Evidence map›Paper›PMID 38972994›Full record

ArticleJournal of cheminformatics2024

LVPocket: integrated 3D global-local information to protein binding pockets prediction with transfer learning of protein structure classification.

Ruifeng Zhou, Jing Fan, Sishu Li, Wenjie Zeng, Yilun Chen, Xiaoshan Zheng, Hongyang Chen, Jun Liao

Abstract read
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Article in Journal of cheminformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Can Cavity Prediction Algorithms Help in Docking Experiments?Journal of computational chemistry · 2026
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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Ruifeng ZhouSchool of Science, China Pharmaceutical University, Nanjing, 210009, Jiangsu, People's Republic of China.
Jing FanSchool of Science, China Pharmaceutical University, Nanjing, 210009, Jiangsu, People's Republic of China.
Sishu LiSchool of Science, China Pharmaceutical University, Nanjing, 210009, Jiangsu, People's Republic of China.
Wenjie ZengSchool of Science, China Pharmaceutical University, Nanjing, 210009, Jiangsu, People's Republic of China.
Yilun ChenSchool of Science, China Pharmaceutical University, Nanjing, 210009, Jiangsu, People's Republic of China.
Xiaoshan ZhengSchool of Science, China Pharmaceutical University, Nanjing, 210009, Jiangsu, People's Republic of China.
Hongyang ChenResearch Center for Graph Computing, Zhejiang Lab, Hangzhou, 311121, Zhejiang, People's Republic of China. hongyang@zhejianglab.com.ORCID http://orcid.org/0000-0002-7626-0162
Jun LiaoSchool of Science, China Pharmaceutical University, Nanjing, 210009, Jiangsu, People's Republic of China. liaojun@cpu.edu.cn.ORCID http://orcid.org/0000-0003-0617-5840

Funding

Ab initio design and generation of AI models for small molecule ligands based on target structures 2022PE0AC03A study on the diagnosis of addiction to synthetic cannabinoids and methods of assessing the risk of abuse 2022YFC3300905The research on key technologies for monitoring and identifying drug abuse of anesthetic drugs and psychotropic drugs, and intervention for addiction 2023YFC3304200
6 · The paper itself

Abstract

backgroundPrevious deep learning methods for predicting protein binding pockets mainly employed 3D convolution, yet an abundance of convolution operations may lead the model to excessively prioritize local information, thus overlooking global information. Moreover, it is essential for us to account for the influence of diverse protein folding structural classes. Because proteins classified differently structurally exhibit varying biological functions, whereas those within the same structural class share similar functional attributes.

resultsWe proposed LVPocket, a novel method that synergistically captures both local and global information of protein structure through the integration of Transformer encoders, which help the model achieve better performance in binding pockets prediction. And then we tailored prediction models for data of four distinct structural classes of proteins using the transfer learning. The four fine-tuned models were trained on the baseline LVPocket model which was trained on the sc-PDB dataset. LVPocket exhibits superior performance on three independent datasets compared to current state-of-the-art methods. Additionally, the fine-tuned model outperforms the baseline model in terms of performance. SCIENTIFIC CONTRIBUTION: We present a novel model structure for predicting protein binding pockets that provides a solution for relying on extensive convolutional computation while neglecting global information about protein structures. Furthermore, we tackle the impact of different protein folding structures on binding pocket prediction tasks through the application of transfer learning methods.

Indexed as

Protein binding pockets predictionProtein structural classificationTransfer learningTransformer encoder

Identifiers

PMID38972994
PMCPMC11229186

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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.