Vital-IT Group, SIB Swiss Institute of Bioinformatics, Lausanne, Switzerland.
BMC Bioinformatics. 2012 Jul 23;13:173. doi: 10.1186/1471-2105-13-173.
Today, recognition and classification of sequence motifs and protein folds is a mature field, thanks to the availability of numerous comprehensive and easy to use software packages and web-based services. Recognition of structural motifs, by comparison, is less well developed and much less frequently used, possibly due to a lack of easily accessible and easy to use software.
In this paper, we describe an extension of DeepView/Swiss-PdbViewer through which structural motifs may be defined and searched for in large protein structure databases, and we show that common structural motifs involved in stabilizing protein folds are present in evolutionarily and structurally unrelated proteins, also in deeply buried locations which are not obviously related to protein function.
The possibility to define custom motifs and search for their occurrence in other proteins permits the identification of recurrent arrangements of residues that could have structural implications. The possibility to do so without having to maintain a complex software/hardware installation on site brings this technology to experts and non-experts alike.
如今,由于大量全面且易于使用的软件包和基于网络的服务的出现,序列基序和蛋白质折叠的识别和分类已成为一个成熟的领域。相比之下,结构基序的识别则不太发达,也很少被使用,这可能是由于缺乏易于访问和使用的软件。
在本文中,我们描述了 DeepView/Swiss-PdbViewer 的扩展,通过该扩展可以在大型蛋白质结构数据库中定义和搜索结构基序,并且我们表明,参与稳定蛋白质折叠的常见结构基序存在于进化上和结构上不相关的蛋白质中,也存在于深度埋藏的位置,这些位置与蛋白质功能没有明显关系。
定义自定义基序并搜索它们在其他蛋白质中的出现的可能性允许识别可能具有结构意义的残基的重复排列。无需在现场维护复杂的软件/硬件安装即可实现这种可能性,使该技术能够为专家和非专家所使用。