Structural analysis of PIM1 kinase complexes with ATP-competitive inhibitors

por Bogusz, Jozefina, Zrubek, Karol, Rembacz, Krzysztof P., Grudnik, Przemyslaw, Golik, Przemyslaw, Romanowska, Malgorzata, Wladyka, Benedykt, Dubin, Grzegorz
Publicado 2017

Modular endolysin of Burkholderia AP3 phage has the largest lysozyme-like catalytic subunit discovered to date and no catalytic aspartate residue

por Maciejewska, Barbara, Źrubek, Karol, Espaillat, Akbar, Wiśniewska, Magdalena, Rembacz, Krzysztof P., Cava, Felipe, Dubin, Grzegorz, Drulis-Kawa, Zuzanna
Publicado 2017

Difluoromethyl-1,3,4-oxadiazoles are slow-binding substrate analog inhibitors of histone deacetylase 6 with unprecedented isotype selectivity

por Cellupica, Edoardo, Caprini, Gianluca, Cordella, Paola, Cukier, Cyprian, Fossati, Gianluca, Marchini, Mattia, Rocchio, Ilaria, Sandrone, Giovanni, Vanoni, Maria Antonietta, Vergani, Barbara, Źrubek, Karol, Stevenazzi, Andrea, Steinkühler, Christian
Publicado 2022