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STCG_EMENI
ID   STCG_EMENI              Reviewed;         305 AA.
AC   A0A1U8QGV2; C8VDU1; Q5AV63;
DT   25-MAY-2022, integrated into UniProtKB/Swiss-Prot.
DT   10-MAY-2017, sequence version 1.
DT   03-AUG-2022, entry version 15.
DE   RecName: Full=5'-hydroxyaverantin dehydrogenase stcG {ECO:0000250|UniProtKB:P87017};
DE            Short=HAVN dehydrogenase {ECO:0000250|UniProtKB:P87017};
DE            EC=1.1.1.352 {ECO:0000250|UniProtKB:P87017};
DE   AltName: Full=Sterigmatocystin biosynthesis cluster protein G {ECO:0000303|PubMed:8643646};
GN   Name=swtcG {ECO:0000303|PubMed:8900026}; ORFNames=AN7817;
OS   Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 /
OS   M139) (Aspergillus nidulans).
OC   Eukaryota; Fungi; Dikarya; Ascomycota; Pezizomycotina; Eurotiomycetes;
OC   Eurotiomycetidae; Eurotiales; Aspergillaceae; Aspergillus;
OC   Aspergillus subgen. Nidulantes.
OX   NCBI_TaxID=227321;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RC   STRAIN=FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139;
RX   PubMed=16372000; DOI=10.1038/nature04341;
RA   Galagan J.E., Calvo S.E., Cuomo C., Ma L.-J., Wortman J.R., Batzoglou S.,
RA   Lee S.-I., Bastuerkmen M., Spevak C.C., Clutterbuck J., Kapitonov V.,
RA   Jurka J., Scazzocchio C., Farman M.L., Butler J., Purcell S., Harris S.,
RA   Braus G.H., Draht O., Busch S., D'Enfert C., Bouchier C., Goldman G.H.,
RA   Bell-Pedersen D., Griffiths-Jones S., Doonan J.H., Yu J., Vienken K.,
RA   Pain A., Freitag M., Selker E.U., Archer D.B., Penalva M.A., Oakley B.R.,
RA   Momany M., Tanaka T., Kumagai T., Asai K., Machida M., Nierman W.C.,
RA   Denning D.W., Caddick M.X., Hynes M., Paoletti M., Fischer R., Miller B.L.,
RA   Dyer P.S., Sachs M.S., Osmani S.A., Birren B.W.;
RT   "Sequencing of Aspergillus nidulans and comparative analysis with A.
RT   fumigatus and A. oryzae.";
RL   Nature 438:1105-1115(2005).
RN   [2]
RP   GENOME REANNOTATION.
RC   STRAIN=FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139;
RX   PubMed=19146970; DOI=10.1016/j.fgb.2008.12.003;
RA   Wortman J.R., Gilsenan J.M., Joardar V., Deegan J., Clutterbuck J.,
RA   Andersen M.R., Archer D., Bencina M., Braus G., Coutinho P., von Dohren H.,
RA   Doonan J., Driessen A.J., Durek P., Espeso E., Fekete E., Flipphi M.,
RA   Estrada C.G., Geysens S., Goldman G., de Groot P.W., Hansen K.,
RA   Harris S.D., Heinekamp T., Helmstaedt K., Henrissat B., Hofmann G.,
RA   Homan T., Horio T., Horiuchi H., James S., Jones M., Karaffa L.,
RA   Karanyi Z., Kato M., Keller N., Kelly D.E., Kiel J.A., Kim J.M.,
RA   van der Klei I.J., Klis F.M., Kovalchuk A., Krasevec N., Kubicek C.P.,
RA   Liu B., Maccabe A., Meyer V., Mirabito P., Miskei M., Mos M., Mullins J.,
RA   Nelson D.R., Nielsen J., Oakley B.R., Osmani S.A., Pakula T., Paszewski A.,
RA   Paulsen I., Pilsyk S., Pocsi I., Punt P.J., Ram A.F., Ren Q., Robellet X.,
RA   Robson G., Seiboth B., van Solingen P., Specht T., Sun J.,
RA   Taheri-Talesh N., Takeshita N., Ussery D., vanKuyk P.A., Visser H.,
RA   van de Vondervoort P.J., de Vries R.P., Walton J., Xiang X., Xiong Y.,
RA   Zeng A.P., Brandt B.W., Cornell M.J., van den Hondel C.A., Visser J.,
RA   Oliver S.G., Turner G.;
RT   "The 2008 update of the Aspergillus nidulans genome annotation: a community
RT   effort.";
RL   Fungal Genet. Biol. 46:S2-13(2009).
RN   [3]
RP   FUNCTION, AND INDUCTION.
RX   PubMed=8017929; DOI=10.1128/aem.60.5.1444-1450.1994;
RA   Keller N.P., Kantz N.J., Adams T.H.;
RT   "Aspergillus nidulans verA is required for production of the mycotoxin
RT   sterigmatocystin.";
RL   Appl. Environ. Microbiol. 60:1444-1450(1994).
RN   [4]
RP   FUNCTION.
RX   PubMed=7486998; DOI=10.1128/aem.61.10.3628-3632.1995;
RA   Keller N.P., Segner S., Bhatnagar D., Adams T.H.;
RT   "StcS, a putative P-450 monooxygenase, is required for the conversion of
RT   versicolorin A to sterigmatocystin in Aspergillus nidulans.";
RL   Appl. Environ. Microbiol. 61:3628-3632(1995).
RN   [5]
RP   FUNCTION.
RC   STRAIN=FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139;
RX   PubMed=7642507; DOI=10.1128/jb.177.16.4792-4800.1995;
RA   Yu J.-H., Leonard T.J.;
RT   "Sterigmatocystin biosynthesis in Aspergillus nidulans requires a novel
RT   type I polyketide synthase.";
RL   J. Bacteriol. 177:4792-4800(1995).
RN   [6]
RP   FUNCTION.
RX   PubMed=8900026; DOI=10.1128/aem.62.11.4296-4298.1996;
RA   Kelkar H.S., Keller N.P., Adams T.H.;
RT   "Aspergillus nidulans stcP encodes an O-methyltransferase that is required
RT   for sterigmatocystin biosynthesis.";
RL   Appl. Environ. Microbiol. 62:4296-4298(1996).
RN   [7]
RP   FUNCTION.
RX   PubMed=8962148; DOI=10.1073/pnas.93.25.14873;
RA   Brown D.W., Adams T.H., Keller N.P.;
RT   "Aspergillus has distinct fatty acid synthases for primary and secondary
RT   metabolism.";
RL   Proc. Natl. Acad. Sci. U.S.A. 93:14873-14877(1996).
RN   [8]
RP   INDUCTION, FUNCTION, AND PATHWAY.
RX   PubMed=8643646; DOI=10.1073/pnas.93.4.1418;
RA   Brown D.W., Yu J.-H., Kelkar H.S., Fernandes M., Nesbitt T.C., Keller N.P.,
RA   Adams T.H., Leonard T.J.;
RT   "Twenty-five coregulated transcripts define a sterigmatocystin gene cluster
RT   in Aspergillus nidulans.";
RL   Proc. Natl. Acad. Sci. U.S.A. 93:1418-1422(1996).
RN   [9]
RP   FUNCTION.
RX   PubMed=8999832; DOI=10.1074/jbc.272.3.1589;
RA   Kelkar H.S., Skloss T.W., Haw J.F., Keller N.P., Adams T.H.;
RT   "Aspergillus nidulans stcL encodes a putative cytochrome P-450
RT   monooxygenase required for bisfuran desaturation during
RT   aflatoxin/sterigmatocystin biosynthesis.";
RL   J. Biol. Chem. 272:1589-1594(1997).
RN   [10]
RP   FUNCTION.
RX   PubMed=10618248; DOI=10.1128/aem.66.1.359-362.2000;
RA   Keller N.P., Watanabe C.M., Kelkar H.S., Adams T.H., Townsend C.A.;
RT   "Requirement of monooxygenase-mediated steps for sterigmatocystin
RT   biosynthesis by Aspergillus nidulans.";
RL   Appl. Environ. Microbiol. 66:359-362(2000).
RN   [11]
RP   REVIEW ON STERIGMATOCYSTIN BIOSYNTHESIS.
RX   PubMed=24957370; DOI=10.3390/metabo2010100;
RA   Klejnstrup M.L., Frandsen R.J., Holm D.K., Nielsen M.T., Mortensen U.H.,
RA   Larsen T.O., Nielsen J.B.;
RT   "Genetics of polyketide metabolism in Aspergillus nidulans.";
RL   Metabolites 2:100-133(2012).
CC   -!- FUNCTION: 5'-hydroxyaverantin dehydrogenase; part of the gene cluster
CC       that mediates the biosynthesis of sterigmatocystin (ST), a polyketide-
CC       derived furanocoumarin which is part of the most toxic and carcinogenic
CC       compounds among the known mycotoxins (PubMed:8643646). The first step
CC       in the biosynthesis of sterigmatocystin is the production of hexanoate
CC       by the fatty acid synthase (FAS) units stcJ and stcK (PubMed:8962148).
CC       The polyketide backbone is assembled by the non-reducing polyketide
CC       synthase stcA by condensation of the starter hexanoyl-CoA and 7
CC       malonyl-CoA extender units followed by cyclization and release of
CC       norsolorinic acid (By similarity). Norsolorinic acid is the first
CC       stable intermediate in the biosynthesis of sterigmatocystin and is
CC       converted into averantin (AVN) by the ketoreductase stcE which reduces
CC       the hexanoate ketone to an alcohol (PubMed:8643646) (Probable).
CC       Averantin is then oxidized into 5'-hydroxyaverantin (HAVN) by the
CC       cytochrome P450 monooxygenase stcF (PubMed:10618248). 5'-
CC       hydroxyaverantin is further converted to 5'-oxyaverantin (OAVN) by the
CC       5'-hydroxyaverantin dehydrogenase stcG (PubMed:24957370). The next step
CC       is the conversion of OAVN into averufin (AVF) which is catalyzed by a
CC       yet to be identified enzyme (PubMed:24957370). The cytochrome P450
CC       monoxygenase stcB and the flavin-binding monooxygenase stcW are both
CC       required for the conversion of averufin to 1-hydroxyversicolorone
CC       (PubMed:10618248). The esterase stcI probably catalyzes the formation
CC       of versiconal hemiacetal acetate from 1-hydroxyversicolorone
CC       (PubMed:24957370). The oxydoreductase stcN then probably catalyzes the
CC       biosynthetic step from versiconal to versicolorin B (VERB)
CC       (PubMed:24957370). The next step is performed by the versicolorin B
CC       desaturase stcL to produce versicolorin A (VERA) (PubMed:8999832). The
CC       ketoreductase stcU and the cytochrome P450 monooxygenase stcS are
CC       involved in the conversion of versicolorin A to
CC       demethylsterigmatocystin (PubMed:7486998). The Baeyer-Villiger oxidas
CC       stcQ and the reductase stcR might be involved in the biosynthetic step
CC       from versicolorin A to demethylsterigmatocystin (PubMed:24957370). The
CC       final step in the biosynthesis of sterigmatocystin is the methylation
CC       of demethylsterigmatocystin catalyzed by the methyltransferase stcP
CC       (PubMed:8900026). {ECO:0000250|UniProtKB:Q12053,
CC       ECO:0000269|PubMed:10618248, ECO:0000269|PubMed:7486998,
CC       ECO:0000269|PubMed:8643646, ECO:0000269|PubMed:8900026,
CC       ECO:0000269|PubMed:8962148, ECO:0000269|PubMed:8999832,
CC       ECO:0000303|PubMed:24957370, ECO:0000305|PubMed:8643646}.
CC   -!- CATALYTIC ACTIVITY:
CC       Reaction=(1'S,5'S)-5'-hydroxyaverantin + NAD(+) = (S)-5'-oxoaverantin +
CC         H(+) + NADH; Xref=Rhea:RHEA:35475, ChEBI:CHEBI:15378,
CC         ChEBI:CHEBI:57540, ChEBI:CHEBI:57945, ChEBI:CHEBI:77900,
CC         ChEBI:CHEBI:77933; EC=1.1.1.352;
CC         Evidence={ECO:0000250|UniProtKB:P87017};
CC   -!- CATALYTIC ACTIVITY:
CC       Reaction=(1'S,5'R)-5'-hydroxyaverantin + NAD(+) = (S)-5'-oxoaverantin +
CC         2 H(+) + NADH; Xref=Rhea:RHEA:35479, ChEBI:CHEBI:15378,
CC         ChEBI:CHEBI:57540, ChEBI:CHEBI:57945, ChEBI:CHEBI:71536,
CC         ChEBI:CHEBI:77933; EC=1.1.1.352;
CC         Evidence={ECO:0000250|UniProtKB:P87017};
CC   -!- PATHWAY: Mycotoxin biosynthesis; sterigmatocystin biosynthesis.
CC       {ECO:0000269|PubMed:8643646}.
CC   -!- INDUCTION: The genes forming the sterigmatocystin biosynthesis cluster
CC       are co-regulated and induced on oatmeal porridge or the fungal isolates
CC       were grown either on oatmeal porridge or in YEC medium (0.2% yeast
CC       extract, 5.0% corn steep liquor). {ECO:0000269|PubMed:8017929,
CC       ECO:0000269|PubMed:8643646}.
CC   -!- SIMILARITY: Belongs to the short-chain dehydrogenases/reductases (SDR)
CC       family. {ECO:0000305}.
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DR   EMBL; BN001304; CBF80169.1; -; Genomic_DNA.
DR   EMBL; AACD01000132; EAA61605.1; -; Genomic_DNA.
DR   RefSeq; XP_681086.1; XM_675994.1.
DR   STRING; 162425.CADANIAP00000960; -.
DR   EnsemblFungi; CBF80169; CBF80169; ANIA_07817.
DR   GeneID; 2869365; -.
DR   KEGG; ani:AN7817.2; -.
DR   VEuPathDB; FungiDB:AN7817; -.
DR   eggNOG; KOG0725; Eukaryota.
DR   HOGENOM; CLU_010194_13_3_1; -.
DR   InParanoid; A0A1U8QGV2; -.
DR   OMA; YNTCYLA; -.
DR   OrthoDB; 1210617at2759; -.
DR   UniPathway; UPA00377; -.
DR   Proteomes; UP000000560; Chromosome IV.
DR   Proteomes; UP000005890; Unassembled WGS sequence.
DR   GO; GO:0016491; F:oxidoreductase activity; IEA:UniProtKB-KW.
DR   GO; GO:0045461; P:sterigmatocystin biosynthetic process; IEP:GO_Central.
DR   InterPro; IPR036291; NAD(P)-bd_dom_sf.
DR   InterPro; IPR020904; Sc_DH/Rdtase_CS.
DR   InterPro; IPR002347; SDR_fam.
DR   Pfam; PF00106; adh_short; 1.
DR   PRINTS; PR00081; GDHRDH.
DR   SUPFAM; SSF51735; SSF51735; 1.
DR   PROSITE; PS00061; ADH_SHORT; 1.
PE   2: Evidence at transcript level;
KW   NAD; NADP; Oxidoreductase; Reference proteome.
FT   CHAIN           1..305
FT                   /note="5'-hydroxyaverantin dehydrogenase stcG"
FT                   /id="PRO_0000455265"
FT   ACT_SITE        186
FT                   /note="Proton acceptor"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU10001"
FT   BINDING         20..48
FT                   /ligand="NADP(+)"
FT                   /ligand_id="ChEBI:CHEBI:58349"
FT                   /evidence="ECO:0000250|UniProtKB:P16544"
FT   BINDING         190
FT                   /ligand="NADP(+)"
FT                   /ligand_id="ChEBI:CHEBI:58349"
FT                   /evidence="ECO:0000250|UniProtKB:P16544"
SQ   SEQUENCE   305 AA;  32640 MW;  2DC794D0F5432708 CRC64;
     MEPLDLTCDL TSLNGKSAFI TGGASGLGLA TARKWAEAGV YITIADIQPP TSPVQPGLAH
     CFHYVYCDVT SWESQVAAFK SALRFSPSGA LDIVACFAGT ALAPGNQIDH VLAAGVPSLE
     VDPPRPSSSV RNIEVNLVGS YFTSWLGLYY LRIPGTGTDP ELPSNKCLLF CASIAAYMDS
     PKASTYPASK FGVRGLFRST RSQTKQLGVR CNLLAPWFFD SPLIAPIKHA MAARGVDMAK
     VLTFTSIDAC VDAATYCVAS PEIHGRALAV QPEGTFDLKD DLEDGWGGNQ LRPIMQRRRD
     AGFDV
 
 
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