OBH

Conversion rate CYP98A

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

Substrate

p-coumaroylquinic acid

PubChem ↗ C1[C@@H]([C@@H]([C@H](C[C@]1(C(=O)O)O)OC(=O)/C=C/C2=CC=C(C=C2)O…

OBH

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

chlorogenic acid

PubChem ↗ C1[C@H]([C@H]([C@@H](C[C@@]1(C(=O)O)O)OC(=O)/C=C/C2=CC(=C(C=C2)…

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; Conversion rate <5%; OBHs show low activity on p-coumaroylquinic acid.

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vitro
Confidence: Low
Data tier: Quarantine
non-CYP auxiliary enzyme (pathway partner, not cytochrome P450)
Substrate class: Organic acids
Product class: Organic acids

Literature & public identifiers

PubMed: PMID:36935606 ↗
DOI: 10.1016/j.xplc.2023.100592 ↗
UniProt: —
GenBank: —
NCBI TaxID: —

Complete biosynthesis of the phenylethanoid glycoside verbascoside.