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An enriched structural kinase database to enable kinome‐wide structure‐based analyses and drug discovery
Authors:Natasja Brooijmans  Yu‐Wei Chang  Dominick Mobilio  Rajiah A. Denny  Christine Humblet
Affiliation:1. Chemical Sciences, Wyeth Research, Pearl River, New York 10965;2. Chemical Sciences, Wyeth Research, Cambridge, Massachusetts 02140;3. Chemical Sciences, Wyeth Research, Princeton, New Jersey 08543
Abstract:The development of a kinase structural database, the kinase knowledge base (KKB), is described. It covers all human kinase domain structures that have been deposited in the Protein Data Bank. All structures are renumbered using a common scheme, which enables efficient cross‐comparisons and multiple queries of interest to the kinase field. The common numbering scheme is also used to automatically annotate conserved residues and motifs, and conformationally classify the structures based on the DFG‐loop and Helix C. Analyses of residue conservation in the ATP binding site using the full human‐kinome–sequence alignment lead to the identification of a conserved hydrogen bond between the hinge region backbone and a glycine in the specificity surface. Furthermore, 90% of kinases are found to have at least one stabilizing interaction for the hinge region, which has not been described before.
Keywords:protein kinases  structure‐based drug design  crystallography: X‐ray  structural informatics  binding sites  databases: protein  protein conformation  catalytic domain  sequence analysis: protein  protein binding
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