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  1. 1.   Structure-Based Non-Nucleoside Inhibitor Design: Developing Inhibitors that Are Effective Against Resistant Mutants
  2. Smith,Steven; Pauly,Gary; Hewlett, Katharine; Schneider,Joel; Hughes,Stephen
  3. Chemical biology & drug design. 2020, SEP 17;
  1. 2.   Enhancing polo-like kinase 1 selectivity of polo-box domain-binding peptides
  2. Zhao, Xue Zhi; Hymel, David; Burke, Terrence
  3. BIOORGANIC & MEDICINAL CHEMISTRY. 2017, OCT 1; 25(19 Special Issue: SI): 5041-5049.
  1. 3.   Application of oxime-diversification to optimize ligand interactions within a cryptic pocket of the polo-like kinase 1 polo-box domain
  2. Zhao, X. Z.; Hymel, D.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2016, 15-Oct; 26(20): 5009-5012.
  1. 4.   The "Connection" Between HIV Drug Resistance and RNase H
  2. Delviks-Frankenberry, K. A.; Nikolenko, G. N.; Pathak, V. K.
  3. Viruses-Basel. 2010, Jul; 2(7): 1476-1503.
  1. 5.   A Novel Molecular Mechanism of Dual Resistance to Nucleoside and Nonnucleoside Reverse Transcriptase Inhibitors
  2. Nikolenko, G. N.; Delviks-Frankenberry, K. A.; Pathak, V. K.
  3. Journal of Virology. 2010, May; 84(10): 5238-5249.
  1. 6.   Structural and biochemical studies of retroviral proteases
  2. Wlodawer, A.; Gustchina, A.
  3. Biochimica et Biophysica Acta - Protein Structure & Molecular Enzymology. 2000 1477(1-2): 16-34.
  1. 7.   Drug-Resistant Hiv-1 Proteases Identify Enzyme Residues Important For Substrate Selection and Catalytic Rate
  2. Ridky, T. W.; Kikonyogo, A.; Leis, J.
  3. Biochemistry. 1998 37(39): 13835-13845.
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