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Journal of Molecular Biology|April 24, 2007
Structural basis for a high affinity inhibitor bound to protein kinase MK2Roman C Hillig, Uwe Eberspaecher, Felipe Monteclaro, et al.Acta Crystallographica. Section D, Structural Biology|November 17, 2025
Polo-like kinase 1-inhibitor co-complex structures via the surface-entropy reduction approach and a DARPin-assisted approachUwe Eberspaecher, Arndt A Schmitz, Gerhard Siemeister, et al.Protein Science : a Publication of the Protein Society|November 30, 2006
Identifying protein construct variants with increased crystallization propensity--a case studyGuido A Malawski, Roman C Hillig, Felipe Monteclaro, et al.Cancers|January 18, 2020
Characterization of the Menin-MLL Interaction as Therapeutic Cancer TargetKrzysztof Brzezinka, Ekaterina Nevedomskaya, Ralf Lesche, et al.Acta Crystallographica. Section D, Biological Crystallography|April 9, 2008
Structure of wild-type Plk-1 kinase domain in complex with a selective DARPinTiago M Bandeiras, Roman Christian Hillig, Pedro M Matias, et al.Journal of Medicinal Chemistry|December 20, 2018
Discovery and Characterization of the Potent and Highly Selective (Piperidin-4-yl)pyrido[3,2- d]pyrimidine Based in Vitro Probe BAY-885 for the Kinase ERK5Duy Nguyen, Clara Lemos, Lars Wortmann, et al.Bioconjugate Chemistry|June 6, 2022
A Novel NAMPT Inhibitor-Based Antibody-Drug Conjugate Payload Class for Cancer TherapyNiels Böhnke, Markus Berger, Nils Griebenow, et al.Journal of Medicinal Chemistry|April 28, 2020
Treating Cancer by Spindle Assembly Checkpoint Abrogation: Discovery of Two Clinical Candidates, BAY 1161909 and BAY 1217389, Targeting MPS1 KinaseVolker K Schulze, Ulrich Klar, Dirk Kosemund, et al.Pageof 1