310_5117781_-|cupin-domain-containing-protein
MTPEELIAEHGLVPLEFEGGRFRRTWAGPPDAAGRPVGTAIIMLLTAEPGDFSALHRLPIDEVWHFYRGDALELLLLHPDGSDEVRVLGPGDGEFQTVVPAGAWMGARVRDGGAWALFGTTMAPGFIDEDFEGGDADALAAAYPRQATRIRELCRD
>NZ_CP023690.1|WP_150515636.1|5117770_5118166_-|ATP-binding-protein
MSFTVGEHSARPLRRILRLYLGSWGLAGLADEAELALTELVANVVRHVPDRRCAVLLLRRPRGLRVEVTDGSPALPAPADGGPAGEPAEGGYGLRLVDAVTDRWDVTVLPGGAGKTIWFECDDGKDVDGDP
>NZ_CP023690.1|WP_150512154.1|5118215_5119151_+|helix-turn-helix-domain-containing-protein
MSLRLTRCAYPWLRNESNADERLTLGVNPPVVRINELDPSASPLDYYGSELRRLREAAGLNQAELGGCIFCTGSLVGQIETAKKVPTRDFSERLDAALGTDGAFSRLVGLVLRSQLPSWFQAFAEMEAKATYISTYQAQLIYGLLQTKEYARAVLATGMPNNLDDLVAARMERQRILTRERPPLALVILDEATLHRPIGGREVMRGQLAHLLKCAERRWVRIQVLPYSAGEHASLIGSFTALRFEDDPDLVYTEDLISGHMTANPETVREAAFRYANLQAAALSVEESAGLITRVMEERYGLPGPDERAVA
>NZ_CP023690.1|WP_150512155.1|5119113_5119374_+|DUF397-domain-containing-protein
MGYQDLTNARWRRSSYSGNTGGECVECAPLDGAAWRKSSHSGSTGGDCLEVTELPGPHIAIRDSKRPAGPHLTVSAAAFTALVSTL
>NZ_CP023690.1|WP_150512156.1|5119498_5120092_+|DUF4291-family-protein
MEHPKHQIRAAHTDTTVTVYQAYAPHIGEPTARNGRFPAAWRRERMTWIKPSFLWMMYRCGWGTKEGQETVLALEISREGFDWALAHACLSHYEPGVHADAADWKRQLKQAPARVQWDPERDLHLRPLPHRSLQLGLAGEASRRYADEWIVSVTDVTERARRVRELVAAGALDRARTLLPTEPVYPAGDALLTHLRP
>NZ_CP023690.1|WP_150515637.1|5120178_5120862_-|TetR/AcrR-family-transcriptional-regulator
MTDEPGGAARRPARAYGGKSAEQRRADRRRRLLEAGVDLFGAGPGAYRSASVAALCARAGLSTRQFYEEFRNLEEVLAALHRHVQKAAQGAVVEALAEAAGGTVRERVESAFRAYARVLTAHPHLVRIAFVEVTGVTPELERQRLEARKGWVGLLVAALDEAVERGEIGARDYRVAALGFVGAVNALLYDWTAGYVDADLDTIVEELMRMFMGLLQPPSAEGSAPGC

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Crispr_ID: NZ_CP023690_8

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_8

5545814-5546505

Orphan

I-C,I-E,II-B:NA

Consensus_repeat	Method
CCCCGCACGCGCGGGGACCAC	CRT
GGGACCACCCCCGCACGCGCGGGGACCAC	CRISPRCasFinder
GGGTGGTCCCCGCGCGTGCGGGGGTGGTCCCGT	PILER-CR
GTGGTCCCCGCGCGTGCGGGGATGGTCCC	PILER-CR

11 spacers

The CRISPR arrays of NZ_CP023690_8

>merge|NZ_CP023690|8|5545814-5546505|CRT,CRISPRCasFinder,PILER-CR,PILER-CR
CCGCGTATGCGTGGGAGCCACTTCAACCTCGGCCAGGGGGGAGAGGCCACTATGGGTCCATCCCCGCACGCGCGGGGACCACCCGGGGGAGGAGTACTCGCCGCCGACCTGCCCGGGACCACCCCCGCACGCGCGGGGACCACCCTTCCCGGAGCGCGAGCACCTGGGGGATCAGGGGACCACCCCCGCCCGCGCGGGGACCACCCCGGCAGTCACTTCGCGGTCTGCGGCCAGATGGGACCACCCCCGCACGCGCGGGGACCACGCGTACCCCAGCAGCGGCCAGTGGCAGGTCGAGGGACCACCCCCGCACGCGCGGGGACCACATGAGCCTGAACCCGATCGAGGAGGGCGAGGAGGGACCACTCCCGCACGCGCGGGGATCACCTGAACTGCTCGCGGGCTGCATGCGCTCGGCTGGGACCATCCCCGCACGCGCGGGGACCACAGCGCACACCCCGTGGCTGAGCTGCGGGTCCAGGGACCATCCCCGCACGCGCGGGGACCACCAGCACACGCTTCACCGCGTCCTGCTCGCCGCAGGACCATCCCCGCACGCGCGGGGACCACGAGGTGCAGTATCCGTACGGCATCCCCGTGATGGGACCACCCCCGCACGCGCGGGGACCACACCTGGCCTGTGACGTTCACGGGCAAGCCGGGGGGACCACCCCCGCACGCGCGGGGACCAC

>NZ_CP023690|8|3|5545814-5546505|CRT
CCGCGTATGCGTGGGAGCCAC	TTCAACCTCGGCCAGGGGGGAGAGGCCACTATGGGTCCAT
CCCCGCACGCGCGGGGACCAC	CCGGGGGAGGAGTACTCGCCGCCGACCTGCCCGGGACCAC
CCCCGCACGCGCGGGGACCAC	CCTTCCCGGAGCGCGAGCACCTGGGGGATCAGGGGACCAC
CCCCGCCCGCGCGGGGACCAC	CCCGGCAGTCACTTCGCGGTCTGCGGCCAGATGGGACCAC
CCCCGCACGCGCGGGGACCAC	GCGTACCCCAGCAGCGGCCAGTGGCAGGTCGAGGGACCAC
CCCCGCACGCGCGGGGACCAC	ATGAGCCTGAACCCGATCGAGGAGGGCGAGGAGGGACCAC
TCCCGCACGCGCGGGGATCAC	CTGAACTGCTCGCGGGCTGCATGCGCTCGGCTGGGACCAT
CCCCGCACGCGCGGGGACCAC	AGCGCACACCCCGTGGCTGAGCTGCGGGTCCAGGGACCAT
CCCCGCACGCGCGGGGACCAC	CAGCACACGCTTCACCGCGTCCTGCTCGCCGCAGGACCAT
CCCCGCACGCGCGGGGACCAC	GAGGTGCAGTATCCGTACGGCATCCCCGTGATGGGACCAC
CCCCGCACGCGCGGGGACCAC	ACCTGGCCTGTGACGTTCACGGGCAAGCCGGGGGGACCAC
CCCCGCACGCGCGGGGACCAC

>NZ_CP023690|8|8|5545867-5546505|CRISPRCasFinder
GGGTCCATCCCCGCACGCGCGGGGACCAC	CCGGGGGAGGAGTACTCGCCGCCGACCTGCCC
GGGACCACCCCCGCACGCGCGGGGACCAC	CCTTCCCGGAGCGCGAGCACCTGGGGGATCAG
GGGACCACCCCCGCCCGCGCGGGGACCAC	CCCGGCAGTCACTTCGCGGTCTGCGGCCAGAT
GGGACCACCCCCGCACGCGCGGGGACCAC	GCGTACCCCAGCAGCGGCCAGTGGCAGGTCGA
GGGACCACCCCCGCACGCGCGGGGACCAC	ATGAGCCTGAACCCGATCGAGGAGGGCGAGGA
GGGACCACTCCCGCACGCGCGGGGATCAC	CTGAACTGCTCGCGGGCTGCATGCGCTCGGCT
GGGACCATCCCCGCACGCGCGGGGACCAC	AGCGCACACCCCGTGGCTGAGCTGCGGGTCCA
GGGACCATCCCCGCACGCGCGGGGACCAC	CAGCACACGCTTCACCGCGTCCTGCTCGCCGC
AGGACCATCCCCGCACGCGCGGGGACCAC	GAGGTGCAGTATCCGTACGGCATCCCCGTGAT
GGGACCACCCCCGCACGCGCGGGGACCAC	ACCTGGCCTGTGACGTTCACGGGCAAGCCGGG
GGGACCACCCCCGCACGCGCGGGGACCAC

>NZ_CP023690|8|3|5545927-5546080|PILER-CR
CGGGACCACCCCCGCACGCGCGGGGACCACCCT	TCCCGGAGCGCGAGCACCTGGGGGATCA
GGGGACCACCCCCGCCCGCGCGGGGACCACCCC	GGCAGTCACTTCGCGGTCTGCGGCCAGA
TGGGACCACCCCCGCACGCGCGGGGACCACGCGTACCCCAGCAGCGGCCAGTGGCAGGTCGAGGGACCACCCCCGCACGCGCGGGGACCACATGAGCCTGAACCCGATCGAGGAGGGCGAGGAGGGACCACTCCCGCACGCGCGGGGATCACCTGAACTGCTCGCGGGCTGCATGCGCTCGGCTGGGACCATCCCCGCACGCGCGGGGACCAC	AGCGCACACCCCGTGGCTGAGCTGCGGGTCCA
GGGACCATCCCCGCACGCGCGGGGACCAC	CAGCACACGCTTCACCGCGTCCTGCTCGCCGC
AGGACCATCCCCGCACGCGCGGGGACCAC	GAGGTGCAGTATCCGTACGGCATCCCCGTGAT
GGGACCACCCCCGCACGCGCGGGGACCAC	ACCTGGCCTGTGACGTTCACGGGCAAGCCGGG


>NZ_CP023690|8|4|5546233-5546505|PILER-CR
	TCCCGGAGCGCGAGCACCTGGGGGATCA
GGGGACCACCCCCGCCCGCGCGGGGACCACCCC	GGCAGTCACTTCGCGGTCTGCGGCCAGA
TGGGACCACCCCCGCACGCGCGGGGACCACGCGTACCCCAGCAGCGGCCAGTGGCAGGTCGAGGGACCACCCCCGCACGCGCGGGGACCACATGAGCCTGAACCCGATCGAGGAGGGCGAGGAGGGACCACTCCCGCACGCGCGGGGATCACCTGAACTGCTCGCGGGCTGCATGCGCTCGGCTGGGACCATCCCCGCACGCGCGGGGACCAC	AGCGCACACCCCGTGGCTGAGCTGCGGGTCCA
GGGACCATCCCCGCACGCGCGGGGACCAC	CAGCACACGCTTCACCGCGTCCTGCTCGCCGC
AGGACCATCCCCGCACGCGCGGGGACCAC	GAGGTGCAGTATCCGTACGGCATCCCCGTGAT
GGGACCACCCCCGCACGCGCGGGGACCAC	ACCTGGCCTGTGACGTTCACGGGCAAGCCGGG
GGGACCACCCCCGCACGCGCGGGGACCAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150512458.1\|5556934_5557189_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512445.1\|5536078_5536381_-\|PLDc-N-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|379161
NZ_CP023690.1\|WP_144320328.1\|5540320_5541484_+\|aminofutalosine-synthase-MqnE	unknown	unknown	gnl\|CDD\|213851
NZ_CP023690.1\|WP_150512450.1\|5544800_5545718_+\|phosphotransferase	unknown	unknown	gnl\|CDD\|366736
NZ_CP023690.1\|WP_150512457.1\|5556264_5556756_-\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380345
NZ_CP023690.1\|WP_150512459.1\|5557175_5557424_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512447.1\|5537917_5538820_+\|4-hydroxybenzoate-octaprenyltransferase	unknown	unknown	gnl\|CDD\|183814
NZ_CP023690.1\|WP_150512456.1\|5554853_5556251_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP023690.1\|WP_150515676.1\|5549013_5549631_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP023690.1\|WP_150512454.1\|5552123_5553704_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|312032
NZ_CP023690.1\|WP_150512452.1\|5549616_5550465_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366711
NZ_CP023690.1\|WP_030685400.1\|5539811_5540267_+\|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|214628
NZ_CP023690.1\|WP_150512455.1\|5553717_5554587_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|375319
NZ_CP023690.1\|WP_150512451.1\|5548319_5548766_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP023690.1\|WP_150512448.1\|5538816_5539530_+\|UbiX-family-flavin-prenyltransferase	unknown	unknown	gnl\|CDD\|223241
NZ_CP023690.1\|WP_150512449.1\|5541590_5541881_+\|DUF4229-domain-containing-protein	unknown	unknown	gnl\|CDD\|379415
NZ_CP023690.1\|WP_150512444.1\|5535040_5535961_-\|isopenicillin-N-synthase-family-oxygenase	unknown	unknown	gnl\|CDD\|226022
NZ_CP023690.1\|WP_150512453.1\|5550527_5551841_-\|3-oxoacyl-ACP-reductase	unknown	unknown	gnl\|CDD\|236207
NZ_CP023690.1\|WP_150512446.1\|5536469_5537921_+\|menaquinone-biosynthesis-decarboxylase	unknown	unknown	gnl\|CDD\|163413
NZ_CP023690.1\|WP_150515675.1\|5542272_5543604_+\|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl\|CDD\|224220

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150512445.1\|5536078_5536381_-\|PLDc-N-terminal-domain-containing-protein	gnl\|CDD\|379161	pfam13396, PLDc_N, Phospholipase_D-nuclease N-terminal. This family is often found at the very N-terminus of proteins from the phospholipase_D-nuclease family, PLDc, pfam00614. However, a large number of members are full-length within this family.	0.000438116
NZ_CP023690.1\|WP_144320328.1\|5540320_5541484_+\|aminofutalosine-synthase-MqnE	gnl\|CDD\|213851	TIGR03700, mena_SCO4494, putative menaquinone biosynthesis radical SAM enzyme, SCO4494 family. Members of this protein family appear to be involved in menaquinone biosynthesis by an alternate pathway via futalosine, based on close phylogenetic correlation with known markers of the futalosine pathway, gene clustering in many organisms, and paralogy with the SCO4550 protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP023690.1\|WP_150512450.1\|5544800_5545718_+\|phosphotransferase	gnl\|CDD\|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	2.08138e-17
NZ_CP023690.1\|WP_150512457.1\|5556264_5556756_-\|cupin-domain-containing-protein	gnl\|CDD\|380345	cd02215, cupin_QDO_N_C, quercetinase, N- and C-terminal cupin domains. This family contains quercetinase (also known as quercetin 2,3-dioxygenase, 2,3QD, QDO and YxaG; EC 1.13.11.24), a mononuclear copper-dependent dioxygenase that catalyzes the cleavage of the flavonol quercetin (5,7,3',4'-tetrahydroxyflavonol) heterocyclic ring to produce 2-protocatechuoyl-phloroglucinol carboxylic acid and carbon monoxide. Bacillus subtilis quercetin 2,3-dioxygenase (QDO) is a homodimer that shows oxygenase activity with several divalent metals such as Mn2+, Co2+, Fe2+, and Cu2+, although the preferred one appears to be Mn2+. The dioxygen binds to the metal ion of the Cu-QDO-quercetin complex, yielding a Cu2+-superoxo quercetin radical intermediate, which then forms a Cu2+-alkylperoxo complex which then evolves into endoperoxide intermediate that decomposes to the product. Quercetinase is a bicupin with two tandem cupin beta-barrel domains, both of which are included in this alignment model. The pirins, which also belong to the cupin domain family, have been shown to catalyze a reaction involving quercetin and may have a function similar to that of quercetinase.	5.78665e-16
NZ_CP023690.1\|WP_150512447.1\|5537917_5538820_+\|4-hydroxybenzoate-octaprenyltransferase	gnl\|CDD\|183814	PRK12888, ubiA, 4-hydroxybenzoate octaprenyltransferase.	1.68465e-172
NZ_CP023690.1\|WP_150512456.1\|5554853_5556251_+\|MFS-transporter	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	6.96803e-58
NZ_CP023690.1\|WP_150515676.1\|5549013_5549631_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.7487e-14
NZ_CP023690.1\|WP_150512454.1\|5552123_5553704_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|312032	pfam08386, Abhydrolase_4, TAP-like protein. This is a family of putative bacterial peptidases and hydrolases that bear similarity to a tripeptidyl aminopeptidase isolated from Streptomyces lividans. A member of this family is thought to be involved in the C-terminal processing of propionicin F, a bacteriocidin characterized from Propionibacterium freudenreichii.	7.15779e-25
NZ_CP023690.1\|WP_150512452.1\|5549616_5550465_-\|hypothetical-protein	gnl\|CDD\|366711	pfam01575, MaoC_dehydratas, MaoC like domain. The maoC gene is part of a operon with maoA which is involved in the synthesis of monoamine oxidase. The MaoC protein is found to share similarity with a wide variety of enzymes; estradiol 17 beta-dehydrogenase 4, peroxisomal hydratase-dehydrogenase-epimerase, fatty acid synthase beta subunit. Several bacterial proteins that are composed solely of this domain have (R)-specific enoyl-CoA hydratase activity. This domain is also present in the NodN nodulation protein N.	1.04851e-13
NZ_CP023690.1\|WP_030685400.1\|5539811_5540267_+\|Lrp/AsnC-family-transcriptional-regulator	gnl\|CDD\|214628	smart00344, HTH_ASNC, helix_turn_helix ASNC type. AsnC: an autogenously regulated activator of asparagine synthetase A transcription in Escherichia coli).	2.20402e-35
NZ_CP023690.1\|WP_150512455.1\|5553717_5554587_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|375319	pfam17765, MLTR_LBD, MmyB-like transcription regulator ligand binding domain. This domain is found in a family of actinobacterial transcription factors. The structure shows it has a PAS domain like fold and it is bound to Myristic acid.	6.42908e-57
NZ_CP023690.1\|WP_150512451.1\|5548319_5548766_+\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.508e-08
NZ_CP023690.1\|WP_150512448.1\|5538816_5539530_+\|UbiX-family-flavin-prenyltransferase	gnl\|CDD\|223241	COG0163, UbiX family flavin prenyltransferase [Coenzyme transport and metabolism].	4.3712e-65
NZ_CP023690.1\|WP_150512449.1\|5541590_5541881_+\|DUF4229-domain-containing-protein	gnl\|CDD\|379415	pfam14012, DUF4229, Protein of unknown function (DUF4229). This family of integral membrane proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 95 and 122 amino acids in length.	7.86191e-16
NZ_CP023690.1\|WP_150512444.1\|5535040_5535961_-\|isopenicillin-N-synthase-family-oxygenase	gnl\|CDD\|226022	COG3491, PcbC, Isopenicillin N synthase and related dioxygenases [General function prediction only].	9.87049e-54
NZ_CP023690.1\|WP_150512453.1\|5550527_5551841_-\|3-oxoacyl-ACP-reductase	gnl\|CDD\|236207	PRK08261, fabG, 3-ketoacyl-(acyl-carrier-protein) reductase; Provisional.	0
NZ_CP023690.1\|WP_150512446.1\|5536469_5537921_+\|menaquinone-biosynthesis-decarboxylase	gnl\|CDD\|163413	TIGR03701, mena_SCO4490, menaquinone biosynthesis decarboxylase, SCO4490 family. Members of this protein family are putative decarboxylases involved in a late stage of the alternative pathway for menaquinone, via futalosine, as in Streptomyces coelicolor and Helicobacter pylori. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP023690.1\|WP_150515675.1\|5542272_5543604_+\|cation:dicarboxylase-symporter-family-transporter	gnl\|CDD\|224220	COG1301, GltP, Na+/H+-dicarboxylate symporters [Energy production and conversion].	6.99917e-112

>NZ_CP023690.1|WP_150512450.1|5544800_5545718_+|phosphotransferase
MAADAGQGSEKGFMEAGATRVMTAACRAAGLDDRDAELIRLGENALFRLASAPVIVRVARGPEWLTKARNEVAVSRWLTGEGFPATRAVEDLEQPLVIDGHPVTFWHLIVEADRKATYGELGGVLRDLHSMTVPEGLHLPSYEPFDKSDVRLDKAVIPDDDKAFLRKRARELRDKCAELRFETPKGPVHGDAHVQNLMVDVQGRVILIDFEVFCFDHPEWDLMVTSVEHHSLGWQTEQQYADFVGAYGRDLYDWEGYATLRGLQEFNMTTWLMQNVRVSERVADEYRRRIAALRDDDGPRDWRPW
>NZ_CP023690.1|WP_150515675.1|5542272_5543604_+|cation:dicarboxylase-symporter-family-transporter
MSANSATPAGEPKPGFRIPKFLKLPFWAQILGGLVLGVLLGWLARSQDISWLVTTLSKVGDTFIGLLKLAVAPLVFFAILISITNLRKVNNAARLATRTLLWFMITSLIAVVIGLVIGLVTNPGAGTGLTPKDGAKPEHEGSWIDFLTGIIPTDVITPFTELNVLQIVFMAAVAGVAILKIGDEKAKPILDLSESILTLLQKALWWVIKLSPIGTIGLIGFAIADYGWNLISKYATFTADIYIGCALVMFGVYPLLLATVAKVSPLQFFKGAWPAIQLAFVSRSSVGTMPLTQKVTERLGVPKEYTSFAVPFGATTKMDGCAAIYPAIAAIFVAQIFDVNMGIKEYLLIAFVSVVGSAATAGLTGATVMLTLTLSTLGLPMEGVGLLLAIDPVLDMMRTATNVAGQALVPVLVAARENILDREAYEHASASPIDEPDVVPANA
>NZ_CP023690.1|WP_150512449.1|5541590_5541881_+|DUF4229-domain-containing-protein
MLRYTLMRLGVFAGCFLVVWGLVYSGIVPRGLGGSNLLWVALLSLVVSAPLSFVLLRKERDRASEKVVAKVDNVKASLERNRTQEDGADDATRTAQ
>NZ_CP023690.1|WP_144320328.1|5540320_5541484_+|aminofutalosine-synthase-MqnE
MDAGLKRDLEEKVRSGERLSREDGIALYESDDLAWLGGLAHEVRTRKNGDVVHFNVNRHLNMTNVCTASCAYCSFQRKPGEKDAYTMRIEEAVRLAKAMEADNLTELHIVNGLHPNLPWRYYPRSLRELKAALPNVSLKAFTATEIHHFETISGLSASEILDELIDAGLESLTGGGAEIFDWEVRQHIVDHKTHWEDWSRIHRLAHEKGLKTPATMLYGHIEEPRHRVDHVLRLRELQDETGGFQVFIPLRYQHDFVDMQDGKVRNRLQARTKMASGIEALKTFAVSRLLFDNVPHVKVFWVMHGLATAQLALQHGADDMDGSVVEYKITHDADNFGTPNKLTRDDLLDLIREAGFRPVERNTRYEVIREFPGPDRELRESPQPMRL
>NZ_CP023690.1|WP_030685400.1|5539811_5540267_+|Lrp/AsnC-family-transcriptional-regulator
MDAVDRQLIQALRENGRASYAELGRLVGLSGPSVTDRINRLEAAGVITGYRATVDSASLGLGVTALIGISLSDAADHEDVARRLRDLHEIEDCWFIAGDDSYMLKVRASDVDGLEKTIRRLSGTKGVSRTRTTIVLSTKWENRVGELPEEV
>NZ_CP023690.1|WP_150512448.1|5538816_5539530_+|UbiX-family-flavin-prenyltransferase
MTGRTEPVDRLRGVNAGDTERRPWVVGVSGASGTPYAAAVLRALLAAGESVDLVVSRASRLTLLDETGISFRDAHWRADLEQWLARGADGKPDTFRVRTDDVRYWAAGDLAAGPSSGSYATKGMLIVPASTACVAGVALGLSKDLLQRVASVTLKEGRRLVVCVRETPLNGQTLRHLVSLDEAGAIVLPASPAFYAGATHIQDLVDFVAGRMLDAAQVPHRLYRRWEGELGGGSREG
>NZ_CP023690.1|WP_150512447.1|5537917_5538820_+|4-hydroxybenzoate-octaprenyltransferase
MSSASAALPQPGRTKAFLRLVMIEHSVFALPFAYIASLTAMYEWDKNIHWGRLLLVTICMVGLRTFAMAANRIIDREIDARNPRTAHRELVTGAVTVKSAWTGALVAVVVFLGSAALLNPLCLALAPVAVIPMVVYPYGKRFTNFPQAILGIAQAMGPIGAWLAITGEWSWTAVILGLAVGVWIGGFDLIYACQDVESDREAGVLSVPARFGVPASIRGARGCHAVTTALLVWYAVQTGAGAFFWLGLLIVAGAFLYEHSIVRPHDLSRLNRAFFQVNGFIGIALFVCALLDLLVRGLTV
>NZ_CP023690.1|WP_150512446.1|5536469_5537921_+|menaquinone-biosynthesis-decarboxylase
MAYDDLRSLLRALEREGDLKRIKAEVDPYLEVGEIVDRVQKSGGPALLFENVKGSDMPLAMNVFGTDRRLLKALGLKSYGEISEKIGGLLRPELPQGFVGVREAFGKLGAMTHVPPKKVKDAPVQEVVLRGEDVDLDRLPALFTWPKDGGSFFNLGLTHTKDPESGVRNLGLYRLQRHDRRTIGMHWQIHKDSRNHYQVAARRGERLPVAIAFGCPPAVTYASTAPLPGDIDEYLFAGFLQGKRIEMVDCKTVPLQVPAQAEVVLEGWLEPGEMLPEGPFGDHTGFYTPQEPFPALTIDCVTMRKRPLLQSIVVGRPPTEDGPLGRATERFFLPLLKIIVPDIVDYHLPESGGFHNCAIVSIDKKYPKHAQKVMHAIWGAHMMSLTKLIVVVDSDCDVHDLHEVSWRALGNTDYARDLTVVEGPVDHLDHASYQQFWGGKAGIDATKKWPEEGYTRDGGWPDMVESDPDTAALVDRRWREYGL
>NZ_CP023690.1|WP_150512445.1|5536078_5536381_-|PLDc-N-terminal-domain-containing-protein
MLRYLPFLLVLAVWIYAFIDVLNTPEKEVRHLPKVVWVIIVLLFGEVLLGPIAWFVTGKKRGPATGRAGGSRGGWVAPDDNPEFLKNLNKDLDDKRDEGK
>NZ_CP023690.1|WP_150512444.1|5535040_5535961_-|isopenicillin-N-synthase-family-oxygenase
MTIPTVDLRAWRSGPPEARQEIKRAVDDGLRTAGFLLVTGHDVAPGLRTAIREESRSFFRLPPEAKQPYSVRVGARGWLGPGAEANSYAEGTPSPPDLKESLSFAADEPTGDAAVDAEWFAPNTWPAETPGLRACVETYLRLMRTLSDQLLELLAAALGEPEDFFTRHTGHPTWGFNINWYPGRDRVGTPEPGQFRIGPHTDFGTVTVLDRQAGRGGLQVFTDADGWQDAPWDPEAFTINIGDLMARWTGGRWRSGRHRVLPPPADVPAEELMSLVYFYECDPGTDVRGIDSHVYLRAQLDAIASG
>NZ_CP023690.1|WP_150512451.1|5548319_5548766_+|ATP-binding-protein
MGARPSKNRANTSGMAAPRADAADSSAGHHRALTLSADSRDAVRAAREMVRGSLQDWGLERIGDDARLAVSELVSNVVQHAVPDNCLAQPGARRRIDISVMTWPGLLCIGVTDEDSAPPDLPVGDRLSPELAGDFPEALLPERGRGLS
>NZ_CP023690.1|WP_150515676.1|5549013_5549631_+|TetR-family-transcriptional-regulator
MPRAVRERQMLDAAVRTFGQRGYRAASMDEIAELAGVSKPLVYLYLNSKEDLFTACIRREAAALTQAVRSAVNPDAPADQQLWDGLRAFFEHTALHPDAWAVLHSQARTVGEPFAAEVNAARAEIVAFVTALIGAAARAAHRDPSLPDREVAGLAHALVGAAESLAGWANTEPSVPAKEAAATLMNFAWAGLGDLMEGRPWSPPA
>NZ_CP023690.1|WP_150512452.1|5549616_5550465_-|hypothetical-protein
MPRPPLPLTLLKGAFLSPLKHPGTGHGNGGPRLRDRARATPGRADAYRRVCGFAPTGEPPGDTLPLPYPHVLAFPLTTRLMAARAFPLPLLGLVHTSIEVVRHRALRPTDDLGLTAYVEKLAPHRRGTEATLTVEATVDGTIAWESRSTYLARHETGATAPPRQGPGDEPPLPVEARWRLAAGLGRRYAAVSGDRNPIHLHPLTARPFGFPRPIAHGMWTFARCLAEYGPTGTEPVRVTARFRAPVLLPATVTYGRRGQHFELRDSTGRPHVRGRVEPLGGR
>NZ_CP023690.1|WP_150512453.1|5550527_5551841_-|3-oxoacyl-ACP-reductase
MADRYLTFTRTAPGRFLTRRLGLPRPVPLRRFSPEHPALDGPLLHLTAGDLPLPGLHEVLTRTGLPPHTGPLGTRHPAAVVLDATGVATVSALVDVHATLHPVVRSIADCGRVVVLGAPLSPADHHQAAAQQALDGFVRSLAKELGRGRTATLVRTASAPATEPTLRFLLSPKSAYVNGQTIEVTPDAHAPENDSPGRPLAGRTALVTGAARGIGAAVAEVLARDGARVVALDVPAARTDLVRVAERVGGAPLALDITADDAGERIAAALPGGLDVLVHNAGITRDRRLANMAADRWSSVLDVNLGSVLRTTDFLLKSGTLRRGGSVVATASVAGLAGNAGQTNYAASKAGVAGLVRSLAPRALAEHGITVNAVAPGFIETRMTAAVPLLIREAGRRLNSLAQGGQPVDVAETVAWLALGGVNAQVIRVCGQSLLGA
>NZ_CP023690.1|WP_150512454.1|5552123_5553704_+|alpha/beta-fold-hydrolase
MEAAVRTPALTGVTALALALTALPAATGAEPPRPDLKRFYAQKVKWAVCTPEKQNLPETVTKNEDVRCGTLTVPLDYARPRSGTVDLALLKVKASGKKRGSLLVNFGGPGGPGVAGLAADLKGFGDLGKGYDVVGFDPRGVGLSEPVSCGDEPEPEGLDDPDDAGAVLEQLRRTAERCVKESGPVLPHIGTVNVSRDMDVMRAALGDKKLNYLGFSYGTRLGAVYAAQFPKKVGRMVLDGVDTLTEPVDEQGLASAEGQQTALDNFLLWCTKNAGCVFGDDSRRARETMVKVIEDLDAMPLRSTDGAEFTGQDVVSVLGSALYSRQAWPALSQALGALLADGDPRALMRVGGAGGMGVGHGFGRGFGHGFGHGRQDVPQDNETAALAAVNCADDPDRPGARKVEKEIGRLQQEFEEVSPVFGEHNLTLVLMCFGWPAGTSYIRKEVRDVDTPKLLLVGTRGDPATPYRWTEETARRLGSSAVVLDNKGDGHTGYFGSKCVKAKVDGFLLYKQLPANGSSCAAEWRE
>NZ_CP023690.1|WP_150512455.1|5553717_5554587_-|helix-turn-helix-domain-containing-protein
MKSNGGTELGRYLRARRAQIRPEDTGLPAGTGIRRTPGLRREELATLAGVSVDYYTRLERGRESNPSPAVVDALARALHLRGDAHERLHELAELASGRLTEPRPTAEFTVRESVHRMLEALRPLPAYVVGPYSDMLAANAPCRRLMPGLWDWPAQERNLVRYLFLHPVGRTLYVPWEETVALSIAHLRAVGGRDPDSPRLTALVGELMLKSPDFARLWDRYEVCERGGGVKSFAHPKVGPMTLTYEVMSLARTGGQRLVTYQAEPGSADEAAMLRLDSASRTAAEPSTR
>NZ_CP023690.1|WP_150512456.1|5554853_5556251_+|MFS-transporter
MPLTLQAPAPPRPTPRAATALLASLLGFTVITVDVSAVNIALPDIRSSLHGGMTGLQWVVDAYTLMFAALMISAGALADRAGARRAYAWGTALFTLASLACALAPGIGALIAARVGQGAAAAVVMPASLALIRQAYDDPRQRARAIALWTVGGSAAMAAGPVLGGVLTQTVGWRAVFLLNLPIGALILALLTRTAPSPRRPAPLDVPGQLTAVLGLGALAYAVIEGGHAGPTSPSVLVAAGLAVAAVFAFRAAERRHPAPMVPLPLLRQREVGVSLAVGFAVNAGFYGVVFLLGLYLQQLRGMSAVAAGLTFVPLAVLITSTNLVSPRFAERAGRRPVIVTGQLILAVAMFALLPLAADTPMWLVLVLLVPTGIGGALAVPALTALLMDAVPGHRAGTASGLLNSLRQTGGALSVALFGALIGSGGGYSVGGMRQGLVVVGLVLLGTAALSVWRLPRGVPRGGGR
>NZ_CP023690.1|WP_150512457.1|5556264_5556756_-|cupin-domain-containing-protein
MSYPDPRYFSDKGEVSAVFRPADTPPDHSTPTQDYHYLATTVVTQGEFGLYKVDMGPRAGGPTTHFHKGISESFYVLDGELELYDGDRWRTGGPGDFLYVPVGGLHAFRNASDAPTSMLMLFAPGAPREEYFENVAEMARRGGDEFGRFLVEHDSFFVDQGYR
>NZ_CP023690.1|WP_150512458.1|5556934_5557189_-|hypothetical-protein
MAGSDTDGIALELERLHRSVDVGFATTRGDLALLLQRADQTDKALSEHEERLDALERTRWPLPSLAAVTSCTALALTLWQQSGR
>NZ_CP023690.1|WP_150512459.1|5557175_5557424_-|hypothetical-protein
MNDTGRRALRTLVQTLFGLVTALPLLADDPAARGLPGIAVAVAVAGALSRLMSAPAVERLLPAWLRVRTGPPPGEEADHGRL

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Crispr_ID: NZ_CP023690_7

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_7

5543678-5544438

Orphan

Consensus_repeat	Method
GGGACCACCCCCGCACGCGCGGGGACCAC	CRT
GGGACCACCCCCGCACGCGCGGGGACCAC	CRISPRCasFinder
GTGGTCCCCGCGCGTGCGGGGGTGGTCCC	PILER-CR

12 spacers

The CRISPR arrays of NZ_CP023690_7

>merge|NZ_CP023690|7|5543678-5544438|CRT,CRISPRCasFinder,PILER-CR
CTTGGGGGGCCCGTATGCGCGGGGACCACGAGTCGGGTTCGCTGTGCTCGCCGCTCAGCTCGGGACTACCCCCGCAAGCACGGGGACCACTGGGATGAACTGGCCCGCGGCGGCGGAGCGACGGGATCACCCCCGCACGCGCGGGGACCACTACAACGCCCCCGGCGGCCACACGGTGCGCTGGGGACCACCCCCGCACGCGCGGGGACCACGTCCGCGCCGCCCACCGCGGGACGATTGCTCTGGGACCACCCCCGCACGCGCGGGGACCACCGGCACATCGCGCGATCACCAGAGACGAGCACGGGACCACCCCCGCACGCGCGGGGACCACACCGCGCGGTAGGCCTCCTCGATGGCGGCGAGGGGACCACCCCCGCACGCGCGGGGACCACGAGGTGACCACCGCGGTGAACCGTGTCGCCCTGGGACCACCCCCGCACGCGCGGGGACCACGACGGTCTTCGCGGCTTCCCTGCGAAGTCGACGGGACCACCCCCGCACGCGCGGGGACCACCCGCCCGGTCCAGCACCTGGGCCAGCGTCAGGGGGACCACCCCCGCACGCGCGGGGACCACGGCCCGCCGCGGCGGCGGAAACGCGGGGAGGCGGGACCACCCCCGCACGCGCGGGGACCACAATGCGCAACAGGACGAAAGAATGGTGCTGTTGGGACCACCCCCGCACGCGCGGGGACCACGACATCGGCTCGTGGGGCGTCACTGCGGCGGCGGGACCACCCCCGCACGCGCGGGGACCAC

>NZ_CP023690|7|2|5543678-5544438|CRT
CTTGGGGGGCCCGTATGCGCGGGGACCAC	GAGTCGGGTTCGCTGTGCTCGCCGCTCAGCTC
GGGACTACCCCCGCAAGCACGGGGACCAC	TGGGATGAACTGGCCCGCGGCGGCGGAGCGAC
GGGATCACCCCCGCACGCGCGGGGACCAC	TACAACGCCCCCGGCGGCCACACGGTGCGCTG
GGGACCACCCCCGCACGCGCGGGGACCAC	GTCCGCGCCGCCCACCGCGGGACGATTGCTCT
GGGACCACCCCCGCACGCGCGGGGACCAC	CGGCACATCGCGCGATCACCAGAGACGAGCAC
GGGACCACCCCCGCACGCGCGGGGACCAC	ACCGCGCGGTAGGCCTCCTCGATGGCGGCGAG
GGGACCACCCCCGCACGCGCGGGGACCAC	GAGGTGACCACCGCGGTGAACCGTGTCGCCCT
GGGACCACCCCCGCACGCGCGGGGACCAC	GACGGTCTTCGCGGCTTCCCTGCGAAGTCGAC
GGGACCACCCCCGCACGCGCGGGGACCAC	CCGCCCGGTCCAGCACCTGGGCCAGCGTCAGG
GGGACCACCCCCGCACGCGCGGGGACCAC	GGCCCGCCGCGGCGGCGGAAACGCGGGGAGGC
GGGACCACCCCCGCACGCGCGGGGACCAC	AATGCGCAACAGGACGAAAGAATGGTGCTGTT
GGGACCACCCCCGCACGCGCGGGGACCAC	GACATCGGCTCGTGGGGCGTCACTGCGGCGGC
GGGACCACCCCCGCACGCGCGGGGACCAC

>NZ_CP023690|7|7|5543739-5544438|CRISPRCasFinder
GGGACTACCCCCGCAAGCACGGGGACCAC	TGGGATGAACTGGCCCGCGGCGGCGGAGCGAC
GGGATCACCCCCGCACGCGCGGGGACCAC	TACAACGCCCCCGGCGGCCACACGGTGCGCTG
GGGACCACCCCCGCACGCGCGGGGACCAC	GTCCGCGCCGCCCACCGCGGGACGATTGCTCT
GGGACCACCCCCGCACGCGCGGGGACCAC	CGGCACATCGCGCGATCACCAGAGACGAGCAC
GGGACCACCCCCGCACGCGCGGGGACCAC	ACCGCGCGGTAGGCCTCCTCGATGGCGGCGAG
GGGACCACCCCCGCACGCGCGGGGACCAC	GAGGTGACCACCGCGGTGAACCGTGTCGCCCT
GGGACCACCCCCGCACGCGCGGGGACCAC	GACGGTCTTCGCGGCTTCCCTGCGAAGTCGAC
GGGACCACCCCCGCACGCGCGGGGACCAC	CCGCCCGGTCCAGCACCTGGGCCAGCGTCAGG
GGGACCACCCCCGCACGCGCGGGGACCAC	GGCCCGCCGCGGCGGCGGAAACGCGGGGAGGC
GGGACCACCCCCGCACGCGCGGGGACCAC	AATGCGCAACAGGACGAAAGAATGGTGCTGTT
GGGACCACCCCCGCACGCGCGGGGACCAC	GACATCGGCTCGTGGGGCGTCACTGCGGCGGC
GGGACCACCCCCGCACGCGCGGGGACCAC

>NZ_CP023690|7|2|5543861-5544438|PILER-CR
GGGACCACCCCCGCACGCGCGGGGACCAC	GTCCGCGCCGCCCACCGCGGGACGATTGCTCT
GGGACCACCCCCGCACGCGCGGGGACCAC	CGGCACATCGCGCGATCACCAGAGACGAGCAC
GGGACCACCCCCGCACGCGCGGGGACCAC	ACCGCGCGGTAGGCCTCCTCGATGGCGGCGAG
GGGACCACCCCCGCACGCGCGGGGACCAC	GAGGTGACCACCGCGGTGAACCGTGTCGCCCT
GGGACCACCCCCGCACGCGCGGGGACCAC	GACGGTCTTCGCGGCTTCCCTGCGAAGTCGAC
GGGACCACCCCCGCACGCGCGGGGACCAC	CCGCCCGGTCCAGCACCTGGGCCAGCGTCAGG
GGGACCACCCCCGCACGCGCGGGGACCAC	GGCCCGCCGCGGCGGCGGAAACGCGGGGAGGC
GGGACCACCCCCGCACGCGCGGGGACCAC	AATGCGCAACAGGACGAAAGAATGGTGCTGTT
GGGACCACCCCCGCACGCGCGGGGACCAC	GACATCGGCTCGTGGGGCGTCACTGCGGCGGC
GGGACCACCCCCGCACGCGCGGGGACCAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150512458.1\|5556934_5557189_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512445.1\|5536078_5536381_-\|PLDc-N-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|379161
NZ_CP023690.1\|WP_144320328.1\|5540320_5541484_+\|aminofutalosine-synthase-MqnE	unknown	unknown	gnl\|CDD\|213851
NZ_CP023690.1\|WP_150512444.1\|5535040_5535961_-\|isopenicillin-N-synthase-family-oxygenase	unknown	unknown	gnl\|CDD\|226022
NZ_CP023690.1\|WP_150512457.1\|5556264_5556756_-\|cupin-domain-containing-protein	unknown	unknown	gnl\|CDD\|380345
NZ_CP023690.1\|WP_030685386.1\|5534707_5535034_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|197713
NZ_CP023690.1\|WP_150512447.1\|5537917_5538820_+\|4-hydroxybenzoate-octaprenyltransferase	unknown	unknown	gnl\|CDD\|183814
NZ_CP023690.1\|WP_150512456.1\|5554853_5556251_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP023690.1\|WP_150515676.1\|5549013_5549631_+\|TetR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224228
NZ_CP023690.1\|WP_150512454.1\|5552123_5553704_+\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|312032
NZ_CP023690.1\|WP_150512452.1\|5549616_5550465_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366711
NZ_CP023690.1\|WP_030685400.1\|5539811_5540267_+\|Lrp/AsnC-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|214628
NZ_CP023690.1\|WP_150512455.1\|5553717_5554587_-\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|375319
NZ_CP023690.1\|WP_150512451.1\|5548319_5548766_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP023690.1\|WP_150512448.1\|5538816_5539530_+\|UbiX-family-flavin-prenyltransferase	unknown	unknown	gnl\|CDD\|223241
NZ_CP023690.1\|WP_150512449.1\|5541590_5541881_+\|DUF4229-domain-containing-protein	unknown	unknown	gnl\|CDD\|379415
NZ_CP023690.1\|WP_150512450.1\|5544800_5545718_+\|phosphotransferase	unknown	unknown	gnl\|CDD\|366736
NZ_CP023690.1\|WP_150512453.1\|5550527_5551841_-\|3-oxoacyl-ACP-reductase	unknown	unknown	gnl\|CDD\|236207
NZ_CP023690.1\|WP_150512446.1\|5536469_5537921_+\|menaquinone-biosynthesis-decarboxylase	unknown	unknown	gnl\|CDD\|163413
NZ_CP023690.1\|WP_150515675.1\|5542272_5543604_+\|cation:dicarboxylase-symporter-family-transporter	unknown	unknown	gnl\|CDD\|224220

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150512445.1\|5536078_5536381_-\|PLDc-N-terminal-domain-containing-protein	gnl\|CDD\|379161	pfam13396, PLDc_N, Phospholipase_D-nuclease N-terminal. This family is often found at the very N-terminus of proteins from the phospholipase_D-nuclease family, PLDc, pfam00614. However, a large number of members are full-length within this family.	0.000438116
NZ_CP023690.1\|WP_144320328.1\|5540320_5541484_+\|aminofutalosine-synthase-MqnE	gnl\|CDD\|213851	TIGR03700, mena_SCO4494, putative menaquinone biosynthesis radical SAM enzyme, SCO4494 family. Members of this protein family appear to be involved in menaquinone biosynthesis by an alternate pathway via futalosine, based on close phylogenetic correlation with known markers of the futalosine pathway, gene clustering in many organisms, and paralogy with the SCO4550 protein. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP023690.1\|WP_150512444.1\|5535040_5535961_-\|isopenicillin-N-synthase-family-oxygenase	gnl\|CDD\|226022	COG3491, PcbC, Isopenicillin N synthase and related dioxygenases [General function prediction only].	9.87049e-54
NZ_CP023690.1\|WP_150512457.1\|5556264_5556756_-\|cupin-domain-containing-protein	gnl\|CDD\|380345	cd02215, cupin_QDO_N_C, quercetinase, N- and C-terminal cupin domains. This family contains quercetinase (also known as quercetin 2,3-dioxygenase, 2,3QD, QDO and YxaG; EC 1.13.11.24), a mononuclear copper-dependent dioxygenase that catalyzes the cleavage of the flavonol quercetin (5,7,3',4'-tetrahydroxyflavonol) heterocyclic ring to produce 2-protocatechuoyl-phloroglucinol carboxylic acid and carbon monoxide. Bacillus subtilis quercetin 2,3-dioxygenase (QDO) is a homodimer that shows oxygenase activity with several divalent metals such as Mn2+, Co2+, Fe2+, and Cu2+, although the preferred one appears to be Mn2+. The dioxygen binds to the metal ion of the Cu-QDO-quercetin complex, yielding a Cu2+-superoxo quercetin radical intermediate, which then forms a Cu2+-alkylperoxo complex which then evolves into endoperoxide intermediate that decomposes to the product. Quercetinase is a bicupin with two tandem cupin beta-barrel domains, both of which are included in this alignment model. The pirins, which also belong to the cupin domain family, have been shown to catalyze a reaction involving quercetin and may have a function similar to that of quercetinase.	5.78665e-16
NZ_CP023690.1\|WP_030685386.1\|5534707_5535034_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|197713	smart00418, HTH_ARSR, helix_turn_helix, Arsenical Resistance Operon Repressor.	1.45825e-07
NZ_CP023690.1\|WP_150512447.1\|5537917_5538820_+\|4-hydroxybenzoate-octaprenyltransferase	gnl\|CDD\|183814	PRK12888, ubiA, 4-hydroxybenzoate octaprenyltransferase.	1.68465e-172
NZ_CP023690.1\|WP_150512456.1\|5554853_5556251_+\|MFS-transporter	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	6.96803e-58
NZ_CP023690.1\|WP_150515676.1\|5549013_5549631_+\|TetR-family-transcriptional-regulator	gnl\|CDD\|224228	COG1309, AcrR, Transcriptional regulator [Transcription].	1.7487e-14
NZ_CP023690.1\|WP_150512454.1\|5552123_5553704_+\|alpha/beta-fold-hydrolase	gnl\|CDD\|312032	pfam08386, Abhydrolase_4, TAP-like protein. This is a family of putative bacterial peptidases and hydrolases that bear similarity to a tripeptidyl aminopeptidase isolated from Streptomyces lividans. A member of this family is thought to be involved in the C-terminal processing of propionicin F, a bacteriocidin characterized from Propionibacterium freudenreichii.	7.15779e-25
NZ_CP023690.1\|WP_150512452.1\|5549616_5550465_-\|hypothetical-protein	gnl\|CDD\|366711	pfam01575, MaoC_dehydratas, MaoC like domain. The maoC gene is part of a operon with maoA which is involved in the synthesis of monoamine oxidase. The MaoC protein is found to share similarity with a wide variety of enzymes; estradiol 17 beta-dehydrogenase 4, peroxisomal hydratase-dehydrogenase-epimerase, fatty acid synthase beta subunit. Several bacterial proteins that are composed solely of this domain have (R)-specific enoyl-CoA hydratase activity. This domain is also present in the NodN nodulation protein N.	1.04851e-13
NZ_CP023690.1\|WP_030685400.1\|5539811_5540267_+\|Lrp/AsnC-family-transcriptional-regulator	gnl\|CDD\|214628	smart00344, HTH_ASNC, helix_turn_helix ASNC type. AsnC: an autogenously regulated activator of asparagine synthetase A transcription in Escherichia coli).	2.20402e-35
NZ_CP023690.1\|WP_150512455.1\|5553717_5554587_-\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|375319	pfam17765, MLTR_LBD, MmyB-like transcription regulator ligand binding domain. This domain is found in a family of actinobacterial transcription factors. The structure shows it has a PAS domain like fold and it is bound to Myristic acid.	6.42908e-57
NZ_CP023690.1\|WP_150512451.1\|5548319_5548766_+\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	1.508e-08
NZ_CP023690.1\|WP_150512448.1\|5538816_5539530_+\|UbiX-family-flavin-prenyltransferase	gnl\|CDD\|223241	COG0163, UbiX family flavin prenyltransferase [Coenzyme transport and metabolism].	4.3712e-65
NZ_CP023690.1\|WP_150512449.1\|5541590_5541881_+\|DUF4229-domain-containing-protein	gnl\|CDD\|379415	pfam14012, DUF4229, Protein of unknown function (DUF4229). This family of integral membrane proteins is functionally uncharacterized. This family of proteins is found in bacteria. Proteins in this family are typically between 95 and 122 amino acids in length.	7.86191e-16
NZ_CP023690.1\|WP_150512450.1\|5544800_5545718_+\|phosphotransferase	gnl\|CDD\|366736	pfam01636, APH, Phosphotransferase enzyme family. This family consists of bacterial antibiotic resistance proteins, which confer resistance to various aminoglycosides they include: aminoglycoside 3'-phosphotransferase or kanamycin kinase / neomycin-kanamycin phosphotransferase and streptomycin 3''-kinase or streptomycin 3''-phosphotransferase. The aminoglycoside phosphotransferases inactivate aminoglycoside antibiotics via phosphorylation. This family also includes homoserine kinase. This family is related to fructosamine kinase pfam03881.	2.08138e-17
NZ_CP023690.1\|WP_150512453.1\|5550527_5551841_-\|3-oxoacyl-ACP-reductase	gnl\|CDD\|236207	PRK08261, fabG, 3-ketoacyl-(acyl-carrier-protein) reductase; Provisional.	0
NZ_CP023690.1\|WP_150512446.1\|5536469_5537921_+\|menaquinone-biosynthesis-decarboxylase	gnl\|CDD\|163413	TIGR03701, mena_SCO4490, menaquinone biosynthesis decarboxylase, SCO4490 family. Members of this protein family are putative decarboxylases involved in a late stage of the alternative pathway for menaquinone, via futalosine, as in Streptomyces coelicolor and Helicobacter pylori. [Biosynthesis of cofactors, prosthetic groups, and carriers, Menaquinone and ubiquinone].	0
NZ_CP023690.1\|WP_150515675.1\|5542272_5543604_+\|cation:dicarboxylase-symporter-family-transporter	gnl\|CDD\|224220	COG1301, GltP, Na+/H+-dicarboxylate symporters [Energy production and conversion].	6.99917e-112

>NZ_CP023690.1|WP_150515675.1|5542272_5543604_+|cation:dicarboxylase-symporter-family-transporter
MSANSATPAGEPKPGFRIPKFLKLPFWAQILGGLVLGVLLGWLARSQDISWLVTTLSKVGDTFIGLLKLAVAPLVFFAILISITNLRKVNNAARLATRTLLWFMITSLIAVVIGLVIGLVTNPGAGTGLTPKDGAKPEHEGSWIDFLTGIIPTDVITPFTELNVLQIVFMAAVAGVAILKIGDEKAKPILDLSESILTLLQKALWWVIKLSPIGTIGLIGFAIADYGWNLISKYATFTADIYIGCALVMFGVYPLLLATVAKVSPLQFFKGAWPAIQLAFVSRSSVGTMPLTQKVTERLGVPKEYTSFAVPFGATTKMDGCAAIYPAIAAIFVAQIFDVNMGIKEYLLIAFVSVVGSAATAGLTGATVMLTLTLSTLGLPMEGVGLLLAIDPVLDMMRTATNVAGQALVPVLVAARENILDREAYEHASASPIDEPDVVPANA
>NZ_CP023690.1|WP_150512449.1|5541590_5541881_+|DUF4229-domain-containing-protein
MLRYTLMRLGVFAGCFLVVWGLVYSGIVPRGLGGSNLLWVALLSLVVSAPLSFVLLRKERDRASEKVVAKVDNVKASLERNRTQEDGADDATRTAQ
>NZ_CP023690.1|WP_144320328.1|5540320_5541484_+|aminofutalosine-synthase-MqnE
MDAGLKRDLEEKVRSGERLSREDGIALYESDDLAWLGGLAHEVRTRKNGDVVHFNVNRHLNMTNVCTASCAYCSFQRKPGEKDAYTMRIEEAVRLAKAMEADNLTELHIVNGLHPNLPWRYYPRSLRELKAALPNVSLKAFTATEIHHFETISGLSASEILDELIDAGLESLTGGGAEIFDWEVRQHIVDHKTHWEDWSRIHRLAHEKGLKTPATMLYGHIEEPRHRVDHVLRLRELQDETGGFQVFIPLRYQHDFVDMQDGKVRNRLQARTKMASGIEALKTFAVSRLLFDNVPHVKVFWVMHGLATAQLALQHGADDMDGSVVEYKITHDADNFGTPNKLTRDDLLDLIREAGFRPVERNTRYEVIREFPGPDRELRESPQPMRL
>NZ_CP023690.1|WP_030685400.1|5539811_5540267_+|Lrp/AsnC-family-transcriptional-regulator
MDAVDRQLIQALRENGRASYAELGRLVGLSGPSVTDRINRLEAAGVITGYRATVDSASLGLGVTALIGISLSDAADHEDVARRLRDLHEIEDCWFIAGDDSYMLKVRASDVDGLEKTIRRLSGTKGVSRTRTTIVLSTKWENRVGELPEEV
>NZ_CP023690.1|WP_150512448.1|5538816_5539530_+|UbiX-family-flavin-prenyltransferase
MTGRTEPVDRLRGVNAGDTERRPWVVGVSGASGTPYAAAVLRALLAAGESVDLVVSRASRLTLLDETGISFRDAHWRADLEQWLARGADGKPDTFRVRTDDVRYWAAGDLAAGPSSGSYATKGMLIVPASTACVAGVALGLSKDLLQRVASVTLKEGRRLVVCVRETPLNGQTLRHLVSLDEAGAIVLPASPAFYAGATHIQDLVDFVAGRMLDAAQVPHRLYRRWEGELGGGSREG
>NZ_CP023690.1|WP_150512447.1|5537917_5538820_+|4-hydroxybenzoate-octaprenyltransferase
MSSASAALPQPGRTKAFLRLVMIEHSVFALPFAYIASLTAMYEWDKNIHWGRLLLVTICMVGLRTFAMAANRIIDREIDARNPRTAHRELVTGAVTVKSAWTGALVAVVVFLGSAALLNPLCLALAPVAVIPMVVYPYGKRFTNFPQAILGIAQAMGPIGAWLAITGEWSWTAVILGLAVGVWIGGFDLIYACQDVESDREAGVLSVPARFGVPASIRGARGCHAVTTALLVWYAVQTGAGAFFWLGLLIVAGAFLYEHSIVRPHDLSRLNRAFFQVNGFIGIALFVCALLDLLVRGLTV
>NZ_CP023690.1|WP_150512446.1|5536469_5537921_+|menaquinone-biosynthesis-decarboxylase
MAYDDLRSLLRALEREGDLKRIKAEVDPYLEVGEIVDRVQKSGGPALLFENVKGSDMPLAMNVFGTDRRLLKALGLKSYGEISEKIGGLLRPELPQGFVGVREAFGKLGAMTHVPPKKVKDAPVQEVVLRGEDVDLDRLPALFTWPKDGGSFFNLGLTHTKDPESGVRNLGLYRLQRHDRRTIGMHWQIHKDSRNHYQVAARRGERLPVAIAFGCPPAVTYASTAPLPGDIDEYLFAGFLQGKRIEMVDCKTVPLQVPAQAEVVLEGWLEPGEMLPEGPFGDHTGFYTPQEPFPALTIDCVTMRKRPLLQSIVVGRPPTEDGPLGRATERFFLPLLKIIVPDIVDYHLPESGGFHNCAIVSIDKKYPKHAQKVMHAIWGAHMMSLTKLIVVVDSDCDVHDLHEVSWRALGNTDYARDLTVVEGPVDHLDHASYQQFWGGKAGIDATKKWPEEGYTRDGGWPDMVESDPDTAALVDRRWREYGL
>NZ_CP023690.1|WP_150512445.1|5536078_5536381_-|PLDc-N-terminal-domain-containing-protein
MLRYLPFLLVLAVWIYAFIDVLNTPEKEVRHLPKVVWVIIVLLFGEVLLGPIAWFVTGKKRGPATGRAGGSRGGWVAPDDNPEFLKNLNKDLDDKRDEGK
>NZ_CP023690.1|WP_150512444.1|5535040_5535961_-|isopenicillin-N-synthase-family-oxygenase
MTIPTVDLRAWRSGPPEARQEIKRAVDDGLRTAGFLLVTGHDVAPGLRTAIREESRSFFRLPPEAKQPYSVRVGARGWLGPGAEANSYAEGTPSPPDLKESLSFAADEPTGDAAVDAEWFAPNTWPAETPGLRACVETYLRLMRTLSDQLLELLAAALGEPEDFFTRHTGHPTWGFNINWYPGRDRVGTPEPGQFRIGPHTDFGTVTVLDRQAGRGGLQVFTDADGWQDAPWDPEAFTINIGDLMARWTGGRWRSGRHRVLPPPADVPAEELMSLVYFYECDPGTDVRGIDSHVYLRAQLDAIASG
>NZ_CP023690.1|WP_030685386.1|5534707_5535034_+|helix-turn-helix-domain-containing-protein
MAPRTSHRAAPVHARLDDVTVQEALAALADPVRLRLVRELAGSADWSRACGSFDVPVGKAALSHHFAALRAAGLVEQRDEGPRRVNRLRREEFDARFPGLLALVLRGD
>NZ_CP023690.1|WP_150512450.1|5544800_5545718_+|phosphotransferase
MAADAGQGSEKGFMEAGATRVMTAACRAAGLDDRDAELIRLGENALFRLASAPVIVRVARGPEWLTKARNEVAVSRWLTGEGFPATRAVEDLEQPLVIDGHPVTFWHLIVEADRKATYGELGGVLRDLHSMTVPEGLHLPSYEPFDKSDVRLDKAVIPDDDKAFLRKRARELRDKCAELRFETPKGPVHGDAHVQNLMVDVQGRVILIDFEVFCFDHPEWDLMVTSVEHHSLGWQTEQQYADFVGAYGRDLYDWEGYATLRGLQEFNMTTWLMQNVRVSERVADEYRRRIAALRDDDGPRDWRPW
>NZ_CP023690.1|WP_150512451.1|5548319_5548766_+|ATP-binding-protein
MGARPSKNRANTSGMAAPRADAADSSAGHHRALTLSADSRDAVRAAREMVRGSLQDWGLERIGDDARLAVSELVSNVVQHAVPDNCLAQPGARRRIDISVMTWPGLLCIGVTDEDSAPPDLPVGDRLSPELAGDFPEALLPERGRGLS
>NZ_CP023690.1|WP_150515676.1|5549013_5549631_+|TetR-family-transcriptional-regulator
MPRAVRERQMLDAAVRTFGQRGYRAASMDEIAELAGVSKPLVYLYLNSKEDLFTACIRREAAALTQAVRSAVNPDAPADQQLWDGLRAFFEHTALHPDAWAVLHSQARTVGEPFAAEVNAARAEIVAFVTALIGAAARAAHRDPSLPDREVAGLAHALVGAAESLAGWANTEPSVPAKEAAATLMNFAWAGLGDLMEGRPWSPPA
>NZ_CP023690.1|WP_150512452.1|5549616_5550465_-|hypothetical-protein
MPRPPLPLTLLKGAFLSPLKHPGTGHGNGGPRLRDRARATPGRADAYRRVCGFAPTGEPPGDTLPLPYPHVLAFPLTTRLMAARAFPLPLLGLVHTSIEVVRHRALRPTDDLGLTAYVEKLAPHRRGTEATLTVEATVDGTIAWESRSTYLARHETGATAPPRQGPGDEPPLPVEARWRLAAGLGRRYAAVSGDRNPIHLHPLTARPFGFPRPIAHGMWTFARCLAEYGPTGTEPVRVTARFRAPVLLPATVTYGRRGQHFELRDSTGRPHVRGRVEPLGGR
>NZ_CP023690.1|WP_150512453.1|5550527_5551841_-|3-oxoacyl-ACP-reductase
MADRYLTFTRTAPGRFLTRRLGLPRPVPLRRFSPEHPALDGPLLHLTAGDLPLPGLHEVLTRTGLPPHTGPLGTRHPAAVVLDATGVATVSALVDVHATLHPVVRSIADCGRVVVLGAPLSPADHHQAAAQQALDGFVRSLAKELGRGRTATLVRTASAPATEPTLRFLLSPKSAYVNGQTIEVTPDAHAPENDSPGRPLAGRTALVTGAARGIGAAVAEVLARDGARVVALDVPAARTDLVRVAERVGGAPLALDITADDAGERIAAALPGGLDVLVHNAGITRDRRLANMAADRWSSVLDVNLGSVLRTTDFLLKSGTLRRGGSVVATASVAGLAGNAGQTNYAASKAGVAGLVRSLAPRALAEHGITVNAVAPGFIETRMTAAVPLLIREAGRRLNSLAQGGQPVDVAETVAWLALGGVNAQVIRVCGQSLLGA
>NZ_CP023690.1|WP_150512454.1|5552123_5553704_+|alpha/beta-fold-hydrolase
MEAAVRTPALTGVTALALALTALPAATGAEPPRPDLKRFYAQKVKWAVCTPEKQNLPETVTKNEDVRCGTLTVPLDYARPRSGTVDLALLKVKASGKKRGSLLVNFGGPGGPGVAGLAADLKGFGDLGKGYDVVGFDPRGVGLSEPVSCGDEPEPEGLDDPDDAGAVLEQLRRTAERCVKESGPVLPHIGTVNVSRDMDVMRAALGDKKLNYLGFSYGTRLGAVYAAQFPKKVGRMVLDGVDTLTEPVDEQGLASAEGQQTALDNFLLWCTKNAGCVFGDDSRRARETMVKVIEDLDAMPLRSTDGAEFTGQDVVSVLGSALYSRQAWPALSQALGALLADGDPRALMRVGGAGGMGVGHGFGRGFGHGFGHGRQDVPQDNETAALAAVNCADDPDRPGARKVEKEIGRLQQEFEEVSPVFGEHNLTLVLMCFGWPAGTSYIRKEVRDVDTPKLLLVGTRGDPATPYRWTEETARRLGSSAVVLDNKGDGHTGYFGSKCVKAKVDGFLLYKQLPANGSSCAAEWRE
>NZ_CP023690.1|WP_150512455.1|5553717_5554587_-|helix-turn-helix-domain-containing-protein
MKSNGGTELGRYLRARRAQIRPEDTGLPAGTGIRRTPGLRREELATLAGVSVDYYTRLERGRESNPSPAVVDALARALHLRGDAHERLHELAELASGRLTEPRPTAEFTVRESVHRMLEALRPLPAYVVGPYSDMLAANAPCRRLMPGLWDWPAQERNLVRYLFLHPVGRTLYVPWEETVALSIAHLRAVGGRDPDSPRLTALVGELMLKSPDFARLWDRYEVCERGGGVKSFAHPKVGPMTLTYEVMSLARTGGQRLVTYQAEPGSADEAAMLRLDSASRTAAEPSTR
>NZ_CP023690.1|WP_150512456.1|5554853_5556251_+|MFS-transporter
MPLTLQAPAPPRPTPRAATALLASLLGFTVITVDVSAVNIALPDIRSSLHGGMTGLQWVVDAYTLMFAALMISAGALADRAGARRAYAWGTALFTLASLACALAPGIGALIAARVGQGAAAAVVMPASLALIRQAYDDPRQRARAIALWTVGGSAAMAAGPVLGGVLTQTVGWRAVFLLNLPIGALILALLTRTAPSPRRPAPLDVPGQLTAVLGLGALAYAVIEGGHAGPTSPSVLVAAGLAVAAVFAFRAAERRHPAPMVPLPLLRQREVGVSLAVGFAVNAGFYGVVFLLGLYLQQLRGMSAVAAGLTFVPLAVLITSTNLVSPRFAERAGRRPVIVTGQLILAVAMFALLPLAADTPMWLVLVLLVPTGIGGALAVPALTALLMDAVPGHRAGTASGLLNSLRQTGGALSVALFGALIGSGGGYSVGGMRQGLVVVGLVLLGTAALSVWRLPRGVPRGGGR
>NZ_CP023690.1|WP_150512457.1|5556264_5556756_-|cupin-domain-containing-protein
MSYPDPRYFSDKGEVSAVFRPADTPPDHSTPTQDYHYLATTVVTQGEFGLYKVDMGPRAGGPTTHFHKGISESFYVLDGELELYDGDRWRTGGPGDFLYVPVGGLHAFRNASDAPTSMLMLFAPGAPREEYFENVAEMARRGGDEFGRFLVEHDSFFVDQGYR
>NZ_CP023690.1|WP_150512458.1|5556934_5557189_-|hypothetical-protein
MAGSDTDGIALELERLHRSVDVGFATTRGDLALLLQRADQTDKALSEHEERLDALERTRWPLPSLAAVTSCTALALTLWQQSGR

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Crispr_ID: NZ_CP023690_9

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_9

5844414-5844579

Orphan

Consensus_repeat	Method
CGGTGCGGGGTTGGTCCCACCCTCCGCCCCCACCCGGCTCTGCGTCGGGCCCGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_9

>merge|NZ_CP023690|9|5844414-5844579|CRISPRCasFinder
CGGTGCGGGGTTGGTCCCACCCTCCGCCCCCACCCGGCTCTGCGTCGGGCCCGGGCCTGCGGGGCGGTTGCTCGGCGCTTGGGCTGTGCCCGTAGCCCTGGGGTGGCTTTGCCGGTGCGGGGTTGGTCCCACCCTCCGCCCCCACCCGGCTCTGCGTCGCGCCCGG

>NZ_CP023690|9|9|5844414-5844579|CRISPRCasFinder
CGGTGCGGGGTTGGTCCCACCCTCCGCCCCCACCCGGCTCTGCGTCGGGCCCGG	GCCTGCGGGGCGGTTGCTCGGCGCTTGGGCTGTGCCCGTAGCCCTGGGGTGGCTTTGC
CGGTGCGGGGTTGGTCCCACCCTCCGCCCCCACCCGGCTCTGCGTCGCGCCCGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150512649.1\|5834514_5835150_-\|RDD-family-protein	unknown	unknown	gnl\|CDD\|377640
NZ_CP023690.1\|WP_150512658.1\|5845124_5846114_+\|malate-dehydrogenase	unknown	unknown	gnl\|CDD\|235468
NZ_CP023690.1\|WP_150512651.1\|5836272_5836755_+\|DUF3017-domain-containing-protein	unknown	unknown	gnl\|CDD\|378602
NZ_CP023690.1\|WP_170316491.1\|5839126_5839477_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|366589
NZ_CP023690.1\|WP_150512657.1\|5842727_5844005_+\|DUF2690-domain-containing-protein	unknown	unknown	gnl\|CDD\|371292
NZ_CP023690.1\|WP_150512663.1\|5850890_5851865_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176149
NZ_CP023690.1\|WP_150512656.1\|5840557_5841493_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|379262
NZ_CP023690.1\|WP_150512650.1\|5835398_5836256_+\|bifunctional-methylenetetrahydrofolate-dehydrogenase/methenyltetrahydrofolate-cyclohydrolase	unknown	unknown	gnl\|CDD\|237637
NZ_CP023690.1\|WP_150512655.1\|5839772_5840561_+\|peptidoglycan-binding-protein	unknown	unknown	gnl\|CDD\|366659
NZ_CP023690.1\|WP_150512653.1\|5838345_5839038_+\|response-regulator	unknown	unknown	gnl\|CDD\|225107
NZ_CP023690.1\|WP_150512659.1\|5846303_5848187_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512665.1\|5852368_5852875_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370676
NZ_CP023690.1\|WP_150512662.1\|5849388_5850792_-\|MFS-transporter	unknown	unknown	gnl\|CDD\|129794
NZ_CP023690.1\|WP_150512661.1\|5848582_5849368_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512648.1\|5832848_5834444_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	unknown	unknown	gnl\|CDD\|234854
NZ_CP023690.1\|WP_150512666.1\|5853473_5854013_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_030668867.1\|5853224_5853470_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224393
NZ_CP023690.1\|WP_150512660.1\|5848183_5848579_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512664.1\|5851938_5852310_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512652.1\|5837188_5838349_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|226951

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150512649.1\|5834514_5835150_-\|RDD-family-protein	gnl\|CDD\|377640	pfam06271, RDD, RDD family. This family of proteins contain three highly conserved amino acids: one arginine and two aspartates, hence the name of RDD family. This region contains two predicted transmembrane regions. The arginine occurs at the N-terminus of the first helix and the first aspartate occurs in the middle of this helix. The molecular function of this region is unknown. However this region may be involved in transport of an as yet unknown set of ligands (Bateman A pers. obs.).	5.58131e-24
NZ_CP023690.1\|WP_150512658.1\|5845124_5846114_+\|malate-dehydrogenase	gnl\|CDD\|235468	PRK05442, PRK05442, malate dehydrogenase; Provisional.	0
NZ_CP023690.1\|WP_150512651.1\|5836272_5836755_+\|DUF3017-domain-containing-protein	gnl\|CDD\|378602	pfam11222, DUF3017, Protein of unknown function (DUF3017). This bacterial family of proteins with unknown function appear to be restricted to Actinobacteria.	4.50542e-19
NZ_CP023690.1\|WP_170316491.1\|5839126_5839477_-\|hypothetical-protein	gnl\|CDD\|366589	pfam01356, A_amylase_inhib, Alpha amylase inhibitor.	0.0047963
NZ_CP023690.1\|WP_150512657.1\|5842727_5844005_+\|DUF2690-domain-containing-protein	gnl\|CDD\|371292	pfam10901, DUF2690, Protein of unknown function (DUF2690). This bacterial family of proteins has no known function.	1.78257e-15
NZ_CP023690.1\|WP_150512663.1\|5850890_5851865_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|176149	cd08460, PBP2_DntR_like_1, The C-terminal substrate binding domain of an uncharacterized LysR-type transcriptional regulator similar to DntR, which is involved in the catabolism of dinitrotoluene; contains the type 2 periplasmic binding fold. This CD includes an uncharacterized LysR-type transcriptional regulator similar to DntR, NahR, and LinR, which are involved in the degradation of aromatic compounds. The transcription of the genes encoding enzymes involved in such degradation is regulated and expression of these enzymes is enhanced by inducers, which are either an intermediate in the metabolic pathway or compounds to be degraded. This substrate-binding domain shows significant homology to the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	9.17705e-78
NZ_CP023690.1\|WP_150512656.1\|5840557_5841493_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|379262	pfam13560, HTH_31, Helix-turn-helix domain. This domain is a helix-turn-helix domain that probably binds to DNA.	2.19331e-07
NZ_CP023690.1\|WP_150512650.1\|5835398_5836256_+\|bifunctional-methylenetetrahydrofolate-dehydrogenase/methenyltetrahydrofolate-cyclohydrolase	gnl\|CDD\|237637	PRK14193, PRK14193, bifunctional 5,10-methylene-tetrahydrofolate dehydrogenase/ 5,10-methylene-tetrahydrofolate cyclohydrolase; Provisional.	0
NZ_CP023690.1\|WP_150512655.1\|5839772_5840561_+\|peptidoglycan-binding-protein	gnl\|CDD\|366659	pfam01471, PG_binding_1, Putative peptidoglycan binding domain. This domain is composed of three alpha helices. This domain is found at the N or C-terminus of a variety of enzymes involved in bacterial cell wall degradation. This domain may have a general peptidoglycan binding function. This family is found N-terminal to the catalytic domain of matrixins. The domain is found to bind peptidoglycan experimentally.	5.97468e-18
NZ_CP023690.1\|WP_150512653.1\|5838345_5839038_+\|response-regulator	gnl\|CDD\|225107	COG2197, CitB, Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain [Signal transduction mechanisms / Transcription].	4.32339e-79
NZ_CP023690.1\|WP_150512665.1\|5852368_5852875_-\|hypothetical-protein	gnl\|CDD\|370676	pfam09770, PAT1, Topoisomerase II-associated protein PAT1. Members of this family are necessary for accurate chromosome transmission during cell division.	0.00415181
NZ_CP023690.1\|WP_150512662.1\|5849388_5850792_-\|MFS-transporter	gnl\|CDD\|129794	TIGR00711, Uncharacterized_MFS-type_transporter_YhcA, drug resistance transporter, EmrB/QacA subfamily. This subfamily of drug efflux proteins, a part of the major faciliator family, is predicted to have 14 potential membrane-spanning regions. Members with known activities include EmrB (multiple drug resistance efflux pump) in E. coli, FarB (antibacterial fatty acid resistance) in Neisseria gonorrhoeae, TcmA (tetracenomycin C resistance) in Streptomyces glaucescens, etc. In most cases, the efflux pump is described as having a second component encoded in the same operon, such as EmrA of E. coli. [Cellular processes, Toxin production and resistance, Transport and binding proteins, Other].	1.3729e-48
NZ_CP023690.1\|WP_150512648.1\|5832848_5834444_+\|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase	gnl\|CDD\|234854	PRK00881, purH, bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase; Provisional.	0
NZ_CP023690.1\|WP_030668867.1\|5853224_5853470_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|224393	COG1476, COG1476, Predicted transcriptional regulators [Transcription].	8.20812e-22
NZ_CP023690.1\|WP_150512652.1\|5837188_5838349_+\|sensor-histidine-kinase	gnl\|CDD\|226951	COG4585, COG4585, Signal transduction histidine kinase [Signal transduction mechanisms].	1.91314e-44

>NZ_CP023690.1|WP_150512657.1|5842727_5844005_+|DUF2690-domain-containing-protein
MPRWKALPDDLDPQVREFASQLRRLVDSSGLSIAAVADRTGYSKTSWERYLNGRLLAPKGAIVALAEVTGTPAVHLVTMWELAERAWSRSEMRHDMTMQAIRISQARAALGEAAAPSPPKGKGGSGKARGGVGAVTGVAGPAGVSPTVPPRHESARYGARTAAQPGAAGGPGPGAAPSSTPAGPSASSAPSAPSSFPAPSSSASSPSSAPSSYEASAAPPTAAASAHASAATAYGGGARGVPAAPVGPDGKSPDGQRRKRKLTMFLAGVVGALVVIGAAAFLTGVGRGDKDDDKAKPSATPTTSTADLPAGVECNGAACAGKDPENMGCGGEFARTTARVTVGTKTLVEVRYSKTCGAAWARITQAKSGDKVQIRGSDGGAAGRQSGTVGGAADVDAYTPMVAVKSGTQAKACATLASGLKACTK
>NZ_CP023690.1|WP_150512656.1|5840557_5841493_+|helix-turn-helix-domain-containing-protein
MKGRAGRDGRGGPSPAPPAAGLPLVEALRELRERTGLSLEALGRRTAYSKSSWERYLNGKKPVPRKAVAALCALADEPPGRLLALWDLADAAWSGRSARGDDASAADRPGGDGAGGDGAGGDGAADDIGTLVGSTGPVPGGAGAARRRRSALALGIAAVVVVAGGVTAGLAVTRDDDRRRDRVATEPGPGPYEPRCVGAACEGRQPQKMGCGGPGQVASLATRSFAPERRVELRVGKACNAVWARATGLLPGDRAVVSLPGARAKELRADEPEDTRRYLATPMTALKGADPADATVCVTFAETATKTCFSG
>NZ_CP023690.1|WP_150512655.1|5839772_5840561_+|peptidoglycan-binding-protein
MPRWKELPAQLGEQERQLLVQLRRMKDHSGLSLASLGAKTSYSGSSWERYLNGKKPVPRAAVEELAQVCGADPTRLLVLHEVARAADGHAEPVDSEAEAVAPEAAAQPVTRASAPPGPPAEAPPAARTVRLRSALTALVLAVAAAFAGGLLAGRALSGDGGDEGRGVFAYAQERTYSCENGRADGVRHAGYSTTATAILDRGSTGWEVVEAQCLLKAHGFGAGKIDGSYGDGTKAAVKRFQRARGLVTDGIVGPDTWGALRK
>NZ_CP023690.1|WP_170316491.1|5839126_5839477_-|hypothetical-protein
MTSSTRMPCDTTDTGWGRKARGHVRATAVGLTAAAVLGGGLTLAPAASAAPQGTAPACVERSVSGRSATATNNCGRVLRVKIVVKHGPDSRCTSLKHRAWARHSWPFGSYDKTVTC
>NZ_CP023690.1|WP_150512653.1|5838345_5839038_+|response-regulator
MTPHIKVLVVDDQFLIRAGLVGVLRAAPGIEVVGEAGDGAEAVELAAEARPDVILMDIRMPGMNGITATERILAAAPDPAPRVLVLTTFDLDEYVYGALRAGAAGFLLKDSGPERLLAAVAAVGSGDALFAPSVTRRLVEAFAQRSGSTPLAGSESPPGLESLTGRELEVLKLIARGLSNAEIADRLYISEATVKTHLNRTMNKLDIDTRAQAVVMAYESGLVTPGDQGL
>NZ_CP023690.1|WP_150512652.1|5837188_5838349_+|sensor-histidine-kinase
MRLRPFTTDLLLALGQVAALVLIGPSANGIGWTPLDTQGYGLGLLVILPTLARSKAPITVCLVTYSVWVVYILAGYWPVVTSFGPLLCLYTVSLLRPTRVSAVLAVLLAALWAFGSLLTLDDSFIPSVVAQCVCFNAMVWRMGYLARRSQELARRTRAEQQEKARRAVVEERGRIARELHDVVAHHMSVISVQAGLAKFVFDSDAKTARAALGTISGTSAEALEEMRRMLRVLRAQEDGGEVPDAPMPGLARIGEMTDRVRAGGVPVEFRVVGTPRPIASGVELCAYRVVQEALTNVLKHARQASATVELHYHHDHIEVSVTDDGEGVIQDRVERGRGHGLIGMRERAKLYGGTISIGPRSSGGFAVRLTLPTSARAAPPGDDVTE
>NZ_CP023690.1|WP_150512651.1|5836272_5836755_+|DUF3017-domain-containing-protein
MSADAKDGTERSEQPTAKGAVSAPGPDGVPRKTSRRFPLFTRDTARPEGGGRAAPGDAPAPARQWPLLVVVSVVALGLLLTAFDVFRVGTILVGLGLLAGAVMRWTLPGVGMLAVRSRFTDMVTYGILGLAIVLLAMMAQPNPWLVIPFLDDTLHFTISS
>NZ_CP023690.1|WP_150512650.1|5835398_5836256_+|bifunctional-methylenetetrahydrofolate-dehydrogenase/methenyltetrahydrofolate-cyclohydrolase
MTAQILDGKATAAAIKSELAVRVAALKEKGVTPGLGTVLVGDDPGSQKYVAGKHRDCAQVGIASIQRELPATASQEEIEAVVRELNEDPACTGYIVQLPLPKGIDENRVLELMDPAKDADGLHPTNLGRLVLNEPAPLPCTPYGIIRLLRQHDVEIKGAEVVVVGRGVTIGRPMPLLLTRKSENATVTQCHTGTRDLASHLRRADIIVAAAGVPHLVKPEDVKPGAAVLDVGVSRDESGKIVGDVHPGVAEVAGWLSPNPGGVGPMTRAQLLVNVVEAAERGAAA
>NZ_CP023690.1|WP_150512649.1|5834514_5835150_-|RDD-family-protein
MSTPPPNPYGQPQQPQPGYGPGYGYPQQAPQGVPPQQGGYPGQNYAPYPQAQPGQSPYGAYPQAAGYGMGHDGRPELAHWGLRVGATLLDGLITIVPLYLVVGLAVGIGGEDMSAGASLVSVLALAYTVFMGFYQIHLEGKTGQSIGKRIVGIRVLREADGRFLGFGMAFVRKLAHFLDSIPCYIGYLWPLWDDKKQCFADKVCGTVVIKG
>NZ_CP023690.1|WP_150512648.1|5832848_5834444_+|bifunctional-phosphoribosylaminoimidazolecarboxamide-formyltransferase/IMP-cyclohydrolase
MTAEGTTPQTPRSSPGADQRPIRRALISVYDKTGLEGLARGLHEAGVELVSTGSTAARIAAAGVPVTKVEELTGFPECLDGRVKTLHPRVHAGILADLRLEAHRKQLQELGVEPFGLVVVNLYPFRETVASGASVDECVEQIDIGGPSMVRAAAKNHPSVAVVTSPSRYGDLLAAVRAGGFDFAARRALAAEAFQHTAAYDVAVANWFLETEEGAGERFPAFVGAAFDLKNQLRYGENPHQSAALYTDGRGGLAEAEQLHGKEMSYNNYTDTDAARRAAYDHDDPCVAIIKHANPCGIAIGGNVAEAHRKAHACDPLSAFGGVIAVNRPVTKEMAEQVAEIFTEVIVAPDYEDGALEALTKKKNIRVLRAPQAPSAPVEVKPIDGGALLQVTDRLQADGDNPASWTLATGDALSPGELAELAFAWRACRAVKSNAILLAKDGASVGVGMGQVNRVDSAKLAVERAGEERARGAYAASDAFFPFPDGLEVLTAAGVKAVVQPGGSVRDELVVEAAKKAGVTMYFTGTRHFFH
>NZ_CP023690.1|WP_150512658.1|5845124_5846114_+|malate-dehydrogenase
MTRTPVNVTVTGAAGQIGYALLFRIASGHLLGADVPVNLRLLEITPALKAAEGTAMELDDCAFPLLNSIEISDDPNVAFDGANVALLVGARPRTKGMERGDLLEANGGIFKPQGKAINDHAADDIKVLVVGNPANTNALIAQAAAPDVPAERFTAMTRLDHNRAISQLAKKTGAAVSDIKRLTIWGNHSATQYPDIFHAEIAGKNAAEVVNDQAWLGDTFIPTVAKRGAAIIEARGASSAASAANAAIDHVHTWVNGTAAGDWTSMGIPSDGSYGVPEGIISSFPVTTKDGKYEIVQGLEINEFSRARIDASVKELSEEREAVRALGLI
>NZ_CP023690.1|WP_150512659.1|5846303_5848187_+|hypothetical-protein
MRGDPPREYQHTESTRLLSVGARQNADFRRRVIGELVGHAERPVAPPLGADVLPVLAHALRARREEIVSALLLFAVWAGFVAADTVMAWDAANDRAGGDAGLSLGDTLLLAFDGDAAEGPGDASGALLPGGWALWFAAVVFLLWCGRIVSGRDTGAGQPLRPLRLPAVLVWLRRRFGWLVTVLAWVFGSTYWFAALTGIAETPYPVIFPLLVTVVVWRHQFRAKRVLRTQLARQVFAETDQPELPARYAGIAECVRREQRAPLTLYDVNRPFVGAGKPRKPWSVVLELKRDDRPDAKGVPPQGPRGPLTARDVIDMIDPRLKGLRRSAGDTSKDRLRHLEIDEFVYLPSGAGRDEKLYTGRGHETARVYDASAAERHLVDAVGEGGEARRHFLRLRVGSWNEQVVVSLLVRVHTQGGMLVLEVVPHVLGPVLPEFRRADAVAVGEPEGPVRDALRACVDGPAFGVAIGIGALRALPSLGAAVRRWCAAGADEQDGQGPQGPAGNGARHAGARPLPRAVRALRALGARLLPVRTAPPDAPLVSLRELAATDELSLFQEMDVARYTKTLQDRIGEGVREALQDSGYRTDRLEQNITQINNSGVYINEMSGGALATGAQGQATHMEKSTV
>NZ_CP023690.1|WP_150512660.1|5848183_5848579_+|hypothetical-protein
MSDQGNGVSTDGGSHVSINTISGGSQAFGKDGIAVSGSSTTVVASPAHADLLASVRRLRRDLEQGERAAEDEALDAELADVEGEIARTGRSRAERLARVRDRLAQYAPASATAASVTAVLQALAQLPQLPG
>NZ_CP023690.1|WP_150512661.1|5848582_5849368_+|hypothetical-protein
MRVFDDDRQEWVGHEQERQAVALHDRDAARQRAAWRGAVTVLAVCGLAFGTWALGWKDEPEPTAYLLAPQSSANSQESQNSQGAGGDSAERSPTDGPSPVADGLPPGYETLTDARGFRVALPIGWSRTSTAGQGGIGVVNYRNYGASQRLQVYEVSEPTPEASFRDFLDDTKVPKSPSFQKLSLETIDEGQRLTYVTGRIEDEPDVGPWYVVDDRFTAADGKLYAVVGYGSTSTDRALVRQLASNARAWFCPPGSVCQDPG
>NZ_CP023690.1|WP_150512662.1|5849388_5850792_-|MFS-transporter
MSSPALSDAPVKAASPPQPTPLKGITLIVLCACVLVAQSMVAAINLLLPQLTSSSLRPDASELLWTVDAYVIVFAGLLIPAGALGDRYGRKGALLTGLGLFAAGATVSALATTPALLIAGRGVSGAGAALVMPATLSILMRVAAPAEKPRVLAYWALSAGLGGLAGNVGGGLIGAYLPWRALFWIMLPLGALLALAVARTTPRTPVSQEAPALDPFGTLLLITGLVAVLFGIIESPLYGWTSARILSAFAVGAALIAAFVLHALRSKAPLFDPRVFRSRRLSAAALGTAASFFGLFSLFFVNSQYLQYVKGYGAAQAGFAIVPLTVGMVLIPRLAARWSGRPRPVVGGGLLLIGTGLLATSTVDASTPYALYACWLLVISAGTGLSMPALTLGVVTSLPPHQAGLGSGLSTSSREIGAALGVAVTGTVLAHHGGDFAGGMESALRVVGLAVVAVAAVVTLCLGRPRG
>NZ_CP023690.1|WP_150512663.1|5850890_5851865_+|LysR-family-transcriptional-regulator
MTQSSDPESPHPPSPDTPHSPGPDAARRPDVDLNLLIALDALLDEGSVRGAARRLHLSEPAMSRTLGRVRKALGDPVLVRAGRHMVPTPYALAVRAEVGAVLDRARAVFAGPGAQDLRTVERTLTIVGQDSLAATYAPDLFARAAAEAPGVRLRFLSESHLDAPVLREGVADLEVGVIDTTAPEVRVEHFLEDTMMGLVRPGHPLLEGELTPRRFAAADHLTVSRKGRLAGPLDVALAERGLERRVVGNVGTYPASLFILLRTDLVGLATGWMRPLTDELGLVGFPIPLPLPPLRLAMAWHPRHDADPAHAWLRGCVRDLVRRD
>NZ_CP023690.1|WP_150512664.1|5851938_5852310_+|hypothetical-protein
MRQTQDTRWYAVRAPERPWYAVRAPERDEWWWLAPAVGTAAALLGACLRVGDGELPFFWIALTCVPGFLLVAGSWFAPRTRERRGVRVSLAAAGCVLTYLTVKVFMAALYVLAILMWLRQGDG
>NZ_CP023690.1|WP_150512665.1|5852368_5852875_-|hypothetical-protein
MTSFAPGFSGVGTSPQQQHGQSPFQQQGQSQLPPQLQQQLQQFGQQQPFQGLLQQMGQQPGTQPQTQFQVGYAQAVRAPIVPFPGYERAMILLVDGRPVQLLDPSEFAIQSIVFAIQTGQAVRVAYDDRMLVRGVEIEVPRGVIQQHAQQMQQSQQSQQPQQSQQSQF
>NZ_CP023690.1|WP_030668867.1|5853224_5853470_+|helix-turn-helix-transcriptional-regulator
MSEQVHNRLAVVRAERKVSRQSLAEAVGVHYQTIGYIERGQYNPSLDLALKIAKYFGLPVEALFSLEPFRPLTDQLYGRDQ
>NZ_CP023690.1|WP_150512666.1|5853473_5854013_+|hypothetical-protein
MAQQEQLTPHDRRMHALMNRTEGEPLYRTAGRRRAVVVAHIALTVAAVAAWLGTVVGESSWAMWAMLGLLLPWCVATGVINGATRGLLELRPRALDERQRGERERVRARAHQAMTWLLLAAVVGTGLAGFSGVDFKALVFQVTFCVFIAQWLMPLWIAGLTARDEPLDEADDVAAGAAG

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Crispr_ID: NZ_CP023690_10

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_10

6149437-6149543

Orphan

Consensus_repeat	Method
GTCCTCAAACGCCGGACGGGCTGGAT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_10

>merge|NZ_CP023690|10|6149437-6149543|CRISPRCasFinder
GTCCTCAAACGCCGGACGGGCTGGATTTGTCGGCTGTGCGTCGTCGTTCTGTGTCCGTTCCTGCATCGCGCTGGCGCGCTTGTCCTCAAACGCCGGACGGGCTGGAT

>NZ_CP023690|10|10|6149437-6149543|CRISPRCasFinder
GTCCTCAAACGCCGGACGGGCTGGAT	TTGTCGGCTGTGCGTCGTCGTTCTGTGTCCGTTCCTGCATCGCGCTGGCGCGCTT
GTCCTCAAACGCCGGACGGGCTGGAT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150512865.1\|6157331_6158294_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224094
NZ_CP023690.1\|WP_150512869.1\|6162664_6163588_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223674
NZ_CP023690.1\|WP_150512868.1\|6160971_6162594_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173853
NZ_CP023690.1\|WP_150512867.1\|6159350_6160505_+\|dipeptide-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|236898
NZ_CP023690.1\|WP_150515732.1\|6143819_6145073_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|335313
NZ_CP023690.1\|WP_150512860.1\|6148866_6149193_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150515731.1\|6140855_6142880_-\|TPM-domain-containing-protein	unknown	unknown	gnl\|CDD\|377378
NZ_CP023690.1\|WP_150512856.1\|6143125_6143800_+\|SMI1/KNR4-family-protein	unknown	unknown	gnl\|CDD\|379650
NZ_CP023690.1\|WP_150512861.1\|6149788_6152140_+\|ABC-transporter-family-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173866
NZ_CP023690.1\|WP_150512866.1\|6158305_6159358_+\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|223521
NZ_CP023690.1\|WP_150512870.1\|6163580_6164549_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|224094
NZ_CP023690.1\|WP_150512858.1\|6145999_6147928_-\|fumarate-reductase/succinate-dehydrogenase-flavoprotein-subunit	unknown	unknown	gnl\|CDD\|236101
NZ_CP023690.1\|WP_150512864.1\|6156412_6157339_+\|ABC-transporter-permease-subunit	unknown	unknown	gnl\|CDD\|223674
NZ_CP023690.1\|WP_150512862.1\|6152283_6154191_+\|translational-GTPase-TypA	unknown	unknown	gnl\|CDD\|273597
NZ_CP023690.1\|WP_150515729.1\|6136327_6136768_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|340413
NZ_CP023690.1\|WP_150512857.1\|6145214_6146003_-\|succinate-dehydrogenase/fumarate-reductase-iron-sulfur-subunit	unknown	unknown	gnl\|CDD\|237086
NZ_CP023690.1\|WP_150515730.1\|6137429_6140012_+\|SpoIIE-family-protein-phosphatase	unknown	unknown	gnl\|CDD\|369272
NZ_CP023690.1\|WP_150512859.1\|6147977_6148811_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150512863.1\|6154700_6156332_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173853
NZ_CP023690.1\|WP_150512855.1\|6140041_6140755_-\|PspA/IM30-family-protein	unknown	unknown	gnl\|CDD\|224755

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150512865.1\|6157331_6158294_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	8.76573e-88
NZ_CP023690.1\|WP_150512869.1\|6162664_6163588_+\|ABC-transporter-permease-subunit	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	8.48067e-102
NZ_CP023690.1\|WP_150512868.1\|6160971_6162594_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173853	cd00995, PBP2_NikA_DppA_OppA_like, The substrate-binding domain of an ABC-type nickel/oligopeptide-like import system contains the type 2 periplasmic binding fold. This family represents the periplasmic substrate-binding domain of nickel/dipeptide/oligopeptide transport systems, which function in the import of nickel and peptides, and other closely related proteins. The oligopeptide-binding protein OppA is a periplasmic component of an ATP-binding cassette (ABC) transport system OppABCDEF consisting of five subunits: two homologous integral membrane proteins OppB and OppF that form the translocation pore; two homologous nucleotide-binding domains OppD and OppF that drive the transport process through binding and hydrolysis of ATP; and the substrate-binding protein or receptor OppA that determines the substrate specificity of the transport system. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Similar to the ABC-type dipeptide and oligopeptide import systems, nickel transporter is comprised of five subunits NikABCDE: the two pore-forming integral inner membrane proteins NikB and NikC; the two inner membrane-associated proteins with ATPase activity NikD and NikE; and the periplasmic nickel binding NikA, which is the initial nickel receptor that controls the chemotactic response away from nickel. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand binding domains of ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	1.26488e-119
NZ_CP023690.1\|WP_150512867.1\|6159350_6160505_+\|dipeptide-ABC-transporter-ATP-binding-protein	gnl\|CDD\|236898	PRK11308, dppF, dipeptide transporter ATP-binding subunit; Provisional.	1.35011e-158
NZ_CP023690.1\|WP_150515729.1\|6136327_6136768_+\|ATP-binding-protein	gnl\|CDD\|340413	cd16936, HATPase_RsbW-like, Histidine kinase-like ATPase domain of RsbW, an anti sigma-B factor and serine-protein kinase involved in regulating sigma-B during stress in Bacilli, and related domains. This family includes histidine kinase-like ATPase (HATPase) domain of RsbW, an anti sigma-B factor as well as a serine-protein kinase involved in regulating sigma-B during stress in Bacilli. The alternative sigma factor sigma-B is an important regulator of the general stress response of Bacillus cereus and B. subtilis. RsbW is an anti-sigma factor while RsbV is an anti-sigma factor antagonist (anti-anti-sigma factor). RsbW can also act as a kinase on RsbV. In a partner-switching mechanism, RsbW, RsbV, and sigma-B participate as follows: in non-stressed cells, sigma-B is present in an inactive form complexed with RsbW; in this form, sigma-B is unable to bind to RNA polymerase. Under stress, RsbV binds to RsbW, forming an RsbV-RsbW complex, and sigma-B is released to bind to RNA polymerase. RsbW may then act as a kinase on RsbV, phosphorylating a serine residue; RsbW is then released to bind to sigma-B, hence blocking its ability to bind RNA polymerase. A phosphatase then dephosphorylates RsbV so that it can again form a complex with RsbW, leading to the release of sigma-B.	6.29613e-15
NZ_CP023690.1\|WP_150512866.1\|6158305_6159358_+\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|223521	COG0444, DppD, ABC-type dipeptide/oligopeptide/nickel transport system, ATPase component [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	0
NZ_CP023690.1\|WP_150515731.1\|6140855_6142880_-\|TPM-domain-containing-protein	gnl\|CDD\|377378	pfam04536, TPM_phosphatase, TPM domain. This family was first named TPM domain after its founding proteins: TLP18.3, Psb32 and MOLO-1. In Arabidopsis, this domain is called the thylakoid acid phosphatase -TAP - domain and has a Rossmann-like fold. In plants, the family resides in the thylakoid lumen attached to the outer membrane of the chloroplast/plastid. It is active in the photosystem II.	9.56153e-17
NZ_CP023690.1\|WP_150512856.1\|6143125_6143800_+\|SMI1/KNR4-family-protein	gnl\|CDD\|379650	pfam14568, SUKH_6, SMI1-KNR4 cell-wall. Members of this family are related to the SMI1/KNR4-like or SUKH superfamily of proteins.	2.06762e-05
NZ_CP023690.1\|WP_150512861.1\|6149788_6152140_+\|ABC-transporter-family-substrate-binding-protein	gnl\|CDD\|173866	cd08501, PBP2_Lpqw, The substrate-binding domain of mycobacterial lipoprotein Lpqw contains type 2 periplasmic binding fold. LpqW is one of key players in synthesis and transport of the unique components of the mycobacterial cell wall which is a complex structure rich in two related lipoglycans, the phosphatidylinositol mannosides (PIMs) and lipoarabinomannans (LAMs). Lpqw is a highly conserved lipoprotein that transport intermediates from a pathway for mature PIMs production into a pathway for LAMs biosynthesis, thus controlling the relative abundance of these two essential components of cell wall. LpqW is thought to have been adapted by the cell-wall biosynthesis machinery of mycobacteria and other closely related pathogens, evolving to play an important role in PIMs/LAMs biosynthesis. Most of periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the LpqW protein. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand-binding domains from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	2.60221e-90
NZ_CP023690.1\|WP_150512870.1\|6163580_6164549_+\|ABC-transporter-permease-subunit	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.32616e-82
NZ_CP023690.1\|WP_150512858.1\|6145999_6147928_-\|fumarate-reductase/succinate-dehydrogenase-flavoprotein-subunit	gnl\|CDD\|236101	PRK07803, sdhA, succinate dehydrogenase flavoprotein subunit; Reviewed.	0
NZ_CP023690.1\|WP_150512864.1\|6156412_6157339_+\|ABC-transporter-permease-subunit	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	1.68738e-105
NZ_CP023690.1\|WP_150512862.1\|6152283_6154191_+\|translational-GTPase-TypA	gnl\|CDD\|273597	TIGR01394, GTP-binding_protein_TypA/BipA_homolog, GTP-binding protein TypA/BipA. This bacterial (and Arabidopsis) protein, termed TypA or BipA, a GTP-binding protein, is phosphorylated on a tyrosine residue under some cellular conditions. Mutants show altered regulation of some pathways, but the precise function is unknown. [Regulatory functions, Other, Cellular processes, Adaptations to atypical conditions, Protein synthesis, Translation factors].	0
NZ_CP023690.1\|WP_150515732.1\|6143819_6145073_-\|hypothetical-protein	gnl\|CDD\|335313	pfam03403, PAF-AH_p_II, Platelet-activating factor acetylhydrolase, isoform II. Platelet-activating factor acetylhydrolase (PAF-AH) is a subfamily of phospholipases A2, responsible for inactivation of platelet-activating factor through cleavage of an acetyl group. Three known PAF-AHs are the brain heterotrimeric PAF-AH Ib, whose catalytic beta and gamma subunits are aligned in pfam02266, the extracellular, plasma PAF-AH (pPAF-AH), and the intracellular PAF-AH isoform II (PAF-AH II). This family aligns pPAF-AH and PAF-AH II, whose similarity was previously noted.	2.83075e-12
NZ_CP023690.1\|WP_150512857.1\|6145214_6146003_-\|succinate-dehydrogenase/fumarate-reductase-iron-sulfur-subunit	gnl\|CDD\|237086	PRK12386, PRK12386, fumarate reductase iron-sulfur subunit; Provisional.	0
NZ_CP023690.1\|WP_150515730.1\|6137429_6140012_+\|SpoIIE-family-protein-phosphatase	gnl\|CDD\|369272	pfam07228, SpoIIE, Stage II sporulation protein E (SpoIIE). This family contains a number of bacterial stage II sporulation E proteins (EC:3.1.3.16). These are required for formation of a normal polar septum during sporulation. The N-terminal region is hydrophobic and is expected to contain up to 12 membrane-spanning segments.	9.18815e-50
NZ_CP023690.1\|WP_150512863.1\|6154700_6156332_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173853	cd00995, PBP2_NikA_DppA_OppA_like, The substrate-binding domain of an ABC-type nickel/oligopeptide-like import system contains the type 2 periplasmic binding fold. This family represents the periplasmic substrate-binding domain of nickel/dipeptide/oligopeptide transport systems, which function in the import of nickel and peptides, and other closely related proteins. The oligopeptide-binding protein OppA is a periplasmic component of an ATP-binding cassette (ABC) transport system OppABCDEF consisting of five subunits: two homologous integral membrane proteins OppB and OppF that form the translocation pore; two homologous nucleotide-binding domains OppD and OppF that drive the transport process through binding and hydrolysis of ATP; and the substrate-binding protein or receptor OppA that determines the substrate specificity of the transport system. The dipeptide (DppA) and oligopeptide (OppA) binding proteins differ in several ways. The DppA binds dipeptides and some tripeptides and is involved in chemotaxis toward dipeptides, whereas the OppA binds peptides of a wide range of lengths (2-35 amino acid residues) and plays a role in recycling of cell wall peptides, which precludes any involvement in chemotaxis. Similar to the ABC-type dipeptide and oligopeptide import systems, nickel transporter is comprised of five subunits NikABCDE: the two pore-forming integral inner membrane proteins NikB and NikC; the two inner membrane-associated proteins with ATPase activity NikD and NikE; and the periplasmic nickel binding NikA, which is the initial nickel receptor that controls the chemotactic response away from nickel. Most of other periplasmic binding proteins are comprised of only two globular subdomains corresponding to domains I and III of the dipeptide/oligopeptide binding proteins. The structural topology of these domains is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis. Besides transport proteins, the PBP2 superfamily includes the ligand binding domains of ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	1.54527e-111
NZ_CP023690.1\|WP_150512855.1\|6140041_6140755_-\|PspA/IM30-family-protein	gnl\|CDD\|224755	COG1842, PspA, Phage shock protein A (IM30), suppresses sigma54-dependent transcription [Transcription / Signal transduction mechanisms].	1.93287e-19

>NZ_CP023690.1|WP_150512860.1|6148866_6149193_-|hypothetical-protein
MALQDDLTAIQRCVDDLVRTVGRIERQAEPETAGVDFRRVRMDTDHLRESVALLRAAVAPASPPERPAQAPPPPTRPAMVPVPDTPYDSSLWTDSDDEGLGARHRRAP
>NZ_CP023690.1|WP_150512859.1|6147977_6148811_-|hypothetical-protein
MATGTEPHLNKGTAPGGVRHGTRAAIAAAHLRTDRWWLQPAATAAGLFAFVVYSTWRAFANSDYYEAPYVSPFYSPCVADNCEPMRNGPNWEIFGSWWGLSPALLILIFPLGFRLTCYYYRKAYYRGFWASPPACAVAEPHAKYTGETRFPLILQNIHRYFFYAAVPVAGILTYDTVLAFRDEHYEWGHMGLGTLVFLVNIVLIWAYTLSCHSCRHIVGGKLKHFSKHPVRYRMWRWVGWLNGRHMLLAWASLISVALADFYVYLIASGAFDDPALF
>NZ_CP023690.1|WP_150512858.1|6145999_6147928_-|fumarate-reductase/succinate-dehydrogenase-flavoprotein-subunit
MSQVERQQWDVVVVGAGGAGLRAAIEAREQGARTAVICKSLFGKAHTVMAEGGIAAAMANVNSGDNWQVHFRDTLRGGKFLNQWRMAELHAREAPDRVWELETWGALFDRTKDGRISQRNFGGHEYPRLAHVGDRTGLELIRTLQQKIVALQQEDEKEFGDYEARLKVFQECTVTRVLKEGERVSGAFCYERESGRFFVVEAPSVVLATGGIGKSFKVTSNSWEYTGDGHALALLAGAPLLNMEFVQFHPTGMVWPPSVKGILVTESVRGDGGVLRNSDGKRFMFDYVPDVFKEKYAESEEEGDRWYEDPDHNRRPPELLPRDEVARAINSEVKAGRGSPHGGVFLDVSTRMPAEVIRRRLPSMYHQFKELADVDITAEAMEVGPTCHYVMGGVAVDSDTAAARGVPGLFAAGEVAGGMHGSNRLGGNSLSDLLVFGRRAGLHAARYAAELAVRPVVDEPQLDTAAAEALRPFSAEGPSDGATPENPYTLHQELQQTMNDLVGIIRREGEMERALDKLAELRVRARRAGVEGHRQFNPGWHLALDLRNMLLVSECVARAALERTESRGGHTRDDHPGMSREWRRVNLLCRLTDPTGGLAATDPVRGQIDLARVTTDPIRPDLLALFDKEELVKYLAEEELYE
>NZ_CP023690.1|WP_150512857.1|6145214_6146003_-|succinate-dehydrogenase/fumarate-reductase-iron-sulfur-subunit
MSTVASSTAYDAHFRVWRGDTGGGGLQDFTVEVNEGEVVLDIVHRLQATQAPDLAVRWNCKAGKCGSCSAEINGRPRLLCMTRMSVFSREETITVTPLRAFPVVRDLVTDVGFNYTKAREVPAFVPPPGVGPGEYRMMQEDVDRSQEFRKCIECFLCQDTCHVVRDHEENKTAFAGPRFLMRVAELDMHPLDAAADTGLDRKATAQEEHGLGYCNITKCCTEVCPEGIHITDNALIPLKERAVDRKYDPLVWLGNKIRRRGE
>NZ_CP023690.1|WP_150515732.1|6143819_6145073_-|hypothetical-protein
MRTARRSRSMKVLVAAGIAAAVTLGAGAPASARGTESPVRTQPGDPVRPVLPAPTGPHPVGTVTTRLVDHSRPDPWVDSQPYRELMVSVWYPARKTGGGTRPAPYMAPGAAERWDAAAPHGIAKGAVDWAGMRAHARTAAPVDDRGGRRPVLLYSAGANDPRTWGTSLVEEMASRGYVVITVDHTYEAPGVQFPDGSVKGDKPLRDALAEVTDDRSLSELLKKVLDTRVADDKFVLGRLGALPHGLSRAIDRDRVGMLGHSAGGIAAAETMYEDKRVKAAVDLDGTLELNGEPNGTNLTPVARHGVDRPLLLMGRDGSDHTTEPSWRSFWSHTPGWKRDFTLRGSRHQTYTDLAAVLPQTGASRDVIEKNIGTVDPKRAVAAQRAYVASFFDRWLRDRDDHLLDGPSPRFPEVLHVP
>NZ_CP023690.1|WP_150512856.1|6143125_6143800_+|SMI1/KNR4-family-protein
MDGVWAGARERVLAVRERPHWREVFGADWPGGHGHGFRLEPVLTEPEVRAVEQGLGVELPGEYRDFLLQVGAGGAGPDYGLFGHRVTGPDAEPGSGACALPFRPEATDELDGHEGAEPRPDDYADDEALRRDHAAWQARHDTLHASLTDGTLCLSHQGCGYYTLLAVTGPERGTLWDDVRAVGEGVQPVTLQDKPRVTFAQWYLSWLEHAERTAAEGRPRFRAT
>NZ_CP023690.1|WP_150515731.1|6140855_6142880_-|TPM-domain-containing-protein
MPAGAIGSGARAAPADEPVRLDRDGQITDKVGALGDRRAAVADALDRLYDDRRVQLFVAYVRDFSGRPARDWAHATAERNGLGTDDVLLAVATHDRQYAYSAERGGRFSEAQLGEVAATAVEPALRQRDWARAAIGAAGGFGAVLAGEPVPRPAITPGEADPGGGGGGDDGVAGDLVLPVIAVGVAGTFAAVAYRRRKRRFTTRTTPGGWGEGQRLTPLPDLDARAGHLLVETDDAVRTSAEELGFATAQFGEEAARPFAAAVAYAREELTAAFRLRQRLDDAYPEDEATRRRMLDEIVARCTEAGRRLDAEAAAFDELRSLERTAPSALEHAETVLRQVDARALEAESTLKELRTAYAPTSTEAVVGSVAQAKDRLAFAASQLHQARTAVDAADNGTAAVHLRAAEGAVDQAGTFVEGVVRLAGELAEADRRLPGALSETEADLADARGLLTGAGAGTPTADLRGRIARAESVVAEVERARAAGAYDPIDALRRVEEADAALDHALAGARQRESEDDRARTLLGQALLTARSAVAAARDYVTTHRGAVGAEARTRLAEAERHLERAEGPGGPGAPAAALAGAQRADSLARQAQALAERDVRAYGNPYGGGLGAGGRGGGMGGAVLGGIVLGEVLGGLGRGAGGGRGGGGFGGAGPGAFGGGGTRGRMGGGGRF
>NZ_CP023690.1|WP_150512855.1|6140041_6140755_-|PspA/IM30-family-protein
MTKQTVLGRVTQLAKANVHALLDQAEDPQKMLDQLIREYTESIKEAEQAVAATIGDLRLMEQDHGEDQRAAVEWGAKALAASRKADALRMAGSAVEADRFDGLAKVALGRQLRAEKEAKEAEPTIAAQSDVVARLKDGLDSMKIKLTELQSKRDQLVARAKAAQARNRMADAARSLDVLDPTSELSRFEEKVRREEARALGQEELAASSLDAQFEQLESLSDEAEVEARLAALKATT
>NZ_CP023690.1|WP_150515730.1|6137429_6140012_+|SpoIIE-family-protein-phosphatase
MIWQNSPPGSLYDYIKVASFSIGPDGLVDQWSGRAERLFGVPARDAVGKDPIEAFVPPELRPRGHRKMAEILDGREWTGSVPFRLPESAAPLPEPADPLAGPAGPSTEPPAPGAPVREGVAEVYVMPARTADGERSAVCIVVDVRALRQIETDLAASQSIFGQSPFGFLLFGTDLTVQRANRRFAAVFGGAAEDHRGRTVHDYLPRNEADRLQAALRRVLETGEAVTDMQIVGPAPGSSERRHWSINLYRVHSGSGRPIGIAGLGNDVTSRHVAAREAAHARRNLALLNEAGVRIGNSLDLETTARELLDVAVPGFCDLASVDLYQGLLDGDETPPGLADGSAELRRVAFASAVADAPFPEGTGPIDVGSVHRFPFTSPCADALRTARARLIAAGDDCGPTRLTGGLIQSTLAVPMVAHDTVVGLAQFSRTKGSEPFGERDRALAGELAARAAVCIDNARLYRREHERALILQRSLLPPGDPEAAGLDIACRYLPGNAATEVGGDWFDVIELPGHRTALVVGDVMGRGLRAAVTMGELRSAVRTLALLDLEPAEVLSALDEIARGLGNPSGPRRTTARGARDTDDLAEVYLATCVYAVYDAVTRRVTIANAGHLPPVLVEPDESALMLDVPPGMPLGVGGEPFEEVEVDLPEGALLALYTDGLVESRDHPLDEGLNAFVGALTDRGQALEDICDHVLSTLDTHHGEDDIALLMARVQGLPAEHVGDWTLPREPRSVGHARELACARLREWGLDPLVDTAELLVSELVTNALRYGEGEIRLRLLLDRTLVCEVWDAGLVQPRRRRARDTDEGGRGLQLVGLLSAAWGSRRTPRGKTVWFELALPDGDTPPMDAAEALMSLF
>NZ_CP023690.1|WP_150515729.1|6136327_6136768_+|ATP-binding-protein
MDPSLGWEVIGVLDTEGDCAEWDFPADPGAVRTARAVVRKQLGDWDLAPLGDVAVLLVSELVTNSLRYASGPIGVRLVRPKGPLDTLLVEVSDPVPDPPRERVAALDDEGGRGIQLVARSSSRWGTRPGRTGTAGKTVWFELALPG
>NZ_CP023690.1|WP_150512861.1|6149788_6152140_+|ABC-transporter-family-substrate-binding-protein
MPHDRARPPRPVRPKATVRSAVFLAAGVLALPALAGCGADDETSAPAAAQDIAPAARDLVADGGTVKWAVDALPETFNTFQSDADEATSRVAGAVLPSLYRLDARGRVVRNPDFLESAKVVEREPKQVVLYKLNQQAVWSDGREIGADDFAAQWRALSGKDSAYWTARNAGYDRIEKIERGANNLEVRVTFAQPYADWRSLFSPLYPKEVMGTPDSFNDGARTKLKVTAGPFALKDVDRGAGEVTLRRSPRWWGSPAKLDALVLREVPRERRAAALAAGKVDLADVDADEAGRIALAARDKGAPGPLAHGPGARLAPADALRSWAVAHGTDEEAAAVELEARERTGKATRRYADEQTGLRRYTVRKSLEPAYTQLALNGAEGPLADDRVRRAVARALNRAELAETVLKPLGLPASPVGSHLALAGQDAYADNSGALGDQDTAEARALLADAGWTPGGPLKEKYAKDKKEKTAGGEADARGRADGADSGTDGGGDGGGSDDDTYIVGEDDQKPGDTGTSVLAPAPAAAFQQSVLVRQADALTAPGDADKEQRKDPGGPAKKHARKHTEKQAKGGAPGAYAPKGTAAPKTRKGAGGPLAKDGKPLTLRFVLPSGDGSQALRGVADRISRMLERIGVRTEIAKVADESYFKDHIASGQYDLALYSWPASAFPATDARPIFAKPVPAADGSLNVEQNYTRVGTDHIDQLFDQALAELDEGEMRSLVKKADARIWAAAGSIPLYQRPQLVAARARLANAGAFGFATPLYEDIGFLKPGAKPGEKPSDG
>NZ_CP023690.1|WP_150512862.1|6152283_6154191_+|translational-GTPase-TypA
MPTRHDIRNVAIVAHVDHGKTTIVDAMLKQAGAFAAHAAESLDDRMMDSNDLEREKGITILAKNTAVKYHPKDGGEPITINIIDTPGHADFGGEVERGLSMVDAVVLLVDASEGPLPQTRFVLRKALQQRLPVILCINKTDRPDSRIDEVVNETYDLFLDLDADEDQIEFPIVYACGRDGVASLTKPEDGTVPADSTNLEPFFTTLLEHVPAPEYDESAPLQAHVTNLDADNFLGRIALLRVEQGELRKGQTVAWIKRDGSMSNVRITELMMTEALTRKPAEKAGPGDICAVAGIPDIMIGETLADPENPIALPLITVDEPAISMTIGTNTSPLVGRGGTGKGADAKSAVKDRKVTARQVKDRLDRELIGNVSLRVLETGRPDAWEVQGRGELALAILVEQMRREGFELTIGKPQVVTQEIDGKTHEPVERMTIDVPEEHMGAVTQLMGVRKGRMDNMSNHGSGWVRMEFVVPSRGLIGFRTEFLTNTRGTGIAHSIHEGHEPWFGQLQTRNNGSLVADRSGSVTPFAMINLQERGVLFTEPGTEVYEGMIVGENSRSDDMDVNITKEKKLTNMRAASADNTENVVPPRKLSLEQSLEFCRDDECVEVTPEAVRIRKVNLDQRERARAASRAKHG
>NZ_CP023690.1|WP_150512863.1|6154700_6156332_+|ABC-transporter-substrate-binding-protein
MRGARSAKWVGGAIAIALAATACGGGDSGSDDKNRAIDKNGTFVYASGEPQNPLQPANTKEAYGSDVIHTLFTGLVDYTPGTGKLVNMNAESVTPSKDNKTWTVKLKPGWKFHNGEAVTAESYVKAWNWAAYTPNNQTNSSWFADIEGYTDVHPEKGKPKTDKMSGLKVKGANEFTITLTSGIPYYAYKLGYEVFSPLPSGFFKDPKGYGEKPVGNGPYKFASWDHKKSIKVTRYDGYQGPNKAKNGGVTFKNYASSEGAYKDLVSNNVDSMNQVPEGELANYQEDLGDRAINQDYSMIQTIAFARYTKQWKNIDVKVLQGLSMAIDRDTIIKTVLNNTREAATGWVAKDVIGYKAGACGEYCKFDAKKAKDLIKAGGGVPDNKVSIQYNADQPHKGWVTAVCNSIKQSTGVNCVGDPKTDFQADTQTRDAKKVKSMYRSGWVLDYPFNGNFLRDLYGTGVGGNQSGYSNKDFDKLTAKADKAQTTEQSAELYNEAEASLQNSFPSIPLWYGKLQTGASTNVTGVKFDQQAAPIFTEVQVYKK
>NZ_CP023690.1|WP_150512864.1|6156412_6157339_+|ABC-transporter-permease-subunit
MGRYVARRLLQMIPVFIGTTLLIFLMVNVLPGDPVRALWGDKPPDPAQMEAIRHQRGLDLPLWQQYLHYMKNLAVGDLGTNIGGRPVGDILSQAFPVTVRLALLAFGIEMILGIALGMLAGVRRGRVVDNLILVFTLLVISVPVFVLGYIVQTVFGLQLKWTEPTVQDATDITQLILPALVLGSLSLAYVARLTRTSIAENLRADYIRTAVAKGLPKSRIMTRHLLRNSLIPVVTFLGTDIGTLMGGAVVTEGIFNVPGVGNTLYDALARREGQVIVGTVTILVLVYLAASLIVDLLYAVLDPRIRYA
>NZ_CP023690.1|WP_150512865.1|6157331_6158294_+|ABC-transporter-permease-subunit
MPETIKTSSTDGTPDIAADIPATVAEAAGPAPGKPRSLAADAWRDLRRNPFFVISAVLILLLVAIAIFPGWFTSADPNKGDLRNHFQEKPSYTHFFQAEWFGYDTQGRSIYARVLFGARNSITVGILVTLAVSIVGSVLGMLAGYFGGIWDAIISRLTDVFFGIPFLLGTMVVMNAVTDRTVWTVVGALALLGWTQITRVMRGSVITTKHSDYVVAARALGASTWRILIRHILPNAAAPVIVVATIALGGYITAEATLSFLGMGLSDDAISWGSDISDAAKQLRNNPYMLFFPAGMLSLTVLAFIMLGDAVRDALDPKLR
>NZ_CP023690.1|WP_150512866.1|6158305_6159358_+|ATP-binding-cassette-domain-containing-protein
MTTIEKQADVPAPRSGETAPLLEVRDLHVEFHTREGVAKAVNGVNYTVEAGETLAVLGESGSGKSVTAQAIMGILDMPPGRIPQGEVLFRGQDMLKMSNEERRKVRGRKIAMIFQDALSSLNPVLSVGYQLGEMFRVHQGASRKEAKAKAIELMDKVKIPAAKERVDDYPHQFSGGMRQRIMIAMALALEPDLIIADEPTTALDVTVQAQVMDLLAELQREYNMGLILITHDLGVVADVADKIAVMYAGRIVETAPVHELYKRPAHPYTRGLLDSIPRLDQKGQELYAIKGLPPNLLKIPSGCAFNPRCPKAQDICRTEIPTLAPVTERDGGELVGRGSACHFWKETIHG
>NZ_CP023690.1|WP_150512867.1|6159350_6160505_+|dipeptide-ABC-transporter-ATP-binding-protein
MAENLKKDAPDVTDATPNVTEVETVDAATPEEAVAAIEAPVERGEPILQVRNLVKHFPLTQGILIKRQIGAVKAVDGISFDLYQGETLGIVGESGCGKSTVAKLLMTLERATAGEVFYKGQDITKLSGRALKAVRRNIQMVFQDPYTSLNPRMTVGDIIGEPFEIHPEVAPKGDRRRKVQELLDVVGLNPEYINRYPHQFSGGQRQRIGIARGLALNPEIIICDEPVSALDVSVQAQVINLMEKLQDEFNLSYVFIAHDLSIVRHISDRVGVMYLGKMAEIGSDEQIYDHPTHPYTQALLSAVPVPDPEAREGRERIILTGDVPSPANPPSGCRFRTRCWKAQDKCAEEIPLLAIPERFKNADTPAAHESACHFAEEKDVVHAA
>NZ_CP023690.1|WP_150512868.1|6160971_6162594_+|ABC-transporter-substrate-binding-protein
MRGATHAKWAACAAAVALAATACGGGGGGGDSSGVVSSSWGDPQNPLEPANTNEVQGGKVLDMLFRGLKRYDPKTGEAKDMVAESIETEDSQTYTVKVKDGWKFSNGEAVTSKSFVDAWNYGAHLKNNQKGAYFFGYIEGYDKVHPEKGDPSADTLSGLKVVDARTFTVKLSQKFSTWPETLGYPAFAPLPKAFFDDRAGWLAKPVGNGPYSIKSYQKGSKMELRKWDAYSGDDKAENGGVDLRVYTDNNSAYNDLMAGNLDLVDDIPAAQLRNVKNDLGDRYINTPAGIIQTLAFAFYDSKWNKPGAEKVRKGLSMAINREQITETIFQKTRTPAKDWTSPVLGKDGGYSDSLCGDACDYDAEQAKKLVEEGGGIPGGTLKISYNADTGSHKEWVDAVCNSINKALGNNKSCVGNSVGTFADFRSKASQQKLDGAWRAGWQMDYPLIQNFLQPVYYTDAPSNDGKYSSEEFDKLVNEANAETDTGKAVSTFQDAEKVLAKDMAAIPLWYQNGSAGYSDRVSDVALNQFSVPVYAEIKVN
>NZ_CP023690.1|WP_150512869.1|6162664_6163588_+|ABC-transporter-permease-subunit
MGRYVIRRLLQMIPVFFGATLLIFLMVNVMGDPIAGLCGDRKCDPATAAQLKKEFGLDKPVWQQYVTYMGNVFTGDFGTAFNGQKVTELMSTAFPVTIRLTLVAIVFEIVIGISLGVLTGLRRGRPIDTTVLILTLVVISVPTFVTGLLLQLLLGVEWGVIKPAVSAEATVDELIVPGLVLASVSLAYVTRLTRTSIAENRRADYVRTAVAKGLPRRRVVLRHLLRNSLIPVVTFIGTDVGALMGGAIVTERIFNIHGVGFQLYQGILRQSTQTVVGFVTVLVLVFLVANLIVDLLYAVLDPRIRYA
>NZ_CP023690.1|WP_150512870.1|6163580_6164549_+|ABC-transporter-permease-subunit
MPEPQEPDGAIAGTGAGGAMDLATSEATTLAPGAPGGGPTAPARSLWSDAWHDLRRNPVFILSGLIILFLVFISLWPSAIASGDPLDCDLANAQKSSSPGHPFGFDGQGCDVYTRTVYGARASVTVGVCATLGVALLGSVLGGLAGFFGGVWDAILSRITDIFFAIPVVLGGLVLLSVVTSSTVWPVIGFMVLLGWPQISRIARGSVITAKQNDYVQAARALGASNSRMLLRHIAPNAVAPVIVVATIALGTYIALEATLSYLGVGLKPPTVSWGIDISAASAYVRNAPHMLLWPAGALAVTVLAFIMLGDAVRDALDPKLR

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Crispr_ID: NZ_CP023690_11

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023690_11

8036207-8036304

Orphan

Consensus_repeat	Method
TCTCGGCTCCGCTCGAGCAGGGG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023690_11

>merge|NZ_CP023690|11|8036207-8036304|CRISPRCasFinder
TCTCGGCTCCGCTCGAGCAGGGGAGACCCCATCCGAGGACATCCCGGCGCCTTGCGATCGCACGCGCCCCCAAGTTCTCGGCTCCGCTCGAACAGGGG

>NZ_CP023690|11|11|8036207-8036304|CRISPRCasFinder
TCTCGGCTCCGCTCGAGCAGGGG	AGACCCCATCCGAGGACATCCCGGCGCCTTGCGATCGCACGCGCCCCCAAGT
TCTCGGCTCCGCTCGAACAGGGG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023690.1\|WP_150514099.1\|8031463_8034751_-\|transcriptional-regulator	unknown	unknown	gnl\|CDD\|276938
NZ_CP023690.1\|WP_150514100.1\|8034833_8035199_-\|nuclear-transport-factor-2-family-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150515872.1\|8027108_8027642_+\|bacilysin-biosynthesis-protein-BacA	unknown	unknown	gnl\|CDD\|270350
NZ_CP023690.1\|WP_150514105.1\|8038847_8039279_-\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319945
NZ_CP023690.1\|WP_150514106.1\|8039451_8040474_+\|PHB-depolymerase-family-esterase	unknown	unknown	gnl\|CDD\|273828
NZ_CP023690.1\|WP_150515874.1\|8044849_8046865_-\|ATP-binding-cassette-domain-containing-protein	unknown	unknown	gnl\|CDD\|224055
NZ_CP023690.1\|WP_150514095.1\|8025682_8026564_-\|alpha/beta-fold-hydrolase	unknown	unknown	gnl\|CDD\|223669
NZ_CP023690.1\|WP_150514103.1\|8037317_8037803_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|370266
NZ_CP023690.1\|WP_150514110.1\|8047123_8048182_-\|zinc-binding-dehydrogenase	unknown	unknown	gnl\|CDD\|176234
NZ_CP023690.1\|WP_150514104.1\|8037989_8038814_+\|trypsin-like-serine-protease	unknown	unknown	gnl\|CDD\|238113
NZ_CP023690.1\|WP_150514109.1\|8042946_8044890_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|214500
NZ_CP023690.1\|WP_170316546.1\|8030491_8031121_+\|AzlC-family-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|377070
NZ_CP023690.1\|WP_150514097.1\|8029403_8030342_+\|branched-chain-amino-acid-transaminase	unknown	unknown	gnl\|CDD\|181025
NZ_CP023690.1\|WP_150514107.1\|8040585_8041383_+\|3-hydroxybutyrate-dehydrogenase	unknown	unknown	gnl\|CDD\|211705
NZ_CP023690.1\|WP_150514101.1\|8035279_8035705_-\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|378915
NZ_CP023690.1\|WP_030681519.1\|8031117_8031435_+\|AzlD-domain-containing-protein	unknown	unknown	gnl\|CDD\|377512
NZ_CP023690.1\|WP_150515873.1\|8027671_8028937_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023690.1\|WP_150514102.1\|8036411_8036954_+\|FABP-family-protein	unknown	unknown	gnl\|CDD\|378046
NZ_CP023690.1\|WP_150514108.1\|8041453_8042890_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340927
NZ_CP023690.1\|WP_150514096.1\|8028972_8029407_+\|nuclear-transport-factor-2-family-protein	unknown	unknown	gnl\|CDD\|378915

Protein	Function_ID	Function_description	E-value
NZ_CP023690.1\|WP_150514099.1\|8031463_8034751_-\|transcriptional-regulator	gnl\|CDD\|276938	cd15831, BTAD, Bacterial Transcriptional Activation (BTA) domain. The Bacterial Transcriptional Activation (BTA) domain is present in the putative transcriptional regulator Mycobacterium EmbR and the related Streptomyces antibiotic regulatory protein (SARP) family of transcription factors, which includes DnrI and AfsR, among others. Members of this family contain an N-terminal DNA-binding domain, followed by the BTA domain, and many have diverse domains at the C-terminus. EmbR contains an C-terminal forkhead-associated (FHA) domain, which mediates binding to threonine-phosphorylated sites in a sequence-specific manner. The BTA domain of EmbR contains three Tetratricopeptide repeats (TPRs) and two C-terminal helices. The TPR motif typically contains 34 amino acids, and 5 or 6 tandem repeats of the motif generate a right-handed helical structure with an amphipathic channel that is thought to accommodate an alpha-helix of a target protein.	3.0936e-40
NZ_CP023690.1\|WP_170316546.1\|8030491_8031121_+\|AzlC-family-ABC-transporter-permease	gnl\|CDD\|377070	pfam03591, AzlC, AzlC protein.	7.09591e-27
NZ_CP023690.1\|WP_150515872.1\|8027108_8027642_+\|bacilysin-biosynthesis-protein-BacA	gnl\|CDD\|270350	cd13632, PBP2_Aa-PDT_like, Catalytic domain of prephenate dehydratase from Arthrobacter aurescens and similar proteins, subgroup 3; the type 2 periplasmic binding protein fold. Prephenate dehydratase (PDT, EC:4.2.1.51) converts prephenate to phenylpyruvate through dehydration and decarboxylation reactions. PDT plays a key role in the biosynthesis of L-Phe in organisms that utilize the shikimate pathway. PDT is allosterically regulated by L-Phe and other amino acids. The catalytic PDT domain consists of two similar subdomains with a cleft in between, which hosts the highly conserved active site. In gram-postive bacteria and archaea, PDT is a monofunctional enzyme, consisting of a catalytic domain (PDT domain) and a regulatory domain (ACT) (aspartokinase, chorismate mustase domain). In gram-negative bacteria, PDT exists as fusion protein with chorismate mutase (CM), forming a bifunctional enzyme, P-protein (PheA). The CM in the P-protein catalyzes the pericycle isomerization of chorismate to prephenate that serves as a substrate for PDT. The CM and PDT are essentail enzymes for the biosynthesis of aromatic amino acids in microorganisms but are not found in humans. Thus, both CM and PDT can potentially serve as drug targets against microbial pathogens. The PDT domain has the same structural fold as the type 2 periplasmic binding proteins (PBP2), many of which are involved in chemotaxis and uptake of nutrients and other small molecules from the extracellular space as a primary receptor. The PBP2 proteins are typically comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap.	2.45259e-06
NZ_CP023690.1\|WP_150514105.1\|8038847_8039279_-\|VOC-family-protein	gnl\|CDD\|319945	cd08357, VOC_like, uncharacterized subfamily of vicinal oxygen chelate (VOC) familyprotein, glyoxalase I, and type I ring-cleaving dioxygenases. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	1.95184e-67
NZ_CP023690.1\|WP_150514106.1\|8039451_8040474_+\|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].	4.30609e-69
NZ_CP023690.1\|WP_150515874.1\|8044849_8046865_-\|ATP-binding-cassette-domain-containing-protein	gnl\|CDD\|224055	COG1132, MdlB, ABC-type multidrug transport system, ATPase and permease components [Defense mechanisms].	3.70101e-78
NZ_CP023690.1\|WP_150514103.1\|8037317_8037803_+\|hypothetical-protein	gnl\|CDD\|370266	pfam09056, Phospholip_A2_3, Prokaryotic phospholipase A2. The prokaryotic phospholipase A2 domain is predominantly found in bacterial and fungal phospholipases, as well as various hypothetical and putative proteins. It enables the liberation of fatty acids and lysophospholipid by hydrolysing the 2-ester bond of 1,2-diacyl-3-sn-phosphoglycerides. The domain adopts an alpha-helical secondary structure, consisting of five alpha-helices and two helical segments.	6.72976e-46
NZ_CP023690.1\|WP_150514110.1\|8047123_8048182_-\|zinc-binding-dehydrogenase	gnl\|CDD\|176234	cd08273, MDR8, Medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family. This group is a member of the medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, but lacks the zinc-binding sites of the zinc-dependent alcohol dehydrogenases. The medium chain dehydrogenases/reductase (MDR)/zinc-dependent alcohol dehydrogenase-like family, which contains the zinc-dependent alcohol dehydrogenase (ADH-Zn) and related proteins, is a diverse group of proteins related to the first identified member, class I mammalian ADH. MDRs display a broad range of activities and are distinguished from the smaller short chain dehydrogenases (~ 250 amino acids vs. the ~ 350 amino acids of the MDR). The MDR proteins have 2 domains: a C-terminal NAD(P)-binding Rossmann fold domain of a beta-alpha form and an N-terminal catalytic domain with distant homology to GroES. The MDR group contains a host of activities, including the founding alcohol dehydrogenase (ADH), quinone reductase, sorbitol dehydrogenase, formaldehyde dehydrogenase, butanediol DH, ketose reductase, cinnamyl reductase, and numerous others. The zinc-dependent alcohol dehydrogenases (ADHs) catalyze the NAD(P)(H)-dependent interconversion of alcohols to aldehydes or ketones. Active site zinc has a catalytic role, while structural zinc aids in stability. ADH-like proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and generally have 2 tightly bound zinc atoms per subunit. The active site zinc is coordinated by a histidine, two cysteines, and a water molecule. The second zinc seems to play a structural role, affects subunit interactions, and is typically coordinated by 4 cysteines.	2.09672e-128
NZ_CP023690.1\|WP_150514104.1\|8037989_8038814_+\|trypsin-like-serine-protease	gnl\|CDD\|238113	cd00190, Tryp_SPc, Trypsin-like serine protease; Many of these are synthesized as inactive precursor zymogens that are cleaved during limited proteolysis to generate their active forms. Alignment contains also inactive enzymes that have substitutions of the catalytic triad residues.	1.60353e-39
NZ_CP023690.1\|WP_150514109.1\|8042946_8044890_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|214500	smart00065, GAF, Domain present in phytochromes and cGMP-specific phosphodiesterases. Mutations within these domains in PDE6B result in autosomal recessive inheritance of retinitis pigmentosa.	1.73215e-17
NZ_CP023690.1\|WP_150514097.1\|8029403_8030342_+\|branched-chain-amino-acid-transaminase	gnl\|CDD\|181025	PRK07544, PRK07544, branched-chain amino acid aminotransferase; Validated.	4.50144e-139
NZ_CP023690.1\|WP_150514107.1\|8040585_8041383_+\|3-hydroxybutyrate-dehydrogenase	gnl\|CDD\|211705	TIGR01963, D-beta-hydroxybutyrate_dehydrogenase, 3-hydroxybutyrate dehydrogenase. This model represents a subfamily of the short chain dehydrogenases. Characterized members so far as 3-hydroxybutyrate dehydrogenases and are found in species that accumulate ester polmers called polyhydroxyalkanoic acids (PHAs) under certain conditions. Several members of the family are from species not known to accumulate PHAs, including Oceanobacillus iheyensis and Bacillus subtilis. However, polymer formation is not required for there be a role for 3-hydroxybutyrate dehydrogenase; it may be members of this family have the same function in those species.	5.61351e-97
NZ_CP023690.1\|WP_150514101.1\|8035279_8035705_-\|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.	2.1115e-15
NZ_CP023690.1\|WP_150514095.1\|8025682_8026564_-\|alpha/beta-fold-hydrolase	gnl\|CDD\|223669	COG0596, MhpC, Predicted hydrolases or acyltransferases (alpha/beta hydrolase superfamily) [General function prediction only].	2.75879e-10
NZ_CP023690.1\|WP_030681519.1\|8031117_8031435_+\|AzlD-domain-containing-protein	gnl\|CDD\|377512	pfam05437, AzlD, Branched-chain amino acid transport protein (AzlD). This family consists of a number of bacterial and archaeal branched-chain amino acid transport proteins. AzlD is known to be involved in conferring resistance to 4-azaleucine although its exact role is uncertain.	3.06886e-06
NZ_CP023690.1\|WP_150514102.1\|8036411_8036954_+\|FABP-family-protein	gnl\|CDD\|378046	pfam08768, DUF1794, Domain of unknown function (DUF1794). This domain forms a beta barrel structure but the function is unknown. The GO annotation for this protein indicates that the protein has a function in nematode larval development and has a positive regulation on growth rate.	2.90929e-56
NZ_CP023690.1\|WP_150514108.1\|8041453_8042890_+\|MFS-transporter	gnl\|CDD\|340927	cd17369, MFS_ShiA_like, Shikimate transporter and similar proteins of the Major Facilitator Superfamily. This subfamily is composed of Escherichia coli shikimate transporter (ShiA), inner membrane metabolite transport protein YhjE, and other putative metabolite transporters. ShiA is involved in the uptake of shikimate, an aromatic compound involved in siderophore biosynthesis. It has been suggested that YhjE may mediate the uptake of osmoprotectants. The ShiA-like subfamily belongs to the Metazoan Synaptic Vesicle Glycoprotein 2 (SV2) and related small molecule transporter family (SV2-like) of the Major Facilitator Superfamily (MFS) of membrane transport proteins. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	0
NZ_CP023690.1\|WP_150514096.1\|8028972_8029407_+\|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.	1.34814e-06

>NZ_CP023690.1|WP_150514101.1|8035279_8035705_-|nuclear-transport-factor-2-family-protein
MSTHSPETSARATREVIDAYLARLADRDLDGAVRLFSESAEFLAPGSPAVPWSGNRTGHKGVTEFFTTLHEYLQPEEFTVTHIVVDGEQGVIIGHLRDTVKATGKPLTTPFAAHLTVVDGRVARYHLFEDTHALHRAVTDG
>NZ_CP023690.1|WP_150514100.1|8034833_8035199_-|nuclear-transport-factor-2-family-protein
MTSSSGRPSHPAVRAFVDAVNAQDQQALWTVLAKDATVIDVGTERDLHAWVERELFSSHARMEVVRESPDGLCVSARFHNDIWNDIDTAWEFTVSDGVIRRFVTGPDETGPDQSGEAPSGP
>NZ_CP023690.1|WP_150514099.1|8031463_8034751_-|transcriptional-regulator
MSRISEPQEAQTPRESVRIRLLGPVSVEVQGRHVGLGPQQRALLAALALARGPVSTSRLAELLWEGEVPDGAVSSLRTHVLHLRRILEPGSRATSGFAVLVSAGARSNTSYTLQVADEQVDALRFVHLTDQARKAAADGDAATVVALLDEALALWTGPALEGVSDRSFALAETDRLEELRLVAREDRVDALVELGRYEASMAELTPLVREYPLRERLRRQLMLALYRSGRQADALAAYREFYQLLDDEVGIEPGRQLKELHQRVLVGDPALAPERSPAPAAPPAARPVPRQLPPDVASFTGRADQLRELDTLLSRYDTGPGQTLVISSVSGMAGVGKTALAVHWMHRVADRFPDGQLYANLRGHAAEPPTTADEALGQLLRALGVGTGHLPESTDEKAALYRSLLAGKRVLILLDDAAGLEQVRPLLPGSPTCFVVVTSRNDLRGLTAFHDAHRVSLAVFGEDEALALLGRVIGADRVRGEPDAAAEAVRLCGLLPLAVRIVAAHLIGDRHLPIARIVGQLRADRLGELALDQERHTGVRGVLALSYRSLPAPEREALRLLALAPGPEVSVPAAAALTGAAVPATTRLLDQLTARSLLETHRPGRFHLHALVRLFAGERAAAEDAPAVRDEAVGRLLTWYLGTAEQAACQLYGTFYSWYAARPPEPDGSPTAPLAFRNDTAALAWLDDERPALLACAQHAVRHGPRPFAWKSALAVHGHLMEHGRRTDWLRAAHAGLKAAEAEGDDHARAVMHWSLCYVLWELARHEEALEHSARADELFARAGQPVERAGAVLGLAASHRERGALEQAAHDAERALALYREGAQPAGEAWALFLLGRARLDQGDAEAARRHFDEAGARAEASGDQHTVMLSLWGRATVQHALGAMEEAQRLLTRALAVDGRLLATYAAEGALTALAAVCRDAGDPRLALKYAVDALGVTHRTRRRLIEPDALNTIGTVLLRLDDLPGALDHHRRALDAARAACCRRAEVEACLGLAAVHRHLDESREALACTRRALSTARQTGLGLAEGAALTELARVHLALGQTAKAARAVERSVRLHRATGHLPGLTEALEFAAAVERAGAAAAGHPEADTG
>NZ_CP023690.1|WP_030681519.1|8031117_8031435_+|AzlD-domain-containing-protein
MSNDPWIVVGALVVTTFLIKGAGSLVMGDRELPGWFPRFVEYLTPALLAVLVVTQLVGSAGAHGMTFDARLAGFAGALVAWRLKAPVPLVVLVAAAVTAGVRALG
>NZ_CP023690.1|WP_170316546.1|8030491_8031121_+|AzlC-family-ABC-transporter-permease
MPFTVAIFAFGVSFGVLAKGAGFTALAATSMSGLVFVGSSQFAAVSVIVNGGGWAAAAVAGTLLNLRYLVMGFAILPALRGGRARRAVESQLVIEESWAIASDADGRFDRVRLLSSGVVLWLGWVLGTLAGAIGPFRAVDILNYGLDAVSPVLFFLLLAPHLGTARKRSAAATAAVAAAVLTAVAVPDSAIAVACAVAVGWTWWAGRKP
>NZ_CP023690.1|WP_150514097.1|8029403_8030342_+|branched-chain-amino-acid-transaminase
MSGAAPPVPPLDDRDGVIWLDGAFVPWREARLHVLSHGLHYGGSVFEGERVYDGRVFALSEHSARLVASARHMGYALPWTAAELDAVTREVVAAADLTDGYVRPVAWRGGDTLRLVAPDSRVHLAVAAWPWPRIFTEGPRGIRLRTSRWRRPAPDTAPIRAKAAALYAIGALAGQEAEEAGFDDALLLDHRGRLAEATGANLFLVIDGELHTPPPECVLDGITRRTVIGLAGGLGLPVVERHLAPAELDRATEVFLTGTAYEVQPVTGVDGRSFPLGEVGAALTEAYARAVRAGGADRSGYPAPAGAGSDTG
>NZ_CP023690.1|WP_150514096.1|8028972_8029407_+|nuclear-transport-factor-2-family-protein
MGNLDRAALEAAVRRYFEACNKVDRDLFATCLSEEVVHYLAHGMAGPVHGIDPIVERWGADVRANGSHWAVDAVYADEHTRTAVCEWTAFKPRLGKVLRGAEVYRFDDTGLIDEVRIYYASPRDDTRDANELEGFPYADRGFAT
>NZ_CP023690.1|WP_150515873.1|8027671_8028937_+|hypothetical-protein
MRGTHRLHDDLLGEAERLGRGLLPRVNAFRSRQRDDGTVPAPDDADRRALLAVKDEATRWFAGHGRAAQADALAADIEGWLAAGLDTPPHFARSRDALTAPADGDWAAFLAPVRTTNSVPPVGKRLEFFLVRRKEPDALPDLAEHYPHPKNNCQAAVLIAGSAGLADGNCIVFFPENVAAHDKVAEQAYAIFFFSKFRRIHETYAVPSARAVLTPGSVPRASTGMDPEACYQARAVWGYLHDYFHHQGRWPLDRHIKLKMNWFIGLLEELKVDARTALACHADPAVPYADEQIAMILLERMFRYPLDAHAVRNFDAGTGVFLYSWLRERRALTTDRTGLLRLDHDRVIDGLRELVAAVEGMEAAVSTPAEYRAAAKALVRTQLREGAEGDRYAFTDDQRALVRARERLAAAPPPRFAPAEL
>NZ_CP023690.1|WP_150515872.1|8027108_8027642_+|bacilysin-biosynthesis-protein-BacA
MGDIRYLHTLGPTGTNLESAAHLWFQRHGLQNDGQVVLHTSLEDAMASVPRTGAHALVACAVYPELHTLVFGNLLTCRMVDCFLWPTFEMVLAAAPGTHGEPRTVATHPAPAGLVAPTSARQLVTSNAQAAIDCADGKAEGCVTTVVAARAQGLRIVRSFGEVPMVYTVHQMREHGR
>NZ_CP023690.1|WP_150514095.1|8025682_8026564_-|alpha/beta-fold-hydrolase
MTTKLDTYTLDTSGATLTYDVRGGLGDTGADHPVLLLIGSPMDAAGFTTLASHFDDRVVVTYDPRGTGRSVRTDGEGELTPDEHAEDLRRLIEALGFGAVDVFASSGGAVNGLALVTRHPGLVRTLVAHEPPAVRTVPDHEQAWAAVEDIHRTYRREGMGPAMAKFIALTMQKGPLPDGYADAPGPNPADFGLPTEDDGSRDDALLGQNLRGCCGYRPDFDALAAASTRVVIAVGKESEDELAARSGLAIAERLGLAPEVFPSHHGGFLGGEYGQHGEPQPFATKLREVLDTR
>NZ_CP023690.1|WP_150514102.1|8036411_8036954_+|FABP-family-protein
MTQPVPEIPFPDAHRPDGTPAPHAHLAPVTGLLGTWHGLGDGGYPTLEGDFAYAQEVTFSHDGRPFLRYEARAWILDADGGPLRPAARESGWWRLLADGHVEAVISQPTGIVEVATGAAADGTVDLATHQVALTLTAKRVDATRRRYALADDGTLAFTHDLAAVGQPLQHHLSATLRRAH
>NZ_CP023690.1|WP_150514103.1|8037317_8037803_+|hypothetical-protein
MRRRLATLAVSAAALTLGTGLAAAPASAVPADKAQVLSRWTQTDAGSYRAWAAARANQGAWSAYQFNWSTDYCSSSPDNPFGFPFQTACARHDFGYRNYKEMGAFSANKARVDSAFYADLKRVCAAYSGAKKTACDATAWTYYQAVDKLGSVAPTHTKAAA
>NZ_CP023690.1|WP_150514104.1|8037989_8038814_+|trypsin-like-serine-protease
MFSLKSSRRTVARTAAVALAGAACAVLLAGSAEAVVNGKDSTRRYPAMVSIPVTGVDDPTFKGVCGGSLIDAQWVLTAAHCVDPTLVTLDGTVRIGSEWKKSGGTVRSVAKTVSHPGYRNGEGAGPNRDDVALIRLDRPVAEKPLRIADKPGRPGTPTRILGFGTVDDAPDPAEWVFPDRLQELDTRRGAASECAPGYADRTRLCTISQVPKAMACNGDSGGPQLQRDRAGRWELIGVTSGPGAPGVRCSEGPGLYTSAPAYAGWIHRTTGRNG
>NZ_CP023690.1|WP_150514105.1|8038847_8039279_-|VOC-family-protein
MTDLDSPAPRFHLAMPVDDLAAARRFYGGVLGLEEGRSSDAWVDWNLHGHQFVTHLAPERAPRVHNPVDGHDVPVPHFGLLLSVPAFHALAERLRAAGTGFVIEPYVRFAGQKGEQWTMFLLDPAGNALEFKAFADDSQVFAV
>NZ_CP023690.1|WP_150514106.1|8039451_8040474_+|PHB-depolymerase-family-esterase
MTETRAAPHDRRRTGPPVLALALLLVLAFLPGTSPAVAAPHRAGAAALQEVTGFGTNPGQLRMFRYVPDGLAAGRPVVVVLHGCTQNAAGYGTGSGWTELADRWGFSLVLPQQQPVNNISSCFNWFRTGDTTRGLGEAASVAQMVDRHLADLAGDSRRVYVTGLSAGGGMTSVMMAAYPERFAAGGVVAGLPYGCAQAAASPWVCMSSGGGLGPRQWGDRVRAARPGYGGPWPTLTVLHGTADQKVNPVNMTDLTEQWTDVHGADLTADVTDTVAGYPHQVFRGPGGAPAVETYRVTGMGHGQPVDPGTGGERCGTAGPHLLDVGLCAAHRLGRAWGLDT
>NZ_CP023690.1|WP_150514107.1|8040585_8041383_+|3-hydroxybutyrate-dehydrogenase
MTSGPHLNSAARGAPSAAVDLRGRTALVTGGGSGIGRACAAALAAAGAETHVVDIDAAAAKAVADAVGGHAHTADLADAEAIAALPTAVDVLVNSAGLQHVAPLTDFPPARFTLVQQVMVTAPFLLLRQTLPHMYARRWGRAVHISSVHGRRASAFKSAYVAAKHGLEGLSKVTAVEGAPYGVTSNCVSPGYVRTPLVEGQIQDQAAAHRVSDDAVVSDVLLARSPMKRLIEPEEVAAAVLWLCGPHADFVTGTSLPLDGGWTAT
>NZ_CP023690.1|WP_150514108.1|8041453_8042890_+|MFS-transporter
MASLPSTPPPPSPPSTRTSLPRVVAASLVGTTIEWYDFFLYGSAAALVFNDLFFPTADPLTGTLIAFITYAIGFLARPLGGVVFGHYGDKVGRKKLLVVSLLLMGGSTFAMGLLPTYAAIGVGAPVLLTVLRLVQGFALGGEWGGAVLIVSEHGGAAHRGFWASWPQSGAPGGNLLATGVLALLAAVQSEAAFESWGWRIPFLLSGVLVMVGLWIRISVSESPLFLEARAKADAAAARGVKEETPVVEVFRTNWRQVLTAIGTRFGENISYYVLTSFVLVYVTKHLDLPKSTALNAVLIGSAVHFVAIPAWGALSDRVGRRPVTLIGSVGMALWAYVFFALVDSGSFAVITAAVTVGLLLHGAMYGPQAAFISEMFDTRVRYSGASMGSQLASIVAGALAPIIAVHLLKEYDSSAPVALYLCLAAVVTTLTVALARETRGRDLRADAAAPGETDGRGEPGAPGEAGSVPAPVRSGDPS
>NZ_CP023690.1|WP_150514109.1|8042946_8044890_+|helix-turn-helix-domain-containing-protein
MASAHARPGTAPAPDTAGALRELLDLLGRHAPAEQFARPAAAARAAGADRTQLALIEEATDAALAVRRTLDQHRRREAELSALFDTASDLAALSDLDAVLRAIVRRARLLLRTDVAYLTLNDPVEGDTFMRVTDGCASATFQQLRLGMGEGLGGLVAQTARPYASADYRADIRFQHTRAIDTAVGEEGLRGILGVPLRVGSRVIGVLYAADRSPRDFTPDQIALLASLADHAAVAIDSARLLEETRAALVELNAATATAHAQSEALRRAAETHDRLTDIVLRGGDVADVAAEIAALLDGGLVIQDADGTELARVGAAAPTPPARGIAASRSGGRAVPDDGVWVSAVLAGPELLGSIALGGRPDLTDSDRRLFERASLDTALLLLLRRTVAEAEDRVRGELLDDLLTAAHATDPRRAETLALRARRLGVDLTEPTAVLVLHGEPDLRARLATRAIRHARTLRGLAGPLGGHVVLLAPTAEPGPLAARLAAELGEALGAPVTVGAAGPATGPAPLPAAHAEALRCLQALTALGRTGEGASLPDLGFVGVLLGDRTDVAGYVHRVLGPVLDYDTRRGTDLVRTLEAYFDQGASLSRAKDVLHVHVNTVVQRLDRTARLLGADWNSPARALELQLALRLNRLSRSPGPRPA
>NZ_CP023690.1|WP_150515874.1|8044849_8046865_-|ATP-binding-cassette-domain-containing-protein
MLFGGRLRSSWGWTVHEGAQLKTSFLTILRQIPTLVGHTAALGWRADPVALVVVAVAQLGQAAATAFGLLATNRVLVSLFAAGPTAERVQDALPSLIGVAAASALAATLRAVSFAASGGLGPKVERIAALSMLKHVIRVEMEHMERADFHAALDSGQHGQTAARRLIEHTLGIVEAAMALLAVSGVLAVLHPALLPLLVAVIVPKAWGTVRAARRTYESVQVWLEHVRQLGALRRLLISQDAAPELRVHGAGPFLLDQFDGMAAQASDEQTRLAHLEARTDLGTSALSGLTAAVTYGLLAWLLTHGHMPLASGATAVLALTSGTAGLRRLVTNIHHLYEQSLFMTDLIRAREEAKRRAIPATGAAVPEPPAEIAFDRVTFRYPGRDRDALDEVSLSVRKGQVIALVGANGSGKTTLSKLLAGLYLPSSGTVAWDGTDLRALARDDVFSHVALVPQDFQRWPFTARANVAISRPDAIHDSARLDAAAAYADAQRVLCELPHGWDTLCEKGYEGGVDLSGGQWQRIALARAYFRDAGVLICDEPTSSMDPAAEIDAFDKIRALASAEQTIVLVTHRLHSVKEADVIFVLEEGRLVEHGDFATLMATEGPGVFRRLFELQSHQYRTDPVGTDGAAGPHGPDGPLPAGTLDGVPAQPRRARAARPDGAPASGSGG
>NZ_CP023690.1|WP_150514110.1|8047123_8048182_-|zinc-binding-dehydrogenase
MRKTTEVVLPGIVEPEGLSVRRRPAPAPGPGQALLAMEATGVSFAEQQMRRGKYFDQPPFPFVPGYDLVGRVVATGPGVDPALVGGRFAALTKTGGWASHVPVAAADLVPVPESVASADAETLVVNGVTAWQMLHRTAKVRAGDTIVVLGANGGVGSTLAQLARIAGVRVIGTASRRHHDALRRLGVTPVDYRDPELYGRLRGLAPDGVRAVFDHVGGEAVVESFRLLAPGGTLVSYGTASTRDVAGSSKAPVLKLFARLALWQALPNSRHARFYNIWAGRRRADAFRERLRTDLAQVFALLADGSLTAQVAARVPLSRASEALRLAESGTVTGKVVLVPDDTEPHGGPCDK

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NC_004934	Streptomyces violaceoruber strain SANK95570 plasmid pSV2, complete sequence	91196-91227	0	1.0
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP032053	Streptomyces clavuligerus strain F1D-5 plasmid pSCL2, complete sequence	89467-89498	0	1.0
NZ_CP023690_2	2.1\|3332402\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332402-3332433	32	NZ_CP023976	Streptomyces alboflavus strain MDJK44 plasmid pMDJK44.1, complete sequence	57183-57214	1	0.969
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NC_003903	Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence	27857-27888	1	0.969
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NC_003903	Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence	328136-328167	1	0.969
NZ_CP023690_8	8.23\|5546021\|28\|NZ_CP023690\|PILER-CR	5546021-5546048	28	NZ_AP022320	Burkholderia sp. THE68 plasmid BTHE68_p2, complete sequence	58306-58333	4	0.857
NZ_CP023690_8	8.23\|5546021\|28\|NZ_CP023690\|PILER-CR	5546021-5546048	28	NC_016626	Burkholderia sp. YI23 plasmid byi_1p, complete sequence	1753897-1753924	4	0.857
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP026518	Deinococcus sp. NW-56 plasmid unnamed2, complete sequence	282503-282534	5	0.844
NZ_CP023690_8	8.9\|5546323\|40\|NZ_CP023690\|CRT	5546323-5546362	40	NC_004934	Streptomyces violaceoruber strain SANK95570 plasmid pSV2, complete sequence	91188-91227	5	0.875
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	MH744418	Streptomyces phage JustBecause, complete genome	139586-139617	5	0.844
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	MT310898	Streptomyces phage Kela, complete genome	140169-140200	5	0.844
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MT639643	Microbacterium phage FreddieHg, complete genome	13054-13085	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MT818420	Microbacterium phage Gilda, complete genome	13834-13865	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MK737941	Microbacterium phage Rachella, complete genome	13836-13867	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MT522001	Microbacterium phage Karate, complete genome	13255-13286	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MK801732	Microbacterium phage NarutoRun, complete genome	13833-13864	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	NC_047986	Microbacterium phage Krampus, complete genome	13840-13871	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MK801731	Microbacterium phage Anakin, complete genome	13833-13864	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MN497954	Microbacterium phage Hiddenleaf, complete genome	13038-13069	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MH271292	Microbacterium phage AnnaSerena, complete genome	13842-13873	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MT684591	Microbacterium phage Chivey, complete genome	13038-13069	6	0.812
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MT684592	Microbacterium phage Aesir, complete genome	13626-13657	6	0.812
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	CP054927	Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence	67944-67975	6	0.812
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_LR134459	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 17, complete sequence	63326-63357	6	0.812
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP022367	Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence	1565177-1565208	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_016587	Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence	398788-398819	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	CP042595	Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence	269644-269675	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP029777	Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence	240435-240466	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	CP027674	Escherichia coli strain 2014C-3003 plasmid unnamed2, complete sequence	81415-81446	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	LN610585	Pseudomonas phage vB_PaeS_PAO1_Ab20, complete genome	27712-27743	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	KU356689	Pseudomonas phage ZC01, complete genome	28025-28056	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_042115	Pseudomonas phage vB_PaeS_PAO1_Ab19, complete genome	28181-28212	6	0.812
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_026594	Pseudomonas phage vB_PaeS_PAO1_Ab18, complete genome	27723-27754	6	0.812
NZ_CP023690_8	8.9\|5546323\|40\|NZ_CP023690\|CRT	5546323-5546362	40	NZ_CP032053	Streptomyces clavuligerus strain F1D-5 plasmid pSCL2, complete sequence	89467-89506	6	0.85
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP032697	Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525a, complete sequence	258483-258514	6	0.812
NZ_CP023690_8	8.23\|5546021\|28\|NZ_CP023690\|PILER-CR	5546021-5546048	28	NZ_CP011296	Rhodococcus erythropolis strain BG43 plasmid pRLCBG43, complete sequence	24061-24088	6	0.786
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	MG962366	Rhodococcus phage Finch, complete genome	80915-80946	7	0.781
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	MT522003	Microbacterium phage Rie18, complete genome	13187-13218	7	0.781
NZ_CP023690_7	7.2\|5543768\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543768-5543799	32	NZ_CP022195	Yangia pacifica strain YSBP01 plasmid unnamed5, complete sequence	95509-95540	7	0.781
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP032323	Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence	16004-16035	7	0.781
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP022363	Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence	691359-691390	7	0.781
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP007795	Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence	147936-147967	7	0.781
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP032341	Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence	166571-166602	7	0.781
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP032347	Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence	154846-154877	7	0.781
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP012916	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence	73469-73500	7	0.781
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	MN908694	Microbacterium phage RubyRalph, complete genome	27870-27901	7	0.781
NZ_CP023690_7	7.8\|5544134\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544134-5544165	32	NZ_CP014942	Rhodococcus sp. BH4 plasmid, complete sequence	325780-325811	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_008010	Deinococcus geothermalis DSM 11300 plasmid pDGEO01, complete sequence	268203-268234	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP013072	Sphingobium indicum B90A plasmid pSRL2, complete sequence	26798-26829	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP030127	Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence	266249-266280	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_KT070138	Klebsiella pneumoniae strain KP01 plasmid pGES-GZ, complete sequence	11086-11117	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP026223	Aeromonas sp. ASNIH3 plasmid pAER-3367, complete sequence	2838-2869	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP026703	Serratia marcescens strain AR_0027 plasmid unitig_1_pilon, complete sequence	20411-20442	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP013069	Pannonibacter phragmitetus strain 31801 plasmid p.p-1, complete sequence	77899-77930	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP032313	Pannonibacter phragmitetus BB plasmid p.BB_1, complete sequence	273766-273797	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP010421	Azotobacter chroococcum NCIMB 8003 plasmid pAcX50f, complete sequence	299794-299825	7	0.781
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP041045	Paracoccus sp. AK26 plasmid pAK1, complete sequence	387495-387526	7	0.781
NZ_CP023690_8	8.9\|5546323\|40\|NZ_CP023690\|CRT	5546323-5546362	40	NC_003903	Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence	27857-27896	7	0.825
NZ_CP023690_8	8.9\|5546323\|40\|NZ_CP023690\|CRT	5546323-5546362	40	NC_003903	Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence	328128-328167	7	0.825
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_023284	Streptomyces sp. F2 plasmid pFRL4, complete sequence	249507-249538	7	0.781
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_016113	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence	1118505-1118536	7	0.781
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_017585	Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence	694620-694651	7	0.781
NZ_CP023690_8	8.13\|5545957\|32\|NZ_CP023690\|CRISPRCasFinder	5545957-5545988	32	NZ_CP009293	Novosphingobium pentaromativorans US6-1 plasmid pLA4, complete sequence	177374-177405	7	0.781
NZ_CP023690_8	8.14\|5546018\|32\|NZ_CP023690\|CRISPRCasFinder	5546018-5546049	32	NZ_AP022320	Burkholderia sp. THE68 plasmid BTHE68_p2, complete sequence	58304-58335	7	0.781
NZ_CP023690_8	8.14\|5546018\|32\|NZ_CP023690\|CRISPRCasFinder	5546018-5546049	32	NC_016626	Burkholderia sp. YI23 plasmid byi_1p, complete sequence	1753895-1753926	7	0.781
NZ_CP023690_8	8.15\|5546079\|32\|NZ_CP023690\|CRISPRCasFinder	5546079-5546110	32	NC_011371	Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG204, complete sequence	204128-204159	7	0.781
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	MH576962	Streptomyces phage Satis, complete genome	142134-142165	7	0.781
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	MK620894	Streptomyces phage Kradal, complete genome	141797-141828	7	0.781
NZ_CP023690_8	8.17\|5546201\|32\|NZ_CP023690\|CRISPRCasFinder	5546201-5546232	32	NZ_LN832562	Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence	512459-512490	7	0.781
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP020393	Burkholderia vietnamiensis strain FDAARGOS_239 plasmid unnamed, complete sequence	48079-48110	7	0.781
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP009629	Burkholderia vietnamiensis LMG 10929 plasmid pBVB_1, complete sequence	73027-73058	7	0.781
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP029452	Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence	1053719-1053750	7	0.781
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP023071	Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence	1014130-1014161	7	0.781
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_AP022849	Bosea sp. ANAM02 plasmid pANAM02, complete sequence	286265-286296	7	0.781
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP029232	Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence	1055264-1055295	7	0.781
NZ_CP023690_2	2.2\|3332463\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332463-3332494	32	NZ_LT703506	Mycobacterium chimaera strain Mycobacterium chimaera MC045 isolate Mycobacterium chimaera plasmid 2	135485-135516	8	0.75
NZ_CP023690_2	2.2\|3332463\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332463-3332494	32	NC_014811	Mycolicibacterium gilvum Spyr1 plasmid pMSPYR101, complete sequence	67714-67745	8	0.75
NZ_CP023690_2	2.2\|3332463\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332463-3332494	32	NC_008703	Mycobacterium sp. KMS plasmid pMKMS01, complete sequence	79907-79938	8	0.75
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	NZ_CP017753	Cupriavidus sp. USMAHM13 plasmid unnamed1, complete sequence	123446-123477	8	0.75
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1678702-1678733	8	0.75
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	NZ_AP014705	Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence	320085-320116	8	0.75
NZ_CP023690_7	7.2\|5543768\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543768-5543799	32	NZ_CP019319	Tateyamaria omphalii strain DOK1-4 plasmid pDOK1-4-7, complete sequence	1233-1264	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	NZ_KY416992	Escherichia coli strain FAM21805 plasmid unnamed, complete sequence	49173-49204	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	NZ_CP020508	Serratia marcescens strain BWH-35 plasmid unnamed, complete sequence	190161-190192	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	NZ_CP020506	Serratia marcescens strain 95 plasmid unnamed1, complete sequence	3483-3514	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	NZ_CP022697	Citrobacter farmeri strain AUSMDU00008141 plasmid pAUSMDU8141-2, complete sequence	53468-53499	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	NZ_CP017222	Escherichia coli strain FAM21845 plasmid pFAM21845_2, complete sequence	41372-41403	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	NC_019013	Escherichia coli strain G3/10 plasmid pSYM1, complete sequence	6502-6533	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	CP052139	Klebsiella pneumoniae strain F17KP0040 plasmid pF17KP0040-1, complete sequence	93014-93045	8	0.75
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	MN699848	Citrobacter pasteurii strain 175G8 plasmid pCfr-OXA-198, complete sequence	133271-133302	8	0.75
NZ_CP023690_7	7.4\|5543890\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5543890-5543921	32	CP031731	Stenotrophomonas rhizophila strain GA1 plasmid unnamed2, complete sequence	14892-14923	8	0.75
NZ_CP023690_7	7.4\|5543890\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5543890-5543921	32	NZ_CP020041	Streptomyces sp. 3211 isolate 3 plasmid p3211-2, complete sequence	32182-32213	8	0.75
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP030864	Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence	276681-276712	8	0.75
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NC_017588	Thermus thermophilus JL-18 plasmid pTTJL1801, complete sequence	118669-118700	8	0.75
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NZ_CP029357	Azospirillum sp. CFH 70021 plasmid unnamed2	665489-665520	8	0.75
NZ_CP023690_7	7.7\|5544073\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544073-5544104	32	NZ_CP032314	Pannonibacter phragmitetus BB plasmid p.BB_2, complete sequence	61738-61769	8	0.75
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP017077	Novosphingobium resinovorum strain SA1 plasmid pSA2, complete sequence	763804-763835	8	0.75
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP044425	Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence	258862-258893	8	0.75
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_013855	Azospirillum sp. B510 plasmid pAB510a, complete sequence	1014179-1014210	8	0.75
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP014797	Salipiger profundus strain JLT2016 plasmid pTPRO1, complete sequence	60590-60621	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_AP014579	Burkholderia sp. RPE67 plasmid p1, complete sequence	884132-884163	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	96856-96887	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NC_016626	Burkholderia sp. YI23 plasmid byi_1p, complete sequence	742758-742789	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP010858	Marinovum algicola DG 898 plasmid pMaD3	90965-90996	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	LN997843	Streptomyces reticuli genome assembly TUE45, plasmid : II	52673-52704	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_AP017661	Sphingobium cloacae strain JCM 10874 plasmid pSCLO_7, complete sequence	32509-32540	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP010955	Sphingobium sp. YBL2 plasmid 1pYBL2-1, complete sequence	21395-21426	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	2061062-2061093	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP018224	Tardibacter chloracetimidivorans strain JJ-A5 plasmid pHSL3, complete sequence	5163-5194	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP041019	Sphingobium fuliginis ATCC 27551 plasmid pSF2, complete sequence	26734-26765	8	0.75
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP047221	Sphingobium yanoikuyae strain YC-JY1 plasmid unnamed2, complete sequence	37636-37667	8	0.75
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NZ_CP023721	Rhodococcus sp. H-CA8f plasmid unnamed, complete sequence	81705-81736	8	0.75
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NZ_AP022593	Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence	854076-854107	8	0.75
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NZ_CP032687	Rhizobium sp. CCGE531 plasmid pRCCGE531b, complete sequence	133716-133747	8	0.75
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_020061	Rhizobium tropici CIAT 899 plasmid pRtrCIAT899b, complete sequence	132419-132450	8	0.75
NZ_CP023690_8	8.15\|5546079\|32\|NZ_CP023690\|CRISPRCasFinder	5546079-5546110	32	NC_015169	Deinococcus proteolyticus MRP plasmid pDEIPR01, complete sequence	279668-279699	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NC_019849	Sinorhizobium meliloti GR4 plasmid pRmeGR4d, complete sequence	1445360-1445391	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NC_003078	Sinorhizobium meliloti 1021 plasmid pSymB, complete sequence	300135-300166	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP019586	Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymB, complete sequence	302912-302943	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NC_017326	Sinorhizobium meliloti SM11 plasmid pSmeSM11d, complete sequence	1406125-1406156	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021799	Sinorhizobium meliloti strain USDA1106 plasmid psymB, complete sequence	367673-367704	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NC_017323	Sinorhizobium meliloti BL225C plasmid pSINMEB02, complete sequence	996990-997021	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP009146	Sinorhizobium meliloti strain RMO17 plasmid pSymB, complete sequence	1390946-1390977	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021828	Sinorhizobium meliloti strain KH35c plasmid psymB, complete sequence	1553112-1553143	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021802	Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence	23415-23446	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021820	Sinorhizobium meliloti strain M162 plasmid psymB, complete sequence	102512-102543	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021831	Sinorhizobium meliloti strain HM006 plasmid psymB, complete sequence	8186-8217	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021823	Sinorhizobium meliloti strain KH46 plasmid psymB, complete sequence	1667971-1668002	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021814	Sinorhizobium meliloti strain M270 plasmid psymB, complete sequence	1334157-1334188	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021795	Sinorhizobium meliloti strain USDA1157 plasmid psymB, complete sequence	1202265-1202296	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021806	Sinorhizobium meliloti strain T073 plasmid psymB, complete sequence	1254994-1255025	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP021218	Sinorhizobium meliloti RU11/001 plasmid pSymB, complete sequence	1599846-1599877	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP026527	Sinorhizobium meliloti strain AK21 plasmid pSymB, complete sequence	1435048-1435079	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP019484	Sinorhizobium meliloti strain B401 plasmid pSymB, complete sequence	509861-509892	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP019487	Sinorhizobium meliloti strain B399 plasmid pSym, complete sequence	297401-297432	8	0.75
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NC_020560	Sinorhizobium meliloti 2011 plasmid pSymB, complete sequence	300136-300167	8	0.75
NZ_CP023690_8	8.17\|5546201\|32\|NZ_CP023690\|CRISPRCasFinder	5546201-5546232	32	NZ_CP017947	Bosea sp. Tri-49 plasmid unnamed1, complete sequence	448948-448979	8	0.75
NZ_CP023690_8	8.17\|5546201\|32\|NZ_CP023690\|CRISPRCasFinder	5546201-5546232	32	NZ_CP022193	Yangia pacifica strain YSBP01 plasmid unnamed3, complete sequence	139389-139420	8	0.75
NZ_CP023690_8	8.17\|5546201\|32\|NZ_CP023690\|CRISPRCasFinder	5546201-5546232	32	NZ_CP015988	Sphingobium sp. EP60837 plasmid pEP1, complete sequence	112181-112212	8	0.75
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	KT221034	Streptomyces phage SF3, complete genome	18463-18494	8	0.75
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	KT221033	Streptomyces phage SF1, complete genome	36163-36194	8	0.75
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NC_012586	Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence	1241247-1241278	8	0.75
NZ_CP023690_8	8.20\|5546384\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546384-5546415	32	NZ_CP050081	Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b5, complete sequence	281532-281563	8	0.75
NZ_CP023690_8	8.20\|5546384\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546384-5546415	32	NZ_CP049731	Rhizobium leguminosarum strain A1 plasmid pRL12, complete sequence	278072-278103	8	0.75
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	NZ_LR134449	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 7, complete sequence	53374-53405	9	0.719
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	NZ_CP024582	Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence	55498-55529	9	0.719
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	NZ_CP045074	Paracoccus kondratievae strain BJQ0001 plasmid unnamed1, complete sequence	34574-34605	9	0.719
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	KT021004	Thermobifida phage P1312, complete genome	39197-39228	9	0.719
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	CP052389	Klebsiella pneumoniae strain C17KP0052 plasmid pC17KP0052-1	196702-196733	9	0.719
NZ_CP023690_7	7.1\|5543707\|32\|NZ_CP023690\|CRT	5543707-5543738	32	NC_012520	Rhodococcus opacus B4 plasmid pROB01, complete sequence	213725-213756	9	0.719
NZ_CP023690_7	7.3\|5543829\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543829-5543860	32	NZ_CP032346	Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence	977105-977136	9	0.719
NZ_CP023690_7	7.6\|5544012\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544012-5544043	32	NC_015057	Granulicella tundricola MP5ACTX9 plasmid pACIX901, complete sequence	174509-174540	9	0.719
NZ_CP023690_7	7.7\|5544073\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544073-5544104	32	AF271693	Mycobacterium virus Bxb1, complete genome	46344-46375	9	0.719
NZ_CP023690_7	7.7\|5544073\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544073-5544104	32	MK524531	Mycobacterium phage Rutherferd, complete genome	49123-49154	9	0.719
NZ_CP023690_7	7.7\|5544073\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544073-5544104	32	NC_002656	Mycobacterium phage Bxb1, complete genome	46344-46375	9	0.719
NZ_CP023690_7	7.7\|5544073\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544073-5544104	32	MN586021	Arthrobacter phage Beagle, complete genome	19326-19357	9	0.719
NZ_CP023690_7	7.7\|5544073\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544073-5544104	32	MT889394	Arthrobacter phage Odyssey395, complete genome	19348-19379	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP021083	Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence	57550-57581	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP032340	Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence	1323974-1324005	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP012915	Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence	808398-808429	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_017273	Thermus thermophilus SG0.5JP17-16 plasmid pTHTHE1601, complete sequence	12123-12154	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP024424	Paracoccus yeei strain TT13 plasmid pTT13-2, complete sequence	213860-213891	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	403386-403417	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP033321	Azospirillum brasilense strain Cd plasmid p3, complete sequence	415662-415693	9	0.719
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP033315	Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence	472425-472456	9	0.719
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_LR134455	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence	106606-106637	9	0.719
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP020900	Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5d, complete sequence	694037-694068	9	0.719
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NC_021911	Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1f, complete sequence	356853-356884	9	0.719
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP030074	Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence	286146-286177	9	0.719
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NC_012586	Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence	2367368-2367399	9	0.719
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NC_013856	Azospirillum sp. B510 plasmid pAB510b, complete sequence	455269-455300	9	0.719
NZ_CP023690_7	7.12\|5544378\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544378-5544409	32	NZ_CP032325	Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence	263985-264016	9	0.719
NZ_CP023690_7	7.12\|5544378\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544378-5544409	32	NZ_CP022369	Azospirillum sp. TSH58 plasmid TSH58_p05, complete sequence	354976-355007	9	0.719
NZ_CP023690_7	7.12\|5544378\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544378-5544409	32	NZ_CP032342	Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence	310758-310789	9	0.719
NZ_CP023690_7	7.12\|5544378\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544378-5544409	32	NZ_CP033321	Azospirillum brasilense strain Cd plasmid p3, complete sequence	341107-341138	9	0.719
NZ_CP023690_7	7.12\|5544378\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544378-5544409	32	NZ_CP033315	Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence	387415-387446	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	LN907801	unidentified phage genome assembly 2P1, chromosome : 2P1	34487-34518	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389234	UNVERIFIED: Pseudomonas phage F_TK1727sp/MX560 clone contig00002 genomic sequence	8108-8139	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	AY394005	Bacteriophage D3112, complete genome	35124-35155	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	MH719194	Pseudomonas phage Ps60, complete genome	37085-37116	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	JN811560	Pseudomonas phage JBD26, complete genome	35238-35269	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389460	UNVERIFIED: Pseudomonas phage F_MX560sp/Pa1651 clone contig00001 genomic sequence	3661-3692	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_027992	Pseudomonas phage JBD25, complete genome	37241-37272	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389326	UNVERIFIED: Pseudomonas phage F_KK2074sp/Pa1651 clone contig00001 genomic sequence	3659-3690	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389278	UNVERIFIED: Pseudomonas phage Phi05_1400 B clone contig00006 genomic sequence	26019-26050	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389461	UNVERIFIED: Pseudomonas phage F_TK432sp/Pa1651 clone ctg7180000000005 genomic sequence	2563-2594	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	MH643778	Pseudomonas phage YMC12/01/R24, complete genome	34600-34631	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389462	UNVERIFIED: Pseudomonas phage JBD23 clone contig00001 genomic sequence	2574-2605	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	JQ067085	Pseudomonas phage PaMx73, complete genome	33979-34010	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KT968832	Pseudomonas phage YMC11/11/R1836, complete genome	34699-34730	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KJ477077	Pseudomonas phage JD024, complete genome	33702-33733	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_030918	Pseudomonas phage JBD93, complete genome	34028-34059	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_005178	Pseudomonas phage D3112, complete genome	35124-35155	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389464	UNVERIFIED: Pseudomonas phage JBDs5 clone contig00001 genomic sequence	2583-2614	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389459	UNVERIFIED: Pseudomonas phage F_ET309sp/Pa1651 clone contig00001 genomic sequence	34810-34841	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	NC_023700	Pseudomonas phage PA1/KOR/2010, complete genome	31950-31981	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM233689	Pseudomonas phage H70, complete genome	34773-34804	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KU199708	Pseudomonas phage JBD69, complete genome	34348-34379	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	DQ631426	Pseudomonas phage DMS3, complete genome	33899-33930	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	KM389336	UNVERIFIED: Pseudomonas phage JBD58a clone contig00001 genomic sequence	15881-15912	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	JX434031	Pseudomonas phage JBD24, complete genome	34483-34514	9	0.719
NZ_CP023690_8	8.12\|5545896\|32\|NZ_CP023690\|CRISPRCasFinder	5545896-5545927	32	EU272036	Pseudomonas phage MP29, complete genome	34032-34063	9	0.719
NZ_CP023690_8	8.13\|5545957\|32\|NZ_CP023690\|CRISPRCasFinder	5545957-5545988	32	NZ_CP030864	Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence	94066-94097	9	0.719
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP019603	Croceicoccus marinus strain E4A9 plasmid pCME4A9I, complete sequence	529618-529649	9	0.719
NZ_CP023690_8	8.17\|5546201\|32\|NZ_CP023690\|CRISPRCasFinder	5546201-5546232	32	NZ_CP051297	Alicycliphilus denitrificans strain DP3 plasmid pDP3, complete sequence	9214-9245	9	0.719
NZ_CP023690_8	8.17\|5546201\|32\|NZ_CP023690\|CRISPRCasFinder	5546201-5546232	32	NZ_CP051297	Alicycliphilus denitrificans strain DP3 plasmid pDP3, complete sequence	44936-44967	9	0.719
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NC_007974	Cupriavidus metallidurans CH34 megaplasmid, complete sequence	1493204-1493235	9	0.719
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP046333	Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3	278759-278790	9	0.719
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP043499	Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence	1481151-1481182	9	0.719
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NC_021976	Acetobacter pasteurianus 386B plasmid Apa386Bp1, complete sequence	186883-186914	9	0.719
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_CP042810	Acetobacter oryzoeni strain B6 plasmid unnamed2, complete sequence	2981-3012	9	0.719
NZ_CP023690_8	8.19\|5546323\|32\|NZ_CP023690\|CRISPRCasFinder,PILER-CR	5546323-5546354	32	NZ_AP014882	Acetobacter pasteurianus NBRC 101655 plasmid plasmid1 DNA, complete genome	172935-172966	9	0.719
NZ_CP023690_2	2.3\|3332524\|32\|NZ_CP023690\|PILER-CR,CRISPRCasFinder,CRT	3332524-3332555	32	NZ_LR134451	Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence	24324-24355	10	0.688
NZ_CP023690_7	7.2\|5543768\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543768-5543799	32	MH271308	Microbacterium phage Percival, complete genome	39366-39397	10	0.688
NZ_CP023690_7	7.2\|5543768\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543768-5543799	32	NZ_CP029356	Azospirillum sp. CFH 70021 plasmid unnamed1	97206-97237	10	0.688
NZ_CP023690_7	7.2\|5543768\|32\|NZ_CP023690\|CRT,CRISPRCasFinder	5543768-5543799	32	NZ_CP032695	Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence	467569-467600	10	0.688
NZ_CP023690_7	7.4\|5543890\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5543890-5543921	32	NZ_CP015370	Methylobacterium phyllosphaerae strain CBMB27 plasmid CBMB27-p3, complete sequence	25571-25602	10	0.688
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP021405	Celeribacter manganoxidans strain DY25 plasmid pDY25-A, complete sequence	171096-171127	10	0.688
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_020894	Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence	63501-63532	10	0.688
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NC_017766	Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence	63502-63533	10	0.688
NZ_CP023690_7	7.9\|5544195\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544195-5544226	32	NZ_CP034186	Deinococcus sp. S14-83 strain S14-83T plasmid unnamed2, complete sequence	25483-25514	10	0.688
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP007129	Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence	544424-544455	10	0.688
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NC_015178	Acidiphilium multivorum AIU301 plasmid pACMV1, complete sequence	18596-18627	10	0.688
NZ_CP023690_7	7.12\|5544378\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544378-5544409	32	NC_009427	Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence	470426-470457	10	0.688
NZ_CP023690_7	7.10\|5544256\|32\|NZ_CP023690\|CRT,CRISPRCasFinder,PILER-CR	5544256-5544287	32	NZ_CP046053	Methylocystis heyeri strain H2 plasmid unnamed1, complete sequence	85910-85941	11	0.656
NZ_CP023690_8	8.16\|5546140\|32\|NZ_CP023690\|CRISPRCasFinder	5546140-5546171	32	NZ_CP017076	Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence	617211-617242	11	0.656

1. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NC_004934 (Streptomyces violaceoruber strain SANK95570 plasmid pSV2, complete sequence) position: , mismatch: 0, identity: 1.0

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cagcacacgcttcaccgcgtcctgctcgccgc	Protospacer
********************************

2. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP032053 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL2, complete sequence) position: , mismatch: 0, identity: 1.0

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cagcacacgcttcaccgcgtcctgctcgccgc	Protospacer
********************************

3. spacer 2.1|3332402|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP023976 (Streptomyces alboflavus strain MDJK44 plasmid pMDJK44.1, complete sequence) position: , mismatch: 1, identity: 0.969

tggtcccacggtgaatccgggaccatctcgaa	CRISPR spacer
tggtcccacggcgaatccgggaccatctcgaa	Protospacer
***********.********************

4. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NC_003903 (Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence) position: , mismatch: 1, identity: 0.969

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cagcacacgcttcaccgcgtgctgctcgccgc	Protospacer
******************** ***********

5. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NC_003903 (Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence) position: , mismatch: 1, identity: 0.969

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cagcacacgcttcaccgcgtgctgctcgccgc	Protospacer
******************** ***********

6. spacer 8.23|5546021|28|NZ_CP023690|PILER-CR matches to NZ_AP022320 (Burkholderia sp. THE68 plasmid BTHE68_p2, complete sequence) position: , mismatch: 4, identity: 0.857

cggcagtcacttcgcggtctgcggccag	CRISPR spacer
cggcagtcacttcgcggtcgccggcgac	Protospacer
*******************  **** *

7. spacer 8.23|5546021|28|NZ_CP023690|PILER-CR matches to NC_016626 (Burkholderia sp. YI23 plasmid byi_1p, complete sequence) position: , mismatch: 4, identity: 0.857

cggcagtcacttcgcggtctgcggccag	CRISPR spacer
cggcagtcacttcgcggtcgccggcgac	Protospacer
*******************  **** *

8. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP026518 (Deinococcus sp. NW-56 plasmid unnamed2, complete sequence) position: , mismatch: 5, identity: 0.844

ccgcccggtccagcacctgggccagcgtcagg-	CRISPR spacer
ccgcccggtccagcaggtgggcc-gcggcgggc	Protospacer
***************  ****** *** *.**

9. spacer 8.9|5546323|40|NZ_CP023690|CRT matches to NC_004934 (Streptomyces violaceoruber strain SANK95570 plasmid pSV2, complete sequence) position: , mismatch: 5, identity: 0.875

cagcacacgcttcaccgcgtcctgctcgccgcaggaccat-	CRISPR spacer
cagcacacgcttcaccgcgtcctgctcgccgc-gtacggcg	Protospacer
******************************** * ** ..

10. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to MH744418 (Streptomyces phage JustBecause, complete genome) position: , mismatch: 5, identity: 0.844

---atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
cgcgtga---tgaacgcgatcgaggagggcgagga	Protospacer
   .***   ***** *******************

11. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to MT310898 (Streptomyces phage Kela, complete genome) position: , mismatch: 5, identity: 0.844

---atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
cgcgtga---tgaacgcgatcgaggagggcgagga	Protospacer
   .***   ***** *******************

12. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MT639643 (Microbacterium phage FreddieHg, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

13. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MT818420 (Microbacterium phage Gilda, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

14. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MK737941 (Microbacterium phage Rachella, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

15. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MT522001 (Microbacterium phage Karate, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

16. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MK801732 (Microbacterium phage NarutoRun, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

17. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to NC_047986 (Microbacterium phage Krampus, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

18. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MK801731 (Microbacterium phage Anakin, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

19. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MN497954 (Microbacterium phage Hiddenleaf, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

20. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MH271292 (Microbacterium phage AnnaSerena, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

21. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MT684591 (Microbacterium phage Chivey, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

22. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MT684592 (Microbacterium phage Aesir, complete genome) position: , mismatch: 6, identity: 0.812

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgagccg---tcgctgaactcgccgctcagctc	Protospacer
   ***.**   ****** .***************

23. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to CP054927 (Streptomyces fulvissimus strain NA06532 plasmid unnamed1, complete sequence) position: , mismatch: 6, identity: 0.812

tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gtagacgcctctggcggccacacggtgcgctg	Protospacer
   .*****.*.********************

24. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_LR134459 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 17, complete sequence) position: , mismatch: 6, identity: 0.812

---accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
aagaccac---gtcggcctcctcgatggcggcgat	Protospacer
   ***.*   ** ********************

25. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP022367 (Azospirillum sp. TSH58 plasmid TSH58_p02, complete sequence) position: , mismatch: 6, identity: 0.812

accgc-gcggtaggcctcctcgatggcggcgag	CRISPR spacer
-tcgcggcggtaggactcgtcgatggcggcgga	Protospacer
 .*** ******** *** ************..

26. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_016587 (Azospirillum lipoferum 4B plasmid AZO_p4, complete sequence) position: , mismatch: 6, identity: 0.812

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cgccgcggtccagcacctcgcccagcgtcagc	Protospacer
*  * ************* * **********

27. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to CP042595 (Streptomyces albogriseolus strain LBX-2 plasmid pSALBX2, complete sequence) position: , mismatch: 6, identity: 0.812

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gggcccggtgcagctcctgggccagcgtgcgg	Protospacer
  ******* **** *************  **

28. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP029777 (Deinococcus actinosclerus strain Deinococcus actinosclerus SJTR plasmid unnamed3, complete sequence) position: , mismatch: 6, identity: 0.812

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
ccggggcgtccagcacatgggcgagcgtcagg	Protospacer
***    ********* ***** *********

29. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to CP027674 (Escherichia coli strain 2014C-3003 plasmid unnamed2, complete sequence) position: , mismatch: 6, identity: 0.812

ccgcccgg---tccagcacctgggccagcgtcagg	CRISPR spacer
---cctggtcttccaccaccagggccagcgtcagg	Protospacer
   **.**   **** **** **************

30. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to LN610585 (Pseudomonas phage vB_PaeS_PAO1_Ab20, complete genome) position: , mismatch: 6, identity: 0.812

-ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cccgttccg-ccaccacctgggccagcgtctgg	Protospacer
 ***..* * *** **************** **

31. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to KU356689 (Pseudomonas phage ZC01, complete genome) position: , mismatch: 6, identity: 0.812

-ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cccgttccg-ccaccacctgggccagcgtctgg	Protospacer
 ***..* * *** **************** **

32. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_042115 (Pseudomonas phage vB_PaeS_PAO1_Ab19, complete genome) position: , mismatch: 6, identity: 0.812

-ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cccgttccg-ccaccacctgggccagcgtctgg	Protospacer
 ***..* * *** **************** **

33. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_026594 (Pseudomonas phage vB_PaeS_PAO1_Ab18, complete genome) position: , mismatch: 6, identity: 0.812

-ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cccgttctg-ccaccacctgggccagcgtctgg	Protospacer
 ***..* * *** **************** **

34. spacer 8.9|5546323|40|NZ_CP023690|CRT matches to NZ_CP032053 (Streptomyces clavuligerus strain F1D-5 plasmid pSCL2, complete sequence) position: , mismatch: 6, identity: 0.85

cagcacacgcttcaccgcgtcctgctcgccg----caggaccat	CRISPR spacer
cagcacacgcttcaccgcgtcctgctcgccgcgttcggta----	Protospacer
*******************************    *.* *

35. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP032697 (Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525a, complete sequence) position: , mismatch: 6, identity: 0.812

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cacgaggcgcttcacctcgacctgctcgccgc	Protospacer
**  * .********* ** ************

36. spacer 8.23|5546021|28|NZ_CP023690|PILER-CR matches to NZ_CP011296 (Rhodococcus erythropolis strain BG43 plasmid pRLCBG43, complete sequence) position: , mismatch: 6, identity: 0.786

cggcagtcacttcgcggtctgcggccag	CRISPR spacer
gcacacccacttcgccgtctgcggccag	Protospacer
  .** .******** ************

37. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to MG962366 (Rhodococcus phage Finch, complete genome) position: , mismatch: 7, identity: 0.781

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
cgacgtattcggcacgcttggcctcgcgctcc	Protospacer
 ***.* . **** ***** ************

38. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to MT522003 (Microbacterium phage Rie18, complete genome) position: , mismatch: 7, identity: 0.781

---gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
aacgacccg---tcgctgaactcgccgctcagctc	Protospacer
   ** .**   ****** .***************

39. spacer 7.2|5543768|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP022195 (Yangia pacifica strain YSBP01 plasmid unnamed5, complete sequence) position: , mismatch: 7, identity: 0.781

-tgggatgaactggcccgcggcggcggagcgac	CRISPR spacer
ttccggtg-gctggcacgcggcggctgagcgac	Protospacer
 *  *.** .***** ********* *******

40. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032323 (Azospirillum brasilense strain MTCC4035 plasmid p2, complete sequence) position: , mismatch: 7, identity: 0.781

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
agcacgcggaaggccgcctcgatggcgttcag	Protospacer
* *.***** ***** *********** . **

41. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP022363 (Azospirillum sp. TSH58 plasmid TSH58_p03, complete sequence) position: , mismatch: 7, identity: 0.781

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
agcacgcggaaggccgcctcgatggcgttcag	Protospacer
* *.***** ***** *********** . **

42. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP007795 (Azospirillum brasilense strain Az39 plasmid AbAZ39_p2, complete sequence) position: , mismatch: 7, identity: 0.781

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
agcacgcggaaggccgcctcgatggcgttcag	Protospacer
* *.***** ***** *********** . **

43. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032341 (Azospirillum brasilense strain MTCC4038 plasmid p2, complete sequence) position: , mismatch: 7, identity: 0.781

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
agcacgcggaaggccgcctcgatggcgttcag	Protospacer
* *.***** ***** *********** . **

44. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032347 (Azospirillum brasilense strain MTCC4039 plasmid p2, complete sequence) position: , mismatch: 7, identity: 0.781

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
agcacgcggaaggccgcctcgatggcgttcag	Protospacer
* *.***** ***** *********** . **

45. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP012916 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p2, complete sequence) position: , mismatch: 7, identity: 0.781

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
agcacgcggaaggccgcctcgatggcgttcag	Protospacer
* *.***** ***** *********** . **

46. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to MN908694 (Microbacterium phage RubyRalph, complete genome) position: , mismatch: 7, identity: 0.781

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
aacccgtcgtaggcgccctcgatggcggcgaa	Protospacer
* * **. ****** .***************.

47. spacer 7.8|5544134|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP014942 (Rhodococcus sp. BH4 plasmid, complete sequence) position: , mismatch: 7, identity: 0.781

-gacggtcttcgcggcttccctgcgaagtcgac	CRISPR spacer
tgac-accctcgaggcttccctgcgtagtcgat	Protospacer
 *** ..*.*** ************ ******.

48. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_008010 (Deinococcus geothermalis DSM 11300 plasmid pDGEO01, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gttcccggtccagcacctgggccagcgggggc	Protospacer
 . ************************  .*

49. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP013072 (Sphingobium indicum B90A plasmid pSRL2, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gcgcccggtccagcgcctgcgccagcgaattg	Protospacer
 *************.**** *******    *

50. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP030127 (Indioceanicola profundi strain SCSIO 08040 plasmid unnamed1, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
tggcccggtccagcacctggtccaggtccagc	Protospacer
. ****************** ****  .***

51. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_KT070138 (Klebsiella pneumoniae strain KP01 plasmid pGES-GZ, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gctcacggcccagcacctgggccagcttcccg	Protospacer
 * * ***.***************** **  *

52. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP026223 (Aeromonas sp. ASNIH3 plasmid pAER-3367, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gctcacggcccagcacctgggccagcttcccg	Protospacer
 * * ***.***************** **  *

53. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP026703 (Serratia marcescens strain AR_0027 plasmid unitig_1_pilon, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gctcgcggcccagcacctgggccagcttcccg	Protospacer
 * * ***.***************** **  *

54. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP013069 (Pannonibacter phragmitetus strain 31801 plasmid p.p-1, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cgggacggtccagcagctggcccagcgtgggg	Protospacer
* *  ********** **** ******* .**

55. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032313 (Pannonibacter phragmitetus BB plasmid p.BB_1, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cgggacggtccagcagctggcccagcgtgggg	Protospacer
* *  ********** **** ******* .**

56. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP010421 (Azotobacter chroococcum NCIMB 8003 plasmid pAcX50f, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gcggcacgcccagcgccagggccagcgtcagg	Protospacer
 ** *  *.*****.** **************

57. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP041045 (Paracoccus sp. AK26 plasmid pAK1, complete sequence) position: , mismatch: 7, identity: 0.781

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
ccaggcaggccagcaccagggccggcgtcagg	Protospacer
**.  *.* ******** *****.********

58. spacer 8.9|5546323|40|NZ_CP023690|CRT matches to NC_003903 (Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence) position: , mismatch: 7, identity: 0.825

cagcacacgcttcaccgcgtcctgctcgccg----caggaccat	CRISPR spacer
cagcacacgcttcaccgcgtgctgctcgccgcgttcggca----	Protospacer
******************** **********    *.* *

59. spacer 8.9|5546323|40|NZ_CP023690|CRT matches to NC_003903 (Streptomyces coelicolor A3(2) plasmid SCP1, complete sequence) position: , mismatch: 7, identity: 0.825

cagcacacgcttcaccgcgtcctgctcgccg----caggaccat	CRISPR spacer
cagcacacgcttcaccgcgtgctgctcgccgcgttcggca----	Protospacer
******************** **********    *.* *

60. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_023284 (Streptomyces sp. F2 plasmid pFRL4, complete sequence) position: , mismatch: 7, identity: 0.781

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
ccgaccagggagtactcgacgccgacctggcc	Protospacer
***.  ..********** ********** **

61. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_016113 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCAT, complete sequence) position: , mismatch: 7, identity: 0.781

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
ccgtcgaccgagtactcgacgccgacctgacc	Protospacer
***  *.  ********* ********** **

62. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_017585 (Streptomyces cattleya NRRL 8057 = DSM 46488 plasmid pSCATT, complete sequence) position: , mismatch: 7, identity: 0.781

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
ccgtcgaccgagtactcgacgccgacctgacc	Protospacer
***  *.  ********* ********** **

63. spacer 8.13|5545957|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP009293 (Novosphingobium pentaromativorans US6-1 plasmid pLA4, complete sequence) position: , mismatch: 7, identity: 0.781

ccttcccggagcgcgagcacctgggggatcag--	CRISPR spacer
ccgtccccgagcgcgagcacct--gttaccagca	Protospacer
** **** **************  *  *.***

64. spacer 8.14|5546018|32|NZ_CP023690|CRISPRCasFinder matches to NZ_AP022320 (Burkholderia sp. THE68 plasmid BTHE68_p2, complete sequence) position: , mismatch: 7, identity: 0.781

cccggcagtcacttcgcggtctgcggccagat	CRISPR spacer
cgcggcagtcacttcgcggtcgccggcgacga	Protospacer
* *******************  **** * .

65. spacer 8.14|5546018|32|NZ_CP023690|CRISPRCasFinder matches to NC_016626 (Burkholderia sp. YI23 plasmid byi_1p, complete sequence) position: , mismatch: 7, identity: 0.781

cccggcagtcacttcgcggtctgcggccagat	CRISPR spacer
cgcggcagtcacttcgcggtcgccggcgacga	Protospacer
* *******************  **** * .

66. spacer 8.15|5546079|32|NZ_CP023690|CRISPRCasFinder matches to NC_011371 (Rhizobium leguminosarum bv. trifolii WSM2304 plasmid pRLG204, complete sequence) position: , mismatch: 7, identity: 0.781

----gcgtaccccagcagcggccagtggcaggtcga	CRISPR spacer
gacggcgaa----agcggcggccagtggcaggccga	Protospacer
    *** *    ***.***************.***

67. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to MH576962 (Streptomyces phage Satis, complete genome) position: , mismatch: 7, identity: 0.781

---atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
cgtgtggac---aacgcgatcgaggagggcgagga	Protospacer
   .**..*   *** *******************

68. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to MK620894 (Streptomyces phage Kradal, complete genome) position: , mismatch: 7, identity: 0.781

---atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
cgtgtggac---aacgcgatcgaggagggcgagga	Protospacer
   .**..*   *** *******************

69. spacer 8.17|5546201|32|NZ_CP023690|CRISPRCasFinder matches to NZ_LN832562 (Paracoccus aminovorans isolate JCM7685 plasmid IV, complete sequence) position: , mismatch: 7, identity: 0.781

ctgaact--gctcgcgggctgcatgcgctcggct	CRISPR spacer
--ggacctggctcgcggcctgcatgcgcgcggcg	Protospacer
  *.**.  ******** ********** ****

70. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP020393 (Burkholderia vietnamiensis strain FDAARGOS_239 plasmid unnamed, complete sequence) position: , mismatch: 7, identity: 0.781

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cagcacgcgcttccccgcgtcctgagccgcga	Protospacer
******.****** **********  *  **

71. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP009629 (Burkholderia vietnamiensis LMG 10929 plasmid pBVB_1, complete sequence) position: , mismatch: 7, identity: 0.781

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cagcacgcgcttccccgcgtcctgagccgcga	Protospacer
******.****** **********  *  **

72. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP029452 (Sinorhizobium fredii CCBAU 25509 plasmid pSF25509b, complete sequence) position: , mismatch: 7, identity: 0.781

cagcacacg-cttcaccgcgtcctgctcgccgc	CRISPR spacer
-atcgaccgccttctgcgcgtcctgctcgccgc	Protospacer
 * *.  ** ****  *****************

73. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP023071 (Sinorhizobium fredii CCBAU 83666 plasmid pSF83666b, complete sequence) position: , mismatch: 7, identity: 0.781

cagcacacg-cttcaccgcgtcctgctcgccgc	CRISPR spacer
-atcgaccgccttctgcgcgtcctgctcgccgc	Protospacer
 * *.  ** ****  *****************

74. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_AP022849 (Bosea sp. ANAM02 plasmid pANAM02, complete sequence) position: , mismatch: 7, identity: 0.781

cagcacacgctt-caccgcgtcctgctcgccgc	CRISPR spacer
-atcgaacacctgcaccgcgttctgctcgccgc	Protospacer
 * *. **.*.* ********.***********

75. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP029232 (Sinorhizobium fredii CCBAU 45436 plasmid pSF45436b, complete sequence) position: , mismatch: 7, identity: 0.781

cagcacacg-cttcaccgcgtcctgctcgccgc	CRISPR spacer
-atcgaccgccttctgcgcgtcctgctcgccgc	Protospacer
 * *.  ** ****  *****************

76. spacer 2.2|3332463|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LT703506 (Mycobacterium chimaera strain Mycobacterium chimaera MC045 isolate Mycobacterium chimaera plasmid 2) position: , mismatch: 8, identity: 0.75

gccggaactccgacccccggaacg---aagtcgga	CRISPR spacer
tccggaactccgaccacaggaacgcttcggtc---	Protospacer
 ************** * ******    .***

77. spacer 2.2|3332463|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NC_014811 (Mycolicibacterium gilvum Spyr1 plasmid pMSPYR101, complete sequence) position: , mismatch: 8, identity: 0.75

gccggaactccgacccccggaacg---aagtcgga	CRISPR spacer
tccggaactccgaccacaggaacgcttcggtc---	Protospacer
 ************** * ******    .***

78. spacer 2.2|3332463|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NC_008703 (Mycobacterium sp. KMS plasmid pMKMS01, complete sequence) position: , mismatch: 8, identity: 0.75

gccggaactccgacccccggaacg---aagtcgga	CRISPR spacer
tccggaactccgaccacaggaacgcttcggtc---	Protospacer
 ************** * ******    .***

79. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP017753 (Cupriavidus sp. USMAHM13 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
gcatcatcgcggcccgcttcgactcgcgcttg	Protospacer
* *.  .************** ********.

80. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
cggcatccacggcccgctttgcctcgtcatcg	Protospacer
 *.*****.**********.******.  **

81. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP014705 (Methylobacterium aquaticum strain MA-22A plasmid pMaq22A_1p, complete sequence) position: , mismatch: 8, identity: 0.75

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
cgtcgagcgcggcccgcatcgcctcccgcttc	Protospacer
 * *.  ********** ******* ****.*

82. spacer 7.2|5543768|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP019319 (Tateyamaria omphalii strain DOK1-4 plasmid pDOK1-4-7, complete sequence) position: , mismatch: 8, identity: 0.75

tgggatgaactggcccgcggcggcggagcgac	CRISPR spacer
gacgatgaactggccggcggcggcggggccga	Protospacer
 . ************ **********.** .

83. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_KY416992 (Escherichia coli strain FAM21805 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

84. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP020508 (Serratia marcescens strain BWH-35 plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

85. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP020506 (Serratia marcescens strain 95 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

86. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP022697 (Citrobacter farmeri strain AUSMDU00008141 plasmid pAUSMDU8141-2, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

87. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP017222 (Escherichia coli strain FAM21845 plasmid pFAM21845_2, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

88. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NC_019013 (Escherichia coli strain G3/10 plasmid pSYM1, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

89. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to CP052139 (Klebsiella pneumoniae strain F17KP0040 plasmid pF17KP0040-1, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

90. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to MN699848 (Citrobacter pasteurii strain 175G8 plasmid pCfr-OXA-198, complete sequence) position: , mismatch: 8, identity: 0.75

----tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
gaggttcag----ccaggcggcctcacggtgcgctg	Protospacer
    * **.    ** ******* ************

91. spacer 7.4|5543890|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to CP031731 (Stenotrophomonas rhizophila strain GA1 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

gtccgcgccgcccaccgcgggacgattgctct	CRISPR spacer
gaggttgcagcccagcgcgggacgattgctcc	Protospacer
*    .** ***** ****************.

92. spacer 7.4|5543890|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP020041 (Streptomyces sp. 3211 isolate 3 plasmid p3211-2, complete sequence) position: , mismatch: 8, identity: 0.75

gtccgcgccgcccaccgcgggacgattgctct	CRISPR spacer
ctccgcgccgtccaccgctggacgtccgcagt	Protospacer
 *********.******* ***** ..**  *

93. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP030864 (Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
cggatccggcaggcctcctcggtggcggcgag	Protospacer
   .. ***.***********.**********

94. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_017588 (Thermus thermophilus JL-18 plasmid pTTJL1801, complete sequence) position: , mismatch: 8, identity: 0.75

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
aggtcccggtaggcctcctccaaggcggcccg	Protospacer
*   * ************** * ******  *

95. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP029357 (Azospirillum sp. CFH 70021 plasmid unnamed2) position: , mismatch: 8, identity: 0.75

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
tgcggggtgtaggcctcctcgacgtcggcgat	Protospacer
  ** *  **************.* ******

96. spacer 7.7|5544073|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032314 (Pannonibacter phragmitetus BB plasmid p.BB_2, complete sequence) position: , mismatch: 8, identity: 0.75

gaggtgaccaccgcggtgaaccgtgtcgccct	CRISPR spacer
tgggtgaccaccgcggtgacctgtgtcttgcg	Protospacer
 .***************** *.***** . *

97. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP017077 (Novosphingobium resinovorum strain SA1 plasmid pSA2, complete sequence) position: , mismatch: 8, identity: 0.75

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
tcgcccggtccagcaactgcgccagcatgctc	Protospacer
.************** *** ******.*

98. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP044425 (Paracoccus pantotrophus strain DSM 2944 plasmid pPAN2, complete sequence) position: , mismatch: 8, identity: 0.75

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cctgccggtccagcccctcggccagcgccgcc	Protospacer
**  ********** *** ********.*.

99. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_013855 (Azospirillum sp. B510 plasmid pAB510a, complete sequence) position: , mismatch: 8, identity: 0.75

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gcacccggtcgagcgcctgggccagcgcctcc	Protospacer
 *.******* ***.************.*

100. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP014797 (Salipiger profundus strain JLT2016 plasmid pTPRO1, complete sequence) position: , mismatch: 8, identity: 0.75

ccgcccgg---tccagcacctgggccagcgtcagg	CRISPR spacer
---tgcggatttcctgcaactgggccagcgtcagc	Protospacer
   . ***   *** *** ***************

101. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_AP014579 (Burkholderia sp. RPE67 plasmid p1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
gcgtcggcgcggcggcggaaacgcgcggcgtg	Protospacer
*  .** ****************** ** *

102. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
cgcccgccgcgacggcggagacgccgtacagc	Protospacer
 **********.*******.**** * . .**

103. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_016626 (Burkholderia sp. YI23 plasmid byi_1p, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
gcgtcggcgcggcggcggaaacgcgcggcgtg	Protospacer
*  .** ****************** ** *

104. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP010858 (Marinovum algicola DG 898 plasmid pMaD3) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ccttcgccgcggcggcggaatcgctgggtgtc	Protospacer
  ..**************** *** *** * *

105. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to LN997843 (Streptomyces reticuli genome assembly TUE45, plasmid : II) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
gccccgccgcggcggcggccacgcggaggttg	Protospacer
* ****************  ******.*.

106. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_AP017661 (Sphingobium cloacae strain JCM 10874 plasmid pSCLO_7, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ggcccgccgcgtcggccgaaacgtcgccagag	Protospacer
*********** **** ******. *  **.

107. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP010955 (Sphingobium sp. YBL2 plasmid 1pYBL2-1, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ggcccgccgcgtcggccgaaacgtcgccagag	Protospacer
*********** **** ******. *  **.

108. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
cgcccgccgcggcggcggtaccgctgcccgcc	Protospacer
 ***************** * *** *   * *

109. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP018224 (Tardibacter chloracetimidivorans strain JJ-A5 plasmid pHSL3, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ggcccgccgcgtcggccgaaacgtcgccagag	Protospacer
*********** **** ******. *  **.

110. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP041019 (Sphingobium fuliginis ATCC 27551 plasmid pSF2, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ggcccgccgcgtcggccgaaacgtcgccagag	Protospacer
*********** **** ******. *  **.

111. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP047221 (Sphingobium yanoikuyae strain YC-JY1 plasmid unnamed2, complete sequence) position: , mismatch: 8, identity: 0.75

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ggcccgccgcgtcggccgaaacgtcgccagag	Protospacer
*********** **** ******. *  **.

112. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP023721 (Rhodococcus sp. H-CA8f plasmid unnamed, complete sequence) position: , mismatch: 8, identity: 0.75

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
acgcccccggagtgctcgccgccgacctgcct	Protospacer
 **     *****.*****************.

113. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NZ_AP022593 (Mycolicibacterium arabiense strain JCM 18538 plasmid pJCM18538, complete sequence) position: , mismatch: 8, identity: 0.75

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
cgccggaaggcgtactcgccgccgacctccag	Protospacer
*   **.*** ***************** *

114. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP032687 (Rhizobium sp. CCGE531 plasmid pRCCGE531b, complete sequence) position: , mismatch: 8, identity: 0.75

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
accgtgatcgaatactcgtcgccgacctgccc	Protospacer
 * * *.  **.******.*************

115. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_020061 (Rhizobium tropici CIAT 899 plasmid pRtrCIAT899b, complete sequence) position: , mismatch: 8, identity: 0.75

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
accgtgatcgaatactcgtcgccgacctgccc	Protospacer
 * * *.  **.******.*************

116. spacer 8.15|5546079|32|NZ_CP023690|CRISPRCasFinder matches to NC_015169 (Deinococcus proteolyticus MRP plasmid pDEIPR01, complete sequence) position: , mismatch: 8, identity: 0.75

gcgtaccccagcagcggccagtggcaggtcga	CRISPR spacer
ccggcccccagcagcgtccagtgccagggccg	Protospacer
 **  *********** ****** **** * .

117. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NC_019849 (Sinorhizobium meliloti GR4 plasmid pRmeGR4d, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

118. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NC_003078 (Sinorhizobium meliloti 1021 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

119. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP019586 (Sinorhizobium meliloti strain CCMM B554 (FSM-MA) plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

120. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NC_017326 (Sinorhizobium meliloti SM11 plasmid pSmeSM11d, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

121. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021799 (Sinorhizobium meliloti strain USDA1106 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

122. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NC_017323 (Sinorhizobium meliloti BL225C plasmid pSINMEB02, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

123. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP009146 (Sinorhizobium meliloti strain RMO17 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

124. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021828 (Sinorhizobium meliloti strain KH35c plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

125. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021802 (Sinorhizobium meliloti strain USDA1021 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

126. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021820 (Sinorhizobium meliloti strain M162 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

127. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021831 (Sinorhizobium meliloti strain HM006 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

128. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021823 (Sinorhizobium meliloti strain KH46 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

129. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021814 (Sinorhizobium meliloti strain M270 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

130. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021795 (Sinorhizobium meliloti strain USDA1157 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

131. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021806 (Sinorhizobium meliloti strain T073 plasmid psymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

132. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP021218 (Sinorhizobium meliloti RU11/001 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

133. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP026527 (Sinorhizobium meliloti strain AK21 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

134. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP019484 (Sinorhizobium meliloti strain B401 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

135. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP019487 (Sinorhizobium meliloti strain B399 plasmid pSym, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

136. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NC_020560 (Sinorhizobium meliloti 2011 plasmid pSymB, complete sequence) position: , mismatch: 8, identity: 0.75

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
ttcaacgtgaacacgatcaaggagggcgagct	Protospacer
 * *.* ***** *****.***********

137. spacer 8.17|5546201|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP017947 (Bosea sp. Tri-49 plasmid unnamed1, complete sequence) position: , mismatch: 8, identity: 0.75

ctgaactgctcgcgggctgcatgcgctcggct	CRISPR spacer
atgccttgctcgcgtgctgcaggcgctcgaca	Protospacer
 **  .******** ****** *******.*

138. spacer 8.17|5546201|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP022193 (Yangia pacifica strain YSBP01 plasmid unnamed3, complete sequence) position: , mismatch: 8, identity: 0.75

ctgaactgctcgcgggctgcatgcgctcggct	CRISPR spacer
gtgtcgttgtcgcgggctacatgcgctcgcct	Protospacer
 **   *  *********.********** **

139. spacer 8.17|5546201|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP015988 (Sphingobium sp. EP60837 plasmid pEP1, complete sequence) position: , mismatch: 8, identity: 0.75

ctgaactgctcgcgggctgcatgcgctcggct	CRISPR spacer
ccaaactgctcgcgggcggcaagcgccatgca	Protospacer
*..************** *** ****.  **

140. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to KT221034 (Streptomyces phage SF3, complete genome) position: , mismatch: 8, identity: 0.75

cagcacac-gcttcaccgcgtcctgctcgccgc	CRISPR spacer
-gatgtacggcttcaccgcgtactgcgcgccgc	Protospacer
 .....** ************ **** ******

141. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to KT221033 (Streptomyces phage SF1, complete genome) position: , mismatch: 8, identity: 0.75

cagcacac-gcttcaccgcgtcctgctcgccgc	CRISPR spacer
-gatgtacggcttcaccgcgtactgcgcgccgc	Protospacer
 .....** ************ **** ******

142. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NC_012586 (Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence) position: , mismatch: 8, identity: 0.75

cagcacacgcttcacc-gcgtcctgctcgccgc	CRISPR spacer
-atcgaccgccttcccagcgtcctgctcgccgc	Protospacer
 * *.  ***.*. ** ****************

143. spacer 8.20|5546384|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP050081 (Rhizobium leguminosarum bv. trifolii strain 31B plasmid pRL31b5, complete sequence) position: , mismatch: 8, identity: 0.75

gaggtgcagtatccgtacggcatccccgtgat	CRISPR spacer
gagatgcagtatccgtacggcctcgcggaaga	Protospacer
***.***************** ** * * ..

144. spacer 8.20|5546384|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP049731 (Rhizobium leguminosarum strain A1 plasmid pRL12, complete sequence) position: , mismatch: 8, identity: 0.75

gaggtgcagtatccgtacggcatccccgtgat	CRISPR spacer
gagatgcagtatccgtacggcctcgcggaaga	Protospacer
***.***************** ** * * ..

145. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR134449 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 7, complete sequence) position: , mismatch: 9, identity: 0.719

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
cctcatcggcggcccgcttcgccgcgctgacg	Protospacer
   **** *************** ***   *

146. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP024582 (Roseomonas sp. FDAARGOS_362 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
aggatgcggcggccagcatcgcctcgcgctcg	Protospacer
.*.   * ****** ** *************

147. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_CP045074 (Paracoccus kondratievae strain BJQ0001 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
ggccatccgcggtccgcttcgccgtcaggtgg	Protospacer
** *********.********** .  * *

148. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to KT021004 (Thermobifida phage P1312, complete genome) position: , mismatch: 9, identity: 0.719

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
ccgcatccccggcccgctgcgcctcgactacc	Protospacer
  .***** ********* *******  . **

149. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to CP052389 (Klebsiella pneumoniae strain C17KP0052 plasmid pC17KP0052-1) position: , mismatch: 9, identity: 0.719

gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
ccggtacgttcggcgtgctcgccgctcagctg	Protospacer
  * .. ***** .*****************

150. spacer 7.1|5543707|32|NZ_CP023690|CRT matches to NC_012520 (Rhodococcus opacus B4 plasmid pROB01, complete sequence) position: , mismatch: 9, identity: 0.719

gagtcgggttcgctgtgctcgccgctcagctc	CRISPR spacer
caaccggtttcgccgtgctcgccgctccctgc	Protospacer
 *..*** *****.*************  . *

151. spacer 7.3|5543829|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP032346 (Azospirillum brasilense strain MTCC4039 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.719

tacaacgcccccggcggccacacggtgcgctg	CRISPR spacer
ggacgcacccctggcggccacacggggcgccg	Protospacer
 .  .*.****.************* ****.*

152. spacer 7.6|5544012|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_015057 (Granulicella tundricola MP5ACTX9 plasmid pACIX901, complete sequence) position: , mismatch: 9, identity: 0.719

accgcgcggtaggcctcctcgatggcggcgag	CRISPR spacer
ttctcgcggtcggcctccttgatggcgtcaga	Protospacer
 .* ****** ********.******* *...

153. spacer 7.7|5544073|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to AF271693 (Mycobacterium virus Bxb1, complete genome) position: , mismatch: 9, identity: 0.719

gaggtgaccaccgcggtgaaccgtgtcgccct	CRISPR spacer
cgcatggccacctcggtgaaccgtgtcgcggc	Protospacer
 . .**.***** ****************  .

154. spacer 7.7|5544073|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to MK524531 (Mycobacterium phage Rutherferd, complete genome) position: , mismatch: 9, identity: 0.719

gaggtgaccaccgcggtgaaccgtgtcgccct	CRISPR spacer
cgcatggccacctcggtgaaccgtgtcgcggc	Protospacer
 . .**.***** ****************  .

155. spacer 7.7|5544073|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_002656 (Mycobacterium phage Bxb1, complete genome) position: , mismatch: 9, identity: 0.719

gaggtgaccaccgcggtgaaccgtgtcgccct	CRISPR spacer
cgcatggccacctcggtgaaccgtgtcgcggc	Protospacer
 . .**.***** ****************  .

156. spacer 7.7|5544073|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to MN586021 (Arthrobacter phage Beagle, complete genome) position: , mismatch: 9, identity: 0.719

gaggtgaccaccgcggtgaaccgtgtcgccct	CRISPR spacer
ccgcagaccaccgcgctgaaccgtgccgacgc	Protospacer
  *  ********** *********.** * .

157. spacer 7.7|5544073|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to MT889394 (Arthrobacter phage Odyssey395, complete genome) position: , mismatch: 9, identity: 0.719

gaggtgaccaccgcggtgaaccgtgtcgccct	CRISPR spacer
ccgcagaccaccgcgctgaaccgtgccgacgc	Protospacer
  *  ********** *********.** * .

158. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP021083 (Deinococcus ficus strain CC-FR2-10 plasmid pDFI2, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
ggcccgggtccagcacctgggccagctgcgcc	Protospacer
   ** ********************  *.

159. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032340 (Azospirillum brasilense strain MTCC4038 plasmid p1, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
ccagttcgtccagcacataggccagcgtcacc	Protospacer
**. .. ********* *.***********

160. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP012915 (Azospirillum brasilense strain Sp 7 plasmid ABSP7_p1, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
ccagttcgtccagcacataggccagcgtcacc	Protospacer
**. .. ********* *.***********

161. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_017273 (Thermus thermophilus SG0.5JP17-16 plasmid pTHTHE1601, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
tggcccggccctgcacctgggccagggagata	Protospacer
. ******.** ************* *  * .

162. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP024424 (Paracoccus yeei strain TT13 plasmid pTT13-2, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cggccaggtccagcgcctgggccaggcccgct	Protospacer
* *** ********.**********  .*.

163. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gcagcgcgtccagcgcctgggccggcgtcatc	Protospacer
 *. *  *******.********.******

164. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP033321 (Azospirillum brasilense strain Cd plasmid p3, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gcagcgcgtccagcgcctgggccggcgtcatc	Protospacer
 *. *  *******.********.******

165. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP033315 (Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence) position: , mismatch: 9, identity: 0.719

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
gcagcgcgtccagcgcctgggccggcgtcatc	Protospacer
 *. *  *******.********.******

166. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_LR134455 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 13, complete sequence) position: , mismatch: 9, identity: 0.719

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ggcccgccgcgccggcggaatcgcccgtgccg	Protospacer
*********** ******** ***  * .

167. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP020900 (Rhizobium phaseoli Brasil 5 strain Bra5 plasmid pRphaBra5d, complete sequence) position: , mismatch: 9, identity: 0.719

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ttgccggcgcggcggcggaaacgccggtcagg	Protospacer
   *** ***************** **  .*

168. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_021911 (Rhizobium etli bv. mimosae str. Mim1 plasmid pRetMIM1f, complete sequence) position: , mismatch: 9, identity: 0.719

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ttgccggcgcggcggcggaaacgccggtcagg	Protospacer
   *** ***************** **  .*

169. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP030074 (Streptomyces sp. ZFG47 plasmid unnamed1, complete sequence) position: , mismatch: 9, identity: 0.719

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
tgcccgccgcggcggcggaggcgcgcaggtcg	Protospacer
 ******************..**** .*.

170. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_012586 (Sinorhizobium fredii NGR234 plasmid pNGR234b, complete sequence) position: , mismatch: 9, identity: 0.719

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
cgcccgccgcggcggccgaaaggctgcccatc	Protospacer
 *************** **** ** *   . *

171. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_013856 (Azospirillum sp. B510 plasmid pAB510b, complete sequence) position: , mismatch: 9, identity: 0.719

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
ggcccgccgcgccggcggaaccggcgcaccac	Protospacer
*********** ******** **  * .  .*

172. spacer 7.12|5544378|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032325 (Azospirillum brasilense strain MTCC4035 plasmid p4, complete sequence) position: , mismatch: 9, identity: 0.719

gacatcggctcgtggggcgtcactgcggcggc	CRISPR spacer
gcctctatctcgtcgggcggcactgcggcggg	Protospacer
* * ... ***** ***** ***********

173. spacer 7.12|5544378|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP022369 (Azospirillum sp. TSH58 plasmid TSH58_p05, complete sequence) position: , mismatch: 9, identity: 0.719

gacatcggctcgtggggcgtcactgcggcggc	CRISPR spacer
gcctctacctcgtcgggcggcactgcggcggg	Protospacer
* * ... ***** ***** ***********

174. spacer 7.12|5544378|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP032342 (Azospirillum brasilense strain MTCC4038 plasmid p3, complete sequence) position: , mismatch: 9, identity: 0.719

gacatcggctcgtggggcgtcactgcggcggc	CRISPR spacer
gcctctacctcgtcgggcggcactgcggcggg	Protospacer
* * ... ***** ***** ***********

175. spacer 7.12|5544378|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP033321 (Azospirillum brasilense strain Cd plasmid p3, complete sequence) position: , mismatch: 9, identity: 0.719

gacatcggctcgtggggcgtcactgcggcggc	CRISPR spacer
gcctctacctcgtcgggcggcactgcggcggg	Protospacer
* * ... ***** ***** ***********

176. spacer 7.12|5544378|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP033315 (Azospirillum brasilense strain Sp 7 plasmid p3, complete sequence) position: , mismatch: 9, identity: 0.719

gacatcggctcgtggggcgtcactgcggcggc	CRISPR spacer
gcctctacctcgtcgggcggcactgcggcggg	Protospacer
* * ... ***** ***** ***********

177. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to LN907801 (unidentified phage genome assembly 2P1, chromosome : 2P1) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

178. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389234 (UNVERIFIED: Pseudomonas phage F_TK1727sp/MX560 clone contig00002 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggattactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

179. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to AY394005 (Bacteriophage D3112, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

180. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to MH719194 (Pseudomonas phage Ps60, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

181. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to JN811560 (Pseudomonas phage JBD26, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

182. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389460 (UNVERIFIED: Pseudomonas phage F_MX560sp/Pa1651 clone contig00001 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

183. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_027992 (Pseudomonas phage JBD25, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

184. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389326 (UNVERIFIED: Pseudomonas phage F_KK2074sp/Pa1651 clone contig00001 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

185. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389278 (UNVERIFIED: Pseudomonas phage Phi05_1400 B clone contig00006 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

186. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389461 (UNVERIFIED: Pseudomonas phage F_TK432sp/Pa1651 clone ctg7180000000005 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

187. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to MH643778 (Pseudomonas phage YMC12/01/R24, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

188. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389462 (UNVERIFIED: Pseudomonas phage JBD23 clone contig00001 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

189. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to JQ067085 (Pseudomonas phage PaMx73, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

190. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KT968832 (Pseudomonas phage YMC11/11/R1836, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

191. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KJ477077 (Pseudomonas phage JD024, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

192. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_030918 (Pseudomonas phage JBD93, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgactggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

193. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_005178 (Pseudomonas phage D3112, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

194. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389464 (UNVERIFIED: Pseudomonas phage JBDs5 clone contig00001 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

195. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389459 (UNVERIFIED: Pseudomonas phage F_ET309sp/Pa1651 clone contig00001 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

196. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to NC_023700 (Pseudomonas phage PA1/KOR/2010, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

197. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM233689 (Pseudomonas phage H70, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

198. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KU199708 (Pseudomonas phage JBD69, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggattactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

199. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to DQ631426 (Pseudomonas phage DMS3, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

200. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to KM389336 (UNVERIFIED: Pseudomonas phage JBD58a clone contig00001 genomic sequence) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

201. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to JX434031 (Pseudomonas phage JBD24, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

202. spacer 8.12|5545896|32|NZ_CP023690|CRISPRCasFinder matches to EU272036 (Pseudomonas phage MP29, complete genome) position: , mismatch: 9, identity: 0.719

ccgggggaggagtactcgccgccgacctgccc	CRISPR spacer
gcccgaccggactactcgccgccgagctgccg	Protospacer
 *  *.  *** ************* *****

203. spacer 8.13|5545957|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP030864 (Streptomyces globosus strain LZH-48 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.719

ccttcccggagcgcgagcacctgggggatcag	CRISPR spacer
acgtggatgagcgcgagcacctggggcaccat	Protospacer
 * *    ****************** *.**

204. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP019603 (Croceicoccus marinus strain E4A9 plasmid pCME4A9I, complete sequence) position: , mismatch: 9, identity: 0.719

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
atgaacctgaacgcgatcgaggattacaccgc	Protospacer
****.******* **********  .*.  *

205. spacer 8.17|5546201|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP051297 (Alicycliphilus denitrificans strain DP3 plasmid pDP3, complete sequence) position: , mismatch: 9, identity: 0.719

ctgaactgctcgcgggctgcatgcgctcggct	CRISPR spacer
catagtgactcgcgggctggctgcgctcggca	Protospacer
*  *.. .***********  **********

206. spacer 8.17|5546201|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP051297 (Alicycliphilus denitrificans strain DP3 plasmid pDP3, complete sequence) position: , mismatch: 9, identity: 0.719

ctgaactgctcgcgggctgcatgcgctcggct	CRISPR spacer
catagtgactcgcgggctggctgcgctcggca	Protospacer
*  *.. .***********  **********

207. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NC_007974 (Cupriavidus metallidurans CH34 megaplasmid, complete sequence) position: , mismatch: 9, identity: 0.719

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cgaggcctgcgtcaccgcgacctgctcgccga	Protospacer
*.. .* .** ******** ***********

208. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP046333 (Cupriavidus metallidurans strain FDAARGOS_675 plasmid unnamed3) position: , mismatch: 9, identity: 0.719

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
cgaggcctgcgtcaccgcgacctgctcgccga	Protospacer
*.. .* .** ******** ***********

209. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP043499 (Rhizobium grahamii strain BG7 plasmid unnamed, complete sequence) position: , mismatch: 9, identity: 0.719

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
ttcgacggccttcgccgcgtcctgcttgccgc	Protospacer
.   **.  ****.************.*****

210. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NC_021976 (Acetobacter pasteurianus 386B plasmid Apa386Bp1, complete sequence) position: , mismatch: 9, identity: 0.719

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
ccgcacagacttcaccgcgtcctgccgggtct	Protospacer
* ***** .****************. * . .

211. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_CP042810 (Acetobacter oryzoeni strain B6 plasmid unnamed2, complete sequence) position: , mismatch: 9, identity: 0.719

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
ccgcacagacttcaccgcgtcctgccgggtct	Protospacer
* ***** .****************. * . .

212. spacer 8.19|5546323|32|NZ_CP023690|CRISPRCasFinder,PILER-CR matches to NZ_AP014882 (Acetobacter pasteurianus NBRC 101655 plasmid plasmid1 DNA, complete genome) position: , mismatch: 9, identity: 0.719

cagcacacgcttcaccgcgtcctgctcgccgc	CRISPR spacer
ccgcacagacttcaccgcgtcctgccgggtct	Protospacer
* ***** .****************. * . .

213. spacer 2.3|3332524|32|NZ_CP023690|PILER-CR,CRISPRCasFinder,CRT matches to NZ_LR134451 (Tsukamurella tyrosinosolvens strain NCTC13231 plasmid 9, complete sequence) position: , mismatch: 10, identity: 0.688

ggacatccgcggcccgcttcgcctcgcgctcc	CRISPR spacer
ccgcgagggcggcccgcatcgccgcgcgctcg	Protospacer
  .*.   ********* ***** *******

214. spacer 7.2|5543768|32|NZ_CP023690|CRT,CRISPRCasFinder matches to MH271308 (Microbacterium phage Percival, complete genome) position: , mismatch: 10, identity: 0.688

tgggatgaactggcccgcggcggcggagcgac	CRISPR spacer
gcggatggactggcccgcggcgacggcctcga	Protospacer
  *****.**************.***  . .

215. spacer 7.2|5543768|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP029356 (Azospirillum sp. CFH 70021 plasmid unnamed1) position: , mismatch: 10, identity: 0.688

tgggatgaactggcccgcggcggcggagcgac	CRISPR spacer
gctgcagaacaagcccgcggcggcggagctgg	Protospacer
   *  **** .***************** .

216. spacer 7.2|5543768|32|NZ_CP023690|CRT,CRISPRCasFinder matches to NZ_CP032695 (Rhizobium jaguaris strain CCGE525 plasmid pRCCGE525c, complete sequence) position: , mismatch: 10, identity: 0.688

tgggatgaactggcccgcggcggcggagcgac	CRISPR spacer
gaggatgaactggcgcgcggtggcgctcgtgc	Protospacer
 .************ *****.****     .*

217. spacer 7.4|5543890|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP015370 (Methylobacterium phyllosphaerae strain CBMB27 plasmid CBMB27-p3, complete sequence) position: , mismatch: 10, identity: 0.688

gtccgcgccgcccaccgcgggacgattgctct	CRISPR spacer
ccgcgcgccgccagccgcgggacgatcgtcgc	Protospacer
 . ********* .************.*.. .

218. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP021405 (Celeribacter manganoxidans strain DY25 plasmid pDY25-A, complete sequence) position: , mismatch: 10, identity: 0.688

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
ggatcatgtccggcacctgcgccagcgtcaca	Protospacer
  ..*  ****.******* ********** .

219. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_020894 (Streptomyces hygroscopicus subsp. jinggangensis TL01 plasmid pSHJGH1, complete sequence) position: , mismatch: 10, identity: 0.688

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cgctgcggtccagcagctcggccagcgtggtc	Protospacer
*  . ********** ** ********* .

220. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_017766 (Streptomyces hygroscopicus subsp. jinggangensis 5008 plasmid pSHJG1, complete sequence) position: , mismatch: 10, identity: 0.688

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
cgctgcggtccagcagctcggccagcgtggtc	Protospacer
*  . ********** ** ********* .

221. spacer 7.9|5544195|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP034186 (Deinococcus sp. S14-83 strain S14-83T plasmid unnamed2, complete sequence) position: , mismatch: 10, identity: 0.688

ccgcccggtccagcacctgggccagcgtcagg	CRISPR spacer
tgggttcgtccagcaactgggccagcggcaac	Protospacer
. * .. ******** *********** **.

222. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP007129 (Gemmatirosa kalamazoonesis strain KBS708 plasmid 1, complete sequence) position: , mismatch: 10, identity: 0.688

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
tcaccgccgcggcggcggagacgagggtgtag	Protospacer
   ****************.*** *** . .

223. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_015178 (Acidiphilium multivorum AIU301 plasmid pACMV1, complete sequence) position: , mismatch: 10, identity: 0.688

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
atgtcgccgcggcggccggaacgcgggctgcg	Protospacer
.  .************ *.********  *

224. spacer 7.12|5544378|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NC_009427 (Novosphingobium aromaticivorans DSM 12444 plasmid pNL2, complete sequence) position: , mismatch: 10, identity: 0.688

gacatcggctcgtggggcgtcactgcggcggc	CRISPR spacer
ctttgcagctcgtggggcgccacggcggcgat	Protospacer
  .  *.************.*** ******..

225. spacer 7.10|5544256|32|NZ_CP023690|CRT,CRISPRCasFinder,PILER-CR matches to NZ_CP046053 (Methylocystis heyeri strain H2 plasmid unnamed1, complete sequence) position: , mismatch: 11, identity: 0.656

ggcccgccgcggcggcggaaacgcggggaggc	CRISPR spacer
atcccggcacggcggcggaaacgcgcctgctg	Protospacer
. **** *.****************   .

226. spacer 8.16|5546140|32|NZ_CP023690|CRISPRCasFinder matches to NZ_CP017076 (Novosphingobium resinovorum strain SA1 plasmid pSA1, complete sequence) position: , mismatch: 11, identity: 0.656

atgagcctgaacccgatcgaggagggcgagga	CRISPR spacer
caccgcctgaccccgatcgaggcgggccgtct	Protospacer
    ****** *********** **** .

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

570687 : 619172

Bacillus_phage(40.0%)

holin,plate,tail,tRNA

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_150508896.1\|570687_571503_-\|tRNA	tRNA-dependent cyclodipeptide synthase	NA	NA	NA	NA
WP_150508897.1\|571969_572629_+	DUF4360 domain-containing protein	NA	NA	NA	NA
WP_150508898.1\|572779_573439_-	DUF1707 domain-containing protein	NA	NA	NA	NA
WP_150508899.1\|573918_576492_+	hypothetical protein	NA	NA	NA	NA
WP_150508900.1\|576532_576901_-	heavy metal-binding domain-containing protein	NA	NA	NA	NA
WP_170316326.1\|576944_577457_-	NUDIX domain-containing protein	NA	NA	NA	NA
WP_150515267.1\|577770_578775_+	serine hydrolase	G1DAH7	Mycobacterium_virus	2.2e-21	27.6
WP_150508902.1\|578863_579331_+	DUF1801 domain-containing protein	NA	NA	NA	NA
WP_150508903.1\|579356_580157_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_150508904.1\|580214_580685_-	hypothetical protein	NA	NA	NA	NA
WP_150508905.1\|580807_581845_-	sulfotransferase	NA	NA	NA	NA
WP_150508906.1\|581965_583444_-	MFS transporter	NA	NA	NA	NA
WP_150508907.1\|583676_584681_+	YdcF family protein	NA	NA	NA	NA
WP_150508908.1\|584735_585659_-	LLM class flavin-dependent oxidoreductase	NA	NA	NA	NA
WP_150508909.1\|585769_586219_+	MerR family transcriptional regulator	NA	NA	NA	NA
WP_150508910.1\|586506_587253_+	VCBS repeat-containing protein	NA	NA	NA	NA
WP_170316612.1\|587465_588065_+	response regulator transcription factor	NA	NA	NA	NA
WP_150508912.1\|588225_588903_+	DUF4255 domain-containing protein	NA	NA	NA	NA
WP_150508913.1\|588899_590921_+	AAA family ATPase	A0A0R6PCP6	Moraxella_phage	2.3e-22	34.1
WP_150508914.1\|590952_592356_-	hydrolase	NA	NA	NA	NA
WP_150508915.1\|592661_594257_+\|tail	phage tail sheath subtilisin-like domain-containing protein	J9PVC2	Bacillus_phage	6.7e-65	32.0
WP_150508916.1\|594365_594809_+\|tail	phage tail protein	NA	NA	NA	NA
WP_150508917.1\|594808_595315_+	hypothetical protein	NA	NA	NA	NA
WP_170316327.1\|595311_595470_+	hypothetical protein	NA	NA	NA	NA
WP_150508918.1\|596279_597065_-	hypothetical protein	NA	NA	NA	NA
WP_150508919.1\|598416_598905_+	hypothetical protein	NA	NA	NA	NA
WP_150508920.1\|598973_599396_+\|tail	phage tail protein	NA	NA	NA	NA
WP_150508921.1\|599425_600145_+	LysM peptidoglycan-binding domain-containing protein	NA	NA	NA	NA
WP_150508922.1\|600144_602052_+	VgrG-related protein	NA	NA	NA	NA
WP_150508923.1\|602106_602559_+	GPW/gp25 family protein	A0A1D7SP91	Cyanophage	3.0e-10	31.6
WP_150508924.1\|602558_604517_+\|plate	putative baseplate assembly protein	NA	NA	NA	NA
WP_150508925.1\|604545_605103_+\|tail	phage tail protein	NA	NA	NA	NA
WP_170316328.1\|605099_606554_+	zinc ribbon domain-containing protein	NA	NA	NA	NA
WP_170316329.1\|606846_608745_+	FAD/NAD(P)-binding protein	NA	NA	NA	NA
WP_150508928.1\|608777_609554_+	L-iditol 2-dehydrogenase	NA	NA	NA	NA
WP_150508929.1\|609588_610959_+	glycosyltransferase	NA	NA	NA	NA
WP_150508930.1\|610970_612167_+	MFS transporter	NA	NA	NA	NA
WP_150508931.1\|612163_612970_+	acetoacetate decarboxylase family protein	NA	NA	NA	NA
WP_150508932.1\|612966_613524_+	5'(3')-deoxyribonucleotidase	NA	NA	NA	NA
WP_150508933.1\|613579_613993_-	ANTAR domain-containing protein	NA	NA	NA	NA
WP_150515268.1\|614094_614445_-	response regulator	W8CYM9	Bacillus_phage	4.5e-06	35.5
WP_150508934.1\|615006_615234_-	DUF5133 domain-containing protein	NA	NA	NA	NA
WP_150508935.1\|615432_616653_+	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_150508936.1\|616717_616900_-	CsbD family protein	NA	NA	NA	NA
WP_150515269.1\|617351_617993_-	DUF4157 domain-containing protein	NA	NA	NA	NA
WP_150508937.1\|618410_618614_+	hypothetical protein	NA	NA	NA	NA
WP_150508938.1\|618800_619172_+\|holin	phage holin family protein	NA	NA	NA	NA

DBSCAN-SWA_2

1802286 : 1811046

Streptomyces_phage(57.14%)

capsid,portal,terminase

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_150509747.1\|1802286_1803243_-\|capsid	phage major capsid protein	A0A2H4J273	uncultured_Caudovirales_phage	1.1e-35	36.9
WP_150509748.1\|1803263_1803920_-	hypothetical protein	NA	NA	NA	NA
WP_150509749.1\|1803983_1804799_-	hypothetical protein	A0A076G757	Mycobacterium_phage	3.3e-07	26.5
WP_150509750.1\|1804776_1806246_-\|portal	phage portal protein	A0A2H4JAT8	uncultured_Caudovirales_phage	1.0e-75	41.6
WP_150509751.1\|1806242_1808012_-\|terminase	terminase	A0A0K1Y9I5	Streptomyces_phage	7.8e-131	46.4
WP_150515368.1\|1807983_1808424_-	hypothetical protein	A0A2H5BLH4	Streptomyces_phage	9.6e-22	45.1
WP_150509752.1\|1808510_1809137_-	bifunctional DNA primase/polymerase	Q6VY59	Streptomyces_phage	1.0e-40	50.0
WP_150509754.1\|1809883_1810102_-	hypothetical protein	NA	NA	NA	NA
WP_150509755.1\|1810104_1810359_-	hypothetical protein	NA	NA	NA	NA
WP_150509757.1\|1810671_1811046_-	hypothetical protein	Q6VY58	Streptomyces_phage	1.1e-18	46.8

DBSCAN-SWA_3

1850318 : 1858014

Mycobacterium_phage(28.57%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_150515369.1\|1850318_1850741_-	DUF4326 domain-containing protein	A0A2P1CHK0	Mycobacterium_phage	2.3e-17	50.0
WP_150509822.1\|1850938_1851283_-	hypothetical protein	NA	NA	NA	NA
WP_150509823.1\|1851279_1851918_-	hypothetical protein	Q6VY73	Streptomyces_phage	6.3e-06	35.7
WP_150509824.1\|1851914_1853063_-	HNH endonuclease	I6RTT8	Marinomonas_phage	2.4e-11	37.4
WP_150509825.1\|1853062_1853839_-	HNH endonuclease	A0A2K9VH78	Gordonia_phage	2.0e-30	45.9
WP_170316389.1\|1854603_1855404_-	helix-turn-helix domain-containing protein	A0A0R8VCP1	Thermobifida_phage	1.8e-10	30.9
WP_150509828.1\|1855400_1855652_-	hypothetical protein	NA	NA	NA	NA
WP_150509829.1\|1855752_1856124_-	hypothetical protein	NA	NA	NA	NA
WP_150509830.1\|1856196_1857165_-	AAA family ATPase	A0A2H4GSW0	Mycobacterium_phage	8.0e-45	36.9
WP_150509831.1\|1857177_1858014_-	PD-(D/E)XK nuclease-like domain-containing protein	A0A162E1N3	Gordonia_phage	3.7e-38	37.9

DBSCAN-SWA_4

3346976 : 3384383

Streptomyces_phage(86.96%)

coat,holin,capsid,portal,integrase,tail,head

attL 3346703:3346748|attR 3388227:3388272

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
3346703:3346748	attL	NA	NA	NA	NA
WP_150510899.1\|3346976_3348560_-\|integrase	tyrosine-type recombinase/integrase	A0A0U3U8Y8	Bacillus_phage	8.0e-10	21.8
WP_150510900.1\|3348611_3348974_-	hypothetical protein	NA	NA	NA	NA
WP_150510901.1\|3349168_3349603_-	helix-turn-helix domain-containing protein	A0A1V0E635	Streptomyces_phage	1.3e-18	41.1
WP_170316416.1\|3349753_3349996_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_150510903.1\|3349992_3350307_+	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_150510904.1\|3350324_3350582_+	hypothetical protein	NA	NA	NA	NA
WP_150510905.1\|3350578_3351028_+	hypothetical protein	NA	NA	NA	NA
WP_150510906.1\|3351024_3351492_+	hypothetical protein	NA	NA	NA	NA
WP_170316417.1\|3351488_3351656_+	hypothetical protein	NA	NA	NA	NA
WP_150510907.1\|3351652_3351847_+	hypothetical protein	NA	NA	NA	NA
WP_150510908.1\|3351843_3352566_+	hypothetical protein	NA	NA	NA	NA
WP_150510909.1\|3352562_3352841_+	hypothetical protein	NA	NA	NA	NA
WP_150510910.1\|3352931_3353792_+	hypothetical protein	A0A0U4K3K4	Arthrobacter_phage	3.9e-27	34.1
WP_170316418.1\|3353788_3354958_+	AAA family ATPase	NA	NA	NA	NA
WP_150510912.1\|3355605_3355821_+	hypothetical protein	NA	NA	NA	NA
WP_150510913.1\|3355817_3356207_+	hypothetical protein	NA	NA	NA	NA
WP_150510914.1\|3356307_3356799_+	single-stranded DNA-binding protein	A0A2H4JEL4	uncultured_Caudovirales_phage	1.3e-46	64.2
WP_150510915.1\|3356826_3357450_+	hypothetical protein	NA	NA	NA	NA
WP_150510916.1\|3357491_3357734_+	hypothetical protein	NA	NA	NA	NA
WP_170316419.1\|3357830_3357992_+	hypothetical protein	NA	NA	NA	NA
WP_170316420.1\|3358012_3358189_+	hypothetical protein	NA	NA	NA	NA
WP_150510917.1\|3358185_3358914_+	hypothetical protein	NA	NA	NA	NA
WP_150510918.1\|3358913_3359159_+	hypothetical protein	NA	NA	NA	NA
WP_150510919.1\|3359155_3360265_+	hypothetical protein	A0A2D1GNW3	Streptomyces_phage	9.5e-26	35.1
WP_170316421.1\|3360261_3360438_+	hypothetical protein	NA	NA	NA	NA
WP_150510920.1\|3360434_3360764_+	hypothetical protein	NA	NA	NA	NA
WP_150510921.1\|3360765_3360984_+	hypothetical protein	NA	NA	NA	NA
WP_170316422.1\|3361050_3361218_+	hypothetical protein	NA	NA	NA	NA
WP_170316423.1\|3361210_3361375_+	hypothetical protein	NA	NA	NA	NA
WP_150510922.1\|3361462_3363589_+	cell division protein FtsK	NA	NA	NA	NA
WP_150510923.1\|3363791_3364295_+	hypothetical protein	NA	NA	NA	NA
WP_170316424.1\|3364325_3364502_+	hypothetical protein	NA	NA	NA	NA
WP_150510924.1\|3364566_3364836_+	hypothetical protein	NA	NA	NA	NA
WP_150510925.1\|3364859_3365060_+	hypothetical protein	NA	NA	NA	NA
WP_150510926.1\|3365185_3365365_+	hypothetical protein	NA	NA	NA	NA
WP_150515480.1\|3366005_3366431_+	hypothetical protein	D7NW47	Streptomyces_phage	3.3e-19	44.4
WP_150510927.1\|3366414_3368052_+	hypothetical protein	D7NW48	Streptomyces_phage	4.2e-187	61.2
WP_150510928.1\|3368061_3369537_+\|portal	phage portal protein	D7NW49	Streptomyces_phage	1.3e-184	65.5
WP_150510929.1\|3369533_3370478_+	hypothetical protein	A0A2H5BLR1	Streptomyces_phage	8.3e-47	43.1
WP_150510930.1\|3370525_3371275_+	hypothetical protein	D7NW52	Streptomyces_phage	1.5e-35	53.7
WP_150510931.1\|3371290_3372133_+\|coat	P22 coat protein - protein 5 domain protein	D7NW53	Streptomyces_phage	1.8e-69	50.9
WP_150510932.1\|3372148_3372517_+	hypothetical protein	NA	NA	NA	NA
WP_150510933.1\|3372518_3372848_+	hypothetical protein	NA	NA	NA	NA
WP_150510934.1\|3372860_3373457_+	hypothetical protein	D7NW55	Streptomyces_phage	1.2e-46	52.0
WP_150510935.1\|3373453_3373786_+\|head,tail	head-tail adaptor protein	A0A142K636	Streptomyces_phage	1.7e-18	51.9
WP_150510936.1\|3373797_3374124_+	hypothetical protein	D7NW57	Streptomyces_phage	8.1e-26	61.9
WP_150510937.1\|3374123_3374498_+	HK97 gp10 family phage protein	D7NW58	Streptomyces_phage	1.1e-18	45.7
WP_170316425.1\|3374512_3374695_+	hypothetical protein	NA	NA	NA	NA
WP_150510938.1\|3374691_3375093_+	DUF3168 domain-containing protein	D7NW59	Streptomyces_phage	2.2e-41	65.6
WP_150510939.1\|3375105_3375528_+\|capsid	outer capsid protein Hoc	D7NW60	Streptomyces_phage	2.7e-50	68.6
WP_150510940.1\|3375530_3375896_+	hypothetical protein	D7NW62	Streptomyces_phage	6.9e-26	54.2
WP_170316426.1\|3375928_3376240_+	DUF4035 domain-containing protein	D7NW61	Streptomyces_phage	2.7e-10	42.3
WP_150510942.1\|3376282_3378397_+	hypothetical protein	NA	NA	NA	NA
WP_150510943.1\|3378408_3381735_+	hypothetical protein	D7NW64	Streptomyces_phage	1.8e-258	46.5
WP_150510944.1\|3381747_3383361_+	right-handed parallel beta-helix repeat-containing protein	D7NW65	Streptomyces_phage	1.7e-161	55.8
WP_150510945.1\|3383412_3384126_+	N-acetylmuramoyl-L-alanine amidase	A0A0K1Y5X7	Streptomyces_phage	6.4e-84	67.9
WP_150510946.1\|3384128_3384383_+\|holin	holin	A0A0K1Y5A3	Streptomyces_phage	1.5e-22	68.3
3388227:3388272	attR	NA	NA	NA	NA

DBSCAN-SWA_5

3398974 : 3412955

Streptomyces_phage(100.0%)

terminase,capsid,portal,tail

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_150510959.1\|3398974_3399325_+	HNH endonuclease	Q37834	Streptomyces_phage	3.1e-15	38.5
WP_150510960.1\|3399485_3399821_-	hypothetical protein	NA	NA	NA	NA
WP_150510962.1\|3400632_3401112_+\|terminase	P27 family phage terminase small subunit	A0A0K1Y5Q1	Streptomyces_phage	1.4e-50	61.1
WP_150515481.1\|3401092_3402790_+\|terminase	terminase large subunit	A0A2H5BLT3	Streptomyces_phage	1.9e-280	84.2
WP_170316427.1\|3402846_3404271_+\|portal	phage portal protein	A0A2H5BLQ6	Streptomyces_phage	2.5e-172	63.6
WP_150515482.1\|3404384_3405251_+	hypothetical protein	A0A2H5BLR1	Streptomyces_phage	1.9e-98	67.0
WP_150510964.1\|3405259_3405850_+	hypothetical protein	A0A2H5BLQ7	Streptomyces_phage	4.9e-21	53.8
WP_150510965.1\|3405949_3406906_+\|capsid	phage major capsid protein	A0A2H5BLW0	Streptomyces_phage	7.7e-125	72.6
WP_150510966.1\|3407096_3407633_+	hypothetical protein	A0A2H5BLU2	Streptomyces_phage	1.3e-41	57.4
WP_150510967.1\|3407629_3407974_+	hypothetical protein	A0A2P1JSY3	Streptomyces_phage	7.5e-30	57.3
WP_150510968.1\|3407970_3408222_+	hypothetical protein	NA	NA	NA	NA
WP_150510969.1\|3408638_3409196_-	hypothetical protein	NA	NA	NA	NA
WP_150510970.1\|3409260_3409824_+	hypothetical protein	Q6VY45	Streptomyces_phage	6.5e-23	36.7
WP_150510971.1\|3409865_3410177_+	hypothetical protein	NA	NA	NA	NA
WP_150510972.1\|3410564_3412955_+\|tail	phage tail tape measure protein	A0A2H5BLS1	Streptomyces_phage	5.1e-125	57.9

DBSCAN-SWA_6

3416086 : 3427736

Streptomyces_phage(50.0%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_150515485.1\|3416086_3416341_+	hypothetical protein	D7NW67	Streptomyces_phage	2.0e-08	50.0
WP_150510975.1\|3416429_3417224_+	peptidoglycan-binding protein	Q9ZX99	Streptomyces_phage	2.8e-32	72.9
WP_150510976.1\|3417385_3417613_+	hypothetical protein	NA	NA	NA	NA
WP_150515486.1\|3417633_3418191_+	hypothetical protein	A0A2H5BLS8	Streptomyces_phage	1.3e-39	47.3
WP_150510977.1\|3418326_3419163_+	hypothetical protein	K4HZ42	Streptomyces_virus	4.0e-85	57.9
WP_150510978.1\|3419240_3419939_+	hypothetical protein	K4I334	Streptomyces_virus	7.0e-59	50.4
WP_150510979.1\|3419959_3420505_+	DNA cytosine methyltransferase	Q858Z2	Streptomyces_virus	2.7e-50	60.9
WP_150510980.1\|3420566_3421049_+	DNA (cytosine-5-)-methyltransferase	A0A1D8ETM2	Propionibacterium_phage	2.0e-17	54.3
WP_150510981.1\|3422086_3424522_+	toprim domain-containing protein	A0A2H5BLZ0	Streptomyces_phage	0.0e+00	66.3
WP_150510982.1\|3424591_3426445_+	DNA polymerase	K4HYK3	Streptomyces_virus	2.0e-238	67.8
WP_150510983.1\|3426923_3427736_+	sigma-70 family RNA polymerase sigma factor	A0A2H5BLU6	Streptomyces_phage	7.4e-20	28.0

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_CP023690

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CRISPR-Cas detection and classification

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Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection