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TitleDesign, activity, and 2.8 A crystal structure of a C2 symmetric inhibitor complexed to HIV-1 protease.
Journal, issue, pagesScience, Vol. 249, Page 527-533, Year 1990
Publish dateNov 6, 1990 (structure data deposition date)
AuthorsErickson, J. / Neidhart, D.J. / VanDrie, J. / Kempf, D.J. / Wang, X.C. / Norbeck, D.W. / Plattner, J.J. / Rittenhouse, J.W. / Turon, M. / Wideburg, N.
External linksPubMed:2200122
MethodsX-ray diffraction
Resolution2.8 Å
Structure data

PDB-9hvp:
Design, activity and 2.8 Angstroms crystal structure of a C2 symmetric inhibitor complexed to HIV-1 protease
Method: X-RAY DIFFRACTION / Resolution: 2.8 Å

Chemicals

ChemComp-0E9:
benzyl [(1R,4S,6S,9R)-4,6-dibenzyl-5-hydroxy-1,9-bis(1-methylethyl)-2,8,11-trioxo-13-phenyl-12-oxa-3,7,10-triazatridec-1-yl]carbamate

ChemComp-HOH:
WATER

Source
  • human immunodeficiency virus 1
KeywordsHYDROLASE/HYDROLASE INHIBITOR / ACID PROTEINASE / HYDROLASE-HYDROLASE INHIBITOR complex

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