Structure-based discovery of dengue virus protease inhibitors
- 21 February 2009
- journal article
- review article
- Published by Elsevier in Antiviral Research
- Vol. 82 (3) , 110-114
- https://doi.org/10.1016/j.antiviral.2009.02.190
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Molecular targets for flavivirus drug discoveryPublished by Elsevier ,2008
- Accurate Reproduction of 161 Small-Molecule Complex Crystal Structures using the EUDOC Program: Expanding the Use of EUDOC to Supramolecular ChemistryPLOS ONE, 2007
- Structural basis for the activation of flaviviral NS3 proteases from dengue and West Nile virusNature Structural & Molecular Biology, 2006
- Peptide inhibitors of dengue virus NS3 protease. Part 1: WarheadPublished by Elsevier ,2005
- Peptide inhibitors of dengue virus NS3 protease. Part 2: SAR study of tetrapeptide aldehyde inhibitorsBioorganic & Medicinal Chemistry Letters, 2005
- Competitive inhibition of the dengue virus NS3 serine protease by synthetic peptides representing polyprotein cleavage sitesBiochemical and Biophysical Research Communications, 2005
- EUDOC: a computer program for identification of drug interaction sites in macromolecules and drug leads from chemical databasesJournal of Computational Chemistry, 2001
- RETRACTED: Crystal structure of dengue virus NS3 protease in complex with a bowman-birk inhibitor: implications for flaviviral polyprotein processing and drug designJournal of Molecular Biology, 2000
- Perspectives for the Treatment of Infections with FlaviviridaeClinical Microbiology Reviews, 2000
- SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modelingElectrophoresis, 1997