2ghv

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[[Image:2ghv.gif|left|200px]]
[[Image:2ghv.gif|left|200px]]
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{{Structure
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The line below this paragraph, containing "STRUCTURE_2ghv", creates the "Structure Box" on the page.
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|GENE= S ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id= Human SARS coronavirus])
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{{STRUCTURE_2ghv| PDB=2ghv | SCENE= }}
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|RELATEDENTRY=[[2ghw|2ghw]], [[2ajf|2ajf]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2ghv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2ghv OCA], [http://www.ebi.ac.uk/pdbsum/2ghv PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2ghv RCSB]</span>
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'''Crystal structure of SARS spike protein receptor binding domain'''
'''Crystal structure of SARS spike protein receptor binding domain'''
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[[Category: Stec, B.]]
[[Category: Stec, B.]]
[[Category: Sui, J.]]
[[Category: Sui, J.]]
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[[Category: s protein]]
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[[Category: S protein]]
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[[Category: sar]]
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[[Category: Sar]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 05:07:39 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 03:16:57 2008''
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Revision as of 02:07, 4 May 2008

Template:STRUCTURE 2ghv

Crystal structure of SARS spike protein receptor binding domain


Overview

Severe acute respiratory syndrome (SARS) is a newly emerged infectious disease that caused pandemic spread in 2003. The etiological agent of SARS is a novel coronavirus (SARS-CoV). The coronaviral surface spike protein S is a type I transmembrane glycoprotein that mediates initial host binding via the cell surface receptor angiotensin-converting enzyme 2 (ACE2), as well as the subsequent membrane fusion events required for cell entry. Here we report the crystal structure of the S1 receptor binding domain (RBD) in complex with a neutralizing antibody, 80R, at 2.3 A resolution, as well as the structure of the uncomplexed S1 RBD at 2.2 A resolution. We show that the 80R-binding epitope on the S1 RBD overlaps very closely with the ACE2-binding site, providing a rationale for the strong binding and broad neutralizing ability of the antibody. We provide a structural basis for the differential effects of certain mutations in the spike protein on 80R versus ACE2 binding, including escape mutants, which should facilitate the design of immunotherapeutics to treat a future SARS outbreak. We further show that the RBD of S1 forms dimers via an extensive interface that is disrupted in receptor- and antibody-bound crystal structures, and we propose a role for the dimer in virus stability and infectivity.

About this Structure

2GHV is a Single protein structure of sequence from Human sars coronavirus. Full crystallographic information is available from OCA.

Reference

Structural basis of neutralization by a human anti-severe acute respiratory syndrome spike protein antibody, 80R., Hwang WC, Lin Y, Santelli E, Sui J, Jaroszewski L, Stec B, Farzan M, Marasco WA, Liddington RC, J Biol Chem. 2006 Nov 10;281(45):34610-6. Epub 2006 Sep 5. PMID:16954221 Page seeded by OCA on Sun May 4 05:07:39 2008

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