机译:Thermostable homologues of the periplasmic siderophore‐binding protein CeuE from Geobacillus stearothermophilus and Parageobacillus thermoglucosidasius
机译:3D structures of the Plasmodium vivax subtilisin‐like drug target SUB1 reveal conformational changes to accommodate a substrate‐derived α‐ketoamide inhibitor
机译:Structural and biochemical insights into purine‐based drug molecules in hBRD2 delineate a unique binding mode opening new vistas in the design of inhibitors of the BET family