Michael L. Sinnott

Affiliations: 
1987 University of Bristol, Bristol, England, United Kingdom 
 1987-1996 University of Illinois at Chicago, Chicago, IL, United States 
 1996-2003 Institute of Science and Technology The University of Manchester, Manchester, England, United Kingdom 
 2003- University of Huddersfield 
Area:
Organic chemistry
Website:
https://www.hud.ac.uk/ourstaff/profile/index.php?staffuid=sappmls
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"Michael L. Sinnott"
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DOI: 10.1021/jo01263a095

Mean distance: 19.36
 
SNBCP
Cross-listing: Chemistry Tree

Parents

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Mark C. Whiting grad student 1968 University of Bristol (Chemistry Tree)

Children

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Andrew Bennet grad student University of Huddersfield (Chemistry Tree)
Stephen G. Withers grad student 1977 University of Bristol (Chemistry Tree)
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Publications

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Neustroev KN, Golubev AM, Sinnott ML, et al. (2006) Transferase and hydrolytic activities of the laminarinase from Rhodothermus marinus and its M133A, M133C, and M133W mutants. Glycoconjugate Journal. 23: 501-11
Hart DO, He S, Chany CJ, et al. (2000) Identification of Asp-130 as the catalytic nucleophile in the main alpha-galactosidase from Phanerochaete chrysosporium, a family 27 glycosyl hydrolase. Biochemistry. 39: 9826-36
Andrews SR, Charnock SJ, Lakey JH, et al. (2000) Substrate specificity in glycoside hydrolase family 10. Tyrosine 87 and leucine 314 play a pivotal role in discriminating between glucose and xylose binding in the proximal active site of Pseudomonas cellulosa xylanase 10A. The Journal of Biological Chemistry. 275: 23027-33
Becker D, Johnson KS, Koivula A, et al. (2000) Hydrolyses of alpha- and beta-cellobiosyl fluorides by Cel6A (cellobiohydrolase II) of Trichoderma reesei and Humicola insolens. The Biochemical Journal. 345: 315-9
Brumer H, Sims PF, Sinnott ML. (1999) Lignocellulose degradation by Phanerochaete chrysosporium: purification and characterization of the main alpha-galactosidase. The Biochemical Journal. 339: 43-53
Zhao Y, Chany CJ, Sims PF, et al. (1997) Definition of the substrate specificity of the 'sensing' xylanase of Streptomyces cyaneus using xylooligosaccharide and cellooligosaccharide glycosides of 3,4-dinitrophenol. Journal of Biotechnology. 57: 181-90
Calugaru SV, Krishnan S, Chany CJ, et al. (1997) Larger increases in sensitivity to paracatalytic inactivation than in catalytic competence during experimental evolution of the second beta-galactosidase of Escherichia coli. The Biochemical Journal. 325: 117-21
Krishnan S, Hall BG, Sinnott ML. (1995) Catalytic consequences of experimental evolution: catalysis by a 'third-generation' evolvant of the second beta-galactosidase of Escherichia coli, ebgabcde, and by ebgabcd, a 'second-generation' evolvant containing two supposedly 'kinetically silent' mutations. The Biochemical Journal. 312: 971-7
Calugaru SV, Hall BG, Sinnott ML. (1995) Catalysis by the large subunit of the second beta-galactosidase of Escherichia coli in the absence of the small subunit. The Biochemical Journal. 312: 281-6
Guo X, Sinnott ML. (1993) A kinetic-isotope-effect study of catalysis by Vibrio cholerae neuraminidase. The Biochemical Journal. 294: 653-6
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