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Literature summary for 5.5.1.15 extracted from

  • Eguchi, T.; Dekishima, Y.; Hamano, Y.; Dairi, T.; Seto, H.; Kakinuma, K.
    A new approach for the investigation of isoprenoid biosynthesis featuring pathway switching, deuterium hyperlabeling, and 1H NMR spectroscopy. The reaction mechanism of a novel streptomyces diterpene cyclase (2003), J. Org. Chem., 68, 5433-5438.
    View publication on PubMed

Organism

Organism UniProt Comment Textmining
Streptomyces lividans
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
geranylgeranyl diphosphate the triggering proton is lost at the end of the cyclization reaction Streptomyces lividans terpentedienyl diphosphate
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