6rj2 | pdb_00006rj2
From Proteopedia
Crystal structure of PHGDH in complex with compound 40
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Structural highlights
Disease[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. Contents | ||||||||||||||||||
This page was last modified 06:06, 7 August 2019.