Evidence map›Paper›PMID 29482506›Full record

ArticleBMC bioinformatics2018

Effect of the sequence data deluge on the performance of methods for detecting protein functional residues.

Diego Garrido-Martín, Florencio Pazos

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Diego Garrido-MartínPresent address: Centre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, c/ Dr. Aiguader, 88, 08003, Barcelona, Spain.
Florencio PazosComputational Systems Biology Group, Systems Biology Program, National Centre for Biotechnology (CNB-CSIC), c/ Darwin, 3, 28049, Madrid, Spain. pazos@cnb.csic.es.

Funding

Spanish Ministry for Economy and Competitiveness SAF2016-78041-C2-2-R
6 · The paper itself

Abstract

backgroundThe exponential accumulation of new sequences in public databases is expected to improve the performance of all the approaches for predicting protein structural and functional features. Nevertheless, this was never assessed or quantified for some widely used methodologies, such as those aimed at detecting functional sites and functional subfamilies in protein multiple sequence alignments. Using raw protein sequences as only input, these approaches can detect fully conserved positions, as well as those with a family-dependent conservation pattern. Both types of residues are routinely used as predictors of functional sites and, consequently, understanding how the sequence content of the databases affects them is relevant and timely.

resultsIn this work we evaluate how the growth and change with time in the content of sequence databases affect five sequence-based approaches for detecting functional sites and subfamilies. We do that by recreating historical versions of the multiple sequence alignments that would have been obtained in the past based on the database contents at different time points, covering a period of 20 years. Applying the methods to these historical alignments allows quantifying the temporal variation in their performance. Our results show that the number of families to which these methods can be applied sharply increases with time, while their ability to detect potentially functional residues remains almost constant.

conclusionsThese results are informative for the methods' developers and final users, and may have implications in the design of new sequencing initiatives.

Indexed as

AlgorithmsAmino AcidsAmino Acid SequenceBinding SitesConserved SequenceMolecular Sequence AnnotationProteinsSequence AlignmentSequence Analysis, ProteinTime FactorsAmino AcidsProteinsConserved positionsFamily-dependent conserved positionFunctional residueFunctional subfamilySequence databaseSpecificity-determining position

Identifiers

PMID29482506
PMCPMC5827975

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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.