Structural coupling of SH2-kinase domains links Fes and Abl substrate recognition and kinase activation. Read more about Structural coupling of SH2-kinase domains links Fes and Abl substrate recognition and kinase activation.
A pilot project to generate affinity reagents to human proteins. Read more about A pilot project to generate affinity reagents to human proteins.
Building skeletally diverse architectures on the Indoline Scaffold: the discovery of a chemical probe of focal adhesion kinase signaling networks. Read more about Building skeletally diverse architectures on the Indoline Scaffold: the discovery of a chemical probe of focal adhesion kinase signaling networks.
Inhibitor scaffolds for 2-oxoglutarate-dependent histone lysine demethylases. Read more about Inhibitor scaffolds for 2-oxoglutarate-dependent histone lysine demethylases.
Structural basis and specificity of human otubain 1-mediated deubiquitination. Read more about Structural basis and specificity of human otubain 1-mediated deubiquitination.
Short-term glucocorticoid treatment increases insulin secretion in islets derived from lean mice through multiple pathways and mechanisms. Read more about Short-term glucocorticoid treatment increases insulin secretion in islets derived from lean mice through multiple pathways and mechanisms.
Structural basis for parasite-specific functions of the divergent profilin of Plasmodium falciparum. Read more about Structural basis for parasite-specific functions of the divergent profilin of Plasmodium falciparum.
Structure-activity relationships of human AKR-type oxidoreductases involved in bile acid synthesis: AKR1D1 and AKR1C4. Read more about Structure-activity relationships of human AKR-type oxidoreductases involved in bile acid synthesis: AKR1D1 and AKR1C4.
The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative. Read more about The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative.
Structural insights into the inhibited states of the Mer receptor tyrosine kinase. Read more about Structural insights into the inhibited states of the Mer receptor tyrosine kinase.