5wtf: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
No edit summary
No edit summary
Line 1: Line 1:


==Cryo-EM structure for Hepatitis A virus empty particle==
==Cryo-EM structure for Hepatitis A virus empty particle==
<StructureSection load='5wtf' size='340' side='right' caption='[[5wtf]], [[Resolution|resolution]] 3.90&Aring;' scene=''>
<StructureSection load='5wtf' size='340' side='right'caption='[[5wtf]], [[Resolution|resolution]] 3.90&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
<table><tr><td colspan='2'>[[5wtf]] is a 3 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5WTF OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5WTF FirstGlance]. <br>
<table><tr><td colspan='2'>[[5wtf]] is a 3 chain structure with sequence from [http://en.wikipedia.org/wiki/Hav Hav]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5WTF OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5WTF FirstGlance]. <br>
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5wte|5wte]], [[5wth|5wth]]</td></tr>
</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5wte|5wte]], [[5wth|5wth]]</td></tr>
<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=5wtf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5wtf OCA], [http://pdbe.org/5wtf PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5wtf RCSB], [http://www.ebi.ac.uk/pdbsum/5wtf PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5wtf ProSAT]</span></td></tr>
<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=5wtf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5wtf OCA], [http://pdbe.org/5wtf PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5wtf RCSB], [http://www.ebi.ac.uk/pdbsum/5wtf PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5wtf ProSAT]</span></td></tr>
Line 20: Line 20:
__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Hav]]
[[Category: Large Structures]]
[[Category: Dang, M]]
[[Category: Dang, M]]
[[Category: Fry, E E]]
[[Category: Fry, E E]]
Line 34: Line 36:
[[Category: Zhang, B]]
[[Category: Zhang, B]]
[[Category: Zhu, L]]
[[Category: Zhu, L]]
[[Category: Hav]]
[[Category: Neutralizing mechanism]]
[[Category: Neutralizing mechanism]]
[[Category: Receptor recognition]]
[[Category: Receptor recognition]]
[[Category: Viral entry]]
[[Category: Viral entry]]
[[Category: Virus]]
[[Category: Virus]]

Revision as of 10:26, 6 November 2019

Cryo-EM structure for Hepatitis A virus empty particleCryo-EM structure for Hepatitis A virus empty particle

Structural highlights

5wtf is a 3 chain structure with sequence from Hav. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Publication Abstract from PubMed

Hepatitis A virus (HAV) infects approximately 1.4 million people annually and, although there is a vaccine, there are no licensed therapeutic drugs. HAV is unusually stable (making disinfection problematic) and little is known of how it enters cells and releases its RNA. Here we report a potent HAV-specific monoclonal antibody, R10, which neutralizes HAV infection by blocking attachment to the host cell. High-resolution cryo-EM structures of HAV full and empty particles and of the complex of HAV with R10 Fab reveal the atomic details of antibody binding and point to a receptor recognition site at the pentamer interface. These results, together with our observation that the R10 Fab destabilizes the capsid, suggest the use of a receptor mimic mechanism to neutralize virus infection, providing new opportunities for therapeutic intervention.

Potent neutralization of hepatitis A virus reveals a receptor mimic mechanism and the receptor recognition site.,Wang X, Zhu L, Dang M, Hu Z, Gao Q, Yuan S, Sun Y, Zhang B, Ren J, Kotecha A, Walter TS, Wang J, Fry EE, Stuart DI, Rao Z Proc Natl Acad Sci U S A. 2017 Jan 10. pii: 201616502. doi:, 10.1073/pnas.1616502114. PMID:28074040[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

  1. Wang X, Zhu L, Dang M, Hu Z, Gao Q, Yuan S, Sun Y, Zhang B, Ren J, Kotecha A, Walter TS, Wang J, Fry EE, Stuart DI, Rao Z. Potent neutralization of hepatitis A virus reveals a receptor mimic mechanism and the receptor recognition site. Proc Natl Acad Sci U S A. 2017 Jan 10. pii: 201616502. doi:, 10.1073/pnas.1616502114. PMID:28074040 doi:http://dx.doi.org/10.1073/pnas.1616502114

5wtf, resolution 3.90Å

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA