Bronze
no_smiles
Hydroxylation
Substrate reaction site
Product reaction site
MCS substructure diff highlighting · RDKit atom mapping
CYP98A3
ΔMass: no_smiles
Missing dual SMILES or RDKit not validated
Product
caffeoyl shikimic acid
PubChem ↗
O=C(/C=C/c1ccc(O)c(O)c1)O[C@@H]1CC(C(=O)O)=C[C@@H](O)[C@H]1O
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 also catalyzes the hydroxylation of p-coumaroyl shikimic acid to caffeoyl shikimic acid. The paper mentions this activity, but no direct enzyme assay is provided.
Reaction & quality gates
- Mechanism
- Hydroxylation
- Evidence type
- Pathway_inference
- Confidence
- Medium
- Data tier
- Bronze
evidence=Pathway_inference - Substrate class
- Organic acids
- Product class
- Organic acids
Literature & public identifiers
- PubMed
- PMID:36209069 ↗
- DOI
- 10.1186/s12864-022-08921-x ↗
- UniProt
- A0A5P8H637 ↗
- GenBank
- —
- NCBI TaxID
- 161397 ↗
De novo full length transcriptome analysis and gene expression profiling to identify genes involved in phenylethanol glycosides biosynthesis in Cistanche tubulosa.