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Literature summary for 1.14.14.91 extracted from

  • Pfaendler, R.; Scheel, D.; Sandermann, H.; Grisebach, H.
    Stereospecificity of plant microsomal cinnamic acid 4-hydroxylase (1977), Arch. Biochem. Biophys., 178, 315-316.
    View publication on PubMed

Inhibitors

Inhibitors Comment Organism Structure
cis-cinnamate competitive Petroselinum sp.

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
trans-cinnamate + [reduced NADPH-hemoprotein reductase] + O2 Petroselinum sp. enzyme catalyzes an important step in the biosynthesis of flavonoids, lignin and other plant phenolics 4-hydroxycinnamate + [oxidized NADPH-hemoprotein reductase] + H2O
-
?

Organism

Organism UniProt Comment Textmining
Petroselinum sp.
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
cell suspension culture
-
Petroselinum sp.
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
trans-cinnamate + [reduced NADPH-hemoprotein reductase] + O2
-
Petroselinum sp. 4-hydroxycinnamate + [oxidized NADPH-hemoprotein reductase] + H2O
-
?
trans-cinnamate + [reduced NADPH-hemoprotein reductase] + O2 enzyme catalyzes an important step in the biosynthesis of flavonoids, lignin and other plant phenolics Petroselinum sp. 4-hydroxycinnamate + [oxidized NADPH-hemoprotein reductase] + H2O
-
?

Ki Value [mM]

Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
0.34
-
cis-cinnamate
-
Petroselinum sp.