8e13: Difference between revisions
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The | ==Structures of HLA-B8E76C loaded with long peptides reveal novel features at the N-terminus of the groove== | ||
<StructureSection load='8e13' size='340' side='right'caption='[[8e13]], [[Resolution|resolution]] 1.37Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8e13]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8E13 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8E13 FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.37Å</td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8e13 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8e13 OCA], [https://pdbe.org/8e13 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8e13 RCSB], [https://www.ebi.ac.uk/pdbsum/8e13 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8e13 ProSAT]</span></td></tr> | |||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/Q5SS57_HUMAN Q5SS57_HUMAN] | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Studies have suggested that MHC class I (MHC I) molecules fluctuate rapidly between numerous conformational states and these motions support peptide sampling. To date, MHC I intermediates are largely uncharacterized experimentally and remain elusive. Here, we present x-ray crystal structures of HLA-B8 loaded with 20mer peptides that show pronounced distortions at the N-terminus of the groove. Long stretches of N-terminal amino acid residues are missing in the electron density maps creating an open-ended groove. Our structures also reveal highly unusual features in MHC I-peptide interaction at the N-terminus of the groove. Molecular dynamics simulations indicate that the complexes have varying degrees of conformational flexibility in a manner consistent with the structures. We suggest that our structures have captured the remarkable molecular dynamics of MHC I-peptide interaction. The visualization of peptide-dependent conformational motions in MHC I is a major step forward in our conceptual understanding of dynamics in high-affinity peptide selection. | |||
Crystal structures of MHC class I complexes reveal the elusive intermediate conformations explored during peptide editing.,Li L, Peng X, Batliwala M, Bouvier M Nat Commun. 2023 Aug 18;14(1):5020. doi: 10.1038/s41467-023-40736-6. PMID:37596268<ref>PMID:37596268</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
[[Category: | </div> | ||
[[Category: Bouvier | <div class="pdbe-citations 8e13" style="background-color:#fffaf0;"></div> | ||
[[Category: Li | == References == | ||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Homo sapiens]] | |||
[[Category: Human immunodeficiency virus 1]] | |||
[[Category: Large Structures]] | |||
[[Category: Bouvier M]] | |||
[[Category: Li L]] | |||
Latest revision as of 09:35, 4 March 2026
Structures of HLA-B8E76C loaded with long peptides reveal novel features at the N-terminus of the groove
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