Fischer D
Dept. of Math and Computer Science, Faculty of Natural Science, Ben Gurion University, Beer-Sheva, Israel.
Pac Symp Biocomput. 2000:119-30.
Recent assessments of structure prediction have demonstrated that (i) although fold recognition methods can often identify remote similarities when standard sequence search methods fail, the score of the top-ranking fold is not always significant enough to allow a confident prediction; (ii) the use of structural information such as secondary structure increases recognition accuracy; (iii) modern sequence-based methods incorporating evolutionary information from neighboring sequences can often identify very remote similarities; (iv) there is no one single method that is superior to other methods when evaluated over a wide range of targets, and (v) extensive human-expert intervention is usually required for the most difficult prediction targets. Here, I describe a new, hybrid fold recognition method that incorporates structural and evolutionary information into a single fully automated method. This work is a first attempt towards the automation of some of the processes that are often applied by human predictors. The method is tested with two cases that are often applied by human predictors. The method is tested with two fold-recognition benchmarks demonstrating a superior performance. The higher sensitivity and selectivity enable the applicability of this method at genomic scales.
(i)尽管当标准序列搜索方法失效时,折叠识别方法常常能够识别出远亲相似性,但排名最高的折叠得分并不总是足够显著到可以做出可靠的预测;(ii)使用诸如二级结构等结构信息可提高识别准确率;(iii)纳入来自相邻序列进化信息的现代基于序列的方法常常能够识别出非常远的相似性;(iv)在对广泛的目标进行评估时,没有一种方法优于其他方法;(v)对于最难的预测目标,通常需要大量人类专家的干预。在此,我描述一种新的混合折叠识别方法,该方法将结构和进化信息整合到一个完全自动化的单一方法中。这项工作是朝着实现一些人类预测者常用流程的自动化迈出的第一步。该方法通过人类预测者常用的两个案例进行了测试。该方法在两个折叠识别基准测试中进行了测试,展现出卓越的性能。更高的灵敏度和选择性使得该方法在基因组规模上具有适用性。