2yhf: Difference between revisions
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<StructureSection load='2yhf' size='340' side='right'caption='[[2yhf]], [[Resolution|resolution]] 1.90Å' scene=''> | <StructureSection load='2yhf' size='340' side='right'caption='[[2yhf]], [[Resolution|resolution]] 1.90Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2yhf]] is a 9 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[2yhf]] is a 9 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2YHF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2YHF FirstGlance]. <br> | ||
</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=2yhf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2yhf OCA], [https://pdbe.org/2yhf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2yhf RCSB], [https://www.ebi.ac.uk/pdbsum/2yhf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2yhf ProSAT]</span></td></tr> | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9Å</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=2yhf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2yhf OCA], [https://pdbe.org/2yhf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2yhf RCSB], [https://www.ebi.ac.uk/pdbsum/2yhf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2yhf ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/CLC5A_HUMAN CLC5A_HUMAN] Functions as a positive regulator of osteoclastogenesis. Cell surface receptor that signals via TYROBP. Regulates inflammatory responses. Acts as a key regulator of synovial injury and bone erosion during autoimmune joint inflammation (By similarity). Critical macrophage receptor for dengue virus serotypes 1-4. The binding of dengue virus to CLEC5A triggers signaling through the phosphylation of TYROBP, this interaction does not result in viral entry, but stimulates proinflammatory cytokine release.<ref>PMID:10449773</ref> <ref>PMID:18496526</ref> | |||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Hall BA]] | |||
[[Category: Hall | [[Category: Lebedev AA]] | ||
[[Category: Lebedev | [[Category: Murshudov GM]] | ||
[[Category: Murshudov | [[Category: O'Callaghan CA]] | ||
[[Category: | [[Category: Vagin AA]] | ||
[[Category: | [[Category: Watson AA]] | ||
[[Category: | |||
Latest revision as of 13:52, 20 December 2023
1.9 Angstrom Crystal Structure of CLEC5A1.9 Angstrom Crystal Structure of CLEC5A
Structural highlights
FunctionCLC5A_HUMAN Functions as a positive regulator of osteoclastogenesis. Cell surface receptor that signals via TYROBP. Regulates inflammatory responses. Acts as a key regulator of synovial injury and bone erosion during autoimmune joint inflammation (By similarity). Critical macrophage receptor for dengue virus serotypes 1-4. The binding of dengue virus to CLEC5A triggers signaling through the phosphylation of TYROBP, this interaction does not result in viral entry, but stimulates proinflammatory cytokine release.[1] [2] Publication Abstract from PubMedThe human C-type lectin-like molecule CLEC5A is a critical macrophage receptor for dengue virus. Binding of dengue virus to CLEC5A triggers signaling through the associated adapter molecule DAP12, stimulating proinflammatory cytokine release. We crystallized an informative ensemble of CLEC5A structural isoforms at 1.9 Angstrom resolution, and demonstrate how an on-off extension to a beta-sheet acts as a binary switch regulating the flexibility of the molecule. This structural information together with molecular dynamics simulations, suggests a mechanism whereby extracellular events may be transmitted through the membrane and influence DAP12 signaling. We demonstrate that CLEC5A is homodimeric and binds to dengue virus serotypes 1-4. Using blotting experiments, surface analyses and docking studies, we investigate the interaction of CLEC5A with dengue virus, mannose, fucose and associated sugars and highlight three distinct potential ligand binding sites. This study provides a rational foundation for understanding the dengue virus-macrophage interaction and the role of CLEC5A in dengue virus-induced lethal disease. Structural flexibility of the macrophage dengue virus receptor CLEC5A: Implications for ligand binding and signaling.,Watson AA, Lebedev AA, Hall BA, Fenton-May AE, Vagin AA, Dejnirattisai W, Felce J, Mongkolsapaya J, Palma AS, Liu Y, Feizi T, Screaton GR, Murshudov GN, O'Callaghan CA J Biol Chem. 2011 May 12. PMID:21566123[3] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. References
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