CYP82G1

Arabidopsis thaliana

Brassicaceae

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

Substrate

(E)-nerolidol

PubChem ↗ CC(=CCC/C(=C/CCC(C)(C=C)O)/C)C

CYP82G1

ΔMass: -72.0575 Da mismatch

Product

(E)-4,8-dimethyl-1,3,7-nonatriene (DMNT)

PubChem ↗ CC(=CCC/C(=C/C=C)/C)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; 转化酵母WAT11细胞体内酶活测定，顶空SPME-GC-MS检测产物。

Reaction & quality gates

Mechanism: Oxidation
Evidence type: In vivo
Confidence: High
Data tier: Silver
mass=mismatch
Substrate class: Other
Product class: Other

Literature & public identifiers

PubMed: PMID:21088219 ↗
DOI: 10.1073/pnas.1009975107 ↗
UniProt: Q9LSF8 ↗
GenBank: —
NCBI TaxID: 3702 ↗

Herbivore-induced and floral homoterpene volatiles are biosynthesized by a single P450 enzyme (CYP82G1) in Arabidopsis.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme