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Structure, mechanism and crystallographic fragment screening of the SARS-CoV-2 NSP13 helicase.

  • Read more about Structure, mechanism and crystallographic fragment screening of the SARS-CoV-2 NSP13 helicase.

Assessing reversible and irreversible binding effects of kinase covalent inhibitors through ADP-Glo assays.

  • Read more about Assessing reversible and irreversible binding effects of kinase covalent inhibitors through ADP-Glo assays.

Quantitative Methods to Study Protein Arginine Methyltransferase 1-9 Activity in Cells.

  • Read more about Quantitative Methods to Study Protein Arginine Methyltransferase 1-9 Activity in Cells.

Structural and functional characterization of ubiquitin variant inhibitors for the JAMM-family deubiquitinases STAMBP and STAMBPL1.

  • Read more about Structural and functional characterization of ubiquitin variant inhibitors for the JAMM-family deubiquitinases STAMBP and STAMBPL1.

Structure and Function of Protein Arginine Methyltransferase PRMT7.

  • Read more about Structure and Function of Protein Arginine Methyltransferase PRMT7.

Non-canonical role of Hippo tumor suppressor serine/threonine kinase 3 STK3 in prostate cancer.

  • Read more about Non-canonical role of Hippo tumor suppressor serine/threonine kinase 3 STK3 in prostate cancer.

Discovery of a Potent Dual SLK/STK10 Inhibitor Based on a Maleimide Scaffold.

  • Read more about Discovery of a Potent Dual SLK/STK10 Inhibitor Based on a Maleimide Scaffold.

A NSD3-targeted PROTAC suppresses NSD3 and cMyc oncogenic nodes in cancer cells.

  • Read more about A NSD3-targeted PROTAC suppresses NSD3 and cMyc oncogenic nodes in cancer cells.

Development of a Selective Dual Discoidin Domain Receptor (DDR)/p38 Kinase Chemical Probe.

  • Read more about Development of a Selective Dual Discoidin Domain Receptor (DDR)/p38 Kinase Chemical Probe.

Novel quaternary structures of the human prion protein globular domain.

  • Read more about Novel quaternary structures of the human prion protein globular domain.

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