The protein encoded by this gene belongs to a subfamily of the phosphotransferases. This encoded enzyme is responsible for the third and last step in L-serine formation. It catalyzes magnesium-dependent hydrolysis of L-phosphoserine and is also involved in an exchange reaction between L-serine and L-phosphoserine. Deficiency of this protein is thought to be linked to Williams syndrome. [provided by RefSeq, Jul 2008]
Function
calcium ion binding; hydrolase activity; magnesium ion binding; phosphoserine phosphatase activity; phosphoserine phosphatase activity; protein homodimerization activity;
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