2c86

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{{Structure
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2c86 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2c86 OCA], [http://www.ebi.ac.uk/pdbsum/2c86 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2c86 RCSB]</span>
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'''X-RAY STRUCTURE OF THE N AND C-TERMINAL DOMAIN OF CORONAVIRUS NUCLEOCAPSID PROTEIN.'''
'''X-RAY STRUCTURE OF THE N AND C-TERMINAL DOMAIN OF CORONAVIRUS NUCLEOCAPSID PROTEIN.'''
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[[Category: Ooi, A.]]
[[Category: Ooi, A.]]
[[Category: Prasad, B V.V.]]
[[Category: Prasad, B V.V.]]
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[[Category: nucleocapsid protein]]
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[[Category: Nucleocapsid protein]]
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[[Category: phosphorylation]]
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[[Category: Phosphorylation]]
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[[Category: rna-binding]]
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[[Category: Rna-binding]]
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[[Category: viral nucleoprotein]]
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[[Category: Viral nucleoprotein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 21:25:39 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 02:17:49 2008''
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Revision as of 18:25, 3 May 2008

Template:STRUCTURE 2c86

X-RAY STRUCTURE OF THE N AND C-TERMINAL DOMAIN OF CORONAVIRUS NUCLEOCAPSID PROTEIN.


Overview

Coronaviruses cause a variety of respiratory and enteric diseases in animals and humans including severe acute respiratory syndrome. In these enveloped viruses, the filamentous nucleocapsid is formed by the association of nucleocapsid (N) protein with single-stranded viral RNA. The N protein is a highly immunogenic phosphoprotein also implicated in viral genome replication and in modulating cell signaling pathways. We describe the structure of the two proteolytically resistant domains of the N protein from infectious bronchitis virus (IBV), a prototype coronavirus. These domains are located at its N- and C-terminal ends (NTD and CTD, respectively). The NTD of the IBV Gray strain at 1.3-A resolution exhibits a U-shaped structure, with two arms rich in basic residues, providing a module for specific interaction with RNA. The CTD forms a tightly intertwined dimer with an intermolecular four-stranded central beta-sheet platform flanked by alpha helices, indicating that the basic building block for coronavirus nucleocapsid formation is a dimeric assembly of N protein. The variety of quaternary arrangements of the NTD and CTD revealed by the analysis of the different crystal forms delineates possible interfaces that could be used for the formation of a flexible filamentous ribonucleocapsid. The striking similarity between the dimeric structure of CTD and the nucleocapsid-forming domain of a distantly related arterivirus indicates a conserved mechanism of nucleocapsid formation for these two viral families.

About this Structure

2C86 is a Single protein structure of sequence from Infectious bronchitis virus. Full crystallographic information is available from OCA.

Reference

X-ray structures of the N- and C-terminal domains of a coronavirus nucleocapsid protein: implications for nucleocapsid formation., Jayaram H, Fan H, Bowman BR, Ooi A, Jayaram J, Collisson EW, Lescar J, Prasad BV, J Virol. 2006 Jul;80(13):6612-20. PMID:16775348 Page seeded by OCA on Sat May 3 21:25:39 2008

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