CYP75A

Solanum melongena CYP75A

Solanaceae

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

Substrate

dihydrokaempferol

PubChem ↗ C1=CC(=CC=C1[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O)O

CYP75A

ΔMass: +15.9949 Da hydroxylation(+15.9949)

Product

dihydroquercetin

PubChem ↗ C1=CC(=C(C=C1[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O)O)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; Inferred from transcriptome and metabolome co-analysis; gene expression correlated with anthocyanin accumulation; no direct enzyme assay.

Reaction & quality gates

Mechanism: Hydroxylation (+15.99 Da)
Evidence type: In vivo
Confidence: High
Data tier: Quarantine
PDF audit quarantine (enzyme_miss_in_pdf;weak_text_core;review_text_weak_core). pdf=39511492.pdf; enzyme_in_pdf=miss; issue=review_text_weak_core; core=weak_te…
Substrate class: Phenylpropanoids
Product class: Phenylpropanoids

Literature & public identifiers

PubMed: PMID:39511492 ↗
DOI: 10.1186/s12864-024-10990-z ↗
UniProt: —
GenBank: —
NCBI TaxID: 4111 ↗

Genome-wide identification and functional analysis of CYP450 genes in eggplant (Solanum melongena L.) with a focus on anthocyanin accumlation.