7y6v
From Proteopedia
(Difference between revisions)
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==Symmetry-expanded and locally refined protomer structure of IPEC-J2 cell-derived PEDV PT52 S with a CTD-open conformation== | ==Symmetry-expanded and locally refined protomer structure of IPEC-J2 cell-derived PEDV PT52 S with a CTD-open conformation== | ||
- | <StructureSection load='7y6v' size='340' side='right'caption='[[7y6v]]' scene=''> | + | <StructureSection load='7y6v' size='340' side='right'caption='[[7y6v]], [[Resolution|resolution]] 3.30Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7Y6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7Y6V FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7y6v]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Porcine_epidemic_diarrhea_virus Porcine epidemic diarrhea virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7Y6V OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7Y6V 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=7y6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7y6v OCA], [https://pdbe.org/7y6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7y6v RCSB], [https://www.ebi.ac.uk/pdbsum/7y6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7y6v ProSAT]</span></td></tr> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=FUC:ALPHA-L-FUCOSE'>FUC</scene>, <scene name='pdbligand=MAN:ALPHA-D-MANNOSE'>MAN</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></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=7y6v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7y6v OCA], [https://pdbe.org/7y6v PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7y6v RCSB], [https://www.ebi.ac.uk/pdbsum/7y6v PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7y6v ProSAT]</span></td></tr> | ||
</table> | </table> | ||
+ | == Function == | ||
+ | [[https://www.uniprot.org/uniprot/A0A1Y0DD46_9ALPC A0A1Y0DD46_9ALPC]] S1 region attaches the virion to the cell membrane by interacting with the host receptor, initiating the infection. Binding to the receptor probably induces conformational changes in the S glycoprotein unmasking the fusion peptide of S2 region and activating membranes fusion. S2 region belongs to the class I viral fusion protein. Under the current model, the protein has at least 3 conformational states: pre-fusion native state, pre-hairpin intermediate state, and post-fusion hairpin state. During viral and target cell membrane fusion, the coiled coil regions (heptad repeats) regions assume a trimer-of-hairpins structure, positioning the fusion peptide in close proximity to the C-terminal region of the ectodomain. The formation of this structure appears to drive apposition and subsequent fusion of viral and target cell membranes.[HAMAP-Rule:MF_04200] | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
+ | [[Category: Porcine epidemic diarrhea virus]] | ||
[[Category: Draczkowski P]] | [[Category: Draczkowski P]] | ||
[[Category: Hsu STD]] | [[Category: Hsu STD]] | ||
[[Category: Wang YS]] | [[Category: Wang YS]] |
Revision as of 03:24, 8 September 2022
Symmetry-expanded and locally refined protomer structure of IPEC-J2 cell-derived PEDV PT52 S with a CTD-open conformation
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