Evidence map›Paper›PMID 40211147›Full record

ArticleBMC genomics2025

Protein structural domain-disease association prediction based on heterogeneous networks.

Jingpu Zhang, Lianping Deng, Lei Deng

Abstract read
In one paragraph

Article in BMC genomics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jingpu ZhangSchool of Computer and Data Science, Henan University of Urban Construction, 467000, Pingdingshan, China.ORCID http://orcid.org/0000-0002-8006-747X
Lianping DengSchool of Computer Science and Engineering, Central South University, 410075, Changsha, China.
Lei DengSchool of Computer Science and Engineering, Central South University, 410075, Changsha, China. leideng@csu.edu.cn.

Funding

National Natural Science Foundation of China 62172140
6 · The paper itself

Abstract

backgroundDomains can be viewed as portable units of protein structure, folding, function, evolution, and design. Small proteins are often found to be composed of only a single domain, while most large proteins consist of multiple domains for achieving various composite cellular functions. A dysfunction in domains may affect the function of proteins in some disease. Inferring the disease-related domains will help our understanding of the mechanism of human complex diseases.

resultsIn this study, we firstly build a global heterogeneous information network based on structural-based domains, proteins, and diseases. Then the topological features of the network are extracted according to the meta-paths between domain and disease nodes. Finally, we train a binary classifier based on the XGBOOST (eXtreme Gradient Boosting) algorithm to predict the potential associations between domains and diseases. The results show that the binary classification model using the XGBOOST algorithm performs significantly better than models using other machine learning algorithms, achieving an AUC (Area Under Curve) score of 0.94 in the leave-one-out cross-validation experiment.

conclusionsWe develop a method to build a binary classifier using the topological features based on meta-paths and predict the potential associations between domains and diseases. Based on its predictive performance in independent test sets, the method is proved to be powerful. Moreover, representing domains and diseases through integrating more multi-omic data will further optimize predictive performance.

Indexed as

Computational BiologyDiseaseProtein DomainsProteinsAlgorithmsHumansMachine LearningProteinsDomain-disease association predictionHeterogeneous networksMeta-path topological feature

Identifiers

PMID40211147
PMCPMC11987217

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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.