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1SYV

HLA-B*4405 complexed to the dominant self ligand EEFGRAYGF

Summary for 1SYV
Entry DOI10.2210/pdb1syv/pdb
Related1SYS
DescriptorMHC class I antigen, Beta-2-microglobulin, major histocompatibility complex, class II, DR alpha, ... (4 entities in total)
Functional Keywordshla, mhc, class i, b44, immune system
Biological sourceHomo sapiens (human)
More
Cellular locationMembrane; Single-pass type I membrane protein: P30481
Secreted: P61769
Total number of polymer chains3
Total formula weight44997.87
Authors
Primary citationZernich, D.,Purcell, A.W.,Macdonald, W.A.,Kjer-Nielsen, L.,Ely, L.K.,Laham, N.,Crockford, T.,Mifsud, N.A.,Bharadwaj, M.,Chang, L.,Tait, B.D.,Holdsworth, R.,Brooks, A.G.,Bottomley, S.P.,Beddoe, T.,Peh, C.A.,Rossjohn, J.,McCluskey, J.
Natural HLA class I polymorphism controls the pathway of antigen presentation and susceptibility to viral evasion
J.Exp.Med., 200:13-24, 2004
Cited by
PubMed Abstract: HLA class I polymorphism creates diversity in epitope specificity and T cell repertoire. We show that HLA polymorphism also controls the choice of Ag presentation pathway. A single amino acid polymorphism that distinguishes HLA-B*4402 (Asp116) from B*4405 (Tyr116) permits B*4405 to constitutively acquire peptides without any detectable incorporation into the transporter associated with Ag presentation (TAP)-associated peptide loading complex even under conditions of extreme peptide starvation. This mode of peptide capture is less susceptible to viral interference than the conventional loading pathway used by HLA-B*4402 that involves assembly of class I molecules within the peptide loading complex. Thus, B*4402 and B*4405 are at opposite extremes of a natural spectrum in HLA class I dependence on the PLC for Ag presentation. These findings unveil a new layer of MHC polymorphism that affects the generic pathway of Ag loading, revealing an unsuspected evolutionary trade-off in selection for optimal HLA class I loading versus effective pathogen evasion.
PubMed: 15226359
DOI: 10.1084/jem.20031680
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.7 Å)
Structure validation

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