Glucose 6 phosphate isomerase è un gene codificato dal simbolo GPI. Comunemente indicato anche come: Glucose-6-phosphate isomerase; GPI; Autocrine motility factor; AMF; Neuroleukin; NLK; Phosphoglucose isomerase; PGI; Phosphohexose isomerase; PHI; Sperm antigen 36; SA-36. Glucose 6 phosphate isomerase ha una massa di 63.15kDa, una lunghezza di amminoacidi di 558, ed è implicato in Hemolytic anemia, non-spherocytic, due to glucose phosphate isomerase deficiency.
Offriamo 7 anticorpi contro Glucose 6 phosphate isomerase, allevati nel Coniglio e Topo, che sono adatti per WB, IHC, ELISA, ICC/IF e Dot con campioni derivati da Umano, Topo, Ratto e S. cerevisiae.
Informazioni su geni e proteine
Riepilogo UniProt
In the cytoplasm, catalyzes the conversion of glucose-6-phosphate to fructose-6-phosphate, the second step in glycolysis, and the reverse reaction during gluconeogenesis (PubMed:28803808). Besides it's role as a glycolytic enzyme, also acts as a secreted cytokine: acts as an angiogenic factor (AMF) that stimulates endothelial cell motility (PubMed:11437381). Acts as a neurotrophic factor, neuroleukin, for spinal and sensory neurons (PubMed:3352745, PubMed:11004567). It is secreted by lectin-stimulated T-cells and induces immunoglobulin secretion (PubMed:3352745, PubMed:11004567).
Sommario di Entrez
This gene encodes a member of the glucose phosphate isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In the cytoplasm, the gene product functions as a glycolytic enzyme (glucose-6-phosphate isomerase) that interconverts glucose-6-phosphate and fructose-6-phosphate. Extracellularly, the encoded protein (also referred to as neuroleukin) functions as a neurotrophic factor that promotes survival of skeletal motor neurons and sensory neurons, and as a lymphokine that induces immunoglobulin secretion. The encoded protein is also referred to as autocrine motility factor based on an additional function as a tumor-secreted cytokine and angiogenic factor. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. Alternative splicing results in multiple transcript variants.
Coinvolgimento nella malattia
Hemolytic anemia, non-spherocytic, due to glucose phosphate isomerase deficiency: A form of anemia in which there is no abnormal hemoglobin or spherocytosis. It is caused by glucose phosphate isomerase deficiency.
Somiglianze di sequenza
Belongs to the GPI family.
Modifica post-translazionale
Phosphorylation at Ser-185 by CK2 has been shown to decrease enzymatic activity and may contribute to secretion by a non-classical secretory pathway.
Posizione cellulare
Cytoplasm. Secreted.
