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Results 1 - 8 of 8
EC Number Natural Substrates Commentary (Nat. Sub.)
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127(3S)-linalool -
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127(3S)-linalool LinD enantioselectively transforms beta-myrcene to (S)-(+)-linalool (coriandrol) with an enantiomeric excess of at least 95.4%
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127(R,S)-linalool -
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127beta-myrcene + H2O -
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127more the bifunctional linalool dehydratase isomerase (LinD) catalyzes the isomerization of geraniol to linalool, EC 5.4.4.4, and likewise the dehydration of linalool to myrcene, EC 4.2.1.127
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127more the bifunctional linalool dehydratase isomerase (LinD) catalyzes the isomerization of geraniol to linalool, EC 5.4.4.4, and likewise the dehydration of linalool to myrcene, EC 4.2.1.127. No activity with alpha-ocimene and beta-ocimene as well as citronellol and nerol. LinD accepts a broad variety of elongated and truncated aliphatic and even aromatic tertiary alcohols (C5-C15) providing chiral dehydration products with selectivity factors of up to 200. Substrates lacking the signature motif are not accepted by LinD
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127more the bifunctional linalool dehydratase isomerase (LinD)catalyzes the isomerization of geraniol to linalool, EC 5.4.4.4, and likewise the dehydration of linalool to beta-myrcene, EC 4.2.1.127
Display the word mapDisplay the reaction diagram Show all sequences 4.2.1.127myrcene + H2O degradation of myrcene
Results 1 - 8 of 8