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5T70

KIR3DL1 in complex with HLA-B*57:01 presenting TSNLQEQIGW

Summary for 5T70
Entry DOI10.2210/pdb5t70/pdb
Related5T6W 5T6X 5T6Y 5T6Z
DescriptorHLA class I histocompatibility antigen, B-57 alpha chain, Beta-2-microglobulin, Killer cell immunoglobulin-like receptor 3DL1, ... (6 entities in total)
Functional Keywordshuman leukocyte antigen immunoglobulin domain antigen presentation, immune system
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains4
Total formula weight78399.67
Authors
Pymm, P.,Rossjohn, J.,Vivian, J.P. (deposition date: 2016-09-02, release date: 2017-03-01, Last modification date: 2024-11-20)
Primary citationPymm, P.,Illing, P.T.,Ramarathinam, S.H.,O'Connor, G.M.,Hughes, V.A.,Hitchen, C.,Price, D.A.,Ho, B.K.,McVicar, D.W.,Brooks, A.G.,Purcell, A.W.,Rossjohn, J.,Vivian, J.P.
MHC-I peptides get out of the groove and enable a novel mechanism of HIV-1 escape.
Nat. Struct. Mol. Biol., 24:387-394, 2017
Cited by
PubMed Abstract: Major histocompatibility complex class I (MHC-I) molecules play a crucial role in immunity by capturing peptides for presentation to T cells and natural killer (NK) cells. The peptide termini are tethered within the MHC-I antigen-binding groove, but it is unknown whether other presentation modes occur. Here we show that 20% of the HLA-B*57:01 peptide repertoire comprises N-terminally extended sets characterized by a common motif at position 1 (P1) to P2. Structures of HLA-B*57:01 presenting N-terminally extended peptides, including the immunodominant HIV-1 Gag epitope TW10 (TSTLQEQIGW), showed that the N terminus protrudes from the peptide-binding groove. The common escape mutant TSNLQEQIGW bound HLA-B*57:01 canonically, adopting a dramatically different conformation than the TW10 peptide. This affected recognition by killer cell immunoglobulin-like receptor (KIR) 3DL1 expressed on NK cells. We thus define a previously uncharacterized feature of the human leukocyte antigen class I (HLA-I) immunopeptidome that has implications for viral immune escape. We further suggest that recognition of the HLA-B*57:01-TW10 epitope is governed by a 'molecular tension' between the adaptive and innate immune systems.
PubMed: 28218747
DOI: 10.1038/nsmb.3381
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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