3bzf: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
New page: left|200px <!-- The line below this paragraph, containing "STRUCTURE_3bzf", creates the "Structure Box" on the page. You may change the PDB parameter (which sets the PD...
 
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
[[Image:3bzf.jpg|left|200px]]
{{Seed}}
[[Image:3bzf.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_3bzf|  PDB=3bzf  |  SCENE=  }}  
{{STRUCTURE_3bzf|  PDB=3bzf  |  SCENE=  }}  


'''The human non-classical major histocompatibility complex molecule HLA-E'''
===The human non-classical major histocompatibility complex molecule HLA-E===




==Overview==
<!--  
Human leukocyte antigen (HLA)-E is a non-classical major histocompatibility complex class I molecule that binds peptides derived from the leader sequences of other HLA class I molecules. Natural killer cell recognition of these HLA-E molecules, via the CD94-NKG2 natural killer family, represents a central innate mechanism for monitoring major histocompatibility complex expression levels within a cell. The leader sequence-derived peptides bound to HLA-E exhibit very limited polymorphism, yet subtle differences affect the recognition of HLA-E by the CD94-NKG2 receptors. To better understand the basis for this peptide-specific recognition, we determined the structure of HLA-E in complex with two leader peptides, namely, HLA-Cw*07 (VMAPRALLL), which is poorly recognised by CD94-NKG2 receptors, and HLA-G*01 (VMAPRTLFL), a high-affinity ligand of CD94-NKG2 receptors. A comparison of these structures, both of which were determined to 2.5-A resolution, revealed that allotypic variations in the bound leader sequences do not result in conformational changes in the HLA-E heavy chain, although subtle changes in the conformation of the peptide within the binding groove of HLA-E were evident. Accordingly, our data indicate that the CD94-NKG2 receptors interact with HLA-E in a manner that maximises the ability of the receptors to discriminate between subtle changes in both the sequence and conformation of peptides bound to HLA-E.
The line below this paragraph, {{ABSTRACT_PUBMED_18339401}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 18339401 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_18339401}}


==About this Structure==
==About this Structure==
Line 47: Line 51:
[[Category: Transmembrane]]
[[Category: Transmembrane]]
[[Category: Ubl conjugation]]
[[Category: Ubl conjugation]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Apr 30 13:34:21 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 16:39:38 2008''