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Aldolase B information


ALDOB
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesALDOB, Aldob, Aldo-2, Aldo2, BC016435, ALDB, aldolase, fructose-bisphosphate B
External IDsOMIM: 612724; MGI: 87995; HomoloGene: 20060; GeneCards: ALDOB; OMA:ALDOB - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000035

NM_144903

RefSeq (protein)

NP_000026

NP_659152

Location (UCSC)Chr 9: 101.42 – 101.45 MbChr 4: 49.54 – 49.55 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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.[5]

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.[6][7][8] Defects in this gene have been identified as the cause of hereditary fructose intolerance (HFI).[9]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000136872 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000028307 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Dalby AR, Tolan DR, Littlechild JA (November 2001). "The structure of human liver fructose-1,6-bisphosphate aldolase". Acta Crystallogr. D. 57 (Pt 11): 1526–33. doi:10.1107/S0907444901012719. PMID 11679716.
  6. ^ "Entrez Gene: ALDOB aldolase B, fructose-bisphosphate".
  7. ^ Henry I, Gallano P, Besmond C, Weil D, Mattei MG, Turleau C, Boué J, Kahn A, Junien C (July 1985). "The structural gene for aldolase B (ALDB) maps to 9q13----32". Ann. Hum. Genet. 49 (Pt 3): 173–80. doi:10.1111/j.1469-1809.1985.tb01691.x. PMID 3000275. S2CID 10058239.
  8. ^ Tolan DR, Penhoet EE (June 1986). "Characterization of the human aldolase B gene". Mol. Biol. Med. 3 (3): 245–64. PMID 3016456.
  9. ^ Cox TM (January 1994). "Aldolase B and fructose intolerance". FASEB J. 8 (1): 62–71. doi:10.1096/fasebj.8.1.8299892. PMID 8299892. S2CID 39102274.

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Aldolase B

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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...

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Hereditary fructose intolerance

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inborn error of fructose metabolism caused by a deficiency of the enzyme aldolase B. Individuals affected with HFI are asymptomatic until they ingest fructose...

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Aldolase A

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Aldolase A (ALDOA, or ALDA), also known as fructose-bisphosphate aldolase, is an enzyme that in humans is encoded by the ALDOA gene on chromosome 16....

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List of aldolases

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Unqualified, aldolase usually refers to the enzyme fructose-bisphosphate aldolase. Aldolase may also refer to: Aldolase A Aldolase B Aldolase C 17a-hydroxyprogesterone...

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Fructose

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fructokinase initially produces fructose 1-phosphate, which is split by aldolase B to produce the trioses dihydroxyacetone phosphate (DHAP) and glyceraldehyde...

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Fructolysis

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Fructose-1-phosphate then undergoes hydrolysis by fructose-1-phosphate aldolase (aldolase B) to form dihydroxyacetone phosphate (DHAP) and glyceraldehyde; DHAP...

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Aldolase C

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Aldolase C, fructose-bisphosphate (ALDOC, or ALDC), is an enzyme that, in humans, is encoded by the ALDOC gene on chromosome 17. This gene encodes a member...

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Inborn errors of carbohydrate metabolism

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and death. HFI is caused by a deficiency of fructose 1,6-biphosphate aldolase in the liver, kidney cortex and small intestine. Infants and adults are...

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Aldolase A deficiency

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Aldolase A deficiency is an autosomal recessive metabolic disorder resulting in a deficiency of the enzyme aldolase A; the enzyme is found predominantly...

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Essential fructosuria

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of fructose in the blood (fructosemia), is caused by a deficiency of aldolase B, the second enzyme involved in the metabolism of fructose. [citation needed]...

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BECN1

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et al. (February 2004). "Genes encoding Pir51, Beclin 1, RbAp48 and aldolase b are up or down-regulated in human primary hepatocellular carcinoma". World...

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They are Nε-trimethyllysine hydroxylase, 3-hydroxy-Nε-trimethyllysine aldolase, 4-N-trimethylaminobutyraldehyde dehydrogenase and γ-butyrobetaine hydroxylase...

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Dihydroneopterin aldolase

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The enzyme dihydroneopterin aldolase (EC 4.1.2.25) catalyzes the chemical reaction 2-amino-4-hydroxy-6-(D-erythro-1,2,3-trihydroxypropyl)-7,8- dihydropteridine...

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Benzoin aldolase

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The enzyme benzoin aldolase (EC 4.1.2.38) catalyzes the chemical reaction 2-hydroxy-1,2-diphenylethanone ⇌ {\displaystyle \rightleftharpoons } 2 benzaldehyde...

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Calvin cycle

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dihydroxyacetone phosphate (DHAP), also a 3-carbon molecule.[citation needed] Aldolase and fructose-1,6-bisphosphatase convert a G3P and a DHAP into fructose...

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Acetaldehyde dehydrogenase

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bifunctional heterodimer with metal-dependent 4-hydroxy-2-ketovalerate aldolase. Utilized in the bacterial degradation of toxic aromatic compounds, the...

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Gluconeogenesis

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contain a bifunctional fructose 1,6-bisphosphate (FBP) aldolase/phosphatase with both FBP aldolase and FBP phosphatase activity. This enzyme is missing...

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Thermus aquaticus

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1970, Freeze and Brock published an article describing a thermostable aldolase enzyme from T. aquaticus. The first polymerase enzyme isolated from T....

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Enzyme catalysis

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formation using the free amine from a lysine residue, as seen in the enzyme aldolase during glycolysis. Some enzymes utilize non-amino acid cofactors such as...

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Malaria antigen detection tests

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doi:10.1021/bi049892w. PMID 15147206. Meier B, Döbeli H, Certa U (1992). "Stage-specific expression of aldolase isoenzymes in the rodent malaria parasite...

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Transaldolase

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intermediate complex of transaldolase B from Escherichia coli: mechanistic implications for class I aldolases". Protein Sci. 6 (1): 119–24. doi:10.1002/pro...

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(addition) stage of the process—the aldol reaction itself—as catalyzed by aldolases. However, the first step is formally an addition reaction rather than...

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