Target intelligence / Profile preview

Fructose-bisphosphate aldolase A (ALDOA)

Target
ALDOA
Molecular classification
Enzyme (specifically a lyase), Glycolytic enzyme, Class I fructose-bisphosphate aldolase
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Overview

Fructose-bisphosphate aldolase A is a key glycolytic enzyme encoded by the *ALDOA* gene on chromosome 16. It catalyzes the reversible cleavage of fructose 1,6-bisphosphate into two three-carbon sugars—glyceraldehyde 3-phosphate and dihydroxyacetone phosphate—in one of the central steps of glycolysis. Three isoforms exist in vertebrates: ALDOA (muscle/erythrocyte), ALDOB (liver/kidney/intestine), and ALDOC (brain). The protein forms a homotetrameric structure with each subunit adopting a TIM-barrel fold typical for class I aldolases. Deficiency leads to myopathy or hemolytic anemia; overexpression has been implicated in several cancers due to its role supporting high rates of aerobic glycolysis ("Warburg effect"). While not yet targeted by approved drugs, it remains an area of interest for anticancer and antiparasitic drug development because its inhibition could selectively impair rapidly proliferating cells reliant on high rates of glucose metabolism.

Other names
Aldolase AALDAFructose 1,6-bisphosphate aldolase AMuscle-type aldolase
02

Mechanism of action

For potential inhibitors—blockade of glycolytic activity by inhibiting the catalytic conversion of fructose 1,6-bisphosphate to triose phosphates; disruption leads to impaired energy production in rapidly dividing cells such as cancer cells or parasites.

03

Biological functions

Glycolysis (catalyzes the reversible cleavage of fructose 1,6-bisphosphate into glyceraldehyde 3-phosphate and dihydroxyacetone phosphate)Gluconeogenesis (reverse reaction)Energy metabolism
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Disease associations

Cancer (overexpression linked to tumor progression/metastasis in some cancers)Myopathy (aldolase A deficiency causes muscle disease)Hemolytic anemia (deficiency can cause this condition)
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Safety considerations

Potential safety concerns with inhibition include disruption of normal glycolysis in healthy tissues—especially muscle and red blood cells—leading to possible myopathy or hemolysis. Targeting must be selective to avoid systemic toxicity due to the enzyme's ubiquitous role in energy metabolism.
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Interacting drugs

No widely approved drugs directly targeting ALDOA are currently used clinically. However, research efforts have explored small-molecule inhibitors for cancer therapy or antiparasitic applications due to its essential metabolic role. No specific drug names are established as direct ALDOA modulators in clinical use.
07

Biomarkers

ALDOA expression levels may serve as biomarkers for certain cancers or metabolic disorders; elevated levels can indicate increased glycolytic activity typical of tumors ("Warburg effect")

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