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

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Summary

Introduction

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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