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6crz
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==SARS Spike Glycoprotein, Trypsin-cleaved, Stabilized variant, C3 symmetry== | |
| - | + | <StructureSection load='6crz' size='340' side='right' caption='[[6crz]], [[Resolution|resolution]] 3.30Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[6crz]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CRZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6CRZ FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=MAN:ALPHA-D-MANNOSE'>MAN</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6crz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6crz OCA], [http://pdbe.org/6crz PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6crz RCSB], [http://www.ebi.ac.uk/pdbsum/6crz PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6crz ProSAT]</span></td></tr> |
| + | </table> | ||
| + | == Function == | ||
| + | [[http://www.uniprot.org/uniprot/SPIKE_CVHSA SPIKE_CVHSA]] S1 attaches the virion to the cell membrane by interacting with human ACE2 and CLEC4M/DC-SIGNR, initiating the infection. Binding to the receptor and internalization of the virus into the endosomes of the host cell probably induces conformational changes in the S glycoprotein. Proteolysis by cathepsin CTSL may unmask the fusion peptide of S2 and activate membranes fusion within endosomes. S2 is 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. | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Cottrell, C A]] | ||
| + | [[Category: Kirchdoerfer, R N]] | ||
| + | [[Category: McLellan, J S]] | ||
| + | [[Category: Pallesen, J]] | ||
| + | [[Category: Turner, H L]] | ||
| + | [[Category: Wang, N]] | ||
| + | [[Category: Ward, A B]] | ||
| + | [[Category: Glycoprotein]] | ||
| + | [[Category: Membrane fusion]] | ||
| + | [[Category: Receptor binding]] | ||
| + | [[Category: Viral protein]] | ||
Revision as of 13:54, 11 April 2018
SARS Spike Glycoprotein, Trypsin-cleaved, Stabilized variant, C3 symmetry
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