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ALDOB A149P dimer [cytosol]
Stable Identifier
R-HSA-5656445
Type
Complex
Species
Homo sapiens
Compartment
cytosol
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of carbohydrate metabolism (Homo sapiens)
Hereditary fructose intolerance (Homo sapiens)
Defective ALDOB does not cleave Fru 1-P to GA and DHAP (Homo sapiens)
ALDOB mutant proteins [cytosol] (Homo sapiens)
ALDOB A149P dimer [cytosol] (Homo sapiens)
Literature References
PubMed ID
Title
Journal
Year
10625657
Expression, purification, and characterization of natural mutants of human aldolase B. Role of quaternary structure in catalysis
Sygusch, J
,
Cox, TM
,
Rellos, P
J. Biol. Chem.
2000
12464284
The temperature dependence of activity and structure for the most prevalent mutant aldolase B associated with hereditary fructose intolerance
Procious, SL
,
Malay, AD
,
Tolan, DR
Arch. Biochem. Biophys.
2002
Participants
components
x 2
ALDOB A149P [cytosol]
(Homo sapiens)
Participates
as a member of
ALDOB mutant proteins [cytosol] (Homo sapiens)
Disease
Name
Identifier
Synonyms
hereditary fructose intolerance syndrome
DOID:9869
Fructosemia, Fructose-1,6-bisphosphate aldolase B deficiency, Fructosaemia
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