Abstract
The function of a protein is closely tied to its subcellular location. Identifying the subcellular location of proteins is a crucial step to understand their functions. However, determining the subcellular location of proteins experimentally is time-consuming and costly. Therefore, developing effective computational methods to predict the subcellular positions of proteins is a hotspot in bioinformatics. Though many models have been proposed to improve the prediction accuracy of protein subcellular localization, there are still several shortcomings: (1) numerous methods ignore the multi-site proteins; (2) high dimensional features bring the burden to the construction of the prediction model. In this work, we proposed a method to predict the subcellular location of bacterial proteins with both single and multiple locations. Two features based on evolutionary information are extracted to solve the multi-site prediction problem, of which one is a 190-dimensional feature vector from absolute entropy correlation analysis (AECA-PSSM) and another is a 480-dimensional feature vector extracted using discrete wavelet transform (PSSM-DWT). After combining both proposed features, multi-label linear discriminant analysis (MLDA) is employed to transform the high-dimensional feature space into a lower-dimensional space. Multi-label k-nearest neighbors algorithm (ML-KNN) is utilized to predict the subcellular location of both single-site and multi-site proteins. Experimental results on Gram-positive dataset and Gram-negative dataset show the effectiveness of the proposed method.
Highlights
The knowledge of subcellular location of proteins is very important which is closely associate with their function [1]
Consider the 2nd rule of Chou’s 5-steps rule [44], in this study, we propose to utilize two novel features extracted from position-specific scoring matrix (PSSM) to predict subcellular location of bacteria proteins
Feature fusion can solve the defect of insufficient information in using a single feature set, so that fusing features calculated by different algorithms becomes an effective method to improve the accuracy of protein subcellular localization prediction
Summary
The knowledge of subcellular location of proteins is very important which is closely associate with their function [1]. In 2015, Dehzangi et al [17] proposed two segmentation based feature extraction methods from PSSM to predict the subcellular location of Gram-positive and Gram-negative proteins. Using Gene Ontogy (GO) information as feature extraction methods to predict the subcellular location of proteins has been obtained a series of results [23]–[26].
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