6plf | pdb_00006plf
From Proteopedia
Crystal structure of human PHGDH complexed with Compound 1
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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 06:26, 24 July 2019.