Preferred Label : glucose-6-phosphate isomerase;

MeSH definition : An aldose-ketose isomerase that catalyzes the reversible interconversion of glucose 6-phosphate and fructose 6-phosphate. In prokaryotic and eukaryotic organisms it plays an essential role in glycolytic and gluconeogenic pathways. In mammalian systems the enzyme is found in the cytoplasm and as a secreted protein. This secreted form of glucose-6-phosphate isomerase has been referred to as autocrine motility factor or neuroleukin, and acts as a cytokine which binds to the AUTOCRINE MOTILITY FACTOR RECEPTOR. Deficiency of the enzyme in humans is an autosomal recessive trait, which results in CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA.;

MeSH synonym : isomerase, glucosephosphate; phosphoglucose isomerase; isomerase, glucose 6 phosphate; isomerase, phosphohexose; phosphohexose isomerase; glucosephosphate isomerase; isomerase, glucose-6-phosphate; isomerase, phosphoglucose; glucose 6 phosphate isomerase;

MeSH hyponym : autocrine motility factor; Motility Factor, Autocrine; Tumor Autocrine Motility Factor; Tumor-Cell Autocrine Motility Factor; Tumor Cell Autocrine Motility Factor; Neuroleukin; Factor, Autocrine Motility;

MeSH CAS label : D-Glucose-6-phosphate ketol-isomerase;

MeSH Related Number : autocrine motility factor; EC 5.3.1.9;

Registry Number MeSH : EC 5.3.1.9;

Related CAS MeSH : EC 5.3.1.9 (Autocrine motility factor);

Wikipedia link : https://en.wikipedia.org/wiki/Glucose-6-phosphate isomerase;

Is substance : O;

UNII : EC 5.3.1.9;

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An aldose-ketose isomerase that catalyzes the reversible interconversion of glucose 6-phosphate and fructose 6-phosphate. In prokaryotic and eukaryotic organisms it plays an essential role in glycolytic and gluconeogenic pathways. In mammalian systems the enzyme is found in the cytoplasm and as a secreted protein. This secreted form of glucose-6-phosphate isomerase has been referred to as autocrine motility factor or neuroleukin, and acts as a cytokine which binds to the AUTOCRINE MOTILITY FACTOR RECEPTOR. Deficiency of the enzyme in humans is an autosomal recessive trait, which results in CONGENITAL NONSPHEROCYTIC HEMOLYTIC ANEMIA.

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glucose-6-phosphate isomerase
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28/04/2025


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