| ALDOB |
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| Identifiers |
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| Aliases | ALDOB, Aldob, Aldo-2, Aldo2, BC016435, ALDB, aldolase, fructose-bisphosphate B |
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| External IDs | OMIM: 612724; MGI: 87995; HomoloGene: 20060; GeneCards: ALDOB; OMA:ALDOB - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 4 (mouse) |
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| | Band | 4 B1|4 26.57 cM | Start | 49,535,995 bp |
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| End | 49,549,546 bp |
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| Wikidata |
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Aldolase B also known as fructose-bisphosphate aldolase B or liver-type aldolase is one of three isoenzymes (A, B, and C) of the class I fructose 1,6-bisphosphate aldolase enzyme (EC 4.1.2.13), and plays a key role in both glycolysis and gluconeogenesis. The generic fructose 1,6-bisphosphate aldolase enzyme catalyzes the reversible cleavage of fructose 1,6-bisphosphate (FBP) into glyceraldehyde 3-phosphate and dihydroxyacetone phosphate (DHAP) as well as the reversible cleavage of fructose 1-phosphate (F1P) into glyceraldehyde and dihydroxyacetone phosphate. In mammals, aldolase B is preferentially expressed in the liver, while aldolase A is expressed in muscle and erythrocytes and aldolase C is expressed in the brain. Slight differences in isozyme structure result in different activities for the two substrate molecules: FBP and fructose 1-phosphate. Aldolase B exhibits no preference and thus catalyzes both reactions, while aldolases A and C prefer FBP.
In humans, aldolase B is encoded by the ALDOB gene located on chromosome 9. The gene is 14,500 base pairs long and contains 9 exons. Defects in this gene have been identified as the cause of hereditary fructose intolerance (HFI).