Fragment Binding to the Nsp3 Macrodomain of SARS-CoV-2 Identified Through Crystallographic Screening and Computational Docking. Read more about Fragment Binding to the Nsp3 Macrodomain of SARS-CoV-2 Identified Through Crystallographic Screening and Computational Docking.
Discovery of a Novel Class of Covalent Dual Inhibitors Targeting the Protein Kinases BMX and BTK. Read more about Discovery of a Novel Class of Covalent Dual Inhibitors Targeting the Protein Kinases BMX and BTK.
Identification of lysine isobutyrylation as a new histone modification mark. Read more about Identification of lysine isobutyrylation as a new histone modification mark.
How to Separate Kinase Inhibition from Undesired Monoamine Oxidase A Inhibition-The Development of the DYRK1A Inhibitor AnnH75 from the Alkaloid Harmine. Read more about How to Separate Kinase Inhibition from Undesired Monoamine Oxidase A Inhibition-The Development of the DYRK1A Inhibitor AnnH75 from the Alkaloid Harmine.
Human MettL3-MettL14 complex is a sequence-specific DNA adenine methyltransferase active on single-strand and unpaired DNA in vitro. Read more about Human MettL3-MettL14 complex is a sequence-specific DNA adenine methyltransferase active on single-strand and unpaired DNA in vitro.
Molecular basis for ubiquitin ligase CRL2FEM1C-mediated recognition of C-degron. Read more about Molecular basis for ubiquitin ligase CRL2FEM1C-mediated recognition of C-degron.
The low-cost Shifter microscope stage transforms the speed and robustness of protein crystal harvesting. Read more about The low-cost Shifter microscope stage transforms the speed and robustness of protein crystal harvesting.
A High-Throughput RNA Displacement Assay for Screening SARS-CoV-2 nsp10-nsp16 Complex toward Developing Therapeutics for COVID-19. Read more about A High-Throughput RNA Displacement Assay for Screening SARS-CoV-2 nsp10-nsp16 Complex toward Developing Therapeutics for COVID-19.
The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification. Read more about The Kinase Chemogenomic Set (KCGS): An Open Science Resource for Kinase Vulnerability Identification.
BET inhibition disrupts transcription but retains enhancer-promoter contact. Read more about BET inhibition disrupts transcription but retains enhancer-promoter contact.
