6q6j | pdb_00006q6j
From Proteopedia
Human phosphoserine phosphatase with substrate analogue homo-cysteic acid
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Structural highlights
Disease[SERB_HUMAN] Defects in PSPH are the cause of phosphoserine phosphatase deficiency (PSPHD)[MIM:614023]. A disorder that results in pre- and postnatal growth retardation, moderate psychomotor retardation and facial features suggestive of Williams syndrome.[1] Function[SERB_HUMAN] Catalyzes the last step in the biosynthesis of serine from carbohydrates. The reaction mechanism proceeds via the formation of a phosphoryl-enzyme intermediates.[2] References
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This page was last modified 05:45, 12 June 2019.