2z0a: Difference between revisions
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==Crystal structure of RNA-binding domain of NS1 from influenza A virus A/crow/Kyoto/T1/2004(H5N1)== | |||
<StructureSection load='2z0a' size='340' side='right'caption='[[2z0a]], [[Resolution|resolution]] 1.85Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[2z0a]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Influenza_A_virus Influenza A virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2Z0A OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2Z0A 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]] 1.85Å</td></tr> | |||
== | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GLY:GLYCINE'>GLY</scene>, <scene name='pdbligand=SIN:SUCCINIC+ACID'>SIN</scene></td></tr> | ||
[[2z0a]] is a 4 chain structure | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2z0a FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2z0a OCA], [https://pdbe.org/2z0a PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2z0a RCSB], [https://www.ebi.ac.uk/pdbsum/2z0a PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2z0a ProSAT], [https://www.topsan.org/Proteins/RSGI/2z0a TOPSAN]</span></td></tr> | ||
</table> | |||
== Function == | |||
[https://www.uniprot.org/uniprot/Q5H7J4_9INFA Q5H7J4_9INFA] Inhibits post-transcriptional processing of cellular pre-mRNA, by binding and inhibiting two cellular proteins that are required for the 3'-end processing of cellular pre-mRNAs: the 30 kDa cleavage and polyadenylation specificity factor/CPSF4 and the poly(A)-binding protein 2/PABPN1. In turn, unprocessed 3' end pre-mRNAs accumulate in the host nucleus and are no longer exported to the cytoplasm. Cellular protein synthesis is thereby shut off very early after virus infection. Viral protein synthesis is not affected by the inhibition of the cellular 3' end processing machinery because the poly(A) tails of viral mRNAs are produced by the viral polymerase through a stuttering mechanism.[RuleBase:RU362113] Prevents the establishment of the cellular antiviral state by inhibiting TRIM25-mediated RIGI ubiquitination, which normally triggers the antiviral transduction signal that leads to the activation of type I IFN genes by transcription factors IRF3 and IRF7. Prevents human EIF2AK2/PKR activation, either by binding double-strand RNA, or by interacting directly with EIF2AK2/PKR. This function may be important at the very beginning of the infection, when NS1 is mainly present in the cytoplasm. Also binds poly(A) and U6 snRNA.[RuleBase:RU362113] | |||
==See Also== | ==See Also== | ||
*[[Nonstructural protein|Nonstructural protein]] | *[[Nonstructural protein 3D structures|Nonstructural protein 3D structures]] | ||
[[Category: Influenza | __TOC__ | ||
[[Category: Ito | </StructureSection> | ||
[[Category: Ito | [[Category: Influenza A virus]] | ||
[[Category: Kamo-Uchikubo | [[Category: Large Structures]] | ||
[[Category: Kishishita | [[Category: Ito H]] | ||
[[Category: Ito T]] | |||
[[Category: Saijo | [[Category: Kamo-Uchikubo T]] | ||
[[Category: Shirouzu | [[Category: Kishishita S]] | ||
[[Category: Terada | [[Category: Saijo S]] | ||
[[Category: Yokoyama | [[Category: Shirouzu M]] | ||
[[Category: Terada T]] | |||
[[Category: Yokoyama S]] | |||