X-ray Crystallographic Structure of the Norwalk Virus Capsid
- 8 October 1999
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 286 (5438), 287-290
- https://doi.org/10.1126/science.286.5438.287
Abstract
Norwalk virus, a noncultivatable human calicivirus, is the major cause of epidemic gastroenteritis in humans. The first x-ray structure of a calicivirus capsid, which consists of 180 copies of a single protein, has been determined by phase extension from a low-resolution electron microscopy structure. The capsid protein has a protruding (P) domain connected by a flexible hinge to a shell (S) domain that has a classical eight-stranded β-sandwich motif. The structure of the P domain is unlike that of any other viral protein with a subdomain exhibiting a fold similar to that of the second domain in the eukaryotic translation elongation factor–Tu. This subdomain, located at the exterior of the capsid, has the largest sequence variation among Norwalk-like human caliciviruses and is likely to contain the determinants of strain specificity and cell binding.Keywords
This publication has 30 references indexed in Scilit:
- Bivalent binding of a neutralising antibody to a calicivirus involves the torsional flexibility of the antibody hingeJournal of Molecular Biology, 1997
- Three-dimensional Structure of CalicivirusJournal of Molecular Biology, 1994
- The Refined Three-Dimensional Structure of an Insect Virus at 2·8 Å ResolutionJournal of Molecular Biology, 1994
- Protein Structure Comparison by Alignment of Distance MatricesJournal of Molecular Biology, 1993
- Structure and assembly of turnip crinkle virusJournal of Molecular Biology, 1986
- Structure and assembly of turnip crinkle virusJournal of Molecular Biology, 1986
- Subunit interactions in southern bean mosaic virusJournal of Molecular Biology, 1983
- Processing and post-refinement of oscillation camera dataJournal of Applied Crystallography, 1979
- Comparison of super-secondary structures in proteinsJournal of Molecular Biology, 1973
- The detection of sub-units within the crystallographic asymmetric unitActa Crystallographica, 1962