CYP98A3

The reaction CYP98A

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

Substrate

coumaroyl esters

PubChem ↗ Crowdsource substrate structure

CYP98A3

ΔMass: no_smiles Missing dual SMILES or RDKit not validated

Product

3'-hydroxycoumaroyl esters

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; CYP98A3 is described as a coumaroyl esters 3'-hydroxylase involved in lignin monomer synthesis. The reaction is inferred from functional characterization in the literature (refs 23-25).

Reaction & quality gates

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

Literature & public identifiers

PubMed: PMID:12153706 ↗
DOI: 10.1186/1471-2229-2-7 ↗
UniProt: A0A5P8H637 ↗
GenBank: —
NCBI TaxID: —

Conservation and diversity of gene families explored using the CODEHOP strategy in higher plants.