Nucleic Acids Research Advance Access originally published online on November 10, 2006
Nucleic Acids Research 2007 35(Database issue):D358-D362; doi:10.1093/nar/gkl825
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Nucleic Acids Research, 2007, Vol. 35, Database issue D358-D362
© 2006 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
Articles |
STRING 7recent developments in the integration and prediction of protein interactions
1 European Molecular Biology Laboratory, Meyerhofstrasse 1 69117 Heidelberg, Germany 2 University of Zurich, Winterthurerstrasse 190 8057 Zurich, Switzerland 3 Utrecht University, Padualaan 8 3584 CH Utrecht, The Netherlands 4 Max-Delbrück-Centre for Molecular Medicine, Robert-Rössle-Str. 10 13092 Berlin, Germany
*To whom correspondence should be addressed. Tel: +41 44 6353147; Fax: +41 44 6356864; Email: mering{at}molbio.unizh.ch
Received September 15, 2006. Revised October 5, 2006. Accepted October 5, 2006.
| ABSTRACT |
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Information on proteinprotein interactions is still mostly limited to a small number of model organisms, and originates from a wide variety of experimental and computational techniques. The database and online resource STRING generalizes access to protein interaction data, by integrating known and predicted interactions from a variety of sources. The underlying infrastructure includes a consistent body of completely sequenced genomes and exhaustive orthology classifications, based on which interaction evidence is transferred between organisms. Although primarily developed for protein interaction analysis, the resource has also been successfully applied to comparative genomics, phylogenetics and network studies, which are all facilitated by programmatic access to the database backend and the availability of compact download files. As of release 7, STRING has almost doubled to 373 distinct organisms, and contains more than 1.5 million proteins for which associations have been pre-computed. Novel features include AJAX-based web-navigation, inclusion of additional resources such as BioGRID, and detailed protein domain annotation. STRING is available at http://string.embl.de/
| INTRODUCTION |
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A fully comprehensive view of all functionally relevant protein interactions is still not available for any species, not even for relatively simple, single-celled model organisms. However, this information is essential for a systems-level understanding of cellular behavior, and it is needed in order to place the molecular functions of individual proteins into their cellular context.
For detecting direct physical binding between proteins, numerous small-scale and high-throughput experiments have been undertaken, and most of their reported interactions are available from dedicated interaction databases (14), as well as from multipurpose databases centered on specific model organisms (57). However, the growth of interaction data is severely lagging behind the pace of genome sequencing, so that for most genomes and proteins known to date no interaction data is available. Furthermore, proteins do not only interact physically: indirect associations such as genetic interactions or shared pathway memberships are equally important for a complete understanding of cellular function, but are for the most part not stored in interaction databases. Instead, they are available from a variety of pathway databases (8,9) and from the scientific literature.
The database STRING (Search Tool for the Retrieval of Interacting Genes/Proteins) aims to collect, predict and unify most types of proteinprotein associations, including direct and indirect associations. In order to cover organisms not yet addressed experimentally, STRING runs a set of prediction algorithms (10), and transfers known interactions from model organisms to other species based on predicted orthology of the respective proteins (11). STRING has grown from a purely predictive resource covering mainly prokaryotes (12) to a comprehensive tool integrating protein association information from all domains of life (Figure 1). Each interaction in the database is annotated with a benchmarked numerical confidence score, which can be used to filter the interaction network at any desired stringency. All data in STRING are stored in relational database tables. The interaction information is freely available for download, but download of the entire database content requires a license agreement to prevent redistribution (free for academic users who only access the previous version number).
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| KNOWN AND PREDICTED INTERACTIONS |
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Known interactions in STRING are primarily imported from existing excellent interaction databases (15,8,9), and are complemented by automated text mining of PubMed abstracts and several other bodies of scientific text [such as from Ref. (6)]. As is the case for all interactions in STRING, imported interactions are mapped onto a consistent set of proteins and identifiers, thereby facilitating comparison between datasets. STRING does not store specific details regarding splicing isoforms or post-translational modifications, but instead reduces protein isoforms to a single protein per locus (usually as defined by the longest known protein-coding transcript). This level of resolution enables efficient storage and is compatible with most prediction/transfer algorithms, which usually operate only at the level of the gene locus.
Known interactions are further complemented by de novo interaction predictions derived from several comparative genomics prediction algorithms that are mainly applicable to prokaryotes (1319). These algorithms systematically compare genomes, searching for frequently observed gene neighborhoods, gene fusion events and similarities in gene occurrence across genomes. For each prediction algorithm, dedicated viewers of the genomic evidence are available in STRING.
Interaction evidence from model organisms is often useful for other organisms as well, especially when orthologs of interacting proteins can be clearly identified in the second organism. STRING systematically executes such orthology transfers, using both precomputed orthologs from the COG database (20), as well as a homology-based orthology scheme computed de novo (11). STRING can thus immediately predict a large number of interactions for any newly sequenced genome, as soon as it is included into the system. The combination of known, predicted and transferred interactions is unique, making STRING the most comprehensive interaction resource available to date, especially for organisms not addressed experimentally.
The homology data stored in STRING form the basis for the interaction transfers, and are the result of more than 7 x 1011 pairwise protein comparisons using the sensitive SmithWaterman dynamic programming algorithm. This dataset is a very useful asset in itself [see also (21)], and can be accessed independently of the protein interaction networks by locally installing the STRING database files. Users of the website can also browse all of the homologs detected for any protein of interest, and can inspect alignments with very fast response times (Figure 2).
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| NEW FEATURES AND IMPROVEMENTS IN STRING 7 |
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The network viewer in STRING (Figure 1) is the central information source and navigation hub for the user. It has been extended through a context-sensitive menu-box, which displays associated information for any protein in the network. This menu includes a graphical summary of protein domains and features, and allows the user to link out to other external resources such as the motif discovery tool DILIMOT (22). STRING is now also tightly integrated with the SMART protein architecture research tool (23). With the latter it shares a common set of genomes and proteins, for which consistent results are pre-computed and stored. This enables automatic interlinking between both resources (SMART includes interaction previews, and STRING includes domain architecture previews). The topology and evolution of interaction networks can thus be studied both at the level of proteins as well as at the level of individual domains.
Since the last update (11), STRING has grown substantially both in terms of data sources and number of organisms covered. Five new databases are included [MINT, HPRD, BioGRID, DIP and Reactome (25,8)], as well as 194 new organisms. Especially due to this latter increase in completely sequenced organisms, the architecture of STRING had to be substantially upgraded so that it can accommodate present and future growth. With respect to the user interface, this required changes in the viewers for the genomic context data, which could no longer show all of the genomes simultaneously by default. Instead, STRING uses a phylogenetic tree of species to collapse redundant genomes; this tree has been derived from concatenated alignments of a small number of universal protein families (24). Users can navigate the tree by expanding or collapsing its sub-branches, thus choosing which organisms to focus on. AJAX technology (Asynchronous JavaScript and XML) is then used to fetch the requested information into the existing, pre-loaded browser page, thus increasing useability and speed.
With respect to the underlying database structure, changes were necessary in the way homology data and interaction transfers are stored. Both can no longer be computed and stored in an all-against-all fashion, because of their quadratic scaling with the number of genomes. Beginning with version 7, STRING therefore adopts a two-layered approach when accommodating fully sequenced genomes (Figure 3): important model organisms and those for which experimental data are available form the core genomes, all other genomes form the periphery. Within the core, homology searches and interaction transfers are still executed in an all-against-all fashion, whereas for peripheral genomes only searches against the core are included. These and other changes in STRING dramatically improve the scalability of the resource, leading to faster update cycles even when the number of sequenced genomes is to increase as fast as currently projected. Together with future plans to increase the scope and specificity of the stored interaction information, STRING should thus continue to facilitate not only network research but also wider projects that range from phylogenetics to metagenomics (24,25).
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| ACKNOWLEDGEMENTS |
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The authors wish to thank Dianna Fisk from the Saccharomyces Genome Database for access to the Gene Summary Paragraphs, and Toby Gibson, Martijn Huynen, Victor Neduva, Rune Linding and members of the Bork group for continued feedback and discussions. This work was supported in part by grants from the Bundesministerium für Forschung und Bildung, Germany, as well as through the ADIT Integrated Project, contract number LSHB-CT-2005-511065, and through the BioSapiens Network of Excellence, contract number LSHG-CT-2003-503265, both funded by the European Commission FP6 Programme. Funding to pay the Open Access publication charges for this article was provided by the University of Zurich, through its Research Priority Program Systems Biology and Functional Genomics.
Conflict of interest statement. None declared.
| Footnotes |
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The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors
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M.-E. Caruso, S. Jenna, M. Bouchecareilh, D. L. Baillie, D. Boismenu, D. Halawani, M. Latterich, and E. Chevet GTPase-Mediated Regulation of the Unfolded Protein Response in Caenorhabditis elegans Is Dependent on the AAA+ ATPase CDC-48 Mol. Cell. Biol., July 1, 2008; 28(13): 4261 - 4274. [Abstract] [Full Text] [PDF] |
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M. T. Dittrich, G. W. Klau, A. Rosenwald, T. Dandekar, and T. Muller Identifying functional modules in protein-protein interaction networks: an integrated exact approach Bioinformatics, July 1, 2008; 24(13): i223 - i231. [Abstract] [Full Text] [PDF] |
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J. Klein, S. Leupold, R. Munch, C. Pommerenke, T. Johl, U. Karst, L. Jansch, D. Jahn, and I. Retter ProdoNet: identification and visualization of prokaryotic gene regulatory and metabolic networks Nucleic Acids Res., July 1, 2008; 36(suppl_2): W460 - W464. [Abstract] [Full Text] [PDF] |
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B. E. Dutilh, Y. He, M. L. Hekkelman, and M. A. Huynen Signature, a web server for taxonomic characterization of sequence samples using signature genes Nucleic Acids Res., July 1, 2008; 36(suppl_2): W470 - W474. [Abstract] [Full Text] [PDF] |
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C.-Y. Lin, C.-H. Chin, H.-H. Wu, S.-H. Chen, C.-W. Ho, and M.-T. Ko Hubba: hub objects analyzer--a framework of interactome hubs identification for network biology Nucleic Acids Res., July 1, 2008; 36(suppl_2): W438 - W443. [Abstract] [Full Text] [PDF] |
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L.-C. Tranchevent, R. Barriot, S. Yu, S. Van Vooren, P. Van Loo, B. Coessens, B. De Moor, S. Aerts, and Y. Moreau ENDEAVOUR update: a web resource for gene prioritization in multiple species Nucleic Acids Res., July 1, 2008; 36(suppl_2): W377 - W384. [Abstract] [Full Text] [PDF] |
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C. E. Martinez-Guerrero, R. Ciria, C. Abreu-Goodger, G. Moreno-Hagelsieb, and E. Merino GeConT 2: gene context analysis for orthologous proteins, conserved domains and metabolic pathways Nucleic Acids Res., July 1, 2008; 36(suppl_2): W176 - W180. [Abstract] [Full Text] [PDF] |
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S. Brohee, K. Faust, G. Lima-Mendez, O. Sand, R. Janky, G. Vanderstocken, Y. Deville, and J. van Helden NeAT: a toolbox for the analysis of biological networks, clusters, classes and pathways Nucleic Acids Res., July 1, 2008; 36(suppl_2): W444 - W451. [Abstract] [Full Text] [PDF] |
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D. C. Teixeira, S. Eveillard, P. Sirand-Pugnet, A. Wulff, C. Saillard, A. J. Ayres, and J. M. Bove The tufB-secE-nusG-rplKAJL-rpoB gene cluster of the liberibacters: sequence comparisons, phylogeny and speciation Int J Syst Evol Microbiol, June 1, 2008; 58(6): 1414 - 1421. [Abstract] [Full Text] [PDF] |
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D. Li, W. Liu, Z. Liu, J. Wang, Q. Liu, Y. Zhu, and F. He PRINCESS, a Protein Interaction Confidence Evaluation System with Multiple Data Sources Mol. Cell. Proteomics, June 1, 2008; 7(6): 1043 - 1052. [Abstract] [Full Text] [PDF] |
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B. Lehner and I. Lee Network-guided genetic screening: building, testing and using gene networks to predict gene function Brief Funct Genomic Proteomic, May 1, 2008; 7(3): 217 - 227. [Abstract] [Full Text] [PDF] |
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Z. Mashhadi, H. Zhang, H. Xu, and R. H. White Identification and Characterization of an Archaeon-Specific Riboflavin Kinase J. Bacteriol., April 1, 2008; 190(7): 2615 - 2618. [Abstract] [Full Text] [PDF] |
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I. V. Tetko, I. V. Rodchenkov, M. C. Walter, T. Rattei, and H.-W. Mewes Beyond the 'best' match: machine learning annotation of protein sequences by integration of different sources of information Bioinformatics, March 1, 2008; 24(5): 621 - 628. [Abstract] [Full Text] [PDF] |
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P. R Kensche, V. van Noort, B. E Dutilh, and M. A Huynen Practical and theoretical advances in predicting the function of a protein by its phylogenetic distribution J R Soc Interface, February 6, 2008; 5(19): 151 - 170. [Abstract] [Full Text] [PDF] |
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B. W. Davies and G. C. Walker A Highly Conserved Protein of Unknown Function Is Required by Sinorhizobium meliloti for Symbiosis and Environmental Stress Protection J. Bacteriol., February 1, 2008; 190(3): 1118 - 1123. [Abstract] [Full Text] [PDF] |
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G. Moreno-Hagelsieb and K. Latimer Choosing BLAST options for better detection of orthologs as reciprocal best hits Bioinformatics, February 1, 2008; 24(3): 319 - 324. [Abstract] [Full Text] [PDF] |
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L. J. Jensen, P. Julien, M. Kuhn, C. von Mering, J. Muller, T. Doerks, and P. Bork eggNOG: automated construction and annotation of orthologous groups of genes Nucleic Acids Res., January 11, 2008; 36(suppl_1): D250 - D254. [Abstract] [Full Text] [PDF] |
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C. Su, J. M. Peregrin-Alvarez, G. Butland, S. Phanse, V. Fong, A. Emili, and J. Parkinson Bacteriome.org an integrated protein interaction database for E. coli Nucleic Acids Res., January 11, 2008; 36(suppl_1): D632 - D636. [Abstract] [Full Text] [PDF] |
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F. Diella, C. M. Gould, C. Chica, A. Via, and T. J. Gibson Phospho.ELM: a database of phosphorylation sites update 2008 Nucleic Acids Res., January 11, 2008; 36(suppl_1): D240 - D244. [Abstract] [Full Text] [PDF] |
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R. Linding, L. J. Jensen, A. Pasculescu, M. Olhovsky, K. Colwill, P. Bork, M. B. Yaffe, and T. Pawson NetworKIN: a resource for exploring cellular phosphorylation networks Nucleic Acids Res., January 11, 2008; 36(suppl_1): D695 - D699. [Abstract] [Full Text] [PDF] |
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P. Pagel, M. Oesterheld, O. Tovstukhina, N. Strack, V. Stumpflen, and D. Frishman DIMA 2.0 predicted and known domain interactions Nucleic Acids Res., January 11, 2008; 36(suppl_1): D651 - D655. [Abstract] [Full Text] [PDF] |
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M. Kuhn, C. von Mering, M. Campillos, L. J. Jensen, and P. Bork STITCH: interaction networks of chemicals and proteins Nucleic Acids Res., January 11, 2008; 36(suppl_1): D684 - D688. [Abstract] [Full Text] [PDF] |
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A.D.J. van Dijk, C.J.F. ter Braak, R.G. Immink, G.C. Angenent, and R.C.H.J. van Ham Predicting and understanding transcription factor interactions based on sequence level determinants of combinatorial control Bioinformatics, January 1, 2008; 24(1): 26 - 33. [Abstract] [Full Text] [PDF] |
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R. Varshavsky, A. Gottlieb, D. Horn, and M. Linial Unsupervised feature selection under perturbations: meeting the challenges of biological data Bioinformatics, December 15, 2007; 23(24): 3343 - 3349. [Abstract] [Full Text] [PDF] |
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J. Livny, Y. Yamaichi, and M. K. Waldor Distribution of Centromere-Like parS Sites in Bacteria: Insights from Comparative Genomics J. Bacteriol., December 1, 2007; 189(23): 8693 - 8703. [Abstract] [Full Text] [PDF] |
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B. S. Srinivasan, N. H. Shah, J. A. Flannick, E. Abeliuk, A. F. Novak, and S. Batzoglou Current progress in network research: toward reference networks for key model organisms Brief Bioinform, September 1, 2007; 8(5): 318 - 332. [Abstract] [Full Text] [PDF] |
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C. M. Arraiano, J. Bamford, H. Brussow, A. J. Carpousis, V. Pelicic, K. Pfluger, P. Polard, and J. Vogel Recent Advances in the Expression, Evolution, and Dynamics of Prokaryotic Genomes J. Bacteriol., September 1, 2007; 189(17): 6093 - 6100. [Full Text] [PDF] |
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R. W. Shultz, V. M. Tatineni, L. Hanley-Bowdoin, and W. F. Thompson Genome-Wide Analysis of the Core DNA Replication Machinery in the Higher Plants Arabidopsis and Rice Plant Physiology, August 1, 2007; 144(4): 1697 - 1714. [Abstract] [Full Text] [PDF] |
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C. Perez-Iratxeta, P. Bork, and M. A. Andrade-Navarro Update of the G2D tool for prioritization of gene candidates to inherited diseases Nucleic Acids Res., July 13, 2007; 35(suppl_2): W212 - W216. [Abstract] [Full Text] [PDF] |
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P. Smits, J. A. M. Smeitink, L. P. van den Heuvel, M. A. Huynen, and T. J. G. Ettema Reconstructing the evolution of the mitochondrial ribosomal proteome Nucleic Acids Res., July 9, 2007; 35(14): 4686 - 4703. [Abstract] [Full Text] [PDF] |
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G. Dawelbait, C. Winter, Y. Zhang, C. Pilarsky, R. Grutzmann, J.-C. Heinrich, and M. Schroeder Structural templates predict novel protein interactions and targets from pancreas tumour gene expression data Bioinformatics, July 1, 2007; 23(13): i115 - i124. [Abstract] [Full Text] [PDF] |
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