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Structure paper

TitleDesign, synthesis, and biological evaluation of monopyrrolinone-based HIV-1 protease inhibitors.
Journal, issue, pagesJ. Med. Chem., Vol. 46, Page 1831-1844, Year 2003
Publish dateJan 20, 2003 (structure data deposition date)
AuthorsSmith, A.B. / Cantin, L.D. / Pasternak, A. / Guise-Zawacki, L. / Yao, W. / Charnley, A.K. / Barbosa, J. / Sprengeler, P.A. / Hirschmann, R. / Munshi, S. ...Smith, A.B. / Cantin, L.D. / Pasternak, A. / Guise-Zawacki, L. / Yao, W. / Charnley, A.K. / Barbosa, J. / Sprengeler, P.A. / Hirschmann, R. / Munshi, S. / Olsen, D.B. / Schleif, W.A. / Kuo, L.C.
External linksJ. Med. Chem. / PubMed:12723947
MethodsX-ray diffraction
Resolution2 Å
Structure data

PDB-1npv:
Crystal structure of HIV-1 protease complexed with LDC271
Method: X-RAY DIFFRACTION / Resolution: 2 Å

PDB-1npw:
Crystal structure of HIV protease complexed with LGZ479
Method: X-RAY DIFFRACTION / Resolution: 2 Å

Chemicals

ChemComp-L27:
{1-BENZYL-3-[2-BENZYL-3-OXO-4-(1-OXO-1,2,3,4-TETRAHYDRO- ISOQUINOLIN-4-YL)-2,3-DIHYDRO-1H-PYRROL-2-YL]-2-

ChemComp-HOH:
WATER

ChemComp-LGZ:
CARBAMIC ACID 1-{5-BENZYL-5-[2-HYDROXY-4-PHENYL-3-(TETRAHYDRO-FURAN-

Source
  • human immunodeficiency virus 1
KeywordsHYDROLASE / Protease

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