Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
Echinoderm microtubule-associated protein-like 3 (EML3) is a microtubule-associated protein localized to spindle microtubules and cytoplasmic microtubules. EML3 regulates mitotic spindle assembly, microtubule–kinetochore attachment, and chromosome alignment during metaphase. It does so by recruiting the Augmin complex and the γ-tubulin ring complex (γ-TuRC) to microtubules, promoting MT-based nucleation required for spindle formation and correct chromosomal segregation. Regulation of EML3 activity is cell cycle-dependent, with cyclin-dependent kinase 1 (CDK1) phosphorylation being critical for its interaction with binding partners. Knockdown of EML3 leads to defects in spindle assembly and chromosome missegregation, implicating it in diseases involving errors in cell division, such as retinitis pigmentosa. Although not currently considered a direct therapeutic target or drug receptor, EML3 has emerging significance in cell biology and disease research.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on Echinoderm microtubule-associated protein-like 3 (EML3).