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Journal Abstract Search

268 related items for PubMed ID: 9719645

  • 21. Qa-2 molecules are peptide receptors of higher stringency than ordinary class I molecules.
    Rötzschke O, Falk K, Stevanović S, Grahovac B, Soloski MJ, Jung G, Rammensee HG.
    Nature; 1993 Feb 18; 361(6413):642-4. PubMed ID: 8437623
    [Abstract] [Full Text] [Related]

  • 22. Class I MHC-peptide interactions: structural requirements and functional implications.
    Grey HM, Ruppert J, Vitiello A, Sidney J, Kast WM, Kubo RT, Sette A.
    Cancer Surv; 1995 Feb 18; 22():37-49. PubMed ID: 7536628
    [Abstract] [Full Text] [Related]

  • 23. Design of enhanced agonists through the use of a new virtual screening method: application to peptides that bind class I major histocompatibility complex (MHC) molecules.
    Madurga S, Belda I, Llorà X, Giralt E.
    Protein Sci; 2005 Aug 18; 14(8):2069-79. PubMed ID: 16046628
    [Abstract] [Full Text] [Related]

  • 24. MHC/peptide binding studies indicate hierarchy of anchor residues.
    Deres K, Beck W, Faath S, Jung G, Rammensee HG.
    Cell Immunol; 1993 Oct 01; 151(1):158-67. PubMed ID: 8402926
    [Abstract] [Full Text] [Related]

  • 25. Predicting peptide binding to MHC pockets via molecular modeling, implicit solvation, and global optimization.
    Schafroth HD, Floudas CA.
    Proteins; 2004 Feb 15; 54(3):534-56. PubMed ID: 14748001
    [Abstract] [Full Text] [Related]

  • 26. A molecular basis for how a single TCR interfaces multiple ligands.
    Boesteanu A, Brehm M, Mylin LM, Christianson GJ, Tevethia SS, Roopenian DC, Joyce S.
    J Immunol; 1998 Nov 01; 161(9):4719-27. PubMed ID: 9794402
    [Abstract] [Full Text] [Related]

  • 27. Alternative peptide binding motifs of Qa-2 class Ib molecules define rules for binding of self and nonself peptides.
    Tabaczewski P, Chiang E, Henson M, Stroynowski I.
    J Immunol; 1997 Sep 15; 159(6):2771-81. PubMed ID: 9300698
    [Abstract] [Full Text] [Related]

  • 28. Comparative modeling of marsupial MHC class I molecules identifies structural polymorphisms affecting functional motifs.
    Daly K, Church WB, Nicholas K, Williamson P.
    J Exp Zool A Ecol Genet Physiol; 2007 Nov 01; 307(11):611-24. PubMed ID: 17853390
    [Abstract] [Full Text] [Related]

  • 29. Immune recognition of viral antigens.
    Wilson IA, Stanfield RL, Jewell DA, Ghiara JB, Fremont DH, Stura EA.
    Infect Agents Dis; 1994 Nov 01; 3(2-3):155-62. PubMed ID: 7812653
    [Abstract] [Full Text] [Related]

  • 30. Analysis of the structure of naturally processed peptides bound by class I and class II major histocompatibility complex molecules.
    Appella E, Padlan EA, Hunt DF.
    EXS; 1995 Nov 01; 73():105-19. PubMed ID: 7579970
    [Abstract] [Full Text] [Related]

  • 31. Structural implications for the design of molecular vaccines.
    Apostolopoulos V, Yu M, McKenzie IF, Wilson IA.
    Curr Opin Mol Ther; 2000 Feb 01; 2(1):29-36. PubMed ID: 11249650
    [Abstract] [Full Text] [Related]

  • 32. Energetics and cooperativity of the hydrogen bonding and anchor interactions that bind peptides to MHC class II protein.
    McFarland BJ, Katz JF, Sant AJ, Beeson C.
    J Mol Biol; 2005 Jul 01; 350(1):170-83. PubMed ID: 15921691
    [Abstract] [Full Text] [Related]

  • 33. Structure-based prediction of MHC-peptide association: algorithm comparison and application to cancer vaccine design.
    Schiewe AJ, Haworth IS.
    J Mol Graph Model; 2007 Oct 01; 26(3):667-75. PubMed ID: 17493854
    [Abstract] [Full Text] [Related]

  • 34. Naturally processed HLA class I bound peptides from c-myc-transfected cells reveal allele-specific motifs.
    Harris PE, Colovai A, Liu Z, Dalla Favera R, Suciu-Foca N.
    J Immunol; 1993 Dec 01; 151(11):5966-74. PubMed ID: 8245441
    [Abstract] [Full Text] [Related]

  • 35. Peptide-binding motifs for the I-Ad MHC class II molecule: alternate pH-dependent binding behavior.
    Chaves FA, Richards KA, Torelli A, Wedekind J, Sant AJ.
    Biochemistry; 2006 May 23; 45(20):6426-33. PubMed ID: 16700553
    [Abstract] [Full Text] [Related]

  • 36. The relative energetic contributions of dominant P1 pocket versus hydrogen bonding interactions to peptide:class II stability: implications for the mechanism of DM function.
    Bandyopadhyay A, Arneson L, Beeson C, Sant AJ.
    Mol Immunol; 2008 Mar 23; 45(5):1248-57. PubMed ID: 17980431
    [Abstract] [Full Text] [Related]

  • 37. Interactions between immunogenic peptides and MHC proteins.
    Rothbard JB, Gefter ML.
    Annu Rev Immunol; 1991 Mar 23; 9():527-65. PubMed ID: 1910688
    [Abstract] [Full Text] [Related]

  • 38. The peptide length specificity of some HLA class I alleles is very broad and includes peptides of up to 25 amino acids in length.
    Bell MJ, Burrows JM, Brennan R, Miles JJ, Tellam J, McCluskey J, Rossjohn J, Khanna R, Burrows SR.
    Mol Immunol; 2009 May 23; 46(8-9):1911-7. PubMed ID: 19157553
    [Abstract] [Full Text] [Related]

  • 39. Emerging principles for the recognition of peptide antigens by MHC class I molecules.
    Matsumura M, Fremont DH, Peterson PA, Wilson IA.
    Science; 1992 Aug 14; 257(5072):927-34. PubMed ID: 1323878
    [Abstract] [Full Text] [Related]

  • 40. Peptide analysis, stability studies, and structural modeling explain contradictory peptide motifs and unique properties of the NOD mouse MHC class II molecule H2-A(g7).
    Münz C, Hofmann M, Yoshida K, Moustakas AK, Kikutani H, Stevanoviç S, Papadopoulos GK, Rammensee HG.
    Eur J Immunol; 2002 Aug 14; 32(8):2105-16. PubMed ID: 12209622
    [Abstract] [Full Text] [Related]

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