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Results 1 - 10 of 11 > >>
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31(+)-alpha-pinene + NADPH + H+ + O2 - Ips pini verbenol + NADP+ + H2O - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31(-)-alpha-pinene + NADPH + H+ + O2 - Ips pini cis-verbenol + NADP+ + H2O - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31(-)-alpha-pinene + NADPH + H+ + O2 - Ips pini myrtenol + NADP+ + H2O - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.313-carene + NADPH + H+ + O2 - Ips pini ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31more no activity with alpha-phellandrene, (-)-beta-pinene, gamma-terpinene, or terpinolene Ips pini ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31more no activity with amitinol, E-myrcenol, linalool or geraniol Ips pini ? - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31myrcene + NADPH + H+ + O2 myrcene is 7-methyl-3-methylene-1,6-octadiene Ips pini (4R)-(-)-ipsdienol + NADP+ + H2O 81% yield, ipsidenol is 2-methyl-6-methylene-2,7-octadien-4-ol ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31myrcene + NADPH + H+ + O2 - Ips confusus (R)-ipsdienol + NADP+ + H2O 85% yield ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31myrcene + NADPH + H+ + O2 87% yield of (-)-ipsdienol, 13% yield of (+)-ipsdienol Ips pini ipsdienol + NADP+ + H2O - ?
Display the word mapDisplay the reaction diagram Show all sequences 1.14.14.31myrcene + NADPH + H+ + O2 the enzyme strongly prefers myrcene over other substrates Ips pini ipsdienol + NADP+ + H2O 80% yield of (-)-ipsdienol, 20% yield of (+)-ipsdienol ?
Results 1 - 10 of 11 > >>