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Results 1 - 9 of 9
EC Number
Natural Substrates
Commentary (Nat. Sub.)
glycine + H-protein-lipoyllysine
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glycine + H-protein-lipoyllysine
P-protein is the actual glycine-decarboxylating enzyme and uses pyridoxal 5'-phosphate as a cofactor. CO2 is released in the reaction and the residual aminomethyl group is bound to the oxidized lipoamide arm of H-protein
glycine + lipoylprotein
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glycine + lipoylprotein
reaction is stimulated by lipoic acid which is a functional group of the H-protein
glycine + lipoylprotein
glycine decarboxylation catalyzed by P-protein alone is extremely low
glycine + lipoylprotein
lipoyl protein: H-protein, lipoamide can also act as acceptor
glycine + [glycine-cleavage complex H protein]-N6-lipoyl-L-lysine
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more
nonketotic hyperglycinaemia is an autosomal recessive disorder of glycine metabolism caused by a deficiency in the mitochondrial glycine cleavage enzyme. The majority of cases are caused by mutations in the P-protein
more
in transgenic potato plants with an antisense reduction in P-protein of GDC, the decrease in photorespiratory decarboxylation is compensated for by an increase in respiratory decarboxylation in the light
Results 1 - 9 of 9