Structure-based discovery of hydrocarbon-stapled paxillin peptides that block FAK scaffolding in cancer
Abstract The focal adhesion kinase (FAK) scaffold provides FAK-targeted cancer therapeutics with greater efficacy and specificity than traditional kinase inhibitors. The FAK scaffold function largely involves the interaction between FAK’s focal adhesion targeting (FAT) domain and paxillin, ultimatel...
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| Huvudupphov: | , , , , , , , , , , , , , , , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Utgiven: |
Nature Portfolio
2025-02-01
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| Serie: | Nature Communications |
| Länkar: | https://doi.org/10.1038/s41467-025-57196-9 |
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