7coe

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'''Unreleased structure'''
 
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The entry 7coe is ON HOLD until Aug 04 2022
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==Crystal structure of Receptor binding domain of MERS-CoV and KNIH90-F1 Fab complex==
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<StructureSection load='7coe' size='340' side='right'caption='[[7coe]], [[Resolution|resolution]] 2.05&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[7coe]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Middle_East_respiratory_syndrome-related_coronavirus Middle East respiratory syndrome-related coronavirus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7COE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7COE FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.05&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr>
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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=7coe FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7coe OCA], [https://pdbe.org/7coe PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7coe RCSB], [https://www.ebi.ac.uk/pdbsum/7coe PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7coe ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/SPIKE_MERS1 SPIKE_MERS1] Attaches the virion to the cell membrane by interacting with host receptor, initiating the infection (By similarity). Interacts with host DPP4 to mediate virla entry.[HAMAP-Rule:MF_04099]<ref>PMID:23486063</ref> Mediates fusion of the virion and cellular membranes by acting as a class I viral fusion protein. Under the current model, the protein has at least three 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) 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_04099] Acts as a viral fusion peptide which is unmasked following S2 cleavage occurring upon virus endocytosis.[HAMAP-Rule:MF_04099]
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Authors: Lee, J.Y., Song, J.Y., Lee, H.S., Hong, E., Jang, T.H.
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==See Also==
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*[[Antibody 3D structures|Antibody 3D structures]]
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Description: Crystal structure of Receptor binding domain of MERS-CoV and KNIH90-F1 Fab complex
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Song, J.Y]]
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__TOC__
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[[Category: Lee, J.Y]]
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</StructureSection>
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[[Category: Lee, H.S]]
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[[Category: Homo sapiens]]
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[[Category: Hong, E]]
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[[Category: Large Structures]]
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[[Category: Jang, T.H]]
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[[Category: Middle East respiratory syndrome-related coronavirus]]
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[[Category: Hong E]]
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[[Category: Jang TH]]
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[[Category: Lee HS]]
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[[Category: Lee JY]]
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[[Category: Song JY]]

Current revision

Crystal structure of Receptor binding domain of MERS-CoV and KNIH90-F1 Fab complex

PDB ID 7coe

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