Comprehensive Structural and Functional Characterization of the Human Kinome by Protein Structure Modeling and Ligand Virtual Screening
- 20 September 2010
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of Chemical Information and Modeling
- Vol. 50 (10) , 1839-1854
- https://doi.org/10.1021/ci100235n
Abstract
The growing interest in the identification of kinase inhibitors, promising therapeutics in the treatment of many diseases, has created a demand for the structural characterization of the entire human kinome. At the outset of the drug development process, the lead-finding stage, approaches that enrich the screening library with bioactive compounds are needed. Here, protein structure based methods can play an important role, but despite structural genomics efforts, it is unlikely that the three-dimensional structures of the entire kinome will be available soon. Therefore, at the proteome level, structure-based approaches must rely on predicted models, with a key issue being their utility in virtual ligand screening. In this study, we employ the recently developed FINDSITE/Q-Dock ligand homology modeling approach, which is well-suited for proteome-scale applications using predicted structures, to provide extensive structural and functional characterization of the human kinome. Specifically, we construct structure models for the human kinome; these are subsequently subject to virtual screening against a library of more than 2 million compounds. To rank the compounds, we employ a hierarchical approach that combines ligand- and structure-based filters. Modeling accuracy is carefully validated using available experimental data with particularly encouraging results found for the ability to identify, without prior knowledge, specific kinase inhibitors. More generally, the modeling procedure results in a large number of predicted molecular interactions between kinases and small ligands that should be of practical use in the development of novel inhibitors. The data set is freely available to the academic community via a user-friendly Web interface at http://cssb.biology.gatech.edu/kinomelhm/ as well as at the ZINC Web site (http://zinc.docking.org/applications/2010Apr/Brylinski-2010.tar.gz).Keywords
This publication has 120 references indexed in Scilit:
- Identification of a novel inhibitor of JAK2 tyrosine kinase by structure-based virtual screeningBioorganic & Medicinal Chemistry Letters, 2009
- Directed Discovery of Agents Targeting the Met Tyrosine Kinase Domain by Virtual ScreeningJournal of Medicinal Chemistry, 2009
- Q‐Dock: Low‐resolution flexible ligand docking with pocket‐specific threading restraintsJournal of Computational Chemistry, 2008
- Fast procedure for reconstruction of full‐atom protein models from reduced representationsJournal of Computational Chemistry, 2008
- Assessment of programs for ligand binding affinity predictionJournal of Computational Chemistry, 2008
- Structural genomics: keeping up with expanding knowledge of the protein universeCurrent Opinion in Structural Biology, 2007
- Prediction of side‐chain conformations on protein surfacesProteins-Structure Function and Bioinformatics, 2007
- Benchmarking Sets for Molecular DockingJournal of Medicinal Chemistry, 2006
- The Blue Obelisk—Interoperability in Chemical InformaticsJournal of Chemical Information and Modeling, 2006
- UCSF Chimera—A visualization system for exploratory research and analysisJournal of Computational Chemistry, 2004