CYP76M8

Oryza sativa CYP76M

Poaceae

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

Substrate

3α-Hydroxy-ent-sandaracopimaradiene

PubChem ↗ C[C@]1(CC[C@@H]2C(=C1)CC[C@H]3[C@]2(CC[C@H](C3(C)C)O)C)C=C

CYP76M8

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

oryzalexin D

PubChem ↗ C[C@]1(CC[C@@H]2C(=C1)[C@H](C[C@H]3[C@]2(CC[C@H](C3(C)C)O)C)O)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; CYP76M8 hydroxylates C-7β position leading to oryzalexin D; reference [78].

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vitro
Confidence: High
Data tier: Gold
Latin binomial + experiment + dual SMILES + ΔMass pass
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:39329985 ↗
DOI: 10.3390/cimb46090634 ↗
UniProt: Q6YTF1 ↗
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