4aqf

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X-ray crystallographic structure of Crimean-congo haemorrhagic fever virus nucleoprotein

Structural highlights

4aqf is a 3 chain structure with sequence from Crimean-Congo hemorrhagic fever orthonairovirus. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 3.1Å
Ligands:SO4
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

NCAP_CCHFI

Publication Abstract from PubMed

Crimean-Congo haemorrhagic fever, a severe haemorrhagic disease found throughout Africa, Europe and Asia, is caused by the tick-borne Crimean-Congo haemorrhagic fever virus (CCHFV). CCHFV is a negative-sense single-stranded RNA virus belonging to the Nairovirus genus of the Bunyaviridae family. Its genome of three single-stranded RNA segments is encapsidated by the nucleocapsid protein (CCHFV N) to form the ribonucleoprotein complex. This ribonucleoprotein complex is required during replication and transcription of the viral genomic RNA. Here, we present the crystal structures of the CCHFV N in two distinct forms, an oligomeric form comprised of double antiparallel superhelices and a monomeric form. The head-to-tail interaction of the stalk region of one CCHFV N subunit with the base of the globular body of the adjacent subunit stabilises the helical organisation of the oligomeric form of CCHFV N. It also masks the conserved caspase-3 cleavage site present at the tip of the stalk region from host cell caspase-3 interaction and cleavage. By incubation with primer-length ssRNAs, we also obtained the crystal structure of CCHFV N in its monomeric form, which is similar to a recently published structure. The conformational change of CCHFV N upon de-oligomerisation results in the exposure of the caspase-3 cleavage site and subjects CCHFV N to caspase-3 cleavage. Mutations of this cleavage site inhibit cleavage by caspase-3 and result in enhanced viral polymerase activity. Thus, cleavage of CCHFV N by host cell caspase-3 appears to be crucial for controlling viral RNA synthesis and represents an important host defence mechanism against CCHFV infection.

STRUCTURE OF CRIMEAN-CONGO HAEMORRAGHIC FEVER VIRUS NUCLEOPROTEIN: SUPERHELICAL HOMO-OLIGOMERS AND THE ROLE OF CASPASE-3 CLEAVAGE.,Wang Y, Dutta S, Karlberg H, Devignot S, Weber F, Hao Q, Tan YJ, Mirazimi A, Kotaka M J Virol. 2012 Sep 5. PMID:22951837[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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See Also

References

  1. Wang Y, Dutta S, Karlberg H, Devignot S, Weber F, Hao Q, Tan YJ, Mirazimi A, Kotaka M. STRUCTURE OF CRIMEAN-CONGO HAEMORRAGHIC FEVER VIRUS NUCLEOPROTEIN: SUPERHELICAL HOMO-OLIGOMERS AND THE ROLE OF CASPASE-3 CLEAVAGE. J Virol. 2012 Sep 5. PMID:22951837 doi:http://dx.doi.org/10.1128/JVI.01627-12

Contents


PDB ID 4aqf

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