Evidence map›Paper›PMID 25355808›Full record

ArticleGenome biology and evolution2014

The influence of selection for protein stability on dN/dS estimations.

Pouria Dasmeh, Adrian W R Serohijos, Kasper P Kepp, Eugene I Shakhnovich

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 60 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Aerolysin-like proteins fromFrontiers in fungal biology · 2026
    Article
  6. Leveraging FracMinHash Containment for GenomicbioRxiv : the preprint server for biology · 2025
    Article
  7. Article
  8. Article
  9. Evolution ofInternational journal of molecular sciences · 2025
    Article
  10. Article
  11. Article
  12. Stability and expression of SARS-CoV-2 spike-protein mutations.Molecular and cellular biochemistry · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Inferring the shape of global epistasis.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Article
  19. Review
  20. 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

4 authors at 3 institutions in 3 countries.

Pouria DasmehDepartment of Chemistry and Chemical Biology, Harvard University DTU Chemistry, Technical University of Denmark, Kongens Lyngby, Denmark Present address: Max Planck Institute of Immunobiology and Epigenetics, Stübeweg, Freiburg, Germany dasmeh@fas.harvard.edu serohij@fas.harvard.edu.
Adrian W R SerohijosDepartment of Chemistry and Chemical Biology, Harvard University dasmeh@fas.harvard.edu serohij@fas.harvard.edu.
Kasper P KeppDTU Chemistry, Technical University of Denmark, Kongens Lyngby, Denmark.
Eugene I ShakhnovichDepartment of Chemistry and Chemical Biology, Harvard University.
Harvard University · USMax Planck Institute of Immunobiology and Epigenetics · DETechnical University of Denmark · DK

Funding

Study of Biological Evolution of Structure and Function in ProteinsR01GM068670 · NIGMS · HARVARD UNIVERSITY · PI SHAKHNOVICH, EUGENE I · 2004 to 2020
$7.0M
NIGMS NIH HHS R01 GM068670
6 · The paper itself

Abstract

Understanding the relative contributions of various evolutionary processes-purifying selection, neutral drift, and adaptation-is fundamental to evolutionary biology. A common metric to distinguish these processes is the ratio of nonsynonymous to synonymous substitutions (i.e., dN/dS) interpreted from the neutral theory as a null model. However, from biophysical considerations, mutations have non-negligible effects on the biophysical properties of proteins such as folding stability. In this work, we investigated how stability affects the rate of protein evolution in phylogenetic trees by using simulations that combine explicit protein sequences with associated stability changes. We first simulated myoglobin evolution in phylogenetic trees with a biophysically realistic approach that accounts for 3D structural information and estimates of changes in stability upon mutation. We then compared evolutionary rates inferred directly from simulation to those estimated using maximum-likelihood (ML) methods. We found that the dN/dS estimated by ML methods (ωML) is highly predictive of the per gene dN/dS inferred from the simulated phylogenetic trees. This agreement is strong in the regime of high stability where protein evolution is neutral. At low folding stabilities and under mutation-selection balance, we observe deviations from neutrality (per gene dN/dS > 1 and dN/dS < 1). We showed that although per gene dN/dS is robust to these deviations, ML tests for positive selection detect statistically significant per site dN/dS > 1. Altogether, we show how protein biophysics affects the dN/dS estimations and its subsequent interpretation. These results are important for improving the current approaches for detecting positive selection.

Indexed as

Evolution, MolecularPhylogenyProteinsProtein StabilitySelection, GeneticProteinsdN/dSfolding stabilitymaximum likelihoodmolecular evolutionpositive selectionprotein evolution

Identifiers

PMID25355808
PMCPMC4224349
OpenAlexW2147082825

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.