LBO

Arabidopsis thaliana

Brassicaceae

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

Substrate

methyl carlactonoate

PubChem ↗ COC(=O)C(/C=C/C1=C(C)CCCC1(C)C)=C/O[C@H]1C=C(C)C(=O)O1

LBO

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

1'-hydroxymethyl carlactonoate

PubChem ↗ CC1=C[C@H](O/C=C(\C=C\C2=C(C)CCCC2(C)C)C(=O)OCO)OC1=O

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; LBO converts MeCLA to 1'-HO-MeCLA; confirmed by deuterated feeding experiments.

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: Organic acids
Product class: Organic acids

Literature & public identifiers

PubMed: PMID:32399509 ↗
DOI: 10.1002/pld3.219 ↗
UniProt: Q9LIF4 ↗
GenBank: —
NCBI TaxID: 3702 ↗

Hydroxyl carlactone derivatives are predominant strigolactones in <i>Arabidopsis</i>.

Evidence trail

Reaction & quality gates

Literature & public identifiers

Other reactions by this enzyme