
doi: 10.1101/609149 , 10.1109/bibm.2018.8621571 , 10.1186/s12859-019-3077-x , 10.60692/xntaq-mgf29 , 10.60692/e4j9x-20w07 , 10.60692/xkvay-rf977 , 10.60692/1ysb3-7q432
pmid: 31787091
pmc: PMC6886211
handle: 10919/95991
doi: 10.1101/609149 , 10.1109/bibm.2018.8621571 , 10.1186/s12859-019-3077-x , 10.60692/xntaq-mgf29 , 10.60692/e4j9x-20w07 , 10.60692/xkvay-rf977 , 10.60692/1ysb3-7q432
pmid: 31787091
pmc: PMC6886211
handle: 10919/95991
AbstractUnderstanding cellular responses via signal transduction is a core focus in systems biology. Tools to automatically reconstruct signaling pathways from protein-protein interactions (PPIs) can help biologists generate testable hypotheses about signaling. However, automatic reconstruction of signaling pathways suffers from many interactions with the same confidence score leading to many equally good candidates. Further, some reconstructions are biologically misleading due to ignoring protein localization information. We proposeLocPL, a method to improve the automatic reconstruction of signaling pathways from PPIs by incorporating information about protein localization in the reconstructions. The method relies on a dynamic program to ensure that the proteins in a reconstruction are localized in cellular compartments that are consistent with signal transduction from the membrane to the nucleus.LocPLand existing reconstruction algorithms are applied to two PPI networks and assessed using both global and local definitions of accuracy.LocPLproduces more accurate and biologically meaningful reconstructions on a versatile set of signaling pathways.LocPLis a powerful tool to automatically reconstruct signaling pathways from PPIs that leverages cellular localization information about proteins. The underlying dynamic program and signaling model are flexible enough to study cellular signaling under different settings of signaling flow across the cellular compartments.
FOS: Computer and information sciences, Cell signaling, Artificial intelligence, Signaling pathways, Interactome, Protein-Protein Interaction Networks, Signal transduction, Gene, Computational biology, Automation, Protein-protein interaction, Protein Interaction Mapping, Biology (General), Biological pathway, Biological networks, Physics, Life Sciences, Focus (optics), Analysis of Gene Interaction Networks, Programming language, Stochasticity in Gene Regulatory Networks, Protein Transport, Medicine, Algorithms, Protein Binding, Signal Transduction, Cell biology, QH301-705.5, Bioinformatics, Computer applications to medicine. Medical informatics, R858-859.7, Pathway Analysis, Set (abstract data type), Biochemistry, Genetics and Molecular Biology, Health Sciences, Genetics, Humans, Molecular Biology, Biology, Pharmacology, Signaling proteins, Protein Structure Prediction and Analysis, Protein localization, Research, Metabolic Engineering and Synthetic Biology, Computational Biology, Proteins, Natural Products as Sources of New Drugs, Optics, Computer science, Biological Network Integration, FOS: Biological sciences, Gene expression
FOS: Computer and information sciences, Cell signaling, Artificial intelligence, Signaling pathways, Interactome, Protein-Protein Interaction Networks, Signal transduction, Gene, Computational biology, Automation, Protein-protein interaction, Protein Interaction Mapping, Biology (General), Biological pathway, Biological networks, Physics, Life Sciences, Focus (optics), Analysis of Gene Interaction Networks, Programming language, Stochasticity in Gene Regulatory Networks, Protein Transport, Medicine, Algorithms, Protein Binding, Signal Transduction, Cell biology, QH301-705.5, Bioinformatics, Computer applications to medicine. Medical informatics, R858-859.7, Pathway Analysis, Set (abstract data type), Biochemistry, Genetics and Molecular Biology, Health Sciences, Genetics, Humans, Molecular Biology, Biology, Pharmacology, Signaling proteins, Protein Structure Prediction and Analysis, Protein localization, Research, Metabolic Engineering and Synthetic Biology, Computational Biology, Proteins, Natural Products as Sources of New Drugs, Optics, Computer science, Biological Network Integration, FOS: Biological sciences, Gene expression
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