Evidence map›Paper›PMID 23091608›Full record

ArticlePloS one2012

Accurate simulation and detection of coevolution signals in multiple sequence alignments.

Sharon H Ackerman, Elisabeth R Tillier, Domenico L Gatti

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Applications of sequence coevolution in membrane protein biochemistry.Biochimica et biophysica acta. Biomembranes · 2018
    Review
  6. Article
  7. COMPASS: the COMPletely Arbitrary Sequence Simulator.Bioinformatics (Oxford, England) · 2017
    Article
  8. Review
  9. Covariation Is a Poor Measure of Molecular Coevolution.Molecular biology and evolution · 2015
    Article
  10. Article
  11. Article
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

3 authors at 3 institutions in 2 countries.

Sharon H AckermanDepartment of Biochemistry and Molecular Biology, Wayne State University School of Medicine, Detroit, Michigan, United States of America.
Elisabeth R Tillier
Domenico L Gatti
Michigan United · USOntario Institute for Cancer Research · CAWayne State University · US

Funding

BIOGENESIS OF THE YEAST MITOCHONDRIAL ATPASE COMPLEXR01GM048157 · NIGMS · WAYNE STATE UNIVERSITY · PI ACKERMAN, SHARON H. · 1992 to 2006
$1.3M
Structure, mechanism and evolution of KDO8P synthaseR01GM069840 · NIGMS · WAYNE STATE UNIVERSITY · PI GATTI, DOMENICO L · 2004 to 2007
$1.1M
NIGMS NIH HHS GM48157NIGMS NIH HHS GM69840NIGMS NIH HHS R01 GM048157NIGMS NIH HHS R01 GM069840
6 · The paper itself

Abstract

backgroundWhile the conserved positions of a multiple sequence alignment (MSA) are clearly of interest, non-conserved positions can also be important because, for example, destabilizing effects at one position can be compensated by stabilizing effects at another position. Different methods have been developed to recognize the evolutionary relationship between amino acid sites, and to disentangle functional/structural dependencies from historical/phylogenetic ones. METHODOLOGY/PRINCIPAL

findingsWe have used two complementary approaches to test the efficacy of these methods. In the first approach, we have used a new program, MSAvolve, for the in silico evolution of MSAs, which records a detailed history of all covarying positions, and builds a global coevolution matrix as the accumulated sum of individual matrices for the positions forced to co-vary, the recombinant coevolution, and the stochastic coevolution. We have simulated over 1600 MSAs for 8 protein families, which reflect sequences of different sizes and proteins with widely different functions. The calculated coevolution matrices were compared with the coevolution matrices obtained for the same evolved MSAs with different coevolution detection methods. In a second approach we have evaluated the capacity of the different methods to predict close contacts in the representative X-ray structures of an additional 150 protein families using only experimental MSAs. CONCLUSIONS/SIGNIFICANCE: Methods based on the identification of global correlations between pairs were found to be generally superior to methods based only on local correlations in their capacity to identify coevolving residues using either simulated or experimental MSAs. However, the significant variability in the performance of different methods with different proteins suggests that the simulation of MSAs that replicate the statistical properties of the experimental MSA can be a valuable tool to identify the coevolution detection method that is most effective in each case.

Indexed as

Evolution, MolecularSequence AlignmentAmino Acid SequenceComputational BiologyComputer SimulationMolecular Sequence DataProteinsReproducibility of ResultsProteins

Identifiers

PMID23091608
PMCPMC3473043
OpenAlexW2047437886

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.