232 related articles for article (PubMed ID: 7527812)
1. Several HLA alleles share overlapping peptide specificities.
Sidney J; del Guercio MF; Southwood S; Engelhard VH; Appella E; Rammensee HG; Falk K; Rötzschke O; Takiguchi M; Kubo RT
J Immunol; 1995 Jan; 154(1):247-59. PubMed ID: 7527812
[TBL] [Abstract][Full Text] [Related]
2. Specificity and degeneracy in peptide binding to HLA-B7-like class I molecules.
Sidney J; Southwood S; del Guercio MF; Grey HM; Chesnut RW; Kubo RT; Sette A
J Immunol; 1996 Oct; 157(8):3480-90. PubMed ID: 8871647
[TBL] [Abstract][Full Text] [Related]
3. Polymorphism in the alpha 1 helix of the HLA-B heavy chain can have an overriding influence on peptide-binding specificity.
Barber LD; Percival L; Arnett KL; Gumperz JE; Chen L; Parham P
J Immunol; 1997 Feb; 158(4):1660-9. PubMed ID: 9029102
[TBL] [Abstract][Full Text] [Related]
4. Self-peptides from four HLA-DR alleles share hydrophobic anchor residues near the NH2-terminal including proline as a stop signal for trimming.
Kropshofer H; Max H; Halder T; Kalbus M; Muller CA; Kalbacher H
J Immunol; 1993 Nov; 151(9):4732-42. PubMed ID: 8409432
[TBL] [Abstract][Full Text] [Related]
5. Binding of a peptide antigen to multiple HLA alleles allows definition of an A2-like supertype.
del Guercio MF; Sidney J; Hermanson G; Perez C; Grey HM; Kubo RT; Sette A
J Immunol; 1995 Jan; 154(2):685-93. PubMed ID: 7529283
[TBL] [Abstract][Full Text] [Related]
6. 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; 46(8-9):1911-7. PubMed ID: 19157553
[TBL] [Abstract][Full Text] [Related]
7. HLA-B15 peptide ligands are preferentially anchored at their C termini.
Prilliman KR; Jackson KW; Lindsey M; Wang J; Crawford D; Hildebrand WH
J Immunol; 1999 Jun; 162(12):7277-84. PubMed ID: 10358176
[TBL] [Abstract][Full Text] [Related]
8. Overlapping peptide-binding specificities of HLA-B27 and B39: evidence for a role of peptide supermotif in the pathogenesis of spondylarthropathies.
Sobao Y; Tsuchiya N; Takiguchi M; Tokunaga K
Arthritis Rheum; 1999 Jan; 42(1):175-81. PubMed ID: 9920028
[TBL] [Abstract][Full Text] [Related]
9. Anti-HLA-E mAb 3D12 mimics MEM-E/02 in binding to HLA-B and HLA-C alleles: Web-tools validate the immunogenic epitopes of HLA-E recognized by the antibodies.
Ravindranath MH; Pham T; El-Awar N; Kaneku H; Terasaki PI
Mol Immunol; 2011 Jan; 48(4):423-30. PubMed ID: 21145594
[TBL] [Abstract][Full Text] [Related]
10. Several common HLA-DR types share largely overlapping peptide binding repertoires.
Southwood S; Sidney J; Kondo A; del Guercio MF; Appella E; Hoffman S; Kubo RT; Chesnut RW; Grey HM; Sette A
J Immunol; 1998 Apr; 160(7):3363-73. PubMed ID: 9531296
[TBL] [Abstract][Full Text] [Related]
11. Definition of specific peptide motifs for four major HLA-A alleles.
Kubo RT; Sette A; Grey HM; Appella E; Sakaguchi K; Zhu NZ; Arnott D; Sherman N; Shabanowitz J; Michel H
J Immunol; 1994 Apr; 152(8):3913-24. PubMed ID: 8144960
[TBL] [Abstract][Full Text] [Related]
12. Naturally occurring A pocket polymorphism in HLA-B*2703 increases the dependence on an accessory anchor residue at P1 for optimal binding of nonamer peptides.
Griffin TA; Yuan J; Friede T; Stevanovic S; Ariyoshi K; Rowland-Jones SL; Rammensee HG; Colbert RA
J Immunol; 1997 Nov; 159(10):4887-97. PubMed ID: 9366414
[TBL] [Abstract][Full Text] [Related]
13. Class I MHC-peptide interaction: structural and functional aspects.
Ruppert J; Kubo RT; Sidney J; Grey HM; Sette A
Behring Inst Mitt; 1994 Jul; (94):48-60. PubMed ID: 7998914
[TBL] [Abstract][Full Text] [Related]
14. Fine tuning of peptide binding to HLA-B*3501 molecules by nonanchor residues.
Schönbach C; Ibe M; Shiga H; Takamiya Y; Miwa K; Nokihara K; Takiguchi M
J Immunol; 1995 Jun; 154(11):5951-8. PubMed ID: 7751638
[TBL] [Abstract][Full Text] [Related]
15. Prominent roles of secondary anchor residues in peptide binding to HLA-A24 human class I molecules.
Kondo A; Sidney J; Southwood S; del Guercio MF; Appella E; Sakamoto H; Celis E; Grey HM; Chesnut RW; Kubo RT; Sette A
J Immunol; 1995 Nov; 155(9):4307-12. PubMed ID: 7594589
[TBL] [Abstract][Full Text] [Related]
16. Sequence and gene transfer analyses of HLA-CwBL18 (HLA-C blank) and HLA-Cw5 genes. Implications for the control of expression and immunogenicity of HLA-C antigens.
Tibensky D; DeMars R; Holowachuk EW; Delovitch TL
J Immunol; 1989 Jul; 143(1):348-55. PubMed ID: 2732471
[TBL] [Abstract][Full Text] [Related]
17. 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; 151(11):5966-74. PubMed ID: 8245441
[TBL] [Abstract][Full Text] [Related]
18. Decamer-like conformation of a nona-peptide bound to HLA-B*3501 due to non-standard positioning of the C terminus.
Menssen R; Orth P; Ziegler A; Saenger W
J Mol Biol; 1999 Jan; 285(2):645-53. PubMed ID: 9878435
[TBL] [Abstract][Full Text] [Related]
19. Role of the polymorphic residues in HLA-DR molecules in allele-specific binding of peptide ligands.
Marshall KW; Liu AF; Canales J; Perahia B; Jorgensen B; Gantzos RD; Aguilar B; Devaux B; Rothbard JB
J Immunol; 1994 May; 152(10):4946-57. PubMed ID: 8176213
[TBL] [Abstract][Full Text] [Related]
20. Definition of an HLA-A3-like supermotif demonstrates the overlapping peptide-binding repertoires of common HLA molecules.
Sidney J; Grey HM; Southwood S; Celis E; Wentworth PA; del Guercio MF; Kubo RT; Chesnut RW; Sette A
Hum Immunol; 1996 Feb; 45(2):79-93. PubMed ID: 8882405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]