Evidence map›Paper›PMID 37740312›Full record

ArticleBioinformatics (Oxford, England)2023

Unbiased curriculum learning enhanced global-local graph neural network for protein thermodynamic stability prediction.

Haifan Gong, Yumeng Zhang, Chenhe Dong, Yue Wang, Guanqi Chen, Bilin Liang, Haofeng Li, Lanxuan Liu, Jie Xu, Guanbin Li

Open access · goldAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
2.6field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 17 citations in OpenAlex.

  1. De Novo Multi-Mechanism Antimicrobial Peptide Design via Multimodal Deep Learning.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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4 · The record

Corrections and comments

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

10 authors at 5 institutions in 1 country.

Haifan GongShanghai Artificial Intelligence Laboratory, Shanghai 200000, China.ORCID 0000-0002-2749-6830
Yumeng ZhangShanghai Jiao Tong University, Shanghai 200000, China.ORCID 0000-0002-6444-292X
Chenhe DongSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou 510000, China.ORCID 0000-0002-2211-5138
Yue WangQilu Hospital, Shandong University, Shandong 250000, China.ORCID 0000-0003-2486-6071
Guanqi ChenSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou 510000, China.ORCID 0000-0002-1440-3340
Bilin LiangShanghai Artificial Intelligence Laboratory, Shanghai 200000, China.
Haofeng LiSRIBD, Chinese University of Hong Kong (Shenzhen), Shenzhen 518000, China.ORCID 0000-0001-9120-9843
Lanxuan LiuShanghai Artificial Intelligence Laboratory, Shanghai 200000, China.
Jie XuShanghai Artificial Intelligence Laboratory, Shanghai 200000, China.ORCID 0000-0001-9233-4363
Guanbin LiSchool of Computer Science and Engineering, Sun Yat-sen University, Guangzhou 510000, China.ORCID 0000-0002-4805-0926
Sun Yat-sen University · CNBeijing Academy of Artificial Intelligence · CNQilu Hospital of Shandong University · CNShanghai Jiao Tong University · CNShenzhen Research Institute of Big Data · CN

Funding

Guangdong Basic and Applied Basic Research Foundation 2020B1515020048National Natural Science Foundation of China 62322608Shanghai Artificial Intelligence Laboratory
6 · The paper itself

Abstract

motivationProteins play crucial roles in biological processes, with their functions being closely tied to thermodynamic stability. However, measuring stability changes upon point mutations of amino acid residues using physical methods can be time-consuming. In recent years, several computational methods for protein thermodynamic stability prediction (PTSP) based on deep learning have emerged. Nevertheless, these approaches either overlook the natural topology of protein structures or neglect the inherent noisy samples resulting from theoretical calculation or experimental errors.

resultsWe propose a novel Global-Local Graph Neural Network powered by Unbiased Curriculum Learning for the PTSP task. Our method first builds a Siamese graph neural network to extract protein features before and after mutation. Since the graph's topological changes stem from local node mutations, we design a local feature transformation module to make the model focus on the mutated site. To address model bias caused by noisy samples, which represent unavoidable errors from physical experiments, we introduce an unbiased curriculum learning method. This approach effectively identifies and re-weights noisy samples during the training process. Extensive experiments demonstrate that our proposed method outperforms advanced protein stability prediction methods, and surpasses state-of-the-art learning methods for regression prediction tasks. AVAILABILITY AND IMPLEMENTATION: All code and data is available at https://github.com/haifangong/UCL-GLGNN.

Indexed as

Amino AcidsCurriculumNeural Networks, ComputerProtein StabilityThermodynamicsAmino Acids

Identifiers

PMID37740312
PMCPMC10918760
OpenAlexW4386979563

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.