6t0w: Difference between revisions
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<StructureSection load='6t0w' size='340' side='right'caption='[[6t0w]], [[Resolution|resolution]] 3.18Å' scene=''> | <StructureSection load='6t0w' size='340' side='right'caption='[[6t0w]], [[Resolution|resolution]] 3.18Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6t0w]] is a 4 chain structure with sequence from [ | <table><tr><td colspan='2'>[[6t0w]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Influenza_B_virus Influenza B virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6T0W OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6T0W FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.18Å</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=6t0w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6t0w OCA], [https://pdbe.org/6t0w PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6t0w RCSB], [https://www.ebi.ac.uk/pdbsum/6t0w PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6t0w ProSAT]</span></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | |||
</table> | </table> | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/Q5V8Z9_9INFB Q5V8Z9_9INFB] | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</div> | </div> | ||
<div class="pdbe-citations 6t0w" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 6t0w" style="background-color:#fffaf0;"></div> | ||
==See Also== | |||
*[[RNA polymerase 3D structures|RNA polymerase 3D structures]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: Influenza B virus]] | |||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Cusack S]] | |||
[[Category: Cusack | [[Category: Karuppasamy M]] | ||
[[Category: Karuppasamy | [[Category: Kouba T]] | ||
[[Category: Kouba | [[Category: Wandzik JM]] | ||
[[Category: Wandzik | |||
Latest revision as of 13:17, 22 May 2024
Human Influenza B polymerase recycling complexHuman Influenza B polymerase recycling complex
Structural highlights
FunctionPublication Abstract from PubMedInfluenza polymerase uses unique mechanisms to synthesize capped and polyadenylated mRNAs from the genomic viral RNA (vRNA) template, which is packaged inside ribonucleoprotein particles (vRNPs). Here, we visualize by cryoelectron microscopy the conformational dynamics of the polymerase during the complete transcription cycle from pre-initiation to termination, focusing on the template trajectory. After exiting the active site cavity, the template 3' extremity rebinds into a specific site on the polymerase surface. Here, it remains sequestered during all subsequent transcription steps, forcing the template to loop out as it further translocates. At termination, the strained connection between the bound template 5' end and the active site results in polyadenylation by stuttering at uridine 17. Upon product dissociation, further conformational changes release the trapped template, allowing recycling back into the pre-initiation state. Influenza polymerase thus performs transcription while tightly binding to and protecting both template ends, allowing efficient production of multiple mRNAs from a single vRNP. A Structure-Based Model for the Complete Transcription Cycle of Influenza Polymerase.,Wandzik JM, Kouba T, Karuppasamy M, Pflug A, Drncova P, Provaznik J, Azevedo N, Cusack S Cell. 2020 Apr 16. pii: S0092-8674(20)30389-5. doi: 10.1016/j.cell.2020.03.061. PMID:32304664[1] From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See AlsoReferences
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