Cat.No.: | PSPH-1430HCL |
Description: | 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. |
Species: | Human |
Size: | 100 ul |
Storage Buffer: | 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue) |
Applications: | Western Blot; |
Gene Name: | PSPH phosphoserine phosphatase [ Homo sapiens ] |
Official Symbol: | PSPH |
Synonyms: | PSPH; phosphoserine phosphatase; PSP; PSPase; L-3-phosphoserine phosphatase; O-phosphoserine phosphohydrolase; PSPHD; |
Gene ID: | 5723 |
mRNA Refseq: | NM_004577 |
Protein Refseq: | NP_004568 |
MIM: | 172480 |
UniProt ID: | P78330 |
Chromosome Location: | 7p11.2 |
Pathway: | Amino acid synthesis and interconversion (transamination), organism-specific biosystem; Glycine, serine and threonine metabolism, organism-specific biosystem; Glycine, serine and threonine metabolism, conserved biosystem; Metabolic pathways, organism-specific biosystem; Metabolism, organism-specific biosystem; Metabolism of amino acids and derivatives, organism-specific biosystem; Serine biosynthesis, organism-specific biosystem; |
Function: | calcium ion binding; hydrolase activity; magnesium ion binding; phosphoserine phosphatase activity; phosphoserine phosphatase activity; protein homodimerization activity; |
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