Hepatitis C Virus NS3 Protease Is Activated by Low Concentrations of Protease Inhibitors
Author:
Affiliation:
1. Department of Biochemistry and Organic Chemistry, Uppsala University, BMC, Box 576, SE-751 23 Uppsala, Sweden.
Publisher
American Chemical Society (ACS)
Subject
Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/bi9016928
Reference48 articles.
1. Replication of hepatitis C virus
2. New Developments in the Discovery of Agents to Treat Hepatitis C
3. Multiple Determinants Influence Complex Formation of the Hepatitis C Virus NS3 Protease Domain with Its NS4A Cofactor Peptide
4. Complex Formation between the Hepatitis C Virus Serine Protease and A Synthetic NS4A Cofactor Peptide
5. Crystal Structure of the Hepatitis C Virus NS3 Protease Domain Complexed with a Synthetic NS4A Cofactor Peptide
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1. Characterization of interactions between hepatitis C virus NS5B polymerase, annexin A2 and RNA – effects on NS5B catalysis and allosteric inhibition;Virology Journal;2017-12
2. Identification of Weak Points of Hepatitis C Virus NS3 Protease Inhibitors Using Surface Plasmon Resonance Biosensor-Based Interaction Kinetic Analysis and Genetic Variants;Journal of Medicinal Chemistry;2014-02-26
3. Accounting for strain variations and resistance mutations in the characterization of hepatitis C NS3 protease inhibitors;Journal of Enzyme Inhibition and Medicinal Chemistry;2014-02-11
4. Hepacivirin;Handbook of Proteolytic Enzymes;2013
5. Novel Peptide Mimetics Based on N-protected Amino Acids Derived from Isomannide as Potential Inhibitors of NS3 Serine Protease of Hepatitis C Virus;Letters in Organic Chemistry;2012-04-24
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