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1M6O

Crystal Structure of HLA B*4402 in complex with HLA DPA*0201 peptide

Summary for 1M6O
Entry DOI10.2210/pdb1m6o/pdb
DescriptorHLA class I histocompatibility antigen, BW-44(B-12) B*4402 alpha chain, Beta-2-microglobulin, HLA DPA*0201 peptide, ... (4 entities in total)
Functional Keywordsmhc i, glycoprotein, immune system
Biological sourceHomo sapiens (human)
More
Cellular locationMembrane; Single-pass type I membrane protein: P30481
Secreted: P01884
Total number of polymer chains3
Total formula weight44818.58
Authors
Primary citationMacdonald, W.A.,Purcell, A.W.,Mifsud, N.A.,Ely, L.K.,Williams, D.S.,Chang, L.,Gorman, J.J.,Clements, C.S.,Kjer-Nielsen, L.,Koelle, D.M.,Burrows, S.R.,Tait, B.D.,Holdsworth, R.,Brooks, A.G.,Lovrecz, G.O.,Lu, L.,Rossjohn, J.,McCluskey, J.
A naturally selected dimorphism within the HLA-B44 supertype alters class I structure, peptide repertoire, and T cell recognition.
J.Exp.Med., 198:679-691, 2003
Cited by
PubMed Abstract: HLA-B*4402 and B*4403 are naturally occurring MHC class I alleles that are both found at a high frequency in all human populations, and yet they only differ by one residue on the alpha2 helix (B*4402 Asp156-->B*4403 Leu156). CTLs discriminate between HLA-B*4402 and B*4403, and these allotypes stimulate strong mutual allogeneic responses reflecting their known barrier to hemopoeitic stem cell transplantation. Although HLA-B*4402 and B*4403 share >95% of their peptide repertoire, B*4403 presents more unique peptides than B*4402, consistent with the stronger T cell alloreactivity observed toward B*4403 compared with B*4402. Crystal structures of B*4402 and B*4403 show how the polymorphism at position 156 is completely buried and yet alters both the peptide and the heavy chain conformation, relaxing ligand selection by B*4403 compared with B*4402. Thus, the polymorphism between HLA-B*4402 and B*4403 modifies both peptide repertoire and T cell recognition, and is reflected in the paradoxically powerful alloreactivity that occurs across this "minimal" mismatch. The findings suggest that these closely related class I genes are maintained in diverse human populations through their differential impact on the selection of peptide ligands and the T cell repertoire.
PubMed: 12939341
DOI: 10.1084/jem.20030066
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.6 Å)
Structure validation

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