Evidence map›Paper›PMID 18547430›Full record

ArticleBMC bioinformatics2008

Discovering functional interaction patterns in protein-protein interaction networks.

Mehmet E Turanalp, Tolga Can

Abstract read
In one paragraph

Article in BMC bioinformatics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Identification of MFS proteins in sorghum using semantic similarity.Theory in biosciences = Theorie in den Biowissenschaften · 2013
    Article
  4. Article
  5. Identification of salt treated proteins in sorghum using gene ontology linkage.Physiology and molecular biology of plants : an international journal of functional plant biology · 2012
    Article
  6. Article
4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Mehmet E TuranalpDepartment of Computer Engineering, Selcuk University, Alaaddin Keykubat Kampusu, 42075 Selcuklu, Konya, Turkey. eturanalp@selcuk.edu.tr
Tolga Can

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn recent years, a considerable amount of research effort has been directed to the analysis of biological networks with the availability of genome-scale networks of genes and/or proteins of an increasing number of organisms. A protein-protein interaction (PPI) network is a particular biological network which represents physical interactions between pairs of proteins of an organism. Major research on PPI networks has focused on understanding the topological organization of PPI networks, evolution of PPI networks and identification of conserved subnetworks across different species, discovery of modules of interaction, use of PPI networks for functional annotation of uncharacterized proteins, and improvement of the accuracy of currently available networks.

resultsIn this article, we map known functional annotations of proteins onto a PPI network in order to identify frequently occurring interaction patterns in the functional space. We propose a new frequent pattern identification technique, PPISpan, adapted specifically for PPI networks from a well-known frequent subgraph identification method, gSpan. Existing module discovery techniques either look for specific clique-like highly interacting protein clusters or linear paths of interaction. However, our goal is different; instead of single clusters or pathways, we look for recurring functional interaction patterns in arbitrary topologies. We have applied PPISpan on PPI networks of Saccharomyces cerevisiae and identified a number of frequently occurring functional interaction patterns.

conclusionWith the help of PPISpan, recurring functional interaction patterns in an organism's PPI network can be identified. Such an analysis offers a new perspective on the modular organization of PPI networks. The complete list of identified functional interaction patterns is available at http://bioserver.ceng.metu.edu.tr/PPISpan/.

Indexed as

AlgorithmsModels, BiologicalArtificial IntelligenceComputer SimulationPattern Recognition, AutomatedProtein Interaction MappingProteomeSignal TransductionProteome

Identifiers

PMID18547430
PMCPMC2442100

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.