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TitleRole of hydroxyl group and R/S configuration of isostere in binding properties of HIV-1 protease inhibitors
Journal, issue, pagesEur. J. Biochem., Vol. 271, Page 4451-4461, Year 2004
Publish dateJun 12, 2002 (structure data deposition date)
AuthorsPetrokova, H. / Duskova, J. / Dohnalek, J. / Skalova, T. / Vondrackova-Buchtelova, E. / Soucek, M. / Konvalinka, J. / Brynda, J. / Fabry, M. / Sedlacek, J. / Hasek, J.
External linksEur. J. Biochem. / PubMed:15560786
MethodsX-ray diffraction
Resolution2.45 Å
Structure data

PDB-1m0b:
HIV-1 protease in complex with an ethyleneamine inhibitor
Method: X-RAY DIFFRACTION / Resolution: 2.45 Å

Chemicals

ChemComp-0ZQ:
N-{(3S)-3-[(tert-butoxycarbonyl)amino]-4-phenylbutyl}-L-phenylalanyl-L-alpha-glutamyl-L-phenylalaninamide

ChemComp-GOL:
GLYCEROL

ChemComp-HOH:
WATER

Source
  • human immunodeficiency virus 1
KeywordsHYDROLASE/HYDROLASE INHIBITOR / HIV PROTEASE / PEPTIDOMIMETICS / HYDROLASE-HYDROLASE INHIBITOR complex

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