Computational Characterization of Structural Role of the Non-active Site Mutation M36I of Human Immunodeficiency Virus Type 1 Protease
- 10 May 2007
- journal article
- Published by Elsevier in Journal of Molecular Biology
- Vol. 370 (3) , 598-607
- https://doi.org/10.1016/j.jmb.2007.04.081
Abstract
No abstract availableKeywords
This publication has 46 references indexed in Scilit:
- Novel bis -Tetrahydrofuranylurethane-Containing Nonpeptidic Protease Inhibitor (PI) UIC-94017 (TMC114) with Potent Activity against Multi-PI-Resistant Human Immunodeficiency Virus In VitroAntimicrobial Agents and Chemotherapy, 2003
- Tipranavir inhibits broadly protease inhibitor-resistant HIV-1 clinical samplesAIDS, 2000
- BMS-232632, a Highly Potent Human Immunodeficiency Virus Protease Inhibitor That Can Be Used in Combination with Other Available Antiretroviral AgentsAntimicrobial Agents and Chemotherapy, 2000
- Protease sequences from HIV-1 group M subtypes A???H reveal distinct amino acid mutation patterns associated with protease resistance in protease inhibitor-naive individuals worldwideAIDS, 2000
- Weak Binding of VX-478 to Human Plasma Proteins and Implications for Anti-Human Immunodeficiency Virus TherapyThe Journal of Infectious Diseases, 1995
- ABT-538 is a potent inhibitor of human immunodeficiency virus protease and has high oral bioavailability in humans.Proceedings of the National Academy of Sciences, 1995
- L-735,524: an orally bioavailable human immunodeficiency virus type 1 protease inhibitor.Proceedings of the National Academy of Sciences, 1994
- Antiviral properties of Ro 31-8959, an inhibitor of human immunodeficiency virus (HIV) proteinaseAntiviral Research, 1991
- Active human immunodeficiency virus protease is required for viral infectivity.Proceedings of the National Academy of Sciences, 1988
- VIRAL PROTEINASESAnnual Review of Biochemistry, 1988