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7y6v

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'''Unreleased structure'''
 
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The entry 7y6v is ON HOLD
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==Symmetry-expanded and locally refined protomer structure of IPEC-J2 cell-derived PEDV PT52 S with a CTD-open conformation==
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<StructureSection load='7y6v' size='340' side='right'caption='[[7y6v]], [[Resolution|resolution]] 3.30&Aring;' scene=''>
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Authors: Hsu, S.T.D., Draczkowski, P., Wang, Y.S.
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== Structural highlights ==
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<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>
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Description: Symmetry-expanded and locally refined protomer structure of IPEC-J2 cell-derived PEDV PT52 S with a CTD-open conformation
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</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>
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[[Category: Unreleased Structures]]
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<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>
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[[Category: Wang, Y.S]]
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</table>
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[[Category: Hsu, S.T.D]]
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== Function ==
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[[Category: Draczkowski, P]]
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[[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]
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Porcine epidemic diarrhea virus]]
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[[Category: Draczkowski P]]
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[[Category: Hsu STD]]
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[[Category: Wang YS]]

Current revision

Symmetry-expanded and locally refined protomer structure of IPEC-J2 cell-derived PEDV PT52 S with a CTD-open conformation

PDB ID 7y6v

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