ALDOB - aldolase, fructose-bisphosphate B Gene

Also Known as ALDB; ALDO2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 229

About ALDOB

Cytogenetic location: 9q31.1 Genomic coordinates (GRCh38): 9:101,420,560-101,435,774 (from NCBI)

This gene has 8 transcripts (splice variants), 220 orthologues, 2 paralogues and is associated with 2 phenotypes. Biased expression in kidney (RPKM 2378.7), small intestine (RPKM 1833.7) and 2 other tissues.

Summary

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]

ALDOB Products (1)

mRNA Protein Name
NM_000035.4 NP_000026.2 fructose-bisphosphate aldolase B
Molecular Function GO Annotation Evidence References Source
enables ATPase binding IDA
IDA: Inferred from direct assay
17576770 GOA
enables cytoskeletal protein binding IDA
IDA: Inferred from direct assay
9244396 GOA
enables fructose binding IMP
IMP: Inferred from mutant phenotype
10625657 GOA
enables fructose-1-phosphate aldolase activity IDA
IDA: Inferred from direct assay
2649152 GOA
enables fructose-bisphosphate aldolase activity IDA
IDA: Inferred from direct assay
9244396 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
10625657 GOA
enables molecular adaptor activity IDA
IDA: Inferred from direct assay
35122041 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
18000879 GOA
Biological Process GO Annotation Evidence References Source
involved in NADH oxidation IDA
IDA: Inferred from direct assay
17576770 GOA
involved in fructose 1,6-bisphosphate metabolic process IDA
IDA: Inferred from direct assay
9244396 GOA
involved in fructose metabolic process IMP
IMP: Inferred from mutant phenotype
3383242 GOA
involved in glycolytic process IDA
IDA: Inferred from direct assay
10625657 GOA
involved in negative regulation of pentose-phosphate shunt IMP
IMP: Inferred from mutant phenotype
35122041 GOA
involved in positive regulation of ATP-dependent activity IGI
IGI: Inferred from genetic interaction
17576770 GOA
involved in vacuolar proton-transporting V-type ATPase complex assembly IGI
IGI: Inferred from genetic interaction
17576770 GOA
Cellular Component GO Annotation Evidence References Source
located in centriolar satellite IDA
IDA: Inferred from direct assay
18000879 GOA
located in cytosol IDA
IDA: Inferred from direct assay
35122041 GOA
located in microtubule organizing center IDA
IDA: Inferred from direct assay
18000879 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

ALDOB Protein Structure

Glycolytic

Glycolytic: Fructose-bisphosphate aldolase class-I (15 - 364)

  • 0
  • 100
  • 200
  • 300
  • 364 a.a.
Protein Preferred Names Protein Names

fructose-bisphosphate aldolase B

  • aldolase 2

ALDOB Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ALDOB P05062 BBS1 Homo sapiens Q8NFJ9 18000879
Intra
ALDOB P05062 BBS4 Homo sapiens Q96RK4
Y2H
18000879
Intra
ALDOB P05062 BBS4 Homo sapiens Q96RK4 18000879
Intra
ALDOB P05062 BBS4 Homo sapiens Q96RK4 18000879
Intra
ALDOB P05062 BBS7 Homo sapiens Q8IWZ6 18000879
Intra
ALDOB P05062 BBS7 Homo sapiens Q8IWZ6 18000879
Intra
ALDOB P05062 ALDOA Homo sapiens P04075 33961781
Intra
ALDOB P05062 ALDOA Homo sapiens P04075
Y2H
21988832
Intra
ALDOB P05062 BBS2 Homo sapiens Q9BXC9 18000879
Intra
ALDOB P05062 BBS2 Homo sapiens Q9BXC9 18000879
Intra
ALDOB P05062 BBS2 Homo sapiens Q9BXC9
Y2H
18000879
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant ALDOB Proteins

Cat. No. Product Name Accession Purity
HY-P74419 Aldolase B Protein, Human (GST, solution) P05062 (A2-Y364) ≥ 85%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Fructose Intolerance, Hereditary
  • Hereditary Fructose Intolerance

  • Fructose Intolerance

  • Fructose-1-Phosphate Aldolase Deficiency

  • Fructose-1,6-Bisphosphate Aldolase B Deficiency

  • Aldolase B Deficiency

  • Fructosemia

  • Aldob Deficiency

  • Hereditary Fructose Intolerance Syndrome

  • HFI

  • Fructosaemia

  • Hereditary Fructose-1-Phosphate Aldolase Deficiency

  • Fructose Aldolase B Deficiency

  • Fructose-1,6-Biphosphate Aldolase Deficiency

  • Hereditary Fructosemia

  • Fructosemia, Hereditary

  • Hereditary Fructosaemia

  • Fructose-Biphosphate Aldolase B Deficiency

  • Fructose Intolerance Of Newborn

  • Aldb - [Aldolase B] Deficiency

  • Deficiency Of Fructose-Bisphosphate Aldolase

Fructosuria, Essential
  • Essential Fructosuria

  • Ketohexokinase Deficiency

  • Fructosuria

  • Hepatic Fructokinase Deficiency

  • Fructokinase Deficiency

  • FRUCT

  • Deficiency Of Fructokinase

Hypoglycemia
  • Hypoglycaemia

  • Low Blood Sugar

  • Hypoglycaemia Nos

  • Spontaneous Hypoglycaemia

  • Nondiabetic Hypoglycaemia

  • Hypoglycaemic Disorder Nos

  • Hypoglycaemic Syndrome

Hepatocellular Carcinoma
  • Liver Cancer

  • Primary Liver Cancer

  • HCC

  • Hepatoma

  • Malignant Neoplasm Of Liver

  • Liver Neoplasms

  • Cancer, Hepatocellular

  • Liver Cell Carcinoma

  • Lcc

  • Hepatoblastoma, Somatic

  • Hepatic Cancer

  • Primary Malignant Neoplasm Of Liver

  • Rare Tumor Of Liver And Intrahepatic Biliary Tract

  • Hepatocellular Carcinoma, Somatic

  • Hepatocellular Carcinoma, Childhood Type, Somatic

  • Hepatocellular Cancer, Somatic

  • Ca Liver - Primary

  • Hepatic Neoplasm

  • Malignant Hepato-Biliary Neoplasm

  • Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

  • Malignant Neoplasm Of Liver, Primary

  • Malignant Tumor Of Liver

  • Neoplasm Of Liver

  • Non-Resectable Primary Hepatic Malignant Neoplasm

  • Resectable Malignant Neoplasm Of Liver

  • Resectable Malignant Neoplasm Of The Liver

  • Primary Liver Carcinoma

  • Primary Malignant Liver Neoplasm

  • Primary Cancer Of Liver

  • Primary Tumor Of The Liver

  • Rare Tumor Of Liver And Ibt

  • Hepatocellular Cancer

  • Neoplasm Of The Liver

  • Carcinoma, Hepatocellular

  • Hepatomas

  • Liver Neoplasm

  • Liver Carcinoma

  • Liver And Intrahepatic Biliary Tract Carcinoma

  • Malignant Hepatobiliary Neoplasm

  • Adult Primary Hepatocellular Carcinoma

  • Hepatoblastoma

  • Carcinoma Of Liver

  • Malignant Liver Tumour

  • Malignant Hepatic Tumour

Bardet-Biedl Syndrome
  • Bbs

  • Biedl-Bardet Syndrome

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta ALDOB VGNC VGNC:69791
Felis catus ALDOB VGNC VGNC:59740
Bos taurus ALDOB VGNC VGNC:25822
Canis familiaris ALDOB VGNC VGNC:37792
Rattus norvegicus ALDOB RGD RGD:2090
Mus musculus ALDOB MGD MGI:87995
Others ALDOB NCBI