CYP716C87

Nicotiana attenuata CYP716C

Solanaceae

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

Substrate

oleanolic acid

PubChem ↗ C[C@]12CC[C@@H](C([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C…

CYP716C87

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

maslinic acid

PubChem ↗ C[C@@]12CC[C@@H]3[C@@]([C@H]1CC=C4[C@]2(CC[C@@]5([C@H]4CC(CC5)(…

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; Heterologous expression in Nicotiana benthamiana; confirmed with authentic standard.

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: Organic acids
Product class: Organic acids

Literature & public identifiers

PubMed: PMID:39052981 ↗
DOI: 10.1093/plphys/kiae399 ↗
UniProt: —
GenBank: —
NCBI TaxID: 49451 ↗

Roles of three cytochrome P450 monooxygenases in triterpene biosynthesis and their potential impact on growth and development.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme