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Molecules (Basel, Switzerland)|October 26, 2024
Mechanism-Based Allylic Carbasugar Chlorides That Form Covalent Intermediates with α- and β-GalactosidasesOluwafemi Akintola, Sandeep Bhosale, Andrew J BennetThe Journal of Organic Chemistry|January 30, 2020
Conformationally Controlled Reactivity of Carbasugars Uncovers the Choreography of Glycoside Hydrolase CatalysisPal John Pal Adabala, Saeideh Shamsi Kazem Abadi, Oluwafemi Akintola, et al.Bioorganic Chemistry|December 3, 2020
Structurally homologous sialidases exhibit a commonality in reactivity: Glycoside hydrolase-catalyzed hydrolysis of Kdn-thioglycosidesAli Nejatie, Oluwafemi Akintola, Elizabeth Steves, et al.Chemical Science|June 7, 2021
Glycoside hydrolase stabilization of transition state charge: new directions for inhibitor designWeiwu Ren, Marco Farren-Dai, Natalia Sannikova, et al.ACS Catalysis|October 10, 2024
Development of Tunable Mechanism-Based Carbasugar Ligands that Stabilize Glycoside Hydrolases through the Formation of Transient Covalent IntermediatesSandeep Bhosale, Sachin Kandalkar, Pierre-André Gilormini, et al.Nature Communications|August 15, 2018
Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic levelWeiwu Ren, Robert Pengelly, Marco Farren-Dai, et al.Nature Communications|September 9, 2018
Author Correction: Revealing the mechanism for covalent inhibition of glycoside hydrolases by carbasugars at an atomic levelWeiwu Ren, Robert Pengelly, Marco Farren-Dai, et al.Pageof 1