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    J Virol. 2005 Aug;79(16):10268-77.

    Structure of the Flavivirus helicase: implications for catalytic activity, protein interactions, and proteolytic processing.

    Wu J, Bera AK, Kuhn RJ, Smith JL.

    Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907, USA.

    Yellow fever virus (YFV), a member of the Flavivirus genus, has a plus-sense RNA genome encoding a single polyprotein. Viral protein NS3 includes a protease and a helicase that are essential to virus replication and to RNA capping. The 1.8-A crystal structure of the helicase region of the YFV NS3 protein includes residues 187 to 623. Two familiar helicase domains bind nucleotide in a triphosphate pocket without base recognition, providing a site for nonspecific hydrolysis of nucleoside triphosphates and RNA triphosphate. The third, C-terminal domain has a unique structure and is proposed to function in RNA and protein recognition. The organization of the three domains indicates that cleavage of the viral polyprotein NS3-NS4A junction occurs in trans.

    PMID: 16051820 [PubMed - indexed for MEDLINE]

    PMCID: 1182653

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