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Eukaryotic translation elongation factor 1 alpha 2 (eEF1A2) is an isoform of the alpha subunit of the elongation factor-1 complex, which plays a critical role in protein synthesis. It facilitates the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during translational elongation. eEF1A2 is highly expressed in brain, heart, and skeletal muscle. In addition to its role in translation, it binds and bundles actin filaments, influencing cytoskeletal organization. Dysregulation of EEF1A2 is implicated in diseases such as cancer and neurological disorders. Mutations cause severe drug-resistant epilepsy, autism spectrum disorders, and neurodevelopmental delay.
Currently, there are no approved drugs that directly target eEF1A2. Research is ongoing to explore potential therapeutic strategies.
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