Target intelligence / Profile preview

Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase (TcGAPDH) (TcGAPDH)

Target
TcGAPDH
Molecular classification
Enzyme, Oxidoreductase, Dehydrogenase
01

Overview

Trypanosoma cruzi glycosomal glyceraldehyde-3-phosphate dehydrogenase (TcGAPDH) is a pivotal enzyme in the glycolytic pathway of the protozoan parasite responsible for Chagas disease (UniProt: P22512). In kinetoplastid parasites like T. cruzi, the initial seven steps of glycolysis are sequestered within specialized peroxisome-like organelles called glycosomes, making this enzyme essential for the parasite's energy metabolism and survival (PubMed: 11061125). Because T. cruzi relies almost exclusively on glycolysis for ATP production during its proliferative and bloodstream stages, inhibiting TcGAPDH effectively starves the parasite of energy. Structural biology studies have revealed significant differences in the NAD+ binding pocket and the catalytic site between the parasite's glycosomal enzyme and the human cytosolic counterpart, which facilitates the design of selective inhibitors (PubMed: 25663131). Various natural and synthetic compounds, including chalcones, flavonoids, and anacardic acids, have demonstrated potent inhibitory activity against TcGAPDH in vitro. Targeting this enzyme remains a highly promising strategy for developing new chemotherapies for American trypanosomiasis, aiming to provide safer and more effective alternatives to current drugs like benznidazole and nifurtimox.

Other names
Glyceraldehyde-3-phosphate dehydrogenase (phosphorylating)gGAPDHGAPDHG3P_TRYCR
02

Mechanism of action

Inhibition of the enzymatic conversion of glyceraldehyde 3-phosphate to 1,3-bisphosphoglycerate by competing with the substrate or the NAD+ cofactor, thereby disrupting the glycolytic pathway and energy production in the parasite.

03

Biological functions

GlycolysisATP productionMetabolic pathwayNAD+ binding
04

Disease associations

InfectionChagas diseaseAmerican trypanosomiasis
05

Safety considerations

Selectivity over human cytosolic glyceraldehyde-3-phosphate dehydrogenase (hGAPDH)Potential off-target inhibition of host glycolytic enzymesMetabolic toxicity in host cells
06

Interacting drugs

Chalcone derivatives

4 more in the full profile.

07

Biomarkers

Parasite loadTcGAPDH enzymatic activity levelsTrypanosoma cruzi DNA (via PCR)

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