Evidence map›Paper›PMID 18957106›Full record

ArticleBMC systems biology2008

From protein interactions to functional annotation: graph alignment in Herpes.

Michal Kolár, Michael Lässig, Johannes Berg

Abstract read
In one paragraph

Article in BMC systems biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Michal KolárInstitut für Theoretische Physik, Universität zu Köln, Zülpicher Strasse 77, 50937 Köln, Germany. kolarmi@thp.uni-koeln.de
Michael Lässig
Johannes Berg

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSequence alignment is a prolific basis of functional annotation, but remains a challenging problem in the 'twilight zone' of high sequence divergence or short gene length. Here we demonstrate how information on gene interactions can help to resolve ambiguous sequence alignments. We compare two distant Herpes viruses by constructing a graph alignment, which is based jointly on the similarity of their protein interaction networks and on sequence similarity. This hybrid method provides functional associations between proteins of the two organisms that cannot be obtained from sequence or interaction data alone.

resultsWe find proteins where interaction similarity and sequence similarity are individually weak, but together provide significant evidence of orthology. There are also proteins with high interaction similarity but without any detectable sequence similarity, providing evidence of functional association beyond sequence homology. The functional predictions derived from our alignment are consistent with genomic position and gene expression data.

conclusionOur approach shows that evolutionary conservation is a powerful filter to make protein interaction data informative about functional similarities between the interacting proteins, and it establishes graph alignment as a powerful tool for the comparative analysis of data from highly diverged species.

Indexed as

Evolution, MolecularHerpesvirus 3, HumanHerpesvirus 8, HumanOpen Reading FramesProtein BindingReproducibility of ResultsSequence AlignmentSequence Homology, Amino AcidViral ProteinsViral Proteins

Identifiers

PMID18957106
PMCPMC2607256

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LicenceCC BY
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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.