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Qingjie Xiao

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Open access Aug 2026

Discovery of Novel Druggable Binding Pockets on SARS-CoV-2 PLpro via Fragment Screening and Insights for Structure-Based Inhibitor Design.

A fragment-based drug discovery strategy combined with crystallographic screening and structural similarities among the fragments provide a robust structural framework for the rational design of PLpro inhibitors and support the development of novel antiviral therapeutics.

Tingting Wu, Zheng Zhou, Xingyu Li et al. · 0 citations