Ronald A Skurray, PhD

Affiliations: 
Genetics University of Sydney, Camperdown, New South Wales, Australia 
Area:
Plasmid biology, genetics of conjugation, F-plasmid genetics, drug resistance mechanisms in Gram negative and Gram positive bacteria
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"Ronald Skurray"
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Publications

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Chan HY, Jensen SO, LeBard RJ, et al. (2022) Molecular Analysis of pSK1 par: A Novel Plasmid Partitioning System Encoded by Staphylococcal Multiresistance Plasmids. Journal of Molecular Biology. 434: 167770
Firth N, Jensen SO, Kwong SM, et al. (2018) Staphylococcal Plasmids, Transposable and Integrative Elements. Microbiology Spectrum. 6
Brzoska AJ, Jensen SO, Barton DA, et al. (2016) Dynamic Filament Formation by a Divergent Bacterial Actin-Like ParM Protein. Plos One. 11: e0156944
Schumacher MA, Tonthat NK, Kwong SM, et al. (2014) Mechanism of staphylococcal multiresistance plasmid replication origin assembly by the RepA protein. Proceedings of the National Academy of Sciences of the United States of America. 111: 9121-6
Liu MA, Kwong SM, Pon CK, et al. (2012) Genetic requirements for replication initiation of the staphylococcal multiresistance plasmid pSK41. Microbiology (Reading, England). 158: 1456-67
Shearer JE, Wireman J, Hostetler J, et al. (2011) Major families of multiresistant plasmids from geographically and epidemiologically diverse staphylococci. G3 (Bethesda, Md.). 1: 581-91
Peters KM, Brooks BE, Schumacher MA, et al. (2011) A single acidic residue can guide binding site selection but does not govern QacR cationic-drug affinity. Plos One. 6: e15974
Jensen SO, Apisiridej S, Kwong SM, et al. (2010) Analysis of the prototypical Staphylococcus aureus multiresistance plasmid pSK1. Plasmid. 64: 135-42
Popp D, Xu W, Narita A, et al. (2010) Structure and filament dynamics of the pSK41 actin-like ParM protein: implications for plasmid DNA segregation. The Journal of Biological Chemistry. 285: 10130-40
Peters KM, Sharbeen G, Theis T, et al. (2009) Biochemical characterization of the multidrug regulator QacR distinguishes residues that are crucial to multidrug binding and induction of qacA transcription. Biochemistry. 48: 9794-800
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