CLUSTERING-BASED APPROACH FOR PREDICTING MOTIF PAIRS FROM PROTEIN INTERACTION DATA

2009 ◽  
Vol 07 (04) ◽  
pp. 701-716 ◽  
Author(s):  
HENRY CHI-MING LEUNG ◽  
MAN-HUNG SIU ◽  
SIU-MING YIU ◽  
FRANCIS YUK-LUN CHIN ◽  
KEN WING-KIN SUNG

Predicting motif pairs from a set of protein sequences based on the protein–protein interaction data is an important, but difficult computational problem. Tan et al. proposed a solution to this problem. However, the scoring function (using χ2 testing) used in their approach is not adequate and their approach is also not scalable. It may take days to process a set of 5000 protein sequences with about 20,000 interactions. Later, Leung et al. proposed an improved scoring function and faster algorithms for solving the same problem. But, the model used in Leung et al. is complicated. The exact value of the scoring function is not easy to compute and an estimated value is used in practice. In this paper, we derive a better model to capture the significance of a given motif pair based on a clustering notion. We develop a fast heuristic algorithm to solve the problem. The algorithm is able to locate the correct motif pair in the yeast data set in about 45 minutes for 5000 protein sequences and 20,000 interactions. Moreover, we derive a lower bound result for the p-value of a motif pair in order for it to be distinguishable from random motif pairs. The lower bound result has been verified using simulated data sets. Availability:

2008 ◽  
Vol 7 (9) ◽  
pp. 3879-3889 ◽  
Author(s):  
Jian Wang ◽  
Yanzhi Yuan ◽  
Ying Zhou ◽  
Longhua Guo ◽  
Lingqiang Zhang ◽  
...  

2004 ◽  
Vol 22 (2) ◽  
pp. 177-183 ◽  
Author(s):  
Henning Hermjakob ◽  
Luisa Montecchi-Palazzi ◽  
Gary Bader ◽  
Jérôme Wojcik ◽  
Lukasz Salwinski ◽  
...  

2020 ◽  
Author(s):  
Diogo Borges Lima ◽  
Ying Zhu ◽  
Fan Liu

ABSTRACTSoftware tools that allow visualization and analysis of protein interaction networks are essential for studies in systems biology. One of the most popular network visualization tools in biology is Cytoscape, which offers a large selection of plugins for interpretation of protein interaction data. Chemical cross-linking coupled to mass spectrometry (XL-MS) is an increasingly important source for such interaction data, but there are currently no Cytoscape tools to analyze XL-MS results. In light of the suitability of Cytoscape platform but also to expand its toolbox, here we introduce XlinkCyNET, an open-source Cytoscape Java plugin for exploring large-scale XL-MS-based protein interaction networks. XlinkCyNET offers rapid and easy visualization of intra and intermolecular cross-links and the locations of protein domains in a rectangular bar style, allowing subdomain-level interrogation of the interaction network. XlinkCyNET is freely available from the Cytoscape app store: http://apps.cytoscape.org/apps/xlinkcynet and at https://www.theliulab.com/software/xlinkcynet.


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