Target intelligence / Profile preview

Beta-enolase (ENO3)

Target
ENO3
Molecular classification
Enzyme, Glycolytic enzyme, Lyase family (specifically, phosphopyruvate hydratase subfamily)[2][3][4]
01

Overview

Beta-enolase (ENO3) is an enzyme that catalyzes the conversion of 2-phosphoglycerate to phosphoenolpyruvate in glycolysis and is predominantly expressed in adult skeletal and cardiac muscle. It is crucial for energy metabolism, muscle differentiation, development, and regeneration. Mutations in the ENO3 gene cause glycogen storage disease type XIII and are associated with impaired energy production, which can contribute to muscle weakness, exercise intolerance, and cardiac dysfunction. The protein works both as a key metabolic enzyme and as a participant in muscle structure and regulatory protein networks. While ENO3 itself is not a current direct therapeutic target, its role in metabolic and muscle diseases makes it of substantial biomedical interest[2][3][4][1].

Other names
Beta-enolasemuscle-specific enolaseskeletal muscle enolasemuscle enriched enolase2-phospho-D-glycerate hydro-lyaseEnolase 3MSEGSD13enolase 3 (beta, muscle)ENOBENO3muscle enolase[2][3]
02

Mechanism of action

Not directly drug-targeted in clinical use. For related isoenzymes/inhibitors, action would be glycolytic inhibition, leading to reduced ATP production in target muscle cells.

03

Biological functions

Glycolysis (conversion of 2-phosphoglycerate to phosphoenolpyruvate)Muscle developmentMuscle regenerationEnergy production during muscle contractionMyogenesis and metabolic remodeling in muscleInteraction with myofibrillar and sarcomeric proteins (structural role in muscle)[2][3]
04

Disease associations

Glycogen storage disease type XIII (GSD13)Cardiovascular disease (involvement in heart failure and cardiac dysfunction)Muscle myopathies[2][3]
05

Safety considerations

Potential risk of muscle weakness or rhabdomyolysis if β-enolase function is inhibitedGeneral safety concerns for glycolytic enzyme targets include systemic metabolic disturbances[2][3]
06

Interacting drugs

No specific drug interactions are documented in current search results. Enolase enzymes, in general, have been explored as therapeutic targets, but selective muscle (β) enolase inhibitors are not well established in clinical pharmacology.[2][3]
07

Biomarkers

Null (no widely used clinical biomarkers for patient selection or therapeutic monitoring based on ENO3 yet, though reduction in β-enolase activity is seen in metabolic myopathies and muscle disease[3])

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