Search

Structural class is an important attribute of protein, which plays an important role in both the experiment and theoretical research of protein science. Prediction of protein structural classes has been a challenging task, specifically for low-similarity datasets. In this paper, we develop a feature extraction method PSSS-SOMA-PSSM by incorporating two different modes of evolutionary information into Chou's general pseudo amino acid composition (PseAAC) based on predicted secondary structure sequence (PSSS) and position-specific scoring matrix (PSSM). We construct a 170-dimensional (170D) feature vector for each protein sequence sample, which contains 10D PSSS features that reflect content, alternating word frequency and novel position information, and contains 160D PSSM features that are calculated by second-order moving average (SOMA) algorithm. The SVM classifier with RBF kernel function and the jackknife test are used to predict and evaluate on 1189, 25PDB and 640 datasets with sequence similarity lower than 40%, 25%, and 25%, respectively. Comparison of our results with other methods shows that the proposed method provides the state-of-the-art performance and a cost-effective alternative to structural classes prediction for low-similarity datasets. [ABSTRACT FROM AUTHOR]

Abstract: Prediction of protein structural class for low-similarity sequences remains a challenging problem. In this study, the new computational method has been developed to predict protein structural class by incorporating alternating word frequency and normalized Lempel–Ziv complexity. To evaluate the performance of the proposed method, jackknife cross-validation tests are performed on three widely used benchmark datasets, 25PDB, 1189 and 640, respectively. We report 83.6%, 81.8% and 83.6% prediction accuracies for 25PDB, 1189 and 640 benchmarks, respectively. Comparison of our results with other methods shows that the proposed method is very promising and may provide a cost-effective alternative to predict protein structural class in particular for low-similarity datasets and may at least play an important complementary role to existing methods. [Copyright &y& Elsevier]

Prediction of protein structural classes for low-similarity sequences is useful for understanding fold patterns, regulation, functions, and interactions of proteins. It is well known that feature extraction is significant to prediction of protein structural class and it mainly uses protein primary sequence, predicted secondary structure sequence, and position-specific scoring matrix (PSSM). Currently, prediction solely based on the PSSM has played a key role in improving the prediction accuracy. In this paper, we propose a novel method called CSP-SegPseP-SegACP by fusing consensus sequence (CS), segmented PsePSSM, and segmented autocovariance transformation (ACT) based on PSSM. Three widely used low-similarity datasets (1189, 25PDB, and 640) are adopted in this paper. Then a 700-dimensional (700D) feature vector is constructed and the dimension is decreased to 224D by using principal component analysis (PCA). To verify the performance of our method, rigorous jackknife cross-validation tests are performed on 1189, 25PDB, and 640 datasets. Comparison of our results with the existing PSSM-based methods demonstrates that our method achieves the favorable and competitive performance. This will offer an important complementary to other PSSM-based methods for prediction of protein structural classes for low-similarity sequences. [ABSTRACT FROM AUTHOR]