Bos taurus Gene: ALDOB
Summary
InnateDB Gene IDBG-637187.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ALDOB
Gene Name fructose-bisphosphate aldolase B
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000015358
Encoded Proteins
fructose-bisphosphate aldolase B
fructose-bisphosphate aldolase B
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000136872:
Fructose-1,6-bisphosphate aldolase (EC 4.1.2.13) is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Vertebrates have 3 aldolase isozymes which are distinguished by their electrophoretic and catalytic properties. Differences indicate that aldolases A, B, and C are distinct proteins, the products of a family of related 'housekeeping' genes exhibiting developmentally regulated expression of the different isozymes. The developing embryo produces aldolase A, which is produced in even greater amounts in adult muscle where it can be as much as 5% of total cellular protein. In adult liver, kidney and intestine, aldolase A expression is repressed and aldolase B is produced. In brain and other nervous tissue, aldolase A and C are expressed about equally. There is a high degree of homology between aldolase A and C. Defects in ALDOB cause hereditary fructose intolerance. [provided by RefSeq, Dec 2008]
Fructose-1,6-bisphosphate aldolase (EC 4.1.2.13) is a tetrameric glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Vertebrates have 3 aldolase isozymes which are distinguished by their electrophoretic and catalytic properties. Differences indicate that aldolases A, B, and C are distinct proteins, the products of a family of related \'housekeeping\' genes exhibiting developmentally regulated expression of the different isozymes. The developing embryo produces aldolase A, which is produced in even greater amounts in adult muscle where it can be as much as 5%% of total cellular protein. In adult liver, kidney and intestine, aldolase A expression is repressed and aldolase B is produced. In brain and other nervous tissue, aldolase A and C are expressed about equally. There is a high degree of homology between aldolase A and C. Defects in ALDOB cause hereditary fructose intolerance. [provided by RefSeq, Dec 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 8:92773692-92865307
Strand Reverse strand
Band
Transcripts
ENSBTAT00000065235 ENSBTAP00000054283
ENSBTAT00000020413 ENSBTAP00000020413
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 12 interaction(s) predicted by orthology.
Predicted by orthology
Total 12 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004332 fructose-bisphosphate aldolase activity
GO:0005515 protein binding
GO:0008092 cytoskeletal protein binding
GO:0016829 lyase activity
GO:0042802 identical protein binding
GO:0051117 ATPase binding
GO:0070061 fructose binding
Biological Process
GO:0006000 fructose metabolic process
GO:0006096 glycolytic process
GO:0006116 NADH oxidation
GO:0030388 fructose 1,6-bisphosphate metabolic process
GO:0032781 positive regulation of ATPase activity
GO:0070072 vacuolar proton-transporting V-type ATPase complex assembly
Cellular Component
GO:0005815 microtubule organizing center
GO:0034451 centriolar satellite
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Fructose catabolism pathway
Glycolysis pathway
Gluconeogenesis pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Metabolism pathway
Disease pathway
Glucose metabolism pathway
Glycogen storage diseases pathway
Disease pathway
Glycolysis pathway
Glucose metabolism pathway
Metabolism pathway
Fructose catabolism pathway
Gluconeogenesis pathway
Glycogen storage diseases pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
KEGG
Glycolysis / Gluconeogenesis pathway
Pentose phosphate pathway pathway
Fructose and mannose metabolism pathway
Pentose phosphate pathway pathway
Fructose and mannose metabolism pathway
Glycolysis / Gluconeogenesis pathway
INOH
Glycolysis Gluconeogenesis pathway
Fructose Mannose metabolism pathway
Pentose phosphate cycle pathway
PID NCI
FOXA2 and FOXA3 transcription factor networks
Cross-References
SwissProt
TrEMBL A5PK73
UniProt Splice Variant
Entrez Gene 515263
UniGene Bt.46035
RefSeq NM_001034485
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC142385 DAAA02024308 DAAA02024309 DAAA02024310 DAAA02024311
GenPept AAI42386
RNA Seq Atlas 515263