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Literature summary 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

EC Number Organism UniProt Comment Textmining
4.2.3.116 Salvia officinalis
-
-
-
4.2.3.117 Salvia officinalis
-
-
-
4.2.3.119 Salvia officinalis
-
-
-
4.2.3.120 Salvia officinalis
-
-
-
4.2.3.121 Salvia officinalis
-
-
-
4.2.3.122 Salvia officinalis
-
isoform cyclase III
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4.2.3.116 geranyl diphosphate
-
Salvia officinalis (+)-camphene + diphosphate products are (+)-alpha-pinene and (+)-camphene ?
4.2.3.116 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 ?
-
?
4.2.3.117 geranyl diphosphate
-
Salvia officinalis (-)-camphene + diphosphate products are (-)-alpha-pinene, (-)-beta-pinene, and (-)-camphene ?
4.2.3.117 additional information enzymes removes the C4-proS-hydrogen of the substrate, the C3 proton of the corresponding pinyl cation, with a stereoselectivity exceeding 78% in the formation of (-)-alpha-pinene Salvia officinalis ?
-
?
4.2.3.119 geranyl diphosphate
-
Salvia officinalis (-)-alpha-pinene + diphosphate products are (-)-alpha-pinene, (-)-beta-pinene, and (-)-camphene ?
4.2.3.119 additional information enzymes removes the C4-proS-hydrogen of the substrate, the C3 proton of the corresponding pinyl cation, with a stereoselectivity exceeding 78% in the formation of (-)-alpha-pinene Salvia officinalis ?
-
?
4.2.3.120 geranyl diphosphate
-
Salvia officinalis (-)-beta-pinene + diphosphate products are (-)-alpha-pinene, (-)-beta-pinene, and (-)-camphene ?
4.2.3.120 additional information enzymes removes the C4-proS-hydrogen of the substrate, the C3 proton of the corresponding pinyl cation, with a stereoselectivity exceeding 78% in the formation of (-)-alpha-pinene Salvia officinalis ?
-
?
4.2.3.121 geranyl diphosphate
-
Salvia officinalis (+)-alpha-pinene + diphosphate products of cyclase I are (+)-alpha-pinene and (+)-camphene, products of cyclase III are (+)-alpha-pinene and (+)-beta-pinene ?
4.2.3.121 additional information enzymes 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 ?
-
?
4.2.3.122 geranyl diphosphate
-
Salvia officinalis (+)-beta-pinene + diphosphate products are (+)-alpha-pinene and (+)-beta-pinene ?
4.2.3.122 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

EC Number Synonyms Comment Organism
4.2.3.117 cyclase II
-
Salvia officinalis
4.2.3.119 cyclase II
-
Salvia officinalis
4.2.3.120 cyclase II
-
Salvia officinalis
4.2.3.121 cyclase I
-
Salvia officinalis
4.2.3.121 cyclase III
-
Salvia officinalis
4.2.3.122 cyclase III
-
Salvia officinalis