Rohan Williams
Affiliations: | 2013- | University of Toronto, Toronto, ON, Canada |
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"Rohan Williams"Mean distance: 9.17 | S | N | B | C | P |
Parents
Sign in to add mentor| Spencer John Williams | grad student | 2010-2013 | University of Melbourne |
| Mark Nitz | post-doc | 2013- | University of Toronto |
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Publications
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| Marmont LS, Whitfield GB, Pfoh R, et al. (2020) PelX is a UDP-N-acetylglucosamine C4-epimerase involved in Pel polysaccharide-dependent biofilm formation. The Journal of Biological Chemistry |
| Abbott W, Alber O, Bayer E, et al. (2018) Ten years of CAZypedia: a living encyclopedia of carbohydrate-active enzymes Glycobiology. 28: 3-8 |
| Brown AC, Bryant JM, Einer-Jensen K, et al. (2015) Rapid Whole-Genome Sequencing of Mycobacterium tuberculosis Isolates Directly from Clinical Samples. Journal of Clinical Microbiology. 53: 2230-7 |
| Tankrathok A, Iglesias-Fernández J, Williams RJ, et al. (2015) A Single Glycosidase Harnesses Different Pyranoside Ring Transition State Conformations for Hydrolysis of Mannosides and Glucosides Acs Catalysis. 5: 6041-6051 |
| Williams RJ, Paul CE, Nitz M. (2014) Protecting-group-free O-glysosidation using p-toluenesulfonohydrazide and glycosyl chloride donors. Carbohydrate Research. 386: 73-7 |
| Williams RJ, Iglesias-Fernández J, Stepper J, et al. (2014) Combined inhibitor free-energy landscape and structural analysis reports on the mannosidase conformational coordinate. Angewandte Chemie (International Ed. in English). 53: 1087-91 |
| Tsegay S, Williams RJ, Williams SJ. (2012) Synthesis of glycosyl fluorides from thio-, seleno-, and telluroglycosides and glycosyl sulfoxides using aminodifluorosulfinium tetrafluoroborates. Carbohydrate Research. 357: 16-22 |
| Thompson AJ, Williams RJ, Hakki Z, et al. (2012) Structural and mechanistic insight into N-glycan processing by endo-α-mannosidase. Proceedings of the National Academy of Sciences of the United States of America. 109: 781-6 |
| Williams RJ, McGill NW, White JM, et al. (2010) Neighboring group participation in glycosylation reactions by 2,6-disubstituted 2-O-benzoyl groups: A mechanistic investigation Journal of Carbohydrate Chemistry. 29: 236-263 |