CYP716A419

Nicotiana attenuata CYP716A

Solanaceae

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

Substrate

β-amyrin

PubChem ↗ [H][C@]12[C@H](O)C=C3[C@]4([H])CC(C)(C)CC[C@]4(C)CC[C@@]3(C)[C@…

CYP716A419

ΔMass: -2.0157 Da ketone_formation(-2.0157)

Product

oleanolic aldehyde

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

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; C28 oxidation step 2 (aldehyde).

Reaction & quality gates

Mechanism: Ketone formation (-2.02 Da)
Evidence type: In vivo
Confidence: High
Data tier: Gold
Latin binomial + experiment + dual SMILES + ΔMass pass
Substrate class: Terpenoids
Product class: Other

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