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5.3.99.4: prostaglandin-I synthase

This is an abbreviated version!
For detailed information about prostaglandin-I synthase, go to the full flat file.

Word Map on EC 5.3.99.4

Reaction

(5Z,13E,15S)-9alpha,11alpha-epidioxy-15-hydroxyprosta-5,13-dienoate
=
(5Z,13E,15S)-6,9alpha-epoxy-11alpha,15-dihydroxyprosta-5,13-dienoate

Synonyms

Aortic cytochrom P450, CYP8A1, PGI synthase, PGI2 synthase, PGI2 synthetase, PGI2-S, PGIS, prostacyclin synthase, Prostacyclin synthetase, prostacyclin-synthase, prostacyclin/PGI2 synthase, Prostacycline synthetase, prostaglandin I synthase, Prostaglandin I2 synthase, Prostaglandin I2 synthetase, Ptgis, Synthetase, prostacyclin

ECTree

     5 Isomerases
         5.3 Intramolecular oxidoreductases
             5.3.99 Other intramolecular oxidoreductases
                5.3.99.4 prostaglandin-I synthase

Oxidation Stability

Oxidation Stability on EC 5.3.99.4 - prostaglandin-I synthase

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OXIDATION STABILITY
ORGANISM
UNIPROT
LITERATURE
destructive action of a nascent oxidizing agent released from prostaglandin G1, 15-hydroperoxy-prostaglandin E1, 15-hydroperoxy-5,8,11,13-eicosatetraenoic acid, and 12-hydroxy-5,8,10,14-eicosatetraenoic acid is prevented by 2-aminomethyl-4-tert-6-iodophenol
-
37459
human PGIS is significantly unstable when the heme cofactor appears in the reduction and/or reduction-CO binding state
-
662059
the prostacyclin synthase is unusually sensitive to the redox state or sulfhydryl oxidation of the enzyme
-
3127