6mwn: Difference between revisions

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'''Unreleased structure'''


The entry 6mwn is ON HOLD  until Paper Publication
==Crystal structure of hepatitis A virus IRES domain V in complex with Fab HAVx==
<StructureSection load='6mwn' size='340' side='right'caption='[[6mwn]], [[Resolution|resolution]] 2.84&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6mwn]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Hepatovirus_A Hepatovirus A] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6MWN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6MWN FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.838&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GTP:GUANOSINE-5-TRIPHOSPHATE'>GTP</scene></td></tr>
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6mwn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6mwn OCA], [https://pdbe.org/6mwn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6mwn RCSB], [https://www.ebi.ac.uk/pdbsum/6mwn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6mwn ProSAT]</span></td></tr>
</table>
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Picornaviral IRES elements are essential for initiating the cap-independent viral translation. However, three-dimensional structures of these elements remain elusive. Here, we report a 2.84-A resolution crystal structure of hepatitis A virus IRES domain V (dV) in complex with a synthetic antibody fragment-a crystallization chaperone. The RNA adopts a three-way junction structure, topologically organized by an adenine-rich stem-loop motif. Despite no obvious sequence homology, the dV architecture shows a striking similarity to a circularly permuted form of encephalomyocarditis virus J-K domain, suggesting a conserved strategy for organizing the domain architecture. Recurrence of the motif led us to use homology modeling tools to compute a 3-dimensional structure of the corresponding domain of foot-and-mouth disease virus, revealing an analogous domain organizing motif. The topological conservation observed among these IRESs and other viral domains implicates a structured three-way junction as an architectural scaffold to pre-organize helical domains for recruiting the translation initiation machinery.


Authors: Koirala, D., Shao, Y., Piccirilli, J.A.
A conserved RNA structural motif for organizing topology within picornaviral internal ribosome entry sites.,Koirala D, Shao Y, Koldobskaya Y, Fuller JR, Watkins AM, Shelke SA, Pilipenko EV, Das R, Rice PA, Piccirilli JA Nat Commun. 2019 Aug 9;10(1):3629. doi: 10.1038/s41467-019-11585-z. PMID:31399592<ref>PMID:31399592</ref>


Description: Crystal structure of hepatitis A virus IRES domain V in complex with Fab HAVx
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
[[Category: Unreleased Structures]]
</div>
[[Category: Koirala, D]]
<div class="pdbe-citations 6mwn" style="background-color:#fffaf0;"></div>
[[Category: Shao, Y]]
 
[[Category: Piccirilli, J.A]]
==See Also==
*[[Antibody 3D structures|Antibody 3D structures]]
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Hepatovirus A]]
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Koirala D]]
[[Category: Piccirilli JA]]
[[Category: Shao Y]]

Latest revision as of 06:40, 11 October 2023

Crystal structure of hepatitis A virus IRES domain V in complex with Fab HAVx

6mwn, resolution 2.84Å

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