Evidence map›Paper›PMID 26458889›Full record

ArticleBioinformatics (Oxford, England)2016

A multi-objective optimization approach accurately resolves protein domain architectures.

J S Bernardes, F R J Vieira, G Zaverucha, A Carbone

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

19 citing papers in PubMed.

  1. Article
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  7. Protein domain identification methods and online resources.Computational and structural biotechnology journal · 2021
    Review
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  17. Domain prediction with probabilistic directional context.Bioinformatics (Oxford, England) · 2017
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

J S BernardesSorbonne Universités, UPMC Univ-Paris 6, CNRS, UMR 7238, Laboratoire de Biologie Computationnelle et Quantitative, 15 rue de l'Ecole de Médecine, 75006 Paris.
F R J VieiraCNRS, UMR 7606, Laboratoire d'Informatique de Paris 6, 75005 Paris, France and COPPE-UFRJ, Programa de Engenharia de Sistemas e Computação, Rio de Janeiro, Brazil.
G ZaveruchaCOPPE-UFRJ, Programa de Engenharia de Sistemas e Computação, Rio de Janeiro, Brazil.
A CarboneSorbonne Universités, UPMC Univ-Paris 6, CNRS, UMR 7238, Laboratoire de Biologie Computationnelle et Quantitative, 15 rue de l'Ecole de Médecine, 75006 Paris, Institut Universitaire de France, 75005 Paris.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationGiven a protein sequence and a number of potential domains matching it, what are the domain content and the most likely domain architecture for the sequence? This problem is of fundamental importance in protein annotation, constituting one of the main steps of all predictive annotation strategies. On the other hand, when potential domains are several and in conflict because of overlapping domain boundaries, finding a solution for the problem might become difficult. An accurate prediction of the domain architecture of a multi-domain protein provides important information for function prediction, comparative genomics and molecular evolution.

resultsWe developed DAMA (Domain Annotation by a Multi-objective Approach), a novel approach that identifies architectures through a multi-objective optimization algorithm combining scores of domain matches, previously observed multi-domain co-occurrence and domain overlapping. DAMA has been validated on a known benchmark dataset based on CATH structural domain assignments and on the set of Plasmodium falciparum proteins. When compared with existing tools on both datasets, it outperforms all of them. AVAILABILITY AND IMPLEMENTATION: DAMA software is implemented in C++ and the source code can be found at http://www.lcqb.upmc.fr/DAMA. CONTACT: juliana.silva_bernardes@upmc.fr or alessandra.carbone@lip6.fr SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

AlgorithmsProtein Structure, TertiaryGenomicsMolecular Sequence AnnotationPlasmodium falciparumProtozoan ProteinsSequence Analysis, ProteinSoftwareProtozoan Proteins

Identifiers

PMID26458889
PMCPMC4734041

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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.