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Identifying DNA-binding proteins using structural motifs and the electrostatic potential

机译:使用结构图案和静电势识别DNA结合蛋白

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Robust methods to detect DNA-binding proteins from structures of unknown function are important for structural biology. This paper describes a method for identifying such proteins that (i) have a solvent accessible structural motif necessary for DNA-binding and (ii) a positive electrostatic potential in the region of the binding region. We focus on three structural motifs: helix–turn-helix (HTH), helix–hairpin–helix (HhH) and helix–loop–helix (HLH). We find that the combination of these variables detect 78% of proteins with an HTH motif, which is a substantial improvement over previous work based purely on structural templates and is comparable to more complex methods of identifying DNA-binding proteins. Similar true positive fractions are achieved for the HhH and HLH motifs. We see evidence of wide evolutionary diversity for DNA-binding proteins with an HTH motif, and much smaller diversity for those with an HhH or HLH motif.
机译:从功能未知的结构中检测DNA结合蛋白的可靠方法对于结构生物学很重要。本文介绍了一种鉴定这种蛋白质的方法,该蛋白质具有(i)具有DNA结合所必需的溶剂可及的结构基序,以及(ii)在结合区区域具有正静电势。我们专注于三个结构基序:螺旋-转-螺旋(HTH),螺旋-发夹-螺旋(HhH)和螺旋-环-螺旋(HLH)。我们发现这些变量的组合检测到78%的具有HTH主题的蛋白质,这是对以前仅基于结构模板的工作的实质性改进,可与识别DNA结合蛋白的更复杂方法相媲美。 HhH和HLH基序获得了相似的真实阳性分数。我们看到具有HTH主题的DNA结合蛋白具有广泛的进化多样性,而具有HhH或HLH主题的蛋白具有更小的多样性。

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