SALMON: solvent accessibility, ligand binding, and mapping of ligand orientation by NMR spectroscopy. Read more about SALMON: solvent accessibility, ligand binding, and mapping of ligand orientation by NMR spectroscopy.
A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases. Read more about A systematic interaction map of validated kinase inhibitors with Ser/Thr kinases.
Evaluation of micro-parallel liquid chromatography as a method for HTS-coupled actives verification. Read more about Evaluation of micro-parallel liquid chromatography as a method for HTS-coupled actives verification.
The use of systematic N- and C-terminal deletions to promote production and structural studies of recombinant proteins. Read more about The use of systematic N- and C-terminal deletions to promote production and structural studies of recombinant proteins.
Structure of the human protein kinase MPSK1 reveals an atypical activation loop architecture. Read more about Structure of the human protein kinase MPSK1 reveals an atypical activation loop architecture.
First crystallographic models of human TBC domains in the context of a family-wide structural analysis. Read more about First crystallographic models of human TBC domains in the context of a family-wide structural analysis.
Activation segment dimerization: a mechanism for kinase autophosphorylation of non-consensus sites. Read more about Activation segment dimerization: a mechanism for kinase autophosphorylation of non-consensus sites.
Bermuda Principles meet structural biology. Read more about Bermuda Principles meet structural biology.
Doing more than just the structure-structural genomics in kinase drug discovery. Read more about Doing more than just the structure-structural genomics in kinase drug discovery.
