1juf

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[[Image:1juf.jpg|left|200px]]
[[Image:1juf.jpg|left|200px]]
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{{Structure
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|PDB= 1juf |SIZE=350|CAPTION= <scene name='initialview01'>1juf</scene>, resolution 2.00&Aring;
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The line below this paragraph, containing "STRUCTURE_1juf", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|GENE= H2-D ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 Mus musculus]), beta-2-microglobulin ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 Mus musculus]), H13 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 Mus musculus])
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|DOMAIN=
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{{STRUCTURE_1juf| PDB=1juf | SCENE= }}
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|RELATEDENTRY=[[1inq|1INQ]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1juf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1juf OCA], [http://www.ebi.ac.uk/pdbsum/1juf PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1juf RCSB]</span>
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'''Structure of Minor Histocompatibility Antigen peptide, H13b, complexed to H2-Db'''
'''Structure of Minor Histocompatibility Antigen peptide, H13b, complexed to H2-Db'''
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[[Category: Tilley, D.]]
[[Category: Tilley, D.]]
[[Category: Villaflor, G.]]
[[Category: Villaflor, G.]]
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[[Category: h13]]
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[[Category: H13]]
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[[Category: h2-db]]
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[[Category: H2-db]]
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[[Category: mhc class-i]]
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[[Category: Mhc class-i]]
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[[Category: minor histocompatibility antigen]]
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[[Category: Minor histocompatibility antigen]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 21:56:18 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 21:39:12 2008''
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Revision as of 18:56, 2 May 2008

Template:STRUCTURE 1juf

Structure of Minor Histocompatibility Antigen peptide, H13b, complexed to H2-Db


Overview

The mouse H13 minor histocompatibility (H) Ag, originally detected as a barrier to allograft transplants, is remarkable in that rejection is a consequence of an extremely subtle interchange, P4(Val/Ile), in a nonamer H2-D(b)-bound peptide. Moreover, H13 peptides lack the canonical P5(Asn) central anchor residue normally considered important for forming a peptide/MHC complex. To understand how these noncanonical peptide pMHC complexes form physiologically active TCR ligands, crystal structures of allelic H13 pD(b) complexes and a P5(Asn) anchored pD(b) analog were solved to high resolution. The structures show that the basis of TCRs to distinguish self from nonself H13 peptides is their ability to distinguish a single solvent-exposed methyl group. In addition, the structures demonstrate that there is no need for H13 peptides to derive any stabilization from interactions within the central C pocket to generate fully functional pMHC complexes. These results provide a structural explanation for a classical non-MHC-encoded H Ag, and they call into question the requirement for contact between anchor residues and the major MHC binding pockets in vaccine design.

About this Structure

1JUF is a Protein complex structure of sequences from Mus musculus. Full crystallographic information is available from OCA.

Reference

How H13 histocompatibility peptides differing by a single methyl group and lacking conventional MHC binding anchor motifs determine self-nonself discrimination., Ostrov DA, Roden MM, Shi W, Palmieri E, Christianson GJ, Mendoza L, Villaflor G, Tilley D, Shastri N, Grey H, Almo SC, Roopenian D, Nathenson SG, J Immunol. 2002 Jan 1;168(1):283-9. PMID:11751972 Page seeded by OCA on Fri May 2 21:56:18 2008

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