9shv: Difference between revisions

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'''Unreleased structure'''


The entry 9shv is ON HOLD  until Paper Publication
==Prefusion-stabilized Hendra virus fusion protein in complex with inhibitory nanobody F123==
 
<StructureSection load='9shv' size='340' side='right'caption='[[9shv]], [[Resolution|resolution]] 2.87&Aring;' scene=''>
Authors: Kralova, A., Hanke, L.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9shv]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Henipavirus_hendraense Henipavirus hendraense] and [https://en.wikipedia.org/wiki/Vicugna_pacos Vicugna pacos]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9SHV OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9SHV FirstGlance]. <br>
Description: Prefusion-stabilized Hendra virus fusion protein in complex with inhibitory nanobody F123
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.87&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9shv FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9shv OCA], [https://pdbe.org/9shv PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9shv RCSB], [https://www.ebi.ac.uk/pdbsum/9shv PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9shv ProSAT]</span></td></tr>
[[Category: Hanke, L]]
</table>
[[Category: Kralova, A]]
== Function ==
[https://www.uniprot.org/uniprot/FUS_HENDH FUS_HENDH] Class I viral fusion protein. Under the current model, the protein has at least 3 conformational states: pre-fusion native state, pre-hairpin intermediate state, and post-fusion hairpin state. During viral and plasma cell membrane fusion, the heptad repeat (HR) regions 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 plasma cell membranes. Directs fusion of viral and cellular membranes leading to delivery of the nucleocapsid into the cytoplasm. This fusion is pH independent and occurs directly at the outer cell membrane. The trimer of F1-F2 (F protein) probably interacts with HN at the virion surface. Upon HN binding to its cellular receptor, the hydrophobic fusion peptide is unmasked and interacts with the cellular membrane, inducing the fusion between cell and virion membranes. Later in infection, F proteins expressed at the plasma membrane of infected cells could mediate fusion with adjacent cells to form syncytia, a cytopathic effect that could lead to tissue necrosis (By similarity).
__TOC__
</StructureSection>
[[Category: Henipavirus hendraense]]
[[Category: Large Structures]]
[[Category: Vicugna pacos]]
[[Category: Hanke L]]
[[Category: Kralova A]]

Latest revision as of 08:04, 9 September 2026

Prefusion-stabilized Hendra virus fusion protein in complex with inhibitory nanobody F123

9shv, resolution 2.87Å

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