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Silver no_smiles Hydroxylation

CYP711A3

Oryza sativa

Poaceae

Substrate reaction site Product reaction site MCS substructure diff highlighting · RDKit atom mapping
Substrate
methyl 4-oxo-carlactonoate
PubChem ↗ Crowdsource substrate structure
CYP711A3
ΔMass: no_smiles Missing dual SMILES or RDKit not validated
Product
18-OH-4-oxo-MeCLA
PubChem ↗ Crowdsource product structure

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; PMID 39297385: In vitro assay with yeast microsomes expressing OsMAX1-1400; 4-oxo-MeCLA conversion to OH-4-oxo-MeCLA (tentatively 18-OH) confirmed by LC-MS/MS.

Reaction & quality gates

Mechanism
Hydroxylation
Evidence type
In vitro
Confidence
High
Data tier
Silver
mass=no_smiles; incomplete_SMILES
Substrate class
Organic acids
Product class
Other

Literature & public identifiers

PubMed
PMID:39297385 ↗
DOI
10.1111/nph.20135 ↗
UniProt
A0A809PWT0 ↗
GenBank
NCBI TaxID
4530 ↗

The rice orobanchol synthase catalyzes the hydroxylation of the noncanonical strigolactone methyl 4-oxo-carlactonoate.