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Bioorganic & Medicinal Chemistry Letters|February 14, 2019
Design, synthesis and evaluation of a series of 5-methoxy-2,3-naphthalimide derivatives as AcrB inhibitors for the reversal of bacterial resistanceChaobin Jin, Rawaf Alenazy, Yinhu Wang, et al.
Current Topics in Medicinal Chemistry|November 19, 2013
Structure guided design of biotin protein ligase inhibitors for antibiotic discoveryAshleigh S Paparella, Tatiana P Soares da Costa, Min Y Yap, et al.
The International Journal of Biochemistry & Cell Biology|July 31, 2007
Conserved Glu40 and Glu433 of the biotin carboxylase domain of yeast pyruvate carboxylase I isoenzyme are essential for the association of tetramersSarawut Jitrapakdee, Katharina H Surinya, Abdussalam Adina-Zada, et al.
Molecular Microbiology|November 23, 2013
Dual roles of F123 in protein homodimerization and inhibitor binding to biotin protein ligase from Staphylococcus aureusTatiana P Soares da Costa, Min Y Yap, Matthew A Perugini, et al.
Bioorganic & Medicinal Chemistry Letters|September 7, 2014
Heterocyclic acyl-phosphate bioisostere-based inhibitors of Staphylococcus aureus biotin protein ligaseWilliam Tieu, Angie M Jarrad, Ashleigh S Paparella, et al.
Archives of Biochemistry and Biophysics|July 28, 2020
Biochemical characterisation of class III biotin protein ligases from Botrytis cinerea and Zymoseptoria triticiLouise M Sternicki, Stephanie Nguyen, Kamila J Pacholarz, et al.
Frontiers in Microbiology|September 15, 2022
Cinnamaldehyde derivatives act as antimicrobial agents against <i>Acinetobacter baumannii</i> through the inhibition of cell divisionWern Chern Chai, Jonathan J Whittall, Steven W Polyak, et al.
ACS Infectious Diseases|November 14, 2017
Halogenation of Biotin Protein Ligase Inhibitors Improves Whole Cell Activity against Staphylococcus aureusAshleigh S Paparella, Kwang Jun Lee, Andrew J Hayes, et al.
Protein Science : a Publication of the Protein Society|April 6, 2013
Structural characterization of Staphylococcus aureus biotin protein ligase and interaction partners: an antibiotic targetNicole R Pendini, Min Y Yap, D A K Traore, et al.
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