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Sherine E Thomas

Showing results (11-20 of 18) with videos related to

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Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|April 30, 2019
Structure-guided fragment-based drug discovery at the synchrotron: screening binding sites and correlations with hotspot mappingSherine E Thomas, Patrick Collins, Rory Hennell James, et al.
Frontiers in Molecular Biosciences|June 17, 2022
Structural Characterization of <i>Mycobacterium abscessus</i> Phosphopantetheine Adenylyl Transferase Ligand Interactions: Implications for Fragment-Based Drug DesignSherine E Thomas, William J McCarthy, Jamal El Bakali, et al.
Computational and Structural Biotechnology Journal|July 8, 2021
Predicted structural mimicry of spike receptor-binding motifs from highly pathogenic human coronavirusesChristopher A Beaudoin, Arian R Jamasb, Ali F Alsulami, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2018
Arginine-deprivation-induced oxidative damage sterilizes <i>Mycobacterium tuberculosis</i>Sangeeta Tiwari, Andries J van Tonder, Catherine Vilchèze, et al.
Journal of Medicinal Chemistry|July 9, 2019
Development of Inhibitors against <i>Mycobacterium abscessus</i> tRNA (m<sup>1</sup>G37) Methyltransferase (TrmD) Using Fragment-Based ApproachesAndrew J Whitehouse, Sherine E Thomas, Karen P Brown, et al.
Computational and Structural Biotechnology Journal|July 1, 2021
A fragment-based approach to assess the ligandability of ArgB, ArgC, ArgD and ArgF in the L-arginine biosynthetic pathway of <i>Mycobacterium tuberculosis</i>Pooja Gupta, Sherine E Thomas, Shaymaa A Zaidan, et al.
ACS Infectious Diseases|January 17, 2022
Development of Inhibitors of SAICAR Synthetase (PurC) from <i>Mycobacterium abscessus</i> Using a Fragment-Based ApproachSitthivut Charoensutthivarakul, Sherine E Thomas, Amy Curran, et al.
Nucleic Acids Research|July 1, 2020
Fragment-based discovery of a new class of inhibitors targeting mycobacterial tRNA modificationSherine E Thomas, Andrew J Whitehouse, Karen Brown, et al.
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Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Philosophical Transactions. Series A, Mathematical, Physical, and Engineering Sciences|April 30, 2019
Structure-guided fragment-based drug discovery at the synchrotron: screening binding sites and correlations with hotspot mappingSherine E Thomas, Patrick Collins, Rory Hennell James, et al.
Frontiers in Molecular Biosciences|June 17, 2022
Structural Characterization of <i>Mycobacterium abscessus</i> Phosphopantetheine Adenylyl Transferase Ligand Interactions: Implications for Fragment-Based Drug DesignSherine E Thomas, William J McCarthy, Jamal El Bakali, et al.
Computational and Structural Biotechnology Journal|July 8, 2021
Predicted structural mimicry of spike receptor-binding motifs from highly pathogenic human coronavirusesChristopher A Beaudoin, Arian R Jamasb, Ali F Alsulami, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 2018
Arginine-deprivation-induced oxidative damage sterilizes <i>Mycobacterium tuberculosis</i>Sangeeta Tiwari, Andries J van Tonder, Catherine Vilchèze, et al.
Journal of Medicinal Chemistry|July 9, 2019
Development of Inhibitors against <i>Mycobacterium abscessus</i> tRNA (m<sup>1</sup>G37) Methyltransferase (TrmD) Using Fragment-Based ApproachesAndrew J Whitehouse, Sherine E Thomas, Karen P Brown, et al.
Computational and Structural Biotechnology Journal|July 1, 2021
A fragment-based approach to assess the ligandability of ArgB, ArgC, ArgD and ArgF in the L-arginine biosynthetic pathway of <i>Mycobacterium tuberculosis</i>Pooja Gupta, Sherine E Thomas, Shaymaa A Zaidan, et al.
ACS Infectious Diseases|January 17, 2022
Development of Inhibitors of SAICAR Synthetase (PurC) from <i>Mycobacterium abscessus</i> Using a Fragment-Based ApproachSitthivut Charoensutthivarakul, Sherine E Thomas, Amy Curran, et al.
Nucleic Acids Research|July 1, 2020
Fragment-based discovery of a new class of inhibitors targeting mycobacterial tRNA modificationSherine E Thomas, Andrew J Whitehouse, Karen Brown, et al.
Pageof 2