{"title":"AIUPred - Binding: Energy Embedding to Identify Disordered Binding Regions.","authors":"Gábor Erdős, Norbert Deutsch, Zsuzsanna Dosztányi","doi":"10.1016/j.jmb.2025.169071","DOIUrl":null,"url":null,"abstract":"<p><p>Intrinsically disordered regions (IDRs) play critical roles in various cellular processes, often mediating interactions through disordered binding regions that transition to ordered states. Experimental characterization of these functional regions is highly challenging, underscoring the need for fast and accurate computational tools. Despite their importance, predicting disordered binding regions remains a significant challenge due to limitations in existing datasets and methodologies. In this study, we introduce AIUPred-binding, a novel prediction tool leveraging a high dimensional mathematical representation of structural energies - we call energy embedding - and pathogenicity scores from AlphaMissense. By employing a transfer learning approach, AIUPred-binding demonstrates improved accuracy in identifying functional sites within IDRs. Our results highlight the tool's ability to discern subtle features within disordered regions, addressing biases and other challenges associated with manually curated datasets. We present AIUPred-binding integrated into the AIUPred web framework as a versatile and efficient resource for understanding the functional roles of IDRs. AIUPred-binding is freely accessible at https://aiupred.elte.hu.</p>","PeriodicalId":369,"journal":{"name":"Journal of Molecular Biology","volume":" ","pages":"169071"},"PeriodicalIF":4.7000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.jmb.2025.169071","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Intrinsically disordered regions (IDRs) play critical roles in various cellular processes, often mediating interactions through disordered binding regions that transition to ordered states. Experimental characterization of these functional regions is highly challenging, underscoring the need for fast and accurate computational tools. Despite their importance, predicting disordered binding regions remains a significant challenge due to limitations in existing datasets and methodologies. In this study, we introduce AIUPred-binding, a novel prediction tool leveraging a high dimensional mathematical representation of structural energies - we call energy embedding - and pathogenicity scores from AlphaMissense. By employing a transfer learning approach, AIUPred-binding demonstrates improved accuracy in identifying functional sites within IDRs. Our results highlight the tool's ability to discern subtle features within disordered regions, addressing biases and other challenges associated with manually curated datasets. We present AIUPred-binding integrated into the AIUPred web framework as a versatile and efficient resource for understanding the functional roles of IDRs. AIUPred-binding is freely accessible at https://aiupred.elte.hu.
期刊介绍:
Journal of Molecular Biology (JMB) provides high quality, comprehensive and broad coverage in all areas of molecular biology. The journal publishes original scientific research papers that provide mechanistic and functional insights and report a significant advance to the field. The journal encourages the submission of multidisciplinary studies that use complementary experimental and computational approaches to address challenging biological questions.
Research areas include but are not limited to: Biomolecular interactions, signaling networks, systems biology; Cell cycle, cell growth, cell differentiation; Cell death, autophagy; Cell signaling and regulation; Chemical biology; Computational biology, in combination with experimental studies; DNA replication, repair, and recombination; Development, regenerative biology, mechanistic and functional studies of stem cells; Epigenetics, chromatin structure and function; Gene expression; Membrane processes, cell surface proteins and cell-cell interactions; Methodological advances, both experimental and theoretical, including databases; Microbiology, virology, and interactions with the host or environment; Microbiota mechanistic and functional studies; Nuclear organization; Post-translational modifications, proteomics; Processing and function of biologically important macromolecules and complexes; Molecular basis of disease; RNA processing, structure and functions of non-coding RNAs, transcription; Sorting, spatiotemporal organization, trafficking; Structural biology; Synthetic biology; Translation, protein folding, chaperones, protein degradation and quality control.