NP_058662.2
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
56,586 Da
NCBI Official Full Name
D-3-phosphoglycerate dehydrogenase
NCBI Official Synonym Full Names
3-phosphoglycerate dehydrogenase
NCBI Official Synonym Symbols
A10; PGD; PGAD; PGDH; SERA; 3PGDH; 3-PGDH; 4930479N23 [Similar Products]
NCBI Protein Information
D-3-phosphoglycerate dehydrogenase
UniProt Protein Name
D-3-phosphoglycerate dehydrogenase
UniProt Synonym Protein Names
A10
UniProt Synonym Gene Names
UniProt Entry Name
SERA_MOUSE
UniProt Comments for Phgdh
PHGDH: Defects in PHGDH are the cause of phosphoglycerate dehydrogenase deficiency (PHGDH deficiency). It is characterized by congenital microcephaly, psychomotor retardation, and seizures. Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family.
Protein type: Amino Acid Metabolism - glycine, serine and threonine; Oxidoreductase; EC 1.1.1.95; Cell development/differentiation
Cellular Component: myelin sheath
Molecular Function: NAD binding; oxidoreductase activity; oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor; phosphoglycerate dehydrogenase activity
Biological Process: amino acid biosynthetic process; gamma-aminobutyric acid metabolic process; glial cell development; glutamine metabolic process; glycine metabolic process; L-serine biosynthetic process; L-serine metabolic process; metabolic process; neural tube development; neurite development; neurogenesis; regulation of gene expression; serine family amino acid biosynthetic process; spinal cord development; taurine metabolic process; threonine metabolic process
Research Articles on Phgdh
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Products associated with Phgdh elisa kit
Pathways associated with Phgdh elisa kit
Diseases associated with Phgdh elisa kit
Organs/Tissues associated with Phgdh elisa kit
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