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Expert Opinion on Drug Discovery|December 24, 2025
Protein crystallization strategies in structure-based drug designMargareta Ek, Linda Öster, Helena Käck, et al.Drug Discovery Today|May 21, 2018
Structural basis for selective inhibition of antibacterial target MraY, a membrane-bound enzyme involved in peptidoglycan synthesisJenny Hering, Elin Dunevall, Margareta Ek, et al.Proceedings of the National Academy of Sciences of the United States of America|February 23, 2013
Crystal structure of microsomal prostaglandin E2 synthase provides insight into diversity in the MAPEG superfamilyTove Sjögren, Johan Nord, Margareta Ek, et al.Nature Chemical Biology|January 10, 2017
MraY-antibiotic complex reveals details of tunicamycin mode of actionJonna K Hakulinen, Jenny Hering, Gisela Brändén, et al.Journal of Synchrotron Radiation|February 18, 2012
Solutions for the storage and handling of SPINE standard pucksCristian Bodin, Fredrik Mauritzson, Rob Horsefield, et al.ACS Chemical Biology|January 7, 2021
Branched Chain Lipid Metabolism As a Determinant of the N-Acyl Variation of Streptomyces Natural ProductsNeil P J Price, Michael A Jackson, Trina M Hartman, et al.Scientific Reports|October 1, 2020
The rapid "teabag" method for high-end purification of membrane proteinsJenny Hering, Julie Winkel Missel, Liying Zhang, et al.ACS Medicinal Chemistry Letters|April 22, 2022
Discovery by Virtual Screening of an Inhibitor of CDK5-Mediated PPARγ PhosphorylationGavin O'Mahony, Jens Petersen, Margareta Ek, et al.ACS Chemical Biology|November 9, 2020
Exploring the Active Site of the Antibacterial Target MraY by Modified TunicamycinsJenny Hering, Elin Dunevall, Arjan Snijder, et al.The Journal of Biological Chemistry|April 10, 2025
Mechanism and kinetics of turnover inhibitors of nicotinamide N-methyl transferase in vitro and in vivoTomas Akerud, Claudia De Fusco, Peter Brandt, et al.Pageof 2