cpath:CPATH-149532 | rdf:type | http://www.biopax.org/relea... | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-618391 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-618392 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-618393 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-618394 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-618395 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-626670 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | Glycine dehydrogenase [decarboxylating], mitochondrial | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | GCSP_HUMAN | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | cpath:CPATH-LOCAL-618389 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | 1.4.4.2 | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | Glycine decarboxylase | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | Glycine cleavage system P protein | lld:biogrid |
cpath:CPATH-149532 | http://www.biopax.org/relea... | FUNCTION: The glycine cleavage system catalyzes the degradation of glycine. The P protein binds the alpha-amino group of glycine through its pyridoxal phosphate cofactor; CO(2) is released and the remaining methylamine moiety is then transferred to the lipoamide cofactor of the H protein. CATALYTIC ACTIVITY: Glycine + H-protein-lipoyllysine = H-protein- S-aminomethyldihydrolipoyllysine + CO(2). COFACTOR: Pyridoxal phosphate. SUBUNIT: Homodimer. The glycine cleavage system is composed of four proteins: P, T, L and H. SUBCELLULAR LOCATION: Mitochondrion. DISEASE: Defects in GLDC are a cause of non-ketotic hyperglycinemia (NKH) [MIM:605899]; also known as glycine encephalopathy (GCE). NKH is an autosomal recessive disease characterized by accumulation of a large amount of glycine in body fluid and by severe neurological symptoms. SIMILARITY: Belongs to the gcvP family. WEB RESOURCE: Name=GeneReviews; URL="http://www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/GLDC"; GENE SYNONYMS: GCSP. COPYRIGHT: Protein annotation is derived from the UniProt Consortium (http://www.uniprot.org/). Distributed under the Creative Commons Attribution-NoDerivs License. | lld:biogrid |
cpath:CPATH-149532 | skos:exactMatch | uniprot-protein:P23378 | lld:mappings |
cpath:CPATH-149532 | skos:closeMatch | entrez-gene:2731 | lld:mappings |
cpath:CPATH-LOCAL-11349144 | http://www.biopax.org/relea... | cpath:CPATH-149532 | lld:biogrid |
cpath:CPATH-LOCAL-11349145 | http://www.biopax.org/relea... | cpath:CPATH-149532 | lld:biogrid |
cpath:CPATH-LOCAL-11461614 | http://www.biopax.org/relea... | cpath:CPATH-149532 | lld:biogrid |