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Journal Abstract Search


293 related items for PubMed ID: 9731777

  • 1. Conserved mode of peptidomimetic inhibition and substrate recognition of human cytomegalovirus protease.
    Tong L, Qian C, Massariol MJ, Déziel R, Yoakim C, Lagacé L.
    Nat Struct Biol; 1998 Sep; 5(9):819-26. PubMed ID: 9731777
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  • 2. Human cytomegalovirus protease complexes its substrate recognition sequences in an extended peptide conformation.
    LaPlante SR, Aubry N, Bonneau PR, Cameron DR, Lagacé L, Massariol MJ, Montpetit H, Plouffe C, Kawai SH, Fulton BD, Chen Z, Ni F.
    Biochemistry; 1998 Jul 07; 37(27):9793-801. PubMed ID: 9657693
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  • 3. Three-dimensional structure of human cytomegalovirus protease.
    Shieh HS, Kurumbail RG, Stevens AM, Stegeman RA, Sturman EJ, Pak JY, Wittwer AJ, Palmier MO, Wiegand RC, Holwerda BC, Stallings WC.
    Nature; 1996 Sep 19; 383(6597):279-82. PubMed ID: 8805708
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  • 4. Structural and biochemical studies of inhibitor binding to human cytomegalovirus protease.
    Khayat R, Batra R, Qian C, Halmos T, Bailey M, Tong L.
    Biochemistry; 2003 Feb 04; 42(4):885-91. PubMed ID: 12549906
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  • 5. Molecular mechanism for dimerization to regulate the catalytic activity of human cytomegalovirus protease.
    Batra R, Khayat R, Tong L.
    Nat Struct Biol; 2001 Sep 04; 8(9):810-7. PubMed ID: 11524687
    [Abstract] [Full Text] [Related]

  • 6. Structure-function relationship of serine protease-protein inhibitor interaction.
    Otlewski J, Jaskólski M, Buczek O, Cierpicki T, Czapińska H, Krowarsch D, Smalas AO, Stachowiak D, Szpineta A, Dadlez M.
    Acta Biochim Pol; 2001 Sep 04; 48(2):419-28. PubMed ID: 11732612
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  • 7. A new serine-protease fold revealed by the crystal structure of human cytomegalovirus protease.
    Tong L, Qian C, Massariol MJ, Bonneau PR, Cordingley MG, Lagacé L.
    Nature; 1996 Sep 19; 383(6597):272-5. PubMed ID: 8805706
    [Abstract] [Full Text] [Related]

  • 8. The 2.2 A crystal structure of human chymase in complex with succinyl-Ala-Ala-Pro-Phe-chloromethylketone: structural explanation for its dipeptidyl carboxypeptidase specificity.
    Pereira PJ, Wang ZM, Rubin H, Huber R, Bode W, Schechter NM, Strobl S.
    J Mol Biol; 1999 Feb 12; 286(1):163-73. PubMed ID: 9931257
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  • 16. Variability of the canonical loop conformations in serine proteinases inhibitors and other proteins.
    Apostoluk W, Otlewski J.
    Proteins; 1998 Sep 01; 32(4):459-74. PubMed ID: 9726416
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  • 17. Active site cavity of herpesvirus proteases revealed by the crystal structure of herpes simplex virus protease/inhibitor complex.
    Hoog SS, Smith WW, Qiu X, Janson CA, Hellmig B, McQueney MS, O'Donnell K, O'Shannessy D, DiLella AG, Debouck C, Abdel-Meguid SS.
    Biochemistry; 1997 Nov 18; 36(46):14023-9. PubMed ID: 9369473
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  • 18. Thermodynamic criterion for the conformation of P1 residues of substrates and of inhibitors in complexes with serine proteinases.
    Qasim MA, Lu SM, Ding J, Bateman KS, James MN, Anderson S, Song J, Markley JL, Ganz PJ, Saunders CW, Laskowski M.
    Biochemistry; 1999 Jun 01; 38(22):7142-50. PubMed ID: 10353824
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  • 19. Crystal structure of cancer chemopreventive Bowman-Birk inhibitor in ternary complex with bovine trypsin at 2.3 A resolution. Structural basis of Janus-faced serine protease inhibitor specificity.
    Koepke J, Ermler U, Warkentin E, Wenzl G, Flecker P.
    J Mol Biol; 2000 May 05; 298(3):477-91. PubMed ID: 10772864
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  • 20. A novel substrate-binding pocket interaction restricts the specificity of the human NK cell-specific serine protease, Met-ase-1.
    Smyth MJ, O'Connor MD, Trapani JA, Kershaw MH, Brinkworth RI.
    J Immunol; 1996 Jun 01; 156(11):4174-81. PubMed ID: 8666785
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