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Literature summary extracted from

  • Kushiro, T.; Hoshino, M.; Tsutsumi, T.; Kawai, K.i.; Shiro, M.; Shibuya, M.; Ebizuka, Y.
    Stereochemical course in water addition during LUP1-catalyzed triterpene cyclization (2006), Org. Lett., 8, 5589-5592.
    View publication on PubMed

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
4.2.1.128 (3S)-2,3-epoxy-2,3-dihydrosqualene + H2O Arabidopsis thaliana
-
lupan-3beta,20-diol
-
?

Organism

EC Number Organism UniProt Comment Textmining
4.2.1.128 Arabidopsis thaliana Q9C5M3
-
-
5.4.99.41 Arabidopsis thaliana
-
isoform LUP1
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4.2.1.128 (3S)-2,3-epoxy-2,3-dihydrosqualene + H2O
-
Arabidopsis thaliana lupan-3beta,20-diol
-
?
5.4.99.41 2,3-oxidosqualene
-
Arabidopsis thaliana lupeol enzyme additionally catalyzes the stereospecific addition of water to yield 3beta,20-dihydroxylupane without rotation of the C19-C20 bond ?

Synonyms

EC Number Synonyms Comment Organism
4.2.1.128 At1g78970
-
Arabidopsis thaliana
4.2.1.128 LUP1
-
Arabidopsis thaliana