CYP99A3

Oryza sativa CYP99A

Poaceae

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

Substrate

syn-stemar-13-ene

PubChem ↗ CC1=C[C@@H]2CC[C@@H]3[C@@]([C@@]24CC[C@@H]1C4)(CCCC3(C)C)C

CYP99A3

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

syn-stemar-13-en-19-ol

PubChem ↗ Crowdsource product structure

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; CYP99A3 and CYP99A2 hydroxylate C19 of syn-stemar-13-ene; reference [82].

Reaction & quality gates

Mechanism: Hydroxylation
Evidence type: In vitro
Confidence: High
Data tier: Silver
mass=no_smiles; incomplete_SMILES
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:39329985 ↗
DOI: 10.3390/cimb46090634 ↗
UniProt: Q0JF01 ↗
GenBank: —
NCBI TaxID: 4530 ↗

Enhancing Crop Resilience: Insights from Labdane-Related Diterpenoid Phytoalexin Research in Rice (<i>Oryza sativa</i> L.).

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme