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4EI5

Crystal Structure of XV19 TCR in complex with CD1d-sulfatide C24:1

Summary for 4EI5
Entry DOI10.2210/pdb4ei5/pdb
Related2AKR 4EI6
DescriptorAntigen-presenting glycoprotein CD1d1, (15Z)-N-((1S,2R,3E)-2-HYDROXY-1-{[(3-O-SULFO-BETA-D-GALACTOPYRANOSYL)OXY]METHYL}HEPTADEC-3-ENYL)TETRACOS-15-ENAMIDE, Beta-2-microglobulin, ... (10 entities in total)
Functional Keywordssulfatide, lipid, cd1d, nkt typeii, tcr, immune system
Biological sourceMus musculus (mouse)
More
Total number of polymer chains8
Total formula weight199821.14
Authors
Patel, O.,Gras, S.,Rossjohn, J. (deposition date: 2012-04-04, release date: 2012-07-25, Last modification date: 2023-09-13)
Primary citationPatel, O.,Pellicci, D.G.,Gras, S.,Sandoval-Romero, M.L.,Uldrich, A.P.,Mallevaey, T.,Clarke, A.J.,Le Nours, J.,Theodossis, A.,Cardell, S.L.,Gapin, L.,Godfrey, D.I.,Rossjohn, J.
Recognition of CD1d-sulfatide mediated by a type II natural killer T cell antigen receptor.
Nat.Immunol., 13:857-863, 2012
Cited by
PubMed Abstract: Natural killer T cells (NKT cells) are divided into type I and type II subsets on the basis of differences in their T cell antigen receptor (TCR) repertoire and CD1d-antigen specificity. Although the mode by which type I NKT cell TCRs recognize CD1d-antigen has been established, how type II NKT cell TCRs engage CD1d-antigen is unknown. Here we provide a basis for how a type II NKT cell TCR, XV19, recognized CD1d-sulfatide. The XV19 TCR bound orthogonally above the A' pocket of CD1d, in contrast to the parallel docking of type I NKT cell TCRs over the F' pocket of CD1d. At the XV19 TCR-CD1d-sulfatide interface, the TCRα and TCRβ chains sat centrally on CD1d, where the malleable CDR3 loops dominated interactions with CD1d-sulfatide. Accordingly, we highlight the diverse mechanisms by which NKT cell TCRs can bind CD1d and account for the distinct antigen specificity of type II NKT cells.
PubMed: 22820603
DOI: 10.1038/ni.2372
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.1 Å)
Structure validation

226707

數據於2024-10-30公開中

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