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TitlePyrrolidine-5,5-trans-lactams. 4. Incorporation of a P3/P4 urea leads to potent intracellular inhibitors of hepatitis C virus NS3/4A protease
Journal, issue, pagesOrg. Lett., Vol. 5, Page 4627-4630, Year 2003
Publish dateDec 10, 2003 (structure data deposition date)
AuthorsSlater, M.J. / Amphlett, E.M. / Andrews, D.M. / Bamborough, P. / Carey, S.J. / Johnson, M.R. / Jones, P.S. / Mills, G. / Parry, N.R. / Somers, D.O. ...Slater, M.J. / Amphlett, E.M. / Andrews, D.M. / Bamborough, P. / Carey, S.J. / Johnson, M.R. / Jones, P.S. / Mills, G. / Parry, N.R. / Somers, D.O. / Stewart, A.J. / Skarzynski, T.
External linksOrg. Lett. / PubMed:14627400
MethodsX-ray diffraction
Resolution2.75 Å
Structure data

PDB-1rtl:
CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN: NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND PYRROLIDINE-5,5-TRANSLACTAM INHIBITOR
Method: X-RAY DIFFRACTION / Resolution: 2.75 Å

Chemicals

ChemComp-ZN:
Unknown entry

ChemComp-CPX:
N-[(2R,3S)-1-((2S)-2-{[(CYCLOPENTYLAMINO)CARBONYL]AMINO}-3-METHYLBUTANOYL)-2-(1-FORMYL-1-CYCLOBUTYL)PYRROLIDINYL]CYCLOPROPANECARBOXAMIDE

ChemComp-HOH:
WATER

Source
  • hepatitis c virus
KeywordsViral protein complex / VIRAL PROTEIN / SERINE PROTEASE / NONSTRUCTURAL PROTEIN / COFACTOR PEPTIDE / HELICASE / INHIBITOR / TRANSLACTAM

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