Nigel G. J. Richards

University of Florida, Gainesville, Gainesville, FL, United States 
 2015 Purdue University, West Lafayette, IN, United States 
 2015- Cardiff University, Cardiff, Wales, United Kingdom 
Physical Chemistry, Biochemistry
"Nigel Gordon John Richards"

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Jin Y, Richards NG, Waltho JP, et al. (2017) Metal Fluorides as Analogues for Studies on Phosphoryl Transfer Enzymes. Angewandte Chemie (International Ed. in English). 56: 4110-4128
Kumar A, Khan A, Malhotra S, et al. (2016) Synthesis of macromolecular systems via lipase catalyzed biocatalytic reactions: applications and future perspectives. Chemical Society Reviews. 45: 6855-6887
Zhu W, Easthon LM, Reinhardt LA, et al. (2016) Substrate Binding Mode and Molecular Basis of a Specificity Switch in Oxalate Decarboxylase. Biochemistry. 55: 2163-73
Jin Y, Molt RW, Waltho JP, et al. (2016) (19)F NMR and DFT Analysis Reveal Structural and Electronic Transition State Features for RhoA-Catalyzed GTP Hydrolysis. Angewandte Chemie (International Ed. in English). 55: 3318-22
Zhu W, Wilcoxen J, Britt RD, et al. (2016) Formation of Hexacoordinate Mn(III) in Bacillus subtilis Oxalate Decarboxylase Requires Catalytic Turnover. Biochemistry. 55: 429-34
Vladimirova A, Patskovsky Y, Fedorov AA, et al. (2016) Substrate Distortion and the Catalytic Reaction Mechanism of 5-Carboxyvanillate Decarboxylase. Journal of the American Chemical Society. 138: 826-36
Georgiadis MM, Singh I, Kellett WF, et al. (2015) Structural basis for a six nucleotide genetic alphabet. Journal of the American Chemical Society. 137: 6947-55
Molt RW, Lecher AM, Clark T, et al. (2015) Facile C(sp(2))-C(sp(2)) bond cleavage in oxalic acid-derived radicals. Journal of the American Chemical Society. 137: 3248-52
Twahir UT, Stedwell CN, Lee CT, et al. (2015) Observation of superoxide production during catalysis of Bacillus subtilis oxalate decarboxylase at pH 4. Free Radical Biology & Medicine. 80: 59-66
Miao J, Richards NG, Ge H. (2014) Rhodium-catalyzed direct synthesis of unprotected NH-sulfoximines from sulfoxides. Chemical Communications (Cambridge, England). 50: 9687-9
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