ElADH1

Euphorbia lathyris

Euphorbiaceae

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

Substrate

9-hydroxycasbene

PubChem ↗ C/C/1=C\CC(/C(=C/CC/C(=C/[C@@H]2[C@@H](C2(C)C)CC1)/C)/C)O

ElADH1

ΔMass: -2.0157 Da ketone_formation(-2.0157)

Product

9-ketocasbene

PubChem ↗ C/C/1=C\CC(=O)/C(=C/CC/C(=C/[C@@H]2[C@@H](C2(C)C)CC1)/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; ADH1 catalyzes dehydrogenation of 9-hydroxyl group of 9-hydroxycasbene to form 9-ketocasbene; confirmed by in vitro enzyme assays.

Reaction & quality gates

Mechanism: Ketone formation (-2.02 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:27506796 ↗
DOI: 10.1073/pnas.1607504113 ↗
UniProt: KR350665 ↗
GenBank: KR350665 ↗
NCBI TaxID: 212925 ↗

Oxidation and cyclization of casbene in the biosynthesis of Euphorbia factors from mature seeds of Euphorbia lathyris L.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme