Protein structure-based drug design: from docking to molecular dynamics von Śledź, Paweł, Caflisch, Amedeo

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Structural insights into the molecular mechanism of the m(6)A writer complex von Śledź, Paweł, Jinek, Martin

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Small‐Molecule Inhibitors of METTL3, the Major Human Epitranscriptomic Writer von Bedi, Rajiv K., Huang, Danzhi, Eberle, Stefanie A., Wiedmer, Lars, Śledź, Pawel, Caflisch, Amedeo

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Deep classification of a large cryo-EM dataset defines the conformational landscape of the 26S proteasome von Unverdorben, Pia, Beck, Florian, Śledź, Pawel, Schweitzer, Andreas, Pfeifer, Günter, Plitzko, Jürgen M., Baumeister, Wolfgang, Förster, Friedrich

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Flexible Binding of m6A Reader Protein YTHDC1 to Its Preferred RNA Motif von Li, Yaozong, Bedi, Rajiv Kumar, Wiedmer, Lars, Huang, Danzhi, Śledź, Paweł, Caflisch, Amedeo

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Structure of the 26S proteasome with ATP-γS bound provides insights into the mechanism of nucleotide-dependent substrate translocation von Śledź, Paweł, Unverdorben, Pia, Beck, Florian, Pfeifer, Günter, Schweitzer, Andreas, Förster, Friedrich, Baumeister, Wolfgang

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A three-stage biophysical screening cascade for fragment-based drug discovery von Mashalidis, Ellene H, Śledź, Paweł, Lang, Steffen, Abell, Chris

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Protein structure-based drug design: from docking to molecular dynamics von Śledź, Pawel, Caflisch, Amedeo

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Structure-Driven Developments of 26S Proteasome Inhibitors von led, Pawe, Baumeister, Wolfgang

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Crystal structure of the proteasomal deubiquitylation module Rpn8-Rpn11 von Pathare, Ganesh Ramnath, Nagy, István, Śledź, Paweł, Anderson, Daniel J., Zhou, Han-Jie, Pardon, Els, Steyaert, Jan, Förster, Friedrich, Bracher, Andreas, Baumeister, Wolfgang

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Rational Design and Evaluation of Upgraded Grubbs/Hoveyda Olefin Metathesis Catalysts: Polyfunctional Benzylidene Ethers on the Test Bench von Bieniek, Michał, Samojłowicz, Cezary, Sashuk, Volodymyr, Bujok, Robert, Śledź, Paweł, Lugan, Noël, Lavigne, Guy, Arlt, Dieter, Grela, Karol

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A Reader-Based Assay for m6A Writers and Erasers von Wiedmer, Lars, Eberle, Stefanie Alexandra, Bedi, Rajiv Kumar, Śledź, Paweł, Caflisch, Amedeo

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Structural insights into the molecular mechanism of the m6A writer complex von Śledź, Paweł, Jinek, Martin

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Ligand retargeting by binding site analogy von Wiedmer, Lars, Schärer, Claude, Spiliotopoulos, Dimitrios, Hürzeler, Marianne, Śledź, Paweł, Caflisch, Amedeo

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Binding Motifs in the CBP Bromodomain: An Analysis of 20 Crystal Structures of Complexes with Small Molecules von Zhu, Jian, Dong, Jing, Batiste, Laurent, Unzue, Andrea, Dolbois, Aymeric, Pascanu, Vlad, Śledź, Paweł, Nevado, Cristina, Caflisch, Amedeo

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From Crystal Packing to Molecular Recognition: Prediction and Discovery of a Binding Site on the Surface of Polo-Like Kinase 1 von Śledź, Paweł, Stubbs, Christopher J., Lang, Steffen, Yang, Yong-Qing, McKenzie, Grahame J., Venkitaraman, Ashok R., Hyvönen, Marko, Abell, Chris

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Hitting a Moving Target: Simulation and Crystallography Study of ATAD2 Bromodomain Blockers von Dolbois, Aymeric, Batiste, Laurent, Wiedmer, Lars, Dong, Jing, Brütsch, Manuela, Huang, Danzhi, Deerain, Nicholas M, Spiliotopoulos, Dimitrios, Cheng-Sánchez, Iván, Laul, Eleen, Nevado, Cristina, Śledź, Paweł, Caflisch, Amedeo

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High-Throughput Interrogation of Ligand Binding Mode Using a Fluorescence-Based Assay von Śledź, Paweł, Lang, Steffen, Stubbs, Christopher J., Abell, Chris

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Twenty Years After Communism: The Methodological Review von Sledz, Andrzej Pawel

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Olefin metathesis in ionic liquids von Sledź, Paweł, Mauduit, Marc, Grela, Karol

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