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Williams–Beuren syndrome, characterized by numerous physiological and mental problems, is caused by the heterozygous deletion of chromosome region 7q11.23, which results in the disappearance of 26 protein‐coding genes. Protein WBSCR27 is a product of one of these genes whose biological function has not yet been established and for which structural information has been absent until now. Using NMR,...
Characterization of intrinsically disordered proteins (IDPs) has grown tremendously over the past two decades. NMR‐based structural characterization has been widely embraced by the IDP community, largely because this technique is amenable to highly flexible biomolecules. Particularly, carbon‐detect nuclear magnetic resonance (NMR) experiments provide a straight forward and expedient method for completing...
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