133 Publications (Page 1 of 6)
2021
Enzymatic Stetter Reaction: Computational Study of the Reaction Mechanism of MenD
ACS Catalysis. | Journal Article
2020
Structure-Based Drug Design of Bisubstrate Inhibitors of Phenylethanolamine N-Methyltransferase Possessing Low Nanomolar Affinity at Both Substrate Binding Domains1
Journal of Medicinal Chemistry. | Journal Article
2019
Computational characterization of enzyme-bound thiamin diphosphate reveals a surprisingly stable tricyclic state: implications for catalysisPlanas, Ferran⋅Mc Leish, Michael J and Himo, FahmiBeilstein Journal of Organic Chemistry, vol. 15, pp. 145–159.
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Computational Study of Enantioselective Carboligation Catalyzed by Benzoylformate DecarboxylasePlanas, Ferran⋅Mc Leish, Michael J. and Himo, FahmiACS Catalysis, pp. 5657–5667.
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2018
A Theoretical Study of the Benzoylformate Decarboxylase Reaction MechanismPlanas, Ferran⋅Sheng, Xiang⋅Mc Leish, Michael J and Himo, FahmiFrontiers in chemistry, vol. 6, pp. 205, 2018-00-00.
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2017
Environmental heterogeneity and the evolution of plant-virus interactions: Viruses in wild pepper populationsFraile, Aurora⋅Mc Leish, Michael J⋅Pagán, Israel⋅González-Jara, Pablo⋅Piñero, Daniel and García-Arenal, FernandoVirus Research, vol. 241, pp. 76, 2017-09-15.
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Phosphonodifluoropyruvate is a mechanism-based inhibitor of phosphonopyruvate decarboxylase from Bacteroides fragilis.
Bioorganic & medicinal chemistry. | Journal Article
Spatial correspondence between the specialist galling insect genus Kladothrips (Thysanoptera: Tubulifera: Phlaeothripidae) and its Acacia host: ecological and evolutionary constraints on host useMc Leish, Michael J⋅González‐Orozco, Carlos E and Miller, Joe TAustral Entomology, vol. 56, (no. 4), pp. 423, November 2017.
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Specificity and mechanism of mandelamide hydrolase catalysis.Adediran, S A⋅Wang, Pan-Fen⋅Shilabin, Abbas G⋅Baron, Charles A and Mc Leish, Michael JArchives of biochemistry and biophysics, January 24, 2017.
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Structure and mechanism of benzaldehyde dehydrogenase from Pseudomonas putida ATCC 12633, a member of the Class 3 aldehyde dehydrogenase superfamily.
Protein engineering, design & selection : PEDS. | Journal Article
2016
Mechanistic and Structural Insight to an Evolved Benzoylformate Decarboxylase with Enhanced Pyruvate Decarboxylase Activity
Catalysts. | Journal Article
2015
Crystal Structure of Benzoylformate Decarboxylase Mutant H281Y/T377P/F397T/A460IAndrews, F.H. and Mc Leish, M.J.Protein Data Bank, Rutgers University
The kinetic characterization and X-ray structure of a putative benzoylformate decarboxylase from M. smegmatis highlights the difficulties in the functional annotation of ThDP-dependent enzymesAndrews, F.H.⋅Horton, J.D.⋅Shin, D.⋅Yoon, H.-J.⋅Logsdon, M.G.⋅Malik, A.M.⋅Rogers, M.P.⋅Kneen, M.M.⋅Suh, S.W. and Mc Leish, M.J.Biochimica et Biophysica Acta - Proteins and Proteomics, vol. 1854, pp. 1001-1009.
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2014
Crystal Structure of Benzoylformate Decarboxylase Mutant A306FAndrews, F.H. and Mc Leish, M.J.Protein Data Bank, Rutgers University
Extended reaction scope of thiamine diphosphate dependent cyclohexane-1,2-dione hydrolase: From C-C bond cleavage to C-C bond ligationLoschonsky, S.⋅Wacker, T.⋅Waltzer, S.⋅Giovannini, P.P.⋅Mc Leish, M.J.⋅Andrade, S.L.A. and Müller, M.Angewandte Chemie - International Edition, vol. 53, pp. 14402-14406.
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Identification of charge transfer transitions related to thiamin-bound intermediates on enzymes provides a plethora of signatures useful in mechanistic studies.Patel, Hetalben⋅Nemeria, Natalia S⋅Andrews, Forest H⋅Mc Leish, Michael J and Jordan, FrankBiochemistry, vol. 53, (no. 13), pp. 2145-52, 2014/Apr/8.
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Perturbation of the monomer-monomer interfaces of the benzoylformate decarboxylase tetramerAndrews, F.H.⋅Rogers, M.P.⋅Paul, L.N. and Mc Leish, M.J.Biochemistry, vol. 53, pp. 4358-4367.
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2013
A bulky hydrophobic residue is not required to maintain the V-conformation of enzyme-bound thiamin diphosphate.Andrews, Forest H⋅Andrews, F.H.⋅Tom, Alan R⋅Tom, A.R.⋅Gunderman, P.R.⋅Gunderman, Peter R⋅Novak, W.R.P.⋅Novak, Walter R⋅Mc Leish, Michael J and McLeish, M.J.Biochemistry, vol. 52, (no. 18), pp. 3028-30, 2013/May/7.
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Kinetic and pH studies on human phenylethanolamine N-methyltransferaseWu, Q. and Mc Leish, M.J.Archives of Biochemistry and Biophysics, vol. 539, pp. 1-8.
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Using site-saturation mutagenesis to explore mechanism and substrate specificity in thiamin diphosphate-dependent enzymes.Andrews, Forest H and Mc Leish, Michael JThe FEBS journal, vol. 280, (no. 24), pp. 6395-6411, December 2013.
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2012
Substrate specificity in thiamin diphosphate-dependent decarboxylases.Andrews, Forest H and Mc Leish, Michael JBioorganic chemistry, vol. 43, pp. 26-36, 2012/Aug.
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2011
Characterization of a thiamin diphosphate-dependent phenylpyruvate decarboxylase from SaccharomycescerevisiaeKneen, Malea M⋅Stan, Razvan⋅Yep, Alejandra⋅Tyler, Ryan P⋅Saehuan, Choedchai and Mc Leish, Michael JThe FEBS Journal, vol. 278, (no. 11), pp. 1842-1853, Jun 2011.
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Characterization of a thiamin diphosphate-dependent phenylpyruvate decarboxylase from Saccharomyces cerevisiae.Kneen, Malea M⋅Stan, Razvan⋅Yep, Alejandra⋅Tyler, Ryan P⋅Saehuan, Choedchai and Mc Leish, Michael JThe FEBS journal, vol. 278, (no. 11), pp. 1842-53, 2011/Jun.
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2010
Active-site engineering of benzaldehyde lyase shows that a point mutation can confer both new reactivity and susceptibility to mechanism-based inhibition.Brandt, Gabriel S⋅Kneen, Malea M⋅Petsko, Greg⋅Ringe, Dagmar and Mc Leish, Michael JJournal of the American Chemical Society, vol. 132, (no. 2), pp. 438-9, 2010/Jan/20.
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Fragment-based screening by X-ray crystallography, MS and isothermal titration calorimetry to identify PNMT (phenylethanolamine N-methyltransferase) inhibitors.Drinkwater, Nyssa⋅Drinkwater, Nyssa⋅Vu, Hoan⋅Vu, Hoan⋅Lovell, Kimberly M⋅Lovell, Kimberly M.⋅Criscione, Kevin R⋅Criscione, Kevin R.⋅Collins, Brett M.⋅Collins, Brett M⋅Prisinzano, Thomas E⋅Prisinzano, Thomas E.⋅Poulsen, Sally-Ann⋅Poulsen, Sally-Ann⋅Mc Leish, Michael J⋅McLeish, Michael J.⋅Grunewald, Gary L.⋅Grunewald, Gary L⋅Martin, Jennifer L. and Martin, Jennifer LThe Biochemical journal, vol. 431, (no. 1), pp. 51-61, 2010/Oct/1.
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