2g76
From Proteopedia
Contents |
Crystal structure of human 3-phosphoglycerate dehydrogenase
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.
About this Structure
2g76 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
See Also
Categories: Homo sapiens | Phosphoglycerate dehydrogenase | Arrowsmith, C. | Delft, F von. | Edwards, A. | Gileadi, O. | Oppermann, U. | SGC, Structural Genomics Consortium. | Salah, E. | Savitsky, P. | Sundstrom, M. | Turnbull, A P. | Weigelt, J. | 2-hydroxyacid dehydrogenase | Oxidoreductase | Phosphoglycerate dehydrogenase deficiency | Serine metabolism | Sgc | Structural genomic | Structural genomics consortium
