1n2r

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[[Image:1n2r.jpg|left|200px]]
[[Image:1n2r.jpg|left|200px]]
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{{Structure
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|PDB= 1n2r |SIZE=350|CAPTION= <scene name='initialview01'>1n2r</scene>, resolution 1.7&Aring;
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The line below this paragraph, containing "STRUCTURE_1n2r", creates the "Structure Box" on the page.
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|GENE= HLA-B OR HLAB ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens]), B2M ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])
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{{STRUCTURE_1n2r| PDB=1n2r | SCENE= }}
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|RELATEDENTRY=[[1m6o|1M6O]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1n2r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1n2r OCA], [http://www.ebi.ac.uk/pdbsum/1n2r PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1n2r RCSB]</span>
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'''A natural selected dimorphism in HLA B*44 alters self, peptide reportoire and T cell recognition.'''
'''A natural selected dimorphism in HLA B*44 alters self, peptide reportoire and T cell recognition.'''
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[[Category: Rossjohn, J.]]
[[Category: Rossjohn, J.]]
[[Category: Williams, D S.]]
[[Category: Williams, D S.]]
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[[Category: immune system]]
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[[Category: Immune system]]
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[[Category: mhc i]]
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[[Category: Mhc i]]
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[[Category: signal]]
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[[Category: Signal]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 02:01:10 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 22:24:32 2008''
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Revision as of 23:01, 2 May 2008

Template:STRUCTURE 1n2r

A natural selected dimorphism in HLA B*44 alters self, peptide reportoire and T cell recognition.


Contents

Overview

HLA-B*4402 and B*4403 are naturally occurring MHC class I alleles that are both found at a high frequency in all human populations, and yet they only differ by one residue on the alpha2 helix (B*4402 Asp156-->B*4403 Leu156). CTLs discriminate between HLA-B*4402 and B*4403, and these allotypes stimulate strong mutual allogeneic responses reflecting their known barrier to hemopoeitic stem cell transplantation. Although HLA-B*4402 and B*4403 share >95% of their peptide repertoire, B*4403 presents more unique peptides than B*4402, consistent with the stronger T cell alloreactivity observed toward B*4403 compared with B*4402. Crystal structures of B*4402 and B*4403 show how the polymorphism at position 156 is completely buried and yet alters both the peptide and the heavy chain conformation, relaxing ligand selection by B*4403 compared with B*4402. Thus, the polymorphism between HLA-B*4402 and B*4403 modifies both peptide repertoire and T cell recognition, and is reflected in the paradoxically powerful alloreactivity that occurs across this "minimal" mismatch. The findings suggest that these closely related class I genes are maintained in diverse human populations through their differential impact on the selection of peptide ligands and the T cell repertoire.

Disease

Known disease associated with this structure: Hypoproteinemia, hypercatabolic OMIM:[109700]

About this Structure

1N2R is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

A naturally selected dimorphism within the HLA-B44 supertype alters class I structure, peptide repertoire, and T cell recognition., Macdonald WA, Purcell AW, Mifsud NA, Ely LK, Williams DS, Chang L, Gorman JJ, Clements CS, Kjer-Nielsen L, Koelle DM, Burrows SR, Tait BD, Holdsworth R, Brooks AG, Lovrecz GO, Lu L, Rossjohn J, McCluskey J, J Exp Med. 2003 Sep 1;198(5):679-91. Epub 2003 Aug 25. PMID:12939341 Page seeded by OCA on Sat May 3 02:01:10 2008

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