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Antimicrobial Agents and Chemotherapy|November 1, 2021
A Combination of Amino Acid Mutations Leads to Resistance to Multiple Nucleoside Analogs in Reverse Transcriptases from HIV-1 Subtypes B and CPaul L Boyer, Catherine A Rehm, Michael C Sneller, et al.Journal of Medicinal Chemistry|July 11, 2003
A conformationally locked analogue of the anti-HIV agent stavudine. An important correlation between pseudorotation and maximum amplitudeYongseok Choi, Clifford George, Maria J Comin, et al.Nucleic Acids Research|August 5, 2008
Crystal engineering of HIV-1 reverse transcriptase for structure-based drug designJoseph D Bauman, Kalyan Das, William C Ho, et al.The EMBO Journal|November 29, 2002
Structures of HIV-1 reverse transcriptase with pre- and post-translocation AZTMP-terminated DNAStefan G Sarafianos, Arthur D Clark, Kalyan Das, et al.Nature Structural & Molecular Biology|September 21, 2010
Structural basis of HIV-1 resistance to AZT by excisionXiongying Tu, Kalyan Das, Qianwei Han, et al.The Journal of Biological Chemistry|January 30, 2003
Trapping HIV-1 reverse transcriptase before and after translocation on DNAStefan G Sarafianos, Arthur D Clark, Steve Tuske, et al.The Journal of Biological Chemistry|October 9, 2009
Structural basis for the role of the K65R mutation in HIV-1 reverse transcriptase polymerization, excision antagonism, and tenofovir resistanceKalyan Das, Rajiv P Bandwar, Kirsten L White, et al.Nature Structural & Molecular Biology|April 27, 2004
Structures of HIV-1 RT-DNA complexes before and after incorporation of the anti-AIDS drug tenofovirSteve Tuske, Stefan G Sarafianos, Arthur D Clark, et al.Bioorganic Chemistry|March 19, 2003
A novel mechanism for inhibition of HIV-1 reverse transcriptaseA Geoffrey Skillman, Karl W Maurer, Diana C Roe, et al.Journal of Computer-Aided Molecular Design|September 19, 2003
On the detection of multiple-binding modes of ligands to proteins, from biological, structural, and modeling dataPaul J Lewi, Marc de Jonge, Frits Daeyaert, et al.Pageof 5