3e77 | pdb_00003e77

Human phosphoserine aminotransferase in complex with PLP

spinqualitylabelsall models 3e77, resolution 2.50Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 3e77 is a 3 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 2.5Å Ligands: GOL, PLP Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Disease SERC_HUMAN Defects in PSAT1 are the cause of phosphoserine aminotransferase deficiency (PSATD) [MIM:610992. PSATD is characterized biochemically by low plasma and cerebrospinal fluid concentrations of serine and glycine and clinically by intractable seizures, acquired microcephaly, hypertonia, and psychomotor retardation. Function SERC_HUMAN Catalyzes the reversible conversion of 3-phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4-phosphonooxybutanoate to phosphohydroxythreonine (By similarity). Evolutionary Conservation Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. See Also Phosphoserine aminotransferase

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