Analysis of the dominant mutation N188T of human connexin46 (hCx46) using concatenation and molecular dynamics simulation

por Schadzek, Patrik, Stahl, Yannick, Preller, Matthias, Ngezahayo, Anaclet
Publicado 2019

Lipase-Catalyzed Chemoselective Ester Hydrolysis of Biomimetically Coupled Aryls for the Synthesis of Unsymmetric Biphenyl Esters

por Ehlert, Janna, Kronemann, Jenny, Zumbrägel, Nadine, Preller, Matthias
Publicado 2019

Structural and Computational Insights into a Blebbistatin-Bound Myosin•ADP Complex with Characteristics of an ADP-Release Conformation along the Two-Step Myosin Power Stoke

por Ewert, Wiebke, Franz, Peter, Tsiavaliaris, Georgios, Preller, Matthias
Publicado 2020

Unraveling a Force-Generating Allosteric Pathway of Actomyosin Communication Associated with ADP and P(i) Release

por Franz, Peter, Ewert, Wiebke, Preller, Matthias, Tsiavaliaris, Georgios
Publicado 2020

Correction: Franz et al. Unraveling a Force-Generating Allosteric Pathway of Actomyosin Communication Associated with ADP and P(i) Release. Int. J. Mol. Sci. 2021, 22, 104

por Franz, Peter, Ewert, Wiebke, Preller, Matthias, Tsiavaliaris, Georgios
Publicado 2022

Triiodothyronine Acts as a Smart Influencer on Hsp90 via a Triiodothyronine Binding Site

por Fan, Lu, Warnecke, Athanasia, Weder, Julia, Preller, Matthias, Zeilinger, Carsten
Publicado 2022

Mechanistic insights into the active site and allosteric communication pathways in human nonmuscle myosin-2C

por Chinthalapudi, Krishna, Heissler, Sarah M, Preller, Matthias, Sellers, James R, Manstein, Dietmar J
Publicado 2017

Small molecule-mediated refolding and activation of myosin motor function

por Radke, Michael B, Taft, Manuel H, Stapel, Britta, Hilfiker-Kleiner, Denise, Preller, Matthias, Manstein, Dietmar J
Publicado 2014

Data of the molecular dynamics simulations of mutations in the human connexin46 docking interface

por Schadzek, Patrik, Schlingmann, Barbara, Schaarschmidt, Frank, Lindner, Julia, Koval, Michael, Heisterkamp, Alexander, Ngezahayo, Anaclet, Preller, Matthias
Publicado 2016

Structural Basis for the Allosteric Interference of Myosin Function by Reactive Thiol Region Mutations G680A and G680V

por Preller, Matthias, Bauer, Stefanie, Adamek, Nancy, Fujita-Becker, Setsuko, Fedorov, Roman, Geeves, Michael A., Manstein, Dietmar J.
Publicado 2011

C-mannosylation supports folding and enhances stability of thrombospondin repeats

por Shcherbakova, Aleksandra, Preller, Matthias, Taft, Manuel H, Pujols, Jordi, Ventura, Salvador, Tiemann, Birgit, Buettner, Falk FR, Bakker, Hans
Publicado 2019

Recording Sodium Self-Inhibition of Epithelial Sodium Channels Using Automated Electrophysiology in Xenopus Oocytes

por Lawong, Rene Y., May, Fabian, Etang, Etang C., Vorrat, Philipp, George, Jonas, Weder, Julia, Kockler, Dagmar, Preller, Matthias, Althaus, Mike
Publicado 2023

Distinct Functional Interactions between Actin Isoforms and Nonsarcomeric Myosins

por Müller, Mirco, Diensthuber, Ralph P., Chizhov, Igor, Claus, Peter, Heissler, Sarah M., Preller, Matthias, Taft, Manuel H., Manstein, Dietmar J.
Publicado 2013

Pharmacological inhibitors of the cystic fibrosis transmembrane conductance regulator exert off-target effects on epithelial cation channels

por Lin, JinHeng, Gettings, Sean M., Talbi, Khaoula, Schreiber, Rainer, Taggart, Michael J., Preller, Matthias, Kunzelmann, Karl, Althaus, Mike, Gray, Michael A.
Publicado 2022

A role for actin flexibility in thin filament-mediated contractile regulation and myopathy

por Viswanathan, Meera C., Schmidt, William, Franz, Peter, Rynkiewicz, Michael J., Newhard, Christopher S., Madan, Aditi, Lehman, William, Swank, Douglas M., Preller, Matthias, Cammarato, Anthony
Publicado 2020

Identification of a Thyroid Hormone Binding Site in Hsp90 with Implications for Its Interaction with Thyroid Hormone Receptor Beta

por Fan, Lu, Kishore, Anusha, Jansen-Olliges, Linda, Wang, Dahua, Stahl, Frank, Psathaki, Olympia Ekaterini, Harre, Jennifer, Warnecke, Athanasia, Weder, Julia, Preller, Matthias, Zeilinger, Carsten
Publicado 2022

SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia

por Osmanovic, Alma, Widjaja, Maylin, Förster, Alisa, Weder, Julia, Wattjes, Mike P., Lange, Inken, Sarikidi, Anastasia, Auber, Bernd, Raab, Peter, Christians, Anne, Preller, Matthias, Petri, Susanne, Weber, Ruthild G.
Publicado 2020

Mechanism and Specificity of Pentachloropseudilin-mediated Inhibition of Myosin Motor Activity

por Chinthalapudi, Krishna, Taft, Manuel H., Martin, René, Heissler, Sarah M., Preller, Matthias, Hartmann, Falk K., Brandstaetter, Hemma, Kendrick-Jones, John, Tsiavaliaris, Georgios, Gutzeit, Herwig O., Fedorov, Roman, Buss, Folma, Knölker, Hans-Joachim, Coluccio, Lynne M., Manstein, Dietmar J.
Publicado 2011

In vivo efficacy of mutant IDH1 inhibitor HMS-101 and structural resolution of distinct binding site

por Chaturvedi, Anuhar, Goparaju, Ramya, Gupta, Charu, Weder, Julia, Klünemann, Thomas, Araujo Cruz, Michelle Maria, Kloos, Arnold, Goerlich, Kerstin, Schottmann, Renate, Othman, Basem, Struys, Eduard A., Bähre, Heike, Grote-Koska, Denis, Brand, Korbinian, Ganser, Arnold, Preller, Matthias, Heuser, Michael
Publicado 2019

Rare germline variants in the E-cadherin gene CDH1 are associated with the risk of brain tumors of neuroepithelial and epithelial origin

por Förster, Alisa, Brand, Frank, Banan, Rouzbeh, Hüneburg, Robert, Weber, Christine A. M., Ewert, Wiebke, Kronenberg, Jessica, Previti, Christopher, Elyan, Natalie, Beyer, Ulrike, Martens, Helge, Hong, Bujung, Bräsen, Jan H., Erbersdobler, Andreas, Krauss, Joachim K., Stangel, Martin, Samii, Amir, Wolf, Stephan, Preller, Matthias, Aretz, Stefan, Wiese, Bettina, Hartmann, Christian, Weber, Ruthild G.
Publicado 2021