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Literature summary extracted from

  • Hashim, M.F.; Hakamatsuka, T.; Ebizuka, Y.; Sankawa, U.
    Reaction mechanism of oxidative rearrangement of flavanone in isoflavone biosynthesis (1990), FEBS Lett., 271, 219-22.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
1.14.14.87 Ancymidol complete inhibition at 1 mM Pueraria montana var. lobata
1.14.14.87 CO2 52% inhibition in the presence of CO2 gas Pueraria montana var. lobata
1.14.14.87 Metyrapone complete inhibition at 0.1 mM Pueraria montana var. lobata
1.14.14.87 SKF 525-A 73% inhibition at 2 mM Pueraria montana var. lobata
1.14.14.87 uniconazole complete inhibition at 0.1 mM Pueraria montana var. lobata

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
1.14.14.87 microsome
-
Pueraria montana var. lobata
-
-

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
1.14.14.87 Iron the (P450) enzyme contains iron Pueraria montana var. lobata

Organism

EC Number Organism UniProt Comment Textmining
1.14.14.87 Pueraria montana var. lobata
-
-
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
1.14.14.87 liquiritigenin + [reduced NADPH-hemoprotein reductase] + O2
-
Pueraria montana var. lobata 2,7,4'-trihydroxyisoflavanone + [oxidized NADPH-hemoprotein reductase] + H2O major product is 2,7,4'-trihydroxyisoflavanone which further reacts to daidzein ?

Synonyms

EC Number Synonyms Comment Organism
1.14.14.87 CYT93C
-
Pueraria montana var. lobata
1.14.14.87 IFS
-
Pueraria montana var. lobata