CYP12

Biosynthesis and CYP12

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

Substrate

alloaromadendrene

PubChem ↗ C[C@@H]1CC[C@H]2[C@@H]1[C@H]3[C@H](C3(C)C)CCC2=C

CYP12

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

alloaromadendrene oxide

PubChem ↗ C[C@@H]1CC[C@H]2[C@H]1[C@H]3[C@H](C3(C)C)CCC24CO4

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; UniProt: E3W9C4; also acts on α-guaiene, β-guaiene, δ-guaiene, and α-humulene; efficiency 66±19% in C. reinhardtii plastid

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vivo
Confidence: High
Data tier: Gold
Latin binomial + experiment + dual SMILES + ΔMass pass
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:39589357 ↗
DOI: 10.1002/cbic.202400902 ↗
UniProt: A0A0N7F296 ↗
GenBank: —
NCBI TaxID: —

Compartmentalized Sesquiterpenoid Biosynthesis and Functionalization in the Chlamydomonas reinhardtii Plastid.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme