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Robust and accurate prediction of self-interacting proteins from protein sequence information by exploiting weighted sparse representation based classifier.
Li, Yang; Hu, Xue-Gang; You, Zhu-Hong; Li, Li-Ping; Li, Pei-Pei; Wang, Yan-Bin; Huang, Yu-An.
Afiliación
  • Li Y; School of Computer Science and Information Engineering, Hefei University of Technology, Hefei, 230601, China.
  • Hu XG; School of Computer Science and Information Engineering, Hefei University of Technology, Hefei, 230601, China. jsjxhuxg@hfut.edu.cn.
  • You ZH; School of Computer Science, Northwestern Polytechnical University, Xi'an, 710129, Shaanxi, China. zhuhongyou@gmail.com.
  • Li LP; College of Grassland and Environment Sciences, Xinjiang Agricultural University, Urumqi, 830052, China.
  • Li PP; School of Computer Science and Information Engineering, Hefei University of Technology, Hefei, 230601, China.
  • Wang YB; School of Cyber Science and Technology, Zhejiang University, Hangzhou, 310027, China.
  • Huang YA; Guangxi Academy of Sciences, Nanning, 530007, Guangxi, China.
BMC Bioinformatics ; 23(Suppl 7): 518, 2022 Dec 01.
Article en En | MEDLINE | ID: mdl-36457083
BACKGROUND: Self-interacting proteins (SIPs), two or more copies of the protein that can interact with each other expressed by one gene, play a central role in the regulation of most living cells and cellular functions. Although numerous SIPs data can be provided by using high-throughput experimental techniques, there are still several shortcomings such as in time-consuming, costly, inefficient, and inherently high in false-positive rates, for the experimental identification of SIPs even nowadays. Therefore, it is more and more significant how to develop efficient and accurate automatic approaches as a supplement of experimental methods for assisting and accelerating the study of predicting SIPs from protein sequence information. RESULTS: In this paper, we present a novel framework, termed GLCM-WSRC (gray level co-occurrence matrix-weighted sparse representation based classification), for predicting SIPs automatically based on protein evolutionary information from protein primary sequences. More specifically, we firstly convert the protein sequence into Position Specific Scoring Matrix (PSSM) containing protein sequence evolutionary information, exploiting the Position Specific Iterated BLAST (PSI-BLAST) tool. Secondly, using an efficient feature extraction approach, i.e., GLCM, we extract abstract salient and invariant feature vectors from the PSSM, and then perform a pre-processing operation, the adaptive synthetic (ADASYN) technique, to balance the SIPs dataset to generate new feature vectors for classification. Finally, we employ an efficient and reliable WSRC model to identify SIPs according to the known information of self-interacting and non-interacting proteins. CONCLUSIONS: Extensive experimental results show that the proposed approach exhibits high prediction performance with 98.10% accuracy on the yeast dataset, and 91.51% accuracy on the human dataset, which further reveals that the proposed model could be a useful tool for large-scale self-interacting protein prediction and other bioinformatics tasks detection in the future.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biología Computacional / Evolución Biológica Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biología Computacional / Evolución Biológica Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: BMC Bioinformatics Asunto de la revista: INFORMATICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: China Pais de publicación: Reino Unido