Protein structure determination of soluble globular protein domains has developed into an efficient routine technology which can now be applied to generate and analyze structures of entire human protein families. In the kinase area, several kinase families still lack comprehensive structural analysis. Nevertheless, Structural Genomics (SG) efforts contributed more than 40 kinase catalytic domain structures during the past 4 years providing a rich resource of information for large scale comparisons of kinase active sites. Moreover, many of the released structures are inhibitor complexes that offer chemical starting points for development of selective and potent inhibitors. Here we discuss the currently available structural data and strategie...
Drug discovery programs frequently target members of the human kinome and try to identify small mole...
The human protein kinase superfamily consists of over 500 members that individually control specific...
Protein kinases are highly tractable targets for drug discovery. However, the biological function an...
AbstractProtein structure determination of soluble globular protein domains has developed into an ef...
AbstractProtein structure determination of soluble globular protein domains has developed into an ef...
Structural genomics (SG) has significantly increased the number of novel protein structures of targe...
Many protein kinases are validated intervention points for drug development, however active site sim...
Successful kinase inhibitor drug discovery relies heavily on the structural knowledge of the interac...
The aberrant activation of protein kinases is associated with many human diseases, most notably canc...
The aberrant activation of protein kinases is associated with many human diseases, most notably canc...
The human proteome is rich with protein kinases, and this richness has made the kinase of crucial im...
Protein kinases are key components in cellular signalling pathways as they carry out the phosphoryla...
Our current understanding of the structure, mechanism of action and modes of regulation of the prote...
Drug discovery programs frequently target members of the human kinome and try to identify small mole...
Publicly available kinase inhibitors provide a large source of information for structure–activity re...
Drug discovery programs frequently target members of the human kinome and try to identify small mole...
The human protein kinase superfamily consists of over 500 members that individually control specific...
Protein kinases are highly tractable targets for drug discovery. However, the biological function an...
AbstractProtein structure determination of soluble globular protein domains has developed into an ef...
AbstractProtein structure determination of soluble globular protein domains has developed into an ef...
Structural genomics (SG) has significantly increased the number of novel protein structures of targe...
Many protein kinases are validated intervention points for drug development, however active site sim...
Successful kinase inhibitor drug discovery relies heavily on the structural knowledge of the interac...
The aberrant activation of protein kinases is associated with many human diseases, most notably canc...
The aberrant activation of protein kinases is associated with many human diseases, most notably canc...
The human proteome is rich with protein kinases, and this richness has made the kinase of crucial im...
Protein kinases are key components in cellular signalling pathways as they carry out the phosphoryla...
Our current understanding of the structure, mechanism of action and modes of regulation of the prote...
Drug discovery programs frequently target members of the human kinome and try to identify small mole...
Publicly available kinase inhibitors provide a large source of information for structure–activity re...
Drug discovery programs frequently target members of the human kinome and try to identify small mole...
The human protein kinase superfamily consists of over 500 members that individually control specific...
Protein kinases are highly tractable targets for drug discovery. However, the biological function an...