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GLDC, glycine decarboxylase

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GLDC, glycine decarboxylase

  • Degradation of glycine is brought about by the glycine cleavage system, which is composed of four mitochondrial protein components: P protein (a pyridoxal phosphate-dependent glycine decarboxylase), H protein (a lipoic acid-containing protein), T protein (a tetrahydrofolate-requiring enzyme), and L protein (a lipoamide dehydrogenase). The protein encoded by this gene is the P protein, which binds to glycine and enables the methylamine group from glycine to be transferred to the T protein. Defects in this gene are a cause of nonketotic hyperglycinemia (NKH).[provided by RefSeq, Jan 2010]

  • Gene Synonyms (glycine dehydrogenase (decarboxylating), mitochondrial, glycine cleavage system protein P, glycine decarboxylase P-protein, glycine dehydrogenase (aminomethyl-transferring), glycine dehydrogenase [decarboxylating], mitochondrial, nonketotic hyperglycinemia, GCE, GCSP, HYGN1,)
  • NCBI Gene ID: 2731
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>P23378
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

glycine decarboxylase interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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