6plf
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Crystal structure of human PHGDH complexed with Compound 1
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Structural highlights
DiseaseSERA_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. FunctionSee Also | ||||||||||||||||||||
This page was last modified 14:55, 13 March 2024.