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OLCK_PENCN
ID   OLCK_PENCN              Reviewed;         302 AA.
AC   P9WEP3;
DT   29-SEP-2021, integrated into UniProtKB/Swiss-Prot.
DT   29-SEP-2021, sequence version 1.
DT   03-AUG-2022, entry version 3.
DE   RecName: Full=Dioxygenase olcK {ECO:0000303|PubMed:30090271};
DE            EC=1.14.11.- {ECO:0000269|PubMed:30090271};
DE   AltName: Full=15-deoxyoxalicine B biosynthesis cluster protein K {ECO:0000303|PubMed:30090271};
GN   Name=olcK {ECO:0000303|PubMed:30090271};
OS   Penicillium canescens.
OC   Eukaryota; Fungi; Dikarya; Ascomycota; Pezizomycotina; Eurotiomycetes;
OC   Eurotiomycetidae; Eurotiales; Aspergillaceae; Penicillium.
OX   NCBI_TaxID=5083;
RN   [1]
RP   FUNCTION, DISRUPTION PHENOTYPE, SUBCELLULAR LOCATION, AND PATHWAY.
RX   PubMed=30090271; DOI=10.1039/c5sc01965f;
RA   Yaegashi J., Romsdahl J., Chiang Y.M., Wang C.C.C.;
RT   "Genome mining and molecular characterization of the biosynthetic gene
RT   cluster of a diterpenic meroterpenoid, 15-deoxyoxalicine B, in Penicillium
RT   canescens.";
RL   Chem. Sci. 6:6537-6544(2015).
RN   [2]
RP   ERRATUM OF PUBMED:30090271.
RX   PubMed=30123464; DOI=10.1039/c6sc90012g;
RA   Yaegashi J., Romsdahl J., Chiang Y.M., Wang C.C.C.;
RT   "Correction: Genome mining and molecular characterization of the
RT   biosynthetic gene cluster of a diterpenic meroterpenoid, 15-deoxyoxalicine
RT   B, in Penicillium canescens.";
RL   Chem. Sci. 7:2440-2440(2016).
CC   -!- FUNCTION: Dioxygenase; part of the gene cluster that mediates the
CC       biosynthesis of 15-deoxyoxalicine B (PubMed:30090271). The first step
CC       of the pathway is the synthesis of nicotinyl-CoA from nicotinic acid by
CC       the nicotinic acid-CoA ligase olcI (PubMed:30090271). Nicotinyl-CoA is
CC       then a substrate of polyketide synthase olcA to produce 4-hydroxy-6-(3-
CC       pyridinyl)-2H-pyran-2-one (HPPO) which is further prenylated by the
CC       polyprenyl transferase olcH to yield geranylgeranyl-HPPO
CC       (PubMed:30090271). Geranylgeranyl pyrophosphate is provided by the
CC       cluster-specific geranylgeranyl pyrophosphate synthase olcC
CC       (PubMed:30090271). The FAD-dependent monooxygenase olcE catalyzes the
CC       epoxidation of geranylgeranyl-HPPO and the terpene cyclase olcD
CC       catalyzes the cyclization of the terpenoid component, resulting in the
CC       formation of the tricyclic terpene moiety seen in predecaturin E
CC       (PubMed:30090271). The cytochrome P450 monooxygenase then catalyzes the
CC       allylic oxidation of predecaturin E, which is followed by
CC       spirocylization with concomitant loss of one molecule of water to form
CC       decaturin E (PubMed:30090271). Decaturin E is the substrate of the
CC       cytochrome P450 monooxygenase olcJ which hydroxylates it at the C-29
CC       position to form decaturin F (PubMed:30090271). The short-chain
CC       dehydrogenase/reductase olcF may catalyze the oxidation of decaturin F
CC       to generate the 29-hydroxyl-27-one intermediate, and subsequent
CC       hemiacetal formation probably leads to the formation of decaturin C
CC       (Probable). The dioxygenase olcK may be a peroxisomal enzyme that
CC       catalyzes the hydroxylation of decaturin C into decaturin A once
CC       decaturin C is shuttled into the peroxisome by the MFS transporter olcL
CC       (Probable). Finally the cytochrome P450 monooxygenase olcB catalyzes
CC       the oxidative rearrangement to yield 15-deoxyoxalicine B
CC       (PubMed:30090271). In the absence of olcJ, decaturin E may be shunted
CC       to a pathway in which it is oxidized to a ketone, possibly by olcF, to
CC       form decaturin D, which undergoes further allylic oxidation to yield
CC       decaturin G (PubMed:30090271). Moreover, in the absence of oclK or
CC       oclL, oclB can convert decaturin C into 15-deoxyoxalicine A
CC       (PubMed:30090271). {ECO:0000269|PubMed:30090271,
CC       ECO:0000305|PubMed:30090271}.
CC   -!- COFACTOR:
CC       Name=Fe cation; Xref=ChEBI:CHEBI:24875;
CC         Evidence={ECO:0000250|UniProtKB:A0A097ZPD9};
CC   -!- PATHWAY: Secondary metabolite biosynthesis; terpenoid biosynthesis.
CC       {ECO:0000269|PubMed:30090271}.
CC   -!- SUBUNIT: Homodimer. {ECO:0000250|UniProtKB:Q4WAW9}.
CC   -!- SUBCELLULAR LOCATION: Peroxisome matrix {ECO:0000305|PubMed:30090271}.
CC   -!- DISRUPTION PHENOTYPE: Abolishes the production of 15-deoxyoxalicine B
CC       and accumulates decaturin C and 5-deoxyoxalicine A.
CC       {ECO:0000269|PubMed:30090271}.
CC   -!- MISCELLANEOUS: The 15-deoxyoxalicine B cluster is a rare cluster that
CC       contains its own geranylgeranyl pyrophosphate synthase (olcC), in
CC       contrast to other related clusters which rely on a FPP/GGPP synthase
CC       localized outside of the cluster. {ECO:0000269|PubMed:30090271}.
CC   -!- SIMILARITY: Belongs to the PhyH family. {ECO:0000305}.
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DR   SMR; P9WEP3; -.
DR   UniPathway; UPA00213; -.
DR   GO; GO:0005782; C:peroxisomal matrix; IEA:UniProtKB-SubCell.
DR   GO; GO:0051213; F:dioxygenase activity; IEA:UniProtKB-KW.
DR   GO; GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.
DR   GO; GO:0016114; P:terpenoid biosynthetic process; IEA:UniProtKB-UniPathway.
DR   InterPro; IPR008775; Phytyl_CoA_dOase.
DR   Pfam; PF05721; PhyH; 1.
PE   3: Inferred from homology;
KW   Dioxygenase; Iron; Metal-binding; Oxidoreductase; Peroxisome.
FT   CHAIN           1..302
FT                   /note="Dioxygenase olcK"
FT                   /id="PRO_0000453895"
FT   BINDING         136
FT                   /ligand="Fe cation"
FT                   /ligand_id="ChEBI:CHEBI:24875"
FT                   /evidence="ECO:0000250|UniProtKB:O14832"
FT   BINDING         138
FT                   /ligand="Fe cation"
FT                   /ligand_id="ChEBI:CHEBI:24875"
FT                   /evidence="ECO:0000250|UniProtKB:O14832"
FT   BINDING         213
FT                   /ligand="Fe cation"
FT                   /ligand_id="ChEBI:CHEBI:24875"
FT                   /evidence="ECO:0000250|UniProtKB:O14832"
SQ   SEQUENCE   302 AA;  33969 MW;  EA8FE0AC29741D13 CRC64;
     MTIVSPDKLP SARAVELTAP LDDIYQILNE DGAVIIKNFI PLELVDKINK EVDPYLAQHA
     AGPNHMSEIY KLTVGSKTKH MGNLTMASKS FRDEVLNHPS MHAISEKLFR ANFGDYWLNR
     AAVLEVDSGE KAQGLHRDDS LYPWKAFLTK DSPELMVNFF IALTEFREEN GATRLVLGSH
     KWEDSTRYPS PEQTIPAEMQ AGDAIVYLAS LFHGAGQNRS QKTRRGLSIT THPAHFTPME
     SHIDVPRAII ENMTPLAQKM IGWRTWSTNH GVPVWTVRDG RMEDELKLKS LESPKQIQAA
     VI
 
 
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