PDB ID 6rj5
[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: Large Structures | Bader, G | Wolkerstorfer, B | Zoephel, A | Dehydrogenase | Oxidoreductase | Protein-ligand complex