5n6c, resolution 2.30Å
[SERA_HUMAN] Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency (PHGDH deficiency) [MIM:601815]. It is characterized by congenital microcephaly, psychomotor retardation, and seizures.
OCA
Categories: Phosphoglycerate dehydrogenase | Basle, A | Cano, C | Curtin, N J | Noble, M E.M | Tucker, J | Unterlass, J E | Dehydrogenase | Enzymology | Oxidoreductase | Serine metabolism