1sjh: Difference between revisions

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[[Image:1sjh.gif|left|200px]]
[[Image:1sjh.gif|left|200px]]


{{Structure
<!--
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|SITE=
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|GENE= HLA-DRA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), HLA-DRB1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), ENTC3, SAV2009, SA1817 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1280 Staphylococcus aureus])
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|DOMAIN=
{{STRUCTURE_1sjh| PDB=1sjh  | SCENE= }}  
|RELATEDENTRY=[[1klu|1KLU]], [[1pyw|1PYW]], [[1sje|1SJE]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1sjh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1sjh OCA], [http://www.ebi.ac.uk/pdbsum/1sjh PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1sjh RCSB]</span>
}}


'''HLA-DR1 complexed with a 13 residue HIV capsid peptide'''
'''HLA-DR1 complexed with a 13 residue HIV capsid peptide'''
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[[Category: Walker, B D.]]
[[Category: Walker, B D.]]
[[Category: Zavala-Ruiz, Z.]]
[[Category: Zavala-Ruiz, Z.]]
[[Category: antigen]]
[[Category: Antigen]]
[[Category: capsid]]
[[Category: Capsid]]
[[Category: gag]]
[[Category: Gag]]
[[Category: hiv-1]]
[[Category: Hiv-1]]
[[Category: hla-dr1]]
[[Category: Hla-dr1]]
[[Category: major histocompatibility protein complex]]
[[Category: Major histocompatibility protein complex]]
[[Category: mhc class ii]]
[[Category: Mhc class ii]]
[[Category: peptide]]
[[Category: Peptide]]
[[Category: superantigen]]
[[Category: Superantigen]]
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May  3 08:46:48 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:42:53 2008''

Revision as of 08:46, 3 May 2008

File:1sjh.gif

Template:STRUCTURE 1sjh

HLA-DR1 complexed with a 13 residue HIV capsid peptide


OverviewOverview

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 StructureAbout this Structure

1SJH is a Protein complex structure of sequences from Homo sapiens and Staphylococcus aureus. Full crystallographic information is available from OCA.

ReferenceReference

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 Page seeded by OCA on Sat May 3 08:46:48 2008

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