Evidence map›Paper›PMID 17683581›Full record

ArticleBMC bioinformatics2007

CLUSS: clustering of protein sequences based on a new similarity measure.

Abdellali Kelil, Shengrui Wang, Ryszard Brzezinski, Alain Fleury

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Article in BMC bioinformatics, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

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17citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

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  12. In silico characterization of thermostable lipases.Extremophiles : life under extreme conditions · 2011
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Abdellali KelilDépartement d'informatique, Faculté des Sciences, Université de Sherbrooke, Sherbrooke, QC, Canada. Abdellali.Kelil@USherbrooke.ca
Shengrui Wang
Ryszard Brzezinski
Alain Fleury

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe rapid burgeoning of available protein data makes the use of clustering within families of proteins increasingly important. The challenge is to identify subfamilies of evolutionarily related sequences. This identification reveals phylogenetic relationships, which provide prior knowledge to help researchers understand biological phenomena. A good evolutionary model is essential to achieve a clustering that reflects the biological reality, and an accurate estimate of protein sequence similarity is crucial to the building of such a model. Most existing algorithms estimate this similarity using techniques that are not necessarily biologically plausible, especially for hard-to-align sequences such as proteins with different domain structures, which cause many difficulties for the alignment-dependent algorithms. In this paper, we propose a novel similarity measure based on matching amino acid subsequences. This measure, named SMS for Substitution Matching Similarity, is especially designed for application to non-aligned protein sequences. It allows us to develop a new alignment-free algorithm, named CLUSS, for clustering protein families. To the best of our knowledge, this is the first alignment-free algorithm for clustering protein sequences. Unlike other clustering algorithms, CLUSS is effective on both alignable and non-alignable protein families. In the rest of the paper, we use the term "phylogenetic" in the sense of "relatedness of biological functions".

resultsTo show the effectiveness of CLUSS, we performed an extensive clustering on COG database. To demonstrate its ability to deal with hard-to-align sequences, we tested it on the GH2 family. In addition, we carried out experimental comparisons of CLUSS with a variety of mainstream algorithms. These comparisons were made on hard-to-align and easy-to-align protein sequences. The results of these experiments show the superiority of CLUSS in yielding clusters of proteins with similar functional activity.

conclusionWe have developed an effective method and tool for clustering protein sequences to meet the needs of biologists in terms of phylogenetic analysis and prediction of biological functions. Compared to existing clustering methods, CLUSS more accurately highlights the functional characteristics of the clustered families. It provides biologists with a new and plausible instrument for the analysis of protein sequences, especially those that cause problems for the alignment-dependent algorithms.

Indexed as

AlgorithmsEvolution, MolecularSoftwareAmino Acid SequenceCluster AnalysisMolecular Sequence DataMultigene FamilyProteinsSequence AlignmentSequence Analysis, DNASequence Homology, Amino AcidProteins

Identifiers

PMID17683581
PMCPMC1976428

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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.