Target intelligence / Profile preview

Fructose-bisphosphate aldolase C (ALDOC)

Target
ALDOC
Molecular classification
Enzyme, Glycolytic enzyme, Class I fructose-bisphosphate aldolase family
01

Overview

Fructose-bisphosphate aldolase C (ALDOC) is a class I glycolytic enzyme predominantly expressed in the brain (notably hippocampus and Purkinje cells), but also found in smooth muscle and neuronal tissues[1][5]. It catalyzes the reversible conversion of fructose-1,6-bisphosphate (and fructose-1-phosphate) into dihydroxyacetone phosphate and glyceraldehyde 3-phosphate—a key step in glycolysis and gluconeogenesis[1][2][4]. Alongside essential roles in energy metabolism and ATP production, ALDOC may also have diverse "moonlighting" functions, including roles in cellular stress response and cytoskeletal regulation[1][7]. Aberrant expression of ALDOC is implicated in various cancers and may serve as a biomarker for certain diseases[4][5]. While specific clinical drugs do not yet target ALDOC, the enzyme is under investigation as an anti-cancer target and as a vaccine antigen for infectious diseases due to its role in pathogen metabolism and immune responses[7].

Other names
Aldolase CALDOCALDCBrain-type aldolaseFructoaldolase CAldolase 3Fructose-1,6-biphosphate triosephosphate lyaseEpididymis secretory sperm binding protein
02

Mechanism of action

Inhibition of glycolytic activity (reducing ATP and anabolic precursors in rapidly proliferating cells, e.g., cancer)[7]. Vaccine antigen (eliciting immune response against pathogens expressing aldolase orthologs)[7].

03

Biological functions

GlycolysisGluconeogenesisATP biosynthesisCellular energy metabolismStress response in hypoxic lung tissueResistance to excitotoxic injury in cerebellar neuronsPotential cytoskeletal regulation and cell motility ("moonlighting" functions)
04

Disease associations

CancerCongenital disorder of glycosylationMuscle disease (biomarker, not causative)Neurodegenerative disease (indirectly implicated via brain expression and energy metabolism)
05

Safety considerations

Systemic inhibition could impair cellular energy metabolism and is likely to affect tissues with high glycolytic activity (brain, muscle), thus off-target toxicity is a concern[7].As ALDOC is highly expressed in the brain, cognitive/neurodevelopmental effects could be safety-limiting.
06

Interacting drugs

No FDA-approved small molecules target ALDOC directly for human disease; several investigational inhibitors are described in anti-cancer and anti-parasitic contexts[7].
07

Biomarkers

Elevated ALDOC/aldolase levels in blood as a biomarker for muscle diseases and muscle injury[4].Upregulation found in several cancers, suggesting exploratory use as diagnostic/prognostic biomarker[4].

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