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环磷酸腺苷受体蛋白的DNA相互作用位点的分子模型。

Molecuar model of the DNA interaction site for the cyclic AMP receptor protein.

作者信息

O'Neill M C, Amass K, de Crombrugghe B

出版信息

Proc Natl Acad Sci U S A. 1981 Apr;78(4):2213-7. doi: 10.1073/pnas.78.4.2213.

Abstract

A topological model of the DNA binding site for the cyclic AMP receptor protein (CRP) is presented. A consensus sequence drawn from the known CRP binding sites has several symmetrical subregions that are spatially resolved onto different faces of the DNA helix. Consideration of available biochemical and genetic data suggest one particular choice among the possible symmetrical arrangements. In this case, the sequence of its helical form presents nearly the same pattern of exposed base pairs on two faces of the helix. These two faces are separated by a helix angle of 72 degrees; the similar sequences that are exposed in the grooves occur in opposite orientations on the two faces. We propose that this inverted symmetry arrangement provides each of the identical subunits of the CRP with a similar recognition region within the overall site. In gal and ara, the site appears to accommodate a single molecule of the CRP; in lac, the site repeats the symmetrical arrangement and should accommodate two molecules of the CRP.

摘要

本文提出了一种环磷酸腺苷受体蛋白(CRP)的DNA结合位点的拓扑模型。从已知的CRP结合位点得出的共有序列有几个对称亚区域,这些亚区域在空间上解析到DNA螺旋的不同面上。对现有生化和遗传数据的考虑表明,在可能的对称排列中有一个特定的选择。在这种情况下,其螺旋形式的序列在螺旋的两个面上呈现出几乎相同的暴露碱基对模式。这两个面被72度的螺旋角隔开;在凹槽中暴露的相似序列在两个面上以相反的方向出现。我们提出,这种反向对称排列为CRP的每个相同亚基在整个位点内提供了一个相似的识别区域。在gal和ara中,该位点似乎容纳单个CRP分子;在lac中,该位点重复对称排列,应该容纳两个CRP分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a79/319314/4bbab939cc38/pnas00655-0257-a.jpg

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