CYP716C87

Nicotiana attenuata CYP716C

Solanaceae

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

Substrate

betulinic acid

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

CYP716C87

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

alphitolic acid

PubChem ↗ CC(=C)[C@@H]1CC[C@]2([C@H]1[C@H]3CC[C@H]4[C@]([C@@]3(CC2)C)(CC[…

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; putative identification based on EI-MS and characteristic fragment m/z 320.

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: Terpenoids
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