Evidence map›Paper›PMID 18366735›Full record

ArticleBMC bioinformatics2008

A simple and fast heuristic for protein structure comparison.

David A Pelta, Juan R González, Marcos Moreno Vega

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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 5 papers.

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5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Benchmarking Methods of Protein Structure Alignment.Journal of molecular evolution · 2020
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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

David A PeltaModels of Decision and Optimization Research Group, Dept. of Computer Science and Artificial Intelligence, University of Granada, Spain. dpelta@decsai.ugr.es
Juan R González
Marcos Moreno Vega

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProtein structure comparison is a key problem in bioinformatics. There exist several methods for doing protein comparison, being the solution of the Maximum Contact Map Overlap problem (MAX-CMO) one of the alternatives available. Although this problem may be solved using exact algorithms, researchers require approximate algorithms that obtain good quality solutions using less computational resources than the formers.

resultsWe propose a variable neighborhood search metaheuristic for solving MAX-CMO. We analyze this strategy in two aspects: 1) from an optimization point of view the strategy is tested on two different datasets, obtaining an error of 3.5%(over 2702 pairs) and 1.7% (over 161 pairs) with respect to optimal values; thus leading to high accurate solutions in a simpler and less expensive way than exact algorithms; 2) in terms of protein structure classification, we conduct experiments on three datasets and show that is feasible to detect structural similarities at SCOP's family and CATH's architecture levels using normalized overlap values. Some limitations and the role of normalization are outlined for doing classification at SCOP's fold level.

conclusionWe designed, implemented and tested.a new tool for solving MAX-CMO, based on a well-known metaheuristic technique. The good balance between solution's quality and computational effort makes it a valuable tool. Moreover, to the best of our knowledge, this is the first time the MAX-CMO measure is tested at SCOP's fold and CATH's architecture levels with encouraging results.

Indexed as

AlgorithmsSoftwareAmino Acid SequenceMolecular Sequence DataPattern Recognition, AutomatedProtein ConformationProteinsSequence AlignmentSequence Analysis, ProteinProteins

Identifiers

PMID18366735
PMCPMC2335283

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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.