Evidence map›Paper›PMID 36246655›Full record

ArticleFrontiers in genetics2022

Deep_KsuccSite: A novel deep learning method for the identification of lysine succinylation sites.

Xin Liu, Lin-Lin Xu, Ya-Ping Lu, Ting Yang, Xin-Yu Gu, Liang Wang, Yong Liu

Abstract read
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Article in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

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0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Xin LiuSchool of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, China.
Lin-Lin XuSchool of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, China.
Ya-Ping LuCollege of Computer Science and Technology, China University of Mining and Technology, Xuzhou, China.
Ting YangSchool of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, China.
Xin-Yu GuSchool of Medical Informatics and Engineering, Xuzhou Medical University, Xuzhou, China.
Liang WangLaboratory Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Yong LiuJiangsu Center for the Collaboration and Innovation of Cancer Biotherapy, Cancer Institute, Xuzhou Medical University, Xuzhou, Jiangsu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Identification of lysine (symbol Lys or K) succinylation (Ksucc) sites centralizes the basis for disclosing the mechanism and function of lysine succinylation modifications. Traditional experimental methods for Ksucc site ientification are often costly and time-consuming. Therefore, it is necessary to construct an efficient computational method to prediction the presence of Ksucc sites in protein sequences. In this study, we proposed a novel and effective predictor for the identification of Ksucc sites based on deep learning algorithms that was termed as Deep_KsuccSite. The predictor adopted Composition, Transition, and Distribution (CTD) Composition (CTDC), Enhanced Grouped Amino Acid Composition (EGAAC), Amphiphilic Pseudo-Amino Acid Composition (APAAC), and Embedding Encoding methods to encode peptides, then constructed three base classifiers using one-dimensional (1D) convolutional neural network (CNN) and 2D-CNN, and finally utilized voting method to get the final results. K-fold cross-validation and independent testing showed that Deep_KsuccSite could serve as an effective tool to identify Ksucc sites in protein sequences. In addition, the ablation experiment results based on voting, feature combination, and model architecture showed that Deep_KsuccSite could make full use of the information of different features to construct an effective classifier. Taken together, we developed Deep_KsuccSite in this study, which was based on deep learning algorithm and could achieved better prediction accuracy than current methods for lysine succinylation sites. The code and dataset involved in this methodological study are permanently available at the URL https://github.com/flyinsky6/Deep_KsuccSite.

Indexed as

CNNdeep learninglysine succinylationpost-translational modificationprotein

Identifiers

PMID36246655
PMCPMC9557156

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.