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UDP - acetylglucosamine

Fig. 22.8. Coarse facial features and progressive mental retardation are characteristic symptoms in both, sialic storage disorder and sialuria. Differentiation is possible only by measuring UDP-acetylglucosamine 2-epimerase, that is mutated in sialuria... Fig. 22.8. Coarse facial features and progressive mental retardation are characteristic symptoms in both, sialic storage disorder and sialuria. Differentiation is possible only by measuring UDP-acetylglucosamine 2-epimerase, that is mutated in sialuria...
Stable and potent P2Y2 receptor agonists are being administered by inhalation as a potential treatment for cystic fibrosis. P2YH receptors are unusual in that they are activated by UDP-glucose, UDP galactose and UDP-N-acetylglucosamine [22],... [Pg.315]

Raetz, C. R., and Roderick, S. L. (1995). A left-handed parallel beta helix in the structure of UDP-N-acetylglucosamine acyl transferase. Science 270, 997-1000. [Pg.95]

This enzyme [EC 2.4.1.22] is a protein complex of two proteins (designated A and B) and catalyzes the reaction of UDP-galactose with D-glucose to generate UDP and lactose. In the absence of the ce-lactalbumin (protein B), the enzyme catalyzes the transfer of galactose from UDP-galactose to A-acetylglucosamine (Le., the activity of A-acetyllactosamine synthase, EC 2.4.1.90). [Pg.414]

Enzyme preparations pretreated by dialysis at pH 9.2 (dialysis) or with digitonin (digitonin), or UDP-JV-acetylglucosamine (UDPNAGA) added to enzymatic incubation mixtures. [Pg.243]

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See also in sourсe #XX -- [ Pg.9 ]



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