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_CP023564	Brachybacterium ginsengisoli strain DCY80 chromosome, complete genome	4 crisprs	csa3,cas3,DEDDh,Cas9_archaeal,WYL,DinG	1	3	0	0

Cas Category Instructions

Results visualization

1. NZ_CP023564

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP023564_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023564_1

126136-126246

Orphan

Consensus_repeat	Method
CGACCACGAGGGCCACGACCACGA	CRISPRCasFinder

2 spacers

The CRISPR arrays of NZ_CP023564_1

>merge|NZ_CP023564|1|126136-126246|CRISPRCasFinder
CGGCGGCGAGGGGGATGACCACGAGGATCACGACCACGAGGGCCACGACCACGAGGGCACTGCGGACGAGGCGTCGGACGCCGGCGGCGACCACGAGGGCCACGACCACTG

>NZ_CP023564|1|1|126136-126246|CRISPRCasFinder
CGGCGGCGAGGGGGATGACCACGA	GGATCACGACCACGAGGGCCA
CGACCACGAGGGCACTGCGGACGA	GGCGTCGGACGCCGGCGG
CGACCACGAGGGCCACGACCACTG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023564.1\|WP_096800870.1\|131110_131482_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|379228
NZ_CP023564.1\|WP_096797924.1\|128456_129377_+\|sulfite-exporter-TauE/SafE-family-protein	unknown	unknown	gnl\|CDD\|376667
NZ_CP023564.1\|WP_096797927.1\|132889_133798_+\|formate/nitrite-transporter-family-protein	unknown	unknown	gnl\|CDD\|376497
NZ_CP023564.1\|WP_096797919.1\|120469_122866_+\|beta-N-acetylglucosaminidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|369423
NZ_CP023564.1\|WP_096797914.1\|116299_117694_+\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|270451
NZ_CP023564.1\|WP_096797929.1\|134658_135567_+\|alpha/beta-hydrolase	unknown	unknown	gnl\|CDD\|366166
NZ_CP023564.1\|WP_096797917.1\|119711_120104_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096797918.1\|120115_120331_+\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224393
NZ_CP023564.1\|WP_096797915.1\|117851_118610_+\|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl\|CDD\|176524
NZ_CP023564.1\|WP_096797928.1\|133864_134662_+\|IclR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224332
NZ_CP023564.1\|WP_096797920.1\|123105_124449_+\|NADP-specific-glutamate-dehydrogenase	unknown	unknown	gnl\|CDD\|181834
NZ_CP023564.1\|WP_096797922.1\|126286_127075_-\|fructosamine-kinase-family-protein	unknown	unknown	gnl\|CDD\|225547
NZ_CP023564.1\|WP_096797923.1\|127170_128304_-\|aminoglycoside-phosphotransferase-family-protein	unknown	unknown	gnl\|CDD\|366736
NZ_CP023564.1\|WP_096797916.1\|118793_119534_+\|glycerophosphodiester-phosphodiesterase	unknown	unknown	gnl\|CDD\|176524
NZ_CP023564.1\|WP_096797926.1\|131769_132765_-\|formimidoylglutamase	unknown	unknown	gnl\|CDD\|237499
NZ_CP023564.1\|WP_096800869.1\|115283_116081_+\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP023564.1\|WP_096797930.1\|135686_136226_+\|MOSC-domain-containing-protein	unknown	unknown	gnl\|CDD\|225167
NZ_CP023564.1\|WP_096797913.1\|114138_115179_+\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224096
NZ_CP023564.1\|WP_096797925.1\|129872_130412_+\|DinB-family-protein	unknown	unknown	gnl\|CDD\|368218
NZ_CP023564.1\|WP_096797912.1\|112510_113593_-\|LacI-family-DNA-binding-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224525

Protein	Function_ID	Function_description	E-value
NZ_CP023564.1\|WP_096800870.1\|131110_131482_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|379228	pfam13508, Acetyltransf_7, Acetyltransferase (GNAT) domain. This domain catalyzes N-acetyltransferase reactions.	1.44455e-12
NZ_CP023564.1\|WP_096797924.1\|128456_129377_+\|sulfite-exporter-TauE/SafE-family-protein	gnl\|CDD\|376667	pfam01925, TauE, Sulfite exporter TauE/SafE. This is a family of integral membrane proteins where the alignment appears to contain two duplicated modules of three transmembrane helices. The proteins are involved in the transport of anions across the cytoplasmic membrane during taurine metabolism as an exporter of sulfoacetate. This family used to be known as DUF81.	9.73467e-26
NZ_CP023564.1\|WP_096797927.1\|132889_133798_+\|formate/nitrite-transporter-family-protein	gnl\|CDD\|376497	pfam01226, Form_Nir_trans, Formate/nitrite transporter.	1.76459e-33
NZ_CP023564.1\|WP_096797919.1\|120469_122866_+\|beta-N-acetylglucosaminidase-domain-containing-protein	gnl\|CDD\|369423	pfam07555, NAGidase, beta-N-acetylglucosaminidase. This family has previously been described as a hyaluronidase. However, more recently it has been shown that this family has beta-N-acetylglucosaminidase activity.	8.13108e-143
NZ_CP023564.1\|WP_096797914.1\|116299_117694_+\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|270451	cd14748, PBP2_UgpB, The periplasmic-binding component of ABC transport system specific for sn-glycerol-3-phosphate; possesses type 2 periplasmic binding fold. This group includes the periplasmic component of an ABC transport system specific for sn-glycerol-3-phosphate (G3P) and closely related proteins from archaea and bacteria. Under phophate starvation conditions, Escherichia coli can utilize G3P as phosphate source when exclusively imported by an ATP-binding cassette (ABC) transporter composed of the periplasmic binding protein, UgpB, the transmembrane subunits, UgpA and UgpE, and a homodimer of the nucleotide binding subunit, UgpC. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 proteins are 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. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. 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.	6.32285e-75
NZ_CP023564.1\|WP_096797929.1\|134658_135567_+\|alpha/beta-hydrolase	gnl\|CDD\|366166	pfam00561, Abhydrolase_1, alpha/beta hydrolase fold. This catalytic domain is found in a very wide range of enzymes.	5.13828e-23
NZ_CP023564.1\|WP_096797930.1\|135686_136226_+\|MOSC-domain-containing-protein	gnl\|CDD\|225167	COG2258, COG2258, Uncharacterized protein conserved in bacteria [Function unknown].	1.14326e-27
NZ_CP023564.1\|WP_096797918.1\|120115_120331_+\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|224393	COG1476, COG1476, Predicted transcriptional regulators [Transcription].	3.10657e-27
NZ_CP023564.1\|WP_096797915.1\|117851_118610_+\|glycerophosphodiester-phosphodiesterase	gnl\|CDD\|176524	cd08582, GDPD_like_2, Glycerophosphodiester phosphodiesterase domain of uncharacterized bacterial glycerophosphodiester phosphodiesterases. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in a group of uncharacterized bacterial glycerophosphodiester phosphodiesterase and similar proteins. They show high sequence similarity to Escherichia coli glycerophosphodiester phosphodiesterase, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols.	1.79914e-43
NZ_CP023564.1\|WP_096797928.1\|133864_134662_+\|IclR-family-transcriptional-regulator	gnl\|CDD\|224332	COG1414, IclR, Transcriptional regulator [Transcription].	5.83444e-50
NZ_CP023564.1\|WP_096797920.1\|123105_124449_+\|NADP-specific-glutamate-dehydrogenase	gnl\|CDD\|181834	PRK09414, PRK09414, NADP-specific glutamate dehydrogenase.	0
NZ_CP023564.1\|WP_096797922.1\|126286_127075_-\|fructosamine-kinase-family-protein	gnl\|CDD\|225547	COG3001, COG3001, Uncharacterized protein conserved in bacteria [Function unknown].	3.97814e-41
NZ_CP023564.1\|WP_096797923.1\|127170_128304_-\|aminoglycoside-phosphotransferase-family-protein	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.	1.66922e-14
NZ_CP023564.1\|WP_096797916.1\|118793_119534_+\|glycerophosphodiester-phosphodiesterase	gnl\|CDD\|176524	cd08582, GDPD_like_2, Glycerophosphodiester phosphodiesterase domain of uncharacterized bacterial glycerophosphodiester phosphodiesterases. This subfamily corresponds to the glycerophosphodiester phosphodiesterase domain (GDPD) present in a group of uncharacterized bacterial glycerophosphodiester phosphodiesterase and similar proteins. They show high sequence similarity to Escherichia coli glycerophosphodiester phosphodiesterase, which catalyzes the degradation of glycerophosphodiesters to produce sn-glycerol-3-phosphate (G3P) and the corresponding alcohols.	3.63899e-51
NZ_CP023564.1\|WP_096797926.1\|131769_132765_-\|formimidoylglutamase	gnl\|CDD\|237499	PRK13773, PRK13773, formimidoylglutamase; Provisional.	1.76724e-134
NZ_CP023564.1\|WP_096800869.1\|115283_116081_+\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	8.37598e-75
NZ_CP023564.1\|WP_096797913.1\|114138_115179_+\|sugar-ABC-transporter-permease	gnl\|CDD\|224096	COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].	1.66937e-90
NZ_CP023564.1\|WP_096797925.1\|129872_130412_+\|DinB-family-protein	gnl\|CDD\|368218	pfam04978, DUF664, Protein of unknown function (DUF664). This family is commonly found in Streptomyces coelicolor and is of unknown function. These proteins contain several conserved histidines at their N-terminus that may form a metal binding site.	4.16956e-38
NZ_CP023564.1\|WP_096797912.1\|112510_113593_-\|LacI-family-DNA-binding-transcriptional-regulator	gnl\|CDD\|224525	COG1609, PurR, Transcriptional regulators [Transcription].	1.8967e-54

>NZ_CP023564.1|WP_096797920.1|123105_124449_+|NADP-specific-glutamate-dehydrogenase
MLDSTLQATYDQVLRRNAGEPEFHQAVREVFESLEVIQDRHPEYQDHGILMRLCEPERQIIFRVPWVDDDGIVQVNRGFRVEYNSALGPYKGGLRFHPSVNLGIVKFLGFEQIFKNSLTGLPIGGGKGGSDFDPHGRSDGEVMRFCQSFMTELHRHMGEYTDVPAGDIGVGAREIGYLFGQYKRLTNRYEAGVLTGKGLDWGGSLVRKEATGYGAAIFADEMLKARGSSVDGRRVAVSGSGNVALYAIEKVRQLGGIAVTASDSSGYVVDENGIDLELLQQIKEVERGRITEYAERRGNGARFVKGGSVWDVPVDIAVPSATQNELDADAARTLVKNGVKAVSEGANMPCTPDAVAVLREAGVAFGPGKAANAGGVATSALEMQQNASRDAWSFEHTENRLTEIMKNIHTTCLETAEEVGRPGDYAVGANVAGFRKVADAMIAFGVI
>NZ_CP023564.1|WP_096797919.1|120469_122866_+|beta-N-acetylglucosaminidase-domain-containing-protein
MHRSTSSSSAPSALTRRAALGLGLAAGGALALPGTSALADGGTPGRVPEMRPAPQAVGTAAGEVVLGGSVTVHVGEETDAVARAALTALLESVGCTVSVQVGGEVRPGGTRVHLGTPEDNPTLADALEVVGVQGPEDLAADGYVLAAARHRGATLVLAGHDARGTFYAVQTLRQLLAGSTRVPAVQVRDEPLMEIRGAIEGFYGIPWSHRSRLDHFVFYGEHKLNTYIYTPKDDLLLRSKWRELYEGDQLADLAELVETANANHVSFTFALSPGNDITYGSDEDFEATVTKFEQLRELGVTSFYIALDDIPTELGEEDAAQFGSLAEAQVHYLNRLQTDYVEAHGLAPLQTVPTHYSGSEPTAYKADFGSGAHPDIRIQWTGEGVFSPTITEESVRTAVASYRTEHLYIWDNFPVNDGRRDRLFLNPLEGRAPTLHEHLAGFTANPMIQPYASLISLANYADYCWNPPVYEAESSWEAAVDELAGTEPAIREALRVFTDLNQHWPYRAGSPAAPALSADVEAFWAAYADGRAEGGELAARLEAIVGLEDSLAPMASEGFYADTRAWMVAAGHWSRALQAQLEMLRAIAEDRLEDASAAAAEVAPHLEAAGEATVPDQRADGVYTENQIVPSVGDGVFDAFLARAWEELRAVRPTDLSLPFRGLPAAATTTLGTYRDYEIGRIVDGDPASMFWSSSAPTVGDVVQVELEENHPVRYVQVQMAKSDATPGDQIYQGVLELSADGETWTEIGATDGTAVARARLDEPVDARFCRLRVTAKNPGGQWVQIREFGVGEVPPGS
>NZ_CP023564.1|WP_096797918.1|120115_120331_+|helix-turn-helix-transcriptional-regulator
MRNDLKARRAERRWSQAELGTALGVSRQTVIALENDRYDPSLPLAFRIAALFGCSIEEIFQPEADGADGAA
>NZ_CP023564.1|WP_096797917.1|119711_120104_+|hypothetical-protein
MTAATTPRSRVNRVFAVRFVGGVVLYVASLALTQVAQAVGVPAWLPALLVLPAVGLMAWANIDMYRSGDEFERRKIAEAVMVAFVVSVPLILAVGVLQFSLLPAMNWIFAFSILMLAWIAGTIVSAVRYR
>NZ_CP023564.1|WP_096797916.1|118793_119534_+|glycerophosphodiester-phosphodiesterase
MTNQSSPAPQQRPAIVGHRGASAHAPENTLAAFRRALEDGAQLLECDVHLSADGEVVVMHDETIDRTVASDSPLRTGAIGELTRAQLDTVLLEGGERVPSLAELLEMTTAPVFIEVKVAAAAQAVAEILTALPKGSPAAASTVISFHVDALAEIRRTTETPVSYLVGQVDEQAIATARELGAAGIGPSIKGLSLQAAEAVHEAGLAVNPWTVNTVPQLEVALACGVDTITTDDPAWVQCELDVRLG
>NZ_CP023564.1|WP_096797915.1|117851_118610_+|glycerophosphodiester-phosphodiesterase
MTFQQPEIVGHRGAAALSPENTVQSFRRGVAEGSTWLECDVHLSSDGQDVIIHDATLDRTAQADSPLRTGAVSDLTRTQLDRVLVGEGQHIPTLAQVLEVAVREDGNRIPVLVEIKAVDAAERVVAILQDYFVPTAWQEPDGAPAWVISFHEEPLRRTRELAPQIPLMLTTTATSPQWWEACRDLGVAQAGVRIADARQADVERAKELGVALNLWTARSEEELERALELGCDTITVDDPAWAAVEIERRTGV
>NZ_CP023564.1|WP_096797914.1|116299_117694_+|ABC-transporter-substrate-binding-protein
MSRTPFNVSRRSMLAALGLGTGAAGLAACGAPGGGGGGEDGTVRDGFSQADLTVPKEYEGRTPILFWAPFTDTNYEVLSKQFAEFNESQDEIVAIAESVGGYVDLNQKFTAALQARTVPDIVCFPEMQWLQFHQSGALAPLDGYFDDEWNLDKYIQNYVAEGKAGGDTYVVPFARSTPLFYYNKTRYIEAGLPEEGPETWEDLAEFAPELAKIQVDGRPLSAITLAADAWGGQADIWGFGGANSDQDFAVSINDERGVEWLEWMRKFVHDDGYGYLAQDSATDFASGLAAGWRGSTASLTGQTQATEGVFEIGTAFMLSKEGEEKQVPTGGSGLSIVKTDSQDRQDACAELFRFLGQPEKSAEWHVGTGYVPIVEAARDTQVVKDLVAKNPNYGVSLAQLENARTADYTNWDQGSITEIGAAMGQVFGDGADPQKVLDTLAATLQETLDDNREDYEAVAFEGWN
>NZ_CP023564.1|WP_096800869.1|115283_116081_+|carbohydrate-ABC-transporter-permease
MLIAGVVATIVVFTLPLYWLFSSALKPHQDIYTWPLQWIPGELTLANFTQAWNSAPFDRFFVNSIITTGVGTFLEITLAILCAYAFVFVEFRFKKIAFALIIASMMLPGHVTLIVNYITIANLGWLNSYAGIILPGIASAFAMFLLYQYMRTIDKDILQAAEIDGAGHLRRMLTIVVPLSSPMILTATLIVMVGKWNEYVWPLIVTSTADMRTLPIGLLFLRSQEGYSNWGVIMAGAVFVSLPMLILFFLAQKRIIGGLAAGAMK
>NZ_CP023564.1|WP_096797913.1|114138_115179_+|sugar-ABC-transporter-permease
MSISVRSPRTDPAVPSGAAQAEAPVGPSGDSSRGATATGPRGRSEERRRSPQRRRRARRDALLFGLLIAPNLLAIIVFSYYPALYNIGLSFFDWDFVAPSPDFVGLENYTDLFTNPNFGQVMLNTLIFTGVSVVGSLALGLVLGSLLATKVPLTGFAQTMAFAPHMLPGAAVGILWLFMFDPNYGLSRWAFSLFGADSPAWTTTSDWSLWAITIAYTWQRLGFVTVICYTAILDLPKDLYEAAALDGAHGWKLFRHLTLPLLSPITFFLSITGIISAAQAFDIISIMTNGGPGISSSTLSWMVYEEAFQKFDIGKASAGATVLLVLLLAITYVQVRYGEKKVNYDS
>NZ_CP023564.1|WP_096797912.1|112510_113593_-|LacI-family-DNA-binding-transcriptional-regulator
MARPPTMEDVARAAGVSRSTVSRVFQNGGERVSPDAMIRIHEAAKRLGYVHNLVASGLAMRQGRQLGLLIRDATNPAYGHLHTELNRAVEAGGRTLISVTASRHDYGTAEVEGLNRLIGQRVAGVFVGTGVTAAEDLVETVTATPMMIVGRPNEHPQIESVSYDERAHGRLMAEEIAAAGHRRIAVLTAPLLYSRVFDLRMRSLVDRYHELGLATVPVDLLPVEQGVVRALDLAAEQALTCIVCPVDYVALDLLRAAAARGVRVPEEVSTVGFDGMGDGLDLIGLATIRLPVEEVARSAVARMEELLADAREEPADPSAPPDSAGPSAAADRRPAVRHTAIPGRLLPGRTLGPAPERPRS
>NZ_CP023564.1|WP_096797922.1|126286_127075_-|fructosamine-kinase-family-protein
MSDFVKNADNAPGGYVAAEAAGLRWLAEPQVVPVVEVIAEEKKELRLARLESVEPTAGAARELGRGLARLHDAGAPSFGWTPADDAFFGPLESPFAVTAAPSTDFAGYWADDRLRPLADTVTRTLGADGHDTVDEAIDIIADGAFDGVSGEGEEEPARVHGDLWSGNVLWTADGATLIDPAAHGGHRLEDLAMLSLFGAPFLDEILEGYEAEHPLPEGWEQDLPAHQLFGLLGHVRVFGEAYVDQTIATARAIITRADELGF
>NZ_CP023564.1|WP_096797923.1|127170_128304_-|aminoglycoside-phosphotransferase-family-protein
MAPHRPEQAPAPLDPASPAMGELLRRSWRAGTLMLPSAPAPSPRTPSAPTAAQSGSLQVALAGVGERFAAWRVIPPGGAALIVRIPHVAPDELHQDLAHEIAALSLLPSGVGPDPVAVHDDPATSPLGRPFVVTTAIPGEVAAPTAWSAAHLRAHAAHLARLHAVSAPGRGPVSTGPDPWSAIAPGPQHLLPEVEGELRAAQVAHGAAIAEHRLAPLLEAALEVVAATEAQFAQLDGFVLCHGDLCATNILWDGADPAGGPPAVQYIDFEWAQGDDPARDLAILGGSVHGGPWYVPLTDEQVSAFVDAYVRARGELGEVPDSVADTASLRDRMRAWTAYERSAMLVHVASRAATSAAHRRVLPALRGTLAVTLGVDV
>NZ_CP023564.1|WP_096797924.1|128456_129377_+|sulfite-exporter-TauE/SafE-family-protein
MELVLLAIGVGLCVGVVVGALGAGGGILAVPVLVFGLGMPAHSATASSLIIVLITALASLPHHARNRNVDWRNGLVFAGVSVVGAVLGSRLSALVPEHLLLTLFGAMLVAVAIAMLRRALRTRREERAEAAAHGRAVDADCAETVATHDDPVLDQPGPDTVEAADGMLRHHGEPELPTTPARPSSPRLPLVIAAATLTGFLTGFFGVGGGFIVVPMLVIALGLAMRRASGTSLLVMIIATITSLLARLGTDVQIDWVTTLVFAAGSAVGGILGGPLSSKARPSTLALLFSVLLGGVAAVTLVQTLL
>NZ_CP023564.1|WP_096797925.1|129872_130412_+|DinB-family-protein
MTSPDPRSSARPDTRVEPSMMAGERESLDGWLEYYRETVLLKIDGLDGEQLARRSVPPSALSPAGILRHLADVEAYWLLEVLHGEEQPDPHCSDDNPDGDFLDATAETALADVAAYREQVEASRAAQARWPDLDAPVLGWRRGQELNLRWILSHLLEEYARHQGHLDLLCEAVDGRTGE
>NZ_CP023564.1|WP_096800870.1|131110_131482_+|GNAT-family-N-acetyltransferase
MLELYSAVGWSAYTEDPATLERSVLGSEHVVTARRDGELLGMARVVGDGATLAYLQDVLVRPDAHRTGIGRSLVEAAFAPFAAVRQKVLLTDAEPSQRAFYESLGFVEAHDHDPGLRAFVRLR
>NZ_CP023564.1|WP_096797926.1|131769_132765_-|formimidoylglutamase
MTTSPEAGTPWTGRYDGDGPEHARWHQRVLQGAVGAAPDPAADHVALLGFRSDEGVRRNRGRVGAADGPDALRRALAPMALHGPLARGEVALHDLGDAVTEGEDLEGGQAAAAALTSAALDRAGAQLSVVLGGGHETAWSSYQGLMGSGLGPRARQRWGVLNLDAHFDLREEPRPTSGTPFAQMAAAEQRAGRDLHYAVLGIAEPSNTGALFDRARDLGVRWWTDEQCLEAGAEGITRFVEEFTAELDLLYLTIDLDVLPAATAPGVSAPAAYGVPLPLIAAAVRAAAASGKLTLLDVVELNPSLDVDGRTARAAARLIDDAVRLVTGSEP
>NZ_CP023564.1|WP_096797927.1|132889_133798_+|formate/nitrite-transporter-family-protein
MDQHDQHDQHDQHDQHRRHDQAAERRQLGSSDQPVEDVLVQEFESTVAEGANRLNRTWRALIITGLFGGIDVGLGLLAMLAVLDATGSKLLGGLAFGIGLYALRLAHSELFTEDFLVPINAIVAGHGTWGQLLRLWVTTLVTNLVGGWSFTWVVVAAFPRFDDVLMESTSSYMDKGLTLETAALAVLAGFTITLVTRMNQGSKEGIATLANSLISGLLVVGLGMLHGALSSAVIFGAMHAGAETTYLQWLVWFAWVIPLNMAGGLVMLTLPRLVRTWELATKERAAQRGRGRMSASDEPAAG
>NZ_CP023564.1|WP_096797928.1|133864_134662_+|IclR-family-transcriptional-regulator
MTTPKVPAADATLRLLTLLASRRSPVPAARLAEELGLPRSRTYDLLTTLVEHGYVLHLDQERLYGLGPAAHELSGAYLRQEPLARIGRRVIEAMVDEVGESGHLAVLHGRDVLYVIEERARNRPSLVSDVGVRIPSHLTASGRAILAELPPAQLRALYGHAADFTARTEATGPSRPKELRELLVRVRAEGIAREQGEVTEELASVAAVVRDHAGWPAAAVALTFVERDADEERRERCAEAVRRAADEITRRLRGRPTDERTGERR
>NZ_CP023564.1|WP_096797929.1|134658_135567_+|alpha/beta-hydrolase
MTEQESREFVTMSDGARLATVTVPGPAGAPAVIIVHGGPGLWDHLEALGDLLDGRATVHRYDQRRCGRSTGPDGRPAIEDPQGPTPADLTIERSVADIEELRRAFGHEHVVLVGHSFGATLALAYAGTHPERVSALAYVDGVGIGDWRTPYRAERARRMAPWAESLAALDGRERTRDEETEWRRLQWTSDYADPSAGYDLALEMACSPHAINHQANRALGAAGAIADIDQITWITAVRCPVTVVHGTEDPRPVRPVLALAAHARAPRKRAVAGAGHLPWVEQPEQLREILAELVLSAGHRFG
>NZ_CP023564.1|WP_096797930.1|135686_136226_+|MOSC-domain-containing-protein
MNPTVVSVHVSAEHGFSKPRADSIELLEGIGVRGDAHAGVTVKHRSRVARNPDQPNLRQVHLIHQELFAHLAEQGHEVAPGELGENITTAGVDLLALPVGTRLRIGEAVVVVTGLRNPCQQIEDFRPGLLRSVLPRDDAGTVHRLTGVMGIVARGGTVRATDEISVDLPPEPHHPLTQV

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Crispr_ID: NZ_CP023564_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023564_2

592107-593204

Orphan

Consensus_repeat	Method
NAACACNGACGTGAACAC	CRT

20 spacers

The CRISPR arrays of NZ_CP023564_2

>merge|NZ_CP023564|2|592107-593204|CRT
CAACACGGACGTGAACACCGAGGTCAACACCGCTGAGAACACGGACGTCAACACGGATGTGAACACGGCGGACAACGCTGCTGAGAACACCGACGTCAACACCGATGTGAACACGGCAGATAACGCTGCTGAGAACACGGATGTCAACACGGATGTCAACACGGCGGACAACGCTGCCGAGAACACTGACGTGAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACGGACGTGAACACGGCAGATAACGCTGCCGAGAACACTGACGTGAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACGGACGTGAACACGGCGGACAATGCTGCCGAGAACACCGACGTGAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACGGACGTGAACACGGCGGACAACGCTGCCGAGAACACGGATGTCAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACCGACGTGAACACGGCAGACAACGCTGCCGAGAACACCGACGTGAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACCGACGTGAACACGGCAGACAATGCTGCCGAGAACACCGACGTGAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACCGACGTGAACACGGCAGACAATGCTGCCGAGAACACCGACGTGAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACCGACGTGAACACGGCAGACAATGCTGCCGAGAACACCGACGTGAACACCGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGTCAACACCGACGTGAACACGGCAGACAATGCTGCCGAGAACACCGACGTCAACACCGAGGTCAACACCGCTGAGAACACAGGTGACAACAC

>NZ_CP023564|2|1|592107-593204|CRT
CAACACGGACGTGAACAC	CGAGGTCAACACCGCTGAGAACACGGACGT
CAACACGGATGTGAACAC	GGCGGACAACGCTGCTGAGAACACCGACGT
CAACACCGATGTGAACAC	GGCAGATAACGCTGCTGAGAACACGGATGTCAACACGGATGTCAACACGGCGGACAACGCTGCCGA
GAACACTGACGTGAACAC	CGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACGGACGTGAACAC	GGCAGATAACGCTGCCGA
GAACACTGACGTGAACAC	CGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACGGACGTGAACAC	GGCGGACAATGCTGCCGA
GAACACCGACGTGAACAC	CGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACGGACGTGAACAC	GGCGGACAACGCTGCCGAGAACACGGATGT
CAACACCGAGGTGAACAC	TGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACCGACGTGAACAC	GGCAGACAACGCTGCCGA
GAACACCGACGTGAACAC	CGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACCGACGTGAACAC	GGCAGACAATGCTGCCGA
GAACACCGACGTGAACAC	CGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACCGACGTGAACAC	GGCAGACAATGCTGCCGA
GAACACCGACGTGAACAC	CGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACCGACGTGAACAC	GGCAGACAATGCTGCCGA
GAACACCGACGTGAACAC	CGAGGTGAACACTGCTGACAACACTGAGGTGAACGCGGCGGACAACACCGAGGT
CAACACCGACGTGAACAC	GGCAGACAATGCTGCCGA
GAACACCGACGTCAACAC	CGAGGTCAACACCGCTGA
GAACACAGGTGACAACAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023564.1\|WP_096798254.1\|583662_584040_+\|response-regulator	unknown	unknown	gnl\|CDD\|381116
NZ_CP023564.1\|WP_151904648.1\|588397_588934_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096798262.1\|596467_597895_-\|PepSY-domain-containing-protein	unknown	unknown	gnl\|CDD\|377164
NZ_CP023564.1\|WP_096798269.1\|604987_606874_+\|glycoside-hydrolase-family-127-protein	unknown	unknown	gnl\|CDD\|369609
NZ_CP023564.1\|WP_096798251.1\|578893_580588_-\|heparinase-II/III-family-protein	unknown	unknown	gnl\|CDD\|377945
NZ_CP023564.1\|WP_096798268.1\|603191_604991_+\|glycoside-hydrolase-family-2	unknown	unknown	gnl\|CDD\|225789
NZ_CP023564.1\|WP_096798255.1\|584020_585910_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|133058
NZ_CP023564.1\|WP_096798266.1\|600540_601158_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_151904647.1\|586046_587744_-\|PAS-domain-containing-protein	unknown	unknown	gnl\|CDD\|223715
NZ_CP023564.1\|WP_151904646.1\|582292_583342_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096798261.1\|595305_596397_+\|HTTM-domain-containing-protein	unknown	unknown	gnl\|CDD\|214802
NZ_CP023564.1\|WP_096798260.1\|594556_595309_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096798259.1\|589080_589266_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096798265.1\|599878_600490_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096798263.1\|597902_598700_-\|class-F-sortase	unknown	unknown	gnl\|CDD\|320678
NZ_CP023564.1\|WP_096798257.1\|587822_588275_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_169928776.1\|580584_582177_-\|glycosyltransferase	unknown	unknown	gnl\|CDD\|274954
NZ_CP023564.1\|WP_096798250.1\|577426_578680_-\|UDP-N-acetyl-D-mannosamine-dehydrogenase	unknown	unknown	gnl\|CDD\|182940
NZ_CP023564.1\|WP_096798264.1\|598701_599475_-\|CHRD-domain-containing-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096798267.1\|602515_603043_+\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP023564.1\|WP_096798261.1\|595305_596397_+\|HTTM-domain-containing-protein	gnl\|CDD\|214802	smart00752, HTTM, Horizontally Transferred TransMembrane Domain. Sequence analysis of vitamin K dependent gamma-carboxylases (VKGC) revealed the presence of a novel domain, HTTM (Horizontally Transferred TransMembrane) in its N-terminus. In contrast to most known domains, HTTM contains four transmembrane regions. Its occurrence in eukaryotes, bacteria and archaea is more likely caused by horizontal gene transfer than by early invention. The conservation of VKGC catalytic sites indicates an enzymatic function also for the other family members.	1.03499e-47
NZ_CP023564.1\|WP_096798262.1\|596467_597895_-\|PepSY-domain-containing-protein	gnl\|CDD\|377164	pfam03929, PepSY_TM, PepSY-associated TM region. The PepSY_TM family is so named because it is an alignment of up to five transmembranes helices found in bacterial species some of which carry a nested PepSY domain, pfam03413.	4.55568e-63
NZ_CP023564.1\|WP_096798269.1\|604987_606874_+\|glycoside-hydrolase-family-127-protein	gnl\|CDD\|369609	pfam07944, Glyco_hydro_127, Beta-L-arabinofuranosidase, GH127. One member of this family, from Bidobacterium longicum, UniProtKB:E8MGH8, has been characterized as an unusual beta-L-arabinofuranosidase enzyme, EC:3.2.1.185. It rleases l-arabinose from the l-arabinofuranose (Araf)-beta1,2-Araf disaccharide and also transglycosylates 1-alkanols with retention of the anomeric configuration. Terminal beta-l-arabinofuranosyl residues have been found in arabinogalactan proteins from a mumber of different plantt species. beta-l-Arabinofuranosyl linkages with 1-4 arabinofuranosides are also found in the sugar chains of extensin and solanaceous lectins, hydroxyproline (Hyp)2-rich glycoproteins that are widely observed in plant cell wall fractions. The critical residue for catalytic activity is Glu-338, in a ET/SCAS sequence context.	1.10679e-28
NZ_CP023564.1\|WP_096798254.1\|583662_584040_+\|response-regulator	gnl\|CDD\|381116	cd17574, REC_OmpR, phosphoacceptor receiver (REC) domain of OmpR family response regulators. OmpR-like proteins are one of the most widespread transcriptional regulators. OmpR family members contain REC and winged helix-turn-helix (wHTH) DNA-binding output effector domain. They are involved in the control of environmental stress tolerance (such as the oxidative, osmotic and acid stress response), motility, virulence, outer membrane biogenesis and other processes. REC domains function as phosphorylation-mediated switches within response regulators, but some also transfer phosphoryl groups in multistep phosphorelays.	1.70435e-33
NZ_CP023564.1\|WP_096798263.1\|597902_598700_-\|class-F-sortase	gnl\|CDD\|320678	cd05829, Sortase_F, Sortase domain found in the class F family of sortases. Class F sortases are mainly present in Actinobacteria, Chlorobacteria and Firmicutes. Their functions are largely unknown.	1.20651e-49
NZ_CP023564.1\|WP_096798251.1\|578893_580588_-\|heparinase-II/III-family-protein	gnl\|CDD\|377945	pfam07940, Hepar_II_III, Heparinase II/III-like protein. This family features sequences that are similar to a region of the Flavobacterium heparinum proteins heparinase II and heparinase III. The former is known to degrade heparin and heparin sulphate, whereas the latter predominantly degrades heparin sulphate. Both are secreted into the periplasmic space upon induction with heparin.	1.33323e-11
NZ_CP023564.1\|WP_096798268.1\|603191_604991_+\|glycoside-hydrolase-family-2	gnl\|CDD\|225789	COG3250, LacZ, Beta-galactosidase/beta-glucuronidase [Carbohydrate transport and metabolism].	3.55226e-34
NZ_CP023564.1\|WP_096798255.1\|584020_585910_-\|glycosyltransferase	gnl\|CDD\|133058	cd06436, GlcNAc-1-P_transferase, N-acetyl-glucosamine transferase is involved in the synthesis of Poly-beta-1,6-N-acetyl-D-glucosamine. N-acetyl-glucosamine transferase is responsible for the synthesis of bacteria Poly-beta-1,6-N-acetyl-D-glucosamine (PGA). Poly-beta-1,6-N-acetyl-D-glucosamine is a homopolymer that serves as an adhesion for the maintenance of biofilm structural stability in diverse eubacteria. N-acetyl-glucosamine transferase is the product of gene pgaC. Genetic analysis indicated that all four genes of the pgaABCD locus were required for the PGA production, pgaC being a glycosyltransferase.	7.46851e-63
NZ_CP023564.1\|WP_096798250.1\|577426_578680_-\|UDP-N-acetyl-D-mannosamine-dehydrogenase	gnl\|CDD\|182940	PRK11064, wecC, UDP-N-acetyl-D-mannosamine dehydrogenase; Provisional.	0
NZ_CP023564.1\|WP_151904647.1\|586046_587744_-\|PAS-domain-containing-protein	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	2.69953e-46
NZ_CP023564.1\|WP_169928776.1\|580584_582177_-\|glycosyltransferase	gnl\|CDD\|274954	TIGR04063, Glycosyl_transferase_group_1, PEP-CTERM/exosortase A-associated glycosyltransferase, Daro_2409 family. PEP-CTERM/exosortase is a protein-sorting system associated with exopolysaccharide production. Members of this protein family are group 1 glycosyltransferases (see pfam00534) in which the overwhelming majority occur in species with the EpsH1 form of exosortase (see TIGR03109), and usually co-clustered with the exosortase. A typical member is Daro_2409 from Dechloromonas aromatica RCB.	4.68048e-96

>NZ_CP023564.1|WP_096798259.1|589080_589266_+|hypothetical-protein
MSGSGAVSSRGRRISALLAGGLAPGAGAAVTLAAFADPAVEAGAANPTHVVSRATAVEDCF
>NZ_CP023564.1|WP_151904648.1|588397_588934_+|hypothetical-protein
MRDTLRRRAPQRRWSVRLRVLLAAGLVLGAGATSSLADWWDTEQASATFRAGEVPAPALTRACEYSPGVIGLGARVRIFWALPPGYSLADVRVLASTSGLGSVLAPLTGFSVQGNTQQLADGTYRTEVPTNLLGGLLGLGSELEIAITVVNGQWVSRSASVASNAGLLAGIGGTCRNL
>NZ_CP023564.1|WP_096798257.1|587822_588275_-|hypothetical-protein
MAAKKLTTLGPKGKGALDTAKWALPLLVAAGRWVSANPEILEKAKQQITQLTKARTGTPEGVLETITVLRGNVDYLTASADDEAEVKQARDWERQLARCEQAALLLKAPGAPGKERRALKKRIGALRSEIVAAFIAEQGEDAVEGDARRR
>NZ_CP023564.1|WP_151904647.1|586046_587744_-|PAS-domain-containing-protein
MQVPGSLSARLDRVRSPVGGTASKQLYFAGFMLSFTALIALSHIELVIAAPYLFALGILVLATVLAMTIRWEALPASWGAVVPVMDIVAVAVTRDLMRDYAVAVSLLTLIPVVWLAARLRSAGVLIGTASVTLLVTVPALVRTELIDSLTIANSLLLPFTVLQIGLLITGGLALLDGRNDQLAQGLREKAALLEAADTSEQLLTSIIDSVDVGIVVVDRDGHDVLMNRTQRRIHELCTPEGVADPDEGLLLLRYPGTSTAIPTEQRPVRRAVLGETFSNYIVTAGPPGRGASFSASARQILDHRGVRSGAVVVFSDVSSYIETVRSQERFVAAVSHELRTPLTSVIGYLELARDDRDLSVEATSHLEVASRNAEQLLLIVQDLLSDQVSRSGTQQLTLRPDRLSEIARDCAESVAPQAQDAGIEIEQDLRETPELPLDAHRMRQAVANLLSNALKYTPREGRVSVHTGVRSNHVELTVVDSGVGMSAKEQTELFTEYYRTPTARESAIAGHGIGLSLTRRIVVAHNGQISVRSILGEGSTFTIRFPLESHAEGADDPGQRDSPTT
>NZ_CP023564.1|WP_096798255.1|584020_585910_-|glycosyltransferase
MRTAVTVVLAVFYALLAVVAFGVSGVFGTLGESLWRDVAVALLTAVAACALTYVSLLLLTFLREVRRPRNSPGDPAELEWHVLVPCRDEENVIAETVSAARSSFPAMHVWVIDDASEDATAAVVRDLMVFDDRVHLISRIAPEARTGKGDALNAAYRIVSEHVDGDEATRHRAIVGVLDADGFLSDNALPMLAGPESFGDESIGAVQLEVWMKNRGDRRPRPDDGRLRNAVGRALVRMQDLEFRTTNSAMQVLRVRTGTVGMGGNGQFTRLSVLDTLTEEHGKPWGKKLSEDYELGLNILHQGMRNHYVREAHVSQEALPFTRRLITQRTRWAQGNMECASALPGLRRSGHLSAAGLLEIHYFMLQPLIMMLNLVLIPLLLILGLTEDPGGFWSASSLATIVATGLFFLVLPYAVWGLVYHRVTDGEVSWPLAVGLGLCNLVYVYLTYVYYLRAAWRALSGSTGWAKTRRNADGRSSAPVILDAALEALPLMRLEELEELSAELEGRSDLGIDFVAGWAIMWPTRASRLERAVAAEDPSAIRDAIGSLRVSSAMVGAARLEQASIGLEQAVARDALEECRDRLPVVLAIGRETVDMLRKEVSVRRALLDTPRQAEPAVTESRMVTVPRS
>NZ_CP023564.1|WP_096798254.1|583662_584040_+|response-regulator
MATALVIEDDDDIRRLLEVVLGQAGYRVSAAANGADGLEALEAQSPDLLLVDVGLSDIEGYEVVRRARPQVGGHIVMLSARPEESDARLGLEAGADEYLTKPFRPRRLREQLAEIIERPVTSGER
>NZ_CP023564.1|WP_151904646.1|582292_583342_+|hypothetical-protein
MTDVDTPAPHRRPWLLTGAILLLVLVVLLGILALRGQGGADRHAAPASSAAATTTAPPYPSAPYSRVDDTTLTVPEKTRFAPGTFWATAGTEYLVSMDLQSVKPEGSGGRSMYLGVTLSCSPQAGGPGISVGGTQNMLTGETTTYSNQGLISVPEDGAIDCSIKASAPYDDVASNGTSFDIDATWNATPVDGEAQASDEKGLPRTIAAGAEETVMSTDLPPDQGGGDDLHALTSLHLTTCTIVNGSREDGRAWCSPNALDKNGSTVTTTLRADLVDDSGTVCQNLGTLSGEADHIDLYRHHRVLSLELDETVPRQPCGETVRVSTSVHNEGPAPLVVHRSNSSLVVVGE
>NZ_CP023564.1|WP_169928776.1|580584_582177_-|glycosyltransferase
MPDPQTSRLDTLRKGLWHLRHGGIAEFRQWWSRQESRRAKPSALANAGDFATLRKGLWHLRHGGIAEFRLWWSRQESRRAKPSALSNTPGASATGSVAVRNSDLARNGFPLPEMRSEPEYEPRPDHVLYLLHNALPNHSGGYATRTHGLLTELGRIGWDVDGVTRLGYPYDMPKMADVPELPASEVVGEVDYHHLLTGRQIEKKNPMHDYVARYTDALLPLARAERPAILHGASNHWNGLAAVQTGRLLGIPSVYEVRGLWEVTRGSRDPEWGRSDQYRYIARMEADAARGATKVLAITQALKTELVERGVDEAKIVLVPNGVDTERFTPLPRDEELAAQLGVAGKTVIGYVGTIVDYEGLDLLLESAATLKRSREDFHVLIIGDGAKLEELQSSATSQGLDDVVTFTGRVPHEEVERYYSIIDVTPFPRLPLPVCEMVSPLKPFEAMAMGKAVIASDVAALAEIVTPGRNGLLHAKGSADSLTGQLELLLDDHELAARLGGQARDWVVAERDWRQLAATVAEVYAEIVE
>NZ_CP023564.1|WP_096798251.1|578893_580588_-|heparinase-II/III-family-protein
MTLDLEAARRQTLVTSVNPDEIKKLLSGVLHMSPHPRWTLPEEPTWLEDPFEDRNWRFQYHMLRWLDPLRRAAAHGDDRAYAMWSRWIHDWVEKNPPSAPTTSWAWTDMSDGIRAQQLCSASTLLAERDPEQLEWLERTIRVHAEHLADPANMGNANHALHQQESLFMCGRVLKDERLWQLASRRMSTLLMEQYDEQGVNAEGATAYHYNNFLWWERALRRFDLENLPRPDGTDRHLQAPEEIAHATRPDGTLVPIGDTDVQNPKQVQSPFVAYVTTNGREGTAPKDLVKVYDAGYVFGRSGWGTRQRPFAEQTFYSLRFGPSRRVHGHPDGSSLTYSAGGVHWVVDPGKYQYGRGTARDHFVSRAAHSLLSIDGRTAFKEPYTELTHRSITSRAHEFVVEDLSYDGIEITRRVIFSTRGEYLVVLDHAASKRQITGVQRWQLGTSVDAEIQGNTVALTSGDRSGVLWFDDGPTEISTITAQDDPFDGYISTGWKQMAPATAVLAERRGTALTFVTVLSAGSMTPPTVQQVPVAVPGRIVLDVTINGTTERILLSPTAVSFPAI
>NZ_CP023564.1|WP_096798250.1|577426_578680_-|UDP-N-acetyl-D-mannosamine-dehydrogenase
MSPNVPLDTVAVIGLGYIGLPTAAVLAQAGKTVIGVDIKQSNVDAINAGKVPFVEEGLETVVAGTVAQGKLSAQTETPVADAYIVSVPTPFKGDHDADLSYIEAAAAGIAPKLSGGELVVLESTSPPGATEHMAQVILEARPEFTTEPNLPNSLYFSHAPERVLPGRIMIEMVENDRIIGGLGKEAGELNRELYASFCHGELLVTDARTAEMAKLTENAFRDVNIAFANELSIISERQGIDVWELIALANHHPRVNILQPGPGVGGHCIAVDPWFIVSADREYSNLIRTAREVNDSKPELVLDKVMKKADKLKNPLVAALGIAFKANIDDLRESPSKDIALALTDRLDHGTVLVVEPNIEELPKEFAGKDNVQLAELDDAVERADIVLLMVDHDPFKEFDREKLREKVLIDTKGLWR
>NZ_CP023564.1|WP_096798260.1|594556_595309_+|hypothetical-protein
MASTRIRRLPAVVLATVGLLAAGHIGATLAYTGPDTPLRAALQPALNRYFLGPLDQGWNLFAPGPYSQDEYMLVRACISEFDVCAGGADAGAEFTPWRNITADEAEAVQYNIFANRESRQSKVVHGRLWPAANKLTDEQRKQAAANHIDGDPVFGVDLYSPEAGEGIASDQLNNLRTYQRLEDAAVGLATLTLQEEYGDSVTLVEVRMLREAVPAFDERHDPPEEPAQQWTTIGWRPAMEFDDDVKAAWS
>NZ_CP023564.1|WP_096798261.1|595305_596397_+|HTTM-domain-containing-protein
MSASTPIRSWVTAQRHLPSQLLGRIVTWFIADRHADYGLAVMRIASGSFLLGWLLLNLPIASRIWGPGSAYWQPYREILGYNAPFNALQNAGPGLFWLWYLVTIALVVAFLLGWRTRFVTPLLFIAYTTLNGQNTPVSDGGNYFIRIMLLYLILIDVSRRWSLDSRRRARSGREETQTGSVLHNIGLCLVVAQICTVYLEAGLYKVQGTLWQNGTAVYYPLQSVAYGAFPPLADLLTHWAFPVVIATYVTVLAQIAFPFLLFHKVTRRIALVVLLGMHLSIAVIMGLPFFSGIMASADAVLVSGATWIAIVAWLRTALTENRLSRTLVEKLPRRAGRGRRASTSPKPAPAPDPQGAEEEPSRV
>NZ_CP023564.1|WP_096798262.1|596467_597895_-|PepSY-domain-containing-protein
MPESPAPRHWLGPLLLRLHFYAALLVGPFLLVSAASGALYAVSPQVEQLVYADELEARTEGPALPLAQQVAAAQELVGEGAQVSAVRPAPEPGDTTRVMYADPSLGESESRAIMVDPATAEIQGDLTVYGTSGSLPLRSWIDQLHRNLHLGEAGRLYSELSASWLGVIAVAGLGLWVRRARRSRRKRDLLRPDLHARGYRRTLSLHSSVGVWVLLGALFLGATGITWSRYGGGNVGVVREALGFTTASVSTELPESEQAVEGEEPASEEAGHGEHGEHGGHGAAAPAAEQKGPSGGIEAIDDVLAAGRADVIDTGRIEIRPPADAGSAWVIEEIQRSYPTKVDAVAVDGESLEVVDRYVFAEADIASKLTRWGIDLHMGVLFGVVNQLVLFAIASALVAMIVWGYMMWWQRRPTRGGAGVGRPPHRGALRRAPWWGVALVLLTAGAAGLLLPLVGASLVVFVVLDAVVGRVRAGR
>NZ_CP023564.1|WP_096798263.1|597902_598700_-|class-F-sortase
MTSPGENRRGGGRRLTIAALGALAVLGALLVGYTLTSQVGEPPQPELRTAAQASDGGGDAQASDDGGTVPGPSAEGAATPTAADEPAEPTEPAEPAEPAEPAEPAEPEEPLAPALTRSEPTTLRIDSLSLEAEVFPLGLGPDGALLAPSGERAHDPAWFDGSPTPGEVGPSVIEGHVTWGGDPSIFFELGALRSGDRVEVDREDGTTATFEVYDTARFAKDAFPTVAVYGRTDGPELRLITCGGELDDQGHHLDNTVVFLRLIEN
>NZ_CP023564.1|WP_096798264.1|598701_599475_-|CHRD-domain-containing-protein
MRTMTKRLLPLLAATAAVGMLSAPAALAEGHGGDHGSTTLEAHLTELNQSGASGTAWVTLEGNEVTVKMENTGLLADSPHAQHIHVGGTNSCPDPDAKGNGENGALQVSDAHHAYGDIVASLTTEGDTSPDSGLAVERFPVGDAPYERTFEVSDQVAADIAAGKGVIVVHGVDHNGSGAYDGDVKSDLDPSLPSEATDPAACGELEVAQMQEWPDGGAATGGGSTAGIENVGALAAGGGLLTAAAAGAFALRRRTQR
>NZ_CP023564.1|WP_096798265.1|599878_600490_+|hypothetical-protein
MSTSTTSPQRGRKIRALLAGGLVLGVGAAVTLAAWTDEEWAIGNFGAGSFNIEGSTDGTDFADHNSEAGAAVLPFEIDAENLSPGDSVAAPFVVRTDAATTYGATVELTSAAGEGTIAPDLTYGISQVGATGECTEGATGTPIVPAGTSVDAITGAAPFTLEAGAAGAAGAPVVLCFEVTAGETLQQGDTGSATWEFTATSVE
>NZ_CP023564.1|WP_096798266.1|600540_601158_+|hypothetical-protein
MRRRRRWRQFRALLAGGVAFGLGASVTMAAWNDTETGTAEFRAGEFQLEANIDGTWNATRQMTFTSGAMFPGAVTYAPVRLRTTPTTTVPGDMTVTGTGRTSGSGAIADSLEYRAVIQPVTGTTPPACGAGAFTSSATYAFGSATSWQAMSSGVTSPTVRRLEAAQRSTLQYCFEVRLRANTPNSAQGTRAGYTWTWDATSVAPG
>NZ_CP023564.1|WP_096798267.1|602515_603043_+|hypothetical-protein
MTTSQVRRLRHHPSADDDRPATRWRHGARPVAGVLALLLLAATLLGGTGALGRATEGMWTDAMWTAPKPADGSFTGLQVGPVQAYSCTAALWTSATVTWQRPAGTPSGVVSYRVTLQRGSTTQTTTQTATTFEYSRPAGNFDAVTLTVQPFIGEWNGTSQSMRLEAVPLVGMRCP
>NZ_CP023564.1|WP_096798268.1|603191_604991_+|glycoside-hydrolase-family-2
MTLSATRHGGTHPRPTLQREDWESLDGPWSFAHDDADRGLAERWYAPGAAAGEVFDRTISVPFVPESEASGIHETGFHPVVWYRREITATVRPGRRVLLHLGAVDHEAHVWVDGRLAGHHVGGQTAFTCDLTDLLEPGEEHVVVVRAFDDPHDPELPRGKQDWREEPHGIWYHRSTGIWRSVWLEQVPDQHFTGFHWEFDMPRARVEVSLRLARRPLPGTTVRATLTAGEERLGAVEIAAHDTRVQGVVDVPAVRNTQDRDRLLWSPEHPHLIDVALEVLVDGEVVDEAASYLGLRTTGIDRGHFLLNGEPYFVRSVLEQGYWPSSHLTAPTLEAYRQEVELIKELGFTAARIHQKVEDPRFLFWADSLGLLIWGETANAYAYSPRAAAALTSEWTEIVEQCRPHPSVVTWVPVNESWGVRDLADSAPQKDLTIALTALTRALDPTRPVISNDGYELTGGDVIALHDYTTDAAALAANYASEDAAEATIAGRGPQRRRPVDDAAQHLNPDAPVMITEFGGIAYAAEGTWGYATVSSPEEFEQKVGGLFAALNDSPVLAGHCYTQLTDTLQEANGLATADRRPKLDAAVIRALVTGRDQA
>NZ_CP023564.1|WP_096798269.1|604987_606874_+|glycoside-hydrolase-family-127-protein
MTGRLRRPAAQLPLGQIRPRGWLERQLRLQAAGITGRLPEVWADVGPDSGWLGGSGESWERGPYYLDGLVPLAHVLGDEALIAQAEPWIEGMLASQREDGSFGPAADEDWWPRMVAAKVLIQHAEATEDSRVAPFLLRWCEHLREELPGRPLSGWGEVRGADLALAVAWVHERIDQAWLVDLLDLVLEQTFDWNAYLTGDLVTGPARVFEHRTHGVNVAMGLKTAAAASLRGDLDGHRERTEAAFAALERWHGQAHGWFAADEWLGGREAVAGIETCLVVEMMHTQEVLSRLFGDGVQGDRLESLAMNLLPASSDPRMLAHQYHQQGTQLEASVARRDWSCSSDGANVFGLEPHFGCCTANLHQGWPKFAASLWARDEDGGLRAVAYAPAVVETALVPGGGAADPSADGAVPVRIEVETDYPFEESVRLTVSLDGPALFPLRLRLPQWCDEPALTLDGERVEILDRGDGHVEIERDWSGTTALLLTLPMRPRIVRRERQAAAVHLGPLVMVASPGETWRSVPDAPGLGEWEIHPRTSWNWALAELENAGTWPVERGPVPEAPFALSRATVLRATGCDVPHWLRDGASAAPPPPSPVMDHGPVHDLELVPYGTARLRVMEFPVAIGRRD

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Crispr_ID: NZ_CP023564_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023564_3

631064-631178

Orphan

Consensus_repeat	Method
ACCGTGTCGGAGTCACGAACAGGGGCGAATG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023564_3

>merge|NZ_CP023564|3|631064-631178|CRISPRCasFinder
ACCGTGTCGGAGTCACGAACAGGGGCGAATGACGCGGTGATTCCCCCCGGTTCGTCACCCTCGCAGGGTGAGGGCGGGGGCCGCACCGTGCCGGAGTCACGAACAGGGGCGAATG

>NZ_CP023564|3|2|631064-631178|CRISPRCasFinder
ACCGTGTCGGAGTCACGAACAGGGGCGAATG	ACGCGGTGATTCCCCCCGGTTCGTCACCCTCGCAGGGTGAGGGCGGGGGCCGC
ACCGTGCCGGAGTCACGAACAGGGGCGAATG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023564.1\|WP_169928778.1\|631409_632522_-\|ROK-family-protein	unknown	unknown	gnl\|CDD\|224851
NZ_CP023564.1\|WP_096798287.1\|626211_627252_+\|MoxR-family-ATPase	unknown	unknown	gnl\|CDD\|223786
NZ_CP023564.1\|WP_096798281.1\|616838_618839_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|235906
NZ_CP023564.1\|WP_096798284.1\|621376_622048_+\|TetR/AcrR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|366102
NZ_CP023564.1\|WP_096798292.1\|634388_635150_-\|DUF624-domain-containing-protein	unknown	unknown	gnl\|CDD\|227865
NZ_CP023564.1\|WP_096798295.1\|637111_638338_-\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP023564.1\|WP_096798298.1\|646630_647995_+\|APC-family-permease	unknown	unknown	gnl\|CDD\|129987
NZ_CP023564.1\|WP_096798279.1\|614581_615766_-\|alcohol-dehydrogenase-catalytic-domain-containing-protein	unknown	unknown	gnl\|CDD\|176243
NZ_CP023564.1\|WP_096798293.1\|635146_636115_-\|carbohydrate-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223472
NZ_CP023564.1\|WP_169928780.1\|643797_646545_+\|ExeM/NucH-family-extracellular-endonuclease	unknown	unknown	gnl\|CDD\|225249
NZ_CP023564.1\|WP_169928779.1\|641126_643604_+\|5'-nucleotidase-C-terminal-domain-containing-protein	unknown	unknown	gnl\|CDD\|223808
NZ_CP023564.1\|WP_096798286.1\|624745_626077_-\|LPXTG-cell-wall-anchor-domain-containing-protein	unknown	unknown	gnl\|CDD\|380149
NZ_CP023564.1\|WP_096798288.1\|627248_628604_+\|DUF58-domain-containing-protein	unknown	unknown	gnl\|CDD\|224635
NZ_CP023564.1\|WP_096798291.1\|632781_634392_-\|extracellular-solute-binding-protein	unknown	unknown	gnl\|CDD\|270299
NZ_CP023564.1\|WP_096798283.1\|620422_621247_-\|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl\|CDD\|366542
NZ_CP023564.1\|WP_151904810.1\|639084_640530_-\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224172
NZ_CP023564.1\|WP_096798294.1\|636119_637112_-\|sugar-ABC-transporter-permease	unknown	unknown	gnl\|CDD\|226666
NZ_CP023564.1\|WP_096798285.1\|623380_624658_+\|MFS-transporter	unknown	unknown	gnl\|CDD\|340863
NZ_CP023564.1\|WP_096800902.1\|622278_623145_+\|formylglycine-generating-enzyme-family-protein	unknown	unknown	gnl\|CDD\|335469
NZ_CP023564.1\|WP_096798282.1\|619280_620426_-\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745

Protein	Function_ID	Function_description	E-value
NZ_CP023564.1\|WP_169928778.1\|631409_632522_-\|ROK-family-protein	gnl\|CDD\|224851	COG1940, NagC, Transcriptional regulator/sugar kinase [Transcription / Carbohydrate transport and metabolism].	5.38597e-31
NZ_CP023564.1\|WP_096798287.1\|626211_627252_+\|MoxR-family-ATPase	gnl\|CDD\|223786	COG0714, COG0714, MoxR-like ATPases [General function prediction only].	1.54939e-87
NZ_CP023564.1\|WP_096798281.1\|616838_618839_+\|hypothetical-protein	gnl\|CDD\|235906	PRK07003, PRK07003, DNA polymerase III subunit gamma/tau.	0.00385476
NZ_CP023564.1\|WP_096798284.1\|621376_622048_+\|TetR/AcrR-family-transcriptional-regulator	gnl\|CDD\|366102	pfam00440, TetR_N, Bacterial regulatory proteins, tetR family.	2.72627e-13
NZ_CP023564.1\|WP_096798292.1\|634388_635150_-\|DUF624-domain-containing-protein	gnl\|CDD\|227865	COG5578, COG5578, Predicted integral membrane protein [Function unknown].	5.58094e-13
NZ_CP023564.1\|WP_096798295.1\|637111_638338_-\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	5.90546e-46
NZ_CP023564.1\|WP_096798298.1\|646630_647995_+\|APC-family-permease	gnl\|CDD\|129987	TIGR00909, putative_amino_acid_transporter, amino acid transporter. [Transport and binding proteins, Amino acids, peptides and amines].	4.31027e-29
NZ_CP023564.1\|WP_096798279.1\|614581_615766_-\|alcohol-dehydrogenase-catalytic-domain-containing-protein	gnl\|CDD\|176243	cd08283, FDH_like_1, Glutathione-dependent formaldehyde dehydrogenase related proteins, child 1. Members identified as glutathione-dependent formaldehyde dehydrogenase(FDH), a member of the zinc-dependent/medium chain alcohol dehydrogenase family. FDH converts formaldehyde and NAD(P) to formate and NAD(P)H. The initial step in this process the spontaneous formation of a S-(hydroxymethyl)glutathione adduct from formaldehyde and glutathione, followed by FDH-mediated oxidation (and detoxification) of the adduct to S-formylglutathione. MDH family uses NAD(H) as a cofactor in the interconversion of alcohols and aldehydes, or ketones. Like many zinc-dependent alcohol dehydrogenases (ADH) of the medium chain alcohol dehydrogenase/reductase family (MDR), these FDHs form dimers, with 4 zinc ions per dimer. The medium chain alcohol dehydrogenase family (MDR) has a NAD(P)(H)-binding domain in a Rossmann fold of a beta-alpha form. The N-terminal region typically has an all-beta catalytic domain. These proteins typically form dimers (typically higher plants, mammals) or tetramers (yeast, bacteria), and have 2 tightly bound zinc atoms per subunit.	0
NZ_CP023564.1\|WP_096798293.1\|635146_636115_-\|carbohydrate-ABC-transporter-permease	gnl\|CDD\|223472	COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].	2.0931e-62
NZ_CP023564.1\|WP_169928780.1\|643797_646545_+\|ExeM/NucH-family-extracellular-endonuclease	gnl\|CDD\|225249	COG2374, COG2374, Predicted extracellular nuclease [General function prediction only].	8.07243e-119
NZ_CP023564.1\|WP_169928779.1\|641126_643604_+\|5'-nucleotidase-C-terminal-domain-containing-protein	gnl\|CDD\|223808	COG0737, UshA, 5'-nucleotidase/2',3'-cyclic phosphodiesterase and related esterases [Nucleotide transport and metabolism].	5.57067e-72
NZ_CP023564.1\|WP_096798286.1\|624745_626077_-\|LPXTG-cell-wall-anchor-domain-containing-protein	gnl\|CDD\|380149	NF012181, MSCRAMM_SdrD, MSCRAMM family adhesin SdrD. Features of this protein family include a YSIRK-type signal peptide at the N-terminus and a variable-length C-terminal region of Ser-Asp (SD) repeats followed by an LPXTG motif for surface immobilization by sortase.	3.15773e-07
NZ_CP023564.1\|WP_096798288.1\|627248_628604_+\|DUF58-domain-containing-protein	gnl\|CDD\|224635	COG1721, COG1721, Uncharacterized conserved protein (some members contain a von Willebrand factor type A (vWA) domain) [General function prediction only].	3.49941e-20
NZ_CP023564.1\|WP_096798291.1\|632781_634392_-\|extracellular-solute-binding-protein	gnl\|CDD\|270299	cd13581, PBP2_AlgQ_like_2, Periplasmic-binding component of alginate-specific ABC uptake system-like; contains the type 2 periplasmic binding fold. This subgroup includes uncharacterized periplasmic-binding proteins that are closely related to high molecular weight (HMW) alginate bining proteins (AlgQ1 and AlgQ2) found in gram-negative soil bacteria. The HMW alginate uptake system is composed of a novel pit formed on the cell surface and a pit-dependent ATP-binding cassette (ABC) transporter in the inner membrane. The transportation of HMW alginate from the pit to the ABC transporter is mediated by periplasmic HMW alginate-binding proteins (AlgQ1 and AlgQ2). Alginate is an anionic polysaccharide that is made up of alpha-L-mannuronate and its 5'-epimer, alpha-L-guluronate. Alginate is present in the cell walls of brown seaweeds, where it forms a viscous gum by binding water. Alginate is also produced by two bacteria genera Pseudomonas and Azotobacter. AlgQ1 and AlgQ2 belong to the type 2 periplasmic-binding fold superfamily. PBP2 is 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. However, unlike other bacterial periplasmic-binding proteins that deliver small solutes to ABC transporters, AlgQ1/2 can bind a macromolecule and may have specificity for either sugar or a certain type of polysaccharide.	6.35485e-113
NZ_CP023564.1\|WP_096798283.1\|620422_621247_-\|sugar-phosphate-isomerase/epimerase	gnl\|CDD\|366542	pfam01261, AP_endonuc_2, Xylose isomerase-like TIM barrel. This TIM alpha/beta barrel structure is found in xylose isomerase and in endonuclease IV (EC:3.1.21.2). This domain is also found in the N termini of bacterial myo-inositol catabolism proteins. These are involved in the myo-inositol catabolism pathway, and is required for growth on myo-inositol in Rhizobium leguminosarum bv. viciae.	2.49143e-19
NZ_CP023564.1\|WP_151904810.1\|639084_640530_-\|FAD-dependent-oxidoreductase	gnl\|CDD\|224172	COG1252, Ndh, NADH dehydrogenase, FAD-containing subunit [Energy production and conversion].	8.87121e-120
NZ_CP023564.1\|WP_096798294.1\|636119_637112_-\|sugar-ABC-transporter-permease	gnl\|CDD\|226666	COG4209, LplB, ABC-type polysaccharide transport system, permease component [Carbohydrate transport and metabolism].	1.34434e-129
NZ_CP023564.1\|WP_096798285.1\|623380_624658_+\|MFS-transporter	gnl\|CDD\|340863	cd06173, MFS_MefA_like, Macrolide efflux protein A and similar proteins of the Major Facilitator Superfamily of transporters. This family is composed of Streptococcus pyogenes macrolide efflux protein A (MefA) and similar transporters, many of which remain uncharacterized. Some members may be multidrug resistance (MDR) transporters, which are drug/H+ antiporters (DHAs) that mediate the efflux of a variety of drugs and toxic compounds, conferring resistance to these compounds. MefA confers resistance to 14-membered macrolides including erythromycin and to 15-membered macrolides. It functions as an efflux pump to regulate intracellular macrolide levels. The MefA-like family belongs to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	2.55399e-47
NZ_CP023564.1\|WP_096800902.1\|622278_623145_+\|formylglycine-generating-enzyme-family-protein	gnl\|CDD\|335469	pfam03781, FGE-sulfatase, Sulfatase-modifying factor enzyme 1. This domain is found in eukaryotic proteins required for post-translational sulfatase modification (SUMF1). These proteins are associated with the rare disorder multiple sulfatase deficiency (MSD). The protein product of the SUMF1 gene is FGE, formylglycine (FGly),-generating enzyme, which is a sulfatase. Sulfatases are enzymes essential for degradation and remodelling of sulfate esters, and formylglycine (FGly), the key catalytic in the active site, is unique to sulfatases. FGE is localized to the endoplasmic reticulum (ER) and interacts with and modifies the unfolded form of newly synthesized sulfatases. FGE is a single-domain monomer with a surprising paucity of secondary structure that adopts a unique fold which is stabilized by two Ca2+ ions. The effect of all mutations found in MSD patients is explained by the FGE structure, providing a molecular basis for MSD. A redox-active disulfide bond is present in the active site of FGE. An oxidized cysteine residue, possibly cysteine sulfenic acid, has been detected that may allow formulation of a structure-based mechanism for FGly formation from cysteine residues in all sulfatases. In Mycobacteria and Treponema denticola this enzyme functions as an iron(II)-dependent oxidoreductase.	6.63084e-70
NZ_CP023564.1\|WP_096798282.1\|619280_620426_-\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	2.98128e-58

>NZ_CP023564.1|WP_096798288.1|627248_628604_+|DUF58-domain-containing-protein
MTARPGTILRPTGRGGVVLGLCLVLWVLGDLARVNPARQIAAALLIMLVIGAIGILVSSVGLRPRRYLVDDAVPVGGSARVMLLLEGTPWITVVPLGRGIVREDLPVELGDQGDLPLAARMPHVLRVGRRGRHDLGPYSIIVRDLLGLFHLRRTVDDGLHLTGLPVVGTMEPAAEQVTGISREGAIGAIASQGVGEISPIPRPYASGDDIRRIHWRASARTGQLMTREDEPSVGQSAVIVLDTSQRENPSGEVEDALVSHAATVLDALGLNGWEVRIVDASGDEITRTGRRRGIPGPSPLGSEADAVEQRASLLALADVDFDDDASGGIGHDHAAGHAALAIALGPDDGDPFSGLELDRFAGRAAHRTAIALRPALEDQGEVPASTPPARRIGPGDGEDFGRAHEQHRAELAAVRDRHAPVRSQLGAWTLVRGTAADSLTALLTADEETAR
>NZ_CP023564.1|WP_096798287.1|626211_627252_+|MoxR-family-ATPase
MTQDDLAVQAPQDPTDAHSRSAPPTLTESQVQEIAAEAEGIIAEIATIVEGKDEVARTAVLVLLAGGHLLIEDIPGVGKTMLAKSLAASLGAARHRIQFTPDLLPGDVTGASVFNQATGEFEFRPGAVFTQILLADEINRASPKTQSALLEAMEERQVSVDGTTYPLAEPFMVVATANPVEMEGTYRLPEAQRDRFLAQTSMGYPVPGAEARMLAAQTGPIREGDRDVIDAVVTRTSPERIAAHIAQVRGVFASPLILDYVVRLAQATRSHPQVTLGASPRAAVHLVRAAKAKAALAGRIFVTPQDIADVIMPVWRHRLHLTPQALSRGASAEDLVDQVLRGTPQA
>NZ_CP023564.1|WP_096798286.1|624745_626077_-|LPXTG-cell-wall-anchor-domain-containing-protein
MSIRRGQATVRLGAGLALALTCAGAPAIVLAGPTAPAAAEVTDCAPDAAPSASATSTTLDGTVEVSGDCFPPRQQGQIEIFIQGDDASRQVKQVQTESSQSVSASFEPEVAGDYTAVITVIGETADTSFTVDPSQQPQDPPTDPPTDQPSEPTEEPTEDPTTEPTEEPSTPPASEEPSTPPPDEGDDTTDEPGAGDSTEDDDSDSGDGDGTDPGDDSSTGGGTGNDDTGNDDTGNDDTGNDDTGSDGTGPGTGGDDGSDSSTDAPDGGDTGSTRPGDGQDSSTSSPDSPSSETGDEAQDEDEPDPSAADRPSPSVPDSETSVPSSPGTSDFPPAPPKHAAAQKKQAALAVLVASEFAHGVSGGAVGTAPAASDAGTSGDDSTGDGSSSGGASEGGDASGVGAASDGGGELAETGTDVSVPAGLAGIALLSGAGLLWHHRRRQD
>NZ_CP023564.1|WP_096798285.1|623380_624658_+|MFS-transporter
MPRSRRRSSPTNLQAPRRFGPLRDKHSRPYLMTAGLSMMGDNIEHVITYWVLWELFASPWLVGFQVISHWLPFLLFSVLFGGLAEKYDCRRIIQVAQCLFAFVSLSWGLLLLTGTLEMWSACVLLVLHGMAGALWGPAEQLMLHDFAEPAELPSAVRLNATFKSLGVLAGPVVGSVLLLALGPTGGIFANVLFYLPMTLLMLRTPFTGHVRSGHVRRERVSILDTPRVLRTVGGDKVLVGMIALAGLIAVCVGASLQVAMPNFAEVLGAGEEGGIGYGALLFANGVGGVVGGFLLEATGILRADVRGAVVAAVMFGLTSLVVATTTHYPVALIALVIGGVANLAATSIGQALVQLRAPADQRGRVVGVYSMIGSGMRTGNGITLAWLGALLGVSGAVAVGGLALAVGALLIGLLIALQTRRGLAA
>NZ_CP023564.1|WP_096800902.1|622278_623145_+|formylglycine-generating-enzyme-family-protein
MPAGSFTMGDSSGDRNRADGETPRHQVALSAFEIDATTVTNDDFARFVEATGCITEAESFGFSAVFHLAIDAPPEDVMGPATGTPWWSGVKGADWRHPGGRFTDLEGRGDHPVVHVSWNDAQAYCEWAGRRLPTEAEWEYAARGGIDGAKYPWGDQEVDEGGWRANIFQGEFPRRNTGEDGFPTTAPVRTFAPNGYGLWQSVGNVWEWCEDRFHPATYRRGTTAEKRTTVTDPVGPADGQARVMRGGSYLCHDSYCNRYRNSARSQNTPDSSMGNAGFRTVSRRGAER
>NZ_CP023564.1|WP_096798284.1|621376_622048_+|TetR/AcrR-family-transcriptional-regulator
MSTEDPAPAVPGGTPEATPSADGTARPAARRIGRAGSYSKGIARRQEILDRAIEVFRERGADGTSLRRIAESIGVSHGALLHYFSSREELLVAVYEHAESPKGDESEDREPERSVHVMTNAAIANLEVPGLVQLYSTLVATALEGETGPAKEYFTARFERVRCSLEAKLREDQESGLVRRDVDPARTAALIVAASDGLQIQWLLEPSIELKETLETFAVLLAP
>NZ_CP023564.1|WP_096798283.1|620422_621247_-|sugar-phosphate-isomerase/epimerase
MALPLASVQLYTLAAEFSADMNGSLDKLAKIGLKNVEAFDFVRRPAEIRAALDASGLASPTGHAPLLSDELWTPDGSIPTPANEVVFEAAAEIGMTTVIDPMVPTERWITEDGVKDIAERLNTASEKAKEFGLKVGYHNHAQEFLADFDGQTAYQRFLSLVDPSVAIELDLYWALVGGQDVVALVQELGDRLVAIHVKDGIKPETNPFAPDAPKFSSKSLDQRHAGEGEVPTIDAMKAATNVQYAVIEYDNAPGDVFEDVENSYRFLIDGGLAA
>NZ_CP023564.1|WP_096798282.1|619280_620426_-|Gfo/Idh/MocA-family-oxidoreductase
MSIAPKPFSGPVGVGFIGVGVISDTYLENLNSFPDVEVLILGDIDAERAAAQAEKHGVPAHGSAQDVLDHPDVQVVVNLTLPATHAEISSAAIAAGKHVWTEKPLGLDRESTAALLKQADEAGLRVGCAPDTVLGAGVQTAKRAILDGLIGRPLFAQTSMQWQGPEVFHPNPGFLFAKGAGPLLDMGPYYFTTLVSLFGTVEKVAAVGLKALEERTIQVGDKAGTTFPVEVPSTISVLTQFEGGQTGTSLLSFDSPLARQGIVEIHGTEGSLVVPDPNMFEGRIAYVRPFESFGERPPEQEWIEVTQEGPTTGRGLGLLDMVRAIHTGRPHIATGEVGYHVLDVMLSAEESAASGEFVTVNSSVSEIPAVAADFDPLASTL
>NZ_CP023564.1|WP_096798281.1|616838_618839_+|hypothetical-protein
MTRDASRPVRQRVRIALRDLAYSPPVRGLARQVEDRPAAAGAIEKRGRGELLRRIASESLPAGQFYARLTILNWKKHRGADVRLLERGEVVYGNRIQAPPEGAPLEYRNIVVTSSDPADFTLDPPARYRLDISRGAFSTPEQDSYDQRYGVRRQDGLYSSVRGNTTSPTRLLVTFPGFPPANSRVSYAVSYLKALGDEDLADTLMVCFQDRYGVAGTYMVHDNAGQPLTGRITAAITALMQRHGIAEEDVLLFGASKGASIAAMTARCLPGARQVLVVPQMSLPYYLAKPVLRGGLFRDRALWEVEQPGILMRRHLAEGRRIDWFYSDSDESSNASVVEYARDAEGLTKHRIGGAHASVAKRSMPTVLSLLRSFAHGADGGDTGSAEPAGMPLEIVELTSSVRGDQVSHRVQFADDSVPAAANVYLEGMLGRTRFRQLLSPGRDRAARWTAPAQRTDPTLHPARFTRVVAFDGTPQVRAAAVPPVDAGAEPPVDPAGAAGAAGAAGAGDVGGAGPVGRHPDSTPTPLTCDATEPRDYALLAAAGAPSARVRYLSSMVDPTGETVELVLVPSLEEAGSAVGGDWGLGAAGSGAGLGAAGPGGSVARFVMEALSPWHDLPQLMRRLAIACEVEQVRVIVTDSDITPDQIRDLEASGWPAVTVHDTRSA
>NZ_CP023564.1|WP_096798279.1|614581_615766_-|alcohol-dehydrogenase-catalytic-domain-containing-protein
MKAVTWQSTHQVSVQDVPDPQILDAGDAIVRITSTAICGSDLHLYEVLGPYMEPGDVLGHEAMGVIEQVGSGVTRVRRGDRVVVPFNISCGHCWMCTQGLQSQCETTQVTEHGSGASLFGFSKLYGQVPGGQAELLRVPHAEYGLIAVGSDLPDERYLFLSDILPTAWQGVKYADVPDGGTLAVIGLGPVGQFAARIGVHLGSRVFAIDPVPERRAMAARHGVEVFDQGPDGVKTIREATDGRGPDAVVDAVGMEAHGSPVARAAHQVVGHLPKPVGQRAMETVGVDRLAALHTSLDLVRRGGTVSLSGVYGGVASPMPLLSMFDKQIQLRMGQCNVRAWIDDLLPLVEDPADPLGVTDLITHRLPLEEAASAYAMFQKKHDGCIKVVLDPARR
>NZ_CP023564.1|WP_169928778.1|631409_632522_-|ROK-family-protein
MTPSDPGARRAGADTTLVRHLNRRTVLTTLRSHPDITLSTLGSLTGLSRATLSAVLEELTERGLLEEHAPATGGSGRPARRYAFRATAGYVLGLHFTPNQVRAVVTDLEGQVVARERTEVPPSVPAPERLARARALAETATSQAGPVWSVGVATTGVVGPEGRVLRSSQIAGWTGLDLVGTVRGWYGRDAVAGNDGTLAALGEKWQGAARYADDVALILSGRPSGQGIVLGGRAHHGRSGAAAELGRLLQDQTWNAAAVLDEAGRTAQDVFRAASEGEEEASRLAAHLAHHTARAASVLVSVLDPQLVVIAGELTVGGRPFLEAVRLQLETMCINVPAVVLSELGDDAVPLGAARLALDALEEKEYALEG
>NZ_CP023564.1|WP_096798291.1|632781_634392_-|extracellular-solute-binding-protein
MTISPFTRRTVLATSAVLASSAALAACGGGSESTDTSEKIDNPDDNINTEGMPIVDGPVKISLMSRRPNTTAEDWNTIAAAKEAQSITNIEVDWGLVAEEATAERRNLMLTSGDYPEAFYRSGVPGGDIAKYGEQGVFVALNDLIEKYMPNLKARLEETPALRTGLTFPDENIYSLPGIYDPTTLGLRYQTKLWARQDWLDAAGMSTPETVDEYRAFLEEVKGTQKGAVPLGGQGLGSIFASLYGTFGIANQGTDAGAAVDLDPETGAVRYYPTSDGYREMLTFLHGLYADGLLQQDIFATDFAAFTAAGTDGKLGSCAIQAPAGYFGKVGESYAALKPLVRSAGDEPAWHAVRSELSSIGNFVMTDNCEHPVEMARWMDFWYSEEGAKLFFLGVEGESYEMVDGRAELLPAITEAASIDEGLQEHALYLGGWYPGWATGDWFRGVETSEQSTEGAKVVEPFALKEVWPAFTFSAEESQNITTMGNDITKYADESVAAFITGERSLDEWDDHLATFDTIGLADYVATHQTAHERRS
>NZ_CP023564.1|WP_096798292.1|634388_635150_-|DUF624-domain-containing-protein
MSAPTRGAAGALVGGLDALLRRAVQLVWLNLWWTLFTLRGGILLGIGPATVGAHAVASAWARGEREVDVRGTMSACWHRHRRLAAPAGLLALALTASLALTWWLSRGQAPIPAAITQGLVLLAALLLAATLPYLALVIERTDGRGAPLTRTSHLFAAGLALGMSRPVLTLALMTIWIGWPVLLLASGWPGLLPVLGVAIPLAASARCLERVLPRSASAPPRFPPTDTDHDHQTDTDTDSDHAPHPMHVSERTS
>NZ_CP023564.1|WP_096798293.1|635146_636115_-|carbohydrate-ABC-transporter-permease
MTTTTEPRDRLATDRLDGSRVIHKAVGSRDDTWFDRLNVVFVVLIVLVIGYPLWFVVIASISDPLAVQSGKVWLWPVEITTAGYERVFGHSAIWIGYRNSIVYTVVGVAVHLALVLPCAYALSRRHMVGRTLVTWYILFTMLFSGGIIPTYLLVRNLGMLDTMWAVILPGAVGAWSILVGRAFFTQTVPEELGEAAKVDGASDLQTFVRIALPLSLPIIVTLGLFHGVGLWNEYFKALIYLSDRDKFPLQLVLRELLIVSQDPSAGGGAGQGGDAGSIVEQVRLAGLIKYAVMILASLPLLIIYPFLQRFFTQGVLIGSVKG
>NZ_CP023564.1|WP_096798294.1|636119_637112_-|sugar-ABC-transporter-permease
MSALSPASEAPPTAPGPSGTAAVRPAPPSRRRRLRRGFAASWQLYLLAAPALVFFLVFNYVPMYGVQIAFKEFIATRGITGSPWTGLENFERFFSSFYFWRLLRNTLILSVYQLILFPLPIILALSLNELRSRIFKKFTQTLTYAPHFVSTVVVVGMLFAFLDPNTGLINHVLGLVGIDPIQFMQSPAWFRHLYVWSGVWQSLGWGTIIYLAALAGVNPELHQAAEVDGANRLQRIRHVNLPAIMPTVVILLILDFGSFMSVGFEKVLLMTNDLNAETADVIQTFVYETGLLQGQYSYAAAVGLFDSVINILLLITVNHLARRFSENSLW
>NZ_CP023564.1|WP_096798295.1|637111_638338_-|Gfo/Idh/MocA-family-oxidoreductase
MISPVFAPDSVRVGLVGSGQRAASYLRNVPSDMMDAVRLAAIADPHRSQREAFAELFSATPELLDDGVEMIRERELDAVIVATPNDRHVPYAIAAMERGLPLLVEKPVATTLEGLTALWRADRARESGRTVVGFVLRYTPFYQRVREIVRSGRLGEVLAVQADENLGTGLTMVQYQGWRQDVGRSGGWMLEKCCHDLDVLGYVLDSRPVRVQSMASARVFRPRPEGEQLARFQPSAGTAEMDFGTEAERAALQETMQHSPYSPSGLPDRQVATIEFASGVMATFTSVMAQPRSTRRLRIFGTEGLLEGDLSARSIELSFPDPAGGSSMSTESERVEIGASGHHGGDEVLCDTFWRLAAGQDVVPRADLEDGIDAVLCAMALQDSARTGQGVEIDPLRRTVLGAGELVG
>NZ_CP023564.1|WP_151904810.1|639084_640530_-|FAD-dependent-oxidoreductase
MPLPFVSRRPTVPAKDGASWPHVVILGGGFAGAHAVGALRDARVRVTLIDRNVYKTFQPLLYQVATAGLNPGDVTMFLRGLSLKVPNMRYRQGEVEGVDPERKVVRLDEGQKGQHEISYDYLIVANGATTTYFGTPGAEEHAMPMYTRSQALAIRDRIFSELERSSRECDITHDKLNVCIVGGGPTGVEIAGALADFRMQELDILYPEMDPGTLQVTVLQRGDELLKEFSTKYRQYAADELRDRGVVLQLGRGVKEVGYDHVILDDDSVVESDITIWAAGVAIPESVSEWGFPQDKRGRLAVDDYLQVKGFPGVYAAGDIAGQDEPLPQLAQPAIQSGQAAARAIAAEVAGKPRKKFRYLDLGTMATIGRHAAIAEIPVLGGLSGSAGWAAWLGVHVMKMLGHRNQRAVAMNLVSLYGGTRATHQPNPVVGEVDSLRAAKIFEEQAPNRMFGANAGTTGPAAKTAAKDAPGAADVAEPTKD
>NZ_CP023564.1|WP_169928779.1|641126_643604_+|5'-nucleotidase-C-terminal-domain-containing-protein
MLDTPARRIARGASAGLGAAALAVASAVVPVGAAAAEIGDEVTLMTINDFHGALGGASDLACTVETVRQDAQESFLLSAGDNVGGSSFASAVQNDEPTIDVLNALEVDASAIGNHEFDQGQDDLKNRIEGRTDFPDLAANVYNADGTRLMEPYTVIDDGGVKVAVVGAVTTKTVGKVSPAAIEGLDFRDPVDEVNKAIGELEADGVEYDILVASYHEGASANAEPGVAPKNTDPMFDKIVAETDPEVDAIFNGDSHRVYNFNADVPGQDGEVRPVIQTGSSAENLGVVSLALGEDGDWDVVGEPENRPTAQGDAGCAISTPVTEKVDQIAQDAIAEADVIGAQPVGSVATDVTTSWDDTKASYVDGVRTADAPIGNQATTKGDNRTRHSAAGDMLADSMKWYLEDAGLAGDDEVIGFMNPGGIRAELWYDAAGAEGDGVVTYAEANSMVPFGNTLNAGEVTGDQFIQMLEEQWQRTADGGAVDEGDESFLAFSVSNNVEYVFDSTRERDDRIIDVRINGESIDPDATYTIVTASFLFEGGDNMWALSEAHNVRDSGVLDRDAFLQYLQSEDGQNLEPSYAQRQIDLQILDGGEYDSEAGVDRDPVLRIGNVESQSLGAPEIETVQVDAGEYGTFEAPYTLDEETGRLYADVTLTDWMCVPEGTQVPLTITAVPETGTEIVTEIGSFTWTAGGAPDECDTATPPPGDDDDDEPTTPPATEEPTTPAPGDGDDQGDGQGGDDQGQDQGGDDQGEDEAGGPAVIADGNGDDADDPADVIPAEDTTAGGSDRSDLARTGVEVGPMVAAIGVISLAGVAALGLRRRMTRR
>NZ_CP023564.1|WP_169928780.1|643797_646545_+|ExeM/NucH-family-extracellular-endonuclease
MSSTAHGPRLRSRLARVGGATAALALGLSLAPGILPSALAAAVAPGDLQINEVYGGGGNSGAAFQNDFVELVNTSDADISIDGWSLQYASKTGAFNNSLSLTGTVPAGGTFLVQLAAGNGNGDPLPAADLTGGINASGTGGVFALSDAEGKLACTGTTCAEDPAVVDLVGWGGASTFSGEAPAPATTNATSVARTAATGENSTDFAAGAPTPTNAAGEGSGGEGPVDPGDPEEPPADAAEASIAEIQGTGAASPLVGKNVITEGVVTAVYATGGLNGYVIQTGGTGGALDFSTHTGSTAVFVYSSATAGQVAIGDSVRVTGEVAEYNGSTQITVGASGLEKLEQPLEPVEPATLEGGFPTEESQRESLEHMLYLPGEGDFTVTDIYSTNKYGEITLAIGDEPLQQAGDIMAPGAEATEYFESRESLKVLLDDGRTTNFQSTPTSPMSWLTTEEPVRVGAAATFTEPVVVAYSFDQWRLNTTTPWTSSDSDGVDFEDTRQDAPDEVGGDVKLSTFNVLNYFTTLGEDTPGCEPYTNMNGEGTNVRGGCDLRGAWGADDLERQQSKIVDAISGTGADVVGLTEIENSARIDGDPDEATATLVAALNEKDGAGTWDYIPTDPAYQALGLTGGQDAITNAIIYKPAEVAPQGEAQILAGDPAFDNAREPIGQAFVPLEGSGEEQVQGEPFFFSINHFKSKGSADAEDSGLPADPVQGNSRTSRLQQAEALLAWSEETAAGLGVEDVYLGGDFNAYTQEEPLQIFYDEGFVNLAETHDPGSWSYSYGGMVGSLDHVIANPSGAERVTGATDWQINGAESVMTQYARYQNNITDLYESGPFGSSDHDPIVVGLAGGFSEEEPGNGGDNGSGNGNGNGNGNGNGNGNGPRENDNRGPGKNNGTPGGSNSGIGHGAGGKGGKG
>NZ_CP023564.1|WP_096798298.1|646630_647995_+|APC-family-permease
MTSTSGALARRLGLRDAVVIGLASMIGAGAFVSLGAASDLAGALAPLAVLLAAGVALCNATSTAQLAAQHPASGGTYHYGREQLGPWWGFLAGWCFVLGKIASCAAMALVIAAYLVPEPAQRIVAALVVVVLTGVNLVGVTRTAALARVLVSVALVALVLTGARLVGGVLLGAGGSAGSDAADAGAAIPGPLAGSAAGLWDGGLAAVLGAGAGGAAGIVLAVAQAAALMFFAFAGYARVATLGEEVVEPRRTIPRAILLALAVVAALYLALSVVLVLVGPAPGADGWGPAPFLTALDAVGAGGAWHAVITVGAVAAATGALLALVAGISRTALAMARERDLPPVLAPVSPRFSVPQRAELAAGIAVVLLVLLASDVLVAIAASSFGVLLYYAIANLAALTQVGQWRLFPKAMQVIGLVGCLLLVAALPGRTIVAGAALVLAGVAYRGVVLAVRR

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Crispr_ID: NZ_CP023564_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP023564_4

3810790-3810957

Orphan

Consensus_repeat	Method
ACAGCAGCCCTCAACGGTCAGCTGGCGAACCGGAATCGCGCCGGATCTGGTTCG	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP023564_4

>merge|NZ_CP023564|4|3810790-3810957|CRISPRCasFinder
ACAGCAGCCCTCAACGGTCAGCTGGCGAACCGGAATCGCGCCGGATCTGGTTCGCCAGCTGACAATCGGCACGCCCGGCCCGGCGAACCGCGGTGTCACCACCACCACGCGGCCACAGCAGCGCTCAACGGTCAGCTGGCGAACCGGAATCGCGCCGGATCTGGTTCG

>NZ_CP023564|4|3|3810790-3810957|CRISPRCasFinder
ACAGCAGCCCTCAACGGTCAGCTGGCGAACCGGAATCGCGCCGGATCTGGTTCG	CCAGCTGACAATCGGCACGCCCGGCCCGGCGAACCGCGGTGTCACCACCACCACGCGGCC
ACAGCAGCGCTCAACGGTCAGCTGGCGAACCGGAATCGCGCCGGATCTGGTTCG

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP023564.1\|WP_096800750.1\|3819227_3819941_-\|FadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225097
NZ_CP023564.1\|WP_096801162.1\|3800743_3801868_+\|Gfo/Idh/MocA-family-oxidoreductase	unknown	unknown	gnl\|CDD\|223745
NZ_CP023564.1\|WP_096800744.1\|3811007_3811946_-\|amidohydrolase-family-protein	unknown	unknown	gnl\|CDD\|226145
NZ_CP023564.1\|WP_096800747.1\|3813294_3814689_-\|fuconate-dehydratase	unknown	unknown	gnl\|CDD\|239440
NZ_CP023564.1\|WP_096800739.1\|3803743_3805414_-\|ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|173871
NZ_CP023564.1\|WP_096800738.1\|3802109_3803744_-\|ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|224048
NZ_CP023564.1\|WP_096800741.1\|3806453_3807395_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|224094
NZ_CP023564.1\|WP_096800746.1\|3812927_3813266_-\|L-rhamnose-mutarotase	unknown	unknown	gnl\|CDD\|377501
NZ_CP023564.1\|WP_096800751.1\|3820019_3820934_-\|NAD(P)-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224995
NZ_CP023564.1\|WP_096800749.1\|3817296_3819015_-\|dihydroxy-acid-dehydratase	unknown	unknown	gnl\|CDD\|235708
NZ_CP023564.1\|WP_096801163.1\|3810066_3810759_+\|FadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|225097
NZ_CP023564.1\|WP_096800745.1\|3811932_3812931_-\|aldo/keto-reductase	unknown	unknown	gnl\|CDD\|381378
NZ_CP023564.1\|WP_096800737.1\|3799830_3800712_+\|sugar-phosphate-isomerase/epimerase	unknown	unknown	gnl\|CDD\|224007
NZ_CP023564.1\|WP_096800736.1\|3798821_3799781_+\|TIM-barrel-protein	unknown	unknown	gnl\|CDD\|275172
NZ_CP023564.1\|WP_096800742.1\|3807847_3808741_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP023564.1\|WP_096801164.1\|3815994_3817287_+\|L-fucose:H+-symporter-permease	unknown	unknown	gnl\|CDD\|340952
NZ_CP023564.1\|WP_096800752.1\|3821136_3822105_-\|C-terminal-binding-protein	unknown	unknown	gnl\|CDD\|240624
NZ_CP023564.1\|WP_169928859.1\|3814766_3815621_-\|fumarylacetoacetate-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|223257
NZ_CP023564.1\|WP_096800743.1\|3808799_3810029_+\|toxic-anion-resistance-protein	unknown	unknown	gnl\|CDD\|377557
NZ_CP023564.1\|WP_096800740.1\|3805410_3806457_-\|ABC-transporter-permease	unknown	unknown	gnl\|CDD\|223674

Protein	Function_ID	Function_description	E-value
NZ_CP023564.1\|WP_096800750.1\|3819227_3819941_-\|FadR-family-transcriptional-regulator	gnl\|CDD\|225097	COG2186, FadR, Transcriptional regulators [Transcription].	1.18839e-34
NZ_CP023564.1\|WP_096801162.1\|3800743_3801868_+\|Gfo/Idh/MocA-family-oxidoreductase	gnl\|CDD\|223745	COG0673, MviM, Predicted dehydrogenases and related proteins [General function prediction only].	5.60539e-56
NZ_CP023564.1\|WP_096800744.1\|3811007_3811946_-\|amidohydrolase-family-protein	gnl\|CDD\|226145	COG3618, COG3618, Predicted metal-dependent hydrolase of the TIM-barrel fold [General function prediction only].	1.25009e-38
NZ_CP023564.1\|WP_096800747.1\|3813294_3814689_-\|fuconate-dehydratase	gnl\|CDD\|239440	cd03324, rTSbeta_L-fuconate_dehydratase, Human rTS beta is encoded by the rTS gene which, through alternative RNA splicing, also encodes rTS alpha whose mRNA is complementary to thymidylate synthase mRNA. rTS beta expression is associated with the production of small molecules that appear to mediate the down-regulation of thymidylate synthase protein by a novel intercellular signaling mechanism. A member of this family, from Xanthomonas, has been characterized to be a L-fuconate dehydratase. rTS beta belongs to the enolase superfamily of enzymes, characterized by the presence of an enolate anion intermediate which is generated by abstraction of the alpha-proton of the carboxylate substrate by an active site residue and is stabilized by coordination to the essential Mg2+ ion.	0
NZ_CP023564.1\|WP_096800739.1\|3803743_3805414_-\|ABC-transporter-substrate-binding-protein	gnl\|CDD\|173871	cd08506, PBP2_clavulanate_OppA2, The substrate-binding domain of an oligopeptide binding protein (OppA2) from the biosynthesis pathway of the beta-lactamase inhibitor clavulanic acid contains the type 2 periplasmic binding fold. Clavulanic acid (CA), a clinically important beta-lactamase inhibitor, is one of a family of clavams produced as secondary metabolites by fermentation of Streptomyces clavuligeru. The biosynthesis of CA proceeds via multiple steps from the precursors, glyceraldehyde-3-phosphate and arginine. CA possesses a characteristic (3R,5R) stereochemistry essential for reaction with penicillin-binding proteins and beta-lactamases. Two genes (oppA1 and oppA2) in the clavulanic acid gene cluster encode oligopeptide-binding proteins that are required for CA biosynthesis. OppA1/2 is involved in the binding and transport of peptides across the cell membrane of Streptomyces clavuligerus. 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 from ionotropic glutamate receptors, LysR-type transcriptional regulators, and unorthodox sensor proteins involved in signal transduction.	4.75416e-166
NZ_CP023564.1\|WP_096800738.1\|3802109_3803744_-\|ABC-transporter-ATP-binding-protein	gnl\|CDD\|224048	COG1123, COG1123, ATPase components of various ABC-type transport systems, contain duplicated ATPase [General function prediction only].	0
NZ_CP023564.1\|WP_096800741.1\|3806453_3807395_-\|ABC-transporter-permease	gnl\|CDD\|224094	COG1173, DppC, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	4.69702e-68
NZ_CP023564.1\|WP_096800746.1\|3812927_3813266_-\|L-rhamnose-mutarotase	gnl\|CDD\|377501	pfam05336, rhaM, L-rhamnose mutarotase. This family contains L-rhamnose mutarotase which is a glycosyl hydrolase that converts the monosaccharide L-rhamnopyranose from the alpha to the beta stereoisomer. In Escherichia coli this enzyme is the product of the rhaM gene (also known as yiiL). The tertiary structure has been solved, in complex with L-rhamnose, and the catalytic mechanism determined. His22 is the proton donor. The enzyme naturally exists as a dimer.	2.68799e-21
NZ_CP023564.1\|WP_096800751.1\|3820019_3820934_-\|NAD(P)-dependent-oxidoreductase	gnl\|CDD\|224995	COG2084, MmsB, 3-hydroxyisobutyrate dehydrogenase and related beta-hydroxyacid dehydrogenases [Lipid metabolism].	6.78661e-76
NZ_CP023564.1\|WP_096800749.1\|3817296_3819015_-\|dihydroxy-acid-dehydratase	gnl\|CDD\|235708	PRK06131, PRK06131, dihydroxy-acid dehydratase; Validated.	0
NZ_CP023564.1\|WP_096800745.1\|3811932_3812931_-\|aldo/keto-reductase	gnl\|CDD\|381378	cd19152, AKR_AKR15A, AKR15A family of aldo-keto reductase. The AKR15 family includes Microbacterium luteolum pyridoxal 4-dehydrogenase (PLD), Pseudomonas sp. D-threo-aldose 1-dehydrogenase (FDH), and similar proteins. PLD (EC1.1.1.107) catalyzes irreversible oxidation of pyridoxal. FDH(EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose. FDH (EC1.1.1.122), also called (2S,3R)-aldose dehydrogenase, or L-fucose dehydrogenase, catalyzes the oxidation of L-fucose to L-fuconolactone in the presence of NADP(+). It is also active against L-galactose, and to a much lesser degree, D-arabinose.	5.27918e-114
NZ_CP023564.1\|WP_096800737.1\|3799830_3800712_+\|sugar-phosphate-isomerase/epimerase	gnl\|CDD\|224007	COG1082, IolE, Sugar phosphate isomerases/epimerases [Carbohydrate transport and metabolism].	2.00209e-37
NZ_CP023564.1\|WP_096800736.1\|3798821_3799781_+\|TIM-barrel-protein	gnl\|CDD\|275172	TIGR04379, myo-inositol_catabolism_protein, myo-inosose-2 dehydratase. Members of this family include the enzyme myo-inosose-2 dehydratase, product of the gene iolE, as found in inositol utilization cassettes in many species. [Energy metabolism, Sugars].	3.01326e-52
NZ_CP023564.1\|WP_096801163.1\|3810066_3810759_+\|FadR-family-transcriptional-regulator	gnl\|CDD\|225097	COG2186, FadR, Transcriptional regulators [Transcription].	1.26254e-49
NZ_CP023564.1\|WP_096801164.1\|3815994_3817287_+\|L-fucose:H+-symporter-permease	gnl\|CDD\|340952	cd17394, MFS_FucP_like, Fucose permease and similar proteins of the Major Facilitator Superfamily of transporters. This subfamily is composed of L-fucose permease (also called L-fucose-proton symporter) and similar proteins such as glucose/galactose transporter and N-acetyl glucosamine transporter NagP. L-fucose permease facilitates the uptake of L-fucose across the boundary membrane with the concomitant transport of protons into the cell; it can also transport L-galactose and D-arabinose. Glucose/galactose transporter functions in the uptake of of glucose and galactose. The FucP-like subfamily belongs to the bacterial fucose permease, eukaryotic Major facilitator superfamily domain-containing protein 4 (FucP/MFSD4) family of the Major Facilitator Superfamily (MFS) of transporters. MFS proteins are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.	5.57085e-128
NZ_CP023564.1\|WP_096800752.1\|3821136_3822105_-\|C-terminal-binding-protein	gnl\|CDD\|240624	cd05299, CtBP_dh, C-terminal binding protein (CtBP), D-isomer-specific 2-hydroxyacid dehydrogenases related repressor. The transcriptional corepressor CtBP is a dehydrogenase with sequence and structural similarity to the d2-hydroxyacid dehydrogenase family. CtBP was initially identified as a protein that bound the PXDLS sequence at the adenovirus E1A C terminus, causing the loss of CR-1-mediated transactivation. CtBP binds NAD(H) within a deep cleft, undergoes a conformational change upon NAD binding, and has NAD-dependent dehydrogenase activity.	1.79684e-147
NZ_CP023564.1\|WP_169928859.1\|3814766_3815621_-\|fumarylacetoacetate-hydrolase-family-protein	gnl\|CDD\|223257	COG0179, MhpD, 2-keto-4-pentenoate hydratase/2-oxohepta-3-ene-1,7-dioic acid hydratase (catechol pathway) [Secondary metabolites biosynthesis, transport, and catabolism].	2.9507e-81
NZ_CP023564.1\|WP_096800743.1\|3808799_3810029_+\|toxic-anion-resistance-protein	gnl\|CDD\|377557	pfam05816, TelA, Toxic anion resistance protein (TelA). This family consists of several prokaryotic TelA like proteins. TelA and KlA are associated with tellurite resistance and plasmid fertility inhibition.	8.0692e-56
NZ_CP023564.1\|WP_096800740.1\|3805410_3806457_-\|ABC-transporter-permease	gnl\|CDD\|223674	COG0601, DppB, ABC-type dipeptide/oligopeptide/nickel transport systems, permease components [Amino acid transport and metabolism / Inorganic ion transport and metabolism].	2.31044e-93

>NZ_CP023564.1|WP_096801163.1|3810066_3810759_+|FadR-family-transcriptional-regulator
MASAVTDRAIGAIKQMVIDGTLKPGDRLPTESELSERIGVSRNSLREAVKALSVIRVLDVRQGDGTYVTALEPEQLLESLAFVLDLHQDSSYVEIIEIRRLLEPVAVEQACPHLVDEDFVRLEQTMADLDGSSTIEELVEADIAFHHLINDRCPNDYLSSLLDSLASSTSRARVWRGLTDDSAVERTLSEHRRILDALRAGRADLARTYAAAHVAGVESWLLQKGEPPVS
>NZ_CP023564.1|WP_096800743.1|3808799_3810029_+|toxic-anion-resistance-protein
MDKLQPPAPAQEITPAEPVASVDDDQAGAMLPDVPAEQQAELEQRADSWVEQVAQLNPHSQEYTAQVNALGAVARRTFERTTQTSSRFMQQSLRESKEKGTAQESVAKSLSELRTTMEDLAPKEETFGSKALGWLPGRNVAKRYFRTFESNQDQLDQVLGALGRGQEMLQKDNAELAVERRALWEDLAALKKASYLLGLLDDRAVRRAEQTRAEGRAAEADALERDVLFAVRQRRQDVATQIAVTVQAYLSMGLIEDNNTKLQQGVERARTTTVTALRTAVITAQALENQKIVLDQIDAVNRTTDNLISRTSQMLADNSVKIQEQAATSGVSEETLQKAFDNLFTTMDGIDAFRSQANQNFLTTVTNLERQVERSQPYLERMQKEQPEHEQIEQASANAMDLLEIEDPR
>NZ_CP023564.1|WP_096800742.1|3807847_3808741_+|hypothetical-protein
MSAAQDPSAEPPTNGDSRFPDPFAPSPGDQDLPWKATAERRDLWGPVQKPLEGTVSSPASRAVGRPRRSPLVRFGAPVVVGGLAALITLAVVLGTGLGGPLLAVAAAAGVGVVALGGVGVAANLPRREQERPVLDASVAGGTRELLERILTADVTTRERLAPLRPQATSTPAAVTVLDAVGTLTTRIDALVGSERLQAQRASSSEVMMLEGIACRYVPELVDAAGETIGFLRTFEGTARQEAMANLESIDRQLDVLREEVEQIEGDIVGGVSRSLEVHAEFLRTRFADHHLDPIIDV
>NZ_CP023564.1|WP_096800741.1|3806453_3807395_-|ABC-transporter-permease
MMTSSEALPAEAAASHEERPARPGVGRAFLRPLPLAAAVVVVLSVLGALLAPQLAALSGNDPFTYHSDALAADTSPAGAFGGVSGAHWFGVEPGTGRDLFSLVLYGARVSLLVGLASTVLATLIGVVLGIVAGAVGGLVEKLVDFATDVTLGFPFLIFAIALSALFPLEAPRALLLTLVIGMFGWPGIARVVAAETRVIVQQPYVVASRVMGARFGHLFRHQVLPNVASTVIVYSCISLPGRIAAEATLSFLGVGMLPPTPSWGRSIGDAIGWLLVDPAFLLFPAAALFLVTFSFNILGDTLRDALDPRGGRA
>NZ_CP023564.1|WP_096800740.1|3805410_3806457_-|ABC-transporter-permease
MNPAVLRAVRSLGVLLAVLVLTYAIFYMAPVDPALRMCGKPCSPEDLEAARGFMGFDTPWWAQLGSFLAAIFVGRTFGSADVVVECAAPCLGYSFQYHQDVTSLIIERFPVTLSIALGAVALQVILGVAAGALSARRQGGLLDRVVTGISVVAASAPAFVVGLLAVVVFALRLDLLPSGGYENFADGPLEWARHLVLPWATLAFLNGAVYARLVRSSMIEQLGLDYARTARAAGLSERRIDRYALRNLALPLTTLVALDIGALLGGAVITERIFGLPGLGALLLDATATADLPVIVGTTFLGSLLIVLANLSADLARPLLDRRLAVGGRRPATPTATTPTTTTQENPS
>NZ_CP023564.1|WP_096800739.1|3803743_3805414_-|ABC-transporter-substrate-binding-protein
MNSPRLPRRGLLAAGPVLLGLGALAACSNDSSGSSDAGGGESGGTLTIFTSSEEISFDPATSQNLAITTLGLIARRLTAWKTSADAPTELIPDLATDTGTPSDDGKTWTFTLQEGLLFEDGTPITAATVKYGLERSFASELTGGLTYHKVLLEGGEDYEGPFSGKHLDSIEAADETTLVFHLNRPYGDFGWIASTPAFAPVPEDSGEPEKYATAPIASGPYRLKSYSAGSQAVMERNEKWDGATDAARTGGPDTIEFALAQDPSVVAQSLIADRSDAQDAFLASFVPTAQLVQAQNDPKVGDRLVTSGPGALEYLALNTSSKALEDVKVRTAIQYAVDKEAYRTAKGGEISGDYATTLITPGIAGREEYSLYGDEPAGDPEKAKTLLAEAGASDLSLRLLITEDDTASAEAIQQGLARAGITVTIQPLDQNAYDSEVTAGDGTGYDLVLSSWQPDVPSPNANLTPLFDSSQIGNGNYNLARYDNPDVDKAILEASSTLDADEAHAKWAAVDKQILEDSPVVPLIYSKNSFLHGSGVENFVIGEFPAYPNYLTVTLG
>NZ_CP023564.1|WP_096800738.1|3802109_3803744_-|ABC-transporter-ATP-binding-protein
MSTADELLALRGLQVGIAGRSIVTGLDLTVRRGRITALVGESGSGKSITALSTIGLQPPGAEVGGSAVLEGEELVGRSATQLRRIRARRVGTVFQEPGQSLSPVMKVSAVFRDVLAVREDLRGKARVQARTTELLRSVGLPDPDRTAASYPHELSGGELQRVVIALALSGGPDLLIADEPTTALDVTVQRGILELLRRIVDEGEVGILLITHDMGVVGEIADDVVVLRDGEVQETGPVREVLTAPASEYTQELLRAVPRLDEALAGEMGATADGAGADEAPVVRIEGLSVEYQRRGGGHRALDDVSMEVRRGEIHGLVGESGSGKSTWGKALAGLVPTEARLLELDGVDPRSLPRAERRAAYSRVGMVFQNPASSLNPRRTVGWSIGEPLQLAGDVNRLDTARRVREALELVRLPASYSTRLPHELSGGQRQRVSIARALIRRPSLLIADEPTSALDVTIQAHVIEVLRDAIEEARFACVFISHDLAVVGSLADHVTMLRAGRTVEQGPTRSVLGDPQHEYTRTLLASIPNPERRLREGGPTAA
>NZ_CP023564.1|WP_096801162.1|3800743_3801868_+|Gfo/Idh/MocA-family-oxidoreductase
MGRLHASSYQRLPSRYPDLGIRPRLVVAADPLEENQRAAVEQFGFGRAVASIDEVLADPEVDVVSICSPNFLHRDFAIQAAEAGKPFWIEKPMGVSAEQSREIHDAARSAGVATAVGFNYRHAPAVAHLRSMIAGGRLGRITNVRCWLDADYASSPDGPLTWRYDRARGGSGVIGDLLSHGVDLVQHVTGQRLAEVTATSDVFIPERPLPLGAGVGHGAVAVSEERGPVENEDWVAALGRLDGGAHATLESSRVARGHRSDYALEVFGTEGSARWSFTRMNEFEVMIGDGGTEHGYTTVLAAAGHGDYARFQPGPGIPMSFDDLKTIEAAAFLSDAAHGTHLAPTAADGLAAAEACEAIVRSAASRAWEAVPQG
>NZ_CP023564.1|WP_096800737.1|3799830_3800712_+|sugar-phosphate-isomerase/epimerase
MVKILLDPSMYHPHLSVAEELHKARELGFDHLELSPRADFHEWHHYPKVDRHLIAEVTQAMKDTGVSIGSLNPVFDWASPDEQERQAQVRNWRRLLEIADALEVPLIATEFSGDPNRARQSEAQFYRSMEELIPHFEKYGLECTIEAHPYDFVEENDRAVQVIRGVDRDWLNYEFCFPHAFHLGQGARDVREMMDYAGDRLKHLHIADVFDHTANVGNRYIMNPPGVDARIHQHNEIGNGEIDWDASFAYLREREYDGTVSVCVFGWEEEADAINVRMLERIEKELGQGGSRA
>NZ_CP023564.1|WP_096800736.1|3798821_3799781_+|TIM-barrel-protein
MTTTSDSAAGRTDRSRNPEAPFDKLTVGVCPDQWGVWFPEDEKQIPWRTALGEMAEAGFSVMETGPWGYFPKDAKELRSVMDEHGFQVVAGTGWGILHKEEAWAETERTFRAIAETHAAVGAEYMVHLPPMYRDEKTWQFTDDRELTGEAWKRYVTNANELGRIMKEDYGLTMVLHPHGDSHIETPEEISRVFEATDPELVSFCLDTGHIVYGGGDPVQMIEQYPERIGYVHIKAFDPDITREAHEKDWPFGEAVAKGASVRPPAGLPDMKELVAKLATLDKELYVICEQDLYPCEPGLPLPNAIATRVFLAECGLGVK
>NZ_CP023564.1|WP_096800744.1|3811007_3811946_-|amidohydrolase-family-protein
MPGADPSADGVVGGADGAGAAGAVTDTHLHLWDLAESSYAWLAGAAEPLRRTVSFEGVRADLEQLGVTRVVLVQADDTTADTAHLQRAARAIEAGPDGGASTVVRADVVGWLPLMDPAAVREALADPQRTDHLVGVRHLVHDEPDPGFLDRPEVAQSLDLLAEAGPPLDVPDAFPRHMEQVECVARRHPGLTVVLDHLGKPPLGDAAAMPLWDAQLERIAACPNVVAKVSGLATSGDGDFAAAADRALELFGADRLMVGSDWPIAPTHLDLGSGFAPLLAHVRTWEAADVAAVTRGTAARIYRRPGDPAPAT
>NZ_CP023564.1|WP_096800745.1|3811932_3812931_-|aldo/keto-reductase
MSARQPLALPRLGFGAAQLGNIFRVTTDEEADGAVRAAWDAGIRYFDTAPHYGVGTSERRLGERLAGYPRDEYLVSTKVGRLLVPGPGTGDDLENGFHVPDDLVRRWDWTEAGVRRSHAESLERLGLDRVDILFAHDPEEGPADAAIEEGLPALAAMREEGLVSAVGVGSKDADVLTRAVRTGLIDLVMLSGRYTLLEQAASAELLEACIEHGVGVVAVSVFNSGLLSRHQVAEDSHYEYAQAPAELIARARELAAIAERHGVTLPDLAVQYPLRHPAVRSVALGMRTAAQVESNAERMGVEIPEVAWEDVARLEAAARQGSATGESPDAGR
>NZ_CP023564.1|WP_096800746.1|3812927_3813266_-|L-rhamnose-mutarotase
MENIALHTRIAEGREADYDREHARIPDELDASLRAAGVHAWRIWRDGRDIFHLVEVEDYQAMRRTLAQDPVNQRWQEHINQYLEVVDDYGGEDTGIRPVWELPEQPAAGVSA
>NZ_CP023564.1|WP_096800747.1|3813294_3814689_-|fuconate-dehydratase
MSIFTALDVQDVRFPTSRDLDGSDAMNTDPDYSAAYLTVRTDTPDEGTALVFTIGRGNDVQSAAIAALAPHLVGRDVEEVLADLGGMYRELTHDSQLRWLGPDKGVMTMAIGAVVNALWDLRARREGRPLWLTLASLGPEELLDLVDLRYLEDALTREEALEILRRGAEGKEERIAALREHGVPAYTTTPGWLGYSDEKLTRLLGEARDEGFEMVKLKVGADPADDERRMRIAREVMGPGFPIAIDANQRWGTAEAIEAIRALAPYEPYWVEEPTSPDDILAHAAIRQGVSPVRVATGEQGASRVLFKQLLQAGSIDVLQADATRVAGINENLAILLLAAKFDIPVCPHAGGVGLCEMVQHVAFLDAVAVGGEDQRRRIEFVDHLHEHFEVPVRIENGAYMPPEEVGGGARMHAASVQDHLFPDGPVWAEGAEGVASASSDLSDPSAAGTPGAAPVAPSAAVAP
>NZ_CP023564.1|WP_169928859.1|3814766_3815621_-|fumarylacetoacetate-hydrolase-family-protein
MELRRLGPVGQEKPAVVSEGATYRLDGLTADIDGGFLAADGIARVREALAAGDLPVWEGADAERIGAPIARPQAVLCIGQNYAAHAAESGAEPPAVPILFHKHPNTVVGPEDDVEIPPGAQKVDWEVELGVVIGMEAAYLPDEQAALGVIAGYVTSHDVSERGYQLAESGGQWSKGKNARGFNPLGPGLVPADEIDPQTLRLASSVNGEPRQDSTTADMIFSVAQIIQHLSQFMVLSPGDLINTGTPQGVALSGRFPYLVAGDVVEIGIENLGAQRTTFVPATI
>NZ_CP023564.1|WP_096801164.1|3815994_3817287_+|L-fucose:H+-symporter-permease
MRLPFILIVTCFAAWGVLNNMTDPLVSVFSSVFSMGAFQSSLVQFAFYGAYCVLAIPAAWINSRPGYKGGVLIGLLLASFGGFLFFPASQIMTYTMFLAALFTLAAGLSILETSANPYVMAMGPEATATRRLNVAQAFNPVGSNLGVLLAAMLILPRVNPSTAEERAALSQDELESIRSSELQAVMGPYIGVAMALVLIAIAIAMVRVPKNPAVMADAERGAEQRIGARLSRLLRNRRYSFGVVAQFFNIAAQICIWTFTIHYVTETLGVDDTRAGYWLQASLLVFLIMRFVMVALMGRFDARKLMVLMCTLGTALSVLAVLSGNIVGAVAIVLLSGCISLLFPTIYGVALEGLGQDTKYGAAGLIMAIVGGAVMPLLHGWVIDISSARTSYLVVAVCFAVVAAYGIYVLRTPSPAAAESEAEAGADTAA
>NZ_CP023564.1|WP_096800749.1|3817296_3819015_-|dihydroxy-acid-dehydratase
MNELRSADWYVGDDRNAYIHRAWMRRGLPASAFDGTRPHIAIANTASALVPCNMHLGEVARSVSDGIYEAGGIPLELPVMGLGETLVRPTAMLWRNLAAMQMEEMFRANPLDAVVLLGGCDKTVPALLMAAASVGLPALVVPGGPMLSGTFRGTPLGCGTDVWKLSEDVRGGDLTEKDFLASESSMIRSKGHCNTMGTASTMGLVAEALGMVLPGLAGTPAPDARLLEGAHASGRRIVEMVAEGLTPQKVITEGSVRNAIVALAAIGGSTNAVVHLLAIAGRLGLDISIDDFDRTGADVPLLVNLQPSGKHLMDDLFRAGGFLAVLREVRELLDPEAITVSGRPLADHLDEARIWDADVISARETPLQEKAGIAVLRGSLAPEGAIVKPAAATPALLQHRGPALVFDSIEDFRSRIDDPELEVDEDTVLILRGCGPKGYPGMPEVANMPLPRKLLERGVRDMVRICDGRMSGTAYGTVVLHVSPEAADGGPLAQVRTGDTIVLDVEQRRLDVEVDPAELAARTPDAATVEGFATPARGWQRLYIDHVTSASLGADLDVLTGASGPDVHRESH
>NZ_CP023564.1|WP_096800750.1|3819227_3819941_-|FadR-family-transcriptional-regulator
MPAPVLHSEVARALGEEIVGGVVPAGHVLTLAGLEERFSRSRTVLREAVRVLESLGLVVSKRRVGVVVQPPEAWSVLSPQVIAWRLGSGAREEQLRSLTQLRRAIEPNAARAAAARRGGDAAGPLLEAAERLQALGERGEGATEAYIEADVAFHAQLLRASGNEMFAALEPSISEVLRGRARLGRNPAWPTPRSLDHHRELARAVAEGRAEEAEAMARAIAGDVLREVAGHEGSPED
>NZ_CP023564.1|WP_096800751.1|3820019_3820934_-|NAD(P)-dependent-oxidoreductase
MPSHESAVPPPGTSAADPGAPTVSVLGLGPMGAPIARNLLASGRPTTVWNRTRSRAEAFAADGARVATTVADAAADVVLAVLPDVPQLREILDEAALAAFEAAGSLLVITSTTSPEQVRALAEELAPRGVRVLDAPMSGGVAGAVAGTLSLMVGGAEEDVARARPVLETIGGTLTHLGPLGAGSLAKLCNQVVVAGTLAALAEAYGLARAGGIDAEGLTEVLAGGLAASEVLTQKRDKLLERDYALGGSTDNQVKDLRYATAALEQAGVTGRLTPVLLAAYTEVVERGGGQLDHAAVQELYLDE
>NZ_CP023564.1|WP_096800752.1|3821136_3822105_-|C-terminal-binding-protein
MKIAIVDSDNESFEEEHKVAERFGIELSRSQASDEQQTIEAARGADAILVQYAPITAAVLDALPDLRAIGRYGVGVDTVDVEAATARGIAVCNVPDYGVQDVSDHAIALTLSVVRGTARLDRLVRAGEYGLVPVKPLHRISTLRFGVVGLGRIGAATARKAQALGFTVIGSDPQLEIGSRTADDIEVVDFEILLSTCDVISLHVPLLESTRHLIGEETLARMKPGAMLINTCRGGVVDTEAVARALQDGRLQGAGLDVFEQEPLGLDSPLMDCPGAVLTPHASWYSEESYSELKRRVTEAVAAVIRGERPRDILNPEVLDRA

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity
NZ_CP023564_1	1.1\|126160\|21\|NZ_CP023564\|CRISPRCasFinder	126160-126180	21	NZ_CP023564.1	1999864-1999884	2	0.905
NZ_CP023564_1	1.1\|126160\|21\|NZ_CP023564\|CRISPRCasFinder	126160-126180	21	NZ_CP023564.1	3489200-3489220	2	0.905

1. spacer 1.1|126160|21|NZ_CP023564|CRISPRCasFinder matches to position: 1999864-1999884, mismatch: 2, identity: 0.905

ggatcacgaccacgagggcca	CRISPR spacer
ggatcacgaccaccacggcca	Protospacer
************* * *****

2. spacer 1.1|126160|21|NZ_CP023564|CRISPRCasFinder matches to position: 3489200-3489220, mismatch: 2, identity: 0.905

ggatcacgaccacgagggcca	CRISPR spacer
ggatgacgaccacgagggtca	Protospacer
**** *************.**

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_CP023564_2	2.1\|592125\|30\|NZ_CP023564\|CRT	592125-592154	30	NZ_CP013105	Paraburkholderia caribensis strain MWAP64 plasmid 2, complete sequence	208409-208438	6	0.8
NZ_CP023564_2	2.9\|592593\|30\|NZ_CP023564\|CRT	592593-592622	30	NZ_CP017944	Phyllobacterium zundukense strain Tri-48 plasmid unnamed4, complete sequence	129432-129461	6	0.8
NZ_CP023564_2	2.2\|592173\|30\|NZ_CP023564\|CRT	592173-592202	30	NZ_CP018784	Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence	315235-315264	7	0.767

1. spacer 2.1|592125|30|NZ_CP023564|CRT matches to NZ_CP013105 (Paraburkholderia caribensis strain MWAP64 plasmid 2, complete sequence) position: , mismatch: 6, identity: 0.8

cgaggtcaacaccgctgagaacacggacgt	CRISPR spacer
cgaggtcaacgccgctgagatcatcgagtt	Protospacer
**********.********* **. **  *

2. spacer 2.9|592593|30|NZ_CP023564|CRT matches to NZ_CP017944 (Phyllobacterium zundukense strain Tri-48 plasmid unnamed4, complete sequence) position: , mismatch: 6, identity: 0.8

ggcggacaacgctgccgagaacacggatgt	CRISPR spacer
gtcggccaatgctgccgagaacacggtctt	Protospacer
* *** ***.**************** . *

3. spacer 2.2|592173|30|NZ_CP023564|CRT matches to NZ_CP018784 (Curtobacterium pusillum strain AA3 plasmid pCPAA3, complete sequence) position: , mismatch: 7, identity: 0.767

ggcggacaacgctgctgagaacac-cgacgt	CRISPR spacer
ctgggacaacgatgctgagaacacgcagcg-	Protospacer
   ******** ************ *..**

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site	Prophage annotation

Anti-CRISPR protein detection

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