7lv2

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Current revision (15:00, 6 March 2024) (edit) (undo)
 
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<StructureSection load='7lv2' size='340' side='right'caption='[[7lv2]], [[Resolution|resolution]] 1.30&Aring;' scene=''>
<StructureSection load='7lv2' size='340' side='right'caption='[[7lv2]], [[Resolution|resolution]] 1.30&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[7lv2]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7LV2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7LV2 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[7lv2]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Severe_acute_respiratory_syndrome_coronavirus_2 Severe acute respiratory syndrome coronavirus 2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7LV2 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7LV2 FirstGlance]. <br>
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</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=7lv2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7lv2 OCA], [https://pdbe.org/7lv2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7lv2 RCSB], [https://www.ebi.ac.uk/pdbsum/7lv2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7lv2 ProSAT]</span></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.301&#8491;</td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7lv2 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7lv2 OCA], [https://pdbe.org/7lv2 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7lv2 RCSB], [https://www.ebi.ac.uk/pdbsum/7lv2 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7lv2 ProSAT]</span></td></tr>
</table>
</table>
== Function ==
== Function ==
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[[https://www.uniprot.org/uniprot/NCAP_SARS2 NCAP_SARS2]] Packages the positive strand viral genome RNA into a helical ribonucleocapsid (RNP) and plays a fundamental role during virion assembly through its interactions with the viral genome and membrane protein M. Plays an important role in enhancing the efficiency of subgenomic viral RNA transcription as well as viral replication.
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[https://www.uniprot.org/uniprot/NCAP_SARS2 NCAP_SARS2] Packages the positive strand viral genome RNA into a helical ribonucleocapsid (RNP) and plays a fundamental role during virion assembly through its interactions with the viral genome and membrane protein M. Plays an important role in enhancing the efficiency of subgenomic viral RNA transcription as well as viral replication.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The SARS-CoV-2 Nucleoprotein (NCAP) functions in RNA packaging during viral replication and assembly. Computational analysis of its amino acid sequence reveals a central low-complexity domain (LCD) having sequence features akin to LCDs in other proteins known to function in liquid-liquid phase separation. Here we show that in the presence of viral RNA, NCAP, and also its LCD segment alone, form amyloid-like fibrils when undergoing liquid-liquid phase separation. Within the LCD we identified three 6-residue segments that drive amyloid fibril formation. We determined atomic structures for fibrils formed by each of the three identified segments. These structures informed our design of peptide inhibitors of NCAP fibril formation and liquid-liquid phase separation, suggesting a therapeutic route for Covid-19. One Sentence Summary: Atomic structures of amyloid-driving peptide segments from SARS-CoV-2 Nucleoprotein inform the development of Covid-19 therapeutics.
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Inhibition of amyloid formation of the Nucleoprotein of SARS-CoV-2.,Tayeb-Fligelman E, Cheng X, Tai C, Bowler JT, Griner S, Sawaya MR, Seidler PM, Jiang YX, Lu J, Rosenberg GM, Salwinski L, Abskharon R, Zee CT, Hou K, Li Y, Boyer DR, Murray KA, Falcon G, Anderson DH, Cascio D, Saelices L, Damoiseaux R, Guo F, Eisenberg DS bioRxiv. 2021 Mar 5. doi: 10.1101/2021.03.05.434000. PMID:33688654<ref>PMID:33688654</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 7lv2" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Cascio, D]]
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[[Category: Severe acute respiratory syndrome coronavirus 2]]
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[[Category: Eisenberg, D S]]
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[[Category: Cascio D]]
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[[Category: Hou, K]]
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[[Category: Eisenberg DS]]
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[[Category: Sawaya, M R]]
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[[Category: Hou K]]
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[[Category: Amyloid fibril]]
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[[Category: Sawaya MR]]
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[[Category: Protein fibril]]
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Current revision

GSQASS segment from the Nucleoprotein of SARS-CoV-2, residues 179-184

PDB ID 7lv2

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