5n6c | pdb_00005n6c
From Proteopedia
Crystal structure of human 3-phosphoglycerate dehydrogenase in complex with NAD and L-Tartrate
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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 07:37, 22 November 2017.