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Chalcone O-methyltransferase

ARCHITECTURE OF TYPE 1 O-METHYLTRANSFERASES Chalcone O-Methyltransferase (ChOMT)... [Pg.44]

The understanding of the degradation of natural products such as camphor has been greatly enhanced by understanding the catalytic cycle of the cytochrome P-450 enzyme P-450cam in structural detail.3,4 These enzymes catalyze the addition of 02 to nonactivated hydrocarbons at room temperatures and pressures - a reaction that requires high temperature to proceed in the absence of a catalyst. O-Methyltransferases are central to the secondary metabolic pathway of phenylpropanoid biosynthesis. The structural basis of the diverse substrate specificities of such enzymes has been studied by solving the crystal structures of chalcone O-methyltransferase and isoflavone O-methyltransferase complexed with the reaction products.5 Structures of these and other enzymes are obviously important for the development of biomimetic and thus environmentally more friendly approaches to natural product synthesis. [Pg.52]

Fig. 4 Architecture of the chalcone O-methyltransferase isoflavone (a) and O-methyltransferase (lOMT) (b) active sites. Structural analysis shows that the tertiary structures of these enzymes are highly conserved substrate selectivity is determined by variations in side chains on the active site surface that alter van der Walls interactions and hydrogen bonding patterns (From [32])... Fig. 4 Architecture of the chalcone O-methyltransferase isoflavone (a) and O-methyltransferase (lOMT) (b) active sites. Structural analysis shows that the tertiary structures of these enzymes are highly conserved substrate selectivity is determined by variations in side chains on the active site surface that alter van der Walls interactions and hydrogen bonding patterns (From [32])...
Figure 6.1 Major branch pathways of flavonoid biosynthesis in Arabidopsis. Branch pathways, enzymes, and end products present in other plants but not Arabidopsis are shown in light gray. Abbreviations cinnamate-4-hydroxylase (C4H), chalcone isomerase (CHI), chalcone synthase (CHS), 4-coumarate CoA-ligase (4CL), dihydroflavonol 4-reductase (DFR), flavanone 3-hydroxylase (F3H), flavonoid 3 or 3 5 hydroxylase (F3 H, F3 5 H), leucoanthocyanidin dioxygenase (LDOX), leucoanthocyanidin reductase (LCR), O-methyltransferase (OMT), phenylalanine ammonia-lyase (PAL), rhamnosyl transferase (RT), and UDP flavonoid glucosyl transferase (UFGT). Figure 6.1 Major branch pathways of flavonoid biosynthesis in Arabidopsis. Branch pathways, enzymes, and end products present in other plants but not Arabidopsis are shown in light gray. Abbreviations cinnamate-4-hydroxylase (C4H), chalcone isomerase (CHI), chalcone synthase (CHS), 4-coumarate CoA-ligase (4CL), dihydroflavonol 4-reductase (DFR), flavanone 3-hydroxylase (F3H), flavonoid 3 or 3 5 hydroxylase (F3 H, F3 5 H), leucoanthocyanidin dioxygenase (LDOX), leucoanthocyanidin reductase (LCR), O-methyltransferase (OMT), phenylalanine ammonia-lyase (PAL), rhamnosyl transferase (RT), and UDP flavonoid glucosyl transferase (UFGT).

See other pages where Chalcone O-methyltransferase is mentioned: [Pg.37]    [Pg.1102]    [Pg.37]    [Pg.1102]    [Pg.48]    [Pg.172]    [Pg.164]    [Pg.1572]    [Pg.1858]   


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