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Literature summary extracted from

  • Ullrich, V.; Castle, L.; Weber, P.
    Spectral evidence for the cytochrome P450 nature of prostacyclin synthetase (1981), Biochem. Pharmacol., 30, 2033-2036.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
5.3.99.4 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid
-
 Sus scrofa
5.3.99.4 tranylcypromine
-
 Sus scrofa

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
5.3.99.4 microsome
-
 Sus scrofa
-
-

Organism

EC Number Organism UniProt Comment Textmining
5.3.99.4 Sus scrofa
-
-
-

Reaction

EC Number Reaction Comment Organism Reaction ID
5.3.99.4 (5Z,13E,15S)-9alpha,11alpha-epidioxy-15-hydroxyprosta-5,13-dienoate = (5Z,13E,15S)-6,9alpha-epoxy-11alpha,15-dihydroxyprosta-5,13-dienoate prostaglandin endoperoxyde PGH2 prostacyclin PGI2 , a mechanism with the participation of a heme-thiolate protein is proposed Sus scrofa
a

Source Tissue

EC Number Source Tissue Comment Organism Textmining
5.3.99.4 aorta
-
 Sus scrofa
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
5.3.99.4 Prostaglandin H2
-
 Sus scrofa Prostaglandin I2 prostaglandin I2 ?