Glutamate dehydrogenase substrate site

An understanding of the molecular basis for regulation of isocitrate dehydrogenase by phosphorylation was facilitated by X-ray crystallography of the phosphorylated enzyme in complex with isocitrate. The crystal structures of mutants of the enzyme in which SerllS had been exchanged for aspartate or glutamate were also solved (Hurley et al., 1990). The structure of the enzyme in complex with the substrate isocitrate revealed the phophorylation site to be localized near isocitrate. SerllS itself binds the substrate directly via a H-bond with the O of isocitrate (fig. 2.13). 

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