Any feedback?
Please rate this page
(literature.php)
(0/150)

BRENDA support

Literature summary for 4.2.3.122 extracted from

  • Pyun, H.J.; Wagschal, K.C.; Jung, D.; Coates, R.M.; Croteau, R.
    Stereochemistry of the proton elimination in the formation of (+)- and (-)-alpha-pinene by monoterpene cyclases from sage (Salvia officinalis) (1994), Arch. Biochem. Biophys., 308, 488-496.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Salvia officinalis
-
isoform cyclase III
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
geranyl diphosphate
-
Salvia officinalis (+)-beta-pinene + diphosphate products are (+)-alpha-pinene and (+)-beta-pinene ?
additional information enzyme removes the C4-proR-hydrogen of the substrate, the C3 proton trans to the dimethyl bridge of the pinyl nucleus, with a stereoselectivity exceeding 94% in the formation of (+)-alpha-pinene Salvia officinalis ?
-
?

Synonyms

Synonyms Comment Organism
cyclase III
-
Salvia officinalis