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A Phenylnorstatine Inhibitor Binding to HIV-1 Protease: Geometry, Protonation and Subsite-Pocket Interactions Analyzed at Atomic Resolution

  1. 1.
    SYSNO ASEP0191691
    Document TypeK - Proceedings Paper (Czech conf.)
    R&D Document TypeConference Paper
    TitleA Phenylnorstatine Inhibitor Binding to HIV-1 Protease: Geometry, Protonation and Subsite-Pocket Interactions Analyzed at Atomic Resolution
    Author(s) Brynda, Jiří (UMG-J) RID
    Řezáčová, Pavlína (UMG-J) RID
    Fábry, Milan (UMG-J) RID
    Hořejší, Magdalena (UMG-J)
    Štouračová, Renata (UMG-J)
    Sedláček, Juraj (UMG-J) RID
    Souček, M. (CZ)
    Hradílek, M. (CZ)
    Lepšík, M. (CZ)
    Konvalinka, J. (CZ)
    Issue data2003
    Source TitleMaterials Structure in Chemistry, Biology, Physics and Technology. - : Czech and Slovak Crystallographic Association - ISSN 1211-5894
    s. 62
    Number of pages1 s.
    ActionMeeting of the Czech and Slovak structural biologists /3./
    Event date11.03.2004-13.03.2004
    VEvent locationNové hrady
    CountryCZ - Czech Republic
    Event typeEUR
    Languageeng - English
    CountryCZ - Czech Republic
    Keywordsinhibitor ; HIV protease ; atomic resolution
    Subject RIVCE - Biochemistry
    R&D ProjectsOE67/1 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    CEZAV0Z5052915 - UMG-J
    AnnotationThe x-ray structure of a complex of HIV-1 protease (PR) with a phenylnorstatine inhibitor Z-Pns-Phe-Glu-Glu-NH2 has been determined at 1.03 A, the highest resolution so far reported for any HIV PR complex. The inhibiot shows subnanomolar Ki values for both the wild-type PR and the variant representing one of the most common mutations linked to resistance developoment. The structure displays a unique pattern of hydrogen bonding to the two catalytic aspartate residues. The high resolution permits to assess the donor/acceptor realtions of this hydrogen bonding and to indicate a proton shared by the two catalytic residues. Structural mechanism for the unimpaired ihnibition of the protease Val82Ala mutant is also suggested, based on energy calculations and analyses.
    WorkplaceInstitute of Molecular Genetics
    ContactNikol Škňouřilová, nikol.sknourilova@img.cas.cz, Tel.: 241 063 217
    Year of Publishing2004

Number of the records: 1  

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