SynSysNet: integration of experimental data on synaptic protein-protein interactions with drug-target relations

被引:33
|
作者
von Eichborn, Joachim [1 ]
Dunkel, Mathias [1 ]
Gohlke, Bjoern O. [1 ]
Preissner, Sarah C. [1 ]
Hoffmann, Michael F. [1 ]
Bauer, Jakob M. J. [1 ]
Armstrong, J. D. [2 ]
Schaefer, Martin H. [3 ]
Andrade-Navarro, Miguel A. [3 ]
Le Novere, Nicolas [4 ]
Croning, Michael D. R. [5 ,6 ]
Grant, Seth G. N. [5 ,6 ]
van Nierop, Pim [7 ]
Smit, August B. [7 ]
Preissner, Robert [1 ]
机构
[1] Charite, Inst Physiol, Struct Bioinformat Grp, D-13125 Berlin, Germany
[2] Sch Informat, Inst Neural Computat, Edinburgh EH8 9AB, Midlothian, Scotland
[3] Max Delbruck Ctr Mol Med, Computat Biol Grp, D-13125 Berlin, Germany
[4] Babraham Inst, Cambridge CB22 3AT, England
[5] Univ Edinburgh, Ctr Clin Brain Sci, Genes Cognit Programme, Edinburgh EH16 4SB, Midlothian, Scotland
[6] Univ Edinburgh, Ctr Neuroregenerat, Edinburgh EH16 4SB, Midlothian, Scotland
[7] Vrije Univ Amsterdam, Ctr Neurogen, Dept Mol & Cellular Neurobiol, NL-1081 HV Amsterdam, Netherlands
基金
英国生物技术与生命科学研究理事会;
关键词
DISEASES;
D O I
10.1093/nar/gks1040
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We created SynSysNet, available online at http://bioinformatics.charite.de/synsysnet, to provide a platform that creates a comprehensive 4D network of synaptic interactions. Neuronal synapses are fundamental structures linking nerve cells in the brain and they are responsible for neuronal communication and information processing. These processes are dynamically regulated by a network of proteins. New developments in interaction proteomics and yeast two-hybrid methods allow unbiased detection of interactors. The consolidation of data from different resources and methods is important to understand the relation to human behaviour and disease and to identify new therapeutic approaches. To this end, we established SynSysNet from a set of similar to 1000 synapse specific proteins, their structures and small-molecule interactions. For two-thirds of these, 3D structures are provided (from Protein Data Bank and homology modelling). Drug-target interactions for 750 approved drugs and 50 000 compounds, as well as 5000 experimentally validated protein-protein interactions, are included. The resulting interaction network and user-selected parts can be viewed interactively and exported in XGMML. Approximately 200 involved pathways can be explored regarding drug-target interactions. Homology-modelled structures are downloadable in Protein Data Bank format, and drugs are available as MOL-files. Protein-protein interactions and drug-target interactions can be viewed as networks; corresponding PubMed IDs or sources are given.
引用
收藏
页码:D834 / D840
页数:7
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