4.7 Article

SSKM_Succ: A Novel Succinylation Sites Prediction Method Incorporating K-Means Clustering With a New Semi-Supervised Learning Algorithm

Publisher

IEEE COMPUTER SOC
DOI: 10.1109/TCBB.2020.3006144

Keywords

Succinylation; neurodegenerative diseases; semi-supervised learning method; K-means cluster; information of proximal PTMs; two-step feature selection

Funding

  1. National Natural Science Foundation of China [61403077]
  2. Fundamental Research Fundations for the Central Universities [2412019 FZ047, 2412019FZ048]
  3. Fundamental Research Funds for the Central Universities [3132020221]

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Protein succinylation is a key post-translational modification that plays a role in protein conformation regulation and cellular function control. This study proposes a new semi-supervised learning method, SSKM_Succ, to identify reliable non-succinylation lysine sites as negative samples. The method utilizes clustering, feature selection, and support vector machine to construct prediction models for succinylation sites with promising results. The study also suggests potential connections between succinylated protein and amino acid degradation, fatty acid metabolism, and neurodegenerative diseases.
Protein succinylation is a type of post-translational modification (PTM) that occurs on lysine sites and plays a key role in protein conformation regulation and cellular function control. When training in computational method, it is difficult to designate negative samples because of the uncertainty of non-succinylation lysine sites, and if not handled properly, it may affect the performance of computational models dramatically. Therefore, we propose a new semi-supervised learning method to identify reliable non-succinylation lysine sites as negative samples. This method, named SSKM_Succ, also employs K-means clustering to divide data into 5 clusters. Besides, information of proximal PTMs and three kinds of sequence features (grey pseudo amino acid composition, K-space and position-special amino acid propensity) are utilized to formulate protein. Then, we perform a two-step feature selection to remove redundant features and construct the optimization model for each cluster. Finally, support vector machine is applied to construct a prediction model for each cluster. Promising results are obtained by this method with an accuracy of 80.18 percent for succinylation sites on the independent testing dataset. Meanwhile, we compare the result with other existing tools, and it shows that our method is promising for predicting succinylation sites. Through analysis, we further verify that succinylated protein has potential effects on amino acid degradation and fatty acid metabolism, and speculate that protein succinylation may be closely related to neurodegenerative diseases.

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