CYP12

Biosynthesis and CYP12

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

Substrate

δ-guaiene

PubChem ↗ CC1CCC2=C(CCC(CC12)C(=C)C)C

CYP12

ΔMass: +18.0106 Da mismatch

Product

globulol

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

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, α-humulene, and alloaromadendrene; efficiency 66±19% in C. reinhardtii plastid

Reaction & quality gates

Mechanism: Hydroxylation
Evidence type: In vivo
Confidence: High
Data tier: Silver
mass=mismatch
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