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Acta Crystallographica. Section D, Biological Crystallography|February 27, 2001
A distinct binding mode of a hydroxyethylamine isostere inhibitor of HIV-1 proteaseJ Dohnálek, J Hasek, J Dusková, et al.The EMBO Journal|March 1, 1992
An engineered retroviral proteinase from myeloblastosis associated virus acquires pH dependence and substrate specificity of the HIV-1 proteinaseJ Konvalinka, M Horejsí, M Andreánsky, et al.The Prostate|September 30, 2014
Comparative analysis of monoclonal antibodies against prostate-specific membrane antigen (PSMA)J Tykvart, V Navrátil, F Sedlák, et al.Journal of Virology|December 1, 1996
Specific cleavage sites of Nef proteins from human immunodeficiency virus types 1 and 2 for the viral proteasesJ Schorr, R Kellner, O Fackler, et al.FEBS Letters|July 30, 1990
Sub-site preferences of the aspartic proteinase from the human immunodeficiency virus, HIV-1J Konvalinka, P Strop, J Velek, et al.Leukemia|April 1, 1997
Peptide inhibitors of HIV-1 and HIV-2 proteases: a comparative studyI Pichová, J Weber, J Litera, et al.Biochemistry|June 9, 1992
Different requirements for productive interaction between the active site of HIV-1 proteinase and substrates containing -hydrophobic*hydrophobic- or -aromatic*pro- cleavage sitesJ T Griffiths, L H Phylip, J Konvalinka, et al.Archives of Biochemistry and Biophysics|May 1, 1997
Potency comparison of peptidomimetic inhibitors against HIV-1 and HIV-2 proteinases: design of equipotent lead compoundsJ Weber, P Majer, J Litera, et al.The Journal of Biological Chemistry|May 15, 1990
Sensitive, soluble chromogenic substrates for HIV-1 proteinaseA D Richards, L H Phylip, W G Farmerie, et al.European Journal of Biochemistry|January 15, 1998
Configurations of diastereomeric hydroxyethylene isosteres strongly affect biological activities of a series of specific inhibitors of human-immunodeficiency-virus proteinaseJ Konvalinka, J Litera, J Weber, et al.Pageof 3