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Energy metabolism enzyme in Schistosoma species (None established for the entire group; individual enzymes (e.g., enolase, AMPK) have standard abbreviations)

Target
None established for the entire group; individual enzymes (e.g., enolase, AMPK) have standard abbreviations
Molecular classification
Enzyme, Metabolic enzyme, Oxidoreductase (e.g., glycolytic enzymes), Kinase (e.g., AMPK)
01

Overview

Energy metabolism enzymes in Schistosoma species refer to a heterogeneous group of enzymes that catalyze critical steps in glucose uptake, glycolysis, the Krebs cycle, and related metabolic pathways, enabling the parasite’s energetic needs throughout its life cycle. Notable enzymes include enolase, AMP-activated protein kinase (AMPK), and surface phosphatases (such as SmAP), which contribute to both energy extraction from host-derived glucose and metabolic adaptation to varied environments. These enzymes are essential for parasite survival, growth, and pathogenesis, making them attractive targets for anti-schistosomiasis therapies. Many approved and experimental drugs have been identified to interact with specific metabolic enzymes, validating their druggability. However, the lack of selectivity may pose challenges for host safety due to the evolutionary conservation of these enzymes.

Other names
Schistosoma energy metabolism enzymeSchistosome metabolic enzymeSchistosoma glycolytic enzymeMitochondrial enzyme (in Schistosoma)Schistosoma glycolysis enzyme
02

Mechanism of action

Enzymatic inhibition (reduces energy production and parasite survival); Inhibition of glycolysis and Krebs cycle enzymes; Disruption of ATP production; Interference with metabolic adaptation (e.g., AMPK inhibition, glycolytic flux modification)

03

Biological functions

Cellular energy productionGlycolysisGluconeogenesisKrebs cycle (tricarboxylic acid cycle)Oxidative phosphorylationRegulation of glycogen metabolismVitamin metabolism (e.g., vitamin B6 processing)
04

Disease associations

Infection (critical for survival and pathogenesis of Schistosoma spp.)Parasitic disease (Schistosomiasis)
05

Safety considerations

Potential for off-target effects on host metabolic enzymes (risk of host toxicity since enzymes like enolase, AMPK are conserved in humans)Specificity in targeting parasite enzymes required to minimize adverse effectsVariability of enzyme expression across parasite life stages
06

Interacting drugs

Mefloquine (inhibits enolase)

2 more in the full profile.

07

Biomarkers

Alterations in glycolytic, gluconeogenic, pentose phosphate pathway metabolites (e.g., host AMP, ADP, G6P, 3-PG), reflective of parasite energy utilizationEnzyme expression profiles (e.g., enolase, AMPK, SmAP)

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