Taylor Paul D, Attwood Teresa K, Flower Darren R
The Jenner Institute, University of Oxford, Compton,Newbury, Berkshire, RG20 7NN, UK.
Bioinformation. 2006 Dec 2;1(8):276-80. doi: 10.6026/97320630001276.
Based on Bayesian Networks, methods were created that address protein sequence-based bacterial subcellular location prediction. Distinct predictive algorithms for the eight bacterial subcellular locations were created. Several variant methods were explored. These variations included differences in the number of residues considered within the query sequence - which ranged from the N-terminal 10 residues to the whole sequence - and residue representation - which took the form of amino acid composition, percentage amino acid composition, or normalised amino acid composition. The accuracies of the best performing networks were then compared to PSORTB. All individual location methods outperform PSORTB except for the Gram+ cytoplasmic protein predictor, for which accuracies were essentially equal, and for outer membrane protein prediction, where PSORTB outperforms the binary predictor. The method described here is an important new approach to method development for subcellular location prediction. It is also a new, potentially valuable tool for candidate subunit vaccine selection.
基于贝叶斯网络,创建了用于解决基于蛋白质序列的细菌亚细胞定位预测的方法。针对八个细菌亚细胞定位创建了不同的预测算法。探索了几种变体方法。这些变体包括查询序列中考虑的残基数的差异(范围从N端的10个残基到整个序列)以及残基表示形式(采用氨基酸组成、氨基酸组成百分比或归一化氨基酸组成的形式)。然后将性能最佳的网络的准确性与PSORTB进行比较。除了革兰氏阳性细胞质蛋白预测器(其准确性基本相当)和外膜蛋白预测(PSORTB在此方面优于二元预测器)外,所有单个定位方法均优于PSORTB。这里描述的方法是亚细胞定位预测方法开发的一种重要新方法。它也是用于候选亚单位疫苗选择的一种新的、潜在有价值的工具。