9hi7

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Current revision (05:29, 23 April 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9hi7 is ON HOLD until Paper Publication
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==Structure of MC.7.G5 T cell receptor in complex with MR1 R9H==
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<StructureSection load='9hi7' size='340' side='right'caption='[[9hi7]], [[Resolution|resolution]] 2.81&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9hi7]] is a 8 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9HI7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9HI7 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.81&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9hi7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9hi7 OCA], [https://pdbe.org/9hi7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9hi7 RCSB], [https://www.ebi.ac.uk/pdbsum/9hi7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9hi7 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/HMR1_HUMAN HMR1_HUMAN] Has antigen presentation function. Involved in the development and expansion of a small population of T-cells expressing an invariant T-cell receptor alpha chain called mucosal-associated invariant T-cells (MAIT). MAIT cells are preferentially located in the gut lamina propria and therefore may be involved in monitoring commensal flora or serve as a distress signal. Expression and MAIT cell recognition seem to be ligand-dependent.<ref>PMID:12794138</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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INTRODUCTION: The MHC-class-I-related molecule MR1 presents small metabolites of microbial and self-origin to T cells bearing semi-invariant or variant T cell receptors. One such T cell receptor, MC.7.G5, was previously shown to confer broad MR1-restricted reactivity to tumor cells but not normal cells, sparking interest in the development of non-MHC-restricted immunotherapy approaches. METHODS/RESULTS: Here we provide cellular, biophysical, and crystallographic evidence that the MC.7.G5 TCR does not have pan-cancer specificity but is restricted to a rare allomorph of MR1, bearing the R9H mutation. DISCUSSION: Our results underscore the importance of in-depth characterization of MR1-reactive TCRs against targets expressing the full repertoire of MR1 allomorphs.
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Authors:
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Molecular basis underpinning MR1 allomorph recognition by an MR1-restricted T cell receptor.,Suckling RJ, Pamukcu C, Simmons RA, Fonseca D, Grant E, Harrison R, Shaikh SA, Khanolkar RC, Ghadbane H, Creese A, Hock M, Gligoris TG, Lepore M, Karuppiah V, Salio M Front Immunol. 2025 Mar 26;16:1547664. doi: 10.3389/fimmu.2025.1547664. , eCollection 2025. PMID:40207221<ref>PMID:40207221</ref>
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Description:
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 9hi7" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Karuppiah V]]

Current revision

Structure of MC.7.G5 T cell receptor in complex with MR1 R9H

PDB ID 9hi7

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