Faculty of Life Sciences, The University of Manchester, Michael Smith Building, Oxford Road, Manchester M13 9PT, UK.
BMC Bioinformatics. 2009 Nov 18;10:379. doi: 10.1186/1471-2105-10-379.
The rate of protein structures being deposited in the Protein Data Bank surpasses the capacity to experimentally characterise them and therefore computational methods to analyse these structures have become increasingly important. Identifying the region of the protein most likely to be involved in function is useful in order to gain information about its potential role. There are many available approaches to predict functional site, but many are not made available via a publicly-accessible application.
Here we present a functional site prediction tool (SitesIdentify), based on combining sequence conservation information with geometry-based cleft identification, that is freely available via a web-server. We have shown that SitesIdentify compares favourably to other functional site prediction tools in a comparison of seven methods on a non-redundant set of 237 enzymes with annotated active sites.
SitesIdentify is able to produce comparable accuracy in predicting functional sites to its closest available counterpart, but in addition achieves improved accuracy for proteins with few characterised homologues. SitesIdentify is available via a webserver at http://www.manchester.ac.uk/bioinformatics/sitesidentify/
蛋白质结构在蛋白质数据库中的沉积速度超过了实验特性化的速度,因此分析这些结构的计算方法变得越来越重要。为了获得关于其潜在作用的信息,识别蛋白质中最有可能涉及功能的区域是很有用的。有许多可用的方法来预测功能位点,但许多方法无法通过公共可访问的应用程序获得。
在这里,我们提出了一种基于序列保守性信息与基于几何的裂缝识别相结合的功能位点预测工具(SitesIdentify),该工具可通过网络服务器免费获得。我们已经证明,在对 237 个具有注释活性位点的非冗余酶组进行的七种方法的比较中,SitesIdentify 与其他功能位点预测工具相比具有优势。
SitesIdentify 能够在预测功能位点方面与最接近的同类工具相媲美,但对于具有较少特征同源物的蛋白质,它还能实现更高的准确性。SitesIdentify 可通过网络服务器访问,网址为 http://www.manchester.ac.uk/bioinformatics/sitesidentify/