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Synthesis and activity of piperazine-containing antirhinoviral agents and crystal structure of SDZ 880-061 bound to human rhinovirus 14. |
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The structure of a highly virulent Theiler\'s murine encephalomyelitis virus (GDVII) and implications for determinants of viral persistence. |
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Crystallographers pinpoint what goes where. |
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Neutralizing antibody to human rhinovirus 14 penetrates the receptor-binding canyon. |
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Human rhinovirus 3 at 3.0 A resolution. |
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Zhao R;Pevear DC;Kremer MJ;Giranda VL;Kofron JA;Kuhn RJ;Rossmann MG |
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Cations in human rhinoviruses. |
Virology |
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Structure-based design of peptide presentation on a viral surface: the crystal structure of a plant/animal virus chimera at 2.8 A resolution. |
Fold Des |
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Lin T;Porta C;Lomonossoff G;Johnson JE |
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The refined structure of human rhinovirus 16 at 2.15 A resolution: implications for the viral life cycle. |
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Energetics of quasiequivalence: computational analysis of protein-protein interactions in icosahedral viruses. |
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Modeling RNA-ligand interactions: the Rev-binding element RNA-aminoglycoside complex. |
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A dimeric crystal structure for the N-terminal two domains of intercellular adhesion molecule-1. |
Proc Natl Acad Sci U S A |
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The structure of the two amino-terminal domains of human ICAM-1 suggests how it functions as a rhinovirus receptor and as an LFA-1 integrin ligand. |
Proc Natl Acad Sci U S A |
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Structure of a neutralizing antibody bound monovalently to human rhinovirus 2. |
J Virol |
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Primary and tertiary structures of the Fab fragment of a monoclonal anti-E-selectin 7A9 antibody that inhibits neutrophil attachment to endothelial cells. |
J Biol Chem |
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Antibody-mediated neutralization of human rhinovirus 14 explored by means of cryoelectron microscopy and X-ray crystallography of virus-Fab complexes. |
J Virol |
1998 |
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Tripeptide aldehyde inhibitors of human rhinovirus 3C protease: design, synthesis, biological evaluation, and cocrystal structure solution of P1 glutamine isosteric replacements. |
J Med Chem |
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Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 1. Michael acceptor structure-activity studies. |
J Med Chem |
1998 |
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Structure-based design, synthesis, and biological evaluation of irreversible human rhinovirus 3C protease inhibitors. 2. Peptide structure-activity studies. |
J Med Chem |
1998 |
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