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dc.contributor.author Fazekas D,
dc.contributor.author Koltai M,
dc.contributor.author Türei, Dénes
dc.contributor.author Módos, Dezső
dc.contributor.author Palfy M,
dc.contributor.author Dúl, Zoltán
dc.contributor.author Zsákai, Lilian
dc.contributor.author Földvári-Nagy Lászlóné Lenti, Katalin
dc.contributor.author Farkas, Illés
dc.contributor.author Vellai, Tibor
dc.contributor.author Csermely, Péter
dc.contributor.author Korcsmáros, Tamás
dc.date.accessioned 2015-02-25T11:23:01Z
dc.date.available 2015-02-25T11:23:01Z
dc.date.issued 2013
dc.identifier 84872321385
dc.identifier.citation pagination=7; journalVolume=7; journalTitle=BMC SYSTEMS BIOLOGY;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/984
dc.identifier.uri doi:10.1186/1752-0509-7-7
dc.description.abstract ABSTRACT: BACKGROUND: Signaling networks in eukaryotes are made up of upstream and downstream subnetworks. The upstream subnetwork contains the intertwined network of signaling pathways, while the downstream regulatory part contains transcription factors and their binding sites on the DNA as well as microRNAs and their mRNA targets. Currently, most signaling and regulatory databases contain only a subsection of this network, making comprehensive analyses highly time-consuming and dependent on specific data handling expertise. The need for detailed mapping of signaling systems is also supported by the fact that several drug development failures were caused by undiscovered cross-talk or regulatory effects of drug targets. We previously created a uniformly curated signaling pathway resource, SignaLink, to facilitate the analysis of pathway cross-talks. Here, we present SignaLink 2, which significantly extends the coverage and applications of its predecessor.Description: We developed a novel concept to integrate and utilize different subsections (i.e., layers) of the signaling network. The multi-layered (onion-like) database structure is made up of signaling pathways, their pathway regulators (e.g., scaffold and endocytotic proteins) and modifier enzymes (e.g., phosphatases, ubiquitin ligases), as well as transcriptional and post-transcriptional regulators of all of these components. The user-friendly website allows the interactive exploration of how each signaling protein is regulated. The customizable download page enables the analysis of any user-specified part of the signaling network. Compared to other signaling resources, distinctive features of SignaLink 2 are the following: 1) it involves experimental data not only from humans but from two invertebrate model organisms, C. elegans and D. melanogaster; 2) combines manual curation with large-scale datasets; 3) provides confidence scores for each interaction; 4) operates a customizable download page with multiple file formats (e.g., BioPAX, Cytoscape, SBML). Non-profit users can access SignaLink 2 free of charge at http://SignaLink.org CONCLUSIONS: With SignaLink 2 as a single resource, users can effectively analyze signaling pathways, scaffold proteins, modifier enzymes, transcription factors and miRNAs that are important in the regulation of signaling processes. This integrated resource allows the systems-level examination of how cross-talks and signaling flow are regulated, as well as provide data for cross-species comparisons and drug discovery analyses.
dc.relation.ispartof urn:issn:1752-0509
dc.title SignaLink 2 - a signaling pathway resource with multi-layered regulatory networks
dc.type Journal Article
dc.date.updated 2015-01-08T13:00:52Z
dc.language.rfc3066 en
dc.identifier.mtmt 2177153
dc.identifier.wos 000316274300001
dc.identifier.pubmed 23331499
dc.contributor.department ELTE/ELTE TTK/ELTE TTK Fizikai Intézet
dc.contributor.department ELTE/ELTE TTK/ELTE TTK Biológiai Intézet
dc.contributor.department SE/AOK/I/Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet
dc.contributor.department SE/ETK/AEI/Morfológiai és Fiziológiai Tanszék
dc.contributor.institution Eötvös Loránd Tudományegyetem
dc.contributor.institution Semmelweis Egyetem


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