This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.


Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


2cik

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
[[Image:2cik.jpg|left|200px]]
[[Image:2cik.jpg|left|200px]]
-
{{Structure
+
<!--
-
|PDB= 2cik |SIZE=350|CAPTION= <scene name='initialview01'>2cik</scene>, resolution 1.75&Aring;
+
The line below this paragraph, containing "STRUCTURE_2cik", creates the "Structure Box" on the page.
-
|SITE= <scene name='pdbsite=AC1:Gol+Binding+Site+For+Chain+B'>AC1</scene>
+
You may change the PDB parameter (which sets the PDB file loaded into the applet)
-
|LIGAND= <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>
+
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
-
|ACTIVITY=
+
or leave the SCENE parameter empty for the default display.
-
|GENE=
+
-->
-
|DOMAIN=
+
{{STRUCTURE_2cik| PDB=2cik | SCENE= }}
-
|RELATEDENTRY=
+
-
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2cik FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2cik OCA], [http://www.ebi.ac.uk/pdbsum/2cik PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2cik RCSB]</span>
+
-
}}
+
'''INSIGHTS INTO CROSSREACTIVITY IN HUMAN ALLORECOGNITION: THE STRUCTURE OF HLA-B35011 PRESENTING AN EPITOPE DERIVED FROM CYTOCHROME P450.'''
'''INSIGHTS INTO CROSSREACTIVITY IN HUMAN ALLORECOGNITION: THE STRUCTURE OF HLA-B35011 PRESENTING AN EPITOPE DERIVED FROM CYTOCHROME P450.'''
Line 31: Line 28:
[[Category: Jones, E Y.]]
[[Category: Jones, E Y.]]
[[Category: Peterson, N A.]]
[[Category: Peterson, N A.]]
-
[[Category: allo-ligand]]
+
[[Category: Allo-ligand]]
-
[[Category: antigen/peptide complex]]
+
[[Category: Antigen/peptide complex]]
-
[[Category: ebv]]
+
[[Category: Ebv]]
-
[[Category: glycoprotein]]
+
[[Category: Glycoprotein]]
-
[[Category: hla]]
+
[[Category: Hla]]
-
[[Category: hla-b3501]]
+
[[Category: Hla-b3501]]
-
[[Category: human]]
+
[[Category: Human]]
-
[[Category: immune response]]
+
[[Category: Immune response]]
-
[[Category: immunoglobulin domain]]
+
[[Category: Immunoglobulin domain]]
-
[[Category: major histocompatibility antigen]]
+
[[Category: Major histocompatibility antigen]]
-
[[Category: membrane]]
+
[[Category: Membrane]]
-
[[Category: mhc]]
+
[[Category: Mhc]]
-
[[Category: mhc i]]
+
[[Category: Mhc i]]
-
[[Category: polymorphism]]
+
[[Category: Polymorphism]]
-
[[Category: pyrrolidone carboxylic acid]]
+
[[Category: Pyrrolidone carboxylic acid]]
-
[[Category: transmembrane]]
+
[[Category: Transmembrane]]
-
 
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 22:13:32 2008''
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:22:01 2008''
+

Revision as of 19:13, 3 May 2008

Template:STRUCTURE 2cik

INSIGHTS INTO CROSSREACTIVITY IN HUMAN ALLORECOGNITION: THE STRUCTURE OF HLA-B35011 PRESENTING AN EPITOPE DERIVED FROM CYTOCHROME P450.


Overview

Virus-specific T cell populations have been implicated in allo-recognition. The subdominant T cell receptor JL12 recognizes both HLA-B*0801 presenting the Epstein-Barr virus-derived peptide FLRGRAYGL and also HLA-B*3501 presenting the cytochrome p450 self peptide KPIVVLHGY. This cross-reactivity could promote the rejection of HLA-B*3501-positive cells in Epstein-Barr virus-exposed HLA-B*0801 recipients. LC13, the dominant TCR against the HLA-B*0801:FLRGRAYGL complex, fails to recognize HLA-B*3501:KPIVVLHGY. We report the 1.75-Angstrom resolution crystal structure of the human allo-ligand HLA-B*3501:KPIVVLHGY. Similarities between this structure and that of HLA-B*0801:FLRGRAYGL may facilitate cross-recognition by JL12. Moreover, the elevated peptide position in HLA-B*3501:KPIVVLHGY would provide steric hindrance to LC13, preventing it from interacting in the manner in which it interacts with HLA-B*0801:FLRGRAYGL. These findings are relevant to understanding the basis of T cell cross-reactivity in allo-recognition, optimal transplant donor-recipient matching and developing specific molecular inhibitors of allo-recognition.

About this Structure

2CIK is a Protein complex structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.

Reference

The structure of the human allo-ligand HLA-B*3501 in complex with a cytochrome p450 peptide: steric hindrance influences TCR allo-recognition., Hourigan CS, Harkiolaki M, Peterson NA, Bell JI, Jones EY, O'Callaghan CA, Eur J Immunol. 2006 Dec;36(12):3288-93. PMID:17109469 Page seeded by OCA on Sat May 3 22:13:32 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools