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Updated: Jun 27, 2026

Multi-target Parallel Processing Approach for Gene-to-structure Determination of the Influenza Polymerase PB2 Subunit
Published on: June 28, 2013
Sequence-structure relationships in polysaccharide co-polymerase (PCP) proteins
Renato Morona1, Leanne Purins, Ante Tocilj
1Australian Bacterial Pathogenesis Program, School of Molecular and Biomedical Science, Discipline of Microbiology and Immunology, University of Adelaide, North Terrace, Adelaide, SA 5005, Australia. renato.morona@adelaide.edu.au
Abstract:
Polysaccharides are ubiquitously distributed on the cell surface of bacteria. These polymers are involved in many processes, including immune avoidance and bacteria-host interactions, which are especially important for pathogenic organisms. In many instances, the lengths of these polysaccharides are not random, but rather distribute around some mean value, termed the modal length. A large family of proteins, called polysaccharide co-polymerases (PCPs), found in both Gram-negative and Gram-positive species regulate polysaccharide modal length. Recent crystal structures of Wzz proteins from Escherichia coli and Salmonella typhimurium provide the first atomic-resolution information for one family of PCPs, the PCP1 group. These crystal structures have important implications for the structures of other PCP families.
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