3q7c | pdb_00003q7c

Exonuclease domain of Lassa virus nucleoprotein bound to manganese

spinqualitylabelsall models 3q7c, resolution 1.50Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 3q7c is a 1 chain structure with sequence from Lassa virus. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Ligands: MN, PO4, ZN Related: 3q7b Resources: FirstGlance, OCA, RCSB, PDBsum Publication Abstract from PubMed Lassa fever virus, a member of the family Arenaviridae, is a highly endemic category A pathogen that causes 300,000-500,000 infections per year in Western Africa. The arenaviral nucleoprotein NP has been implicated in suppression of the host innate immune system, but the mechanism by which this occurs has remained elusive. Here we present the crystal structure at 1.5 A of the immunosuppressive C-terminal portion of Lassa virus NP and illustrate that, unexpectedly, its 3D fold closely mimics that of the DEDDh family of exonucleases. Accompanying biochemical experiments illustrate that NP indeed has a previously unknown, bona fide exonuclease activity, with strict specificity for double-stranded RNA substrates. We further demonstrate that this exonuclease activity is essential for the ability of NP to suppress translocation of IFN regulatory factor 3 and block activation of the innate immune system. Thus, the nucleoprotein is a viral exonuclease with anti-immune activity, and this work provides a unique opportunity to combat arenaviral infections. Structure of the Lassa virus nucleoprotein reveals a dsRNA-specific 3' to 5' exonuclease activity essential for immune suppression.,Hastie KM, Kimberlin CR, Zandonatti MA, Macrae IJ, Saphire EO Proc Natl Acad Sci U S A. 2011 Jan 24. PMID:21262835 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine. See Also Nucleoprotein

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