<p>The Kinase-Ligand Interaction Fingerprints and Structure database (KLIFS) contains a consistent structural alignment and deconstruction of the kinase domains from over 1734 PDB structures covering 190 different human kinases. </p> <p>Every crystal structure was structurally aligned in a consistent manner, subsequently broken down from the full complex into separate structural parts: the protein, the orthosteric ligand-binding pocket (85 aligned residues covering the catalytic cleft), orthosteric and allosteric ligand(s), ions, organometallics, cofactors, and waters. By combining the pocket with the orthosteric ligand all interactions are annotated using Interactions FingerPrints (IFPs) for systematic comparison.</p
International audienceBiological matter is organized in functional networks of different natures amo...
Successful kinase inhibitor drug discovery relies heavily on the structural knowledge of the interac...
Abstract Background Phosphorylation events direct the flow of signals and metabolites along cellular...
The Kinase-Ligand Interaction Fingerprints and Structure database (KLIFS) contains a consistent stru...
Protein kinases play a crucial role in cell signaling and are important drug targets in several ther...
Kinases are a prime target of drug development efforts with >60 drug approvals in the past two decad...
Targeted polypharmacology of kinases has emerged as a promising strategy to design efficient and saf...
The human protein kinase superfamily consists of over 500 members that individually control specific...
Protein structure determination of soluble globular protein domains has developed into an efficient ...
BackgroundProtein sequence similarity is a commonly used criterion for inferring the unknown functio...
Protein kinases are an important class of enzymes involved in the phosphorylation of their targets, ...
AbstractProtein structure determination of soluble globular protein domains has developed into an ef...
The human proteome is rich with protein kinases, and this richness has made the kinase of crucial im...
The aberrant activation of protein kinases is associated with many human diseases, most notably canc...
Kinase-targeted drug design is challenging. It requires designing inhibitors that can bind to specif...
International audienceBiological matter is organized in functional networks of different natures amo...
Successful kinase inhibitor drug discovery relies heavily on the structural knowledge of the interac...
Abstract Background Phosphorylation events direct the flow of signals and metabolites along cellular...
The Kinase-Ligand Interaction Fingerprints and Structure database (KLIFS) contains a consistent stru...
Protein kinases play a crucial role in cell signaling and are important drug targets in several ther...
Kinases are a prime target of drug development efforts with >60 drug approvals in the past two decad...
Targeted polypharmacology of kinases has emerged as a promising strategy to design efficient and saf...
The human protein kinase superfamily consists of over 500 members that individually control specific...
Protein structure determination of soluble globular protein domains has developed into an efficient ...
BackgroundProtein sequence similarity is a commonly used criterion for inferring the unknown functio...
Protein kinases are an important class of enzymes involved in the phosphorylation of their targets, ...
AbstractProtein structure determination of soluble globular protein domains has developed into an ef...
The human proteome is rich with protein kinases, and this richness has made the kinase of crucial im...
The aberrant activation of protein kinases is associated with many human diseases, most notably canc...
Kinase-targeted drug design is challenging. It requires designing inhibitors that can bind to specif...
International audienceBiological matter is organized in functional networks of different natures amo...
Successful kinase inhibitor drug discovery relies heavily on the structural knowledge of the interac...
Abstract Background Phosphorylation events direct the flow of signals and metabolites along cellular...