A computational tool to infer enzyme activity using post-translational modification profiling data

Abstract Enzymes play a pivotal role in orchestrating complex cellular responses to external stimuli and environmental changes through signal transduction pathways. Despite their crucial roles, measuring enzyme activities is typically indirect and performed on a smaller scale, unlike protein abundan...

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Main Authors: Dehui Kong, Aijun Zhang, Ling Li, Zuo-Fei Yuan, Yingxue Fu, Long Wu, Ashutosh Mishra, Anthony A. High, Junmin Peng, Xusheng Wang
Format: Article
Language:English
Published: Nature Portfolio 2025-01-01
Series:Communications Biology
Online Access:https://doi.org/10.1038/s42003-025-07548-4
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author Dehui Kong
Aijun Zhang
Ling Li
Zuo-Fei Yuan
Yingxue Fu
Long Wu
Ashutosh Mishra
Anthony A. High
Junmin Peng
Xusheng Wang
author_facet Dehui Kong
Aijun Zhang
Ling Li
Zuo-Fei Yuan
Yingxue Fu
Long Wu
Ashutosh Mishra
Anthony A. High
Junmin Peng
Xusheng Wang
author_sort Dehui Kong
collection DOAJ
description Abstract Enzymes play a pivotal role in orchestrating complex cellular responses to external stimuli and environmental changes through signal transduction pathways. Despite their crucial roles, measuring enzyme activities is typically indirect and performed on a smaller scale, unlike protein abundance measured by high-throughput proteomics. Moreover, it is challenging to derive the activity of enzymes from proteome-wide post-translational modification (PTM) profiling data. To address this challenge, we introduce enzyme activity inference with structural equation modeling under the JUMP umbrella (JUMPsem), a novel computational tool designed to infer enzyme activity using PTM profiling data. We demonstrate that the JUMPsem program enables estimating kinase activities using phosphoproteome data, ubiquitin E3 ligase activities from the ubiquitinome, and histone acetyltransferase (HAT) activities based on the acetylome. In addition, JUMPsem is capable of establishing novel enzyme-substrate relationships through searching motif sequences. JUMPsem outperforms widely used kinase activity tools, such as IKAP and KSEA, in terms of the number of kinases and the computational speed. The JUMPsem program is scalable and publicly available as an open-source R package and user-friendly web-based R/Shiny app. Collectively, JUMPsem provides an improved tool for inferring protein enzyme activities, potentially facilitating targeted drug development.
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institution Kabale University
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spelling doaj-art-bcee18af6025428796dc249b3dbe544d2025-01-26T12:48:08ZengNature PortfolioCommunications Biology2399-36422025-01-01811810.1038/s42003-025-07548-4A computational tool to infer enzyme activity using post-translational modification profiling dataDehui Kong0Aijun Zhang1Ling Li2Zuo-Fei Yuan3Yingxue Fu4Long Wu5Ashutosh Mishra6Anthony A. High7Junmin Peng8Xusheng Wang9Department of Genetics, Genomics and Informatics, University of Tennessee Health Science CenterDepartment of Genetics, Genomics and Informatics, University of Tennessee Health Science CenterDepartment of Genetics, Genomics and Informatics, University of Tennessee Health Science CenterCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalCenter for Proteomics and Metabolomics, St. Jude Children’s Research HospitalDepartment of Structural Biology, St. Jude Children’s Research HospitalDepartment of Genetics, Genomics and Informatics, University of Tennessee Health Science CenterAbstract Enzymes play a pivotal role in orchestrating complex cellular responses to external stimuli and environmental changes through signal transduction pathways. Despite their crucial roles, measuring enzyme activities is typically indirect and performed on a smaller scale, unlike protein abundance measured by high-throughput proteomics. Moreover, it is challenging to derive the activity of enzymes from proteome-wide post-translational modification (PTM) profiling data. To address this challenge, we introduce enzyme activity inference with structural equation modeling under the JUMP umbrella (JUMPsem), a novel computational tool designed to infer enzyme activity using PTM profiling data. We demonstrate that the JUMPsem program enables estimating kinase activities using phosphoproteome data, ubiquitin E3 ligase activities from the ubiquitinome, and histone acetyltransferase (HAT) activities based on the acetylome. In addition, JUMPsem is capable of establishing novel enzyme-substrate relationships through searching motif sequences. JUMPsem outperforms widely used kinase activity tools, such as IKAP and KSEA, in terms of the number of kinases and the computational speed. The JUMPsem program is scalable and publicly available as an open-source R package and user-friendly web-based R/Shiny app. Collectively, JUMPsem provides an improved tool for inferring protein enzyme activities, potentially facilitating targeted drug development.https://doi.org/10.1038/s42003-025-07548-4
spellingShingle Dehui Kong
Aijun Zhang
Ling Li
Zuo-Fei Yuan
Yingxue Fu
Long Wu
Ashutosh Mishra
Anthony A. High
Junmin Peng
Xusheng Wang
A computational tool to infer enzyme activity using post-translational modification profiling data
Communications Biology
title A computational tool to infer enzyme activity using post-translational modification profiling data
title_full A computational tool to infer enzyme activity using post-translational modification profiling data
title_fullStr A computational tool to infer enzyme activity using post-translational modification profiling data
title_full_unstemmed A computational tool to infer enzyme activity using post-translational modification profiling data
title_short A computational tool to infer enzyme activity using post-translational modification profiling data
title_sort computational tool to infer enzyme activity using post translational modification profiling data
url https://doi.org/10.1038/s42003-025-07548-4
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