| Literature DB >> 25528417 |
Sunil K Tewary1, Lingfei Liang1, Zihan Lin1, Annie Lynn1, Susan F Cotmore2, Peter Tattersall3, Haiyan Zhao4, Liang Tang5.
Abstract
Members of the Parvoviridae family all encode a non-structural protein 1 (NS1) that directs replication of single-stranded viral DNA, packages viral DNA into capsid, and serves as a potent transcriptional activator. Here we report the X-ray structure of the minute virus of mice (MVM) NS1 N-terminal domain at 1.45Å resolution, showing that sites for dsDNA binding, ssDNA binding and cleavage, nuclear localization, and other functions are integrated on a canonical fold of the histidine-hydrophobic-histidine superfamily of nucleases, including elements specific for this Protoparvovirus but distinct from its Bocaparvovirus or Dependoparvovirus orthologs. High resolution structural analysis reveals a nickase active site with an architecture that allows highly versatile metal ligand binding. The structures support a unified mechanism of replication origin recognition for homotelomeric and heterotelomeric parvoviruses, mediated by a basic-residue-rich hairpin and an adjacent helix in the initiator proteins and by tandem tetranucleotide motifs in the replication origins.Entities:
Keywords: DNA replication; Nickase; Non-structural protein 1; Nuclease; Parvovirus; Site-specific DNA binding
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Year: 2014 PMID: 25528417 PMCID: PMC4699654 DOI: 10.1016/j.virol.2014.11.022
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616