NZ_CP047186_1
1984331-1984417
Orphan
NA
Consensus_repeat
Method
GCTGGCGAAGGGGTTGTTGCCGGGGCG
CRISPRCasFinder
1 spacers
>1.1|1984358|33|NZ_CP047186|CRISPRCasFinder
CGGGGCGGCCGGACGCTGACCCATGCCCTGGTT
Detail
CRISPR arrays
Neighbor Proteins Overview
HMMScan for Signature genes
rpsblast for functional proteins
Protein sequences
The CRISPR arrays of NZ_CP047186_1
>merge|NZ_CP047186|1|1984331-1984417|CRISPRCasFinder
GCTGGCGAAGGGGTTGTTGCCGGGGCGCGGGGCGGCCGGACGCTGACCCATGCCCTGGTTGCTGGCGAAGGGGTTGTTCCCGGGGCG
>NZ_CP047186|1|1|1984331-1984417|CRISPRCasFinder
GCTGGCGAAGGGGTTGTTGCCGGGGCG CGGGGCGGCCGGACGCTGACCCATGCCCTGGTT
GCTGGCGAAGGGGTTGTTCCCGGGGCG
Protein
Signature genes
Signature genes Name
Protein_function
NZ_CP047186.1|WP_068208365.1|1990534_1991704_-|flavodoxin-dependent-(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase
unknown
unknown
gnl|CDD|234737
NZ_CP047186.1|WP_132504128.1|1978489_1979089_-|hypothetical-protein
unknown
unknown
gnl|CDD|180660
NZ_CP047186.1|WP_082844959.1|1985108_1985411_-|YlxR-family-protein
unknown
unknown
gnl|CDD|377288
NZ_CP047186.1|WP_132504407.1|1991971_1993339_-|site-2-protease-family-protein
unknown
unknown
gnl|CDD|100084
NZ_CP047186.1|WP_068212047.1|1975983_1976352_-|hypothetical-protein
unknown
unknown
unknown
NZ_CP047186.1|WP_068212051.1|1974473_1975415_-|bifunctional-riboflavin-kinase/FAD-synthetase
unknown
unknown
gnl|CDD|235536
NZ_CP047186.1|WP_068212045.1|1977412_1978411_+|ketopantoate-reductase-family-protein
unknown
unknown
gnl|CDD|235821
NZ_CP047186.1|WP_068212053.1|1972838_1974386_-|SDR-family-oxidoreductase
unknown
unknown
gnl|CDD|187556
NZ_CP047186.1|WP_068213513.1|1981464_1981896_-|30S-ribosome-binding-factor-RbfA
unknown
unknown
gnl|CDD|234787
NZ_CP047186.1|WP_068208356.1|1985462_1986464_-|transcription-termination/antitermination-protein-NusA
unknown
unknown
gnl|CDD|237061
NZ_CP047186.1|WP_068212049.1|1975414_1975933_-|hypothetical-protein
unknown
unknown
unknown
NZ_CP047186.1|WP_068208362.1|1990030_1990513_-|hypothetical-protein
unknown
unknown
unknown
NZ_CP047186.1|WP_068208368.1|1993418_1994501_-|1-deoxy-D-xylulose-5-phosphate-reductoisomerase
unknown
unknown
gnl|CDD|235472
NZ_CP047186.1|WP_082845206.1|1976348_1977332_-|tRNA-pseudouridine(55)-synthase-TruB
unknown
unknown
gnl|CDD|235113
NZ_CP047186.1|WP_132504125.1|1980046_1981468_+|RNB-domain-containing-ribonuclease
unknown
unknown
gnl|CDD|223631
NZ_CP047186.1|WP_132504119.1|1988196_1989963_-|proline--tRNA-ligase
unknown
unknown
gnl|CDD|236405
NZ_CP047186.1|WP_082844960.1|1986723_1987233_-|DUF2599-domain-containing-protein
unknown
unknown
gnl|CDD|378494
NZ_CP047186.1|WP_158286059.1|1987337_1987496_-|hypothetical-protein
unknown
unknown
unknown
NZ_CP047186.1|WP_068212040.1|1979125_1980007_+|A/G-specific-adenine-glycosylase
unknown
unknown
gnl|CDD|224115
NZ_CP047186.1|WP_132504121.1|1987532_1987778_-|hypothetical-protein
unknown
unknown
unknown
Protein
Cas_name
Cas_description
E-value
Identity
Coverage
Protein
Function_ID
Function_description
E-value
NZ_CP047186.1|WP_068208365.1|1990534_1991704_-|flavodoxin-dependent-(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase
gnl|CDD|234737
PRK00366, ispG, flavodoxin-dependent (E)-4-hydroxy-3-methylbut-2-enyl-diphosphate synthase.
0
NZ_CP047186.1|WP_132504128.1|1978489_1979089_-|hypothetical-protein
gnl|CDD|180660
PRK06696, PRK06696, uridine kinase; Validated.
1.05076e-30
NZ_CP047186.1|WP_082844959.1|1985108_1985411_-|YlxR-family-protein
gnl|CDD|377288
pfam04296, DUF448, Protein of unknown function (DUF448).
8.93542e-20
NZ_CP047186.1|WP_132504407.1|1991971_1993339_-|site-2-protease-family-protein
gnl|CDD|100084
cd06163, S2P-M50_PDZ_RseP-like, RseP-like Site-2 proteases (S2P), zinc metalloproteases (MEROPS family M50A), cleave transmembrane domains of substrate proteins, regulating intramembrane proteolysis (RIP) of diverse signal transduction mechanisms. In Escherichia coli, the S2P homolog RseP is involved in the sigmaE pathway of extracytoplasmic stress responses. Also included in this group are such homologs as Bacillus subtilis YluC, Mycobacterium tuberculosis Rv2869c S2P, and Bordetella bronchiseptica HurP. Rv2869c S2P appears to have a role in the regulation of prokaryotic lipid biosynthesis and membrane composition and YluC of Bacillus has a role in transducing membrane stress. This group includes bacterial and eukaryotic S2P/M50s homologs with either one or two PDZ domains present. PDZ domains are believed to have a regulatory role. The RseP PDZ domain is required for the inhibitory reaction that prevents cleavage of its substrate, RseA.
7.44097e-42
NZ_CP047186.1|WP_068208356.1|1985462_1986464_-|transcription-termination/antitermination-protein-NusA
gnl|CDD|237061
PRK12327, nusA, transcription elongation factor NusA; Provisional.
4.74889e-171
NZ_CP047186.1|WP_068212045.1|1977412_1978411_+|ketopantoate-reductase-family-protein
gnl|CDD|235821
PRK06522, PRK06522, 2-dehydropantoate 2-reductase; Reviewed.
7.33226e-47
NZ_CP047186.1|WP_068212053.1|1972838_1974386_-|SDR-family-oxidoreductase
gnl|CDD|187556
cd05245, SDR_a2, atypical (a) SDRs, subgroup 2. This subgroup contains atypical SDRs, one member is identified as Escherichia coli protein ybjT, function unknown. Atypical SDRs are distinct from classical SDRs. Members of this subgroup have a glycine-rich NAD(P)-binding motif consensus that generally matches the extended SDRs, TGXXGXXG, but lacks the characteristic active site residues of the SDRs. This subgroup has basic residues (HXXXR) in place of the active site motif YXXXK, these may have a catalytic role. Atypical SDRs generally lack the catalytic residues characteristic of the SDRs, and their glycine-rich NAD(P)-binding motif is often different from the forms normally seen in classical or extended SDRs. Atypical SDRs include biliverdin IX beta reductase (BVR-B,aka flavin reductase), NMRa (a negative transcriptional regulator of various fungi), progesterone 5-beta-reductase like proteins, phenylcoumaran benzylic ether and pinoresinol-lariciresinol reductases, phenylpropene synthases, eugenol synthase, triphenylmethane reductase, isoflavone reductases, and others. SDRs are a functionally diverse family of oxidoreductases that have a single domain with a structurally conserved Rossmann fold, an NAD(P)(H)-binding region, and a structurally diverse C-terminal region. Sequence identity between different SDR enzymes is typically in the 15-30% range; they catalyze a wide range of activities including the metabolism of steroids, cofactors, carbohydrates, lipids, aromatic compounds, and amino acids, and act in redox sensing. Classical SDRs have an TGXXX[AG]XG cofactor binding motif and a YXXXK active site motif, with the Tyr residue of the active site motif serving as a critical catalytic residue (Tyr-151, human 15-hydroxyprostaglandin dehydrogenase numbering). In addition to the Tyr and Lys, there is often an upstream Ser and/or an Asn, contributing to the active site; while substrate binding is in the C-terminal region, which determines specificity. The standard reaction mechanism is a 4-pro-S hydride transfer and proton relay involving the conserved Tyr and Lys, a water molecule stabilized by Asn, and nicotinamide. In addition to the Rossmann fold core region typical of all SDRs, extended SDRs have a less conserved C-terminal extension of approximately 100 amino acids, and typically have a TGXXGXXG cofactor binding motif. Complex (multidomain) SDRs such as ketoreductase domains of fatty acid synthase have a GGXGXXG NAD(P)-binding motif and an altered active site motif (YXXXN). Fungal type ketoacyl reductases have a TGXXXGX(1-2)G NAD(P)-binding motif.
2.1053e-123
NZ_CP047186.1|WP_068213513.1|1981464_1981896_-|30S-ribosome-binding-factor-RbfA
gnl|CDD|234787
PRK00521, rbfA, 30S ribosome-binding factor RbfA.
1.45277e-47
NZ_CP047186.1|WP_068212051.1|1974473_1975415_-|bifunctional-riboflavin-kinase/FAD-synthetase
gnl|CDD|235536
PRK05627, PRK05627, bifunctional riboflavin kinase/FAD synthetase.
4.18572e-122
NZ_CP047186.1|WP_132504119.1|1988196_1989963_-|proline--tRNA-ligase
gnl|CDD|236405
PRK09194, PRK09194, prolyl-tRNA synthetase; Provisional.
0
NZ_CP047186.1|WP_068208368.1|1993418_1994501_-|1-deoxy-D-xylulose-5-phosphate-reductoisomerase
gnl|CDD|235472
PRK05447, PRK05447, 1-deoxy-D-xylulose 5-phosphate reductoisomerase; Provisional.
0
NZ_CP047186.1|WP_082845206.1|1976348_1977332_-|tRNA-pseudouridine(55)-synthase-TruB
gnl|CDD|235113
PRK03287, truB, tRNA pseudouridine synthase B; Provisional.
2.35935e-133
NZ_CP047186.1|WP_132504125.1|1980046_1981468_+|RNB-domain-containing-ribonuclease
gnl|CDD|223631
COG0557, VacB, Exoribonuclease R [Transcription].
3.91179e-68
NZ_CP047186.1|WP_082844960.1|1986723_1987233_-|DUF2599-domain-containing-protein
gnl|CDD|378494
pfam10783, DUF2599, Protein of unknown function (DUF2599). This family is conserved in Actinobacteria. The function is not known.
4.97519e-23
NZ_CP047186.1|WP_068212040.1|1979125_1980007_+|A/G-specific-adenine-glycosylase
gnl|CDD|224115
COG1194, MutY, A/G-specific DNA glycosylase [DNA replication, recombination, and repair].
2.58107e-92
>NZ_CP047186.1|WP_068213513.1|1981464_1981896_-|30S-ribosome-binding-factor-RbfA
MADPARARKLAERIQVIVAKRLERGLRDPRLGFVTITDVQVTGDLQHASVFYTVYGTDEERADSAAALKAATGMLRTEVGKNITARLTPSLEFILDALPENAQHIEELLAAARSQDSQVQSLAAQADYAGEADPYVKPREDED
>NZ_CP047186.1|WP_132504125.1|1980046_1981468_+|RNB-domain-containing-ribonuclease
MTGRRLRLPRPDDDVDRALAAVRVAIDLPGAFPAEALAEAEHADANAEDGGRSDRTDLPFVTIDPPGSLDLDQALHLERTTDGVVLRYAIADVPAVVHSGGALDAEARRRGQTVYLPDGRIPLHPAVLSEGTASLLPDVRRRALVWTLTLDERAEPRSVRLERSLVRSVARLDYGAVQRSVEAGEPHPSIALLAWFGRERLAREAERGGASLTLPEEEIVAVGGGYRVERRAPLAVEAWNAQVSLLTGMVAARMMLGAGVGILRTMPAADPETVAAFRARAAALGTPWPTEEPYGAYLRRLDTGDPAQLAVMHAAATLFRGAGYTAFDGTPPEHPAQSALAAPYAHVTAPLRRLVDRFGLAVCLAVSNGDAVPDGLRAALPGLPPLLAASDRRAGAASRAATAIVEAAILRGREGASFTGVVVSSGRNRSAVQLLEPEITVDVQAPLLPGARVVVVLESVDVATGSAVFGLSA
>NZ_CP047186.1|WP_068212040.1|1979125_1980007_+|A/G-specific-adenine-glycosylase
MPSAALADVIVDWFRTSARDLPWRRDGFPAWGTLVSEFMLQQTPVVRVVPRLADWLERWPTPSALAAVPPGEAVRAWQSLGYPRRALRLHACAVAIAQEHGDVVPDDVDTLLALPGIGDYTARAIAVFAYGRRHPVVDTNVRRVIARAVDGAAEPGPPRAKADLAAMAALLPEPLPEAAAFNAGMMELGAVVCTARAPRCDECPIRHLCRWRADGYPEHTGPVKAPQKRFEGSDRQVRGLILAELRAAHAPVTAAEVESLWPDAQQRRRALAGLLADGLATGDPVDGYLLPGA
>NZ_CP047186.1|WP_132504128.1|1978489_1979089_-|hypothetical-protein
MTRWAPQKADVLDALAAEVLHNYGRGRVAVGVDGDDPAVSGVFALELAEALRRAGHDAIVAHLADFHRPRLERDDPSVPEEQRAYSGRYDYELLRRVLLDPFRLGGSTGFVLAGFDSVRDEARQACWRTAGQDAVLLVDGEFALRPELRGAWSTSIRLDTQEPPVDAAYRASTDPRRLATILVDIRDPEQPRRLFADSC
>NZ_CP047186.1|WP_068212045.1|1977412_1978411_+|ketopantoate-reductase-family-protein
MRIAVLGAGAVGGTVAALLDRAGHDVEVTARGEHLAAIRRSGLRLDGAWGEHTAWVRCGETLDLAPELAVVCTKAQDAEDALRANRRTVDGTLVVVVQNGLDGLQAAARQVRDARLVGALALFAASHLEPGRVSVTAAALTTLGVPGRPADDDVRRAAVVLGEAIPTETTDDFVGAQWTKLLINEVNALPAITGLSVQETVADPGLRRVLARALREAARTGIAAGVRFGTLQGLSHGSIRALAAAPLPVVELLPRRMAAGMGEVPNPGSTLQSIRRGVPSEIDHLAGAVVRTAERGGREARVNQLLVELVHEVERTGVFLPPADVVRRAALV
>NZ_CP047186.1|WP_082845206.1|1976348_1977332_-|tRNA-pseudouridine(55)-synthase-TruB
MLETPSPAPTAPAAVAATAPAASSAPNGILLLDKPGGITSHDLVSRTRRRAGTRKVGHAGTLDPMATGLMILGLGPSTRLLTYLVGLDKQYEATIRLGASTTTDDREGELLGSAEPALVAALAPEAVVDAVAALTGEIAQIPSTVSAIKVDGRRAYARVRDGEEVVLEARPVTVSSFDVLARREVDGFLDLDVRVTCSSGTYIRALARDLGAALGVGGHLTVLRRTAVGPFTVVRAGALDELDVPAALLPPAAAAGELFPLLRLESREAVDLANGKRIPAPEEVARVKGLLAAVGPGERLIGLAERRGTQLKSVVNFPTEELRTAAS
>NZ_CP047186.1|WP_068212047.1|1975983_1976352_-|hypothetical-protein
MIEWFTILQVGIAVAAGLLCLVLGLVGRRPSDVSVGATAIVELLLIVQLAVAIVSPLVGNRPSGSLPEYYVYLISALLLPLAAGFWALIERSRWSTLILGVACLSIAVMVYRMHQIWFVQSA
>NZ_CP047186.1|WP_068212049.1|1975414_1975933_-|hypothetical-protein
MSKPASEASGRAAHDPRLPSAPASADPSRSARSRGIGSLLVVVYGILALAATGRSLFQIIDRFDEAPLAFSLSALSAVVYIVATVALIVPGRAWQRVAWVTITFELVGVLVVGAVSVLEPQLLGLTSADPFGRQSTVWAAFGAGYLLIPLVLPVLGLWWLRVQGRRGPRAAS
>NZ_CP047186.1|WP_068212051.1|1974473_1975415_-|bifunctional-riboflavin-kinase/FAD-synthetase
MRVETRPGDLAGIGPSAVSIGKFDGVHAGHRAVIGTLHDRARERGLAAVVVTFDRNPLSVIAPEKCPPALVGNEQKLELLAGTGVDATLLLTFDEEFRALSPEEFVQHVLVDALEARVVLVGSDFRFGARGAGDIGMLRRLSEQHGFEVELIDDVRPEDGRRVSSTWIRELLAEGDVEHATRLLGHEPVVRGVVVHGAKRGRELGFPTANLSPQSQGLIPADGVYAGRLTTDGVTHPAAISVGSNPTFAGVPPKQVEAYVLDQTLETLDLYDRVVEVAFVGRIRGQVAYEGVEPLIRQMNDDVLRVREVLGIA
>NZ_CP047186.1|WP_068212053.1|1972838_1974386_-|SDR-family-oxidoreductase
MSQSPSDSTRPLALVTGATGYIGGRLTPRLLEAGFRVRVLVRDPRKLSDVPWAEEVEVAQGDLGDPESLTAAVDGVDVLYYLVHSMGSGNDHAHFEEVESRAAQNVASAAMAGGVGRIVYLGGLHPDGQELSKHLRSRAEVGRILMESGVPTIALQAGVIIGSGSTSFEMVRHLTDVLPYMPAPQWVRNFIQPIAVRDVLHYLIGAASLEDRRLNRTFDIGGPDVLRYGQMMNGYAVEAGLRQRPIASLPVFTPWLASQWVNLVTPIPRSLAVPIIASLQYDCVVHEQDIRSLIPDPEGGLTSYRRAVRLALGRMQAGEIETSWQNAEVVGAPSDPLPSDPEWAGHTVYVDLKVRRTQADPAKLWRVIEGIGGTNGWYSFPLAWVIRGWMDRLVGGVGLQRGRRDSARLHAGDALDFWRVEAIERPTLLRLRAEMKVPGGAWLEMRAEPSDGGGSVYTQRAVFFPQGLAGRLYWFAILPFHGVIFNGMANRITATAADLPDSGDERSPGGRRAQR
>NZ_CP047186.1|WP_082844959.1|1985108_1985411_-|YlxR-family-protein
MSPVRTCVGCRLRAPRASLLRLVLHSNVLAVDPRAVRPGRGAWLHDSADCYGLAVKRRAFGRAFRTRESVDASELEQYVMRVRTGSVPHPEGPEQRTITP
>NZ_CP047186.1|WP_068208356.1|1985462_1986464_-|transcription-termination/antitermination-protein-NusA
MDIDLSVLRLMEREREIPFEELVQIIEQAILTAYLKHIGQADDADKSTAVSARVHLDRKTGHVSVFVPEYDDEGAVVGEAEDSPRDFGRIAAFAAKQVINQRLRDIADEHVLGEFKGREGDIVAGVIQQGPNPRMIHVDLGSIEAILSPEEQVPGEDYSHGRRIRVYVTSVGRGAKGPSVQVSRTHPSLVRKLFALEVPEIASGVVEIVSLAREAGHRTKIAVRATEPGVNAKGACIGELGQRVRAVTAELNNEKIDIVDYSSDLPTFVASALSPAKVTSAFVIDQGLKAVRALVPDYQLSLAIGKEGQNARLAAKLTGAKIDIQPDSVMDGE
>NZ_CP047186.1|WP_082844960.1|1986723_1987233_-|DUF2599-domain-containing-protein
MAAAQAACSTSPASGADEGRWARDANGTSIPTHYDVTGTTLTQIVDLSQPDIAFPVVADPWFGRNLIDHVTWVPGDPQWGPTAQVYPTDYGRDQIAVGPEANEAAWGEALEKGDRSRLDHNNLHDHFSCHFLGRSSTVGKESWNLDNNRPDVGLAATIAASCNPQGGED
>NZ_CP047186.1|WP_158286059.1|1987337_1987496_-|hypothetical-protein
MPDSLSIALTAAFALSVAGFVTVVASAVVSLRRARRQDPTTRVRSTTALAGA
>NZ_CP047186.1|WP_132504121.1|1987532_1987778_-|hypothetical-protein
MNASHDQVKKTLQIGAAVSAVSLLAGAVFVPLLILAVVAVIASAIVAAAISCRATHRWAWTWVAGVASVVWVSSAIYAFDV
>NZ_CP047186.1|WP_132504119.1|1988196_1989963_-|proline--tRNA-ligase
MVTRLSHLFVRTLREDPADAEVAGHRLLVRAGYIRRQAPGVFAWLPLGLRVKRRIERILHEEMEAAGAQEVHFPALLPREPYELTGRWTEYGDGVFRLKDRKDADYMLAPTHEEFFTLLVKDLYSSYKDLPLSIYQIQDKYRDEARPRAGLLRGREFTMKDAYSFDYTDAGLDASYQRQRDAYERIFARLGLEYVIVQADAGAMGGSRSEEFLHPTPVGEDTFVRSAGGYAANVEAYRTPVPEASPVEGRPEARVFDSPDTPTIQTLVDLANATQPRTDGRAWTAGDTLKNVVLALTALDGTRELVIVGLPGDRDVDLKRAEVAFAPAEVEAATAEDFAKHPGLVKGYIGPWSSEGAVLGEESATGVRYLLDPRVVDGTAWITGANVSGQHVLDLLAGRDFHADGTVEVAEVRTGDEAPDGSGPIETARGMEIGHVFQLGRKYAEVLGLKVLDENGKLVTVTMGSYGIGVTRILAIIAESTHDERGLLWPANVAPFDVHVIATGKDAAALELAESVGASLEAAGRDVLIDDRPKVSPGVKFGDAELIGVPVIVIAGRGAADGIVELWDRRSGEREQLPVAEALARLGA
>NZ_CP047186.1|WP_068208362.1|1990030_1990513_-|hypothetical-protein
MVRPALLLAFGVVAVTLVASGVAALRSTPAPLSDDCVDLRTAQDPFGCDGWVLTAAEGETPYSAWVEDARVRLRSERVAGEPTLVVGTDCLVLRASYRIEGTVLVPSDEVTGSDTCSDTPSPAGIRLRALLSAPITLGGTPDDVVLDGTRGAVVFSRIPG
>NZ_CP047186.1|WP_068208365.1|1990534_1991704_-|flavodoxin-dependent-(E)-4-hydroxy-3-methylbut-2-enyl-diphosphate-synthase
MGRVPAVNLGLPKVPMTLAPRRKSRQIKVGKVLVGGDAQVSVQSMCTTPTTNINATLQQIAELTASGCDIVRVAVPSRDDAEALPIIAKKSQIPVIADIHFQPNYVYAAIDAGCAAVRVNPGNIRKFDDQVGKIAAAAKAAGVSIRIGVNAGSLEPSILQKYGKPTPEALVESAVWEASLFEEHDFHDFKISVKHNDPVVMVKAYRQLAERGDWPLHLGVTEAGPEFQGTIKSATAFGILLGEGIGDTIRVSLSAPPAQEVKVGLQILQSLNLRERKLEIVSCPSCGRAQVDVYTLANDVTAGLEGMSVPLRVAVMGCVVNGPGEAREADLGVASGNGKGQIFVKGEVIKTVPEAEIVQTLIEEANRLAAEMPADDTSTGAPVVTVGAN
>NZ_CP047186.1|WP_132504407.1|1991971_1993339_-|site-2-protease-family-protein
MLLFVLGVVIIAIGVALSIALHEVGHLVPAKLFGVKVTQYMIGFGPTIFSRRRGETEYGVKALPLGGYIAMIGMYPPKHAGDPITESPVGLFQGVGYQSSEKRTAGRPTLIDEARAASAETIGEGEEHRAFYLLPVWKRVIVMAGGPFMNLLIATVLFTVLLCGIGVAQSTSTLASVSQCVVPESQRATATCTADDPLAPGAAAGLLPGDTITAIDGTPVGTWNDLTPIIQRSAGVPLSVAVERDGASLTLSITPAENEVAVTDSAGNPVTDASGAVETQTVGFIGISPTSELARQPITAVPGTVWQNITSVAHVILNLPQRLIDVAQAAFGTEARDANGPISVVGVGRIAGEIAASDQLPIVSKVQTMVGVLASLNVALLVFNLVPLLPMDGGHIAGALWEGLRRRIAKLFGRRDPGPVDIARLLPLTYIVVLVLGGMSALLIYADIVKPITLF
>NZ_CP047186.1|WP_068208368.1|1993418_1994501_-|1-deoxy-D-xylulose-5-phosphate-reductoisomerase
MRRVIILGSTGSIGTQALDVIGANLDRFEVVGLAAGSNRPVVAEQAAAFGVEHTAFGADEAEQLIRSVEADVVLNGITGSVGLGPTLAALEEGRTLALANKESLIVGGELVTSLAAPGQIVPVDSEHSAIAQALLAGAHREVRRLVLTASGGPFRGRDRGSLRDVTPAEALAHPTWDMGLVVTTNSSTLVNKGLEVIEAHLLFDVPYHRIDVTVHPQSVIHSMVEYVDGSTIAQASPPDMRLPISLGLDWPHRVAGVGAPLDWTRSHSWTFEPLDEEAFPAVRLAKRVGEAGASYPAVFNAANEQAVQAFHAGRIGYLDILATVEAVVDAHAVDGALTRQSLAAAEEWARRAADARIAGT