5TW2
Structure of mouse CD1d with bound alpha-galactosylsphingamide JG168
Summary for 5TW2
Entry DOI | 10.2210/pdb5tw2/pdb |
Related | 1Z5L 5TW5 |
Descriptor | Antigen-presenting glycoprotein CD1d1, Beta-2-microglobulin, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose, ... (7 entities in total) |
Functional Keywords | mhc fold, antigen-presentation, glycolipid, t cells, immune system-inhibitor complex, immune system/inhibitor |
Biological source | Mus musculus (Mouse) More |
Total number of polymer chains | 2 |
Total formula weight | 45996.02 |
Authors | Zajonc, D.M.,Wang, J. (deposition date: 2016-11-11, release date: 2017-09-20, Last modification date: 2024-11-20) |
Primary citation | Guillaume, J.,Wang, J.,Janssens, J.,Remesh, S.G.,Risseeuw, M.D.P.,Decruy, T.,Froeyen, M.,Elewaut, D.,Zajonc, D.M.,Calenbergh, S.V. Galactosylsphingamides: new alpha-GalCer analogues to probe the F'-pocket of CD1d. Sci Rep, 7:4276-4276, 2017 Cited by PubMed Abstract: Invariant Natural Killer T-cells (iNKT-cells) are an attractive target for immune response modulation, as upon CD1d-mediated stimulation with KRN7000, a synthetic α-galactosylceramide, they produce a vast amount of cytokines. Here we present a synthesis that allows swift modification of the phytosphingosine side chain by amidation of an advanced methyl ester precursor. The resulting KRN7000 derivatives, termed α-galactosylsphingamides, were evaluated for their capacity to stimulate iNKT-cells. While introduction of the amide-motif in the phytosphingosine chain is tolerated for CD1d binding and TCR recognition, the studied α-galactosylsphingamides showed compromised antigenic properties. PubMed: 28655912DOI: 10.1038/s41598-017-04461-7 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.75 Å) |
Structure validation
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