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Results 1 - 6 of 6
EC Number Reaction Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.19ent-copalyl diphosphate = ent-kaurene + diphosphate - -
Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.19ent-copalyl diphosphate = ent-kaurene + diphosphate cyclization mechanism catalyzed by KSs and the Ile mutants, via ent-pimar-15-en-8-yl, ent-beyeran-16-yl, and ent-kauran-16-yl intermediates, detailed overview 747870
Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.19ent-copalyl diphosphate = ent-kaurene + diphosphate cyclization mechanism derived from quantum chemical calculation for the formation of ent-kaurene and related diterpenes, overview 748876
Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.19ent-copalyl diphosphate = ent-kaurene + diphosphate reaction mechanism, overview -, 749301
Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.19ent-copalyl diphosphate = ent-kaurene + diphosphate the determination of the final products of CPS/KSs in bryophytes depends on the sequence and structure of the C-terminal regions of CPS/KSs. Thus, the type A cyclization reaction of both PpCPS/KS and JsCPS /KS occurs near the C-terminal region of the polypeptides 714971
Display the word mapDisplay the reaction diagram Show all sequences 4.2.3.19ent-copalyl diphosphate = ent-kaurene + diphosphate the hydrophobicity and size of the side chain residue at the bifunctional CPS/KS amino acid 710 is responsible for quenching the ent-kauranyl cation by the addition of a water molecule. The determination of the final products of CPS/KSs in bryophytes depends on the sequence and structure of the C-terminal regions of CPS/KSs. Thus, the type A cyclization reaction of both PpCPS/KS and JsCPS /KS occurs near the C-terminal region of the polypeptides 714971
Results 1 - 6 of 6