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[[Image:1sjh.gif|left|200px]]<br />
<applet load="1sjh" size="450" color="white" frame="true" align="right" spinBox="true"
caption="1sjh, resolution 2.25&Aring;" />
'''HLA-DR1 complexed with a 13 residue HIV capsid peptide'''<br />


==Overview==
==HLA-DR1 complexed with a 13 residue HIV capsid peptide==
T cells generally recognize peptide antigens bound to MHC proteins through, contacts with residues found within or immediately flanking the seven- to, nine-residue sequence accommodated in the MHC peptide-binding groove., However, some T cells require peptide residues outside this region for, activation, the structural basis for which is unknown. Here, we have, investigated a HIV Gag-specific T cell clone that requires an unusually, long peptide antigen for activation. The crystal structure of a minimally, antigenic 16-mer bound to HLA-DR1 shows that the peptide C-terminal region, bends sharply into a hairpin turn as it exits the binding site, orienting, peptide residues outside the MHC-binding region in position to interact, with a T cell receptor. Peptide truncation and substitution studies show, that both the hairpin turn and the extreme C-terminal residues are, required for T cell activation. These results demonstrate a previously, unrecognized mode of MHC-peptide-T cell receptor interaction.
<StructureSection load='1sjh' size='340' side='right'caption='[[1sjh]], [[Resolution|resolution]] 2.25&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1sjh]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens], [https://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SJH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1SJH FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.25&#8491;</td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=1sjh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1sjh OCA], [https://pdbe.org/1sjh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1sjh RCSB], [https://www.ebi.ac.uk/pdbsum/1sjh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1sjh ProSAT]</span></td></tr>
</table>
== Function ==
[https://www.uniprot.org/uniprot/ENTC3_STAAU ENTC3_STAAU] Staphylococcal enterotoxins cause the intoxication staphylococcal food poisoning syndrome. The illness is characterized by high fever, hypotension, diarrhea, shock, and in some cases death.
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
Check<jmol>
  <jmolCheckbox>
    <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/sj/1sjh_consurf.spt"</scriptWhenChecked>
    <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.spt</scriptWhenUnchecked>
    <text>to colour the structure by Evolutionary Conservation</text>
  </jmolCheckbox>
</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=1sjh ConSurf].
<div style="clear:both"></div>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
T cells generally recognize peptide antigens bound to MHC proteins through contacts with residues found within or immediately flanking the seven- to nine-residue sequence accommodated in the MHC peptide-binding groove. However, some T cells require peptide residues outside this region for activation, the structural basis for which is unknown. Here, we have investigated a HIV Gag-specific T cell clone that requires an unusually long peptide antigen for activation. The crystal structure of a minimally antigenic 16-mer bound to HLA-DR1 shows that the peptide C-terminal region bends sharply into a hairpin turn as it exits the binding site, orienting peptide residues outside the MHC-binding region in position to interact with a T cell receptor. Peptide truncation and substitution studies show that both the hairpin turn and the extreme C-terminal residues are required for T cell activation. These results demonstrate a previously unrecognized mode of MHC-peptide-T cell receptor interaction.


==About this Structure==
A hairpin turn in a class II MHC-bound peptide orients residues outside the binding groove for T cell recognition.,Zavala-Ruiz Z, Strug I, Walker BD, Norris PJ, Stern LJ Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13279-84. Epub 2004 Aug 26. PMID:15331779<ref>PMID:15331779</ref>
1SJH is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Staphylococcus_aureus Staphylococcus aureus]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SJH OCA].


==Reference==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
A hairpin turn in a class II MHC-bound peptide orients residues outside the binding groove for T cell recognition., Zavala-Ruiz Z, Strug I, Walker BD, Norris PJ, Stern LJ, Proc Natl Acad Sci U S A. 2004 Sep 7;101(36):13279-84. Epub 2004 Aug 26. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15331779 15331779]
</div>
<div class="pdbe-citations 1sjh" style="background-color:#fffaf0;"></div>
 
==See Also==
*[[MHC 3D structures|MHC 3D structures]]
*[[MHC II 3D structures|MHC II 3D structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Protein complex]]
[[Category: Large Structures]]
[[Category: Staphylococcus aureus]]
[[Category: Staphylococcus aureus]]
[[Category: Norris, P.J.]]
[[Category: Synthetic construct]]
[[Category: Stern, L.J.]]
[[Category: Norris PJ]]
[[Category: Strug, I.]]
[[Category: Stern LJ]]
[[Category: Walker, B.D.]]
[[Category: Strug I]]
[[Category: Zavala-Ruiz, Z.]]
[[Category: Walker BD]]
[[Category: antigen]]
[[Category: Zavala-Ruiz Z]]
[[Category: capsid]]
[[Category: gag]]
[[Category: hiv-1]]
[[Category: hla-dr1]]
[[Category: major histocompatibility protein complex]]
[[Category: mhc class ii]]
[[Category: peptide]]
[[Category: superantigen]]
 
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