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Structure paper

TitlePotent inhibitors of HCV-NS3 protease derived from boronic acids.
Journal, issue, pagesBioorg. Med. Chem. Lett., Vol. 19, Page 180-183, Year 2009
Publish dateOct 20, 2008 (structure data deposition date)
AuthorsVenkatraman, S. / Wu, W. / Prongay, A. / Girijavallabhan, V. / George Njoroge, F.
External linksBioorg. Med. Chem. Lett. / PubMed:19022670
MethodsX-ray diffraction
Resolution2.3 Å
Structure data

PDB-3eyd:
Structure of HCV NS3-4A Protease with an Inhibitor Derived from a Boronic Acid
Method: X-RAY DIFFRACTION / Resolution: 2.3 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-BE8:
[(1R)-2-cyclobutyl-1-({[(1R,2S,5S)-3-(N-{[(1S)-2,2-dimethyl-1-{[methyl(methylsulfonyl)amino]methyl}propyl]carbamoyl}-3-methyl-L-valyl)-6,6-dimethyl-3-azabicyclo[3.1.0]hex-2-yl]carbonyl}amino)ethyl]boronic acid

ChemComp-HOH:
WATER

Source
  • hepatitis c virus subtype 1a
KeywordsVIRAL PROTEIN / Hepatitis C Virus / NS3 Protease Domain / serine protease / boronic acid inhibitor / Envelope protein / Helicase / Hydrolase / Nucleotide-binding / RNA replication / Transmembrane

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