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Identifying common structural DNA properties in transcription factor binding site sets of the LacI-GalR family

机译:鉴定LacI-GalR家族转录因子结合位点集中的常见结构DNA特性

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It is well known that transcription factors can induce deformations in their DNA-binding sites upon complex formation. However, few attempts have been made to investigate the extent to which induced structural deformations in the DNA molecule are conserved between different members of the same transcription factor family. In this article, we used the CRoSSeD methodology for describing DNA structural properties to extract common features in the binding sites of different LacI-GalR family members. The most significant feature identified in this way was located at the center of the binding sites, which is also the most likely location for an induced DNA deformation following an amino acid interdigitation. This feature was related further to specific elements present in the protein structure and was used to identify and characterize deviant family members. A general family-wide binding site model was constructed and applied to screen for unknown member binding sites.
机译:众所周知,转录因子可以在复合物形成后诱导其DNA结合位点变形。但是,很少有人尝试研究在同一转录因子家族的不同成员之间,DNA分子中诱导的结构变形的保守程度。在本文中,我们使用CRoSSeD方法描述DNA结构特性,以提取不同LacI-GalR家族成员结合位点的共有特征。以这种方式鉴定出的最重要的特征位于结合位点的中心,这也是在氨基酸互指后引起DNA变形的最可能的位置。此功能与蛋白质结构中存在的特定元素进一步相关,并用于鉴定和表征异常家族成员。构建了通用的全家族结合位点模型,并将其应用于筛选未知成员结合位点。

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