CYP5348J3

Insight into CYP534

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping

Substrate

Δ6-protoilludene

PubChem ↗ Cc1cc(O)cc(O)c1C(=O)OCC1=CC2CC(C)(C)C(O)C2C2(C)CC(O)C12O

CYP5348J3

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

Δ6-protoilludene-5-ol

PubChem ↗ Crowdsource product structure

Evidence trail

Excerpts are machine-extracted plain text for biochemical provenance. Follow DOI / PubMed links for the primary literature; publisher figures and PDF images are not displayed here.

Source text excerpt ation; ation; Coexpression in S. cerevisiae; product identified by NMR and GC-MS.

Reaction & quality gates

Mechanism: Hydroxylation
Evidence type: In vitro
Confidence: High
Data tier: Silver
mass=no_smiles; incomplete_SMILES
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:30105900 ↗
DOI: 10.1111/1751-7915.13304 ↗
UniProt: —
GenBank: —
NCBI TaxID: —

Insight into metabolic diversity of the brown-rot basidiomycete Postia placenta responsible for sesquiterpene biosynthesis: semi-comprehensive screening of cytochrome P450 monooxygenase involved in protoilludene metabolism.