MAX1

Arabidopsis thaliana

Brassicaceae

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

Substrate

carlactone

PubChem ↗ CC1=C(C(CCC1)(C)C)/C=C/C(=C\OC2C=C(C(=O)O2)C)/C

MAX1

ΔMass: +29.9742 Da methyl_to_carboxyl(+29.9742)

Product

carlactonoic acid

PubChem ↗ CC1=CC(O/C=C(\C=C\C2=C(C)CCCC2(C)C)/C(=O)O)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; Recombinant MAX1 expressed in yeast converts CL to CLA (Abe et al., 2014).

Reaction & quality gates

Mechanism: Oxidation
Evidence type: In vitro
Confidence: High
Data tier: Gold
Latin binomial + experiment + dual SMILES + ΔMass pass
Substrate class: Other
Product class: Organic acids

Literature & public identifiers

PubMed: PMID:32399509 ↗
DOI: 10.1002/pld3.219 ↗
UniProt: A5YYJ7 ↗
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