6crx: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
m Protected "6crx" [edit=sysop:move=sysop]
OCA (talk | contribs)
No edit summary
Line 1: Line 1:
'''Unreleased structure'''


The entry 6crx is ON HOLD
==SARS Spike Glycoprotein, Stabilized variant, two S1 CTDs in the upwards conformation==
 
<StructureSection load='6crx' size='340' side='right' caption='[[6crx]], [[Resolution|resolution]] 3.90&Aring;' scene=''>
Authors: Kirchdoerfer, R.N., Wang, N., Pallesen, J., Turner, H.L., Cottrell, C.A., McLellan, J.S., Ward, A.B.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[6crx]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6CRX OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6CRX FirstGlance]. <br>
Description: SARS Spike Glycoprotein, Stabilized variant, two S1 CTDs in the upwards conformation
</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: Unreleased Structures]]
<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=6crx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6crx OCA], [http://pdbe.org/6crx PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6crx RCSB], [http://www.ebi.ac.uk/pdbsum/6crx PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6crx 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: Pallesen, J]]
[[Category: Ward, A.B]]
[[Category: Turner, H L]]
[[Category: Cottrell, C.A]]
[[Category: Mclellan, J.S]]
[[Category: Kirchdoerfer, R.N]]
[[Category: Turner, H.L]]
[[Category: Wang, N]]
[[Category: Wang, N]]
[[Category: Ward, A B]]
[[Category: Glycoprotein]]
[[Category: Membrane fusion]]
[[Category: Receptor binding]]
[[Category: Viral protein]]