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Proteolysis-targeting chimeras (PROTACs) selectively eliminate detrimental proteins by exploiting the ubiquitin-proteasome system (UPS), representing a promising therapeutic strategy against various diseases. Effective adaptations of degradation signal sequences and E3 ligases for PROTACs remain limited. Here, we employed three amino acids─Gly, Pro, and Lys─as the ligand to recruit the corresponding E3 ligases: CRL2
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Jianchao Zhang
Southern University of Science and Technology
Xiao Chen
Southern University of Science and Technology
Congli Chen
Journal of Medicinal Chemistry
Chinese Academy of Sciences
Southern University of Science and Technology
Shenzhen Institutes of Advanced Technology
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Zhang et al. (Thu,) studied this question.
synapsesocial.com/papers/68e5cfeeb6db643587565ee0 — DOI: https://doi.org/10.1021/acs.jmedchem.4c00208
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