3tjh: Difference between revisions
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==42F3-p3A1/H2-Ld complex== | ==42F3-p3A1/H2-Ld complex== | ||
<StructureSection load='3tjh' size='340' side='right' caption='[[3tjh]], [[Resolution|resolution]] 2.12Å' scene=''> | <StructureSection load='3tjh' size='340' side='right' caption='[[3tjh]], [[Resolution|resolution]] 2.12Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[3tjh]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice | <table><tr><td colspan='2'>[[3tjh]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Lk3_transgenic_mice Lk3 transgenic mice]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3TJH OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3TJH FirstGlance]. <br> | ||
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2oi9|2oi9]], [[3tf7|3tf7]], [[3tfk|3tfk]], [[3tpu|3tpu]]</td></tr> | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[2oi9|2oi9]], [[3tf7|3tf7]], [[3tfk|3tfk]], [[3tpu|3tpu]]</td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3tjh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3tjh OCA], [http://www.rcsb.org/pdb/explore.do?structureId=3tjh RCSB], [http://www.ebi.ac.uk/pdbsum/3tjh PDBsum]</span></td></tr> | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=3tjh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3tjh OCA], [http://pdbe.org/3tjh PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=3tjh RCSB], [http://www.ebi.ac.uk/pdbsum/3tjh PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=3tjh ProSAT]</span></td></tr> | ||
</table> | </table> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | ||
</div> | </div> | ||
<div class="pdbe-citations 3tjh" style="background-color:#fffaf0;"></div> | |||
== References == | == References == | ||
<references/> | <references/> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Lk3 transgenic mice]] | [[Category: Lk3 transgenic mice]] | ||
[[Category: Adams, J J]] | [[Category: Adams, J J]] | ||
[[Category: Garcia, K C]] | [[Category: Garcia, K C]] | ||
Revision as of 19:49, 11 August 2016
42F3-p3A1/H2-Ld complex42F3-p3A1/H2-Ld complex
Structural highlights
Publication Abstract from PubMedT cell receptor (TCR) engagement of peptide-major histocompatibility complex (pMHC) is essential to adaptive immunity, but it is unknown whether TCR signaling responses are influenced by the binding topology of the TCR-peptide-MHC complex. We developed yeast-displayed pMHC libraries that enabled us to identify new peptide sequences reactive with a single TCR. Structural analysis showed that four peptides bound to the TCR with distinct 3D and 2D affinities using entirely different binding chemistries. Three of the peptides that shared a common docking mode, where key TCR-MHC germline interactions are preserved, induced TCR signaling. The fourth peptide failed to induce signaling and was recognized in a substantially different TCR-MHC binding mode that apparently exceeded geometric tolerances compatible with signaling. We suggest that the stereotypical TCR-MHC docking paradigm evolved from productive signaling geometries and that TCR signaling can be modulated by peptides that are recognized in alternative TCR-pMHC binding orientations. T Cell Receptor Signaling Is Limited by Docking Geometry to Peptide-Major Histocompatibility Complex.,Adams JJ, Narayanan S, Liu B, Birnbaum ME, Kruse AC, Bowerman NA, Chen W, Levin AM, Connolly JM, Zhu C, Kranz DM, Garcia KC Immunity. 2011 Nov 16. PMID:22101157[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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