2g76 | pdb_00002g76
From Proteopedia
Crystal structure of human 3-phosphoglycerate dehydrogenase
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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. Evolutionary ConservationCheck, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. See Also | ||||||||||||||||||||||
This page was last modified 18:49, 10 March 2021.