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Viruses|January 25, 2025
Structural Analysis of Inhibitor Binding to Enterovirus-D68 3C ProteaseVincent N Azzolino, Ala M Shaqra, Akbar Ali, et al.Viruses|September 28, 2024
Elucidating the Substrate Envelope of Enterovirus 68-3C Protease: Structural Basis of Specificity and Potential ResistanceVincent N Azzolino, Ala M Shaqra, Akbar Ali, et al.The Journal of Physical Chemistry. B|October 15, 2025
Predicting the Impact of Drug Resistance Mutations on Inhibitor Potency with Molecular Dynamics and Machine LearningLauren E Intravaia, Ala M Shaqra, Somayeh Pirhadi, et al.Viruses|November 27, 2025
Structural Analysis of Inhibitor Binding to the Feline Enteric Coronavirus (FECV) Main ProteaseArooma Maryam, Stephanie A Moquin, Dustin Dovala, et al.ACS Combinatorial Science|January 5, 2019
Post-Glycosylation Diversification (PGD): An Approach for Assembling Collections of Glycosylated Small MoleculesZachary Cannone, Ala M Shaqra, Chris Lorenc, et al.Bioorganic Chemistry|November 29, 2022
Allosteric quinoxaline-based inhibitors of the flavivirus NS2B/NS3 proteaseJacqueto Zephyr, Desaboini Nageswara Rao, Colby Johnson, et al.Viruses|March 30, 2023
Crystal Structures of Inhibitor-Bound Main Protease from Delta- and Gamma-CoronavirusesSarah N Zvornicanin, Ala M Shaqra, Qiuyu J Huang, et al.ACS Infectious Diseases|March 12, 2024
Contributions of Hyperactive Mutations in Mpro from SARS-CoV-2 to Drug ResistanceJulia M Flynn, Sarah N Zvornicanin, Tenzin Tsepal, et al.Mbio|April 4, 2025
Molecular mechanisms of drug resistance and compensation in SARS-CoV-2 main protease: the interplay between E166 and L50Sarah N Zvornicanin, Ala M Shaqra, Julia Flynn, et al.Nucleic Acids Research|March 29, 2025
Next generation APOBEC3 inhibitors: optimally designed for potency and nuclease stabilityAdam K Hedger, Wazo Myint, Jeong Min Lee, et al.Pageof 2