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Bauman JD

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Title Authors Year Journal
Detecting allosteric sites of HIV-1 reverse transcriptase by X-ray crystallographic fragment screening. Bauman JD 2013 Journal of medicinal chemistry
Extension into the entrance channel of HIV-1 reverse transcriptase-Crystallography and enhanced solubility. Bauman JD 2013 Bioorganic & medicinal chemistry letters
Snapshot of the equilibrium dynamics of a drug bound to HIV-1 reverse transcriptase. Bauman JD 2013 Nature chemistry
HIV-1 reverse transcriptase complex with DNA and nevirapine reveals non-nucleoside inhibition mechanism. Bauman JD 2012 Nature structural & molecular biology
A comparison of the ability of rilpivirine (TMC278) and selected analogues to inhibit clinically relevant HIV-1 reverse transcriptase mutants. Bauman JD 2012 Retrovirology
Crystal structure of tert-butyldimethylsilyl-spiroaminooxathioledioxide-thymine (TSAO-T) in complex with HIV-1 reverse transcriptase (RT) redefines the elastic limits of the non-nucleoside inhibitor-binding pocket. Bauman JD 2011 Journal of medicinal chemistry
Identification of alternative binding sites for inhibitors of HIV-1 ribonuclease H through comparative analysis of virtual enrichment studies. Bauman JD 2011 Journal of chemical information and modeling
Fragment Screening and HIV Therapeutics. Bauman JD 2011 Topics in current chemistry
Synthesis, activity, and structural analysis of novel α-hydroxytropolone inhibitors of human immunodeficiency virus reverse transcriptase-associated ribonuclease H. Bauman JD 2011 Journal of medicinal chemistry
Structural basis of HIV-1 resistance to AZT by excision. Bauman JD 2010 Nature structural & molecular biology
Crystallographic study of a novel subnanomolar inhibitor provides insight on the binding interactions of alkenyldiarylmethanes with human immunodeficiency virus-1 reverse transcriptase. Bauman JD 2009 J Med Chem
Structure of HIV-1 reverse transcriptase with the inhibitor beta-Thujaplicinol bound at the RNase H active site. Bauman JD 2009 Structure (London, England : 1993)
High-resolution structures of HIV-1 reverse transcriptase/TMC278 complexes: strategic flexibility explains potency against resistance mutations. Bauman JD 2008 Proceedings of the National Academy of Sciences of the United States of America
Two-dimensional infrared spectra reveal relaxation of the nonnucleoside inhibitor TMC278 complexed with HIV-1 reverse transcriptase. Bauman JD 2008 Proceedings of the National Academy of Sciences of the United States of America
Crystal engineering of HIV-1 reverse transcriptase for structure-based drug design. Bauman JD 2008 Nucleic acids research

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