Journal of the American Chemical Society · 2007 · 34 citations · 10 references
Life SciencesBiologyMolecular BiologyProtein-protein InteractionsStructural BiologyStructural BiophysicsLigand BindingRna StructureRna-binding ProteinsRna-protein InteractionsStructural Basis Of RecognitionBinding AssaysLocal Sequence Context EffectsProtein-rna InterfacesProtein-rna Recognition MotifsProtein-rna Recognition SpecificityRna-binding Domain StructureRna-binding DomainsRna-binding Specificity
We describe a method to analyze the sequence specificity of an RNA-binding domain. The method, which we have named scaffold-independent analysis, reports on the specificity for each nucleotide position within an RNA target, uncoupled from the surrounding structural and sequence context. We expect this information to improve our understanding of protein-RNA interfaces in ssRNA binding domains (e.g., KH or RRM domains) and to be useful to the design of novel protein-RNA recognition surfaces. Our NMR binding assays using the third KH domain of the Nova-1 protein provide a proof-of-principle for the method and novel information on the specificity of this domain for its RNA targets.
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SMART 5: domains in the context of genomes and networks
Ivica Letunić · Nucleic Acids Research · 2005 · 968 citations · Full text
Sequence-Specific RNA Binding by a Nova KH Domain
H.A. Lewis, Kirk B. Jensen, Carme Edo et al. · Cell · 2000 · 328 citations · Full text
Nonsteroidal Anti-Inflammatory Drugs Can Lower Amyloidogenic Aß <sub>42</sub> by Inhibiting Rho
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