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| | ==Crystal structure of the putative cap-binding domain of the PB2 subunit of Thogoto virus polymerase== | | ==Crystal structure of the putative cap-binding domain of the PB2 subunit of Thogoto virus polymerase== |
| - | <StructureSection load='4che' size='340' side='right' caption='[[4che]], [[Resolution|resolution]] 1.80Å' scene=''> | + | <StructureSection load='4che' size='340' side='right'caption='[[4che]], [[Resolution|resolution]] 1.80Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[4che]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Thogoto_virus Thogoto virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CHE OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4CHE FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[4che]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Thogoto_thogotovirus Thogoto thogotovirus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4CHE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4CHE FirstGlance]. <br> |
| - | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4cgs|4cgs]], [[4cgx|4cgx]], [[4chc|4chc]], [[4chd|4chd]], [[4chf|4chf]]</td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8Å</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=4che FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4che OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4che RCSB], [http://www.ebi.ac.uk/pdbsum/4che PDBsum]</span></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=4che FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4che OCA], [https://pdbe.org/4che PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4che RCSB], [https://www.ebi.ac.uk/pdbsum/4che PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4che ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/PB2_THOGV PB2_THOGV]] Initiates transcription by a unique cap-stealing mechanism that involves the cleavage of only the m(7)GpppAm structure from cellular hnRNAs. | + | [https://www.uniprot.org/uniprot/PB2_THOGV PB2_THOGV] Initiates transcription by a unique cap-stealing mechanism that involves the cleavage of only the m(7)GpppAm structure from cellular hnRNAs. |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> |
| | </div> | | </div> |
| | + | <div class="pdbe-citations 4che" style="background-color:#fffaf0;"></div> |
| | + | |
| | + | ==See Also== |
| | + | *[[RNA polymerase 3D structures|RNA polymerase 3D structures]] |
| | == References == | | == References == |
| | <references/> | | <references/> |
| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Thogoto virus]] | + | [[Category: Large Structures]] |
| - | [[Category: Bouvier, D]] | + | [[Category: Thogoto thogotovirus]] |
| - | [[Category: Crepin, T]] | + | [[Category: Bouvier D]] |
| - | [[Category: Cusack, S]] | + | [[Category: Crepin T]] |
| - | [[Category: Guilligay, D]] | + | [[Category: Cusack S]] |
| - | [[Category: Kadlec, J]] | + | [[Category: Guilligay D]] |
| - | [[Category: Kochs, G]] | + | [[Category: Kadlec J]] |
| - | [[Category: Lunardi, T]] | + | [[Category: Kochs G]] |
| - | [[Category: Ruigrok, R W.H]] | + | [[Category: Lunardi T]] |
| - | [[Category: Viral protein]]
| + | [[Category: Ruigrok RWH]] |
| Structural highlights
Function
PB2_THOGV Initiates transcription by a unique cap-stealing mechanism that involves the cleavage of only the m(7)GpppAm structure from cellular hnRNAs.
Publication Abstract from PubMed
Orthomyxovirus Influenza A virus (IAV) heterotrimeric polymerase performs transcription of viral mRNAs by cap-snatching, which involves generation of capped primers by host pre-mRNA binding via the PB2 subunit cap-binding site and cleavage 10-13 nucleotides from the 5' cap by the PA subunit endonuclease. Thogotoviruses, tick-borne orthomyxoviruses that includes Thogoto (THOV), Dhori (DHOV) and Jos (JOSV) viruses, are thought to perform cap-snatching by cleaving directly after the cap and thus have no heterogeneous, host-derived sequences at the 5' extremity of their mRNAs. Based on recent work identifying the cap-binding and endonuclease domains in IAV polymerase, we determined the crystal structures of two THOV PB2 domains, the putative cap-binding and the so-called '627-domain', and the structures of the putative endonuclease domains (PA-Nter) of THOV and DHOV. Despite low sequence similarity, corresponding domains have the same fold confirming the overall architectural similarity of orthomyxovirus polymerases. However the putative Thogotovirus cap-snatching domains in PA and PB2 have non-conservative substitutions of key active site residues. Biochemical analysis confirms that, unlike the IAV domains, the THOV and DHOV PA-Nter domains do not bind divalent cations and have no endonuclease activity and the THOV central PB2 domain does not bind cap analogues. On the other hand, sequence analysis suggests that other, non-influenza, orthomyxoviruses, such as salmon anemia virus (isavirus) and Quaranfil virus likely conserve active cap-snatching domains correlating with the reported occurrence of heterogeneous, host-derived sequences at the 5' end of the mRNAs of these viruses. These results highlight the unusual nature of transcription initiation by Thogotoviruses.
Comparative structural and functional analysis of orthomyxovirus polymerase cap-snatching domains.,Guilligay D, Kadlec J, Crepin T, Lunardi T, Bouvier D, Kochs G, Ruigrok RW, Cusack S PLoS One. 2014 Jan 15;9(1):e84973. doi: 10.1371/journal.pone.0084973. eCollection, 2014 Jan 15. PMID:24454773[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Guilligay D, Kadlec J, Crepin T, Lunardi T, Bouvier D, Kochs G, Ruigrok RW, Cusack S. Comparative structural and functional analysis of orthomyxovirus polymerase cap-snatching domains. PLoS One. 2014 Jan 15;9(1):e84973. doi: 10.1371/journal.pone.0084973. eCollection, 2014 Jan 15. PMID:24454773 doi:http://dx.doi.org/10.1371/journal.pone.0084973
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