Johannes Schiebel

Rational optimization of drug-target residence time: insights from inhibitor binding to the Staphylococcus aureus FabI enzyme-product complex.

Peter J. Tonge, Christoph A. Sotriffer, Weixuan Yu, 2013, Biochemistry.

Structures of endothiapepsin-fragment complexes from crystallographic fragment screening using a novel, diverse and affordable 96-compound fragment library.

Gerhard Klebe, Manfred S Weiss, Xiaojie Wang, 2016, Acta crystallographica. Section F, Structural biology communications.

One Question, Multiple Answers: Biochemical and Biophysical Screening Methods Retrieve Deviating Fragment Hit Lists

Timo Krotzky, Gerhard Klebe, Nedyalka Radeva, 2015, ChemMedChem.