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Biochemistry|September 10, 2021
Pan-3C Protease Inhibitor Rupintrivir Binds SARS-CoV-2 Main Protease in a Unique Binding ModeGordon J Lockbaum, Mina Henes, Jeong Min Lee, 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.Journal of Molecular Biology|November 11, 2018
HIV-1 Protease Uses Bi-Specific S2/S2' Subsites to Optimize Cleavage of Two Classes of Target SitesMarc Potempa, Sook-Kyung Lee, Nese Kurt Yilmaz, et al.Journal of Virology|February 1, 2013
Structural and thermodynamic basis of amprenavir/darunavir and atazanavir resistance in HIV-1 protease with mutations at residue 50Seema Mittal, Rajinthna M Bandaranayake, Nancy M King, et al.Journal of the American Chemical Society|August 6, 2014
Drug resistance conferred by mutations outside the active site through alterations in the dynamic and structural ensemble of HIV-1 proteaseDebra A Ragland, Ellen A Nalivaika, Madhavi N L Nalam, et al.ACS Infectious Diseases|December 14, 2018
Structural Adaptation of Darunavir Analogues against Primary Mutations in HIV-1 ProteaseGordon J Lockbaum, Florian Leidner, Linah N Rusere, et al.Viruses|January 28, 2021
Crystal Structure of SARS-CoV-2 Main Protease in Complex with the Non-Covalent Inhibitor ML188Gordon J Lockbaum, Archie C Reyes, Jeong Min Lee, et al.Protein Science : a Publication of the Protein Society|January 16, 2002
Lack of synergy for inhibitors targeting a multi-drug-resistant HIV-1 proteaseNancy M King, Laurence Melnick, Moses Prabu-Jeyabalan, et al.ACS Chemical Biology|June 21, 2012
Extreme entropy-enthalpy compensation in a drug-resistant variant of HIV-1 proteaseNancy M King, Moses Prabu-Jeyabalan, Rajintha M Bandaranayake, et al.Journal of Medicinal Chemistry|August 7, 2019
HIV-1 Protease Inhibitors Incorporating Stereochemically Defined P2' Ligands To Optimize Hydrogen Bonding in the Substrate EnvelopeLinah N Rusere, Gordon J Lockbaum, Sook-Kyung Lee, et al.Pageof 3