8wsq
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==A protective human antibody against respiratory syncytial virus by targeting a prefusion epitope across sites IV and V of the viral fusion glycoprotein.== | |
| - | + | <StructureSection load='8wsq' size='340' side='right'caption='[[8wsq]], [[Resolution|resolution]] 2.90Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8wsq]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Respiratory_syncytial_virus Respiratory syncytial virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8WSQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8WSQ 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]] 2.9Å</td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8wsq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8wsq OCA], [https://pdbe.org/8wsq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8wsq RCSB], [https://www.ebi.ac.uk/pdbsum/8wsq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8wsq ProSAT]</span></td></tr> |
| - | [[Category: Chai | + | </table> |
| - | [[Category: Xu | + | == Function == |
| + | [https://www.uniprot.org/uniprot/C3UPB8_9MONO C3UPB8_9MONO] | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Respiratory syncytial virus]] | ||
| + | [[Category: Chai Y]] | ||
| + | [[Category: Xu SY]] | ||
Revision as of 07:45, 15 November 2023
A protective human antibody against respiratory syncytial virus by targeting a prefusion epitope across sites IV and V of the viral fusion glycoprotein.
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